sodininkystë ir darþininkystë 25(3)

Transcription

sodininkystë ir darþininkystë 25(3)
LIETUVOS SODININKYSTËS IR DARÞININKYSTËS INSTITUTO
IR LIETUVOS ÞEMËS ÛKIO UNIVERSITETO MOKSLO DARBAI
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF
AGRICULTURE
SODININKYSTË IR DARÞININKYSTË
25(3)
Eina nuo 1983 m.
Published since 1983
Babtai - 2006
Redaktoriø kolegija
Editorial Board
Doc. dr. Èeslovas BOBINAS - pirmininkas (LSDI, biomedicinos mokslai, agronomija),
prof. habil. dr. Pavelas DUCHOVSKIS (LSDI, biomedicinos mokslai, agronomija),
dr. Edite KAUFMANE (Latvija, Dobelës sodo augalø selekcijos stotis, biomedicinos
mokslai, biologija). dr. Aleksandras KMITAS (LÞÛU, biomedicinos mokslai,
agronomija), dr. Laimutis RAUDONIS (LSDI, biomedicinos mokslai, agronomija),
prof. habil. dr. Vidmantas STANYS (LSDI, biomedicinos mokslai, agronomija),
prof. habil. dr. Andrzej SADOWSKI (Varðuvos ÞÛA, biomedicinos mokslai,
agronomija), dr. Audrius SASNAUSKAS (LSDI, biomedicinos mokslai, agronomija),
prof. habil. dr. Algirdas SLIESARAVIÈIUS (LÞÛU, biomedicinos mokslai,
agronomija).
Redakcinë mokslinë taryba
Editorial Scientific Council
Doc. dr. Èeslovas BOBINAS - pirmininkas (Lietuva),
prof. habil. dr. Pavelas DUCHOVSKIS (Lietuva), dr. Kalju KASK (Estija), dr. Edite
KAUFMANE (Latvija), prof. habil. dr. Zdisùaw KAWECKI (Lenkija), prof. habil.dr.
Albinas LUGAUSKAS (Lietuva), habil. dr. Maria LEJA (Lenkija), prof. habil. dr. Lech
MICHALCZUK (Lenkija), prof. habil. dr. Andrzej SADOWSKI (Lenkija),
dr. Audrius SASNAUSKAS (Lietuva), prof. dr. Ala SILAJEVA (Ukraina), prof. habil.
dr. Algirdas SLIESARAVIÈIUS (Lietuva), prof. habil. dr. Vidmantas STANYS (Lietuva),
prof. dr. Viktor TRAJKOVSKI (Ðvedija).
Redakcijos adresas:
Address of the Editorial Office:
Lietuvos sodininkystës ir darþininkystës institutas
LT-54333 Babtai, Kauno r.
Tel. (8~37) 555 210
Faksas: (8~37) 555 176
El. paðtas [email protected]
Lithuanian Institute of Horticulture
LT-54333 Babtai, Kaunas district, Lithuania
Phone: +370-37-555-210
Telefax: +370-37-555-176
E-mail: [email protected]
Leidinio adresas internete www.lsdi.lt
Leidinys cituojamas CAB Internacional ir VINITI duomenø bazëse
© Lietuvos sodininkystës ir darþininkystës institutas, 2006
© Lietuvos þemës ûkio universitetas, 2006
2
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 3–12.
APPLE AND PEAR ROOTSTOCK RESEARCH
IN LITHUANIA
Darius KVIKLYS
Lithuanian Institute of Horticulture LT–54333 Babtai, Kaunas distr.,
Lithuania. E-mail: [email protected]
The paper presents ongoing apple and pear rootstock trials at the Lithuanian Institute
of Horticulture. Rootstock research projects are established in following directions:
rootstock and location interaction (Baltic fruit rootstock studies where Byelorussian,
Estonian, Latvian, Lithuanian and Polish research institutions are involved); budding
high effect on rootstock performance; interstock trials; rootstock effect on fruit quality,
ripening time and fruit storage; rootstock and tree training system; virus status of apple
planting material on different rootstocks (international trial with Applied Plant Research,
Netherlands); rootstock and soil sickness in nursery; rootstock resistance to Phytophtora;
rootstock response to irrigation; rootstock effect on tree physiological parameters and
flower physiology; rootstock effect on tree nutrition; rootstock and dry matter
accumulation; genetic engineering of Cydonia oblonga rootstocks. Following apple
rootstocks are included in different research projects: M and MM series – M.9, M.26,
MM.106; P series – P 2, P 22, P 14, P 59, P 60, P 61, P 62, P 66, P 67; B series – B.9, B.118,
B.136, B.396, B.491, other rootstocks as PB.4, Bulboga, York 9, Pure 1 and Antonowka
seedlings. Following pear rootstocks are included in different research projects: quinces
– QA, QC, Sydo, BA-29, S 1, K.11, K.16, K.19, 1.2, pears – Pyrodwarf, OHF333, Mostbirne,
Kazrausu. 14 scientists from Orchard technology department, Department of Genetics
and Biotechnology of Orchard Plants, Plant protection laboratory, Laboratory of
Biochemistry and Technology, Laboratory of Plant Physiology are involved in rootstock
research.
trial.
Key words: Cydonia x oblonga, Malus x domestica, Pyrus x communis, rootstock,
Introduction. Scientifically based rootstock research in Lithuania was started
at the Vytënai Horticultural Research Station (in 1987 reorganized into Lithuanian
Institute of Horticulture) in 1960 (Kviklys, 1977). Apple rootstock research developed
into different directions: propagation, nursery trials, rootstock vigour, winter hardiness,
rootstock use as interstems, rootstock effect on fruit quality, storage capacity, ripening
time, etc. (Kviklys, 1977, 1992; Ðvirinas, 1986; Ðumskis, 1986a, 1986b, Kviklys et
al., 1988; Kviklys, Kviklienë, 2002; Kviklys, 2004). During 1963–2002 more than 40
vegetative rootstocks and 20 seedling rootstocks were evaluated in the orchard for
3
their productivity and effect on fruit quality (Kviklienë, Kviklys, 2001; 2004;
Duchovskis et al., 2000; Kviklys et al., 1999, 2000; Uselis, 2002, 2003, 2004, 2005).
After long term of evaluation rootstocks MM.106 and B.118, semi-dwarf M.26, P 60
and B.396, dwarf M.9 and P 22 were recommended for propagation and growing on
commercial scale (Kviklys, 2002).
At this moment rootstock research is being developed in following directions:
rootstock and location interaction; budding high effect on rootstock performance;
interstock trials; rootstock effect on fruit quality, ripening time and fruit storage;
rootstock and tree training system; virus status of apple planting material on different
rootstocks; rootstock and soil sickness in nursery; rootstock resistance to
Phytophthora cactorum; rootstock response to irrigation; rootstock effect on tree
physiological parameters; rootstock effect on tree nutrition; rootstock and dry matter
accumulation; genetic engineering of Cydonia oblonga rootstocks.
The aim of our work is to present ongoing trials and achievements of rootstock
research projects at the Lithuanian Institute of Horticulture.
Material and methods. All rootstock trials in the orchard are established in
four-five replications with 3–5 trees in each. Replications are randomised. Variance
analyses are performed and criteria are chosen according to trial schemes.
T r e e v i g o u r c o n t r o l. As a measure for the tree vigour control trunk
circumference is measured annually; total shoot length is measured first two-three
years after trial establishment; tree height is measured until it reaches technological
allowed height. Additional measurements, as mean shoot length, canopy volume,
number of buds on the shoot, are taken according to trial scheme.
Y i e l d a n d p r o d u c t i v i t y. Yield per tree and per hectare are the main
measurements. Tree productivity is counted as kg cm-2 of trunk cross sectional
area.
F r u i t q u a l i t y , h a r v e s t t i m e. From each replication 100 fruits are
weighed and sized in 5 mm intervals. Fruit colouring is expressed by percentage of
red colour covering fruit surface. Ten fruits from each replication are taken for
laboratory measurements. Fruit firmness is measured with an Effegi penetrometer.
Starch conversion is estimated after treatment with 0.1n iodine and potassium iodine
solution (scale 1–10). Concentration of soluble solids is determined with refractometer.
Maturity index is calculated as F/RS, where F – firmness, R – concentration of
soluble solids, S – starch conversion.
Flowering time, T-phase, days after full bloom are counted for harvest time
evaluation.
Natural mass loss, fruit rots, storage diseases, transpiration is recorded for
storage trials.
H o r m o n e s. Analyses of gibberellic acid (GA3), indolyl-3-acetic acid (IAA),
abscisic acid (ABA) and zeatin are performed using HP 1050 Series liquid
chromatography system with variable wavelength UV-VIS detector (Agilent
Technologies, Waldbronn, Germany). Intersil ODS-2 column (150 x 4.6 mm2) (Alltech,
Deerfield, USA) was used for phytohormones separation. Mobile phase: 45% methanol
containing 1% acetic acid. Flow rate: 1 mL/min. The wavelengths of 254 nm for
GA3 and ABA detection, 270 nm for zeatin and 280 nm for IAA detection were set.
4
P i g m e n t s. Total chlorophyll and carotenoid content in green mass is
determined in 100% acetone extracts using spectrophotometrical Wettstein method
[13]. Spectrophotometer – Genesys 6 (ThermoSpectronic, USA).
S u g a r s. Carbohydrate samples are prepared by grinding ~ 1g of fresh weight
(FW) material and extracted with 4 mL hot bidistiled water. After 24 h extract is
filtered through cellulose and membrane (pore diameter 0.2 µm) filters.
Chromatographic analysis was carried-out using Shimadzu 10A HPLC system with
refraction index detector (Shimadzu, Japan) and Adsorbosil NH2 – column (150 mm
x 4.6 mm; Alltech, USA). Mobile phase: 75% acetonitrile. Flow rate: 1 m/min.
M o r p h o p h y s i o l o g i c a l analysis of buds is performed according to
F. Kuperman methodology. Bud development is analyzed by microscope and
organogenesis stage is established.
Resistance to Phytophthora cactorum (Lebert & Cohn) Schroeter. In vegetation
trial isolates of Phytophthora cactorum are tested on one year old apple rootstocks
grown in pots in a greenhouse. Inoculations are made via insertion of small agar
plugs from actively growing cultures into bark flaps in two sides. Length of necrosis
is measured after five weeks after inoculation. Total plant weight, fresh and dry
root, leaf, trunk weight are measured.
In laboratorial trial current season shoots are used. They are inoculated mycelia
disks of Phytophthora cactorum, taken from seven-day-old culture grown on PDA.
Basal and middle rootstock shoot parts are incubated on moist blotting paper in foilcovered polystyrene boxes. Length of necrosis is measured after 3 and 8 days of
incubation.
D r o u g h t s t r e s s. Biometric measurements are done at the end of
experiment. Total plant weight, fresh and dry root, leaf, trunk weight are measured.
Leaf area is measured by Leaf area meter WinDias (U.K).
Budding height trials. Trial with P 60 and B.396 rootstocks budded at 5, 10, 20
and 30 cm planted in the spring of 2000. Planting distances – 4 x 1.5 m.
Trial with M.9, M.26, P 22, P 59 rootstocks budded at 5, 10, 20 and 30 cm
planted in the spring of 2002. Planting distances – 4 x 1.5 m for M.26 and 4x1 m. for
M.9, P 22, P 59.
‘Baltic fruit rootstocks studies’. Location effect on rootstock performance.
Trial with apple cv. ‘Auksis’ on P 22, P 2, M.9, B.9, Pure 1, B.491, B.146, York 9,
B.396, P 60, M.26 and Bulboga rootstocks planted in the spring of 2001. Planting
distances – 4 x 1.5 m. Under the same scheme trials were established at Babtai,
Lithuanian Institute of Horticulture (Lithuania), Pure Horticultural Research Centre
(Latvia), Polli Research Centre of the Institute of Agricultural and Environmental
Sciences of the Estonian University of Life Sciences (Estonia), and Pruzany, Brest
Agricultural Experimental Station (Byelorussia).
Trial with apple cv. ‘Beloruskoje malinovoje’ on P 22, M.9, B.9, Pure 1, B.146,
B.396, P 60, M.26 and Bulboga rootstocks planted in the spring of 2001. Planting
distances – 4 x 1.5 m. Under the same scheme trials were established at Lithuanian
Institute of Horticulture, Pure Horticultural Research Centre, Polli Research Centre,
and Brest Agricultural Experimental Station.
5
Trial with pear cv. ‘Suvenir’ on Quince BA29, QA, QC, Pyrus Pyrodwarf,
Pyrus OHF333, Pyrus Kirchensaller Mostbirne, and Pyrus Kazrausu planted in the
spring of 2001. Planting distances – 4 x 3 m for seedling rootstocks and 4 x 2 m for
clonal rootstocks. Under the same scheme trials were established at Lithuanian Institute
of Horticulture, Pure Horticultural Research Centre, Polli Research Centre, and Brest
Agricultural Experimental Station.
Trial with apple cvs. ‘Auksis’ and ‘Ligol’ on B.396, B.9, PB-4, Pure 1, M.9,
M.26, P 22, P 59, P 61, P 62, P 66, P 67 in the spring of 2005. Planting distances –
4 x 1.5 m. Under the same scheme trials were established at Lithuanian Institute of
Horticulture, Pure Horticultural Research Centre, Polli Research Centre, and
Skierniewice, Research Institute of Pomology and Floriculture (Poland).
Interstock trial includes rootstocks B.9, P 22, B.396, 3-3-72, apple cvs.
‘Summered’, ‘Kaunis’, ‘Lietuvos pepinas’, columnar apple 109 and planted in the
autumn of 2002. Planting distances – 4 x 1.5 m.. Interstock length 30 cm, rootstock
B.396.
Virus status of planting material. International trial planted in the spring of 2003
together with Applied Plant Research, Research Unit Fruit, Randwijk, Netherlands.
Cvs. ‘Sampion’ and ‘Jonagold decosta’ on M.9 and M.26 rootstocks. Planting distances
– 3 x 1 for M.9 and 3 x 1.5 for M.26. Virus free and not tested material is evaluated.
Replant trial in the nursery established in 2005. Cvs. ‘Auksis’ and ‘Sampion’
budded on M.9, M.26, MM.106, P 2, P 22, P 59, P 60, B.396, B.118, Antonowka
seedling rootstocks and planted in fresh soil and at the place where apple stoolbeds
were cultivated for 10 years.
Rootstock and orchard constructions. Trial with cv. ‘Auksis’ on P 22 and P 60
rootstocks planted in 2001. Different planting schemes and tree training systems are
evaluated.
Trial with cv. ‘Rubin’ on P 22 and P 60 rootstocks planted in 2001. Time and
crown training systems are evaluated.
Rootstock and planting distances. Trial with cv. ‘Ligol’ on P 22, P 2 and P 60
rootstocks planted in 1999. Different planting schemes are evaluated.
Trial with cv. ‘Lodel’ on M.26, P 2 and P 60 rootstocks planted in 1999. Different
planting schemes are evaluated.
Trial with cv. ‘Delikates’ on M.26, MM.106 and seedling rootstocks planted in
1999. Different planting schemes are evaluated.
Rootstock effect on tree physiology. Trial started in 2004 with cv. ‘Auksis’ on
P 22, P 2, M.9, B.9, Pure 1, B.491, B.146, York 9, B.396, P 60, and M.26 rootstocks.
Drought stress trial established ex-situ in 2005 with M.9, M.26, MM.106, P 2,
P 22, P 59, P 60, B.396, B.118, Antonowka seedling rootstocks. Three soil moisture
regimes are created: 20–30 kPa, 40–50 kPa, and >70 kPa.
Rootstock resistance to Phytophthora cactorum trials established ex-situ and in
laboratory in 2006 with M.9, MM.106, P 60, B.396 and B.118 rootstocks.
Rootstock effect on fruit quality and harvest time. Trial with apple cv. ‘Auksis’
on P 22, P 2, M.9, B.9, Pure 1, B.491, B.146, York 9, B.396, P 60, M.26 and Bulboga
rootstocks started in 2004.
6
Trial with apple cv. ‘Auksis’ on B.396 and P60 budded at 5, 10, 20 and 30 cm
started in 2004.
Trial with pear cv. ‘Conference’ on QA, QC, Sydo, QS1, K.16, K.11, 1.2
rootstocks and Pyrus x communis seedlings started in 2000.
Rootstock choice to columnar apple varieties. 24 columnar apple selections
from the breeding program at the Lithuanian Institute of Horticulture are tested on
P 60, B.396, M.26, MM.106, B.118 and seedling rootstocks.
Genetic engineering of Cydonia oblonga rootstocks. Quince rootstocks K.11,
K.16 and K.19 from Lithuanian rootstock breeding program are included. RolB gene
(~ 800 bp) was isolated from Agrobacterium rhizogenes in PCR with rolB5kodrolB3kod primers. Binary constructs basing on pART27 and pNOV2819 plasmids
and containing rolB gene under own promoter sequence, 35S CaMV, and stressinduced PR promoter were prepared and used to transform quince using
A. tumefaciens.
Results. Some published and more important preliminary results of ongoing
rootstock trials at the Lithuanian Institute of Horticulture are presented.
‘B a l t i c f r u i t r o o t s t o c k s s t u d i e s ’ . L o c a t i o n e f f e c t o n
r o o t s t o c k p e r f o r m a n c e. The strongest tree growth of cv. ‘Auksis’ was
recorded in Lithuania and Byelorussia. The highest yields were obtained in Lithuania.
All tested rootstocks according growth vigour control can be grouped in the following
way: less vigour than M.9 – P 22, the same as M.9 – Pure 1, B.396, York 9, P.60, B.9
and P 2, between M.9 and M.26 – B.491, the same or more vigorous as M.26 –
Bulboga and B.146. Trees on rootstocks Pure 1 gave the highest cumulative yield
and were the most efficient although there was no significant difference in cumulative
fertility index with trees growing on rootstocks P 22, P 2, M.9, B.9 and York 9. The
least efficient were trees on rootstocks Bulboga and B.146. Rootstock and location
interaction was recorded for B.491 and P.60 in growth vigour control, York 9 in total
yield, and B.9 in yield efficiency (Kviklys et al., 2006).
The evaluation of vegetative growth showed that the most vigorous trees of
apple cv. ‘Belorusskoye Malinovoye’ were on rootstock Bulboga, followed by B.146,
M.26, P 60, B.396, M.9, B.9 and Pure 1. The smallest trees were on P 2. Highest
cumulated yield was harvested from the trees on rootstocks M.26 and B.396, the
smallest – on P 22 and B.9. The highest yield efficiency (kg cm-2 TCSA) was observed
on Pure 1 and B.9 rootstocks, the smallest – on B.146 and M.26. These results were
observed in all trials in all four scientific institutions, although some differences were
noted (Bite et al., 2006).
In Lithuania pear trees grew more vigorously than in two other localities. The
trees on the QC were founded to be smaller and the trees on Pyrodwarf. In Latvia, the
trees on all Pyrus rootstocks were more vigorous than these on Cydonia rootstocs. In
Estonia, the trees on Pyrodwarf and OHF 333 were found to be weaker than these on
Cydonia rootstocks. The first crop in Lithuania appeared in the fourth year after planting
only on Cydonia and Pyrodwarf rootstocks. In Estonia and Latvia, the first crop appeared
in the fifth year on all rootstocks due to the entire killing of flowers in the fourth year
by spring night frosts; the first crop was bigger on Cydonia rootstocks. In Lithuania,
the fruit mass was bigger on OHF 333 than that of BA 29 (Haak et al., 2006).
7
R o o t s t o c k e f f e c t o n f r u i t q u a l i t y. High yielding trees on dwarf
rootstock Pure 1 have the smallest fruits. Largest fruits were on strong growing
Bulboga, B.146 and dwarf rootstock M.9. Pure 1 and P 22 determined better fruit
colouring. Fruits on Bulboga were firmer, and these on rootstock P 2 – softer. P 2
determined higher content of soluble solids (Kviklienë, Kviklys, 2006).
The biggest ‘Conference’ fruit weight were from trees on rootstock QS1, K.11
and K.16. These rootstocks and QA increased fruit diameter. Pyrus x communis
seedlings negatively effected fruit mass. ‘Conference’ fruits on the Pyrus x communis
seedling rootstock were firmer at harvest and as well as QS1 and 1.2 rootstocks had
higher starch content. There were no rootstock influence on the soluble solids content
and maturity indices among Cydonia oblonga rootstocks (Kviklys, Kviklienë, 2005a).
R o o t s t o c k e f f e c t o n f r u i t m a t u r i t y. The maturity index indicated
that ‘Auksis’ apples were more mature from trees on rootstock Pure 1. Rootstock
Bulboga caused later ripening of apples.
The maturity indices indicated that ‘Conference’ pears were more mature from
trees on Cydonia oblonga rootstocks (Kviklys, Kviklienë, 2004).
R o o t s t o c k s c h o i c e f o r c v. ‘C o n f e r e n c e’. Rootstock 1.2
significantly reduced growth of a pear tree (stem diameter and total shoot length
during the first two years), whereas trees on Sydo and seedling rootstocks had the
strongest growth. Significant differences of stem diameter were not established
between other tested rootstocks after five years in the orchard. Quince MC, Sydo,
K11 and K16 were the earliest to start cropping. Trees grafted onto them started to
yield in the second year after planting. The highest cumulative yield was obtained on
Quince MC followed by Sydo. Other rootstocks gave statistically lower yields.
Significant differences were not found among Quince MA, K.16, K.11 and S1. The
lowest yield was on 1.2 and Pyrus x communis seedling rootstocks (Kviklys, 2005).
V i r u s s t a t u s o f p l a n t i n g m a t e r i a l. Virus free trees had stronger
vegetative growth (total shoot length and stem diameter) at planting year than not
tested ones. During second and third year in the orchard vegetative and generative
development of apple trees and fruit weight did not depend on health status of planting
material. During the second season virus free trees of cv. ‘Ðampion’ had higher
yield, but lower growth, when not tested trees – lower yield and stronger growth.
During the third year opposite tendencies were established. Correlation between
vegetative growth and generative development of cv. ‘Jonagold’ was not established.
Health status of planting material had no effect on scab incidence on leaves and
fruits. Not tested trees were more sensitive to bark diseases (Kviklys, Stankienë,
2005).
B u d d i n g h e i g h t. The differences among rootstocks were recorded already
in the second year. Trees on P 60 grew stronger than on B.396. Stronger growth of
trees was recorded at lower budding height too. Trees planted at the height of 0 and
10 cm significantly differed from trees at the height of 20 and 30 cm in total shoot
growth, stem diameter and tree height. First crop was the same on both rootstocks
and there were no significant difference between budding height. In following two
years significant differences occurred for both rootstocks and budding height.
Rootstock B.396 gave higher yield and trees on it were smaller. Influence of budding
8
height on crop load differed between years and rootstocks. Significant differences
were found with B.396 budded at different height. Less pronounced differences
were with P 60 rootstock. Trees, which budded higher, had smaller stem diameter.
Apple fruit weight did not depend on budding height (Kviklys, Kviklienë, 2005b).
G e n e t i c e n g i n e e r i n g o f C y d o n i a o b l o n g a r o o t s t o c k s. The
aim is to transform quince rootstocks to increase their rooting ability. RolB gene was
isolated from Agrobacterium rhizogenes. 1992 explants derived from clones K.1,
K.16 and K.19 were transformed using A. tumefaciens (Raþanskienë et al., 2006).
Transgenic plants were obtained with good rooting ability. Root morphology was
typical to plants transformed with rolB gene.
Discussion. The choice of rootstocks depends mostly on climatic conditions,
which are usually more unsatisfactory in northern countries. The length of the
vegetation period, sum of temperatures and rain precipitations have significant effects
on the rootstock performance. The vegetation period in Lithuania is shorter than in
other European countries and the sum of temperatures is also lower. Winter could be
a limiting factor of growing sensitive apple and pear rootstocks. Apple and pear
rootstocks are released in different countries and have their own quality parameters
and often exhibit unequal performance in different countries (Wertheim, 1998), mainly
due to ecological conditions. Therefore rootstock research is relevant in Lithuania in
order to develop commercial fruit growing and scientific knowledge.
At the Lithuanian Institute of Horticulture 14 research workers from Orchard
technology department, Department of Genetics and Biotechnology of Orchard Plants,
Plant protection laboratory, Laboratory of Biochemistry and Technology, Laboratory
of Plant Physiology are involved in rootstock research. Research collaboration and
mutual rootstock trials take place with Applied Plant Research, Research Unit Fruit,
Randwijk, (Netherlands), Research Institute of Pomology and Floriculture,
Skierniewice, (Poland), Pure Horticultural Research Centre (Latvia), Polli Research
Centre of the Institute of Agricultural and Environmental Sciences of the Estonian
University of Life Sciences (Estonia), and Brest Agricultural Experimental Station,
Pruzany (Byelorussia) (Bite et al., 2004; 1999).
24 apple and pear rootstock research projects are being carried out at the
Lithuanian Institute of Horticulture in 2006: 15 projects at the Orchard Technology
Department, 2 projects together at the Orchard Technology Department and
Laboratory of Plant Physiology, 2 projects together at the Orchard Technology
Department and Plant protection laboratory, 1 project together at the Orchard
Technology Department and Department of Genetics and Biotechnology of Orchard
Plants, 1 project together at the Orchard Technology Department and Laboratory of
Biochemistry and Technology, 2 projects at the Department of Genetics and
Biotechnology of Orchard Plants, 1 project together at the Department of Genetics
and Biotechnology of Orchard Plants and Laboratory of Plant Physiology.
Following apple and pear rootstocks are included in different research projects:
M and MM series – M.9, M.26, MM.106; P series – P 2, P 22, P 14, P 59, P 60, P 61,
P 62, P 66, P 67; B series – B.9, B.118, B.136, B.396, B.491, other rootstocks as
PB.4, Bulboga, York 9, Pure 1 and Antonowka seedlings; quinces – QA, QC, Sydo,
BA-29, S 1, K.11, K.16 and 1.2; pears – Pyrodwarf, OHF333, Mostbirne, Kazrausu.
9
In 2003–2005 research workers of the Lithuanian Institute of Horticulture have
published 25 scientific publications on apple and pear rootstock research.
Gauta
2006 06 06
Parengta spausdinti
2006 07 25
References
1. B i t e A., L e p s i s J., K v i k l y s D., H a a k E., L u k u t T.
Results of apple rootstock testing with cultivar ‘Belorusskoye malinovoye‘ in the frame of
project "Baltic fruit rootstock studies" // Sodininkystë ir darþininkystë. 2006. 25(3)
(in press).
2. B i t e A., K v i k l y s D., U n i v e r T., L u k u t T. The beginning of
the project “Baltic fruit rootstock studies” // Acta Horticulturae. 2004. 658 (1). P. 437–440.
3. B i t e A., K v i k l y s D., H a a k E., L u k u t T. International project
"Baltic fruit rootstock studies" // Apple rootstocks for intensive orchards. Warszawa.
1999. P. 17–19.
4. D u c h o v s k i s P., K v i k l y s D., K a w e c k i Z., P e t r o n i s P.,
K v i k l i e n ë N. Impact of rootstock and irrigation on apple bud differentiation and
flowering initiation // Sodininkystë ir darþininkystë. 2000. 19(3)-1. P. 352–358.
5. H a a k E., K v i k l y s D., L e p s i s J. Comparison of Cydonia and Pyrus
rootstocks in Estonia, Latvia and Lithuania // Sodininkystë ir darþininkystë. 2006. 25(3).
P. 322-326.
6. K v i k l i e n ë N., K v i k l y s D. Rootstock effect on maturity and quality
of ‘Auksis’ apples // Sodininkystë ir darþininkystë. 2006. 25(3). P. 258-263.
7. K v i k l i e n ë N., K v i k l y s D. Effect of vegetative, seedling and interstock
rootstocks on apple fruit maturity and storage // Growth and development of plants.
Theoretical and practical problems: abstracts of international scientific conference (Babtai,
7–9 June, 2004). 2004. Babtai. 52 p.
8. K v i k l i e n ë N., K v i k l y s D. Obelø vegetatyviniø poskiepiø átaka
‘Jonagold’ ir ‘Melrose’ vaisiø sunokimui ir kokybei // Sodininkystë ir darþininkystë. 2001.
20(1). P. 25–34.
9. K v i k l y s A. Obelø vegetatyviniø poskiepiø ávertinimas sode. Iðtvermingumas
þiemà ir auglumas // Sodininkystë ir darþininkystë. 1992. 11. P. 3–14.
10. K v i k l y s A. Þemaûgiai vaismedþiai. Vilnius: Mokslas, 1977. 128 p.
11. Kviklys A., Armolaitis E., Ðvirinas S. Intensyvus obelø sodas. Vilnius: Mokslas,
1988. 237 p.
12. K v i k l y s D. Þemaûgiø intarpø tyrimai obelø sode // Sodininkystë ir
darþininkystë. 1997. 16. P. 16–21.
13. K v i k l y s D., K v i k l i e n ë N., B i t e A., L e p s i s J., L u k u t
T., H a a k E. Baltic fruit rootstock studies: evaluation of 12 rootstocks for apple cultivar
‘Auksis’ // Sodininkystë ir darþininkystë. 2006. 25(3). P. 334-341.
14. K v i k l y s D., N. K v i k l i e n ë. Vegetatyviniø ir sëkliniø poskiepiø átaka
kriauðiø vaisiø kokybei // Sodininkystë ir darþininkystë. 2005a. 24(2). P. 11–19.
15. K v i k l y s D., K v i k l i e n ë N. Akiavimo aukðèio átaka obelø su B.396 ir
P 60 poskiepiais morfogenezei ir produktyvumui // Sodininkystë ir darþininkystë:
ataskaitinës mokslinës konferencijos medþiaga. 2005b. Babtai, Nr. 18. P. 9–14.
10
16. K v i k l y s D., K v i k l i e n ë N. Pear rootstock effect on growth,
productivity and fruit internal quality // Acta Horticulturae. 2004. 658(1). P. 359–364.
17. K v i k l y s D., K v i k l i e n ë N. Effect of rootstock on apple quality and
storability // Folia Horticulture. 2002. 14/1. P. 227–233.
18. K v i k l y s D. Poskiepiø átaka Konferencinë kriauðiø vegetatyvinei ir
generatyvinei raidai // Sodininkystë ir darþininkystë. 2005. 24(2). P. 3–10.
19. K v i k l y s D. Apple rootstock effect on the quality of planting material //
Acta Horticulturae. 2004. 658 (2). P. 641–646.
20. K v i k l y s D. Apple rootstock research in Lithuania with aspect to fruit quality
and tree productivity // Sodininkystë ir darþininkystë. 2002. 21(3). P. 3–13.
21. K v i k l y s D., S t a n k i e n ë J. Sodinamosios medþiagos sveikatingumo
átaka obelø veislës Ðampion augimui ir derëjimui jauname sode // Sodininkystë ir
Darþininkystë. 2005. 24(4). P. 48–56.
22. K v i k l y s D., U s e l i s N., K v i k l i e n ë N. Rootstock effect on
‘Jonagold’ apple tree growth, yield and fruit quality // Apple rootstocks for intensive
orchards. Warszawa, 1999. P. 67–69.
23. K v i k l y s D., P e t r o n i s P., K v i k l i e n ë N. Þemaûgiø poskiepiø
átaka obelø derliui // Sodininkystë ir darþininkystë. 2000. 19(1). P. 23–32.
24. R a þ a n s k i e n ë A., S t a n i e n ë G., R u g i e n i u s R.,
G e l v o n a u s k i e n ë D., Z a l u n s k a i t ë I., V e n s k i e n ë J., S t a n y s
V. Transformation of quince (Cydonia oblonga) with the rolB gene-based constructs
under different promoters // Journal of Fruit and Ornamental Plant Research. 2006. Vol.
14(1). P. 95–102.
25. Ð u m s k i s A. Obelø sëkliniø poskiepiø auginimas polietileniniuose
ðiltnamiuose // Sodininkystë ir darþininkystë. 1986a. 4. P. 21–27.
26. Ð u m s k i s A. Dirvos ruoðimas obelø poskiepiams pakartotinai auginti
polietileniniuose ðiltnamiuose // Sodininkystë ir darþininkystë. 1986b. 4. P. 29–35.
27. Ð v i r i n a s S. Sëkliniai obelø poskiepiai. Agropramoninis komitetas. Vilnius,
1986. 46 p.
28. U s e l i s N. Obelø su þemaûgiu poskiepiu biologiniø-ûkiniø savybiø tyrimas //
Sodininkystë ir darþininkystë. 2005. 24(4). P. 22–32.
29. U s e l i s N. Sodo konstrukcijø átaka Alva obelø su P 22 poskiepiu derliui,
produktyvumui bei vaisiø kokybei // Sodininkystë ir darþininkystë: ataskaitinës mokslinës
konferencijos medþiaga. Babtai, 2004. Nr. 17. P. 24–27.
30. U s e l i s N. Þemaûgiø obelø augumas ir produktyvumas ávairiø konstrukcijø
deranèiuose soduose // Sodininkystë ir darþininkystë. 2003. 22(1). P. 3–13.
31. U s e l i s N. Assessment of productivity and fruit quality of apple cultivars on
rootstock M26 in full bearing orchard // Sodininkystë ir darþininkystë. 2002. 21(3).
P. 14–28.
32. W e r t h e i m S. J. Rootstock guide: Apple, pear, cherry, European plum.
1998. Fruit Research Station, Wilhelminadorp, The Netherlands.
11
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 3–12.
OBELØ IR KRIAUÐIØ POSKIEPIØ TYRIMAI LIETUVOJE
D. Kviklys
Santrauka
Straipsnyje analizuojami ðiuo metu Lietuvos sodininkystës ir darþininkystës institute
atliekami obelø ir kriauðiø tyrimai. Tiriant obelø poskiepius, nustatoma poskiepiø ir aplinkos
sàlygø (geografiniø vietoviø) sàveika (Baltijos poskiepiø studija, kurià atlieka Baltarusijos,
Estijos, Latvijos, Lenkijos ir Lietuvos mokslo ástaigos), poskiepio reakcija á akiavimo aukðtá,
átaka vaisiø kokybei, sunokimo laikui ir laikymuisi, obelø su skirtingais poskiepiais formavimo
sistemos, poskiepiø naudojimas tarpiniam skiepijimui, poskiepiø sveikumas (tyrimai
atliekami su Nyderlandø mokslininkais), reakcija á gentiná dirvos nualinimà medelyne,
atsparumas ðaknø kaklelio puviniui, sausrai, átaka vaismedþiø fiziologiniams rodikliams,
sausøjø medþiagø pasiskirstymui ir maisto medþiagø pasisavinimui, atliekami paprastojo
svarainio poskiepiø genø inþinerijos tyrimai. Atliekant ávairius bandymus, tiriami ðie obelø
poskiepiai: M ir MM serijos – M.9, M.26, MM.106; P serijos – P 2, P 22, P 14, P 59, P 60,
P 61, P 62, P 66, P 67; B serijos – B.9, B.118, B.136, B.396, B.491, kiti poskiepiai – PB.4,
Bulboga, York 9, Pure 1 ir 'Paprastojo antaninio' sëjinukai, ir kriauðiø poskiepiai: Paprastojo
svarainio – QA, QC, Sydo, BA-29, S 1, K.11, K.16, K.19, 1.2, kriauðiø – Pyrodwarf, OHF333,
sëkliniai – Mostbirne ir Kazrausu. Lietuvos sodininkystës ir darþininkystës institute
poskiepiø tyrimus ávairiu lygiu atlieka 14 Sodø technologijø skyriaus, Genetikos ir
biotechnologijos skyriaus, Augalø apsaugos, Augalø fiziologijos bei Biochemijos ir
technologijos laboratorijø mokslo darbuotojø.
Reikðminiai þodþiai: Cydonia x oblonga, Malus x domestica, moksliniai tyrimai,
Pyrus x communis, poskiepis.
12
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 13–26.
EVALUATION OF PYRUS AND QUINCE ROOTSTOCKS
FOR HIGH DENSITY PEAR ORCHARDS
Frank MAAS
Applied Plant Research, Research Unit Fruit, Lingewal 1, 6668 LA
Randwijk, The Netherlands. E-mail: [email protected]
High density planting systems are a prerequisite to economise the use of land and
labour costs of orchards. Dwarfing rootstocks controlling the vigour of the scion cultivars
form the basis for such orchards.
In the Netherlands there are no breeding programs for fruit tree rootstocks. Rootstock
research is limited to and focussed on testing rootstocks selected in other countries. For
the Dutch pear growers the main selection criteria for new rootstocks are: 1) control of tree
size; 2) production; 3) fruit size; 4) fruit quality; 5) production efficiency; 6) frost resistance.
Additional criteria for Dutch fruit tree nurseries exporting trees to other countries are:
1) compatibility with scion cultivars; 2) suitability for growth in calcareous soils; 3) easy
propagation. In all trials rootstock performance is compared to quince MC, the most
commonly used rootstocks for pears in the Netherlands.
Recently, a number of pear (Pyrus communis) and quince (Cydonia oblonga)
rootstocks have been tested with ‘Conference’ and ‘Doyenné du Comice’ as the scion
cultivars.
Generally, the production efficiency of the Pyrus rootstocks was much less than for
quince MC. Another disadvantage of the evaluated Pyrus rootstocks was their high
sensitivity towards pear decline. Several rootstocks were rejected after examination of the
graft union because of suspected compatibility problems. Of the tested quince rootstocks
C 132 shows promise because of its control of tree growth in combination with good fruit
size and Eline® because of its reduction of fruit russeting in ‘Conference’.
Key words: Cydonia oblonga, graft compatibility, high density orchard, Pyrus
communis.
Introduction. High density planting systems are the starting point of modern
orchards. Small trees that come into production in the second year after planting are
a prerequisite to achieve regular yields of high quality fruits and to economise the use
of land and labour costs for pruning and picking. Dwarfing rootstocks controlling
the vigour of the scion cultivars and inducing precociousness form the basis for
such high density orchards (Wertheim and Webster, 2005).
European pears are predominantly grown on rootstocks of Quince (Cydonia
oblonga). In the Netherlands the majority of pears are grown on quince MC, but
13
quince MA and quince Adams are also used. ‘Conference’ is the most important
cultivar. Grown in high density planting systems yearly yields of 60 to 70 tons/ha are
feasible.
To obtain this production level a good control of shoot growth, flower bud
development, and fruit set is required. Although quince MC has been used successfully
for many decades in the Netherlands, there are several reasons to look for alternative
rootstocks.
Until 2001, the growth retardant chlormequat (CCC) was amply used the reduce
shoot growth and stimulate flower bud development. The loss of CCC has renewed
the interest in rootstocks more dwarfing than quince MC. Besides dwarfing of the
scion cultivar other desired traits of new rootstocks for pears are: 1) precociousness,
to ensure early productions starting in the second year after planting; 2) fruit size,
for ‘Conference’ pears the proportion of pears with a diameter >65 mm should be as
large as possible; 3) disease resistance, especially towards fire blight and pear decline;
4) compatible with scion cultivars; 5) frost resistance; 6) easy propagation;
7) suitability for growth on calcareous soils (absence of lime-induced chlorosis). In
addition, new rootstocks may also be used to meet the changes in market demands
for ‘Conference’ pears like larger and less russeted fruits.
Since there is no breeding program for pear rootstocks in the Netherlands, the
research on pear rootstocks is limited to testing rootstocks selected in other countries.
The main selection criteria for the Dutch pear industry are: 1) tree size; 2) production;
3) production efficiency; 4) fruit size distribution. Additional criteria for nurseries
exporting fruit trees to other countries are: 1) compatibility with as many modern
scion cultivars as possible; 2) suitability for growth in different soils; 3) easy
propagation.
During the past decades a large number of rootstocks were collected by Wertheim
(1998). The results of evaluation trials with several of these rootstocks have already
been published (Wertheim, 2002; Wertheim, Vercammen, 2000). This paper contains
the results of three more recent trials with the cultivars ‘Conference’ and ‘Doyenné
du Comice’ grafted on a number of other Quince and Pyrus rootstocks.
Materials and methods. P l a n t m a t e r i a l. All trials were planted in
the experimental orchard of the fruit research station at Randwijk (5.707° East,
51.937° North) in fresh soil consisting of river clay with 30% silt. Trees were planted
at a distance of 3.5 x 1.5 m and were trained as spindle trees according to local
commercial practice. Growth of the trees was not regulated by chemical growth
regulators, root pruning or girdling of the trunks. No gibberellins were applied to
stimulate fruit set. Contrary to common practice the rootstocks were not protected
by a layer of compost during the winter in order to evaluate the frost resistance of
the different rootstocks.
During a period of at least 5 years the growth and production of the trees was
monitored by:
- Annual or biannual measurement of the girth of the trunk at 30 cm above the
graft union
- Annual shoot growth on a scale from 1 (no shoot growth) to 9 (very vigorous
growth)
14
- Annual flower intensity on a scale from 1 (no flowers) to 9 (very rich flowering)
- Annual fruit production (number of fruits and kg fruits per tree)
- Analysis of mineral content of leaves and fruits (once for each trial 3 to 5
years after planting)
- Fruit size distribution (at least once for each trial 4 to 5 years after planting)
- Calculation of production efficiency (number of fruits/cm² trunk cross sectional
area)
T r i a l 1. (c o d e 0 4 4 - R a 9 9 1 0 7). Trees were planted on April 8th,
1998. The statistical design of the trial was a split plot with the scion cultivar being
the whole plot and the rootstocks the sub plots. Plots were replicated 8 times and
contained one tree of each treatment. In this trial the growth of ‘Conference’ and
‘Doyenné du Comice’ budded at 10 or 25 cm height was compared for the quince
rootstocks MC, C132, and the Pyrus rootstock BP10030 (Trajkovski, Andersson,
1990). Rootstocks were obtained from Naktuinbouw (Netherlands Inspection Service
for Horticulture) (MC), HRI East Malling, UK (C132), Eliteplantstation Balsgård,
Sweden (BP10030) and Fleuren Nurseries, Netherlands (Eline®). MC, C132 and
BP10030 were virus free. The virus-status of Eline® was unknown.
T r i a l 2 (c o d e 0 4 4 - R a 0 0 1 0 5). Trees were planted on March
30th, 2000. The statistical design of the trial was a split plot with the scion cultivar
being the whole plot and the rootstocks the sub plots. Plots were replicated 10 times
and contained one tree of each treatment. The growth of ‘Conference’ and ‘Doyenné
du Comice’ grafted on quince MC was compared with trees grafted on quince Sobu
and the Pyrus species Delbuena, Dolacomi, Gieser Wildeman and Pyrodwarf. Plant
material of Delbuena, Dolocomi and Gieser Wildeman was considered to be virusfree as they were grown from seed. MC and Sobu were obtained as virus-free
material. The virus status of Pyrodwarf was unknown.
T r i a l 3 (c o d e 0 4 4 - R a 0 1 1 0 1). Trees were planted on March
13th, 2001. The statistical design of the trial was a split plot with the scion cultivar
being the whole plot and the rootstocks the sub plots. Each plot was replicated 6
times and consisted of 3 trees per treatment. In this trial the growth of ‘Conference’
and ‘Doyenné du Comice’ grafted on Quince MC was compared with trees grafted
on the Quinces Adams, S 3, MC Peters, MH (=QR 193-16), ME and the pyrus
Gieser Wildeman. The virus status of S 3 and MH was unknown, all other rootstocks
were assumed to be virus-free as they were obtained from virus-free stock plants or
grown from seed (Gieser Wildeman).
S t a t i s t i c a l a n a l y s i s. The data were analysed using the Genstat
statistical program (release 8.1). In trial 1, the results of the trials with ‘Conference’
and ‘Doyenné du Comice’ were analysed separately because of the difference in the
duration of the trials. If possible, the data of all other trials were analysed using the
analysis of variance for a split plot. In case of significant differences (p<0.05), LSD
values were calculated and used for comparing treatment means in pairs.
Results. T r i a l 1 (0 4 4 - R a 9 9 1 0 7). As no significant effect of
budding height was observed on growth and production the data of both budding
heights were taken together. Pyrus BP10030 gave the lowest shoot growth index
and the smallest increase in trunk circumference (Table 1). With ‘Conference’ the
15
growth was very weak. Quinces C.132 and Eline® gave comparable to slightly more
growth in both ‘Conference’ and ‘Doyenné du Comice’.
T a b l e 1. Average growth parameters of ‘Conference’ and ‘Doyenné
du Comice’
1
l e n t e l ë.
‘Conference’ ir ‘Doyenné du Comice’ veisliø augimo rodikliø
vidurkiai
Increase of trunk circumference
Kamieno apimties padidëjimas, cm
Growth index*
Augimo indeksas
Rootstock
Poskiepis
MC
BP10030
C.132
Eline®
F-test
LSD05/R05
‘Conference’
2001–2005
4.7
2.4
5.0
5.4
b
a
bc
c
‘Doy. du Comice’
2001–2004
5.9
4.2
6.2
6.0
b
a
b
b
‘Conference’
Spring 1999 –
autumn 2005
1999 m. pavasaris–
2005 m. ruduo
12.6
7.9
13.6
13.7
b
a
b
b
‘Doy.
du Comice’
Spring 1999 –
autumn 2004
1999 m. pavasaris–
2004 m. ruduo
14.7
12.0
15.9
16.4
p<0.001
p<0.001
p<0.001
p<0.001
0.6
0.6
1.6
1.8
b
a
bc
c
*on scale 1 (no growth) to 9 (very strong growth) / skalëje nuo 1 (jokio augimo) iki 9 (labai
intensyvus augimas)
The cumulative production of ‘Conference’ on BP10030 was only 45% of that
on quince MC (Table 2). On quince C.132 ‘Conference’ produced slightly less and
on quince Eline® slightly more than on quince MC, but these differences were not
statistically significant. From 2000 to 2005 ‘Conference’ produced the largest number
of fruits on quince MC and quince Eline®, about 20% less fruits on quince C.132 and
approx. 50% less on BP10030. Despite the low number of fruits, the average fruit
weight was lowest on BP10030. On the quince rootstocks the average fruit weight
was the highest for the rootstock with the lowest number of fruits. Production
efficiency (number of fruits per cm² TCSA) was highest on quince Eline®, but not
statistically different from that on quince MC.
Cumulative production and total number of fruits of ‘Doyenné du Comice’ was
similar for all 4 rootstocks, but with an average production of only 32 kg and 125
fruits per tree much lower than the 87 kg and 500 fruits per tree for ‘Conference’ on
the tested quince rootstocks (Table 3). Average fruit weight of ‘Doyenné du Comice’
was highest on C.132 and least on Eline®. Production efficiency was highest for
BP10030.
The fruits harvested in 2003, 2004 and 2005 were graded in size. Table 4 shows
that C.132 gave the highest percentages of fruit with a diameter >65 mm. However
due to the large variation between the observations of trees these differences were
not statistically different in this trial.
16
T a b l e 2. Cumulative production of ‘Conference’ in 2000–2005
2
l e n t e l ë. ‘Conference’ derëjimo rodikliai 2000–2005 m.
Rootstock
Yield, kg/tree
Poskiepis
Derlius, kg/vaism.
MC
BP10030
C.132
Eline®
F-test
LSD05/R05
87.0
39.7
81.4
92.3
b
a
b
b
Amount of
fruits, pcs/tree
Vaisiø kiekis,
vnt./vaism.
503
266
433
563
c
a
b
c
Fruit weight
g
Vaisiø masë,
193
176
212
186
b
a
c
ab
Production efficiency,
fruits/cm2 of TCSA*
Produktyvumas, vaisiai/cm2 KSP
19.0
17.4
15.5
20.5
p<0.001
p<0.001
p<0.001
p<0.05
12.2
68
12
3.0
bc
ab
a
c
*
Total number of fruits per tree in 2000–2005 per cm2 of trunk cross sectional area (TCSA) in
autumn of 2005 / Bendras vaisiø skaièius 2000–2005 m. vienam kamieno skerspjûvio ploto (KSP) cm2
2005 rudená
T a b l e 3. Cumulative production of ‘Doyenné du Comice’ in 2000–2005
3
l e n t e l ë. ‘Doyenné du Comice’ derëjimo rodikliai 2000–2005 m.
Rootstock
Yield, kg/tree
Poskiepis
Derlius, kg/vaism.
Amount of
fruits, pcs/tree
Fruit weight
Vaisiø masë, g
Vaisiø kiekis,
vnt./vaism.
MC
BP10030
C.132
Eline®
F-test
Produktyvumas, vaisiai/cm2 KSP
34.2
31.6
31.2
31.6
133
128
112
129
287
299
304
268
ns
ns
p<0.05
p<0.01
26
1.1
LSD05/R05
ab
b
b
a
Production efficiency,
fruits/cm2 of TCSA*
4.4
5.5
3.4
4.3
ab
b
a
a
*
Total number of fruits per tree in 2000–2005 per cm2 of trunk cross sectional area (TCSA) in
autumn of 2005 / Bendras vaisiø skaièius 2000–2005 m. vienam kamieno skerspjûvio ploto (KSP) cm2
2005 rudená
Leaf appearance of both ‘Conference’ and ‘Doyenné du Comice’ grafted onto
BP10030 was not as healthy as on any of the other rootstocks. Many leaves were
pale green to yellowish. Mineral analysis of the leaves during the summer of 2002
revealed lower contents of K, Mg and Ca in ‘Conference’ and Mg and Ca in ‘Doyenné
du Comice’ (Table 5).
Flowering of ‘Conference’ was quite regular and good over the years 2000 to
2005. Average flower intensity over this period was between 5.5 and 6.2. Flowering
of ‘Doyenné du Comice’ was less regular. Average flower intensity from 2000 to
2005 varied between 3.5 and 5.3, with the lowest observed in 2001 (1.0 to 3.4) and
the highest in 2005 (7.3 tot 7.8). In both cultivars rootstock BP 10030 resulted in the
highest flower intensities.
17
T a b l e 4. Fruit size of ‘Conference’, % of total fruit yield
4
l e n t e l ë. ‘Conference’ vaisiø dydis, % bendro vaisiø kiekio
2003
Rootstock
Poskiepis
2004
2005
>55 mm
>65 mm
>55 mm
>65 mm
>55 mm
>65 mm
MC
BP10030
C.132
Eline®
F-test
91 b
50 a
94 b
88 b
p<0.001
52 c
6a
54 c
42 c
p<0.001
89
92
93
ns
33
40
40
ns
89
94
86
ns
48
62
40
ns
LSD05/R05
16
17
T a b l e 5. Mineral analysis of leaves harvested on August 26th, 2002
5
l e n t e l ë. Mineraliniø elementø kiekis lapuose, nuskintuose 2002 m.
rugpjûèio 26 d.
Rootstock
N
P
K
Mg
Ca
Fe
Mn
Zn
B
Cu
-1
Poskiepis
mg kg of dry weight
%
mg kg-1 sausojoje medžiagoje
‘Conference’
MC
2.12
0.19
1.21
0.24
1.76
75.8
75.0
58.2
22.2
6.5
C132
2.14
0.23
1.55
0.18
1.74
77.2
56.8
56.8
24.8
7.0
BP10030
2.10
0.18
0.99
0.14
1.22
68.0
85.5
68.2
24.5
6.0
Eline
2.05
0.18
1.28
0.22
1.72
68.8
73.2
51.5
22.8
4.4
F-test
ns
ns
*
***
***
ns
*
ns
ns
ns
0.4
0.03
0.18
®
LSD05/R05
19.0
‘Doyenné du Comice’
MC
1.83
0.17
1.36
0.30
1.81
64.0
80.2
69.0
22.5
5.8
C132
1.89
0.17
1.46
0.22
1.59
72.2
65.8
62.8
24.5
4.7
BP10030
1.77
0.17
1.32
0.14
1.14
62.2
72.8
57.5
25.0
4.9
Eline
1.87
0.18
1.42
0.26
1.76
70.5
69.5
64.5
22.5
5.8
F-test
*
*
ns
***
***
*
∼
ns
∼
**
LSD05/R05
0.08
0.01
0.04
0.20
9.1
10.4
2.2
0.6
®
~ towards significant difference / artima esminiam skirtumui
At the end of the trial the graft unions of ‘Conference’ and ‘Doyenné du Comice’
grafted on BP10030 were examined. The bark was removed and longitudinal sections
were made of the graft unions. Figure 1 shows the longitudinal sections of the graft
unions of both scion cultivars grafted onto BP10030. As can be seen in this figure,
compatibility between BP10030 looks good and ‘Conference’ is very poor, while
that between Sobu and ‘Doyenné du Comice’ seems to be much better. However,
also in the latter combination a clear separation line between the wood of the scion
18
and the rootstock is visible indicating both tissues are also not fully compatible.
T r i a l 2 (0 4 4 - R a 0 0 1 0 5). Table 6 shows that with ‘Conference’
rootstock Sobu gave the weakest growth. Differences in growth between all other
combinations were quite small. With ‘Doyenné du Comice’ growth index and increase
in trunk diameter were similar for all rootstocks used in the trial.
T a b l e 6. Average growth parameters of ‘Conference’ and ‘Doyenné
du Comice’
6
l e n t e l ë.
Rootstock
Poskiepis
‘Conference’ ir ‘Doyenné du Comice’ augimo rodikliø vidurkiai
Growth index* in 2000–2004
Augimo indeksas 2000–2004 m.
‘Conference’
MC
Delbuena
Dolacomi
Gieser W.
Pyrodwarf
Sobu
F-test
3.6
4.3
5.1
5.6
5.7
2.5
p<0.001
LSD05/R05
1.1
ab
bc
c
c
c
a
‘Doy. du Comice’
5.0
6.2
5.0
6.1
5.5
4.9
n.s.
Increase of trunk circumference in
spring 2000–autumn 2005
Kamieno apimties padidëjimas 2000 m.
pavasará–2005 m. rudená, cm
‘Conference’
8.6
8.5
11.3
11.9
12.8
5.4
p<0.001
b
b
b
bc
c
a
‘Doy. du Comice’
11.6
13.5
13.0
12.7
14.3
11.9
n.s.
2.8
*on scale 1 (no growth) to 9 (very strong growth). n.s = not significant / skalëje nuo 1 (jokio
augimo) iki 9 (labai intensyvus augimas); n.s. = nereikðminga
Table 7 summarises the production of ‘Conference’ and ‘Doyenné du Comice’
grown on four different Pyrus cultivars and quince Sobu as a rootstocks in comparison
with the standard rootstock quince MC. Production was highest on quince MC and
did not differ significantly between the 4 Pyrus rootstocks and quince Sobu. Despite
the lower fruit numbers, average fruit weights on Dolacomi and Gieser Wildeman
were lower than on MC and Pyrodwarf.
With ‘Doyenné du Comice’ quince Sobu was second best with respect to
production and production efficiency.
‘Conference’ trees on Sobu did not look as healthy as on the other rootstocks
and growth of the cultivar was much weaker than that of ‘Doyenné du Comice’ on
the same rootstocks, indicating some kind of incompatibility between ‘Conference’
and Sobu. At the end of the trial a longitudinal sections were made of the graft unions
of both scion cultivars grafted onto Sobu. Figure 2 shows the longitudinal sections
of the graft unions between Sobu and both cultivars. As can be clearly seen in this
figure, part of the wood at the union is black, which indicates compatibility between
Sobu and ‘Conference’ is very poor. The union between Sobu and ‘Doyenné du
Comice’ looks much healthier. However, also in the latter combination a clear separation
line between the wood of the scion and the rootstock is visible, indicating that also in
this case both tissues are not fully compatible.
19
T a b l e 7. Cumulative production of ‘Conference’ and ‘Doyenné du
Comice’, 2001–2004
7
l e n t e l ë. ‘Conference’ ir ‘Doyenné du Comice’ derëjimas 2001–2004 m.
Rootstock
Poskiepis
Yield, kg/tree
Derlius,
kg/vaism.
Amount of
fruits, pcs/tree
Vaisiø kiekis,
vnt./vaism.
Fruit weight
Vaisiø masë, g
Production efficiency,
fruits/cm2 of TCSA*
Produktyvumas, vaisiai/cm2 KSP
‘Conference’
MC
28.9
172
190
10.2 e
Delbuena
16.4
114
160
6.4 d
Dolacomi
17.3
118
153
4.6 bc
Gieser W.
18.6
138
139
5.3 cd
Pyrodwarf
17.3
123
175
Sobu
16.3
109
151
MC
24.3
98
263
4.1 bc
Delbuena
11.5
44
270
1.4 a
Dolacomi
8.1
36
232
1.1 a
Gieser W.
9.5
33
259
1.2 a
Pyrodwarf
8.6
30
263
0.9 a
17.0
69
243
3.2 b
4.3 bc
10.6 e
‘Doyenné du comice’
Sobu
Average of ‘Conference’ & ‘Doyenné du comice’ / ‘Conference’ ir ‘Doyenné du comice’ vidurkis
MC
26.6 b
135 b
227 b
Delbuena
13.8 a
80 a
212 ab
Dolacomi
12.6 a
77 a
194 a
Gieser W.
13.8 a
85 a
197 a
Pyrodwarf
13.1 a
77 a
224 b
Sobu
F-test
LSD05/R05
17.4 a
91 a
204 ab
p<0.001
p<0.001
p<0.05
p<0.01
5.6
31
25
1.5
*
Total number of fruits per tree in 2001-2004 per cm2 of trunk cross sectional area (TCSA) in
autumn of 2004 / Bendras vaisiø skaièius 2001–2004 m. vienam kamieno skerspjûvio ploto (KSP) cm2
2004 rudená
20
F i g. 1. Longitudinal sections of graft unions of 8-year old trees of ‘Conference’ (A)
and ‘Doyenné du Comice’ (B) grafted on rootstock BP10030
1
p a v. Aðtuonmeèiø ‘Conference’ (A) ir ‘Doyenné du Comice’ (B) veisliø vaismedþiø
su BP10030 poskiepiu iðilginis skiepijimo vietos pjûvis
F i g. 2. Longitudinal sections of graft unions of 8-year old trees Conference (A) and
Doyenné du Comice (B) grafted on rootstock Sobu
2
p a v. Aðtuonmeèiø ‘Conference’ (A) ir ‘Doyenné du Comice’ (B) veisliø vaismedþiø
su Sobu poskiepiu iðilginis skiepijimo vietos pjûvis
Average flower intensities over the trial period were between 4.4 and 5.4 for
‘Conference’ and 3.4 and 4.9 for ‘Doyenné du Comice’ . In both cultivars the lowest
flower intensities were noted for trees grown on Gieser Wildeman and the highest
for trees grown on quince MC.
T r i a l 3 (0 4 4 - R a 0 1 1 0 1). In Table 8 the growth and production of
‘Conference’ and ‘Doyenné du Comice’ on quince MC is presented together with
that on 5 other quinces (Adams, MC Peters, MH (= QR 193-16), ME, and S 3) and
on the pyrus Gieser Wildeman. Both scion cultivars showed similar patterns in growth.
21
Compared to growth on quince MC a significantly higher growth index and a larger
increase in trunk circumference was noted on both Gieser Wildeman and S 3. On
MC Peters the growth index and increase in trunk circumference equalled those on
MC. On Adams growth index of ‘Conference’ equalled that on MC, while that of
‘Doyenné du Comice’ was slightly higher. No differences were observed in the
increases in trunk circumferences of both scion cultivars on MC and Adams. With
the exception of a smaller increase in trunk circumference of ‘Doyenné du Comice’,
growth of both scion cultivars on MC Peters equalled that on MC. Significantly
lower growth indexes were observed in both scion cultivars on quinces MH and ME.
Increases in trunk circumferences were also smaller on these rootstocks, but these
differences were only statistically significant in ‘Doyenné du Comice’ .
T a b l e 8. Average growth index and increase in trunk
circumference
8
l e n t e l ë.
Rootstock
Poskiepis
MC
Adams
S3
Gieser W.
MC Peters
MH
ME
F-test
LSD05/R05
Vidutinis augimo indeksas ir kamieno apimties padidëjimas
Growth index* in 2002–2005
Augimo indeksas 2002–2005 m.
‘Conference’
4.6 cde
5.0 def
6.0 g
5.5 fg
4.4 bcd
3.8 ab
3.2 a
p<0.001
0.6
Increase of trunk circumference in
spring 2001–autumn 2005
Kamieno apimties padidëjimas 2001 m.
pavasará–2005 m. rudená, cm
‘Doy. du Comice’
‘Conference’
4.3 bcd
8.2 ab
5.1 ef
9.0 b
5.9 g
12.1 d
6.8 h
10.3 c
4.3 bc
8.1 ab
3.4 a
7.7 a
2.9 a
7.5 a
p<0.001
p<0.001
0.6
1.2
‘Doy. du Comice’
10.4 c
10.9 c
14.0 e
14.8 e
9.0 b
7.9 ab
7.8 ab
p<0.001
1.2
*on scale 1 (no growth) to 9 (very strong growth) / skalëje nuo 1 (jokio augimo) iki 9 (labai
intensyvus augimas)
The average growth on Gieser Wildeman presented in Table 7 was somewhat
reduced by the occurrence of pear decline in some years in several observation
trees. In any year trees on Gieser Wildeman without any visual symptoms of pear
decline showed a much stronger growth than on MC.
Contrary to an earlier experiment at the former location of the research station
in Wilhelminadorp (Wertheim, 2002), growth on S 3 was stronger than on MC. The
most probable explanation for the weaker growth in Wilheminadorp was the use of
virus-infected S 3. The growth on virus-free S 3 in the experiment in Randwijk
indicates that this rootstock is too vigorous for Dutch high density orchards.
Cumulative productions of ‘Conference’ and ‘Doyenné du Comice’ are shown
in Table 9. ‘Conference’ produced the highest number of fruits on the MC, Adams
and MC Peters. On S 3, Gieser Wildeman and MH trees produced about 100 fruits
less. On ME trees produced only one third of the number of fruits as compared to
trees on MC. ‘Conference’ trees produced similar kg fruits on MC, Adams and MC
22
Peters. On S 3 and MH trees produced about 15 kg less. Trees on Gieser Wildeman
and ME produced about 26 and 34 kg less, respectively, than on MC. Average fruit
weight was only significantly reduced for ‘Conference’ grown on Gieser Wildeman.
Production efficiency was highest for ‘Conference’ on MC. Trees on Adams and
MC Peters had slightly lower production efficiency, but the difference to MC was
not statistically significant. Significant lower efficiencies compared to MC were noted
for ‘Conference’ on MH (-17%), ME (-46%), and S 3 (-52%) and Gieser Wildeman
(-54%).
T a b l e 9. Production parameters of ‘Conference’ and ‘Doyenné du
Comice’, 2002–2005
9
l e n t e l ë. ‘Conference’ ir ‘Doyenné du Comice’ derëjimo rodikliai 2002–2005 m.
Rootstock
Yield, kg/tree
Poskiepis
Derlius, kg/vaism.
Amount of fruits,
pcs/tree
Vaisiø kiekis,
vnt./vaism.
Fruit weight
Vaisiø masë, g
Production efficiency,
fruits/cm2 of TCSA*
Produktyvumas, vaisiai/cm2 KSP
‘Conference’
MC
329 h
54.8 g
177 b
18.9 f
Adams
327 h
55.5 g
176 b
17.0 ef
S3
211 g
38.4 ef
190 b
9.0 d
Gieser W.
215 g
27.1 c
134 a
8.6 d
MC Peters
293 h
52.0 g
188 b
16.9 ef
MH
222 g
40.0 ef
188 b
15.8 e
ME
109 def
19.6 b
187 b
10.3 d
MC
90 cde
‘Doyenné du comice’
28.4 cd
4.8 bc
5.6 c
38.0 ef
294 d
S3
79 cd
24.9 bc
317 def
2.9 b
Gieser W.
25 a
6.1 a
247 c
0.7 a
MC Peters
119 ef
35.0 de
301 de
6.2 c
19.9 b
330 f
4.7 bc
Adams
135 f
324 ef
66 bc
MH
37 ab
ME
F-test
LSD05/R05
P<0.001
40
12.4 a
362 g
P<0.05
P<0.05
7.0
26
3.3 b
P<0.001
2.1
Total number of fruits per tree in 2002–2005 per cm2 of trunk cross sectional area (TCSA) in
autumn of 2005 / Bendras vaisiø skaièius 2002–2005 m. vienam kamieno skerspjûvio ploto (KSP) cm2
2005 rudená
*
Compared to ‘Conference’ fruit production of ‘Doyenné du Comice’ was lower
for all rootstock. The highest number of fruits and kg/tree were produced on Adams,
MC Peters and MC, the lowest numbers on Gieser Wildeman and ME. Average fruit
size was highest on ME and lowest on Gieser Wildeman. Production efficiency was
highest on MC Peters followed by Adams, MC and MH. Gieser Wildeman gave by
far the lowest production efficiency.
23
Flower intensity over the trial period was generally good and averaged between
4.9 and 6.4 in ‘Conference’ and 3.6 and 6.0 in ‘Doyenné du Comice’ . In both
cultivars the lowest flower intensities were observed for trees grown on pyrus Gieser
Wildeman or quince ME, the highest flower intensities for trees grown on the quinces
MC, Adams and MC Peters.
Discussion. ‘Conference’ and ‘Doyenné du Comice’ trees raised from the same
batch of rootstocks and scion buds and at the same nursery in the Netherlands were
also planted in 1999 in a trial at East Malling Research in England (Johnson et al.,
2005). Compared to the Dutch trial production of ‘Conference’ in the UK was lower
and the percentage of fruits having a diameter of 65 mm or more was much lower
for trees grown on rootstocks MC and C132. With ‘Conference’ the Pyrus rootstock
BIP10030 was less productive. In the trial in England this was not yet noticeable in
2003 (Johnson et al., 2005), but became very clear in 2004 (Johnson, personal
communication, 2006). The observed tendency of C132 increasing fruit size of
‘Conference’ in the Dutch trial confirmed by the results of the trial in England. The
negative effect of leaf appearance of ‘Conference’ grafted on BP10030 together
with the decreased productivity warrants further attention and may possibly be the
result of a cultivar – specific incompatibility. Although such negative effects were
not observed with cultivar ‘Doyenné du Comice’, the formation of a very thickened
graft union may possibly affect graft compatibility in the future and thus necessitates
further research.
An interesting observation was the reduction of russeting of ‘Conference’ when
grown on rootstock Eline®. This may be of interest when the market demands fruits
with less russeting, which may be of interest for market demanding less russeted
pears.
Frost resistance is expected to be another advantage of both Eline® and C132 as
they were originate from areas with much more severe winters. However, lack of
severe winter frosts during the trial period made it not possible to evaluate this
characteristic.
Pyrus rootstocks are attractive from the point of view of better compatibility,
frost hardiness and tolerance to lime-induced chlorosis than most quince rootstocks.
However, all Pyrus rootstocks evaluated so far resulted in stronger growth, a lower
production efficiency and general smaller fruit size than quince MC. In addition,
another negative aspect of Pyrus rootstocks is their observed sensitivity to pear
decline. Of the tested quinces the weakest growth and highest production efficiency
was observed for ‘Conference’ and ‘Doyenné du Comice’ grown on Sobu. However,
based on the anatomy of the graft union and the poor leaf quality the dwarfing by
this rootstock seems to be caused by incompatibility, especially with ‘Conference’.
Large variation was observed in vigour between the 10 replicate trees of the trial,
indicating variability in the establishment of a successful graft union. As virus free
plant material of Sobu was used, it is unlikely that viruses were the reason for the
differences in growth between the trees. Quinces MH, Eline®, and C132 were the
best performing rootstocks of the trials and their control of tree vigour and production
efficiency was quite similar to quince MC. Specific characteristics like slightly more
dwarfing (MH), bigger fruit size (C 132) and expected greater frost resistance
24
(C 132, Eline®), less russeted fruits with ‘Conference’ (Eline®) may favour their
choice above the currently most used quince rootstocks MC and Adams, depending
on the desired planting system, scion cultivar and market demands for fruit size and
russeting. A larger demonstration trial is in preparation to compare this growth and
production of ‘Conference’ with these three rootstocks in comparison with MC and
Adams at different locations in the Netherlands and to further optimise cultivation
practises.
Gauta
2006 05 05
Parengta spausdinti
2006 08 03
References
1. J o h n s o n D., E v a n s K., S p e n c e r J., W e b s t e r T., A d a m
S. Orchard Comparisons of New Quince and Pyrus Rootstock Clones. Acta Hort. 2005.
671: 201–207.
2. T r a j k o v s k i V., A n d e r s s o n G. Rootstock Breeding. 1990. Sveriges
Lantbrukuniversitet. Balsgård – Avdelningen För Hortikulturell Växtförädling.
Verksamhetsberättelse 1988–1989: 27–30.
3. W e r t h e i m S. J. Rootstock guide. Apple, pear, cherry, European plum.
Publication Fruit Research Station, Wilheminadorp, 1998. P.144.
4. W e r t h e i m S. J., W e b s t e r A. D. Rootstocks and interstems. In: Tromp
J., Webster A.D., Wertheim S.J. (eds). Fundamentals of Temperate Zone Tree Fruit
Production. Backhuys Publishers, Leiden, 2005. P. 156–175.
5. W e r t h e i m S. J. Rootstocks for European pear: a review. Acta Hort. 2002.
596: 299–309.
6. W e r t h e i m S. J., V e r c a m m e n J. A multi-site pear-interstem trial in the
Netherlands and Belgium. J. Amer. Pomol. Soc. 2000. 54: 199–207.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 13–26.
KRIAUÐIØ IR SVARAINIØ POSKIEPIØ TINKAMUMAS INTENSYVIEMS
KRIAUÐIØ SODAMS
F. Maas
Santrauka
Siekiant ekonomiðkai iðnaudoti þemæ ir taupyti darbo sànaudas soduose, bûtina
taikyti tankaus sodinimo sistemas. Tokiø sodø pagrindas yra þemaûgiai poskiepiai,
kontroliuojantys vaismedþiø augimà.
Olandijoje nëra vaismedþiø poskiepiø selekcijos programø. Poskiepiø tyrimai – tik
kitose ðalyse sukurtø poskiepiø patikrinimas. Olandijos kriauðiø augintojams pagrindiniai
naujø poskiepiø selekcijos kriterijai yra ðie: 1) vaismedþio dydþio kontrolë; 2) produkcija;
3) vaisiø dydis; 4) vaisiø kokybë; 5) produktyvumas; 6) atsparumas ðalèiams. Papildomi
25
kriterijai Olandijos medelynams, eksportuojantiems vaismedþius á kitas ðalis, yra ðie:
1) poskiepiø suderinamumas su skiepijamomis veislëmis; 2) tinkamumas auginti
kalkinguose dirvoþemiuose; 3) nesudëtingas dauginimas. Visuose bandymuose poskiepiø
charakteristikos lyginamos su svarainiu MC, Olandijoje kriauðëms daþniausiai naudojamu
poskiepiu.
Neseniai keletas kriauðiø (Pyrus communis) ir svarainiø (Cydonia oblonga) poskiepiø
buvo patikrinti su ‘Conference’ ir ‘Doyenné du Comice’ veislëmis.
Paprastai kriauðiø poskiepiø produktyvumas yra daug maþesnis negu svarainiø MC.
Kitas ávertintø kriauðiø poskiepiø trûkumas buvo jø didelis jautrumas kriauðiø nykimo
fitoplazmai. Patikrinus skiepijimo vietà, keletas poskiepiø buvo atmesta dël átariamø
suderinamumo problemø. Ið patikrintøjø svarainiø poskiepiø daug vilèiø teikia C132 (riboja
vaismedþiø augimà ir uþtikrina gerà vaisiø dydá) ir Eline® (sumaþina ‘Conference’ veislës
kriauðiø vaisiø grûdëtumà).
Reikðminiai þodþiai: Cydonia oblonga, intensyvus sodas, Pyrus communis,
suderinamumas.
26
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 27–33.
ROOTSTOCKS USED FOR TEMPERATE FRUIT TREES
IN TURKEY: AN OVERVIEW
Sezai ERCISLI, Ahmet ESITKEN, Emine ORHAN,
Ozlem OZDEMIR
Ataturk University, Agricultural Faculty Department of Horticulture, 25240
Erzurum-Turkey. E-mail: [email protected]
Most of the fruit tree orchards in Turkey are grafted onto rootstocks, except chestnuts
and cornelian cherries, which are generally propagated by seeds. The main rootstocks
used by Turkish growers for temperate fruit trees nowadays are: wild apple seedlings, M.9
and MM.106 for apples; wild pear, in particular Pyrus eleagrifolia L. seedlings for pears;
wild peach seedlings for peaches; wild plum seedlings for plums; seedlings of Mazzard
and Mahaleb, very recently clonally propagated Gisela 5 and Gisela 6 rootstocks for
cherries; Juglans regia L. seedlings for walnut; wild almond seedlings for almond; wild
apricot seedlings for apricot. The level of clonal rootstock use for temperate fruit tree
species is not satisfactory in Turkey. However, in recent years the number of orchards
established with clonal rootstocks, in particular for apples and cherries, has been increased
in the country. In this paper the current status of rootstock use for temperate fruit trees in
Turkey is reported.
Key words: temperate fruit trees, rootstock use, Turkey.
Introduction. Agriculture traditionally has been a pillar of Turkey’s economy.
Although the industrial and service sectors increased their dominance in
recent years, Turkey remained the largest producer and exporter of agricultural
products in the Middle East and North African region. Turkey’s fertile soil and hardworking farmers make the country one of the few in the world that is self-sufficient
in terms of food. The total land area of Turkey is about 78.3 million ha supporting
26.4 million ha of agricultural and 20.7 million ha of forest land (Ayyildiz et al., 1997;
Anonymous, 2005).
Turkey’s natural environment is very diverse, ranging from subtropical to cold
temperate. This ecological diversity has contributed not only to a high genetic diversity,
but has also allowed the successful introduction and cultivation of a great number of
fruit tree species. Thus, over 85 fruit tree species including almost all the deciduous
species such as apples, pears, cherries, quinces, almonds, pistachios etc. are grown
successfully in the country (Ercisli, 2004).
The country dominates in the world by hazelnut, apricot, sweet cherry, fig and
quince production (FAO, 2005). Fruit production is conducted throughout the
country, although it is less common in the mountainous Eastern regions, where
27
animal husbandry is the principal activity.
The development of the Turkey’s fruit industry has been remarkable in the last
decade. Currently planted fruit tree area is more than 240.000 ha, mainly central area
of the country. Previously, Turkey’s fruit industry was based mainly on dried fruit
export, but recently fresh fruit export gained importance. Hazelnut, sweet cherry,
citrus, fig and dried apricot export have an important place in Turkish economy
(FAO, 2005). One of the important factors, which affect this improvement in Turkey,
is the use of rootstocks for different fruit tree species.
As well known, the use of rootstocks is very important in fruit tree growing not
only for yield efficiency, mineral uptake, hardiness etc., but also to meet specific
cultural needs, aside from vigor management, with adaptability to climatic and edaphic
conditions having a high priority requirement (Ercisli et al., 2000).
During the last two decades, the use of clonal rootstocks for temperate fruit
tree crops such as apples, cherries, and nectarines, particularly increased in Turkey.
The aim of this study was to give latest information on the use of rootstocks in
Turkey for temperate fruit tree crops.
Materials and methods. The data used in this study was obtained from Ministry
of Agriculture of Turkey (www.tarim.gov.tr).
Results. Stone Fruit Rootstocks. The seedling and clonal rootstocks, their
percentage and number of rootstocks produced in Turkey in 2005 for stone fruits
are listed in Table 1.
It can be seen in Table 1 that the great majority of rootstocks used for apricot
cultivars in Turkey were still wild apricot seedlings (95.99%). Apricot culture was
practiced in Turkey more than 1000 years ago and the use of plantations of
systematically grafted trees was started from 1960’s. In some parts of Turkey, for
example, in Erzincan plain, the majority of apricot trees come from ungrafted seedling
material. However, in modern orchards of Turkey, the cultivars are grafted in general
on wild apricot seedling rootstocks using T-budding method. The use of other Prunus
species such as Prunus cerasifera, Prunus persica and Prunus
armeniaca L. seedlings is restricted by problems of graft incompatibility (Unal, 1992).
According to the latest data, Turkey occupy 1st place both by sweet cherry
production and export levels in the world (FAO, 2005). Primary sweet cherry
rootstocks used in Turkey are wild Prunus avium L. (Mazzard) seedlings (40.12%)
and followed by Prunus mahaleb L. seedlings (28.75%), Gisela 6 (Prunus cerasus x
Prunus canescens) (14.84%) and Gisela 5 (Prunus canescens x Prunus cerasus)
(10.01%) rootstocks, respectively (Table 1). Turkish growers mainly prefer to use
Mazzard seedlings for sweet cherries because of its good soil adaptability. In general,
Prunus mahaleb L. seedlings were used for sweet cherries only on calcareous droughty
soils in Turkey. In latest years the use of Gisela 5 and Gisela 6 rootstocks has been
widespread very quickly. On the other hand, Prunus mahaleb L. seedlings (92.22%)
still remain the main choice for Turkish sour cherry producers because of its high
compatibility with sour cherry cultivars, tolerance to drought, smaller tree size, good
precocity, and high productivity. In Turkey, the trees of Prunus mahaleb L. with
yellow fruited and light-colored trunks are generally preferred for rootstock for both
sweet and sour cherry cultivars. It is believed that these types do not show
incompatibility with scion cultivars (Misirli et al., 1996).
28
T a b l e 1. Stone fruit rootstocks propagated, percentage and quantity
of grafted plants produced in Turkey nurseries in 2005
1
l e n t e l ë. Kaulavaisiø poskiepiai, Turkijos medelynuose 2005 metais áskiepytø
augalø procentas ir kiekis
Fruit tree crops
Rootstocks
Augalo rûðis
Poskiepiai
Apricots / Abrikosai
Sweet cherries
Treðnës
Sour cherries
Number of grafted
plants
Áskiepytø augalø skaièius
%
units/vnt.
Nemaguard
3.70
30 000
Wild plum seedlings / Laukiniø slyvø sëjinukai
0.31
2550
Wild apricot seedlings / Laukiniø abrikosø sëjinukai
95.99
810 822
Mahaleb seedlings / Mahaleb sëjinukai
28.70
583 368
Mazzard seedlings / Mazzard sëjinukai
40.12
813 912
SL 64
6.33
128 400
Gisela 5
10.01
203 120
Gisela 6
14.84
301 000
Mahaleb seedlings / Mahaleb sëjinukai
92.22
296 163
Vyšnios
Peaches / Persikai
Wild sour cherry seedlings / Laukiniø vyšniø sëjinukai
6.53
20 985
Wild sweet cherry seedlings / Laukiniø trešniø sëjinukai
1.25
4 000
Nemaguard
1.24
10 000
Almond seedlings / Migdolø sëjinukai
0.20
2 000
GF 677
2.29
18 500
Marianna GF8-1
1.24
1 000
Wild peach seedlings / Laukiniø persikø sëjinukai
94.51
764 629
Wild apricot seedlings / Laukiniø abrikosø sëjinukai
0.50
4 315
GF 305
0.02
143
Nectarines/Nektarinai GF 677
59.96
35 500
Marianna GF8-1
16.89
10 000
Wild peach seedlings / Laukiniø persikø sëjinukai
6.26
3 705
Nemaguard
16.89
10 000
Marianna GF8-1
4.42
20 000
Wild plum seedlings / Laukiniø slyvø sëjinukai
80.78
367 768
Wild apricot seedlings / Laukiniø abrikosø sëjinukai
0.30
1 380
Myrobalan B
14.00
63 400
Plums / Slyvos
Almonds / Migdolai
GF 677
3.00
4 000
Wild almond seedlings / Laukiniø migdolø sëjinukai
97.00
115 343
29
Wild peach seedlings still are the principal rootstock source for peach cultivars
in Turkey with the percentage of use – 94.51% (Table 1). The wild peach types are
usually obtained from peach trees that have escaped cultivation and are found growing
wild or in a nearly wild state. A major problem with wild peaches is their genetic
variability and general lack of uniformity in the nursery and the orchard (Guleryuz,
1998).
In Turkey, most of plum trees are found in wild or semi-wild conditions. Plant
characteristics of plum species naturally grown in Turkey are very diverse, ranging
from shrubs to large trees, spreading to upright and early to late blooming (Ercisli,
2004). Wild seed propagated rootstocks (80.78%) mainly from Prunus cerasifera L.
species have been used. Turkish growers believe that less incompatibility is seen when
European plums are put on this species (Gonulsen et al., 1985). Myrobalan B is the
second widely used seedling rootstock in Turkey with sharing of 14% (Table 1).
Until 1980’s almond trees originally were grown ungrafted as seedlings in Turkey.
Now grafting, mainly onto almond seedlings (97%), is common way for almond
production in Turkey. Field budding practices onto seedlings in main almond growing
regions in Turkey is desirable because of deeper and longer tap-rooted characteristics
of seedlings. Field budded trees in these regions are considered to be more resistant
to dry conditions. On the other hand, seeds from bitter almond trees have been
characteristically used by nurserymen as sources of seeds. Trees from such sources
are thought to be more vigorous and generally superior to trees from sweet-kernelled
seeds. It is possible that such seeds are less often eaten by rodents and thus survive
better in field planting (Akca and Ceylan, 1996).
P o m e R o o t s t o c k s. The main rootstocks used for apple cultivars in
Turkey were wild apple seedlings (37.07%), M.9 (35.96%) and MM.106 (22.60%)
(Table 2).
The center of genetic diversity of apple (Malus) is in Asia Minor (Turkey),
likewise the cradle of human civilization. M. pumila L. and M. trilobata L. are native
Anatolia (Way et al., 1990). A large number of wild apple populations’ originated
from the Black Sea and Northeast regions of Turkey. These wild germplasm are
critical in maintaining diversity in the gene pool. A research project on genes controlling
economic traits of Malus species found in Turkey is being carried out by apple
breeders, plant pathologists and germplasm curators (McCandless, 1999). Though
the fruit quality of these wild species is very poor, the possible frost and drought
tolerance and dwarf growth habit might be valuable genetic traits for apple rootstocks
breeding. If these wild plants came true-to-type from seed, this could be a source of
apomixes for use in breeding rootstocks.
Throughout Turkey, the most common rootstock used for pear cultivars still is
wild pear seedlings, in particular Pyrus elaeagrifolia with 97.0% (Table 2). Pyrus
elaeagrifolia L. originated in Crimea, Anatolia, East Bulgaria, Romania, and European
Turkey. The species shows high drought and cold resistance and therefore provides
one of the most commonly used rootstocks for pear cultivars in Turkey (Guleryuz,
1998).
30
T a b l e 2. Pome rootstocks propagated, percentage and quantity of
grafted plants produced in Turkey nurseries in 2005
2
l e n t e l ë. Sëklavaisiø poskiepiai, Turkijos medelynuose 2005 metais áskiepytø
augalø procentas ir kiekis
Number of grafted plants
Fruit tree crops
Vaismedžiai
Rootstocks
Áskiepytø augalø skaièius
Poskiepiai
%
units / vnt.
Apples / Obelys
M.9
M.26
MM.106
MM.109
MM.111
Wild apple seedlings/ Laukiniø obelø sëjinukai
35.96
1.06
22.60
0.02
3.31
37.07
950 936
28 108
598 176
5670
87 915
984 118
Pears / Kriauðës
Quince A / Svarainis A
Wild quince seedlings / Laukiniø svarainiø sëjinukai
Wild pear seedlings / Laukiniø kriaušiø sëjinukai
2.99
0.01
97.0
13 512
210
488 037
Quinces / Svarainiai
Quince A / Svarainis A
Wild quince seedlings / Laukiniø svarainiø sëjinukai
19.0
81.0
21 790
90 475
N u t C r o p R o o t s t o c k s. Pistachios. In Turkey, there are wild
pistachio populations including Pistacia vera, Pistacia khinjuk and Pistacia terebinthus
trees or shrubs. These wild plants are being grafted in situ conditions by standard
pistachio cultivars. However, in modern pistachio orchards, pistachios are
commercially propagated by budding the chosen scion cultivar onto seedling
rootstocks (100 percent Pistacia vera L. seedlings used). Therefore, the rootstocks
for used pistachios cultivars in Turkey, however, are genetically variable, since the
seed from which it grew was the progeny of a heterozygous female parent and
unknown heterozygous pollen parent (Guleryuz, 1998).
Walnuts. In Turkey, both seedling and grafted walnut (Juglans regia L.) trees
are grown throughout the country. The cultivars mainly grafted onto wild walnut
seedlings (Juglans regia L.). Currently all seed propagated rootstocks in Turkey are
derived from open pollinated seeds. Breeding and selection programs in Turkey are
focused on cultivar rather than rootstock development because of the greater potential
gains by cultivar selection in native seedling populations. Rootstock development is
expected to be emphasized more when improved cultivars are released. There is
general agreement that the development of true-to type rootstocks for walnuts would
open a whole new realm of possibilities for the walnut growers. Dwarfing, greater
yields, precocity of production, and a reduction in variability of orchard trees have
been among the most often mentioned attributes (Balci et al., 2001).
31
T a b l e 3. Nut crop rootstocks propagated, percentage and quantity
of grafted plants produced in Turkey nurseries in 2005
3
l e n t e l ë. Rieðutø poskiepiai, Turkijos medelynuose 2005 metais áskiepytø
augalø procentas ir kiekis
Rootstocks
Fruit tree crops
Vaismedžiai
Poskiepiai
Number of grafted
plants
Áskiepytø augalø skaièius
%
units / vnt.
P. vera, P. khinjuk
P. terebinthus seedlings / P. terebinthus sëjinukai
100
19 100
Walnuts / Graikiniai riešutai Wild walnut seedlings / Laukiniø graikiniø riešutø
100
206 621
Pistachios / Pistacijos
sëjinukai
Conclusion. It may be stated that during the last decade, fruit growers in
Turkey improve their use of rootstocks in order to achieve better growth of temperate
fruit tree crops, better tolerance to unfavorable soil and phytosanitary problems,
improved dwarfing, and reduced management costs. The most recent crop to be
grafted on rootstocks in Turkey were walnut and almond, which always were grown
on their own roots until the end of the 1980s. It is expected that the next decade the
use of clonal rootstocks will be increased.
Gauta
2006 04 24
Parengta spausdinti
2006 07 13
References
1. A k ç a Y., C e y l a n S. A study on the comparison of some rootstock
properties of sweet and bitter almond seeds // Proceedings of Hazelnut and the Other Nut
Fruits Symposium, 10–11 January 1996, Samsun-Turkey. P. 402–408.
2. A n o n y m o u s. Statistical Yearbook of Turkey 2004, State Institute of Statistic
Prime Ministry Republic of Turkey, Publication Number: 2779, Ankara, Turkey, 2005.
3. A y y i l d i z T., A c i k e l S., K e s k i n A., A t s a n T. The
Relationship between Turkey and European Union // Publication of Ataturk University,
850, Erzurum, Turkey, 1997.
4. B a l c i A., B a l t a F., K a z a n k a y a A., S e n S. M. Promising
native walnut genotypes (Juglans regia L.) of the East Black Sea Region of Turkey //
Journal American Pomological Society. 2001. 55(4). P. 204–209.
5. E r c i s l i S., G u l e r y u z M., P a m i r M. Effects of different rootstocks
on fruit characteristics of some apple cultivars // Turkish Journal Agricultural Forestry.
2000. 24. P. 533–539.
6. E r c i s l i S. A short review of the fruit germplasm resources of Turkey // Genetic
Resources and Crop Evaluation. 2004. 51. P. 419–435.
7. F A O. Food and Agricultural Organization. 2005.www.fao.org.
8. G o n u l s e n N., O z v a r d a r S., B a l d i r a n E. The seed resources
for plum rootstocks. Proceedings of Seed Certification and Transportation Problems in
Turkey. TUBITAK. 1985. P. 585–590.
32
9. G u l e r y u z M. Temperate fruit species // Ataturk Univ. Agricultural Faculty.
1998. P. 128.
10. M c C a n d l e s s L. Cornell and USDA prospect for ‘Green Gold’ in the
mountains of Turkey//www.nysaes.cornell.edu/ pubs/ press /1999/ turkey.html.
11. M i s i r l i A., G u l c a n R., T a n r i s e v e r A. Importance of stomata
in evaluating the vigor of Prunus mahaleb rootstocks // Acta Horticultuýrae. 1996. 410,
P. 227–232.
12. U n a l A. Anatomy of the graft union and degree of incompatibility of some
apricot varieties budded on plum, almond and peach seedlings // Acta Horticulturae. 1992.
384. P. 493–496.
13. W a y R. D., A l d w i n c k l e H. S., L a m b R. C., R e j m a n A.,
S a n s a v i n i S., S h e n T. et al. Apples // Acta Horticulturae. 1990. 290. P. 1–63.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 27–33.
VIDUTINIO KLIMATO SÀLYGOMIS AUGANÈIØ VAISMEDÞIØ POSKIEPIAI
TURKIJOJE: APÞVALGA
S. Ercisli, A. Esitken, E. Orhan, O. Ozdemir
Santrauka
Daugelis sodo vaismedþiø Turkijoje yra skiepijami, iðskyrus graikinius rieðutmedþius
ir sedulas, kurie paprastai dauginami sëklomis. Pagrindiniai poskiepiai, á kuriuos turkø
augintojai mûsø laikais skiepija vidutinio klimato sàlygomis auganèius vaismedþius, yra
ðie: laukiniø obelø sëjinukai, M.9 ir MM.106 – obelims; laukiniø kriauðiø, ypaè Pyrus
eleagrifolia L., sëjinukai – kriauðëms; laukiniø persikø sëjinukai – persikams; laukiniø
slyvø sëjinukai – slyvoms; Mazzard ir Mahaleb sëjinukai, visai neseniai vegetatyviniu
bûdu pradëti dauginti poskiepiai Gisela 5 ir Gisela 6 – treðnëms; Juglans regia L.
sëjinukai – graikiniams rieðutmedþiams; laukiniø migdolø sëjinukai – migdolams; laukiniø
abrikosø sëjinukai – abrikosams. Vegetatyviniu bûdu dauginti poskiepiai vidutinio klimato
sàlygomis auganèiø vaismedþiø rûðims áskiepyti Turkijoje naudojami nepakankamai. Taèiau
pastaruoju metu ðalyje vis daugëja su vegetatyviniais poskiepiais áveistø sodø, ypaè
obelø ir vyðniø. Ðiame straipsnyje aptartas poskiepiø naudojimas vidutinio klimato
vaismedþiams áskiepyti Turkijoje.
Reikðminiai þodþiai: vidutinio klimato vaismedþiai, poskiepiø naudojimas, Turkija.
33
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 34–38.
ROOTSTOCKS OF FRUIT CROPS IN BELARUS
Vyacheslav SAMUS, Soltan GADZHIEV, Vitaliy POPLAVSKIY,
Nina DRABUDKO
RUE “Institute for Fruit Growing of the NAS of Belarus”, 2 Kovalev str.,
Samokhvalovitchy, Minsk region, Republic of Belarus.
E-mail: [email protected]
Biological and economic characteristics of recommended for cultivation and promising
clonal rootstocks of fruit crops according to the results of complex evaluation in stoolbed,
nursery and orchard in 1985–2005 are presented in the paper.
According to the complex indices the following apple rootstocks are recommended
for cultivation in the Republic: rootstocks PB-4, B.396, M.9, M.26, B.118, B.545, MM.10613. The following rootstocks are passed to the system of State variety trials: apple rootstock
106-13, plum rootstocks VPK-1, OD-2-3, VVA-1, cherry and sweet cherry AVCh-2, VSL-2,
Gisella-5, Damil GY-79.
Key words: clonal rootstocks, winterhardiness, vigor, biological, economic and
morphological characteristics, precocity, productivity, Belarus.
Introduction. Nowadays the most effective type of orchard is intensive onerow orchard planted on clonal rootstocks. The type of clonal rootstocks can change
the vigour, precocity, yield and resistance to biotic and abiotic factors of grafted
plants without impact on inheritance of cultivar properties (1).
The applied rootstock must be winter hardy, well-adapted to the environmental
conditions of the region, highly compatible with grafted cultivars, resistant to fungi
and virus diseases, gaining precocity, high yield and fruit quality as well as forming
compact trees for convenient maintenance and cropping (3).
According to the food standards adopted in the Republic of Belarus, gross
production of fruits and small fruits must be not less than 800 thousand ton per year.
Yearly gross production of fruits and small fruits was on the average 300–400
thousand ton during the last 5 years, which comprised 40–50% of the required
production.
Substantial increase of fruit production in the Republic may be possible in case
of creation of new orchards with dense plantation design. Intensification in horticulture
can be achieved by the use of dwarf clonal rootstocks (5). Early fruiting of such
trees allows shortening unproductive period and optimum planting density due to the
fact that compact trees makes land use of areas more effective, eventually gaining
high profits.
34
Materials and methods. The research was carried out at the Institute for Fruit
growing of the NAS of Belarus in 1985–2005.
Objects of research where the following groups of rootstocks:
35 forms of apple tree: B.118, B.396, V-9, B.476, B.545, 71-3-150, 71-3-195
(Russia, Michurinsk SAU); B-16-20, B-7-53 (Russia, Dagestan FBES); ARM-18
(Armenia, RIH&G); P1, P2, P14, P22, P59, P60 (Poland, Institute in Skierniewitse),
M.9 Emla, M.9 N-9-84, M.9 Rene Nikolaya, M.9 Pajam 1, M.9 Pajam-2 (England,
East Malling Research Station), Supporter-1, Supporter-3 (Germany, Institute of
Pomology at Dresden-Pillnitz), D-1161, D-471, D-1071, D-3331, D-2854,
Don-70-382, Don-70-362 (Ukraine, Artemovskiy HES), J-TE-E, J-TE-D, J-TE-F
(Czech republic); MM.106-13, PB-4 (Belarus, Institute for Fruit Growing of the
NAS of Belarus);
pear: 6 forms – Cydonia x oblonga BA-29 (France, INRA), quince ¹1/19, ¹1/22,
¹1/33 (Belarus, Institute for Fruit Growing of the NAS), SI-4-2 and SI-2-10 (Ukraine,
Research institute in Mliev named after L. P. Simirenko UAAS) and 7 forms of pear
rootstocks obtained from All-Russia Research Institute of Horticulture named after
I. V. Michurin (Russia) – pear-10, 217-24-4, 218-5-4, 218-6-4, 3-21-32, 218-4-4;
plum: 14 forms – 21-11, 21-20 (Russia, I.V.Michurin CSL at Michurinsk),
OD-2-3 (Russia, Voronezh State Agrarian University named after K. D. Glinka) ,
GF 655/2 (France, Research station La Grande Ferrade at Bordeaux), SVG 132-2,
SVG 11-19, 140-2, VPK-1 (Russia, All-Russia Research Institute of Siberia name
after M. A. Lisavenko at Barnaul), Gayovata, 9-250, 9-259, VVA-1, VSV-1,
VVA-146 (Russia, the Crimean Experimental Research Station RIP at Krymsk);
cherry and sweet cherry: 36 forms – P-1, OVP-2, OVP-3, OVP-4, OVP-5,
OVP-6, V-2-180, B-2-230, B5-88, C-8-101, Rubin (Russia, All Russia Research
Institute of Horticulture at Oriol), VC-13, LC-52, L-2, VSL-2, Mahrovaya-2,
Plakuchaya (Ukraine, the Crimean ERS), P-7, P-3–Moscovia, Izmaylovskiy (All Russia
Breeding and Technology Institute for Fruit Growing and Fruit Nurseries, Moscow,
Russia), AVCh-2 (Russia, All Russia Research Institute of Siberia named after M. A.
Lisavenko at Barnaul), Rossoshanskaya No.2, Rossoshanskaya No.3, Studenkovskaya
(the Ukraine, Artiomovskaya ESH), Gisella-5, F-1/12 (Germany), Damil GY-79
(Belgium), Meteor (the US), Oblachinskaya (Yugoslavia), 16-53, Antipka 18/19,
Antipka 18/20, 53/1, 9-78/23, 17/40, 14/2 18-1 (Belarus, Institute for Fruit Growing
of the NAS).
Research and observations were carried out according to „Programma i metodika
izucheniya klonovix podvoev v Pribaltiyskih respublikah i Byelorusskoy SSR” (Elgava,
1980).
Results. High winter hardiness was found in apple tree rootstocks B.118, B.396,
V-9, B.491, B.476, B.545, B-16-20, PB-4, B-3, D-1161, J-TE-E, MM.106-13; pear
rootstocks SI-4-2 and SI-2-10, pear-10, 3-21-32; plum rootstocks VPK-1, VVA-1,
GF 655/2, 140-2, OD-2-3, 9–250, VSV-1; cherry and sweet cherry rootstocks
OVP-2, B-2-230, B-2-180, C-8-101, LC-52, VSL-2, L-2, VSL-2, Izmaylovskiy,
Gisella-5, Damil GY-79.
The following rootstocks have the highest value and quality of stoolbed rooting:
apple rootstocks B.396, PB-4, ARM-18, B.491, B.118, B.476, B-7-35, B-16-20, pear-
35
quince VA-29, SI-2-10, plum rootstocks VPK-1, cherry and sweet cherry rootstock
VSL-2. The selected rootstocks provided the output of 15–20 rooted stoolbeds from
1 mother plant, rooting score was 4.5, trunk diameter at ground level – 7–11 mm,
mean length of stoolbed – 50–80 cm.
The following rootstocks were rooted worse (score 3.0): apple rootstocks M.9,
M.26, D1161, pear rootstocks SI4-2, plum rootstocks OD-2-3, cherry and sweet
cherry LC-52, L-2.
T a b l e. Economic and biological characteristics of adapted and
perspective clonal rootstocks of fruit crops
L e n t e l ë.
Ekonominës ir biologinës registruotø ir perspektyviø vegetatyviniø
poskiepiø charakteristikos
Rootstock
Vigour
Poskiepis
Augumas
Planting
density in
Propagation orchard,
method
tree/ha
Dauginimo
bûdas
Yield
during
Precocity,
full
year
fruiting Derëjimo
Derlius
visiško
derëjimo
metu, t/ha
pradžios
metai
2500
40
2
1666
32
2
2500
40
2
1666
32
2
1250
30
2
Sodinimo
sode
tankumas,
vaism./ha
Anchorage
Ásitvirtinimas dirvoje
Apple / Obelys
PB-4
Super-dwarf
Stoolbeds
Nykštukinis
Augynai
Dwarf
Stoolbeds
Weak, trellis
required
Silpnas, reikia atramø
B.396
Žemaûgis
Augynai
Weak, trellis
required
Silpnas, reikia atramø
M.9
Dwarf
Stoolbeds
Žemaûgis
Augynai
Semi-dwarf
Stoolbeds
Weak, trellis
required
Silpnas, reikia atramø
M.26
B.118
Pusiau þemaûgis
Augynai
Semi-vigorous Stoolbeds
Pusiau augus
Augynai
Trellis required
Reikia atramø
Good, trellis
temporary required
Geras, laikinai reikia
atramø
B.545
Semi-dwarf
Pusiau þemaûgis
Stoolbeds
1250
30
2
Augynai
Good, temporary
trellis required
Geras, laikinai reikia
atramø
MM.106-13
Semi-vigorous Stoolbeds
Pusiau augus
1250
35
2
Augynai
Good, temporary
trellis required
Geras, laikinai reikia
atramø
Pear / Kriauðës
VA-29
Semi-vigorous Stoolbeds
and
hardwood
cuttings
1250
Pusiau augus
20
3
Good, temporary
trellis not required
Geras,
nereikia laikinø atramø
Augynai ir
sumedëjæ
auginiai
36
T a b l e continued
L e n t e l ë s tæsinys
Rootstock
Vigour
Poskiepis
Augumas
Planting
density in
Propagation orchard,
method
tree/ha
Dauginimo
bûdas
Sodinimo
sode
tankumas,
vaism./ha
Yield
during
Precocity,
full
year
fruiting Derëjimo
Derlius
visiško
derëjimo
metu, t/ha
pradžios
metai
25
2
Anchorage
Ásitvirtinimas dirvoje
Plum / Slyvos
VVA-1
Dwarf
Softwood
and
hardwood
cuttings
2000
Softwood
and
hardwood
cuttings
1500
Semi-vigorous Softwood
cuttings
1250
Žemaûgis
Weak, trellis
required
Silpnas, reikia atramø
Žalieji ir
sumedëjæ
auginiai
OD-2-3
Semi-dwarf
Pusiau þemaûgis
20
2
Weak, trellis
required
Silpnas, reikia atramø
Žalieji ir
sumedëjæ
auginiai
VPK-1
20
2
Pusiau augus
Good, temporary
trellis not required
Geras, nereikia laikinø
atramø
Žalieji auginiai
Cherry and sweet cherry / Vyðnios ir treðnës
OVP-2
Semi-vigorous Softwood
Pusiau augus
cuttings
1250
Semi-vigorous Softwood
Pusiau augus
cuttings
1250
18
2
Žalieji auginiai
Ismaylovskiy
Geras, nereikia laikinø
atramø
18
Dwarf
Žemaûgis
Softwood
cuttings and
stoolbeds
2
Good, temporary
trellis not required
Geras, nereikia laikinø
atramø
Žalieji auginiai
VSL-2
Good, temporary
trellis not required
1666
22
Weak, trellis
required
Silpnas, reikia atramø
Žalieji auginiai
ir augynai
The following rootstocks have high rooting (85–100%) in propagation by
softwood cuttings: plum rootstocks OD 2-3, VPK-1, 140-2, 9-250, VVA-1, cherry
and sweet cherry rootstocks OVP-2, Izmaylovskiy, C-8-101, B-2-180, VSL-2,
AVCh-2.
Assessment of clonal rootstocks showed that the output of rootstock layers is
determined by both meteorological conditions during vegetative period and biological
specifics of rootstocks. Maximum output of standard rootstocks (75–88%) was
found for the rootstocks of apple – B.396, B.118, ARM-18, B-7-35, B.476, J-TE-E,
pear-quince VA-29, plum VPK-1, cherry and sweet cherry OVP-2, Ismaylovskiy,
37
VSL-2, LC-52, B-2-180, C-8-101.
The following rootstocks were distinguished by precocity and yield efficiency:
apple rootstocks PB-4, B.396, M.9, M.26, ARM-18, B-7-35, B-16-20, B.118, B.545;
pear-quince VA-29; plum VPK-1; cherry and sweet cherry OVP-2, Ismaylovskiy,
B-2-230 [2,4].
Conclusions. According to the complex indices the following apple rootstocks
are recommended for cultivation in the Republic: rootstocks PB-4, B.396, M.9, M.26,
B.118, B.545, MM.106-13. The following rootstocks are passed to the system of
State variety trials: apple rootstock 106-13, plum rootstocks VPK-1, OD-2-3,
VVA-1, cherry and sweet cherry AVCh-2, VSL-2, Gisella-5, Damil GY-79.
Gauta
2006 05 09
Parengta spausdinti
2006 08 03
References
1. B u d a g o v s k i y V. I. Kultura slaboroslih plodovih derevyev. Moscow.
1976. 303. (in Russian).
2. D r a b u d k o N. N. Rezultati izuchenija klonovih podvoyev vishni I chereshni
v pitomnike: mat. II mezhdunarodnogo simposiuma, posviashchonnogo 80-letiyu so dnia
rozhdeniya A.S. Deviatova // Ekologicheskaya otsenka tipov visokoplotnih plodovih
nasazhdeniy na klonovih podvoyah. Samokhvalovichy. 12–15 avgusta 2003. P.149–152.
(in Russian)
3. Y e r e m i n G. V. Kostochkoviye kulturi. – Rostov-na-Donu. 2000. 254. (in
Russian)
4. Z h a b r o v s k i y I. E. Hoziaystvenno-biologicheskie osobennosti novih
klonovih podvoev yabloni v usloviyah Respubliki Belarus: Diss. kand. s.-h. nauk: 1999.
06.01.07. p. Samokhvalovichy Minskoy obl. 143. (in Russian)
5. T s y n g a l e v N. M. Klonoviye podvoi slivy: sbornik nauchnih trudov //
Slaborosliye klonoviye podvoi v sadovodstve. Michurinsk. 1997. 149. (in Russian)
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 34–38.
VAISMEDÞIØ POSKIEPIAI BALTARUSIJOJE
V. Samus, S. Gadzhiev, V. Poplavskiy, N. Drabudko
Santrauka
Ðiame darbe pateiktos biologinës ir ekonominës rekomenduojamø auginti ir
perspektyviø vegetatyviniø poskiepiø charakteristikos remiantis 1985–2005 metais atlikto
vertinimo poskiepiø dauginimo augyne, medelyne ir sode rezultatais. Kompleksiðkai
ávertinus, auginti Baltarusijoje rekomenduoti ðie obelø poskiepiai : PB-4, B.396, M.9, M.26,
B.118, B.545, MM.106-13. Á valstybinius veisliø tyrimus átraukti ðie poskiepiai: obelø
poskiepis 106-13, slyvø poskiepiai – VPK-1, OD-2-3, VVA-1, vyðniø ir treðniø poskiepiai –
AVCh-2, VSL-2, Gisella-5, Damil GY-79.
Reikðminiai þodþiai: vegetatyviniai poskiepiai, atsparumas ðalèiui, augumas,
biologinës, ekonominës ir morfologinës charakteristikos, ankstyvumas, derlingumas,
Baltarusija.
38
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 39–46.
GROWTH AND QUALITY OF PEAR MAIDEN TREES
DEPENDING ON ROOTSTOCK AND GROWING SEASON
Jacek LEWKO1, Andrzej SADOWSKI2, Kazimierz ÚCIBISZ3
Department of Pomology, Warsaw Agricultural University – SGGW,
Nowoursynowska 159, 02-776 Warsszawa, Poland.
E-mails: 1 [email protected]; 2 [email protected];
3
[email protected]
The aim of the trial was to assess the influence of five rootstocks on vigour of two
pear cultivars under different weather conditions in Central Poland. Diameter of rootstock
and maiden tree trunk, tree height as well as feathering of maiden trees were evaluated. All
parameters of trees raised in 2003, except for tree height, were higher than those of trees
raised in 2004. Cv. ‘Erika’ produced taller and more branched, but thinner trees than
‘Conference’. Both Pyrus rootstock, seedlings of Caucasian pear and Pyrodwarf, induced
a higher vigour and better branching than any Cydonia rootstock. No significant
differences were found within the rootstocks groups.
Key words: Cydonia, growth, nursery stock, pear, Pyrus, quince, rootstock, tree
quality.
Introduction. Importance of pear as a fruit crop is recently increasing in Poland.
Quality of planting stock is determining the success of a modern orchard. Selection
of a proper rootstock is essential in that respect. Limited information is available,
however, concerning rootstocks for pear, their growth in nursery and influence on
quality of nursery stock. In Poland, seedlings of Caucasian pear (Pyrus communis
var. caucasica Fed. syn. Pyrus communis ssp. caucasica (Fed.) Browicz) are most
commonly used. Recently seedlings of pears of unknown origin are being replaced
by seedlings of three seed cultivars, ‘Belia’, ‘Doria’ and ‘Elia’, selected at the Institute
of Pomology and Floriculture in Skierniewice.
Intensive pear orchards in Poland are planted on quince clones, MA – a standard,
semi-dwarfing rootstock selected by Hatton in East Malling, England and on S 1 – a
Polish selection of Somorowski (1964). The latter has been recognised as more
winter hardy, compared with the standard Hatton’s selections, MA and MC
(Somorowski, 1964; Grzyb, 1987; Hoùubowicz and Bojar, 1995). It may also increase
winter hardiness of pear grown on this rootstock (Iwanszyniec and Hoùubowicz,
1998). Quince S 1 for many years was considered as more invigorating in the orchard,
compared with the quince MA (Grzyb, 1987). However, recently no differences in
39
vigour between young pear trees grown on quince S 1 and quince MA (Sosna, 2000)
or on quinces S 1, MA and MC (Iwaniszyniec and Hoùubowicz, 1998) were found.
This rootstock was also tested in Czech Republic (Kobìluð, personal communication),
however, only its effect on bud take of different pear cultivars has been reported to
date, (Kobìluð and Øeznièek, 2004). Lately a new rootstock originated from Pyrus
communis, named Pyrodwarf, was selected by Jacob (1998). It was described as
dwarfing and, because of the fact that it is a cross between two pear cultivars, no
incompatibility problem should occur. Growing season influences vigour and quality
of nursery stock of apples and sour cherries grown on the same soil and rootstock
as shown by Lipecki and Janisz (2004).
Materials and methods. The trial was set up in two successive series, in
Warsaw-Wilanów, on a silty loam alluvial soil of post-glacial valley of Vistula River.
In the spring of 2002 and 2003 the following rootstocks were planted in the nursery:
Caucasian pear seedlings, Pyrodwarf, quince S 1, quince MA and quince MC. All
rootstocks were well rooted and of grade 6–8 mm at collar root. To prevent infection
of Agrobacterium tumefaciens, roots were treated with Polagrocyna PC
(Agrobacterium radiobacter, strain K84). The planting distance was 30 cm in row
and 75 cm between rows. In each two-year nursery cycle standard nursery practices
were carried out, except for treatments promoting feathering of maiden trees. At the
beginning of August, in the year of planting, rootstocks of pear cultivars ‘Conference’
and ‘Erika’ were chip-budded at the height of 10 cm. At the end of September of the
second year of each cycle, diameter of rootstock (5 cm above the ground), trunk
diameter (10 cm above bud union) and tree height were measured. Number and
length of lateral branches (feathers) was also recorded and the percentage of
spontaneously branched (feathered) trees calculated.
Weather conditions of the second year of nursery cycle differed in two series
of the trial. The most distinct were the differences of mean temperatures (Table 1).
The beginning of 2004 (February-April) was warmer than that of 2003. However,
later (May-July), mean monthly temperatures were much higher in 2003 than in
2004. Temperatures at the end of the growing season (August-September) did not
differ in these two years. Monthly rainfall was less important, as the overhead irrigation
was regularly applied.
The trials were set up in a randomised block design, in 5 replications, with 25
plants per each cultivar/rootstock plot. The data were subjected to analysis of variance.
For comparison of treatments means the F-test (for two means) or Newman-Keuls
(for more than two means) was applied, at α = 0.05. The percentage of branched
plants was transformed, prior to analysis, using the formula of Bliss (y = arcsin√x);
in tables the retransformed data are shown.
40
T a b l e 1. Mean monthly temperatures (°C) and their difference
between 2003 and 2004
1
l e n t e l ë. Vidutinës mënesio temperatûros (°C) ir jø skirtumai 2003 ir 2004
metais
Month
1971–2000
2003
2004
January / Sausis
-2.2
-2.4
-4.1
Mënuo
Difference, 2003–2004
ir 2004 m.
Skirtumas 2003
1.7
February / Vasaris
-1.2
-4.4
0.9
-5.3
March / Kovas
2.6
2.6
4.4
-1.8
April / Balandis
7.9
7.7
9.3
-1.6
May / Geguþë
13.7
16.1
12.8
3.3
June / Birželis
16.5
18.8
16.6
2.2
July / Liepa
18.1
21.2
18.6
2.6
August / Rugpjûtis
17.7
19.9
19.8
0.1
September / Rugsëjis
13.0
14.8
14.5
0.3
October / Spalis
8.1
6.1
10.7
-4.6
November / Lapkritis
2.8
5.5
4.4
1.1
December / Gruodis
-0.4
1.8
2.5
-0.7
Mean of year / Metø vidurkis
8.1
9.0
9.2
-0.2
Results and discussion. As all types of rootstocks were of similar size (grade
6–8 mm) at planting, the rootstock diameter at the end of the experiment might serve
as an indicator of the two-year growth in the nursery. In general, the rootstock
diameter at the end of the first nursery cycle (in the autumn of 2003) was larger than
that at the end of the second cycle (in 2004) – Table 2. Cultivar did not influence the
rootstock diameter (Table 3). Some differences in growth of particular rootstocks
depending on nursery cycle were noted (Table 5); after the first nursery cycle both
rootstocks of Pyrus origin had significantly larger diameter compared with the Cydonia
rootstocks, whereas after the second cycle a significant difference was found only
between the Pyrus rootstocks and quince MC.
The main index of vigour and quality of a nursery tree is its trunk diameter.
Similarly to the diameter of rootstock, trees raised in the first cycle (dug out in 2003)
had thicker trunks than those of the second cycle (dug out in 2004) – Table 2.
‘Conference’ developed trees with a larger diameter than ‘Erika’ (Table 3) in both
series of the trial. This corresponds to the results obtained by Kobìluð and Øeznièek,
(2004).
41
T a b l e 2. Indices of vigour and quality of nursery trees as affected
by the growing season; mean values for five rootstocks
and two cultivars
2
l e n t e l ë.
Trial series
Bandymø serija
2002–2003
2003–2004
Significance of
difference
Sodinamosios medþiagos augumas ir kokybës rodikliai,
priklausomai nuo augimo sezono; vidutinës penkiø poskiepiø ir
dviejø veisliø reikðmës
Rootstock
diameter
Trunk
diameter
Poskiepio
skersmuo,
Kamieno
skersmuo,
mm
mm
20.7
18.1
Maiden
tree height
Sodinuko
aukštis, cm
14.6
12.6
178.4
174.6
**
ns
**
Total
length of
laterals
Bendras
ðoniniø ðakø
ilgis, cm
180.0
89.6
Percentage
Number of
of branched
laterals
trees
Ðoniniø ðakø
skaièius
4.8
2.4
**
Ðakotø
sodinukø, %
82.1
33.0
**
**
Skirtumo patikimumas 1
1
Based on F-test: ns – non-significant / Pagrásta F-testu: ns – nepatikima; ** significant at
α = 0.01 / patikima, kai α = 0,01
T a b l e 3. Indices of tree vigour and quality depending on cultivar;
mean values of five rootstocks and two series of the trial
3
l e n t e l ë.
Cultivar
Veislë
‘Erika’
‘Conference’
Significance of
difference
Skirtumo patikimumas 1
1
Vaismedþio augumo ir kokybës rodikliø priklausomumas nuo
veislës; vidutinës penkiø poskiepiø ir dviejø bandymø serijø
reikðmës
Rootstock Trunk
diameter diameter
Maiden Total length Number Percentage of
tree height of laterals of laterals branched trees
Poskiepio
skersmuo,
Kamieno
skersmuo,
mm
mm
18.9
19.8
13.0
14.3
189.1
163.9
ns
**
**
Sodinuko Bendras ðoniniø
aukštis, cm ðakø ilgis, cm
177.7
91.9
**
Ðoniniø
ðakø
skaièius
4.9
2.2
**
Ðakotø sodinukø,
%
77.3
38.6
**
For explanations see Table 2. / Paaiðkinimà þr. 2 lentelëje
Growing season did not influence the height of maiden trees (Table 2). Trees of
cv. ‘Erika’ were higher than trees of ‘Conference’ (Table 3). Trees on both Pyrus
rootstocks were higher, compared with those on Cydonia rootstocks (Table 4). In
case of tree height no significant differences between quince rootstocks were found
either. This confirms the results of Lepsis et al. (2004); in their trials no differences
between height of trees raised on quinces MA and MC were found. Similar results
with ‘Conference’ were obtained by Sosna and Gudarowska (1995). In the study of
Kviklys (2000) maidens on quince MC were higher than on quince MA.
42
T a b l e 4. Trunk diameter and height of maiden tree depending on
the type of rootstock; mean values of two cultivars and two
series of the trial
4
l e n t e l ë.
Sodinuko kamieno skersmens ir aukðèio priklausomumas nuo
poskiepio rûðies; vidutinës dviejø veisliø ir dviejø bandymø serijø
reikðmës
Tree height
Trunk diameter
mm Vaismedžio aukštis, cm
Rootstock type
Poskiepio rûðis
Kamieno skersmuo,
Caucasian pear seedling / Kaukazietiðkos kriauðës
15.0 b1
sëjinukas
195.1 b
Pyrodwarf
15.2 b
193.4 b
Quince S 1 / Svarainis S 1
12.4 a
163.8 a
Quince MA / Svarainis MA
12.9 a
165.5 a
Quince MC / Svarainis MC
12.6 a
164.8 a
Values followed by the same letter do not differ significantly; Newman-Keuls test at α = 0.05
Ta paèia raide paþymëtos reikðmës ið esmës nesiskiria; Newman-Keuls testas, kai α = 0,05.
1
T a b l e 5. Rootstock diameter, number and total length of lateral
branches depending on the type of the rootstock and
growing season; mean values of two cultivars
5
l e n t e l ë.
Poskiepio skersmens, ðoniniø ðakø skaièiaus ir bendro ilgio
priklausomumas nuo poskiepio rûðies ir augimo sezono; vidutinës
dviejø veisliø reikðmës
Rootstock type
Poskiepio rûðis
Total length of laterals
Rootstock diameter
Number of laterals
Bendras ðoniniø ðakø ilgis,
Ðoniniø ðakø skaièius
mm
cm
Poskiepio skersmuo,
2003
2004
2003
2004
Caucasian pear seedling
24.4 b1
19.9 b
320.5 b
163.3 b
7.5 b
4.1 b
Pyrodwarf
24.3 b
20.5 b
310.6 b
181.3 b
7.4 b
4.1 b
Quince S 1 / Svarainis S 1
18.2 a
17.2 ab
76.7 a
23.8 a
2.7 a
0.9 a
Quince MA / Svarainis MA
18.4 a
17.4 ab
95.6 a
38.3 a
3.4 a
1.3 a
Quince MC / Svarainis MC
18.2 a
15.5 a
96.7 a
41.5 a
3.2 a
1.4 a
Kaukazietiðkos kriauðës sëjinukas
1
2003
2004
For explanations see Table 4 / Paaiðkinimà þr. 4 lentelëje
All indices of branching, i.e. number and total length of laterals as well as
percentage of spontaneously branched (feathered) trees, were higher in 2003 than in
2004 (Table 2). May, June and July of 2003 were warmer than in the next year
(Table 1). This was obviously the reason for a more vigorous growth and more
abundant feathering, as shown in Table 2. In both series of our trial, trees of cv.
‘Erika’ were better branched that trees of ‘Conference’ (Tables 3 and 7). All indices
of branching were higher when Pyrus rootstocks were used (Tables 5 and 6). Little
information about feathering of pear trees in the nursery is available in the literature.
43
Poniedziaùek and Porêbski (1995) mentioned that ‘Conference’ on a seedling rootstock
shows a very low percentage of feathered trees; feathering in their study was lower
than in our trial. Sosna and Gudarowska (1995) reported that ‘Conference’ on quince
rootstocks branched poorly.
T a b l e 6. Number of lateral branches and percentage of branched
trees depending on rootstock and cultivar; mean of two
series of the trial
6
l e n t e l ë.
Poskiepio ir veislës átaka ðoniniø ðakø skaièiui ir iðsiðakojusiø
vaismedþiø procentui; dviejø bandymø serijø vidurkiai
Number of laterals
Rootstock
Ðoniniø ðakø skaièius
Poskiepis
‘Erika’
‘Conference’
Percentage of branched trees
Ðakotø sodinukø procentas
‘Erika’
‘Conference’
Caucasian pear seedling
7.6 b1
4.1 b
90.6 b
73.9 b
Pyrodwarf
7.5 b
4.0 b
96.9 b
82.0 b
Quince S 1 / Svarainis S 1
2.7 a
0.8 a
54.6 a
14.3 a
Kaukazietiðkos kriauðës sëjinukas
Quince MA / Svarainis MA
3.3 a
1.4 a
65.5 a
17.2 a
Quince MC / Svarainis MC
3.6 a
0.9 a
65.8 a
13.2 a
1
For explanations see Table 4 / Paaiðkinimà þr. 4 lentelëje
T a b l e 7. Total length of lateral branches and number of laterals
depending on cultivar and growing season; mean values of
five rootstocks
7
l e n t e l ë.
Bendro ðoniniø ðakø ilgio ir skaièiaus priklausomumas nuo veislës
ir augimo sezono; vidutinës penkiø poskiepiø reikðmës
Series of the trial
Bandymø serijos
Total length of laterals
Bendras ðoniniø ðakø ilgis, cm
‘Erika’
2002–2003
2003–2004
Significance of difference1
Skirtumo patikimumas
1
‘Conference’
236.4
119.0
123.6
60.3
**
**
Number of laterals
Ðoniniø ðakø skaièius
‘Erika’
6.6
3.3
**
‘Conference’
3.1
1.4
**
For explanations see Table 2 / Paaiðkinimà þr. 2 lentelëje
Conclusions. 1. Vigour and quality of pear nursery stock depend on weather
conditions; warmer beginning of a growing season favours both – vigour and feathering
of maiden trees.
2. Rootstocks originated from pear induce stronger growth in the nursery,
followed by a higher quality of nursery stock. Pyrodwarf, described as dwarfing
rootstock, induces the same vigour of trees in the nursery as the standard seedling
rootstock. There are no differences between growth and final quality of trees on
different quince rootstocks.
44
3. ‘Erika’ produces thinner but taller and better-branched trees than ‘Conference’.
Vigour and quality of tree of any cultivar may be, however, considerably modified by
rootstock.
Gauta
2006 05 05
Parengta spausdinti
2006 07 17
References
1. G r z y b Z. Cechy odróýniajàce klony pigwy u¿ywane na podk³adki dla gruszy
// Ogrodnictwo. 1987. (3). P. 6–7.
2. H o ù u b o w i c z T., B o j a r K. Wytrzymaùoúã na mróz jednorocznych
pædów trzech typów pigwy (Cydonia oblonga Mill.) // Prace Komitetu Nauk Rolniczych i
Leúnych PTPN, Prace z Zakresu Nauk Rolniczych (Poznañ). 1995. Vol. 79. P. 179–185.
3. I w a n i s z y n i e c P., H o ù u b o w i c z T. Wzrost, plonowanie i
mrozoodpornoúã drzew w intensywnym sadzie gruszowym // Zeszyty Naukowe Akademii
Rolniczej w Krakowie. 1998. Vol. 333. P. 439–443.
4. J a c o b H. Pyrodwarf, a new clonal rootstock for high density pear orchards //
Acta Horticulturae. 1998. Vol. 475. P. 169–177.
5. K o b ì l u ð V., Ø e z n i è e k V. Cydonia Mill. as a pear rootstock and their
influence on the quality of pear nursery stock. ISHS 8 th International Symposium on
Integrated Canopy, Rootstock and Environmental Physiology in Orchard Systems
(Budapest, Hungary, 13–18. 06.2004), Book of Abstracts. 2004. P. 115.
6. K v i k l y s D. Paprastojo svarainio (Cydonia oblonga Mill.) sëkliniai poskiepiai
kriauðëms // Lietuvos sodininkystës ir darþininkystës instituto ir Lietuvos þemës ûkio
universiteto mokslo darbai. Sodininkystë ir darþininkystë. Babtai, Lithuania, 2000.
Vol. 19(2). P. 23–25.
7. L e p s i s J., D r u d z e I., D e k e n s U. The evaluation of different plum
and pear rootstocks in the nursery // Acta Horticulturae. 2004. Vol. 658(1). P. 167–172.
8. L i p e c k i J., J a n i s z A. Wzrost okulantów róýnych gatunków drzew
owocowych w zaleýnoúci od niektórych warunków úrodowiska // Annales Universitatis
Mariae Curie-Skùodowska Lublin – Polonia, Sectio EEE. 2004. Vol. XIV. P. 45–54.
9. P a r r y M. S. Trials of dwarfing quince rootstocks with Comice and Conference
pears // Journal of Horticultural Sciences. 1981. Vol. 56(2). P. 139–143.
10. P o n i e d z i a ù e k W., P o r æ b s k i S. Wpùyw sposobu traktowania
okulantów jabùoni i gruszy na ich rozgaùæzianie siæ i wzrost // Zeszyty Naukowe AR w
Krakowie. 1995. Vol. 302. P. 59–68.
11. S o m o r o w s k i K. Nowe typy pigwy podkùadkowej // Prace Instytutu
Sadownictwa w Skierniewicach. 1964. Vol. 8. P. 21–29.
12. S o s n a I. Wpùyw dwóch klonów pigwy oraz dwóch sposobów prowadzenia
drzew na wzrost i owocowanie kilku odmian gruszy // Zeszyty Naukowe Instytutu
Sadownictwa i Kwiaciarstwa w Skierniewicach. 2000. Vol. 8. P. 209–216.
13. Sosna I., Gudarowska E. Typy pigwy – opinie, badania // Szkóùkarstwo (3). 1995.
P. 23–24.
45
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 39–46.
KRIAUÐIØ SODINUKØ AUGIMO IR KOKYBËS PRIKLAUSOMUMAS NUO
POSKIEPIØ IR AUGIMO SEZONO
J. Lewko, A. Sadowski, K. Úcibisz
Santrauka
Bandymo tikslas buvo ávertinti penkiø poskiepiø átakà dviejø kriauðiø veisliø augumui
skirtingomis klimato sàlygomis centrinëje Lenkijoje. Buvo ávertintas poskiepio ir sodinuko
kamieno skersmuo, vaismedþio aukðtis ir sodinukø ðakojimasis. Visi 2003 metais iðaugintø
sodinukø augimo rodikliai, iðskyrus vaismedþio aukðtá, buvo geresni uþ 2004 metais
iðaugintø vaismedþiø augimo rodiklius. ‘Erika’ veislës kriauðës buvo aukðtesnës ir
ðakotesnës, bet plonesnio kamieno uþ ‘Conference’ veislës kriauðes. Pyrus poskiepiai,
kaukazietiðkos kriauðës ir Pyrodwarf sëjinukai lëmë geresná augumà ir ðakojimàsi negu bet
kuris Cydonia poskiepis. Tarp poskiepiø grupiø esminiø skirtumø neaptikta.
Reikðminiai þodþiai: Cydonia, augimas, sodinukai, kriauðës, Pyrus, svarainiai,
poskiepiai, vaismedþiø kokybë.
46
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 47–51.
BUD-TAKE AND MAIDEN TREE PARAMETERS OF TWO
APRICOT CULTIVARS BUDDED ON DIFFERENT
SEEDLING ROOTSTOCKS
Miroslaw SITAREK, Tadeusz JAKUBOWSKI
Research Institute of Pomology and Floriculture, Pomologiczna 18, 96-100
Skierniewice, Poland. E-mails: [email protected], [email protected]
Bud-take and growth of apricot cultivars ‘Morden 604’ and ‘LAK 101’ budded on
seedling rootstocks Wangenheim Prune (P. domestica L.), Erunosid (P. domestica L.), A.4
(P. armeniaca L.) and M.46 (P. armeniaca L.) were compared with seedlings P. cerasifera
var. divaricata Borkh. as the control.
The effectiveness of budding was high and varied from 88.8% to 97.2% depending
on rootstock/cultivar combinations. However, rootstock had no significant influence on
the number of budded trees produced in the nursery. Apricot seedlings A.4 and M.46
gave very high quality maidens. The one-year-old apricot trees budded on these rootstocks
were significantly higher and thicker than trees on P. divaricata. The trees of both cultivars
tested on Wangenheim Prune and Erunosid were weaker in terms of all grow parameters
than those grafted on P. divaricata.
Key words: apricot, rootstock, cultivar, growth in a nursery.
Introduction. Seedlings from different local biotypes of apricot are the most
widely used rootstocks for apricot trees in the Mediterranean basin and in the rest of
South European countries (Indreias et al., 2004; Orero et al., 2004). For lower scale
there are also used myrobalan, plum, almond and peach seedlings. For example,
myrobalan as a rootstock for apricot trees is often used in Romania, Yugoslavia,
Bulgaria, Czech Republic and France (Audergon et al., 1991; Dimitrova and Marinov,
2002; Vachun, 1995). In Poland P. seedling divaricata Borkh. is still the most popular
rootstock not only for plum trees, but for apricot cultivars too (Grzyb et al., 1996;
Jakubowski, 2004). However, using this rootstock is sometimes risky because not
all cultivars are physiologically compatible with it. Incompatibility between scion
cultivars and P. divaricata rootstock (within apricot in Polish growing conditions) is
very often expressed by rapid death of trees a few years after planting in the orchard
or easy break down at the graft union (Grzyb et al., 1996; Jakubowski, 2004).
Therefore more intensive searching was undertaken for selection of new seedling
rootstocks, having good compatibility with apricot cultivars, reducing growth of
trees and good adaptability to cool climate of Poland.
47
The aim of this paper was to evaluate bud-take and growth of maiden trees of
two apricot cultivars grafted on five seedling rootstocks in the nursery field.
Materials and methods. The field experiment was established in the Andrzej
Nowakowski nursery in Zdzary (Central Poland) on podzolic soil overlaying loose
sand boulder loam. It was designed in a multifactor system composed of separate
experiments repeated in three consecutive years. The first rootstocks were planted
in 2002, the last – in the spring of 2004. Seedling rootstocks Wangenheim Prune
(P. domestica L.), Erunosid (P. domestica L.), A.4 (P. armeniaca L.), M.46
(P. armeniaca L.) were compared with seedlings P. cerasifera var. divaricata Borkh.
The rootstocks were chip-budded with cultivars ‘Morden 604’ and ‘LAK 101’ at the
end of July. The buds were placed about 10 cm above ground level and wrapped
with foil strips. The strips were removed 5 weeks after budding.
The experiment was set up with four replications in randomised block design.
Each cultivar/rootstock combination was represented by 100 plants (25 x 4 replicates),
planted in the nursery at a distance of 0.9 x 0.25 m. Standard cultural and protective
practices provided for nursery production were used throughout the experiment.
At the end of October buds taken were counted and in the subsequent spring
their survival was evaluated. Before digging out the trees, their height, total length of
side shoots and trunk diameter 20 cm above the budding place was measured. During
vegetation period all side shoots were removed till 50 cm of height.
The results were processed using a statistical analysis of variance. To evaluate
the significance of mean differences within each cultivar the Duncan’s Multiple Range
test was used at P=0.05.
Results and discussion. Each year of the experiment, the number of successful
bud-takes evaluated in the autumn was close to shoots sprouted in the spring and to
the number of one-year-old trees obtained at the end for each cultivar/rootstock
combination. Fortunately, no winter damages were observed. Therefore, only mean
data on the number and quality of one-year-old trees for the 2003–2005 seasons are
presented.
The effectiveness of budding was high and varied from 88.8% to 97.2%
depending on rootstock/cultivar combinations. However, rootstock had some, but
no significant influence on the number of budded trees produced (Table). Apricot
seedlings A.4 and M.46 caused very high maiden quality. The one-year-old apricot
trees budded on these rootstocks were significantly higher and thicker than trees on
P. divaricata. The trees of both cultivars tested on Wangenheim Prune and Erunosid
were weaker in terms of all grow parameters than those grafted on P. divaricata.
Small size of one-year-old trees in a nursery can give the evidence of a dwarfing
effect of the rootstock. For example, this is observed in sweet cherry trees grafted
on dwarfing rootstocks (Sitarek and Grzyb, 1998). However, it can inform sometimes
about their physiological incompatibility. Grzyb et al. (1996) reported that usefulness
of seedlings Wangenheim Prune for apricot is very limited due to short life duration
of trees in the orchard, although that rootstock effectively depress tree growth.
Likely, using rootstocks belonging to P. domestica for apricot under Polish growing
conditions is risky. However, symptoms of rootstock/scion incompatibility of apricot
varieties on peach and myrobalan seedling rootstocks may occur too (Bassi, 1999;
48
Lapins, 1959; Southwick et al., 1999; Suranyi, 1999). Therefore, further investigations
are necessary to draw the last conclusions. For this purpose the produced trees
were planted in the orchard and the new experiment with influence of rootstocks on
the growth and yield of apricot trees was established.
T a b l e. Characteristic of apricot trees budded on different seedling
rootstocks, mean values for 2003–2005
L e n t e l ë.
Abrikosø, áskiepytø á skirtingus sëklinius poskiepius, charakteristika,
2003–2005 m. vidurkiai
Number of
maiden trees
Cultivar and
rootstock
Sodinukø
skaièius
Tree height
Vaismedžio
aukštis
Trunk diameter
Kamieno
skersmuo
Veislë ir
poskiepis
No./25
%
cm
%
mm
%
Total length
of side
shoots
Bendras ðakø
ilgis
cm
%
P. divaricata
Wangenheim
Prune
A.4
M.46
Erunosid
23.4
23.5
‘Morden 406’
93.6 197.6 100.0 16.2 100.0 359 100.0
94.0 179.5 90.8 14.5 89.5 278 77.4
24.0
23.4
23.0
96.0 189.9 96.1 17.1 105.6 490 136.5
93.6 216.3 109.5 17.1 105.6 643 179.1
92.0 173.0 87.5 13.8 85.2 255 71.0
LSD0.05
2.5
9.5
1.4
56.6
Number of
side shoots
Ðakø skaièius
per
tree
vieno
medžio
%
Mean
length of
side shoot
Vidutinis
šakos ilgis
cm
%
7.5
6.1
100.0 47.7 100.0
81.3 45.6 95.6
10.1
12.2
6.5
134.7 48.5 101.7
162.7 52.7 110.5
86.7 39.2 82.2
1.6
5.8
‘LAK 101’
P. divaricata
Wangenheim
Prune
A.4
M.46
Erunosid
22.2
23.8
88.8 201.9 100.0 15.2 100.0
95.2 171.3 84.8 12.2 80.3
289
115
100.0
39.8
6.2
4.0
100.0 46.6 100.0
64.5 28.8 61.8
23.8
24.3
23.4
95.2 210.1 104.1 15.0 98.7
97.2 222.1 110.0 16.5 108.5
93.6 189.0 93.6 13.8 90.8
389
490
228
134.6
169.6
78.9
9.1
9.9
6.1
146.8 42.7 91.6
159.7 49.5 106.
98.4 37.4 80.2
LSD0.05
2.4
1.5
6.4
10.2
1.3
45.4
Conclusions. Rootstocks tested had no significant effect on bud-take of apricot
cultivars in a nursery. Size of one-year-old apricot trees was depended on rootstock
type. In comparison to seedlings P. divaricata, apricot seedlings A.4 and M.46 gave
maidens of higher quality. The trees budded on Wangenheim Prune and Erunosid
were weaker in terms of all grow parameters than those on P. divaricata.
Gauta
2006 02 02
Parengta spausdinti
2006 08 03
49
References
1. A u d e r g o n J. M., D u q u e s n e J., N i c o l a s J., C a u d u b e r t
A. New selected rootstocks for apricot cultivars: Torinel. Acta Hort. 1991. 293. P. 395–400.
2. B a s s i D. Apricot culture: Present and future. Acta Hort. 1999. 293. P. 395–400.
3. D i m i t r o v a M., M a r i n o v P. Myrobalan (P. cerasifera Ehrh.) as a
rootstock for apricot. Acta Hort. 2002. 577. P. 315–318.
4. G r z y b Z. S., Z d y b H., S i t a r e k M. Wpùyw róýnych podkùadek na
zdrowotnoúã, siùæ wzrostu i owocowanie moreli. Zesz. Nauk. ISiK 1996. 3. P. 55–62.
5. I n d r e i a s A., S t e f a n I., D u t u I. Apricot rootstocks created and
used in Romania. Acta Hort. 2004. 658. P. 509–511.
6. J a k u b o w s k i T. Uprawa moreli. Wydawnictwo Hortpress Sp. z o. o.,
Warszawa, 2004.
7. L a p i n s K. Some symptom of stock scion incompatibility of apricot varieties
on peach seedling rootstock. Can. J. of Pl. Sci., 1959. 39. P. 194–203.
8. O r e r o G., C u e n c a J., R o m e r o C., M a r t i n e z - C a l v o J.,
B a d e n a s M. L., L l a c e r G. Selection of seedling rootstocks for apricot and
almond. Acta Hort. 2004. 658. P. 529–533.
9. S i t a r e k M., G r z y b Z. S. Bud-take and growth of sweet cherry trees
budded on different rootstocks. J. of Fruit and Ornamental Plant Research. 1998. 1.
P. 23–31.
10. S o u t h w i c k S. M., W e i s K. G. Propagation and rootstocks for
apricot production. Acta Hort. 1999. 488. P. 403–410.
11. S u r a n y i D. Wild apricot and myrobalan generative rootstocks for apricot
cultivars. Acta Hort. 1999. 488. P. 445–449.
12. V a c h u n Z. Rootstocks for apricot – the current situation and main problems.
Acta Hort. 1995. 384. P. 459–465.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 47–50.
DVIEJØ ABRIKOSØ VEISLIØ, ÁSKIEPYTØ Á SKIRTINGUS SËKLINIUS
POSKIEPIUS, PRIGIJIMAS IR SODINUKØ AUGIMO RODIKLIAI
M. Sitarek, T. Jakubowski
Santrauka
‘Morden 604’ ir ‘LAK 101’ veisliø abrikosø, áskiepytø á Wangenheimo vengrinës
(P. domestica L.), Erunosid (P. domestica L.), A.4 (P. armeniaca L.) ir M.46
(P. armeniaca L.) sëklinius poskiepius, prigijimas ir augimas buvo lyginamas su kontrolinio
varianto sëkliniais poskiepiais P. cerasifera var. divaricata Borkh.
Áskiepijimo efektyvumas buvo didelis ir kito nuo 88,8% iki 97,2%, priklausomai nuo
poskiepiø ir veisliø deriniø. Vis dëlto poskiepiai neturëjo reikðmingos átakos medelyne
áskiepytø vaismedþiø skaièiui. Ið abrikosø sëkliniø poskiepiø A.4 ir M.46 iðaugo itin geros
kokybës sodinukai. Á ðiuos poskiepius áskiepyti vieneriø metø abrikosai buvo daug
aukðtesni ir tankesni uþ á P. divaricata áskiepytus vaismedþius. Abiejø veisliø abrikosø,
áskiepytø á Wangenheimo vengrinæ ir Erunosid, visi augimo rodikliai buvo menkesni negu
áskiepytø á P. divaricata.
Reikðminiai þodþiai: abrikosai, poskiepiai, veislës, augimas medelyne.
50
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 51–56.
IMPACT OF ROOTSTOCKS ON COLUMNAR APPLE
TREE GROWTH IN A NURSERY
Dalia GELVONAUSKIENË, Bronislovas GELVONAUSKIS,
Audrius SASNAUSKAS
Lithuanian Institute of Horticulture, LT-54333 Babtai, Kaunas distr.,
Lithuania. E-mail: [email protected]
There were investigated 24 columnar apple selections and 2 cultivars ‘Arbat’ and
‘Ostankino’ in a nursery at the Lithuanian Institute of Horticulture. The two latter cultivars
and selections M38-35, M38-33, M38-2, M38-15, No. 376-100 and No. 385-380 were released
in Russia and 16 hybrids (No. 23733, No. 23753, No. 24217, No. 24218, No. 24219, No.
24220, No. 24271, No. 24583, No. 24599, No. 24637, No. 24690, No. 25134, No. 26075, No.
26094 No. 26148, No. 26325) – at the Lithuanian Institute of Horticulture. Cultivars and
selections were budded on rootstocks P 60, B.396, M.26, MM.106, B.118 and ‘Antonovka’
seedlings at the height of 10–12 cm above soil and 7–10 trees were used for evaluation.
Apple trees were spaced at 0.25 x 0.9 m. Tree height and stem diameter were measured and
number of shoots were calculated in the first and second year in the nursery.
Significant differences of rootstock impact to tree height, stem diameter and shoot
number were determined. The smallest trees were on rootstocks P 60 and B.396. Apple tree
stem diameter on rootstocks B.118 and MM. 106 were the largest. The highest number of
shoots was measured on trees grown on rootstocks M.26, MM.106 and B.118. Six selections
did not raise shoots on any used rootstock.
Key words: lateral branches, rootstocks, tree height, trunk diameter.
Introduction. A columnar apple tree growth habit for the first time was described
by Lapins (1969, 1976) in Canada. The obtained results showed that this trait is
controlled by a single dominant gene, Co (Lapins, 1969, 1976). Nowadays donors of
Co gene are involved in an apple breeding programs in Russia, Latvia, Belgium,
Great Britain, USA, Bulgaria and other countries (Êè÷èíà, 1988; Drudze, 2000;
Meulenbroek et al., 1999; Tobutt, 1985; Kelsey and Brown, 1992; Djouvinov, 1994).
Donors of columnar growth habit were involved in crosses at the Lithuanian Institute
of Horticulture in 1988.
It was determined that tree height, trunk diameter, number of shoots and other
tree characteristics depend on rootstock (Inomata et al., 2003, 2005). Rootstocks
influence apple tree productivity, fruit weight and firmness (Lauri and Lespinasse,
1993; Lauri, et al., 1995; Kvilys, 2002; Inomata et al., 2003, 2005). Results obtained
by researchers in France and Japan showed that apple trees with common habitus
are more productive and biennial bearing is not so evident than it is typical for trees
with columnar type habitus.
51
Materials and methods. There were investigated 24 advanced selections and 2
columnar-type apple cultivars ‘Arbat’ and ‘Ostankino’ at nursery of the Lithuanian
Institute of Horticulture. Latter two cultivars and selections M38-35, M38-33,
M38-2, M38-15, No. 376-100 and No. 385-380 were received in Russia and the rest
16 selections (No. 23733, No. 23753, No. 24217, No. 24218, No. 24219, No. 24220,
No. 24271, No. 24583, No. 24599, No. 24637, No. 24690, No. 25134, No. 26075,
No. 26094, No. 26148, No. 26325) were received at the Lithuanian Institute of
Horticulture. ‘Arbat’ was used as a donor of columnar growth habit. Columnar apple
cultivars and selections were grafted on rootstocks P 60, B.396, M.26, MM.106,
B.118 and Antonovka seedlings. Trees were planted at the spacing of 25 x 90 cm in a
nursery. There were evaluated 7–10 plants per cultivar or selection in the nursery. Tree
height, trunk diameter and shoot (length more than 3 cm) number was evaluated in the
first and second year of tree growth. Trees were fertilized and sprayed with pesticides
according to the technology applied at the Lithuanian Institute of Horticulture.
Results. Average height of trees of 26 apple cultivars and selections on different
rootstocks varied from 66 cm to 76 cm at the end of the first year (Fig.). The
highest trees were on rootstocks ‘Antonovka’ seedlings and B.118. Trees were
significantly lower on rootstocks B.396 and P 60 than it was measured on previous
two rootstocks. Two years old apple trees grafted on ‘Antonovka’ seedlings were
significantly higher than on trees grafted on dwarf rootstocks. The lowest trees
were on rootstocks B.396 and P 60.
F i g. Impact of different rootstocks on average tree height of 26 apple cultivars and
selections
P a v.
Ávairiø poskiepiø átaka 26 koloniniø obelø veisliø ir selekciniø numeriø medeliø
vidutiniam aukðèiui
PA – ‘Antonovka’ seedlings / PA – ‘Paprastojo antaninio’ sëjinukai.
Tree height, trunk diameter and shoot number of apple cultivars and selections
trees with columnar type habit on six rootstocks is presented in Table 1. Significant
52
differences were estimated between cultivars and selections for above noted traits.
The height of two-year-old trees of eight selections was 100 cm or less. It varied
from 88 cm to 100 cm.
T a b l e 1. Mean value of traits of apple cultivars and selection trees
on six rootstocks
1
l e n t e l ë. Obelø veisliø ir selekciniø numeriø sodinukø, augintø su ðeðiais
poskiepiais, vidutiniai augimo rodikliai
Cultivar
Veislë, selekcinis numeris
Height / Aukštis, cm
Trunk diameter
Shoot number
Kamieno skersmuo, mm
Ðakø skaièius
2000
2001
2001
2001
M38-35
57
88
11
0.6
No. 0833
59
90
11
1
No. 24220
49
93
12
0
M38-33
51
93
12
0
No. 24583
61
94
12
0
No. 0749
52
96
13
0
M38-2
62
96
10
1.4
M38-15
52
100
11
0
‘Ostankino’
72
112
12
0.3
No. 24271
56
115
12
0
No. 376-100
59
117
12
3.5
No. 385-380
71
122
12
0.1
No. 24599
69
125
12
0.3
No. 26148
64
126
11
0.7
No. 25134
79
139
12
1.8
No. 24637
74
143
11
1.2
‘Arbat’
67
147
12
1
No. 24218
73
147
13
0.2
No. 24217
83
151
10
1.4
No. 26325
87
151
11
2.4
No. 24690
83
156
11
0.9
No. 26075
88
162
11
4.8
No. 24219
84
176
11
1.9
No. 23733
99
178
10
0.9
No. 23753
103
181
11
1.2
No. 26094
98
187
12
1.2
LSD05 / R05
18.2
31.7
0.8
1.1
53
The average tree height of 8 selections was higher than 150 cm and varied from
151 cm to 187 cm. Trunk diameter of cultivars and most selections was 11–12 mm.
The highest diameter (13 mm) was detected for No. 0749 and No. 24218, the lowest
(10 mm) – for M38-2, No. 24217 and No. 23733. The highest trunk diameter of
trees of investigated cultivars and selections was determined on rootstocks B.118
and MM.106, 13 mm and 12 mm, respectively (Table 2). The average shoot number
per tree depends on genotype, because 6 selections grafted on Antonovka seedlings
and 5 dwarf rootstocks did not have shoots (Table 1). Other selections and two
cultivars grew shoots and its number varied from 0.1 to 4.8. The significantly highest
shoot number was calculated for selections No. 26075 (4.8) and No. 376-100 (3.5).
On the other hand, shoot number was influenced by rootstock as well (Table 2).
Apple cultivars and selections had the highest shoot number (1.8) on rootstock M
26. The lowest shoot number (0.4) was estimated on apple trees grafted on rootstock
B.396.
T a b l e 2. Impact of rootstocks on mean value of traits of apple
cultivars and selection trees
2
l e n t e l ë.
Poskiepio átaka obelø veisliø ir selekciniø numeriø sodinukø
vidutiniams augimo rodikliams 2001 m.
Trait / Požymis
Trunk diameter / Kamieno
Rootstock / Poskiepis
LSD05 / R05
PA*
B.118
MM.106
M.26
B.396
P 60
11
13
12
11
11
11
0,8
0,7
1,4
1,4
1,8
0,4
0,6
0,6
skersmuo, mm
Shoot number / Ðakø skaièius
* ‘Antonovka ’ seedlings / ‘Paprastojo antaninio’ sëjinukai
Discussion. Two-year-old apple trees height on dwarf rootstocks B.396 and
P 60 were 30% lower than it was estimated for trees grafted on Antonovka seedlings.
Differences of one-year-old trees grafted on above mentioned rootstocks were about
15%. Our results and results of Chinese researches (Dai Hong Yi et al., 1998) shows
that dwarf rootstocks are efficient tool to control the height and shoot number of
columnar type apple trees. The average height of smallest selections of two-year-old
columnar apple trees on six rootstocks was 2.1 times lower than it was measured
for strong grown selections (Table 2). Our results show that height of columnar
type apple trees is influenced by rootstock. Trunk diameter is influenced by rootstock
as well. The part of investigated selections did not develop shoots and used rootstocks
did not influence expression of this trait. A tendency of dwarf cultivars or selections
to have low number of shoots was emphasized (Table 1). It is shown by other
researches that apple tree height and columnar type trees as well and shoot number
is determined genetically (Decourtye, 1967; De Wit et al., 2004; Kenis and Keulemans,
2004).
Conclusions. 1. Rootstocks influence the growth and trunk diameter of columnar
type apple trees. The highest apple trees were recorded on rootstock Antonovka
seedlings and the highest trunk diameter – on rootstocks B.118 and MM.106.
54
2. Shoots were not detected on trees of six selections (M38-33, M38-15, No.
24220, No. 24583, No. 24271, No. 0749) grafted on five dwarf rootstocks and
Antonovka seedlings. The highest number of shoots was estimated for trees grafted
on rootstocks M.26, MM.106 and B.118.
Gauta
2006 07 04
Parengta spausdinti
2006 07 31
References
1. D a i H. Y., W a n g S. G., Y u S. M., W a n g R. Y u X. M. Study
on the performance of columnar apple varieties // Journal of fruit science. 1998. 15(1): 13–19.
2. D d j o u v i n o v V. Apple and pear breeding in Bulgaria. In Schmidt H.,
Kellerhals M. (eds) Progress in temperate fruit breeding, Kulwer Academic publishers.
1994. P. 127–129.
3. D e c o u e t y e L. Etude de quelques caracteres a controle genetique simple
chez le pommier (Malus sp.) et le poirier (Pyrus communis) // Ann.Amelior.Plantes. 1967.
17(3):243–266.
4. D e W i t I., C o o k N. C., K e u l e m a n s J. Characterization of tree
architecture in two-year-old apple seedlings populations of different progenies with a
common columnar gene parent // Acta horticulturae. 2004. 663: 363–368.
5. D r u d z e I. Studies on perspective apple and pear hybrids of breeding station
“Iedzeni” in Latvia // Acta Horticulturae. 2000. 538: 729–734.
6. I n o m a t a Y., K u d o K., M a s u d a T., B e s s h o H., W a d a
M. and S u z u k i K. Growth and fruit productivity habits of columnar type apple
selections // Horticultural research (Japan). 2004. 3(4): 392–401.
7. I n o m a t a Y., K u d o K., W a d a M., M a s u d a T., B e s s h o
H., S u z u k i K. The influence of rootstock on characteristics of tree growth, fruit
productivity and dry matter production of ‘Maypole’ young apple tree // Horticultural
research (Japan). 2005. 4(1): 41–46.
8. K e l s e y D. F. and B r o w n S. K. ‘McIntosh Wijcik’: A columnar mutation
of ‘McIntosh’ apple proving useful in physiology and Breeding Research // Fruit Var. J.
1992. 46: 83–87.
9. K e n i s K., K e u l e m a n s J. QTL analysis of growth characteristics in
apple // Acta horticulturae. 2004. 663: 369–374.
10. K v i k l y s D. Apple rootstock research in Lithuania with aspect to quality
and tree productivity // Horticulture and vegetable growing. 2002. 21(3): 3–13.
11. L a p i n s K. O. Segregation of compact growth types in certain apple seedling
progenies // Can. J. Plant Sci. 1969. 49: 765–768.
12. L a p i n s K. O. Inheritance of compact growth type in apple // J. Amer. Soc.
Hort. Sci. 1976. 101: 133–135.
13. L a u r i P. E., T e r o u a n n e E., L e s p i n a s s e J. M.,
R e g n a r d J. L. and K e l n e r J. J. Genotype differences in the axillary bud
growth and fruiting pattern of apple fruiting branches over several years – an approach to
regulation of fruit bearing // Scientia Horticulturae. 1995. 64: 265–281.
55
14. L a u r i P. E., L e s p i n a s s e J. M. The relationship between cultivar
fruiting type and Fruiting branch characteristics in apple trees // Acta Horticulturae. 1993.
349: 259–263.
15. M e u l e n b r o e k B., V e r h a e g h J. and J a n s e J. Inheritance
studies with columnar type trees // Acta Horticulturae. 1999. 484: 255–258.
16. T o b u t t K. R. Breeding columnar apple at East Malling // Acta Horticulturae.
1985. 159: 63–68.
17. Ê è ÷ è í à Â. Â.
Ñàäû êîëëîííûõ ôîðì ÿáëîíè // Ñàäîâîäñòâî
è âèíîãðàäaðñòâî. 1997. 1: 22–24.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 51–56.
POSKIEPIØ ÁTAKA KOLONINIØ OBELØ SODINUKØ AUGUMUI MEDELYNE
D. Gelvonauskienë, B. Gelvonauskis, A. Sasnauskas
Santrauka
Lietuvos sodininkystës ir darþininkystës instituto medelyne tirti 24 selekciniai numeriai
ir 2 koloninio tipo obelø veislës – ‘Arbat‘ ir ‘Ostankino‘. Pastarosios veislës ir selekciniai
numeriai M38-35, M38-33, M38-2, M38-15, Nr. 376-100 ir Nr. 385-380 sukurti Rusijoje, 16
kitø selekciniø numeriø (Nr. 23733, Nr. 23753, Nr. 24217, Nr. 24218, Nr. 24219, Nr. 24220,
Nr. 24271, Nr. 24583, Nr. 24599, Nr.2 4637, Nr. 24690, Nr. 25134, Nr. 26075, Nr. 26094 Nr. 26148,
Nr. 26325) sukurta Lietuvos sodininkystës ir darþininkystës institute. Kuriant pastaruosius
hibridus, kaip tëvinë forma panaudota ’Arbat‘ veislë, kuri yra koloninës vaismedþiø formos
donorë. Buvo tirta po 7–10 medeliø, áakiuotø á poskiepius P 60, B.396, M.26, MM.106,
B.118 ir Paprastojo antaninio sëjinukus 10–12 cm aukðtyje. Medeliai auginti 0,25 x 0,9 m
atstumais. Pirmaisiais ir antraisiais augimo medelyne metais matuotas augalø aukðtis ir
kamieno skersmuo ir suskaièiuotos ðakos.
Nustatyta, kad poskiepiai ið esmës veikë koloniniø obelø veisliø ir selekciniø numeriø
sodinukø aukðtá, kamieno skersmená ir ðoniniø ðakø skaièiø. Þemiausi buvo sodinukai su
P 60 ir B.396 poskiepiais, storiausi – su B.118 ir MM.106 poskiepiais. Daugiausia ðakø
iðaugino sodinukai su poskiepiais M. 26, MM.106 ir B.118. Ið tirtø 2 veisliø ir 24 selekciniø
numeriø 6 selekciniø numeriø vaismedþiai ðoniniø ðakø neiðaugino në su vienu poskiepiu.
Reikðminiai þodþiai: ðoninës ðakos, poskiepiai, vaismedþiai, aukðtis, kamieno
skersmuo.
56
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 57–61.
QUALITY OF MAIDEN APRICOT TREES DEPENDING ON
ROOTSTOCK AND CULTIVAR
Maria LICZNAR-MAÙAÑCZUK, Ireneusz SOSNA
Department of Horticulture, University of Agriculture, Rozbrat 7, 50-334
Wrocùaw, Poland. E-mail: [email protected]
The experiment was established at Fruit Experimental Station near Wrocùaw. Three
apricot cultivars – ‘Harcot’, ‘Hargrand’ and ‘Bergeron’ – were budded on three rootstocks:
seedlings Somo and clone LS-4 seedlings (P. armeniaca) and Pumiselect®. The aim of the
investigation was to evaluate the quality of maiden apricot trees depending on rootstock
and cultivar.
In the autumn of 2005 the thickest trunks in the nursery had apricot trees ‘Harcot’,
while apricot trees ‘Hargrand’ were the best feathered. Clearly the weakest growth was
noted of ‘Bergeron’. Irrespective of cultivars, apricot trees budded on Pumiselect®
rootstock were characterised of the strongest vigour. Maidens budded on seedlings Somo
grew similarly to LS-4 seedlings but more often weaker. Irrespectively of cultivars, the
longer root system had all trees on the generative rootstocks – Somo and clone LS-4
seedlings (45–50 cm). The average length of the rooted rootstock Pumiselect® was only
13.4 cm. Number of scaffold and lateral roots was also similar for both generative rootstocks.
Cvs. ‘Hargrand’ and ‘Harcot’ on seedlings Somo were characterised by the best quality of
root system, whereas ‘Bergeron’ irrespective of rootstocks was the worst rooted.
Key words: apricot, rootstock, cultivar, maiden, root system, Pumiselect.
Introduction. In the case of many apricot cultivars, reduction of growth is
only possible by using a proper rootstock (Grzyb el al., 1996; Szalay and Molnár,
2004). Rootstock not only influences the growth vigour, but also can affect the
lifespan of trees (Dimitrova, 2001). Properties of rootstocks have been evaluated as
a part of research and breading programs at the experimental stations (Vachùn et al.,
1995; Dimitrova, 2002).
Several good rootstocks from Prunus cerasifera, Prunus domestica, Prunus
insititia and also Prunus persica have been introduced in cultivation of apricot (Bassi,
2001; Jakubowski, 2004). None of them is widely distributed and well adapted to
the different soil environment. A full compatibility of rootstock with all cultivars is
not found yet (Bassi, 2001). Dimitrova and Marinov (2002) had no signal of grafting
incompatibility on the Myrobalan seedlings during 30 years of research work in
Bulgaria. In Poland, Grzyb et al. (1996) observed the highest percentage of dead
57
trees grafted on Wangenheim Prune, but seedling Somo 86 was recognised as a
good rootstock for all investigated cultivars except ‘Harcot’. Licznar-Maùañczuk
and Sosna (2005b) observed grafting incompatibility of cv. ‘Morden 604’ and
rootstock Somo.
Apricot trees ‘Harcot’, ‘Hargrand’ and ‘Bergeron’ were recognised as good
cultivars to the climatic conditions of the Lower Silesia region (Licznar-Maùañczuk
and Sosna, 2005 a; 2005b). The aim of the present studies was the estimation of
quality of one-year-old apricot trees of these cultivars depending on rootstock use.
Materials and methods. In 2004–2005, the experiment was conducted at Fruit
Experimental Station, which belong to the Agricultural University of Wrocùaw (southeast of Poland). Three apricot cultivars: ‘Harcot’, ‘Hargrand’ and ‘Bergeron’ were
budded on three rootstocks: seedlings Pumiselect®, Somo and clone LS-4 seedlings.
Pumiselect® (Rhenus 2) as a clonal Pumiselect pumila rootstocks for peach
and apricot, was propagated by hardwood cuttings. In the autumn of 2003 oneyear-old hardwood shoots were pruned at 40 cm long sections. During winter they
were kept in box with wet peat in room with about 3oC and in the spring of 2004
were planted to the nursery in the depth of 20 cm. The seeds of Polish apricot
cultivar ‘Somo’ and Polish apricot clone LS-4 (both comes from Prunus armeniaca)
were stratificated and sown in the spring of 2004. In the summer of 2004 each
rootstock was budded.
In the autumn of 2005, the number of obtained trees varied from 13 to 33
among nine of experimental combination. The apricot estimation was based on 16
selected trees, except cv. ‘Bergeron’ on rootstock Pumiselect® (only 12 trees).
Quality of each selected one-year-old tree was evaluated in the autumn of 2005. The
length of the rooted stock for vegetative rootstock Pumiselect® was measured and
the total number of the main roots were counted. Number of scaffold and lateral
roots was counted for both generative rootstocks, and the length of root system
was also measured. Trunk and rootstock cross-section area was calculated basing
on diameter measured 30 cm above and just below the place of budding, respectively.
In addition, the length of annual shoots for one of the average chosen tree from
every replication was measured.
The experiment was evaluated separately for each cultivar, as a completely
randomised design with four replications, including four or three trees. Experimental
data were statistically elaborated and verified by Student’s multiple range t-test at
P = 0.05.
Results and discussion. In the autumn of 2005 maiden apricot trees,
irrespectively of rootstock, looked healthy. There were noted some dead trees caused
by Bacterial canker, but did not observed incompatibility symptoms in the nursery.
It was very promising, because according to Bassi (2001), even the use P. armeniaca
selections as a rootstock, could lead to incompatibility in some cultivars.
In this experiment the quality of maiden apricot trees depended on cultivar and
rootstocks. The thickest trunks had apricot trees ‘Harcot’, while apricot trees
‘Hargrand’ were the best feathered (Table 1). Clearly the weakest growth in the
nursery was noted of ‘Bergeron’. These results are similar to those reported by
Lopez and Brunton (2000). The estimated rootstocks had significant influence mainly
58
on total length of laterals (with the exception of ‘Bergeron’). Irrespective of cultivars,
apricot trees budded on rootstock Pumiselect® were characterised by the strongest
vigour. In some cases, even significant differences were noted. This vegetative
rootstock had the biggest cross section area, as well. It is interesting, because
Pumiselect® is taken for dwarf rootstock. Maidens budded on seedlings Somo grew
similarly to LS-4 seedlings or more often weaker. This contradicts to the studies by
Grzyb et al. (1996), who did note clearly retarding of vegetative growth of trees on
seedlings Somo 86 in comparison to strongly growing seedlings Myrobalan
(P. cerasifera). However, in studies of Dimitrova and Marinov (2002), trees grafted
on apricot seedlings grew much weaker than those on seedlings Myrobalan.
T a b l e 1. Characteristic of maiden apricot trees depending on
rootstock
1
l e n t e l ë. Poskiepiø átaka abrikosø sodinukø kokybei
Cultivar / Rootstock
Veislë / Poskiepis
Rootstock cross Trunk cross Number of annual
Total lengthof
section area section area
shoots
annual shoots
Poskiepio
skerspjûvio plotas,
cm
‘Bergeron’
2
< 20 cm
> 20 cm
Bendras ðakø
ilgis, cm
3.97
0.95
5.8
6.3
366.9
2.79
0.90
6.0
6.5
359.9
Seedling Somo
2.79
0.82
5.5
6.5
359.9
3.18
0.89
5.8
6.4
362.2
0.43
NS
NS
NS
LS-4 sëklinis poskiepis
LSD05 / R05
Pumiselect®
6.13
1.65
9.8
10.8
654.1
LS-4 seedling
3.38
1.19
3.8
7.5
422.8
seedling Somo
3.25
1.02
3.8
7.0
364.1
8.4
NS
480.3
LS-4 sëklinis poskiepis
Somo sëklinis poskiepis
X
4.25
1.29
5.8
Pumiselect®
5.47
0.56
1.27
0.39
18.0
15.3
2.7
829.9
LS-4 seedling
2.92
0.88
14.8
8.0
466.6
seedling Somo
3.34
1.16
14.0
7.3
446.6
3.91
1.10
15.6
NS
10.2
NS
581.0
LSD05 / R05
‘Hargrand’
Ðakø skaièius
Pumiselect®
LS-4 seedling
Somo sëklinis poskiepis
X
‘Harcot’
Kamieno
skerspjûvio
2
plotas, cm
LS-4 sëklinis poskiepis
Somo sëklinis poskiepis
X
0.52
LSD05 / R05
2.8
Irrespectively of cultivar, apricot trees had the longer root system on the
generative rootstocks – Somo and clone LS-4 seedlings (Table 2). Well-developed
and strong root system is typical for generative rootstocks. Such root system causes
that trees grafted on apricot seedlings (P. armeniaca) requires less water and they
are more tolerant to drought than apricot trees on rootstock P. domestica or
59
P. insititia (Szalay and Molnár, 2004). The average length of the rooted stock for
vegetative Pumiselect® was only 13.4 cm. Number of scaffold and lateral roots was
also similar for both generative rootstocks. Irrespective of rootstocks, ‘Hargrand’
and ‘Harcot’ cvs. on seedlings Somo were characterised by the best quality of root
system, whereas ‘Bergeron’ rooted the worst.
T a b l e 2. Characteristic of maiden apricot trees root system
depending on rootstock
2
l e n t e l ë.
Poskiepiø átaka abrikosø sodinukø ðaknø sistemai
Cultivar / Rootstock
Veislë / Poskiepis
Pumiselect®
LS-4 seedling
Length of Length of
rooted stock
root
Total
Number of
Number of
number of
scaffold
lateral roots
Ásiðaknijusio
roots
roots
Šaknies ilgis,
Ðoniniø ðaknø
poskiepio
Skeletiniø
Bendras ðaknø
skaièius
cm
dalis, cm
ðaknø skaièius
skaièius
15.7
11.9
-
44.3
3.0
6.7
9.7
-
44.3
2.8
4.5
7.2
-
44.3
-
2.9
NS
5.6
NS
9.6
1.6
Pumiselect®
11.3
-
-
-
11.9
LS-4 seedling
-
52.0
3.1
11.9
15.0
seedling Somo
-
55.8
2.6
15.7
18.2
-
53.9
-
2.9
NS
13.8
NS
15.1
‘Bergeron’ LS-4 sëklinis poskiepis
Seedling Somo
Somo sëklinis poskiepis
X
LSD05 / R05
‘Harcot’
LS-4 sëklinis poskiepis
Somo sëklinis poskiepis
X
LSD05 / R05
Pumiselect®
LS-4 seedling
‘Hargrand’
LS-4 sëklinis poskiepis
seedling ‘Somo
Somo sëklinis poskiepis
X
LSD05 / R05
2.1
13.2
-
-
-
-
14.7
40.2
4.1
11.3
15.4
-
52.4
3.5
12.8
16.3
-
46.3
-
3.8
12.1
NS
15.5
NS
6.0
Conclusions. 1. Quality of maiden apricot trees depended on cultivar and
rootstocks. Clearly the weakest growth in the nursery was noted of ‘Bergeron’.
Apricot trees budded on rootstock Pumiselect® grew much stronger in comparison
to seedlings P. armeniaca.
2. Irrespectively of cultivar, apricot trees budded on seedlings P. armeniaca
were better rooted than those on rootstock Pumiselect®.
Gauta
2006 05 04
Parengta spausdinti
2006 07 18
60
References
1. B a s s i D. Apricot culture: present and future. In: I Karayiannis (ed.), XI Int.
Symp. on Apricot Culture, ISHS 1999 // Acta Horticulturae. 2001. Vol. 488. P. 35–40.
2. D i m i t r o v a M. The influence of rootstock on the growth and productivity of
tree apricot cultivars // Bulgarian Journal of Agricultural Science. 2001. Vol. 7. P. 161–166.
3. D i m i t r o v a M. Evaluation of some plum rootstocks as rootstock for apricot
in the orchard // Acta Horticulturae. 2002. Vol. 577. P. 311–314.
4. D i m i t r o v a M., M a r i n o v P. Myrobalan (P. cerasifera Ehrh.) as
a rootstock for apricot // Acta Horticulturae. 2002. Vol. 577. P. 315–318.
5. G r z y b Z., Z d y b H., S i t a r e k M. Wpùyw róýnych podkùadek na
zdrowotnoúã siùæ wzrostu i owocowanie moreli // Zeszyty Naukowe ISiK - Skierniewice.
1996. Vol. 3. P. 55–62.
6. J a k u b o w s k i T. Uprawa moreli. Hortpress. Sp. z o.o. Warszawa, 2004. 160 p.
7. L i c z n a r - M a ù a ñ c z u k M., S o s n a I. Evaluation of several apricot
cultivars and clones in the Lower Silesia conditions. Part I: Blossoming of trees, yield and
fruit quality // Journal of Fruit and Ornamental Plant Research. 2005a. Vol. 13. P. 39–48.
8. L i c z n a r - M a ù a ñ c z u k M., S o s n a I. Evaluation of several apricot
cultivars and clones in the Lower Silesia conditions. Part II: Vigour, health and mortality /
/ Journal of Fruit and Ornamental Plant Research. 2005b. Vol. 13. P. 49–57.
9. L o p e z G. P., B r u n t o n G. J. Comportamiento de variedades de
albaricoquero en la comarca del noroeste de la Region de Murcia // Jornadas de
experimentacion en fruticultura. 2000. Vol. 21. P. 163–170.
10. S z a l a y L., M o l n á r B. P. The effect of rootstock on tree size of
apricot cultivars // International Journal of Horticultural Science. 2004. Vol. 10(3). P. 57–58.
11. V a c h ù n Z., K r ð k a B., S a s k o v á H. Results of apricot research
and breeding programme at the Horticultural Faculty in Lednice na Morawie // Zahradnictvi.
1995. Vol. 22(3). P. 95–98.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 57–61.
POSKIEPIO ÁTAKA SKIRTINGØ VEISLIØ ABRIKOSØ SODINUKØ
KOKYBEI
M. Licznar-Maùañczuk, I. Sosna
Santrauka
Bandymas atliktas Sodininkystës tyrimø stotyje netoli Vroclavo. Trys abrikosø veislës:
‘Harcot’, ‘Hargrand’ ir ‘Bergeron’, buvo áskiepytos á Somo ir LS-4 (P. armeniaca) sëklinius
poskiepius ir Pumiselect® vegetatyviná poskiepá. Tyrimo tikslas – ávertinti poskiepio átakà
abrikosø sodinukø kokybei. 2005 m. rudená medelyne storiausi buvo ‘Harcot’ veislës
sodinukø kamienai. Ðios veislës sodinukai labiausiai ðakojosi. Prasèiausiai augo ‘Bergeron’
veislës abrikosai. Visø veisliø abrikosai su Pumiselect® poskiepiu augo geriausiai. Á Somo
sëklinius poskiepius áskiepytos abrikosø veislës augo beveik taip pat, kaip áskiepytos á
LS-4, bet daþnai ir prasèiau. Ilgesnes ðaknis (45–50 cm) iðleido visø veisliø su Somo ir
LS-4 sëkliniais poskiepiais sodinukai, o sodinukø su Pumiselect® ðaknø ilgis buvo tik
13,4 cm. ‘Hargrand’ ir ‘Harcot’ veisliø abrikosø sodinukø su Somo poskiepiu ðaknø sistema
buvo geriausios kokybës. ‘Bergeron’ veislës sodinukø su visais poskiepiais ðaknø sistema
buvo prasèiausia.
Reikðminiai þodþiai: abrikosai, poskiepiai, veislës, sodinukai, ðaknø sistema,
Pumiselect.
61
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 62–70.
THE INFLUENCE OF ION EXCHANGE SUBSTRATES
(BIONA-112 AND BIONA-312) ON BIOCHEMICAL
PARAMETERS OF PRUNUS L. ROOTSTOCKS DURING
ADAPTATION EX VITRO
Tatjana KRASINSKAYA, Natalija KUKHARCHYK
Institute for Fruit Growing of the National Academy of Sciences of Belarus,
2 Kovalev str., Samokhvalovichy, Minsk reg., 223013 Belarus.
E-mail: [email protected]
It is known that the plant reorganization after in vitro culture is performed not only
in morphological but also in physiological direction during the adaptation ex vitro.
Different methods are applied for improving of adaptation stage. One of them is
using of ionic soils as adaptation substrates. As a result of that, the aim of our investigations
was to study plant physiological development on Prunus L. rootstocks, for example,
VSL-2 (Prunus fruticosa (Pall.) G. Waron. x P. lannesiana Carr.) and OVP-2 (P. cerasus
x P. Maackii) on ion-exchange substrates (IES) with different mineral compositions
(BIONA-112 and BIONA-312) at the adaptation to aseptic conditions ex vitro.
Evaluation of plant physiological development was made according to these
biochemical indices: chlorophyll (a + b) content (mg/dm2), sugar concentration (glucose +
saccharose) (%) and dry weight (%).
Significant influence of IES on chlorophyll, sugar and dry weight accumulation were
established as a result of our investigation. The significant positive after-effect of ionexchange adaptation substrates on plant physiological development was marked at the
second stage of adaptation.
Key words: Prunus L., ion exchange substrate, BIONA-112, BIONA-312, biochemical
parameters, chlorophyll, soluble sugars, dry matter content, ex vitro, adaptation, Belarus.
Introduction. Plants during ex vitro adaptation undergo certain changes in both
morphological and physiological aspects. First of all, the plants launch from
heterotrophic to autotrophic kind of nutrition because of the resumption of their
photosynthetic activity. Secondly, transpiration changes take place to promote the
adaptation of the plants to low moisture level, which is typical for their traditional
conditions of growing (the transpiration becomes controlled, the majority of stoma
close and comes to the inner parts of the leave tissue (Vegvari, Vertesy, 1999), cuticle
and epicuticle wax layer develop more intensively then in test-tube plants, the chemical
compound of wax changes (Ãèãîëîøâèëè, 2000)).
Different methods are used to accelerate and improve the adaptation stage, with
the aim to increase the number of normally adapted plants in ex vitro: the reduction
62
of nitrates concentration in nutrient medium for micro breeding, the using of waxes
for splashing the leaves after in vitro and others (McClelland et al., 1990). One of
the methods developed to improve plant adaptation is the usage of qualitative new
adaptation substrates, for example, ion exchange substrates (ionite soils). There are
known the advantages of ion exchange substrate using for growing fruits and small
fruits and ornamental plants (Ñâiðø÷ý¢ñêàÿ et al., 1995; Ñîëäàòîâ et al.,
1978; Ñóäåéíàÿ, Òèìîôååâà, 2003; Ñóäåéíàÿ, Óòûðî, 2000; Òóëàåâà
et al., 1990) for the in vitro rooting microshoots of potatoes after in vitro
(Ìàòóñåâè÷ et al., 1995), and for adaptation ex vitro of Prunus L. regenerates.
In previous researches we determined the statistically significant influence of
the substrates on the morphological development of plant Prunus L. To determine
the causes of considerable difference between the intensity of ontogenesis of
regenerates adapted on different substrates, in this work we study their influence on
physiological and biochemical processes, which occur in plant during ex vitro stage.
Materials and methods. The researches were carried out in the department of
biotechnology at the Institute for Fruit Growing of the National Academy of Sciences
of Belarus during 23.06.2004 – 7.04. 2005. Objects of research were peat substrate
(control), ion exchange substrates (BIONA-112 and BIONA-312); vegetative
rootstocks of sour cherry and sweet cherry – OVP-2 (Prunus cerasus x P. Maackii).
VSL-2 (P. fruticosa (Pall.) G. Waron. x P. lannesiana Carr.).
Peat substrate represents a mixture of substrate „Florabel-5” and river sand in
ratio 3 : 1, autoclaved under the pressure of 1.2 atmospheres during 2 hours. The
structure of water extract obtained after the autoclaving of peat substrate is represented
in Table 1. The pH value of water extract from peat substrate is 7.7.
This substrate was used also on the second stage of adaptation.
T a b l e 1. Ionic composition of substrates
1
l e n t e l ë.
Joninë terpiø sudëtis
Concentration of ion / Jonø koncentracija, mg-eqv/l
Substrate
Terpë
Ê
Ñà2+
H2P04– SÎ42–
Mg2+
Fe3+
NH4+
N03–
PEAT substrate 0.697 0.48 3.20
2.8
0.122
0.37
1.28
0
1.254
1.76
BIONA-112
BIONA-312
2.93
0.9
0.10
-
2.61
0.21
11.43
8.6
1.02
0.42
2.43
0.87
1.72
0.08
+
+
Na
Durpiø substratas
6.86 1.57
2.9 2.3
4.4
3.7
Cl–
The substrate of BIONA-112 is ion exchange substrate created on the basis of
cation exchanger KU-2 (H+) and anion exchanger EDE-10P (Î͔) in ratio 1 : 2.05. It
was rich by various macro- and microelements in the ion exchange form (Table 1).
The pH value of water extract from substrate BIONA 112–6.05.
The substrate BIONA-312 is the mixture of ion exchange substrate BIONA-112
(56 percent by weight) with cliniptilolite. The pH value of water substrate
BIONA-312 is 6.5–6.7.
The adaptation was carried out in 2 stages. Stage I (the adaptation stage). The
63
plants after the in vitro rhizogenesis stage were planted into 50 ml holders filled with
peat or ion exchange substrates, covered with plastic film in order to increase moisture.
Watering was performed with distilled water. The adaptation of the plants was fulfilled
in the third quarter of 2004. On the stage II (post-adaptation stage) the plants were
transplanted into 500 ml pots filled with peat substrate. The conditions of adaptation
on the first and second stages: illumination 2.5–3.0 th. Lux, temperature 20–22°C,
photoperiod 16/8 hours. The length of each stage was 17 weeks.
The influence and post-influence of adaptation substrates on the physiological
development of the plants was analyzed according to the data of biochemical analyses
of the leaves in 4 replications: the chlorophylls a and b content (Åðìàêîâ, 1987);
the soluble sugars content (monosugars (glucose + fructose) + saccharose)
(Êàðìàíåíêî, Êàçàíöåâà, 1986); dry matter content (Åðìàêîâ,1987).
The results were analyzed statistically by ANOVA and the significance of
differences between means was evaluated by Duncan’s multiple range test at
P = 0.05 with the help of Statistica 6.0 software. Results were represented in Tables
and included the mean±SE. Significance of differences in Tables is shown at
p< 0.05 (a), p< 0.01 (b), p < 0.001 (c), non-significant (–).
Result and discussion. C h l o r o p h y l l c o n t e n t. The factual influence
of the substrates on the accumulation of photosynthetic pigments in the unit of the
leaves area was marked. All the parameters characterizing the accumulation of
pigments in the leaves during their adaptation on any ion exchange substrate not
depending on its content, was lower than on the peat substrate (Table 2).
In the investigated rootstocks the accumulation of the chlorophylls was different
and depended on the genotype. The maximum level of Chl b synthesis was marked
for the rootstock OVP-2 on the peat substrate, the minimum data by this rootstock
– on the substrate BIONA-312. The synthesis of Chl b by the rootstock VSL-2 was
even and did not depend on the adaptation substrate.
The Chl ratio a/b was the highest in rootstocks OVP-2. Depending on the
adaptation substrate this data positively did not change by any of both rootstocks.
S o l u b l e s u g a r s. Intensive accumulation of sugars was observed in
plants adapted on the peat substrate and substrate BIONA-312 (Table 2). This
tendency is obviously manifested during the adaptation of the rootstock OVP-2. The
synthesis of monosugars in the leaves certainly did not differ on different adaptation
substrates. More saccharose was accumulated in the plants, adapted on the peat
substrate.
Dry matter content. According to literature data, ion exchange substrate promotes
the accumulation of water in the leaves of the plants, so it is advisable to use it when
growing for leave product (Áàõíîâà ir kt., 1999). We have investigated the certain
decrease of dry matter content while the adaptation of regenerates of sour cherry on
the substrate BIONA-112; simultaneously, the essential increase in the volume of the
above-ground plant organs was shown. The quantity of dry matter content on the
substrate BIONA-312 was higher than on the substrate BIONA-112, but slightly
lower than at peat substrates. The maximum amplitude in the accumulation of dry
matter content on different substrates was marked for rootstock OVP-2: the leaves
of the regenerates adapted on the peat substrate, contained the maximum dry matter
quantity.
64
T a b l e 2. Biochemical parameters characterizing physiological
development of rootstocks at the adaptation stage, n = 4
2
l e n t e l ë. Biocheminiai rodikliai, charakterizuojantys fiziologiná poskiepiø
vystymàsi adaptacijos etape, n = 4
Adaptation substrates (factor Â)
Forms of
rootstocks
(factor A)
Poskiepiø
formos (A
faktorius)
Adaptacijos terpës (B faktorius)
Biochemical
parameters
Biocheminiai rodikliai
Stem length
ñm
Chl à, mg/dm2
Chl b, mg/dm2
Ñhl à+b, mg/dm2
Chl à/b, mg/dm2
Monosugars
Monocukrûs, %
OVP-2 Saccharose /
Sacharozë, %
Sugar concentration
Stiebo ilgis,
Cukraus koncentracija,
%
Dry matter content
Sausøjø medþiagø
kiekis, %
Stem length
ñm
Chl à, mg/dm2
Chl b, mg/dm2
Ñhl à+b, mg/dm2
Chl à/b, mg/dm2
Monosugars
Monocukrûs, %
VSL-2 Saccharose
Sacharozë, %
Sugar concentration
Cukraus koncentracija,
%
Dry matter content
Stiebo ilgis,
Sausøjø medþiagø kiekis,
BIONA-112
BIONA-312
A faktoriaus
vidurkis
3.9 ± 0.23
6.7±0.44 –
5.5 ± 0.28 – –
5.4 ± 0.38
3.03 ± 0.20
1.16 ± 0.14
4.19 ± 0.33
2.66 ± 0.16
2.64±0.14 –
1.12±0.14 –
3.51±0.37 –
2.50±0.45 –
2.49 ± 0.11 a –
0.80 ± 0.05 aa
3.30 ± 0.16a –
3.12 ± 0.08– –
2.72 ± 0.11
1.03 ± 0.08
3.52 ± 0.20
2.76 ± 0.17
0.09 ± 0.02
0.04±0.007 b
0.1 ± 0.004 – c
0.08 ± 0.01
0.15 ± 0.05
0.08 ± 0.009 b 0.15 ± 0.01 – b
0.13 ± 0.01
0.24 ± 0.05
0.12 ± 0.02 b
0.20 ± 0.02
26.10 ± 6.23
12.85 ± 0.51 b 22.41 ± 1.14 – a
Durpiø substratas
(kontrolë)
0.2 ± 0.01 – b
20.4 ± 2.55
8.9 ± 0.85
15.4 ± 2.08 c
10.9 ± 0.58 – b 11.76 ± 1.08 ñ
3.03 ± 0.14
1.22 ± 0.05
4.25 ± 0.19
2.49 ± 0.03
2.21 ± 0.16
0.96 ± 0.05 –
3.17 ± 0.21 a
2.31 ± 0.07 -
2.14 ± 0.03c –
1.01 ± 0.02 – –
3.15 ± 0.05 a –
2.12 ± 0.01 – –
0.06 ± 0.003
0.05 ± 0.003 0.03 ± 0.003 – – 0.05 ± 0.003 c
0.12 ± 0.003
0.08 ± 0.007 – 0.07 ± 0.007a – 0.09 ± 0.007 b
0.18 ± 0.003
0.13 ± 0.01 –
20.09 ± 0.64
17.81 ± 0.16 – 15.7 ± 0.71 – – 17.87 ± 0.62 –
0.10 ± 0.01 – –
%
Stem length / Stiebo ilgis, ñm
Chl à, mg/dm2
Chl b, mg/dm2
Ñhl à+b, mg/dm2
Chl à/b, mg/dm2
Monosugars
Monocukrûs, %
Saccharose / Sacharozë, %
Sugar concentration
Cukraus koncentracija, %
Dry matter content / Sausøjø
medþiagø kiekis, %
Mean for
factor À
peat substrate
(control)
Mean for factor  / B faktoriaus vidurkis
6.4 ± 1.02
11.05 ± 1.92 c 8.2 ± 1.08 – a
3.03 ± 0.11
2.43 ± 0.13 c 2.32 ± 0.08 c –
1.19 ± 0.07
1.04 ± 0.07- 0.91 ± 0.05 b –
3.34 ± 0.21 b 3.22 ± 0.08 b –
4.22 ± 0.18
2.40 ± 0.22 – 2.62 ± 0.19 – –
2.57 ± 0.08
0.08 ± 0.01
0.04 ± 0.004 b
0.07 ± 0.01 – a
0.13 ± 0.02
0.08 ± 0.005 b
0.11 ± 0.22 – a
0.21 ± 0.03
0.12 ± 0.01 b
0.18 ± 0.03 – a
23.1 ± 3.11
15.33 ± 0.97 a 19.05 ± 1.41 – –
65
2.46 ± 0.14 a
1.06 ± 0.04 –
3.66 ± 0.18 –
2.31 ± 0.05 a
0.13 ± 0.01 b
T h e s e c o n d s t a g e o f a d a p t a t i o n. The results of the
represented researches allowed estimating the after-effect of substrates on biochemical
parameters of the adapted plants after transplantation during the second stage. Both
ion exchange substrates stimulated the growth of the stem and chlorophyll synthesis
for the both rootstocks (Table 3). The most prolonging positive effect on the Chl a
+ b synthesis was marked using the substrate BIONA-112. Depending on the genotype,
the influence of the ion exchange substrates was different: for the rootstock VSL-2
the kind of ion exchange substrate did not influence the accumulation of the
chlorophylls. For the rootstock OVP-2 on the substrate BIONA-312 was marked the
increase of the sum of chlorophylls, while BIONA-112 was increasing the
accumulation of Chl a.
T a b l e 3. Biochemical parameters characterizing physiological
development of rootstocks at the post-adaptation stage, n = 4
3 l e n t e l ë. Biocheminiai rodikliai, charakterizuojantys fiziologiná
poskiepiø vystymàsi po adaptacijos, n = 4
Forms of
rootstocks
(factor
A)
OVP-2
Poskiepiø
formos (A
faktorius)
Adaptation substrates (factor Â)
Adaptacijos terpës (B faktorius)
Biochemical
parameters
Mean for
factor À
Peat substrate
(control)
BIONA-112
BIONA-312
A faktoriaus
vidurkis
Δ stem length,
stem length
stiebo ilgis, ñm
0.3 ± 0.49
4.2 ± 0.27
2.5 ± 1.189.2 ± 0.82 b
–1.08 ± 0.98 – –
4.4 ± 0.71 – b
0.57±0.66
5.9 ± 0.77
Δ Chl a, mg/dm2
Chl a
0.21 ± 0.12
3.24 ± 0.19
1.78 ± 0.20 c
4.42 ± 0.10c
1.10 ± 0.15 cb
3.59 ± 0.20 – c
1.03 ± 0.21
3.75 ± 0.17
Δ Chl b, mg/dm2
Chl b
–0.09 ± 0.15
1.07 ± 0.04
0.32 ± 0.13 a
1.44 ± 0.04 b
0.51 ± 0.06 b –
1.32 ± 0.09 a-
0.25 ± 0.1
1.28 ± 0.06
Δ Chl à + b, mg/dm2
Chl a +b
0.12 ± 0.19
4.31 ± 0.18
2.35 ± 0.30 c
1.61 ± 0.21 ca
5.86 ± 0.13 c
4.91 ± 0.30 ab
1.36 ± 0.30
5.02 ± 0.22
Chl à/b, mg/dm2
Chl a/b
3.03 ± 0.22
3.07 ± 0.08 –
2.74±0.05 – –
2.95±0.08
Δ monosugars,
monosugars
monocukrûs, %
0.04 ± 0.006
0.13 ± 0.02
0.06 ± 0.01 a
0.1 ± 0.005 a
Δ saccharose
saccharose / sacharozë,
%
0.1 ± 0.04
0.25 ± 0.07
0.05 ± 0.009 –
0.13 ± 0.003 a
0.1 ± 0.02 – –
0.26 ± 0.01 – a
0.08 ± 0.02
0.21 ± 0.03
Δ sugar concentration,
sugar concentration
cukraus koncentracija, %
0.14 ± 0.04
0.37 ± 0.03
0.11 ± 0.020.23 ± 0.01 a
0.09 ± 0.03 – –
0.35 ± 0.02 – –
0.11 ± 0.02
0.31 ± 0.03
9.82 ± 6.54
35.92 ± 1.07
21.87 ± 1.80 a
34.72 ± 1.86-
9.59 ± 2.44 – a
13.8 ± 2.78
32.00 ± 1.86 – – 34.21 ± 0.99
Biocheminiai rodikliai
Δ dry matter content
dry matter content
sausøjø medþiagø kiekis, %
Durpiø substratas
(kontrolë)
66
– 0.009 ± 0.006 cc 0.03 ± 0.009
0.09 ± 0.004 b – 0.11 ± 0.008
T a b l e 3 continued
3 lentelës tæsinys
Forms of
rootstocks
Biochemical
(factor
parameters
A)
Biocheminiai parametrai
Adaptation substrates (factor Â)
Adaptacijos terpës (faktorius B)
Poskiepiø
formos (A
faktorius)
VSL-2
Δ stem length
stem length
stiebo ilgis, ñm
Mean for
factor À
A faktoriaus
vidurkis
– 0.13 ± 1.18
8.8 ± 0.78
10.2 ± 3.70 b
25.6 ± 2.37
3.7 ± 0.70 – a
14.7 ± 1.02 bc
4.6 ± 1.75 a
16.3 ± 2.25 ñ
Δ Chl a, mg/dm2
Chl a
0.04 ± 0.1
3.07 ± 0.12
1.02 ± 0.19 c
3.42 ± 0.07 –
0.87 ± 0.007 b –
3.01 ± 0.09 – –
0.70 ± 0.16 a
3.17 ± 0.07 c
Δ Chl b, mg/dm2
Chl b
– 0.28 ± 0.06
0.94 ± 0.08
0.18 ± 0.12 b
1.14 ± 0.09 –
0.05 ± 0.01 a – – 0.02 ± 0.07 b
1.06 ± 0.02 – – 1.04 ± 0.04 c
Δ Chl à + b, mg/dm2
Chl à + b
– 0.24 ± 0.16
4.01 ± 0.19
1.39 ± 0.31 c
4.55 ± 0.14 –
0.92 ± 0.09 b –
4.07 ± 0.11 – –
0.69 ± 0.23 b
4.21 ± 0.11 c
Chl à/b, mg/dm2
Chl à/b
3.32 ± 0.14
3.05 ± 0.19-
2.84 ± 0.04 a –
3.07 ± 0.09 –
Δ monosugars
monosugars
monocukrûs, %
0.05 ± 0.003
0.10 ± 0.003
0.06 ± 0.0050.10 ± 0.003
0.06 ± 0.003 – – 0.05 ± 0.003 c
0.09 ± 0 –
0.1 ± 0.002 –
Δ
saccharose,saccharose
sacharozë, %
0.07 ± 0.02
0.19 ± 0.02
0.12 ± 0.02 –
0.20±0.02 –
0.1 ± 0.004 – –
0.17 ± 0.01 – –
0.1 ± 0.01 –
0.19 ± 0.008 –
Δ sugar concentration
sugar concentration
cukraus koncentracija, %
0.12 ± 0.02
0.29 ± 0.02
0.18 ± 0.02 –
0.30 ± 0.02 –
0.16 ± 0.003 – –
0.26 ± 0.01 – –
0.15 ± 0.01 –
0.28 ± 0.01 –
Δ dry matter content
dry matter content
sausøjø medþiagø kiekis,
%
7.61 ± 1.35
27.70 ± 0.99
10.21 ± 0.96 –
28.02 ± 0.88 –
10.81 ± 1.52 – – 9.54 ± 0.80 a
26.5 ± 1.63 – – 27.41 ± 0.66 c
Mean for factor  / B faktoriaus vidurkis
Δstem length,
stem length / stiebo ilgis, ñm
0.08 ± 0.60
6.5 ± 0.94
6.3 ± 2.31 b
17.4 ± 3.31 c
1.3 ± 1.06 – a
9.5 ± 2.02 ac
ΔChl a, mg/dm2
Chl a
0.13 ± 0.08
3.15 ± 0.11
1.49 ± 0.17 c
3.92 ± 0.20 c
0.99 ± 0.09 cb
3.30 ± 0.15-c
ΔChl b, mg/dm2
Chl b
– 0.19 ± 0.08
1.0 ± 0.05
0.25 ± 0.09 c
1.29 ± 0.07 c
0.28 ± 0.09 c –
1.19 ± 0.07 a –
ΔChl à+b, mg/dm2
Chl à+b
– 0.06 ± 0.13
4.16 ± 0.14
1.87 ± 0.27 c
5.21 ± 0.26 c
1.27 ± 0.17 ca
4.49 ± 0.22-b
Chl à/b, mg/dm2
3.17 ± 0.13
3.06 ± 0.1 –
2.79 ± 0.03 a –
Δmonosugars,
monosugars / monocukrûs, %
0.04 ± 0.004
0.12 ± 0.01
0.06 ± 0.005 a
0.10 ± 0.003 –
0.02 ± 0.01 ac
0.09 ± 0.002 a –
67
T a b l e 3 continued
3 lentelës tæsinys
Forms of
rootstocks
Biochemical
(factor
parameters
A)
Biocheminiai parametrai
Mean for
factor À
Adaptation substrates (factor Â)
Adaptacijos terpës (faktorius B)
A faktoriaus
vidurkis
Poskiepiø
formos (A
faktorius)
Δ saccharose,
saccharose / sacharozë, %
0.09 ± 0.02
0.22 ± 0.03
0.08 ± 0.02 –
0.16 ± 0.02 –
0.10 ± 0.009 – –
0.21 ± 0.02 – –
Δsugar concentration,
sugar concentration /
cukraus koncentracija, %
0.13 ± 0.02
0.33 ± 0.04
0.14 ± 0.02 –
0.26 ± 0.02 –
0.13 ± 0.02 – –
0.30 ± 0.02 – –
8.71 ± 3.12
31.81 ± 1.69
16.04 ± 2.40 a
31.37 ± 1.58 –
10.20 ± 1.35 – –
29.96 ± 1.54 – –
Δdry matter content,
dry matter content
sausøjø medþiagø kiekis, %
For the both rootstocks steering of synthesis of monosugars was marked for
the plants, which were originally adapted on the BIONA-112, and saccharose and
soluble sugars were in general accumulated independently on the adaptation substrate.
During the second stage of adaptation the leveling of the quantity of dry matter
content by the adapted plants on all the substrates was marked. The minimum dry
matter content detected on the substrate BIONA-112, after the first adaptation stage
relevantly increased because of active accumulation of components, from which
dry matter is composed.
Conclusions. Trustworthy influence and post-influence of the adaptive
substrates on the biochemical data of the rootstocks of sour cherry was estimated.
On the first adaptation stage, a tendency to maximum accumulation of
photosynthetic pigments, sugars in the unit area and dry substance for the plants,
cultivated on the peat substrate is registered. Ion exchange substrate BIONA-312
provided the sugar synthesis and accumulation of dry matter more actively than
BIONA-112 (the substrate with higher concentration of mineral salts).
The rootstocks originally adapted on the substrate BIONA were characterized
by more intensive accumulation of chlorophylls (a, and sum of chlorophylls), the
quantity of it by the end of the second stage exceeding the data for adapted on the
peat substrate rootstock. Intensive accumulation of dry substances by the rootstocks,
which were transplanted from substrate BIONA-112 led to leveling this value in all
adapted regenerates.
Gauta
2006 05 12
Parengta spausdinti
2006 07 17
68
References
1. Á à õ í î â à Ê. Â., Ì è ë ü ê å â è ÷ Æ. À., Î ë ü ø à í è ê î â à À.
Ë., Â å ð á è ö ê à ÿ Í. À. Õàðàêòåðèñòèêà ïðîäóêöèè, âûðàùåííîé íà
öåîëèòñîäåðæàùåì ñóáñòðàòå ÁÈÎÍÀ-211 è ïî÷âîãðóíòå // Èçâåñòèÿ
Àêàä. àãðàð. íàóê ÐÁ. 1999. ¹. 2. C. 45–48.
2. à è ã î ë î ø â è ë è Ò. Ñ. Àíàòîìî-ôèçèîëîãè÷åñêèå îñîáåííîñòè
êóëüòóðàëüíîãî ìîðôîòèïà êàðòîôåëÿ (Solanum tuberosum L.) â óñëîâèÿõ
áèîòåõíîëîãè÷åñêîãî ïðîèçâîäñòâà.// Âåñöi Íàö. Àêàä. íàâóê Áåëàðóñi.
Ñåð. áiÿëàãi÷. íàâóê. 2000. ¹. 2. C. 27–30.
3. Ê à ð ì à í å í ê î Í. Ì., Ê à ç à í ö å â à Î. Ô. Êîëîðèìåòðè÷åñêèé
ìåòîä îïðåäåëåíèÿ ñàõàðîâ â ðàñòèòåëüíîì ìàòåðèàëå // Àãðîõèìèÿ.
1986. ¹. 1. C. 107–110. Ñ ìîäèôèêàöèÿìè.
4. Ê î ÷ ó á å é Ñ. Ì., Â î ë î â è ê Î. È., Ê î ð í å å â Ä. Þ.,
Ï î ð ó á ë å â à Ë. Â., Ø å â ÷ å í ê î Â. Â. Îðãàíèçàöèÿ è ôóíêöèîíàëüíàÿ
àêòèâíîñòü ôðàãìåíòîâ ìåæãðàíàëüíûõ è ãðàíàëüíûõ òèëàêîèëîâ ãîðîõà //
Ôèçèîëîãèÿ ðàñòåíèé. 1998. Ò. 45(6). C. 805–812.
5. Ì à ò ó ñ å â è ÷ Â. Â., Ñ å ì å í î â à Ç. À., Õ è ð ñ à í î â à È. Ô.
Ðàçìíîæåíèå êàðòîôåëÿ ÷åðåíêîâàíèåì íà èîíèòíûõ ïèòàòåëüíûõ ñóáñòðàòàõ
ðàçëè÷íîãî ñîñòàâà // Âåñöi ÍÀÍ Áåëàðóñi. Ñåðûÿ áiÿëàãi÷íûõ íàâóê.
1995. ¹. 2. C. 53–57.
6. Ì å ò î ä û áèîõèìè÷åñêîãî èññëåäîâàíèÿ ðàñòåíèé / ïîä ðåä. ä.á.í.
À.È. Åðìàêîâà Ë. – «Àãðîïðîìèçäàò» Ëåí. îòäåëåíèå, 1987. 432 ñ.
7. Ì è õ à é ë î â à Ñ. À., Ê ë è ì î â è ÷ À. Ñ., Ê à á à ø í è ê î â à
Ë. Ô. è äð. Âëèÿíèå ïðåäïîñåâíîé îáðàáîòêè ñåìÿí ÿ÷ìåíÿ ÿíòàðíîé
êèñëîòîé íà ðîñò ðàñòåíèé è èõ ðîäóêòèâíîñòü // Âåñöi ÍÀÍ Áåëàðóñi.
Ñåð. áiÿëàãi÷. íàâóê. 1997. ¹. 2. C. 53–56.
8. Ñ â i ð ø ÷ ý ó ñ ê à ÿ Ã. Ì., Ì à ò ó ñ å â i ÷ Â. Â., Á à ð ç ÿ ê Â. Ñ.,
Áîðìàòàó
Ó.
ß.
Àäàïòàöûÿ ãåíàòû÷íûõ ðýãåíåðàíòàó öóêðàâûõ
áóðàêîó íà iùíààáìåííûõ ñóáñòðàòàõ // Âåñöi ÍÀÍ Áåëàðóñi. Ñåðûÿ
áiÿëàãi÷íûõ íàâóê. 1995. ¹. 4. C. 36–39.
9. Ñ î ë ä à ò î â Â. Ñ., Ï å ð û ø ê è í à Í. Ã., Õ î ð î ø ê î Ð. Ï.
Èîíèòíûå ïî÷âû. Ìèíñê: Íàóêà è òåõíèêà. 1978. 172 c.
10. C y ä å é í à ÿ Ñ. Â., Ò è ì î ô å å â à Â. À. Âåãåòàòèâíîå ðàçìíîæåíèå
Peperomia caperata, Ficus benjamina íà èîíèòíûõ ñóáñòðàòàõ // Èçó÷åíèå
áèîðàçíîîáðàçèÿ ôëîðû Áåëàðóñè è îáîãîùåíèå ãåíîôîíäà êóëüòóðíûõ
ðàñòåíèé: Ìàò-ëû ìåæâóçîâñêîãî ñåìèíàðà áîòàíè÷åñêèõ êàôåäð ïî
ïðîáëåìàì áèîðàçíîîáðàçèÿ ôëîðû è ñåëåêöèè êóëüòóðíûõ ðàñòåíèé
24–26 àïðåëÿ 2002 ãîäà. 2003. C. 80–83.
11. Ñ ó ä å é í à ÿ Ñ. Â., Ó ò û ð î Ë. Á. Èñïûòàíèå èîíîîáìåííûõ
ñìîë â êà÷åñòâå ñóáñòðàòîâ ïðè âåãåòàòèâíîì ðàçìíîæåíèè ïåðñïåêòèâíûõ
ñîðòîâ Ribes nigrum L. // Îáîãàùåíèå è ñîõðàíåíèå ãåíîôîíäà íà îñíîâå
ïîâûøåíèÿ áèîëîãè÷åñêîãî ïîòåíöèàëà ðàñòèòåëüíûõ ðåñóðñîâ:
Ñá. íàó÷. òðóäîâ. – Ìí. ÁÃÏÓ èì. Ì. Òàíêà. 2000. C. 89–92.
12. Ò ó ë à å â à Ì. È., Ñ ò û ö ê î Ñ. À., Á å ë ÿ ê î â à Ç . Í . è
äð. Ìèêðîêëîíàëüíîå ðàçìíîæåíèå âèíîãðàäà íà èîíèòíûõ ñóáñòðàòàõ //
Ñàäîâîäñòâî è âèíîãðàäàðñòâî. 1990. ¹. 9. C. 14–16.
69
13. M c C l e l l a n d M. T., S m i t h M. A. L. C a r o t h e r s Z. B.
The effect of in vitro and ex vitro root initiation on subsequent microcutting root quality
in the woody plants.// Plant Cell Tiss. Organ Cult. 1990. No. 23. P. 115–123.
14. V e g v á r i G., V é r t e s y J. Further information to the acclimatization of
«in vitro» // International Journal of Horticultural Science. 1999. Vol. 5. No. 3–4. P. 54–58.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 62–70.
JONØ MAINØ TERPËS (BIONA-112 IR BIONA-312) ÁTAKA PRUNUS L.
POSKIEPIØ BIOCHEMINIAMS RODIKLIAMS ADAPTACIJOS EX VITRO
METU
T. Krasinskaya, N. Kukharchyk
Santrauka
Po in vitro kultûros adaptacijos ex vitro metu augaluose vyksta morfologiniai ir
fiziologiniai pokyèiai.
Adaptacijai pagerinti taikomi skirtingi metodai. Vienas jø – jonizuotø dirvoþemiø,
kaip adaptacijos substratø, panaudojimas. Mûsø tyrimo tikslas buvo iðtyrinëti augalo
fiziologiná vystymàsi ant Prunus L. poskiepiø, pavyzdþiui, VSL-2 (Prunus fruticosa (Pall.)
G. Waron. x P. lannesiana Carr.) ir OVP-2 (P. cerasus x P. Maackii), skirtingos mineralinës
sudëties (BIONA-112 ir BIONA-312) jonø mainø terpëje (JMT) adaptuojant ex vitro
aseptinëmis sàlygomis.
Augalo fiziologinis vystymasis buvo ávertintas pagal ðiuos biocheminius rodiklius:
chlorofilo (a + b) kieká (mg/dm2), cukraus koncentracijà (gliukozë + sacharozë) (%) ir sausøjø
medþiagø kieká (%).
Mûsø tyrimai parodë reikðmingà JMT átakà chlorofilo, cukraus ir sausøjø medþiagø
kaupimuisi. Antrajame adaptacijos etape buvo pastebëta esminë pozityvi jonø mainø
adaptacinës terpës átaka augalo fiziologiniam vystymuisi.
Reikðminiai þodþiai: Prunus L., jonø kaitos substratas, BIONA-112, BIONA-312,
biocheminiai rodikliai, chlorofilas, tirpûs cukrûs, sausøjø medþiagø koncentracija,
ex vitro, adaptacija, Baltarusija.
70
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 71–76.
LATERAL ROOT INDUCTION BY BACTERIA, RADICLE
CUT OFF AND IBA TREATMENTS OF ALMOND
CVS. ‘TEXAS’ AND ‘NONPAREIL’ SEEDLINGS
Emine ORHAN1, Sezai ERCISLI1, Ahmet ESITKEN1,
Fikrettin SAHIN2
1
Ataturk University, Agricultural Faculty, Department of Horticulture, 25240
Erzurum-Turkey. E-mail: [email protected]
Yeditepe University, Faculty of Engineering and Architecture, Department of
Genetics& Bioengineering, 34755 Kayisdagi-Istanbul, Turkey
2
This study was conducted to evaluate the effects of radicle cut off, IBA (50 and
100 ppm) and three Agrobacterium rubi (A1, A16 and A18) and a Bacillus subtilis strain
(OSU-142) alone or in combination with radicle cut off on seedling height, stem diameter,
number of lateral roots, root length, fresh and dry root weight. Seedlings of two almond
cvs. ‘Texas’ and ‘Nonpareil’ were studied. The results showed that seed treatment with
IBA, radicle cut off, bacteria alone or in combination with radicle cut off significantly
increased the number of lateral roots and fresh and dry root weight compared with the
control treatments. Highest number of lateral roots (8.89) was obtained from seeds treated
with Agrobacterium rubi A18 strain for cv. ‘Texas’ and A16 for cv. ‘Nonpareil’ (9.60).
Key words: almond, bacteria, lateral root formation, rootstock.
Introduction. Turkey is one of the significant and unique countries in the world
from the point of almond genetic resources and diversity. Ten Amygdalus species
have been reported in Turkey so far (Ercisli, 2004). In Turkey, up to 1980’s, almond
production was generally maintained by propagation by seeds (Unal et al., 1994).
However, recently some native and especially standard foreign varieties, such as
‘Texas’, ‘Nonpareil’ and ‘Ne Plus Ultra’, are being reproduced by budding in Turkey.
The budding method is spreading throughout the country and it is practiced either at
the nursery or in the seedbeds.
Notable lateral root difficulties exist in germinating seed of almond, using
conventional methods (Kuden et al., 1993). Due to the tap root formation, the ratio
of take in almond seedlings is very low this way establishing the orchards (Unal et
al., 1994). In nursery fruit tree production, a well developed and branching root
system is a prerequisite for a high ratio of take (Mulas et al., 1989). Therefore,
people have attempted to eliminate tap rooting of almond seedlings generally using
radicle cut off (Kuden et al., 1995; Akca and Ceylan, 1996). Since traditional radicle
cut off methods for lateral branching of almond roots is very time consuming and
needs extensive laboring, it is necessary to explore the easiest solutions.
71
Recent studies confirm that the application of bacteria in several genera
(Agrobacterium, Bacillus, Streptomyces, Pseudomonas and Alcaligenes) seed and
vegetative propagation materials induce new root formation in cuttings and seeds of
some plant species (Patena et al., 1988; Trip and Stomp, 1997; Ercan et al., 1999).
In previous studies, we used Agrobacterium rubi strains (A1, A16 and A18) in kiwifruit,
sour cherry and rose hip cuttings to induce rooting. These bacterial strains were
found to be more effective on the adventitious root formation compared to control
(Ercisli et al., 2003; Esitken et al., 2003; Ercisli et al., 2004).
The objective of the present study was to investigate the effect of radicle cut
off, IBA and bacterial treatments using Agrobacterium rubi (A1, A16, A18) and
Bacillus subtilis strain (OSU-142) alone or in combination with radicle cut off on the
lateral root formation of two almond cultivars ‘Texas’ and ‘Nonpareil’.
Materials and Methods. Seeds were taken from healthy almond trees ‘Texas’
and ‘Nonpareil’ at the harvest time in 2005 and then placed into moist perlitte media
in cold storage (4°C) for 30 days in order to break embryonic dormancy. After
stratification, seeds were subjected to one of the following twelve treatments:
1- Control
7- Agrobacterium rubi A18
2- Radicle cut off
8- Bacillus subtilis (OSU-142)
3- IBA (50 ppm)
9- Radicle cut off + Agrobacterium rubi A1
4- IBA (100 ppm)
10-Radicle cut off + Agrobacterium rubi A16
5- Agrobacterium rubi A1
11-Radicle cut off + Agrobacterium rubi A18
6- Agrobacterium rubi A16 12- Radicle cut off + Bacillus spp. (OSU-142)
For radicle cut off treatments, the basal portion of radicles were cut by pinching
about 0.5-1.0 mm. Bacterial treatments were performed by dipping the seeds into the
suspension of Agrobacterium rubi (strains A1, A16 or A18) and Bacillus subtilis (strain
OSU-142) prepared in sterile water at a concentration of 109 cfu/ml. IBA treatments
were also performed by dipping the seeds into IBA solution for 10 min at a concentration
of 50 and 100 ppm. Radicle cut off + bacteria combined treatments were achieved by
dipping radicle cut off seeds into the bacterial suspension. Seeds in the control group
were dipped in sterile water. Following treatments, treated seeds were planted in plastic
bags filled with turf media in a greenhouse maintained at 21±2°C.
Plant height, stem diameter, number of lateral roots, root length, and fresh and
dry root weight were determined on 30 randomly chosen seedlings for each treatment.
The experimental design was a randomized complete block with 3 replications. Each
replication contained 20 seeds. Data were subjected to analysis of variance (ANOVA).
Means were separated using Duncan’s multiple range tests.
Results. The effect of all treatments tested in this study on the plant height,
stem diameter, number of lateral roots, root length and fresh and dry root weight of
almond cvs. ‘Nonpareil’ and ‘Texas’ are summarized in Table. The data demonstrated
that, there were statistical differences in ‘Nonpareil’ but not cv. ‘Texas’ seedling
height among the treatments (Table). The highest plant height (64.80 cm) was obtained
when cultivar ‘Nonpareil’ was treated with Agrobacterium rubi A16 and followed by
radicle cut off + A16 treatment (63.33 cm) (Table).
72
T a b l e. Effects of IBA, bacteria, radicle cut off, bacteria plus radicle
cut off on almond seedling growth parameters
L e n t e l ë. ISR, bakterijø, ðakneliø trumpinimo ir bakterijø bei ðakneliø
trumpinimo derinio átaka migdolø sëjinukø augimo rodikliams
Treatments
Variantai
Height
Aukštis,
cm
Stem
diameter
Number of
lateral roots
Root
length
Fresh root
weight
Dry root
weight
Kamieno
Ðalutiniø ðaknø Ðaknø ilgis, Þalioji ðaknø Sausoji ðaknø
skaièius
skersmuo, mm
masë, g
masë, g
cm
‘Texas’
57.86
3.86
2.43 by
25.14
5.30 c
3.38 c
63.40
3.60
7.17 a
29.30
7.98 abc
4.52 abc
IBA (50 ppm)
58.18
3.84
7.63 a
26.24
7.17 abc
4.10 abc
IBA(100ppm)
59.33
3.92
7.92 a
27.56
7.43 abc
4.23 abc
Control /
Kontrolinis variantas
R. cut off / Ðakneliø
patrumpinimas
A1
58.14
4.00
8.40 a
24.57
7.37 abc
4.70 abc
A 16
56.75
4.03
8.50 a
27.50
7.92 abc
5.36 ab
5.03 abc
A 18
59.43
3.93
8.89 a
27.14
7.71 abc
OSU 142
63.67
4.03
8.00 a
27.00
6.27 bc
3.55 bc
RC+A 1
58.33
3.60
8.75 a
27.00
8.86 ab
4.67 abc
RC+A 16
59.33
3.85
8.75 a
27.50
7.82 abc
4.18 abc
RC+A 18
62.71
3.69
8.44 a
27.86
9.69 a
4.98 abc
RC+OSU142
62.25
3.86
8.88 a
30.13
9.89 a
5.56 a
NS
NS
1.68
NS
2.58
1.56
43.00 b
3.31 d
1.63 d
23.88
5.00 c
2.60 c
44.50 cd
3.80 bc
6.11 c
23.88
6.69 bc
3.93 b
LSD01 / R01
‘Nonpareil’
Control /
Kontrolinis variantas
R. Cut Off / Ðakneliø
patrumpinimas
IBA (50 ppm)
45.62 cd
3.42 d
4.82 de
23.40
5.24 bc
2.32 c
IBA(100ppm)
46.30 cd
3.55 cd
5.13 d
23.22
5.38 bc
2.47 c
A1
46.00 cd
3.28 d
5.60 d
23.75
5.85 bc
2.40 c
A 16
64.80 a
4.26 a
9.60 a
28.00
10.79 a
6.24 a
A 18
45.50 d
3.54 cd
6.20 c
22.60
5.43 bc
2.65 c
OSU 142
51.75 bcd
3.95 ab
5.00 d
23.00
6.10 bc
3.15 bc
RC+A 1
52.90 bcd
3.72 bc
7.60 b
23.70
6.09 bc
4.44 b
RC+A 16
63.33 ab
3.57 cd
8.86 a
25.89
5.46 bc
3.60 bc
RC+A 18
52.63 bcd
3.98 ab
7.69 b
26.50
6.69 bc
4.08 b
RC+OSU142
54.80 bc
3.73 bc
9.43 a
24.14
7.13 b
4.39 b
9.47
0.36
0.93
NS
1.89
1.24
LSD01 / R01
* Means in columns followed by a different letter differ significantly, NS: Non Significant
Skirtingomis raidëmis paþymëtø reikðmiø stulpeliuose skirtumai yra esminiai; NS: skirtumai
neesminiai
73
Bacteria treatments of cultivar ‘Nonpareil’ caused statistically different plant
heights (p≤0.01, Table). The highest plants were observed with inoculated bacteria
strain, Agrobacterium rubi (A16) – 64.80 cm and followed by Bacillus subtilis
(OSU-142) – 51.75 cm, respectively (Table). The differences of the stem diameter
of cultivar ‘Nonpareil’ based on treatments given in Table 1 showed that maximum
stem diameter was obtained from Agrobacterium rubi A16 (4.26 mm) and followed
by radicle cut off + A18 treatment (3.98 mm) (Table).
The data showed that bacterial treatment alone or in combination with radicle
cut off significantly increased the number of lateral root and fresh and dry root
weight in both tested almond cultivars (Table). The number of lateral roots was
highest in Agrobacterium rubi A18 treatment (8.89) of ‘Texas’ and A16 treatment
(9.60) of ‘Nonpareil’ (Table).
Different treatments exhibited varying degrees of fresh and dry root weight. All
treatments, except control, increased fresh and dry root weight in both ‘Texas’ and
‘Nonpareil’. Radicle cut off+OSU-142 treatment of ‘Texas’ and Agrobacterium rubi
A16 of ‘Nonpareil’ were found to be the most effective in terms of both fresh and
dry root weight (Table).
Discussion. This experiment was designed to investigate the effect of IBA,
bacteria, radicle cut off and bacteria + radicle cut off on lateral root formation of
almond seedlings of cvs. ‘Texas’ and ‘Nonpareil’.
The results obtained in the present study revealed that all seed treatments in two
almond cultivars resulted in significantly more lateral roots than water-treated seeds
(Table 1). The treatments with Agrobacterium rubi A18 of ‘Texas’ and Agrobacterium
rubi A16 of ‘Nonpareil’ was found to be most effective in terms of lateral root
induction. These results may suggest that the differences in bacterial strain may be
an important factor for lateral root induction. It is evident that the seeds of different
plant species require different bacteria strains to promote lateral root formation.
These results support the findings of Ercan et al. (1999), who demonstrated that the
highest root numbers of Madder (Rubia tinctorum) populations were produced after
inoculation with Agrobacterium rhizogenes strains 15834, 2628, R1000 and 9365. It
has been shown previously that especially rooting might be induced in woody plants
by inoculation with Agrobacterium strains. McAfee et al. (1993) showed that hairy
rooting of Pinus was higher when they were inoculated with Agrobacterium strains.
Ercisli et al. (2004) tested three bacteria strains for rooting rose hip cuttings and
found that Agrobacterium rubi A16 for genotype ERS 14 and A18 for genotype ERS
15 was the most effective. Caesar and Burn (1987) also observed that seedlings of
apple gave better lateral roots when treated with bacteria strains.
Conclusion. Bacteria alone or bacteria plus radicle cut off treatments appeared
to induce lateral root formation on treated seeds of Texas and Nonpareil almond
cultivars. These results indicated that bacteria alone or bacteria plus radicle cut off
may indeed be useful for lateral root formation on difficult to-lateral roots woody
species. It has been suggested previously that the stimulation of rooting by bacteria
is due to the production of IAA by the bacteria. Thus, it is possible to speculate that
the bacterial strains used in this study may be producing IAA. Further studies are
74
underway to investigate the exact function of these bacterial strains in promoting the
root production of almond seeds.
Gauta
2006 04 24
Parengta spausdinti
2006 08 04
References
1. Akça, Y., Ceylan S. A study on the comparison of some rootstock properties of
sweet and bitter almond seeds // Proceedings of Hazelnut and the Other Nut Fruits
Symposium, 10–11 January 1996, Samsun-Turkey. P. 402–408.
2. Caesar, A.J., Burr, T.J. Growth promoting of apple seedlings and rootstocks by
specific strains of bacteria // Phytopathology. 1987. 77(11): 1583–1588.
3. Ercan, A.G., Taskin, K.M., Turgut, K., Yuce, S. Agrobacterium rhizogenes-mediated
hairy root formation in some Rubia tinctorum L. populations grown in Turkey // Turkish
Journal of Botany. 1999. 23:373–378.
4. Ercisli, S. A short review on the fruit germplasm resources of Turkey // Genetic
Resources and Crop Evaluation. 2003. 51:419–435.
5. Ercisli, S., Esitken, A., Cangi, R., Sahin, F. Adventitious root formation of kiwi fruit
in relation to sampling data, IBA and Agrobacterium rubi inoculation // Plant Growth
Regulation. 2003. 41(2):133–137.
6. Ercisli, S., Esitken, A., Sahin, F. Application of exogenous IBA and inoculation with
Agrobacterium rubi stimulate adventitious root formation among stem cuttings of two
rose genotypes // HortScience. 2004. 39(3):533–534.
7. Esitken, A., Ercisli, S., Sevik, I., Sahin, F. Effect of Indole-3-Butyric Acid and Different
Strains of Agrobacterium rubi on Adventive Root Formation from Softwood and SemiHardwood Wild Sour Cherry Cuttings // Turkish Journal Agriculture and Forestry. 2003.
27, 37–42.
8. Kuden, A.B., Kaska, N., Kuden, A. Inducing the lateral root development of almond
seedlings: Comparing the foreign cultivars with some of our local cultivars for developing
lateral roots // Journal Agricultural Faculty of Cukurova University. 1993. 8(2):153–158.
9. Kuden, A.B., Kuden, A., Kaska, N. Comparing the foreign cultivars with some of
our local cultivars for developing lateral roots // Journal Agricultural Faculty of Cukurova
University. 1995. 10(4):149–158.
10. McAfee, B.J., White, E.E., Pelcher, L.E., Lapp, M.S. Root induction in Pine (Pinus)
and Larch (Larix) spp. using Agrobacterium rhizogenes // Plant Cell, Tissue and Organ
Culture. 1993. 34, 53–62.
11. Mulas, M., Delrio, G., D’Hallewin, G., Grassely, C. Etude de populations d’amendier
pour la selection de porte-greffes // Options Mediterraneennes Seria Seminaires. 1989.
5:39–46.
12. Patena, L., Sutter, E. G., Dandekar, A. M. Root induction by Agrobacterium
rhizogenes in a difficult-to-root woody species // Acta Horticulturae. 1988. 227:324–329.
13. Tripp, K.E., Stomp, A. M. Horticultural applications of Agrobacterium rhizogenes
(hairy-root): enhanced rooting of difficult-to-root woody plants // Combined Proceedings
of the International Plant Propagators’ Society. 1997. 47:527–535.
14. Unal, A., Gulcan, R., Misirli, A. A study on seedling rootstock properties of some
almond cultigens // Acta Horticulturae. 1994. 373:105–110.
75
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 71–76.
‘TEXAS’ IR ‘NONPAREIL’ VEISLIØ MIGDOLØ SËJINUKØ ÐALUTINIØ
ÐAKNØ AUGIMO SKATINIMAS BAKTERIJOMIS, ÐAKNELIØ TRUMPINIMU
IR ISR
E. Orhan, S. Ercisli, A. Esitken, F. Sahin
Santrauka
Ðio tyrimo tikslas – ávertinti ðakneliø trumpinimo, IBA (50 ir 100 ppm) ir trijø
Agrobacterium rubi (A1, A16 ir A18) bei Bacillus subtilis ðtamø (OSU-142) – vienø arba
derinant su ðakneliø ðalinimu bei bakterijomis – átakà dviejø migdolø veisliø (‘Texas’ ir
‘Nonpareil’) sëjinukø aukðèiui, kamieno skersmeniui, ðalutiniø ðaknø skaièiui, ilgiui, þaliajai
ir sausajai masei. Rezultatai parodë, kad migdolø sëklø apdorojimas trumpinant ðakneles,
bakterijomis ir ISR arba derinant ðakneliø trumpinimà su bakterijø panaudojimu reikðmingai
padidino ðalutiniø ðaknø skaièiø bei þaliàjà ir sausàjà masæ, palyginti su kontroliniais
variantais. Daugiausia ðalutiniø ðaknø gauta ‘Texas’ sëklas apdorojus Agrobacterium
rubi A18 ðtamu (8.89), o ‘Nonpareil’ – A16 ðtamu (9.60).
Reikðminiai þodþiai: migdolai, bakterijos, ðalutiniø ðaknø formavimasis, poskiepiai.
76
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 77–84.
VEGETATIVE CHERRY ROOTSTOCKS IN TISSUE
CULTURE
Ewa DZIEDZIC, Monika MAÙODOBRY
Agricultural University, Pomology and Apiculture Department,
al. 29 Listopada 54, 31–425 Kraków, Poland. E-mail: [email protected]
Multiplication of three cherry rootstocks PHL-6, PHL-84 and F12/1 was carried out
on solid and two-phase medium according to MS medium. The effect of cytokinin BA,
auxins IBA and NAA on shoot multiplication was studied. Better shoot multiplication was
achieved on the media containing auxin IBA in comparison to multiplication on media with
NAA. Greater increase of fresh mass was noted on two-phase media. The rooting of
shoots was conducted on WPM medium with addition of IBA and IAA auxins. The
studied rootstocks did not differ in shoot length, number of roots and total length of roots
for one shoot. Micrografting of cv. ‘Regina’ on rootstocks Damil and Gisela 5 and cv. ‘Van’
on rootstock Damil was carried out using different grafting methods in vitro. High percent
of successful micrografts was achieved for ‘Regina’ and ‘Van’ on rootstock Damil.
Key words: cherry rootstocks, micrografting, rooting, two-phase medium.
Introduction. Vegetative cherry rootstocks are subject of great interest because
of their possibility to reduce cherry tree growth. However, before introduction into
big scale production they have to be comprehensively studied. Many of them are
able to propagate by tissue culture only. The micropropagation of dwarfing rootstocks
PHL-6 and PHL-84 (Erbenova et al., 2001; Sedlak et al., 2005) and vegetative clone
of Prunus avium F12/1 (Krasinskaya, Kukharchik, 2004) was already the subject of
propagation in tissue culture. The influence of double-phase medium on shoot
propagation and rooting was tested for pear (Viseur, 1987; Wang, 1991) and apple
rootstocks (Litwiñczuk, 2000). This micrografing procedure has been applied for
different purpose: production of disease-free plants (Déogratias et al., 1991; Barba
et al., 1995; Starrantino, Caruso, 1998), diagnosis of virus infection (Tanne et al.,
1993; Pathirana, McKenzie, 2005), study of graft compatibility and formation of the
graft union (Cantos et al., 1995), rejuvenation of shoots from adult plants (Mneney,
Mantel, 2001; Fernández-Lorenzo, Fernández-Lopez, 2005). Micrografting was applied
for many plants: grapevine, peach, apple, cashew, avocado, apricot, citrus, almond.
There are also protocols of micrografting for Prunus type (Gebhardt, Goldbach,
1988; Özzambak, Schmidt, 1991; Schmidt et al., 1997). The aim of present studies
was to investigate the usefulness of method in vitro for cherry rootstocks propagation
and micrografting using cherry cultivars and rootstocks.
77
Material and methods. The multiplication of cherry rootstocks PHL-6,
PHL-84, F12/1 was conducted on MS medium (Murashige, Skoog, 1962) using two
forms: solid (S) and double-phase (2 P) medium. The double-phase medium was
obtained by pouring 5 ml of liquid medium onto the medium solidified with agar
(25 ml) at the beginning of the subculture. Both types of media were completed with
BA (0.7 mg/l) and auxins, either IBA (0.1 mg/l) SM1 and 2PM1 or NAA (0.2 mg/l)
SM2 and 2PM2. The experiment was conducted in 5 replications; one consisted of
jar with 5 shoots. The experiment was repeated twice. The fresh mass increase and
the number of shoots obtained were recorded. The rooting stage was conducted on
WPM medium (Lloyd, McCown, 1980) with addition of IAA (5.0 mg/l) and IBA
(2.0 mg/l). The shoots used for rooting experiment were produced on solid medium
(SM1). There were 5 replications, each of one jar with 5 shoots. The percent of
rooted shoots, the number and total length of roots, percent of roots distribution
according to their length were recorded. For micrografting experiment the leaves
and the apical meristem were removed from shoots Gisela 5 and Damil
(1.5-2.0 cm in length) used as rootstock. Shoot-tip explants of ‘Regina’ and ‘Van’
used as scions were 0.2–0.3 and 0.4–0.5 cm in length, respectively (Table 1). Before
T a b l e. 1. Scion / rootstock combinations and types of treatments
applied for cherry micrografting
1
Exp.
Bandymas
1
l e n t e l ë. Skiepûglio ir poskiepio deriniai ir apdorojimo tipai, taikyti atliekant
vyðniø mikroskiepijimus
Scion
Skiepûglis
‘Regina’
Even end of
shoot-tip
explants
Lygus ûglio
virðûnës
eksplanto galas
2
‘Regina’
Even end of
shoot-tip
explants
Lygus ûglio
virðûnës
eksplanto galas
Rootstock
Pre-treatment
Poskiepis
Išankstinis apdorojimas
Gisela 5
Un-rooted
shoots
Neásiðaknijæ
ûgliai
Damil
Rooted
shoots
Ásiðaknijæ
ûgliai
Antioxidant solution A
Antioksidanto A tirpalas
Antioxidant solution B
Antioksidanto B tirpalas
Antioxidant solution A
Antioksidanto A tirpalas
Antioxidant solution B
Antioksidanto B tirpalas
Method of
grafting
Áskiepijimo
bûdas
Shoot-tip
grafting
Treatment
after
grafting
Apdorojimas
áskiepijus
Light
Sviesoje
Ûglio
virðûnës
áskiepijimas
Darkness 1
day
Shoot-tip
grafting
Darkness 6
days
Ûglio
virðûnës
áskiepijimas
1 para
tamsoje
6 paros
tamsoje
0.6% agar with 5 mg/l IAA on
the graft union
0,6% agaro su 5 mg/l IAA ant skiepo
3
‘Van’
Wedge shape
end of shoottip explants
Pleišto formos
ûglio virðûnës
eksplanto galas
Damil
Rooted
shoots
Ásiðaknijæ
ûgliai
Antioxidant solution A
Antioksidanto A tirpalas
Cleft
grafting
Áskëlimas
Antioxidant solution B
Antioksidanto B tirpalas
0.6% agar with 5 mg/l IAA on
the graft union
0,6% agaro su 5mg/l IAA ant skiepo
78
Darkness 6
days
6 paros
tamsoje
grafting the upper part of the rootstocks and the lower end of scions were dipped
for 1 min in antioxidant solution; solution A 150 mg/l citric acid, 0.1 mg/l GA3,
0.5 mg/l BA or solution B 150 mg/l citric acid, 0.1 mg/l GA3, 0.5 mg/l IBA. Moreover
in exp. 1 and 2 few drops of 0.6% agar with 5mg/l IAA was dropped around the
graft union. In exp. 3 the wedge shape end of scion ‘Van’ was inserted into
0.5–0.6 cm slit in rootstock Damil. The grafts were placed individually into testtubes on WPM medium. All media were enriched with sucrose (30 g/l), and agar
(7 g/l). The pH was adjusted to 5,7 before autoclaving. Explants were cultured at
24°/23°C, 16 h day/8 h night at fluorescence light 92.8 µmol m-2 s-1.
The results obtained at multiplication and rooting stage were statistically analyzed
using variance analysis method. To assess the significance of difference between
means, the Duncan’s test was used at the 5% level of significance.
Results. During the multiplication stage the relationships between investigated
parameters were proved. Type of applied media affected significantly the increase of
fresh mass and number of shoots (Table 2).
T a b l e 2. Effect of media type on increase of fresh mass and number
of shoots per one jar
2
l e n t e l ë.
Medium
Terpë
SM1
SM2
2PM1
2PM2
Terpës tipo átaka þaliosios masës ir ûgliø skaièiaus viename
indelyje padidëjimui
Increase of fresh mass
Þaliosios masës padidëjimas,
2.13 a*
2.18 a
3.70 c
3.14 b
Number of shoots
g
Ûgliø skaièius
21.8 bc
19.9 b
23.5 c
16.9 a
* Means followed by the same letters do not differ statistically at probability α = 0.05
Ta paèia raide paþymëtos reikðmës ið esmës nesiskiria (α = 0,05).
Distinctly the greatest increase of mass was obtained on double-phase media
(3.70 g on 2PM1 and 3.14 g on 2PM2 medium), however such a simple relationship
was not evidence for number of shoots. The least number of shoots was obtained on
2PM2 medium whilst the numbers of shoots on the other media were similar. Also
the successive subculture affected the investigated factors (Table 3).
Increase both of fresh mass (3.33 g) and number of shoots (24.2) was greater
in the first than in the second subculture. Comparing the subcultures in terms of
produced mass and obtained shoots one could state that only in the first subculture
the double-phase media resulted in very high increase of mass. Moreover the maximum
mean number of shoots (33.9) was recorded on double-phase medium containing
IBA (2PM1) in the first subculture. Analysis of variance showed significant relationship
between the type of medium, successive subculture and rootstocks in terms of
production of fresh mass and number of shoots. Double-phase media enabled obtaining
both greater fresh mass and number of shoots. Such interaction was proved for all
rootstocks. Renewed application of the same media gave opposite results. Application
79
of double-phase media in spite of undoubted advantages resulted in high percent
(nearly 100%) of vitrified shoots. Moreover, browning of shoot tips was noted. The
rootstocks produced differentiated numbers of short and long shoots depending on
the type of medium and subculture. For PH-L 6 and F12/1 rootstocks the doublephase media in the first subculture resulted in higher number of long shoots compared
to the corresponding solid media. Renewed application of double-phase media resulted
in decreasing of long shoot number (data not presented). The shoots rooted in 100%.
T a b l e 3. Increase of fresh mass and number of shoots depending
on type of media and successive subculture per one jar
3
l e n t e l ë. Þaliosios masës ir ûgliø skaièiaus padidëjimo priklausomumas nuo
terpës tipo ir tolesnës subkultûros viename indelyje
Subculture
Subkultûra
I
Medium
Terpë
Increase of fresh mass
Þaliosios masës padidëjimas,
Number of shoots
g
Ûgliø skaièius
SM1
1.28 a*
16.7 bc
SM2
1.70 b
17.4 c
2PM1
5.03 e
33.9 f
2PM2
5.32 e
28.8 e
2.99 d
2.66 cd
2.36 c
0.96 a
3.33 b
Mean for subculture I / I subkultûros vidurkis
Mean for subculture II /II subkultûros vidurkis
2.24 a
* Means followed by the same letters do not differ statistically at probability
Ta paèia raide paþymëtos reikðmës ið esmës nesiskiria (α = 0,05).
II
SM1
SM2
2PM1
2PM2
26.9 e
22.4 d
13.1 b
5.0 a
24.2 b
16.8 a
α = 0.05
The differences in shoot length, roots number per one shoot and total length of
roots among investigated rootstocks statistically were not essential (Table 4). The
shoots obtained were rather short and their mean length was from 1.2 cm (for
F12/1) to 1,4 cm (for PH-L 84). The recorded mean number of roots per one shoot
ranged from 10.0 (for F12/1) to 12.4 (for PH-L 84). The highest total length of roots
was noted for rootstock PH-L 6. The shoots produced the roots of different length.
For rootstock PH-L 6 roots of 2.5 cm in length predominated (23.3%), for PH-L 84
– 2.5 cm roots (22.1%), and for F12/1 – 3.0 cm roots (17.1%). The longest roots
(6.0 and 6.5 cm) were recorded for PH-L 6 rootstock.
In the micrografting experiment different pre-treatments of scions and stocks,
ways of grafting and light conditions after grafting affected the successful grafts
(Table 5).
Owing to pre-treatment plant tissue with antioxidant solutions A and B no
browning of scions and stocks cut surface was noted. The scions and stocks
treatments with solution B (containing auxin IBA) resulted in higher percent of
successful grafts in comparison to treatment with solution A. In exp.1 the darkness
of treatment after grafting affected the higher percent of successful grafts. In
80
exp. 3 the beneficial effect of cleft-grafting for cv. ‘Van’ and rootstock Damil comparing
to shoot-tips grafting (exp. 1 and exp. 2.) was proved by high percent of successful
grafts. The scions and stocks attached to each other closely and the percent of
graft-units displacements was low.
T a b l e 4. Mean number and mean overall length of roots, mean
length of shoots of cherry rootstocks (per one shoot)
4
l e n t e l ë.
Vyðniø poskiepiø ðaknø skaièiaus, bendro ilgio ir ûgliø ilgio
vidurkiai, tenkantys vienam ûgliui
Rootstock Mean number of roots
Poskiepis
Vidutinis ðaknø skaièius
PHL 6
PHL 84
F12/1
Mean overall length of roots
cm
Mean length of shoots
Vidutinis ûgliø ilgis, cm
28.8
27.8
25.8
1.2
1.4
1.2
Vidutinis bendras ðaknø ilgis,
10.6
12.4
10.0
T a b l e 5. Overall number of micrograft development efficiency with
different combination of scions and rootstocks of cherry
5
Exp.
Bandymas
1
l e n t e l ë.
Mikroûglio vystymasis taikant skirtingus vyðniø skiepûgliø ir
poskiepiø derinius
Pre-treatment
% of
% of
Scion / stock of scion and Treatment after
successful displacement % of dry
combination
stock
grafting
grafts
graft-units graft-units
Skiepûglio ir
poskiepio
derinys
‘Regina’
Gisela 5
Skiepûglio ir
poskiepio
išankstinis
apdorojimas
Apdorojimas
áskiepijus
Solution A
Light
A tirpalas
Šviesa
Darkness
Sëkmingi
áskiepijimai,
%
Skiepø
pasislinkimas,
%
Nudþiûvæ
skiepai, %
0
42.8
57.2
40.0
20.0
40.0
25.0
25.0
50.0
50.0
25.0
25.0
43.0
28.5
28.5
66.7
33.3
0
60.0
20.0
20.0
50.0
0
50.0
Tamsa 1 d.
2
‘Regina’
Damil
Solution B
Light
B tirpalas
Šviesa
Solution A
A tirpalas
Solution B
B tirpalas
3
‘Van’
Damil
Solution A
A tirpalas
Solution B
B tirpalas
Darkness
Tamsa 1 d.
Darkness
Tamsa 6 d.
Darknes
Tamsa 6 d.
Darkness
Tamsa 6 d.
Darkness
Tamsa 6 d.
Discussion. During propagation stage on solid medium with addition of
BA (0.7 mg/l) the highest coefficient of shoot propagation of F12/1 was 5.8. Similarly
Krasinskaya and Kukharchik (2004) at propagating of various Cerasus forms (among
them F12/1) achieved the best coefficient of shoot multiplication (5.5) on the solid
medium with addition of 0.75 mg/l BA and 3.0 mg/l GA3. Higher concentration of BA
caused better multiplication (coefficient 8.4) but the shoots vitrified in high degree.
For PH-L 6 and PH-L 84 rootstocks the acceptable coefficients were 5.2 and 5.5.
81
Erbenova et al. (2001) proved by 50% higher multiplication rate of the same rootstocks
at 1.5 mg/l BA, than 0.75 mg/l BA. Sedlak et al. (2005) for PH-L 84 rootstock
achieved the extremely high multiplication (10.9 shoots longer than 10 mm) on MS
medium with addition of 1.5 mg/l BA. According to Borkowska (1997), morphological
reaction to double-phase culture system is increasing fresh mass by increasing number
of shoots or length or enhancing the area of leaves. In presented studies distinctly
the greatest increase of mass was obtained on double-phase media, however such a
simple relationship was not evidence for number of shoots. Between the doublephase media only that one containing auxin IBA resulted in higher number of shoots.
Viseur (1987) proved that double-phase medium gave high yield of axillary shoots of
pear cv. Durondeau; 6–7 shoots comparing to 2–3 shoots for medium solidified with
0.5% agar. Wang (1991) found significant increasing of pear shoot number and
length on double-phase medium. It was interesting that adding liquid medium to onemonth-old cultures produced the similar effect on shoot multiplication as transferring
shoots onto a fresh solid medium. Studies carried out by Litwiñczuk (2000) showed
that the application of two-phase medium improved the shoot proliferation and
elongation in the case of apple rootstocks MM.106 and P 14 but not M.26. The
increase of fresh mass was achieved mainly due to abundant foliage. Rooting on
WPM medium with addition of IAA and IBA resulted in 100% of rooted shoots.
Often rooting of shoots is carried out on modified MS medium (Sedlak et al, 2005).
In the earlier study Dziedzic (2004) obtained better results at micrografts placed on
solid than on liquid medium because of graft-units vitrification and contamination of
liquid medium. Therefore in the presented study only the solid media were applied.
Similarly Özzambak and Schmidt (1991) found the solid media better than liquid
one. Success at micrografting depends on good adhesion of grafting units. At that
case the cleft-grafting seems to be more appropriate than simply sticking of two
parts of shoots. Moreover, the silicone tube can be applied to fasten grafts units
(Gebhardt, Goldbach, 1988; Özzambak, Schmidt, 1991; Dziedzic, 2004). At presented
experiment the maximum percent of successful grafts was 66.7%. Much better
results were obtained by Dobránszki (2000) 95% of successful grafts and Tanne et
al. (1993) 70–90% of successful grafts for grape sloping-grafting. Nas and Read
(2003) carried out very interesting and economically reasonable experiment proving
that it is possible simultaneous micrografting, rooting and acclimatizing with
successfully survival of grafts for grapevine (50%), hazelnut (70%) and American
chestnut
Conclusions. 1. Once appliance of double-phase medium increase both fresh
mass and number of shoots.
2. Rooting of cherry rootstock shoots should be preceded by elongation on the
media without cytokinin.
3. Cleft grafting method completed by pre-treatment of antioxidant solutions
can be recommended for cherry micrografting.
Gauta
2006 04 19
Parengta spausdinti
2006 07 17
82
References
1. B a r b a M., C u p i d i A., L o r e t i S., F a g g i o l i F. M. In vitro
micrografting: a technique to eliminate peach latent mosaic viriod from peach // Acta
horticulturae. 1995. Vol. 386. P. 531–535.
2. B o r k o w s k a B. Zastosowanie po¿ywek dwufazowych w pêdowych
kulturach in vitro // Materiaùy z Konferencji „Rozmnaýanie roúlin in vitro” Skierniewice,
1997. P. 5–11.
3. C a n t o s M., A l é s G., T r o n c o s o A. Morphological and anatomical
aspects of a cleft micrografting of grape explants in vitro // Acta horticulturae. 1995. Vol.
388. P. 135–140.
4. D é o g r a t i a s J. M., C a s t e l l a n i V., D o s b a F., J u a r e z J.,
A r r e g u i J. M., O r t e g a C., O r t e g a V., L l á c e r G., N a v a r r o
R. Study of growth parameters on apricot shoot-tip grafting in vitro (STG) // Acta
horticulturae. 1991. Vol. 293. P. 363–372.
5. D o b r á n s z k i J., M a g y a r - T á b o r i K., J á m b o r - B e n c z ú r
E., L a z á n y i J. New in vitro micrografting method for apple by sticking //
International Journal of Horticultural Science. 2000. 6(4). P. 79–83.
6. D z i e d z i c E. Wstæpne badania dotyczàce szczepienia czereúni (Prunus avium
L.) w warunkach in vitro // Folia Univ. Agric. Stetin, Agricultura. 2004. 240(96). P. 41–44.
7. E r b e n o v a M., P a p r s t e i n F., S e d l a k J. In vitro propagation of
dwarfed rootstocks for sweet cherry // Acta horticulturae. 2001. Vol. 560. P. 477–480.
8. F e r n á n d e z - L o r e n z o J. L., F e r n á n d e z - L o p e z M. J.
Reinvigoration of mature Castanea sativa by serial micrografting onto juvenile clone //
Acta horticulturae. 2005. Vol. 693. P. 293–298.
9. G e b h a r d t K., G o l d b a c h H. Establishment, graft union characteristics
and growth of Prunus micrografts // Physiologia Plantarum. 1988. 72. P. 153–159.
10. K r a s i n s k a y a T. A., K u k h a r c h i k H. B. In vitro
micropropagation of various Cerasus Mill. Forms // Plodowodstwo. 2004. 16. P. 26–31.
11. L i t w i ñ c z u k W. Efficiency of a double-phase medium in micropropagation
of semi-dwarf apple rootstocks M.26, MM.106 and P 14 // Journal of Fruit and Ornamental
Plant Research. 2000. Vol. VIII., 3–4. P. 97–106.
12. L l o y d G., M c C o w n B. Commercially feasible micropropagation of
mountain laurel, Kalmia latifolia, by use of shoot tip culture // Intl Plant Prop Soc. Proc.
1980. 30. P. 421–427.
13. M n e n e y E. E., M a n t e l S. H. In vitro micrografting of cashew //
Plant Cell Tissue Organ Culture. 2001. 66(1). P. 49–58.
14. M u r a s h i g e T., S k o o g F. A revised medium for rapid growth and
bioassays with tobacco tissue cultures // Physiol Plant. 1962. 15. P. 473–497.
15. N a s M. N., R e a d P. E. Simultaneous micrografting, rooting and
acclimatization of micropropagated American chestnut, grapevine and hybrid hazelnut //
Europ. J. Hort. Sci. 2003. 68(5). P. 234–237.
16. Ö z z a m b a k E., S c h m i d t H. In vitro and in vivo micrografting of
cherry (Prunus avium L.) // Gartenbauwissenschaft. 1991. 56(5). P. 221–223.
17. P a t h i r a n a R., M c K e n z i e M. J. Early detection of grapevine leafroll
virus in Vitis vinifera using in vitro micrografting // Plant Cell Tissue Organ Culture. 2005.
81. P. 11—18.
18. S c h m i d t H., K e t z e l A., K e t z e l C., K ö p c k e K., R a d i e s
M., S c h u l z e M. Kirschfrüchte schon drei Jahre nach der Kreuzung? // Obstbau.
1997. 8. P. 410–412.
83
19. S t a r r a n t i n o A., C a r u s o A. The shoot-tip grafting technique applied
in viticulture // Acta horticulturae. 1998. Vol. 227. P. 101–103.
20. S e d l a k J., P a p r s t e i n F., E r b e n o v a M. In vitro propagation
of dwarfing sweet cherry rootstocks P-HL. 5th International Cherry Symposium, BursaTurkey // Book of abstracts. 2005. 31 p.
21. T a n n e E., S h l a m o v i t z N., S p i e g e l - R o y P. Rapidly
diagnosing grapevine corky-bark by in vitro micrografting // HortScience. 1993. 28(6).
P. 667—668.
22. W a n g Q. Shoot multiplication of pear in double–phase medium culture //
Acta horticulturae. 1991. Vol. 289. P. 349–350.
23. V i s e u r J. Micropropagation of pear, Pyrus communis L. in a double-phase
culture medium. // Acta horticulturae. 1987. Vol. 212. P. 117-–124.
24. P r o j e c t no 3 P06 R 0 58 25 supported by Ministry of Scientific Research and
Information Technology
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 77–84.
VEGETATYVINIAI VYÐNIØ POSKIEPIAI AUDINIØ KULTÛROJE
E. Dziedzic, M. Maùodobry
Santrauka
Trys vyðniø poskiepiai: PHL-6, PHL-84 ir F12/1, buvo dauginami kietoje ir dviejø
faziø terpëje pagal MS terpæ. Tirtas BA citokinino ir IBA bei NAA auksinø poveikis ûgliø
dauginimui. Terpëje, kurioje buvo IBA auksino, ûgliai buvo dauginami sëkmingiau negu
terpëje su NAA. Daugiau þaliosios masës pagausëjo dviejø faziø terpëje. Ûgliai ásiðaknijo
WPM terpëje, kurioje buvo IBA ir IAA auksinø. Tirti poskiepiai nesiskyrë ûgliø ilgiu,
ðaknø skaièiumi ir bendru ðaknø ilgiu, tenkanèiu vienam ûgliui. ‘Regina’ veislës
mikroskiepijimas á Damil ir Gisela 5 poskiepius bei ‘Van’ veislës – á poskiepá Damil buvo
atliktas skirtingais skiepijimo in vitro metodais. Áskiepijus ‘Regina’ ir ‘Van’ veisles á Damil
poskiepá, gautas didelis pavykusiø mikroskiepø procentas.
Reikðminiai þodþiai: vyðniø poskiepiai, mikroskiepijimas, ásiðaknijimas, dviejø faziø
terpë.
84
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 85–89.
PERFORMANCE OF SOME VEGETATIVELY
PROPAGATED APPLE ROOTSTOCKS IN THE NURSERY
Sava TABAKOV 1, Anton YORDANOV 2
Department of Fruit Growing Agricultural University – Plovdiv
12 Mendeleev str., 4000 Plovdiv, Bulgaria.
E-mails: [email protected]; [email protected]
Five apple rootstocks (M.9, M.26, J-TE-H, J-OH-A and J-TE-F) were studied in
commercial clonal stoolbed in 2003–2005. The rootstocks were planted in the autumn of
1999 at the density of 10,000 plants per hectare. The shoots developing from mother
plants were pruned in the stoolbed annually at the height of 10–15 cm above the ground.
First hilling up was done when stool shoots were 15–20 cm high, and the second one –
when stool shoots were 35–40 cm high. The aim of the study was to determine the yield of
stool shoots per plant and per hectare, mean diameter of stool shoots and their distribution
in five classes of quality (according to their thickness), height of stool shoots, number of
feathered stool shoots, mean number of roots per stool shoot. The yield of stool shoots
was the highest on rootstocks J-TE-F and M.26 and the smallest on M.9. The thickest
were stool shoots on M.9. The smallest number of feathered stool shoots was noted on
J-TE-F, and the best rooting was recorded on M.26.
Key words: apple, rooting, rootstocks, stoolbed, yield.
Introduction. Investigations of clonal apple rootstocks concern mainly maiden
trees or bearing orchards. Many researchers studied tree vigour, cropping efficiency
coefficient, fruit quality, etc. on different cultivar-rootstock combinations (Blaþek
1999; Hrotko et al. 1997; Ystaas et al., 1997; Kosina, 1991; Vercammen, 2004;
Kosina, 2004). The available literature about propagation and stoolbed properties of
rootstocks of J-TE-series is rather limited. As far as the Bulgarian conditions are
concerned, such information is not available at all. For this reason, it has been
attempted to investigate stoolbed properties of J-TE-H, J-OH-A, J-TE-F, along with
the widespread rootstocks M.9 and M.26.
Material and methods. Mother plants of rootstocks M.9, M.26, J-TE-H,
J-OH-A and J-TE-F were planted in the autumn of 1999 at the density of 10 000
plants per hectare. Since 2001 shoots developing from the mother plants were pruned
in stoolbed at the height of 10–15 cm above the ground (the upper halves of the
shoots were removed). This pruning increased the yield of stool shoots. First hilling
up was carried out when stool shoots were 15–20 cm high, and the second one –
85
when stool shoots were 35–40 cm high. The study was conducted during the period
of 2003–2005. The experiment was set up in a randomised block design, with 4
replications and 12 plants per plot. The following parameters were determined: yield
of stool shoots per plant and per hectare, mean diameter of stool shoots and their
distribution in five classes of quality (according to their thickness), height of stool
shoots, number of feathered stool shoots, mean number of root tufts per stool shoot.
Results and discussion. From 46 to 69 percent of the yield of stool shoots
were reckoned to the classes of 6–8 and 8–10 mm of diameter. The highest percentage
of shoots <6 mm was noted on J-OH-A. The highest percentage of shoots >12mm
(overgrown) was recorded on M.9 (Fig. 1-5).
F i g. 1. Distribution of the yield of stool shoots on M.9 in five classes of quality (%)
1
p a v.
M.9 atlankø derliaus pasiskirstymas á penkias kokybës klases, %
F i g. 2. Distribution of the yield of stool shoots on M.26 in five classes of quality (%)
2
p a v.
M.26 atlankø derliaus pasiskirstymas á penkias kokybës klases, %
The largest number of shoots in the class of 6–8 mm in diameter was recorded
on J-TE-F, but the difference was significant only in comparison with M.9
(Table 1). The largest number of shoots in the class of 8–10 mm was recorded on
J-TE-F, but the difference was significant only with M.9, J-OH-A and J-TE-H. No
significant differences were found in the classes of <6 mm and 10–12 mm.
86
F i g. 3. Distribution of the yield of stool shoots on J-TE-H in five classes of quality (%)
3
p a v.
J-TE-H atlankø derliaus pasiskirstymas á penkias kokybës klases, %
F i g. 4. Distribution of the yield of stool shoots on J-OH-A in five classes of quality (%)
4
p a v.
J-OH-A atlankø derliaus pasiskirstymas á penkias kokybës klases, %
F i g. 5. Distribution of the yield of stool shoots on J-TE-F in five classes of quality (%)
5
p a v. J-TE-F atlankø derliaus pasiskirstymas á penkias kokybës klases, %
The largest number of root tufts per shoot was recorded on M.26 (Table 2).
Considering this parameter, it was found that M.26 significantly surpassed J-TE-H,
M.9 and J-OH-A, which had the smallest number of root tufts per shoot. J-TE-F did
not differ significantly in respect to this trait. The smallest number of feathered stool
shoots was noted on J-TE-F, and the largest number of feathered shoots was recorded
on M.26 and M.9. The other rootstocks showed the intermediate values of this trait.
The thickest were the stool shoots of M.9, the differences from the other rootstocks
tested was significant. Regarding the total number of stool shoots per mother plant
87
no significant differences were noted among the rootstocks. The most productive
rootstock per mother plant and per hectare was J-TE-F, followed by M.26. The
least productive were M.9 and J-OH-A, J-TE-H having occupied an intermediate
position. M.26 and M.9 had the highest shoots, whereas the shoots of J-OH-A were
the shortest.
T a b l e 1. Mean number of stool shoots according to their diameter
1
l e n t e l ë. Ávairaus skersmens atlankø vidutinis skaièius
Diameter / Skersmuo, mm
Rootstock
Poskiepis
<6
6–8
8–10
10–12
>12
Ì.9
Ì.26
J-TE-H
J-OH-A
J-TE-F
7.1
8.7
8.0
10.9
11.8
11.0
20.8
16.0
16.6
20.9
11.7
19.4
15.1
12.9
25.8
9.6
10.5
12.0
8.1
8.1
9.7
3.9
4.6
3.0
1.4
LSD05/R05
LSD05/R05
LSD05/R05
6.63
9.30
13.14
7.22
10.12
14.30
9.94
13.94
19.70
4.63
6.49
9.18
3.03
4.25
6.01
T a b l e 2. Growth characteristics of different rootstocks
2
l e n t e l ë. Skirtingø poskiepiø augimo charakteristikos
Total number of
Mean number Mean number
stool shoots per Mean diameter Mean height of of feathered of root tufts per
Rootstock mother plant 1 of stool shoot
a stool shoot
stool shoots
stool shoot
Poskiepis Bendras motininio Vidutinis atlankos Vidutinis atlankos
Vidutinis
Vidutinis ðaknø
skersmuo
aukštis,
,
mm
cm
augalo atlankø
suðakojusiø
skaièius
1
atlankø skaièius
skaièius
Ì.9
Ì.26
J-TE-H
J-OH-A
J-TE-F
49.3
63.3
55.8
51.5
67.9
10.1
8.3
8.6
8.4
8.2
72
74
63
53
60
5.5
5.7
4.6
3.2
1.8
4.0
5.3
3.9
4.5
4.6
LSD05/R05
LSD05/R05
LSD05/R05
17.38
24.37
31.45
0.89
1.25
1.77
5.3
7.4
10.4
1.84
2.58
3.65
0.79
1.11
1.57
for the period of 2003–2005 / 2003–005 m. laikotarpis
Conclusions. M.26 has the best rooting habit. J-TE-F shows the smallest number
of feathered stool shoots. The largest number of overgrown (thicker than 12 mm)
stool shoots is a characteristic of M.9. The highest yield of stool shoots may be
obtained from J-TE-F or M.26 and the smallest from M.9.
Gauta
2006 05 24
Parengta spausdinti
2006 07 13
88
References
1. B l a þ e k J. Performance of EW rootstocks in intensive apple orchards in the
Czech Republic // Apple rootstocks for intensive orchards. Proceedings of the International
Seminar. Warsaw-Ursynów, Poland, August 18–21, 1999. P. 19-20.
2. D v o ø a k A. Breeding of rootstocks J-TE and their influence on growth and
productivity of different cultivars // Acta Horticulturae. 1988. Vol. 224. P. 325-330.
3. H a n s e n O. B. The rooting potential of dwarfing apple rootstocks // NorskLandbruksforsking. 1990. 4. 2. P. 73-79.
4. H r o t k o K., M a g y a r L., H a n u s z B. Apple rootstock trials at the
Faculty of Horticulture, UHF Budapest (Preliminary report) // Acta Horticulturae. 1997.
Vol. 451. P. 153-159.
5. K o s i n a J. Effect of rootstocks on growth, productivity and fruit quality of
apples at the onset of fertility // Zahradnictvi-UVTIZ (CSFR). 1991. Vol. 18(2). P. 83-92.
6. K o s i n a J. Growth and yield of apples on new Czech dwarfing rootstocks //
Acta Horticulturae. 2004. Vol. 663. P. 945-948.
7. M a n t i n g e r H. Eine Neue Apfel-unterlagenserie aus der Tschechei //
Obstbau-Wienbau. 1996. 33(10). P. 255-256.
8. V e r c a m m e n J. Search for a more dwarfing rootstock for apple // Acta
Horticulturae. 2004. Vol. 658. P. 313-318.
9. Y s t a a s J., F r ø y n e s O., M e l a n d M. Evaluation of 9 apple
rootstocks the first cropping year in a Northern climate // Acta Horticulturae. 1997. Vol.
451. P. 147-152.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 85–89.
KAI KURIØ MEDELYNE VEGETATYVINIU BÛDU DAUGINAMØ OBELØ
POSKIEPIØ APIBÛDINIMAS
S. Tabakov, A. Yordanov
Santrauka
2003–2005 metais komerciniame vegetatyviniame daigyne tirti penki obelø poskiepiai
(M.9, M.26, J-TE-H, J-OH-A ir J-TE-F). Jie buvo pasodinti 1999 metø rudená po 10 tûkst. á
hektarà. Motininiø augalø atþalos augyne kasmet buvo apgenimos 10–15 cm atstumu nuo
þemës pavirðiaus. Pirmàjá kartà buvo apkaupta atþaloms esant 15-20 cm, antràjá – 35–40 cm
aukðèio. Tyrimo tikslas – nustatyti atlankø derliø, tenkantá kiekvienam augalui ir hektarui,
vidutiná atlankø skersmená ir jø pasiskirstymà á penkias kokybës klases (pagal storumà),
atlankø aukðtá, iðsiðakojusiø atlankø skaièiø, vidutiná kiekvienos atþalos ðaknø skaièiø.
Didþiausià derliø davë J-TE-F ir M.26, maþiausià – M.9 poskiepiø atþalos. Storiausios
buvo M.9 poskiepio atþalos. Maþiausiai iðsiðakojusiø atlankø buvo ant J-TE-F, geriausiai
ásiðaknijo M.26 poskiepio atþalos.
Reikðminiai þodþiai: obelys, ásiðaknijimas, poskiepiai, augynas, derlius.
89
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 90–97.
YIELDING OF APPLE TREE CVS. ‘FIESTA’ AND ‘PINOVA’
DEPENDING ON THE AGE OF PLANTING MATERIAL
AND METHODS OF ITS PRODUCTION IN A NURSERY
Ewelina GUDAROWSKA, Adam SZEWCZUK,
Department of Horticulture, University of Agriculture, Rozbrat 7,
50-334 Wrocùaw, Poland. E-mail: [email protected]
In the spring of 2002 one-year-old and two-year-old apple tree cvs. ‘Fiesta’ and
‘Pinova’, budded on M.26 rootstock, were planted at the distances of 3.5 x 1.0 m. The
planting material was produced in a nursery using chemicals (Arbolin 036 SL, Arbostim
100 SL), pinching and pruning at the height of 100 cm. Those agrotechnical practices were
applied in the 3rd (for knip-boom trees) and 2nd (for maiden trees) year of production in
nursery. Two-year-old trees were not pruned after planting. Some of one-year-old trees in
control treatment were additionally pruned at the height of 40 cm, 60 cm, 80 cm and 100 cm
after planting.
The highest total yield was obtained from ‘Pinova’, planted as knip-boom trees,
produced in a nursery by methods, which stimulate feathering. In the case of maiden
trees, high yield was noted for control trees and sprayed with Arbolin 036 SL. For ‘Fiesta’
two-year-old material had more flowers in the first two years after planting. However, the
use of chemicals in a nursery had positive effect on the yield in the case of maiden trees.
The lowest yields were obtained from maiden trees pruned at the height of 40 cm and
60 cm (‘Pinova’) and 80 cm (‘Fiesta’) after planting.
Key words: age of planting material, apple trees, methods of tree production, tree
training, yield.
Introduction. The feathering of young trees is an important factor inducting
early fruit production. One-year-old trees without branches need at least one year to
produce crown (Bielicki, Czyczyk, 2004 b). The main factor determining branching
is cultivar (Basak et al., 1994). Several well-known apple cultivars (‘Ligol’, ‘Alwa’,
‘Gloster’) produce laterals in insufficient number (Gudarowska, 2002). Traditional
techniques to promote branching not always give satisfactory results, so application
of bioregulators may be necessary (Csiszár, Bubán, 2004). Benzyladenine is applied
very often for training canopies of planting material (Basak et al., 1994; Hrotko et al.
1996). Benzyloadenine in combinations with gibberellins are also used to overcome
apical dominance and to stimulate feathering (Gàstoù, Poniedziaùek, 2004; Jaumieñ et
al., 2002). Such chemicals as Arbolin 036 SL can be use as well in nursery for
90
production of two-year-old trees (Gudarowska, Szewczuk, 2002).
However, bioregulators may have different influence on initiation of blossoming
(Gudarowska, Szewczuk, 2004 a). In the case of gibberellins, the possible role of
these hormones in flower initiation is discussed. According to Basak (2001), the
spray with gibberellins (GA3) could reduce flower initiation of fruiting trees. Jaumieñ
(1999) introduces results of experiments, which were carried out in Great Britain
and New Zealand ant show diverse influence on form of bud flowers.
According to Bielicki and Czynczyk (2004 a), heading back one-year-old trees
at the height of 65 cm above the ground level produced high quality of knip-boom
with the most shoots longer than 30 cm. In Gudarowska and Szewczuk (2004 b)
experiment, the pruning height at 60 cm and 100 cm in nursery, positively affected
the blossoming of young apple trees in the orchard.
Materials and methods. The experiment was carried out in the nursery in
2001 and in the orchard in 2002-2005. In the spring of 2002 one-year-old and twoyear-old apple tree cvs. ‘Fiesta’ and ‘Pinova’ on M.26 rootstock were planted at a
spacing of 3.5 x 1.0 m. The trees originated from nursery where as one-year-old
material, in the spring of the 3rd year of nursery production they were pruned at the
height of 60 cm and 100 cm above the ground level. At the beginning of July oneyear-old and two-year-old trees pruned at 60 cm, were treated as follows: pinching
(below the 2nd leaf) and spraying with Arbolin 036SL and Arbostim 100SL. Arbolin
036 SL containing 18mg gibberellins (GA3) and 18 mg benzyladenine (BA) in 1 l of
agent was applied once in dose 25 ml/1l of water. Arbostim 100 SL contains 100 g
gibberellins in 1 l of agent applied one in dose 5 ml/1l of water. After planting into the
orchard two-year-old trees and part of maiden trees were not pruned, another part
of maiden trees was pruned at the height of 40 cm, 60 cm, 80 cm, and 100 cm.
The inflorescences and yield were recorded of each tree. In the first year of
planting all flowers were removed after counting. The experiment was carried out in
a randomised block design in 5 replications. Each experimental plot consisted of
4 trees. The obtained results were statistically processed by analysis of variance.
The significance of differences between means was evaluated by T-Duncan’s multiple
range test at P=0.05
Results. During the first three years after planting there was noted the most
intensive blossoming of two-year-old trees ‘Pinova’ (Table1). Pinching and spraying
with chemicals reduced blossoming of two-year-old trees as well as maiden trees of
cv. ‘Pinova’ In the case of maiden trees, pruning at the height of 40 cm, 60 cm, and
80 cm also affected less number of flowers. The highest total yield in 2003-2005
was obtained from cv. ‘Pinova’, planted as two-year-old material pruned in a nursery
at the height of 100 cm and 60 cm and additionally by using of methods stimulating
feathering (18.3-19.7 kg per tree). In the case of maiden trees, high yield was noted
for control trees (19.2 kg per tree) and sprayed Arbolin 036 SL – 17.8 kg per tree
(Table 3).
Two-year-old material of cv. ‘Fiesta’ had more flowers during the first two
years after planting into the orchard. However, Arbolin 036 SL reduced the number
of flowers in the first year (Table 2). In the 3rd year after planting, the number of
inflorescences from trees planted as knip-boom and maiden material, and additionally
91
pinched and sprayed with chemicals, were comparable (Table 2). Despite of the
initial differences of blossoming intensity, the significantly lowest cumulative yield
was obtained from ‘Fiesta’ planted as maiden trees and pruned after planting at the
height of 40 cm and 80 cm (Table 4).
T a b l e 1. The influence of age and methods of planting material
production on the number of inflorescences on apple tree
cv. ‘Pinova’ during the first three years after planting
1
l e n t e l ë. Sodinukø amþiaus ir dauginimo bûdø átaka ‘Pinova’ veislës obelø
þiedynø skaièiui pirmuosius trejus metus po pasodinimo
Number of inflorescences / Þiedynø skaièius
2002
2003
2004
Two-year-old trees / Dvejø metø vaismedþiai
Control 60 cm / Kontrolë 60 cm
14.5 e*
10.4 bcd
98.9 de
Control 100 cm / Kontrolë 100 cm
35.3 f
16.5 de
106.0 de
Pinching / Pinciravimas
5.0 abc
35.1 g
110.0 de
Arbolin
6.9 bcd
31.2 g
127.6 f
Arbostim
8.5 cd
28.8 fg
87.6 cd
One-year-old trees / Vieneriø metø vaismedþiai
Control / Kontrolë
10.4 d
21.1 ef
65.0 b
Pinching / Pinciravimas
1.7 a
12.2 cde
69.5 bc
Arbolin
1.4 a
17.6 de
68.5 bc
Arbostim
4.8 abc
20.4 ef
66.6 bc
One-year-old trees after planting / Vieneriø metø vaismedþiai po pasodinimo
40 cm
3.7 ab
0.3 a
32.4 a
60 cm
3.5 ab
1.0 ab
23.5 a
80 cm
3.5 ab
11.8 cde
73.1 bc
100 cm
7.6 cd
3.1 abc
32.5 a
Treatment
Variantas
* Means within a column marked with the same letter do not differ significantly at p=0.05
according to Duncan’s multiple range test.
* Tarp ta paèia raide paþymëtø reikðmiø skiltyse pagal Dunkano kriterijø esminiø skirtumø
nëra (p=0,05).
Discussion. The obtained results showed that age and method of planting
material production affected the bud formation and yield of apple trees. But the
observed reaction depended on cultivar (Tables 1-4). Using two-year-old planting
material positively affected the yield. These results confirmed earlier reports, which
were presented by Bielicki and Czynczyk (2004 a, b).
However, the use of chemicals containing plant hormones for maiden trees in
nursery had similar influence on the yielding in orchard. It was clearly visible for
cultivar ‘Fiesta’ (Tables 2, 4). For cultivar with tendency to the spontaneous feathering
and blossoming in the year of planting, such as ‘Pinova’, agents containing cytokinins
in combination with gibberellins could reduce number of inflorescences in the first
year. This is important for cultivars, which after blossoming and fruiting in the first
year could start biennial yielding (Gudarowska, Szewczuk, 2004 a, b).
92
T a b l e 2. The influence of age and methods of planting material
production on the number of inflorescences on apple tree
cv. ‘Fiesta’ during the first tree years after planting
2
l e n t e l ë.
Sodinukø amþiaus ir dauginimo bûdø átaka ‘Fiesta’ veislës obelø
þiedynø skaièiui pirmuosius trejus metus po pasodinimo
Number of inflorescences / Þiedynø skaièius
Treatment
Variantas
2002
2003
2004
Two-year-old trees / Dvejø metø vaismedþiai
Control 60 cm / Kontrolë 60 cm
6.5 bcd
8.3 c
66.8 d
Control 100 cm / Kontrolë 100 cm
6.8 cd
15.0 d
33.8 ab
4.6 abcd
5.5 abc
61.2 cd
Arbolin
2.7 ab
14.6 d
63.5 cd
Arbostim
8.1 d
6.8 bc
62.3 cd
Pinching / Pinciravimas
One-year-old trees / Vieneriø metø vaismedþiai
Control / Kontrolë
1.1 a
5.5 abc
39.6 abc
Pinching / Pinciravimas
2.7 ab
6.8 bc
61.6 cd
Arbolin
3.3 abc
6.9 bc
61.0 cd
Arbostim
2.8 abc
5.4 abc
51.2 bcd
One-year-old trees after planting / Vieneriø metø vaismedþiai po pasodinimo
40 cm
1.2 a
0a
23.4 a
60 cm
0.7 a
0.4 a
23.0 a
80 cm
1.1 a
2.0 a
42.4 abcd
100 cm
0.8 a
3.8 abc
48.0 abcd
For explanation see Table 1 / Paaiðkinimus þr. 1 lentelëje
According to Mika (1997), the pruning of young trees can reduce number of
flower buds. This opinion was confirmed in present study, first of all for trees
pruned at the height of 40 cm and 60 cm in the case of ‘Pinova’ and at 80 cm in the
case of ‘Fiesta’ (Table 4). On the other hand, strong, well-branched planting material
should be planted only in very good soil (Bielicki, Czynczyk, 2004a). In bad soil
conditions, pruning one-and two-year-old trees after planting should be necessary.
The obtained preliminary results point at necessity to adapt the nursery technique
to genetic features of cultivar and the methods of training of the trees after planting
into an orchard.
93
T a b l e 3. The yield of apple tree cv. ‘Pinova’ on M.26 depending on
the age and methods of planting material production
3
l e n t e l ë. ‘Pinova’ veislës obelø su M.26 poskiepiu derliaus priklausomumas
nuo sodinukø amþiaus ir dauginimo bûdø
Yield, kg/tree / Derlius, kg/medis
Treatment
Variantas
2003
2004
2005
Total yield in
2003–2005, kg/tree
Suminis derlius
2003–2005 m., kg/medis
Two-year-old trees / Dvejø metø vaismedþiai
Control 60 cm / Kontrolë 60 cm
0.7 b
8.1 def
7.7 def
16.5 cde
Control 100 cm / Kontrolë 100 cm
1.5 de
9.1 f
8.5 efg
19.1 f
Pinching / Pinciravimas
1.7 e
8.6 ef
9.4 fg
19.7 f
Arbolin
0.9 bc
9.0 f
8.4 defg
18.3 ef
Arbostim
1.2 cd
8.2 def
9.1 fg
18.5 ef
One-year-old trees / Vieneriø metø vaismedþiai
Control / Kontrolë
1.7 e
7.5 cde
10.0 g
19.2 f
Pinching / Pinciravimas
1.0 bc
7.0 cd
7.3 cde
15.3 c
Arbolin
1.2 cd
7.2 cd
9.4 fg
17.8 def
Arbostim
1.3 cde
6.7 bc
6.7 bcd
14.7 c
One-year-old trees after planting / Vieneriø metø vaismedþiai po pasodinimo
40 cm
0a
3.9 a
5.5 a
9.4 a
60 cm
0.2 a
2.9 a
4.4 a
7.5 a
80 cm
1.0 bc
7.6 cde
6.9 bcde
15.7 cd
100 cm
0.2 a
5.6 b
5.6 abc
11.4 b
For explanation see Table 1 / Paaiðkinimus þr. 1 lentelëje
94
T a b l e 4. The yield of apple tree cv. ‘Fiesta’ on M.26 depending on
the age and methods of planting material production
4
l e n t e l ë.
‘Fiesta’ veislës obelø su M.26 poskiepiu derliaus priklausomumas
nuo sodinukø amþiaus ir dauginimo bûdø
Yield, kg/tree / Derlius, kg/medis
Treatment
Apdorojimas
2003
2004
2005
Total yield in
2003–2005, kg/tree
Suminis derlius
2003–2005 m., kg/medis
Two-year-old trees / Dvejø metø vaismedþiai
Control 60 cm / Kontrolë 60 cm
1.3 e
10.0 e
4.1 abc
14.4 de
Control 100 cm / Kontrolë 100 cm
1.8 f
7.1 cd
4.2 abc
13.1 cde
Pinching / Pinciravimas
0.7 bcd
8.1 de
3.5 ab
12.2 bcd
Arbolin
1.1 de
6.4 cd
4.0 abc
11.5 abcd
Arbostim
0.8 cd
6.9 cd
2.5 a
10.2 abc
One-year-old trees / Vieneriø metø vaismedþiai
Control / Kontrolë
0.6 bc
4.5 abc
4.8 abc
9.9 ab
Pinching / Pinciravimas
0.6 bc
7.9 de
7.5 de
16.0 e
Arbolin
0.8 cd
7.5 de
4.6 abc
12.9 bcde
Arbostim
0.6 bc
6.4 cd
5.4 bcd
12.4 bcd
One-year-old trees pruned after planting / Vieneriø metø vaismedþiai po pasodinimo
40 cm
0a
2.7 a
6.0 cd
8.7 a
60 cm
0a
3.2 ab
9.3 e
12.5 bcd
80 cm
0.3 ab
5.6 bcd
3.1 ab
9.0 a
100 cm
0.5 bc
5.8 bcd
7.2 de
13.5 de
For explanation see Table 1 / Paaiðkinimus þr. 1 lentelëje
Conclusions. 1. The age of plant material and methods used for improving
feathering had an influence on the intensity of the blossoming and on the yielding of
apple tree cvs. ‘Pinova’ and ‘Fiesta’.
2. The high cumulative yield of cv. ‘Pinova’ was obtained from two-year-old
trees pruned in a nursery at the height of 100 cm and 60 cm and additionally pinched
and sprayed with chemicals.
3. Chemicals and pinching of young trees in a nursery positively affected the
yield obtained from trees planted as maiden plant material.
4. For both cultivars, the lowest total yields were obtained from maiden trees
pruned after planting at the height of 40 cm and 60 cm (‘Pinova’) and 80 cm (‘Fiesta’).
Gauta
2006 05 04
Parengta spausdinti
2006 07 13
95
References
1. B a s a k A. Kwas giberelinowy w sadownictwie. Sad Nowoczesny. 2001. 11.
P. 10-11.
2. B a s a k A., K o ù o d z i e j c z a k P., B u b á n T., U r f i n é F. É.
Paturyl 10 WSC as branching agent of young apple trees // Hort. Science. 1994. 26(2).
P. 46-49.
3. B i e l i c k i P., C z y n c z y k A. Effect of rootstock quality and height of
heading back one-year-old grafts on the quality of two-year-old trees in nursery // Journal
of Fruit and Ornamental Plant Research. 2004 a. Vol. 12. P. 61-67.
4. B i e l i c k i P., C z y n c z y k A. Influence of plant material quality on growth
and yield of two apple cultivars // Scientific Works of the Lithuanian Institute of
Horticulture and Lithuanian University of Agriculture. 2004 b. 21(4). P. 33-38.
5. C s i s z á r L., B u b á n T. Improving the feathering of young apple trees in
environment friendly way by modified benzyladenine application // Journal of Fruit and
Ornamental Plant Research. 2004. Vol. 12. P. 31-38.
6. G à s t o ù M., P o n i e d z i a ù e k W. Wpùyw róýnych preparatów
chemicznych na rozgaùæzianie okulantów jabùoni w szkóùce // Folia Univ. Agric. Stein,
Agricultura. 2004. 240(96). P. 65-68.
7. G u d a r o w s k a E. Wpùyw wysokoúci przyciæcia jednorocznych okulantów
piæciu odmian jabùoni na jakoýã otrzymanych drzewek dwuletnich // Zeszyty Naukowe
Instytutu Sadownictwa i Kwiaciarstwa. Skierniewice. 2002. T. 10. P. 75-82.
8. G u d a r o w s k a
E.,
Szewczuk
A. Wpùyw czynników
agrotechnicznych i bioregulatorów na stopieñ rozgaùæzienia jednorocznych i dwuletnich
drzewek jabùoni odmian ‘Gala’ i ‘Alwa’ na podkùadce M 26 // Zeszyty Naukowe Instytutu
Sadownictwa i Kwiaciarstwa. Skierniewice. 2002. T. 10. P. 29-37.
9. G u d a r o w s k a E., S z e w c z u k A. The influence of agro-technical
methods used in the nursery on quality of planting material and precocity of bearing in
young apple orchard // Journal of Fruit and Ornamental Plant Research. 2004 a. Vol. 12.
P. 91-96.
10. G u d a r o w s k a E., S z e w c z u k A. Wpùyw wysokoúci przyciæcia
okulantów w szkóùce na kwitnienie i owocowanie trzech odmian jabùoni w sadzie // Zeszyty
Naukowe Instytutu Sadownictwa i Kwiaciarstwa. Skierniewice. 2004 b. T. 12. P. 43-49.
11. H r o t k ó K., M a g y a r L., B u b á n T. Improved feathering by
benzyladenine application on one-year-old Idared apple trees In the nursery // Hort.
Science. 1996. 28(3-4). P. 49-53.
12. J a u m i e ñ F., D z i u b a n R., N o w a k o w s k i R. Arbolin extra – a
new promising chemical for branching apple trees in nurseries // Scientific Works of the
Lithuanian Institute of Hort. and Lithuanian University of Agriculture. 2002. 21(2). P. 106-116.
13. J a u m i e ñ F. Wpùyw giberelin na tworzenie siæ pàków kwiatowych u drzew
owocowych. Ogrodnictwo. 1999. 1. P. 6-8.
14. M i k a A. Nowe kierunki zakùadania i prowadzenia sadów // Ogrodnictwa.
1997. 5. P. 10-13.
96
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 90–97.
OBELØ VEISLIØ ‘FIESTA’ IR ‘PINOVA’ DERLIAUS PRIKLAUSOMUMAS
NUO SODINUKØ AMÞIAUS IR DAUGINIMO BÛDØ
E. Gudarowska, A. Szewczuk
Santrauka
2002 m. pavasará vieneriø ir dvejø metø ‘Fiesta’ ir ‘Pinova’ veisliø obelys su M.26
poskiepiu buvo pasodintos 3,5 x 1,0 m atstumais. Sodinukai buvo iðauginti medelyne
naudojat cheminius preparatus (Arbolin 036 SL, Arbostim 100 SL), pinciruojant ir genint
100 cm aukðtyje. Ðios agrotechninës priemonës buvo taikytos treèiaisiais (dvimeèiams su
vienameèiu vainiku) ir antraisiais dauginimo medelyne metais. Dvejø metø vaismedþiai po
pasodinimo genimi nebuvo. Kai kurie kontrolinio varianto vieneriø metø vaismedþiai buvo
papildomai patrumpinti 40, 60, 80 ir 100 cm aukðtyje.
Didþiausià suminá derliø davë dvimetës su vienameèiu vainiku ‘Pinova’ veislës obelys,
iðaugintos medelyne taikant ðakojimàsi stimuliuojanèius metodus. Auginant vienameèius
sodinukus, didelá derliø davë kontrolinio varianto ir Arbolin 036 SL apipurkðti vaismedþiai.
Dvimeèiai ‘Fiesta’ veislës sodinukai pirmuosius dvejus metus po pasodinimo sukrovë
daugiau þiedø. Cheminiø preparatø naudojimas medelyne turëjo teigiamos átakos sodinukø
derliui. Maþiausià derliø davë sodinukai, po pasodinimo patrumpinti 40 ir 60 cm aukðtyje
(‘Pinova’) ir 80 cm aukðtyje (‘Fiesta’).
Reikðminiai þodþiai: sodinukø amþius, obelys, vaismedþiø dauginimas, vaismedþiø
formavimas, derlius.
97
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 98–103.
THE INFLUENCE OF THE HEIGHT OF PRUNING OF
APPLE TREES IN A NURSERY ON THEIR QUALITY
AND YIELDING
Ewelina GUDAROWSKA, Adam SZEWCZUK, Dariusz DEREÑ
Department of Horticulture, University of Agriculture, Rozbrat 7,
50-334 Wrocùaw, Poland. E-mail: [email protected]
The experiment was carried out in a nursery in 2001 and then in an orchard in 20022005. Maiden trees of cvs. ‘Ligol’ and ‘Alwa’ on M.26 rootstock were pruned at the height
of 40 cm, 60 cm, 80 cm and 100 cm above the soil level in the 3nd year of production in the
nursery. In the autumn of 2001, the quality of two-year-old planting material was estimated.
For both cultivars, the highest trees with the biggest diameter were obtained after
pruning at the height of 100 cm. In the case of cv. ‘Ligol’, pruning at 40 cm and 100 cm
stimulated branching. For cv. ‘Alwa’, pruning only at the height of 100 cm positively
affected the number of shoots.
In the spring of 2002, the trees were planted into the orchard, 3,5 x 1,0 m apart. In
2002-2004 the number of inflorescences and yield (2003–2005) from each tree were estimated.
The trees pruned at 100 cm in the nursery, had the highest number of inflorescences
in the year of planting. In the orchard cv. ‘Ligol’ was more productive (22 kg/tree) than
‘Alwa’ (13 kg/tree) in 2003–2005. The height of pruning at 60 cm and 100 cm in the nursery,
positively affected the yield of ‘Ligol’ and ‘Alwa’ (12.9–24.7 kg/tree), in comparison with
those pruned at the height of 40 cm and 80 cm (11.6–19.7 kg /tree).
Key words: apple tree, height of pruning, inflorescences, planting material quality,
yielding.
Introduction. The quality of planting material significantly affected the yield of
trees in an orchard. Strong planting material with a few shoots guarantees early and
high cropping (Van Oosten, 1978; Green, 1991). Two-year-old trees with one-year
old crowns are perfectly suited to the needs of modern 21st century fruit production
because they start bearing early and produce higher yields, especially in the first two
years after planting (Bielicki i Czynczyk, 1999) .
The main factor determining branching is genetics. Lateral shoots formation
depends on the apical dominance of the variety (Wertheim, 1978). Other important
factors in sylleptic branch formation are: rootstock, environmental conditions and
growing method (Bielicki i Czynczyk, 2004; Wertheim, 1978). According to Czarnecki
(1998) and Bielicki and Czynczyk (2000), heading back maiden trees of cvs. ‘Lobo’
and ‘Jonagold’ 65 cm above the ground level produced high quality two-year-old
98
trees with one-year-old crowns. Similar results were obtained by Gudarowska (2002)
for five other cultivars. The result obtained later in the orchard showed that the
pruning at the height of 60 cm and 100 cm in a nursery positively affected the
blossoming of young apple trees in the orchard (Gudarowska, Szewczuk, 2004).
The aim of the present study was to estimate the influence of the pruning height
of maiden trees in a nursery on the quality of produced two-year-old trees and their
yield potential during first four years after planting in an orchard.
Materials and methods. The first part of this experiment was carried out in a
nursery in 2001. In the spring of the 3rd year of planting, maiden trees of cvs. ‘Ligol’
and ‘Alwa’ on M.26 rootstock were pruned at the height of 40 cm, 60 cm, 80 cm
and 100 cm above the soil level. In the autumn of 2001, the quality of two-year-old
planting material was estimated on the basis of their diameter, height and branching.
In the second part of the experiment, the estimated two-year-old trees with
one-year-old crown were planted into the orchard in the spring of 2002, at a spacing
of 3.5 x 1.0 m. The trees were not pruned after planting. In the year of planting all
flowers were removed after counting. The number of inflorescences and yield were
noted for each tree.
The experiments were established in a randomised block design: in a nursery –
in 3 replications with 10 trees per plot, in the orchard – in 4 replications with 4 trees
per plot. The obtained results were statistically processed by an analysis of variance.
The significance of differences between means was evaluated according to
T-Duncan’s multiple range test at P=0.05.
Results. The pruning height of maiden trees in nursery had a significant influence
on the quality of two-year-old apple trees after the 3rd year of production (Table 1).
First of all, the height of pruning affected the height of trees and the number of
shoots > 20 cm long. The strongest trees were obtained after pruning at the height
of 100 cm above the soil level. For both cultivars pruning at 100 cm improved the
feathering of trees, their diameter and height. The obtained results were more significant
for cultivar ‘Ligol’ than for ‘Alwa’. In the case of ‘Ligol’, pruning at the height of
80 cm positively affected the height of planting material. However, pruning at the
height of 40 and 60 cm improved the feathering of trees.
The diverse quality of planting material affected the blossoming and yielding of
young trees in the orchard (Table 2). Stronger two-year-old apple trees of cv. ‘Ligol’
with well branched one-year-old crown had more inflorescences in the first year
after planting. In the next year (2004), no differences in ‘Ligol’ blossoming were
noted. However, the highest total yield in 2003-2005 was obtained from cv. ‘Ligol’
pruned in the nursery at the height of 60 cm and 100 cm (Table 3).
In the first two years after planting, more inflorescences were noted for trees
of cv. ‘Alwa’ when higher trees pruned at the height of 80 cm and 100 cm. In the
next year more inflorescences had trees pruned at the height of 40 cm, 60 cm and
100 cm (Table 2). The total yield in 2003–2005 was obtained from trees of cv.
‘Alwa’ pruned at the height of 60 and 100 cm (Table 3).
99
T a b l e 1. The influence of the pruning height of maiden trees in a
nursery on the quality of two-year-old apple trees
1
l e n t e l ë.
Height of
pruning
Trumpinimo
aukštis
40 cm
60 cm
80 cm
100 cm
40 cm
60 cm
80 cm
100 cm
Sodinukø medelyne trumpinimo aukðèio átaka dvimeèiø obelø
kokybei
Height
Diameter
Skersmuo,
mm
Aukštis,
16.1 a*
15.8 a
14.9 a
17.8 b
120.9 a
140.3 b
159.8 c
203.1 d
154.5 a
170.7 a
191.2 b
215.5 c
16.0 a
16.4 a
16.2 a
17.7 a
mm
Number of shoots >
20 cm long
Total length of
shoots
Ilgesniø kaip 20 cm
ûgliø skaièius
Bendras ûgliø
ilgis, cm
‘Ligol’
2.2 ab
2.1 ab
0.2 a
3.6 b
2.7 bc
2.3 b
0.6 a
7.4 c
96.9 a
82.6 a
30.3 a
345.3 b
‘Alwa’
0a
0a
0a
5.0 b
0.2 a
0a
0.1 a
4.9 b
9.1 a
0a
8.4 a
311.7 b
Number of shoots
< 20 cm long
Trumpesniø kaip 20
cm ûgliø skaièius
*Means within the columns marked with the same letter do not differ significantly at p=0.05,
according to Duncan’s multiple range test.
* Tarp ta paèia raide paþymëtø reikðmiø skiltyse pagal Dunkano kriterijø esminiø skirtumø
nëra (p=0,05).
T a b l e 2. The influence of the pruning height of maiden trees in a
nursery on the number of inflorescences during the first
three years after planting in an orchard
2
l e n t e l ë. Sodinukø medelyne trumpinimo aukðèio átaka þiedynø skaièiui
pirmuosius trejus metus po pasodinimo sode
Number of inflorescences / Þiedynø skaièius
Height of pruning
Trumpinimo aukštis
2002
2003
2004
40 cm
60 cm
80 cm
100 cm
5.0 a
9.3 ab
6.2 a
12.9 b
‘Ligol’
7.9 ab
7.1 a
5.9 a
9.3 b
30.5 a
49.4 a
21.6 a
36.9 a
40 cm
60 cm
80 cm
100 cm
0.07 a
0.06 a
0.12 a
2.82 b
‘Alwa’
4.2 a
5.7 a
12.7 b
9.2 ab
For explanation see Table 1 / Paaiðkinimus þr. 1 lentelëje
100
21.4 ab
26.0 b
13.4 a
19.5 ab
T a b l e 3. The yielding of apple tree cvs. ‘Ligol’ and ‘Alwa’ on M.26
depending on the pruning height of the trees in a nursery
3
l e n t e l ë. ‘Ligol’ ir ‘Alwa’ veisliø obelø su M.26 poskiepiu derliaus
priklausomumas nuo vaismedþiø trumpinimo aukðèio medelyne
Yield, kg/tree
Height of
pruning
Trumpinimo
aukštis
40 cm
60 cm
80 cm
100 cm
40 cm
60 cm
80 cm
100 cm
Total yield, kg/tree
2003–2005
Derlius, kg/medis
2003
2.3 ab
1.6 a
1.5 a
2.5 b
0.5 a
0.5 a
1.5 b
1.0 ab
2005
2004
8.1 a
12.6 b
7.2 a
10.3 b
3.6 ab
5.0 b
2.5 a
3.8 ab
Suminis derlius
2003–2005 m., kg/medis
Mean fruit weight
2003–2005
Vidutinë vaisiø masë
2003–2005 m., g
‘Ligol’
9.3 a
9.4 a
11.4 a
11.9 a
19.7 a
23.6 b
20.1 a
24.7 b
195 a
190 a
195 a
195 a
‘Alwa’
6.5 a
9.7 a
7.7 a
8.1 a
11.6 a
15.2 b
11.7 a
12.9 ab
116 a
120 a
117 a
115 a
For explanation see Table 1 / Paaiðkinimus þr. 1 lentelëje
Discussion. One of the factors affecting early production is the quality of planting
material (Green, 1991; Van Osten, 1978). Apple trees of cv. ‘Ligol’ come into bearing
very early, usually in the second year after planting and the trees are very productive,
but trees of cv. ‘Alwa’ start to yield later, especially on M.26 rootstock (Czynczyk,
Bielicki, 2002, Uselis, 2002). However, in worse soil conditions, ‘Alwa’ should be
grafted on M.26 rootstock (Kruczyñska, 1998). In this case, planting two-year-old
trees could be a good method of improving the productivity of this cultivar.
Two-year-old trees can be obtained by pruning maiden trees in the spring of
rd
the 3 year of nursery production. According to Bielicki and Czynczyk (1999, 2004)
and Czarnecki (1998), for high quality of planting material, trees should be pruned at
the height of 65 cm.
Pruning at the height of 60 cm improved the feathering of planting material,
without reduction of tree height, in comparison with pruning at the height of 40 cm
(Gudarowska, 2002).
The obtained results showed that for cultivars with strong apical dominance,
‘Ligol’ and ‘Alwa’, the height of pruning should be 100 cm. The pruning at the
height of 100 cm above the soil level positively affected the height of obtained trees
and their feathering. Strong trees pruned in the nursery at the height of 100 cm, had
the most inflorescences in the first years after planting into orchard. However, taking
into consideration the obtained total yield and the tendency of cvs. ‘Alwa’ and ‘Ligol’
to biennial bearing, pruning at the height of 60 cm could be a guarantee of high and
annual yielding.
The differences in the level of yielding between apple trees of cv. ‘Ligol’ and
‘Alwa’ on M.26 rootstock are similar to the results presented by Uselis (2002) in
Lithuania, but the obtained results confirmed the high usefulness of two-year-old
planting material for growing of the estimated cultivar, especially ‘Alwa’.
101
Conclusions. 1. The height of pruning of maiden trees in the spring of
the 3 year of planting material production had a significant influence on the quality
of two-year-old apple trees of cvs. ‘Ligol’ and ‘Alwa’ with one-year-old crown.
2. Irrespective of a cultivar, the best quality of knip-boom type trees was obtained
for trees pruned in a nursery at the height of 100 cm.
3. Pruning at the height of 80 cm improved the height of trees, but pruning at
40 cm and 60 cm positively affected the feathering of planting material of cv. ‘Ligol’.
4. Two-year-old trees of cvs. ‘Ligol’ and ‘Alwa’, pruned at the height of
100 cm and 60 cm were characterized by more intensive blossoming and higher
yield in the first years after planting.
rd
Gauta
2006 05 04
Parengta spausdinti
2006 07 13
References
1. B i e l i c k i P., C z y n c z y k A. Drzewka jabùoni do nowoczesnych sadów
XXI wieku // Zeszyty Naukowe AR Kraków. 1999. No. 351(66). P. 59-65.
2. B i e l i c k i P., C z y n c z y k A. Effect of rootstock quality and height of
heading back one-year-old grafts on the quality of two-year-old trees in nursery // Journal
of Fruit and Ornamental Plant Research. 2004. Vol. 12. P. 61-67.
3. C z a r n e c k i B. Wpùyw wysokoúci przyciæcia drzewek w szkóùce na ich jakoúã
// Zeszyty Naukowe AR w Krakowie. 1998. No. 51(1). P. 411-414.
4. C z y n c z y k A., B i e l i c k i P. Moýliwoúci produkcji drzewek jabùoni o
zróýnicowanej jakoúci // Ogrodnictwo. 2000. 3. P. 12-15.
5. C z y n c z y k A., B i e l i c k i P. Ten-years results of growing the apple
cultivar ‘Ligol’ in Poland // Scientific Works of the Lithuanian Institute of Horticulture and
Lithuanian University of Agriculture. 2002. No. 21(4). P. 12-21.
6. G r e e n G. M. The advantage of feathered trees for more rapid cropping in
apples // Pennsylvania Fruit News. 1991. No 71(4). P. 25-28.
7. G u d a r o w s k a E. Wpùyw wysokoúci przyciêcia jednorocznych okulantów
piæciu odmian jabùoni na jakoúã otrzymanych drzewek dwuletnich // Zeszyty Naukowe
Instytutu Sadownictwa i Kwiaciarstwa. Skierniewice. 2002. Tom 10. P. 75-82.
8. G u d a r o w s k a E., S z e w c z u k A. Wpùyw wysokoúci przyciæcia
okulantów w szkóùce na kwitnienie i owocowanie trzech odmian jabùoni w sadzie // Zeszyty
Naukowe Instytutu Sadownictwa i Kwiaciarstwa. Skierniewice. 2004. Tom 12. P. 43-49.
9. K r u c z y ñ s k a D. Nowe odmiany jabùoni. Hortpress. Warszawa. 1998.
10. U s e l i s N. Assessment of productivity and fruit quality of apple cultivars on
rootstock M26 in fruit bearing orchard // Scientific Works of the Lithuanian Institute of
Horticulture and Lithuanian University of Agriculture. 2002. No. 21(3). P. 14-28.
11. W e r t h e i m S. J. Induction of side-shoot formation in the fruit-tree nursery
// Acta Horticulturae. 1978. No. 80. P. 49-54.
12. V a n O o s t e n H. J. Effect of initial tree quality on field // Acta Horticulturae.
1978. No. 65. P. 123-125.
102
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3). 98–103.
OBELØ GENËJIMO AUKÐÈIO MEDELYNE ÁTAKA JØ KOKYBEI IR
DERLIUI
E. Gudarowska, A. Szewczuk, D. Dereñ
Santrauka
Bandymas atliktas 2001 metais medelyne ir tæstas 2002–2005 metais sode. Treèiaisiais
auginimo medelyne metais ‘Ligol’ ir ‘Alwa’ veisliø sodinukai su M.26 poskiepiu buvo
patrumpinti 40, 60, 80 ir 100 cm aukðtyje nuo dirvos pavirðiaus. 2001 metø rudená buvo
ávertinta dvejø metø sodinukø kokybë.
Aukðèiausi ir didþiausio kamieno skersmens abiejø veisliø vaismedþiai iðaugo
patrumpinus 100 cm aukðtyje. ‘Ligol’ veislës sodinukø trumpinimas 40 ir 100 cm aukðtyje
stimuliavo ðakojimàsi, o ‘Alwa’ veislës obelys daugiau ûgliø iðleido patrumpinus tik
100 cm aukðtyje.
2002 metø pavasará obelys buvo pasodintos sode 3,5 x 1,0 m atstumais.
2002–2004 metais buvo ávertintas kiekvienos obels þiedynø skaièius, 2003–2005 metais –
derlius.
Daugiausia þiedynø pasodinimo metais sukrovë obelys, kurios medelyne buvo
patrumpintos 100 cm aukðtyje. Sode ‘Ligol’ veislës obelys 2003–2005 metais buvo
derlingesnës (22 kg/medis) uþ ‘Alwa’ veislës obelis. 60 ir 100 cm aukðtyje medelyne
patrumpintos ‘Ligol’ ir ‘Alwa’ veislës obelys iðaugino didesná derliø (12,9–24,7 kg/medis)
nei patrumpintos 40 ir 80 cm aukðtyje (11,6–19,7 kg/medis).
Reikðminiai þodþiai: obelys, genëjimo aukðtis, þiedynai, sodinukø kokybë, derlius.
103
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 104–112.
THE EFFECT OF SELECTED AGRICULTURAL
PRACTICES ON QUALITY FEATURES OF APPLE TREES
Jan KOPYTOWSKI, Bogumiù MARKUSZEWSKI,
Jakub GURSZTYN
Uniwersytet Warmiñsko – Mazurski w Olsztynie, Katedra Ogrodnictwa ul.
Prawocheñskiego 21, 10-718 Olsztyn. E-mail: [email protected]
The paper presents the results of studies on production of branched apple trees.
The study was carried out at the nursery owned by Wojciech Gursztyn in Braniewo in
2002–2004. The studies took into consideration not only the applied agricultural technology
operations but also the influence of the specific climatic conditions of the area. Processing
the results an attempt was made to formulate synthesis of the knowledge of the recent
years concerning production of branched trees.
During the study and analysis it was assessed, which of the seven applied agricultural
technique procedures had the largest influence on development of side branches of four
selected, reluctantly branching cultivars of apple trees. The following variants were studied:
I. Controls, II. Pruning, III. Pruning + Arbolin 036 SL (15ml/1 litre of water), IV. Arbolin
036 SL (15ml/1 litre of water), V. Arbolin 036 SL (30ml/1 litre of water), VI. Arbolin 036 SL
(15ml/1 litre of water applied twice), VII. Pruning + Arbolin Extra 038 SL (12ml/1 litre of
water). The trees were trained in the knipboom form (two-year-old trees with one-year-old
crown). The following parameters of the trees were assessed: height, thickness, sum of
lengths and thicknesses of side branches and number of branches with flowers.
Trees of the best quality were produced in those variants where the preparation
called Arbolin 036 SL at 15 ml/1 liter of water was applied. Cultivars: ‘Gloster’, ‘Gala Must’,
‘Elise’ and ‘Ligol’ used for tree study reacted in different ways to operations applied.
Among the analyzed cultivars ‘Gala Must’ reacted the best to Arbolin.
Key words: nurseries, agricultural practices, quality of trees.
Introduction. Nursery trees produced in Poland have to conform to the quality
standards, which oblige producers to grade fruit bearing trees in a consistent manner
(Bielicki, Czynczyk, 2000). Current requirements concerning the nursery tree quality
have been affected by the changes in the technology of tree growing, especially of
apple trees. Views have changed on the bud grafting height, as well as on the issue of
crown formation and the age of planted trees (Úlaski J., 1964; Czynczyk A., 1998;
Mika, 1998; Marczyñski S., 1999; Sadowski and Górski, 2005). Poland’s accession
to the European Union presents additional challenge not only to nursery gardeners
(Makosz, 2004) due to increased requirements concerning the quality of nursery
104
trees and the necessity to adapt to new market conditions. At the same time the
customs and sanitary regulations as well as those concerning the marketing of nursery
trees were made stricter.
This study is an attempt to synthesize the knowledge of the past few years on
the production process of branched apple trees in a nursery and an attempt to answer
the question: which of the seven applied agricultural practices most influences the
producing of offshoots in the four apple tree cultivars.
Materials and methods. The experiment was conducted in a private fruit tree
nursery, situated in the northeast of Poland (Braniewo), near the Vistula Lagoon. The
site where the nursery is situated is on class 4a brown soil with sandy clay layer at
the depth of 40–50 cm. These are well-cultured soils, with regulated air-water relations.
The nurseries were fertilised with ammonium sulphate at 100 kg·ha-1. The fertiliser
was sown approximately on April 20 and at the end of May. Winter wheat and
mustard were used as fore-crops. The nurseries were additionally fertilised through
foliage eight times with Agrolife and Uniwersom up to 1.5 kg·ha-1.
Rootstocks RN-29 (M.9 clone) and M.26 were planted in the spring of 2002, at
a spacing 70 x 10 cm. Cultivar ‘Elisa’ was bud grafted on rootstock M.26, while
cultivars ‘Gloster’, ‘Gala Must’ and ‘Ligol’ were bud grafted on RN-29.
In autumn, soon after the vegetation period had ended, the trees were cut off,
dug out and stored in a refrigerating room for the winter. Early next winter the budgrafted rootstocks were planted in the appropriate places at a spacing 70 x 30 cm,
where the production process proceeded. The plugs were cut out immediately after
planting. A weaker rootstock was used on purpose because it inhibited the growth of
grafted trees and produced single unbranched annual offshoots. The material could
be used to produce biennial trees with one-year-old crown.
The study examined the effect of seven different agricultural practices on the
growth and producing lateral shoots in the four cultivars of apple tree: ‘Elisa’, bud
grafted on rootstock M.26 and ‘Gloster’, ‘Gala Must’ and ‘Ligol’ – on rootstock
RN-29. In early spring of the third year, the grafted trees were cut off 60 cm above
the ground and an annual branched offshoot was formed at the cut-off site, producing
an annual crown on a biennial trunk. At a later stage of the production process, all
offshoots below the place where new crown was formed were removed. The trees
were staked with bamboo poles and fastened with plastic foil to ensure their steady
growth and to protect them from breaking. A number of measures were taken in
order to force the trees to produce offshoots. They were topped and sprayed with
chemical agents in the following combinations: I. Control, II. Topping, III.
Topping + Arbolin 036 SL (15 ml·litre-1 of water), IV. Arbolin 036 SL (15 ml·litre-1 of
water), V. only Arbolin 036 SL (30 ml·litre-1 of water), VI. Arbolin 036 SL
15 ml·litre -1 x 2 (two spraying dates), VII. Topping + Arbolin Extra 038 SL
(12 ml·litre-1 of water). The practices were performed in the first, second and third
decade of June and in the first decade of July. The trees were topped seven times on
5, 9, 15, 21 and 26 of June and on 1 and 6 of July.
The trees were sprayed with Arbolin 036 SL on: 11 of June – 15 ml·litre-1 of
water (objects III, IV and VI), 23 of June – 15 ml·litre-1 of water (object VI), 23 of
June – 30 ml·litre-1 of water (object V) and 23 of June – 12 ml·litre-1 of water
(object VII).
105
In the autumn of 2004, after the vegetation period had ended, the measurements
of tree height, their trunks diameter and offshoot length were taken. The trunk
diameters were measured 30 cm above the ground level.
The statistical analysis was conducted by the method of analysis of variance.
The significance of differences between the mean values was assessed according to
Duncan’s test at the significance level of 0.05. All agricultural and plant protection
practices were performed as recommended.
Results. The fastest growth of trees and the largest number of produced shoots
are observed in June and July at the average air temperature of 21°C. In 2004, the
average temperature in June reached only 14.7°C, and in July – 16.4°C. The average
temperatures of the other months of the vegetation period were not too favourable
either. Due to frequent rains, the vegetation conditions were not good as they brought
about an increase of fungal infections.
The effect of cultivar and agricultural practices on the height of trees is shown
in Table 1. The height of the trees under study was not significantly differentiated
and was affected by the cultivar factor. On average, the trees of cultivar ‘Gala Must’
were the tallest – 163 cm, followed by ‘Gloster’ – 162 cm and ‘Elise’ – 160 cm. The
lowest were the trees of cultivar ‘Ligol’ – average height – 142 cm. The strongest
influence was observed when Arbolin 036 SL was applied at the dose of
30 ml·litre-1 of water, and the weakest – when the trees were topped and Arbolin
Extra 038 SL was applied at the dose of 12 ml·litre-1 of water.
T a b l e 1. The height of trees in the nursery, cm
1
l e n t e l ë. Vaismedþiø aukðtis medelyne, cm
Part I
I dalis
‘Gloster’
‘Gala Must’
‘Elise’
‘Ligol’
160.1 bc
161.0 abc
157.1 c
164.3 ab
167.5 a
164.3 ab
159.5 bc
6.2
162.0 ab
167.8 a
160.1 b
161.7 ab
163.4 ab
169.1 a
163.6 ab
152.3 c
6.8
162.6 a
163.1 ab
154.3 cd
158.0 bc
164.9 a
162.6 ab
167.6 a
50.6 d
5.6
160.2 b
140.2 b
152.3 ab
134.3 c
143.2 ab
148.0 a
143.4 ab
144.5 ab
5.2
142.2 c
Part II
II dalis
I
II
III
IV
V
VI
VII
LSD05/R05
Average of cultivar
Average of
combination
Derinio
vidurkis
157.8 b
154.4 c
152.8 c
158.9 ab
161.8 a
158.7 ab
151.7 c
Veislës vidurkis
LSD05/R05 Part I/ I daliai
Part II / II daliai
Part I x II / I x II daliai
2.2
2.9
5.9
The average values with the same letter are not significantly different at the level of
significance of α = 0.05 / Ta paèia raide paþymëti reikðmiø vidurkiai ið esmës nesiskiria (α = 0,05).
The effect of cultivar and agricultural practices on the intensity of tree growth is
shown in Table 2. The growth intensity did not prove to be significantly differentiated
106
and was also strongly affected by cultivar. The highest mean growth intensity was
observed for cultivar ‘Elise’ – 1.95 cm, whereas the lowest intensity was measured
for ‘Gala Must’ – 1.74 cm. The highest mean growth intensity was obtained with
Arbolin 036 SL at the dose of 15 ml·litre-1 of water, when the agent was applied twice;
the lowest mean growth intensity was recorded in variant II (topping) – 1.79 cm.
T a b l e 2. Intensity of tree growth in the nursery (cm)
2
l e n t e l ë. Vaismedþio augimo medelyne intensyvumas, cm
Part I
I dalis
Part II
‘Gloster’
‘Gala Must’
‘Elise’
‘Ligol’
1.88 a
1.69 a
1.73 a
1.80 a
1.81 a
1.82 a
1.83 a
r. n.
1.79 b
1.61 a
1.72 a
1.85 a
1.70 a
1.83 a
1.65 a
1.79 a
r. n.
1.74 b
1.88 a
1.98 a
1.94 a
1.87 a
1.88 a
1.82 a
1.81 a
r. n.
1.95 a
1.91 a
1.79 a
1.92 a
1.97 a
2.02 a
1.98 a
1.93 a
r. n.
1.93 a
II dalis
I
II
III
IV
V
VI
VII
LSD05/R05
Average of cultivar
Average of
combination
Derinio
vidurkis
1.82 a
1.79 a
1.86 a
1.83 a
1.88 a
1.93 a
1.84 a
Veislës vidurkis
LSD05/R05 Part I/ I daliai
Part II / II daliai
Part I x II / I x II daliai
0.12
n.s.
n.s.
The average values with the same letter are not significantly different at the level of
significance of α = 0.05 / Ta paèia raide paþymëti reikðmiø vidurkiai ið esmës nesiskiria (α = 0,05).
The sum of offshoot length ≥ 20 cm (Table 3) was significantly differentiated
when the applied agricultural practices were the most strongly affecting factor. The
highest mean sum of offshoots length was achieved by cultivar ‘Elise’ and amounted
to 102 cm. The lowest such value was observed for cultivar ‘Gloster’ – 58 cm. The
highest value for the combinations was achieved by the trees in combination III
(Topping + Arbolin 15 ml·litre-1 of water) – 138 cm, while the lowest value was
measured for the control combination (43 cm).
The sum of offshoot length < 20 cm (Table 4) was significantly differentiated
with the combination being the most strongly affecting factor. The highest mean
sum of offshoot length was achieved by cultivar ‘Gala Must’ and amounted to
33 cm. The lowest such value was observed for cultivar Elise – 15 cm. The highest
value for the combinations was achieved by the trees in combination III (Topping +
Arbolin 036 SL 15 ml·litre-1 water) – 32 cm, while the lowest value was measured in
combination I (Control) – 13 cm.
107
T a b l e 3. Sum of tree offshoot over 20 cm length
3
l e n t e l ë. Ilgesniø kaip 20 cm vaismedþio atþalø ilgio suma
Part I
I dalis
Part II
‘Gloster’
‘Gala Must’
‘Elise’
‘Ligol’
31.7 cd
73.8 abc
104.9 a
46.8 bcd
33.2 cd
83.3 ab
29.1 d
39.6
57.5 c
64.8 b
65.8 b
140.8 a
77.3 b
72.2 b
87.1 b
51.8 b
43.4
80.0 b
47.3 d
106.5 bc
177.8 a
66.8 cd
61.5 cd
154.4 ab
96.5 cd
49.4
101.5 a
28.8 c
74.8 bc
116.6 ab
69.0 bc
36.7 c
107.1 ab
147.3 a
48.5
82.9 b
II dalis
I
II
III
IV
V
VI
VII
LSD05/R05
Average of cultivar
Average of
combination
Derinio
vidurkis
43.1 d
80.2 c
138.0 a
65.0 cd
50.9 d
108.0 b
81.2 c
Veislës vidurkis
LSD05/R05 Part I/ I daliai
Part II / II daliai
Part I x II / I x II daliai
16.9
22.3
44.7
The average values with the same letter are not significantly different at the level of
significance of α = 0.05 / Ta paèia raide paþymëti reikðmiø vidurkiai ið esmës nesiskiria (α = 0,05).
T a b l e 4. Sum of tree offshoot under 20 cm length
4
l e n t e l ë. Trumpesniø kaip 20 cm vaismedþio atþalø ilgio suma
Part I
I dalis
Part II
‘Gloster’
‘Gala Must’
‘Elise’
‘Ligol’
Derinio vidurkis
II dalis
I
II
III
IV
V
VI
VII
LSD05/R05
Average of cultivar
Average of
combination
9.6 b
22.2 ab
38.0 a
18.3 b
17.8 b
38.9 a
38.4 a
16.5
26.2 b
22.3 a
22.0 a
40.3 a
34.3 a
35.9 a
35.4 a
39.1 a
n.s.
32.8 a
8.0 c
22.0 ab
25.4 a
12.6 bc
9.3 c
14.9 bc
12.3 bc
9.9
14.9 c
10.7 a
16.8 a
25.2 a
22.3 a
22.9 a
30.6 a
22.5 a
n.s.
21.6 b
12.6 c
20.7 b
32.3 a
21.9 b
21.5 b
30.0 a
28.1 ab
Veislës vidurkis
LSD05/R05 Part I/ I daliai
Part II / II daliai
Part I x II / I x II daliai
5.6
7.4
n.s.
The average values with the same letter are not significantly different at the level of
significance of α = 0.05 / Ta paèia raide paþymëti reikðmiø vidurkiai ið esmës nesiskiria (α = 0,05).
The total number of offshoots ≥ 20 cm (Table 5) was significantly differentiated
with combination being the strongest affecting factor. The largest average total number
of offshoots was achieved by the trees of cultivar ‘Elise’ – 2.9. The lowest such
number was observed for the cultivar ‘Gloster’ – 1.8 per tree. The highest total
number of offshoots for combinations was observed for the trees of combination
108
III (Topping + Arbolin 036 SL 15 ml·litre-1 of water) – 3.9, while the lowest average
total number of offshoots was recorded for the control combination – 1.3.
T a b l e 5. The number of offshoots equal to 20 cm
5
l e n t e l ë. 20 cm ilgio vaismedþio atþalø ilgio suma
Part I
I dalis
Part II
‘Gloster’
‘Gala Must’
‘Elise’
‘Ligol’
1.0 c
2.0 abc
2.9 a
1.6 bc
1.3 c
2.8 ab
1.1 c
1.2
1.8 b
2.1 b
21. b
4.1 a
2.3 b
2.0 b
2.7 b
1.7 b
1.3
2.4 a
1.5 d
3.1 bc
4.8 a
2.0 cd
1.9 cd
4.3 ab
2.7 cd
1.4
2.9 a
0.7 c
2.1 bc
3.7 a
2.1 bc
1.0 c
3.3 ab
4.2 a
1.4
2.4 a
II dalis
I
II
III
IV
V
VI
VII
LSD05/R05
Average of cultivar
Veislës vidurkis
LSD05/R05 Part I/ I daliai
Part II / II daliai
Part I x II / I x II daliai
Average of
combination
Derinio
vidurkis
1.3 c
2.3 b
3.9 a
2.0 bc
1.5 c
3.3 a
2.4 b
0.5
0.7
1.3
The average values with the same letter are not significantly different at the level of
significance of α = 0.05 / Ta paèia raide paþymëti reikðmiø vidurkiai ið esmës nesiskiria (α = 0,05).
The effect of apple tree cultivar and agricultural practices on the total number
of offshoots < 20 cm is shown in Table 6.
T a b l e 6. The number of offshoots over 20 cm
6
l e n t e l ë. Ilgesniø kaip 20 cm vaismedþio atþalø skaièius
Part I
I dalis
Part II
‘Gloster’
‘Gala Must’
‘Elise’
‘Ligol’
Derinio vidurkis
II dalis
I
II
III
IV
V
VI
VII
LSD05/R05
Average of cultivar
Average of
combination
1.2 c
2.6 bc
3.9 ab
2.2 bc
2.4 bc
4.5 a
4.1 ab
1.7
3.0 b
3.6 a
2.8 a
4.3 a
4.3 a
4.5 a
4.7 a
5.3 a
r.n.
4.2 a
1.0 b
2.8 a
3.2 a
1.7 b
0.9 b
1.7 b
1.5 b
1.1
1.8 d
1.3 a
1.5 a
2.6 a
2.7 a
2.8 a
3.2 a
2.7 a
r.n.
2.4 c
1.8 d
2.4 cd
3.5 a
2.7 abc
2.7 abc
3.5 a
3.4 ab
Veislës vidurkis
LSD05/R05 Part I/ I daliai
Part II / II daliai
Part I x II / I x II daliai
0.6
0.7
1.5
The average values with the same letter are not significantly different at the level of
significance of α = 0.05 / Ta paèia raide paþymëti reikðmiø vidurkiai ið esmës nesiskiria (α = 0,05).
109
The total number of offshoots < 20 cm was significantly differentiated with
combination being the strongest affecting factor. The largest average total number
of offshoots was achieved by the trees of ‘Gala Must’ – 4.2. The lowest such
number was observed for cultivar ‘Elise’ – 1.8. The highest average total number of
offshoots for combinations was observed for the trees of combination III (Topping
+ Arbolin 036 SL 15 ml·litre-1 of water) and VI (Arbolin 036 SL 15 ml·litre-1 of water
x 2); in both cases the number was 3.5, while the lowest average total number of
offshoots was recorded for the control combination – 1.8.
Discussion. Weather conditions in the third year of running the nursery were
not favourable for producing young trees. Differentiation in growth among the breeding
cultivars, associated with genotype, rootstock, apical dominance, weather conditions
and performed agricultural practices has been observed. This was the most evident
in cultivar ‘Elise’. According to Jaumieñ (2004), the used rootstock does not play
any important role in branching grafted trees of cultivar ‘Elise’. They produce a
similar number of long and short offshoots on dwarf (M.9 and PB 4) and semidwarf (M.26) rootstocks. Considering the above, it must be said that good growth
and offshoot development was also observed for cultivar ‘Elise’ in Braniewo. The
number of long offshoots was similar to the number of the short ones.
Cultivar ‘Gloster’ is one of those, which do not branch easily (Basak, 2001).
The proposition can be substantiated in the light of the results of this study, as the
sum of offshoot length ≥ 20 cm for the cultivar was the smallest, as was the total
number of offshoots; similar results were obtained by Kopytowski (2002).
The research conducted by Jaumieñ and Dziuban (1998) indicates that the Gala
cultivar treated with Arbolin produced the largest number of side shoots. In the
study conducted near Braniewo, the trees of the same cultivar grown in a three year
cycle branched well, producing 2.4 offshoots ≥ 20 cm and 4.2 ones < 20 cm.
Winter apple cultivar ‘Ligol’ is well known to fruit farmers, which also makes it
popular among nursery gardeners. The best quality of the trees in a three year cycle
is obtained, regardless of other measures, by cutting one-year-old trees 60 cm above
the ground (Rejman et al., 2002; Gudarowska, Szewczyk, 2004). In the study, the
cultivar was effective in producing offshoots, both long and short ones.
Conclusions. 1. The tallest grown trees were those of cultivar ‘Gala Must’ –
162.6 cm; the lowest were those of cultivar ‘Ligol’ – 142 cm. The tallest trees were
obtained in combinations where Arbolin 036 SL was applied at the dose of 30 ml·l-1
of water; the lowest trees grew in the group, which were topped manually and
treated with Arbolin Extra 038 SL at the dose of 12 ml·l-1 of water.
2 The largest trunk diameter increase was observed in trees of cultivar ‘Elise’
(1.95 cm), the smallest – of cultivar ‘Gala Must’. The differentiation was not affected
by the practices applied, but only by cultivar features.
3. The highest sum of offshoots growth over 20 cm was observed of cultivar
‘Elise’ in the variant where Arbolin 036 SL was applied at the dose of 15 ml·l-1 of
water.
Gauta
2006 05 30
Parengta spausdinti
2006 07 17
110
References
1. B a s a k A. O rozgaùæzianiu drzewek w szkóùkach owocowych. OWK. 2001. 12 p.
2. B i e l i c k i P., C z y n c z y k A. Wpùyw wysokoúci ciæcia drzewek
jednorocznych w szkóùce na jakoúã drzewek dwuletnich. XLIII Ogólnopolska Naukowa
Konferencja Sadownicza. Doskonalenie metod produkcji owoców zgodnie z wymogami
UE. ISiK Skierniewice, 2004. P. 57–58.
3. C z y n c z y k A. Podkùadki sùabo rosnàce podstawowym czynnikiem
intensyfikacji sadów. XXXVII Ogólnopolska Naukowa Konferencja Sadownicza. ISiK
Skierniewice, 1998. P. 101–110.
4. G u d a r o w s k a E., S z e w c z y k A. Wpùyw wysokoúci przyciæcia
okulantów w szkóùce na kwitnienie drzew w sadzie. XLIII Ogólnopolska Naukowa
Konferencja Sadownicza. Doskonalenie metod produkcji owoców zgodnie z wymogami
UE. ISiK Skierniewice, 200ùywa na rozgaùæzianie drzewek jabùoni w szkóùce? Szkóùkarstwo,
2004. 4 p.
5. J a u m i e ñ F., D z i u b a n R. Wpùyw Arbolinu 036 SL i maúci Aarbolin PA
na rozgaùæzianie okulantów jabùoni w latach 1995 i 1997. XXXVII Ogólnopolska Naukowa
Konferencja Sadownicza. ISiK Skierniewice, 1998. P. 25–30.
6. K o p y t o w s k i J. Doskonalenie metod produkcji sadowniczego materiaùu
szkóùkarskiego. Wyd. UWM Olsztyn, 2002.
7. M a k o s z E. Przyszùoúã szkóùkarstwa sadowniczego. Szkóùkarstwo, 2004. 1 p.
8. M a r c z y ñ s k i S. Szkóùkarstwo Polskie 1779-1999. Agencja ZYX- Poligrafia.
1999.
9. M i k a A. Modele sadów XXI wieku. XXXVII Ogólnopolska Naukowa
Konferencja Sadownicza. ISiK Skierniewice, 1998. P. 75–76.
10. R e j m a n A., Ú c i b i s z K., C z a r n e c k i B. Szkóùkarstwo roúlin
sadowniczych. PWRiL, Warszawa, 2002. P. 239–240.
11. S a d o w s k i A., G ó r s k i M. Jakie drzewka dwuletnie? Szkóùkarstwo,
2005. 1 p.
12. Ú l a s k i J. Szkóùkarstwo sadownicze. PWRiL Warszawa, 1964.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
104–112.
KAI KURIØ TECHNOLOGINIØ PRIEMONIØ ÁTAKA OBELØ KOKYBËS
RODIKLIAMS
J. Kopytowski, B. Markuszewski, J. Gursztyn
Santrauka
Tyrimai atlikti 2002–2004 m. Wojciecho Gursztyno privaèiame medelyne Braniewo
gyvenvietëje. Buvo atsiþvelgta ne tik á taikytas technologijas, bet ir á specifiniø to regiono
klimato sàlygø átakà. Apdorojant rezultatus, buvo pamëginta susisteminti pastaraisiais
metais sukauptà informacijà apie ðakotø vaismedþiø auginimà.
Tyrinëjant ir analizuojant buvo ávertinta, kuri ið septyniø panaudotø technologiniø
priemoniø labiausiai paveikë keturiø pasirinktø sunkiai besiðakojanèiø obelø veisliø ðoniniø
ðakø vystymàsi. Bandymo variantai buvo tokie: I. Kontrolë, II. Pinciravimas,
111
III. Pinciravimas + Arbolin 036 SL (15 ml/1 vandens), IV. Arbolin 036 SL (15 ml/1 vandens),
V. Arbolin 036 SL (30 ml/1 vandens), VI. Arbolin 036 SL (15 ml/1 vandens – du kartus),
VII. Pinciravimas + Arbolin Extra 038 SL (12 ml/1 vandens). Vaismedþiai buvo suformuoti
„knipo“ formos (dvejø metø vaismedþiai su vieneriø metø vainiku). Ávertinti ðie vaismedþiø
rodikliai: aukðtis, storis, ðoniniø ðakø ilgio ir storio suma, þydinèiø ðakø skaièius.
Geriausios kokybës vaismedþiai iðaugo panaudojus Arbolin 036 SL preparatà
(15 ml/1 vandens). Tirtos veislës: ‘Gloster’, ‘Gala Must’, ‘Elise’ ir ‘Ligol’, á skirtingus
apdorojimus reagavo skirtingai. Ið visø tirtø veisliø á Arbolin geriausiai reagavo ‘Gala
Must’.
Reikðminiai þodþiai: medelynai, agrotechninës priemonës, vaismedþiø kokybë.
112
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 113–123.
PERFORMANCE OF DWARFING CHERRY ROOTSTOCKS
IN THE NORTHEASTERN UNITED STATES
Terence L. ROBINSON1, Stephen A. HOYING2,
Robert L. ANDERSEN1
1
Department of Hort. Sciences, New York State Agricultural Experiment
Station, Cornell University, Geneva, NY 14456, USA.
E-mails: [email protected], [email protected]
Cornell Cooperative Extension, 1581 Rt. 88 N, Newark, NY 14568 USA.
E-mail: sah192cornell.edu
2
Sweet cherry rootstocks and training systems were compared in two field planting
(1999 and 2002). In the 1999 trial, ‘Hedelfinger’ was planted with three rootstocks (Gisela
5, (Gi.5), Gisela 6, (Gi.6) and MxM.2), while ‘Lapins’ and ‘Sweetheart’ were planted on Gi.5
and Gi.6. After 7 years, tree size was smallest with Gi.5, intermediate with Gi.6 and largest
with MXM.2. Early yield and cumulative yield were highest for trees on Gi.5 followed by
Gi.6, while trees on MXM.2 had the lowest yield. Average fruit size was largest on Gi.6,
intermediate on MXM.2 and smallest on Gi.5. Among planting systems, the vertical axis
system had the highest cumulative yield/ha followed by the slender spindle system, the
V system, the Marchant system, the Spanish bush system and the central leader system.
The cumulative yields largely reflected density; however, the Marchant system had
significantly lower yield than expected from its density, while the vertical axis system had
higher yield than expected from its density. In the 2002 field trial, ‘Lapins’, ‘Regina’ and
‘Hudson’ were planted on Mazzard, Gi.12, Gi.5 and Gi.6. After 4 years the Gi.12 trees were
as large as the trees on Mazzard, while Gi.6 was intermediate and Gi.5 was significantly
smaller. Gi.5 had the highest yield followed by Gi.6, and Gi.12, while Mazzard had
substantially lower yield than any of the Gisela rootstocks. The combination of Gi.5
rootstock and vertical axis training with ‘Regina’ achieved a yield of 12 t/ha of large
cherries in the fourth year.
Key words: Prunus avium, Gisela rootstocks, yield, fruit size, training system, planting
density.
Introduction. New cherry varieties that are large, firm and resist rain-induced
cracking have created new opportunities for the production of sweet cherries in the
eastern USA (Kappel, 2002). In addition the use of rain exclusion shelters or automatic
calcium sprinkling systems can be used to limit rain induced cracking. Nevertheless,
traditional, vigorous, non-precocious rootstocks continue to limit early yield and
113
cause tree containment problems as new orchards mature. The development of
precocious, dwarfing rootstocks has allowed the development of high-density cherry
orchards with smaller trees that have the potential to significantly improve grower
returns (Lang, 2000; Long, 2001; Perry et al., 1996; Robinson, 2005). Several highdensity training systems have been developed for sweet cherries (Balmer, 2001;
Long, 2001; Perry, 1998; Zahn, 1994) giving fruit growers many options for choosing
a planting density, rootstock and training protocol. The objective of this project was
to compare both standard and dwarfing rootstocks trained to several high-density
production systems for sweet cherries.
Materials and Methods. In April of 1999 a replicated field trial was planted at
Geneva, New York State, USA with ‘Hedelfinger’ on three rootstocks (Gi.5, Gi.6
and MxM.2), ‘Lapins’ and ‘Sweetheart’ on 2 rootstocks (Gi.5 and Gi.6) and
‘Tehranivee’ and ‘Regina’ on one rootstock (Mahaleb). Each variety/rootstock
combination was planted into each of six training systems: (central leader
(336 trees/ha), Spanish bush (673 trees/ha), slender spindle (897 trees/ha), V-system
(997 trees/ha), Marchant inclined tree system (1035 trees/ha) and vertical axis
(1196 trees/ha)). The training recipes for each system were published earlier
(Robinson et al., 2004). The plot was designed as a split plot randomized complete
block experiment with 3 main plot replications. Training system was the main plot
with each main plot consisting of three 32 m long rows. Each row was planted on
a broad 30 cm high berm to control winter damage associated with excessive soil
moisture. In addition, a subsurface soil drainage line was installed in the center of
each tractor alley to remove excess moisture in the spring and during heavy rainfalls
before harvest. Each main plot was divided into 9 variety x rootstock subplots (3 in
each row). Each sub plot had from 2 to 6 trees of each variety x rootstock x system
combination with the number of trees depending on the inrow spacing of the system.
In May of 2002 a second replicated field trial was planted at Geneva, New York
State, USA with ‘Lapins’, ‘Regina’ and ‘Hudson’ on four rootstocks (Gi.5, Gi.6,
Gi.12 and Mazzard seedling). Each variety/rootstock combination was planted into
each of four training systems: (steep leader (598 trees/ha, Spanish bush
(748 trees/ha), slender spindle (748 trees/ha), and vertical axis (997 trees/ha)). The
plot was designed as a split plot randomized complete block experiment with 3 main
plot replications. Training system was the main plot with each main plot consisting
of two 50 m long rows. Each main plot was divided into 8 variety x rootstock
subplots (4 in each row). Each sub plot had from 4 to 7 trees of each variety x
rootstock x system combination with the number of trees depending on the inrow
spacing of the system.
In both plots yield and fruit size data recorded each year. A 50 cherry sample
was collected each year from each tree and analyzed for proportion of cracked fruit
and fruit soluble solids. Economic crop value was calculated as: Crop Value ($/ha)
= (Cumulative yield (kg/ha) – yield of cracked fruit (kg/ha)) * $2.20/kg. Data were
analyzed by analysis of variance. Effect of rootstock in the 1999 plot was determined
only with ‘Hedelfinger’ while the effect of system was determined using all 6 varieties.
In the 2002 plot the effect of rootstock and system was determined using both
‘Lapins’ and ‘Regina’.
114
Results. T r e e s u r v i v a l a n d t r e e s i z e. Tree losses in both
plots were greatest on Mazzard followed by Mahaleb and MXM.2 and Gi.12 (Table).
There were essential not tree losses with Gi.5 or Gi.6 in either plot. Tree death was
due to root rot and winter injury. There was a clear rootstock effect on tree size, as
measured by trunk cross-sectional area, with trees on Gi.5 being significantly smaller
(21%) than trees on Gi.6, which in turn were about 9% smaller than trees on MXM.2
(Figure 1A). Planting system also had a significant effect on final trunk cross-sectional
area. The central leader trees were the largest and the Marchant trellis trees were the
smallest. There was a significant negative curvilinear relationship between tree planting
density and tree size with the highest density vertical axis trees being only 60% as
large as the lowest density central leader trees (Figure 1B).
T a b l e. Tree death in 2 large orchard systems trials at Geneva NY, USA
L e n t e l ë.
Vaismedþiø þuvimas dviejuose dideliuose sodø sistemø bandymuose
Þenevoje, Niujorko valstijoje, JAV
Plot / Sklypas
1997 Plot / Sklypas 1997 m.
2002 Plot / Sklypas 2002 m.
Rootstock / Poskiepis
Mahaleb
MXM.2
Mazzard
Gi.12
Gi.6
Gi.5
8%
---
4%
---
--16%
--4%
0.1%
1.6%
0.1%
1.4%
F i g. 1. (A) Effect of rootstock on final tree size (trunk cross-sectional area (cm2))
after 7 years of ‘Hedelfinger’ sweet cherry. Vertical bars represent LSD for
≤0.05. (B) Relationship of tree density and
significant differences between stocks, p≤
final tree size (TCSA) after 7 years of 5 sweet cherry varieties (‘Hedelfinger’,
‘Lapins’, ‘Sweetheart’, ‘Regina’ and ‘Tehranivee’) on MXM.2, Gisela 5, Gisela 6 and
≤0.05.
Mahaleb rootstocks trained to 6 training systems. Regression significant, p≤
1 p a v. (A) Poskiepio átaka galutiniam vaismedþio dydþiui (kamieno skerspjûvio
plotui, cm 2) po 7 ‘Hedelfinger’ veislës treðniø augimo metø. Vertikalûs stulpeliai
≤ 0,05. (B) Galutinio vaismedþio dydþio
vaizduoja esminius skirtumus tarp poskiepiø, p≤
(KSP) priklausomumas nuo vaismedþiø tankumo po 7 metø. Tirtos penkios treðniø
veislës (‘Hedelfinger’, ‘Lapins’, ‘Sweetheart’, ‘Regina’ ir ‘Tehranivee’) su MXM.2, Gisela
5, Gisela 6 ir Mahaleb poskiepiais. Vaismedþiai formuoti pagal 6 formavimo sistemas.
≤ 0,05.
Lygtis patikima, kai p≤
115
Y i e l d. With ‘Hedelfinger’, Gi.5 had the greatest cumulative yield
(30 kg/tree), while Gi.6 was intermediate (18 kg/tree) and MXM.2 had the lowest
yield (7 kg/tree) (Figure 2A). In the winter preceding 2004 severe winter temperatures
killed most of the flower buds in this trial. The drop in yield from 2003 to 2004
shows that Gi.6 was the most sensitive to winter cold while MXM2 was the least
sensitive. Gi.5 was intermediate.
F i g. 2. (A) Effect of rootstock on cumulative yield/ha of ‘Hedelfinger’ sweet cherry
trees trained to 6 training systems. Vertical bars represent LSD for significant
≤0.05. (B) Relationship of tree planting density to
differences between stocks, p≤
cumulative yield after 7 years of 5 sweet cherry varieties (‘Hedelfinger’, ‘Lapins’,
‘Sweetheart’, ‘Regina’ and ‘Tehranivee’) on MXM.2, Gisela 5, Gisela 6 and Mahaleb
≤0.05.
rootstocks trained to 6 training systems. Regression significant, p≤
2
p a v. (A) Poskiepio átaka suminiam ‘Hedelfinger’ veislës treðniø, suformuotø pagal
6 formavimo sistemas, derliui ið hektaro. Vertikalûs stulpeliai vaizduoja esminius
≤ 0,05. Suminio derliaus priklausomumas nuo nuo
skirtumus tarp poskiepiø p≤
vaismedþiø tankumo po 7 metø. Tirtos penkios treðniø veislës (‘Hedelfinger’, ‘Lapins’,
‘Sweetheart’, ‘Regina’ and ‘Tehranivee’) su MXM.2, Gisela 5, Gisela 6 ir Mahaleb
poskiepiais. Vaismedþiai formuoti pagal 6 formavimo sistemas. Lygtis patikima, kai
≤ 0,05.
p≤
Among systems averaged over all 5 varieties, the vertical axis system had the
highest yield per tree in the third year (2001) followed by the slender spindle system,
the Spanish bush, central leader, Marchant inclined tree and the V system, respectively
(Figure 3A). By the seventh year, yield ranged from 7-19 kg/tree and from 7-16 t/ha.
The highest cumulative yield/ha was with the vertical axis system (37 t/ha), followed
by the slender spindle system (27 t/ha), the V system (25 t/ha), the Spanish bush
system (19 t/ha), the Marchant inclined tree system (18 t/ha), and the central leader
system (11 t/ha) (Figure 3B).
Among varieties, ‘Sweetheart’ was the most productive followed by
‘Tehranivee’, ‘Lapins’, ‘Hedelfinger’ and lastly ‘Regina’ (data not shown). ‘Regina’
had significantly lower production than any of the other varieties in the 1999 plot but
in the 2002 plot it had the highest production. Following the winter of 2004, which
killed most flower buds on ‘Sweetheart’ and ‘Lapins’ and many flower buds on
‘Hedelfinger’, ‘Regina’ had the highest flower bud survival.
116
F i g. 3. Annual yield/tree (A) and yield/ha (B) of 5 sweet cherry varieties
(‘Hedelfinger’, ‘Lapins’, ‘Sweetheart’, ‘Regina’ and ‘Tehranivee’) on MXM.2, Gisela 5,
Gisela 6 and Mahaleb rootstocks at Geneva NY. Vertical bars represent LSD for
≤0.05.
significant difference within each year, p≤
3 p a v. Penkiø treðniø veisliø (‘Hedelfinger’, ‘Lapins’, ‘Sweetheart’, ‘Regina’ ir
‘Tehranivee’) vaismedþiø su MXM.2, Gisela 5, Gisela 6 ir Mahaleb poskiepiais metinis
derlius ið vaismedþio (A) ir ið hektaro (B), Þeneva, Niujorko valstija. Vertikalûs
≤ 0,05.
stulpeliai vaizduoja esminius skirtumus kiekvienais metais, p≤
The differences in yield between systems were largely a function of tree density.
There was a linear relationship of tree planting density and yield that explained 67%
of the variation in cumulative yield per hectare (Figure 2B). The Marchant system,
and to some extent the V system, had significantly lower cumulative yield than expected
from their tree density. The vertical axis system, and to a lesser extent the slender
spindle system, had a higher cumulative yield than expected from their tree density.
With the vertical axis system, this resulted from the highest yield per tree and the
highest tree density.
There was an interaction of rootstock and training system with ‘Hedelfinger’,
but not with ‘Lapins’ and ‘Sweetheart’. The combination of vertical axis training
and Gi.5 rootstock resulted in very high 7-year cumulative yields per hectare of 46,
41 and 40 t/ha for ‘Hedelfinger’, ‘Lapins’ and ‘Sweetheart’, respectively. In contrast,
the vertical axis system with the full vigor MXM.2 rootstock had a cumulative yield
of only 13 t/ha with ‘Hedelfinger’.
Y i e l d E f f i c i e n c y. There was a large effect of rootstock on yield
efficiency. Trees on Gi.5 were 4 times as efficient as trees on MXM.2 (data not
shown). Trees on Gi.6 were intermediate. Among training systems, the vertical axis
system was substantially more efficient than any other system and almost twice as
efficient as the traditional central leader system. There was a significant positive
curvilinear relationship between tree density and yield efficiency (data not shown).
However, the Marchant trellis and the V-slender spindle were significantly less efficient
than predicted by the regression equation.
F r u i t Q u a l i t y. With ‘Hedelfinger’, the largest average fruit size over
the 5 cropping seasons was with Gi.6, while MXM.2 was intermediate and Gi.5 had
the smallest fruit size (Figure 4A). However, there was an interaction with variety.
117
With ‘Lapins’ and ‘Sweetheart’ there was no difference in fruit size between Gi.5
and Gi.6 (data not shown). Among training systems, average fruit size was greatest
for the central leader, followed by the slender spindle, Marchant Spanish bush,
V-slender spindle, and vertical axis systems, respectively. Although the difference
between the top 2 systems and the bottom 2 systems was significant, the differences
were not large (Figure 4B).
F i g. 4. (A) Effect of rootstock on average fruit size of ‘Hedelfinger’ sweet cherry
trees at Geneva NY. (B) Effect of training system on average fruit size of 5 sweet
cherry varieties (‘Hedelfinger’, ‘Lapins’, ‘Sweetheart’, ‘Regina’ and ‘Tehranivee’), on
MXM.2, Gisela 5, Gisela 6 and Mahaleb rootstocks at Geneva NY. Vertical bars
≤0.05.
represent LSD for significant differences between stocks or systems, p≤
4
p a v. (A) Poskiepio átaka vidutiniam ‘Hedelfinger’ veislës treðniø vaisiø dydþiui,
Þeneva, Niujorko valstijoja. (B) Formavimo sistemos átaka penkiø treðniø veisliø
(‘Hedelfinger’, ‘Lapins’, ‘Sweetheart’, ‘Regina’ ir ‘Tehranivee’) su MXM.2, Gisela 5,
Gisela 6 ir Mahaleb poskiepiais vidutiniam vaisiø dydþiui, Þeneva, Niujorko valstija.
≤ 0,05.
Vertikalûs stulpeliai vaizduoja esminius skirtumus tarp poskiepiø ar sistemø, p≤
E c o n o m i c s. Cumulative crop value was greatest for trees on Gi.5
followed by Gi.6 and then MXM.2 (Figure 5A). Among rootstocks there was an
interaction with variety. With ‘Hedelfinger’ and ‘Lapins’, the largest cumulative crop
value was with Gi.5, intermediate with Gi.6 and smallest with MXM.2. With
‘Sweetheart’, there was no difference in cumulative crop value between Gi.5 and
Gi.6. Among systems, cumulative crop value over the first 6 years of the orchards
life was greatest for the vertical axis system ($68,600/ha), followed by the slender
spindle system ($47,000/ha), the V system ($46,900/ha), the Spanish bush system
($34,200/ha), the Marchant inclined tree system ($30,600/ha), and the central leader
system ($20,000/ha). The difference between the top system and the bottom system
was 3.4 fold. There was a significant positive curvilinear relationship between tree
density and crop value (Figure 5B). The Marchant trellis had significantly lower
cumulative crop value than predicted by the regression relationship.
118
2 0 0 2 T r i a l. Tree size after 4 years was smallest for Gi.5 (Figure 6).
Gi.6 was intermediate, while Gi.12 and Mazzard were the largest and not significantly
different. Cumulative yield over the first 4 years was inversely related to tree vigor.
The highest yield was with Gi.5, followed by Gi.6, Gi.12 and Mazzard. Although Gi.12
was similar in tree size to ‘Mazzard’ it had 2.7 times as much yield as Mazzard. ‘Regina’
was more productive than ‘Lapins’ due to cold damage of ‘Lapins’ flower buds in the
winter of 2004/2005. The combination of Gi.5 rootstock and vertical axis training with
‘Regina’ achieved a yield of 12 t/ha of large cherries in the fourth year.
F i g. 5. (A) Effect of rootstock on 7-year cumulative crop value per hectare of
‘Hedelfinger’ sweet cherry trees at Geneva NY. Vertical bars represent LSD for
≤0.05. (B) Relationship of tree density and
significant difference between rootstocks, p≤
6-year cumulative crop value per hectare of 5 sweet cherry varieties (‘Hedelfinger’,
‘Lapins’, ‘Sweetheart’, ‘Regina’ and ‘Tehranivee’), on MXM.2, Gisela 5, Gisela 6 and
Mahaleb rootstocks trained to 6 planting systems at Geneva NY (B). Regression
≤0.05.
significant, p≤
5
p a v. (A) Poskiepio átaka ‘Hedelfinger’ veislës treðniø 7 metø suminio derliaus ið
hektaro vertei, Þeneva, Niujorko valstija. Vertikalûs stulpeliai vaizduoja esminius
≤ 0,05. (B) Penkiø treðniø veisliø (‘Hedelfinger’, ‘Lapins’,
skirtumus tarp poskiepiø, p≤
‘Sweetheart’, ‘Regina’ ir ‘Tehranivee’) vaismedþiø su MXM.2, Gisela 5, Gisela 6 ir
Mahaleb poskiepiais, suformuotø pagal; 6 formavimo sistemas, 6 metø suminio derliaus
ið hektaro vertës priklausomumas nuo tankumo, Þeneva, Niujorko valstija. Lygtis
≤ 0,05.
patikima, kai p≤
Discussion. Our results show the value of the precocious Gisela rootstocks
for early production (Balmer, 2001; Lang, 2000; Perry et al, 1996). The Gisela 5
trees had 10 times the yield as the vigorous MxM.2 trees in the fourth year, 4 times
the cumulative yield after 7 years. The ‘Gisela 6’ trees had about 7 times the yield of
the MxM.2 trees in the fourth year and 2.5 times the cumulative yield after 7 years.
In addition, the Gisela trees have had better survival in both plots and have remained
smaller than the ‘Mazzard’ or the MxM.2 trees and have a more “calm” appearance,
which makes them more suited to high planting densities. The Gi.6 trees have had
larger fruit size and higher fruit soluble solids than the standard sized MxM.2 trees
indicating that they have not been over-cropped. In contrast, the Gi.5 trees had
such large crops that fruit size and soluble solids were both lower than the Gi.6
119
trees. This indicates that the Gi.5 trees were resources limited for fruit development.
With the larger fruited ‘Regina’ variety Gi.5 produced a very large 4th year crop with
large fruit size. However, with self fruitful varieties such as ‘Sweetheart’ and ‘Lapins’
a modified pruning strategies such as heading of all one-year-old shoots will be
required to achieve marketable fruit size. It is also possible that the large crops on
Gi.5 may be limiting tree carbohydrate or nitrogen reserve accumulation, thus
increasing vulnerability to winter damage (Andersen, et al, 1999; Lang and Ophardt,
2000). Our results after the winter of 2004 indicate that both Gi.6 and Gi.5 may be
more vulnerable to severe winter temperatures than the full vigor MXM.2. Gi.12
appears to be a full vigor rootstock but with greater precocity than Mazzard.
F i g. 6. Final tree size (trunk cross-sectional area (cm2)) after 4 years (A) and fouryear cumulative yield/ha (B) of ‘Regina’ and ‘Lapins’ sweet cherry on Mazzard, Gisela
5, Gisela 6 and Gisela 12 rootstocks at Geneva NY. Vertical bars represent LSD for
≤0.05.
significant differences between stocks, p≤
6 p a v. ‘Regina’ ir ‘Lapins’ veisliø treðniø su Mazzard, Gisela 5, Gisela 6 ir Gisela 12
poskiepiais galutinis vaismedþio dydis (kamieno skerspjûvio plotas, cm 2) po 4 metø (A)
ir ketveriø metø suminis derlius ið hektaro (B), Þeneva, Niujorko valstija. Vertikalûs
≤ 0,05.
stulpeliai vaizduoja esminius skirtumus tarp poskiepiø, p≤
The strong correlation of tree planting density and cherry yield over the first
7 years is similar to the results of studies of planting density with apple (Robinson,
2003). With our cherry data the relationship appears to be exponential over the
densities we considered, whereas with apple, the relationship is asymptotic. It is
likely, that over a broader range, the relationship with cherry would also be asymptotic.
An important component of the high yields of the vertical axis and the slender
spindle systems, was the minimal pruning during the first 2 years. In contrast, the
Spanish Bush system had very severe pruning during the first 2 years. The
perpendicular V system had severe pruning at planting, but minimal pruning after
that. The severe pruning was related to lower yields of these systems in the 3rd and
4th years. To successfully incorporate minimal pruning with sweet cherry, requires
specialized branching techniques to overcome the strong apical dominance. Bud
removal early in the spring has been very successful at stimulating lateral bud
120
development without heading the leader (Hoying et al., 2001). This technique allows
minimal pruning yet proper limb placement along the leader.
The reduction in tree size (as measured by trunk cross-sectional area) with
increasing tree density indicates that at higher tree densities trees can be managed in
the smaller allotted space for a greater period of time. It was of interest to note that
in the vertical axis system with renewal pruning (Zahn, 1994), all of the lateral limbs
on each tree were less than 10cm in diameter. Larger limbs were removed back to
10 cm stubs and replacement branches were developed. In contrast, the central
leader trees had lower scaffold branches that exceeded 25cm in diameter by the end
of the 7th year. The larger branch structure of the central leader trees led to larger
trunks and probably much larger root systems and more tree vigor.
Considering yield, fruit size, soluble solids and gross economic returns, the
vertical axis, slender spindle and the V-system were the three best systems in this
trial. The slender spindle and the V-system combined relatively high yields with good
fruit size and quality. The vertical axis system was highly productive, but had slightly
smaller fruit size and soluble solids content. The large fruit size and the high soluble
solids content with the slender spindle and the V-system indicate that these systems
were not over-cropped, whereas, the smaller fruit size and lower sugar content of
the vertical axis system indicates this system was slightly over-cropped. To make
the vertical axis system perform better will require modified pruning strategies such
as annual heading of one-year-old lateral shoots to reduce the cropping potential of
the system.
‘Regina’ cherry appears to be highly adapted variety to New York State climate.
The tree had good survival and better winter bud hardiness than the other varieties
we tested. Fruit size was large and tolerant of rain cracking. Although yield was low
in our 1999 trial where it was planted on Mahaleb rootstock, or in the 2002 trial
when planted on Mazzard, yield was highest when planted on Gisela stocks in the
2002 plot. An additional reason why yields were high in the second trial was that we
utilized a late blooming variety from New York State, ‘Hudson’ to pollinate ‘Regina’.
Conclusions. Our results show that planting systems, which use much higher
tree densities than the common central leader system combined with new precocious
rootstocks and minimal pruning, can give substantial yields in the first 5 years and
provide significant gross returns. With a high value crop like sweet cherries, this
should help rapidly recoup the investment associated with planting a new cherry
orchard (Seavert, 1997; Weber, 1998).
Gauta
2006 07 25
Parengta spausdinti
2006 08 08
121
References
1. A n d e r s e n, R. L., T. L. R o b i n s o n and G. A. L a n g. 1999.
Managing the Gisela cherry rootstocks. New York Fruit Quarterly 7(4):19–22.
2. B a l m e r, M. 2001. Sweet cherry tree densities and tree training. Compact
Fruit Tree. 34(3):75–77.
3. H o y i n g, S. A., T. L. R o b i n s o n and R. L. A n d e r s e n. 2001.
Improving sweet cherry branching. New York Fruit Quarterly 9(1): 19–22.
4. K a p p e l, F. 2002. Managing the self-fertile Lapins and Sweetheart sweet
cherries in high density systems. Compact Fruit Tree. 35(4):113–114.
5. L a n g, G. A. 2000. Precocious, dwarfing, and productive – how will new cherry
rootstocks impact the sweet cherry industry? Hort Technology. 10:719–725.
6. L a n g, G. A. and D. R. O p h a r d t. 2000. Intensive crop regulation
strategies in sweet cherries. Acta Hort. 514:227–234.
7. L o n g, L. 2001. Cherry training systems: Selection and development. Pacific
Northwest Extension Publication #543. Oregon State University. Corvallis, Oregon.
8. P e r r y, R. 1998. Suggested training strategies for dwarf sweet cherries. Great
Lakes Fruit Growers News. 37(2):45–46.
9. P e r r y, R., G. L a n g, R. A n d e r s e n, L. A n d e r s o n, A.
A z a r e n k o, T. F a c t e a u, D. F e r r e e, A. G a u s, F. K a p p e l, F.
M o r r i s o n, C. R o m, T. R o p e r, S. S o u t h w i c k, G. T e h r a n i and C.
W a l s h. 1996. Performance of the NC-140 cherry rootstock trials in North America.
Compact Fruit Tree. 29:37–56.
10. R o b i n s o n, T. L. 2003. Apple orchard systems. In: D.C. Ferree and I.J.
Warrington (eds.). Apples: Physiology, production and uses. CABI Publishing.
Wallingford, Oxon, United Kingdom.
11. R o b i n s o n, T. L. 2005. Developments in high-density sweet cherry pruning
and training systems around the world. Acta Hort. 667:269–272.
12. R o b i n s o n, T. L., R. L. A n d e r s e n and S. A. H o y i n g. 2004.
Performance of Gisela cherry rootstocks in the Northeastern United States. Acta Hort.
658:231–240.
13. S e a v e r t, C. 1997. Sweet cherry orchard cost analysis: does high-density
pay? Proc. Oregon Hort. Soc. 88:34–42.
14. W e b e r, M. S. 1998. Labor demand and expected returns by different tree
training forms and planting densities in sweet cherry orchards. Acta Hort. 2:419–424.
15. Z a h n, F. G. 1994. Höhengerechter Planzabstand durch Stärkenbezogene
Baumbehandlung. Erwerbsobstbau 8:213–220.
122
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
113–123.
ÞEMAÛGIØ TREÐNIØ POSKIEPIØ PRODUKTYVUMAS JUNGTINIØ
AMERIKOS VALSTIJØ ÐIAURËS RYTUOSE
T. L. Robinson, S. A. Hoying, R. L. Andersen
Santrauka
Treðniø poskiepiai ir formavimo sistemos buvo palyginti atliekant du lauko bandymus
(1999 ir 2002 m.). 1999 metø bandyme ‘Hedelfinger’ veislës treðnë buvo pasodinta su trimis
poskiepiais (Gisela 5, (Gi.5), Gisela 6, (Gi.6) ir MxM.2), o ‘Lapins’ ir ‘Sweetheart’ – su Gi.5 ir
Gi.6. Po 7 metø maþiausi vaismedþiai iðaugo su Gi.5, vidutiniai – su Gi.6 ir didþiausi – su
MXM.2 poskiepiu. Didþiausià ankstyvàjá ir suminá derliø davë vaismedþiai su Gi.5, kiek
maþesná – su Gi.6 ir maþiausià – su MXM.2. Vidutiniðkai didþiausius vaisius subrandino
vaismedþiai su Gi.6, vidutinius – su MXM.2 ir maþiausius – su Gi.5. Ið sodinimo sistemø
didþiausià suminá derliø davë vertikaliosios aðies sistema, kiek maþesná – laiboji verpstë,
V sistema, Marchanto V sistema, ispaniðko krûmo sistema ir centrinë lyderinë sistema.
Suminis derlius daþnai priklausë nuo tankumo, taèiau Marchanto V sistema davë ið esmës
maþesná, negu tikëtasi ið jos tankumo, derliø, o vertikaliosios aðies sistema davë didesná,
negu tikëtasi ið jos tankumo, derliø. 2002 metø lauko bandyme ‘Lapins’, ‘Regina’ ir ‘Hudson’
veislës buvo pasodintos su Mazzard, Gi.12, Gi.5 ir Gi.6 poskiepiais. Po 4 metø vaismedþiai
su Gi.12 buvo tokie pat dideli, kaip su Mazzard, su Gi.6 buvo vidutiniai, o su Gi.5 – ið esmës
maþesni. Didþiausià derliø davë vaismedþiai su Gi.5, kiek maþesná – su Gi.6 ir Gi.12, o
vaismedþiø su Mazzard derlius buvo gerokai maþesnis negu su visais kitais Gisela
poskiepiais. ‘Reginos’ veislës treðniø vaismedþiai su Gi.5 poskiepiu, suformuoti vertikalios
aðies vainikais, ketvirtaisiais metais davë 12 t/ha dideliø treðniø derliø.
Reikðminiai þodþiai: Prunus avium, Gisela poskiepiai, derlius, vaisiø dydis,
formavimo sistema, sodinimo tankumas.
123
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 124–132.
INFLUENCE OF PLANTING SCHEMES AND CROWN
FORMS OF APPLE TREE ON ROOTSTOCK P 60 ON
PRODUCTIVITY AND FRUIT QUALITY
Nobertas USELIS
Lithuanian Institute of Horticulture, LT–54333, Babtai, Kaunas distr.,
Lithuania. E-mail: [email protected]
The experiment of apple tree cv. ‘Auksis’ on rootstock P 60 planting schemes and
crown forms was arranged at the Lithuanian Institute of Horticulture in 2001. Investigations
were carried out in young orchard in 2002–2005. There were investigated fruit trees of
spindle form planted at spacings of 3 x 1.5 m, 3 x 1.25 m and 3 x 1 m; fruit trees of slender
spindle form planted at spacings of 3 x 1.5 m, 3 x 1.25 m, 3 x 1 m and 3 x 0.75 m; fruit trees of
free growing leader form planted at spacing of 3 x 1.5 m and fruit trees of super spindle
form planted at spacing of 3 x 0.75 m. It was established that apple tree cv. ‘Auksis’ on
rootstock P 60 starts fruiting in the third year after planting. In the third-fifth year of
growth significantly lower harvest per tree was produced by super spindles and slender
spindles planted most densely (at spacings of 3 x 0.75 and 3 x 1 m) in comparison to
spindles and free growing leader form planted most sparsely (at spacing of 3 x 1.5 m).
According to the diameter of trunk cross-section area, in most cases spindles and free
growing leader form planted most sparsely (at spacing of 3 x 1.5 m) significantly are the
most vigorous. The biggest fruit yield per unit of area was obtained in the densest orchard
(planted at spacing of 3 x 0.75 m), where fruit trees were trained as slender spindles and
super spindles, and in the orchard planted at spacing of 3 x 1 m, where fruit trees were
trained as spindles. The investigated dwarf orchard constructions in young orchard
influenced significantly neither the average fruit mass, nor fruit diameter.
After the evaluation of orchard constructions from the biological-economical point
of view we suggest to plant apple tree cv. ‘Auksis’ on rootstock P 60 at spacing of 3 x 1 m
and to train as spindles.
Key words: apple trees, P 60, planting schemes, crown forms, growth vigour, yield,
productivity, fruit quality.
Introduction. In the modern commercial apple tree orchards, which planting
and supervision is rather expensive, it is necessary as soon as possible to get rather
abundant, high quality and annual fruit yields. The planted fruit trees must be trained
in such a way that they preserved the desirable crown size and form, also physiological
balance between growth and fruiting; besides, that there would be good illumination
of crown and favourable conditions to obtain the early marketable yield of qualitative
124
fruits. Orchard density, pruning and training directly and indirectly affect the intensity
of fruit tree physiological processes.
Investigations in various countries revealed that fruit quality and yield per fruit
tree and from the unit of area is determined by the number of fruit trees per hectare.
Many authors established that the bigger yield from the area, but the lesser one per
fruit tree is obtained when fruit trees are planted more densely (Deviatov, 1997;
Mika, 1998; Uselis, 2003).
Fruit tree crown form most often is chosen taking into account the planting
scheme. Usually fruit trees are trained as spindles of various modifications. In Poland
fruit trees are trained as spindles when they are planted at spacing of 4 – 5 x 3 – 2 m
and as slender spindles when they are planted at spacing of 3.5 – 3 x 1.5 – 1 m. Very
densely planted fruit trees (3 x 0.8 – 0.5 m) are trained as super spindles or French
axis crowns (Makosz, 1997).
When investigating fruit tree over-ground part biology it was noticed that the
more the branch is leaned over the more it produces fruits. Therefore, when training
the crowns of spindle form, the shoots, which grow at vertical sharp angle, are
being bent horizontally (Forshey et al. 1992; Mika, 1998). Nevertheless, the other
authors noticed that crown form only slightly affected the yield and fruit quality of
apple tree cultivars ‘Jonagold’, ‘Gloster’ and ‘Idared’ on dwarf rootstocks
(Krziewinska, Mika, 1998; Szewcuk, Sosna, 1998).
The aim of investigations is to analyze and to evaluate the influence of planting
schemes and crown forms of apple tree cv. ‘Auksis’ on rootstock P 60 on fruit tree
yield, productivity and fruit quality in young age.
Material and methods. The experiment of apple tree cv. ‘Auksis’ on rootstock
P 60 planting schemes and crown forms was arranged in 2001. Investigations were
carried out in young orchard in 2002–2005.
The scheme of the experiment: 1) spindle crown, planting scheme – 3 x 1.5 m
(2222 trees/ha); 2) slender spindle crown, planting scheme – 3 x 1.5 m
(2222 trees/ha); 3) free growing leader spindle, planting scheme – 3 x 1.5 m
(2222 trees/ha); 4) spindle crown, planting scheme – 3 x 1.25 m (2667 trees/ha);
5) slender spindle crown, planting scheme – 3 x 1.25 m (2667 trees/ha); 6) spindle
crown, planting scheme – 3 x 1 m (3333 trees/ha); 7) slender spindle crown, planting
scheme – 3 x 1 m (3333 trees/ha); 8) super spindle crown, planting scheme –
3 x 0.75 m (4444 trees/ha); 9) slender spindle crown, planting scheme – 3 x 0.75 m
(4444 trees/ha).
The investigation consisted of 4 replications with 5 fruit trees in each, 3 of
them were evaluated. There was evaluated: fruit tree flowering abundance in scores,
where 0 – fruit trees do not flower at all and 5 – fruit trees flower very abundantly;
growth vigour – trunk diameter (cm2) at the height of 0.25 m, yield (kg/fruit tree and
t/ha), fruit tree productivity (kg/cm2), the average fruit mass (g), and fruit diameter
(mm) were measured. The data of investigation were evaluated by Anova.
The changes of meteorological conditions during investigations didn’t influence
significantly the results, with the exception of 2004 when strong frosts in May
destroyed two thirds of apple tree blossoms.
125
Results. F l o w e r i n g a b u n d a n c e a n d y i e l d. ‘Auksis’ on dwarf
rootstock P 60 started abundant flowering in the third year in the orchard. According
to the average data of three years, the abundance of fruit tree flowering almost
didn’t depend on both orchard density and crown form (Table 1). Nevertheless,
fruit trees of spindle form planted at spacing of 3 x 1 m flowered most abundantly in
comparison with super spindles, which grew most densely.
T a b l e 1. Flowering abundance and yield of apple tree cv. ‘Auksis’.
Babtai, 2003–2005
1
l e n t e l ë. ‘Auksio’ veislës obelø þydëjimo gausumas ir derlius. Babtai, 2003–2005 m.
Orchard construction
Sodo konstrukcija
Flowering abundance, scores
Þydëjimo gausumas balais
Spindle
Paprastoji verpstë,
Yield, kg/fruit trees
Derlius, kg/vaism.
4.3
11.79
4.3
10.37
4.4
13.14
4.6
11.50
4.4
9.76
4.7
10.23
4.4
8.61
4.0
7.51
4.3
8.61
0.68
3.091
3 x 1.5 m
Slender spindle
Laiboji verpstë, 3 x 1.5 m
Free growing leader / Laisvai augantis
lyderinis vainikas, 3 x 1.5 m
Spindle
Paprastoji verpstë, 3 x 1.25 m
Slender spindle
Laiboji verpstë, 3 x 1.25 m
Spindle
Paprastoji verpstë, 3 x 1 m
Slender spindle
Laiboji verpstë, 3 x 1 m
Super spindle
Superverpstë, 3 x 0.75 m
Slender spindle
Laiboji verpstë, 3 x 0.75 m
LSD05 / R05
The average three-year fruit yield per fruit tree revealed a tendency that more
densely planted fruit trees produced poorer yield in comparison to these, which
grew more sparsely (Table 1). Most densely (3 x 0.75 m and 3 x 1 m) growing super
spindles trees and slender spindles trees yielded significantly worse than spindles
and free growing leaders trees planted most sparsely (3 x 1.5 m).
G r o w t h v i g o u r a n d p r o d u c t i v i t y. According to trunk
cross-section area, spindles and free growing leaders trees planted most sparsely
(3 x 1.5 m) in most cases were the most vigorous (Table 2). The most densely
(3 x 0.75 m) growing fruit trees most often were significantly more slender in
comparison to these, which grew more sparsely.
Fruit trees of spindle form planted at spacings of 3 x 1 m and 3 x 1.25 and these
of free growing leader form planted most sparsely (at spacing of 3 x 1.5 m) are the
most productive (Table 2). Slender spindles growing at spacing of 3 x 1 m and super
spindles growing at spacing of 3 x 0.75 m are significantly the least productive.
126
T a b l e 2. Growth vigour and productivity of apple tree cv. ‘Auksis’.
Babtai, 2003–2005
2
l e n t e l ë.
‘Auksio‘ veislës obelø augumas ir produktyvumas. Babtai, 2003–2005 m.
Orchard construction
Sodo konstrukcija
Spindle
Trunk cross-section area in Productivity in 2003–2005
2005 / Kamienëlio skerspjûvio Produktyvumas 2003–2005 m.,
2
plotas 2005 m., cm
kg/cm2
19.64
1.80
Paprastoji verpstë,
3 x 1.5 m
Slender spindle
Laiboji verpstë, 3 x 1.5 m
Free growing leader
Laisvai augantis lyderinis vainikas,
1.94
18.37
2.15
16.25
2.12
15.09
1.94
15.21
2.02
16.14
1.60
13.31
1.69
13.63
1.90
2.508
0.204
3 x 1.5 m
Spindle
Paprastoji verpstë,
16.02
3 x 1.25 m
Slender spindle
Laiboji verpstë, 3 x 1.25 m
Spindle
Paprastoji verpstë, 3 x 1 m
Slender spindle
Laiboji verpstë, 3 x 1 m
Super spindle
Superverpstë, 3 x 0.75 m
Slender spindle
Laiboji verpstë, 3 x 0.75 m
LSD05 / R05
Y i e l d p e r a r e a a n d f r u i t q u a l i t y. From the point of
economy, it is very important what yield is being gathered per unit of area. In the
first year of fruiting (2003) the most densely (at spacing of 3 x 0.75 m) planted
orchard of slender spindles and orchard of spindles planted at spacing of 3 x 1 m
yielded significantly better (Table 3). During the second year of fruiting (2004) because
of the strong spring frosts the yield wasn’t big and did not depend on fruit tree
planting scheme or their form, with the exception of more abundant yielding of free
growing leaders. In the third year of fruiting, when the orchard yielded especially
abundantly, the most densely planted orchard yielded significantly the most abundantly
not dependently on crown form and in most cases spindles planted at spacing of
3 x 1 m yielded significantly better (Table 3).
According to the average data of three years significantly the biggest fruit yield
per area unit was obtained in the densest orchard (3 x 0.75 m), where fruit trees
were trained as slender spindles and super spindles. Dwarf orchard construction,
where fruit trees were planted at spacing of 3 x 1 m and trained as spindles, was
distinguished for abundant yield also. In the case of this orchard construction, the
productivity per unit of area significantly didn’t differ from the productivity of the
orchard planted most densely and orchard, where spindles were planted slightly
more sparsely (3 x 1.25 m). Fruit trees planted most sparsely (3 x 1.5 m) or fruit
trees planted at similar spacing, but trained as slender spindles, produced significantly
smaller yield per unit of area in comparison to spindles planted at spacing of 3 x 1 m.
127
In the years of abundant yielding the average fruit mass depended neither on
fruit tree density, nor on crown form (Table 4). Only it was observed a tendency
that most densely planted slender spindles trees produced smaller fruits.
T a b l e 3. Yield of apple tree cv. ‘Auksis’. Babtai, 2003–2005
3
l e n t e l ë. ‘Auksio‘ veislës obelø derlius, t/ha. Babtai, 2003–2005 m.
Orchard construction
Average
2003
2004 2005
Spindle / Paprastoji verpstë, 3 x 1.5 m
23.40
7.87 47.33
26.20
Slender spindle / Laiboji verpstë, 3 x 1.5 m
18.40 10.51 40.21
23.04
Free growing leader / Laisvai augantis lyderinis vainikas, 3 x 1.5 m
19.64 19.00 48.94
29.19
Spindle / Paprastoji verpstë, 3 x 1.25 m
23.98 13.52 54.51
30.67
Slender spindle / Laiboji verpstë, 3 x 1.25 m
18.54 11.87 47.72
26.04
Spindle / Paprastoji verpstë, 3 x 1 m
31.06 12.13 59.13
34.11
Slender spindle / Laiboji verpstë, 3 x 1 m
27.03
6.70 52.32
28.68
Super spindle / Superverpstë, 3 x 0.75 m
23.42 12.27 64.40
33.36
Slender spindle / Laiboji verpstë, 3 x 0.75 m
37.55
8.75 68.48
38.26
LSD05 / R05
8.978 6.262 8.165
5.389
Sodo konstrukcija
Vidutiniškai
T a b l e 4. Fruit mass of apple tree cv. ‘Auksis’. Babtai, 2003–2005
4
l e n t e l ë. Vaisiø masë, g. Babtai, 2003–2005 m.
Orchard construction
Average
2003
2005
Spindle / Paprastoji verpstë, 3 x 1.5 m
Slender spindle / Laiboji verpstë, 3 x 1.5 m
Free growing leader / Laisvai augantis lyderinis vainikas, 3x1.5 m
Spindle / Paprastoji verpstë, 3 x 1.25 m
Slender spindle / Laiboji verpstë, 3 x 1.25 m
Spindle / Paprastoji verpstë, 3 x 1 m
Slender spindle / Laiboji verpstë, 3 x 1 m
Super spindle / Superverpstë, 3 x 0.75 m
Slender spindle / Laiboji verpstë, 3 x 0.75 m
146
151
151
147
151
146
131
154
141
125
136
120
122
133
119
125
124
114
135.5
143.5
135.5
134.5
142.0
132.5
128.0
139.0
127.5
LSD05 / R05
22.5
19.8
16.3
Sodo konstrukcija
Vidutiniškai
When fruits were sorted into marketable classes it was established that in the
years of the average yielding (2003 and 2005) even 91–94% of fruits according to
their diameter corresponded to extra class requirements (Table 5). Fruit diameter
significantly depended neither on fruit tree density, nor on the form of their crown.
It was observed a tendency that there are more fruits of I and II class in more dense
variants. The amount of unsorted fruits reached only 0.3–1.8% and strongly varied
among different variants.
128
T a b l e 5. Distribution of apples according to diameter, %. Babtai,
2003–2005
5
l e n t e l ë.
Obuoliø pasiskirstymas pagal skersmená, %. Babtai, 2003–2005 m.
Extra class
I and II class
Unsorted
60–64 mm
up to 60 mm
93.0
6.5
0.5
93.4
5.5
1.1
93.8
4.4
1.8
94.2
5.1
0.7
94.0
5.4
0.6
91.5
7.2
1.3
91.3
8.4
0.3
94.3
5.1
0.6
91.2
7.4
1.4
5.51
1.92
0.81
Orchard construction
Ekstra klasë
Sodo konstrukcija
65 mm and more
65 mm ir daugiau
Spindle
Paprastoji verpstë,
I ir II klasë
Nerûðiniai
iki 60 mm
3 x 1.5 m
Slender spindle
Laiboji verpstë, 3 x 1.5 m
Free growing leader / Laisvai
augantis lyderinis vainikas, 3x1.5 m
Spindle
Paprastoji verpstë, 3 x 1.25 m
Slender spindle
Laiboji verpstë, 3 x 1.25 m
Spindle
Paprastoji verpstë, 3 x 1 m
Slender spindle
Laiboji verpstë, 3 x 1 m
Super spindle
Superverpstë, 3 x 0.75 m
Slender spindle
Laiboji verpstë, 3 x 0.75 m
LSD05 / R05
Discussion. Taking into account economical, agroclimatic and soil conditions
it is very important in every country to choose the suitable combinations of cultivars
and rootstocks and to create the optimal constructions of modern orchards. In Poland
E. Makosz (1997) states that it is more economical to exploit orchards, which density
is 2000–3000 tree/ha, than more sparse – 500–1200 tree/ha. Other authors are of
similar opinion (Groot, 1995; Mika, 1998; Meljnik, Shestopalj, 1998; Klochko, 1999).
Our investigations showed that in the case of combination of cv. ‘Auksis’ and dwarf
rootstock P 60 already in the third year after planting dependently on orchard
constructions there was obtained high quality fruit yield (18.4–37.6 t/ha). Similar
results with apple tree cv. ‘Ðampion’ were obtained by D. Kviklys, N. Kviklienë
(2005). Therefore, under Lithuanian agroclimatic conditions it is also possible to
obtain abundant and qualitative fruit yields already in the young orchard, when the
combination of cultivar and rootstock is suitable.
The investigations showed that in the third-fifth year in the orchard fruit trees
flowered abundantly and the abundance of flowering depended almost neither on
crown form, nor on planting schemes. The exception was only spindles planted at
spacing of 3 x 1 m (3333 trees/ha), which flowered most abundantly (4.7 scores),
and most densely (3 x 0.75 m, 4444 trees/ha) planted super spindles, which flowering
was the worst (4.0 scores). Nevertheless, the investigations of photosynthetic
pigments carried out in this experiment by Ðabajevienë et al. (2005) showed that
129
when apple tree cv. ‘Auksis’ on rootstock P 60 were densified from 2222 trees/ha up
to 4444 trees/ha the amount of photosynthesis pigments and their ratio in apple tree
leaves was suitable and crown forms in young age didn’t inhibit photosynthesis.
As well as in the investigations of the other authors (Chromenko, 2000;
Slowinski, Dziuban, 2002), in this experiment also it was observed that when
densifying fruit trees per unit of area both their growth vigour and productivity
decreased.
In most cases when fruit trees were densified from 2222 trees/ha up to
4444 trees/ha they grew and yielded significantly worse. Nevertheless, it is most
important to obtain big yields per unit of area and good quality fruits. According to
the data of three years, significantly the biggest yield per area was obtained when
fruit trees were planted most densely (4444 trees/ha) and trained as slender spindles
and super spindles. In young age spindles trees, which were planted more sparsely
(3333 trees / ha), was distinguished also for abundant flowering and abundant yield.
The investigation showed that in young age spindles with more branches have an
advantage over slender spindles.
When densifying dwarf orchards and increasing the productivity per area it is
very important to guarantee good fruit quality too. Investigations showed that
according to the average data, during the first three years of yielding neither fruit
mass nor fruit diameter depended on neither fruit tree density nor crown forms. It
may be that when orchard will grow older fruit quality will not become worse even
in the densest variants, if the previsioned fruit tree forms will be preserved taking
into account fruit tree planting distances.
The complex evaluations of the investigated orchard constructions from the
biological-economical point of view revealed that it is enough to plant apple tree cv.
‘Auksis’ on rootstock P 60 at spacing of 31 m (3333 trees/ha) and to train fruit trees
as spindles.
Conclusions. 1. Apple tree cv. ‘Auksis’ on dwarf rootstock P 60 start abundant
flowering and fruiting in the third year after planting.
2. According to the average three-year data (in the third-fifth years of growth)
fruit trees of all constructions flower in orchard abundantly, but the flowering of
spindles planted at spacing of 3 x 1 m is the biggest one.
3. The yielding of super spindles and slender spindles trees planted most densely
at spacings of 3 x 0.75 m and 3 x 1 m is the worst in comparison to the yielding of
spindles and free growing leaders trees planted most sparsely at spacing of 3 x 1.5 m.
4. According to the trunk cross-section area, in most cases spindles and free
growing leaders trees planted most sparsely at spacing of 3 x 1.5 m are significantly
the most vigorous.
5. Spindles trees planted at spacings of 3 x 1 m and 3 x 1.25 m and free
growing leaders trees planted most sparsely at spacing of 3 x 1.5 m are the most
productive. Slender spindles trees growing at spacing of 3 x 1 m and super spindles
trees growing at spacing of 3 x 0.75 m were significantly the least productive.
6. Significantly the biggest fruit yield per unit of area was obtained in the densest
orchard of slender spindles and super spindles trees planted at spacing of 3 x 0.75 m,
and in orchard of spindles trees planted at spacing of 3 x 1 m.
130
7. The investigated dwarf orchard constructions in the young orchard influence
significantly neither the average fruit mass nor fruit diameter.
8. After the evaluation of orchard constructions from the biological-economical
point of view we suggest to plant apple tree cv. ‘Auksis’ on rootstock P 60 at spacing
of 3 x 1 m and to train as spindles.
Acknowledgement. This work was partly supported by Lithuanian State Science
and Studies Foundation.
Gauta
2006 06 25
Parengta spausdinti
2006 07 26
References
1. C h r o m e n k o V. V. Bases of productivity of cultivar, tree and plantation. /
History, present and perspective of Russian horticulture. I. F. Kashin (eds.). Moscow,
2000. P. 279–290.
2. D e v i a t o v A. S. Productivity of apples on dwarf rootstocks at dense
planting system // Dwarf apple rootstocks in horticulture. 1997. P. 92–93.
3. F o r s h e y C. G., E l f o v i n g D. C., S t e b b i n s R. L. Training
and pruning apple and pear trees. Michigan, 1992. 160 p.
4. G r o o t M. J. Economic calculations on high – density plantings // Ann. Rep.
fruit Res. Station for 1994. Wilhelminadorp, 1995. P. 74–77.
5. K l o c h k o P. Yield of apple trees on clonal rootstocks in different types of
intensive orchards under irrigation in the Southern Ukraine // Proc. Apple rootstocks for
intensive orchards. Warszawa, 1999. P 57–59.
6. K v i k l y s D., K v i k l i e n ë N. Performance of apple trees in the young
orchard, depending on the quality of planting material // Fruit – growing, Samohvalovichi,
2005. V. 17(2). P. 67–71.
7. K r z e w i n s k a D., M i k a A. Effect of planting density and canopy form
on yield and fruit quality of cvs. Jonagold, Gloster and Idared // Proc. XXXVII horticultural
conference Skierniewice, 1998. P. 440–443.
8. M a k o s z E. Economical evaluation of different apple planting schemes //
Strategy of fruit growing development in Poland until 2010. Lublin, 1997. P. 187–190.
9. M e l j n i k A. V., S h e s t o p a l j A. H. State and tendencies of Ukrainian
horticulture // Proc. Horticulture in Central and Eastern Europe. 1998. P. 157–172.
10. M i k a A. Orchard models of XXI century // Proc. XXXVII horticultural
conference Skierniewice, 1998. P. 75–76.
11. S l o w i n s k i A., D z i u b a n R. Growth, cropping and fruit quality of
‘Gloster’ and ‘Elstar’ apple trees at two planting densities // Sodininkystë ir darþininkystë.
Babtai, 2002. V. 21(3). P. 113–117.
12. S z e w c u k A., S o s n a I. Development of model of intensive apple orchard
at Dalnego Slaska climatic conditions // Proc. Horticulture in Central and Eastern Europe.
Lublin, 1998. P. 213–220.
13. Ð a b a j a v i e n ë G., U s e l i s N., D u c h o v s k i s P. Investigation
of photosynthesis pigments of cultivar ‘Auksis’ in high density orchards of different
contruction // Sodininkystë ir darþininkystë. Babtai, 2005. V. 24(4). P. 57–64.
131
14. U s e l i s N. Growth and productivity of dwarf apple trees in bearing orchards
of various constructions // Sodininkystë ir darþininkystë. Babtai, 2003. V. 22(1). P. 3–13.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
124–132.
OBELØ SU P 60 POSKIEPIU SODINIMO SISTEMØ IR VAINIKO FORMØ
ÁTAKA VAISMEDÞIØ PRODUKTYVUMUI IR VAISIØ KOKYBEI
N. Uselis
Santrauka
‘Auksio‘ veislës obelø su P 60 poskiepiu sodinimo schemø ir vainiko formø bandymas
árengtas 2001 m. Lietuvos sodininkystës ir darþininkystës institute. Tyrimai atlikti jauname
sode 2002–2005 m. Tirti paprastosios verpstës formos vaismedþiai, pasodinti 3 x 1,5 m,
3 x 1,25 m ir 3 x 1 m atstumais, laibosios verpstës formos vaismedþiai, pasodinti 3 x 1,5 m,
3 x 1,25 m, 3 x 1 m ir 3 x 0,75 m, laisvai auganèios lyderinës formos vaismedþiai, pasodinti
3 x 1,5 m, ir superverpstës formos vaismedþiai, pasodinti 3 x 0,75 m atstumais. Nustatyta,
kad ’Auksio‘ veislës obelys su þemaûgiu P 60 poskiepiu gausiai þydëti ir derëti pradeda
treèiaisiais po sodinimo metais. Treèiaisiais–penktaisiais augimo metais ið esmës
prasèiausiai dera tankiausiai – 3 x 0,75 m ir 3 x 1 m atstumais – auginami superverpstës ir
laibosios verpstës vaismedþiai, palyginti su reèiausiai – 3 x 1,5 m atstumais – pasodintais
paprastosios verpstës ir laisvai auganèios lyderinës formos vaismedþiais. Pagal kamienëlio
skerspjûvio plotà daugeliu atvejø reèiausiai pasodinti (3 x 1,5 m) paprastosios verpstës ir
laisvai auganèios lyderinës formos vaismedþiai yra ið esmës augiausi. Ið esmës didþiausias
vaisiø derlius ið ploto vieneto gautas tankiausiame – 3 x 0,75 m atstumais pasodintame –
sode, kur vaismedþiai suformuoti laibosios verpstës ir superverpstës vainikais, ir 3 x 1 m
atstumais pasodintame sode, kur vaismedþiai suformuoti paprastosios verpstës formos
vainikais. Tirtos jauno þemaûgio sodo konstrukcijos neturi esminës átakos nei vaisiø
vidutinei masei, nei jø pasiskirstymui pagal skersmená. Ávertinus sodo konstrukcijas
biologiniu ir ûkiniu poþiûriu, siûloma ‘Auksio‘ obelis su þemaûgiu P 60 poskiepiu sodinti
3 x 1 m atstumais ir vaismedþius formuoti paprastosios verpstës formos vainikais.
Reikðminiai þodþiai: augumas, derlingumas, obelys, P 60, produktyvumas, sodinimo
sistemos, vainiko formos, vaisiø kokybë.
132
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 133–143.
INFLUENCE OF PLANTING SCHEMES AND CROWN
FORMS ON PRODUCTIVITY AND FRUIT QUALITY OF
APPLE TREES ON ROOTSTOCK P 22
Nobertas USELIS, Gintarë ÐABAJEVIENË,
Pavelas DUCHOVSKIS
Lithuanian Institute of Horticulture, LT–54333, Babtai, Kaunas distr.,
Lithuania. E-mail: [email protected]
The experiment of apple tree cv. ‘Auksis’ on rootstock P 22 planting schemes and
crown forms was arranged at the Lithuanian Institute of Horticulture in 2001. Investigations
were carried out in young orchard in 2002–2005. There were investigated fruit trees of
spindle form planted at spacing of 3 x 1.5 m; fruit trees of slender spindle form planted at
spacing of 3 x 0.5 m and 3 x 1 m; fruit trees of free growing leader form planted at spacing
of 3 x 1 m and fruit trees of super spindle form planted at spacing of 3 x 0.75 m, 3 x 0.5 m and
3 x 0.25 m. Slender spindles and super spindles also were investigated in V system.
It was established that apple tree cv. ‘Auksis’ on super dwarf rootstock P 22 start
abundant flowering already in the second year after planting. Fruit tree yield in young age
depended on planting schemes and almost didn’t depend on canopy form. Most sparsely
(3 x 1 m) planted fruit trees produced the biggest yield per tree – 3.98–4.57 kg. Super
spindles planted most densely in V system and super spindles planted at spacings of
3 x 0.25 m and 3 x 0.5 m were distinguished for the biggest average yield per unit of area,
correspondingly 32.82 t/ha and 26.14–27.54 t/ha. The smallest yield per unit of area was
obtained in most sparsely (3 x 1 m) planted variants (13.26–15.22 t/ha). Both the average
fruit mass and fruit size according to the diameter of the most densely (3 x 0.25 m) planted
fruit trees were significantly smaller in comparison to the fruits of more sparsely grown
fruit trees.
After the complex evaluation of orchard constructions from the biological-economical
point of view we suggest to plant apple tree cv. ‘Auksis’ on super dwarf rootstock P 22 at
spacing of 3 x 0.5 m (6667 trees / ha) and to train as super spindles.
Key words: apple trees, P 22, planting schemes, canopy forms, growth vigour, yield,
productivity, fruit quality.
Introduction. The growing of dessert apples in Lithuania is one of the priority
commercial horticulture trends. Therefore taking into account climatic and economical
conditions in the country the technologies of dessert fruit growing are being constantly
improved. The main purpose is to create the technologies, which allow cultivating
high quality dessert apple yields. This is especially important, because Lithuania
entered EU and competition in fruit market became extremely ardent. One of the
133
most important questions in commercial fruit growing is to choose properly the
combination of cultivar and rootstock ant to introduce the optimal orchard
construction. In the last century the transition from the vigorous and sparsely planted
orchards to much more intensive densely planted semi-dwarf and dwarf orchards
took place (Uselis, 2002). Nevertheless, when intensifying horticulture various
investigators obtain different results. Slowinski and Dziuban (2002) investigations
showed that when orchards were densified from 2020 to 6040 trees / ha fruit tree
productivity decreased, but the yield per unit of area increased and fruit quality
didn’t worsen.
Intensive orchards were investigated by many scientists in various countries
(Sansavini et al., 1980; Ystaas et al., 1994; Callesen, 1995; Widmer and Krebs, 2001;
Szczygel et al., 2000). Lakso and Robinson (1997) established that the yield of fruit
trees was positively related to leaf area and light interception. There are a lot of
opinions that when fruit trees are densified too much fruit quality very worsen because
of the insufficient illumination (Mika et al., 2000; Ystaas et al., 1994; LicznarMalanczuk, 2001; Sadowski et al. 2001).
The aim of the investigation is to evaluate the influence of apple tree cv. ‘Auksis’
on rootstock P 22 planting schemes canopy forms on fruit tree yield, productivity
and fruit quality in young age.
Material and methods. The experiment of apple tree cv. ‘Auksis’ on rootstock
P 22 planting schemes and canopy forms was arranged in 2001. Investigations were
carried out in young orchard in 2002–2005.
The scheme of the experiment: 1) spindle, planting scheme – 3 x 1 m
(3333 trees/ha); 2) slender spindle, planting scheme – 3 x 1 m (3333 trees/ha); 3)
free growing leader form, planting scheme – 3 x 1 m (333 trees/ha); 4) super spindle,
planting scheme – 3 x 0.75 m (4444 trees/ha); 5) slender spindle, planting scheme –
3 x 0.75 m (4444 trees/ha); 6) super spindle, planting scheme – 3 x 0.5 m
(6667 trees/ha); 7) super spindle in V system, planting scheme – 3 x 0.5 m
(6667 trees/ha); 8) slender spindle in V system, planting scheme – 3 x 0.5 m
(6667 trees/ha); 9) super spindle, planting scheme – 3 x 0.25 m (13 333 trees/ha);
10) super spindle in V system, planting scheme – 3 x 0.25 m (13333 trees/ha).
The investigation consisted of 4 replications with 5 fruit trees in each, 3 of
them were accounting. There was evaluated: fruit tree flowering abundance in scores,
(0 – fruit trees do not flower at all and 5 – fruit trees flower very abundantly); trunk
diameter (cm2) – at the height of 0.25 m, yield (kg/fruit tree and t/ha), fruit tree
productivity (kg/cm2 of trunk cross section area (TCSA), the average fruit mass
(g), and fruit diameter (mm). The data of investigation were evaluated by ANOVA
statistical program.
The changes of meteorological conditions during investigations didn’t influence
significantly the means, which were being analyzed, with the exception of 2004
when strong frosts in May destroyed two thirds of apple tree blossoms.
Results. Flowering abundance and yield. ‘Auksis’ on super dwarf rootstock
P 22 started abundant flowering already in the second year after planting. Even
though most abundantly apple trees flowered in the fifth year of growth, the average
flowering abundance during 4 years was very high and reached 4–4.4 scores
134
(Table 1). The abundance of fruit tree flowering significantly depended neither on
planting schemes, nor on canopy form.
T a b l e 1. Flowering abundance and yield of apple tree cv. ‘Auksis’
on rootstock P 22, 2002–2005
1
l e n t e l ë.
’Auksio‘ veislës obelø su P 22 poskiepiu þydëjimo gausumas ir
derlius 2002–2005 m.
Flowering abundance, scores
Orchard construction
Sodo konstrukcija
Vidutinis derlius, kg/vaism.
4.3
3.98
4.2
4.27
4.4
4.57
4.2
4.24
4.4
4.01
4.4
3.92
4.1
3.56
4.4
3.26
4.0
2.06
4.1
2.46
0.61
1.192
Spindle
Paprastoji verpstë,
Averige yield, kg/trees
Þydëjimo gausumas balais
3x1m
Slender spindle
Laiboji verpstë, 3 x 1 m
Free growing leader
Laisvai augantis lyderinis vainikas,
3x1m
Super spindle
3 x 0.75 m
Slender spindle
Laiboji verpstë, 3 x 0.75 m
Super spindle
Superverpstë, 3 x 0.5 m
Super spindle, V system
Superverpstë, V forma, 3 x 0.5 m
Slender spindle
Laiboji verpstë, 3 x 0.5 m
Super spindle
Superverpstë, 3 x 0.25 m
Super spindle, V system
Superverpstë, V forma, 3 x 0.25 m
LSD05 / R05
Superverpstë,
The average four-year fruit yield per fruit tree almost didn’t depend on fruit tree
canopy form (Table 1). Investigations showed that fruit trees yield depended on
planting schemes. Fruit trees planted most sparsely (3 x 1 m) yielded best of all
(3.98–4.57 kg / trees). When densifying fruit trees their yield although not significantly
decreased. Only most densely (3 x 0.25 m) planted fruit trees yielded significantly
worst of all (2,06–2,46 kg / trees) (Table 1).
F r u i t t r e e g r o w t h v i g o u r a n d p r o d u c t i v i t y.
According to the diameter of trunk cross-section area, fruit trees planted most sparsely
(3 x 1 m and 3 x 0.75 m) at the end of investigation were the most vigorous
(Table 2). The most densely (3 x 0.25 m) planted fruit trees grew significantly
weakly of all. Also in most cases fruit trees planted at spacing of 3 x 0.5 m grew
significantly worse in comparison to these, which grew more sparsely.
Fruit trees grown most densely (3 x 0.25 m) significantly were the most
productive (Table 2). Fruit tree productivity didn’t depend on canopy form and in
most cases didn’t depend on planting distances when fruit trees were planted at
spacing of 3 x 0.5 m and more sparsely.
135
T a b l e 2. Growth vigour and productivity of apple tree cv. ‘Auksis’
on rootstock P 22, 2003–2005
2
l e n t e l ë.
’Auksio‘ veislës obelø su P 22 poskiepiu augumas ir produktyvumas
2003–2005 m.
Trunk cross-section area
(TCSA), 2005
Orchard construction
Sodo konstrukcija
Spindle
Paprastoji verpstë,
Productivity, 2002–2005,
kg/cm2 of TCSA
Kamienëlio skerspjûvio plotas
2
(KSP) 2005 m., cm
Produktyvumas 2002–2005 m.,
kg/cm2 KSP
9.56
2.40
11.13
2.61
10.70
2.34
10.18
2.40
10.52
2.62
8.88
2.26
8.05
2.26
9.30
2.85
7.20
3.50
7.67
3.11
1.523
0.871
3x1m
Slender spindle
Laiboji verpstë, 3 x 1 m
Free growing leader
Laisvai augantis lyderinis vainikas,
3x1m
Super spindle
3 x 0.75 m
Slender spindle
Laiboji verpstë, 3 x 0.75 m
Super spindle
Superverpstë, 3 x 0.5 m
Super spindle, V system
Superverpstë, V forma, 3 x 0.5 m
Slender spindle
Laiboji verpstë, 3 x 0.5 m
Super spindle
Superverpstë, 3 x 0.25 m
Super spindle, V system
Superverpstë, V forma, 3 x 0.25 m
LSD05 / R05
Superverpstë,
Y i e l d p e r a r e a a n d f r u i t q u a l i t y. The first yield in the
second year after planting strongly depended on fruit tree density (Table 3). The
least yield per unit of area was produced by the most sparsely planted fruit trees
(8.17–9.61 t/ha). When the number of fruit trees per hectare increased, the yield of
orchard increased also. The doubling of the number of fruit trees per unit of area
produced significantly bigger yield, and the biggest yield was obtained when the
orchard was planted most densely (3 x 0.25 m) (23.34–26.86 t/ha). It was observed
that in young age fruit tree forms didn’t influence significantly orchard yield.
Ne x t year, after the big first yield, the second yield was smaller and very
varied. In most cases there weren’t significant differences of yielding among the
different variants (Table 3).
In 2004 during apple tree flowering there were strong frosts, which injured
most blossoms and therefore fruit yield was very poor. Next year the biggest apple
yield was obtained in the ex periment (33–80 t/ha). In the most productive year the
poorest yield was obtained from the most sparsely (3 x 1 m) planted orchard
(Table 3). When increasing fruit tree number per unit of area, orchard yield increases
also and when orchard is planted at spacing of 3 x 0.5 m and 3 x 0.25 m the increase
136
of yield is significant. Most densely planted super spindles in V system were
distinguished for the biggest yield (80 t/ha). Super spindles planted at spacing of
3 x 0.25 m and 3 x 0.5 m also were distinguished for very big yield.
T a b l e 3. The yield of apple tree cv. ‘Auksis’ on rootstock P 22,
2002–2005
3
l e n t e l ë. ’Auksio’ veislës obelø su P 22 poskiepiu derlius, t/ha 2002–2005 m.
Yield / Derlius, t/ha
Orchard construction
Sodo konstrukcija
Spindle
Paprastoji verpstë,
average
2002
2003
2004
2005
9.61
5.83
4.51
33.11
13.26
9.32
8.69
4.40
34.45
14.22
8.17
11.58
4.60
36.55
15.22
11.23
8.29
5.30
50.58
18.85
10.56
12.33
5.41
42.98
17.82
14.68
19.96
6.90
63.00
26.14
16.50
15.05
7.20
56.15
23.72
14.85
14.88
7.01
50.12
21.72
26.86
11.21
8.98
63.10
27.54
23.34
18.36
9.25
80.33
32.82
5.057
10.630
4.011
18.251
9.251
vidutiniškai
3x1m
Slender spindle
Laiboji verpstë, 3 x 1 m
Free growing leader
Laisvai augantis lyderinis vainikas,
3x1m
Super spindle
Superverpstë, 3 x 0.75 m
Slender spindle
Laiboji verpstë, 3 x 0.75 m
Super spindle
Superverpstë, 3 x 0.5 m
Super spindle, V system
Superverpstë, V forma, 3 x 0.5 m
Slender spindle
Laiboji verpstë, 3 x 0.5 m
Super spindle
Superverpstë, 3 x 0.25 m
Super spindle, form V
Superverpstë, V system, 3 x 0.25 m
LSD05 / R05
The average yield data during four years showed that like in the most productive
year the least yield per unit of area was obtained in the most sparsely planted orchards
(13.26–15.22 t/ha) (Table 3). In most cases significantly more abundantly yielded
the orchard planted at spacing of 3 x 0.5 m and 3 x 0.25 m. The most densely
planted super spindles trained in V system (32.82 t/ha) and super spindles planted at
spacing of 3 x 0.25 m and 3 x 0.5 m (26.14–27.54 t/ha) were distinguished for the
most abundant average yield.
Investigating fruit quality it was established that in very productive years
(2002–2005) the average fruit mass was smaller than that in not productive 2003
(Table 4). In the first year of yielding the average fruit mass depended neither on
crown form, nor on planting scheme. Was observed the tendency that the most
densely grown fruit trees produced the smallest fruits. Super spindles planted at
spacing of 3 x 0.5 m were distinguished for significantly bigger fruits than these of
the same fruit trees planted twice more densely (3 x 0.25 m). In the extremely
productive year 2005 the average fruit mass significantly depended neither on planting
schemes, nor on canopy forms.
137
T a b l e 4. Fruit mass, g. 2002–2005
4
l e n t e l ë. Vaisiø masë, g 2002–2005 m.
Fruit mass / Vaisiø masë, g
Orchard construction
Sodo konstrukcija
Spindle
Paprastoji verpstë,
average
2002
2003
2005
118.8
152.5
128.3
133.2
126.8
153.2
133.7
137.9
131.8
139.5
129.0
133.4
127.3
143.0
128.5
132.9
117.0
139.8
135.6
130.8
141.5
137.0
121.9
133.5
128.8
139.0
121.6
129.8
128.3
138.5
123.5
130.1
105.8
130.2
120.4
118.8
106.5
131.5
124.0
120.7
29.93
18.84
14.52
11.71
vidutiniškai
3x1m
Slender spindle
Laiboji verpstë, 3 x 1 m
Free growing leader
Laisvai augantis lyderinis vainikas,
3x1m
Super spindle
3 x 0.75 m
Slender spindle
Laiboji verpstë, 3 x 0.75 m
Super spindle
Superverpstë, 3 x 0.5 m
Super spindle, V system
Superverpstë, V forma, 3 x 0.5 m
Slender spindle
Laiboji verpstë, 3 x 0.5 m
Super spindle
Superverpstë, 3 x 0.25 m
Super spindle, V system
Superverpstë, V forma, 3 x 0.25 m
LSD05 / R05
Superverpstë,
The average three year data showed that the average fruit mass was significantly
smaller only of the most densely (3 x 0.25 m) planted fruit trees (Table 4). In the
other orchard constructions the mass of fruits was almost the same.
The data of fruit calibration showed that in most cases the tendency prevailed
that spindles and slender spindles planted most sparsely produced the fruits of the
biggest diameter (Table 5). The most densely (3 x 0.25 m) grown fruit trees produced
significantly the smallest fruits.
Discussion. When intensifying commercial fruit growing further on, it is very
important that the optimal rootstock, which corresponds to the agroclimatic conditions
of the country, would be chosen for the main commercial apple tree cultivars and
the rational construction of the commercial orchard would be created. The average
vigorous apple tree cv. ‘Auksis’ was chosen for the investigations and it was expected
to densify orchard maximally and to obtain the abundant and good quality fruit yields.
Investigations showed that apple tree cv. ‘Auksis’ on super dwarf rootstock
P 22 flowered abundantly already in the second year after planting. According to the
average four-year data, flowering abundance depended neither on fruit tree canopy
form, nor on planting schemes, but fruit trees were of different growth vigour. It
was established that according to trunk cross-section area the most sparsely
(3 x 1 m and 3 x 0.75 m) grown fruit trees were the most vigorous, and the most
densely (3 x 0.25 m) planted fruit trees grew significantly less. The similar results
138
were obtained by other researchers also (Deviatov, 1997; Mika, 1998; Chromenko,
2000; Uselis, 2003). Therefore, when the orchard is densified, even though fruit
trees flower abundantly, their growth vigour and fruit yield per fruit tree decreases.
On the other hand, investigations carried out by Ðabajevienë et al. (2006) showed
that in this experiment, in all combinations of apple tree cv. ‘Auksis’ on rootstock
P 22 orchard densities (3 x 1 m; 3 x 0.75 m; 3 x 0.5 m; 3 x 0.25 m) and canopy
forms there was enough of photosynthesis pigments and ratio of chlorophylls a/b
were sufficient and did not inhibit photosynthesis. Consequently, there is the foundation
for the abundant yields.
T a b l e 5. Distribution of apples according to the diameter, %,
2002–2005
5
l e n t e l ë.
Obuoliø pasiskirstymas pagal skersmená, % 2002–2005 m.
Literature data show that yield of the different fruit tree branches significantly
Extra class. Fruit diameters 65 mm and more
Ekstra klasë. Vaisiø skersmuo – 65 mm ir daugiau
Orchard construction
Sodo konstrukcija
Spindle
Paprastoji verpstë,
average
2002
2003
2005
90.2
93.2
94.7
92.7
79.2
96.6
94.5
90.2
80.4
98.0
87.4
88.6
85.4
93.4
88.5
89.1
78.6
94.5
88.4
87.2
85.3
95.5
86.2
89.0
83.6
95.9
81.5
87.0
80.3
95.7
84.5
86.8
59.7
86.8
85.0
77.2
71.4
87.2
85.8
81.5
12.22
10.54
11.05
8.51
vidutiniškai
3x1m
Slender spindle
Laiboji verpstë, 3 x 1 m
Free growing leader
Laisvai augantis lyderinis vainikas,
3x1m
Super spindle
3 x 0.75 m
Slender spindle
Laiboji verpstë, 3 x 0.75 m
Super spindle
Superverpstë, 3 x 0.5 m
Super spindle, V system
Superverpstë, V forma, 3 x 0.5 m
Slender spindle
Laiboji verpstë, 3 x 0.5 m
Super spindle
Superverpstë, 3 x 0.25 m
Super spindle, V system
Superverpstë, V forma, 3 x 0.25 m
LSD05 / R05
Superverpstë,
depends on the position of the branch. If the branch is growing upward, the growth
prevails and yielding is being inhibited and vice versa – if the branch is horizontal or
hung down the yielding prevails and growth processes are being inhibited (Forshey
et al., 1992; Mika, 1998). Other investigators state that canopy forms do not influence
fruit tree yield (Krzewinska, Mika, 1998; Szewcuk, Sosna, 1998). Our investigations
showed that this process significantly depends on the growth vigour of the combination
139
of cultivar and rootstock. However, when growing the averagely vigorous cultivar
on super dwarf rootstock the growth is moderate and irrespective of the branch
growth – upward (free growing leader), horizontal (spindle), downward (slender
spindle) – all the branches grow moderately and yield abundantly. It is thought that
for the combinations of moderate vigorous cultivar and super dwarf rootstock this
is determined not by canopy form, but by the effect of the interaction of rootstock
and cultivar.
Fruit tree productivity, which includes fruit tree yield and growth vigour, showed
that in most cases averagely vigorous fruit trees on super dwarf rootstock P 22
planted at different distances and trained differently did not differ by their productivity.
Very densely planted fruit trees, which though yielded worse, but also grew much
more poorly, were significantly most productive ones. From the biological-economical
point of view, it is extremely important to obtain the abundant and high quality fruit
yields per unit of area. Makosz (1997) states that it is more economical to exploit the
orchards, which density is 2000–3000 trees / ha, than more sparse ones –
500–1200 trees / ha. Our investigations included even higher orchard density. The
results showed that super spindles trained in V system and planted at spacing of
3 x 0.25 m and super spindles trained in V system and planted at spacing of
3 x 0.25 m and 3 x 0.5 m were distinguished for the biggest average yield. The least
yield per unit of area was obtained in the most sparsely (3 x 1 m) planted variants. At
the same time it is necessary to evaluate that both the average fruit mass and fruit
size according to diameter of the most densely (3 x 0.25 m) grown fruit trees were
significantly smaller in comparison with fruits of the more sparsely grown fruit
trees.
The complex evaluation of the investigated apple tree cv. ‘Auksis’ on super
dwarf rootstock P 22 orchard constructions revealed the optimal orchard construction
for this combination of cultivar and rootstock – super spindles grown at spacing of
3 x 0.5 m. This orchard construction produces one of the best yields. Moreover, it
is very important that fruit average mass and size according to the diameter is
characteristic to this combination of cultivar-rootstock and do not get smaller as in
denser variants of the experiment.
Conclusions. 1. Apple tree cv. ‘Auksis’ on super dwarf rootstock P 22 start
abundant flowering already in the second year after planting. The abundance of fruit
tree flowering significantly depends neither on planting schemes, nor on crown forms.
2. Fruit tree yield in young age depend on planting schemes and almost doesn’t
depend on canopy form. Most sparsely (3 x 1 m) planted fruit trees produced the
biggest yield (3.98–4.57 kg/trees). The most densely (3 x 0.25 m) planted fruit trees
yielded significantly less of all (2.06–2.46 kg/trees).
3. According to the trunk diameter area the most vigorous are the most sparsely
(3 x 1 m and 3 x 0.75 m) planted fruit trees. The most densely (3 x 0.25 m) planted
fruit trees grew significantly less of all.
4. Significantly the most productive were the most densely (3 x 0.25 m) grown
fruit trees. Productivity of fruit trees on rootstock P 22 doesn’t depend on canopy
form and in most cases doesn’t depend on planting distance also when fruit trees are
planted at spacing 3 x 0.5 m and more sparsely.
140
5. Super spindles planted most densely in V system and super spindles planted
at spacings 3 x 0.25 m and 3 x 0.5 m were distinguished for the biggest average yield
per unit of area, correspondingly 32.82 t/ha and 26.14–27.54 t/ha. The smallest yield
per unit of area was obtained in most sparsely (3 x 1 m) planted variants (13.26–
15.22 t/ha).
6. Both the average fruit mass and fruit diameter of the most densely
(3 x 0.25 m) planted fruit trees were significantly smaller in comparison to the fruits
of more sparsely grown fruit trees. Fruit mass and fruit diameter in the orchards of
other constructions were almost the same.
7. After the complex evaluation of orchard constructions from the biologicaleconomical point of view we suggest to plant apple tree cv. ‘Auksis’ on super dwarf
rootstock P 22 at spacing of 3 x 0.5 m (6667 fruit trees / ha) and to train as super
spindles.
Acknowledgement. This work was partly supported by Lithuanian State Science
and Studies Foundation.
Gauta
2006 06 27
Parengta spausdinti
2006 07 26
References
1. C a l l e s e n O. Performance of ‘Discovery’ apple on M.9, M.26 and MM.106
rootstocks at two densities // J. Hort. Sci. 1995. V. 69(2). P. 305–313.
2. C h r o m e n k o V. V. Bases of productivity of cultivar, tree and plantation /
History, present and perspective of Russian horticulture. I.F. Kashin (eds.). Moscow,
2000. P. 279–290.
3. D e v i a t o v A. S. Productivity of apples on dwarf rootstocks at dense
planting system // Dwarf apple rootstocks in horticulture. 1997. P. 92–93.
4. F o r s h e y C. G., E l f o v i n g D. C., S t e b b i n s R. L. Training
and pruning apple and pear trees. Michigan, 1992. 160 p.
5. K r z e w i n s k a D., M i k a A. Effect of planting density and canopy form
on yield and fruit quality of cvs. ‘Jonagold’, ‘Gloster’ and ‘Idared’ // Proc. XXX VII
horticultural conference Skierniewice, 1998. P. 440–443.
6. L a k s o A. N., R o b i n s o n T. L. Principles of orchard systems
management optimizing supply, demand and partitioning in apple trees // Acta
Horticulturae. 1997. V. 451. P. 405–415.
7. L i c z n a r - M a l a n c z u k M. Wzrost I plonowanw dwoch odmian jabloni
przy rožnych systemach prowadzenia drzew w warunkach Dolnego Sl¹ska // Zesz. Nauk.
Ak. Roln. We Wroclawiu, 2001. Nr. 415. P. 51–71.
8. M a k o s z E. Economical evaluation of different apple planting schemes //
Strategy of fruit growing development in Poland until 2010. Lublin, 1997. P. 187–190.
9. M i k a A. Orchard models of XXI century // Proc. XXX VII horticultural
conference Skierniewice, 1998. P. 75–76.
141
10. M i k a A., K r a w e c A., B u l e r Z. et all. Wplyw systemow sadzienia,
formowania I ciêcia jabloni ‘Glister’ szczepionych na podkladkach skarlaj¹cych na
plonowanie intercepcjê igystrybucjê swiatla slonecznego w koronach drzew. // Zesz. Nauk.
Inst. Sad. I Kw. Skierniewicah, 2000. T. 8. P. 99–116.
11. S a d o w s k i A., B u c k o J., G u z e w s k i W. et all. Naswietlenie w
rožnych czêsciach korony I wybarwienie jablek ‘Jonagold’, w zaležnosci od zagêszczenia
drzew w sadzie // „Jakosc Owocow W Obliczu Globalizacji Producji Sadowniczej”. 2001. 74 p.
12. S a n s a v i n i S., B a s s i D., G i u n c h i L. Tree efficiency and fruit
quality in high-density apple orchards // Acta Hort. 1980. V. 114. P. 114–136.
13. S l o w i n s k i A., D z i u b a n R. Growth, cropping and fruit quality of
‘Gloster’ and ‘Elstar’ apple trees at two planting densities // Sodininkystë ir darþininkystë.
Babtai, 2002. V. 21(3). P. 113–117.
14. S z e w c u k A., S o s n a I. Development of model of intensive apple orchard
at Dalnego Slaska climatic conditions // Proc. Horticulture in Central and Eastern Europe.
Lublin, 1998. P. 213–220.
15. S z c z y g i e l A., K a d z i k F., M i k a A. Wplyw systemow I gênstosci
sadzienia na wzrost I owocowanie 4 odmian jabloni na pogorzu Karpackim. // Zesz. Nauk.
Inst. Sad. I Kw. Skierniewicah. 2000. T. 8. P. 87–97.
16. Ð a b a j e v i e n ë G., U s e l i s N., D u c h o v s k i s P. Investigation
of photosynthesis pigments of cultivar ‘Auksis’ in high density orchards of different
contruction. // Sodininkystë ir darþininkystë. Babtai, 2005. V. 24(4). P. 57–64.
17. U s e l i s N. Evolution of orchard constructions in Lithuania // Sodininkystë ir
darþininkystë Babtai, 2002. V. 21(3). P. 98–112.
18. U s e l i s N. Growth and productivity of dwarf apple trees in bearing orchards
of various constructions // Sodininkystë ir darþininkystë. Babtai, 2003. V. 22(1). P. 3–13.
19. W i d m e r A., K e r b s C. Influence of planting density and tree form on
yield and fruit quality of ‘Golden Delicious’ and ‘Royal Gala’ apples // Acta Horticulturae.
2001. V. 557. P. 235–241.
20. Y s t a a s J., H o v l a n d O., K v a l e A. Effect of tree density on
productivity and fruit quality of ‘Red Gravenstein’ on rootstocks M.9 and M.26 in singlerow system // Norwegian J. Agric. Sci. 1994. V. 8. P. 69–74.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
133–143.
SODINIMO SCHEMØ IR VAINIKO FORMØ ÁTAKA VAISMEDÞIØ SU P 22
POSKIEPIU PRODUKTYVUMUI IR VAISIØ KOKYBEI
N. Uselis, G. Ðabajevienë, P. Duchovskis
Santrauka
’Auksio‘ veislës obelø su P 22 poskiepiu sodinimo schemø ir vainiko formø bandymas
árengtas 2001 m. Lietuvos sodininkystës ir darþininkystës institute. Tyrimai atlikti jauname
sode 2002–2005 m. Tirti paprastosios verpstës formos vaismedþiai, pasodinti 3 x 1,5 m
atstumais, laibosios verpstës formos vaismedþiai, pasodinti 3 x 1 m ir 3 x 0,5 m, laisvai
auganèios lyderinës formos vaismedþiai, pasodinti 3 x 1 m, ir superverpstës formos
vaismedþiai, pasodinti 3 x 0,75 m, 3 x 0,5 m ir 3 x 0,25 m atstumais. Laibosios verpstës ir
142
superverpstës formos vaismedþiai dar tirti ir V formos konstrukcijos sode.
Nustatyta, kad ‘Auksio’ veislës obelys su labai þemu P 22 poskiepiu gausiai pradeda
þydëti jau antraisiais po sodinimo metais. Jaunø vaismedþiø derlingumas priklauso nuo
sodinimo schemø ir beveik nepriklauso nuo vainiko formos. Gausiausiai dera reèiausiai
(3 x 1 m) pasodinti vaismedþiai (3,98–4,57 kg/vaism.). Gausiausiu vidutiniu derlingumu ið
ploto vieneto iðsiskyrë tankiausiai V formos konstrukcijos sode pasodinti superverpstës
formos vaismedþiai (32,82 t/ha) ir tokios pat formos vaismedþiai, pasodinti 3 x 0,25 m ir
3 x 0,5 m atstumais (26,14–27,54 t/ha). Maþiausias derlius ið ploto vieneto gautas reèiausiai
(3 x 1 m) pasodintuose variantuose (13,26–15,22 t/ha). Tankiausiai (3 x 0,25 m) auginamø
vaismedþiø ir vidutinë vaisiaus masë, ir vaisiø skersmuo buvo ið esmës maþesni, palyginti
su reèiau auganèiø vaismedþiø vaisiais.
Kompleksiðkai biologiniu ir ûkiniu poþiûriu ávertinus tirtas sodo konstrukcijas,
vidutinio augumo ‘Auksio’ veislës vaismedþius su labai þemu P 22 poskiepiu siûloma
sodinti 3 x 0,5 m atstumais (6667 vaism./ha) ir formuoti superverpstës formos vainikus.
Reikðminiai þodþiai: augumas, derlingumas, obelys, sodinimo schemos, P 22,
produktyvumas, vainikø formos, vaisiø kokybë.
143
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 144–150.
COMPARISON OF 18 ROOTSTOCKS FOR APPLE TREE
CV. ‘ELISE’ IN V PLANTING SYSTEM
Dariusz WRONA, Andrzej SADOWSKI
Department of Pomology, Warsaw Agricultural University – SGGW,
Nowoursynowska 159, 02-787 Warszawa, Poland.
E-mail: [email protected]
The experiment was set up on a fertile alluvial soil, at the Warsaw-Wilanów
Experimental Station, Central Poland, in spring of 2000. Apple trees of cv. ‘Elise’ were
planted on 18 rootstocks of different origin and grew in V planting system. Different
rootstocks were classified into three groups, depending on expected tree vigour: semidwarfing (P 14, P 60, B.396 and M.26), dwarfing (B.9, B.146, P 2, P 59 and seven subclones
of M.9 – EMLA, Burgmer 984 & 751, T339, Pajam 1, Pajam 2, RN29) and superdwarfing
(M.27, P 16, PB-4). Trees on rootstocks assumed as semi-dwarfing were spaced at a
distance of 3.8 × 1.0 m, on dwarfing – at a distance of 3.5 × 0.7 m and on superdwarfing –
at a distance of 3.2 × 0.5 m. The trunk cross-sectional area (TCSA) after 6 years on semidwarfing rootstocks was the greatest on P 14; vigour of trees on other rootstocks was
similar. The cumulative yield per tree (2001–2005) was the lowest on M.26. Fruit size did
not depend on the rootstock. The cropping efficiency coefficient (CEC) was the highest
of trees on B.396 and the lowest – on P 14. On rootstocks considered as dwarfing, TCSA
after six years was the smallest on P 59 and the largest on M.9 EMLA; vigour of trees on
other subclones of M.9 was smaller and similar. The lowest cumulative yield per tree was
obtained on P 59 and the highest – on M.9 751, M.9 984 and M.9 EMLA. Fruit size was
similar and did not depend on rootstock. The CEC was the highest on P 59. On
superdwarfing rootstock trees on PB 4 were the smallest. The highest cumulative yield per
tree gave the trees on P 16, while on PB 4 – the lowest one. Fruit size did not depend on the
type of superdwarfing rootstock. In this group, CEC was the highest for trees on P 16.
Key words: apple, tree vigour, planting density, productivity, cumulative yield,
cropping efficiency, fruit size.
Introduction. For intensive planting system of apple fruit orchard, the ideal
tree is one that does not grow too vigorously, is early and regular bearing, and
produce high quality fruits (Wertheim, 1989; Vebster, 1992; Vercammen, 2004). M.9
EMLA is considered as standard and the most commonly used dwarfing rootstock
for high-density apple orchards. Its popularity is due to its moderate vigour, high
precocity of bearing, productivity of trees grown on it and good fruit size. Many
experiments with apple rootstocks have been carried out in different countries searching
144
for rootstocks best adapted to local climatic and soil conditions (Ferree et al., 1995;
Riesen and Monney, 1996; Quamme et al., 1999; Czynczyk et al., 2001; Sadowski et
al., 2004).
The aim of our experiment was to assess eighteen rootstocks of different origin
and vigour for cultivar ‘Elise’ planted in the “V” system.
Material and methods. The experiment was set up on a fertile salty loam
alluvial soil, at the Warsaw-Wilanów Experimental Station, Central Poland, in spring
of 2000. Apple trees ‘Elise’ on 18 rootstocks of different origin and vigour were
planted and trained in the V planting system. Different rootstocks were classified
into three groups, depending on expected tree vigour: semi-dwarfing (P 14, P 60,
B.396 and M.26), dwarfing (B.9, B.146, P 2, P 59 and seven subclones of M.9 –
EMLA, Burgmer 984 & 751, T339, Pajam 1, Pajam 2, RN29) and superdwarfing
(M.27, P 16, PB-4). Trees on rootstocks assumed as semi-dwarfing were spaced at
a distance of 3.8 × 1.0 m (2631 trees/ha), on dwarfing at a distance of 3.5 × 0.7 m
(4082 trees/ha) and on superdwarfing at a distance of 3.2 × 0.5 m (6250 trees/ha).
Each rootstock was represented by 10 trees per plot, in four replications. Alleyways
were under sward and herbicide strips were maintained along tree rows.
After six years, tree growth was estimated by the trunk cross-sectional area
(TCSA) derived from diameter measurements at 30 cm above the ground. The yield
was harvested every year and in this paper is presented as cumulative yield of five
years (2001–2005). Mean fruit mass was also determined. The cropping efficiency
coefficient (CEC) was calculated as a cumulative yield to the final TCSA ratio.
The results were elaborated by analysis of variance, separately for each group
of rootstocks. For evaluation of significance of differences between treatment means
the Newman-Keuls test was used, at α=0.05.
Results. After six years in the orchard (spring of 2006) the TCSA on semidwarfing rootstocks was the largest on P 14. The vigour of trees on other rootstocks
was similar (Table 1). The cumulative yield per tree (2001–2005) was the lowest on
M.26. Fruit size did not depend on the rootstock (Table 2). The cumulative cropping
efficiency coefficient (CEC) was the highest for trees on B.396 and the lowest on
P 14 (Table 5).
On rootstocks considered as dwarfing, TCSA after six years was the smallest
on P 59 and the largest on M.9 EMLA. No significant differences in vigour between
the different subclones of M.9 were noted (Table 1). The lowest cumulative yield
per tree was obtained on P 59 and the highest on M.9 751, M.9 984 and M.9 EMLA.
Fruit size was similar and did not depend on rootstock (Table 3). The CEC was the
highest on P 59 (Table 5).
On superdwarfing rootstocks the lowest TCSA had trees on PB 4, significantly
higher – on M.27 and the highest on P 16 (Table 1). The highest cumulative yield per
tree gave the trees on P 16, while on PB 4 – the lowest. Fruit size did not depend on
the type of superdwarfing rootstock (Table 4). In this group, CEC was the highest
for trees on P 16 (Table 5).
145
T a b l e 1. Size of apple tree cv. ‘Elise’ six years after planting
(spring of 2006)
1
l e n t e l ë.
‘Elise’ veislës obelø dydis, praëjus ðeðeriems metams po pasodinimo,
2006 m. pavasaris
Trunk crossSemidwarfing sectional area
rootstock
(TCSA)
Pusiau
þemaûgiai
poskiepiai
Kamieno
skerspjûvio
plotas (KSP),
Dwarfing
rootstock
Þemaûgiai
poskiepiai
Trunk crosssectional area Superdwarfing
(TCSA)
rootstock
Kamieno
skerspjûvio
plotas (KSP),
cm2
P 14
P 60
B.396
M.26
36.0 b
20.16 a
18.60 a
22.15 a
Trunk crosssectional area
(TCSA)
Nykštukiniai
poskiepiai
Kamieno
skerspjûvio
plotas (KSP),
cm2
18.83 d
16.93 cd
16.68 cd
14.79 bc
14.74 bc
17.74 cd
14.66 bc
4.40 bc
12.11 b
15.95 cd
7.23 a
M.9 EMLA
M.9 984
M.9 751
M.9 T339
M.9 Pajam 1
M.9 Pajam 2
M.9 RN29
B.9
B.146
P2
P 59
cm2
M.27
P 16
PB 4
7.65 b
8.20 b
5.69 a
T a b l e 2. The cumulative yield (2001–2005) and mean fruit mass of
apple tree cv. ‘Elise’ on semi-dwarfing rootstocks
2
l e n t e l ë.
‘Elise’ veislës obelø su pusiau þemaûgiais poskiepiais suminis
derlius (2001–2005 m.) ir vidutinë vaisiaus masë
Rootstock
Yield (kg tree-1)
Mean fruit mass
Poskiepis
Derlius, kg medis-1
Vidutinë vaisiaus masë, g
P 14
P 60
B.396
M.26
49.9 b
50.3 b
56.8 b
42.1 a
220 a
225 a
233 a
222 a
T a b l e 3. The cumulative yield (2001–2005) and mean fruit mass of
apple tree cv. ‘Elise’ on dwarfing rootstocks
3
l e n t e l ë.
‘Elise’ veislës obelø su þemaûgiais poskiepiais suminis derlius
(2001–2005 m.) ir vidutinë vaisiaus masë
Rootstock
Yield (kg tree-1)
Mean fruit mass
Poskiepis
Derlius, kg medis-1
Vidutinë vaisiaus masë, g
M.9 EMLA
M.9 984
M.9 751
M.9 T339
M.9 Pajam 1
M.9 Pajam 2
M.9 RN29
B.9
B.146
P2
P 59
231 a
230 a
239 a
230 a
237 a
240 a
231 a
226 a
230 a
230 a
217 a
49.3 b
48.5 b
50.1 b
43.7 ab
46.9 ab
46.0 ab
39.2 ab
43.2 ab
38.9 ab
37.4 ab
31.3 a
146
T a b l e 4. The cumulative yield (2001–2005) and mean fruit mass of
apple tree cv. ‘Elise’ on superdwarfing rootstocks
4
l e n t e l ë. ‘Elise’ veislës obelø su nykðtukiniais poskiepiais suminis derlius
(2001–2005 m.) ir vidutinë vaisiaus masë
Rootstock
Yield (kg tree-1)
Poskiepis
Derlius, kg medis-1
M.27
P 16
PB 4
Mean fruit mass
Vidutinë vaisiaus masë,
21.9 b
29.5 c
16.6 a
g
166 a
176 a
162 a
T a b l e 5. Cropping efficiency coefficient of apple tree cv. ‘Elise’
5
l e n t e l ë. ‘Elise’ veislës obelø produktyvumas
Semidwarfing
CEC
rootstock
Produktyvumas,
Pusiau þemaûgiai
kg cm-2
poskiepiai
P 14
P 60
B.396
M.26
1.39 a
2.51 b
3.12 c
1.90 a
Dwarfing
rootstock
Þemaûgiai
poskiepiai
Superdwarfing
CEC
CEC
rootstock
Produktyvumas,
Produktyvumas,
Nykštukiniai
kg cm-2
kg cm-2
poskiepiai
2.63 a
2.88 a
3.00 a
3.03 a
3.22 a
2.64 a
2.66 a
3.02 a
3.19 a
2.36 a
4.34 b
M.9 EMLA
M.9 984
M.9 751
M.9 T339
M.9 Pajam 1
M.9 Pajam 2
M.9 RN29
B.9
B.146
P2
P 59
M.27
P 16
PB 4
2.88 a
3.65 b
2.93 a
Discussion. Kurlus and Ugolik (1996), Sadowski et al. (1997) and Wlosek and
Jadczuk (1998) reported that trees on P 14 showed the highest vigour; branches of
trees spaced at 1 m in the row overlapped, and this indicated that this rootstock was
too vigorous in comparison with other rootstocks classified as semi-dwarfing and
dwarfing. Czynczyk et al. (2001) confirmed their opinion that trees on P 14 grew
too vigorously in the first years only. Later the growth of trees on P 14 is usually
much weaker. Results of above-mentioned authors partly confirmed our experiment.
The growth of trees on P 14 was stronger than M.26 and other rootstock, both at
the first years after planting and after six years. Fruit bud formation on P 14 was
delayed, and CEC was the lowest. Similar results were also obtained by Skrzyñski
and Poniedziaùek (2000) and Sùowiñski (2004).
In the present study none of the M.9 subclone had any consistent effect on the
trunk diameter of trees and yield in the orchard, however trees on M.9 EMLA showed
a slightly more vigorous growth and better yielding. Our report corresponded to the
results obtained by Loreti et al. (2001) and Webster et al. (2000), who pointed that
size of trees on M.9 subclones was similar; albeit some differences in vigour of trees
and yielding on some subclones and on M.9 EMLA had been noticed. Czynczyk et al.
(2001) pointed that trees on P 59 grew weakly, and yielded not very abundantly,
147
what is in line with our study. Trees on P 59 were the smallest and gave the low
yield.
According to Ùukuã (1994), trees on rootstock PB 4 have similar vigour to
M.9. Our experiment did not confirm this opinion. Tress on PB 4 were very dwarfing,
showing in the orchards weaker vigour than M.27 and P 16. This confirms the
observations of Sadowski et al. (2000, 2004), who described its vigour as lower
than on M.9 and even on P 22. Dwarfing effect of PB 4 as well P 22 has been
successively intensified; the contrast between trees on PB 4 and M.9 increased with
the age.
Conclusions. 1. Trees on semi dwarfing rootstock P 14 showed too vigorous
growth, delayed fruit bud formation and had the lower cropping efficiency coefficient.
On fertile soils in particular this rootstock is not acceptable for high-density plantings.
2. Dwarfing rootstock M.9 EMLA and other subclones of M.9 providing early
bearing and high productivity but not significant differences in vigour and yielding
between them were noted. This rootstock remains as universal rootstock for intensive
orchard.
3. For intensive orchard the most promising alternative rootstock for M.9 is
P 16. Trees on this rootstock had a relatively low vigour and high cropping efficiency
coefficient.
Gauta
2006 05 12
Parengta spausdinti
2006 07 13
References
1. C z y n c z y k A., B i e l e c k i P., B a r t o s i e w i c z B. Testing new
dwarfing apple rootstocks from Polish and foreign breeding programmes. Acta Hort. 2001.
557. P. 83-89.
2. F e r r e e D. C., H i r s t P. M., S c h m i d J. C., D o t s o n P. E.
Performance of three apple cultivars with 22 dwarfing rootstocks during 8 seasons in
Ohio. Fruit Var. 1995. J. 49(3). P. 171-178.
3. K u r l u s R., U g o l i k M. Wzrost i plonowanie drzew jabùoni Szampion,
Rogal Gala i Jonagored na podkùadkach polskiej hodowli. XXXIV Ogólnopolska Konf.
Sad. 1996. P. 271-273.
4. L o r e t i F., M a s s a i R., F e i C., C i n e l l i F. C e c c o n i B.
Evaluation of eleven dwarfing apple rootstock: preliminary results. Acta Hort. 2001. 557.
P. 155-161.
5. Ù u k u ã T. PB 4 – obiecujàca podkùadka dla jabùoni. Sad Nowoczesny. 1994. (7).
9 p.
6. Q u a m m e H. A., H a m p s o n C. R., B r o w n l e e R. T. Apple
rootstock evaluation for the climate of British Columbia. Proc. Int. Seminar „Apple
Rootstocks for Intensive Orchards” (Warsaw-Ursynów, Poland, 18–21.08.1999). 1999.
P. 87-88.
7. R i e s e n W., M o n n e y P. Apfelunterlagen: Zwischenergebnisse deutsch
und westschweizerischer Versuche. Obst und Weinbau. 1996. 132(21). P. 548-552.
148
8. S a d o w s k i A., M a c i e j c z a k G., W r o n a D. Growth and early
bearing of ‘Ðampion’apple trees depending on rootstock and tree quality. Internat. Conf.
„Modern Orchards: Achievements and Tendencies”. Collection of Scientific Articles. 1997.
P. 28-34.
9. S a d o w s k i A., G r o c h o w a l s k i W., S ù o w i ñ s k i A.,
Ý ó ù t o w s k i J. Ocena siùy wzrostu jabùoni na podkùadce PB 4. Zesz. Nauk. Ins. Sad.
I Kw. Skierniewice. 2000. 8. P. 71-76.
10. S a d o w s k i A., D z i u b a n R., J a b ù o ñ s k i K. Growth and
cropping of three apple cultivars on different rootstocks over a 7-year period. Acta Hort.
2004. 658. P. 257-263.
11. S k r z y ñ s k i J., P o n i e d z i a ù e k W. Wzrost i plonowanie odmiany
‘Jonagold’ na kilku podk³adkach wegetatywnych. Zesz. Nauk. Inst. Sad. I Kwiat. W
Skierniewicach. 2000. T. 8. P. 53-58.
12. S ù o w i ñ s k i A. Comparison of 22 rootstock of different vigour and origin
used for Elise apple trees. Acta Hort. 2004. 658. P. 279-286.
13. W e r t h e i m S. J. Preliminary results of trials with dwarfing apple and pear
rootstock. Acta Hort. 1989. 243. P. 59-70.
14. W e b s t e r A. D. New dwarfing rootstocks for apple, pear, plum and sweet
cherry – a brief review. Acta Hort. 1992. 349. P. 145-153.
15. W e b s t e r T., T o b u t t K., E v a n s K. Breeding and evaluation of
new rootstocks for apple, pear and sweet cherry. Compact Fruit Tree. 2000. 33(4). P. 100-104.
16. W l o s e k S t a n g r e d C. R., J a d c z u k E. Wpùyw podkùadki na
wzrost i plonowanie jab³oni. XXXVII Ogólnopolska Konf. Sad. 1998. P. 526-527.
17. Vercammen J. Search for a more dwarfing rootstock for apple. Acta Hort. 2004.
658. P. 313-318.
149
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
144–150.
‘ELISE’ OBELØ VEISLËS SU 18 POSKIEPIØ PALYGINIMAS V FORMOS
SODINIMO SISTEMOJE
D. Wrona, A. Sadowski
Santrauka
Bandymas pradëtas derlingoje aliuvinëje dirvoje Varðuvos-Vilanovo eksperimentinëje
stotyje, Centrinëje Lenkijoje, 2000 metø pavasará. ‘Elise’ veislës obelys buvo pasodintos
su 18 skirtingos kilmës poskiepiø ir augo V formos sodinimo sistemoje. Skirtingi poskiepiai
buvo suskirstyti á tris grupes, priklausomai nuo vaismedþio tikëtino augumo: pusiau
þemaûgiai (P 14, P 60, B.396 ir M.26), þemaûgiai (B.9, B.146, P 2, P 59 ir septyni M.9
subklonai – EMLA, Burgmer 984 ir 751, T339, Pajam 1, Pajam 2, RN29) ir nykðtukiniai
(M.27, P 16, PB-4). Vaismedþiai su pusiau þemaûgiams priskirtais poskiepiais buvo pasodinti
3,8 × 1,0 m, su þemaûgiais – 3,5 × 0,7 m ir su nykðtukiniais – 3,2 × 0,5 m atstumais. Po 6 metø
pusiau þemaûgiø poskiepiø grupëje didþiausias buvo kamieno skerspjûvio plotas (KSP)
vaismedþiø su P 14 poskiepiu; vaismedþiø augumas su kitais poskiepiais buvo panaðus.
2001–2005 m. maþiausias suminis derlius buvo vaismedþio su M.26 poskiepiu. Vaisiø dydis
nuo poskiepiø nepriklausë. Produktyviausi buvo vaismedþiai su B.396, o maþiausiai
produktyvûs – su P 14 poskiepiu. Ið þemaûgiams priskirtø poskiepiø grupës po ðeðeriø
metø maþiausias KSP buvo vaismedþiø su P 59, didþiausias – su M.9 EMLA poskiepiu.
Vaismedþiø augumas su kitais M.9 subklonais buvo maþesnis, bet panaðus. Maþiausias
suminis derlius buvo vaismedþio su P 59, didþiausias – su M.9 751, M.9 984 ir M.9 EMLA
poskiepiais. Vaisiø dydis buvo panaðus ir nuo poskiepiø nepriklausë. Produktyviausi
vaismedþiai buvo su P 59 poskiepiu. Ið nykðtukiniø poskiepiø augumà labiausiai sumaþino
PB-4. Didþiausias suminis derlius buvo vaismedþiø su P 16, maþiausias – su PB-4 poskiepiu.
Vaisiø dydis nuo nykðtukiniø poskiepiø rûðies nepriklausë. Ðioje grupëje produktyviausi
buvo vaismedþiai su P 16 poskiepiu.
Reikðminiai þodþiai: obelys, vaismedþiø augumas, sodinimo tankumas, derlingumas,
suminis derlius, produktyvumas, vaisiø dydis.
150
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 151–157.
INFLUENCE OF ROOTSTOCKS AND PLANTING
SCHEMES OF APPLE TREE CV. ‘LIGOL’ ON
PRODUCTIVITY AND FRUIT QUALITY
Nobertas USELIS
Lithuanian Institute of Horticulture, LT-54333, Babtai, Kaunas distr.,
Lithuania.E-mail: [email protected]
The experiment of apple tree cv. ‘Ligol’ rootstocks and planting schemes was arranged
at the Lithuanian Institute of Horticulture in 1999. Investigations were carried out in
young orchard in 2001–2005. There were investigated fruit trees of cv. ‘Ligol’ on rootstock
P 60 planted at spacing of 4 x 2 m (1250 trees / ha), on rootstock P 2 planted at spacings of
4 x 2 m (1250 trees/ha) and 4 x 1.5 m (1667 trees/ha), and on rootstock P 22 planted at
spacings of 4 x 1.5 m (1667 trees/ha) and 4 x 1 m (2500 trees/ha). It was established that
apple tree cv. ‘Ligol’ on rootstock P 2 and P 60 yielded most abundantly (21.1–
22.9 kg / tree). Apple trees on super dwarf rootstock P 22 yields significantly loss (9.2–
11.0 kg / tree). Fruit trees of cv. ‘Ligol’ on rootstock P 60 and P 2 were the most vigorous,
and these on rootstock P 22 – the most productive ones. Significantly the biggest average
fruit yield per unit of area was obtained from fruit trees of cv. ‘Ligol’ on rootstocks P 60 and
P 2 (26.4–28.6 t/ha). When the distances among fruit trees on rootstocks P 2 and P 22 were
decreased by 0.5 m, the yield increased insignificantly. Fruit trees on more vigorous
rootstocks P 60 and P 2 produce significantly the biggest fruits and their mass does not
depend on planting distances. From the practical point of view it is suggested to grow in
commercial orchards fruit trees of cv. ‘Ligol’ on rootstocks P 2 and P 60 spaced at
4 x 1.5–2 m.
Key words: growth vigour, apple trees, rootstocks, productivity, planting schemes,
fruit quality.
Introduction. When planting commercial orchards it is very important to choose
the proper combinations of apple tree cultivars and rootstocks in order orchards
would start early yielding and would produce the abundant and high quality fruit
yields. One of the most reliable and most widely applied means in commercial fruit
growing to attain more early fruit tree yielding and to increase the productivity is the
use of dwarf rootstocks. The investigations of dwarf rootstocks in the orchard
were carried out in various agroclimatic zones and a lot of data was collected (Bite,
Lepsis, 2004; Slowinski, 2004 ). There were conducted many investigations at the
Lithuanian Institute of Horticulture both in nursery and orchard (Kviklys et al., 1999;
Kviklys et al., 2000; Kviklys, 2002). Nevertheless, it is necessary to find the optimal
151
combinations of cultivar and rootstock and also the corresponding planting schemes
for apple trees of every more important cultivar taking into account agroclimatic and
economical conditions of the country (Maas, Werthem, 2004).
T h e a i m o f t h e i n v e s t i g a t i o n was to evaluate the influence
of dwarf rootstocks and planting schemes on the productivity and fruit quality of
one of the most important winter apple tree cv. ‘Ligol’ in the young age.
Material and methods. The experiment of apple tree cv. ‘Ligol’ rootstocks
and planting schemes was arranged at the Lithuanian Institute of Horticulture in
1999. Investigations were carried out in young orchard in 2001–2005.
The scheme of the experiment: 1) fruit trees on rootstock P 60, planting scheme
4 x 2 m (1250 trees/ha); 2) fruit trees on rootstock P 2, planting scheme 4 x 2 m
(1250 trees/ha); 3) fruit trees on rootstock P 2, planting scheme 4 x 1.5 m
(1667 trees/ha); 4) fruit trees on rootstock P 22, planting scheme 4 x 1.5 m
(1667 trees/ha); 5) fruit trees on rootstock P 22, planting scheme 4 x 1 m
(2500 trees/ha).
The investigation consisted of 4 replications with 5 fruit trees in each
experimental plot, 3 of them were accounting. There was evaluated: fruit tree flowering
abundance in scores, where 0 – fruit trees do not flower at all and 5 – fruit trees
flower very abundantly; trunk diameter (cm2) – at the height of 0.25 m, yield
(kg/fruit tree and t/ha), fruit tree productivity (kg/cm2), the average fruit mass (g).
The data of investigation were evaluated by ANOVA.
The changes of meteorological conditions during investigations didn’t influence
significantly the means, which were being analyzed, with the exception of 2004
when strong frosts in May destroyed two thirds of apple tree blossoms.
Experimental orchard was maintained on the technologies of the intensive
commercial orchards (Uselis, 2005). Fruit trees were trained as slender spindles.
Results. The experimental apple trees flowered very abundantly in 2001, 2003
and 2005. In 2002 and 2004 apple tree flowered less. The average apple tree flowering
during five years reached 3.98–4.13 scores and significantly didn’t depend on
rootstock (Table 1).
The average fruit yield of apple trees cv. ‘Ligol’ strongly depended on rootstock.
According to five-year data, apple trees on rootstock P 60 yielded most abundantly
(Table 1). The similar yield was obtained from apple trees on rootstock P 2. Meanwhile
apple trees on rootstock P 22 yielded significantly less. It was observed the tendency
that apple trees on the same rootstocks but planted more densely yielded less, even
though statistically significant differences weren’t obtained (Table 1).
Fruit tree growth vigour according to the trunk cross-section area strongly
depended on the rootstock they were grown. It was established that fruit trees on
rootstocks P 60 and P 2 didn’t differ according to the trunk cross-section area
(Table 2). Meanwhile the trunk cross-section area of fruit trees on rootstock P 22
was significantly smaller than that of fruit trees on rootstocks P 60 or P 2.
It was established that fruit trees on super dwarf rootstock P 22 were the most
productive ones (Table 2). Fruit trees on more vigorous rootstocks P 60 and P 2
were significantly less productive. Fruit tree planting distances investigated in the
experiment didn’t influence significantly their productivity.
152
T a b l e 1. The influence of rootstocks on flowering abundance and
yield of apple tree cv. ‘Ligol’, 2001–2005
1
l e n t e l ë.
Poskiepiø átaka ‘Ligol’ veislës obelø þydëjimo gausumui ir derliui
2001–2005 m.
Rootstock, planting scheme
Flowering abundance, 0-5 scores
Yield, kg / tree
Poskiepis, sodinimo schema
Þydëjimo gausumas balais
Derlius, kg/vaism.
4.01
22.9
4.12
21.1
4.21
17.7
3.98
11.0
4.13
9.2
0.69
6.23
P 60, 4 x 2 m, 1250 trees/ha
P 60, 4 x 2 m, 1250 vaism./ha
P 2, 4 x 2 m, 1250 trees/ha
P 2, 4 x 2 m, 1250 vaism./ha
P 2, 4 x 1.5 m, 1667 trees/ha
P 2, 4 x 1.5 m, 1667 vaism./ha
P 22, 4 x 1.5 m, 1667 trees/ha
P 22, 4 x 1,5 m, 1667 vaism./ha
P 22, 4 x 1 m, 2500 trees/ha
P 22, 4 x 1 m, 2500 vaism./ha
LSD05 / R05
T a b l e 2. The influence of rootstocks on growth vigour and
productivity of apple tree cv. ‘Ligol’, 2001–2005
2
l e n t e l ë.
Poskiepiø átaka ‘Ligol’ veislës obelø augumui ir produktyvumui
2001–2005 m.
Rootstock, planting scheme
Poskiepis, sodinimo schema
P 60, 4 x 2 m, 1250 trees / ha
Trunk cross-section area
(TCSA) / Kamienëlio skerspjûvio
Productivity 2001–2005,
kg/cm2 TCSA / Produktyvumas
plotas (KSP) 2005 m., cm2
2001–2005 m., kg/cm2 KSP
37.3
3.07
34.6
3.05
36.7
2.41
12.9
4.26
10.6
4.34
11.55
1.102
P 60, 4 x 2 m, 1250 vaism./ha
P 2, 4 x 2 m, 1250 trees / ha
P 2, 4 x 2 m, 1250 vaism./ha
P 2, 4 x 1.5 m, 1667 trees / ha
P 2, 4 x 1,5 m, 1667 vaism./ha
P 22, 4 x 1.5 m, 1667 trees / ha
P 22, 4 x 1,5 m, 1667 vaism./ha
P 22, 4 x 1 m, 2500 trees / ha
P 22, 4 x 1 m, 2500 vaism./ha
LSD05 / R05
One of the most important indices is fruit yield per unit of area. The first abundant
fruit yield per unit of area was obtained in 2001. This yield didn’t depend on fruit tree
rootstock. More densely (4 x 1.5 m) planted fruit trees on rootstock P 2 yielded
significantly more abundantly than these, which were planted more sparsely
(4 x 2 m) (Table 3). The same tendency was observed with the rootstock P 22. More
densely (4 x 1 m) planted fruit trees on rootstock P 22 yielded more abundantly than
these, which were planted more sparsely (4 x 1.5 m).
153
T a b l e 3. The influence of rootstocks on yield of apple tree
cv. ‘Ligol’, t/ha, 2001–2005
3
l e n t e l ë. Poskiepiø átaka ‘Ligol’ veislës obelø derliui, t/ha 2001–2005 m.
Rootstock, planting scheme
Poskiepis, sodinimo schema
P 60, 4 x 2 m, 1250 trees/ha
2001
2002
2003
2004
2005
22.5
12.2
54.2
6.2
47.9
23.1
11.1
45.8
7.1
44.9
34.8
13.5
52.8
10.7
35.5
22.5
10.8
30.8
14.8
12.5
27.0
14.7
31.0
20.0
22.0
10.20
5.01
12.52
6.25
13.02
P 60, 4 x 2 m, 1250 vaism./ha
P 2, 4 x 2 m, 1250 trees/ha
P 2, 4 x 2 m, 1250 vaism./ha
P 2, 4 x 1.5 m, 1667 trees/ha
P 2, 4 x 1,5 m, 1667 vaism./ha
P 22, 4 x 1.5 m, 1667 trees/ha
P 22, 4 x 1,5 m, 1667 vaism./ha
P 22, 4 x 1 m, 2500 trees/ha
P 22, 4 x 1 m, 2500 vaism./ha
LSD05 / R05
After the productive first year fruit trees yielded worse and the second yield
was twice as smaller. There weren’t significant differences among fruit trees on
different rootstocks; only it was observed the tendency that more densely planted
fruit trees on the same rootstocks produced more abundant yields per area (Table 3).
In 2003 the experimental orchard yielded very abundantly. The biggest yield was
obtained from fruit trees on rootstock P 60, also the similar yields were obtained
from fruit trees on rootstock P 2. Meanwhile fruit trees on super dwarf rootstock
P 22 produced statistically significantly smaller yield per unit of area. The similar
results were obtained in 2005. In 2004 after strong frosts the yield very varied, but
the most densely grown fruit trees on super dwarf rootstock P 22 yielded best of all.
The biggest average fruit yield per unit of area during the five years of investigation
was obtained from fruit trees ‘Ligol’ on rootstocks P 2 and P 60 spaced at 4 x 2 m
– respectively 26.4 t/ha and 28.6 t/ha (Table 4). When growing fruit trees on super
dwarf rootstock P 22, even though planted more densely, there was obtained the
smallest yield per unit of area (18.3 t/ha). When the distances among fruit trees on
both rootstocks P 2 and P 22 were reduced by 0.5 m, the yield increased, but there
weren’t significant differences.
Fruit trees on more vigorous rootstocks P 60 and P 2 produced the biggest
fruits. Their mass independently on planting distance was 200–209 g. Fruit trees on
superdwarf rootstock P 22 produced significantly smaller fruits (Table 4).
Discussion. When choosing the rational construction of the commercial orchard
it is very important to choose the optimal combinations of cultivar and rootstock, the
corresponding fruit tree canopy forms and planting schemes. It is indicated in the
literature (Kviklys et al., 1999; Uselis, 2005) that fruit trees on rootstocks P 60 and
P 2 are more vigorous therefore they are planted more sparsely, and fruit trees on
rootstock P 22 are less vigorous, therefore they are planted more densely. The
tendencies of fruit tree vigour were confirmed by the data of this experiment also,
when trunk cross-section area of fruit trees on rootstocks P 60 and P 2 was more
than three times bigger in comparison to that of fruit trees on rootstock P 22. The
154
analogical data are being obtained of fruit tree yield also. It was established in the
investigation that the more vigorous dwarf fruit trees are (on more vigorous rootstocks
P 60 and P 2), more abundantly they yield in comparison with these fruit trees on
rootstock P 22, which growth vigour is very weak. The similar data, that the smaller
rootstock, the poorer yielding of fruit tree, were obtained by other authors too (Barritt
et al., 2004). Nevertheless, there are data in the literature that yield of apple tree cv.
‘Ligol’ on these rootstocks significantly do not differ (Czynczyk et al., 2004).
T a b l e 4. The influence of rootstocks on the average fruit yield
(t/ha) and fruit mass (g) of apple tree cv. ‘Ligol’, 2001–
20054
4
l e n t e l ë. Poskiepiø átaka ‘Ligol’ veislës obelø vidutiniam vaisiø derliui (t/ha)
ir vaisiø masei (g) 2001–2005 m.
Rootstock, planting scheme
Average yield
Poskiepis, sodinimo schema
Vidutinis derlius, t/ha
Vidutinë vaisiaus masë, g
28.6
209
26.4
200
29.5
200
18.3
156
23.0
148
7.11
37.2
P 60, 4 x 2 m, 1250 trees/ha
Average fruit mass
P 60, 4 x 2 m, 1250 vaism./ha
P 2, 4 x 2 m, 1250 trees/ha
P 2, 4 x 2 m, 1250 vaism./ha
P 2, 4 x 1.5 m, 1667 trees/ha
P 2, 4 x 1,5 m, 1667 vaism./ha
P 22, 4 x 1.5 m, 1667 trees/ha
P 22, 4 x 1,5 m, 1667 vaism./ha
P 22, 4 x 1 m, 2500 trees/ha
P 22, 4 x 1 m, 2500 vaism./ha
LSD05 / R05
Fruit tree productivity is the complex index, which include fruit tree growth
vigour and fruit tree yield. It showed that fruit trees of the weakest vigour on rootstock
P 22 are significantly the most productive ones. Nevertheless, in commercial
horticulture there isn’t enough of this index only and it is much more important the
yield per unit of area and fruit quality. There was established in the investigation that
fruit trees on rootstock P 22, despite the biggest productivity per unit of area, produced
significantly the smallest yield. Even fruit tree densifying in the rows didn’t change
productivity significantly.
The second very important index is fruit quality. There was established in the
investigation that fruit trees on rootstock P 22 produced significantly smaller fruits,
even though there are data in the literature that the mass of fruits of fruit trees on
rootstocks P 60 and P 22 is similar (Czynczyk et al., 2004).
In most cases the tendency was observed that the further fruit tree densifying
in the rows decreases fruit tree yield, but the yield per unit of area slightly increases.
This is confirmed densifying by abundant data of the other authors also (Deviatov,
1997; Mika, 1998; Uselis, 2003).
After the complex evaluation of fruit trees ‘Ligol’ on rootstocks P 60, P 2 and
P 22 planted at different spacing, it is possible to state that from the practical point of
view it is best of all to grow in commercial orchards fruit trees of cv. ‘Ligol’ on
155
rootstocks P 2 and P 60 planted at spacing of 4x1.5 m. It is advisable not to grow
apple trees of cv. ‘Ligol’ on rootstocks P 22 or to grow them only if they are being
irrigate, because of their poorer yield and especially worse fruit quality. Investigations
by Petronis (2002) showed that when irrigating ‘Ligol’ on rootstock P 22 fruit yield
significantly increases and fruit quality improves.
Conclusions. 1. The average fruit tree flowering abundance does not depend
on rootstock. According to the average data, apple trees of cv. ‘Ligol’ on rootstocks
P 2 and P 60 produce the biggest yield (21.1–22.9 kg/tree). Apple trees on super
dwarf rootstock P 22 yield significantly less (9.2–11.0 kg/trees).
2. Most vigorous fruit trees are on rootstocks P 60 and P 2, most productive
ones – on rootstock P 22.
3. The biggest fruit yield per unit of area was obtained from apple trees of
cv. ‘Ligol’ on rootstocks P 2 and P 60 spaced at 4 x 2 m – respectively 26.4 t/ha and
28.6t/ha. When the distances among fruit trees on rootstocks P 2 and P 22 were
decreased by 0.5 m, the yield increased insignificantly.
4. Fruit trees on more vigorous rootstocks P 60 and P 2 produce the biggest
fruits and their mass does not depend on planting distances.
5. From the practical point of view it is best of all to grow in commercial
orchards apple trees of cv. ‘Ligol’ on rootstocks P 2 and P 60 planted at spacing of
4 x 1.5-2 m.
Acknowledgement. This work was partly supported by Lithuanian State Science
and Studies Foundation.
Gauta
2006 07 01
Parengta spausdinti
2006 07 27
References
1. B a r r i t t B. H., K o n i s h i B. S. and D i l l e y M. A. The influence
of 12 M.9 clones and 12 other dwarfing rootstocks on ‘Fuji’ apple tree growth, productivity
and susceptibility to Southwest trunk injury in Washington // Acta Horticulturae. Zaragosa,
2004. N. 658. V. 1. P. 103–109.
2. B i t e A. and L e p s i s J. The results of extended duration testing of apple
rootstocks in Latvia // Acta Horticulturae. Zaragosa, 2004. N. 658. V. 1. P. 115–118.
3. D e v i a t o v A. S. Productivity of apples on dwarf rootstocks at dense planting
system // Dwarf apple rootstocks in horticulture. 1997. P. 92–93.
4. C z y n c z y k A., B i e l i c k i P., B a r t o s i e w i c z B. Influence of
subclones of M.9 and P 22 and new polish-bred rootstocks on growth and yields of
‘Jonagold’ and ‘Ligol’ apple trees // Acta Horticulturae. Zaragosa, 2004. N. 658. V. 1.
P. 129–133.
5. K v i k l y s D., U s e l i s N., K v i k l i e n ë N. Rootstock effect on
‘Jonagold’ apple tree growth, yield and fruit quality // Apple rootstocks for intensive
orchards. Warszawa, 1999. P. 67–69.
156
6. K v i k l y s D., P e t r o n i s P., K v i k l i e n ë N. Effects of apple
rootstocks on the yield and fruit quality // Sodininkystë ir darþininkystë. Babtai, 2000.
V. 19(1). P. 23–31.
7. K v i k l y s D. Apple rootstock research in Lithuania with aspect to fruit quality
and tree productivity // Sodininkystë ir darþininkystë. Babtai, 2002. V. 21(3). P. 3–13.
8. M a a s F. M., W e r t h e i m S. J. A multi-site rootstock trial with the
apple cultivars ‘Cox’s Orange Pippin’ and ‘Jonagold’ // Acta Horticulturae. Zaragosa,
2004. N. 658. V. 1. P. 177–184.
9. M i k a A. Orchard models of XXI century // Proc. XXXVII horticultural conference
Skierniewice, 1998. P. 75–76.
10. P e t r o n i s P. Efficiency of irrigation fir young dwarf ‘Ligol’ apple trees //
Sodininkystë ir darþininkystë. Babtai, 2002. V. 21(4). P. 39–44.
11. S l o w i n s k i A. Comparison of 22 rootstocks of different vigour and origin
used for ‘Elise’ apple trees // Acta Horticulturae. Zaragosa, 2004. N. 658. V. 1. P. 279–286.
12. U s e l i s N. Growth and productivity of dwarf apple trees in bearing orchards
of various constructions // Sodininkystë ir darþininkystë. Babtai, 2003. V. 22(1). P. 3–13.
13. U s e l i s N. Intensyvios obelø ir kriauðiø auginimo technologijos. Babtai,
2005. 210 p.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
151–157.
POSKIEPIØ IR SODINIMO SCHEMØ ÁTAKA ‘LIGOL’ VEISLËS OBELØ
PRODUKTYVUMUI IR VAISIØ KOKYBEI
N. Uselis
Santrauka
‘Ligol’ veislës obelø poskiepiø ir sodinimo schemø bandymai árengti 1999 m. Lietuvos
sodininkystës ir darþininkystës institute. Tyrimai atlikti jauname sode 2001–2005 m. Tirti
‘Ligol’ veislës vaismedþiai su P 60 poskiepiu, pasodinti 4 x 2 m atstumais (1250 vaism./ha),
su P 2 poskiepiu, pasodinti 4 x 2 m (1250 vaism./ha) ir 4 x 1,5 m atstumais (1667 vaism./ha),
ir su P 22 poskiepiu, pasodinti 4 x 1,5 m (1667 vaism./ha) ir 4 x 1 m atstumais
(2500 vaism./ha). Nustatyta, kad gausiausiai dera ‘Ligol’ obelys su P 60 ir P 2 poskiepiais
(22,9–21,1 kg/vaism.). Obelys su þemiausiu P 22 poskiepiu dera ið esmës prasèiau
(11,0 kg/vaism.). Ið esmës augiausi ‘Ligol’ vaismedþiai yra su P 60 ir P 2 poskiepiais, o
produktyviausi – su P 22 poskiepiu. Ið esmës didþiausias vidutinis vaisiø derlius ið ploto
vieneto gautas auginant ‘Ligol’ veislës vaismedþius 4 x 2 m (1250 vaism./ha) atstumais su
P 2 ir P 60 poskiepiais – atitinkamai 26,4 ir 28,6 t/ha. Sumaþinus atstumus 0,5 m, vaismedþiø
su P 2 ir P 22 poskiepiais derlius ið esmës nepadidëjo. Vaismedþiai su stipresnio augumo
P 60 ir P 2 poskiepiais iðaugina ið esmës didþiausius vaisius ir jø masë nepriklauso nuo
sodinimo atstumo. Praktiniu poþiûriu versliniuose soduose geriausia auginti ‘Ligol’ veislës
vaismedþius su P 2 ar P 60 poskiepiais ir juos sodinti 4 x 1,5–2 m atstumais.
Reikðminiai þodþiai: augumas, derlius, obelys, poskiepiai, produktyvumas, sodinimo
schemos, vaisiø kokybë.
157
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 158–163.
PRELIMINARY EVALUATION OF APPLE TREE CULTIVAR
‘CELESTE’ ON DWARF ROOTSTOCKS IN CENTRAL
POLAND
Pavel BIELICKI, Alojzy CZYNCZYK, Barbara BARTOSIEWICZ
Research Institute of Pomology and Floriculture, 96-100 Skierniewice,
Poland. E-mail: [email protected]
The field experiment was established in the spring of 2001 in the Experimental Orchard
in Dabrowice, near Skierniewice, on a sandy loam podsolic soil underlaid by loam. The
influence of five dwarf apple rootstocks on tree growth, yield and fruit quality of the
cultivar ‘Celeste’ was studied. One-year-old maiden trees grafted on rootstocks PB-4,
P 59, P 60, P 14 and M.7 were planted at the same spacing of 3.5 x 2.0m (1429 trees/ha).
Trees grafted on M.9 and M.26 were used as standards.
After the first five years of the evaluation, Byelorussian rootstock PB-4 and Polish
rootstock P 59 were found to have induced the lowest growth of the cultivar ‘Celeste’.
The size of the trees on these two rootstocks was smaller than of those on the standard
M.9. Among the semi-dwarf rootstocks, trees on P 60 were smaller than those on the
standard M.26. Rootstock P 14 reduced tree growth to the same extent as M.7.
The highest cumulative yield (2002–2005) of ‘Celeste’ was recorded for trees on P 14,
M.26 and M.7. Trees grafted on P 60 and M.9 showed similar yields. The lowest yield was
obtained from trees on PB-4.
In 2005, the fruit quality parameters (size, mean weight, and colour) of cultivar ‘Celeste’
were generally very good with the exception of those harvested from trees on PB-4 and
P 59, which produced the smallest fruit.
Key words: apple, Malus sp., clonal rootstock, growth, yield, fruit quality, yield
efficiency.
Introduction. In recent years there has been a growing interest among fruitgrowers in summer varieties of apple. However, interest in such varieties is often
short-lived. The main reason is that they can be very disappointing in production and
the prices for this type of apples are highly changeable. Another problem is that there
is only a small assortment of summer cultivars. In comparison with the autumn or
winter cultivars, the number of cultivars in this group is quite small. At the end of
20th century, new summer varieties appeared, originating mainly from ‘Golden
Delicious’, the fruit of which was ready for consumption already in the first week of
August (Steinborn, 1983; Kruczyñska, 2002). ‘Celeste’ (syn. ‘Delcorf Schumann’)
158
is one of them. It came from Germany, where it was found by Schumann. ‘Celeste’
is one of two mutants of cultivar ‘Delcorf’ used in Poland. With respect to many
characteristics, it resembles the parent cultivar. Tree vigour, crown appearance as
well as susceptibility to diseases and productivity are all similar in both cultivars. It
requires fruitlet thinning to ensure regular fruiting. There is little difference in fruit
size between ‘Celeste’ and ‘Delcorf’, but the red blush on ‘Celeste’ apples is more
intense and spreads over a larger area of the skin. Fruit ripening time is similar to that
of ‘Delcorf’ (Goddrie, 1987). The share of ‘Celeste’ trees, and of the other mutant
‘Ambassy’, in the total number of apple trees produced in Poland has been growing
in recent years.
The aim of the experiment was to determine the usefulness of dwarfing
rootstocks for the growing of apple tree cultivar ‘Celeste’. An evaluation of seven
rootstocks with obvious differences in growth vigour should accurately single out
the best rootstocks for the production of trees of this cultivar in the soil conditions
of central Poland.
Material and methods. The field experiment was established in the spring of
2001 in the Experimental Orchard in Dabrowice, near Skierniewice (central Poland),
on a sandy loam podsolic soil underlaid by loam. The influence of five dwarfing
apple rootstocks on tree growth, yield and fruit quality of cultivar ‘Celeste’ was
studied. One-year-old maiden trees grafted on rootstocks PB-4, P 59, P 60, P 14 and
M.7 were planted at the same spacing of 3.5 x 2.0 m (1429 trees/ha). Trees grafted
on M.9 and M.26 were used as standards. The experiment was set up in four
randomized blocks with three trees per plot. Thus, there were 12 trees of cultivar
‘Celeste’ growing on each rootstock.
All the trees were trained as slender spindles and tied to a supporting structure.
Herbicides were used to control weeds in the tree rows, whereas the inter rows
were grassed over in the second year after planting. Fertilization, plant protection
and other agro-technical treatments were applied according to the standard
recommendations for commercial apple orchards in Poland. The trees were dripirrigated from the first year after planting.
In the course of the experiment the following observations and measurements
have been recorded: health status of trees, trunk circumferences (measured at
30 cm above ground level), yield (determined every year, separately for each tree)
and fruit quality (samples were taken from each replication). In 2005, fruit quality
was assessed using an electronic sorting machine manufactured by Greef. Statistical
analyses involved variance analyses and Duncan’s multiple range test at P = 0.05.
Results and discussion. T r e e h e a l t h. During the first five years of the
evaluation there was no loss of trees due to frost damage or infection with diseases.
Only 2 trees of ‘Celeste’ grafted on P 59 were lost due to falling over during periods
of strong winds while carrying the burden of a heavy crop. Similar observations
regarding the poor rooting ability of trees grafted on very dwarfing rootstocks were
made by Wertheim (1998) and Czynczyk et al. (2004).
Tree growth. After the first five years of the evaluation, Byelorussian rootstock
PB-4 (Ùukuã, 1994) and Polish rootstock P 59 were found to have induced the
lowest growth of cultivar ‘Celeste’ (Table 1). The size of the trees on these two
159
rootstocks was significantly smaller than of those on the standard M.9. Similar results
were obtained by Bielicki et al. (2004) for PB-4 with ‘Jonagold’ trees grafted on it
and Czynczyk et al. (2004) for P 59 with ‘Jonagold’ and ‘Ligol’ trees. Sùowiñski and
Sadowski (1999) reported that the vigour induced by PB-4 was similar to that of
M.27. Among the semi-dwarf rootstocks, trees on P 60 were smaller than those on
the standard M.26. In contrast, trees on P 14 were bigger than those on the standard
rootstock. The results confirmed earlier reports by Czynczyk (1995), Jakubowski
and Zagaja (2000) and Czynczyk et al. (2004), who stated that Polish rootstock P 14
showed a stronger effect inducing vigour than M.26. P 14 reduced tree growth to
the same extent as M.7. However, the results obtained by Hrotko and Berczi (1999)
showed that trees of cultivar ‘Idared’ on P 14 were bigger than trees on M.7.
T a b l e 1. Trunk cross-sectional area (TCA), yield and yield
efficiency of cv. ‘Celeste’ grown on dwarf rootstocks
1
l e n t e l ë.
‘Celeste’ veislës obelø su þemaûgiais poskiepiais kamieno
skerspjûvio plotas (KSP), derlius ir produktyvumas
Yield / Derlius
Rootstock
TCA in
2005
Poskiepis
KSP 2005 m.,
2002
2003
2004
2005
2
cm
Total yield
in 2002–
2005
Yield
efficiency
index (kg/cm2
Suminis derlius
TCA)
2002–2005 m.
Produktyvumas,
kg/cm2 KSP
kg/tree / kg/vaism.
M.9 standard
10.7 b
2.3 c
1.2 a
6.8 d
4.6 a
15.5 c
1.5 b
PB-4
5.0 a
1.4 b
0.8 a
2.8 b
1.9 a
6.8 a
1.4 ab
P 59
6.6 a
2.4 c
1.6 a
5.2 c
3.5 a
12.7 b
2.0 c
M.26 kontrolë
M.26 standard
19.6 c
0.7 a
5.9 c
1.0 a
16.9 cd
25.0 de
1.3 ab
P 60
11.7 b
0.5 a
4.0 b
1.4 ab
11.1 b
17.0 c
1.5 b
P 14
23.7 d
0.1 a
7.9 d
0.3 a
19.1 d
27.4 e
1.2 ab
M.7
23.4 d
0.7 a
6.3 c
1.4 ab
14.5 c
22.9 d
1.1 a
M.9 kontrolë
Averages followed by the same letter do not differ significantly at p = 0.05 (Duncan’s multiple
range test) / Ta paèia raide paþymëti vidurkiai pagal Dunkano kriterijø (p = 0,05) ið esmës nesiskiria.
Yields and Fruit Quality. The first yields from the cultivar ‘Celeste’ were obtained
in the second year after planting (Table 1). Very low yields (less than 1kg per tree)
were obtained from trees grafted on the semi-dwarf and medium vigorous rootstocks.
In the third year, the trees on those rootstocks produced bigger yields in comparison
with the trees on the dwarf rootstocks (M.9, PB-4 and P 59). Nevertheless better
yielding of the trees on the dwarf rootstocks was observed in the next year of fruitbearing. In 2005, the yielding situation was reversed. The trees on the semi-dwarf
and medium vigorous rootstocks gave higher yields. The highest cumulative yield
160
(2002–2005) was recorded for the ‘Celeste’ trees on P 14, M.26 and M.7. Trees
grafted on P 60 and M.9 showed similar yields. The lowest yield was obtained from
the trees on PB-4. The total yields obtained for the trees grafted on the very dwarfing
rootstocks were similar to those presented by Bielicki et al. (2004) and Slowinski
(2004).
The results concerning tree productivity, expressed as the yield efficiency index,
showed that the trees on P 59 were more productive than these on remaining
rootstocks. They had the highest yield efficiency index (expressed as ratio of yield
per tree to the trunk cross-sectional area (kg/cm2)). Similar values of this index were
obtained from the trees on the dwarf rootstocks. The trees on semi-dwarf rootstocks
(P 14 and M.7) had the lowest yield efficiency index.
In 2005, the size and weight of apples and the percentage of apples having more
than 50% of their skin surface covered by a red blush were similar for all the rootstocks
with the exception of fruits harvested from the trees on PB-4 and P 59 (Table 2). In
their case, fruits were significantly smaller. There were no statistical differences
between the rootstocks in respect of the colouring of the fruit. However, fruits on
P 59 were slightly worse coloured. These results are in agreement with the data
produced by Bielicki et al. (1999).
T a b l e 2. Fruit quality of cv. ‘Celeste’ grown on dwarf rootstocks in
2005
2
l e n t e l ë. ‘Celeste’ veislës obelø su þemaûgiais poskiepiais vaisiø kokybë 2005 m.
Rootstock
Poskiepis
Fruits with diameter >
7.0 cm
Fruits with blush on > 50%
of skin
14.3 ab
11.3 a
11.2 a
54.0 b
14.9 a
27.5 a
62.9 a
73.8 a
46.0 a
15.4 b
14.2 ab
15.5 b
15.9 b
74.2 b
58.3 b
72.4 b
78.3 b
71.6 a
70.4 a
58.4 a
71.4 a
Weight of 100 fruits
100 vaisiø masë, kg
Vaisiai, kuriø skersmuo
> 7,0 cm, %
Vaisiø, kuriø odelë
> 50% paraudusi, %
M.9 standard
M.9 kontrolë
PB-4
P 59
M.26 standard
M.26 kontrolë
P 60
P 14
M.7
For explanation, see Table 1 / Paaiðkinimus þr. 1 lentelëje
Conclusions. 1. The lowest growth of apple tree cultivar ‘Celeste’ was induced
by Byelorussian rootstock PB-4 and Polish rootstock P 59.
2. Growth vigour of the trees of cultivar ‘Celeste’ grafted on P 60 was similar
to those on M.9 EMLA.
3. P 14 was similar to M.7 in its ability to reduce tree growth.
4. The highest cumulative yield was obtained from the trees of cultivar ‘Celeste’
grafted on the semi-dwarf rootstocks P 14 and M.7.
161
5. The highest yield efficiency index was obtained for the trees of cultivar
‘Celeste’ growing on the very dwarf Polish rootstock P 59. In the case of semidwarf rootstocks, all of the trees were characterized by a similar yield efficiency
index.
6. The development of fruit quality parameters (with the exception of fruit size)
appeared to be unaffected by the rootstock type. The smallest apples of cultivar
‘Celeste’ were harvested from trees on the very dwarf rootstocks.
Gauta
2006 07 05
Parengta spausdinti
2006 07 17
References
1. B i e l i c k i P., C z y n c z y k A., B a r t o s i e w i c z B. Effects of New
Polish Rootstocks and Some M 9 Clones on Growth, Cropping and Fruit Quality of Three
Apple Cultivars. Proc. of the International Seminar “APPLE ROOTSTOCKS FOR
INTENSIVE ORCHARDS”. Warsaw-Ursynów, 1999. P. 15–16.
2. B i e l i c k i P., C z y n c z y k A., C h l e b o w s k a D. Effects of Several
New Polish Rootstocks and M.9 Subclones on Growth, Yield and Fruit Quality of Two
Apple ‘King Jonagold’ and ‘Elshof’ Cultivars. Acta Hort. 2004. 658. P. 327–332.
3. C z y n c z y k A. New apple rootstocks from the Polish Breeding Program.
International. Dwarf Fruit Tree Association, Pennsylvania. Compact Fruit Tree. 1995. Vol.
28. P. 68–76.
4. C z y n c z y k A., B i e l i c k i P., B a r t o s i e w i c z B. Influence of
Subclones of M.9 and P 22 and New Polish-Bred Rootstocks on Growth and Yield of
‘Jonagold’ and ‘Ligol’ Apple Trees. Acta Hort. 2004. 658. P. 129–133.
5. G o d d r i e P. D. Delbarestivale. Fruitteelt. 1987. 77(43). P. 16–17.
6. J a k u b o w s k i T., Z a g a j a S. W. 45 years of apple rootstocks breeding
in Poland. Proc. of the Eucarpia Symp. of Fruit Breeding and Genetics. Acta Hort. 2000.
538. P. 723–727.
7. H r o t k o K., B e r c z i J. Effect of semi-dwarfing and medium vigorous
rootstocks on growth and productivity of apple tress. Proc. of the International Seminar
„Apple Rootstocks for Intensive Orchards”. Warsaw-Ursynów., 1999. P. 35–36.
8. K r u c z y ñ s k a D. JABÙONIE – nowe odmiany. Wyd. Hortpress Sp. z o.o.
2002. P. 25–36.
9. Ù u k u ã T. PB-4 – obiecujàca podkùadka dla jabùoni. Sad Nowoczesny. 1994.
(7). 9 p.
10. S a d o w s k i A., G r o c h o w a l s k i W., S ù o w i ñ s k i A. and
Ý ó ù t o w s k i J. Ocena siùy wzrostu jabùoni na podkùadce PB-4. Zesz. Nauk. Inst. Sad.
i Kw. Skierniewice. 2002. 8. P. 71–76.
11. S ù o w i ñ s k i A., S a d o w s k i A. Growth in the nursery and in the orchard
and initial bearing of ‘Elise’ apple trees on different rootstocks. Proc. of the International
Seminar „APPLE ROOTSTOCKS FOR INTENSIVE ORCHARDS”. Warsaw-Ursynów, 1999.
P. 99–100.
12. S ù o w i ñ s k i A. Comparison of 22 Rootstocks of Different Vigour Used for
‘Elise’ Apple Trees. Acta Hort. 2004. 658. P. 279–286.
162
13. Steinborn G. New early apple cultivars compared. Erwerbsobstbau. 1983. 25(8).
P. 188–190.
14. W e r t h e i m S. J. Rootstock guide. Fruit Res. St. Wilhelminadorp Publ.
1998. No. 25.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
158–163.
PRELIMINARUS ‘CELESTE’ VEISLËS OBELØ SU ÞEMAÛGIAIS
POSKIEPIAIS ÁVERTINIMAS CENTRINËJE LENKIJOJE
P. Bielicki, A. Czynczyk, B. Bartosiewicz
Santrauka
2001 metø pavasará tyrimø sode Dabrovicuose, netoli Skiernievicø, priesmëlio jaurinëje
dirvoje ant priemolio atliktas lauko bandymas. Tirta penkiø þemaûgiø obelø poskiepiø
átaka ‘Celeste’ veislës vaismedþiø augimui, derliui ir vaisiø kokybei. Vieneriø metø sodinukai,
áskiepyti á PB-4, P 59, P 60, P 14 ir M.7 poskiepius, buvo pasodinti vienodais atstumais –
3,5 x 2,0 m (1429 medþiai/ha). Á M.9 ir M.26 áskiepyti vaismedþiai panaudoti kaip kontrolë.
Praëjus pirmiesiems penkeriems tyrimo metams pastebëta, kad baltarusiðkas poskiepis
PB-4 ir lenkiðkas poskiepis P 59 labiausiai stabdo ‘Celeste’ veislës augimà. Vaismedþiai su
ðiais poskiepiais buvo þemesni uþ vaismedþius su M.9. Pusiau þemaûgiø poskiepiø grupëje
vaismedþiai su P 60 buvo þemesni uþ vaismedþius su M.26 poskiepiu. P 14 poskiepis
sumaþino vaismedþiø augimà tiek pat, kiek ir M.7.
2002–2005 m. didþiausià suminá derliø davë ‘Celeste’ veislës vaismedþiai su P 14,
M.26 ir M.7 poskiepiais. Panaðø derliø iðaugino á P 60 ir M.9 áskiepyti vaismedþiai.
Nederlingiausi buvo vaismedþiai su PB-4.
2005 metais ‘Celeste’ veislës obuoliø kokybë (dydis, vidutinë masë ir spalva) ið
esmës buvo labai gera, iðskyrus nuskintus nuo vaismedþiø su PB-4 ir P 59 poskiepiais –
ðie vaisiai buvo maþiausi.
Reikðminiai þodþiai: obuoliai, Malus sp., vegetatyviniai poskiepiai, augimas, derlius,
vaisiø kokybë, produktyvumas.
163
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 164–172.
SEARCH FOR A MORE DWARFING ROOTSTOCK FOR
‘JONAGOLD’
Jef VERCAMMEN*, Guy VAN DAELE and Ann GOMAND
Pcfruit - Proeftuin pit- en steenfruit, Fruittuinweg 1, 3800 Sint-Truiden,
Belgium. E-mail: [email protected]
Up until now we did not find a better rootstock than M.9 in our rootstock experiments.
Nevertheless there are a couple of promising rootstocks for ‘Jonagold’, namely J.TE.G.
and P 16. J.TE.G. is 15% less vigorous than M.9. The production efficiency and colouring
remain the same, but there are more kilos of A2++ in the 70–85 mm size class because of its
smaller fruit size. P 16 is 30% less vigorous. The colouring and the production are almost
comparable to those of M.9 and over the years the fruit size remains somewhat smaller on
average. The combination of the lesser vigour and the same yield causes the production
efficiency of P 16 to be clearly better than that of M.9-29.
Where the vigour of M.9 is too strong, other selections of M.9 with less vigour can
be used. The most suitable selections to this purpose are M.9 Fl56, NAKB 337 and
NAKB 339. M.9 Fl56 has the weakest growth and the fruit size can be compared to that of
M.9-29. With respect to colouring, there is no improvement.
Also the use of M.27 as rootstock springs to mind, but M.27 is not always suited to
replace M.9. In many cases a tree with vigour between M.9 and M.27 is needed. One
possibility to achieve this is the use of M.27 as interstock, in the hope that the advantages
of M.9 (production and size) and of M.27 (colour and labour) will be found in the interstock
tree. In practice however this does not seem to be so.
Another possibility is the use of Granny Smith, Delcorf or Idared as interstock.
These interstocks provide a clear growth reduction, without influencing the yields too
much.
Key words: interstock, M.27, M.9-selections, M.9 Fl56, J.TE.G and P 16.
Introduction. For most fruit growers the ideal tree is a tree that does not grow
to vigorously, demands little labour and yields a good production and high quality
every year. In order to achieve this, our varieties are grafted or inoculated on a
rootstock. For the Belgian apple culture this is mostly M.9, a rootstock with moderate
vigour. Though M.9 satisfies in most cases, there are conditions where trees with
less vigour are needed.
First the use of M.27 as rootstock springs to mind. Because of its weak vigour
less pruning hours per ha are needed, which is an important advantage, taking into
account current labour costs. Other advantages are the better colouring and, in the
164
case of varieties with big fruits, a smaller fruit size. Moreover the intensifying also
raises fewer problems.
Unfortunately M.27 also has some drawbacks. The sometimes quickly declining
growth does make M.27 sometimes less suitable and in many cases unsuitable for
replanting. Fertilization also has to be adapted, M.27 needs more nitrogen, phosphorus
and potassium than M.9. Furthermore the trees are more expensive and they do
easily break off at the graft union. In order to obtain the same produce per ha, more
trees have also to be planted per ha, which strongly raises the investment costs
(Vercammen, 1997).
Because of this M.27 is not always suitable to replace M.9. In many cases a
tree of which the vigour lies between that of M.9 and M.27 is needed. In this paper
we will discuss some possibilities to achieve this aim.
Materials and methods. Use of an interstock. In the autumn of 1997 an
interstock experiment for the ‘Jonagold’ clone ‘Jonica’ was started. Besides M.27,
P 22 and Bud 146 also a number of varieties were used as interstock. In the Netherlands
(Bal) they had very good experiences with the use of Summerred as an interstock
for Elstar (Baab) and from everyday practice it was said that the use of Elstar as an
interstock for ‘Jonagold’ has a better colouring for a result. Other interstocks included
in the experiment are: Gloster, Golden, Granny Smith, Idared, Delcorf, Braeburn,
Gala, Red Chief and Zoete Aagt. Knipbomen were added as a control to the experiment.
For each combination 3 replicates of 6 trees were planted. A planting distance of
3.50 x 1.50 m (1.714 trees/ha) was observed for all trees.
Use of other rootstocks. The following rootstocks were chosen for a comparative
rootstock experiment: the Polish rootstocks P 59 and P 60, the Russian rootstocks
Budagovski 9, 146 and 491, the Czech rootstocks J.TE.E, J.TE.F and J.TE.G and
the German rootstocks Pi80 (Supporter 4), PiAu733 and PiAu916. These rootstocks
were compared to M.9T337 and M.27. The test variety was ‘King Jonagold’ and
the planting distance was 3.50 x 1.40 m (1.837 trees/ha). For each combination 12
trees were planted in December 1996. The experiment was followed for 6 years and
attention was mainly paid to vigour, production, fruit size and colouring.
Different M9-selections. In the year of planting 1999–2000, 10 different
selections of M.9 were planted for ‘Novajo’, namely M.9 F156, M.9 1576, M.9-8,
M.9-19, M.9-29, NAKB 337, NAKB 339, Burgmer 984 and Pajam 2. A number of
rootstocks with weak vigour were also planted, namely M.27, P 22, P 16 and
Budagovski 9. For each rootstock 4 replicates of 5 trees were planted. Braeburn
was chosen as pollinator (9 % scattered through the rows). The planting distance
for all trees was 3.50 x 1.25 m (2.057 trees/ha). From 2001 attention was mainly
paid to vigour, production, fruit size and colouring.
Results and discussion. Use of an interstock. V i g o u r. As a measure for
the vigour the increase in trunk circumference from 1998 up to and including 2005
was used (measured just below the first branching). From this it clearly appeared
that the experiment can be divided into two groups, depending on the vigour. When
a Gloster, Golden, Braeburn, Gala or Red Chief interstock is used for ‘Jonica’, the
vigour equals that or is somewhat stronger than that of the Knipbomen. The vigour
is clearly stronger when Elstar is used as interstock. From figure 1 it appears that
165
the vigour of a Bud 146 interstock can be compared to that of a M.27 interstock. On
the other hand the vigour provoked by P 22 is even weaker than that of M.27.
A Delcorf interstock also provokes a clearly smaller increase in trunk circumference,
but the trees are clearly more vital than those with a M.27, P 22 or Bud 146 interstock.
Summerred, Idared, Granny Smith and Zoete Aagt provoke an increase in trunk
circumference between the Knipbomenand M.27.
Y i e l d d a t a. The differences in production between the more vigorous
interstocks are only small. Only for a Golden interstock the production per tree did
remain smaller almost every year. Concerning the fruit weight there are no significant
differences either, although with Gala there is a tendency to smaller fruits. On the
other hand there are big differences in production in case of the weaker interstocks
(Table 1). Only Idared obtains approximately the same level as the Knipbomen each
year. All other interstocks are clearly less productive than the Knipbomen. In particular
when a M.27, P 22 or Bud 146 interstock is used the production remains undersized.
This can for the most part be explained by the lack of vigour of these trees.
T a b l e 1. Yield data of ‘Jonica’ with different interstocks (Pcfruitpps, 1999–2005)
1
l e n t e l ë.
Interstock
Intarpas
Knipbomen
M.27
P 22
Bud 146
Summerred
Granny Smith
Idared
Delcorf
Zoete Aagt
‘Jonica’ veislës derlius, naudojant skirtingus intarpus, 1999–2005 m.
Kg/tree / Kg/medis
2005
43.5
28.0
17.2
27.2
40.6
37.9
42.5
37.1
33.9
1999–2005
a
f
g
f
c
d
b
e
f
Kg/cm
trunk circumference
kamieno apimtis
187.1
127.9
91.3
123.1
162.7
168.5
176.8
165.1
169.2
8.5
7.8
6.7
7.3
8.5
8.8
9.4
9.1
8.8
Fruit weight / Vaisiaus masë, g
2005
241
162
154
180
195
212
202
210
255
b
d
d
cd
c
c
c
c
a
1999–2005
254
212
208
212
230
233
228
227
248
To calculate the effect of the vigour, the yield is also expressed per unit of
growth in table 1. As a measure for growth the trunk circumference of end 2005
was chosen. The best results are obtained by Idared, with a production efficiency
that is even better than that of the Knipbomen. For an important part this due to its
weaker vigour (Figure 1). Other interstocks with a better score than the Knipbomen
are Delcorf, Granny Smith and Zoete Aagt. After 7 years of production P 22 and Bud
146 obtain the lowest production efficiency. As mentioned above, this can mainly be
explained by the insufficient vitality of these trees.
On average over the years, the fruit size of all weaker growing interstock trees
is clearly smaller than that of the Knipbomen. In years with too big sized fruits, e.g.
2002, 2003 and 2004, this is positive. In 2001 and 2005 on the other hand, when the
average fruit size was clearly smaller, trees with a M.27, P 22 or Bud 146 interstock
166
produced fruits that were too small. In this case also the insufficient vitality of the
trees played an important role.
T a b l e 2. Yield data of ‘King Jonagold’ on different rootstocks
(Pcfruit-pps, 1998–2002)
2
l e n t e l ë.
Rootstock
Poskiepis
‘King Jonagold’ veislës su skirtingais poskiepiais derlius 1998–2002 m.
Yield / Derlius 1998–2002 m.
kg/tree / kg/medis
%
92.5
66.4
67.4
65.8
75.3
84.9
71.7
76.3
100.0
71.8
73.0
71.2
81.5
91.9
77.5
82.6
M.9T337
M.27
PiAu916
PiAu733
B.491
B.146
P 59
J.TE.G
Kamieno apimtis
Fruit weight
g
1998–2002
4.7
4.1
4.4
4.3
4.3
4.9
5.0
4.7
249
221
190
193
223
229
219
223
Kg/cm
trunk circumference
Vaisiaus masë,
T a b l e 3. Yield data of ‘Novajo’ on different M.9-selections
(Pcfruit-pps, 2001–2005)
3
l e n t e l ë.
‘Novajo’ veislës su skirtingais M.9 klonais derlius 2001–2005 m.
Trunk circumference
Kg/tree / Kg/medis
Rootstock
Poskiepis
Kamieno apimtis
2005
2005 m., cm
Kg/cm
trunk
2001–2005 kamienas
Fruit weight
g
2002–2005
Vaisiaus masë,
M.9-selections / M.9 klonai
M.9-29
19.1 ab
38.9 ab
107.7
5.6
245
M.9-19
19.2 a
36.3 b
100.9
5.3
246
M.9-8
19.8 a
36.3 b
105.1
5.3
254
M.9 1576
19.8 a
38.9 b
112.7
5.7
254
M.9 Fl56
16.9 b
33.7 a
106.5
6.3
247
NAKB 337
17.7 b
37.5 b
109.1
6.2
234
NAKB 339
18.3 b
37.1 b
111.4
6.1
242
Burgmer 984
19.7 a
40.0 a
107.0
5.4
250
Pajam 2
19.1 a
35.8 b
102.3
5.4
240
Dwarfing rootstocks / Žemaûgiai poskiepiai
M.27
15.5 b
19.6 b
74.1
4.8
206
P 22
13.1 c
18.7 c
63.9
4.9
207
P 16
14.4 b
28.6 b
94.7
6.6
227
Bud 9
16.3 b
28.0 b
76.5
4.7
226
167
1
F i g. 1. Increase in trunk circumference of ‘Jonica’ with different interstocks
(Pcfruit-pps, 1998–2005)
p a v. ‘Jonica’ veislës vaismedþiø kamienø apimtis, naudojant skirtingus intarpus,
1998–2005 m.
C o l o u r. A third aspect that is important when choosing an interstock is the
influence on the colouring. With respect to the share at first picking over the 7 years
not one interstock with weak vigour obtains a bigger first picking than the Knipbomen.
The number of A2++ kilos also remains smaller than in case of the Knipbomen. The
number of kilos at first picking and the number of kilos A2++ produced by the
vigorous interstocks usually is not any bigger than those produced by the Knipbomen
either. Only a Gloster or Elstar interstock obtains a somewhat better colouring during
the 7 years.
However if we take a look at the number of kilos A2++ in the 70–85 mm size
class, a totally different picture presents itself (Figure 2). Over the 7 years and in
total the trees with a Granny Smith, Idared, M.27 or Delcorf interstock obtained the
most kilos in the most interesting size classes from a commercial point of view.
Here also the worst results were obtained by P 22 and Bud 146.
F i g. 2. Colouring of ‘Jonica’ with different interstocks (Pcfruit-pps, 1999–2005)
2
p a v.
‘Jonica’ veislës vaisiø spalva, naudojant skirtingus intarpus, 1999–2005 m.
168
Use of other rootstocks. V i g o u r. The list below contains the different
rootstocks in proportion to their vigour. As a measure for the vigour the increase in
trunk circumference from 1997 up to and including 2002 was used.
– Stronger vigour than M.9T337
* Pi80 (Supporter 4): vigour is too strong (30% more than M.9T337)
– Vigour equal to that of M.9T337
* Bud 9 and P 60: comparable vigour
* J.TE.E and J.TE.F: 5 to 10 % less vigour than M.9T337
–Vigour between M.9T337 and M.27
* Bud 146 and Bud 491: cause a growth inhibition of 10%
* J.TE.G: 15 % less vigour than M.9T337
–Vigour equal to or weaker than that of M.27
* PiAu916 and PiAu733: vigour comparable to that of M.27
* P 59: 10% less vigour than M.27
Y i e l d d a t a. As appears from table 2, from 1996 up to 2002 the highest
total yield was obtained by M9T337, followed by Bud 146. The difference amounts
to about 10%. The other rootstocks with weak vigour are approximately 20% less
productive than M.9T337. After 5 years of production all rootstocks with strong
vigour also obtain a smaller yield than M.9T337. When we take a closer look at the
production efficiency, we see that P 59 obtains the best result, followed by Bud 146
and J.TE.G. (As a measure for growth the trunk circumference of end 2002 was
chosen.) The production efficiency of all other rootstocks was less good than that
of M.9T337.
Concerning the fruit size all rootstocks, except for Pi80, produce smaller sized
fruits than M.9T337. This is an important advantage, especially for ‘Jonagold’. As
is the case for the interstocks with weak vigour, a warning is in place that in some
years rootstocks with weak vigour can produce too small sized fruits. In 2001 the
average fruit weight of PiAu916 and PiAu733 amounted to 152 and 154 respectively,
with for a consequence that 30 to 35% of the yield was smaller than 70 mm. That
year the fruit of the other rootstocks weighed between 180 and 200 grams on average.
For M.9 this was 213 grams.
C o l o u r. Whether the colouring of ‘Jonagold’ grafted on the rootstocks
with weak vigour is good or not, strongly depends on the number of apples per tree.
This can be explained for the most part by the smaller trees and the relatively big
number of apples per tree, which provokes a less favourable leaf/fruit-balance.
When we look at the number of kilos A2++ (Figure 3) we see that here also
M.9T337 and J.TE.G obtain the best results, but the differences with the other
rootstocks are less outspoken. In case of the rootstocks with strong vigour the
differences are even smaller. Only J.TE.E obtains fewer kilos A2++. However this
can be explained by the small yields obtained by this rootstock.
When we limit ourselves to the number of kilos A2++ in the 70–85 mm size
class, a totally different picture presents itself. All rootstocks, except for Pi80,
obtain a bigger number of kilos in the commercially most interesting size classes.
For the rootstocks with weak vigour PiAu916, PiAu733 and M.27 obtain the best
results. On the other hand Bud 491 and Bud 146 clearly did less good, but the
169
number of kilos A2++ in the 70–85 mm size class still remains bigger than with
M.9T337.
F i g. 3. Colouring of ‘King Jonagold’ on different rootstocks (Pcfruit-pps,
1998–2002)
3
p a v.
‘King Jonagold’ veislës vaisiø spalva, naudojant skirtingus poskiepius,
1998–2002 m.
Different M9-selections. The growth of M.9 F156, NAKB 337 and NAKB 339
is weaker than that of M.9-29. The trunk circumference of the other selections are
somewhat larger. The yield of most selections equal that or are larger than that of
M.9-29. Only M.9-19 and Pajam 2 have a smaller yield. On the other hand the
production efficiency of M.9 Fl56, NAKB 337 and NAKB 339 is better than that of
M.9-29. The fruit weight is also at least as big. NAKB 337 is the only selection with
on average slightly smaller fruits.
In many cases the colouring of the different selections was disappointing. After
all none of these selections obtains a bigger first picking or more kilos A2++ after
5 years of production. All this indicates that for now M.9 F156 and both NAKBnumbers, turn out to be the best selections of M.9.
From the rootstocks with weak vigour P 16 turn out to be the best after 5 years
of production. Of P22 it is known that in the year of planting one should be very
careful in case of a drought. The vigour of P16 is weak, but it still obtains a yield
only slightly smaller than that of M.9-29. Because of this the production efficiency is
clearly better than that of M.9-29. All rootstocks with weak vigour produce a smaller
fruit size, which is certainly positive in case of ‘Jonagold’. With respect to the share
of A2++ in the 70–85 mm size class, M.27 and especially P 22 turn out to be the
best, but not as good as M.9-29.
After five years there already can be distinguished some distinct tendencies.
The following years this experiment will be followed further in order to examine
whether these tendencies are confirmed or not.
Conclusion. Overall it is safe to put that M.9 remains a good rootstock. Up
until now we did not find a better rootstock in our rootstock experiments. However
there are a couple of promising rootstocks for ‘Jonagold’, namely J.TE.G and
P16. J.TE.G is 15% less vigorous than M.9. Production efficiency and colouring
170
are the same, but because of its smaller fruit size there are more kilos A2++ in the
70–85 mm size class. P 16 is 30% less vigorous. The combination of the lesser
vigour and the same yield causes the production efficiency of P 16 to be clearly
better than that of M.9-29.
Where the vigour of M.9 is too strong, the less vigorous selections of M.9 can
also be used. The most suitable selection for this are M.9 F156, NAKB 337 and
NAKB 339. These selections show the least growth and the fruit size equals that of
M.9-29. Concerning the colouring however, there is no improvement. However,
further research into the matter is still necessary.
The use of M.27 as interstock holds too many risks to be advisable. In some
cases the vigour is even less than when M.27 is used as rootstock. The interstock
trees have a tendency to stagnate after 4 or 5 years. This causes the fruits to remain
too small and the colouring to diminish year after year.
The use of Idared, Granny Smith or Delcorf as interstock can be an option.
These interstocks clearly cause a reduction of the growth, without influencing the
yields too strongly. Through this the production efficiency is even better than in case
of the Knipbomen on M.9. A further advantage is that the fruits weigh 20 to 25
grams less on average. On the other hand the colouring does not appear any sooner
and the number of kilos A2++ is not bigger than in case of the Knipbomen. However,
seeing that the fruit size is considerably smaller, the number of kilos A2++ in the 70–
85 mm size class is clearly bigger than that of the Knipbomen. If these results are
confirmed in the following years, these interstocks could form interesting alternatives.
Gauta
2006 04 28
Parengta spausdinti
2006 08 07
References
1. B a a b G. Summerred - die Zwishenveredlung für Elstar? “Obstbau 10”. 1998.
531–534.
2. B a l J. Summerred, de “tussen”-oplossing bij groeibeheersing. “Fruitteelt”
86(30).1996.14–15.
3. V e r c a m m e n J. Wat is de waarde van M27 als tussenstam? “Belgische
Fruitrevue” 49(02). 1997. 9–11.
4. V e r c a m m e n J. Welke nieuwe onderstam doet beter dan Bud 146? “Belgische
Fruitrevue” 50(02). 1998. 29-32.
5. P C F - P P S, 2002. Annual report “PCF-Proeftuin Pit- en Steenfruit”. P. 113–123.
6. P C F - P P S, 2005. Annual report “PCF-Proeftuin Pit- en Steenfruit”- Appel.
P. 189–193.
7. P C F - P P S, 2005. Annual report “PCF-Proeftuin Pit- en Steenfruit”- Appel.
P. 194–202.
171
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
164–172.
‘JONAGOLD’ VEISLEI TINKAMØ ÞEMAÛGIØ POSKIEPIØ TYRIMAS
J. Vercammen, G. Van Daele, A. Gomand
Santrauka
Atliekant tyrimus su poskiepiais mûsø ðalyje, geresnio uþ M.9 poskiepio iki ðiol
nerasta. Du perspektyvûs ‘Jonagold’ veislei tinkami poskiepiai – J.TE.G. ir P16. J.TE.G. yra
15% maþiau augûs uþ M.9, produktyvumas ir spalva iðlieka tie patys, bet 70–85 mm dydþio
vaisiø grupëje dël to, kad joje yra maþesni vaisiai, esama daugiau A2++ kokybës vaisiø.
P 16 poskiepis yra 30% maþiau augus uþ M.9, spalva ir produktyvumas beveik prilygsta
M.9, o vidutinis vaisiø dydis per daugelá metø iðlieka truputá maþesnis. Maþesnio augumo
ir tokio pat derliaus derinys lemia tai, kad P 16 produktyvumas yra kur kas didesnis negu
M.9-29.
Kai M.9 augumas yra per didelis, galima naudoti kitus, ne tokius augius, M.9 klonus.
Ðiam tikslui tinkamiausi M.9 Fl56, NAKB 337 ir NAKB 339 klonai. Silpniausiai auga M.9Fl56,
jo vaisiø dydis prilygsta M.9-29, spalva nepagerëja.
Galima naudoti ir M.27 poskiepá, taèiau jis ne visada tinka M.9 poskiepiui pakeisti.
Daugeliu atvejø reikalingas vaismedis, kurio augumas bûtø tarpinis tarp M.9 ir M.27.
Vienas ið bûdø tai pasiekti yra panaudoti M.27 kaip intarpà, tikintis, kad vaismedis ágis ir
M.9 (derlingumas ir dydis), ir M.27 privalumø (spalva ir maþesnës darbo sànaudos). Taèiau
praktiðkai tai padaryti nepavyksta.
Dar viena galimybë – kaip intarpus panaudoti Granny Smith, Delcorf arba Idared. Jie
uþtikrina augimo sumaþëjimà, pernelyg nepaveikdami derliaus.
Reikðminiai þodþiai: intarpas, M.27, M.9 klonai, M.9 Fl56, J.TE.G ir P 16.
172
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 173–180.
GROWTH AND YIELDING OF ‘JONAGOLD’ AND ‘LIGOL’
APPLE TREES ON M.9 AND P 22 SUBCLONES, AND
SOME OTHER POLISH ROOTSTOCKS
Alojzy CZYNCZYK, Pawel BIELICKI, Barbara BARTOSIEWICZ
Research Institute of Pomology and Floriculture 96-100 Skierniewice,
Pomologiczna str. 18, Poland. E-mail: [email protected]
The effect of subclones of M.9 (M.9T 337, Pajam 1, RN 29), P 22 (P 22/K, P 22/A,
P 22/J), and some new Polish rootstocks (P 59, P 60, P 61 and P 62) on the growth and
yielding of ‘Jonagold’ and ‘Ligol’ apple trees was studied in a field experiment over a
period of 10 years. The vigour of both cultivars on subclones M.9 was very close to that
on the standard rootstock M.9 EMLA, but trees on Pajam 1 were the smallest. Trees
‘Jonagold’ grafted on the new Polish rootstock P 62 were significantly less vigorous than
those on M.9 EMLA. Tree vigour of both cultivars on the subclones of P 22 was similar to
that on the standard rootstock P 22. ‘Jonagold’ trees grafted on P 61 were significantly
smaller than the standard trees on P 22. The smallest trees of both cultivars were obtained
on P 59. In the group of semi-dwarfing rootstocks, the smallest trees were on P 60 and the
largest on P 14. Yields were more or less proportional to tree size. Among the subclones of
P 22, the highest cumulative yields for both cultivars were obtained on P 22/A. The
highest cumulative yields for both cultivars on the M.9 subclones were obtained on M.9T
337 and, in the semi-dwarfing group, for ‘Jonagold’ trees on P 60 and ‘Ligol’ trees on P 14.
The values of the yield efficiency index for the subclones of M.9 were similar to those for
M.9 EMLA, and among the subclones of P 22 the values of this index were similar to those
for the standard P 22 rootstock. The highest yield efficiency index among the semi-dwarfing
rootstocks was obtained for P 60. In 2004, the fruit quality parameters, such as size, weight
and the percentage of fruits with a blush on more than 50% of the skin surface, were very
good for both cultivars on most of the rootstocks and similar to the quality parameters of
the fruits on the standard rootstocks. ‘Jonagold’ apples of a significantly smaller size were
obtained on P 59.
Key words: apples, rootstocks, subclone, growth, yielding efficiency, fruit quality.
Introduction. One of the most efficient ways of obtaining early yielding of
apple trees in modern orchards is to plant dwarf trees (Czynczyk, 1995 and 2000;
Mika, 1995). Such trees can be obtained by using dwarfing rootstocks for their
production. There is, however, no universal rootstock for all kinds of soil, climatic
conditions or various apple cultivars. On light soils (the predominant type of soil in
Poland), these requirements are satisfied grafting trees on semi-dwarfing rootstocks
173
such as M.26, P 14 and P 60 (Bielicki et al., 1999; Czynczyk, 1995; Czynczyk and
Piskor, 2000; Skrzyñski and Poniedziaùek, 1999). However, trees grafted on these
rootstocks often grow too strongly (vigorously) on more fertile soils. Rootstock
M.9, the most commonly used rootstock in the countries of Western Europe, is also
recommended for growing in Polish conditions (Czynczyk et al., 2001). However,
growing of trees on this rootstock is associated with some dangers. For example,
the root system of trees growing on M.9 could be damaged by low temperatures
during winters without snow. Trees on P 22, on the other hand, are more winter
hardy, but they need more fertile soil, irrigation and very well thinned fruitlets to
produce good quality fruits. So far the usefulness of the subclones of the M.9 and
P 22 rootstocks growing the more economically important apple cultivars in Poland
(‘Jonagold’ and ‘Ligol’) has not been tested over a longer period of time. Can trees
grafted on the subclones of M.9 and P 22, and growing on light soils, bear fruits of
good quality in older age? The aim of the study presented here was to determine the
orchard performance of ‘Jonagold’ and ‘Ligol’ apple cultivars grafted on different
rootstocks, mainly on subclones of the two rootstocks, M.9 and P 22. In this trial,
we determined their adaptability to the variable conditions of Poland’s climate, paying
particular attention to tree health and vigour, crop abundance and fruit quality in
older age.
Materials and methods. The trial began in the autumn of 1994 at the Experimental
Orchard of the Research Institute of Pomology and Floriculture in Dàbrowice, central
Poland. One-year-old maidens grafted on subclones of M.9 and P 22 rootstocks, and
also on the dwarfing rootstocks: P 14, P 59, P 60, and P 61, P 62 recently bred by the
Institute of Pomology and Floriculture (Zagaja et al., 1991; Jakubowski, 1999). All
rootstocks were classified into three groups. The first group consisted of trees on
P 59, P 61 and P 22 (as standard) and its three subclones: P 22/K (mother plants
propagated in vitro, rootstock intermediate in character), P 22/A (an adult subclone
with poor rooting ability, without spines in stoolbeds) and P 22/J (juvenile subclone
with very good rooting ability, a few spines and significantly higher number of layers
in stoolbeds (List of cultivars, 1977). The second group consisted of various
subclones of M.9 and P 62, whilst the third group included semi-dwarfing rootstocks:
P 14, P 60 and M.26 (Table 1).
The control function was performed by trees grafted on the P 22, M.9 EMLA and
M.26 rootstocks commonly used in the production of apple trees in Poland. The orchard
was located on a sandy loam podsolic soil underlaid by loam. Experimental trees were
planted according to a randomized block design with 3 sub-blocks for each cultivar, in
4 replications and 3 trees per plot. Trees were trained in the slender spindle bush
system. The following observations and measurements were recorded: health status
of trees, trunk circumference, yield size and fruit quality. The results were statistically
analyzed using the variance analysis method. To assess the significance of the differences
between means, Duncan’s t-test was used at the 5% level of significance. The
significance of the differences was assessed separately for the rootstock sub-blocks,
which represented the specific groups of rootstocks (Table 2).
174
T a b l e 1. Trunk cross-sectional area (TCSA), yield, yield efficiency
and quality of fruits of cv. ‘Jonagold’ grown on subclones
of M.9 and P 22, and some Polish-bred rootstocks
1
l e n t e l ë. ‘Jonagold’ veislës obelø su M.9 ir P 22 subklonais ir kai kuriais
lenkiðkos kilmës poskiepiais kamieno skerspjûvio plotas (KSP),
derlius, produktyvumas ir vaisiø kokybë
Amount of
Number of
fruits with
Total yield, Yield
Weight
lost trees TCSA in
diameter
1996–2004 efficiency of 100
from 12
2
>7 cm
2004
(kg/cm
(kg/tree)
fruits
Rootstocks
plants
KSP
Suminis
TCSA) 100 vaisiø Vaisiø, kuriø
Poskiepiai
Þuvusiø
skersmuo
2004 m., derlius 1996– Produktyvumasë, kg
medþiø
>7 cm, kiekis,
2004 m.,
cm2
mas, kg/cm2
skaièius iš
g/medis
%
KSP
12 sodinukø
P 22*
P 22/K
P 22/A
P 22/J
P 59
P 61
M.9 EMLA*
M.9 T337
M.9 Pajam 1
M.9 RN 29
P 62
M.26*
P 14
P 60
0
0
0
0
1
1
0
1
0
1
0
1
0
0
56.6 c
52.2 c
59.1 c
54.9 c
16.4 a
39.7 b
76.0 b
78.0 b
70.0 b
77.7 b
55.4 a
99.2 b
118.3 c
80.7 a
145.4 b
149.5 b
162.4 b
156.6 b
71.2 a
142.6 b
179.9 ab
193.2 b
177.6 ab
160.1 a
151.6 a
179.3 a
191.5 ab
210.0 b
2.7 a
3.1 ab
2.9 ab
2.9 ab
4.8 c
3.9 bc
2.5 ab
2.5 ab
2.7 b
2.1 a
2.8 b
1.9 a
1.7 a
2.6 b
25.3 b
27.3 b
27.3 b
26.9 b
16.0 a
27.6 b
28.7 ab
26.9 ab
30.4 b
26.1 a
25.5 a
24.7 a
24.9 a
24.8 a
2004
99.1 b
100 b
100 b
100 b
45.4 a
99.8 b
96.1 ab
99.1 b
100 b
99.3 b
91.1 a
97.0 a
98.4 a
99.8 a
Amount of
fruits with
blush over
>50% of
skin
Vaisiø,
nusispalvinusiø >50%,
kiekis, %
91.3 b
92.8 b
90.6 b
95.4 b
21.9 a
87.3 b
63.6 a
86.8 a
68.3 a
85.8 a
80.4 a
40.2 a
38.1 a
69.2 a
* – standard trees / standartiniai medþiai
Averages followed by the same letter do not differ significantly at P=0.05 (Duncan’s multiple
range test) / Tarp ta paèia raide paþymëtø vidurkiø pagal Dunkano kriterijø (p=0,05) esminio
skirtumo nëra.
K – stoolbeds established from in vitro propagated mother plants / augynai, suformuoti ið
in vitro dauginamø motininiø augalø
A – adult subclone / subrendæs subklonas
J – juvenile subclone / juvenalinis subklonas
Results and discussion. T r e e h e a l t h. During ten-year-long period of
tree growth there was no loss of trees due to frost damage to the cultivar or root
system. The highest number of trees of the cultivar ‘Ligol’ were lost due to them
falling over during periods of strong winds while carrying a heavy crop. Out of 12
trees planted, the following numbers were lost: on P 22/J – 3 trees, on M.9 RN 29 –
3 trees, on P 22/K – 2 trees, on M.9 EMLA – 2 trees, on P 59 2 trees and on P 60
– 2 trees. These results show that strongly dwarfing rootstocks such as P 22 and its
subclones, and P 59 and some subclones of M.9 had poorly developed root systems.
The poor rooting ability of trees growing on very dwarfing rootstocks corresponds
with the observations made by Webster (1999), Webster and Hollands (1999), and
Wertheim (1998). Six of 16 lost trees of the cultivar ‘Ligol’ had on-stem infection
175
with Nectria canker. The bark and wood of ‘Ligol’ trees is more sensitive to this
disease than those of ‘Jonagold’ trees. The higher yield efficiency index of the cultivar
‘Ligol’ was also more favourable to the trees falling over because of a heavy fruit
crop. Much smaller number of ‘Jonagold’ trees were lost (accidentally only 5).
T a b l e 2. Trunk cross-sectional area, yield, yield efficiency and
quality of fruits of cv. ‘Ligol’ grown on subclones of M.9
and P 22, and some Polish-bred rootstocks
2
l e n t e l ë. ‘Ligol’ veislës obelø su M.9 ir P 22 subklonais ir kai kuriais
lenkiðkos kilmës poskiepiais kamieno skerspjûvio plotas, derlius,
produktyvumas ir vaisiø kokybë
Rootstocks
Number
of lost
trees
from 12
plants
Poskiepiai
Þuvusiø
medþiø
skaièius iš
12
sodinukø
P 22*
P 22/K
P 22/A
P 22/J
P 59
M.9 EMLA*
M.9 T337
M.9 Pajam 1
M.9 RN 29
M.26*
P 14
P 60
0
2
0
3
2
2
0
1
3
1
0
2
TCSA in
2004
(cm2)
Total
yield,
1996–
2004
(kg/tree)
KSP 2004
m., cm2
Suminis
derlius
1996–
2004 m.,
kg/medis
42.9 bc
44.7 c
40.7 c
33.4 b
12.2 a
55.8 a
55.1 a
54.9 a
61.1 a
76.6 b
85.1 b
60.1 a
138.6 b
153.3 b
156.8 b
137.5 b
75.8 a
191.2 a
203.0 a
179.9 a
193.5 a
197.6 a
210.1 a
191.1 a
Amount of Amount of
fruits with fruits with
Yield
Weight
of
diameter blush over
efficiency
>50% of
2
100
fruits
>7 cm
(kg/cm
skin
100 vaisiø
Vaisiø,
kuriø
TCSA)
Vaisiø,
skersmuo
masë, kg
Produktyvu
nusispalvinu>7 cm,
mas, kg/cm2
siø >50%,
kiekis, %
KSP
kiekis, %
3.5 a
3.5 a
4.0 a
4.2 a
6.4 b
3.5 a
3.8 a
3.3 a
3.3 a
2.6 a
2.8 a
3.2 a
22.5 a
30.4 b
21.7 a
23.1 ab
25.9 ab
30.5 a
26.9 a
26.9 a
27.2 a
27.4 a
31.5 a
24.2 a
2004
96.2 a
97.5 a
92.8 a
91.6 a
93.5 a
91.9 a
97.2 ab
100 b
100 b
91.5 a
93.5 a
88.9 a
96.1 a
84.8 a
88.3 a
97.9 a
97.2 a
79.2 a
86.8 a
100 a
92.2 a
87.3 a
95.7 a
94.3 a
* – standard trees / standartiniai medþiai
Explanation see in Table 1 / Paaiðkinimus þr. 1 lentelëje
T r e e v i g o u r. After ten years, the least vigorous growth was shown by
those trees of both cultivars that were growing on P 59 and P 61. Trees growing on
the subclones of P 22 were similar in size to the trees growing on the standard
rootstock P 22. However, ‘Jonagold’ trees on P 22/A were the biggest, and ‘Ligol’
trees on P 22/J were the smallest when compared with the trees growing on the
traditionally propagated P 22. After seven years the relation between the size of tenyear old trees on the subclones of P 22 was almost the same as that previously noted
by Czynczyk et al. (2004). The trees of ‘Jonagold’ on P 61 were significantly smaller
than the trees growing on the traditionally propagated rootstock P 22. Within the
group of the standard dwarfing rootstocks, ‘Jonagold’ and ‘Ligol’ trees on the
subclones of M.9 were similar in size. The most vigorously growing trees were
obtained on the M.9T 337 subclone, whereas the smallest trees of ‘Jonagold’ were
176
obtained on the newly bred P 62 rootstock – they were significantly smaller than the
trees grown on M.9 EMLA. Small differences found in the group of the M.9 subclones
are in line with the reports by Kurlus and Ugolik (1999), Engel (1999) and Sadowski
et al. (2004). Within the group of semi-dwarf trees, both ‘Jonagold’ and ‘Ligol’ trees
grew more vigorously on P 14 in comparison with the trees on M.26. The trees on
P 60 of both cultivars were significantly smaller than the trees growing on M.26 –
the standard rootstock. The obtained results relating to the vigour of dwarf and
semi-dwarf trees correspond with the results presented by Bielicki et al. (1999),
Czynczyk et al. (2004), Czynczyk and Bartosiewicz (2003), and Jadczuk (2000).
Y i e l d. All the trees of two apple cultivars began bearing fruit in the second
year after planting. Yield per tree in the following years corresponded to the size of
the tree. Higher yields were usually obtained from larger trees. After ten years, within
the group of the least vigorously growing trees, the total yields for both cultivars on
the subclones of P 22 were similar in size to the total yields obtained from the control
trees on P 22. The lowest total yield was obtained from the smallest trees on P 59.
A lower yield for ‘Jonagold’, in comparison with the yield from all the trees on the
subclones of P 22, was also obtained from the trees growing on the new P 61
rootstock. In the group of dwarf trees, the total yields for both cultivars were similar
in size to the total yields obtained from the standard trees growing on M.9 EMLA.
The obtained results relating to the total yield of ‘Jonagold’ and ‘Ligol’ cultivars
growing on the dwarfing rootstocks followed a trend similar to those presented
earlier by Jakubowski (1999), Bielicki et al. (1999) and Czynczyk et al. (2004).
Within the group of semi-dwarf trees, the total yields for both cultivars were similar
in size to the cumulative yields obtained from trees on M.26, with the exception of
the yields obtained for ‘Jonagold’ trees on P 60. The cumulative yield for ‘Jonagold’
trees on P 60 was significantly higher in comparison with the yield obtained from
trees on M.26. Yield data related to the rootstocks in this experiment correspond
with those presented previously by Bielicki et al. (1999) and Czynczyk et al. (2004).
The total yield efficiencies (in kg per cm2 of trunk cross-sectional area) within the
group of trees growing on the subclones of P 22 were higher than the yield efficiencies
obtained from standard trees on P 22. ‘Jonagold’ and ‘Ligol’ trees on P 59 had
significantly higher yield efficiency index. ‘Jonagold’ trees growing on P 61 also had
higher yield efficiency index than the standard trees on P 22. Within the group of
dwarf trees on M.9 EMLA and its subclones, the numerical values of the yield
efficiency index were very similar. Similar values of the yield efficiency index had
also ‘Jonagold’ trees on the new P 62 rootstock. In the group of semi-dwarf trees of
both cultivars, the highest yield efficiency index was obtained for trees on the P 60
rootstock. The results concerning the yield efficiency index for the different rootstocks
are in agreement with the data presented earlier by Czynczyk and Bartosiewicz (2003),
Czynczyk and Bielicki (2002) and Czynczyk et al. (2004). The size and weight of
fruits of both cultivars were similar for all the rootstocks with the exception of
‘Jonagold’ trees on P 59. In 2004, ‘Jonagold’ trees on this rootstock produced
significantly smaller fruits. Fruitlets on ‘Jonagold’ trees growing on P 59 have to be
thinned more carefully. In 2004, ‘Jonagold’ apples obtained from trees on P 59 also
177
had the smallest red blush on their surface. Winter and summer pruning of ‘Jonagold’
trees on P 59 have to be done very carefully.
Conclusions. 1. The subclones P 22/A and P 22/J showed growth vigour very
similar to P 22 (standard). The P 22/K rootstock obtained from stoolbeds established
from in vitro propagated mother plants contributed to the growth vigour of ‘Jonagold’
trees similar to that of the trees growing on P 22 (standard). Trees on the new
rootstock P 61 were also similar in size to the trees on P 22 (standard). The smallest
trees of both cultivars were obtained on P 59.
2. Growth vigour of subclones of M.9 rootstock (M.9 T 337, M.9 Pajam 1 and
M.9 RN 29) was similar to the standard M.9 EMLA. However, both cultivars on the
M.9 Pajam 1 subclone showed the weakest growth. Trees of the cultivar ‘Jonagold’
on the new rootstock P 62 were significantly smaller than the trees on M.9 EMLA
and all the other subclones of M.9.
3. Within the group of semi-dwarf trees, both ‘Jonagold’ and ‘Ligol’ trees grew
less vigorously on P 60 and more vigorously on P 14 in comparison with the trees on
M.26.
4. The total yields obtained from trees growing on the subclones of M.9 and
P 22 were similar to the total yields from trees growing on M.9 EMLA and P 22 – the
standard rootstocks. ‘Jonagold’ trees growing on the semi-dwarfing rootstocks
P 14 and P 60 produced higher total yields than trees on the standard rootstock
M.26. The highest yield efficiency within the group of the very dwarfing rootstocks
was achieved by trees on P 59 followed by those on P 61, whereas among the
subclones of M.9 the most efficient were ‘Jonagold’ trees on M.9 Pajam 1.
5. Tested subclones of M.9 and P 22, and new rootstocks with varying vigour
produced no significant effect on the size, weight or colouring of apples, with the
exception of ‘Jonagold’ trees growing on P 59. More attention has to be paid to very
careful winter and summer pruning and the thinning of fruitlets when growing
‘Jonagold’ on P 59.
Gauta
2006 05 23
Parengta spausdinti
2006 07 13
References
1. B i e l i c k i P., C z y n c z y k A. and B a r t o s i e w i c z B. Effects of
new polish rootstocks and some M.9 clones on growth cropping and fruit quality of three
apple cultivars. Proceedings of the International Seminar “Apple Rootstocks for intensive
Orchards” (Warsaw-Ursynów, Poland, 18-21 08 1999). 1999. P. 15-16.
2. C z y n c z y k A. New apple rootstocks from the Polish breeding program
International Dwarf Fruit Tree Association, Pennsylvania. Compact Fruit Tree. 1995. Vol.
28. P. 68-76.
3. C z y n c z y k A. The growth and fruiting of two apple cultivars replanted over
the old apple orchard at various densities. J. Fruit Ornam. Plant Res. 2000. (1). P. 19-24.
178
4. C z y n c z y k A. and P i s k o r E. Effect of P 22 rootstocks propagated ‘in
vitro’ and traditionally on growth and fruiting of two apple cultivars. Folia Hort. 2000.
12/1. P. 29-39.
5. C z y n c z y k A., B a r t o s i e w i c z B. Results of a nine-year study of the
effect of semigrowing rootstocks on the growth and yielding of the ‘Ligol’ apple. Folia
Hort. Ann. 2003. 15/1, 2003. P. 49-56.
6. C z y n c z y k A., B i e l i c k i P. Ten-year results of growing the apple
cultivar ‘Ligol’ in Poland. Hort. Veget. Grow. 2002. 21(4). P. 12-21.
7. C z y n c z y k A., B i e l i c k i P., B a r t o s i e w i c z B. Testing New
Dwarfing Apple Rootstocks from Polish and Foreign Breeding Programmes. Acta Hort.
2001. 557. P. 83-89.
8. C z y n c z y k A., B i e l i c k i P., B a r t o s i e w i c z B. Influence of
subclones of M.9 and P 22 and new Polish-bred rootstocks on growth and yields of
‘Jonagold’ and ‘Ligol’ apple trees. Acta Hort. 2004. 658. P. 129-133.
9. E n g e l A. Effect of different M.9 subclones and M.9 cross-breed rootstocks
on growth, yield and fruit quality of three apple cultivars. Proceedings of the International
Seminar “Apple Rootstocks for intensive Orchards” (Warsaw-Ursynów, Poland, 18–21 08
1999). 1999. P. 25-26.
10. J a d c z u k E. Growth and bearing of ‘Jonagold’ apple trees on eight rootstocks.
Acta Hort. 2000. 517. 175 p.
11. J a k u b o w s k i T. Preliminary evaluation of new rootstocks clones. Proc. of
the Eucarpia. Symp. of Fruit Breeding and Genetics. Acta Hort. 1999. 484. P. 97-100.
12. K u r l u s R. and U g o l i k M. Effect of 13 rootstocks on growth and yielding
of ‘Sampion’ apple trees. Proc. Int. Seminar “Apple Rootstocks for Intensive Orchards”
(Warsaw-Ursynów, Poland, 18–21 08 1999). 1999. P. 65-66.
13. L i s t of cultivars of fruit trees and berry plants. Res. Center for Cultivar Testing.
S³upia Wielka, Poland, 1997.
14. M i k a A. Nowoczesny sad karowy. Hortpress. Warszawa, 1995.
15. S a d o w s k i A., D z i u b a n R. and J a b ù o ñ s k i K. Growth and
Cropping of Three Apple Cultivars on Different Rootstocks over a 7-year Period. Acta
Hort. 2004. 658. P. 257-263.
16. S k r z y ñ s k i J., P o n i e d z i a ù e k W. Growth and cropping of
‘Jonagold’ apple trees on six different rootstocks: M.9, M.26, P 2, P 14, P 22 and P 60.
Proceedings of the International Seminar “Apple Rootstocks for intensive Orchards”.
Warsaw-Ursynów, Poland, 1999.
17. W e b s t e r A. D. Dwarfing rootstocks for apple: past, present and future.
Proceedings of the International Seminar “Apple Rootstocks for intensive Orchards”
(Warsaw-Ursynów, Poland, 18–21 08 1999). 1999. P. 9-14.
18. W e b s t e r A. D. and H o l l a n d s M. S. Orchard comparison of ‘Cox’s
Orange Pippin’ grown on selections of the apple rootstock M.9. J. Hort. Sci.& Biotech.
1999. 74(4). P. 513-521.
19. W e r t h e i m S. J. Rootstock Guide. Fruit Research Station Wilhelminadorp
the Netherlands. The Netherlands, 1998.
20. Z a g a j a S. W., J a k u b o w s k i T., P r z y b y ù a A. P 60 a new
vegetative apple rootstock. Fruit Sci. Rep. 1991. 18(1). P. 25-30.
179
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
173–180.
‘JONAGOLD’ IR ‘LIGOL’ VEISLIØ OBELØ AUGIMAS IR DERËJIMAS SU
M.9, P 22 SUBKLONAIS IR KAI KURIAIS LENKIÐKAIS POSKIEPIAIS
A. Czynczyk, P. Bielicki, B. Bartosiewicz
Santrauka
Sode 10 metø buvo tirta M.9 subklonø: M.9T 337, Pajam 1, RN 29, P 22 subklonø:
P 22/K, P 22/A, P 22/J, ir kai kuriø naujø lenkiðkø poskiepiø (P 59, P 60, P 61 ir P 62) átaka
‘Jonagold’ ir ‘Ligol’ veisliø obelø augimui ir derëjimui. Abiejø veisliø vaismedþiø su M.9
subklonais augumas buvo labai artimas augumui su standartiniu poskiepiu M.9 EMLA,
bet vaismedþiai su Pajam 1 buvo maþiausi. ‘Jonagold’ vaismedþiai su nauju lenkiðku P 62
poskiepiu augo daug lëèiau negu su M.9 EMLA. Abiejø veisliø vaismedþiø augumas su
P 22 subklonais buvo panaðus kaip su standartiniu poskiepiu P 22. ‘Jonagold’ vaismedþiai
su P 61 poskiepiu buvo ið esmës þemesni uþ vaismedþius su P 22. Maþiausi abiejø veisliø
vaismedþiai buvo su P 59 poskiepiu. Pusiau þemaûgiø poskiepiø grupëje þemiausi
vaismedþiai buvo su P 60, didþiausi – su P 14 poskiepiu. Derlius buvo beveik proporcingas
vaismedþio dydþiui. Ið P 22 subklonø didþiausi abiejø veisliø derliai gauti su P 22/A, ið M.9
subklonø – su M.9T 337, pusiau þemaûgiø ‘Jonagold’ vaismedþiø grupëje – su P 60,
‘Ligol’ – su P 14. M.9 subklonø produktyvumas buvo panaðus á M.9 EMLA, o ið P 22
subklonø ðio rodiklio reikðmës buvo panaðios á standartinio P 22 poskiepio. Ið pusiau
þemaûgiø poskiepiø produktyviausi buvo vaismedþiai su P 60. 2004 metais abiejø veisliø
su dauguma tirtø poskiepiø vaisiø kokybës rodikliai (dydis, masë ir vaisiø, kuriø þievë
paraudusi daugiau kaip 50%, procentas) nesiskyrë. Kur kas maþesni ‘Jonagold’ obuoliai
iðaugo tik su P 59.
Reikðminiai þodþiai: obelys, poskiepiai, subklonas, augimas, produktyvumas, vaisiø
kokybë.
180
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 181–191.
FIELD PERFORMANCE OF GENEVA® APPLE
ROOTSTOCKS IN THE EASTERN USA
Terence L. ROBINSON1, Gennaro FAZIO2,
Herbert S. ALDWINCKLE3, Stephen A. HOYING4, Nicole RUSSO3
1
Dept. of Hort. Sciences, New York State Agricultural Experiment Station,
Cornell University, Geneva, New York, 14456 USA.
E-mail: [email protected]
2
USDA-ARS, Geneva, New York 14456 USA. E-mail: [email protected]
Dept. of Plant Pathology, New York State Agricultural Experiment Station,
Cornell University, Geneva, New York, 14456 USA.
E-mail: [email protected]
3
Cornell Cooperative Extension, 1581 Rt 88N Newark, New York, 14568
USA. E-mail: [email protected]
4
Series of replicated trials in New York State were established in 1998–2002 to evaluate
the Cornell-Geneva series of apple rootstocks which have been bred for resistance to fire
blight and Phytophthora root rot, high yield efficiency and good tree survival. Among
dwarfing rootstock candidates that are similar in size to M.9, Geneva® 41 (G.41), G.11 and
G.16 have shown the greatest yield efficiency and have equaled or exceeded the
performance of M.9. G.41 has shown a high level of resistance to fire blight and has also
shown good cold hardiness in test winters, while G.11 has shown a moderate level of
resistance to fire blight. G.16 showed significantly greater winter survival than M.9, M.26
or B.9 in a mid-winter freeze event in 2004 but greater tree damage than M.9 from the late
fall freeze in 2003. Among semi-dwarfing rootstock candidates that are similar in size to
M.26, both G.935 and G.202 had significantly greater yield efficiency than M.26. In addition,
they both have shown high resistance to fire blight and good tolerance to apple replant
disease. Both have shown good winter survival to midwinter cold events.
Key words: Malus X domestica, fire blight, yield efficiency, dwarfing, winter hardiness,
graft union strength, anchorage.
Introduction. The adoption of high-density apple orchards on dwarfing
rootstocks has allowed apple growers to achieve earlier production, higher production
and better fruit quality than previously. However, for many apple growers in North
America, New Zealand and some locations in Europe, the bacterial disease fire blight
is a serious threat to dwarf apple orchards (Norelli et al., 2003). M.9 and M.26, the
most common dwarfing apple rootstocks, are very susceptible to this disease and in
some locations this disease limits the planting of dwarfing rootstocks. Outbreaks of
the disease in the eastern USA have decimated many dwarf apple orchards.
181
In 1970, Dr. James Cummins and Dr. Herbert Aldwinckle initiated an apple
rootstock breeding project at the Cornell University, Geneva, NY, with the objective
of developing rootstock genotypes with improved nursery and orchard characteristics
that were better adapted to the biotic stresses of fire blight (Erwinia amylovora),
and crown rot (Phytophthora spp.) which are common in New York State and
surrounding areas (Cummins and Aldwinckle, 1983). Progeny from planned crosses
underwent rigorous greenhouse screening procedures at the small seedling stage to
select for tolerance to fire blight and crown rot. Surviving genotypes were then
tested for propagation characteristics in the nursery, and productivity and dwarfing
at the New York State Agricultural Experiment Station in Geneva, New York. Since
1991, the elite selections from the breeding program have been tested in field trials at
various locations around the world (USA: Robinson et al., 2003; Robinson and Hoying,
2004; Robinson et al., 2004; France: Masseron and Simard, 2002 and New Zealand:
personal communication from Stuart Tustin). In this paper, we report on the
performance of Geneva® rootstocks from a series of trials in two apple growing
regions of New York State planted from 1998–2002 where we assessed survival,
precocity, productivity, fruit size and field tolerance to fire blight.
Materials and Methods. In 1998, 1999, 2001 and 2002, rootstock trials were
planted in two apple-growing regions of New York State (Lake Ontario and Lake
Champlain regions) (Table 1). Each trial had 1-9 Geneva® rootstock clones with
appropriate Malling rootstock controls. In the 1998 trial two sources or rootstock
liners were compared. The first group came from stoolbed mother plants, which
had been propagated by stoolbed layering. The second group came from stoolbed
mother plants, which had been propagated by tissue culture.
T a b l e 1. Replicated Geneva® rootstock trials planted in New York
State
1
l e n t e l ë. Niujorko valstijoje árengti Geneva® poskiepiø bandymai
Farm name
Ûkio
pavadinimas
Geneva
Peters
Chazy
Geneva
Region of New Year of
planting
York State
Niujorko valstijos Sodinimo
regionas
metai
Variety
Veislë
Lake Ontario
1998 ‘Jonagold’
Lake Ontario
1999 ‘McIntosh’
Ontarijo ežeras
Ontarijo ežeras
Lake Champlain
Èempleino ežeras
Lake Ontario
Ontarijo ežeras
Rootstocks in trial
Tiriami poskiepiai
G.41, G.16, M.9
G.16, G.30, G.41, G202, G935,
CG.4013, CG.6210, CG.6814,
CG.7707, M.9, M.26, M.7, Supporter 1,
Supporter 2, Supporter 3, Supporter 4
2001 ‘McIntosh’, G.16, G.30, Ottawa 3, Vineland 3,
‘Honeycrisp’ Vineland 1, Mark, Bud.118, Bud.9,
M.9T337, M.9Nic29, M.26, M.111,
M.7, MM.106, Supporter4
2002 ‘Gala’,
G.11, G.16, G.41, G.65, G.935, JM.2,
‘Honeycrisp’ JM.7, M.9T337, M.9EMLA, M.9Nic29,
M.9Burg756, M.26EMLA,
M.26NAKB, M.27, Ottawa 3, P.14,
P.22, PiAu56-83, Supporter 4
182
All of the trees for each experiment were grown in a common nursery in Geneva,
NY. At planting, the trees, which were unbranched whips, were headed at 90 cm.
Each experiment was laid out as a randomized complete block with 4–8 replications.
All of the experiments utilized single tree plots. Trees were supported and trained to
the Vertical Axis system. The plots were managed with standard New York State,
fertilization, ground cover management and chemical fruit thinning programs. Annual
yield, fruit size, tree size (trunk circumference measured at 30 cm above the graft
union) and survival data were collected. The plot planted in the Champlain region in
2001 experienced considerable winter tree death in January of 2004. The damage
occurred to the roots and rootstock shank and not to the scion or scion buds. The
damage resulted from the combination of excessive moisture in December, followed
by a warm period in early January and then a sudden drop in temperature to –32°C.
Low temperatures remained at that level each night for several weeks. Tree mortality
was recorded in the spring of 2004.
In the 2002 plot we inoculated each of the scions during bloom with fire blight
in 2005. We then recorded rootstock death at the end of the season. All data were
analyzed by ANOVA and mean comparison was done with LSD, P≤0.05.
Results. Geneva rootstocks, which have been named and released in the USA,
include G.11, G.16, G.30, G.41, G.65, G.202 and G.935. Other unreleased numbered
selections are designated as CG stocks. In the 1998 plots, ‘Gala’/ G.16 trees were
13% larger in size but not significantly different than trees on M.9EMLA at the end
of 8 years in the orchard, but the ‘Jonagold’/ G.16 trees were 7% smaller in size but
not significantly different than the trees on M.9EMLA (Table 2). With ‘Jonagold’,
T a b l e 2. Tree size and yield of ‘Jonagold’ on G.16 and G.41
rootstocks and ‘Gala’ on G.16 after 8 years at Geneva, New
York (planted in 1998)
2
Variety
Veislë
l e n t e l ë. ‘Jonagold’ veislës vaismedþiø su G.16 ir G.41 poskiepiais ir ‘Gala’
veislës su G.16 poskiepiu dydis ir 8 metø derlius. Þeneva, Niujorko
valstija (pasodinta 1998 m.)
Rootstock*
Tree
survival
Kamieno
skerspjûvio plotas,
Suminis
derlius,
% M.9E
% M.9E
% M.9E
100
100
100
100
100
G.16
93
133
94
89
100
G.41
83
166
116
91
100
LSd05/R05
19
33
16
5
G.16
113
112
99
91
100
M.9T337
78
121
143
95
100
M.9EMLA
100
100
100
100
100
LSd05/R05
27
25
27
6
Poskiepis
‘Jonagold’ M.9EMLA
‘Gala’
Trunk cross- Cumulative Cumulative yield Average fruit
sectional area
yield
efficiency
size
Produktyvumas,
Vidutinis vaisiaus Vaismedþiø
dydis, % M.9E išlikimas, %
* Rootstocks ranked by trunk cross-sectional area / Poskiepiai sugrupuoti pagal kamieno
skerspjûvio plotà.
183
tree size of G.41 was significantly smaller (18%) than M.9EMLA. Cumulative yield
of ‘Gala’/ G.16 trees was also not significantly higher than trees on M.9EMLA resulting
in similar yield efficiency as trees on M.9EMLA (Table 2). With ‘ Jonagold’, both
G.16 and G.41 had significantly higher yield than M.9EMLA. The ‘Jonagold’/G.41
trees had significantly higher yield efficiency than trees on M.9EMLA. With G.16
yield efficiency was not significantly different than trees on M.9EMLA. Fruit size of
both G.16 and G.41 was significantly smaller than M.9EMLA. In the case of G.41
this was the result of greater crop load while with G.16 fruit size was smaller despite
having similar crop load as M.9.
The comparison of the effect of tissue culturing of the stoolbed mother plants
on orchard performance of rootstocks showed no significant differences in tree
size, yield, yield efficiency or root suckers of ‘Jonagold’ trees on G.16 rootstock
when the rootstock liners came from stoolbeds where the mother plants were from
tissue cultured plants compared to trees on G.16 when the liners came from non
tissue cultured mother plants (Table 3).
T a b l e 3. Effects of tissue culture propagation on the performance
of G.16 rootstock after 8 years with ‘Jonagold’ as the scion
at Geneva, New York State (planted in 1998)
3
l e n t e l ë.
Rootstock*
Poskiepis
Audiniø kultûroje padauginto G.16 poskiepio átaka ‘Jonagold’
veislës obelø augimui ir derëjimui 8 metus. Þeneva, Niujorko
valstija (pasodinta 1998 m.)
Trunk crosssectional area
Kamieno
skerspjûvio plotas,
cm2
Average
fruit size
Root
suckers
(no./tree)
Cumulative
yield (kg/tree)
Cumulative yield
efficiency
Suminis derlius,
kg/medis
Produktyvumas,
2
Vidutinë
vaisiaus
masë, g
Ðaknø atþalos,
vnt./ vaism.
kg/cm KSP
G.16 non TC
40.4
133
3.4
240
0.3
G.16 TC**
LSd05/R05
43.9
9.2
135
24
3.1
0.8
234
14
0.3
0.3
* Rootstocks ranked by trunk cross-sectional area / Poskiepiai sugrupuoti pagal kamieno
skerspjûvio plotà.
**TC= Liners derived from tissue cultured stoolbed plants / Poskiepiai iðauginti ið audiniø
kultûroje padaugintø motininiø augalø.
In the 1999 dwarf rootstock plot with ‘McIntosh’, the smallest trees were on
G.16, M.9 and Supporter 1 (Table 4). Intermediate in size between M.9 and M.26
were G.41 and Supporter 3. Similar to M.26 in size were G.202 and G.935. The
highest cumulative yield was with G.935 followed by G.41, G.202, Supporter 3,
Supporter 2, G.16, M.9 and lowest with Supporter 1. The highest yield efficiency
was with G.41 followed by G.935, G.16, Supporter 2, M.9, Supporter 3, Supporter
1, M.26 and lowest with G.202. Fruit size was largest with G.41 followed by M.26,
G.935, G.202, M.9, Supporter 2, Supporter 1, Supporter 3, and smallest with G.16.
The greatest number of root suckers was with M.9 while all of the other stocks did
not differ from zero. Tree survival was lowest with M.9 and significantly lower than
all of the other stocks, which were not different than 100%.
184
T a b l e 4. Seven-year performance of ‘McIntosh’ on several dwarf
rootstocks in New York State (planted in 1999)
4
l e n t e l ë. ‘McIntosh’ veislës obelø su keliais þemaûgiais poskiepiais augimas ir
derëjimas septynerius metus Niujorko valstijoje (pasodinta 1999 m.)
Trunk crossCumulative Average Number of
Cumulative
Tree survival
area
size
Rootstock* sectional
yield
efficiency fruit
yield (kg/tree)
Kamieno
Vidutinë root suckers Vaismedþiø
Produktyvumas,
Poskiepis
vaisiaus Ðaknø atþalø išlikimas, %
skerspjûvio Suminis derlius,
kg/vaism.
skaièius
2
kg/cm2 KSP
plotas, cm
masë, g
G.16
39.3
90.0
2.30
166
0.0
100
M.9T337
39.6
79.8
2.04
178
6.7
50
Supporter1
42.2
75.3
1.77
172
2.3
100
G.16TC**
43.3
72.3
1.66
167
1.0
100
Supporter2
44.8
101.0
2.22
174
0.2
100
G.41
48.8
119.0
2.37
192
0.0
83
Supporter3
50.3
101.0
2.02
170
0.0
83
M.26EMLA
64.5
98.1
1.56
183
0.0
100
G.202
73.3
111.0
1.46
180
1.7
100
G.935
79.0
183.0
2.31
181
2.3
100
LSd05/R05
14.9
33.8
0.42
13
3.3
28
* Rootstocks ranked by trunk cross-sectional area / Poskiepiai sugrupuoti pagal kamieno
skerspjûvio plotà.
**TC= Liners derived from tissue cultured stoolbed plants / Poskiepiai iðauginti ið audiniø
kultûroje padaugintø motininiø augalø.
In the 1999 semi-dwarf rootstock plot with ‘McIntosh’, the smallest trees were
on M.26 and G.6210 (Table 5). G.30 was intermediate in size between M.26 and
M.7 while Supporter 4 was similar in size to M.7. The highest cumulative yield was
with G.30 followed by M.7, Supporter 4, G.6210, and lowest with M.26. The highest
yield efficiency was with G.6210 and G.30 followed by M.26, M.7 and lowest with
Supporter 4. Fruit size was largest with G.6210 followed by M.7, G.30, G.6210,
and smallest with Supporter 4. The greatest number of root suckers was with M.7,
which had significantly greater number of suckers than G.30, which was followed
by Supporter 4, G.6210 and M.26, which did not differ from zero. Tree survival
was the lowest with G.30 but was not significantly different than 100%.
Rootstock had a significant effect on tree survival following the mid-winter
cold snap of 2004 in the 2001 plot in the Champlain region of New York State. With
‘Honeycrisp’ and ‘McIntosh’ as the scions, ‘Ottawa 3’, ‘Vineland 1’ ‘Vineland 3’,
G.16, G.30 and ‘Mark’ had the greatest survival followed by B.118, M.9T337, B.9,
M.9Nic29 and Supporter 4 (Table 6). M.26, MM.111, M.7 and MM.106 had very
poor survival.
In the 2002 plot, inoculation with fire blight caused significant scion infection
on all trees and with susceptible rootstocks significant tree death. The greatest tree
death was with M.9 and M.26 (Table 7). An intermediate amount of tree death was
observed with M.27. A low level of tree death was observed with G.11, G.65 and
185
G.935. No tree death was observed with G.16 and G.41.
T a b l e 5. Seven-year performance of ‘McIntosh’ on several semidwarf rootstocks in New York State (planted in 1999)
5
l e n t e l ë. ‘McIntosh’ veislës obelø su keliais pusiau þemaûgiais poskiepiais
augimas ir derëjimas septynerius metus Niujorko valstijoje
(pasodinta 1999 m.)
Trunk cross- Cumulative Cumulative
yield
sectional area
yield
Rootstock*
(kg/tree)
efficiency
Kamieno
Poskiepis
skerspjûvio
2
plotas, cm
Suminis
derlius
kg/medis
M.26EMLA
49.0
CG.6210
Average
fruit size
Vidutinë
Produktyvumas vaisiaus masë,
Number of Tree survival
root suckers
Vaismedþiø
Šaknø atþalø
išlikimas, %
skaièius
kg/cm2 KSP
g
57.2
1.19
188
0.7
100
56.8
75.1
1.30
174
1.8
100
G.30TC**
75.2
77.8
1.01
184
6.6
80
G.30
82.4
107.0
1.29
175
7.0
100
Supporter 4
106.5
93.9
0.93
170
3.7
100
M.7EMLA
107.0
104.0
1.03
186
33.0
100
LSd05/R05
24.4
31.4
0.44
18
16.0
32
*Rootstocks ranked by trunk cross-sectional area / Poskiepiai sugrupuoti pagal kamieno
skerspjûvio plotà.
**TC= Liners derived from tissue cultured stoolbed plants / Poskiepiai iðauginti ið audiniø
kultûroje padaugintø motininiø augalø.
Discussion. Our data have shown that over a broad range of climates and soils,
that 3 Geneva® stocks, G.11, G.41 and G.16, are very similar in dwarfing to M.9.
Geneva® 11, which is a 1978 cross of ‘Malling 26’ X ‘Robusta 5’ was released in
1999. Our earlier data showed it to be similar in size and yield efficiency to M.26
(Robinson et al., 2003). However, in those trials M.26 grew poorly. Our more recent
data shows G.11 to be similar in size to M.9. Similar results were found in France
(Masseron and Simard, 2002). Our current data shows that G.11 is fire blight resistant
but is not immune. This confirms our earlier data (Norelli et al., 2002). It also has
good resistance to Phytophthora root rot, but it is not resistant to woolly apple
aphids or apple replant disease (Isutsa and Merwin, 2000). G.11 has good layerbed
and nursery characteristics. It may prove to be an excellent replacement for M.9.
Geneva® 16, which is a 1981 cross of ‘Ottawa 3’ X Malus floribunda, was
released in 1998. Our data show it to be similar in vigor to vigorous clones of M.9
(i.e. Nic29 or Pajam2). G.16 is a good rooter in the stoolbed and produces a large
tree in the nursery. Tree growth in the first 2 years in the orchard is vigorous, but
with the onset of cropping, tree vigor is moderated giving a final tree size similar in
size to M.9. G.16 appears to have wide soil adaptability and some tolerance to replant
disease (unpublished data). G.16 showed similar precocity and cumulative yield
efficiency as M.9. G.16 also exhibited very good mid-winter hardiness having survived
186
T a b l e 6. Survival of three-year-old ‘Honeycrisp’ and ‘McIntosh’
apple trees on several rootstocks following the severe
winter weather of 2004 in the Champlain region of New
York State (planted in 2001)
6
l e n t e l ë. Trejø metø ‘Honeycrisp’ ir ‘McIntosh’ veisliø obelø su keliais
poskiepiais iðlikimas po 2004 metø ðaltos þiemos Niujorko valstijos
Èempleino regione (pasodinta 2001 m.)
Rootstock*
Poskiepis
Ottawa 3
Vineland 3
Vineland 1
G.16
G.30
Mark
Bud.118
M.9T337
Bud.9
M.9Nic29
Supporter 4
M.26
MM.111
M.7
MM.106
LSd05/R05
Tree survival / Iðlikusiø vaismedþiø kiekis, %
‘Honeycrisp’
‘McIntosh’
100 a
–
98 ab
–
98 ab
–
92 ab
92 a
92 ab
100 a
92 ab
96 a
88 abc
88 abc
86 abcd
36 cd
66 bcde
37 cd
55 cdef
58 bc
54 cde
–
39 ef
26 cd
36 ef
34 cd
24 fg
31 cd
0g
17 d
33
33
*Rootstocks ranked by survival with ‘Honeycrisp’ / Poskiepiai sugrupuoti pagal ‘Honeycrisp’
iðlikimà.
the 2004 winter freeze event in Northern NY that killed many M.9, B.9 and M.26
trees. However, G.16 does appear to have some susceptibility to very early winter
freeze events in the nursery (Roger Adams, personal communication). This is likely
due to its vigorous growth characteristics in the nursery and in the orchard during
the first few years where it grows late. The field inoculation trial reported here
shows it to be essentially immune to fire blight, which confirms our earlier data
(Norelli et al., 2002). It is highly resistant to Phytophthora, but it is not resistant to
woolly apple aphids. The greatest known deficiency of G.16 is its sensitivity to one
or more latent viruses in scion wood (Johnson et al., 2001). Infected scion wood
results in death of the trees in the nursery or the first year in the orchard. This
requires absolute use of virus free scion wood. A few trees have snapped off at the
graft union during high winds in one commercial orchard indicating that it has a
brittle union similar to M.9. The comparison of G.16 liners derived from tissue
cultured stoolbed mother plants versus liners derived from conventionally propagated
mother plants showed no significant differences in performance with ‘Jonagold’ as
the scion. With G.16, at least we see no negative effects of rapid plant multiplication
by tissue culture to obtain stoolbed mother plants. The liners derived from those
stoolbed mother plants appear to behave similarly to liners from conventionally
187
propagated stoolbeds. However, we do not recommend the use of tissue-cultured
plants directly as rootstock liners due to increased tree vigor. If virus free wood is
used, it appears that G.16 is a good alternative to M.9 in high fire blight areas.
T a b l e 7. Tree death of ‘Gala’ and ‘Honeycrisp’ apple trees on
various rootstocks after inoculation of the scion with fire
blight during bloom (planted in 2002)
7
l e n t e l ë.
‘Gala’ ir ‘Honeycrisp’ veisliø obelø su ávairiais poskiepiais þuvimas
vaismedþius inokuliavus bakterine deglige þydëjimo metu
(pasodinta 2002 m.)
Rootstock
Poskiepis
Tree death / Þuvusiø vaismedþiø kiekis, %
‘Gala’
‘Honeycrisp’
G.11
--
12
G.16
--
0
G.41
0
0
G.65
--
10
G.935
--
13
M.9T337
86
--
M.9EMLA
--
79
M.26EMLA
75
93
M.27
--
40
LSd05/R05
30
30
G.41, which is a 1975 cross of ‘Malling 27’ X ‘Robusta 5’, was released in
January 2005. The data show that G.41 gives a tree slightly smaller than M.9EMLA
and similar to the weak clones of M.9 such as NAKBT337 or ‘Flueren 56’. G.41 is
the most productive M.9 size rootstock in our trials. It also has excellent fruit size
and induces wide crotch angles. Our current fire blight inoculation trial shows that it
is highly resistant to fire blight and confirms our earlier data (Norelli et al., 2002). It
is also resistant to Phytophthora but it is not resistant to woolly apple aphids. It
appears to have some tolerance of apple replant disease. A comparison of performance
of stocks in an infected soil site and an uninfected soil site showed that G.41 had
similar growth in both sites while M.26 and M.9 showed significantly less growth in
the infected site (Robinson and Hoying, 2003). It survived a severe winter cold snap
in Northern NY in 1994 (Robinson and Hoying, 2003). In the stoolbed, G.41 is a shy
rooter and will require higher planting densities in the stoolbed or tissue cultured
stoolbed mother plants to improve its rooting. It also produces some side shoots in
the stoolbed. It has brittle roots and a brittle graft union similar in strength to M.9. In
one trial with ‘Gala’ as the scion, 10% of the trees broke at the graft union following
a severe windstorm. It does not have the virus sensitivity of G.16. G.41 has also
been tested in France where it was shown to be smaller in tree size than M.9Pajam2,
but more productive than M.9Pajam2, while producing similar fruit size as M.9Pajam2
(Masseron and Simard, 2002). It appears that G.41 will be a good alternative to M.9
188
in high fire blight prone areas.
Among CG stocks similar in size to M.26 rootstock, G.935, and G.202 have
performed better than M.26. G.935, which is a 1976 cross of ‘Ottawa 3’ X ‘Robusta
5’, was released in January 2005. Tree vigor of G.935 has been slightly greater than
M.26. Our data show that G.935 is the most precocious and productive semidwarf
rootstock in our trials. It has similar efficiency to M.9 along with excellent fruit size
and wide crotch angles. Our current trial with fire blight shows it is highly resistant
to fire blight and confirms our earlier data (Norelli et al., 2002). It is also resistant to
Phytophthora, appears to have some tolerance of apple replant disease, appears to
be very winter hardy, but its not resistant to woolly apple aphid. Fruit size has been
as good as M.9 and the tree has wide crotch angles. It had no winter damage during
the 1994 test winter.
Geneva® 202, which is a 1975 cross of ‘Malling 27’ X ‘Robusta 5’, was released
in 2002 in New Zealand and in 2005 in the USA. Our data show that G.202 produces
a tree slightly larger than M.26. G.202 was previously shown to have a high level of
resistance to fire blight (Norelli et al., 2002). In addition, it has good resistance to
Phytophthora, apple replant disease and to woolly apple aphid, which is an important
pest in many climates. It has had higher yield efficiency than M.26, but it has not
been as productive as G.935. In New Zealand, it has been more productive than
M.26 (Stuart Tustin, personal communication). Fruit size is similar to M.26. G.202
will be a useful alternative to M.26 in climates that have problems with woolly apple
aphid.
The resistance of the Geneva® rootstocks to fire blight is an important
characteristic in fire blight prone regions of the world. Although resistance of the
rootstock does not confer resistance to the scion, it does prevent the tree from dying
due to rootstock infections. Fire blight infections usually occur to the blossoms
during bloom and result in diseased branches that die. Once the bacteria are inside
the tree, it can travel symptomless down the trunk of the tree to the graft union and
the rootstock below. With highly susceptible rootstocks like M.9 and M.26 the
rootstock cambium, xylem and phloem at the graft union are killed causing the death
of the tree. With resistant rootstocks that are not susceptible to fire blight, the scion
can become infected, but the tree usually survived if the infected parts of the scion
were pruned away. This allows growers to prune out the infected parts of the scion
and re-grow the lost canopy quickly and restore full production much more rapidly
than replanting an entire infected dwarf orchard.
Conclusions. The results of these replicated trials have helped identify superior
CG rootstock genotypes and also helped identify the weaknesses of each stock.
G.16, G.11 and G.30 are currently being sold commercially in the USA, Canada and
Mexico. G.202 is currently being sold in New Zealand. G.41, G.202 and G.935 are
available in limited quantities in North America.
Gauta
2006 07 25
Parengta spausdinti
2006 08 04
189
References
1. C u m m i n s, J. N. and A l d w i n c k l e, H. S. 1983. Breeding apple
rootstocks, P. 294–394. In J. Janick (ed.) Plant Breeding Reviews. Westport CT, USA, AVI
Publishing.
2. I s u t s a, D. K. and M e r w i n, I. A. 2000. Malus Germplasm varies in
resistance or tolerance to apple replant disease in a mixture of New York orchard soils.
HortScience 35:262–268.
3. J o h n s o n W. C., A l d w i n c k l e, H. S., C u m m i n s, J. N.,
F o r s l i n e, P. L., H o l l e r a n, H. T., N o r e l l i, J. J. and R o b i n s o n,
T. L. 2001. The USDA-ARS/Cornell University apple rootstock breeding and evaluation
program. Acta Hort. 557:35–40.
4. M a s s e r o n, A. and S i m a r d, M. H. 2002. Les porte-greffe du pommier:
20 années d’études en France. 2e partie. Infos-Ctifl no. 175.
5. N o r e l l i, J. L., H. T. H o l l e r a n, W. C. J o h n s o n, T. L.
R o b i n s o n, and H. S. A l d w i n c k l e. 2003. Resistance of Geneva and other
apple rootstocks to Erwinia amylovora. Plant Disease. 8(1):26—32.
6. R o b i n s o n, T. L. and H o y i n g, S. A. 2004. Performance of elite CornellGeneva apple rootstocks in long-term orchard trials on growers farms. Acta Hort. 658:221–229.
7. R o b i n s o n, T, L. A n d e r s o n, A. A z a r e n k o, B. B a r r i t t,
T. B a u g h e r, G. B r o w n, G. C o u v i l l o n, W. C o w g i l l, R.
C r a s s w e l l e r, P. D o m o t o, C. E m b r e e, A. F e n n e l l, E. G a r c i a,
A. G a u s, R. G r a n g e r, G. G r e e n e, P. H i r s t, E. H o o v e r, S.
J o h n s o n, M. K u s h a d, R. M o r a n, C. M u l l i n s, S. M y e r s, R.
P e r r y, C. R o m, J. S c h u p p, K. T a y l o r, M. W a r m u n d, J.
W a r n e r, and D. W o l f e. 2003. Performance of Cornell-Geneva apple rootstocks
with ‘Liberty’ as the scion in NC-140 trials across North America. Acta Hort. 622:521–530.
8. R o b i n s o n, T., L. A n d e r s o n, A. A z a r e n k o, B. B a r r i t t,
G. B r o w n, J. C l i n e, R. C r a s s w e l l e r, P. D o m o t o, C. E m b r e e,
A. F e n n e l l, D. F e r r e e, E. G a r c i a, A. G a u s, G. G r e e n e, C.
H a m p s o n , P . H i r s t , E . H o o v e r , S . J o h n s o n , M . K u s h a d,
R. M a r i n i, R. M o r a n, C. M u l l i n s, M. P a r k e r, G. R e i g h a r d,
R. P e r r y, J. P. P r i v é, C. R o m, T. R o p e r, J. S c h u p p,
M. W a r m u n d, W. A u t i o, W. C o w g i l, K. T a y l o r, D. W o l f e.
2004. Performance Of Cornell-Geneva Rootstocks in Multi Location NC-140 Rootstock
Trials Across North America. Acta Hort. 658:241–245.
190
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
181–191.
GENEVA® OBELØ POSKIEPIØ SAVYBIØ VERTINIMAS RYTINËS JAV
DALIES SODUOSE
T. L. Robinson, G. Fazio, H. S. Aldwinckle, S. A. Hoying ir N. Russo
Santrauka
1998–2002 metais Niujorko valstijoje atlikti bandymai su obelø poskiepiais CornellGeneva, iðvestus siekiant didinti atsparumà bakterinei degligei ir ðaknø puviniui
Phytophthora, produktyvumà ir gerinti vaismedþio iðsilaikymà,. Tarp þemaûgiø poskiepiø,
kurie dydþiu panaðûs á M.9, produktyviausi buvo Geneva® 41 (G.41), G.11 ir G.16 poskiepiai,
produktyvumu pranokæ M.9. G.41 buvo itin atsparus bakterinei degligei ir iðtvermingas
þiemà, o G.11 buvo vidutiniðkai atsparus ðiai ligai. G.16 buvo iðtvermingesnis uþ M.9, M.26
ar B.9 per vidurþiemio ðalèius 2004 metais, taèiau vaismedþiai su ðiuo poskiepiu labiau
negu su M.9 nukentëjo nuo vëlyvo rudens ðalèiø 2003 metais. Tarp pusiau þemaûgiø
poskiepiø, kurie augumu panaðûs á M.26, ir G.935, ir G.202 buvo daug produktyvesni negu
M.26. Be to, jie abu buvo labai atsparûs bakterinei degligei ir gerai toleravo dirvos nuovargá.
Abu gerai iðtvërë vidurþiemio ðalèius.
Reikðminiai þodþiai: Malus X domestica, bakterinë degligë, produktyvumas,
þemaûgiai vaismedþiai, atsparumas þiemà, skiepijimo vietos tvirtumas, ásitvirtinimas.
191
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 192–198.
EFFECT OF FIVE ROOTSTOCKS ON GROWTH AND
YIELD OF FOUR APPLE CULTIVARS IN YOUNG
ORCHARD
Neeme UNIVER, Toivo UNIVER, Krista TIIRMAA
Polli Horticultural Research Centre of the Institute of Agricultural and
Environmental Sciences, Eesti Maaülikool, Estonian University of Life
Sciences; Karksi-Nuia 69104, Viljandimaa, Estonia.
E-mail: [email protected]
A trial with four cultivars ‘Talvenauding’, ‘Meelis’, ‘Alro’ and ‘Sinap Orlovskij’ grafted
on clonal rootstocks M.26, B.9, B.545, B.396 and E.75 was carried out at the Polli Horticultural
Research Centre in the spring of 2001. Fruit yield and vegetative growth were assessed
annually. Rootstocks B.9, B.396 and M.26 significantly reduced vegetative growth of
apple tree (trunk diameter and shoot length during the first four years), whereas trees on
rootstock B.545 had the strongest growth. Scion cultivars on B.9, B.396 and B.545 were
the earliest to start cropping. Trees grafted onto them started to yield in the second year
after planting. The highest cumulative yield was obtained on B.9 and B.396 followed by
M.26. The lowest yield and the smallest fruits were from trees on rootstock E.75. The
highest productivity up to 4 years after planting was obtained from the trees of ‘Sinap
Orlovskij’ on B.396 and M.26.
Key words: apple tree, clonal rootstocks, cultivars, growth, yield, fruit quality.
Introduction. All over the world, the trend in apple growing is to plant more
trees per hectare than in the past. In Estonia the intensive apple growing is still in
development stage. The establishment of intensive apple orchards has been delayed
by lack of information as well as dwarfing rootstocks suitable for Estonian conditions.
In Estonia one limited factor of rootstock selection is winter hardiness of roots.
Growth vigour, growth habit, precocity of fruit bearing, production level, fruit
size and appearance are affected by the rootstock. There were many investigations
of vigorous and semi-vigorous rootstocks in Estonia. Haak and Jalakas compared 15
different clonal rootstocks: E.19, E.20, E.26, E.28, E.37, E.39, E.53, E.56, E.63 (all
Estonian), M.11, MM.106, B.118, B.233, B.490 and A.2. All these rootstocks produced
semi-vigorous or vigorous trees (Haak, Jalakas, 2001). Another rootstock trial that
was established in 1987 performed two different studies: 1) rootstocks E20, E26,
E53, E56, E75 (all Estonian), B.233, B.490, B.545, B.118, B.396, B.9 and MM.106
were budded with four apple cultivars (‘Liivi Kuldrenett’, ‘Paide Taliõun’, ‘Tellissaare’,
192
‘Lobo’); 2) rootstocks E.37, E.39, E.63, B.257, B.476, B.491, M.7 and MM.106
were budded with cultivars ‘Tellissaare’ and ‘Lobo’. It was concluded that rootstocks
B.9, B.396, B.476, B.491 and E.75 produced dwarfing trees; less productive trees
were grown on rootstocks B.545 and E.75. The trees on the dwarfing rootstocks
yielded one third lesser than the trees on the medium rootstock MM.106 (Haak,
2003).
The aim of the present study was to compare the effect of dwarfing rootstocks
(M.26, E.75, B.9, B.545 and B.396) on tree growth and fruiting in the case of apple
cultivars ‘Alro’, ‘Cortland’, ‘Meelis’, ‘Sinap Orlovskij’ and ‘Talvenauding’.
Materials and methods. The experiment was established at the Polli Horticultural
Research Centre in South Estonia. The orchard is located on a medium loamy clay
soil with pH 5.6, containing 1.6% of organic mater, the level of P2O5 is 140 mg/kg
and K2O is 200 mg/kg. The depth of humus horizon is 20–25 cm. One-year-old
whips were planted in the spring of 2001. The spacings were 4 × 2 m (1250 tree/
ha). Apple cultivars ‘Alro’, ‘Cortland’, ‘Meelis’, ‘Sinap Orlovskij’ and ‘Talvenauding’
were tested on rootstocks B.9, B3.96, B.545, M.26 and E75. Cultivar ‘Cortland’
leaved out from trial in 2004, because apple trees in some variants perished for
various reasons. The trial design was in randomised blocks, in 5 replications and 4
trees per plot. Apple tree canopies were formed as spindle, pruned slightly, and
shoots were bent down using weights made of concrete. Along the rows weeds
were controlled by herbicides, and grass sward was mown 5–7 times during vegetation
period in alleyways. Ammonium nitrate was applied 50 g per tree in every spring.
On the experimental trees the number of inflorescences and fruits were counted,
yield (harvested and weighed per tree in kilograms) weighed. Trunk diameter measured
at a height of 30 cm and converted to trunk cross-sectional area (TCSA). The length
of top shoot was measured in 2005. The results were evaluated statistically using the
analysis of variance. The significance of differences between the variants was estimated
at 0.05 level (Duncan’s multiple range test).
Length of the vegetation period is 175–180 days and mean active temperature
sum ranges within 1400–1900 in experimental place. Average amount of precipitation
during the vegetation period is 450–500 mm. The weather conditions in 2002–2004
were unfavourable for the cropping of apple trees. The summer of 2002 was extremely
hot and dry (only 28.9 mm rain fell in the period from July 7 to August 31). The
spring of 2003 was colder than usual and spring frosts (–1.3°C) occurred in the first
decade of June. In 2004 severe frosts occurred (–4.5°C and –3.0°C) during the
flowering time and almost all flowers were killed. Experimental trees have not been
damaged due to winter frosts during the trial period.
Results. The trees developed flower buds in the first growing season and in
next year cultivars started to bloom. Cultivars ‘Meelis’, ‘Sinap Orlovskij’ and
‘Talvenauding’ formed more flowers than ‘Alro’ and ‘Cortland’ (Table 1). It was
noted that flower formation was affected by rootstock. Cultivars that were grafted
on rootstocks E.75 and M.26 bloomed poorly, while trees on B.9 and B.545 formed
more flowers, especially on cultivars ‘Meelis’ and ‘Sinap Orlovskij’. The amount of
flowers increased every year.
193
T a b l e 1. Average amount of inflorescences in 2002
1
l e n t e l ë.
Vidutinis þiedynø kiekis 2002 m.
Rootstock / Poskiepis
Cultivar
Veislë
M.26
E.75
B.9
B.545
B.396
‘Alro’
‘Cortland’
‘Sinap Orlovskij’
‘Meelis’
‘Talvenauding’
0.2 a
0.2 a
3.2 a
5.6 a
1.4 a
0a
0a
2.4 a
2.4 a
2.2 a
2.2 b
5.4 c
10.6 b
13.2 d
10,6 d
0.8 a
0a
12.1 c
12.5 d
5.2 b
0a
1.9 b
3.3 a
8.4 c
6.8 c
Average / Vidurkis
2.1 a
1.4 a
8.4 d
6.1 c
4.1 b
Mean difference in columns by Duncan test, at α=0.05
Vidutinis skirtumas skiltyse pagal Dunkano kriterijø, kai α=0,05.
The growth performance and number of inflorescences are represented in
Table 2. The growth and blooming of trees started to depend more on rootstock of
the same cultivar. For example, trunks of ‘Sinap Orlovskij’ were significantly thicker
on rootstock B.545 in 2005. These trees developed averagely 114 inflorescences per
tree. At the same time TCSA of trees ‘Sinap Orlovskij’ on rootstocks B.9, B.396 and
M.26 were 2–3 times smaller, yet abundance of blossoming of the trees on these
rootstocks was the same. This shows that rootstocks B.9, B.396 and M.26 inhibit
tree growth and increase flower bud formation.
T a b l e 2. Effect of rootstock on tree size (expressed as TCSA) and
number of inflorescences of trees ‘Sinap Orlovskij’
(2002–2005)
2
l e n t e l ë. Poskiepio átaka ‘Sinap Orlovskij’ veislës vaismedþiø dydþiui ir
þiedynø skaièiui 2002–2005 m.
Rootstocks
Poskiepiai
TCSA
Number of inflorescences per tree
2
Þiedynø skaièius ant medþio
Kamieno skerspjûvio plotas, cm
2002
2003
2004
2005
2002
2003
2004
2005
M.26
E.75
1.8 a
1.7 a
3.3 ab
3.9 b
6.3 abc
7.2 bc
10.6 c
12.1 d
3a
2a
24 bc
10 a
35 b
14 a
136 b
118 a
B.9
B.545
B.396
1.4 a
1.1 a
1.3 a
2.5 a
5.5 c
2.8 ab
4.5 a
10.7 d
4.6 ab
6.8 a
19.1 e
7.8 b
11 b
12 b
3a
16 ab
33 c
35 c
32 b
32 b
39 b
128 b
114 b
182 c
Mean difference in columns by Duncan test, at α=0.05
Vidutinis skirtumas skiltyse pagal Dunkano kriterijø, kai α=0,05.
According to average data of 2002, 2003 and 2005, ‘Sinap Orlovskij’ exceeds
other cultivars by its cumulative yield (Figure 1). In the second-fourth years in the
orchard trees on rootstocks E.75 were the least productive. Trees on rootstocks
B.9, B.396 and M.26 were the most productive. The better rootstock cultivar
combinations were trees ‘Sinap Orlovskij’ on B.396 (8.1 kg), M.26 (7.7 kg), B.9
(6.0 kg) and trees ‘Talvenauding’ on M.26 (6.2 kg) and B.9 (6.1 kg).
194
F i g. 1. Avearge yield (kg per tree) (2002–2005)
1
p a v. Vidutinis derlius 2002–2005 m., kg/vaism.
It could be supposed that yield per tree depend somewhat on vegetative growth
of tree, what in turn is influenced by cultivar, rootstock and their compatibility. To
characterize the growth of trees there were measured the length of top shoot and
trunk diameter. According to data of 2005 the average length of top shoot was 45
cm. The stronger growth was found of trees ‘Alro’, which top shoots were 51 cm
long (Table 3). It was statistically determined that tree growth was affected by
rootstock. Rootstocks E.75, B.9 and B.396 decreased shoots growth of the trees.
Top shoots of trees were longer on rootstocks B.545 and M.26 (50 and 51 cm,
respectively). The same tendency with some exceptions occurred in particular scion/
rootstock combinations also. Trunk diameter was almost equal in all variants at the
beginning of trial, but some differences between rootstocks recorded already in
third growing year and trunk diameter of trees ‘Sinap Orlovskij’ was different in all
variants in the 5th year after planting (Table 2). The smallest average trunk diameter
of all cultivars was on B.9 and B.396 and the largest on B.545 (Table 3). Trunk
diameter of trees ‘Meelis’ and ‘Talvenauding’ was smaller than that of trees ‘Alro’
and ‘Sinap Orlovskij’.
Vegetative growth of tree had some influence upon the yield per tree, as showed
the measurements of 2005. The coefficients of correlation (r) among vegetative
growth statisticians (trunk diameter and top shoot length) varied on a large scale
(r = –0.7-0.93). The weighed correlation coefficient for trunk diameter and top
shoot length of investigated rootstocks was r=0.65 and for trunk diameter and yield
per tree was r=0.51. The average values of “r” suggest that yield depends on some
other significant variables. One characteristic that may have some influence on yield
is fertilization of flowers in young orchard. By example of cultivar ‘Sinap Orlovskij’
we can state that fruit set percentage depends on number of flowers per tree
(Fig. 2). As the number of bees depend on the density of flowers per tree, we can
say that bees visited lesser trees that flowered poorly and it resulted in poor fruit set
195
of these trees as well. Trees which formed 400-800 flowers became attractive for
pollinators. The fruit set was moderate and only 2-4% of total amount of flowers
remained on apple trees that flowered poorly irrespective of scion/rootstock
combination.
T a b l e 3. Average length of top shoot (cm) and trunk diameter
(mm) in 2005
3
l e n t e l ë. Vidutinis virðûnës ilgis (cm) ir vidutinis kamieno skersmuo (mm)
2005 m.
Cultivar
Veislë
Top shoot length
Trunk diameter
Virðutinës atþalos ilgis, cm
Kamieno skersmuo, mm
M.26
E.75
B.9
B.545
E.75
B.9
B.545
B.396
‘Alro’
Sinap Orlovskij’
59 b
47 b
43 a
37 a
46 a
43 b
64 c
48 c
44 a
45 b
33 b
37 c
38 c
39 d
28 a
29 a
47 d
49 e
35 b
32 b
‘Meelis’
‘Talvenauding’
49 c
50 c
40 b
40 a
34 a
38 a
42 b
44 b
42 b
40 a
31 c
32 c
32 c
29 b
25 a
26 a
38 d
34 d
28 b
29 b
Average / Vidurkis
51 b
40 a
40 a
50 b
43 a
33 c
34 c
27 a
42 d
31 b
B.396 M.26
Mean difference in columns by Duncan test, at α=0.05
Vidutinis skirtumas skiltyse pagal Dunkano kriterijø, kai α=0,05.
2
F i g. 2. Correlation between fruit set and amount of inflorescences of ‘Sinap
Orlovskij’ in 2005
p a v.
‘Sinap Orlovskij’ veislës vaisiø uþuomazgø ir þiedynø skaièiaus koreliacija
2005 m.
Cultivars differed on average fruit weight (Table 4). Fruits of cultivars ‘Alro’,
‘Meelis’ and ‘Sinap Orlovskij’ were very big-sized (over 175 g). Reliably smaller
fruits produced trees on rootstock E75, and reliably bigger on M.26 when comparing
fruit weights on other rootstocks.
196
T a b l e 4. Average fruit weight (g) in 2005
4
l e n t e l ë. Vidutinë vaisiaus masë 2005 m., g
Rootstock / Poskiepis
Cultivar
Veislë
Average of cultivars
M.26
E.75
B.9
B.545
B.396
Veisliø vidurkis
‘Alro’
‘Sinap Orlovskij’
‘Meelis’
‘Talvenauding’
204 c
191c
202c
119ab
189 b
142a
166a
123b
173 a
187b
187b
123b
211c
191c
166a
110a
166a
181b
190b
123b
189
178
182
120
Average of rootstock
179 c
155a
168b
170b
165b
167
Poskiepio vidurkis
Discussion. Rootstock effect on characteristics of tree vegetative growth
revealed itself already in the third year of growth, but delineated up till the fifth year
of growth. It appeared that tree growth was weaker on rootstocks B.9 and B.396,
below the medium on M.26 and E.75, and with medium vigour on rootstock B.545.
On the basis of tree top shoot length, B.9, B.396 and E.75 were classified as dwarfing
rootstocks. It is also in agreement with the results of some other authors. Cultivars
on rootstock B.396 grew weaker than these on B.118 and growth vigour of cultivars
‘Renet Simirenko’ and ‘Royal Red Delicious’ on rootstock B.545 was average in
Byelorussia trials (Ignatkova, 2004). Tree growth has not been influenced by the
yield of the first cropping years, because the correlation of tree growth and yield
was of medium strength. Apple trees on rootstocks B.9, B.396 and M.26 yielded
better during five years in orchard. The former literature data from Ukraine (Melnyk
et al., 1999), and Poland trials with B.396 and M.26 (Kurilus, Ugolik, 1999) confirm
our results. Fruit weight was affected by rootstock in young orchard where trees
are not overloaded with crop. Fruits grown on M.26 were bigger than other rootstocks
in our trial. Albeit Tomala et al. (1999) observed no differences of fruit weight on
different rootstocks in full cropping apple orchard.
Conclusions. 1. Rootstocks B.9, B.396 and M.26 inhibit vegetative growth of
tree and increase flower bud formation.
2. According to fruit weight, cultivars on rootstock M.26 produce the largest
fruits in young orchard.
3. The best cumulative yield per tree up to 4 years after planting was obtained
from following scion/rootstock combinations: ‘Sinap Orlovskij’ on B.396 and M.26,
‘Talvenauding’ on M.26 and B.9, ‘Meelis’ on B.9 and B.396, ‘Alro’ on B.545 and
M.26.
Gauta
2006 04 19
Parengta spausdinti
2006 07 13
197
References
1. H a a k E., J a l a k a s M. On apple rootstock evaluations in orchard
experiments in Estonia // Journal of Agricultural Science. 2001. 12(1). P. 8-13.
2. H a a k E. The effect of clonal rootstocks and interstem to the growth and yield
of apple trees // Journal of Agricultural Science. 2003. 14(5). P. 251-259.
3. H u l k o I. P., H u l k o B. I. Orchard performance of apple trees on different
clonal rootstocks // Proceedings of the International Seminar “Apple rootstocks for
intensive orchards” Warsaw-Ursynow, Warzawa, 1999. P. 43-44.
4. I g n a t k o v a N. V. Growth and yielding of apple cultivar-rootstock
combinations // Scientific works of the Institute for Fruit Growing of the National Academy
of Siences of Belarus. Fruit-Growing. Vol. 16. Samohvalovichi, 2004. P. 66-72.
5. K u r i l u s R., U g o l i k M. Effect of rootstocks on growth and yielding of
‘Ðampion’ apple trees // Proceedings of the International Seminar “Apple rootstocks for
intensive orchards”. Warsaw-Ursynow, Warzawa, 1999. P. 65-66.
6. M e l n y k O. V., G o n c h a r u k V. J., T s y r t a V. S., O s a d c h i
V. O. A study of apple rootstocks in intensive orchards // Proceedings of the International
Seminar “Apple rootstocks for intensive orchards”. Warsaw-Ursynow, Warzawa, 1999.
P. 75-76.
7. T o m a l a K., A n d z i a k J., K o b u s i ñ s k i K., D z i u b a n Z.
Influence of rootstocks on fruit maturity and quality of ‘Jonagold’ apples // Proceedings
of the International Seminar “Apple rootstocks for intensive orchards”. Warsaw-Ursynow,
Warzawa, 1999. P. 113-114.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
192–198.
PENKIØ POSKIEPIØ ÁTAKA KETURIØ VEISLIØ OBELØ AUGIMUI IR
DERLIUI JAUNAME SODE
N. Univer, T. Univer, K. Tiirmaa
Santrauka
2001 m. pavasará Polli sodininkystës tyrimø centre tirtos keturios obelø veislës:
‘Talvenauding,’ ‘Meelis’, ‘Alro’ ir ‘Sinap Orlovskij’, su M.26, B.9, B.545, B.396 ir E.75
vegetatyviniais poskiepiais. Kasmet buvo vertinamas vaisiø derlius ir vegetatyvinis
augimas. B.9, B.396 ir M.26 poskiepiai ið esmës sumaþino obelø vegetatyviná augimà
(kamieno skersmená ir ûgliø ilgá – per pirmuosius ketverius metus), o vaismedþiai su B.545
poskiepiu augo sparèiausiai. Anksèiausiai (antraisiais metais po pasodinimo) derliø pradëjo
duoti veislës su B.9, B.396 ir B.545 poskiepiais. Didþiausias gautas vaismedþiø su B.9 ir
B.396 poskiepiais suminis derlius, kiek maþesnis – vaismedþiø su M.26 poskiepiu. Maþiausià
derliø davë ir smulkiausius vaisius iðaugino obelys su E.75 poskiepiu. Ketverius metus
derlingiausios po pasodinimo buvo ‘Sinap Orlovskij’ veislës obelys su B.396 ir M.26
poskiepiais.
Reikðminiai þodþiai: obelys, vegetatyviniai poskiepiai, veislës, augimas, derlius,
vaisiø kokybë.
198
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 199–206.
THE YIELD AND GROWTH OF APPLE TREE CULTIVAR
‘AUKSIS’ ON DIFFERENT ROOTSTOCKS IN LATVIA
Edgars RUBAUSKIS, Mara SKRIVELE
Latvian Institute of Fruit growing, Graudu 1, Dobele, LV 3701, Latvia.
E-mail: [email protected]; web site: www.ddsis.lv
The experiment was a part of the joint research project with Iowa State University,
USA. The aim of trial was to evaluate the suitability of some apple tree rootstocks for
growing in Latvia and their compatibility with cultivar ‘Auksis’. In 1998 a trial with twoyear-old branched trees was established at the Dobele Horticultural Plant Breeding
Experimental Station. Eight dwarf rootstocks (B.9, B.396, B.491, M.9 EMLA, M.26 EMLA,
Mark, O.3 and CG.10) and four semi-dwarf rootstocks (MM.106, B.118, G.30 and C.6) were
compared in the experiment. The planting distances were 4 × 2 m for dwarf rootstocks and
5 × 3 m for semi-dwarf rootstocks. The trees on dwarf rootstocks were trained in a slender
spindle system, and as freestanding central leader trees on semi-dwarf rootstocks. The
results from 1998 to 2005 showed that the largest yield was obtained from trees on dwarf
rootstock Mark and semi-dwarf MM.106 and G.30. The highest yield efficiency was on
dwarf rootstock B.396, and on semi-dwarf G.30. The increase of trunk diameter, as one of
growth parameter, was the poorest on dwarf rootstock B.491 and B.396, and the biggest
on semi-dwarf rootstock MM.106. Fruit weight differed dependently on rootstocks in
both groups only in some years.
For commercial growing of apple tree cultivar ‘Auksis’ suitable rootstocks can be
B.396, B.9 and MM.106. Rootstocks Mark and G.30 are promising, but they need future
comprehensive trials.
Key words: apple tree, fruit weight, increase of trunk diameter, Malus, yield efficiency.
Introduction. The aim of this trial was to evaluate the suitability of some apple
tree rootstocks for growing in Latvia and their compatibility with cultivar ‘Auksis’.
This cultivar is planted in 10% of apple tree Latvian orchards.
There are not much previous investigations about influence of rootstocks on
the yielding of this cultivar till now. In previous investigation the cultivar showed
significant selectivity for rootstocks in the first years of growing (Ikase, 2000). For
that reason our trial with cultivar ‘Auksis’ included eight dwarf and four semi-dwarf
rootstocks.
In Latvian commercial orchards the most widely used rootstocks are Budagovski
(“B” series) and some of West European rootstocks. Rootstocks from USA and
Canada are tested for the first time in Latvia. Special interest we had in rootstock
199
G.30 (Robinson, Hoying, 2004; Robinson et al., 2004), because it is reported to be
better adapted to the biotic stresses of Ervinia amylovora and other diseases.
Material and methods. In 1998 a trial with two-year-old branched trees was
established at the Dobele Horticultural Plant Breeding Experimental Station in the
south of Latvia. The experiment was planted in sod-podzolic, sandy loam soil. The
orchard of trial was managed traditionally. In the second part of June the fruits were
thinned fair to improve fruit quality only.
Eight dwarf rootstocks (group I): B.9, B.396, B.491, M.9 EMLA, M.26 EMLA,
‘Mark’, O.3 and CG.10, and four semi-dwarf rootstocks (group II): MM.106, B.118,
G.30 and C.6 were compared in the experiment. The planting distances were
4 × 2 m (1200 trees per ha) for dwarf rootstocks and 5 × 3 m (666 trees per ha) for
semi-dwarf rootstocks. The trial had 10 replications – one tree per replication. The
trees on dwarf rootstocks were trained in a slender spindle system, and as freestanding
central leader trees on semi-dwarf rootstocks. As pollinators were planted cultivars:
‘Saltanat’, ‘Antei’ and ‘Belorusskoe Malinovoe’ to separate the replications.
Cultivar ‘Auksis’ (Bandaravièius, 1997; Ikase, 2000) is originated in Lithuania.
The cultivar is productive, with a trend to biennial bearing. Harvest time – midseason,
drops rather easily. Rather good resistance to all diseases. Tree vigour is medium or
smaller.
The meteorological conditions varied in the period of 1998–2005. In this period
the average air temperature was higher (6.1–7.4°C) than the long period average
(5.8°C). During vegetation period (May–September) precipitation was 279–495 mm
(average of long period 367 mm). In the period of experiment the positive temperature
sum during growth season was higher (2 514–2 850°C) than the long period average
(2 444°C).
The following measurements were made and data obtained: trunk diameter
20 cm above grafting union, yield per tree, then calculated trunk cross-sectional area
and yield efficiency, average fruit weight and index of biennial bearing (Skrivele et
al., 2000). In the first year the flower clusters and fruits were counted and yield
calculated.
The obtained data were analyzed using ANOVA. The significant differences
between groups were calculated by Tukey at 95% level and marked by letters a, b
and c.
Results and discussion. V e g e t a t i v e g r o w t h. Only one parameter
of vegetative growth was analysed – increase of trunk diameter, that is easy
transformable to trunk cross sectional area to compute the yield efficiency as next
step.
Statistically significant influence of rootstock on increase of trunk diameter
was found only in the group of dwarf rootstocks (Table 2). It is understandable,
because in this group included, among others, two rootstocks which vigour has
been estimated variously in different places. The vigour of B.491 is estimated as
very dwarf, but M.26 in most cases is between vigour of M.7 and M.9. In our trial
on rootstock M.26 EMLA the increase of trunk diameter was significantly larger
than on other rootstocks in this group during all investigation. The increase of trunk
diameter of B.491 was the smallest; however, it was not significantly different from
200
most other rootstocks of this group. It was significantly smaller than M.9 EMLA.
In the group of semi-dwarf rootstocks the difference of increase of trunk
diameter between rootstocks was comparatively small and not statistically significant
(Table 2). The more vigorous growth had trees on rootstock MM 106, similar to
M 26 EMLA.
Y i e l d i n g. In the first years, that characterize the initiation of yielding,
abundant yield was obtained using rootstock Mark – 2.1 kg per tree, also B.9, M.9
EMLA and O.3 – 1.6 kg per tree in the group of dwarf rootstocks, but lowest on
CG.10 – 0.5 kg per tree. Evaluating both rootstock groups, the largest first yields
were obtained on rootstock G.30 – 3.7 kg per tree per year. Some scientists also
have marked the early start of bearing of this rootstock (Robinson, Hoying, 2004;
Robinson et al., 2004; Wertheim, 1998).
T a b l e 1. Yield of apple tree cultivar ‘Auksis’ dependently on
rootstocks, kg/tree
1
l e n t e l ë.
Poskiepiø átaka ‘Auksio’ veislës obelø derliui, kg/vaism.
Year / Metai
Rootstocks
Poskiepiai
2001
2002
Average
2004
2005
Vidurkis
19.8
15.0ab
32.6b
17.9ab
ab
b
18.2ab
2003
Group I / I grupë
B.9
abc
11.1
11.1
B.396
9.3
bc
12.5
18.0
21.2
30.2
B.491
9.0bc
10.0
14.8
12.3ab
29.9b
15.2ab
M.9 EMLA
11.8ab
8.9
16.5
12.6ab
36.1ab
17.2ab
M.26 EMLA
9.2bc
6.2
19.0
9.9ab
48.2a
18.5ab
Mark
16.7a
13.4
15.8
23.7a
30.9b
20.1a
O.3
9.5bc
10.4
11.0
16.7ab
27.3b
15.0ab
CG.10
5.4c
7.0
13.2
8.1b
31.4b
13.0b
Average / Vidurkis
10.3
9.9
16.0
14.9
33.3
16.9
p-value / p reikðmë
1.02E-04
0.056
0.146
0.023
2.66E-05
0.013
Group II / II grupë
MM.106
8.9b
9.4
26.8ab
10.4
68.3a
24.8a
B.118
6.8b
8.3
14.3b
13.6
35.1b
15.6b
G.30
19.3a
11.5
36.2a
10.0
57.1ab
26.8a
C.6
10.5b
5.3
18.9b
4.9
39.2b
15.8b
Average / Vidurkis
11.4
8.6
24.1
9.7
49.9
20.7
p-value / p reikðmë
1.73E-06
0.125
0.001
0.339
0.001
2.64E-04
Rootstocks ‘Mark’ and G.30 are characterised by fast rise of yield. From apple
trees on rootstock ‘Mark’ there were obtained 16.7 kg, but on rootstock
G.30 – 19.3 kg per tree already in fourth year (Table 1). In next years the apple trees
201
on rootstock Mark yielded stable with some fairly small fluctuations from year to
year, which is represented by a very small index of biennial bearing – 0.23 (Table 2).
As a result the apple trees on this rootstock had the largest total yield in the group of
dwarf rootstocks (Figure). The total yield of apple trees was bigger on rootstock
G.30, however, those trees yielded more biennially (index of biennial bearing – 0.60)
(Table 2).
T a b l e 2. Growth and yield parameters dependently on rootstocks
2
l e n t e l ë. Augimo ir derliaus rodikliø priklausomumas nuo poskiepiø
Rootstocks
Poskiepiai
Increase of trunk
diameter (1998–2005)
Kamieno skersmens
padidëjimas 1998–2005 m.,
mm
Average
productivity
(2001–2005)
Vidutinis derlius
2001–2005 m., t/ha
Average fruit Index of biennial
bearing (2000–
weight
2005)
Vidutinë
Prameèiavimo
vaisiaus masë,
indeksas
g
2000–2005 m.
Group I / I grupë
B.9
bc
21.5ab
187
0.41ab
bc
ab
49.2
B.396
46.8
21.8
180
0.23b
B.491
44.6c
18.2ab
190
0.43ab
M.9 EMLA
55.3b
20.6ab
193
0.45ab
M.26 EMLA
70.3a
22.2ab
202
0.64a
Mark
50.5bc
24.1a
197
0.23b
O.3
47.5bc
18.0ab
194
0.26ab
bc
b
CG.10
52.9
15.6
210
0.49ab
Average / Vidurkis
52.1
20.3
194
0.39
p-value / p reikðmë
7.51E-14
0.387
0.014
0.013
Group II / II grupë
MM.106
B.118
G.30
C.6
76.7
16.5a
188
0.63
59.6
b
198
0.38
a
203
0.60
b
202
0.69
198
0.56
10.4
65.2
17.8
60.1
Average / Vidurkis
65.4
p-value / p reikðmë
0.064
10.5
13.8
2.64E-0.4
0.135
0.087
Very slow rise of yield the trees had on rootstock CG.10 (Table 1). In the group
of dwarf rootstocks the total yield was smallest on this rootstock (Figure). The trees
were unfruitful, although regularly bearing, on rootstock O.3 (Table 1). The apple
trees had low increase of yields on rootstock M.26 EMLA (Table 1). They had
biennial bearing (Table 2). The largest yield was obtained just in the last year; as a
result the total yield on this rootstock was the same as on rootstocks B.9 and B.396
(Figure). However, in contrary to M.26 EMLA both B.9 and B.396 had positive
202
influence on the regularity of bearing – the indexes of biennial bearing were 0.41 and
0.23, respectively. On these rootstocks the apple trees had slightly larger productivity
than on M.9 EMLA (Table 2).
On rootstock MM.106 the apple trees had a slow rise of yield. Only in the sixth
year of growth they had commercially significant yield – 26.8 kg per tree (Table 1).
They also had irregular yielding, but the total yield was on the same amount as on
rootstock G.30 (Table 2, Figure).
F i g. Total yield per tree and yield efficiency
P a v. Vaismedþio suminis derlius ir produktyvumas
p-value of total yield: for dwarf rootstock group 0.014 and semi-dwarf 1.63E-04 / Suminio derliaus
reikðmë p: þemaûgiø poskiepiø grupë – 0,014, pusiau þemaûgiø – 1,63E-04.
p-value of yield efficiency: for dwarf rootstock group 6.54E-12 and semi-dwarf 0.005 /
Produktyvumo reikðmë p: þemaûgiø poskiepiø grupë – 6,54E-12, pusiau þemaûgiø – 0,005.
Significantly different groups for total yield are marked by grey colour as “a”, grey and white – “ab”
and white – “b” / Suminiu derliumi ið esmës besiskirianèios grupës paþymëtos: pilka spalva – a, pilka
ir balta – ab ir balta – b.
Significantly different groups for yield efficiency are marked by symbols: ¡ as “a”, ® “ab”, Q”b”,
™ “bc” and ˜ “c” / Produktyvumu ið esmës besiskirianèios grupës paþymëtos simboliais:
¡ – a, ®– ab, Q– b, ™– bc ir ˜ – c.
Evaluating the obtained yield per tree of both rootstock groups, the best
productivity was on rootstocks G.30, MM.106, Mark, also on B.396, M.26 EMLA
and B.9 (Figure). On all these rootstocks the trees were more productive than on
M.9 EMLA. Calculating the yield per hectare the first place for productivity got the
rootstocks of group I Mark, B.396, M.26 EMLA and B.9 (Table 2). Similar yield
data of cultivar ‘Auksis’ on rootstock M.26 were obtained in Lithuania (Uselis, 2002),
at slightly larger planting distances – 4 x 2.5 m. Also in previous investigation the
best results were shown by rootstock B.9 (Ikase, 2000).
203
The same situation was observed if rootstocks were evaluated by yield efficiency
(Figure) – respectively total yield per tree (kg) on trunk cross-sectional area (1 cm2).
Then according to the best results came rootstocks B.396, B.491, Mark and B.9. On
the other hand, rootstock M.26 EMLA, which was characterised by large increase
of trunk diameter (Table 2), came with smallest yield efficiency among all rootstocks.
Fruit weight differed statistically significantly dependently on rootstocks in both
groups only in some years. Also the average fruit weight of period 1999-2005 was
the largest, but not statistically significantly different, on rootstocks M.26 EMLA,
CG.10, B.118 and C.6 (Table 2). On the average the smallest fruits produced trees
on rootstock Mark (180 g) and MM.106 (185 g), what could be explained only
partly by the obtained yield on these rootstocks. However, on abundantly bearing
rootstock G.30 the fruits had almost the same size as on unfruitful rootstocks, what
can show direct influence of rootstock on fruit growth.
At the moment rootstocks B.9, B.396, B.118, M.26 and MM.106 are the most
used in Latvia. In this trial the data of yield showed that for the cultivar ‘Auksis’
more suitable could be dwarf rootstocks B.9 and B.396 and semi-dwarf MM.106.
For growing in sandy loam soil rootstocks Mark and G.30 could be suitable for
cultivar ‘Auksis’. These rootstocks must be tested in other growing conditions,
especially in different soil conditions and with other cultivars. As showed investigations
in the USA, rootstock G.30 is resistant to Ervinia amylovora, Phytopthora ssp. and
replant diseases (Robinson, Hoying, 2004; Robinson et al., 2004). In our trials with
rootstock Mark good results were obtained also with cultivar ‘Zarya Alatau’
(Rubauskis, Skrivele, 2004). Rootstock Mark is tolerant to Phytopthora, but not
resistant to Ervinia amylovora; it can be not compatible with triploid cultivars. As
marked by S. J. Wertheim (1998), this rootstock has unequivocal estimation in
different countries.
Conclusions. For commercial growing of apple tree cultivar ‘Auksis’ suitable
rootstocks can be B.396, B.9 and MM.106.
Rootstocks Mark and G.30 are promising, but they need future comprehensive
Mark trials.
The largest yield was obtained from trees on dwarf rootstock and semi-dwarf
rootstocks G.30 and MM.106.
The highest yield efficiency was on dwarf rootstock B.396 and semi-dwarf
rootstock G.30.
Not so good yield parameters were obtained on rootstocks CG.10, C.6 and
O.3.
The influence of rootstocks on fruit average weight was not statistically proved.
Rootstocks Mark, O.3 and B.396 exhibited the lowest bienniality of bearing.
The higher biennial bearing cv. ‘Auksis’ had on rootstocks M.26 EMLA, MM.106
and C.6.
Gauta
2006 05 04
Parengta spausdinti
2006 07 18
204
References
1. B a n d a r a v i è i u s A. Obelø veislës. Babtai: Lietuvos sodininkystës ir
darþininkystës institutas, 1997. P. 96.
2. I k a s e L. Production and fruit quality of 5 apple varieties on 5 clonal rootstocks
in Dobele, Latvia. // Proceedings of the international conference “Fruit production and fruit
breeding”. Fruit Science. 2000. Nr. 207. Tartu: Estonian Agricultural University. P. 20–23.
3. R o b i n s o n T. L., A n d e r s o n L., A z a r e n k o A., D o m o t o
P. et al. Performance of Cornell-Geneva rootstocks across North America in multi-location
NC-140 rootstock trials // Proc. Ist international symposium on rootstocks for deciduous
fruit tree species. Eds. M. A. Moreno Sanchez and A. D. Webster. Acta Horticulturae 658.
2004. Leuven: ISHS. P. 241–245.
4. R o b i n s o n T. L., H o y i n g S. A. Performance of elite Cornell Geneva
apple Rootstocks in long-term orchard trials on growers farm // Proc. Ist international
symposium on rootstocks for deciduous fruit tree species. Eds. M. A. Moreno Sanchez
and A. D. Webster. Acta Horticulturae 658. 2004. Leuven: ISHS. P. 221–230.
5. R u b a u s k i s E., S k r i v e l e M. Evaluation of some dwarf rootstocks
forms in Latvia. // Material of 8th International symposium on integrating canopy, rootstock
and environmental physiology in orchard systems. Hungary, Budapest, June 13–18, 2004
(in print).
6. S k r i v e l e M., D i m z a I., R u b a u s k i s E. The cropping of nine
apple cultivars as influenced by two different rootstocks. // Proceedings of the international
conference “Fruit production and fruit breeding”. Fruit Science. 2000. Nr. 207. Tartu: Estonian
Agricultural University. P. 100–103.
7. U s e l i s N. Assessment of productivity and fruit quality of apple cultivars on
rootstock M 26 in fruit bearing orchard. // Scientific works of the Lithuanian Institute of
Horticulture and Lithuanian University of Agriculture. Horticulture and vegetable growing.
2002. 21(3). Babtai: Lithuanian Institute of Horticulture. P. 14–28.
8. W e r t h e i m S. J. Rootstock guide apple, pear, cherry, European plum.
Wilhelminadorp: Fruit Research Station. 1998. P. 144.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
199–206.
‘AUKSIO’ VEISLËS OBELØ SU SKIRTINGAIS POSKIEPIAIS AUGIMAS IR
DERËJIMAS LATVIJOJE
E. Rubauskis, M. Skrivele
Santrauka
Bandymas buvo bendro tyrimø projekto su Javos valstybiniu universitetu (JAV)
dalis. Jo tikslas – ávertinti kai kuriø obelø poskiepiø tinkamumà auginti Latvijoje ir jø
suderinamumà su ‘Auksio’ veisle. Tyrimas pradëtas 1998 metais Dobeles sodininkystës
tyrimø stotyje. Lyginti aðtuoni þemaûgiai (B.9, B.396, B.491, M.9 EMLA, M.26 EMLA,
Mark, O.3 ir CG.10) ir keturi pusiau þemaûgiai (MM.106, B.118, G.30 ir C.6) poskiepiai.
Þemaûgiai poskiepiai buvo pasodinti 4 × 2 m, pusiau þemaûgiai – 5 × 3 m atstumais.
Vaismedþiø su þemaûgiais poskiepiais vainikai buvo suformuoti laibos verpstës formos,
205
su pusiau þemaûgiais – aðiniai. 1998–2005 metø rezultatai parodë, jog didþiausià derliø
davë obelys su þemaûgiu poskiepiu Mark ir pusiau þemaûgiais poskiepiais MM.106 ir
G.30. Produktyviausi buvo vaismedþiai su þemaûgiu poskiepiu B.396 ir pusiau þemaûgiu
G.30. Maþiausias buvo vaismedþiø su þemaûgiais poskiepiais B.491 ir B.396 kamieno
skersmens padidëjimas, kaip vienas ið augimo rodikliø, didþiausias – su pusiau þemaûgiu
poskiepiu MM.106. Abiejose poskiepiø augumo grupëse poskiepiai turëjo átakos vaisiø
masei tik kai kuriais metais.
‘Auksio’ veislës obelims auginti versliniuose soduose gali bûti tinkami ðie poskiepiai:
B.396, B.9 ir MM.106. Mark ir G.30 poskiepiai yra perspektyvûs, taèiau jie turi bûti iðsamiai
iðtirti.
Reikðminiai þodþiai: obelys, vaisiø masë, kamieno skersmens didëjimas, Malus,
produktyvumas.
206
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 207–211.
THE INFLUENCE OF ROOTSTOCK ON PRODUCTIVITY
AND FRUIT QUALITY OF APPLE-TREE CULTIVAR
‘FLORINA’ UNDER CONDITIONS OF SOUTH RUSSIA
Vasiliy OSTAPENKO
Kuban State Agricultural University, Kalinin str. 13, 350044, Krasnodar,
Russia. E-mail: inform@kubagro
Under conditions of field experiment laid on leached chernozems of the Prikubansky
(South Russia) horticultural zone the influence of rootstocks on the most important
components of apple tree fruit quality was studied. There was studied cultivar ‘Florina’ on
rootstocks M.9, M.26, MM.106. The orchard was planted according to the scheme 4 x 2 m.
Experiment showed that the character of change of apple tree fruit quality is determined
by growth vigour of the used rootstocks. When inoculated on dwarf rootstocks M.26 and
M.9 the yield of cultivar ‘Florina’ per tree increased by 30% and 60%, correspondingly.
Besides, the yield of the cultivar on these rootstocks was 10% greater than on the rootstocks
MM.106. When using semi-dwarf rootstock MM.106 the content of vitamins C and P as
well as pectins increased greatly.
Key words: apple-tree, rootstocks, productivity, market quality, biochemical indices.
Introduction. One of the major tasks of the Russian Federation horticulture is
to work according to arrangement and to supply high and hardy fruit yields, what
has already become traditional (Êóäðÿâåö,1987).
In such situation many producers prefer to create highly productive plantations
of intensive type, providing the essential increase of gross production and low cost
price of fruits, as well as quick justifying of costs (Ãóäêîâñêèé,1999).
According to specialists, produced products mostly are less competitive. From
the whole amount of obtained apples and other fruits only about 30% of fruits meet
the requirements of high and the first trade varieties today (Êàøèí, 2003; Øèäàêîâ,
2003).
It is obvious, that increase of plantation productivity and fruit production quality
are two relatively independent tasks, frequently counteracting each other. For example,
well-known fact of significant decrease of fruit mass under too high tree load with
fruit witnesses the given statement.
The problem of fruit quality increase has a great significance under conditions
of occurred structural changes in state economics and intensivity of competitiveness
207
among producers (Êóõàåâ, 1997). It is connected with the growing demands of
consumers, determining the market cost of fruit production, and finally – the size of
possible economic effect. The objective of researches was to study rootstock
influence on productivity and apple-tree fruit quality under the conditions of South
Russia.
Material and methods. Researches were carried out in 2000–2005 under the
conditions of field experiment, laid on leached chernozems of Prikubanskiy horticultural
zone (South Russia). The object of study was apple tree cultivar ‘Florina’, inoculated
on vegetative propagated dwarf rootstocks M.9 and M.26 and the semi-dwarf
MM.106.
The orchard was planted in 1998; the scheme of planting is 4 x 2 m.
Calculations and observations were carried out by generally accepted methods
(Ïðîãðàììà è ìåòîäèêà, 1999).
Results. The conducted investigations showed that rootstock essentially
influenced the productivity of cultivar and fruit quality (Table 1). So fruit yield of
‘Florina’ on rootstock M.9 was 23% higher that on M.26 and 39% bigger than using
semi-dwarf rootstock MM.106. The mass of fruit using the rootstocks M.9 and
M.26 was by 8-10% higher than the mentioned indexes on semi-dwarf rootstock
MM.106. Moreover, there was obtained by 10% more the supreme and the first
market varieties than using dwarf trees.
T a b l e 1. Influence of rootstock on productivity and fruit quality of
apple tree cultivar ‘Florina’, average of 2000–2005
1
l e n t e l ë. Poskiepio átaka ‘Florina’ veislës obelø derlingumui ir vaisiø
kokybei, 2000–2005 m. vidurkiai
Rootstock
Yield,
kg/tree
Average fruit
mass
Fruit quality classes / Vaisiø kokybës klasë, %
extra
first
second
below
second
Derlius,
kg/medis
Vidutinë vaisiaus
masë, g
aukšèiausioji
rûðis
pirmoji rûðis
antroji rûðis
Ì.9
Ì.26
ÌÌ.106
18.9
14.7
11.7
145
142
140
62
61
56
15
16
20
18
17
21
5
6
3
LSD05 / R05
2.4
0,9
-
-
-
-
Poskiepis
kitos
Research showed that rootstock influences the content of dry soluble solids
and biologically active substances in fruit (Table 2).
The biggest content of dry matter and sucrose was noticed in fruits of cultivar
‘Florina’ on rootstock M.9. The use of semi-dwarf rootstock MM.106 allowed
essentially to increase the content of vitamins C and P in fruits of this cultivar, as
well as the building up of pectins.
208
T a b l e 2. Biochemical indices of fruit quality of apple tree cultivar
‘Florina’ depending on rootstock, 2003–2005
2
l e n t e l ë.
Rootstock
‘Florina’ veislës obelø vaisiø kokybës biocheminiø rodikliø
priklausomumas nuo poskiepio, 2003–2005 m.
Dry soluble solids
Total amount of
sucrose
Sausosios tirpiosios
medžiagos, %
Bendras sacharozës
kiekis, %
Ì.9
Ì.26
ÌÌ.106
13.1
12.9
12.4
4.21
3.85
3.89
LSD05 / R05
0.1
-
Poskiepis
Acidity
Rûgðtumas,
%
Vitamins
Vitaminai,
mg/100 g
Total amount
of pectins
Bendras pektinø
kiekis, %
Ñ
Ð
0.4
0.5
0.5
3.71
3.45
3.89
29.7
27.7
30.6
0.47
0.47
0.53
-
0.2
0.7
-
Discussion. Discussing the problem of fruit quality, it is necessary to pay
attention to the following fact. There is no doubt that every branch of agriculture is
urged to implement its own specific functions in modern society. It must provide
population with foodstuffs, having curative properties and helping to prevent many
diseases (Ôðàí÷óê, 1968). However, most fruit producers don’t have information
about the chemical content of foodstuffs, as well as about content of biologically
active substances (Ñàâåëüåâ, Ëåîí÷åíêî, 2005).
One should mention for the comparison, that when growing wheat, we aim to
increase the protein content in grain, and we purposefully increase the sunflower
seed oil, and concentration of sucrose in sugar beet.
At the same time the qualitative traits of fruit (except sizes) remain without
attention in the process of fruit-tree planting. This essentially decreases their nutritional
qualities.
The above-mentioned fact makes us to think seriously of the given situation and
to do the corresponding amendments in the strategy of branch development. The
complex of agrotechnical method, providing the possibility to regulate purposefully
the separate indices of fruit quality during their formation must be offered within the
adaptive and organic horticulture.
One of these techniques, influencing not only growth vigor of tree, but also the
amount of yield, as well as market fruit quality, is right selection of optimal rootstock
(Áàêóåâ, 2004).
As the experiment showed, the character of indices of apple-tree productivity
and quality is determined by growth vigor of rootstocks. The productivity of cultivar
‘Florina’ increased using dwarf rootstocks, as well as obtaining supreme and qualitative
fruits. Under such condition, rootstock M.9 can accumulate much dry matter and
sucrose in fruits, what influences the taste qualities. However, content of biological
active substances (BAS) in fruits of this rootstock is lower than using semi-dwarf
rootstock MM.106. Consequently, in order to get fruits rich with vitamins and pectins,
we should apply for cultivar ‘Florina’ semi-dwarf rootstock MM.106.
Conclusion. It is necessary to select rootstocks for purposeful production of
apples with given parameters of fruit quality.
Usage of dwarf rootstocks M.9 and M.26 allows to increase fruit yield of cultivar
209
‘Florina’ by 30–60% and to get by 10% more fruits of Extra quality apples in
comparison with these indices of trees on semi-dwarf rootstock MM.106.
M.9 and M.26 increase accumulation of dry matter in fruits.
The application of semi-dwarf rootstock MM.106 helps to increase in fruits the
content of vitamins C and P as well as pectins.
Gauta
2006 03 24
Parengta spausdinti
2006 07 25
References
1. Á à ê ó å â Æ. Õ. Ïðèåìû ïîâûøåíèÿ óðîæàéíîñòè ÿáëîíè íà
êëîíîâûõ ïîäâîÿõ â ïðåäãîðüÿõ ÊÁÐ/ Ïðîáëåìû ýêîëîãèçàöèè ñîâðåìåííîãî
ñàäîâîäñòâà è ïóòè èõ ðåøåíèÿ: ìàòåðèàëû ìåæäóíàð.êîíô. Êðàñíîäàð.
2004. Ñ. 424–431.
2. à ó ä ê î â ñ ê è é Â. À. Íàó÷íûå îñíîâû óñòîé÷èâîãî ñàäîâîäñòâà
Ðîññèè / Ñëàáîðîñëîå ñàäîâîäñòâî: Ìåæäóíàð. íàó÷.-ïðàêò. êîíô. 1999.
×. I. Ìè÷óðèíñê. Ñ. 12–15.
3. Ê à ø è í Â. È. Ïðîáëåìà íàó÷íîãî îáåñïå÷åíèÿ ñàäîâîäñòâà
Ðîññèè / Ïëîäîâîäñòâî è ÿãîäîâîäñòâî Ðîññèè: Ñá.íàó÷.-ïðàêò. Ðàáîò /
ÂÑÒÈÑÏ. Ì. 2003. Ñ. 3–37.
4. Ê å õ à å â Â. Ê. Ïðîãíîçèðîâàíèå êîíêóðåíòîñïîñîáíîñòè ïëîäîâ
è ÿãîä/ Ïðîãíîçèðîâàíèå êîíêóðåíòîñïîñîáíîñòè îñíîâíûõ âèäîâ
ïðîäîâîëüñòâèÿ â óñëîâèÿõ Êðàñíîäàðñêîãî êðàÿ: Ñá.ìàòåðèàëîâ íàó÷.ïðàêè÷.êîíôåðåíöèè. Êðàñíîäàð. 1997. Ñ. 58–67.
5. Ê ó ä ð ÿ â å ö Ð. Ï. Ïðîäóêòèâíîñòü ÿáëîíè. Ì. 1987. Àãðîïðîìèçäàòþ.
303 ñ.
6. Ï ð î ã ð à ì ì à è ìåòîäèêà ñîðòîèçó÷åíèÿ ïëîäîâûõ, ÿãîäíûõ è
îðåõîïëîäíûõ êóëüòóð / Ïîä ðåä. Å. Í. Ñåäîâà è Ò. Ï. Îãîëüöîâîé.
Îðåë. 1999. 502 ñ.
7. Ñ à â å ë ü å â Í. È., Ë å î í ÷ å í ê î Â. Ã. è äð. Áèîõèìè÷åñêèé
ñîñòàâ ïëîäîâ è ÿãîä è èõ ïðèãîäíîñòü äëÿ ïåðåðàáîòêè. Ìè÷óðèíñê.
2004. 124 ñ.
8. Ñ å ä î â Å. Í. Ñåëåêöèÿ è ñîðòèìåíò ÿáëîíè äëÿ Öåíòðàëüíûõ
ðåãèîíîâ Ðîññèè. Îðåë: Èçä-âî ÂÍÈÈÑÏÊ. 2005. 312 ñ.
9. Ø è ä à ê î â Ð. Ñ. Îïòèìèçàöèÿ ñîðòèìåíòà ÿáëîíè òåõíè÷åñêîãî
íàçíà÷åíèÿ â àãðîëàíäøàôòàõ Ñåâåðíîãî Êàâêàçà / Îïòèìèçàöèÿ ïîðîäíîñîðòîâîãî ñîñòàâà è ñèñòåì âîçäåëûâàíèÿ ïëîäîâûõ êóëüòóð: Ñá.íàó÷.
òðóäîâ. Êðàñíîäàð: ÑÊÇÍÈÈÑèÂ. 2003. Ñ. 104–114.
10. Ô ð à í ÷ ó ê Å. Ï. Òîâàðíûå êà÷åñòâà ïëîäîâ. Ì. 1968. 269 ñ.
210
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
207–211.
POSKIEPIO ÁTAKA ‘FLORINA’ VEISLËS OBELØ DERLINGUMUI IR
VAISIØ KOKYBEI PIETØ RUSIJOS SÀLYGOMIS
V. Ostapenko
Santrauka
Lauko bandymas árengtas Prikubanës (Pietø Rusija) sodininkystës zonoje. Tirta
M.9, M.26, MM.106 poskiepiø átaka svarbiausiems ‘Florina’ veislës obuoliø kokybës
rodikliams. Sodas pasodintas pagal schemà 4 x 2 m.
Vaisiø kokybë priklausë nuo poskiepiø augumo. Áskiepijus ‘Florina’ veislës obelis á
þemaûgius poskiepius M.26 ir M.9, kiekvieno vaismedþio derlius padidëjo atitinkamai 30 ir
60%. Be to, vaismedþiø su ðiais poskiepiais derlius buvo 10% didesnis negu su MM.106.
Áskiepijus á pusiau þemaûgá poskiepá MM.106, vaisiuose labai pagausëjo C ir P vitaminø
bei pektinø.
Kad vaisiai atitiktø tam tikrus kokybës rodiklius, svarbu tinkamai parinkti poskiepá.
Reikðminiai þodþiai: obelys, poskiepiai, derlingumas, rinkos kokybë, biocheminiai
rodikliai.
211
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 212–217.
INFLUENCE OF ROOTSTOCK ON GROWTH AND
REPRODUCTIVE CHARACTERISTICS OF CHERRY
CULTIVAR ‘STELLA’ DURING THE PERIOD OF
COMPLETE FRUITING
Alexandros PAPACHATZIS
Agricultural University,12 Mendeleev str., 4000 Plovdiv, Bulgaria.
E-mail: [email protected]
During the period of 2004–2005 the rootstocks Gisela 5, Gisela 4, Weiroot 10, Weiroot
13, Weiroot 53, Weiroot 72, Weiroot 158 and P 1 (the Bulgarian selection of P. mahaleb L.)
as well as selections of Giessen series – Gi-195/20 and Gi-497/8 were tested for cherry
cultivar ‘Stella’. The trees planted in the autumn of 1996 in the experimental field of the
Agricultural University in the town Plovdiv, Bulgaria, at distances of 6.0 x 4.5 m, were
trained as free-growing crowns and were abundantly irrigated.
On the basis of the results in the period of full bearing (8th and 9th vegetation after
planting), rootstocks can be determined as: vigorously growing – P 1, Weiroot 10 and
Weiroot 13; semi-dwarfing to dwarfing – Gi-497/8, Weiroot 158, Weiroot 53, Gisela 4,
Gi-195/20 and Weiroot 72; extremely dwarfing – Gisela 5. The greatest number of suckers
was formed on Weiroot 10, Weiroot 13 and Gisela 4; comparatively insignificant number –
on Weiroot 53, Weiroot 72 and Weiroot 158; and no suckers at all on the remaining ones
– P1, Gisela 5, Gi-195/20 and Gi-497/8. Weiroot 53 and Weiroot 72 induced the highest
productivity in the trees, whereas P 1 induced the lowest.
Key words: sweet cherry, rootstocks, Gisela, Weiroot, growth, fruiting.
Introduction. During the last 10–20 years the world selection created a
comparatively great number of new rootstocks for cherries (Bujdoso, Hrotko, 2005;
Wertheim, 1998), which are nowadays the object of examination under different
soil-climatic conditions in many countries (Bujdoso et al., 2004; Lichev, Lankes,
2003; Reisen, Lander, 1998). For the time being the rootstocks of the series Gisela
(Franken – Bembenek et al., 1999; Gutzwiler, Lang, 2001) and Weiroot (Gutzwiler,
Lang 2001) created in Germany provoke the greatest interest. Certain rootstocks of
these series were introduced in Bulgaria in 1995; they were grafted and the trees
obtained in the course of 9 years were observed in connection with their growth and
reproductive characteristics. The results concerning the influence of rootstocks on
the performance of cherry trees during the periods of vigorous growth and initial
and rapidly increasing fruit-bearing, were published earlier (Lichev, Lankes, 2003,
212
2004). In the present article we report data on the development of the experimental
trees of cultivar ‘Stella’ during the period of full bearing.
Materials and methods. The investigations were conducted during the period
of 2004–2005 with the trees of cherry cultivar ‘Stella’ grafted on in vitro propagated
rootstocks Gisela 5, Gisela 4, Weiroot 10, Weiroot 13, Weiroot 53, Weiroot 72 and
Weiroot 158 and the selections Gi-195/20 and Gi-497/8 of the Giessen series. The
trees of the same cultivar grafted on the seedlings of rootstock P1 (standard Bulgarian
selection of P. Mahaleb L.) were used as control. The experimental plants (6 in
number per variant, using a randomized block design), were planted in the autumn
of 1996 in the experimental field of the Department of Fruit growing at the Agricultural
University in the town Plovdiv at planting distances of 6.0x4.5 m. The trees were
trained as free-growing crowns, grown under the conditions of herbicide treated
fallow land and were irrigated. Plants were cut back after planting at a height of
90 cm, after which they were left to manifest freely their growth and reproductive
characteristics. After completing the training of the crowns, the trees were submitted
to winter pruning every year except the season of 2004-2005.
The region of the experimental plantation is characterized by comparatively
mild winter and dry hot summer, with maximum temperatures in July and August
often reaching 40°C. The yearly precipitation sum total (400–500 mm) was distributed
irregularly, mainly in winter, spring and autumn. The soil was slightly alkali with
pH=7,5 and with medium sandy – loam mechanical composition.
Results. At the end of 9th vegetation after planting, the trees on rootstocks P1,
Weiroot 10 and Weiroot 13 had the thickest trunks whereas those on rootstock
Gisela 5 had the thinnest ones, the remaining variants having intermediate values
(Table 1).
T a b l e 1. Growth characteristics of sweet cherry cultivar ‘Stella’
grafted on different rootstocks, at the end of 9th vegetation
period (2005)
1
l e n t e l ë. ‘Stela’ veislës vyðniø su skirtingais poskiepiais augimo savybës
devintojo vegetacijos laikotarpio pabaigoje 2005 m.
Rootstocks
Trunk cross section area
Poskiepiai
Kamieno skerspjûvio plotas, cm
Tree height
Vaismedžio aukštis, cm
Crown width
Vainiko plotis, cm
P1
Gisela 5
Gisela 4
Gi-195/20
Gi-497/8
Weiroot 10
Weiroot 13
Weiroot 53
Weiroot 72
Weiroot 158
240.3
50.8
117.8
117.3
145.8
236.8
220.6
133.2
112.0
151.2
459.7
231.2
328.5
346.3
393.3
448.8
496.7
345.8
387.5
361.8
396.7
163.1
280.2
285.1
308.3
377.8
386.7
324.1
309.4
320.0
LSD05 / R05
35.9
41.6
37.6
2
213
The data on the tree sizes (Table 1) generally confirm the above-mentioned
tendency in trunk thickness for distributing the rootstocks in 3 groups depending on
the growth vigour induced by them on the graft. Results also indicate that the plants
on Weiroot 13, P1 and Weiroot 10 are about 4.5–5 m high, which necessitates the
application of ladders for picking of fruit and pruning whereas in the other trees
these manual practices can be carried out without their application needed.
The studied rootstocks showed different tendencies toward suckering (Figure).
Its strongest manifestation was in the rootstocks Gisela 4, Weiroot 10 and Weiroot
13, forming in the inter-row space (1,6 m wide) on the average from 14 to 17 shoots
per tree during one vegetation. The rootstocks Weiroot 53, Weiroot 72 and Weiroot
158 showed a considerably smaller tendency to form suckers (4–6 per tree), whereas
the rest of the plants (on P1, Gisela 5, Gi-195/20 and Gi-497/8) formed no suckers.
F i g. Number of suckers of sweet cherry cultivar ‘Stella’ grafted on different
rootstocks, mean of 2004-2005
P a v. ‘Stela’ veislës vyðniø su skirtingais poskiepiais atþalø skaièius, 2004–2005 m.
vidurkiai
*Note: The number of suckers per tree was estimated only in the inter-row strip of 1.6 m width.
Pastaba: atþalø kiekis matuotas 1,6 m ploèio pomedþio juostoje.
The data in Table 2 indicate that in 2005 the fruit-bearing in all variants was
smaller than that of the previous vegetation, which was due to the partial frostdamage of the flower organs of the experimental trees in the winter and spring of
2004–2005. What makes an impression, however, is that the yield was reduced to
the greatest degree in the trees on Gisela 5.
The biggest yield per tree during two years of study produced the bigger plants
– these on Weiroot 10, Weiroot 13 and P1 (Table 2). Taking into consideration the
fact that there were great differences in the vegetative development between the
studied variants, we consider that the index resulting from the proportion between
the yield per tree and the trunk thickness (Table 2), gives more correct notion about
the fertility of cultivar ‘Stella’. In this respect, the highest productivity of trees was
induced by Weiroot 53 and Weiroot 72, the lowest – by P1 and the remaining rootstocks
(Gisela 5, Gisela 4, Gi-195/20 and Gi-497/8, Weiroot 10, Weiroot 13 and Weiroot
158) had an intermediate position.
214
T a b l e 2. Fruiting of sweet cherry cultivar ‘Stella’ grafted on
different rootstocks, 2004–2005
2
l e n t e l ë. ‘Stela’ veislës vyðniø su skirtingais poskiepiais derlingumas
2004–2005 m.
Yield, kg/tree / Derlius, kg/medis
Rootstocks
Total for 2004–2005
Yield efficiency in 2004–2005
Produktyvumas
Poskiepiai
2004
2005
Suminis 2004–2005 m.
derlius
2004–2005 m., kg/cm2
Ð1
Gisela 5
Gisela 4
Gi-195/20
Gi-497/8
Weiroot 10
Weiroot 13
Weiroot 53
Weiroot 72
Weiroot 158
32.9
12.5
22.5
20.9
22.0
35.9
32.1
29.9
21.9
26.2
28.7
5.8
17.0
16.2
19.7
34.4
31.8
22.9
19.2
21.6
61.6
18.3
39.5
37.1
41.7
70.3
63.9
52.8
41.1
47.8
0.26
0.36
0.34
0.31
0.28
0.30
0.29
0.40
0.37
0.32
LSD05 / R05
9.0
7.2
16.2
0.11
Discussion. To a certain extent, similar differentiation between the studied
rootstocks of Gisela and Weiroot series with respect to their growth vigour, was
conducted by other authors as well after extensive field experiments (Stehr, 1996;
Balmer, 1998; Bujdoso et al., 2004). The results obtained by us differ from those of
indicated foreign authors by the conclusion that in the course of our experiment
Gisela 5 was manifested as too dwarfing and in this respect it was proved to defer to
the other dwarfing rootstocks – Weiroot 53, Weiroot 72 and Weiroot 158. Most
authors comparing the rootstock Gisela 5 with those of the second generation of
Weiroot series (Weiroot 53, Weiroot 72 and Weiroot 158) in the experimental field,
did not establish such a great difference between them with respect to their vegetative
development (Stehr, 1996; Balmer, 1998; Bujdoso et al., 2004).
In connection with sucker-formation potentiality of the examined rootstocks of
Gisela and Weiroot series, other authors also reported similar results in most of them
(Balmer, 1998; Löcher, 1991; Weber, 1992). Other opinions also exist, however,
about some of rootstocks, according to which the trees on Gisela 5 are capable of
forming suckers, if only insignificant in number (Balmer, 1998; Weber, 1992) and
those on Weiroot 158 have no tendency to sucker-formation (Löcher, 1991).
If we make a comparison between the productivity of trees during their 8th and
th
9 vegetation (in 2004 and 2005) and that of the same plants by the end of 6th year
after planting (Lichev, Lankes, 2004), we’ll establish that during the period of full
bearing the priority of Gisela 5 and Gisela 4 decreased, whereas the productive
potentialities of Weiroot 53 increased. In the remaining rootstocks no significant
deviations with respect to their productivity in the two maturity periods were reported.
The results obtained by us about the fertility of the trees on Gisela 5 do not
215
coincide with the opinion of most research workers in the same field, according to
whom this rootstock induces high productivity to the cultivars grafted on it not only
in the period of initial and rapidly increasing fruit-bearing, but at a later time too
(Stehr, 1996).
Conclusions. The results obtained during the period of full bearing (8th and 9th
vegetation after planting) of cultivar ‘Stella’ leads to the following conclusions:
1. Depending on the growth vigour induced to the scion, the rootstocks can be
distributed to three groups: vigorously growing – P1, Weiroot 10 and Weiroot 13;
semi-dwarfing to dwarfing – Gi-497/8, Weiroot 158, Weiroot 53, Gisela 4,
Gi-195/20 and Weiroot 72; extremely dwarfing – Gisela 5.
2. Weiroot 10, Weiroot 13 and Gisela 4 are distinguished by the highest potentiality
for sucker – formation, Weiroot 53, Weiroot 72 and Weiroot 158 – by a low potentiality,
whereas the remaining rootstocks (P 1, Gisela 5, Gi-195/20 and Gi-497/8) – do not
form suckers.
3. The highest productivity was induced to the trees by Weiroot 53 and Weiroot
72 and the lowest – by P 1.
Gauta
2006 05 04
Parengta spausdinti
2006 08 07
References
1. B a l m e r M. Sûsskirschenunterlagen in Bewegung. Deutsche Baumschule.
1998. 10. 37–39.
2. B u j d o s o G., K. H r o t k o, R. S t e h r. Evaluation of sweet and sour
cherry cultivars on german dwarfing rootstocks in Hungary. Journal of Fruit and Ornamental
Plant Research. 2004. Vol. 12. P. 233–244.
3. B u j d o s o G., K. H r o t k o. Effects of rootstock – scion interactions on
dwarf cherry rootstocks in Hungary. Hort. Sci (Prague). 2005. 32, 4. P.129–137.
4. F r a n k e n - B e m b e n e k S., W. G r u p p e, G. L i n k e, H.
S c h m i d t. Rûckblick auf das Zûchtungsprogramm der Gisela – Kirschenunterlagen.
Erwerbsobstbau. 1999. 41. 123–128.
5. G u t z w i l e r J., G. A. L a n g. Sweet cherry crop load and vigor
management on Gisela rootstocks. Acta Horticulturae. 2001. P. 557, 321–325.
6. L i c h e v V., C. L a n k e s. Erste Ergebnisse von Leistungsprûfungen mit
Gisela – und Weiroot – Unterlagen in Bulgarien. Erwerbsobstbau. 2003. 45, 5, 157–161.
7. L i c h e v V., C. L a n k e s. Ergebnisse der Leistugsprûfungen der
Sûsskirschensorte ’Stella‘ auf Gisela – und Weiroot – Unterlagen in Bulgarien. Erwerbs –
Obstbau. 2004. 46, 65–73.
8. L õ c h e r E. Folienabdeckung bei Sûsskirschen. Obst und Garten. 1991. 6.
293–295.
9. R i e s e n W., J. L a d n e r. Hohe Ertrage mit den neuen Kirschenunterlagen.
Obst und Weinbau. 1998. 134, 24. 609–611.
10. S t e h r R. Erste Zwischenergebnisse eines Unterlagenversuchs zu
Sûsskirschen. Erwerbsobstbau. 1996. 38. 122–125.
11. W e b e r A. Wissen Motivieren Kõnnen. Obst und Garten. 1992. 6. 294–298.
12. W e r t h e i m S. J. Rootstock Guide – Apple, Pear, Cherry, European Plum.
Publication no. 25, Fruit Research Station Wilhelminadorp, The Netherlands, 1998.
216
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
212–217.
POSKIEPIO ÁTAKA ‘STELLA’ VEISLËS VYÐNIØ AUGIMUI IR
REPRODUKCINËMS SAVYBËMS DERËJIMO LAIKOTARPIU
A. Papachatzis
Santrauka
2004–2005 metais buvo tirtos ‘Stella’ veislës vyðnios su ðiais poskiepiais: Gisela 5,
Gisela 4, Weiroot 10, Weiroot 13, Weiroot 53, Weiroot 72, Weiroot 158 ir P 1 (Bulgarijos
P. Mahaleb L. selekcija) ir Gi-195/20 bei Gi-497/8 (Giessen serijø selekcija). Sodas áveistas
1996 metø rudená Plovdiv (Bulgarija) þemës ûkio universiteto bandymø lauke, vaismedþius
sodinant 6,0 x 4,5 m atstumais. Formuoti laisvai augantys vaismedþiø vainikai.
Kaip rodo derëjimo laikotarpiu (8–9 vegetacija po pasodinimo) gauti rezultatai,
poskiepiai gali bûti skirstomi á: stipriai auganèius – P 1, Weiroot 10 ir Weiroot 13; pusiau
þemaûgius ir þemaûgius – Gi-497/8, Weiroot 158, Weiroot 53, Gisela 4, Gi-195/20 ir Weiroot
72; nykðtukinius – Gisela 5. Daugiausia atþalø iðaugo ant Weiroot 10, Weiroot 13 ir
Gisela 4, palyginti nedaug – ant Weiroot 53, Weiroot 72 ir Weiroot 158 poskiepiø ir visiðkai
atþalø neturëjo likusieji – P1, Gisela 5, Gi-195/20 ir Gi-497/8 poskiepiai. Derlingiausi buvo
vaismedþiai su Weiroot 53 ir Weiroot 72 poskiepiais, maþiausiai derlingi – su P 1 poskiepiu.
Reikðminiai þodþiai: vyðnios, poskiepiai, Gisela, Weiroot, augimas, derlius.
217
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 218–223.
USE OF GISELA 5 FOR SWEET CHERRIES
Jef VERCAMMEN*, Guy VAN DAELE and Toon VANRYKEL
Pcfruit - Proeftuin pit- en steenfruit, Fruittuinweg 1, 3800 Sint-Truiden,
Belgium. E-mail: [email protected]
By analogy with M.9 for apple, the objective with sweet cherries is to find a dwarfing
rootstock that makes it possible to obtain trees with yield precociously and which are of
reduced stature, so facilitating the harvest of all of the cherries when standing on the
ground. Gisela 5 is a hybrid between Prunus cerasus and Prunus canescens. It is a rootstock
with moderate to weak vigour. The yield efficiency of Gisela 5 is very high, with very good
fruit sizes overall. In dry circumstances cherries can sometimes remain too small. However,
this can be solved quite easily by irrigation of the trees. Gisela 5 is suitable for most
modern varieties. This rootstock is best suited for intensive cherry culture. The original
aim, a smaller easier to control tree, has been achieved with Gisela 5. The trees come into
production earlier, which should shorten the time needed to reach break even on the
orchard investment. It is also easier to intensify and to cover the trees against rain and
birds with Gisela 5.
Key words: dwarfing rootstock, Gisela 5, soil sickness.
Introduction. In modern cherry culture there is no longer a place for very tall
trees. As was the case for apple and pear, the demand for smaller trees, that are
easier to control increased at the end of the seventies and the beginning of the eighties.
In order to achieve this objective a search for dwarfing rootstocks began many
years ago at different research and development locations. By analogy with M.9 for
apple, a rootstock was sought that would make it possible to obtain a tree which
cropped precociously and which was of shorter stature on which the cherries could
be picked when standing on the ground. In Belgium this research led to the introduction
of the GM-rootstocks (Grand-Manil) and in Germany the first Gisela- (Giessen) and
Weiroot-roostocks came into existence. In the work reported here, attention is
focused on Gisela 5.
Materials and methods. Rootstock trial with ‘Kordia’ and ‘Schneiders Sp. Kn.’
‘Kordia’ and ‘Schneiders Sp. Kn.’ were planted in the planting season of 1995–
1996. The planting distance was 5.00 x 3.00 m (600 trees/ha). The following
rootstocks were used: Colt, Gisela 5, GM61, Limburgse Boskriek (Prunus avium)
and Weiroot 13. For each scion/rootstock combination 2 replication of 5 trees were
planted. Because of their very bad health one replication of ‘Kordia’ on GM61 and
218
both replication of ‘Schneiders Sp. Kn.’ on Weiroot 13 were grubbed. Besides
recording the vigour (trunk circumference and volume), yield and fruit weight were
also determined at harvest.
R e p l a n t p r o b l e m s a n d s o i l s i c k n e s s. In the spring of 1999 on
an old cherry meadow a trial with Colt, Gisela 5 and Limburgse Boskriek (Prunus
Avium) was also started, to look into the sensitivity to soil sickness of each of these
rootstocks. One half of the cherry meadow was disinfected with Formol
(Formaldehyde) and the other half was not. Ten rootstocks were planted each time
between the original positions of the old trees. (The old trees were grubbed and
replaced by young trees.) For a period of 3 years tree vigour and health of the
rootstocks was monitored.
R o o t s t o c k t r i a l w i t h ‘K o r d i a’. ‘Kordia’ was planted in spring 2003.
In the first part of the trial the following dwarfing rootstocks were used: Gisela 5,
PiKu 4.20, Weiroot 158 and Weiroot 53. For each scion/root-stock combination
4 replicates of 2 trees were planted. The planting distance was 5.00 x 2.00 m
(900 trees/ha). In the second part of the trial we used the following rootstocks: Colt,
Gisela 6, MaxMa 14, PiKu 4.20, Weiroot 13 and Weiroot 53. For each scion/rootstock
combination 4 replicates of 1 tree were planted. In this part of the trial the planting
distance was 5.00 x 3.00 m (600 trees/ha). Besides recording the vigour (trunk
circumference and shoot length of the 1-year-old shoots), yield and fruit weight
were also determined at harvest.
Results and discussion. R o o t s t o c k t r i a l w i t h ‘K o r d i a’ a n d
‘S c h n e i d e r s S p. K n.’ In the first years the vigour of Limburgse Boskriek is
weaker than that of Colt. This results from the fact that the trees on Limburgse
Boskriek have more problems to start with growing than the trees on Colt. After 10
growth years the increase in trunk circumference is almost equal for both rootstocks
(Table 1). Weiroot 13 also has a comparable increase in trunk circumference. On
the other hand Gisela 5 grows more slowly.
So far as yields are concerned it appears from table 2 that Gisela 5 and also
Weiroot 13 on ‘Kordia’, gave better results than Colt or Limburgse Boskriek. The
latter two produced almost similar yields. Gisela 5, despite these high yields, also
induced very large individual fruit weights. It produced the same proportions of
dark-red, fully ripe cherries as Colt and Limburgse Boskriek. The same similarities
and comparisons were also noted concerning the percentage of cracked cherries.
R e p l a n t p r o b l e m s a n d s o i l s i c k n e s s. Colt is often used in north
Germany because this rootstock has fewer problems with soil sickness. The results
from the Oregon State University also prove that Colt does better on a plot with soil
sickness than Limburgse Boskriek (Long, 1995). These results were obtained by a
grower, who grew ‘Bing’ grafted on Limburgse Boskriek and Colt on a plot with soil
sickness. The trees on Limburgse Boskriek were small and weak and showed almost
no growth. The trees on Colt on the other hand were vigorous and strong. They also
came into production earlier and moreover produced a bigger yield. The individual
fruit weights were the same for both rootstocks. This experiment also proves that
the first years are al lot more difficult for Limburgse Boskriek, certainly so on a plot
with soil sickness (Vercammen, 2002).
219
T a b l e 1. The increase in trunk circumference of ‘Kordia’ and
‘Schneiders Sp. Kn.’ on different rootstocks (PCF-PPS,
2005a)
1
l e n t e l ë.
‘Kordia’ ir ‘Schneiders Sp. Kn.’ veisliø vaismedþiø su skirtingais
poskiepiais kamienø apimties padidëjimas (PCF-PPS, 2005a)
Increase of trunk circumference
Kamieno apimties padidëjimas
% compared to Limburgse
Boskriek
1996–2005 m., mm
% palyginus su Limburgse Boskriek
‘Kordia’
Limburgse Boskriek
Colt
Weiroot 13
Gisela 5
GM61
60.2
59.3
58.9
51.8
31.7
100
99
98
86
53
‘Schneiders Sp. Kn.’
Limburgse Boskriek
Colt
Gisela 5
GM61
61.3
64.6
56.0
28.9
100
105
91
47
Variety / Rootstock
Veislë / Poskiepis
On the non-disinfected plot no growth could be observed at all on the rootstocks
(Figure 1). In the first year, Gisela 5 did not grow well either on the non-disinfected
plot. Colt on the other hand had the biggest increase in trunk circumference, on the
disinfected plot as well as on the non-disinfected plot. The number of dead rootstocks
was much bigger with Limburgse Boskriek than with Colt or Gisela 5. In conclusion
we can say that Colt knew the best start (Tilkens, 1999).
1
F i g. 1. The increase in trunk circumference of different rootstocks
(PCF-PPS, 2001)
p a v.
Skirtingø poskiepiø kamienø apimties padidëjimas (PCF-PPS, 2001)
220
R o o t s t o c k t r i a l w i t h ‘K o r d i a’ p a r t 1. After 3 growing years
there were no significant differences between the different rootstocks as far as the
increase in trunk circumference is concerned (Figure 2). The smallest increases
however were found with Gisela 5 and Weiroot 158. The first one had also the
shortest shoots in 2005 (Table 2). All rootstocks had the same number of shoots in
2005.
F i g. 2. The increase in trunk circumference of ‘Kordia’ on different rootstocks
(PCF-PPS, 2005a)
2
p a v. ‘Kordia’ veislës vaismedþiø su skirtingais poskiepiais kamienø apimties
padidëjimas (PCF-PPS, 2005a)
T a b l e 2. Yield data concerning ‘Kordia’ and ‘Schneiders Sp. Kn.’ on
different rootstocks (PCF-PPS, 2005b)
2
l e n t e l ë. ‘Kordia’ ir ‘Schneiders Sp. Kn.’ veisliø vaismedþiø su skirtingais
poskiepiais derlius (PCF-PPS, 2005b)
Kg/tree
Variety/ Rootstock
Veislë / Poskiepis
Kg/medis (1999–2005)
Trunk circumference
kg/cm
Kamieno apimtis,
Fruit weight
g
Vaisiaus masë,
Kg/tree / Kg/medis
%
1999–2005
1999–2005
Limburgse Boskriek
57.4
100
0.87
11.2
Colt
68.0
118
1.03
11.2
Weiroot 13
92.0
160
1.38
11.0
Gisela 5
103.2
180
1.80
11.3
GM61
34.3
60
1.02
10.1
Limburgse Boskriek
30.8
100
0.46
11.6
Colt
22.6
73
0.32
11.2
Gisela 5
68.4
222
1.22
11.4
GM61
35.8
116
1.09
10.6
‘Kordia’
‘Schneiders Sp. Kn.’
221
The trees are still too young to draw already conclusions about the yield data.
In 2006 the yield of the trees on Weiroot 158 was lower and the fruit size was
smaller, although these trees started with the same amount of flower buds as trees
on the other rootstocks. The trees on PiKu 4.20 had the highest yield. The fruit
weight was the same as for the trees on Gisela 5 (Table 3).
T a b l e 3. Yield data and shoot length concerning ‘Kordia’ on
different rootstocks (PCF-PPS, 2005c)
3
l e n t e l ë. ‘Kordia’ veislës vaismedþiø su skirtingais poskiepiais derlius ir
ûgliø ilgis (PCF-PPS, 2005c)
Rootstock
Kg/tree
Poskiepis
Kg/medis, 2006
Fruit weight
g, 2006
Vaisiaus masë,
Shoot length
cm, 2005
Ûgliø ilgis,
Trial 1
Gisela 5
2.7 ab
11.3 a
53 b
PiKu 4.20
3.6 a
11.0 a
57 ab
Weiroot 158
2.4 b
11.3 a
56 ab
Weiroot 53
3.0 a
10.5 a
73 a
Colt
2.5 ab
11.2 a
71 a
Gisela 6
4.8 a
10.6 ab
45 b
MaxMa 14
1.3 b
10.3 b
51 ab
PiKu 4.20
4.1 ab
11.5 a
51 ab
Weiroot 13
2.7 ab
11.0 ab
60 ab
Weiroot 53
3.7 ab
11.1 ab
60 ab
Trial 2
R o o t s t o c k t r i a l w i t h ‘K o r d i a’ p a r t 2. In the second part of the
trial the increase of the trunk circumference after 3 growing years is the strongest
for the trees on Colt. These trees had in 2005 also the longest 1-year-old shoots.
The shoot length on Gisela 6 and the number of shoots were significant lower than
on Colt. Also the trees on MaxMa 14 had less shoots than the trees on Colt.
Although it is too early to say much about the yield we want to make a few
remarks. In 2006 trees on Gisela 6 and on PiKu 4.20 had the highest yield. Fruit size
was better on PiKu 4.20 than on Gisela 6. MaxMa 14 on the other hand gave the
lowest yield of all the rootstocks in the trial. In spite of this lower yield, the fruit size
was the smallest on MaxMa 14.
Conclusion. The original aim of this work, to find a rootstock capable of
producing smaller trees, which are easier to control, and suitable for Belgian planting
conditions has been achieved with Gisela 5. Moreover the trees on Gisela 5 come
into production earlier and have the highest yield efficiency, which can shorten the
time between planting and the orchard coming into profit. It is also easier to intensify
plantings and provide protection against birds and rain when using Gisela 5.
222
Gisela 5 is a hybrid between Prunus cerasus and Prunus canescens. It is a
rootstock with moderate to weak vigour (Wertheim, 1998). The yield efficiency of
Gisela 5 is very high, and it induces good fruit sizes on scions. However, under dry
conditions cherries on Gisela 5 can sometimes remain too small. Although this can
be solved quite easily by watering the trees. Just as with the other two rootstocks
Gisela 5 is suitable for most varieties. This rootstock is best suited for intensive
cherry culture. The recommenced planting distances are 5 x 3 m and 4 x 2 m. The
trees reach a height of 3 to 4 meters, which makes the use of bird nets and/or plastic
covers possible. Gisela 5 is less susceptible to soil sickness than Limburgse Boskriek.
Gauta
2006 04 28
Parengta spausdinti
2006 08 07
References
1. L o n g L. Colt rootstock may be answer for replant problems, “Good Fruit
Grower”. 1995. February 15. P. 43–44.
2. P C F - P P S. Annual report “PCF-Proeftuin Pit- en Steenfruit”. 2001. P. 328–330.
3. P C F - P P S. Annual report “PCF-Proeftuin Pit- en Steenfruit”. 2005 a. P. 53–56.
4. P C F - P P S. Annual report “PCF-Proeftuin Pit- en Steenfruit”. 2005 b. P. 59–60.
5. P C F - P P S. Annual report “PCF-Proeftuin Pit- en Steenfruit”. 2005 c. P. 61–62.
6. T i l k e n s N. Is Colt te vroeg afgeschreven? “Fruitteeltnieuws”. 199913(7). P. 6–7.
7. W e r t h e i m S. J. Rootstock Guide. 1998. P.101–105.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
218–223.
GISELA 5 POSKIEPIO NAUDOJIMAS TREÐNËMS
J. Vercammen, G. Van Daele, T. Vanrykel
Santrauka
Atliekant tyrimus su treðnëmis, buvo siekiama rasti toká þemaûgá poskiepá, kaip M.9
obelims, kuris leistø uþauginti ankstyvà derliø duodanèius ir neaukðtus vaismedþius, kad
bûtø galima nuskinti visas treðnes stovint ant þemës. Gisela 5 yra Prunus cerasus ir Prunus
canescens hibridas. Tai vidutinio augumo poskiepis. Gisela 5 – labai produktyvus poskiepis,
sunokina tinkamo dydþio uogas. Kartais, kai orai itin sausi, uogos gali likti pernelyg maþos.
Taèiau ðià problemà galima lengvai iðspræsti vaismedþius laistant. Gisela 5 tinka daugeliui
ðiuolaikiniø veisliø. Ðis poskiepis tinkamiausias treðnes auginant intensyviai. Gisela 5
padëjo pasiekti pradiná tikslà – iðauginti maþesnius, lengviau priþiûrimus vaismedþius. Jie
pradeda duoti derliø anksèiau, todël sodas greièiau gali duoti optimalø pelnà. Be to,
naudojant Gisela 5, treðnës intensyviau auga, jas lengviau pridengti nuo lietaus ir paukðèiø.
Reikðminiai þodþiai: þemaûgis poskiepis, Gisela 5, dirvos ligotumas.
223
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 224–229.
THE EFFECT OF ROOTSTOCK ON GROWTH AND
FRUITAGE OF SWEET CHERRY
Zofia TOMASZEWSKA, Bartosz NYCHNEREWICZ
Department of Horticulture, University of Warmia and Mazury in Olsztyn.
E-mail: [email protected]
An experiment was conducted in 2003–2005 aimed at examining the effect of rootstocks
Prunus avium, Colt, PHL A and Gisela 5 on growth and fruitage of the following cultivars
of cherry trees: ‘Burlat’, ‘Kordia’, ‘Regina’ and ‘Van’. Dwarf rootstocks PHL A and Gisela
5 reduced tree growth by about 40–45% as compared with rootstocks Colt and Prunus
avium. The yielding of sweet cherry trees on these rootstocks was much better. The best
yielding was observed in case of cultivar ‘Van’. During the experiment, there were found
physiological incompatibilities between cultivar ‘Burlat’ and rootstock PHL A, as well as
between cultivar ‘Van’ and rootstock Colt.
Key words: rootstock, sweet cherry, growth, yielding.
Introduction. Intensively growing seedling rootstock Prunus avium L. and
clonal rootstocks F12/1 and Colt are prevalent in the cultivation of sweet cherries.
Modern, cost-effective cultivation should be carried out on dwarf trees, in the same
way as the intense cultivation of apple trees (Sitarek, 2004). For some years, great
progress has been observed in the world in the cultivation of weak-growing rootstocks
(Cheùpiñski, 2000; Larsen et al., 1997; Moreno et al., 1995; Rozpara, 2001). Its
usage makes it possible to weaken the growth, and in consequence, to increase the
number of trees growing on a given unit of area. Also, tree crowns are easier to
form, fruit is protected against cracking by using a plastic tunnel, and protection
against birds is easier. Research concerning weak-growing rootstocks has been
conducted since 1988 at the Research Institute of Pomology. It has been proven that
it is valuable for cherry fruit producers to use new technologies (Grzyb, 1999; Sitarek
and Buczek, 2005). This study presents the results of the assessment and comparison
of Czech rootstock PHL-A and German rootstock Gisela 5 against rootstocks Colt
and Prunus avium that had been used so far.
Materials and methods. The research was conducted in Úwiedziebnia next to
Brodnica. The orchard was established in the autumn of 1999 from branched shoots
of budded plants on brown soil of proper typical III class. Trees were bought in
Werfelden in Germany. Cultivars ‘Kordia’ and ‘Regina’ were grown on rootstocks
Gisela 5 and PHL-A, planted 2.5 x 4.0 m apart (1000 trees/ha), while cultivars ‘Burlat’
224
and ‘Van’ were planted 3.0 x 4.0 m apart (833 trees/ha). On the other hand, trees on
strongly growing rootstocks Colt and Prunus avium (own cultivation) were grown
3.5 x 4.0 m apart (714 trees/ha). From 2000 to 2004, trees on rootstocks PHL and
Gisela 5 were grown with stakes. Measurements of the height and yield were taken
from 20 trees. Crown volume at random heights was counted. The interrows of
trees contained turf. However, in the rows, in the first three years, mulching by bark
was used, and after 2003 herbicide fallow was used. The research lasted for three
years (2003–2005) under various climatic conditions. Data statistically was processed
by a computer program ANOVA for EXEL vers.2.1.
F i g. 1. Total precipitation in 2003–2005
1
p a v. Bendras krituliø kiekis 2003–2005 m.
F i g. 2. Average temperatures in 2003–2005
2
p a v. Vidutinës temperatûros 2003–2005 m.
Results. Assuming the area of the trunk cross-section as a criterion of growth
strength, it was established that this feature depended on rootstock and cultivar.
Trees on rootstock Prunus avium grew more strongly than the others. Trees on
rootstock PHL A. grew most poorly. Rootstock Gisela 5 demonstrated the largest
growth strength. It must be emphasized that trees on this rootstock for the first four
225
years grew quite strongly – the increments of the surface area were similar to
rootstock Colt (Table 1), and only in fifth and sixth year of the experiment their
growth was weaker.
T a b l e 1. Surface trunk cross-section area (TCSA), cm2 and crown
volume, m3
1
l e n t e l ë. Kamieno skerspjûvio plotas (KSP), cm2 ir vainiko tûris, cm3
Prunus avium
Cultivars
Veislës
‘Burlat’
Years
Metai
1
2
3
average
TCSA
crown
volume
Colt
PHL A
crown
volume
TCSA
TCSA
crown
volume
Gisela-5
TCSA
crown
volume
KSP
vainiko
tûris
KSP
vainiko
tûris
KSP
vainiko
tûris
KSP
vainiko
tûris
59.95
108.81
147.67
105.47
8.8
8.9
10.9
9.5
46.20
97.50
138.80
94.16
8.0
7.3
8.1
7.8
19.55
31.00
-*
4.0
4.4
-*
40.55
87.92
108.13
78.9
7.4
7.0
5.2
6.5
45.94
90.65
130.36
88.98
7.9
7.7
8.7
8.1
44.98
85.34
103.90
78.07
6.0
6.8
5.8
6.2
24.96
48.42
80.00
51.12
3.0
3.5
3.6
3.4
30.84
60.53
74.36
55.24
6.0
6.7
4.8
5.8
59.93
94.50
126.16
93.53
6.2
7.6
7.9
7.2
37.50
70.32
98.66
68.82
4.0
3.8
4.3
4.0
29.50
9.94
82.40
53.95
3.6
3.4
3.5
3.5
28.90
61.50
76.10
55.50
4.2
3.6
3.9
3.9
48.99
90.99
135.93
91.97
9.5
9.0
10.9
9.8
16.06
-*
-*
3.3
-*
-*
25.90
58.44
96.80
67.04
4.4
5.8
6.4
5.5
43.64
62.92
79.33
61.96
6.8
6.6
6.0
6.5
vidurkis
‘Kordia’
1
2
3
average
vidurkis
‘Regina’
1
2
3
average
vidurkis
‘Van’
1
2
3
average
vidurkis
LSD05 / R05 Trunk cross section: cultivars – 16.207, years – 10.579, rootstock – 14.511
Kamieno skersmuo priklausomai nuo: veislës – 16,207, metø – 10,579, poskiepio – 14,511
Crown volume: cultivars – 3.756, years – n.o, rootstock – 3.735
Vainiko tûris priklausomai nuo: veislës – 3,756, metø – n.s, poskiepio – 3,735
*physiological incompatibility 1 – 2003, 2 – 2004, 3 – 2005 / fiziologinis nesuderinamumas:
1 – 2003 m., 2 – 2004 m., 3 – 2005 m.
During six years, the largest dimensions were obtained by cultivar ‘Burlat’ on
rootstock Prunus avium. The weakest growth was found for cultivar ‘Regina’ on
rootstock PHL A. During the experiment, a weaker growth followed by drying-up of
trees of cultivar ‘Van’ on rootstock Colt and cultivar ‘Burlat’ on rootstock ‘PHL A’
was observed. Both examined rootstocks, PHL A and Gisera-5, weakened the growth
of trees in comparison to rootstock Colt on average by 27% and to rootstock Prunus
avium by 40%. On the basis of the average values obtained for rootstocks and
cultivars, it was established that the strongest growth was characteristic to cultivars
‘Burlat’ and ‘Van’ and the weakest was of ‘Kordia’.
Trees growing on rootstocks Prunus avium and Colt had much bigger tree
226
crowns. Rootstock PHL A largely reduced the volume of crowns. On the other hand,
trees grown on rootstock Gisela 5 had slightly smaller crowns than those growing
on rootstock Colt.
In the final year of investigation, the crown volumes of cultivars ‘Kordia’ and
‘Burlat’ were smaller on this rootstock than in the previous year. There were
differences observed between cultivars. ‘Burlat’ and ‘Van’ had much larger crowns
than cultivars ‘Regina’ and ‘Kordia’.
The fruitage of sweet cherry trees in individual years was differentiated because
of climatic conditions. Good yielding was observed in 2004. Small yields in the
subsequent year were caused by spring frosts (on May 05, 2005, the temperature at
night dropped down to -5°C) and some flowers froze. Sweet cherry trees of cultivar
‘Van’ yielded the best, and those of cultivar ‘Regina’ demonstrated the poorest yielding.
The results obtained indicated that the type of rootstock diversified yielding.
Definitely, Gisela 5 and PHL A proved to be better. Much smaller yields were obtained
on rootstocks Colt and Prunus avium.
T a b l e 2. Yielding of sweet cherry trees depending on rootstock
2
l e n t e l ë. Treðniø derliaus priklausomumas nuo poskiepio
Rootstocks / Poskiepiai
Cultivars
Veislës
Years
Metai
Prunus avium
kg·tree-1
kg·vaism.-1
-1
t·ha
Colt
kg·tree-1
kg·vaism -1
PHL A
-1
t·ha
kg·tree-1
kg·vaism -1
Gisela-5
-1
t·ha
kg·tree-1
kg·vaism -1
t·ha-1
‘Burlat’
1
2
3
Ó
2.60
17.90
3.66
24.15
1.85
12.78
2.61
2.22
8.90
4.93
16.05
1.58
6.35
3.52
0.60
1.22
-*
1.82
0.49
1.02
7.00
14.95
6.20
27.69
5.83
12.45
5.16
‘Kordia’
1
2
3
Ó
4.5
6.43
2.83
13.74
3.21
4.59
2.02
7.8
8.25
3.80
19.86
5.57
5.91
2.71
5.85
12.32
5.73
23.88
5.57
12.32
5.73
9.95
13.93
7.43
31.29
9.95
13.93
7.43
‘Regina’
1
2
3
Ó
3.2
9.0
1.56
13.74
2.28
6.43
1.11
5.2
8.25
2.93
16.38
3.71
5.89
2.09
8.50
10.25
4.30
23.04
8.50
10.25
4.30
10.03
12.35
5.50
27.87
10.03
12.35
5.50
‘Van’
1
2
3
Ó
8.33
12.22
10.62
31.17
5.94
8.72
7.58
1.11
-*
-*
0.79
8.70
13.35
15.0
37.05
7.25
11.12
12.49
12.33
10.0
15.20
37.53
10.27
8.33
12.66
LSD05/R05 kg·tree-1: cultivars – 2.063, years – 1.687, rootstock – 1.919
Derlius kg vaism.-1 priklausomai nuo: veislës – 2,063, metø – 1,687, poskiepio – 1,687
t·ha-1: cultivars – 1.820, years – 1.460, rootstock – 1.662
-1
Derlius t·ha priklausomai nuo: veislës – 1,820, metø – 1,460, poskiepio – 1,662
*physiological incompatibility 1 – 2003, 2 – 2004, 3 – 2005 / fiziologinis nesuderinamumas:
1 – 2003 m., 2 – 2004 m., 3 – 2005 m.
It must be emphasized that one of the factors that limited yielding was the
occurrence of physiological incompatibility in trees with cultivar ‘Van’ on rootstock
Colt and cultivar ‘Burlat’ on rootstock PHL A.
227
Total yield per 1 cm2 of trunk cross section resulted in this diversification of
productivity rate for the cultivars under examination. Taking into consideration the
average surface area of the trunk (PPPP) and the average total yield obtained, it can
be stated that the average productivity rate was found for cultivars ‘Van’
(0.64kg/cm2) and ‘Kordia’ (0.61 kg/cm2), grown on rootstock Gisela 5. The strong
growth of trees and weak yielding resulted in diminishing the productivity rate of
cultivars ‘Kordia’ (0.15 kg/cm2) and ‘Regina’ (0.15 kg/cm2), grown on rootstocks
Prunus avium.
On the basis of the results obtained, it has been established that dwarf rootstocks
had a much greater productivity rate than strong growing ones.
Discussion. Many studies concerning the growth of sweet cherry tree on
rootstock of Czech and German cultivation demonstrated significant weakening of
tree growth (Grzyb, 1999; Rozpara, 2001). The results obtained also indicate a slight
differentiation of growth between rootstocks PHL A and Gisela 5. The physiological
incompatibility between cultivar ‘Van’ and rootstock Colt was evident. However, in
the research conducted by Moreno et al. (1996), Perry (1987) and Rozpara (1999),
the observed health of this cultivar was good and no external symptoms of
physiological incompatibilities with rootstock Colt were observed. It confirms shaky
properties of this rootstock.
Rootstocks PHL-5 used in the experiment limited the growth of the examined
cultivars by about 40–45% in comparison with rootstocks Prunus avium and Colt.
The smallest trees were found in case of cultivar ‘Kordia’.
During the experiment, in 2005, there was a drying-up of trees ‘Burlat’ grafted
on rootstock PHL A when herbicides were started to be used in the rows between
trees. According to Rozpara (2001), the reason for trees dying-off could be the
sensitivity of rootstocks PHL to herbicides.
Higher growth measured by the surface area of the trunk was observed for
sweet cherry trees grafted on Gisela 5 in the first period of research, and then the
growth of trunks and volume of tree crowns increased much more slowly. These
types of dependencies were noted by Grzyb (1999). Gisela rootstocks grew more
strongly up to fourth year and then their growth slowed down.
Yielding was better on dwarf rootstock in the first period of the investigation,
then it was similar.
Due to numerous factors determining yielding, it is difficult to establish explicitly
the effects of the rootstock. According to the data obtained, Colt demonstrated better
yielding than Gisela 5. A favourable effect of rootstock Prunus avium was demonstrated
also by Rozpara (1999), in the case of older trees. An important factor is the resistance
of the rootstock to freezing, as has been demonstrated by the conducted investigation.
The results obtained indicate that rootstock Gisela 5 proved to be the most resistant
to low temperatures, as in 2005, when a strong frost occurred, damage to young
branches wasn’t significant and the yielding of the examined cultivars was the highest.
This supports the results obtained by Grzyb (1999) and Rozpara (1999). The
differentiation of yielding was found in relation to the rootstock and also to the
cultivar. Cultivar ‘Van’ was found to be the most productive. Similar results were
obtained by Perry (1987) and Rozpara (1999)
228
Conclusions. 1. Rootstocks PHL A and Gisela 5 largely weaken the growth of
sweet cherry trees in comparison to rootstocks Colt and Prunus avium.
2. Yielding depended on the used rootstock. The best yielding was found in the
case of rootstock Gisela 5, slightly lower – of PHL A, and the poorest of Prunus
avium, although trees on this rootstock grew most strongly.
3. The most productive was cultivar ‘Van’; the least amount of fruit was
observed in ‘Regina’.
Gauta
2006 05 24
Parengta spausdinti
2006 07 24
References
1. C h e ù p i ñ s k i C. Characteristics of growth strength in three-year-old sweet
cherry trees on PHL series rootstocks. Scientific Journal of the Institute of Pomology and
Floriculture in Skierniewice. 2000. Vol. 8. P. 165–169.
2. G r z y b Z. S. Role of rootstocks and interstock in regulating growth and
fruiting of sweet cherry trees. Symposium: New technologies in pomology in the last
years of the 20th century. Scientific Journal. Kraków, 1999. Issue 8. P. 7–11.
3. L a r s e n F. E., H i g g i n s S. S., F r i t t s R. Scion /interstock/
rootstock effect on sweet cherry yield, tree size and yield efficiency. Scientia. Horticulturae.
1987. Vol. 35. P. 237–247.
4. M o r e n o M. A., T a b u e n c a M. C., C a m b r a R. Adara, a plum
rootstock for cherries and other stone fruit species. Hort Science. 1995. Vol. 30(6). P. 1316–1317.
5. P e r r y R. I. Cherry rootstock In. R. C. Rom and R. F. Carlson (Editors),
Rootstock for Fruit Crops. John Wiley. New York, 1987. P. 217–246.
6. R o z p a r a E. Modern cultivation of cherries. Warszawa, Hortpress, 1999.
P. 6–183.
7. R o z p a r a E. P-HL A. Valuable rootstock for sweet cherry trees. Arboriculture.
2001. 4. P. 16–22.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
224–229.
POSKIEPIØ ÁTAKA TREÐNIØ AUGIMUI IR DERËJIMUI
Z. Tomaszewska, B. Nychnerewicz
Santrauka
2003–2005 metais atliktas bandymas, siekiant iðtirti Prunus avium, Colt, PHL A ir
Gisela 5 poskiepiø átakà ‘Burlat’, ‘Kordia’, ‘Regina’ ir ‘Van’ veisliø treðniø augimui ir
derëjimui. Þemaûgiai poskiepiai PHL A ir Gisela 5 sumaþino vaismedþio augimà maþdaug
40–45%, palyginti su poskiepiais Colt ir Prunus avium. ðie poskiepiai iðaugino daug didesná
derliø. Gausiausià derliø davë ‘Van’ veislë. Bandymo rezultatai parodë fiziologiná ‘Burlat’
veislës ir PHL A poskiepio bei ‘Van’ veislës ir Colt poskiepio nesuderinamumà.
Reikðminiai þodþiai: poskiepis, treðnës, augimas, derlius.
229
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 230–234.
THE EVALUATION OF PLUM TREE CULTIVARROOTSTOCK COMBINATIONS UNDER CONDITIONS
OF SOUTH RUSSIA
Ludmila RYASANOVA, Vasiliy OSTAPENKO
Kuban State Agricultural University, Kalinin str. 13, 350044, Krasnodar,
Russia. E-mail: [email protected]
Comprehensive evaluation of plum cultivars ‘Stenly’ and ‘Kabardinskaya Early’ grafted
on clone rootstocks semi-dwarf AP-1 and dwarf Evrika was given. Myrabalan cherry plum
seedlings served as control. The orchard was planted in 1997, according to scheme
6 x 4 m.
Investigation of plum cultivar-rootstock combinations was carried out in 2000–2005
under conditions of field experiment, laid on leached chernozems of South Russia.
The results obtained show that the studied rootstocks influence greatly the biological
properties and production indices of plum cultivars grafted on them. So on rootstock
AP-1, which is characterized by high drought resistance, the yielding capacity was
10–20% higher than in the control, irrespective of plum cultivar. Evrika influenced positively
only cultivar ‘Kabardinskaya Early’. It was proved experimentally, that clone rootstocks
(AP-1 and Evrika) caused higher accumulation of P-active substances in fruits (vitamin P
and â–carotene).
Key words: plum tree, cultivar, rootstock, productivity, biological indices.
Introduction. Plum is the most common crop in Krasnodar territory. It occupies
up to 8% of all orchards (about 4000 hectares). However, it should be noticed that
the assortment of cultivars grown here are insufficiently drought resistant, having at
the same time high indices of productivity and quality of fruit (Åðåìèí, 2003). As
it is known, the yielding ability of fruit crops in this region is very often determined
by the level of air and soil drought. The selection of cultivar-rootstock combinations
of plum resistant to the unfavourable factor may be the solution of the problem.
Planting highly productive orchards the role of cultivar is difficult to overestimate.
Rootstock is not less important – according to Michurin, it serves as the foundation
of a fruit tree. Researchers’ data both in our country (Êîðíåâà, 1989) and abroad
proved that by selection of cultivars one can achieve increasing of orchard productivity
by 1.5-2 times, and by selection of rootstock it is possible to achieve increasing of
yield of the same cultivar by 2-2.5 times (Watkins, 1976; Webster, 1980).
The possibility of increasing orchard productivity is especially great when using
vegetative propagated clone rootstocks. In the opinion of many authors (Ãðÿçåâ,
230
1999; Êîðíåâà, 1989), these rootstocks allow to form trees with well-known
biological properties (drought resistance, winterhardiness, early ripening) and
production indices (longevity, yielding ability, tree height). All this is important when
selecting rootstock-cultivar combinations, first of all for areas with extreme growth
conditions. As it was mentioned, water is a limiting factor for southern region,
therefore one of the ways to increase productivity of plum planting will be selection
of drought-resistant rootstock. Taking into consideration all that was said, the aim of
our research was to estimate the rootstock-cultivar combinations of plum under
conditions of Prikubanskaya zone of horticulture.
Material and methods. The studies were carried out in 2000–2005 under
conditions of field experiment, laid on leached chernozems of Prikubanskaya zone
of horticulture (South Russia). The objects of investigation were plum tree cultivars
‘Kabardinskaya Early’ and ‘Stenly’ grafted on vegetative propagated rootstocks: semidwarf AP-1 and dwarf Evrika. Myrabalan plum seedlings on stock were used as
control. The orchard was planted in 1997, the scheme of planting was 6 x 4 m. The
methods of accounting and observation were generally accepted (Ïðîãðàììà è
ìåòîäèêà, 1999). Drought resistance was estimated by Kushnirenko’s method
(Êóøíèðåíêî, Êóð÷àòîâà, 1984).
Results. As the analysis of the obtained data showed (Table 1) the average
yield per tree of four years of fruiting on rootstock AP-1, irrespective of the cultivar,
was 25% higher as compared with trees, grafted on Myrabalan plum seedlings.
On rootstock Evrika the yield of cultivar ‘Stenly’ didn’t differ from the control,
while cultivar ‘Kabardinskaya Early’ exceeded it by 9%.
T a b l e 1. The yield of plum tree depending on rootstock (kg/tree)
1
l e n t e l ë.
Slyvø derliaus priklausomumas nuo poskiepio, kg/vaism.
Years / Metai
Average for
2000–2005
Rootstock
Poskiepis
2001
2002
2003
2004∗
2005
2000–2005 m.
vidurkiai
‘Stenly’
Prunus cerasifera
22.1
30.2
42.3
-
40.2
33.7
AP-1
26.4
37.1
56.2
-
50.8
42.6
Evrika
15.0
29.3
45.3
-
43.1
33.2
LSD05 / R05
3.1
1.8
2.7
Prunus cerasifera
7.4
25.5
33.2
-
34.5
25.2
AP-1
9.0
32.0
44.7
-
40.3
31.5
Evrika
7.9
26.1
39.2
-
37.7
27.7
LSD05 / R05
0.8
1.7
3.4
2.2
‘Kabardinskaya Early’
* No yield due to freezing of flower buds in spring.
* Dël pumpurø nuðalimo pavasará derliaus nebuvo.
231
1.5
Investigations showed that under extreme conditions of 2001, 2003 and 2005
hydrothermal index during vegetation stage was correspondingly 0.9; 1.0; 0.9, that
is by 10–19% lower than multiannual average. Plum cultivars showed rather high
resistance to drought only on rootstock AP-1 (Table 2).
T a b l e 2. Estimation of drought resistance of plum cultivars on
different rootstocks, ERLT* (%)
2
l e n t e l ë.
Rootstock
Poskiepis
Prunus cerasifera
AP-1
Evrika
LSD05 / R05
Slyvø veisliø su skirtingais poskiepiais atsparumo sausrai
ávertinimas, LAV*, %
‘Stenly’
2001
2003
10.3
8.5
7.5
5.3
14.0
7.9
2.4
1.7
2005
9.6
6.4
10.2
2.1
‘Kabardinskaya Early’
2001
2003
2005
9.7
7.9
8.5
7.1
4.7
5.9
11.4
8.1
9.6
0.9
1.5
2.3
* electric resistance of leaf tissues / lapo audiniø varþa
The experiment showed that productivity and chemical composition of plum
tree cultivars changed under the influence of rootstock. This influence was less for
cultivar ‘Kabardinskaya Early’, than for ‘Stenly’. Thus, cultivar ‘Stenly’ on clone
rootstocks accumulated 5–9% more dry matters and sugars, while in cultivar
‘Kabardinskaya Early’ these indices didn’t change. It should be stressed that
combinations with clone rootstocks, regardless of the cultivar, differ in higher quantity
of biologically active substances. For example, the content of vitamin P in fruits of
the studied cultivars when using rootstock AP-1 was higher by 3–9% and on rootstock
Evrika – by 13–20% compared with seed rootstock. The content of b-carotene in
plum fruit appeared to be 4–13% higher on rootstock AP-1 and by 5–9% on rootstock
Evrika.
The predominance of vitamin C is marked in fruits of control. Thus, when
using seed rootstocks this index in cultivar ‘Stenly’ is 26% higher, and in cultivar
‘Kabardinskaya Early’ is 16% higher in comparison with clone rootstocks. When
using clone rootstocks in fruit cultivar ‘Stenly’ the amount of pectin substances
depend on rootstock, in fruit ‘Kabardinskaya Early’ this parameter does not change
under the influence of rootstock (Table 3).
Discussion. The influence of rootstock on different characteristics of cultivar
is generally known. The most significant of them is yielding; even the character of
frutification is in genetically stipulated limits. The essential changes occur under the
influence of rootstock in metabolisms of fruit plants, that’s why the rootstock is the
most available and active means regulating not only growth vigour and productivity
of grafted cultivar, but also separate indices of fruit product quality (Êóäðÿâåö,
1987).
According to our data, the productivity of plum trees to a great extent depends
on hardiness of rootstocks to drought. The higher yielding of studied cultivars,
especially on drought-resistant rootstock AP-1, witnesses about it.
232
T a b l e 3. Biochemical indices of plum fruit (average of 2003, 2005)
3
l e n t e l ë.
Rootstock
Poskiepis
Slyvø vaisiø biocheminiai rodikliai, 2003, 2005 m. vidurkiai
Dry soluble
solids
Tirpios sausosios medžiagos,
Amount of
sugars
Cukrûs, %
Total acidity
Bendras rûgštumas, %
%
Vitamins
Vitaminai,
mg 100 g
β-carotene
â-karotinas,
mg 100 g
Amount
of
pectins
Pektinai,
%
Ñ
Ð
3.5
60.4
0.44
0.66
‘Stenly’
Prunus
cerasifera
13.3
9.7
0.45
AP-1
14.5
10.6
0.36
2.6
62.0
0.50
0.64
Evrika
14.0
10.2
0.41
2.5
66.6
0.46
0.36
LSD05/R05
0.5
-
-
0.8
1.7
0.2
-
3.3
71.0
0.53
0.37
‘Kabardinskaya Early’
Prunus
cerasifera
12.1
8.8
0.82
AP-1
12.5
8.4
0.73
2.8
78.0
0.60
0.37
Evrika
12.5
8.9
0.92
3.0
85.8
0.57
0.37
F05 > FÔ
-
-
0.2
3.1
0.05
-
LSD05/R05
Due to the used materials, biochemical content of fruit, determining gustatory,
food and curative-preventive qualities, is changed in dependence on biological
peculiarities not only of cultivar, but of rootstock as well. This opportunity isn’t
used in full extent for formation of separate indices of fruit quality.
According to some researchers (Ëåâãåðîâà, 1997; Êàñüÿíîâ, 2001), when
evaluating food peculiarities of cultivars, the content of dry soluble solids in fruit has
a great significance. Increase of this index even by 1% significantly influences the
process of obtaining of different fruit products. According to our results we can
retrace some tendency in the change of chemical fruit content, occurring under the
influence of rootstock. The weaker is intensity of used rootstock growth, the higher
is content of dry and P-active substances and the lower is vitamin C and pectins in
fruits.
Thus, the proper selection of cultivar-rootstock combinations can provide not
only stable fruit bearing of plum, but also formation of fruits with given properties.
Conclusion. New rootstocks AP-1 and Evrika (selection of Krimskiy
experimental-selection station All-Russia Institute of Plant Production) show high
degree of adaptation to specific weather conditions of the region what allows to
raise productivity of the studied plum cultivars by 10–20%. The utilization of these
rootstocks causes the increasing of the content of dry soluble solids and P-active
substances.
Gauta
2006 04 06
Parengta spausdinti
2006 07 13
233
References
1. W a t k i n s R. Fruit Breeding. Apple Rootstock. Ann Rep. (East Malling Res.
St.). 1975. Kent. P. 97-98.
2. W e b s t e r A. D. Dwarfing Rootstocks for Plums and Cherries Reprint.
Symposium “Plant and Orchard Systems”. Italy. Lana. August 3-8, 1980.
3. Ã ð ÿ ç å â Â. Âûðàùèâàíèå ñàæåíöåâ äëÿ âûñîêîïðîäóêòèâíûõ
ñàäîâ. Ñòàâðîïîëü, 1999. Ñ. 60–99.
4 Å ð å ì è í Ã. Â. Ñëèâà è àëû÷à. Õàðüêîâ «Ôîëèî», 2003. 302 ñ.
5. Ê à ñ ü ÿ í î â Ã. È., Ë î ì à ÷ è í ñ ê è é Â. À., Ñ à ì ñ î í î â à À.
Í. Òåõíîëîãèÿ ïðîäóêòîâ äëÿ äåòñêîãî ïèòàíèÿ. Ðîñòîâ í/Ä, 2001. 259 ñ.
6. Ê î ð í å â à Í. È. Ðîñò è ïëîäîíîøåíèå ìîëîäûõ äåðåâüåâ â
çàâèñèìîñòè îò ïîäâîÿ, ñîðòà è ðåæèìà ïèòàíèÿ â ÿáëîíåâîì ñàäó //
Ïëîäîâîäñòâî. 1989 . Âûï.7. Ñ. 79-84.
7. Ê ó ø í è ð å í ê î Ì. Ä., Ê ó ð ÷ à ò î â à Ð. Ï. Ìåòîäû äèàãíîñòèêè
çàñóõîóñòîé÷èâîñòè è æàðîóñòîé÷èâîñòè
ïëîäîâûõ êóëüòóð //
Ôèçèîëîãè÷åñêèå îñíîâû àäàïòàöèè ìíîãîëåòíèõ êóëüòóð ê
íåáëàãîïðèÿòíûì ôàêòîðàì ñðåäû .Êèøèíåâ, 1984. Ñ. 241-245.
8. Ê ó ä ð ÿ â å ö Ð. Ï. Ïðîäóêòèâíîñòü ÿáëîíè. Ì.: Àãðîïðîìèçäàò,
1987. 303 ñ.
9. Ëåâãåðîâà Í. Ñ., Ñåäîâ Å. Å, Ñåäîâà Ç. Ì. Èñïîëüçîâàíèå ïëîäîâ
èììóííûõ è óñòîé÷èâûõ ê ïàðøå ñîðòîâ è ãèáðèäíûõ ôîðì ÿáëîíè
äëÿ ïðîèçâîäñòâà ñîêîâ / Õðàíåíèå è ïåðåðàáîòêà ñåëüõîçñûðüÿ. 1997.
Ñ. 37-38.
10. Ï ð î ã ð à ì ì à è ìåòîäèêà ñåëåêöèè ïëîäîâûõ, ÿãîäíûõ è
îðåõîïëîäíûõ êóëüòóð. Îðåë, 1999. 502 ñ .
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
230–234.
SLYVØ VEISLIØ IR POSKIEPIØ DERINIØ ÁVERTINIMAS PIETØ RUSIJOS
SÀLYGOMIS
L. Riazanova, V. Ostapenko
Santrauka
Pateiktas iðsamus ‘Stenly’ ir ‘Kabardinskaya Early’ veisliø slyvø su vegetatyviniais
pusiau þemaûgiais (AP-1) ir þemaûgiais (Evrika) poskiepiais ávertinimas. Myrabalan sëjinukai
buvo kontrolinis variantas. Sodas buvo pasodintas 1997 m. pagal schemà
6 x 4 m.
Slyvø veisliø ir poskiepiø deriniø tyrimas buvo atliktas 2000–2005 m. lauko bandymo,
árengto iðplautame juodþemyje Pietø Rusijoje, sàlygomis.
Gauti rezultatai rodo, kad tirti poskiepiai darë didelæ átakà á juos áskiepytø slyvø
veisliø biologinëms savybës ir produkcijos rodikliams. Slyvø su labai atspariu sausrai
poskiepiu AP-1 derlingumas buvo 10–20% didesnis negu kontrolinio varianto,
nepriklausomai nuo slyvø veislës. Evrika teigiamai veikë tik ‘Kabardinskaya Early’ veislæ.
Bandymais árodyta, kad vegetatyviniai poskiepiai (AP-1 ir Evrika) lëmë didesná P-aktyviø
medþiagø susikaupimà vaisiuose (vitamino P ir ■karotino).
Reikðminiai þodþiai: slyvos, veislës, poskiepiai, derlingumas, biologiniai rodikliai.
234
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 235–242.
GROWTH, YIELDING AND FRUIT QUALITY OF PLUM
CULTIVAR ‘ÈAÈANSKA NAJBOLIA’ DEPENDING ON
THE USED INTERSTOCKS
Ewa DZIEDZIC, Monika MAÙODOBRY, Wùodzimierz LECH
Agricultural University, Pomology and Apiculture Department, 31-425
Kraków, al. 29 Listopada 54, Poland. E-mail: [email protected]
The experiment was set up in spring of 1998, at experimental station located near
Krakow. The trees were obtained by grafting 30 cm length interstems of Isthara, Sanctus
Hubertus, Wangenheim Prune, Early Prune, GF 655/2 on the rootstock of Wangenheim
Prune. The trees were planted at a spacing of 4 x 2 m. The objective of the studies was to
determine the influence of interstems on tree size reduction expressed as TCSA, marketable
yield, efficiency index, fruit mass, fruit juice content of plum ‘Èaèanska Najbolia’. The
observations and measurements carried out in 2001–2005 evidenced that interstems
reduced the plum trees size.
Key words: ‘Èaèanska Najbolia’, growth reduction, interstems, plum.
Introduction. Reduction of tree growth by appliance of interstem depends on
growth vigour and length of interstem. The advantageous of interstem are: reduction
of tree growth (Mielke, Turner, 2002), better fruiting, bigger fruit mass and greater
productivity coefficient (Filho et al., 2000), well coloured fruit, great usefulness of
trees for planting on the light soils. The interstems can be also applied at the case of
incompatibility between rootstock and grafted cultivar (Rodrigez, Castro, 2002).
There are also reports about the interstocks affect on mineral content in the leaves
(Rozpara et al., 1990; Milosevic, 2006). Often the effect of used interstems depends
on the length of interstem. Czynczyk (2002) using the interstems of P 22 rootstock
(20-30 cm in length) for cvs. ‘Gloster’ and ‘Melrose’ growing on Antonovka rootstock
obtained the greater reduction of trees growth and higher productivity for the trees
with longer interstems. Whereas Wertheim and Callessen (2000) using the interstems
of cvs. ‘Gloster’ and ‘Golden Delicious’ for ‘Elstar’ and ‘Jonagold’ growing on M.9
rootstock found that the interstems affected the trees growth, but not the index of
productivity. Sometimes even the microinterstocks (2 cm in length) can be used for
growth reduction (Poniedziaùek, 1995). The interstems are widely used for sweet
cherries (Grzyb et al., 1985; Rozpara, Grzyb, 2004, Rozpara et al., 2004) reducing
tree growth, increasing yield, frost resistance enabling precocity. There are few
reports about interstocks for plum trees (Grzyb, Rozpara, 1993, Grzyb, Rozpara,
1994; Duriã et al., 1997).
235
The aim of the studies was to show the possibility of tree growth reduction and
presentation of high productivity coefficient for ‘Èaèanska Najbolia’ plum cultivar at
the appliance of five interstocks.
Material and methods. The trees were planted in the spring of 1998, at a
distance of 4m x 2m. The growing cultivar was ‘Èaèanska Najbolia’ on
WangenheimPrune rootstock. The interstems of Isthara, Sanctus Hubertus,
Wangenheim Prune, Early Prune and GF 655/2 (15 cm in length) were investigated.
The pollinator in the orchard was ‘Èaèanska Lepotica’. The experiment was set up
in four replications, with 5 trees in each experimental plot. The following observations
and measurements were carried out in 2001–2005: marketable yield, mass of 100
fruit, trunk cross sectional area (TCSA), index of productivity, total soluble solids
(TSS), titratable acidity (TA). Soluble solids content and titratable acidity were
measured according to Polish Standards. Soluble solids content was measured in
excised juice using a digital temperature – compensated refractometer (model
PR-101, Atago, Japan). Titratable acidity expressed as malic acid, was determined
by a filtration of dilute sample of extract of macerated fruit tissue with 0.1 n NaOH
to pH 8.1.
During the years 1998–2005 temperature and precipitation were measured and
the values are presented in Table 1.
T a b l e 1. Total precipitation and mean year temperature in 1998–
2005 and multiannual average.
1
l e n t e l ë. Bendras krituliø kiekis, vidutinë metinë temperatûra 1998–2005 m.
ir daugiameèiai vidurkiai
1998 1999 2000 2001 2002 2003 2004 2005
Total year precipitation
Bendras metinis krituliø kiekis, mm
Multiannual mean precipitation
Daugiametis vidutinis krituliø kiekis, mm
Mean year temperature
Vidutinë metinë temperatûra, °C
Multiannual mean temperature
Daugiametë vidutinë temperatûra, °C
669.9 634.3 689.2 865.2 568.3 568.1 556.2 604.2
641.9
9.7
10.1
8.8
7.8
8.7
7.8
7.8
7.9
8.8
Total precipitation in years 1998–2000 was approximated to many years’ mean,
in year 2001 exceeded that mean, while in year 2002 and 2005 total precipitation was
lower than that mean. Many years’ mean temperature was 8,8oC, in year 2000 and
2002 the temperature was similar to that value, in year 1998 and 1999 mean year
temperature was higher than that mean, in other years mean year temperature was
lower than many years’ mean.
Results. The results concerning marketable yield of plum trees ‘Èaèanska
Najbolia’ in 2000–2005 (1st to 5th year of fruiting) were presented in Table 2.
236
T a b l e 2. Marketable yield of plum trees ‘Èaèanska Najbolia’
depending on applied interstem (kg/tree)
2
l e n t e l ë. Slyvø vaismedþiø ‘Èaèanska Najbolia’ prekinio derliaus
priklausomumas nuo intarpo (kg/medis)
Interstem
Intarpas
Wangenheim Prune
GF 655/2
Early Prune
Sanctus Hubertus
Isthara
2001
2002
2003
2004
Total yield of 20012005 / Suminis
2005
2001–2005 m. derlius
0.48 ns*
0.50 ns
0.55 ns
0.51 ns
0.56 ns
0.99 ns
1.59 ns
1.26 ns
1.44 ns
1.84 ns
4.60 ns
4.80 ns
5.36 ns
4.33 ns
5.08 ns
14.0 ns
16.7 ns
15.7 ns
14.8 ns
12.8 ns
3.32 b**
2.49 a
2.26 a
2.68 ab
2.46 a
23.39 ns
26.08 ns
25.13 ns
23.76 ns
22.74 ns
* no statistical differences / ið esmës nesiskiria
**means followed by the same letters do not differ statistically at probability p = 0.05 / ta
paèia raide paþymëtos reikðmës ið esmës nesiskiria, kai tikimybës lygis p = 0,05
In the first five years of fruiting marketable yield from the plum trees ‘Èaèanska
Najbolia’ growing on Wangenheim Prune rootstock and five interstems did not differ
essentially. In 2005 the differentiation in was noticeable, however many flowers
were damaged as a result of spring frost –5°C (April 22, 2005). The results of 100
fruits mass are presented in Table 3.
T a b l e 3. Mass of 100 fruits of plum ‘Èaèanska Najbolia’ depending
on applied interstem, kg
3
l e n t e l ë. Slyvø vaismedþiø ‘Èaèanska Najbolia’ 100 vaisiø masës
priklausomumas nuo intarpo, kg
Interstem
Intarpas
Wangenheim Prune
GF 655/2
Early Prune
Sanctus Hubertus
Isthara
2001
3.98 ns *
3.98 ns
4.06 ns
3.99 ns
4.18 ns
2002
3.68 ns
3.81 ns
3.89 ns
3.93 ns
4.05 ns
2003
4.53 a**
4.21 ab
3.99 a
3.83 a
4.53 b
2004
4.48 ns
4.40 ns
4.46 ns
4.32 ns
4.42 ns
2005
6.55 ns
5.93 ns
6.00 ns
5.94 ns
6.32 ns
* no statistical differences / ið esmës nesiskiria
**means followed by the same letters do not differ statistically at probability p = 0.05 / ta
paèia raide paþymëtos reikðmës ið esmës nesiskiria, kai tikimybës lygis p = 0,05
The inner quality of plum fruit was estimated by comparison of total soluble
solids content and titratable acidity in the investigated fruit. The results are presented
in Table 4.
237
T a b l e 4. Total soluble solids content – TSS (oBrix) and titratable
acidity – TA (g/100g) of plum ‘Èaèanska Najbolia’
depending on applied interstem
4
l e n t e l ë. Slyvø vaismedþiø ‘Èaèanska Najbolia’ tirpiø sausøjø medþiagø –
TSM (°Brix) ir titruojamojo rûgðtingumo – TR (g/100g)
priklausomumas nuo intarpo
2001
Interstem
TSS
TSM
Intarpas
Wangenheim
Prune
GF 655/2
Early Prune
Sanctus
Hubertus
Isthara
2002
TA
TR
TSS
TSM
2003
TA
TR
TSS
TSM
2004
TA
TR
TSS
TSM
TA
TR
2005
TSS
TSM
TA
TR
14.5 ns * 0.95 ns 13.8 ns 0.84 ns 13.5 ns 0.83 ns 11.7 ns 0.80 ns 12.45a** 1.14a
14.3 ns 0.95 ns 13.4 ns 0.84 ns 13.9 ns 0.86 ns 11.4 ns 0.77 ns 12.18a
13.9 ns 0.93 ns 13.4 ns 0.87 ns 13.6 ns 0.83 ns 12.2 ns 0.84 ns 12.31a
14.9 ns 0.90 ns 13.6 ns 0.85 ns 13.9 ns 0.79 ns 11.6 ns 0.79 ns 12.28a
1.14a
1.14a
1.13a
14.3 ns 0.96 ns 13.2 ns 0.87 ns 13.7 ns 0.85 ns 11.3 ns 0.82 ns 13.40b
1.23b
* no statistical differences / ið esmës nesiskiria
**means followed by the same letters do not differ statistically at probability p = 0.05 / ta
paèia raide paþymëtos reikðmës ið esmës nesiskiria, kai tikimybës lygis p = 0,05
In the first four years of fruiting neither total soluble solids content nor titratable
acidity of fruit differ statistically. Only in 2005 the fruit of ‘Èaèanska Najbolia’ from
the trees growing on interstem Isthara showed both higher TSS and TA.
The greatest differences were noticeable from the growth vigour of plum trees
(Table 5).
T a b l e 5. Trunk cross-section area (TCSA) of plum tree ‘Èaèanska
Najbolia’ and increment of TCSA depending on applied
interstem, cm2
5
l e n t e l ë.
Interstem
Intarpas
Slyvø vaismedþiø ‘Èaèanska Najbolia’ kamieno skerspjûvio ploto
(KSP) ir jo padidëjimo priklausomumas nuo intarpo, cm 2
1999
2000
2001
Wangenheim Prune 2.36ab* 10.50a 17.63a
2002
2003
22.33a
28.93ab
2004
2005
Increment of TCSA
KSP padidëjimas
36.18a 51.74ab
49.38ab
GF 655/2
3.89b 16.32b 21.91ab 32.13b
37.98bc 43.61ab 62.39bc
58.50bc
Early Prune
3.63ab 12.02a 24.95b
42.48c
76.39c
72.76c
Sanctus Hubertus
3.54ab 11.00a 20.49ab 26.11ab 31.26ab 40.34ab 54.75ab
51.21ab
Isthara
2.01a 10.35a 15.88a
39.38a
32.58b
20.73a
24.20a
52.71b
32.26a
41.39a
*means followed by the same letters do not differ statistically at probability p = 0.05 / ta
paèia raide paþymëtos reikðmës ið esmës nesiskiria, kai tikimybës lygis p = 0,05
In all years of experiment the applied interstocks affected significantly the trunk
cross-section area of plum trees ‘Èaèanska Najbolia’. The increasing of that area
after seven years of studies was differentiated. The greatest increase of TCSA was
238
noted for the trees on interstock Early Prune and the least one on interstock Isthara.
Trees on interstem GF 655/2 demonstrated the greatest growth vigour. Only
the trees with interstems Isthara showed weaker growth in comparison with the
trees on interstock Wangenheim Prune. The productivity index displayed the significant
differences between the interstems, the greatest value of index was obtained for
‘Isthara’, and the lowest for interstocks Early Prune (Table 6).
T a b l e 6. Productivity coefficient of plum trees ‘Èaèanska Najbolia’
depending on applied interstem, kg/cm2
6
l e n t e l ë.
Interstem / Intarpas
Slyvø vaismedþiø ‘Èaèanska Najbolia’ produktyvumo koeficiento
priklausomumas nuo intarpo, kg/cm 2
Index of productivity (kg/cm2 of TCSA) / Produktyvumas, kg/cm2 KSP
Wangenheim Prune
GF 655/2
Early Prune
Sanctus Hubertus
Isthara
0.45ab*
0.42ab
0.34a
0.45ab
0.58b
*means followed by the same letters do not differ statistically at probability p = 0.05 / ta
paèia raide paþymëtos reikðmës ið esmës nesiskiria, kai tikimybës lygis p = 0,05
Discussion. Interstocks can be particularly valuable when the scion and
rootstocks are incompatible, they could increase the disease resistance or cold
hardiness of the scion. Mostly the interstocks are used for reducing the vigour of
scion. At the presented experiment five interstocks were applied for reducing tree
growth of cv ‘Èaèanska Najbolia’. This cultivar is one of valuable plum cultivars
because of its biological features – toleration to PPV, high productivity and big fruit
– 60 g. The obtained results are not unequivocal, although there are many reports of
positive effect of applied interstems on yield, health status and frost resistance of
cultivars. (Mielke, Turner, 2002; Grzyb, 2005; Filho et al., 2000; Czynczyk, 2002;
Wertheim, Callesen, 2000; Rozpara, Grzyb, 2004). It is also important to choose the
interstem properly (Rozpara et al., 2004). Propriety of appliance of the interstems
for ‘Èaèanska Najbolia’ cultivar is confirmed by other results concerning the trees
of that cultivar growing on the investigated rootstocks. Comparing the obtained
results with other studies of six-year old trees (Grzyb et al., 1998; Faber et al., 2002)
and seven-year old trees (Rozpara, Grzyb, 1998) using interstocks, we found at
least twofold decreasing of tree trunk cross section area. For plum ‘Ruth Gerstetter’
appliance of the several interstocks (Early Prune, Italian Prune, Opal, Pixy) did not
affect the yield, but the trees with interstems showed higher frost resistance, moreover
Pixy interstem reduced tree productivity and fruit size (Grzyb, Rozpara, 1993). There
is report (Webster, 1995) that Pixy reduced growth vigour of European plum trees
by up to 50% but had only a very small effect on scion vigour when used as an
interstock. These observations indicate that the dwarfing effect shown by plum
rootstock is largely attributable to root rather than shank effect.
In the presented studies the trees started bearing in the fourth year after planting.
239
The greatest yield was obtained in year 2004 (the fourth year of cropping). However,
in the next year strong reduction of yield was noted, because of flower bud damage
by spring frost (on 22 April 2005 air temperature was -5oC). Susceptibility of ‘Èaèanska
Najbolia’ flower buds to the spring frost is confirmed in other report (Sosna, 2000.)
In the presented studies a little higher yield was obtained on the trees with interstocks
compared to the other studies concerning the trees on rootstocks (Grzyb et al.,
1998; Sosna, 2000). Only in year 2005 the significant differences in yield depending
on applied interstem were proved.
There are reports that rootstocks affect (Lipecki et al., 2001) or do not affect
(Szymczak et al., 1998) organic contents in fruit. In carried out experiment the
significant differences in total soluble solids and titratable acidity level were found
only in year 2005. Obtained results concerning soluble solids content in fruit juice of
‘Èaèanska Najbolia’ are similar to those revealed by Lipecki et al. (2001), while
titratable acidity level was higher.
Conclusions. 1. The trees of cv. ‘Èaèanska Najbolia’ on Isthara interstock
revealed the least TCSA and the greatest index of productivity, however, on
Wangenheim Prune interstock they did on the contrary.
2. Applied interstocks did not affect fruit mass and inner quality of ‘Èaèanska
Najbolia’ fruits.
Gauta
2006 04 19
Parengta spausdinti
2006 07 27
References
1. C z y n c z y k A. 2002. The effect of various lengths of P2 interstem on the
growth, yielding, and health of two apple cultivars ‘Gloster’ and ‘Melrose’ // Folia
Horticulturae 14/2: 201–209.
2. D u r i æ G., M i æ i æ N., L u è i æ P. 1997. Growth and bearing potential of
plum cultivars ‘Stanley’ and ‘Po¿egaæa’ on the two stock/interstock combinations and on
Myrobalan // Acta horticulture 478: 225–228.
3. G r z y b Z. S., Z a g a j a S. W., Z d y b J. 1985. Growth and yield of
sweet cherry trees with interstem // Acta horticulture 169:311–318.
4. G r z y b Z. S., R o z p a r a E. 1993. The influence of different interstems on
the growth and yield of ‘Ruth Gerstette’r cv. Trees // Acta horticulturae. Vol.359: 256–259.
5. G r z y b Z. S., R o z p a r a E. 1994. The influence of different interstems on
the growth and yield of ‘Ruth Gerstetter’ plum cv trees // Acta horticulture 359:256–259.
6. G r z y b Z. S., S i t a r e k M., K o z i ñ s k i B. 1998. Effect of different
rootstocks on growth, yield and fruit quality of four plum cultivars (in central Poland) //
Acta horticulturae 478: 239–241.
7. G r z y b Z. S. 2005. Unikatowy sad czereúniowy na wstawkach // Sad
Nowoczesny, 4:26–27.
8. F a b e r T., L e c h W., M a ù o d o b r y M., D z i e d z i c E. 2002.
Assessment of growth and cropping of plum trees grafted on Wangenheim Prune rootstock
and originated from in vitro // Journal of Fruit and Ornamental Plant Research vol. X: 124–129.
240
9. F i l h o J. A., K l u g e R. A., F i l h o V., N e t o J. T. 2000. Behavior of
two peach cultivars with ‘Januaria’ as a Japanese plum interstock // Pesquisa Agropecuaria
Brasileira, vol 35 no.4.
10. L i p e c k i J., J a n i s z A., S z e m b e r E., S i e n k i e w i c z P.
2001. Chemical composition of several plum and prune cultivars // Zeszyty Naukowe IS i
K, t.9: 243–250.
11. M i e l k e E. A., T u r n e r J. 2002. Evaluation of pear interstems. Acta
Horticulturae. 596.:401–404.
12. M i l o s e v i c T. 2006. Effect of interstock on seasonal changes in microelemnt
concentrations in apricot leaf // Acta horticulture 701:719–722.
13. P o n i e d z i a ù e k W. 1995. Dwarfing fruit trees by microinterstock // Materials
of Conference 70 anniversary of Belarus Institute. p: 56.
14. R o d r i g e z R. O., C a s t r o H. R. 2002. The behavior of ‘Old Home’ x
Farmingdale selections interstocks in pear/quince combinations in Rio Negro Valley,
Argentina. // Acta Horticulturae. 596; 373–378.
15. R o z p a r a E., G r z y b Z. S., O l s z e w s k i T. 1990. The mineral
nutrient content in the leaves of two sweet cherry cvs with interstem // Acta horticulture
274: 405-412.
16. R o z p a r a E., G r z y b Z. S. 1998. Growth and yielding of some plum
cultivars grafted on Wangenheim Prune seedlings // Acta horticulturae. Vol. 478: 9194.
17. R o z p a r a E., G r z y b Z. S., O m i e c i ñ s k a B. 2004. The effect of
North Star interstem on the growth, yielding and fruit quality of five sweet cherry cvs. 8th
International Symposium on integrating canopy, rootstock and environmental physiology
in orchard systems, Hungary // Book of Abstracts p: 121.
18. R o z p a r a E., G r z y b Z. S. 2004. Frutana® - A new interstock for sweet
cherry trees // Acta horticulturae. Vol. 658: 247–250.
19. S o s n a I. 2000. Ocena wartoúci produkcyjnej kilkunastu odmian úliw w
poùudniowo-zachodniej Polsce // Materials of International Conference, Limanowa, p: 99–109.
20. S o s n a I. 2002. Growth and cropping of four plum cultivars on different
rootstocks in South Western Poland // Journal of Fruit and Ornamental Plant Research
vol. X:96—104.
21. S z y m c z a k J. A., P ù o c h a r s k i W., G r z y b Z. S. 1998. Wpùyw
podkùadki na jakoúã úliwek // XXXVII Ogólnopolska Konferencja Sadownicza, ISiK :565–570.
22. W e b s t e r A. D. 1995. Rootstock and interstock effects on deciduous fruit
tree vigour, precocity, and yield productivity // New Zealand Journal of Crop and
Horticultural Science, 23: 373–382.
23. W e r t h e i m S. J., C a l l e s e n O. 2000. Results of multi-site interstem
trials with apple trees // Gartenbauwissenschaft 65(6); 251–259.
241
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
235–242.
INTARPØ ÁTAKA SLYVØ VEISLËS ‘ÈAÈANSKA NAJBOLIA‘ VAISMEDÞIØ
AUGIMUI, DERLIUI IR VAISIØ KOKYBEI
E. Dziedzic, M. Maùodobry, W. Lech
Santrauka
Bandymas árengtas 1998 metø pavasará bandymø stotyje netoli Krokuvos. Vaismedþiai
iðauginti, á Wangenheim Prune poskiepá áskiepijus 30 cm ilgio Isthara, Sanctus Hubertus,
Wangenheim Prune, Early Prune, GF 655/2 intarpus ir ‘Èaèanska Najbolia’ veislæ. Vaismedþiai
buvo pasodinti 4 x 2 m atstumais. Tyrimø tikslas buvo nustatyti intarpø átakà vaismedþiø
kamieno skerspjûvio plotui, prekiniam derliui, produktyvumui, vaisiø masei ir vaisiø sulèiø
kokybei. 2001–2005 m. atlikti stebëjimai ir matavimai parodë, kad intarpai turëjo átakos
slyvø vaismedþiø dydþiui.
Reikðminiai þodþiai: ‘Èaèanska Najbolia’, augimo sustabdymas, intarpai, slyvos.
242
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 243–249.
EFFECT OF ROOTSTOCK ON GROWTH AND YIELD OF
PLUM TREE CVS. ‘STANLEY’ AND ‘KAUNO VENGRIN˒
Juozas LANAUSKAS
Lithuanian Institute of Horticulture, Kaunas str. 30, LT–54333 Babtai,
Kaunas distr., Lithuania. E-mail: [email protected]
The experiment was carried out in 1999–2005 at the Lithuanian Institute of Horticulture.
One-year-old plum trees of cvs. ‘Stanley’ and ‘Kauno vengrinë’ were planted to the orchard
in the spring of 1999. Plum trees were grafted on four rootstocks: Prunus cerasifera
seedlings (control rootstock), St. Julien A (P.insititia), St. Julien GF 655/2 (P.insititia) and
Marianna GF 8/1 (P.cerasifera x P.munsoniana). The soil at the experiment place was
Epicalcari–Endohypogleic cambisol, containing 75 mg kg-1 of P2O5, 130 mg kg-1 of K2O,
1.5% of humus, pHKCl – 7.2. Nitrogen fertilizers were used every spring depending on the
tree age at the rate 50–200 g of ammonium nitrate per tree.
Plum tree rootstocks St. Julien A and St. Julien GF 655/2 reduced plum tree trunk
diameter respectively by 6% and 10% in comparison with the P.cerasifera seedlings. Fruit
trees on rootstock GF8/1 were of the same growth vigor as control trees. The highest yield
and yield efficiency was of plum trees grafted on P.cerasifera seedlings. Tested rootstocks
did not influence average fruit weight. The most suckering rootstock was St. Julien
GF 655/2.
Key words: plum tree rootstocks, suckering, trunk diameter, yield efficiency, yield.
Introduction. In Lithuania recently the main rootstocks for plum trees are
seedlings of Prunus cerasifera Ehrh. The most of grown plum cultivars show good
compatibility with this rootstock and start fruiting in the 2–6th year in the orchard
(Lukoðevièius, 1996). Induced vigorous growth and low productivity of scion cultivars
often are indicated as the main limitations of P.cerasifera seedlings (Grzyb et al.,
1998a; Rozpara, Grzyb, 1998). In the orchard trees on P.cerasifera seedlings may
be of uneven growth, if planted to shallow they often sucker.
Seedlings of P.cerasifera do not respond the demands of rootstocks for intensive
plum orchards. Modern rootstocks should decrease fruit tree size, induce early bearing
and ensure big yields of high quality fruits. If plums are grown for processing rootstock
may show higher vigour of growth, but its yield should be efficient.
Results of investigations revealed advantages of some clonal plum rootstocks.
In the Ukraine yield of plums grafted on rootstocks Brompton, GF 667 and
GF 665/2 was about twice higher than on P.cerasifera seedlings (Êîâàëåâà, Ñåíèí,
243
1995). Investigations carried out in Belarus proved higher yield efficiency of clonal
rootstocks as well (Ñàìóñü et al., 1995). Polish scientists established that plums
grafted on ‘Wangenheim Prune’ seedlings or clonal rootstocks St. Julien A, Eruni,
GF 655/2 and Pixy were less vigorous and had higher yield efficiency (Grzyb et al.,
1998a). In Poland seedlings of ‘Wangenheim Prune’ are widely established for plum
tree production. Plum trees on this rootstock usually are of lower growth vigor and
higher yield efficiency in comparison with the ones on P.cerasifera (Rozpara, Grzyb,
1994; 1998). As perspective clonal rootstocks are mentioned St. Julien GF 665/2,
Marianna GF 8/1, Ishtara, etc.
Results on rootstock effects often are diverse and vary on soil and climate
conditions or scion features. In Lithuania clonal plum rootstocks were not investigated.
In earlier experiments there were compared seedlings of P.cerasifera and P.tomentosa.
It was established that P.tomentosa seedlings decreased both growth and yield of
grafted cultivars; there was frequent incompatibility between scion and rootstock
(Kviklys, 1999). P.tomentosa as rootstock for plum trees is undesirable (Kviklys,
1999; Oosten, 1979).
The objective of present research was to evaluate growth and yield of plum tree
cvs. ‘Stanley’ and ‘Kauno vengrinë’ grafted on clonal rootstocks St. Julien A,
St. Julien GF 655/2 and Marianna GF 8/1.
Materials and methods. The experiment was carried out in 1999–2005 at the
Lithuanian Institute of Horticulture. One-year-old plum trees of cvs. ‘Stanley’ and
‘Kauno vengrinë’ were planted in the orchard in the spring of 1999. Plum trees were
grafted on four rootstocks: P.cerasifera seedlings (control rootstock), St. Julien A
(P.insititia), St. Julien GF 655/2 (P.insititia) and Marianna GF 8/1 (P.cerasifera x
P.munsoniana). Each graft combination included sixteen trees portioned into four
plots each of four trees in an overall layout of four randomized blocks. Trees were
spaced at 5x3 m and trained as a spindle bushes. Orchard floor management combined
frequently mown grass in the alleyways with 1.5 m wide herbicide strips along tree
rows. Trees weren’t irrigated. The soil at the experiment place was Epicalcari–
Endohypogleic cambisol, containing 75 mg kg-1 of P2O5, 130 mg kg-1 of K2O, 1.5%
of humus, pHKCl – 7.2. Nitrogen fertilizers were used every spring depending on the
tree age at the rate 50–200 g of ammonium nitrate per tree.
Trunk diameter measurements were done in autumn at 25 cm above the graft
union. Fruit tree flowering abundance was expressed in scores, where 0 – tree do
not flower at all, 5 – tree flower very abundantly. Yield was recorded for the whole
experimental plot consisting of four trees. Yield efficiency was calculated as a sum
of yield efficiencies of two years (2004 and 2005). It is expressed as fruit weight
ratio with trunk cross–section area (TCSA). Average fruit weight was determined
on a representative sample of 100 plums per each experimental plot. Rootstock
suckering was expressed in number of suckers per tree counting them in each plot.
In a young tree age (2001–2003) out of unfavorable meteorological conditions
(spring frosts in 2001 and 2003, draught in 2002) yield was severely decreased.
Experimental data were subjected to analysis of variance. For mean separation
a Duncan’s test at p = 0.05 was used. Data were analysed by ANOVA statistical
program.
244
Results. During the first year of growth ‘Stanley’ trees produced 2.72–3.80 m
of shoots, ‘Kauno vengrinë’ – 3.30–4.32 m (Table 1). Rootstock induced statistically
significant differences were not established, but the tendency of more vigorous tree
growth on rootstocks GF 655/2 and GF 8/1 was observed.
After two years of growth ‘Stanley’ trees grafted on rootstock St. Julien A
were statistically lower in comparison with the rest ones (Table 1). The lowest plum
trees of cv. ‘Kauno vengrinë’ were on rootstock St. Julien A, the tallest – on
GF 8/1. Height differences are statistically reliable. Average data of both cultivars
show that rootstock St. Julien A reduced plum tree height.
T a b l e 1. Rootstock effect on plum tree shoot length and tree
height. Babtai, 1999–2000
1
l e n t e l ë.
Poskiepiø átaka slyvø metûgliø ilgiui ir vaismedþiø aukðèiui.
Babtai, 1999–2000 m.
Total shoot length in 1999
Rootstocks
Poskiepiai
P. cerasifera
St. Julien A
GF 655/2
GF 8/1
Bendras metûgliø ilgis 1999 m., m
‘Stanley’
'Kauno
vengrinë’
Average
2.72 a*
2.75 a
3.60 a
3.80 a
4.22 a
3.30 a
4.26 a
4.32 a
3.47 a
3.02 a
3.93 a
4.06 a
Vidurkis
Tree height in 2000
Vaismedþiø aukðtis 2000 m., m
‘Stanley’
‘Kauno
vengrinë’
Average
3.00 b
2.38 a
2.78 b
2.76 b
2.50 ab
2.25 a
2.56 ab
2.69 b
2.75 b
2.32 a
2.67 b
2.72 b
Vidurkis
* In this and further tables means within the columns followed with the same letter do not
differ statistically at the probability level p=0.05. / Ðioje ir kitose lentelëse tarp skiltyse ta paèia
raide paþymëtø skaièiø esminiø skirtumø nëra (tikimybës lygis p=0,05).
At the end of the experiment tree growth did not differ much. The thinnest
plum tree trunks (8.8 cm) were on rootstock GF 655/2, the thickest ones – on
P. cerasifera seedlings and GF 8/1 (9.8 – 9.9cm) (table 2). Trees on St. Julien A had
trunks of intermediate diameter – 9.2 cm.
The lowest amount of suckers produced rootstocks GF 8/1 and St. Julien A –
on the average 0.4–0.5 pcs. tree-1. The most suckering was rootstock GF 655/2. It
raised 2.4 suckers per tree. Trees on P. cerasifera seedlings produced 1.2 suckers
per tree, mostly from rootstock stem part.
Tree yield in the young age (2001–2003) was decreased because of unfavorable
meteorological conditions. It was similar on all tested rootstocks and reached only
1.30–1.95 t ha-1 (Table 3). Flowering abundance reflects potential yield. Plum trees
flowered medium abundantly in 2001–2003. Average score of flowering did not
depend on rootstock and was in the range 2.25–2.70.
245
T a b l e 2. Rootstock effect on plum tree trunk diameter and
suckering. Babtai, 1999–2005
2
l e n t e l ë.
Rootstocks
Poskiepiø átaka slyvø kamienø skersmeniui ir poskiepiø atþalø
skaièiui. Babtai, 1999–2005 m.
Trunk diameter in 2005
Kamienø skersmuo 2005 m., cm
Poskiepiai
P. cerasifera
St. Julien A
GF 655/2
GF 8/1
‘Stanley’
'Kauno
vengrinë’
Average
9.7 b
9.0 a
8.6 a
9.6 b
9.8 b
9.3 a
9.1 a
10.2 b
9.8 c
9.2 b
8.8 a
9.9 c
Vidurkis
Average number of suckers in 1999 2005,
pcs. tree-1 / Vidutinis poskiepiø atþalø skaièius
1999–2005 m., vnt. vaism.-1
‘Stanley’
‘Kauno
vengrinë’
Average
0.6 ab
0.1 a
2.0 b
0.3 a
1.7 ab
0.9 a
2.8 b
0.4 a
1.2 b
0.5 a
2.4 c
0.4 a
Vidurkis
T a b l e 3. Rootstock effect on plum tree flowering abundance and
yield. Babtai, 2001–2003
3
l e n t e l ë. Poskiepiø átaka slyvø þydëjimo gausumui ir derliui. Babtai,
2001–2003 m.
Flowering abundance (in 0–5 score)
Rootstocks
Poskiepiai
P. cerasifera
St. Julien A
GF 655/2
GF 8/1
Þydëjimo gausumas (0–5 balø skalë)
‘Stanley’
'Kauno
vengrinë’
Average
2.6 a
2.3 a
2.4 a
2.5 a
2.8 a
2.2 a
2.9 a
2.6 a
2.70 a
2.25 a
2.65 a
2.55 a
Vidurkis
Cumulative yield, t ha-1
Suminis derlius, t ha-1
‘Stanley’
‘Kauno
vengrinë’
Average
1.5 a
1.2 a
1.2 a
2.2 a
1.8 a
1.4 a
1.7 a
1.7 a
1.65 a
1.30 a
1.45 a
1.95 a
Vidurkis
In sixth–seventh year of growth yield was higher. Plum trees of cv. ‘Stanley’
yielded similar on all tested rootstocks – 4.8–7.4 t ha-1 (Table 4). The most prolific
plum trees of cv. ‘Kauno vengrinë’ were on P.cerasifera seedlings and rootstock
GF8/1 – respectively 21.5 and 19.7 t ha-1. The average data of both cultivars confirm
that plum trees on P.cerasifera were the most prolific. Plum tree yield on rootstock
GF 8/1 was similar to the one on P.cerasifera seedlings.
T a b l e 4. Rootstock effect on plum tree yield and yield efficiency.
Babtai, 2004–2005
4
l e n t e l ë. Poskiepiø átaka slyvø derliui ir produktyvumui. Babtai, 2004–2005 m.
Cumulative yield, t ha-1
Yield efficiency, kg cm-2 of TCSA
Sumunis derlius, t ha-1
Produktyvumas, kg cm-2 KSP
Rootstocks
Poskiepiai
P. cerasifera
St. Julien A
GF 655/2
GF 8/1
‘Stanley’
'Kauno
vengrinë’
Average
7.4 a
4.8 a
4.8 a
5.2 a
21.5 b
13.6 a
15.6 a
19.7 ab
14.4 b
9.2 a
10.2 a
12.4 ab
Vidurkis
246
‘Stanley’
‘Kauno
vengrinë’
Average
0.16 a
0.12 a
0.14 a
0.12 a
0.49 b
0.34 a
0.42 b
0.42 b
0.32 b
0.23 a
0.28 ab
0.27 ab
Vidurkis
Plum trees of cv. ‘Stanley’ were of similar yield efficiency on all tested rootstocks
– 0.12–0.14 kg cm-2 of TCSA (Table 4). The highest yield efficiency of plum tree cv.
‘Kauno vengrinë’ was on seedlings of P.cerasifera – 0.49 kg cm-2, the lowest one –
on St. Julien A – 0.34 kg cm-2.
Average fruit weight of both cultivars was not affected by tested rootstocks. It
reached 30–32 g for cv. ‘Stanley’ and 17–18 g – for cv. ‘Kauno vengrinë’ (data are
not presented in Table).
Discussion. Rootstock effect on fruit tree adaptability, precocity, growth control,
yield efficiency and fruit quality is well known (Webster, 2001; Botu et al., 2002;
Hrotkó et al., 2002; Botu et al., 2004). In our experiment tested rootstocks had not
big influence on plum tree growth. From the first year plum trees on rootstock
St. Julien A grew somewhat less vigorous and at the end of the experiment their
trunk diameter was by 6% less in comparison with the one on P.cerasifera seedlings.
The young plum trees on rootstock GF 655/2 grew more vigorously but in the
bearing age growth slightly decreased and finally their trunk diameter was by 10%
thinner in comparison with the one on P.cerasifera. Fruit trees on rootstock GF 8/1
were of the same growth vigor as control ones. Our observations in most cases are
in consistence with the results of the other experiments (Hrotkó et al., 1998; Sosna,
2002).
Yield and yield efficiency in our experiment was the highest of plum trees on
P.cerasifera seedlings. Though in the most other experiments clonal rootstocks
improve plum tree productivity (Grzyb et al., 1998b; Hrotkó et al., 2002), there are
cases when trees on P.cerasifera seedlings were the most prolific (Grzyb et al.,
1998c). Growth and yield of different scion–rootstock combinations depends on
soil and climate conditions and the results may vary (Sitarek et al., 2004).
Information about rootstock effect on fruit weight is diverse. Usually plum tree
rootstocks have not significant effect on this fruit quality trait (Hrotkó et al., 2002;
Sosna 2002; Grzyb et al., 1998b). In some cases it is reported about negative effect
of Pixy rootstock on fruit weight (Ystaas et al., 1994; Grzyb et al., 1998c). In our
experiment tested rootstocks did not influence average fruit weight.
From practical side valuable are non–suckering rootstocks. It alleviates orchard
floor management. Rootstocks St. Julien A and GF 8/1 practically did not sucker.
When trees on P. cerasifera seedlings were planted too shallowly they produced few
suckers, mostly from rootstock stem part. The most suckering rootstock was
GF655/2. Similar information on this rootstock is presented from the other researches
(Kosina et al., 2000; Sosna, 2002).
According to data of our experiment none of tested rootstocks was better than
standard P.cerasifera.
Polish scientists in recent years revealed advantages of Wangenheim Prune
seedling rootstocks. Scion cultivars on this rootstock often are of superior
characteristics in comparison with P.cerasifera seedlings or clonal rootstocks (Grzyb
et al., 1998b; Rozpara, Grzyb, 1998; Sitarek et al., 2004). In the nearest future
Wangenheim Prune seedlings should be introduced into rootstock tests in Lithuania.
247
Conclusions. Plum tree rootstocks St. Julien A and St. Julien GF 655/2 reduced
plum tree trunk diameter respectively by 6% and 10% in comparison with the
P.cerasifera seedlings.
The highest yield and yield efficiency was of plum trees grafted on P.cerasifera
seedlings.
Tested rootstocks did not influence average fruit weight.
The most suckering rootstock was St. Julien GF 655/2.
Gauta
2006 07 06
Parengta spausdinti
2006 07 31
References
1. B o t u I., A c h i m G . , B o t u M . , G o d e a n u I . , B a c i u A .
The evaluation and classification of growth vigor of the plum cultivars grafted on various
rootstocks // Acta Hort. 2002. Vol. 577. P. 299–306.
2. B o t u I., A c h i m G., B o t u M. Evaluation of the stress capacity of
different soil types on the scion – rootstock biosystem for plum // Acta Hort. 2004. Vol. 658
P. 413–419.
3. G r z y b Z. S., G u z o w s k a – B a t k o B., K o l o d z i e j c z a k P.
Ocena podkladek dla sliw // Sprawodzanie roczne: sadownictwo, rosliny ozdobne,
pszczelnictwo. Skierniewice. 1998a. P. 219–222.
4. G r z y b Z. S., S i t a r e k M., K o l o d z i e j c z a k P. Growth and yield
of three plum cultivars grafted on four rootstocks in piedmont area // Acta Hort. 1998b.
Vol. 478. P. 87–90.
5. G r z y b Z. S., S i t a r e k M., K o z i n s k i B. Effect of different
rootstocks on growth, yield and fruit quality of four plum cultivars (in central of poland) //
Acta Hort. 1998c. Vol. 478. P. 239–242.
6. Hrotkó K., Magyar L., Klenyán T., Simon, G. Effect of rootstocks on growth and
yield efficiency of plum cultivars // Acta Hort. 2002. Vol. 577. P. 105–110.
7. H r o t k ó K., M a g y a r L., S i m o n G., K l e n y á n T. Effect of
rootstocks on growth of plum cultivars in a young orchard // Acta Hort. 1998. Vol. 478.
P. 95–98.
8. K o s i n a J. Evaluation of some new plum rootstocks in the orchard // Acta
Hort. 2000. Vol. 538. P. 757–760.
9. K v i k l y s D. Slyvø veisliø ir poskiepiø tyrimas sode // Sodininkystë ir
darþininkystë. 1999. T. 18(4). P. 38–45.
10. L u k o ð e v i è i u s A., L a p i n s k a s E., M i s e v i è i û t ë A. ir kt.
1996. Lietuvos pomologija. Mokslo ir enciklopedijø leidykla. T. 2. P. 7–58.
11. O o s t e n H. I. Research on culture in fruit nurseries // Annual reports.
Wilhelminadorp. 1979. P. 21.
12. R o z p a r a E., G r z y b Z. S. Growth and cropping of twelve plum
cultivars grafted to two rootstocks // Acta Hort. 1994. Vol. 359. P. 229–236.
13. R o z p a r a E., G r z y b Z. S. Growth and yielding of some plum cultivars
grafted on ‘Wangenheim Prune’ seedlings // Acta Hort. 1998. Vol. 478. P. 87–90.
248
14. S i t a r e k M., G r z y b Z. S., G u z o w s k a – S p a l e n i a k B.,
L i s J. Performance of three rootstocks for plums in two different soils and climatic
conditions // Acta Hort. 2004. Vol. 658. P. 273–277.
15. S o s n a I. Growth and cropping of four plum cultivars on different rootstocks
in south western Poland // Journal of fruit and ornamental plant research. 2002. Vol. 10.
P. 95–103.
16. W e b s t e r A. D. Rootstocks for temperate fruit crops: current uses, future
potential and alternative strategies // Acta Hort. 2001. Vol. 557. P. 25–34.
17. Y s t a a s J., M a g e F., H u s a b o., F r y n e s O. Performance of
Eruni and Pixi as rootstocks for European plum cultivars // Norw. J. Agric. Sci. 1994. Vol. 8.
P. 115–126.
18. Ê î â à ë å â à À. Ô., Ñ å í è í Â. È. Íîâûå ïîäâîè äëÿ ñëèâû
íà þãå Óêðàèíû // Òåç. äîêë. íàó÷. êîíô. «Ñîâðåìåííûå ïðîáëåìû
ñàäîâîäñòâà». Ñàìîõâàëîâè÷è. 1995. Ñ. 138.
19. Ñ à ì ó ñ ü Â. À., × å ë î ì á è ò ü ê î Ì. À., Ô å ä ó ð ê î Ò. À.
Ðîñò è ïëîäîíîøåíèå äåðåâúåâ ñëèâû, âûðàùèâàåìûõ íà êëîíîâûõ
ïîäâîÿõ // Òåç. äîêë. íàó÷. êîíô. «Ñîâðåìåííûå ïðîáëåìû ñàäîâîäñòâà».
Ñàìîõâàëîâè÷è. 1995. Ñ. 138.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
243–249.
POSKIEPIØ ÁTAKA ‘STANLEY’ IR ‘KAUNO VENGRINËS’ VEISLIØ SLYVØ
VAISMEDÞIØ AUGIMUI IR DERËJIMUI
J. Lanauskas
Santrauka
Tyrimai daryti 1999–2005 m. Lietuvos sodininkystës ir darþininkystës institute.
‘Stanley’ ir ‘Kauno vengrinës’ veisliø slyvø vienameèiai sodinukai á sodà pasodinti
1999 m. pavasará. Vaismedþiai buvo skiepyti á keturis poskiepius: Prunus cerasifera
sëjinukus (kontrolinis poskiepis), St. Julien A (P.insititia), St. Julien GF 655/2 (P.insititia)
ir Marianna GF 8/1 (P.cerasifera x P.munsoniana). Dirvoþemis bandymø vietoje buvo
sekliai karbonatingas, giliau – glëjiðkas rudþemis. Agrocheminës dirvoþemio
charakteristikos: P2O5 – 75 mg kg-1, K2O – 130 mg kg-1, humuso – 1,5%, pHKCl – 7,2. Azoto
tràðomis vaismedþiai buvo træðti kiekvienà pavasará – po 50–200 g amonio salietros
vaismedþiui, priklausomai nuo amþiaus.
Poskiepiai St. Julien A ir St. Julien GF 655/2 sumaþino slyvø kamienø skersmená
atitinkamai 6 ir 10%, palyginti su P.cerasifera sëjinukais. Vaismedþiai su GF 8/1 poskiepiu
augo taip pat, kaip skiepyti á P.cerasifera sëjinukus. Derlingiausios ir produktyviausios
buvo slyvos su P.cerasifera sëkliniais poskiepiais. Tirti poskiepiai neturëjo átakos vidutinei
vaisiaus masei. Daugiausia ðaknø atþalø iðaugino GF 655/2 poskiepis.
Reikðminiai þodþiai: derlius, kamieno skersmuo, poskiepio atþalos, produktyvumas,
slyvø poskiepiai.
249
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 250–257.
ESTIMATION OF SEVERAL PLUM CULTIVARS ON FOUR
ROOTSTOCKS
Ireneusz SOSNA
Department of Horticulture, Agricultural University in Wrocùaw, Rozbrat 7,
50-334 Wrocùaw, Poland. E-mail: [email protected]
The experiment was conducted at Fruit Experimental Station near Wrocùaw in 1995–
2004. The testing material included one-year-old maidens of four new plum cultivars on
seedlings ‘Wangenheim Prune’, Pixy, GF 655/2 and St. Julien A. Rootstocks were planted
at a spacing of 4 x 2 m (1250 trees per ha) in the spring of 1995. Up to the tenth year after
planting, growth, yield, fruit quality and survival were affected by cultivar and rootstock.
Cultivars ‘Èaèanska Rana’, ‘Empress’ and ‘Oneida’ were the most productive on rootstock
GF 655/2. Total yields per tree from 1996 to 2004 were the highest with trees ‘Èaèanska
Najbolja’ on St. Julien A. Seedlings Pixy and especially ‘Wangenheim Prune’ reduced
vegetative growth of plum cultivars in comparison to rootstocks GF 655/2 and St. Julien A.
Type of rootstock had no influence on mean fruit weight of cultivars ‘Empress’ and ‘Oneida’.
Bigger fruit were picked from trees ‘Èaèanska Rana’ and ‘Èaèanska Najbolja’ budded on
more vigorous rootstocks GF 655/2 and St. Julien A. Significantly the most root suckers
were observed on rootstock GF 655/2.
Key words: cultivar, fruit quality, growth, plum, rootstocks, root suckers, yield.
Introduction. During the last years, on Polish nursery fields, orchards and
commercial markets a lot of plum varieties appeared which are highly tolerant to
plum pox, very early start to bear, are highly productive and have attractive, large
and tasty fruits. Greater chances for a profitable sale are given by cultivars with very
early ripening fruits, such as ‘Herman’, ‘Èaèanska Rana’ and ‘Sanctus Hubertus’,
and those late ripening, which fruits can be stored even for 2-3 weeks, for example
‘President’, ‘Oneida’ and ‘Elena’ (Sosna, 2004). But modern fruit growing does not
mean only cultivar. Very important are rootstocks suitable for a high-density plum
orchard. Knowledge about usefulness of different types of rootstocks for different
varieties is still very limited. Rootstock can affect not only vegetative growth but
also yield and fruit quality. The most popular vigorous rootstock in plum orchards
(not only in Poland) is seedling Myrobalan (Prunus cerasifera). Unfortunately, it is
not the best one, especially for varieties with a strong vegetative growth (Grzyb et
al., 1998; Kosina et al., 2000). Besides Prunus cerasifera, seedlings ‘Wangenheim
Prune’ also are important in Polish nursery production. In comparison to seedlings
250
Myrobalan, plum trees grafted on semi-dwarf rootstock ‘Wangenheim Prune’ grow
weaker and are more productive (Rozpara and Grzyb, 1998; Blaþek et al., 2004). At
present, vegetative propagated rootstocks, such as Pixy, GF 655/2 and St. Julien A
have very important role in the intensification of plum orchard. Their suitability for
cultivation is evaluated in many countries of the world (Embree et al., 1999; Sitarek
et al., 2001; Rubauskis et al., 2002; Jänes and Pae, 2003). Planting plum trees grafted
on dwarf or semi-dwarf rootstocks enables an increase of tree number in a row and
leads to a higher yield per unit area with a decrease of tree growth vigour (Botu et al.,
1998; Kosina, 2000).
The aim of this study was to estimate production value of several plum cultivars
on different rootstocks in the Lower Silesia climatic conditions.
Materials and methods. In the spring of 1995 the experiment was established
at the Fruit Experimental Station in Samotwór, near Wrocùaw. One-year-old trees of
four plum cultivars – ‘Èaèanska Rana’, ‘Èaèanska Najbolja’, ‘Empress’ and ‘Oneida’
budded on seedlings Wangenheim Prune (generative rootstock) and three vegetative
rootstocks Pixy, GF 655/2 and St. Julien A were planted 4 x 2 m apart
(1250 trees/ha) in a randomized block design with four replications of four trees per
plot. All the trees were trained as spindles. Pruning was carried out immediately after
blossoming. Herbicide fallow was maintained in tree rows and grassy strips between
them. Plant protection was carried out in accordance with the current
recommendations of the Orchard Protection Program. Up to the tenth year after
planting, growth, yield, fruit quality and longevity of trees were estimated. Trunk
girth at 30 cm above the ground was recorded annually from each tree. Root suckers
were counted and then removed during vegetative period. Since the fourth year, the
width and height of each plum tree was recorded. The calculation of crown volume
was based on formula on volume of cone. The size of a fruit was estimated as a
mean weight of 25 fruits per tree.
The results were analysed statistically, using the analysis of variance. Significant
differences at P=0.05 were calculated using t-Student test.
Results and discussion. Up to the tenth year after planting, vegetative growth
was significantly affected both by cultivar and rootstock (Table 1). Trees of ‘Èaèanska
Najbolja’ were the most vigorous, while ‘Empress’ was characterised by the weakest
growth, especially on seedlings ‘Wangenheim Prune’. Thus, this rootstock appeared
to be too dwarf for ‘Empress’. Similar results were obtained by Wociór et al. (2003)
and Blažek et al. (2004). In this experiment, irrespective of the cultivar, trees grafted
on seedlings Pixy and ‘Wangenheim Prune’ were less vigorous in comparison to
rootstocks GF 655/2 and St. Julien A. Similar results connected with influence of
rootstock Pixy on reduction of tree growth have been reported by Botu et al. (1998),
Embree et al. (1999) and Kosina et al. (2000). In Sitarek et al. (2000) studies, trees
grafted on seedlings‘Wangenheim Prune’ grew considerably weaker in comparison
to other generative rootstocks. According to Hrotko et al. (2002), in comparison to
different types of Myrobalan, small tree size was achieved on GF 655/2 and St.
Julien. Plum trees on GF 655/2 had significantly the biggest number of root suckers.
This fact has been confirmed by Kosina et al. (2000) and Sitarek et al. (2001). Trees
on rootstocks ‘Wangenheim Prune’ and St. Julien A produced only few suckers.
251
T a b l e 1. Vegetative growth of evaluated plum cultivars depending
on rootstock
1
l e n t e l ë. Vegetatyvinio slyvø veisliø augimo priklausomumas nuo poskiepio
Cultivar / Rootstock
Veislë / Poskiepis
Trunk cross sectional
area / Kamieno skerspjûvio
2
plotas, cm
autumn of
2004
2004 m.
rudená
increment
2002–2004
padidëjimas
2002–2004 m.
Volume of
crown (m3),
autumn of
2002
Volume of
crown (m3),
autumn of
2004
Vainiko dydis
2002 m. rudená,
m3
Vainiko dydis
2004 m. rudená,
m3
Root suckers
(no tree-1)
Ðaknø atþalos
2000–2004 m.
vnt. medžio-1
‘Èaèanska Rana’
‘Wangenheim Prune’
69.9
GF 655/2
100.7
Pixy
84.8
St. Julien A
93.4
Mean for cultivar
87.2
Veislës vidurkis
11.8
4.0
6.1
9.0
15.8
6.1
8.4
218.3
20.4
2.7
4.1
67.2
16.9
4.3
5.8
2.1
16.2
4.3
6.1
74.2
5.7
6.1
‘Èaèanska Najbolja’
‘Wangenheim Prune’
87.6
12.4
4.2
GF 655/2
111.1
16.1
6.7
7.8
260.0
Pixy
119.4
17.5
3.7
4.6
88.1
St. Julien A
135.7
22.0
6.3
6.9
1.7
Mean for cultivar
113.5
17.0
5.2
6.3
89.0
3.8
1.9
2.2
0.2
Veislës vidurkis
‘Empress’
‘Wangenheim Prune’
27.1
GF 655/2
41.0
4.3
2.8
3.6
21.7
Pixy
St. Julien A
40.2
5.8
2.5
3.4
0.5
Mean for cultivar
36.1
4.6
2.4
3.1
7.5
Veislës vidurkis
‘Oneida’
‘Wangenheim Prune’
65.0
9.4
3.3
4.8
1.7
GF 655/2
Pixy
St. Julien A
79.1
-
10.0
-
4.2
-
5.7
-
85.3
-
Mean for cultivar
72.1
9.7
3.8
5.3
43.5
LSD05 for cultivar
7.4
1.8
0.5
0.6
26.2
LSD05 for rootstock
within cultivar
14.8
3.7
0.9
1.1
52.4
Veislës vidurkis
Veislës R05
Veislës poskiepio R05
252
There were significant yield differences between cultivars during 1996–2004
(Table 2). Irrespective of rootstock, total yields per tree during this period were
T a b l e 2. Yielding of studied plum cultivars on several rootstocks
and crop efficiency index (CEC); trees were planted in the
spring of 1995
2 l e n t e l ë. Tirtø slyvø veisliø su keliais poskiepiais derlius ir
produktyvumas; vaismedþiai pasodinti 1995 m. pavasará
Yield, kg/tree
Cultivar / Rootstock
Veislë / Poskiepis
Total yield, kg
tree-1 1996–2004
Derlius, kg/medis
CEC 1996–2004
(kg cm-2)/
Suminis derlius
1996–2004 m.
kg medis-1
Produktyvumas 1996–
2004 m., kg cm-2
27.9
81.0
1.16
1.5
37.1
84.4
0.84
2.5
17.1
44.6
0.53
18.6
3.7
29.1
74.2
0.79
18.4
2.8
27.8
71.1
0.83
1996–2001
2002
30.2
19.6
3.3
GF 655/2
23.5
22.3
Pixy
11.9
13.1
St. Julien A
22.8
Mean for cultivar
22.0
‘Wangenheim Prune’
44.6
36.4
GF 655/2
47.8
Pixy
30.2
St. Julien A
Mean for cultivar
2003 2004
‘Èaèanska Rana’
‘Wangenheim Prune’
Veislës vidurkis
‘Èaèanska Najbolja’
Veislës vidurkis
9.9
45.7
136.6
1.56
46.4
8.8
61.2
164.2
1.48
32.0
15.3
34.0
111.5
0.93
40.5
45.5
17.6
67.7
171.3
1.26
40.9
40.1
12.9
52.2
145.9
1.31
‘Empress’
‘Wangenheim Prune’
62.0
14.4
GF 655/2
107.4
Pixy
St. Julien A
66.5
-
Mean for cultivar
78.6
Veislës vidurkis
9.6
13.3
99.3
3.66
18.8
21.5
22.9
170.6
4.16
16.1
-
16.0
-
19.
-
117.9
-
2.93
-
16.4
15.7
18.5
129.3
3.58
‘Oneida’
‘Wangenheim Prune’
84.6
31.5
26.7
37.3
180.1
2.77
GF 655/2
Pixy
St. Julien A
101.8
-
37.6
-
26.8
-
38.8
-
205.0
-
2.59
-
Mean for cultivar
93.2
34.6
26.8
38.1
192.6
2.68
LSD05 for cultivar
8.2
3.0
3.4
3.9
11.0
0.14
LSD05 for rootstock
within cultivar
16.4
5.9
6.8
7.9
22.1
0.28
Veislës vidurkis
Veislës R05
Veislës poskiepio R05
253
significantly the highest with ‘Oneida’. The lowest yields were obtained from
‘Èaèanska Rana’. These results are similar to those reported in literature (Blaþek et
al. 2004; Wociór et al. 2003). Up to the tenth year after planting, total yields per tree
of all evaluated plum cultivars were the highest on rootstock GF 655/2. Yields of
trees on Pixy were lower than on other rootstocks, with the exception of ‘Empress’,
for which the lowest crops were obtained on seedlings ‘Wangenheim Prune’ (very
weakly growing trees). The reduction in yield of plum trees on Pixy as compared
with other rootstocks was also reported by Kosina et al. (2000) and Sitarek et al.
(2001). Crop efficiency index (CEC) was significantly the highest of weakly growing
‘Empress’ and clearly the lowest of ‘Èaèanska Rana’. Cumulative yield efficiency
for three studied cultivars was the highest on seedlings ‘Wangenheim Prune’, whereas
for ‘Empress’ on GF 655/2. Trees on Pixy had the lowest CEC. These results are
consistent with observations of Boyhan et al. (1998) who reported that yield efficiency
was significantly lower of plum cultivar ‘Producer’ on Pixy.
In the present study the cultivar had no significant effect on fruit size (Table 3).
The influence of rootstocks on mean fruit weight was different and depended on
cultivar. Pixy showed negative effect on mean fruit weight of ‘Èaèanska Rana’ and
‘Èaèanska Najbolja’. This is in agreement with the results of other scientists who
declare that trees on Pixy produced smaller fruits (Grzyb at al., 1998; Embree at al.,
1999). However, this contradicts to the studies by Sitarek et al. (2001), Hrotko et al.
(2002) and Rubauskis et al. (2002) who noted similar fruit size on different rootstocks.
In Jänes and Pae (2003) investigation, trees on Pixy gave the largest fruits.
Among estimated rootstocks, Pixy appeared to be the most sensitive to frost.
The great number of died trees on rootstock Pixy was caused by frost injures after
severe winter in 1996/97 (Table 3). This agrees with an earlier report that only 47%
of plum trees on Pixy survived (Boyhan et al., 1998). During the same winter, there
were not observed any frost injures on trees grafted on other rootstocks. Until 2004,
only 5 dead trees were recorded on seedlings ‘Wangenheim Prune’, mainly with
‘Empress’.
254
T a b l e 3. Mean fruit weight and longevity of four plum cultivars
depending on rootstock
3
l e n t e l ë.
Keturiø slyvø veisliø vidutinës vaisiø masës ir ilgaamþiðkumo
priklausomumas nuo poskiepio
Mean fruit weight
Cultivar / Rootstock
Veislë / Poskiepis
Vidutinë vaisiaus masë,
2002
2003
2004
Percent of survived trees in
autumn of 2004
g
1997–2004
2004 m. rudená iðlikusiø medþiø
procentas
‘Èaèanska Rana’
‘Wangenheim Prune’
45
56
33
51
93.7
GF 655/2
55
56
35
54
100.0
Pixy
41
54
34
50
75.0
St. Julien A
51
59
34
51
100.0
Mean for cultivar
48
56
34
51
92.2
Veislës vidurkis
‘Èaèanska Najbolja’
‘Wangenheim Prune’
44
48
36
50
100.0
GF 655/2
54
51
40
52
100.0
Pixy
48
44
38
49
50.0
St. Julien A
59
52
42
54
100.0
Mean for cultivar
51
49
39
51
87.5
Veislës vidurkis
‘Empress’
‘Wangenheim Prune’
39
49
34
51
75.0
GF 655/2
47
46
35
53
100.0
Pixy
St. Julien A
37
-
51
-
35
-
53
-
50.0
-
Mean for cultivar
41
49
35
52
75.0
Veislës vidurkis
‘Oneida’
‘Wangenheim Prune’
42
40
40
51
100.0
GF 655/2
Pixy
St. Julien A
46
-
39
-
40
-
51
-
100.0
-
Mean for cultivar
44
40
40
51
100.0
LSD05 for cultivar
3
4
2
n.s.
LSD05 for rootstock
within cultivar
7
8
4
3
Veislës vidurkis
Veislës R05
Veislës poskiepio R05
Conclusions. 1. Data of the study proved that ‘Oneida’ and ‘Èaèanska Najbolja’
appeared to be the most profitable among studied plum cultivars because of high and
early cropping and quality of fruit. Trees of cultivar ‘Empress’ on rootstock Pixy
grew too weakly.
255
2. Taking into account productivity and fruit quality, the best rootstock for
evaluated plum cultivars was GF 655/2. Rootstocks Pixy and ‘Wangenheim Prune’
reduced vegetative growth of plum cultivars in comparison to GF 655/2 and
St. Julien A.
3. Irrespective of cultivar, the most root suckers were found on trees grafted
on rootstock GF 655/2. Very few suckers produced rootstocks ‘Wangenheim Prune’
and St. Julien A.
4. Frost injures which were observed on rootstock Pixy considerably limited its
suitability in Polish climate conditions.
Gauta
2006 04 27
Parengta spausdinti
2006 07 13
References
1. B l a þ e k J., V á v r a R., P i š t ì k o v á I. Orchard performance of new
plum cultivars on two rootstocks in a trial at Holovousy in 1998–2003 // Horticultural
Science. 2004. Vol. 31(2). P. 37-43.
2. B o t u I., A c h i m G., B a d e a J. Behaviour of some plum rootstocks in
Romania’s conditions // Acta Horticulture. 1998. Vol. 478. P. 229-237.
3. B o y h a n G. E., N o r t o n J. D., P i t t s J. A., H i m e l r i c h D.
G. Growth, yield, survival and leaf nutrient concentrations of plums on various rootstocks //
Fruit Varieties Journal. 1998. 52(2). P. 71-79.
4. E m b r e e C. G., T e h r a n i G., M c R a e K. B. Vineland plum
cultivars perform well on dwarf and vigorous rootstocks in early production // Canadian
Journal of Plant Science. 1999. Vol. 79(4). P. 611-615.
5. G r z y b Z. S., S i t a r e k M., K o z i ñ s k i B. Effect of different
rootstocks on growth, yield and fruit quality of four plum cultivars (in central Poland) //
Acta Horticulturae. 1998. Vol. 478. P. 239-242.
6. H r o t k o K., M a g y a r L., K l e n y a n T., S i m o n G.,
G e r c h e v a P. Effect of rootstocks on growth and yield efficiency of plum cultivars /
/ Acta Horticulturae. 2002. Vol. 577. P. 105-110.
7. J ä n e s H., P a e A. First results of a dwarfing plum rootstocks trial //
Agronomy Research. 2003. Vol. 1(1). P. 37-44.
8. K o s i n a J., G e i b e l M., F i s c h e r M., F i s c h e r C. Evaluation
of some new plum rootstocks in the orchard // Acta Horticulturae. 2000. Vol. 538(2). P. 757-760.
9. R o z p a r a E., G r z y b Z. S. Growth and yielding of some plum cultivars
grafted on Wangenheim Prune seedlings // Acta Horticulturae. 1998. Vol. 478. P. 87-90.
10. R u b a u s k i s E., S k r i v e l e M., D i m z a I., B e r l a n d s V.
Effect of fertigation on growth and precocity of plums depending on a rootstock //
Horticulture and Vegetable Growing. 2002. Vol. 21(4). P. 50-57.
11. S i t a r e k M., G r z y b Z. S., L i s J. Wzrost i owocowanie úliw
szczepionych na podkùadkach generatywnych w pierwszych czterech latach po posadzeniu
// Zeszyty Naukowe A. R. Poznañ – Ogrodnictwo. 2000. Vol. 31(2). P. 145-149.
12. S i t a r e k M., G r z y b Z. S., K o ù o d z i e j c z a k P. Effect of
rootstocks on growth and yield of plum trees // Journal of Fruit and Ornamental Plant
Research. 2001. Vol. IX(1-4). P. 19-24.
256
13. S o s n a I. Ocena wartoúci produkcyjnej kilkudziesiêciu odmian úliwy na
podkùadce z aùyczy w rejonie Wrocùawia // Acta Scientiarum Polonorum. Hortorum Cultus.
2004. Vol. 3(1). P. 47-54.
14. W o c i ó r S., P ù a z a E., W ó j c i k I. Badania plonowania kilku odmian
úliw na Wyýynie Sandomierskiej // Folia Horticulturae. 2003. Supplement 1. P. 164-166.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
250–257.
KELIØ VEISLIØ SLYVØ SU KETURIAIS POSKIEPIAIS ÁVERTINIMAS
I. Sosna
Santrauka
Bandymas atliktas Sodininkystës tyrimø stotyje netoli Vroclavo 1995–2004 metais.
Buvo tirti keturiø naujø slyvø veisliø vienameèiai sodinukai su ‘Wangenheimo vengrinës’,
Pixy, GF 655/2 ir St. Julien A poskiepiais. Sodas pasodintas 1995 metø pavasará 4 x 2 m
(1250 medþiø/ha) atstumais. Iki deðimtø metø po pasodinimo augimui, derliui, vaisiø kokybei
ir laikymuisi átakos turëjo ir veislë, ir poskiepis. ‘Èaèanska Rana’, ‘Empress’ ir ‘Oneida’
veislës buvo derlingiausios su GF 655/2 poskiepiu. 1996–2004 metais didþiausià bendrà
medþio derliø davë ‘Èaèanska Najbolja’ veislës vaismedþiai su St. Julien A poskiepiu.
Sëkliniai poskiepiai Pixy ir ypaè ‘Wangenheimo vengrinë’ sumaþino vegetatyviná slyvø
veisliø augimà, palyginti su GF 655/2 ir St. Julien A poskiepiais. Poskiepio rûðis neturëjo
átakos ‘Empress’ ir ‘Oneida’ veisliø vidutinei vaisiø masei. Didesni vaisiai skinti nuo
‘Èaèanska Rana’ ir ‘Èaèanska Najbolja’ veisliø vaismedþiø, áskiepytø á augesnius
GF 655/2 ir St. Julien A poskiepius. Ið esmës daugiausia ðaknø atþalø iðaugino GF 655/2
poskiepis.
Reikðminiai þodþiai: veislë, vaisiø kokybë, augimas, slyvos, poskiepiai, ðaknø atþalos,
derlius.
257
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3).
258–263.
ROOTSTOCK EFFECT ON MATURITY AND QUALITY OF
‘AUKSIS’ APPLES
Nomeda KVIKLIENË, Darius KVIKLYS
Lithuanian Institute of Horticulture, LT–54333 Babtai, Kaunas distr.,
Lithuania. E-mail: [email protected]
The effects of 12 rootstocks – P 22, P 2, M.9, B.9, Pure 1, B.491, B.146, York 9, B.396,
P 60, M.26 and Bulboga on ‘Auksis’ apples were studied at the Lithuanian Institute of
Horticulture in 2004–2005. The influence of rootstocks on yield, distribution of fruit size,
fruit colour and maturity was evaluated. The average yield per tree was the highest from
trees on rootstocks Pure 1, B.146 and Bulboga, while the lowest on rootstocks P 2, B.396
and P 22 that had the lowest vigour. Fruit size generally depended on crop load and tree
vigour. High yielding trees on dwarf rootstock Pure 1 have the smallest fruits. Largest
fruits were on strong growing Bulboga, B.146 and dwarf rootstock M.9. Pure 1 and P 22
determined better fruit colouring. Fruits on Bulboga were firmer, and these on rootstock
P 2 – softer. P 2 determined higher content of soluble solids. The maturity index indicated
that ‘Auksis’ apples were more mature from trees on rootstock Pure 1. Rootstock Bulboga
produced later ripening of apples.
Key words: fruit quality, Malus x domestica Borkh., maturity index, rootstock.
Introduction. Apple tree growth, beginning of bearing, productivity and fruit
quality depend on rootstock (Webster, 1993). Fruits on dwarf rootstocks usually
have better quality parameters than fruits on strong growing trees (Tomala, 1999;
Skrzynski, 1997). Fruit development processes and ripening peculiarities vary
according to the rootstock type (Jager, 1996). In Poland it was proved that rootstocks
of M series influenced bigger fruits and rootstocks of P series – fruit colour
(Kruczynska et al., 1999; Maas, Wertheim, 2004). Super dwarf rootstock P 22
negatively affects fruit weight (Jadczuk, Wlosek-Staugut, 1999; Ystaas, Froines 1993).
Rootstocks of B series mainly are recommended to grow as winterhardy rootstocks
instead of M.9 under more severe climatic conditions (Wertheim, 1998). Some
rootstocks of B series have positive effect on fruit calcium content (Maas, Wertheim,
2004).
Fruit internal characters like flesh firmness, soluble solids and starch content
depend on rootstock and determine storage durability of apple fruits (Autio et al.,
1996; Barden, Marini, 1992, 2001). Rootstock effect on fruit quality varies under
258
different climatic conditions and is not stable (Al-Hinai, Roper, 2004).
The aim of the trial was to define rootstock effect on apple fruit quality and
maturity of cv. ‘Auksis’.
Material and methods. The trial was performed at the Lithuanian Institute of
Horticulture in 2004–2005. ‘Auksis’ apple trees were grafted on rootstocks M.26,
M.9, York 9, B.9, B.396 (original name 62-396), B.146 (original name 57-146),
B.491 (original name 57-491), P 60, P 22, P 2, Bulboga (Moldavian selection) and
Pure 1 (Latvian selection). The orchard was planted in the spring of 2001. Planting
distances were 4 x 1.5 m. Trees were trained as slender spindles. The trial consisted
of four replications with 3 trees in each. Replications were randomised.
From each replication 100 fruits were weighed and sized as follows:
60-65 mm, 66-75 mm, 76-85 mm and 86-95 mm.
Ten fruits from each replication were taken for laboratory measurements. Fruit
firmness was measured with Effegi penetrometer (with 11 mm diameter probe).
Starch conversion was estimated after treatment with 0.1n iodine and potassium
iodine solution (scale 1-10). Concentration of soluble solids was determined with a
refractometer. Measurements were taken at harvest time. Maturity index was
calculated as F/RS, where F – firmness, R – concentration of soluble solids,
S – starch conversion (Streif, 1996). Since interaction between year and rootstock
is absent, data of internal fruit quality is presented as two-years average.
Variance analysis was done with a LSD test using the ANOVA statistical program.
Results. Significantly highest average yield per tree was obtained on rootstock
Pure1 – 18.10 kg (Table 1). High yield was obtained on York 9 too. Among dwarf
rootstocks lower yields were on P 22, P 2 and B.396. In more vigorous rootstock
group Bulboga and B.146 gave higher yields. There were no significant differences
among rootstocks P 60, M.9, M.26 and B.491.
Rootstock Pure 1 produced significantly the smallest fruits of average weight
125.5 g. There were no statistical differences only with B.396 and York 9. The
biggest fruits of ‘Auksis’ apples were on rootstock Bulboga, though there were no
significant differences with rootstocks M.9, B.491, B.146, M.26 and P 60.
Rootstocks B.491, York 9 and Bulboga produced the lowest percentage of small
fruits (60-65 mm diameter), while Pure 1 the highest. The highest percentage of
75-85 mm fruits was obtained from trees on Bulboga, M.9, B.491 and P 60.
There were found significant differences among rootstocks effect on fruit red
colour. Fruit from trees on rootstocks Pure 1 and P 22 had the highest percentage of
red colour. Rootstock M.26 determined poor colouring of ‘Auksis’ apple fruits.
Fruits on Bulboga had significantly the highest firmness during harvesting. Other
rootstocks did not differ significantly, though fruits on rootstock P 2 were somewhat
softer.
P 2 determined higher content of soluble solids and it differed significantly from
rootstocks B.491, Pure 1, M.26, Bulboga, P 22, B.9, B.146. Lower content of soluble
solids was on B.491, Pure 1, M.26 and Bulboga.
The maturity index indicated that ‘Auksis’ apples were more mature from trees
on rootstock Pure 1, though there were no significant differences with P 22 and P 2.
Bulboga induced later ripening of apples.
259
T a b l e 1. Rootstock effect on average fruit yield per tree and fruit
size (2004–2005)
1
l e n t e l ë.
Rootstock
Poskiepio átaka vidutiniam derliui ir vaisiø kokybei 2004–2005 m.
Average yield,
kg / per tree
Mean fruit
weight
Distribution of fruit size
Vaisiø pasiskirstymas pagal skersmená,
%
Vidutinis derlius,
kg/vaism.
Vidutinë vaisiaus
masë, g
60–65
66–75
P 22
10.68
144.3
10
48
31
11
P2
9.54
145.1
12
58
27
3
M.9
13.30
151.1
8
47
41
4
B.9
12.48
147.1
14
49
31
6
Pure 1
18.10
125.5
22
67
11
0
B.491
11.92
152.1
2
54
43
1
B.146
15.33
153.3
6
56
36
2
York 9
15.46
138.0
4
65
26
5
B.396
10.56
137.7
5
66
29
0
P 60
12.80
157.0
5
43
44
8
M.26
13.68
153.1
8
66
25
1
BULBOGA
15.80
165.5
4
50
46
0
3.47
11.99
Poskiepis
LSD05 / R05
76–85
86–95
Discussion. Mean fruit weight on rootstock P 22 did not differ from other
rootstocks, when in the numerous trials there was established negative effect of
P 22 on fruit weight (Jadczuk, Wlosek-Staugut, 1999; Ystaas, 1993). The results of
fruit size distribution defined wide range of fruit size classes. Rootstock P 22 had the
highest percentage of big size fruits, but at the same time 10% of fruits were smaller
than 65 mm. The same tendencies were obtained with B.9. Mean fruit weight depended
on crop load and tree vigour. High yielding dwarf rootstock Pure 1 produced smallest
fruits, but high yielding semi-dwarf rootstock Bulboga produced biggest fruits. To
state rootstock effect on mean fruit weight is difficult and it was reported by many
researches (Al-Hinai, Roper, 2004; Barden, Marini, 1999). Generally M.26 EMLA
and M.9EMLA result in the largest fruit (Autio et al., 2001; Barden, Marini, 2001),
but it was not confirmed in our trial.
Though there were found significant differences among rootstocks effect on
fruit red colour rootstock had conditional influence on fruit colouring. Similar
tendencies were noted in other rootstock trials, where red colour was variable and it
was impossible to draw general conclusions (Barden, Marini, 2001). Colour mainly
was caused by rootstock effect on crop load, tree vigour and fruit size. Fruits from
weakly growing and highly yielding trees on rootstocks Pure 1 and P 22 had the
highest percentage of red colour. Better colouring of apples on rootstock P 22 was
recorded in Netherlands, too (Maas, Wertheim, 2004). In many trials positive effect
of rootstock M.9 on fruit colour was not established in our investigation. Tendency
260
of poorer colouring increasing rootstock growth vigour was noted. Semi-dwarf
M.26 determined poorest colouring of ‘Auksis’ apple fruits. On the other hand,
fruits from the most vigorous rootstock Bulboga in this trial had good colour. Such
findings once more show the importance of rootstock/variety combination.
T a b l e 2. Rootstock effect on fruit quality and ripening time
(average 2004–2005)
2
l e n t e l ë. Poskiepio átaka vaisiø kokybei ir sunokimo laikui, 2004–2005 m.
vidurkis
Rootstock
Poskiepis
Blush
Nusispalvinimas,
%
Firmness
Minkštimo
kietumas,
Starch conversion,
points
SSC
kg cm-1
Krakmolo
susiskaidymas balais
Tirpios
sausosios
medžiagos, %
Maturity
index
Sunokimo
indeksas
P 22
64
8.2
5.4
12.55
0.12
P2
53
8.0
5.2
13.18
0.12
M.9
51
8.3
4.4
12.86
0.15
B.9
52
8.3
5.1
12.65
0.14
Pure 1
69
8.2
6.3
12.31
0.11
B.491
48
8.5
5.3
12.28
0.15
B.146
48
8.2
4.7
12.71
0.15
York 9
58
8.4
4.6
12.96
0.15
B.396
50
8.4
5.3
12.78
0.13
P 60
56
8.5
4.8
12.85
0.13
M.26
43
8.4
4.9
12.33
0.15
BULBOGA
55
8.7
3.3
12.31
0.22
10.3
0.26
0.50
0.45
0.019
LSD05 / R05
There were no clear differences among rootstocks effect on the content of
soluble solids. P 2 determined higher content, but it was not significantly different
from numerous rootstocks in this trial. Nevertheless, positive effect of P 2 was
established in earlier performed trials (Kviklienë, Kviklys, 2001). Very clear differences
were established in the trial with cultivar ‘Melrose’ comparing dwarf and semidwarf rootstocks. At harvest time fruits on low vigorous rootstocks P 22, M.9 and
P 2 contained much more soluble solids than stronger growing rootstocks M.26 and
P 60 (Kviklys, Kviklienë, 2002). In this study dependence between rootstock growth
vigour and content of soluble solids was not clear.
Rootstock Bulboga had positive effect on fruit flesh firmness. At the same time
starch conversion rate was low. Combination of both factors determined late maturity
of apple fruits on this rootstock. During the harvest fruits on Pure 1 had very high
starch conversion rate, therefore rootstock effect on earlier apple maturation was
established. P series rootstocks induced earlier fruit ripening than B series rootstocks.
261
Conclusions. 1. Rootstock Pure 1 determines high yields, better colouring,
earlier ripening and smallest fruits of cv. ‘Auksis’.
2. Rootstock Bulboga induces big fruits, high firmness and late ripening of
apples.
3. Rootstock P 2 determines higher content of soluble solids and lower firmness.
4. Effects of other rootstocks on fruit quality characters were not stable and
insignificant.
Acknowledgement. This work was partly supported by Lithuanian State Science
and Studies Foundation.
Gauta
2006 06 22
Parengta spausdinti
2006 07 13
References
1. A l - H i n a i Y. K., R o p e r T. R. Rootstock Effects on Growth and Quality
of ‘Gala’ Apples. HortScience. 2004. 39(6). P. 1231-1233.
2. A u t i o W. R., A n d e r s o n J. L., B a r d e n J. A., B r o w n G.
R., C r a s s w e l l e r R. M., D o m o t o P. A., E r b A., F e r r e e D. C.,
G a u s A., H i r s t P. M., M u l l i n s C. A., S c h u p p J. R. Location
affects performance of ‘Golden Delicious’, ‘Jonagold’, ‘Empire’, and ‘Rome Beauty’ apple
trees on five rootstocks over ten years in the 1990 NC-140 cultivar/rootstock trial // Journal
of the American Pomological Society. 2001. 55(3). P. 138-145.
3. B a r d e n J. A., M a r i n i R. P. Yield, Fruit Size, Red Color, and Estimated
Crop Value in the NC-40 1990 Cultivar/Rootstock Trial in Virginia // Journal of the American
Pomological Society. 55. 2001. P. 154-158.
4. B a r d e n J. A. and R. P. M a r i n i. Rootstock effects on growth and
fruiting of a spur-type and a standard strain of ‘Delicious’ over eighteen years. Fruit Var.
J. 1999. 53. P. 115-125.
5. Y s t a a s J., F r o y n e s O. Effects of the Polish rootstocks P2 and P22 on
vigour, yield and fruit characteristics on apple cultivar Gravenstein // Acta Agric.
Scandinavica. 1999. 43. P. 244-246.
6. J a d c z u k E., W l o s e k - S t a u g u t C. R. Cropping and fruit quality
of ‘Jonagold’ apple trees depending on rootstock // Apple rootstocks for intensive orchards
/ Proceedings of international seminar. Warszawa, P. 45-46.
7. Ja g e r A., R o e l o f s F. P. M. M., W e s t e r w e e l e K.,
L i e s h o u t J. Optimum harvest date of apples for direct concumption and for
prolonged storage // Annual Report Wilheminadorp Fruit Research Station. 1996. P. 83-86.
8. K r u c z y n s k a D., C s y n z y k A., B u c z e k M. Effect of rootstock,
weather and soil condition upon growth, cropping and fruit quality of gala Must apple
trees // Apple rootstocks for intensive orchards / Proceedings of international seminar.
Warszawa, 1999. P. 61-62.
9. K v i k l i e n ë N., K v i k l y s D. Obelø vegetatyviniø poskiepiø átaka
‘Jonagold’ ir ‘Melrose’ vaisiø sunokimui ir kokybei // Sodininkystë ir darþininkystë. 2001.
20(1). P. 25-34.
262
10. K v i k l y s D., K v i k l i e n ë N. Effect of rootstock on apple quality and
storability // Folia Horticulture. 2002. 14/1. P. 227-233.
11. M a a s F. M., W e r t h e i m S. J. A multi-site rootstock trial with the
apple cultivars ‘Cox’s Orange Pippin’ and ‘Jonagol’ // Acta Horticulturae. 2004. 658(1). P.
177-184.
12. S k r z y n s k i J. Wstepne wyniki badan nad wplywem wybranych podkladek
karlowych na jakosc owocow jabloni odmiany ‘Jonagold’ //Wsplolczesne trendy w
agrotechnice sadow. Liublin, 1997. P. 41-45.
13. S t r e i f J. Optimum harvest date for different apple cultivars in the ‘Bodensee’
area // In Cost 94. The postharwest treatment of fruit and vegetables. Lofthus. Norway,
1996. P. 15-20.
14. T o m a l a K., A n d z i a k J., K o b u s i n s k i K. Influence of
rootstocks on fruit maturity and quality of ‘Jonagold’ apples // Apple rootstocks for
intensive orchards / Proceedings of international seminar. Warszawa, 1999. P. 13-14.
15. W e b s t e r A. D. New dwarf rootstocks for apple, pear, plum and sweet
cherry – a brief review // Acta Agriculture. 1993. 349. P. 145-153.
16. W e r t h e i m S. J. Rootstock guide. Wilhelminadorp. 1998.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
258–263.
POSKIEPIO ÁTAKA ‘AUKSIO’ VAISIØ KOKYBEI IR NOKIMUI
N. Kviklienë, D. Kviklys
Santrauka
2004–2005 m. Lietuvos sodininkystës ir darþininkystës institute atlikti vegetatyviniø
poskiepiø P 22, P 2, M.9, B.9, Pure 1, B.491, B.146, York 9, B.396, P 60, M.26 ir Bulboga
tyrimai su ‘Auksio’ veislës obelimis. Nustatyta poskiepiø átaka vidutinei vaisiø masei,
dydþiui, nusispalvinimui, vaisiø kokybei ir sunokimui. Didþiausi gauti vaismedþiø su
Pure 1, B.146 ir Bulboga poskiepiais vidutiniai derliai. Maþiausiai vaisiø priskinta nuo
vaismedþiø su maþiausio augumo poskiepiais – P 2, B.396 ir P 22. Vidutinë vaisiaus masë
priklausë nuo derëjimo gausumo ir poskiepio augumo. Gausiai derantys vaismedþiai su
Pure 1 poskiepiu iðaugino smulkiausius vaisius. Didesni vaisiai uþaugo ant vaismedþiø su
augesniu Bulboga bei þemaûgiu M.9 poskiepiu. Spalvingiausi vaisiai uþaugo ant vaismedþiø
su Pure 1 ir P 22 poskiepiais. Tyrimø metais kieèiausius obuolius uþaugino vaismedþiai su
Bulboga poskiepiu, minkðèiausius – su P 2 poskiepiu. Daugiausia tirpiø sausøjø medþiagø
buvo vaismedþiø su P 2 poskiepiu vaisiuose. Pure 1 poskiepis labai paankstino vaisiø
sunokimà. Vëliausiai sunoko vaismedþiø su Bulboga poskiepiu vaisiai.
Reikðminiai þodþiai: Malus x domestica Borkh., poskiepis, sunokimo indeksas, vaisiø
kokybë.
263
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 264–272.
INFLUENCE OF DIFFERENT DWARFING METHODS ON
CONTENT OF MICROELEMENTS IN APPLE TREE
ORGANS
Maciej GÀSTOÙ, Jan SKRZYÑSKI
Department of Pomology and Apiculture, Agricultural University in Kraków,
Al. 29 Listopada 54, 31-425 Kraków, Poland.
E-mail: [email protected]
The paper presents the results of chemical analyses of different organs of apple tree
cv. ‘Jonica’. The trees were dwarfed with: rootstocks (M.9 and P 60), and additionally, with
bark grafting (in normal and inverted position), microinterstocks (M.9, P 22, M.27) and
growth retardant (Paclobutrazol). Microinterstock is an additional way of dwarfing, when
a ring of bark taken from dwarfing rootstock is grafted on the tree’s trunk. In 1996–1999
fruit, leaf, wood, bark and root samples of each treatment were collected and iron, copper
and zinc content analysed by atomic absorption spectroscopy. The highest concentration
of Fe was noted in roots (1271 mg·kg-1 d.w.), lower – in leaves (164 mg·kg-1 d.w.) and the
lowest – in bark, wood and fruit (95, 28, and 22 mg·kg-1 d.w., respectively). The highest
amount of Cu was studied in leaves and bark samples (33.9 mg·kg-1 d.w. and 27.3 mg·kg-1
d.w.), whereas the lowest copper level was found in wood and fruits (4.2 mg·kg-1 d.w. and
3.4 mg·kg-1 d.w.). Mean Zn content varied from 161 mg·kg-1 d.w. (roots) to 7.0 mg·kg-1 d.w.
(wood). As far as leaf microelement content is concerned, used dwarfing method had no
or little effect. However, the great differences between analysed seasons were observed.
Bark analysis revealed that bark grafting and microinterstocks favoured higher microelement
concentrations especially below the place of graft. Bark grafting and microinterstocks
significantly increased root Fe and Zn content (even 6 times as compared with control
trees). Zn content in roots negatively correlated with the vigour of the investigated trees.
Accumulation of Cu in roots was also differentiated, however the differences were not
significant. Root microelement concentration showed a big inter-seasonal variation.
Key words: Malus × domestica Borkh., rootstocks, bark grafting microinterstocks,
bark, leaves, roots, fruit mineral content.
Introduction. Rootstock has a great impact on the growth and yield of fruit
tree. It also shows big differences with respect to the uptake and transport of mineral
elements. However, in some cases, the use of rootstock alone is not sufficient to
reduce tree vigour. Therefore the additional way of dwarfing must be sought. Promising
results with bark grafting or microinterstocks were obtained by Arakawa et al. (1997),
Poniedziaùek et al. (2000) and Gàstoù (2002).
264
The knowledge of specific rootstock/scion – climate – soil interaction is essential
to define their characteristics, e.g. nutritional demands. Therefore, the aim of the
present study was to investigate the influence of different dwarfing method (rootstock,
bark grafting, microinterstock, growth regulator) on microelement content. As some
authors (Hrotko, 2004) suggested more comprehensive holistic approach to
rootstock-scion interaction, we focused not only on usually analyzed parts – leaves
and fruits, but on all other organs, which also take part in the mineral nutrition of
apple tree.
Material and methods. The experiment was established in the spring of 1995
at the Experimental Station in Garlica Murowana, near Krakow. The soil of the plot
where the fruit trees were planted was in the valuation class II b. It was the brown
soil type developed from loess and represented species determined as silt loam. Soil
properties are given in Tables 1 and 2.
T a b l e 1. Granulometric soil content of experimental orchard
1
l e n t e l ë. Bandymø sodo dirvos granuliometrinë sudëtis
Fraction diameter
mm
Percentage of
fraction / Frakcijos
Frakcijos skersmuo,
1,0–01
0.1–0.05
0.05–0,02
0.02–0.006
0.006–0.002
< 0.002
2
10
48
22
5
13
procentas
T a b l e 2. Acidity, macro- and microelement content in soil before
orchard planting (mean values)
2
l e n t e l ë.
Dirvos rûgðtumas, makro- ir mikroelementø kiekis joje prieð
pasodinant sodà (vidurkiai)
Depth of sampling
Ëminio paëmimo gylis, cm
pHKCl
0–20
20–40
5.3
4.9
*
**
Available mineral content
-1
Mineralø kiekis, mg 100 g
P
K
Mg
Ca
4.9*
4.1
10.9*
9.0
6.6**
9.11
36.5
39.8
Fe,
%
Zn,
ppm
Cu,
ppm
1.82
1.73
101
127
23.3
26.4
determined using Egner – Riehm method / nustatyta Egnerio-Riehmo metodu
determined using the universal method / nustatyta universaliu metodu
The experimental material was composed of one-year old budded trees of cultivar
‘Jonica’ on two rootstocks P60 and M.9. Soil cultivation system in the orchard was
herbicidal fallow in rows and grass in inter-rows. Apple trees were spaced at 1.5 ×
3.5 m. The crowns of trees were trained in a slender spindle form. The protection of
the trees was carried out according to the recommendations accepted for commercial
plantations. However, no preventive spraying with calcium salts was applied.
The experiment was established in a randomized blocks design, each treatment
being represented by four replications – plots of five trees per each. The following
treatments were used in the experiment:
1. Control I (=Control/M.9)– apple tree ‘Jonica’ budded on rootstock M.9;
2. Control II (=Control/P60) – apple tree ‘Jonica’ budded on rootstock P 60;
265
3. Grafting with a bark ring in normal position (= Ring 0°) – apple tree ‘Jonica’
budded on P 60; a bark ring taken from the tree trunk was grafted in the same place
with its polarity preserved;
4. Grafting with a bark ring in an inverted position (= Ring 180°) – apple tree
‘Jonica’ on rootstock P 60; a bark ring taken from a tree was inverted by 180° and
grafted in an inverted position;
5. Microinterstock M.9 – apple tree ‘Jonica’ on rootstock P 60; a bark ring
taken from the trunk was replaced with a bark ring from rootstock M.9 in the
normal position;
6. Microinterstock P 22 – apple tree ‘Jonica’ on rootstock P 60; a bark ring
taken from the tree trunk was replaced with a bark ring from rootstock P 22 in the
polar position;
7. Microinterstock M.27 – apple tree ‘Jonica’ on rootstock P60; a bark ring
taken from the tree trunk was replaced with bark ring from rootstock M.27;
8. Paclobutrazol – apple tree ‘Jonica’ on rootstock P 60; Paclobutrazol (Cultar)
applied to the root neck in spring. No microinterstock.
In May of 1996 in treatments 3–7 bark rings of 2 cm in width were grafted.
The grafting was carried out on the whole circumference of trunk at the height of
40 cm. The treatment was conducted only in 1996 while every year in the same
period Cultar (20 mg/l) was applied to the root necks of trees in the form of a lanolin
ointment.
Fruit and leaf samples for chemical analysis were taken directly from the trees
growing in the experimental orchard while the samples of roots, bark and wood
were taken from trees, which were purposefully planted on additional reserve plots.
Each treatment was represented by eight samples.
Tree roots were sampled during the period of tree rest (late autumn). The collected
material was washed in tap water to remove soil, then rinsed in distilled water and
dried. At the same time the samples of bark* and wood were separately taken from
below and above the microinterstocks. Leaf samples were collected in the last 10
days of July. From each plot a sample of 100 leaves with petioles and stipules was
taken from a middle part of long shoots. From each plot 25 apples were also sampled,
their flesh cut in thin slices and dried at 60°C. Then all the samples were ground in
a beater mill.
The prepared air dry samples were subjected to wet mineralization in a mixture
of nitric and perchloric acids (at ratio 3:1) and their composition was assessed using
an atomic absorption spectrometer (AA 140, Varian).
The measurements were listed and subjected to analysis of variance. Differences
between the means were ascertained with a multiple Duncan Test, using a Statistica
6.0 program. The mean values for the combinations labeled with the same letters do
not significantly differ at the significance level α = 0.05.
The word “bark” was used for all tissues located in the trunk outside of cambium
and constituting the secondary bark. It includes phloem, parenchyma of core rays and
multi-annual peryderma.
*
266
Results and discussion. The distribution of mineral constituents in the plant is
irregular (Parups et al., 1958; Mason and Whitfield, 1960; Ford, 1966; Martin et al.,
1970; Baghdadi and Sadowski, 1998). This was confirmed in the present study and
was obviously due to the different functions of the particular fruit tree organs
(Table 3).
T a b l e 3. Mean iron, zinc and copper content in different organs of
apple tree
3
l e n t e l ë.
Vidutinis geleþies, cinko ir vario kiekis skirtingose obelø
vaismedþiø dalyse
Fe (mg kg-1 d.m.)
Fruits / Vaisiai
Leaves / Lapai
Wood / Mediena
Bark / Þievë
Roots / Šaknys
Zn (mg kg-1 d.m.)
22 a*
164 b
28 a
95 ab
1271 c
10 a
37 b
7a
47 b
161 c
Cu (mg kg-1 d.m.)
3a
34 c
4a
27 c
17 b
* Means followed by the same letter do not differ at α = 0.05; Duncan’s Multiply Range Test /
Ta paèia raide paþymëtos reikðmës pagal Dunkano kriterijø (α = 0,05 ) nesiskiria.
Dwarfing method had no effect on leaf and fruit iron content (Tables 4 and 5).
However, big differences between analyzed tree organs were found. Similar Fe
distribution reported Wendt (1972), however, he found low iron content measured
in roots. The reverse was true for this study, mean root Fe content reached
1271 ppm. The similar values (800 ppm) noted Baghdadi and Sadowski (1998).
T a b l e 4. Influence of different dwarfing methods on iron, zinc and
copper content (mg kg-1 d.m.) in fruits in 1997–1999
4
l e n t e l ë.
Skirtingø augimà stabdanèiø metodø átaka geleþies, cinko ir vario
kiekiui (mg kg -1 s.m.) vaisiuose 1997—1999 m.
Treatment / Variantas
Control/M.9
Fe (mg kg-1 d.m.)
Zn (mg kg-1 d.m.)
Cu (mg kg-1 d.m.)
18.5 a
5.9 a
3.6 abc
22.1 ab
5.9 a
3.8 c
Ring of bark 0°
31.4 b
19.8 a
3.7 bc
Ring of bark 180°
19.5 a
5.0 a
3.1 a
19.0 a
5.7 a
3.2 ab
19.3 a
19.4 a
3.1 a
17.7 a
6.1 a
3.0 a
24.3 ab
17.1 a
3.1 ab
Kontrolinis variantas/M.9
Control/P 60
Kontrolinis variantas/P 60
Þievës þiedas 0°
Þievës þiedas 180°
Microinterstock M.9
Mikrointarpas M.9
Microinterstock P 22
Mikrointarpas P 22
Microinterstock M.27
Mikrointarpas M.27
Paclobutrazol
267
T a b l e 5. Influence of different dwarfing methods on iron, zinc and
copper content (mg kg-1 d.m.) in leaves in 1996–1998
5
l e n t e l ë. Skirtingø augimà stabdanèiø metodø átaka geleþies, cinko ir vario
kiekiui (mg kg -1 s.m.) lapuose 1996–1998 m.
Fe (mg kg-1 d.m.)
Zn (mg kg-1 d.m.)
Cu (mg kg-1 d.m.)
161 a
37.4 a
32.5 a
163 a
35.6 a
31.9 a
Ring of bark 0°
166 a
35.3 a
36.8 a
Ring of bark 180°
157 a
37.6 a
33.7 a
149 a
37.7 a
33.8 a
185 a
40.4 a
35.0 a
158 a
37.7 a
31.8 a
175 a
37.0 a
35.4 a
Treatment / Variantas
Control/M.9
Kontrolinis variantas/M.9
Control/P 60
Kontrolinis variantas/P 60
Þievës þiedas 0°
Þievës þiedas 180°
Microinterstock M.9
Mikrointarpas M.9
Microinterstock P 22
Mikrointarpas P 22
Microinterstock M.27
Mikrointarpas M.27
Paclobutrazol
.
T a b l e 6. Influence of different dwarfing methods on iron, zinc and
copper content (mg kg-1 d.m.) in wood of apple trees in
1996–1998
6
l e n t e l ë. Skirtingø augimà stabdanèiø metodø átaka geleþies, cinko ir vario
kiekiui (mg kg -1 s.m.) obelø medienoje 1996–1998 m.
Treatment / Variantas
Control/P60
Kontrolinis variantas/P 60
Ring of bark 0°
Þievës þiedas 0° ⇑**
Ring of bark 0°
Þievës þiedas 0° ⇓
Ring of bark 180°
Þievës þiedas 180°⇑
Ring of bark 180°
Þievës þiedas 180°⇓
Microinterstock M.9
Mikrointarpas M.9 ⇑
Microinterstock M.9
Mikrointarpas M.9 ⇓
Microinterstock P 22
Mikrointarpas P 22 ⇑
Microinterstock P 22
Mikrointarpas P 22 ⇓
Microinterstock M.27
Mikrointarpas M.27 ⇑
Microinterstock M.27
Mikrointarpas M.27 ⇓
Fe (mg kg-1 d.m.)
Zn (mg kg-1 d.m.)
Cu (mg kg-1 d.m.)
60.5 bc
5.2 ab
4.5 b
15.6 a
6.0 ab
3.7 a
19.6 a
7.0 ab
3.8 a
17.5 a
5.1 ab
4.1 ab
17.9 a
7.1 b
3.9 ab
62.8 c
6.9 ab
3.9 ab
30.5 ab
9.7 c
3.6 a
21.6 a
4.8 a
4.6 b
24.6 a
8.8 bc
4.3 ab
22.9 a
6.6 ab
4.7 b
32.6 ab
9.0 bc
4.7 b
**⇑ - sample taken above the site of grafting / ëminys paimtas virð skiepo vietos
⇓ - sample taken below the site of grafting / ëminys paimtas þemiau skiepo vietos
268
Mean zinc and copper content was in accordance with results noted by Ostrowska
et al. (1991). Used treatments, had no or little effect on leaf and fruit Zn content.
Fruit zinc content showed big inter-seasonal variation (data not shown). The highest
valued were recorded for 1998; it was probably caused by intensive pesticide usage.
Many authors reported higher microelement content measured in bark in
comparison to wood (Taylor, 1967; Zelenskaja and Èernij, 1966; Kropp et al., 1981;
Wendt, 1971; Ford, 1966, Høivna et al., 1989; Hluðek et al., 1989). This study
confirmed it in respect to zinc and copper; values for Fe were not significantly
different.
Dwarfing methods strongly influenced mineral content in all investigated organs.
This was especially evident in the first year of study. During following years this
effect diminished. All microinterstocks increased Fe content in bark when samples
were taken below the place of grafting (Table 7). There was only exception –
T a b l e 7. Influence of different dwarfing methods on iron, zinc and
copper content (mg kg-1 d.m.) in bark of apple trees in
1996–1998
7
l e n t e l ë. Skirtingø augimà stabdanèiø metodø átaka geleþies, cinko ir vario
kiekiui (mg kg -1 s.m.) obelø þievëje 1996–1998 m.
Treatment / Variantas
Control/P 60
Kontrolinis variantas/P 60
Ring of bark 0°
Þievës þiedas 0° ⇑
Ring of bark 0°
Þievës þiedas 0° ⇓
Ring of bark 180°
Þievës þiedas 180° ⇑
Ring of bark 180°
Þievës þiedas 180° ⇓
Microinterstock M.9
Mikrointarpas M.9 ⇑
Microinterstock M.9
Mikrointarpas M.9 ⇓
Microinterstock P 22
Mikrointarpas P 22 ⇑
Microinterstock P 22
Mikrointarpas P 22 ⇓
Microinterstock M.27
Mikrointarpas M.27 ⇑
Microinterstock M.27
Mikrointarpas M.27 ⇓
Fe (mg kg-1 d.m.)
Zn (mg kg-1 d.m.)
Cu (mg kg-1 d.m.)
91 ab
29.4 a
6.7 a
81 a
37.7 b
23.4 bc
101 b
45.0 b
22.8 bc
85 a
41.3 b
34.4 c
108 b
49.5 c
23.7 bc
78 a
35.1 b
20.8 b
95 ab
62.9 d
19.6 b
81 a
24.0 a
26.6 bc
110 b
58.6 cd
31.8 bc
104 b
51.6 c
48.7 d
104 b
67.7 d
26.2 bc
microinterstock M.27. The same tendency was proved for zinc (exception: ring of
bark 0°) Microinterstocks favoured higher root Fe and Zn content (Table 8). The
same was true for bark graft, especially for ring of bark grafted in an inverted
position. This treatment especially increased root Fe content (1556 ppm) and
Zn (212 ppm), whereas for non-treated trees mean values was 563 ppm and
269
30 ppm, respectively. Obtained values are much higher than reported by Ford (1966)
and Baghdadi and Sadowski (1998). The most interesting fact is that vigour of trees
is negatively correlated with root Zn content. The same tendency we investigated in
respect to different dwarfing apple rootstocks (Skrzyñski and Gàstoù, 2005).
T a b l e 8. Influence of different dwarfing methods on iron, zinc and
copper content (mg kg-1 d.m.) in roots of apple trees
in1996–1998
8
l e n t e l ë.
Skirtingø augimà stabdanèiø metodø átaka geleþies, cinko ir vario
kiekiui (mg kg -1 s.m.) obelø ðaknyse 1996–1998 m.
Treatment / Variantas
Control/P 60
Kontrolinis variantas/P 60
Ring of bark 0°
Þievës þiedas 0°
Fe (mg kg-1 d.m.) Zn (mg kg-1 d.m.) Cu (mg kg-1 d.m.)
563 a
30 a
9.7 a
859 ab
127 b
15.7 a
Ring of bark 180°
1556 c
212 d
20.1 a
Microinterstock M.9
1115 bc
163 bcd
13.0 a
1445 c
139 bc
18.4 a
1379 c
190 cd
21.7 a
Þievës þiedas 180°
Mikrointarpas M.9
Microinterstock P 22
Mikrointarpas P 22
Microinterstock M.27
Mikrointarpas M.27
According to Cutting and Lyne (1993), due to girdling and reducing phloem
transport, root activity and development was reduced. The capacity to uptake some
elements decreased. This probably could change the balance in the content of elements
in roots. Another explanation is lower dilution of microelements in smaller root system.
Conclusions. 1. The highest amounts of iron and zinc were measured in roots,
whereas the highest level of Cu was investigated in leaves and bark samples.
2. Additional dwarfing methods significantly influenced mineral content in all
investigated apple tree parts.
3. Zn content in roots negatively correlated with the vigour of investigated
trees.
Gauta
2006 06 22
Parengta spausdinti
2006 08 04
270
References
1. A r a k a w a O., K a n n o K., K a n e t s u k a A., S h i o z a k i Y.,
B a r r i t t B., K a p p e l F., 1997. Effects of girdling and bark inversion on tree
growth and fruit quality of apple. Acta Hort. 451, 579–585.
2. B a g h d a d i M., S a d o w s k i A., 1998. Concentration of mineral elements
in different parts of ‘Schattenmorelle’ cherry trees on Prunus avium seedling stock. [in:]
Proc. 3rd Int. Cherry Symp., Acta Hort., 468, 523–528.
3. C u t t i n g J. G. M., L y n e M. C., 1993. Girdling and the reduction in shoot
xylem sap concentrations of cytokinins and gibberelins in peach. J. Hort. Sci., 68, 619–626.
4. F o r d E., 1966. Studies in the nutrition of apple rootstocks. III. Effect of level of
magnesium nutrition on growth, form and mineral composition. Ann. Bot. N.S., 30, 639–655.
5. G à s t o ù M. 2002. Effect of different dwarfing methods on growth, fruiting and
mineral content of apple tree. Ph.D. Thesis, A.R. w Krakowie, 136 str.
6. H l u ð e k J., H a v e l k a B., H ø i v n a L., 1989. Obsah fosforu a vapniku
v organech nehnojenych jabloni odrudy Gloster 69. Acta Universitatis Agriculturae,
Facultas Horticulturae, 4, 27–39. Hort. Abstr. vol. 62/1823.
7. H ø i v n a L., H a v e l k a B., H l u ð e k J., 1989. Obsah drasliku a horièku
v organech nehnojenych jabloni odrudy Gloster 69. Acta Universitatis Agriculturae,
Facultas Horticulturae, 4,13–26. Hort. Abstr. vol. 62/1817.
8. H r o t k o K., 2004. Advances and challenges in fruit rootstock research. 8th
Intern. Symposium on Integrating Canopy, Rootstock and Environmental Physiology in
Orchard Systems, Budapest 13–18 June, 27.
9. K r o p p K., B e n J., P o n i e d z i a ù e k W., N o s a l K., 1981.
Nitrogen, phosphorus, potassium and dry matter content in trunks of apple cvs. ‘Jonathan’
and ‘Cox Orange’ grown on different rootstocks (in Polish). Zesz. Nauk. A.R. Kraków, 163,
99–110.
10. M a r t i n D., L e w i s T. L., C e r n y J., G r a s s i a A., 1970. Effect
of high levels of nitrogen on mineral content and disorder incidence in Jonathan apples
in pot culture. CSIRO Austr. Div. Pl. Techn. Paper 29. [in:] L.S. Jankiewicz (red.) Fizjologia
roúlin sadowniczych. PWRiL, Warszawa, 208–233.
11. M a s o n
A. C., W h i t f i e l d A. B., 1960. Seasonal changes in the
uptake and distribution of mineral elements in apple trees. J. Hort. Sci., 35, 34–55.
12. O s t r o w s k a A., G a w l i ñ s k i S., S z c z e b i a ù k a Z., 1991.
Metody analizy i oceny wùaúciwoúci gleb i roúlin. Instytut Ochrony Úrodowiska, Warszawa.
13. P a r u p s E., K e n w o r t h y A. L., B e n n e E. J., B a s s S. T.,
1958. Growth and composition of leaves and roots of Montmorency cherry trees in relation
to sulfate and chloride supply in nutrient solutions. Proc. Amer. Soc. Hort. Sci, 71, 135–144.
14. P o n i e d z i a ù e k W., P o r æ b s k i S., R z e ê n i c k a B., 2000. Effect
of bark grafting on growth and flower bud formation on young apple trees in the nursery.
Folia Hort. 12/2: 63–68.
15. S k r z y ñ s k i J., G à s t o ù M., 2005. Zawartoúã C-organicznego i
skùàdników mineralnych w korzeniach podkùadek jabùoni polskiej hodowli. [in:] Michalik
B., Ýurawicz E. (eds.) Zmiennoúã genetyczna i jej wykorzystanie w hodowli roúlin
ogrodniczych, IsiK, Skierniewice: 293–298.
16. T a y l o r B. K., 1967. Storage and mobilization of nitrogen and fruit trees. J.
Aust. Agric. Sci, 33, 23–29.
17. W e n d t T., 1972. Untersuchungen über Haupt –u. Spurennährstoff-gehalte
in Ausdauernden Baumteilen von Cox Orange auf M IV. Erwerobstbau, 14, 148–151.
18. Z e l e n s k a j a J. D., È e r n i j A. M., 1966. Osobiennost postuplienja
a rasriedanija 32P w jabùonie. Siel. Choz. Biaù, 1, 576–582.
271
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
264–272.
SKIRTINGØ AUGIMÀ STABDANÈIØ METODØ ÁTAKA MIKROELEMENTØ
KIEKIUI OBELYSE
M. Gàstoù, J. Skrzyñski
Santrauka
Straipsnyje pateikti ‘Jonica’ veislës obelø skirtingø vaismedþiø daliø biocheminës
analizës rezultatai. Vaismedþiø augimas buvo stabdytas panaudojant M.9 ir P 60 poskiepius,
papildomai skiepijant þievës þiedu (normali ir atvirkðtinë padëtis), mikrointarpais (M.9,
P 22, M.27) ir purðkiant augimo retardantu (Paclobutrazol). Mikrointarpas yra papildomas
augimo stabdymo bûdas, kai nuo þemaûgio poskiepio nupjaunamas þievës þiedas ir
áskiepijamas á vaismedþio kamienà. 1996–1999 metais buvo paimti kiekvieno varianto vaisiø,
lapø, medienos, þievës ir ðaknø bandiniai ir atominës absorbcijos spektroskopu nustatytas
geleþies, vario bei cinko kiekis juose. Didþiausia geleþies koncentracija buvo ðaknyse
(1271 mg·kg-1 s.m.), maþesnë – lapuose (164 mg·kg-1 s.m.) ir maþiausia – þievëje, medienoje
ir vaisiuose (atitinkamai 95, 28 ir 22 mg·kg-1 s.m.). Daugiausia vario rasta lapø ir þievës
bandiniuose (33.9 mg·kg-1 s.m. ir 27.3 mg·kg-1 s.m.), maþiausiai – medienoje ir vaisiuose
(4.2 mg·kg-1 s.m. ir 3.4 mg·kg-1 s.m.). Vidutinis cinko kiekis ávairavo nuo 161 mg·kg-1 s.m.
(ðaknyse) iki 7.0 mg·kg-1 s.m. (medienoje). Mikroelementø kiekiui lapuose augimo stabdymo
metodas neturëjo átakos arba ji buvo nereikðminga. Taèiau labai skirtingi duomenys gauti
skirtingais metø laikais. Þievës analizë parodë, kad skiepijimas þievës þiedu ir mikrointarpai
lëmë didesnæ mikroelementø koncentracijà, ypaè þemiau skiepo vietos. Skiepijimas þievës
þiedu ir mikrointarpai reikðmingai padidino geleþies ir cinko kieká ðaknyse (net 6 kartus,
palyginti su kontroliniais vaismedþiais). Cinko kiekis ðaknyse neigiamai koreliavo su tirtø
vaismedþiø augumu. Vario kaupimasis ðaknyse irgi buvo diferencijuotas, taèiau skirtumai
nereikðmingi. Mikroelementø koncentracija ðaknyse skirtingais metø laikais labai skyrësi.
Reikðminiai þodþiai: Malus × domestica Borkh., poskiepiai, þievës skiepo
mikrointarpai, þievë, lapai, ðaknys, mineralø kiekis vaisiuose.
272
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 273–282.
CADMIUM RESISTANCE OF APPLE ROOTSTOCKS M.9
AND B.396 IN VITRO
Jurga SAKALAUSKAITË1, Graþina STANIENË1,
Vidmantas STANYS1, Povilas DUCHOVSKIS1,
Giedrë SAMUOLIENË 1, Kæstutis BARANAUSKIS 1,
Akvilë URBONAVIÈIÛTË1, Viktor REVIN2,
Aleksandr LUKATKIN2
1
Lithuanian Institute of Horticulture, LT-54333 Babtai, Kaunas distr.
Lithuania. E-mail: [email protected]
The Mordovia N.P. Ogariov State University, Botany and Plant Physiology
Department, Bolshevistskaja str., 68, Saransk, Russia.
E-mail: [email protected]
2
The aim of the study was to evaluate the impact of cadmium ions on growth of appletree rootstocks M.9 and B.396, photosynthesis apparatus development and synthesis of
carbohydrates in vitro. Cadmium ions hindered the microshoots growth of rootstock M.9
more as compared to rootstock B.396. Statistically significant decrease in chlorophyll a
was determined in the leaves, when inconsiderable amount of CdSO4 was added into the
growth medium. Chlorophyll b and carotenoids content in the microshoot leaves depended
on cadmium content in the growth medium and genetic nature of rootstocks. Cadmium
induced accumulation of fructose and sucrose in the leaves of both rootstocks.
Furthermore, synthesis of maltose was initiated in the microshoot leaves of rootstock M.9
when 10 ìM CdSO4 was added into the growth medium, while glucose, galactose and
maltose were being accumulated, when rootstock B.396 was treated with 5 and 10 µM
CdSO4. Rootstocks M.9 and B.396 responded differently to cadmium impact. Cadmium
had greater impact on microshoot growth, pigment content and sugar alternation in leaves
of rootstock M.9 than B.396.
Key words: cadmium (Cd), in vitro, mono- and disacharide, pigment, rootstock M.9
and B.396.
Introduction. Toxic metals affect various morphological, physiological and
biochemical processes in plants. The most pronounced effect of heavy metals on
plant development is the inhibition of growth (Davies 1991; Ouzounidou et al.1997;
Pahlsson 1990). Exposure to almost any heavy metal, including cadmium, results in
visible symptoms of injury that can be directly linked to the inhibition of
photosynthesis, respiration, and restricted water and nutrient uptake (Costa and Morel
273
1994; Sanita di Topi and Gabbrielli, 1999). Toxic levels of cadmium ions inhibit the
activity of many enzymes, particularly those involved in photosynthesis (Van Assche
and Clijsters 1990; Chugh and Sawhney, 1999; Krupa, 1999), decrease the chlorophyll
content (Somashekaraiah et al., 1992) and cause an oxidative stress (Stroiski and
Kozlowska 1997; Stohs et al., 2000; Sandalio et al., 2001).
The inhibition of photosynthesis by Cd is well documented. It is therefore
reasonable to expect effects on the sugars formation. But at present, information
about the effects of Cd on carbohydrate content and distribution is not clear (Moya
et al. 1993). Greger and Bertell (1992) showed that the contents of sugars in sugar
beet roots and shoots decreased in Cd-treated plants. On the other hand, Greger et
al. (1991) found that Cd supplies either decreased or increased the contents of soluble
sugars and starch in sugar beets depending on the manner in which nutrients and Cd
were supplied to the plants.
One of the indicators, which allow to establish plant adaptation possibilities,
can be photosynthesis apparatus activity and the photosynthetic pigment content in
plant leaves. It is determined that Cd reduces chlorophyll accumulation in leaves
(Lagriffoul et al., 1998; Sarvari, 1999), and carotenoids are less sensitive to Cd
impact (Neelu et al., 2000).
In vitro system can be a proper model applied in investigation of contaminant
substances impact on horticultural plants.
The aim of the study – to estimate the impact of Cd ions on apple tree rootstocks
M.9 and B.396 regeneration, photosynthesis apparatus development and carbohydrates
synthesis in vitro.
Materials and methods. Two apple-tree rootstocks M.9 and B.396 were used
in experiment. Shoots were taken from in vitro culture, grown in Murashige and
Skoog (1962) growth medium supplemented with 4.4 mM 6-benzilaminopurine
(6-BAP) and 3% sucrose. Microshoots were replanted into the same growth medium
with different amount of CdSO4 – 2.5; 5; 10; 25; 50; 100; 200; 500; 1000; 1500;
2000 ìM. A photoperiod of 16 h was used. Light flux at 50 mmol m-2s-1 and air
temperature at 21-25 oC was maintained throughout the experiment. LF-type
luminescence lamps were used for illumination. A total of 32 explants were used per
4 replicates treatment.
Microshoots were grown for one month in the growth medium with different
CdSO4 content, and then evaluation of shoot growth, morphogenesis, colour of
leaves and chemical analysis were performed. Chlorophyll a, b and carotenoids content
per mass unit of green foliage were measured in 100% acetone extract prepared
according to Wettstein method (Wettstein, 1957) using Genesys 6 spectrophotometer
(ThermoSpectronic, USA). Measurements were done in three replicates. To estimate
mono- and disacharide content samples were prepared as follows: 1-2 g of fresh
tissue per sample was ground and diluted with 4 mL bidistilled water. The samples
were pre-purified using 0.2 µm syringe filters. Analysis of fructose, glucose, galactose,
sucrose and maltose was performed on a Shimadzu HPLC system (model 10A)
equipped with refractive index detector (RID 10A), column oven (CTO-10AS VP),
degasser (DGU-14A) and pump (LC-10AT VP). Separations and the determinations
were performed on an Adsorbosil NH2-column (150mm x 4.6mm). Mobile phase:
274
70% acetonitrile. Flow rate: 1mL/min. Measurements were done in five replicates.
All data were analyzed by ANOVA for MS Excel v. 3.43 Fisher’s LSD test
procedure (Pd”0.05)).
Results. Growth of rootstock M.9 shoots was not affected by low
(2.5-5.0 µM) CdSO4 concentrations. However, 10-100 µM amounts of CdSO4 resulted
in significant depression of microshoots growth, while total growth inhibition was
observed under 200-2000 µM of CdSO4 (Table 1). Suchlike growth dependence on
CdSO4 amount was determined for rootstock 62-396 as well, thought no growth
alteration occurred under 10 µM (Table 2).
T a b l e 1. The shoot growth of apple-tree rootstock M.9 under
different content of CdSO4 in the growth medium in vitro
1
l e n t e l ë. Obelø poskiepio M.9 ûgliø augimas, esant skirtingoms CdSO 4
koncentracijoms augimo terpëje in vitro
CdSO4
concentration
koncentracija,
ìM
Shoot
Shoot length Shoots with Shoots with
number
Shoots with
after one green leaves green-brown
brown leaves after one
leaves
Ûgliai
su
month
month
Pasodintø
Ûgliai su þaliai Ûgliai su rudais
Ûgliø ilgis po žaliais lapais,
Ûgliø
rudais lapais,
ûgliø ilgis,
lapais, %
%
skaièius po
mën., mm
mm
%
mën., %
Planted
shoot
length
0 (control /
7.56±0.56 14.13±1.21
pH 5.98)
kontrolë
100
0
0
287.5
2.5
9.50±0.33 13.31±0.76
100
0
0
262.5
5.0
8.44±0.48 13.50±1.21
68.7
31.2
0
281.2
10
9.19±0.49
9.25±0.48
0
100
0
100
25
7.38±0.47
7.38±0.47
0
100
0
100
50
8.94±0.64
9.56±0.64
0
62.5
37.5
100
100
8.44±0.59
8.50±0.62
0
31.3
68.7
100
200
8.56±0.52
8.56±0.52
0
50.0
50.0
100
500
8.75±0.62
8.75±0.65
0
12.5
87.5
100
1000
8.06±0.52
8.06±0.52
0
6.3
93.7
100
1500
8.69±0.56
8.69±0.56
0
0
100
100
2000
7.88±0.54
7.88±054
0
0
100
100
The shoot number doubled in Cd-free medium after a month of in vitro growth.
The number of shoots somewhat increased under low amounts (2.5-5.0 µM) of
CdSO 4 as well. Shoot proliferation was fully suppressed whenever CdSO 4
concentration exceeded 10 µM. At 14 day after replanting microshoot leaves turned
yellow under 2.5-5.0 µM and turned brown under >10 µM amounts of CdSO4. One
month exposure to low and average amounts of CdSO4 resulted in overall brownish
275
green or brown foliage, except for M.9 rootstock, which remained healthy green
under 2.5µM CdSO4 concentration. However, almost all microshoots died after a
month if grown under 500-2000 µM CdSO4 concentrations (Table 1, 2).
T a b l e 2. The shoot growth of apple-tree rootstock B.396 under
different content of CdSO4 the growth medium in vitro
2
l e n t e l ë.
CdSO4
concentration
koncentracija,
ìM
Obelø poskiepio B.396 ûgliø augimas, esant skirtingoms CdSO 4
koncentracijoms augimo terpëje in vitro
Shoots with
Shoot
Shoot length
number
greenShoots with
Shoots with
after one
brown
green leaves
brown leaves after one
month
leaves
month
Ûgliai su þaliais
Ûgliai su rudais
Pasodintø
Ûgliø ilgis po
Ûgliai su
Ûgliø
ûgliø ilgis,
lapais, %
lapais, %
žaliai rudais
skaièius po
mën., mm
mm
lapais, %
mën., %
Planted
shoot
length
0 (control /
5.69±0.41 11.44±1.06
5.98)
kontrolë pH
100
0
0
206.2
2.5
6.69±0.25 15.31±1.65
81.3
18.7
0
218.7
5.0
7.38±0.46 12.75±0.90
25.0
75.0
0
168.7
10
7.75±0.42 10.58±0.65
37.5
62.5
0
118.7
25
7.88±0.41
7.88±0.41
0
100
0
100
50
5.69±0.44
5.75±0.42
0
25.0
75.0
100
100
5.44±0.36
5.56±0.40
0
25.0
75.0
100
200
6.19±0.54
6.19±0.54
0
12.5
87.5
100
500
5.44±0.29
5.44±0.29
0
0
100
100
1000
6.13±0.38
6.13±0.38
0
0
100
100
1500
5.06±0.43
5.06±0.43
0
0
100
100
2000
5.50±0.38
5.50±0.38
0
0
100
100
The shoot number doubled in Cd-free medium after a month of in vitro growth.
The number of shoots somewhat increased under low amounts (2.5-5.0 µM) of
CdSO 4 as well. Shoot proliferation was fully suppressed whenever CdSO 4
concentration exceeded 10 µM. At 14 day after replanting microshoot leaves turned
yellow under 2.5-5.0 µM and turned brown under >10 µM amounts of CdSO4. One
month exposure to low and average amounts of CdSO4 resulted in overall brownish
green or brown foliage, except for M.9 rootstock, which remained healthy green
under 2.5 µM CdSO4 concentration. However, almost all microshoots died after a
month if grown under 500-2000 µM CdSO4 concentrations (Table 1, 2).
In general, cadmium decreased chlorophyll a content in the leaves of apple-tree
rootstocks M.9 and B.396. Significant decrease in chlorophyll a content was observed
under all Cd levels in the leaves of treated microshoots, except for rootstock B.396,
276
where no significant changes were determined under 25 µM amount of CdSO4
(Table 3).
T a b l e 3. Photosynthetic pigment content in the leaf tissue of
apple-tree rootstock M.9 and B.396 under different CdSO4
concentration in the growth medium in vitro
3
l e n t e l ë.
CdSO4
concentration
koncentracija,
Obelø poskiepiø M.9 ir B.396 fotosintetiniø pigmentø kiekis
lapuose, esant skirtingoms CdSO 4 koncentracijoms augimo terpëje
in vitro
Photosynthetic pigment content / Fotosintetiniø pigmentø kiekis, mg g-1 FW
a
µM
b
carotenoids
karotinoidai
a/b
a
rootstock / poskiepis M.9
b
carotenoids
karotinoidai
a/b
rootstock / poskiepis B.396
Control/Kontrolë
2.5
5
10
25
50
100
200
1.06
0.76
0.63
0.85
0.46
0.50
0.28
0.36
0.36
0.30
0.25
0.35
0.17
0.21
0.13
0.16
0.33
0.24
0.22
0.28
0.18
0.22
0.11
0.12
3.00
2.55
2.50
2.39
2.63
2.40
2.21
2.25
1.65
1.28
1.30
1.08
1.46
1.38
1.32
0.93
0.58
0.45
0.45
0.35
0.52
0.54
0.52
0.37
0.51
0.39
0.41
0.35
0.48
0.47
0.47
0.34
2.84
2.86
2.92
3.06
2.80
2.58
2.53
2.52
LSD05 / R05
0.18
0.07
0.06
0.38
0.25
0.09
0.08
0.19
Suchlike impact of Cd ions on chlorophyll b content in the leaves of both
rootstocks was observed as well. The greatest amounts of chlorophyll b was
determined in rootstocks M.9 and B.396 control microshoots, 0.36 and 0.58 mg g-1
of fresh weight (FW) on average, respectively. However, no significant differences
from control plants were determined in the leaves of M.9 rootstock under 2.5 and
10 µM and in the leaves of rootstock B.396 under 25-100 µM Cd levels (Table 3).
In general, chlorophylls a to b ratios dercreased with increasing CdSO4
concentration in the leaves of rootstock M.9. Furthermore, all treatments resulted in
significant decrease of such ratio, except for 25 µM Cd treatment. In the case of
rootstock B.396, greater chlorophylls a to b ratios were observed in the control
plants as well as under 2.5-25 µM CdSO4 concentrations than for those treated with
other amounts of Cd (Table 3).
The greatest amounts of carotenoids were determined in control plants of
rootstocks M.9 and B.396 as well. 0.33 and 0.51 mg g-1 FW on average, respectively.
However, no significant differences from control plants were observed in
25-100 µM Cd-treated B.396 rootstock plant leaves, while Cd treatment of M.9
rootstock plants resulted in significant decrease in carotenoids content under all, but
10 µM amount of CdSO4 (Table 3).
Low amounts of CdSO4 induced the accumulation of fructose and sucrose in
rootstock M.9 microshoots leaves, while glucose or galactose was not detected.
Accumulation of maltose occurred if amount of CdSO4 have exceeded 10 µM. Cd
277
induced the accumulation of fructose and sucrose in rootstock B.396 leaves tissue
as well. Furthermore, low amounts of glucose, galactose and maltose were determined
in microshoots leaves grown under 2.5 and 5 µM CdSO4 (Table 4).
T a b l e 4. Sugars synthesis in the leaf tissue of apple-tree
rootstocks M9 and B.396 under different CdSO4
concentration in the growth medium in vitro
4
l e n t e l ë. Cukrø sintezë obelø poskiepiø M.9 ir B.396 lapuose, esant
skirtingoms CdSO 4 jonø koncentracijoms augimo terpëje in vitro
CdSO4 concentration
koncentracija, ìM
Sugars concentration / Cukrø kiekis, mg g-1
fructose
glucose
galactose
sucrose
maltose
fruktozë
gliukozë
Gglaktozë
sacharozë
maltozë
Rootstock / Poskiepis M.9
Control / Kontrolë
0.38
0
0
0.20
0
2.5
5
10
10.24
8.71
9.28
0
0
0
0
0
0
3.48
3.10
3.65
0
0
1.46
Control / Kontrolë
2.5
5
25
50
5.61
16.99
16.19
13.79
11.59
1.55
9.45
8.08
4.33
1.09
0
0.19
0.13
0
0
Rootstock / Poskiepis B.396
0
0
0.14
0.25
0.15
0.48
0
0
0
0
Discussion. It was well established that high internal Cd concentration disturbed
almost all physiological processes in plants (Barcelo and Poschenrieder, 1990; Van
Asshe and Clijsters, 1990; Krupa and Baszynski, 1995; Siedlecka, 1995). Cd inhibits
the photosynthetic rate as the extent of Cd toxicity depends on applied concentration,
features of species or cultivars, the age of leaves and the stage of plant development
(Baszynski et al., 1980; Becerril et al., 1989; Costa and Morel, 1994; Vassilev et al.,
1995; Lang et al., 1995). The Cd effect on the photosynthetic system and sugar
accumulation was more expressed in M.9 that in B.396 rootstock plants. In general,
Cd reduced pigment content in plastids.
In contrast to flax callus, which still grew on growth medium supplemented by
100-1000 µM of CdSO4 in vitro (Chakravarty and Srivastava, 1997), our investigated
apple-tree rootstocks were sensitive to Cd contamination as plant growth in vitro
was suppressed or even arrested at such levels of Cd.
Photosynthetic pigment synthesis was inhibited in the leaves of M.9 and B.396
apple-tree rootstocks as a result of Cd presence. Most of authors revealed that
chlorophyll a is more sensitive to Cd impact than chlorophyll b or carotenoids (Vassilev
and Yordanov, 1995; Neelu et al., 2000). According to our results chlorophyll a and
b responded differently to adverse Cd impact. Chlorophylls a to b ratio in apple-tree
rootstock M.9 leaves decreased with increasing CdSO4 concentration. As the
chlorophylls a to b ratio increased in the leaves of B.396 apple-tree rootstocks, it
278
could be assumed that chlorophyll b was more sensitive than chlorophyll a if B.396
plants were grown under 5 and 10 µM amounts of CdSO4. It was shown that
chlorophyll content in Cd treated plants is reduced due to inhibition of its biosynthesis
(Stobart et al., 1985). Such disturbance is determined by the inhibition of
5-aminolaevulinic acid synthesis and by the prevention of formation of photoactive
protochlorophyllide reductase complex. Furthermore, other studies revealed that the
decrease in Mg and Fe content in plant leaves occurred due to Cd treatment (Breckle
and Kahle, 1992; Rubio et al., 1994). Krupa et al. (1995) showed that 50 µM amount
of Cd induced Fe deficiency and decreased chlorophyll content in bean plants by
55%.
Presence of heavy metals alters carbohydrate accumulation and distribution in
plants. As observed by Moya et al. (1993), Cd significantly increased the
carbohydrates content in rice shoots. Our study revealed that Cd significantly increased
the content of fructose and sucrose in leaves of both investigated rootstocks. Thus,
content of fructose increased by a factor of 23-27 and sucrose by a factor of
15-18 in M.9 rootstock leaves as compared to control plants. Meanwhile the content
of fructose and sucrose in the leaves of B.396 rootstocks increased by a factor of
3 and 2-6, respectively. Such phenomenon is likely related to suppressed plant growth
(Greger et al., 1991) or retarded transport of photoassimilates in plants exposed to
heavy metals (Rauser, 1978; Samarakoon and Rauser, 1979). Greger et al. (1991)
proposed that the decrease in growth-intended utilization of carbohydrate caused by
heavy metals is more pronounced than the decrease in CO2 fixation, resulting in an
increased accumulation of carbohydrates.
Conclusions. 1. Even low amounts of Cd in the growth medium suppressed
proliferation and growth of vegetative rootstocks, and inhibited chlorophyll a
biosynthesis in vitro. Chlorophyll b and carotenoids were less sensitive to the Cd
impact.
2. Cd induced the accumulation of fructose and sucrose in the leaves of appletree rootstocks M.9 and B.396. The synthesis of maltose (rootstocks M.9 and B.396),
glucose (rootstock B.396) and µM of Cd were present in the growth medium.
3. The apple-tree rootstock M.9 was more sensitive to the Cd impact than
rootstock B.396. Cd had greater impact on growth, photosynthetic pigment content
and sugar accumulation in the rootstock M.9 leaves than in rootstock B.396 leaves.
Acknowledgement. This work was supported by Lithuanian State Science
and Studies Foundation under project APLIKOM.
Gauta
2006 07 31
Parengta spausdinti
2006 08 03
279
References
1. B a r c e l o J., P o s c h e n r i e d e r C h. Plant water relations as affected
by heavy metal stress: a review // J. Plant Nutrition. 1990. Vol.13. N 1. P.1–37.
2. B a s z y n s k i T., W a j d a L., K r o l M., W o l i n s k a D., K r u p a
Z., T u k e n d o r f A. Photosynthetic activities of cadmium-treated tomato plants //
Physiol. Plantarum. 1980. Vol. 48. P.365–370.
3. B e c e r r i l J., M u n o z - R u e d a A., A p a r i c i o - T e j o P.,
G o n z a l e s - M u r u a C . Changes induced by cadmium and lead in gas exchange
and water relations of clover and Lucerne // Plant Physiol. Biochem 1989. Vol. 27. N 6.
P.913–918.
4. B r e c k l e S., K a h l e H. Effects of toxic heavy metals (Cd, Pb) on growth
and mineral nutrition of beech (Fagus sylvatica L.) // Vegetatio 1992. Vol. 101. P.45–53.
5. C h a k r a v a r t y B., S r i v a s t a v a S. Effects of genotype and explant
during in vitro response to cadmium stress and variation in protein and proline contents
in linseed // Annals of Botany. 1997. Vol. 79. P.487–491.
6. C h u g h L. K., S a w h n e y S. K. Photosynthetic activities of Pisum
sativum seedlings grown in the presece of cadmium // Plant Physiol. Biochem 1999. Vol.
37. P.297–303.
7. C o s t a G., M o r e l J. Water relations, gas exchange and amino acid
content in Cd-treated lettuce // Plant Physiol. Biochem 1994. Vol. 32. N 4. P.561–570.
8. D a v i e s M. S. Effects of toxic metals on root growth and development, in:
Atkinson D. (Ed.), Plant Root Growth: an Ecological Perspective, Special Publication No.
10 of the British Ecological Society, Black-wells Scientific Publications, Oxford, 1991.
P.211–227.
9. G r e g e r M., B e r t e l l G. Effects of Ca2+ and Cd2+ on the carbohydrate
metabolism in sugar beet (Beta vulgaris) // J Exp Bot 1992. Vol. 43. P.167–173.
10. G r e g e r M., B r a m m e r E., L i n d b e r g S., L a r i s o n G.,
I d e s t a m - A l m q u i s t J. Uptake and physiological effects of cadmium in sugar
beet (Beta vulgaris) related to mineral provision // J. Exp. Bot. 1991. Vol. 42. P.729–737.
11. K r u p a Z. Cadmium against higher plant photosynthesis-a variety of effects
and where do they possible come from // Zeitsschrift fuer Naturforschung. 1999. Vol. 54.
P.723–729.
12. K r u p a Z., B a s z y n s k i T. Some aspects of heavy metals toxicity
towards photosynthetic apparatus – direct and indirect effects on light and dark reactions:
a review // Acta Physiol. Plantarum 1995. Vol. 17. N 2. P.177–190.
13. K r u p a Z., S i e d l e c k a A., M a t h i s P. Cd/Fe interaction and its
effects on photosynthetic capacity of primary bean leaves. Proceed. X Intern.
Photosynthesis Congress, Montpellier, France. 1995. P.621–624.
14.L a g r i f f o u l
A.,
Mocquot
B.,
Mench
M.,
V a n g r o n s v e l d J. Cadmium toxicity effects on growth, mineral and chlorophyll
contents, and activities of stress related enzymes in young maize plants (Zea mays L.) //
Plant and Soil. 1998. Vol. 200. N 2. P.241–250.
15. L a n g F., S a r v a r i E., S z i g e t i Z., F o d o r F., C s e h E.
Effects of heavy metals on the photosynthetic apparatus in cucumber. In: Photosynthesis:
from Light to Biosphere, IV, Kluwer Acad. Publishers. 1995. P.533–536.
16. M o y a J. L., R o s R., P i c z o I. Influence of cadmium and nickel on
growth, net photosynthesis and carbohydrate distribution in rice plants // Photosynthesis
Research 1993. Vol. 36. P.75–80.
280
17. M u r a s h i g e T., S k o o g F. A revised medium for rapid growth and
bioassays with tobacco cultures // Physiol Plant. 1962. Vol. 15. P.473–497.
18. N e e l u. K u m a r M., T o m a r M., B h a t n a g a r A. K. Influence
of cadmium on growth and development of Vicia faba Linn // Indian Journal of Experimental
Biology 2000. Vol. 38. N 8. P.819–823.
19. O u z o u n i d o u V., M u s t a k a s M., E l e f t h e r i o u E. P.
Physiological and ultrastructural effects of cadmium on wheat (Triticum aestivum L.)
leaves // Arch. Environ. Contam. Toxicol 1997. Vol. 32. P. 154–160.
20. P a h l s s o n A. M. B. Toxicity of heavy metals (Zn, Cu, Cd, Pb) to vascular
plants // Water Air Soil Poll. 1990. Vol. 47. P.287-319.
21. R a u s e W. E. Early effects of phytotoxic burbens of cadmium, cobalt, nickel
and zinc in white beans // Can J Bot 1978. Vol. 56. P.1744–1749.
22. R u b i o M., E s c r i g I., M a r t i n e z - C o r t i n a C., L o p e z B e n e t F., S a n z A. Cadmium and nickel accumulation in rice plants. Effects on
mineral nutrition and possible interactions of abscisic and gibberellic acids // Plant Growth
Regulation. 1994. Vol. 14. P.151–157.
23. S a m a r a k o o n A. B., R a u s e r W. E. Carbohydrate levels and
photoassimilate export from leaves of Phaseolus vulgaris exposed to excess cobalt, nickel
and zinc // Plant Physiol 1979. Vol. 63. P.1165–1169.
24. S a n d a l i o L. M., D a l u r z o H. C., G o m e z M., R o m e r o P u e r t a s M. C., d e l R i o L. A. Cadmium-induced changes in growth and
oxidative metabolism of pea plant // J. Exp. Bot 2001. Vol. 52. P.2115–2126.
25. S a n i t a d i T o p i L., G a b b r i e l l i R. Response to cadmium in
higher plants // Environ. Exp. Bot. 1999. Vol. 41. P.105-130.
26. S a r v a r i E., F o d o r F., C s e h E., V a r g a A., Z a r a y G.,
Z o l l a L. Relationship between changes in ion content of leaves and chlorophyll protein composition in cucumber under Cd and Pb stress // Biosciences. 1999. Vol. 54. N 9/
10. P.740–745.
27. S i e d l e c k a A. Some aspects of interactions between heavy metals and
plant mineral nutrients // Acta Soc. Bot. Pol. 1995. Vol. 64. P.265–272.
28. S o m a s h e k a r a i a h B. V., P a d m a j a K., P r a s a d A. R. K.
Phytotoxicity of cadmium ions on germination seedlings of mug bean (Phaseolus vulgaris)
- involvement of lipid peroxides in chlorophyll degradation // Physiol. Plant. 1992. Vol. 85.
P.85–89.
29. S t o b a r t A., G r i f f i t h s W., A m e e n - B u k h a r i I.,
S h e r w o o d R. The effect of Cd2+ on the biosynthesis of chlorophyll in leaves of
barley // Physiol. Plantarum. 1985. Vol. 63. P.293–298.
30. S t o h s S. J., B a g c h i D., H a s s o u n E., B a g c h i M.
Oxidative mechanisms in the toxicity of chromium and cadmium ions // J. Environ. Pathol.
Toxicol. Oncol. 2000. Vol. 19. P.201-213.
31. S t r o i s k i A., K o z l o w s k a M. Cadmium-induced oxidative stress in
potato tuber // Acta Soc. Bot. Pol. 1997. Vol. 66. P.189–195.
32. V a n A s s c h e F., C l i j s t e r s H. Effects of metalo n enzime activity in
plants // Plant Cell Environ. 1990. Vol. 13. P.195–206.
33. V a s s i l e v A., Y o r d a n o v I., C h a k a l o v a E., K e r i n V.
Effect of cadmium stress on growth and photosynthesis of young barley (H. vulgare L.)
plants. Structural and functional changes in photosynthetic apparatus // Bulg. J. Plant
Physiol. 1995. Vol. 21. N 4. P.12–21.
34. W e t t s t e i n D. Chlorophyll Letale und der submikroskopishe Formweschsel
der Plastiden. Experimental cell research. 1957. Vol. 12. P.427.
281
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
273–282.
OBELØ POSKIEPIØ M.9 IR B.396 ATSPARUMAS KADMIO JONØ
POVEIKIUI IN VITRO
J. Sakalauskaitë, G. Stanienë, V. Stanys, P. Duchovskis, G. Samuolienë,
K. Baranauskis, A. Urbonavièiûtë, V. Revin, A. Lukatkin
Santrauka
Tyrimo tikslas – ávertinti kadmio (Cd) jonø poveiká obelø poskiepiø M.9 ir B.396
regeneracijai, fotosintetinio aparato kûrimui ir angliavandeniø sintezei in vitro augimo
terpëje. Cd jonai labiau stabdë M.9 poskiepio mikroûgliø augimà nei B.396 poskiepio. Net
ir nedidelis CdSO4 kiekis maitinamojoje terpëje chlorofilo a kieká lapuose sumaþino ið
esmës. Chlorofilo b ir karotinoidø kiekis mikroûgliø lapuose priklausë nuo Cd koncentracijos
auginimo terpëje ir poskiepio genetinës prigimties. Cd skatino fruktozës ir sacharozës
kaupimàsi abiejø poskiepiø lapuose. Kai terpëje CdSO4 koncentracija buvo 10 µM, M.9
poskiepio mikroûgliø lapuose pradëjo kauptis maltozë, kai 5 ir 10 µM – B.396 poskiepio
lapuose kaupësi gliukozë, galaktozë ir maltozë. Poskiepiai M.9 ir B.396 skirtingai reagavo á
Cd poveiká: Cd turëjo didesnës átakos mikroûgliø augimui, pigmentø kiekiui ir cukrø kitimams
M.9 poskiepio lapuose nei B.396 poskiepio.
Reikðminiai þodþiai: in vitro, kadmis (Cd), mono- ir disacharidai, pigmentai, M.9 ir
B.396 poskiepiai.
282
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 283–291.
BIOMASS PRODUCTION, DRY WEIGHT PARTITIONING
AND LEAF AREA OF APPLE ROOTSTOCKS UNDER
DROUGHT STRESS
Jurga SAKALAUSKAITË, Darius KVIKLYS,
Juozas LANAUSKAS, Pavelas DUCHOVSKIS
Lithuanian Institute of Horticulture, Kauno str. 30, LT-54333 Babtai,
Kaunas distr., Lithuania. E-mail: [email protected]
The influence of water deficiency on apple (Malus domestica Borkh.) rootstocks
was investigated at the Lithuanian Institute of Horticulture in 2005. Trial was conducted
with 10 rootstocks: Antonowka seedling, MM.106, M.26, B.118, M.9, P 60, P 59, P 2, B.396,
and P 22 under three soil moisture regimes. After an initial period of growth under wellwatered conditions the amount of irrigation was gradually reduced in order to simulate
natural drying in the soil. Biometric indices – assimilation area, fresh and dry weight of
leaves, shoots and roots were measured after 5 weeks of the experiment. Moderate drought
stress suppressed the accumulation of fresh and dry weight in all investigated rootstocks,
except seedling rootstock, where accumulation of fresh and dry weight was induced.
Moderate drought also induced the growth of leaves of seedling rootstock, MM 106, and
P 59. Severe drought negatively affected the accumulation of fresh and dry weight of all
apple rootstocks. Reduction to 50% was determined in comparison to control plants.
Severe drought induced premature leaves senescence and shedding. Water stress altered
partitioning of dry mass, especially under severe drought stress. Higher allocation of total
plant dry weight into shoots and roots instead of leaves was observed under severe
drought stress. According to fresh and dry weight accumulation, P 22, B.118, P 60 and
seedling rootstocks were the most drought resistant. M.26, M.9, P 2 and B.396 rootstocks
were the most sensitive to water deficiency. According to leaf area changes, M.26, P 2 and
B.396 rootstocks were the most drought sensitive. Moderate drought stress did not affect
leaf area of seedling, MM.106, B.118, M.9, P 59, and P 22 rootstocks.
Key words: Malus x domestica, fresh and dry weight, rootstock, water stress.
Introduction. Different rootstock genotypes have different adaptability to various
climatic and soil conditions. More dwarfing rootstocks have shallower root system
and usually in commercial growing they are used to be irrigated. Nevertheless,
rootstock performance under water deficiency is different. Though, there is only
limited information on the drought tolerance of apple rootstocks (Wertheim, 1998),
some researches established that P 22 rootstock seems to be more suitable to soils
with a low content of water than P 16 (Klamkowski, Treder, 2002). There are reports
that M.111 and M.26 rootstocks show good drought tolerance (Atkinson et al., 2000;
283
Ferree, Carlson, 1987). Drought tolerance of M.9 rootstock is also highly evaluated
(Fernandez et al., 1997; Klamkowski, Treder, 2002). There was established that
P 60 rootstock under Lithuanian climatic conditions does not need irrigation
(Duchovskis et al., 2000; Kviklys, Petronis, 2000).
Periods of soil water deficit of varying length and severity commonly occur
during the growing season. Drought is one of the most severe environmental stresses
and affects almost all the plant functions (Kazuko Yamaguchi-Shinozaki et al., 2002).
Since water stress can reduce plant growth, soil water availability may thus be an
important production determinant (Schulze, 1986). Water deficit can affect plants in
different ways. In the frame of “physiological window” mild drought induces in
plants regulation of water loss and uptake, allowing maintenance of their leaf relative
water content within the limits where photosynthetic capacity and quantum yield
show little or no change. The most severe form of water deficit is desiccation –
when most of the protoplasmic water is lost and only a very small amount of tightly
bound water remains in the cell (Yordanov, 2003).
Productivity of crops under drought stress condition is strongly related to the
processes of dry matter partitioning in the plant and the spatial and temporal root
distribution (Kage et al., 2004). Water stress, however, can affect the growth of
each plant organ differently, and the pattern of dry mass accumulation within the
plant may thus be altered (Atkinson et al., 1998). The development of crop leaf area
is controlled by the amount of assimilates allocated to the leaves and determines
radiation interception and therefore transpiration and assimilate production (Jones,
1992; Campbell, Norman, 1998). An optimal partitioning of dry matter between root
and shoot, and the further separation of aboveground dry matter between the vegetative
and generative organs has crucial importance for crop yield under drought stress
conditions. Drought stress mostly reduces leaf growth and increased dry matter
allocation into the root fraction, leading to a declining shoot/root-ratio (Wilson, 1988).
The yield effect of this adaptation process, however, depends strongly upon time
and extends of drought stress (Campbell, Turner, 1990).
The aim of the present study was to investigate biometric changes of apple
rootstocks induced by drought stress grown under natural weather condition, but
with controlled water regime.
Materials and methods. 1-year-old apple rootstocks (‘Antonowka’ seedling,
MM.106, M.26, B.118, M.9, P60, P59, P 2, B.396, P 22) were planted in early
vegetative growth phase in plastic pots. 10 different rootstocks were potted in each
pot. Potted trees were grown outdoors under natural weather conditions and watered
equally until midsummer. Potted rootstocks were transferred to plastic greenhouse
when drought stress treatment was initiated. Three soil moisture regimes were created:
20–30 kPa (control), 40–50 kPa and >70 kPa. Rootstocks were grown under such
conditions for 5 weeks. Moisture content in the soil was measured by tensiometer.
Biometric measurements were done at the end of experiment. Whole plants of
each rootstock were harvested, and then the individual plant samples were divided
into stems, leaves and roots. Roots were washed and cleaned from organic debris.
Plant tissues were oven-dried at 105°C for 24 h to determine dry weight. Leaf area
meter WinDias (U.K) was used for assimilation area measurements. Experiment was
carried out in four replications.
284
Statistical analysis was performed using one-way and two-way ANOVA. Means
were separated by Fisher’s Least Significant Difference (P≤0.05 and P≤0.01) and
Duncan’s Multiple Range t-test procedure (P≤0.05).
Results. Drought stress significantly decreased the accumulation of total fresh
and dry weight on the average of all rootstocks (Table 1). Significant differences
were recorded for all watering regimes.
T a b l e 1. The total fresh and dry weight of apple rootstocks under
different drought treatment, g (the average of ten
rootstocks)
1
l e n t e l ë.
Bendra poskiepiø þalia ir sausa masë, esant skirtingiems drëgmës
reþimams, g (deðimties poskiepiø vidurkis)
Fresh weight / Žalia masë
Dry weight / Sausa masë
20–30 (control / kontrolë)
40–50
>70
90.97
64.54
51.56
41.92
30.43
25.43
LSD05/R05
LSD01/R01
5.56
7.37
2.67
3.53
Drought treatment /Sausros režimas, kPa
According to accumulation of fresh and dry weight apple rootstocks responded
differently to drought stress (Table 2, 3). The accumulation of fresh weight was
inhibited in all rootstocks exposed to moderate water stress, except seedlings that
accumulated about 30% more of fresh weight as compared to control plants
(20–30 kPa). At the same regime fresh weight accumulation in rootstocks M.26,
M.9 and P 2 was suppressed by 50%.
T a b l e 2. Total fresh weight of apple rootstocks exposed to different
water stress, g
2
l e n t e l ë.
Obelø poskiepiø bendra þalia masë, esant skirtingiems drëgmës
reþimams, g
Rootstock / Poskiepiai
Seedling / Sëklinis
MM.106
M.26
B.118
M.9
P 60
P 59
P2
B.396
P 22
Drought treatment / Sausros režimas, kPa
20–30 (control / kontrolë)
40–50
>70
62.51 a
93.32 a
74.05 a
87.08 a
130.57 a
98.32 a
97.50 a
95.12 a
92.11 a
79.17 a
79.54 a
67.81 ab
42.75 b
71.94 ab
70.34 b
73.43 a
88.08 a
45.11 b
55.51 b
50.90 a
52.64 a
49.28 b
41.50 b
40.46 b
56.18 b
62.20 a
55.06 b
44.44 b
56.18 b
57.75 a
Means in the line marked with the same letter do not differ significantly at P≤0.05
Ta paèia raide paþymëtos reikðmës eilutëje ið esmës nesiskiria (P≤0,05).
285
Under severe drought (>70 kPa), total fresh weight accumulation of rootstocks
MM.106, M.26, M.9, P 59, P 2 and B.396 significantly decreased as compared to
control plants. There were no significant differences between all watering regimes
in total fresh weight of P 22, seedling, and P 60 rootstocks.
Similar tendencies of dry weight variation were determined too. At the end of
experiment, the dry weight accumulation of stressed apple rootstocks tended to
decrease with the intensity of drought stress (Table 3). Under the severe stress at the
end of the experiment, total dry weight accumulation in rootstocks dropped to 50%.
At the end of the experiment, total dry weight of M.9, P 2, M.26 and B.396
rootstocks under moderate and severe drought significantly decreased. The total dry
weight of P 59 and MM.106 rootstock significantly decreased only in severe drought.
There were no significant differences between all watering regimes in the total dry
weight of P 22, seedling, B.118 and P 60 rootstocks.
T a b l e 3. Total dry weight of apple rootstocks exposed to different
water stress, g
3
l e n t e l ë.
Rootstock / Poskiepiai
Seedling / Sëklinis
MM.106
M.26
B.118
M.9
P 60
P 59
P2
B.396
P 22
Obelø poskiepiø bendra sausa masë, esant skirtingiems drëgmës
reþimams, g
Drought treatment / Sausros režimas, kPa
20–30 (control / kontrolë)
40–50
>70
29.08a
43.50a
34.59a
40.70a
61.16a
45.55a
41.29a
44.24a
42.32a
36.79a
37.92a
30.59a
20.61a
34.09a
35.06b
33.63a
38.30a
21.32b
27.87b
24.94a
26.74a
24.53a
21.23a
21.12a
29.54b
29.02a
24.46b
21.62b
25.94b
30.08a
Means in the line marked with the same letter do not differ significantly at P≤0.05
Ta paèia raide paþymëtos reikðmës eilutëje ið esmës nesiskiria (P≤0,05).
Water stress altered the partitioning of rootstock dry mass (Fig. 1). Partitioning
of total plant dry weight to leaves of seedling, MM.106 and M.9 rootstocks were
greater under moderate water stress. The accumulation of total dry weight to shoots
was more induced in rootstocks P 59 and P 2. Partitioning of total plant dry weight
to roots of B.396 and P 60 rootstocks was greater under moderate water stress.
While partitioning of total dry mass of rootstocks M.26 and B.118 was not altered
under moderate water stress. Higher allocation of total plant dry weight to shoots
and roots instead to leaves was considerably expressed in all rootstocks under severe
drought stress.
286
F i g. 1. Dry weight partitioning into various organs of apple rootstocks exposed to
different water stress, %
1
p a v. Sausos masës pasiskirstymas ávairiose obels poskiepiø dalyse, %
287
The moderate drought stress stimulated growth of leaves of seedling, MM.106,
M.9, P 59 and P 22 rootstocks as compared to control plants (Fig. 2). Other rootstocks
B.118, P 60, M.26, B.396 and P 2 shed accordingly 10%, 20%, 40%, 45% and 50%
of the leaves under moderate water stress. The severe drought induced premature
leaves senescence and shedding of all rootstocks. It was determined 30-80% leave
loss of various rootstocks exposed to severe drought. According to leave area changes
the most sensitive rootstocks to drought stress were M.26, B.396 and P 2.
F i g. 2. Changes in leaf area of apple rootstocks under moderate (40-50 kPa) and
severe (>70 kPa) drought stress. The values are expressed as a percentage variation
of total leave area in (20-30 kPa) control treatment, %
2 p a v. Poskiepiø lapø ploto pokytis, esant skirtingiems drëgmës reþimams.
Vertës iðreikðtos kaip procentinis pokytis poskiepiø, augusiø normaliomis drëgmës
sàlygomis, %
Discussion. The drought treatment resulted in large decrease in total fresh
weight of all apple rootstocks. Rootstock fresh weight declined with increasing soil
drying for the majority of rootstocks tested. Even moderate drought stress inhibited
the accumulation of fresh weight, except seedling rootstock. The total fresh weight
decreased significantly for semi-dwarf M.26 and dwarf M.9, P 2 and B.396 rootstocks,
though in some experiments higher drought resistance of M.26 was recorded (Atkinson
et al., 1998). Consequently, drought-induced decreases of rootstocks fresh weight
were accompanied by reduction in total dry weight. Total dry weight of all rootstocks
declined with increasing soil drying. Tested rootstocks can be grouped into two
separate groups according to decreased total dry weight at the end of experiment:
rootstocks MM.106, M.26, B.118, M.9, P 60, P 59, P 2 and B.396, which dry weight
declined by 40-50%, and another group – seedling rootstock and P 22, which dry
weight declined by 10-20 %, compared to control plants. Higher drought resistance
of P 22 rootstock was noted in Polish trials, though it was less resistant as M.9
(Klamkowski, Treder, 2002). Our study results showed opposite tendency – super
dwarfing P 22 was more resistant to water deficiency as dwarfing and semi dwarfing
rootstocks.
Soil moisture changes not only affect the plant biomass dry weight, but also the
distribution of assimilates to roots and shoots (Amdt et al., 2001; Ranney et al.,
1990). Under the influence of hormones synthesized in the leaves and roots in response
to drought, changes occur in the allocation of assimilates, the ratio of shoot to root
288
growth is altered (Larcher, 1995). In our investigation drought also affected dry
matter partitioning, resulting in more dry matter partitioning to root or shoot systems.
Even moderate water stress induces intensive dry weight accumulation in shoots or
roots of rootstocks P 59, P 2 and B.396. Usually above ground plant growth decreased
by changes in biomass partitioning that favoured root system development. Thus
plants can exploit the limiting water resource in a more efficient way by increasing
the proportion of water absorbing root biomass relatively to the water-loosing leaf
biomass (Duan et al., 2005; Li, 1999; Yanbao Lei et al., 2006; Zhang et al., 2004).
Such tendencies were noted in our trial too.
Under severe drought stress apple rootstocks had lower values of leaf area than
the well-watered controls, indicating that drought induced premature leave senescence
and shedding. Under moderate water stress differences in the growth of leaves were
recorded between various rootstocks: seedling rootstock increased its leaf area by
50%, MM.106 – 10%, M.9 – 5%, P 59 – 25%, P 22 – 6%, while other rootstocks
M.26, B.118, P 60, P 2, B.396 shed leaves to some extent. Dwarf rootstocks P 2 and
B.396 decreased their leaf area to a great extent under moderate water stress. Among
the 10 used apple rootstocks, leaf area of super dwarfing P 22 and dwarfing P 60
were least affected by drought stress. Good performance of the latter rootstock in
not irrigated orchards was noted in our previous trials (Duchovskis et al,. 2000;
Kviklys, Petronis, 2000). This could be ascribed to their low stomatal conductance,
which enabled the plants to control water status restrictively when water uptake by
the root was curtailed as the soil dried. According Atkinson (2002) for the range of
rootstocks examined, stomatal conductance was generally greater for the more growth
invigorating rootstocks than for the restricting.
There was no relationship between rootstock drought hardiness and ability of
the rootstock to control scion vigour. Semi dwarf M.26, dwarf M.9, P 2 and B.396
rootstocks were more sensitive to water deficiency as super dwarf P 22 and P 59
rootstocks. Such findings are confirmed by other trials too (Atkinson, 2000).
Our results confirm the existence of genetic differences in the fresh and dry
matter accumulation, dry matter allocation and leave area as affected by water stress.
These variations in drought responses may be used as criteria for rootstock selection
and tree improvement.
Conclusions. Rootstock fresh and dry weight declined with increasing soil
drying. According to fresh and dry weight accumulation, M.26, M.9, P 2 and B.396
rootstocks are the most drought sensitive. MM.106 and P 59 rootstocks reacted
negatively only in severe drought conditions. P 22, B.118, P 60 and seedling rootstock
were most resistance to water deficiency.
According to leaf area changes, M.26, P 2 and B.396 rootstocks were the most
drought sensitive. Moderate drought stress did not affect leaf area of seedling,
MM.106, B.118, M.9, P 59, and P 22 rootstocks. Thought severe drought conditions
decreased leaf area of all rootstocks, P 22 and P 60 rootstocks were less affected.
Higher allocation of total plant dry weight into shoots and roots instead of leaves
was observed under severe drought stress.
Acknowledgement. This work was supported by Lithuanian State Science
and Studies Foundation under project FIBISTRESS.
289
Gauta
2006 07 11
Parengta spausdinti
2006 08 02
References
1. A m d t S. K., C l i f f o r d S. C., W a n e k W., J o n e s H. G., P o p p
M. Physiological and morphological adaptations of the fruit tree Ziziphus rotundifolia in
response to progressive drought stress // Tree Physiol. 2001. Vol. 21. P.705–715.
2. A t k i n s o n C. J. Using rootstocks to optimize fruit tree water use // Compact
fruit tree. 2002. Vol. 35 (1). P. 12–18.
3. A t k i n s o n C. J., P o l i c a r p o M., W e b s t e r A. D.,
K i n g s w e l l G. Drought tolerance of clonal Malus determined from measurements of
stomatal conductance and leaf water potential // Tree Physiology. 2000. Vol. 20. P.557–563.
4. A t k i n s o n C. J., P o l i c a r p o M., W e b s t e r A. D., K u d e n
A. M. Drought tolerance of apple rootstocks: Production and partitioning of dry matter
// Plant and Soil. 1998. Vol. 206 (2), P. 223–235.
5. C a m p b e l l G. S., N o r m a n J. M. Environmental Biophysics. SpringerVerlag, New York Berlin Heidelberg. 1998.
6. C a m p b e l l G. S., T u r n e r N. C. Plant–soil–water relationships. In:
Solomon, K.H. (ed.), Management of farm irrigation systems, American Society of
Agricultural Engineers, St. Joseph, MI. 1990. P.13–29.
7. D u a n B., L u Y., Y i n C., J u n t t i l a O., L i C. Physiological
responses to drought and shade in two contrasting Picea asperata populations // Physiol
Plant. 2005. Vol. 124. P.476–484.
8. D u c h o v s k i s P., K v i k l y s D., K a w e c k i Z., P e t r o n i s P.,
K v i k l i e n ë N. Impact of rootstock and irrigation on apple bud differentiation and
flowering initiation // Sodininkystë ir darþininkystë. 2000. Vol. 19. N (3)-1. P.352—358.
9. F e r n a n d e z R. T., P e r r y R. L., F l o r e J. A. Drought response of
young apple trees on three rootstocks: growth and development. J.Amer. Soc. Hort. Sci.
1997. Vol.122:14–19.
10. F e r r e e D. C., C a r l s o n R. F. Apple rootstocks. In: R.C. Rom and R.F.
Carlson (eds.) Rootstocks for Fruit Crops. 1987. Wiley-Interscience Publication, John
Wiley and Sons, New York. P. 107–143.
11. J o n e s G. H. Plants and Microclimate: A Quantitative Approach to
Environmental Plant Physiology. University Press, Cambridge. 1992.
12. K a g e H., K o c h l e r M., S t ü t z e l H. Root growth and dry matter
partitioning of cauliflower under drought stress conditions: measurement and simulation
// Europ. J. Agronomy. 2004. Vol. 20. P. 379–394.
13. K a z u k o Y a m a g u c h i - S h i n o z a k i, M i e K a s u g a, Q i a n g
L i u, K a z u o N a k a s h i m a, Y o h S a k u m a, H i r o s h i A b e.
Population differences in water-use efficiency of Eucalyptus microtheca seedlings under
different watering regimes // Physiol Plant. 2002. Vol.108. P.134–139.
14. K l a m k o w s k i K., T r e d e r W. Influence of a rootstock on transpiration
rate and changes in diameter of an apple tree leader growing under different soil water
regimes // J.Fruit Ornam. Plant Research. 2002. Vol. 10. P.31–39.
15. K v i k l y s D., P e t r o n i s P. Þemaûgiø obelø poskiepiø átaka vaismedþiø
augumui jauname sode // Sodininkystë ir darþininkystë. 2000. T. 19(1). P.15– 22.
16. L a r c h e r W. Physiological plant ecology. Third edition, Springer. 1995. P. 504.
17. L i C. Carbon isotope composition, water-use efficiency and biomass
productivity of Eucalyptus microtheca populations under different water supplies // Plant
290
Soil. 1999. Vol. 214. P.165–171.
18. R a n n e y T. G., W h i l o w T. H. B a s s u k N. L. Response of five
temperate deciduous tree species to water stress // Tree Physiol. 1990. Vol. 6. P.439– 448.
19. S c h u l z e E. D. Whole-plant responses to drought // Australian Journal of
Plant Physiology. 1986. Vol. 13. P.127–141.
20. W i l s o n J. B. A review of evidence on the control of shoot:root ratio, in
relation to models // Annals of Botany. 1988. Vol. 61. P. 433–449.
21. Y a n b a o L e i, C h u n y i n g Y i n a, C h u n y a n g L i. Differences
in some morphological, physiological, and biochemical responses to drought stress in
two contrasting populations of Populus przewalskii // Physiologia Plantarum. 2006. Vol.
127. P.182–191.
22. Y o r d a n o v I., V e l i k o v a V., T s o n e v T. Plant responses to
drought and stress tolerance // Bulg. J. Plant Physiol., special issue. 2003. P. 187–206.
23. Z h a n g X, Z a n g R, L i C. Population differences in physiological
and morphological adaptations of Populus davidiana seedlings in response to progressive
drought stress // Plant Sci. 2004. Vol. 166. P.791–797.
24. W e r t h e i m S. J. Rootstock Guide. Apple, Pear, Cherry, European Plum.
Fruit Research Station. The Netherlands. 1998. P. 144.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
283–291.
SAUSROS SUKELTO STRESO ÁTAKA OBELØ POSKIEPIØ BIOMASEI,
SAUSOS MASËS PASISKIRSTYMUI IR LAPØ PLOTUI
J. Sakalauskaitë, D. Kviklys, J. Lanauskas, P. Duchovskis
Santrauka
Tyrimø tikslas – nustatyti vandens trûkumo átakà ávairiems obelø poskiepiams.
Bandymai atlikti Lietuvos sodininkystës ir darþininkystës instituto Augalø fiziologijos
laboratorijos vegetacinëje aikðtelëje. Tirti sëkliniai, MM.106, M.26, B.118, M.9, P 60, P 59,
P 2, B.396 ir P 22 poskiepiai. Tyrimo metu palaikyti skirtingi dirvos drëgmës reþimai:
20–30 kPa (kontrolë), 40–50 kPa ir >70 kPa. Tyrimo pabaigoje nustatyta, kiek sukaupta
þalios ir sausos masës, ir iðmatuotas lapø plotas. Vidutinis sausros sukeltas stresas
(40–50 kPa) slopino þalios ir sausos masës kaupimàsi visuose poskiepiuose, iðskyrus
sëkliná; jame þalios ir sausos masës kaupimasis buvo skatinamas (sukaupë iki 30% daugiau
nei kontroliniai augalai). Vidutinis sausros sukeltas stresas taip pat paskatino sëklinio
poskiepio, MM.106, M.9, P 59 ir P 22 poskiepiø lapø augimà, o kiti poskiepiai pradëjo mesti
lapus. Stiprus sausros sukeltas stresas neigiamai paveikë ir þalios, ir sausos masës kaupimàsi
visuose poskiepiuose. Nustatyta, kad palyginti su kontroliniais poskiepiais, þalios ir
sausos masës sumaþëjo iki 50%. Sausrai sukëlus didelá stresà, visø poskiepiø lapai vyto ir
krito per anksti. Sausros sukeltas stresas pakeitë ir sausøjø medþiagø pasiskirstymà ávairiose
poskiepiø dalyse. Intensyvus sausros sukeltas stresas skatino daugiau sausøjø medþiagø
kauptis ðaknyse ar ûgliuose nei lapuose. Pagal þalios ir sausos masës kaupimàsi nustatyta,
kad jautriausi sausrai yra M.26, M.9, P 2 ir B.396 poskiepiai, atspariausi – P 22, B.118, P 60
ir sëklinis poskiepiai. Pagal lapø ploto pokytá jautriausi sausrai yra M.26, P 2 ir B.396
poskiepiai. Vidutinis sausros sukeltas stresas neturëjo átakos sëklinio, MM.106, B.118,
M.9, P 59 ir P 22 poskiepiø lapø dydþiui.
Reikðminiai þodþiai: Malus x domestica, poskiepis, sausa ir þalia masë, sausros
sukeltas stresas.
291
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 292–295.
THE INFLUENCE OF DIFFERENT ROOTSTOCKS ON
THE GROWTH, YIELD AND FRUIT QUALITY OF PLUM
TREE CV. ‘DÀBROWICE PRUNE’ PLANTED IN
EXHAUSTED SOIL
S. Zygmunt GRZYB, Miroslaw SITAREK
Research Institute of Pomology and Floriculture, Pomologiczna 18, 96–100
Skierniewice, Poland. E-mail: [email protected]
The growth and yield of plum tree cv. ‘Dàbrowice Prune’ grafted on two seedling
rootstocks (P. cerasifera var. divaricata Borkh. and ‘Wangenheim Prune’) as well as on
four clonal rootstocks (Jaspi, GF 655/2, Ishtara and St. Julien A) were investigated in the
young orchard. Trees were planted at a spacing of 4.25 x 2.5 m in the soil used for fruit tree
crops for at least 50 years. Cherry, apple and plum trees were cultivated previously on this
field. Analysis of tree growth and cumulative yield revealed that plum trees on seedlings
Wangenheim Prune grew less vigorously and had lower cumulative yield than the control
ones grafted on P. divaricata. The growth and yield reductions in case of trees on seedlings
‘Wangenheim Prune’ were untypical in this experiment as a comparison to trees on the
same rootstocks located in other places. Replant problems of plum trees grafted on four
other investigated rootstocks were not observed in such big scale like on seedlings of
‘Wangenheim Prune’
Key words: plum, Prunus domestica L., rootstock, cultivar, growth, yield, fruit weight,
replant problems.
Introduction. Plum trees in Poland are grown mainly on Prunus cerasifera var.
divaricata Led. (Grzyb and Rozpara, 1998). This rootstock is classified as vigorous
(Grzyb et al., 1984; Ystaas and Froynes, 1993) and is unsuitable for intensive plum
orchards. In this respect trees grafted on seedlings of Wangenheim Prune are more
suitable for this type of orchards. According to the results obtained by several authors
(Grzyb and Krzewiñska, 1992; Grzyb et al., 1998a; Rozpara and Grzyb, 1994; Rozpara
and Grzyb, 1998; Sitarek and Grzyb, 2002; Sitarek et al., 2004), this rootstock
reduced significantly the growth of plum trees and improved their productivity in
comparison to P. divaricata seedlings. However, some plum cultivars on seedlings
of ‘Wangenheim Prune’ had the tendency to decrease mean fruit weight, particularly
on sandy soils (Grzyb et al., 1998 b). Therefore, the search was undertaken to find
out new dwarf or semi dwarf rootstocks for plums well adapted to Polish growing
conditions. For experiments, for the evaluation of new rootstocks there were included
292
in West European countries well know vegetative propagated rootstocks commonly
used in commercial orchards. Among them there are types of French, German and
English selection.
Materials and methods. In field experiment plum trees of cv. ‘Dàbrowice
Prune’ grafted on seedlings of ‘Wangenheim Prune’ and four vegetative propagated
rootstocks (Jaspi, GF 655/2, Ishtara and St. Julien A) were compared with trees on
P. divaricata seedlings. In the spring of 2000 one-year-old trees were planted at the
“Pomological Orchard” in Skierniewice. Trees were planted in the soil used before
for fruit tree crops for at least 50 years. Cherry, apple and plum trees were cultivated
previously on this field. The trees were planted in light loamy soil at a spacing of
4.25 x 2.5 m. Experiment was established in the random blocks design with four
replications, with three trees per plot. The total number of 12 trees in each rootstock/
cultivar combination was investigated. Plum orchard was irrigated. During the first
year after planting the soil was kept free from weeds by mechanical cultivation. In
the following years soil management included frequent grass mowing in the alleyways
in conjunction with the maintenance of less than 1-m wide herbicide strips along the
tree rows. Herbicides and fertilizers were applied according to the standard
recommendation for plum commercial orchards. Trees were trained as free spindles
with a central leader. The following traits were evaluated: tree vigor, yield, fruit
weight and the soluble solids. The results of obtained data were statistically analyzed
and Duncan’s multiple range t-tests at the probability level of 5% was used to separate
statistically different means.
Results. The results revealed that only seedlings Wangenheim Prune reduced
significantly the growth of plum trees ‘Dàbrowice Prune’ in comparison to
P. divaricata (Table). The decrease of tree grow of this cultivar was influenced also
by GF 655/2 and St.Julien A rootstocks. Trees grafted on Ishtara grew very vigorously.
Cumulative yield of ‘Dàbrowice Prune’ was not affected by the type of
rootstocks, except of ‘Wangenheim Prune’ seedlings. The trees grafted on seedlings
of Wangenheim Prune had significantly lower yield than on the other tested rootstocks
grown in the same conditions.
Yield efficiency was similar for all these trees. Differences among rootstocks
were not significant. Plum trees ‘Dàbrowice Prune’ grafted on Jaspi and Ishtara
produced larger fruits than trees grafted on P. cerasifera var. divaricata. The highest
content of soluble solids was established in the fruits collected from the trees grafted
on St. Julien A.
Discussion. Seedlings of ‘Wangenheim Prune’ used as a rootstock in this trial
significantly reduced the growth of fruit tree cv. ‘Dàbrowice Prune’. This corresponds
to results obtained by other authors (Grzyb et al., 1998b; Grzyb and Sitarek, 2004;
Sitarek et al., 2004). However, the scale of growth reduction intensity was relatively
too big and not corresponded to data obtained with this rootstock located in other
places (Grzyb and Rozpara, 1998; Rozpara and Grzyb, 1998; Sitarek et al., 2001;
Sitarek et al., 2004). It seemed to be as consecutive effect of exhausted soil, because
cherry, apple and plum trees were cultivated previously on this field (Pacholak, 2003a;
Pacholak, 2003 b; Grzyb and Sitarek, 2004). Such problem in this scale was not
observed with trees grafted on other investigated rootstocks. In this location plum
293
trees on Ishtara rootstock grew as intensively as trees grafted on seedlings
P. cerasifera. In comparison to control trees other investigated rootstocks (except
of ‘Wangenheim Prune’ seedlings) only slightly limited the growth intensity of
‘Dàbrowice Prune’.
T a b l e. Growth and yield of plum trees cv. ‘Dàbrowice Prune’ grafted
on different rootstocks and cultivated in replant
conditions. Experimental Orchard at Skierniewice, Central
Poland, 2000–2005
L e n t e l ë. Pakartotinai auginamø slyvø, áskiepytø á skirtingus poskiepius,
augimas ir derlius. Bandymø sodas Skierniewice, centrinëje
Lenkijoje, 2000–2005 m.
Trunk cross
sectional area
(TCSA) in 2005
Kamieno skerspjûvio
plotas (KSP) 2005 m.
Rootstock
Poskiepis
cm2
P.divaricata
‘Wangenheim
Prune’
Jaspi
GF 655/2
Ishtara
St. Julien A
%
Cumulative
yield
2002–2005
Suminis derlius
2002–2005 m.
kg tree-1
kg vaism.
-1
Yield efficacy Mean fruit
weight
2002–2005
Produktyvumas
2002–2005 m.
kg cm-2 of
TCSA
Soluble
solids
Vidutinë
vaisiaus
masë
Tirpios
sausosios
medžiagos
g
%
kg cm-2 KSP
75.5 c*
100.0
29.0 b
0.39 a
32.7 a
18.1 ab
41.8 a
55.4
16.8 a
0.42 a
33.9 a
19.2 ab
67.7 bc
60.9 b
78.0 c
59.2 b
89.7
80.7
103.3
78.4
31.9 b
23.4 ab
30.0 b
26.5 b
0.49 a
0.38 a
0.39 a
0.46 a
37.0 b
35.3 ab
36.4 b
35.2 ab
17.7 a
18.4 ab
18.5 ab
19.8 b
* Means followed by the same letter in the columns are not significantly different at
P = 0.05 according to Duncan’s test / Ta paèia raide paþymëtos reikðmës skiltyse pagal Dunkano
kriterijø (p = 0,05) ið esmës nesiskiria.
Conclusions. The most vigorous growth of replanted plum trees cv. ‘Dàbrowice
Prune’ was on rootstock Ishtara and Prunus divaricata seedlings. Trees on Jaspi and
Ishtara produced the largest fruits. Cummulative yield was simmilar on all tested
rootstocks except seedlings of ‘Wangenheim Prune’.
In exhausted soil the most limited growth and productivity of plum trees was
on seedlings of ‘Wangenheim Prune’.
Gauta
2006 05 23
Parengta spausdinti
2006 07 17
References
1. G r z y b Z. S., J a c k i e w i c z A., C z y n c z y k A. Results of the 18year evaluation of rootstocks for Italia Prune cultivar. Fruit Sci. Rep. 1984. 11(3). P. 99–104.
294
2. G r z y b Z. S., R o z p a r a E. Plum production in Poland. Acta Hort. 1998.
478. P. 19–24.
3. G r z y b Z. S., S i t a r e k M., K o l o d z i e j c z a k P. Growth and
yield of Tree plum cultivar grafted on four rootstocks in Piedmont area. Acta Hort. 1998a.
478. P. 87–90.
4. G r z y b Z. S., S i t a r e k M., K o z i n s k i B. Effect of different
rootstocks on growth, yield and fruit quality of four plum cultivars ( in central Poland).
Acta Hort. 1998 b. 478. P. 239–242.
5. G r z y b Z. S., S i t a r e k K. Growth and yield of two plum cultivar grafted
on Wangenheim Prune and P.divaricata seedlings planted in the soil used for fruit tree
crops for at lest 50 years. Folia Univ. Agric. Stetin. Agricultura. 2004. 240(96). P. 87–90.
6. P a c h o l a k E. Replantacja sadów. Sad Nowocz. 2003a. 12. P. 3–6.
7. Pacholak E. Czynniki wywoùujàce chorobê replantacyjnà. Czynniki biotycznenicienie. Sad Nowocz. 2003b. 12. P. 4–5.
8. S i t a r e k M., G r z y b Z. S., K o ù o d z i e j c z a k P. Effect of
rootstocks on growth and yield of plum trees. Journal of Fruit and Ornamental Plant Res.
2001. (Vol. IX), 1–4. P. 19–24.
9. S i t a r e k M., G r z y b Z. S., G u z o w s k a - S p a l e n i a k B., L i s
J. Performance of the rootstocks for plums In two different soil and climatic conditions.
Acta Hort. 2004. 658. P. 273–277.
10. R o z p a r a E., G r z y b Z. S. Growth and cropping twelve plum cultivars
grafted on tworootstocks. Acta Hort. 1994. 359. P. 229–236.
11. R o z p a r a E., G r z y b Z. S. Growth and yield of some plum cultivars
grafted on ‘Wangenheim Prune’ seedlings. Acta Hort. 1998. 478: 91–95.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
292–295.
SKIRTINGØ POSKIEPIØ ÁTAKA ‘DÀBROWICE PRUNE’ VEISLËS SLYVØ
AUGIMUI, DERLIUI IR VAISIØ KOKYBEI NUALINTOJE DIRVOJE
Z. S. Grzyb, M. Sitarek
Santrauka
Jauname sode tirtas ‘Dàbrowice Prune’ veislës slyvø, áskiepytø á du sëklinius
(P. cerasifera var. divaricata Borkh. ir ‘Wangenheimo vengrinë’) ir keturis vegetatyvinius
poskiepius (Jaspi, GF 655/2, Ishtara ir St. Julien A), augimas ir derlius. Slyvos buvo
pasodintos 4,25 x 2,5 m atstumais dirvoþemyje, kuriame maþiausiai 50 metø buvo auginti
vaismedþiai: vyðnios, obelys ir slyvos. Vaismedþiø augimo ir suminio derliaus analizë
parodë, kad slyvos su sëkliniais ‘Wangenheimo vengrinë’ poskiepiais augo prasèiau ir
davë maþesná suminá derliø negu áskiepytos á P. divaricata sëjinukus. Slyvø su sëkliniais
‘Wangenheimo vengrinë’ poskiepiais augimo ir derliaus suprastëjimas, atliekant ðá bandymà,
buvo netipiðkas, palyginti su panaðiø tyrimø rezultatais kitose vietose. Slyvø su kitais
tirtais poskiepiais pakartotinio auginimo problema nebuvo tokia didelë, kaip á
‘Wangenheimo vengrinë’ sëjinukus áskiepytø slyvø.
Reikðminiai þodþiai: slyvos, Prunus domestica L., poskiepiai, veislës, augimas,
derlius, vaisiø masë, persodinimo problemos.
295
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 296–301.
INFLUENCE OF TEN ROOTSTOCKS ON COLD
HARDINESS OF FLOWERS OF CHERRY CULTIVAR
‘BIGARREAU BURLAT’
Valentin LICHEV, Alexandros PAPACHATZIS
Agricultural University, 12 Mendeleev str., 4000 Plovdiv, Bulgaria.
E-mail: [email protected]
After sudden amplitudes in air temperatures in the region of the town of Plovdiv,
Bulgaria, during the winter of 2004–2005 (the daytime values on certain days in January
reached +18°C, while those during the night in the first ten-day period of February were –
18°C) partial frost damages were reported in the flowers of differentiating buds on the
spurs in 9-year-old trees of cherry cultivar ‘Bigarreau burlat’ grafted on 10 rootstocks.
It was established that frost injuries were the most severe (68,6%) in the trees on
Gisela 5, and the least severe (3.3%) in those on P 1 (seedling of P. mahaleb L.). In the rest
of the trees (on Gisela 4, Gi-195/20, Weiroot 10, Weiroot 13, Weiroot 53, Weiroot 72 and
Weiroot 158) they were between 14% and 44%. The trees on Gisela 5 have the greatest
number of flower buds and flowers initiated per unit of length of the two-year-old wood,
but nevertheless, their fruit-bearing in 2005 was the poorest due to frost damages.
Key words: colds, damage, cold hardiness, sweet cherry, rootstocks.
Introduction. The resistance to low winter temperatures is a basic factor for
the successful cherry production in the Baltic and other countries in the North where
temperatures come as low as – 30°C (Janes, 2000).
In more southern countries (including Bulgaria) frost damages of cherry flowers
resulting from winter frosts are more rare phenomenon, whereas damages a as
result of sudden spring frosts are observed comparatively often (Georgiev, 2001).
The degree of frost damages in cherry trees depends on many factors: the way
of its onset, the level of temperature lowering (Georgiev, 2001; Fischer, Hohlfeld,
1998), phenophase and physiological condition of plants, exposure of the land
(Georgiev, 2001), hereditary characteristics of cultivars (Georgiev, 2001; Blazkova,
2004; Fischer, Hohlfeld, 1998; Sitarek, Grzyb, 1998; Janes, 2000), rootstocks
(Koleva, 2001; Blazkova, 2004; Balmer, 1998; Sitarek, Grzyb, 1998) and interstocks
(Rozpara et al., 1997), etc.
The rootstocks of the series Weiroot showed very good hardiness according to
the studies in Germany (Schimmelpfeng, 1996) and as it refers to Gisela, the opinions
of authors differ, but the positive ones predominate. In this connection Franken-
296
Bembenek et al. (1999), Schwarzel, Schneider (1998), find that Gisela 5 has good
hardiness whereas according to Balmer (1998) it defers to wild cherry, mahaleb and
rootstocks of Weiroot series but has a priority over Colt.
Some rootstocks of the Gisela and Weiroot series were introduced in Bulgaria in
the 1995 and were grafted, and the trees obtained in the course of 9 years were
observed in connection with their growth and fruiting. During this period we did not
record extremely cold winters in the region of the experimental field. In the winter of
2004–2005, however, we periodically studied the stages of flower buds
morphogenesis in the experimental trees and established that some of the flowers
developing in them were damaged by frosts. Taking into consideration the lack of
information about the hardiness of these rootstocks under the ecological conditions
in Bulgaria, we carried out research in this field, and the obtained results we present
in this article.
Materials and methods. The trees of the cultivar ‘Bigarreau burlat’, grafted
on rootstocks P 1 (the Bulgarian selection of P. mahaleb L.), Gisela 5, Gisela 4,
Weiroot 10, Weiroot 13, Weiroot 53, Weiroot 72 and Weiroot 158, and also on the
selections of the series Giessen – Gi-195/20 and Gi-497/8, were in the experimental
field in the Department of Fruit growing at the Agricultural University in the town of
Plovdiv, Bulgaria. The plants (6 per variant, distributed using a randomized block
design), were planted in 1996 at distances of 6.0 x 4.5 m, trained as free-growing
crowns, grown under the conditions of herbicide-treated fallow land and were gravity
irrigated.
Frost damage of flower organs has been observed in the third ten-day period of
February in 2005 under laboratory conditions by revealing the lateral buds of the
spurs, collected from trees in advance, under a stereomicroscope. The developing
flowers in the differentiating buds on 24 spurs disposed on two-year-old wood of
the experimental plants were studied from four cardinal points at a height of 2 m
above the ground. In order the estimation of the influence of rootstocks on hardiness
of graft would be more correct, in March of 2005 we did not perform the winter
pruning usual for the previous years, but observed under experimental field conditions
the additional indices, presented below, characterizing some reproductive
characteristics of trees.
Results. During certain periods in the autumn and winter of 2004–2005 the
mean 24-hour air temperature significantly deviated from the mean of the previous
15 years (Fig. 1.). For example, from the beginning until the middle of January in
2005 the temperature was remarkably higher than this of 1990–2004. On 5th and 6th
of January the maximal air temperature reached as high as +18°C which was not
typical for the season. We could assume that this period, which was atypically warm
for the season, caused some physiological processes in the fruit trees leading to their
loss of hardiness.
In the first ten-day period of February in 2005 the opposite tendency was
observed with respect to the mean 24-hour air temperature – the values were lower
than the mean of 15-year transitional period (Fig. 1). At the end of the first ten-day
period of February in 2005 the minimum temperatures continually decreased and in
the course of 6 days their values varied between – 15.5°C and – 18°C.
297
F i g. 1. Mean 24-hour air temperature from September to April during the period
of 1990–2005
1
p a v.
Paros oro temperatûros nuo rugsëjo iki balandþio mën. 1990–2005 m. vidurkiai
The samples collected from the trees during the third ten-day period of February
in 2005 revealed that the flowers in differentiating buds of the graft in separate
variants suffered different degrees of frost damage. The data in Figure 2 indicate
that frost damages in the trees of the Bulgarian rootstock P 1 were rather insignificant
(3.3%), whereas in those on Gisela 5 were 68.6%, and in the remaining ones –
between 13.9% and 44.2%. In the trees on Gisela 5 and Weiroot 72 we observed
frost damages not only in separate flowers within the boundaries of a single fruit
bud, but even individual completely frost damaged buds.
F i g. 2. Influence of the rootstocks on frost damage of flowers in the diferentiating
buds
2
p a v.
Ðalnø daromos þalos, þiedams, pumpurams diferencijuojantis,
priklausomumas nuo poskiepio
The mean 24-hour temperature during the initial ten-day periods of March and
April in 2005 was also significantly lower than the mean of 15-year transitional
period (Fig. 1). Particularly dangerous period for the development of the fruit trees
298
(being in the flower button phase) was the one between 3rd and 6th of April in 2005,
when the absolute minimum temperatures went down as low as – 4.5°C and caused
new damages to the flower organs. During flowering of our experimental trees
(between 8th and 19th of April), we recorded visually new frost damage of flower
organs, but unfortunately it was not possible to report the exact degree of damages
in spring because these damages accumulated at different times in winter and spring.
The number of flower buds and flowers initiated per unit of length of the twoyear-old wood indicates to a great degree fruit-bearing potentiality of plants. In this
connection at the onset of the vegetation in 2005 the trees on Gisela 5, Gi-195/20
and Gisela 4 are distinguished by the highest values (Table). Irrespective of the high
potential productivity of the plants on Gisela 5, the smallest yield was reported for
them in 2005, due to the significant frost damages of their flower organs. The trees
on Gisela 4, Gi-195/20, Gi-497/8 and Weiroot 158 have the highest fruit-bearing
whereas the remaining ones showed average results.
T a b l e. Effect of rootstock on some reproductive behaviours of sweet
cherry trees during 2005
L e n t e l ë.
Rootstocks
Poskiepiai
P1
Gisela 5
Gisela 4
Gi-195/20
Gi-497/8
Weiroot 10
Weiroot 13
Weiroot 53
Weiroot 72
Weiroot 158
LSD0.5
Poskiepio átaka treðniø þydëjimui ir derliui 2005 m.
Number of flower buds per
linear meter
Number of flowers per
linear meter
Þiedø skaièius linijiniame
metre
Yield of crown
Vainiko derlius,
kg/m3
22.6
123.4
81.7
116.5
43.6
24.2
14.5
19.8
57.8
28.7
46.1
493.8
204.7
352.5
145.4
78.3
47.8
68.7
169.0
99.0
1.28
0.54
2.18
2.14
1.98
1.45
1.40
1.37
1.32
1.81
23.1
72.6
0.65
Þiedø pumpurø skaièius linijiniame
metre
Discussion. The winter frost damages recorded by us were to a great degree
unexpected, particularly taking into consideration Georgiev’s opinion (2001) that
under the climatic conditions of Bulgaria, damages of the flowers of cherry trees
were observed at air temperatures lower than –23–25°C. According to us the main
reason of frost damages in the winter of 2005 were rather big amplitudes in air
temperatures in December and particularly in January as compared to those at the
end of the first ten-day period of February. This probably led to the untimely onset
of some initial physiological processes accompanying the transition from dormancy
to vegetation when the hardiness of all tree parts (including their flowers), decreased
significantly. After such big temperature amplitudes during the winter months in
299
Germany, Fischer and Hohlfeld (1998) also observed frost damages in a great number
of cherry cultivars.
In maintenance of our statement that after winter frosts, the experimental trees
were also additionally damaged by late spring frosts, was Georgiev’s opinion (2001)
that air temperatures from – 1.7 to – 5.5°C were crucial for the development of
cherry plants in flower button phase. Other authors, both in Bulgaria (Blagov et al.,
2004) and abroad as well (Pieber, Modl, 1997), also observed frost damages of
flower organs under similar climatic conditions as a result of lowering of temperature
to – 6°C immediately before the flowering of cherry trees.
Conclusions. After sudden amplitudes in air temperatures during the winter of
2004–2005 (the daytime values on certain days in January reached + 18°C, while
those at night in the first ten-day period of February came down to – 18°C) partial
frost damages were reported in the flowers of differentiating buds on the spurs in
9-year-old trees of cherry cultivar ‘Bigarreau burlat’ grafted on 10 rootstocks.
It was established that frost injuries were most severe (68.6%) in the trees on
Gisela 5, and the least severe (3,3%) in those on P 1 (seedling of P. mahaleb L.). In
the rest of the trees (on Gisela 4, Gi-195/20, Weiroot 10, Weiroot 13, Weiroot 53,
Weiroot 72 and Weiroot 158) they were limited between 14% and 44%. The trees on
Gisela 5 have the greatest number of flower buds and flowers initiated per unit of
length of two-year-old wood, but nevertheless, their fruit-bearing in 2005 was the
smallest due to frost damages. During the same year the plants on Gisela 4,
Gi-195/20, Gi-497/8 and Weiroot 158 were distinguished by their highest yield per
1 m3 of the crown volume.
Gauta
2006 05 04
Parengta spausdinti
2006 07 17
References
1. B a l m e r M. Sûsskirschenunterlagen in Bewegung. Deutsche Baumschule.
1998. 10. P. 37–39.
2. B l a g o v A., M i l e n k o v M., C h r i s t o v N. The late spring frosts
and their influence under fruit tree cultivars. Plent Science. 2004. 41. P. 11–13.
3. B l a z k o v a J. Resistance to abiotic and biotic stressors in sweet cherry
rootstocks and cultivars from the Czech republic. Journal of Fruit and Ornamental Plant
Research. 2004. Vol. 12. P. 303–310.
4. F i s c h e r M., H o h l f e l d B. Wie frosthart sind Sûsskirschen? Obstbau.
1998. 5. 262–265.
5. F r a n k e n - B e m b e n e k S., G r u p p e W., L i n k e G., S c h m i d t
H. Ruckblick auf das Zuchtungsprogramm der Gisela – Kirschenunterlagen.
Erwerbsobstbau. 1999. 41. P. 123–128.
6. G e o r g i e v V. Ecological requirements. In: Georgiev V., Borovinova M., Koleva
A. Cherry, Zemizdat, Sofia, 2001. P. 40–61.
7. J a n e s H. Research results of sweet cherry cultivars and selections testing at
the Polli horticultural institute. Plodovodstvo. 2000. 13. P. 214–216.
300
8. K o l e v a A. Rootstocks. In: Georgiev V., Borovinova M., Koleva A. Cherry,
Sofia, 2001 P. 186–207.
9. P i e b e r K.,
M o d l P. Doch Blûtenfrostschãden an den Obstgehõlzen.
Besseres Obst. 1997. 7. 10 p.
10. R o z p a r a E., G r z y b Z., Z d y b H. Growth and fruiting of two sweet
cherry cultivars with different interstems. Acta Hort. 1997. 468. P. 345–352.
11. S c h i m m e l p f e n g H. Unterlagenzûchtung fûr Sûsskirschen in
Deutschland – die Weihenstephaner Arbeiten. Schweiz. Z. Obst – Weinbau. 1996. 13.
P. 331–334.
12. S c h w ä r z e l H., S c h n e i d e r U. Leistung neuer Sorten – Unterlagen
– Kombinationen bei der Sûsskirsche. Deutsche Baumschule. 1998. 11. P. 32–34.
13. S i t a r e k M., G r z y b Z. Frost injuries of sweet cherry and plum after
winter 1996/97. Journal of Fruit and Ornamental Plant Research. 1998. 6.1. P. 15–22.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
296–301.
DEÐIMTIES POSKIEPIØ ÁTAKA ‘BIGARREAU BURLAT’ VEISLËS VYÐNIØ
ÞIEDØ ATSPARUMUI ÐALÈIAMS
V. Lichev, A. Papachatzis
Santrauka
Po staigiø oro temperatûros svyravimø Plovdiv miestelio (Bulgarija) rajone
2004–2005 metø þiemà (kai kuriomis sausio dienomis temperatûra pakildavo iki +18°C, o
pirmàjá vasario deðimtadiená naktimis nukrisdavo iki – 18°C) buvo pastebëta, kad ðalnos ið
dalies apðaldë 9 metø ‘Bigarreau burlat’ veislës vyðniø, áskiepytø á 10 poskiepiø,
besidiferencijuojanèiø pumpurø þiedus.
Nustatyta, kad ðalèiai labiausiai (68,6%) paþeidë vyðnias, áskiepytas á Gisela 5,
maþiausiai (3,3%) – á P 1 (P. mahaleb L. sodinuko) poskiepá. Kiti vaismedþiai (áskiepyti á
Gisela 4, Gi-195/20, Weiroot 10, Weiroot 13, Weiroot 53, Weiroot 72 ir Weiroot 158) buvo
paþeisti 14–44%. Á Gisela 5 áskiepytos vyðnios sukrovë daugiausia þiedø pumpurø, bet dël
ðalnø 2005 metais jø derlius buvo prasèiausias.
Reikðminiai þodþiai: ðalèiai, þala, atsparumas ðalèiams, vyðnios, poskiepiai.
301
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 302–315.
STUDIES ON GENETIC VARIATION IN WILD CHERRY
USING RAPD ANALYSIS
Yu-Liang CAI 1,2, Gui-Fang ZHAO 2, Dong-Wei CAO 2
1
College of Horticulture, Northwest A & F University, Yangling 712100,
P.R.China
2
School of Life Science, Northwest University, Xi’an 710069, P.R.China
Random amplified polymorphic DNA (RAPD) variation among 8 cherry species and
2 interspecific progenies were analyzed. 48 arbitrary oligonucleotide primers out of 130
were screened for PCR amplification to generate polymorphisms. The phylogenetic analysis
was carried out using two distance-matrix methods and a dendrogram was generated to
show the relationships among species and cultivars. The results showed that there were
840 amplified loci in total; 23 sweet cherry and 4 sour cherry cultivars were clustered
together with 569 and 247 polymorphic loci, respectively, which accounted for 67.74% and
29.40% of the total variation. P. tomentosa T., P. fruticosa var. aucta P. and P. humilis B.
formed a monophyletic group. A relationship between P. pseudocerasus L. and Colt, which
formed another closely related group, was observed while P. avium L., P. cerasus L. and
other cherry species were more divergent. The range of genetic distance was from 0.0623
to 0.2719 among the Prunus species, which were genetically distinct. The topology of the
tree was generally in agreement with taxonomic classification. The results indicated that
with the exception of the sweet cherry cultivar ‘Hongdeng’, there were one or more cultivarspecific RAPD markers in cherry species and cultivars. Using these specific markers,
cherry species and cultivars could be identified and there is therefore the potential to
select for good characteristics of hybrids at an early stage.
Key words: cherry, RAPD, species, genetic relationship.
Introduction. Cherries have been classified within the genus Prunus, which is
part of the family Rosaceae (Ingram, 1948; Rehder, 1974), while Yu (1986) placed
cherries within the genus Cerasus. We have adopted the former taxonomical system
in this paper. Compared with other temperate fruits, cultivated cherries have great
unfulfilled market potential (Webster 1996). However, in China, for example, there
still exists the problem of homonyms and synonyms in the cultivated cherry cultivars
or rootstocks because of bud variability or misuse of like-named cultivars and rootstock
seedlings in cherry production, which can lead to a significant reduction in commercial
returns.
There are rich wild cherry germplasm resources in the mountain areas of China,
302
but few data are available on the natural levels of genetic variation in the wild cherry
species, Random amplified polymorphic DNA are useful as genetic markers (Williams
1990), and RAPD analysis offers a rapid, cheap and stable means of producing a
genetic profile for horticultural crops (Hormaza, 1999; Jordano and Godoy, 2000;
Luo et al., 2001; Malusa and Marchesini, 1996; Wang et al., 2002). Gerlach and
Stosser (1998) studied 18 sweet cherry cultivars and found unique RAPD markers
of 14 of these cultivars. Stockinger (1996) constructed a linkage map for the sweet
cherry cultivar ‘Emperor Francis’ from a population of 56 microspore-derived callus
culture individuals and amplified a region of the ‘Emperor Francis’ genome containing
a unique sequence based on RAPD analysis. However, these studies did not extend
to distinguishing between sour cherry varieties.
In our study, we also analyzed sweet cherry cultivars that were different from
the varieties used by Gerlach and Stosser (1998) except cherry cultivar ‘Hedelfinger’.
Zhou (2002) used AFLP analysis to estimate the genetic distance and relationships in
a sweet cherry breeding population while Boritzki (2000) used AFLP and microsatellite
markers to identify cherry accessions. Some cherry cultivars with identical
morphological characters and previously treated as one cultivar can be separated on
the basis of isozyme genotype (Granger et al., 1993). Our main objectives were to
study genetic variation among wild cherry species and to find specific RAPD markers
that are useful to distinguish between cultivars or to describe a certain cultivar uniquely.
Materials and methods. F i e l d s a m p l i n g. Fresh leaves of 8 cherry
species and two interspecific progenies were sampled in 2003–2004 from a collection
held in the Northwest Sci-Tech University of Agriculture and Forestry (NWSUAF)
(34°132 N, 109°52 E) with loam and loess soil. Materials were sampled from adult
productive trees, four wild cherry species were collected from the following
locations: P. pseudocerasus (33°342 N, 107°482 E), P. maximowiczii (41°182 N,
124°42 E), P. humilis (27°92 N, 100°152 E), P. tomentosa (33°342 N, 107°482 E).
23 sweet cherry and four sour cherry cultivars, two interspecific progenies,
P. serrulata var. lannesiana and P. mahaleb in the collection have been sourced as
budwood from overseas germplasm repositories or other government research station
collections. The cultivars and accessions were propagated using the chip budding
method. Table 1 lists those species, cultivars or accessions held in the NWSUAF
collection and sampled for RAPD analysis. Accessions that have unknown parentage
are indicated by the place of origin. Five clonal plants of each accession were
propagated and selected for sampling. Young unfolded leaves were collected from
individual trees, stored in an icebox and transported to the laboratory immediately.
The leaf samples were frozen at -80°C before use.
D N A e x t r a c t i o n a n d a m p l i f i c a t i o n. DNA isolation for
PCR-RAPD analysis followed the procedure of Hormaza (1999). Approximately 0.2g
of fresh leaves were ground in a 1.5 ml Eppendorf tube with 320 µl of extraction
buffer (100mM Tris- HCl, 1.4M NaCl, 20 mM EDTA (pH 8.0), 2% CTAB, 1% PVP,
0.2% â-mercaptoethanol). The samples were incubated at 65°C for 1 h, mixed with
an equal volume of chloroform-isoamyl alcohol (24:1) and centrifuged at 15 000 G
for 10 min, and the above step was repeated one more time. 200µl of the supernatant
was transferred to a new tube and DNA was precipitated by the addition of 400µl
303
cold dehydrated alcohol at -20°C for 1 h. The nucleic acid precipitate was recovered
by centrifugation at 12 000 G for 6 min, washed in 400µl of 10 mM ammonium
acetate in 70% alcohol overnight at 4°C, then dried overnight and resuspended in
200µl of modified TE buffer (10mM Tris-HCl, 0.1 mM EDTA, pH8.0). The
concentration and purity of extracted DNA were assessed spectrophotometrically
(Biophotometer, Eppendorf, Germany), diluted to 15 ng·µl-1 and used for PCR
amplification.
T a b l e 1.
1
Species, cultivars or accessions of cherry evaluated in the
phylogenetic analysis and their origins
l e n t e l ë. Filogenetiðkai ávertintos vyðniø rûðys, veislës arba selekciniai
numeriai ir jø kilmë
Cultivar
No.
Veislës Nr.
Species belonged Cultivar or accession
Rûðys
Origin
Veislë arba selekcinis
numeris
Kilmë
1
P. avium
‘Valerif’
Hungary / Vengrija
2
P. avium
‘Solymari’
Hungary / Vengrija
3
P. avium
‘Hedelfinger’
Germany / Vokietija
4
P. avium
‘Utah Giant’
USA / JAV
5
P. avium
‘Celeste’
Van × New Star
6
P. avium
‘Germersdorfer 3’
Hungary / Vengrija
7
P. avium
‘Germersdorfer 45’
Hungary / Vengrija
8
P. avium
‘Napoleon’
Germany / Vokietija
9
P. avium
‘Sunburst’
Van × Stella
10
P. avium
‘Hongdeng’
Napoleon × Governor Wood
11
P. avium
‘Sato Nishiki’
Governor Wood × Napoleon
12
P. avium
‘Katalin’
Germersdorfer × Podjebrad
13
P. avium
‘Governor Wood’
USA / JAV
14
P. avium
‘Linda’
Hedelfinger × Germersdorfer
15
P. avium
‘Hongfeng’
Yantai, Shandong
16
P. avium
‘Marjit’
Germersdorfer3 × Bekescsaba
17
P. avium
‘Jaboulay’
Hungary / Vengrija
18
P. avium
‘Black Tartarian’
Russia / Rusija
19
P. avium
‘Longguan’
Open-pollinated Black Tartarian
20
P. avium
‘Lapins’
Van × Stella
21
P. avium
‘Van’
Seedling of Empress Eugenie
Empress Eugenia sëjinukas
22
P. avium
‘Sam’
Seedling of V160140 / V160140 sëjinukas
23
P. avium
‘Rainier’
Bing×Van
24
P. mahaleb
C500
Hungary / Vengrija
304
T a b l e 1 continued
1
l e n t e l ë s tæsinys
Cultivar
No.
Veislës Nr.
Species belonged Cultivar or accession
Rûðys
Origin
Veislë arba selekcinis
numeris
Kilmë
25
P. cerasus
‘Meteor Korai’
Pandy × Nagy Angol
26
P. cerasus
‘Favorit’
Hungary / Vengrija
27
P. cerasus
‘Ujfehertoi Furtos’
Hungary / Vengrija
28
P. cerasus
‘Kantorjanosi’
Hungary / Vengrija
29
P. avium ×
‘Colt’
P. pseudocerasus
P. avium × P. pseudocerasus
30
P. pseudocerasus ‘Qinling Manao’
Fuoping, Qinling mountains Shaanxi
province / Fuoping, Qinling kalnai, Shaanxi
31
P. maximowiczii ‘Heiyingtao’
Benxi, Liaoning province / Benxi, Liaoning
32
P. serrulata
var. lannesiana
E1-3
Japan / Japonija
33
P. fruticosa
var. aucta
‘Prob’
P. mahaleb×P. fruticosa
34
P. humilis
‘Lijiang Ouli’
Lijiang, Yunnan province / Lijiang, Yunnan
35
P. tomentosa
‘Fuoping
Maoyingtao’
Fuoping, Qinling mountains Shaanxi
province / Fuoping, Qinling kalnai, Shaanxi
provincija
provincija
provincija
provincija
One hundred and thirty RAPD primers (Operon Technologies Inc., USA) were
used for initial screening against the three cultivars and accessions with the highest
heterozygosity based on the previous research (Webster et al., 1996; Yu, 1986) to
identify polymorphic RAPD markers, we selected 48 primers listed in Table 2 from
130 ten bp-primers. DNA amplification reactions were performed in volumes of
20 µl as described by Williams et al. (1990), with some modifications, containing
10y!buffer (10 mM KCl, 8 mM (NH4)2SO4, 10 mM Tris-HCl, pH 9.0, 0.08% Nonidet
P40), 1.9mM MgCl2, 0.2mM each of dATP, dCTP, dGTP and dTTP, 30ng of genomic
DNA, 0.28 µM primer and 2 U of Taq DNA polymerase (Sangon Shanghai) overlaid
with 20 µl mineral oil. PCR reactions were carried out in a T Gradient (Biometra®)
thermocycler programmed for an initial denaturation step of 96°C for 5 min 30 sec,
followed by 40 cycles of 1 min 30 sec at 94°C, 1 min at 40°C, and 2 min at 72°C.
The reaction was completed with a final run at 72°C for 10 min. Following
amplification, the samples were stored at 4°C prior to electrophoresis. Amplified
DNA fragments were analyzed by gel electrophoresis in 1.6% agarose gels in 1y!
TAE buffer and detected by staining with 0.5µg·ml-1 ethidium bromide. Gels were
run for 3 h at 50 mA and visualized under UV light (Kodak Scientific Imaging Systems,
USA).
305
D a t a a n a l y s i s. Each sample was amplified at least twice to verify
reproducibility. Only those RAPD markers that reproduced consistently across
successful PCR reactions and across DNA extractions were included in the analysis.
Amplification products were scored as “present” or “absent” and transferred to a
binary code with 1 or 0, respectively. A data matrix of individual marker containing
the band scoring information was transformed to allele frequencies under the
assumption that each amplified band corresponds to different RAPD locus. This
dataset was used to calculate the percentage of polymorphic loci, genetic distance
and genetic identity (Nei’s unbiased distance estimate; Nei, 1978) among species
and cultivars using the POPGENE 32 package. A dendrogram was constructed based
on Nei’s genetic distance using the unweighted pair-group mean analysis (UPGMA)
method modified from Neighbor procedure of PHYLIP version 3.5 and the Neighborjoining method (NJ). The significance was tested using a PAUP 4.0 package with the
bootstrap test program of Felsenstein (Felsenstein, 1985), and resampled with
n = 1000 randomizations. Euclidean distances were estimated using a program of
Statistica version 6.0 and a similar dendrogram was also constructed by using the
UPGMA method. The specific bands (markers) useful for identifying genotypes
were followed by the approximate number of base pairs of the amplified fragment.
Results. Out of 130 primers, 48, summarized in Table 2, were informative, as
they generated clear, polymorphic fragments among the investigated genotypes. We
analyzed a total of eight cherry species and two interspecific progenies with
35 varieties and accessions, 5 cloned individuals of each cultivar and accession
propagated by chip budding were also analysed using the PCR-RAPD method. Each
primer generated a specific RAPD profile. An example of RAPD pattern, obtained
with the primers of OPY20 and OPB07, are shown in Fig.1 and Fig.2, respectively.
A total of 838 polymorphic amplification products were generated in the range of
100-2977 bp. For the five chip budded individuals of each cultivar or accession
tested, we tested five clones of the cultivar “Van” (data not shown), and each of the
48 primers generated a monomorphic PCR-RAPD pattern, which indicated that the
method of asexual reproduction (grafting propagation) did not affect the genetic
structure of the clonal plants.
S p e c i f i c R A P D m a r k e r s a m o n g t h e g e n o t y p e s.
The 48 primers amplified a total of 569 DNA polymorphic loci for the 23 sweet
cherry cultivars, the amplified DNA fragments ranging from 100 to 2977 bp, and the
percentage of polymorphic loci was 67.74%. 83 amplified DNA fragments were
unique to sweet cherry genotypes (Table 3).
A total of 247 DNA polymorphic loci were amplified for the four sour cherry
cultivars and the amplified DNA fragments ranged from 100 to 2533 bp, while the
percentage of polymorphic loci was 29.40%. 13 specific RAPD markers were
amplified for the sour cherry (Table 3).
It was evident that, with the exception of the sweet cherry variety ‘Hongdeng’,
there were one or more specific RAPD markers amplified for cherry cultivars and
accessions in Table 3 (the number of accessions being the same as the number of
accessions in Table 1). The numbers of specific RAPD markers varied in the different
genotypes. The accession P. pseudocerasus showed specific RAPD markers with
OPA07, OPB13, OPD15, OPD20 and OPY20. The accession P. mahaleb showed
specific RAPD marker with OPA09. The accession P. serrulata var.lannesiana
306
showed specific RAPD markers with OPAI01, OPA09, OPB07, OPC13 and OPG16.
The accession P. maximowiczii showed specific RAPD marker with OPB12. The
accession P. humilis showed specific RAPD markers with OPAI01, OPC15 and
OPD11. The accession P. tomentosa showed specific RAPD marker with OPD11.
The interspecific progeny “Colt” showed specific RAPD markers with OPA19,
OPAD16, OPD15 and OPD20 and the interspecific progeny “Prob” showed specific
RAPD marker with OPG19.
T a b l e 2. RAPD primers used in the survey of the number of
amplified products of cherry
2
l e n t e l ë. Dauginant vyðnias naudoti RAPD pradmenys
Primer
Žymuo
Sequence
Primer
Sequence
Primer
Sequence
(5'–3')
Seka (5'–3')
Žymuo
Seka (5'–3')
Žymuo
OPB01
GTTTCGCTCC
OPD02
GGACCCAACC
OPH15
AATGGCGCAG
OPB07
GGTGACGCAG
OPD04
TCTGGTGAGG
OPH20
GGGAGACATC
OPB08
GTCCACACGG
OPD08
GTGTGCCCCA
OPY20
AGCCGTGGAA
OPB12
CCTTGACGCA
OPD11
AGCGCCATTG
OPK01
CATTCGAGCC
OPB13
TTCCCCCGCT
OPD15
CATCCGTGCT
OPO06
CCACGGGAAG
OPB17
AGGGAACGAG
OPD16
AGGGCGTAAG
OPQ07
CCCCGATGGT
OPA01
CAGGCCCTTC
OPD20
ACCCGGTCAC
OPAH20
GGAAGGTGAG
OPA07
GAAACGGGTG
OPC07
GTCCCGACGA
OPAI01
GGCATCGGCT
OPA08
GTGACGTAGG
OPC13
AAGCCTCGTC
OPAI20
CCTGTTCCCT
OPA09
GGGTAACGCC
OPC15
GACGGATCAG
OPAO15
GAAGGCTCCC
OPA10
GTGATCGCAG
OPG02
GGCACTGAGG
OPAQ03
GAGGTGTCTG
OPA12
TCGGCGATAG
OPG06
GTGCCTAACC
OPAD04
GTAGGCCTCA
OPA13
CAGCACCCAC
OPG16
AGCGTCCTCC
OPAD08
GGCAGGCAAG
OPA19
CAAACGTCGG
OPG18
GGCTCATGTG
OPAD11
CAATCGGGTC
OPA20
GTTGCGATCC
OPG19
GTCAGGGCAA
OPAD13
GGTTCCTCTG
OPD01
ACCGCGAAGG
OPH13
GACGCCACAC
OPAD16
AACGGGCGTC
Seka
V a r i a t i o n a m o n g c h e r r y s p e c i e s. Total genetic distance
estimates ranged in value from 0.0623 to 0.2719 among the cherry species studied
which were genetically distinct, with a mean genetic distance of 0.1758. Table 4
summarizes the genetic distance (GD) and genetic identity (GI) statistics based on
Nei’s unbiased estimate (Nei 1978) and showed the maximum genetic distance was
between P. mahaleb and Colt (GDmax=0.2719) followed by a genetic distance of
0.2626 between P. pseudocerasus and P. humilis. The minimum genetic distance
was between P. avium and P. cerasus (GDmin=0.0623). On the other hand, the
minimum genetic identity was between P. mahaleb and Colt (GImin=0.7619) and the
maximum genetic identity was between P. avium and P. cerasus (GImax=0.9396),
with an average genetic identity of 0.8400 among the cherry species; this result is
consistent with the analysis of genetic distance.
307
T a b l e 3. Specific RAPD markers among 34 cherry genotypes
3
l e n t e l ë.
Accession
No.
Selekcinis Nr.
Specifiniai RAPD þymenys tarp 34 vyðniø genotipø
Primers revealing specific RAPDs (No. of base pairs of a band)
Þymenys, atskleidþiantys specifinius RAPD (pagrindiniø grupës porø Nr.)
1
B01 (1226), H20 (1231), K01(326), K01 (1400)
2
C13 (2631), C13 (2977), K01 (1333)
3
A08 (500), D11 (325), D11 (1023)
4
AD13 (889), A01 (978), A01 (1925), C07 (1113), G02 (825)
5
AD11 (1000), A01 (1461), B12 (2298), B13 (341), G18 (2700)
6
AD11 (934), B12 (1390), C13 (519), D02 (252), D08 (297)
7
AD11 (1971), A01 (1700), D08 (1095), G06 (368), H20 (1108)
8
C07 (357)
9
A10 (830), A01 (2222)
11
D04 (673)
12
AO15 (291), C07 (1113), D04 (456), D04 (800), H20 (1800)
13
A10 (592), B07 (1725)
14
C13 (2377), K01 (592)
15
A20 (860), A07 (663), B17 (800), D20 (472), G16 (265), H20 (1277), Y20 (300)
16
AD11 (667), A01 (675), A01 (781), G02 (1746), Y20 (426)
17
B01 (715), B01 (1040), B08 (600), G02 (925)
18
A10 (675), A10 (1517), AO15 (351), D15 (2744)
19
A10 (1718), B13 (554), B01 (1278), C07 (975), D08 (465), Y20 (254)
20
D04 (300), G16 (347), H20 (1462)
21
A09 (829), D04 (413), G06 (472), G16 (659)
22
B01 (2111), D15 (925), G02 (250), Y20 (249)
23
A19 (1200), AH20 (1132), G02 (397)
24
A09 (987)
25
A20 (425), AD11 (731), AI01 (1145), AI01 (2000), AQ03 (441), D02 (1500), D02
(1200), G02 (635)
26
AI20 (2533)
27
A07 (1048), K01 (1033)
28
A08 (285), H13 (1503)
29
A19 (294), AD16 (300), D15 (550), D15 (675), D15 (1173), D20 (850)
30
A07 (1754), B13 (1411), D15 (190), D20 (790), Y20 (1400)
31
B12 (805)
32
AI01 (552), A09 (1627), B07 (553), B07 (758), C13 (300), G16 (261)
33
G19 (227)
34
AI01 (750), C15 (550), D11 (934)
35
D11 (538)
308
F i g. 1. RAPD pattern amplified by primer OPY20
1 p a v. RAPD pavyzdys, padaugintas OPY20 pradmeniu
From left to right (lane) in order: M: DNA marker, 100bp DNA Ladder , numbers refer to the
cultivars listed in Table 1. / Ið kairës á deðinæ (juostelës): M: DNR þymuo, 100bp DNR þemëlapis,
skaièiai rodo 1 lentelëje iðvardytas veisles.
F i g. 2. RAPD pattern amplified by primer OPB07
2 p a v. RAPD pavyzdys, padaugintas OPB07 pradmeniu
From left to right (lane) in order: M: DNA marker, 100bp DNA Ladder, numbers refer to the
accessions and cultivars listed in Table 1. / Ið kairës á deðinæ (juostelës): M: DNR þymuo, 100bp DNR
þemëlapis, skaièiai rodo 1 lentelëje iðvardytas veisles.
Cluster analysis of genetic distance among
c h e r r y s p e c i e s. Based on Nei’s genetic distance, the following dendrogram
(Fig. 3) was generated by adopting the UPGMA method modified by the NEIGHBOR
procedure of PHYLIP Version 3.5. The bootstrap resampling process was repeated
1000 times, allowing the construction of consensus tree according to the rule of
50% majority (Nei et al., 2000). Clades, with bootstrap values (Nei et al., 2000)
higher than 50%, are indicated in bold. The phylogenetic tree obtained by using
UPGMA was consistent with that obtained by using the NJ method in describing
relationships between species or cultivars. The topology of the tree was generally in
agreement with taxonomical classification.
As indicated in Fig.3, there was a clear separation between P. avium (nos1-23,
shown in Table 1) and the other species in the study, the significance (bootstrap
value) was 100%. 23 cultivars of P. avium clustered into a large group, revealing a
relatively closer relationship among these cultivars.
P. pseudocerasus (30) and ‘Colt’ (29) formed a single group (96% significance),
309
and were separated from P. cerasus (25-28), P. serrulata var. lannesiana (32),
P. mahaleb (24), P. maximowiczii (31), P. humilis (34), P. fruticosa var. aucta (33)
and P. tomentosa (35). Four cultivated varieties (25, 26, 27 and 28) of P. cerasus
formed a closely clustered group and were separated from the species indicated by
the numbers 32, 24, 31, 34, 33 and 35 (67% significance).
T a b l e 4. Analysis of genetic distance (below diagonal) and genetic
identity (above diagonal) based on Nei’s gene diversity
index
l e n t e l ë. Genetinio skirtingumo (po ástriþaine) ir genetinio tapatumo (virð
ástriþainës) analizë, remiantis Nei genø skirtingumo indeksu
0.8202
0.8226 0.8214 0.8286
P. cerasus
0.0623 0.1362 * * * 0.8601 0.8602
0.8840
0.8720
0.9116 0.8912 0.8909
Colt
0.1848 0.2719 0.1507 * * *
0.8143
0.7917
0.7940
0.8107 0.7810 0.7881
***
0.7845
0.7940
0.7869 0.7690 0.7929
***
0.8238
0.8643 0.8393 0.8464
P. serru0.1559 0.1982 0.1370 0.2306 0.2306
lata var.
lannesiana
0.1938
***
0.8190 0.8012 0.8298
P. fruticosa
0.0733 0.1953 0.0925 0.2098 0.2396
var. aucta
0.1459
0.1996
***
P. humilis
0.1183 0.1967 0.1152 0.2472 0.2626
0.1752
0.2217
0.1200
P. tomentosa
0.1060 0.1881 0.1155 0.2381 0.2321
0.1667
0.1866
0.1040 0.1349
P. pseudo0.1809 0.2534 0.1506 0.2054
cerasus
P. maximowiczii
0.1251 0.2069 0.1233 0.2336 0.2427
P. tomentosa
0.8131
P. humilis
P. mahaleb 0.1509 * * * 0.8726 0.7619 0.7762
P. fruticosa var.
aucta
P. serrulata var.
lannesiana
0.9293 0.8884 0.8994
Colt
0.8556
P. avium
P. cerasus
0.8824
Rûðys
P. mahaleb
* * * 0.8599 0.9396 0.8313 0.8345
Species
P. avium
P. maximowiczii
P. pseudocerasus
4
0.8869 0.9012
***
0.8738
***
P. serrulata var. lannesiana (32) was separated from the species indicated by
the numbers 24, 31, 34, 33 and 35 (62% significance).
P. mahaleb (24) was separated from the species numbered 31, 34, 33 and 35
(65% significance). The genotypes of P. tomentosa (35) and P. fruticosa var. aucta
(33) first clustered into a clade, then formed the second clade with P. humilis (34).
The bootstrap value for the clade that distinguished P. tomentosa, P. fruticosa var.
aucta and P. humilis from P. maximowiczii (31) was 57%.
Among the cultivated varieties of P. avium (Fig. 3), by adopting 11.60 as the
threshold value of branch length between the cherry species based on Nei’s genetic
distance (Nei 1978), these cultivars could be categorized into 5 clusters.
310
3
F i g . 3. Cluster analysis of phylogenetic relationships among
8 cherry species and 2 interspecific progenies
p a v. 8 vyðniø rûðiø ir 2 tarprûðiniø hibridø filogenetiniø santykiø bendra analizë
(Accession and cultivar numbers refer to the accessions and cultivars listed in Table 1. The
boldface numbers are the percentage of times the monophyletic group occurred in 100 bootstrap
samples.) / (Selekciniai ir veisliø numeriai atitinka 1 lentelëje iðvardytus selekcinius numerius ir veisles.
Paryðkinti skaièiai – tai monofiletinës grupës procentai 100-e jungtiniø pavyzdþiø.)
311
The first cluster included 9 cultivars, and could be further classified into three
subclusters, the first subcluster comprised the five cultivars ‘Sunburst’ (no.9 in
Table 1), ‘Hongdeng’ (10), ‘Sato Nishiki’ (11), ‘Governor Wood’ (13) and ‘Rainier’
(23); the second subcluster comprised the three cultivars ‘Marjit’ (16), ‘Linda’ (14)
and ‘Hongfeng’ (15) while the third subcluster corresponded to the cultivar ‘Black
Tartarian’ (18).
The second cluster included 7 cultivars, further classified as two subclusters,
the first of which included the cultivars ‘Valerif’ (1) and ‘Solymari’ (2) while the
second subcluster was composed of the cultivars ‘Germersdorfer 3’ (6), ‘Napoleon’
(8), ‘Hedelfinger’ (3), ‘Utah Giant’ (4) and ‘Celeste’ (5).
The third cluster comprised four cultivars, further classified as two subclusters.
The first of these corresponded to the variety ‘Sam’ (22), while the second subcluster
included the cultivars ‘Van’ (21), ‘Jaboulay’ (17) and ‘Lapins’ (20).
The fourth cluster comprised the cultivars ‘Germersdorfer 45’ (7) and ‘Katalin’
(12) while the fifth cluster corresponded to the cultivar ‘Longguan’ (19).
The above results indicated that the cluster relationships between cherry species
were well supported. With the exception of P. tomentosa, ‘Prob’ and P. humilis,
bootstrap values were all higher than 50%. P. tomentosa, ‘Prob’ and P. humilis had
a close relationship and formed a monopheletic group. This single group clustered
into a new group with P. maximowiczii, P. mahaleb, P. serrulata var. lannesiana,
P. cerasus, P. pseudocerasus and ‘Colt’ and the latter group formed a significantly
larger group with P. avium. The phylogenetic tree has clearly revealed the mutual
relationships among eight cherry species and two interspecific hybrids during the
phylogenetic evolutionary process.
Discussion and conclusions. I d e n t i f i c a t i o n o f c h e r r y
cultivars
and
genetic
relationship
among
c u l t i v a r s. The 816 loci, with high polymorphism, were detected by using 48
primers to perform PCR amplification on all the P. avium and P. cerasus cultivars.
Characteristic loci, which can be used for rapid cultivar identification, were amplified
in all the cultivars except ‘Hongdeng’. Previous studies have revealed that
characteristic bands can be ultimately detected by enlarging the quantity of primers
(Wang et al., 2002). In theory, this rule also applies to cultivar “Hongdeng”. This
research has indicated that, as an important molecular marker, RAPD technique can
be applied to the identification of cherry cultivars and early screening of specific
characters of selections, which provide a theoretical basis for the identification of
homonyms and synonyms in cherry. This result is in agreement with previous studies
on cherry and other fruit species (Gerlach et al., 1998; Huang et al., 2003; Luo et al.,
2001; Stockinger et al., 1996).
As shown by the dendrogram, 23 cultivars of P. avium clustered into a large
group, as did the four cultivars of P. cerasus, which complies with the classic
taxonomy (Webster et al. 1996; Yu 1986). In the phylogenetic tree, cherry cultivars
with closer mutual relationships and similar pomological characters mostly clustered
into a group. However, since most of the varieties are hybrids or natural mutants,
they have relatively complex genetic backgrounds. By adopting the genetic distance
11.60 as the threshold value, the cultivars of P. avium studied can be categorized
312
into 5 groups. Taking as an example the 5 cultivars in the first subgroup of the first
group, ‘Sato nishiki’ (11), ‘Governor Wood’ (13) and ‘Rainier’ (23), all have a yellow
pericarp and have a close genetic relationship with ‘Sunburst’ (9) and ‘Hongdeng’
(10), to form a cluster. In the cultivars’ clustering tree, on one hand, ‘Hongdeng’
(10) and ‘Sato nishiki’ (11) share the common parent ‘Governor Wood’ (13), while
‘Sunburst’ (9) and ‘Rainier’ (23) have ‘Van’ (21) as their common parent (Webster
et al. 1996). On the other hand, although ‘Sunburst’ and Rainier’ share the common
parent ‘Van’, they failed to cluster into a group with ‘Van’. It is suggested that the
other parents, which affect the clustering result among these cherry varieties, had
played a more important role in their respective genetic constitutions.
Phylogenetic relationships among wild cherry
s p e c i e s. The topology of the tree was generally in agreement with taxonomic
classification in this study. According to the classic taxonomy, P. tomentosa (35)
and P. humilis (34) have been listed in subgenus Microcerasus Webb (Rehder 1974).
In this study, these two species clustered into a monopheletic group closely related
to the dwarf shrub-like interspecific progeny ‘Prob’ (33), the Nei’s genetic distance
ranging from 0.1040 to 0.1349, supports the above classic taxonomy. P. maximowiczii
(31) further formed a group with the species P. humilis (34), P. tomentosa (35) and
the progeny ‘Prob’. All three wild species mentioned (31, 34, and 35) are native to
China and are closely related in the phylogenetic tree, having a relatively high genetic
identity. They also clustered with the wild species P. mahaleb (24) originating in
Hungary, and the Japanese species P. serrulata var. lannesiana (32). Ingram (1948)
placed P. maximowiczii (31) and P. mahaleb (24) in the phyllomahaleb section of the
Prunus subgenus cerasus. P. mahaleb (24) showed greater proximity to the wild
species P. maximowiczii (31) in the phylogenetic tree and could be separated from
the species listed as nos31, 34, 33 and 35 (65% significance).
‘Colt’ (29) is the interspecific hybrid of P. avium and P. pseudocerasus, which
would account for its relationship with P. avium and P. pseudocerasus. This is
consistent with the previous studies on cherry species by using an isozyme technique
(Granger et al. 1993).
P. cerasus (25-28) clustered into a group with P. pseudocerasus, and then
significantly correlated with P. avium (100% significance). It is believed that
P. cerasus originated as a hybrid between P. avium and P. fruticosa. In terms of
geographical origin, P. avium is indigenous to the southwest part of Asia and Europe
and is thought to have originated in the region of the Caspian and Black Seas, from
where it slowly spread, while P. pseudocerasus has its origin in Southwest China and
the area of the Yangtze River. Despite the difference in geographical origin, the cluster
analysis has revealed that P. pseudocerasus and P. avium formed a distinct cluster in
the phylogenetic tree. This close relationship (GImax=0.9396) indicates phylogenetically
that, besides the geographical origin (Luo et al., 2001), genotypes in the species may
also account for the interspecific phylogenetic relationship. On the other hand, in
terms of chromosomal ploidy, P. tomentosa, P. mahaleb and P. serrulata var.
lannesiana are diploid, P. cerasus (an interspecific hybrid of P. avium and P. fruticosa)
and P. pseudocerasus are tetraploids, while P. avium includes diploids, triploids and
tetraploids (Webster et al., 1996; Yu, 1986). The consistency between the ploidy and
313
the phylogenetic tree’s topology further showed a relatively close genetic relationship
between P. pseudocerasus and P. avium, which complies with the studies by Malusa
(1996). The above results indicated that the phylogenetic relationships among Prunus
species revealed by the phylogenetic tree are consistent with the well-established
basic taxonomical frame (Ingram, 1948; Rehder, 1974). The adoption of PCR amplified
DNA fragments is a powerful tool for the analysis of genetic variation of Prunus
germplasm, and can reveal the interspecific phylogenetic relationships at the molecular
level.
Acknowledgements We thank to Dr. J. D. Quinlan and Dr. Karoly Hrotko for
giving us advices. This research was supported by the China Science and Technology
Commission program CHN3319. The experiments comply with the current laws of
the country in which the experiments were carried out.
Gauta
2006 07 24
Parengta spausdinti
2006 08 09
References
1. B o r i t z k i M, P l i e s k e J, S t r u s s D. (2000) Cultivar identification in
sweet cherry using AFLP and microsatellite markers. Acta Hort 538:505–510.
2. F e l s e n s t e i n J. (1985) Confidence limits on phylogenies: An approach
using the bootstrap. Evolution 39:783–791.
3. G e r l a c h H K, S t o s s e r R. (1998) Sweet cherry cultivar identification
using RAPD derived DNA fingerprints. Acta Hort 468:63–69.
4. G r a n g e r A R , C l a r k e G R , J a c k s o n J F . (1993) Sweet cherry
cultivar identification by leaf isozyme polymorphism. Theor Appl Genet 86:458–464.
5. H o r m a z a J I. (1999) Early selection in cherry combining RAPDs with embryo
culture. Scientia Horticulturae 79:121–126.
6. H u a n g H, L a y n e D R, K u b i s i a k T L. (2003) Molecular
characterization of cultivated pawpaw (Asimina triloba) using RAPD markers. J. Amer.
Soc. Hort. Sci 128(1):85–93.
7. I n g r a m C. (1948) Ornamental Cherries. Country life, London.
8. J o r d a n o P, G o d o y J A. (2000) RAPD variation and population genetic
structure in Prunus mahaleb, an animal-dispersed tree. Molecular Ecology 9:1293-1305.
9. L u o S L, H e P C, Z h e n g X Q, Z h o u P. (2001) Genetic diversity in
wild grapes native to China based on RAPD analysis. Acta Botanica Sinica 43(2):158–163.
10. M a l u s a E, M a r c h e s i n i A. (1996) Use of DNA amplified sequences
for the genetic analysis of Prunus. Atti Soc. it. Sci. nat. Museo civ. Stor. nat. Milano
135(2):430–436.
11. N e i M. (1978) Estimation of average heterozygosity and genetic distance from
a small number of individuals. Genetics 89:583–590.
12. N e i M, K u m a r S. (2000) Phylogenetic Inference: Maximum Parsimony
Methods. Molecular evolution and phylogenetics. Oxford University Press, New York,
pp. 115–146.
13. R e h d e r A. (1974) Cultivated trees and shrubs hardy in north America, 2nd
edn. Macmillan, New York.
314
14. S t o c k i n g e r E J, M u l i n i x C A, L o n g C M, B r e t t i n T S,
I e z z o n i A F. (1996) A linkage map of sweet cherry based on RAPD analysis of a
microspore-derived callus culture population. J Hered 87:214–218.
15. W a n g X P, W a n g Y J, Z h o u P, Z h e n g X Q. (2002) RAPD
analysis in F1 progeny from a grape interspecific crossing. Jour. of Northwest Sci-Tech
Univ. of Agri. and For. (Nat. Sci. Ed.) 30(6):81–84.
16. W e b s t e r A D, L o o n e y N E. (1996) CHERRIES: Crop Physiology,
Production and Users. CAB INTERNATIONAL, Wallingford.
17. W i l l i a m s J G K, K u b e l i k A R, L i v a k K J, R a f a l s k i J A,
T i n g e y V. (1990) DNA polymorphisms amplified by arbitrary primers are useful as
genetic markers. Nucleic Acids Res., 18:6531–6535.
18. Y u D J. (1986) Cerasus Mill. Flora of China 38:46-87. Science Press, Beijing.
19. Z h o u L, K a p p e l P A, W i e r s m a P A, H a m p s o n C,
B a k k e r e n G. (2002) Genetic analysis and discrimination of sweet cherry cultivars
using amplified fragment length polymorphism fingerprints. J Amer Soc Hort Sci 127:786–792.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
302–315.
LAUKINIØ VYÐNIØ GENETINËS VARIACIJOS TYRIMAI PANAUDOJANT
RAPD ANALIZÆ
Yu-Liang Cai, Gui-Fang Zhao, Dong-Wei Cao
Santrauka
Tirta 8 vyðniø rûðiø ir 2 tarprûðiniø hibridø atsitiktinai amplifikuotø polimorfiniø DNR
sekø variacija. 48 ið 130 pasirinktinai oligonukleotidiniai þymenys tirti PGR padauginti,
siekiant generuoti polimorfizmus. Filogenetinë analizë atlikta dviem distancinës matricos
metodais. Siekiant atskleisti rûðiø ir veisliø santykius, buvo sukurta dendograma. Rezultatai
parodë, kad ið viso buvo 840 padaugintø lokusø; 23 treðniø ir 4 vyðniø veislës buvo
sugrupuotos su atitinkamai 569 ir 247 polimorfiniais lokusais, o tai atitinkamai 67,74 ir
29,40% visos variacijos. P. tomentosa T., P. fruticosa var. aucta P. ir P. humilis B. sudarë
monofiletinæ grupæ. Buvo stebëtas santykis tarp P. pseudocerasus L. ir ‘Colt’, kurios
sudarë kità artimai susijusià grupæ, o P. avium L., P. cerasus L. ir kitos vyðniø rûðys labiau
skyrësi. Genetiðkai skirtingø Prunus rûðiø genetinis skirtingumas siekë nuo 0,0623 iki
0,2719. Vaismedþio topologija ið esmës atitiko taksonominæ klasifikacijà. Rezultatai parodë,
kad, iðskyrus treðniø veislæ ’Hongdeng‘, buvo vienas ar daugiau vyðniø rûðims ir veislëms
bûdingø RAPD þymenø. Panaudojant ðiuos specifinius þymenis, gali bûti nustatomas
vyðniø rûðiø ir veisliø tapatumas, todël egzistuoja galimybë anksti parinkti geras hibridø
savybes.
Reikðminiai þodþiai: vyðnios, RAPD, rûðys, genetiniai santykiai.
315
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 316–321.
SIMPLE IDENTIFICATION OF SWEET CHERRY
ROOTSTOCKS PHL USING RAPD MARKERS
Anna LISEK, Maùgorzata KORBIN, Elýbieta ROZPARA
Research Institute of Pomology and Floriculture, Skierniewice,
Pomologiczna 18, Poland.
E-mail: [email protected], [email protected], [email protected]
The studies were conducted on plants of three sweet cherry rootstocks P-HL A,
P-HL B and P-HL C kept in germplasm collections of the Institute of Pomology and
Floriculture in Skierniewice. DNA polymorphism was analysed by RAPD-PCR technique.
DNA was amplified with 59 out of 70 tested primers (Operon Technologies, Inc.). Totally,
59 informative products (19% of total band number) with length between 500 bp and
1830 bp were amplified with 28 primers. Ten primers generated especially high polymorphism
and each of them allowed to diversify analysed rootstocks. DNA patterns for each rootstock
were established. Obtained results confirm the suitability of RAPD-PCR technique for
diversification of sweet cherry rootstocks.
Key words: DNA polymorphism, fingerprinting, molecular markers, Prunus avium L.
Introduction. Intensive sweet cherry cultivation needs weak-growing
rootstocks. Study on dwarf rootstocks usefulness for intensive orchards have been
carried out at the Research Institute of Pomology and Floriculture for many years.
P-HLs selected in Czech Republic within Prunus avium L. (Wertheim, 1998) are
known as rootstocks significantly reducing tree vigour and increasing yield (Grzyb
et al., 1998). According to previous experiments rootstock P-HL A accelerate the
ripening time of fruits and favourably influence the quality of fruits (Rozpara et al.,
2004). Data collected by other authors showed big differences in growth and vigour
of trees grafted on different types of rootstocks PHL. Precise identification of each
rootstock with molecular markers allows avoiding these problems. Markers generated
on the base of DNA polymorphism analysis make possible the identification of
genotypes also for plant material characterizing with high similarity of morphological
traits. Many authors presented high efficiency of RAPD-technique for diversification
of Prunus cultivars: peach (Zhen-Xiang et al., 1996), plum (Ortiz et al., 1997; Shimada
et al., 1999) and almond (Bartolozzi et al., 1998; Martins et al., 2003). For identification
of sweet cherry cultivars RAPD, SSR and AFLP techniques were used (Gerlach,
Stosser, 1998; Boritzki et al., 2000; Zhou et al., 2002; Dirlewanger et al., 2002; Lisek
et al., 2005).
316
In this work, DNA polymorphism of sweet cherry rootstock P-HL with RAPD
technique was analysed. DNA patterns for each genotype were established for further
identification of rootstock PHL types.
Materials and methods. P l a n t m a t e r i a l a n d D N A
i s o l a t i o n. Three sweet cherry rootstocks P-HL A, P-HL B and P-HL C were
obtained from the field collection of Research Institute of Pomology and Floriculture
in Skierniewice. Genomic DNA was extracted from shoot tips with young leaves
(2 g per each sample) with CTAB-based method (Doyle, Doyle, 1990). Nucleic acid
concentration was measured spectrophotometrically (at 260 nm). DNA was diluted
to 10 ng per 1 µl for further analysis.
R A P D - P C R a n a l y s i s. Amplification was carried out in a volume of
13 ml containing 10 x PCR buffer, 2.5 mM of MgCl2, 0.1 mM of each nucleotide,
0.325 U of Taq polymerase, 0.35 mM of primer and 13 ng of template (DNA).
Totally 70 primers (Operon Technologies Inc.) from groups OPB, OPG, OPT and
OPU were tested. DNA amplifications were performed in MJ Research Thermocycler
(40 cycles: 95oC/30 s, 40oC/45 s, 72oC/90 s). PCR products were separated in 1,2 %
agarose gels, stained with ethidium bromide and visualized under UV light. Only
clearly distinct and reproducible bands were selected for the further analysis.
Results and discussion. DNA amplification was observed in reactions with 59
out of 70 used primers, which generated altogether 310 fragments. Polymorphic
products were obtained in reactions with 28 primers. Totally fifty-nine RAPD markers
were identified, defined as 19% of the total band number. The size of polymorphic
fragments ranged between 500 bp and 1830 bp. The highest number of the RAPD
polymorphic fragments was observed in reactions with the primers OPG 16
(5 products) and OPU 15 (4 products). Each of primers: OPB 08, OPG 08, OPG 11,
OPT 01, OPT 04, OPT 06, OPU 19 and OPU 20 generated three polymorphic
fragments.
Similar results concerning polymorphism generation with RAPD were obtained
for different Prunus species. For example, three to six primers allowed to identify 31
plum cultivars and 18 peach cultivars, respectively (Ortiz et al., 1997; Zhen-Xiang et
al., 1996). Six selected RAPD primers allowed to obtain 63 fragments diversifying
40 almond cultivars (Martins et al., 2003). Diversification of 19 sweet cherry cultivars
was possible using six RAPD primers (Lisek et al., 2005). Generally, 104 RAPD
markers necessary to diversify 40 genotypes from subspecies Lithocerasus were
obtained in reaction with 53 primers (Shimada et al., 2001).
Simultaneously, the RAPD technique revealed 39,4% polymorphism for peach
and 85,4% for Japanese plum (Warburton, Bliss, 1996; Bellini et al., 1998). Low
level of polymorphism in our study (19%) can be caused by small size of genome of
sweet cherry (0,7 pg) (Arumuganathan, Earle, 1991). Similar result has been obtained
by other authors, e.g. 19% of polymorphism was observed with AFLP technique
(Zhou et al., 2002), 17-21% with SSR markers (Boritzki et al., 2000; Struss et al.,
2003) and 14,6% with RAPD technique (Lisek et al., 2005). The low level of DNA
polymorhism can be also a reason of difficulties in diversification of some sweet
cherry cultivars with RAPD markers (Gerlach, Stosser, 1998). In our study ten
primers generated especially high polymorphism and each of them allowed to diversify
317
analysed rootstocks (Table 1). All these primers were used to prepare DNA patterns
characterizing each rootstock (Fig. 1).
T a b l e. DNA polymorphism in RAPD-PCR on the template of
genomic DNA of 3 sweet cherry rootstocks PHL
(1 – presence, 0 – lack of polymorphic products)
L e n t e l ë. Treðniø trijø PHL poskiepiø DNR polimorfizmas (1 – yra,
0 – polimorfiniø produktø trûksta)
Rootstock / Poskiepis
Primer
Length of polymorphic fragment
Pradmuo
Polimorfinio fragmento ilgis (bp)
PHL A
PHL B
PHL C
1730
0
1
0
1320
0
1
1
1400
0
1
1
870
1
0
1
1350
0
1
1
990
0
1
1
OPB 06
OPG 06
OPG 08
OPT 04
OPT 06
OPT 07
OPT 18
OPU 05
OPU 14
OPU 15
800
1
0
1
1510
0
1
1
1200
0
1
0
1030
1
1
0
600
1
0
1
560
0
1
1
560
1
0
0
770
0
1
1
560
1
1
0
1010
1
0
1
860
0
1
1
930
1
1
0
850
1
0
1
1100
0
0
1
1040
0
1
0
1520
1
0
0
1460
0
0
1
1360
0
1
0
1080
0
1
0
318
F i g.
DNA patterns of 3 sweet
cherry rootstock: lines 1,2,3 – PHL A,
lines 4,5,6 – PHL B, lines 7,8,9 – PHL C.
Applied primers: OPG 16 – lines 1, 4, 7,
OPT 07 – lines 2, 5, 8, and OPU 15 –
lines 3, 6, 9. M - Eco RI and HindIII
digested ë–DNA marker
P a v. Trijø treðniø poskiepiø DNR
pavyzdþiai: 1,2,3 linijos – PHL A, 4,5,6
linijos – PHL B, 7,8,9 linijos – PHL C.
Naudoti þymenys: OPG 16 – 1, 4, 7 linijos,
OPT 07 – 2, 5, 8 linijos ir OPU 15 – 3, 6, 9
linijos. M – Eco RI ir HindIII suskaidytas
ë–DNR þymuo
Conclusions. 1. The obtained results confirm the suitability of RAPD-PCR
technique for identifying of sweet cherry rootstocks.
2. Even a low level of DNA polymorphism was enough to distinguish between
tested rootstocks.
Gauta
2006 05 23
Parengta spausdinti
2006 08 08
References
1. A r u m u g a n a t h a n K., E a r l e E. D. Nuclear DNA content of some
important plant species // Plant Mol. Biol. Rep. 1991. Vol. 9: 208–218.
2. B a r t o l o z z i F., W a r b u r t o n M. L., A r u l s e k a r S.,
G r a d z i e l T. M. Genetic characterization and relatedness among California almond
cultivars and breeding lines detected by randomly amplified polymorphic DNA (RAPD)
analysis // J. Amer. Soc. Hort. Sci. 1998. Vol. 123: 381–387.
3. B e l l i n i E., G i o r d a n i E., N e n c e t t i V., P a f f e t t i D. Genetic
relationships in Japanese plum cultivars by molecular markers // Acta horticulturae. 1998.
Vol. 478: 53—59.
4. B o r i t z k i M., P l i e s k e J., S t r u s s D. Cultivar identification in
sweet cherry (Prunus avium L.) using AFLP microsatellite markers // Acta horticulturae.
2000. Vol. 538: 505–510.
319
5. D i r l e w a n g e r E., C o s s o n P., T a v a u d M., A r a n z a n a
M. J., P o i z a t C., Z a n e t t o A., A r u s P., L a i g r e t F. Development of
microsatellite markers in peach [Prunus persica (L.) Batsch] and their use in genetic
diversity analysis in peach and sweet cherry (Prunus avium L.) // Theor Appl Genet. 2002.
Vol. 105: 127–138.
6. D o y l e J. J. and D o y l e J. L. Isolation of plant DNA from fresh tissue //
Focus. 1990. Vol. 12:13–15.
7. G e r l a c h H. K., S t o s s e r R. Sweet cherry cultivar identification using
RAPD-derived DNA fingerprints // Acta horticulturae. 1998. Vol. 468: 63–69.
8. G r z y b Z. S., S i t a r e k M., O m i e c i ñ s k a B. Growth and fruiting
of five sweet cherry cultivars on dwarfing and vigorous rootstocks // Acta horticulturae.
1998. Vol. 468: 333–338.
9. L i s e k A., K o r b i n M., R o z p a r a E. Differentiation of sweet cherry
(Prunus avium L.) cultivars with simply genetated RAPD markers // J. Fruit Ornam. Plant
Res. 2005. Vol. 13 (Special ed.): 53–59.
10. M a r t i n s M., T e n r e i r o R., O l i v e i r a M. M. Genetic relatedness
of Portugese almond cultivars assessed by RAPD and ISSR markers // Plant Cell Rep.
2003. Vol. 22: 71–78.
11. O r t i z A., R e n a u d R., C a l z a d a I., R i t t e r E. Analysis of
plum cultivars with RAPD markers // J. Hort. Sci. 1997. Vol. 72: 1–9.
12. R o z p a r a E., G r z y b Z. S., O m i e c i ñ s k a B., C z y n c z y k A.
Results of eight years of research on the growth and yield of three sweet cherry cultivars
grafted on ‘PHL A’ rootstock // Acta horticulturae. 2004. Vol. 663: 965–967.
13. S h i m a d a T., H a y a m a H., H a j i T., Y a m a g u c h i M.,
Y o s h i d a M. Genetic diversity of plums characterized by random amplified
polymorphic DNA (RAPD) analysis // Euphytica. 1999. Vol. 109: 143–147.
14. S h i m a d a T., H a y a m a H., N i s h i m u r a K., Y a m a g u c h i
M., Y o s h i d a M. The genetic diversties of 4 species of subg. Lithocerasus (Prunus,
Rosaceae) revealed by RAPD analysis // Euphytica. 2001. Vol. 117: 85–90.
15. S t r u s s D., A h m a d R., S o u t h w i c k S. M. Analysis of sweet
cherry (Prunus avium L.) cultivars using SSR and AFLP markers // J. Amer. Soc. Hort. Sci.
2003. Vol. 128: 904–909.
16. W a r b u r t o n M. L., B l i s s A. Genetic diversity in peach (Prunus
persica L. Batch.) revealed by randomly amplified polymorphic DNA (RAPD) markers and
compared to inbreeding coefficients // J. Amer. Soc. Hort. Sci. 1996. Vol. 121: 1012–1019.
17. W e r t h e i m S. J. Rootstock guide. Wilhelminadorp, 1998. 108
18. Z h e n - X i a n g L., R e i g h a r d G. L., B a i r d W. V., A b b o t t
A . G., R a j a p a k s e S. Identification of peach rootstock cultivars by RAPD markers
// Hortscience. 1996. Vol. 31: 127–129.
19. Z h o u L., K a p p e l F., H a m p s o n C., W i e r s m a P. A.,
B a k k e r e n G. Genetic analysis and discrimination of sweet cherry cultivars and
selections using amplified fragment length polymorphism fingerprints // J. Amer. Soc.
Hort. Sci. 2002. Vol. 127: 786–792.
320
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
316–321.
PAPRASTAS TREÐNIØ PHL POSKIEPIØ IDENTIFIKAVIMAS
PANAUDOJANT RAPD ÞYMENIS
A. Lisek, M. Korbin, E. Rozpara
Santrauka
Atlikti trijø treðniø poskiepiø (P-HL A, P-HL B ir P-HL C) sodinukø, augintø Pomologijos
ir gëlininkystës instituto Skierniewice germplazmos kolekcijose, tyrimai. DNR polimorfizmas
analizuotas panaudojant RAPD-PCR technikà. DNR buvo pagausinta 59 ið 70 tirtø
pradmenø (Operon Technologies, Inc.). Ið viso 59 informatyvûs produktai (19% bendro
grupës skaièiaus), kuriø ilgis – nuo 500 iki 1830 bp, buvo pagausinti 28 pradmenimis.
Deðimt pradmenø generavo itin aukðtà polimorfizmà ir kiekvienas ið jø suteikë galimybæ
ávairinti analizuojamus poskiepius. Buvo nustatytos kiekvieno poskiepio DNR struktûros.
Gauti rezultatai patvirtina, kad RAPD-PCR technika yra tinkama treðniø poskiepiams ávairinti.
Reikðminiai þodþiai: DNA polimorfizmas, atspaudø metodas, molekuliniai þymekliai,
Prunus avium L.
321
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 322–326.
COMPARISON OF CYDONIA AND PYRUS ROOTSTOCKS
IN ESTONIA, LATVIA AND LITHUANIA
Edgar HAAK1, Darius KVIKLYS2, Janis LEPSIS3
Polli Horticultural Research Centre of the Institute of Agricultural and
Environmental Sciences of the Estonian University of Life Sciences,
Karksi-Nuia 69104, Estonia. E-mail: [email protected].
Lithuanian Institute of Horticulture, Kauno 30, LT–54333 Babtai,
Kaunas distr., Lithuania. E-mail: [email protected].
Pure Horticultural Research Station, Tukuma distr. LV–3124, Latvia.
E-mail: [email protected]
The co-operative experiment “Baltic fruit rootstock” was established in three Baltic
states – Estonia (at Polli), Latvia (at Pure) and Lithuania (at Babtai) in 2001. The cultivar
‘Suvenirs’ was grafted on three Cydonia rootstocks: BA29, QA and QC (the latter was
missing in Estonia), and four Pyrus rootstocks: vegetative Pyrodwarf and OHF 333 and
seedlings Kirchensaller Mostbirne, and Kazrausu. In Lithuania (at Babtai) the trunks on
every rootstock were thicker than in two other localities. The trees on the clones QC were
founded to be smaller and the trees on Pyrodwarf, OHF 333 and Kirchensaller Mostbirne
were significantly more vigorous than these on the standard clone BA29. In Latvia (at
Pure), the trees on all Pyrus rootstocks were more vigorous than these on Cydonia
rootstocs. In Estonia (at Polli), the trees on Pyrodwarf and OHF 333 were found to be
weaker than these on Cydonia rootstocks. The first crop in Lithuania appeared in the
fourth year after planting only on Cydonia and Pyrodwarf rootstocks. In Estonia and
Latvia, the first crop appeared in the fifth year on all rootstocks due to the entire killing of
flowers in the fourth year by spring night frosts; the first crop was bigger on Cydonia
rootstocks. In Lithuania, the fruit mass was bigger on OHF 333 than that on BA 29. Young
pear trees of the cultivar ‘Suvenirs’ are less vigorous on Cydonia rootstocks. However, in
some localities the trees on Pyrus rootstocks Pyrodwarf and OHF 333 may be even weaker
then these on Cydonia rootstocks.
Key words: pear, rootstock, Baltic states.
Introduction. Commercial pear growing in Estonia, Latvia and Lithuania is not
very perspective, due to severe winter damages. However, pear trees are growing in
many home gardens on seedling rootstock Pyrus pyraster. The trees on vigorous
rootstocks start to bear fruit late and take place.
It is possible to grow the trees on less vigorous rootstocks. Previous rootstock
trials have included Cydonia A and C rootstocks, but in the colder winter-conditions
322
many trees perished. The most damaged were the trees on Cydonia QC rootstock
even at West European climate conditions (Weber, 2001). In Latvia (Lepsis et al.,
2004) and Estonia even Cydonia QA rootstock was not winter hardy (Palk, 1987).
In Lithuania QA, S 1 and K11 showed promising results (Kviklys, 2005; Kviklys,
Kviklienë, 2004), nevertheless Pyrus clonal rootstocks must be evaluated.
In 1998, the Baltic fruit rootstock study was initiated in three Baltic States (Bite
et al., 1999) and first results reported (Bite et al., 2004).
The aim of the trial was to evaluate pear rootstocks performance in different
geographical localities.
Material and methods. The planting material was propagated at the Pure
Experimental station. The trees were planted at three sites in the spring of 2001: at
the Lithuanian Institute of Horticulture – Babtai, at the Pure Experimental Station in
Latvia, and at the Polli Ressearch Centre of the Institute of Agricultural and
Environmental Sciences of the Estonian University of Life Sciences. The geographical
locations are: Babtai in Lithuania 55° 60’ N, 23° 48’ E, Pure in Latvia 57° 02’N, 22°
52’E, and Polli in Estonia 58° 67’N, 25° 33’E.
Pear cv. ‘Suvenirs’was propagated on following rootstocks: Cydonia BA29,
Cydonia QA, Cydonia QC, not planted in Estonia, Pyrus Pyrodwarf, Pyrus OHF333,
Pyrus Kirchensaller Mostbirne seedlings, and Pyrus Kazrausu seedlings. An interstem
Staras No. 31 was used for trees on Cydonia rootstocks to surpass the incompatibility
between scion and rootstock. In Lithuania the soil humus content was 2.5%,
P2O5 – 255 mg per kg, K2O – 230 mg per kg, in Latvia the soil humus content was
1.8%, P2O5 –189 mg per kg, K2O – 151 mg per kg. In Estonia the experiment was
located on a medium sod-podzolic soil. The tree spacing in Estonian experiment was
4.0 x 1.5 m, in Latvia and Lithuania there was a choice: for clonal rootstocks –
4 x 2 m and for seedling rootstock – 4 x 3 m. The space between the rows was held
as grassland, and the row-stripe was managed by herbicides.
Cydonia BA29 was standard rootstock for comparison. There were 4 replications
in every variant, 3 trees per plot. Trunk diameter of each tree was measured every
autumn at the height of 30 cm and trunk cross-sectional area (TCSA) was calculated
in 2005. Tree height and canopy diameter were measured only in Estonia. Fruits
were harvested in 2004 (in Lithuania only) and in 2005 and yield (kg/tree) was
recorded. The average fruit weight was calculated only in Lithuania. Statistical analyses
of data were performed (p d” 0.05).
The weather conditions in Estonia and Lithuania didn’t differ substantially during
the years 2001–2005. Only the amount of precipitations was different: at Polli (Estonia)
the summer of 2002 was dryer.
Results and discussion. TCSA in Lithuania (all variants) was substantially
bigger than in Estonia and Latvia (Table), due to more fertile soil. In Lithuania the
trees on Cydonia QC were substantially slender than on Cydonia BA29, Pyrus
Pyrodwarf, and Mostbirne. In Latvia the trees on Cydonia rootstocks didn’t differ
in TCSA. However, the trees on all Pyrus rootstocks were much more thicker than
on Cydonia rootstocks. In Estonian-experiment, the trees only on Pyrus Pyrodwarf
and Pyrus OHF 333 were slender and the crown volume was smaller than these of all
Cydonia rootstocks and Mostbirne, and Kazrausu.
323
T a b l e. Trunk cross-sectional area (TCSA) after five growing
seasons, yield per tree, mean fruit weight, height of trees
and crown volume
L e n t e l ë. Kamieno skerspjûvio plotas (KSP) po penkiø augimo sezonø,
vaismedþio derlius, vidutinë vaisiaus masë, vaismedþiø aukðtis ir
vainiko tûris
Lithuania / Lietuva
Rootstock
Poskiepis
BA29
QC
QA
Pyrodwarf
OHF-333
Mostbirne
Kazrausu
LSD 0.5
Mean
fruit
weight
TCS
A
KSP,
cm2
Derlius,
kg/vaism.
Vidutinë
vaisiaus
masë, g
32.2
23.7*
30.2
38.5*
40.7*
43.0*
35.2
16.5
11.5*
13.3
11.4*
11.0*
9.2*
8.7*
3.7
3.9
Yield,
kg/tree
Latvia / Latvija
Estonia / Estija
Yield,
kg/tree
TCSA
2
KSP, cm
TCSA
KSP,
cm2
Derlius,
kg/vaism.
159
158
163
164
175*
154
151
16.6
15.2
16.6
27.7*
22.9*
34.2*
38.5*
23.9
24.6
18.7*
15.8*
23.9
20.7
13.6
2.0
1.8
Height
Aukštis,
Crown
volume
m
Vainiko
3
tûris, m
15.5
16.8
1.7*
3.8*
4.6*
5.5*
3.5
3.4
3.4
3.3
3.4
3.5
5.5
5.1
4.0*
3.9*
5.3
4.8
3.2
0.2
0.7
The differences in trunk diameter were found, especially in Lithuania and Estonia,
during the first three years after planting; in the forth and fifth years the yearly
increase was stable, without differences. In Latvia, the differences were formed in
the fourth and fifth years (Fig.); this was mainly stated in the trees on Mostbirne and
Kazrausu rootstocks.
F i g. Pear tree trunk diameter in 2003 and increase of diameter in 2004 and 2005
P a v. Kriauðiø kamieno skersmuo 2003 m. ir skersmens padidëjimas 2004 ir 2005 m.
324
The beginning of yield in Lithuania on Cydonia rootstocks and on Pyrodwarf
was in fourth year. In Estonia, the spring night frosts killed all the flowers that year,
thus the first fruits appeared a year later. In fifth year, the trees on Cydonia BA29 and
QA rootstocks, both in Lithuania and Estonia, were more productive than on the
other rootstocks (Table). The trees on BA29 surpassed the trees on Pyrus rootstocks
by 50–70% in Lithuania and 65–90% in Estonia. The smallest yield at Polli was
reported for Pyrodwarf rootstock.
Average fruit weight was reported only for Lithuania: it was substantially greater
on the OHF 333 rootstock if to compare with Cydonia BA29.
Data in the literature stated that trees on Cydonia BA29 are the most vigorous
among Cydonia rootstocks (Carrero, Ortiz, 1984; Weber, 2001). However, there are
information that both may be the same size (Loreti et al., 2002). The latter coincide
with the results in Lithuania, Latvia and Estonia. The Pyrus Pyrodwarf rootstock
produces by the evaluation of the breeder (Jacob, 1998) small trees, almost similar
to Cydonia QA. The rootstock Pyrus OHF 333 appeared too vigorous (Weber, 2001).
In Switzerland, the trees on OHF 333 were influenced by scion but were 20-60%
more vigorous than the trees on Cydonia QA (Money and Evequos, 1999).
Conclusions. The rootstocks tended to have different influence on tree size,
depending on growing site.
In our experiment, the trees on Pyrus rootstocks in Lithuania and Latvia were
more vigorous, but in Estonia produced smaller trees than on Cydonia BA29. The
trees on Kirchensaller Mostbirne and Kazrausu varied greatly from one site to another.
In Latvia and Estonia they were more vigorous than on Pyrus Pyrodwarf and Pyrus
OHF 333, whereas in Lithuania there was no significant difference, presumably due
to more fertile soil.
Gauta
2006 06 08
Parengta spausdinti
2006 07 17
References
1. B i t e A., K v i k l y s D., U n i v e r T., L u k u t T. The beginning of
the project “Baltic fruit rootstock studies”. Acta Horticulturae. 2004. 658(1). P. 437–440.
2. B i t e A., K v i k l y s D., H a a k E., L u c u t T. F. International project
“Baltic Rootstock Studies”. Apple rootstocks for intensive orchards. Warszawa, 1999.
P. 17–18.
3. C a r r e r a M., O r t i z E. Performance of tree quince rootstocks for pears.
Acta Horticulturale. 1984. 161. P. 231–245.
4. J a c o b H. B. Pyrodwarf, a new clonal rootstock for high density pear orchards.
ISHS Acta Horticulturale 475. 1998. VII International Symposium on Pear Growing. P. 169–178.
5. K v i k l y s D. Poskiepiø átaka ‘Konferencinë’ kriauðiø vegetatyvinei ir
generatyvinei raidai // Sodininkystë ir darþininkystë, 24(2). 2005. P. 3–10.
6. K v i k l y s D., N. K v i k l i e n ë. Pear rootstock effect on growth,
productivity and fruit internal quality// Acta Horticulturae, 658(1). 2004. P. 359–364.
325
7. L e p s i s J., D r u d z e I., D e k e n s U. The evaluation of different plum
and pear rootstocks in the nursery. ISHS Acta Horticulturale. 658. 2004. P. 167–172.
8. L o r e t i F., M a s s a i R., F e i C., C i n e t t i F. Performance of
‘Conference’ cultivar on several quince and pear rootstocks: preliminary results. ISHS
Acta Horticulturale 596. 2002. P. 311–318.
9. M o n n e y F., E v e q o u s N. OHF und Quittenunterlagen für Birnen in
Vergleich. Schweiz, Z. Obst-Weinbau Nr. 26. 1999. P. 634–637.
10. P a l k J. Õuna- ja pirnipuude kasvatamine. Seemned, pookealused, istikud.
Tallin, Valgus, 1987. P. 102–105.
11. W e b e r H. J. Birnenunterlagen – keine M9 in Sicht. Obstbau in Rheinland
Platz. 2001. P. 1–9.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
322–326.
CYDONIA IR PYRUS POSKIEPIØ PALYGINIMAS ESTIJOJE, LATVIJOJE
IR LIETUVOJE
E. Haak, D. Kviklys, J. Lepsis
Santrauka
Vykdant Baltijos poskiepiø tyrimø programà, 2001 m. ‘Suvenirs’ kriauðiø veislës su
Cydonia poskiepiais BA29, QA ir QC (pastarojo Estijoje nebuvo) ir Pyrus poskiepiais:
vegetatyvinais – Pyrodwarf ir OHF 333 bei sëkliniais – Kirchensaller Mostbirne ir Kazrausu,
bandymai buvo árengti trijose Baltijos respublikose: Estijoje (Polli), Latvijoje (Pure) ir
Lietuvoje (Babtuose). Lietuvoje vaismedþiø kamienai su visais poskiepiais buvo storesni
negu kitose dviejose vietovëse. Vaismedþiai su QC vegetatyviniu poskiepiu buvo maþesni,
o su Pyrodwarf OHF 333 ir Kirchensaller Mostbirne – ið esmës augesni uþ vaismedþius
su standartiniu BA29 vegetatyviniu poskiepiu. Latvijoje vaismedþiai su visais Pyrus
poskiepiais buvo augesni uþ vaismedþius su Cydonia poskiepiais. Estijoje vaismedþiai su
Pyrodwarf ir OHF 333 buvo silpnesni uþ vaismedþius su Cydonia poskiepiais. Pirmàjá
derliø Lietuvoje ketvirtaisiais metais po pasodinimo davë tik vaismedþiai su Cydonia ir
Pyrodwarf poskiepiais. Estijoje ir Latvijoje pirmasis derlius skintas nuo vaismedþiø su
visais poskiepiais, bet tik penktaisiais metais, nes ketvirtaisiais metais po pasodinimo
pavasarinës ðalnos sunaikino visus þiedus. Pirmasis derlius buvo didesnis vaismedþiø su
Cydonia poskiepiais. Lietuvoje didesnë buvo vaismedþiø su OHF 333 vaisiaus masë negu
su BA 29. Jaunos ‘Suvenirs’ veislës kriauðës su Cydonia poskiepiais yra maþiau augios,
taèiau kai kuriose vietovëse vaismedþiai su Pyrus, Pyrodwarf ir OHF 333 gali bûti dar
silpnesni.
Reikðminiai þodþiai: kriauðës, poskiepiai, Baltijos respublikos.
326
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 327–333.
PERFORMANCE OF PRUNUS ROOTSTOCKS IN THE
2001 NC-140 PEACH TRIAL
G.L. REIGHARD1, T. BECKMAN, R. BELDING, B. BLACK,
J. CLINE, W. COWGILL, R. GODIN, M. KAPS, T. LINDSTROM,
D. OUELLETTE, L. STEIN, K. TAYLOR, C. WALSH,
M. WHITING and T. ROBINSON 2.
1
Clemson University, Department of Horticulture, Clemson, South Carolina,
29634-0319, USA. E-mail: [email protected]
Co-authors are NC-140 cooperators from Colorado, Georgia, Maryland,
Missouri, New Jersey, New York, South Carolina, Texas, Utah, Washington
and Ontario, Canada and are listed in Table 1.
2
Fourteen Prunus rootstock cultivars and selections budded with either ‘Redtop’,
‘Redhaven’ or ‘Cresthaven’ peach were planted at 10 locations in North America in 2001 in
a randomized block design with a tree spacing of 5 by 6 m and 8 replicates. This test
planting was a NC-140 Cooperative Regional Rootstock Project (www.nc140.org). There
were 14 rootstocks total, which included three peach seedling rootstocks: Lovell, Bailey,
and Guardian® BY520-9 [selection SC-17]. Clonal rootstocks included peach x almond
hybrids BH-4 and SLAP (Cornerstone); peach x plum hybrids K146-43 (Controller 5),
K146-44, and P30-135 (Controller 9); interspecific plum hybrids Hiawatha, Jaspi and Julior;
interspecific Prunus hybrids Cadaman® and VVA-1 (Krymsk® 1); and Prunus pumila
selection Pumiselect®. The largest trees were from Georgia, Maryland, and South Carolina.
BH-4, SLAP, SC-17, Lovell, and Cadaman® were the most vigorous rootstocks. Jaspi,
K146-43, K146-44 and VVA-1 were the least vigorous, having trunk circumferences
30-40% smaller than Lovell. No rootstock had a significantly higher survival rate than
Lovell at all locations. Julior, Jaspi, and VVA-1 had significantly more root suckers.
Cumulative fruit yields were highest on the peach seedling, peach x almond, and Cadaman®
rootstocks. Lowest cumulative yields were from trees on Jaspi, VVA-1, and K146-44
rootstocks. Fruit weight was significantly larger on BH-4, SLAP and Bailey rootstocks.
Bailey and Jaspi had the highest and lowest cumulative yield efficiency, respectively.
Keywords: peach x almond hybrids, peach x plum hybrids, Prunus persica L.
Introduction. Peach production in North America has relied on peach seedling
rootstocks since the mid-1800s. Entering the 21st century, peach growers must
confront replant problems, the loss of soil fumigants and agricultural chemicals,
increased production costs, and reduced yields due to shortened tree longevity. To
327
increase orchard productivity and efficiency, growers are looking for solutions via
new rootstocks that are more resistant to abiotic (winter cold damage, drought stress,
soil anaerobic conditions, etc.) and biotic stresses (root pathogens, soil nematodes,
bacterial and fungal cankers, etc.) as well as dwarfing (Layne, 1987; Reighard,
2002). The NC-140 project, a United States, Mexican and Canadian group of
cooperating researchers, was organized to test new rootstocks over a wide range of
sites in North America. Previous reports (Perry et al., 2000; Reighard, 2000; Reighard
et al., 2004) from this group have provided information on the performance of mostly
peach seedling rootstocks in multiple environments throughout the United States and
Canada.
In the past 5–10 years, clonal-propagated, interspecific Prunus rootstocks for
peach have been licensed and propagated by nurserymen in the United States. These
rootstocks had limited field-testing in North America, and thus were good candidates
for an NC-140 rootstock trial. To determine the horticultural merits of these rootstocks
under North American edaphic and climatic conditions, a NC-140 trial was initiated.
The objectives of this NC-140 trial were to evaluate these clonal peach rootstocks
for survival, tree vigor, yield, fruit quality, cold hardiness, nematode or disease tolerance
and replant performance in peach production regions.
Materials and methods. Authorization was obtained to test 12 proprietary
rootstocks and selections. Eleven of these were clonal rootstocks that included peach
x almond hybrids BH-4 and SLAP (Cornerstone); peach x plum hybrids
K146-43 (Controller 5), K146-44, and P30-135 (Controller 9); interspecific plum
hybrids Hiawatha, Jaspi and Julior; interspecific Prunus hybrids Cadaman® and
VVA-1 (Krymsk® 1); and Prunus pumila selection Pumiselect®. There were also
3 peach seedling rootstocks tested: Lovell and Bailey as controls and Guardian®
BY520-9 [selection SC-17]. Liners or seed of each virus-indexed rootstock were
collected in 1999 and sent to Burchell Nursery (Oakdale, California) for nursery
propagation and budding. Rootstocks were budded with virus-indexed ‘Cresthaven’,
‘Redhaven’ and ‘Redtop’ peach in 2000, and one cultivar budded on 12–14 rootstocks
was selected and shipped to each cooperator in January 2001 for planting in Spring
2001.
The trial’s experimental design consisted of 8 single-tree plots (=replicates) of
each rootstock planted in a randomized complete block design at all 10 locations in
the U.S. and Canada. Trees were spaced 5 m within rows and 6 m between rows.
Trees were headed at planting to a height of approximately 70–80 cm and trained to
an open center system. Supplemental irrigation was available and applied when
necessary. Application of pesticides, herbicides and fertilizer followed local
recommended practices for each state.
‘Cresthaven’ was planted in Colorado, Texas and Washington. ‘Redhaven’ was
planted in Missouri, New Jersey, Ontario and Utah. ‘Redtop’ was planted in Georgia,
Maryland and South Carolina. Data collected annually on each tree from each location
included survival, trunk circumference, root suckering, bloom date (90% flowers
open), fruit maturity date (10% fruit mature), fruit size (random 20-fruit sample),
tree yield, and yield efficiency. Not all rootstocks were available for all sites.
Cooperators and the test locations are listed in Table 1.
328
T a b l e 1. State cooperators, affiliations and locations of the 2001
NC-140 peach rootstock test.
1
l e n t e l ë.
State/Province
Valstija/provincija
2001 m. NC-140 persikø poskiepiø tyrimo bendradarbiai,
institucijos ir vietovës
Location
Vietovë
Colorado
Georgia
Grand Junction
Byron
Maryland
Missouri
New Jersey
Wye Mills
Mountain Grove
Bridgeton
New York
Ontario
South Carolina
(no planting)
Vineland
Clemson
Texas
Utah
Stonewall
Kaysville
Washington
Prosser
Cooperator
Bendradarbis
Ron Godin
Kathryn Taylor
Thomas Beckman
Christopher Walsh
Martin L. Kaps
Robert D. Belding
Winfred Cowgill, Jr.
Terence Robinson
John Cline
Gregory Reighard
David Ouellette
Larry Stein
Brent Black
Thor Lindstrom
Matthew Whiting
Affiliation
Institucija
Colorado State University
University of Georgia
USDA-ARS
University of Maryland
SW Missouri State University
Rutgers University
Rutgers University
Cornell University
University of Guelph
Clemson University
Clemson University
Texas A&M University
Utah State University
Utah State University
Washington State University
Due to unequal rootstock numbers among locations, data from 11 rootstocks
that were common to the 10 sites were analyzed by PROC MIXED (SAS, Cary, NC)
to detect rootstock differences for cultivar survival, trunk circumference, root
suckers, bloom date, maturity date, fruit weight, cumulative yield, and yield efficiency. In addition, data for each location were analyzed by PROC MIXED to determine
differences among the rootstocks present at that site. The SAS macro, PDMIX612,
was used to convert pair-wise differences between least squares means to letter
groupings using Fisher’s LSD. All data presented in Table 2 are least squares means
adjusted for missing cells.
Results. Table 2 shows data for 11 rootstocks that were common to all locations.
There were significant differences among rootstocks for the combined cultivars and
locations. In addition, there were significant rootstock and location interactions.
Tree survival (Table 2) differed significantly among rootstocks for different reasons.
No rootstock survived better than Lovell. Hiawatha had the poorest survival, and it
appeared that delayed incompatibility was occurring. Other rootstocks not planted
at all sites (data not shown = DNS) included Pumiselect®, which had very low
survival at 3 locations partly due to weak rooting or poor anchorage and VVA-1,
which had died from bacterial canker and/or incompatibility at 5 locations.
After 5 years, trunk circumference (i.e., radial growth) across all sites was
largest for trees on SC-17, Lovell, BH-4 and SLAP, whereas Jaspi, Julior, K146-43
and K146-44 produced the smallest trees (Table 2). The largest trees were from
Georgia, Maryland, and South Carolina, states that had longer growing seasons and
‘Redtop’ as the scion cultivar. Fruit weight and yields were correlated tree size. The
largest mean fruit weights were found on the peach/almond hybrid rootstocks, which
were also some of the largest trees. The smallest average fruit weights were from
329
cultivars on three of the four most dwarfing rootstocks; Jaspi, K146-43 and
K146-44. Cumulative yields were low for these dwarfing rootstocks, yet cumulative
yield efficiencies were not significantly different from the most vigorous rootstocks.
The highest yields were from the peach/almond hybrids and peach seedling rootstocks.
However, only Bailey had significantly higher yield efficiency than the dwarfing
rootstocks. In this trial, Bailey was the most yield efficient rootstock and Jaspi the
least efficient with all other rootstocks falling in between these two rootstocks.
T a b l e 2. Five-year combined performance of Redhaven,
Cresthaven, and Redtop on 11 rootstocks at 10 locations.
2
l e n t e l ë.
‘Redhaven’, ‘Cresthaven’ ir ‘Redtop’ veisliø persikø vaismedþiø su
11 poskiepiø vertinimas deðimtyje vietoviø penkerius tyrimo metus
Survival
Rootstock
Poskiepis
Vaismedþiø
išlikimasZ,
%
Trunk
circumference
Mean
fruit weight
Cumulative
fruit yield
Cumulative
yield
efficiency
Kamieno
skersmuo,
Vidutinë
vaisiaus masë,
cm
g
kg
2003–2005
2003–2005
2003–2005
Suminis
derlius,
Suminis
produktyvumas,
kg/cm2
Fall 2005
Fall 2005
2005 m. ruduo
2005 m. ruduo
BH-4
70.8 bc
36.9 ab
176 ab
64.9 ab
0.62 b
SLAP
71.2 bc
36.6 ab
180 a
66.6 ab
0.65 b
SC-17
72.5 bc
38.2 a
168 bcd
71.5 a
0.63 b
Bailey
89.7 abc
33.5 bc
173 abc
69.5 a
0.80 a
Julior
76.9 abc
28.8 def
168 bcd
40.6 cd
0.59 b
P30-135
94.4 a
30.3 cde
168 bcd
40.8 cd
0.56 bc
Jaspi
75.0 abc
25.4 f
155 f
26.7 d
0.46 c
Hiawatha
70.0 c
31.1 cd
165 cde
49.7 bc
0.62 b
K146-43
81.6 abc
26.9 ef
157 ef
34.9 cd
0.66 b
K146-44
91.2 ab
27.0 ef
160 def
30.3 d
0.56 bc
Lovell
87.0 abc
37.5 a
169 bcd
72.9 a
0.66 b
Locations in analysis
Tyrimo vietoviø skaièius
10
10
9
10
10
***
***
***
***
***
Rootstock x location
interaction
Poskiepio ir vietovës
s¹veika
Z
Mean separation within columns using Fisher's LSD, P< 0.05
Z
Vidutiniai skirtumai skiltyse pagal Fiðerio kriterijø, P< 0,05
*, **, ***
Significant at P< 0.05, 0.01, and 0.001, respectively.
*, **, *** Skirtumai esminiai, kai P atitinkamai <0,05, 0,01 ir 0,001.
330
Other data not given in Table 2 showed that Lovell, SC-17, SLAP, and BH-4
produced significantly larger (height and width) trees, and Jaspi and Julior had
significantly more root suckers than the other 9 rootstocks. Trees on Julior
consistently bloomed early and on K146-43 bloom was late. Fruit maturity was
significantly advanced only on Jaspi.
The rootstocks Cadaman®, Pumiselect®, and VVA-1, which were not planted
at all sites, had significant differences at the sites they were included (DNS).
Cadaman® was one of the most vigorous rootstocks with high yields, while VVA-1
was one of the least vigorous with low cumulative yields. VVA-1 also produced
many root suckers. Pumiselect® experienced significant windthrow at two locations
due to below ground root breakage below the graft union. Trees on Pumiselect®
also leaned (i.e., uneven anchorage) at some locations.
Discussion. Although no rootstock yielded better than Lovell, the cumulative
yield and yield efficiency data for the first 3 bearing years suggest that semi-dwarfing
and dwarfing rootstocks could be used in place of standard size rootstocks if tree
spacing is adjusted for the smaller canopies. However, some of the size-controlling
rootstocks tested exhibited incompatibility, horticultural, and/or disease problems
with peach scion cultivars, which likely limits their use as peach rootstocks since
these problems have been reported elsewhere (Reighard 2000; Loreti, Massai, 2002;
Massai, Loreti, 2004). Still the positive traits that these particular interspecific Prunus
rootstocks confer to peach cultivars such as growth control (Jacob, 1992; DeJong
et al., 2004), tolerance to waterlogging and calcareous soils (Reighard, 2002), and
resistance to soil fungi (Beckman, Pusey, 2001), nematodes (McFadden-Smith et
al., 1998; Nyczepir et al., 1999) and bacteria (Okie et al., 1994; Pinochet et al.,
2002) makes them a viable rootstock alternative to peach seedling rootstocks on
selected problem sites.
Conclusions. Significant differences among 14 rootstocks were found for all
characters measured, but no clonal rootstock in this trial yielded more than the three
peach seedling rootstocks on a per tree basis. Higher tree densities might show an
advantage for some dwarfing rootstocks, but this was not tested. Since most of the
locations were not difficult replant sites and the plantings are only 5 years old, trees
may not have yet been challenged by environmental stresses such as winter cold,
waterlogging, nematodes, soil fungi, or other factors. Therefore, it was not unexpected
that the peach seedling rootstocks performed equal or better than the other rootstocks
at low tree densities.
Acknowledgements. The authors would like to thank Burchell Nursery, Varieties
International, North American Plants, Hilltop Nursery, U.C. Davis and Clemson
University for either providing plant material or producing the trees, and the
International Dwarf Fruit Tree Association for financial support.
Gauta
2006 07 21
Parengta spausdinti
2006 08 09
331
References
1. B e c k m a n T. G., P u s e y P. L. 2001. Field testing peach rootstocks for
resistance to Armillaria root rot. HortScience 36 (1): 101–103.
2. D e J o n g T., J o h n s o n R. S., D o y l e J. F., W e i b e l A.,
S o l a r i L., B a s i l e B., M a r s a l J., R a m m i n g D., B r y l a D. 2004.
Growth, yield and physiological behaviour of size-controlling peach rootstocks developed
in California. Acta Horticulturae Vol. 658: 449–455.
3. J a c o b H. 1992. Prunus pumila L., eine geeignete schwachwachsende
Pfirsichuntererlage. Erwerbsobstbau 34: 144–146.
4. L a y n e R. E. C. 1987. Peach rootstocks. In: Rom R.C., Carlson R.F. (eds.)
Rootstocks for Fruit Crops. Wiley, New York. 185–216.
5. L o r e t i F., M a s s a i R. 2002. MiPAF targeted project for evaluation of
peach rootstocks in Italy: Results of six years of observations. Acta Horticulturae Vol.
592: 117–124.
6. M a s s a i R., L o r e t i F. 2004. Preliminary observations on nine peach
rootstocks grown in a replant soil. Acta Horticulturae Vol. 658: 185–192.
7. M c F a d d e n - S m i t h W., M i l e s N. W., P o t t e r J. W. 1998.
Greenhouse evaluation of Prunus rootstocks for resistance or tolerance to the rootlesion nematode (Pratylenchus penetrans). Acta Horticulturae Vol. 465: 723–730.
8. N y c z e p i r A. P., B e c k m a n T. G., R e i g h a r d G. L. 1999.
Reproduction and development of Meloidogyne sp. and M. javanica on Guardian peach
rootstock. Journal of Nematology 31 (3): 334–340.
9. O k i e W. R., B e c k m a n T. G., N y c z e p i r A. P., R e i g h a r d
G. L., N e w a l l J r. W. C., Z e h r E. I. 1994. BY520-9, A peach rootstock for the
southeastern United States that increases scion longevity. HortScience 29 (6): 705–706.
10. P e r r y R., R e i g h a r d G., F e r r e e D., B a r d e n J.,
B e c k m a n T., B r o w n G., C u m m i n s J., D u r n e r E., G r e e n e G.,
J o h n s o n J., L a y n e R., M o r r i s o n F., M y e r s S., O k i e W.,
R o m C., R o m R., T a y l o r B., W a l k e r D., W a r m u n d M., Y u K.
2000. Performance of the 1984 NC-140 Peach Rootstock Planting. J. Amer. Pom. Soc.
Vol. 54: 6–10.
11. P i n o c h e t J., F e r n a n d e z C., C u n i l l M., T o r r e n t s J.,
F e l i p e A., L o p e z M. M., L a s t r a B., P e n y a l v e r R. 2002. Response
of new interspecific hybrids for peach to root-knot and lesion nematodes, and crown gall.
Acta Horticulturae Vol. 592 (2): 707–716.
12. R e i g h a r d G. L. 2000. Peach rootstocks for the United States: are foreign
rootstocks the answer? HortTechnology Vol. 10: 714–718.
13. R e i g h a r d G. L. 2002. Current directions of peach rootstock programs
worldwide. Acta Horticulturae Vol. 592: 421–428.
14. R e i g h a r d G., A n d e r s e n R., A n d e r s o n J., A u t i o W.,
B e c k m a n T., B a k e r T., B e l d i n g R., B r o w n G., B y e r s P.,
C o w g i l l W., D e y t o n D., D u r n e r E., E r b A., F e r r e e D., G a u s
A., G o d i n R., H a y d e n R., H i r s t P., K a d i r S., K a p s M.,
L a r s e n H., L i n d s t r o m T., M i l e s N., M o r r i s o n F., M y e r s
S., O u e l l e t t e D., R o m C., S h a n e W., T a y l o r B., T a y l o r K.,
W a l s h C., W a r m u n d M. 2004. Growth and yield of Redhaven peach on 19
rootstocks at 20 North American locations. J. Amer. Pomol. Soc. Vol. 58(4): 174–202.
332
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
327–333.
PRUNUS POSKIEPIØ VERTINIMAS 2001 M. NC-140 PERSIKØ BANDYME
G.L. Reighard, T. Beckman, R. Belding, B. Black, J. Cline, W. Cowgill, R. Godin,
M. Kaps, T. Lindstrom, D. Ouellette, L. Stein, K. Taylor, C. Walsh, M. Whiting,
T. Robinson
Santrauka
2001 m. ‘Redtop’, ‘Redhaven’ arba ‘Cresthaven’ veisliø persikø vaismedþiai su
keturiolika Prunus poskiepiø ir selekciniø numeriø buvo pasodinti deðimtyje Ðiaurës
Amerikos vietoviø. Bandymas árengtas 8 atsitiktine tvarka parinktø blokø pakartojimais,
vaismedþiø sodinimo schema – 5 x 6 m. Tyrimas buvo NC-140 kooperacinio regioninio
poskiepiø projekto dalis (www.nc140.org). Tirti sëkliniai persikø poskiepiai Lovell, Bailey,
ir Guardian® BY520-9 (selekcinis Nr. SC-17), kloniniai poskiepiai BH-4 ir SLAP (Cornerstone)
(persiko ir migdolo hibridai), K146-43 (Controller 5), K146-44 ir P30-135 (Controller 9)
(persiko ir slyvos hibridai), Hiawatha, Jaspi ir Julior (tarprûðiniai slyvø hibridai), Cadaman®
ir VVA-1 (Krymsk® 1) (tarprûðiniai Prunus hibridai) bei Pumiselect® (Prunus pumila).
Augiausi vaismedþiai buvo Dþordþijoje, Merilende ir Pietø Karolinoje, augiausi
poskiepiai – BH-4, SLAP, SC-17, Lovell, ir Cadaman®. Maþiausiai augûs buvo Jaspi,
K146-43, K146-44 ir VVA-1 poskiepiai. Vaismedþiø su ðiais poskiepiais kamienø skersmuo
buvo 30–40% maþesnis negu su Lovell. Visose vietovëse daugiausia vaismedþiø iðgyveno
su Lovell poskiepiu. Julior, Jaspi ir VVA-1 poskiepiai iðaugino daugiausia ðaknø atþalø.
Didþiausià suminá derliø davë vaismedþiai su persikø sëjinukais, persiko ir migdolo hibridais
ir Cadaman®, maþiausià – su Jaspi, VVA-1 ir K146-44. Didþiausius vaisius iðaugino
vaismedþiai su BH-4, SLAP ir Bailey poskiepiais. Produktyviausi buvo vaismedþiai su
Bailey poskiepiu, maþiausiai produktyvûs – su Jaspi.
Reikðminiai þodþiai: persiko ir migdolo hibridai, persiko ir slyvos hibridai, Prunus
persica L.
333
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 334–341.
BALTIC FRUIT ROOTSTOCK STUDIES: EVALUATION OF
12 ROOTSTOCKS FOR APPLE CULTIVAR ‘AUKSIS’
Darius KVIKLYS, Nomeda KVIKLIENË
Lithuanian Institute of Horticulture LT-54333 Babtai, Kauno distr.,
Lithuania. E-mail: [email protected]
Andris BITE, Janis LEPSIS
Pure Horticultural Research Centre Pure, Tukuma distr., LV-3124, Latvia.
E-mail: [email protected]
Tamara LUKUT
Brest Agricultural Experimental Station Pruzhany, Brest distr., 225140,
Byelorussia
Edgar HAAK
Polli Horticultural Research Centre of the Institute of Agricultural and
Environmental Sciences of the Estonian University of Life Sciences,
Karksi-Nuia 69104, Estonia. E-mail: [email protected].
In the frame of Baltic fruit rootstock studies program apple trees of cultivar ‘Auksis’
(Malus domestica Borkh.) grown on 12 dwarf rootstocks were planted in Estonia, Latvia,
Lithuania and Byelorussia in 2001 and evaluated for five years. Dwarf rootstocks included
four selections from the Budagovski series (B.9, B.146, B.396, B.491), three from the Polish
series (P 2, P 22, P 60), M.9, M.26, York 9, Bulboga (Moldavian selection) and Pure 1
(Latvian selection). The strongest tree growth was recorded in Lithuania and Byelorussia.
The highest yields were obtained in Lithuania. All tested rootstocks according growth
vigour control can be grouped in the following way: less vigour than M.9 – P 22, the same
as M.9 – Pure 1, B.396, York 9, P.60, B.9 and P 2, between M.9 and M.26 – B.491, the same
or more vigorous as M.26 – Bulboga and B.146. Trees on rootstocks Pure 1 gave the
highest cumulative yield and were the most efficient although there was no significant
difference in cumulative fertility index with trees growing on rootstocks P 22, P 2, M.9, B.9
and York 9. The least efficient were trees on rootstocks Bulboga and B.146. Rootstock and
location interaction was recorded for B.491 and P.60 in growth vigour control, York 9 in
total yield, and B.9 in yield efficiency.
Key words: Malus domestica Borkh., growth, yield, fertility index, geographical
location.
334
Introduction. The Baltic fruit rootstock studies program was initiated in 1998
and first trials planted in Latvia, Lithuania, Estonia and Byelorussia in 2001 (Bite et
al., 2004). The main attention in this program is paid to evaluation of apple rootstocks.
Rootstock influence on tree performance depends on many factors: soil, climate,
moisture, orchard management and etc. For this reason series of multi-site rootstock
trials were established around the world (Autio et al., 2001; Maas, Wertheim, 2004;
Robinsson et al., 2003, 2004; Wertheim, Callesen, 2000).
In some multi-site trials it was established that site has the predominant influence
on tree performance (Hirst, 2001; Hirst et al., 2001). There were observed that
rootstock and location interacted to affect yield per tree and yield efficiency (Autio
et al., 1990).
It is important to have knowledge of this type of variation in rootstock
performance when making recommendations to apple growers.
The objective of the research was to study the effect of rootstocks on the
growth and productivity of apple trees in different geographical locations and
environmental conditions in North-East part of Europe.
Materials and methods. The trial was carried out in Babtai, Lithuanian Institute
of Horticulture (LT), Pure Horticultural Research Centre (LV), Polli Research Centre
of the Institute of Agricultural and Environmental Sciences of the Estonian University
of Life Sciences (EST), and Pruzany, Brest Agricultural Experimental Station (BY)
in 2001-2005. The geographical locations are following: Babtai in Lithuania
55° 60’ N, 23° 48’ E, Pure in Latvia 57° 02’N, 22° 52’E, Polli in Estonia 58° 67’N,
25° 33’E, and Pruzhany in Belarus, 52° 33’ N, 24° 28’ E. The soil humus content in
Lithuania was 2.5%, P2O5 – 255 mg per kg, K2O 230 mg per kg, in Latvia the soil
humus content was 1.8%, P2O5 – 189 mg per kg, K2O – 151 mg per kg., in Byelorussia
the soil humus content was 3.71%, P2O5 – 397 mg per kg, K2O – 288 mg per kg.
Twelve vegetative propagated apple rootstocks M.26, M.9, York 9, B.9, B.396
(original name 62-396), B.146 (original name 57-146), B.491 (original name
57-491), P 60, P 22, P 2, Bulboga (Moldavian selection) and Pure 1 (Latvian selection)
were tested with cultivar ‘Auksis’. Planting material was produced in the nursery of
Pure Horticultural Research Centre.
The orchards were planted in the spring of 2001 under the same scheme. Planting
distances were 4x1.5 m. Trees were trained as slender spindles. The trial consisted
of four replications with 3 trees in each. Replications were randomised.
Tree growth was evaluated by stem diameter (mm), 30 cm above soil surface.
Tree productivity was calculated as kg cm-2 of TCSA (tree cross sectional area)
every year and cumulative fertility index (kg cm-2 of TCSA) was counted. Variance
analysis was done with a LSD test using the ANOVA statistical program. Because of
the inherent differences in variance among sites and for ease of analysis rootstock
effects were analyzed individually according to location.
In 2002 and 2004 spring frost-damaged blossoms and yield was not evaluated
in Latvia and Estonia. For the same reason very low apple yield was recorded in
Byelorussia in 2003 and in Lithuania in 2004.
Results. G r o w t h. Tree vigour was affected significantly by location.
Trees in Lithuania and Byelorussia had the largest trunk diameter after 5 years, and
335
those in Latvia and Estonia had the smaller trunk diameter (Table 1).
T a b l e 1. Trunk diameter and increase of trunk diameter, mm
1
l e n t e l ë. Kamieno skersmuo ir jo padidëjimas, mm
Trunk diameter in 2005
Increase of trunk diameter, 2001–2005
Kamieno skersmens padidëjimas 2001–2005 m.
Kamieno skersmuo 2005 m.
Rootstock
Poskiepis
LV
LT
EST
BY
average
LV
LT
EST
BY
average
M.9
33.5
40.1
31.5
43.1
37.0
19.3
22.3
18.0
29.6
22.3
M.26
42.6
51.0
39.8
52.7
46.5
24.9
33.0
23.8
36.0
29.4
B.146
47.7
58.2
42.0
53.4
50.3
26.0
39.0
23.0
34.3
30.6
Pure 1
36.9
41.3
32.8
41.4
38.0
17.5
23.1
16.5
25.2
20.6
B.396
35.2
38.0
35.3
42.4
37.7
19.7
21.4
20.5
28.1
22.4
York 9
35.1
43.0
32.5
41.4
38.0
16.2
23.7
14.5
23.6
19.5
P 60
38.7
44.2
30.5
46.3
39.9
23.3
26.2
17.5
30.6
24.4
Bulboga
47.3
63.3
49.3
58.3
54.5
27.2
40.4
32.8
40.6
35.3
B.9
36.4
45.0
31.3
41.9
38.7
19.6
24.7
16.5
26.5
21.8
B.491
35.1
46.0
37.0
51.2
42.3
19.3
28.7
22.5
35.9
26.6
P 22
28.4
35.1
26.0
38.4
32.0
12.2
16.1
13.5
22.4
16.1
P2
35.6
37.2
-
40.1
37.6
20.4
21.4
-
25.6
22.5
Average
37.7
45.1
35.3
45.9
20.5
26.7
19.9
29.9
3.85
4.62
3.87
4.43
2.52
2.15
1.91
2.43
Vidurkis
LSD05/R05
vidurkis
vidurkis
Rootstock P 22 produced the smallest trees in all locations whereas Bulboga
and B.146 produced the largest trees. For rootstock B.491 interaction between location
and rootstock was observed. In Latvia its trunk diameter was similar to M.9, in
Estonia and Byelorussia was similar to M.26. P 60 in Estonia grew as M.9, in other
3 places it was significantly more vigorous.
Bulboga, B.146 and M.26 had the biggest trunk diameter increase during the
five years in the orchard in all locations. The smallest increase was recorded for
P 22. Some interactions between rootstock and location occurred: P 60 determined
significantly bigger increase of trunk diameter than M.9 in Latvia and Lithuania,
while in Estonia and Byelorussia they were similar. Rootstock B.491 grew in Latvia
as M.9 but in other three locations significantly stronger.
Y i e l d. The greatest cumulative (2002-2005) yield per tree was obtained in
Lithuania, and the lowest one was obtained in Latvia and Estonia (Table 2). Trees on
rootstock Pure 1 yielded the most in Latvia and Lithuania. In Estonia rootstock Pure
1 together with Bulboga gave the highest yield too. B.9 gave the highest yield in
Byelorussia and was second in Latvia. York 9 performed well in Lithuania and Estonia,
336
but gave lower yield than trial mean in Latvia. Rootstock P60 showed good yielding
capacity in Latvia and Byelorussia, average – in Lithuania and lower in Estonia.
Rootstock M.9 in three places averaged trial mean or less as in Latvia did. P 22
showed the lowest cumulative yield in Latvia and Estonia, and P 2 – in Lithuania and
Byelorussia.
Overall in all places trees on rootstock Pure 1 gave the biggest yield, followed by
Bulboga and York 9. The lowest cumulative yield was obtained from trees on P 22.
T a b l e 2. Rootstock effect on cumulative yield (kg/tree) of apple cv.
‘Auksis’ in 2002–2005 depending on geographical location
2
l e n t e l ë. Poskiepiø átaka ‘Auksio’ veislës obelø suminiam derliui (kg/vaism.)
esant ávairioms agroklimatinëms sàlygoms
Rootstock / Poskiepis
LV
LT
EST
BY
Average / Vidurkis
M.9
3.77
31.59
7.0
11.72
13.52
M.26
6.76
31.23
9.2
12.36
14.88
B.146
4.39
33.85
6.1
11.10
13.86
Pure 1
9.56
41.33
9.5
11.04
17.85
B.396
3.58
26.13
7.5
11.54
12.18
York 9
4.69
37.25
9.4
11.40
15.68
P 60
8.04
31.59
6.9
13.02
14.88
Bulboga
5.97
35.14
10.4
11.93
15.86
B.9
7.46
31.04
6.7
14.30
14.87
B.491
3.44
27.96
6.6
9.14
11.78
P 22
3.17
25.48
6.2
9.20
11.01
P2
3.47
23.27
-
8.72
11.82
Average / Vidurkis
5.36
31.32
7.8
11.29
14.00
1.21
4.22
1.45
2.34
LSD05/R05
P r o d u c t i v i t y. The most yield efficient trees were in Lithuania and the
least efficient trees were in Latvia (Table 3).
Trees on Pure 1 were the most efficient in Latvia, Lithuania and Estonia. Highly
efficient trees in Lithuania were on rootstocks P 22, York 9, M.9, P 2 and B.9 too. In
Latvia higher efficiency showed B.9 and P 60, in Estonia similar efficiency as Pure 1
was on rootstocks P 22 and York 9. B.9 was significantly more efficient than other
rootstocks in BY.
Overall, trees on Pure 1 were the most efficient, although trees growing on
rootstocks P 22, P 2, M.9, B.9 and York 9 were similar. Trees on Bulboga and B.146
were the least efficient and they were the least efficient rootstocks in all locations.
337
T a b l e 3. Rootstock effect on cumulative fertility index (kg cm-2 of
TCSA) of apple cv. ‘Auksis’ in 2002–2005 depending on
geographical location
3
l e n t e l ë.
Poskiepio átaka ‘Auksio’ veislës suminiam produktyvumo indeksui
(kg cm -2 kamieno skerspjûvio ploto) esant ávairioms
agroklimatinëms sàlygoms
Rootstock / Poskiepis
LV
LT
EST
BY
Average /Vidurkis
M.9
0.52
3.29
0.92
1.28
1.50
M.26
0.52
1.97
0.73
0.88
1.03
B.146
0.27
1.50
0.36
0.79
0.73
Pure 1
1.01
3.86
1.13
1.22
1.81
B.396
0.40
2.92
0.77
1.27
1.34
York 9
0.53
3.22
1.15
1.14
1.51
P 60
0.75
2.68
0.93
1.18
1.39
Bulboga
0.37
1.36
0.55
0.68
0.74
B.9
0.82
3.01
0.89
1.58
1.58
B.491
0.43
2.21
0.62
0.75
1.00
P 22
0.57
3.68
1.17
1.13
1.64
P2
0.43
3.11
-
1.04
1.53
Average / Vidurkis
0.55
2.73
0.84
1.08
1.32
0.15
0.50
0.18
0.24
LSD05/R05
Discussions. Obtained results clearly illustrate that the vigour and tree
productivity induced by rootstocks depend on local climatic and soil conditions.
Proper evaluation of rootstocks requires establishment of rootstock testing trials at
different locations.
All tested rootstocks according growth vigour control can be grouped in the
following way: less vigour than M.9 – P 22, the same as M.9 – Pure 1, B.396, York
9, P 60, B.9 and P 2, between M.9 and M.26 – B.491, the same or more vigorous as
M.26 – Bulboga and B.146. Such rootstock vigour range in some cases contradicts
to results obtained in other trials, especially with rootstocks Budagovski. In
Netherlands B.146 and B.491 are recorded as less vigorous than M.9 (Maas, Wertheim,
2004). In Great Britain B.146 produced trees that were more dwarfed than on
M.27-EMLA. (Webster, Holland, 1999) and in USA B.491 was equal to P 22 and
M.27 EMLA (Hirst, 2001).
Rootstock interacted significantly with location affecting tree growth. More
vigorous apple tree growth was recorded following North-South direction; however,
the relative differences among rootstock within locations were similar and only some
interactions occurred.
338
Cumulative yield varied between trial places. The highest yields were obtained
in Lithuania – three times bigger than in Byelorussia and 5-6 times than in Latvia and
Estonia. The reason of such differences was severe spring frosts that damaged
flowers and fruitlets in 2002 and 2004.
Rootstock Pure 1 gave the greatest cumulative yield and had the highest fertility
index. Pure 1 showed as the best rootstock in three places, except Byelorussia. Such
findings overcome the results in earlier performed trials where rootstocks Pure 1
and B 9 had similar influence on tree vegetative growth and yields (Lepsis, 2004). In
spite of productivity other characteristics of rootstock Pure 1, especially fruit quality,
must be tested more carefully.
The smallest trees tended to have the lowest yields per tree with the exception
of Pure 1 and York 9, therefore typically trees growing on rootstocks P 22, and P 2
had the lowest yields at each site. On the other hand, the smallest trees usually are
the most productive, what is declared in many trials (Kviklys, 2002; Kviklys et al.,
1999). The same tendency was recorded in our trials too. The least productive trees
were on strong growing rootstocks – Bulboga, B.146, B.491 and M.26.
In many multi-site trials interactions between rootstocks and location are recorded
(Maas, Wertheim, 2004; NC-140, 1996a; NC-140, 1996b). Although the results
reported for the overall study conducted over 12 locations throughout the U.S. suggest
that the relative importance of the interaction of cultivar and location is low, however,
this study did not include locations with dramatically different climatic conditions
(Autio et al., 2001b). Greater interactions between rootstock and location may be
seen if more divergent locations are included (Autio et al., 1990). In our trials
interactions between rootstock and location was recorded for B.491 and P 60 in
growth vigour control, York 9 in total yield, and B.9 in yield efficiency.
Conclusions. 1. Rootstocks Bulboga, B.146, and M.26 depend to semi-dwarf
rootstock group.
2. Rootstocks Pure 1, B.396, York 9, P.60, B.9 and P 2 are in the same vigour
group as M.9.
3. Trees on rootstocks Pure 1 gave the highest cumulative yield and were the
most efficient. The least efficient were trees on Bulboga and B.146 rootstocks.
4 Rootstock and location interaction was recorded for B.491 and P 60 in growth
vigour control, York 9 in total yield, and B.9 in yield efficiency.
Acknowledgement. This work was partly supported by Lithuanian State Science
and Studies Foundation.
Gauta
2006 06 08
Parengta spausdinti
2006 07 13
339
References
1. A u t i o W. R., L o r d W. J., V e n e m a n P. L. M. Rootstock and
site influence performance of ‘McIntosh’ apple trees. HortScience. 1990. 25. P. 1219-1221.
2. A u t i o W. R., A n d e r s o n J. L., B a r d e n J. A., B r o w n G.
R., C r a s s w e l l e r R. M., D o m o t o P. A., E r b A., F e r r e e D. C.,
G a u s A., H i r s t P. M., M u l l i n s C. A., S c h u p p J. R. Performance
of ‘Golden Delicious’, ‘Jonagold’, ‘Empire’, and ‘Rome Beauty’ apple trees on five
rootstocks over ten years in the 1990 NC-140 cultivar/rootstock trial // Journal of the
American Pomological Society. 2001 a. 55(3). P. 131-137.
3. A u t i o W. R., A n d e r s o n J. L., B a r d e n J. A., B r o w n G.
R., C r a s s w e l l e r R. M., D o m o t o P. A., E r b A., F e r r e e D. C.,
G a u s A., H i r s t P. M., M u l l i n s C. A., S c h u p p J. R. Location
affects performance of ‘Golden Delicious’, ‘Jonagol’, ‘Empire’, and ‘Rome Beauty’ apple
trees on five rootstocks over ten years in the 1990 NC-140 cultivar/rootstock trial // Journal
of the American Pomological Society. 2001 b. 55(3). P. 138-145.
4. B i t e A., K v i k l y s D., U n i v e r T., L u k u t T. The beginning of
the project “Baltic fruit rootstock studies” // Acta Horticulturae. 2004. 658(1). P. 437-440.
5. M a a s F. M., W e r t h e i m S. J. A multi-site rootstock trial with the
apple cultivars ‘Cox’s Orange Pippin’ and ‘Jonagold’ // Acta Horticulturae. 2004. 658(1).
P. 177-184.
6. H i r s t P. M. Early Performance of ‘Gala’ on 18 dwarf and 4 semi-dwarf
rootstocks growing at 24 sites in North America. Acta Hort. (ISHS). 2001. 557. P. 199-208.
7. H i r s t P. M., A u t i o W. R., B a r d e n J. A., B r o w n G. R.,
C r a s s w e l l e r R. M., D o m o t o P. A., S c h u p p J. R. Performance of
trees in the 1990 NC-140 apple cultivar/rootstock planting: additional cultivars and
rootstocks. Journal of the American Pomological Society. 2001. 55. P. 178-184.
8. K v i k l y s D. Apple rootstock research in Lithuania with aspect to fruit quality
and tree productivity // Sodininkystë ir darþininkystë. 2002. 21(3). P. 3-13.
9. K v i k l y s D., U s e l i s N., K v i k l i e n ë N. Rootstock effect on
‘Jonagold’ apple tree growth, yield and fruit quality // Apple rootstocks for intensive
orchards. Warszawa, 1999. P. 67-69.
10. L e p s i s J. Evaluation of the apple clonal rootstock Pure 1 in the orchard with
different pruning and training systems // Acta Horticulturae. 2004. 658. P. 173-176.
11. N C - 1 4 0. Performance of the NC-140 Cooperative Apple Rootstock Planting:
I. Survival, tree size, yield and fruit size // Fruit Variety journal. 1996a. 50. P. 6-11.
12. N C - 1 4 0. Performance of the NC-140 Cooperative Apple Rootstock Planting
II: A 10- year summary of TCA, yield and yield efficiency at 31 sites // Fruit Variety journal.
1996 b. 50. P. 11-18.
13. R o b i n s o n T. L., A n d e r s o n L., A z a r e n k o A., B a r r i t t
B. H., B r o w n G., C l i n e J., C r a s s w e l l e r R., D o m o t o P.,
E m b r e e C., F e n n e l l A., F e r r e e D., G a r c i a E., G a u s A.,
G r e e n e G., H a m p s o n C., H i r s t P., H o o v e r E., J o h n s o n S.,
K u s h a d M., M a r i n i R. E. Performance of Cornell-Geneva rootstocks across
North America in multi-location NC-140 rootstock trials // Acta Horticulturae. 2004. 658.
P. 241-245.
340
14. R o b i n s o n T., A n d e r s o n L., A z a r e n k o A., B a r r i t t B.,
B a u g h e r T., B r o w n G., C o u v i l l o n G., C o w g i l l W.,
C r a s s w e l l e r R., D o m o t o P., E m b r e e C., F e n n e l l A., G a r c i a
E., G a u s A., G r a n g e r R., G r e e n e G., H i r s t P., H o o v e r E.,
J o h n s o n S., K u s h a d M. Performance of Cornell-Geneva apple rootstocks
with Liberty as the scion in NC-140 trials across North America // Acta Horticulturae. 2003.
622. P. 521-530.
15. W e b s t e r A. D., H o l l a n d s M. S. Apple rootstock studies:
comparison of Polish, Russian, USA and UK selections as rootstocks for the apple cultivar
Cox’s Orange Pippin (Malus domestica Borkh.) // The Journal of Horticultural Science
and Biotechnology. 1999. 74(3). P. 367-374.
16. W e r t h e i m S. J., C a l l e s e n O. Results of multi-site interstem trials
with apple trees. Gartenbauwissenschaft. 2000. 65(6). P. 251-259.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
334–341.
BALTIJOS POSKIEPIØ TYRIMAI: 12 POSKIEPIØ ÁVERTINIMAS
ATLIEKANT TYRIMUS SU ‘AUKSIO’ VEISLËS OBELIMIS
D. Kviklys, N. Kviklienë, A. Bite, J. Lepsis, T. Lukut, E. Haak
Santrauka
Vykdant Baltijos poskiepiø tyrimø programà, 2001 m. ‘Auksio’ veislës obelø su 12
þemaûgiø poskiepiø sodai buvo áveisti Latvijoje, Lietuvoje, Estijoje ir Baltarusijoje. Tirti
Rusijos Budagovskio selekcijos poskiepiai B.9, B.146, B.396 ir B.491, Lenkijos P serijos
poskiepiai P 2, P 22 ir P 60, Vokietijos York 9, Latvijos Pure 1, Moldovos Bulboga bei M.9
ir M.26 poskiepiai. Veðliausiai vaismedþiai augo Lietuvos ir Baltarusijos sàlygomis, o
gausiausiai derëjo Lietuvoje. Pagal vaismedþiø augumo ribojimà poskiepiai sugrupuoti ðia
tvarka: maþesni uþ M.9 – P 22, tokio pat augumo kaip M.9 – Pure 1, B.396, York 9, P 60, B.9
ir P 2, tarpiniai tarp M.9 ir M.26 – B.491, tokio pat augumo kaip M.26 – Bulboga ir B.146.
Didþiausià suminá derliø davë vaismedþiai su Pure 1 poskiepiu. Jie buvo ir produktyviausi,
nors vaismedþiø su P 22, P 2, M.9, B.9 ir York 9 poskiepiais suminio produktyvumo esminiø
skirtumø nenustatyta. Maþiausiai produktyvûs buvo Bulboga ir B.146 poskiepiai.
Nustatytos sàveikos tarp poskiepio ir auginimo vietos: vaismedþiø augumo ribojimo –
poskiepiai B.491 ir P 60, suminio derliaus – York 9, produktyvumo – B.9 poskiepis.
Reikðminiai þodþiai: augumas, derlius, geografinë vietovë, Malus domestica Borkh.,
produktyvumo indeksas.
341
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 342–349.
EVALUATION OF APPLE ROOTSTOCK-CULTIVAR
COMBINATIONS BY GROWTH RHYTHMS COINCIDENCE
Mintauts ABOLINS
Department of Horticulture, Latvia University of Agriculture, 2 Liela,
Jelgava, LV–3001, Latvia. E-mail: [email protected]
Five cultivars ‘Baltais Dzidrais’, ‘Konfetnoje’, ‘Tiina’, ‘Lobo’ and ‘Sinap Orlovskij’
were used grafted on rootstocks B.9, B.490 and B.118 for 20 to 30 combinations in each
treatment. Records of monthly growth rhythms were made within seven days to ten plants
in each treatment, measuring both the graft and rootstocks shoot. Auxanographs were
carried out for two 24-hours periods in the most characteristic phenophases of the
vegetative shoots: increased growth, maximum growth, retarded growth and in the phase
between maximum and retarded growth. The best coincidence between rootstock
and cultivars of the monthly growth rhythms was observed for combinations ‘Sinap
Orlovskij’/B.9 and ‘Tiina’/B.9 – four waves coincided. Medium coincidence was observed
for combinations ‘Sinap Orlovskij’/B.490, ‘Tiina’/B.490 and ‘Baltais Dzidrais’/B.118, and
worst – only one wave coincided - for combinations ‘Baltais Dzidrais’/B.9 and ‘Lobo’/B.9.
The best coincidence of diurnal growth rhythms was observed for combinations
‘Tiina’/B.490 and ‘Baltais Dzidrais’/B.118, respectively 75.0 and 62.5%. Medium good
coincidence of 50% was obtained for combinations ‘Sinap Orlovskij’/B.490, ‘Lobo’/B.9
and ‘Baltais Dzidrais’/B.9. A low correlation (r=0.12) was obtained for the combination
‘Baltais Dzidrais’/B.9, which showed the worst coincidence in the diurnal growth rhythms.
A low coincidence of growth rhythms was found for cultivars ‘Sinap Orlovskij’ and ‘Tiina’
grafted on B9, but the high correlation (r=0.72 to 0.76) showed medium good coincidence.
Key words: apple-tree, growth rhythms, coincidence, compatibility.
Introduction. In nature, plant growth is a rhythmical process, which is regulated
by plants inner clockwork computed into plant genes. Plant growth is connected
with physiological and biochemical fluctuation (Cumming, Wagner, 1968).
The plant growth rhythm is characterized by the frequency of periods and
amplitude. Depending on amplitude, growth rhythms are subdivided into six units:
the growth period lasting for several years; a year’s rhythm; a month’s or week’s
rhythm; lunar rhythm; diurnal rhythm and small units rhythm or pulsation (Bünning,
1977). Attempts to change the rhythmical process by some experiments were
unsuccessful.
The plant growth is normal if the changes of environmental factors are
synchronous with plant growth rhythms. It is significant for grafted plants because
342
grafted plants combine two genotypes in one-unit – graft and rootstock and therefore
they are more sensitive to environmental factors. Comparing seedling or clonal
rootstocks, more sensitive are the clonal rootstocks (Abolins, 2001). There are
different clonal rootstock genotypes that indicate specific rootstock – graft interaction.
Interaction is expressed as compatibility or incompatibility between graft components.
Clonal genotypes of rootstocks are more plastic, with wide modificative variability,
but some with narrow. There is no universal rootstock, which can match all or the
majority of cultivars (Webster, 1993). There are two forms of incompatibility: distinct
form and hidden form of incompatibility. The distinct forms of incompatibility are:
breaking of trees at the point of union after they have been growing for some years
(apricot on Pr. cerasifera); appearance of disease symptoms (necroses and others);
premature death of the trees.
The hidden forms of incompatibility are expressed by: retarded growth of the
new plants in the nursery; premature yellowing of the leaves in autumn, followed by
early defoliation (‘Baltais Dzidrais’/B.9); the scion overgrows the stock; the stock
overgrows the scion; suckering of rootstock (expressed for plums); marked differences
in growth rate or vigour of scion and rootstock.
There are no universal methods for testing hidden incompatibility. Some of the
methods are electrophoresis test (Santamour, McArdle, Jaynes, 1986) and magnetic
resonance imaging (Warmund et al., 1993). The use of a couple methods is more
reliable. Some researchers show that the growth rhythm of fruit trees may change in
case of hidden incompatibility (Moreno et al., 1993; Errea et al., 1994). In this article
growth rhythms of rootstocks and grafts are presented.
Materials and methods. Investigation was carried out at the Horticulture
Training and Research Unit of the Department of Horticulture in 2004–2005.
Five cultivars ‘Baltais Dzidrais’, ‘Konfetnoje’, ‘Tiina’, ‘Lobo’ and ‘Sinap
Orlovskij’ grafted on rootstocks B.9, B.490 and B.118 for 20 to 30 combinations in
each treatment were investigated.
Records for monthly growth rhythms were made within seven days, measuring
both the graft and the rootstock’s shoot.
For the precise determination of the growth rhythms of both rootstock and
graft, the simultaneous measurement should be done to each plant for both graft and
rootstock shoot. To achieve this, the following was done: in spring, at the beginning
of vegetation period, grafted buds and rootstock shoots were permitted to grow. For
each treatment, plants similar in buds and rootstock shoots were selected. Records
of monthly or weekly growth rhythms were made within seven days for ten plants in
each treatment.
The diurnal growth rhythms were observed by the auxanography method
developed by the author (Abolins, 2001). Auxanography was carried out for two
24 hour period during the most characteristic phenophases of the vegetative shoots:
increased growth, maximum growth, retarded growth and in the phase between
maximum and retarded growth. A total of 24 auxanographs were used and 400
auxanograms were obtained.
Obtained results were used to calculate the mean elongation of both shoot types
every two hours. Coincidence of diurnal rhythms was evaluated by density of the
343
sinusoidal growth curve, the coincidence of growth maximum and minimum for the
shoots of graft and rootstock. The coincidence of growth maximums and minimums
was expressed in percentage.
The height and diameter of grafted plants were measured at the end of the
vegetation period. Evaluation of roots was noted by a nine point scale: 0 – undeveloped
roots; 9 – the roots are excellent. For mathematical data processing ANOVA software
used, correlations, variation and LSD values were calculated.
Results and discussion. The growth rhythms of graft and rootstock shoot
height varied from 2 to 4 month waves. The number of growing waves was influenced
by genotypes of cultivars and rootstock. Four growing waves for cultivars ‘Sinap
Orlovskij’ on B.9 were well expressed. The amplitude of month’s rhythm varied
from 14 to 21 days. Good coincidence between graft and rootstock was noted
(r=0.755). A total growth of 106.6 cm was noted for graft compared to rootstock
shoot growth of 70 cm (Fig.1). The course of the month’s rhythm was similar for
the same cultivars ‘Sinap Orlovskij’ grafted on B.490 except for the first growth
wave, which did not correlate (r=0.497). Four growing waves were noted for grafting
combinations ‘Tiina’/B.9, but only two waves were better expressed. The total growth
for cultivars ‘Tiina’ and rootstock B.9 were similar. The cultivar’s growth was more
intensive for combination ‘Tiina’/B.490. The correlation between graft and rootstock
B9 was high (r=0.953).
F i g. 1. Good coincidence of month rhythms between cultivar ‘Sinap Orlovskij’ and
rootstock B.9
1
p a v. Geras ‘Sinap Orlovskij’ veislës ir B.9 poskiepio mënesio augimo ritmø
sutapimas
Three growing waves were noted for ‘Baltais Dzidrais’, but only two for rootstock
B.9. The growth of cultivars was more intensive compared to rootstock shoot.
There was noted a low coincidence between grafting combinations (Fig. 2). Results
of coincidence for ‘Baltais Dzidrais’ were better with rootstock B.118. The worst
coincidence of month rhythm was observed for cultivars ‘Lobo’ grafted on B.9. It
344
was mainly associated with differences of growth waves number and the thin growth
of rootstock shoot (r=0.399).
F i g. 2. Worst coincidence of month rhythms between cultivar ‘Baltais Dzidrais’
and rootstock B.9
2
p a v. Blogiausias ‘Baltais Dzidrais’ veislës ir B.9 poskiepio mënesio augimo ritmø
sutapimas
The results obtained in auxanography showed rhythmic diurnal growth of apple
cultivars and clonal rootstocks with the curve resembling sinusoid. Maximum growth
for cultivars ‘Tiina’ and rootstock shoot B.9 were recorded in the evening hours,
from 6 to 8 p.m., but the minimum growth was observed in the morning from 8 to
10 a.m. (Fig. 3).
F i g. 3. Diurnal growth rhythm of apple tree in the phase of maximum growth
3
p a v.
Obels dienos augimo ritmas maksimalaus augimo tarpsniu
345
The best coincidence of diurnal growth rhythm considering growth maximum
and minimum was noted for cultivars ‘Tiina’ grafted on B.490 and ‘Baltais
Dzidrais’/B.118, respectively 75.0 and 62.5% (Fig. 4, Table 1). The medium good
coincidence – 50% was noted for cultivars ‘Sinap Orlovskij’/B.490, ‘Lobo’/B9 and
‘Baltais Dzidrais’/B.9. However, low correlation (r=0.120) is obtained for combination
‘Baltais Dzidrais’/B.9, which showed worst coincidence in diurnal growth rhythm.
Coincidence of growth rhythm – only 37% – was noted for combinations ‘Sinap
Orlovskij’/B.9 and ‘Tiina’/B.9, but the correlation is high, r=0.72-0.76. Good
coincidence for all combinations was observed in the phase of maximum growth,
but lowest in the phases of increased and retarded growth (Table 1). This is in
agreements with our and others investigations showing that hidden incompatibility
between graft and rootstock find expression when environmental conditions are not
suitable, mainly with low temperature.
F i g. 4. Diurnal growth rhythm of apple tree in the phase of maximum growth
4
p a v.
Obels dienos augimo ritmas maksimalaus augimo tarpsniu
Analysed results of grafting showed that the best results were obtained for
cultivars ‘Lobo’ 73.1 and ‘Tiina’ 68.0%, but worst for ‘Baltais Dzidrais’ on B.9 –
54.5% (Table 2). Better results were obtained for cultivars grafted on semi-dwarfing
rootstocks, comparing with dwarfing rootstock B.9. For all combinations they were
71.40 to 81.50%, except cultivars ‘Konfetnoje’ on B.490 – 64.20%. Results of grafting
are not always the main parameter for testing compatibility. Some other combinations
could be influenced, but in our experiments combination ‘Baltais Dzidrais’ on B.9
showed correlation between coincidence of growth rhythm and results of grafting.
Qualitative features of one-year-old apple planting material – tree height and
stem diameter for all cultivars on B.9 were optimal, except cultivars ‘Tiina’ on B.9.
The height of ‘Tiina’ was only 65.80 cm. The greatest height for cultivars grafted on
semi-dwarfing rootstocks was obtained for ‘Konfetnoje’, ‘Tiina’ and ‘Sinap Orlovskij’:
115.5 to155.7 cm. The greatest height of stem obtained for combinations ‘Lobo’
and ‘Sinap Orlovskij’ grafted on B.9, but lowest for ‘Baltais Dzidrais’ on the same
rootstock. Significant differences for cultivars grafted on semi-dwarfing rootstock
were not obtained.
The height of cultivars in nursery not always showed hidden incompatibility
346
between graft and rootstock. Sometimes it is retarded, but sometimes it could be
high. This is in agreement with other investigations (Hartmann et al., 1997).
T a b l e 1. Coincidence of diurnal growth rhythms of rootstockcultivar combinations
1
l e n t e l ë. Poskiepio ir veislës deriniø dienos augimo ritmø sutapimas
Coincidence
Sutapimai, %
r (p=0.05)
Sulëtëjæs
augimas
Retarded growth
r (p=0.05)
Tarp. fazë
Inter-phase
r (p=0.05)
Maksimalus
augimas
Maximum
growth
r (p=0.05)
Spartus augimas
Increased
growth
Augimo maksimumai ir minimumai; augimo tarpsniai
Deriniai
Combinations
Growth rate maximum and minimum; phases of growth
‘Sinap
Orlovskij’/B.9
-/-
0.75
-/+
0.85
+/-
0.84
+/-
0.72
37.5
‘Sinap
Orlovskij’/B.490
-/+
0.92
+/+
0.97
+/-
0.88
-/-
0.62
50.0
‘Tiina’/B.9
+/+
0.77
-/+
-
-/-
0.34
-/-
0.76
37.5
‘Tiina’/B.490
+/+
0.86
+/+
0.90
+/+
0.95
-/-
0.17
75.0
‘Baltais
Dzidrais’/B.9
+/-
0.55
+/+
0.68
+/-
0.86
-/-
0.12
50.0
‘Baltais
Dzidrais’/B.118
+/-
0.90
+/+
0.94
+/-
0.91
-/+
0.07
62.5
‘Lobo’/B.9
-/-
0.90
-/-
0.89
+/+
0.96
+/+
-
50.0
Signs: + coincidence of growth rhythms; – not coincidence
Simboliai: + augimo ritmø sutapimas; – nesutapimas
The testing of roots showed that more intensive growth was obtained for
cultivars ‘Lobo’, ‘Sinap Orlovskij’ and ‘Tiina’, comparing with ‘Baltais Dzidrais’
and ‘Konfetnoje’ grafted on B.9. For all cultivars grafted on semi-dwarfing rootstock
the growth of roots were more intensive.
347
T a b l e 2. Grafting results growth of one-year-old planting material
2
l e n t e l ë. Skiepijimo rezultatai ir vienameèiø sodinukø augimas
Results of
grafting
Combinations
Deriniai
Skiepijimo
rezultatai, %
Tree height
Vaismedžio
aukštis, cm
Stem diameter
Kamieno
skersmuo, mm
Roots, points 0-9
Šaknys balais (0–9)
Dwarfing rootstocks / Þemaûgiai poskiepiai
‘Baltais Dzidrais’/B.9
54.5
104.1
15.70
5.20
‘Konfetnoje’/B.9
64.9
94.8
16.20
5.40
‘Lobo’/B.9
73.1
96.4
21.56
7.60
‘Sinap Orlovskij’/B.9
61.8
106.6
18.40
7.40
‘Tiina’/B.9
68.0
65.8
17.20
6.70
Semi-dwarfing rootstocks / Pusiau þemaûgiai poskiepiai
‘Baltais Dzidrais’/B.118
71.4
120,5
18.75
7.90
‘Konfetnoje’/B.490
64.2
122,7
17.31
8.70
‘Lobo’/B.’490
81.5
115,5
17.99
8.50
‘Sinap Orlovskij’/B.490
80.6
155.7
18.70
9.00
‘Tiina’/B.490
80.8
115.5
17.09
8.30
-
22.7
2.56
0.83
LSD 05/R05
Conclusions. 1. The course and coincidence of growths rhythms of cultivars
and rootstocks varied between growth phenophases. The lowest coincidence was
obtained in the phases of increased and retarded growth.
2. The coincidence of cultivars and rootstocks month and diurnal growth rhythm
may be one of indices of hidden incompatibility.
Gauta
2006 05 15
Parengta spausdinti
2006 07 27
References
1. A b o l i n s M. Investigations of apple cultivars – rootstock growth rhythms
for determination of graft component compatibility. 6th Intl. Symp. Fruit, Nut and Veget.
Prod. Eng. Potsdam, Germany. 2001. 11–14 Sept. 101–106.
2. B ü n n i n g E. Die physiologische Uhr (Cirkadiane Rhythmik und
Biochronometrie). Springer - Verlag, Heidelberg, 1977. P. 61–95.
3. C u m m i n g B., W a g n e r E. Rhythmic processes in plants // Annu Rev
Plant Physiol. 1968. 19: 381– 416.
348
4. E r r e a P., F e l i p e A., H e r r e r o M. Graft establishment between
compatible and incompatible Prunus spp. // J. Exper. Bot. 1994. 45 (272): 393–401.
5. H a r t m a n n H. T., K e s t e r D. E. , D a v i e s F. T. et al. Plant
Propagation: Principles and Practice, Prentice Hall, New Jersey, 1997. 700.
6. M o r e n o M., M o i n g A., L a n s a c M. et al. Peach/ myrobalan plum
graft incompatibility in the nursery // J. Hort. Sci. 1993. 68 (5): 705–714.
7. S a n t a m o u r F. S., M c A r d l e A. J. and J a y n e s R. A. Cambial
isoperoxidacepatterns in castanea // J. Environ. Hort. 1986. 4 (1): 14–16.
8. W a r m u n d M. R., B a r r i t t B. H., B r o w n J. M. et al. Detection of
vascular discontinuity in bud unions of ‘Jonagold’ apple on mark rootstock with magnetic
resonance imaging // J. Amer Soc. Hort. Sci. 1993. 118:92–96.
9. W e b s t e r A. D. New dwarfing rootstocks for apple, pear, plum and sweet
cherry // Acta Hort. 1993. 349:145–153.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
342–349.
OBELØ VEISLIØ IR POSKIEPIØ DERINIØ AUGIMO RITMØ SUTAPIMO
ÁVERTINIMAS
M. Abolins
Santrauka
Tirtos penkios veislës (‘Baltais Dzidrais‘, ‘Konfetnoje‘, ‘Tiina‘, ‘Lobo‘ ir ‘Sinap
Orlovskij‘) su B.9, B.490 ir B.118 poskiepiais. Bandyta 20–30 kiekvieno varianto deriniø.
Septynias dienas per mënesá buvo apraðomi deðimties augalø augimo ritmai, iðmatuojant
ir skiepo, ir poskiepio ûglá. Vegetatyviniams ûgliams esant charakteringiausiø fenofaziø –
spartaus augimo, maksimalaus augimo, sulëtëjusio augimo bei fazës tarp maksimalaus ir
sulëtëjusio augimo, du 24 valandø trukmës laikotarpius buvo uþraðomos auksanogramos.
Geriausiai sutapo ‘Sinap Orlovskij’/B.9 ir ‘Tiina’/B.9 poskiepio ir áskiepio deriniø mënesio
augimo ritmai – sutapo keturios bangos. Vidutiniðkai sutapo ‘Sinap Orlovskij’/B.490,
‘Tiina’/B.490 ir ‘Baltais Dzidrais’/B.118 deriniø, blogiausiai, kai sutapo tik viena banga, –
‘Baltais Dzidrais’/B.9 ir ‘Lobo’/B.9 deriniø augimo ritmai. Geriausiai sutapo ‘Tiina’/B.490 ir
‘Baltais Dzidrais’/B.118 deriniø dienos augimo ritmai (atitinkamai 75,0 ir 62,5%), vidutiniðkai
(50%) – ‘Sinap Orlovskij’/B.490, ‘Lobo’/B.9 ir ‘Baltais Dzidrais’/B.9. Gauta maþa ‘Baltais
Dzidrais’/B.9 derinio, kurio dienos augimo ritmai maþiausiai sutapo, koreliacija. Blogai
sutapo ir ‘Sinap Orlovskij’ bei ‘Tiina’ veisliø ir B.9 poskiepio augimo ritmai, taèiau didelë
koreliacija (r=0,72 iki 0,76) parodë, kad sutapimas vidutinis.
Reikðminiai þodþiai: obelys, augimo ritmai, sutapimas, suderinamumas.
349
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 350–356.
MORPHOLOGICAL AND PHYSIOLOGICAL
CHARACTERISTICS OF COLUMNAR APPLE TREES
Bronislovas GELVONAUSKIS, Auðra BRAZAITYTË,
Audrius SASNAUSKAS, Pavelas DUCHOVSKIS,
Dalia GELVONAUSKIENË
Lithuanian Institute of Horticulture, Kauno str. 30, LT–54333 Babtai,
Kaunas distr., Lithuania. E-mail: a.brazaitytë@lsdi.lt
There were investigated two columnar apple cultivars ‘Arbat’ and No. 24217 and
apple cultivar ‘Aldas’ in an orchard at the Lithuanian Institute of Horticulture. The two
latter cultivars were released at the Lithuanian Institute of Horticulture, ‘Arbat’ – in Russia.
Cultivars and selections were budded on rootstocks P 60, M.26 and MM.106. In orchard
apple trees were spaced at 1.0 x 3.5 m. Tree height, stem diameter, total length of one-yearold shoot, leaf area on a tree was measured and number of shoots was calculated.
Chlorophyll and carotenoids content and photosynthesis intensity was detected.
Significant differences for impact of rootstock to tree height, trunk diameter and
shoot number and one-year-old shoot total length were determined. The smallest columnar
apple trees were on rootstocks P 60 but trees ‘Aldas’ were the smallest ones on rootstock
M.26. ‘Aldas’ had the highest number of one-year-old shoots and total length of shoots.
Higher parameters of these traits of all investigated cultivars were estimated on rootstock
MM.106. The highest leaf area of tree was measured for ‘Aldas’ on rootstock MM.106 and
No. 24217 distinguished itself on rootstocks P 60 and M.26. The lowest content of
chlorophyll a+b was estimated for ’Aldas’ on investigated rootstocks. Significant
differences were not detected among cultivars and rootstocks in case carotenoids content.
The highest photosynthesis activity showed No. 24217 on rootstocks MM.106 and P 60
and ‘Arbat’ on M.26.
Key words: carotenoids, chlorophyll, photosynthesis, rootstocks, tree growth.
Introduction. The first columnar apple cultivars were received at East Malling
and were introduced for the private gardening (Tobutt, 1985, 1986). Donors of
columnar growth habit were involved in crosses at the Lithuanian Institute of
Horticulture in 1988 and the first promising hybrids were selected in 1998 and 1999.
Columnar growth apple cultivars usually have few lateral branches and need minimal
pruning in the orchard. Columnar apple cultivars can be useful for gardening, as
pollinizers in commercial orchards or for very high-density plantings (Quinlan, Tobutt;
1990). Apple tree size of cultivars with natural growth habit is controlled by dwarf
350
rootstocks and pruning. Many studies of rootstock influence on fruit tree growth,
productivity and fruit quality have been carried out in different countries around the
world (Kviklys, 2002; Meland et al., 2004; Sadowski et al., 2004; Takacs, 2004,
Robinson and Hoying, 2004). Not so much studies of columnar apple cultivars and
influence of rootstocks on its growth and other characteristics have been done.
Inomata and coworkers (2005) established that columnar apple cultivar ‘Maypole’
tree growth, total shoot length and leaf area was largest on rootstock Marubakaido
followed by M.26 and M27. They concluded that results obtained during the
investigation of columnar type trees grafted on dwarf rootstocks are similar to that
of normal type trees. It was shown that tree height, number of shoots, total shoot
length of columnar type apple trees of evaluated selections were very different (Inomata
et al., 2004). Although the studied selections of columnar type apple trees were more
compact than ‘Fuji’, which has normal type habit. Apple cultivars with columnar
type growth habit are valuable for modern fruit tree production systems because of
reduction of labor in orchard.
The objective of this study was to estimate the influence of dwarf rootstocks to
tree characters and physiological characters of apple cultivars with columnar and
normal type growth habit.
Materials and methods. There were investigated two columnar type habit
apple cultivars and one normal type habit cultivar in an orchard at the Lithuanian
Institute of Horticulture. Columnar apple cultivar ‘Arbat’ and selection No 24217
were released in Russia and normal type habit cultivar ‘Aldas’ – at the Lithuanian
Institute of Horticulture. Cultivars were budded on dwarf rootstocks P 60, M.26 and
MM.106. Trees were planted in an orchard in 2002. Three trees of each cultivar
were used for evaluation. Apple trees were spaced at 1.0 x 3.5 m. Tree height, trunk
diameter, total length of one-year-old shoots, leaf area on a tree was measured and
number of shoots was calculated. Chlorophyll, carotenoids content and photosynthesis
intensity was detected. Leaf area of apple-trees was measured by Portable Leaf Area
Meter CI-202 (CID, Inc., USA). Leaves were pulled of from a shoot segment of
50 cm and leaf area was measured, then tree total shoot length was measured and
tree leaf area was calculated.
Photosynthesis intensity was recorded by Portable Photosynthesis System
CI-310 (CID, Inc., USA). Photosynthesis was measured twice with interval of two
weeks at sixth leaf from shoot top in July. Illumination (FAR) was in both cases
about 2500 mmol m-2 s-1 and temperature – 27.5°C in years of study.
The concentrations of chlorophyll (a + b) were measured in 100% acetone
extract prepared according to Wettstein method (Wettstein, 1957). Three
measurements per sample were done using spectrophotometer Genesys 6
(ThermoSpectronic, USA). Chlorophyll was extracted from 5-6-th fully expanded
leaf from a shoot tip.
Results. In 2003 fruit trees of No. 24217 were the highest on the rootstock
MM 106, fruit trees of ‘Arbat’ – on M.26 and ‘Aldas’ – on P 60 (Table). In 2004 fruit
trees ‘Aldas’ were the highest on all rootstocks. The lowest tree height was recorded
for investigated cultivars, except ‘Aldas’, on rootstock P 60 in 2004. ‘Arbat’ had the
highest trunk diameter on all rootstocks and in both years of study.
351
T a b l e. The traits of apple tree grown on different rootstocks
L e n t e l ë. Su skirtingais poskiepiais augintø obelø poþymiai
Cultivar / Veislë
Tree height
Trunk diameter
Medžio aukštis, cm
Kamieno skersmuo, cm
Shoot number
Ûgliø skaièius
Total shoot length
Ûgliø ilgis, cm
2003
2004
2003
2004
2003
2004
2003
2004
‘Aldas’/MM.106
211.7
5.46
283.7
4.91
-
4.3
0.11
15.3
0.88
33.0
1.00
391.0*
38.18
2086.7
50.89
‘Arbat’/MM.106
199.3
9.67
245.7
10.33
3.3
0.11
4.5
0.00
10.3
0.67
14.0
1.53
298.7
40.54
482.3
16.56
24217/MM.106
215.7
17.65
231.3
10.17
3.1
0.11
4.3
0.24
13.3
2.03
30.7
1.33
320.3
86.23
557.3
21.28
‘Aldas’/M.26
168.5
28.99
249.0
28.15
-
3.3
0.05
6.5
0.41
20.3
1.20
202.0
31.03
1130.3
27.81
‘Arbat’/M.26
182.0
2.52
223.3
10.17
2.9
0.18
3.9
0.23
9.3
0.88
10.7
0.33
210.0
51.05
363.0
78.08
24217/M.26
173.3
6.98
212.0
10.07
2.7
0.11
3.6
0.14
14.3
0.67
26.3
2.33
264.3
8.84
411.7
51.28
‘Aldas’/P 60
212.3
5.93
268.7
3.93
-
3.3
0.09
10.0
2.31
27.0
0.58
208.3
40.60
1201.3
111.21
‘Arbat’/P 60
167.7
7.22
190.3
10.11
3.3
0.11
3.7
0.05
10.7
1.67
12.3
1.45
286.0
27.19
256.7
41.87
24217/P 60
145.7
5.21
168.0
4.62
2.7
0.11
3.3
0.11
10.0
1.16
24.3
4.33
217.3
36.98
318.7
31.39
* In numerator – trait value, in denominator – error / skaitiklyje – poþymio vertë, vardiklyje –
paklaida
In 2003 natural type habit cultivar ‘Aldas’ had the highest shoot number on
rootstock MM.106, columnar type habit cultivars No. 24217 and ‘Arbat’ had the highest
shoot number on rootstock M.26 and P 60, respectively. ‘Aldas’ had the highest shoot
number on all used rootstocks and ‘Arbat’ had the lowest shoot number in 2004.
Above mentioned apple cultivars had the same tendency for total shoot length.
The significant differences for total leaf area on a tree were estimated in 2003
(second growth season in an orchard) (Fig. 1). ‘Aldas’ had the lowest area of leaves
on all investigated rootstocks and the value of this trait was very close
(0.59–0.84 m2). Leaf area of columnar type apple cultivars was higher then it was
detected for ‘Aldas’. In 2004 ‘Aldas’ significantly differed for leaf area (3.79 m2)
only on rootstock MM.106. All cultivars had very close leaf area on rootstocks M.26
and P 60 in this year.
The lowest chlorophyll a content (1.06 mg/g) was detected for ‘Aldas’ on
rootstock MM.106 and it was significantly different from the content detected for
other cultivars (Fig. 2a). Influence on chlorophyll a content of rootstocks was not
detected. Significant differences were detected for chlorophyll b content for apple
cultivar ‘Arbat’ on M.26 and P 60. ‘Aldas’ had significantly low content of chlorophyll
b on all rootstocks (0.22 mg/g). No influence on chlorophyll b content of rootstocks
was detected. ‘Aldas’ grafted on MM.106 had significantly the lowest content of
352
carotenoids (0.54 mg/g) and the highest carotenoids content had ‘Arbat’ on P 60
(0.67 mg/g) (Fig. 2b). Rootstocks had no influence on chlorophyll b content in
leaves of ‘Arbat’ and No, 24217; it varied from 0.60 to 0.67 mg/g.
1
F i g. 1. Fruit tree total leaf area
p a v.
Vaismedþiø bendras lapø plotas
a
b
F i g. 2. Pigment content in apple leaves: a) chlorophyll, b) carotenoids
2
p a v.
Pigmentø kiekis obelø lapuose: a) chlorofilø, b) karotinoidø
353
The highest value of chlorophyll a and b content ratio was detected for cultivar
‘Aldas’ grafted on all investigated rootstocks (MM.106 – 4.90, M.26 – 4.90 and P 60
– 5.13) (Fig. 3). Ratio of chlorophyll a and b was for columnar type habit cultivars.
F i g. 3. Ratio of chlorophyll a and b
3
p a v. Chlorofilo a ir b santykis
The lowest photosynthesis was recorded in the leaves of ‘Aldas’ and its intensity
varied from 3.80 µmol/m2/s (rootstock M.26) to 4.80 µmol/m2/s (P 60) (Fig. 4).
Influence of rootstocks to photosynthesis was not detected. The highest
photosynthesis showed No. 24217 on rootstock MM.106 and P 60 (7.90 µmol/m2/s
and 7.64 µmol/m2/s), ‘Arbat’ – on M.26 (7.99 µmol/m2/s). Influence of rootstocks
on photosynthesis in leaves of columnar apple cultivars was significant.
F i g. 4. Photosynthesis activity in leaves of apple cultivars
4
p a v.
Fotosintezës aktyvumas ávairiø veisliø obelø lapuose
Discussion. Our results show that differences of tree height and trunk diameter
among observed columnar type apple trees and normal type trees are not extremely
big in the third year of vegetation and they correspond with results of other researches
354
(Inomata et al., 2004, 2005). Significant differences of shoot number and total length
were recorded among evaluated apple cultivars on rootstocks MM.106, M.26 and
P 60, but on the other hand the above-mentioned traits were influenced by rootstock
as well. Influence of rootstocks for tree leaf area was recorded only for ‘Aldas’. It
has significantly higher leaf area on a tree on rootstock MM.106 in both years of
study.
Chlorophyll a, b and carotenoids content in apple leaves were more influenced
by genotype than by rootstocks, except ‘Aldas’. The latter apple cultivar grafted on
rootstock MM.106 had significantly less leaf pigments. Photosynthesis intensity was
significantly lower in leaves of ‘Aldas’ than it was detected for columnar apple
cultivars, except ‘Arbat’ on P 60.
Conclusions. 1. Apple cultivar ‘Aldas’ with natural type habit is more vigorous
than columnar apple cultivars. Values of morphological traits of investigated cultivars,
in most cases, were higher on the semi-vigorous rootstock MM.106.
2. Natural type habit apple cultivar ‘Aldas’ grafted on rootstock MM.106 have
significantly the highest tree leaf area in the 3rd growth season in the orchard. Leaf
area of investigated cultivars on rootstocks M.26 and P 60 do not differ significantly.
3. Chlorophyll (a + b) and carotenoids content in leaves of ‘Aldas’ grafted on
rootstock MM.106 was significantly lower than it was recorded for columnar cultivars
on the same rootstock and other rootstocks as well. But chlorophyll a and b ratio
detected for ‘Aldas’ on all rootstocks was the highest.
4. Photosynthesis intensity of columnar apple cultivar is higher when it was
recorded for ‘Aldas’.
Gauta
2006 07 24
Parengta spausdinti
2006 07 31
References
1. I n o m a t a Y., K u d o K., M a s u d a T., B e s s h o H., W a d a
M. and S u z u k i K. Growth and fruit productivity habits of columnar type apple
selections // Horticultural research (Japan). 2004. 3(4): 392–401.
2. I n o m a t a Y., K u d o K., W a d a M., M a s u d a T., B e s s h o
H. and S u z u k i K. The influence of rootstock on characteristics of tree growth, fruit
productivity and dry matter production of ‘Maypole’ young apple tree // Horticultural
research (Japan). 2005. 4(1): 41–46.
3. K v i k l y s D. Apple rootstock research in Lithuania with aspect to quality and
tree productivity // Horticulture and vegetable growing. 2002. 21(3): 3–13.
4. M e l a n d M., F r o y n e s O., M o e M. E. Early performance of
‘Discovery’ apples on 8 rootstocks growing in a northern climate // Acta Horticulturae.
2004. No 658.
5. Q u i n l a n J. D., T o b u t t K. R. Manipulating fruit tree structure chemically
and genetically for improved performance // HortScience. 1990. 25(1): 60–63.
6. R o b i n s o n T. L., H o y i n g S. A. Performance of elite cornell Geneva
apple rootstocks in long-term orchard trials on growers farms // Acta Horticulturae. 2004.
No 658.
355
7. S a d o w s k i A., D z i u b a R., J a b l o n s k i j K. Growth and cropping
of three apple cultivars on different rootstocks over a 7-year period // Acta Horticulturae.
2004. No 658.
8. T a k a c s F. Performance of apple cultivars and rootstocks in various orchards
systems in north-eastern Hungary // Acta Horticulturae. 2004. No 658.
9. T o b u t t K. R. Breeding columnar apple at East Malling // Acta Horticulturae.
1985. 159: 63-68.
10. T o b u t t K. R. Breeding of apple and pears – Columnar apples // Annu. Rpt.
E. Malling Res. Sta. for 1985. 1986: 61.
11. W e t t s t e i n D. Chlorophyll Letale und der submikroskopishe
Formweschsel der Plastiden. Experimental cell research 12. 1957. 427 p.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
350–356.
MORFOLOGINËS IR FIZIOLOGINËS KOLONINIØ OBELØ VEISLIØ
SAVYBËS
B. Gelvonauskis, A. Brazaitytë, A. Sasnauskas, P. Duchovskis, D. Gelvonauskienë
Santrauka
Lietuvos sodininkystë ir darþininkystës instituto (LSDI) bandymø sode tirta obelø
koloninë veislë ‘Arbat‘, selekcinis numeris 24217 ir ‘Aldo‘veislë, kuriai bûdingas neutralus
vaismedþio vainikas. ’Aldas‘ ir Nr. 24217 sukurti LSDI, ’Arbat‘ – Rusijoje. Tirtø veisliø
vaismedþiai akiuoti á P 60, M.26 ir MM.106 poskiepius. Medeliai pasodinti sode 1,0 x 3,5 m
atstumais. Ávertintas vaismedþiø aukðtis, kamieno skersmuo, bendras ûgiø ilgis, ðakø
skaièius, lapø plotas. Nustatytas chlorofilø ir karotinoidø kiekis lapuose ir fotosintezës
aktyvumas.
Nustatyta, kad tirti þemaûgiai poskiepiai turëjo esminës átakos tirtø veisliø vaismedþiø
aukðèiui, kamieno skersmeniui, ðakø skaièiui, bendram ûgliø ilgiui. Maþiausiai augûs buvo
koloniniø veisliø medeliai su P 60 poskiepiu treèiaisiais augimo sode metais,’Aldo‘
veislës – su M.26 poskiepiu. ’Aldo‘ veislës medeliai iðaugino daugiausia ðakø, jø bendras
ûgliø ilgis buvo didþiausias. Su MM.106 poskiepiu augintø visø tirtø veisliø vaismedþiø
rodikliai buvo geriausi. Didþiausias lapø plotas buvo su MM.106 poskiepiu augintø ’Aldo‘
veislës medeliø ir su M.26 ir P 60 poskiepiais auginto selekcinio numerio 24217. Chlorofilø
a ir b kiekis ’Aldo‘ veislës obelø lapuose buvo maþiausias, auginant su visais poskiepiais.
Esminiai karotinoidø kiekio ávairiø veisliø obelø lapuose skirtumai gauti vaismedþius
auginant su P 60 poskiepiu. Poskiepiai turëjo átakos jø kiekiui tik ’Aldo‘ veislës lapuose.
Aktyviausia fotosintezë vyko Nr. 24217, auginto su MM.106 ir P 60 poskiepiais, ir ’Arbat‘
veislës, augintos su M.26 poskiepiu, lapuose.
Reikðminiai þodþiai: karotiniodai, chlorofilas, fotosintezë, poskiepiai, vaismedþiø
augimas.
356
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 357–363.
ROOTSTOCK EFFECT ON PHOTOSYNTHETIC PIGMENT
SYSTEM FORMATION IN LEAVES OF APPLE
CV. ‘AUKSIS’
Gintarë ÐABAJEVIENË, Darius KVIKLYS,
Pavelas DUCHOVSKIS
Lithuanian Institute of Horticulture, LT–54333 Babtai, 54333 Kaunas distr.,
Lithuania. E-mail: [email protected]
Photosynthetic pigment system in the leaves of apple tree cv. ‘Auksis’ on different
rootstocks was investigated at the Lithuanian Institute of Horticulture during 2003–2005.
Twelve rootstocks were included: Bulboga, Pure1, York 9, B.9, B.396, B.416, B.491, M.9,
M.26, P 2, P 60, P 22. The photosynthetic pigment content and ratios of apple tree cv.
‘Auksis’ on different rootstocks varied between years. Photosynthetic pigment content
and chlorophyll a/b ratio in apple leaves depend on crop load: the higher crop the higher
photosynthetic pigment content and lower chlorophyll a/b ratio. Rootstock genotype
determines accumulation of photosynthetic pigments. Apple rootstocks M.9 and York 9
accumulate larger amount of total chlorophyll and carotenoid content than M.26. In average
lower chlorophyll a/b ratio was established for apple trees on P 22, higher ratio – on
rootstocks P 60, B.9 and B.146.
Key words: chlorophyll, carotenoid, Malus x domestica, rootstock.
Introduction. The importance of rootstocks is more and more widely
recognised, which, in terms of their influence on yield productivity, are not less
important than the grafted scions. Various apple rootstocks, as inhibitors or stimulators,
can influence growth, fruiting initiation, crop, fruit quality and other biological and
economical properties.
The content of chlorophylls and carotenoids, the main pigments of leaf, provides
valuable information about plant physiological status. Chlorophylls are virtually
essential pigments for the conversion of light energy to stored chemical energy. The
amount of solar radiation absorbed by a leaf is a function of the photosynthetic
pigment content; thus, chlorophyll content can directly determine photosynthetic
potential and primary production (Curran et al., 1990; Filella et al., 1995). Chlorophyll
gives an indirect estimation of the nutrient status because much of leaf nitrogen is
incorporated in chlorophyll (Filella et al., 1995; Moran et al., 2000). Furthermore,
leaf chlorophyll content is closely related to plant stress and senescence (Merzlyak,
Gitelson 1995; Merzlyak et al., 1999). Rootstock effect on chlorophyll content was
detected for various fruit species (Cinelli et al., 2004; Muleo et al., 2002).
357
The changes of leaf carotenoids content and their proportion to chlorophyll are
widely used for diagnosing the physiological state of plants during development,
senescence, acclimation and adaptation to different environments and stresses
(Demmig-Adams et al., 1996).
The aim was to study apple rootstock effect on photosynthetic pigment system
formation in leaves of apple cv. ‘Auksis’.
Materials and methods. Research was carried out with cultivar ‘Auksis’ on
twelve rootstocks (Bulboga, Pure1, York 9, B.9, B.396, 57-416, B.491, M.9, M.26,
P 2, P 60, P 22). The orchard was planted in the spring of 2001. Planting distances
were 4x1.5 m. Trees were trained as slender spindles. The trial consisted of four
replications with 3 trees in each. Replications were randomised.
The measurements of chlorophyll were performed on 3 plants from each variant.
Samples were taken in August. The fourth fully developed leaf from the east side of
the tree was taken for chlorophyll and carotenoid extraction in 100% acetone and
evaluation by the spectrophotometric method according to Weittstein (Ãàâðèëåíêî,
2003). The concentrations of pigments were detected by Spectrophotometer –
Genesys 6 (ThermoSpectronic, USA).
Variance analysis was done with a Duncan’s Multiple Range t-test (P≤0.05)
using the ‘ANOVA’ statistical program.
According growth vigour control all tested rootstocks were grouped in the
following way: less vigorous than M.9 – P 22, the same as M.9 – Pure 1, B.396,
York 9, P.60, B.9 and P 2, between M.9 and M.26 – B.491, the same or more
vigorous as M.26 – Bulboga and B.146.
Due to spring frost in 2004 the average yield per tree was low – 4–10 kg, when
in 2005 the average yield varied from 13 to 24 kg/tree.
Results. Contents and ratios of the photosynthetic pigments in apple tree cv.
‘Auksis’ on different rootstocks varied between years. The largest amounts of
chlorophylls and carotenoids in 2003 were accumulated leaves of apple trees on
Bulboga (chlorophylls a + b content 2.052 mg g-1, carotenoids – 0.602 mg g-1) and
B.396 (chlorophylls a + b content 1.982 mg g-1, carotenoids – 0.573 mg g-1) rootstocks
(Table 1. and Table 2), though significant differences were established only on Bulboga
rootstock. The smallest amount of chlorophylls was determined in leaves of ‘Auksis’
on rootstock B.9 (1.410 mg g-1). Lower content of carotenoids was in trees on
rootstocks P 60, and B.9 (about 0.45 mg g-1), though there were significant differences
only with trees on rootstock Bulboga. Significantly smaller amounts of chlorophylls
and carotenoids in apple trees leaves were accumulated in 2004. The largest content
of photosynthetic pigments was found in apple trees on rootstocks P 22, P 2 and
B.396 (total chlorophylls content was about 1.18 mg g-1, carotenoids – 0.38 mg g-1).
Fruit trees ‘Auksis’ on rootstock Bulboga accumulated the smallest amount of
chlorophylls (0.735 mg g-1), and carotenoids (0.251 mg g-1). In 2005 the amount of
chlorophylls in apple tree leaves ranged from 1.881mg g-1 to 2.115 mg g-1. Significantly
higher chlorophyll contents were in combinations ‘Auksis’ on rootstock York 9
(2.614 mg g-1). Apple cv. ‘Auksis’ on rootstock M.9 accumulated high amount of
chlorophyll too (2.326 mg g-1). Larger amounts of carotenoids accumulated apple
trees on rootstock B.146 (0.642 mg g-1).
358
T a b l e 1. Chlorophyll content in leaves of apple tree cv. ‘Auksis’ on
different rootstocks, mg g-1
1
l e n t e l ë.
Rootstock
Chlorofilo kiekis ‘Auksio’ veislës obelø su skirtingais poskiepiais
lapuose, mg g-1
Chlorophyll a content
Chlorophyll a + b content /
Chlorofilo a kiekis
Chlorofilo a + b kiekis
Average
Poskiepis
2003
2004
2005
Average
2003
Vidurkis
2004
2005
2003–2005
Bulboga 1.577c 0.564a 1.507ab
P 22
1.383ab 0.904d 1.383a
1.216
1.223
M.26
1.217ab 0.651ab 1.392ab
P2
P 60
York 9
1.287ab 0.915d 1.595abc
1.242ab 0.854cd 1.564abc
1.317ab 0.764bcd 1.941c
M.9
Vidurkis
2003–2005
2.052b
1.803ab
0.735a
1.195e
2.003ab
2.068ab
1.641
1.689
1.087
1.585ab
0.835abc
1.881a
1.434
1.266
1.219
1.341
1.680abc
1.178de 2.115ab
1.598ab
1.08cde 2.098ab
1.713ab 0.952abcde 2.614c
1.658
1.592
1.760
1.394ab 0.762bcd 1.733bc
1.296
1.803ab
0.971abcde 2.326bc
1.700
Pure 1
B.9
B.396
B.146
1.198ab
1.099a
1.509ab
1.13ab
0.883cd 1.512ab
0.858cd 1.466ab
0.817bcd 1.456ab
0.677abc 1.564abc
1.198
1.278
1.261
1.124
1.539abc
1.410a
1.982ab
1.471ab
1.156de
1.092cde
1.032bcde
0.799ab
2.052ab
1.970ab
1.939ab
2.077ab
1.582
1.491
1.651
1.449
B.491
1.237ab 0.634ab 1.564abc
1.145
1.603ab
0.861abcd 2.072ab
1.512
Values followed by the same letters within the columns are not statistically different at P≤0.05.
Tomis paèiomis raidëmis skiltyse paþymëti skaièiai ið esmës nesiskiria (P≤0,05).
T a b l e 2. Carotenoids content in leaves of apple tree cv. ‘Auksis’ on
different rootstocks, mg g-1
2
l e n t e l ë. Karotinoidø kiekis ‘Auksio’ veislës obelø su skirtingais poskiepiais
lapuose, mg g-1
Rootstock
Poskiepis
Carotenoids content / Karotinoidø kiekis
2003
2004
2005
Average / Vidurkis
2003–2005
Bulboga
0.602b
0.251a
0.524abc
0.459
P 22
M.26
0.520ab
0.481ab
0.378cd
0.310ab
0.409a
0.496ab
0.436
0.429
P2
0.515ab
0.394d
0.563bc
0.491
P 60
York 9
M.9
Pure1
0.446a
0.505ab
0.541ab
0.471ab
0.379cd
0.352bcd
0.342bcd
0.375cd
0.560bc
0.642c
0.577bc
0.535abc
0.462
0.500
0.487
0.460
B.9
B.396
0.440a
0.573ab
0.365bcd
0.380cd
0.523abc
0.503abc
0.443
0.485
B.146
0.451ab
0.318bc
0.602bc
0.457
B.491
0.470ab
0.325bc
0.548bc
0.448
Values followed by the same letters within the columns are not statistically different at P≤0.05.
Tomis paèiomis raidëmis skiltyse paþymëti skaièiai ið esmës nesiskiria (P≤0,05).
359
In 2003 and 2004 chlorophyll a/b ratio varied from 3.164 to 3.534 (Table 3.)
The highest efficiency of photosynthesis was in 2004. Chlorophyll a/b ratio varied
from 3.291 to 3.837. Significantly lower chlorophyll a and chlorophyll b ratios in
apple tree leaves were determined in 2005 (from 2.802 to 3.07), especially on rootstock
P 22 that differed significantly from all tested rootstocks.
T a b l e 3. Chlorophyll a/b ratio in leaves of apple tree cv. ‘Auksis’
on different rootstocks
3
l e n t e l ë. Chlorofilo a ir b santykis ‘Auksio’ veislës obelø su skirtingais
poskiepiais lapuose
Rootstock / Poskiepis
2003
2004
2005
Average / Vidurkis 2003–2005
Bulboga
3.315abc
3.608abc
3.036bc
3.320
P 22
3.321abc
3.291a
2.073a
2.895
M.26
3.305abc
3.544abc
2.845bc
3.231
P2
3.405abc
3.511abc
3.070bc
3.329
P 60
3.475bc
3.787bc
2.937bc
3.400
York 9
3.344abc
3.492abc
2.883bc
3.240
M.9
3.377abc
3.690abc
2.918bc
3.328
Pure1
3.521bc
3.266a
2.802bc
3.196
B.9
3.534c
3.694abc
2.931bc
3.386
B.396
3.164a
3.837c
3.020bc
3.340
B.146
3.329abc
3.793bc
3.029bc
3.384
B.491
3.344abc
3.667abc
3.07c
3.360
Values followed by the same letters within the columns are not statistically different at P≤0.05.
Tomis paèiomis raidëmis skiltyse paþymëti skaièiai ið esmës nesiskiria (P≤0,05).
Discussion. The photosynthetic pigment content in apple tree cv. ‘Auksis’ on
different rootstocks varied between years. The lowest chlorophyll and carotenoid
content was observed in 2004 when significant part of the yield was lost because of
spring frosts. The highest amount of photosynthetic pigments was detected in 2005
when abundant yield was collected on all tested rootstocks. Dependence of crop
load on photochemical yield was shown in others trials too (Greer et al., 1997).
Apple tree productivity is determined by many parameters, such as chlorophyll
content in leaves, carotenoid content, etc., as they are indicators of physiological
activity in leaves (Curran et al., 1990; Filella et al., 1995). Leaf pigment content
provides valuable information about the physiological status of plants. Apple
cv. ‘Auksis’ stored larger amount of photosynthetic pigments on rootstocks York 9
and M.9 that show medium growth vigour and optimal productivity. Fruit trees on
rootstocks M.26 and B.146 accumulated the smallest content of chlorophylls and
they were distinguished for stronger vegetative growth in tested rootstock group.
360
Exception was trees on rootstock Bulboga that exhibited the strongest growth and
were at least productive but accumulated high contents of chlorophylls and
carotenoids. Rootstock genotype coursed differences were detected with other fruit
tree species too. A decrease of chlorophyll was less on GF677 than those grafted on
Mr.S.2/5 (Cinelli et al., 2004). Mineral nutrient deficiency decreased total chlorophyll
content in pear rootstock MA in comparison with others (Muleo et al., 2002).
Carotenoids take active part in photosynthesis. The level of carotenoids changes
during vegetative growth (Demmig-Adams, Adams, 1996). The largest amount of
carotenoids was found in fruit trees on rootstocks York 9, P 2, M.9 and B.396. In
the period of investigation the lowest level of carotenoids produced apple tree leaves
on rootstock M.26.
Chlorophyll a and chlorophyll b ratio is substantial photosynthetic activity
indicator (Datt, 1998). In the period of investigation the highest efficiency of
photosynthesis was in apple tree leaves grafted on rootstocks P 60 and B.146. The
lowest chlorophyll a/b ratio was determined in apple tree leaves on rootstocks P 22
and Pure 1. Both rootstocks were the most dwarfing and the most productive in the
tested rootstock group, but decreased apple fruit weight significantly.
Chlorophyll ratio, as well as photosynthetic pigment content, varied between
years and depended on crop load. Chlorophyll a/b ratio decreased in 2005 when
trees on all rootstocks gave very high yield, and was higher in 2004 when trees were
not so productive. Nevertheless, during research the ratio of chlorophyll a and
chlorophyll b in all analysed apple tree leaves varied about 3 and didn’t limit
photosynthesis.
Conclusions. 1. Rootstock genotype determines accumulation of photosynthetic
pigments. Apple rootstocks M.9 and York 9 accumulate larger and M.26 smaller
amounts of total chlorophyll and carotenoid content.
Significant differences between rootstocks in chlorophyll a/b ratio varied between
years. In average lower ratio was established for apple trees on P 22, higher ratio –
on rootstocks P 60, B.9 and B.146.
Photosynthetic pigment content and chlorophyll a/b ratio in apple leaves depends
on crop load: the higher the crop the higher photosynthetic pigment content and
lower chlorophyll a/b ratio.
Acknowledgement. This work was partly supported by Lithuanian State Science
and Studies Foundation.
Gauta
2006 07 14
Parengta spausdinti
2006 8 08
361
References
1. C i n e l l i F. T a m a n t i n i I., I a c o n a C. Nutritional (Fe-Mn)
interactions in “Big Top” peach plant as influenced by the rootstock and by the soil
CaCO3 concentration // Soil science and plant nutrition. 2004. 50 (7): 1097–1102.
2. C u r r a n P. J. D u n g a n J. L., G h o l z H. L. Exploring the relationship
between reflectance red edge and chlorophyll content in slash pine // Tree Physiol. 1990.
Vol. 7. P. 33–48.
3. D a t t B. Remote Sensing of Chlorophyll a, Chlorophyll b, Chlorophyll a + b,
and Total Carotenoid Content in Eucalyptus Leaves // Remote Sens. Environ. 1998. Vol.
66. P. 111–121.
4. D e m m i g - A d a m s B., A d a m s W. W. The role of xanthophylls cycle
carotenoids in the protection of photosynthesis // Trends in plant science. 1996. Vol. 1.
No. 1. P. 62–73.
5. G r e e r, D. H., W ü n s c h e, J. N. P a l m e r, J. W. Effects of fruiting on
seasonal apple leaf chlorophyll fluorescence //Acta Horticulturae,1997. 451:345–350.
6. Filella I., Serrano I., Serra J., Peuelas J. Evaluating wheat nitrogen status with
canopy reflectance indices and discriminant analysis // Crop Sci 1995. Vol. 35. P. 1400–
1405 .
7. M e r z l y a k M. N., G i t e l s o n A. A. Why and what for the leaves are
yellow in autumn? On the interpretation of optical spectra of senescing leaves (Acer
platanoides L.)// Plant Physiol 1995. Vol. 145. P. 315–320.
8. M e r z l y a k M. N., G i t e l s o n A. A., C h i v k u n o v a O. B.,
R a k i t i n V. Y. Nondestructive optical detection of leaf senescence and fruit ripening
// Physiol Plant. 1999. Vol. 106. P. 135–141.
9. M o r a n J. A., M i t c h e l l A. K., G o o d m a n s o n G.,
S t o c k b u r g e r K. A. Differentiation among effects of nitrogen fertilization
treatments on conifer seedlings by foliar reflectance: a comparison of methods. // Tree
Physiol. 2000. Vol. 20. P. 1113–1120.
10. M u l e o R., F i s i c h e l l a M., I a c o n a C., V i t i R., C i n e l l i
F. Different responses induced by bicarbonate and iron deficiency on microshoots of
quince and pear // Acta Horticulturae. 2002. 596: 677–681.
11. Ã à â ð è ë å í ê î Â. Ô., Ë à ä û ã è í à Ì. Å., Õ à í ä ð î á è í à
Ë. Ì. Áîëüøîé ïðàêòèêóì ïî ôèçèîëîãèè ðàñòåíèé. Ìîñêâà, Aêaäåìèÿ,
2003. 256 c.
362
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
357–363.
POSKIEPIØ ÁTAKA ‘AUKSIO’ VEISLËS OBELØ FOTOSINTETINIØ
PIGMENTØ SISTEMAI
G. Ðabajevienë, D. Kviklys, P. Duchovskis
Santrauka
Fotosintetiniø pigmentø obelø lapuose sistemos tyrimai atlikti 2003–2005 m. Lietuvos
sodininkystës ir darþininkystës institute. Tirtos ‘Auksio’ veislës obelys su 12 poskiepiø:
Bulboga, Pure1, York 9, B.9, B.396, B.416, B.491, M.9, M.26, P 2, P 60, P 22. Bandymo
laikotarpiu fotosintetiniø pigmentø kiekiai ir jø santykis kito. Obelims gausiai derant,
bendras fotosintetiniø pigmentø kiekis lapuose buvo didesnis, jø santykis – maþesnis.
Fotosintetiniø pigmentø kiekis lapuose priklausë nuo obelø poskiepiø: daugiau chlorofilo
ir karotinoidø kaupë obelys su M.9 ir York 9 poskiepiais, maþiau – su M.26 poskiepiu.
Maþesnis chlorofilo a ir chlorofilo b santykis nustatytas obelø su P 22, didesnis – su P 60,
B.9 ir B.146 poskiepiais lapuose.
Reikðminiai þodþiai: chlorofilas, karotinoidai, Malus x domestica, poskiepis.
363
SCIENTIFIC WORKS OF THE LITHUANIAN INSTITUTE OF
HORTICULTURE AND LITHUANIAN UNIVERSITY OF AGRICULTURE.
SODININKYSTË IR DARÞININKYSTË. 2006. 25(3). 364–370.
CHLOROPHYLL FLUORESCENCE CHARACTERISTICS
OF CULTIVAR ‘AUKSIS’ ON ROOTSTOCKS P 22 AND
P 60 IN HIGH DENSITY ORCHARDS OF DIFFERENT
CONSTRUCTION
Gintarë ÐABAJEVIENË1, Jurga SAKALAUSKAITË1,
Vytautas ÐLAPAKAUSKAS2, Nobertas USELIS1,
Pavelas DUCHOVSKIS1
1
Lithuanian Institute of Horticulture, LT–54333 Babtai, Kauno 30,
Kaunas distr., Lithuania. E-mail: [email protected]
Lithuanian University of Agriculture, LT–53067 Akademija, Studentø 11,
Kaunas distr., Lithuania
2
Fluorescence parameters in apple tree leaves of cv. ‘Auksis’ on rootstocks P 60 and
P 22 were investigated at the Lithuanian Institute of Horticulture in 2005. Apple trees were
trained as spindle, slender spindle, slender spindle V form, free leader axis, super spindle
and super spindle V form. Orchards on rootstock P 60 were planted using 3 x 1.5 m;
3 x 1.25 m; 3 x 1 m and 3 x 0.75 m planting scheme, apple trees on P 22 – 3 x 1 m; 3 x 0.75 m;
3 x 0.5 m and 3 x 0.25 m. planting scheme. A fall in fluorescence parameters due to the
higher planting density proves that the researched fruit trees experienced stress. However,
with every further enlargement of planting density, the mentioned parameters were changing
positively. That enables to conclude that the examined apple trees experienced competitive
stress. Distinct fluorescence parameters of different rootstocks show that the response
of the fruit tree within inter-competition depends on the rootstock type. The open tree
forms allow optimum light interception. This feature determinates high photochemical
efficiency in leaves. The highest quantum yield and electron transport were detected in
super spindle V form and slender spindle V form apple trees.
Key words: apple tree, density, electron transport rate, maximum fluorescence,
minimum fluorescence, quantum yield, rootstock, tree form.
Introduction. Since the late 1980’s there has been a rapid increase in planting
density of apple trees in different regions of Europe (Mantinger and Vigl, 1999).
About ten years later, Widmer and Lemmenmeier (1999) showed that the highest
yield was in orchards with 10 000 trees per ha. The planting system and tree form is
crucial for growth, productivity, yield and fruit quality in apple orchard (Uselis,
2003).
364
Different kinds of fruit trees request specific physiological conditions for their
growth and development. Aberration from optimal conditions can lead to a stress.
Investigations of other scientist groups demonstrated that fruit tree density influences
crop yield and fruit quality (Stampar et al., 1998). With increase of planting density,
productivity per tree decreases, whereas cumulative productivity per hectare increases
(Jackson et al., 1981; Mika and Piàtkowski, 1986). Training and formation of fruit
tree directly and indirectly affects the size of assimilation area, as well as the intensity
of photosynthesis. The importance of rootstocks is more and more widely recognised,
which, in terms of their influence on crop productivity, are not less important than
the grafted scions.
Fluorescence is proved to be especially effective for quantifying the effects of
environmental stress, such as drought, light stress, extreme temperature, nutrient
deficiency or pollution, on plant function (Jackson, 1986; Carter, 1991, 1993, 1994;
Aldakheel and Danson, 1997). This can be directly related to the overall efficiency or
health of a leaf’s photochemical apparatus, which is impaired by stress (Krause and
Weis, 1991; Ball et al., 1994). Damage caused by photoinhibition may be assessed
by determining fluorescence and emission through chlorophyll a in plants treated
with strong irradiation pulses. By measuring the emission of fluorescence, it has
been found that photoinhibition is mainly observed in photosystem II (PS II) (Krause
and Weis, 1991). This non-destructive technique has been a common approach for
estimating PS II efficiency. Fluorescence indexes used for evaluating PS II functioning
include: initial fluorescence (Fo), maximum fluorescence (Fm) variable fluorescence
(Fv) and Fv/Fm ratio (Shole and Horton, 1993). Fv represents the difference between
Fm and Fo (Fv = Fm-Fo). The Fo parameter is the minimal fluorescence yielded
when all reaction centres are in the oxidized or open state. When leaves are briefly
exposed to a saturating light level, all PS II centres are closed. That is, quinone A
(QA) is reduced and a maximum yield of fluorescence (Fm) is observed. The Fv/Fm
ratio, calculated as Fv/Fm=(Fm-Fo)/Fm, is a fluorescence variable directly correlated
with the physiological efficiency of the photosynthetic machinery. This ratio is been
considered to be proportional to the quantum efficiency of PS II (Bjorkman and
Demming, 1987). In a wide number of plant species and ecotypes, an Fv/Fm ratio of
0.83 has been obtained in unstressed leaves. Hence, the effects of stressful
environmental factors on PS II may be examined by determining the reduction in the
Fv/Fm ratio (Ogren and Evans, 1992; Sholes and Horton, 1993). The yield parameter
corresponds to Fv/Fm, but its value generally is lower than Fv/Fm.
The aim of this study was to determine chlorophyll fluorescence effect in apple
tree with different rootstock leaves on different planting densities and training systems.
Materials and methods. Research was carried out with cultivar ‘Auksis’ on
rootstocks P60 and P22 at the Lithuanian Institute of Horticulture in 2005.
Planting scheme of apple trees cv. ‘Auksis’ with rootstock P 60: 1 – spindle
training system, planting density – 3 x 1.5 m (2222 trees per ha); 2 – slender spindle
training system, planting density – 3 x 1.5 m (2222 trees per ha); 3 – free leader axis
training system, planting density – 3 x 1.5 m (2222 trees per ha); 4 – spindle training
system, planting density – 3 x 1.25 m (2667 trees per ha); 5 – slender spindle training
system, planting density – 3 x 1.25 m (4444 trees per ha); 6 - spindle training system,
365
planting density – 3 x 1 m (3333 trees per ha); 7- slender spindle training system,
planting density – 3 x 1 m (3333 trees per ha); 8 – super spindle training system,
planting density – 3 x 0.75 m (4444 trees per ha); 9 – slender spindle training system,
planting density – 3 x 0.75 m (4444 trees per ha).
Planting scheme of apple tree cv. ‘Auksis’ on rootstock P 22: 1- spindle training
system, planting density – 3 x 1 m (3333 trees per ha); 2 – slender spindle training
system, planting density – 3 x 1 m; (3333 trees per ha); 3 – free leader axis training
system, planting density – 3 x 1 m (3333 trees per ha); 4 – super spindle training
system, planting density – 3 x 0.75 m (4444 trees per ha); 5 – slender spindle training
system, planting density – 3 x 0.75 m (4444 trees per ha); 6 - spindle training system,
planting density – 3 x 0.5 m (6667 trees per ha); 7- super spindle V form training
system, planting density – 3 x 0.5 m (6667 trees per ha); 8 – slender spindle V form
training system, planting density – 3 x 0.25 m (13333 trees per ha); 9 – super spindle
training system, planting density – 3 x 0.25 m (13333 trees per ha); 10 - super
spindle V form training system, planting density – 3 x 0.25 m (13333 trees per ha).
The measurements were performed on 5 plants from each apple tree cultivar.
The fourth fully developed leaf from the east side of the tree was taken for analysis.
The fluorescence was measured by a chlorophyll fluorometer PAM-210, Walz GmBH.
The minimum (actual) fluorescence yield in light adapted sample (Ft) and maximum
fluorescence yield (Fm) of illuminated light-adapted sample were measured with
every saturation pulse 3500 µmol m-2s-1. Ft corresponds to the momentary value of
fluorescence yield at a given actinic light intensity (85 µmol m-2s-1). Fm is defined as
the maximum fluorescence yield of an illuminated sample induced by a saturation
pulse. The maximum light-acclimated photochemical quantum yield of PSII (Y) was
estimated according to the relationship Y= (Fm’-Ft) : Fm’ = ÄF : Fm’ and the electron
transport rate ETR = c x 0.5 x PAR x Y (Schreiber, 1995). Using this equation, it is
assumed that 84% of the incident quanta are absorbed and 50% of the absorbed
quanta are distributed to PS II.
Statistical calculations were performed by ANOVA for MS Excel vers. 3.43
(Duncan’s Multiple Range t-test procedure, P≤0.05).
Results. The variation of investigated fluorescence parameters was determined
by variable planting densities, tree forms and rootstocks.
Leaves of ‘Auksis’/P 22 with spindle form were distinguished for substantially
high minimum fluorescence (Ft) (Table 1). The most extensive Ft in super spindle
form fruit trees was estimated in 3x1 m. planting system. Ft level notably dropped
with reduction of orchard density. However, in case of highest density of fruit trees,
Ft increased in super spindle and super spindle V forms apple tree leaves. With
increase of planting density the level of minimum fluorescence of ‘Auksis’/P 22 fruit
trees with slender spindle fell down. The same tendencies were recognized in variations
of maximum fluorescence (Fm). Differences were seen just in super spindle V form
apple tree leaves, where Fm declined with growth of density of apple trees.
The quantum yield (Y) and rate of electron transport (ETR) in all kind of apple
tree forms fell down with decrease of planting density. The most intensive quantum
yield and electron transport were detected in super spindle V form apple tree leaves.
366
T a b l e 1. Chlorophyll fluorescence parameters in leaves of apple
tree cv. ‘Auksis’ on rootstock P 22
1
l e n t e l ë. Chlorofilø fluorescencijos rodikliai ‘Auksio’ veislës obelø su P 22
poskiepiu lapuose
Fluorescence parameters
Different canopy form and densities
combinations
Fluorescencijos rodikliai
Skirtingi vainiko formos ir tankumo deriniai
Ft
Fm'
Y
ETR
Spindle / Paprastoji verpstë, 3 x 1 m
Slender spindle / Laiboji verpstë, 3 x 1 m
Free leader axis / Laisvai augantis lyderinis vainikas,
3x1m
Super spindle / Superverpstë, 3 x 0,75 m
0,230c*
0,171ab
0,625bcd
0,597abcd
0,635a
0,710abc
16a
17,93ab
0,164ab
0,560abcd
0,697abc
17,55ab
0,180abc
0,618bcd
0,719bc
17,6ab
Slender spindle / Laiboji verpstë, 3 x 0,75 m
0,1985bc
0,693d
0,705abc
17,78ab
Super spindle / Superverpstë, 3 x 0,5 m
0,147a
0,401a
0,653abc 16,44ab
Super spindle V form / V formos superverpstë,
0,156ab 0,607abcd
0,738c
18,6b
3 x 0,5 m
Slender spindle V form / V formos laiboji verpstë,
0,16ab
0,498abcd 0,680abc 17,175ab
3 x 0,25 m
Super spindle / Superverpstë, 3 x 0,25 m
0,155ab
0,463ab
0,655abc 16,5ab
Super spindle V form / V formos superverpstë,
0,164ab 0,549abcd 0,694abc 17,48ab
3 x 0,25 m
*Values, indicated by the same letters within the columns, are not statistically different at P≤0.05.
*Tomis paèiomis raidëmis skiltyse paþymëti skaièiai ið esmës nesiskiria (P≤0,05).
T a b l e 2. Chlorophyll fluorescence parameters in leaves of apple
tree cv. ‘Auksis’ on rootstock P 60
2
l e n t e l ë. Chlorofilø fluorescencijos rodikliai ‘Auksio’ veislës obelø su P 60
poskiepiu lapuose
Fluorescence parameters
Different canopy form and densities
combinations
Fluorescencijos rodikliai
Skirtingi vainiko formos ir tankumo deriniai
Ft
Fm'
Spindle / Paprastoji verpstë, 3 x 1,5 m
Slender spindle / Laiboji verpstë,3 x 1,5 m
Free leader axis / Laisvai augantis lyderinis vainikas,
3 x 1,5 m
Spindle / Paprastoji verpstë, 3 x 1,25 m
Slender spindle / Laiboji verpstë, 3 x 1,25 m
0,173ab*
0,184ab
0,504abc
0,585c
0,167ab
0,458 a
0,636abc
16ab
0,166ab
0,164ab
0,503ab
0,56b
0,559a
0,710bc
16,775abc
17,773bc
Spindle / Paprastoji verpstë, 3 x 1 m
0,163ab
0,53ab
0,704bc
17,75bc
Slender spindle / Laiboji verpstë, 3 x 1 m
Super spindle / Superverpstë, 3 x 0,75 m
0,172ab
0,1855b
0,555ab
0,500ab
0,691abc 17,425abc
0,624abc 15,725a
Slender spindle / Laiboji verpstë, 3 x 0,75 m
0,163ab
0,579bc
Y
ETR
0,659abc 16,6abc
0,652abc 16,375abc
0,719c
18,1c
*Values, indicated by the same letters within the columns, are not statistically different at P≤0.05.
*Tomis paèiomis raidëmis skiltyse paþymëti skaièiai ið esmës nesiskiria (P≤0,05).
367
Dissimilar results were in orchards on rootstock P 60. The minimum fluorescence
in all apple tree forms declined with decrease of planting density. Highest Ft level
was found in fruit trees with super spindle form. Largest Fm in spindle and slender
spindle forms of fruit trees was detected in 3x1.5 m. planting system. Maximum
fluorescence dropped with reduction of orchard density.
The quantum yield (Y) and rate of electron transport (ETR) in all apple tree
forms fell down with decrease of planting density. However, when the fruit trees
were planted most densely, the quantum yield and rate of electron transport in apple
tree leaves increased. Highest rates of quantum yield and electron transport were
detected in slender spindle apple tree leaves.
Discussion. In the reports of other researches it has been noticed, that the size
of the productivity taken from one measurement was directly determined by the
number of fruit trees, however, only to the corresponding bounds (Jackson et al.,
1981; Mika, Pi¹tkowski, 1986). When the critical level was achieved, the intensity of
photosynthesis in leaves dropped due to the effect of shadowing, made by the plants
situated around (Wertheim et al., 1986). Correct orchard density and its appropriate
care are needed in order to assure enough quantity and distribution of light (Stampar
et al., 1998; Widmer, Krebs, 2001; Uselis, 2003).
Chlorophyll fluorescence analysis is a technique that provides information on
the functioning and the adaptation of the photosynthetic apparatus to the different
environmental conditions. The kinetics of chlorophyll fluorescence and the quantum
yield are known to be indicative of the electron flow in photosystem II (PS II). This
can be directly related to the overall efficiency or health of a leaf’s photochemical
apparatus, which is impaired by stress (Krause and Weis, 1991; Ball et al., 1994).
The quantum yield parameter reflects the efficiency of PS II. ETR factor defines the
fraction of incident light to be absorbed by the sample. Falling down of fluorescence
parameters, which was due to the higher planting density, proves that the researched
fruit trees experienced stress. It has been noticed in other studies as well, that enhanced
competition concerning densities acts as a minor stress for photosynthetic system
(Ðabajevienë et al., 2005 and Ðabajevienë et al., 2006). However, with every further
enlargement of planting density the mentioned parameters were changing positively.
That enables to conclude that the examined apple trees (‘Auksis’/P 22 and
‘Auksis’/P 60) experienced competitive stress.
Observed parameters of different rootstocks have been affected in a different
way as well: growth of density positively influenced Ft and Fm in leaves of apple
tree on rootstock P 22, and Y and ETR in leaves of apple tree on rootstock P 60. It
shows that the fruit tree response within inter-competition depends on the type of
rootstock.
The highest quantum yield and electron transport were detected in apple trees
of super spindle V form and slender spindle V form. The open forms allow optimum
light interception. This feature determines high photochemical efficiency in leaves.
In the researches of other groups of scientists it has been established that the open
forms with slender elements allow optimum light interception and generate good
yields with high fruit quality (Widmer and Krebs, 2001).
368
Conclusions. 1. A fall down in fluorescence parameters due to the higher planting
density proves that the investigated fruit trees experienced stress. The mentioned
parameters were changing positively with every further enlargement of planting
density. The examined apple trees (‘Auksis’/P 22 and ‘Auksis’/P 60) experienced
competitive stress.
2. Distinct fluorescence parameters of different rootstocks show that the
response of the fruit tree within inter-competition depends on the rootstock type.
3. The highest quantum yield and electron transport were detected in apple
trees of super spindle V form and slender spindle V form.
Gauta
2006 07 17
Parengta spausdinti
2006 08 07
References
1. A l d a k h e e l Y. Y., D a n s o n F. M. Spectral reflectance of dehydrating
leaves: measurements and modelling// Int. J. RemoteSens. 1997. Vol.18. P. 3683–3690.
2. Jackson, R.D. Remote sensing of biotic and abiotic plant stress // Annu. Rev.
Phytopathol. 1986. Vol. 24. P. 265–287.
3. J a c k s o n J. F., P e r r y M. S., S t e p h e n s C. P. Intensification of
tree fruit production: invent constrains, relevant research and an alternative system strategy
for the 1980 // Acta Hort. 1981. Vol. 114. P. 399–406.
4. B a l l M. C., B u t t e r w o r t h J. A., R o d e n J. S., C h r i s t i a n
R. E g e r t o n J. J. G. Applications of chlorophyll fluorescence to forest ecology //
Aust. J. Plant Physiol. 1994. Vol. 22. P. 311–319.
5. B j o r m a n O., D e m m i n g B. Photon yield of O2 evolution and chlorophyll
fluorescence characteristics at 77K among vascular plants of diverse origins // Planta.
1987. Vol. 170. P. 489-504.
6. C a r t e r G. A. Primary and secondary effects of water content on the spectral
reflectance of leaves // Am. J. Bot. 1991. Vol. 78. P. 916–924.
7. C a r t e r G. A. Responses of leaf spectral reflectance to plant stress // Am. J.
Bot. 1993. Vol. 80. P. 239–243.
8. C a r t e r G. A. Ratios of leaf reflectances in narrow wavebands as indicators of
plant stress // Int. J. Remote Sens. 1994. Vol. 15 P. 697–703.
9. K r a u s e G. H., W e i s E. Chlorophyll fluorescence and photosynthesis:
the basics // Annu. Rev. Plant Physiol. Plant Mol. Biol. 1991. Vol.42. P. 313–349.
10. M i k a A., P i à t k o w s k i M. Results of 10 year trial of high density
planting of McIntosh and Mcspur apple trees // Acta Hort. 1986. Vol. 160. P. 293–304.
11. M a n t i n g e r H., V i g l J. Superspindel und Schlanke Spindel im
Vergleich // OBSTB. WEINB. 1999. Vol. 9 P. 259–262.
12. O g r e n E., E v e n s J. R. Photoinhibition ofphotosynthesis in situ in
species of Eucalyptus//Australian Journal of Plant Physiology,1992. Vol. 19 P. 224–232.
13. S h o l e s J. D. and H o r t o n P. Photosynthesis and chlorophyll
fluorescence: simultaneous measurements // Methods in comparative plant ecology.
Chapman and Hall. London, 1993.
369
14. S t a m p a r, F., H u d i n a, M., U s e n i k, V., D o l e n c, K. and
Z a d r a v e c, P. Influence of planting densities on vegetative and generative growth
and fruit quality of apple (Malus Domestica Bork.) // Acta Hort. (ISHS) 1998. Vol. 513.
P. 349–356.
15. S h r e i b e r, U., H o r m a n n, H., N e u b a u e r, C. and
K l u g h a m m e r, C. Assessment of photosystem II photochemical quantum yield by
chlorophyll fluorescence quenching analysis // Aust. J. Plant Physiol. 1995. Vol. 22. P. 209–220.
16. Ð a b a j e v i e n ë G., U s e l i s N., D u c h o v s k i s P. ‘Auksio’
veislës obelø su P 22 poskiepiu fotosintezës pigmentø tyrimai ávairiø konstrukcijø
intensyviuose soduose // Sodininkystë ir darþininkystë 2005. Vol. 24. N 4. P. 57–71.
17. Ð a b a j e v i e n ë G., U s e l i s N., D u c h o v s k i s P. ‘Auksio’
veislës obelø su P 22 poskiepiu fotosintezës pigmentø sistemos formavimasis ávairiø
konstrukcijø intensyviuose soduose // Sodininkystë ir darþininkystë 2005. Vol.24. N 4.
P. 57–71.
18. U s e l i s N. Þemaûgiø obelø augumas ir produktyvumas ávairiø konstrukcijø
deranèiuose soduose // Sodininkystë ir darþininkystë. 2003. Vol. 22. N 1. P. 3–13.
19. W e r t h e i m S. J., D e J a g e r A. J., D u y z e n, U. J. V. P.
Comparison of single-row and multi-row planting systems with apple, with regard to
productivity, fruit size and color and light conditions // Acta Hort. 1986. Vol.160. P. 243–258.
20. W i d m e r A., K r e b s C h. Influence of planting density and tree form on
yield and fruit quality of Golden Delicious and Royal Gala apples // Acta Hort. 2001. Vol.
557. P. 235–241.
SODININKYSTË IR DARÞININKYSTË. MOKSLO DARBAI. 2006. 25(3).
364–370.
‘AUKSIO’ VEISLËS OBELØ SU P 22 IR P 60 POSKIEPIAIS CHLOROFILØ
FLUORESCENCINIØ RODIKLIØ TYRIMAI ÁVAIRIØ KONSTRUKCIJØ
INTENSYVIUOSE SODUOSE
G. Ðabajevienë, J. Sakalauskaitë, V. Ðlapakauskas, N. Uselis, P. Duchovskis
Santrauka
2005 m. Lietuvos sodininkystës ir darþininkystës institute tirti fluorescenciniai rodikliai
‘Auksio’ veislës obelø su P 22 ir P 60 poskiepiais lapuose. Tirti vaismedþiai su laibosios
verpstës, V formos laibosios verpstës, paprastosios verpstës, V formos superverpstës,
superverpstës formø ir laisvai auganèiais lyderiniais vainikais. Vaismedþiai su P 22 poskiepiu
pasodinti 3 x 1,5 m; 3 x 1,25 m; 3 x 1 m ir 3 x 0,75 m tankumu, o vaismedþiai su P 60
poskiepiu – 3 x 1 m; 3 x 0,75 m; 3 x 0,5 m ir 3 x 0,25 m. Gauti rezultatai rodo, kad dël tankumo
kilusi didesnë medþiø konkurencija veikia kaip stresas. Taèiau fluorescenciniø rodikliø
augimas tankiausiai pasodintø obelø lapuose rodo konkurencinës átampos atsiradimà.
Didþiausia kvantinë iðeiga ir elektronø transportas nustatyti V formos superverpstës ir
V formos laibosios verpstës vainikus turinèiø vaismedþiø lapuose. Tai rodo, kad atvira
V forma uþtikrina optimalø ðviesos pasiskirstymo lygá, kuris lemia aukðtà fotocheminá
efektyvumà vaismedþiø lapuose. Fluorescenciniø rodikliø skirtumai obelø su skirtingais
poskiepiais lapuose rodo, kad vaismedþiø reakcija á tarpusavio konkurencijà priklauso ir
nuo poskiepio.
Reikðminiai þodþiai: elektronø transportas, fluorescencija, kvantø iðeiga, obelys,
poskiepiai, sodo konstrukcija, tankumas.
370
ATMINTINË AUTORIAMS, RAÐANTIEMS Á MOKSLO DARBUS
„SODININKYSTË IR DARÞININKYST˓
Straipsnio rankraðèio pateikimo - priëmimo procedûra
Straipsnius redakcijai gali pateikti bet kurie Lietuvos ar uþsienio ðalies mokslo
darbuotojai bei asmenys, dirbantys moksliná darbà. Ne mokslo darbuotojo
straipsnis turi bûti paraðytas kartu su mokslo darbuotoju.
Rankraðtis redakcijai siunèiamas paðtu dviem egzemplioriais, atspausdintas
kompiuteriu popieriuje, prisilaikant toliau tekste nurodytø reikalavimø. Pateiktas
straipsnio rankraðtis uþregistruojamas ir perduodamas redkolegijos nariui,
kuruojanèiam ðià sritá. Jis ávertina, ar rankraðèio turinys ir forma atitinka
svarbiausius periodiniams straipsniams keliamus reikalavimus. Rankraðèiai, kurie
buvo atmesti pirmojo vertinimo metu, su paaiðkinamuoju raðtu gràþinami autoriui.
Jeigu straipsnio tinkamumas nekelia abejoniø, redkolegijos narys skiria du
recenzentus.
Pataisytà rankraðtá autorius per deðimt dienø turi atsiøsti el. paðtu
arba paðtu redakcijai kartu su elektronine laikmena (diskeliu).
Reikalavimai rankraðèiui
Struktûra ir apimtis
Rankraðèio forma turi atitikti periodiniams moksliniams straipsniams keliamus
reikalavimus. Teksto ir jo sudëtiniø daliø seka tokia:
- Straipsnio pavadinimas (ne daugiau kaip 10 þodþiø);
- Autoriaus vardas, pavardë
Vardas raðomas maþosiomis, pavardë - didþiosiomis raidëmis. Jeigu yra keli
autoriai, raðoma maþëjanèia jø autorystës indëlio tvarka.
- Institucija, adresas, elektroninis paðtas;
Pagrindinis tekstas
- Santrauka (iki 1400 raðybos þenklø arba 250 þodþiø);
Labai glaustai pateikiami tikslai, sàlygos, svarbiausieji rezultatai.
- Reikðminiai þodþiai (ne daugiau kaip 10, abëcëlës tvarka);
- Ávadas
Trumpai iðdëstoma nagrinëjama problema, ankstesnieji kitø panaðiø tyrimø
rezultatai, darbo reikalingumas, originalumas. Nurodomas darbo tikslas.
- Tyrimo objektas ir metodai;
- Rezultatai
Trumpai iðdëstomi tyrimø metu surinkti duomenys, dokumentai (lentelës,
grafikai).
- Aptarimas
371
Aptariami, bet nekartojami "Rezultatø" skyrelyje pateikti duomenys,
palyginami su kitø autoriø duomenimis, aiðkinamos tirtø reiðkiniø prieþastys,
keliamos naujos idëjos, hipotezës.
- Iðvados;
- Literatûra
Rekomenduojama talpinti ne maþiau kaip 10 naujausiø raðoma tema literatûros
ðaltiniø.
- Santrauka anglø kalba (600-1400 sp. þenklø);
- Padëka (neprivaloma);
Straipsnio pabaigoje turi bûti autoriaus (-iø) ar kitø uþ straipsná atsakingø
asmenø paraðas bei pasiraðymo data.
Straipsniai, kurie paraðyti remiantis netradiciniais bandymø duomenimis ir jø
rezultatais, gali turëti ir kitokias struktûrines teksto dalis.
Straipsnis turi bûti ne daugiau kaip 10-15 puslapiø apimties, áskaitant
lenteles ir paveikslus (didesnës apimties straipsniai derinami su redkolegijos
pirmininku).
Teksto parengimas
Straipsnis raðomas lietuviø, anglø ar rusø kalba IBM tipo kompiuteriu,
spausdinamas MO Microsoft WORD for Windows 95; 98; 2000 teksto
redaktoriais TIMES NEW ROMAN 12 dydþio ðriftu, vienoje A4 formato
(210 x 297 mm) lapo pusëje, atstumas tarp rankraðèio eiluèiø - 1 (single),
tekstui po recenzijø - 1,5 (1,5 lines), iðlyginamas ið abiejø pusiø, pateikiamas
elektroninëje
laikmenoje
1,44 MB diskelyje. Paraðèiø plotis virðuje - 2 cm, apaèioje - 2 cm, deðinëje 1,5 cm, kairëje - 3 cm.
Paryðkintai (Bold) raðoma straipsnio pavadinimas visomis kalbomis, antraðtës
bei svarbiausieji struktûriniai elementai (santrauka, ávadas, metodai, sàlygos,
rezultatai, diskusija, iðvados, literatûra). Kursyvu (Italic) raðomi lotyniðki
augalø rûðiø, genèiø, ligø, kenkëjø ir mikroorganizmø pavadinimai. Augalø veisliø
pavadinimai raðomi viengubose kabutëse.
Cituojamas ðaltinis tekste nurodomas lenktiniuose skliaustuose (autoriaus
pavardë, metai).
Lentelës
Lenteliø duomenys neturi dubliuotis su paveikslø ar kitos iliustracinës
medþiagos informacija.
Lenteliø tekstas raðomas lietuviø ir anglø kalbomis. Jeigu straipsnis paraðytas
rusø kalba - rusø ir anglø. Jei lietuviø ir anglø tekstai talpinami vienoje eilutëje,
tarp jø dedamas þenklas /. Lentelës teksto dalys vertikaliomis ir horizontaliomis
372
linijomis neatskiriamos. Horizontaliomis linijomis atskiriamos tik lentelës metrikos
dalys bei lentelës pabaiga. Lentelës padëtis puslapyje tik vertikali (Portrait).
Bandymø variantai lentelëse neturi bûti þymimi skaièiais, sudëtingomis
santrumpomis, o pateikiami visa arba suprantamai sutrumpinta apraðo forma.
Statistiniai duomenys, skaièiai ir skaitmenys
Pageidautina detaliai apraðyti taikytus tyrimø metodus ir nurodyti jø originalius
ðaltinius. Labai svarbi informacija apie lauko, vegetaciniø ir kt. bandymø iðdëstymo
schemà ir jos pasirinkimo motyvus. Lentelëse ir paveiksluose pateikiami duomenys
privalo bûti statistiðkai apdoroti: apskaièiuoti vidurkiai, jø kitimo paklaidos,
ryðio ir jo tikslumo koeficientai, patikimo skirtumo ribos (priimtiniausia apskaièiuoti
95% arba ir - 90,99% tikimybës lygiu) ir pan. Rodikliø þymëjimo santrumpos
turi bûti paaiðkintos, jeigu jos neatitinka tarptautiniø ISO standartø [13].
Reikðminiø skaièiø turi bûti ne daugiau negu leidþia bandymo metodas. Variantø
vidurkiai turi bûti suapvalinti iki 1/10, apskaièiuotos jø standartinës paklaidos.
Kieká þymintys skaièiai raðomi arabiðkais skaitmenimis, pvz.: 15 tonø, o eilæ
þymintys gali bûti raðomi ir romëniðkai, ir arabiðkai, pvz.: XX amþius, 2 pavyzdys.
Skaièiai nuo vieneto iki devyniø raðomi þodþiu, iðskyrus, kai jie reiðkia
matavimo vienetø dydá (pvz.: 5 km, bet "trys variantai") arba yra prasminë skaièiø
seka (pvz.: 6, 9, 12 tarpsnis). Tarp daugiaþenkliø skaièiø klasiø paliekamas tarpelis,
pvz., 42 351. Procentai þymimi %, kai reiðkia konkretø skaièiø, taèiau "procentiniai
vienetai" raðomi tik þodþiu. Deðimtainës trupmenos dalys nuo sveikøjø skaièiø
atskiriamos kableliu.
Paveikslai
Visa iliustracinë medþiaga - brëþiniai, grafikai, diagramos, fotografijos, pieðiniai
ir kt. - vadinami bendru paveikslø vardu. Tekstas juose raðomas lietuviø ir anglø
kalbomis.
Paveikslai turi bûti nespalvoti, padaryti Microsoft Office 95, 98, 2000
paketo elektroninëje lentelëje EXCEL arba naudojantis kitomis ðio paketo
programomis ir pateikiami straipsnio tekste bei atskira EXCEL byla
diskelyje. Ranka pieðti, braiþyti, kopijuoti paveikslai nepriimami arba jie
perdaromi pagal galiojanèius maketavimo ákainius. Redakcija pasilieka teisæ keisti
jø formatà pagal straipsnio ar viso leidinio dizainà.
Áraðai ir simboliai paveiksluose turi bûti paraðyti ne maþesniu kaip 10 ðrifto
dydþiu. Paveikslø blokø dalys turi bûti suþymëtos raidëmis
a, b, c ir t.t.
Literatûros sàraðas
Á literatûros sàraðà gali bûti átraukiama:
- straipsniai, atspausdinti moksliniuose periodiniuose þurnaluose,
373
moksliniuose recenzuotuose leidiniuose ( knygose, monografijose), moksliniø
konferencijø, simpoziumø, kuriø medþiaga buvo recenzuota arba struktûros ir
apimties poþiûriu atitinka moksliniø periodiniø leidiniø straipsniø reikalavimus,
straipsniø rinkiniuose;
- mokslinës knygos, monografijos, maþesnës apimties recenzuoti ir
tik iðimtinai mokslinës paskirties leidiniai (t.y. disertacijø mokslo laipsniui
ágyti santraukos) arba jø dalys;
Sàraðe rekomenduojama talpinti ne maþiau kaip deðimt literatûros ðaltiniø.
Visi jie turi bûti cituojami tekste. Du treèdaliai ðaltiniø turëtø bûti ne senesni kaip
ketveriø-ðeðeriø metø, o senesni - tik ypatingai reikðmingi ir svarbûs. Autoriaus
cituotini tik tie darbai, kurie tiesiogiai siejasi su nagrinëjama tema.
Mokslinës ataskaitos, rankraðtinë medþiaga, vadovëliai, þinynai, konferencijø
medþiaga (tezës ar trumpi paraneðimai), rekomendacijos, reklaminiai bukletai
bei laikraðèiai literatûros ðaltiniais nelaikomi ir á sàraðà neátraukiami. Nuorodos á
standartus, þinynus ir kitus normatyvinius teisinius dokumentus nurodomos puslapiø
iðnaðose.
Uþsienyje leistø þurnalø, konferencijø rinkiniø ir kt. pavadinimai netrumpinami.
Literatûra sàraðe suraðoma abëcëlës tvarka.
Knygos
Bulavas J. Augalø selekcija. V.: Mintis, 1963. P. 2-15.
Straipsniai ið moksliniø þurnalø ir periodiniø leidiniø
Juozaitis J. Pomidorø auginimas // Sodininkystë ir darþininkystë. Babtai,
2000. T. 20. P. 4-9.
Koch J. Plough depth // Soil Science. 1998. Vol. 15. N 2. P. 12-15.
Disertacijø santraukos
Simonaitis J. Þirniø agrotechnika: daktaro disertacijos santrauka. Kaunas,
1988. 25 p.
374
GUIDELINES FOR THE PREPARATION AND SUBMISSION OF ARTICLES
TO THE VOLUMES OF SCIENTIFIC WORKS „SODININKYSTË IR
DARÞININKYST˓
Rules for Submission – Acceptance of Papers.
Papers can be contributed by Lithuanian and foreign researchers or persons
carrying out scientific research. The latter’s paper will be accepted only when the
coauthor is an investigator.
Manuscripts should be sent by mail printed out in two copies taking in account
following instructions. The manuscript will be registered and submitted to the member
of the Editorial Board in charge. He(she) will evaluate if the contents and the form
confirm with the main requirements for periodical articles. Manuscripts rejected
during the first evaluation will be returned to the author with explanatory remarks. If
the article is approved the member of the Editorial Board appoints two reviewers.
The author must return the corrected manuscript to the Editorial Board
in ten days by email or by mail in a diskette.
Standard Manuscript
Structure and length
The form of a manuscript has to confirm with requirements for periodical
scientific articles. The paper should be organized in the following order:
-Title (should not exceed 10 words);
-Author(s)’ names
The name should be written in small letters, the surname – in capital letters. If
there is more than one author they are listed according to their input to the paper.
-Institution(s), address, email address;
-Research report:
-Abstract (should not exceed 1400 characters or 250 words);
Should contain the statement of the aims, methods and main results in short.
-Key words (should not exceed 10 words in alphabetical order);
-Introduction
Should present the investigated subject, results of earlier related research, reasons
of the study, innovation.
-Materials and methods;
-Results
Should present concisely the collected data during investigation, documentation
(tables, figures).
-Discussion
Should not repeat results presented in “Results” but should interpret them
with reference to the results obtained by other authors, explain the reasons of the
investigated phenomena, raise new ideas, hypotheses.
-Conclusions;
-References
Should be kept to a minimum of 10 latest references on this theme.
-Summary in English (up to 2000 characters or 350 words);
-Acknowledgements (not compulsory);
375
The paper should be ended by a signature of the author(s) or other persons
responsible for the article and the date.
Articles written based on non-traditional trial data and the obtained results may
have other than traditional structural parts of a paper.
The article should not exceed 10-15 pages, tables and figures included (longer
articles are agreed with the chairman of the Editorial Board).
Text preparation
The manuscripts should be submitted in Lithuanian, English or Russian, typed
by IBM type computer, used MO Microsoft WORD for Windows 95; 98; 2000
word-processor format, the font to be typed - TIMES NEW ROMAN size 12, on
A4 paper (210 x 297 mm) one side, for a manuscript – single spaced, for the text
after reviews - 1,5 lines, justified, in a 1,44 MB diskette. Margins: top - 2 cm,
bottom - 2 cm, right -1.5 cm, left - 3 cm.
In bold are written the title of the paper in all languages, headings and all main
structural elements (abstract, introduction, materials, methods, results,
discussion, conclusions, references). In Italic are written Latin names of species,
genera, diseases, pests and microorganisms. Cultivar is it be placed within single
quatation marks.
Tables
If results are already given in figures, tables should not be used. Double
documentation is not acceptable.
Text in tables is written in Lithuanian and English languages. If the text is written
in Russian – in Russian and English. If Lithuanian and English texts are in one line
they are separated by /. Do not use vertical and horizontal lines to separate parts of
the text. A horizontal line separates only headings of columns and the end of the
table. Orientation in a page only vertical (Portrait).
Trial variants in tables should not be numbered or submitted in complicated
abbreviations. Tables should be self explanatory, and if there are abbreviations, they
should be understandable.
Statistical data, figures, numerals
It is desirable to describe in detail the applied research methods and indicate
references. The information on the scheme (design) of field, vegetative and other
trials and motivation of their choice are very important. Data presented in tables and
figures must be statistically processed: means, standard errors, correlation
coefficients, significance of differences, (most acceptable at 95% or and – 90.99%
level), etc. calculated. Abbreviations of parameters should be explained if they are
not international standard abbreviations (ISO) [13].
Value figures should not be more than the trial method allows. Means of values
should be rounded off to 1/10, their standard errors calculated.
For figures indicating quantity should be used Arabic numerals, e.g.: 15 tons,
and for consecutive numbering can be used both Roman and Arabic numerals, e.g.:
XX century, 2nd sample.
Numbers from one to nine are written in words, except when they mean
measurement size (e.g.: 5 km, but “three variants”) or numbered consecutively (e.g.:
phase 6, 9, 12). In many-figured numbers between classes an interval is made, e.g.,
376
42 351. Percent is noted as %, when a specific number is implied, though „percent
unit“ is written in words. In decimals use the decimal point.
Figures
All illustrations - drawings, graphs, diagrams, photographs are considered as
figures. The text in them is written in Lithuanian and English.
Figures must be drafted in black color in Microsoft Office 95, 98, 2000 packet
EXCEL or other programs of this packet and included into the text and submitted
as a separate EXCEL file in a diskette. Drawings must be professionally drafted
or they can be redrafted by a professional and the work will be paid by the author
according to the price list. Notice that the Editorial Board has the right to change
their format according to the design of the article or the whole publication.
Letters and symbols in figures are recommended not smaller than size 10. Block
parts of figures should be numbered consecutively by letters a, b, c, etc.
References
Into references can be included:
-articles, published in scientific periodical journals, scientific reviewed
publications (books, monographs), article collections of scientific conferences and
symposiums whose papers were reviewed or they meet the requirements of scientific
periodical publications with reference to the structure and the length of the article;
-scientific books, monographs, reviewed publications of smaller volume
and exclusively for scientific purpose (i.e. abstracts of theses to obtain a
scientific degree) or their parts;
It is recommended to include a minimum of 10 references. All of them must be
cited in the text. Two thirds of references should be not older than four-six years,
and if older – only very significant. Cited are only these works, which are directly
related to the investigated theme.
Scientific reports, manuscripts, textbooks, reference books, conference
proceedings (theses or short presentations), recommendations, pamphlets, articles
in newspapers are not considered as references and are not included into references
list. References to standards, reference books or other regulations and rules are
indicated in footnotes.
Names of journals, volumes of conference articles, etc, are not abbreviated.
The reference list should be arranged in alphabetical order.
Book:
Wertheim S.J. Rootstock guide. Wilhelminadorp. 1998. 144 p.
Journal article
Johnson D.S. Controlled atmosphere storage of apples in UK // Acta horticulturae.
1999. Vol. 485. P.187-193.
Koch J. Plough depth // Soil Science. 1998. Vol. 15. N 2. P. 12-15.
Thesis abstract
Karkleliene R. Inheritance of quantitative characters and estimation of combining
ability in carrots: summary of doctoral dissertation. Babtai, 2001.
43 p.
377
TURINYS
D. K v i k l y s. Obelø ir kriauðiø poskiepiø tyrimai Lietuvoje ......................... 3
F. M a a s. Kriauðiø ir svarainiø poskiepiø tinkamumas intensyviems
kriauðiø sodams ........................................................................................... 13
S. E r c i s l i, A. E s i t k e n, E. O r h a n, O. O z d e m i r. Vidutinio
klimato sàlygomis auganèiø vaismedþiø poskiepiai Turkijoje: apþvalga ..... 27
V. S a m u s, S . G a d z h i e v, V. P o p l a v s k i y, N. D r a b u d k o.
Vaismedþiø poskiepiai Baltarusijoje .............................................................. 34
J. L e w k o, A. S a d o w s k i, K. Ú c i b i s z. Kriauðiø sodinukø
augimo ir kokybës priklausomumas nuo poskiepiø ir augimo sezono ....... 39
M. S i t a r e k, T. J a k u b o w s k i. Dviejø abrikosø veisliø, áskiepytø
á skirtingus sëklinius poskiepius, prigijimas ir sodinukø augimo
rodikliai......................................................................................................... 47
D. G e l v o n a u s k i e n ë, B. G e l v o n a u s k i s, A . S a s n a u s k a s.
Poskiepiø átaka koloniniø obelø sodinukø augimui medelyne ..................... 51
M. L i c z n a r - M a ù a ñ c z u k, I. S o s n a. Poskiepio átaka skirtingø
veisliø abrikosø sodinukø kokybei .............................................................. 57
T. K r a s i n s k a y a, N. K u k h a r c h y k. Jonø mainø terpës
(Biona-112 ir Biona-312) átaka Prunus L. poskiepiø biocheminiams
rodikliams adaptacijos ex vitro metu. ......................................................... 62
E. O r h a n, S. E r c i s l i, A. E s i t k e n, F. S a h i n. ‘Texas’ ir
‘Nonpareil’ veisliø migdolø sëjinukø ðalutiniø ðaknø augimo skatinimas
bakterijomis, ðakneliø trumpinimu ir ISR .................................................... 71
E. D z i e d z i c, M. M a ù o d o b r y. Vegetatyviniai vyðniø poskiepiai
audiniø kultûroje .......................................................................................... 77
S. T a b a k o v, A. Yo r d a n o v. Kai kuriø medelyne vegetatyviniu
bûdu dauginamø obelø poskiepiø apibûdinimas .......................................... 85
E. G u d a r o w s k a, A. S z e w c z u k. Obelø veisliø ‘Fiesta’ ir ‘Pinova’
derliaus priklausomumas nuo sodinukø amþiaus ir dauginimo bûdø ......... 90
E. G u d a r o w s k a, A. S z e w c z u k, D. D e r e ñ. Obelø genëjimo
aukðèio medelyne átaka jø kokybei ir derliui ................................................ 98
J. K o p y t o w s k i, B. M a r k u s z e w s k i, J. G u r s z t y n. Kai
kuriø technologiniø priemoniø átaka obelø kokybës rodikliams .................. 104
T. L. R o b i n s o n, S. A. H o y i n g, R. L. A n d e r s e n. Þemaûgiø
treðniø poskiepiø produktyvumas Jungtiniø Amerikos Valstijø Ðiaurës
Rytuose ........................................................................................................ 113
N. U s e l i s. Obelø su P 60 poskiepiu sodinimo sistemø ir vainiko formø
átaka vaismedþiø produktyvumui ir vaisiø kokybei ..................................... 124
N. U s e l i s, G. Ð a b a j e v i e n ë, P. D u c h o v s k i s. Sodinimo
schemø ir vainiko formø átaka vaismedþiø su P 22 poskiepiu
produktyvumui ir vaisiø kokybei ................................................................. 133
D. W r o n a, A. S a d o w s k i. ‘Elise’ obelø veislës su 18 poskiepiø
palyginimas V formos sodinimo sistemoje ................................................. 144
378
N. U s e l i s. Poskiepiø ir sodinimo schemø átaka ‘Ligol’ veislës obelø
produktyvumui ir vaisiø kokybei ................................................................. 151
P. B i e l i c k i, A. C z y n c z y k, B. B a r t o s i e w i c z. Preliminarus
‘Celeste’ veislës obelø su þemaûgiais poskiepiais ávertinimas Centrinëje
Lenkijoje ....................................................................................................... 158
J. Ve r c a m m e n, G. Va n D a e l e, A. G o m a n d. ‘Jonagold’
veislei tinkamø þemaûgiø poskiepiø tyrimas ............................................... 164
A. C z y n c z y k, P. B i e l i c k i, B. B a r t o s i e w i c z. ‘Jonagold’ ir
‘Ligol’ veisliø obelø augimas ir derëjimas su M.9, P 22 subklonais ir kai
kuriais lenkiðkais poskiepiais ....................................................................... 173
T. L. R o b i n s o n, G. F a z i o, H. S. A l d w i n c k l e,
S. A. H o y i n g, N. R u s s o . Geneva® obelø poskiepiø
savybiø vertinimas Rytinës JAV dalies soduose .......................................... 181
N. U n i v e r, T. U n i v e r, K. T i i r m a a. Penkiø poskiepiø átaka
keturiø veisliø obelø augimui ir derliui jauname sode .................................. 192
E. R u b a u s k i s, M. S k r i v e l e. ‘Auksio’ veislës obelø su skirtingais
poskiepiais augimas ir derëjimas Latvijoje ................................................... 199
V. O s t a p e n k o. Poskiepio átaka ‘Florina’ veislës obelø derlingumui
ir vaisiø kokybei Pietø Rusijos sàlygomis ................................................... 207
A. P a p a c h a t z i s. Poskiepio átaka ‘Stella’ veislës vyðniø augimui ir
reprodukcinëms savybëms derëjimo laikotarpiu ......................................... 212
J. Ve r c a m m e n, G. Va n D a e l e, T. Va n r y k e l. Gisela 5
poskiepio naudojimas treðnëms ................................................................... 218
Z. T o m a s z e w s k a, B. N y c h n e r e w i c z. Poskiepiø átaka
treðniø augimui ir derëjimui ......................................................................... 224
L. R i a z a n o v a, V. O s t a p e n k o. Slyvø veisliø ir poskiepiø deriniø
ávertinimas Pietø Rusijos sàlygomis ............................................................ 230
E. D z i e d z i c, M. M a ù o d o b r y, W. L e c h. Intarpø átaka slyvø
veislës ‘Èaèanska najbolia‘ vaismedþiø augimui, derliui ir vaisiø
kokybei......................................................................................................... 235
J. L a n a u s k a s. Poskiepiø átaka ‘Stanley’ ir ‘Kauno vengrinës’ veisliø
slyvø vaismedþiø augimui ir derëjimui ....................................................... 243
I. S o s n a. Keliø veisliø slyvø su keturiais poskiepiais ávertinimas .............. 250
N. K v i k l i e n ë, D. K v i k l y s. Poskiepio átaka ‘Auksio’ vaisiø
kokybei ir nokimui ....................................................................................... 258
M. G à s t o ù, J. S k r z y ñ s k i. Skirtingø augimà stabdanèiø
metodø átaka mikroelementø kiekiui obelyse ............................................... 264
J. S a k a l a u s k a i t ë, G. S t a n i e n ë, V. S t a n y s,
P. D u c h o v s k i s, G. S a m u o l i e n ë,
K. B a r a n a u s k i s, A. U r b o n a v i è i û t ë, V. R e v i n,
A. L u k a t k i n. Obelø poskiepiø M.9 ir B.396 atsparumas kadmio
jonø poveikiui in vitro .................................................................................. 273
J. S a k a l a u s k a i t ë, D. K v i k l y s, J. L a n a u s k a s,
P. D u c h o v s k i s. Sausros sukelto streso átaka obelø poskiepiø
biomasei, sausos masës pasiskirstymui ir lapø plotui ................................. 283
379
Z. S. G r z y b, M. S i t a r e k. Skirtingø poskiepiø átaka
‘Dàbrowice prune’ veislës slyvø augimui, derliui ir vaisiø kokybei
nualintoje dirvoje .......................................................................................... 292
V. L i c h e v, A. P a p a c h a t z i s. Deðimties poskiepiø átaka ‘Bigarreau
burlat’ veislës vyðniø þiedø atsparumui ðalèiams ........................................ 296
Yu - L i a n g C a i, G u i - F a n g Z h a o, D o n g - W e i C a o. Laukiniø
vyðniø genetinës variacijos tyrimai panaudojant RAPD analizæ .................. 302
A. L i s e k, M. K o r b i n, E. R o z p a r a. Paprastas treðniø PHL
poskiepiø identifikavimas panaudojant RAPD þymenis .............................. 316
E. H a a k, D. K v i k l y s, J. L e p s i s. Cydonia ir Pyrus
poskiepiø palyginimas Estijoje, Latvijoje ir Lietuvoje .................................. 322
G. L. R e i g h a r d, T. B e c k m a n, R. B e l d i n g, B. B l a c k,
J. C l i n e, W. C o w g i l l, R. G o d i n, M. K a p s,
T. L i n d s t r o m, D. Q u e l l e t e, L. S t e i n, K. T a y l o r,
C. W a l s h, M. W h i t i n g, T. R o b i n s o n. Prunus poskiepiø
vertinimas 2001 m. NC-140 persikø bandyme ........................................... 327
D. K v i k l y s, N. K v i k l i e n ë, A. B i t e, J. L e p s i s,
T. L u k u t, E. H a a k. Baltijos poskiepiø tyrimai: 12 poskiepiø
ávertinimas atliekant tyrimus su ‘Auksio’ veislës obelimis ......................... 334
M. A b o l i n s. Obelø veisliø ir poskiepiø deriniø augimo ritmø sutapimo
ávertinimas .................................................................................................... 342
B. G e l v o n a u s k i s, A. B r a z a i t y t ë, A. S a s n a u s k a s,
P. D u c h o v s k i s, D. G e l v o n a u s k i e n ë. Morfologinës ir
fiziologinës koloniniø obelø veisliø savybës ................................................ 350
G. Ð a b a j e v i e n ë, D. K v i k l y s, P. D u c h o v s k i s. Poskiepiø átaka
‘Auksio’ veislës obelø fotosintetiniø pigmentø sistemai ............................. 357
G. Ð a b a j e v i e n ë, J. S a k a l a u s k a i t ë, V. Ð l a p a k a u s k a s,
N. U s e l i s, P. D u c h o v s k i s. ‘Auksio’ veislës obelø su
P 22 ir P 60 poskiepiais chlorofilø fluorescenciniø rodikliø tyrimai
ávairiø konstrukcijø intensyviuose soduose ................................................. 364
Atmintinë autoriams, raðantiems á mokslo darbus „SODININKYSTË IR
DARÞININKYST˓ .................................................................................... 371
380
CONTENTS
D. K v i k l y s. Apple and pear rootstock research in Lithuania .................... 3
F. M a a s. Evaluation of pyrus and quince rootstocks for high density
pear orchards ............................................................................................... 13
S. E r c i s l i, A. E s i t k e n, E. O r h a n, O. O z d e m i r. Rootstocks
used for temperature fruit trees in Turkey: an overview ........................... 27
V. S a m u s, S . G a d z h i e v, V. P o p l a v s k i y, N. D r a b u d k o.
Rootstocks of Fruit crops in Belarus .......................................................... 34
J. L e w k o, A. S a d o w s k i, K. Ú c i b i s z. Growth and quality of
pear maiden trees depending on rootstok and growing season ................. 39
M. S i t a r e k, T. J a k u b o w s k i. Bud–take and maiden tree
parameters of two apricot cultivars budden on different seedling
rootstocks .................................................................................................... 47
D. G e l v o n a u s k i e n ë, B. G e l v o n a u s k i s, A . S a s n a u s k a s.
Impact of rootstocks on columnarapple tree growth in a nursery ............ 51
M. L i c z n a r - M a ù a ñ c z u k, I. S o s n a. Quality of maiden
apricot trees depending on rootstock and cultivar ..................................... 57
T. K r a s i n s k a y a, N. K u k h a r c h y k. The influence of ion
exchange substrates (Biona-112 and Biona-312) on biochemical
parameters of Prunus L. rootstocks during adaptation ex vitro................. 62
E. O r h a n, S. E r c i s l i, A. E s i t k e n, F. S a h i n. Lateral root
induction by bacteria, radicle cut off and IBA treatments of almond
cv. ‘Texas’ and ‘Nonpareil’ seedlings ......................................................... 71
E. D z i e d z i c, M. M a ù o d o b r y. Vegetative cherry rootstocks
in tissue culture ............................................................................................ 77
S. T a b a k o v, A. Yo r d a n o v. Performance of some vegetatively
propagated apple rootstocks in the nursery ................................................ 85
E. G u d a r o w s k a, A. S z e w c z u k. Yielding of apple tree
cvs. ‘Fiesta’ and ‘Pinova’ depending on the age of planting material
and methods of its production in a nursery ................................................
of the height of pruning of apple trees in a nursery on their quality .......... 98
J. K o p y t o w s k i, B. M a r k u s z e w s k i, J. G u r s z t y n. The
effect of selected agricultural practices on quality features of apple
trees ............................................................................................................. 104
T. L. R o b i n s o n, S. A. H o y i n g, R. L. A n d e r s e n.
Performance of dwarfing cherry rootstocks in the Northeastern
United States ................................................................................................ 113
N. U s e l i s. Influence of planting schemes and crown forms of apple
tree on rootstock P 60 on productivity and fruit quality ............................ 124
N. U s e l i s, G. Ð a b a j e v i e n ë, P. D u c h o v s k i s. Influence of
planting schemes and crown forms on productivyti and fruit quality
of apple trees on rootstock P 22 ................................................................. 133
D. W r o n a, A. S a d o w s k i. Comparison of 18 rootstocks for
apple tree cv. ‘Elise’ in V planting system .................................................. 144
381
N. U s e l i s. Influence of rootstocks and planting schemes of apple
tree cv. ‘Ligol’ on productivity and fruit quality ........................................ 151
P. B i e l i c k i, A. C z y n c z y k, B. B a r t o s i e w i c z. Preliminary
evaluation of apple tree cultivar ‘Celeste’ on dwarf rootstocks
in central Poland .......................................................................................... 158
J. Ve r c a m m e n, G. Va n D a e l e, A. G o m a n d. Search for
a more dwarfing rootstock for ‘Jonagold’ ................................................. 164
A. C z y n c z y k, P. B i e l i c k i, B. B a r t o s i e w i c z. Growth and
yielding of ‘Jonagold’ and ‘Ligol’ apple trees on M.9 and P 22
subclones, and some other polish rootstocks............................................. 173
T. L. R o b i n s o n, G. F a z i o, H. S. A l d w i n c k l e,
S. A. H o y i n g, N. R u s s o . Field performance of Geneva®
apple rootstocks in the eastern USA ........................................................... 181
N. U n i v e r, T. U n i v e r, K. T i i r m a a. Effect of five rootstocks
on growth and yield of four apple cultivars in young orchard .................. 192
E. R u b a u s k i s, M. S k r i v e l e. The Yield and growth of apple tree
cultivar ‘Auksis’ on different rootstocks in Latvia ..................................... 199
V. O s t a p e n k o. The influence of rootstock on productivity and
fruit quality of apple-tree cultivar ‘Florina’ under conditions of south
Russia ........................................................................................................... 207
A. P a p a c h a t z i s. Influence of rootstock on growth and reproductive
characteristics of cherry cultivar ‘Stella’ during the period of complete
fruiting ......................................................................................................... 212
J. Ve r c a m m e n, G. Va n D a e l e, T. Va n r y k e l. Use of
Gisela 5 for sweet cherries ......................................................................... 218
Z. T o m a s z e w s k a, B. N y c h n e r e w i c z. The effect of
rootstock on growth and fruitage of sweet cherry .................................... 224
L. R i a z a n o v a, V. O s t a p e n k o. The evaluation of plum tree
cultivar-rootstock combinations under conditions of south Russia .......... 230
E. D z i e d z i c, M. M a ù o d o b r y, W. L e c h. Growth, yielding
and fruit quality of plum cultivar ‘Èaèanska najbolia‘ depending on
the used interstocks ..................................................................................... 235
J. L a n a u s k a s. Effect of rootstock on growth and yield of plum
tree cvs. ‘Stanley’ and ‘Kauno vengrinë’ ................................................ 243
I. S o s n a. Estimation of several plum cultivars on four rootstocks .......... 250
N. K v i k l i e n ë, D. K v i k l y s. Rootstock effect on maturity and
quality of ‘Auksis’ apples ........................................................................... 258
M. G à s t o ù, J. S k r z y ñ s k i. Influence of different dwarfing
methods on Content of microelements in apple tree organs ...................... 264
J. S a k a l a u s k a i t ë, G. S t a n i e n ë, V. S t a n y s,
P. D u c h o v s k i s, G. S a m u o l i e n ë,
K. B a r a n a u s k i s, A. U r b o n a v i è i û t ë, V. R e v i n,
A. L u k a t k i n. Cadmium resistance of apple rootstocks M.9
and B.396 in vitro ........................................................................................ 273
382
J. S a k a l a u s k a i t ë, D. K v i k l y s, J. L a n a u s k a s,
P. D u c h o v s k i s. Biomass production, dry weight partitioning
and leaf area of apple rootstocks under drought strees ............................. 283
Z. S. G r z y b, M. S i t a r e k. The influence of different rootstocks
on the growth, yield and fruit quality of plum tree cv. ‘Dàbrowice
prune’ planted in exhausted poil .................................................................. 292
V. L i c h e v, A. P a p a c h a t z i s. Influence of ten rootstocks on cold
hardiness of flowers of cherry cultivar ‘Bigarreau burlat’ ........................ 296
Yu - L i a n g C a i, G u i - F a n g Z h a o, D o n g - W e i C a o. Studies
on genetic variation in wild cherry using RAPD analysis .......................... 302
A. L i s e k, M. K o r b i n, E. R o z p a r a. Simple identification
of sweet cherry rootstocks PHL using RAPD markers ............................ 316
E. H a a k, D. K v i k l y s, J. L e p s i s. Comparison of
Cydonia and Pyrus rootstocks in Estonia, Latvia and Lithuania ................ 322
G. L. R e i g h a r d, T. B e c h m a n, R. B e l d i n g, B. B l a c k,
J. C l i n e, W. C o w g i l l, R. G o d i n, M. K a p s,
T. L i n d s t r o m, D. Q u e l l e t e, L. S t e i n, K. T a y l o r,
C. W a l s h, M. W h i t i n g, T. R o b i n s o n. Performance of
Prunus rootstocks in the 2001 NC-140 peach trial .................................... 327
D. K v i k l y s, N. K v i k l i e n ë, A. B i t e, J. L e p s i s,
T. L u k u t, E. H a a k. Baltic fruit rootstock studies: evaluation of
12 rootstocks for apple cultivar ‘Auksis’ ................................................... 334
M. A b o l i n s. Evaluation of aoole rootstock-cultivar combinations
by growth rhythms coincidence ................................................................. 342
B. G e l v o n a u s k i s, A. B r a z a i t y t ë, A. S a s n a u s k a s,
P. D u c h o v s k i s, D. G e l v o n a u s k i e n ë. Morphological and
physiological characteristics of columnar apple trees ................................ 350
G. Ð a b a j e v i e n ë, D. K v i k l y s, P. D u c h o v s k i s. Rootstock
effect on photosynthetic pigment system formation in leaves of apple
cv. ‘Auksis’ .................................................................................................. 357
G. Ð a b a j e v i e n ë, J. S a k a l a u s k a i t ë, V. Ð l a p a k a u s k a s,
N. U s e l i s, P. D u c h o v s k i s. Chlorohyll fuorescence
characteristics of cultivar ‘Auksis’ on rootstocks P 22 and P 60 in
high density orchards of different construction ......................................... 364
Guidelines for the preparation and submissiion of articles to the
volumes of scientific works „SODININKYSTË IR DARÞININKYST˓ .....
.................................................................................................................... 375
383
ISSN 0236-4212
Mokslinis leidinys
Lietuvos sodininkystës ir darþininkystës instituto ir
Lietuvos þemës ûkio universiteto mokslo darbai
SODININKYSTË IR DARÞININKYSTË. T.25(3). 1-384.
Redaktorës ir korektorës: Jolanta KRIÛNIENË, Danguolë VANAGAITË
Kompiuteriu maketavo Rima BERÛKÐTIENË
SL 1070. 2006 08 25 24 sp. l Tiraþas 200 egz.
Iðleido Lietuvos sodininkystës ir darþininkystës institutas,
LT-54333 Babtai, Kauno r.
Spausdino UAB „Judex” leidykla-spaustuvë, Europos pr. 122,
LT-46351 Kaunas
Uþsakymo Nr.