soil fertility, fertilization and growth of canadian forests1
Transcription
soil fertility, fertilization and growth of canadian forests1
SOIL FERTILITY, FERTILIZATION AND GROWTH OF CANADIAN FORESTS1 N.W. FOSTER AND I.K. MORRISON GREAT LAKES FOREST RESEARCH CENTRE CANADIAN FORESTRY SERVICE DEPARTMENT OF THE ENVIRONMENT 1983 INFORMATION REPORT O-X-353 ^Presented at the 1979 Annual Meeting of the Canadian Society of Soil Science, Fredericton, New Brunswick ©Minister of Supply and Services Canada 1983 Catalogue No. Fo46-14/353E ISBN 0-662-12691-2 ISSN 0822-210X Copies of this Great Lakes report Forest Canadian Department Sault may be obtained Research Forestry Centre Service of the Environment P.O. Box Ste. Marie, P6A 490 5M7 Ontario from: ABSTRACT Fertilizer test plots nutrient-supplying ability in in adult forest across hypothesis that especially on drier e.g., lack of Canada N sites. with K. to 80 m3 ha"1 The addition an of additional urea 15.6 (Pseudotsuga nsnziesii [Mirb.] pine (Pinus banksiana relationships adjacent limits increase spruce (p. glauca of to P and K are assessing soil from States some experiments support coniferous the species, reported only occasionally; on outwash sands abandoned from agriculture, realized when P and/or K are added (224 kg N ha"1) m3 ha~1 of wocd to natural stands over 4 Franco) and 8.5 m3 ha"1 In Douglas-fir index and being on poorer fir (Abies United growth for Results is not significantly greater than with N alone. Lamb.). between site best evidence demand. of extra wood owr 5 to 10 years after fertilization but generally response average, growth the Responses Ait.), the tree With many species additional growth is with N, balsam to and generally red pine (Pinus resinosa produced 25 have provided relation response sites. balsamea [L.] Mill.), [Moench] Voss), and black with 5-year pine on Douglas-fir forest, responses spruce (Picea spruce (p. produced, over 5 years with jack jack to N have been found, Average red and years were rubens wariana inverse the greatest less Sarg.), [Mill.] with white B.S.P.) (7.1, 4.6, 4.5, and 2.2 m3 ha"1, respectively). The forests use respond of foliar diagnosis and soil chemical analyses to fertilization is discussed. to determine which RESUME La fertilisation en parcelles experimentales a fourni la mailleure base pour evaluer I1 aptitude du sol a repondre aux besoins des arbres en elements nutritifs. Les resultats d'experiences dans des forets adultes du Canada et de regions contigues des E.-U. appuient l'hypothese que la carence en N limite generalement la croissance de certains coniferes, splcialement dans les stations seches. Ce n'est que parfois que example, du pin les reactions rouge (Pinus resinosa Ait.), a P et a K sont signalees; sur les sables par incultes d'epandage fluvio-glaciaire, qui produit 25 a 80 m3/ha de plus de bois, en 5 a 10 ans, apres la fertilisation avec K. les deux sont Eeaucoup d'essences croissent davantage quand P, ajoutes a N, mis generalement la reaction K ou n'est pas significativement plus grande qu'avec N seul. L'apport d'uree (224 kg/ha de N) a des peuplements naturels donne en moyenne 15,6 m3/ha de plus taxifolie. (Pseudotsuga menziesii de bois, en 4 ans, chez le Douglas [Mirb.] Franco) et 8,5 m3/ha, en 5 ans, chez le pin gris (Pinus banksiana Lamb.). Dans les forets de Douglas taxifolie et de pin gris, on a obserwl des relations in\ersement proportionnelles entre l'indice de station et dans les la inferieures rouge (Picea l'epinette reaction a N, stations chez la plus pauvres. le rubens sapin Sarg.), noire (p. mriana En grande augmentation 5 ans, les baumier (Abies l'epinette balsamea blanche (p. [Hill.] B.S.P.) diagnostic foliaire de croissance augmentations [7,1, [L.] glauca 4,6, survenant moyennes Hill.), [l-toench] 4,5 et ont ete l'epinette voss) 2,2 et m3/ha, respectivement]. L'etude traite du et des analyses chimiques comrre moyens de determiner quelles forets reagissent a la fertilisation. du sol TABLE OF CONTENTS Page INTRODUCTION 1 FERTILIZER TRIALS 2 Age 2 Nitrogen Response 3 Nitrogen Source 4 Length of Response 5 Phosphorus and Potassium Response 5 Species-Site Interaction 6 IDENTIFICATION OF MINERAL DEFICIENCIES 10 Foliar Analysis 10 Soil Nutrients 12 WHERE ARE WE IN SOIL FERTILITY? 14 LITERATURE CITED 15 INTRODUCTION The unmanaged forests Soil soil fertility in each relation element growth, and (Anon. 1976). as other raphy , of Soil the for as the well (moisture, climate, nature of plant physiog characteris tics, and a to plants fertility, depth), of quantity properties species determine to status availability soil growth, the necessary its temperature, is of productivity of Acadian forest ity and to 35 in the with soils are than agriculture. The order is Podzolic, Luvisolic, support or Boreal sites. (Rennie soil dominant and soil Organic areas 1972). conditions Canada, of associated the has of been forest and to surpasses age, a in site and reported for sites in the growth black the better basal growth Evert quality to given volume increase 5 region that of For the 1 Acadian quality. As Lcwry spruce produced area increases an (1970) that two better- to four times more growth than poorer sites. although Brunisolic, Gleysolic considerable growth the equals generally those extremes Coastal In example, fertility and from which growth rates in m^ ha""1 yr~' of from 1 with Forest semiraature Boreal fertilization exhibit stage forest regions, forest derived, management of natural Coastal, bulk of our information on soil fertil Boreal. crops. lower the The is medium- forest That of first but in Swan coarse-textured soil nutrient levels may limit forest productivity in Canada was range large, to soils of suggested (1962) materials by after Lafond (1958) examination and of leaf from red pine (Pinus resincsa acidic soils and soils with appreciable Ait.) stone [Moench] Voss) plantations near Grand1- The and boulder more textured The productive silts poorest gravelly 1971, content predominate. and tree sands soils clays are fine- (Lcwry 1975). growth or on occurs deep peat on (Page Lowry 1975). and Mere, from a volume exhausted forest three main site quality Stand ured area of above living ground). dominant age. is The to is be and of conventionally area tree age index, the it meas sterre at 1 .37 of stocking may be tionships between abandoned, growth growth (K) and Red to phosphorus 1965, appearance. (Lafond 1958, on abandoned has also nitrogen (P) been (N) when (Mg) pine Ontario respond could forest achieved magnesium to the soil 1965). and and was been agricultural mineral-deficient poor added by sands had were Gagnon farmland shown together and K fertilizers to with (Leech 1967) . the average height soil and site than that (Duffy desirable 1965); to keep latter constant when studying properties. m and glauca outwash plantations nutrients only potassium in (cross-sectional of Increased at a specified common influence therefore, age. Site quality is deter trees and by stand, stand factors on growth nay be less of derived governed density (index) basal mined by site of stand factors: density as wood The the practices produce of spruce (Picea Quebec. supporting with The white growth and rela soil-site General ements in readily insufficiencies soil, apparent deficiencies. have however, than are Fertiliser provided the bast of el are less extreme test plots evidence for assessing soil nutrient-supplying abil ity in itive relation growth to tree responses damand. in Pos fertilizer trials et in Scandinavia al. 1969) (e.g., and the United States (Gessel served as stimulus studies on forest. et al. to fertilisation These (e.g., 1974) a Carbonnier 1972, 1969) natural and Braastad others et al. were instrumental in establishing forest fertilization as an Age Canadian of experiments Moller FERTILIZER TRIALS northwestern operational Fertilizers fores try, in plantation have been nurseries, establishment, juvenile, immature used at and and in time of at the semimature stages of forest development. practice in these locations. Additions As early as the recognised as nn limiting growth mid-1950s, important of N was element Douglas-fir (Pseudotsuga msnziesii [Mirb.] in British Columbia (Crossin 1966). Reports by Weetman (1973) and (1973) indicated ran (1968), Nostrand that responses particularly N, be in erous forest. eastern and During the reviews year) early begun 1970s received Althen other up since these various interim (5- a number of fertilizer the late industry, 1960s and universities, forest op stock (van the of NPK on The basswood (Tilia red sandy oak (Quercus loam soils black walnut (Juglans nigra Even with weed competition ments have been published. Among these found studies, the produced no increase in foliar N, gram, example, Forest comprising experiments is 79 forest Manitoba, Ontario, by services of Quebec Brunswick and by Service in Saskatchewan Scotia. Some been data these objective of determine what can us its tell from the the about Forestry and Nova conclusions of height growth during the report is and over increased The of to and a 1975) jack P L.) of of placement in of P holes black ash (Fraxizus but growth. and a 10-year-old failed to Fertilization (Calvert pine (Pinus trees growth. planting leaves 5-year-old p and unfertilised white height Althen no improvement in concentrations and americana von fertilization first five years bottom walnut improve trials fertility the the influence on productivity of forest soils. concentrations In a fourth experiment, fertilizer soil broadcast at New experiments. these herbicides, that Alberta, analysis present K by and Canadian preliminary drawn from the Pro standardized established provincial have Inter- Fertilization and L.) on clay controlled for and L.) and both provincial and federal govern provincial of fer abandoned silver maple (Acer saccharinum loam soils. has von planting. were and on age results which broadcast L.) L.) nutrition of attention. on time planted americana the years reported experiments species rubra 10 little (1976) three were results. to realize nursery hand, to very at in by the forest tilizers published, of On of farmland initial to 1974). (1972) period results trials conif fertilizer required den Driessche 1963, Armson and Sadreika (1975) describe these their ware to could also natural Reviews by Rennie and Armson et al. trials Bhure of are timum production of Hoyt and fertilizers, realized Franco) et al. nurseries and Armson (Winston 1977) banksiana Lamb.) plantation likewise failed to stimulate height growth. Low per-hectare initially seedling- age from forest coupled with and demand sapling- accelerated nutrient release from the decomposition 10 of surface organic material carrying charges and large ularly on quantities of nutrient-rich cutovers, response to nay (Page 1974) slash, needles explain fertilizers partic and the by bark lack these of young years Additional fertilization of might be to addition 30-year-old forest2, a to immature jack 20-year-old rubens balsam fir (Abies plantation M natural (Picea a of red pine spruce Sarg.)-white balsamea are western triple [L.] Mill.) The results Canada stands fertilization either. responses by may this suggests not respond to Positive 15-year-old most commonly used urea as a source of for p N, and Nitrogen Response no effect that immature of for and hemlock (Tsuga and diam number potassium chloride for K. experiments growth, from forest greater the superphosphate heterophylla [Eaf .] Sarg.) forest3 had on are gain merchantable The fertilizers that spruce- (Timmer and Fisher 1978) 30-year-old 20- where increases that so semimature realized growth eter harvesting. The harvest, on investment could be minimized. trees forests. or so before growth Douglas-fir from in and the a the hypothesis limits the growth across United that of species. number of forest adjacent support coniferous large adult at The States lack of least N some responses of forest^ and 25-year-old western hemlock Douglas-fir (Webster et al. erally positive and often statistically 1976) were not tent with this generalization, In the latter response when to the study, additional fertilization was forest was consis however. realized thinned before fertilizers were applied. and significantly greater of unfertilized forest pine responded well Most fertilizer been growth natural trials, conducted in forest, usually relatively fully stocked, stands either of single however, semimature uniform, even-aged rationale mature for forest was to owr controls, to commonly fertile, deep, sandy fertilization. found These on increase loams. The responses serai- white yield also, but were not fertilizer Growth response spruce in higher balsam many trials are loam inherent fir generally statistically species sandy of were the clay results significant. commonly to associated loam fertility, tills tion—fifth Toronto, year unpubl. results. rep.). 3Rottink cited by Miller 1976. 4Gessel cited by Miller 1976. Univ. are compacted and of although therefore of restricted rooting. fertiliza and positive some (urea) less- loamy sands and gravelly of immature jack pine (Pinus banksiana nitrogen Jack Douglas- Lamb.) to growth fertilization whereas are These 1977. the largest volume of wood species with R.D. than gen coniferous fertilizing with a single application of were (Table 1). to attributable species or simple mixtures of conifers. The pine with the largest percentage increase in fir produced the have jack shallow and Black spruce showed the poorest response over all: in growth of a number of fertilized experiments, trees was than that of unfertilized trees. (1975) found black spruce with less Lcwry high site indices on fine-textured silts and clays and indices loams of with medium- and sands. the were spruce on balsam [tedium and and low coarse-textured Ihe results from some fir influenced by and spruce mortality stands and crown higher with ammonium nitrate urea (Braastad growth al. responses than with 1974). to urea Poorer have related to volatilization of N, hydrolysis of damage associated with a spruce budworm microbial epidemic in eastern Canada. N in humus. Nonuniform et urea to been delayed ammonia, immobilization of and fertilizer stand and soil conditions may also have contributed to nonsignificant responses in those increases Table 1. cases in which in volume were positive recorded. Five-year total volume coniferous forest to In Canada, response of with 224 kg N ha"1 as ureaa. produced does fertilizers fertilization comparison concentrations not show that one fertilizer other. Weetman higher and is et first-year tions of the two conclusively superior to al. (1972) foliar needle foliar K by N the found concentra weights with urea application to boreal black spruce higher foliar during the N first fertilization Acadian tions In three region first-year than did forest spruce, years the (Weetman et al. boreal Algar higher et produced concentra a and associated (Weetman N in despite after in nitrate urea but nitrate spruce foliar (Weetman centration nitrate ammonium black Ammonium higher pine of forest 1974). with jack 1974). foliar with al. con ammonium 1974), urea produced greater basal area increments, although the response was not signif icantly different from that produced by ammonium nitrate. superiority aData from 1976a, b, Gessel c; 1977; Weetman et Morrison al. 1976, et al. 1979, 1979 other, in of N-source of increased terms semimature Morrison jack et pine, al. b4 years Weetman and Algar cHean for site IV Douglas-fir increments dMean for site I Douglas-fir urea study, total Nitrogen Source years all Canadian volume-growth of N in almost experiments. increases (Pinus sylvestris L.) (1974). by produced noted by or In the first the volume two by In Sweden, Scots pine have averaged 30% than ammonium hemlock did nitrate forest inconclusive 1976). in gains nitrate basal area urea. with have results fer in the second, greater ammonium gains the 1977a) roarchantable produced clear growth of than ammonium nitrate after 10 years; greater the source and no over was (1976a, tilizers were identical; third, Urea was Likewise, one in the produced over three Comparisons urea in likewise (Webster of western produced et al. These though North few in American number inconclusive in results, the superiority that has been of studies, and somewhat do not support demonstrated required this important question of of Peak growth responses Sweden. 1973, resolve (Weetman or Lee 1974) 1971) third foliar have been correlated creased needle nutrient concentrations Weetman and of addition could needle tion of response be that without 1973, and and such of following year—this young with the 1973) or seasons studies. (1975) lished results to control of ha~' red levels within fertilization of urea-N spruce to 3 a et after similar centrations untreated Douglas-fir concentrations do and more late and Within 2 10 indicate urea is years of that most initial indication of when the 1960s K of on response the will the 10-year trials initiated and early 1970s are The optimum maximum growth amount of above those jack data), and 4 balsam Gagnon 1971) . of urea-N 45-year-old in trvo mature other Weetman after a in 448 control N of likely to occur the in kg The therefore response the to 4 years after fertilization. ha~1 (Fig. eastern conifers of age: black 1971) and balsam fir spruce 1) . semi- (Weetman (Gagnon 1973). Phosphorus and Potassium Response an forest 1975) . analysis 200 kg for jack 1975) foliar years in pine stand was a This rate produced the optimum response (Vfeetman foliar these information of and unpub pine ha~1 addition, foliar levels were still results p reported. Growth response been reported after when con after those tenth in these to fertilization, magnitude spruce, than some response tions higher to (Morrison, Although available the pine N give of addition of 112 kg urea-N ha"1 to black whereas indicated for 1977) foliar increased for seventh was jack reineasurements in growing a sustained with (Lee recorded kg eighth and rate, unpublished and years 300 reported al. in (Truong-dinh-Phu 3 to 1978). remained fir (1971) to Pienaar fertilization forest (Morrison, 2 100 been (Salonius years at have (Safford white spruce urea with occur and the with considerably be in foliar-N concentration in data). duration growth applica not A somewhat similar effect has added length Declines into to by rapidly N did 1975) growing seasons were jack pine. higher seventh response predicted (Miller (Weetman second general declined response fifth trees, concentra height until spruce the in responses With peak noted increased nutrient tions, black was tests—and been Armson increasing the fertilizer by fertilisation weight foliar If to made With Calvert reported and in (Krause assessment parameters. however, with 1974). hold, duration needle weight Algar correlations fertiliza- and occurred in thereafter. tion to 100 - 150 kg N to source of N. after is N applied. in agreement increases response ha~1 by Douglas-fir (Miller and pienaar Length of Response Growth growth the quantity of nitrate ammonium Further studies are Duration dependent on to first 2 1973, of P and van K on for mineral soil black Nostrand mixed spruce-fir to single applica spruce and Bhure 1973) (Krause 1973). have (Krause and Balsam fir in New Brunswick responded to K but not to there N and was coefficient a P (ibid.). significant for the Furthermore, correlation relationship between foliar K in current needles and basal area spruce growth. Red pine plantations abandoned on from responded well and white outwash sands agriculture to have fertilizers, partic When P additional and K were growth (TUble 2), added was with often N, realized but generally responses were not significantly greater than when K ularly K, producing 25 to 80 m3 ha"1 of alone was extra wood over 5 K fertilizers produced the best average response et al. 1959, et al. 1976). the responses than the supports element erous to 10 Leech of (Heiberg 1967, Gagnon In the other experiments Black to plus P and response the years 1965, to hypothesis priroa K were N, and that importance N lower this is to used. in A combination of N and jack pine and was most responsive spruce balsam fir. to N P and white spruce to N alone and N plus P. the conif forest growing on mineral soils. Lack related ment of significant partly to replication Furthermore, response insufficient in these many is treat experiments. results are derived mainly from experiments in which one or rarely was more added response yields than one with surface might level N. be If were of K an or P optimum developed the improved. An further example of a response surface for N-P-K application 6o a to jack pine in Ontario is presented in Figure 2. Species-Site Interaction 4 tr Species-site LLJ tion 2- to tree nutrient supply in demand makes it soil difficult ID the role of soil fertility and response fertilization. species 200 4DD APPLICATION LEVEL | kg N/ha) Figure 1. Five-year An differ in example their requirements is presented which shows the nutrient four species a sandy loam till. There growing on developed was a respect of to hew nutrient in Table contents 3, of the same soil, from calcareous considerable dif growth- ference over-control of 45-year-old between jack pine the aspen (Populus tremaloides Michx.), tion to level errors) al. volume with to draw to conclusions rela and a o- firm interaction nutrient forest urea (means from 1976c). in rela in nutrient species despite application white similar dry-matter contents. Morrison eL spruce tity (Ca). the nutrients, Jack high pine nutrient fact that jack pine forests accumulated of particularly every and the ± standard spruce accumulation greatest and demand did quan exhibited for accumulated than had Aspen and a calcium less the of other Table 2. A summary of total volume fertilizer3. response to combinations of N, P and K aData from Foster (unpublished); Hoyt 1973; Krause 1973; Morrison et al. b, 1977b; Morrison and Fester 1979; van Nostrand and Bhure 1973; 1976, 1978, species. 1979. Black and balsam fir, spruce, white spruce growing in a northern Ontario mixedwood forest on an upland till, did not respond to N and P, whereas white birch in the same stand responded (Morrison well and Foster A soil adequate be may therefore nutrition deficient others. for some in provide in mixture, fertilization (Weetman et al. for pine responds better 1976, than spruce 1979). Data from 27 separate fertilizer trials in urea-N was ha~1 jack inverse used to forest at response greatest index. to growth the The 112 show relationship associated with site pine applied were index and The there site were III wise is questionable, only a forest. found an because few observations Gessel (1977) inverse between site response to application index in like relationship and Douglas-fir of 224 and 448 in or a which 224 site (Table increases stands of validity kg general between N trials in Oregon and Washington. species, nutrients Where black spruce and jack pine occur to relationship kg urea-N ha"1 in a study involving 200 1979). but 1976a, Weetman et al 4). were lowest of the Using height/age as an index of is attractive because tree height site growth stand is relatively density. site independent index, of however, interprets all the patterns of growth that the tree experiences during its lifetime, and thus may not reflect how the tree is alternative growing might be at to present. use An diameter growth to assess current growth rates, but the inverse relationship between diameter growth and stand density is a drawback. Chrosciewicz (1963) reported that jack pine site indices based on breast height diameters varied in a way similar to those based on heights, when ra az o Figure 2. Effect of volume growth-over-control of 55-year-old phosphorus Harriaon et al. 1976a). and potassiun with nitrogen on 4-year jack pine (data from Table 3. Dry matter and nutrient content (kg ha"1) of 40-year- old forest on a sandy loam soil developed from calcar eous till.a Species Dry matter aspenb 166 800 red pineG jack pinec 199 400 147 300 white sprucec N P 457 150 800 67 449 64 421 296 50 30 K Ca 367 1074 205 119 335 241 254 Mg 76 809 46 72 46 aData are from Alban et al. 1978. ^Natural forest. cPlantation (1 Table 4. Five-year response x 1.5 m spacing). volume to growth-over-control fertilization with urea. (m3 ha"1) of jack pine in (mean with range in paren theses )a Site classb Treatment III (kg N ha"1) (11 m - 13.6 m) 112 8.3 (5.8 - 12.1) 224 13.1 (9.7 - 19.1) u (13.7 m - 16.7 m) 6.2 (1.6 - 15.9) 8.7 (0.9 - 17.8) j (16.8 m - 19.8 m) 4.8 (-.8 - 10.4) 6.7 (-2.7 - 17.8) aData from torrison et al. 1976a, c, Weetman et al. 1976, 1978, 1979. bPlonski 1974. 10 sampling was fully response to fertilizer umented, and restricted stocked stands. Since to most fertilization toward sites that of tion. In as contribution that soil current or periodic annual increment), diagnosis make toward which sites trials have fully stocked current located stands, volume may tionship be by black uniform use (measurable both diame ter justifiable. between measured in the growth integra tes height, and been spruce A stand current and annual the can with best to following soil doc those fertiliza section and fertility the foliar identifying problems and a potential to respond to fertilization rela vigor respond is identifying as will be examined. increment foliage-N IDENTIFICATION OF MINERAL DEFICIENCIES concentra tion has been demonstrated by Lowry and Avard (1968). spruce As mos t experiments the black published of were Foliar Analysis Deficiencies located in site class I forest (Plonski 1974) a comparison response to jack For Therefore, response pine annual site as of a we pine not be morphological generally the intensively and chemical of 50 spruce periodic (Table the 5). slower- ularly in which to managed analysis valuable appear nurseries forest. has aid juvenile plantations. southeastern diagnosing With (PAI^q 2-3.9) showed the to best to Ballard and Pritchett (1975) "foliar soil tilization. or both levels of fer Stands with a PAI50 of 6.0 the two range for predicting as for southern better appear to be a poor risk for fertilization. in volume result of examples was a of good were (Table (Table 5) . studies are suspected wide produced fertilization, responses classes There increment however, responses noted 4) and all to site/growth a and foliar In plantations, production classes placed rate these response and on the optimized, and results from experiments we are unable numerous to determine and total used to marine whether or not a forest will respond to from agriculture fertilization. positive dinh-Phu response icant The number of responses and the magnitude to pine are fertilization, and Douglas-fir encouraging effort toward surface so that and response justify defining the of particularly the maximum jack to N, continued response potential (1975) and between (r2 also positive site of index r2 = .5). (basal area white linear and spruce abandoned .6). found of K and Mg in red pine a relationship sands = multiple demonstrate significant on high Truong-dinh-Phu volume) plantations a therefore between foliar K and growth Despite with effective." is have analysis and are procedures is soil. (1975) correlation more stocking that requirements increased, the testing plantations nutrients Gagnon positive relationships. is States, state used fertilizer pine analysis for and and reference United commonly site additional validate most poor demand PAI50 Therefore, required and in analysis partic nurseries growing forest response a in in are and Foliar been nutrient deficiencies the observable abnormalities restricted spruce function and and compared black increment at age both index fertilization would possible. volume of Truonga signif correlation concentrations foliage (for K, 11 Table 5. Annual volume growth-over-control (m3 ha~1 yr"1), over 5 years, of jack pine and black spruce in response to fertilization with urea as a function of pai (m3 ha"1)a. aData from Foster (unpublished); Morrison et al. 1976a, b, c; Weetman 1968; Vfeetman et al. 1976, In natural, forest, severe unmanaged, patterns of foliage and mature deficiencies usually observed. are not Because of seasonal nutrient concentration within-crown in variation related to age and position of needles, particular care must be exercised in the selection of foliar materials (Lowry and Avard 1969, Morrison 1972, Ellis 1975). procedures When are rigid followed, sampling differences between good and poor grcwth have been correlated with foliar nutrient con centrations. For example, significant positive growth linear as correlations indicated by site between index and the N concentration of black foliage have been reported by (1964) and Webber (1974) Lowry found and Avard spruce Gagnon (1968). that N in current foliage of Douglas-fir was signif icantly related to site index. These results also support the hypothesis that there is a general N deficiency in northern coniferous forests. 1978, 1979. Swan (1970, 1971, 1972, etc.), by solution culture, estiaiated critical foliar level of macroelements for various coniferous species. To aid in diagnosis of nutrient deficiency in mature forest, he adjusted his pot- culture derived indices to concentra tions of nutrients normally found in adult forest. Since a number of fertilizer trials have reported both growth and pre-fertilization foliar nutrient concentrations, it is now possible to determine whether Swan's foliar indices can be used to prescribe fertilizers (Table 6). On the positive side, a response to N or to N and P was predicted in black spruce and demon strated in two Moreover, no predicted for response was by jack by response noted. experiments. to in The diagnosis to p was pine noted. was and response however, one K species and despite the foliar deficiency three either pine, predicted, tion of response no to was n not identifica of an acute experiment, no 12 aOata from Foster (unpublished); Foster 1979; Morrison et al. !977a, b; Morrison and van Nostrand and Bhure 1973. bSwan (1970) cSignificant at For may several be not of example, correspond luxury the the can inter nay physiological tree consumption trees the of because a respond of nutrient, to nutrient stress by an internal translocation of elements from older since they to years. 7 retain various tree species knewn. concentrations. concentrations with of difficulties with foliar foliar requirements ftlso, reasons, encountered pretation For .05 or better. With indirect (e.g., texture, may be as Rapid needles decline for in In 3 con may be abscis the exceptions 1975), testing, important may to Pinus which are well adapted to soils matter and be spp. lew in exchangeable nutrients. is nutritional difficult soil nutrient because requirements of and pertains to for to many of adequate to measure the the for the soil no assessing nitrogen (1977) commonly the Leaf, have our not tree of N In to cur observation that accepted active supply..." particularly relevant. and 'available to nutrient." importance Tamm's Canadian extractants fraction of soil "[w]e have the tree to researchers procedures the few to different applicable soil a statement on soil it species, of with According developed, forests, the is "[florest view So 1 Nutrients regime soil tests Ballard and Pritchett (1967) States species, trees' Assessing assessing chemical place, although conditions. Translocation first (e.g., in organic seepage waters) in direct Leaf's United particularly soil layer, currently in use. sion (Turner and Olson 1976, Miller et al. 1979) and a concurrent reduction growth. fertility humus of useful fertility soil naterials, of or absence as fully knowledge, to current tissue, their centration in older needles followed by premature needle tree of parent nature presence not yet current measures soil are cur method fraction is of also 13 Second, forest the soils heterogeneity and the of considerable extent of a tree's rooting system, both horizontally and vertically, pose particular problems with respect to selecting samples of soil for chemical analysis or for bioassay study that are representative of a forest's rooting zone. Third, because forests have a long life, the potentially nutrient supply. m particularly coniferous the boreal for forest, the thick raw humus layers are espe cially important to tree nutrition. Although considerable information has been obtained on humus chemistry (Bernier 1960, Bernier biology and and Roberge 1962, Weetman 1962), partic ularly the reactions of fertilizers in humus (Knowles 1969, Salonius 1972, Roberge 1976), the role of humus in tree nutrition is still not fully understood. Fourth, a tight cycle of nutrients is maintained between the trees and the surface soil so that release from humus provides a forest's nutrient requirement, ularly considerable part for mobile elements Mg (Miller et al. P are 1979). organically of the partic like K and Nitrogen and bound and are released very gradually from slowly decomposing humus. Accumulation of humus during the midlife of the forest is considered the cause of the general insufficiency of N in the northern coniferous forest (Weetman 1962). Fifth, p uptake into trees is facilitated by mycorrhizal associations with trees. This further complication values of available chemical tests. coniferous symbiosis is a in interpreting P derived by soil mosses have a particularly role in the forests. cepted from nutrition of dustfa.ll are Nutrients rainfall and inter released more rapidly from decomposing mosses than from litter (Bernier the decaying and Roberge tree 1962). Adventitious rooting within the humus and moss layers allows black spruce trees access available nutrient-supplying power of the soil is as important as the readily soluble ests, Sixth, important to these nutrients. Because many of these factors and others must be considered in the evaluation of soil fertility, one would e^ect great difficulty in and measuring parameters that can be correlated selecting of fertility with forest productivity. Heger (1971) found that 11 classes of drainage and parent materials were of no value in explaining differences in white spruce site index in Alberta. Soil properties, ing factors however, directly or includ indirectly reflecting soil nutrient regimes, been closely correlated with productivity with site of Arneman 1961, 1975). a site, index and (e.g., usually pawluk Wilde et al. The importance have the 1964, and Lowry of keeping age and stocking of a forest constant when soil-site relationships are sought was emphasized by Duffy (1965) in reports on the influence pine (Pinus of site on contort* L.) in The studies of Wilde et al. Pawluk and demonstrated lodgepole Alberta. (1964) and Arneman (1961), which that jack pine production was related to soil fertility, were conducted in fully stocked natural stands of similar age or in ewn-aged plantations with controlled stocking. The considerable matter production and within a species is range nutrient in dry- content demonstrated in Table 7 in a comparison of three 40- to 14 Table 7. Dry-natter and nutrient content (kg ha"1) of 40- to 45-year-old jack pine forest. Dry Site class aAlban et al. Mg Ca K matter Trees ha 1978. Morrison and Foster 1977. ^acLean and Wein 1976, 45-year-old different jack soils. quality and edly pine ited by density for climatic contribute to the As an example of between were important jack Ontario. he and and site, found that regional moisture regime, soil petrography all to the pine growth forest of in fully northern that were the highest pine associated with site siliceous soil materials containing 30-40% basic particles and that dimi nished when the site indices content of such particles decreased to less than 10%. Lowry in (1975) relation natural black Canada. growth was often and deficient Ca and Mg on were The amount of an absorbed by a plant factors other than element is that is influenced soil by fertility, including interactions between elements both inside and outside in is particular moisture. A the plant, dependent lack of on and soil correlation between soil foliar nutrients and site in a s tudy by Douglas-fir was other soil than Webber (1974) related to nutrient with variables parameters affecting tree metabolism. With regard to soil fertility found indices nay also the complex relation soil texture widely P sites, deficient on organic soils. and differences. growth conditions, wetter exhib these three variables tree macroclimate, site yield As yield (1963) soil stocked in undoubt Geographically separated, Chrcsciewicz from patterns these forests. are are the accumulation forests ship forests Differences stand responsible nutrient 1977. He over studied to site spruce found a site index stands that broad N in factors in limited range 125 eastern of tree site Where moisture and temperature limiting forest productivity, soil fertility by fertilization is likely to increase tree growth. (1974) emphasizes investigations are to tion useful that, soil in evaluations, ducted of be on within moisture a well if forest regimes. future In status fertiliza must defined not Webber nutrient they are improving be con framework other words, there is an urgent need to stratify our sites by means of a site classifi- 15 cation system with a strong emphasis on nutrition and moisture so that we can identify those sites that will respond to fertilization. results of a large number of fertilizer trials across Canada support the generalization that N is the most important element limiting the growth of coniferous forests. Growth respon ses to p and K have been reported, but only in combination with N. On many of the coarse-textured less soils, fertile, jack dry, pine and Douglas-fir forest respond well to H or N in combination with P and exist. K. progress of has nutrient that more on the the best volume poorer sites, vigorously tested been growth a wider may sandy doned loams from response loams the juvenile the level that sufficient early aban hardwoods indicates contain support clay agriculture, of fertilization soils and growth of of to these nutrients to newly established forest. The average fertilizers spruce, balsam response red fir by by growth western spruce, has hemlock, black been pine response less and the use detecting trees. The sampling has for some levels species have been published. Although present foliar diagnosis may be useful for detecting severe deficiencies, the technique needs to be more fully developed before it can be used for prediction purposes. LITERATURE CITED Alien, D.H., Schlaegel, and to white spruce and than the Douglas-fir. Information relating response-tofertilization to nature of soil mate rials for these species is needed so Perala, D.A. and B.E. 1978. Biomass nutrient pine, distribution and the same soil spruce in stands on type in Minnesota. Can. J. For. Res. 8:290-299. be required not only to enhance growth cut also to prevent the development of serious nutrient deficiencies in trees. On and foliar aspen, fertilizers in foliar developed On coarse-textured soils abandoned agriculture, for toward for deficiencies critical range of site indices. from can be problems A should be over diagnosis methodology and site index for these species, indi cating fertility been made foliar suspected relationship between response occurs combinations where Soil chemical analyses useful for predicting response to fertilization have not been developed. Considerable WHERE ARE WE IN SOIL FERTILITY? The that species-site identified Anon. 1976. Glossary of terms in soil science. Ottawa, Armson, Can. Ont., Publ. K.h. Forest and tree ment and Min. Dep. Agric, 1459. 44 p. Sadreika, nursery V. soil 1974. manage related practices. Nat. Resour., Toronto, Ont. Ont. 177 p. Armson, K.A., Krause, Weetman, G.F. tion response coniferous B. Bernier Forest forst. and soils H.H., and 1975. Fertiliza in the northern p, C.H. and 449-466 in Winget, Ed. forest land management. Proc. Fourth North Am. For. Soils Conf., Laval Univ., Quebec, Aug. 1973. l'Univ. Laval, Les Presses de Quebec, P.Q. 16 Ballad, R. and Pritchett, W.L. 1975. Evaluation of soil testing methods for predicting growth and of Pinus elliottii fertilization. Am. Proc. Bernier, B. netabolisme Rech. 42:265-284. Duffy, Observations sur le de quel- de Fonds l'Univ. Contrita. No. 5, Laval, 44 p. B. Etude and in tion de humus de Roberge, vitro sur H .R. 1962. la mineralisa 1'azote organique dans forestiers. litieres Rech. Influence forestieres. For. Quebec. I. de les Fonds 1' Univ. Contrib. No. 9, Lava 1, H., growth H. increase tion. R. 1974. The after and volume fertiliza Foreningen the Dep. Ellis, Skogstrads- pine Can. to J. 124-138. and ftrmson, nitrogen K.A. of and For. Res. section Ottawa, contort a Engelm.) of Ont. in Alberta. Publ. No. 60 p. R.C. 1975. Sampling deciduous broadleafed trees mination of leaf weight and foliar elemental J. For. for the deter concentrations. Res. Can. 5:310-317. F. 1975. young jack phosphorus. and Lowry, 1970. For Ill Volume estimation prediction of and black volume growth spruce through relationships. Inst. Can., s tand- Pulp Woodl. Pap. Rep. 26. p. Gagnon, J.D. between 1964. site nitrogen mature 5:529-538. G.L. est soil-site studies. 31 R.A., pine (Pinus For., battring. The growth response Chron. Relationship var. latifolia foothills Res. Calvert, 1965. lodgepole Dougl. foradling Institutet for SkogsforArsbok p. For. 47 p. Friberg, Gustavsen, Island. P.J.B. Evert, Braastad, and A progress between site factors and growth of 1065. Eernier, J.A. 1966. report on forest nutrition studies on Vancouver Soc. forestiers. For. Quebec. Marlow, G.L. Sci. Soil respiratoire humus E.C., Ainscough, phosphorus to 39:132-136. 1960. ques response Crossin, at Relationship index two black and crown spruce. foliage levels For. for Chron. 40:169-174. Carbonnier, A., C, Ebeling, Holmen, 1969. H. and Godsling fastmark. mineral F., Tamrn, av K. LantbrAkad lidskr. C .0. Gagnon, J.D. site on northern Ottawa, 28 p. 1963. jack and forest on on a 20-year-old Skogs 0. tion. For. red Chron. magne fertilization pine planta 41:290-294. 5:236-246. The effects of pine Ontario. Ont. Effect of potassium sium Gagnon, Chrosciewicz, Z. 1965. pa skog (Fertilizing ground). Hansson, Publ. growth in J.D. 1973. fertilisation croissance Dep. For., baumier. No. 1015. Foy, 24 p. P.Q. en Effets azotee rayon Serv. Rapp. can. Inf. de sur du for., la la sapin Ste- Q-F-X-38, 17 Gagnon, J.D., Conway, H.S.D. J.M. 1976. and Growth Swan, response following fertilizer application in the Grand'Mere plantations. For. Chron. Gessel, 52:53-56. S .P., K.J. behavior of T.N. 1969. growth Douglas-fir with fertilizer Washington. Inst. Gessel, S.P. ship to given at L. 7, tionships Alberta Prod., Congress, spruce mixedwoods. 15 p. planted at various spacings on site. a For. 5:142-153. Growth increases after fertilization in mature jack Nat. TR3-73. Rescur., 81 K, 1, 24 p. Mg and S defi and p. 88- fertilization—the practice. Symp. Proc. V.J. 1971. Effects of urea fertilization on nutrient con centration of needles and soils in thinned and unthinned Douglas-fir stands. Serv., For. Br. N.B. Publ. p. Dep. Y.J. B.C. of stand a 25-year-old to thinning and urea fertilization. Leech, For. Rep. Four-year basal area response Douglas-fir Res. Can. Inf. 25 p. 1974. growth Environ., Victoria, BC-X-55. Can. j. For. 4:568-571 . R.H. red pine and balsam fir stands. Dep. Lee, Lee, Influence of potassium level on red pine 1973. Contrib. No. 1967. Fonds 1 ■ Univ. Ala. Dep. H. 1959. fertilizer J.S. ory in Heiberg, S.O., Leyton, L., Loewenstein, Hoy t, Laval, de 122 in Forest For. Serv., Ottawa, inf. Rep. FMR-X-32. Sci. For. a.l. 22 p. potassium-deficient Rech. Tenn. Valley Auth., Muscle Shoals, white Can. glauca ciencies in forest trees. Site index/soil rela for Environ., Leaf, Seattle, IUFRO Austria. resi'iusa afc Pfessa Quebec. 119 p. 1977 1971. Ont. For. 1977. Site in relation forest tending. Paper Ossiach, Heger, in western Washington, No. and The nitrogenous Univ. Pinus dans la province de Quebec. Stoate, Turnbull, Contrib. Lafond, A. 1958. Les deficiencies en potassium et magnesium de quelques plantations de pinus strobus, 1965. pine slopes. Res. Rep. Fertilization plantations Ont. No. Dep. 68. Leech, R.H. 1967. red pine on a on of sandy Lands For., 113 p. Fertilization of sand plain. Ont. Dep. Lands For., Res. Rep. No. 72. 53 p. Knowles, R. 1969. Microorganisms and nitrogen in the raw humus of black spruce forest. Trend 15:13-17. Krause, H.H. 1973. Forest fertiliza tion in eastern Canada with emphasis on New Brunswick studies, p. 188-205 in Forest Symp. Proc. USDA Rep. NE-3. tion. Serv., Gen. Tech. fertiliza For. Lowry, G.L. 1975. Black spruce site quality as related to other site conditions. Soc. Am. Proc. soil and Soil Sci. 39:125-131. 13 Lowry, G.L. and Avard, Nutrient content needles. II. crown class Inst. p. Lowry, of black spruce with relationships yield. Can., 1968. Variations and growth and P.M. Pulp Woodl. Pap. Pap. to Res. No. 3. 20. and Nutrient Avard, content jack P.M. of pine black variations ommended sampling Pulp Pap. Pap. No. Res. 10. 1969. spruce needles. Seasonal D.A. Biomass Ill. and rec procedures. Inst. p. and of hardwood Hew 1972. Can., Woodl. Wein, jack stands Brunswick. R.W. pine in J. mixed For. Res. Morrison, I.K. in in northern For. Res. Morrison, borea1 Morrison, I.K. in New For. Res. H.G., J.D., succession Brunswick. For. J.M., Pauline, Nutrient cycles adaption Can. Miller, O.J.L. in pine to poor Res. 1979. and their soils. Can. J. 1976. Effects of fer tilization on mortality in western hemlock p. and Univ. For. Miller, Douglas-fir 253-265 in Hemlock Proc. Management Washington, forest Douglas-fir Pap. N.W. and in Lake Am. 1979. Dep. exper spruce-fir the area of Black northern Environ., Sault Can. Ste. Report O-X-299. I.K., N.W., Marie, 15 p. 1976a. Lamb.) in to For. PNW-165. Exp. and Foster, lUcker, Fertilizing northwestern results. Can. semi- (Pinus banksiana For. Ontario: Dep. Fish. Serv., Sault Marie, Ont. Report I.K., Swan, H.S.D., O-X-240. 42 p. Conferences, USDA L.V. 1973. nitrogen 24 p. Ste. F., D.A. mature jack pine N.W. USDA For. Serv., Hegyi, Winston, T.L. Morrison, Seven-year response of 35-year-old Northwest Soc. stands, Seattle. and Pienaar, tilizer. Foster, Serv., Ont. Western of Serv. R.E. banksiana Sci. spruce fourth-year 9:19-26. R.E. 1977. fertilization in Environ., Miller, N.W. 7:562-578. Cooper, and J. growth in two nitrogen- phosphorus Morrison, Miller, Can. Pinus Soil and Five-year For. J. of stands 41:441-448. Ontario. patterns Ontario. fores t jack R.W. and hardwood pine 3:170-179. stand. Nutrient accumulation for postfire pine for 50-86. components jack I.K. and Foster, Sturgeon Wein, p. Fata of urea fertilizer added to a upland and aldre Distribution of aerial natural 1977. D.A. 1972. elements iments 6:441-447. MacLean, av Arsbok Inst. 1976. and northeastern Can. Analys Skogsforbattring 1971. Lamb, 54. Tillvaxtokning genom godslingsforsok. J. MacLean, G. godsling. several G.L. and Moller, fer Pacific Stn., Res. and Winston, ■ten-year growth tilizer of spruce stand Ontario. a For. Foster, D.A. response 1976b. to 90-year-old in Chron. fer black northwestern 52:233-236. 19 Morrison, i.k., Winston, D.A. and Foster, N.W. 1976c. Urea dosage trial in semimature jack pine for est, Chapleau, Ontario: Rennie, fifth- Can. For. Serv., Sault Ste. Marie, Report O-X-251. Morrison, I.K., N.W. Swan, H.S.D., Winston, D.A. and Ten-year pine Ontario. Morrison, a in Foster, semimature Winston, N.W. D.A. 1977b. fertilizers on growth of of Ontario; Dep. fifth-year Environ., Sault ste. O-X-258. Page, G. Marie, common results. For. Properties Newfoundland their growth. forest relation Can. J. For. some soils to forest Res. 1:174- G. 1974. on Effects of the properties Newfoundland forest forest of soils. some stn., 27 p. Life Univ. P.O. of organic Agric. Bull. Microbiological fertilizer organic forest treatments soils. Soil 11.4:12-19. coated For. Sci. Maine. 1972. to urea plantation. Swan, Serv., Publ. S. No. and 1332. Arneman, in Efficiency of from plastica Dep. white spruce Environ., Ottawa, Can. Ont. Bi-mon. The mineral pine growth. w.L. tables Resour., (metric). Div. For. Normal Ont. Min. of Pap. Res. the Grand'Mere Res. inst. Index, Can., Pulp. No. 131. 14 p. 1961. For. Sci. 7:160-173. 1974. 1962. plantations. 32 p. H.F. H.S.D. nutri tion Dep. Some forest soi 1 characteris tics and their relationship to jack Plonski, effects H.E. and Knight, Salonius, P.O. 1978. nitrogen recovery Environ., Can. For. Serv., Ottawa, Pawluk, the Res. Notes 34:23-24. coier Ont. spruce. Exp. 740. Sci. 192. Page, 27 p. soil-surface Young, red in Report of on response Serv., Ont. urea the at Respiration rates determining Salonius, 12 p. 1971. and Can. serai- Chapleau, gi\en Congress, T.W. 1977. Effect of soil and urea fertilisation on foliar nutrients and basal area growth of nitrogen, phosphorus and potassium mature jack pine forest, 1976. for Safford, L.O., and Effect Paper Forestry horizon of a black spruce stand. Can. J. Microbiol. 22:1328-1335. 1977a. northwestern World Roberge, M.R. For. Chron. 53:142-146. I.K., Foster, in stand Forest fertiliza Buenos Aires, Argentina. growth in two fertiliza tion ej<periments jack 8 p. 1972. Vllth year results. Dep. Fish. Environ., Ont. P.j. tion in Canada. yield Nat. Swan, H.S.D. between 1970. nutrient Relationships supply, growth and nutrient concentrations in the foliage of black spruce and jack pine, pulp pap. Res. Woodl. Pap. No. 19. Inst. 46 p. Can., 20 Swan, H.S.D. 1971. between nutrient Relationships supply, growth and nutrient concentrations in the foliage of white Pulp Pap. Res. Rep. 27 p. Swan, 34. and red Inst. spruce. Can., Wbodl. H.S.D. 1972. Foliar nutrient concentrations in lodgepole pine as indicators status and of tree ment. Pulp Pap. Res. Woodl. Rep. 19 p. Tamm, C .0. 42. 1977. primary - in Sci., V.R. Dep. Grcwth and response For. short-term Ecol. to Environ. 1978. aerial forest Environ., Ottawa, Nostrand, 1973. Ont. spruce la 1975. Res. Potassium deux elements croissance rouge au en Can. du pin J. For. von Althen, at F.w. improve growth lings. Dep. Sault B.D. Nutrient-growth plantations J.D. 1975. relationships Grand'Ms re whi te before fertilization. J. fir and Can. J. after For. Res. Olson, P.R. 1976. relations in a Douglas- plantation. Ann. Bot. 40: den Driessche, experiments Commonw. on Ont. and three Dep. Victoria, foliar for different Environ., Can. B.C. For. Report 19 p. S.R., Debell, and D.S., Atkinson, 247-252 in Hemlock Wiley, W.A. Proc. 1976. of Management Washington, Western Conference, Seattle. USDA Serv. Weetman, G.F. tions 1962. in a Nitrogen black inariana Mill.) rela spruce (picea stand Pulp Pap. Woodl. Res. Weetman, subject G.F. with For. Rev. 1963. Nursery, Douglas-fir. 42:242-254. 1968. of stands. to Inst. 129. Can., 112 p. Pulp Weetman, The nitrogen ferthree black Pap. Woodl. Rep. No. G.F. 1971. thinning nutrient Pulp Pap. R. Res. Index No. tilization quality 1185-1193. van Soil Serv., Can., and For. in spruce 5:640-648. Nitrogen Can. Marie, 13 p. sites. ments. Truong-dinh-Phu and Gagnon, Turner, Ste. to seed relationships Douglas-fir p. fails hardwood Environ., 1974. nutrient K.N., 20 p. Fertilization of Report O-X-249. Webster, John's, planting Serv., Webber, St. 1976. of in Environ., Rep. N-X-95. time black various fertilizer and soil treat 5:73-79. the Dep. Serv., Inf. N.D. of fertilization For. Nfld. Enure, et limitant hauteur Quebec. to Can. For. magnesium: and response Newfoundland. Univ. Bi-mon. Res. Notes 34:13. Truong-dinh-Phu. R.S. Growth BC-X-100. R.A. Dep. Serv., Univ. 4:53-59. Fisher, fertilization. Can. boreal Swed. Res., Open Lit. Publ. Timmer, Can., lim ting the long-term and considerations. Agric. require Inst. Factors production forest nutrient fertilizer van Pap. No. and 28. Inst. 45 p. Effects growth upland Res. Res. 6. fertilization uptake, of spruce Inst. 18 p. and black Can., of on wood spruce. Woodl. 21 Weetman, G.F. 1975. response of Ten-year grcwth black spruce to thinning and fertilization treat ments. Can. J. For. Res. 5:302- 309. Weetman, G.F. Jack and pine Algar, nitrogen D. fertilization and nutrition studies: results. 1974. three-year Can. J. For. 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Environ., Can. For. Serv., Ottawa, Ont., G.F., V.R., inf. Rep. DEC-x-8. 27 d. Krause, and Hoyt, H.H., j.s. , 1974. Some fertilizer response data for the Maritimes and parts of Quebec. P. 77-82 in Proc. of a workshop on forest Dep. fertilization Environ., Sault Ste. Rep. Can. Marie, in Canada. For. Serv., Ont. For. Tech. 5. Wilde, S.A., Weetman, G.F., E. Weetaan, Iyer, Trautmann, K.G. (Pinus J.G., Tanzer, C.H., w.L. 1964. and Growth Watterson, of jack pine banksiana Lamb.) planta tions in relation to fertility of non-phreatic sandy Sci. 98:162-169. Winston, D.A. diameter 1977. grcwth soils. Height response 10-year-old jack pine and fertilization. Can. For. Serv., Soil and of to thinning Dep. Environ., Ottawa, Bi-mon. Res. Notes 33:34-36. Ont.