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ADVID Technical Notes 1 THE GRAPEVINE MOTH Series: ADVID Technical Notes Technical Note 1 - “The Grapevine Moth” PUBLISHING DETAILS Publisher: ADVID - Associação para o Desenvolvimento da Viticultura Duriense Text: Cristina Carlos Photographs: Cristina Carlos / ADVID Coordinator: Fernando Alves Year: 2012 Print run: 250 copies Distribution: ADVID - Associação para o Desenvolvimento da Viticultura Duriense ISBN: 978-989-95481-4-5 Reproduction is authorised provided the source is acknowledged. We would like to thank Prof. Laura Torres (UTAD) for her revision of the text. Graphic Design: www.hldesign.pt THE GRAPEVINE MOTH 3 Contents m Introduction m Morphology m Biology m Damage and Losses m Risk Assesment m Integrated Pest Management . Cultural Precautions . Chemical Control . Mating Disruption m Biological control m Bibliography ADVID Technical Notes ADVID Technical Notes 4 Introduction The grapevine moth, Lobesia botrana Denis & Schiffermüller, is considered the main vineyard pest in the Demarcated Douro Region (DDR). The moth’s economic impacts arise not only from the direct damage caused by its larvae, but also from indirect damage due to the onset of rot, particularly grey rot. This publication is intended to provide practical guidelines that may support decision-making strategies for phytosanitary protection against the grapevine moth, taking into account the conditions of the Demarcated Douro Region. Morphology Adult Greyish-brown moth, 11-13 mm long, with a wingspan of approximately 6 mm (Photo 1). Eggs Elliptical, less than 1 mm, translucent to yellowish (Photo 2). At the end of its development, a black dot (corresponding to the pre-hatching stage of the larva; “black head”) can be observed. Photo 1 – Adult Lobesia botrana Larvae Greenish to greyish-brown, with a light brown head. Larval size varies from 1 mm after hatching to 1 cm at maximum development, and the larvae pass through five developmental stages. When disturbed, they make fast and agile movements, dropping from silk threads (Photo 3). Pupae Although difficult to locate, pupae can be found (depending on generation) in white cocoons under bark, in cracks in support-stakes, in the folds of leaves or in clusters. They are approximately 0.5 cm long. Initially greenish, they gradually turn dark brown (Photo 4). Photo 2 – Egg Lobesia botrana The average duration in days of the different stages of development is presented in Table 1. Table 1 – Average duration, in days, of the different stages of development of the grapevine moth for the three generations Source: Coscollá (1998) Photo 3 – Larva Lobesia botrana Photo 4 – Pupa Lobesia botrana THE GRAPEVINE MOTH 5 Biology The grapevine moth hibernates as a pupa in vines. In the conditions of the DDR, the moth then progresses through three developmental stages capable of causing damage to grapevine inflorescences/clusters (CARLOS et al., 2007 a). The first adults appear around mid-March, and these appearances are highly staggered (Fig 1). Mortality Diapause Fig. 1 – Biological cycle of Lobesia botrana (adapted from Stockel, 1989) Despite their early flight, the first generation of adults only find suitable clusters for laying eggs on the vines from the second fortnight of April (trace bloom) onward. It is likely that the adults lay eggs on alternative hosts prior to this period. The flight of the adults is crepuscular, and they remain inactive during the day, hidden in leaves or clusters. The first generation of larvae causes damage during the pre-flowering/fruit set period (May), the second generation causes damage when grapes are at the pea-sized stage/veraison (mid-June to mid-July), and the third generation causes damage during ripening (August-September). The adult flights continue until early October (CARLOS et al., 2007 a) (Fig. 2). In the conditions of the DDR, the grapevine moth may have a fourth generation. This generation, however, does not complete its development and is therefore known as a suicide generation. No. of captures / week nests, % clusters attacked adults nests attack Fig. 2 – Flight curve of Lobesia botrana and the frequency of attack of the 1st G (*) and the 2nd/3rd G (¤) in the DDR. ADVID, 2002. ADVID Technical Notes ADVID Technical Notes 6 Damage and Losses The harmfulness of the grapevine moth is closely related to the climatic and microclimatic conditions of the location in which it develops and can vary by region and year. In the DDR, the pest is generally considered highly harmful in the Baixo Corgo, moderately harmful in the Cima Corgo and not very harmful in the Douro Superior. 1st Generation During the month of May, the larvae develop in flower buds, perforating them and joining several flowers with silk threads (Photo 5). The larvae then continue their development inside the resulting glomerule (Photos 6 and 7). These larvae may also form a second glomerule. Several authors have found that grape clusters have a significant capacity for compensation at this stage, with each cluster being able to withstand (depending on the variety) attacks of 1 to 4 glomerules (1 to 2 larvae) or the elimination of 30 flowers per inflorescence with no impact on yield (ROEHRICH & SCHMID, 1979 referred to in TORRES-VILA (1999)). COSCOLLÁ (1980) mention that, in the conditions of the Spanish Levant, the vine is capable of compensating for up to 50% flower loss. Exceptions to this compensatory ability are found in varieties with small clusters and in northern climate conditions that favour early attacks of Botrytis cinerea. In the case of highly compact clusters (e.g., Touriga Franca), the thinning caused by these larvae may be beneficial (Photo 8), as it prevents phenomena such as the expulsion of berries at cluster closure, commonly known as “escadas”, or the bursting of berries during ripening that results in the onset of grey rot or sour rot. Risk assesments by ADVID in the period from 2000 to 2006 suggest a relatively lower economic importance of the first generation in the DDR (CARLOS et al., 2007 b). For this reason, it has become increasingly common not to perform treatments against this generation or to only do so when the attack exceeds the economic injury level (EIL) of 200 nests per 100 clusters sampled. 2 - 06 13 - 06 20 - 06 5 6 7 Photos 5, 6 and 7 – Damage caused by the first generation of the grapevine moth (glomerules) 20 - 07 Photo 8 – Evolution of a cluster (Touriga Franca) attacked by six grapevine moth nests (first generation) 30 - 08 THE GRAPEVINE MOTH 7 2nd Generation In mid-June, eggs are laid on green berries (pea-sized stage/cluster closure), generally in more shaded clusters (CARLOS et al., 2007 a). These 2nd generation larvae establish themselves by perforating the berry peduncle or the point of contact between two berries (Photo 9). The harmfulness of this generation depends on the evolution of climate conditions, the location and the variety. In the event of high temperatures and reduced relative humidity, the attacked berries dry out (Photo 10), and the quantitative production loss is generally not significant. In the event of rainfall, the damage caused by the larva may lead to the early onset of grey rot inside the cluster, particularly among varieties with highly compact clusters on highly vigorous vines. In the DDR, although the frequency of attack can be significant, this frequency does not appear to be reflected in damage levels. This result may be due to the occurrence of climate conditions that are unfavourable for the development of grey rot (CARLOS et al., 2007 b). 9 10 The EIL defined for the 2nd and 3rd generations is 1-10% of the clusters attacked; attacked clusters are defined by having at least one viable egg or one perforation. In the case of well-exposed vines with average vigour, this level of damage may be found in 10% of clusters attacked. Photos 9 and 10 – Damage caused by the 2nd generation of the grapevine moth (perforations) 3rd Generation The third wave of oviposition usually occurs around the first fortnight of August on clusters that are already at the ripening stage (CARLOS et al., 2007 a). The behaviour of larvae in this stage is similar to that of larvae in the 2nd generation. In addition to perforating clusters, however, the also larvae nibble the berries, and several berries damaged by the same larva can often be observed (Photo 11). 11 12 The harmfulness of the grapevine moth is high at this stage because the maturity of the clusters, as well as the climate conditions, may lead to the onset and spread of grey rot (Photos 12, 13 and 14), which significantly lowers the value of the harvest. In the DDR, it is this generation that causes the greatest economic damage, as the climate conditions are more favourable for the development of both the pest and grey rot. Therefore, in the case of vines with a history of attacks, and particularly on varieties with highly compact clusters, such as Touriga Franca, it may be advisable to adopt the lowest economic injury level (1-10%) (CARLOS et al., 2007 b). Photo 11 – Direct damage caused by the 3rd generation of the grapevine moth Photos 12-14 – Attack of grey rot generated by the 3rd generation of the grapevine moth 13 14 ADVID Technical Notes ADVID Technical Notes 8 Risk Assesment Scouting for grapevine moth risk should begin with the placement of a pheromone trap in the vineyard (Photo 15), which is an essential step for determining the periods in which the risk assesment for each generation should be concentrated (they indicate the start and end of the flight period and therefore those of the laying period). The trap must be placed in a vineyard with a history of attacks, at the height of the grape clusters (see information bulletin No. 3 from 2006). In the first generation, wine growers commonly estimate damages at the final flowering stage, during which it is relatively easy to observe the grapevine moth “nests.” This practice leads to the estimation of risk at a significantly advanced stage of larval development, which may impact the effectiveness of insecticide treatment. Observation should thus begin at the trace bloom stage with a search for the glomerules (flower buds spun together) formed by the larva, and the number of glomerules observed per 100 clusters should be recorded (Table 2). Photo 15 – Pheromone trap Table 2 – Proposed risk assesment methodology for Lobesia botrana in the DDR (CARLOS & AGUIAR, 2006) Generation When From trace bloom What to look for Glomerules First signs of the presence of larvae: silk threads, flower buds spun together, excrement, or larvae. 1st Intensification of captures up to 1 week after the peak Viable eggs Perforations (if permitted by the cluster) 2nd Precautions Do not make the estimate based on well-developed nests (from flowering/fruit set - late). EIL 200 nests/clusters Aggravating factors production, presence/absence of beneficials, early incidence of Botrytis or Perform the estimate before cluster closure by carefully observing the cluster interior (point of contact of berries). Check the viability of eggs and the laying intensity/cluster (indicates harmfulness). What is most visible (viable eggs or perforations)? Distinguish them to select the appropriate means of control (ovicide or larvicide). 1-10% clusters attacked (by viable eggs or perforations) Do not treat Aggravating factors climate conditions of the location, variety, presence/absence of beneficials Intensification of captures up to 1 week after the peak 3rd Viable eggs Perforations (if permitted by the cluster) Check the viability of eggs and the laying intensity/cluster (indicates harmfulness). What is most visible (viable eggs or perforations)? Distinguish them to select the appropriate means of control (ovicide or larvicide). Aggravating factors climate conditions of the location, variety, presence/absence of beneficials, early ripening 1-10% clusters attacked (by viable eggs or perforations) THE GRAPEVINE MOTH 9 The intensification of captures on the trap indicates the ideal periods for risk assessment of the 2nd and 3rd generations. These assessments should be geared to the observation of viable eggs on clusters (Photos 16 and 17), as the observation of perforations is difficult, slow and inaccurate due to cluster closure. In the case of the 3rd generation, the perforations are situated within clusters that are at an advanced stage of ripening, which does not allow the observation of the perforations without damage to the clusters. 16 For this reason, it is recommended that the risk for these generations be estimated on the same day that the intensification of captures is observed and that estimations be repeated weekly until a week after the peak of the captures. Prediction models Two moth prediction models are currently used in France: the EVA from the Plant Protection Service, which is distributed through the Service Notices, and the ACTA/ITV, which is included in the program Logiciel Méteo-Pro that is distributed by ACTA. The ACTA/ITV provides timely information on the development of the pest over time based on climate records obtained since the start of the year. This model is an interesting tool for predicting the phenology of the pest, as it indicates the egg-laying period, the hatching of larvae, the development of the larvae and the presence of adults. It does not indicate higher or lower pest pressure, however, which means that management decisions are dependent on the sampling of clusters on the vine. 17 Photo 16 – Comparison of a viable egg (left) and a non-viable egg (right) Photo 17 – Viable eggs from the 3rd generation of the grapevine moth Integrated Pest Management Cultural Precautions Vine-growing practices may indirectly affect moth populations, both through influencing their stages of development and by modifying their behaviour. - Dusting - According to TORRES-VILA (1999), the grapevine moth prefers to lay eggs on undusted clusters rather than on clusters that have been dusted with sulphur, road dust or lime. If there is no substratum, however, the eggs may be laid equally on both clusters. - Pruning and training of the vine - Systems that facilitate air movement around the fruiting organs are recommended. - Leaf Removal - Besides facilitating the penetration of spray into clusters, the direct exposure of the moth eggs to sunlight results in their desiccation. - Harvest Period - The harvesting of clusters with larvae that have not yet abandoned them to pupate may reduce the incidence of the pest. In addition, bringing forward the grape harvest may be recommended if the risk of grey rot is high. Chemical control When deciding whether to perform phytosanitary treatment, the wine grower must take various factors into account. 1 - Insecticide effect / Active ingredient - Visual observation can identify the stage of development of the moth (eggs or perforations) that exists in greater quantities. The wine grower must then choose the active ingredient of the pesticide in accordance with the target of the treatment; products with ovicidal action should be used on eggs, while products with larvicidal action should be used on larvae/perforations (Table 3). ADVID Technical Notes RUNNER methoxyfenozide PRESA “ “ ISONET-L CORAGEN EXPLICIT WG STEWARD CBC (Biosani) DUPONT / BAYER DUPONT DUPONT DOW IND. AFRASA PROBELTE SIPCAM QUIMAGRO AGRISENSE (Biosani) VP SC WG WG SC WP WP WP WP WP WP SC spa EC WG DC DC DC Form. 172 mg / dispenser 200 g/l 30% 30% 480 g/L 18% 18% 6,4% 3,8 % 3,2 % 3,2 % 240 g/L 500 dispensers / ha 15-17,5 ml 12,5 g 12,5 g 10-12 ml 50 g 50 g 50 g 100 g 100 g 100 g 30-40 mL 60 mL 100 mL 240 g/ L 30 - 40 g 25 % 50 mL 50 mL 50 mL Recommended application rate/hl 75 g/L + 30g/L 100 g /L 100 g /L 100 g /L Concent. Mating disruption O+L O-L (+) O-L (+) L L L L L L L L (+) - O L (+) - O O (+) + L O (+) - L O (+) - L O (+) - L O (+) - L Type pheromone contact + ingestion ingestion ingestion contact + ingestion ingestion ingestion ingestion ingestion ingestion ingestion ingestion ingestion + contact contact + ingestion contact + ingestion ingestion + contact ingestion + contact ingestion + contact Mode of action 5-6 months 10 -14 14 14 7 - 14 10 - 12 10 - 12 10 - 12 10 - 12 10 - 12 10 - 12 14-21 21 21 14 21 21 21 Activity in days Is N Xn Xn N Is Is Is Is Is Is Is Is Xi Xn Xn; N Xn; N Xi; N TC 0 28 10 10 14 0 0 0 0 0 0 2 2 14 56 56 56 PHI Before beginning of 1st flight (updated in 2012) Add 20% at borders - at economic threshold Until eggs in black dot stage - “ “ “ “ “ Add 1 kg of sugar / kg formulated product - - - - - - - Comments at economic threshold Eggs in black dot stage (preeclosion) First catch First catch First catch First catch Time of application Legend: PHI – Pre-harvest interval (in days) before harvest | Type: O- ovicide; L- larvicide; A- Adulticide; (+) indicates increased activity | TC – Toxic class : Is- Non toxic; Xi- Irritant; Xn- Noxious; C- corrosive;T- Toxic | Hl- hectolitre (100 l) (E,Z)-7,9- dodecadenyl acetate Mating Disruption clorantraniliprol “ indoxacarb Chemical SPINOSADE BELTHIRUL “ KENOGARD BAYER CROPSCIENCE DOW DOW SYNGENTA SYNGENTA SAPEC AGRO SELECTIS BASF Producer Emulsion, oil in water EW VP EO Emulsion, water in oil EC Vapour Releasing Product Emulsifiable concentrate SL SC DP Dispersible powder Suspension concentrate WG Water Dispersible Granules Soluble concentrate WP Internacional Code Wettable powder Form-Formulation: Legend 10 spinosade TUREX BACTIL X2 “ DIPEL “ Bacillus thurigiensis DIPEL WP MIMIC tebufenozide Biopesticide LUFOX INSEGAR 25 WG fenoxicarb + lufenuron fenoxicarb BINGO SALERO “ CASCADE Trade name “ flufenoxuron Insect growth regulators Active ingredient Table 3- List of recommended products for integrated pest management of European Grapevine Moth ADVID Technical Notes THE GRAPEVINE MOTH 11 ADVID Technical Notes 2 - Persistence of the treatment - The grower should know the number of days during which the product is effective, beginning with the moment of application. If there is still a risk of attack (e.g., intense flight curve) after the product is no longer active, a new risk assesment should be made, and the need for treatment should be reanalysed. 3 - Withdrawal period - The grower should know the period of time between the application of the pesticide and the harvest of the grapes. For the 3rd generation of the moth, particularly for early varieties, great care must be taken to select active substances that do not leave residues on the clusters at the time of the harvest. 4 - Spraying - The main reason for the lack of effectiveness of pesticide treatments against moths is the inappropriate application of the spray to the biological target. Attention must be paid to the flow rate, spray nozzles and their orientation and the recommended working pressure, with respect to the active substance dosage recommended by the product retailers. The effectiveness of the treatment depends on the correct distribution of the product on the treatment target. Treatments against the grapevine moth should be aimed, whenever possible, only at the clusters. The distribution of the spray onto the rest of the vegetation may lead to an under-dosage of the active substance on the clusters. In the particular case of biological control agents used by spraying (Bacillus thurigiensis and spinosad) or of biotechnical control using insect growth regulators or inhibitors (RCI and ICI), the wine grower must take special care to select the active substance according to the pest’s biological cycle (Table 3, Fig. 3). Fig. 3 – Period for the application of active substances acting on Lobesia botrana Mating disruptio ADVID Technical Notes 12 Mating Disruption Mating disruption is method of protection against the grapevine moth that consists of disturbing the encounters between males and females. It is conducted by saturating the atmosphere of the vineyard with the sexual pheromone of Lobesia botrana (E,Z-7.9-dodecadienil acetate) to prevent mating and egg-laying, which prevents the damage caused by the resulting larvae. The synthetic pheromone is distributed by pheromone dispensers (Photo 18). Photo 18 – Pheromone dispenser (ISONET-L) Mating disruption against the grapevine moth has been tested in the Douro by ADVID since 2000 (JORGE, 2000; GASPAR, 2002; COSTA, 2003; DOMINGOS, 2004; CARLOS et al., 2004). The results obtained over this period have not been entirely satisfactory; although in most cases, mating disruption has led to a reduction of larval damage compared with control vineyards, there is almost always a need to perform one or more insecticide treatments on these vineyards to complement mating disruption. However, as the practice offers advantages both in environmental terms (due to the reduction in number of treatments) and in terms of applicator and consumer health, there has been an increasing number of growers using mating disruption, and it is one of the means of protection that should be promoted in integrated pest management (IPM). Biological control Due to the economic importance of the grapevine moth in the DDR, it is important to identity and assess the importance of the pest’s natural enemies, particularly its predators and parasitoids. This knowledge can then be used to develop protection measures that fit into the framework of IPM in viticulture, as has already been performed in other countries. Predators of the grapevine moth The predators of L. botrana include 10 species of spiders and 21 species of insects. Notable predator groups include the Neuroptera, including Chrysoperla carnea (Photo 19 and 20), and the Coleoptera Coccinellidae (Photo 21), Carabidae, Cleridae and Malachiidae (Photo 22), although these latter groups have limited incidence (COSCOLLÁ, 1998). Photo 19 – Green lacewing larva attacking a moth larva Photo 20 – Adult green lacewing Photo 21 – Adult coccinellid (7-spot ladybird) Photo 22 – Adult malachiid beetle ADVID has been performing work in the DDR since 2002 to study the main predator insects active on vines and to identify their periods of activity in the vine growing season. Among the captured insects, the families Chrysopidae (Photos 19 THE GRAPEVINE MOTH 13 and 20) and Malachiidae (Photo 22) were considered to be of greatest interest as potential predators of the grapevine moth. Most of the captures of representatives of these families were reported between June and August/September (CARLOS et al., 2005). Parasitoids of the grapevine moth Approximately 100 types of parasitoids of the grapevine moth are known, including Hymenoptera Ichneumonidae, Braconidae, Pteromalidae and Chalcididae. Their action in reducing populations of the pest is, however, not considered very significant. Hibernating pupae are the exception to this rule, and parasitism rates of approximately 70% have been observed on this developmental stage. Normal pupal parasitism rates are approximately 30-40%, nearly all of which is due to Pteromalidae of the genus Dibrachys (COSCOLLÁ, 1998). Since 2002, ADVID has been identifying the main parasitoids (Photo 23) of the grapevine moth in the DDR and assessing their importance in limiting this pest. Seven species of parasitoids have been identified, the most abundant of which are Elachertus affinis (Masi) (Hym.: Eulophidae) (Photo 24), which represents 32.9% of the total of immersed parasitoids; Brachymeria sp. (Hym.: Chalcididae) (Photo 25), which represents 29.2%; Campoplex capitator (Aubert) (Hym.: Ichneumonidae) (Photo 26), which represents 19.3%, and Dibrachys cavus (Photos 27 and 28), which represents 2.5%. The parasitism rates varied between 2.0 and 50% for the 1st generation and between 6.8 and 36.8% for the 2nd generation (CARLOS et al., 2006). C. capitator was the most abundant species in five of the eight samplings, covering both the 1st and the 2nd generation of the moth. In addition, parasitoids from the families Braconidae, Bethylidae (Hymenoptera) and Tachinidae (Diptera) were also identified, of which only a single specimen was obtained (CARLOS et al., 2006). Photo 23 – Moth larva parasited by hymenoptera larva Photo 24 – Elachertus affinis Photo 25 – Brachymeria sp. Photo 26 – Campoplex capitator Photo 27 – Dibrachys cavus Photo 28 – Dibrachys cavus (inside moth pupa) It is important to further this type of research, to identify the factors that determine the effectiveness of beneficials as natural control agents. According to this point of view and in consideration of both the typical wine farm structure in DDR (vineyards on terraces, comprising small plots that are often separated by embankments) and the Swiss experience (BÖLLER et al., 2004), priority should be given to the identification of potential ecological compensation areas (ECA) as well as the possibility of manipulating them in order to increase the density of beneficials and their effectiveness as agents of natural control of the pest. ADVID Technical Notes ADVID Technical Notes 14 Bibliography BÖLLER, E.F., HÄNI, F. & HANS-MICHAEL, P. (Eds). 2004. Ecological infraestructures: Ideabook on functional biodiversity at the farm level. Temperate zones of Europe. Swiss Centre for Agricultural Extension and Rural Development, Switzerland, 212 p. CARLOS, C.; ALVES, F. & TORRES, L. 2007 a. Ciclo biológico da traça da uva, Lobesia botrana (Den. & Schiff.), na Região Demarcada do Douro. 7º Simpósio de Vitivinicultura do Alentejo. 23 to 25 May 2007, pp 67-74. CARLOS, C.; ALVES, F. & TORRES, L. 2007 b. Importância dos ataques de traça da uva, Lobesia botrana (Den. & Schiff.), na Região Demarcada do Douro.Vititécnica nº 4 (to be published). CARLOS, C. & AGUIAR, A. 2006. Estimativa do risco da traça da uva na Região Demarcada do Douro. Contributo para a sua aferição a nível regional. 1º Encontro sobre Estimativa do Risco. ESACB, 20 April (to be published). CARLOS, C.; COSTA, J.; GASPAR, C; DOMINGOS, J.; ALVES, F. & TORRES, L. 2004. Mating disruption to control the grapevine moth, Lobesia botrana (Den. & Schiff.) in Porto Wine Region vineyards: a three-year study. 6th International Conference on Integrated Fruit Production. Baselga di Piné, Trentino, Italy, 26-30 September 2004, pp 249-253. CARLOS, C.; COSTA, J.R.; TÃO, C.B.; ALVES, F. & TORRES, L.M. 2006 Parasitismo associado à traça da uva, Lobesia botrana (Dennis & Schiffermüller) na Região Demarcada do Douro. Bol. San. Veg. Plagas, 32: 355-362. CARLOS, C., TÃO, C.B., DOMINGOS, J.A., COSTA, J.R., ALVES, F. & TORRES, L.M. 2005. Insectos predadores associados à vinha na Região Demarcada do Douro. VII Encontro Nacional de Protecção Integrada. Escola Superior Agrária de Coimbra, 6-7 December 2005, 388-397. CAVACO, M.; CALOURO, F. & CLÍMACO, P. 2005. Produção Integrada da cultura da vinha. DGPC. Oeiras. 146 pp. COSCOLLÁ, R. 1980. Estudio poblacional, ecológico y económico de la Polilla del racimo de la vid Lobesia botrana Den. & Schiff. en la província de Valencia. Planteamiento de un sistema de lucha dirigida. Tesis Doct. ETSIA, Valencia, 408 pp. COSCOLLÁ R. 1998. Polillas del racimo (Lobesia botrana Den. y Schiff.). In G. Barrios et al. (eds.), Los parásitos de la vid, MAPA-Mundi Prensa, Madrid, 29-42. COSCOLLÁ, R. 2004. Indices de plaga en la polilla del racimo de la vid (Lobesia botrana). 15º Symposium Internacional. Evolución del riesgo de plagas y enfermedades. El muestreo como herramienta esencial en la Protección Integrada. Phytoma España. 164. December 2004, 47-52. COSTA, J.M.R. 2003. Protecção integrada da vinha contra Lobesia botrana (Den. & Schiff.) na Região Demarcada do Douro com recurso à luta biotécnica - método de confusão sexual. Relatório final de estágio. UTAD, Vila Real, 82 pp. DOMINGOS, J.M.A. 2004. Protecção integrada da vinha contra Lobesia botrana (Den. & Schiff) com recurso à luta biotécnica - método de confusão sexual e contribuição para o conhecimento dos insectos predadores associados à cultura da vinha na na Região Demarcada do Douro. Relatório final de estágio. UTAD, Vila Real, 119 pp. GASPAR, C.F. 2002. Protecção integrada da vinha contra Lobesia botrana (Den. & Schiff.) na Região Demarcada do Douro, com recurso à luta biotécnica – método da confusão sexual. Relatório final de estágio. U. Açores, Angra do Heroísmo, 118 pp. JORGE, S.M. 2000. A eudémis da vinha Lobesia botrana (Den. & Schiff.) na Região Demarcada do Douro: curva de voo, estimativa do risco e luta por confusão sexual. Relatório final de estágio. UTAD, Vila Real, 121 pp. TORRES-VILA, L. M. 1999. Un aniversario aciago: dos siglos de historia como plaga de la polilla del racimo de la vid, Lobesia botrana Den. y Schiff. http://www.seea.es/conlupa/lbotrana/lbotrana.htm (consulted on 26-01-2006). STOCKEL, J. 1989. Préconisations Vers de grappe: comment prévoir les risques ?. Connaissance de la vigne et du vin . Hors série, pp 75-80. ADVID is a non-profit association set up in 1982 by companies associated with the production and marketing of wine in the Demarcated Douro Region. Following the change in its statutes in 1997, winegrowing enterprises with different organisational levels, from companies to individual winegrowers, could also join as full or associate members. Its purpose is the study, experimentation, demonstration and dissemination of viticultural techniques suited to the specific characteristics of the Demarcated Douro Region, with a view to the competitiveness and quality of its wines. Recognised since 2009 as the management entity of the Demarcated Douro Region Wine Cluster, its mission is to contribute to a dynamic and consolidated wine production sector in the Douro Region, through a sustainable technology strategy applied to all its stakeholders. The following companies are full members (updated in 2012): Adriano Ramos Pinto - Vinhos, S.A. C.ª Geral da Agricultura das Vinhas do Alto Douro Churchill Graham, Lda. Niepoort (Vinhos), S.A. Quinta do Noval - Vinhos, S.A. Rozès, S.A. Sociedade Vinícola Terras de Valdigem, S.A. Sogevinus Fine Wines, S.A. Sogrape Vinhos, S.A. W. & J. Graham & C.ª, S.A. ADVID • Cluster dos Vinhos da Região Demarcada do Douro Quinta de Sta. Maria, Apartado 137, 5050 - 106 GODIM (PESO DA RÉGUA) Phone: +351 254 312 940 | Fax: +351 254 321 350 E-mail: [email protected] www.advid.pt