Practical Winery
65 Mitchell Blvd, San Rafael, CA 94903
phone: 415-453-9700 ext 102
1 · 2 · 3 · 4 · 5
Biological control — Parasitic wasps can parasitize the eggs of L. botrana. Trichogamma species are known egg-parasites of many Lepidoptera species, and can be a good source of biological control of European grapevine moth. In the fall of 2009, egg parasitism was observed in Oakville in vineyards with L. botrana damage.
Studies are needed to determine how early in the season Trichogamma species begin to parasitize L. botrana eggs, if other species of native parasites attack the larval or pupal stages, and the impact these parasitesmay have onmoth populations. In France, Italy, and Spain, the highest parasitism is reported on the diapausing pupa stage. In Europe, green lacewings are among the main predators in summer and spiders are important predators of larvae and diapausing pupae.
Mating disruption — Female moths emit a plume of sex pheromone that males followupwind to find females and mate. Scores of dispensers loaded with synthetic pheromone and deployed throughout a vineyard cause the air to become saturated with the pheromone, such thatmalemoths are unable to locate females, preventing or delaying mating. In the absence of mating or if the female is too old when mated, viable eggs are not laid and no larvae are produced to damage grape clusters.
Mating disruption has proven most effective when European grapevine moth populations are lowandwhen synthetic pheromone is applied to large areas of over 10 acres or area-wide. If moth populations are high, supplemental insecticide applications may be needed.
At press time, no pheromone dispenser product has been registered for use in the U.S., though at least one manufacturer is seeking registration with the U.S. Environmental Protection Agency. The pheromone product undergoing registration is a handapplied dispenser that is attached to trellis wires or canes.
Mating disruption dispensers must be placed in the vineyard at the beginning of the male moth flight, as indicated by the first catch in pheromone traps. Follow manufacturer recommendations for the application rate of dispensers per acre.
Once mating disruption dispensers are registered for use and deployed in vineyards, the pheromone emitted by the dispensers coupled with the lure pheromone in the traps will cause very few moths to be caught in the traps (trap shutdown). Regardless, traps are useful to monitor a vineyard under mating disruption.
Place pheromone traps along the edges and in the center of the block. The edge traps give an indication of movement of male moths into the vineyard. The center traps should catch very few or nomoths. If the center traps are catching males, then mating is not being disrupted and supplemental insecticide applications may be needed. Monitor eggs at peak trap catch and periodically sample grape clusters for the presence of worms or damage.
Sanitation of equipment will be critical to minimize movement of this insect from infested vineyards to non-infested vineyards and to avoid the spread to other regions of California. Equipment should be washed prior to leaving an infested property, preferablywith a highpressure sprayer and hot water. This is especially important for all machinery and containers that come in contact with fruit during harvest.
Larvae can hide in tight places, and fully formed larvae may form a cocoon and pupate in any protected place. When hiring an outside company to harvest fruit, verify that the contractor follows good sanitation practices. Loads will need to be covered during shipment to the winery, and winery waste that does not undergo fermentation will need to be composted.
Briere, J. F., P. Pracros. 1998. “Comparison of temperature- dependent growth models with the development of Lobesia botrana (Lepidoptera: Tortricidae).” Environ. Entomol. 27 (1): 94–101.
CEI 1974. “Lobesia botrana (Schiff).Distributionmaps of pests, Series A, Map No. 70.” Commonwealth Institute of Entomology, Commonwealth Agricultural Bureau. London,
Coscolla, R. 1998. “Polillas del racimo (Lobesia botrana Den. Y Shiff).” In Los parasitos de la vid, estrategias de proteccion razonada. Madrid, Spain. pp. 29–42.
Del Tío, R., J.L. Martínez, R. Ocete, M.E. Ocete. 2001. “Study of the relationship between sex pheromone trap catches of Lobesia botrana (Den. & Schiff.) (Lep., Tortricidae) and the accumulation of degree-days in Sherry vineyards (SW of Spain).” J. Appl. Entomol. 125: 9–14
Deseö, K.V., F.M.A. Brunelli, A. Bertaccini. 1981. “Observations on the biology and diseases of Lobesia botrana Den. and Schiff. (Lepidoptera: Tortricidae) in central-north Italy.” Acta Phytopathologia Acad. Sci. Hungarica 16: 405–431.
Gabel, B., V. Mocko. 1986. “A functional simulation of European vine moth Lobesia botrana Den. Et Schiff. (Lep., Torticidae) population development.” J. Appl. Entomol. 101: 121–127.
Louis, F., A. Schmidt-Tiedemann, K. J. Schirra. 2002. “Control of Sparganothis pilleriana Schiff. and Lobesia botrana Den. & Schiff. in German vineyards using sex pheromone-mediated mating disruption.” Bull. IOBC/WPRS 25: 1–9.
Maher, N., D. Thiéry. 2006. “Daphne gnidium, a possible native host plant of the European grapevine moth Lobesia botrana, stimulates its oviposition. Is a host shift relevant?” Chemoecol. 16: 135–144.
Masante-Roca, I., S. Anton, L. Delbac, M.C. Dufour, C. Gadenne. 2007. “Attraction of the grapevine moth to host and non-host plant parts in the wind tunnel: effects of plant phenology, sex, and mating status.” Entomol. Exp. Appl. 122: 239–245.
Milonas. P.G., M. Savopoulou-Soultani, D.G. Stavridis. 2001. “Day-degree models for predicting the generation time and flight activity of local populations of Lobesia botrana (Den. and Schiff.) (Lepidoptera: Tortricidae) in Greece.” J Appl. Entomol. 125 (9-10): 515–518.
Mondy, N., P. Pracros, M. Fermaud, M.F. Corio- Costet. 1998. “Olfactory and gustatory behaviour by larvae of Lobesia botrana in response to Botrytis cinerea.Entomol. Exp. Appl. 88 (1): 1–7.
Rapagnani, M.R., V. Caffarelli, M. Barlattani. 1989. “Oviposition at various constant and variable temperatures by Lobesia botrana Den. and Schiff. (Lepidoptera: Tortricidae).” Boll. Lab. Entomol. Agraria Filippo Silvestri 46: 45–58.
Roditakis, N.E., M.G. Karandinos. 2001. “Effects of photoperiod and temperature on pupal diapause induction of grape berry moth Lobesia botrana.” Physiol. Entomol. 26: 329–340.
Savopoulou-Soultani,M.,M.E. Tzanakakis. 1990. “Head-capsule width of Lobesia botrana (Lepidoptera: Tortricidae) larvae reared on three different diets.” Ann. Entomol. Soc. Am. 83 (3): 555–558.
Thiéry, D. 2008. “Les Tordeuses nuisibles à la vigne.” In Les ravageurs de la vigne. Féret, Bordeaux. pp. 15.
Torres-Vila, L.M., M.C. Rodriguez-Molina, J. Stockel. 2002. “Delayed mating reduces reproductive output of female European grapevine moth, Lobesia botrana (Lepidoptera: Tortricidae).” Bull. Entomol. Res. 92 (3): 241–249.
Tzanakakis, M.E., M. Savopoulou-Soultani, C. S. Oustapassidis, S.C. Verras, H. Hatziemmanuel. 1988. “Induction of dormancy in Lobesia botrana by long day and high temperature conditions.” Entomol. Hellenica 6: 7–10.
Zangheri, S., G. Briolini, P. Cravedi, C. Duso, F. Molinari, E. Pasqualini. 1992. “Lobesia botrana (Denis & Schiffermüller).” In Lepidotteri dei fruttiferi e della vite. Milan, Italy. pp. 85–88.