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FACTORS AFFECTING SPRUCE BUDWORM (CHORISTONEURA FUMIFERANA) (CLEM.) MATING AND MATING DISRUPTION WITH PHEROMONE IN THE LABORATORY

Published online by Cambridge University Press:  31 May 2012

B.M. Ponder
Affiliation:
Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 6E1
L.R. Kipp
Affiliation:
Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 6E1
C. Bergh
Affiliation:
Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 6E1
G.C. Lonergan
Affiliation:
Department of Chemistry, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 6E1
W.D. Seabrook
Affiliation:
Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 6E1
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Abstract

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Factors influencing spruce budworm (Choristoneura fumiferana) mating and mating suppression in an enclosed environment in the laboratory were investigated to develop a quantitative assay suited to statistical analysis. Mating in the absence of the two major components of spruce budworm sex pheromone (control) was not affected by changes in moth population density nor by increasing the experimental duration from 20 to 44 h. The proportions mated increased with an increase in the male:female ratio to 1.5:1 and when the experimental duration was prolonged to 68 h. Using a population density, sex ratio combination of 15:10 (male:female) the proportions of mated females decreased with increasing source concentrations of the two major spruce budworm sex pheromone components (95:5 E/Z-11–14-tetradecenal). This effect was diminished with increases in the population density and with extended test duration. Mating in the presence of pheromone remained lower than controls over all durations tested.

Résumé

On a fait une enquête sur les facteurs qui influencent l’accouplement et l’élimination de l’accouplement de la toudeuse de l’épinette (Choristoneura fumiferana) dans un milieu clos en laboratoire pour développer un essai qualitatif approprié aux analyses statistiques. L’accouplement en absence des deux principaux composants du pheromone sexuel (contrôle) de la toudeuse de l’épinette n’a pas été affecté par les changements dans la densité de la population du papillon de nuit, ni par l’augmentation de la durée de l’expérience de 20 en 44 h. La proportion des accouplés augmente avec une augmentation dans le ratio mâle : femelle à 1.5 : 1 et quand la durée de l’expérience a été prolongée à 68 h. Utilisant une combinaison densité de population, ratio sexuel de 15 : 10 (mâle : femelle) les proportions de femelles accouplées diminuent avec une augmentation des concentrations de source de deux principaux composants du phéromone sexuel de la toudeuse de l’épinette (95 : 5 E/Z-11–14-tétradécenal). Cet effet était diminué avec les augmentations dans la densité de population et avec une prolongation de la durées du test. L’accouplement en présence du pheromone restait inférieur aux contrôles par rapport à toutes les durée des tests.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1986

References

Abbott, W.S. 1925. A method for computing the effectiveness of an insecticide. J. econ. Ent. 18: 265267.CrossRefGoogle Scholar
Baker, T.C., Cardé, R.T., and Miller, J.R.. 1980. Oriental fruit moth pheromone component emission rates measured after collection by glass-surface adsorption. J. Chem. Ecol. 6: 749758.CrossRefGoogle Scholar
Bartell, R.J. 1982. Mechanisms of communication disruption by pheromone in the control of Lepidoptera: a review. Physiol. Ent. 7: 353364.Google Scholar
Bergh, J.C., and Seabrook, W.D.. 1986. A simple technique for indexing the mating status of male spruce budworm, Choristoneura fumiferana (Lepidoptera: Tortricidae). Can. Ent. 118: 3741.CrossRefGoogle Scholar
Carles, J.P., Fleurat-Lessard, F., and Roehrich, R.. 1979. Un appareil pour les essais biologiques de comportement de lépidoptères exposés à des doses élevées d'attractif sexuel. Biol. Behav. 4: 205217.Google Scholar
Charmillot, P.J., Rosset, S., and Rhyn, D.. 1976. Comportement sexuel du carpocapse (Laspeyresia pomonella L.): influence de attractif synthétique. Mitt. Schweiz. Entomol. Ges. 49: 143154.Google Scholar
Daniel, W.W. 1978. Applied nonparametric statistics. Houghton Mifflin Co., Boston.Google Scholar
Fluri, P., Mani, E., Wildbolz, T., and Arn, H.. 1974. Untersuchungen über das Paarungsverhalten des Apfel-wicklers (Laspeyresia pomonella L.) und über Einfluss von Kunstlichem Sexuallockstoff auf die Koplationshaüfigheit. Mitt. Schweiz. ent. Ges. 47: 253.Google Scholar
Grisdale, D. 1973. Large volume preparation and processing of a synthetic diet for insect rearing. Can. Ent. 105: 15531557.CrossRefGoogle Scholar
Hagstrum, D.W., and Davis, L.R. Jr., 1982. Mate-seeking behaviour and reduced mating by Ephestia cautella (Walker) in a sex pheromone-permeated atmosphere. J. Chem. Ecol. 8: 507515.CrossRefGoogle Scholar
Hirai, Y., and Mitchell, E.R.. 1982. Sex pheromone of fall armyworm: laboratory evaluation of male response and inhibition of mating by pheromone components. J. Chem. Ecol. 8: 267273.CrossRefGoogle ScholarPubMed
Lonergan, G.C. 1986. Metabolism of pheromone components and analogues by cuticular enzymes of Choristoneura fumiferana. J. Chem. Ecol. 12: 483496.CrossRefGoogle Scholar
McLaughlin, J.R., and Hagstrum, D.W.. 1976. Effects of a dark environment and air permeation with synthetic sex pheromone on mating in the Almond moth. Environ. Ent. 5: 10571058.CrossRefGoogle Scholar
McMorran, A. 1965. A synthetic diet for the spruce budworm, Choristoneura fumiferana (Clem.) (Lepidoptera: Tortricidae). Can. Ent. 97: 5862.CrossRefGoogle Scholar
Morse, D., and Meighen, E.. 1984. Detection of pheromone biosynthetic and degradative enzymes in vitro. J. Biol. Chem. 259: 475480.CrossRefGoogle ScholarPubMed
Outram, I. 1971. Aspects of mating in the spruce budworm, Choristoneura fumiferana (Lepidoptera: Tortricidae). Can. Ent. 103: 11211128.CrossRefGoogle Scholar
Palaniswamy, P., Ross, R.J., Seabrook, W.D., Lonergan, G.C., Weisner, C.J., Tan, S.H., and Silk, P.J.. 1982. Mating suppression of caged spruce budworm (Lepidoptera: Tortricidae) moths in different pheromone atmospheres and high population densities. J. econ. Ent. 75: 989993.CrossRefGoogle Scholar
Ramaswamy, S.B., and Cardé, R.T.. 1984. Rate of release of spruce budworm pheromone from virgin females and synthetic lures. J. Chem. Ecol. 10: 17.CrossRefGoogle ScholarPubMed
Roehrich, R., and Carles, J.P.. 1977. Perturbations dans la reproduction de Lobesia botrana Schiff (Lepidoptera: Tortricidae) induites par la présence de la phéromone sexuelle de synthèse. C.R. Acad. Sci Paris 285: 237239.Google Scholar
Roelofs, W.L., and Comeau, A.. 1971. Sex pheromone perception: electroantennogram responses of the red-banded leaf roller moth. J. Insect Physiol. 17: 19691982.CrossRefGoogle ScholarPubMed
Ross, R.J., Lonergan, G.C., Valenta, Z., Palaniswamy, P., Seabrook, W.D., Darvesh, S., and Oda, T.. 1982. Electroantennograms and trapping with spruce budworm (Lepidoptera: Tortricidae) sex pheromone analogues. Environ. Ent. 11: 12851289.CrossRefGoogle Scholar
Ross, R.J., Palaniswamy, P., and Seabrook, W.D.. 1979. Electroantennograms from spruce budworm moths (Choristoneura fumiferana) (Lepidoptera: Tortricidae) of different ages and for various pheromone concentrations. Can. Ent. 111: 807816.CrossRefGoogle Scholar
Rothschild, G.H.L. 1981. Mating disruption of lepidopterous pests: current status and future prospects. pp. 207228.in Mitchell, E.R. (Ed.), Management of Insect Pests with Semiochemicals. Plenum Press, New York and London.CrossRefGoogle Scholar
Sanders, C.J. 1971. Laboratory bioassay of the sex pheromone of the female eastern spruce budworm, Choristoneura fumiferana (Lepidoptera: Tortricidae). Can. Ent. 103: 631637.CrossRefGoogle Scholar
Sanders, C.J. 1979. Mate location and mating in eastern spruce budworm. Bimon. Res. notes 35: 23.Google Scholar
Schmidt, J.O., and Seabrook, W.D.. 1979. Mating of caged spruce budworm moths in pheromone environments. J. econ. Ent. 72: 509511.CrossRefGoogle Scholar
Schmidt, J.O., Seabrook, W.D., Lonergan, G., Oda, T., Darvesh, S., and Valenta, Z.. 1980. Effects of pheromone, pheromone components, and pheromone analogues on mating of spruce budworm (Lepidoptera: Tortricidae). Can. Ent. 112: 605608.CrossRefGoogle Scholar
Shorey, H.H., Gaston, L.K., and Saario, C.A.. 1967. Sex pheromones of noctuid moths. XIV. Feasibility of behavioural control by disrupting pheromone communication in cabbage loopers. J. econ. Ent. 60: 15411545.CrossRefGoogle Scholar
Silk, P.J., and Kuenen, L.P.S.. 1986. Spruce budworm Choristoneura fumiferana chemistry and behavioural responses to pheromone components and analogs. J. Chem. Ecol. 12: 367383.CrossRefGoogle ScholarPubMed
Sokal, R.R., and Rohlf, J.F.. 1981. Biometry, 2nd ed. W.H. Freeman and Co., San Fransisco. 859 pp.Google Scholar
Smith, R.L., Flint, H.M., and Forey, D.E.. 1978. Air permeation with gossyplure: feasibility studies on chemical confusion for control of the pink bollworm. J. econ. Ent. 71: 257264.CrossRefGoogle Scholar
Sower, L.L., Turner, W.K., and Fish, J.C.. 1975. Population-density-dependent mating frequency among Plodia interpunctella (Lepidoptera: Phycitidae) in the presence of synthetic sex pheromone with behavioural observations. J. Chem. Ecol. 1: 335342.CrossRefGoogle Scholar
Vick, K.W., Coffelt, J.A., and Sullivan, M.A.. 1978. Disruption of pheromone communication in the angoumois grain moth with synthetic female sex pheromone. Environ. Ent. 7: 528531.CrossRefGoogle Scholar
Zar, J.H. 1984. Biostatistical analysis. Prentice-Hall, Englewood Cliffs, NJ. 718 pp.Google Scholar