Hostname: page-component-8448b6f56d-gtxcr Total loading time: 0 Render date: 2024-04-24T18:43:01.176Z Has data issue: false hasContentIssue false

Developing techniques for monitoring forest tent caterpillar populations using synthetic pheromones

Published online by Cambridge University Press:  02 April 2012

B. Christian Schmidt*
Affiliation:
Department of Biological Sciences, CW 405, Biological Science Building, University of Alberta, Edmonton, Alberta, Canada T6G 2E9
Jens Roland
Affiliation:
Department of Biological Sciences, CW 405, Biological Science Building, University of Alberta, Edmonton, Alberta, Canada T6G 2E9
*
1Corresponding author (e-mail: bjorn@ualberta.ca).

Abstract

To effectively monitor forest tent caterpillar, Malacosoma disstria Hübner (Lepidoptera: Lasiocampidae), populations using sex pheromone baited traps, we field-tested pheromone dispenser (lure) type, lure age, and trap design using (Z,E)-5,7-dodecadienal:(Z,Z)-5,7-dodecadienal (100:1). Rubber septa lures, polyurethane lures, and two trap types [sticky-type pheromone traps (Wing Trap I) and bucket-type pheromone traps (Universal Moth trap)] were evaluated. Traps baited with polyurethane lures produced higher trap catches and lower zero-catch frequencies than did rubber septa traps. There was no detectable difference in trap catch among polyurethane lures aged 0–28 days. Wing traps reached a functional saturation point in outbreak M. disstria populations and caught fewer moths than Universal traps in nonoutbreak populations. A nonsaturating trap such as the Universal trap in conjunction with the polyurethane lure should be effective for monitoring M. disstria populations.

Résumé

Pour suivre efficacement des populations de livrées des forêts, Malacosoma disstria Hübner (Lepidoptera: Lasiocampidae), au moyen de pièges garnis de phéromone, nous avons testé sur le terrain le type de distributeur (leurre), l'âge du leurre et le design du piège avec du (Z,E)-5,7-dodécadienal: (Z,Z)-5,7-dodécadienal (100: 1). Des leurres à septums de caoutchouc, des leurres de polyuréthane et deux types de pièges [(pièges collants à phéromones (pièges à ailettes de type I) et pièges phéromones de type seau (Universal Moth trap)] ont été évalués. Les pièges garnis de leurres de polyuréthane ont donné un meilleur rendement et produit moins de captures à fréquence zéro que les pièges à leurres à septums de caoutchouc. Il n'y avait pas de différence perceptible entre les taux de capture des divers pièges de polyuréthane en opération depuis 0–28 jours. Les pièges à ailettes ont atteint un point de saturation fonctionnel au moment des invasions des populations de livrées et capturé moins de livrées que des pièges Universal en dehors des périodes de foisonnement. La combinaison d'un piège non saturable comme le piège Universal et d'un leurre de polyuréthane semble constituer une technique bien appropriée à l'étude des populations de M. disstria.

[Traduit par la Rédaction]

Type
Articles
Copyright
Copyright © Entomological Society of Canada 2003

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Angerilli, N., McLean, J.A. 1984. Wind tunnel and field observations of western spruce budworm responses to pheromone-baited traps. Journal of the Entomological Society of British Columbia 81: 10–6Google Scholar
Bryson, C. 1989. Aspen: Alberta's newest Cinderella Crop. Agriculture and Forestry Bulletin. 1989(3): 11–7Google Scholar
Butler, L.I., McDonough, L.M. 1981. Insect sex pheromones: evaporation rates of alcohols and acetates from natural rubber septa. Journal of Chemical Ecology 7: 627–33CrossRefGoogle ScholarPubMed
Chisholm, M.D., Underhill, E.W., Steck, W., Slessor, K.N., Grant, G.G. 1980. (Z)-5,(E)-7dodecadienal and (Z)5,(E)-7-dodecadien-1-ol, sex pheromone components of the forest tent caterpillar, Malacosoma disstria. Environmental Entomology 9: 278–82CrossRefGoogle Scholar
Chisholm, M.D., Palaniswamy, P., Underhill, E.W. 1982. Orientation disruption of male forest tent caterpillar (Malacosoma disstria Hbn.) (Lepidoptera: Lasiocampidae), by air permeation with sex pheromone components. Environmental Entomology 11: 1248–50CrossRefGoogle Scholar
Churchill, G.B., John, H.H., Duncan, D.P., Hodson, A.C. 1964. Long-term effects of defoliation of aspen by the forest tent caterpillar. Ecology 45: 630–3CrossRefGoogle Scholar
Cooke, B.J. 2001. Interactions between climate, trembling aspen, and outbreaks of forest tent caterpillar in Alberta. PhD thesis, University of Alberta, EdmontonGoogle Scholar
Daterman, G.E. 1982. Monitoring insects with pheromones: trapping objectives and bait formulations. pp 195212in Kydonieus, A.F., Beroza, F. (Eds), Insect suppression with controlled release pheromone systems. Boca Raton, Florida: CRC Press IncGoogle Scholar
Elkinton, J.S., Childs, D. 1983. Efficiency of two gypsy moth (Lepidoptera: Lymantriidae) pheromone baited traps. Environmental Entomology 12: 1519–25CrossRefGoogle Scholar
Ferguson, D.C. 1978. Noctuoidea, Lymantriidae. In Dominick, R.B. et al. (Eds), The moths of America north of Mexico, fascicle 27.3. London: EW Classey LtdGoogle Scholar
Heath, R.R., Teal, P.E.A., Tumlinson, J.H., Mengelkoch, L.J. 1986. Prediction of release ratios of multicomponent pheromones from rubber septa. Journal of Chemical Ecology 12: 2133–43CrossRefGoogle ScholarPubMed
Hendricks, D.E., Calcote, V.R. 1991. Performance of two designs and color combinations of traps baited with sex pheromone for monitoring hickory shuckworm moths in pecan orchards. Southwestern Entomologist 16: 237–42Google Scholar
Lewis, T., Macauley, E.D.M. 1976. Design and evaluation of sex-attractant traps for pea moth, Cydia nigricana (Steph.) and the effect of plume shape on catches. Ecological Entomology 1: 175–87CrossRefGoogle Scholar
Lindgren, B.S., Sweeney, J.D., McLean, J.A. 1984. Comparative evaluation of traps for monitoring the Douglasfir tussock moth (Lepidoptera: Lymantriidae). Journal of the Entomological Society of British Columbia 81: 39Google Scholar
Lopez, J.D. Jr 1998. Evaluation of some commercially available trap designs and sex pheromone lures for Spodoptera exigua (Lepidoptera: Noctuidae). Journal of Economic Entomology 91: 517–21CrossRefGoogle Scholar
McDonough, L.M., Aller, L.D., Knight, A.L. 1992. Performance characteristics of a commercial controlled-release dispenser of sex pheromone for control of codling moth (Cydia pomonella) by mating disruption. Journal of Chemical Ecology 18: 2177–89CrossRefGoogle ScholarPubMed
Meidinger, D., Pojar, J. 1991. Ecosystems of British Columbia. Victoria: British Columbia Ministry of Forests Research BranchGoogle Scholar
Myers, J.H., Kukan, B. 1995. Changes in the fecundity of forest tent caterpillars: a correlated character of disease resistance or sublethal effect of disease? Oecologia 103: 475–80CrossRefGoogle ScholarPubMed
Otvos, I.S., Payne, L., Kilvert, V., Conder, N. 1998. An annotated bibliography of the forest tent caterpillar, Malacosoma disstria. Canadian Forestry Service Pacific Forest Research Centre Report BC–X–380Google Scholar
Palaniswamy, P., Chisholm, M.D., Underhill, E.W., Reed, D.W., Peesker, S.J. 1983. Disruption of forest tent caterpillar (Lepidoptera: Lasiocampidae) orientation to baited traps in aspen groves by air permeation with (5Z,7E)-5,7-dodecadienal. Journal of Economic Entomology 76: 1159–63CrossRefGoogle Scholar
Parry, D., Spence, J.R., Volney, W.J.A. 1997. Responses of natural enemies to experimentally increased populations of the forest tent caterpillar, Malacosoma disstria. Ecological Entomology 22: 97108CrossRefGoogle Scholar
Pendrel, B.A. 1991. Insect and disease caused losses of wood volume in the forests of the Maritime Provinces, 1982–1987. Canadian Forestry Service Maritime Forest Research Centre Report M–X–180EGoogle Scholar
Peterson, E.B., Peterson, N.M. 1992. Ecology, management, and use of aspen and balsam poplar in the prairie provinces. Canadian Forestry Service Northern Forestry Research Centre Special Report 1Google Scholar
Roland, J., Taylor, P.D. 1997. Insect parasitoid species respond to forest structure at different spatial scales. Nature (London) 381: 120CrossRefGoogle Scholar
Sanders, C.J. 1986. Accumulated dead insects and killing agents reduce catches of spruce budworm (Lepidoptera: Tortricidae) male moths in sex pheromone traps. Journal of Economic Entomology 79: 1351–3CrossRefGoogle Scholar
Schmidt, B.C., Roland, J., Wakarchuk, D. 2003. Evaluation of synthetic pheromones for monitoring forest tent caterpillar (Lepidoptera: Lasiocampidae) populations. Environmental Entomology. In pressCrossRefGoogle Scholar
Shepherd, R.F., Brown, C.E. 1971. Sequential egg-band sampling and probability methods of predicting defoliation by Malacosoma disstria (Lasiocampidae: Lepidoptera). The Canadian Entomologist 103: 1371–9CrossRefGoogle Scholar
Shepherd, R.F., Gray, T.G., Chorney, R.J., Daterman, G.E. 1985. Pest management of Douglas-fir Tussock moth, Orgyia pseudotsugata (Lepidoptera: Lymantriidae): monitoring endemic populations with pheromone traps to detect incipient outbreaks. The Canadian Entomologist 117: 839–48CrossRefGoogle Scholar
Struble, D.L. 1970. A sex pheromone in the forest tent caterpillar. Journal of Economic Entomology 63: 295–6CrossRefGoogle Scholar
Vincent, C., Roy, M., Bouchier, P. 1993. Concomitant monitoring of several lepidopteran species in Quebec apple orchards with pheromone traps. Revue d'Entomolgie du Quebec 36: 1525Google Scholar
Zar, J.H. 1999. Biostatistical analysis. 4th ed. Upper Saddle River, New Jersey: Prentice-Hall IncGoogle Scholar