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Vespula vulgaris (Hymenoptera: Vespidae) gynes use a sex pheromone to attract males

Published online by Cambridge University Press:  21 February 2013

Robert L. Brown ,
Ashraf M. El-Sayed ,
David Maxwell Suckling ,
Lloyd D. Stringer  and
Jacqueline R. Beggs
Robert L. Brown*
Affiliation:
School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand
Ashraf M. El-Sayed
Affiliation:
The New Zealand Institute for Plant & Food Research, Private Bag 4704, Christchurch 8140, New Zealand
David Maxwell Suckling
Affiliation:
The New Zealand Institute for Plant & Food Research, Private Bag 4704, Christchurch 8140, New Zealand
Lloyd D. Stringer
Affiliation:
The New Zealand Institute for Plant & Food Research, Private Bag 4704, Christchurch 8140, New Zealand
Jacqueline R. Beggs
Affiliation:
School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand
*
1Corresponding author (e-mail: [email protected]).
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Abstract

Sex attraction studies were carried out to investigate the mate-finding behaviour of invasive Vespula vulgaris (Linnaeus) (Hymenoptera: Vespidae) wasps. Delta traps were baited with live, caged males, and gynes (virgin queens) of V. vulgaris to determine whether either sex produced a long-range sex attractant. Traps baited with gynes caught 71 males, while the controls and live-male wasp baited traps did not catch gynes. Wind tunnel trials were performed to verify if the signal produced by the gynes was chemical in nature. First, V. vulgaris males were flown to live caged gynes, where more than half of the males tested flew upwind in a zigzagging pattern and made contact with caged gynes. Males were also flown to hexane rinses of gynes and flew upwind in a zigzagging pattern towards the gyne extract, although none made contact with the cotton roll stimulus. The results presented here demonstrate conclusively that V. vulgaris gynes produce a sex pheromone.

Résumé

Des études d'attraction sexuelle ont été réalisées afin d’étudier le comportement de recherche de partenaire chez la guêpe envahissante Vespula vulgaris (Linnaeus) (Hymenoptera: Vespidae). Nous avons appâtés des pièges Delta avec des mâles et des gynes (reines vierges) de V. vulgaris vivants et encagés pour déterminer si l'un ou l'autre des sexes produit une substance d'attraction sexuelle à longue portée. Les pièges appâtés de gynes ont capturé 71 mâles, alors que les pièges témoins et les pièges contenant des guêpes mâles vivantes n'ont attrapé aucune gyne. Des essais en soufflerie aérodynamique ont permis de vérifier si le signal produit par les gynes est de nature chimique. D'abord, nous avons introduit des mâles de V. vulgaris en vol en direction de gynes vivantes encagées: plus de la moitié des mâles se sont dirigés dans le vent en zigzagant et ont fait contact avec les gynes encagées. Nous avons aussi introduit des mâles en vol en direction de rinçages de gynes à l'hexane: les mâles ont volé en zigzagant dans le vent vers l'extrait de gynes, bien qu'aucun n'ait fait contact avec le rouleau de coton servant de stimulus. Nos résultats démontrent de manière décisive que les gynes de V. vulgaris produisent une hormone sexuelle.

Type
Behaviour & Ecology
Information
The Canadian Entomologist , Volume 145 , Issue 4 , August 2013 , pp. 389 - 397
Copyright
Copyright © Entomological Society of Canada 2013 

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References

Baker, T.C.Haynes, K.F. 1987. Manoeuvres used by flying male oriental fruit moths to relocate a sex pheromone plume in an experimentally shifted wind-field. Physiological Entomology, 12: 263–279 . doi:10.1111/j.1365-3032.1987.tb00751.x.CrossRefGoogle Scholar
Barlow, N.D., Moller, H., Beggs, J.R. 1996. A model for the impact of Sphecophaga vesparum vesparum as a biological control agent of the common wasp in New Zealand. Journal of Applied Ecology, 33: 31–44.CrossRefGoogle Scholar
Beggs, J.R., Brockerhoff, E.G., Corley, J.C., Kenis, M., Masciocchi, M., Muller, F., et al. 2011. Ecological effects and management of invasive alien Vespidae. BioControl, 56: 505–526.CrossRefGoogle Scholar
Clare, G., Suckling, D.M., Bradley, S.J., Walker, J.T.S., Shaw, P.W., Daly, J.M., et al. 2000. Pheromone trap colour determines catch of non-target insects. New Zealand Plant Protection, 53: 216–220.CrossRefGoogle Scholar
Dekker, T.Cardé, R.T. 2011. Moment-to-moment flight manoeuvres of the female yellow fever mosquito (Aedes aegypti L.) in response to plumes of carbon dioxide and human skin odour. Journal of Experimental Biology, 214: 3480–3494.CrossRefGoogle ScholarPubMed
El-Sayed, A.M. 2009. Single individual tracking software. New Zealand Institute for Plant and Food Research Ltd, Auckland, New Zealand.Google Scholar
El-Sayed, A.M., Gödde, J., Witzgall, P., Arn, H. 1999. Characterization of pheromone blend for grapevine moth, Lobesia botrana by using flight track recording. Journal of Chemical Ecology, 25: 389–400 . doi:10.1023/a:1020811200054.CrossRefGoogle Scholar
Goodisman, M.A.D., Kovacs, J.L., Hoffman, E.A. 2007. The significance of multiple mating in the social wasp Vespula maculifrons. Evolution, 61: 2260–2267.CrossRefGoogle ScholarPubMed
Greene, A. 1991. Dolichovespula and Vespula. In The social biology of wasps. Edited by K.G. Ross and R.W. Matthews. Comstock Publishing Associates. Ithaca, United States of America and London. Pp. 263–305.Google Scholar
Lacey, E.S.Cardé, R.T. 2011. Activation, orientation and landing of female Culex quinquefasciatus in response to carbon dioxide and odour from human feet: 3-D flight analysis in a wind tunnel. Medical and Veterinary Entomology, 25: 94–103 . doi:10.1111/j.1365-2915.2010.00921.x.CrossRefGoogle Scholar
Landolt, P.J., Jeanne, R.L., Reed, H.C. 1998. Chemical communication in social wasps. In Pheromone communication in social insects: ants, wasps, bees, and termites. Edited by R.K. Vander Meer, M.D. Breed, K.E. Espelie and M.L. Winston. Westview Press, Boulder, Colorado, United States of America. Pp. 216–235.Google Scholar
MacDonald, J.F., Akre, R.D., Hill, W.B. 1974. Comparative biology and behaviour of Vespula atropilosa and V. pensylvanica (Hymenoptera: Vespidae). Melanderii, 18: 1–66.Google Scholar
MacKenzie, J.K., Landolt, P.J., Zack, R.S. 2008. Sex attraction in Polistes dominulus demonstrated using olfactometers and morphological source extracts. Journal of the Entomological Society of British Columbia, 105: 35–43.Google Scholar
Mhatre, N.Balakrishnan, R. 2007. Phonotactic walking paths of field crickets in closed-loop conditions and their simulation using a stochastic model. Journal of Experimental Biology, 210: 3661–3676 . doi:10.1242/jeb.003764.CrossRefGoogle ScholarPubMed
Moller, H., Beggs, J.R., Tilley, J.A.V., Toft, R.J., Wilson, N.J., Alspach, P.A. 1990. Ecology and control of the wasp populations in New Zealand. Contract Report to the Department of Conservation, Wellington, New Zealand.Google Scholar
Ono, M.Sasaki, M. 1987. Sex pheromones and their cross-activities in six Japanese sympatric species of the genus Vespa. Insectes Sociaux, 34: 252–260.CrossRefGoogle Scholar
Post, D.C. 1980. Observations on male behavior of the eastern yellowjacket (Hymenoptera: Vespidae). Entomological News, 91: 113–116.Google Scholar
Post, D.C.Jeanne, R.L. 1983. Source of a sex pheromone in the social wasp Polistes fuscatus (Hymenoptera: Vespidae). Journal of Chemical Ecology, 9: 259–266.CrossRefGoogle Scholar
Post, D.C.Jeanne, R.L. 1984. Venom as an interspecific sex pheromone, and species recognition by a cuticular pheromone in paper wasps (Polistes, Hymenoptera: Vespidae). Physiological Entomology, 9: 65–75.CrossRefGoogle Scholar
Post, D.C.Jeanne, R.L. 1985. Sex pheromone in Polistes fuscatus (Hymenoptera: Vespidae): effect of age, caste and mating. Insectes Sociaux, 32: 70–77.CrossRefGoogle Scholar
R Core Team 2012. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria.Google Scholar
Reed, H.C.Landolt, P.J. 1990a. Queens of the southern yellowjacket, Vespula squamosa, produce sex attractant (Hymenoptera: Vespidae). Florida Entomologist, 73: 687–689.CrossRefGoogle Scholar
Reed, H.C.Landolt, P.J. 1990b. Sex attraction in paper wasp, Polistes exclamans Viereck (Hymenoptera, Vespidae), in a wind-tunnel. Journal of Chemical Ecology, 16: 1277–1287.CrossRefGoogle Scholar
Reed, H.C.Landolt, P.J. 1991. Swarming of paper wasp (Hymenoptera, Vespidae) sexuals at towers in Florida. Annals of the Entomological Society of America, 84: 628–635.CrossRefGoogle Scholar
Ross, K.G. 1983. Laboratory studies of the mating biology of the eastern yellowjacket, Vespula maculifrons (Hymenoptera: Vespidae). Journal of the Kansas Entomological Society, 56: 523–537.Google Scholar
Rutkowski, A., Quinn, R., Willis, M. 2009. Three-dimensional characterization of the wind-borne pheromone tracking behavior of male hawkmoths, Manduca sexta. Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology, 195: 39–54 . doi:10.1007/s00359-008-0380-9.CrossRefGoogle ScholarPubMed
Spiewok, S., Schmolz, E., Ruther, J. 2006. Mating system of the European hornet Vespa crabro: male seeking strategies and evidence for the involvement of a sex pheromone. Journal of Chemical Ecology, 32: 2777–2788 . doi:10.1007/s10886-006-9162-4.CrossRefGoogle ScholarPubMed
Spradbery, J.P. 1973. Wasps: an account of the biology and natural history of social and solitary wasps. University of Washington Press, Seattle, United States of America.Google Scholar
Thomas, C.R. 1960. The European wasp (Vespula germanica Fab.) in New Zealand. New Zealand Department of Scientific and Industrial Research Information Series, 27: 1–74.Google Scholar
Willis, M.A.Baker, T.C. 1994. Behaviour of flying oriental fruit moth males during approach to sex pheromone sources. Physiological Entomology, 19: 61–69 . doi:10.1111/j.1365-3032.1994.tb01075.x.CrossRefGoogle Scholar