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RESPONSE OF THREE CHELONUS (HYMENOPTERA: BRACONIDAE) SPECIES TO KAIROMONES IN SCALES OF SIX LEPIDOPTERA1

Published online by Cambridge University Press:  31 May 2012

A.A. Chiri
Affiliation:
Division of Biological Control, University of California, Riverside, California, USA
E.F. Legner
Affiliation:
Division of Biological Control, University of California, Riverside, California, USA

Abstract

Three species of egg–larval parasites in the genus Chelonus (Hymenoptera: Braconidae) exhibited host-searching behavior when exposed to body scales from 6 species of Lepidoptera representing 3 families. The nonspecific response to scales from several hosts appears to be of adaptive value to Chelonus spp., as it is consistent with the polyphagous habits reported for this genus. The searching response was more widespread and intense in an Ethiopian Chelonus sp. than in 2 other species. It is thought that the broad responsiveness to host scales may detrimentally affect parasite searching ability through excessive loss of searching time, although sensory adaptation to the kairomones might serve to attenuate such effect. Some coevolutionary aspects of this host–parasite chemical interaction are discussed.

Résumé

Trois espèces de parasites d’oeufs–larves appartenant au genre Chelonus (Hymenoptera : Braconidae) ont manifesté le comportement typique de recherche de l’hôte en présence d’écailles provenant d’individus de 6 espèces de lépidoptères représentant 3 familles. La réaction non-spécifique aux écailles de plusieurs hôtes semble adaptative pour ces espèces de Chelonus, puisqu’elle est en accord avec les habitudes polyphages rapportées pour ce genre. La réponse de recherche était plus fréquente et plus intense chez 1 espèce éthiopienne de Chelonus que chez 2 autres espèces. On croit que la sensibilité élevée à la présence d’écaillés d’hôtes pourrait réduire l’efficacité de recherche du parsite dû à la perte de temps passé en recherche inutile, bien que l’adaptation sensorielle aux kairomones pourrait atténuer cet effet. La discussion porte sur certains aspects coévolutifs de cette interation hôte–parasite de nature chimique.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1986

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References

Broodryk, W.W. 1969. The biology of Chelonus (Microchelonus) curvimaculatus Cameron (Hymenoptera: Braconidae). J. Ent. Soc. S. Afr. 32: 169189.Google Scholar
Chiri, A.A., and Legner, E.F.. 1982. Host-searching kairomones alter behavior of Chelonus sp. nr. curvimaculatus, a hymenopterous parasite of the pink bollworm, Pectinophora gossypiella (Saunders). Environ. Ent. 11: 452455.CrossRefGoogle Scholar
Corbet, S.A. 1971. Mandibular gland secretion of larvae of the flour moth, Anagasta kuehniella, contains an epideictic pheromone and elicits oviposition movements in a hymenopterous parasite. Nature 232: 481484.CrossRefGoogle Scholar
Kaissling, K.E. 1977. Control of insect behavior via chemoreceptor organs. pp. 4565in Shorey, H.Y., and McKelvey, J.J. Jr., (Eds.), Chemical control of insect behavior. John Wiley and Sons, New York.Google Scholar
Legner, E.F., and Medved, R.A.. 1979. Influence of parasitic Hymenoptera on the regulation of pink bollworm, Pectinophora gossypiella, on cotton in the lower Colorado Desert. Environ. Ent. 8: 922930.CrossRefGoogle Scholar
Legner, E.F., and Thompson, S.N.. 1977. Effect of the parental host on host selection, reproductive potential, survival, and fecundity of the egg-larval parasitoid, Chelonus sp. nr. curvimaculatus, reared on Pectinophora gossypiella (Saunders) and Phthorimaea operculellu (Zeller). Entomophaga 22: 7584.CrossRefGoogle Scholar
Lewis, W.J., and Jones, R.L.. 1971. Substance that stimulates host-seeking by Microplitis croceipes (Hymenoptera: Braconidae), a parasite of Heliothis species. Ann. ent. Soc. Am. 64: 471473.CrossRefGoogle Scholar
Lewis, W.J. et al. , 1976. The role of kairomones and other behavioral chemicals in host-finding by parasitic insects. Behav. Biol. 16: 267289.CrossRefGoogle ScholarPubMed
McComb, C.W. 1967. A revision of the Chelonus subgenus Microchelonus in North America north of Mexico (Hymenoptera: Braconidae). Bull. Univ. Maryland Agric. Exp. Stn. A-149. 148 pp.Google Scholar
Prokopy, R.J., and Webster, R.P.. 1978. Oviposition-deterring pheromone of Rhagoletis pomonella: A kairomone for its parasitoid Opius lectus. J. Chem. Ecol. 4: 481492.CrossRefGoogle Scholar
Rechav, Y., and Orion, T.. 1975. The development of the immature stages of Chelonus inanitus. Ann. ent. Soc. Am. 68: 457462.CrossRefGoogle Scholar
Vinson, S.B. 1977. Behavioral chemicals in the augmentation of natural enemies. pp. 237279in Ridgway, R.L., and Vinson, S.B. (Eds.), Biological control by augmentation of natural enemies. Plenum Press, New York.CrossRefGoogle Scholar