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Detection of host habitat by parasitoids using cues associated with mycangial fungi of the mountain pine beetle, Dendroctonus ponderosae

Published online by Cambridge University Press:  02 April 2012

A.S. Adams*
Affiliation:
Department of Ecosystem and Conservation Sciences, College of Forestry and Conservation, University of Montana, Montana 59812, United States of America
D.L. Six
Affiliation:
Department of Ecosystem and Conservation Sciences, College of Forestry and Conservation, University of Montana, Montana 59812, United States of America
*
1 Corresponding author (e-mail: [email protected]).

Abstract

Cues used by parasitoids to detect habitat of the mountain pine beetle, Dendroctonus ponderosae Hopkins (Coleoptera: Curculionidae), were investigated by observing parasitoid attraction to logs infested with D. ponderosae, logs inoculated with one or both of the symbiotic fungi of D. ponderosae (Grosmannia clavigera (Rob.-Jeffr. & R.W. Davidson) Zipfel, Z.W. de Beer & M.J. Wingf. (Ophiostomataceae) and Ophiostoma montium (Rumbold) Arx (Ophiostomataceae)), logs containing no beetles or fungi, or empty screen cylinders. Captures of Heydenia unica Cook and Davis (Hymenoptera: Pteromalidae) and Rhopalicus pulchripennis (Crawford) (Hymenoptera: Pteromalidae) on logs with both G. clavigera and O. montium were greater than those from control treatments. These results suggest that characteristics of tree tissues simultaneously colonized by the two symbiotic fungi facilitate a detectable change in the volatile compounds released from D. ponderosae-attacked trees that may be used by parasitoids to locate hosts.

Résumé

Nous étudions les signaux utilizés par les parasitoïdes pour détecter l’habitat du dendroctone du pin ponderosa, Dendroctonus ponderosae Hopkins (Coleoptera: Curculionidae), en observant l’attrait des parasitoïdes pour des troncs infestés par D. ponderosae, des troncs inoculés par l’un ou les deux champignons symbiotes de D. ponderosae (Grosmannia clavigera (Rob.-Jeff. & R.W. Davidson) Zipfel, Z.W. de Beer & M.J. Wingf. (Ophiostomataceae) et Ophiostoma montium (Rumbold) Arx (Ophiostomataceae)), des troncs ne contenant ni coléoptères ni champignons et des cylindres vides en grillage. Les captures d’Heydenia unica Cook et Davis (Hymenoptera: Pteromalidae) et de Rhopalicus pulchripennis (Crawford) (Hymenoptera: Pteromalidae) sur des troncs portant à la fois G. clavigera et O. montium sont plus importantes que sur les troncs témoins. Ces résultats indiquent que les caractéristiques associées aux tissus des arbres colonizés simultanément par les deux champignons symbiotes entraînent un changement perceptible dans la libération des substances volatiles par les arbres attaqués par D. ponderosae et que ces changements peuvent être utilizés par les parasitoïdes pour repérer leurs hôtes.

[Traduit par la Rédaction]

Type
Articles
Copyright
Copyright © Entomological Society of Canada 2008

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References

Adams, A.S., and Six, D.L. 2007. Temporal variation in mycophagy and prevalence of fungi associated with developmental stages of the mountain pine beetle, Dendroctonus ponderosae. Environmental Entomology, 36: 6472.CrossRefGoogle Scholar
Birgersson, G., and Bergström, G. 1989. Volatiles released from individual spruce bark beetle entrance holes: quantitative variations during the first week of attack. Journal of Chemical Ecology, 15: 24652483.CrossRefGoogle ScholarPubMed
Camors, R.B. Jr., and Payne, T.L. 1972. Response of Heydenia unica (Hymenoptera: Pteromalidae) to Dendroctonus frontalis (Coleoptera: Scolytidae) pheromones and a host-tree terpene. Annals of the Entomological Society of America, 65: 3133.CrossRefGoogle Scholar
Hanssen, H.P. 1993. Volatile metabolites produced by species of Ophiostoma and Ceratocystis. In Ceratocystis and Ophiostoma: taxonomy, ecology, and pathology. Edited by Wingfield, M.S., Seifert, K.A., and Webber, J.F.. APS Press, St. Paul, Minnesota. pp. 117125.Google Scholar
Leufvén, A., Bergström, G., and Falsen, E. 1988. Oxygenated monoterpenes produced by yeasts, isolated from Ips typographus (Coleoptera: Scolytidae) and grown in phloem medium. Journal of Chemical Ecology, 14: 353362.CrossRefGoogle Scholar
Madden, J.L. 1968. Behavioral responses of parasites to the symbiotic fungus associated with Sirex noctilio F. Nature (London), 218: 189190.CrossRefGoogle Scholar
Payne, T.L., Dickens, J.C., and Richerson, J.V. 1984. Insect predator–prey coevolution via enantiomeric specificity in a kairomone–pheromone system. Journal of Chemical Ecology, 10: 487492.CrossRefGoogle Scholar
Pettersson, E.M. 2001. Volatile attractants for three pteromalid parasitoids attacking concealed spruce bark beetles. Chemoecology, 11: 8995.CrossRefGoogle Scholar
Pettersson, E.M., and Boland, W. 2003. Potential parasitoid attractants, volatile composition throughout a bark beetle attack. Chemoecology, 13: 2737.CrossRefGoogle Scholar
Schnee, C., Köllner, T.G., Held, M., Turlings, T.C.J., Gershenzon, J., and Degenhardt, J. 2006. The products of a single maize sesquiterpene synthase form a volatile defense signal that attracts natural enemies of maize herbivores. Proceedings of the National Academy of Sciences, 103: 11291134.CrossRefGoogle Scholar
Six, D.L., and Bentz, B.J. 2007. Temperature determines symbiont abundance in a multipartite bark beetle – fungus ectosymbiosis. Microbial Ecology, 54: 112118.CrossRefGoogle Scholar
Sullivan, B.T., and Berisford, C.W. 2004. Semiochemicals from fungal associates of bark beetles may mediate host location behavior of parasitoids. Journal of Chemical Ecology, 30: 703717.CrossRefGoogle ScholarPubMed
Sullivan, B.T., Pettersson, E.M., Seltmann, K.C., and Berisford, C.W. 2000. Attraction of the bark beetle parasitoid Roptrocerus xylophagorum (Hymenoptera: Pteromalidae) to host-associated olfactory cues. Environmental Entomology, 29: 11381151.CrossRefGoogle Scholar
Upadhyay, H.P. 1981. A monograph of Ceratocystis and Ceratocystiopsis. University of Georgia Press, Athens, Georgia.Google Scholar