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Diet breadth of Gynaephora groenlandica (Lepidoptera: Erebidae): is polyphagy greater in alpine versus Arctic populations?

Published online by Cambridge University Press:  29 May 2014

I.C. Barrio*
Affiliation:
Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E9
D.S. Hik
Affiliation:
Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E9
J.Y. Liu
Affiliation:
Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E9
*
1Corresponding author (e-mail: icbarrio@gmail.com)

Abstract

Gynaephora groenlandica (Wocke) (Lepidoptera: Erebidae) is a cold-adapted species, whose life history traits are dictated by cold and short Arctic summers. We used a recently discovered alpine tundra population in southwestern Yukon, Canada to investigate local adaptations to habitats with different environmental conditions (alpine versus Arctic). Using cafeteria-type experiments and field observations we examined the diet breadth of alpine populations of G. groenlandica beringiana Schmidt and Cannings, and compared these to published data on High Arctic populations of G. groenlandica groenlandica and to the closely related G. rossii Curtis. Gynaephora groenlandica beringiana appears to have a broader diet than High Arctic populations, but similar to that exhibited by alpine populations of G. rossii. Such trends could emerge from reduced synchrony between herbivores and their host plants in less extreme environments, and possibly from a reduced incidence of parasitoids in the life cycle of these populations. Our findings indicate the larval host plant plasticity of G. groenlandica in different environments, and are relevant to predictions regarding the fate of these populations under climate warming scenarios.

Type
Behaviour & Ecology – NOTE
Copyright
© Entomological Society of Canada 2014 

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Footnotes

Subject Editor: Chris Schmidt

References

Bale, J.S., Masters, G.J., Hodkinson, I.D., Awmack, C., Bezemer, T.M., Brown, V.K., et al. 2002. Herbivory in global climate change research: direct effects of rising temperature on insect herbivores. Global Change Biology, 8: 116.CrossRefGoogle Scholar
Barrio, I.C., Hik, D.S., Peck, K., and Bueno, C.G. 2013a. After the frass: foraging pikas select patches previously grazed by caterpillars. Biology Letters, 9: 20130090.Google Scholar
Barrio, I.C., Schmidt, B.C., Cannings, S., and Hik, D.S. 2013b. First records of the Arctic moth Gynaephora groenlandica (Wocke) south of the Arctic Circle – a new alpine subspecies. Arctic, 66: 429434.Google Scholar
Braschler, B. and Hill, J.K. 2007. Role of larval host plants in the climate-driven range expansion of the butterfly Polygonia c-album. Journal of Animal Ecology, 76: 415423.CrossRefGoogle ScholarPubMed
Danks, H.V. 1992. Long life cycles in insects. The Canadian Entomologist, 187: 167187.Google Scholar
Danks, H.V. 1999. Life cycles in polar arthropods – flexible or programmed? European Journal of Entomology, 93: 383403.Google Scholar
Danks, H.V. 2004. Seasonal adaptations in arctic insects. Integrative and Comparative Biology, 44: 8594.Google Scholar
Ferguson, D.C. 1978. The moths of North America north of Mexico, Noctuoidea: Lymantriidae, E.W. Classey Limited and The Wedge Entomological Research Foundation, London, United Kingdom.Google Scholar
Hodkinson, I. 1997. Progressive restriction of host plant exploitation along a climatic gradient: the willow psyllid Cacopsylla groenlandica in Greenland. Ecological Entomology, 22: 4754.CrossRefGoogle Scholar
Høye, T.T. and Forchhammer, M.C. 2008. Phenology of high-Arctic arthropods: effects of climate on spatial, seasonal, and inter-annual variation. Advances in Ecological Research, 40: 299324.CrossRefGoogle Scholar
Kukal, O. and Dawson, T.E. 1989. Temperature and food quality influences feeding behavior, assimilation efficiency and growth rate of Arctic woolly-bear caterpillars. Oecologia, 79: 526532.Google Scholar
Kukal, O. and Kevan, P.G. 1987. The influence of parasitism on the life history of a High Arctic insect, Gynaephora groenlandica (Wöcke) (Lepidoptera: Lymantriidae). Canadian Journal of Zoology, 65: 156163.Google Scholar
MacLean, S.F. and Jensen, T.S. 1985. Food plant selection by insect herbivores in Alaskan Arctic tundra: the role of plant life form. Oikos, 44: 211221.Google Scholar
Mølgaard, P. and Morewood, D. 1996. ITEX insect: Gynaephora groenlandica / G. rossii. In International tundra experiment manual. Edited by U. Molau and P. Mølgaard. Danish Polar Center, Copenhagen, Denmark. Pp. 3436.Google Scholar
Morewood, W.D. 1998. Reproductive isolation in Arctic species of Gynaephora Hübner (Lepidoptera: Lymantriidae). The Canadian Entomologist, 130: 545546.CrossRefGoogle Scholar
Morewood, W.D. 1999. Temperature/development relationships and life history strategies of Arctic Gynaephora species (Lepidoptera: Lymantriidae) and their insect parasitoids (Hymenoptera: Ichneumonidae and Diptera: Tachinidae) with reference to predicted global warming. Ph.D. thesis. University of Victoria, Victoria, British Columbia, Canada.Google Scholar
Morewood, W.D. and Lange, P. 1997. Immature stages of High Arctic Gynaephora species (Lymantriidae) and notes on their biology at Alexandra Fiord, Ellesmere Island, Canada. Journal of Research on the Lepidoptera, 34: 119141.Google Scholar
Morewood, W.D. and Ring, R.A. 1998. Revision of the life history of the High Arctic moth Gynaephora groenlandica (Wocke) (Lepidoptera: Lymantriidae). Canadian Journal of Zoology, 76: 13711381.CrossRefGoogle Scholar
Mulder, C.P.H., Koricheva, J., Huss-Danell, K., Högberg, P., and Joshi, J. 1999. Insects affect relationships between plant species richness and ecosystem processes. Ecology Letters, 2: 237246.Google Scholar
Nylin, S., Nygren, G.H., Söderlind, L., and Stefanescu, C. 2009. Geographical variation in host plant utilization in the comma butterfly: the roles of time constraints and plant phenology. Evolutionary Ecology, 23: 807825.Google Scholar
Pérez-Harguindeguy, N., Díaz, S., Vendramini, F., Cornelissen, J.H.C., Gurvich, D.E., and Cabido, M. 2003. Leaf traits and herbivore selection in the field and in cafeteria experiments. Austral Ecology, 28: 642650.Google Scholar
R Development Core Team 2011. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria.Google Scholar
Roslin, T., Wirta, H., Hopkins, T., Hardwick, B., and Várkonyi, G. 2013. Indirect interactions in the High Arctic. Public Library of Science One, 8: e67367.Google Scholar
Schaefer, P.W. and Castrovillo, P.J. 1979. Gynaephora rossii (Curtis) on Mt. Katahdin, Maine, and Mt. Daisetsu, Japan, and comparisons to records for populations from the Arctic (Lymantriidae). Journal of Research on the Lepidoptera, 18: 241250.Google Scholar
Várkonyi, G. and Roslin, T. 2013. Freezing cold yet diverse: dissecting a high-Arctic parasitoid community associated with Lepidoptera hosts. The Canadian Entomologist, 145: 193218.CrossRefGoogle Scholar
Zuur, A.F., Ieno, E.N., Walker, N.J., Saveliev, A.A., and Smith, G.M. 2009. Mixed effects models and extensions in ecology with R. Springer, New York, New York, United States of America.Google Scholar