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Insights into herbivore distribution and abundance: oviposition preferences of western hemlock and phantom hemlock loopers

Published online by Cambridge University Press:  03 January 2012

Martin J. Steinbauer  and
Allan L. Carroll
Martin J. Steinbauer
Affiliation:
Cooperative Research Centre for Sustainable Production Forestry, Commonwealth Scientific and Industrial Research Organization Entomology, Canberra, and Department of Zoology, La Trobe University, Melbourne, Victoria 3086, Australia
Allan L. Carroll*
Affiliation:
Cooperative Research Centre for Sustainable Production Forestry, Commonwealth Scientific and Industrial Research Organization Entomology, Canberra, and Department of Zoology, La Trobe University, Melbourne, Victoria 3086, Australia
*
3Corresponding author (e-mail: Allan.Carroll@ubc.ca).
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Abstract

Knowledge of the factors affecting host selection by herbivorous insects is essential to predictions of their distribution and abundance over landscapes. In the laboratory, we studied the oviposition preferences of two eruptive loopers (Lepidoptera: Geometridae) native to western Canada (western hemlock looper, Lambdina fiscellaria lugubrosa (Hulst), and phantom hemlock looper, Nepytia phantasmaria (Strecker)) for different species and condition of hosts. When offered a choice, phantom hemlock loopers laid nearly three times as many eggs on western hemlock, Tsuga heterophylla (Raf.) Sarg. (Pinaceae) as on either western redcedar, Thuja plicata Donn ex D. Don (Cupressaceae) or western white pine, Pinus monticola Douglas ex D. Don (Pinaceae). Western hemlock loopers were less specific, laying equal numbers of eggs on western hemlock and western redcedar, though fewer eggs were deposited on western white pine when compared with western hemlock. When offered western hemlock trees grown under different nutrient and shading regimes, phantom hemlock loopers preferred to oviposit on high nutrient hosts, irrespective of shading; western hemlock loopers exhibited a preference for high-nutrient hosts only if they were grown without shading. These patterns of host preference can be combined with information regarding forest composition to help quantify the conditional probability of western and phantom hemlock looper distibution and abundance.

Résumé

Il est essentiel de connaître les facteurs qui affectent la sélection d'hôtes par les insectes herbivores afin de prédire leur répartition et leur abondance dans les paysages. Nous avons étudié au laboratoire les préférences de sites de ponte chez deux arpenteuses épidémiques (Lepidoptera : Geometridae) indigènes de l'Ouest canadien (l'arpenteuse de la pruche de l'Ouest, Lambdina fiscellaria lugubrosa (Hulst), et l'arpenteuse verte de la pruche, Nepytia phantasmaria (Strecker)) sur différentes espèces et conditions d'hôtes. En présence d'un choix, les arpenteuses vertes de la pruche pondent presque trois fois plus d'œufs sur la pruche de l'Ouest, Tsuga heterophylla (Raf.) Sarg. (Pinaceae) que sur le thuya géant, Thuya plicata Donn ex D. Don (Cupressaceae) et le pin argenté, Pinus monticola Douglas ex D. Don (Pinaceae). Les arpenteuses de la pruche de l'Ouest sont moins spécifiques et pondent des nombres égaux d'œufs sur la pruche de l'Ouest et le thuya géant, bien qu'elle pondent moins d'œufs sur le pin argenté que sur la pruche de l'Ouest. Lorsqu'on leur présente des pruches de l'Ouest qui ont crû sous divers régimes de nutriments et d'ombre, les arpenteuses vertes de la pruche préfèrent pondre sur des arbres élevés dans un régime riche en nutriments, sans égard aux conditions d'ombre; les arpenteuses de la pruche de l'Ouest montrent une préférence pour les hôtes de régime riche en nutriments seulement si ceux-ci ont été élevés sans ombrage. On peut combiner ces patrons de préférence d'hôtes à des données sur la composition forestière pour aider à calculer la probabilité conditionnelle de la répartition et de l'abondances des arpenteuses de la pruche de l'ouest et des arpenteuses vertes de la pruche.

[Traduit par la Rédaction]

Type
Articles
Information
The Canadian Entomologist , Volume 143 , Issue 1 , February 2011 , pp. 72 - 81
Copyright
Copyright © Entomological Society of Canada 2011

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References

Alfaro, R.I., Taylor, S., Brown, G., and Wegwitz, E. 1999. Tree mortality caused by the western hemlock looper in landscapes of central British Columbia. Forest Ecology and Management, 124: 285–291. doi:10.1016/S0378-1127(99)00073-0.CrossRefGoogle Scholar
Alonso, C., and Herrera, C.M. 1996. Variation in herbivory within and among plants of Daphne laureola (Thymelaeaceae): correlation with plant size and architecture. Journal of Ecology, 84: 495–502. doi:10.2307/2261472.CrossRefGoogle Scholar
Barron, A.B. 2001. The life and death of Hopkins' host-selection principle. Journal of Insect Behavior, 14: 725–737. doi: 10.1023/A:1013033332535.CrossRefGoogle Scholar
Bernays, E.A., and Chapman, R.F. 1994. Host-plant selection by phytophagous insects. Chapman and Hall, New York.CrossRefGoogle Scholar
Borecky, N., and Otvos, I.S. 2001. Coarse-scale hazard rating of western hemlock looper in British Columbia. In Proceedings - Integrated management and dynamics of forest defoliating insects, August 15–19, 1999, Victoria BC, Canada. Edited by Liebhold, A.M., McManus, M.L., Otvos, I.S., and Fosbroke, S.L.C.. USDA Forest Service, General Technical Report NE-277. pp. 6–15.Google Scholar
Carolin, V.M., and Lejeune, R.R. 1967. Western hemlock looper, Lambdina fiscellaria lugubrosa Hulst. In Important forest insects and diseases of mutual concern to Canada, the United States and Mexico. Edited by Davidson, A.G. and Prentice, R.M.. North American Forestry Commission, Ottawa, Ontario. pp. 123–125.Google Scholar
Carroll, A.L. 1999. Physiological adaptation to temporal variation in conifer foliage by a caterpillar. The Canadian Entomologist, 131: 659–669. doi:10.4039/Ent131659-5.CrossRefGoogle Scholar
Farrar, J.L. 1995. Trees in Canada. Fitzhenry and Whiteside Ltd., Ottawa, Ontario.Google Scholar
Fujiyama, N., Koizumi, T., and Katakura, H. 2003. Conspecific thistle plant selection by a herbivorous ladybird beetle, Epilachna pustulosa. Entomologia Experimentalis et Applicata, 108: 33–42. doi: 10.1046/j.1570-7458.2003.00063.x.CrossRefGoogle Scholar
Furniss, R.L., and Carolin, V.M. 1977. Western forest insects. USDA, Forest Service, Washington.CrossRefGoogle Scholar
Harris, J.W.E., Dawson, A.F., and Brown, R.G. 1982. The western hemlock looper in British Columbia, 1911–1980. Canadian Forest Service, Victoria, British Columbia.Google Scholar
Hawkins, B.J., Burgess, D., and Mitchell, A.K. 2005. Growth and nutrient dynamics of western hemlock with conventional or exponential green-house fertilization and planting in different fertility conditions. Canadian Journal of Forest Research, 35: 1002–1016. doi: 10.1139/x05-026.CrossRefGoogle Scholar
Hébert, C., Jobin, L., Auger, M., and Dupoint, A. 2003. Oviposition traps to survey eggs of Lambdina fiscellaria (Lepidoptera: Geometridae). Journal of Economic Entomology, 96: 768–776. PMID: 12852615 doi: 10.1603/0022-0493-96.3.768.CrossRefGoogle ScholarPubMed
Herms, D.A., and Mattson, W.J. 1992. The dilemma of plants: to grow or defend. Quarterly Review of Biology, 67: 283–335. doi:10.1086/417659.CrossRefGoogle Scholar
Hopping, G.R. 1934. An account of the western hemlock looper, Ellopia somniaria Hulst, on conifers in British Columbia. Scientific Agriculture, 15: 12–28.Google Scholar
Jaenike, J. 1978. On optimal oviposition behaviour in phytophagous insects. Theoretical Population Biology, 14: 350–356. PMID:751265 doi:10.1016/0040-5809(78)90012-6.CrossRefGoogle ScholarPubMed
Janz, N., Söderlind, L., and Nylin, S. 2009. No effect of larval experience on adult host preferences in Polygonia c-album (Lepidoptera: Nymphalidae): on the persistence of Hopkins' host selection principle. Ecological Entomology, 34: 50–57. doi: 10.1111/j.1365-2311.2008.01041.x.CrossRefGoogle Scholar
Keen, F.P. 1952. Insect enemies of western forests. USDA Forest Service, Miscellaneous Publication No. 273, Washington, USA.CrossRefGoogle Scholar
Kimmins, J.P. 1987. Forest ecology. MacMillan Publishing Company, New York.Google Scholar
Kinghorn, J.M. 1954. The effect of stand composition on the mortality of various conifers caused by defoliation by the western hemlock looper on Vancouver Island, British Columbia. Forestry Chronicle, 30: 380–400.CrossRefGoogle Scholar
Koot, H.P. 1994. Western hemlock looper. Forest Pest Leaflet 21. Natural Resources Canada, Canadian Forest Service, Pacific Forestry Centre, Victoria, British Columbia.Google Scholar
Kozlowski, T.T. 1971. Growth and development of trees. Volume I: Seed germination, ontogeny and shoot growth. Academic Press, New York.Google Scholar
Kranabetter, J.M., Banner, A., and Shaw, J. 2003. Growth and nutrition of three conifer species across site gradients of north coastal British Columbia. Canadian Journal of Forest Research, 33: 313–324. doi: 10.1139/x02-188.CrossRefGoogle Scholar
Mailly, D., and Kimmins, J.P. 1997. Growth of Pseudotsuga menziesii and Tsuga heterophylla seedlings along a light gradient: resource allocation and morphological acclimation. Canadian Journal of Botany, 75: 1424–1435. doi: 10.1139/b97-857.CrossRefGoogle Scholar
Mayhew, P.J. 1997. Adaptive patterns of host-plant selection by phytophagous insects. Oikos, 79: 417–428. doi:10.2307/3546884.CrossRefGoogle Scholar
Moffett, M.W. 2001. The nature and limits of canopy biology. Selbyana, 22: 155–179.Google Scholar
Nahrung, H.F., and Allen, G.R. 2003. Intra-plant host selection, oviposition preference and larval survival of Chrysophtharta agricola (Chapuis) (Coleoptera: Chrysomelidae: Paropsini) between foliage types of a heterophyllous host. Agricultural and Forest Entomology, 5: 155–162. doi: 10.1046/j.1461-9563.2003.00172.x.CrossRefGoogle Scholar
Nothnagle, P.J., and Schultz, J.C. 1987. What is a forest pest? In Insect outbreaks. Edited by Barbosa, P. and Schultz, J.C.. Academic Press, San Diego, California. pp. 59–80.CrossRefGoogle Scholar
Prentice, R.M. 1963. Forest Lepidoptera of Canada recorded by the Forest Insect Survey. Volume 3: Lasiocampidae, Thyatiridae, Drepanidae, Geometridae. Forest Entomology and Pathology Branch, Canadian Department of Forestry, Publication 1013, Ottawa, Ontario.Google Scholar
Price, P.W. 1994. Phylogenetic constraints, adaptive syndromes, and emergent properties: from individuals to population dynamics. Researches in Population Ecology, 36: 3–14. doi:10.1007/BF02515079.CrossRefGoogle Scholar
Price, P.W. 2003. Macroevolutionary theory on macroecological patterns. Cambridge University Press, Cambridge.Google Scholar
Scheirs, J., and De Bruyn, L. 2002. Integrating optimal foraging and optimal oviposition theory in plant-insect research. Oikos, 96: 187–191. doi: 10.1034/j.1600-0706.2002.960121.x.CrossRefGoogle Scholar
Shore, T.L. 1990. Recommendations for sampling and extracting the eggs of the western hemlock looper, Lambdina fiscellaria lugubrosa (Lepidoptera: Geometridae). Journal of the Entomological Society of British Columbia, 87: 25–30.Google Scholar
S-PLUS 6. 2001. S-PLUS 6 for Windows Guide to Statistics, Volume 1. Insightful Corporation, Seattle, Washington.Google Scholar
Steinbauer, M.J., Clarke, A.R., and Madden, J.L. 1998. Oviposition preference of a Eucalyptus herbivore and the importance of leaf age on inter-specific host choice. Ecological Entomology, 23: 201–206. doi: 10.1046/j.1365-2311.1998.00122.x.CrossRefGoogle Scholar
Steinbauer, M.J. 2002. Oviposition preference and neonate performance of Mnesampela privata in relation to heterophylly in Eucalyptus dunnii and E. globulus. Agricultural and Forest Entomology, 4: 245–253. doi: 10.1046/j.1461-9563. 2002.00151.x.CrossRefGoogle Scholar
Thomson, M.G. 1957. Appraisal of western hemlock looper infestations. Forestry Chronicle, 33: 141–147.CrossRefGoogle Scholar
Thompson, J.N., and Pellmyr, O. 1991. Evolution of oviposition behaviour and host preference in Lepidoptera. Annual Review of Entomology, 36: 65–89. doi:10.1146/annurev.en.36.010191.000433.CrossRefGoogle Scholar
Wainhouse, D. 2005. Ecological methods in forest pest management. Oxford University Press, Oxford, New York.Google Scholar
Waters, W.E., and Stark, R.W. 1980. Forest pest management: concept and reality. Annual Review of Entomology, 25: 479–509. doi:10.1146/annurev. en.25.010180.002403.CrossRefGoogle Scholar
Wickman, B.E., and Hunt, R.H. 1969. Biology of the phantom hemlock looper on Douglas-fir in California. Journal of Economic Entomology, 62: 1046–1050.CrossRefGoogle Scholar
Zimmerman, M.H., and Brown, C.L. 1971. Trees: structure and function. Springer-Verlag, New York.CrossRefGoogle Scholar