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Temperature and food quality effects on growth, consumption and post-ingestive utilization ef.ciencies of the forest tent caterpillar Malacosoma disstria (Lepidoptera: Lasiocampidae)

Published online by Cambridge University Press:  09 March 2007

K.R. Levesque ,
M. Fortin  and
Y. Mauffette
K.R. Levesque*
Affiliation:
Groupe de Recherche en Écologie Forestière interuniversitaire (GREFI), Université du Québec à Montréal, C.P. 8888, Succ. A. Montréal, QC, Canada, H3C 3P8
M. Fortin
Affiliation:
Groupe de Recherche en Écologie Forestière interuniversitaire (GREFI), Université du Québec à Montréal, C.P. 8888, Succ. A. Montréal, QC, Canada, H3C 3P8
Y. Mauffette
Affiliation:
Groupe de Recherche en Écologie Forestière interuniversitaire (GREFI), Université du Québec à Montréal, C.P. 8888, Succ. A. Montréal, QC, Canada, H3C 3P8
*
*Groupe Interuniversitaire de Recherches Océanographiques du Québec (GIROQ), Université Leval, Pavillon Vachon, QC, CanadaG1K 7P4 Fax: (418) 656 2339 E-mail: [email protected]
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Abstract

Temperature and food quality can both influence growth rates, consumption rates, utilization efficiencies and developmental time of herbivorous insects. Gravimetric analyses were conducted during two consecutive years to assess the effects of temperature and food quality on fourth instar larvae of the forest tent caterpillar Malacosoma disstria Hübner. Larvae were reared in the laboratory at three different temperatures (18, 24 and 30°C) and on two types of diet; leaves of sugar maple trees Acer saccharum Marsh. located at the forest edge (sun-exposed leaves) or within the forest interior (shade-exposed leaves). In general, larvae reared at 18°C had lower growth rates and lower consumption rates than larvae reared at the warmer temperatures (24 and 30°C). Moreover, the duration of the instar decreased significantly with increasing temperatures. Type of diet also affected the growth rates and amount of food ingested by larvae but did not affect the duration of the instar. Larvae fed sun-exposed leaves consumed more food and gained higher biomasses. Values of approximate digestibility and efficiency of conversion of ingested food were also higher when larvae were fed sun-exposed leaves. Higher growth rates with increasing temperatures were primarily the result of the shorter stadium duration. The higher growth rates of larvae fed sun-exposed leaves were possibly the result of stimulatory feeding and consequently greater food intake and also a more efficient use of food ingested. This study suggests that the performance of M. disstria caterpillars could be enhanced by warmer temperatures and higher leaf quality.

Type
Research Article
Information
Bulletin of Entomological Research , Volume 92 , Issue 2 , April 2002 , pp. 127 - 136
Copyright
Copyright © Cambridge University Press 2002

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References

Albert, P.J. & Parisella, S. (1985) Feeding preferences of eastern spruce budworm larvae in two-choice test with combinations of host plant extracts. Entomologia Experimentalis et Applicata 38, 221–225.CrossRefGoogle Scholar
Albert, P.J. & Parisella, S. (1988) Feeding preferences of eastern spruce budworm larvae in two-choice tests with extracts of mature foliage and with pure amino acids. Journal of Chemical Ecology 14, 1649–1656.CrossRefGoogle ScholarPubMed
Ali, A., Luttrel, R.G. & Schneider, J.C. (1990) Effects of temperature and larval diet on development of the fall armyworm (Lepidoptera: Noctuidae). Annals of the Entomological Society of America 83, 725–733.CrossRefGoogle Scholar
Ayres, M.P. (1993) Plant defense, herbivory and climate change. pp. 75–94 in Kareiva, P.K., Kingsolver, J.G. & Huey, B.B. (Eds), Biotic interactions and global change. Sunderland,Massachusetts, Sinauer Associates.Google Scholar
Ayres, M.P. & MacClean, S.F. (1987) Molt as a component of insect development: Galerucella sagittariae (Chrysomelidae) and Epirrita autumnata (Geometridae). Oikos 48, 273–279.CrossRefGoogle Scholar
Ayres, M.P. & MacClean, S.F. (1987) Development of birch leaves and the growth energetics of Epirrita autumnata (Geometridae). Ecology 68, 558–568.CrossRefGoogle Scholar
Beck, S.D. (1991) Thermoperiodism. pp. 199–227in Lee, R.E. Jr. & Denlinger, D.L. (Eds) Insects at low temperature. New York, Chapman & Hall.CrossRefGoogle Scholar
Bernays, E.A. & Chapman, R.F. (1994) Host-plant selection by phytophagous insects. pp. 95–165. New York, Chapman & Hall.CrossRefGoogle Scholar
Bidon, Y. (1993) Influence des sucres solubles et de l'azote sur la croissance, le développement et l'utilisation de la nourriture par la tordeuse des bourgeons de l'épinette [Choristoneura fumiferana (Clem.)]. 60 pp. Ms thesis. Université Laval, Ste-Foy, Québec, Canada.Google Scholar
Bryant, J.P., Chapin, F.S. III & Klein, D.R. (1983) Carbon/nutrient balance of boreal plants in relation to vertebrate herbivory. Oikos 40, 357–368.CrossRefGoogle Scholar
Clancy, K.M. (1992) Response of western spruce budworm (Lepidoptera: Tortricidae) to increased nitrogen in artificial diets. Environmental Entomology 21, 331–334.CrossRefGoogle Scholar
Denslow, J.S., Shultz, J.C., Vitousek, P.M. & Strain, B.R. (1990) Growth responses of tropical shrubs to treefall gap environments. Ecology 71, 165–179.CrossRefGoogle Scholar
Dethier, V.G. (1947) Chemical insect attractants and repellents. 289 pp. Philadelphia, Blakiston.Google Scholar
Dudt, J.F. & Shure, D.J. (1994) The influence of light and nutrients on foliar phenolics and insect herbivory. Ecology 75, 86–98.CrossRefGoogle Scholar
Ellsworth, D.S. & Reich, P.B. (1993) Canopy structure and vertical patterns of photosynthesis and related leaf traits in a deciduous forest. Oecologia 96, 169–178.CrossRefGoogle Scholar
Field, C. & Mooney, H.A. (1986) The photosynthesis-nitrogen relationship in wild plants. pp. 25–56 in Givnish, T. (Ed.) On the economy of plant form and function. Cambridge, Cambridge University Press.Google Scholar
Fortin, M. (2000) Effets de l'hétérogénéité de la nourriture et de la variation de la température sur la performance biologique de la livrée des forêts (Malacosoma disstria Hbn.) s'alimentant dans une érablière. 145 pp. PhD thesis, Université du Québec à Montréal, Montréal, Québec, Canada.Google Scholar
Fortin, M. & Mauffette, Y. (2001) Forest edge effects on the biological performance of the forest tent caterpillar (Lepidoptera: Lasiocampidae) in sugar maple stands. Ecoscience 8, 164–172.CrossRefGoogle Scholar
Futuyma, D.J. & Saks, M.E. (1981) The effects of variation in host plant on the growth of an oligophagous insect, Malacosoma americanum and its polyphagous relative, Malacosoma disstria. Entomologia Experimentalis et Applicata 30, 163–168.CrossRefGoogle Scholar
Grandtner, M.M. (1966) La végétation forestière du Québec méridional. Les Presses de l'Université Laval, Québec.Google Scholar
Grisdale, D.G. (1968) A method for reducing incidence of virus infection in insect rearings. Journal of Invertebrate Pathology 10, 425.CrossRefGoogle Scholar
Harrison, S. (1987) Treefall gaps versus forest understory as environment for a defoliating moth on a tropical forest shrub. Oecologia 72, 65–68.CrossRefGoogle ScholarPubMed
Karowe, D.N. (1989) Differential effect of tannic acid on two tree-feeding Lepidoptera: implications for theories of plant anti-herbivore chemistry. Oecologia 80, 507–512.CrossRefGoogle ScholarPubMed
Kingsolver, J.G. & Woods, H.A. (1997) Thermal sensitivity of growth and feeding in Manduca sexta caterpillars. Physiological Zoology 70, 631–638.CrossRefGoogle ScholarPubMed
Lincoln, D.E. & Mooney, H.A. (1984) Herbivory on Diplacus aurantiacus shrubs in sun and shade. Oecologia 64, 173–176.CrossRefGoogle ScholarPubMed
Louda, S.V. & Rodman, J.E. (1996) Insect herbivory as a major factor in the shade distribution of a native crucifer (Cardamine cordifolia A. Gray, bittercress). Journal of Ecology 84, 229–237.CrossRefGoogle Scholar
Mattson, W.J. (1980) Herbivory in relation to plant nitrogen content. Annual Review of Ecology and Systematics 11, 119–161.CrossRefGoogle Scholar
Mattson, W.J. & Scriber, J.M. (1987) Nutritional ecology of insects folivores of woody plants: nitrogen, water, fiber, and mineral considerations. pp. 105–146 in Slansky, F. Jr. & Rodriguez, J.G. (Eds) Nutritional ecology of insects, mites, spiders, and related invertebrates. New York, Wiley & Sons.Google Scholar
Mole, S. & Waterman, P.G. (1988) Light-induced variation in phenolic levels in foliage of rain-forest plants. II. Potential significance to herbivores. Journal of Chemical Ecology 14, 23–34.CrossRefGoogle ScholarPubMed
Nichols-Orians, C.M. (1991) The effects of light on foliar chemistry, growth and susceptibility of seedlings of a canopy tree to an attine ant. Oecologia 86, 552–560.CrossRefGoogle Scholar
Parry, W.H., Kelly, J.M. & McKillop, A.R. (1990) The role of nitrogen in the feeding strategy of Strophosomus melanogrammus (Forster) (Col., Curculionidae) in a mixed woodland habitat. Journal of Applied Entomology 109, 367–376.CrossRefGoogle Scholar
Ratte, H.T. (1984) Temperature and insect development. pp. 33–66 in Hoffmann, K.H. (Ed.) Environmental physiology and biochemistry of insects. Berlin, Springer.CrossRefGoogle Scholar
Raubenheimer, D. & Simpson, S.J. (1992) Analysis of covariance: an alternative to nutritional indices. Entomologia Experimentalis et Applicata 62, 221–231.CrossRefGoogle Scholar
Raupp, M.J. & Denno, R.F. (1983) Leaf age as a predictor of herbivore distribution and abundance. pp. 9–124in Denno, R.F. & McClure, M.S. (Eds) Variable plants and herbivores in natural and managed systems. New York, Academic Press.Google Scholar
Reynolds, S.E. & Nottingham, S.F. (1985) Effects of temperature on growth and efficiency of food utilization in fifth-instar caterpillars of the tobacco hornworm. Manduca sexta. Journal of Insect Physiology 31, 129–134.CrossRefGoogle Scholar
SAS Institute Inc. (1998) SAS/STATtm guide for personal computers. SAS Institute inc. Version 6.03 edition, Cary, North Carolina.Google Scholar
Schramm, U. (1972) Temperature-food interaction in herbivorous insects. Oecologia 9, 399–402.CrossRefGoogle ScholarPubMed
Schroeder, L. & Lawson, J. (1992) Temperature effects on the growth and dry matter budgets of Malacosoma americanum. Journal of Insect Physiology 38, 743–749.CrossRefGoogle Scholar
Scriber, J.M. (1984) Host plant suitability. pp. 159–202 in Bell, W. & Cardé, R.T. (Eds) Chemical ecology of insects. London, Chapman & Hall.CrossRefGoogle Scholar
Scriber, J.M. & Lederhouse, R.C. (1983) Temperature as a factor in the development and feeding ecology of tiger swallowtail caterpillars, Papillio glaucus (Lepidoptera). Oikos 40, 95–102.CrossRefGoogle Scholar
Scriber, J.M. & Slansky, F. (1981) The nutritional ecology of immature insects. Annual Review of Entomology 26, 183–211.CrossRefGoogle Scholar
Slansky, F. (1993) Nutritional ecology: the fundamental quest for nutrients. pp. 29–91 in Stamp, N.E. & Casey, T.M. (Eds) Caterpillars: ecological and evolutionary constraints on foraging. New York, Chapman & Hall.Google Scholar
Slansky, F. & Scriber, J.M. (1985) Food consumption and utilization. pp. 87–163 in Kerkut, G.A. & Gilbert, L.I. (Eds) Comparative insect physiology biochemistry and pharmacology. Oxford, Pergamon Press.Google Scholar
Stamp, N.E. (1990) Growth versus molting time of caterpillars as a function of temperature, nutrient concentration and the phenolic rutin. Oecologia 82, 107–113.CrossRefGoogle ScholarPubMed
Stamp, N.E. (1993) A temperate region view of the interaction of temperature, food quality, and predators on caterpillars. pp. 478–508 in Stamp, N.E. (Ed.) Caterpillars: ecological and evolutionary constraints on foraging. New York, Chapman & Hall.Google Scholar
Stamp, N.E. & Bowers, M.D. (1990) Variation in food quality and temperature constrain foraging of gregarious caterpillars. Ecology 71, 1031–1039.CrossRefGoogle Scholar
Stamp, N.E. & Bowers, M.D. (1994) Effect of temperature and leaf age on growth versus moulting time of a generalist caterpillar fed plantain (Plantago lanceolata). Ecological Entomology 19, 199–206.CrossRefGoogle Scholar
Stamp, N.E. & Horwath, K.L. (1992) Interactive effects of temperature and concentration of the flavanol rutin on growth, molt and food utilization of Manduca sexta caterpillars. Entomologia Experimentalis et Applicata 64, 135–150.CrossRefGoogle Scholar
Stamp, N.E. & Yang, Y. (1996) Response of insect herbivores to multiple allelochemicals under different thermal regime. Ecology 77, 1088–1102.CrossRefGoogle Scholar
Stamp, N.E., Erskine, T. & Paradise, C.J. (1991) Effects of rutin-fed caterpillars on an invertebrate predator depend on temperature. Oecologia 88, 289–295.CrossRefGoogle Scholar
Stamp, N.E., Temple, M.P., Traugott, M.S. & Wilkens, R.T. (1994) Temperature-allelochemicals interactive effects on performance of Manduca sexta caterpillars. Entomologia Experimentalis & Applicata 73, 199–210.CrossRefGoogle Scholar
Taylor, F. (1981) Ecology and evolution of physiological time in insects. American Naturalist 117, 1–23.CrossRefGoogle Scholar
Thomas, W.M. (1991) Modeling the effects of temperature and gossypol concentration on developmental rate of Helicoverpa zea (Boddie) (Lepidoptera: Noctuidae). Journal of Economical Entomology 84, 466–469.CrossRefGoogle Scholar
Waldbauer, G.P. (1968) The consumption and utilization of food by insects. Advances in Insect Physiology 5, 229–288.CrossRefGoogle Scholar
White, T.C.R. (1984) The abundance of invertebrate herbivores in relation to the availability of nitrogen in stressed food plants. Oecologia 63, 90–105.CrossRefGoogle Scholar
Yang, Y. & Stamp, N.E. (1995) Simultaneous effects of night-time temperature and an allelochemical on performance of a Solanaceae specialist caterpillar. Oecologia 104, 225–233.CrossRefGoogle Scholar
Yang, Y. & Stamp, N.E. (1996) Simultaneous effects of temperature and multiple allelochemicals on the performance of a Solanaceae specialist caterpillar (Manduca sexta). Ecoscience 3, 81–92.CrossRefGoogle Scholar