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Shifting body weight-fecundity relationship in a capital breeder: maternal effects on egg numbers of the autumnal moth under field conditions

Published online by Cambridge University Press:  29 July 2008

A. Heisswolf ,
T. Klemola ,
T. Andersson  and
K. Ruohomäki
A. Heisswolf*
Affiliation:
Section of Ecology, Department of Biology, University of Turku, FI-20014 Turku, Finland
T. Klemola
Affiliation:
Section of Ecology, Department of Biology, University of Turku, FI-20014 Turku, Finland
T. Andersson
Affiliation:
Section of Ecology, Department of Biology, University of Turku, FI-20014 Turku, Finland Kevo Subarctic Research Institute, University of Turku, FI-20014 Turku, Finland
K. Ruohomäki
Affiliation:
Section of Ecology, Department of Biology, University of Turku, FI-20014 Turku, Finland
*
*Author for correspondence Fax: +358 2 333 6550 E-mail: [email protected]
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Abstract

In the literature, various environmental factors are described as being capable of influencing the reproductive output of insect females irrespective of their body size. Still, female body size or weight is widely used as a proxy for fecundity. In the present study, a seven-year data set on the autumnal moth, Epirrita autumnata (Borkhausen) (Lepidoptera: Geometridae), was used to analyze whether the body weight-fecundity relationship in this capital breeding, cyclic forest defoliating lepidopteran is constant across years. Ambient temperature conditions and density of conspecifics during larval development, the length of the pupal period, as well as moth densities in the parent generation were examined as factors capable of modifying the body weight-fecundity relationship. While the regression slope of potential fecundity (total egg numbers per female) on pupal mass was constant across years, the mean total egg number per given body weight (the regression intercept) was significantly different between years. This residual variance in egg numbers after controlling for the effect of pupal mass was best explained by the pooled geometrid density (autumnal and winter moths) in the parent generation. The total egg number per given body weight decreased with increasing density of geometrid moths in the parent generation. Thus, maternal density effects on offspring fecundity were found in this system. Their rather weak nature suggests, however, that this maternal effect alone does not have the potential of causing cyclic population dynamics in the autumnal moth.

Keywords

Epirrita autumnataLepidopteramaternal density effectsmountain birchpotential fecunditytemperature
Type
Research Paper
Information
Bulletin of Entomological Research , Volume 99 , Issue 1 , February 2009 , pp. 73 - 81
Copyright
Copyright © 2008 Cambridge University Press

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References

Alonso, C., Ruohomäki, K., Riipi, M. & Henriksson, J. (2001) Testing for prerequisites of local adaptation in an insect herbivore, Epirrita autumnata. Écoscience 8, 26–31.CrossRefGoogle Scholar
Awmack, C.S. & Leather, S.R. (2002) Host plant quality and fecundity in herbivorous insects. Annual Review of Entomology 47, 817–844.CrossRefGoogle ScholarPubMed
Bauerfeind, S.S. & Fischer, K. (2005a) Effects of adult-derived carbohydrates, amino acids and micronutrients on female reproduction in a fruit-feeding butterfly. Journal of Insect Physiology 51, 545–554.CrossRefGoogle Scholar
Bauerfeind, S.S. & Fischer, K. (2005b) Effects of food stress and density in different life stages on reproduction in a butterfly. Oikos 111, 514–524.CrossRefGoogle Scholar
Broekhuizen, N., Hassell, M.P. & Evans, H.F. (1994) Common mechanisms underlying contrasting dynamics in two populations of the pine looper moth. Journal of Animal Ecology 63, 245–255.CrossRefGoogle Scholar
Burnham, K.P. & Anderson, D.R. (2002) Model Selection and Multi-model Inference: A Practical Information-Theoretic Approach. 496 pp. New York, Springer.Google Scholar
Calvo, D. & Molina, J.M. (2005) Fecundity–body size relationship and other reproductive aspects of Streblote panda (Lepidoptera: Lasiocampidae). Annals of the Entomological Society of America 98, 191–196.CrossRefGoogle Scholar
Fox, C.W. & Czesak, M.E. (2000) Evolutionary ecology of progeny size in arthropods. Annual Review of Entomology 45, 341–369.CrossRefGoogle ScholarPubMed
Ginzburg, L.R. & Taneyhill, D.E. (1994) Population cycles of forest Lepidoptera: a maternal effect hypothesis. Journal of Animal Ecology 63, 79–92.CrossRefGoogle Scholar
Haukioja, E. (2006) Tree defenses against insects. pp. 279–295in Tuzun, S. & Bent, E. (Eds) Multigenic and Induced Systemic Resistance in Plants. New York, Springer.CrossRefGoogle Scholar
Haukioja, E., Neuvonen, S., Hanhimäki, S. & Niemelä, P. (1988) The autumnal moth in Fennoscandia. pp. 163–178in Berryman, A.A. (Ed.) Dynamics of Forest Insect Populations: Patterns, Causes, and Implications. New York, Plenum Press.CrossRefGoogle Scholar
Haukioja, E., Ossipov, V. & Lempa, K. (2002) Interactive effects of leaf maturation and phenolics on consumption and growth of a geometrid moth. Entomologia Experimentalis et Applicata 104, 125–136.CrossRefGoogle Scholar
Kaitaniemi, P. & Ruohomäki, K. (2001) Sources of variability in plant resistance against insects: free caterpillars show strongest effects. Oikos 95, 461–470.CrossRefGoogle Scholar
Kaitaniemi, P., Ruohomäki, K., Tammaru, T. & Haukioja, E. (1999) Induced resistance of host tree foliage during and after a natural insect outbreak. Journal of Animal Ecology 68, 382–389.CrossRefGoogle Scholar
Kause, A., Saloniemi, I., Haukioja, E. & Hanhimäki, S. (1999) How to become large quickly: quantitative genetics of growth and foraging in a flush feeding lepidopteran larva. Journal of Evolutionary Biology 12, 471–482.CrossRefGoogle Scholar
Kause, A., Saloniemi, I., Morin, J.P., Haukioja, E., Hanhimäki, S. & Ruohomäki, K. (2001) Seasonally varying diet quality and the quantitative genetics of development time and body size in birch feeding insects. Evolution 55, 1992–2001.Google ScholarPubMed
Klemola, T., Ruohomäki, K., Andersson, T. & Neuvonen, S. (2004) Reduction in size and fecundity of the autumnal moth, Epirrita autumnata, in the increase phase of a population cycle. Oecologia 141, 47–56.CrossRefGoogle ScholarPubMed
Klemola, T., Huitu, O. & Ruohomäki, K. (2006) Geographically partitioned spatial synchrony among cyclic moth populations. Oikos 114, 349–359.CrossRefGoogle Scholar
Klemola, T., Klemola, N., Andersson, T. & Ruohomäki, K. (2007) Does immune function influence population fluctuations and level of parasitism in the cyclic geometrid moth? Population Ecology 49, 165–178.CrossRefGoogle Scholar
Klemola, T., Andersson, T. & Ruohomäki, K. (2008) Fecundity of the autumnal moth depends on pooled geometrid abundance without a time lag: implications for cyclic population dynamics. Journal of Animal Ecology 77, 597–604.CrossRefGoogle ScholarPubMed
Klomp, H. (1966) The dynamics of a field population of the pine looper, Bupalus piniarius L. (Lep., Geom.). Advances in Ecological Research 3, 207–305.CrossRefGoogle Scholar
Lill, J.T. & Marquis, R.J. (2001) The effects of leaf quality on herbivore performance and attack from natural enemies. Oecologia 126, 418–428.CrossRefGoogle ScholarPubMed
McMaster, G.S. & Wilhelm, W.W. (1997) Growing degree-days: one equation, two interpretations. Agricultural and Forest Meteorology 87, 291–300.CrossRefGoogle Scholar
Nilssen, A.C. & Tenow, O. (1990) Diapause, embryo growth and supercooling capacity of Epirrita autumnata eggs from northern Fennoscandia. Entomologia Experimentalis et Applicata 57, 39–55.CrossRefGoogle Scholar
Pinheiro, J.C. & Bates, D.M. (2000) Mixed-Effects Models in S and S-PLUS. 528 pp. New York, Springer.CrossRefGoogle Scholar
Pinheiro, J.C., Bates, D.M., DebRoy, S., Sarkar, D. & the R Core team (2007) nlme: Linear and Nonlinear Mixed Effects Models. R package version 3.1–86. Available online: http://www.r-project.org.Google Scholar
Prout, T. & McChesney, F. (1985) Competition among immatures affects their adult fertility: population dynamics. The American Naturalist 126, 521–558.CrossRefGoogle Scholar
R Development Core Team (2007) R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria. ISBN 3-900051-07-0, Available online: http://www.r-project.org.Google Scholar
Ruohomäki, K. (1992) Wing size variation in Epirrita autumnata (Lep., Geometridae) in relation to larval density. Oikos 63, 260–266.CrossRefGoogle Scholar
Ruohomäki, K., Klemola, T., Kaitaniemi, P. & Käär, M. (2003) Crowding-induced responses in a geometrid moth revisited: a field experiment. Oikos 103, 489–496.CrossRefGoogle Scholar
Scoble, M.J. (1992) The Lepidoptera: Form, Function and Diversity. pp. 131–132. Oxford, Oxford University Press.Google Scholar
Stearns, S.C. (1992) The Evolution of Life Histories. 264 pp. Oxford, Oxford University Press.Google Scholar
Steigenga, M.J. & Fischer, K. (2007) Ovarian dynamics, egg size, and egg number in relation to temperature and mating status in a butterfly. Entomologia Experimentalis et Applicata 125, 195–203.CrossRefGoogle Scholar
Tammaru, T. & Haukioja, E. (1996) Capital breeders and income breeders among Lepidoptera – consequences to population dynamics. Oikos 77, 561–564.CrossRefGoogle Scholar
Tammaru, T., Kaitaniemi, P. & Ruohomäki, K. (1995) Oviposition choices of Epirrita autumnata (Lepidoptera: Geometridae) in relation to its eruptive population dynamics. Oikos 74, 296–304.CrossRefGoogle Scholar
Tammaru, T., Kaitaniemi, P. & Ruohomäki, K. (1996a) Realized fecundity in Epirrita autumnata (Lepidoptera: Geometridae): relation to body size and consequences to population dynamics. Oikos 77, 407–416.CrossRefGoogle Scholar
Tammaru, T., Ruohomäki, K. & Saikkonen, K. (1996b) Components of male fitness in relation to body size in Epirrita autumnata (Lepidoptera: Geometridae). Ecological Entomology 21, 185–192.CrossRefGoogle Scholar
Tenow, O. (1972) The outbreaks of Oporinia autumnata Bkh. and Operophthera spp. (Lep., Geometridae) in the Scandinavian mountain chain and northern Finland 1862–1968. Zoologiska Bidrag från Uppsala, Supplement 2, 1–107.Google Scholar
Tenow, O. & Nilssen, A.C. (1990) Egg cold hardiness and topoclimatic limitations to outbreaks of Epirrita autumnata in northern Fennoscandia. Journal of Applied Ecology 27, 723–734.CrossRefGoogle Scholar
Tenow, O., Nilssen, A.C., Bylund, H. & Hogstad, O. (2007) Waves and synchrony in Epirrita autumnata/Operophtera brumata outbreaks. I. Lagged synchrony: regionally, locally and among species. Journal of Animal Ecology 76, 258–268.CrossRefGoogle ScholarPubMed
van Asch, M. & Visser, M.E. (2007) Phenology of forest caterpillars and their host trees: the importance of synchrony. Annual Review of Entomology 52, 37–55.CrossRefGoogle ScholarPubMed
Virtanen, T. & Neuvonen, S. (1999) Performance of moth larvae on birch in relation to altitude, climate, host quality and parasitoids. Oecologia 120, 92–101.CrossRefGoogle ScholarPubMed