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Adaptive variation in growth rate: life history costs and consequences in the speckled wood butterfly,Pararge aegeria

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Abstract

An important assumption made in most lifehistory theory is that there is a trade-off between age and size at reproduction. This trade-off may, however, disappear if growth rate varies adaptively. The fact that individuals do not always grow at the maximum rate can only be understood if high growth rates carry a cost. This study investigates the presence and nature of such costs inPararge aegeria. Five females from two populations with known differences in life history (south Sweden and Maderia) were allowed to oviposit in the laboratory and their offspring were reared in environmental chambers under conditions leading to direct development. We measured several aspects of life history, including development times, pupal and adult weights, growth rate, female fecundity, longevity and larval starvation endurance. In both populations there seemed to be genetic variation in growth rate. There was no evidence for a trade-off between age and size at pupation. As predicted, larvae with high growth rates also lost weight at a relatively higher rate during starvation. High weight-loss rates were furthermore associated with a lower probability of surviving when food became available again. This is apparently the first physiological trade-off with growth rate that has been experimentally demonstrated. In both populations there were significant differences in growth rate between the sexes, but the populations differed in which sex was growing at the highest rate. In Sweden males had higher growth rates than females, whereas the reverse was true for Madeira. These patterns most likely reflect differences in selection for protandry, in turn caused by differences in seasonality between Sweden and Madeira. Together with the finding that males had shorter average longevity than females in the Swedish, but not in the Maderiran, population, this indicates that a lower adult quality also may be a cost of high growth rate. We argue that for the understanding of life history variation it is necessary to consider not only the two dimensions of age and size, but also to take into full account the triangular nature of the relationship between size, time and growth rate.

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References

  • Case TJ (1978) On the evolution and adaptive significance of postnatal growth rates in the terrestrial vertebrates. Q Rev Biol 53: 243–282

    Google Scholar 

  • Clutton-Brock TH, Albon SD, Guinness FE (1985) Parental investment and sex differences in juvenile mortality in birds and mammals. Nature 313:131–133

    Google Scholar 

  • Conover DO, Present TMC (1990) Countergradient variation in growth rate: compensation for length of the growing season among Atlantic silversides from different latitudes. Oecologia 83:316–324

    Google Scholar 

  • Crowl TA, Covich AP (1990) Predator-induced life-history shifts in a freshwater snail. Science 247:949–951

    Google Scholar 

  • Fraser DF, Gilliam JF (1992) Nonlethal impacts of predator invasion: facultative suppression of growth and reproduction. Ecology 73:959–970

    Google Scholar 

  • Gebhardt MD, Stearns SC (1988) Reaction norms for development time and weight at eclosion inDrosophila mercatorum. J Evol Biol 1:335–354

    Google Scholar 

  • Gunnarsson B, Johnsson J (1990) Protandry and moulting in the spider Pityohyphantes phrygianus. Oikos 59:205–212

    Google Scholar 

  • Higgins LG (1977) The speckled wood (Pararge aegeria L.) in Madeira. Entomol Rec J Var 89:22–23

    Google Scholar 

  • Higgins LG, Hargreaves B (1983) The butterflies of Britain and Europe. Collins, London

    Google Scholar 

  • Lima S, Dill LM (1990) Behavioral descision made under the risk of predation: a reveiw and prospectus. Can J Zool 68:619–640

    Google Scholar 

  • Negus NC, Berger PJ (1992) Phenotypic plasticity of the montane vole (Microtus montanus) in unpredictable environments. Can J Zool 70:2121–2124

    Google Scholar 

  • Niewiarowski PH, Roosenburg W (1993) Reciprocal transplant reveals sources of variation in growth rates of the lizardSceloporus undulatus. Ecology 74:1992–2002

    Google Scholar 

  • Nylin S, Wickman P-O, Wiklund C (1989) Seasonal plasticity in growth and development of the speckled wood butterfly,Pararge aegeria (Satyrinae). Biol J Linn Soc 38:155–171

    Google Scholar 

  • Nylin S, Wiklund C, Wickman P-O, Garcia-Barros E (1993) Absence of trade-offs between sexual size dimorphism and early male emergence in a butterfly. Ecology 74:1414–1427

    Google Scholar 

  • Owen DF, Shreeve TG, Smith AG (1986) Colonization of Madeira by the speckled wood butterfly,Pararge aegeria (Satyridae), and its impact on the endemicPararge xiphia. Ecol Entomol 11:349–352

    Google Scholar 

  • Perrin N, Rubin JF (1990) On dome-shaped norms of reaction for size-to-age at maturity in fishes. Funct Ecol 4 53–57

    Google Scholar 

  • Reavey D, Lawton JH (1991) Larval contribution to fitness in leafeating insects. In: Bailey WJ Ridsdill-Smith J (eds), Reproductive behaviour of insects. Champan and Hall, London, pp 293–329

    Google Scholar 

  • Rice JA, Miller TJ, Rose KA, Crowder LB, Marschall EA, Trebitz AS, Deangelis DL (1993) Growth rate variation and larval survival-inferences from an individual-based size-dependent predation model. Can J Fish Aq Sci 50:133–142

    Google Scholar 

  • Ricklefs RE (1969) Preliminary models for growth rates in birds. Ecology 50:1031–1039

    Google Scholar 

  • Ricklefs RE (1973) Patterns of growth in birds. II. Growth rate and mode of development. Ibis 115:177–210

    Google Scholar 

  • Roff DA (1980) Optimizing development time in a seasonal environment: the “ups and downs” of clinal variation. Oecologia 45:202–208

    Google Scholar 

  • Roff DA (1983) Phenological adaptation in a seasonal environment: A theoretical perspective. In: Brown VK, Hodek I (eds) Diapause and life cycle strategies in insects, Junk, The Hague pp 253–270

    Google Scholar 

  • Sibly RM, Calow P (1986) Physiological ecology of animals: an evolutionary approach. Blackwell Scientific Oxford.

    Google Scholar 

  • Sinervo B (1990) Evolution of thermal physiology and growth rate between populations of the western fence lizard (Sceloporus occidentalis). Oecologia 83:228–237

    Google Scholar 

  • Singer MC (1982) Sexual selection for small size in male butterflies. Am Nat 119:337–365

    Google Scholar 

  • Skelly DK, Werner EE (1990) Behavioral and life-historical responses of larval American toads to an odonate predator. Ecology 71:2313–2322

    Google Scholar 

  • Stearns SC (1989) Trade-offs in life-history evolution. Funct Ecol 3:259–268

    Google Scholar 

  • Stearns SC (1992) The evolution of life histories (1st edn). Oxford University Press, Oxford

    Google Scholar 

  • Stearns SC, Koella JC (1986) The evolution of phenotypic plasticity in life-history traits: predictions of reaction norms for age and size at maturity. Evolution 40:893–913

    Google Scholar 

  • Werner EE (1986) Amphibian metamorphosis: growth rates, predation risk and the optimal size at transformation. Am Nat 128:319–341

    Google Scholar 

  • Werner EE, Anholt BR (1993) Ecological consequences of the trade-off between growth and mortality rates mediated by foraging activity. Am Nat 142:242–272

    Google Scholar 

  • Wiklund C, Fagerström T (1977) Why do males emerge before females? A hypothesis to explain the incidence of protandry in butterflies. Oecologia 31:153–158

    Google Scholar 

  • Wiklund C, Persson A, Wickman P-O (1983) Larval aestivation and direct development as alternative strategies in the speckled wood butterfly,Pararge aegeria, in Sweden. Ecol Entomol 8: 233–238

    Google Scholar 

  • Wiklund C, Nylin S, Forsberg J (1991) Sex-related variation in growth rate as a result of selection for large size an protandry in a bivoltine butterfly, Pieris napi. Oikos 60:241–250

    Google Scholar 

  • Wilbur HM (1987) Regulation of structure in complex systems; experimental temporary pond communities. Ecology 68: 1437–1452

    Google Scholar 

  • Wilkinson L, Hill M, Miceli S, Howe P, Vang E (1992) SYSTAT 5.2 Systat, Evanston, Illinois.

    Google Scholar 

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Gotthard, K., Nylin, S. & Wiklund, C. Adaptive variation in growth rate: life history costs and consequences in the speckled wood butterfly,Pararge aegeria . Oecologia 99, 281–289 (1994). https://doi.org/10.1007/BF00627740

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