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
Clutton-Brock TH, Albon SD, Guinness FE (1985) Parental investment and sex differences in juvenile mortality in birds and mammals. Nature 313:131–133
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
Crowl TA, Covich AP (1990) Predator-induced life-history shifts in a freshwater snail. Science 247:949–951
Fraser DF, Gilliam JF (1992) Nonlethal impacts of predator invasion: facultative suppression of growth and reproduction. Ecology 73:959–970
Gebhardt MD, Stearns SC (1988) Reaction norms for development time and weight at eclosion inDrosophila mercatorum. J Evol Biol 1:335–354
Gunnarsson B, Johnsson J (1990) Protandry and moulting in the spider Pityohyphantes phrygianus. Oikos 59:205–212
Higgins LG (1977) The speckled wood (Pararge aegeria L.) in Madeira. Entomol Rec J Var 89:22–23
Higgins LG, Hargreaves B (1983) The butterflies of Britain and Europe. Collins, London
Lima S, Dill LM (1990) Behavioral descision made under the risk of predation: a reveiw and prospectus. Can J Zool 68:619–640
Negus NC, Berger PJ (1992) Phenotypic plasticity of the montane vole (Microtus montanus) in unpredictable environments. Can J Zool 70:2121–2124
Niewiarowski PH, Roosenburg W (1993) Reciprocal transplant reveals sources of variation in growth rates of the lizardSceloporus undulatus. Ecology 74:1992–2002
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
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
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
Perrin N, Rubin JF (1990) On dome-shaped norms of reaction for size-to-age at maturity in fishes. Funct Ecol 4 53–57
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
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
Ricklefs RE (1969) Preliminary models for growth rates in birds. Ecology 50:1031–1039
Ricklefs RE (1973) Patterns of growth in birds. II. Growth rate and mode of development. Ibis 115:177–210
Roff DA (1980) Optimizing development time in a seasonal environment: the “ups and downs” of clinal variation. Oecologia 45:202–208
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
Sibly RM, Calow P (1986) Physiological ecology of animals: an evolutionary approach. Blackwell Scientific Oxford.
Sinervo B (1990) Evolution of thermal physiology and growth rate between populations of the western fence lizard (Sceloporus occidentalis). Oecologia 83:228–237
Singer MC (1982) Sexual selection for small size in male butterflies. Am Nat 119:337–365
Skelly DK, Werner EE (1990) Behavioral and life-historical responses of larval American toads to an odonate predator. Ecology 71:2313–2322
Stearns SC (1989) Trade-offs in life-history evolution. Funct Ecol 3:259–268
Stearns SC (1992) The evolution of life histories (1st edn). Oxford University Press, Oxford
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
Werner EE (1986) Amphibian metamorphosis: growth rates, predation risk and the optimal size at transformation. Am Nat 128:319–341
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
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
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
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
Wilbur HM (1987) Regulation of structure in complex systems; experimental temporary pond communities. Ecology 68: 1437–1452
Wilkinson L, Hill M, Miceli S, Howe P, Vang E (1992) SYSTAT 5.2 Systat, Evanston, Illinois.
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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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DOI: https://doi.org/10.1007/BF00627740