Geographic variations of life history traits and potential trade-offs in different populations of the parasitoid Leptopilina heterotoma
Abstract
Energy allocation is determined by resource availability and trade-offs among traits, and so organisms have to give some traits priority over others to maximize their fitness according to their environment. In this study, we investigated the geographic variations in life history traits and potential trade-offs in populations of the parasitoid Leptopilina heterotoma (Hymenoptera: Figitidae) originating from the north and the south of the Rhône–Saône valley (over a gradient of 300 km, South-East France). We measured a set of traits related to reproduction, maintenance, and mobility using several estimators of each of these main functions determined at different times. We did not find any clear differences between populations from contrasting areas, whereas the southern populations, which were all assumed to be exposed to similar environmental conditions, displayed contrasting patterns of energy allocation. Thus, the most likely explanation seems to be that the evolution of the life history of L. heterotoma is probably shaped by local selective pressures, such as microclimate, microhabitats, or intensity of competition, rather than by regional ecological conditions. Using our study as an example, we discuss the interest of considering several traits and using different ways of measuring them, concluding that multiple measurements should be performed in future studies to ensure the robustness of the results.
Keywords
Life history traits Trade-off Geographic variations Energy allocation ParasitoidNotes
Acknowledgments
We would like to thank Emmanuel Desouhant and Isabelle Amat for their helpful advice and comments on a previous version of this manuscript. This work is part of the ANR CLIMEVOL project funded by the Agence Nationale de la Recherche. We are also grateful to the Avignon’s center of the Institut National de la Recherche Agronomique and to the landowners who allowed us to collect insects in their orchards.
References
- Addo-bediako A, Chown SL, Gaston KJ (2002) Metabolic cold adaptation in insects: a large-scale perspective. Funct Ecol 16:332–338CrossRefGoogle Scholar
- Allemand R, Fleury F, Lemaitre C, Bouletreau M (1999) Population dynamics and competitive interactions in two species of Leptopilina (Hymenoptera: Figitidae) which parasitize Drosophila in the Rhone Valley (S-E France). Ann Soc Entomol Fr 35:97–103Google Scholar
- Bell G, Koufopanou V (1986) The cost of reproduction. Oxf Surv Evol Biol 3:83–131Google Scholar
- Bezemer T, Harvey J, Mills N (2005) Influence of adult nutrition on the relationship between body size and reproductive parameters in a parasitoid wasp. Ecol Entomol 30:571–580CrossRefGoogle Scholar
- Brown JH, Gillooly JF, Allen AP, Savage VM, West GB (2004) Toward a metabolic theory of ecology. Ecology 85:1771–1789CrossRefGoogle Scholar
- Burton OJ, Phillips BL, Travis JMJ (2010) Trade-offs and the evolution of life-histories during range expansion. Ecol Lett 13:1210–1220PubMedCrossRefGoogle Scholar
- Carroll SP, Hendry AP, Reznick DN, Fox W (2007) Evolution on ecological time-scales. Funct Ecol 21:387–393CrossRefGoogle Scholar
- Carton Y, Boulétreau M, van Alphen JJ, van Lenteren JC (1986) The Drosophila parasitic wasps. In: Ashburner M, Carson HL, Thompson JN (eds) The genetics and biology of Drosophila. Academic, London, pp 347–393Google Scholar
- Clutton-Brock TH, Guinness FE, Albon SD (1982) Red deer: behavior and ecology of two sexes. University of Chicago Press, ChicagoGoogle Scholar
- Crawley MJ (2007) The R book. Wiley, New YorkCrossRefGoogle Scholar
- Eggleton P, Gaston K (1990) Parasitoid species and assemblages—convenient definitions or misleading compromises. Oikos 59:417–421CrossRefGoogle Scholar
- David JR, Clavel MF (1965) Interaction entre le génotype et le milieu d'élevage. Conséquences sur les caractéristiques du développement de la Drosophile. Bul Biol Fr Belg 99:369–378Google Scholar
- Ellers J (1996) Fat and eggs: an alternative method to measure the trade-off between survival and reproduction in insect parasitoids. Neth J Zool 46:227–235CrossRefGoogle Scholar
- Ellers J, van Alphen JJ (1997) Life history evolution in Asobara tabida: plasticity in allocation of fat reserves to survival and reproduction. J Evol Biol 10:771–785CrossRefGoogle Scholar
- Ellers J, Driessen G, Sevenster J (2000) The shape of the trade-off function between egg production and life span in the parasitoid Asobara tabida. Neth J Zool 50:29–36Google Scholar
- Fleury F, Ris N, Allemand R, Fouillet P, Carton Y, Bouletreau M (2004) Ecological and genetic interactions in Drosophila–parasitoids communities: a case study with D. melanogaster, D. simulans and their common Leptopilina parasitoids in south-eastern France. Genetica 120:181–194PubMedCrossRefGoogle Scholar
- Fleury F, Gibert P, Ris N, Allemand R (2009) Ecology and life history evolution of frugivorous Drosophila parasitoids. Adv Parasitol 70:3–44PubMedCrossRefGoogle Scholar
- Fox C, Czesak M (2000) Evolutionary ecology of progeny size in arthropods. Annu Rev Entomol 45:341–369PubMedCrossRefGoogle Scholar
- Gibert P, Allemand R, Henri H, Huey RB (2010) Local adaptation and evolution of parasitoid interactions in an invasive species, Drosophila subobscura. Evol Ecol Res 12:873–883Google Scholar
- Gilchrist GW, Huey RB (2004) Plastic and genetic variation in wing loading as a function of temperature within and among parallel clines in Drosophila subobscura. Integr Comp Biol 44:461–470PubMedCrossRefGoogle Scholar
- Giron D, Casas J (2003) Lipogenesis in an adult parasitic wasp. J Insect Physiol 49:141–147PubMedCrossRefGoogle Scholar
- Giron D, Rivero A, Mandon N, Darrouzet E, Casas J (2002) The physiology of host feeding in parasitic wasps: implications for survival. Funct Ecol 16:750–757CrossRefGoogle Scholar
- Godfray HCJ (1987) The evolution of clutch size in parasitic wasps. Am Nat 129:221–233CrossRefGoogle Scholar
- Godfray HCJ (1994) Parasitoids: behavioral and evolutionary ecology. Princeton University Press, PrincetonGoogle Scholar
- Hairston NG Jr, Ellner SP, Geber MA, Yoshida T, Fox JA (2005) Rapid evolution and the convergence of ecological and evolutionary time. Ecol Lett 8:1114–1127CrossRefGoogle Scholar
- Irlich UM, Terblanche JS, Blackburn TM, Chown SL (2009) Insect rate–temperature relationships: environmental variation and the metabolic theory of ecology. Am Nat 174:819–835PubMedCrossRefGoogle Scholar
- Jervis M, Ellers J, Harvey J (2008) Resource acquisition, allocation, and utilization in parasitoid reproductive strategies. Annu Rev Entomol 53:361–385PubMedCrossRefGoogle Scholar
- Jervis MA, Moe A, Heimpel GE (2012) The evolution of parasitoid fecundity: a paradigm under scrutiny. Ecol Lett 15:357–364CrossRefGoogle Scholar
- de Jong G, van Noordwijk AJ (1992) Acquisition and allocation of resources: genetic (CO) variances, selection, and life histories. Am Nat 139:749–770CrossRefGoogle Scholar
- Nespolo R, Roff D, Fairbairn D (2008) Energetic trade-off between maintenance costs and flight capacity in the sand cricket (Gryllus firmus). Funct Ecol 22:624–631CrossRefGoogle Scholar
- Nur N (1988) The cost of reproduction in birds—an examination of the evidence. Ardea 76:155–168Google Scholar
- Price PW (1974) Strategies for egg production. Evolution 28:76–84CrossRefGoogle Scholar
- Reznick D (1985) Costs of reproduction: an evaluation of the empirical evidence. Oikos 44:257–267CrossRefGoogle Scholar
- Reznick D, Nunney L, Tessier A (2000) Big houses, big cars, superfleas and the costs of reproduction. Trends Ecol Evol 15:421–425PubMedCrossRefGoogle Scholar
- Reznick DN, Ghalambor CK (2001) The population ecology of contemporary adaptations: what empirical studies reveal about the conditions that promote adaptive evolution. Genetica 112–113:183–198PubMedCrossRefGoogle Scholar
- Ris N, Allemand R, Fouillet P, Fleury F (2004) The joint effect of temperature and host species induce complex genotype-by-environment interactions in the larval parasitoid of Drosophila, Leptopilina heterotoma (Hymenoptera: Figitidae). Oikos 106:451–456CrossRefGoogle Scholar
- Roff DA (1992) The evolution of life histories. Chapman and Hall, LondonGoogle Scholar
- Roff DA, Fairbairn DJ (2007) The evolution of trade-offs: where are we? J Evol Biol 20:433–447PubMedCrossRefGoogle Scholar
- Saglam I, Roff D, Fairbairn D (2008) Male sand crickets trade-off flight capability for reproductive potential. J Evol Biol 21:997–1004PubMedCrossRefGoogle Scholar
- Stearns SC (1992) The evolution of life histories. Oxford University Press, OxfordGoogle Scholar
- Steigenga MJ, Zwaan BJ, Brakefield PM, Fischer K (2005) The evolutionary genetics of egg size plasticity in a butterfly. J Evol Biol 18:281–289PubMedCrossRefGoogle Scholar
- Thompson JN (1999) The evolution of species interactions. Nature 284:2116–2118Google Scholar
- Thorpe RS, Reardon JT, Malhotra A (2005) Common garden and natural selection experiments support ecotypic differentiation in the Dominican anole (Anolis oculatus). Am Nat 165:495–504PubMedCrossRefGoogle Scholar
- Vayssade C, Martel V, Moiroux J, Fauvergue X, van Alphen JJM, van Baaren J (2012) The response of life-history traits to a new species in the community: a story with Drosophila parasitoids from the Rhône and Saone valleys. Biol J Linn Soc 107:125–165CrossRefGoogle Scholar
- Van Handel E (1985) Rapid determination of total lipids in mosquitoes. J Am Mosquito Contr 3:302–304Google Scholar
- Visser B, Le Lann C, den Blanken F, Harvey J, van Alphen JJ, Ellers J (2010) Loss of lipid synthesis as an evolutionary consequence of a parasitic lifestyle. Proc Natl Acad Sci 107:8677–8682PubMedCrossRefGoogle Scholar
- Zera AJ, Harshman LG (2001) The physiology of life history trade-offs in animals. Ann Rev Ecol Syst 32:95–126CrossRefGoogle Scholar
- Zera AJ, Larsen A (2001) The metabolic basis of life history variation: genetic and phenotypic differences in lipid reserves among life history morphs of the wing-polymorphic cricket, Gryllus firmus. J Insect Physiol 47:1147–1160PubMedCrossRefGoogle Scholar