Abstract

The evolution of life history is shaped by life expectancy. Life‐history traits coevolve, and optimal states for particular traits are constrained by trade‐offs with other life‐history traits. Life histories contrast among species, but may also diverge intraspecifically, at the level of populations. We studied the evolution of female reproductive allocation strategy, using natural populations of two sympatric species of African annual fishes, Nothobranchius furzeri and Nothobranchius orthonotus. These species inhabit pools in the Mozambican savanna that are formed in the rainy season and persist for only 2–10 months. Using 207 female N. furzeri from 11 populations and 243 female N. orthonotus from 14 populations, we tested the effects of genetic background (intraspecific lineage) and life expectancy (position on the aridity gradient determining maximum duration of their temporary habitat) on female fecundity traits. First, we found that variation in female body mass was small within populations, but varied considerably among populations. Second, we found that fecundity was largely defined by female body mass and that females spawned most of their eggs in the morning. Third, we found that the trade‐off between egg size and egg number varied among lineages of N. furzeri and this outcome has been confirmed by data from two separate years. Overall, we demonstrate that local conditions were important determinants for Nothobranchius growth and fecundity and that eggs size in arid region was less limited by female fecundity than in humid region.

Highlights

  • Life-history traits coevolve due to positive feedbacks and specific constraints, forming complex life-history strategies (Stearns 1992; Roff and Fairbairn 2007)

  • We tested the effect of life expectancy on female life-history traits in natural populations of two sympatric species of annual fish in the genus Nothobranchius

  • 1 We found that female body mass was similar within populations, but varied strongly among populations

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Summary

Introduction

Life-history traits coevolve due to positive feedbacks and specific constraints (trade-offs), forming complex life-history strategies (Stearns 1992; Roff and Fairbairn 2007). The evolution of life history under divergent life expectancy (extrinsic mortality) involves trade-offs between current and future reproduction (Williams 1966; Michod 1979; Kirkwood and Rose 1991). Short life expectancy is predicted to select for rapid maturation (Kirkwood and Rose 1991; Kozłowski 1992). Populations with a short life expectancy are predicted to have small body size and high relative allocation to reproduction early after maturity (Stearns 1992)

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