Abstract

Body size is a key functional trait that is predicted to decline under warming. Warming is known to cause size declines via phenotypic plasticity, but evolutionary responses of body size to warming are poorly understood. To test for warming-induced evolutionary responses of body size and growth rates, we used populations of mosquitofish (Gambusia affinis) recently established (less than 100 years) from a common source across a strong thermal gradient (19–33°C) created by geothermal springs. Each spring is remarkably stable in temperature and is virtually closed to gene flow from other thermal environments. Field surveys show that with increasing site temperature, body size distributions become smaller and the reproductive advantage of larger body size decreases. After common rearing to reveal recently evolved trait differences, warmer-source populations expressed slowed juvenile growth rates and increased reproductive effort at small sizes. These results are consistent with an adaptive basis of the plastic temperature–size rule, and they suggest that temperature itself can drive the evolution of countergradient variation in growth rates. The rapid evolution of reduced juvenile growth rates and greater reproduction at a small size should contribute to substantial body downsizing in populations, with implications for population dynamics and for ecosystems in a warming world.

Highlights

  • Body size is a key functional trait, dictating energy demand, prey preferences, and the overall ecological role of animals [1,2,3,4,5,6]

  • We used recently established populations of mosquitofish (Gambusia affinis) across a unique geothermal temperature gradient from 19–33°C to test for effects of temperature on the recent evolution of size-related traits

  • Warmer-source populations showed a weaker increase in GSI and fecundity with increasing body size compared to cooler-source populations

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Summary

Introduction

Body size is a key functional trait, dictating energy demand, prey preferences, and the overall ecological role of animals [1,2,3,4,5,6]. If oxygen or resource limitation increases mortality rates for large size individuals, life-history theory predicts the evolution of earlier and greater reproduction at a smaller size [36]. If oxygen or resource limitation stresses large size individuals, reducing the fecundity advantage of large size, life-history theory predicts the evolution of earlier and greater reproduction at a smaller size [36,37]. We sought to test the hypothesis that increased temperature disfavours large body size, causing the rapid evolution of reduced somatic growth rates and a shift in allocation towards greater reproduction at a smaller body size. Using first laboratory generation (F1) adult females reared in a common environment, we tested the prediction that warmer-source populations have recently evolved an increase in reproductive effort at small sizes. We expected growth rates to increase with rearing temperature due to plasticity alone, so this pattern of evolution opposing plasticity would demonstrate the recent evolution of countergradient variation in growth

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