Population genetic theory predicts that adaptation in novel environments is enhanced by genetic variation for fitness. However, theory also predicts that under strong selection, demographic stochasticity can drive populations to extinction before they can adapt. We exposed wheat-adapted populations of the flour beetle (Tribolium castaneum) to a novel suboptimal corn resource, to test the effects of founding genetic variation on population decline and subsequent extinction or adaptation. As previously Classical population genetic theory predicts that the amount of additive genetic variation for fitness in a population increases the response to directional selection (Fisher 1930). More recent theoretical work suggests, however, that the interaction between genetic variation and fitness is more complex. For instance, the effect of genetic variance in a fitness-relevant trait is also determined by environmental fluctuations, which can inflict a genetic load due to changing phenotypic optima (Lande and Shannon 1996). Another genetic constraint is imposed by the genetic covariance structure, which determines the effect of selection acting simultaneously on multiple traits (Blows and Hoffmann 2005). Additionally, demographic constraints can determine the importance of genetic variation during adaptation. For instance, under

Many predators and parasites eavesdrop on the communication signals of their prey. Eavesdropping is typically studied as dyadic predator-prey species interactions; yet in nature, most predators target multiple prey species and most prey must evade multiple predator species. The impact of predator communities on prey signal evolution is not well understood. Predators could converge in their preferences for conspicuous signal properties, generating competition among predators and natural selection on particular prey signal features. Alternatively, predator species could vary in their preferences for prey signal properties, resulting in sensory-based niche partitioning of prey resources. In the Neotropics, many substrate-gleaning bats use the mate-attraction songs of male katydids to locate them as prey. We studied mechanisms of niche partitioning in four substrate-gleaning bat species and found they are similar in morphology, echolocation signal design and prey-handling ability, but each species preferred different acoustic features of male song in 12 sympatric katydid species. This divergence in predator preference probably contributes to the coexistence of many substrate-gleaning bat species in the Neotropics, and the substantial diversity in the mate-attraction signals of katydids. Our results provide insight into how multiple eavesdropping predator species might influence prey signal evolution through sensory-based niche partitioning.

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