Abstract

Mate preferences may target traits (a) enhancing offspring adaptation and (b) reducing heterospecific matings. Because similar selective pressures are acting on traits shared by different sympatric species, preference-enhancing offspring adaptation may increase heterospecific mating, in sharp contrast with the classical case of so-called "magic traits." Using a mathematical model, we study which and how many traits will be used during mate choice, when preferences for locally adapted traits increase heterospecific mating. In particular, we study the evolution of preference toward an adaptive versus a neutral trait in sympatric species. We take into account sensory trade-offs, which may limit the emergence of preference for several traits. Our model highlights that the evolution of preference toward adaptive versus neutral traits depends on the selective regimes acting on traits but also on heterospecific interactions. When the costs of heterospecific interactions are high, mate preference is likely to target neutral traits that become a reliable cue limiting heterospecific matings. We show that the evolution of preference toward a neutral trait benefits from a positive feedback loop: The more preference targets the neutral trait, the more it becomes a reliable cue for species recognition. We then reveal the key role of sensory trade-offs and the cost of choosiness favoring the evolution of preferences targeting adaptive traits, rather than traits reducing heterospecific mating. When sensory trade-offs and the cost of choosiness are low, we also show that preferences targeting multiple traits evolve, improving offspring fitness by both transmitting adapted alleles and reducing heterospecific mating. Altogether, our model aims at reconciling "good gene" and reinforcement models to provide general predictions on the evolution of mate preferences within natural communities.

Full Text
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