Abstract

Behavioral isolation is thought to arise early in speciation due to differential sexual and/or natural selection favoring different preferences and traits in different lineages. Instead, behavioral isolation can arise due to reinforcement favoring traits and preferences that prevent maladaptive hybridization. In darters, female preference for male coloration has been hypothesized to drive speciation, because behavioral isolation evolves before F1 inviability. However, as with many long‐lived organisms, the fitness of second‐generation hybrids has not been assessed because raising animals to adulthood in the laboratory is challenging. Of late, reinforcement of male preferences has been implicated in darters because male preference for conspecific females is high in sympatry but absent in allopatry in multiple species pairs. The hypothesis that reinforcement accounts for behavioral isolation in sympatry assumes that hybridization and postzygotic isolation are present. Here, we used genomic and morphological data to demonstrate that hybridization is ongoing between orangethroat and rainbow darters and used hybrids collected from nature to measure postzygotic barriers across two hybrid generations. We observed sex ratio distortion in adult F1s and a dramatic reduction in backcross survival. Our findings indicate that selection to avoid hybridization promotes the evolution of male‐driven behavioral isolation via reinforcement in this system.

Highlights

  • It is recognized that hybridization can promote speciation through reinforcement, the process by which enhanced prezygotic isolation is favored in sympatry in response to postzygotic isolation (Coyne & Orr, 2004; Dobzhansky, 1937; Servedio & Noor, 2003)

  • We found high levels of postzygotic isolation between orangethroat and rainbow darters in the form of multiple isolating barriers spanning across hybrid life stages and generations

  • We used genomic data to demonstrate that hybridization is ongoing between orangethroat and rainbow darters

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Summary

Introduction

The increasing availability of genomic sequence data for nonmodel organisms has revealed that hybridization is surprisingly common between species (Abbott et al, 2013; Mallet, 2005). As hybridization has traditionally been thought of as a homogenizing force, a major question in evolutionary biology is how speciation can proceed in the face of gene flow (Bolnick & Fitzpatrick, 2007; Feder, Egan, & Nosil, 2012; Felsenstein, 1981; Harrison & Larson, 2014). It is recognized that hybridization can promote speciation through reinforcement, the process by which enhanced prezygotic isolation is favored in sympatry in response to postzygotic isolation (Coyne & Orr, 2004; Dobzhansky, 1937; Servedio & Noor, 2003). Reinforcement causes reproductive character displacement (RCD), whereby behavioral isolation between two species is heightened in sympatry compared to allopatry. Multiple different evolutionary forces can lead to such a pattern (reviewed in Hoskin & Higgie, 2010), it is considered reinforcement when the mechanism underlying RCD is selection against hybridization (Pfennig & Pfennig, 2012). Empirical and theoretical research has indicated that reinforcement may be more common than previously thought (Hudson & Price, 2014; Yukilevich, 2012)

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