Abstract

Assortative mating promotes reproductive isolation and allows allopatric speciation processes to continue in secondary contact. As mating patterns are determined by mate preferences and intrasexual competition, we investigated male–male competition and behavioral isolation in simulated secondary contact among allopatric populations. Three allopatric color morphs of the cichlid fish Tropheus were tested against each other. Dyadic male–male contests revealed dominance of red males over bluish and yellow-blotch males. Reproductive isolation in the presence of male–male competition was assessed from genetic parentage in experimental ponds and was highly asymmetric among pairs of color morphs. Red females mated only with red males, whereas the other females performed variable degrees of heteromorphic mating. Discrepancies between mating patterns in ponds and female preferences in a competition-free, two-way choice paradigm suggested that the dominance of red males interfered with positive assortative mating of females of the subordinate morphs and provoked asymmetric hybridization. Between the nonred morphs, a significant excess of negative assortative mating by yellow-blotch females with bluish males did not coincide with asymmetric dominance among males. Hence, both negative assortative mating preferences and interference of male–male competition with positive assortative preferences forestall premating isolation, the latter especially in environments unsupportive of competition-driven spatial segregation.

Highlights

  • Speciation depends on the reduction of gene flow between diverging taxa

  • As mating patterns are determined by mate preferences and intrasexual competition, we investigated male–male competition and behavioral isolation in simulated secondary contact among allopatric populations

  • Ecology and Evolution published by John Wiley & Sons Ltd

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Summary

Introduction

Speciation depends on the reduction of gene flow between diverging taxa. Reproductive isolation is readily initiated by physical barriers, before, eventually, intrinsic barriers to gene flow complete speciation (Coyne and Orr 2004). Mate preferences have been shown to have a genetic basis in many animals (reviewed by Bakker and Pomiankowski 1995; within species: Jennions and Petrie 1997; among species: Laturney and Moehring 2012), and there is a growing evidence for the importance of sexual imprinting during early development. In most natural rearing environments, young animals are likely to imprint on conspecific signals, and learnt preferences may sustain sexual isolation between closely related a 2015 The Authors.

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