Abstract

Despite decades of research, empirical support for the ‘compatible genes’ and ‘good genes’ hypotheses as explanations for adaptive female extra-pair mating remains discordant. One largely un-tested theoretical prediction that could explain equivocal findings is that mating for compatible genes benefits should reduce selection for good genes. However, this prediction does not consider demographic parameters, such as social structuring, that can indirectly influence extra-pair paternity (EPP) outcomes. Drawing on evidence from a previous study, we re-evaluate this hypothesis whilst considering social structuring in a population of tui, Prosthemadera novaeseelandiae, a socially monogamous passerine. Previous research has found possible evidence for mating for good genes because male ornament size correlates with EPP success in this population. Here, we test whether non-random inbreeding of social-pairs indirectly provides the opportunity to gain compatibility benefits from EPP, and thus whether selection for compatible genes and good genes can operate simultaneously. We found that 1) social mates were more closely related than expected through random mating, 2) extra-pair males were less closely related to females than were the females’ within-pair mates, and 3) genetically dissimilar males sired offspring with faster growth rates. These results demonstrate that females gain compatible genes benefits from EPP. However, contrary to the compatible genes hypothesis, females in highly-related pairs did not engage more frequently in extra-pair mating. Together with previous research investigating female mate choice in this population, our findings suggest that social pairings between relatives provide a pathway for females to gain compatible genes benefits whilst engaging in extra-pair mating for good genes. This study provides evidence that some fitness benefits from EPP arise automatically through non-random social mating rather than through direct selection on extra-pair mate choice. We argue that when variance in compatibility benefits is an outcome of population structuring, compatible genes benefits need not be gained at the expense of good genes benefits.

Highlights

  • The adaptive function of female multiple mating in socially monogamous species has been variously debated over the past few decades (Westneat et al, 1990; Birkhead and Møller, 1992; Westneat and Stewart, 2003), so far no obvious conclusion has been reached (Wan et al, 2013)

  • Because growth rates are an important component of offspring performance (Lindstrom, 1999) that are associated with non-additive genetic quality (Keller and Waller, 2002; Kempenaers, 2007; Pitcher and Neff, 2007; Dziminski et al, 2008; Rosivall et al, 2009), we examine the effect of genetic relatedness of biological parents on offspring growth rates, and compare within-pair and extrapair maternal half-siblings to determine whether genetically dissimilar males provide compatibility benefits to females

  • We examined the probability of male-female pairs from the same area being a social pair using a generalized linear mixed-effects model (GLMM) with a logit link function and binomial error distribution

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Summary

Introduction

The adaptive function of female multiple mating in socially monogamous species has been variously debated over the past few decades (Westneat et al, 1990; Birkhead and Møller, 1992; Westneat and Stewart, 2003), so far no obvious conclusion has been reached (Wan et al, 2013). Under the compatible genes hypothesis, not all females stand to derive the same benefits from mating with a particular male (Neff and Pitcher, 2005; Puurtinen et al, 2009) Instead, it is the compatibility of male and female genotypes that act, through either heterozygote overdominance or avoidance of the deleterious effects of inbreeding, to produce genetically superior offspring (Zeh and Zeh, 1996, 1997; Jennions, 1997; Tregenza and Wedell, 2000). Inbreeding depression is a consequence of intragenomic conflict caused by increased shared genetic similarity by common descent and lowered functional genome-wide heterozygosity (Coulson et al, 1998) These genetic consequences have the potential to influence fitness through their detrimental effects on offspring birth weights, growth, and survival (Keller and Waller, 2002). The compatible genes hypothesis predicts that paternity should be biased toward genetically dissimilar males

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