No abstract

Natural selection has been shown to drive population differentiation and speciation. The role of sexual selection in this process is controversial; however, most of the work has centered on mate choice while the role of male–male competition in speciation is relatively understudied. Here, we outline how male–male competition can be a source of diversifying selection on male competitive phenotypes, and how this can contribute to the evolution of reproductive isolation. We highlight how negative frequency-dependent selection (advantage of rare phenotype arising from stronger male–male competition between similar male phenotypes compared with dissimilar male phenotypes) and disruptive selection (advantage of extreme phenotypes) drives the evolution of diversity in competitive traits such as weapon size, nuptial coloration, or aggressiveness. We underscore that male–male competition interacts with other life-history functions and that variable male competitive phenotypes may represent alternative adaptive options. In addition to competition for mates, aggressive interference competition for ecological resources can exert selection on competitor signals. We call for a better integration of male–male competition with ecological interference competition since both can influence the process of speciation via comparable but distinct mechanisms. Altogether, we present a more comprehensive framework for studying the role of male–male competition in speciation, and emphasize the need for better integration of insights gained from other fields studying the evolutionary, behavioral, and physiological consequences of agonistic interactions.

Investment in reproduction and postzygotic parental care is an energetically costly yet fundamental aspect of the life-history strategies in many species. Recently, oxidative stress has received attention as a potential mediator in the trade-off between reproduction, growth, and survival. During activities that increase metabolic activity, such as providing offspring care, an overproduction of reactive oxygen species can occur that cannot be counteracted by antioxidants, leading to oxidative stress and tissue damage. Here, we investigated the oxidative costs of reproduction and maternal care over the course of the reproductive cycle in a mouthbrooding cichlid fish within socially stable and unstable environments. We manipulated social stability by disrupting the habitat in socially unstable tanks. We expected to see an increase in the burden of maternal care within unstable environments due to increased male harassment of females as a byproduct of increased male–male aggression. We found that brooding females have higher levels of oxidative stress than nonbrooding females and oxidative stress fluctuates throughout the reproductive cycle. These fluctuations were driven by a spike in reactive oxygen metabolites at the beginning of brood care followed by an increase in antioxidant defense. Surprisingly, the link between reproduction and oxidative stress was not different between females from stable or unstable environments. Our study illustrates a more complete picture of the physiological costs of reproduction and parental care throughout different stages of care rather than a simplistic end-point observation of how reproduction and parental care affect an individual.

In many animal societies, dominant individuals have priority access to resources. However, defending high rank can be costly, especially in unstable social hierarchies where there is more intense competition. Oxidative stress has been proposed as a potential cost of social dominance, but few studies have examined this cost in relation to social stability. We studied the cost of social dominance in the cichlid fish Astatotilapia burtoni by manipulating social stability among males in replicate naturalistic communities for 22 weeks. We found that our social stability treatment influenced status-specific patterns in 3 out of 6 measurements of oxidative stress. Specifically, dominant males experienced increased plasma oxidative damage (measured as reactive oxygen metabolites, ROM) compared to subordinate males in stable hierarchies only. Subordinate males in unstable hierarchies had higher ROM than their stable community counterparts, but we found no effect of social stability treatment for dominant males. However, dominant males tended to have lower liver total antioxidant capacity (TAC) than subordinate males in unstable hierarchies, suggesting that the cost of social dominance is higher in unstable hierarchies. There was no other effect of status in tissue (liver, gonad, muscle) or various redox markers including TAC and oxidative DNA damage. We conclude that the stability of the social environment influences the relative cost of social dominance in a tissue and marker specific manner.