Sexual differences in physiology are widely regarded as potential proximate mechanisms that underlie sex differences in mortality, life history and disease risk of vertebrates. However, little is known about the causes of sex-specific variation in physiology. Sexual selection and parental workload are two key components suggested to play a role. Theory predicts that, within males, species with stronger male sexual selection (greater sexual dichromatism and more frequent social polygyny) and higher male parental effort should have lower immune capacity and stronger oxidative imbalance. Within females, weak or no direct effect of male sexual selection on physiology is expected, but species where females invest more in parental care should have lower immune capacity and higher oxidative imbalance. We tested these predictions by phylogenetic comparative analyses conducted separately for the two sexes and based on 11,586 physiological measurements of samples collected in the field from 2,048 individuals of 116 and 106 European species for males and females, respectively. For males, we found that the degree of dichromatism, polygyny and male parental effort correlated negatively with multiple immune indices, and the level of antioxidant glutathione correlated positively with polygyny score. In contrast, female immune and oxidative variables were unrelated or weakly related to both male sexual selection or female parental effort. We conclude that sex roles can drive inter-specific variation in immune function (primarily in male birds), but less so in oxidative physiology. These findings support earlier claims that males pay higher physiological costs of sexual selection than females, but apparently also of caregiving. We discuss how females might avoid such costs.

Flight can be highly-energy demanding, but its efficiency depends largely on flight style, wing shape and loading, and a range of morphological and lifestyle adaptations that can modify the cost of sustained flight. Such behavioural and morphological adaptations can also influence the physiological costs associated with migration. For instance, during intense flight and catabolism of reserves, lipid damage induced by pro-oxidants increases, and to keep oxidative physiological homeostasis under control, the antioxidant machinery is upregulated. Studies on the oxidative physiology of endurance flight have produced contradictory results, making generalization difficult, especially because multispecies studies are missing. Therefore, to explore the oxidative cost of flight and migration, we explored the association between three measures of the antioxidant capacity (total antioxidant status, uric acid and glutathione concentration) and one measure of oxidative damage of lipids (malondialdehyde) with variables reflecting flight energetics (year-round or specifically during migration) across 113 European bird species using a phylogenetic framework. We found that none of the traits predicting year-round flight energy expenditure, including flight style, wing morphology and flight muscle morphology explained any measures of oxidative state measured during the energy demanding breeding period, suggesting that birds endure their everyday exercise without or low oxidative cost. However, oxidative damage to lipids and one component of the endogenous antioxidant system (uric acid), measured after the end of spring migration on breeding adult birds, increased with migration distance. Our results suggest that migration might have oxidative consequences that are carried over to subsequent life history stages (breeding).