The integration of macroevolutionary pattern with developmental mechanism presents an outstanding challenge for studies of phenotypic evolution. Here, we use a combination of experimental and comparative data to test whether evolutionary shifts in the direction of sexual size dimorphism (SSD) correspond to underlying changes in the endocrine regulation of growth. First, we combine captive breeding studies with mark‐recapture data to show that male‐biased SSD develops in the brown anole lizard (Anolis sagrei) because males grow significantly faster than females as juveniles and adults. We then use castration surgeries and testosterone implants to show that castration inhibits, and testosterone stimulates, male growth. We conclude by reviewing published testosterone manipulations in other squamate reptiles in the context of evolutionary patterns in SSD. Collectively, these studies reveal that the evolution of SSD has been accompanied by underlying changes in the effect of testosterone on male growth, potentially facilitating the rapid evolution of SSD.

Survival and reproductive success are determined by the complex interplay between behavior, physiology, morphology, and performance. When optimal trait combinations along these various phenotypic axes differ between sexes or across seasons, regulatory mechanisms such as sex steroids can often facilitate sex-specific and/or seasonal trait expression. In this study, we used surgical castration and replacement of exogenous testosterone in adult male brown anoles (Anolis sagrei) to simultaneously examine the effects of testosterone on a suite of morphological (dewlap area, body size), physiological (immune function), behavioral (dewlap, head bob, and push-up displays), and performance (stamina, sprint speed, bite force) traits. We show that testosterone increases (or castration reduces) growth rate, dewlap area, and bite force. Treatment effects on bite force may simply reflect underlying treatment differences in growth combined with allometry of bite force. Other traits, such as stamina, sprint speed, and rate of behavioral displays, were largely independent of circulating testosterone levels. Although we did not observe significant treatment effects on immune function, we found negative correlations between growth and immune function consistent with the hypothesis that testosterone mediates trade-offs between these competing aspects of energy allocation. Overall, our results demonstrate that testosterone can exert pleiotropic effects on a variety of morphological, physiological, behavioral, and performance traits that are known to influence survival and reproductive success.