Gestation periods vary greatly across elasmobranch species. Differences in body size and body temperature (i.e. major determinants of metabolic rates) might explain such variation. Although temperature effects have been demonstrated for captive animals, body size effects remain undocumented. Moreover, whether metabolic rates of mothers or those of embryos affect gestation periods remains unclear. Because biological times generally scale with mass1−β, where β is metabolic scaling exponent (0.8–0.9 in fishes), we hypothesized that elasmobranch gestation periods would scale with mass0.1–0.2. We also hypothesized that regionally endothermic species with elevated metabolic rates should have shorter gestation periods than similar-sized ectothermic species if the metabolic rates of mothers are responsible. We compiled data on gestation periods for 36 elasmobranch species to show that gestation periods scale with M0.11 and m0.17, where M and m are adult female mass and birth mass, respectively. Litter size and body temperature also affected gestation periods. Our findings suggest that the body-mass dependence of metabolic rate explains some variations in elasmobranch gestation periods. Unexpectedly, regionally endothermic sharks did not have shorter gestation periods than their ectothermic counterparts, suggesting that the metabolic rates of embryos, which are likely ectothermic in all elasmobranch species, may be responsible. This article has an associated First Person interview with the first author of the paper.

Sex change is a well‐known phenomenon in teleost fishes, and it takes several days to a few months depending on the species and direction of sex change. However, the underlying factors influencing the time required for sex change (TS) remain unclear. Given that the time for producing a new gonad largely determines TS, the gonad type (i.e., whether fish retain the gonad of opposite sex or not [delimited or non‐delimited]) and metabolic rate may affect TS. This study sought to test two hypotheses: (1) the delimited gonad shortens TS and (2) TS scales with mass0.1−0.2, because the metabolic scaling exponent (β) in fishes is 0.8–0.9 and biological times scale with mass1−β in general. We compiled data on TS for 12 female‐to‐male and 14 male‐to‐female sex‐changing species from the literature. Results of individual examinations of the effects of gonad type and mass were consistent with our hypotheses. However, upon simultaneous examination of the effects of gonad type and mass, these effects became unclear because of their strong multicollinearity. The compiled data for delimited and non‐delimited gonads were biased toward the smaller and larger species, respectively, precluding us from being able to statistically distinguish between these effects. Small species with non‐delimited gonads and large species with delimited gonads exist; however, their TS has not been measured with high temporal resolution thus far. Therefore, additional experiments on these species are required to statistically distinguish between, as well as to better understand, the effects of gonad type and mass on TS.