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Sex ratios and bimaturism differ between temperature-dependent and genetic sex-determination systems in reptiles.

ABSTRACT: BACKGROUND:Sex-determining systems may profoundly influence the ecology, behaviour and demography of animals, yet these relationships are poorly understood. Here we investigate whether species with temperature-dependent (TSD) and genetic sex determination (GSD) differ in key demographic traits, using data from 181 species representing all major phylogenetic lineages of extant reptiles. RESULTS:We show that species with TSD exhibit significantly higher within-species variance in sex ratios than GSD species in three major life stages: birth or hatching, juvenility and adulthood. In contrast, sex differences in adult mortality rates do not differ between GSD and TSD species. However, TSD species exhibit significantly greater sex differences in maturation ages than GSD species. CONCLUSION:These results support the recent theoretical model that evolution of TSD is facilitated by sex-specific fitness benefits of developmental temperatures due to bimaturism. Our findings suggest that different sex-determination systems are associated with different demographic characteristics that may influence population viability and social evolution.

SUBMITTER: Bokony V

PROVIDER: S-EPMC6378719 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Sex ratios and bimaturism differ between temperature-dependent and genetic sex-determination systems in reptiles.

Bókony Veronika V Milne Gregory G Pipoly Ivett I Székely Tamás T Liker András A

BMC evolutionary biology 20190218 1

<h4>Background</h4>Sex-determining systems may profoundly influence the ecology, behaviour and demography of animals, yet these relationships are poorly understood. Here we investigate whether species with temperature-dependent (TSD) and genetic sex determination (GSD) differ in key demographic traits, using data from 181 species representing all major phylogenetic lineages of extant reptiles.<h4>Results</h4>We show that species with TSD exhibit significantly higher within-species variance in se ...[more]

PMID: 30777013

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Project description:A common reptile conservation strategy involves artificial incubation of embryos and release of hatchlings or juveniles into wild populations. Temperature-dependent sex determination (TSD) occurs in most chelonians, permitting conservation managers to bias sex ratios towards females by incubating embryos at high temperatures, ultimately allowing the introduction of more egg-bearing individuals into populations. Here, we revisit classic sex allocation theory and hypothesize that TSD evolved in some reptile groups (specifically, chelonians and crocodilians) because male fitness is more sensitive to condition (general health, vigor) than female fitness. It follows that males benefit more than females from incubation environments that confer high-quality phenotypes, and hence high-condition individuals. We predict that female-producing temperatures, which comprise relatively high incubation temperatures in chelonians and crocodilians, are relatively stressful for embryos and subsequent life stages. We synthesize data from 28 studies to investigate how constant temperature incubation affects embryonic mortality in chelonians with TSD. We find several lines of evidence suggesting that warm, female-producing temperatures are more stressful than cool, male-producing temperatures. Further, we find some evidence that pivotal temperatures (TPiv, the temperature that produces a 1:1 sex ratio) may exhibit a correlated evolution with embryonic thermal tolerance. If patterns of temperature-sensitive embryonic mortality are also indicative of chronic thermal stress that occurs post-hatching, then conservation programs may benefit from incubating eggs close to species-specific TPivs, thus avoiding high-temperature incubation. Indeed, our models predict that, on average, a sex ratio of >75% females can generally be achieved by incubating eggs only 1°C above TPiv. Of equal importance, we provide insight into the enigmatic evolution of TSD in chelonians, by providing support to the hypothesis that TSD evolution is related to the quality of the phenotype conferred by incubation temperature, with males produced in high-quality incubation environments.

Dataset Information

Sex ratios and bimaturism differ between temperature-dependent and genetic sex-determination systems in reptiles.

Publications

Sex ratios and bimaturism differ between temperature-dependent and genetic sex-determination systems in reptiles.

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