Sex-determining mechanisms are broadly categorised as being based on either genetic or environmental factors. Vertebrate sex determination exhibits remarkable diversity but displays distinct phylogenetic patterns. While all eutherian mammals possess XY male heterogamety and female heterogamety (ZW) is ubiquitous in birds, poikilothermic vertebrates (fish, amphibians and reptiles) exhibit multiple genetic sex-determination (GSD) systems as well as environmental sex determination (ESD). Temperature is the factor controlling ESD in reptiles and temperature-dependent sex determination (TSD) in reptiles has become a focal point in the study of this phenomenon. Current patterns of climate change may cause detrimental skews in the population sex ratios of reptiles exhibiting TSD. Understanding the patterns of variation, both within and among populations and linking such patterns with the selection processes they are associated with, is the central challenge of research aimed at predicting the capacity of populations to adapt to novel conditions. Here we present a conceptual model that innovates by defining an individual reaction norm for sex determination as a range of incubation temperatures. By deconstructing individual reaction norms for TSD and revealing their underlying interacting elements, we offer a conceptual solution that explains how variation among individual reaction norms can be inferred from the pattern of population reaction norms. The model also links environmental variation with the different patterns of TSD and describes the processes from which they may arise. Specific climate scenarios are singled out as eco-evolutionary traps that may lead to demographic extinction or a transition to either male or female heterogametic GSD. We describe how the conceptual principles can be applied to interpret TSD data and to explain the adaptive capacity of TSD to climate change as well as its limits and the potential applications for conservation and management programs.
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Univ Paris Saclay, CNRS, AgroParisTech, Ecol Systemat & Evolut, F-91190 Gif Sur Yvette, FranceUniv Paris Saclay, CNRS, AgroParisTech, Ecol Systemat & Evolut, F-91190 Gif Sur Yvette, France
Monsinjon, Jonathan R.
Guillon, Jean-Michel
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Univ Paris Saclay, CNRS, AgroParisTech, Ecol Systemat & Evolut, F-91190 Gif Sur Yvette, FranceUniv Paris Saclay, CNRS, AgroParisTech, Ecol Systemat & Evolut, F-91190 Gif Sur Yvette, France
Guillon, Jean-Michel
Wyneken, Jeanette
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Florida Atlantic Univ, Dept Biol Sci, Boca Raton, FL USAUniv Paris Saclay, CNRS, AgroParisTech, Ecol Systemat & Evolut, F-91190 Gif Sur Yvette, France
Wyneken, Jeanette
Girondot, Marc
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Univ Paris Saclay, CNRS, AgroParisTech, Ecol Systemat & Evolut, F-91190 Gif Sur Yvette, France
Univ Paris Saclay, Ecol, Systemat, Evolut,AgroParisTech, F-91190 Gif Sur Yvette, FranceUniv Paris Saclay, CNRS, AgroParisTech, Ecol Systemat & Evolut, F-91190 Gif Sur Yvette, France
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Iowa State Univ, Dept Ecol Evolut & Organism Biol, Ames, IA 50011 USA
Duke Univ, Dept Biol, Durham, NC USAIowa State Univ, Dept Ecol Evolut & Organism Biol, Ames, IA 50011 USA
McGaugh, Suzanne E.
Bowden, Rachel M.
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Iowa State Univ, Dept Ecol Evolut & Organism Biol, Ames, IA 50011 USA
Illinois State Univ, Sch Biol Sci, Normal, IL 61761 USAIowa State Univ, Dept Ecol Evolut & Organism Biol, Ames, IA 50011 USA
Bowden, Rachel M.
Kuo, Chin-Horng
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Iowa State Univ, Dept Ecol Evolut & Organism Biol, Ames, IA 50011 USA
Acad Sinica, Inst Plant & Microbial Biol, Taipei 115, TaiwanIowa State Univ, Dept Ecol Evolut & Organism Biol, Ames, IA 50011 USA
Kuo, Chin-Horng
Janzen, Fredric J.
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Iowa State Univ, Dept Ecol Evolut & Organism Biol, Ames, IA 50011 USAIowa State Univ, Dept Ecol Evolut & Organism Biol, Ames, IA 50011 USA