Fitzpatrick, L. J. | bioRxiv Science

bioRxiv2026

Thermally driven sex reversal reveals divergent sex determination dynamics in wild viviparous reptile populations

Climate change can threaten population viability by disrupting sex ratios in species whose sex is influenced by temperature. While species with sex chromosomes were historically considered immune, in some species, temperatures can override genetic sex determination via sex reversal, leaving them vulnerable to climate-driven sex ratio shifts. The Tasmanian spotted snow skink (Carinacincus ocellatus), a viviparous reptile with an XX/XY system, provides a compelling case study. While laboratory studies demonstrated that extreme thermal conditions induce female-to-male sex reversal (XX males), its occurrence in the wild remains unexplored, limiting our understanding of actual climate impacts. Integrating 23 years of phenotypic and genetic sexing data across two climatically distinct populations, we provide the first evidence of sex reversal in a wild viviparous reptile. XX reversal occurred in both populations, affecting up to 23.5% of XX births in the warmer population, and was associated with colder minimum daily temperatures. Despite high birth rates in some years, sex-reversed adults were rare. We also identified putative XY females, suggesting bidirectional sex reversal and reinforcing the extreme plasticity of reptilian sex determination. Ultimately, sex reversal could act as an evolutionary trap, potentially compromising population viability as climate instability increases.

evolutionary biology↗

bioRxiv2022

Population divergence in maternal investment and embryo energy use and allocation reveals adaptive responses to cool climates

The thermal sensitivity of early life stages can play a fundamental role in constraining species distribution. For egg-laying ectotherms, cool temperatures often extend development time and exacerbate developmental energy cost. Despite these costs, egg laying is still observed at high latitudes and altitudes. How embryos overcome the developmental constraints posed by cool climates is crucial knowledge for explaining the persistence of oviparous species in such environments and for understanding thermal adaptation more broadly. Here, we studied maternal investment, and embryo energy use and allocation in wall lizards spanning altitudinal regions, as potential mechanisms of local adaptation to development in cool climates. Specifically, we compared population-level differences in (1) investment from mothers (egg mass, embryo retention and thyroid yolk hormone concentration), (2) embryo energy expenditure during development, and (3) embryo energy allocation from yolk towards tissue. We found evidence that energy expenditure was greater under cool compared with warm incubation temperatures. Females from relatively cool regions did not compensate for this energetic cost of development by producing larger eggs or increasing thyroid hormone concentration in yolk. Instead, embryos from the high-altitude region used less energy to complete development, i.e., they developed faster without a concomitant increase in metabolic rate, compared with those from the low-altitude region. Embryos from high altitudes also allocated relatively more energy towards tissue production, hatching with lower residual yolk:tissue ratios than low-altitude region embryos. These results suggest that local adaptation to cool climate in wall lizards involves mechanisms that regulate embryonic utilisation of yolk reserves and its allocation towards tissue, rather than shifts in maternal investment of yolk content or composition.

evolutionary biology↗