Theoretical models suggest that in changing environments natural selection on two traits, maternal nesting behaviour and pivotal temperatures (those that divide the sexes) is important for maintaining viable offspring sex ratios in species with environmental sex determination (ESD). Empirical evidence, however, is lacking. In this paper, we provide such evidence from a study of clinal variation in four sex-determining traits (maternal nesting behaviour, pivotal temperatures, nesting phenology, and nest depth) in Physignathus lesueurii, a wide-ranging ESD lizard inhabiting eastern Australia. Despite marked differences in air and soil temperatures across our five study sites spanning 19°latitude and 1200 m in elevation, nest temperatures did not differ significantly among sites. Lizards compensated for climatic differences chiefly by selecting more open nest sites with higher incident radiation at cooler sites. Clinal variation in the onset of nesting also compensated for climatic differences, but to a lesser extent. There was no evidence of compensation through pivotal temperatures or nest depth. More broadly, our results extend to the egg stage the life history prediction that behaviour is the chief compensatory mechanism for climatic differences experienced by species spanning environmental extremes. Furthermore, our study was unique in revealing that nest site choice influenced mainly the daily range in nest temperatures, rather than mean temperatures, in a shallow-nesting reptile. Finally, indirect evidence suggests that the cue used by nesting lizards was radiation or temperature (through basking or assessing substrate temperatures), not visual detection of canopy openness. We conclude that maternal nesting behaviour and nesting phenology are traits subject to sex ratio selection in P. lesueurii, and thus, must be considered among the repertoire of ESD species for responding to climate change.
The cane toad Bufo marinus has been migrating westward across northern Australia since its introduction as a biological control agent in 1935. It has been implicated in the widespread decline of many native frog-eating predators. To investigate the impacts of this invasive species on native predatory reptiles, annual surveys were conducted from 2001 to 2007 to document variation in the relative abundances of three varanid lizards (Varanus mertensi, Varanus mitchelli and Varanus panoptes) and one crocodile Crocodylus johnstoni species known to consume toads. In addition, the indirect effects of this variation on one agamid lizard Amphibolurus gilberti, a known prey item of V. panoptes, were also examined. Surveys were performed at two sites in northern Australia before and after the arrival of B. marinus. Significant declines in the relative abundances of all three species of varanid lizard were observed following toad arrival. Declines in the abundance of V. panoptes, V. mitchelli and V. mertensi at the two sites ranged 83-96, 71-97 and 87-93%, respectively. In contrast, A. gilberti increased by 23-26%; whereas there were no significant population-level declines in C. johnstoni despite observations of individual effects (i.e. several dead crocodiles with B. marinus in their stomachs). These findings suggest population-level changes in Australian lizards caused by an invasive species.
An increase in temperature, within bounds, will accelerate development of reptile embryos, and morphogenesis can be normal over a range of temperatures despite those varying rates of development. Less well understood is the form of the relationship that best describes variation in developmental rate with temperature. In this article, we apply a linear degree.hour model, an empirical curvilinear model, a biophysical model, and a polynomial model to data on rates of embryonic development and temperature in the pig-nosed turtle Carettochelys insculpta from northern Australia. The curvilinear models, which have been applied with success to development of insects, describe the embryonic development of turtles well. When fluctuating temperatures extend beyond the constant temperatures that support successful incubation, the curvilinear models continue to perform well, whereas the linear model predictions fail. Sensitivity analysis indicates that under some circumstances, incubation duration may be increased by diel temperature fluctuations, independent of an influence of mean temperature. In other circumstances, incubation duration may be decreased, and in still other circumstances, diel temperature fluctuations will have no impact on incubation duration. This adds an additional dimension to our understanding of how thermal regimes can be selected or manipulated by reptiles to optimise incubation duration and the timing of offspring emergence.
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