Oviposition-site choice is a major maternal effect by which females can affect the survival and phenotype of their offspring. Across oviparous species, the ultimate reasons for females' selection of oviposition sites often differ. We present six hypotheses that have been used to explain nonrandom oviposition-site choice in insects, fish, amphibians, reptiles, and birds: (a) maximizing embryo survival, (b) maximizing maternal survival, (c) modifying offspring phenotype, (d) proximity to suitable habitat for offspring, (e) maintaining natal philopatry, and (f) indirect oviposition-site choice via mate choice. Because these hypotheses differ in their relevance across oviparous taxa, each hypothesis must be tested to ensure accurate understanding of the ultimate reason behind oviposition-site choice in a particular taxon. By presenting the major hypotheses for oviposition-site choice as they relate to diverse oviparous animals, we nonetheless illustrate particular trends across animal taxa, while highlighting avenues for future research into the ecological and evolutionary drivers of oviposition-site choice.

Ectothermic animals, such as amphibians and reptiles, are particularly sensitive to rapidly warming global temperatures. One response in these organisms may be to evolve aspects of their thermal physiology. If this response is adaptive and can occur on the appropriate time scale, it may facilitate population or species persistence in the changed environments. However, thermal physiological traits have classically been thought to evolve too slowly to keep pace with environmental change in longer‐lived vertebrates. Even as empirical work of the mid‐20th century offers mixed support for conservatism in thermal physiological traits, the generalization of low evolutionary potential in thermal traits is commonly invoked. Here, we revisit this hypothesis to better understand the mechanisms guiding the timing and patterns of physiological evolution. Characterizing the potential interactions among evolution, plasticity, behavior, and ontogenetic shifts in thermal physiology is critical for accurate prediction of how organisms will respond to our rapidly warming world. Recent work provides evidence that thermal physiological traits are not as evolutionarily rigid as once believed, with many examples of divergence in several aspects of thermal physiology at multiple phylogenetic scales. However, slow rates of evolution are often still observed, particularly at the warm end of the thermal performance curve. Furthermore, the context‐specificity of many responses makes broad generalizations about the potential evolvability of traits tenuous. We outline potential factors and considerations that require closer scrutiny to understand and predict reptile and amphibian evolutionary responses to climate change, particularly regarding the underlying genetic architecture facilitating or limiting thermal evolution.

How are organisms responding to climate change? The rapidity with which climate is changing suggests that, in species with long generation times, adaptive evolution may be too slow to keep pace with climate change, and that alternative mechanisms, such as behavioural plasticity, may be necessary for population persistence. Species with temperature-dependent sex determination may be particularly threatened by climate change, because altered temperatures could skew sex ratios. We experimentally tested nest-site choice in the long-lived turtle Chrysemys picta to determine whether nesting behaviour can compensate for potential skews in sex ratios caused by rapid climate change. We collected females from five populations across the species′ range and housed them in a semi-natural common garden. Under these identical conditions, populations differed in nesting phenology (likely due to nesting frequency), and in nest depth (possibly due to a latitudinal cline in female body size), but did not differ in choice of shade cover over the nest, nest incubation regime, or in resultant nest sex ratios. These results suggest that choice of nest sites with particular shade cover may be a behaviourally plastic mechanism by which turtles can compensate for change in climatic temperatures during embryonic development, provided that sufficient environmental variation in potential nest microhabitat is available. KeywordsChrysemys picta, common garden, geographic variation, painted turtle, phenology, sex ratio Running title: Nest-site choice and climate change Abstract How are organisms responding to climate change? The rapidity with which climate is changing suggests that, in species with long generation times, adaptive evolution may be too slow to keep pace with climate change, and that alternative mechanisms, such as behavioral plasticity, may be necessary for population persistence. Species with temperature-dependent sex determination may be particularly threatened by climate change, because altered temperatures could skew sex ratios. We experimentally investigated nest-site choice in the long-lived turtle Chrysemys picta to determine whether nesting behavior can compensate for potential skews in sex ratios caused by rapid climate change. We collected gravid females from five source populations and housed NOTICE: this is the author's version of a work that was accepted for publication in Biological Conservation. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Biological Conservation, VOL 152, (2012) DOI: 10.1016/j.biocon.2012.03.019 them in a semi-natural common garden. Under these identical conditions, populations differed in nesting phenology due to nesting frequency, and in nest depth due to a latitudinal cline in female body size, but did not differ i...

Maternal ability to match nest characteristics with environmental conditions can influence offspring survival and quality, and may provide a mechanism by which animals can keep pace with climate change. In species with temperaturedependent sex determination that construct subterranean nests, the depth of the nest may affect incubation temperatures, and thus offspring sex ratio. Maternal adjustment of nest depth may be a mechanism by which climate change-induced sex ratio skews could be prevented in globally imperiled taxa such as turtles. We experimentally manipulated nest depth within a biologically relevant range in nests of the model turtle species Chrysemys picta. We then quantified the effects of nest depth on incubation regime, offspring sex ratio and offspring performance. We found no effect of nest depth on six parameters of incubation regime, nor on resultant offspring survival, size or sex ratio. However, deeper nests produced hatchlings that weighed less, and were faster at righting themselves and swimming, than hatchlings from shallower nests. We suggest that cues used by females in adjusting nest depth are unreliable as predictors of future incubation conditions, and the adjustment in nest depth required to affect sex ratio in this species may be too great to keep pace with climate change. Therefore, maternal adjustment of nest depth seems unlikely to compensate for climate change-induced sex ratio skews in small-bodied, freshwater turtles.

The fungal pathogen Batrachochytrium dendrobatidis (Bd) has caused declines and extinctions in amphibians worldwide, and there is increasing evidence that some strains of this pathogen are more virulent than others. While a number of putative virulence factors have been identified, few studies link these factors to specific epizootic events. We documented a dramatic decline in juvenile frogs in a Bd-infected population of Cascades frogs (Rana cascadae) in the mountains of northern California and used a laboratory experiment to show that Bd isolated in the midst of this decline induced higher mortality than Bd isolated from a more stable population of the same species of frog. This highly virulent Bd isolate was more toxic to immune cells and attained higher density in liquid culture than comparable isolates. Genomic analyses revealed that this isolate is nested within the global panzootic lineage and exhibited unusual genomic patterns, including increased copy numbers of many chromosomal segments. This study integrates data from multiple sources to suggest specific phenotypic and genomic characteristics of the pathogen that may be linked to disease-related declines.