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Global climate change has profound effects on species, especially those in habitats already altered by humans. Tropical ectotherms are predicted to be at high risk from global temperature increases, particularly those adapted to cooler temperatures at higher altitudes. We investigated how one such species, the water anole (Anolis aquaticus), is affected by temperature stress similar to that of a warming climate across a gradient of human-altered habitats at high elevation sites. We conducted a field survey on thermal traits and measured lizard critical thermal maxima across the sites. From the field survey, we found that (1) lizards from the least disturbed site and (2) operative temperature models of lizards placed in the least disturbed site had lower temperatures than those from sites with histories of human disturbance. Individuals from the least disturbed site also demonstrated greater tolerance to high temperatures than those from the more disturbed sites, in both their critical thermal maxima and the time spent at high temperatures prior to reaching critical thermal maxima. Our results demonstrate within-species variability in responses to high temperatures, depending on habitat type, and provide insight into how tropical reptiles may fare in a warming world. 

Abstract Background Increases in temperature variability associated with climate change have critical implications for the phenology of wildlife across the globe. For example, warmer winter temperatures can induce forward shifts in breeding phenology across taxa (“false springs”), which can put organisms at risk of freezing conditions during reproduction or vulnerable early life stages. As human activities continue to encroach on natural ecosystems, it is also important to consider how breeding phenology interacts with other anthropogenic stressors (e.g., pollutants). Using 14 populations of a widespread amphibian (wood frog; Rana sylvatica ), we compared 1) growth; 2) tolerance to a common wetland contaminant (NaCl); and 3) the ability of tadpoles to acclimate to lethal NaCl exposure following sublethal exposure earlier in life. We evaluated these metrics across two breeding seasons (2018 and 2019) and across populations of tadpoles whose parents differed in breeding phenology (earlier- versus later-breeding cohorts). In both years, the earlier-breeding cohorts completed breeding activity prior to a winter storm and later-breeding cohorts completed breeding activities after a winter storm. The freezing conditions that later-breeding cohorts were exposed to in 2018 were more severe in both magnitude and duration than those in 2019. Results In 2018, offspring of the later-breeding cohort were larger but less tolerant of NaCl compared to offspring of the earlier-breeding cohort. The offspring of the earlier-breeding cohort additionally were able to acclimate to a lethal concentration of NaCl following sublethal exposure earlier in life, while the later-breeding cohort became less tolerant of NaCl following acclimation. Interestingly, in 2019, the warmer of the two breeding seasons, we did not detect the negative effects of later breeding phenology on responses to NaCl. Conclusions These results suggest that phenological shifts that expose breeding amphibians to freezing conditions can have cascading consequences on offspring mass and ability to tolerate future stressors but likely depends on the severity of the freeze event. 

Threat of predation often requires animals to seek refuge in unusual or suboptimal habitats. While aquatic refugia are thought to be used by many terrestrial animal species, there are challenges associated with aquatic refugia that could preclude their actual usefulness, particularly to air‐breathing ectotherms. Consequently, observations that can shed light on the evolution of antipredator strategies that cross the air–water interface are particularly valuable. “Semi‐aquatic” spiders in the family Trechaleidae have not been documented using diving as part of their antipredator behavior and, indeed, they are rarely known to submerge themselves at all, as their aquatic foraging occurs from a terrestrial location. The lack of diving behavior is hypothesized to be due to the high potential costs (e.g., thermal and respiratory) of submergence. Despite this, we document the prolonged underwater refuge use (>30 min) ofTrechalea extensafollowing pursuit by a perceived threat (humans). We also identify some morphological adaptations that may potentially help counterbalance these costs and permit underwater antipredator behavior, specifically the ability of cuticular hairs to provide a hydrophobic surface, allowing the formation of a plastron that, in turn, may facilitate respiratory function and reduce heat loss. These observations expand our overall understanding of habitat use in this genus and, more generally, antipredator adaptations of spiders.