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Climate change is generating range shifts in many organisms, notably along the altitudinal gradient. However, moving up in altitude exposes organisms to lower oxygen availability, which may negatively affect development and fitness, especially at high temperatures. To test this possibility in a potentially upward-colonizing species, we artificially incubated developing embryos of the viperine snake Natrix maura Linnaeus 1758, using a split-clutch design, in conditions of extreme high elevation or low elevation at two ecologically-relevant incubation temperatures (24 and 32 °C). Embryos at low and extreme high elevations incubated at cool temperatures did not differ in development time, hatchling phenotype or locomotor performance. However, at the warmer incubation temperature and at extreme high elevation, hatching success was reduced. Further, embryonic heart rates were lower, incubation duration longer and juveniles born smaller. Nonetheless, snakes in this treatment were faster swimmers than siblings in other treatment groups, suggesting a developmental trade-off between size and performance. Constraints on development may be offset by the maintenance of important performance metrics, thus suggesting that early life-history stages will not prevent the successful colonization of high-elevation habitat even under the dual limitations of reduced oxygen and increased temperature. [ABSTRACT FROM AUTHOR]

Much recent theoretical and empirical work has sought to describe the physiological mechanisms underlying thermal tolerance in animals. Leading hypotheses can be broadly divided into two categories that primarily differ in organizational scale: 1) high temperature directly reduces the function of subcellular machinery, such as enzymes and cell membranes, or 2) high temperature disrupts system-level interactions, such as mismatches in the supply and demand of oxygen, prior to having any direct negative effect on the subcellular machinery. Nonetheless, a general framework describing the contexts under which either subcellular component or organ system failure limits organisms at high temperatures remains elusive. With this commentary, we leverage decades of research on the physiology of ectothermic tetrapods (amphibians and non-avian reptiles) to address these hypotheses. Available data suggest both mechanisms are important. Thus, we expand previous work and propose the Hierarchical Mechanisms of Thermal Limitation (HMTL) hypothesis, which explains how subcellular and organ system failures interact to limit performance and set tolerance limits at high temperatures. We further integrate this framework with the thermal performance curve paradigm commonly used to predict the effects of thermal environments on performance and fitness. The HMTL framework appears to successfully explain diverse observations in reptiles and amphibians and makes numerous predictions that remain untested. We hope that this framework spurs further research in diverse taxa and facilitates mechanistic forecasts of biological responses to climate change. [ABSTRACT FROM AUTHOR]