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ABSTRACT Climate change can influence host–parasite dynamics by altering the abundance and distribution of hosts and their parasites as well as the physiology of both parasite and host. While the physiological effects of hosting parasites have been extensively studied in aquatic and laboratory model systems, these dynamics have been much less studied in wild terrestrial vertebrates, such as ectotherms that live in tropical forests. These organisms are particularly vulnerable to climate change because they have limited scope for behavioral buffering of stressful temperatures while already living at body temperatures close to their heat tolerance limits. Thus, it is imperative to understand how parasitism and tolerance to stressful thermal conditions, both of which are changing under climate warming, might interact to shape survival of non-model organisms. We measured heat tolerance and assessed endoparasites and ectoparasites in slender anole lizards (Anolis apletophallus; a lowland tropical forest species from central Panama). We then treated lizards with the antiparasitic drugs ivermectin and praziquantel and measured changes in immune function and heat tolerance compared with an unmanipulated control group. Immune function was not altered by treatment; however, heat tolerance increased in treated lizards. Additionally, higher endoparasite and ectoparasite abundance was associated with lower heat tolerance in a separate set of wild-caught lizards. Our results suggest that increasing environmental temperatures may have especially severe effects on host survival when parasites are present and highlight the need to consider interactions between thermal physiology and host–parasite dynamics when forecasting the responses of tropical animals to climate change. 

Abstract Human‐induced climate change, land use changes, and urbanization are predicted to dramatically impact landscape hydrology, which can have devastating impacts on aquatic organisms. For amphibians that rely on aquatic environments to breed and develop, it is essential to understand how the larval environment impacts development, condition, and performance later in life. Two important predicted impacts of climate change, urbanization, and land use changes are reduced hydroperiod and variable larval density. Here, we explored how larval density and hydroperiod affect development, morphology, physiology, and immune defenses at metamorphosis and 35 days post‐metamorphosis in the frogRana pipiens. We found that high‐density larval conditions had a large negative impact on development and morphology, which resulted in longer larval periods, reduced likelihood of metamorphosis, smaller size at metamorphosis, shorter femur to body length ratio, and reduced microbiome species evenness compared with animals that developed in low‐density conditions. However, animals from the high‐density treatment experienced compensatory growth post‐metamorphosis, demonstrating accelerated growth in body size and relative femur length compared with animals from the low‐density treatments, despite not “catching‐up” in size. We also observed an increase in relative gut length and relative liver size in animals that had developed in the high‐density treatment than those in the low‐density treatment, as well as higher bacterial killing ability, and greater jump distances relative to their leg length across different temperatures. Finally, metabolic rate was higher overall but especially at higher test temperatures for animals that developed under high‐density conditions, indicating that these animals may expend more energy in response to acute temperature changes. While the effects of climate change have direct negative effects on larval development and metamorphosis, animals can increase growth rate post‐metamorphosis; however, that compensatory growth might come at a cost and reduce their ability to cope with further environmental change such as increased temperatures.