In dense mating aggregations, such as insect and anuran choruses, signals produced at the same time can overlap and interfere with one another, reducing the ability of receivers to discriminate between individual signals. Thus, evolution by sexual selection is expected to result in mating signal timing strategies that avoid overlap. Patterns of signal alternation between competing males are commonly observed in leks and choruses across taxa. In some species, however, signalers instead deliberately overlap, or ‘synchronize’, their mating signals with neighboring conspecifics. Given the assumed high cost of reduced mate attraction when signals overlap, mating signal synchronization has remained an evolutionary puzzle. Synchronization may be beneficial, however, if overlapping signals reduce the attraction of nontarget receivers (predator avoidance hypothesis). Synchronized signals could also constructively interfere, increasing female attraction to the mating aggregation (the beacon effect hypothesis). I investigate these functions of synchronized signaling in two species of tree frogs that synchronize their mating calls: the pug-nosed tree frog (<i>Smilisca sila</i>) and the Ryukyu Kajika frog (<i>Buergeria japonica</i>). To examine the trade-offs imposed by call synchronization in each species, I conduct a series of field and laboratory playback experiments on target (female frogs) and nontarget (eavesdropping predators) receivers of frog calls. Results from these experiments support both hypotheses, suggesting that synchronized frog calls can reduce the attraction of predators and attract mates to the chorus. In addition, I found reduced preferences for fine-scale call timings in female <i>S. sila</i> and <i>B. japonica</i>, deviating from the expected preferences observed in many other anuran and non-anuran species. Thus, while males may enjoy multiple benefits from synchronized mating signals, relaxed sexual selection for non-synchronous signals may be key to the evolution and maintenance of mating signal synchrony.

<p> Per- and polyfluoroalkyl substances (PFAS) are a class of persistent environmental contaminants that have become ubiquitous, resulting in widespread exposure among humans and wildlife. Amphibians are regularly exposed in the field, making them susceptible to sublethal effects of PFAS exposure. In amphibians exposed to PFAS, deleterious effects have been observed, including reduction in body condition measured using the scaled mass index (SMI) and degraded hepatic condition, among others. PFAS may dysregulate lipid metabolism by altering signaling cascades regulated by peroxisome proliferator activated receptors (PPAR), but whether changes in energy stores can explain changes in amphibian SMI and/or hepatic condition remain underexplored. Since lipids are a critical energy reserve for anurans, understanding whether lipid metabolism is being perturbed is critical. The central objective of this thesis was to investigate the effect of PFAS on lipid homeostasis in <em>Xenopus laevis </em>tadpoles within the context of a PPAR mechanism of action (MOA), considering apical, molecular, and lipidomic endpoints. I conducted three studies: (a) a study to characterize SMI and the relative expression of the hepatic xPPARα/β/γ during metamorphosis, (b) a pharmaceutical exposure to assess the <em>in vivo</em> effects of xPPARα/β/γ agonism on hepatic gene expression for select downstream targets (<em>apoa5, fabp1, acox1,​ pck1</em>), and (c) a chronic PFAS exposure to investigate the effects of environmentally relevant concentrations (PFOS, PFHxS, PFOA, PFHxA at 0.5 ppb; binary mixture of PFOS:PFHxS at 1 ppb) on lipid homeostasis through apical endpoints (mass, snout vent length, SMI, hepatic condition), relative hepatic gene expression, and Multiple Reaction Monitoring (MRM) profiling of the hepatic lipidome for changes in relative class abundance. In study (a), I identified SMI and hepatic expression of <em>xPPARα/β/γ</em> is dynamic during late metamorphosis, indicating the potential for heightened susceptibility. However, in study (b), pharmaceutical agonists had no effect on <em>X. laevis</em> at high doses. For study (c), I did not observe effects on a majority of apical endpoints, including SMI, but detected a significant sex-specific reduction in hepatic condition for male<em> X. laevis</em> tadpoles exposed to single-chemical perfluorosulfonic acid (PFSA) treatments. For gene expression, I observed a transient downregulation for apolipoprotein-V (<em>apoa5</em>) at Nieuwkoop and Faber (NF) stage 62 for <em>X. laevis</em> tadpoles exposed to single-chemical perfluorocarboxylic acid (PFCA) treatments. Lipid profiling detected transient dysregulation of predominantly membrane lipids in-response to short-chain PFAS treatments at NF 58. Overall, our findings indicate PFAS may exert toxicity during anuran metamorphosis through multiple mechanisms of action (MOA) with sex-specific and developmental-stage specific outcomes.</p>