Summary1. Initial work on oxidative stress and antioxidant defences described basic chemical and biochemical properties and processes and applied this information to issues of animal health and husbandry. Seminal experimental investigations on the damaging effects of oxidative stress and the mitigating effects of antioxidant defences were conducted primarily in domesticated organisms. 2. In recent years, ecologists have taken to studying antioxidants and oxidative stress in free-ranging organisms and have integrated principles of oxidative stress into several core evolutionary concepts, such as life-history trade-offs (e.g. survival vs. reproduction), senescence and sexual selection. This initial flurry of studies has provided major advances in our understanding of how antioxidant defences evolve and function. 3. In this overview, it is our goal to provide ecologists with an accessible summary of (i) the biochemical basis and conceptual frameworks behind oxidative stress and antioxidants, (ii) the research questions and hypotheses that are generated by incorporating antioxidants and oxidative stress into models of life-history theory, ageing, mate selection, and honest signalling, and (iii) the trends in the evidence that have emerged from initial studies in these areas. 4. Though much progress has been made on the ecological and evolutionary relevance of antioxidant and oxidative stress physiology, no consensus has emerged regarding the primacy of how oxidative stress challenges or antioxidant limits or values shape organismal life-histories. However, there are many taxonomic biases in studies to date and several ideal environmental systems that are as-of-yet untapped.

The broad palette of feather colours displayed by birds serves diverse biological functions, including communication and camouflage. Fossil feathers provide evidence that some avian colours, like black and brown melanins, have existed for at least 160 million years (Myr), but no traces of bright carotenoid pigments in ancient feathers have been reported. Insight into the evolutionary history of plumage carotenoids may instead be gained from living species. We visually surveyed modern birds for carotenoid-consistent plumage colours (present in 2956 of 9993 species). We then used highperformance liquid chromatography and Raman spectroscopy to chemically assess the family-level distribution of plumage carotenoids, confirming their presence in 95 of 236 extant bird families (only 36 family-level occurrences had been confirmed previously). Using our data for all modern birds, we modelled the evolutionary history of carotenoid-consistent plumage colours on recent supertrees. Results support multiple independent origins of carotenoid plumage pigmentation in 13 orders, including six orders without previous reports of plumage carotenoids. Based on time calibrations from the supertree, the number of avian families displaying plumage carotenoids increased throughout the Cenozoic, and most plumage carotenoid originations occurred after the Miocene Epoch (23 Myr). The earliest origination of plumage carotenoids was reconstructed within Passeriformes, during the Palaeocene Epoch (66-56 Myr), and not at the base of crown-lineage birds.

Animal body temperature (Tbody) varies over daily and annual cycles, affecting multiple aspects of biological performance in both endothermic and ectothermic animals. Yet a comprehensive comparison of thermal performance among animals varying in Tbody (mean and variance) and heat production is lacking. Thus, we examined the thermal sensitivity of immune function (a crucial fitness determinant) in Vertebrata, a group encompassing species of varying thermal biology. Specifically, we investigated temperature-related variation in two innate immune performance metrics, hemagglutination and hemolysis, for 13 species across all seven major vertebrate clades. Agglutination and lysis were temperature dependent and were more strongly related to the thermal biology of species (e.g., mean Tbody) than to the phylogenetic relatedness of species, although these relationships were complex and frequently surprising (e.g., heterotherms did not exhibit broader thermal performance curves than homeotherms). Agglutination and lysis performance were positively correlated within species, except in taxa that produce squalamine, a steroidal antibiotic that does not lyse red blood cells. Interestingly, we found the antithesis of a generalist-specialist trade-off: species with broader temperature ranges of immune performance also had higher peak performance levels. In sum, we have uncovered thermal sensitivity of immune performance in both endotherms and ectotherms, highlighting the role that temperature and life history play in immune function across Vertebrata.

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Iridescent structures are some of the most visually stunning phenomena in biological organisms. Insects and birds have in common the display of such colours in their non-living investiture, the scales and bristles in insects and the feathers in birds. The biological mechanisms underlying the formation of these structures, at least in insects, appear quite conservative in that the same architect, the eukaryotic cell, can produce not only the iridescent structure but, with some tweaking of the genome, other structures as well, a fact that may be of particular interest to materials scientists and industrial parties seeking to biomimic these forms. Here, we review two examples, one on the cellular and the other on the subcellular level of this developmental flexibility in insects. We then go on to review what is known about iridescent feather development in birds. We suggest that, in view of the increasing evidence that genes and pathways are conserved among taxa, the work on insects may perhaps suggest perspectives or directions of potential use in the study of birds.