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Research focused on understanding the evolutionary factors that shape parity mode evolution among vertebrates have long focused on squamate reptiles (snakes and lizards), which contain all but one of the evolutionary transitions from oviparity to viviparity among extant amniotes. While most hypotheses have focused on the role of cool temperatures in favoring viviparity in thermoregulating snakes and lizards, there is a growing appreciation in the biogeographic literature for the importance of lower oxygen concentrations at high elevations for the evolution of parity mode. However, the physiological mechanisms underlying how hypoxia might reduce fitness, and how viviparity can alleviate this fitness decrement, has not been systematically evaluated. We qualitatively evaluated previous research on reproductive and developmental physiology, and found that (1) hypoxia can negatively affect fitness of squamate embryos, (2) oxygen availability in the circulatory system of adult lizards can be similar or greater than an egg, and (3) gravid females can possess adaptive phenotypic plasticity in response to hypoxia. These findings suggest that the impact of hypoxia on the development and physiology of oviparous and viviparous squamates would be a fruitful area of research for understanding the evolution of viviparity. To that end, we propose an integrative research program for studying hypoxia and the evolution of viviparity in squamates.

Predator-based selection has resulted in the repeated evolution of a variety of antipredator traits. Despite the effectiveness of these traits, some species experience shifts or even complete loss of antipredator traits during development. The evolutionary forces that favour such a transition are poorly understood. We sought to comprehend the role of predator-based selection and organismal factors underlying developmental loss of antipredator traits by focusing on decoy coloration in skink lizards. To this end, we studied the ontogenetic loss of decoy tail coloration in three Nearctic skink species. We performed natural history collection surveys and clay-model studies on predation to determine the organismal determinants of decoy coloration (body size and energy content of the tail) and predation based upon size and decoy coloration. We found that decoy coloration was lost during development at a similar size in all three species. Although predation rates on juvenile models were similar for both uniform brown and decoy models, predation rates on adult models with decoy coloration were much higher than those on non-decoy adult models. Overall, our results suggest that predator-based selection is an important factor driving the ontogenetic loss of decoy coloration at similar sizes across these species and might be generalizable to other antipredator traits.

Predator-prey interactions can be important drivers of morphological evolution, and antipredator traits in particular. Further, ecological context can be an important factor shaping the evolution of these traits. However, the role of ecological factors such as habitat structure in altering predator-based selection is not well known for antipredator traits such as decoy coloration. We used a combination of a natural history collection survey and a clay model experiment in open- and closed-canopy habitats to study how ecological context alters the fitness benefit of either red or blue decoy coloration in skinks. We found that the development and ecology of red decoy coloration of mole skinks differed substantially from blue tail coloration of other sympatric skink species. Mole skinks do not reach the body size of sympatric species of skinks and retain decoy coloration throughout development. Both patterns of scarring in museum specimens and attacks on plasticine models suggest that red coloration serves as a decoy, attracting attacks to the autotomous tail. While predation rates were similar across habitats, models with red tails were attacked far less frequently in open habitats than models with blue tails, while attack rates were similar in closed habitats. Our results suggest that red decoy coloration in mole skinks could be an adaptation to relatively open-canopy habitats. Our study has important implications for understanding how habitat structure and predator-based selection can alter the evolutionary dynamics of decoy coloration.

Viviparity, the bearing of live young, has evolved well over 100 times among squamate reptiles. This reproductive strategy is hypothesized to allow maternal control of the foetus' thermal environment and thereby to increase the fitness of the parents and offspring. Two hypotheses have been posited to explain this phenomenon: (i) the cold-climate hypothesis (CCH), which advocates low temperatures as the primary selective force; and (ii) the maternal manipulation hypothesis (MMH), which advocates temperature variability as the primary selective force. Here, we investigate whether climatic and geographic variables associated with the CCH vs. the MMH best explain the current geographical distributions of viviparity in lizards while incorporating recent advances in comparative methods, squamate phylogenetics and geospatial analysis. To do this, we compared nonphylogenetic and phylogenetic models predicting viviparity based on point-of-capture data from 20,994 museum specimens representing 215 lizard species in conjunction with spatially explicit bioclimatic and geographic (elevation and latitude) data layers. The database we analysed emphasized Nearctic lizards from three species-rich genera (Phrynosoma, Plestiodon and Sceloporus); however, we additionally analysed a less substantial, but worldwide sample of species to verify the universality of our Nearctic results. We found that maximum temperature of the warmest month (and, less commonly, elevation and maximum temperature of the driest quarter) was frequently the best predictor of viviparity and showed an association consistent with the CCH. Our results strongly favour the CCH over the MMH in explaining lizard reproductive mode evolution.

The Common Five-Lined Skink ( Plestiodon fasciatus ), Southeastern Five-Lined Skink ( P. inexpectatus ), and Broadheaded Skink ( P. laticeps ) are all found in forested ecosystems of the southeastern United States and occur in apparent sympatry. No aspect of their ecology has been quantitatively shown to be different. Differences in their natural history, such as northern extent of geographic range, observations of differences in habitat preference, and differing physiological responses to temperature, implicate the thermal environment as a potential niche dimension by which these organisms partition resources. Here we show that the northernmost extent of each species' range can be adequately discriminated by temperature extremes and that their preferred habitats differ in canopy cover, mean temperature, and daily maximum temperatures. These differences are supported by observations in the field. Based upon these findings and observations, we conclude that these species may be able to exist in such close proximity due to differences in their thermal niche, particularly the two like-sized species, P. fasciatus and P. inexpectatus. P. laticeps is a much larger lizard as an adult and functionally coexists with its congeners, potentially by partitioning resources along a different axis.

Three congeneric lizards from the southeastern United States (Plestiodon fasciatus, P. inexpectatus, and P. laticeps) exhibit a unique nested distribution. All three skink species inhabit the US Southeast, but two extend northward to central Ohio (P. fasciatus and P. laticeps) and P. fasciatus extends well into Canada. Distinct interspecific differences in microhabitat selection and behavior are associated with the cooler temperatures of the more Northern ranges. We hypothesized that interspecific differences in metabolic temperature sensitivity locally segregates them across their total range. Resting oxygen consumption was measured at 20°, 25° and 30°C. Plestiodon fasciatus, from the coolest habitats, exhibited greatly elevated oxygen consumption compared to the other species at high ecologically-relevant temperatures (0.10, 0.17 and 0.83 ml O2. g-1. h-1 at 20°, 25° and 30°C, respectively). Yet, P. inexpectatus, from the warmest habitats, exhibited sharply decreased oxygen consumption compared to the other species at lower ecologically-relevant temperatures (0.09, 0.27 and 0.42 ml O2. g-1. h-1 at 20°, 25° and 30°C, respectively). Plestiodon laticeps, from both open and closed microhabitats and intermediate latitudinal range, exhibited oxygen consumptions significantly lower than the other two species (0.057, 0.104 and 0.172 ml O2. g-1. h-1 at 20°, 25° and 30°C, respectively). Overall, Plestiodon showed metabolic temperature sensitivities (Q10s) in the range of 2–3 over the middle of each species’ normal temperature range. However, especially P. fasciatus and P. inexpectatus showed highly elevated Q10s (9 to 25) at the extreme ends of their temperature range. While morphologically similar, these skinks are metabolically distinct across the genus’ habitat, likely having contributed to their current distribution.