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Batesian mimicry, in which harmless species (mimics) deter predators by deceitfully imitating the warning signals of noxious species (models), generates striking cases of phenotypic convergence that are classic examples of evolution by natural selection. However, mimicry of venomous coral snakes has remained controversial because of unresolved conflict between the predictions of mimicry theory and empirical patterns in the distribution and abundance of snakes. Here we integrate distributional, phenotypic and phylogenetic data across all New World snake species to demonstrate that shifts to mimetic coloration in nonvenomous snakes are highly correlated with coral snakes in both space and time, providing overwhelming support for Batesian mimicry. We also find that bidirectional transitions between mimetic and cryptic coloration are unexpectedly frequent over both long- and short-time scales, challenging traditional views of mimicry as a stable evolutionary 'end point' and suggesting that insect and snake mimicry may have different evolutionary dynamics.

Aim: The aim was to determine how reptile populations respond to anthropogenic habitat modification and determine whether species traits and environmental factors influence such responses. Location: Global. Time period: 1981–2018. Major taxa studied: Squamata. Methods: We compiled a database of 56 studies reporting how habitat modification affects reptile abundance and calculated standardized mean differences in abundance (Hedges' g). We used Bayesian meta‐analytical models to test whether responses to habitat modification depended on body size, clutch size, reproductive mode, habitat specialization, range size, disturbance type, vegetation type, temperature and precipitation. Results: Based on 815 effect sizes from 376 species, we found an overall negative effect of habitat modification on reptile abundance (mean Hedges' g = −0.43, 95% credible intervals = −0.61 to −0.26). Reptile abundance was, on average, one‐third lower in modified compared with unmodified habitats. Small range sizes and small clutch sizes were associated with more negative responses to habitat modification, although the responses were weak and the credible intervals overlapped zero. We detected no effects of body size, habitat specialization, reproductive mode (egg‐laying or live‐bearing), temperature or precipitation. Some families exhibited more negative responses than others, although overall there was no phylogenetic signal in the data. Mining had the most negative impacts on reptile abundance, followed by agriculture, grazing, plantations and patch size reduction, whereas the mean effect of logging was neutral. Main conclusions: Habitat modification is a key cause of reptile population declines, although there is variability in responses both within and between species, families and vegetation types. The effect of disturbance type appeared to be related to the intensity of habitat modification. Ongoing development of environmentally sustainable practices that ameliorate anthropogenic impacts is urgently needed to prevent declines in reptile populations. [ABSTRACT FROM AUTHOR]

Viviparity (live‐bearing) has independently evolved from oviparity (egg‐laying) in more than 100 lineages of squamates (lizards and snakes).We might expect consequent shifts in selective forces to affect per‐brood reproductive investment (RI = total mass of offspring relative to maternal mass) and in the way in which that output is partitioned (number vs. size of offspring per brood). Based on the assumption that newly born offspring are heavier than eggs, we predicted that live‐bearing must entail either increased RI or a reduction in offspring size and/or fecundity.However, our phylogenetically controlled analysis of data on 1,259 squamate species revealed no significant differences in mean offspring size, clutch size or RI between oviparous and viviparous squamates.We attribute this paradoxical result to (1) strong selection on offspring sizes, unaffected by parity mode, (2) the lack of a larval stage in amniotes, favouring large eggs even in the ancestral oviparous mode and (3) the ability of viviparous females to decrease the mass of uterine embryos by reducing extra‐embryonic water stores.Our analysis shows that squamate eggs (when laid) weigh about the same as the hatchlings that emerge from them (despite a many‐fold increase in embryo mass during incubation). Most of the egg mass is due to components (such as water stores and the eggshell) not required for oviductal incubation. That repackaging enables live‐born offspring to be accommodated within the mother's body without increasing total litter mass.The consequent stasis in reproductive burden during the evolutionary transition from oviparity to viviparity may have facilitated frequent shifts in parity modes. [ABSTRACT FROM AUTHOR]

Aim To map and assess the richness patterns of reptiles (and included groups: amphisbaenians, crocodiles, lizards, snakes and turtles) in Africa, quantify the overlap in species richness of reptiles (and included groups) with the other terrestrial vertebrate classes, investigate the environmental correlates underlying these patterns, and evaluate the role of range size on richness patterns. Location Africa. Methods We assembled a data set of distributions of all African reptile species. We tested the spatial congruence of reptile richness with that of amphibians, birds and mammals. We further tested the relative importance of temperature, precipitation, elevation range and net primary productivity for species richness over two spatial scales (ecoregions and 1° grids). We arranged reptile and vertebrate groups into range-size quartiles in order to evaluate the role of range size in producing richness patterns. Results Reptile, amphibian, bird and mammal richness are largely congruent ( r = 0.79-0.86) and respond similarly to environmental variables (mainly productivity and precipitation). Ecoregion size accounts for more variation in the richness of reptiles than in that of other groups. Lizard distributions are distinct with several areas of high species richness where other vertebrate groups (including snakes) are species-poor, especially in arid ecoregions. Habitat heterogeneity is the best predictor of narrow-ranging species, but remains relatively important in explaining lizard richness even for species with large range sizes. Main conclusions Reptile richness varies with similar environmental variables as the other vertebrates in Africa, reflecting the disproportionate influence of snakes on reptile richness, a result of their large ranges. Richness gradients of narrow-ranged vertebrates differ from those of widespread taxa, which may demonstrate different centres of endemism for reptile subclades in Africa. Lizard richness varies mostly with habitat heterogeneity independent of range size, which suggests that the difference in response of lizards is due to their ecological characteristics. These results, over two spatial scales and multiple range-size quartiles, allow us to reliably interpret the influence of environmental variables on patterns of reptile richness and congruency. [ABSTRACT FROM AUTHOR]

Vertebrate sex-determining mechanisms ( SDMs) are triggered by the genotype ( GSD), by temperature ( TSD), or occasionally, by both. The causes and consequences of SDM diversity remain enigmatic. Theory predicts SDM effects on species diversification, and life-span effects on SDM evolutionary turnover. Yet, evidence is conflicting in clades with labile SDMs, such as reptiles. Here, we investigate whether SDM is associated with diversification in turtles and lizards, and whether alterative factors, such as lifespan's effect on transition rates, could explain the relative prevalence of SDMs in turtles and lizards (including and excluding snakes). We assembled a comprehensive dataset of SDM states for squamates and turtles and leveraged large phylogenies for these two groups. We found no evidence that SDMs affect turtle, squamate, or lizard diversification. However, SDM transition rates differ between groups. In lizards TSD-to- GSD surpass GSD-to- TSD transitions, explaining the predominance of GSD lizards in nature. SDM transitions are fewer in turtles and the rates are similar to each other ( TSD-to- GSD equals GSD-to- TSD), which, coupled with TSD ancestry, could explain TSD's predominance in turtles. These contrasting patterns can be explained by differences in life history. Namely, our data support the notion that in general, shorter lizard lifespan renders TSD detrimental favoring GSD evolution in squamates, whereas turtle longevity permits TSD retention. Thus, based on the macro-evolutionary evidence we uncovered, we hypothesize that turtles and lizards followed different evolutionary trajectories with respect to SDM, likely mediated by differences in lifespan. Combined, our findings revealed a complex evolutionary interplay between SDMs and life histories that warrants further research that should make use of expanded datasets on unexamined taxa to enable more conclusive analyses. [ABSTRACT FROM AUTHOR]

Aim Size is one of the most important and obvious traits of an organism. Both small and large sizes have adaptive advantages and disadvantages. Body size-frequency distributions of most large clades are unimodal and right skewed. Species larger than the mean or range midpoint of body sizes are relatively scarce. Theoretical models suggest evolutionary rates are higher in small organisms with short generation times. Therefore diversification rates are usually thought to be maximal at relatively small body sizes. Empirical studies of the rates of molecular evolution and clade diversification, however, have usually indicated that both are unrelated to body size. Furthermore, it has been claimed that because snakes are longer than lizards, the size-frequency distribution of all squamate species is bimodal overall. We examined the shape of the size-frequency distribution of nearly all Squamata and Rhynchocephalia species, and investigated how size affected diversification rates. Location Global. Methods We collected data on maximum body length for 9805 lepidosaur (squamates and the tuatara) species (99.7% of all species) and converted them to mass using clade-specific allometric equations. Using methods that test for relationships between continuous traits and speciation and extinction rates on a large, dated phylogeny (4155 species), we investigated the relationship between diversification rates and body size. Results Living squamates span six orders of magnitude in body size, eight when giant extinct snakes and mosasaurs are included. The body size-frequency distributions of snakes and lizards separately, and of all lepidosaur species combined, are unimodal and right skewed. Nonetheless, we find neither linear nor hump-shaped relationships between size and diversification rates, except in snakes, where speciation and diversification are hump shaped. Main conclusions Despite a clear modality and skew in the body sizes of lepidosaurs, we find little evidence for faster diversification of modal-sized taxa, perhaps implying that larger-sized clades are relatively young. [ABSTRACT FROM AUTHOR]

Aim Islands organisms usually have fewer predator and competitor species than mainland ones. This is thought to result in high population densities on islands. We hypothesize that insular lizards have denser populations than mainland species and that density, in general, is negatively correlated with competitor and predator richness. Location Global. Methods We compared densities of 346 lizard species on islands and the mainland while examining the relationship between density and, predator and competitor richness, primary productivity, seasonality and island area. We controlled for phylogenetic non-independence, body mass and study area, which are known to strongly affect population density. Results Insular populations (especially on snake-free islands) are denser than mainland ones. Mainland populations of lizard species that also inhabit islands were denser than those of species that do not inhabit islands. Population density was the highest on islands with low net primary productivity and was not significantly affected by competitor or predator richness. Moreover, insular populations show high density regardless of island area. Main conclusions We conclude that the ability of mainland species to reach high population densities may increase their chances in reaching and successfully colonizing islands. We postulate that population density may be affected by predator and competitor density rather than by their richness. Density increase on islands may result not from the environmental simplicity of island faunas but through propagule sorting or pressure. [ABSTRACT FROM AUTHOR]

We describe the finding, in a museum jar, of the sixth known specimen of the Eritrean snake Platyceps largeni (Scätti, 2001) (synonym, Coluber largeni). The specimen is from Museri Island, Dahlak Archipelago in the Red Sea. This record is the first one for this island and it represents a ca. 50 km range extension of this species, hitherto known from five specimens in a tight cluster of three other islands. This find verifies Schätti's (2001) prediction that the species might be found in the nearby archipelago islands. [ABSTRACT FROM AUTHOR]