A classic paradigm in evolutionary biology is that geographically isolated clades inhabiting similar selective regimes will diversify to create similar sets of phenotypes in different locations (e.g., similar stickleback species in different lakes, similar Anolis ecomorphs on different islands). Such parallel radiations are not generally expected to occur in sympatry because the available niche space would be filled by whichever clade is diversified first. Here, we document a very different pattern, the parallel evolution of similar body-size morphs in three sympatric clades of plethodontid salamanders (Desmognathus, Plethodon, Spelerpinae) in eastern North America. Using a comprehensive, time-calibrated phylogeny of North American plethodontids from nuclear and mitochondrial DNA sequences, we show that these three clades have undergone replicated patterns of evolution in body size and that this parallel diversification occurred in broad-scale sympatry. At the local scale, we find that coexisting species from these clades are more similar in body size than expected under a null model in which species are randomly assembled into communities.These patterns are particularly surprising in that competition is known to be important in driving phenotypic diversification and limiting local coexistence of similar-sized species within these clades. Although parallel diversification of sympatric clades may seem counterintuitive, we discuss several ecological and evolutionary factors that may allow the phenomenon to occur.

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Varanid lizards have been maintained in zoological parks for more than a century, yet few studies to date have attempted to pinpoint significant health issues affecting their management or areas of captive husbandry that are in need of improvement. In an effort to identify and better understand some of the husbandry-related challenges and health issues specifically affecting varanids in zoos, this study examined mortality in 16 species maintained at the Bronx Zoo between 1968 and 2009. Out of 108 records reviewed, complete necropsy reports were available for 85 individuals. Infection-related processes including bacterial (15.3%), protozoal (12.9%), nematode (9.4%), and fungal (3.5%) infections accounted for the greatest number of deaths (47.1%). Noninfectious diseases including female reproductive disorders (7.1%), neoplasia (7.1%), gout (10.8%), and hemipenal prolapse (1.3%) accounted for 29.4% of deaths. Multiple disease agents were responsible for 5.9% of deaths, and a cause for death could not be determined for 17.7% of individuals. Reproductive complications accounted for 11.5% of female deaths, but were identified in 23.1% of females. Although not necessarily the cause for death, gout was present in 18.8% of individuals. Differences in mortality between species, genders, and origin (captive-bred vs. wild-caught) were also evaluated. The results of this study corroborate earlier findings that identify bacterial infections, neoplasia, female reproductive disorders, gout, and endoparasitism as major sources of mortality in captive varanids. In light of these results, we discuss potential etiologies and offer recommendations for improving captive management practices in zoos.

In zoos, life expectancy-the average lifespan of individuals within a population, and longevity-the maximum lifespan within a population, can be useful parameters for evaluating captive husbandry and animal welfare. Using life history and demographic data derived from regional studbooks, this study examined life expectancy and longevity in a total of 782 wild-caught (WC) and captive-bred (CB) varanid lizards of seven species maintained in North American zoos since 1926. The average lifespans for WC and CB animals were 6.3 ± 0.3 and 9.3 ± 0.4 years, respectively, with CB males living significantly longer than females (P = 0.009). A total of 26.4% of WC and 22.5% of CB animals experienced mortality during their first 2 years in captivity, with mortality during this period greatest among Varanus rudicollis and V. prasinus. A positive correlation was observed between life expectancy and adult body mass in captive-bred individuals (r = 0.981; P = 0.002). Wild-caught females with a history of successful reproduction had a significantly greater average lifespan than non-reproducing females (P < 0.0001). Results from this study suggest that varanids have not been reaching their lifespan capacities in North American zoos. In light of these findings, several husbandry-related factors which may be affecting the welfare and lifespans of varanids in zoos are identified and discussed. This study also highlights the utility of demographic and life history data in captive animal management, and offers a general framework for future herpetological studies of a similar nature.