The canonical model of sex-chromosome evolution predicts that, as recombination is suppressed along sex chromosomes, gametologs will progressively differentiate, eventually becoming heteromorphic. However, there are numerous examples of homomorphic sex chromosomes across the tree of life. This homomorphy has been suggested to result from frequent sex-chromosome turnovers, yet we know little about which forces drive them. Here, we describe an extremely fast rate of turnover among 28 species of Ranidae. Transitions are not random, but converge on several chromosomes, potentially due to genes they harbour. Transitions also preserve the ancestral pattern of male heterogamety, in line with the ‘hot-potato’ model of sex-chromosome transitions, suggesting a key role for mutation-load accumulation in non-recombining genomic regions. The importance of mutation-load selection in frogs might result from the extreme heterochiasmy they exhibit, making frog sex chromosomes differentiate immediately from emergence and across their entire length.
Non-recombining sex chromosomes are expected to undergo evolutionary decay,
ending up genetically degenerated, as has happened in birds and mammals. Why are
then sex chromosomes so often homomorphic in cold-blooded vertebrates? One
possible explanation is a high rate of turnover events, replacing master
sex-determining genes by new ones on other chromosomes. An alternative is that
X-Y similarity is maintained by occasional recombination events, occurring in
sex-reversed XY females. Based on mitochondrial and nuclear gene sequences, we
estimated the divergence times between European tree frogs (Hyla
arborea, H. intermedia, and H.
molleri) to the upper Miocene, about 5.4–7.1 million years
ago. Sibship analyses of microsatellite polymorphisms revealed that all three
species have the same pair of sex chromosomes, with complete absence of X-Y
recombination in males. Despite this, sequences of sex-linked loci show no
divergence between the X and Y chromosomes. In the phylogeny, the X and Y
alleles cluster according to species, not in groups of gametologs. We conclude
that sex-chromosome homomorphy in these tree frogs does not result from a recent
turnover but is maintained over evolutionary timescales by occasional X-Y
recombination. Seemingly young sex chromosomes may thus carry old-established
sex-determining genes, a result at odds with the view that sex chromosomes
necessarily decay until they are replaced. This raises intriguing perspectives
regarding the evolutionary dynamics of sexually antagonistic genes and the
mechanisms that control X-Y recombination.
In Europe, southern peninsulas served as refugia during cold periods in the Pleistocene, acting both as centres of origin of endemisms and as sources from which formerly glaciated areas were recolonized during interglacial periods. Previous studies have revealed that within the main refugial areas, intraspecific lineages often survived in allopatric refugia. We analysed two mitochondrial markers (nad4, control region, approximately 1.4 kb) in 103 individuals representing the entire distribution of Lissotriton boscai, a newt endemic to the western Iberian Peninsula. We inferred the evolutionary history of the species through phylogenetic, phylogeographic and historical demographic analyses. The results revealed unexpected, deep levels of geographically structured genetic variability. We identified two main evolutionary lineages, each containing three well-supported clades. The first historical split involved populations from central-southwestern coastal Portugal and the ancestor of all the remaining populations around 5.8 million years ago. Both lineages were subsequently fragmented into different population groups between 2.5 and 1.2 million years ago. According to nested clade analysis, at lower hierarchical levels the patterns suggest restricted gene flow with isolation by distance, whereas at higher levels the clades exhibit signatures of contiguous range expansion. Bayesian Skyline Plots show recent bottlenecks, followed by demographic expansions in all lineages. The significant genetic structure found is consistent with long-term survival of populations in allopatric refugia, supporting the 'refugia-within-refugia' scenario for southern European peninsulas. The comparison of our results with other co-distributed species highlights the generality of this hypothesis for the Iberian herpetofauna and suggests that Mediterranean refuges had more relevance for the composition and distribution of present biodiversity patterns than currently acknowledged. We briefly discuss the taxonomic and conservation implications of our results.
The last species list of the European herpetofauna was published by Speybroeck, Beukema and Crochet (2010). In the meantime, ongoing research led to numerous taxonomic changes, including the discovery of new species-level lineages as well as reclassifications at genus level, requiring significant changes to this list. As of 2019, a new Taxonomic Committee was established as an official entity within the European Herpetological Society, Societas Europaea Herpetologica (SEH). Twelve members from nine European countries reviewed, discussed and voted on recent taxonomic research on a case-by-case basis. Accepted changes led to critical compilation of a new species list, which is hereby presented and discussed. According to our list, 301 species (95 amphibians, 15 chelonians, including six species of sea turtles, and 191 squamates) occur within our expanded geographical definition of Europe. The list includes 14 non-native species (three amphibians, one chelonian, and ten squamates).
species tree analyses resolve the radiation of the widespread Bufo bufo species group (Anura, Bufonidae), Molecular Phylogenetics and Evolution (2011),
Chytridiomycosis is a fatal disease associated with amphibian population declines and extinctions worldwide. In a protected area in central Spain, the Peñalara Natural Park, the disease almost extirpated the population of Alytes obstetricans over only a few years, but did not apparently affect other amphibians. We present new observations documenting the occurrence of the disease in other species. In 2001–2003 we collected over 400 larvae or recently metamorphosed individuals of Salamandra salamandra and also several dead individuals of Bufo bufo. The analysis of the skin of post-metamorphic specimens revealed the presence of chytrid sporangia and discharge tubes in both species. According to measures of larval abundances in 1999 and 2003 the population of S. salamandra has suffered a marked decline but no significant trend was observed for B. bufo. We discuss the possible role of chytridiomycosis in the decline of S. salamandra and comment on the differential susceptibility exhibited by various species in the amphibian community at Peñalara.
Dispersal is a central process in ecology and evolution. It strongly influences the dynamics of spatially structured populations and affects evolutionary processes by shaping patterns of gene flow. For these reasons, dispersal has received considerable attention from ecologists, evolutionary biologists, and conservationists. Although it has been studied extensively in taxa such as birds and mammals, much less is known about 2 dispersal in vertebrates with complex life cycles such as pond-breeding amphibians. Over the past two decades, researchers have taken an ever-increasing interest in amphibian dispersal and initiated both basic and applied studies, using a broad range of experimental and observational approaches. This body of research reveals complex dispersal patterns, causations, and syndromes, with dramatic consequences for the demography and genetics of amphibian populations. In this review, our goals are to: redefine and clarify the concept of amphibian dispersal; review current knowledge about the effects of individual (i.e., condition-dependent dispersal) and environmental (i.e., context-dependent dispersal) factors during the three stages of dispersal (i.e., emigration, transience, and immigration); identify the demographic and genetic consequences of dispersal in spatially structured amphibian populations; and propose new research avenues to extend our understanding of amphibian dispersal.
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