RESUMO
Among tetrapods, viviparity is estimated to have evolved independently within Squamata (lizards and snakes) more than 100 times, most frequently in species occupying cold climate environments. Because of this relationship with cold climates, it is sometimes assumed that many origins of squamate viviparity occurred over the past 2.5-4 Myr during the Pliocene-Pleistocene glaciations; however, this hypothesis is untested. Divergence-dating analysis on a 733-species tree of Iguanian lizards recovers 20 independent lineages that have evolved viviparity, of which 13 multispecies groups derived live birth prior to glacial advances (8-66 Myr ago). These results place the transitions from egg-laying to live birth among squamates in a well-supported historical context to facilitate examination of the underlying phenotypic and genetic changes associated with this complex shift in reproduction.
Assuntos
Adaptação Biológica/fisiologia , Evolução Biológica , Iguanas/fisiologia , Filogenia , Viviparidade não Mamífera/fisiologia , Animais , Sequência de Bases , Biologia Computacional , Primers do DNA/genética , Feminino , Funções Verossimilhança , Modelos Genéticos , Dados de Sequência Molecular , Alinhamento de Sequência , Análise de Sequência de DNARESUMO
George Gaylord Simpson famously postulated that much of life's diversity originated as adaptive radiations-more or less simultaneous divergences of numerous lines from a single ancestral adaptive type. However, identifying adaptive radiations has proven difficult due to a lack of broad-scale comparative datasets. Here, we use phylogenetic comparative data on body size and shape in a diversity of animal clades to test a key model of adaptive radiation, in which initially rapid morphological evolution is followed by relative stasis. We compared the fit of this model to both single selective peak and random walk models. We found little support for the early-burst model of adaptive radiation, whereas both other models, particularly that of selective peaks, were commonly supported. In addition, we found that the net rate of morphological evolution varied inversely with clade age. The youngest clades appear to evolve most rapidly because long-term change typically does not attain the amount of divergence predicted from rates measured over short time scales. Across our entire analysis, the dominant pattern was one of constraints shaping evolution continually through time rather than rapid evolution followed by stasis. We suggest that the classical model of adaptive radiation, where morphological evolution is initially rapid and slows through time, may be rare in comparative data.