Miniaturization has been defined as the evolution of extremely small adult size in a lineage. It does not simply imply the decrease of the body size but also involves structural modifications to maintain functional efficiency at a strongly reduced size. Miniaturization has been proposed as a key factor in the origin of several major tetrapod clades. Current hypotheses propose that the living amphibians (lissamphibians) originated within a clade of Paleozoic dwarfed dissorophoid temnospondyls. Morphological traits shared by these small dissorophoids have been interpreted as resulting from constraints imposed by the extreme size reduction, but these statements were based only on qualitative observations. Herein, we assess quantitatively morphological changes in the skull previously associated with miniaturization in the lissamphibian stem lineage by comparing evolutionary and ontogenetic allometries in dissorophoids. Our results show that these features are not comparable to the morphological consequences of extreme size reduction as documented in extant miniature amphibians, but instead they resemble immature conditions of larger temnospondyls. We conclude that the truncation of the ancestral ontogeny, and not constraints related to miniaturization, might have been the factor that played a major role in the morphological evolution of small dissorophoids. Based on our results, we discuss the putative role of miniaturization in the origin of lissamphibians within Dissorophoidea.
Addressing the patterns of ontogenetic allometry is relevant to understand morphological diversification because allometry might constrain evolution to specific directions of change in shape but also facilitate phenotypic differentiation along lines of least evolutionary resistance. Temnospondyl amphibians are a suitable group to address these issues from a deep-time perspective because different growth stages are known for numerous Palaeozoic and Mesozoic species. Herein we examine the patterns of ontogenetic allometry in the skull roof of 15 temponspondyl species and their relationship with adult morphological evolution. Using geometric morphometrics, we assessed ontogenetic and evolutionary allometries of this cranial part and the distribution of adult shapes in the morphospace to investigate whether these patterns relate to each other and/or to lifestyle and phylogeny. We found conspicuous stereotyped ontogenetic changes of the skull roof which are mirrored at the evolutionary level and consistency of the adult shape with phylogeny rather than lifestyle. These results suggest that the evolution of adult cranial shape was significantly biased by development towards pathways patterned by ontogenetic change in shape. The retrieved conserved patterns agree with a widespread evolutionary craniofacial trend found in amniotes, suggesting that they might have originated early in tetrapod evolutionary history or even earlier.
Within the already peculiar Bauplan of anurans, pipid frogs have evolved an array of bizarre features that are commonly linked to their highly aquatic lifestyle. Among the latter, there are several distinctive sacro-caudo-pelvic features shared by extant pipids, which have been regarded as evolutionary novelties taking part of a specialized foreaft-sliding ilio-sacral joint. Pipids and their kin (pipimorphs) have a rich fossil record documenting 130 million years of uninterrupted evolution in aquatic environments, which, along with our current understanding of their phylogeny and recently available musculoskeletal data, allows us to inquire on the patterns and processes that have led to their distinctive sacro-caudo-pelvic system with a deep-time perspective. Here, we take a phylomorphospace approach based on discrete character matrices and a scaffold tree derived from recent studies, making comparisons of morphospace occupation between pipids and other anurans, and morphospace occupation, disparity, levels of homoplasy, and shared evolving characters between different groups and/or over time across pipimorphs. In doing so, we focus on trends of morphological diversification and discuss the potential role that ecological and developmental constraints might have had in driving the evolution of the sacro-caudo-pelvic complex of pipid frogs. Our main findings reveal a pattern of continuous and parallel innovation early in the history of pipids, followed by arrested evolution of novel morphologies toward the Recent. The latter, in turn, is mirrored by rampant homoplasy in the ilio-sacral sliding joint among extant pipid frogs. This study highlights the importance of fossils in revealing macroevolutionary patterns that will be otherwise veiled based on neontological data alone.
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