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We highlight some important conceptual issues that biologists should take into account when teaching evolutionary biology or communicating it to the public. We first present conclusions from conceptual development research on how particular human intuitions, namely design teleology and psychological essentialism, influence the understanding of evolution. We argue that these two intuitions form important conceptual obstacles to understanding evolution that should be explicitly addressed during instruction and public communication. Given that a major issue in evolution is understanding how very different forms may share common ancestry -antievolutionists have argued that this is inconceivable -we suggest that evolutionary developmental biology (evo-devo), which provides concepts and evidence that large morphological change is possible, could be used to address the intuitions that organisms have fixed essences (psychological essentialism) and that their structure indicates some kind of intentional design (design teleology).
We highlight some important conceptual issues that biologists should take into account when teaching evolutionary biology or communicating it to the public. We first present conclusions from conceptual development research on how particular human intuitions, namely design teleology and psychological essentialism, influence the understanding of evolution. We argue that these two intuitions form important conceptual obstacles to understanding evolution that should be explicitly addressed during instruction and public communication. Given that a major issue in evolution is understanding how very different forms may share common ancestry -antievolutionists have argued that this is inconceivable -we suggest that evolutionary developmental biology (evo-devo), which provides concepts and evidence that large morphological change is possible, could be used to address the intuitions that organisms have fixed essences (psychological essentialism) and that their structure indicates some kind of intentional design (design teleology).
Pelvic girdles, fins and claspers are evolutionary novelties first recorded in jawed vertebrates. Over the course of the evolution of chondrichthyans (cartilaginous fish) two trends in the morphology of the pelvic skeleton have been suggested to have occurred. These evolutionary shifts involved both an enlargement of the metapterygium (basipterygium) and a transition of fin radial articulation from the pelvic girdle to the metapterygium. To determine how these changes in morphology have occurred it is essential to understand the development of extant taxa as this can indicate potential developmental mechanisms that may have been responsible for these changes. The study of the morphology of the appendicular skeleton across development in chondrichthyans is almost entirely restricted to the historical literature with little contemporary research. Here, we have examined the morphology and development of the pelvic skeleton of a holocephalan chondrichthyan, the elephant shark (Callorhinchus milii), through a combination of dissections, histology, and nanoCT imaging and redescribed the pelvic skeleton of Cladoselache kepleri (NHMUK PV P 9269), a stem holocephalan. To put our findings in their evolutionary context we compare them with the fossil record of chondrichthyans and the literature on pelvic development in elasmobranchs from the late 19th century. Our findings demonstrate that the pelvic skeleton of C. milii initially forms as a single mesenchymal condensation, consisting of the pelvic girdle and a series of fin rays, which fuse to form the basipterygium. The girdle and fin skeleton subsequently segment into distinct components whilst chondrifying. This confirms descriptions of the early pelvic development in Scyliorhinid sharks from the historical literature and suggests that chimaeras and elasmobranchs share common developmental patterns in their pelvic anatomy. Alterations in the location and degree of radial fusion during early development may be the mechanism responsible for changes in pelvic fin morphology over the course of the evolution of both elasmobranchs and holocephalans, which appears to be an example of parallel evolution.
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