Heterochrony and Oophagy Underlie the Evolution of Giant Filter-Feeding Lamniform Sharks

IF 2.6 3区 生物学 Q2 DEVELOPMENTAL BIOLOGY
Joel H. Gayford, Duncan J. Irschick, Andrew Chin, Jodie L. Rummer
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引用次数: 0

Abstract

Evolutionary transitions toward gigantic body sizes have profound consequences for the structure and dynamics of ecological networks. Among elasmobranchs (sharks and rays), gigantism has evolved on several occasions, most notably in the iconic Megalodon (Otodus megalodon†) and the extant whale shark (Rhincodon typus), basking shark (Cetorhinus maximus), and megamouth shark (Megachasma pelagios), all of which reach total lengths exceeding 6 m and, in some cases, reach 21 m or more. Comparative phylogenetic studies suggest that filter feeding and heterothermy provide two alternative evolutionary pathways leading to gigantism in sharks. These selection-based explanations for gigantism are important; however, our understanding of evolutionary transitions in body size is fundamentally constrained without a proximate, mechanistic understanding of how the suite of adaptations necessary to facilitate gigantism evolved. Here we propose the heterochrony hypothesis for the evolution of the giant filter-feeding shark ecomorphotype. We suggest that craniofacial adaptations for oophagy in embryonic stages of lamniform sharks are retained through ontogeny in C. maximus and M. pelagios by paedomorphosis, resulting in an enlarged head and mouth relative to the rest of the body, even in adulthood. This change in developmental timing enables these taxa to optimize prey acquisition, which is thought to be the limiting factor for the evolution of gigantism in filter-feeding marine vertebrates. We discuss the concordance of this hypothesis with current developmental, morphological, and evolutionary data, and we suggest future means by which the hypothesis could be tested.

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来源期刊
Evolution & Development
Evolution & Development 生物-发育生物学
CiteScore
6.30
自引率
3.40%
发文量
26
审稿时长
>12 weeks
期刊介绍: Evolution & Development serves as a voice for the rapidly growing research community at the interface of evolutionary and developmental biology. The exciting re-integration of these two fields, after almost a century''s separation, holds much promise as the focus of a broader synthesis of biological thought. Evolution & Development publishes works that address the evolution/development interface from a diversity of angles. The journal welcomes papers from paleontologists, population biologists, developmental biologists, and molecular biologists, but also encourages submissions from professionals in other fields where relevant research is being carried out, from mathematics to the history and philosophy of science.
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