Abstract
Background†Saurichthyiformes were a successful group of latest Permian–Middle Jurassic predatory actinopterygian fishes and constituted important, widely-distributed components of Triassic marine and freshwater faunas. Their systematic affinities have long been debated, with †saurichthyiforms often being aligned with chondrosteans, a group today comprising sturgeons and paddlefishes. However, their character-rich endocranial anatomy has not been investigated in detail since the first half of the 20th century. Since then, major advances have occurred in terms of our understanding of early actinopterygian anatomy, as well as techniques for extracting morphological data from fossils.ResultsWe used μCT to study the internal cranial anatomy of two of the stratigraphically oldest representatives of †Saurichthys, from the Early Triassic of East Greenland and Nepal. Our work revealed numerous previously unknown characters (e.g., cryptic oticooccipital fissure; intramural diverticula of braincase; nasobasal canals; lateral cranial canal; fused dermohyal), and permitted the reevalution of features relating to the structure of cranial fossae, basicranial circulation and opercular anatomy of the genus. Critically, we reinterpret the former †saurichthyiform opercle as an expanded subopercle. For comparison, we also produced the first digital models of a braincase and endocast of a sturgeon (A. brevirostrum). New information from these taxa was included in a broad phylogenetic analysis of Actinopterygii. †Saurichthyiforms are resolved as close relatives of †Birgeria, forming a clade that constitutes the immediate sister group of crown actinopterygians. However, these and other divergences near the actinopterygian crown node are weakly supported.ConclusionsOur phylogeny disagrees with the historically prevalent hypothesis favoring the chondrostean affinities of †saurichthyiforms. Previously-proposed synapomorphies uniting the two clades, such as the closure of the oticooccipital fissure, the posterior extension of the parasphenoid, and the absence of an opercular process, are all widespread amongst actinopterygians. Others, like those relating to basicranial circulation, are found to be based on erroneous interpretations. Our work renders the †saurichthyiform character complex adequately understood, and permits detailed comparisons with other stem and crown actinopterygians. Our phylogenetic scheme highlights outstanding questions concerning the affinity of many early actinopterygians, such as the Paleozoic–early Mesozoic deep-bodied forms, which are largely caused by lack of endoskeletal data.
Highlights
Actinopterygii, with more than 32,000 living species [1], encompass over half of extant vertebrate species and possess an evolutionary history of at least 415 myr [2, 3]
Our phylogeny disagrees with the historically prevalent hypothesis favoring the chondrostean affinities of †saurichthyiforms
Fossil age and locality information The Early Triassic (Induan: Griesbachian–early Dienerian; see [55]) Wordie Creek Formation of East Greenland contains six well-demarcated horizons (‘Fish Zones I–V’, ‘Stegocephalian Zone’ [56]) that yielded a plethora of vertebrate fossils, including a sizable fossil fish sample, dominated by actinopterygians [56,57,58,59,60,61]
Summary
Actinopterygii (ray-finned fishes), with more than 32,000 living species [1], encompass over half of extant vertebrate species and possess an evolutionary history of at least 415 myr [2, 3] This extant diversity is unevenly distributed among three major clades: Cladistia (bichirs and the reedfish), Chondrostei (sturgeons and paddlefishes), and Neopterygii, the latter containing the depauperate Holostei (gars and the bowfin) and the very speciose Teleostei [4, 5]. Abundant fossil actinopterygians of Paleozoic and early Mesozoic age are known [13,14,15], but their systematic placement relative to neopterygians, chondrosteans, and cladistians is highly unstable and variable between phylogenetic analyses [12, 16,17,18,19,20]. Some of this ambiguity doubtlessly reflects genuine character conflict, the limited documentation of anatomy in many fossils of this age presents the chief obstacle
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