Background Dakosaurus and Plesiosuchus are characteristic genera of aquatic, large-bodied, macrophagous metriorhynchid crocodylomorphs. Recent studies show that these genera were apex predators in marine ecosystems during the latter part of the Late Jurassic, with robust skulls and strong bite forces optimized for feeding on large prey.Methodology/Principal FindingsHere we present comprehensive osteological descriptions and systematic revisions of the type species of both genera, and in doing so we resurrect the genus Plesiosuchus for the species Dakosaurus manselii. Both species are diagnosed with numerous autapomorphies. Dakosaurus maximus has premaxillary ‘lateral plates’; strongly ornamented maxillae; macroziphodont dentition; tightly fitting tooth-to-tooth occlusion; and extensive macrowear on the mesial and distal margins. Plesiosuchus manselii is distinct in having: non-amblygnathous rostrum; long mandibular symphysis; microziphodont teeth; tooth-crown apices that lack spalled surfaces or breaks; and no evidence for occlusal wear facets. Our phylogenetic analysis finds Dakosaurus maximus to be the sister taxon of the South American Dakosaurus andiniensis, and Plesiosuchus manselii in a polytomy at the base of Geosaurini (the subclade of macrophagous metriorhynchids that includes Dakosaurus, Geosaurus and Torvoneustes).Conclusions/SignificanceThe sympatry of Dakosaurus and Plesiosuchus is curiously similar to North Atlantic killer whales, which have one larger ‘type’ that lacks tooth-crown breakage being sympatric with a smaller ‘type’ that has extensive crown breakage. Assuming this morphofunctional complex is indicative of diet, then Plesiosuchus would be a specialist feeding on other marine reptiles while Dakosaurus would be a generalist and possible suction-feeder. This hypothesis is supported by Plesiosuchus manselii having a very large optimum gape (gape at which multiple teeth come into contact with a prey-item), while Dakosaurus maximus possesses craniomandibular characteristics observed in extant suction-feeding odontocetes: shortened tooth-row, amblygnathous rostrum and a very short mandibular symphysis. We hypothesise that trophic specialisation enabled these two large-bodied species to coexist in the same ecosystem.
Machimosaurus was a large-bodied genus of teleosaurid crocodylomorph, considered to have been durophagous/chelonivorous, and which frequented coastal marine/estuarine ecosystems during the Late Jurassic. Here, we revise the genus based on previously described specimens and revise the species within this genus. We conclude that there were three European Machimosaurus species and another taxon in Ethiopia. This conclusion is based on numerous lines of evidence: craniomandibular, dental and postcranial morphologies; differences in estimated total body length; geological age; geographical distribution; and hypothetical lifestyle. We re-diagnose the type species Machimosaurus hugii and limit referred specimens to only those from Upper Kimmeridgian–Lower Tithonian of Switzerland, Portugal and Spain. We also re-diagnose Machimosaurus mosae, demonstrate that it is an available name and restrict the species to the uppermost Kimmeridgian–lowermost Tithonian of northeastern France. We re-diagnose and validate the species Machimosaurus nowackianus from Harrar, Ethiopia. Finally, we establish a new species, Machimosaurus buffetauti, for the Lower Kimmeridgian specimens of France and Germany (and possibly England and Poland). We hypothesize that Machimosaurus may have been analogous to the Pliocene–Holocene genus Crocodylus in having one large-bodied taxon suited to traversing marine barriers and additional, geographically limited taxa across its range.
A new hadrosaurid dinosaur, Arenysaurus ardevoli gen. et sp. nov., from the Late Maastrichtian of Aren (Huesca, South-central Pyrenees) is described on the basis of a partial, articulated skull, mandibular remains and postcranial elements, including vertebrae, girdle and limb bones. Arenysaurus is characterized by having a very prominent frontal dome; nearly vertical prequadratic (squamosal) and jugal (postorbital) processes, and deltopectoral crest of the humerus oriented anteriorly. Moreover, it possesses a unique combination of characters: short frontal (length/width approximately 0.5); midline ridge of parietal at level of the postorbitalsquamosal bar; parietal excluded from the occiput; squamosal low above the cotyloid cavity. A phylogenetical analysis indicates that Arenysaurus is a rather basal member of Lambeosaurinae and the sister-taxon to Amurosaurus and the Corythosaurini-
Six new dinosaurs sites have been found close to the Cretaceous/Tertiary boundary in Arén (south-central Pyrenees, Huesca, Spain) in coastal and non-marine deposits of the Arén and Tremp Formations. The sites contain articulated remains (skull elements, vertebrae, hind-limb bones) and isolated teeth and bones of hadrosaurids, three types of theropod teeth, one sauropod, at least seven types of eggshells (six ornithoid types and one Megaloolithidae probably from a sauropod), remains of other vertebrates, and four charophyte species. The fossil-bearing rocks have been correlated with marine sediments containing planktonic foraminifera from the uppermost Maastrichtian Abathomphalus mayaroensis Biozone. These rich and diversified dinosaur assemblages enable more accurate dating of the faunal changes that took place during the Maastrichtian in Europe and support the hypothesis of a sudden dinosaur extinction at the Cretaceous/Tertiary boundary. Academic Press
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