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Three genera of xenacanths, based on isolated teeth, occur in the lepospondyl (amphibian)−dominated fauna from the upper Black Prince Limestone (late Bashkirian). Orthacanthus donnelljohnsi sp. nov. teeth, with carinae lacking serrations on the compressed principal cusps, and only one intermediate cusp, represent both adult and juvenile teeth. Heterodonty occurs in both adult and juvenile dentitions. The absence of serrations is unique among Pennsylvanian species of Orthacanthus. Teeth with often highly asymmetrical bases with an aborally−flexed lingual marginal flange (= anterolingual shelf) and a single intermediate cusp are assigned to Triodus elpia sp. nov. A central foramen occurs in the base, unlike most other species; the moderately compressed principal cusps bear generally straight cristae. They represent the first reported occurrence of Triodus in the Paleozoic of North America. Five teeth, with cristae extending from the cusps onto their bases, belong to Bransonella. Two are questionably assigned to Bransonella nebraskensis, one to B. ?lingulata with its labio−lingually elongated apical button and smaller than normal intermediate cusp, and one each to Bransonella sp. “A” and “B”. Bransonella sp. “A” has a base wider (labio−lingual) than long, the reverse of the other Bransonella teeth. Bransonella sp. “B” is distinctly different, as it lacks an intermediate cusp (as in some B. lingulata teeth), and the basal tubercle is beneath one of the cusps (with no evidence of deformity).
Detailed studies on Carboniferous species of the xenacanth Orthacanthus have shown that the xenacanth dorsal fin spine can be used for skeletochronological analyses and provides valuable information about development, growth and environmental life conditions of those extinct sharks. We report here for the first time the histology and skeletochronology of Permian specimens, dorsal spines of Orthacanthus platypternus from the Craddock Bone Bed (lower Clear Fork Formation; Early Permian, Leonardian age) of northern Baylor County (north-central Texas, USA). Twelve dorsal spines of O. platypternus preserve a highly vascularized wall mainly composed of centrifugally growing dentine in a succession of dentine layers, probably deposited with an annual periodicity. As expected, spines of individuals with 1–2 dentine layers, presumably juveniles, present the smallest sizes. However, spines of individuals showing at least 3–4 dentine layers and interpreted to be subadults/young adults, are distributed in two spine-size clusters corresponding to females (probably the largest spines) and males, in agreement with the hypothesis of sexual size dimorphism proposed in a previous biometric analysis. Our comparative study of O. platypternus and the Stephanian species O. meridionalis further suggests that spine denticulation can be useful for distinguishing between species of Orthacanthus and sexually dimorphic forms (juvenile to adults) in each species. Total body length estimations of O. platypternus from the Craddock Bone Bed point to relatively large juveniles and small subadults/young adults (less than 2 m in total length), living as opportunistic predators in the pond-channel coastal plain environments represented by the bone bed deposits. The comparative analyses of the ontogenetic stages of the recorded specimens of O. platypternus and their distribution along different facies and localities indicate that this species was euryhaline, diadromous with a catadromous life-cycle which was strongly regulated by the semi-arid, seasonally dry tropical climate affecting western Pangaea during the Early Permian.
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