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The relatively rich assemblages of shark teeth from pelagic limestone (Mississippian, late Viséan, late Asbian-middle Brigantian) of three northern European regions: the Rhenish Mountains (Westenfeld Quarry, Germany), the Holy Cross Mountains (Todowa Grząba at the edge of Ostrówka Quarry, Poland), and Derbyshire (Cawdor Quarry, Matlock, England, UK) display certain similarities, with the absolute predominance of the teeth of Falcatidae (small Symmoriiformes) and the constant presence of Thrinacodus spp. The largest and most diverse assemblage from Todowa Grząba contains at least three species of a falcatid Denaea, a xenacanthimorph Bransonella nebraskensis, a newly described phoebodontid Thrinacodus dziki sp. nov., a few ctenacanthiform and euselachian teeth, and two abraded euchondrocephalan dental elements. Anachronistidae, common in the most of late Viséan pelagic faunas, are absent from Todowa Grząba and Westenfeld. The material under study differs from the shallow-water chondrichthyan fauna, hitherto described from the Mississippian carbonate platform facies, by its taxonomic content (particularly almost total absence of Euchondro-cephali), generally lower diversity, and higher frequency of small teeth.
Listracanthus pectenatus sp. nov. represents the youngest record of the enigmatic chondrichthyan Listracanthus. This new species is the only Mesozoic record of this genus and highlights survival of a rare and enigmatic group of cartilaginous fishes across the Paleozoic–Mesozoic boundary. In the Vega−Phroso Siltstone Member of the Sulphur Mountain Formation (western Canada), two kinds of numerous dermal denticles identified as Listracanthus occur predominantly in strata probably of early Smithian age. The new species differs from all other known species of the genus in the structure of the anterior and posterior borders of the large denticles. The small denticles appear to be less diagnostic than the large ones and are readily distinguished from small denticles generally assigned to the genus Petrodus. Histology reveals that the largest denticles were originally hollow, probably secondarily ossified as acellular bone. The conclusion drawn by previous authors that Listracanthus may be a petalodontid shark, based on ambiguous non−skeletal associations with Deltoptychius, Petrodus, or Calopodusis not supported by this study. The large number of denticles, the size of both types of denticles and their arrangement suggest that Listracanthus pectenatus sp. nov. was a large chondrichthyan of aberrant body shape and yet uncertain systematic position.
Sampling of latest Burdigalian (Miocene) silty clays from the Malé Karpaty Mountains in the Slovakia revealed a deep−water, low diversity shark fauna. The fauna is dominated by teeth of very small squaliform sharks, including two new species, Eosqualiolus skrovinai sp. nov. and Paraetmopterus horvathi sp. nov. The generic composition of the squaliform fauna is more similar to that known from the Eocene than that of today, suggesting a post–early Miocene faunal turnover within this clade, at least locally. Nectobenthic, non squaliform sharks are rare, but include the new sawshark species Pristiophorus striatus sp. nov., while minute teeth of an enigmatic taxon described here as Nanocetorhinus tuberculatus gen. et sp. nov. probably indicate the presence of a previously unrecorded planktivore. The unusual composition of the fauna, with the complete absence of taxa known to be of medium to large size, suggests an unusual, and probably very stressed, palaeoenvironment.
The shallow water assemblage of chondrichthyan microremains, teeth, tooth plates and scales, from the middle Tournaisian (Mississippian) of the vicinity of Muhua village, Guizhou province, southern China, is thus far the richest and most diverse association of this age collected from a single locality and horizon, and represents a chondrichthyan community very restricted in time and space. It was recovered from a small bioclastic limestone lens, MH−1, occurring among basinal marls near the base of the Muhua Formation, and dated as to the Siphonodella crenulata conodont Zone. The majority of the fauna presented here consists of teeth with euselachian−type bases and crushing crowns belonging to bottom−dwelling durophagous chondrichthyans, most probably feeding on shelly invertebrates such as the abundant brachiopods. We assigned most of these teeth to Euselachii (six species, among them Cassisodus margaritae gen. et sp. nov.), Petalodontiformes (two species), Holocephali (five species), and Euchondrocephali incertae sedis (Cristatodens sigmoidalis gen. et sp. nov.). We also identified primitive polycuspid, clutching teeth representing Phoebodontiformes (Thrinacodus bicuspidatus sp. nov.), Symmoriiformes, and Ctenacanthiformes. The scales are typical growing, compound forms of the protacrodont, ctenacanth, and hybodont types. Two problematic denticulated plates were found, one of which resembles mandibular or palatal plates of Sibyrhynchus (Iniopterygii). Several of the identified chondrichthyan taxa have hitherto been known only from Laurussia, especially from the British Isles and central USA. In particular we found the first record of Chondrenchelyssp. and Diclitodus denshumani outside their type locality. Th. bicuspidatus sp. nov., also known from Nevada, Iran, and NW Australia, appears to be a cosmopolitan, middle Tournaisian index fossil.
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).
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