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Chimaeroid fish

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Journal Article
Published: 01 November 2005
Journal of Paleontology (2005) 79 (6): 1219–1221.
...DENNIS PARMLEY; DAVID J. CICIMURRI Although fossilized teeth of sharks and rays are common elements in Eocene nearshore marine sediments of the southeastern United States ( Parmley and Cicimurri, 2003 and references within), fossil remains of chimaeroid fishes are unknown from this region...
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Sharks and <b>chimaeroid</b> <b>fish</b>. A) Xenacanthus cf. ossiani, oblique lingual vie...
Published: 01 October 2011
FIGURE 7— Sharks and chimaeroid fish. A) Xenacanthus cf. ossiani, oblique lingual view, USNM 542531. B) Xenacanthus cf. ossiani, occlusal view, USNM 542531. C) Elasmobranchii indet., lateral view, USNM 542537. D) Elasmobranchii indet., dorsal view, USNM 542537. E) Orthacanthus cf. compressus
Journal Article
Published: 01 May 1946
Journal of Paleontology (1946) 20 (3): 261–266.
Journal Article
Published: 01 February 2004
Journal of Paleontology (2004) 78 (2): 388–392.
... Mine, Sewell, Mantua Township, Gloucester County, New Jersey, USA. 18 07 2003 The Paleontological Society 2004 T he chimaeroid fishes enter the fossil record in the Triassic, multiply and diversify to at least 16 genera in the later Mesozoic ( Stahl, 1999 ), and then dwindle...
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Figure  14 —Map of biogeographic ranges of all seven fossil leaf species de...
Published: 01 May 2007
of molluscan genera and chimaeroid fish in the Fox Hills Formation of North Dakota (modified from Erickson, 1973 , fig. 3). The white area in North America illustrates area possibly covered by the Fox Hills Sea during the Late Cretaceous. N indicates northern region demonstrated by biogeographic ranges
Journal Article
Journal: PALAIOS
Published: 01 October 2011
PALAIOS (2011) 26 (10): 639–657.
...FIGURE 7— Sharks and chimaeroid fish. A) Xenacanthus cf. ossiani, oblique lingual view, USNM 542531. B) Xenacanthus cf. ossiani, occlusal view, USNM 542531. C) Elasmobranchii indet., lateral view, USNM 542537. D) Elasmobranchii indet., dorsal view, USNM 542537. E) Orthacanthus cf. compressus...
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Journal Article
Published: 01 September 2012
Journal of Paleontology (2012) 86 (5): 886–905.
... and seventh ( Heptranchias ). Fusion of the posteriormost pharyngobranchials also occurs in chimaeroids (e.g., Hydrolagus ), but has not yet been reported in any other chondrichthyan taxa. Jaw musculature has been reconstructed previously in only a few fossil chondrichthyans, including a cladoselachian...
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Journal Article
Published: 01 May 2007
Journal of Paleontology (2007) 81 (3): 550–567.
... of molluscan genera and chimaeroid fish in the Fox Hills Formation of North Dakota (modified from Erickson, 1973 , fig. 3). The white area in North America illustrates area possibly covered by the Fox Hills Sea during the Late Cretaceous. N indicates northern region demonstrated by biogeographic ranges...
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Geographic position and geological section of Beloe Ozero locality. (a) Map...
Published: 03 December 2020
is indicated by arrow. Legend to the section: (1) siliceous clay, (2) siliceous sandstone, (3) silty sand, (4) inequigranular sand, (5) phosphorite nodules, (6) glauconite, (7) bioturbation, (8) thin-walled shells of linguliform brachiopods, (9) scales and bones of small teleostean fishes, including those
Journal Article
Published: 15 July 2009
Geological Magazine (2009) 146 (5): 743–760.
...KATE TRINAJSTIC; JOHN A. LONG Abstract An almost complete but predominantly disarticulated ptyctodont fish, Kimbryanodus williamburyensis n. gen., n.sp. from the Late Devonian Gneudna Formation, is described. The fossils occur as three-dimensionally preserved isolated plates, and this has allowed...
Journal Article
Published: 03 June 2015
Geological Magazine (2016) 153 (1): 1–16.
... between the Early and Late Cretaceous. In addition to ichthyosaur and plesiosaur remains, those of bony fish, lamniform sharks, chimaeroids (Radwański, 1968 ; Marcinowski & Radwański, 1983 ; Popov & Machalski, 2014 ), marine protostegid turtles and pterosaurs...
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Journal Article
Published: 01 May 2014
Journal of Paleontology (2014) 88 (3): 411–420.
... is placed few meters under distinctive levels of glauconite which includes abundant fragments of disarticulated bony fishes near its base. Such lithology, together with the kind of fossils and preservation, was considered indicative of the K/T boundary ( Zinsmeister, 1998 ). The preserved teeth include...
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Journal Article
Published: 01 November 2007
Geological Magazine (2007) 144 (6): 1021–1025.
...–1898) , the vertebrate assemblage from Boca do Chapim, identified mainly on the basis of isolated teeth, included a chimaeroid fish, the purported crocodilian Suchosaurus girardi , the theropod Megalosaurus superbus , the sauropod Pleurocoelus valdensis and the ornithopod Iguanodon mantelli...
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Journal Article
Published: 01 February 2018
Italian Journal of Geosciences (2018) 137 (1): 151–159.
... were represented, to date, by fish teeth from the Erbaense Zone of Mt. La Pelosa (Polino, Terni, Central Italy), referred by M ariotti & S chiavinotto (1977) to Oxyrhina sp. Fig. 1 - A) Location of the study area (black star); B) Structural setting of PCP-basin systems, in black...
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Series: Geological Society, London, Special Publications
Published: 01 January 2016
DOI: 10.1144/SP430.19
EISBN: 9781862399624
.... [Abstract.] Geological Magazine, Decade 3 , 6 , 427–428. 1889 On the Myriacanthidae – an Extinct Family of Chimaeroid Fishes. Annals and Magazine of Natural History, Series 6 , 4 , 275–280. 1889 Preliminary Notes on some new and little-known British Jurassic Fishes. Geological Magazine, Decade 3...
Journal Article
Published: 08 July 2013
Geological Magazine (2014) 151 (3): 517–533.
... accounts of vertebrate remains from this locality; an early exception is the report of fish remains by Bolton ( 1889 ) who described coelacanth and indeterminate fish bones from a locality east of Bacup and an occurrence of Listracanthus in shales above the Bullion Coal, also at Bacup...
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Journal Article
Published: 01 July 2014
Journal of Paleontology (2014) 88 (4): 636–651.
... to generate endocast models for the Paleozoic actinopterygian fishes Mimipiscis and Kentuckia , which serve as key representatives of anatomically primitive, early ray fins in analyses of early vertebrate relationships. The resultant endocranial models generally corroborate existing accounts of endocranial...
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Journal Article
Published: 01 December 2018
Journal of Paleontology (2018) 92 (S77): 1–33.
... localities within the Grand Canyon have produced identifiable vertebrate fossils from the Surprise Canyon and Watahomigi formations ( Fig. 1 ). However, of these eight localities, only four show significant fish assemblages from the transitional lower/middle, middle, and upper members of the Surprise Canyon...
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Journal Article
Published: 08 May 2018
Journal of the Geological Society (2018) 175 (4): 569–579.
...Matt Friedman; Giorgio Carnevale Abstract The Eocene limestones around the Italian village of Bolca occur in a series of distinct localities providing a unique snapshot of marine life in the early Cenozoic. Famous for its fishes, the localities of Bolca also yield diverse invertebrate faunas...
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Journal Article
Journal: PALAIOS
Published: 01 November 2014
PALAIOS (2014) 29 (11): 560–569.
.... Buscalioni A.D. Guerrero M.C. 2013 , Involvement of microbial mats in delayed decay: an experimental essay on fish preservation : PALAIOS , v. 28 , p. 56 – 66 , doi: 10.2110/Palo.2011.P11-099r...
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