2013
DOI: 10.4202/app.2013.0018
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A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications

Abstract: Central Asia is a key area for crocodylomorph evolution, lying midway between the highly documented deposits in Europe and

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Cited by 9 publications
(8 citation statements)
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“…However this may be, the biogeographic pattern presented above might furthermore be mirrored by goniopholid crocodiles [ 65 ] and some pterosaur clades [ 66 ], which also seem to have expanded their range from eastern Asia towards Europe in the Late Jurassic. Palaeogeographic reconstructions indicate that at least a narrow marine barrier, probably with numerous islands, existed between Asia and Europe up to the Tithonian, when these landmasses might have been joined [ 67 ].…”
Section: Discussionmentioning
confidence: 99%
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“…However this may be, the biogeographic pattern presented above might furthermore be mirrored by goniopholid crocodiles [ 65 ] and some pterosaur clades [ 66 ], which also seem to have expanded their range from eastern Asia towards Europe in the Late Jurassic. Palaeogeographic reconstructions indicate that at least a narrow marine barrier, probably with numerous islands, existed between Asia and Europe up to the Tithonian, when these landmasses might have been joined [ 67 ].…”
Section: Discussionmentioning
confidence: 99%
“…Palaeogeographic reconstructions indicate that at least a narrow marine barrier, probably with numerous islands, existed between Asia and Europe up to the Tithonian, when these landmasses might have been joined [ 67 ]. Whereas for crocodiles, different tolerances to brackish or even marine waters were evoked to explain the ability to cross the still remaining marine barrier through island hopping [ 65 ], flight ability was probably the key factor in the biogeographical evolution of pterosaurs [ 66 ]. For maniraptorans, small body size of the taxa at the base of all major lineages [ 68 ] might have made oversea dispersal by rafting possible [ 69 ], thus facilitating the crossing of the epicontinental barriers between Asia and Europe.…”
Section: Discussionmentioning
confidence: 99%
“…The second parsimony analysis presented here employs the mA matrix: a modified version of the character and taxon list first published by Andrade et al (2011) , which originally included 104 OTUs scored for 486 characters. As per the recommendations of Andrade et al (2011) , Halliday et al (2015) , and Puértolas-Pascual, Canudo & Sender (2015) , the putative goniopholidid Denazinosuchus kirtlandicus ( Lucas & Sullivan, 2003 ), and the Asian taxon ‘ Goniopholis ’ phuwiangensis Buffetaut & Ingavat, 1983 OTUs, along with the composite ‘ Goniopholis ’ phuwiangensis + Siamosuchus terminal (ALT Siamosuchus ), were excluded due to their instability and, in the case of the latter, inapplicability. Following Halliday et al (2015) and Ristevski et al (2018) the putative goniopholidids Kansajasuchus extensus Efimov, 1975 , Sunosuchus shartegensis Efimov, 1988 and Turanosuchus aralensis Efimov, 1988 were excluded due to their instability.…”
Section: Phylogenetic Analysesmentioning
confidence: 99%
“…In other atoposaurids, this margin, comprising the lateral edge of the postorbital and squamosal, is straight, similar to T. guimarotae (Schwarz & Salisbury, ) and T. pusillus . (S8) External mandibular fenestra present (C207.1) and oval‐shaped with anteroposteriorly orientated long axis (C210.0) : The presence of an external mandibular fenestra is also shared with T. guimarotae (Schwarz & Salisbury, ) amongst those taxa included in our analysis as putative atoposaurids, but also represents the plesiomorphic crocodyliform condition, being present in goniopholidids (e.g. Halliday et al ., ), Protosuchus (Colbert & Mook, ), as well as in notosuchians such as Baurusuchus (Nascimento & Zaher, ) and Labidiosuchus (Kellner et al ., ), in which the opening is enlarged. This fenestra is lost in some advanced neosuchians, including paralligatorids (Montefeltro et al ., ), but is present in most eusuchians and Crocodylia (Brochu, ; Salisbury et al ., ; Pol et al ., ), although in some cases it is strongly reduced (Brochu et al ., ). (S9*) Individual dorsal and caudal osteoderms with unsculpted edges (C304.1), square‐shaped (C308.3), and lacking a dorsal keel anteriorly (C311.0) and posteriorly (C312.0) : The individual osteoderms preserved in Alligatorium meyeri have unsculpted edges on all but the nuchal‐most elements, a feature that cannot be a preservation artefact as the cranial table remains sculpted, and the centre of each osteoderm remains relatively lightly sculpted.…”
Section: Systematic Palaeontologymentioning
confidence: 99%