2003
DOI: 10.1017/s1477201903001032
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Osteology and phylogeny ofZalmoxes(n. g.), an unusual Euornithopod dinosaur from the latest Cretaceous of Romania

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Cited by 173 publications
(426 citation statements)
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References 46 publications
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“…Analysed clades include: non-avian coelurosaurian theropods 28 , tyrannosauroid theropods 29 , pachycephalosaurs 30 , ceratopsids (most of which are chasmosaurines, because there is no available global phylogeny of ceratopsids that includes comprehensive sampling of centrosaurines and chasmosaurines 31 ), hadrosauroids 32 , sauropods 33 , and ankylosaurs 34 . Other groups, such as abelisauroid theropods, non-hadrosauroid ornithopods, and non-ceratopsid ceratopsians, could not be analysed because large samples of reasonably complete CampanianMaastrichtian specimens scored for discrete character data are not yet available, almost entirely due to poor fossil sampling [41][42][43] . Birds were not included in the coelurosaur dataset, because we chose to focus specifically on non-avian dinosaurs, and more importantly, because of severe sampling biases that limit the number of Maastrichtian specimens that can be scored for large numbers of discrete characters 44,45 .…”
Section: Methodsmentioning
confidence: 99%
“…Analysed clades include: non-avian coelurosaurian theropods 28 , tyrannosauroid theropods 29 , pachycephalosaurs 30 , ceratopsids (most of which are chasmosaurines, because there is no available global phylogeny of ceratopsids that includes comprehensive sampling of centrosaurines and chasmosaurines 31 ), hadrosauroids 32 , sauropods 33 , and ankylosaurs 34 . Other groups, such as abelisauroid theropods, non-hadrosauroid ornithopods, and non-ceratopsid ceratopsians, could not be analysed because large samples of reasonably complete CampanianMaastrichtian specimens scored for discrete character data are not yet available, almost entirely due to poor fossil sampling [41][42][43] . Birds were not included in the coelurosaur dataset, because we chose to focus specifically on non-avian dinosaurs, and more importantly, because of severe sampling biases that limit the number of Maastrichtian specimens that can be scored for large numbers of discrete characters 44,45 .…”
Section: Methodsmentioning
confidence: 99%
“…The other two reversions, in Ceratopsia and Hadrosauriformes, happened much later in time, during the late Early to early Late Cretaceous (Sereno 1999;Weishampel et al 2004). Another possible independent reversion also occurred in rhabdodontid ornithopods, although the time that this occurred is unclear due to the extensive ghost lineage separating this clade from other ornithopods (Weishampel et al 2003;Maidment and Barrett 2014). It is also possible that the nearest outgroup to Dinosauria, Silesauridae, reverted to quadrupedalism from a bipedal ancestry sometime during the Middle Triassic, but a lack of articulated material makes this claim harder to assess (Langer et al 2013).…”
Section: Introductionmentioning
confidence: 99%
“…5D). This condition appears to be absent in Kangnasaurus (although on the basis of fragmentary material : Cooper, 1985) and is absent in noniguanodontian ornithopods like Hypsilophodon (NHMUK OR28707; NHMUK PV R196), Tenontosaurus (Forster, 1990), rhabdodontids (Weishampel et al, 2003) and ankylopollexians (Norman, 1986). It is difficult to assess this character in Dryosaurus due to damage, but the orientation of the preserved bases of the neural spines suggests that they might have been more vertically inclined and thus might not have extended beyond the posterior margin of the succeeding vertebra (Galton, 1981).…”
Section: Discussionmentioning
confidence: 99%