A large Compsognathid from the early cretaceous Yixian formation of China
By Sunny H. Hwang, M. Norell, Ji Qiang, Gao Ke-Qin. 2004
99 citations recorded by the source corpus.
Subfields: Nature and Landscape Conservation, Paleontology
View Paper: https://www.semanticscholar.org/paper/942b7252f3e8f43e6d2f90c5defe918c2f6323c3
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In Nature and Landscape Conservation
In Paleontology
Citations in the corpus
- The Osteology of Alioramus, A Gracile and Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) from the Late Cretaceous of Mongolia (2012, background): “2), and other basal coelurosaurs (e.g., Huaxiagnathus: Hwang et al., 2004; Juravenator: Gohlich and Chiappe, 2006).”
- MY THEROPOD IS BIGGER THAN YOURS … OR NOT: ESTIMATING BODY SIZE FROM SKULL LENGTH IN THEROPODS (2007, background): “Although the distal portion of the tail is missing, Huaxiagnathus has been assigned a conservative body length estimate of 1.60 m (Hwang et al., 2004).”
- AXIAL SKELETON ONTOGENY IN THE PARASUCHIA (ARCHOSAURIA: PSEUDOSUCHIA) AND ITS IMPLICATIONS FOR ONTOGENETIC DETERMINATION IN ARCHOSAURS (2007, background): “Several examples within the literature suggest that neurocentral suture closure in Theropoda may be useful as an ontogenetic trend (Martill et al., 2000; Ji et al., 2003; Hwang et al., 2004), but no study has explicitly tested this.”
- Osteology of Cryolophosaurus ellioti (Dinosauria: Theropoda) from the Early Jurassic of Antarctica and implications for early theropod evolution (2007, methodology): “’s (2006) analysis of coelurosaurian relationships (note that this represents one of the more recent incarnations of the Theropod Working Group’s character matrix: Norell et al., 2001; Xu et al., 2002; Hwang et al., 2004).”
- The distribution of dental features in non-avian theropod dinosaurs: Taxonomic potential, degree of homoplasy, and major evolutionary trends (2019, background): “…and possibly Juravenator (a single tooth, Rmx8, shows what could be mesial denticles on the crown apex) having also a few lateral teeth with denticles on both carinae (e.g., JME Sch 200; Currie and Chen, 2001; Hwang et al., 2004; Peyer, 2006; Ji et al., 2007; Dal Sasso and Maganuco, 2011).”
- A Review of Dromaeosaurid Systematics and Paravian Phylogeny (2012, methodology): “DISTRIBUTION: Campanian, Djadokhta Formation, Xanadu sublocality, Ukhaa Tolgod, Ömnögov, Mongolia.”
- Phylogeny of Allosauroidea (Dinosauria: Theropoda): Comparative analysis and resolution (2008, background): “While the use of higher-level terminal taxa can be problematic, Compsognathidae is demonstrably monophyletic (Hwang et al. 2004), and codings based on several taxa (Compsognathus, Sinosauropteryx, Huaxiagnathus, and Mirischia) compensate for fragmentary specimens and incomplete illustrations and des”
- Non‐avian dinosaur fossils from the Lower Cretaceous Jehol Group of western Liaoning, China (2006, background): “Hwang et al. (2004) posited this taxon within the Compsognathidae based on a numerical phylogenetic analysis.”
- The Early Evolution of Archosaurs: Relationships and the Origin of Major Clades (2011, result): “24) (Rauhut, 1997, 2003; Hwang et al., 2004; Smith et al., 2007).”
- A juvenile specimen of a new coelurosaur (Dinosauria: Theropoda) from the Middle–Late Jurassic Shishugou Formation of Xinjiang, People's Republic of China (2014, background): “Metacarpal II is mediolaterally wider than the other metacarpals, and its first phalanx has a diameter greater than that of the radius, as in alvarezsauroids (Choiniere et al. 2010b) and compsognathids (Currie & Chen 2001; Hwang et al. 2004; Dal Sasso & Maganuco 2011).”