Regular ArticleThe evolution of pelvic osteology and soft tissues on the line to extant birds (Neornithes)
By John R. Hutchinson. 2001
108 citations recorded by the source corpus.
Subfields: Nature and Landscape Conservation, Paleontology
View Paper: https://www.semanticscholar.org/paper/8b94e9a3959d9f7d0171fb853765028d9043ddf8
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In Nature and Landscape Conservation
In Paleontology
Citations in the corpus
- Postcranial Anatomy of Sebecus icaeorhinus (Crocodyliformes, Sebecidae) from the Eocene of Patagonia (2012, background): “The morphology of the insertion area of PIFI1 is markedly different from that of other basal mesoeucrocodylians (except for Iberosuchus), in which the depression is deeper and its anterior border extends as a pronounced flange with a concave proximal margin (e.g., Araripesuchus, Notosuchus, Simosuch”
- Baurusuchid crocodyliforms as theropod mimics: clues from the skull and appendicular morphology of Stratiotosuchus maxhechti (Upper Cretaceous of Brazil) (2011, background): “The phylogenetic position of the Pakistani form as a baurusuchid is not consensual, being supported by Turner (2006) but not by Larsson & Sues (2007), who included Pabwehshi as more closely related to Sebecus and to the Peirosauridae in the clade Sebecia, which excludes the Baurusuchidae.”
- The Late Triassic dinosauromorph Sacisaurus agudoensis (Caturrita Formation; Rio Grande do Sul, Brazil): anatomy and affinities (2013, background): “The second forms a proximodistally elongated ‘pubic tubercle’ (sensu Hutchinson 2001), continues distally as the lateral margin of the shaft, but is proximally bifurcated into two branches at the level Fig.”
- New Specimens of Microraptor zhaoianus (Theropoda: Dromaeosauridae) from Northeastern China (2002, unknown): “A vertical ridge dividing the anterior and posterior portions of the ilium, as seen in some Velociraptor specimens (IGM 100-1982; see Norell and Makovicky, 1999) and many other theropods (Hutchinson, 2001), is not present.”
- Osteology and relationships of a new theropod dinosaur from the Middle Jurassic of Patagonia (2005, background): “Just above the distal condyles, the adductor ridge (Hutchinson 2001b) is developed on the posterior side as a broadly rounded, low and slightly rugose ridge that extends from the distal posteromedial edge proximolaterally (Textfig.”
- The Locomotor Musculature of Basal Ornithischian Dinosaurs (2011, background): “The pubis of ornithischians has rotated backwards relative to the primitive condition (described in Hutchinson, 2001a) to lie under the ischium (Fig.”
- A large Compsognathid from the early cretaceous Yixian formation of China (2004, background): “A prominent, triangular obturator process is positioned proximally on the ischium, just distal to the pubic process, as in other less derived coelurosaurs and tetanurans (Hutchinson 2001).”
- Vertebral pneumaticity, air sacs, and the physiology of sauropod dinosaurs (2003, result): “Diaphragmatically driven respiratory systems have been postulated for some theropods (Ruben et al. 1999), but this hypothesis lacks empirical support and is contradicted by several lines of evidence (Claessens et al. 1998; Christiansen and Bonde 2000; Hutchinson 2001; Padian 2001).”
- An integrative phylogenetic and extrapolatory approach to the reconstruction of dromaeosaur (Theropoda: Eumaniraptora) shoulder musculature (2006, background): “…Journal of the Linnean Society, 2006, 146 , 301–344 on bones in three ways: (1) as pits or rugose scars due to tendinous (Hutchinson, 2001b) or aponeurotic (Bryant & Seymour, 1990) attachments; (2) as crests; or (3) as smooth bone surfaces due to fleshy (direct) attachments (Hutchinson, 2001b).”
- The Appendicular Skeleton of Neuquensaurus, a Late Cretaceous Saltasaurine Sauropod from Patagonia, Argentina (2010, background): “—The ischial tuberosity is an ancestral feature present in basal Reptilia (Hutchinson 2001a).”