The Distinctive Theropod Assemblage of the Ellisdale Site of New Jersey and Its Implications for North American Dinosaur Ecology and Evolution During the Cretaceous
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New Tyrannosaur from the Mid-Cretaceous of Uzbekistan Clarifies Evolution of Giant Body Sizes and Advanced Senses in Tyrant Dinosaurs
Edinburgh Research Explorer New tyrannosaur from the mid-Cretaceous of Uzbekistan clarifies evolution of giant body sizes and advanced senses in tyrant dinosaurs Citation for published version: Brusatte, SL, Averianov, A, Sues, H, Muir, A & Butler, IB 2016, 'New tyrannosaur from the mid-Cretaceous of Uzbekistan clarifies evolution of giant body sizes and advanced senses in tyrant dinosaurs', Proceedings of the National Academy of Sciences, pp. 201600140. https://doi.org/10.1073/pnas.1600140113 Digital Object Identifier (DOI): 10.1073/pnas.1600140113 Link: Link to publication record in Edinburgh Research Explorer Document Version: Peer reviewed version Published In: Proceedings of the National Academy of Sciences General rights Copyright for the publications made accessible via the Edinburgh Research Explorer is retained by the author(s) and / or other copyright owners and it is a condition of accessing these publications that users recognise and abide by the legal requirements associated with these rights. Take down policy The University of Edinburgh has made every reasonable effort to ensure that Edinburgh Research Explorer content complies with UK legislation. If you believe that the public display of this file breaches copyright please contact [email protected] providing details, and we will remove access to the work immediately and investigate your claim. Download date: 04. Oct. 2021 Classification: Physical Sciences: Earth, Atmospheric, and Planetary Sciences; Biological Sciences: Evolution New tyrannosaur from the mid-Cretaceous of Uzbekistan clarifies evolution of giant body sizes and advanced senses in tyrant dinosaurs Stephen L. Brusattea,1, Alexander Averianovb,c, Hans-Dieter Suesd, Amy Muir1, Ian B. Butler1 aSchool of GeoSciences, University of Edinburgh, Edinburgh EH9 3FE, UK bZoological Institute, Russian Academy of Sciences, St. -
A New Caenagnathid Dinosaur from the Upper Cretaceous Wangshi
www.nature.com/scientificreports OPEN A new caenagnathid dinosaur from the Upper Cretaceous Wangshi Group of Shandong, China, with Received: 12 October 2017 Accepted: 7 March 2018 comments on size variation among Published: xx xx xxxx oviraptorosaurs Yilun Yu1, Kebai Wang2, Shuqing Chen2, Corwin Sullivan3,4, Shuo Wang 5,6, Peiye Wang2 & Xing Xu7 The bone-beds of the Upper Cretaceous Wangshi Group in Zhucheng, Shandong, China are rich in fossil remains of the gigantic hadrosaurid Shantungosaurus. Here we report a new oviraptorosaur, Anomalipes zhaoi gen. et sp. nov., based on a recently collected specimen comprising a partial left hindlimb from the Kugou Locality in Zhucheng. This specimen’s systematic position was assessed by three numerical cladistic analyses based on recently published theropod phylogenetic datasets, with the inclusion of several new characters. Anomalipes zhaoi difers from other known caenagnathids in having a unique combination of features: femoral head anteroposteriorly narrow and with signifcant posterior orientation; accessory trochanter low and confuent with lesser trochanter; lateral ridge present on femoral lateral surface; weak fourth trochanter present; metatarsal III with triangular proximal articular surface, prominent anterior fange near proximal end, highly asymmetrical hemicondyles, and longitudinal groove on distal articular surface; and ungual of pedal digit II with lateral collateral groove deeper and more dorsally located than medial groove. The holotype of Anomalipes zhaoi is smaller than is typical for Caenagnathidae but larger than is typical for the other major oviraptorosaurian subclade, Oviraptoridae. Size comparisons among oviraptorisaurians show that the Caenagnathidae vary much more widely in size than the Oviraptoridae. Oviraptorosauria is a clade of maniraptoran theropod dinosaurs characterized by a short, high skull, long neck and short tail. -
New Oviraptorid Dinosaur (Dinosauria: Oviraptorosauria) from the Nemegt Formation of Southwestern Mongolia
Bull. Natn. Sci. Mus., Tokyo, Ser. C, 30, pp. 95–130, December 22, 2004 New Oviraptorid Dinosaur (Dinosauria: Oviraptorosauria) from the Nemegt Formation of Southwestern Mongolia Junchang Lü1, Yukimitsu Tomida2, Yoichi Azuma3, Zhiming Dong4 and Yuong-Nam Lee5 1 Institute of Geology, Chinese Academy of Geological Sciences, Beijing 100037, China 2 National Science Museum, 3–23–1 Hyakunincho, Shinjukuku, Tokyo 169–0073, Japan 3 Fukui Prefectural Dinosaur Museum, 51–11 Terao, Muroko, Katsuyama 911–8601, Japan 4 Institute of Paleontology and Paleoanthropology, Chinese Academy of Sciences, Beijing 100044, China 5 Korea Institute of Geoscience and Mineral Resources, Geology & Geoinformation Division, 30 Gajeong-dong, Yuseong-gu, Daejeon 305–350, South Korea Abstract Nemegtia barsboldi gen. et sp. nov. here described is a new oviraptorid dinosaur from the Late Cretaceous (mid-Maastrichtian) Nemegt Formation of southwestern Mongolia. It differs from other oviraptorids in the skull having a well-developed crest, the anterior margin of which is nearly vertical, and the dorsal margin of the skull and the anterior margin of the crest form nearly 90°; the nasal process of the premaxilla being less exposed on the dorsal surface of the skull than those in other known oviraptorids; the length of the frontal being approximately one fourth that of the parietal along the midline of the skull. Phylogenetic analysis shows that Nemegtia barsboldi is more closely related to Citipati osmolskae than to any other oviraptorosaurs. Key words : Nemegt Basin, Mongolia, Nemegt Formation, Late Cretaceous, Oviraptorosauria, Nemegtia. dae, and Caudipterygidae (Barsbold, 1976; Stern- Introduction berg, 1940; Currie, 2000; Clark et al., 2001; Ji et Oviraptorosaurs are generally regarded as non- al., 1998; Zhou and Wang, 2000; Zhou et al., avian theropod dinosaurs (Osborn, 1924; Bars- 2000). -
Note on the Sauropod and Theropod Dinosaurs from the Upper Cretaceous of Madagascar*
EXTRACT FROM THE BULLETIN DE LA SOCIÉTÉ GÉOLOGIQUE DE FRANCE 3rd series, volume XXIV, page 176, 1896. NOTE ON THE SAUROPOD AND THEROPOD DINOSAURS FROM THE UPPER CRETACEOUS OF MADAGASCAR* by Charles DEPÉRET. (PLATE VI). Translated by Matthew Carrano Department of Anatomical Sciences SUNY at Stony Brook, September 1999 The bones of large dinosaurian reptiles described in this work were brought to me by my good friend, Mr. Dr. Félix Salètes, primary physician for the Madagascar expedition, from the environs of Maevarana, where he was charged with installing a provisional hospital. This locality is situated on the right bank of the eastern arm of the Betsiboka, 46 kilometers south of Majunga, on the northwest coast of the island of Madagascar. Not having the time to occupy himself with paleontological studies, Dr. Salètes charged one of his auxiliary agents, Mr. Landillon, company sergeant-major of the marines, with researching the fossils in the environs of the Maevarana post. Thanks to the zeal and activity of Mr. Landillon, who was not afraid to gravely expose his health in these researches, I have been able to receive the precious bones of terrestrial reptiles that are the object of this note, along with an important series of fossil marine shells. I eagerly seize the opportunity here to thank Mr. Landillon for his important shipment and for the very precise geological data which he communicated to me concerning the environs of Maevarana, and of which I will now give a short sketch. 1st. Geology of Maevarana and placement of the localities. * Original reference: Depéret, C. -
1 JOURNAL of VERTEBRATE PALEONTOLOGY a New
JOURNAL OF VERTEBRATE PALEONTOLOGY A new caenagnathid (Dinosauria: Oviraptorosauria) from the Horseshoe Canyon Formation of Alberta, Canada, and a reevaluation of the relationships of Caenagnathidae GREGORY F. FUNSTON*,,PHILIP J. CURRIE Department of Biological Sciences, CW 405, Biological Sciences Building, University of Alberta,Edmonton, Alberta, Canada T6G 2E9 [email protected]; [email protected] SUPPLEMENTARY DATA 1 1 CHARACTERS MODIFIED FROM LAMANNA ET AL. (2014) 78. Dentary: (0) elongate; (1) proportionally short and deep, with maximum depth of dentary between 25% and 50% of dentary length (with length measured from the tip of the jaw to the end of the posterodorsal process); (2) extremely short and deep, with maximum depth 50% or more of dentary length. [ORDERED] Modification—Removed [ORDERED] Justification—Mandibular variation through ontogeny in has not been qualified in oviraptorosaurs, nor has the degree of intraspecific variation. This character in particular is correlated with size in caenagnathids, such that larger specimens tend show state 0, and smaller specimens tend to show state 2, with a smooth gradient between. 84. Anterodorsal margin of dentary in lateral view: (0) straight; (1) concave; (2) broadly concave. [ORDERED] Modification—Removed [ORDERED] Justification—As above, though the opposite correlation to size is shown: large specimens tend to show state 2, and small specimens tend to show state 0. 176. Manual phalanx II-2: (0) longer than II-1; (1) subequal to or slightly shorter than II- 1; (2) distinctly shorter than II-1. [ORDERED] Modification—Removed [ORDERED] Justification—Caenagnathid manual proportions are highly variable, with a number of apparent reversals within clades. For example, Hagryphus giganteus, scored as character state 1 for this character, is consistently recovered as a basal caenagnathid, but within more derived caenagnathids, all three character states for this character are present, indicating that the character state can move both directions. -
Index of Subjects
Cambridge University Press 978-1-108-47594-5 — Dinosaurs 4th Edition Index More Information INDEX OF SUBJECTS – – – A Zuul, 275 276 Barrett, Paul, 98, 335 336, 406, 446 447 Ankylosauridae Barrick, R, 383–384 acetabulum, 71, 487 characteristics of, 271–273 basal dinosauromorph, 101 acromial process, 271, 273, 487 cladogram of, 281 basal Iguanodontia, 337 actual diversity, 398 defined, 488 basal Ornithopoda, 336 adenosine diphosphate, see ADP evolution of, 279 Bates, K. T., 236, 360 adenosine triphosphate, see ATP ankylosaurids, 275–276 beak, 489 ADP (adenosine diphosphate), 390, 487 anpsids, 76 belief systems, 474, 489 advanced characters, 55, 487 antediluvian period, 422, 488 Bell, P. R., 162 aerobic metabolism, 391, 487 anterior position, 488 bennettitaleans, 403, 489 – age determination (dinosaur), 354 357 antorbital fenestra, 80, 488 benthic organisms, 464, 489 Age of Dinosaurs, 204, 404–405 Arbour, Victoria, 277 Benton, M. J., 2, 104, 144, 395, 402–403, akinetic movement, see kinetic movement Archibald, J. D., 467, 469 444–445, 477–478 Alexander, R. M., 361 Archosauria, 80, 88–90, 203, 488 Berman, D. S, 236–237 allometry, 351, 487 Archosauromorpha, 79–81, 488 Beurien, Karl, 435 altricial offspring, 230, 487 archosauromorphs, 401 bidirectional respiration, 350 Alvarez, Luis, 455 archosaurs, 203, 401 Big Al, 142 – Alvarez, Walter, 442, 454 455, 481 artifacts, 395 biogeography, 313, 489 Alvarezsauridae, 487 Asaro, Frank, 455 biomass, 415, 489 – alvarezsaurs, 168 169 ascending process of the astragalus, 488 biosphere, 2 alveolus/alveoli, -
Nanotyrannus’ As a Valid Taxon Of
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Queen Mary Research Online Dentary groove morphology does not distinguish ‘Nanotyrannus’ as a valid taxon of tyrannosauroid dinosaur. Comment on: “Distribution of the dentary groove of theropod dinosaurs: implications for theropod phylogeny and the validity of the genus Nanotyrannus Bakker et al., 1988” Stephen L. Brusatte1*, Thomas D. Carr2, Thomas E. Williamson3, Thomas R. Holtz, Jr.4,5, David W. E. Hone6, Scott A. Williams7 1 School of GeoSciences, University of Edinburgh, Grant Institute, James Hutton Road, Edinburgh, EH9 3FE, United Kingdom, [email protected] 2Department of Biology, Carthage College, 2001 Alford Park Drive, Kenosha, WI 53140, USA 3New Mexico Museum of Natural History and Science, 1801 Mountain Road, NW, Albuquerque, NM 87104, USA 4Department of Geology, University of Maryland, 8000 Regents Drive, College Park, MD 20742, USA 5Department of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560, USA 6School of Biological and Chemical Sciences, Queen Mary University of London, Mile End Road, London, E1 4NS, United Kingdom. 7Burpee Museum of Natural History, 737 North Main Street, Rockford, IL 60115, USA *Corresponding author ABSTRACT: There has been considerable debate about whether the controversial tyrannosauroid dinosaur ‘Nanotyrannus lancensis’ from the uppermost Cretaceous of North America is a valid taxon or a juvenile of the contemporaneous Tyrannosaurus rex. In a recent Cretaceous Research article, Schmerge and Rothschild (2016) brought a new piece of evidence to this discussion: the morphology of the dentary groove, a depression on the lateral surface of the dentary that houses neurovascular foramina. -
Limb Design, Function and Running Performance in Ostrich-Mimics and Tyrannosaurs
GAIA Nº 15, LISBOA/LISBON, DEZEMBRO/DECEMBER 1998, pp. 257-270 (ISSN: 0871-5424) LIMB DESIGN, FUNCTION AND RUNNING PERFORMANCE IN OSTRICH-MIMICS AND TYRANNOSAURS Gregory S. PAUL 3109 N Calvert St. Side Apt., BALTIMORE MD 21218. USA ABSTRACT: Examination of the limb morphology of small ornithomimids and large tyranno- saurids shows that they remained remarkably constant in design regardless of size. The changes that were present were consistent with maintaining limb strength and function constant with size. It is concluded that ornithomimid and tyrannosaurid legs functioned in a similar manner, and always exhibit the features normally associated with a fast running gait. This is in contrast to modern animals, in which elephants as gigantic as large tyranno- saurids have limbs that are modified for a slow walking gait. INTRODUCTION to run observed in elephants. The hypothesis can be challenged if it can be shown that at least some ex- Because they had long, gracile, bird-like legs, it tinct giants retained the skeletal adaptations for run- has long been accepted that the smaller predatory ning observed in smaller species, and in their own dinosaurs were swift runners (O [& GREG- SBORN offspring. In turn, the hypothesis that giants can run ], 1916; COLBERT, 1961; RUSSELL, 1972; ORY fast if they retain limbs similar to smaller runners can C , 1978; THULBORN, 1982; PAUL, 1988; OOMBS be challenged if it is shown that the skeleton is too H , 1994). Much more controversial has been OLTZ vulnerable to structural failure. the locomotory abilities of their giant relatives, which have been restored as no faster than elephants BODY MASSES (LAMBE, 1917; HALSTEAD &HALSTEAD, 1981; THUL- BORN, 1982; BARSBOLD, 1983), able to run at only Sources for mass data for extinct and extant ani- modest speeds (COOMBS, 1978; MOLNAR &FAR- mals include PAUL (1988, 1997), NOWAK (1991) and LOW, 1990; HORNER &LESSEM, 1993; FARLOW, MATTHEWS (1994). -
New Tyrannosaur from the Mid-Cretaceous of Uzbekistan Clarifies Evolution of Giant Body Sizes and Advanced Senses in Tyrant Dinosaurs
New tyrannosaur from the mid-Cretaceous of Uzbekistan clarifies evolution of giant body sizes and advanced senses in tyrant dinosaurs Stephen L. Brusattea,1, Alexander Averianovb,c, Hans-Dieter Suesd, Amy Muira, and Ian B. Butlera aSchool of GeoSciences, University of Edinburgh, Edinburgh EH9 3FE, United Kingdom; bZoological Institute, Russian Academy of Sciences, St. Petersburg 199034, Russia; cDepartment of Sedimentary Geology, Saint Petersburg State University, St. Petersburg 199178, Russia; and dDepartment of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560 Edited by Neil H. Shubin, The University of Chicago, Chicago, IL, and approved January 29, 2016 (received for review January 5, 2016) Tyrannosaurids—the familiar group of carnivorous dinosaurs in- We here report the first diagnostic tyrannosauroid from the mid- cluding Tyrannosaurus and Albertosaurus—were the apex predators Cretaceous, a new species from the Turonian (ca. 90–92 million in continental ecosystems in Asia and North America during the years ago) Bissekty Formation of Uzbekistan. This formation has latest Cretaceous (ca. 80–66 million years ago). Their colossal sizes recently emerged as one of the most important records of mid- and keen senses are considered key to their evolutionary and eco- Cretaceous dinosaurs globally (9–11). Possible tyrannosauroid logical success, but little is known about how these features devel- specimens from the Bissekty Formation were reported more than oped as tyrannosaurids evolved from smaller basal tyrannosauroids a half century ago (12), and, more recently, several isolated fossils that first appeared in the fossil record in the Middle Jurassic (ca. 170 were assigned to the group (9, 13), but none of these has been million years ago). -
Body-Size Evolution in the Dinosauria
8 Body-Size Evolution in the Dinosauria Matthew T. Carrano Introduction The evolution of body size and its influence on organismal biology have received scientific attention since the earliest decades of evolutionary study (e.g., Cope, 1887, 1896; Thompson, 1917). Both paleontologists and neontologists have attempted to determine correlations between body size and numerous aspects of life history, with the ultimate goal of docu- menting both the predictive and causal connections involved (LaBarbera, 1986, 1989). These studies have generated an appreciation for the thor- oughgoing interrelationships between body size and nearly every sig- nificant facet of organismal biology, including metabolism (Lindstedt & Calder, 1981; Schmidt-Nielsen, 1984; McNab, 1989), population ecology (Damuth, 1981; Juanes, 1986; Gittleman & Purvis, 1998), locomotion (Mc- Mahon, 1975; Biewener, 1989; Alexander, 1996), and reproduction (Alex- ander, 1996). An enduring focus of these studies has been Cope’s Rule, the notion that body size tends to increase over time within lineages (Kurtén, 1953; Stanley, 1973; Polly, 1998). Such an observation has been made regarding many different clades but has been examined specifically in only a few (MacFadden, 1986; Arnold et al., 1995; Jablonski, 1996, 1997; Trammer & Kaim, 1997, 1999; Alroy, 1998). The discordant results of such analyses have underscored two points: (1) Cope’s Rule does not apply universally to all groups; and (2) even when present, size increases in different clades may reflect very different underlying processes. Thus, the question, “does Cope’s Rule exist?” is better parsed into two questions: “to which groups does Cope’s Rule apply?” and “what process is responsible for it in each?” Several recent works (McShea, 1994, 2000; Jablonski, 1997; Alroy, 1998, 2000a, 2000b) have begun to address these more specific questions, attempting to quantify patterns of body-size evolution in a phylogenetic (rather than strictly temporal) context, as well as developing methods for interpreting the resultant patterns. -
Ornithomimids from the Nemegt Formation of Mongolia
J. Paleont. Soc. Korea. Vol. 22, No. 1, (2006) : p. 195-207 ORNITHOMIMIDS FROM THE NEMEGT FORMATION OF MONGOLIA Yoshitsugu Kobayashi1 and Rinchen Barsbold2 1Hokkaido University Museum, Hokkaido University, Sapporo, Hokkaido, 060-0810 Japan, [email protected] 2Paleontological Center of Mongolian Academy of Sciences, PO Box 260, Ulaan Bataar 210351, Mongolia, [email protected] Abstract: Two ornithomimids (Gallimimus bullatus and Anserimimus planinychus) and an enigmatic ornithomi- mid (Deinocheirus mirificus) from the Nemegt Formation (Maastrichtian) of Mongolia are reviewed in this study. Gallimimus bullatus is one of the best-known ornithomimids, but its diagnoses need to be revised. The length ratio of the manus/humerus in Gallimimus bullatusis 0.61. This is the smallest value in ornithomimosaurs (approximately 0.8 or more in other ornithomimosaurs) and may be a good character to diagnose Gallimimus bullatus as suggested by previous studies. Anserimimus planinychus is a unique ornithomimosaur in having strong deltopectoral crest of the humerus, dorsoventrally flat and nearly straight manual unguals, and long forelimbs. Anserimimus planinychus shares two characters (position of the biceps tubercle and alignment of the glenoid) with Gallimimus bullatus and has a long metacarpal I as in Ornithomimus edmontonicus (derived ornithomimosaur) and a long metacarpal III as in Harpymimus okladnikovi (primitive ornithomimosaur). The phylogenetic position of Deinocheirus mirificus has been problematic since its discovery. Preliminary -
Dinosaurs Found in Utah Record Chart
UTAH’S DINOSAUR RECORD GEOLOGIC UTAH’S MESOZOIC TIME SCALE ROCK RECORD Southern Tyrannosaurus Torosaurus & Alamosaurus fauna Tyrannosaurus Alamosaurus ankylosaurid teeth long-horned 65 NORTH HORN FORMATION centrosaurines Maastrichtian Ornithomimus new chasmosaurines Hagryphus DINOSAUR Highest diversity North America ceratopsid & KAIPAROWITS FORMATION hadrosaurid fauna Gryposaurus Edmontonia EXTINCTION 75 Campanian new tyrannosaurids Parasaurolophus new tyrannosaurid First centrosaurines Diabloceratops WAHWEAP FORMATION - MASUK FORMATION & hadrosaurids new hadrosaurine pachycephalosaurs nodosaurids Santonian Upper STRAIGHT CLIFFS FORMATION Diverse tooth fauna Blue Gate Member MANCOS SHALE First ceratopsomorphs Coniacian Zuniceratops advanced nodosaurid National Monument Ferron Sandstone - Smoky Hollow Member Nothronychus hadrosauromorphs teeth Turonian Local extinction Pachycephalosaurid TROPIC SHALE. - Tununk Member MANCOS SHALE of sauropods Grand Sraircase - Escalante teeth ornithomimid DAKOTA FORMATION Asian immigration tiny Cenomanian ornithopod Eolambia Mussentuchit Member induced extinction tyrannosaurid and origin of North teeth tiny pleurocoelid 100 troodontid teeth American Late neoceratopsian teeth Animantarx brachiosaurid teeth Cretaceous dinosaur Albian fauna Ruby Ranch Cedarpelta Member Isolation of North Tennontosaurus nodosaurids America resulting Abydosaurus in local extinctions pleurocoelid Deinonychus and increased Acrocanthosaurus brachiosaurids Aptian FORMATION endemism Nedcolbertia new camarasaurid Poison Strip Sandstone