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Dino Hunt Checklist Card Name Type Rarity Acanthopholis
Dino Hunt Checklist Card Name Type Rarity Acanthopholis Dinosaur Common Acrocanthosaurus Dinosaur Rare Albertosaurus Dinosaur Rare Albertosaurus Dinosaur Ultra Rare Alioramus Dinosaur Rare Allosaurus Dinosaur Rare* Altispinax Dinosaur Rare* Amargasaurus Dinosaur Uncommon* Ammosaurus Dinosaur Uncommon* Anatotitan Dinosaur Common Anchiceratops Dinosaur Common Anchisaurus Dinosaur Common* Ankylosaurus Dinosaur Uncommon* Antarctosaurus Dinosaur Common Apatosaurus Dinosaur Uncommon* Archaeopteryx Dinosaur Rare* Archelon Dinosaur Rare Arrhinoceratops Dinosaur Common Avimimus Dinosaur Common Baby Ankylosaur Dinosaur Common Baby Ceratopsian Dinosaur Common Baby Hadrosaur Dinosaur Common Baby Raptor Dinosaur Rare Baby Sauropod Dinosaur Common Baby Theropod Dinosaur Rare Barosaurus Dinosaur Uncommon Baryonyx Dinosaur Rare* Bellusaurus Dinosaur Common Brachiosaurus Dinosaur Rare* Brachyceratops Dinosaur Uncommon Camarasaurus Dinosaur Common Camarasaurus Dinosaur Ultra Rare Camptosaurus Dinosaur Common Carnotaurus Dinosaur Rare Centrosaurus Dinosaur Common Ceratosaurus Dinosaur Rare* Cetiosaurus Dinosaur Common* Changdusaurus Dinosaur Common Chasmosaurus Dinosaur Common Chilantaisaurus Dinosaur Rare Coelophysis Dinosaur Uncommon* Coloradisaurus Dinosaur Common* Compsognathus Dinosaur Rare* Corythosaurus Dinosaur Common* Cryolophosaurus Dinosaur Rare Cynognathus Dinosaur Rare Dacentrurus Dinosaur Common* Daspletosaurus Dinosaur Rare Datousaurus Dinosaur Common Deinocheirus Dinosaur Rare* Deinonychus Dinosaur Uncommon* Deinosuchus Dinosaur Rare* Diceratops -
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A review of the systematic position of the dinosauriform archosaur Eucoelophysis baldwini Sullivan & Lucas, 1999 from the Upper Triassic of New Mexico, USA Martín D. EZCURRA Laboratorio de Anatomia Comparada y Evolución de los Vertebrados, Museo Argentino de Ciencias Naturales “Bernardino Rivadavia”, Av. Angel Gallardo 470, Buenos Aires (1405) (Argentina) [email protected] Ezcurra M. D. 2006. — A review of the systematic position of the dinosauriform archosaur Eucoelophysis baldwini Sullivan & Lucas, 1999 from the Upper Triassic of New Mexico, USA. Geodiversitas 28 (4) : 649-684. Abstract Eucoelophysis baldwini Sullivan & Lucas, 1999 is represented by several post- cranial elements from the Petrified Forest Formation (Norian), New Mexico, USA. Eucoelophysis Sullivan & Lucas, 1999 was widely considered as a coelo- physoid dinosaur by several authors, but the hindlimb anatomy of this genus clearly indicates that it belongs to neither of these groups. The following fea- tures exclude Eucoelophysis from Neotheropoda: absence of oblique ligament groove on caudal surface of femoral head, femoral medial epicondyle small and smoothly rounded, absence of caudal cleft between medial part of the proximal end of the tibia and fibular condyles, cnemial crest low, and fibular crest absent. Moreover, Eucoelophysis lacks dinosaurian synapomorphic characters, but has a plesiomorphic slightly inturned femoral head that prevents its assignment to Dinosauria. Interestingly, the morphology of the femur of Eucoelophysis is extremely similar to that of the basal dinosauriform Silesaurus opolensis Dzik, Key words Dinosauriformes, 2003 from the Late Triassic of Poland. In order to determine the phylogenetic Coelophysoidea, position of Eucoelophysis, a cladistic analysis was carried out, which depicts Eu- Eucoelophysis, coelophysis as a non-dinosaurian dinosauriform. -
A New Raptorial Dinosaur with Exceptionally Long Feathering Provides Insights Into Dromaeosaurid flight Performance
ARTICLE Received 11 Apr 2014 | Accepted 11 Jun 2014 | Published 15 Jul 2014 DOI: 10.1038/ncomms5382 A new raptorial dinosaur with exceptionally long feathering provides insights into dromaeosaurid flight performance Gang Han1, Luis M. Chiappe2, Shu-An Ji1,3, Michael Habib4, Alan H. Turner5, Anusuya Chinsamy6, Xueling Liu1 & Lizhuo Han1 Microraptorines are a group of predatory dromaeosaurid theropod dinosaurs with aero- dynamic capacity. These close relatives of birds are essential for testing hypotheses explaining the origin and early evolution of avian flight. Here we describe a new ‘four-winged’ microraptorine, Changyuraptor yangi, from the Early Cretaceous Jehol Biota of China. With tail feathers that are nearly 30 cm long, roughly 30% the length of the skeleton, the new fossil possesses the longest known feathers for any non-avian dinosaur. Furthermore, it is the largest theropod with long, pennaceous feathers attached to the lower hind limbs (that is, ‘hindwings’). The lengthy feathered tail of the new fossil provides insight into the flight performance of microraptorines and how they may have maintained aerial competency at larger body sizes. We demonstrate how the low-aspect-ratio tail of the new fossil would have acted as a pitch control structure reducing descent speed and thus playing a key role in landing. 1 Paleontological Center, Bohai University, 19 Keji Road, New Shongshan District, Jinzhou, Liaoning Province 121013, China. 2 Dinosaur Institute, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, California 90007, USA. 3 Institute of Geology, Chinese Academy of Geological Sciences, 26 Baiwanzhuang Road, Beijing 100037, China. 4 University of Southern California, Health Sciences Campus, BMT 403, Mail Code 9112, Los Angeles, California 90089, USA. -
Brains and Intelligence
BRAINS AND INTELLIGENCE The EQ or Encephalization Quotient is a simple way of measuring an animal's intelligence. EQ is the ratio of the brain weight of the animal to the brain weight of a "typical" animal of the same body weight. Assuming that smarter animals have larger brains to body ratios than less intelligent ones, this helps determine the relative intelligence of extinct animals. In general, warm-blooded animals (like mammals) have a higher EQ than cold-blooded ones (like reptiles and fish). Birds and mammals have brains that are about 10 times bigger than those of bony fish, amphibians, and reptiles of the same body size. The Least Intelligent Dinosaurs: The primitive dinosaurs belonging to the group sauropodomorpha (which included Massospondylus, Riojasaurus, and others) were among the least intelligent of the dinosaurs, with an EQ of about 0.05 (Hopson, 1980). Smartest Dinosaurs: The Troodontids (like Troödon) were probably the smartest dinosaurs, followed by the dromaeosaurid dinosaurs (the "raptors," which included Dromeosaurus, Velociraptor, Deinonychus, and others) had the highest EQ among the dinosaurs, about 5.8 (Hopson, 1980). The Encephalization Quotient was developed by the psychologist Harry J. Jerison in the 1970's. J. A. Hopson (a paleontologist from the University of Chicago) did further development of the EQ concept using brain casts of many dinosaurs. Hopson found that theropods (especially Troodontids) had higher EQ's than plant-eating dinosaurs. The lowest EQ's belonged to sauropods, ankylosaurs, and stegosaurids. A SECOND BRAIN? It used to be thought that the large sauropods (like Brachiosaurus and Apatosaurus) and the ornithischian Stegosaurus had a second brain. -
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. -
Evaluating the Ecology of Spinosaurus: Shoreline Generalist Or Aquatic Pursuit Specialist?
Palaeontologia Electronica palaeo-electronica.org Evaluating the ecology of Spinosaurus: Shoreline generalist or aquatic pursuit specialist? David W.E. Hone and Thomas R. Holtz, Jr. ABSTRACT The giant theropod Spinosaurus was an unusual animal and highly derived in many ways, and interpretations of its ecology remain controversial. Recent papers have added considerable knowledge of the anatomy of the genus with the discovery of a new and much more complete specimen, but this has also brought new and dramatic interpretations of its ecology as a highly specialised semi-aquatic animal that actively pursued aquatic prey. Here we assess the arguments about the functional morphology of this animal and the available data on its ecology and possible habits in the light of these new finds. We conclude that based on the available data, the degree of adapta- tions for aquatic life are questionable, other interpretations for the tail fin and other fea- tures are supported (e.g., socio-sexual signalling), and the pursuit predation hypothesis for Spinosaurus as a “highly specialized aquatic predator” is not supported. In contrast, a ‘wading’ model for an animal that predominantly fished from shorelines or within shallow waters is not contradicted by any line of evidence and is well supported. Spinosaurus almost certainly fed primarily from the water and may have swum, but there is no evidence that it was a specialised aquatic pursuit predator. David W.E. Hone. Queen Mary University of London, Mile End Road, London, E1 4NS, UK. [email protected] Thomas R. Holtz, Jr. Department of Geology, University of Maryland, College Park, Maryland 20742 USA and Department of Paleobiology, National Museum of Natural History, Washington, DC 20560 USA. -
Xjiiie'icanj/Useum
XJiiie'ican1ox4tatreJ/useum PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK 24, N.Y. NUMBER 2I8I JUNE 4, I964 Relationships of the Saurischian Dinosaurs BY EDWIN H. COLBERT1 INTRODUCTION The word "Dinosauria" was coined by Sir Richard Owen in 1842 as a designation for various genera and species of extinct reptiles, the fossil bones of which were then being discovered and described in Europe. For many years this term persisted as the name for one order of reptiles and thus became well intrenched within the literature of paleontology. In- deed, since this name was associated with fossil remains that are frequently of large dimensions and spectacular shape and therefore of considerable interest to the general public, it in time became Anglicized, to take its proper place as a common noun in the English language. Almost every- body in the world is today more or less familiar with dinosaurs. As long ago as 1888, H. G. Seeley recognized the fact that the dino- saurs are not contained within a single reptilian order, but rather are quite clearly members of two distinct orders, each of which can be de- fined on the basis of many osteological characters. The structure of the pelvis is particularly useful in the separation of the two dinosaurian orders, and consequently Seeley named these two major taxonomic categories the Saurischia and the Ornithischia. This astute observation by Seeley was not readily accepted, so that for many years following the publication of his original paper proposing the basic dichotomy of the dinosaurs the 1 Chairman and Curator, Department ofVertebrate Paleontology, the American Museum of Natural History. -
Dinosaurs British Isles
DINOSAURS of the BRITISH ISLES Dean R. Lomax & Nobumichi Tamura Foreword by Dr Paul M. Barrett (Natural History Museum, London) Skeletal reconstructions by Scott Hartman, Jaime A. Headden & Gregory S. Paul Life and scene reconstructions by Nobumichi Tamura & James McKay CONTENTS Foreword by Dr Paul M. Barrett.............................................................................10 Foreword by the authors........................................................................................11 Acknowledgements................................................................................................12 Museum and institutional abbreviations...............................................................13 Introduction: An age-old interest..........................................................................16 What is a dinosaur?................................................................................................18 The question of birds and the ‘extinction’ of the dinosaurs..................................25 The age of dinosaurs..............................................................................................30 Taxonomy: The naming of species.......................................................................34 Dinosaur classification...........................................................................................37 Saurischian dinosaurs............................................................................................39 Theropoda............................................................................................................39 -
Upper Cretaceous), Brazil
Rev. Mus. Argentino Cienc. Nat., n.s. 7(1): 31-36, 2005 Buenos Aires, ISSN 1514-5158 Maniraptoran theropod ungual from the Marília Formation (Upper Cretaceous), Brazil Fernando E. NOVAS1, Luiz Carlos BORGES RIBEIRO2,3 & Ismar de SOUZA CARVALHO4 1CONICET - Museo Argentino de Ciencias Naturales «Bernardino Rivadavia», Av. Angel Gallardo 470, Buenos Aires (1405), Argentina, E-mail: [email protected]. 2Fundação Municipal de Ensino Superior de Uberaba- FUMESU/Centro de Pesquisas Paleontológicas L. I. Price. Av. Randolfo Borges Jr., n° 1.250. Universidade, 38.066-005, Uberaba- MG, Brazil, E-mail: [email protected]. 3Universidade de Uberaba-UNIUBE/Instituto de Formação de Educadores-Departamento de Biologia, Av. Nenê Sabino, n° 1.801. Universitário, Uberaba-MG, 38.055-500, Brazil, E-mail: [email protected]. 4Universidade Federal do Rio de Janeiro, Departamento de Geologia, CCMN/IGEO. 21.949-900 Cidade Universitária-Ilha do Fundão, Rio de Janeiro-RJ, Brazil, E-mail: [email protected] Abstract: A new theropod record from the Marília Formation (Late Cretaceous, Minas Gerais, Brazil) is here described. It consists of an isolated manual ungual which exhibits derived maniraptoran features (e.g., presence of proximodorsal lip). The ungual distinguishes by a set of unique features (e.g., dorsoventrally low and proximodistally elongate profile in side view; block-like flexor tuberosity; proximal articular surface more dorsally oriented than in other theropods; cutting «keel» located distally on ventral surface) suggesting that the animal that produced it was a member of an unknown group of derived maniraptoran theropods, other than alvarezsaurids, deinonychosaurians and oviraptorosaurians already recorded in South America. -
Paleopathological Analysis of a Sub-Adult Allosaurus Fragilis (MOR
Paleopathological analysis of a sub-adult Allosaurus fragilis (MOR 693) from the Upper Jurassic Morrison Formation with multiple injuries and infections by Rebecca Rochelle Laws A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Earth Sciences Montana State University © Copyright by Rebecca Rochelle Laws (1996) Abstract: A sub-adult Allosaurus fragilis (Museum of the Rockies specimen number 693 or MOR 693; "Big Al") with nineteen abnormal skeletal elements was discovered in 1991 in the Upper Jurassic Morrison Formation in Big Horn County, Wyoming at what became known as the "Big Al" site. This site is 300 meters northeast of the Howe Quarry, excavated in 1934 by Barnum Brown. The opisthotonic position of the allosaur indicated that rigor mortis occurred before burial. Although the skeleton was found within a fluvially-deposited sandstone, the presence of mud chips in the sandstone matrix and virtual completeness of the skeleton showed that the skeleton was not transported very far, if at all. The specific goals of this study are to: 1) provide a complete description and analysis of the abnormal bones of the sub-adult, male, A. fragilis, 2) develop a better understanding of how the bones of this allosaur reacted to infection and trauma, and 3) contribute to the pathological bone database so that future comparative studies are possible, and the hypothesis that certain abnormalities characterize taxa may be evaluated. The morphology of each of the 19 abnormal bones is described and each disfigurement is classified as to its cause: 5 trauma-induced; 2 infection-induced; 1 trauma- and infection-induced; 4 trauma-induced or aberrant, specific origin unknown; 4 aberrant; and 3 aberrant, specific origin unknown. -
The Pelvic and Hind Limb Anatomy of the Stem-Sauropodomorph Saturnalia Tupiniquim (Late Triassic, Brazil)
PaleoBios 23(2):1–30, July 15, 2003 © 2003 University of California Museum of Paleontology The pelvic and hind limb anatomy of the stem-sauropodomorph Saturnalia tupiniquim (Late Triassic, Brazil) MAX CARDOSO LANGER Department of Earth Sciences, University of Bristol, Wills Memorial Building, Queens Road, BS8 1RJ Bristol, UK. Current address: Departamento de Biologia, Universidade de São Paulo (USP), Av. Bandeirantes, 3900 14040-901 Ribeirão Preto, SP, Brazil; [email protected] Three partial skeletons allow a nearly complete description of the sacrum, pelvic girdle, and hind limb of the stem- sauropodomorph Saturnalia tupiniquim, from the Late Triassic Santa Maria Formation, South Brazil. The new morphological data gathered from these specimens considerably improves our knowledge of the anatomy of basal dinosaurs, providing the basis for a reassessment of various morphological transformations that occurred in the early evolution of these reptiles. These include an increase in the number of sacral vertebrae, the development of a brevis fossa, the perforation of the acetabulum, the inturning of the femoral head, as well as various modifications in the insertion of the iliofemoral musculature and the tibio-tarsal articulation. In addition, the reconstruction of the pelvic musculature of Saturnalia, along with a study of its locomotion pattern, indicates that the hind limb of early dinosaurs did not perform only a fore-and-aft stiff rotation in the parasagittal plane, but that lateral and medial movements of the leg were also present and important. INTRODUCTION sisting of most of the presacral vertebral series, both sides Saturnalia tupiniquim was described in a preliminary of the pectoral girdle, right humerus, partial right ulna, right fashion by Langer et al. -
Dinosaur Species List E to M
Dinosaur Species List E to M E F G • Echinodon becklesii • Fabrosaurus australis • Gallimimus bullatus • Edmarka rex • Frenguellisaurus • Garudimimus brevipes • Edmontonia longiceps ischigualastensis • Gasosaurus constructus • Edmontonia rugosidens • Fulengia youngi • Gasparinisaura • Edmontosaurus annectens • Fulgurotherium australe cincosaltensis • Edmontosaurus regalis • Genusaurus sisteronis • Edmontosaurus • Genyodectes serus saskatchewanensis • Geranosaurus atavus • Einiosaurus procurvicornis • Gigantosaurus africanus • Elaphrosaurus bambergi • Giganotosaurus carolinii • Elaphrosaurus gautieri • Gigantosaurus dixeyi • Elaphrosaurus iguidiensis • Gigantosaurus megalonyx • Elmisaurus elegans • Gigantosaurus robustus • Elmisaurus rarus • Gigantoscelus • Elopteryx nopcsai molengraaffi • Elosaurus parvus • Gilmoreosaurus • Emausaurus ernsti mongoliensis • Embasaurus minax • Giraffotitan altithorax • Enigmosaurus • Gongbusaurus shiyii mongoliensis • Gongbusaurus • Eoceratops canadensis wucaiwanensis • Eoraptor lunensis • Gorgosaurus lancensis • Epachthosaurus sciuttoi • Gorgosaurus lancinator • Epanterias amplexus • Gorgosaurus libratus • Erectopus sauvagei • "Gorgosaurus" novojilovi • Erectopus superbus • Gorgosaurus sternbergi • Erlikosaurus andrewsi • Goyocephale lattimorei • Eucamerotus foxi • Gravitholus albertae • Eucercosaurus • Gresslyosaurus ingens tanyspondylus • Gresslyosaurus robustus • Eucnemesaurus fortis • Gresslyosaurus torgeri • Euhelopus zdanskyi • Gryponyx africanus • Euoplocephalus tutus • Gryponyx taylori • Euronychodon