By Leonie Bennett

Total Page:16

File Type:pdf, Size:1020Kb

By Leonie Bennett by Leonie Bennett 1417_COVER_DinoBabies.indd 1 7/3/07 10:24:57 AM [Intentionally Left Blank] Dinosaur Babies by Leonie Bennett Consultant: Luis M. Chiappe, Ph.D. Director of the Dinosaur Institute Natural History Museum of Los Angeles County 1417_Dino Babies_FINAL.indd 1 6/20/07 3:37:35 PM Credits Cover, Title Page: Pulsar EStudio; 4, 6TR, 6BR, 8–9, 16: Simon Mendez; 5, 7, 12–13, 13TR, 17, 18, 19, 22, 24: Philip Hood; 6TL, 6BL, 23: Shutterstock; 10, 11, 20–21: Luis Rey; 13TL: Corbis; 14–15: Pulsar EStudio. Every effort has been made by ticktock Entertainment Ltd. to trace copyright holders. We apologize in advance for any omissions. We would be pleased to insert the appropriate acknowledgments in any subsequent edition of this publication. Library of Congress Cataloging-in-Publication Data Bennett, Leonie. Dinosaur babies / by Leonie Bennett. p. cm. — (I love reading. Dino world!) Includes bibliographical references and index. ISBN-13: 978-1-59716-544-0 (library binding) ISBN-10: 1-59716-544-1 (library binding) 1. Dinosaurs—Infancy—Juvenile literature. 2. Dinosaurs—Juvenile literature. I. Title. QE861.5.B4452 2008 567.9—dc22 2007017655 Copyright © 2007 ticktock Entertainment Ltd. 2 Orchard Business Centre, North Farm Road, Tunbridge Wells, Kent, TN2 3XF, UK Published in the United States of America by Bearport Publishing Company, Inc. United States text copyright © 2008 Bearport Publishing Company, Inc. No part of this publication may be reproduced, in whole or in part, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, recording or otherwise without prior written permission from the publisher. For more information, write to Bearport Publishing Company, Inc., 101 Fifth Avenue, Suite 6R, New York, New York 10003. Printed in the United States of America. 10 9 8 7 6 5 4 3 2 1 1417_Dino Babies_FINAL.indd 2 6/21/07 1:12:10 PM Contents Dinosaur eggs . 4 How big were dinosaur eggs?. 6 Laying eggs . 8 Protecting their eggs . 10 How big were dinosaur babies? . 12 Caring for babies . 14 What did dinosaur babies eat? . 16 A special dinosaur mother. 18 Sea babies . 20 Glossary . 22 Index . 24 Read More . 24 Learn More Online . 24 1417_Dino Babies_FINAL.indd 3 6/28/07 4:04:05 PM Dinosaur eggs Dinosaurs laid eggs. Then the eggs hatched. Baby dinosaurs came out of them. Troodon eggs were oval. Troodon eggs Troodon 4 (TROH-oh-don) 1417_Dino Babies_FINAL.indd 4 6/20/07 3:37:42 PM Therizinosaurus eggs were round. Therizinosaurus (ther-uh-zeen-oh-SOR-uhss) Therizinosaurus egg 5 1417_Dino Babies_FINAL.indd 5 6/20/07 3:37:47 PM How big were dinosaur eggs? Some eggs were bigger than a soccer ball. Some eggs were smaller than a golf ball. 6 1417_Dino Babies_FINAL.indd 6 6/20/07 3:37:50 PM The biggest dinosaur egg found so far came from Hypselosaurus. It was about 1 foot (30 cm) long. Hypselosaurus (hip-sel-oh-SOR-uhss) 7 1417_Dino Babies_FINAL.indd 7 6/20/07 3:37:57 PM Index Apatosaurus 12 Oviraptor 10 Hypselosaurus 7 Plesiosaurus 9 Ichthyosaurus 21 Therizinosaurus 5 Maiasaura 18–19 Triceratops 15 Mussaurus 13 Troodon 4 Read More Lessem, Don. Baby Randall, Lee. A Day Dinosaurs (When in the Life of a Baby Dinosaurs Lived). New Dinosaur. Mahwah, NJ: York: Grosset & Dunlap Troll Communications (2001). (1996). Learn More Online To learn more about the world of dinosaurs, visit www.bearportpublishing.com/ILoveReading 24 1417_Dino Babies_FINAL.indd 24 6/21/07 10:36:29 AM [Intentionally Left Blank] Dinosaur Babies Amazing Dinosaur Facts Dinosaur Babies They may have started off small, but some baby dinosaurs Dinosaur Fossils grew into the biggest animals Dinosaur Hunting in the world. Discover how these babies were born and Fighting Dinosaurs how they found food to survive. Flying Giants Really Big Dinosaurs and Other Giants Swimming Giants 1417_COVER_DinoBabies.indd 1 7/3/07 10:24:57 AM.
Recommended publications
  • A New Troodontid Theropod, Talos Sampsoni Gen. Et Sp. Nov., from the Upper Cretaceous Western Interior Basin of North America
    A New Troodontid Theropod, Talos sampsoni gen. et sp. nov., from the Upper Cretaceous Western Interior Basin of North America Lindsay E. Zanno1,2*, David J. Varricchio3, Patrick M. O’Connor4,5, Alan L. Titus6, Michael J. Knell3 1 Field Museum of Natural History, Chicago, Illinois, United States of America, 2 Biological Sciences Department, University of Wisconsin-Parkside, Kenosha, Wisconsin, United States of America, 3 Department of Earth Sciences, Montana State University, Bozeman, Montana, United States of America, 4 Department of Biomedical Sciences, Ohio University College of Osteopathic Medicine, Athens, Ohio, United States of America, 5 Ohio Center for Ecology and Evolutionary Studies, Ohio University, Athens, Ohio, United States of America, 6 Grand Staircase-Escalante National Monument, Bureau of Land Management, Kanab, Utah, United States of America Abstract Background: Troodontids are a predominantly small-bodied group of feathered theropod dinosaurs notable for their close evolutionary relationship with Avialae. Despite a diverse Asian representation with remarkable growth in recent years, the North American record of the clade remains poor, with only one controversial species—Troodon formosus—presently known from substantial skeletal remains. Methodology/Principal Findings: Here we report a gracile new troodontid theropod—Talos sampsoni gen. et sp. nov.— from the Upper Cretaceous Kaiparowits Formation, Utah, USA, representing one of the most complete troodontid skeletons described from North America to date. Histological assessment of the holotype specimen indicates that the adult body size of Talos was notably smaller than that of the contemporary genus Troodon. Phylogenetic analysis recovers Talos as a member of a derived, latest Cretaceous subclade, minimally containing Troodon, Saurornithoides, and Zanabazar.
    [Show full text]
  • Theropod Teeth from the Upper Maastrichtian Hell Creek Formation “Sue” Quarry: New Morphotypes and Faunal Comparisons
    Theropod teeth from the upper Maastrichtian Hell Creek Formation “Sue” Quarry: New morphotypes and faunal comparisons TERRY A. GATES, LINDSAY E. ZANNO, and PETER J. MAKOVICKY Gates, T.A., Zanno, L.E., and Makovicky, P.J. 2015. Theropod teeth from the upper Maastrichtian Hell Creek Formation “Sue” Quarry: New morphotypes and faunal comparisons. Acta Palaeontologica Polonica 60 (1): 131–139. Isolated teeth from vertebrate microfossil localities often provide unique information on the biodiversity of ancient ecosystems that might otherwise remain unrecognized. Microfossil sampling is a particularly valuable tool for doc- umenting taxa that are poorly represented in macrofossil surveys due to small body size, fragile skeletal structure, or relatively low ecosystem abundance. Because biodiversity patterns in the late Maastrichtian of North American are the primary data for a broad array of studies regarding non-avian dinosaur extinction in the terminal Cretaceous, intensive sampling on multiple scales is critical to understanding the nature of this event. We address theropod biodiversity in the Maastrichtian by examining teeth collected from the Hell Creek Formation locality that yielded FMNH PR 2081 (the Tyrannosaurus rex specimen “Sue”). Eight morphotypes (three previously undocumented) are identified in the sample, representing Tyrannosauridae, Dromaeosauridae, Troodontidae, and Avialae. Noticeably absent are teeth attributed to the morphotypes Richardoestesia and Paronychodon. Morphometric comparison to dromaeosaurid teeth from multiple Hell Creek and Lance formations microsites reveals two unique dromaeosaurid morphotypes bearing finer distal denticles than present on teeth of similar size, and also differences in crown shape in at least one of these. These findings suggest more dromaeosaurid taxa, and a higher Maastrichtian biodiversity, than previously appreciated.
    [Show full text]
  • A. K. Rozhdestvensky HISTORY of the DINOSAUR FAUNA of ASIA
    A. K. Rozhdestvensky HISTORY OF THE DINOSAUR FAUNA OF ASIA AND OTHER CONTINENTS AND QUESTIONS CONCERNING PALEOGEOGRAPHY* The distribution and evolution of dinosaur faunas during the period of their existence, from the Late Triassic to the end of the Cretaceous, shows a close connection with the paleogeography of the Mesozoic. However these questions were hard to examine on a global scale until recently, because only the dinosaurs of North America were well known, where during the last century were found their richest deposits and where the best paleontologists were studying them — J. Leidy, E. Cope, O. Marsh, R. Lull, H. Osborn, C. Gilmore, B. Brown, and later many others. On the remaining continents, including Europe, where the study of dinosaurs started earlier than it did in America, the information was rather incomplete due to the fragmentary condition of the finds and rare, episodic studies. The Asian continent remained unexplored the longest, preventing any intercontinental comparisons. Systematic exploration and large excavations of dinosaur locations in Asia, which began in the last fifty years (Osborn, 1930; Efremov, 1954; Rozhdestvenskiy, 1957a, 1961, 1969, 1971; Rozhdestvenskiy & Chzhou, 1960; Kielan-Jaworowska & Dovchin, 1968; Kurochkin, Kalandadze, & Reshetov, 1970; Barsbold, Voronin, & Zhegallo, 1971) showed that this continent has abundant dinosaur remains, particularly in its central part (Fig. 1). Their study makes it possible to establish a faunal connection between Asia and other continents, correlate the stratigraphy of continental deposits of the Mesozoic, because dinosaurs are reliable leading forms, as well as to make corrections in the existing paleogeographic structure. The latter, in their turn, promote a better understanding of the possible paths of distribution of the individual groups of dinosaurs, the reasons for their appearance, their development, and disappearance.
    [Show full text]
  • Titanosaur, Titano- Sauridae
    Cambridge University Press 978-0-521-77930-2 - Dinosaur Impressions: Postcards from a Paleontologist Philippe Taquet Index More information INDEX FOR ECONOMY, informal and formal names of taxa (titanosaur, Titano­ sauridae) as well as eponymous genera (Titanosaurus) are often listed under a single joint entry. Illustration pages are followed by an "f." Bachelet. Abbe. 177 Afrovenator, 220 Agades, 2, 3,4, 5, 15,22,25, 53, 63, 66 Bacot. J., l30-1 Air. 3. 4. 53. 66 Baharija. 19lf., 192 Aix-en-Provence. 169, 198-200 Bahia. 81-2. 83-4. 92-4 Alexander. R. M .. 59 Bakker, R. T.. 118-21, 202, 203 Algui Ulan Tsav, 133, 136. l37 6. 7 barkhanes. Allport. S .• 82. 93 Barsbold. R .. 124. 128. l30. l37. 145 Alvarez. 1.. 208. 216 Baryonychidae. 193 Baryonyx. Alvarez. W., 208 Battuta, I., 4 American Museum of Natural History. Bayeux. 187 125-8. 138. 144, 151. 223 Bayn Dzak, 127. 128. 134. 138 Andrews. R. c.. 125-8. l34. l38. 223 Beaumont. E. de. 215. 217 Ankylosauria, 33. 35, 132. 200, 225 Beni Mellat, 95, 96. 100 Annam, Annamite Range, 147. 149, 160 Bernissart. 30. 33. 38, 41 66 Bertrand. M .. 96-7 anou, Aodelbi.66 Bessonat. G .. 62 Aoulef. 75. 76 Bidou. H .. 117 44-5, 113, 115 biogeography. 89. 220 Apatosaurus. birds, 194-8. 207 Araripesaurus, 92 90-1. 92. 93. 94 relationship to dinosaurs, 195-8. 205. Araripesuchus. 194-7. 224 223 Archaeopteryx. Archibald. J. D., 207 Bleustein-Blanchot. M .. 71 Archosauria. 34. 201-2. 220 Bonaparte. J. F.. 220. 222 Argentina, 220-1 Boulenger.
    [Show full text]
  • 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.
    [Show full text]
  • Perinate and Eggs of a Giant Caenagnathid Dinosaur from the Late Cretaceous of Central China
    ARTICLE Received 29 Jul 2016 | Accepted 15 Feb 2017 | Published 9 May 2017 DOI: 10.1038/ncomms14952 OPEN Perinate and eggs of a giant caenagnathid dinosaur from the Late Cretaceous of central China Hanyong Pu1, Darla K. Zelenitsky2, Junchang Lu¨3, Philip J. Currie4, Kenneth Carpenter5,LiXu1, Eva B. Koppelhus4, Songhai Jia1, Le Xiao1, Huali Chuang1, Tianran Li1, Martin Kundra´t6 & Caizhi Shen3 The abundance of dinosaur eggs in Upper Cretaceous strata of Henan Province, China led to the collection and export of countless such fossils. One of these specimens, recently repatriated to China, is a partial clutch of large dinosaur eggs (Macroelongatoolithus) with a closely associated small theropod skeleton. Here we identify the specimen as an embryo and eggs of a new, large caenagnathid oviraptorosaur, Beibeilong sinensis. This specimen is the first known association between skeletal remains and eggs of caenagnathids. Caenagnathids and oviraptorids share similarities in their eggs and clutches, although the eggs of Beibeilong are significantly larger than those of oviraptorids and indicate an adult body size comparable to a gigantic caenagnathid. An abundance of Macroelongatoolithus eggs reported from Asia and North America contrasts with the dearth of giant caenagnathid skeletal remains. Regardless, the large caenagnathid-Macroelongatoolithus association revealed here suggests these dinosaurs were relatively common during the early Late Cretaceous. 1 Henan Geological Museum, Zhengzhou 450016, China. 2 Department of Geoscience, University of Calgary, Calgary, Alberta, Canada T2N 1N4. 3 Institute of Geology, Chinese Academy of Geological Sciences, Beijing 100037, China. 4 Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E9. 5 Prehistoric Museum, Utah State University, 155 East Main Street, Price, Utah 84501, USA.
    [Show full text]
  • 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).
    [Show full text]
  • Norntates PUBLISHED by the AMERICAN MUSEUM of NATURAL HISTORY CENTRAL PARK WEST at 79TH STREET, NEW YORK, NY 10024 Number 3265, 36 Pp., 15 Figures May 4, 1999
    AMERICANt MUSEUM Norntates PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK, NY 10024 Number 3265, 36 pp., 15 figures May 4, 1999 An Oviraptorid Skeleton from the Late Cretaceous of Ukhaa Tolgod, Mongolia, Preserved in an Avianlike Brooding Position Over an Oviraptorid Nest JAMES M. CLARK,I MARK A. NORELL,2 AND LUIS M. CHIAPPE3 ABSTRACT The articulated postcranial skeleton of an ovi- presence of a single, ossified ventral segment in raptorid dinosaur (Theropoda, Coelurosauria) each rib as well as ossified uncinate processes from the Late Cretaceous Djadokhta Formation associated with the thoracic ribs. Remnants of of Ukhaa Tolgod, Mongolia, is preserved over- keratinous sheaths are preserved with four of the lying a nest. The eggs are similar in size, shape, manal claws, and the bony and keratinous claws and ornamentation to another egg from this lo- were as strongly curved as the manal claws of cality in which an oviraptorid embryo is pre- Archaeopteryx and the pedal claws of modern served, suggesting that the nest is of the same climbing birds. The skeleton is positioned over species as the adult skeleton overlying it and was the center of the nest, with its limbs arranged parented by the adult. The lack of a skull pre- symmetrically on either side and its arms spread cludes specific identification, but in several fea- out around the nest perimeter. This is one of four tures the specimen is more similar to Oviraptor known oviraptorid skeletons preserved on nests than to other oviraptorids. The ventral part of the of this type of egg, comprising 23.5% of the 17 thorax is exceptionally well preserved and pro- oviraptorid skeletons collected from the Dja- vides evidence for other avian features that were dokhta Formation before 1996.
    [Show full text]
  • 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
    [Show full text]
  • Lyons SCIENCE 2021 the Influence of Juvenile Dinosaurs SUPPL.Pdf
    science.sciencemag.org/content/371/6532/941/suppl/DC1 Supplementary Materials for The influence of juvenile dinosaurs on community structure and diversity Katlin Schroeder*, S. Kathleen Lyons, Felisa A. Smith *Corresponding author. Email: [email protected] Published 26 February 2021, Science 371, 941 (2021) DOI: 10.1126/science.abd9220 This PDF file includes: Materials and Methods Supplementary Text Figs. S1 and S2 Tables S1 to S7 References Other Supplementary Material for this manuscript includes the following: (available at science.sciencemag.org/content/371/6532/941/suppl/DC1) MDAR Reproducibility Checklist (PDF) Materials and Methods Data Dinosaur assemblages were identified by downloading all vertebrate occurrences known to species or genus level between 200Ma and 65MA from the Paleobiology Database (PaleoDB 30 https://paleobiodb.org/#/ download 6 August, 2018). Using associated depositional environment and taxonomic information, the vertebrate database was limited to only terrestrial organisms, excluding amphibians, pseudosuchians, champsosaurs and ichnotaxa. Taxa present in formations were confirmed against the most recent available literature, as of November, 2020. Synonymous taxa or otherwise duplicated taxa were removed. Taxa that could not be identified to genus level 35 were included as “Taxon X”. GPS locality data for all formations between 200MA and 65MA was downloaded from PaleoDB to create a minimally convex polygon for each possible formation. Any attempt to recreate local assemblages must include all potentially interacting species, while excluding those that would have been separated by either space or time. We argue it is 40 acceptable to substitute formation for home range in the case of non-avian dinosaurs, as range increases with body size.
    [Show full text]
  • Hierarchical Clustering Analysis Suppcdr.Cdr
    Distance Hierarchical joiningclustering 3.0 2.5 2.0 1.5 1.0 0.5 Sinosauropteryx Caudipteryx Eoraptor Compsognathus Compsognathus Compsognathus Compsognathus Megaraptora basal Coelurosauria Noasauridae Neotheropoda non-averostran T non-tyrannosaurid Dromaeosauridae basalmost Theropoda Oviraptorosauria Compsognathidae Therizinosauria T A yrannosauroidea Compsognathus roodontidae ves Compsognathus Compsognathus Compsognathus Compsognathus Compsognathus Compsognathus Compsognathus Compsognathus Compsognathus Compsognathus Compsognathus Compsognathus Compsognathus Richardoestesia Scipionyx Buitreraptor Compsognathus Troodon Compsognathus Compsognathus Compsognathus Juravenator Sinosauropteryx Juravenator Juravenator Sinosauropteryx Incisivosaurus Coelophysis Scipionyx Richardoestesia Compsognathus Compsognathus Compsognathus Richardoestesia Richardoestesia Richardoestesia Richardoestesia Compsognathus Richardoestesia Juravenator Richardoestesia Richardoestesia Richardoestesia Richardoestesia Buitreraptor Saurornitholestes Ichthyornis Saurornitholestes Ichthyornis Richardoestesia Richardoestesia Richardoestesia Richardoestesia Richardoestesia Juravenator Scipionyx Buitreraptor Coelophysis Richardoestesia Coelophysis Richardoestesia Richardoestesia Richardoestesia Richardoestesia Coelophysis Richardoestesia Bambiraptor Richardoestesia Richardoestesia Velociraptor Juravenator Saurornitholestes Saurornitholestes Buitreraptor Coelophysis Coelophysis Ornitholestes Richardoestesia Richardoestesia Juravenator Saurornitholestes Velociraptor Saurornitholestes
    [Show full text]
  • Cranial Osteology of Beipiaosaurus Inexpectus
    第57卷 第2期 古 脊 椎 动 物 学 报 pp. 117–132 figs. 1–3 2019年4月 VERTEBRATA PALASIATICA DOI: 10.19615/j.cnki.1000-3118.190115 Cranial osteology of Beipiaosaurus inexpectus (Theropoda: Therizinosauria) LIAO Chun-Chi1,2,3 XU Xing1,2* (1 Key Laboratory of Vertebrate Evolution and Human Origins of Chinese Academy of Sciences, Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences Beijing 100044 * Corresponding author: [email protected]) (2 CAS Center for Excellence in Life and Paleoenvironment Beijing 100044) (3 University of Chinese Academy of Sciences Beijing 100049) Abstract Beipiaosaurus inexpectus, a key taxon for understanding the early evolution of therizinosaurians, has not been fully described since it was briefly reported on by Xu, Tang and Wang in 1999. Here we present a detailed description of the cranial anatomy of the holotype of this theropod dinosaur. B. inexpectus is unique in some of its cranial features such as the postorbital process of the frontal is large and its abrupt transition from the orbital rim, a long and sharp anterior process of the parietal, the elongate ventral ramus of the squamosal process of parietal, and external mandibular fenestra deep dorsoventrally and extremely posteriorly located. A number of plesiomorphic cranial features (such as relatively large dentary and less downturned degree of dentary symphysis) suggest that B. inexpectus is an early-branching Therizinosaurian, as proposed by previous studies. New information derived from our study is not only important for our understanding of the cranial anatomy of B. inexpectus but also significant to the study of the evolution of Therizinosauria.
    [Show full text]