Insight on the Anatomy, Systematic Relationships, and Age of the Early Cretaceous Ankylopollexian Dinosaur Dakotadon Lakotaensis Clint A
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MEET the DINOSAURS! WHAT’S in a NAME? a LOT If You Are a Dinosaur!
MEET THE DINOSAURS! WHAT’S IN A NAME? A LOT if you are a dinosaur! I will call you Dyoplosaurus! Most dinosaurs get their names from the ancient Greek and Latin languages. And I will call you Mojoceratops! And sometimes they are named after a defining feature on their body. Their names are made up of word parts that describe the dinosaur. The name must be sent to a special group of people called the International Commission on Zoological Nomenclature to be approved! Did You The word DINOSAUR comes from the Greek word meaning terrible lizard and was first said by Know? Sir Richard Owen in 1841. © 2013 Omaha’s Henry Doorly Zoo & Aquarium® | 3 SEE IF YOU CAN FIND OUT THE MEANING OF SOME OF OUR DINOSAUR’S NAMES. Dinosaur names are not just tough to pronounce, they often have meaning. Dinosaur Name MEANING of Dinosaur Name Carnotaurus (KAR-no-TORE-us) Means “flesh-eating bull” Spinosaurus (SPY-nuh-SORE-us) Dyoplosaurus (die-o-pluh-SOR-us) Amargasaurus (ah-MAR-guh-SORE-us) Omeisaurus (Oh-MY-ee-SORE-us) Pachycephalosaurus (pak-ee-SEF-uh-low-SORE-us) Tuojiangosaurus (toh-HWANG-uh-SORE-us) Yangchuanosaurus (Yang-chew-ON-uh-SORE-us) Quetzalcoatlus (KWET-zal-coe-AT-lus) Ouranosaurus (ooh-RAN-uh-SORE-us) Parasaurolophus (PAIR-uh-so-ROL-uh-PHUS) Kosmoceratops (KOZ-mo-SARA-tops) Mojoceratops (moe-joe-SEH-rah-tops) Triceratops (try-SER-uh-TOPS) Tyrannosaurus rex (tuh-RAN-uh-SORE-us) Find the answers by visiting the Resource Library at Carnotaurus A: www.OmahaZoo.com/Education. Search word: Dinosaurs 4 | © 2013 Omaha’s Henry Doorly Zoo & Aquarium® DINO DEFENSE All animals in the wild have to protect themselves. -
At Carowinds
at Carowinds EDUCATOR’S GUIDE CLASSROOM LESSON PLANS & FIELD TRIP ACTIVITIES Table of Contents at Carowinds Introduction The Field Trip ................................... 2 The Educator’s Guide ....................... 3 Field Trip Activity .................................. 4 Lesson Plans Lesson 1: Form and Function ........... 6 Lesson 2: Dinosaur Detectives ....... 10 Lesson 3: Mesozoic Math .............. 14 Lesson 4: Fossil Stories.................. 22 Games & Puzzles Crossword Puzzles ......................... 29 Logic Puzzles ................................. 32 Word Searches ............................... 37 Answer Keys ...................................... 39 Additional Resources © 2012 Dinosaurs Unearthed Recommended Reading ................. 44 All rights reserved. Except for educational fair use, no portion of this guide may be reproduced, stored in a retrieval system, or transmitted in any form or by any Dinosaur Data ................................ 45 means—electronic, mechanical, photocopy, recording, or any other without Discovering Dinosaurs .................... 52 explicit prior permission from Dinosaurs Unearthed. Multiple copies may only be made by or for the teacher for class use. Glossary .............................................. 54 Content co-created by TurnKey Education, Inc. and Dinosaurs Unearthed, 2012 Standards www.turnkeyeducation.net www.dinosaursunearthed.com Curriculum Standards .................... 59 Introduction The Field Trip From the time of the first exhibition unveiled in 1854 at the Crystal -
Camptosaurus Dispar Legs; Although, the Smaller Juveniles Might Have Been Able to Do So
Camptosaurus was too front heavy to walk on hind Camptosaurus dispar legs; although, the smaller juveniles might have been able to do so. e skull of Camptosaurus is about 15 inches long. It has no teeth at the front of the beak and broad crushing teeth in the cheeks. ese teeth are made stronger by ridges on the outer surface. Chewing causes these teeth to have a at, grinding surface. Unlike Allosaurus, these teeth cannot slice through esh, but they can pulverize vegetation. Our skeleton of Camptosaurus went on display Scienti c Name: Camptosaurus dispar at the museum around 1965 and was the Muse- Pronounced: KAMP-toe-SOR-us um’s second dinosaur skeleton. Originally, it was Name Meaning: Flexible lizard mounted in the kangaroo pose on its hind legs and Time Period: 147 Million Years Ago (MYA) Late using its tail as a prop. It was remounted into a new Jurassic four-legged pose in 2013 . e skeleton is 17¾ feet Length:16-23 feet (5-7 m) long long and 5 feet tall at the hips. It is a plaster of Paris Height: 3-4 feet (1 m) high at the hips cast of bones collected from the Cleveland Lloyd Weight: 2,200 pounds (1000 kg). Dinosaur Quarry, about 30 miles south of Price. Diet: Herbivore (plant eater) e pelvis is rather broad for its length and the Places Found: Camptosaurus was a distant relative of Iguanodon, upper bone, called the ilium, bows outwards. Discoverer: Marsh (1885) the dinosaur with the thumb-spike. In fact, the thumb (digit I) of Camptosaurus had little move- e hand of Camptosaurus has ve digits, but only ment and the claw was almost like a spike . -
A Phylogenetic Analysis of the Basal Ornithischia (Reptilia, Dinosauria)
A PHYLOGENETIC ANALYSIS OF THE BASAL ORNITHISCHIA (REPTILIA, DINOSAURIA) Marc Richard Spencer A Thesis Submitted to the Graduate College of Bowling Green State University in partial fulfillment of the requirements of the degree of MASTER OF SCIENCE December 2007 Committee: Margaret M. Yacobucci, Advisor Don C. Steinker Daniel M. Pavuk © 2007 Marc Richard Spencer All Rights Reserved iii ABSTRACT Margaret M. Yacobucci, Advisor The placement of Lesothosaurus diagnosticus and the Heterodontosauridae within the Ornithischia has been problematic. Historically, Lesothosaurus has been regarded as a basal ornithischian dinosaur, the sister taxon to the Genasauria. Recent phylogenetic analyses, however, have placed Lesothosaurus as a more derived ornithischian within the Genasauria. The Fabrosauridae, of which Lesothosaurus was considered a member, has never been phylogenetically corroborated and has been considered a paraphyletic assemblage. Prior to recent phylogenetic analyses, the problematic Heterodontosauridae was placed within the Ornithopoda as the sister taxon to the Euornithopoda. The heterodontosaurids have also been considered as the basal member of the Cerapoda (Ornithopoda + Marginocephalia), the sister taxon to the Marginocephalia, and as the sister taxon to the Genasauria. To reevaluate the placement of these taxa, along with other basal ornithischians and more derived subclades, a phylogenetic analysis of 19 taxonomic units, including two outgroup taxa, was performed. Analysis of 97 characters and their associated character states culled, modified, and/or rescored from published literature based on published descriptions, produced four most parsimonious trees. Consistency and retention indices were calculated and a bootstrap analysis was performed to determine the relative support for the resultant phylogeny. The Ornithischia was recovered with Pisanosaurus as its basalmost member. -
Rule Booklet
Dig for fossils, build skeletons, and attract the most visitors to your museum! TM SCAN FOR VIDEO RULES AND MORE! FOSSILCANYON.COM Dinosaurs of North America edimentary rock formations of western North America are famous for the fossilized remains of dinosaurs The rules are simple enough for young players, but and other animals from the Triassic, Jurassic, and serious players can benefit Cretaceous periods of the Mesozoic Era. Your objective from keeping track of the cards that is to dig up fossils, build complete skeletons, and display have appeared, reasoning about them in your museum to attract as many visitors as possible. probabilities and expected returns, and choosing between aggressive Watch your museum’s popularity grow using jigsaw-puzzle and conservative plays. scoring that turns the competition into a race! GAME CONTENTS TM 200,000300,000 160,000 VISITORS VISITORS PER YEAR 140,000 VISITORS PER YEAR 180,000 VISITORS PER YEAR 400,000 VISITORS PER YEAR Dig for fossils, build skeletons, and 340,000 VISITORS PER YEAR RD COLOR ELETONS CA GENUS PERIODDIET SK FOSSIL VISITORSPARTS 360,000 VISITORS PER YEAR PER YEAR attract the most visitors to your museum! VISITORS PER YEAR PER YEAR Tyrannosaurus K C 1 4 500,000 Brachiosaurus J H 1 3 400,000 ON YOUR TURN: TM SCAN FOR VIDEO Triceratops K H 1 3 380,000 RULES AND MORE! Allosaurus J C 2 Dig3 a first360,000 card. If it is a fossil, keep it hidden. FOSSILCANYON.COM Ankylosaurus K H 2 If it3 is an340,000 action card, perform the action. -
A Revised Taxonomy of the Iguanodont Dinosaur Genera and Species
ARTICLE IN PRESS + MODEL Cretaceous Research xx (2007) 1e25 www.elsevier.com/locate/CretRes A revised taxonomy of the iguanodont dinosaur genera and species Gregory S. Paul 3109 North Calvert Station, Side Apartment, Baltimore, MD 21218-3807, USA Received 20 April 2006; accepted in revised form 27 April 2007 Abstract Criteria for designating dinosaur genera are inconsistent; some very similar species are highly split at the generic level, other anatomically disparate species are united at the same rank. Since the mid-1800s the classic genus Iguanodon has become a taxonomic grab-bag containing species spanning most of the Early Cretaceous of the northern hemisphere. Recently the genus was radically redesignated when the type was shifted from nondiagnostic English Valanginian teeth to a complete skull and skeleton of the heavily built, semi-quadrupedal I. bernissartensis from much younger Belgian sediments, even though the latter is very different in form from the gracile skeletal remains described by Mantell. Currently, iguanodont remains from Europe are usually assigned to either robust I. bernissartensis or gracile I. atherfieldensis, regardless of lo- cation or stage. A stratigraphic analysis is combined with a character census that shows the European iguanodonts are markedly more morpho- logically divergent than other dinosaur genera, and some appear phylogenetically more derived than others. Two new genera and a new species have been or are named for the gracile iguanodonts of the Wealden Supergroup; strongly bipedal Mantellisaurus atherfieldensis Paul (2006. Turning the old into the new: a separate genus for the gracile iguanodont from the Wealden of England. In: Carpenter, K. (Ed.), Horns and Beaks: Ceratopsian and Ornithopod Dinosaurs. -
Titanosauriform Teeth from the Cretaceous of Japan
“main” — 2011/2/10 — 15:59 — page 247 — #1 Anais da Academia Brasileira de Ciências (2011) 83(1): 247-265 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 www.scielo.br/aabc Titanosauriform teeth from the Cretaceous of Japan HARUO SAEGUSA1 and YUKIMITSU TOMIDA2 1Museum of Nature and Human Activities, Hyogo, Yayoigaoka 6, Sanda, 669-1546, Japan 2National Museum of Nature and Science, 3-23-1 Hyakunin-cho, Shinjuku-ku, Tokyo 169-0073, Japan Manuscript received on October 25, 2010; accepted for publication on January 7, 2011 ABSTRACT Sauropod teeth from six localities in Japan were reexamined. Basal titanosauriforms were present in Japan during the Early Cretaceous before Aptian, and there is the possibility that the Brachiosauridae may have been included. Basal titanosauriforms with peg-like teeth were present during the “mid” Cretaceous, while the Titanosauria with peg-like teeth was present during the middle of Late Cretaceous. Recent excavations of Cretaceous sauropods in Asia showed that multiple lineages of sauropods lived throughout the Cretaceous in Asia. Japanese fossil records of sauropods are conformable with this hypothesis. Key words: Sauropod, Titanosauriforms, tooth, Cretaceous, Japan. INTRODUCTION humerus from the Upper Cretaceous Miyako Group at Moshi, Iwaizumi Town, Iwate Pref. (Hasegawa et al. Although more than twenty four dinosaur fossil local- 1991), all other localities provided fossil teeth (Tomida ities have been known in Japan (Azuma and Tomida et al. 2001, Tomida and Tsumura 2006, Saegusa et al. 1998, Kobayashi et al. 2006, Saegusa et al. 2008, Ohara 2008, Azuma and Shibata 2010). -
Abstract Book.Pdf
Welcome! Welcome to the VI Symposium on Dinosaur Eggs and Babies, the return of this periodic gathering to the Iberian Peninsula, when it hatched eighteen years ago. From the slopes of the Pyrenees, we have followed the first steps of dinosaurs through France, Argentina, the United States and China. Today, we come back and see the coast where the first theropod embryos were discovered twenty years ago. Since the end of the last century, Paleoology, much like other branches of palaeontology, has evolved thanks to the advance of new methodologies and analytical tools, becoming a progressively more interdisciplinary area of knowledge. Dinosaur babies and embryos, rare findings back when these meetings started, seem to be everywhere now that we learn to look for them under the light of the microscope. New astonishing specimens allow us to understand how Mesozoic dinosaurs mate and reproduce. Oology, our parent discipline in the modern world, has made great advances in understanding the form and function of the egg, and its applications on poultry industry are countless. More than thirty contributions evidence that our field remains small but alive and healthy. We hope that you find in this Symposium an opportunity to share knowledge and open new lines of collaboration. And do not forget to enjoy your stay in Portugal. The host committee CONTENTS How to get to the FCT 6 Acknowledgements 10 PROGRAM 11 ABSTRACTS 14 THE FIRST ORNITHOMIMID EMBRYO IN A SHELL WITH A SINGLE STRUCTURAL LAYER: A CHALLENGE TO ORTHODOXY 15 Araújo R., Lamb J., Atkinson P., Martins R. M. S., Polcyn M.J., Fernandez V. -
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 -
From the Early Cretaceous of Morella, Spain
RESEARCH ARTICLE A New Sail-Backed Styracosternan (Dinosauria: Ornithopoda) from the Early Cretaceous of Morella, Spain José Miguel Gasulla1☯, Fernando Escaso2☯*, Iván Narváez2, Francisco Ortega2, José Luis Sanz1 1 Unidad de Paleontología, Universidad Autónoma de Madrid, Cantoblanco, Madrid, Spain, 2 Grupo de Biología Evolutiva, Universidad Nacional de Educación a Distancia, Madrid, Spain ☯ These authors contributed equally to this work. * [email protected] Abstract A new styracosternan ornithopod genus and species is here described based on a partial postcranial skeleton and an associated dentary tooth of a single specimen from the Arcillas de Morella Formation (Early Cretaceous, late Barremian) at the Morella locality, (Castellón, Spain). Morelladon beltrani gen. et sp. nov. is diagnosed by eight autapomorphic features. The set of autapomorphies includes: very elongated and vertical neural spines of the dorsal vertebrae, midline keel on ventral surface of the second to fourth sacral vertebrae restricted OPEN ACCESS to the anterior half of the centrum, a posterodorsally inclined medial ridge on the postace- Citation: Gasulla JM, Escaso F, Narváez I, Ortega F, tabular process of the ilium that meets its dorsal margin and distal end of the straight ischial Sanz JL (2015) A New Sail-Backed Styracosternan shaft laterally expanded, among others. Phylogenetic analyses reveal that the new Iberian (Dinosauria: Ornithopoda) from the Early Cretaceous of Morella, Spain. PLoS ONE 10(12): e0144167. form is more closely related to its synchronic and sympatric contemporary European taxa doi:10.1371/journal.pone.0144167 Iguanodon bernissartensis and Mantellisaurus atherfieldensis, known from Western Editor: Leon Claessens, College of the Holy Cross, Europe, than to other Early Cretaceous Iberian styracosternans (Delapparentia turolensis UNITED STATES and Proa valdearinnoensis). -
Phylogeny and Biogeography of Iguanodontian Dinosaurs, with Implications from Ontogeny and an Examination of the Function of the Fused Carpal-Digit I Complex
Phylogeny and Biogeography of Iguanodontian Dinosaurs, with Implications from Ontogeny and an Examination of the Function of the Fused Carpal-Digit I Complex By Karen E. Poole B.A. in Geology, May 2004, University of Pennsylvania M.A. in Earth and Planetary Sciences, August 2008, Washington University in St. Louis A Dissertation submitted to The Faculty of The Columbian College of Arts and Sciences of The George Washington University in partial fulfillment of the requirements for the degree of Doctor of Philosophy August 31, 2015 Dissertation Directed by Catherine Forster Professor of Biology The Columbian College of Arts and Sciences of The George Washington University certifies that Karen Poole has passed the Final Examination for the degree of Doctor of Philosophy as of August 10th, 2015. This is the final and approved form of the dissertation. Phylogeny and Biogeography of Iguanodontian Dinosaurs, with Implications from Ontogeny and an Examination of the Function of the Fused Carpal-Digit I Complex Karen E. Poole Dissertation Research Committee: Catherine A. Forster, Professor of Biology, Dissertation Director James M. Clark, Ronald Weintraub Professor of Biology, Committee Member R. Alexander Pyron, Robert F. Griggs Assistant Professor of Biology, Committee Member ii © Copyright 2015 by Karen Poole All rights reserved iii Dedication To Joseph Theis, for his unending support, and for always reminding me what matters most in life. To my parents, who have always encouraged me to pursue my dreams, even those they didn’t understand. iv Acknowledgements First, a heartfelt thank you is due to my advisor, Cathy Forster, for giving me free reign in this dissertation, but always providing valuable commentary on any piece of writing I sent her, no matter how messy. -
Inferring Body Mass in Extinct Terrestrial Vertebrates and the Evolution of Body Size in a Model-Clade of Dinosaurs (Ornithopoda)
Inferring Body Mass in Extinct Terrestrial Vertebrates and the Evolution of Body Size in a Model-Clade of Dinosaurs (Ornithopoda) by Nicolás Ernesto José Campione Ruben A thesis submitted in conformity with the requirements for the degree of Doctor of Philosophy Ecology and Evolutionary Biology University of Toronto © Copyright by Nicolás Ernesto José Campione Ruben 2013 Inferring body mass in extinct terrestrial vertebrates and the evolution of body size in a model-clade of dinosaurs (Ornithopoda) Nicolás E. J. Campione Ruben Doctor of Philosophy Ecology and Evolutionary Biology University of Toronto 2013 Abstract Organismal body size correlates with almost all aspects of ecology and physiology. As a result, the ability to infer body size in the fossil record offers an opportunity to interpret extinct species within a biological, rather than simply a systematic, context. Various methods have been proposed by which to estimate body mass (the standard measure of body size) that center on two main approaches: volumetric reconstructions and extant scaling. The latter are particularly contentious when applied to extinct terrestrial vertebrates, particularly stem-based taxa for which living relatives are difficult to constrain, such as non-avian dinosaurs and non-therapsid synapsids, resulting in the use of volumetric models that are highly influenced by researcher bias. However, criticisms of scaling models have not been tested within a comprehensive extant dataset. Based on limb measurements of 200 mammals and 47 reptiles, linear models were generated between limb measurements (length and circumference) and body mass to test the hypotheses that phylogenetic history, limb posture, and gait drive the relationship between stylopodial circumference and body mass as critics suggest.