Dinosaur Journey Exhibits Guide a Teacher-Friendly Map and Explanation to the Exhibits at Dinosaur Journey
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Two New Stegosaur Specimens from the Upper Jurassic Morrison Formation of Montana, USA
Editors' choice Two new stegosaur specimens from the Upper Jurassic Morrison Formation of Montana, USA D. CARY WOODRUFF, DAVID TREXLER, and SUSANNAH C.R. MAIDMENT Woodruff, D.C., Trexler, D., and Maidment, S.C.R. 2019. Two new stegosaur specimens from the Upper Jurassic Morrison Formation of Montana, USA. Acta Palaeontologica Polonica 64 (3): 461–480. Two partial skeletons from Montana represent the northernmost occurrences of Stegosauria within North America. One of these specimens represents the northernmost dinosaur fossil ever recovered from the Morrison Formation. Consisting of fragmentary cranial and postcranial remains, these specimens are contributing to our knowledge of the record and distribution of dinosaurs within the Morrison Formation from Montana. While the stegosaurs of the Morrison Formation consist of Alcovasaurus, Hesperosaurus, and Stegosaurus, the only positively identified stegosaur from Montana thus far is Hesperosaurus. Unfortunately, neither of these new specimens exhibit diagnostic autapomorphies. Nonetheless, these specimens are important data points due to their geographic significance, and some aspects of their morphologies are striking. In one specimen, the teeth express a high degree of wear usually unobserved within this clade—potentially illuminating the progression of the chewing motion in derived stegosaurs. Other morphologies, though not histologically examined in this analysis, have the potential to be important indicators for maturational inferences. In suite with other specimens from the northern extent of the formation, these specimens contribute to the ongoing discussion that body size may be latitudinally significant for stegosaurs—an intriguing geographical hypothesis which further emphasizes that size is not an undeviating proxy for maturity in dinosaurs. Key words: Dinosauria, Thyreophora, Stegosauria, Jurassic, Morrison Formation, USA, Montana. -
A New Microvertebrate Assemblage from the Mussentuchit
A new microvertebrate assemblage from the Mussentuchit Member, Cedar Mountain Formation: insights into the paleobiodiversity and paleobiogeography of early Late Cretaceous ecosystems in western North America Haviv M. Avrahami1,2,3, Terry A. Gates1, Andrew B. Heckert3, Peter J. Makovicky4 and Lindsay E. Zanno1,2 1 Department of Biological Sciences, North Carolina State University, Raleigh, NC, USA 2 North Carolina Museum of Natural Sciences, Raleigh, NC, USA 3 Department of Geological and Environmental Sciences, Appalachian State University, Boone, NC, USA 4 Field Museum of Natural History, Chicago, IL, USA ABSTRACT The vertebrate fauna of the Late Cretaceous Mussentuchit Member of the Cedar Mountain Formation has been studied for nearly three decades, yet the fossil-rich unit continues to produce new information about life in western North America approximately 97 million years ago. Here we report on the composition of the Cliffs of Insanity (COI) microvertebrate locality, a newly sampled site containing perhaps one of the densest concentrations of microvertebrate fossils yet discovered in the Mussentuchit Member. The COI locality preserves osteichthyan, lissamphibian, testudinatan, mesoeucrocodylian, dinosaurian, metatherian, and trace fossil remains and is among the most taxonomically rich microvertebrate localities in the Mussentuchit Submitted 30 May 2018 fi fi Accepted 8 October 2018 Member. To better re ne taxonomic identi cations of isolated theropod dinosaur Published 16 November 2018 teeth, we used quantitative analyses of taxonomically comprehensive databases of Corresponding authors theropod tooth measurements, adding new data on theropod tooth morphodiversity in Haviv M. Avrahami, this poorly understood interval. We further provide the first descriptions of [email protected] tyrannosauroid premaxillary teeth and document the earliest North American record of Lindsay E. -
Stegosaurus Scelidosaurus Huayangosaurus Cheeks: No
Huayangosaurus Scelidosaurus Stegosaurus Cheeks: No reptile has ever had a ‘buccinator’ muscle Answer: highly flexible tongue Brains 0.001% of stegosaur body weight Compared to 1.8% in humans (1000x larger per unit body weight!) Brains Brains Locomotion Graviportal Locomotion Elephantine hind feet (weight-bearing) Shin bones fused with astragalus/ calcaneum Femur: Long compared to humerus Columnar Facultative Tripodality? Stocky forelimbs- could be used for turning/posturing (Bakker) Dermal Armour? Pattern of plates and spines is species-specific Plates paired or staggered (Stegosaurus) Plates were probably not for defense... not tough enough Rotation? Surface markings => symmetrical. Rotation unlikely Potential uses: Thermoregulation? Warm up (ectotherms), Cool down (endotherms) Signaling? positioned for maximal lateral visibility Sexual Selection Mate Recognition Grooves for blood vessels Sexual dimorphism Differences between males and females of the same species **New finding** published in 2015 Stegosaurus Morrison formation, Colorado Dinosaur Sex Figuring out how Stegosaurus even could have mated is a prickly subject. Females were just as well-armored as males, and it is unlikely that males mounted the females from the back. A different technique was necessary. Perhaps they angled so that they faced belly to belly, some have guessed, or maybe, as suggested by Timothy Isles in a recent paper, males faced away from standing females and backed up (a rather tricky maneuver!). The simplest technique yet proposed is that the female lay down on her side and the male approached standing up, thereby avoiding all those plates and spikes. However the Stegosaurus pair accomplished the feat, though, it was most likely brief—only as long as was needed for the exchange of genetic material. -
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 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. -
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. -
The Systematic Position of the Enigmatic Thyreophoran Dinosaur Paranthodon Africanus, and the Use of Basal Exemplifiers in Phyl
1 The systematic position of the enigmatic thyreophoran dinosaur Paranthodon africanus, 2 and the use of basal exemplifiers in phylogenetic analysis 3 4 Thomas J. Raven1,2 ,3 and Susannah C. R. Maidment2 ,3 5 61Department of Earth Science & Engineering, Imperial College London, UK 72School of Environment & Technology, University of Brighton, UK 8 3Department of Earth Sciences, Natural History Museum, London, UK 9 10Corresponding author: Thomas J. Raven 11 12Email address: [email protected] 13 14 15 16 17 18 19 20 21ABSTRACT 22 23The first African dinosaur to be discovered, Paranthodon africanus was found in 1845 in the 24Lower Cretaceous of South Africa. Taxonomically assigned to numerous groups since discovery, 25in 1981 it was described as a stegosaur, a group of armoured ornithischian dinosaurs 26characterised by bizarre plates and spines extending from the neck to the tail. This assignment 27that has been subsequently accepted. The type material consists of a premaxilla, maxilla, a nasal, 28and a vertebra, and contains no synapomorphies of Stegosauria. Several features of the maxilla 29and dentition are reminiscent of Ankylosauria, the sister-taxon to Stegosauria, and the premaxilla 30appears superficially similar to that of some ornithopods. The vertebral material has never been 31described, and since the last description of the specimen, there have been numerous discoveries 32of thyreophoran material potentially pertinent to establishing the taxonomic assignment of the 33specimen. An investigation of the taxonomic and systematic position of Paranthodon is therefore 34warranted. This study provides a detailed re-description, including the first description of the 35vertebra. Numerous phylogenetic analyses demonstrate that the systematic position of 36Paranthodon is highly labile and subject to change depending on which exemplifier for the clade 37Stegosauria is used. -
Ankylosaurid Dinosaur Tail Clubs Evolved Through Stepwise Acquisition of Key Features
1 Title: Ankylosaurid dinosaur tail clubs evolved through stepwise acquisition of key features. 2 3 Victoria M. Arbour1,2,3 and Philip J. Currie3 4 1Paleontology and Geology Research Laboratory, North Carolina Museum of Natural Sciences, Raleigh, 5 North Carolina 27601, USA; 2Department of Biological Sciences, North Carolina State University, Raleigh, 6 North Carolina, 27607, USA; 3Department of Biological Sciences, University of Alberta, Edmonton, 7 Alberta, T6G 2E9, Canada; [email protected] 8 Corresponding author: V. Arbour 9 10 Running title: ANKYLOSAURID TAIL CLUB STEPWISE EVOLUTION 11 12 13 14 15 16 17 18 19 20 21 22 23 24 1 25 ABSTRACT 26 Ankylosaurid ankylosaurs were quadrupedal, herbivorous dinosaurs with abundant dermal 27 ossifications. They are best known for their distinctive tail club composed of stiff, interlocking vertebrae 28 (the handle) and large, bulbous osteoderms (the knob), which may have been used as a weapon. 29 However, tail clubs appear relatively late in the evolution of ankylosaurids, and seemed to have been 30 present only in a derived clade of ankylosaurids during the last 20 million years of the Mesozoic Era. 31 New evidence from mid Cretaceous fossils from China suggests that the evolution of the tail club 32 occurred at least 40 million years earlier, and in a stepwise manner, with early ankylosaurids evolving 33 handle-like vertebrae before the distal osteoderms enlarged and coossified to form a knob. 34 35 Keywords: Dinosauria, Ankylosauria, Ankylosauridae, Cretaceous 36 37 38 39 40 41 42 43 44 45 46 47 48 2 49 INTRODUCTION 50 Tail weaponry, in the form of spikes or clubs, is an uncommon adaptation among tetrapods. -
The Fighting Pair
THE FIGHTING PAIR ALLOSAURUS VS STEGOSAURUS — Allosaurus “jimmadsoni” and Hesperosaurus (Stegosaurus) mjosi Upper Jurassic Period, Kimmeridgian Stage, 155 million years old Morrison Formation Dana Quarry, Ten Sleep, Washakie County, Wyoming, USA. THE ALLOSAURUS The Official State Fossil of Utah, the Allosaurus was a large theropod carnosaur of the “bird-hipped” Saurischia order that flourished primarily in North America during the Upper Jurassic Period, 155-145 million years In the spring of 2007, at the newly-investigated Dana Quarry in the Morrison Formation of Wyoming, the team from ago. Long recognized in popular culture, it bears the distinction of being Dinosauria International LLC made an exciting discovery: the beautifully preserved femur of the giant carnivorous one of the first dinosaurs to be depicted on the silver screen, the apex Allosaur. As they kept digging, their excitement grew greater; next came toe bones, leg bones, ribs, vertebrae and predator of the 1912 novel and 1925 cinema adaptation of Conan Doyle’s finally a skull: complete, undistorted and, remarkably, with full dentition. It was an incredible find; one of the most The Lost World. classic dinosaurs, virtually complete, articulated and in beautiful condition. But that was not all. When the team got The Allosaurus possessed a large head on a short neck, a broad rib-cage the field jackets back to the preparation lab, they discovered another leg bone beneath the Allosaurus skull… There creating a barrel chest, small three-fingered forelimbs, large powerful hind limbs with hoof-like feet, and a long heavy tail to act as a counter-balance. was another dinosaur in the 150 million year-old rock. -
Oil and Gas Plays Ute Moutnain Ute Reservation, Colorado and New Mexico
Ute Mountain Ute Indian Reservation Cortez R18W Karle Key Xu R17W T General Setting Mine Xu Xcu 36 Can y on N Xcu McElmo WIND RIVER 32 INDIAN MABEL The Ute Mountain Ute Reservation is located in the northwest RESERVATION MOUNTAIN FT HALL IND RES Little Moude Mine Xcu T N ern portion of New Mexico and the southwestern corner of Colorado UTE PEAK 35 N R16W (Fig. UM-1). The reservation consists of 553,008 acres in Montezu BLACK 666 T W Y O M I N G MOUNTAIN 35 R20W SLEEPING UTE MOUNTAIN N ma and La Plata Counties, Colorado, and San Juan County, New R19W Coche T Mexico. All of these lands belong to the tribe but are held in trust by NORTHWESTERN 34 SHOSHONI HERMANO the U.S. Government. Individually owned lands, or allotments, are IND RES Desert Canyon PEAK N MESA VERDE R14W NATIONAL GREAT SALT LAKE W Marble SENTINEL located at Allen Canyon and White Mesa, San Juan County, Utah, Wash Towaoc PARK PEAK T and cover 8,499 acres. Tribal lands held in trust within this area cov Towaoc River M E S A 33 1/2 N er 3,597 acres. An additional forty acres are defined as U.S. Govern THE MOUND R15W SKULL VALLEY ment lands in San Juan County, Utah, and are utilized for school pur TEXAS PACIFIC 6-INCH OIL PIPELINE IND RES UNITAH AND OURAY INDIAN RESERVATION Navajo poses. W Ramona GOSHUTE 789 The Allen Canyon allotments are located twelve miles west of IND RES T UTAH 33 Blanding, Utah, and adjacent to the Manti-La Sal National Forest. -
A Fossil Locality Predictive Model for the Early Cretaceous Cedar Mountain Formation, Utah, Usa
A FOSSIL LOCALITY PREDICTIVE MODEL FOR THE EARLY CRETACEOUS CEDAR MOUNTAIN FORMATION, UTAH, USA A THESIS PRESENTED TO THE DEPARTMENT OF HUMANITIES AND SOCIAL SCIENCE IN CANDIDACY FOR THE DEGREE OF MASTER OF SCIENCE By DANIEL BURK NORTHWEST MISSOURI STATE UNIVERSITY MARYVILLE, MISSOURI OCTOBER, 2014 FOSSIL LOCALITY PREDICTIVE MODEL A Fossil Locality Predictive Model for the Early Cretaceous Cedar Mountain Formation, Utah, USA Daniel Burk Northwest Missouri State University THESIS APPROVED Thesis Advisor, Dr. Yi-Hwa Wu Date Dr. Ming-Chih Hung Date Dr. John P. Pope Date Dean of Graduate School Date A Fossil Locality Predictive Model for the Early Cretaceous Cedar Mountain Formation, Utah, USA Abstract Hard work and chance are nearly always among the deciding factors in finding new, important, and productive paleontological localities. Fossil locality predictive models have the potential to reduce unproductive field time and maximize hard work thus increasing the chances researchers have to find important localities. This study uses remotely sensed data to design and test a fossil locality predictive model for the Early Cretaceous Cedar Mountain Formation. Landsat 8 OLI/TIRS data from known localities were summarized, reclassified and used in a weighted suitability analysis to categorize fossil locality potential of the study area. Field work was conducted to test model functionality. Field observations were used to refine the weighted suitability analysis. Landsat 8 OLI/TIRS data alone offers a less accurate prescription of fossil locality potential. Additional physical and environmental factors play a role in determining the chance of finding fossils. Slope degree and aspect data from known localities were summarized and analyzed to further refine the model. -
A Jurassic Basal Eusauropod Clade from Iberia Finds Refuge In
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by UCL Discovery Descendants of the Jurassic turiasaurs from Iberia found refuge in the Early Cretaceous of western USA Rafael Royo-Torres, Paul Upchurch, James I. Kirkland, Donald D. DeBlieux, John R. Foster, Alberto Cobos, Luis Alcalá Supplementary Information: I. Abbreviations section II. Geological setting of the Doelling’s Bowl bonebed III. Phylogenetic analyses and list of synapomorphies IV. Holotype of Mierasaurus V. Measurements VI. References I. Abbreviations section BYU (Museum of Paleontology of Brigham Young University, Provo, Utah USA). DBBB Doelling’s Bowl bonebed; DBGI Doelling’s Bowl site; J-K Jurassic- Cretaceous transition; Ma million years ago; My million years; MPT most parsimonious trees; RD name for every dinosaur site from Riodeva in Teruel (Spain); TL Tree length; UMNH the Natural History Museum of Utah (USA); UGS Utah Geological Survey (USA). Anatomical abbreviations: bt basal tubera; bo basioccipital; bpt basipterygoid process; ca crista antotica; ct crista tuberalis; f frontal; fme fenestra metotic; fv fenestra vestivuli (=fenestra ovalis); osc otosphenoidal crest (= crista prootica); p parietal; pa parapophysis; prf prefontal; stf supratemporal fossa; so supraoccipital; eo exoccipital- opisthotic; bo basioccipital; popr paraoccipital process; cranial nerves: I olfactory nerve; II optic nerve; III oculomotor nerve; IV trochlear nerve; V trigeminal nerve (ophthalmic, maxillary, mandibular); VI abductor or abducens nerve; VII facialis nerve; VIII vestibulocochlear nerve. Abbreviations for laminae vertebral: acpl anterior centroparapophyseal lamina; ant. spdl anterior spinodiapophyseal lamina; cprl 1 centroprezygapophyseal lamina; cpol centropostzygapophyseal lamina; pcdl posterior centrodiapophyseal lamina; post. spdl posterior spinodiapophyseal lamina; ppdl paradiapophyseal lamina; prdl prezygodiapophyseal lamina; spol spinopostzygapophyseal lamina.