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Cranial Anatomy, Taxonomic Implications
[Palaeontology, Vol. 55, Part 4, 2012, pp. 743–773] CRANIAL ANATOMY, TAXONOMIC IMPLICATIONS AND PALAEOPATHOLOGY OF AN UPPER JURASSIC PLIOSAUR (REPTILIA: SAUROPTERYGIA) FROM WESTBURY, WILTSHIRE, UK by JUDYTH SASSOON1, LESLIE F. NOE` 2 and MICHAEL J. BENTON1* 1School of Earth Sciences, University of Bristol, Wills Memorial Building, Queen’s Road, Bristol BS8 1RJ, UK; e-mails: [email protected], [email protected] 2Geociencias, departamento de Fisica, Universidad de los Andes, Bogota´ DC, Colombia; e-mail: [email protected] *Corresponding author. Typescript received 5 December 2010; accepted in revised form 6 April 2011 Abstract: Complete skulls of giant marine reptiles of the genera. The two Westbury Pliosaurus specimens share many Late Jurassic are rare, and so the discovery of the 1.8-m- features, including the form of the teeth, but marked differ- long skull of a pliosaur from the Kimmeridge Clay Forma- ences in the snout and parietal crest suggest sexual dimor- tion (Kimmeridgian) of Westbury, Wiltshire, UK, is an phism; the present specimen is probably female. The large important find. The specimen shows most of the cranial size of the animal, the extent of sutural fusion and the and mandibular anatomy, as well as a series of pathological pathologies suggest this is an ageing individual. An erosive conditions. It was previously referred to Pliosaurus brachy- arthrotic condition of the articular glenoids led to pro- spondylus, but it can be referred reliably only to the genus longed jaw misalignment, generating a suite of associated Pliosaurus, because species within the genus are currently in bone and dental pathologies. -
O'keefe, F. R. 2006
12 Neoteny and the Plesiomorphic Condition of the Plesiosaur Basicranium F. Robin O’Keefe Introduction Historically, the systematics of the Plesiosauria (Reptilia, Sauroptery- gia) were based largely on postcranial characters (Persson, 1963; Brown, 1981). Several factors account for this bias: plesiosaur skulls tend to be del- icate and are often crushed even when preserved, postcranial elements are relatively common and cranial elements are not, lack of knowledge about the relationships of stem-group sauropterygians, and lack of knowledge of plesiosaur cranial anatomy itself. However, recent detailed examinations of plesiosaur cranial anatomy have identified many characters of use in plesiosaur systematics (Brown, 1993; Cruickshank, 1994; Storrs & Taylor, 1996; Storrs, 1997; Carpenter, 1997; Evans, 1999; O’Keefe, 2001, 2004), and the systematics of the group have changed markedly in response (Carpenter, 1997; O’Keefe, 2001, 2004). The work of Rieppel and others has clarified the anatomy and relationships of stem-group sauropterygians (Storrs, 1991; see Rieppel, 2000, for review). This work has laid the anatomic and phylogenetic foundations for a better understanding of ple- siosaur cranial anatomy. The purpose of this paper is to describe the condition of the braincase in stratigraphically early and morphologically primitive plesiosaurs. In- formation on the braincase of plesiomorphic taxa is important because it establishes the polarity of characters occurring in more derived ple- siosaurs. This paper begins with a short review of braincase anatomy in stem-group sauropterygians. Data on braincase morphology of the ple- siomorphic plesiosaur genera Thalassiodracon and Eurycleidus are then presented and interpreted via comparison with other plesiosaurs, stem- group sauropterygians, and stem diapsids (Araeoscelis). -
Marine Reptiles
Species group report card – marine reptiles Supporting the marine bioregional plan for the North Marine Region prepared under the Environment Protection and Biodiversity Conservation Act 1999 Disclaimer © Commonwealth of Australia 2012 This work is copyright. Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the Commonwealth. Requests and enquiries concerning reproduction and rights should be addressed to Department of Sustainability, Environment, Water, Population and Communities, Public Affairs, GPO Box 787 Canberra ACT 2601 or email [email protected] Images: A gorgonian wtih polyps extended – Geoscience Australia, Hawksbill Turtle – Paradise Ink, Crested Tern fishing – R.Freeman, Hard corals – A.Heyward and M.Rees, Morning Light – I.Kiessling, Soft corals – A.Heyward and M.Rees, Snubfin Dolphin – D.Thiele, Shrimp, scampi and brittlestars – A.Heyward and M.Rees, Freshwater sawfish – R.Pillans, CSIRO Marine and Atmospheric Research, Yellowstripe Snapper – Robert Thorn and DSEWPaC ii | Supporting the marine bioregional plan for the North Marine Region | Species group report card – marine reptiles CONTENTS Species group report card – marine reptiles ..........................................................................1 1. Marine reptiles of the North Marine Region .............................................................................3 2. Vulnerabilities and pressures ................................................................................................ -
El Museo De La Plata En El Avance Del Conocimiento Geológico a Fines Del Siglo XIX
Historia de la Geología Argentina I Serie Correlación Geológica, 24: 259-270 EF.G.N MAceñolazaUSEO DE (Coordinador-Editor) LA PLATA A FINES DEL SIGLO XIX Tucumán, 2008 - ISSN 1514-4186 - ISSN on-line 1666-9479259 El Museo de La Plata en el avance del conocimiento geológico a fines del Siglo XIX Alberto C. RICCARDI1 Abstract: THE LA PLATA MUSEUM……….- The contributions of the La Plata Museum to the geological knowledge of Argentina, began after this institution was founded in 1884, as an aftermath of the exploratory trips began by F.P. Moreno in 1873. The geological studies of the La Plata Museum, organized by Moreno, covered the Andean region between Puna and Tierra del Fuego, but with their main focus in the Patagonias Andes, took relevance from 1893 onwards when they became related to geographic explorations aimed at fixing the boundary between Argentina and Chile. As a result in about ten years the geographic and geological basis of extense and almost unknown regions were established. The study of the area between the Ultima Esperanza Inlet and lago Belgrano was mainly due to R. Hauthal, who defined its general stratigraphy and published the first geological map of the cordilleran region between c. 49° 30' and 52° S. The general geological scheme north of Lago Buenos Aires, to río Negro, was established by Santiago Roth. The stratigraphic succes- sion, facies and structural changes through the argentine-chilean cordillera at the latitude of Lago Nahuel Huapi and Lago Lacar was studied by L. Wehrli, whilst at the latitude of Neuquén and Mendoza is mainly due to C. -
Schmitz, M. D. 2000. Appendix 2: Radioisotopic Ages Used In
Appendix 2 Radioisotopic ages used in GTS2020 M.D. SCHMITZ 1285 1286 Appendix 2 GTS GTS Sample Locality Lat-Long Lithostratigraphy Age 6 2s 6 2s Age Type 2020 2012 (Ma) analytical total ID ID Period Epoch Age Quaternary À not compiled Neogene À not compiled Pliocene Miocene Paleogene Oligocene Chattian Pg36 biotite-rich layer; PAC- Pieve d’Accinelli section, 43 35040.41vN, Scaglia Cinerea Fm, 42.3 m above base of 26.57 0.02 0.04 206Pb/238U B2 northeastern Apennines, Italy 12 29034.16vE section Rupelian Pg35 Pg20 biotite-rich layer; MCA- Monte Cagnero section (Chattian 43 38047.81vN, Scaglia Cinerea Fm, 145.8 m above base 31.41 0.03 0.04 206Pb/238U 145.8, equivalent to GSSP), northeastern Apennines, Italy 12 28003.83vE of section MCA/84-3 Pg34 biotite-rich layer; MCA- Monte Cagnero section (Chattian 43 38047.81vN, Scaglia Cinerea Fm, 142.8 m above base 31.72 0.02 0.04 206Pb/238U 142.8 GSSP), northeastern Apennines, Italy 12 28003.83vE of section Eocene Priabonian Pg33 Pg19 biotite-rich layer; MASS- Massignano (Oligocene GSSP), near 43.5328 N, Scaglia Cinerea Fm, 14.7 m above base of 34.50 0.04 0.05 206Pb/238U 14.7, equivalent to Ancona, northeastern Apennines, 13.6011 E section MAS/86-14.7 Italy Pg32 biotite-rich layer; MASS- Massignano (Oligocene GSSP), near 43.5328 N, Scaglia Cinerea Fm, 12.9 m above base of 34.68 0.04 0.06 206Pb/238U 12.9 Ancona, northeastern Apennines, 13.6011 E section Italy Pg31 Pg18 biotite-rich layer; MASS- Massignano (Oligocene GSSP), near 43.5328 N, Scaglia Cinerea Fm, 12.7 m above base of 34.72 0.02 0.04 206Pb/238U -
Mesozoic Marine Reptile Palaeobiogeography in Response to Drifting Plates
ÔØ ÅÒÙ×Ö ÔØ Mesozoic marine reptile palaeobiogeography in response to drifting plates N. Bardet, J. Falconnet, V. Fischer, A. Houssaye, S. Jouve, X. Pereda Suberbiola, A. P´erez-Garc´ıa, J.-C. Rage, P. Vincent PII: S1342-937X(14)00183-X DOI: doi: 10.1016/j.gr.2014.05.005 Reference: GR 1267 To appear in: Gondwana Research Received date: 19 November 2013 Revised date: 6 May 2014 Accepted date: 14 May 2014 Please cite this article as: Bardet, N., Falconnet, J., Fischer, V., Houssaye, A., Jouve, S., Pereda Suberbiola, X., P´erez-Garc´ıa, A., Rage, J.-C., Vincent, P., Mesozoic marine reptile palaeobiogeography in response to drifting plates, Gondwana Research (2014), doi: 10.1016/j.gr.2014.05.005 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. ACCEPTED MANUSCRIPT Mesozoic marine reptile palaeobiogeography in response to drifting plates To Alfred Wegener (1880-1930) Bardet N.a*, Falconnet J. a, Fischer V.b, Houssaye A.c, Jouve S.d, Pereda Suberbiola X.e, Pérez-García A.f, Rage J.-C.a and Vincent P.a,g a Sorbonne Universités CR2P, CNRS-MNHN-UPMC, Département Histoire de la Terre, Muséum National d’Histoire Naturelle, CP 38, 57 rue Cuvier, -
Contributions in BIOLOGY and GEOLOGY
MILWAUKEE PUBLIC MUSEUM Contributions In BIOLOGY and GEOLOGY Number 51 November 29, 1982 A Compendium of Fossil Marine Families J. John Sepkoski, Jr. MILWAUKEE PUBLIC MUSEUM Contributions in BIOLOGY and GEOLOGY Number 51 November 29, 1982 A COMPENDIUM OF FOSSIL MARINE FAMILIES J. JOHN SEPKOSKI, JR. Department of the Geophysical Sciences University of Chicago REVIEWERS FOR THIS PUBLICATION: Robert Gernant, University of Wisconsin-Milwaukee David M. Raup, Field Museum of Natural History Frederick R. Schram, San Diego Natural History Museum Peter M. Sheehan, Milwaukee Public Museum ISBN 0-893260-081-9 Milwaukee Public Museum Press Published by the Order of the Board of Trustees CONTENTS Abstract ---- ---------- -- - ----------------------- 2 Introduction -- --- -- ------ - - - ------- - ----------- - - - 2 Compendium ----------------------------- -- ------ 6 Protozoa ----- - ------- - - - -- -- - -------- - ------ - 6 Porifera------------- --- ---------------------- 9 Archaeocyatha -- - ------ - ------ - - -- ---------- - - - - 14 Coelenterata -- - -- --- -- - - -- - - - - -- - -- - -- - - -- -- - -- 17 Platyhelminthes - - -- - - - -- - - -- - -- - -- - -- -- --- - - - - - - 24 Rhynchocoela - ---- - - - - ---- --- ---- - - ----------- - 24 Priapulida ------ ---- - - - - -- - - -- - ------ - -- ------ 24 Nematoda - -- - --- --- -- - -- --- - -- --- ---- -- - - -- -- 24 Mollusca ------------- --- --------------- ------ 24 Sipunculida ---------- --- ------------ ---- -- --- - 46 Echiurida ------ - --- - - - - - --- --- - -- --- - -- - - --- -
How Plesiosaurs Swam: New Insights Into Their Underwater Flight Using “Ava”, a Virtual Pliosaur
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 9 October 2019 doi:10.20944/preprints201910.0094.v1 How Plesiosaurs Swam: New Insights into Their Underwater Flight Using “Ava”, a Virtual Pliosaur Max Hawthorne1,*, Mark A. S. McMenamin 2, Paul de la Salle3 1Far From The Tree Press, LLC, 4657 York Rd., #952, Buckingham, PA, 18912, United States 2Department of Geology and Geography, Mount Holyoke College, South Hadley, Massachusetts, United States 3Swindon, England *Correspondence: [email protected]; Tel.: 267-337-7545 Abstract Analysis of plesiosaur swim dynamics by means Further study attempted to justify the use of all four flippers of a digital 3D armature (wireframe “skeleton”) of a simultaneously via the use of paddle-generated vortices, pliosauromorph (“Ava”) demonstrates that: 1, plesiosaurs which require specific timing to achieve optimal additional used all four flippers for primary propulsion; 2, plesiosaurs thrust. These attempts have largely relied on anatomical utilized all four flippers simultaneously; 3, respective pairs studies of strata-compressed plesiosaur skeletons, and/or of flippers of Plesiosauridae, front and rear, traveled through preconceived notions as pertains to the paddles’ inherent distinctive, separate planes of motion, and; 4, the ability to ranges of motion [8, 10-12]. What has not been considered utilize all four paddles simultaneously allowed these largely are the opposing angles of the pectoral and pelvic girdles, predatory marine reptiles to achieve a significant increase in which strongly indicate varied-yet-complementing relations acceleration and speed, which, in turn, contributed to their between the front and rear sets of paddles, both in repose and sustained dominance during the Mesozoic. -
The Giant Pliosaurid That Wasn't—Revising the Marine Reptiles From
The giant pliosaurid that wasn’t—revising the marine reptiles from the Kimmeridgian, Upper Jurassic, of Krzyżanowice, Poland DANIEL MADZIA, TOMASZ SZCZYGIELSKI, and ANDRZEJ S. WOLNIEWICZ Madzia, D., Szczygielski, T., and Wolniewicz, A.S. 2021. The giant pliosaurid that wasn’t—revising the marine reptiles from the Kimmeridgian, Upper Jurassic, of Krzyżanowice, Poland. Acta Palaeontologica Polonica 66 (1): 99–129. Marine reptiles from the Upper Jurassic of Central Europe are rare and often fragmentary, which hinders their precise taxonomic identification and their placement in a palaeobiogeographic context. Recent fieldwork in the Kimmeridgian of Krzyżanowice, Poland, a locality known from turtle remains originally discovered in the 1960s, has reportedly provided additional fossils thought to indicate the presence of a more diverse marine reptile assemblage, including giant pliosaurids, plesiosauroids, and thalattosuchians. Based on its taxonomic composition, the marine tetrapod fauna from Krzyżanowice was argued to represent part of the “Matyja-Wierzbowski Line”—a newly proposed palaeobiogeographic belt comprising faunal components transitional between those of the Boreal and Mediterranean marine provinces. Here, we provide a de- tailed re-description of the marine reptile material from Krzyżanowice and reassess its taxonomy. The turtle remains are proposed to represent a “plesiochelyid” thalassochelydian (Craspedochelys? sp.) and the plesiosauroid vertebral centrum likely belongs to a cryptoclidid. However, qualitative assessment and quantitative analysis of the jaws originally referred to the colossal pliosaurid Pliosaurus clearly demonstrate a metriorhynchid thalattosuchian affinity. Furthermore, these me- triorhynchid jaws were likely found at a different, currently indeterminate, locality. A tooth crown previously identified as belonging to the thalattosuchian Machimosaurus is here considered to represent an indeterminate vertebrate. -
Sauropterygia I Placodontia, Pachypleurosauria, Nothosauroidea, Pistosauroidea
Teil 12A / Part 12A Sauropterygia I Placodontia, Pachypleurosauria, Nothosauroidea, Pistosauroidea by O. RlEPPEL With 80 Figures Verlag Dr. Friedrich Pfeil • Munchen 2000 ISBN 3-931516-78-4 Contents Foreword (P. WELLNHOFER) V Acknowledgements VI Institutional Acronyms VII Figure Abbreviations VIII Introduction: History of the Concept of Sauropterygia 1 Phylogenetic Relationships of Stem-Group Sauropterygia 4 Stratigraphic and Geographic Distribution of Stem-Group Sauropterygia 6 General Skeletal Anatomy of Stem-Group Sauropterygia 10 Systematic Review 16 Superorder Sauropterygia OWEN, 1860 16 Order Placodontia COPE, 1871 16 Suborder Placodontoidea COPE, 1871 16 Family Paraplacodontidae PEYER & KUHN-SCHNYDER, 1955 17 Anatomy of Paraplacodontidae 17 Genus Paraplacodus PEYER, 1931 18 Family Placodontidae COPE, 1871 19 Anatomy of Placodontidae 19 Genus Placodus AGASSIZ, 1933 21 Suborder Cyamodontoidea NOPCSA, 1923 23 Anatomy of Cyamodontoidea 23 Interrelationships of Cyamodontoidea 25 Superfamily Cyamodontida NOPCSA, 1923 25 Family Henodontidae F. v. HUENE, 1948 26 Genus Henodus F. v. HUENE, 1936 26 Family Cyamodontidae NOPCSA, 1923 27 Genus Cyamodus MEYER, 1863 27 Superfamily Placochelyida ROMER, 1956 32 Family Macroplacidae nov. fam 32 Genus Macroplacus SCHUBERT-KLEMPNAUER, 1975 32 Family Protenodontosauridae nov. fam 33 Genus Protenodontosaurus PINNA, 1990 33 Family Placochelyidae ROMER, 1956 34 Genus Placochelys JAEKEL, 1902 34 Genus Psephoderma MEYER, 1858 36 Genus Psephosaurus E. FRAAS, 1896 38 Cyamodontoidea indet 39 IX Order Eosauropterygia -
Exceptional Vertebrate Biotas from the Triassic of China, and the Expansion of Marine Ecosystems After the Permo-Triassic Mass Extinction
Earth-Science Reviews 125 (2013) 199–243 Contents lists available at ScienceDirect Earth-Science Reviews journal homepage: www.elsevier.com/locate/earscirev Exceptional vertebrate biotas from the Triassic of China, and the expansion of marine ecosystems after the Permo-Triassic mass extinction Michael J. Benton a,⁎, Qiyue Zhang b, Shixue Hu b, Zhong-Qiang Chen c, Wen Wen b, Jun Liu b, Jinyuan Huang b, Changyong Zhou b, Tao Xie b, Jinnan Tong c, Brian Choo d a School of Earth Sciences, University of Bristol, Bristol BS8 1RJ, UK b Chengdu Center of China Geological Survey, Chengdu 610081, China c State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences (Wuhan), Wuhan 430074, China d Key Laboratory of Evolutionary Systematics of Vertebrates, Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences, Beijing 100044, China article info abstract Article history: The Triassic was a time of turmoil, as life recovered from the most devastating of all mass extinctions, the Received 11 February 2013 Permo-Triassic event 252 million years ago. The Triassic marine rock succession of southwest China provides Accepted 31 May 2013 unique documentation of the recovery of marine life through a series of well dated, exceptionally preserved Available online 20 June 2013 fossil assemblages in the Daye, Guanling, Zhuganpo, and Xiaowa formations. New work shows the richness of the faunas of fishes and reptiles, and that recovery of vertebrate faunas was delayed by harsh environmental Keywords: conditions and then occurred rapidly in the Anisian. The key faunas of fishes and reptiles come from a limited Triassic Recovery area in eastern Yunnan and western Guizhou provinces, and these may be dated relative to shared strati- Reptile graphic units, and their palaeoenvironments reconstructed. -
Sea Monsters: a Prehiistoriic Adventure Summatiive Evalluatiion Report
Sea Monsters: A Prehiistoriic Adventure Summatiive Evalluatiion Report Prepared for Natiionall Geographiic Ciinema Ventures By Valleriie Kniight-Wiilllliiams, Ed.D. Diivan Wiilllliiams Jr., J.D. Chriistiina Meyers, M.A. Ora Sraboyants, B.A. Wiith assiistance from: Stanlley Chan Eveen Chan Eva Wiilllliiams Daviid Tower Mason Bonner-Santos Knight-Williams Research Communications November 2008 This material is based on work supported by the National Science Foundation under Cooperative Agreement No. 0514981. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of the National Science Foundation. Knight-Williams Table of Contents CREDITS............................................................................................................................................................................................ 1 INTRODUCTION................................................................................................................................................................................ 2 THEATER CONTEXT ........................................................................................................................................................................ 4 METHOD............................................................................................................................................................................................ 8 SAMPLE INFORMATION...............................................................................................................................................................