Sea Monsters: a Prehistoric Adventure
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Asteroid Impact, Not Volcanism, Caused the End-Cretaceous Dinosaur Extinction
Asteroid impact, not volcanism, caused the end-Cretaceous dinosaur extinction Alfio Alessandro Chiarenzaa,b,1,2, Alexander Farnsworthc,1, Philip D. Mannionb, Daniel J. Luntc, Paul J. Valdesc, Joanna V. Morgana, and Peter A. Allisona aDepartment of Earth Science and Engineering, Imperial College London, South Kensington, SW7 2AZ London, United Kingdom; bDepartment of Earth Sciences, University College London, WC1E 6BT London, United Kingdom; and cSchool of Geographical Sciences, University of Bristol, BS8 1TH Bristol, United Kingdom Edited by Nils Chr. Stenseth, University of Oslo, Oslo, Norway, and approved May 21, 2020 (received for review April 1, 2020) The Cretaceous/Paleogene mass extinction, 66 Ma, included the (17). However, the timing and size of each eruptive event are demise of non-avian dinosaurs. Intense debate has focused on the highly contentious in relation to the mass extinction event (8–10). relative roles of Deccan volcanism and the Chicxulub asteroid im- An asteroid, ∼10 km in diameter, impacted at Chicxulub, in pact as kill mechanisms for this event. Here, we combine fossil- the present-day Gulf of Mexico, 66 Ma (4, 18, 19), leaving a crater occurrence data with paleoclimate and habitat suitability models ∼180 to 200 km in diameter (Fig. 1A). This impactor struck car- to evaluate dinosaur habitability in the wake of various asteroid bonate and sulfate-rich sediments, leading to the ejection and impact and Deccan volcanism scenarios. Asteroid impact models global dispersal of large quantities of dust, ash, sulfur, and other generate a prolonged cold winter that suppresses potential global aerosols into the atmosphere (4, 18–20). These atmospheric dinosaur habitats. -
The Endoskeletal Origin of the Turtle Carapace
ARTICLE Received 7 Dec 2012 | Accepted 3 Jun 2013 | Published 9 Jul 2013 DOI: 10.1038/ncomms3107 OPEN The endoskeletal origin of the turtle carapace Tatsuya Hirasawa1, Hiroshi Nagashima2 & Shigeru Kuratani1 The turtle body plan, with its solid shell, deviates radically from those of other tetrapods. The dorsal part of the turtle shell, or the carapace, consists mainly of costal and neural bony plates, which are continuous with the underlying thoracic ribs and vertebrae, respectively. Because of their superficial position, the evolutionary origins of these costo-neural elements have long remained elusive. Here we show, through comparative morphological and embryological analyses, that the major part of the carapace is derived purely from endos- keletal ribs. We examine turtle embryos and find that the costal and neural plates develop not within the dermis, but within deeper connective tissue where the rib and intercostal muscle anlagen develop. We also examine the fossils of an outgroup of turtles to confirm that the structure equivalent to the turtle carapace developed independently of the true osteoderm. Our results highlight the hitherto unravelled evolutionary course of the turtle shell. 1 Laboratory for Evolutionary Morphology, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan. 2 Division of Gross Anatomy and Morphogenesis, Department of Regenerative and Transplant Medicine, Niigata University, Niigata 951-8510, Japan. Correspondence and requests for materials should be addressed to T.H. (email: [email protected]). NATURE COMMUNICATIONS | 4:2107 | DOI: 10.1038/ncomms3107 | www.nature.com/naturecommunications 1 & 2013 Macmillan Publishers Limited. All rights reserved. ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms3107 wo types of skeletal systems are recognized in vertebrates, exoskeletal components into the costal and neural plates (Fig. -
The Geologic Time Scale Is the Eon
Exploring Geologic Time Poster Illustrated Teacher's Guide #35-1145 Paper #35-1146 Laminated Background Geologic Time Scale Basics The history of the Earth covers a vast expanse of time, so scientists divide it into smaller sections that are associ- ated with particular events that have occurred in the past.The approximate time range of each time span is shown on the poster.The largest time span of the geologic time scale is the eon. It is an indefinitely long period of time that contains at least two eras. Geologic time is divided into two eons.The more ancient eon is called the Precambrian, and the more recent is the Phanerozoic. Each eon is subdivided into smaller spans called eras.The Precambrian eon is divided from most ancient into the Hadean era, Archean era, and Proterozoic era. See Figure 1. Precambrian Eon Proterozoic Era 2500 - 550 million years ago Archaean Era 3800 - 2500 million years ago Hadean Era 4600 - 3800 million years ago Figure 1. Eras of the Precambrian Eon Single-celled and simple multicelled organisms first developed during the Precambrian eon. There are many fos- sils from this time because the sea-dwelling creatures were trapped in sediments and preserved. The Phanerozoic eon is subdivided into three eras – the Paleozoic era, Mesozoic era, and Cenozoic era. An era is often divided into several smaller time spans called periods. For example, the Paleozoic era is divided into the Cambrian, Ordovician, Silurian, Devonian, Carboniferous,and Permian periods. Paleozoic Era Permian Period 300 - 250 million years ago Carboniferous Period 350 - 300 million years ago Devonian Period 400 - 350 million years ago Silurian Period 450 - 400 million years ago Ordovician Period 500 - 450 million years ago Cambrian Period 550 - 500 million years ago Figure 2. -
Cretaceous - Tertiary Mass Extinction Meteoritic Versus Volcanic Causes
GENERAL I ARTICLE Cretaceous - Tertiary Mass Extinction Meteoritic Versus Volcanic Causes P V Sukumaran The bolide impact theory for mass extinctions at the Cretaceous-tertiary (K-T) boundary was a revolutionary concept. This theory was contested by short duration global volcanism as a possible alternative cause for the K-T extinction. Though there is a converging evidence for an extra-terrestrial impact coinciding with the P V Sukumaran took his terminal Cretaceous, the causative link between the M Tech degree in impact and the K-T mass extinction is debatable. Thus, Applied Geology from the while the impact theory is re-emerging, available evidence University of Saugar and has been with the is still insufficient to rule out either of the two hypotheses. Geological Survey of India since 1974. His interests Introduction include geochemistry, petrology and palae oceanography. He is It is now widely believed that life on earth began very early in presently posted to the its geological history, probably about 4000 My (million years) Marine Wing of the ago (Mojzsis and others, 1996). Since then it underwent Department and has participated in many several evolutionary branchings to the complex diversity as scientific cruises both as we see today. Nevertheless, it was not a smooth voyage for life Chief Scientist and as a all along, the evolution was punctuated by geologically participating scientist. ins tan taneous events of mass mortality. New species emerged at the expense of their predecessors following each extinction event and life went on evolving ever more vibrantly. In the geologic record of rock strata, such mass extinction events are identifiable based on sudden absence and reduction in diversity of fossil assemblage across stratigraphic boundaries. -
(Diapsida: Saurosphargidae), with Implications for the Morphological Diversity and Phylogeny of the Group
Geol. Mag.: page 1 of 21. c Cambridge University Press 2013 1 doi:10.1017/S001675681300023X A new species of Largocephalosaurus (Diapsida: Saurosphargidae), with implications for the morphological diversity and phylogeny of the group ∗ CHUN LI †, DA-YONG JIANG‡, LONG CHENG§, XIAO-CHUN WU†¶ & OLIVIER RIEPPEL ∗ Laboratory of Evolutionary Systematics of Vertebrates, Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences, PO Box 643, Beijing 100044, China ‡Department of Geology and Geological Museum, Peking University, Beijing 100871, PR China §Wuhan Institute of Geology and Mineral Resources, Wuhan, 430223, PR China ¶Canadian Museum of Nature, PO Box 3443, STN ‘D’, Ottawa, ON K1P 6P4, Canada Department of Geology, The Field Museum, 1400 S. Lake Shore Drive, Chicago, IL 60605-2496, USA (Received 31 July 2012; accepted 25 February 2013) Abstract – Largocephalosaurus polycarpon Cheng et al. 2012a was erected after the study of the skull and some parts of a skeleton and considered to be an eosauropterygian. Here we describe a new species of the genus, Largocephalosaurus qianensis, based on three specimens. The new species provides many anatomical details which were described only briefly or not at all in the type species, and clearly indicates that Largocephalosaurus is a saurosphargid. It differs from the type species mainly in having three premaxillary teeth, a very short retroarticular process, a large pineal foramen, two sacral vertebrae, and elongated small granular osteoderms mixed with some large ones along the lateral most side of the body. With additional information from the new species, we revise the diagnosis and the phylogenetic relationships of Largocephalosaurus and clarify a set of diagnostic features for the Saurosphargidae Li et al. -
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, -
Fossil Middle Triassic “Sea Cows” – Placodont Reptiles As Macroalgae Feeders Along the North-Western Tethys Coastline with Pangaea and in the Germanic Basin
Vol.3, No.1, 9-27 (2011) Natural Science http://dx.doi.org/10.4236/ns.2011.31002 Fossil middle triassic “sea cows” – placodont reptiles as macroalgae feeders along the north-western Tethys coastline with Pangaea and in the Germanic basin Cajus G. Diedrich Paleologic, Nansenstr, Germany; [email protected] Received 19 October 2010; revised 22 November 2010; accepted 27 November 2010. ABSTRACT this plant-feeding adaptation and may even ex- plain the origin or at least close relationship of The descriptions of fossil Triassic marine pla- the earliest Upper Triassic turtles as toothless codonts as durophagous reptiles are revised algae and jellyfish feeders, in terms of the through comparisons with the sirenia and basal long-term convergent development with the si- proboscidean mammal and palaeoenvironment rens. analyses. The jaws of placodonts are conver- gent with those of Halitherium/Dugong or Mo- Keywords: Placodont Reptiles; Triassic; eritherium in their general function. Whereas Convergent Evolutionary Ecological Adaptation; Halitherium possessed a horny oral pad and Sirenia; Macroalgae Feeders; NW Tethys Shelf; counterpart and a special rasp-like tongue to Palaeoecology grind seagrass, as does the modern Dugong, placodonts had large teeth that covered their 1. INTRODUCTION jaws to form a similar grinding pad. The sirenia also lost their anterior teeth during many Mil- The extinct reptile group of the placodonts found in lions of years and built a horny pad instead and Germany and other European sites (Figure 1), a group specialized tongue to fed mainly on seagrass, of diverse marine diving reptiles, had large teeth cover- whereas placodonts had only macroalgae availa- ing the lower and complete upper jaws (Figsure 2-5) ble. -
Cretaceous Fossils from the Chesapeake and Delaware Canal
Cretaceous S;cial Publication No. 18 Fossils from the Chesapeake and Delaware Canal A Guide for Students and Collectors Edward M. Lauginiger / /~ / CRETACEOUS FOSSILS FROM THE CHESAPEAKE AND DELAWARE CANAL: A GUIDE FOR STUDENTS AND COLLECTORS By Edward M. Lauginiger Biology Teacher Academy Park High School Sharon Hill, Pennsylvania September 1988 Reprinted 1997 CONTENTS Page INTRODUCTION. • 1 ACKNOWLEDGMENTS 2 PREVIOUS STUDIES. 3 FOSSILS AND FOSSILIZATION 5 Requirements for Fossilization 6 Types of Fossilization 7 GEOLOGY •• 10 CLASSIFICATON OF FOSSILS. 12 Kingdom Monera • 13 Kindgom Protista 1 3 Kingdom Plantae. 1 4 Kingdom Animalia 15 Phylum Porifera 15 Phylum Cnidaria (Coelenterata). 16 Phylum Bryozoa. 16 Phylum Brachiopoda. 17 Phylum Mollusca • 18 Phylum Annelida •. 22 Phylum Arthropoda • 23 Phylum Echinodermata. 24 Phylum Chordata 24 COLLECTING LOCALITIES 28 FOSSIL CHECK LIST 30 BIBLIOGRAPHY. 33 PLATES. ••• 39 iii FIGURES Page Figure 1 • Index map of the Chesapeake and Delaware Canal Area. .. .. 2 Figure 2. Generalized stratigraphic column of the formations exposed at the C & D Canal. 11 Figure 3. Foraminifera 14 Figure 4. Porifera 16 Figure 5. Cnidaria 16 Figure 6. Bryozoa. 17 Figure 7. Brachiopoda. 18 Figure 8. Mollusca-Gastropoda. 19 Figure 9. Mollusca-Pelecypoda. 21 Figure 10. Mollusca-Cephalopoda 22 Figure 11. Annelida . 22 Figure 12. Arthropoda 23 Figure 13. Echinodermata. 25 Figure 1 4. Chordata . 27 Figure 1 5. Collecting localities at the Chesapeake and Delaware Canal . ... .. 29 v CRETACEOUS FOSSILS FROM THE CHESAPEAKE AND DELAWARE CANAL: A GUIDE FOR STUDENTS AND COLLECTORS Edward M. Lauginiger INTRODUCTION Fossil collectors have been attracted to Delaware since the late 1820s when the excavation of the Chesapeake and Delaware (C&D) Canal first exposed marine fossils of Cretaceous age (Fig. -
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............................................................................................................................................................... -
Tesis Doctoral 2018
TESIS DOCTORAL 2018 HISTORIA EVOLUTIVA DE SIMOSAURIDAE (SAUROPTERYGIA). CONTEXTO SISTEMÁTICO Y BIOGEOGRÁFICO DE LOS REPTILES MARINOS DEL TRIÁSICO DE LA PENÍNSULA IBÉRICA CARLOS DE MIGUEL CHAVES PROGRAMA DE DOCTORADO EN CIENCIAS FRANCISCO ORTEGA COLOMA ADÁN PÉREZ GARCÍA RESUMEN Los sauropterigios fueron un exitoso grupo de reptiles marinos que vivió durante el Mesozoico, apareciendo en el Triásico Inferior y desapareciendo a finales del Cretácico Superior. Este grupo alcanzó su máxima disparidad conocida durante el Triásico Medio e inicios del Triásico Superior, diversificándose en numerosos grupos con distintos modos de vida y adaptaciones tróficas. El registro fósil de este grupo durante el Triásico es bien conocido a nivel global, habiéndose hallado abundantes restos en Norteamérica, Europa, el norte de África, Oriente Próximo y China. A pesar del relativamente abundante registro de sauropterigios triásicos ibéricos, los restos encontrados son, por lo general, elementos aislados y poco informativos a nivel sistemático en comparación con los de otros países europeos como Alemania, Francia o Italia. En la presente tesis doctoral se realiza una puesta al día sobre el registro ibérico triásico de Sauropterygia, con especial énfasis en el clado Simosauridae, cuyo registro ibérico permanecía hasta ahora inédito. Además de la revisión de ejemplares de sauropterigios previamente conocidos, se estudian numerosos ejemplares inéditos. De esta manera, se evalúan hipótesis previas sobre la diversidad peninsular de este clado y se reconocen tanto formas definidas en otras regiones europeas y de Oriente Próximo, pero hasta ahora no identificadas en la península ibérica, como nuevos taxones. La definición de nuevas formas y el incremento de la información sobre otras previamente conocidas permiten la propuesta de hipótesis filogenéticas y la redefinición de varios taxones. -
A Fast-Growing Basal Troodontid (Dinosauria: Theropoda) from The
www.nature.com/scientificreports OPEN A fast‑growing basal troodontid (Dinosauria: Theropoda) from the latest Cretaceous of Europe Albert G. Sellés1,2*, Bernat Vila1,2, Stephen L. Brusatte3, Philip J. Currie4 & Àngel Galobart1,2 A characteristic fauna of dinosaurs and other vertebrates inhabited the end‑Cretaceous European archipelago, some of which were dwarves or had other unusual features likely related to their insular habitats. Little is known, however, about the contemporary theropod dinosaurs, as they are represented mostly by teeth or other fragmentary fossils. A new isolated theropod metatarsal II, from the latest Maastrichtian of Spain (within 200,000 years of the mass extinction) may represent a jinfengopterygine troodontid, the frst reported from Europe. Comparisons with other theropods and phylogenetic analyses reveal an autapomorphic foramen that distinguishes it from all other troodontids, supporting its identifcation as a new genus and species, Tamarro insperatus. Bone histology shows that it was an actively growing subadult when it died but may have had a growth pattern in which it grew rapidly in early ontogeny and attained a subadult size quickly. We hypothesize that it could have migrated from Asia to reach the Ibero‑Armorican island no later than Cenomanian or during the Maastrichtian dispersal events. During the latest Cretaceous (ca. 77–66 million years ago) in the run-up to the end-Cretaceous mass extinc- tion, Europe was a series of islands populated by diverse and distinctive communities of dinosaurs and other vertebrates. Many of these animals exhibited peculiar features that may have been generated by lack of space and resources in their insular habitats. -
Educator Guide
Educator Guide BACKGROUND INFORMATION Welcome to the world of the late Cretaceous Period, filled with huge carnivorous marine reptiles with double-hinged jaws and teeth in the middle of their palates. Come see gigantic flesh-eating fish big enough to swallow an adult human being whole, flying reptiles with 3-foot skulls, and the biggest sea turtles to have ever lived. Many bizarre and gigantic forms of life populated the prehistoric waters of the late Cretaceous Period. The Midwest was actually underwater at one time. Kansas has only been above sea level for the last 65 million years. Before that, it was home to a variety of sea creatures, including a 45-foot long mosasaur, a sea turtle the size of a small truck, a giant carnivorous fish, and a long-necked plesiosaur. Although these prehistoric marine animals lived during the time of Tyrannosaurus and Triceratops, they are not dinosaurs. Dinosaurs lived on land and did not have wings for flying or fins for swimming. Many Cretaceous marine fossils have been found in Western Kansas. These fossils have been found in thousands of feet of marine sediments made up of shale, chalk, limestone, and sandstone. Common Questions When was the Cretaceous period? The Cretaceous Period extended from 144 to 65 million years ago. What is a mosasaur? A mosasaur is a large marine lizard with a long body and paddle-like limbs. Mosasaurs are not dinosaurs. The chief feature that distinguishes them from dinosaurs is the great flexibility and power of their jaws. Unlike most monstrous reptiles of the past, they still have living relatives, the giant monitor lizards such as the Komodo Dragons.