Cetaceans with Two Dorsal Fins
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The Wingtips of the Pterosaurs: Anatomy, Aeronautical Function and Palaeogeography, Palaeoclimatology, Palaeoecology Xxx (2015) Xxx Xxx 3 Ecological Implications
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Sea Monsters and Real Environmental Threats: Reconsidering the Famous Osborne, ‘Moha-Moha’, Valhalla, and ‘Soay Beast’ Sightings of Unidentified Marine Objects
IMAGINARY SEA MONSTERS AND REAL ENVIRONMENTAL THREATS: RECONSIDERING THE FAMOUS OSBORNE, ‘MOHA-MOHA’, VALHALLA, AND ‘SOAY BEAST’ SIGHTINGS OF UNIDENTIFIED MARINE OBJECTS R. L. FRANCE Dal Ocean Research Group Department of Plant, Food, and Environmental Sciences, Dalhousie University Abstract At one time, largely but not exclusively during the nineteenth century, retellings of encounters with sea monsters were a mainstay of dockside conversations among mariners, press reportage for an audience of fascinated landlubbers, and journal articles published by believing or sceptical natural scientists. Today, to the increasing frustration of cryptozoologists, mainstream biologists and environmental historians have convincingly argued that there is a long history of conflating or misidentifying known sea animals as purported sea monsters. The present paper provides, for the first time, a detailed, diachronic review of competing theories that have been posited to explain four particular encounters with sea monsters, which at the time of the sightings (1877, 1890, 1905, and 1959) had garnered worldwide attention and considerable fame. In so doing, insights are gleaned about the role played by sea monsters in the culture of late-Victorian natural science. Additionally, and most importantly, I offer my own parsimonious explanation that the observed ‘sea monsters’ may have been sea turtles entangled in pre-plastic fishing gear or maritime debris. Environmental history is therefore shown to be a valuable tool for looking backward in order to postulate the length of time that wildlife populations have been subjected to anthropogenic pressure. This is something of contemporary importance, given that scholars are currently involved in deliberations concerning the commencement date of the Anthropocene Era. -
Evolutionary History of the Porpoises
bioRxiv preprint doi: https://doi.org/10.1101/851469; this version posted November 22, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Evolutionary history of the porpoises (Phocoenidae) across the 2 speciation continuum: a mitogenome phylogeographic perspective 3 4 Yacine Ben Chehida1, Julie Thumloup1, Cassie Schumacher2, Timothy Harkins2, Alex 5 Aguilar3, Asunción Borrell3, Marisa Ferreira4, Lorenzo Rojas-Bracho5, Kelly M. Roberston6, 6 Barbara L. Taylor6, Gísli A. Víkingsson7, Arthur Weyna8, Jonathan Romiguier8, Phillip A. 7 Morin6, Michael C. Fontaine1,9* 8 9 1 Groningen Institute for Evolutionary Life Sciences (GELIFES), University of Groningen, PO Box 11103 CC, 10 Groningen, The Netherlands 11 2 Swift Biosciences, 674 S. Wagner Rd., Suite 100, Ann Arbor, MI 48103, USA 12 3 IRBIO and Department of Evolutive Biology, Ecology and Environmental Sciences, Faculty of Biology, 13 University of Barcelona, Diagonal 643, 08071 Barcelona, Spain 14 4 MATB-Sociedade Portuguesa de Vida Selvagem, Estação de Campo de Quiaios, Apartado EC Quiaios, 3080- 15 530 Figueira da Foz, Portugal & CPRAM-Ecomare, Estrada do Porto de Pesca Costeira, 3830-565 Gafanha da 16 Nazaré, Portugal 17 5 Instituto Nacional de Ecología, Centro de Investigación Científica y de Educación Superior de Ensenada, 18 Carretera Ensenada-Tijuana 3918, Fraccionamiento Zona Playitas, Ensenada, BC 22860, Mexico 19 6 Southwest Fisheries Science Center, National Marine Fisheries Service, NOAA, 8901 La Jolla Shores Dr., La 20 Jolla, California 92037, USA 21 7 Marine and Freshwater Research Institute, PO Box 1390, 121 Reykjavik, Iceland 22 8 Institut des Sciences de l’Évolution (Université de Montpellier, CNRS UMR 5554), Montpellier, France 23 9 Laboratoire MIVEGEC (Université de Montpellier, UMR CNRS 5290, IRD 229), Centre IRD de Montpellier, 24 Montpellier, France 25 26 *Corresponding author: Michael C. -
Median Fin Patterning in Bony Fish: Caspase-3 Role in Fin Fold Reabsorption
Eastern Illinois University The Keep Undergraduate Honors Theses Honors College 2017 Median Fin Patterning in Bony Fish: Caspase-3 Role in Fin Fold Reabsorption Kaitlyn Ann Hammock Follow this and additional works at: https://thekeep.eiu.edu/honors_theses Part of the Animal Sciences Commons Median fin patterning in bony fish: caspase-3 role in fin fold reabsorption BY Kaitlyn Ann Hammock UNDERGRADUATE THESIS Submitted in partial fulfillment of the requirement for obtaining UNDERGRADUATE DEPARTMENTAL HONORS Department of Biological Sciences along with the HonorsCollege at EASTERN ILLINOIS UNIVERSITY Charleston, Illinois 2017 I hereby recommend this thesis to be accepted as fulfilling the thesis requirement for obtaining Undergraduate Departmental Honors Date '.fHESIS ADVI 1 Date HONORSCOORDmATOR f C I//' ' / ·12 1' J Date, , DEPARTME TCHAIR Abstract Fish larvae develop a fin fold that will later be replaced by the median fins. I hypothesize that finfold reabsorption is part of the initial patterning of the median fins,and that caspase-3, an apoptosis marker, will be expressed in the fin fold during reabsorption. I analyzed time series of larvae in the first20-days post hatch (dph) to determine timing of median findevelopment in a basal bony fish- sturgeon- and in zebrafish, a derived bony fish. I am expecting the general activation pathway to be conserved in both fishesbut, the timing and location of cell death to differ.The dorsal fin foldis the firstto be reabsorbed in the sturgeon starting at 2 dph and rays formed at 6dph. This was closely followed by the anal finat 3 dph, rays at 9 dph and only later, at 6dph, does the caudal fin start forming and rays at 14 dph. -
FC Inshore Cetacean Species Identification
Falklands Conservation PO BOX 26, Falkland Islands, FIQQ 1ZZ +500 22247 [email protected] www.falklandsconservation.com FC Inshore Cetacean Species Identification Introduction This guide outlines the key features that can be used to distinguish between the six most common cetacean species that inhabit Falklands' waters. A number of additional cetacean species may occasionally be seen in coastal waters, for example the fin whale (Balaenoptera physalus), the humpback whale (Megaptera novaeangliae), the long-finned pilot whale (Globicephala melas) and the dusky dolphin (Lagenorhynchus obscurus). A full list of the species that have been documented to date around the Falklands can be found in Appendix 1. Note that many of these are typical of deeper, oceanic waters, and are unlikely to be encountered along the coast. The six species (or seven species, including two species of minke whale) described in this document are observed regularly in shallow, nearshore waters, and are the focus of this identification guide. Questions and further information For any questions about species identification then please contact the Cetaceans Project Officer Caroline Weir who will be happy to help you try and identify your sighting: Tel: 22247 Email: [email protected] Useful identification guides If you wish to learn more about the identification features of various species, some comprehensive field guides (which include all cetacean species globally) include: Handbook of Whales, Dolphins and Porpoises by Mark Carwardine. 2019. Marine Mammals of the World: A Comprehensive Guide to Their Identification by Thomas A. Jefferson, Marc A. Webber, and Robert L. Pitman. 2015. Whales, Dolphins and Seals: A Field Guide to the Marine Mammals of the World by Hadoram Shirihai and Brett Jarrett. -
Human Functional Anatomy 213 the Upper Limb Early Limb Development
2 HUMAN FUNCTIONAL ANATOMY 213 THE UPPER LIMB EARLY LIMB DEVELOPMENT THIS WEEKS LAB: IN THE FISH (or early human embryo) Proximal parts, plexuses and patterns Slight elevations of ectoderm appear in lateral plate (4th week). Apical ectodermal ridge induces proliferation of limb mesenchyme. READINGS Dorsal and ventral muscle masses connect the girdle to the limb bud. Stern. Essentials of Gross anatomy – The upper limb Limb girdle in body wall Stern. Core concepts in Anatomy:- 80: Organization of upper limb musculature and the Proximal, middle and distal segments of the limb brachial plexus Faiz and Moffat. Anatomy at a Glance:- Nerves of the Upper limb 1 & 2 (parts 30 &31) Grant's Method:- Upper limb and Back (especially pectoral region and axilla) OR any other regional textbook - similar sections IN THIS LECTURE I WILL COVER: Ontogeny and Phylogeny The Pectoral fin The primitive tetrapod forelimb Rotations of the limb in phylogeny Dorsal and ventral muscle/nerve/girdle bone Segmental nerve supply and muscle groups Brachial plexus Muscle groups of the upper limb The fin, or paddle has: Preaxial and postaxial borders (front and back edges) Dorsal and ventral surfaces (top and bottom) Dorsal muscles elevate the fin. Attach to dorsal elements of the girdle (“scapula” and vertebrae) Ventral muscles depress the fin. Attach to ventral elements of the girdle (coracoid) 3 4 PRIMITIVE TETRAPOD FORELIMB MAMMALIAN FORELIMB ROTATIONS 90 degrees LATERAL ROTATION The characteristic segments of the limb (shoulder, arm, forearm, & hand) Were present in -
How to Tell a Sea Monster: Molecular Discrimination of Large Marine Animals of the North Atlantic
Reference: Biol. Bull. 202: 1–5. (February 2002) How To Tell a Sea Monster: Molecular Discrimination of Large Marine Animals of the North Atlantic S. M. CARR1,*, H. D. MARSHALL1, K. A. JOHNSTONE1, L. M. PYNN1, AND G. B. STENSON2 1Genetics, Evolution, and Molecular Systematics Laboratory, Department of Biology, Memorial University of Newfoundland, St. John’s, Newfoundland A1B 3X9, Canada; and 2Marine Mammals Section, Science, Oceans, and Environment Branch, Department of Fisheries and Oceans, PO Box 5667, St. John’s, Newfoundland A1C 5X1, Canada “Either we do know all the varieties of beings which people our planet, or we do not. If we do not know them all—if Nature has still secrets in the deeps for us, nothing is more conformable to reason than to admit the existence of fishes, or cetaceans of other kinds, or even of new species ...which an accident of some sort has brought at long intervals to the upper level of the ocean.” —Jules Verne, Twenty Thousand Leagues Under the Sea, 1870 Abstract. Remains of large marine animals that wash (1994) gives a contemporary list. Even in the first year of a onshore can be difficult to identify due to decomposition new century when the complete human genome has become and loss of external body parts, and in consequence may be known (International Human Genome Sequencing Consor- dubbed “sea monsters.” DNA that survives in such car- tium, 2001), the possibility that entirely new, previously casses can provide a basis of identification. One such crea- unknown species may unexpectedly present themselves re- ture washed ashore at St. -
Re-Evaluation of Pachycormid Fishes from the Late Jurassic of Southwestern Germany
Editors' choice Re-evaluation of pachycormid fishes from the Late Jurassic of Southwestern Germany ERIN E. MAXWELL, PAUL H. LAMBERS, ADRIANA LÓPEZ-ARBARELLO, and GÜNTER SCHWEIGERT Maxwell, E.E., Lambers, P.H., López-Arbarello, A., and Schweigert G. 2020. Re-evaluation of pachycormid fishes from the Late Jurassic of Southwestern Germany. Acta Palaeontologica Polonica 65 (3): 429–453. Pachycormidae is an extinct group of Mesozoic fishes that exhibits extensive body size and shape disparity. The Late Jurassic record of the group is dominated by fossils from the lithographic limestone of Bavaria, Germany that, although complete and articulated, are not well characterized anatomically. In addition, stratigraphic and geographical provenance are often only approximately known, making these taxa difficult to place in a global biogeographical context. In contrast, the late Kimmeridgian Nusplingen Plattenkalk of Baden-Württemberg is a well-constrained locality yielding hundreds of exceptionally preserved and prepared vertebrate fossils. Pachycormid fishes are rare, but these finds have the potential to broaden our understanding of anatomical variation within this group, as well as provide new information regarding the trophic complexity of the Nusplingen lagoonal ecosystem. Here, we review the fossil record of Pachycormidae from Nusplingen, including one fragmentary and two relatively complete skulls, a largely complete fish, and a fragment of a caudal fin. These finds can be referred to three taxa: Orthocormus sp., Hypsocormus posterodorsalis sp. nov., and Simocormus macrolepidotus gen. et sp. nov. The latter taxon was erected to replace “Hypsocormus” macrodon, here considered to be a nomen dubium. Hypsocormus posterodorsalis is known only from Nusplingen, and is characterized by teeth lacking apicobasal ridging at the bases, a dorsal fin positioned opposite the anterior edge of the anal fin, and a hypural plate consisting of a fused parhypural and hypurals. -
From Fin to Forelimb Crucially Showing That They Develop in Situ Rather Than Migrating to Their the Vertebrate Invasion of Land Was Cartilaginous Fish Such As Sharks
NATURE|Vol 466|5 August 2010 NEWS & VIEWS Goulielmakis and colleagues1 characterized Figure 1 | The first attosecond probe the coherence, and thus the entanglement, of experiments. Goulielmakis et al.1 report a Kr+ and the lost electron. In their experiments, technique for observing electron motion in the intense, ultrashort pump pulse ensures real time. They irradiated krypton atoms (Kr) significant overlap of the two quantum states Kr+, 3d–1 with a ‘pump’ pulse of infrared light lasting a few femtoseconds, liberating electrons to of the removed electron that correlate with generate Kr+ ions in a superposition of two two different pathways in the ion’s subsystem states, 4p−1(J = 1/2) and 4p−1(J = 3/2), where J is (Fig. 1b), resulting in a low electron–ion entan- total angular momentum. Black arrows indicate glement, a high coherence of the hole’s wave the two ionization pathways. The authors then packet and high visibility of the interference Kr+, irradiated the ions with attosecond ‘probe’ pulses 4p–1(J=1/2) fringes. The ability to probe decoherence is a + of extreme-ultraviolet light, exciting them to a Kr , −1 very important aspect of the experiment. 4p–1(J=3/2) higher-energy 3d state; red and green arrows The authors’ experiment is reminiscent of a indicate the two possible excitation pathways. two-colour coherent-control scheme2. In such The complete system constitutes an entangled electron–ion pair. a, The different excitation schemes, population of a final state is controlled pathways taken by the ion to reach the 3d−1 by the relative phase between the two colours state may cause the liberated electrons to adopt of light needed to promote a system from two orthogonal quantum states. -
Alexander 2013 Principles-Of-Animal-Locomotion.Pdf
.................................................... Principles of Animal Locomotion Principles of Animal Locomotion ..................................................... R. McNeill Alexander PRINCETON UNIVERSITY PRESS PRINCETON AND OXFORD Copyright © 2003 by Princeton University Press Published by Princeton University Press, 41 William Street, Princeton, New Jersey 08540 In the United Kingdom: Princeton University Press, 3 Market Place, Woodstock, Oxfordshire OX20 1SY All Rights Reserved Second printing, and first paperback printing, 2006 Paperback ISBN-13: 978-0-691-12634-0 Paperback ISBN-10: 0-691-12634-8 The Library of Congress has cataloged the cloth edition of this book as follows Alexander, R. McNeill. Principles of animal locomotion / R. McNeill Alexander. p. cm. Includes bibliographical references (p. ). ISBN 0-691-08678-8 (alk. paper) 1. Animal locomotion. I. Title. QP301.A2963 2002 591.47′9—dc21 2002016904 British Library Cataloging-in-Publication Data is available This book has been composed in Galliard and Bulmer Printed on acid-free paper. ∞ pup.princeton.edu Printed in the United States of America 1098765432 Contents ............................................................... PREFACE ix Chapter 1. The Best Way to Travel 1 1.1. Fitness 1 1.2. Speed 2 1.3. Acceleration and Maneuverability 2 1.4. Endurance 4 1.5. Economy of Energy 7 1.6. Stability 8 1.7. Compromises 9 1.8. Constraints 9 1.9. Optimization Theory 10 1.10. Gaits 12 Chapter 2. Muscle, the Motor 15 2.1. How Muscles Exert Force 15 2.2. Shortening and Lengthening Muscle 22 2.3. Power Output of Muscles 26 2.4. Pennation Patterns and Moment Arms 28 2.5. Power Consumption 31 2.6. Some Other Types of Muscle 34 Chapter 3. -
N: a Sea Monster of a Research Project
Utah State University DigitalCommons@USU Undergraduate Honors Capstone Projects Honors Program 5-2019 N: A Sea Monster of a Research Project Adrian Jay Thomson Utah State University Follow this and additional works at: https://digitalcommons.usu.edu/honors Part of the English Language and Literature Commons Recommended Citation Thomson, Adrian Jay, "N: A Sea Monster of a Research Project" (2019). Undergraduate Honors Capstone Projects. 424. https://digitalcommons.usu.edu/honors/424 This Thesis is brought to you for free and open access by the Honors Program at DigitalCommons@USU. It has been accepted for inclusion in Undergraduate Honors Capstone Projects by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. N: A SEA MONSTER OF A RESEARCH PROJECT by Adrian Jay Thomson Capstone submitted in partial fulfillment of the requirements for graduation with UNIVERSITY HONORS with a major in English- Creative Writing in the Department of English Approved: UTAH STATE UNIVERSITY Logan, UT SPRING2019 Abstract Ever since time and the world began, dwarves have always fought cranes. Ever since ships set out on the northern sea, great sea monsters have risen to prey upon them. Such are the basics of life in medieval and Renaissance Scandinavia , Iceland, Scotland and Greenland, as detailed by Olaus Magnus' Description of the Northern Peoples (1555) , its sea monster -heavy map , the Carta Marina (1539), and Abraham Ortelius' later map of Iceland, Islandia (1590). I first learned of Olaus and Ortelius in the summer of 2013 , and while drawing my own version of their sea monster maps a thought hit me: write a book series , with teenage characters similar to those in How to Train Your Dragon , but set it amongst the lands described by Olaus , in a frozen world badgered by the sea monsters of Ortelius. -
Tetrapod Limb and Sarcopterygian Fin Regeneration Share a Core Genetic
ARTICLE Received 28 Apr 2016 | Accepted 27 Sep 2016 | Published 2 Nov 2016 DOI: 10.1038/ncomms13364 OPEN Tetrapod limb and sarcopterygian fin regeneration share a core genetic programme Acacio F. Nogueira1,*, Carinne M. Costa1,*, Jamily Lorena1, Rodrigo N. Moreira1, Gabriela N. Frota-Lima1, Carolina Furtado2, Mark Robinson3, Chris T. Amemiya3,4, Sylvain Darnet1 & Igor Schneider1 Salamanders are the only living tetrapods capable of fully regenerating limbs. The discovery of salamander lineage-specific genes (LSGs) expressed during limb regeneration suggests that this capacity is a salamander novelty. Conversely, recent paleontological evidence supports a deeper evolutionary origin, before the occurrence of salamanders in the fossil record. Here we show that lungfishes, the sister group of tetrapods, regenerate their fins through morphological steps equivalent to those seen in salamanders. Lungfish de novo transcriptome assembly and differential gene expression analysis reveal notable parallels between lungfish and salamander appendage regeneration, including strong downregulation of muscle proteins and upregulation of oncogenes, developmental genes and lungfish LSGs. MARCKS-like protein (MLP), recently discovered as a regeneration-initiating molecule in salamander, is likewise upregulated during early stages of lungfish fin regeneration. Taken together, our results lend strong support for the hypothesis that tetrapods inherited a bona fide limb regeneration programme concomitant with the fin-to-limb transition. 1 Instituto de Cieˆncias Biolo´gicas, Universidade Federal do Para´, Rua Augusto Correa, 01, Bele´m66075-110,Brazil.2 Unidade Genoˆmica, Programa de Gene´tica, Instituto Nacional do Caˆncer, Rio de Janeiro 20230-240, Brazil. 3 Benaroya Research Institute at Virginia Mason, 1201 Ninth Avenue, Seattle, Washington 98101, USA. 4 Department of Biology, University of Washington 106 Kincaid, Seattle, Washington 98195, USA.