A Petition to List the Insular Population of Hawaiian False Killer Whale (Pseudorca Crassidens) As Endangered Under the Endangered Species Act
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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 The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.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. -
THE CASE AGAINST Marine Mammals in Captivity Authors: Naomi A
s l a m m a y t T i M S N v I i A e G t A n i p E S r a A C a C E H n T M i THE CASE AGAINST Marine Mammals in Captivity The Humane Society of the United State s/ World Society for the Protection of Animals 2009 1 1 1 2 0 A M , n o t s o g B r o . 1 a 0 s 2 u - e a t i p s u S w , t e e r t S h t u o S 9 8 THE CASE AGAINST Marine Mammals in Captivity Authors: Naomi A. Rose, E.C.M. Parsons, and Richard Farinato, 4th edition Editors: Naomi A. Rose and Debra Firmani, 4th edition ©2009 The Humane Society of the United States and the World Society for the Protection of Animals. All rights reserved. ©2008 The HSUS. All rights reserved. Printed on recycled paper, acid free and elemental chlorine free, with soy-based ink. Cover: ©iStockphoto.com/Ying Ying Wong Overview n the debate over marine mammals in captivity, the of the natural environment. The truth is that marine mammals have evolved physically and behaviorally to survive these rigors. public display industry maintains that marine mammal For example, nearly every kind of marine mammal, from sea lion Iexhibits serve a valuable conservation function, people to dolphin, travels large distances daily in a search for food. In learn important information from seeing live animals, and captivity, natural feeding and foraging patterns are completely lost. -
Cetacea: Phocoenidae) from the Upper Part of the Horokaoshirarika Formation (Lower Pliocene), Numata Town, Hokkaido, Japan, and Its Phylogenetic Position
Palaeontologia Electronica palaeo-electronica.org A new skull of the fossil porpoise Numataphocoena yamashitai (Cetacea: Phocoenidae) from the upper part of the Horokaoshirarika Formation (lower Pliocene), Numata Town, Hokkaido, Japan, and its phylogenetic position Yoshihiro Tanaka and Hiroto Ichishima ABSTRACT An early Pliocene porpoise, Numataphocoena yamashitai from Hokkaido, Japan, is known from the holotype, a fairly well-preserved skeleton with an incomplete skull and a referred earbone. A new skull referred to Numataphocoena yamashitai found from almost the same locality as the holotype is interesting because it expands knowl- edge of skull morphology and improves the diagnosis of this taxon. Numataphocoena yamashitai differs from other phocoenids in having the characteristic feature in the maxilla associated with the posterior dorsal infraorbital foramen, narrower and sharper anterior part of the internal acoustic meatus, and a robust anterior process of the peri- otic. A new cladistic analysis places Numataphocoena yamashitai adjacent to Haboro- phocoena toyoshimai and Haborophocoena minutus, among a clade of early branching phocoenids, all of which are chronologically and geographically close to each other. The new skull is probably a younger individual because it is about 80% the size of that of the holotype and it shows closed but unfused sutures. Our description of this specimen helps to understand the intraspecies variation of the extinct species Numataphocoena yamashitai. Yoshihiro Tanaka. Numata Fossil Museum, 2-7-49, Minami 1, Numata Town, Hokkaido, 078-2225 Japan, [email protected] and Hokkaido University Museum, Kita 10, Nishi 8, Kita-ku, Sapporo, Hokkaido 060-0810 Japan Hiroto Ichishima. Fukui Prefectural Dinosaur Museum, Terao 51-11, Muroko, Katsuyama, Fukui 911-8601, Japan, [email protected] Key words: skull; Phocoenidae; phylogeny; maxillary terrace; ontogeny; intraspecies variation Submission: 22 March 2016 Acceptance: 20 October 2016 Tanaka, Yoshihiro and Ichishima, Hiroto. -
Pseudorca Crassidens) and Nine Other Odontocete Species from Hawai‘I
Ecotoxicology DOI 10.1007/s10646-014-1300-0 Cytochrome P4501A1 expression in blubber biopsies of endangered false killer whales (Pseudorca crassidens) and nine other odontocete species from Hawai‘i Kerry M. Foltz • Robin W. Baird • Gina M. Ylitalo • Brenda A. Jensen Accepted: 2 August 2014 Ó Springer Science+Business Media New York 2014 Abstract Odontocetes (toothed whales) are considered insular false killer whale. Significantly higher levels of sentinel species in the marine environment because of their CYP1A1 were observed in false killer whales and rough- high trophic position, long life spans, and blubber that toothed dolphins compared to melon-headed whales, and in accumulates lipophilic contaminants. Cytochrome general, trophic position appears to influence CYP1A1 P4501A1 (CYP1A1) is a biomarker of exposure and expression patterns in particular species groups. No sig- molecular effects of certain persistent organic pollutants. nificant differences in CYP1A1 were found based on age Immunohistochemistry was used to visualize CYP1A1 class or sex across all samples. However, within male false expression in blubber biopsies collected by non-lethal killer whales, juveniles expressed significantly higher lev- sampling methods from 10 species of free-ranging els of CYP1A1 whenP compared to adults. Total polychlo- Hawaiian odontocetes: short-finned pilot whale, melon- rinated biphenyl ( PCBs) concentrations in 84 % of false headed whale, pygmy killer whale, common bottlenose killer whalesP exceeded proposed threshold levels for health dolphin, rough-toothed dolphin, pantropical spotted dol- effects, and PCBs correlated with CYP1A1 expression. phin, Blainville’s beaked whale, Cuvier’s beaked whale, There was no significant relationship between PCB toxic sperm whale, and endangered main Hawaiian Islands equivalent quotient and CYP1A1 expression, suggesting that this response may be influenced by agonists other than the dioxin-like PCBs measured in this study. -
MHI Insular False Killer Whale Species Status Assessment
Recovery Status Review Pacific Islands for the Regional Office Protected Resources Main Hawaiian Islands Insular False Killer Whale Distinct Population Segment August 2020 (Version 1.0) Cover photo by Robin Baird, Cascadia Research Collective. RECOVERY STATUS REVIEW | Main Hawaiian Islands Insular False Killer Whale DPS Page ii Contents EXECUTIVE SUMMARY ........................................................................................................... v LIST OF FIGURES .................................................................................................................. viii LIST OF TABLES ..................................................................................................................... ix LIST OF BOXES ....................................................................................................................... ix LIST OF TERMS, ABBREVIATIONS, AND ACRONYMS ................................................................. x 1 INTRODUCTION ..................................................................................................... 1–1 1.1 History of the Main Hawaiian Islands Insular False Killer Whale ESA Listing and Recovery Planning ..................................................................................................... 1–1 1.2 Distinct Population Segment Overview ..................................................................... 1–2 1.3 Approach to the Recovery Status Review ................................................................. 1–2 2 SPECIES INFORMATION -
Phylogeny of All Major Groups of Cetaceans Based on DNA Sequences from Three Mitochondrial Genes
Phylogeny of All Major Groups of Cetaceans Based on DNA Sequences from Three Mitochondrial Genes Michel C. Milinkovitch,* Axe1 Meyer) and Jeffrey R. Powell * *Department of Biology, Yale University and +Department of Ecology and Evolution, State University of New York at Stony Brook Traditionally, living cetaceans (order Cetacea) are classified into two highly distinct suborders: the echolocating toothed whales, Odontoceti, and the filter-feeding baleen whales, Mysticeti. A molecular phylogeny based on 1,352 base pairs of two mitochondrial ribosomal gene segments and the mitochondrial cytochrome b gene for all major groups of cetaceans contradicts this long-accepted taxonomic subdivision. One group of toothed whales, the sperm whales, is more closely related to the morphologically highly divergent baleen whales than to other odontocetes. This finding suggests that the suborder Odontoceti constitutes an unnatural grouping and challenges the conventional scenario of a long, independent evolutionary history of odontocetes and mysticetes. The superfamily Delphinoidea (dolphins, porpoises, and white whales) appears to be monophyletic; the Amazon River dolphin, Inia geofiensis, is its sister species. This river dolphin is genetically more divergent from the morphologically similar marine dolphins than the sperm whales are from the morphologically dissimilar baleen whales. The phylogenetic relationships among the three families of Delphinoidea remain uncertain, and we suggest that the two cladogenetic events that generated these three clades occurred within a very short period of time. Among the baleen whales, the bowhead is basal, and the gray whale is the sister species to the rorquals (family Balaenopteridae). The phylogenetic position of beaked whales (Ziphioidea) remains weakly supported by molecular data. -
Marine Mammal Taxonomy
Marine Mammal Taxonomy Kingdom: Animalia (Animals) Phylum: Chordata (Animals with notochords) Subphylum: Vertebrata (Vertebrates) Class: Mammalia (Mammals) Order: Cetacea (Cetaceans) Suborder: Mysticeti (Baleen Whales) Family: Balaenidae (Right Whales) Balaena mysticetus Bowhead whale Eubalaena australis Southern right whale Eubalaena glacialis North Atlantic right whale Eubalaena japonica North Pacific right whale Family: Neobalaenidae (Pygmy Right Whale) Caperea marginata Pygmy right whale Family: Eschrichtiidae (Grey Whale) Eschrichtius robustus Grey whale Family: Balaenopteridae (Rorquals) Balaenoptera acutorostrata Minke whale Balaenoptera bonaerensis Arctic Minke whale Balaenoptera borealis Sei whale Balaenoptera edeni Byrde’s whale Balaenoptera musculus Blue whale Balaenoptera physalus Fin whale Megaptera novaeangliae Humpback whale Order: Cetacea (Cetaceans) Suborder: Odontoceti (Toothed Whales) Family: Physeteridae (Sperm Whale) Physeter macrocephalus Sperm whale Family: Kogiidae (Pygmy and Dwarf Sperm Whales) Kogia breviceps Pygmy sperm whale Kogia sima Dwarf sperm whale DOLPHIN R ESEARCH C ENTER , 58901 Overseas Hwy, Grassy Key, FL 33050 (305) 289 -1121 www.dolphins.org Family: Platanistidae (South Asian River Dolphin) Platanista gangetica gangetica South Asian river dolphin (also known as Ganges and Indus river dolphins) Family: Iniidae (Amazon River Dolphin) Inia geoffrensis Amazon river dolphin (boto) Family: Lipotidae (Chinese River Dolphin) Lipotes vexillifer Chinese river dolphin (baiji) Family: Pontoporiidae (Franciscana) -
Review of Small Cetaceans. Distribution, Behaviour, Migration and Threats
Review of Small Cetaceans Distribution, Behaviour, Migration and Threats by Boris M. Culik Illustrations by Maurizio Wurtz, Artescienza Marine Mammal Action Plan / Regional Seas Reports and Studies no. 177 Published by United Nations Environment Programme (UNEP) and the Secretariat of the Convention on the Conservation of Migratory Species of Wild Animals (CMS). Review of Small Cetaceans. Distribution, Behaviour, Migration and Threats. 2004. Compiled for CMS by Boris M. Culik. Illustrations by Maurizio Wurtz, Artescienza. UNEP / CMS Secretariat, Bonn, Germany. 343 pages. Marine Mammal Action Plan / Regional Seas Reports and Studies no. 177 Produced by CMS Secretariat, Bonn, Germany in collaboration with UNEP Coordination team Marco Barbieri, Veronika Lenarz, Laura Meszaros, Hanneke Van Lavieren Editing Rüdiger Strempel Design Karina Waedt The author Boris M. Culik is associate Professor The drawings stem from Prof. Maurizio of Marine Zoology at the Leibnitz Institute of Wurtz, Dept. of Biology at Genova Univer- Marine Sciences at Kiel University (IFM-GEOMAR) sity and illustrator/artist at Artescienza. and works free-lance as a marine biologist. Contact address: Contact address: Prof. Dr. Boris Culik Prof. Maurizio Wurtz F3: Forschung / Fakten / Fantasie Dept. of Biology, Genova University Am Reff 1 Viale Benedetto XV, 5 24226 Heikendorf, Germany 16132 Genova, Italy Email: [email protected] Email: [email protected] www.fh3.de www.artescienza.org © 2004 United Nations Environment Programme (UNEP) / Convention on Migratory Species (CMS). This publication may be reproduced in whole or in part and in any form for educational or non-profit purposes without special permission from the copyright holder, provided acknowledgement of the source is made. -
Genetic Variation and Evidence for Population Structure in Eastern North Pacific False Killer Whales (Pseudorca Crassidens)
783 Genetic variation and evidence for population structure in eastern North Pacific false killer whales (Pseudorca crassidens) Susan J. Chivers, Robin W. Baird, Daniel J. McSweeney, Daniel L. Webster, Nicole M. Hedrick, and Juan Carlos Salinas Abstract: False killer whales (Pseudorca crassidens (Owen, 1846)) are incidentally taken in the North Pacific pelagic long-line fishery, but little is known about their population structure to assess the impact of these takes. Using mito- chondrial DNA (mtDNA) control region sequence data, we quantified genetic variation for the species and tested for genetic differentiation among geographic strata. Our data set of 124 samples included 115 skin-biopsy samples col- lected from false killer whales inhabiting the eastern North Pacific Ocean (ENP), and nine samples collected from ani- mals sampled at sea or on the beach in the western North Pacific, Indian, and Atlantic oceans. Twenty-four (24) haplotypes were identified, and nucleotide diversity was low ( = 0.37%) but comparable with that of closely related species. Phylogeographic concordance in the distribution of haplotypes was revealed and a demographically isolated population of false killer whales associated with the main Hawaiian islands was identified (ÈST = 0.47, p < 0.0001). This result supports recognition of the existing management unit, which has geo-political boundaries corresponding to the USA’s exclusive economic zone (EEZ) of Hawai‘i. However, a small number of animals sampled within the EEZ but away from the near-shore island area, which is defined as <25 nautical miles (1 nautical mile = 1.852 km) from shore, had haplotypes that were the same or closely related to those found elsewhere in the ENP, which suggests that there may be a second management unit within the Hawaiian EEZ. -
Pseudorca Crassidens (False Killer Whale)
UWI The Online Guide to the Animals of Trinidad and Tobago Behaviour Pseudorca crassidens (False Killer Whale) Family: Delphinidae (Oceanic Dolphins and Killer Whales) Order: Cetacea (Whales and Dolphins) Class: Mammalia (Mammals) Fig. 1. False killer whale, Pseudorca crassidens. [http://ocean.si.edu/ocean-photos/killer-whale-imposter, downloaded 31 October 2015] TRAITS. Pseudorca crassidens is at the upper size range within its family (Delphinidae); males can be as much as 6.1m and females 4.9m in head and body length (Nowak, 1999). Both sexes weigh in at around 700kg (NOAA Fisheries, 2013) although they can reach a maximum weight of 1360kg (Nowak, 1999). Newly born offspring are typically no longer than 1.8m and are only a fraction of an adult’s weight (Leatherwood, 1988). The false killer whale has a bulb or melon feature on its forehead (Fig. 1) which is slightly larger in males, and a narrow head which tapers into its slightly elongated and rounded snout. The jaws of P. crassidens hold 8-11 pairs of thick teeth and have an overhang, with the upper jaw protruding forward past the lower jaw. The thin sickle shaped dorsal fin of the false killer whale is also slightly tapered and can measure as much as 40cm tall (Leatherwood, 1988; Nowak, 1999). The pectoral flippers have a characteristic UWI The Online Guide to the Animals of Trinidad and Tobago Behaviour shape unique in its family, with a bulge on the front edge. Sexual dimorphism also occurs in the skull with size variation between male and female which measure 58-65cm and 55-59cm respectively. -
The Marine Mammal Captivity Issue: Time for a Paradigm Shift
In: The Palgrave Macmillan Series on Animal Ethics Edited by Andrew Linzey and Priscilla Cohn (in press) The Marine Mammal Captivity Issue: Time For a Paradigm Shift Lori Marino Dolphin and whale (cetacean) captivity is one of the most contentious cultural issues of modern times. Neither the “anti-“ or “pro-“ captivity groups can be expected to concede to the other but neither is it entirely impossible to conceive of ways to bring the two together over shared interests and objectives. So, the issue is whether there is a way to move forward into the future by combining forces for the benefit of everyone involved. In order to consider that possibility, three questions must be addressed. First, who are cetaceans? Second, do cetaceans flourish (or, thrive) in captivity? Third, what should we do about what we know about the answers to the first two questions? Scientific research done both in captivity and in the field has revealed much about who dolphins and whales are. There is no doubt that captive research has contributed substantially to our understanding of them. But that same empirical research leads to the inescapable conclusion that cetacean nature is fundamentally incompatible with captivity. Cetaceans cannot flourish in captivity. To flourish is to thrive and not simply exist or even live or reproduce. As Nussbaum 1 (2011) articulates: “Each creature has a characteristic set of capabilities, or capacities for functioning, distinctive of that species, and that those rudimentary capacities need support from the material and social environment if the animal is to flourish in it characteristic way.” (p.237). -
List of Marine Mammal Species & Subspecies
List of Marine Mammal Species & Subspecies The Committee on Taxonomy, chaired by Bill Perrin, produced the first official Society for Marine Mammalogy list of marine mammal species and subspecies in 2010 . Consensus on some issues was not possible; this is reflected in the footnotes. The list is updated annually. This version was updated in October 2015. This list can be cited as follows: “Committee on Taxonomy. 2015. List of marine mammal species and subspecies. Society for Marine Mammalogy, www.marinemammalscience.org, consulted on [date].” This list includes living and recently extinct (within historical times) species and subspecies, named and un-named. It is meant to reflect prevailing usage and recent revisions published in the peer-reviewed literature. An un-named subspecies is included if author(s) of a peer-reviewed article stated explicitly that the form is likely an undescribed subspecies. The Committee omits some described species and subspecies because of concern about their biological distinctness; reservations are given below. Author(s) and year of description of the species follow the Latin species name; when these are enclosed in parentheses, the species was originally described in a different genus. Classification and scientific names follow Rice (1998), with adjustments reflecting more recent literature. Common names are arbitrary and change with time and place; one or two currently frequently used names in English and/or a range language are given here. Additional English common names and common names in French, Spanish, Russian and other languages are available at www.marinespecies.org/cetacea/. Species and subspecies are listed in alphabetical order within families.