On Mesoplodon Carlhubbsi (Cetacea: Ziphiidae)
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Feeding Habits and Feeding Grounds of the Northern Elephant Seal Richard
FEEDING HABITS AND FEEDING GROUNDS OF THE NORTHERN ELEPHANT SEAL RICHARDCONDIT AND BUHNEYJ, LE BOEUF Department of Biology, University of California, Santa Cruz, CA 95064 ABSTRAC’r-Prey species consumed by northern elephant seals were identified from the stom- ach and throat contents of dead seals and from observations of prey captured. Their diet is catholic, consisting of a variety of pelagic, deep water squid, Pacific hake, sharks, rays, and ratfish. Feeding grounds of elephant seals were inferred from sightings of tagged elephant seals at non-rookery locations. Feeding areas extended from northern Baja California to northern Vancouver Island. Juveniles of both sexes and adult males moved north from their haul out sites in search of food, travelling furthest north during the summer. A few sightings suggested that adult females remain in the vicinity of the rookeries where they breed. Northern elephant seals, Mirounga angustirostris, breed and molt in large aggregations on land in Baja California and California, but spend the majority of the year feeding at sea. The large breeding aggregations are easy to observe and a great deal is known about the elephant seal’s reproductive behavior (Le Boeuf, 1974; Reiter et al., 1981). In contrast, the animals are rarely observed at sea and little is known about their feeding biology. Existing information on the food habits of the northern elephant seal comes from the exam- ination of stomach contents of only nine specimens (Huey, 1930; Freiberg and Dumas, 1954; Cowan and Guiguet, 1956; Morejohn and Baltz, 1970; Antonelis and Fiscus, 1980; Jones, 1981). The remains of sharks, ratfish, squids, and bony fish were identified. -
Early Stages of Fishes in the Western North Atlantic Ocean Volume
ISBN 0-9689167-4-x Early Stages of Fishes in the Western North Atlantic Ocean (Davis Strait, Southern Greenland and Flemish Cap to Cape Hatteras) Volume One Acipenseriformes through Syngnathiformes Michael P. Fahay ii Early Stages of Fishes in the Western North Atlantic Ocean iii Dedication This monograph is dedicated to those highly skilled larval fish illustrators whose talents and efforts have greatly facilitated the study of fish ontogeny. The works of many of those fine illustrators grace these pages. iv Early Stages of Fishes in the Western North Atlantic Ocean v Preface The contents of this monograph are a revision and update of an earlier atlas describing the eggs and larvae of western Atlantic marine fishes occurring between the Scotian Shelf and Cape Hatteras, North Carolina (Fahay, 1983). The three-fold increase in the total num- ber of species covered in the current compilation is the result of both a larger study area and a recent increase in published ontogenetic studies of fishes by many authors and students of the morphology of early stages of marine fishes. It is a tribute to the efforts of those authors that the ontogeny of greater than 70% of species known from the western North Atlantic Ocean is now well described. Michael Fahay 241 Sabino Road West Bath, Maine 04530 U.S.A. vi Acknowledgements I greatly appreciate the help provided by a number of very knowledgeable friends and colleagues dur- ing the preparation of this monograph. Jon Hare undertook a painstakingly critical review of the entire monograph, corrected omissions, inconsistencies, and errors of fact, and made suggestions which markedly improved its organization and presentation. -
Effects of Parasites on Marine Maniacs
EFFECTS OF PARASITES ON MARINE MANIACS JOSEPH R. GERACI and DAVID J. ST.AUBIN Department of Pathology Ontario Veterinary College University of Guefph Guelph, Ontario Canada INTRODUCTION Parasites of marine mammals have been the focus of numerous reports dealing with taxonomy, distribution and ecology (Defyamure, 1955). Descriptions of associated tissue damage are also available, with attempts to link severity of disease with morbidity and mortality of individuals and populations. This paper is not intended to duplicate that Iiterature. Instead we focus on those organisms which we perceive to be pathogenic, while tempering some of the more exaggerated int~~retations. We deal with life cycles by emphasizing unusual adap~t~ons of selected organisms, and have neces- sarily limited our selection of the literature to highlight that theme. For this discussion we address the parasites of cetaceans---baleen whales (mysticetes), and toothed whales, dolphins and porpoises (odon- tocetes): pinnipeds-true seals (phocidsf, fur seals and sea Iions (otariidsf and walruses (adobenids); sirenians~anatees and dugongs, and the djminutive sea otter. ECTOPARASITES We use the term “ectoparasite’” loosely, when referring to organisms ranging from algae to fish which somehow cling to the surface of a marine mammal, and whose mode of attachment, feeding behavior, and relationship with the host or transport animal are sufficiently obscure that the term parasite cannot be excluded. What is clear is that these organisms damage the integument in some way. For example: a whale entering the coid waters of the Antarctic can acquire a yelIow film over its body. Blue whales so discoiored are known as “sulfur bottoms”. -
Forage Fish Management Plan
Oregon Forage Fish Management Plan November 19, 2016 Oregon Department of Fish and Wildlife Marine Resources Program 2040 SE Marine Science Drive Newport, OR 97365 (541) 867-4741 http://www.dfw.state.or.us/MRP/ Oregon Department of Fish & Wildlife 1 Table of Contents Executive Summary ....................................................................................................................................... 4 Introduction .................................................................................................................................................. 6 Purpose and Need ..................................................................................................................................... 6 Federal action to protect Forage Fish (2016)............................................................................................ 7 The Oregon Marine Fisheries Management Plan Framework .................................................................. 7 Relationship to Other State Policies ......................................................................................................... 7 Public Process Developing this Plan .......................................................................................................... 8 How this Document is Organized .............................................................................................................. 8 A. Resource Analysis .................................................................................................................................... -
Defensive Behaviors of Deep-Sea Squids: Ink Release, Body Patterning, and Arm Autotomy
Defensive Behaviors of Deep-sea Squids: Ink Release, Body Patterning, and Arm Autotomy by Stephanie Lynn Bush A dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Integrative Biology in the Graduate Division of the University of California, Berkeley Committee in Charge: Professor Roy L. Caldwell, Chair Professor David R. Lindberg Professor George K. Roderick Dr. Bruce H. Robison Fall, 2009 Defensive Behaviors of Deep-sea Squids: Ink Release, Body Patterning, and Arm Autotomy © 2009 by Stephanie Lynn Bush ABSTRACT Defensive Behaviors of Deep-sea Squids: Ink Release, Body Patterning, and Arm Autotomy by Stephanie Lynn Bush Doctor of Philosophy in Integrative Biology University of California, Berkeley Professor Roy L. Caldwell, Chair The deep sea is the largest habitat on Earth and holds the majority of its’ animal biomass. Due to the limitations of observing, capturing and studying these diverse and numerous organisms, little is known about them. The majority of deep-sea species are known only from net-caught specimens, therefore behavioral ecology and functional morphology were assumed. The advent of human operated vehicles (HOVs) and remotely operated vehicles (ROVs) have allowed scientists to make one-of-a-kind observations and test hypotheses about deep-sea organismal biology. Cephalopods are large, soft-bodied molluscs whose defenses center on crypsis. Individuals can rapidly change coloration (for background matching, mimicry, and disruptive coloration), skin texture, body postures, locomotion, and release ink to avoid recognition as prey or escape when camouflage fails. Squids, octopuses, and cuttlefishes rely on these visual defenses in shallow-water environments, but deep-sea cephalopods were thought to perform only a limited number of these behaviors because of their extremely low light surroundings. -
Annotated Checklist of the Fish Species (Pisces) of La Réunion, Including a Red List of Threatened and Declining Species
Stuttgarter Beiträge zur Naturkunde A, Neue Serie 2: 1–168; Stuttgart, 30.IV.2009. 1 Annotated checklist of the fish species (Pisces) of La Réunion, including a Red List of threatened and declining species RONALD FR ICKE , THIE rr Y MULOCHAU , PA tr ICK DU R VILLE , PASCALE CHABANE T , Emm ANUEL TESSIE R & YVES LE T OU R NEU R Abstract An annotated checklist of the fish species of La Réunion (southwestern Indian Ocean) comprises a total of 984 species in 164 families (including 16 species which are not native). 65 species (plus 16 introduced) occur in fresh- water, with the Gobiidae as the largest freshwater fish family. 165 species (plus 16 introduced) live in transitional waters. In marine habitats, 965 species (plus two introduced) are found, with the Labridae, Serranidae and Gobiidae being the largest families; 56.7 % of these species live in shallow coral reefs, 33.7 % inside the fringing reef, 28.0 % in shallow rocky reefs, 16.8 % on sand bottoms, 14.0 % in deep reefs, 11.9 % on the reef flat, and 11.1 % in estuaries. 63 species are first records for Réunion. Zoogeographically, 65 % of the fish fauna have a widespread Indo-Pacific distribution, while only 2.6 % are Mascarene endemics, and 0.7 % Réunion endemics. The classification of the following species is changed in the present paper: Anguilla labiata (Peters, 1852) [pre- viously A. bengalensis labiata]; Microphis millepunctatus (Kaup, 1856) [previously M. brachyurus millepunctatus]; Epinephelus oceanicus (Lacepède, 1802) [previously E. fasciatus (non Forsskål in Niebuhr, 1775)]; Ostorhinchus fasciatus (White, 1790) [previously Apogon fasciatus]; Mulloidichthys auriflamma (Forsskål in Niebuhr, 1775) [previously Mulloidichthys vanicolensis (non Valenciennes in Cuvier & Valenciennes, 1831)]; Stegastes luteobrun- neus (Smith, 1960) [previously S. -
A Review of Direct and Indirect Impacts of Marine Dredging Activities on Marine Mammals
A review of direct and indirect impacts of marine dredging activities on marine mammals Family Scientific name Common name Range of best Frequency of Minimum Methodology Diet Region Habitat Documented Effects of Potential Effects of Dredging (excluding (including hearing (10 dB minimum hearing Dredging subspecies) subspecies) from max; kHz) hearing threshold (dB threshold (kHz) re 1 µPa) Otariidae Arctocephalus Cape & Unknown; — — — Fish (e.g. Emmelichthys nitidus, F, J (Kirkman et Continental shelf waters (IUCN, — Habitat destruction, increase in pusillus Australian fur fundamental Pseudophycis bachus, Trachurus al., 2007; IUCN, 2012) turbidity, changes to prey seal frequency of declivis, Neoplatycephalus 2013; Perrin, availability, masking, incidental male in air barks Richardsoni) (Australian fur seal) 2013) capture or injury, avoidance & is 0.14 & female (Page et al., 2005) an increase in shipping traffic in air barks is 0.15 (Tripovich et al., 2008) Arctophoca Antarctic fur seal Unknown; peak — — — Fish (e.g. Gymnoscopelus A, F, J (IUCN, Forage in deep waters (>500 m) — Habitat destruction, increase in gazella frequency of in piabilis, Electrona subaspera, 2013; Perrin, with a strong chlorophyll turbidity, changes to prey air barks is 0.3– Champsocephalus gunnari) 2013; Reeves et concentration & steep availability, masking, incidental 5.9 (Page et al., (Guinet et al., 2001) al., 2002) bathymetric gradients, otherwise capture or injury, avoidance & 2002) remains close to the colony in an increase in shipping traffic areas with Polar -
Bulletin 202
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Locomotor, Chromatic, Postural, and Bioluminescent Behaviors of the Deep-Sea Squid Octopoteuthis Deletron Young 1972
Reference: Biol. Bull. 216: 7–22. (February 2009) © 2009 Marine Biological Laboratory Behaving in the Dark: Locomotor, Chromatic, Postural, and Bioluminescent Behaviors of the Deep-Sea Squid Octopoteuthis deletron Young 1972 STEPHANIE L. BUSH1,2,*, BRUCE H. ROBISON2, AND ROY L. CALDWELL1 1University of California, Berkeley, Department of Integrative Biology, Berkeley, California 94720; and 2Monterey Bay Aquarium Research Institute, 7700 Sandholdt Rd., Moss Landing, California 95039 Abstract. Visual behaviors are prominent components of tion (Packard and Sanders, 1971; Packard and Hochberg, intra- and interspecific communication in shallow-water 1977; Hanlon and Messenger, 1988, 1996). These cephalo- cephalopods. Meso- and bathypelagic cephalopods were be- pods assess their surroundings with well-developed vision, lieved to have limited visual communication, other than biolu- though in most species vision is monochromatic (Messen- minescence, due to the reduced illumination at depth. To ger, 1977; Kito et al., 1992; Shashar et al., 1998; Sweeney explore potential visual behaviors in mesopelagic squid, we et al., 2007). Individuals are capable of polyphenism con- used undersea vehicles to observe 76 individuals of Octopo- sisting of near instantaneous changes in appearance through teuthis deletron. In contrast to predictions, we found this spe- a broad range of camouflage and communication methods cies capable of a variety of visually linked behaviors not (Packard and Sanders, 1971; Packard and Hochberg, 1977; previously reported for a deep-ocean cephalopod. The resultant Hanlon and Messenger, 1988; Roper and Hochberg, 1988; ethogram describes numerous chromatic, postural, locomotor, Hanlon et al., 1999a; Barbato et al., 2007). An individual’s and bioluminescent behavioral components. A few common overall appearance, or body pattern, is composed of the body patterns—the whole appearance of the individual involv- following component types: chromatic, textural, postural, ing multiple components—are characterized. -
Visual Cognition in Deep-Sea Cephalopods: What We Don't
Trim: 247mm × 174mm Top: 12.653mm Gutter: 16.871mm CUUK2624-10 CUUK2624/Darmaillacq ISBN: 978 1 107 01556 2 March 13, 2014 11:45 10 Visual cognition in deep-sea cephalopods: what we don’t know and why we don’t know it Sarah Zylinski and Sonke¨ Johnsen 10.1 The other cephalopods A quick glance at the recent cephalopod literature, or even at the chapters of this book, tells us that when we talk about cephalopod cognition we are really considering cognition in a handful of genera. There can be no argument that studies of these animals have led to remarkable results that have challenged the traditional view of invertebrate intelligence. Yet when we consider that less than 10 species of cephalopod are commonly seen as the focus of behavioral studies, let alone in studies specifically about cognition, it becomes apparent that claims regarding the cognitive capabilities of cephalopods are generali- zations drawn from work on a handful of genera. The majority of the 800 or so described species of cephalopod do not share the neritic and near-shore benthic habitats of the taxa with which we are most familiar; virtually unknown in terms of their behaviour and ecology, these species inhabit a different world in the deep, dark waters of the open ocean (Figure 10.1). In this chapter, we introduce and discuss the neglected cephalopods of the deep sea, many of which are not so distantly related to the species with which we are familiar, but whose existence in the deep sea has little in common with the complex reefs and near- shore habitats associated with taxa such as Octopus and Sepia. -
Ken Schultz's Field Guide to Saltwater Fish
ffirs.qxd 10/31/03 9:25 AM Page iii • • • • KEN SCHULTZ’S Field Guide to Saltwater Fish by Ken Schultz JOHN WILEY & SONS, INC. ffirs.qxd 10/31/03 9:25 AM Page i • • • • KEN SCHULTZ’S Field Guide to Saltwater Fish ffirs.qxd 10/31/03 9:25 AM Page ii ffirs.qxd 10/31/03 9:25 AM Page iii • • • • KEN SCHULTZ’S Field Guide to Saltwater Fish by Ken Schultz JOHN WILEY & SONS, INC. ffirs.qxd 10/31/03 9:25 AM Page iv This book is printed on acid-free paper. Copyright © 2004 by Ken Schultz. All rights reserved Published by John WIley & Sons, Inc., Hoboken, New Jersey Published simultaneously in Canada Design and production by Navta Associates, Inc. No part of this publication may be reproduced, stored in a retrieval system, or trans- mitted in any form or by any means, electronic, mechanical, photocopying, recording, scanning, or otherwise, except as permitted under Section 107 or 108 of the 1976 United States Copyright Act, without either the prior written permission of the Pub- lisher, or authorization through payment of the appropriate per-copy fee to the Copy- right Clearance Center, 222 Rosewood Drive, Danvers, MA 01923, (978) 750-8400, fax (978) 750-4470, or on the web at www.copyright.com. Requests to the Publisher for permission should be addressed to the Permissions Department, John Wiley & Sons, Inc., 111 River Street, Hoboken, NJ 07030, (201) 748-6011, fax (201) 748-6008, email: [email protected]. Limit of Liability/Disclaimer of Warranty: While the publisher and the author have used their best efforts in preparing this book, they make no representations or warranties with respect to the accuracy or completeness of the contents of this book and specifi- cally disclaim any implied warranties of merchantability or fitness for a particular purpose. -
Curriculum Vitae Bruce H. Robison
Curriculum Vitae Bruce H. Robison Present Position Senior Scientist, Monterey Bay Aquarium Research Institute, 1987 – MBARI Science Department Chair, 1991 - 1996 MBARI Research Division Chair, 2012 – 2016 Education B.S., Biological Sciences, Purdue University, 1965 M.A., Marine Science, College of William & Mary: VIMS, 1968 Ph.D., Biological Oceanography, Stanford University, HMS, 1973 Certification: Scientific Research Pilot for ADS submersibles, 1982; 2000 Previous Positions Woods Hole Oceanographic Institution, Woods Hole, MA Postdoctoral Fellow, 1973. Postdoctoral Investigator, 1974. Marine Science Institute, University of California, Santa Barbara Assistant Research Oceanographer 1974 - 1982 Associate Research Oceanographer 1982 - 1988. Honors/Awards Fellow, California Academy of Sciences, 1991 Antarctic Service Medal, 1992 Morris Scholar in Residence - University of Maryland, Horn Point, 1996 Monterey Bay National Marine Sanctuary, Science/Research Award, 1997 Fellow, American Association for the Advancement of Science, 1998 Marine Technology Society; Lockheed Martin Award for Ocean Science and Engineering, 2002 Chautauqua Institution of New York, Carnahan-Jackson Lecturer, 2003 University Distinguished Lecturer; Texas A&M University, 2006 Steinbach Visiting Scholar; Joint Program, Massachusetts Institute of Technology/Woods Hole Oceanographic Institution, 2006 Resident Scholar; Rockefeller Foundation, Bellagio Center, Italy, for research on the Conservation of Deep Pelagic Biodiversity, 2007 Ed Ricketts Memorial Award for Lifetime