Scientific Classification
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												  Fig. 125 Sharks of the World, Vol. 2 161 Fig. 125 Orectolobus Sp. Aclick for previous page Sharks of the World, Vol. 2 161 Orectolobus sp. A Last and Stevens, 1994 Fig. 125 Orectolobus sp. A Last and Stevens, 1994, Sharks Rays Australia: 128, pl. 26. Synonyms: None. Other Combinations: None. FAO Names: En - Western wobbegong; Fr - Requin-tapis sombre; Sp - Tapicero occidental. LATERAL VIEW DORSAL VIEW Fig. 125 Orectolobus sp. A UNDERSIDE OF HEAD Field Marks: Flattened benthic sharks with dermal lobes on sides of head, symphysial groove on chin; a strongly contrasting, variegated colour pattern of conspicuous broad dark, dorsal saddles with light spots and deeply corrugated edges but without conspicuous black margins, interspaced with lighter areas and conspicuous light, dark-centred spots but without numerous light O-shaped rings; also, mouth in front of eyes, long, basally branched nasal barbels, nasoral grooves and circumnarial grooves, two rows of enlarged fang-like teeth in upper jaw and three in lower jaw; first dorsal-fin origin over rear half of pelvic-fin bases. Diagnostic Features: Nasal barbels with one small branch. Four dermal lobes below and in front of eye on each side of head; dermal lobes behind spiracles unbranched or weakly branched and slender. Low dermal tubercles or ridges present on back in young, lost in adults. Interdorsal space somewhat shorter than inner margin of first dorsal fin, about one-fourth of first dorsal-fin base. Origin of first dorsal fin over about last third of pelvic-fin base. First dorsal-fin height about three-fourths of base length. Colour: colour pattern very conspicuous and highly variegated, dorsal surface of body with conspicuous broad, dark rectangular saddles with deeply corrugated margins, not black-edged, dotted with light spots but without numerous O-shaped light rings; saddles not ocellate in appearance; interspaces between saddles light, with numerous broad dark blotches.
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												  © Iccat, 2007A5 By-catch Species APPENDIX 5: BY-CATCH SPECIES A.5 By-catch species By-catch is the unintentional/incidental capture of non-target species during fishing operations. Different types of fisheries have different types and levels of by-catch, depending on the gear used, the time, area and depth fished, etc. Article IV of the Convention states: "the Commission shall be responsible for the study of the population of tuna and tuna-like fishes (the Scombriformes with the exception of Trichiuridae and Gempylidae and the genus Scomber) and such other species of fishes exploited in tuna fishing in the Convention area as are not under investigation by another international fishery organization". The following is a list of by-catch species recorded as being ever caught by any major tuna fishery in the Atlantic/Mediterranean. Note that the lists are qualitative and are not indicative of quantity or mortality. Thus, the presence of a species in the lists does not imply that it is caught in significant quantities, or that individuals that are caught necessarily die. Skates and rays Scientific names Common name Code LL GILL PS BB HARP TRAP OTHER Dasyatis centroura Roughtail stingray RDC X Dasyatis violacea Pelagic stingray PLS X X X X Manta birostris Manta ray RMB X X X Mobula hypostoma RMH X Mobula lucasana X Mobula mobular Devil ray RMM X X X X X Myliobatis aquila Common eagle ray MYL X X Pteuromylaeus bovinus Bull ray MPO X X Raja fullonica Shagreen ray RJF X Raja straeleni Spotted skate RFL X Rhinoptera spp Cownose ray X Torpedo nobiliana Torpedo
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												  Florida's Fintastic Sharks and Rays Lesson and Activity PacketFlorida's Fintastic Sharks and Rays An at-home lesson for grades 3-5 Produced by: This educational workbook was produced through the support of the Indian River Lagoon National Estuary Program. 1 What are sharks and rays? Believe it or not, they’re a type of fish! When you think “fish,” you probably picture a trout or tuna, but fishes come in all shapes and sizes. All fishes share the following key characteristics that classify them into this group: Fishes have the simplest of vertebrate hearts with only two chambers- one atrium and one ventricle. The spine in a fish runs down the middle of its back just like ours, making fish vertebrates. All fishes have skeletons, but not all fish skeletons are made out of bones. Some fishes have skeletons made out of cartilage, just like your nose and ears. Fishes are cold-blooded. Cold-blooded animals use their environment to warm up or cool down. Fins help fish swim. Fins come in pairs, like pectoral and pelvic fins or are singular, like caudal or anal fins. Later in this packet, we will look at the different types of fins that fishes have and some of the unique ways they are used. 2 Placoid Ctenoid Ganoid Cycloid Hard protective scales cover the skin of many fish species. Scales can act as “fingerprints” to help identify some fish species. There are several different scale types found in bony fishes, including cycloid (round), ganoid (rectangular or diamond), and ctenoid (scalloped). Cartilaginous fishes have dermal denticles (Placoid) that resemble tiny teeth on their skin.
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												  Evolutionary Relations of Hexanchiformes Deep-Sea Sharks Elucidated by Whole Mitochondrial Genome SequencesHindawi Publishing Corporation BioMed Research International Volume 2013, Article ID 147064, 11 pages http://dx.doi.org/10.1155/2013/147064 Research Article Evolutionary Relations of Hexanchiformes Deep-Sea Sharks Elucidated by Whole Mitochondrial Genome Sequences Keiko Tanaka,1 Takashi Shiina,1 Taketeru Tomita,2 Shingo Suzuki,1 Kazuyoshi Hosomichi,3 Kazumi Sano,4 Hiroyuki Doi,5 Azumi Kono,1 Tomoyoshi Komiyama,6 Hidetoshi Inoko,1 Jerzy K. Kulski,1,7 and Sho Tanaka8 1 Department of Molecular Life Science, Division of Basic Medical Science and Molecular Medicine, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 259-1143, Japan 2 Fisheries Science Center, The Hokkaido University Museum, 3-1-1 Minato-cho, Hakodate, Hokkaido 041-8611, Japan 3 Division of Human Genetics, Department of Integrated Genetics, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka 411-8540, Japan 4 Division of Science Interpreter Training, Komaba Organization for Education Excellence College of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo 153-8902, Japan 5 Shimonoseki Marine Science Museum, 6-1 Arcaport, Shimonoseki, Yamaguchi 750-0036, Japan 6 Department of Clinical Pharmacology, Division of Basic Clinical Science and Public Health, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 259-1143, Japan 7 Centre for Forensic Science, The University of Western Australia, Nedlands, WA 6008, Australia 8 Department of Marine Biology, School of Marine Science and Technology, Tokai University, 3-20-1 Orido, Shimizu, Shizuoka 424-8610, Japan Correspondence should be addressed to Takashi Shiina; [email protected] Received 1 March 2013; Accepted 26 July 2013 Academic Editor: Dietmar Quandt Copyright © 2013 Keiko Tanaka et al.
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												  Identification Guide to the Deep-Sea Cartilaginous Fishes OfIdentification guide to the deep–sea cartilaginous fishes of the Southeastern Atlantic Ocean FAO. 2015. Identification guide to the deep–sea cartilaginous fishes of the Southeastern Atlantic Ocean. FishFinder Programme, by Ebert, D.A. and Mostarda, E., Rome, Italy. Supervision: Merete Tandstad, Jessica Sanders (FAO, Rome) Technical editor: Edoardo Mostarda (FAO, Rome) Colour illustrations, cover and graphic design: Emanuela D’Antoni (FAO, Rome) This guide was prepared under the “FAO Deep–sea Fisheries Programme” thanks to a generous funding from the Government of Norway (Support to the implementation of the International Guidelines on the Management of Deep-Sea Fisheries in the High Seas project) for the purpose of assisting states, institutions, the fishing industry and RFMO/As in the implementation of FAO International Guidelines for the Management of Deep-sea Fisheries in the High Seas. It was developed in close collaboration with the FishFinder Programme of the Marine and Inland Fisheries Branch, Fisheries Department, Food and Agriculture Organization of the United Nations (FAO). The present guide covers the deep–sea Southeastern Atlantic Ocean and that portion of Southwestern Indian Ocean from 18°42’E to 30°00’E (FAO Fishing Area 47). It includes a selection of cartilaginous fish species of major, moderate and minor importance to fisheries as well as those of doubtful or potential use to fisheries. It also covers those little known species that may be of research, educational, and ecological importance. In this region, the deep–sea chondrichthyan fauna is currently represented by 50 shark, 20 batoid and 8 chimaera species. This guide includes full species accounts for 37 shark, 9 batoid and 4 chimaera species selected as being the more difficult to identify and/or commonly caught.
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												  Interspecific and Intraspecific Variability in Placoid Scale Morphology in Relation to Body Form Variability in SqualiformesW&M ScholarWorks Dissertations, Theses, and Masters Projects Theses, Dissertations, & Master Projects 1993 Interspecific and intraspecific ariabilityv in placoid scale morphology in relation to body form variability in squaliformes Christopher R. Tabit College of William and Mary - Virginia Institute of Marine Science Follow this and additional works at: https://scholarworks.wm.edu/etd Part of the Fresh Water Studies Commons, Marine Biology Commons, Ocean Engineering Commons, and the Oceanography Commons Recommended Citation Tabit, Christopher R., "Interspecific and intraspecific ariabilityv in placoid scale morphology in relation to body form variability in squaliformes" (1993). Dissertations, Theses, and Masters Projects. Paper 1539616872. https://dx.doi.org/doi:10.25773/v5-3hhf-db24 This Dissertation is brought to you for free and open access by the Theses, Dissertations, & Master Projects at W&M ScholarWorks. It has been accepted for inclusion in Dissertations, Theses, and Masters Projects by an authorized administrator of W&M ScholarWorks. For more information, please contact [email protected]. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted.
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												  Xenacanthus (Chondrichthyes: Xenacanthiformes) from North AmericaActa Geologica Polonica, Vol. 49 (J 999), No.3, pp. 215-266 406 IU S UNES 0 I Dentitions of Late Palaeozoic Orthacanthus species and new species of ?Xenacanthus (Chondrichthyes: Xenacanthiformes) from North America GARY D. JOHNSON Department of Earth Sciences and Physics, University of South Dakota; 414 East Clark Street, Vermillion, SD 57069-2390, USA. E-mail: [email protected] ABSTRACT: JOHNSON, G.D. 1999. Dentitions of Late Palaeozoic Orthacanthus species and new species of ?Xenacanthus (Chondrichthyes: Xenacanthiformes) from North America. Acta Geologica Polonica, 49 (3),215-266. Warszawa. Orthacanthus lateral teeth have paired, variably divergent, smooth, usually carinated labio-lingually compressed principal cusps separated by a central foramen; one or more intermediate cusps; and an api cal button on the base isolated from the cusps. Several thousand isolated teeth from Texas Artinskian bulk samples are used to define the heterodont dentitions of O. texensis and O. platypternus. The O. tex ensis tooth base has a labio-Iingual width greater than the anteromedial-posterolateral length, the basal tubercle is restricted to the thick labial margin, the principal cusps are serrated to varying degrees, and the posterior cusp is larger. The O. platypternus tooth base is longer than wide, its basal tubercle extends to the center, the labial margin is thin, serrations are absent on the principal cusps, the anterior cusp is larger, and a single intermediate cusp is present. More than two hundred isolated teeth from Nebraska (Gzhelian) and Pennsylvania (Asselian) provide a preliminary description of the heterodont dentition of O. compress us . The principal cusps are similar to O.
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												  Integrating Multiple Chemical Tracers to Elucidate the Diet and Habitat of Cookiecutter Sharks Aaron Bwww.nature.com/scientificreports OPEN Integrating multiple chemical tracers to elucidate the diet and habitat of Cookiecutter Sharks Aaron B. Carlisle1*, Elizabeth Andruszkiewicz Allan2,9, Sora L. Kim3, Lauren Meyer4,5, Jesse Port6, Stephen Scherrer7 & John O’Sullivan8 The Cookiecutter shark (Isistius brasiliensis) is an ectoparasitic, mesopelagic shark that is known for removing plugs of tissue from larger prey, including teleosts, chondrichthyans, cephalopods, and marine mammals. Although this species is widely distributed throughout the world’s tropical and subtropical oceanic waters, like many deep-water species, it remains very poorly understood due to its mesopelagic distribution. We used a suite of biochemical tracers, including stable isotope analysis (SIA), fatty acid analysis (FAA), and environmental DNA (eDNA), to investigate the trophic ecology of this species in the Central Pacifc around Hawaii. We found that large epipelagic prey constituted a relatively minor part of the overall diet. Surprisingly, small micronektonic and forage species (meso- and epipelagic) are the most important prey group for Cookiecutter sharks across the studied size range (17–43 cm total length), with larger mesopelagic species or species that exhibit diel vertical migration also being important prey. These results were consistent across all the tracer techniques employed. Our results indicate that Cookiecutter sharks play a unique role in pelagic food webs, feeding on prey ranging from the largest apex predators to small, low trophic level species, in particular those that overlap with the depth distribution of the sharks throughout the diel cycle. We also found evidence of a potential shift in diet and/or habitat with size and season.
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												  Petrified Forest U.SNational Park Service Petrified Forest U.S. Department of the Interior Petrified Forest National Park Petrified Forest, Arizona Triassic Dinosaurs and Other Animals Fossils are clues to the past, allowing researchers to reconstruct ancient environments. During the Late Triassic, the climate was very different from that of today. Located near the equator, this region was humid and tropical, the landscape dominated by a huge river system. Giant reptiles and amphibians, early dinosaurs, fish, and many invertebrates lived among the dense vegetation and in the winding waterways. New fossils come to light as paleontologists continue to study the Triassic treasure trove of Petrified Forest National Park. Invertebrates Scattered throughout the sedimentary species forming vast colonies in the layers of the Chinle Formation are fossils muddy beds of the ancient lakes and of many types of invertebrates. Trace rivers. Antediplodon thomasi is one of the fossils include insect nests, termite clam fossils found in the park. galleries, and beetle borings in the petrified logs. Thin slabs of shale have preserved Horseshoe crabs more delicate animals such as shrimp, Horseshoe crabs have been identified by crayfish, and insects, including the wing of their fossilized tracks (Kouphichnium a cockroach! arizonae), originally left in the soft sediments at the bottom of fresh water Clams lakes and streams. These invertebrates Various freshwater bivalves have been probably ate worms, soft mollusks, plants, found in the Chinle Formation, some and dead fish. Freshwater Fish The freshwater streams and rivers of the (pictured). This large lobe-finned fish Triassic landscape were home to numerous could reach up to 5 feet (1.5 m) long and species of fish.
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												  New Evidence of Predation on Humans by Cookiecutter Sharks in Kauai, HawaiiInternational Journal of Legal Medicine https://doi.org/10.1007/s00414-018-1786-8 CASE REPORT New evidence of predation on humans by cookiecutter sharks in Kauai, Hawaii Agathe Ribéreau-Gayon1,2,3 & David O. Carter4 & Stephanie Regan5 Received: 7 December 2017 /Accepted: 17 January 2018 # The Author(s) 2018. This article is an open access publication Abstract The feeding patterns of species of large sharks on human corpses are well documented in the literature however, that of smaller sharks are less known. This may introduce uncertainty in the medicolegal conclusions. For that reason, accurate identification of patterns of shark predation is very relevant, specifically in areas bordered by the sea. In the case described here, an unidentified lesion was noted on the body of a victim of a scuba diving accident off the island of Kauai, in Hawaii. The aim of this study was to identify the origin of the lesion and investigate its potential to inform on the context of death and/or decomposition. The original outline of the lesion was digitally reconstructed to enable the collection of measurements which were compared with the literature and interpreted with an interdisciplinary approach. This approach permitted to determine that the macroscopic appearance and dimensions of the lesion (major axis = 3.53 cm) were consistent with a bitemark of a cookiecutter shark (Isistius brasiliensis). It was further determined that the bitemark was incomplete and that the specimen involved had a total length of about 24 cm and was likely to be a juvenile. This is the second report in the published literature of cookiecutter bitemarks on humans in the Hawaiian waters.
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												  Biomechanics of Locomotion in Sharks, Rays, and Chimaeras5 Biomechanics of Locomotion in Sharks, Rays, and Chimaeras Anabela M.R. Maia, Cheryl A.D. Wilga, and George V. Lauder CONTENTS 5.1 Introduction 125 5.1.1 Approaches to Studying Locomotion in Chondrichthyans 125 5.1.2 Diversity of Locomotory Modes in Chondrichthyans 127 5.1.3 Body Form and Fin Shapes 127 5.2 Locomotion in Sharks 128 5.2.1 Function of the Body during Steady Locomotion and Vertical Maneuvering 128 5.2.2 Function of the Caudal Fin during Steady Locomotion and Vertical Maneuvering 130 5.2.3 Function of the Pectoral Fins during Locomotion 134 5.2.3.1 Anatomy of the Pectoral Fins 134 5.2.3.2 Role of the Pectoral Fins during Steady Swimming 136 5.2.3.3 Role of the Pectoral Fins during Vertical Maneuvering 138 5.2.3.4 Function of the Pectoral Fins during Benthic Station-Holding 139 5.2.3.5 Motor Activity in the Pectoral Fins 139 5.2.4 Routine Maneuvers and Escape Responses 140 5.2.5 Synthesis 141 5.3 Locomotion in Skates and Rays 142 5.4 Locomotion in Holocephalans 145 5.5 Material Properties of Chondrichthyan Locomotor Structures 146 5.6 Future Directions 147 Acknowledgments 148 References 148 5.1.1 Approaches to Studying 5.1 Introduction Locomotion in Chondrichthyans The body form of sharks is notable for the distinctive Historically, many attempts have been made to under- heterocercal tail with external morphological asymme- stand the function of the median and paired fins in try present in most taxa and the ventrolateral winglike sharks and rays, and these studies have included work pectoral fins extending laterally from the body (Figure with models (Affleck.
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												  NEA Shark CoversThis report describes the results of a regional Red List Workshop held at the Joint Nature Conservation Committee (JNCC), Peterborough, UK, in 2006, as a contribution towards the IUCN Species Survival Commission’s Shark Specialist Group’s ‘Global Shark Red List Assessment’. The purpose of the workshop was to assess the conservation status of the chondrichthyan fishes (sharks, rays and chimaeras) of the Northeast Atlantic region (FAO Major Fishery Area 27). This region is bordered by some of the largest and most important chondrichthyan fishing nations in the world, including Spain, France, the UK and Portugal. A regional overview of fisheries, utilisation, trade, management and conservation is also presented. The Northeast Atlantic chondrichthyan fauna is moderately diverse, with an estimated 118 species (approximately 11% of total living chondrichthyans). These occur within a huge range of habitats, including the deep-sea, open oceans, and coastal waters from the Arctic to the Mediterranean. During the workshop, experts collated information and prepared 74 global and 17 regional species assessments, thereby completing the Red Listing process for the described chondrichthyan fauna of the Northeast Atlantic (two undescribed species were not assessed). These assessments were agreed by consensus throughout the SSG network prior to their submission to IUCN Red List of Threatened SpeciesTM. Results show that 26% of Northeast Atlantic chondrichthyans are threatened within the region (7% Critically Endangered, 7% Endangered, 12% Vulnerable). A further 20% are Near Threatened, 27% Least Concern and 27% are Data Deficient. This is a significantly higher level of threat than that for the whole taxonomic group, worldwide. Globally, of the 1, 038 species of chondrichthyans assessed, 18% are threatened (3% CR, 4% EN, 11% VU), 13% are Near Threatened, 23% Least Concern and 46% Data Deficient.