Assessing Shark and Ray Bycatch in Indonesian

Total Page:16

File Type:pdf, Size:1020Kb

Assessing Shark and Ray Bycatch in Indonesian ASSESSING SHARK AND RAY BYCATCH IN INDONESIAN DEEPWATER SNAPPER-GROUPER FISHERIES FINAL REPORT Prepared for The Nature Conservancy Indonesia by Vanessa Jaiteh, Coral Reef Research Foundation February 2017 ASSESSING SHARK BYCATCH IN INDONESIAN DEEP-­‐SLOPE SNAPPER-­‐GROUPER FISHERIES TABLE OF CONTENTS 1. Background and Objectives .................................................................................... 3 2. CODRS Image Analysis ........................................................................................... 3 Summary .................................................................................................................. 3 Species composition ................................................................................................ 5 Geographic distribution of shark bycatch .............................................................. 11 Occurrence of recent pups and juvenile sharks ..................................................... 15 3. Species of Concern ............................................................................................... 15 4. Recommendations for monitoring shark bycatch ................................................. 16 Consistent recording of shark and ray bycatch ...................................................... 16 Image composition ................................................................................................ 18 5. Conclusions ........................................................................................................... 20 2 ASSESSING SHARK BYCATCH IN INDONESIAN DEEP-­‐SLOPE SNAPPER-­‐GROUPER FISHERIES 1. BACKGROUND AND OBJECTIVES Fisheries certification schemes, such as the Marine Stewardship Council (MSC), are gaining popularity as a means of promoting seafood sustainability and food security, and meeting an increasing global demand for sustainably sourced seafood. As one of the world’s leading seafood producers, Indonesia has struggled to achieve seafood certification in many of its fisheries, but recent national developments have sparked increased efforts to this end. Shark and ray (hereafter referred to as ‘shark’) bycatch is a particular challenge to MSC and other certification schemes due to the relatively recent, but in some cases severe, declines in a number of shark populations as a result of their capture in target fisheries and as bycatch. Since 2014, The Nature Conservancy (TNC) is working towards MSC certification with a number of Indonesian deep-slope (50-500m) dropline and demersal longline fisheries that target various snapper, grouper and emperor species. With homeports and fishing grounds in many parts of central and eastern Indonesia, the catch of sharks is likely to vary by species, geographic region, fishing gear, and depth. Shark bycatch and its mitigation is an essential consideration in the MSC certification process. The purpose of this work was therefore to identify the shark and ray species caught in Indonesian deep- slope fisheries and to provide advice on how to routinely monitor shark bycatch. This was achieved using images of the catch recorded by captains onboard fishing vessels as part of the Captain Operated Data Recording System (CODRS). Images in the CODRS were also used to develop a species check list and species identification aids, as well as an illustrated instruction sheet for captains on best practices in taking photos to aid species identification. 2. CODRS IMAGE ANALYSIS SUMMARY Twenty-seven vessels submitted a total of 153 photographs of sharks and rays to CODRS. Photographs were taken on 81 days between 17th October 2015 and 29th 3 ASSESSING SHARK BYCATCH IN INDONESIAN DEEP-­‐SLOPE SNAPPER-­‐GROUPER FISHERIES October 2016. From 248 individuals that were recognized on these images, 12 were cobias (i.e. shark look-alike teleost fish), and at least 29 individuals, possibly more, were photographed more than once. Although this means that a definite total count of individuals is not possible, an estimated 207 were distinct individuals that belonged to at least 36 species and 18 families (see species list in Table 1 below). Table 1. List of shark and ray species recorded from CODRS images Family Genus Species Common name Carcharhinidae Carcharhinus albimarginatus Silvertip shark Carcharhinidae Carcharhinus altimus Bignose shark Carcharhinidae Carcharhinus amblyrhynchoides Graceful shark Carcharhinidae Carcharhinus amblyrhynchos Grey reef shark Carcharhinidae Carcharhinus amboinensis Pigeye shark Carcharhinidae Carcharhinus falciformis Silky shark Carcharhinidae Carcharhinus limbatus Blacktip shark Carcharhinidae Carcharhinus obscurus Dusky whaler Carcharhinidae Carcharhinus plumbeus Sandbar shark Carcharhinidae Carcharhinus sorrah Spot-tail shark Carcharhinidae Galeocerdo cuvier Tiger shark Carcharhinidae Loxodon macrorhinus Sliteye shark Carcharhinidae Negaprion acutidens Lemon shark Carcharhinidae Rhizoprionodon acutus Milk shark Carcharhinidae Rhizoprionodon oligolinx Grey sharpnose shark Carcharhinidae Triaenodon obesus Whitetip reef shark Carcharhinidae Carcharhinus sp. Whaler shark Centrophoridae Centrophorus sp. Gulper shark Dasyatidae Himantura uarnak Reticulate whipray Ginglymostomatidae Nebrius ferrugineus Tawny nurse shark Hemigaleidae Hemipristis elongata Fossil shark Hemiscyllidae Chiloscyllium punctatum Brownbanded bambooshark Hexanchidae Hexanchus nakamurai Bigeye sixgill shark Lamnidae Isurus oxyrinchus Shortfin mako Myliobatidae Aetobatus narinari Spotted eagle ray Orectolobidae Orectolobus ornatus Indo wobbegong Orectolobidae Orectolobus sp. Wobbegong shark Rhincodontidae Rhincodon typus Whale shark (not captured) 4 ASSESSING SHARK BYCATCH IN INDONESIAN DEEP-­‐SLOPE SNAPPER-­‐GROUPER FISHERIES Family Genus Species Common name Rhinidae Rhina ancylostoma Shark ray Rhinobatidae Rhinobatos sp. Shovelnose ray Rhynchobatidae Rhynchobatus australiae Whitespotted guitafish Rhynchobatidae Rhynchobatus laevis Smoothnose wedgefish Sphyrnidae Sphyrna lewini Scalloped hammerhead Sphyrnidae Sphyrna mokarran Great hammerhead Squalidae Squalus sp. Spurdog shark Stegostomatidae Stegostoma fasciatum Leopard shark Triakidae Hemitriakis sp. Houndshark SPECIES COMPOSITION The shark bycatch was dominated by Carcharhinids, also known as requiem or whaler sharks, which made up 56% of the catch (n= 110, Figure 1). A further 11% and 9% of the catch was made up of hammerhead sharks (Sphyrnidae, n= 22), mainly of the species Sphyrna lewini (scalloped hammerhead) and guitarfish (family Rhynchobatidae, n= 17), most of which were whitespotted guitarfish, Rhynchobatos australiae. The remaining 15 families contributed 5% or less to the total catch (Figure 1). Finally, 12 individuals mistakenly assigned to the CODRS shark images database were cobia (Rachycentron canadum, family Rachycentridae). Although shark look- alikes, they are teleost fish with rays in their fins. 5 ASSESSING SHARK BYCATCH IN INDONESIAN DEEP-­‐SLOPE SNAPPER-­‐GROUPER FISHERIES Carcharhinidae Sphyrnidae Rhynchobatidae Centrophoridae Rhinidae Hemiscyllidae Triakidae Squalidae Orectolobidae Lamnidae Family Stegostomatidae Rhinobatidae Hexanchidae Dasyatidae Rhincodontidae Myliobatidae Hemigaleidae Ginglymostomatidae 0% 10% 20% 30% 40% 50% 60% Percentage in catch Figure 1. Proportion of individuals from each identified taxonomic family that made up the shark and ray bycatch recorded in the central and eastern Indonesian deep- slope snapper and grouper fishery. In terms of individual species, the spot-tail shark Carcharhinus sorrah was the most abundant (n = 28), followed by the scalloped hammerhead shark Sphyrna lewini (n = 21, Figure 2). Tiger sharks, whitespotted guitarfish, silvertips and gulper sharks were all represented by at least 10 individuals. Other, less abundant species included two reticulate whiprays (Himantura uarnak), an eagle ray (Aetobatus narinari), a tawny nurse shark (Nebrius ferrugineus), two wobbegong sharks (Orectolobus sp.) and a fossil shark (Hemipristis elongata, Figure 2). The latter was only recently described as occurring in eastern Indonesia; previously its range was thought to extend only to the eastern coast of Java. This CODRS record of a fossil shark provides further evidence of the presence of this species in central and eastern Indonesia, and highlights the usefulness of fisher-contributed data to the advancement of scientific knowledge. 6 ASSESSING SHARK BYCATCH IN INDONESIAN DEEP-­‐SLOPE SNAPPER-­‐GROUPER FISHERIES Carcharhinus sorrah Sphyrna lewini Galeocerdo cuvier Unidentified Rhynchobatus australie Carcharhinus albimarginatus Centrophorus sp. Carcharhinus amblyrhynchos Carcharhinus amboinensis Carcharhinus sp. Rhizoprionodon acutus Rhina ancylostoma Chiloscyllium punctatum Rhynchobatus laevis Loxodon macrorhinus Carcharhinus limbatus Squalus sp. Rhizoprionodon acutus Hemitriakis sp. Carcharhinus plumbeus Stegostoma fasciatum Species Orectolobus cf ornatus Negaprion acutidens Hexanchus nakamurai Carcharhinus obscurus Himantura uarnak Isurus oxyrinchus Triaenodon obesus Sphyrna mokarran Rhizoprionodon oligolinx Rhinobatos sp. Rhincodon typus Orectolobus sp. Nebrius ferrugineus Hemipristis elongata Carcharhinus melanopterus Carcharhinus falciformis Carcharhinus amblyrhynchoides Carcharhinus altimus Aetobatus narinari 0 5 10 15 20 25 30 Number of individuals Figure 2. The number of individuals of each species recorded from CODRS images 7 ASSESSING SHARK BYCATCH IN INDONESIAN DEEP-­‐SLOPE SNAPPER-­‐GROUPER FISHERIES Several individuals could only be identified to genus level and
Recommended publications
  • An Introduction to the Classification of Elasmobranchs
    An introduction to the classification of elasmobranchs 17 Rekha J. Nair and P.U Zacharia Central Marine Fisheries Research Institute, Kochi-682 018 Introduction eyed, stomachless, deep-sea creatures that possess an upper jaw which is fused to its cranium (unlike in sharks). The term Elasmobranchs or chondrichthyans refers to the The great majority of the commercially important species of group of marine organisms with a skeleton made of cartilage. chondrichthyans are elasmobranchs. The latter are named They include sharks, skates, rays and chimaeras. These for their plated gills which communicate to the exterior by organisms are characterised by and differ from their sister 5–7 openings. In total, there are about 869+ extant species group of bony fishes in the characteristics like cartilaginous of elasmobranchs, with about 400+ of those being sharks skeleton, absence of swim bladders and presence of five and the rest skates and rays. Taxonomy is also perhaps to seven pairs of naked gill slits that are not covered by an infamously known for its constant, yet essential, revisions operculum. The chondrichthyans which are placed in Class of the relationships and identity of different organisms. Elasmobranchii are grouped into two main subdivisions Classification of elasmobranchs certainly does not evade this Holocephalii (Chimaeras or ratfishes and elephant fishes) process, and species are sometimes lumped in with other with three families and approximately 37 species inhabiting species, or renamed, or assigned to different families and deep cool waters; and the Elasmobranchii, which is a large, other taxonomic groupings. It is certain, however, that such diverse group (sharks, skates and rays) with representatives revisions will clarify our view of the taxonomy and phylogeny in all types of environments, from fresh waters to the bottom (evolutionary relationships) of elasmobranchs, leading to a of marine trenches and from polar regions to warm tropical better understanding of how these creatures evolved.
    [Show full text]
  • Sustainability of Threatened Species Displayed in Public Aquaria, with a Case Study of Australian 1 Sharks and Rays 2 3 Kathryn
    https://link.springer.com/article/10.1007/s11160-017-9501-2 1 PREPRINT 1 Sustainability of threatened species displayed in public aquaria, with a case study of Australian 2 sharks and rays 3 4 Kathryn A. Buckley • David A. Crook • Richard D. Pillans • Liam Smith • Peter M. Kyne 5 6 7 K.A. Buckley • D.A. Crook • P.M. Kyne 8 Research Institute for the Environment and Livelihoods, Charles Darwin University, Darwin, NT 0909, 9 Australia 10 R.D. Pillans 11 CSIRO Oceans and Atmosphere, 41 Boggo Road, Dutton Park, QLD 4102, Australia 12 L. Smith 13 BehaviourWorks Australia, Monash Sustainable Development Institute, Building 74, Monash University, 14 Wellington Road, Clayton, VIC 3168, Australia 15 Corresponding author: K.A. Buckley, Research Institute for the Environment and Livelihoods, Charles Darwin 16 University, Darwin, NT 0909, Australia; Telephone: +61 4 2917 4554; Fax: +61 8 8946 7720; e-mail: 17 [email protected] 18 https://www.nespmarine.edu.au/document/sustainability-threatened-species-displayed-public-aquaria-case-study-australian-sharks-and https://link.springer.com/article/10.1007/s11160-017-9501-2 2 PREPRINT 19 Abstract Zoos and public aquaria exhibit numerous threatened species globally, and in the modern context of 20 these institutions as conservation hubs, it is crucial that displays are ecologically sustainable. Elasmobranchs 21 (sharks and rays) are of particular conservation concern and a higher proportion of threatened species are 22 exhibited than any other assessed vertebrate group. Many of these lack sustainable captive populations, so 23 comprehensive assessments of sustainability may be needed to support the management of future harvests and 24 safeguard wild populations.
    [Show full text]
  • Etyfish Orectolobifo
    ORECTOLOBIFORMES (Carpet Sharks) · 1 The ETYFish Project © Christopher Scharpf and Kenneth J. Lazara COMMENTS: v. 7.0 - 15 Oct. 2019 Order ORECTOLOBIFORMES Carpet Sharks 7 families · 13 genera · 45 species Family PARASCYLLIIDAE Collared Carpet Sharks 2 genera · 8 species Cirrhoscyllium Smith & Radcliffe 1913 cirrus, curl or tendril, referring to barbels on throat; skylion, Greek for dogfish or small shark, probably from skyllo, to tear or mangle Cirrhoscyllium expolitum Smith & Radcliffe 1913 varnished, referring to how the shark’s body, when dry, “glistens as though varnished, owing to the peculiar character of the dermal denticles” Cirrhoscyllium formosanum Teng 1959 -anum, adjectival suffix: referring to distribution off the coast of Formosa (Taiwan) Cirrhoscyllium japonicum Kamohara 1943 Japanese, known only from Mimase, Shikoku, Japan Parascyllium Gill 1862 para-, near, i.e., related to Scylliorhinus (now in Scyliorhinidae); skylion, Greek for dogfish or small shark, probably from skyllo, to tear or mangle Parascyllium collare Ramsay & Ogilby 1888 collar, referring to prominent dark and unspotted collar around gills Parascyllium elongatum Last & Stevens 2008 prolonged, referring to distinctive, elongate body shape Parascyllium ferrugineum McCulloch 1911 rust-colored, referring to dark brown spots on sides and fins Parascyllium sparsimaculatum Goto & Last 2002 sparsi, sparse; maculatum, spotted, referring to relatively larger (and hence fewer) spots than congeners Parascyllium variolatum (Duméril 1853) spotted, referring to white
    [Show full text]
  • Locomotion Is Not a Privilege After Birth: Ultrasound Images of Viviparous Shark Embryos Swimming from One Uterus to the Other
    Received: 22 July 2018 | Revised: 14 September 2018 | Accepted: 24 October 2018 DOI: 10.1111/eth.12828 BEHAVIOURAL NOTE Locomotion is not a privilege after birth: Ultrasound images of viviparous shark embryos swimming from one uterus to the other Taketeru Tomita1,2 | Kiyomi Murakumo2 | Keiichi Ueda1,2 | Hiroshi Ashida2 | Rina Furuyama2 1Okinawa Churashima Research Center, Okinawa Churashima Foundation, Abstract Motobu, Japan Underwater ultrasound, a new tool for observing the internal body parts of aquatic 2 Okinawa Churaumi Aquarium, Motobu, animals by scuba divers, allowed us long‐term and frequent observations of the em‐ Japan bryos of captive aquatic vertebrates. New ultrasound data of captive tawny nurse Correspondence sharks (Nebrius ferrugineus) revealed that their embryos frequently migrate between Taketeru Tomita, Okinawa Churashima Research Center, Okinawa Churashima the right and left uteri during gestation. This report is the first reliable evidence of Foundation, Motobu, Japan. active embryonic locomotion in live‐bearing vertebrates and is contradictory to the Email: t‐[email protected] concept of “sedentary embryo” which has mainly arisen from studies of mammals. Funding information The tawny nurse shark is unique among orectolobiform sharks, in which the embryo Okinawa Churaumi Aquarium develops by feeding on sibling eggs in utero. Thus, we hypothesized that swimming Editor: R. Bshary aids in an efficient search and capture of these eggs in the uterine environment. KEYWORDS captivity, diagnostic sonography, elasmobranch, nurse shark, oophagy, viviparity 1 | INTRODUCTION 2016; Tomita, Toda, Uchida, & Nakaya, 2012; Tomita et al., 2018). However, ultrasound devices cannot be used underwater, and spec‐ Locomotion, the ability of body displacement, by swimming, walking, imens should be kept near the surface of the water during obser‐ or flying, is one of the defining characteristics of animals (Biewener, vation.
    [Show full text]
  • And Their Functional, Ecological, and Evolutionary Implications
    DePaul University Via Sapientiae College of Science and Health Theses and Dissertations College of Science and Health Spring 6-14-2019 Body Forms in Sharks (Chondrichthyes: Elasmobranchii), and Their Functional, Ecological, and Evolutionary Implications Phillip C. Sternes DePaul University, [email protected] Follow this and additional works at: https://via.library.depaul.edu/csh_etd Part of the Biology Commons Recommended Citation Sternes, Phillip C., "Body Forms in Sharks (Chondrichthyes: Elasmobranchii), and Their Functional, Ecological, and Evolutionary Implications" (2019). College of Science and Health Theses and Dissertations. 327. https://via.library.depaul.edu/csh_etd/327 This Thesis is brought to you for free and open access by the College of Science and Health at Via Sapientiae. It has been accepted for inclusion in College of Science and Health Theses and Dissertations by an authorized administrator of Via Sapientiae. For more information, please contact [email protected]. Body Forms in Sharks (Chondrichthyes: Elasmobranchii), and Their Functional, Ecological, and Evolutionary Implications A Thesis Presented in Partial Fulfilment of the Requirements for the Degree of Master of Science June 2019 By Phillip C. Sternes Department of Biological Sciences College of Science and Health DePaul University Chicago, Illinois Table of Contents Table of Contents.............................................................................................................................ii List of Tables..................................................................................................................................iv
    [Show full text]
  • Migratory Sharks Complete 3 0 0.Pdf
    CMS Technical Series No. 15 Review of Migratory Chondrichthyan Fishes Review of Migratory Chondrichthyan Fishes Prepared by the Shark Specialist Group of the IUCN Species Survival Commission on behalf of the CMS Secretariat • CMS Technical Series No. 15 CMS Technical UNEP/CMS Secretariat Public Information Hermann-Ehlers-Str. 10 53113 Bonn, Germany T. +49 228 815-2401/02 F. +49 228 815-2449 www.cms.int Review of Chondrichthyan Fishes IUCN Species Survival Commission’s Shark Specialist Group December 2007 Published by IUCN–The World Conservation Union, the United Nations Environment Programme (UNEP) and the Secretariat of the Convention on the Conservation of Migratory Species of Wild Animals (CMS). Review of Chondrichthyan Fishes. 2007. Prepared by the Shark Specialist Group of the IUCN Species Survival Commission on behalf of the CMS Secretariat. Cover photographs © J. Stafford-Deitsch. Front cover: Isurus oxyrinchus Shortfin mako shark. Back cover, from left: Sphyrna mokarran Great hammerhead shark, Carcharodon carcharias Great white shark, Prionace glauca Blue shark. Maps from Collins Field Guide to Sharks of the World. 2005. IUCN and UNEP/ CMS Secretariat, Bonn, Germany. 72 pages. Technical Report Series 15. This publication was prepared and printed with funding from the CMS Secretariat and Department for the Environment, Food, and Rural Affairs, UK. Produced by: Naturebureau, Newbury, UK. Printed by: Information Press, Oxford, UK. Printed on: 115gsm Allegro Demi-matt produced from sustainable sources. © 2007 IUCN–The World Conservation Union / 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.
    [Show full text]
  • 3. List of Species by Major Fishing Areas
    click for previous page 210 FAO Species Catalogue for Fishery Purposes No. 1 3. LIST OF SPECIES BY MAJOR FISHING AREAS p GEOGRAPHICAL DISTRIBUTION a Major Areas for Statistical Purposes Species g Fresh 18 21 27 31 34 37 41 47 48 51 57 58 61 67 71 77 81 87 88 e water ARC WNA ENA WCA ECA MED WSA ESA ANC WIO EIO ANE WNP ENP WCP ECP WSP ESP ANW Alopias pelagicus 81 · ·· · ···· Alopias superciliosus 83 ······· ·· · · · ·· Alopias vulpinus 86 ·········· ··· · ·· Brachaelurus waddi 145 ··· Carcharias taurus 58 ······· ·· · · · Carcharodon carcharias 100 ········ ·· ··· · ·· Cetorhinus maximus 91 ········ · ··· · ·· Chiloscyllium arabicum 167 · Chiloscyllium burmensis 168 · Chiloscyllium griseum 169 ·· · · Chiloscyllium hasselti 171 ··· Chiloscyllium indicum 172 ·· · · Chiloscyllium plagiosum 173 ·· · · Chiloscyllium punctatum 175 ·· · · Cirrhoscyllium expolitum 133 ·· Cirrhoscyllium formosanum 134 · Cirrhoscyllium japonicum 135 · Eucrossorhinus dasypogon 151 ·· Ginglymostoma cirratum 192 ······ · · Hemiscyllium freycineti 179 · Hemiscyllium hallstromi 180 · Hemiscyllium ocellatum 181 ··· Hemiscyllium strahani 182 · Hemiscyllium trispeculare 183 ·· Heterodontus francisci 36 ·· Heterodontus galeatus 38 ··· Heterodontus japonicus 39 · Heterodontus mexicanus 41 · Heterodontus portusjacksoni 42 ··· Heterodontus quoyi 45 · Heterodontus ramalheira 46 · Heterodontus sp. A 49 · Heterodontus zebra 48 ··· Heteroscyllium colcloughi 147 · Isurus oxyrinchus 109 ······· ·· ··· · ·· Isurus paucus 115 ······· ·· · · · · Lamna ditropis 119 ···· Lamna nasus 121
    [Show full text]
  • Stegostoma Fasciatum (Hermann, 1783) Fig
    click for previous page 186 FAO Species Catalogue for Fishery Purposes No. 1 Stegostoma fasciatum (Hermann, 1783) Fig. 156 Squalus fasciatus Hermann, 1783, Tab. Affin.: 302. Based on Squalus varius Seba, 1758. A senior homonym of Squalus fasciatus Bonnaterre, 1788 = Poroderma africanum (Gmelin, 1788). No types according to Eschmeyer (1998, Cat. Fish.: CD-ROM). Also, Squalus fasciatus Bloch, 1785, Naturg. Ausl. Fische, 1: 19, pl. 113. Holotype: Zoologisches Museum, Museum für Naturkunde der Humboldt-Universität, Berlin, ZMB-4449, 355 mm total length male, Indian Ocean from Tranquebar, according to Paepke and Schmidt (1988, Mitt. Zool. Mus. Berlin, 64(1): 163). Synonyms: Squalus varius Seba, 1758: 105, pl. 34, fig. 1. No type locality or specimens. Name not available because Seba’s usage of nomenclature was not consistently binomial (see remarks above). Squalus tigrinus Pennant, 1769: 24; (nomen nudum?). Squalus tygrinus Bonnaterre, 1788: 8, pl. 8, fig. 23. Type material uncertain. Type locality: “La mer des Indes”. Squalus tigrinus Gmelin, in Linnaeus and Gmelin, 1788: 1493. Type material uncertain. Type locality: “Oceano indico”. Squalus varius Seba, 1758 included in synonymy. This species was probably based on juveniles with a striped colour pattern. Squalus longicaudatus Gmelin, in Linnaeus and Gmelin, 1788: 1496. Type material uncertain, no locality given. Squalus varius Seba, 1758 included in synonymy. This was not strongly distinguished from S. tigrinus, but may have been based on post-juveniles with a spotted colour pattern. Scyllia quinquecornuatum van Hasselt, 1823: 15. Reference to Squalus varius Seba, 1758, and presumably a replacement name for it. No types listed in Eschmeyer (1998: CD-ROM).
    [Show full text]
  • Carpet Sharks
    click for previous page 126 FAO Species Catalogue for Fishery Purposes No. 1 2.3 Order ORECTOLOBIFORMES - Carpet sharks Order: Orectolobiformes: Compagno, 1973, J. Linn. Soc. (Zool.), 53, suppl. 1: 28; also Applegate, 1974, J. Mar. Biol. Ass. India, 14(2): 743. Number of Recognized Families: 7. Synonyms: [Part] 1 Squali, Abtheilung [Division] 1: Müller and Henle, 1838d: 3. [Part] 1 Squali, Abtheilung [Division] 2, Unterabtheilung [Subdivision] 3: Müller and Henle, 1839: 66. Ordo Plagiostomi, Subordo Squalini, Sectio Proktopterides, Tribus Dinotopterini: Bleeker, 1859: xi. Order Squali, Suborder Squali: Gill, 1862b: 394, 396. Order Squali, Suborder Galei: Gill, 1872: 22, 23. Order Plagiostomi diplospondyli, Suborder Plagiostomi asterospondyli, Group 1 Scyllia: Hasse, 1879: 52. Order Plagiostomi diplospondyli, Suborder Plagiostomi asterospondyli, Group 2 Scylliolamnidae: Hasse, 1879: 51. Order Selachii, Suborder Asterospondyli: Woodward, 1889: 157. Order Asterospondyli, suborder unnamed: Gill, 1893: 130; Fowler, 1941: 4, 13; Smith, 1949: 37, 39. Order Asterospondyli, Suborder Galei: Jordan and Evermann, 1896: 19, 21. Order Euselachii, Suborder Pleurotremata, Division Galeoidei: Regan, 1906a: 723. Order Selachii, Group 2, Division B, Subdivision 1, Suborder Scylliodei: Goodrich, 1909: 148. Order Pleurotremata, Suborder Galeoidei: Engelhardt, 1913: 97. Order Plagiostoma, Suborder Antacea, “Group” Catuloidei: Garman, 1913: 11, 12. Order Plagiostoma, Suborder Antacea, “Group” Isuroidei: Garman, 1913: 10, 12. Order Euselachii, Suborder Galei, [Series] Scyllioidei: Jordan, 1923: 97. Order Plagiostomi, Suborder Galeiformes: Lozano y Rey, 1928: 280. Order Galea, Suborder Isurida, Superfamily Orectoloboidea: White, 1936: 4; White, 1937: 36, tab. 1. Order Euselachii, Suborder Scylliformes: Bertin, 1939a: 9. Order Lamniformes, Suborder Lamnoidei: Berg, 1940: 137; Berg and Svetovidov, 1955: 65; Patterson, 1967: 670; Lindberg, 1971: 8, 257; Nelson, 1976: 33; Nelson, 1984: 51.
    [Show full text]
  • Hemiscylliidae 1249
    click for previous page Hemiscylliidae 1249 HEMISCYLLIIDAE Longtail carpetsharks by L.J.V. Compagno and V.H. Niem iagnostic characters: Small sharks. Trunk cylindrical or moderately depressed, precaudal tail Dcylindrical and somewhat longer than head and trunk, lateral ridges on sides of trunk and tail present or absent. Head not expanded laterally, cylindrical or moderately depressed; 5 small gill slits present, the last 3 over the pectoral-fin base, their upper ends not expanded onto upper surface of head; no gill sieves or rakers on internal gill slits; spiracles very large and located behind and below eyes; nostrils with barbels, nasoral grooves, and circumnarial grooves, close in front of mouth; eyes above and medial to sides of head, without nictitating eyelids; snout short to moderately long, slightly depressed, parabolic to broadly rounded, not greatly flattened and blade-like and without lateral teeth or barbels; mouth small, nearly transverse, and well in front of eyes, without a symphyseal groove on chin; labial furrows present on both jaws and relatively large, with upper furrows extending in front of mouth; teeth small, not blade-like, with a single cusp on upper and lower teeth and with cusplets small or absent; teeth similar in both jaws, not differentiated into medials, anteriors, intermediates, laterals, or posteriors. Two dorsal fins without spines, the first moderate sized, subangular, much shorter than the caudal fin, and with its origin over or behind the pelvic-fin bases; second dorsal fin about as large as the first and of similar shape; anal fin moderately large, very low, broad and rounded, with its origin well behind the second dorsal-fin base and its base separated by a notch from the caudal fin; caudal fin strongly asymmetrical, much less than 1/2 of total length, without a rippled dorsal margin or lower lobe but with a strong subterminal notch; vertebral axis of caudal fin hardly raised above body axis.
    [Show full text]
  • Shark and Ray By-Catch
    ASSESSING SHARK AND RAY BYCATCH IN INDONESIAN DEEPWATER SNAPPER- GROUPER FISHERIES Report on data analysis January 2017 - December 2018 Project ID: P104884 Prepared for The Nature Conservancy Indonesia by Steven Lindfield and Vanessa Jaiteh Coral Reef Research Foundation October, 2019 ASSESSING SHARK AND RAY BYCATCH IN INDONESIAN SNAPPER-GROUPER FISHERIES 1. BACKGROUND AND OBJECTIVES The purpose of this work is to assess shark and ray bycatch in Indonesian deep-water snapper and grouper fisheries. Since 2014, The Nature Conservancy (TNC) has been working with a number of Indonesian deep-slope (50-500 m) dropline and demersal longline fisheries that target various snapper, grouper and emperorfish species. These fisheries are currently being monitored using a Crew-Operated Data Recording System (CODRS) which provides photographs of all target and non-target catch. This monitoring program is organized through TNC’s Indonesia field office to support the development and adoption of data-poor stock assessment approaches with involvement of the private sector in data collection. Following the application of CODRS, TNC has gained information not only on the snapper, grouper, and emperorfish fishery but also its shark and ray bycatch. Globally, one quarter of all shark and ray species are currently threatened with extinction mainly due to their capture in target fisheries and as bycatch in other fisheries. In the last decade, government and non-government organizations have widely adopted conservation efforts to restore threatened shark populations, but these efforts are often hindered by a lack of comprehensive and accurate data. This report assesses shark and ray bycatch through the development of a species list (according to species-level identification of the catch based on photographs that the crew take aboard fishing vessels).
    [Show full text]
  • Investigating the Mysteries of Reproduction
    Reproduction of Marine Life, Birth of New Life! Investigating the Mysteries of Reproduction A primer on shark reproduction for aquarists Jose I. Castro NOAA, Southeast Fisheries Science Center, 75 Virginia Beach Drive, Miami, Florida 33149, USA Contact e-mail: [email protected] Introduction Aquariums are one of the most popular and profitable public entertainment enterprises, and sharks are invariably one of their most popular and prized exhibits. Unfortunately, due to a variety or reasons, sharks are among the most difficult species to maintain in captivity. Only a few species can be maintained for long periods and even fewer reproduce in captivity. Some small catsharks have been maintained in aquaria for many successive generations, and a few large species, such as the sand tiger shark and the nurse shark can survive in captivity for decades. The larger species are generally difficult to maintain in captivity, and most survive in present day aquariums only for short periods of days or weeks, or at best a few months. The goal of most aquarists, and the final test of successful aquarium husbandry, is to provide a captive environment where a species can attain its full life span and reproduce successfully, engendering successive captive generations. The purpose of this paper is to provide a primer on shark reproduction for aquarists, to help in understanding the reproductive processes of the sharks they keep and to provide a framework for aquarists to make observations that will contribute to our understanding of the reproductive biology of sharks. Because of the difficulties of studying and observing sharks in the natural environment, much can be learned in the aquarium, and aquarists can contribute significantly to our knowledge of sharks when their observations are systematically recorded and subsequently published.
    [Show full text]