Tierbestandsliste 2015.Pdf

Total Page:16

File Type:pdf, Size:1020Kb

Tierbestandsliste 2015.Pdf Tierbestandsliste 31.12.2015 AMPHIBIEN AMPHIBIA AMPHIBIENS BLINDWÜHLEN GYMNOPHIONA CAECILIANS Schwimmwühle Typhlonectes compressicauda Aquatic caecilian Schwimmwühle Typhlonectes natans SCHWANZLURCHE CAUDATA SALAMANDERS Ambystomatidae Axolotl Ambystoma mexicanum Axolotl Salamandridae Feuersalamander Salamandra salamandra European fire salamander Feuersalamander Salamandra s. terrestris Zagros-Molch Neurergus kaiseri Sirenidae Großer Armmolch Siren lacertina FROSCHLURCHE ANURA FROGS Discoglossidae Gelbbauchunke Bombina variegata variegata Yellow bellied toad Pelobatidae Knoblauchkröte Pelobates fuscus Megophryidae Zipfelkrötenfrosch Megophrys nasuta Bufonidae Coloradokröte Bufo alvarius Colorado toad Erdkröte Bufo bufo Common toad Kreuzkröte Bufo calamita Natterjack Tropfenkröte Bufo guttatus Aga-Kröte Bufo marinus Wechselkröte Bufo viridis Green toad 1 Tierbestandsliste 31.12.2015 Eleutherodactylidae Gewächshausfrosch Eleutherodactylus planirostris Dendrobatidae Grüngestr.Riesenbaumsteiger Ameeraga trivittata Three lined poison arrow frog Goldbaumsteiger Dendrobates auratus Green and black poison arrow frog Schwarzgelber Baumsteiger Dendrobates leucomelas Färberfrosch Dendrobates t. alanis Blauer Färberfrosch Dendrobates tinc. azureus Blue poison arrow frog Färberfrosch Dendrobates t.Graubeiner Dreistreifen-Baumsteiger Epipedobates anthonyi Maranon-Baumsteiger Excidobates mysteriosus Goldener Pfeilgiftfrosch Phyllobates terribilis Hylidae Beutelfrosch Gastrotheca riobambae Korallenfinger Litoria caerulea White's tree frog Riesenlaubfrosch Litoria infrafrenata Riesen-Makifrosch Phyllomedusa bicolor Baumhöhlen-Krötenlaubfrosch Trachycephalus resinifictrix Striped tree frog Ranidae Teichfrosch Rana esculenta Edible frog Ochsenfrosch Rana catesbeiana Rhacophoridae Weißbart-Ruderfrosch Polypedates leucomystax Asian tree frog Moosfrosch Theloderma corticale Microhylidae Gefleckter Tomatenfrosch Dyscophus guineti Tomato frog 2 Tierbestandsliste 31.12.2015 FISCHE PISCES FISHES CHIMAERIFORMES Chimaeridae Gefleckte Seeratte Hydrolagus colliei spotted ratfish HETERODONTIFORMES Heterodontidae Stierkopfhai Heterodontus francisci Hornshark CARCHARHINIFORMES Scyliorhinidae Kleingefleckter Katzenhai Scyliorhinus canicula Lesser Spotted Dogfish Großgefleckter Katzenhai Scyliorhinus stellaris Spotted Dogfish Triakidae Leopardenhai Triakis semifasciata Leopard Shark RAJIFORMES Rajidae Nagelrochen Raja clavata Dasyatidae Blaupunkt-Maskenrochen Neotrygon kuhlii Blue-spotted maskray DIPNOI (Sarcopterygii) Ceratodontidae Australischer Lungenfisch Neoceratodes forsteri Australian Lungfish Protopteridae Afrikanischer Lungenfisch Protopterus aethiopicus West-African Lungfish 3 Tierbestandsliste 31.12.2015 POLYPTERIFORMES Polypteridae Flösselaal Erpetoichthys calabaricus Eel Bichir Guinea-Flösselhecht Polypterus ansorgii Schmuckflösselhecht Polypterus ornatipinnis Ornate Bichir Senegal-Flösselhecht Polypterus senegalus Gray bichir ACIPENSERIFORMES Acipenseridae Sterlet Acipenser ruthenus Sterlet LEPISOSTEIFORMES Lepisosteidae Alligatorhecht Atractosteus spatula Alligator Gar Kuba-Alligatorhecht Atractosteus tristoechus Pike Gar Gefleckter Knochenhecht Lepisosteus oculatus Spotted Gar OSTEOGLOSSIFORMES Arapaimidae Arapaima Arapaima gigas Osteoglossidae Malaiischer Knochenzüngler Scleropages formosus Asian Arrowana Pantodontidae Schmetterlingsfisch Pantodon buchholzi Butterflyfish Notopteridae Afrikanischer Messerfisch Xenomystus nigri Apteronotidae Weißstirn-Messerfisch Apteronotus albifrons Mormyridae Tapirfisch Gnathonemus petersii Zwergnilhecht Pollimyrus castelnaui 4 Tierbestandsliste 31.12.2015 ANGUILLIFORMES Anguillidae Aal Anguilla anguilla European Eel Muraenidae Sternmuräne Echidna nebulosa Panthermuräne Enchelycore pardalis Zebramuräne Gymnomuraena zebra Zebra Moray Mitelmeermuräne Muraena helena Weiße Bandmuräne Pseudechidna brummeri Nasenmuräne Rhinomuraena quaesita Congridae Ohrenfleck-Röhrenaal Heteroconger hassi Garden eel CYPRINIFORMES Cyprinidae Brachse Abramis brama Bream Schneider Alburnoides bipunctatus Ukelei Alburnus alburnus Rapfen Aspius aspius Haibarbe Balantiocheilus melanopterus Brassenbarbe Barbonymus schwanenfeldii Barbe Barbus barbus Barbel Blaustrichbarbe Barbus barilioides Sumatrabarbe Barbus tetrazona Tiger Barb Bitterlingsbarbe Barbus titteya Cherry Barb Güster Blicca bjoerkna White Bream Steinroller Campostoma anomalum Stoneroller Karausche Carassius carassius Crucian Carp Giebel Carassius gibelio Nase Chondrostoma nasus Nosed Minnow Rotstreifen-Elritze Clinostomus elongatus Redside dace Siamesische Rüsselbarbe Crossocheilus siamensis Barbel Graskarpfen Ctenopharyngodon idella Schuppenkarpfen Cyprinus carpio Carp Spiegelkarpfen Cyprinus carpio var. German Carp Farbkarpfen, Koi Cyprinus carpio var. Koi Malabarbärbling Danio malabaricus Giant Danio Feuerschwanz-Fransenlipper Epalzeorhynchus bicolor Gründling Gobio gobio Gudgeon Moderlieschen Leucaspius delineatus Döbel Leuciscus cephalus 5 Tierbestandsliste 31.12.2015 Hasel Leuciscus leuciscus Dace Regenbogenelritze Notropis chrosomus Rainbow shiner Javakarpfen, Nilem Osteochilus vittatus Elritze Phoxinus phoxinus Minnow Rotstrichbarbe Puntius denisonii Schönflossenbärbling Rasbora kalochroma Bitterling Rhodeus amarus Bitterling Plötze Rutilus rutilus Roach Rotfeder Scardinius erythrophthalmus Rudd Strömer Telestes souffia Schleie Tinca tinca Hengels Bärbling Trigonostigma hengeli Gyrinocheilidae Siamesiche Saugschmerle Gyrinocheilus aymonieri Balitoridae Bachschmerle Barbatula barbatula Punktierter Flossensauger Gastromyzon punctulatus Cobitidae Pferdekopfschmerle Acantopsis choirorhynchos Tigerschmerle Botia helodes Schachbrettschmerle Botia sidthimunki Prachtschmerle Chromobotia macracantha Clown Loach Steinbeißer Cobitis taenia CHARACIFORMES Lebiasinidae Spitzmaul-Ziersalmler Nannostomus eques Pencill Tetra Characidae Großschuppensalmler Arnoldichthys spilopterus Silbersalmler Astyanax fasciatus Mexican Tetra Blinder Höhlensalmler Astyanax fasciatus mexican. Blind Cave Tetra Trauermantelsalmler Gymnocorymbus ternetzi Rotmaulsalmler Hemigrammus rhodostomus Kirschflecksalmer Hyph. erythrostigma Sailfin Tetra Zitronensalmler Hyphessobrycon pulchripinnis Blutsalmler Hyphessobrycon serpae Socolofs Kirschflecksalmler Hyphessobrycon socolofi Scheibensalmler Myleus duriventre Haken-Scheibensalmler Myleus rubripinnis Schomburgks Scheibensalmler Myleus schomburgki 6 Tierbestandsliste 31.12.2015 Kaisersalmler Nematobrycon palmeri Roter Neon Paracheirodon axelrodi Neon Tetra Rotkopfsalmler Petitella georgiae Kongo-Salmler Phenacogrammus interruptus Congo Characin Pacu Piaractus brachypomus Sternfleckensalmler Pristella maxillaris Piranha Pygocentrus nattereri Redbelly Piranha Hemiodontidae Federsalmler Hemiodus gracilis Torpedo Tetra Curimatidae Nachtsalmler Semaprochilodus taeniurus Gasteropelecidae Gestreifter Beilbauch Carnegiella marthae Marmorierter Beilbauch Carnegiella strigata Marbled Hatchedfish Anostomidae Prachtkopfsteher Anostomus anostomus Striped Anostomus Gebänderter Kopfsteher Leporinus fasciatus SILURIFORMES Siluridae Indischer Glaswels Kryptopterus vitreolus Glass Catfisch Waller Silurus glanis Schilbeidae Schwalbenschwanz-Glaswels Pareutropius buffei Kongoglaswels Pareutropius debauwi Pangasiidae Haiwels Pangasius pangasius Catfish Haiwels Pangasius sutchi Mochocidae Rückenschw. Kongowels Synodontis nigriventris Upside-down Catfish Schwarzgefl. Fiederbartwels Synodontis nigromaculatus Augenflecken-Fiederbartwels Synodontis ocellifer Doradidae Liniendornwels Platydoras costatus Schwarzer Dornenwels Pseudodoras niger 7 Tierbestandsliste 31.12.2015 Pimelodidae Segelantennenwels Leiarius pictus Rotschwanzwels Phractocephalus hemiliopt. Engel-Antennenwels Pimelodus pictus Catfish Tigerspatelwels Pseudoplatystoma fasciatum Zungarowels Zungaro zungaro Gilded catfish Callichthyidae Metall-Panzerwels Corydoras aeneus Cope's Panzerwels Corydoras copei Zweifarben-Panzerwels Corydoras melini Two-coloured corydoras Getüpfelter Panzerwels Corydoras punctatus Sterbas Panzerwels Corydoras sterbai Loricariidae Elfenwels Acanthicus adonis Antennen-Schilderwels Ancistrus multispinis Blue-chin Catfish Gelbsaumwels Baryancistrus sp. (L 81) Nadelwels Farlowella acus Zebra-Harnischwels Hypancistrus spec L 129 Schneeflockenwels Lasiancistrus sp. (L33) Peru-Riesenschilderwels Liposarcus pardalis Ohrgitter-Harnischwels Otocinclus affinis Ringelsocken-Harnischwels Panaqolus albivermis Zwergschilderwels Panaqolus sp. (L2) Gestreifter Harnischwels Panaque nigrolineatus Catfish Schmucklinien-Zwergschilderwels Peckoltia compta L 134 Zweibinden-Zwergschilderwels Peckoltia vittata Wabenschilderwels Pterygoplichthys gibbiceps Maulbrütender Harnischwels Pyxiloricaria sp. Goldbartelwels Sturisoma aureum GYMNOTIFORMES Electrophoridae Zitteraal Electrophorus electricus Electric Eel ESOCIFORMES Esocidae Hecht Esox lucius Pike 8 Tierbestandsliste 31.12.2015 SALMONIFORMES Salmonidae Huchen Hucho hucho Bachforelle Salmo trutta Brown Trout Bachsaibling Salvelinus fontinalis Charr Äsche Thymallus thymallus BATRACHOIDIFORMES Batrachoididae Lusitanischer Krötenfisch Halobatrachus didactylus Lusitanian toadfish GADIFORMES Gadidae Kabeljau Gadus morrhua Atlantic Cod Trüsche Lota lota Pollack Pollachius pollachius Köhler Pollachius virens Franzosendorsch Trisopterus luscus Tacaud LOPHIIFORMES Antennariidae Anglerfisch Antennarius maculatus MUGILIFORMES Mugilidae Dicklippige Meeräsche Mugil chelo Mullet ATHERINIFORMES Melanotaeniidae Lachsroter Regenbogenfisch Glossolepis incisus Rainbow Fish Prachtährenfisch
Recommended publications
  • Fishes of the Deep Demersal Habitat at Ngazidja (Grand Comoro) Island, Western Indian Ocean
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by South East Academic Libraries System (SEALS) 444 South African Journal of Science 102, September/October 2006 Coelacanth Research Fishes of the deep demersal habitat at Ngazidja (Grand Comoro) Island, Western Indian Ocean Phillip C. Heemstraa*, Karen Hissmannb, Hans Frickeb, Malcolm J. Smalec and Jürgen Schauerb (with hook and line or traps) in the daytime habitat of the coela- canth, we were able to identify 65 species (Table 1). For various Underwater observations of the coelacanth, Latimeria chalumnae reasons, the remaining taxa are identified only to genus or Smith, 1939, from a research submersible provided opportunities family level. Our list of the deep demersal fish at Ngazidja is to study the deep demersal fish fauna at the Comoro Islands. The obviously incomplete, as we made no attempt to collect small demersal habitat in depths of 150–400 m at the volcanic island of cryptic species (e.g. Scorpaenidae, Callionymidae, Draconettidae, Ngazidja is low in fish diversity and biomass, compared with the Percophidae, Epigonidae and Plectranthias). In addition, larger, shallow-water coral reef habitat of Ngazidja or the deep demersal elusive species (e.g. congrid and ophichthid eels and several habitats of other localities in the Indo-Pacific region. The resident species of sharks) that are known to occur at depths of 150–400 m deep demersal fish fauna at Ngazidja is dominated by the coela- in the Western Indian Ocean but have not yet been seen or canth, an ancient predator that is specially adapted for this caught at these depths at Ngazidja are not included in our low-energy environment.
    [Show full text]
  • FAMILY Monocentridae Gill, 1859 - Pineconefishes [=?Notacandia, Monocentroidae] Notes: Spelling in Prevailing Recent Practice ?Notacandia Rafinesque, 1815:85 [Ref
    FAMILY Monocentridae Gill, 1859 - pineconefishes [=?Notacandia, Monocentroidae] Notes: Spelling in prevailing recent practice ?Notacandia Rafinesque, 1815:85 [ref. 3584] (subfamily) ? Lepisacanthus [as Lepicantha; no stem of the type genus, not available, Article 11.7.1.1] Monocentroidae Gill, 1859b:144 [ref. 1762] (family) Monocentris [also as subfamily Monocentrinae; stem emended to Monocentrid- by Steyskal 1980:170 [ref. 14191]; Eschmeyer 1998:2471 [ref. 23416] and Nelson 2006:301 [ref. 32486] used Monocentridae] GENUS Cleidopus De Vis, 1882 - pineapplefishes [=Cleidopus De Vis [C. W.], 1882:367] Notes: [ref. 1087]. Masc. Cleidopus gloriamaris De Vis 1882. Type by monotypy. •Valid as Cleidopus De Vis 1882 -- (Paxton et al. 1989:364 [ref. 12442], Gomon et al. 1994:411 [ref. 22532], Kotlyar 1996:208 [ref. 23292], Paxton 1999:2214 [ref. 24788], Paxton et al. 2006:766 [ref. 28994], Gomon 2008:433 [ref. 30616]). Current status: Valid as Cleidopus De Vis, 1882. Monocentridae. Species Cleidopus gloriamaris De Vis, 1882 - pineapplefish, knightfish, coat-of-mail fish [=Cleidopus gloriamaris De Vis [C. W.], 1882:368, Cleidopus gloriamaris occidentalis Whitley [G. P.], 1931:314] Notes: [Proceedings of the Linnean Society of New South Wales v. 7 (pt 3); ref. 1087] Brisbane River or Moreton Bay, Queensland, Australia. Current status: Valid as Cleidopus gloriamaris De Vis, 1882. Monocentridae. Distribution: Australia: Queensland and New South Wales (eastern population) and Western Australia. Habitat: marine. (occidentalis) [Australian Zoologist v. 6 (pt 4); ref. 4672] Fremantle, Western Australia. Current status: Synonym of Cleidopus gloriamaris De Vis, 1882. Monocentridae. Habitat: marine. GENUS Monocentris Bloch & Schneider, 1801 - pineconefishes [=Monocentris Bloch [M. E.] & Schneider [J. G.], 1801:100, Ericius Tilesius [W.
    [Show full text]
  • ASFIS ISSCAAP Fish List February 2007 Sorted on Scientific Name
    ASFIS ISSCAAP Fish List Sorted on Scientific Name February 2007 Scientific name English Name French name Spanish Name Code Abalistes stellaris (Bloch & Schneider 1801) Starry triggerfish AJS Abbottina rivularis (Basilewsky 1855) Chinese false gudgeon ABB Ablabys binotatus (Peters 1855) Redskinfish ABW Ablennes hians (Valenciennes 1846) Flat needlefish Orphie plate Agujón sable BAF Aborichthys elongatus Hora 1921 ABE Abralia andamanika Goodrich 1898 BLK Abralia veranyi (Rüppell 1844) Verany's enope squid Encornet de Verany Enoploluria de Verany BLJ Abraliopsis pfefferi (Verany 1837) Pfeffer's enope squid Encornet de Pfeffer Enoploluria de Pfeffer BJF Abramis brama (Linnaeus 1758) Freshwater bream Brème d'eau douce Brema común FBM Abramis spp Freshwater breams nei Brèmes d'eau douce nca Bremas nep FBR Abramites eques (Steindachner 1878) ABQ Abudefduf luridus (Cuvier 1830) Canary damsel AUU Abudefduf saxatilis (Linnaeus 1758) Sergeant-major ABU Abyssobrotula galatheae Nielsen 1977 OAG Abyssocottus elochini Taliev 1955 AEZ Abythites lepidogenys (Smith & Radcliffe 1913) AHD Acanella spp Branched bamboo coral KQL Acanthacaris caeca (A. Milne Edwards 1881) Atlantic deep-sea lobster Langoustine arganelle Cigala de fondo NTK Acanthacaris tenuimana Bate 1888 Prickly deep-sea lobster Langoustine spinuleuse Cigala raspa NHI Acanthalburnus microlepis (De Filippi 1861) Blackbrow bleak AHL Acanthaphritis barbata (Okamura & Kishida 1963) NHT Acantharchus pomotis (Baird 1855) Mud sunfish AKP Acanthaxius caespitosa (Squires 1979) Deepwater mud lobster Langouste
    [Show full text]
  • March 7, 2017
    Volume 61, Issue 3 March 7, 2017 London Aquaria Society Peter DeSouza will be speaking about selective breed- ing using Killies and Bettas as examples. Neocaridina heteropoda "wild" www.planetinverts.com/ Neocaridina_Heteropoda.html Overview: The Neocaridina Heteropoda species is the wild-type invertebrate of the common Red Cherry Shrimp and Yellow Shrimp. Both of the species were selectively bred from this wild-type in order to ob- tain their solid red and solid yellow coloration. This is the original Red Cherry Shrimp and Yellow Shrimp quite simply. Background: The Neocaridina Heteropoda is found in Asia, its exact location is unknown. This wild species has been used by hobbyists to selectively breed color morphs, such as the Red Cherry Shrimp and Yel- low Shrimp. If you look closely at each of the photos you can see some coloration of either yellow or red. Se- lective breeding is done by taking the characteristics, in this case coloration, and breed the wild shrimp that ex- hibit that color over many times. Eventually a solid color is developed after several generations. This must be a very difficult task. The exact amount of generations that it took for the Red Cherry Shrimp and Yellow Shrimp to become fully colored is unknown. Water Parameters: The Neocaridina Heteropoda Shrimp can be housed in many different water pa- rameters. Just like the Red Cherry Shrimp, this species can be kept in a pH range from 6.0 to 8.0, soft and hard water, temperatures from 72F to 84F and in many different soils like ADA Aquasoil and normal gravel.
    [Show full text]
  • Canning Estuary
    DDeevveellooppmmeenntt ooff bbiioottiicc iinnddiicceess ffoorr eessttaabblliisshhiinngg aanndd mmoonniittoorriinngg eeccoossyysstteemm hheeaalltthh ooff tthhee SSwwaann-- CCaannnniinngg EEssttuuaarryy FINAL TECHNICAL REPORT May 2011 Valesini, F.J., Hallett, C.S., Cottingham, A., Hesp, S.A., Hoeksema, S.D., Hall, N.G., Linke, T.E., Buckland, A.J. Prepared for the Swan River Trust, Department of Water and Department of Fisheries 1 2 Development of biotic indices for establishing and monitoring ecosystem health of the Swan- Canning Estuary FINAL TECHNICAL REPORT May 2011 Valesini, F.J., Hallett, C.S., Cottingham, A., Hesp, S.A., Hoeksema, S.D., Hall, N.G., Linke, T.E., Buckland, A.J. Prepared for the Swan River Trust, Department of Water and Department of Fisheries 3 4 Disclaimer The authors have prepared this report in accordance with the usual care and thoroughness of the Centre for Fish and Fisheries Research (CFFR) for the use by the Swan River Trust (SRT), Department of Water (DoW) and Department of Fisheries (DoF) and only those third parties who have been authorised in writing by the CFFR to rely on the report. It is based on generally accepted practices and standards at the time it was prepared. No other warranty, expressed or implied, is made as to the professional advice included in this report. It is prepared in accordance with the scope of work and for the purpose required by the SRT, DoW and DoF. The methodology adopted and sources of information used by the authors are outlined in this report. The authors have made no independent verification of this information beyond the agreed scope of works, and they assume no responsibility for any inaccuracies or omissions.
    [Show full text]
  • Description of Key Species Groups in the East Marine Region
    Australian Museum Description of Key Species Groups in the East Marine Region Final Report – September 2007 1 Table of Contents Acronyms........................................................................................................................................ 3 List of Images ................................................................................................................................. 4 Acknowledgements ....................................................................................................................... 5 1 Introduction............................................................................................................................ 6 2 Corals (Scleractinia)............................................................................................................ 12 3 Crustacea ............................................................................................................................. 24 4 Demersal Teleost Fish ........................................................................................................ 54 5 Echinodermata..................................................................................................................... 66 6 Marine Snakes ..................................................................................................................... 80 7 Marine Turtles...................................................................................................................... 95 8 Molluscs ............................................................................................................................
    [Show full text]
  • National Report on the Fish Stocks and Habitats of Regional, Global
    United Nations UNEP/GEF South China Sea Global Environment Environment Programme Project Facility NATIONAL REPORT on The Fish Stocks and Habitats of Regional, Global, and Transboundary Significance in the South China Sea CAMBODIA Mr. Ing Try Focal Point for Fisheries Fisheries Administration, Ministry of Agriculture, Forestry and Fisheries 186 Norodom Blvd. P.O. Box 582, Phnom Penh, Cambodia NATIONAL REPORT ON FISHERIES - CAMBODIA Table of Contents 1. BACKGROUND ............................................................................................................................1 1.1 OVERVIEW OF CAMBODIA’S FISHERIES SECTOR ......................................................................1 1.1.1 Total catch by fishing area, port of landing or province (by species/species group, 1990 onwards)................................................................................................1 1.1.2 Fishing effort by gear (number of fishing days/number of boats)..............................4 1.1.2.1 Trawl (Khmer name Uon Ohs)......................................................................5 1.1.2.2 Purse seine/ring net (Khmer name Uon Tith)...............................................6 1.1.2.3 Gill net (Khmer name Mong Paehk) .............................................................7 1.1.2.4 Other (push nets, trolling, hand line, long line, trap)...................................10 1.1.3 Economic value of catch (estimated or actual)........................................................12 1.1.4 Importance of the fisheries
    [Show full text]
  • Evaluation of the Diets of Highly Migratory Species in New Zealand Waters
    CCSBT-ERS/1503/11 Evaluation of the diets of highly migratory species in New Zealand waters New Zealand Aquatic Environment and Biodiversity Report No. 116 P.L. Horn S.L. Ballara P.J.H. Sutton L.H. Griggs ISSN 1179-6480 (online) ISBN978-0-478-42300-6 (online) November 2013 Requests for further copies should be directed to: Publications Logistics Officer Ministry for Primary Industries PO Box 2526 WELLINGTON 6140 Email: [email protected] Telephone: 0800 00 83 33 Facsimile: 04-894 0300 This publication is also available on the Ministry for Primary Industries websites at: http://www.mpi.govt.nz/news-resources/publications.aspx http://fs.fish.govt.nz go to Document library/Research reports © Crown Copyright - Ministry for Primary Industries Table of Contents EXECUTIVE SUMMARY 1 1. INTRODUCTION 2 2. METHODS 3 2.1 Fishery data 3 2.2 Environmental data 4 2.3 Data summaries and analyses 4 3. RESULTS 9 3.1 Overall diet composition by species 9 3.2 Detailed diet descriptions 18 3.2.1 Mako shark 18 3.2.2 Porbeagle shark 25 3.2.3 Blue shark 31 3.2.4 Shortsnouted lancetfish 38 3.2.5 Longsnouted lancetfish 43 3.2.6 Moonfish 50 3.2.7 Ray’s bream 56 3.2.8 Butterfly tuna 62 3.2.9 Albacore 68 3.2.10 Yellowfin tuna 75 3.2.11 Southern bluefin tuna 81 3.2.12 Bigeye tuna 87 3.2.13 Swordfish 93 3.3 Anthropogenic material in stomachs 99 3.4 Influence of moon phase on feeding 99 4.
    [Show full text]
  • National Report on the Fish Stocks and Habitats of Regional, Global
    United Nations UNEP/GEF South China Sea Global Environment Environment Programme Project Facility “Reversing Environmental Degradation Trends in the South China Sea and Gulf of Thailand” National Reports on the Fish Stocks and Habitats of Regional, Global and Transboundary Significance in the South China Sea First published in Thailand in 2007 by the United Nations Environment Programme. Copyright © 2007, United Nations Environment Programme 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. UNEP would appreciate receiving a copy of any publication that uses this publication as a source. No use of this publication may be made for resale or for any other commercial purpose without prior permission in writing from the United Nations Environment Programme. UNEP/GEF Project Co-ordinating Unit, United Nations Environment Programme, UN Building, 2nd Floor Block B, Rajdamnern Avenue, Bangkok 10200, Thailand. Tel. +66 2 288 1886 Fax. +66 2 288 1094 http://www.unepscs.org DISCLAIMER: The contents of this report do not necessarily reflect the views and policies of UNEP or the GEF. The designations employed and the presentations do not imply the expression of any opinion whatsoever on the part of UNEP, of the GEF, or of any cooperating organisation concerning the legal status of any country, territory, city or area, of its authorities, or of the delineation of its territories or boundaries. Cover Photo: Coastal fishing village of Phu Quoc Island, Viet Nam by Mr. Christopher Paterson.
    [Show full text]
  • Urochordata, Pyuridae
    A preliminary evaluation of the distribution and trophodynamics of demersal fish from Spencer Gulf Report to the South Australian Department for Environment and Heritage SARDI Publication No. F2010/000088-1 SARDI Research Report Series No. 424 David R. Currie and Shirley J. Sorokin SARDI Aquatic Sciences PO Box 120 Henley Beach SA 5022 February 2010 A preliminary evaluation of the distribution and trophodynamics of demersal fish from Spencer Gulf Report to the South Australian Department for Environment and Heritage David R. Currie and Shirley J. Sorokin February 2010 SARDI Publication No. F2010/000088-1 SARDI Research Report Series No. 424 Currie, D.R. and Sorokin, S.J. (2010) Trophodynamics of fish from Spencer Gulf This Publication may be cited as: Currie, D.R. and Sorokin, S.J. (2010). A preliminary evaluation of the distribution and trophodynamics of demersal fish from Spencer Gulf. Report to the South Australian Department for Environment and Heritage. South Australian Research and Development Institute (Aquatic Sciences), Adelaide. SARDI Publication No. F2010/000088-1. South Australian Research and Development Institute SARDI Aquatic Sciences 2 Hamra Avenue West Beach SA 5024 Telephone: (08) 8207 5400 Facsimile: (08) 8207 5406 http://www.sardi.sa.gov.au DISCLAIMER The authors warrant that they have taken all reasonable care in producing this report. The report has been through the SARDI internal review process, and has been formally approved for release by the Chief of Division. Although all reasonable efforts have been made to ensure quality, SARDI does not warrant that the information in this report is free from errors or omissions.
    [Show full text]
  • Towards a System of Ecologically Representative Marine Protected
    10 Notes on Current Protection and Management within Recommended Areas _____ 452 10.1 Nuyts Archipelago, St Francis Isles and Coastal Embayments (Murat Bioregion) ____________452 10.2 Baird Bay to Cape Bauer (including nearshore islands) (Murat/Eyre Bioregions Boundary) ___453 10.3 Venus Bay and Surrounds (Eyre Bioregion) ___________________________________________453 10.4 Investigator Group of Islands (Eyre Bioregion) ________________________________________454 10.5 Thorny Passage (Eyre Bioregion) ____________________________________________________455 10.6 Sir Joseph Banks Group and Dangerous Reef (including Tumby Bay) (Eyre Bioregion) ______455 10.7 Neptune Islands Group (Eyre Bioregion) _____________________________________________456 10.8 Gambier Islands Group (Eyre Bioregion) _____________________________________________456 10.9 Franklin Harbor and Surrounding Waters (Spencer Gulf/North Spencer Gulf Bioregions Boundary) ___________________________________________________________________________457 10.10 Upper Spencer Gulf (North Spencer Gulf Bioregion)___________________________________457 10.11 South-Eastern Spencer Gulf (Spencer Gulf Bioregion) _________________________________459 10.12 Western Investigator Strait, between the “Toe” of Yorke Peninsula and Northern Kangaroo Island (Eyre/Gulf St Vincent Biregion Boundary)___________________________________________460 10.13 North-Western, Western and South-Western Kangaroo Island (Eyre Region)______________461 10.14 Southern Eyre (Eyre Bioregion) ____________________________________________________461
    [Show full text]
  • Bioluminescence
    FAU Institutional Repository http://purl.fcla.edu/fau/fauir This paper was submitted by the faculty of FAU’s Harbor Branch Oceanographic Institute. Notice: © 2008 Science Publishers. This manuscript is an author version with the final publication available and may be cited as: Suntsov, A. V., Widder, E. A., & Sutton, T. T. (2008). Bioluminescence. In R. N. Finn, & B. G. Kapoor (Eds.), Fish larval physiology (pp. 51-88). Enfield, NH: Science Publishers. ---------------:--:---:---.,----,-,C HA PTE R ....... ·•···.. ·.._.~ Bioluminescence Andrey V Suntsov\ Edith A Widder-2·• and Tracey T Sutton3 INTRODUCTION The production ofliving light- bioluminescence, is a widespread but very unevenly distributed phenomenon among living org;mbms. As presently known, some five terrestrial and 14 marine phyla and more than 700 gcnern arc known to have luminous species (Herring, 1987; Herring & Widder, 2001). The morphologicnl diversity of luminous organs, physiology and taxonomic occurrence of bioluminescence in fi shes is higher than in any other group of organisms and confim.-d exclusive!~· to marine habitats. A signilkant body ofinfommtil)n on fish bioluminescence is avrJilablc from several derailed reviews (Herring & Morin, 1978; I·!erring, 1982; H aygood, 1993). Hbturicnlly, rhe characterisation of Hsh bioluminescence was almost exclusiwly cunfined tu ndults. As emphasis on early ontoge.ny of fishes has increased in rt~cerH dl:c.nJc:;, thL• development of manr species with bioluminescent propcrtico has becmm: incrcnsin~ly well docurnt·med. According to these srudics, biuluminc~c ~· n cc often arises l!:trly In omogcny. Tn date, however. very few studies have fix:used upon the early • .l lllt.lJ~t:ny d Aollhor.< <~ildr< : n.:s : 1Nnnlowt:>t Fhhcrk• Sckncc C•:nt cr.
    [Show full text]