Fishes Fishes Fishes Fishes

Total Page:16

File Type:pdf, Size:1020Kb

Fishes Fishes Fishes Fishes The Fishes of New Zealand Edited by Clive C Roberts, Andrew L Stewart and Carl D Struthers Published by Te Papa Press, November 2015 ISBN 9780994104168 RRP $250 The following images can be supplied for reproduction. Please include the book’s title, author, publisher, RRP and cover image. Images must include correct credit information. For further information and to request images contact Elizabeth Heritage, Te Papa Press publicist, phone: 022 652 3981, email: [email protected] Te Papa Press – Fishes of New Zealand Te Papa Press – Fishes of New Zealand Te Papa Press – Fishes of New Zealand Final Artwork – July 2015 Final Artwork – July 2015 Final Artwork – July 2015 Te Papa Press – Fishes of New Zealand Volume One Cover (18.5mm Spine) Volume Two Cover (33.5mm Spine) Volume Three Cover (33.5mm Spine) Final Artwork – July 2015 478.5 x 325mm (+20mm bleed) 493.5 x 325mm (+20mm bleed) 493.5 x 325mm (+20mm bleed) Volume Four Cover (35.5mm Spine) 495.5 x 325mm (+20mm bleed) THE THE THE THE THE THE THE THE FISHES FISHES FISHES FISHES FISHES FISHES FISHES FISHES Order Amphioxiformes – Lancelets Order Anguilliformes – Eels Order Aulopiformes – Lizardfishes (continued) Order Atheriniformes – Silversides 1 Family Epigonichthyidae – Lancelets 37 Family Anguillidae – Freshwater eels 82 Family Paralepididae – Barracudinas 125 Family Isonidae – Surf silversides Order Perciformes – Perch-like fishes 210 Family Cheimarrichthyidae – Torrentfish THE 38 Family Muraenidae – Moray eels 83 Family Anotopteridae – Daggertooths THE 164 Family Acropomatidae – Ocean bassesTHE 211 Family Creediidae – Tommyfishes Order Myxiniformes – Hagfishes 39 Family Synaphobranchidae – Cut-throat eels 84 Family Evermannellidae – Sabretooth fishes Order Beloniformes – Needlefishes 165 Family Polyprionidae – Wreckfishes 212 Family Percophidae – Opalfishes THE 2 Family Myxinidae – Hagfishes 40 Family Ophichthidae – Snake eels 166 Family Serranidae – Gropers and perches 213 Family Leptoscopidae – Stargazers Family Alepisauridae – Lancetfishes 85 126 Family Belonidae – Needlefishes OF 41 Family Derichthyidae – Longneck eels OF Family Grammistidae – Soapfishes Family Uranoscopidae – Armourhead 86 Family Omosudidae – Hammerjaw 127 Family Scomberesocidae – Sauries OF 167 214 Order Petromyzontiformes – Lampreys 42 Family Nemichthyidae – Snipe eels 87 Family Bathysauridae – Deepsea lizardfishes 128 Family Exocoetidae – Flyingfishes 168 Family Callanthiidae – Splendid perches stargazers OF 3 Family Geotriidae – Lampreys 43 Family Congridae – Conger eels 129 Family Hemiramphidae – Halfbeaks 169 Family Plesiopidae – Rockfishes 215 Family Tripterygiidae – Triplefins 44 Family Nettastomatidae – Duckbill eels Order Myctophiformes – Lanternfishes 170 Family Percidae – Freshwater perches 216 Family Clinidae – Weedfishes Order Chimaeriformes – Chimaeras 45 Family Serrivomeridae – Sawtooth eels 88 Family Neoscopelidae – Blackchins Order Cyprinodontiformes – Killifishes 171 Family Apogonidae – Cardinalfishes 217 Family Blenniidae – Blennies 4 Family Callorhinchidae – Elephantfishes 89 Family Myctophidae – Lanternfishes 130 Family Poeciliidae – Livebearers 172 Family Epigonidae – Deepsea cardinals 218 Family Gobiesocidae – Clingfishes NEW NEW NEW NEW 5 Family Chimaeridae – Shortnose chimaeras Order Saccopharyngiformes – Sackpharynx fishes NEW 173 Family Howellidae – Pelagic basslets 219 Family Callionymidae – Dragonets 6 FISHES Family Rhinochimaeridae – Longnose 46 Family Cyematidae – Bobtail snipe eels 174 Family Priacanthidae – Bigeyes 220 Family Draconettidae – Deepsea dragonets NEW OrderFISHES Lampriformes – Opahs Order Stephanoberyciformes – Pricklefishes FISHES chimaeras 47 Family Saccopharyngidae – Whiptail gulpers 90 Family Veliferidae – Velifers 131 Family Melamphaidae – Bigscales 175 Family Malacanthidae – Tilefishes 221 Family Eleotridae – Bullies FISHES OF NEW ZEALAND48 Family Eurypharyngidae – Pelican eel 91 Family LampridaeOF – Opahs NEW ZEALAND132 Family Stephanoberycidae – Pricklefishes 176 Family EcheneidaeOF – Remoras NEW ZEALAND222 Family Gobiidae – Gobies Order Heterodontiformes – Horn sharks 92 Family Lophotidae – Crestfishes 133 Family Rondeletiidae – Redmouth 177 Family Kuhliidae – Flagtails 223 Family Microdesmidae – Dart gobies OF NEW ZEALAND 7 Family Heterodontidae – Horn sharks Order Clupeiformes – Herrings 93 Family Trachipteridae – Dealfishes whalefishes 178 Family Coryphaenidae – Dolphinfishes 224 Family Ephippidae – Spadefishes VOLUME ONE49 Family Engraulidae – Anchovies 94 Family Regalecidae – Oarfishes 134 Family Barbourisiidae – Red whalefish 179 Family Carangidae – Trevallies 225 Family Luvaridae – Luvar Family Clupeidae – Sardines VOLUME TWO Order Lamniformes – Mackerel sharks 50 135 Family Cetomimidae – Flabby whalefishes 180 Family Bramidae – Pomfrets VOLUME THREE226 Family Zanclidae – Moorish idol INTRODUCTION AND VOLUME FOUR ZEALAND 8 Family Odontaspididae – Sandtiger sharks SYSTEMATIC ACCOUNTS 181 Family Caristiidae – Manefishes 227 Family Acanthuridae – Surgeonfishes ZEALAND Order Polymixiiformes – Beardfishes SYSTEMATIC ACCOUNTS ZEALAND 9 Family MitsukurinidaeSUPPLEMENTARY – Goblin shark Order MATTER Gonorynchiformes – Sandfishes PAGES 1–576 182 Family Emmelichthyidae – Bonnetmouths 228 Family Scombrolabracidae – Black mackerel SYSTEMATIC ACCOUNTS 95 Family Polymixiidae – Beardfishes Order Beryciformes – Alfonsinos and squirrelfishes ZEALAND 10 Family Pseudocarchariidae – Crocodile shark 51 Family Gonorynchidae – Sandfishes PAGES 577–1152 136 Family Anoplogastridae – Fangtooths 183 Family Lutjanidae – Tropical snappers 229 Family Sphyraenidae – Barracudas PAGES 1153–1748 11 Family Alopiidae – Thresher sharks Order Ophidiiformes – Cuskeels 137 Family Diretmidae – Discfishes 184 Family Sparidae – Seabreams 230 Family Gempylidae – Gemfishes 12 Family Cetorhinidae – Basking shark Order Cypriniformes – Carps 185 Family Mullidae – Goatfishes 231 Family Trichiuridae – Scabbardfishes 96 Family Carapidae – Messmates 138 Family Monocentridae – Pineapplefishes 13 Family Lamnidae – MackerelEdited sharks by Clive D Roberts,52 Family Cyprinidae – Carps Edited by Clive D Roberts, 186 Family Pempheridae – Bullseyes 232 Family Scombridae – Mackerels and tunas 97 Family Ophidiidae – Cuskeels 139 Family Trachichthyidae – Roughies Edited by Clive D Roberts, Andrew L Stewart, and Carl D Struthers 187 Family Chaetodontidae – Butterflyfishes 233 Family Istiophoridae – Billfishes Edited by Clive D Roberts, 98 Family Bythitidae – Brotulas Andrew L Stewart, and Carl140 DFamily Struthers Berycidae – Alfonsinos Order Carcharhiniformes – Ground sharks Order Siluriformes – Catfishes 188 Family Pomacanthidae Andrew – Angelfishes L Stewart, and Carl234 D Family Struthers Xiphiidae – Swordfish 99 Family Aphyonidae – Aphyonids 141 Family Holocentridae – Squirrelfishes Andrew L Stewart, and Carl D Struthers 14 Family Scyliorhinidae – Catsharks 53 Family Ictaluridae – North American freshwater 189 Family Pentacerotidae – Boarfishes 235 Family Centrolophidae – Warehous 15 Family Pseudotriakidae – False catsharks catfishes 190 Family Kyphosidae – Drummers 236 Family Nomeidae – Cubeheads Order Gadiformes – Cods Order Zeiformes – Dories 16 Family Triakidae – Houndsharks and 191 Family Girellidae – Nibblers 237 Family Ariommatidae – Ariommids 100 Family Muraenolepididae – Moray cods 142 Family Zeidae – Dories smooth-hounds Order Argentiniformes – Marine smelts 192 Family Scorpididae – Sweeps 238 Family Tetragonuridae – Squaretails 101 Family Bregmacerotidae – Codlets Family Grammicolepididae – Tinselfishes 17 Family Carcharhinidae – Requiem sharks 54 Family Argentinidae – Silversides 143 193 Family Microcanthidae – Stripeys Family Euclichthyidae – Eucla cods Family Parazenidae – Slender dories 18 Family Sphyrnidae – Hammerhead sharks 55 Family Opisthoproctidae – Spookfishes 102 144 194 Family Arripidae – Kahawai Order Pleuronectiformes – Flatfishes 56 Family Microstomatidae – White smelts 103 Family Macrouridae – Rattails 145 Family Cyttidae – Cyttid dories 195 Family Oplegnathidae – Knifejaws 239 Family Bothidae – Lefteye flounders Order Orectolobiformes – Carpet sharks 57 Family Bathylagidae – Deepsea smelts 104 Family Bathygadidae – Codhead rattails 146 Family Zeniontidae – Armoureye dories 196 Family Cirrhitidae – Hawkfishes 240 Family Achiropsettidae – Finless flounders 19 Family Rhincodontidae – Whale shark 58 Family Platytroctidae – Tubeshoulders 105 Family Macrouroididae – Balloonhead rattails 147 Family Oreosomatidae – Oreo dories 197 Family Chironemidae – Kelpfishes 241 Family Rhombosoleidae – Southern righteye 59 Family Alepocephalidae – Slickheads 106 Family Trachyrincidae – Rough rattails 198 Family Aplodactylidae – Marblefishes flounders Order Hexanchiformes – Sevengill sharks and 107 Family Moridae – Morid cods Order Gasterosteiformes – Pipefishes and seahorses 199 Family Cheilodactylidae – Moki and tarakihi 242 Family Soleidae – True soles sixgill sharks Order Salmoniformes – Trouts, freshwater smelts, 108 Family Melanonidae – Pelagic cods 148 Family Syngnathidae – Pipefishes and 200 Family Latridae – Trumpeters 243 Family Cynoglossidae – Tonguefishes 20 Family Chlamydoselachidae Frill sharks and galaxiids 109 Family Merlucciidae – Hakes seahorses 201 Family Cepolidae – Bandfishes 110 Family Lotidae – Rocklings 149 Family Aulostomidae – Trumpetfishes 202 Family Labridae – Wrasses Order Tetraodontiformes – Puffers V 21 Family Hexanchidae Sevengill sharks and 60 Family Retropinnidae – Southern smelts V 111 Family Gadidae – True cods 150 Family Fistulariidae
Recommended publications
  • Order BERYCIFORMES ANOPLOGASTRIDAE Anoplogaster
    click for previous page 2210 Bony Fishes Order BERYCIFORMES ANOPLOGASTRIDAE Fangtooths by J.R. Paxton iagnostic characters: Small (to 16 cm) Dberyciform fishes, body short, deep, and compressed. Head large, steep; deep mu- cous cavities on top of head separated by serrated crests; very large temporal and pre- opercular spines and smaller orbital (frontal) spine in juveniles of one species, all disap- pearing with age. Eyes smaller than snout length in adults (but larger than snout length in juveniles). Mouth very large, jaws extending far behind eye in adults; one supramaxilla. Teeth as large fangs in pre- maxilla and dentary; vomer and palatine toothless. Gill rakers as gill teeth in adults (elongate, lath-like in juveniles). No fin spines; dorsal fin long based, roughly in middle of body, with 16 to 20 rays; anal fin short-based, far posterior, with 7 to 9 rays; pelvic fin abdominal in juveniles, becoming subthoracic with age, with 7 rays; pectoral fin with 13 to 16 rays. Scales small, non-overlap- ping, spinose, cup-shaped in adults; lateral line an open groove partly covered by scales. No light organs. Total vertebrae 25 to 28. Colour: brown-black in adults. Habitat, biology, and fisheries: Meso- and bathypelagic. Distinctive caulolepis juvenile stage, with greatly enlarged head spines in one species. Feeding mode as carnivores on crustaceans as juveniles and on fishes as adults. Rare deepsea fishes of no commercial importance. Remarks: One genus with 2 species throughout the world ocean in tropical and temperate latitudes. The family was revised by Kotlyar (1986). Similar families occurring in the area Diretmidae: No fangs, jaw teeth small, in bands; anal fin with 18 to 24 rays.
    [Show full text]
  • Percomorph Phylogeny: a Survey of Acanthomorphs and a New Proposal
    BULLETIN OF MARINE SCIENCE, 52(1): 554-626, 1993 PERCOMORPH PHYLOGENY: A SURVEY OF ACANTHOMORPHS AND A NEW PROPOSAL G. David Johnson and Colin Patterson ABSTRACT The interrelationships of acanthomorph fishes are reviewed. We recognize seven mono- phyletic terminal taxa among acanthomorphs: Lampridiformes, Polymixiiformes, Paracan- thopterygii, Stephanoberyciformes, Beryciformes, Zeiformes, and a new taxon named Smeg- mamorpha. The Percomorpha, as currently constituted, are polyphyletic, and the Perciformes are probably paraphyletic. The smegmamorphs comprise five subgroups: Synbranchiformes (Synbranchoidei and Mastacembeloidei), Mugilomorpha (Mugiloidei), Elassomatidae (Elas- soma), Gasterosteiformes, and Atherinomorpha. Monophyly of Lampridiformes is justified elsewhere; we have found no new characters to substantiate the monophyly of Polymixi- iformes (which is not in doubt) or Paracanthopterygii. Stephanoberyciformes uniquely share a modification of the extrascapular, and Beryciformes a modification of the anterior part of the supraorbital and infraorbital sensory canals, here named Jakubowski's organ. Our Zei- formes excludes the Caproidae, and characters are proposed to justify the monophyly of the group in that restricted sense. The Smegmamorpha are thought to be monophyletic principally because of the configuration of the first vertebra and its intermuscular bone. Within the Smegmamorpha, the Atherinomorpha and Mugilomorpha are shown to be monophyletic elsewhere. Our Gasterosteiformes includes the syngnathoids and the Pegasiformes
    [Show full text]
  • 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]
  • Biodiversity of Arctic Marine Fishes: Taxonomy and Zoogeography
    Mar Biodiv DOI 10.1007/s12526-010-0070-z ARCTIC OCEAN DIVERSITY SYNTHESIS Biodiversity of arctic marine fishes: taxonomy and zoogeography Catherine W. Mecklenburg & Peter Rask Møller & Dirk Steinke Received: 3 June 2010 /Revised: 23 September 2010 /Accepted: 1 November 2010 # Senckenberg, Gesellschaft für Naturforschung and Springer 2010 Abstract Taxonomic and distributional information on each Six families in Cottoidei with 72 species and five in fish species found in arctic marine waters is reviewed, and a Zoarcoidei with 55 species account for more than half list of families and species with commentary on distributional (52.5%) the species. This study produced CO1 sequences for records is presented. The list incorporates results from 106 of the 242 species. Sequence variability in the barcode examination of museum collections of arctic marine fishes region permits discrimination of all species. The average dating back to the 1830s. It also incorporates results from sequence variation within species was 0.3% (range 0–3.5%), DNA barcoding, used to complement morphological charac- while the average genetic distance between congeners was ters in evaluating problematic taxa and to assist in identifica- 4.7% (range 3.7–13.3%). The CO1 sequences support tion of specimens collected in recent expeditions. Barcoding taxonomic separation of some species, such as Osmerus results are depicted in a neighbor-joining tree of 880 CO1 dentex and O. mordax and Liparis bathyarcticus and L. (cytochrome c oxidase 1 gene) sequences distributed among gibbus; and synonymy of others, like Myoxocephalus 165 species from the arctic region and adjacent waters, and verrucosus in M. scorpius and Gymnelus knipowitschi in discussed in the family reviews.
    [Show full text]
  • 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.
    [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]
  • Phylogeny and Fitness of Vibrio Fischeri from the Light Organs of Euprymna Scolopes in Two Oahu, Hawaii Populations
    The ISME Journal (2011), 1–11 & 2011 International Society for Microbial Ecology All rights reserved 1751-7362/11 www.nature.com/ismej ORIGINAL ARTICLE Phylogeny and fitness of Vibrio fischeri from the light organs of Euprymna scolopes in two Oahu, Hawaii populations Michael S Wollenberg and Edward G Ruby Department of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI, USA The evolutionary relationship among Vibrio fischeri isolates obtained from the light organs of Euprymna scolopes collected around Oahu, Hawaii, were examined in this study. Phylogenetic reconstructions based on a concatenation of fragments of four housekeeping loci (recA, mdh, katA, pyrC) identified one monophyletic group (‘Group-A’) of V. fischeri from Oahu. Group-A V. fischeri strains could also be identified by a single DNA fingerprint type. V. fischeri strains with this fingerprint type had been observed to be at a significantly higher abundance than other strains in the light organs of adult squid collected from Maunalua Bay, Oahu, in 2005. We hypothesized that these previous observations might be related to a growth/survival advantage of the Group-A strains in the Maunalua Bay environments. Competition experiments between Group-A strains and non- Group-A strains demonstrated an advantage of the former in colonizing juvenile Maunalua Bay hosts. Growth and survival assays in Maunalua Bay seawater microcosms revealed a reduced fitness of Group-A strains relative to non-Group-A strains. From these results, we hypothesize that there may exist trade-offs between growth in the light organ and in seawater environments for local V. fischeri strains from Oahu.
    [Show full text]
  • Fishes-Of-The-Salish-Sea-Pp18.Pdf
    NOAA Professional Paper NMFS 18 Fishes of the Salish Sea: a compilation and distributional analysis Theodore W. Pietsch James W. Orr September 2015 U.S. Department of Commerce NOAA Professional Penny Pritzker Secretary of Commerce Papers NMFS National Oceanic and Atmospheric Administration Kathryn D. Sullivan Scientifi c Editor Administrator Richard Langton National Marine Fisheries Service National Marine Northeast Fisheries Science Center Fisheries Service Maine Field Station Eileen Sobeck 17 Godfrey Drive, Suite 1 Assistant Administrator Orono, Maine 04473 for Fisheries Associate Editor Kathryn Dennis National Marine Fisheries Service Offi ce of Science and Technology Fisheries Research and Monitoring Division 1845 Wasp Blvd., Bldg. 178 Honolulu, Hawaii 96818 Managing Editor Shelley Arenas National Marine Fisheries Service Scientifi c Publications Offi ce 7600 Sand Point Way NE Seattle, Washington 98115 Editorial Committee Ann C. Matarese National Marine Fisheries Service James W. Orr National Marine Fisheries Service - The NOAA Professional Paper NMFS (ISSN 1931-4590) series is published by the Scientifi c Publications Offi ce, National Marine Fisheries Service, The NOAA Professional Paper NMFS series carries peer-reviewed, lengthy original NOAA, 7600 Sand Point Way NE, research reports, taxonomic keys, species synopses, fl ora and fauna studies, and data- Seattle, WA 98115. intensive reports on investigations in fi shery science, engineering, and economics. The Secretary of Commerce has Copies of the NOAA Professional Paper NMFS series are available free in limited determined that the publication of numbers to government agencies, both federal and state. They are also available in this series is necessary in the transac- exchange for other scientifi c and technical publications in the marine sciences.
    [Show full text]
  • Evolution and Ecology in Widespread Acoustic Signaling Behavior Across Fishes
    bioRxiv preprint doi: https://doi.org/10.1101/2020.09.14.296335; this version posted September 14, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 Evolution and Ecology in Widespread Acoustic Signaling Behavior Across Fishes 2 Aaron N. Rice1*, Stacy C. Farina2, Andrea J. Makowski3, Ingrid M. Kaatz4, Philip S. Lobel5, 3 William E. Bemis6, Andrew H. Bass3* 4 5 1. Center for Conservation Bioacoustics, Cornell Lab of Ornithology, Cornell University, 159 6 Sapsucker Woods Road, Ithaca, NY, USA 7 2. Department of Biology, Howard University, 415 College St NW, Washington, DC, USA 8 3. Department of Neurobiology and Behavior, Cornell University, 215 Tower Road, Ithaca, NY 9 USA 10 4. Stamford, CT, USA 11 5. Department of Biology, Boston University, 5 Cummington Street, Boston, MA, USA 12 6. Department of Ecology and Evolutionary Biology and Cornell University Museum of 13 Vertebrates, Cornell University, 215 Tower Road, Ithaca, NY, USA 14 15 ORCID Numbers: 16 ANR: 0000-0002-8598-9705 17 SCF: 0000-0003-2479-1268 18 WEB: 0000-0002-5669-2793 19 AHB: 0000-0002-0182-6715 20 21 *Authors for Correspondence 22 ANR: [email protected]; AHB: [email protected] 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.09.14.296335; this version posted September 14, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.
    [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]
  • The Tree of Life and a New Classification of Bony Fishes
    The Tree of Life and a New Classification of Bony Fishes April 18, 2013 · Tree of Life Ricardo Betancur-R.1, Richard E. Broughton2, Edward O. Wiley3, Kent Carpenter4, J. Andrés López5, Chenhong Li 6, Nancy I. Holcroft7, Dahiana Arcila1, Millicent Sanciangco4, James C Cureton II2, Feifei Zhang2, Thaddaeus Buser, Matthew A. Campbell5, Jesus A Ballesteros1, Adela Roa-Varon8, Stuart Willis9, W. Calvin Borden10, Thaine Rowley11, Paulette C. Reneau12, Daniel J. Hough2, Guoqing Lu13, Terry Grande10, Gloria Arratia3, Guillermo Ortí1 1 The George Washington University, 2 University of Oklahoma, 3 University of Kansas, 4 Old Dominion University, 5 University of Alaska Fairbanks, 6 Shanghai Ocean University, 7 Johnson County Community College, 8 George Washington University, 9 University of Nebraska-Lincoln, 10 Loyola University Chicago, 11 University of Nebraska- Omaha, 12 Florida A&M University, 13 University of Nebraska at Omaha Betancur-R. R, Broughton RE, Wiley EO, Carpenter K, López JA, Li C, Holcroft NI, Arcila D, Sanciangco M, Cureton II JC, Zhang F, Buser T, Campbell MA, Ballesteros JA, Roa-Varon A, Willis S, Borden WC, Rowley T, Reneau PC, Hough DJ, Lu G, Grande T, Arratia G, Ortí G. The Tree of Life and a New Classification of Bony Fishes. PLOS Currents Tree of Life. 2013 Apr 18 [last modified: 2013 Apr 23]. Edition 1. doi: 10.1371/currents.tol.53ba26640df0ccaee75bb165c8c26288. Abstract The tree of life of fishes is in a state of flux because we still lack a comprehensive phylogeny that includes all major groups. The situation is most critical for a large clade of spiny-finned fishes, traditionally referred to as percomorphs, whose uncertain relationships have plagued ichthyologists for over a century.
    [Show full text]
  • Convergence in Diet and Morphology in Marine and Freshwater Cottoid Fishes Darby Finnegan1,2
    Convergence in Diet and Morphology in Marine and Freshwater Cottoid Fishes Darby Finnegan1,2 Blinks-NSF REU-BEACON 2017 Summer 2017 1Friday Harbor Laboratories, University of Washington, Friday Harbor, WA 98250 2Department of Biology, Western Washington University, Bellingham, WA 98225 Contact information: Darby Finnegan Department of Biology Western Washington University 516 High Street Bellingham, WA 98225 [email protected] Keywords: Cottoid, marine-freshwater transitions, functional morphology, ecomorphology, adaptive optima, species diversification, adaptive radiation Abstract Habitat transitions provide opportunities for drastic changes in ecology, morphology, and behavior of organisms. The goal of this study is to determine whether the numerous evolutionary transitions from marine to freshwaters have altered the pattern and pace of morphological and lineage diversification within the sculpins (Cottoidea). The broad global distribution and wide-ranging ecology of sculpins make them an ideal study system in which to analyze marine invasions in northern latitudes. The sheer diversity of sculpins in isolated systems like Lake Baikal has led some to suggest these fishes (particularly Cottus) underwent an adaptive radiation upon their invasion of freshwaters in north Asia and Europe. Marine sculpins appear to be more diverse than freshwater sculpins, and while cottoids show signs of explosive radiation early in their evolutionary history, our study shows that unequal patterns of clade disparity among these lineages has led to constant rates of morphological and lineage diversification. Feeding morphology traits are highly conserved in cottoids, with both marine and freshwater species displaying similar morphologies despite widely-varying diets. While convergence in feeding morphology and dietary ecology is widespread in freshwater and marine cottoids, some specialist taxa, including planktivores and piscivores, show notable departures from the ancestral sculpin body plan.
    [Show full text]