Order BERYCIFORMES ANOPLOGASTRIDAE Anoplogaster
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Zoology Marine Ornamental Fish Biodiversity of West Bengal ABSTRACT
Research Paper Volume : 4 | Issue : 8 | Aug 2015 • ISSN No 2277 - 8179 Zoology Marine Ornamental Fish Biodiversity of KEYWORDS : Marine fish, ornamental, West Bengal diversity, West Bengal. Principal Scientist and Scientist-in-Charge, ICAR-Central Institute of Fisheries Education, Dr. B. K. Mahapatra Salt Lake City, Kolkata-700091, India Director and Vice-Chancellor, ICAR-Central Institute of Fisheries Education, Versova, Dr. W. S. Lakra Mumbai- 400 061, India ABSTRACT The State of West Bengal, India endowed with 158 km coast line for marine water resources with inshore, up-shore areas and continental shelf of Bay of Bengal form an important fishery resource and also possesses a rich wealth of indigenous marine ornamental fishes.The present study recorded a total of 113 marine ornamental fish species, belonging to 75 genera under 45 families and 10 orders.Order Perciformes is represented by a maximum of 26 families having 79 species under 49 genera followed by Tetraodontiformes (5 family; 9 genus and 10 species), Scorpaeniformes (2 family; 3 genus and 6 species), Anguilliformes (2 family; 3 genus and 4 species), Syngnathiformes (2 family; 3 genus and 3 species), Pleuronectiformes (2 family; 2 genus and 4 species), Siluriformes (2 family; 2 genus and 3 species), Beloniformes (2 family; 2 genus and 2 species), Lophiformes (1 family; 1 genus and 1 species), Beryciformes(1 family; 1 genus and 1 species). Introduction Table 1: List of Marine ornamental fishes of West Bengal Ornamental fishery, which started centuries back as a hobby, ORDER 1: PERCIFORMES has now started taking the shape of a multi-billion dollar in- dustry. -
Order BERYCIFORMES ANOPLOGASTRIDAE Fangtooths (Ogrefish) by J.A
click for previous page 1178 Bony Fishes Order BERYCIFORMES ANOPLOGASTRIDAE Fangtooths (ogrefish) by J.A. Moore, Florida Atlantic University, USA iagnostic characters: Small (to about 160 mm standard length) beryciform fishes.Body short, deep, and Dcompressed, tapering to narrow peduncle. Head large (1/3 standard length). Eye smaller than snout length in adults, but larger than snout length in juveniles. Mouth very large and oblique, jaws extend be- hind eye in adults; 1 supramaxilla. Bands of villiform teeth in juveniles are replaced with large fangs on dentary and premaxilla in adults; vomer and palatines toothless. Deep sensory canals separated by ser- rated ridges; very large parietal and preopercular spines in juveniles of one species, all disappearing with age. Gill rakers as clusters of teeth on gill arch in adults (lath-like in juveniles). No true fin spines; single, long-based dorsal fin with 16 to 20 rays; anal fin very short-based with 7 to 9 soft rays; caudal fin emarginate; pectoral fins with 13 to 16 soft rays; pelvic fins with 7 soft rays. Scales small, non-overlapping, spinose, goblet-shaped in adults; lateral line an open groove partially bridged by scales; no enlarged ventral keel scutes. Colour: entirely dark brown or black in adults. Habitat, biology, and fisheries: Meso- to bathypelagic, at depths of 75 to 5 000 m. Carnivores, with juveniles feeding on mainly crustaceans and adults mainly on fishes. May sometimes swim in small groups. Uncommon deep-sea fishes of no commercial importance. Remarks: The family was revised recently by Kotlyar (1986) and contains 1 genus with 2 species throughout the tropical and temperate latitudes. -
Hoplostethus Atlanticus Fisheries Relating to the South Pacific Regional Fishery Management Organisation
SP-07-SWG-INF-09 Chile 13 May 2009 Information describing orange roughy Hoplostethus atlanticus fisheries relating to the South Pacific Regional Fishery Management Organisation WORKING DRAFT 04 MAY 2007 1. Overview ................................................................................................................ 2 2. Taxonomy .............................................................................................................. 3 2.1 Phylum ............................................................................................................. 3 2.2 Class ................................................................................................................. 3 2.3 Order ................................................................................................................ 3 2.4 Family .............................................................................................................. 3 2.5 Genus and species ............................................................................................ 3 2.6 Scientific synonyms ......................................................................................... 3 2.7 Common names ............................................................................................... 3 2.8 Molecular (DNA or biochemical) bar coding .................................................. 3 3. Species characteristics ........................................................................................... 4 3.1 Global distribution and depth range -
§4-71-6.5 LIST of CONDITIONALLY APPROVED ANIMALS November
§4-71-6.5 LIST OF CONDITIONALLY APPROVED ANIMALS November 28, 2006 SCIENTIFIC NAME COMMON NAME INVERTEBRATES PHYLUM Annelida CLASS Oligochaeta ORDER Plesiopora FAMILY Tubificidae Tubifex (all species in genus) worm, tubifex PHYLUM Arthropoda CLASS Crustacea ORDER Anostraca FAMILY Artemiidae Artemia (all species in genus) shrimp, brine ORDER Cladocera FAMILY Daphnidae Daphnia (all species in genus) flea, water ORDER Decapoda FAMILY Atelecyclidae Erimacrus isenbeckii crab, horsehair FAMILY Cancridae Cancer antennarius crab, California rock Cancer anthonyi crab, yellowstone Cancer borealis crab, Jonah Cancer magister crab, dungeness Cancer productus crab, rock (red) FAMILY Geryonidae Geryon affinis crab, golden FAMILY Lithodidae Paralithodes camtschatica crab, Alaskan king FAMILY Majidae Chionocetes bairdi crab, snow Chionocetes opilio crab, snow 1 CONDITIONAL ANIMAL LIST §4-71-6.5 SCIENTIFIC NAME COMMON NAME Chionocetes tanneri crab, snow FAMILY Nephropidae Homarus (all species in genus) lobster, true FAMILY Palaemonidae Macrobrachium lar shrimp, freshwater Macrobrachium rosenbergi prawn, giant long-legged FAMILY Palinuridae Jasus (all species in genus) crayfish, saltwater; lobster Panulirus argus lobster, Atlantic spiny Panulirus longipes femoristriga crayfish, saltwater Panulirus pencillatus lobster, spiny FAMILY Portunidae Callinectes sapidus crab, blue Scylla serrata crab, Samoan; serrate, swimming FAMILY Raninidae Ranina ranina crab, spanner; red frog, Hawaiian CLASS Insecta ORDER Coleoptera FAMILY Tenebrionidae Tenebrio molitor mealworm, -
New Insights on the Sister Lineage of Percomorph Fishes with an Anchored Hybrid Enrichment Dataset
Molecular Phylogenetics and Evolution 110 (2017) 27–38 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev New insights on the sister lineage of percomorph fishes with an anchored hybrid enrichment dataset ⇑ Alex Dornburg a, , Jeffrey P. Townsend b,c,d, Willa Brooks a, Elizabeth Spriggs b, Ron I. Eytan e, Jon A. Moore f,g, Peter C. Wainwright h, Alan Lemmon i, Emily Moriarty Lemmon j, Thomas J. Near b,k a North Carolina Museum of Natural Sciences, Raleigh, NC, USA b Department of Ecology & Evolutionary Biology and Peabody Museum of Natural History, Yale University, New Haven, CT 06520, USA c Program in Computational Biology and Bioinformatics, Yale University, New Haven, CT 06520, USA d Department of Biostatistics, Yale University, New Haven, CT 06510, USA e Marine Biology Department, Texas A&M University at Galveston, Galveston, TX 77554, USA f Florida Atlantic University, Wilkes Honors College, Jupiter, FL 33458, USA g Florida Atlantic University, Harbor Branch Oceanographic Institution, Fort Pierce, FL 34946, USA h Department of Evolution & Ecology, University of California, Davis, CA 95616, USA i Department of Scientific Computing, Florida State University, 400 Dirac Science Library, Tallahassee, FL 32306, USA j Department of Biological Science, Florida State University, 319 Stadium Drive, Tallahassee, FL 32306, USA k Peabody Museum of Natural History, Yale University, New Haven, CT 06520, USA article info abstract Article history: Percomorph fishes represent over 17,100 species, including several model organisms and species of eco- Received 12 April 2016 nomic importance. Despite continuous advances in the resolution of the percomorph Tree of Life, resolu- Revised 22 February 2017 tion of the sister lineage to Percomorpha remains inconsistent but restricted to a small number of Accepted 25 February 2017 candidate lineages. -
Jolanta KEMPTER*, Maciej KIEŁPIŃSKI, Remigiusz PANICZ, and Sławomir KESZKA
ACTA ICHTHYOLOGICA ET PISCATORIA (2016) 46 (4): 287–291 DOI: 10.3750/AIP2016.46.4.02 MICROSATELLITE DNA-BASED GENETIC TRACEABILITY OF TWO POPULATIONS OF SPLENDID ALFONSINO, BERYX SPLENDENS (ACTINOPTERYGII: BERYCIFORMES: BERYCIDAE)—PROJECT CELFISH—PART 2 Jolanta KEMPTER*, Maciej KIEŁPIŃSKI, Remigiusz PANICZ, and Sławomir KESZKA Division of Aquaculture, West Pomeranian University of Technology, Szczecin, Kazimierza Krolewicza 4, 71-550 Szczecin, Poland Kempter J., Kiełpinski M., Panicz R., Keszka S. 2016. Microsatellite DNA-based genetic traceability of two populations of splendid alfonsino, Beryx splendens (Actinopterygii: Beryciformes: Berycidae)— Project CELFISH—Part 2. Acta Ichthyol. Piscat. 46 (4): 287–291. Background. The study is a contribution to Project CELFISH which involves genetic identifi cation of populations of fi sh species presenting a particular economic importance or having a potential to be used in the so-called commercial substitutions. The EU fi sh trade has been showing a distinct trend of more and more fi sh species previously unknown to consumers being placed on the market. Molecular assays have become the only way with which to verify the reliability of exporters. This paper is aimed at pinpointing genetic markers with which to label and differentiate between two populations of splendid alfonsino, Beryx splendens Lowe, 1834, a species highly attractive to consumers in Asia and Oceania due to the meat taste and low fat content. Material and methods. DNA was isolated from fragments of fi ns collected at local markets in Japan (MJ) (n = 10) and New Zealand (MNZ) (n = 18). The rhodopsin gene (RH1) fragment and 16 microsatellite DNA fragments (SSR) were analysed in all the individuals. -
Larvae and Juveniles of the Deepsea “Whalefishes”
© Copyright Australian Museum, 2001 Records of the Australian Museum (2001) Vol. 53: 407–425. ISSN 0067-1975 Larvae and Juveniles of the Deepsea “Whalefishes” Barbourisia and Rondeletia (Stephanoberyciformes: Barbourisiidae, Rondeletiidae), with Comments on Family Relationships JOHN R. PAXTON,1 G. DAVID JOHNSON2 AND THOMAS TRNSKI1 1 Fish Section, Australian Museum, 6 College Street, Sydney NSW 2010, Australia [email protected] [email protected] 2 Fish Division, National Museum of Natural History, Smithsonian Institution, Washington, D.C. 20560, U.S.A. [email protected] ABSTRACT. Larvae of the deepsea “whalefishes” Barbourisia rufa (11: 3.7–14.1 mm nl/sl) and Rondeletia spp. (9: 3.5–9.7 mm sl) occur at least in the upper 200 m of the open ocean, with some specimens taken in the upper 20 m. Larvae of both families are highly precocious, with identifiable features in each by 3.7 mm. Larval Barbourisia have an elongate fourth pelvic ray with dark pigment basally, notochord flexion occurs between 6.5 and 7.5 mm sl, and by 7.5 mm sl the body is covered with small, non- imbricate scales with a central spine typical of the adult. In Rondeletia notochord flexion occurs at about 3.5 mm sl and the elongate pelvic rays 2–4 are the most strongly pigmented part of the larvae. Cycloid scales (here reported in the family for the first time) are developing by 7 mm; these scales later migrate to form a layer directly over the muscles underneath the dermis. By 7 mm sl there is a unique organ, here termed Tominaga’s organ, separate from and below the nasal rosette, developing anterior to the eye. -
Diverse Deep-Sea Anglerfishes Share a Genetically Reduced Luminous
RESEARCH ARTICLE Diverse deep-sea anglerfishes share a genetically reduced luminous symbiont that is acquired from the environment Lydia J Baker1*, Lindsay L Freed2, Cole G Easson2,3, Jose V Lopez2, Dante´ Fenolio4, Tracey T Sutton2, Spencer V Nyholm5, Tory A Hendry1* 1Department of Microbiology, Cornell University, New York, United States; 2Halmos College of Natural Sciences and Oceanography, Nova Southeastern University, Fort Lauderdale, United States; 3Department of Biology, Middle Tennessee State University, Murfreesboro, United States; 4Center for Conservation and Research, San Antonio Zoo, San Antonio, United States; 5Department of Molecular and Cell Biology, University of Connecticut, Storrs, United States Abstract Deep-sea anglerfishes are relatively abundant and diverse, but their luminescent bacterial symbionts remain enigmatic. The genomes of two symbiont species have qualities common to vertically transmitted, host-dependent bacteria. However, a number of traits suggest that these symbionts may be environmentally acquired. To determine how anglerfish symbionts are transmitted, we analyzed bacteria-host codivergence across six diverse anglerfish genera. Most of the anglerfish species surveyed shared a common species of symbiont. Only one other symbiont species was found, which had a specific relationship with one anglerfish species, Cryptopsaras couesii. Host and symbiont phylogenies lacked congruence, and there was no statistical support for codivergence broadly. We also recovered symbiont-specific gene sequences from water collected near hosts, suggesting environmental persistence of symbionts. Based on these results we conclude that diverse anglerfishes share symbionts that are acquired from the environment, and *For correspondence: that these bacteria have undergone extreme genome reduction although they are not vertically [email protected] (LJB); transmitted. -
How Much Longer Will It Take?
How much longer will it take? A ten-year review of the implementation of United Nations General Assembly resolutions 61/105, 64/72 and 66/68 on the management of bottom fisheries in areas beyond national jurisdiction FULL REPORT – AUGUST 2016 DAVID SHALE/NATURE PICTURE LIBRARAY SHALE/NATURE DAVID Leiopathes sp., a deepwater black coral, has lifespans in excess of 4,200 years (Roark et al., 2009*), making it one of the oldest living organism on Earth. Specimen was located off the coast of Oahu, Hawaii, in ~400 m water depth. * Roark, E.B., Guilderson, T.P., Dunbar, R.B., Fallon, S.J., and Mucciarone, D.A., 2009. Extreme longevity in proteinaceous deep-sea corals. Proceedings of the National Academy of Sciences, 106: 520– 5208, doi: 10.1073/pnas.0810875106. © HAWAII UNDERSEA RESEARCH LABORATORY, TERRY KERBY AND MAXIMILIAN CREMER Contents Executive summary 03 1.0 Introduction 09 2.0 North Atlantic 10 2.1 Northeast Atlantic 10 2..2 Northwest Atlantic 21 3.0 South Atlantic 33 3.1 Southeast Atlantic 33 3.2 Southwest Atlantic and other non-RFMO areas 39 4.0 North Pacific 42 Citation: 5.0 South Pacific 49 Gianni, M., Fuller, S.D., Currie, D.E.J., Schleit, 6.0 Indian Ocean 60 K., Goldsworthy, L., Pike, B., Weeber, B., 7.0 Southern Ocean 66 Owen, S., Friedman, A. How much longer will it take? A ten-year 8.0. Mediterranean Sea 71 review of the implementation of United Annex 1. Acronyms 73 Nations General Assembly resolutions Annex 2. History of the UNGA negotiations 73 61/105, 64/72 and 66/68 on the management Annex 3. -
Updated Checklist of Marine Fishes (Chordata: Craniata) from Portugal and the Proposed Extension of the Portuguese Continental Shelf
European Journal of Taxonomy 73: 1-73 ISSN 2118-9773 http://dx.doi.org/10.5852/ejt.2014.73 www.europeanjournaloftaxonomy.eu 2014 · Carneiro M. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph urn:lsid:zoobank.org:pub:9A5F217D-8E7B-448A-9CAB-2CCC9CC6F857 Updated checklist of marine fishes (Chordata: Craniata) from Portugal and the proposed extension of the Portuguese continental shelf Miguel CARNEIRO1,5, Rogélia MARTINS2,6, Monica LANDI*,3,7 & Filipe O. COSTA4,8 1,2 DIV-RP (Modelling and Management Fishery Resources Division), Instituto Português do Mar e da Atmosfera, Av. Brasilia 1449-006 Lisboa, Portugal. E-mail: [email protected], [email protected] 3,4 CBMA (Centre of Molecular and Environmental Biology), Department of Biology, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal. E-mail: [email protected], [email protected] * corresponding author: [email protected] 5 urn:lsid:zoobank.org:author:90A98A50-327E-4648-9DCE-75709C7A2472 6 urn:lsid:zoobank.org:author:1EB6DE00-9E91-407C-B7C4-34F31F29FD88 7 urn:lsid:zoobank.org:author:6D3AC760-77F2-4CFA-B5C7-665CB07F4CEB 8 urn:lsid:zoobank.org:author:48E53CF3-71C8-403C-BECD-10B20B3C15B4 Abstract. The study of the Portuguese marine ichthyofauna has a long historical tradition, rooted back in the 18th Century. Here we present an annotated checklist of the marine fishes from Portuguese waters, including the area encompassed by the proposed extension of the Portuguese continental shelf and the Economic Exclusive Zone (EEZ). The list is based on historical literature records and taxon occurrence data obtained from natural history collections, together with new revisions and occurrences. -
Highly Diversified Late Cretaceous Fish Assemblage Revealed by Otoliths (Ripley Formation and Owl Creek Formation, Northeast Mississippi, Usa)
Rivista Italiana di Paleontologia e Stratigrafia (Research in Paleontology and Stratigraphy) vol. 126(1): 111-155. March 2020 HIGHLY DIVERSIFIED LATE CRETACEOUS FISH ASSEMBLAGE REVEALED BY OTOLITHS (RIPLEY FORMATION AND OWL CREEK FORMATION, NORTHEAST MISSISSIPPI, USA) GARY L. STRINGER1, WERNER SCHWARZHANS*2 , GEORGE PHILLIPS3 & ROGER LAMBERT4 1Museum of Natural History, University of Louisiana at Monroe, Monroe, Louisiana 71209, USA. E-mail: [email protected] 2Natural History Museum of Denmark, Zoological Museum, Universitetsparken 15, DK-2100, Copenhagen, Denmark. E-mail: [email protected] 3Mississippi Museum of Natural Science, 2148 Riverside Drive, Jackson, Mississippi 39202, USA. E-mail: [email protected] 4North Mississippi Gem and Mineral Society, 1817 CR 700, Corinth, Mississippi, 38834, USA. E-mail: [email protected] *Corresponding author To cite this article: Stringer G.L., Schwarzhans W., Phillips G. & Lambert R. (2020) - Highly diversified Late Cretaceous fish assemblage revealed by otoliths (Ripley Formation and Owl Creek Formation, Northeast Mississippi, USA). Riv. It. Paleontol. Strat., 126(1): 111-155. Keywords: Beryciformes; Holocentriformes; Aulopiformes; otolith; evolutionary implications; paleoecology. Abstract. Bulk sampling and extensive, systematic surface collecting of the Coon Creek Member of the Ripley Formation (early Maastrichtian) at the Blue Springs locality and primarily bulk sampling of the Owl Creek Formation (late Maastrichtian) at the Owl Creek type locality, both in northeast Mississippi, USA, have produced the largest and most highly diversified actinopterygian otolith (ear stone) assemblage described from the Mesozoic of North America. The 3,802 otoliths represent 30 taxa of bony fishes representing at least 22 families. In addition, there were two different morphological types of lapilli, which were not identifiable to species level. -
Appendices Appendices
APPENDICES APPENDICES APPENDIX 1 – PUBLICATIONS SCIENTIFIC PAPERS Aidoo EN, Ute Mueller U, Hyndes GA, and Ryan Braccini M. 2015. Is a global quantitative KL. 2016. The effects of measurement uncertainty assessment of shark populations warranted? on spatial characterisation of recreational fishing Fisheries, 40: 492–501. catch rates. Fisheries Research 181: 1–13. Braccini M. 2016. Experts have different Andrews KR, Williams AJ, Fernandez-Silva I, perceptions of the management and conservation Newman SJ, Copus JM, Wakefield CB, Randall JE, status of sharks. Annals of Marine Biology and and Bowen BW. 2016. Phylogeny of deepwater Research 3: 1012. snappers (Genus Etelis) reveals a cryptic species pair in the Indo-Pacific and Pleistocene invasion of Braccini M, Aires-da-Silva A, and Taylor I. 2016. the Atlantic. Molecular Phylogenetics and Incorporating movement in the modelling of shark Evolution 100: 361-371. and ray population dynamics: approaches and management implications. Reviews in Fish Biology Bellchambers LM, Gaughan D, Wise B, Jackson G, and Fisheries 26: 13–24. and Fletcher WJ. 2016. Adopting Marine Stewardship Council certification of Western Caputi N, de Lestang S, Reid C, Hesp A, and How J. Australian fisheries at a jurisdictional level: the 2015. Maximum economic yield of the western benefits and challenges. Fisheries Research 183: rock lobster fishery of Western Australia after 609-616. moving from effort to quota control. Marine Policy, 51: 452-464. Bellchambers LM, Fisher EA, Harry AV, and Travaille KL. 2016. Identifying potential risks for Charles A, Westlund L, Bartley DM, Fletcher WJ, Marine Stewardship Council assessment and Garcia S, Govan H, and Sanders J.