Atherinomorus [Family-Group Name Used As Valid By: Dyer 1997 [Ref

Total Page:16

File Type:pdf, Size:1020Kb

Atherinomorus [Family-Group Name Used As Valid By: Dyer 1997 [Ref FAMILY Atherinomoridae Dyer & Chernoff, 1996 - silversides, hardyhead silversides [=Atherioninae] Notes: Name in prevailing recent practice Atherioninae Schultz, 1948:3 [ref. 3966] (subfamily) Atherion Atherinomorinae Dyer & Chernoff, 1996:5 [ref. 23238] (subfamily) Atherinomorus [family-group name used as valid by: Dyer 1997 [ref. 23262], Dyer 1998 [ref. 23858], Nelson 2006 [ref. 32486]] GENUS Alepidomus Hubbs, 1944 - silversides [=Alepidomus Hubbs [C. L.] 1944:7] Notes: [ref. 2249]. Masc. Atherina evermanni Eigenmann, 1903. Type by original designation (also monotypic). •Valid as Alepidomus Hubbs 1944 -- (Dyer 2000:101 [ref. 26677], Dyer in Reis et al. 2003:513 [ref. 27061], Campanella et al. 2015:16 [ref. 33711]). Current status: Valid as Alepidomus Hubbs, 1944. Atherinomoridae. Species Alepidomus evermanni (Eigenmann, 1903) – Evermann's alepidomus [=Atherina evermanni Eigenmann [C. H.], 1903:228, Fig. 9] Notes: [Bulletin of the U. S. Fish Commission v. 22 (1902); ref. 1217] San Cristobal, Cuba. Current status: Valid as Alepidomus evermanni (Eigenmann, 1903). Atherinomoridae. Distribution: Western Cuba. Habitat: freshwater. GENUS Atherinomorus Fowler, 1903 - silversides [=Atherinomorus (subgenus of Atherina) Fowler [H. W.], 1903:730, Pranesus Whitley [G. P.], 1930:9, Thoracatherina Fowler [H. W.], 1941:249] Notes: [ref. 1362]. Masc. Atherina laticeps Poey, 1860. Type by original designation (also monotypic). •Valid as Atherinomorus Fowler, 1903 -- (Whitehead & Ivantsoff 1983:361 [ref. 5418], White et al. 1984:360 [ref. 13655], Yoshino in Masuda et al. 1984:119 [ref. 6441], Quignard & Pras in Whitehead et al. 1986:1209 [ref. 13677], Ivantsoff 1986:382 [ref. 6292], Paxton et al. 1989:355 [ref. 12442], Ivantsoff & Crowley 1991:479 [ref. 19162], Castro-Aguirre et al. 1999:199 [ref. 24550], Ivantsoff & Crowley 1999:2114 [ref. 24783], Dyer 2000:101 [ref. 26677], Dyer in Reis et al. 2003:513 [ref. 27061], Paxton et al. 2006:702 [ref. 28995], Kimura et al. 2007:145 [ref. 29157], Kimura 2009:46 [ref. 30426], Kottelat 2013:286 [ref. 33989], Campanella et al. 2015:16 [ref. 33711]). Current status: Valid as Atherinomorus Fowler, 1903. Atherinomoridae. (Pranesus) [ref. 4671]. Masc. Pranesus ogilbyi Whitley, 1930. Type by original designation (also monotypic). •Valid as Pranesus Whitley, 1930 -- (Kiener & Spillmann 1973:578 [ref. 7217]). •Valid but spelled Prasenus -- (Kottelat 1989:16 [ref. 13605]). •Synonym of Atherinomorus Fowler, 1903 -- (Whitehead & Ivantsoff 1983:361 [ref. 5418], Ivantsoff 1986:382 [ref. 6292], Ivantsoff & Crowley 1991:484 [ref. 19162], Dyer in Reis et al. 2003:513 [ref. 27061], Kottelat 2013:286 [ref. 32989]). Current status: Synonym of Atherinomorus Fowler, 1903. Atherinomoridae. (Thoracatherina) [ref. 1438]. Fem. Atherina insularum Jordan & Evermann, 1903. Type by original designation (also monotypic). •Synonym of Atherinomorus Fowler, 1903 -- (Ivantsoff & Crowley 1991:484 [ref. 19162], Dyer in Reis et al. 2003:513 [ref. 27061], Kottelat 2013:286 [ref. 32989]). Current status: Synonym of Atherinomorus Fowler, 1903. Atherinomoridae. Species Atherinomorus aetholepis Kimura et al., 2002 – spatular-scale silverside [=Atherinomorus aetholepis Kimura [S.], Iwatsuki [Y.] & Yoshino [T.], 2002:240, Fig. 1] Notes: [Ichthyological Research v. 49 (no. 3); ref. 26333] Baguala Bay, Ambon Island, Molucca Islands, Indonesia. Current status: Valid as Atherinomorus aetholepis Kimura, Iwatsuki & Yoshino, 2002. Atherinomoridae. Distribution: Eastern Indian Ocean, western Pacific: Indonesia and Philippines. Habitat: marine. Species Atherinomorus crenolepis (Schultz, in Schultz et al., 1953) – crentulated silverside [=Allanetta crenolepis Schultz [L. P.], in Schultz et al., 1953:302, Fig. 46] Notes: [Bulletin of the United States National Museum No. 202, v. 1; ref. 3975] Tara Island, Philippines. Current status: Valid as Atherinomorus crenolepis (Schultz, 1953). Atherinomoridae. Distribution: Western Pacific: Philippines. Habitat: marine. Species Atherinomorus duodecimalis (Valenciennes, in Cuvier & Valenciennes, 1835) – tropical silverside [=Atherina duodecimalis Valenciennes [A.], in Cuvier & Valenciennes, 1835:458, Atherina balabacensis Seale [A.], 1910:498, Pl. 3 (fig. 2)] Notes: [Histoire naturelle des poissons v. 10; ref. 1004] Sri Lanka, Indian Ocean. Current status: Valid as Atherinomorus duodecimalis (Valenciennes, 1835). Atherinomoridae. Distribution: Indo-West Pacific: Sri Lanka to East Indian Region, Vanuatu and New Caledonia. Habitat: brackish, marine. (balabacensis) [The Philippine Journal of Science Section A v. 4 (no. 6) (for 1909); ref. 4000] Balabac Island, Philippines. Current status: Synonym of Atherinomorus duodecimalis (Valenciennes, 1835). Atherinomoridae. Habitat: brackish, marine. Species Atherinomorus endrachtensis (Quoy & Gaimard, 1825) – Eendracht Land silverside [=Atherina endrachtensis Quoy [J. R. C.] & Gaimard [J. P.], 1825:334, Atherina lineata Günther [A.], 1872:398] Notes: [Voyage autour du monde; ref. 3574] Shark Bay, Western Australia [apparently erroneous, probably New Guinea or Waigeo Island]. Current status: Valid as Atherinomorus endrachtensis (Quoy & Gaimard, 1825). Atherinomoridae. Distribution: Western Pacific: Philippines and New Guinea east to Solomon Islands, south to northern Australia and New Caledonia. Habitat: marine. (lineata) [Annals and Magazine of Natural History (Series 4) v. 10 (no. 59) (art. 56); ref. 18194] Cebu, Philippines. Current status: Synonym of Atherinomorus endrachtensis (Quoy & Gaimard, 1825). Atherinomoridae. Distribution: Western Pacific: Indonesia, Philippines and South China Sea (if valid). Habitat: marine. Species Atherinomorus forskalii (Ruppell, 1838) – Red Sea hardyhead silverside [=Atherina forskalii Rüppell [W. P. E. S.], 1838:132, Pl. 33 (fig. 1)] Notes: [Neue Wirbelthiere zu der Fauna von Abyssinien gehörig. Fische des Rothen Meeres; ref. 3844] Jeddah, Saudi Arabia, Red Sea. Current status: Valid as Atherinomorus forskalii (Rüppell, 1838). Atherinomoridae. Distribution: Red Sea endemic; Mediterranean Sea (Red Sea immigrant). Habitat: marine. Species Atherinomorus insularum (Jordan & Evermann, 1903) – Hawaiian Islands silverside [=Atherina insularum Jordan [D. S.] & Evermann [B. W.], 1903:170, Pranesus insularum whitei Schultz [L. P.] in Schultz et al. 1953:307, Fig. 48] Notes: [Bulletin of the U. S. Fish Commission v. 22 (1902); ref. 2450] Honolulu, Oahu Island, Hawaiian Islands. Current status: Valid as Atherinomorus insularum (Jordan & Evermann, 1903). Atherinomoridae. Distribution: Central Pacific: probably Hawaiian Islands. Habitat: marine. (whitei) [Bulletin of the United States National Museum No. 202, v. 1; ref. 3975] Saipan Island, Mariana Islands, western Pacific. Current status: Synonym of Atherinomorus insularum (Jordan & Evermann, 1903). Atherinomoridae. Habitat: marine. Species Atherinomorus lacunosus (Forster, in Bloch & Schneider, 1801) – wide-banded hardyhead silverside [=Atherina lacunosa Forster [J. R.], in Bloch & Schneider, 1801:112, xxxi, Pranesus capricornensis Woodland [D. J.], 1961:540, Fig. 1, Pranesus maculatus Taylor [W. R.], 1964:140, Pl. 26, Hepsetia pinguis mineri Nichols [J. T.] & Roemhild [J.], 1951:57, Fig. 1, Atherina morrisi Jordan [D. S.] & Starks [E. C.], 1906:697, Fig. 3, Pranesus pinguis ruppelli Smith [J. L. B.], 1965:617, Pl. 99 (Fog. b)] Notes: [M. E. Blochii, Systema Ichthyologiae; ref. 471] New Caledonia [Balade, Province Nord, northeastern Grande Terre, southwestern Pacific]. Current status: Valid as Atherinomorus lacunosus (Forster, 1801). Atherinomoridae. Distribution: Red Sea, Indo-West Pacific: East Africa, Seychelles, to Madagascar and Mascarenes east to Hawaiian Islands and Tuamotu Archipelago, north to southern Japan and Ogasawara Islands, south to Western Australia, New South Wales (Australia) and Rapa; Mediterranean Sea (Red Sea immigrant). Habitat: brackish, marine. (capricornensis) [Pacific Science v. 15 (no. 4); ref. 9394] Reef flat on Heron Island, Capricorn Group, Queensland, Australia, Coral Sea, southwestern Pacific. Current status: Synonym of Atherinomorus lacunosus (Forster, 1801). Atherinomoridae. Habitat: brackish, marine. (maculatus) [Fishes of Arnhem Land v. 4; ref. 3498] Coral reef at Yirrkala, station M48-21, Northern Territory, Australia. Current status: Synonym of Atherinomorus lacunosus (Forster, 1801). Atherinomoridae. Habitat: brackish, marine. (mineri) [Marine Life, Occasional Paper 1 (no. 9); ref. 12907] Pago Pago, American Samoa. Current status: Synonym of Atherinomorus lacunosus (Forster, 1801). Atherinomoridae. Habitat: brackish, marine. (morrisi) [Proceedings of the United States National Museum v. 30 (no. 1462); ref. 10666] Miyanoura, Yakushima, Japan. Current status: Synonym of Atherinomorus lacunosus (Forster, 1801). Atherinomoridae. Habitat: brackish, marine. (ruppelli) [Ichthyological Bulletin, Department of Ichthyology, Rhodes University No. 31; ref. 4135] Jeddah, Saudi Arabia, Red Sea. Current status: Synonym of Atherinomorus lacunosus (Forster, 1801). Atherinomoridae. Habitat: brackish, marine. Species Atherinomorus nesogallica (Cuvier, 1829) – Cuvier's silverside [=Atherina nesogallica Cuvier [G.] (ex Commerson), 1829:235, Atherina pectoralis Valenciennes [A.] in Cuvier & Valenciennes 1835:447] Notes: [Le Règne Animal (Edition 2) v. 2; ref. 995] No locality (Reunion). Current status: Valid as Atherinomorus nesogallica (Cuvier, 1829). Atherinomoridae. Distribution: Habitat: brackish, marine. (pectoralis) [Histoire naturelle des poissons v. 10; ref. 1004] Mauritius,
Recommended publications
  • Atheriniformes : Atherinidae
    Atheriniformes: Atherinidae 2111 Atheriniformes: Atherinidae Order ATHERINIFORMES ATHERINIDAE Silversides by L. Tito de Morais, IRD/LEMAR, University of Brest, Plouzané, France; M. Sylla, Centre de Recherches Océanographiques de Dakar-Thiaroye (CRODT), Senegal and W. Ivantsoff (retired), Biology Science, Macquarie University NSW 2109, North Ryde, Australia iagnostic characters: Small, elongate fish, rarely exceeding 15 cm in length. Body elongate and Dsomewhat compressed. Short head, generally flattened dorsally, large eyes, sharp nose, mouth small, oblique and in terminal position, jaws subequal, reaching or slightly exceeding the anterior margin of the eye; premaxilla with ascending process of variable length, with lateral process present or absent; ramus of dentary bone elevated posteriorly or indistinct from anterior part of lower jaw; fine, small and sharp teeth on the jaws, on the roof of mouth (vomer, palatine, pterygoid) or on outside of mouth; 10 to 26 gill rakers long and slender on lower arm of first gill arch. Two well-separated dorsal fins, the first with 6 to 10 thin, flexible spines, located approximately in the middle of the body; the second dorsal and anal fins with a single small weak spine, 1 unbranched soft ray and a variable number of soft rays. Anal fin always originating slightly in advance of second dorsal fin; pectoral fins inserted high on the flanks, directly behind posterior rim of gill cover, with spine greatly reduced and first ray much thicker than those following. Abdomninal pelvic fins with 1 spine and 5 soft rays; forked caudal fin; anus away from the origin of the anal fin. Relatively large scales, cycloid (smooth).
    [Show full text]
  • The Rise and Fall of the Ancient Northern Pike Master Sex Determining Gene
    bioRxiv preprint doi: https://doi.org/10.1101/2020.05.31.125336; this version posted June 1, 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. The rise and fall of the ancient northern pike master sex determining gene Qiaowei Pan1,2, Romain Feron1,2,3, Elodie Jouanno1, Hugo Darras2, Amaury Herpin1, Ben Koop4, Eric Rondeau4, Frederick W. Goetz5, Wesley A. Larson6, Louis Bernatchez7, Mike Tringali8, Stephen S. Curran9, Eric Saillant10, Gael P.J. Denys11,12, Frank A. von Hippel13, Songlin Chen14, J. Andrés López15, Hugo Verreycken16, Konrad Ocalewicz17, Rene Guyomard18, Camille Eche19, Jerome Lluch19, Celine Roques19, Hongxia Hu20, Roger Tabor21, Patrick DeHaan21, Krista M. Nichols22, Laurent Journot23, Hugues Parrinello23, Christophe Klopp24, Elena A. Interesova25, Vladimir Trifonov26, Manfred Schartl27, John Postlethwait28, Yann Guiguen1&. &: Corresponding author. 1. INRAE, LPGP, 35000, Rennes, France. 2. Department of Ecology and Evolution, University of Lausanne,1015, Lausanne, Switzerland. 3. Swiss Institute of Bioinformatics, 1015 Lausanne, Switzerland. 4. Department of Biology, Centre for Biomedical Research, University of Victoria, Victoria, BC, V8W 3N5, Canada. 5. Environmental and Fisheries Sciences Division, Northwest Fisheries Science Center, National Marine Fisheries Service, NOAA, Seattle, WA, United States of America. 6. Fisheries Aquatic Science and Technology Laboratory at Alaska Pacific University. 4101 University Dr, Anchorage, AK 99508. 7. Institut de Biologie Intégrative et des Systèmes (IBIS), Université Laval, Québec, Québec, Canada, G1V 0A6. 8. Fish and Wildlife Conservation Commission, Florida Marine Research Institute, St.
    [Show full text]
  • Age, Growth and Body Condition of Big-Scale Sand Smelt Atherina Boyeri Risso, 1810 Inhabiting a Freshwater Environment: Lake Trasimeno (Italy)
    Knowledge and Management of Aquatic Ecosystems (2015) 416, 09 http://www.kmae-journal.org c ONEMA, 2015 DOI: 10.1051/kmae/2015005 Age, growth and body condition of big-scale sand smelt Atherina boyeri Risso, 1810 inhabiting a freshwater environment: Lake Trasimeno (Italy) M. Lorenzoni(1), D. Giannetto(2),,A.Carosi(1), R. Dolciami(3), L. Ghetti(4), L. Pompei(1) Received September 24, 2014 Revised January 29, 2015 Accepted January 29, 2015 ABSTRACT Key-words: The age, growth and body condition of the big-scale sand smelt (Athe- Population rina boyeri) population of Lake Trasimeno were investigated. In total, dynamics, 3998 specimens were collected during the study and five age classes Lee’s (from 0+ to 4+) were identified. From a subsample of 1017 specimens, phenomenon, there were 583 females, 411 males and 23 juveniles. The equations = − fishery between total length (TL) and weight (W) were: log10 W 2.326 + = − management, 3.139 log10 TL for males and log10 W 2.366 + 3.168 log10 TL for fe- introduced males. There were highly significant differences between the sexes and species, for both sexes the value of b (slope of the log (TL-W regression) was Lake Trasimeno greater than 3 (3.139 for males and 3.168 for females), indicating positive allometric growth. The parameters of the theoretical growth curve were: −1 TLt = 10.03 cm; k = 0.18 yr , t0 = −0.443 yr and Φ = 1.65. Monthly trends of overall condition and the gonadosomatic index (GSI) indicated that the reproductive period occurred from March to September. Analy- sis of back-calculated lengths indicated the occurrence of a reverse Lee’s phenomenon.
    [Show full text]
  • Atherina Presbyter Cuvier of Langstone Harbour, Hampshire
    THE BIOLOGY OF THE BRITISH ATHERINIDAE, WITH PARTICULAR REFERENCE TO ATHERINA PRESBYTER CUVIER OF LANGSTONE HARBOUR, HAMPSHIRE CHRISTOPHER JAMES PALMER, B.Sc. (C.N.A.A.) A thesis presented in candidature for the degree of Doctor of Philosophy of the Council for National Academic Awards DEPARTMENT OF BIOLOGICAL SCIENCES PORTSMOUTH POLYTECHNIC 8004420 SEPTEMBER 1979. CONTENTS Page Abstract ii Acknowledgements J SECTION I GENERAL INTRODUCTION SECTION II STUDY AREAS AND GENERAL METHODS 6 2.1. Study areas and methods of sample capture 6 2.1.1. Langstone Harbour, Hampshire 6 2.1.2. Fawley, Hampshire t1 2.1.3. Medina Estuary, Isle of Wight 11 2.1.4. Oldbury-upon-Severn, Gloucestershire 14 2,1.5. Pembroke Power Station 15 2.1.6. Chapman's Pool, Dorset JS 2.1.7. Lowestoft, Suffolk .15 2.1.8. Jersey, Channel Islands _15 2.2. Preservation of material 15 2.3. Age convention J7 2.4. Body length and weight _17 2.5. Statistical treatments 18 SECTION III TAXONOMY OF THE BRITISH ATHERINIDAE 20 3. 1. Introduction 20 3.2. British literature 21 3.2.1. Comparison with Kiener and Spillmann's 25 key 3.2.2. Other meristics and morphometrics 25 3.3. Methods and materials 25 3.4. Results and discussion 27 3.4.1. Specific identity 27 3.4.2. Geographical variation in A. presbyter 33 around the British Isles 3.4.3. Sexual dimorphism and the effects of age 33 and length on morphometrics 3.4.4. Key modifications 40 Page 3.4.5. Species descriptions 40 3.5.
    [Show full text]
  • Fishes of Terengganu East Coast of Malay Peninsula, Malaysia Ii Iii
    i Fishes of Terengganu East coast of Malay Peninsula, Malaysia ii iii Edited by Mizuki Matsunuma, Hiroyuki Motomura, Keiichi Matsuura, Noor Azhar M. Shazili and Mohd Azmi Ambak Photographed by Masatoshi Meguro and Mizuki Matsunuma iv Copy Right © 2011 by the National Museum of Nature and Science, Universiti Malaysia Terengganu and Kagoshima University Museum All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means without prior written permission from the publisher. Copyrights of the specimen photographs are held by the Kagoshima Uni- versity Museum. For bibliographic purposes this book should be cited as follows: Matsunuma, M., H. Motomura, K. Matsuura, N. A. M. Shazili and M. A. Ambak (eds.). 2011 (Nov.). Fishes of Terengganu – east coast of Malay Peninsula, Malaysia. National Museum of Nature and Science, Universiti Malaysia Terengganu and Kagoshima University Museum, ix + 251 pages. ISBN 978-4-87803-036-9 Corresponding editor: Hiroyuki Motomura (e-mail: [email protected]) v Preface Tropical seas in Southeast Asian countries are well known for their rich fish diversity found in various environments such as beautiful coral reefs, mud flats, sandy beaches, mangroves, and estuaries around river mouths. The South China Sea is a major water body containing a large and diverse fish fauna. However, many areas of the South China Sea, particularly in Malaysia and Vietnam, have been poorly studied in terms of fish taxonomy and diversity. Local fish scientists and students have frequently faced difficulty when try- ing to identify fishes in their home countries. During the International Training Program of the Japan Society for Promotion of Science (ITP of JSPS), two graduate students of Kagoshima University, Mr.
    [Show full text]
  • Ponticola Bathybius (A Goby, No Common Name) Ecological Risk Screening Summary
    Ponticola bathybius (a goby, no common name) Ecological Risk Screening Summary U.S. Fish and Wildlife Service, March 2012 Revised, August 2018 Web Version, 10/28/2019 Photo: K. Abbasi. Licensed under CC BY-SA 3.0. Available: http://eol.org/pages/215017/overview. (August 2018). 1 Native Range and Status in the United States Native Range From Froese and Pauly (2018a): “Former USSR and Asia: Caspian Sea. Restricted to brackish water habitats [Patzner et al. 2011]” According to Naseka and Bogutskaya (2009), P. bathybius is endemic to the whole Caspian Sea. Status in the United States This species has not been reported as introduced or established in the United States. This species was not found in the aquarium trade. Means of Introductions in the United States This species has not been reported as introduced or established in the United States. Remarks According to Eschmeyer et al. (2018), historical synonyms for P. bathybius include Gobius bathybius, Chasar bathybius, and Neogobius bathybius. All synonyms were used to search for information for this report. 1 2 Biology and Ecology Taxonomic Hierarchy and Taxonomic Standing From Froese and Pauly (2018b): “Animalia (Kingdom) > Chordata (Phylum) > Vertebrata (Subphylum) > Gnathostomata (Superclass) > Actinopterygii (Class) > Perciformes (Order) > Gobioidei (Suborder) > Gobiidae (Family) > Gobiinae (Subfamily) > Ponticola (Genus) > Ponticola bathybius (Species)” From Eschmeyer et al. (2018): “bathybius, Gobius […] Current status: Valid as Ponticola bathybius (Kessler 1877).” Size, Weight, and Age Range From Froese and Pauly (2018a): “Max length : 29.3 cm TL male/unsexed; [Abdoli et al. 2009]” Environment From Froese and Pauly (2018a): “Brackish; demersal; depth range ? - 198 m [Eschmeyer 1998].” From Bani et al.
    [Show full text]
  • 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.
    [Show full text]
  • A Dissertation Entitled Evolution, Systematics
    A Dissertation Entitled Evolution, systematics, and phylogeography of Ponto-Caspian gobies (Benthophilinae: Gobiidae: Teleostei) By Matthew E. Neilson Submitted as partial fulfillment of the requirements for The Doctor of Philosophy Degree in Biology (Ecology) ____________________________________ Adviser: Dr. Carol A. Stepien ____________________________________ Committee Member: Dr. Christine M. Mayer ____________________________________ Committee Member: Dr. Elliot J. Tramer ____________________________________ Committee Member: Dr. David J. Jude ____________________________________ Committee Member: Dr. Juan L. Bouzat ____________________________________ College of Graduate Studies The University of Toledo December 2009 Copyright © 2009 This document is copyrighted material. Under copyright law, no parts of this document may be reproduced without the expressed permission of the author. _______________________________________________________________________ An Abstract of Evolution, systematics, and phylogeography of Ponto-Caspian gobies (Benthophilinae: Gobiidae: Teleostei) Matthew E. Neilson Submitted as partial fulfillment of the requirements for The Doctor of Philosophy Degree in Biology (Ecology) The University of Toledo December 2009 The study of biodiversity, at multiple hierarchical levels, provides insight into the evolutionary history of taxa and provides a framework for understanding patterns in ecology. This is especially poignant in invasion biology, where the prevalence of invasiveness in certain taxonomic groups could
    [Show full text]
  • Hotspots, Extinction Risk and Conservation Priorities of Greater Caribbean and Gulf of Mexico Marine Bony Shorefishes
    Old Dominion University ODU Digital Commons Biological Sciences Theses & Dissertations Biological Sciences Summer 2016 Hotspots, Extinction Risk and Conservation Priorities of Greater Caribbean and Gulf of Mexico Marine Bony Shorefishes Christi Linardich Old Dominion University, [email protected] Follow this and additional works at: https://digitalcommons.odu.edu/biology_etds Part of the Biodiversity Commons, Biology Commons, Environmental Health and Protection Commons, and the Marine Biology Commons Recommended Citation Linardich, Christi. "Hotspots, Extinction Risk and Conservation Priorities of Greater Caribbean and Gulf of Mexico Marine Bony Shorefishes" (2016). Master of Science (MS), Thesis, Biological Sciences, Old Dominion University, DOI: 10.25777/hydh-jp82 https://digitalcommons.odu.edu/biology_etds/13 This Thesis is brought to you for free and open access by the Biological Sciences at ODU Digital Commons. It has been accepted for inclusion in Biological Sciences Theses & Dissertations by an authorized administrator of ODU Digital Commons. For more information, please contact [email protected]. HOTSPOTS, EXTINCTION RISK AND CONSERVATION PRIORITIES OF GREATER CARIBBEAN AND GULF OF MEXICO MARINE BONY SHOREFISHES by Christi Linardich B.A. December 2006, Florida Gulf Coast University A Thesis Submitted to the Faculty of Old Dominion University in Partial Fulfillment of the Requirements for the Degree of MASTER OF SCIENCE BIOLOGY OLD DOMINION UNIVERSITY August 2016 Approved by: Kent E. Carpenter (Advisor) Beth Polidoro (Member) Holly Gaff (Member) ABSTRACT HOTSPOTS, EXTINCTION RISK AND CONSERVATION PRIORITIES OF GREATER CARIBBEAN AND GULF OF MEXICO MARINE BONY SHOREFISHES Christi Linardich Old Dominion University, 2016 Advisor: Dr. Kent E. Carpenter Understanding the status of species is important for allocation of resources to redress biodiversity loss.
    [Show full text]
  • Multi-Locus Fossil-Calibrated Phylogeny of Atheriniformes (Teleostei, Ovalentaria)
    Molecular Phylogenetics and Evolution 86 (2015) 8–23 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Multi-locus fossil-calibrated phylogeny of Atheriniformes (Teleostei, Ovalentaria) Daniela Campanella a, Lily C. Hughes a, Peter J. Unmack b, Devin D. Bloom c, Kyle R. Piller d, ⇑ Guillermo Ortí a, a Department of Biological Sciences, The George Washington University, Washington, DC, USA b Institute for Applied Ecology, University of Canberra, Australia c Department of Biology, Willamette University, Salem, OR, USA d Department of Biological Sciences, Southeastern Louisiana University, Hammond, LA, USA article info abstract Article history: Phylogenetic relationships among families within the order Atheriniformes have been difficult to resolve Received 29 December 2014 on the basis of morphological evidence. Molecular studies so far have been fragmentary and based on a Revised 21 February 2015 small number taxa and loci. In this study, we provide a new phylogenetic hypothesis based on sequence Accepted 2 March 2015 data collected for eight molecular markers for a representative sample of 103 atheriniform species, cover- Available online 10 March 2015 ing 2/3 of the genera in this order. The phylogeny is calibrated with six carefully chosen fossil taxa to pro- vide an explicit timeframe for the diversification of this group. Our results support the subdivision of Keywords: Atheriniformes into two suborders (Atherinopsoidei and Atherinoidei), the nesting of Notocheirinae Silverside fishes within Atherinopsidae, and the monophyly of tribe Menidiini, among others. We propose taxonomic Marine to freshwater transitions Marine dispersal changes for Atherinopsoidei, but a few weakly supported nodes in our phylogeny suggests that further Molecular markers study is necessary to support a revised taxonomy of Atherinoidei.
    [Show full text]
  • FAMILY Atherinomoridae Dyer & Chernoff 1996
    FAMILY Atherinomoridae Dyer & Chernoff 1996 - silversides, hardyhead silversides [=Atherioninae] GENUS Alepidomus Hubbs, 1944 - silversides Species Alepidomus evermanni (Eigenmann, 1903) - Evermann's alepidomus GENUS Atherinomorus Fowler, 1903 - silversides [=Pranesus, Thoracatherina] Species Atherinomorus aetholepis Kimura et al., 2002 - spatular-scale silverside Species Atherinomorus crenolepis (Schultz, in Schultz et al., 1953) - crentulated silverside Species Atherinomorus duodecimalis (Valenciennes, in Cuvier & Valenciennes, 1835) – tropical silverside [=balabacensis] Species Atherinomorus endrachtensis (Quoy & Gaimard, 1825) - Eendracht Land silverside [=lineata] Species Atherinomorus forskalii (Ruppell, 1838) - Red Sea hardyhead silverside Species Atherinomorus insularum (Jordan & Evermann, 1903) - Hawaiian Islands silverside [=whitei] Species Atherinomorus lacunosus (Forster, 1801) - Wide-banded hardyhead silverside [=capricornensis, maculatus, mineri, morrisi, ruppelli] Species Atherinomorus nesogallica (Cuvier, 1829) - Cuvier's silverside [=pectoralis] Species Atherinomorus pinguis (Lacepede, 1803) - Narrow-banded hardyhead silverside Species Atherinomorus regina (Seale, 1910) - Culion silverside Species Atherinomorus stipes (Muller & Troschel, in Schomburgk, 1848) - hardyhead silverside [=laticeps, velieana] Species Atherinomorus vaigiensis (Quoy & Gaimard, 1825) - Ogilby's hardyhead silverside [=cylindrica, ogilbyi] GENUS Atherion Jordan & Starks, 1901 - silversides Species Atherion africanum Smith, 1965 - pricklenose silverside
    [Show full text]
  • Training Manual Series No.15/2018
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by CMFRI Digital Repository DBTR-H D Indian Council of Agricultural Research Ministry of Science and Technology Central Marine Fisheries Research Institute Department of Biotechnology CMFRI Training Manual Series No.15/2018 Training Manual In the frame work of the project: DBT sponsored Three Months National Training in Molecular Biology and Biotechnology for Fisheries Professionals 2015-18 Training Manual In the frame work of the project: DBT sponsored Three Months National Training in Molecular Biology and Biotechnology for Fisheries Professionals 2015-18 Training Manual This is a limited edition of the CMFRI Training Manual provided to participants of the “DBT sponsored Three Months National Training in Molecular Biology and Biotechnology for Fisheries Professionals” organized by the Marine Biotechnology Division of Central Marine Fisheries Research Institute (CMFRI), from 2nd February 2015 - 31st March 2018. Principal Investigator Dr. P. Vijayagopal Compiled & Edited by Dr. P. Vijayagopal Dr. Reynold Peter Assisted by Aditya Prabhakar Swetha Dhamodharan P V ISBN 978-93-82263-24-1 CMFRI Training Manual Series No.15/2018 Published by Dr A Gopalakrishnan Director, Central Marine Fisheries Research Institute (ICAR-CMFRI) Central Marine Fisheries Research Institute PB.No:1603, Ernakulam North P.O, Kochi-682018, India. 2 Foreword Central Marine Fisheries Research Institute (CMFRI), Kochi along with CIFE, Mumbai and CIFA, Bhubaneswar within the Indian Council of Agricultural Research (ICAR) and Department of Biotechnology of Government of India organized a series of training programs entitled “DBT sponsored Three Months National Training in Molecular Biology and Biotechnology for Fisheries Professionals”.
    [Show full text]