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Ecography ECOG-01937 Hattab, T., Leprieur, F., Ben Rais Lasram, F., Gravel, D., Le Loc’H, F
Ecography ECOG-01937 Hattab, T., Leprieur, F., Ben Rais Lasram, F., Gravel, D., Le Loc’h, F. and Albouy, C. 2016. Forecasting fine- scale changes in the food-web structure of coastal marine communities under climate change. – Ecography doi: 10.1111/ecog.01937 Supplementary material Forecasting fine-scale changes in the food-web structure of coastal marine communities under climate change by Hattab et al. Appendix 1 List of coastal exploited marine species considered in this study Species Genus Order Family Class Trophic guild Auxis rochei rochei (Risso, 1810) Auxis Perciformes Scombridae Actinopterygii Top predators Balistes capriscus Gmelin, 1789 Balistes Tetraodontiformes Balistidae Actinopterygii Macro-carnivorous Boops boops (Linnaeus, 1758) Boops Perciformes Sparidae Actinopterygii Basal species Carcharhinus plumbeus (Nardo, 1827) Carcharhinus Carcharhiniformes Carcharhinidae Elasmobranchii Top predators Dasyatis pastinaca (Linnaeus, 1758) Dasyatis Rajiformes Dasyatidae Elasmobranchii Top predators Dentex dentex (Linnaeus, 1758) Dentex Perciformes Sparidae Actinopterygii Macro-carnivorous Dentex maroccanus Valenciennes, 1830 Dentex Perciformes Sparidae Actinopterygii Macro-carnivorous Diplodus annularis (Linnaeus, 1758) Diplodus Perciformes Sparidae Actinopterygii Forage species Diplodus sargus sargus (Linnaeus, 1758) Diplodus Perciformes Sparidae Actinopterygii Macro-carnivorous (Geoffroy Saint- Diplodus vulgaris Hilaire, 1817) Diplodus Perciformes Sparidae Actinopterygii Basal species Engraulis encrasicolus (Linnaeus, 1758) Engraulis -
A Practical Handbook for Determining the Ages of Gulf of Mexico And
A Practical Handbook for Determining the Ages of Gulf of Mexico and Atlantic Coast Fishes THIRD EDITION GSMFC No. 300 NOVEMBER 2020 i Gulf States Marine Fisheries Commission Commissioners and Proxies ALABAMA Senator R.L. “Bret” Allain, II Chris Blankenship, Commissioner State Senator District 21 Alabama Department of Conservation Franklin, Louisiana and Natural Resources John Roussel Montgomery, Alabama Zachary, Louisiana Representative Chris Pringle Mobile, Alabama MISSISSIPPI Chris Nelson Joe Spraggins, Executive Director Bon Secour Fisheries, Inc. Mississippi Department of Marine Bon Secour, Alabama Resources Biloxi, Mississippi FLORIDA Read Hendon Eric Sutton, Executive Director USM/Gulf Coast Research Laboratory Florida Fish and Wildlife Ocean Springs, Mississippi Conservation Commission Tallahassee, Florida TEXAS Representative Jay Trumbull Carter Smith, Executive Director Tallahassee, Florida Texas Parks and Wildlife Department Austin, Texas LOUISIANA Doug Boyd Jack Montoucet, Secretary Boerne, Texas Louisiana Department of Wildlife and Fisheries Baton Rouge, Louisiana GSMFC Staff ASMFC Staff Mr. David M. Donaldson Mr. Bob Beal Executive Director Executive Director Mr. Steven J. VanderKooy Mr. Jeffrey Kipp IJF Program Coordinator Stock Assessment Scientist Ms. Debora McIntyre Dr. Kristen Anstead IJF Staff Assistant Fisheries Scientist ii A Practical Handbook for Determining the Ages of Gulf of Mexico and Atlantic Coast Fishes Third Edition Edited by Steve VanderKooy Jessica Carroll Scott Elzey Jessica Gilmore Jeffrey Kipp Gulf States Marine Fisheries Commission 2404 Government St Ocean Springs, MS 39564 and Atlantic States Marine Fisheries Commission 1050 N. Highland Street Suite 200 A-N Arlington, VA 22201 Publication Number 300 November 2020 A publication of the Gulf States Marine Fisheries Commission pursuant to National Oceanic and Atmospheric Administration Award Number NA15NMF4070076 and NA15NMF4720399. -
2017 JMIH Program Book Web Version 6-26-17.Pub
Organizing Societies American Elasmobranch Society 33rd Annual Meeting President: Dean Grubbs Treasurer: Cathy Walsh Secretary: Jennifer Wyffels Editor and Webmaster: David Shiffman Immediate Past President: Chris Lowe American Society of Ichthyologists and Herpetologists 97th Annual Meeting President: Carole Baldwin President Elect: Brian Crother Past President: Maureen A. Donnelly Prior Past President: Larry G. Allen Treasurer: F. Douglas Martin Secretary: Prosanta Chakrabarty Editor: Christopher Beachy Herpetologists’ League 75th Annual Meeting President: David M. Green Immediate Past President: James Spotila Vice-President: David Sever Treasurer: Laurie Mauger Secretary: Renata Platenburg Publications Secretary: Ken Cabarle Communications Secretary: Wendy Palin Herpetologica Editor: Stephen Mullin Herpetological Monographs Editor: Michael Harvey Society for the Study of Amphibians and Reptiles 60th Annual Meeting President: Richard Shine President-Elect: Marty Crump Immediate Past-President: Aaron Bauer Secretary: Marion R. Preest Treasurer: Kim Lovich Publications Secretary: Cari-Ann Hickerson Thank you to our generous sponsor We would like to thank the following: Local Hosts David Hillis, University of Texas at Austin, LHC Chair Dean Hendrickson, University of Texas at Austin Becca Tarvin, University of Texas at Austin Anne Chambers, University of Texas at Austin Christopher Peterson, University of Texas at Austin Volunteers We wish to thank the following volunteers who have helped make the Joint Meeting of Ichthyologists and Herpetologists -
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. -
New Zealand Fishes a Field Guide to Common Species Caught by Bottom, Midwater, and Surface Fishing Cover Photos: Top – Kingfish (Seriola Lalandi), Malcolm Francis
New Zealand fishes A field guide to common species caught by bottom, midwater, and surface fishing Cover photos: Top – Kingfish (Seriola lalandi), Malcolm Francis. Top left – Snapper (Chrysophrys auratus), Malcolm Francis. Centre – Catch of hoki (Macruronus novaezelandiae), Neil Bagley (NIWA). Bottom left – Jack mackerel (Trachurus sp.), Malcolm Francis. Bottom – Orange roughy (Hoplostethus atlanticus), NIWA. New Zealand fishes A field guide to common species caught by bottom, midwater, and surface fishing New Zealand Aquatic Environment and Biodiversity Report No: 208 Prepared for Fisheries New Zealand by P. J. McMillan M. P. Francis G. D. James L. J. Paul P. Marriott E. J. Mackay B. A. Wood D. W. Stevens L. H. Griggs S. J. Baird C. D. Roberts‡ A. L. Stewart‡ C. D. Struthers‡ J. E. Robbins NIWA, Private Bag 14901, Wellington 6241 ‡ Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington, 6011Wellington ISSN 1176-9440 (print) ISSN 1179-6480 (online) ISBN 978-1-98-859425-5 (print) ISBN 978-1-98-859426-2 (online) 2019 Disclaimer While every effort was made to ensure the information in this publication is accurate, Fisheries New Zealand does not accept any responsibility or liability for error of fact, omission, interpretation or opinion that may be present, nor for the consequences of any decisions based on this information. 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 website at http://www.mpi.govt.nz/news-and-resources/publications/ A higher resolution (larger) PDF of this guide is also available by application to: [email protected] Citation: McMillan, P.J.; Francis, M.P.; James, G.D.; Paul, L.J.; Marriott, P.; Mackay, E.; Wood, B.A.; Stevens, D.W.; Griggs, L.H.; Baird, S.J.; Roberts, C.D.; Stewart, A.L.; Struthers, C.D.; Robbins, J.E. -
Order ZEIFORMES PARAZENIDAE Parazens P.C
click for previous page Zeiformes: Parazenidae 1203 Order ZEIFORMES PARAZENIDAE Parazens P.C. Heemstra, South African Institute for Aquatic Biodiversity, South Africa iagnostic characters: Small to moderate-sized (to 30 cm) oblong fishes, the head and body com- Dpressed; body depth slightly less than head length, contained 2.6 to 2.9 times in standard length; head naked, the bones thin and soft; opercular bones weakly serrate; mouth large, terminal, the upper jaw extremely protrusile; maxilla widely expanded posteriorly, and mostly exposed when mouth is closed; no supramaxilla; jaws with 1 or 2 rows of small, slender, conical teeth; vomer with a few short stout teeth;gill rakers (including rudiments) 2 on upper limb, 8 on lower limb.Eye diameter about 1/3 head length and slightly less than snout length.Branchiostegal rays 7.Dorsal fin divided, with 8 slender spines and 26 to 30 soft rays; anal fin with 1 minute spine and 30 to 32 soft rays; dorsal-, anal-, and pectoral-fin rays un- branched; caudal fin forked, with 11 principal rays and 9 branched rays; pectoral fin with 15 or 16 rays, shorter than eye diameter; pelvic fins with 1 unbranched and 5 or 6 branched soft rays, but no spine, fin origin posterior to a vertical at pectoral-fin base. Scales moderate in size, weakly ctenoid, and deciduous; 2 lateral lines originating on body at upper end of operculum and running posteriorly about 4 scale rows apart, gradually converging to form a single line on caudal peduncle. Caudal peduncle stout, the least depth about equal to its length and slightly less than eye diameter.Vertebrae 34.Colour: body reddish or silvery; large black blotch on anterior margin of dorsal fin. -
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 -
Fish Bulletin 161. California Marine Fish Landings for 1972 and Designated Common Names of Certain Marine Organisms of California
UC San Diego Fish Bulletin Title Fish Bulletin 161. California Marine Fish Landings For 1972 and Designated Common Names of Certain Marine Organisms of California Permalink https://escholarship.org/uc/item/93g734v0 Authors Pinkas, Leo Gates, Doyle E Frey, Herbert W Publication Date 1974 eScholarship.org Powered by the California Digital Library University of California STATE OF CALIFORNIA THE RESOURCES AGENCY OF CALIFORNIA DEPARTMENT OF FISH AND GAME FISH BULLETIN 161 California Marine Fish Landings For 1972 and Designated Common Names of Certain Marine Organisms of California By Leo Pinkas Marine Resources Region and By Doyle E. Gates and Herbert W. Frey > Marine Resources Region 1974 1 Figure 1. Geographical areas used to summarize California Fisheries statistics. 2 3 1. CALIFORNIA MARINE FISH LANDINGS FOR 1972 LEO PINKAS Marine Resources Region 1.1. INTRODUCTION The protection, propagation, and wise utilization of California's living marine resources (established as common property by statute, Section 1600, Fish and Game Code) is dependent upon the welding of biological, environment- al, economic, and sociological factors. Fundamental to each of these factors, as well as the entire management pro- cess, are harvest records. The California Department of Fish and Game began gathering commercial fisheries land- ing data in 1916. Commercial fish catches were first published in 1929 for the years 1926 and 1927. This report, the 32nd in the landing series, is for the calendar year 1972. It summarizes commercial fishing activities in marine as well as fresh waters and includes the catches of the sportfishing partyboat fleet. Preliminary landing data are published annually in the circular series which also enumerates certain fishery products produced from the catch. -
Zeidae Rafinesque, 1815 - True Dories [=Zeusidi Rafinesque, 1810, Zedia Rafinesque, 1815, ?Aplodia Rafinesque, 1815] Notes: Zeusidi Rafinesque, 1810B:15 [Ref
FAMILY Zeidae Rafinesque, 1815 - true dories [=Zeusidi Rafinesque, 1810, Zedia Rafinesque, 1815, ?Aplodia Rafinesque, 1815] Notes: Zeusidi Rafinesque, 1810b:15 [ref. 3595] (ordine) Zeus [published not in latinized form before 1900; not available, Article 11.7.2] Zedia Rafinesque, 1815:83 [ref. 3584] (family) Zeus [stem corrected to Ze- by Latreille 1825:131 [ref. 31889], confirmed by Bonaparte 1831:158, 174 [ref. 4978]; stem changed to Zen- by Lowe 1839:82 [ref. 2829], confirmed by Gill 1873:787 [ref. 17631]; stem Ze- confirmed by Nelson 1976:192 [ref. 32838] and by Nelson 2006:307 [ref. 32486]] ?Aplodia Rafinesque, 1815:84 [ref. 3584] (subfamily) ? Zeus [no stem of the type genus, not available, Article 11.7.1.1] GENUS Zenopsis Gill, 1862 - John dories [=Zenopsis Gill [T. N.], 1862:126, Parazenopsis Cligny [A.], 1909:874 [1]] Notes: [ref. 1659]. Fem. Zeus nebulosus Temminck & Schlegel, 1845. Type by original designation (also monotypic). •Valid as Zenopsis Gill, 1862 -- (Wheeler 1973:349 [ref. 7190], Heemstra 1980:11 [ref. 14195], Machida in Masuda et al. 1984:118 [ref. 6441], Quéro in Whitehead et al. 1986:770 [ref. 13676], Heemstra 1986:437 [ref. 5660], Paxton et al. 1989:389 [ref. 12442], Parin 1989 [ref. 14116], Gomon et al. 1994:420 [ref. 22532], Heemstra 1999:2259 [ref. 24791], Tyler et al. 2003:36 [ref. 26742], Heemstra 2003:1209 [ref. 27043], Nakabo et al.2006:91 [ref. 28907], Paxton et al. 2006:800 [ref. 29077], Bray 2008:439 [ref. 30620], Shinohara et al. 2011:41 [ref. 31715]). Current status: Valid as Zenopsis Gill, 1862. Zeidae. (Parazenopsis) [ref. 850]. -
Orange Roughy New Zealand
Orange Roughy Hoplostethus atlanticus Image ©Monterey Bay Aquarium New Zealand Bottom Trawl July 21, 2014 Andy Woolmer and Jess Woo, Consulting Researcher 2 About Seafood Watch® The Monterey Bay Aquarium Seafood Watch® program evaluates the ecological sustainability of wild- caught and farmed seafood commonly found in the North American marketplace. Seafood Watch defines sustainable seafood as originating from sources, whether wild-caught or farmed, which can maintain or increase production in the long-term without jeopardizing the structure or function of affected ecosystems. The program’s mission is to engage and empower consumers and businesses to purchase environmentally responsible seafood fished or farmed in ways that minimize their impact on the environment or are in a credible improvement project with the same goal. Each sustainability recommendation is supported by a seafood report. Each report synthesizes and analyzes the most current ecological, fisheries and ecosystem science on a species, then evaluates this information against the program’s Sustainability Criteria to arrive at a recommendation of “Best Choice,” “Good Alternative,” or “Avoid.” In producing the seafood reports, Seafood Watch utilizes research published in academic, peer-reviewed journals whenever possible. Other sources of information include government technical publications, fishery management plans and supporting documents, and other scientific reviews of ecological sustainability. Seafood Watch research analysts also communicate with ecologists, fisheries and aquaculture scientists, and members of industry and conservation organizations when evaluating fisheries and aquaculture practices. Capture fisheries and aquaculture practices are highly dynamic; as the scientific information on each species changes, Seafood Watch’s sustainability recommendations and the underlying seafood reports will be updated to reflect these changes. -
Randal Singer, Ph.D
CURRICULUM VITAE Randal Singer, Ph.D. The University of Michigan Email: [email protected]; Tel: (352) 209-1024 Office: 1421 Research Museums Center, 3600 Varsity Drive, Ann Arbor, MI 48108-2228 Website: https://randchovy.wixsite.com/randalsinger EDUCATION 2019 PhD, Interdisciplinary Ecology The University of Florida/iDigBio, Gainesville, FL Thesis advisor: Lawrence M. Page Dissertation: An Interdisciplinary Approach to Increasing the Sustainability of Biodiversity Collections 2013 M.S., Zoology The University of Florida, Gainesville, FL Advisor: Lawrence M. Page Thesis: A Revision of the genus Acanthocobitis (Peters 1861) with description of a new genus: Paracanthocobitis (Teleostei: Nemacheilidae) 2008 B.S., Ecology The University of Georgia, Athens, GA Senior thesis: Tracing carbon flow in deep-sea whale-fall communities using STELLA. PROFESSIONAL APPOINTMENTS/EMPLOYMENT 2019-Present The University of Michigan– Asst. Research Scientist/Collection Manager, Fishes Management, curation, and coordination of collection resources and activities Facilitation of collections based research, education and outreach Aiding research uses of collection through visits and external loans Personal scientific research on fishes (734) 936-3754 2015-2019 The University of Florida/iDigBio – PhD Candidate Conducting informatics research using specimen data Advocating for collections care and use Organizing workshops and webinars for iDigBio Representing iDigBio at conferences and events (352) 273-1374 2013-2015 University of Alabama – Collections Manager, Ichthyology Responsible for specimen cataloguing and curation Oversee all activities of the fish and herpetology collections Conduct and aid in research both in and outside of the collection Aiding in public outreach and specimen loans for research (205) 348-1822 2010-2013 Florida Museum of Natural History – Asst. -
Diet of the Australian Sea Lion (Neophoca Cinerea): an Assessment of Novel DNA-Based and Contemporary Methods to Determine Prey Consumption
Diet of the Australian sea lion (Neophoca cinerea): an assessment of novel DNA-based and contemporary methods to determine prey consumption Kristian John Peters BSc (hons), LaTrobe University, Victoria Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy University of Adelaide (October, 2016) 2 DECLARATION OF ORIGINALITY I certify that this work contains no material which has been accepted for the award of any other degree or diploma in my name, in any university or other tertiary institution and, to the best of my knowledge and belief, contains no material previously published or written by another person, except where due reference has been made in the text. In addition, I certify that no part of this work will, in the future, be used in a submission in my name, for any other degree or diploma in any university or other tertiary institution without the prior approval of the University of Adelaide and where applicable, any partner institution responsible for the joint-award of this degree. I give consent to this copy of my thesis when deposited in the University Library, being made available for loan and photocopying, subject to the provisions of the Copyright Act 1968. I acknowledge that copyright of published works contained within this thesis resides with the copyright holder(s) of those works. I also give permission for the digital version of my thesis to be made available on the web, via the University’s digital research repository, the Library Search and also through web search engines, unless permission has been granted by the University to restrict access for a period of time.