New Records of Deep-Water Cnidaria (Scleractinia & Antipatharia) from the Gulf of Mexico Stephen D

Total Page:16

File Type:pdf, Size:1020Kb

New Records of Deep-Water Cnidaria (Scleractinia & Antipatharia) from the Gulf of Mexico Stephen D Northeast Gulf Science Volume 13 Article 1 Number 1 Number 1 12-1993 New Records of Deep-Water Cnidaria (Scleractinia & Antipatharia) from the Gulf of Mexico Stephen D. Cairns Smithsonian Institution Dennis M. Opresko Oak Ridge National Laboratory Thomas S. Hopkins University of Alabama William W. Schroeder University of Alabama DOI: 10.18785/negs.1301.01 Follow this and additional works at: https://aquila.usm.edu/goms Recommended Citation Cairns, S. D., D. M. Opresko, T. S. Hopkins and W. W. Schroeder. 1993. New Records of Deep-Water Cnidaria (Scleractinia & Antipatharia) from the Gulf of Mexico. Northeast Gulf Science 13 (1). Retrieved from https://aquila.usm.edu/goms/vol13/iss1/1 This Article is brought to you for free and open access by The Aquila Digital Community. It has been accepted for inclusion in Gulf of Mexico Science by an authorized editor of The Aquila Digital Community. For more information, please contact [email protected]. Cairns et al.: New Records of Deep-Water Cnidaria (Scleractinia & Antipatharia) Northeast Gulf Science Vol. 13, No.1 December 1993 p. 1·11 NEW RECORDS OF DEEP·WATER CNIDARIA (SCLERACTINIA & ANTIPATHARIA) FROM THE GULF OF MEXICO Stephen D. Cairns Department of Invertebrate Zoology, Smithsonian Institution Washington, D.C. 20556 and Dennis M. Opresko Health Sciences Research Division, Oak Ridge National Laboratory Oak Ridge, Tennessee 37930 and Thomas S. Hopkins* Department of Biological Sciences and Marine Science Program, The University of Alabama Tuscaloosa, AL 35487 and William W. Schroeder Marine Science Program, The University of Alabama Marine Environmental Sciences Consortium Box 369, Dauphin Island, AL 36528 ABSTRACT: Slxty·three species of azooxanthellate acleractlnlana and 26 species of antlpatharlana are recorded from the Gulf of Mexico. This report constitutes the first Inventory of Antlpatharla within the geographic boundaries of the Gulf of Mexico whose southern limits are the Yucatan Straits to the south and the Florida Straits to the east. Thirteen range ex· tensions of azooxanthellate species of the Order Scleractinia, and 28 species of the Order Antlpatharla are reported. With respect to new recorda, we report four new records of azoox· anthelate acleractlnlana and six new recorda of antlpatharlana from the outer continentia! shelf. One of the species, Slbopathes macrosplna Opreako, 1993, represents a new species In the western Atlantic region and appears related to Slbopathes gephura Van Pesch, 1914. The Gulf acleractlnlan fauna constitutes 54% of those known from the western Atlantic; the antlpatharlan fauna constitutes 93% of the western Atlantic fauna. These two groups are moat diverse (55·56 species) In the regions of the Gulf adjacent to the Caribbean Sea and Atlantic Ocean (subdivisions I and VI). Diversity gradually decreases towards the western Gulf. Only six species are known from subdivision IV (east Mexico shelf and slope) and 23 species are recorded from subdivision V (Campeche Bank, Mexico). As the deep water regions of the and Soto, 1982; Rezak, et al., 1985; Tun· Gulf of Mexico have become better nell, 1989), a total of 105 scleractinian known through dredging and submersi· species is now recorded from the Gulf ble collections, there has been a steady of Mexico. This figure accounts for 54% increase in the number of benthic of the approximately 195 species of cnidarians recorded from this region. The Scleractinia known from the western number of azooxanthellate Scleractinia Atlantic (Cairns, 1979). Thirteen range ex­ (ahermatypes) known from the Gulf has tensions of azooxanthellate Scleractinia risen from 36 (Cairns, 1977), to 58 (Viada within the Gulf are reported herein (Table and Cairns, 1987), to 63 (this paper). By 1). They include four new records for the including the 42 species of zooxan· Gulf: Madracis pharensis pharensis, thellate (hermatypic) Scleractinia known Caryophyllia barbadenis, Polycyathus from the Gulf (Grimm and Hopkins, 1977; senegalensis, and Asterosmi/ia Zlatarski and Estalella, 1982; Castaiiares marchadi. 1 Published by The Aquila Digital Community, 1993 1 Gulf of Mexico Science, Vol. 13 [1993], No. 1, Art. 1 2 Cairns, S. D., et al Twenty-six species of Antipatharia connecting Key West, Florida to the are recorded from the Gulf of Mexico, closest point on the Cuban coast (ap· and they const,itute about 93% of the proximately 81 °48'W) and the shortest western Atlantic fauna. The following six line between western Cuba and nor­ species are new records for the Gulf: An· theastern Yucatan, Mexico (See Cairns, tlpathes columnaris, Antlpathes desbon­ 1978a). The Gulf is further subdivided ni, Antipathes gracilis, Antipathes hirta, into six areas (Figure 1) to facilitate Bathypathes patula, and Sibopathes geographic categorization: I) from the macrosplna. Twenty-eight subdivisional Florida Keys to Apalachee Bay, Florida, range extensions are also reported II) from Apalachee Bay to the Mississippi (Table 1). River Delta, Ill) from the Delta to the Texas-Mexico border, IV) from that MATERIALS AND METHODS border to the Tabasco-Campeche, Mexico border, V) the Campeche Bank, Abbreviations used in the text in· and VI) the Yucatan Channel and off elude: ACSESS, Alabama Coastal Shelf northwest Cuba to 81 °48'W. Environmental Science Study, Dauphin Regarding azooxanthellate Scler­ Island, AL; CSA, Continentia! Shelf actinia, the following check list (Table 1) Associates, Jupiter, Florida; JSL, is an update of Cairns (1978a). In many Johnson-Sea-Link I research submersi­ cases, revised nomenclature has been ble, Harbor Branch Oceanographic In· provided. Records previously docu­ sitution, Ft. Pierce, Florida; SIO, Scripps mented in Cairns (1978a) are designated Institution of Oceangraphy; SOFLA, with an X in Table 1. All additions to Southwest Florida Shelf Ecosystem Table 1 are indicated by a number keyed Study, Mineral Management Services; to the following sources: 1) Ludwick and UA-DISL, University of Alabama, Dauphin Walton (1957), a previously overlooked Island Sea Lab, Alabama; and USNM, paper having several early records for United States National Museum (now area I. These are: a) Madracis mirabilis NMNH, National Museum of Natural ( = M. asperu/a); b) Bathycyathus sp. ( = History). Pourta/osmilia conferta); and c) Ocul/na The specimens that form the basis disticha ( =Madrepora carolina); 2) of the range extensions originate Moore (1958), in a previously overlooked primarily from three sources: 1) a paper reported Astrangia brasiliensis ( = Johnson-Sea-Link submersible cruise A. solltaria) from Blanquilla Reef, south· south of Louisiana in September 1989, western Gulf, area IV; 3) Weisbord (1974}, the specimens of which are deposited at in a previously overlooked paper pro­ the USNM, 2) UA-DISL specimens col· vided a range extension of Phyllangia lected south of Alabama and northwest americana in area IV; 4) Cairns (1978b); Florida, from the ACSESS program and 5) Cairns (1979); 6) Zlatarski and Estalella two JSL cruises (1987, 1991), and 3) R/V (1982}, area VI; 7) Rezak, et al. (1985}, area Oregon, R/V Pelican, R/V Silver Bay, R/V Ill; 8) Viada and Cairns (i987), area Ill; 9) Verrill, and other miscellaneous collec­ Tunnell (1989); and 10) this paper: 10a· tions such as Continental Shelf Johnson-Sea-Link I 1989 cruise off Associates (CSA), Minerals Management Louisiana; 10b-UA·DISL specimens; 10c­ Service (SOFLA}, Texas A&M (TAMU}, S//ver Bay station 1125; and 10d-USNM and materials deposited at the USNM. general collections. Annotated records The southeastern limits of the Gulf are given below for category 10, which of Mexico are defined as a line constitute the subdivisional range exten- https://aquila.usm.edu/goms/vol13/iss1/1 2 DOI: 10.18785/negs.1301.01 Cairns et al.: New Records of Deep-Water Cnidaria (Scleractinia & Antipatharia) Deep Water Cnideria 3 Figure 1. Map of the Gulf of Mexico showing the six geographic subdivisions (Roman numerals) used in this paper and most of the stations (Cardinal numerals) from which specimens were collected. The 100 fathom (183m) isobath is indicated. Abbreviations: ACSESS (see text); Alb, U.S.F.C.S. Albatross; JSL (see text); 0, RIV Oregon; Pel, RIV Pelican; SB, R/V Silver Bay; SOFLA (see text). sions with the Gulf. Subdivision 1: Florida Keys to Apalachee Sources of all antipatharian records Bay, Florida are indicated in Table 1 in the following Antipatharia manner: A, Opr~sko (1971); B, Opresko (1974); C, Rezak et al. (1985); D, Johnson­ Antipathes atlantica Gray, 1857: Sea-Link 1989 cruise off Louisiana; E, Previously known from the West Indies USNM collections; F, CSA, (unpublished and the northwestern Gulf of Mexico, data); G, UA-DISL; and H, Opresko and 30-115 m (Brook, 1889; Warner, 1981; Cairns (1992). Annotated records are Rezak, et al., 1985). Unpublished records given below only for sources 0-G, which at the University of Miami indicate a constitute the subdivisional range exten­ broad distribution throughout the Carib· sions within the Gulf. bean, 10-30 m. This species is difficult to distinguish from Antipathes gracilis (see Warner, 1981). - New Record: CSA, Range Extensions 25°15'N, 83°40'W (Pulley Ridge, Published by The Aquila Digital Community, 1993 3 Gulf of Mexico Science, Vol. 13 [1993], No. 1, Art. 1 4 Cairns, S. D., et al Table 1. Checklist and distribution of azooxanthellate Scleractinia and Antlpatharla known from the Gulf of Mexico. An asterisk denotes a new record for the Gulf. See preceding text for meaning of letters and numbers. Geographic Subdlvlson II Ill IV
Recommended publications
  • MARINE FAUNA and FLORA of BERMUDA a Systematic Guide to the Identification of Marine Organisms
    MARINE FAUNA AND FLORA OF BERMUDA A Systematic Guide to the Identification of Marine Organisms Edited by WOLFGANG STERRER Bermuda Biological Station St. George's, Bermuda in cooperation with Christiane Schoepfer-Sterrer and 63 text contributors A Wiley-Interscience Publication JOHN WILEY & SONS New York Chichester Brisbane Toronto Singapore ANTHOZOA 159 sucker) on the exumbrella. Color vari­ many Actiniaria and Ceriantharia can able, mostly greenish gray-blue, the move if exposed to unfavorable condi­ greenish color due to zooxanthellae tions. Actiniaria can creep along on their embedded in the mesoglea. Polyp pedal discs at 8-10 cm/hr, pull themselves slender; strobilation of the monodisc by their tentacles, move by peristalsis type. Medusae are found, upside­ through loose sediment, float in currents, down and usually in large congrega­ and even swim by coordinated tentacular tions, on the muddy bottoms of in­ motion. shore bays and ponds. Both subclasses are represented in Ber­ W. STERRER muda. Because the orders are so diverse morphologically, they are often discussed separately. In some classifications the an­ Class Anthozoa (Corals, anemones) thozoan orders are grouped into 3 (not the 2 considered here) subclasses, splitting off CHARACTERISTICS: Exclusively polypoid, sol­ the Ceriantharia and Antipatharia into a itary or colonial eNIDARIA. Oral end ex­ separate subclass, the Ceriantipatharia. panded into oral disc which bears the mouth and Corallimorpharia are sometimes consid­ one or more rings of hollow tentacles. ered a suborder of Scleractinia. Approxi­ Stomodeum well developed, often with 1 or 2 mately 6,500 species of Anthozoa are siphonoglyphs. Gastrovascular cavity compart­ known. Of 93 species reported from Ber­ mentalized by radially arranged mesenteries.
    [Show full text]
  • Checklist of Fish and Invertebrates Listed in the CITES Appendices
    JOINTS NATURE \=^ CONSERVATION COMMITTEE Checklist of fish and mvertebrates Usted in the CITES appendices JNCC REPORT (SSN0963-«OStl JOINT NATURE CONSERVATION COMMITTEE Report distribution Report Number: No. 238 Contract Number/JNCC project number: F7 1-12-332 Date received: 9 June 1995 Report tide: Checklist of fish and invertebrates listed in the CITES appendices Contract tide: Revised Checklists of CITES species database Contractor: World Conservation Monitoring Centre 219 Huntingdon Road, Cambridge, CB3 ODL Comments: A further fish and invertebrate edition in the Checklist series begun by NCC in 1979, revised and brought up to date with current CITES listings Restrictions: Distribution: JNCC report collection 2 copies Nature Conservancy Council for England, HQ, Library 1 copy Scottish Natural Heritage, HQ, Library 1 copy Countryside Council for Wales, HQ, Library 1 copy A T Smail, Copyright Libraries Agent, 100 Euston Road, London, NWl 2HQ 5 copies British Library, Legal Deposit Office, Boston Spa, Wetherby, West Yorkshire, LS23 7BQ 1 copy Chadwick-Healey Ltd, Cambridge Place, Cambridge, CB2 INR 1 copy BIOSIS UK, Garforth House, 54 Michlegate, York, YOl ILF 1 copy CITES Management and Scientific Authorities of EC Member States total 30 copies CITES Authorities, UK Dependencies total 13 copies CITES Secretariat 5 copies CITES Animals Committee chairman 1 copy European Commission DG Xl/D/2 1 copy World Conservation Monitoring Centre 20 copies TRAFFIC International 5 copies Animal Quarantine Station, Heathrow 1 copy Department of the Environment (GWD) 5 copies Foreign & Commonwealth Office (ESED) 1 copy HM Customs & Excise 3 copies M Bradley Taylor (ACPO) 1 copy ^\(\\ Joint Nature Conservation Committee Report No.
    [Show full text]
  • Spatial and Temporal Variations in Community Structure of the Demersal Macrofauna of a Subtropical Estuary (Louisiana)
    Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1982 Spatial and Temporal Variations in Community Structure of the Demersal Macrofauna of a Subtropical Estuary (Louisiana). Thomas C. Shirley Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Shirley, Thomas C., "Spatial and Temporal Variations in Community Structure of the Demersal Macrofauna of a Subtropical Estuary (Louisiana)." (1982). LSU Historical Dissertations and Theses. 3821. https://digitalcommons.lsu.edu/gradschool_disstheses/3821 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. INFORMATION TO USERS This reproduction was made from a copy of a document sent to us for microfilming. While the most advanced technology has been used to photograph and reproduce this document, the quality of the reproduction is heavily dependent upon the quality of the material submitted. The following explanation of techniques is provided to help clarify markings or notations which may appear on this reproduction. 1.The sign or “target” for pages apparently lacking from the document photographed is “Missing Page(s)”. If it was possible to obtain the missing page(s) or section, they are spliced into the film along with adjacent pages. This may have necessitated cutting through an image and duplicating adjacent pages to assure complete continuity. 2. When an image on the film is obliterated with a round black mark, it is an indication of either blurred copy because of movement during exposure, duplicate copy, or copyrighted materials that should not have been filmed.
    [Show full text]
  • OCS Study BOEM 2017-024
    OCS Study BOEM 2017-024 Deepwater Reconnaissance of Potentially Sensitive Biological Features Surrounding Shelf-Edge Topographical Banks in the Northern Gulf of Mexico U.S. Department of the Interior Bureau of Ocean Energy Management Gulf of Mexico OCS Region OCS Study BOEM 2017-024 Deepwater Reconnaissance of Potentially Sensitive Biological Features Surrounding Shelf-Edge Topographical Banks in the Northern Gulf of Mexico Author Paul Sammarco Prepared under BOEM Contract M11AC00005 by Louisiana Universities Marine Consortium 8124 Highway 56 Baton Rouge, LA 70344-2110 Published by U.S. Department of the Interior New Orleans, LA Bureau of Ocean Energy Management February 2017 Gulf of Mexico OCS Region DISCLAIMER This report was prepared under contract between the Bureau of Ocean Energy Management (BOEM) and Louisiana Universities Marine Consortium (LUMCON). This report has been technically reviewed by BOEM, and it has been approved for publication. Approval does not necessarily signify that the contents reflect the views and policies of BOEM, nor does mention of trade names or commercial products constitute endorsement or recommendation for use. REPORT AVAILABILITY To download a PDF file of this Gulf of Mexico OCS Region report, go to the U.S. Department of the Interior, Bureau of Ocean Energy Management, Environmental Studies Program Information System website and search on OCS Study BOEM 2017-024. This report can be viewed at select Federal Depository Libraries. It can also be obtained from the National Technical Information Service; the contact information is below. U.S. Department of Commerce National Technical Information Service 5301 Shawnee Rd. Springfield, Virginia 22312 Phone: (703) 605-6000, 1(800)553-6847 Fax: (703) 605-6900 Website: http://www.ntis.gov/ CITATION Sammarco, Paul W.
    [Show full text]
  • +Tuhinga 27-2016 Vi:Layout 1
    27 2016 2016 TUHINGA Records of the Museum of New Zealand Te Papa Tongarewa Tuhinga: Records of the Museum of New Zealand Te Papa Tongarewa The journal of scholarship and mätauranga Number 27, 2016 Tuhinga: Records of the Museum of New Zealand Te Papa Tongarewa is a peer-reviewed publication, published annually by Te Papa Press PO Box 467, Wellington, New Zealand TE PAPA ® is the trademark of the Museum of New Zealand Te Papa Tongarewa Te Papa Press is an imprint of the Museum of New Zealand Te Papa Tongarewa Tuhinga is available online at www.tepapa.govt.nz/tuhinga It supersedes the following publications: Museum of New Zealand Records (1171-6908); National Museum of New Zealand Records (0110-943X); Dominion Museum Records; Dominion Museum Records in Ethnology. Editorial board: Catherine Cradwick (editorial co-ordinator), Claudia Orange, Stephanie Gibson, Patrick Brownsey, Athol McCredie, Sean Mallon, Amber Aranui, Martin Lewis, Hannah Newport-Watson (Acting Manager, Te Papa Press) ISSN 1173-4337 All papers © Museum of New Zealand Te Papa Tongarewa 2016 Published June 2016 For permission to reproduce any part of this issue, please contact the editorial co-ordinator,Tuhinga, PO Box 467, Wellington. Cover design by Tim Hansen Typesetting by Afineline Digital imaging by Jeremy Glyde Tuhinga: Records of the Museum of New Zealand Te Papa Tongarewa Number 27, 2016 Contents A partnership approach to repatriation: building the bridge from both sides 1 Te Herekiekie Herewini and June Jones Mäori fishhooks at the Pitt Rivers Museum: comments and corrections 10 Jeremy Coote Response to ‘Mäori fishhooks at the Pitt Rivers Museum: comments 20 and corrections’ Chris D.
    [Show full text]
  • Deep‐Sea Coral Taxa in the U.S. Gulf of Mexico: Depth and Geographical Distribution
    Deep‐Sea Coral Taxa in the U.S. Gulf of Mexico: Depth and Geographical Distribution by Peter J. Etnoyer1 and Stephen D. Cairns2 1. NOAA Center for Coastal Monitoring and Assessment, National Centers for Coastal Ocean Science, Charleston, SC 2. National Museum of Natural History, Smithsonian Institution, Washington, DC This annex to the U.S. Gulf of Mexico chapter in “The State of Deep‐Sea Coral Ecosystems of the United States” provides a list of deep‐sea coral taxa in the Phylum Cnidaria, Classes Anthozoa and Hydrozoa, known to occur in the waters of the Gulf of Mexico (Figure 1). Deep‐sea corals are defined as azooxanthellate, heterotrophic coral species occurring in waters 50 m deep or more. Details are provided on the vertical and geographic extent of each species (Table 1). This list is adapted from species lists presented in ʺBiodiversity of the Gulf of Mexicoʺ (Felder & Camp 2009), which inventoried species found throughout the entire Gulf of Mexico including areas outside U.S. waters. Taxonomic names are generally those currently accepted in the World Register of Marine Species (WoRMS), and are arranged by order, and alphabetically within order by suborder (if applicable), family, genus, and species. Data sources (references) listed are those principally used to establish geographic and depth distribution. Only those species found within the U.S. Gulf of Mexico Exclusive Economic Zone are presented here. Information from recent studies that have expanded the known range of species into the U.S. Gulf of Mexico have been included. The total number of species of deep‐sea corals documented for the U.S.
    [Show full text]
  • Volume 2. Animals
    AC20 Doc. 8.5 Annex (English only/Seulement en anglais/Únicamente en inglés) REVIEW OF SIGNIFICANT TRADE ANALYSIS OF TRADE TRENDS WITH NOTES ON THE CONSERVATION STATUS OF SELECTED SPECIES Volume 2. Animals Prepared for the CITES Animals Committee, CITES Secretariat by the United Nations Environment Programme World Conservation Monitoring Centre JANUARY 2004 AC20 Doc. 8.5 – p. 3 Prepared and produced by: UNEP World Conservation Monitoring Centre, Cambridge, UK UNEP WORLD CONSERVATION MONITORING CENTRE (UNEP-WCMC) www.unep-wcmc.org The UNEP World Conservation Monitoring Centre is the biodiversity assessment and policy implementation arm of the United Nations Environment Programme, the world’s foremost intergovernmental environmental organisation. UNEP-WCMC aims to help decision-makers recognise the value of biodiversity to people everywhere, and to apply this knowledge to all that they do. The Centre’s challenge is to transform complex data into policy-relevant information, to build tools and systems for analysis and integration, and to support the needs of nations and the international community as they engage in joint programmes of action. UNEP-WCMC provides objective, scientifically rigorous products and services that include ecosystem assessments, support for implementation of environmental agreements, regional and global biodiversity information, research on threats and impacts, and development of future scenarios for the living world. Prepared for: The CITES Secretariat, Geneva A contribution to UNEP - The United Nations Environment Programme Printed by: UNEP World Conservation Monitoring Centre 219 Huntingdon Road, Cambridge CB3 0DL, UK © Copyright: UNEP World Conservation Monitoring Centre/CITES Secretariat The contents of this report do not necessarily reflect the views or policies of UNEP or contributory organisations.
    [Show full text]
  • Voestalpine Essential Fish Habitat Assessment for PSD Greenhouse Gas Permit
    Essential Fish Habitat Assessment: Texas Project Site voestalpine Stahl GmbH San Patricio County, Texas January 31, 2013 www.erm.com voestalpine Stahl GmbH Essential Fish Habitat Assessment: Texas Project Site January 31, 2013 Project No. 0172451 San Patricio County, Texas Alicia Smith Partner-in-Charge Graham Donaldson Project Manager Travis Wycoff Project Consultant Environmental Resources Management 15810 Park Ten Place, Suite 300 Houston, Texas 77084-5140 T: 281-600-1000 F: 281-600-1001 Texas Registered Engineering Firm F-2393 TABLE OF CONTENTS LIST OF ACRONYMS IV EXECUTIVE SUMMARY VI 1.0 INTRODUCTION 1 1.1 PROPOSED ACTION 1 1.2 AGENCY REGULATIONS 1 1.2.1 Magnuson-Stevens Fishery Conservation and Management Act 1 1.2.1 Essential Fish Habitat Defined 2 2.0 PROJECT DESCRIPTION 4 2.1 PROJECT SCHEDULE 4 2.2 PROJECT LOCATION 4 2.3 SITE DESCRIPTION 5 2.4 SITE HISTORY 7 2.5 EMISSIONS CONTROLS 8 2.6 NOISE 9 2.7 DUST 10 2.8 WATER AND WASTEWATER 10 2.8.1 Water Sourcing and Water Rights 11 2.8.2 Wastewater Discharge 13 3.0 IDENTIFICATION OF THE ACTION AREA 15 3.1 ACTION AREA DEFINED 15 3.2 ACTION AREA DELINEATION METHODOLOGY AND RESULTS 16 3.2.1 Significant Impact Level Dispersion Modeling 16 3.2.2 Other Contaminants 17 4.0 ESSENTIAL FISH HABITAT IN THE VICINITY OF THE PROJECT 19 4.1 SPECIES OF PARTICULAR CONCERN 19 4.1.1 Brown Shrimp 19 4.1.2 Gray Snapper 20 4.1.3 Pink Shrimp 20 4.1.4 Red Drum 20 4.1.5 Spanish Mackerel 21 4.1.6 White Shrimp 21 4.2 HABITAT AREAS OF PARTICULAR CONCERN 22 5.0 ENVIRONMENTAL BASELINE CONDITIONS AND EFFECTS ANALYSIS
    [Show full text]
  • Revision of the Antipatharia (Cnidaria: Anthozoa)
    ZM 75 343-370 | 17 (opresko) 12-01-2007 07:55 Page 343 Revision of the Antipatharia (Cnidaria: Anthozoa). Part I. Establishment of a new family, Myriopathidae D.M. Opresko Opresko, D.M. Revision of the Antipatharia (Cnidaria: Anthozoa). Part I. Establishment of a new fami- ly, Myriopathidae. Zool. Med. Leiden 75 (17), 24.xii.2001: 343-370, figs. 1-18.— ISSN 0024-0672. Dennis M. Opresko, Life Sciences Division, Oak Ridge National Laboratory, 1060 Commerce Park, Oak Ridge, TN 37830, U.S.A. (e-mail: [email protected]). Key words: Cnidaria; Anthozoa: Antipatharia; Myriopathidae fam. nov.; Myriopathes gen. nov.; Cupressopathes gen. nov.; Plumapathes gen. nov.; Antipathella Brook; Tanacetipathes Opresko. A new family of antipatharian corals, Myriopathidae (Cnidaria: Anthozoa: Antipatharia), is estab- lished for Antipathes myriophylla Pallas and related species. The family is characterized by polyps 0.5 to 1.0 mm in transverse diameter; short tentacles with a rounded tip; acute, conical to blade-like spines up to 0.3 mm tall on the smallest branchlets or pinnules; and cylindrical, simple, forked or antler-like spines on the larger branches and stem. Genera are differentiated on the basis of morphological fea- tures of the corallum. Myriopathes gen. nov., type species Antipathes myriophylla Pallas, has two rows of primary pinnules, and uniserially arranged secondary pinnules. Tanacetipathes Opresko, type species T. tanacetum (Pourtalès), has bottle-brush pinnulation with four to six rows of primary pinnules and one or more orders of uniserial (sometimes biserial) subpinnules. Cupressopathes gen. nov., type species Gorgonia abies Linnaeus, has bottle-brush pinnulation with four very irregular, or quasi-spiral rows of primary pinnules and uniserial, bilateral, or irregularly arranged higher order pinnules.
    [Show full text]
  • III. Black Coral Fishery Management
    An Update on Recent Research and Management of Hawaiian Black Corals Chapter 6 in The State of Deep‐Sea Coral and Sponge Ecosystems of the United States Report Recommended citation: Wagner D, Opresko DM, Montgomery AD, Parrish FA (2017) An Update on Recent Research and Management of Hawaiian Black Corals. In: Hourigan TF, Etnoyer, PJ, Cairns, SD (eds.). The State of Deep‐Sea Coral and Sponge Ecosystems of the United States. NOAA Technical Memorandum NMFS‐OHC‐4, Silver Spring, MD. 44 p. Available online: http://deepseacoraldata.noaa.gov/library. Black coral Bathypathes on a rocky ridge crest of Johnston Atoll. Courtesy of the NOAA Office of Ocean Exploration and Research. RECENT RESEARCH & MANAGEMENT OF HAWAIIAN BLACK CORALS • • • AN UPDATE ON RECENT RESEARCH AND MANAGEMENT Daniel Wagner1*, Dennis M. OF HAWAIIAN Opresko2, Anthony D. Montgomery3, BLACK CORALS and Frank A. Parrish4 • • • 1 NOAA Papahānaumokuākea I. Introduction Marine National Monument Antipatharians, commonly known as black corals, are a Honolulu, HI little studied order of anthozoan hexacorals that currently encompasses over 235 described species (Cairns 2007, Daly (current affiliation: JHT, Inc., et al. 2007, Bo 2008). Black corals occur worldwide in all NOAA National Centers of oceans from polar to tropical regions, and have a wide Coastal Ocean Science depth distribution ranging from 2-8,600 m (reviewed by Charleston, SC) Wagner et al. 2012a). Despite this wide bathymetric range, * Corresponding Author: black corals are primarily found in deeper waters below [email protected] the photic zone, with over 75% of known species occurring exclusively below 50 m (Cairns 2007). At these depths, 2 National Museum of antipatharians are often abundant and dominant faunal Natural History, Smithsonian components, and create habitat for a myriad of associated Institution, Washington DC organisms (reviewed by Wagner et al.
    [Show full text]
  • CNIDARIA Corals, Medusae, Hydroids, Myxozoans
    FOUR Phylum CNIDARIA corals, medusae, hydroids, myxozoans STEPHEN D. CAIRNS, LISA-ANN GERSHWIN, FRED J. BROOK, PHILIP PUGH, ELLIOT W. Dawson, OscaR OcaÑA V., WILLEM VERvooRT, GARY WILLIAMS, JEANETTE E. Watson, DENNIS M. OPREsko, PETER SCHUCHERT, P. MICHAEL HINE, DENNIS P. GORDON, HAMISH J. CAMPBELL, ANTHONY J. WRIGHT, JUAN A. SÁNCHEZ, DAPHNE G. FAUTIN his ancient phylum of mostly marine organisms is best known for its contribution to geomorphological features, forming thousands of square Tkilometres of coral reefs in warm tropical waters. Their fossil remains contribute to some limestones. Cnidarians are also significant components of the plankton, where large medusae – popularly called jellyfish – and colonial forms like Portuguese man-of-war and stringy siphonophores prey on other organisms including small fish. Some of these species are justly feared by humans for their stings, which in some cases can be fatal. Certainly, most New Zealanders will have encountered cnidarians when rambling along beaches and fossicking in rock pools where sea anemones and diminutive bushy hydroids abound. In New Zealand’s fiords and in deeper water on seamounts, black corals and branching gorgonians can form veritable trees five metres high or more. In contrast, inland inhabitants of continental landmasses who have never, or rarely, seen an ocean or visited a seashore can hardly be impressed with the Cnidaria as a phylum – freshwater cnidarians are relatively few, restricted to tiny hydras, the branching hydroid Cordylophora, and rare medusae. Worldwide, there are about 10,000 described species, with perhaps half as many again undescribed. All cnidarians have nettle cells known as nematocysts (or cnidae – from the Greek, knide, a nettle), extraordinarily complex structures that are effectively invaginated coiled tubes within a cell.
    [Show full text]
  • Florida Keys Species List
    FKNMS Species List A B C D E F G H I J K L M N O P Q R S T 1 Marine and Terrestrial Species of the Florida Keys 2 Phylum Subphylum Class Subclass Order Suborder Infraorder Superfamily Family Scientific Name Common Name Notes 3 1 Porifera (Sponges) Demospongia Dictyoceratida Spongiidae Euryspongia rosea species from G.P. Schmahl, BNP survey 4 2 Fasciospongia cerebriformis species from G.P. Schmahl, BNP survey 5 3 Hippospongia gossypina Velvet sponge 6 4 Hippospongia lachne Sheepswool sponge 7 5 Oligoceras violacea Tortugas survey, Wheaton list 8 6 Spongia barbara Yellow sponge 9 7 Spongia graminea Glove sponge 10 8 Spongia obscura Grass sponge 11 9 Spongia sterea Wire sponge 12 10 Irciniidae Ircinia campana Vase sponge 13 11 Ircinia felix Stinker sponge 14 12 Ircinia cf. Ramosa species from G.P. Schmahl, BNP survey 15 13 Ircinia strobilina Black-ball sponge 16 14 Smenospongia aurea species from G.P. Schmahl, BNP survey, Tortugas survey, Wheaton list 17 15 Thorecta horridus recorded from Keys by Wiedenmayer 18 16 Dendroceratida Dysideidae Dysidea etheria species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 19 17 Dysidea fragilis species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 20 18 Dysidea janiae species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 21 19 Dysidea variabilis species from G.P. Schmahl, BNP survey 22 20 Verongida Druinellidae Pseudoceratina crassa Branching tube sponge 23 21 Aplysinidae Aplysina archeri species from G.P. Schmahl, BNP survey 24 22 Aplysina cauliformis Row pore rope sponge 25 23 Aplysina fistularis Yellow tube sponge 26 24 Aplysina lacunosa 27 25 Verongula rigida Pitted sponge 28 26 Darwinellidae Aplysilla sulfurea species from G.P.
    [Show full text]