A Revision of the Ahermatypic Scleractinia of the Philippine Islands and Adjacent Waters, Part 1
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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. -
Biological Results of the Chatham Islands 1954 Expedition
ISSN 2538-1016; 29 NEW ZEALAND DEPARTMENT OF SCIENTIFIC AND INDUSTRIAL RESEARCH BULLETIN 139 (6) Biological Results of The Chatham Islands 1954 Expedition PART 6 Scleractinia BY DONALD F. SQUIRES New Zealand Oceanographic Institute Memoir No. 29 1964 This publication is the sixth part of the Department of Scientificand Industrial Research Bulletin 139, which records the Biological Results of the Chatham Islands 1954 Expedition. Parts already published are: Part 1. Crustacea, by R. K. Dell, N. S. Jones, and J. C. Yaldwyn. Part 2. Archibenthal and Littoral Echinoderms, by H. Barraclough Fell. Part 3. Polychaeta Errantia, by G. A. Knox. Part 4. Marine Mollusca, by R. K. Dell; Sipunculoidea, by S. J. Edmonds. Part 5. Porifera: Demospongiae, by Patricia R. Bergquist; Porifera: Keratosa, by Patricia R. Bergquist; Crustacea Isopoda: Bopyridae, by R. B. Pike; Crustacea Isopoda: Serolidae, by D. E. Hurley; Hydroida, by Patricia M. Ralph. Additional parts are in preparation. A "General Account" of the Expedition was published as N.Z. Department of Scientific and Industrial Research Bulletin No. 122 (1957). BIOLOGICAL RESULTS OF THE CHATHAM ISLANDS 1954 EXPEDITION PART 6-SCLERACTINIA This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ Photograph: G. A. Knox. The Sero/is bromleyana - Spatangus multispinus community on the sorting screen. Aberrant growth form of Flabellum knoxi is in the lower left(see also plate 1, figs. 4-6). The abundant tubes are those of Hya!inoecia tubicola, the large starfish is Zoroaster spinu!osus, the echinoids Parameretia multituberculata. -
Information Review for Protected Deep-Sea Coral Species in the New Zealand Region
INFORMATION REVIEW FOR PROTECTED DEEP-SEA CORAL SPECIES IN THE NEW ZEALAND REGION NIWA Client Report: WLG2006-85 November 2006 NIWA Project: DOC06307 INFORMATION REVIEW FOR PROTECTED DEEP-SEA CORAL SPECIES IN THE NEW ZEALAND REGION Authors Mireille Consalvey Kevin MacKay Di Tracey Prepared for Department of Conservation NIWA Client Report: WLG2006-85 November 2006 NIWA Project: DOC06307 National Institute of Water & Atmospheric Research Ltd 301 Evans Bay Parade, Greta Point, Wellington Private Bag 14901, Kilbirnie, Wellington, New Zealand Phone +64-4-386 0300, Fax +64-4-386 0574 www.niwa.co.nz © All rights reserved. This publication may not be reproduced or copied in any form without the permission of the client. Such permission is to be given only in accordance with the terms of the client's contract with NIWA. This copyright extends to all forms of copying and any storage of material in any kind of information retrieval system. Contents Executive Summary iv 1. Introduction 1 2. Corals 1 3. Habitat 3 4. Corals as a habitat 3 5. Major taxonomic groups of deep-sea corals in New Zealand 5 6. Distribution of deep-sea corals in the New Zealand region 9 7. Systematics of deep-sea corals in New Zealand 18 8. Reproduction and recruitment of deep-sea corals 20 9. Growth rates and deep-sea coral ageing 22 10. Fishing effects on deep-sea corals 24 11. Other threats to deep-sea corals 29 12. Ongoing research into deep-sea corals in New Zealand 29 13. Future science and challenges to deep-sea coral research in New Zealand 30 14. -
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. -
Biodiversity of the Kermadec Islands and Offshore Waters of the Kermadec Ridge: Report of a Coastal, Marine Mammal and Deep-Sea Survey (TAN1612)
Biodiversity of the Kermadec Islands and offshore waters of the Kermadec Ridge: report of a coastal, marine mammal and deep-sea survey (TAN1612) New Zealand Aquatic Environment and Biodiversity Report No. 179 Clark, M.R.; Trnski, T.; Constantine, R.; Aguirre, J.D.; Barker, J.; Betty, E.; Bowden, D.A.; Connell, A.; Duffy, C.; George, S.; Hannam, S.; Liggins, L..; Middleton, C.; Mills, S.; Pallentin, A.; Riekkola, L.; Sampey, A.; Sewell, M.; Spong, K.; Stewart, A.; Stewart, R.; Struthers, C.; van Oosterom, L. ISSN 1179-6480 (online) ISSN 1176-9440 (print) ISBN 978-1-77665-481-9 (online) ISBN 978-1-77665-482-6 (print) January 2017 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 websites at: http://www.mpi.govt.nz/news-resources/publications.aspx http://fs.fish.govt.nz go to Document library/Research reports © Crown Copyright - Ministry for Primary Industries TABLE OF CONTENTS EXECUTIVE SUMMARY 1 1. INTRODUCTION 3 1.1 Objectives: 3 1.2 Objective 1: Benthic offshore biodiversity 3 1.3 Objective 2: Marine mammal research 4 1.4 Objective 3: Coastal biodiversity and connectivity 5 2. METHODS 5 2.1 Survey area 5 2.2 Survey design 6 Offshore Biodiversity 6 Marine mammal sampling 8 Coastal survey 8 Station recording 8 2.3 Sampling operations 8 Multibeam mapping 8 Photographic transect survey 9 Fish and Invertebrate sampling 9 Plankton sampling 11 Catch processing 11 Environmental sampling 12 Marine mammal sampling 12 Dive sampling operations 12 Outreach 13 3. -
DEEP SEA LEBANON RESULTS of the 2016 EXPEDITION EXPLORING SUBMARINE CANYONS Towards Deep-Sea Conservation in Lebanon Project
DEEP SEA LEBANON RESULTS OF THE 2016 EXPEDITION EXPLORING SUBMARINE CANYONS Towards Deep-Sea Conservation in Lebanon Project March 2018 DEEP SEA LEBANON RESULTS OF THE 2016 EXPEDITION EXPLORING SUBMARINE CANYONS Towards Deep-Sea Conservation in Lebanon Project Citation: Aguilar, R., García, S., Perry, A.L., Alvarez, H., Blanco, J., Bitar, G. 2018. 2016 Deep-sea Lebanon Expedition: Exploring Submarine Canyons. Oceana, Madrid. 94 p. DOI: 10.31230/osf.io/34cb9 Based on an official request from Lebanon’s Ministry of Environment back in 2013, Oceana has planned and carried out an expedition to survey Lebanese deep-sea canyons and escarpments. Cover: Cerianthus membranaceus © OCEANA All photos are © OCEANA Index 06 Introduction 11 Methods 16 Results 44 Areas 12 Rov surveys 16 Habitat types 44 Tarablus/Batroun 14 Infaunal surveys 16 Coralligenous habitat 44 Jounieh 14 Oceanographic and rhodolith/maërl 45 St. George beds measurements 46 Beirut 19 Sandy bottoms 15 Data analyses 46 Sayniq 15 Collaborations 20 Sandy-muddy bottoms 20 Rocky bottoms 22 Canyon heads 22 Bathyal muds 24 Species 27 Fishes 29 Crustaceans 30 Echinoderms 31 Cnidarians 36 Sponges 38 Molluscs 40 Bryozoans 40 Brachiopods 42 Tunicates 42 Annelids 42 Foraminifera 42 Algae | Deep sea Lebanon OCEANA 47 Human 50 Discussion and 68 Annex 1 85 Annex 2 impacts conclusions 68 Table A1. List of 85 Methodology for 47 Marine litter 51 Main expedition species identified assesing relative 49 Fisheries findings 84 Table A2. List conservation interest of 49 Other observations 52 Key community of threatened types and their species identified survey areas ecological importanc 84 Figure A1. -
Cold-Water Corals Online Appendix: Recent Azooxanthellate Scleractinia
Cold-water Corals Online Appendix Phylogenetic list of 711 valid Recent azooxanthellate scleractinian species, with their junior synonyms and depth ranges Notes Type species of the genus indicated with an asterisk, valid species names in bold-type Eleven facultatively zooxanthellate species Taxa prefaced with a single square bracket are not valid species and thus are not counted Last revised September 2008 (Stephen D. Cairns) Suborder ASTROCOENIINA FAMILY POCILLOPORIDAE Gray, 1842 Madracis Milne Edwards & Haime, 1849 *asperula Milne Edwards & Haime, 1849 (facultative, H. Zibrowius, pers. comm..; 0-311 m) pharensis cf. pharensis (Heller, 1868) (facultative; 6-333 m) =?M. cf. pharensis sensu Cairns, 1991: 6 (Galápagos, 30-343 m) =?M. cf. pharensis sensu Cairns & Zibrowius, 1997: 67 (Banda Sea, 85-421 m) asanoi Yabe & Sugiyama, 1936 (110-183 m) =M. palaoensis Yabe & Sugiyama, 1936 kauaiensis Vaughan, 1907 (44-541 m) ?=singularis Rehberg, 1892 ?=interjecta Marenzeller, 1907 var. macrocalyx Vaughan, 1907 (160-260 m) hellana Milne Edwards & Haime, 1850 (46 m) myriaster (Milne Edwards & Haime, 1849) (37-1220 m) =Stylophora mirabilis Duchassaing & Michelotti, 1860 =Axohelia schrammii Pourtalès, 1874 brueggemanni (Ridley, 1881) (51-130 m) =M. scotiae Gardiner, 1913 profunda Zibrowius, 1980 (112-327 m) [sp. A =sensu Wells, 1954: 414 (Marshall I.) =cf. asperula, sensu Cairns, 1991: 5 (Galápagos, 46-64 m) =sensu Cairns & Keller, 1993:228 (SWIO, 62-160 m) =sensu Cairns, 1994: 36 (Japan, 46-110 m) =sensu Cairns & Zibrowius, 1997: 67 (Philippines, 124-208 m) Suborder FUNGIINA Superfamily FUNGIOIDEA Dana, 1846 FAMILY FUNGIACYATHIDAE Chevalier, 1987 Fungiacyathus (F.) Sars, 1872 *fragilis Sars, 1872 (200-2200 m) (not F. fragilis Keller, 1976 (junior homonym)) =Bathyactis hawaiiensis Vaughan, 1907 paliferus (Alcock, 1902) (69-823 m) =Bathyactis kikaiensis Yabe & Eguchi, 1942 (fossil) =F. -
Taxonomy and Phylogenetic Relationships of the Coral Genera Australomussa and Parascolymia (Scleractinia, Lobophylliidae)
Contributions to Zoology, 83 (3) 195-215 (2014) Taxonomy and phylogenetic relationships of the coral genera Australomussa and Parascolymia (Scleractinia, Lobophylliidae) Roberto Arrigoni1, 7, Zoe T. Richards2, Chaolun Allen Chen3, 4, Andrew H. Baird5, Francesca Benzoni1, 6 1 Dept. of Biotechnology and Biosciences, University of Milano-Bicocca, 20126, Milan, Italy 2 Aquatic Zoology, Western Australian Museum, 49 Kew Street, Welshpool, WA 6106, Australia 3Biodiversity Research Centre, Academia Sinica, Nangang, Taipei 115, Taiwan 4 Institute of Oceanography, National Taiwan University, Taipei 106, Taiwan 5 ARC Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, QLD 4811, Australia 6 Institut de Recherche pour le Développement, UMR227 Coreus2, 101 Promenade Roger Laroque, BP A5, 98848 Noumea Cedex, New Caledonia 7 E-mail: [email protected] Key words: COI, evolution, histone H3, Lobophyllia, Pacific Ocean, rDNA, Symphyllia, systematics, taxonomic revision Abstract Molecular phylogeny of P. rowleyensis and P. vitiensis . 209 Utility of the examined molecular markers ....................... 209 Novel micromorphological characters in combination with mo- Acknowledgements ...................................................................... 210 lecular studies have led to an extensive revision of the taxonomy References ...................................................................................... 210 and systematics of scleractinian corals. In the present work, we Appendix ....................................................................................... -
Patterns of Septal Biomineralization in Scleractinia Compared with Their 28S Rrna Phylogeny
PBlackwell Publishingatterns Ltd. of septal biomineralization in Scleractinia compared with their 28S rRNA phylogeny: a dual approach for a new taxonomic framework JEAN-PIERRE CUIF, GUILLAUME LECOINTRE, CHRISTINE PERRIN, ANNIE TILLIER & SIMON TILLIER Accepted: 2 December 2002 Cuif, J.-P., Lecointre, G., Perrin, C., Tillier, A. & Tillier, S. (2003). Patterns of septal bio- mineralization in Scleractinia compared with their 28S rRNA phylogeny: a dual approach for a new taxonomic framework. — Zoologica Scripta, 32, 459–473. A molecular phylogeny of the Scleractinia is reconstructed from approximately 700 nucleo- tides of the 5′end of the 28S rDNA obtained from 40 species. A comparison of molecular phylogenic trees with biomineralization patterns of coral septa suggests that at least five clades are corroborated by both types of data. Agaricidae and Dendrophylliidae are found to be monophyletic, that is supported by microstructural data. Conversely, Faviidae and Caryophyl- liidae are found to be paraphyletic: Cladocora should be excluded from the faviids, whereas Eusmilia should be excluded from the caryophylliids. The conclusion is also supported by the positions, sizes and shapes of centres of calcification. The traditional Guyniidae are diphyletic, corroborating Stolarski’s hypothesis ‘A’. Some results from our most parsimonious trees are not strongly statistically supported but corroborated by other molecular studies and micro- structural observations. For example, in the scleractinian phylogenetic tree, there are several lines of evidence (including those from our data) to distinguish a Faviidae–Mussidae lineage and a Dendrophylliidae–Agaricidae–Poritidae–Siderastreidae lineage. From a methodological standpoint, our results suggest that co-ordinated studies creating links between biomineralization patterns and molecular phylogeny may provide an efficient working approach for a re- examination of scleractinian classification. -
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. -
New Azooxanthellate Genus of Scleractinia (Flabellidae) from the Australian Cenozoic
Journal of Paleontology, page 1 of 10 Copyright © 2017, The Paleontological Society 0022-3360/16/0088-0906 doi: 10.1017/jpa.2016.83 New azooxanthellate genus of Scleractinia (Flabellidae) from the Australian Cenozoic Stephen D. Cairns Department of Invertebrate Zoology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560, USA 〈[email protected]〉 Abstract.—A new genus of flabellid scleractinian coral, Periplacotrochus, is described from the late Eocene to middle Miocene of Victoria, South Australia, and Tasmania. It differs from Placotrochus in having a pedicellate base, and from Flabellum in having a lamellar columella. Six previously described species are redescribed, illustrated, and reassigned to this genus (P. deltoideus Duncan, 1864, P. corniculatus Dennant, 1899, P. elongatus Duncan, 1864, P. pueblensis Dennant, 1903,P.inflectus Dennant, 1903, and P. magnus Dennant, 1904), and one new species is described: P. cudmorei. One species, Placotrochus elegans Tennison-Woods, 1878a, is considered as a nomen dubium. A key is provided to the seven species placed in this genus. Introduction According to Duncan (1864), the genus Flabellum could be considered mimetic to Truncatoflabellum, differing only in Duncan (1864) noted that there were ‘paired’ flabellid genera, or lacking transverse division. In the same way, Periplacotrochus maybe only groups of species, differing from one another by only could be considered mimetic to Flabellum, differing only in one character, such as the presence or absence of a lamellar having a lamellar columella. Likewise, Truncatoflabellum could columella. He called these ‘mimetic’ genera, or those that mimic be considered mimetic to Placotrochus, differing only in lacking one another, except for one character. -
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.