Deep-Water Octocorals (Anthozoa: Cnidaria) Collected from the Colombian Caribbean During ‘Macrofauna Explorations’ 1998-2002*
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Zootaxa, a New Genus of Soft Coral (Octocorallia: Alcyonacea: Clavulariidae)
Zootaxa 1219: 47–57 (2006) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 1219 Copyright © 2006 Magnolia Press ISSN 1175-5334 (online edition) A new genus of soft coral (Octocorallia: Alcyonacea: Clavulariidae) from Chile L.P. VAN OFWEGEN1, V. HÄUSSERMANN2 & G. FÖRSTERRA2 1Nationaal Natuurhistorisch Museum, P.O. Box 9517, 2300 RA Leiden, The Netherlands. E-mail: [email protected] 2Universidad Austral de Chile, Departamento de Biología Marina, Campus Isla Teja, Casilla 567, Valdivia, Chile. E-mail: [email protected], [email protected] Abstract Incrustatus comauensis n. gen. & n. sp. (Octocorallia: Clavulariidae) is described from Chile. It occurs in shallow water from Concepción to the southern fjord region. The genus forms stolons on mytilid shells and rocks, or encrusting sheets on Crepidula shells (Gastropoda), polychaete tubes, gorgonians, and other substrata. The sclerites of the new taxon are 8-radiates and derivatives of these. The polyps are unarmed or posses a few irregularly arranged spindles. The new genus is compared with another taxon that forms encrusting sheets or stolons. Key words: Coelenterata, Cnidaria, Octocorallia, Alcyonacea, Clavulariidae, benthos, Incrustatus, new genus, new species, Chile Introduction The shallow water soft coral fauna of the Chilean coast is still almost completely unknown. To date one stoloniferous species has been described from Chile, Clavularia magelhaenica Studer, 1878, from the Straits of Magellan. From 1997 onwards, Verena Häussermann and Günter Försterra investigated the anthozoan fauna of Chile, with a focus on the South Chilean fjord region, and collected many specimens. This soft coral collection includes several undescribed species of Alcyonium, a species of Renilla, and some possible clavulariids, among which was an as yet undescribed new genus that is the subject of this paper. -
A Mass Mortality of <I>Gorgonia Ventalina</I>
BULLETIN OF MARINE SCIENCE, 50(3): 522-526. 1992 A MASS MORTALITY OF GORGONIA VENT ALINA (CNIDARIA: GORGONIIDAE) IN THE SANTA MARTA AREA, CARIBBEAN COAST OF COLOMBIA Jaime Garzon-Ferreira and Sven Zea The steep, rocky shores of the Santa Marta area (including the Tayrona Natural Park) in the Colombian Caribbean (11012'N and 74°14'W to 11°18'N and 73°54'W) comprise more than 90 km of irregular shoreline (Fig. 1). Hard substrata continue below the sea surface usually down to a maximum depth of 30 m, supporting rich communities of reef associated organisms (Garzon-Ferreira and Cano, 1990). Gorgonaceans are common and can dominate the sessile biocoenosis at some sites. The sea fan, Gorgonia ventalina Linnaeus (Cnidaria, Gorgoniidae), was known as one of the most conspicuous and abundant of the 39 living species of gorgonaceans in the area (Botero, 1987a, 1987b; pers. observ.). In September 1988, one of us (J.G.-F.) started to dive intensively in the area to map marine communities, and noted the absence of live individuals of sea fans. By the end of 1990, J.G.-F. had surveyed most of the coast to a depth of 20-30 m, and was able to recognize the dramatic mortality suffered by sea fans around Santa Marta. This note documents this mass mortality, compares it with other similar events and discusses its possible date of occurrence and causes. There are a few reports of octocoral mass mortalities in the tropical western Atlantic, all of which involved mainly sea fans and occurred along the southern Caribbean during the 1980's (Fig. -
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. -
End-Permian Mass Extinction in the Oceans: an Ancient Analog for the Twenty-First Century?
EA40CH05-Payne ARI 23 March 2012 10:24 End-Permian Mass Extinction in the Oceans: An Ancient Analog for the Twenty-First Century? Jonathan L. Payne1 and Matthew E. Clapham2 1Department of Geological and Environmental Sciences, Stanford University, Stanford, California 94305; email: [email protected] 2Department of Earth and Planetary Sciences, University of California, Santa Cruz, California 95064; email: [email protected] Annu. Rev. Earth Planet. Sci. 2012. 40:89–111 Keywords First published online as a Review in Advance on ocean acidification, evolution, isotope geochemistry, volcanism, January 3, 2012 biodiversity The Annual Review of Earth and Planetary Sciences is online at earth.annualreviews.org Abstract This article’s doi: The greatest loss of biodiversity in the history of animal life occurred at the 10.1146/annurev-earth-042711-105329 end of the Permian Period (∼252 million years ago). This biotic catastro- Annu. Rev. Earth Planet. Sci. 2012.40:89-111. Downloaded from www.annualreviews.org Copyright c 2012 by Annual Reviews. phe coincided with an interval of widespread ocean anoxia and the eruption All rights reserved of one of Earth’s largest continental flood basalt provinces, the Siberian by Stanford University - Main Campus Robert Crown Law Library on 06/04/12. For personal use only. 0084-6597/12/0530-0089$20.00 Traps. Volatile release from basaltic magma and sedimentary strata dur- ing emplacement of the Siberian Traps can account for most end-Permian paleontological and geochemical observations. Climate change and, per- haps, destruction of the ozone layer can explain extinctions on land, whereas changes in ocean oxygen levels, CO2, pH, and temperature can account for extinction selectivity across marine animals. -
Coelenterata: Anthozoa), with Diagnoses of New Taxa
PROC. BIOL. SOC. WASH. 94(3), 1981, pp. 902-947 KEY TO THE GENERA OF OCTOCORALLIA EXCLUSIVE OF PENNATULACEA (COELENTERATA: ANTHOZOA), WITH DIAGNOSES OF NEW TAXA Frederick M. Bayer Abstract.—A serial key to the genera of Octocorallia exclusive of the Pennatulacea is presented. New taxa introduced are Olindagorgia, new genus for Pseudopterogorgia marcgravii Bayer; Nicaule, new genus for N. crucifera, new species; and Lytreia, new genus for Thesea plana Deich- mann. Ideogorgia is proposed as a replacement ñame for Dendrogorgia Simpson, 1910, not Duchassaing, 1870, and Helicogorgia for Hicksonella Simpson, December 1910, not Nutting, May 1910. A revised classification is provided. Introduction The key presented here was an essential outgrowth of work on a general revisión of the octocoral fauna of the western part of the Atlantic Ocean. The far-reaching zoogeographical affinities of this fauna made it impossible in the course of this study to ignore genera from any part of the world, and it soon became clear that many of them require redefinition according to modern taxonomic standards. Therefore, the type-species of as many genera as possible have been examined, often on the basis of original type material, and a fully illustrated generic revisión is in course of preparation as an essential first stage in the redescription of western Atlantic species. The key prepared to accompany this generic review has now reached a stage that would benefit from a broader and more objective testing under practical conditions than is possible in one laboratory. For this reason, and in order to make the results of this long-term study available, even in provisional form, not only to specialists but also to the growing number of ecologists, biochemists, and physiologists interested in octocorals, the key is now pre- sented in condensed form with minimal illustration. -
Gonian Eunicella Singularis (Esper, 1791) (Anthozoa Gorgoni - Idae) of Paloma Island, Algeria
Biodiversity Journal , 2019, 10 (3): 185–194 https://doi.org/ 10.31396/Biodiv.Jour.2019.10.3.185.194 Morphometric data and allometric relationships of the gor - gonian Eunicella singularis (Esper, 1791) (Anthozoa Gorgoni - idae) of Paloma Island, Algeria Mouloud Benabdi 1, Lalla A. T. Cherif-Louazani 1, Alae Eddine Belmahi 1, Samir Grimes 2, Yassine G.E. Khames 3, Billel Boufekane 3, Salim Mouffok 1 & Mohamed Bouderbala 1 1Laboratoire Réseau de Surveillance Environnementale, Faculté SNV, Université Oran1, Algeria 2École Nationale Supérieure des Sciences de la Mer et de l’Aménagement du Littoral Alger, Algeria 3Faculté des Sciences Biologiques, USTHB, Alger, Algeria *Corresponding author, email: [email protected] ABSTRACT The gorgonian Eunicella singularis (Esper, 1791) (Anthozoa Gorgoniidae) is abundant on rocky bottoms at Paloma Island (Algeria) in the south-western of the Mediterranean basin. In this study area, 150 gorgonian colonies of E. singularis were collected randomly using SCUBA diving and the following morphometric macro-features were measured (maximum height, maximum width, total branch length, rectangular surface area, height to width ratio and dry weight). Allometric growth was examined using the relationships between the dry weight and the five morphometric macro-features. The power equation of the simple allometry applied was y=ax b and the parameters of the linear regression a and b were estimated after the logarithmic transformation log (y)=log( a)+ b*log(x). The allometric relationships between the dry weight and the morphometric macro-features studied show that the growth of the gor - gonian E. singularis in the study area is correlated positively and significantly with the five macro-features and that both the macro-features total branch length and the maximum width are the most appropriate parameter applied to the gorgonian E. -
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. -
Table B – Subclass Octocorallia
Table B – Subclass Octocorallia BINOMEN ORDER SUBORDER FAMILY SUBFAMILY GENUS SPECIES SUBSPECIES COMN_NAMES AUTHORITY SYNONYMS #Records Acanella arbuscula Alcyonacea Calcaxonia Isididae n/a Acanella arbuscula n/a n/a n/a n/a 59 Acanthogorgia armata Alcyonacea Holaxonia Acanthogorgiidae n/a Acanthogorgia armata n/a n/a Verrill, 1878 n/a 95 Anthomastus agassizii Alcyonacea Alcyoniina Alcyoniidae n/a Anthomastus agassizii n/a n/a (Verrill, 1922) n/a 35 Anthomastus grandiflorus Alcyonacea Alcyoniina Alcyoniidae n/a Anthomastus grandiflorus n/a n/a Verrill, 1878 Anthomastus purpureus 37 Anthomastus sp. Alcyonacea Alcyoniina Alcyoniidae n/a Anthomastus sp. n/a n/a Verrill, 1878 n/a 1 Anthothela grandiflora Alcyonacea Scleraxonia Anthothelidae n/a Anthothela grandiflora n/a n/a (Sars, 1856) n/a 24 Capnella florida Alcyonacea n/a Nephtheidae n/a Capnella florida n/a n/a (Verrill, 1869) Eunephthya florida 44 Capnella glomerata Alcyonacea n/a Nephtheidae n/a Capnella glomerata n/a n/a (Verrill, 1869) Eunephthya glomerata 4 Chrysogorgia agassizii Alcyonacea Holaxonia Acanthogorgiidae Chrysogorgiidae Chrysogorgia agassizii n/a n/a (Verrill, 1883) n/a 2 Clavularia modesta Alcyonacea n/a Clavulariidae n/a Clavularia modesta n/a n/a (Verrill, 1987) n/a 6 Clavularia rudis Alcyonacea n/a Clavulariidae n/a Clavularia rudis n/a n/a (Verrill, 1922) n/a 1 Gersemia fruticosa Alcyonacea Alcyoniina Alcyoniidae n/a Gersemia fruticosa n/a n/a Marenzeller, 1877 n/a 3 Keratoisis flexibilis Alcyonacea Calcaxonia Isididae n/a Keratoisis flexibilis n/a n/a Pourtales, 1868 n/a 1 Lepidisis caryophyllia Alcyonacea n/a Isididae n/a Lepidisis caryophyllia n/a n/a Verrill, 1883 Lepidisis vitrea 13 Muriceides sp. -
Deep-Sea Origin and In-Situ Diversification of Chrysogorgiid Octocorals
Deep-Sea Origin and In-Situ Diversification of Chrysogorgiid Octocorals Eric Pante1*¤, Scott C. France1, Arnaud Couloux2, Corinne Cruaud2, Catherine S. McFadden3, Sarah Samadi4, Les Watling5,6 1 Department of Biology, University of Louisiana at Lafayette, Lafayette, Louisiana, United States of America, 2 GENOSCOPE, Centre National de Se´quenc¸age, Evry, France, 3 Department of Biology, Harvey Mudd College, Claremont, California, United States of America, 4 De´partement Syste´matique et Evolution, UMR 7138 UPMC-IRD-MNHN- CNRS (UR IRD 148), Muse´um national d’Histoire naturelle, Paris, France, 5 Department of Biology, University of Hawaii at Manoa, Honolulu, Hawaii, United States of America, 6 Darling Marine Center, University of Maine, Walpole, Maine, United States of America Abstract The diversity, ubiquity and prevalence in deep waters of the octocoral family Chrysogorgiidae Verrill, 1883 make it noteworthy as a model system to study radiation and diversification in the deep sea. Here we provide the first comprehensive phylogenetic analysis of the Chrysogorgiidae, and compare phylogeny and depth distribution. Phylogenetic relationships among 10 of 14 currently-described Chrysogorgiidae genera were inferred based on mitochondrial (mtMutS, cox1) and nuclear (18S) markers. Bathymetric distribution was estimated from multiple sources, including museum records, a literature review, and our own sampling records (985 stations, 2345 specimens). Genetic analyses suggest that the Chrysogorgiidae as currently described is a polyphyletic family. Shallow-water genera, and two of eight deep-water genera, appear more closely related to other octocoral families than to the remainder of the monophyletic, deep-water chrysogorgiid genera. Monophyletic chrysogorgiids are composed of strictly (Iridogorgia Verrill, 1883, Metallogorgia Versluys, 1902, Radicipes Stearns, 1883, Pseudochrysogorgia Pante & France, 2010) and predominantly (Chrysogorgia Duchassaing & Michelotti, 1864) deep-sea genera that diversified in situ. -
The Genetic Identity of Dinoflagellate Symbionts in Caribbean Octocorals
Coral Reefs (2004) 23: 465-472 DOI 10.1007/S00338-004-0408-8 REPORT Tamar L. Goulet • Mary Alice CofFroth The genetic identity of dinoflagellate symbionts in Caribbean octocorals Received: 2 September 2002 / Accepted: 20 December 2003 / Published online: 29 July 2004 © Springer-Verlag 2004 Abstract Many cnidarians (e.g., corals, octocorals, sea Introduction anemones) maintain a symbiosis with dinoflagellates (zooxanthellae). Zooxanthellae are grouped into The cornerstone of the coral reef ecosystem is the sym- clades, with studies focusing on scleractinian corals. biosis between cnidarians (e.g., corals, octocorals, sea We characterized zooxanthellae in 35 species of Caribbean octocorals. Most Caribbean octocoral spe- anemones) and unicellular dinoñagellates commonly called zooxanthellae. Studies of zooxanthella symbioses cies (88.6%) hosted clade B zooxanthellae, 8.6% have previously been hampered by the difficulty of hosted clade C, and one species (2.9%) hosted clades B and C. Erythropodium caribaeorum harbored clade identifying the algae. Past techniques relied on culturing and/or identifying zooxanthellae based on their free- C and a unique RFLP pattern, which, when se- swimming form (Trench 1997), antigenic features quenced, fell within clade C. Five octocoral species (Kinzie and Chee 1982), and cell architecture (Blank displayed no zooxanthella cladal variation with depth. 1987), among others. These techniques were time-con- Nine of the ten octocoral species sampled throughout suming, required a great deal of expertise, and resulted the Caribbean exhibited no regional zooxanthella cla- in the differentiation of only a small number of zoo- dal differences. The exception, Briareum asbestinum, xanthella species. Molecular techniques amplifying had some colonies from the Dry Tortugas exhibiting zooxanthella DNA encoding for the small and large the E. -
Phylogenetic Relationships Within Chrysogorgia (Alcyonacea
Phylogenetic Relationships Within Chrysogorgia (Alcyonacea: Octocorallia), a Morphologically Diverse Genus of Octocoral, Revealed Using a Target Enrichment Approach Candice Untiedt, Andrea Quattrini, Catherine Mcfadden, Phil Alderslade, Eric Pante, Christopher Burridge To cite this version: Candice Untiedt, Andrea Quattrini, Catherine Mcfadden, Phil Alderslade, Eric Pante, et al.. Phy- logenetic Relationships Within Chrysogorgia (Alcyonacea: Octocorallia), a Morphologically Diverse Genus of Octocoral, Revealed Using a Target Enrichment Approach. Frontiers in Marine Science, Frontiers Media, 2021, 7, 10.3389/fmars.2020.599984. hal-03154113 HAL Id: hal-03154113 https://hal.sorbonne-universite.fr/hal-03154113 Submitted on 27 Feb 2021 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. fmars-07-599984 January 11, 2021 Time: 10:55 # 1 ORIGINAL RESEARCH published: 12 January 2021 doi: 10.3389/fmars.2020.599984 Phylogenetic Relationships Within Chrysogorgia (Alcyonacea: Octocorallia), a Morphologically Diverse Genus of Octocoral, Revealed Using a Target Enrichment