A Possible Method for Improving the Conservation Status of a Ellisella
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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. -
In the Long Island and It's Adjacent Areas in Middle Andaman, India
Indian Journal of Geo Marine Sciences Vol. 47 (01), January 2018, pp. 96-102 Diversity and distribution of gorgonians (Octocorallia) in the Long Island and it’s adjacent areas in Middle Andaman, India J. S. Yogesh Kumar1*, S. Geetha2, C. Raghunathan3 & R. Sornaraj2 1Marine Aquarium and Regional Centre, Zoological Survey of India, (Ministry of Environment, Forest and Climate Change), Government of India, Digha – 721428, West Bengal, India. 2Research Department of Zoology, Kamaraj College (Manonmaniam Sundaranar University), Thoothukudi – 628003, Tamil Nadu, India. 3Zoological Survey of India (Ministry of Environment, Forest and Climate Change), Government of India, M Block, New Alipore, Kolkata - 700 053,West Bengal, India. [E.mail: [email protected] ] Received 05 November 2015 ; revised 17 November 2016 The diversity and distribution of gorgonian were assessed at seven sites at Long Island and it’s adjusting areas in Middle Andaman during 2013 to 2015. A total of 28 species of gorgonians are reported in shallow reef areas. Maximum life form was observed in Guaiter Island and Minimum in Headlamp Patch. A significant positive correlation was observed between the Islands, the species diversity was high for the genera Junceella, Subergorgia and Ellisella. Principal Component Analysis also supported for this three genes. [Keywords: Diversity, Gorgonian, Octocoral, Long Island, Middle Andaman, Andaman and Nicobar, India] Introduction The gorgonians popularly called as sea In India, the study on gorgonians fans and sea whips are marine sessile taxonomy initiated by Thomson and coelenterates with colonial skeleton and living Henderson15,16 and 50 species were reported of polyps1. They are exceptionally productive and a which 26 species were new from oyster banks of valuable natural asset. -
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. -
The Global Trade in Marine Ornamental Species
From Ocean to Aquarium The global trade in marine ornamental species Colette Wabnitz, Michelle Taylor, Edmund Green and Tries Razak From Ocean to Aquarium The global trade in marine ornamental species Colette Wabnitz, Michelle Taylor, Edmund Green and Tries Razak ACKNOWLEDGEMENTS UNEP World Conservation This report would not have been The authors would like to thank Helen Monitoring Centre possible without the participation of Corrigan for her help with the analyses 219 Huntingdon Road many colleagues from the Marine of CITES data, and Sarah Ferriss for Cambridge CB3 0DL, UK Aquarium Council, particularly assisting in assembling information Tel: +44 (0) 1223 277314 Aquilino A. Alvarez, Paul Holthus and and analysing Annex D and GMAD data Fax: +44 (0) 1223 277136 Peter Scott, and all trading companies on Hippocampus spp. We are grateful E-mail: [email protected] who made data available to us for to Neville Ash for reviewing and editing Website: www.unep-wcmc.org inclusion into GMAD. The kind earlier versions of the manuscript. Director: Mark Collins assistance of Akbar, John Brandt, Thanks also for additional John Caldwell, Lucy Conway, Emily comments to Katharina Fabricius, THE UNEP WORLD CONSERVATION Corcoran, Keith Davenport, John Daphné Fautin, Bert Hoeksema, Caroline MONITORING CENTRE is the biodiversity Dawes, MM Faugère et Gavand, Cédric Raymakers and Charles Veron; for assessment and policy implemen- Genevois, Thomas Jung, Peter Karn, providing reprints, to Alan Friedlander, tation arm of the United Nations Firoze Nathani, Manfred Menzel, Julie Hawkins, Sherry Larkin and Tom Environment Programme (UNEP), the Davide di Mohtarami, Edward Molou, Ogawa; and for providing the picture on world’s foremost intergovernmental environmental organization. -
Deep-Sea Coral Taxa in the U. S. Caribbean Region: Depth And
Deep‐Sea Coral Taxa in the U. S. Caribbean Region: Depth and Geographical Distribution By Stephen D. Cairns1 1. National Museum of Natural History, Smithsonian Institution, Washington, DC An update of the status of the azooxanthellate, heterotrophic coral species that occur predominantly deeper than 50 m in the U.S. Caribbean territories is not given in this volume because of lack of significant additional data. However, an updated list of deep‐sea coral species in Phylum Cnidaria, Classes Anthozoa and Hydrozoa, from the Caribbean region (Figure 1) is presented below. Details are provided on depth ranges and known geographic distributions within the region (Table 1). This list is adapted from Lutz & Ginsburg (2007, Appendix 8.1) in that it is restricted to the U. S. territories in the Caribbean, i.e., Puerto Rico, U. S. Virgin Islands, and Navassa Island, not the entire Caribbean and Bahamian region. Thus, this list is significantly shorter. The list has also been reordered alphabetically by family, rather than species, to be consistent with other regional lists in this volume, and authorship and publication dates have been added. Also, Antipathes americana is now properly assigned to the genus Stylopathes, and Stylaster profundus to the genus Stenohelia. Furthermore, many of the geographic ranges have been clarified and validated. Since 2007 there have been 20 species additions to the U.S. territories list (indicated with blue shading in the list), mostly due to unpublished specimens from NMNH collections. As a result of this update, there are now known to be: 12 species of Antipatharia, 45 species of Scleractinia, 47 species of Octocorallia (three with incomplete taxonomy), and 14 species of Stylasteridae, for a total of 118 species found in the relatively small geographic region of U. -
Decision IG.24/7 Strategies and Action Plans Under the Protocol
UNEP/MED IG.24/22 Page 372 Decision IG.24/7 Strategies and Action Plans under the Protocol concerning Specially Protected Areas and Biological Diversity in the Mediterranean, including the SAP BIO, the Strategy on Monk Seal, and the Action Plans concerning Marine Turtles, Cartilaginous Fishes and Marine Vegetation; Classification of Benthic Marine Habitat Types for the Mediterranean Region, and Reference List of Marine and Coastal Habitat Types in the Mediterranean The Contracting Parties to the Convention for the Protection of the Marine Environment and the Coastal Region of the Mediterranean and its Protocols at their 21st Meeting, Recalling the outcome document of the United Nations Conference on Sustainable Development, entitled “The future we want”, endorsed by the General Assembly in its resolution 66/288 of 27 July 2012, in particular those paragraphs relevant to biodiversity, Recalling also General Assembly resolution 70/1 of 25 September 2015, entitled “Transforming our world: the 2030 Agenda for Sustainable Development”, and acknowledging the importance of conservation, the sustainable use and management of biodiversity in achieving the Sustainable Development Goals, Recalling further the United Nations Environment Assembly resolutions UNEP/EA.4/Res.10 of 15 March 2019, entitled “Innovation on biodiversity and land degradation”, Bearing in mind the international community’s commitment expressed in the Ministerial Declaration of the United Nations Environment Assembly at its fourth session to implement sustainable ecosystems -
Deep-Sea Life Issue 14, January 2020 Cruise News E/V Nautilus Telepresence Exploration of the U.S
Deep-Sea Life Issue 14, January 2020 Welcome to the 14th edition of Deep-Sea Life (a little later than anticipated… such is life). As always there is bound to be something in here for everyone. Illustrated by stunning photography throughout, learn about the deep-water canyons of Lebanon, remote Pacific Island seamounts, deep coral habitats of the Caribbean Sea, Gulf of Mexico, Southeast USA and the North Atlantic (with good, bad and ugly news), first trials of BioCam 3D imaging technology (very clever stuff), new deep pelagic and benthic discoveries from the Bahamas, high-risk explorations under ice in the Arctic (with a spot of astrobiology thrown in), deep-sea fauna sensitivity assessments happening in the UK and a new photo ID guide for mesopelagic fish. Read about new projects to study unexplored areas of the Mid-Atlantic Ridge and Azores Plateau, plans to develop a water-column exploration programme, and assessment of effects of ice shelf collapse on faunal assemblages in the Antarctic. You may also be interested in ongoing projects to address and respond to governance issues and marine conservation. It’s all here folks! There are also reports from past meetings and workshops related to deep seabed mining, deep-water corals, deep-water sharks and rays and information about upcoming events in 2020. Glance over the many interesting new papers for 2019 you may have missed, the scientist profiles, job and publishing opportunities and the wanted section – please help your colleagues if you can. There are brief updates from the Deep- Ocean Stewardship Initiative and for the deep-sea ecologists amongst you, do browse the Deep-Sea Biology Society president’s letter. -
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. -
Record of Viminella Flagellum (Alcyonacea: Ellisellidae) in Italian
Marine Biodiversity Records, page 1 of 5. # Marine Biological Association of the United Kingdom, 2012 doi:10.1017/S1755267211000510; Vol. 5; e34; 2012 Published online Record of Viminella flagellum (Alcyonacea: Ellisellidae) in Italian waters (Mediterranean Sea) m. giusti1,m.bo2, g. bavestrello2, m. angiolillo1, e. salvati1 and s. canese1 1ISPRA (ex ICRAM), Via di Casalotti 300, 00166 Roma, Italy, 2Dipartimento di Scienze del Mare, Universita` Politecnica delle Marche, 60131 Ancona, Italy The occurrence of the whip coral Viminella flagellum in Italian waters (Strait of Sicily, Mediterranean Sea), is reported for the first time. The specimens were photographed and sampled at locations situated from 130 to 250 m depth on the north-eastern coasts of Pantelleria Island, by means of a remotely operated vehicle, during a research cruise carried out by ISPRA in May 2010 on-board of the RV ‘Astrea’. A description of the living colonies and other taxonomic characteristics is given. Our finding extends the known geographical distribution of this species in the Mediterranean Sea to the Strait of Sicily. Keywords: Viminella flagellum, mesophotic zone, ROV exploration, biogeography, Pantelleria Island Submitted 21 February 2011; accepted 6 April 2011 INTRODUCTION substrata arising from detritic bottoms. Viminella flagellum may form dense monospecific aggregations, but was also Viminella flagellum (Johnson, 1863) (family Ellisellidae) is a recorded in mixed assemblages with Callogorgia verticillata whip-like gorgonian characterized by unbranched colonies (Pallas, 1766), Eunicella verrucosa (Pallas, 1766) and several up to 3 m high and has been only uncommonly observed species of other sea fans, like Swiftia pallida Madsen, 1970, with one or a few side branches (Carpine & Grasshoff, 1975; Paramuricea macrospina (Koch, 1882), and E. -
Deep-Sea Coral Taxa in the U.S. Southeast Region: Depth and Geographic Distribution (V
Deep-Sea Coral Taxa in the U.S. Southeast Region: Depth and Geographic Distribution (v. 2020) by Thomas F. Hourigan1, Stephen D. Cairns2, John K. Reed3, and Steve W. Ross4 1. NOAA Deep Sea Coral Research and Technology Program, Office of Habitat Conservation, Silver Spring, MD 2. National Museum of Natural History, Smithsonian Institution, Washington, DC 3. Cooperative Institute of Ocean Exploration, Research, and Technology, Harbor Branch Oceanographic Institute, Florida Atlantic University, Fort Pierce, FL 4. Center for Marine Science, University of North Carolina, Wilmington This annex to the U.S. Southeast chapter in “The State of Deep-Sea Coral and Sponge Ecosystems in the United States” provides a list of deep-sea coral taxa in the Phylum Cnidaria, Classes Anthozoa and Hydrozoa, known to occur in U.S. waters from Cape Hatteras to the Florida Keys (Figure 1). Deep-sea corals are defined as azooxanthellate, heterotrophic coral species occurring in waters 50 meters deep or more. Details are provided on the vertical and geographic extent of each species (Table 1). This list is an update of the peer-reviewed 2017 list (Hourigan et al. 2017) and includes taxa recognized through 2019, including one newly described species. 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 family, genus, and species. Data sources (references) listed are those principally used to establish geographic and depth distribution. Figure 1. U.S. Southeast region delimiting the geographic boundaries considered in this work. The region extends from Cape Hatteras to the Florida Keys and includes the Jacksonville Lithoherms (JL), Blake Plateau (BP), Oculina Coral Mounds (OC), Miami Terrace (MT), Pourtalès Terrace (PT), Florida Straits (FS), and Agassiz/Tortugas Valleys (AT). -
The Rare, Giant Gorgonian Ellisella Paraplexauroides: Demographics and Conservation Concerns
Vol. 479: 127–141, 2013 MARINE ECOLOGY PROGRESS SERIES Published April 8 doi: 10.3354/meps10172 Mar Ecol Prog Ser FREEREE ACCESSCCESS The rare, giant gorgonian Ellisella para plexauroides : demographics and conservation concerns Manuel Maldonado1,*, María López-Acosta1, Luis Sánchez-Tocino2, Cèlia Sitjà1 1Department of Marine Ecology, Centro de Estudios Avanzados de Blanes (CSIC-CEAB), Acceso Cala St. Francesc 14, 17300 Blanes, Girona, Spain 2Department of Zoology, Universidad de Granada, Campus Fuentenueva s/n, 18071 Granada, Spain ABSTRACT: A striking occurrence of the gorgonian coral Ellisella paraplexauroides off the Chafarinas Islands (western Mediterranean) requires serious conservation attention owing to considerable damage initiated by small fishing operations. Although this gorgonian is among the largest Atlantic-Mediterranean invertebrates, its biology remains virtually unknown. The studied population, established within an area of regulated fishing, was in unusually shallow waters (12−32 m). Density averaged 0.5 colonies m−2 (max 5 m−2); colony volume averaged 48 ml (max 511 ml), height averaged 76 cm (max 167 cm), and number of branches averaged 16 (max 72). Allometric growth revealed increasing branching and thickening once colonies reached approxi- mately 60 cm in height. Size distribution suggested moderate to low recruitment. Three geo- graphic zones of fishing pressure (A−C) were semi-quantitatively identified, based on the activity of a small-scale fishing fleet: ‘A’ had the highest level of fishing pressure (frequent gillnetting, trolling lines, and occasional trawling); ‘B’ had the lowest level (occasional gillnetting and fishing lines), and ‘C’ an intermediate level. Most fishing gear was tangled in the gorgonians in zones A and C. -
(Anthozoa: Alcyonacea: Ellisellidae) in the Persian Gulf
Biodiversity Data Journal 7: e33089 doi: 10.3897/BDJ.7.e33089 Short Communications First record of Viminella sp. (Anthozoa: Alcyonacea: Ellisellidae) in the Persian Gulf Shemshad Shahbazi‡, Nasrin Sakhaei‡, Hossein Zolgharnein§, Catherine S McFadden| ‡ Department of Marine Biology, Khorramshahr University of Marine Science and Technology, Khorramshahr, Iran § Department of Marine Biology, Khorramshahr University of Marine Science and Technology, Khorramshahr, Iran | Department of Biology, Harvey Mudd College, Claremont, CA, United States of America Corresponding author: Shemshad Shahbazi ([email protected]) Academic editor: Danwei Huang Received: 14 Jan 2019 | Accepted: 01 Feb 2019 | Published: 18 Jun 2019 Citation: Shahbazi S, Sakhaei N, Zolgharnein H, McFadden C (2019) First record of Viminella sp. (Anthozoa: Alcyonacea: Ellisellidae) in the Persian Gulf. Biodiversity Data Journal 7: e33089. https://doi.org/10.3897/BDJ.7.e33089 Abstract This paper presents the first record of Viminella Gray 1870 from the Persian Gulf. This genus has a global distribution and its largest distribution is in the Indo-Pacific region. A single specimen was collected by a local fisherman from south Hengam Island (the north Persian Gulf) from 60-70 m depth. Colony morphology characteristics were examined by stereomicroscope and optical microscope. Descriptions of the colony and other taxonomic characteristics are provided. The colony is unbranched with a height of 12 cm and its basal diameter is approximately 1.63 mm. The sclerites of the coenenchyme comprise a variety of symmetrical double heads and capstan-like forms (0.05-0.11 mm). In the wall of calyces, slightly elongated double heads, capstans and spindles (about 0.08-0.19 mm) are present.