Symposium 20084Th ISDSC Deepsea Coral
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National Monitoring Program for Biodiversity and Non-Indigenous Species in Egypt
UNITED NATIONS ENVIRONMENT PROGRAM MEDITERRANEAN ACTION PLAN REGIONAL ACTIVITY CENTRE FOR SPECIALLY PROTECTED AREAS National monitoring program for biodiversity and non-indigenous species in Egypt PROF. MOUSTAFA M. FOUDA April 2017 1 Study required and financed by: Regional Activity Centre for Specially Protected Areas Boulevard du Leader Yasser Arafat BP 337 1080 Tunis Cedex – Tunisie Responsible of the study: Mehdi Aissi, EcApMEDII Programme officer In charge of the study: Prof. Moustafa M. Fouda Mr. Mohamed Said Abdelwarith Mr. Mahmoud Fawzy Kamel Ministry of Environment, Egyptian Environmental Affairs Agency (EEAA) With the participation of: Name, qualification and original institution of all the participants in the study (field mission or participation of national institutions) 2 TABLE OF CONTENTS page Acknowledgements 4 Preamble 5 Chapter 1: Introduction 9 Chapter 2: Institutional and regulatory aspects 40 Chapter 3: Scientific Aspects 49 Chapter 4: Development of monitoring program 59 Chapter 5: Existing Monitoring Program in Egypt 91 1. Monitoring program for habitat mapping 103 2. Marine MAMMALS monitoring program 109 3. Marine Turtles Monitoring Program 115 4. Monitoring Program for Seabirds 118 5. Non-Indigenous Species Monitoring Program 123 Chapter 6: Implementation / Operational Plan 131 Selected References 133 Annexes 143 3 AKNOWLEGEMENTS We would like to thank RAC/ SPA and EU for providing financial and technical assistances to prepare this monitoring programme. The preparation of this programme was the result of several contacts and interviews with many stakeholders from Government, research institutions, NGOs and fishermen. The author would like to express thanks to all for their support. In addition; we would like to acknowledge all participants who attended the workshop and represented the following institutions: 1. -
The Coral Trait Database, a Curated Database of Trait Information for Coral Species from the Global Oceans
www.nature.com/scientificdata OPEN The Coral Trait Database, a curated SUBJECT CATEGORIES » Community ecology database of trait information for » Marine biology » Biodiversity coral species from the global oceans » Biogeography 1 2 3 2 4 Joshua S. Madin , Kristen D. Anderson , Magnus Heide Andreasen , Tom C.L. Bridge , , » Coral reefs 5 2 6 7 1 1 Stephen D. Cairns , Sean R. Connolly , , Emily S. Darling , Marcela Diaz , Daniel S. Falster , 8 8 2 6 9 3 Erik C. Franklin , Ruth D. Gates , Mia O. Hoogenboom , , Danwei Huang , Sally A. Keith , 1 2 2 4 10 Matthew A. Kosnik , Chao-Yang Kuo , Janice M. Lough , , Catherine E. Lovelock , 1 1 1 11 12 13 Osmar Luiz , Julieta Martinelli , Toni Mizerek , John M. Pandolfi , Xavier Pochon , , 2 8 2 14 Morgan S. Pratchett , Hollie M. Putnam , T. Edward Roberts , Michael Stat , 15 16 2 Carden C. Wallace , Elizabeth Widman & Andrew H. Baird Received: 06 October 2015 28 2016 Accepted: January Trait-based approaches advance ecological and evolutionary research because traits provide a strong link to Published: 29 March 2016 an organism’s function and fitness. Trait-based research might lead to a deeper understanding of the functions of, and services provided by, ecosystems, thereby improving management, which is vital in the current era of rapid environmental change. Coral reef scientists have long collected trait data for corals; however, these are difficult to access and often under-utilized in addressing large-scale questions. We present the Coral Trait Database initiative that aims to bring together physiological, morphological, ecological, phylogenetic and biogeographic trait information into a single repository. -
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. -
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. -
Crustaceans from Antipatharians on Banks of the Northwestern Gulf of Mexico
CORE Metadata, citation and similar papers at core.ac.uk Provided by ZENODO A peer-reviewed open-access journal ZooKeys 457: 45–54Crustaceans (2014) from antipatharians on banks of the northwestern Gulf of Mexico 45 doi: 10.3897/zookeys.457.6280 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Crustaceans from antipatharians on banks of the northwestern Gulf of Mexico Mary K. Wicksten1, Marissa F. Nuttall2, Emma L. Hickerson2 1 Biology, Texas A&M University, College Station Texas U.S.A. 77843-3258 2 Flower Gardens Banks Natio- nal Marine Sanctuary, 4700 Avenue U, Galveston, Texas 77551 U.S.A. Corresponding author: Mary K. Wicksten ([email protected]) Academic editor: I.S. Wehrtmann | Received 19 September 2013 | Accepted 13 January 2014 | Published 25 November 2014 http://zoobank.org/AFC34B87-FAED-44B8-BD24-14B0604259AB Citation: Wicksten MK, Nuttall MF, Hickerson EL (2014) Crustaceans from antipatharians on banks of the northwestern Gulf of Mexico. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 45–54. doi: 10.3897/zookeys.457.6280 Abstract The stalked barnacle Oxynaspis gracilis, the chirostylid squat lobster Uroptychus sp., and the caridean shrimps Periclimenes cf. antipathophilus and Pseudopontonides principis have been collected at 68–124 m by a remotely operated vehicle (ROV) on banks in the northern Gulf of Mexico. These species inhabited six species of antipatharian hosts. Pseudopontonides principis, O. gracilis, and U. sp. were not confined to a single host species. Except for O. -
Symbionts and Environmental Factors Related to Deep-Sea Coral Size and Health
Symbionts and environmental factors related to deep-sea coral size and health Erin Malsbury, University of Georgia Mentor: Linda Kuhnz Summer 2018 Keywords: deep-sea coral, epibionts, symbionts, ecology, Sur Ridge, white polyps ABSTRACT We analyzed video footage from a remotely operated vehicle to estimate the size, environmental variation, and epibiont community of three types of deep-sea corals (class Anthozoa) at Sur Ridge off the coast of central California. For all three of the corals, Keratoisis, Isidella tentaculum, and Paragorgia arborea, species type was correlated with the number of epibionts on the coral. Paragorgia arborea had the highest average number of symbionts, followed by Keratoisis. Epibionts were identified to the lowest possible taxonomic level and categorized as predators or commensalists. Around twice as many Keratoisis were found with predators as Isidella tentaculum, while no predators were found on Paragorgia arborea. Corals were also measured from photos and divided into size classes for each type based on natural breaks. The northern sites of the mound supported larger Keratoisis and Isidella tentaculum than the southern portion, but there was no relationship between size and location for Paragorgia arborea. The northern sites of Sur Ridge were also the only place white polyps were found. These polyps were seen mostly on Keratoisis, but were occasionally found on the skeletons of Isidella tentaculum and even Lillipathes, an entirely separate subclass of corals from Keratoisis. Overall, although coral size appears to be impacted by 1 environmental variables and location for Keratoisis and Isidella tentaculum, the presence of symbionts did not appear to correlate with coral size for any of the coral types. -
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. -
Author's Accepted Manuscript
Author’s Accepted Manuscript This is the accepted version of the following article: Rakka, M., Bilan, M., Godinho, A., Movilla, J., Orejas, C., & Carreiro-Silva, M. (2019). First description of polyp bailout in cold-water octocorals under aquaria maintenance. Coral Reefs, 38(1), 15-20, which has been published in final form at https://doi.org/10.1007/s00338-018-01760- x. This article may be used for non-commercial purposes in accordance with Springer Terms and Conditions for Use of Self-Archived Versions 1 First description of polyp bail-out in cold-water octocorals under aquaria maintenance Maria Rakka1,2,3, Meri Bilan1,2,3, Antonio Godinho1,2,3,Juancho Movilla4,5, Covadonga Orejas4, Marina Carreiro-Silva1,2,3 1 MARE – Marine and Environmental Sciences Centre and Centre of the Institute of Marine Research 2 IMAR – University of the Azores, Rua Frederico Machado 4, 9901-862 Horta, Portugal 3 OKEANOS Research Unit, Faculty of Science and Technology, University of the Azores, 9901-862, Horta, Portugal 4 Instituto Español de Oceanografía, Centro Oceanográfico de Baleares, Moll de Ponent s/n, 07015 Palma, Spain 5 Instituto de Ciencias del Mar (ICM-CSIC). Passeig Maritim de la Barceloneta 37-49, 08003 Barcelona, Spain Corresponding author: Maria Rakka, [email protected], +351915407062 2 Abstract Cnidarians, characterized by high levels of plasticity, exhibit remarkable mechanisms to withstand or escape unfavourable conditions including reverse development which describes processes of transformation of adult stages into early developmental stages with higher mobility. Polyp bail-out is a stress-escape response common among scleractinian species, consisting of massive detachment of live polyps and subsequent death of the mother colony. -
Guide to the Identification of Precious and Semi-Precious Corals in Commercial Trade
'l'llA FFIC YvALE ,.._,..---...- guide to the identification of precious and semi-precious corals in commercial trade Ernest W.T. Cooper, Susan J. Torntore, Angela S.M. Leung, Tanya Shadbolt and Carolyn Dawe September 2011 © 2011 World Wildlife Fund and TRAFFIC. All rights reserved. ISBN 978-0-9693730-3-2 Reproduction and distribution for resale by any means photographic or mechanical, including photocopying, recording, taping or information storage and retrieval systems of any parts of this book, illustrations or texts is prohibited without prior written consent from World Wildlife Fund (WWF). Reproduction for CITES enforcement or educational and other non-commercial purposes by CITES Authorities and the CITES Secretariat is authorized without prior written permission, provided the source is fully acknowledged. Any reproduction, in full or in part, of this publication must credit WWF and TRAFFIC North America. The views of the authors expressed in this publication do not necessarily reflect those of the TRAFFIC network, WWF, or the International Union for Conservation of Nature (IUCN). The designation of geographical entities in this publication and the presentation of the material do not imply the expression of any opinion whatsoever on the part of WWF, TRAFFIC, or IUCN concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. The TRAFFIC symbol copyright and Registered Trademark ownership are held by WWF. TRAFFIC is a joint program of WWF and IUCN. Suggested citation: Cooper, E.W.T., Torntore, S.J., Leung, A.S.M, Shadbolt, T. and Dawe, C. -
The Growth History of a Shallow Inshore Lophelia Pertusa Reef
Growth of North-East Atlantic Cold-Water Coral Reefs and Mounds during the Holocene: A High Resolution U-Series and 14C Chronology Mélanie Douarin1, Mary Elliot1, Stephen R. Noble2, Daniel Sinclair3, Lea- Anne Henry4, David Long5, Steven G. Moreton6,J. Murray Roberts4,7,8 1: School of Geosciences, The University of Edinburgh, Grant Institute, The King’s Buildings, West Mains Road, Edinburgh, Scotland, EH9 3JW, UK; [email protected] 2: NERC Isotope Geosciences Laboratory, British Geological Survey, Keyworth, Nottingham, England, NG12 5GG, UK 3: Marine Biogeochemistry & Paleoceanography Group, Institute of Marine and Coastal Sciences, Rutgers University, 71 Dudley Road, New Brunswick, NJ 08901-8525, USA 4: Centre for Marine Biodiversity & Biotechnology, School of Life Sciences, Heriot- Watt University, Edinburgh, Scotland, EH14 4AS, UK 5: British Geological Survey, West Mains Road, Edinburgh, Scotland, EH9 3LA, UK 6: NERC Radiocarbon Facility (Environment), Scottish Enterprise Technology Park, Rankine Avenue, East Kilbride, Glasgow, Scotland, G75 0QF, UK 7: Scottish Association for Marine Science, Scottish Marine Institute, Oban, Argyll, PA37 1QA, UK 8: Center for Marine Science, University of North Carolina Wilmington, 601 S. College Road, Wilmington, NC 28403-5928, USA 1. Abstract We investigate the Holocene growth history of the Mingulay Reef Complex, a seascape of inshore cold-water coral reefs off western Scotland, using U-series dating of 34 downcore and radiocarbon dating of 21 superficial corals. Both chronologies reveal that the reef framework-forming scleractinian coral Lophelia pertusa shows episodic occurrence during the late Holocene. Downcore U-series dating revealed unprecedented reef growth rates of up to 12 mm a-1 with a mean rate of 3 – 4 mm a-1. -
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