Coral Reefs, Biodiversity, Distribution Patterns, Persian Gulf
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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. -
Taxonomic Checklist of CITES Listed Coral Species Part II
CoP16 Doc. 43.1 (Rev. 1) Annex 5.2 (English only / Únicamente en inglés / Seulement en anglais) Taxonomic Checklist of CITES listed Coral Species Part II CORAL SPECIES AND SYNONYMS CURRENTLY RECOGNIZED IN THE UNEP‐WCMC DATABASE 1. Scleractinia families Family Name Accepted Name Species Author Nomenclature Reference Synonyms ACROPORIDAE Acropora abrolhosensis Veron, 1985 Veron (2000) Madrepora crassa Milne Edwards & Haime, 1860; ACROPORIDAE Acropora abrotanoides (Lamarck, 1816) Veron (2000) Madrepora abrotanoides Lamarck, 1816; Acropora mangarevensis Vaughan, 1906 ACROPORIDAE Acropora aculeus (Dana, 1846) Veron (2000) Madrepora aculeus Dana, 1846 Madrepora acuminata Verrill, 1864; Madrepora diffusa ACROPORIDAE Acropora acuminata (Verrill, 1864) Veron (2000) Verrill, 1864; Acropora diffusa (Verrill, 1864); Madrepora nigra Brook, 1892 ACROPORIDAE Acropora akajimensis Veron, 1990 Veron (2000) Madrepora coronata Brook, 1892; Madrepora ACROPORIDAE Acropora anthocercis (Brook, 1893) Veron (2000) anthocercis Brook, 1893 ACROPORIDAE Acropora arabensis Hodgson & Carpenter, 1995 Veron (2000) Madrepora aspera Dana, 1846; Acropora cribripora (Dana, 1846); Madrepora cribripora Dana, 1846; Acropora manni (Quelch, 1886); Madrepora manni ACROPORIDAE Acropora aspera (Dana, 1846) Veron (2000) Quelch, 1886; Acropora hebes (Dana, 1846); Madrepora hebes Dana, 1846; Acropora yaeyamaensis Eguchi & Shirai, 1977 ACROPORIDAE Acropora austera (Dana, 1846) Veron (2000) Madrepora austera Dana, 1846 ACROPORIDAE Acropora awi Wallace & Wolstenholme, 1998 Veron (2000) ACROPORIDAE Acropora azurea Veron & Wallace, 1984 Veron (2000) ACROPORIDAE Acropora batunai Wallace, 1997 Veron (2000) ACROPORIDAE Acropora bifurcata Nemenzo, 1971 Veron (2000) ACROPORIDAE Acropora branchi Riegl, 1995 Veron (2000) Madrepora brueggemanni Brook, 1891; Isopora ACROPORIDAE Acropora brueggemanni (Brook, 1891) Veron (2000) brueggemanni (Brook, 1891) ACROPORIDAE Acropora bushyensis Veron & Wallace, 1984 Veron (2000) Acropora fasciculare Latypov, 1992 ACROPORIDAE Acropora cardenae Wells, 1985 Veron (2000) CoP16 Doc. -
Scleractinian Reef Corals: Identification Notes
SCLERACTINIAN REEF CORALS: IDENTIFICATION NOTES By JACKIE WOLSTENHOLME James Cook University AUGUST 2004 DOI: 10.13140/RG.2.2.24656.51205 http://dx.doi.org/10.13140/RG.2.2.24656.51205 Scleractinian Reef Corals: Identification Notes by Jackie Wolstenholme is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. TABLE OF CONTENTS TABLE OF CONTENTS ........................................................................................................................................ i INTRODUCTION .................................................................................................................................................. 1 ABBREVIATIONS AND DEFINITIONS ............................................................................................................. 2 FAMILY ACROPORIDAE.................................................................................................................................... 3 Montipora ........................................................................................................................................................... 3 Massive/thick plates/encrusting & tuberculae/papillae ................................................................................... 3 Montipora monasteriata .............................................................................................................................. 3 Massive/thick plates/encrusting & papillae ................................................................................................... -
A Unique Coral Biomineralization Pattern Has Resisted 40 Million Years of Major Ocean Chemistry Change
www.nature.com/scientificreports OPEN A unique coral biomineralization pattern has resisted 40 million years of major ocean chemistry Received: 14 December 2015 Accepted: 17 May 2016 change Published: 15 June 2016 Jarosław Stolarski1, Francesca R. Bosellini2, Carden C. Wallace3, Anne M. Gothmann4, Maciej Mazur5, Isabelle Domart-Coulon6, Eldad Gutner-Hoch7, Rolf D. Neuser8, Oren Levy7, Aldo Shemesh9 & Anders Meibom10,11 Today coral reefs are threatened by changes to seawater conditions associated with rapid anthropogenic global climate change. Yet, since the Cenozoic, these organisms have experienced major fluctuations in atmospheric CO2 levels (from greenhouse conditions of high pCO2 in the Eocene to low pCO2 ice-house conditions in the Oligocene-Miocene) and a dramatically changing ocean Mg/Ca ratio. Here we show that the most diverse, widespread, and abundant reef-building coral genus Acropora (20 morphological groups and 150 living species) has not only survived these environmental changes, but has maintained its distinct skeletal biomineralization pattern for at least 40 My: Well-preserved fossil Acropora skeletons from the Eocene, Oligocene, and Miocene show ultra-structures indistinguishable from those of extant representatives of the genus and their aragonitic skeleton Mg/Ca ratios trace the inferred ocean Mg/Ca ratio precisely since the Eocene. Therefore, among marine biogenic carbonate fossils, well-preserved acroporid skeletons represent material with very high potential for reconstruction of ancient ocean chemistry. Genomic sequencing has transformed our understanding of the evolution of scleractinian corals. However, the molecular clades defined for scleractinians are difficult to reconcile with traditional taxonomic classification based on overall skeletal morphology1–3. Instead, they have been shown to be broadly consistent with recently defined micro-morphological and ultrastructural skeletal criteria4–7. -
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. -
Scleractinia Fauna of Taiwan I
Scleractinia Fauna of Taiwan I. The Complex Group 台灣石珊瑚誌 I. 複雜類群 Chang-feng Dai and Sharon Horng Institute of Oceanography, National Taiwan University Published by National Taiwan University, No.1, Sec. 4, Roosevelt Rd., Taipei, Taiwan Table of Contents Scleractinia Fauna of Taiwan ................................................................................................1 General Introduction ........................................................................................................1 Historical Review .............................................................................................................1 Basics for Coral Taxonomy ..............................................................................................4 Taxonomic Framework and Phylogeny ........................................................................... 9 Family Acroporidae ............................................................................................................ 15 Montipora ...................................................................................................................... 17 Acropora ........................................................................................................................ 47 Anacropora .................................................................................................................... 95 Isopora ...........................................................................................................................96 Astreopora ......................................................................................................................99 -
Examining the Effect of Heat Stress on Montastraea Cavernosa
water Article Examining the Effect of Heat Stress on Montastraea cavernosa (Linnaeus 1767) from a Mesophotic Coral Ecosystem (MCE) John E. Skutnik 1, Sango Otieno 2 , Sok Kean Khoo 3 and Kevin B. Strychar 1,* 1 Annis Water Resources Institute, Grand Valley State University, Muskegon, MI 49441, USA; [email protected] 2 Department of Statistics, Grand Valley State University, Allendale, MI 49401, USA; [email protected] 3 Department Cell and Molecular Biology, Grand Valley State University, Allendale, MI 49401, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-616-331-8796 Received: 13 March 2020; Accepted: 29 April 2020; Published: 5 May 2020 Abstract: Coral reefs are under increasing pressure from global warming. Little knowledge, however, exists regarding heat induced stress on deeper mesophotic coral ecosystems (MCEs). Here, we examined the effect of acute (72 h) and chronic (480 h) heat stress on the host coral Montastraea cavernosa (Linnaeus 1767) collected from an upper MCE (~30 m) in Florida, USA. We examined six immune/stress-related genes: ribosomal protein L9 (RpL9), ribosomal protein S7 (RpS7), B-cell lymphoma 2 apoptosis regulator (BCL-2), heat shock protein 90 (HSP90), catalase, and cathepsin L1, as a proxy for coral response to heat stress. Quantitative real-time polymerase chain reaction (qRT-PCR) was performed to evaluate the gene expression. Overall, both acute and chronic heat stress treatments elicited a response in gene expression relative to control samples. Acute heat exposure resulted in up-regulation of catalase, BCL-2, and HSP90 at all time points from hour 24 to 48, suggesting the activation of an oxidative protective enzyme, molecular chaperone, and anti-apoptotic protein. -
Iranian Coral Reefs Status with Particular Reference to Kish Island, Persian Gulf
International Coral Reef Initiative Indian Ocean Regional Workshop, Muzambique, Nov. 26-28, 2001 IRANIAN CORAL REEFS STATUS WITH PARTICULAR REFERENCE TO KISH ISLAND, PERSIAN GULF 1 2 SEYED MOHAMMAD REZA FATEMI , MOHAMMAD REZA SHOKRI 1Dept. of Fisheries and Marine Biology, Science and Research Unit, Islamic Azad University, Hesarak, PO BOX: 14155-5655, Tehran, IRAN. Email: <[email protected]> 2Iranian National Center for Oceanography, #51, Bozorgmehr Ave., I4168, PO BOX: 14155- 4781, Tehran, IRAN. Email: <[email protected]> Abstract In this paper, the coral status of Iranian waters in the Persian Gulf are reviewed and discussed based on the obtained results and information after three years of field surveys in Nay Band Bay, Kish and Farur islands. Altogether, 27 species of corals were identified from the studied areas, belonging to 9 families and 20 genera. Faviidae with 6 genera and 8 species is the most diverse of all families. On the other hand, Poritidae with 2 genera and 4 species is the most abundant corals in all areas. In the last 10 years, Acropora has declined from being the most abundant genus in shallow waters of fringing islands, to almost absennt, due to environmental stresses and human impacts. Anacropora forbesi is reported for the first time from the area. Regarding the coral health, the live coral coverage ranges from 9 to 30%, with minimum coverage in Kish Island and maximum in Nay Band Bay. During this study, no new bleached coral was observed at the surveyed areas, though in the past few years, considerable bleaching events have occurred throughout the area. -
TUVALU MARINE LIFE PROJECT Phase 1: Literature Review
TUVALU MARINE LIFE PROJECT Phase 1: Literature review Project funded by: Tuvalu Marine Biodiversity – Literature Review Table of content TABLE OF CONTENT 1. CONTEXT AND OBJECTIVES 4 1.1. Context of the survey 4 1.1.1. Introduction 4 1.1.2. Tuvalu’s national adaptation programme of action (NAPA) 4 1.1.3. Tuvalu national biodiversity strategies and action plan (NBSAP) 5 1.2. Objectives 6 1.2.1. General objectives 6 1.2.2. Specific objectives 7 2. METHODOLOGY 8 2.1. Gathering of existing data 8 2.1.1. Contacts 8 2.1.2. Data gathering 8 2.1.3. Documents referencing 16 2.2. Data analysis 16 2.2.1. Data verification and classification 16 2.2.2. Identification of gaps 17 2.3. Planning for Phase 2 18 2.3.1. Decision on which survey to conduct to fill gaps in the knowledge 18 2.3.2. Work plan on methodologies for the collection of missing data and associated costs 18 3. RESULTS 20 3.1. Existing information on Tuvalu marine biodiversity 20 3.1.1. Reports and documents 20 3.1.2. Data on marine species 24 3.2. Knowledge gaps 41 4. WORK PLAN FOR THE COLLECTION OF FIELD DATA 44 4.1. Meetings in Tuvalu 44 4.2. Recommendations on field surveys to be conducted 46 4.3. Proposed methodologies 48 4.3.1. Option 1: fish species richness assessment 48 4.3.2. Option 2: valuable fish stock assessment 49 4.3.3. Option 3: fish species richness and valuable fish stock assessment 52 4.3.4. -
Regional Conservation Status of Scleractinian Coral Biodiversity in the Republic of the Marshall Islands
Diversity 2013, 5, 522-540; doi:10.3390/d5030522 OPEN ACCESS diversity ISSN 1424-2818 www.mdpi.com/journal/diversity Article Regional Conservation Status of Scleractinian Coral Biodiversity in the Republic of the Marshall Islands Zoe Richards 1,* and Maria Beger 2 1 Western Australian Museum, 49 Kew Street, Welshpool, WA 6105, Australia 2 ARC Centre of Excellence for Environmental Decisions, School of Biological Sciences, University of Queensland, Brisbane, QLD 4072, Australia; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +61-8-9212-3872; Fax: +61-8-9212-3885. Received: 5 April 2013; in revised form: 1 July 2013 / Accepted: 3 July 2013 / Published: 18 July 2013 Abstract: Preventing the loss of biodiversity is a major challenge in mega-diverse ecosystems such as coral reefs where there is a critical shortage of baseline demographic data. Threatened species assessments play a valuable role in guiding conservation action to manage and mitigate biodiversity loss, but they must be undertaken with precise information at an appropriate spatial scale to provide accurate classifications. Here we explore the regional conservation status of scleractinian corals on isolated Pacific Ocean atolls in the Republic of the Marshall Islands. We compile an integrated regional species list based upon new and historical records, and compare how well the regional threat classifications reflect species level priorities at a global scale. A similar proportion of the 240 species of hard coral recorded in the current survey are classified as Vulnerable at the regional scale as the global scale using the International Union for the Conservation of Nature (IUCN) Red List criteria (23% and 20% respectively), however there are distinct differences in the composition of species. -
A Unique Coral Biomineralization Pattern Has Resisted 40 Million Years of Major Ocean Chemistry Change
www.nature.com/scientificreports OPEN A unique coral biomineralization pattern has resisted 40 million years of major ocean chemistry Received: 14 December 2015 Accepted: 17 May 2016 change Published: 15 June 2016 Jarosław Stolarski1, Francesca R. Bosellini2, Carden C. Wallace3, Anne M. Gothmann4, Maciej Mazur5, Isabelle Domart-Coulon6, Eldad Gutner-Hoch7, Rolf D. Neuser8, Oren Levy7, Aldo Shemesh9 & Anders Meibom10,11 Today coral reefs are threatened by changes to seawater conditions associated with rapid anthropogenic global climate change. Yet, since the Cenozoic, these organisms have experienced major fluctuations in atmospheric CO2 levels (from greenhouse conditions of high pCO2 in the Eocene to low pCO2 ice-house conditions in the Oligocene-Miocene) and a dramatically changing ocean Mg/Ca ratio. Here we show that the most diverse, widespread, and abundant reef-building coral genus Acropora (20 morphological groups and 150 living species) has not only survived these environmental changes, but has maintained its distinct skeletal biomineralization pattern for at least 40 My: Well-preserved fossil Acropora skeletons from the Eocene, Oligocene, and Miocene show ultra-structures indistinguishable from those of extant representatives of the genus and their aragonitic skeleton Mg/Ca ratios trace the inferred ocean Mg/Ca ratio precisely since the Eocene. Therefore, among marine biogenic carbonate fossils, well-preserved acroporid skeletons represent material with very high potential for reconstruction of ancient ocean chemistry. Genomic sequencing has transformed our understanding of the evolution of scleractinian corals. However, the molecular clades defined for scleractinians are difficult to reconcile with traditional taxonomic classification based on overall skeletal morphology1–3. Instead, they have been shown to be broadly consistent with recently defined micro-morphological and ultrastructural skeletal criteria4–7. -
Coral Reefs of Japan
Appendix 4 A list of Hermatypic corals in Japan ① This list is based on a table in 'Hermatypic corals of Japan' (Nishihira and Veron 1995). ● Species reported by Veron (1993) ○ Species reported by the followings articles; Tribble and Randall (1986)(Miyakejima), Tachikawa (unpublished), and Tachikawa (1991)(Ogasawara) referenced by Veron (1992). Dai(1991) (Taiwan), Matsumoto (unpublished)(Miyakojima) and other observations. ② Japan Wildlife Research Center added the latest information from the distribution map of 'Corals of the World' (Veron 2000). ◎: Species added from Veron (2000) ×: Species deleted by Veron (2000) The coral distribution of Miyake Island, Boso Peninsula and Izu Peninsula are not clearly distinguished from other areas on the map in Veron (2000). Therefore coral species for these areas are marked (△), and not counted in the total number of species. In Veron(2000), the scientific names of some species are changed. This list includes both species name in Veron (2000) and Nishihira and Veron (1995) (* is marked in front of scientific name). ③ For reference, the species distributed in the Philippines and Taiwan are shown on the left column on the list. This list dose not include all the species in those two countries. Region Species name Remarks ii Peninsula) Philippines Taiwan Yaeyama Archipelago Miyako Archipelago Islands Okinawa Amami Archipelago Tanegashima (Osumi Islands) Amakusa (Kyushu) Tosashimizu (Shikoku) Shirahama (Kii Peninsula) Kushimoto (K Izu Peninsula Tateyama (Boso Peninsula) Miyake Island (Izu Islands) Islands