Reef-Building Corals (Cnidaria: Scleractinia) from the Watamu Marine National Reserve, Kenya; an Annotated Species List
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Reproductive Strategies of the Coral Turbinaria Reniformis in The
www.nature.com/scientificreports OPEN Reproductive strategies of the coral Turbinaria reniformis in the northern Gulf of Aqaba (Red Sea) Received: 10 October 2016 Hanna Rapuano1, Itzchak Brickner1, Tom Shlesinger1, Efrat Meroz-Fine2, Raz Tamir1,2 & Accepted: 13 January 2017 Yossi Loya1 Published: 14 February 2017 Here we describe for the first time the reproductive biology of the scleractinian coralTurbinaria reniformis studied during three years at the coral reefs of Eilat and Aqaba. We also investigated the possibility of sex change in individually tagged colonies followed over a period of 12 years. T. reniformis was found to be a stable gonochorist (no detected sex change) that reproduces by broadcast spawning 5–6 nights after the full moon of June and July. Spawning was highly synchronized between individuals in the field and in the lab. Reproduction ofT. reniformis is temporally isolated from the times at which most other corals reproduce in Eilat. Its relatively long reproductive cycle compared to other hermaphroditic corals may be due to the high reproductive effort associated with the production of eggs by gonochoristic females. Sex ratio in both the Aqaba and Eilat coral populations deviated significantly from a 1:1 ratio. The larger number of males than of females may provide a compensation for sperm limitation due to its dilution in the water column. We posit that such sex allocation would facilitate adaptation within gonochoristic species by increasing fertilization success in low density populations, constituting a phenomenon possibly regulated by chemical communication. Research on scleractinian coral reproduction is a prerequisite for the study of other life-history strategies, the ecol- ogy and persistence of populations and communities, and for the management and preservation of the reef1–3. -
(Symbiodinium) in Scleractinian Corals from Tropical Reefs in Southern Hainan
Journal of Systematics and Evolution 49 (6): 598–605 (2011) doi: 10.1111/j.1759-6831.2011.00161.x Research Article Low genetic diversity of symbiotic dinoflagellates (Symbiodinium) in scleractinian corals from tropical reefs in southern Hainan Island, China 1,2Guo-Wei ZHOU 1,2Hui HUANG∗ 1(Key Laboratory of Marine Bio-resources Sustainable Utilization, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China) 2(Tropical Marine Biological Research Station in Hainan, Chinese Academy of Sciences, Sanya 572000, China) Abstract Endosymbiotic dinoflagellates in the genus Symbiodinium are among the most abundant and important group of photosynthetic protists found in coral reef ecosystems. In order to further characterize this diversity and compare with other regions of the Pacific, samples from 44 species of scleractinian corals representing 20 genera and 9 families, were collected from tropical reefs in southern Hainan Island, China. Denaturing gradient gel electrophoresis fingerprinting of the ribosomal internal transcribed spacer 2 identified 11 genetically distinct Symbiodinium types that have been reported previously. The majority of reef-building coral species (88.6%) harbored only one subcladal type of symbiont, dominated by host-generalist C1 and C3, and was influenced little by the host’s apparent mode of symbiont acquisition. Some species harbored more than one clade of Symbiodinium (clades C, D) concurrently. Although geographically isolated from the rest of the Pacific, the symbiont diversity in southern Hainan Island was relatively low and similar to both the Great Barrier Reef and Hawaii symbiont assemblages (dominated by clade C Symbiodinium). These results indicate that a specialist symbiont is not a prerequisite for existence in remote and isolated areas, but additional work in other geographic regions is necessary to test this idea. -
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. -
SEDIMENTARY FRAMEWORK of Lmainland FRINGING REEF DEVELOPMENT, CAPE TRIBULATION AREA
GREAT BARRIER REEF MARINE PARK AUTHORITY TECHNICAL MEMORANDUM GBRMPA-TM-14 SEDIMENTARY FRAMEWORK OF lMAINLAND FRINGING REEF DEVELOPMENT, CAPE TRIBULATION AREA D.P. JOHNSON and RM.CARTER Department of Geology James Cook University of North Queensland Townsville, Q 4811, Australia DATE November, 1987 SUMMARY Mainland fringing reefs with a diverse coral fauna have developed in the Cape Tribulation area primarily upon coastal sedi- ment bodies such as beach shoals and creek mouth bars. Growth on steep rocky headlands is minor. The reefs have exten- sive sandy beaches to landward, and an irregular outer margin. Typically there is a raised platform of dead nef along the outer edge of the reef, and dead coral columns lie buried under the reef flat. Live coral growth is restricted to the outer reef slope. Seaward of the reefs is a narrow wedge of muddy, terrigenous sediment, which thins offshore. Beach, reef and inner shelf sediments all contain 50% terrigenous material, indicating the reefs have always grown under conditions of heavy terrigenous influx. The relatively shallow lower limit of coral growth (ca 6m below ADD) is typical of reef growth in turbid waters, where decreased light levels inhibit coral growth. Radiocarbon dating of material from surveyed sites confirms the age of the fossil coral columns as 33304110 ybp, indicating that they grew during the late postglacial sea-level high (ca 5500-6500 ybp). The former thriving reef-flat was killed by a post-5500 ybp sea-level fall of ca 1 m. Although this study has not assessed the community structure of the fringing reefs, nor whether changes are presently occur- ring, it is clear the corals present today on the fore-reef slope have always lived under heavy terrigenous influence, and that the fossil reef-flat can be explained as due to the mid-Holocene fall in sea-level. -
Ammonium Contribution from Boring Bivalves to Their Coral Host -A Mutualistic Symbiosis?
MARINE ECOLOGY PROGRESS SERIES Vol. 169: 295-301, 1998 Published August 6 Mar Ecol Prog Ser p Ammonium contribution from boring bivalves to their coral host -a mutualistic symbiosis? Ofer ~okady'.',Yossi ~oya~,Boaz ~azar~ 'Institute for Nature Conservation Research and 'Department of Zoology, George S. Wise Faculty of Life Sciences, and the Porter Super- Center for Ecological and Environmental Studies, Tel-Aviv University, Tel-Aviv 69978, Israel Institute of Earth Sciences and Moshe Shilo Minerva Center for Marine Biogeochemistry, The Hebrew University of Jerusalem. Jerusalem 91904, Israel ABSTRACT: The mytilid bivalve Lithophaga simplex is found within its tissue, offers an example for such a nitrogen- to inhabit the scleractinian coral Astreopora myriophthalma recycling system (Hawkins & Klumpp 1995). in high densities. This boring bivalve, living inside the CaC03 Aspects of ammonium uptake have been studied in skeleton of the coral, produces considerable amounts of ammonium as a nitrogenous waste product. Ammonium pro- many algae-invertebrate associations (e.g. Wilkerson duction rate by the bivalves and consumption rate by the & Trench 1986, Fitt et al. 1993). The association be- coral (via the symbiotic algae) were measured in laboratory tween hermatypic corals (Order Scleractinia) and the expenments. The population density of L. simplex bivalves dinoflagellate endosymbiont Symbiodinium sp. is a In A. myri~phth~lrnacorals was surveyed in the Nature Reserve Reef, Eilat, Red Sea, Israel. Ammonium production very common symbiotic relationship in tropical and rate by the bivalves, inhabiting the coral at a density of 0.22 +_ subtropical marine environments (Falkowski et al. 0.11 bivalves cm-', is calculated to be 8.2 i 3.8 and 3.5 1984). -
Species Diversity of Mushroom Corals (Family Fungiidae) in the Inner Gulf of Thailand
The Natural History Journal of Chulalongkorn University 2(2): 47-49, August 2002 ©2002 by Chulalongkorn University Species Diversity of Mushroom Corals (Family Fungiidae) in the Inner Gulf of Thailand LALITA PUTCHIM, SUCHANA CHAVANICH * AND VORANOP VIYAKARN Department of Marine Science, Faculty of Science, Chulalongkorn University, Bangkok 10330, THAILAND Mushroom coral (Family Fungiidae) is one islands (Fig. 1, Table 1). These species included of the most conspicuous groups in the tropical Ctenactis crassa (Dana, 1846), C. echinata Indo-Pacific reefs. These corals usually aggre- (Pallas, 1766), Fungia fungites (Linnaeus, gate in large clumps that are able to create the 1758), Lithophyllon undulatum Rehberg, 1892, reef formation (Pichon, 1974; Littler et al., Podabacia crustacea (Pallas, 1766), and Poly- 1997). In the tropical Indo-Pacific region, 41 phyllia talpina (Lamarck, 1801) (Fig. 1). Each species of fungiid corals have been found (Hoek- study site had four species of fungiids, but only sema, 1989). However, their biogeography is two species overlapped between the two sites. yet still unclear. In the Gulf of Thailand, little F. fungites, C. echinata, L. undulatum, and P. is known about the species diversity of fungiids crustacea were found at Ko Kham while F. and their distribution. Seven species were fungites, C. crassa, C. echinata, and P. talpina recorded by field survey at the Sichang Islands, were found at Ko Khram. Chon Buri Province (Sakai et al., 1986; Sara- From observations at Ko Khram and Ko sas, 1994), and 14 species were found in the Kham, it is interesting to note that more than coral collections at the institutes and museums 50% of live corals found in the study areas around the country (Jiravat, 1985). -
Reef Structures Subject Matter: Recall the Different Types of Reef Structure (E.G
THE REEF AND BEYOND - CORAL REEF DISTRIBUTION Reef Structures Subject matter: Recall the different types of reef structure (e.g. fringing, platform, ribbon, barrier, atolls, coral cays). Recommended reading: Coral Reefs and Climate Change - Patterns of distribution (p.84-85) Zones across the reef (p.92-94) FRINGING REEF Fringing reefs are reefs that grow directly from a shore, with no “true” lagoon (i.e., deep water channel) between the reef and the nearby land. Without an intervening lagoon to effectively buffer freshwater runoff, pollution, and sedimentation, fringing reefs tend to particularly sensitive to these forms of human impact. Fringing reef Tane Sinclair Taylor Tane Tane Sinclair Taylor Tane Planet Dove - Allen Coral Atlas Allen Coral Planet Dove - Coral coast, Fiji Fringing reef in Indonesia. PLATFORM REEFS AND CORAL CAYS Platform reefs begin to form on underwater mountains or other rock-hard outcrops between the shore and a barrier reef. Coral cays begin to form when broken coral and sand wash onto these flats; cays can also form on shallow reefs around atolls. Coral cays are small islands, with Platform reef and Coral cay typical length scales between 100 - 1000 m, that form on platform reefs, Dave Logan Heron Island Lady Elliot Island Marine Science Senior Syllabus 8 THE REEF AND BEYOND - CORAL REEF DISTRIBUTION Reef Structures BARRIER REEFS BARRIER REEFS are coral reefs roughly parallel to a RIBBON REEFS are a type of barrier reef and are unique shore and separated from it by a lagoon or other body of to Australia. The name relates to the elongated Reef water.The coral reef structure buffers shorelines against bodies starting to the north of Cairns, and finishing to the waves, storms, and floods, helping to prevent loss of life, east of Lizard Island. -
Growth and Population Dynamic Model of the Reef Coral Fungia Granulosa Klunzinger, 1879 at Eilat, Northern Red Sea
Journal of Experimental Marine Biology and Ecology View metadata, citation and similar papers at core.ac.uk L brought to you by CORE 249 (2000) 199±218 www.elsevier.nl/locate/jembe provided by Almae Matris Studiorum Campus Growth and population dynamic model of the reef coral Fungia granulosa Klunzinger, 1879 at Eilat, northern Red Sea Nanette E. Chadwick-Furmana,b,* , Stefano Goffredo c , Yossi Loya d aInteruniversity Institute for Marine Science, P.O. Box 469, Eilat, Israel bFaculty of Life Sciences, Bar Ilan University, Ramat Gan, Israel cDepartment of Evolutionary and Experimental Biology, University of Bologna, via Selmi 3, I-40126 Bologna, Italy dDepartment of Zoology, The George S. Wise Faculty of Life Sciences, and the Porter Super-Center for Ecological and Environmental Studies, Tel Aviv University, Tel Aviv, Israel Received 18 August 1999; received in revised form 10 February 2000; accepted 9 March 2000 Abstract The lack of population dynamic information for most species of stony corals is due in part to their complicated life histories that may include ®ssion, fusion and partial mortality of colonies, leading to an uncoupling of coral age and size. However, some reef-building corals may produce compact upright or free-living individuals in which the above processes rarely occur, or are clearly detectable. In some of these corals, individual age may be determined from size, and standard growth and population dynamic models may be applied to gain an accurate picture of their life history. We measured long-term growth rates (up to 2.5 years) of individuals of the free-living mushroom coral Fungia granulosa Klunzinger, 1879 at Eilat, northern Red Sea, and determined the size structure of a population on the shallow reef slope. -
Resurrecting a Subgenus to Genus: Molecular Phylogeny of Euphyllia and Fimbriaphyllia (Order Scleractinia; Family Euphylliidae; Clade V)
Resurrecting a subgenus to genus: molecular phylogeny of Euphyllia and Fimbriaphyllia (order Scleractinia; family Euphylliidae; clade V) Katrina S. Luzon1,2,3,*, Mei-Fang Lin4,5,6,*, Ma. Carmen A. Ablan Lagman1,7, Wilfredo Roehl Y. Licuanan1,2,3 and Chaolun Allen Chen4,8,9,* 1 Biology Department, De La Salle University, Manila, Philippines 2 Shields Ocean Research (SHORE) Center, De La Salle University, Manila, Philippines 3 The Marine Science Institute, University of the Philippines, Quezon City, Philippines 4 Biodiversity Research Center, Academia Sinica, Taipei, Taiwan 5 Department of Molecular and Cell Biology, James Cook University, Townsville, Australia 6 Evolutionary Neurobiology Unit, Okinawa Institute of Science and Technology Graduate University, Okinawa, Japan 7 Center for Natural Sciences and Environmental Research (CENSER), De La Salle University, Manila, Philippines 8 Taiwan International Graduate Program-Biodiversity, Academia Sinica, Taipei, Taiwan 9 Institute of Oceanography, National Taiwan University, Taipei, Taiwan * These authors contributed equally to this work. ABSTRACT Background. The corallum is crucial in building coral reefs and in diagnosing systematic relationships in the order Scleractinia. However, molecular phylogenetic analyses revealed a paraphyly in a majority of traditional families and genera among Scleractinia showing that other biological attributes of the coral, such as polyp morphology and reproductive traits, are underutilized. Among scleractinian genera, the Euphyllia, with nine nominal species in the Indo-Pacific region, is one of the groups Submitted 30 May 2017 that await phylogenetic resolution. Multiple genetic markers were used to construct Accepted 31 October 2017 Published 4 December 2017 the phylogeny of six Euphyllia species, namely E. ancora, E. divisa, E. -
Composition and Ecology of Deep-Water Coral Associations D
HELGOLK---~DER MEERESUNTERSUCHUNGEN Helgoltinder Meeresunters. 36, 183-204 (1983) Composition and ecology of deep-water coral associations D. H. H. Kfihlmann Museum ffir Naturkunde, Humboldt-Universit~t Berlin; Invalidenstr. 43, DDR- 1040 Berlin, German Democratic Republic ABSTRACT: Between 1966 and 1978 SCUBA investigations were carried out in French Polynesia, the Red Sea, and the Caribbean, at depths down to 70 m. Although there are fewer coral species in the Caribbean, the abundance of Scleractinia in deep-water associations below 20 m almost equals that in the Indian and Pacific Oceans. The assemblages of corals living there are described and defined as deep-water coral associations. They are characterized by large, flattened growth forms. Only 6 to 7 % of the species occur exclusively below 20 m. More than 90 % of the corals recorded in deep waters also live in shallow regions. Depth-related illumination is not responsible for depth differentiations of coral associations, but very likely, a complex of mechanical factors, such as hydrodynamic conditions, substrate conditions, sedimentation etc. However, light intensity deter- mines the general distribution of hermatypic Scleractinia in their bathymetric range as well as the platelike shape of coral colonies characteristic for deep water associations. Depending on mechani- cal factors, Leptoseris, Montipora, Porites and Pachyseris dominate as characteristic genera in the Central Pacific Ocean, Podabacia, Leptoseris, Pachyseris and Coscinarea in the Red Sea, Agaricia and Leptoseris in the tropical western Atlantic Ocean. INTRODUCTION Considerable attention has been paid to shallow-water coral associations since the first half of this century (Duerden, 1902; Mayer, 1918; Umbgrove, 1939). Detailed investigations at depths down to 20 m became possible only through the use of autono- mous diving apparatus. -
Notification 2013/035
CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA NOTIFICATION TO THE PARTIES No. 2013/035 Geneva, 16 August 2013 CONCERNING: Trade in stony corals List of coral taxa where identification to genus level is acceptable 1. At its 18th meeting (San José, April 2002), the Animals Committee adopted a list of coral genera that could be identified to the species level and of those that could be identified to the genus level only. These lists were accepted by the Conference of the Parties at its 12th meeting (Santiago, 2002) and disseminated by the Secretariat through Notification to the Parties No. 2003/020 of 4 April 2003. 2. At its 15th meeting (CoP15, Doha, 2010), the Conference of the Parties instructed the Secretariat to re- issue Notification to the Parties No. 2003/020 without the list of stony coral taxa identifiable to species level. The Secretariat therefore issued Notification to the Parties No. 2010/014 of 17 June 2010, providing the list of stony coral genera for which identification to genus level only is acceptable. In addition, at CoP15, the Conference instructed the Animals Committee to update this list. 3. At its 26th meeting (Geneva, March 2012), the Animals Committee adopted a revised list of stony coral genera for which identification to genus level only is acceptable for the purpose of implementing Resolutions Conf. 11.17 (Rev. CoP16) on National reports and Conf. 12.3 (Rev. CoP16) on Permits and certificates. The revised list was presented in Notification to the Parties No. 2012/047 of 19 July 2012.