Diversity, Distribution and Biological Activity of Soft Corals (Octocorallia, Alcyonacea) in Singapore
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Precious Corals (Coralliidae) from North-Western Atlantic Seamounts A
The University of Maine DigitalCommons@UMaine Marine Sciences Faculty Scholarship School of Marine Sciences 3-1-2011 Precious Corals (Coralliidae) from North-Western Atlantic Seamounts A. Simpson Les Watling University of Maine - Main, [email protected] Follow this and additional works at: https://digitalcommons.library.umaine.edu/sms_facpub Repository Citation Simpson, A. and Watling, Les, "Precious Corals (Coralliidae) from North-Western Atlantic Seamounts" (2011). Marine Sciences Faculty Scholarship. 97. https://digitalcommons.library.umaine.edu/sms_facpub/97 This Article is brought to you for free and open access by DigitalCommons@UMaine. It has been accepted for inclusion in Marine Sciences Faculty Scholarship by an authorized administrator of DigitalCommons@UMaine. For more information, please contact [email protected]. Journal of the Marine Biological Association of the United Kingdom, 2011, 91(2), 369–382. # Marine Biological Association of the United Kingdom, 2010 doi:10.1017/S002531541000086X Precious corals (Coralliidae) from north-western Atlantic Seamounts anne simpson1 and les watling1,2 1Darling Marine Center, University of Maine, Walpole, ME 04573, USA, 2Department of Zoology, University of Hawaii at Manoa, Honolulu, HI 96822, USA Two new species belonging to the precious coral genus Corallium were collected during a series of exploratory cruises to the New England and Corner Rise Seamounts in 2003–2005. One red species, Corallium bathyrubrum sp. nov., and one white species, C. bayeri sp. nov., are described. Corallium bathyrubrum is the first red Corallium to be reported from the western Atlantic. An additional species, C. niobe Bayer, 1964 originally described from the Straits of Florida, was also collected and its description augmented. -
Slow Population Turnover in the Soft Coral Genera Sinularia and Sarcophyton on Mid- and Outer-Shelf Reefs of the Great Barrier Reef
MARINE ECOLOGY PROGRESS SERIES Vol. 126: 145-152,1995 Published October 5 Mar Ecol Prog Ser l Slow population turnover in the soft coral genera Sinularia and Sarcophyton on mid- and outer-shelf reefs of the Great Barrier Reef Katharina E. Fabricius* Australian Institute of Marine Science, PMB 3, Townsville, Queensland 4810, Australia ABSTRACT: Aspects of the life history of the 2 common soft coral genera Sinularja and Sarcophyton were investigated on 360 individually tagged colonies over 3.5 yr. Measurements included rates of growth, colony fission, mortality, sublethal predation and algae infection, and were carried out at 18 sites on 6 mid- and outer-shelf reefs of the Australian Great Barrier Reef. In both Sinularia and Sarco- phyton, average radial growth was around 0.5 cm yr.', and relative growth rates were size-dependent. In Sinularia, populations changed very slowly over time. Their per capita mortality was low (0.014 yr.') and size-independent, and indicated longevity of the colonies. Colonies with extensions of up to 10 X 10 m potentially could be several hundreds of years old. Mortality was more than compensated for by asexual reproduction through colony fission (0.035 yr.'). In Sarcophyton, mortality was low in colonies larger than 5 cm disk diameter (0.064 yr-l), and significantly higher in newly recruited small colonies (0.88 yr-'). Photographic monitoring of about 500 additional colonies from 16 soft coral genera showed that rates of mortality and recruitment In the family Alcyoniidae differed fundamentally from those of the commonly more 'fugitive' families Xeniidae and Nephtheidae. Rates of recruitment by larval set- tlement were very low in a majority of the soft coral taxa. -
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. -
Microbiomes of Gall-Inducing Copepod Crustaceans from the Corals Stylophora Pistillata (Scleractinia) and Gorgonia Ventalina
www.nature.com/scientificreports OPEN Microbiomes of gall-inducing copepod crustaceans from the corals Stylophora pistillata Received: 26 February 2018 Accepted: 18 July 2018 (Scleractinia) and Gorgonia Published: xx xx xxxx ventalina (Alcyonacea) Pavel V. Shelyakin1,2, Sofya K. Garushyants1,3, Mikhail A. Nikitin4, Sofya V. Mudrova5, Michael Berumen 5, Arjen G. C. L. Speksnijder6, Bert W. Hoeksema6, Diego Fontaneto7, Mikhail S. Gelfand1,3,4,8 & Viatcheslav N. Ivanenko 6,9 Corals harbor complex and diverse microbial communities that strongly impact host ftness and resistance to diseases, but these microbes themselves can be infuenced by stresses, like those caused by the presence of macroscopic symbionts. In addition to directly infuencing the host, symbionts may transmit pathogenic microbial communities. We analyzed two coral gall-forming copepod systems by using 16S rRNA gene metagenomic sequencing: (1) the sea fan Gorgonia ventalina with copepods of the genus Sphaerippe from the Caribbean and (2) the scleractinian coral Stylophora pistillata with copepods of the genus Spaniomolgus from the Saudi Arabian part of the Red Sea. We show that bacterial communities in these two systems were substantially diferent with Actinobacteria, Alphaproteobacteria, and Betaproteobacteria more prevalent in samples from Gorgonia ventalina, and Gammaproteobacteria in Stylophora pistillata. In Stylophora pistillata, normal coral microbiomes were enriched with the common coral symbiont Endozoicomonas and some unclassifed bacteria, while copepod and gall-tissue microbiomes were highly enriched with the family ME2 (Oceanospirillales) or Rhodobacteraceae. In Gorgonia ventalina, no bacterial group had signifcantly diferent prevalence in the normal coral tissues, copepods, and injured tissues. The total microbiome composition of polyps injured by copepods was diferent. -
Long-Term Recruitment of Soft-Corals (Octocorallia: Alcyonacea) on Artificial Substrata at Eilat (Red Sea)
MARINE ECOLOGY - PROGRESS SERIES Vol. 38: 161-167, 1987 Published June 18 Mar. Ecol. Prog. Ser. Long-term recruitment of soft-corals (Octocorallia: Alcyonacea) on artificial substrata at Eilat (Red Sea) Y.Benayahu & Y.Loya Department of Zoology. The George S. Wise Center for Life Sciences, Tel Aviv University, Tel Aviv 69978. Israel ABSTRACT: Recruitment of soft corals (Octocorallia: Alcyonacea) on concrete plates was studied in the reefs of the Nature Reserve of Eilat at depths of 17 to 29 m over 12 yr. Xenia macrospiculata was the pioneering species, appealing on the vast majority of the plates before any other spat. This species remained the most conspicuous inhabitant of the substrata throughout the whole study. Approximately 10 % of the plates were very extensively colonized by X. rnacrospiculata, resembling the percentage of living coverage by the species in the surrounding reef, thus suggesting that during the study X. rnacrospiculata populations reached their maximal potential to capture the newly available substrata. The successive appearance of an additional 11 soft coral species was recorded. The species composition of the recruits and their abundance corresponded with the soft coral community in the natural reef, indicahng that the estabhshed spat were progeny of the local populations. Soft coral recruits utilized the edges and lower surfaces of the plates most successfully, rather than the exposed upper surfaces. Such preferential settling of alcyonaceans allows the spat to escape from unfavourable conditions and maintains their high survival in the established community. INTRODUCTION determine the role played by alcyonaceans in the course of reef colonization and in the reef's space Studies on processes and dynamics of reef benthic allocation. -
Coral Feeding on Microalgae Assessed with Molecular Trophic Markers
Molecular Ecology (2013) doi: 10.1111/mec.12486 Coral feeding on microalgae assessed with molecular trophic markers MIGUEL C. LEAL,*† CHRISTINE FERRIER-PAGES,‡ RICARDO CALADO,* MEGAN E. THOMPSON,† MARC E. FRISCHER† and JENS C. NEJSTGAARD† *Departamento de Biologia & CESAM, Universidade de Aveiro, Campus Universitario de Santiago, 3810-193 Aveiro, Portugal, †Skidaway Institute of Oceanography, 10 Ocean Science Circle, 31411 Savannah, GA, USA, ‡Centre Scientifique de Monaco, Avenue St-Martin, 98000 Monaco, Monaco Abstract Herbivory in corals, especially for symbiotic species, remains controversial. To investi- gate the capacity of scleractinian and soft corals to capture microalgae, we conducted controlled laboratory experiments offering five algal species: the cryptophyte Rhodo- monas marina, the haptophytes Isochrysis galbana and Phaeocystis globosa, and the diatoms Conticribra weissflogii and Thalassiosira pseudonana. Coral species included the symbiotic soft corals Heteroxenia fuscescens and Sinularia flexibilis, the asymbiotic scleractinian coral Tubastrea coccinea, and the symbiotic scleractinian corals Stylophora pistillata, Pavona cactus and Oculina arbuscula. Herbivory was assessed by end-point PCR amplification of algae-specific 18S rRNA gene fragments purified from coral tissue genomic DNA extracts. The ability to capture microalgae varied with coral and algal species and could not be explained by prey size or taxonomy. Herbivory was not detected in S. flexibilis and S. pistillata. P. globosa was the only algal prey that was never captured by any coral. Although predation defence mechanisms have been shown for Phaeocystis spp. against many potential predators, this study is the first to suggest this for corals. This study provides new insights into herbivory in symbiotic corals and suggests that corals may be selective herbivorous feeders. -
Chapter Two Marine Organisms
THE SINGAPORE BLUE PLAN 2018 EDITORS ZEEHAN JAAFAR DANWEI HUANG JANI THUAIBAH ISA TANZIL YAN XIANG OW NICHOLAS YAP PUBLISHED BY THE SINGAPORE INSTITUTE OF BIOLOGY OCTOBER 2018 THE SINGAPORE BLUE PLAN 2018 PUBLISHER THE SINGAPORE INSTITUTE OF BIOLOGY C/O NSSE NATIONAL INSTITUTE OF EDUCATION 1 NANYANG WALK SINGAPORE 637616 CONTACT: [email protected] ISBN: 978-981-11-9018-6 COPYRIGHT © TEXT THE SINGAPORE INSTITUTE OF BIOLOGY COPYRIGHT © PHOTOGRAPHS AND FIGURES BY ORINGAL CONTRIBUTORS AS CREDITED DATE OF PUBLICATION: OCTOBER 2018 EDITED BY: Z. JAAFAR, D. HUANG, J.T.I. TANZIL, Y.X. OW, AND N. YAP COVER DESIGN BY: ABIGAYLE NG THE SINGAPORE BLUE PLAN 2018 ACKNOWLEDGEMENTS The editorial team owes a deep gratitude to all contributors of The Singapore Blue Plan 2018 who have tirelessly volunteered their expertise and effort into this document. We are fortunate to receive the guidance and mentorship of Professor Leo Tan, Professor Chou Loke Ming, Professor Peter Ng, and Mr Francis Lim throughout the planning and preparation stages of The Blue Plan 2018. We are indebted to Dr. Serena Teo, Ms Ria Tan and Dr Neo Mei Lin who have made edits that improved the earlier drafts of this document. We are grateful to contributors of photographs: Heng Pei Yan, the Comprehensive Marine Biodiversity Survey photography team, Ria Tan, Sudhanshi Jain, Randolph Quek, Theresa Su, Oh Ren Min, Neo Mei Lin, Abraham Matthew, Rene Ong, van Heurn FC, Lim Swee Cheng, Tran Anh Duc, and Zarina Zainul. We thank The Singapore Institute of Biology for publishing and printing the The Singapore Blue Plan 2018. -
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. -
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. -
Rearing Cuttings of the Soft Coral Sarcophyton Glaucum (Octocorallia, Alcyonacea): Towards Mass Production in a Closed Seawater System
Aquaculture Research, 2010, 41,1748^1758 doi:10.1111/j.1365-2109.2009.02475.x Rearing cuttings of the soft coral Sarcophyton glaucum (Octocorallia, Alcyonacea): towards mass production in a closed seawater system Ido Sella & Yehuda Benayahu Department of Zoology,George S.Wise Faculty of Life Sciences,Tel-Aviv University,Tel-Aviv, Israel Correspondence: I Sella, Department of Zoology,George S.Wise Faculty of Life Sciences,Tel-Aviv University,Tel-Aviv 69978, Israel. E-mail: [email protected] Abstract for diverse natural products with pharmaceutical or cosmetic value (e.g., Blunt, Copp, Munro, Northcote & The octcoral Sarcophyton glaucum has a wide Indo- Prinsep 2005; Slattery, Gochfeld & Kamel 2005; Sip- Paci¢c distribution and is known for its diverse con- kema, Osinga, Schatton, Mendola,Tramper & Wij¡els tent of natural products.The aim of the current study 2005), as well as for the reef-aquarium trade (Wab- was to establish a protocol for rearing miniature cut- nitz,Taylor, Grenn & Razak 2003). The increased de- tings of S. glaucum in a closed seawater system. In or- mand for these organisms has led to their massive der to determine the optimal conditions for rearing, harvesting (Castanaro & Lasker 2003) and has raised the survival, average dry weight, percentage of or- the need for e⁄cient farming methodologies (Ellis & ganic weight and development of the cuttings were Ellis 2002; Mendola 2003). monitored under di¡erent temperature, light, salinity Coral propagation has been commonly used for the and feeding regimes. At 26 1C, the highest dry weight production of daughter colonies, rather than harvest- was obtained, and at 20 1C, the highest percentage of ing naturally grown ones (e.g., Soong & Chen 2003; organic weight. -
Do Singapore's Seawalls Host Non-Native Marine Molluscs?
Aquatic Invasions (2018) Volume 13, Issue 3: 365–378 DOI: https://doi.org/10.3391/ai.2018.13.3.05 Open Access © 2018 The Author(s). Journal compilation © 2018 REABIC Research Article Do Singapore’s seawalls host non-native marine molluscs? Wen Ting Tan1, Lynette H.L. Loke1, Darren C.J. Yeo2, Siong Kiat Tan3 and Peter A. Todd1,* 1Experimental Marine Ecology Laboratory, Department of Biological Sciences, National University of Singapore, 16 Science Drive 4, Block S3, #02-05, Singapore 117543 2Freshwater & Invasion Biology Laboratory, Department of Biological Sciences, National University of Singapore, 16 Science Drive 4, Block S3, #02-05, Singapore 117543 3Lee Kong Chian Natural History Museum, Faculty of Science, National University of Singapore, 2 Conservatory Drive, Singapore 117377 *Corresponding author E-mail: [email protected] Received: 9 March 2018 / Accepted: 8 August 2018 / Published online: 17 September 2018 Handling editor: Cynthia McKenzie Abstract Marine urbanization and the construction of artificial coastal structures such as seawalls have been implicated in the spread of non-native marine species for a variety of reasons, the most common being that seawalls provide unoccupied niches for alien colonisation. If urbanisation is accompanied by a concomitant increase in shipping then this may also be a factor, i.e. increased propagule pressure of non-native species due to translocation beyond their native range via the hulls of ships and/or in ballast water. Singapore is potentially highly vulnerable to invasion by non-native marine species as its coastline comprises over 60% seawall and it is one of the world’s busiest ports. The aim of this study is to investigate the native, non-native, and cryptogenic molluscs found on Singapore’s seawalls. -
New Cytotoxic Cembranoid from Indonesian Soft Coral Sarcophyton Sp
Pharmacogn. Res. ORIGINAL ARTICLE A multifaceted peer reviewed journal in the field of Pharmacognosy and Natural Products www.phcogres.com | www.phcog.net New Cytotoxic Cembranoid from Indonesian Soft Coral Sarcophyton sp. Hedi Indra Januar1,2, Neviaty Putri Zamani2, Dedi Soedharma2, Ekowati Chasanah1 1Department of Biotechnology, Indonesian Research and Development Center for Marine and Fisheries Products Processing and Biotechnology, Jakarta, 2Department of Marine Science, Faculty of Fisheries and Marine Science, Bogor Agricultural University, Bogor, Indonesia ABSTRACT Context: Sarcophyton is a soft coral species that contains various secondary metabolites with cytotoxic activity. The production of cytotoxic compounds in soft corals is suggested as their allelochemical to win space competition. Therefore, if a particular soft coral species dominates a reef area, it may suggest to contain interesting bioactive compounds. Aims: This research aimed to characterize the cytotoxic compounds in dominant soft coral species (Sarcophyton sp.) on the reef at the Western side of Mahengetang Island, Indonesia. Subjects and Methods: Isolation of cytotoxic compounds through ethanol extracts had been done with preparative high-performance liquid chromatography and bioassay-guided fractionation by MCF-7 (breast) cancer cell lines. The structures of each cytotoxic compounds were elucidated on the basis of mass and nuclear magnetic resonance spectroscopic studies. Results: Elucidation through all compounds found a new cembranoid, namely, 2-hydroxy-crassocolide E (1), Abbreviations Used: SCUBA: Self-contained underwater breathing apparatus; alongside with 5 known cembranoids; sarcophytoxide (2), sarcrassin E HPLC: High performance liquid chromatography; NMR: Nuclear magnetic (3), 3,7,11-cembreriene-2,15-diol (4), 11,12-epoxy-Sarcophytol A (5), and resonance; IT-TOF: Ion trap-time of flight; MTT: 3-(4,5-dimethylthiazol-2-yl)-2; sarcophytol A (6).