Abundance of Giant Clam in Coral Reef Ecosystem at Pari Island: a Population Comparison of 2003'S to 1984'S Data
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Review of Selected Species Subject to Long- Standing Import Suspensions
UNEP-WCMC technical report Review of selected species subject to long- standing import suspensions Part II: Asia and Oceania (Version edited for public release) Review of selected species subject to long-standing import suspensions. Part II: Asia and Oceania Prepared for The European Commission, Directorate General Environment, Directorate E - Global & Regional Challenges, LIFE ENV.E.2. – Global Sustainability, Trade & Multilateral Agreements, Brussels, Belgium Prepared February 2016 Copyright European Commission 2016 Citation UNEP-WCMC. 2016. Review of selected species subject to long-standing import suspensions. Part II: Asia and Oceania. UNEP-WCMC, Cambridge. The UNEP World Conservation Monitoring Centre (UNEP-WCMC) is the specialist biodiversity assessment of the United Nations Environment Programme, the world’s foremost intergovernmental environmental organization. The Centre has been in operation for over 30 years, combining scientific research with policy advice and the development of decision tools. We are able to provide objective, scientifically rigorous products and services to help decision- makers recognize the value of biodiversity and apply this knowledge to all that they do. To do this, we collate and verify data on biodiversity and ecosystem services that we analyze and interpret in comprehensive assessments, making the results available in appropriate forms for national and international level decision-makers and businesses. To ensure that our work is both sustainable and equitable we seek to build the capacity of partners -
Tridacna Maxima (Reding), and Hippopus Hippopus (Linnaeus)!
Pacific Science (1976), Vol. 30, No.3, p. 219-233 Printed in Great Britain Early Life History of the Giant Clams Tridacna crocea Lamarck, Tridacna maxima (Reding), and Hippopus hippopus (Linnaeus)! STEPHEN C. JAMESON2 ABST RACT: Giant clams may be stimulated to spawn by the addition of macer ated gonads to the water.Individuals of Tridacna maxima collected at Anae Island, Guam, spawned from N ovember to March. On Palau, Hippopus hippopus spawned in June and Tridacna crocea, in July. Tridacna crocea, T. maxima, and H. hippopus displayed a stereotype d develop ment pattern in morphogenesis and rate of development . Fertilized eggs of T. crocea, T . maxima, and H. hippopus had mean diameters of 93.1, 104.5, and 130.0 psx», respectively . The day-2 straight-hinge veligers of T . crocea, T . maxima, and H. hippopus had mean shell lengths of 155.0, 168.0, and 174.4 pm, respec tively. Settlement occurred 12, 11, and 9 days after fertili zation at a mean shell length of 168.0, 195.0, and 202.0 pm for T . crocea,T . max ima, and H. bippopss, respectively. Metamorphosis was basically complete about 1 day after settlement. Juveniles of T . crocea, T. max ima, and H. hippopus first acqui re zooxanthellae after 19, 21, and 25 days, respectively. Growth rates increase sharply after the acquisition of zoo xanthellae. Juvenile shells show first signs of becoming opaque after 47 days for T . maxima and after 50 days for H. hippopus. G rANT CLAMS are protandric fun ctional herma formation, and initial organogenesis. The larval phrodites (Wada 1942, 1952). -
The Ecological Significance of Giant Clams in Coral Reef Ecosystems
Biological Conservation 181 (2015) 111–123 Contents lists available at ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/biocon Review The ecological significance of giant clams in coral reef ecosystems ⇑ Mei Lin Neo a,b, William Eckman a, Kareen Vicentuan a,b, Serena L.-M. Teo b, Peter A. Todd a, a Experimental Marine Ecology Laboratory, Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, Singapore 117543, Singapore b Tropical Marine Science Institute, National University of Singapore, 18 Kent Ridge Road, Singapore 119227, Singapore article info abstract Article history: Giant clams (Hippopus and Tridacna species) are thought to play various ecological roles in coral reef Received 14 May 2014 ecosystems, but most of these have not previously been quantified. Using data from the literature and Received in revised form 29 October 2014 our own studies we elucidate the ecological functions of giant clams. We show how their tissues are food Accepted 2 November 2014 for a wide array of predators and scavengers, while their discharges of live zooxanthellae, faeces, and Available online 5 December 2014 gametes are eaten by opportunistic feeders. The shells of giant clams provide substrate for colonization by epibionts, while commensal and ectoparasitic organisms live within their mantle cavities. Giant clams Keywords: increase the topographic heterogeneity of the reef, act as reservoirs of zooxanthellae (Symbiodinium spp.), Carbonate budgets and also potentially counteract eutrophication via water filtering. Finally, dense populations of giant Conservation Epibiota clams produce large quantities of calcium carbonate shell material that are eventually incorporated into Eutrophication the reef framework. Unfortunately, giant clams are under great pressure from overfishing and extirpa- Giant clams tions are likely to be detrimental to coral reefs. -
Taxonomy of Indonesian Giant Clams (Cardiidae, Tridacninae)
BIODIVERSITAS ISSN: 1412-033X Volume 13, Number 3, July 2012 E-ISSN: 2085-4722 Pages: 118-123 DOI: 10.13057/biodiv/d130303 Taxonomy of Indonesian giant clams (Cardiidae, Tridacninae) UDHI EKO HERNAWAN♥ Biotic Conservation Area of Tual Sea, Research Center for Oceanography, Indonesian Institute of Sciences. Jl. Merdeka, Katdek Tual, Southeast Maluku 97611. Tel. +92-916-23839, Fax. +62-916-23873, ♥email: [email protected] Manuscript received: 20 December 2010. Revision accepted: 20 June 2011. ABSTRACT Hernawan E. 2012. Taxonomy of Indonesian giant clams (Cardiidae, Tridacninae). Biodiversitas 13: 118-123. A taxonomic study was conducted on the giant clam’s specimens deposited in Museum Zoologicum Bogoriense (MZB), Cibinong Indonesia. Taxonomic overviews of the examined specimens are given with diagnostic characters, remarks, habitat and distribution. Discussion is focused on specific characters distinguishing each species. From seven species known to distribute in Indonesian waters, there are six species, Tridacna squamosa Lamarck, 1819; T. gigas Linnaeus, 1758; T. derasa Roding, 1798; T. crocea Lamarck, 1819; T. maxima Roding,1798; and Hippopus hippopus Linnaeus, 1758. This study suggests the need for collecting specimen of H. porcellanus Rosewater, 1982. Important characters to distinguish species among Tridacninae are interlocking teeth on byssal orifice, life habits, presence of scales and inhalant siphon tentacles. Key words: Tridacninae, taxonomy, Museum Zoologicum Bogoriense INTRODUCTION family (Tridacnidae) or revised to be subfamily Tridacninae, included in family Cardiidae. Recently, based Giant clams, the largest bivalve in the world, occur on sperm ultrastructure and molecular phylogenetic studies, naturally in association with coral reefs throughout the the clams are belonging to family Cardiidae, subfamily tropical and subtropical waters of the Indo-Pacific region. -
Giant Clams (Bivalvia : Cardiidae : Tridacninae)
Oceanography and Marine Biology: An Annual Review, 2017, 55, 87-388 © S. J. Hawkins, D. J. Hughes, I. P. Smith, A. C. Dale, L. B. Firth, and A. J. Evans, Editors Taylor & Francis GIANT CLAMS (BIVALVIA: CARDIIDAE: TRIDACNINAE): A COMPREHENSIVE UPDATE OF SPECIES AND THEIR DISTRIBUTION, CURRENT THREATS AND CONSERVATION STATUS MEI LIN NEO1,11*, COLETTE C.C. WABNITZ2,3, RICHARD D. BRALEY4, GERALD A. HESLINGA5, CÉCILE FAUVELOT6, SIMON VAN WYNSBERGE7, SERGE ANDRÉFOUËT6, CHARLES WATERS8, AILEEN SHAU-HWAI TAN9, EDGARDO D. GOMEZ10, MARK J. COSTELLO8 & PETER A. TODD11* 1St. John’s Island National Marine Laboratory, c/o Tropical Marine Science Institute, National University of Singapore, 18 Kent Ridge Road, Singapore 119227, Singapore 2The Pacific Community (SPC), BPD5, 98800 Noumea, New Caledonia 3Changing Ocean Research Unit, Institute for the Oceans and Fisheries, The University of British Columbia, AERL, 2202 Main Mall, Vancouver, BC, Canada 4Aquasearch, 6–10 Elena Street, Nelly Bay, Magnetic Island, Queensland 4819, Australia 5Indo-Pacific Sea Farms, P.O. Box 1206, Kailua-Kona, HI 96745, Hawaii, USA 6UMR ENTROPIE Institut de Recherche pour le développement, Université de La Réunion, CNRS; Centre IRD de Noumea, BPA5, 98848 Noumea Cedex, New Caledonia 7UMR ENTROPIE Institut de Recherche pour le développement, Université de La Réunion, CNRS; Centre IRD de Tahiti, BP529, 98713 Papeete, Tahiti, French Polynesia 8Institute of Marine Science, University of Auckland, P. Bag 92019, Auckland 1142, New Zealand 9School of Biological Sciences, Universiti Sains Malaysia, Penang 11800, Malaysia 10Marine Science Institute, University of the Philippines, Diliman, Velasquez Street, Quezon City 1101, Philippines 11Experimental Marine Ecology Laboratory, Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, Singapore 117557, Singapore *Corresponding authors: Mei Lin Neo e-mail: [email protected] Peter A. -
Prioritized Species for Mariculture in India
Prioritized Species for Mariculture in India Compiled & Edited by Ritesh Ranjan Muktha M Shubhadeep Ghosh A Gopalakrishnan G Gopakumar Imelda Joseph ICAR - Central Marine Fisheries Research Institute Post Box No. 1603, Ernakulam North P.O. Kochi – 682 018, Kerala, India www.cmfri.org.in 2017 Prioritized Species for Mariculture in India Published by: Dr. A Gopalakrishnan Director ICAR - Central Marine Fisheries Research Institute Post Box No. 1603, Ernakulam North P.O. Kochi – 682 018, Kerala, India www.cmfri.org.in Email: [email protected] Tel. No.: +91-0484-2394867 Fax No.: +91-0484-2394909 Designed at G.K. Print House Pvt. Ltd. Rednam Gardens Visakhapatnam- 530002, Andhra Pradesh Cell: +91 9848196095, www.gkprinthouse.com Cover page design: Abhilash P. R., CMFRI, Kochi Illustrations: David K. M., CMFRI, Kochi Publication, Production & Co-ordination: Library & Documentation Centre, CMFRI Printed on: November 2017 ISBN 978-93-82263-14-2 © 2017 ICAR - Central Marine Fisheries Research Institute, Kochi All rights reserved. Material contained in this publication may not be reproduced in any form without the permission of the publisher. Citation : Ranjan, R., Muktha, M., Ghosh, S., Gopalakrishnan, A., Gopakumar, G. and Joseph, I. (Eds.). 2017. Prioritized Species for Mariculture in India. ICAR-CMFRI, Kochi. 450 pp. CONTENTS Foreword ................................................................................................................. i Preface ................................................................................................................. -
PETITION to LIST the TRIDACNINAE GIANT CLAMS (Excluding Tridacna Rosewateri) AS THREATENED OR ENDANGERED UNDER the ENDANGERED SPECIES ACT
PETITION TO LIST THE TRIDACNINAE GIANT CLAMS (excluding Tridacna rosewateri) AS THREATENED OR ENDANGERED UNDER THE ENDANGERED SPECIES ACT Dwayne W. Meadows, Ph.D. 9063 Dunloggin Rd. Ellicott City, MD 21042 Non-official communication of interest Giant Clam Petition 1 NOTICE OF PETITION 7 August 2016 Donna Wieting, Director Office of Protected Resources, F/PROD National Marine Fisheries Service 1315 East West Highway Silver Spring, MD 20910 [email protected] Dear Ms. Wieting, Pursuant to section 4(b) of the Endangered Species Act (“ESA”), 16 U.S.C. § 1533(b), section 553(3) of the Administrative Procedure Act, 5 U.S.C. § 553(e), and 50 CFR 424.14(a), Dwayne W. Meadows, Ph.D. hereby petitions the Secretary of Commerce, through the National Marine Fisheries Service (“NMFS”, the lead office for implementing the ESA), to list the Tridacninae Giant Clams (excluding Tridacna rosewateri) as a threatened or endangered species under the ESA (16 U.S.C. §§ 1531 et seq.) throughout all or a significant portion of their ranges. Tridacna rosewateri occurs only in Mauritius and there is no additional information on the status of this species, so it is not considered further as part of this petition. NMFS has jurisdiction over this petition because the petitioned species are marine. This petition sets in motion a specific process, placing definite response requirements on NMFS. Specifically, NMFS must issue an initial finding as to whether this petition “presents substantial scientific or commercial information indicating that the petitioned action may be warranted.” 16 U.S.C. § 1533(b)(3)(A). NMFS must make this initial finding “[t]o the maximum extent practicable, within 90 days after receiving the petition.” Id. -
Calculating the Contribution of Zooxanthellae to Giant Clams Respiration Energy Requirements
Journal of Coastal Development ISSN: 1410-5217 Volume 5, Number 3, June 2002 : 101-110 Accredited: 69/Dikti/Kep/2000 Review CALCULATING THE CONTRIBUTION OF ZOOXANTHELLAE TO GIANT CLAMS RESPIRATION ENERGY REQUIREMENTS Ambariyanto*) Marine Science Department, Faculty of Fisheries and Marine Sciences, Diponegoro University, Semarang Indonesia. Email: [email protected] Received: April 24, 2002 ; Accepted: May 27, 2002 ABSTRACT Giant clams (Tridacnidae) are known to live in association with photosynthetic single cell dinoflagellate algae commonly called zooxanthellae. These algae which can be found in the mantle of the clams are capable of transferring part of their photosynthates which become an important source of energy to the host ( apart from filter feeding activity). In order to understand the basic biological processes of the giant clams , the contribution of zooxanthellae to the clam’s energy requirement need to be determined. This review describes how to calculate the contribution of zooxanthellae to the giant clam’s energy requirement for the respiration process. Key words: Giant clams, tridacnidae, zooxanthellae CZAR *) Correspondence: Tel. 024-7474698, Fax. 024-7474698, Email: [email protected] INTRODUCTION One of the important aspects of the biology of giant clams is the existence Giant clams (Family: Tridacnidae) are of zooxanthellae which occupy the mantle large bivalves that are commonly found in of the clams as endosymbiotic coral reef habitats especially in the Indo- dinoflagellate algae (Lucas, 1988). These Pacific region. This family consists of two zooxanthellae have a significant role, genera (Tridacna and Hippopus) and eight especially in the energy requirements of species: Tridacna gigas, T. derasa, T. giant clams, since they are capable of squamosa, T. -
Giant Clams1
CHAPTER 13 Giant Clams1 John L. Munro I. INTRODUCTION In the past decade there has been an enormous upsurge in interest in the giant clams (Family Tridacnidae), resulting largely from the realization that their artificial propagation is technically feasible (La Barbera, 1975; Jameson, 1976; Beckvar, 1981; Gwyther and Munro, 1981), that growth rates of the larger species are relatively rapid (Munro and Gwyther, 1981) and that, by virtue of their symbiotic relationship with a species or species group of dinoflagellate algae,theyaretheworld'sonlyself-feedingfarmanimals(Munro, 1983). These factors combined with the realization that stocks of the larger species had been dramatically depleted in most parts of the South Pacific, both by poachers intent on supplying the lucrative Taiwanese market for giant clam adductor muscle and by continuing local harvests by expanding populations of South Pacific Island ers, led to a number of research projects being launched at various institutions in the region; notably at the University of Papua New Guinea and the Micronesian Mariculture Demonstration Center in Palau (both in 1976), by the International Center for Living Aquatic Resources Management (ICLARM) in 1983 and by the Australian Center for International Agricultural Research (ACIAR) in 1984. As a result of these collective efforts, there is a substantial body of informa tion available on many aspects of the biology and ecology of giant clams and a reasonable understanding of the factors which constrain the intensive harvesting of giant clam stocks for commercial or subsistence purposes. It is now techni cally feasible to spawn routinely mature giant clams and raise the larvae through their juvenile stages to maturity (Heslinga and Fitt, 1987). -
Giant Clams by John L. Munro FFA Report 92/75
Giant Clams By John L. Munro FFA Report 92/75 PACIFIC ISLANDS FORUM FISHERIES AGENCY P.O.BOX 629 HONIARA SOLOMON ISLANDS TELEPHONE (677) 21124 FAX (677) 23995 WEB http://www.ffa.int Giant Clam CHAPTER 13 Giant Clams1 by John L. Munro I. INTRODUCTION In the past decade there has been an enormous upsurge in interest in the giant clams (Family Tridacnidae), resulting largely from the realization that their artificial propagation is technically feasible (La Barbera, 1975; Jameson, 1976; Beckvar, 1981; Gwyther and Munro, 1981), that growth rates of the larger species are relatively rapid (Munro and Gwyther, 1981) and that by virtue of their symbiotic relationship with a species or species group of dinoflagellate algae they are the world's only self-feeding farm animals (Munro, 1983). These factors combined with the realization that stocks of the larger species had been dramatically depleted in most parts of the South Pacific, both by poachers intent on supplying the lucrative Taiwanese market for giant clam adductor muscle, and by continuing local harvests by expanding populations of South Pacific Islanders, led to a number of research projects being launched at various institutions in the Region; notably at the University of Papua New Guinea and the Micronesian Mariculture Demonstration Center in Palau (both in 1976), by the International Center for Living Aquatic Resources Management (ICLARM) in 1983 and by the Australian Center for International Agricultural Research (ACIAR) in 1984. As a result of these collective efforts there is a substantial body of information available on many aspects of the biology and ecology of giant clams and a reasonable understanding of the factors which constrain the intensive harvesting of giant clam stocks for commercial or subsistence purposes. -
Identifying Robust Proxies of Gonad Maturation for the Protandrous Hermaphrodite Tridacna Maxima (Röding, 1798, Bivalvia) From
Identifying Robust Proxies of Gonad Maturation for the Protandrous Hermaphrodite Tridacna maxima (Röding, 1798, Bivalvia) from Individual to Population Scale Mathilde Menoud, Simon Van Wynsberge, Gilles Le Moullac, Peva Levy, Serge Andréfouët, Georges Remoissenet, Nabila Gaertner-Mazouni To cite this version: Mathilde Menoud, Simon Van Wynsberge, Gilles Le Moullac, Peva Levy, Serge Andréfouët, et al.. Identifying Robust Proxies of Gonad Maturation for the Protandrous Hermaphrodite Tridacna maxima (Röding, 1798, Bivalvia) from Individual to Population Scale. Journal of Shellfish Research, National Shellfisheries Association, 2016, 35 (1), pp.51 - 61. 10.2983/035.035.0107. hal-01613648 HAL Id: hal-01613648 https://hal.archives-ouvertes.fr/hal-01613648 Submitted on 9 Oct 2017 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. Journal of Shellfish Research, Vol. 35, No. 1, 51–61, 2016. IDENTIFYING ROBUST PROXIES OF GONAD MATURATION FOR THE PROTANDROUS HERMAPHRODITE TRIDACNA MAXIMA (RODING,€ 1798, BIVALVIA) FROM INDIVIDUAL TO POPULATION SCALE MATHILDE MENOUD,1,2 -
Tridacna Spp. and Hippopus Hippopus in the Philippines Using Mitochondrial CO1 and 16S Rrna Genes
ARTICLE Updates on the status of giant clams Tridacna spp. and Hippopus hippopus in the Philippines using mitochondrial CO1 and 16S rRNA genes Apollo Marco D. Lizano1,2 and Mudjekeewis D. Santos1* 1Genetic Fingerprinting Laboratory, Marine Fisheries Research Division, 1National Fisheries Research and Development Institute 2The Marine Science Institute University of the Philippines, Diliman Quezon City, Philippines he CO1 and 16S rRNA genes of six of the possible tion site at 367-370 bp (5’AGCT3’) for the species of T. maxima eight species of giant clams (Hippopus hippopus, as opposed to the species of Tridacna sp. YCT-2005. Alu I re- Tridacna gigas, T. crocea, T. squamosa, T. derasa, striction endonuclease was identified as a candidate diagnostic and Tridacna sp.YCT-2005) under the Tridacnidae enzyme to differentiate between these species. This study con- family found in the Philippines were sequenced for firmed the identity of giant clams found in the Philippines using Tmolecular approach -based species identification. We first report- molecular techniques. The use of DNA barcoding can be a useful ed here the CO1 sequence of H. hippopus and made it available tool to identify different species of giant clams which is needed online through GenBank. We also reported the first sighting of for their proper management and conservation in the Philippines, Tridacna sp. YCT-2005 in Philippine waters, an undescribed since they are all declared as endangered. species of giant clam, which has initially been reported to be a potentially new species that was thought to be found only in Tai- INTRODUCTION wan. Phylogenetic trees of CO1 and 16S rRNA gene sequences of giant clam samples from the Philippines were constructed Giant clams are one of the world’s largest bivalves, ranging using both the Neighbor-Joining approach and the Maximum- from 15 cm for Tridacna crocea Lammarck 1819 to 150 cm for Likelihood approach.