After Ketsana Typhoon
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Juvenile Trapezia Spp. Crabs Can Increase Juvenile Host Coral Survival by Protection from Predation
Vol. 515: 151–159, 2014 MARINE ECOLOGY PROGRESS SERIES Published November 18 doi: 10.3354/meps10970 Mar Ecol Prog Ser Juvenile Trapezia spp. crabs can increase juvenile host coral survival by protection from predation H. Rouzé1,2,*, G. Lecellier1,2,3, S. C. Mills2,4, S. Planes1,2, V. Berteaux-Lecellier1,2, H. Stewart1,5 1CRIOBE USR 3278 CNRS-EPHE-UPVD, BP 1013, Moorea, 98729 French Polynesia 2Laboratoire d’Excellence ‘CORAIL’, 58 avenue Paul Alduy, 66860 Perpignan, France 3Université de Versailles-Saint Quentin, 55 Avenue de Paris, Versailles Cedex, France 4CRIOBE USR 3278 CNRS-EPHE-UPVD, 58 Avenue Paul Alduy, 66860 Perpignan Cedex, France 5Department of Fisheries and Oceans Canada, 4160 Marine Drive, West Vancouver, British Columbia V7V 1N6, Canada ABSTRACT:Adult crabs are known to play critical roles in the survival of their adult coral hosts, but little is known of the mutualism between juvenile crabs (≤0.5 cm) and their juvenile hosts. Field and laboratory experiments both demonstrated that the presence of juvenile crabs of the genus Trapezia in young host Pocillopora corals (2 to 3 cm diameter) increased coral survival by 32% and reduced consumption by the corallivorous seastar Acanthaster planci. These experi- ments also showed that juvenile Trapezia were not effective at deterring predation by another common predatory seastar, Culcita novaeguineae. Finally, our work highlights that the defensive ability of symbiotic crabs may be genus-specific, as juvenile Tetralia spp. crabs, obligate sym- bionts of Acropora spp., displayed no protection against either A. planci or C. novaeguineae. KEY WORDS: Juvenile · Trapeziid · Corals · Acanthaster planci · Culcita novaeguineae · Mutualism · Predation · Defence Resale or republication not permitted without written consent of the publisher INTRODUCTION fered the highest predation around Moorea (Leray et al. -
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. -
The Sea Stars (Echinodermata: Asteroidea): Their Biology, Ecology, Evolution and Utilization OPEN ACCESS
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/328063815 The Sea Stars (Echinodermata: Asteroidea): Their Biology, Ecology, Evolution and Utilization OPEN ACCESS Article · January 2018 CITATIONS READS 0 6 5 authors, including: Ferdinard Olisa Megwalu World Fisheries University @Pukyong National University (wfu.pknu.ackr) 3 PUBLICATIONS 0 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Population Dynamics. View project All content following this page was uploaded by Ferdinard Olisa Megwalu on 04 October 2018. The user has requested enhancement of the downloaded file. Review Article Published: 17 Sep, 2018 SF Journal of Biotechnology and Biomedical Engineering The Sea Stars (Echinodermata: Asteroidea): Their Biology, Ecology, Evolution and Utilization Rahman MA1*, Molla MHR1, Megwalu FO1, Asare OE1, Tchoundi A1, Shaikh MM1 and Jahan B2 1World Fisheries University Pilot Programme, Pukyong National University (PKNU), Nam-gu, Busan, Korea 2Biotechnology and Genetic Engineering Discipline, Khulna University, Khulna, Bangladesh Abstract The Sea stars (Asteroidea: Echinodermata) are comprising of a large and diverse groups of sessile marine invertebrates having seven extant orders such as Brisingida, Forcipulatida, Notomyotida, Paxillosida, Spinulosida, Valvatida and Velatida and two extinct one such as Calliasterellidae and Trichasteropsida. Around 1,500 living species of starfish occur on the seabed in all the world's oceans, from the tropics to subzero polar waters. They are found from the intertidal zone down to abyssal depths, 6,000m below the surface. Starfish typically have a central disc and five arms, though some species have a larger number of arms. The aboral or upper surface may be smooth, granular or spiny, and is covered with overlapping plates. -
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 ................................................................................................... -
Coral Reef Algae
Coral Reef Algae Peggy Fong and Valerie J. Paul Abstract Benthic macroalgae, or “seaweeds,” are key mem- 1 Importance of Coral Reef Algae bers of coral reef communities that provide vital ecological functions such as stabilization of reef structure, production Coral reefs are one of the most diverse and productive eco- of tropical sands, nutrient retention and recycling, primary systems on the planet, forming heterogeneous habitats that production, and trophic support. Macroalgae of an astonish- serve as important sources of primary production within ing range of diversity, abundance, and morphological form provide these equally diverse ecological functions. Marine tropical marine environments (Odum and Odum 1955; macroalgae are a functional rather than phylogenetic group Connell 1978). Coral reefs are located along the coastlines of comprised of members from two Kingdoms and at least over 100 countries and provide a variety of ecosystem goods four major Phyla. Structurally, coral reef macroalgae range and services. Reefs serve as a major food source for many from simple chains of prokaryotic cells to upright vine-like developing nations, provide barriers to high wave action that rockweeds with complex internal structures analogous to buffer coastlines and beaches from erosion, and supply an vascular plants. There is abundant evidence that the his- important revenue base for local economies through fishing torical state of coral reef algal communities was dominance and recreational activities (Odgen 1997). by encrusting and turf-forming macroalgae, yet over the Benthic algae are key members of coral reef communities last few decades upright and more fleshy macroalgae have (Fig. 1) that provide vital ecological functions such as stabili- proliferated across all areas and zones of reefs with increas- zation of reef structure, production of tropical sands, nutrient ing frequency and abundance. -
Vietnamese Reef-Building Corals and Reefs in the Open Part of the South China Sea
id15204125 pdfMachine by Broadgun Software - a great PDF writer! - a great PDF creator! - http://www.pdfmachine.com http://www.broadgun.com ISSN : 0974 - 7532 Volume 6 Issue 10 Research & Reviews in Trade Science Inc. BBiiooSScciieenncceess Regular Paper RRBS, 6(10), 2012 [288-296] Vietnamese reef-building corals and reefs in the open part of the South China Sea Yu.Ya.Latypov A. V. Zhirmunsky Institute of Marine Biology, Far Eastern Branch, Russian Academy of Sciences, Vladivostok-690041, (RUSSIA) E-mail : [email protected] Received: 5th July, 2012 ; Accepted: 21st September, 2012 ABSTRACT KEYWORDS The work analyzes and discusses survey results for Vietnamese reefs in South China Sea; the open part of the South China Sea. It shows the degree of exploration Reefs; and species composition of reef-building scleractinian of this region. It Reef-building scleractinian; has been determined that reefs and coral fauna residing on them have Species composition. similar characteristics and high species similarity by the coral composi- tion with other regions of Vietnam, and constitute a uniform complex of species in the equatorial zone of the Indo-Pacific region. Six species of scleractinian that have not been previously noticed at the reefs of Vietnam – were found Acropora abrolhosensis, A. insignis, A. parilis, Stylophora subseriata, Merulina scabricula, Pachyseris gemmae. 2012 Trade Science Inc. - INDIA INTRODUCTION geomorphic and climatic conditions includes factors dis- tinctly defining division of Vietnamese adjacent reefs into Vietnamese reef-building corals form various reef two types (figure 1). structures along the sea shore and around the islands. They are small adjacent reefs edging the sea shore, bar- rier reefs separated from the mainland (the island of Re and Jiang Bo reef) and atolls (Spratly Islands) in the open part of the South China Sea[1-3]. -
Zool({)Jgic/Ffll :§!L[Lj}Djj(F)§
Zoological Studies 34(2): 117-125 (1995) Zool({)JgiC/ffll :§!l[lJ}dJj(f)§ Distribution of Spirobranchus giganteus cornicuiatus (Hove) on the Coral Reefs of Southern Taiwan Chang-Feng Dai* and Hsiao-Pei Yang Institute of Oceanography, National Taiwan University, Taipei, Taiwan 106, R.O.C. (Accepted February 27, 1995) Chang-Feng Dai and Hsiao-Pei Yang (1995) Distribution of Spirobranchus giganteus corniculatus (Hove) on the coral reefs of southern Taiwan. Zoological Studies 34(2): 117-125. The distribution of Spirobranchus giganteus corniculatus (Hove), a widely distributed tube-building serpulid, on the coral reefs of southern Taiwan was studied by the transect sampling method. Two reef sites in Nanwan Bay, one with a high degree of physical disturbance and the other with a lower degree of disturbance, were surveyed. The spatial distri bution of S. giganteus corniculatus on coral colonies was also analyzed using distance to nearest neighbor. The results show that S. giganteus corniculatus is distributed nonrandomly among coral species. Four species, Porites tutee, P. lobete, P. lichen, Montipora informis, are frequently colonized by the worm. About 30 species are occasionally colonized and many coral species are not colonized. Coral species which are frequently colonized by the worm are competitively subordinate. The spatial distribution of S. giganteus corniculatus on a coral colony is related to the number of worms with a tendency toward clustering with in creasing number of worms per colony. In addition, most worms were found at intermediate depths (6-17 rn) where the reef surface was flat and there were more colonizable scleractinians. The distribution and abun dance of S. -
Wallace Et Al MTQ Catalogue Embedded Pics.Vp
Memoirs of the Queensland Museum | Nature 57 Revision and catalogue of worldwide staghorn corals Acropora and Isopora (Scleractinia: Acroporidae) in the Museum of Tropical Queensland Carden C. Wallace, Barbara J. Done & Paul R. Muir © Queensland Museum PO Box 3300, South Brisbane 4101, Australia Phone 06 7 3840 7555 Fax 06 7 3846 1226 Email [email protected] Website www.qm.qld.gov.au National Library of Australia card number ISSN 0079-8835 NOTE Papers published in this volume and in all previous volumes of the Memoirs of the Queensland Museum may be reproduced for scientific research, individual study or other educational purposes. Properly acknowledged quotations may be made but queries regarding the republication of any papers should be addressed to the Director. Copies of the journal can be purchased from the Queensland Museum Shop. A Guide to Authors is displayed at the Queensland Museum web site www.qm.qld.gov.au A Queensland Government Project Typeset at the Queensland Museum Memoirs of the Queensland Museum | Nature Volume 57 Minister: The Honourable Ros Bates, MP, Minister for Science, Information Technology, Innovation and the Arts CEO: I.D. Galloway, PhD Editor in Chief: J.N.A. Hooper, PhD Managing Editor: S.M. Verschoore Issue Editor: P.J.F. Davie PUBLISHED BY ORDER OF THE BOARD 30 JUNE 2012 © The State of Queensland (Queensland Museum), 2012 PO Box 3300, South Brisbane 4101, Qld Australia Phone 61 7 3840 7555 Fax 61 7 3846 1226 www.qm.qld.gov.au National Library of Australia card number ISSN 0079-8835 COVER: Acropora muricata (Linnaeus, 1758), type species of Acropora, Maldives, 2006 (MTQ-G60372), photo: Paul Muir. -
AC26 Doc. 20 Annex 6 English Only / Únicamente En Inglés / Seulement En Anglais
AC26 Doc. 20 Annex 6 English only / únicamente en inglés / seulement en anglais Annex 6 CORAL SPECIES, SYNONYMS, AND NOMENCLATURE REFERENCES CURRENTLY RECOGNIZED IN THE UNEP-WCMC DATABASE Data kindly provided by UNEP-WCMC AC26 Doc. 20, Annex 6 – 1 AC26 Doc. 20 Annex 6 English only / únicamente en inglés / seulement en anglais CORAL SPECIES AND SYNONYMS CURRENTLY RECOGNIZED IN THE UNEP‐WCMC DATABASE 1. Scleractinia families FamName Accepted Name SpcAuthor Nomenclature Reference Synonyms ACROPORIDAE Acropora abrolhosensis Veron, 1985 Veron (2000) Acropora mangarevensis; Madrepora ACROPORIDAE Acropora abrotanoides (Lamarck, 1816) Veron (2000) crassa; Madrepora abrotanoides ACROPORIDAE Acropora aculeus (Dana, 1846) Veron (2000) Madrepora aculeus Acropora diffusa; Madrepora acuminata; ACROPORIDAE Acropora acuminata (Verrill, 1864) Veron (2000) Madrepora diffusa; Madrepora nigra ACROPORIDAE Acropora akajimensis Veron, 1990 Veron (2000) Madrepora anthocercis; Madrepora ACROPORIDAE Acropora anthocercis (Brook, 1893) Veron (2000) coronata ACROPORIDAE Acropora arabensis Hodgson & Carpenter, 1995 Veron (2000) Acropora cribripora; Acropora hebes; Acropora manni; Acropora yaeyamaensis; ACROPORIDAE Acropora aspera (Dana, 1846) Veron (2000) Madrepora aspera; Madrepora cribripora; Madrepora hebes; Madrepora manni ACROPORIDAE Acropora austera (Dana, 1846) Veron (2000) Madrepora austera ACROPORIDAE Acropora awi Wallace & Wolstenholme, 1998 Veron (2000) ACROPORIDAE Acropora azurea Veron & Wallace, 1984 Veron (2000) ACROPORIDAE Acropora batunai Wallace, -
SEASMART Program Final Report Annex
Creating a Sustainable, Equitable & Affordable Marine Aquarium Industry in Papua New Guinea | 1 Table of Contents Executive Summary ............................................................................................................ 7 Introduction ....................................................................................................................... 15 Contract Deliverables ........................................................................................................ 21 Overview of PNG in the Marine Aquarium Trade ............................................................. 23 History of the Global Marine Aquarium Trade & PNG ............................................ 23 Extent of the Global Marine Aquarium Trade .......................................................... 25 Brief History of Two Other Coastal Fisheries in PNG ............................................ 25 Destructive Potential of an Inequitable, Poorly Monitored & Managed Nature of the Trade Marine Aquarium Fishery in PNG ........................... 26 Benefit Potential of a Well Monitored & Branded Marine Aquarium Trade (and Other Artisanal Fisheries) in PNG ................................................................... 27 PNG Way to Best Business Practice & the Need for Effective Branding .............. 29 Economic & Environmental Benefits....................................................................... 30 Competitive Advantages of PNG in the Marine Aquarium Trade ................................... 32 Pristine Marine -
Northwestern Hawaiian Islands/Kure Atoll Assessment and Monitoring Program
Northwestern Hawaiian Islands/Kure Atoll Assessment and Monitoring Program Final Report March 2002 Grant Number NA070A0457 William j. Walsh1, Ryan Okano2, Robert Nishimoto1, Brent Carman1. 1 Division of Aquatic Resources 1151 Punchbowl Street Rm. 330 Honolulu, HI 96813 2 Botany Department University of Hawai`i Mānoa Honolulu, HI 96822 2 INTRODUCTION The Northwest Hawaiian Islands (NWHI) consist of 9,124 km2 of land and approximately 13,000 km2 of coral reef habitat. They comprise 70% of all coral reef areas under U.S. jurisdiction. This isolated archipelago of small islands, atolls, reefs and banks represent a unique and largely pristine coral reef ecosystem. The islands support millions of nesting seabirds and are breeding grounds for the critically endangered Hawaiian monk seal and threatened green sea turtle. The reefs include a wide range of habitats and support a diverse assemblage of indigenous and endemic reef species, many of which have yet to be described. Kure Atoll, located at the northwestern end of the NWHI chain (approximately 28º 25’ N latitude and 178º 20’ W longitude) is the northernmost atoll in the world. The atoll is located 91 km northwest of Midway Islands and nearly 1,958 km northwest of Honolulu. It is a nearly circular atoll with a diameter of 10 km (6mi). The outer reef is continuous Figure 1. IKONOS satellite image of Kure Atoll 3 and almost encircles the atoll’s lagoon except for passages to the southwest (Fig. 1). An emergent rock ledge consisting primarily of coralline algae and algally bound and encrusted coral is present along some sections of the reef crest.