Improving Management Effectiveness for the Marine Protected Areas of Rodrigues (Indian Ocean)
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Coral Reef Monitoring in Kofiau and Boo Islands Marine Protected Area, Raja Ampat, West Papua. 2009—2011
August 2012 Indo-Pacific Division Indonesia Report No 6/12 Coral Reef Monitoring in Kofiau and Boo Islands Marine Protected Area, Raja Ampat, West Papua. 2009—2011 Report Compiled By: Purwanto, Muhajir, Joanne Wilson, Rizya Ardiwijaya, and Sangeeta Mangubhai August 2012 Indo-Pacific Division Indonesia Report No 6/12 Coral Reef Monitoring in Kofiau and Boo Islands Marine Protected Area, Raja Ampat, West Papua. 2009—2011 Report Compiled By: Purwanto, Muhajir, Joanne Wilson, Rizya Ardiwijaya, and Sangeeta Mangubhai Published by: TheNatureConservancy,Indo-PacificDivision Purwanto:TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur,Bali, Indonesia.Email: [email protected] Muhajir: TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur,Bali, Indonesia.Email: [email protected] JoanneWilson: TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur,Bali, Indonesia. RizyaArdiwijaya:TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur, Bali,Indonesia.Email: [email protected] SangeetaMangubhai: TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2, Sanur,Bali,Indonesia.Email: [email protected] Suggested Citation: Purwanto,Muhajir,Wilson,J.,Ardiwijaya,R.,Mangubhai,S.2012.CoralReefMonitoringinKofiau andBooIslandsMarineProtectedArea,RajaAmpat,WestPapua.2009-2011.TheNature Conservancy,Indo-PacificDivision,Indonesia.ReportN,6/12.50pp. © 2012012012201 222 The Nature Conservancy AllRightsReserved.Reproductionforanypurposeisprohibitedwithoutpriorpermission. AllmapsdesignedandcreatedbyMuhajir. CoverPhoto: -
Reef Coralgal Assemblages As Recorders of Paleobathymetry and Sea Level Changes in the Indo-Pacific Province
PERGAMON Quaternary Science Reviews 18 (1999) 1681-1695 QSR Reef coralgal assemblages as recorders of paleobathymetry and sea level changes in the Indo-Pacific province I' G. Cabioch">*,L.F. Montaggionib, G. Faurec, A. Ribaud-Lamentib "ORSTOM (L'Institut franqais de Recherche scientifique pour le Développement en Coopérationj, UMR 6526 'Géosciences Azur', B.P. A5, Noum& Cedex, New Caledonia '.:I bUPRESA CNRS 6019, Centre de Sédinientologie et Palhontologie, Université de Provence, 13331 Marseille Cedex 3, France 'UPRESA CNRS 6019, Laboratoire $Hydrobiologie A.larine et Continentale, Université des Sciences et Techniques du Languedoc, Place Eugène Bataillon, 34095 Montpellier Cedex 5, France æiP Abstract Science Ltd. All Eights reserved. - __ D l I Fonds Documentaire I R 1 I I 1 I O Il lull~Illi~~lÎ~~~~i~iipillill1002 1466 1. Introduction building coral communities, are regarded as- one of the most reliable sea-level markers (Liglity et al., 1978; During thellast few decades, our knowledge of psst- 1 Davies and Montaggioni, 1985; Hopley, 1986; Montag- glacial sea-level changes has been greatly enhanced gioni and Faure, 1997). through studies of reef sites (Fairbanks, 1989; Bard et al., Corals older than 6 ka BP are not generally directly 1990,1996; Chappell and Polach, 1991; Edwards et al., accessible from rapidly subsiding (e.g. intraplate volcanic 1993).The tropical zone offers the opportunity to exami- islands) or slowly uplifting coasts (e.g. hydro-isostasy- ne sea-level changes and the melting history of continen- experiencing areas). As a result, the only way to recover tal ice sheets far from the polar zones (Bard et al., 1996). -
Petition to List Eight Species of Pomacentrid Reef Fish, Including the Orange Clownfish and Seven Damselfish, As Threatened Or Endangered Under the U.S
BEFORE THE SECRETARY OF COMMERCE PETITION TO LIST EIGHT SPECIES OF POMACENTRID REEF FISH, INCLUDING THE ORANGE CLOWNFISH AND SEVEN DAMSELFISH, AS THREATENED OR ENDANGERED UNDER THE U.S. ENDANGERED SPECIES ACT Orange Clownfish (Amphiprion percula) photo by flickr user Jan Messersmith CENTER FOR BIOLOGICAL DIVERSITY SUBMITTED SEPTEMBER 13, 2012 Notice of Petition Rebecca M. Blank Acting Secretary of Commerce U.S. Department of Commerce 1401 Constitution Ave, NW Washington, D.C. 20230 Email: [email protected] Samuel Rauch Acting Assistant Administrator for Fisheries NOAA Fisheries National Oceanographic and Atmospheric Administration 1315 East-West Highway Silver Springs, MD 20910 E-mail: [email protected] PETITIONER Center for Biological Diversity 351 California Street, Suite 600 San Francisco, CA 94104 Tel: (415) 436-9682 _____________________ Date: September 13, 2012 Shaye Wolf, Ph.D. Miyoko Sakashita Center for Biological Diversity Pursuant to Section 4(b) of the Endangered Species Act (“ESA”), 16 U.S.C. § 1533(b), Section 553(3) of the Administrative Procedures Act, 5 U.S.C. § 553(e), and 50 C.F.R.§ 424.14(a), the Center for Biological Diversity hereby petitions the Secretary of Commerce and the National Oceanographic and Atmospheric Administration (“NOAA”), through the National Marine Fisheries Service (“NMFS” or “NOAA Fisheries”), to list eight pomacentrid reef fish and to designate critical habitat to ensure their survival. The Center for Biological Diversity (“Center”) is a non-profit, public interest environmental organization dedicated to the protection of imperiled species and their habitats through science, policy, and environmental law. The Center has more than 350,000 members and online activists throughout the United States. -
Community Structure and Biogeography of Shore Fishes in the Gulf of Aqaba, Red Sea
Helgol Mar Res (2002) 55:252–284 DOI 10.1007/s10152-001-0090-y ORIGINAL ARTICLE Maroof A. Khalaf · Marc Kochzius Community structure and biogeography of shore fishes in the Gulf of Aqaba, Red Sea Received: 2 April 2001 / Received in revised form: 2 November 2001 / Accepted: 2 November 2001 / Published online: 24 January 2002 © Springer-Verlag and AWI 2002 Abstract Shore fish community structure off the Jorda- Introduction nian Red Sea coast was determined on fringing coral reefs and in a seagrass-dominated bay at 6 m and 12 m Coral reefs are one of the most complex marine ecosys- depths. A total of 198 fish species belonging to 121 gen- tems in which fish communities reach their highest de- era and 43 families was recorded. Labridae and Poma- gree of diversity (Harmelin-Vivien 1989). Morphological centridae dominated the ichthyofauna in terms of species properties and the geographical region of the coral reef richness and Pomacentridae were most abundant. Nei- determine the structure of the fish assemblages (Sale ther diversity nor species richness was correlated to 1980; Thresher 1991; Williams 1991). The ichthyofauna depth. The abundance of fishes was higher at the deep of coral reefs can be linked to varying degrees with adja- reef slope, due to schooling planktivorous fishes. At cent habitats (Parrish 1989) such as seagrass meadows 12 m depth abundance of fishes at the seagrass-dominat- (Ogden 1980; Quinn and Ogden 1984; Roblee and ed site was higher than on the coral reefs. Multivariate Ziemann 1984; Kochzius 1999), algal beds (Rossier and analysis demonstrated a strong influence on the fish as- Kulbicki 2000) and mangroves (Birkeland 1985; Thollot semblages by depth and benthic habitat. -
"Red Sea and Western Indian Ocean Biogeography"
A review of contemporary patterns of endemism for shallow water reef fauna in the Red Sea Item Type Article Authors DiBattista, Joseph; Roberts, May B.; Bouwmeester, Jessica; Bowen, Brian W.; Coker, Darren James; Lozano-Cortés, Diego; Howard Choat, J.; Gaither, Michelle R.; Hobbs, Jean-Paul A.; Khalil, Maha T.; Kochzius, Marc; Myers, Robert F.; Paulay, Gustav; Robitzch Sierra, Vanessa S. N.; Saenz Agudelo, Pablo; Salas, Eva; Sinclair-Taylor, Tane; Toonen, Robert J.; Westneat, Mark W.; Williams, Suzanne T.; Berumen, Michael L. Citation A review of contemporary patterns of endemism for shallow water reef fauna in the Red Sea 2015:n/a Journal of Biogeography Eprint version Post-print DOI 10.1111/jbi.12649 Publisher Wiley Journal Journal of Biogeography Rights This is the peer reviewed version of the following article: DiBattista, J. D., Roberts, M. B., Bouwmeester, J., Bowen, B. W., Coker, D. J., Lozano-Cortés, D. F., Howard Choat, J., Gaither, M. R., Hobbs, J.-P. A., Khalil, M. T., Kochzius, M., Myers, R. F., Paulay, G., Robitzch, V. S. N., Saenz-Agudelo, P., Salas, E., Sinclair-Taylor, T. H., Toonen, R. J., Westneat, M. W., Williams, S. T. and Berumen, M. L. (2015), A review of contemporary patterns of endemism for shallow water reef fauna in the Red Sea. Journal of Biogeography., which has been published in final form at http:// doi.wiley.com/10.1111/jbi.12649. This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving. Download date 23/09/2021 15:38:13 Link to Item http://hdl.handle.net/10754/583300 1 Special Paper 2 For the virtual issue, "Red Sea and Western Indian Ocean Biogeography" 3 LRH: J. -
Hawai'i Institute of Marine Biology Northwestern Hawaiian Islands
Hawai‘i Institute of Marine Biology Northwestern Hawaiian Islands Coral Reef Research Partnership Quarterly Progress Reports II-III August, 2005-March, 2006 Report submitted by Malia Rivera and Jo-Ann Leong April 21, 2006 Photo credits: Front cover and back cover-reef at French Frigate Shoals. Upper left, reef at Pearl and Hermes. Photos by James Watt. Hawai‘i Institute of Marine Biology Northwestern Hawaiian Islands Coral Reef Research Partnership Quarterly Progress Reports II-III August, 2005-March, 2006 Report submitted by Malia Rivera and Jo-Ann Leong April 21, 2006 Acknowledgments. Hawaii Institute of Marine Biology (HIMB) acknowledges the support of Senator Daniel K. Inouye’s Office, the National Marine Sanctuary Program (NMSP), the Northwestern Hawaiian Islands Coral Reef Ecosystem Reserve (NWHICRER), State of Hawaii Department of Land and Natural Resources (DLNR) Division of Aquatic Resources, US Fish and Wildlife Service, NOAA Fisheries, and the numerous University of Hawaii partners involved in this project. Funding provided by NMSP MOA 2005-008/66832. Photos provided by NOAA NWHICRER and HIMB. Aerial photo of Moku o Lo‘e (Coconut Island) by Brent Daniel. Background The Hawai‘i Institute of Marine Biology (School of Ocean and Earth Science and Technology, University of Hawai‘i at Mānoa) signed a memorandum of agreement with National Marine Sanctuary Program (NOS, NOAA) on March 28, 2005, to assist the Northwestern Hawaiian Islands Coral Reef Ecosystem Reserve (NWHICRER) with scientific research required for the development of a science-based ecosystem management plan. With this overriding objective, a scope of work was developed to: 1. Understand the population structures of bottomfish, lobsters, reef fish, endemic coral species, and adult predator species in the NWHI. -
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. -
Centropyge, Pomacanthidae
Galaxea, Journal of Coral Reef Studies 22: 31-36(2020) Note Filling an empty role: first report of cleaning by pygmy angelfishes (Centropyge, Pomacanthidae) Pauline NARVAEZ*1, 2, 3 and Renato A. MORAIS1, 3 1 ARC Centre of Excellence for Coral Reef Studies, 1 James Cook Drive, Townsville, Queensland 4810, Australia 2 Centre for Sustainable Tropical Fisheries and Aquaculture, James Cook University, 1 James Cook Drive, Townsville, Queensland 4810, Australia 3 College of Science and Engineering, James Cook University, 1 James Cook Drive, Townsville, Queensland 4810, Aus tralia * Corresponding author: Pauline Narvaez Email: [email protected] Communicated by Frederic Sinniger (Associate EditorinChief) Abstract Cleaner fishes remove ectoparasites, mucus and search of ectoparasites, mucus, and dead or diseased dead tissues from other ‘client’ organisms. These mutu tissue (Côté 2000; Côté and Soares 2011). Cleaners have alistic interactions provide benefits for the ‘clients’ and, been classified as either dedicated or facultative, depend on a larger scale, maintain healthy reef ecosystems. Here, ing on their degree of reliance on cleaning interactions for we report two species of angelfishes, Centropyge bicolor accessing food (Vaughan et al. 2017). While dedicated and C. tibicen, acting as cleaners of the blue tang cleaners rely almost exclusively on cleaning, facultative Paracanthurus hepatus in an aquarium. This observation ones also exploit other food sources. In total, 208 fish and is the first time that pygmy angelfishes are recorded 51 shrimp species have been reported as either dedicated cleaning in any en vironment. This novel cleaning ob or facultative cleaners (Vaughan et al. 2017). -
2.02 Rajasuriya 2008
ARJAN RAJASURIYA National Aquatic Resources Research and Development Agency, Crow Island, Colombo 15, Sri Lanka [email protected]; [email protected] fringing and patch reefs (Swan, 1983; Rajasuriya et al., 1995; Rajasuriya & White, 1995). Fringing coral reef Selected coral reefs were monitored in the northern, areas occur in a narrow band along the coast except in western and southern coastal waters of Sri Lanka to the southeast and northeast of the island where sand assess their current status and to understand the movement inhibits their formation. The shallow recovery processes after the 1998 coral bleaching event continental shelf of Gulf of Mannar contains extensive and the 2004 tsunami. The highest rate of recovery coral patch reefs from the Bar Reef to Mannar Island was observed at the Bar Reef Marine Sanctuary where (Rajasuriya, 1991; Rajasuriya, et al. 1998a; Rajasuriya rapid growth of Acropora cytherea and Pocillopora & Premaratne, 2000). In addition to these coral reefs, damicornis has contributed to reef recovery. which are limited to a depth of about 10m, there are Pocillopora damicornis has shown a high level of offshore coral patches in the west and east of the recruitment and growth on most reef habitats island at varying distances (15 -20 km) from the including reefs in the south. An increase in the growth coastline at an average depth of 20m (Rajasuriya, of the calcareous alga Halimeda and high levels of 2005). Sandstone and limestone reefs occur as sedimentation has negatively affected some fringing discontinuous bands parallel to the shore from inshore reefs especially in the south. Reef surveys carried out areas to the edge of the continental shelf (Swan, 1983; for the first time in the northern coastal waters around Rajasuriya et al., 1995). -
Coral Health and Disease in the Pacific: Vision for Action
IV. STATE OF KNOWLEDGE IN THE PACIFIC—WHAT DO WE KNOW AND WHAT HAVE WE LEARNED? OVERVIEW OF ISSUES UNIQUE TO THE PACIFIC: BIOLOGICAL & SOCIAL PERSPECTIVES Michael J. Gawel Guam EPA 120 Bengbing St. Y-Papao Dededo, GU 96929 [email protected] Pacific Islands The term “Pacific Islands” in the context of this paper arbitrarily refers to those tropical islands of the central and western Pacific Ocean which support shallow hermatypic coral reefs, but excluding the Hawaiian Archipelago, which is covered in other papers. The tropical Pacific Island nations and territories all support coral reefs and, no doubt, harbor coral diseases, although these have not been scientifically documented in many of the islands. In fact, as part of the U.S. National Action Plan to Conserve Coral Reefs, surveys in 2002 and 2004 of coral reef academic scientists, resource managers, government agencies and NGOs recorded that in the U.S. Pacific islands they perceived “no threat” from coral disease, although American Samoa registered an increase to perception of “moderate threat” in the 2004 survey (Waddell, 2005). This lack of concern partially reflects a lack of information on the status of diseases in many islands. Wilkinson (2004, p. 405) notes that in American Samoa and Micronesia “Coral bleaching and disease were either rare or undocumented in 1994, but are now clearly evident and considered a serious threat to many reefs in the region.” The Pacific island coral reefs range from veneers on newly emergent volcanic islands, to platform-like fringing reefs, to barrier reefs with lagoons, to atolls, and include non- emergent isolated banks. -
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 ................................................................................................... -
Reef Fishes of the Bird's Head Peninsula, West
Check List 5(3): 587–628, 2009. ISSN: 1809-127X LISTS OF SPECIES Reef fishes of the Bird’s Head Peninsula, West Papua, Indonesia Gerald R. Allen 1 Mark V. Erdmann 2 1 Department of Aquatic Zoology, Western Australian Museum. Locked Bag 49, Welshpool DC, Perth, Western Australia 6986. E-mail: [email protected] 2 Conservation International Indonesia Marine Program. Jl. Dr. Muwardi No. 17, Renon, Denpasar 80235 Indonesia. Abstract A checklist of shallow (to 60 m depth) reef fishes is provided for the Bird’s Head Peninsula region of West Papua, Indonesia. The area, which occupies the extreme western end of New Guinea, contains the world’s most diverse assemblage of coral reef fishes. The current checklist, which includes both historical records and recent survey results, includes 1,511 species in 451 genera and 111 families. Respective species totals for the three main coral reef areas – Raja Ampat Islands, Fakfak-Kaimana coast, and Cenderawasih Bay – are 1320, 995, and 877. In addition to its extraordinary species diversity, the region exhibits a remarkable level of endemism considering its relatively small area. A total of 26 species in 14 families are currently considered to be confined to the region. Introduction and finally a complex geologic past highlighted The region consisting of eastern Indonesia, East by shifting island arcs, oceanic plate collisions, Timor, Sabah, Philippines, Papua New Guinea, and widely fluctuating sea levels (Polhemus and the Solomon Islands is the global centre of 2007). reef fish diversity (Allen 2008). Approximately 2,460 species or 60 percent of the entire reef fish The Bird’s Head Peninsula and surrounding fauna of the Indo-West Pacific inhabits this waters has attracted the attention of naturalists and region, which is commonly referred to as the scientists ever since it was first visited by Coral Triangle (CT).