Coral Demographic Training
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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. -
Comprehensive Phylogenomic Analyses Resolve Cnidarian Relationships and the Origins of Key Organismal Traits
Comprehensive phylogenomic analyses resolve cnidarian relationships and the origins of key organismal traits Ehsan Kayal1,2, Bastian Bentlage1,3, M. Sabrina Pankey5, Aki H. Ohdera4, Monica Medina4, David C. Plachetzki5*, Allen G. Collins1,6, Joseph F. Ryan7,8* Authors Institutions: 1. Department of Invertebrate Zoology, National Museum of Natural History, Smithsonian Institution 2. UPMC, CNRS, FR2424, ABiMS, Station Biologique, 29680 Roscoff, France 3. Marine Laboratory, university of Guam, UOG Station, Mangilao, GU 96923, USA 4. Department of Biology, Pennsylvania State University, University Park, PA, USA 5. Department of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH, USA 6. National Systematics Laboratory, NOAA Fisheries, National Museum of Natural History, Smithsonian Institution 7. Whitney Laboratory for Marine Bioscience, University of Florida, St Augustine, FL, USA 8. Department of Biology, University of Florida, Gainesville, FL, USA PeerJ Preprints | https://doi.org/10.7287/peerj.preprints.3172v1 | CC BY 4.0 Open Access | rec: 21 Aug 2017, publ: 21 Aug 20171 Abstract Background: The phylogeny of Cnidaria has been a source of debate for decades, during which nearly all-possible relationships among the major lineages have been proposed. The ecological success of Cnidaria is predicated on several fascinating organismal innovations including symbiosis, colonial body plans and elaborate life histories, however, understanding the origins and subsequent diversification of these traits remains difficult due to persistent uncertainty surrounding the evolutionary relationships within Cnidaria. While recent phylogenomic studies have advanced our knowledge of the cnidarian tree of life, no analysis to date has included genome scale data for each major cnidarian lineage. Results: Here we describe a well-supported hypothesis for cnidarian phylogeny based on phylogenomic analyses of new and existing genome scale data that includes representatives of all cnidarian classes. -
Patterns of Septal Biomineralization in Scleractinia Compared with Their 28S Rrna Phylogeny
PBlackwell Publishingatterns Ltd. of septal biomineralization in Scleractinia compared with their 28S rRNA phylogeny: a dual approach for a new taxonomic framework JEAN-PIERRE CUIF, GUILLAUME LECOINTRE, CHRISTINE PERRIN, ANNIE TILLIER & SIMON TILLIER Accepted: 2 December 2002 Cuif, J.-P., Lecointre, G., Perrin, C., Tillier, A. & Tillier, S. (2003). Patterns of septal bio- mineralization in Scleractinia compared with their 28S rRNA phylogeny: a dual approach for a new taxonomic framework. — Zoologica Scripta, 32, 459–473. A molecular phylogeny of the Scleractinia is reconstructed from approximately 700 nucleo- tides of the 5′end of the 28S rDNA obtained from 40 species. A comparison of molecular phylogenic trees with biomineralization patterns of coral septa suggests that at least five clades are corroborated by both types of data. Agaricidae and Dendrophylliidae are found to be monophyletic, that is supported by microstructural data. Conversely, Faviidae and Caryophyl- liidae are found to be paraphyletic: Cladocora should be excluded from the faviids, whereas Eusmilia should be excluded from the caryophylliids. The conclusion is also supported by the positions, sizes and shapes of centres of calcification. The traditional Guyniidae are diphyletic, corroborating Stolarski’s hypothesis ‘A’. Some results from our most parsimonious trees are not strongly statistically supported but corroborated by other molecular studies and micro- structural observations. For example, in the scleractinian phylogenetic tree, there are several lines of evidence (including those from our data) to distinguish a Faviidae–Mussidae lineage and a Dendrophylliidae–Agaricidae–Poritidae–Siderastreidae lineage. From a methodological standpoint, our results suggest that co-ordinated studies creating links between biomineralization patterns and molecular phylogeny may provide an efficient working approach for a re- examination of scleractinian classification. -
The Genetic Identity of Dinoflagellate Symbionts in Caribbean Octocorals
Coral Reefs (2004) 23: 465-472 DOI 10.1007/S00338-004-0408-8 REPORT Tamar L. Goulet • Mary Alice CofFroth The genetic identity of dinoflagellate symbionts in Caribbean octocorals Received: 2 September 2002 / Accepted: 20 December 2003 / Published online: 29 July 2004 © Springer-Verlag 2004 Abstract Many cnidarians (e.g., corals, octocorals, sea Introduction anemones) maintain a symbiosis with dinoflagellates (zooxanthellae). Zooxanthellae are grouped into The cornerstone of the coral reef ecosystem is the sym- clades, with studies focusing on scleractinian corals. biosis between cnidarians (e.g., corals, octocorals, sea We characterized zooxanthellae in 35 species of Caribbean octocorals. Most Caribbean octocoral spe- anemones) and unicellular dinoñagellates commonly called zooxanthellae. Studies of zooxanthella symbioses cies (88.6%) hosted clade B zooxanthellae, 8.6% have previously been hampered by the difficulty of hosted clade C, and one species (2.9%) hosted clades B and C. Erythropodium caribaeorum harbored clade identifying the algae. Past techniques relied on culturing and/or identifying zooxanthellae based on their free- C and a unique RFLP pattern, which, when se- swimming form (Trench 1997), antigenic features quenced, fell within clade C. Five octocoral species (Kinzie and Chee 1982), and cell architecture (Blank displayed no zooxanthella cladal variation with depth. 1987), among others. These techniques were time-con- Nine of the ten octocoral species sampled throughout suming, required a great deal of expertise, and resulted the Caribbean exhibited no regional zooxanthella cla- in the differentiation of only a small number of zoo- dal differences. The exception, Briareum asbestinum, xanthella species. Molecular techniques amplifying had some colonies from the Dry Tortugas exhibiting zooxanthella DNA encoding for the small and large the E. -
Coral Injuries Caused by Spirobranchus Opercula with and Without Epibiotic Turf Algae at Curaçao
Marine Biology (2019) 166:60 https://doi.org/10.1007/s00227-019-3504-6 SHORT NOTE Coral injuries caused by Spirobranchus opercula with and without epibiotic turf algae at Curaçao Bert W. Hoeksema1,2 · Dagmar Wels1 · Roeland J. van der Schoot1 · Harry A. ten Hove1 Received: 11 January 2019 / Accepted: 26 March 2019 © The Author(s) 2019 Abstract Reef-dwelling Christmas tree worms (Spirobranchus spp.) are common coral associates. Their calcareous tubes are usually embedded in the coral skeleton and can be closed by an operculum. Tubes not overgrown by coral tissue either remain bare or become covered by algae. Despite their widespread distribution, high abundance and striking appearance, little is known about the impact of these worms on their hosts. We quantifed visible coral damage caused by Spirobranchus in Curaçao (Southern Caribbean) and found that 62.6% of worm opercula (n = 1323) caused abrasions and tissue loss in their hosts. Filamentous turf algae, known to be potentially harmful to corals, covered 76.9% of the opercula. Examination of the six most frequently inhabited host species showed a variation in the damage percentages, although this was independent of the presence of epibiotic algae on 78.4% of all opercula. Since injured corals are more susceptible to diseases, the overall nega- tive impact of Spirobranchus worms on their hosts may be more severe than previously assumed. Introduction and Nishihira 1996), even if the host becomes overgrown by sponges and octocorals, which in turn can act as replacement Coral-dwelling tubeworms of the genus Spirobranchus hosts (Hoeksema et al. 2015, 2016; García-Hernández and (Polychaeta: Serpulidae), known popularly as Christmas Hoeksema 2017). -
Volume 2. Animals
AC20 Doc. 8.5 Annex (English only/Seulement en anglais/Únicamente en inglés) REVIEW OF SIGNIFICANT TRADE ANALYSIS OF TRADE TRENDS WITH NOTES ON THE CONSERVATION STATUS OF SELECTED SPECIES Volume 2. Animals Prepared for the CITES Animals Committee, CITES Secretariat by the United Nations Environment Programme World Conservation Monitoring Centre JANUARY 2004 AC20 Doc. 8.5 – p. 3 Prepared and produced by: UNEP World Conservation Monitoring Centre, Cambridge, UK UNEP WORLD CONSERVATION MONITORING CENTRE (UNEP-WCMC) www.unep-wcmc.org The UNEP World Conservation Monitoring Centre is the biodiversity assessment and policy implementation arm of the United Nations Environment Programme, the world’s foremost intergovernmental environmental organisation. UNEP-WCMC aims to help decision-makers recognise the value of biodiversity to people everywhere, and to apply this knowledge to all that they do. The Centre’s challenge is to transform complex data into policy-relevant information, to build tools and systems for analysis and integration, and to support the needs of nations and the international community as they engage in joint programmes of action. UNEP-WCMC provides objective, scientifically rigorous products and services that include ecosystem assessments, support for implementation of environmental agreements, regional and global biodiversity information, research on threats and impacts, and development of future scenarios for the living world. Prepared for: The CITES Secretariat, Geneva A contribution to UNEP - The United Nations Environment Programme Printed by: UNEP World Conservation Monitoring Centre 219 Huntingdon Road, Cambridge CB3 0DL, UK © Copyright: UNEP World Conservation Monitoring Centre/CITES Secretariat The contents of this report do not necessarily reflect the views or policies of UNEP or contributory organisations. -
New and Old Scleractinian Corals from Jamaica
CORAL REEF PROJECT-PAPERS IN MEMORY OF DR. THOMAS F. GOREAU. 2. NEW AND OLD SCLERACTINIAN CORALS FROM JAMAICA JOHN W. WELLS Department of Geological Sciences, Cornell University, Ithaca, New York ABSTRACT The underwater studies of Jamaican reefs carried out during the past 17 years by the late T. F. Goreau and his colleagues have turned up a number of new species of scleractinian corals and disclosed the common occurrence at depth of several species previously thought to be rare. The new forms include one species of Madracis, one of Agaricia, three of Mycetophyllia, one of Gardineria, and new forms of Eusmilia fastigiata and Agaricia fragilis. Earlier named but poorly known species discussed and figured are: Agaricia undata (Ellis & Solander), Agaricia lamarcki Milne Edwards & Haime, A. tenuitolia (Dana), He/ioseris cucul/ata (Ellis & Solander), Colpophyllia breviseria/is Milne Edwards & Haime, Mycetophyllia danaana Milne Edwards & Haime, and Di- chacaenia stellaris Milne Edwards & Haime. INTRODUCTION During the course of an extended study of the corals and coral reefs of Jamaica by the late T. F. Goreau and his associates at the Discovery Bay Marine Laboratory, the distribution of the hermatypic and ahermatypic scleractinian corals has been a special concern, for while the occurrence and zonation of corals on the shallower parts of West Indian reefs is fairly well known, the situation at depth had been otherwise until the use of SCUBA equipment made possible detailed examination and collection to depths of as much as 100 meters. A preliminary list of the scleractinian corals of the Jamaican reefs was published by Gareau & Wells in 1967, in which the presence of several new species was indicated. -
UC Merced UC Merced Electronic Theses and Dissertations
UC Merced UC Merced Electronic Theses and Dissertations Title Deep Amplicon Sequencing Quantitatively Detected Mixed Community Assemblages of Symbiodinium in Orbicella faveolata and Orbicella franksi Permalink https://escholarship.org/uc/item/31n4975j Author Green, Elizabeth Publication Date 2014 Peer reviewed|Thesis/dissertation eScholarship.org Powered by the California Digital Library University of California UNIVERSITY OF CALIFORNIA, MERCED Deep Amplicon Sequencing Quantitatively Detected Mixed Community Assemblages of Symbiodinium in Orbicella faveolata and Orbicella franksi THESIS submitted in partial satisfaction of the requirements for the degree of MASTER OF SCIENCE in Quantitative and Systems Biology by Elizabeth A. Green Committee in charge: David Ardell, chair Miriam Barlow Mónica Medina Michele Weber 2014 © Elizabeth A. Green, 2014 All rights reserved The thesis of Elizabeth A. Green is approved, and it is acceptable in quality and form for publication on microfilm and electronically: Miriam Barlow Mónica Medina Michele Weber David Ardell Chair University of California, Merced 2014 iii Dedication This thesis is dedicated to my loving and supportive husband, Colten Green. iv Table of Contents Page SIGNATURE PAGE ……………………….…………………………………… iii LIST OF FIGURES ……………………………………………………………... vi LIST OF TABLES ………………………………………………………………. vii ACKNOWLEDGEMENTS ……………………………………………………… viii ABSTRACT ……………………………………………………………………… ix INTRODUCTION ………………………………………………………………… 1 METHODS ………………………………………………………………………… 6 RESULTS …………………………………………………………………………. -
Marine Ecology Progress Series 506:129
Vol. 506: 129–144, 2014 MARINE ECOLOGY PROGRESS SERIES Published June 23 doi: 10.3354/meps10808 Mar Ecol Prog Ser FREEREE ACCESSCCESS Long-term changes in Symbiodinium communities in Orbicella annularis in St. John, US Virgin Islands Peter J. Edmunds1,*, Xavier Pochon2,3, Don R. Levitan4, Denise M. Yost2, Mahdi Belcaid2, Hollie M. Putnam2, Ruth D. Gates2 1Department of Biology, California State University, 18111 Nordhoff Street, Northridge, CA 91330-8303, USA 2Hawaii Institute of Marine Biology, University of Hawaii, PO Box 1346, Kaneohe, HI 96744, USA 3Environmental Technologies, Cawthron Institute, 98 Halifax Street East, Private Bag 2, Nelson 7042, New Zealand 4Department of Biological Science, Florida State University, Tallahassee, FL 32306-4295, USA ABSTRACT: Efforts to monitor coral reefs rarely combine ecological and genetic tools to provide insight into the processes driving patterns of change. We focused on a coral reef at 14 m depth in St. John, US Virgin Islands, and used both sets of tools to examine 12 colonies of Orbicella (for- merly Montastraea) annularis in 2 photoquadrats that were monitored for 16 yr and sampled genetically at the start and end of the study. Coral cover and colony growth were assessed annu- ally, microsatellites were used to genetically identify coral hosts in 2010, and their Symbiodinium were genotyped using chloroplastic 23S (cloning) and nuclear ITS2 (cloning and pyrosequencing) in 1994 and 2010. Coral cover declined from 40 to 28% between 1994 and 2010, and 3 of the 12 sampled colonies increased in size, while 9 decreased in size. The relative abundance of Symbio- dinium clades varied among corals over time, and patterns of change differed between photo- quadrats but not among host genotypes. -
Volume III of This Document)
4.1.3 Coastal Migratory Pelagics Description and Distribution (from CMP Am 15) The coastal migratory pelagics management unit includes cero (Scomberomous regalis), cobia (Rachycentron canadum), king mackerel (Scomberomous cavalla), Spanish mackerel (Scomberomorus maculatus) and little tunny (Euthynnus alleterattus). The mackerels and tuna in this management unit are often referred to as ―scombrids.‖ The family Scombridae includes tunas, mackerels and bonitos. They are among the most important commercial and sport fishes. The habitat of adults in the coastal pelagic management unit is the coastal waters out to the edge of the continental shelf in the Atlantic Ocean. Within the area, the occurrence of coastal migratory pelagic species is governed by temperature and salinity. All species are seldom found in water temperatures less than 20°C. Salinity preference varies, but these species generally prefer high salinity. The scombrids prefer high salinities, but less than 36 ppt. Salinity preference of little tunny and cobia is not well defined. The larval habitat of all species in the coastal pelagic management unit is the water column. Within the spawning area, eggs and larvae are concentrated in the surface waters. (from PH draft Mackerel Am. 18) King Mackerel King mackerel is a marine pelagic species that is found throughout the Gulf of Mexico and Caribbean Sea and along the western Atlantic from the Gulf of Maine to Brazil and from the shore to 200 meter depths. Adults are known to spawn in areas of low turbidity, with salinity and temperatures of approximately 30 ppt and 27°C, respectively. There are major spawning areas off Louisiana and Texas in the Gulf (McEachran and Finucane 1979); and off the Carolinas, Cape Canaveral, and Miami in the western Atlantic (Wollam 1970; Schekter 1971; Mayo 1973). -
Bacterial Profiling of White Plague Disease Across Corals and Oceans
Molecular Ecology (2014) 23, 965–974 doi: 10.1111/mec.12638 Bacterial profiling of White Plague Disease across corals and oceans indicates a conserved and distinct disease microbiome CORNELIA RODER,* CHATCHANIT ARIF,* CAMILLE DANIELS,* ERNESTO WEIL† and CHRISTIAN R. VOOLSTRA* *Red Sea Research Center, King Abdullah University of Science and Technology, 23955 Thuwal, Saudi Arabia, †Department of Marine Sciences, University of Puerto Rico, PO BOX 9000, Mayaguez, Puerto Rico 00680, USA Abstract Coral diseases are characterized by microbial community shifts in coral mucus and tissue, but causes and consequences of these changes are vaguely understood due to the complexity and dynamics of coral-associated bacteria. We used 16S rRNA gene microarrays to assay differences in bacterial assemblages of healthy and diseased colo- nies displaying White Plague Disease (WPD) signs from two closely related Caribbean coral species, Orbicella faveolata and Orbicella franksi. Analysis of differentially abun- dant operational taxonomic units (OTUs) revealed strong differences between healthy and diseased specimens, but not between coral species. A subsequent comparison to data from two Indo-Pacific coral species (Pavona duerdeni and Porites lutea) revealed distinct microbial community patterns associated with ocean basin, coral species and health state. Coral species were clearly separated by site, but also, the relatedness of the underlying bacterial community structures resembled the phylogenetic relationship of the coral hosts. In diseased samples, bacterial richness increased and putatively opportunistic bacteria were consistently more abundant highlighting the role of oppor- tunistic conditions in structuring microbial community patterns during disease. Our comparative analysis shows that it is possible to derive conserved bacterial footprints of diseased coral holobionts that might help in identifying key bacterial species related to the underlying etiopathology. -
Coral-Associated Bacteria Demonstrate Phylosymbiosis and Cophylogeny
ARTICLE DOI: 10.1038/s41467-018-07275-x OPEN Coral-associated bacteria demonstrate phylosymbiosis and cophylogeny F. Joseph Pollock1, Ryan McMinds 2, Styles Smith1, David G. Bourne3,4, Bette L. Willis3,5, Mónica Medina 1,6, Rebecca Vega Thurber2 & Jesse R. Zaneveld7 Scleractinian corals’ microbial symbionts influence host health, yet how coral microbiomes assembled over evolution is not well understood. We survey bacterial and archaeal 1234567890():,; communities in phylogenetically diverse Australian corals representing more than 425 million years of diversification. We show that coral microbiomes are anatomically compartmenta- lized in both modern microbial ecology and evolutionary assembly. Coral mucus, tissue, and skeleton microbiomes differ in microbial community composition, richness, and response to host vs. environmental drivers. We also find evidence of coral-microbe phylosymbiosis, in which coral microbiome composition and richness reflect coral phylogeny. Surprisingly, the coral skeleton represents the most biodiverse coral microbiome, and also shows the stron- gest evidence of phylosymbiosis. Interactions between bacterial and coral phylogeny sig- nificantly influence the abundance of four groups of bacteria–including Endozoicomonas-like bacteria, which divide into host-generalist and host-specific subclades. Together these results trace microbial symbiosis across anatomy during the evolution of a basal animal lineage. 1 Department of Biology, Pennsylvania State University, 208 Mueller Lab, University Park, State College, PA 16802, USA. 2 Department of Microbiology, Oregon State University, 226 Nash Hall, Corvallis, OR 97331, USA. 3 College of Science and Engineering, James Cook University, Townsville, QLD 4811, Australia. 4 Australian Institute of Marine Science, Townsville, QLD 4810, Australia. 5 ARC Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, QLD 4811, Australia.