SESSILE INVERTEBRATES Sessile Invertebrates Are Those Animals Without Backbones That Are Attached to the Reef
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MARINE FAUNA and FLORA of BERMUDA a Systematic Guide to the Identification of Marine Organisms
MARINE FAUNA AND FLORA OF BERMUDA A Systematic Guide to the Identification of Marine Organisms Edited by WOLFGANG STERRER Bermuda Biological Station St. George's, Bermuda in cooperation with Christiane Schoepfer-Sterrer and 63 text contributors A Wiley-Interscience Publication JOHN WILEY & SONS New York Chichester Brisbane Toronto Singapore ANTHOZOA 159 sucker) on the exumbrella. Color vari many Actiniaria and Ceriantharia can able, mostly greenish gray-blue, the move if exposed to unfavorable condi greenish color due to zooxanthellae tions. Actiniaria can creep along on their embedded in the mesoglea. Polyp pedal discs at 8-10 cm/hr, pull themselves slender; strobilation of the monodisc by their tentacles, move by peristalsis type. Medusae are found, upside through loose sediment, float in currents, down and usually in large congrega and even swim by coordinated tentacular tions, on the muddy bottoms of in motion. shore bays and ponds. Both subclasses are represented in Ber W. STERRER muda. Because the orders are so diverse morphologically, they are often discussed separately. In some classifications the an Class Anthozoa (Corals, anemones) thozoan orders are grouped into 3 (not the 2 considered here) subclasses, splitting off CHARACTERISTICS: Exclusively polypoid, sol the Ceriantharia and Antipatharia into a itary or colonial eNIDARIA. Oral end ex separate subclass, the Ceriantipatharia. panded into oral disc which bears the mouth and Corallimorpharia are sometimes consid one or more rings of hollow tentacles. ered a suborder of Scleractinia. Approxi Stomodeum well developed, often with 1 or 2 mately 6,500 species of Anthozoa are siphonoglyphs. Gastrovascular cavity compart known. Of 93 species reported from Ber mentalized by radially arranged mesenteries. -
(Symbiodinium) in Scleractinian Corals from Tropical Reefs in Southern Hainan
Journal of Systematics and Evolution 49 (6): 598–605 (2011) doi: 10.1111/j.1759-6831.2011.00161.x Research Article Low genetic diversity of symbiotic dinoflagellates (Symbiodinium) in scleractinian corals from tropical reefs in southern Hainan Island, China 1,2Guo-Wei ZHOU 1,2Hui HUANG∗ 1(Key Laboratory of Marine Bio-resources Sustainable Utilization, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China) 2(Tropical Marine Biological Research Station in Hainan, Chinese Academy of Sciences, Sanya 572000, China) Abstract Endosymbiotic dinoflagellates in the genus Symbiodinium are among the most abundant and important group of photosynthetic protists found in coral reef ecosystems. In order to further characterize this diversity and compare with other regions of the Pacific, samples from 44 species of scleractinian corals representing 20 genera and 9 families, were collected from tropical reefs in southern Hainan Island, China. Denaturing gradient gel electrophoresis fingerprinting of the ribosomal internal transcribed spacer 2 identified 11 genetically distinct Symbiodinium types that have been reported previously. The majority of reef-building coral species (88.6%) harbored only one subcladal type of symbiont, dominated by host-generalist C1 and C3, and was influenced little by the host’s apparent mode of symbiont acquisition. Some species harbored more than one clade of Symbiodinium (clades C, D) concurrently. Although geographically isolated from the rest of the Pacific, the symbiont diversity in southern Hainan Island was relatively low and similar to both the Great Barrier Reef and Hawaii symbiont assemblages (dominated by clade C Symbiodinium). These results indicate that a specialist symbiont is not a prerequisite for existence in remote and isolated areas, but additional work in other geographic regions is necessary to test this idea. -
Chromera Velia Is Endosymbiotic in Larvae of the Reef Corals Acropora
Protist, Vol. 164, 237–244, March 2013 http://www.elsevier.de/protis Published online date 12 October 2012 ORIGINAL PAPER Chromera velia is Endosymbiotic in Larvae of the Reef Corals Acropora digitifera and A. tenuis a,b,1 b c,d e Vivian R. Cumbo , Andrew H. Baird , Robert B. Moore , Andrew P. Negri , c f e c Brett A. Neilan , Anya Salih , Madeleine J.H. van Oppen , Yan Wang , and c Christopher P. Marquis a School of Marine and Tropical Biology, James Cook University, Townsville, Queensland, 4811, Australia b ARC Centre of Excellence for Reef Studies, James Cook University, Townsville, Queensland, 4811, Australia c School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia d School of Biological Sciences, Flinders University, GPO Box 2100, Adelaide SA 5001, Australia e Australian Institute of Marine Science PMB 3, Townsville, Queensland, 4810, Australia f Confocal Bio-Imaging Facility, School of Science and Health, University of Western Sydney, NSW 2006, Australia Submitted May 8, 2012; Accepted August 30, 2012 Monitoring Editor: Bland J. Finlay Scleractinian corals occur in symbiosis with a range of organisms including the dinoflagellate alga, Symbiodinium, an association that is mutualistic. However, not all symbionts benefit the host. In par- ticular, many organisms within the microbial mucus layer that covers the coral epithelium can cause disease and death. Other organisms in symbiosis with corals include the recently described Chromera velia, a photosynthetic relative of the apicomplexan parasites that shares a common ancestor with Symbiodinium. To explore the nature of the association between C. velia and corals we first isolated C. -
Taxonomy and Phylogenetic Relationships of the Coral Genera Australomussa and Parascolymia (Scleractinia, Lobophylliidae)
Contributions to Zoology, 83 (3) 195-215 (2014) Taxonomy and phylogenetic relationships of the coral genera Australomussa and Parascolymia (Scleractinia, Lobophylliidae) Roberto Arrigoni1, 7, Zoe T. Richards2, Chaolun Allen Chen3, 4, Andrew H. Baird5, Francesca Benzoni1, 6 1 Dept. of Biotechnology and Biosciences, University of Milano-Bicocca, 20126, Milan, Italy 2 Aquatic Zoology, Western Australian Museum, 49 Kew Street, Welshpool, WA 6106, Australia 3Biodiversity Research Centre, Academia Sinica, Nangang, Taipei 115, Taiwan 4 Institute of Oceanography, National Taiwan University, Taipei 106, Taiwan 5 ARC Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, QLD 4811, Australia 6 Institut de Recherche pour le Développement, UMR227 Coreus2, 101 Promenade Roger Laroque, BP A5, 98848 Noumea Cedex, New Caledonia 7 E-mail: [email protected] Key words: COI, evolution, histone H3, Lobophyllia, Pacific Ocean, rDNA, Symphyllia, systematics, taxonomic revision Abstract Molecular phylogeny of P. rowleyensis and P. vitiensis . 209 Utility of the examined molecular markers ....................... 209 Novel micromorphological characters in combination with mo- Acknowledgements ...................................................................... 210 lecular studies have led to an extensive revision of the taxonomy References ...................................................................................... 210 and systematics of scleractinian corals. In the present work, we Appendix ....................................................................................... -
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. -
Molecular Identification of Symbiotic Dinoflagellates in Pacific Corals in the Genus Pocillopora Hélène Magalon, Jean-François Flot, Emmanuelle Baudry
Molecular identification of symbiotic dinoflagellates in Pacific corals in the genus Pocillopora Hélène Magalon, Jean-François Flot, Emmanuelle Baudry To cite this version: Hélène Magalon, Jean-François Flot, Emmanuelle Baudry. Molecular identification of symbiotic di- noflagellates in Pacific corals in the genus Pocillopora. Coral Reefs, Springer Verlag, 2007, 26(3), pp.551-558. hal-00941744 HAL Id: hal-00941744 https://hal.archives-ouvertes.fr/hal-00941744 Submitted on 6 May 2016 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. Molecular identiWcation of symbiotic dinoXagellates in PaciWc corals in the genus Pocillopora H. Magalon · J.-F. Flot · E. Baudry Abstract This study focused on the association between Introduction corals of the genus Pocillopora, a major constituent of PaciWc reefs, and their zooxanthellae. Samples of Most tropical corals live in symbiosis with photosynthetic P. meandrina, P. verrucosa, P. damicornis, P. eydouxi, algae, the zooxanthellae (reviewed in Trench 1993). Most P. ligulata and P. molokensis were collected from French zooxanthellae belong to the genus Symbiodinium and 11 Polynesia, Tonga, Okinawa and Hawaii. Symbiodinium species have now been deWned based on morphological, diversity was explored by looking at the 28S and ITS1 physiological and molecular criteria (reviewed in Baker regions of the ribosomal DNA. -
Final Corals Supplemental Information Report
Supplemental Information Report on Status Review Report And Draft Management Report For 82 Coral Candidate Species November 2012 Southeast and Pacific Islands Regional Offices National Marine Fisheries Service National Oceanic and Atmospheric Administration Department of Commerce Table of Contents INTRODUCTION ............................................................................................................................................. 1 Background ............................................................................................................................................... 1 Methods .................................................................................................................................................... 1 Purpose ..................................................................................................................................................... 2 MISCELLANEOUS COMMENTS RECEIVED ...................................................................................................... 3 SRR EXECUTIVE SUMMARY ........................................................................................................................... 4 1. Introduction ........................................................................................................................................... 4 2. General Background on Corals and Coral Reefs .................................................................................... 4 2.1 Taxonomy & Distribution ............................................................................................................. -
The Earliest Diverging Extant Scleractinian Corals Recovered by Mitochondrial Genomes Isabela G
www.nature.com/scientificreports OPEN The earliest diverging extant scleractinian corals recovered by mitochondrial genomes Isabela G. L. Seiblitz1,2*, Kátia C. C. Capel2, Jarosław Stolarski3, Zheng Bin Randolph Quek4, Danwei Huang4,5 & Marcelo V. Kitahara1,2 Evolutionary reconstructions of scleractinian corals have a discrepant proportion of zooxanthellate reef-building species in relation to their azooxanthellate deep-sea counterparts. In particular, the earliest diverging “Basal” lineage remains poorly studied compared to “Robust” and “Complex” corals. The lack of data from corals other than reef-building species impairs a broader understanding of scleractinian evolution. Here, based on complete mitogenomes, the early onset of azooxanthellate corals is explored focusing on one of the most morphologically distinct families, Micrabaciidae. Sequenced on both Illumina and Sanger platforms, mitogenomes of four micrabaciids range from 19,048 to 19,542 bp and have gene content and order similar to the majority of scleractinians. Phylogenies containing all mitochondrial genes confrm the monophyly of Micrabaciidae as a sister group to the rest of Scleractinia. This topology not only corroborates the hypothesis of a solitary and azooxanthellate ancestor for the order, but also agrees with the unique skeletal microstructure previously found in the family. Moreover, the early-diverging position of micrabaciids followed by gardineriids reinforces the previously observed macromorphological similarities between micrabaciids and Corallimorpharia as -
Oborník M.& Lukeš, J. (2013) Cell Biology of Chromerids: Autotrophic
CHAPTER EIGHT Cell Biology of Chromerids: Autotrophic Relatives to Apicomplexan Parasites Miroslav Oborník*,†,{,1, Julius Lukeš*,† *Biology Centre, Institute of Parasitology, Academy of Sciences of the Czech Republic, Cˇ eske´ Budeˇjovice, Czech Republic †Faculty of Science, University of South Bohemia, Cˇ eske´ Budeˇjovice, Czech Republic { Institute of Microbiology, Academy of Sciences of the Czech Republic, Trˇebonˇ, Czech Republic 1Corresponding author: e-mail address: [email protected] Contents 1. Introduction 334 2. Chromerida: A New Group of Algae Isolated from Australian Corals 337 2.1 C. velia: A new alga from Sydney Harbor 338 2.2 V. brassicaformis: An alga from the Great Barrier Reef 343 3. Life Cycle 346 4. Evolution of Exosymbiont 348 5. Evolution of Chromerid Organelles 350 5.1 Evolution of chromerid plastids 350 5.2 Reduced mitochondrial genomes of chromerids 354 5.3 Chromerosome: C. velia as a possible mixotroph 354 6. Metabolism of Chromerids 355 6.1 Unique pathway for tetrapyrrole biosynthesis 355 6.2 Other metabolic features of C. velia 359 7. Chromerids as Possible Symbionts of Corals 361 8. Conclusions 361 Acknowledgments 362 References 362 Abstract Chromerida are algae possessing a complex plastid surrounded by four membranes. Although isolated originally from stony corals in Australia, they seem to be globally dis- tributed. According to their molecular phylogeny, morphology, ultrastructure, structure of organellar genomes, and noncanonical pathway for tetrapyrrole synthesis, these algae are thought to be the closest known phototrophic relatives to apicomplexan par- asites. Here, we summarize the current knowledge of cell biology and evolution of this novel group of algae, which contains only two formally described species, but is appar- ently highly diverse and virtually ubiquitous in marine environments. -
Sedimentary Nitrogen Uptake & Assimilation in the Temperate
Sedimentary Nitrogen Uptake & Assimilation in the Temperate Zooxanthellate Anemone Anthopleura aureoradiata Sedimentary Nitrogen Uptake & Assimilation in the Temperate Zooxanthellate Anemone Anthopleura aureoradiata _______________________________________________ by Shyam Ravi Morar A thesis submitted to the Victoria University of Wellington in partial fulfilment of the requirements for the degree of Masters of Science in Marine Biology Victoria University of Wellington School of Biological Sciences 2008 ACKNOWLEDGEMENTS I would like to express my gratitude to Dr Joanne Davy & Milena Palka, for providing me with field dissolved nutrient data; Dr Geoff Chambers for allowing me to utilise the School of Biological Sciences radioactive facilities; Dr Matt Mills for his expertise and willingness to answer questions regarding his work; Dr Ken Ryan, for equipment and experimental advice; Dr Sarah Bury and the staff at the DeltaPlus Mass Spectrometry lab at National Institute of Water and Atmospheric Research, Wellington for sample analyses, but more importantly for taking the time to help someone new to isotopes; My good friends, Dmitri and Glenn for giving up their holiday time to help with preliminary fieldwork; “Professor” Christopher Gibbons for his help and friendship throughout the grad-school ordeal. A big thanks also to technician Joanne Long for prompt provisions with equipment and helpful advice whenever needed. An additional thanks to Drs Clayton Cook and Ken Ryan for grading the initial copy of this thesis and providing useful comments for preparation of this final version, as well as a subsequent manuscript. To the greatest supervisor on this planet Dr Simon Davy, which without, none of this would have been possible – thank you so very much for giving me the opportunity to be one of your students. -
The Reproductive Biology of the Scleractinian Coral Plesiastrea Versipora in Sydney Harbour, Australia
Vol. 1: 25–33, 2014 SEXUALITY AND EARLY DEVELOPMENT IN AQUATIC ORGANISMS Published online February 6 doi: 10.3354/sedao00004 Sex Early Dev Aquat Org OPEN ACCESS The reproductive biology of the scleractinian coral Plesiastrea versipora in Sydney Harbour, Australia Alisha Madsen1, Joshua S. Madin1, Chung-Hong Tan2, Andrew H. Baird2,* 1Department of Biological Sciences, Macquarie University, Sydney, New South Wales 2109, Australia 2ARC Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, Queensland 4811, Australia ABSTRACT: The scleractinian coral Plesiastrea versipora occurs throughout most of the Indo- Pacific; however, the species is only abundant in temperate regions, including Sydney Harbour, in New South Wales, Australia, where it can be the dominant sessile organism over small spatial scales. Population genetics indicates that the Sydney Harbour population is highly isolated, sug- gesting long-term persistence will depend upon on the local production of recruits. To determine the potential role of sexual reproduction in population persistence, we examined a number of fea- tures of the reproductive biology of P. versipora for the first time, including the sexual system, the length of the gametogenetic cycles and size-specific fecundity. P. versipora was gonochoric, sup- porting recent molecular work removing the species from the Family Merulinidae, in which the species are exclusively hermaphroditic. The oogenic cycle was between 13 and 14 mo and the spermatogenetic cycle between 7 and 8 mo, with broadcast spawning inferred to occur in either January or February. Colony sex was strongly influenced by colony size: the probability of being male increased with colony area. The longer oogenic cycle suggests that females are investing energy in reproduction rather than growth, and consequently, males are on average larger for a given age. -
CNIDARIA Corals, Medusae, Hydroids, Myxozoans
FOUR Phylum CNIDARIA corals, medusae, hydroids, myxozoans STEPHEN D. CAIRNS, LISA-ANN GERSHWIN, FRED J. BROOK, PHILIP PUGH, ELLIOT W. Dawson, OscaR OcaÑA V., WILLEM VERvooRT, GARY WILLIAMS, JEANETTE E. Watson, DENNIS M. OPREsko, PETER SCHUCHERT, P. MICHAEL HINE, DENNIS P. GORDON, HAMISH J. CAMPBELL, ANTHONY J. WRIGHT, JUAN A. SÁNCHEZ, DAPHNE G. FAUTIN his ancient phylum of mostly marine organisms is best known for its contribution to geomorphological features, forming thousands of square Tkilometres of coral reefs in warm tropical waters. Their fossil remains contribute to some limestones. Cnidarians are also significant components of the plankton, where large medusae – popularly called jellyfish – and colonial forms like Portuguese man-of-war and stringy siphonophores prey on other organisms including small fish. Some of these species are justly feared by humans for their stings, which in some cases can be fatal. Certainly, most New Zealanders will have encountered cnidarians when rambling along beaches and fossicking in rock pools where sea anemones and diminutive bushy hydroids abound. In New Zealand’s fiords and in deeper water on seamounts, black corals and branching gorgonians can form veritable trees five metres high or more. In contrast, inland inhabitants of continental landmasses who have never, or rarely, seen an ocean or visited a seashore can hardly be impressed with the Cnidaria as a phylum – freshwater cnidarians are relatively few, restricted to tiny hydras, the branching hydroid Cordylophora, and rare medusae. Worldwide, there are about 10,000 described species, with perhaps half as many again undescribed. All cnidarians have nettle cells known as nematocysts (or cnidae – from the Greek, knide, a nettle), extraordinarily complex structures that are effectively invaginated coiled tubes within a cell.