A Mass Mortality of <I>Gorgonia Ventalina</I>
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Coral Diversity and Disease in Mexico
DISEASES OF AQUATIC ORGANISMS Vol. 69: 23–31, 2006 Published March 23 Dis Aquat Org Coral diversity and disease in Mexico J. R. Ward1,*, K. L. Rypien1, J. F. Bruno2, C. D. Harvell1, E. Jordán-Dahlgren3, K. M. Mullen4, R. E. Rodríguez-Martínez3, J. Sánchez5, G. Smith6 1Department of Ecology and Evolutionary Biology, Corson Hall, Cornell University, Ithaca, New York 14853, USA 2Department of Marine Sciences, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3300, USA 3Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, Apdo. Postal 1152, Cancún, 77500, Quintana Roo, Mexico 4Department of Entomology, Comstock Hall, Cornell University, Ithaca, New York 14853, USA 5Departamento de Ciencias Biológicas, Universidad de los Andes, Carrera 1E No 18A-10, Bogotá, Colombia 6Department of Biology and Geology, 471 University Parkway, Aiken, South Carolina 29801, USA ABSTRACT: Field studies and empirical tests of the ‘diversity-disease hypothesis’ demonstrate the effects of species richness on disease transmission and severity in plant systems. Yet the converse, i.e. effects of disease on diversity, is rarely considered in either relatively well-studied plant systems or marine ecosystems. We investigated these effects along the Mexican Yucatan Peninsula to (1) quan- tify the relationship between disease prevalence and coral diversity, (2) test the hypothesis that octo- coral and scleractinian disease prevalence are associated with one another, and (3) establish a long- term dataset. Aspergillosis of sea fans and 6 scleractinian diseases were documented. Prevalence of aspergillosis declined from 12.85% in 2002 to 5.26% in 2004, while prevalence of scleractinian dis- eases remained relatively constant at 5.7 ± 0.8% in 2002 and 7.96 ± 0.7% in 2004. -
Gonian Eunicella Singularis (Esper, 1791) (Anthozoa Gorgoni - Idae) of Paloma Island, Algeria
Biodiversity Journal , 2019, 10 (3): 185–194 https://doi.org/ 10.31396/Biodiv.Jour.2019.10.3.185.194 Morphometric data and allometric relationships of the gor - gonian Eunicella singularis (Esper, 1791) (Anthozoa Gorgoni - idae) of Paloma Island, Algeria Mouloud Benabdi 1, Lalla A. T. Cherif-Louazani 1, Alae Eddine Belmahi 1, Samir Grimes 2, Yassine G.E. Khames 3, Billel Boufekane 3, Salim Mouffok 1 & Mohamed Bouderbala 1 1Laboratoire Réseau de Surveillance Environnementale, Faculté SNV, Université Oran1, Algeria 2École Nationale Supérieure des Sciences de la Mer et de l’Aménagement du Littoral Alger, Algeria 3Faculté des Sciences Biologiques, USTHB, Alger, Algeria *Corresponding author, email: [email protected] ABSTRACT The gorgonian Eunicella singularis (Esper, 1791) (Anthozoa Gorgoniidae) is abundant on rocky bottoms at Paloma Island (Algeria) in the south-western of the Mediterranean basin. In this study area, 150 gorgonian colonies of E. singularis were collected randomly using SCUBA diving and the following morphometric macro-features were measured (maximum height, maximum width, total branch length, rectangular surface area, height to width ratio and dry weight). Allometric growth was examined using the relationships between the dry weight and the five morphometric macro-features. The power equation of the simple allometry applied was y=ax b and the parameters of the linear regression a and b were estimated after the logarithmic transformation log (y)=log( a)+ b*log(x). The allometric relationships between the dry weight and the morphometric macro-features studied show that the growth of the gor - gonian E. singularis in the study area is correlated positively and significantly with the five macro-features and that both the macro-features total branch length and the maximum width are the most appropriate parameter applied to the gorgonian E. -
Microbiomes of Gall-Inducing Copepod Crustaceans from the Corals Stylophora Pistillata (Scleractinia) and Gorgonia Ventalina
www.nature.com/scientificreports OPEN Microbiomes of gall-inducing copepod crustaceans from the corals Stylophora pistillata Received: 26 February 2018 Accepted: 18 July 2018 (Scleractinia) and Gorgonia Published: xx xx xxxx ventalina (Alcyonacea) Pavel V. Shelyakin1,2, Sofya K. Garushyants1,3, Mikhail A. Nikitin4, Sofya V. Mudrova5, Michael Berumen 5, Arjen G. C. L. Speksnijder6, Bert W. Hoeksema6, Diego Fontaneto7, Mikhail S. Gelfand1,3,4,8 & Viatcheslav N. Ivanenko 6,9 Corals harbor complex and diverse microbial communities that strongly impact host ftness and resistance to diseases, but these microbes themselves can be infuenced by stresses, like those caused by the presence of macroscopic symbionts. In addition to directly infuencing the host, symbionts may transmit pathogenic microbial communities. We analyzed two coral gall-forming copepod systems by using 16S rRNA gene metagenomic sequencing: (1) the sea fan Gorgonia ventalina with copepods of the genus Sphaerippe from the Caribbean and (2) the scleractinian coral Stylophora pistillata with copepods of the genus Spaniomolgus from the Saudi Arabian part of the Red Sea. We show that bacterial communities in these two systems were substantially diferent with Actinobacteria, Alphaproteobacteria, and Betaproteobacteria more prevalent in samples from Gorgonia ventalina, and Gammaproteobacteria in Stylophora pistillata. In Stylophora pistillata, normal coral microbiomes were enriched with the common coral symbiont Endozoicomonas and some unclassifed bacteria, while copepod and gall-tissue microbiomes were highly enriched with the family ME2 (Oceanospirillales) or Rhodobacteraceae. In Gorgonia ventalina, no bacterial group had signifcantly diferent prevalence in the normal coral tissues, copepods, and injured tissues. The total microbiome composition of polyps injured by copepods was diferent. -
St. Kitts Final Report
ReefFix: An Integrated Coastal Zone Management (ICZM) Ecosystem Services Valuation and Capacity Building Project for the Caribbean ST. KITTS AND NEVIS FIRST DRAFT REPORT JUNE 2013 PREPARED BY PATRICK I. WILLIAMS CONSULTANT CLEVERLY HILL SANDY POINT ST. KITTS PHONE: 1 (869) 765-3988 E-MAIL: [email protected] 1 2 TABLE OF CONTENTS Page No. Table of Contents 3 List of Figures 6 List of Tables 6 Glossary of Terms 7 Acronyms 10 Executive Summary 12 Part 1: Situational analysis 15 1.1 Introduction 15 1.2 Physical attributes 16 1.2.1 Location 16 1.2.2 Area 16 1.2.3 Physical landscape 16 1.2.4 Coastal zone management 17 1.2.5 Vulnerability of coastal transportation system 19 1.2.6 Climate 19 1.3 Socio-economic context 20 1.3.1 Population 20 1.3.2 General economy 20 1.3.3 Poverty 22 1.4 Policy frameworks of relevance to marine resource protection and management in St. Kitts and Nevis 23 1.4.1 National Environmental Action Plan (NEAP) 23 1.4.2 National Physical Development Plan (2006) 23 1.4.3 National Environmental Management Strategy (NEMS) 23 1.4.4 National Biodiversity Strategy and Action Plan (NABSAP) 26 1.4.5 Medium Term Economic Strategy Paper (MTESP) 26 1.5 Legislative instruments of relevance to marine protection and management in St. Kitts and Nevis 27 1.5.1 Development Control and Planning Act (DCPA), 2000 27 1.5.2 National Conservation and Environmental Protection Act (NCEPA), 1987 27 1.5.3 Public Health Act (1969) 28 1.5.4 Solid Waste Management Corporation Act (1996) 29 1.5.5 Water Courses and Water Works Ordinance (Cap. -
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. -
Immune Response of the Caribbean Sea Fan, Gorgonia Ventalina, Exposed to an Aplanochytrium Parasite As Revealed by Transcriptome Sequencing
ORIGINAL RESEARCH ARTICLE published: 25 July 2013 doi: 10.3389/fphys.2013.00180 Immune response of the Caribbean sea fan, Gorgonia ventalina, exposed to an Aplanochytrium parasite as revealed by transcriptome sequencing Colleen A. Burge 1*, Morgan E. Mouchka 1,C.DrewHarvell1 and Steven Roberts 2 1 Department of Ecology and Evolutionary Biology, Cornell University, Ithaca, NY, USA 2 School of Aquatic and Fishery Sciences, University of Washington, Seattle, WA, USA Edited by: Coral reef communities are undergoing marked declines due to a variety of stressors Sassan Asgari, The University of including disease. The sea fan coral, Gorgonia ventalina, is a tractable study system Queensland, Australia to investigate mechanisms of immunity to a naturally occurring pathogen. Functional Reviewed by: studies in Gorgonia ventalina immunity indicate that several key pathways and cellular David A. Raftos, Macquarie University, Australia components are involved in response to natural microbial invaders, although to date Sandie M. Degnan, The University the functional and regulatory pathways remain largely un-described. This study used of Queensland, Australia short-read sequencing (Illumina GAIIx) to identify genes involved in the response of G. *Correspondence: ventalina to a naturally occurring Aplanochytrium spp. parasite. De novo assembly of Colleen A. Burge, Department of the G. ventalina transcriptome yielded 90,230 contigs of which 40,142 were annotated. Ecology and Evolutionary Biology, Cornell University, E343 Corson RNA-Seq analysis revealed 210 differentially expressed genes in sea fans exposed to Hall, Ithaca, NY 14853, USA the Aplanochytrium parasite. Differentially expressed genes involved in immunity include e-mail: [email protected] pattern recognition molecules, anti-microbial peptides, and genes involved in wound repair and reactive oxygen species formation. -
Cnidaria: Octocorallia: Gorgoniidae) from Mesophotic Reefs in the Eastern Pacific
BULLETIN OF MARINE SCIENCE. 89(3):735–743. 2013 NEW TAXA PAPER http://dx.doi.org/10.5343/bms.2013.1014 http://zoobank.org/urn:lsid:zoobank.org:pub:E62C6099-A6E3-43E0-8F43-014ED71DA0D5 A NEW SPECIES OF THE GENUS EUGORGIA (CNIDARIA: OCTOCORALLIA: GORGONIIDAE) FROM MESOPHOTIC REEFS IN THE EASTERN PACIFIC Odalisca Breedy and Hector M Guzman ABSTRACT Our knowledge of octocoral diversity in the eastern Pacific has been focused on shallow reef habitats, while the fauna occurring in the mesophotic zone from 40 to 150 m is poorly known. A new species of the gorgoniid Eugorgia was recently obtained with a submersible from the Hannibal Bank, a coastal seamount 60 km off mainland Panama and 15 km from Coiba Island. The morphological characters were analyzed and illustrated by light and scanning electron microscopy. Eugorgia siedenburgae sp. nov. can be distinguished from the other species in the genus by its bushy, multiplanar, bicolored colony, and the sclerites colors, composition, and sizes. This new species increases the number in the genus to 13 and contributes to our understanding of the fragile mesophotic biodiversity. Octocoral diversity surveys in the eastern Pacific region have been focused mainly on shallow environments to 40 m depth (e.g., Williams and Breedy 2004, Breedy et al. 2009, Breedy and Guzman 2012). Consequently, the fauna inhabiting mesophotic habitats from 40 m to >150 m is poorly described and may be at risk due to intensive fishing (see Lesser et al. 2009, Clark et al. 2010). Here, we describe a new species of the gorgoniid Eugorgia recently collected from the Hannibal Bank seamount, Pacific Panama. -
Rangewide Population Genetic Structure of the Caribbean Sea Fan
Molecular Ecology (2013) 22, 56–73 doi: 10.1111/mec.12104 Range-wide population genetic structure of the Caribbean sea fan coral, Gorgonia ventalina JASON P. ANDRAS,* KRYSTAL L. RYPIEN† and CATHERINE D. HARVELL Department of Ecology and Evolutionary Biology, Cornell University, Dale R. Corson Hall, Ithaca, NY 14853, USA Abstract The population structure of benthic marine organisms is of central relevance to the conservation and management of these often threatened species, as well as to the accurate understanding of their ecological and evolutionary dynamics. A growing body of evidence suggests that marine populations can be structured over short dis- tances despite theoretically high dispersal potential. Yet the proposed mechanisms governing this structure vary, and existing empirical population genetic evidence is of insufficient taxonomic and geographic scope to allow for strong general inferences. Here, we describe the range-wide population genetic structure of an ecologically important Caribbean octocoral, Gorgonia ventalina. Genetic differentiation was posi- tively correlated with geographic distance and negatively correlated with oceanograph- ically modelled dispersal probability throughout the range. Although we observed admixture across hundreds of kilometres, estimated dispersal was low, and popula- tions were differentiated across distances <2 km. These results suggest that popula- tions of G. ventalina may be evolutionarily coupled via gene flow but are largely demographically independent. Observed patterns of differentiation corroborate biogeographic breaks found in other taxa (e.g. an east/west divide near Puerto Rico), and also identify population divides not discussed in previous studies (e.g. the Yucatan Channel). High genotypic diversity and absence of clonemates indicate that sex is the primary reproductive mode for G. -
California State University, Northridge an Ecological
CALIFORNIA STATE UNIVERSITY, NORTHRIDGE AN ECOLOGICAL AND PHYSIOLOGICAL ASSESSMENT OF TROPICAL CORAL REEF RESPONSES TO PAST AND PROJECTED DISTURBANCES A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Biology By Elizabeth Ann Lenz May 2014 The thesis of Elizabeth A. Lenz is approved by: Robert C. Carpenter, Ph.D. Date: Eric D. Sanford, Ph.D. Date: Mark A. Steele, Ph.D. Date: Peter J. Edmunds, Ph.D., Chair Date: California State University, Northridge ii ACKNOWLEDGEMENTS I would like to thank Dr. Peter J. Edmunds first and foremost for being my fearless leader and advisor - for the incredible opportunities and invaluable mentorship he has provided to me as a graduate student in the Polyp Lab. I am ever so grateful for his guidance, endless caffeinated energy, constructive critiques, and dry British humor. I would also like to thank my loyal committee members Drs. Robert Carpenter and Mark Steele at CSUN for their availability and expert advise during this process. Their suggestions have greatly contributed to my thesis. I would not only like to acknowledge Dr. Eric Sanford from UC Davis for serving on my committee, but thank him for his incessant support throughout my career over the last 7 years. I will always admire his contagious enthusiasm for invertebrates, passion for scientific research, and unlimited knowledge about marine ecology. My research would not have been possible without the technical support and assistance from my colleagues in Moorea, French Polynesia and St. John, USVI. I am grateful to Dr. Lorenzo Bramanti, Dr. Steeve Comeau, Vince Moriarty, Nate Spindel, Emily Rivest, Christopher Wall, Darren Brown, Alexandre Yarid, Nicolas Evensen, Craig Didden, the VIERS staff, and undergraduate assistants: Kristin Privitera-Johnson and Amanda Arnold. -
Cnidarian Immunity and the Repertoire of Defense Mechanisms in Anthozoans
biology Review Cnidarian Immunity and the Repertoire of Defense Mechanisms in Anthozoans Maria Giovanna Parisi 1,* , Daniela Parrinello 1, Loredana Stabili 2 and Matteo Cammarata 1,* 1 Department of Earth and Marine Sciences, University of Palermo, 90128 Palermo, Italy; [email protected] 2 Department of Biological and Environmental Sciences and Technologies, University of Salento, 73100 Lecce, Italy; [email protected] * Correspondence: [email protected] (M.G.P.); [email protected] (M.C.) Received: 10 August 2020; Accepted: 4 September 2020; Published: 11 September 2020 Abstract: Anthozoa is the most specious class of the phylum Cnidaria that is phylogenetically basal within the Metazoa. It is an interesting group for studying the evolution of mutualisms and immunity, for despite their morphological simplicity, Anthozoans are unexpectedly immunologically complex, with large genomes and gene families similar to those of the Bilateria. Evidence indicates that the Anthozoan innate immune system is not only involved in the disruption of harmful microorganisms, but is also crucial in structuring tissue-associated microbial communities that are essential components of the cnidarian holobiont and useful to the animal’s health for several functions including metabolism, immune defense, development, and behavior. Here, we report on the current state of the art of Anthozoan immunity. Like other invertebrates, Anthozoans possess immune mechanisms based on self/non-self-recognition. Although lacking adaptive immunity, they use a diverse repertoire of immune receptor signaling pathways (PRRs) to recognize a broad array of conserved microorganism-associated molecular patterns (MAMP). The intracellular signaling cascades lead to gene transcription up to endpoints of release of molecules that kill the pathogens, defend the self by maintaining homeostasis, and modulate the wound repair process. -
Spatial and Temporal Trends of Southeastern Florida's Octocoral Comunity
Nova Southeastern University NSUWorks HCNSO Student Theses and Dissertations HCNSO Student Work 12-6-2019 Spatial and Temporal Trends of Southeastern Florida's Octocoral Comunity Alexandra Hiley Nova Southeastern University Follow this and additional works at: https://nsuworks.nova.edu/occ_stuetd Part of the Marine Biology Commons, and the Oceanography and Atmospheric Sciences and Meteorology Commons Share Feedback About This Item NSUWorks Citation Alexandra Hiley. 2019. Spatial and Temporal Trends of Southeastern Florida's Octocoral Comunity. Master's thesis. Nova Southeastern University. Retrieved from NSUWorks, . (522) https://nsuworks.nova.edu/occ_stuetd/522. This Thesis is brought to you by the HCNSO Student Work at NSUWorks. It has been accepted for inclusion in HCNSO Student Theses and Dissertations by an authorized administrator of NSUWorks. For more information, please contact [email protected]. Thesis of Alexandra Hiley Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science M.S. Marine Biology Nova Southeastern University Halmos College of Natural Sciences and Oceanography December 2019 Approved: Thesis Committee Major Professor: David Gilliam, Ph.D. Committee Member: Rosanna Milligan, Ph.D. Committee Member: Charles Messing, Ph.D. This thesis is available at NSUWorks: https://nsuworks.nova.edu/occ_stuetd/522 Spatial and temporal trends in Southeastern Florida’s octocoral community By Alexandra Hiley Submitted to the Faculty of Halmos College of Natural Sciences and Oceanography in partial fulfillment of the requirements for the degree of Master of Science with a specialty in: Marine Biology Nova Southeastern University Halmos College of Natural Science and Oceanography Committee Members: David Gilliam, Ph.D. Charles Messing, Ph.D. -
Curriculum Vitae
CURRICULUM VITAE Elizabeth (Beth) Anne Horvath Education: --May, 1976, Bachelor of Arts, Biology--Westmont College --August, 1981, Masters of Science, Biology--Cal. State Univ., Long Beach Dissertation Title: Experiences in Marine Science, an Introductory Text. Supplemental Research Projects: Pelagic Snails; Development in Pelagic Tunicates; SEM studies of Luminescence in Pelagic Tunicates --Selected Graduate Level Courses beyond Master's; subjects include-- Channel Island Biology, Deep Sea Biology, Conservation Biology; also Field Course: Natural History of the Galapagos Islands (UCLA) Teaching Experience: (Emphases on: Marine Biology, Invertebrate Zoology, Marine Ecology and Natural History, Zoology, Marine Mammals) --Westmont College, 1978-1998, Part time to Full time Instructor --Santa Barbara City College, 1989-1990, Instructor (Human Anatomy) --Westmont College, 1998-2013, Assistant Professor; 2013-Present, Associate Professor --AuSable, Pacific Rim: Assistant/Associate Professor, 1998-2006; 2018-Present --CCSP-New Zealand: Associate Professor, Spring, 2010, Fall, 2011, Fall, 2012 Courses Created/Developed: (Undergraduate level, most Upper Division): Marine Biology, Invertebrate Zoology, Marine Invertebrates, Marine Mammals, Marine Mammal Ecophysiology, Animal Diversity, General Zoology Rank: First Year at Westmont: Instructor (part-Time), 1978; Full-Time, 1988 Previous Rank: Instructor of Biology, 1990-1998; Assistant Professor, 1998-2013 Present Rank: Associate Professor, Fall 2013 to the present Administrative Duties Have Included: