Coral Compatibility Guide – Large Polyped Stony (LPS) – Page 1
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Response of Fluorescence Morphs of the Mesophotic Coral Euphyllia Paradivisa to Ultra-Violet Radiation
www.nature.com/scientificreports OPEN Response of fuorescence morphs of the mesophotic coral Euphyllia paradivisa to ultra-violet radiation Received: 23 August 2018 Or Ben-Zvi 1,2, Gal Eyal 1,2,3 & Yossi Loya 1 Accepted: 15 March 2019 Euphyllia paradivisa is a strictly mesophotic coral in the reefs of Eilat that displays a striking color Published: xx xx xxxx polymorphism, attributed to fuorescent proteins (FPs). FPs, which are used as visual markers in biomedical research, have been suggested to serve as photoprotectors or as facilitators of photosynthesis in corals due to their ability to transform light. Solar radiation that penetrates the sea includes, among others, both vital photosynthetic active radiation (PAR) and ultra-violet radiation (UVR). Both types, at high intensities, are known to have negative efects on corals, ranging from cellular damage to changes in community structure. In the present study, fuorescence morphs of E. paradivisa were used to investigate UVR response in a mesophotic organism and to examine the phenomenon of fuorescence polymorphism. E. paradivisa, although able to survive in high-light environments, displayed several physiological and behavioral responses that indicated severe light and UVR stress. We suggest that high PAR and UVR are potential drivers behind the absence of this coral from shallow reefs. Moreover, we found no signifcant diferences between the diferent fuorescence morphs’ responses and no evidence of either photoprotection or photosynthesis enhancement. We therefore suggest that FPs in mesophotic corals might have a diferent biological role than that previously hypothesized for shallow corals. Te solar radiation that reaches the earth’s surface includes, among others, ultra-violet radiation (UVR; 280– 400 nm) and photosynthetically active radiation (PAR; 400–700 nm). -
Resurrecting a Subgenus to Genus: Molecular Phylogeny of Euphyllia and Fimbriaphyllia (Order Scleractinia; Family Euphylliidae; Clade V)
Resurrecting a subgenus to genus: molecular phylogeny of Euphyllia and Fimbriaphyllia (order Scleractinia; family Euphylliidae; clade V) Katrina S. Luzon1,2,3,*, Mei-Fang Lin4,5,6,*, Ma. Carmen A. Ablan Lagman1,7, Wilfredo Roehl Y. Licuanan1,2,3 and Chaolun Allen Chen4,8,9,* 1 Biology Department, De La Salle University, Manila, Philippines 2 Shields Ocean Research (SHORE) Center, De La Salle University, Manila, Philippines 3 The Marine Science Institute, University of the Philippines, Quezon City, Philippines 4 Biodiversity Research Center, Academia Sinica, Taipei, Taiwan 5 Department of Molecular and Cell Biology, James Cook University, Townsville, Australia 6 Evolutionary Neurobiology Unit, Okinawa Institute of Science and Technology Graduate University, Okinawa, Japan 7 Center for Natural Sciences and Environmental Research (CENSER), De La Salle University, Manila, Philippines 8 Taiwan International Graduate Program-Biodiversity, Academia Sinica, Taipei, Taiwan 9 Institute of Oceanography, National Taiwan University, Taipei, Taiwan * These authors contributed equally to this work. ABSTRACT Background. The corallum is crucial in building coral reefs and in diagnosing systematic relationships in the order Scleractinia. However, molecular phylogenetic analyses revealed a paraphyly in a majority of traditional families and genera among Scleractinia showing that other biological attributes of the coral, such as polyp morphology and reproductive traits, are underutilized. Among scleractinian genera, the Euphyllia, with nine nominal species in the Indo-Pacific region, is one of the groups Submitted 30 May 2017 that await phylogenetic resolution. Multiple genetic markers were used to construct Accepted 31 October 2017 Published 4 December 2017 the phylogeny of six Euphyllia species, namely E. ancora, E. divisa, E. -
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. -
Scleractinia Fauna of Taiwan I
Scleractinia Fauna of Taiwan I. The Complex Group 台灣石珊瑚誌 I. 複雜類群 Chang-feng Dai and Sharon Horng Institute of Oceanography, National Taiwan University Published by National Taiwan University, No.1, Sec. 4, Roosevelt Rd., Taipei, Taiwan Table of Contents Scleractinia Fauna of Taiwan ................................................................................................1 General Introduction ........................................................................................................1 Historical Review .............................................................................................................1 Basics for Coral Taxonomy ..............................................................................................4 Taxonomic Framework and Phylogeny ........................................................................... 9 Family Acroporidae ............................................................................................................ 15 Montipora ...................................................................................................................... 17 Acropora ........................................................................................................................ 47 Anacropora .................................................................................................................... 95 Isopora ...........................................................................................................................96 Astreopora ......................................................................................................................99 -
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 -
Symbiodinium—Invertebrate Symbioses and the Role of Metabolomics
Mar. Drugs 2010, 8, 2546-2568; doi:10.3390/md8102546 OPEN ACCESS Marine Drugs ISSN 1660-3397 www.mdpi.com/journal/marinedrugs Review Symbiodinium—Invertebrate Symbioses and the Role of Metabolomics Benjamin R. Gordon 1,* and William Leggat 2,3 1 AIMS@JCU, Australian Institute of Marine Science, School of Pharmacy and Molecular Sciences, James Cook University, Townsville, Queensland 4811, Australia 2 ARC Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, Queensland 4811, Australia; E-Mail: [email protected] 3 School of Pharmacy and Molecular Sciences, James Cook University, Townsville, Queensland 4811, Australia * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +61-7-47815395; Fax: +61-7-47816078. Received: 26 August 2010; in revised form: 24 September 2010 / Accepted: 26 September 2010 / Published: 30 September 2010 Abstract: Symbioses play an important role within the marine environment. Among the most well known of these symbioses is that between coral and the photosynthetic dinoflagellate, Symbiodinium spp. Understanding the metabolic relationships between the host and the symbiont is of the utmost importance in order to gain insight into how this symbiosis may be disrupted due to environmental stressors. Here we summarize the metabolites related to nutritional roles, diel cycles and the common metabolites associated with the invertebrate-Symbiodinium relationship. We also review the more obscure metabolites and toxins that have been identified through natural products and biomarker research. Finally, we discuss the key role that metabolomics and functional genomics will play in understanding these important symbioses. Keywords: metabolomics; zooxanthellae; marine; Symbiodinium; coral 1. -
Diel Patterns of Larval Release by Five Brooding Scleractinian Corals
MARINE ECOLOGY PROGRESS SERIES Vol. 321: 133–142, 2006 Published September 8 Mar Ecol Prog Ser Diel patterns of larval release by five brooding scleractinian corals Tung-Yung Fan1, 2,*, Ke-Han Lin1, 3, Fu-Wen Kuo1, Keryea Soong3, Li-Lian Liu3, Lee-Shing Fang1, 2 1National Museum of Marine Biology and Aquarium, Pingtung, Taiwan 944, ROC 2Institute of Marine Biodiversity and Evolution, National Dong Hwa University, Hualien, Taiwan 974, ROC 3Institute of Marine Biology, National Sun Yat-Sen University, Kaohsiung, Taiwan 804, ROC ABSTRACT: Timing of larval release in benthic marine invertebrates plays an important role in determining the reproductive success and extent of larval dispersal. Few studies have been conducted on diel variations in planula release by corals. Five brooding corals Seriatopora hystrix, Stylophora pistillata, Pocillopora damicornis, Euphyllia glabrescens, and Tubastraea aurea in Nan- wan Bay, southern Taiwan, were selected to compare diel patterns of planula release. Corals were collected from the field and maintained in outdoor, flow-through systems to quantify the hourly release of planulae. Planulation by S. hystrix and S. pistillata was highly synchronized with 1 peak of planula release occurring close to sunrise. Planulae of P. damicornis and E. glabrescens were released throughout the day, and usually 2 peaks occurred in the early morning and at night. Planu- lation of the ahermatypic coral T. aurea occurred throughout the day without a consistent peak. The diel cycle of planulation for all 3 pocilloporids and E. glabrescens suggests that the light-dark cycle may be the cue that induces planula release. The majority of planulae of these 4 species being released in the dark might be beneficial for minimizing predation effects. -
Jan 2021 ZSL Stocklist.Pdf (699.26
Zoological Society of London - January 2021 stocklist ZSL LONDON ZOO Status at 01.01.2021 m f unk Invertebrata Aurelia aurita * Moon jellyfish 0 0 150 Pachyclavularia violacea * Purple star coral 0 0 1 Tubipora musica * Organ-pipe coral 0 0 2 Pinnigorgia sp. * Sea fan 0 0 20 Sarcophyton sp. * Leathery soft coral 0 0 5 Sinularia sp. * Leathery soft coral 0 0 18 Sinularia dura * Cabbage leather coral 0 0 4 Sinularia polydactyla * Many-fingered leather coral 0 0 3 Xenia sp. * Yellow star coral 0 0 1 Heliopora coerulea * Blue coral 0 0 12 Entacmaea quadricolor Bladdertipped anemone 0 0 1 Epicystis sp. * Speckled anemone 0 0 1 Phymanthus crucifer * Red beaded anemone 0 0 11 Heteractis sp. * Elegant armed anemone 0 0 1 Stichodactyla tapetum Mini carpet anemone 0 0 1 Discosoma sp. * Umbrella false coral 0 0 21 Rhodactis sp. * Mushroom coral 0 0 8 Ricordea sp. * Emerald false coral 0 0 19 Acropora sp. * Staghorn coral 0 0 115 Acropora humilis * Staghorn coral 0 0 1 Acropora yongei * Staghorn coral 0 0 2 Montipora sp. * Montipora coral 0 0 5 Montipora capricornis * Coral 0 0 5 Montipora confusa * Encrusting coral 0 0 22 Montipora danae * Coral 0 0 23 Montipora digitata * Finger coral 0 0 6 Montipora foliosa * Hard coral 0 0 10 Montipora hodgsoni * Coral 0 0 2 Pocillopora sp. * Cauliflower coral 0 0 27 Seriatopora hystrix * Bird nest coral 0 0 8 Stylophora sp. * Cauliflower coral 0 0 1 Stylophora pistillata * Pink cauliflower coral 0 0 23 Catalaphyllia jardinei * Elegance coral 0 0 4 Euphyllia ancora * Crescent coral 0 0 4 Euphyllia glabrescens * Joker's cap coral 0 0 2 Euphyllia paradivisa * Branching frog spawn 0 0 3 Euphyllia paraancora * Branching hammer coral 0 0 3 Euphyllia yaeyamaensis * Crescent coral 0 0 4 Plerogyra sinuosa * Bubble coral 0 0 1 Duncanopsammia axifuga + Coral 0 0 2 Tubastraea sp. -
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. -
Tonga (866) 874-7639 (855) 225-8086
American Ingenuity www.livestockusa.org Tonga (866) 874-7639 (855) 225-8086 Wednesday to LAX, Thursday to you Tranship - F.O.B. Tonga Order Cut-off is on Thursdays! Animal cost plus landing costs "Poor man's Australia!" See landing costs below Acros, Montis, and Euphys are especially awesome! Demand is very heavy, order early! August 11, 2021 Note: List comes to us directly from Tonga Next shipment will be mid-late August Order Code Genus or binomial Common Name Cost HARD CORALS CH-ACANAS Acanthastrea echinata Acanthastrea $41.00 CH-ACANAS Acanthastrea Bowerbanki Acanthastrea $55.00 CH-ACROGR Acropora sp Green Acropora $55.00 CH-ACROPK Acropora sp Pink Acropora Millepora $55.00 CH-ACROPU Acropora sp Purple Acropora $55.00 CH-ACROYL Acropora sp Yellow Acropora $55.00 CH-ACROBL Acropora sp Blue Acropora $55.00 CH-ACROTR Acropora sp Tri-colored Acropora $55.00 CH-ASTRAS Astreopora sp Astreopora $27.00 CH-BLASTO Blastomussa sp Blastomussa $60.00 CH-CAULAS Caulastrea sp Candycane Coral $27.00 CH-CYNAAS Cynarina Lacrymalis Button Coral $37.50 CH-CYPHAS Cyphastrea sp Cyphastrea $27.00 CH-ECHINO Echinophyllia sp Echinophyllia $55.00 CH-EUPHHM Euphyllia Cristata Torch Coral - Grape $55.00 CH-EUPHGT Euphyllia paradivisa Frogspawn $50.00 CH-EUPHYT Euphyllia paradivisa Frogspawn $50.00 CH-EUPHAT Euphyllia Glabrescens Torch Coral $50.00 CH-EUPHMG Euphyllia Glabrescens Torch Coral - Green Metallic $55.00 Euphyllia GOLD TORCH ( Available sometimes ) $90.00 CH-EUPHPAR Euphyllia Paranacora Hammer Coral $58.00 CH-FAVYEL Favia sp Favia - Yellow $27.00 CH-FAVCOL -
Complete Mitochondrial Genome of Echinophyllia Aspera (Scleractinia
A peer-reviewed open-access journal ZooKeys 793: 1–14 (2018) Complete mitochondrial genome of Echinophyllia aspera... 1 doi: 10.3897/zookeys.793.28977 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Complete mitochondrial genome of Echinophyllia aspera (Scleractinia, Lobophylliidae): Mitogenome characterization and phylogenetic positioning Wentao Niu1, Shuangen Yu1, Peng Tian1, Jiaguang Xiao1 1 Laboratory of Marine Biology and Ecology, Third Institute of Oceanography, State Oceanic Administration, Xiamen, China Corresponding author: Wentao Niu ([email protected]) Academic editor: B.W. Hoeksema | Received 9 August 2018 | Accepted 20 September 2018 | Published 29 October 2018 http://zoobank.org/8CAEC589-89C7-4D1D-BD69-1DB2416E2371 Citation: Niu W, Yu S, Tian P, Xiao J (2018) Complete mitochondrial genome of Echinophyllia aspera (Scleractinia, Lobophylliidae): Mitogenome characterization and phylogenetic positioning. ZooKeys 793: 1–14. https://doi. org/10.3897/zookeys.793.28977 Abstract Lack of mitochondrial genome data of Scleractinia is hampering progress across genetic, systematic, phy- logenetic, and evolutionary studies concerning this taxon. Therefore, in this study, the complete mitog- enome sequence of the stony coral Echinophyllia aspera (Ellis & Solander, 1786), has been decoded for the first time by next generation sequencing and genome assembly. The assembled mitogenome is 17,697 bp in length, containing 13 protein coding genes (PCGs), two transfer RNAs and two ribosomal RNAs. It has the same gene content and gene arrangement as in other Scleractinia. All genes are encoded on the same strand. Most of the PCGs use ATG as the start codon except for ND2, which uses ATT as the start codon. The A+T content of the mitochondrial genome is 65.92% (25.35% A, 40.57% T, 20.65% G, and 13.43% for C). -
Contrasting Patterns of Changes in Abundance Following a Bleaching Event Between Juvenile and Adult Scleractinian Corals
Coral Reefs (2018) 37:527–532 https://doi.org/10.1007/s00338-018-1677-y NOTE Contrasting patterns of changes in abundance following a bleaching event between juvenile and adult scleractinian corals 1,2 2 2,3 Mariana A´ lvarez-Noriega • Andrew H. Baird • Tom C. L. Bridge • 4 5 6 5 Maria Dornelas • Luisa Fontoura • Oscar Pizarro • Kristin Precoda • 5 5 4,5 5 Damaris Torres-Pulliza • Rachael M. Woods • Kyle Zawada • Joshua S. Madin Received: 21 September 2017 / Accepted: 14 March 2018 / Published online: 19 March 2018 Ó Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Coral bleaching events have caused extensive Acropora and Goniastrea were less susceptible to bleach- mortality on reefs around the world. Juvenile corals are ing than adults, but the opposite was true for Pocillopora generally less affected by bleaching than their conspecific spp. and taxa in the family Merulinidae. Our results indi- adults and therefore have the potential to buffer population cate that the potential of the juvenile life stage to act as a declines and seed recovery. Here, we use juvenile and adult buffer during bleaching events is taxon-dependent. abundance data at 20 sites encircling Lizard Island, Great Barrier Reef, before and after the 2016 bleaching event to Keywords Coral reefs Á Climate change Á Ecology Á quantify: (1) correlates of changes in juvenile abundance Thermal stress Á Juvenile corals following a bleaching event; (2) differences in suscepti- bility to extreme thermal stress between juveniles and adults. Declines in juvenile abundance were lower at sites Introduction closer to the 20-m-depth contour and higher for Acropora and Pocillopora juveniles than for other taxa.