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  • 1
    Online Resource
    Online Resource
    Staghorn Corals of the World : A Revision of the Genus Acropora. (1999)
    Collingwood :CSIRO Publishing,
    Details
    Keywords: Electronic books.
    Description / Table of Contents: This invaluable reference tool is the first major review of Acropora in over 100 years.
    Type of Medium: Online Resource
    Pages: 1 online resource (657 pages)
    Edition: 1st ed.
    ISBN: 9780643101388
    URL: https://ebookcentral.proquest.com/lib/geomar/detail.action?docID=610609
    Language: English
    Note: Intro -- Title -- Copyright -- Dedication -- Foreword -- Abstract -- Acknowledgements -- Contents -- Introduction -- Review of Literature -- Nomenclatural history of the genus -- Type species -- Trends in the taxonomy of Acropora -- Classification -- Sub-generic classification -- Super-generic classification -- Summary of Type Material -- Background -- Designation of lectotypes -- France -- Germany -- America -- England -- Philippines -- Australia -- Africa -- Russia -- Austria -- Italy -- India -- Fossil Record -- Distribution of fossil assemblages -- Fossil species -- Anatomy, Physiology and Biology -- Soft structures -- Colouration -- Skeleton and growth -- Gastrovascular system -- Gonads -- General -- Female gonads and oocytes -- Testes and spermatozoa -- Sexual reproduction -- General -- Fertilisation and development -- Reproductive effort and fecundity -- Hybridisation -- Asexual reproduction -- Ecology -- General -- Zonation patterns -- Life histories -- Recruitment -- Maturation and senescence -- Mortality -- Associations and interactions -- Diseases -- Genetics and Molecular Biology -- General -- Chromosome number -- Genetic characters -- Evolutionary signature of hybridisation -- Skeletal Morphology -- General -- Terminology -- Recognition of juvenile Acropora colonies -- Colony form -- General -- Nomenclature of colony forms -- Corallites -- Axial corallites -- Radial corallites -- Coenosteum -- Variations in morphology -- Methods Used for Revision and Analyses -- The Worldwide Acropora Database -- Locations -- Sampling and database protocol -- Mapping of distributions for species descriptions -- Format of synonymies -- Citation of localities for material examined -- Characters used in descriptions of species -- Biogeographic analyses -- Phylogenetic analyses -- Development of a LucID interactive key -- Photo library of type specimens. , Revision of the Biogeography of Acropora -- Background -- Groupings of records -- Species composition of areas, regions and super regions -- Similarities between areas and regions -- Types of distributions exhibited by species -- Distribution characteristics of the fauna of areas and regions -- Revision of the Phylogeny and Classification of Acropora -- Background -- Methodology -- Taxa -- Characters -- Programs -- Phylogeny of the family Acroporidae -- Phylogeny of the genus Acropora -- Cladograms -- Clades -- Species groupings in the subgenus Acropora -- General -- Monophyletic groups -- Paraphyletic groups -- Misplaced species -- Patterns of character transformation in Acropora phylogeny -- General -- Colony form and branches -- Skeletal density -- Coenosteal characteristics -- Radial corallites -- Axial corallites -- Summary of transformations and relationships of species groups -- Synthesis of Biogeographic, Fossil and Phylogenetic Data -- Evidence for the origination and evolution of Acropora -- General -- Cladograms in terms of habitat -- Cladograms in terms of fossil history -- Cladograms in terms of the biogeographic patterns -- Chronology of the origination of clades -- Hypothesis -- Colour Plates -- Systematic Arrangement of Species -- Family Acroporidae Verrill, 1902 -- Genus Acropora Oken, 1815 -- Type Species Millepora Muricata Linneaus, 1758 -- Subgenus Acropora Oken, 1815 -- The Acropora rudis group -- Acropora (Acropora) rudis (Rehberg, 1892) -- Acropora (Acropora) variolosa (Klunzinger, 1879) -- Acropora (Acropora) austera (Dana, 1846) -- Acropora (Acropora) hernprichii (Ehrenberg, 1834) -- The Acropora humilis group -- Acropora (Acropora) humilis (Dana, 1846) -- Acropora (Acropora) globiceps (Dana, 1846) -- Acropora (Acropora) gemmifera (Brook, 1892) -- Acropora (Acropora) monticulosa (Briiggemann, 1879). , Acropora (Acropora) samoensis (Brook, 1891) -- Acropora (Acropora) digitifera (Dana, 1846) -- Acropora (Acropora) multiacuta Nemenzo, 1967 -- Acropora (Acropora) retusa (Dana, 1846) -- The Acropora nasuta group -- Acropora (Acropora) nasuta (Dana, 1846) -- Acropora (Acropora) cerealis (Dana, 1846) -- Acropora (Acropora) valida (Dana, 1846) -- Acropora (Acropora) arabensis Hodgson & -- Carpenter, 1995 -- Acropora (Acropora) secale (Studer, 1878) -- Acropora (Acropora) lutkeni Crossland, 1952 -- Acropora (Acropora) kimbeensis sp. nov. 146 -- The Acropora divaricata group -- llcropora (Acropora) divaricata (Dana, 1846) -- Acropora (Acropora) solitaryensis Veron & -- Wallace, 1984 -- Acropora (Acropora) kosurini Wallace, 1994 -- Acropora (Acropora) hoeksemai Wallace, 1997 -- Acropora (Acropora) clathrata (Brook, 1891) 158 -- The Acropora lovelli group -- Acropora (Acropora) lovelli Veron & -- Wallace, 1984 -- Acropora (Acropora) bushyensis Veron & -- Wallace, 1984 -- Acropora (Acropora) glauca (Brook, 1893) -- The Acropora verweyi group -- Acropora (Acropora) verweyi Veron & -- Wallace, 1984 -- The Acropora cervicornis group -- Acropora (Acropora) cervicornis (Lamarck, 1816) -- Acropora (Acropora) palmata (Lamarck, 1816) -- Acropora (Acropora) prolifera (Lamarck, 1816) -- The Acropora muricata group -- Acropora (Acropora) muricata (Linneaus, 1758) -- Acropora (Acropora) grandis (Brook, 1892) -- Acropora (Acropora) acwninata (Verrill, 1864) -- Acropora (Acropora) valenciennesi (Edwards & -- Baime, 1860) -- Acropora (Acropora) phamonis (Edwards & -- Bairne, 1860) -- The Acropora robusta group -- Acropora (Acropora) robusta (Dana, 1846) -- Acropora (Acropora) abrotanoides (Lamarck, 1816) -- Acropora (Acropora) palrmerae Wells, 195'1 -- Acropora (Acropora) intermedia (Brook, 1891) -- Acropora (Acropora) polystoma (Brook, 1891). , Acropora (Acropora) downingi sp. nov. -- Acropora (Acropora) listeri (Brook, 1893) -- Acropora (Acropora) sukarnoi Wallace, 1997 -- The Acropora togianensis group -- Acropora (Acropora) togianensis Wallace, 1997 -- The Acropora selago group -- Acropora (Acropora) selago (Studer, 1878) -- Acropora (Acropora) tenuis (Dana, 1846) -- Acropora (Acropora) eurystorna (Klunzinger, 1879) -- Acropora (Acropora) striata (Verrill, 1866) -- Acropora (Acropora) donei Veron & -- Wallace, 1984 -- Acropora (Acropora) yongei Veron & -- Wallace, 1984 -- Acropora (Acropora) loisetleae Wallace, 1994 -- Acropora (Acropora) dendrurn (Bassett-Smith, 1890) -- The Acropora aspera group -- Acropora (Acropora) aspera (Dana, 1846) -- Acropora (Acropora) pulchra (Brook, 1891) -- Acropora (Acropora) millepora (Ehrenberg, 1834) -- Acropora (Acropora) spathulata (Brook, 1891) -- Acropora (Acropora) spicifera (Dana, 1846) -- Acropora (Acropora) papillare Latypov, 1992 -- Acropora (Acropora) roseni sp. nov. -- The Acropora florida group -- Acropora (Acropora) florida (Dana, 1846) -- Acropora (Acropora) sarrnenlosa (Brook, 1892) -- The Acropora hyacinthus group -- Acropora (Acropora) hyacinthus (Dana, 1846) -- Acropora (Acropora) tanegashimensis Veron, 1990 -- Acropora (Acropora) anthocercis (Brook, 1893) -- Acropora (Acropora) cytherea (Dana, 1846) -- Acropora (Acropora) microclados (Ehrenberg, 1834) -- Acropora (Acropora) paniculala Verrill, 1902 -- Acropora (Acropora) indonesia Wallace, 1997 -- The Acropora latistella group -- Acropora (Acropora) latistella (Brook, 1892) -- Acropora (Acropora) subulata (Dana, 1846) -- Acropora (Acropora) nana (Studer, 1878) -- Acropora (Acropora) aculeus (Dana, 1846) -- The Acropora horrida group -- Acropora (Acropora) horrida (Dana, 1846) -- Acropora (Acropora) vaughani Wells, 1954 -- Acropora (Acropora) tortuosa (Dana, 1846). , Acropora (Acropora) abrolhosensis Veron, 1985 -- Acropora (Acropora) microphthatma (Verrill, 1869) -- Acropora (Acropora) kintyae Veron & -- Wallace, 1984 -- Acropora (Acropora) derawanensis Wallace, 1997 -- Acropora (Acropora) halmaherae Wallace & -- Wolstenbolme, 1998 -- The Acropora (Acropora) plumosa group -- Acropora (Acropora) plumosa Wallace & -- Wolstenholme, 1998 -- The Acropora elegans group -- Acropora (Acropora) elegans (Edwards & -- Haime, 1860) -- Acropora (Acropora) pichoni sp. nov. -- Acropora (Acropora) tenella (Brook, 1892) -- Acropora (Acropora) walindii sp. nov. -- Acropora (Acropora) canlenae Wells, 1985 -- Acropora (Acropora) torihalimeda Wallace, 1994 -- Acropora (Acropora) russelli Wallace, 1994 -- The Acropora toripes group -- Acropora (Acropora) loripes (Brook, 1892) -- Acropora (Acropora) squarrosa (Eherenberg, 1834) -- Acropora (Acropora) chesterfieldensis Veron & -- Wallace, 1984 -- Acropora (Acropora) willisae Veron & -- Wallace, 1984 -- Acropora (Acropora) lokani Wallace, 1994 -- Acropora (Acropora) granulosa (Edwards & -- Haime, 1860) -- Acropora (Acropora) speciosa (Quelch, 1886) -- Acropora (Acropora) suharsonoi Wallace, 1994 -- Acropora (Acropora) caroliniana Nemenzo, 1976 -- Acropora (Acropora) desalwii Wallace, 1994 -- Acropora (Acropora) jacquelineae Wallace, 1994 -- Acropora (Acropora) simplex Wallace & -- Wolstenholme, 1998 -- The Acropora echinata group -- Acropora (Acropora) echinata (Dana, 1846) -- Acropora (Acropora) batunai Wallace, 1997 -- Acropora (Acropora) subglabra (Brook, 1891) -- Acropora (Acropora) carduus (Dana, 1846) -- Acropora (Acropora) awi Wallace & -- Wolstenholme, 1998 -- Acropora (Acropora) elseyi (Brook, 1892) -- Acropora (Acropora) longicyathus (Edwards & -- Haime, 1860) -- Acropora (Acropora) turaki Wallace, 1994 -- Subgenus Isopora Studer, 1878. , Acropora (Isopora) palifera (Lamarck, 1816).
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  • 2
    facet.materialart.
    Unknown
    (Table 4) Age analysis from different Holes of IODP Expedition 310 (2012)
    PANGAEA
    In:  Supplement to: Abbey, Elizabeth; Webster, Jody M; Braga, Juan-Carlos; Sugihara, Kaoru; Wallace, Carden; Iryu, Yasufumi; Potts, Donald C; Done, Terry; Camoin, Gilbert; Seard, Claire (2011): Variation in deglacial coralgal assemblages and their paleoenvironmental significance: IODP Expedition 310, “Tahiti Sea Level”. Global and Planetary Change, 76, 1-15, https://doi.org/10.1016/j.gloplacha.2010.11.005
    Details
    Publication Date: 2023-06-27
    Description: Fossil reefs are valuable recorders of paleoenvironmental changes during the last deglaciation, and detailed characterizations of coralgal assemblages can improve understanding of the behavior and impacts of sea-level rise. Drilling in 2005 by the Integrated Ocean Drilling Program (IODP) Expedition 310 explored submerged offshore reefs from three locations around Tahiti, French Polynesia and provides the first look at island-wide variability of coralgal assemblages during deglacial sea-level rise. We present the first detailed examination of coral and coralline algal taxonomy and morphology from two sites on Tahiti (offshore Tiarei and offshore Maraa). Sixteen cores ranging in depth from 122 m to 45 m below sea-level represent reef growth from 16 ka to ca. 8 ka (Camoin, G.F., Iryu, Y., McInroy, D.B. and the IODP Expedition 310 Scientists, 2007. IODP Expedition 310 reconstructs sea level, climatic, and environmental changes in the South Pacific during the last deglaciation. Scientific Drilling, 5: 4-12). Twenty-six coral species, twelve coral genera and twenty-eight coralline algal species were identified from 565 m of core and over 400 thin sections. Based on these data, and in comparison with modern and fossil analogs, seven coral and four algal assemblages have been identified in the deglacial sequences in Tahiti, representing a range of environments from less than 10 m to greater than 20-30 m water depth. Deglacial reef initiation varied at sites based on the available substrate, and early colonizers suggest water conditions at all sites were unfavorable to sensitive corals, such as Acropora, prior to ca. 12.5 ka. Mainly shallowwater (b10-15 m) corals and coralline algal assemblages developed continuously throughout both sites from 16 ka to ca. 8 ka, suggesting that coralgal assemblage variation ismore influenced by factors such as turbidity and water chemistry than sea-level rise alone.
    Keywords: 310-M0007A; 310-M0015A; 310-M0015B; 310-M0016A; 310-M0016B; 310-M0017A; 310-M0018A; AGE; Age, 14C AMS; Age, dated material; Age, error; Age, minimum/young; Age model; Age model calibration; Calcite; Description; DP Hunter; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Event label; Exp310; Integrated Ocean Drilling Program / International Ocean Discovery Program; IODP; Sample, optional label/labor no; Sample code/label; TAH-03A-1; TAH-03A-1A; TAH-03A-1B; TAH-03A-1C; TAH-03A-1D; TAH-03A-1E; TAH-03A-3; Tahiti, offshore Maraa; Tahiti Sea Level
    Type: Dataset
    Format: text/tab-separated-values, 133 data points
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  • 3
    Electronic Resource
    Electronic Resource
    Strategies for Amplification by Polymerase Chain Reaction of the Complete Sequence of the Gene Encoding Nuclear Large Subunit Ribosomal RNA in Corals (2000)
    Springer
    Marine biotechnology 2 (2000), S. 558-570 
    Details
    ISSN: 1436-2236
    Keywords: Key words: PCR, nuclear, large subunit ribosomal RNA gene, coral, Acropora.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract: The nearly complete nuclear large subunit ribosomal RNA (LSU rRNA) gene in corals was amplified by primers designed from polymerase chain reaction (PCR) strategies. The motif of the putative 3′-terminus of the LSU rRNA gene was sequenced and identified from intergenic spacer (IGS) clones obtained by PCR using universal primers designed for corals. The 3′-end primer was constructed in tandem with the universal 5′-end primer for the LSU rRNA gene. PCR fragments of 3500 bp were amplified for octocorals and non-Acropora scleractinian corals. More than 80% of the Acropora LSU rRNA gene (3000 bp) was successfully amplified by modification of the 5′-end of the IGS primer. Analysis of the 5′-end of LSU rDNA sequences, including the D1 and D2 divergent domains, indicates that the evolutionary rate of the LSU rDNA differs among these taxonomic groups of corals. The genus Acropora showed the highest divergence pattern in the LSU rRNA gene, and the presence of a long branch of the Acropora clade from the other scleractinian corals in the phylogenetic tree indicates that the evolutionary rate of Acropora LSU rDNA might have accelerated after divergence from the common ancestor of scleractinian corals.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s101260000040
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    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    The Togian Islands: coral reefs with a unique coral fauna and an hypothesised Tethys Sea signature (1999)
    Springer
    Coral reefs 18 (1999), S. 162-162 
    Details
    ISSN: 1432-0975
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s003380050173
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    Paper (German National Licenses)
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