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Type: Articles
Published: 2012-06-15
Page range: 24–39
Abstract views: 32
PDF downloaded: 15

Discovery of Aphanipathes verticillata (Cnidaria: Anthozoa: Antipatharia) in the Hawaiian Islands

National Museum of Natural History, Smithsonian Institution, Washington, DC, USA
Papahānaumokuākea Marine National Monument, 6600 Kalaniana'ole Hwy, Suite 300, Honolulu, HI 96825
U.S. Fish and Wildlife Service, Pacific Islands Fish and Wildlife Office, 300 Ala Moana Boulevard, Room 3-122, Honolulu, HI 96850
Sackler Institute for Comparative Genomics, Division of Invertebrate Zoology, American Museum of Natural History, New York, NY, USA
Coelenterata Aphanipathidae Aphanipathes verticillata mauiensis new subspecies black coral range extension

Abstract

Mesophotic coral reef surveys conducted off Maui in 2008–2009 revealed several specimens superficially resembling thecommercial black coral species Antipathes griggi Opresko 2009. After subsequent microscopic examination of the skel-etal features, these colonies proved to be morphologically very similar to Aphanipathes verticillata Brook 1889, a speciesnever before reported from the Hawaiian Islands. A comparison with samples of the type material of A. verticillata indi-cated that the specimens collected in Hawaiian waters differed from the type in having simplier and less dense tubercleson the skeletal spines, a character which merits the recognition of the Hawaiian population as a new subspecies, A. ver-ticillata mauiensis. Colonies of the new subspecies exhibit considerable morphological variation; DNA analysis of fifteenspecimens ruled out the possibility of the presence of a cryptic species. Further DNA investigations on specimens fromvarious localities in the western Pacific and Indian Ocean are needed to better understand the genetic relationship betweenthe two forms. The morphological similarity of A. verticillata mauiensis with Antipathes griggi raises questions concern-ing the validity of past field surveys evaluating the population size and structure of A. griggi since it is possible that thetwo species could easily be misidentified based on gross morphology alone. Additional studies are also needed to document the geographic and bathymetric distribution of the subspecies along the Hawaiian Island chain.

References

  1. Andolfatto, P. (2005) Adaptive evolution of non-coding DNA in Drosophila. Nature, 437, 1149–1152.

    Brook, G. (1889) Report on the Antipatharia. Reports of the Scientific Research Voyage of the H.M.S. Challenger, Zoology, 32(80), 1–222, pls 1–15.

    Brugler, M.R. (2011) Molecular evolution in black corals (Cnidaria: Anthozoa: Hexacorallia): Implications for antipatharian systematics. Ph.D. Dissertation, University of Louisiana at Lafayette.

    Chen, C., Chiou, C.Y., Dai, C.F. & Chen, C.A. (2008a) Unique mitogenomic features in the scleractinian family Pocilloporidae (Scleractinia; Astrocoeniina). Marine Biotechnology, 10, 538–553.

    Chen, C., Dai, C-F., Plathong, S., Chiou, C-Y. & Chen, C.A. (2008b) The complete mitochondrial genomes of needle corals, Seriatopora spp. (Scleractinia: Pocilloporidae): An idiosyncratic atp8, duplicated trnW gene and hypervariable regions used to determine species phylogenies and recently diverged populations. Molecular Phylogenetics and Evolution, 46, 19–33.

    Forsman, Z.H., Barshis, D.J., Hunter, C.L. & Toonen, R.J. (2009) Shape-shifting corals: molecular markers show morphology is evolutionarily plastic in Porites. BMC Evolutionary Biology, 9, 45.

    France, S.C., Rosel, P.E., Agenbroad, J.E., Mullineaux, L.S. & Kocher, T.D. (1996) DNA sequence variation of mitochondrial large-subunit rRNA provides support for a two-subclass organization of the Anthozoa (Cnidaria). Molecular Marine Biology and Biotechnology, 5, 15–28.

    Gray, J.E. (1857) Synopsis of the families and genera of axiferous zoophytes or barked corals. Proceedings of the Zoological Society of London, 25, 278–294, pl. 9.

    Grigg, R.W. (2001) Black coral: history of a sustainable fishery in Hawai‘i. Pacific Science, 55(3), 291–299.

    Grigg, R.W. (2002) Precious corals in Hawai‘i: discovery of a new bed and revised management measures for existing beds. Marine Fisheries Review, 64(1), 13–20.

    Hebert, P.D.N., Cywinska, A., Ball, S.L. & deWaard, J.R. (2003) Biological identifications through DNA barcodes. Proceedings of the Royal Society, B 270, 313–321.

    Hellberg, M.E. (2006) No variation and low synonymous substitution rates in coral mtDNA despite high nuclear variation. BMC Evolutionary Biology, 6, 24.

    McFadden, C.S., Benayahu, Y., Pante, E., Thoma, J.N. Nevarez, P.A. & France, S.C. (2010) Limitations of mitochondrial gene barcoding in Octocorallia. Molecular Ecology Resources, 11, 19–31.

    McKnight, M.L. & Shaffer, H.B. (1997) Large, rapidly evolving intergenic spacers in the mitochondrial DNA of the salamander family Ambystomatidae (Amphibia: Caudata). Molecular Biology and Evolution, 14, 1167–1176.

    Miller, K.J. (1996) Piecing together the reproductive habits of New Zealand’s endemic black corals. Water and Atmosphere, 4, 18–19.

    Opresko, D.M. (1972) Redescriptions and reevaluations of the antipatharians described by L.D. de Pourtales. Bulletin of Marine Science, 22(4), 950–1017.

    Opresko, D.M. (1974) A study of the classification of the Antipatharia (Coelenterata:Anthozoa) with redescriptions of eleven species. Ph.D. Dissertation, University of Miami, Miami, FL, 193 pp.

    Opresko, D.M. (2004) Revision of the Antipatharia (Cnidaria: Anthozoa). Part IV. Establishment of a new family, Aphanipathidae. Zoologische Mededelingen, Leiden, 78, 209–240.

    Opresko, D.M. (2009) A new name for the Hawaiian antipatharian coral formerly known as Antipathes dichotoma (Cnidaria: Anthozoa: Antipatharia). Pacific Science, 63, 277–291.

    Pallas, P.S. (1766) Elenchus Zoophytorum Sistens Generum Adumbrationes Generaliores et Specierum Cognitarum Succinctas Descriptiones cum SelectisAuctorum Synonymis, Hagae-Comitum, 451 pp.

    Pesch, A.J. van (1914) The Antipatharia of the Siboga Expedition. Siboga-Expeditie Monographe, 17, 1–258, pls 1–8.

    Pourtalès, L.F. de (1880) Zoological results of the Blake expedition to the Caribbean Sea. Bulletin of the Museum of Comparative Zoology, Harvard, 6(4), 113–118.

    Schultze, L. S. (1902) Die Antipatharien der Deutschen Tiefsee-Expedition, 1898–1899. Wissenschaftliche Ergebnisse der deutschen Tiefsee-Expedition auf dem Dampfer Valdivia, 3, 90–100.

    Shearer, T.L., van Oppen, M.J.H, Romano, S.L. & Worheide, G. (2002) Slow mitochondrial DNA sequence evolution in the Anthozoa (Cnidaria). Molecular Ecology, 11, 2475–2487.

    Thoma, J.N., Pante, E., Brugler, M.R. & France, S.C. (2009) Deep-sea octocorals and antipatharians show no evidence of seamount-scale endemism in the NW Atlantic. Marine Ecology Progress Series, 397, 25–35.

    Verrill, A.E. (1928) Hawaiian shallow-water Anthozoa. Bulletin of the Bishop Museum, 49, 1–30.

    Wagner, D., Brugler, M.R., Opresko, D.M., France, S.C., Montgomery, A.D. & Toonen, R.J. (2010) Using morphometrics, in situ observations and genetic characters to distinguish among commercially valuable Hawaiian black coral species; a redescription of Antipathes grandis Verrill, 1928 (Antipatharia: Antipathidae). Invertebrate Systematics, 24, 271–290.

    Wei N-W.V., Wallace C.C., Dai C-F., Pillay K.R.M. & Chen C.A. (2006) Analyses of the ribosomal internal transcribed spacers (ITS) and the 5.8S gene indicate that extremely high rDNA heterogeneity is a unique feature in the scleractinian coral genus Acropora (Scleractinia; Acroporidae). Zoological Studies, 45, 404–418.