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Reproductive ecology of three reef-forming, deep-sea corals in the New Zealand region

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Cold-Water Corals and Ecosystems

Part of the book series: Erlangen Earth Conference Series ((ERLANGEN))

Abstract

Reproductive ecology was examined in three deep-sea, reef-forming corals, Goniocorella dumosa, Solenosmilia variabilis and Enallopsammia rostrata from the ‘ Graveyard’ seamount complex on the Chatham Rise, New Zealand. Samples were collected from 890–1130 m depth in April 2001 using an epibenthic sled from the research vessel Tangaroa. S. variabilis was found to be gonochoric and this sexual trait was also suggested for E. rostrata and G. dumosa, although only colonies of one sex were collected. The likely mode of reproduction is broadcast spawning and fertilisation is likely to occur in late April or May coinciding with pelagic biomass accumulations at the end of summer. Reproductive development displayed a high level of synchrony among species and between seamount localities. E. rostrata was observed to contain both stage III and stage IV oocytes, indicating overlapping cohorts of oocyte growth, possibly related to food resources available. High fecundities were estimated for E. rostrata (>144 oocytes polyp−1), G. dumosa (>480 oocytes polyp−1) and S. variabilis (>290 oocytes polyp−1), with a negative correlation between oocyte size and number observed for all three species.

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References

  • Babcock RC, Bull G, Harrison PL, Heyward AJ, Oliver JK, Wallace CC, Willis BL (1986) Synchronous spawnings of 105 scleractinian coral species on the Great Barrier Reef. Mar Biol 90: 379–394

    Article  Google Scholar 

  • Babcock RC, Willis BL, Simpson CJ (1994) Mass spawning of corals on a high latitude coral reef. Coral Reefs 13: 161–169

    Article  Google Scholar 

  • Brooke S, Young CM (2003) Reproductive ecology of a deep-water scleractinian coral, Oculina varicosa from the southeast Florida shelf. Cont Shelf Res 23: 847–858

    Article  Google Scholar 

  • Cairns SD (1995) The marine fauna of New Zealand: Scleractinia (Cnidaria: Anthozoa). New Zealand Oceanogr Mem 103, 210 pp

    Google Scholar 

  • Clark M (1999) Fisheries for orange roughy (Hoplostethus atlantictus) on seamounts in New Zealand. Oceanol Acta 22: 593–602

    Article  Google Scholar 

  • Clark M, O’Shea S, Wood B, Wright I (2000) Seamount management: a report on seamounts potentially suitable for consideration under the Ministry of Fisheries seamount management strategy. NIWA Client Rep 00-33, 79 pp

    Google Scholar 

  • Fadlallah YH, Pearse JS (1982) Sexual reproduction in solitary corals: overlapping oogenic and brooding cycles, and benthic planulas in Balanophyllia elegans. Mar Biol 71: 223–231

    Google Scholar 

  • Frederiksen R, Jensen A, Westerberg H (1992) The distribution of the scleractinian coral Lophelia pertusa around the Faroe Islands and the relation to intertidal mixing. Sarsia 77: 157–171

    Google Scholar 

  • Freiwald A, Wilson JB (1998) Taphonomy of modern deep, cold-temperate water coral reefs. Hist Biol 13: 37–52

    Google Scholar 

  • Giese AC, Pearse JS (1974) Introduction: General principles. In: Giese AC, Pearse JS (eds) Reproduction of marine invertebrates. 1, Academic Press, New York, pp 1–49

    Google Scholar 

  • Harriott VJ (1983) Reproductive ecology of four scleractinian species at Lizard Island, Great Barrier Reef. Coral Reefs 2: 9–18

    Google Scholar 

  • Harrison PL, Wallace CC (1990) Reproduction, dispersal and recruitment of scleractinian corals. In: Dubinsky Z (ed) Coral Reefs. Elsevier, Amsterdam, pp 133–207

    Google Scholar 

  • Heath RA (1985) A review of the physical oceanography of the seas around New Zealand. New Zealand J Mar Fresh Res 19: 79–124

    Google Scholar 

  • Hessler RR, Sanders HL (1967) Faunal diversity in the deep-sea. Deep-Sea Res 14: 65–78

    Google Scholar 

  • Kojis BL, Quinn NJ (1981) Aspects of sexual reproduction and larval development in the shallow water hermatypic coral, Goniastrea australensis (Edwards and Haime, 1857). Bull Mar Sci 31: 558–573

    Google Scholar 

  • Koslow JA, Gowlett-Holmes K (1998) The seamount fauna off southern Tasmania: benthic communities, their conservation and impacts of trawling. Final Rep Environ Australia Fish Res Dev Corp, Australia

    Google Scholar 

  • Koslow JA, Gowlett-Holmes K, Lowry JK, O’Hara T, Poore GCB, Williams A (2001) Seamount benthic macrofauna off southern Tasmania: community structure and impacts of trawling. Mar Ecol Progr Ser 213: 111–125

    Google Scholar 

  • Mikkelsen N, Erlenkeuser H, Killingley JS, Berger WH (1982) Norwegian corals: radiocarbon and stable isotopes in Lophelia pertusa. Boreas 11: 163–171

    Google Scholar 

  • Mortensen PB (2001) Aquarium observations on the deep-water coral Lophelia pertusa (L. 1758) (Scleractinia) and selected associated invertebrates. Ophelia 54: 83–104

    Google Scholar 

  • Mortensen PB, Hovland M, Brattegard T, Farestveit R (1995) Deep-water bioherms of the scleractinian coral Lophelia pertusa (L.) at 64° N on the Norwegian shelf: structure and associated megafauna. Sarsia 80: 145–158

    Google Scholar 

  • Probert PK, McKnight DG, Grove SL (1997) Benthic invertebrate bycatch from a deep-water trawl fishery, Chatham Rise, New Zealand. Aquatic Conservation. Mar Fresh Ecosyst 7: 27–40

    Google Scholar 

  • Reed JK (1980) Distribution and structure of deep-water Oculina varicosa coral reefs off central eastern Florida. Bull Mar Sci 30: 667–677

    Google Scholar 

  • Richmond RH, Hunter CL (1990) Reproduction and recruitment of corals: comparisons among the Caribbean, the Tropical Pacific and the Red Sea. Mar Ecol Progr Ser 60: 185–203

    Google Scholar 

  • Rinkevich B, Loya Y (1979) The reproduction of the Red Sea Coral Stylophora pistillata. I. Gonads and Planulae. Mar Ecol Progr Ser 1: 133–144

    Google Scholar 

  • Rinkevich B, Loya Y (1987) Variability in the pattern of sexual reproduction of the coral Stylophora pistillata at Eilat, Red Sea: a long-term study. Biol Bull 173: 335–344

    Google Scholar 

  • Rogers AD (1999) The biology of Lophelia pertusa (L. 1758) and other deep-water reefforming corals and impacts from human activities. Int Rev Hydrobiol 84: 315–406

    Google Scholar 

  • Shlesinger Y, Goulet TL, Loya Y (1998) Reproductive patterns of scleractinian corals in the northern Red Sea. Mar Biol 132: 691–701

    Article  Google Scholar 

  • Sier CJS, Olive PW (1994) Reproduction and reproductive variability in the coral Pocillopora verrucosa from the Republic of Maldives. Mar Biol 118: 713–722

    Article  Google Scholar 

  • Squires DF (1964a) Biological results of the Chatham Islands 1954 expedition: Part 6: Scleractinia. New Zeal Dep Sci Indus Res Bull 139, 29 pp

    Google Scholar 

  • Squires DF (1964b) Fossil coral thickets in Wairarapa, New Zealand. J Paleont 38: 904–915

    Google Scholar 

  • Squires DF (1965) Deep-water coral structure on the Campbell Plateau, New Zealand. Deep-Sea Res 12: 785–788

    Google Scholar 

  • Stimson JS (1978) Mode and timing of reproduction in some common hermatypic corals of Hawaii and Enewetak. Mar Biol 48: 173–184

    Article  Google Scholar 

  • Szmant AM (1986) Reproductive ecology of Caribbean reef corals. Coral Reefs 5: 43–54

    Article  Google Scholar 

  • Tomascik T, Sander F (1987) Effects of eutrophication on reef-building corals II. Structure of scleractinian coral communities on fringing reefs, Barbados, West Indies. Mar Biol 94: 53–75

    Google Scholar 

  • Tranter PRG, Nicholson DN, Kinchington D (1982) A description of spawning and post-gastrula development of the cool temperate coral, Caryophyllia smithii. J Mar Biol Ass UK 62: 845–854

    Article  Google Scholar 

  • Waller RG, Tyler PA (in press) The reproductive ecology of two deep water, reef building scleractinians from the northeast Atlantic Ocean. Coral Reefs

    Google Scholar 

  • Waller RG, Tyler PA, Gage JD (2002) Reproductive ecology of the deep-sea scleractinian coral Fungiacyathus marenzelleri (Vaughan, 1906) in the northeast Atlantic Ocean. Coral Reefs 21: 325–331

    Google Scholar 

  • Wilson JB (1979) The distribution of the coral Lophelia pertusa (L.) [L. prolifera (Pallas)] in the northeast Atlantic. J Mar Biol Ass UK 59:149–164

    Google Scholar 

  • Wourms JP (1987) Oogenesis. In: Giese AC, Pearse JS (eds) Reproduction of marine invertebrates. 9. Blackwell, California, pp 49–178

    Google Scholar 

  • Wyrtki K (1962) The subsurface water masses in the Western South Pacific Ocean. Austral J Mar Fresh Res 13: 18–47

    Google Scholar 

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Burgess, S.N., Babcock, R.C. (2005). Reproductive ecology of three reef-forming, deep-sea corals in the New Zealand region. In: Freiwald, A., Roberts, J.M. (eds) Cold-Water Corals and Ecosystems. Erlangen Earth Conference Series. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-27673-4_36

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