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Neosiphonia howei (Ceramiales: Rhodomelaceae)—a common epiphyte of the spreading coral reef alga Lobophora variegata (Dictyotales: Dictyotaceae)

Published online by Cambridge University Press:  12 February 2013

Anna Fricke ,
Tamara V. Titlyanova ,
Maggy M. Nugues  and
Kai Bischof
Anna Fricke*
Affiliation:
Leibniz Center for Tropical Marine Ecology (ZMT), Fahrenheitstrasse 6, 28359 Bremen, Germany University of Bremen, Department of Marine Botany, Leobener Strasse NW2, 28359 Bremen, Germany
Tamara V. Titlyanova
Affiliation:
A.V. Zhirmunsky Institute of Marine Biology, Far Eastern Branch of the Russian Academy of Sciences, Palchevskogo 17, Vladivostok, 690041, Russia
Maggy M. Nugues
Affiliation:
USR 3278 CRIOBE CNRS-EPHE and Laboratoire d'Excellence 'CORAIL', Centre de Biologie et d'Ecologie Tropicale et Méditerranéenne, Université de Perpignan, 66860 Perpignan Cedex, France CARMABI Foundation, Piscaderabaai z/n, PO Box 2090, Willemstad, Curaçao, Netherlands Antilles
Kai Bischof
Affiliation:
University of Bremen, Department of Marine Botany, Leobener Strasse NW2, 28359 Bremen, Germany
*
Correspondence should be addressed to: A. Fricke, University of Bremen, Department of Marine Botany, Leobener Strasse NW2, 28359 Bremen, Germany email: [email protected]
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Abstract

Fleshy macroalgae are becoming a dominant benthic component on Caribbean coral reefs, with increased abundance and frequency across all reef zones. Over the past two decades, the brown alga Lobophora variegata has proliferated on shallow and deep reefs in Curaçao, former Netherlands Antilles. This alga provides a living substrate for a diverse epiphytic community. Here we report on Neosiphonia howei (Rhodomelaceae: Ceramiales), growing epiphytically on L. variegata over a broad depth gradient (6.5 to 40 m). Although N. howei has been reported as a typical epiphyte in shallow water, it was commonly found on L. variegata blades on the reef slope in all fertile stages. This epiphyte anchored deeply into the host tissue, suggesting hemiparasitic behaviour. The spread of L. variegata may have increased the depth-range of N. howei and the exact nature of the interaction between N. howei and its host deserves further research considering the importance of fleshy macroalgae on coral reefs.

Keywords

deep coral reefCuraçaophase shiftsturf algae
Type
Research Article
Information
Marine Biodiversity Records , Volume 6 , 2013 , e3
Copyright
Copyright © Marine Biological Association of the United Kingdom 2013

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References

REFERENCES

Abbott, I.A. (1999) Marine red algae of the Hawaiian Islands. Hawaii, Honolulu: Bishop Museum Press.Google Scholar
Ballantine, D.L. (1979) The distribution of algal epiphytes on macrophyte hosts offshore from La Parguera, Puerto Rico. Botanica Marina 22, 107–110.Google Scholar
Bak, R.P.M. (1976) The growth of coral colonies and the importance of crustose coralline algae and burrowing sponges in relation with carbonate accumulation. Netherlands Journal of Sea Research 10, 285–337.Google Scholar
Birrell, C.L., McCook, L.J., Willis, B.L. and Diaz-Pulido, G.A. (2008) Effects of benthic algae on the replenishment of corals and the implications for the resilience of coral reefs. Oceanography and Marine Biology: an Annual Review 46, 25–63.Google Scholar
Burke, L. and Maidens, J. (2004) Reefs at risk in the Caribbean. Washington, DC: World Resources Institute, 81 pp.Google Scholar
Cattaneo, A. (1983) Grazing on epiphytes. Limnology and Oceanography 28, 124–132.Google Scholar
Dawes, C.J. and Mathieson, A.C. (2008) The seaweeds of Florida. Gainesville, FL: University Press of Florida, 656 pp.Google Scholar
Ducker, S.C. and Knox, R.B. (1984) Epiphytism at the cellular level with special reference to algal epiphytes. Encyclopedia of Plant Physiology 17, 113–130.Google Scholar
Fong, P. and Paul, V.J. (2011) Coral reef algae. In Dubinsky, Z. and Stambler, N. (eds) Coral reefs: an ecosystem in transition. Dordrecht, The Netherlands: Springer, pp. 241–272 Google Scholar
Foster, N.L., Box, S.J. and Mumby, P.J. (2008) Competitive effects of macroalgae on the fecundity of the reef-building coral Montastraea annularis. Marine Ecology Progress Series 367, 143–152.Google Scholar
Frankovich, T. and Zieman, J. (2005) A temporal investigation of grazer dynamics, nutrients, seagrass leaf productivity, and epiphyte standing stock. Estuaries and Coasts 28, 41–52.Google Scholar
Fricke, A., Teichberg, M., Beilfuss, S. and Bischof, K. (2011a) Succession patterns in algal turf vegetation on a Caribbean coral reef. Botanica Marina 54, 111–126.Google Scholar
Fricke, A., Titlyanova, T., Nugues, M.M. and Bischof, K. (2011b) Depth-related variation in epiphytic communities growing on the brown alga Lobophora variegata in a Caribbean coral reef. Coral Reefs 30, 967–973.Google Scholar
Garbary, D. and Deckert, R. (2004) Three part harmony—Ascophyllum and its symbionts. Symbiosis 4, 309–321.Google Scholar
Hall, M.O. and Bell, S.S. (1988) Response of small motile epifauna to complexity of epiphytic algae on seagrass blades. Journal of Marine Research 46, 613–630.Google Scholar
Hollenberg, G.J. (1968) An account of species of red aga Polysiphonia of central and western tropical Pacific Ocean. 2. Polysiphonia . Pacific Science 22, 198–207.Google Scholar
Holmström, C. and Kjelleberg, S. (2000) Bacterial interactions with marine fouling organisms. In Evans, L.E. (ed.) Biofilms: recent advances in their study and control. Boca Raton, FL: CRC Press, pp. 101–115.Google Scholar
Hughes, T.P., Rodrigues, M.J., Bellwood, D.R., Ceccarelli, D., Hoegh-Guldberg, O., McCook, L., Moltschaniwskyj, N., Pratchett, M.S., Steneck, R.S. and Willis, B. (2007) Phase shifts, herbivory, and the resilience of coral reefs to climate change. Current Biology 17, 360–365.Google Scholar
Jiang, Z.D., Jensen, P.R. and Fenical, W. (1999) Lobophorins A and B, new antiinflammatory macrolides produced by a tropical marine bacterium. Bioorganic & Medicinal Chemistry Letters 9, 2003–2006.Google Scholar
Jompa, J. and McCook, L.J. (2003) Coral–algal competition: macroalgae with different properties have different effects on corals. Marine Ecology Progress Series 258, 87–95.Google Scholar
Kuffner, I.B. and Paul, V.J. (2004) Effects of the benthic cyanobacterium Lyngbya majuscula on larval recruitment of the reef corals Acropora surculosa and Pocillopora damicornis . Coral Reefs 23, 455–458.Google Scholar
Littler, M.M. and Littler, D.S. (2000) Caribbean reef plants. Washington, DC: OffShore Graphics, Inc. Google Scholar
Loureiro, R., Reis, R. and Critchley, A. (2010) In vitro cultivation of three Kappaphycus alvarezii (Rhodophyta, Areschougiaceae) variants (green, red and brown) exposed to a commercial extract of the brown alga Ascophyllum nodosum (Fucaceae, Ochrophyta). Journal of Applied Phycology 22, 101–104.Google Scholar
Michael, T.S., Shin, H.W., Hanna, R. and Spafford, D.C. (2008) A review of epiphyte community development: surface interactions and settlement on seagrass. Journal of Environmental Biology 29, 629–638.Google Scholar
Mumby, P.J., Foster, N.L. and Fahy, E.A.G. (2005) Patch dynamics of coral reef macroalgae under chronic and acute disturbance. Coral Reefs 24, 681–692.Google Scholar
Mumby, P.J., Hastings, A. and Edwards, H.J. (2007) Thresholds and the resilience of Caribbean coral reefs. Nature 450, 98–101.Google Scholar
Nugues, M.M. and Bak, R.P.M. (2008) Long-term dynamics of the brown macroalga Lobophora variegata on deep reefs in Curaçao. Coral Reefs 27, 389–393.Google Scholar
Rao, D., Webb, J.S. and Kjelleberg, S. (2006) Microbial colonization and competition on the marine alga Ulva australis . Applied and Environmental Microbiology 72, 5547–5555.Google Scholar
Sokal, R.R. and Rohlf, F.J. (1995) Biometry: the principles and practice of statistics in biological research. 3rd edition. New York: W.H. Freeman.Google Scholar
Taylor, W.R. (1945) Pacific marine algae of the Allan Hancock Expeditions to the Galapagos Islands. Allan Hancock Pacific Expeditions 12, i–iv, 1–528 Google Scholar
Titlyanov, E.A., Yakovleva, I.M. and Titlyanova, T.V. (2007) Interaction between benthic algae (Lyngbya bouillonii, Dictyota dichotoma) and scleractinian coral Porites lutea in direct contact. Journal of Experimental Marine Biology and Ecology 342, 282–291.Google Scholar
Tobler, F. (1906) Zur Biologie der Epiphyten im Meere. Deutsche Botanische Gesellschaft 24, 552 pp.Google Scholar
Van den Hoek, C., Colijn, F., Cortel-Breeman, A.M. and Wanders, J.B.W. (1972) Algal vegetation-types along the shores of inner bays and lagoons of Curaçao and of the lagoon Lac (Bonaire), Netherlands Antilles. Verhandelingen Koningklijke Nederlandse Akademie van Wetenschap, Afdeling Natuurkunde 61, 1–72.Google Scholar
Vairappan, C., Chung, C., Hurtado, A., Soya, F., Lhonneur, G. and Critchley, A. (2008) Distribution and symptoms of epiphyte infection in major carrageenophyte-producing farms. Journal of Applied Phycology 20, 477–483.Google Scholar
Van Duyl, F.C. (1985) Atlas of living reefs of Curaçao and Bonaire (Netherlands Antilles). Foundation for Scientific Research in Surinam and the Netherlands Antilles, Utrecht, No. 117, 37 pp.Google Scholar