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Epidemiology of skeletal eroding band on the Great Barrier Reef and the role of injury in the initiation of this widespread coral disease

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Abstract

Skeletal eroding band (SEB), which manifests as dense aggregations of the ciliate Halofolliculina corallasia, was the first coral disease described from the Indo-Pacific. Little is known about its etiology or impact. This study describes the distribution, prevalence and host range of SEB on a 500 km extent of the Great Barrier Reef (GBR), together with in situ rates of progression and infection following experimental injury. SEB occurred on 90–100% of reefs surveyed (n=18) in each of 3 years, demonstrating that SEB is widely distributed and persistent. SEB had the highest prevalence of any disease, affecting approximately 2% of 283,486 scleractinians and hydrocorals surveyed. Its host range was large, affecting 12 families and at least 82 scleractinian species, as well as the hydrocoral, Millepora. Corals in the families Pocilloporidae and Acroporidae were most susceptible, the former being up to five times more susceptible than other families. Progressive tissue loss was recorded on 95% of Acropora muricata colonies monitored (n = 18), with rates of SEB progression averaging ∼2 mm/day. Injury experiments demonstrated that H. corallasia, the putative pathogen of SEB, readily colonised recently exposed coral skeleton in the absence of a vector, but did not colonise intact coral tissue. Invading ciliates failed to form band-like aggregations associated with progressive tissue loss on any of three coral species tested experimentally, suggesting that, while H. corallasia readily colonises recently exposed coral skeleton, it may not be sufficient in itself to cause tissue mortality. Interactions with additional agents or factors, increasing ciliate virulence or lowering disease resistance of coral hosts may be required before halofolliculinid infections become associated with tissue loss.

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References

  • Andrews EA (1914) Distribution of folliculina in 1914. Biol Bull 29:373–380

    Article  Google Scholar 

  • Andrews EA (1923) Folliculina: case making, anatomy and transformation. J Morphol 38:207–278

    Article  Google Scholar 

  • Antonius A (1981) Coral reef pathobiology: a review. Proc 4th Int Coral Reef Symp 2:3–6

    Google Scholar 

  • Antonius A (1985) Black band disease infection experiments on hexacorals and octocorals. Proc 5th Int Coral Reef Congr 6:155–160

    Google Scholar 

  • Antonius A (1999) Halofolliculina corallasia, a new coral killing ciliate on Indo-Pacific reefs. Coral Reefs 18:300

    Article  Google Scholar 

  • Antonius A, Riegl B (1997) A possible link between coral disease and a corallivorous snail (Drupella cornus) outbreak in the Red Sea. Atoll Res Bull 47:1–9

    Google Scholar 

  • Antonius A, Riegl B (1998) Coral diseases and Drupella cornus invasion in the Red Sea. Coral Reefs 17:48

    Article  Google Scholar 

  • Antonius A, Lipscomb D (2001) First protozoan coral-killer identified in the Indo-Pacific. Atoll Res Bull 481–493:1–21

    Google Scholar 

  • Bak RPM, Criens SR (1981) Survival after fragmentation of colonies of Madacis mirabilis, Acropora palmata and A.cervicornis (Scleractinia) and the subsequent impact of a coral disease. Proc 4th Int Coral Reef Symp 2:221–227

    Google Scholar 

  • Boyett H, Bourne D, Willis BL (2007) Elevated temperatures and light enhance progression and spread of black band disease on staghorn corals of the Great Barrier Reef. Mar Biol 151:1711–1720

    Article  Google Scholar 

  • Bruckner AW (2002) Priorities for effective management of coral diseases. NOAA Technical Memorandum. NMFS-OPR-22. NOAA National Marine Fisheries Service, Silver Springs

  • Cervino J, Goreau T, Nagelkerken I, Smith GW, Hayes R (2001) Yellow band and dark spot syndromes in Caribbean coral: distribution, rate of spread, cytology, and the effects on abundance and division rate of zooxanthellae. Hydrobiologia 460:53–63

    Article  Google Scholar 

  • Cróquer A, Bastidas C, Lipscomb D (2006a) Folliculinid ciliates: a new threat to Caribbean corals? Dis Aquat Org 69:75–78

    Article  PubMed  Google Scholar 

  • Cróquer A, Bastidas C, Lipscomp D, Rodríguez-Martínez RE, Jordan-Dahlgren E, Guzman HM (2006b) First report of folliculinid ciliates affecting Caribbean scleractinian corals. Coral Reefs 25:187–191

    Article  Google Scholar 

  • Cummings RL (1999) Predation on reef-building corals: multiscale variation in the density of three corallivorous gastropods, Drupella spp. Coral Reefs 18:147–157

    Article  Google Scholar 

  • Dalton SJ, Smith SDA (2006) Coral disease dynamics at a subtropic location, Solitary Islands Marine Park, Eastern Australia. Coral Reefs 25:37–45

    Article  Google Scholar 

  • De’ath G, Moran PJ (1998) Factors affecting the behaviour of crown-of-thorns starfish (Acanthaster planci L.) on the Great Barrier Reef. 2 Feeding preferences. J Exp Mar Biol Ecol 220:107–126

    Article  Google Scholar 

  • Fine M, Oren U, Loya Y (2002) Bleaching effect on regeneration and resource translocation in the coral Oculina patagonica. Mar Ecol Prog Ser 234:119–125

    Article  Google Scholar 

  • Garzon-Ferreira J, Zea S (1992) A mass mortality of Gorgonia ventalina (Cnidaria: Gorgoniidae) in the Santa Marta area, Caribbean coast of Columbia. Bull Mar Sci 50:522–526

    Google Scholar 

  • Green E, Bruckner A (2000) The significance of coral disease epizootiology for coral reef conservation. Biol Conserv 96:347–361

    Article  Google Scholar 

  • Grottoli AG, Rodrigues LJ, Juarez C (2004) Lipids and stable carbon isotopes in two species of Hawaiian corals, Porites compressa and Montipora verrusosa, following a bleaching event. Mar Biol 145:621–631

    Article  CAS  Google Scholar 

  • Guzman HM, Cortes J (1984) Mortandad de Gorgonia flabellum Linnaeus (Octocorallia:Gorgoniidae) en la costa Caribe de Costa Rica. Rev Biol Trop 32:305–308

    Google Scholar 

  • Hall V (1997) Effects of injury on growth, reproduction and survivorship for common reef-crest corals. Proc 8th Int Coral Reef Symp 1:571–574

    Google Scholar 

  • Harvell CD, Jordan-Dahlgren E, Merkel SM, Rosenberg E, Raymundo LJ, Smith G, Weil E, Willis BL (2007) Coral disease, environmental drivers and the balance between coral and microbial associates. Oceanography 20:36–59

    Google Scholar 

  • Harvell CD, Kim K, Burkholder J, Colwell RR, Epstein PR, Grimes J, Hofmann EE, Lipp EK, Osterhaus ADME, Overstreet R, Porter JW, Smith GW, Vasta GR (1999) Emerging marine diseases—climate links and anthropogenic factors. Science 285:1505–1510

    Article  PubMed  CAS  Google Scholar 

  • Kim K, Harvell CD (2004) The rise and fall of a six year coral-fungal epizootic. Am Nat 164:S52–S63

    Article  PubMed  Google Scholar 

  • Loya Y (2004) Coral reefs of Eliat: past, present and future. In: Rosenberg E, Loya Y (eds) Coral disease and health. Springer, Berlin, pp 1–34

    Google Scholar 

  • Marshall PA (2000) Skeletal damage in reef corals: relating resistance to colony morphology. Mar Ecol Prog Ser 200:177–189

    Article  Google Scholar 

  • McClanahan TR, McLaughlin SM, Davy JE, Wilson WH, Peters EC, Price KL, Maina J (2004) Observations of a new source of coral mortality along the Kenyan coast. Hydrobiologia 530:469–479

    Article  Google Scholar 

  • McCullagh P, Nelder JA (1989) Generalized linear models. Chapman Hall, London

    Google Scholar 

  • Meesters EH, Bak RPM (1993) Effects of coral bleaching on tissue regeneration potential and coral survival. Mar Ecol Prog Ser 96:189–198

    Article  Google Scholar 

  • Miller J, Waara R, Muller E, Rogers C (2006) Coral bleaching and disease combine to cause extensive mortality on reefs in US Virgin Islands. Coral Reefs 25:418

    Article  Google Scholar 

  • Nagelkerken I, Buchan K, Smith G, Boniar K, Bush P, Garzon-Ferreira J, Botero L, Gayle P, Heberer C, Petrovic C, Pors L, Yoshioka P (1997) Widespread disease in Caribbean Sea Fans: I Spreading and general characteristics. Proc 8th Int Coral Reef Symp 1:679–682

    Google Scholar 

  • Page CA, Willis BL (2006) Distribution, host range and large-scale variability in the prevalence of black band disease on the Great Barrier Reef, Australia. Dis Aquat Org 69:41–51

    Article  PubMed  Google Scholar 

  • Patterson KL, Porter JW, Ritchie KB, Polson SW, Mueller E, Peters EC, Santavy DL, Smith GW (2002) The etiology of white pox, a lethal disease of the Caribbean elkhorn coral, Acropora palmata. Proc Natl Acad Sci USA 99:8725–8730

    Article  PubMed  CAS  Google Scholar 

  • Porter J, Dustan P, Jaap W, Patterson KL, Kosmynin V, Meier O, Patterson M, Parsons M (2001) Patterns of spread of coral disease in the Florida Keys. Hydrobiologia 460:1–24

    Article  Google Scholar 

  • Pratchett MS (2007) Feeding preferences of Acanthaster planci (Echinodermata: Asteroidea) under controlled conditions of food availability. Pac Sci 61:113–120

    Article  Google Scholar 

  • Precht WF, Bruckner AW, Aronson RB, Bruckner RJ (2002) Endangered acroporid corals of the Caribbean. Coral Reefs 21:41–42

    Google Scholar 

  • Raymundo LJ, Rosell KB, Reboton CT, Kaczmarsky L (2005) Coral disease on Philippine reefs: genus Porites is a dominant host. Dis Aquat Org 64:181–191

    Article  PubMed  Google Scholar 

  • Raymundo LJH, Harvell CD, Reynolds TL (2003) Porites ulcerative white spot disease: description, prevalence, and host range of a new coral disease affecting Indo-Pacific reefs. Dis Aquat Org 56:95–104

    Article  PubMed  Google Scholar 

  • Riegl B, Antonius A (2003) Halofolliculina skeleton eroding band (SEB): a coral disease with fossilization potential? Coral Reefs 22:48

    Article  Google Scholar 

  • Ritchie KB (2006) Regulation of microbial populations by coral surface mucus and mucus-associated bacteria. Mar Ecol Prog Ser 322:1–14

    Article  CAS  Google Scholar 

  • Roff G, Hoegh-Guldberg O, Fine M (2006) Intra-colonial response to Acroporid “white syndrome” lesions in tabular Acropora spp. (Scleractinia). Coral Reefs 25:255–264

    Article  Google Scholar 

  • Sutherland KP, Porter JW, Torres C (2004) Disease and immunity in Caribbean and Indo-Pacific zooxanthellate corals. Mar Ecol Prog Ser 266:273–302

    Article  Google Scholar 

  • Wallace CC (1985) Reproduction, recruitment and fragmentation in nine sympatric species of the coral Acropora. Mar Biol 88:217–233

    Article  Google Scholar 

  • Ward JR, Lafferty KD (2004) The elusive baseline of marine disease: are diseases in ocean ecosystems increasing? PLoS Biology 2:542–547

    CAS  Google Scholar 

  • Weil E (2004) Coral reef disease in the wider Caribbean: status and prognosis. In: Rosenberg E, Loya Y (eds) Coral disease and health. Springer, Berlin, pp 35–64

    Google Scholar 

  • Weil E, Smith G, Gil-Agudelo DL (2006) Status and progress in coral reef disease research. Dis Aquat Org 69:1–7

    Article  PubMed  Google Scholar 

  • Williams Jr EH, Bartels PJ, Bunkley-Williams L (1999) Predicted disappearance of coral-reef ramparts: a direct result of major ecological disturbances. Global Change Biol 5:839–845

    Article  Google Scholar 

  • Willis BL, Page CA, Dinsdale EA (2004) Coral disease on the Great Barrier Reef. In: Rosenberg E, Loya Y (eds) Coral disease and health. Springer, Berlin, pp 69–104

    Google Scholar 

  • Winkler R, Antonius A, Abigail Renegar D (2004) The skeleton eroding band disease on coral reefs of Aqaba, Red Sea. PSZNI Mar Ecol 25:129–144

    Article  Google Scholar 

  • Wobeser GA (2006) Essentials of disease in wild animals. Blackwell, Ames

    Google Scholar 

Download references

Acknowledgments

We thank S. Neale, D. Thomson, D. Bourne, S. Anthony, M. Sussman, L. Anderson, M. Fraser, the crew of the RV Lady Basten, L. Vail, A. Hoggett, L. Pearce, P. Venables, G. Coleman, C. Syms, P. Munday, M. McCormick, S. Kininmonth and D. Lipscomb for their help and assistance. This research was funded by the ARC Centre of Excellence for Coral Reef Studies, the Coral Disease Working Group of the GEF CRTR Program, the 2004 Lizard Island Fellowship, James Cook University, and a Great Barrier Reef Marine Park Authority Science for Management Award. Townsville sector fieldwork was supported by the Australian Institute of Marine Science. Comments by two anonymous reviewers improved this manuscript.

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Correspondence to C. A. Page.

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Communicated by Geology Editor B. Riegl.

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Page, C.A., Willis, B.L. Epidemiology of skeletal eroding band on the Great Barrier Reef and the role of injury in the initiation of this widespread coral disease. Coral Reefs 27, 257–272 (2008). https://doi.org/10.1007/s00338-007-0317-8

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  • DOI: https://doi.org/10.1007/s00338-007-0317-8

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