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Advances in the aquatic sciences
RESEARCH ARTICLE

Determining background levels and defining outbreaks of crustose coralline algae disease on the Great Barrier Reef

I. R. Miller A B , M. Logan A , K. A. Johns A , M. J. Jonker A , K. Osborne A and H. P. A. Sweatman A
+ Author Affiliations
- Author Affiliations

A Australian Institute of Marine Science, PMB#3 Townsville MC, Qld 4810, Australia.

B Corresponding author. Email: i.miller@aims.gov.au

Marine and Freshwater Research 64(11) 1022-1028 https://doi.org/10.1071/MF12330
Submitted: 22 November 2012  Accepted: 26 April 2013   Published: 19 July 2013

Abstract

Crustose coralline algae (CCA) play a vital role in coral-reef ecosystems and, like other marine organisms, they are vulnerable to disease. Between 2006 and 2011, incidence of two types of CCA disease was systematically recorded over a large portion of the Great Barrier Reef (GBR). The two CCA diseases that were recorded, coralline lethal orange disease and coralline white-band syndrome, were ubiquitous on the GBR, but generally at low levels comparable to those found on reefs in other parts of the Indo-Pacific. The present broad-scale study of the distribution and abundance of CCA disease on the GBR provides information on background levels of these diseases and allows regional thresholds for outbreaks to be defined. This will allow managers and researchers to focus attention on areas of high incidence of CCA disease to increase our understanding of causes and the environmental impacts of CCA disease at a time when coral reefs are under growing anthropogenic threats.

Additional keywords: coralline, disease, outbreak.


References

Adey, W. (1978). Coral reef morphogenesis: a multidimensional model. Science 202, 831–837.
Coral reef morphogenesis: a multidimensional model.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3cvisVertA%3D%3D&md5=5ed43c262d12caf0ec3a6adf52d404f2CAS | 17752443PubMed |

Adey, W. H. (1998). Coral reefs: algal structured and mediated ecosystems in shallow, turbulent, alkaline waters. Journal of Phycology 34, 393–406.
Coral reefs: algal structured and mediated ecosystems in shallow, turbulent, alkaline waters.Crossref | GoogleScholarGoogle Scholar |

Aeby, G., Work, T., Fenner, D., and Didonato, E. (2009). Coral and crustose coralline algae disease on the reefs of American Samoa. In ‘Proceedings of the 11th International Coral Reef Symposium, Fort Lauderdale, 7–11 July 2008’. (Eds B. M. Riegl and R. E. Dodge.) Volume 1, Session number 7. pp. 200–204. (National Coral Reef Initiative, Nova South Eastern University, Florida.)

Anthony, K. R. N., Kline, D. I., Diaz-Pulido, G., Dove, S., and Hoegh-Guldberg, O. (2008). Ocean acidification causes bleaching and productivity loss in coral reef builders. Proceedings of the National Academy of Sciences, USA 105, 17442–17446.
Ocean acidification causes bleaching and productivity loss in coral reef builders.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhsVWns7jM&md5=8d89a576786795d30fdcb9c8ab4afe81CAS |

Aronson, R. B., and Precht, W. F. (2001). White-band disease and the changing face of Caribbean coral reefs. Hydrobiologia 460, 25–38.
White-band disease and the changing face of Caribbean coral reefs.Crossref | GoogleScholarGoogle Scholar |

Ballantine, D., Weil, E., and Ruiz, H. (2005). Coralline white band syndrome, a coralline algal affliction in the tropical Atlantic. Coral Reefs 24, 117.
Coralline white band syndrome, a coralline algal affliction in the tropical Atlantic.Crossref | GoogleScholarGoogle Scholar |

Bolker, B. M., Brooks, M. E., Clark, C. J., Geange, S. W., Poulsen, J. R., Stevens, M. H. H., and White, J.-S. S. (2009). Generalized linear mixed models: a practical guide for ecology and evolution. Trends in Ecology & Evolution 24, 127–135.
Generalized linear mixed models: a practical guide for ecology and evolution.Crossref | GoogleScholarGoogle Scholar |

Bruno, J. F., Selig, E. R., Casey, K. S., Page, C. A., Willis, B. L., Harvell, C. D., Sweatman, H., and Melendy, A. M. (2007). Thermal stress and coral cover as drivers of coral disease outbreaks. PLoS Biology 5, e124.
Thermal stress and coral cover as drivers of coral disease outbreaks.Crossref | GoogleScholarGoogle Scholar | 17488183PubMed |

Carpenter, R. C. (1990). Mass mortality of Diadema antillarum. I. Long-term effects on sea urchin population-dynamics and coral reef algal communities. Marine Biology 104, 67–77.
Mass mortality of Diadema antillarum. I. Long-term effects on sea urchin population-dynamics and coral reef algal communities.Crossref | GoogleScholarGoogle Scholar |

Cervino, J. M., Littler, M. M., Littler, D. S., Polson, S., Goreau, T. J, Brooks, B., and Smith, G. W. (2005). Identification of microbes associated with coralline lethal algal disease and its relationship to glacial ice melt (global warming). Phytopathology 95, 120–121.

Chisholm, J. R. M. (2003). Primary productivity of reef-building crustose coralline algae. Limnology and Oceanography 48, 1376–1387.
Primary productivity of reef-building crustose coralline algae.Crossref | GoogleScholarGoogle Scholar |

Day, J. (2008). The need and practice of monitoring, evaluating and adapting marine planning and management-lessons from the Great Barrier Reef. Marine Policy 32, 823–831.
The need and practice of monitoring, evaluating and adapting marine planning and management-lessons from the Great Barrier Reef.Crossref | GoogleScholarGoogle Scholar |

Doney, S. C., Ruckelshaus, M., Duffy, E. J., Barry, J. P., Chan, F., English, C. A., Galindo, H. M., Grebmeier, J. M., Hollowed, A. B., Knowlton, N., Polovina, J., Rabalais, N. N., Sydeman, W. J., and Talley, L. D. (2012). Climate change impacts on marine ecosystems. Annual Review of Marine Science 4, 11–37.
Climate change impacts on marine ecosystems.Crossref | GoogleScholarGoogle Scholar | 22457967PubMed |

Doropoulos, C., Ward, S., Diaz-Pulido, G., Hoegh-Guldberg, O., and Mumby, P. J. (2012). Ocean acidification reduces coral recruitment by disrupting intimate larval-algal settlement interactions. Ecology Letters 15, 338–346.
Ocean acidification reduces coral recruitment by disrupting intimate larval-algal settlement interactions.Crossref | GoogleScholarGoogle Scholar |

Fabricius, K., and De’ath, G. (2001). Environmental factors associated with the spatial distribution of crustose coralline algae on the Great Barrier Reef. Coral Reefs 19, 303–309.
Environmental factors associated with the spatial distribution of crustose coralline algae on the Great Barrier Reef.Crossref | GoogleScholarGoogle Scholar |

Gachon, C. M. M., Sime-Ngando, T., Strittmatter, M., Chambouvet, A., and Kim, G. H. (2010). Algal diseases: spotlight on a black box. Trends in Plant Science 15, 633–640.
Algal diseases: spotlight on a black box.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtlyku77O&md5=3d2eaac3b1def6dafb5970754b811fa8CAS |

Gladfelter, W. B. (1982). White band disease in Acropora palmata: implications for the structure and growth of shallow reefs. Bulletin of Marine Science 32, 639–643.

Harrington, L., Fabricius, K., De’ath, G., and Negri, A. (2004). Recognition and selection of settlement substrata determine post-settlement survival in corals. Ecology 85, 3428–3437.
Recognition and selection of settlement substrata determine post-settlement survival in corals.Crossref | GoogleScholarGoogle Scholar |

Harvell, C. D., Jordán-Dahlgren, E., Merkel, S., Rosenberg, E., Raymundo, L., Smith, G,, Weil, E., and Willis, B. (2007). Coral disease, environmental drivers, and the balance between coral and microbial associates. Oceanography and Marine Biology – an Annual Review 20, 58–81.

Harvell, D., Altizer, S., Cattadori, I. M., and Harrington, L. (2009). Climate change and wildlife diseases: when does the host matter the most? Ecology 90, 912–920.
Climate change and wildlife diseases: when does the host matter the most?Crossref | GoogleScholarGoogle Scholar | 19449685PubMed |

Heron, S. F., Willis, B. L., Skirving, W. J., Eakin, C. M., Page, C. A., and Miller, I. R. (2010). Summer hot snaps and winter conditions: modelling white syndrome outbreaks on Great Barrier Reef corals. PLoS ONE 5, e12210.
Summer hot snaps and winter conditions: modelling white syndrome outbreaks on Great Barrier Reef corals.Crossref | GoogleScholarGoogle Scholar | 20808912PubMed |

Heyward, A. J., and Negri, A. P. (1999). Natural inducers for coral larval metamorphosis. Coral Reefs 18, 273–279.
Natural inducers for coral larval metamorphosis.Crossref | GoogleScholarGoogle Scholar |

Jones, R. J., Bowyer, J., Hoegh-Guldberg, O., and Blackall, L. L. (2004). Dynamics of a temperature-related coral disease outbreak. Marine Ecology Progress Series 281, 63–77.
Dynamics of a temperature-related coral disease outbreak.Crossref | GoogleScholarGoogle Scholar |

Jonker, M., Johns, K., and Osborne, K. (2008). Surveys of benthic reef communities using underwater digital photography and counts of juvenile corals. Long-term monitoring of the Great Barrier Reef. Standard operational procedure no. 10. Australian Institute of Marine Science, Townsville, Qld.

Knowlton, N., and Jackson, J. B. C. (2008). Shifting baselines, local impacts, and global change on coral reefs. PLoS Biology 6, e54.
Shifting baselines, local impacts, and global change on coral reefs.Crossref | GoogleScholarGoogle Scholar | 18303956PubMed |

Kuffner, I. B., Andersson, A. J., Jokiel, P. L., Rodgers, K., and Mackenzie, F. T. (2008). Decreased abundance of crustose coralline algae due to ocean acidification. Nature Geoscience 1, 114–117.
Decreased abundance of crustose coralline algae due to ocean acidification.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXjsVGjs7g%3D&md5=ea0a98f7ae2349d50407e1019223ee97CAS |

Lambert, D. (1992). Zero-inflated Poisson regression, with an application to defects in manufacturing. Technometrics 34, 1–14.
Zero-inflated Poisson regression, with an application to defects in manufacturing.Crossref | GoogleScholarGoogle Scholar |

Littler, M. M., and Littler, D. S. (1995). Impact of CLOD Pathogen on Pacific Coral Reefs. Science 267, 1356–1360.
| 1:CAS:528:DyaK2MXktF2it78%3D&md5=c3f7b22d1fa4b8203a115c6d4bf18112CAS | 17812612PubMed |

Littler, M. M., and Littler, D. S. (1998). An undescribed fungal pathogen of reef-forming crustose coralline algae discovered in American Samoa. Coral Reefs 17, 144.
An undescribed fungal pathogen of reef-forming crustose coralline algae discovered in American Samoa.Crossref | GoogleScholarGoogle Scholar |

Littler, M. M., and Littler, D. S. (2003). ‘South Pacific Reef Plants: a Diver’s Guide to Plant Life of South Pacific Coral Reefs.’ (Offshore Graphics: Washington, DC.)

Martin, S. E., and Gattuso, J. P. (2009). Response of Mediterranean coralline algae to ocean acidification and elevated temperature. Global Change Biology 15, 2089–2100.
Response of Mediterranean coralline algae to ocean acidification and elevated temperature.Crossref | GoogleScholarGoogle Scholar |

Miller, I., and Dolman, A. (2009). Relative role of disease and predators as drivers of decline in coral cover on the Great Barrier Reef. In ‘Proceedings of the 11th International Coral Reef Symposium, Fort Lauderdale, 7–11 July 2008’. Riegl, B. M., and Dodge R. E. (eds) Volume 1, Session number 6. pp. 216–220. (National Coral Reef Initiative, Nova South Eastern University, Florida.)

Miller, I. R., Jonker, M., and Coleman, G. (2009). Crown-of-thorns starfish and coral surveys using the manta tow and SCUBA search techniques. Standard operational procedure no. 9(3). Australian Institute of Marine Science, Townsville, Qld.

Nugues, M. N. (2002). Impact of a coral disease outbreak on coral communities in St Lucia: what and how much has been lost? Marine Ecology Progress Series 229, 61–71.
Impact of a coral disease outbreak on coral communities in St Lucia: what and how much has been lost?Crossref | GoogleScholarGoogle Scholar |

O’Leary, J. K., and McClanahan, T. R. (2010). Trophic cascades result in large-scale coralline algae loss through differential grazer effects. Ecology 91, 3584–3597.
Trophic cascades result in large-scale coralline algae loss through differential grazer effects.Crossref | GoogleScholarGoogle Scholar | 21302830PubMed |

Patterson, K. L., Porter, J. W., Ritchie, K. B., and Polson, S. W. (2002). The etiology of white pox, a lethal disease of the Caribbean elkhorn coral Acropora palmata. Proceedings of the National Academy of Sciences of the United States of America 99, 8725–8730.
The etiology of white pox, a lethal disease of the Caribbean elkhorn coral Acropora palmata.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XltF2hsbg%3D&md5=94d38fdffaf7a15c4aca70433c1def97CAS | 12077296PubMed |

R Development Core Team (2011). ‘R: a Language and Environment for Statistical Computing.’ (R Foundation for Statistical Computing: Vienna.) Available at http://www.R-project.org/ [Accessed 20 November 2012].

Rasser, M. W., and Riegl, B. (2002). Holocene coral reef rubble and its binding agents. Coral Reefs 21, 57–72.

Sandin, S. A., Smith, J. E., DeMartini, E. E., Dinsdale, E. A., Donner, S. D., Friedlander, A. M., Konotchick, T., Malay, M., Maragos, J. E., Obura, D., Pantos, O., Paulay, G., Richie, M., Rohwer, F., Schroeder, R. E., Walsh, S., Jackson, J. B. C., Knowlton, N., and Sala, E. (2008). Baselines and degradation of coral reefs in the Northern Line Islands. PLoS ONE 3, e1548.
Baselines and degradation of coral reefs in the Northern Line Islands.Crossref | GoogleScholarGoogle Scholar | 18301734PubMed |

Santavy, D. L., Peters, E. C., Quirolo, C., Porter, J. W., and Bianchi, C. N. (1999). Yellow-blotch disease outbreaks on reefs of the San Blas Islands, Panama. Coral Reefs 18, 97.

Skaug, H., Fournier, D., Nielsen, A., Magnusson, A., and Bolker, B. (2011). ‘glmmADMB: Generalized Linear Mixed Models Using AD Model Builder.’ Available at http://R-Forge.R-project.org/projects/glmmadmb/ [Accessed 20 November 2012].

Steneck, R. S. (1986). The ecology of coralline algal crusts: convergent patterns of adaptive strategies. Annual Review of Ecology and Systematics 17, 273–303.
The ecology of coralline algal crusts: convergent patterns of adaptive strategies.Crossref | GoogleScholarGoogle Scholar |

Sweatman, H., Cheal, A., Coleman, G., Emslie, M., Johns, K., Jonker, M., Miller, I., and Osborne, K. (2008). Long-term monitoring of the Great Barrier Reef. Status report no. 8. Australian Institute of Marine Science, Townsville, Qld.

Tribollet, A., Aeby, G., and Work, T. (2011). Survey and determination of coral and coralline algae diseases/lesions in the lagoon of New Caledonia. Studies of coral diseases in New Caledonia. Coral Reef Initiatives for the Pacific, Noumea, New Caledonia.

Vargas-Ángel, B. (2010). Crustose coralline algal diseases in the US-affiliated Pacific islands. Coral Reefs 29, 943–956.
Crustose coralline algal diseases in the US-affiliated Pacific islands.Crossref | GoogleScholarGoogle Scholar |

Williams, D. E., and Miller, M. W. (2005). Coral disease outbreak: pattern, prevalence and transmission in Acropora cervicornis. Marine Ecology Progress Series 301, 119–128.
Coral disease outbreak: pattern, prevalence and transmission in Acropora cervicornis.Crossref | GoogleScholarGoogle Scholar |

Willis, B. L., Page, C. A., and Dinsdale, E. A. (2004). Coral disease on the Great Barrier Reef. In ‘Coral Health and Disease’. (Eds E. Rosenberg and Y. Loya.) pp. 69–104. (Springer-Verlag: Berlin.)

Wobeser, G. A. (2006). ‘Essentials of Disease in Wild Animals.’ (Blackwell Publishing: Ames, IA.)