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Advances in the aquatic sciences
RESEARCH ARTICLE

Prevalence of tissue necrosis and brown spot lesions in a common marine sponge

Heidi M. Luter A B C D , Steve Whalan B and Nicole S. Webster B
+ Author Affiliations
- Author Affiliations

A School of Marine and Tropical Biology, James Cook University, Townsville, Qld 4811, Australia.

B Australian Institute of Marine Science, PMB 3, Townsville, Qld 4810, Australia.

C AIMS@JCU, James Cook University, Townsville, Qld 4811, Australia.

D Corresponding author. Email: heidi.luter@jcu.edu.au

Marine and Freshwater Research 61(4) 484-489 https://doi.org/10.1071/MF09200
Submitted: 13 August 2009  Accepted: 12 October 2009   Published: 27 April 2010

Abstract

Sponges form a highly diverse and ecologically significant component of benthic communities. Despite their importance, disease dynamics in sponges remain relatively unexplored. There are reports of severe disease epidemics in sponges from the Caribbean and the Mediterranean; however, extensive sponge mortalities have not yet been reported from the Great Barrier Reef (GBR) and Torres Strait, north-eastern Australia. Marine sponge surveys were conducted in the Palm Islands on the central GBR and Masig Island, Torres Strait, to determine the health of the Demosponge Ianthella basta. Using tissue necrosis and the presence of brown lesions as a proxy of health, sponges were assigned to predetermined disease categories. Sponges with lesions were present at all sites with 43 and 66% of I. basta exhibiting lesions and symptoms of necrosis in the Palm Islands and Torres Strait, respectively. Sponges from the Torres Strait also showed a greater incidence of significant and extensive necrosis in comparison to sponges from Palm Island (11.5 v. 6%). These results indicate the widespread distribution of a disease-like syndrome affecting the health of I. basta, and highlight the critical need for regular monitoring programs and future research to assess patterns in disease dynamics and ascertain the etiological agents of infection.

Additional keywords: injury, Porifera, stress, tropical.


Acknowledgements

We thank R. de Nys for his support and editing contributions, as well as three anonymous referees. We also thank C. Wolff, L. Evans-Illidge, K. Johns and J. Morris for diving and fieldwork. We also acknowledge the technical, scientific and financial assistance from the Australian Microscopy and Microanalysis Research Facility. This work was supported by an AIMS@JCU and Marine and Tropical Sciences Research Facility postgraduate award to H.M.L. All work in the Palm Islands was completed under the Great Barrier Reef Marine Park Authority Permit Number GO6/15571.1.


References

Ainsworth, T. D. , Kramasky-Winter, E. , Loya, Y. , Hoegh-Guldberg, O. , and Fine, M. (2007). Coral disease diagnostics: What’s between a plague and a band? Applied and Environmental Microbiology 73, 981–992.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | Gochfeld D. J., Schloeder C., and Thacker R. W. (2007). Sponge community structure and disease prevalence on coral reefs in Bocas del Toro, Panama. In ‘Museu Nacional Serie Livros., Rio de Janeiro, 7–13 May 2006’. (Eds M. R. Custódio, G. Lôbo-Hajdu, E. Hajdu and G. Muricy.) pp. 335–343. (Museu Nacional-Univ Federal Do: Rio de Janeiro.)

Harvell, C. D. , Mitchell, C. E. , Ward, R. W. , Altizer, S. , Dobson, A. P. , Ostfeld, R. S. , and Samuel, M. D. (2002). Climate warming and disease risks for terrestrial and marine biota. Science 296, 2158–2162.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | Hooper J. N. A., and Van Soest R. W. M. (2002). ‘Systema Porifera: A Guide to the Classification of Sponges.’ (Kluwer Academic/Plenum Publishers: New York.)

Hooper J. N. A., and Weidenmayer F. (1994). Porifera. In ‘Zoological Catalogue of Australia, Vol. 12’. (Ed. A. Wells.) pp. 1–621. (CSIRO Publishing: Melbourne.)

Jones, R. J. , Bowyer, J. , Hoegh-Gulberg, O. , and Blackall, L. L. (2004). Dynamics of a temperature-related coral disease outbreak. Marine Ecology Progress Series 281, 63–77.
Crossref | GoogleScholarGoogle Scholar | Kinne O. (1980). Diseases of marine animals: general aspects. In ‘Diseases of Marine Animals’. (Ed. O. Kinne.) pp. 13–73. (John Wiley and Sons: Chichester, UK.)

Knowlton, A. L. , and Highsmith, R. C. (2005). Nudibranch-sponge feeding dynamics: benefits of symbiont-containing sponge to Archidoris montereyensis (Cooper, 1862) and recovery of nudibranch feeding scars by Halichondria panicea (Pallas, 1766). Journal of Experimental Marine Biology and Ecology 327, 36–46.
Crossref | GoogleScholarGoogle Scholar | Nagelkerken I., Aerts L., and Pors L. (2000). Barrel sponge bows out. In ‘Reef Encounter’. (Ed. S. Wells.) pp. 14–15. (International Society for Reef Studies: Lawrence, KA.)

Negri, A. P. , Soo, R. M. , Flores, F. , and Webster, N. S. (2009). Bacillus insecticides are not acutely harmful to corals and sponges. Marine Ecology Progress Series 381, 157–165.
Crossref | GoogleScholarGoogle Scholar | CAS | Simpson T. L. (1984). ‘The Cell Biology of Sponges.’ (Springer-Verlag: New York.)

Vacelet J. (1994). Control of the severe sponge epidemic – Near East and Europe: Algeria, Cyprus, Egypt, Lebanon, Malta, Morocco, Syria, Tunisia, Turkey, Yugoslavia. Technical Report – the struggle against the epidemic which is decimating Mediterranean sponges FI: TCP/RAB/8853. FAO, Rome.

Van Soest R. W. M., Boury-Esnault N., Hooper J. N. A., Rützler K., de Voogd N. J., et al. (2008). World Porifera database. Available at http://www.marinespecies.org/porifera [Accessed 15 July 2009].

Webster, N. S. (2007). Sponge disease: a global threat? Environmental Microbiology 9, 1363–1375.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | Zar J. H. (1999). ‘Biostatistical Analysis.’ (Prentice Hall: New Jersey.)