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Bioeroding sponge assemblages: the importance of substrate availability and sediment

Published online by Cambridge University Press:  22 March 2018

Joseph Marlow
Victoria University of Wellington, School of Biological Sciences, Wellington, 6140, New Zealand
Christine H.L. Schönberg
School of Earth and Environment and Oceans Institute, University of Western Australia, Crawley, WA 6009, Australia
Simon K. Davy
Victoria University of Wellington, School of Biological Sciences, Wellington, 6140, New Zealand
Abdul Haris
Research and Development Centre on Marine, Coastal and Small Islands, Hasanuddin University, Makassar, Indonesia
Jamaluddin Jompa
Research and Development Centre on Marine, Coastal and Small Islands, Hasanuddin University, Makassar, Indonesia
James J. Bell
Victoria University of Wellington, School of Biological Sciences, Wellington, 6140, New Zealand
E-mail address:


Despite global deterioration of coral reef health, not all reef-associated organisms are in decline. Bioeroding sponges are thought to be largely resistant to the factors that stress and kill corals, and are increasing in abundance on many reefs. However, there is a paucity of information on how environmental factors influence spatial variation in the distribution of these sponges, and how they might be affected by different stressors. We aimed to identify the factors that explained differences in bioeroding sponge abundance and assemblage composition, and to determine whether bioeroding sponges benefit from the same environmental conditions that can contribute towards coral mortality. Abundance surveys were conducted in the Wakatobi region of Indonesia on reefs characterized by different biotic and abiotic conditions. Bioeroding sponges occupied an average of 8.9% of available dead substrate and variation in abundance and assemblage composition was primarily attributed to differences in the availability of dead substrate. Our results imply that if dead substrate availability increases as a consequence of coral mortality, bioeroding sponge abundance is also likely to increase. However, bioeroding sponge abundance was lowest on a sedimented reef, despite abundant dead substrate. This suggests that not all forms of coral mortality will benefit all bioeroding sponge species, and sediment-degraded reefs are likely to be dominated by a few resilient bioeroding sponge species. Overall, we demonstrate the importance of understanding the drivers of bioeroding sponge abundance and assemblage composition in order to predict possible impacts of different stressors on reefs communities.

Research Article
Copyright © Marine Biological Association of the United Kingdom 2018 

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Alvarez-Filip, L, Gill, JA, Dulvy, N.K., Perry, A.L., Watkinson, A.R. and Côté, I.M. (2011) Drivers of region-wide declines in architectural complexity on Caribbean reefs. Coral Reefs 30, 10511060.CrossRefGoogle Scholar
Anderson, M., Gorley, R. and Clarke, K. (2008) PERMANOVA for PRIMER: guide to software and statistical methods. Plymouth: PRIMER-E.Google Scholar
Bannister, R., Battershill, C. and de Nys, R. (2012) Suspended sediment grain size and mineralogy across the continental shelf of the Great Barrier Reef: impacts on the physiology of a coral reef sponge. Continental Shelf Research 32, 8695.CrossRefGoogle Scholar
Bautista-Guerrero, E., Carballo, J.L., Aguilar-Camacho, J.M. and Sifuentes-Romero, I. (2016) Molecular and morphological differentiation of sympatric larvae of coral excavating sponges of genus Thoosa. Zoomorphology 135, 159165.CrossRefGoogle Scholar
Bautista-Guerrero, E., Carballo, J.L. and Maldonado, M. (2010) Reproductive cycle of the coral-excavating sponge Thoosa mismalolli (Clionaidae) from Mexican Pacific coral reefs. Invertebrate Biology 129, 285296.CrossRefGoogle Scholar
Bell, J.J., Davy, S.K., Jones, T., Taylor, M.W. and Webster, N.S. (2013) Could some coral reefs become sponge reefs as our climate changes? Global Change Biology 19, 26132624.CrossRefGoogle ScholarPubMed
Bell, J.J., McGrath, E., Biggerstaff, A., Bates, T., Bennett, H., Marlow, J. and Shaffer, M. (2015) Sediment impacts on marine sponges. Marine Pollution Bulletin 94, 513.CrossRefGoogle ScholarPubMed
Bell, J.J. and Smith, D. (2004) Ecology of sponge assemblages (Porifera) in the Wakatobi region, south-east Sulawesi, Indonesia: richness and abundance. Journal of the Marine Biological Association of the United Kingdom 84, 581591.CrossRefGoogle Scholar
Bell, J.J. and Turner, J.R. (2000) Factors influencing the density and morphometrics of the cup coral Caryophyllia smithii in Lough Hyne. Journal of the Marine Biological Association of the United Kingdom 80, 437441.CrossRefGoogle Scholar
Bergman, K.M. (1983) Distribution and ecological significance of the boring sponge Cliona viridis on the Great Barrier Reef, Australia. MSc thesis. McMaster University, Hamilton, Ontario, Canada.Google Scholar
Biggerstaff, A., Smith, D.J., Jompa, J. and Bell, J.J. (2015) Photoacclimation supports environmental tolerance of a sponge to turbid low-light conditions. Coral Reefs 34, 10491061.CrossRefGoogle Scholar
Biggerstaff, A., Smith, D.J., Jompa, J. and Bell, J.J. (2017) Metabolic responses of a phototrophic sponge to sedimentation supports transitions to sponge-dominated reefs. Scientific Reports 7, 2725.CrossRefGoogle ScholarPubMed
Bruno, J.F. and Selig, E.R. (2007) Regional decline of coral cover in the Indo-Pacific: timing, extent, and subregional comparisons. PLoS ONE 2, e711.CrossRefGoogle ScholarPubMed
Bruno, J.F., Sweatman, H., Precht, W.F., Selig, E.R. and Schutte, V.G. (2009) Assessing evidence of phase shifts from coral to macroalgal dominance on coral reefs. Ecology 90, 14781484.CrossRefGoogle ScholarPubMed
Burke, L.M., Reytar, K., Spalding, M. and Perry, A. (2011) Reefs at risk revisited. Washington, DC: World Resources Institute.Google Scholar
Burnham, K.P. and Anderson, D.R. (2004) Multimodel inference: understanding AIC and BIC in model selection. Sociological Methods and Research 33, 261304.CrossRefGoogle Scholar
Büttner, E. and Siebler, F. (2013) The impact of simulated dredging on sponges from the East Australian coastal line. Habilitation thesis. University of Stuttgart, Germany.Google Scholar
Calcinai, B., Azzini, F., Bavestrello, G., Cerrano, C., Pansini, M. and Thung, D.C. (2006) Boring sponges from the Ha Long Bay, Tonkin Gulf, Vietnam. Zoological Studies 45, 201212.Google Scholar
Calcinai, B., Bavestrello, G. and Cerrano, C. (2005) Excavating sponge species from the Indo-Pacific Ocean. Zoological Studies 44, 518.Google Scholar
Calcinai, B., Bavestrello, G., Cerrano, C. and Gaggero, L. (2008) Substratum microtexture affects the boring pattern of Cliona albimarginata (Clionaidae, Demospongiae). In Wisshak, M. and Tapanila, L. (eds) Current developments in bioerosion. Berlin: Springer, pp. 203211.CrossRefGoogle Scholar
Callahan, M.K. (2005) Distribution of clionid sponges in the Florida Keys National Marine Sanctuary (FKNMS), 2001–2003. MSc thesis. University of South Florida, Tampa, USA.Google Scholar
Carballo, J.L., Bautista-Guerrero, E. and Leyte-Morales, G.E. (2008) Boring sponges and the modelling of coral reefs in the east Pacific Ocean. Marine Ecology Progress Series 356, 113122.CrossRefGoogle Scholar
Carballo, J.L., Bautista, E., Nava, H., Cruz-Barraza, J.A. and Chávez, J.A. (2013) Boring sponges, an increasing threat for coral reefs affected by bleaching events. Ecology and Evolution 3, 872886.CrossRefGoogle ScholarPubMed
Carballo, J.L., Sanchez-Moyano, J.E. and García-Gómez, J.C. (1994) Taxonomic and ecological remarks on boring sponges (Clionidae) from the straits of Gibraltar (southern Spain): tentative bioindicators? Zoological Journal of the Linnean Society 112, 407424.CrossRefGoogle Scholar
Chaves-Fonnegra, A., Feldheim, K.A., Secord, J. and Lopez, J.V. (2015) Population structure and dispersal of the coral-excavating sponge Cliona delitrix. Molecular Ecology 24, 14471466.CrossRefGoogle ScholarPubMed
Chaves-Fonnegra, A. and Zea, S. (2007) Observations on reef coral undermining by the Caribbean excavating sponge Cliona delitrix (Demospongiae, Hadromerida). In Custódio, M.R., Lôbo-Hajdu, G., Hajdu, E. and Muricy, G. (eds) Porifera research. Biodiversity, innovation and sustainability. Rio de Janeiro: National Museum, pp. 247254.Google Scholar
Chaves-Fonnegra, A., Zea, S. and Gómez, M.L. (2007) Abundance of the excavating sponge Cliona delitrix in relation to sewage discharge at San Andrés Island, SW Caribbean, Colombia. Boletín de Investigaciones Marinas y Costeras 36, 6378.Google Scholar
Cheal, A., MacNeil, M.A., Cripps, E., Emslie, M., Jonker, M., Schaffelke, B. and Sweatman, H. (2010) Coral-macroalgal phase shifts or reef resilience: links with diversity and functional roles of herbivorous fishes on the Great Barrier Reef. Coral Reefs 29, 10051015.CrossRefGoogle Scholar
Clarke, K.R. and Gorley, R.N. (2006) PRIMER v6: user manual/tutorial. Plymouth: PRIMER-E.Google Scholar
Clarke, K.R., Somerfield, P.J. and Chapman, M.G. (2006) On resemblance measures for ecological studies, including taxonomic dissimilarities and a zero-adjusted Bray–Curtis coefficient for denuded assemblages. Journal of Experimental Marine Biology and Ecology 330, 5580.CrossRefGoogle Scholar
Cooper, T.F., Ridd, P.V., Ulstrup, K.E., Humphrey, C., Slivkoff, M. and Fabricius, K.E. (2008) Temporal dynamics in coral bioindicators for water quality on coastal coral reefs of the Great Barrier Reef. Marine and Freshwater Research 59, 703716.CrossRefGoogle Scholar
Crabbe, J.M. and Smith, D.J. (2002) Comparison of two reef sites in the Wakatobi Marine National Park (SE Sulawesi, Indonesia) using digital image analysis. Coral Reefs 21, 242244.CrossRefGoogle Scholar
Crabbe, J.M. and Smith, D.J. (2005) Sediment impacts on growth rates of Acropora and Porites corals from fringing reefs of Sulawesi, Indonesia. Coral Reefs 24, 437441.CrossRefGoogle Scholar
Cullen, L.C., Pretty, J., Smith, D. and Pilgrim, S.E. (2007) Links between local ecological knowledge and wealth in indigenous communities of Indonesia: implications for conservation of marine resources. International Journal of Interdisciplinary Social Sciences 2, 289299.CrossRefGoogle Scholar
De'ath, G. and Fabricius, K.E. (2010) Water quality as a regional driver of coral biodiversity and macroalgae on the Great Barrier Reef. Ecological Applications 20, 840850.CrossRefGoogle ScholarPubMed
De'ath, G., Fabricius, K.E., Sweatman, H. and Puotinen, M. (2012) The 27-year decline of coral cover on the Great Barrier Reef and its causes. Proceedings of the National Academy of Sciences USA 109, 1799517999.CrossRefGoogle ScholarPubMed
Devlin, M.J., Da Silva, E.T., Petus, C., Wenger, A., Zeh, D., Tracey, D., Álvarez-Romero, J.G. and Brodie, J. (2013) Combining in-situ water quality and remotely sensed data across spatial and temporal scales to measure variability in wet season chlorophyll-a: Great Barrier Reef lagoon (Queensland, Australia). Ecological Processes 2, 31.CrossRefGoogle Scholar
Doty, M.S. (1971) Measurement of water movement in reference to benthic algal growth. Botanica Marina 14, 3235.CrossRefGoogle Scholar
Edinger, E.N., Limmon, G.V., Jompa, J., Widjatmoko, W., Heikoop, J.M. and Risk, M.J. (1998) Reef degradation and coral biodiversity in Indonesia: effects of land-based pollution, destructive fishing practices and changes over time. Marine Pollution Bulletin 36, 617630.CrossRefGoogle Scholar
Edinger, E.N., Limmon, G.V., Jompa, J., Widjatmoko, W., Heikoop, J.M. and Risk, M.J. (2000) Normal coral growth rates on dying reefs: are coral growth rates good indicators of reef health? Marine Pollution Bulletin 40, 404425.CrossRefGoogle Scholar
Edinger, E.N. and Risk, M.J. (2013) Effect of land-based pollution on central Java coral reefs. Journal of Coastal Development 3, 593613.Google Scholar
English, S.S., Wilkinson, C.C. and Baker, V.V. (1994) Survey manual for tropical marine resources. Line intercept transect. Townsville: Australian Institute of Marine Science, pp. 3451.Google Scholar
Enochs, I.C. and Manzello, D.P. (2012) Species richness of motile cryptofauna across a gradient of reef framework erosion. Coral Reefs 31, 653661.CrossRefGoogle Scholar
Erftemeijer, P.L., Riegl, B., Hoeksema, B.W. and Todd, P.A. (2012) Environmental impacts of dredging and other sediment disturbances on corals: a review. Marine Pollution Bulletin 64, 17371765.CrossRefGoogle ScholarPubMed
Fabricius, K.E. (2005) Effects of terrestrial runoff on the ecology of corals and coral reefs: review and synthesis. Marine Pollution Bulletin 50, 125146.CrossRefGoogle ScholarPubMed
Fabricius, K.E. (2011) Factors determining the resilience of coral reefs to eutrophication: a review and conceptual model. In Dubinsky, Z. and Stambler, N. (eds) Coral reefs: an ecosystem in transition. Dordrecht: Springer, pp. 493505.CrossRefGoogle Scholar
Fang, J.K.H., Schönberg, C.H.L., Hoegh-Guldberg, O. and Dove, S. (2017) Symbiotic plasticity of Symbiodinium in a common excavating sponge. Marine Biology 164, 104.CrossRefGoogle Scholar
Fang, J.K.H., Schönberg, C.H.L., Mello-Athayde, M.A., Hoegh-Guldberg, O. and Dove, S. (2014) Effects of ocean warming and acidification on the energy budget of an excavating sponge. Global Change Biology 20, 10431054.CrossRefGoogle ScholarPubMed
Glynn, P.W. (1997) Bioerosion and coral-reef growth: a dynamic balance. In Birkeland, C. (ed.) Life and death of coral reefs. New York, NY: Springer, pp. 6895.CrossRefGoogle Scholar
Golbuu, Y., Van Woesik, R., Richmond, R.H., Harrison, P. and Fabricius, K.E. (2011) River discharge reduces reef coral diversity in Palau. Marine Pollution Bulletin 62, 824831.CrossRefGoogle ScholarPubMed
González-Rivero, M., Yakob, L. and Mumby, P.J. (2011) The role of sponge competition on coral reef alternative steady states. Ecological Modelling 222, 18471853.CrossRefGoogle Scholar
Graham, N.A. and Nash, K.L. (2012) The importance of structural complexity in coral reef ecosystems. Coral Reefs 32, 315326.CrossRefGoogle Scholar
Hennige, S.J., Smith, D.J., Perkins, R., Consalvey, M., Paterson, D.M. and Suggett, D.J. (2008) Photoacclimation, growth and distribution of massive coral species in clear and turbid waters. Marine Ecology Progress Series 369, 7788.CrossRefGoogle Scholar
Hennige, S.J., Smith, D.J., Walsh, S.J., McGinley, M.P., Warner, M. E. and Suggett, D.J. (2010) Acclimation and adaptation of scleractinian coral communities along environmental gradients within an Indonesian reef system. Journal of Experimental Marine Biology and Ecology 391, 143152.CrossRefGoogle Scholar
Holmes, K.E., Edinger, E.N., Limmon, G.V. and Risk, M.J. (2000) Bioerosion of live massive corals and branching coral rubble on Indonesian coral reefs. Marine Pollution Bulletin 40, 606617.CrossRefGoogle Scholar
Holmes, G., Ortiz, J.C. and Schönberg, C.H.L. (2009) Bioerosion rates of the sponge Cliona orientalis Thiele, 1900: spatial variation over short distances. Facies 55, 203311.CrossRefGoogle Scholar
Hughes, T., Szmant, A.M., Steneck, R., Carpenter, R. and Miller, S. (1999) Algal blooms on coral reefs: what are the causes? Limnology and Oceanography 44, 15831586.CrossRefGoogle Scholar
Jokiel, P.L. and Morrissey, J.I. (1993) Water motion on coral reefs – evaluation of the clod card technique. Marine Ecology Progress Series 93, 175181.CrossRefGoogle Scholar
Kennedy, E.V., Perry, C.T., Halloran, P.R., Fine, M., Carricart-Ganivet, J.P., Iglesias-Prieto, R., Form, A., Wisshak, M., Schönberg, C.H.L. and Mumby, P.J. (2013) Avoiding coral structural collapse requires local and global action. Current Biology 23, 912918.CrossRefGoogle ScholarPubMed
Lapointe, B.E., Barile, P.J. and Matzie, W.R. (2004) Anthropogenic nutrient enrichment of seagrass and coral reef communities in the Lower Florida Keys: discrimination of local versus regional nitrogen sources. Journal of Experimental Marine Biology and Ecology 308, 2358.CrossRefGoogle Scholar
Lindgren, N.G. (1897) Beitrag zur Kenntniss der Spongienfauna des Malaiischen Archipels und der Chinesischen Meere. Zoologischer Anzeiger 547, 480487.Google Scholar
López-Victoria, M. and Zea, S. (2004) Storm-mediated coral colonization by an excavating Caribbean sponge. Climate Research 26, 251256.CrossRefGoogle Scholar
López-Victoria, M. and Zea, S. (2005) Current trends of space occupation by encrusting excavating sponges on Colombian coral reefs. Marine Ecology 26, 3341.CrossRefGoogle Scholar
Mallela, J. and Perry, C. (2007) Calcium carbonate budgets for two coral reefs affected by different terrestrial runoff regimes, Rio Bueno, Jamaica. Coral Reefs 26, 129145.CrossRefGoogle Scholar
Mariani, S., Uriz, M.J. and Turon, X. (2000) Larval bloom of the oviparous sponge Cliona viridis: coupling of larval abundance and adult distribution. Marine Biology 137, 783790.CrossRefGoogle Scholar
Marlow, J., Smith, D., Werorilang, S. and Bell, J. (in press) Sedimentation limits the erosion rate of a bioeroding sponge. Marine Ecology e12483 doi: 10.1111/maec.12483.Google Scholar
McManus, J.W. and Polsenberg, J.F. (2004) Coral-algal phase shifts on coral reefs: ecological and environmental aspects. Progress in Oceanography 60, 263279.CrossRefGoogle Scholar
McMellor, S. and Smith, D.J. (2010) Coral reefs of the Wakatobi: abundance and biodiversity. In Clifton, J., Unsworth, R.K.F. and Smith, D.J. (eds) Marine research and conservation in the Coral Triangle: the Wakatobi National Park. New York, NY: Nova Publishers, pp. 1126.Google Scholar
Mueller, B., de Goeij, J.M., Vermeij, M.J., Mulders, Y., van der Ent, E., Ribes, M. and van Duyl, F.C. (2014) Natural diet of coral-excavating sponges consists mainly of dissolved organic carbon (DOC). PLoS ONE 9, e90152.CrossRefGoogle Scholar
Mumby, P.J. (2009) Phase shifts and the stability of macroalgal communities on Caribbean coral reefs. Coral Reefs 28, 761773.CrossRefGoogle Scholar
Muricy, G. (1991) Structure des peuplements de spongiaires autour de l'égout de Cortiou (Marseille, France). Vie et Milieu 41, 205221.Google Scholar
Nava, H. and Carballo, J.L. (2008) Chemical and mechanical bioerosion of boring sponges from Mexican Pacific coral reefs. Journal of Experimental Biology 211, 28272831.CrossRefGoogle ScholarPubMed
Nava, H. and Carballo, J.L. (2013) Environmental factors shaping boring sponge assemblages at Mexican Pacific coral reefs. Marine Ecology 34, 269279.CrossRefGoogle Scholar
Nava, H., Ramírez-Herrera, M.T., Figueroa-Camacho, A.G. and Villegas-Sanchez, B.M. (2014) Habitat characteristics and environmental factors related to boring sponge assemblages on coral reefs near populated coastal areas on the Mexican eastern Pacific coast. Marine Biodiversity 44, 4554.CrossRefGoogle Scholar
Norström, A.V., Nyström, M., Lokrantz, J. and Folke, C. (2009) Alternative states on coral reefs: beyond coral-macroalgal phase shifts. Marine Ecology Progress Series 376, 295306.CrossRefGoogle Scholar
Ogston, A.S., Storlazzi, C.D., Field, M.E. and Presto, M.K. (2004) Sediment resuspension and transport patterns on a fringing reef flat, Molokai, Hawaii. Coral Reefs 23, 559569.Google Scholar
Pang, R.K. (1973) The ecology of some Jamaican excavating sponges. Bulletin of Marine Science 23, 227243.Google Scholar
Perry, C.T., Spencer, T. and Kench, P. (2008) Carbonate budgets and reef production states: a geomorphic perspective on the ecological phase-shift concept. Coral Reefs 27, 853866.CrossRefGoogle Scholar
Pineda, M.C., Strehlow, B., Duckworth, A., Doyle, J., Jones, R. and Webster, N.S. (2016) Effects of light attenuation on the sponge holobiont – implications for dredging management. Scientific Reports 6, 39038.CrossRefGoogle ScholarPubMed
Pineda, M.C., Strehlow, B., Kamp, J., Duckworth, A., Jones, R. and Webster, N.S. (2017a) Effects of combined dredging-related stressors on sponges: a laboratory approach using realistic scenarios. Scientific Reports 7, 5155.CrossRefGoogle Scholar
Pineda, M.C., Strehlow, B., Sternel, M., Duckworth, A., Haan, J.D., Jones, R. and Webster, N.S. (2017b) Effects of sediment smothering on the sponge holobiont with implications for dredging management. Scientific Reports 7, 5156.CrossRefGoogle Scholar
Pineda, M.C., Strehlow, B., Sternel, M., Duckworth, A., Jones, R. and Webster, N.S. (2017c) Effects of suspended sediments on the sponge holobiont with implications for dredging management. Scientific Reports 7, 4925.CrossRefGoogle Scholar
Pollock, F.J., Lamb, J.B., Field, S.N., Heron, S.F., Schaffelke, B., Shedrawi, G., Bourne, D.G. and Willis, B.L. (2014) Sediment and turbidity associated with offshore dredging increase coral disease prevalence on nearby reefs. PLoS ONE 9, e102498.CrossRefGoogle ScholarPubMed
Powell, A., Smith, D.J., Hepburn, L.J., Jones, T., Berman, J., Jompa, J. and Bell, J.J. (2014) Reduced diversity and high sponge abundance on a sedimented Indo-Pacific reef system: implications for future changes in environmental quality. PLoS ONE 9, e85253.CrossRefGoogle ScholarPubMed
Ramsby, B.D., Hoogenboom, M.O., Whalan, S., Webster, N.S. and Thompson, A. (2017) A decadal analysis of bioeroding sponge cover on the inshore Great Barrier Reef. Scientific Reports 7, 2706.CrossRefGoogle ScholarPubMed
Reis, M.A.C. and Leão, Z.M.A.N. (2000) Bioerosion rate of the sponge Cliona celata (Grant 1826) from reefs in turbid waters, north Bahia, Brazil. In Moosa, M.K., Soemodihardjo, S., Soegiarto, A., Romimohtarto, K., Nontji, A., Soekarno, and Suharsono, (eds) Proceedings of the 9th International Coral Reef Symposium, Bali, Indonesia 23–27 October 2000. Volume 1, pp. 273278.Google Scholar
Reiswig, H.M. (1971) Particle feeding in natural populations of three marine demosponges. Biological Bulletin 141, 568591.CrossRefGoogle Scholar
Risk, M.J., Sammarco, P.W. and Edinger, E.N. (1995) Bioerosion in Acropora across the continental shelf of the Great Barrier Reef Coral Reefs 14, 7986.CrossRefGoogle Scholar
Rose, C.S. and Risk, M.J. (1985) Increase in Cliona delitrix infestation of Montastrea cavernosa heads on an organically polluted portion of the Grand Cayman fringing reef. Marine Ecology 6, 345363.CrossRefGoogle Scholar
Rosell, D. and Uriz, M.J. (1991) Cliona viridis (Schmidt, 1862) and Cliona nigricans (Schmidt, 1862) (Porifera, Hadromerida): evidence which shows they are the same species. Ophelia 33, 4553.CrossRefGoogle Scholar
Rützler, K. (2002) Impact of crustose clionid sponges on Caribbean reef corals. Acta Geologica Hispanica 37, 6172.Google Scholar
Schönberg, C.H.L. (2000) Bioeroding sponges common to the central Australian Great Barrier Reef: descriptions of three new species, two new records, and additions to two previously described species. Senckenbergiana Maritima 30, 161221.CrossRefGoogle Scholar
Schönberg, C.H.L. (2001) Small-scale distribution of Great Barrier Reef bioeroding sponges in shallow water. Ophelia 55, 3954.CrossRefGoogle Scholar
Schönberg, C.H.L. (2002) Substrate effects on the bioeroding demosponge Cliona orientalis. 1. Bioerosion rates. Marine Ecology 23, 313326.CrossRefGoogle Scholar
Schönberg, C.H.L. (2008) A history of sponge erosion: from past myths and hypotheses to recent approaches. In Wisshak, M. and Tapanila, L. (eds) Current developments in bioerosion. Berlin: Springer, pp. 165202.CrossRefGoogle Scholar
Schönberg, C.H.L. (2015a) Monitoring bioeroding sponges: using rubble, quadrat, or intercept surveys? Biological Bulletin 228, 137155.CrossRefGoogle Scholar
Schönberg, C.H.L. (2015b) Self-cleaning surfaces in sponges. Marine Biodiversity 45, 623624.CrossRefGoogle Scholar
Schönberg, C.H.L. (2016a) Happy relationships of marine sponges with sediments – a review and some observations from Australia. Journal of the Marine Biological Association of the United Kingdom 96, 493514.CrossRefGoogle Scholar
Schönberg, C.H.L. (2016b) Project 6.1 – effects of dredging on filter feeder communities, with a focus on sponges. Final report of project 6.1 of the Dredging Science Node of the Western Australian Marine Science Institution, Perth: Australian Institute of Marine Science, 127 pp.Google Scholar
Schönberg, C.H.L., Fang, J.K.H. and Carballo, J.L. (2017a) Bioeroding sponges and the future of coral reefs. In Bell, J.J. and Carballo, J.L. (eds) Climate change, ocean acidification and sponges. Dordrecht: Springer.Google Scholar
Schönberg, C.H.L., Fang, J.K.H., Carreiro-Silva, M., Tribollet, A. and Wisshak, M. (2017b) Bioerosion: the other ocean acidification problem. ICES Journal of Marine Science 74, 895925.CrossRefGoogle Scholar
Schönberg, C.H.L. and Ortiz, J. (2009) Is sponge bioerosion increasing? Proceedings of the 11th International Coral Reef Symposium, Fort Lauderdale, Florida, 7–11 July 2008, Volume 1, pp. 520523.Google Scholar
Soekarno, R. (1989) Comparative studies on the status of Indonesian coral reefs. Netherlands Journal of Sea Research 23, 215222.CrossRefGoogle Scholar
Tadjuddah, M., Mustafa, A., Pangerang, U.K. and Yasidi, F. (2012) Application of satellite multi-sensor techniques to detect upwellings and potential fishing grounds in Wakatobi Marine National Park, Southeast Sulawesi, Indonesia. Aquatic Ecosystem Health & Management 15, 303310.CrossRefGoogle Scholar
Tribollet, A., Decherf, G., Hutchings, P. and Peyrot-Clausade, M. (2002) Large-scale spatial variability in bioerosion of experimental coral substrates on the Great Barrier Reef (Australia): importance of microborers. Coral Reefs 21, 424432.Google Scholar
Tribollet, A. and Golubic, S. (2005) Cross-shelf differences in the pattern and pace of bioerosion of experimental carbonate substrates exposed for 3 years on the northern Great Barrier Reef, Australia. Coral Reefs 24, 422434.CrossRefGoogle Scholar
Wisshak, M. and Tapanila, L. (2008) Current developments in bioerosion. Berlin: Springer.CrossRefGoogle Scholar
Wyrtki, K. (1961) Physical oceanography of the Southeast Asian Waters. NAGA report volume 2. San Diego, CA: Scripps Institution of Oceanography, 195 pp.Google Scholar
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