Skip to main content

Trace metal concentrations in the tropical sponge Spheciospongia vagabunda at a sewage outfall: synchrotron X-ray imaging reveals the micron-scale distribution of accumulated metals

  • SPONGE RESEARCH DEVELOPMENTS
  • Chapter
  • First Online:
Ancient Animals, New Challenges

Part of the book series: Developments in Hydrobiology ((DIHY,volume 219))

  • 742 Accesses

Abstract

Major and trace elements were measured in sponges, seawater and sediment in Darwin Harbour (Australia) to test the hypothesis that metals are elevated in sponges closer to a sewage outfall compared with unimpacted sites. Seawater and sediment at the sewage discharge site contained high, but localised, concentrations of phosphorus (P), manganese (Mn), iron (Fe), cobalt (Co), nickel (Ni), copper (Cu), zinc (Zn), arsenic (As) and lead (Pb) compared with background sites. Metal concentrations in the sponge Spheciospongia vagabunda were highly elevated compared with other sponges and, although site specific, high metal concentrations were unrelated to the presence of sewage effluent. X-ray fluorescence microprobe imaging was used to investigate the metal distribution pattern in S. vagabunda. High Fe, Ni and Zn concentrations were either localised in circular patches (100–200 μm size) near water canals or in the pinacoderm, or scattered in spots (approximately 10 μm) throughout the tissue. This supports a microflora-mediated metal bioaccumulation hypothesis. In contrast, Co and Mn were highly dispersed and probably associated with aluminium- and iron-oxide rich sediment inclusions. Although the lack of association between sewage effluent and metal accumulation precludes the use of S. vagabunda as a biomonitor, the apparent differential mechanisms of metal accumulation warrants further investigation.

Guest editors: M. Maldonado, X. Turon, M. A. Becerro & M. J. Uriz / Ancient animals, new challenges: developments in sponge research

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Aguiar, P., J. Medeiros, A. Costa, M. Humanes & M. Barreto, 2010. Distribution of nickel in the tissue of Cliona viridis from the coast of São Miguel (Azores). VIII World Sponge Conference, Girona, Spain.

    Google Scholar 

  • Anderson, M. J., R. N. Gorley & K. R. Clarke, 2008. PERMANOVA+ for PRIMER: Guide to Software and Statistical Methods. PRIMER-E Ltd, Plymouth, UK.

    Google Scholar 

  • ANZECC, 2000. Australian and New Zealand Guidelines for Fresh and Marine Water Quality. ANZECC, Australia.

    Google Scholar 

  • Araújo, M., A. Cruz, M. Humanes, M. Lopes, J. A. L. da Silva & J. J. R. da Silva, 1999. Elemental composition of Demospongiae from the eastern Atlantic coastal waters. Chemical Speciation and Bioavailability 11: 25–36.

    Article  Google Scholar 

  • Araújo, M., A. Conceição, T. Barbosa, M. Lopes & M. Humanes, 2003. Elemental composition of marine sponges from the Berlengas natural park, western Portuguese coast. X-Ray Spectrometry 32: 428–433.

    Article  Google Scholar 

  • Australian Synchrotron, 2010. Australian Synchrotron Technical Information (XFM). Australian Synchrotron [available on internet at http://www.synchrotron.org.au/index.php/aussyncbeamlines/x-ray-fluorescence-microprobe-x-ray-microspectroscopy/technical-information].

  • Bargagli, R., L. Nelli, S. Ancora & S. Focardi, 1996. Elevated cadmium accumulation in marine organisms from Terra Nova Bay (Antarctica). Polar Biology 16: 513–520.

    Article  Google Scholar 

  • Becerro, M., X. Turon & M. J. Uriz, 1997. Multiple functions for secondary metabolites in encrusting marine invertebrates. Journal of Chemical Ecology 23: 1527–1547.

    Article  CAS  Google Scholar 

  • Bowen, V. & D. Sutton, 1951. Comparative studies of mineral constituents of marine sponges I. The genera Dysidea, Chondrilla, Terpios. Journal of Marine Research X: 153–167.

    Google Scholar 

  • Capon, R., K. Elsbury, M. Butler, C. Lu, J. Hooper, J. Rostas, K. O’Brien, L. Mudge & A. Sim, 1993. Extraordinary levels of cadmium and zinc in a marine sponge, Tedania charcoti Topsent: inorganic chemical defense agents. Cellular and Molecular Life Sciences 49: 263–264.

    Article  CAS  Google Scholar 

  • Cebrian, E., M. Uriz & X. Turon, 2007. Sponges as biomonitors of heavy metals in spatial and temporal surveys in northwestern Mediterranean: multispecies comparison. Environmental Toxicology and Chemistry 26: 2430–2439.

    Article  CAS  Google Scholar 

  • Cox, G. & A. Larkum, 1983. A diatom apparently living in symbiosis with a sponge. Bulletin of Marine Science 33: 943–945.

    Google Scholar 

  • CSIRO, 2010. Quantitative Imaging Using Dynamic Analysis. CSIRO [available on internet at http://nmp.csiro.au/dynamic.html].

  • Denton, G., L. Concepcion, H. Wood, V. Eflin & G. Pangelinan, 1999. Heavy Metals, PCBs and PAHs in Marine Organisms from Four Harbor Locations on Guam. Technical Report No. 87. Water and Environmental Research Institute of the Western Pacific University of Guam.

    Google Scholar 

  • Dettrick, D. & K. Schlusser, 2006. A Report on Larrakeyah Sewage Outfall, Darwin Harbour, August 2006. Northern Territory Government: 1–17.

    Google Scholar 

  • Esteves, A., S. Chaves, J. Xavier, R. Tenreiro & M. Humanes, 2010. A new Symbiodinium sp. lineage in Atlanto-Mediterranean Cliona viridis. VIII World Sponge Conference, Girona, Spain.

    Google Scholar 

  • Flowers, A., M. Garson, R. Webb, E. Dumdei & R. Charan, 1998. Cellular origin of chlorinated diketopiperazines in the dictyoceratid sponge Dysidea herbacea (Keller). Cell and Tissue Research 292: 597–607.

    Article  CAS  Google Scholar 

  • Fortune, J., 2006. The Grainsize and Heavy Metal Content of Sediment in Darwin Harbour. Report No. 14/2006D. Aquatic Health Unit (Northern Territory Government) and the Environment Protection Agency.

    Google Scholar 

  • Garson, M., J. Thompson, R. M. Larsen, C. H. Battershill, P. T. Murphy & P. R. Bergquist, 1992. Terpenes in sponge cell membranes: cell separation and membrane fractionation studies with the tropical marine sponge Amphimedon sp. Lipids 27: 378–388.

    Article  CAS  Google Scholar 

  • Garson, M., A. Flowers, R. Webb, R. Charan & E. J. McCaffrey, 1998. A sponge/dinoflagellate association in the haplosclerid sponge Haliclona sp.: cellular origin of cytotoxic alkaloids by Percoll density gradient fractionation. Cell and Tissue Research 293: 365–373.

    Article  CAS  Google Scholar 

  • Hansen, I., J. Weeks & M. Depledge, 1995. Accumulation of copper, zinc, cadmium and chromium by the marine sponge Halichondria panicea Pallas and the implications for biomonitoring. Marine Pollution Bulletin 31: 133–138.

    Article  CAS  Google Scholar 

  • Hentschel, U., J. Hopke, M. Horn, A. Friedrich, M. Wagner, J. Hacker & B. Moore, 2002. Molecular evidence for a uniform microbial community in sponges from different oceans. Applied and Environmental Microbiology 68: 4431–4440.

    Article  CAS  Google Scholar 

  • Holmes, B. & H. Blanch, 2007. Genus-specific associations of marine sponges with group I crenarchaeotes. Marine Biology 150: 759–772.

    Article  Google Scholar 

  • Kelly-Borges, M. & J. Vacelet, 1998. Sponges of the New Caledonian Lagoon: class Demospongiae, order Hadromerida. In Levi, C. (ed.), Sponges of the New Caledonian Lagoon. Orstom Editions, Paris: 87–93.

    Google Scholar 

  • Long, E., D. MacDonald, S. Smith & F. Calder, 1995. Incidence of adverse biological effects within ranges of chemical concentrations in marine and estuarine sediments. Environmental Management 19: 81–97.

    Article  Google Scholar 

  • Moir, C. M., 1995. The effects of sewage discharge on the water quality of Darwin Harbour and Buffalo Creek. Northern Territory University Honours thesis.

    Google Scholar 

  • Munksgaard, N. & D. Parry, 2001. Trace metals, arsenic and lead isotopes in dissolved and particulate phases of North Australian coastal and estuarine seawater. Marine Chemistry 75: 165–184.

    Article  CAS  Google Scholar 

  • Munksgaard, N. & D. Parry, 2002. Metals, arsenic and lead isotopes in near-pristine estuarine and marine coastal sediments from northern Australia. Marine & Freshwater Research 53: 719–729.

    Article  CAS  Google Scholar 

  • Negri, A., K. Burns, S. Boyle, D. Brinkman & N. Webster, 2006. Contamination in sediments, bivalves and sponges of McMurdo Sound, Antarctica. Environmental Pollution 143: 456–467.

    Article  CAS  Google Scholar 

  • Olesen, T. & J. Weeks, 1994. Accumulation of Cd by the marine sponge Halichondria panicea Pallas: effects upon filtration rate and its relevance for biomonitoring. Bulletin of Environmental Contamination and Toxicology 52: 722–728.

    Article  CAS  Google Scholar 

  • Padovan, A., 2002. Darwin Harbour Water Quality Monitoring 2001/02 Report. Report No. 23/2002. Water Monitoring Section, Natural Resource Management Division, Conservation and Natural Resources Group: 1–16.

    Google Scholar 

  • Padovan, A., 2003. Darwin Harbour water and sediment quality. Proceedings of the Darwin Harbour Public Presentations, February 2003, Darwin, NT, Australia: 5–18.

    Google Scholar 

  • Patel, B., M. Balani & S. Patel, 1985. Sponge ‘sentinel’ of heavy metals. The Science of the Total Environment 41: 145–152.

    Article  Google Scholar 

  • Perez, T., D. Longet, T. Schembri, P. Rebouillon & J. Vacelet, 2005. Effects of 12 years’ operation of a sewage treatment plant on trace metal occurrence within a Mediterranean commercial sponge (Spongia officinalis, Demospongiae). Marine Pollution Bulletin 50: 301–309.

    Article  CAS  Google Scholar 

  • Philp, R., 1999. Cadmium content of the marine sponge Microciona prolifera, other sponges, water and sediment from the eastern Florida panhandle: possible effects on Microciona cell aggregation and potential roles of low pH and low salinity. Comparative Biochemistry and Physiology Part C 124: 41–49.

    Article  CAS  Google Scholar 

  • Philp, R., F. Leung & C. Bradley, 2003. A comparison of the metal content of some benthic species from coastal waters of the Florida Panhandle using high-resolution inductively coupled plasma mass spectrometry (ICP-MS) analysis. Archives of Environmental Contamination and Toxicology 44: 218–223.

    Article  CAS  Google Scholar 

  • Power and Water Corporation, 2006. Wastewater Treatment, Reuse and Discharge Report 2006. Power and Water Corporation.

    Google Scholar 

  • Preston, C., K. Wu, T. Molinski & E. DeLong, 1996. A psychrophilic crenarchaeon inhabits a marine sponge: Cenarchaeum symbiosum gen. nov., sp. nov. Proceedings of the National Academy of Sciences of the United States of America 93: 6241–6246.

    Article  CAS  Google Scholar 

  • Quinn, G. & M. Keough, 2002. Experimental Design and Data Analysis for Biologists. Cambridge University Press, Cambridge, UK.

    Book  Google Scholar 

  • Rao, J., P. Kavitha, N. Reddy & T. Rao, 2006. Petrosia testudinaria as a biomarker for metal contamination at Gulf of Mannar, southeast coast of India. Chemosphere 6: 634–638.

    Article  Google Scholar 

  • Rao, J. V., K. Srikanth, R. Pallela & T. G. Rao, 2009. The use of marine sponge, Haliclona tenuiramosa as bioindicator to monitor heavy metal pollution in the coasts of Gulf of Mannar, India. Environmental Monitoring and Assessment 156: 451–459.

    Article  Google Scholar 

  • Reichelt-Brushett, A. J. & G. McOrist, 2003. Trace metals in the living and nonliving components of scleractinian corals. Marine Pollution Bulletin 46: 1573–1582.

    Article  CAS  Google Scholar 

  • Reiswig, H., 1971. Particle feeding in natural populations of three marine demosponges. Biological Bulletin 141: 568–591.

    Article  Google Scholar 

  • Ridley, S. O., 1884. Spongiida. In Report on the Zoological Collections made in the Indo-Pacific Ocean During the Voyage of H.M.S. ‘Alert’, 1881-2. British Museum of Natural History, London: 366–482, 339–343, 582–630, 353–354.

    Google Scholar 

  • Rützler, K., 1990. Associations between Caribbean sponges and photosynthetic organisms. In Rützler, K. (ed.), New Perspectives in Sponge Biology. Smithsonian Institution Press, Washington, DC: 455–466.

    Google Scholar 

  • Rützler, K., 1997. The role of psammobiontic sponges in the reef community. Proceedings of the 8th International Coral Reef Symposium, Vol. 2: 1393–1397.

    Google Scholar 

  • Ryan, C. G., 2000. Quantitative trace element imaging using PIXE and the nuclear microprobe. International Journal of Imaging Systems and Technology 11: 219–230.

    Article  Google Scholar 

  • Ryan, C. G., R. Kirkham, R. M. Hough, G. Moorhead, D. P. Siddons, M. D. de Jonge, D. J. Paterson, G. De Geronimo, D. L. Howard & J. S. Cleverley, 2010. Elemental X-ray imaging using the Maia detector array: the benefits and challenges of large solid-angle. Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 619: 37–43.

    Article  CAS  Google Scholar 

  • Sará, M. & L. Liaci, 1964. Symbiotic association between zooxanthellae and two marine sponges of the genus Cliona. Nature 203: 321.

    Article  Google Scholar 

  • Shah, S., 2008. Study of heavy metal accumulation in scleractinian corals of Viti Levu, Fiji Islands. University of the South Pacific Masters thesis.

    Google Scholar 

  • Skinner, L., S. Townsend & J. Fortune, 2009. The Impact of Urban Land-Use on Total Pollutant Loads Entering Darwin Harbour. Report 06/2008D. Aquatic Health Unit, Department of Natural Resources, Environment, the Arts and Sport, Northern Territory Government: 1–66.

    Google Scholar 

  • Sutcliffe, P. R., J. N. A. Hooper & C. R. Pitcher, 2010. The most common sponges on the Great Barrer Reef seabed, Australia, include species new to science (Phylum Porifera). Zootaxa 2616: 1–30.

    Google Scholar 

  • Turon, X., M. Becerro & M. Uriz, 2000. Distribution of brominated compounds within the sponge Aplysina aerophoba: coupling of X-ray microanalysis with cryofixation techniques. Cell and Tissue Research 301: 311–322.

    Article  CAS  Google Scholar 

  • Vacelet, J. & C. Donadey, 1977. Electron microscope study of the association between some sponges and bacteria. Journal of Experimental Marine Biology and Ecology 30: 301–314.

    Article  Google Scholar 

  • Vacelet, J., B. Verdenal & G. Perinet, 1988. The iron mineralization of Spongia officinalis L. (Porifera, Dictyoceratida) and its relationships with the collagen skeleton. Biology of the Cell 62: 189–198.

    CAS  Google Scholar 

  • Verdenal, B., C. Diana, A. Arnoux & J. Vacelet, 1985. Pollutant levels in Mediterranean commercial sponges. In Rützler, K. (ed.), Proceedings of the 3rd International Sponge Conference. Smithsonian Institution Press, Washington, DC: 516–524.

    Google Scholar 

  • Welch, M., J. Schult & A. J. Padovan, 2008. Effects of Urban Stormwater on Heavy Metal and Nutrient Concentrations in Mangrove Sediments of Darwin Harbour. Aquatic Health Unit, Department of Natural Resources, Environment, the Arts and Sport, Northern Territory Government Report 08/2008D: 1–37.

    Google Scholar 

  • Wilkinson, C. R., 1980. Cyanobacteria symbiotic in marine sponges. In Schwemmler, W. & H. E. A. Schenk (eds), Endocytobiology. Walter de Gruyter, Berlin: 553–563.

    Google Scholar 

  • Woods, B. B., 1998. Heavy metals in Darwin Harbour sediments and the use of lead isotope ratios for the determination of anthropogenic sources of lead. Northern Territory University Honours thesis.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Anna Padovan .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2011 Springer Science+Business Media B.V.

About this chapter

Cite this chapter

Padovan, A., Munksgaard, N., Alvarez, B., McGuinness, K., Parry, D., Gibb, K. (2011). Trace metal concentrations in the tropical sponge Spheciospongia vagabunda at a sewage outfall: synchrotron X-ray imaging reveals the micron-scale distribution of accumulated metals. In: Maldonado, M., Turon, X., Becerro, M., Jesús Uriz, M. (eds) Ancient Animals, New Challenges. Developments in Hydrobiology, vol 219. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-4688-6_23

Download citation

Publish with us

Policies and ethics