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Hydrobiologia

, Volume 691, Issue 1, pp 239–253 | Cite as

Sensitivity of dissolved organic carbon exchange and sediment bacteria to water quality in mangrove forests

  • María Fernanda Adame
  • Ruth Reef
  • Jorge A. Herrera-Silveira
  • Catherine E. Lovelock
Primary Research Paper

Abstract

Poor water quality affects the biogeochemistry functions and the biological community structure of coastal ecosystems. In this study we investigated the effect of water quality on: (a) The exchange of dissolved organic carbon (DOC) between floodwater and mangrove forests, (b) the abundance of sediment bacteria, (c) the microbial community composition, and (d) the microbial catabolic activity. We selected six mangrove forests that were flooded by creeks with differing water qualities to test for thresholds of nutrient concentrations associated with changes in DOC dynamics and the microbial community. Our results show that in sites flooded by water high in soluble reactive phosphorus (SRP) (>20 μg l−1) and NH4 + (>30 μg l−1) the DOC concentrations in the floodwater were higher than in ebb water, suggesting DOC import by the mangroves. In contrast, in sites flooded by water low in SRP (<20 μg l−1) and NH4 + (<30 μg l−1), DOC concentrations in the floodwater were lower than in the ebb water, suggesting DOC export by the mangroves. Bacterial abundance was higher in sediments with low bulk density, high organic carbon and when flooded by water with low N:P (1–2), but the microbial composition and total catabolic activity assessed using Biolog Ecoplates™ did not differ among sites. The relationship between water quality, microbial communities and DOC exchange suggests that, at least during some periods of the year, poor water quality increases bacterial abundance and modifies DOC exchange of mangrove forests with floodwater and thus, their role in supporting near-shore productivity.

Keywords

Nutrients Wetlands Eutrophication Phosphorus Moreton Bay Avicennia marina 

Notes

Acknowledgments

We thank the Mexican Council for Science and Technology (CONACYT, Mexico), The School of Biological Sciences at The University of Queensland and CINVESTAV-IPN (Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional), Unidad Mérida for financial and logistic support. We also want to acknowledge Dr. Aldrie Amir, Dr. Alistar Grinham, Dr. Jock Mackenzie, and Dr. Esteban Marcellin for field assistance and Dr. Timothy Mercer for field and editing assistance. This work was partially supported by ARC Linkage award LP0561498. I also like to thank the Queensland Environmental Protection Agency for giving access to data from their monitoring program. We appreciate the time and comments provided by two anonymous referees.

References

  1. Abal, E. G. & W. C. Dennison, 1999. Moreton Bay study: a scientific basis for the healthy waterways campaign. South East Queensland Regional Water Quality Management Strategy, Brisbane, Australia.Google Scholar
  2. Adame, M. F. & C. E. Lovelock, 2010. Carbon and nutrient exchange of mangrove forests with the coastal ocean. Hydrobiologia 663: 23–50.CrossRefGoogle Scholar
  3. Adame, M. F., D. Virdis & C. E. Lovelock, 2010. Effect of rainfall and geomorphological setting in nutrient exchange in mangroves during tidal inundation. Marine and Freshwater Research 61: 1197–1206.CrossRefGoogle Scholar
  4. Alongi, D. M., 1988. Bacterial productivity and microbial biomass in tropical mangrove sediments. Microbial Ecology 15: 59–79.CrossRefGoogle Scholar
  5. Alongi, D. M., 1991. The role of intertidal mudbanks in the diagenesis and export of dissolved and particulate materials from the Fly Delta, Papua New Guinea. Journal of Experimental Biology and Ecology 149: 81–107.CrossRefGoogle Scholar
  6. Alongi, D. M., 1994. The role of bacteria in nutrient recycling in tropical mangrove and other coastal benthic ecosystems. Hydrobiologia 285: 19–32.CrossRefGoogle Scholar
  7. Alongi, D. M. & A. D. McKinnon, 2005. The cycling and fate of terrestrially-derived sediments and nutrients in the coastal zone of the Great Barrier Reef shelf. Marine Pollution Bulletin 51: 239–252.PubMedCrossRefGoogle Scholar
  8. Alongi, D. M., P. Christoffersen & F. Tirendi, 1993. The influence of forest type on microbial–nutrient relationships in tropical mangrove sediments. Journal of Experimental Biology and Ecology 171: 201–223.CrossRefGoogle Scholar
  9. Alongi, D. M., V. C. Chong, P. Dixon, A. Sasekumar & F. Tirendi, 2003. The influence of fish cage aquaculture on pelagic carbon flow and water chemistry in tidally dominated mangrove estuaries of peninsular Malaysia. Marine Environmental Research 55: 313–333.PubMedCrossRefGoogle Scholar
  10. Al-Sayed, H. A., E. H. Ghanem & K. M. Saleh, 2005. Bacterial community and some physico-chemical characteristics in a subtropical mangrove environment in Bahrain. Marine Pollution Bulletin 50: 147–155.PubMedCrossRefGoogle Scholar
  11. ANZECC, Australian and New Zealand Environment and Conservation Council and Agriculture and Resource Management Council of Australia and New Zealand, 2000. An introduction to the Australian and New Zealand Guidelines for fresh and marine water quality. National Water quality management strategy. No. 4a. Australia.Google Scholar
  12. Ashokkumar, S., G. Rajaram, P. Manivasagan, S. Ramesh, P. Sampathkumar & P. Mayavu, 2011. Studies on hydrographical parameters, nutrients and microbial populations of Mullipallam, Creek in Muthupettai mangroves (southeast coast of India). Research Journal of Microbiology 6: 71–86.CrossRefGoogle Scholar
  13. Australian Bureau of Meteorology, Australian Government. www.bom.gov.au/.
  14. Bano, N., M.-U. Nisa, N. Khan, M. Saleem, P. J. Harrison, S. I. Ahmed & F. Azam, 1997. Significance of bacteria in the flux of organic matter in the tidal creeds of the mangrove ecosystem of the Indus River delta, Pakistan. Marine Ecology Progress Series 157: 1–12.CrossRefGoogle Scholar
  15. Benner, R., E. Peele & R. Hodson, 1986. Microbial utilization of dissolved organic matter from leaves of the red mangrove, Rhizophora mangle, in the Fresh Creek Estuary, Bahamas. Estuarine, Coastal and Shelf Science 23: 607–619.CrossRefGoogle Scholar
  16. Boto, K. G., D. M. Alongi & A. L. J. Nott, 1989. Dissolved organic carbon–bacteria interactions at sediment-water interface in a tropical mangrove system. Marine Ecology Progress Series 51: 243–251.CrossRefGoogle Scholar
  17. Bouillon, S., M. Frankignoulle, F. Dehairs, B. Velimirov, A. Eiler, G. Abril, H. Etcheber & A. Vieira Borges, 2003. Inorganic and organic carbon biogeochemistry in the Gautami Godavari estuary (Andhra Pradesh, India) during pre-monsoon: the local impact of extensive mangrove forests. Global Biogeochemical Cycles 17: 1114.Google Scholar
  18. Caron, D. A., 1994. Inorganic nutrients, bacteria, and the microbial loop. Microbial Ecology 28: 295–298.CrossRefGoogle Scholar
  19. Cloern, J. E., 2001. Our evolving conceptual model of the coastal eutrophication model. Marine Ecology Progress Series 210: 223–253.CrossRefGoogle Scholar
  20. Cotner, J. B. Jr. & R. G. Wetzel, 1992. Uptake of dissolved inorganic and organic phosphorus compounds by phytoplankton and bacterioplankton. Limnology and Oceanography 37: 232–243.CrossRefGoogle Scholar
  21. Díaz, R. J. & R. Rosenberg, 1995. Marine benthic hypoxia: a review of its ecological effects and the behavioral responses of benthic macrofauna. Oceanography and Marine Biology Annual Review 33: 245–303.Google Scholar
  22. Dittmar, T. & R. J. Lara, 2001. Do mangroves rather than rivers provide nutrients to coastal environments south of the Amazon River? Evidence from long-term flux measurements. Marine Ecology Progress Series 213: 67–77.CrossRefGoogle Scholar
  23. Duke, N. C., 2006. Australia’s Mangroves. The authoritative guide to Australia’s mangrove plants. University of Queensland, Brisbane.Google Scholar
  24. Eyre, B. D. & L. J. McKee, 2002. Carbon, nitrogen, and phosphorus budgets for a shallow subtropical coastal embayment (Moreton Bay, Australia). Limnology and Oceanography 47: 1043–1055.CrossRefGoogle Scholar
  25. Feller, I., 1995. Effects of nutrient enrichment on growth and herbivory of dwarf mangrove (Rhizophora mangle). Ecology Monographs 65: 477–505.CrossRefGoogle Scholar
  26. Gonzalez-Acosta, B., Y. Bashan, N. Y. Herandez-Saavedra, F. Ascencio & G. De la Cruz-Agüero, 2005. Seasonal seawater temperature as the major determinant for populations of culturable bacteria in the sediments of an intact mangrove in an arid region. FEMS Microbiology Ecology 55: 311–321.CrossRefGoogle Scholar
  27. Heiri, O., A. F. Lotter & G. Lemcke, 2001. Loss on ignition as a method for estimating organic and carbonate content in sediments: reproducibility and comparability of results. Journal of Paleolimnology 25: 101–110.CrossRefGoogle Scholar
  28. Holguin, G., P. Vazquez & Y. Bashan, 2001. The role of sediment microorganisms in the productivity, conservation, and rehabilitation of mangrove ecosystems: an overview. Biology and Fertility of Soils 33: 265–278.CrossRefGoogle Scholar
  29. Holmes, R. M., A. Aminot, R. Kérouel, B. A. Hooker & B. J. Peterson, 1999. A simple and precise method for measuring ammonium in marine and freshwater ecosystems. Canadian Journal of Fisheries and Aquatic Sciences 56: 1801–1808.Google Scholar
  30. Huiluo, C., M. Li, Y. Hong & J.-D. Gu, 2011. Diversity and abundance of ammonia-oxidizing archaea and bacteria in polluted mangrove sediment. Systematic and applied microbiology 34: 513–523.CrossRefGoogle Scholar
  31. Jørgensen, B. B., 1996. Eutrophication in coastal marine ecosystems. American Geophysical Union, New York: 243 pp.CrossRefGoogle Scholar
  32. Karydis, M., 1995. Quantitative assessment of eutrophication: a scoring system for characterizing water quality in coastal marine ecosystems. Environmental Monitoring and Assessment 41: 233–246.CrossRefGoogle Scholar
  33. Kirchmann, D. L., 1990. Limitation of bacterial growth by dissolved organic matter in the subarctic Pacific. Marine Ecology Progress Series 62: 47–54.CrossRefGoogle Scholar
  34. Kirchmann, D. L., 1994. The uptake of inorganic nutrients by heterotrophic bacteria. Microbial Ecology 28: 255–271.CrossRefGoogle Scholar
  35. Lapointe, B. E., 1997. Nutrient thresholds for bottom-up control of macroalgal blooms on coral reefs in Jamaica and southeast Florida. Limnology and Oceanography 45: 1119–1131.CrossRefGoogle Scholar
  36. Lebo, M. E., 1990. Phosphate uptake along a coastal plain estuary. Limnology and Oceangraphy 35: 1279–1289.CrossRefGoogle Scholar
  37. Lee, R., P. William, I. Feller, K. McKee & S. Joye, 2008. Porewater biogeochemistry and soil metabolism in dwarf red mangrove habitats (Twin Cays, Belize). Biogeochemistry 87: 181–198.CrossRefGoogle Scholar
  38. Lotze, H. K., H. S. Lenihan, B. J. Bourque, R. H. Bradbury, R. G. Cooke, M. C. Kay, S. M. Kidwell, M. X. Kirby, C. H. Peterson & J. B. C. Jackson, 2006. Depletion, degradation and recovery potential of estuaries and coastal oceans. Science 312: 1806–1809.PubMedCrossRefGoogle Scholar
  39. Lovelock, C. E., M. C. Ball, K. C. Martin & I. C. Feller, 2009. Nutrient enrichment increases mortality of mangroves. PLoS ONE 4(5): e5600.PubMedCrossRefGoogle Scholar
  40. Machiwa, J. F. & R. O. Hallberg, 2002. An empirical model of the fate of organic carbon in a mangrove forest partly affected by anthropogenic activity. Ecological Modeling 147: 69–83.CrossRefGoogle Scholar
  41. Marchand, C., P. Albéric, E. Lallier-Vergès & F. Baltzer, 2006. Distribution and characteristics of dissolved organic matter in mangrove sediment pore waters along the coastline of French Guiana. Biogeochemistry 81: 59–75.CrossRefGoogle Scholar
  42. McKee, K. L., 1993. Soil physicochemical patterns and mangrove species distribution—reciprocal effects. Journal of Ecology 81: 477–487.CrossRefGoogle Scholar
  43. McKee, K., D. Cahoon & I. Feller, 2007. Caribbean mangroves adjust to rising sea level through biotic controls on change in soil elevation. Global Ecology and Biogeography Letters 16: 545–556.CrossRefGoogle Scholar
  44. Melville, F. & A. Pulkownik, 2006. Investigation of mangrove macroalgae as bioindicators of estuarine contamination. Marine Pollution Bulletin 52: 1260–1269.PubMedCrossRefGoogle Scholar
  45. Murrell, M. C. & E. M. Lores, 2004. Phytoplankton and zooplankton seasonal dynamics in a subtropical estuary: importance of cyanobacteria. Journal of Plankton Research 26: 371–382.CrossRefGoogle Scholar
  46. Nixon, S. W., 1995. Coastal marine eutrophication: a definition, social causes and future concerns. Ophelia 41: 199–219.Google Scholar
  47. Nixon, S. W., C. A. Oviatt, J. Frithsen & B. Sullivan, 1986. Nutrients and the productivity of estuarine and coastal marine ecosystems. Journal of the Limnological Society of South Africa 12: 43–71.CrossRefGoogle Scholar
  48. Officer, C. B., T. J. Smayda & R. Mann, 1982. Benthic filter feeding: a natural eutrophication control. Marine Ecology Progress Series 9: 203–210.CrossRefGoogle Scholar
  49. Onuf, C. P., J. M. Teal & I. Valiela, 1977. Interactions of nutrients, plant growth and herbivory in a mangrove ecosystem. Ecology 58: 514–526.CrossRefGoogle Scholar
  50. OzCoast Australian Online Coastal Information. Geoscience, Australian. Australian Government. http://www.ozcoasts.gov.au/.
  51. Paerl, H. W., J. Dyble, P. H. Moisander, R. T. Noble, M. F. Piehler, J. L. Pinckney, T. F. Steppe, L. Twomey & L. M. Valeds, 2003. Microbial indicators of aquatic ecosystem change: current applications to eutrophication studies. FEMS Microbiology Ecology 46: 233–246.PubMedCrossRefGoogle Scholar
  52. Pejrup, M., 1988. Suspended sediment transport across a tidal flat. Marine Geology 82: 187–198.CrossRefGoogle Scholar
  53. Pregnall, A. M., 1983. Release of dissolved organic carbon from the estuarine intertidal macroalga Enteromorpha prolifera. Marine Biology 73: 37–42.CrossRefGoogle Scholar
  54. Ridd, P., R. Sam, S. Hollins & G. J. Brunskill, 1997. Water, salt and nutrient fluxes of tropical tidal salt flats. Mangroves and Salt Marshes 1: 229–238.CrossRefGoogle Scholar
  55. Roman, C. & F. Daiber, 1989. Organic flux through a Delaware Bay salt marsh: tidal exchange, particle size distribution and storms. Marine Ecology Progress Series 54: 149–156.CrossRefGoogle Scholar
  56. Southeast Queensland Healthy waterways, Australia. www.healthywaterways.org/.
  57. Tam, N. F., 1998. Effects of wastewater discharge on microbial populations and enzyme activities in mangrove soils. Environmental Pollution 102: 233–242.CrossRefGoogle Scholar
  58. Twilley, R. R., 1985. The exchange of organic carbon in basin mangrove forests in a southwest Florida estuary. Estuarine, Coastal and Shelf Science 20: 543–557.CrossRefGoogle Scholar
  59. Valiela, I. & M. L. Cole, 2002. Comparative evidence that salt marshes and mangroves may protect seagrass meadow from land-derived nitrogen loads. Ecosystems 5: 92–102.CrossRefGoogle Scholar
  60. Valiela, I., J. McCLelland, J. Hauxwell, P. J. Behr, D. Hersh & K. Foremean, 1997. Macroalgal blooms in shallow estuaries: controls and ecophysiological and ecosystem consequences. Limnology and Oceanography 42: 1105–1118.CrossRefGoogle Scholar
  61. Verhoven, J. T. A., B. Arheimer, Y. Chengqing & M. Hefting, 2006. Regional and global concerns over wetlands and water quality. Trends in Ecology and Evolution 21: 96–103.CrossRefGoogle Scholar
  62. Vymazal, J., 1995. Algae and element cycling in wetlands. Lewis Publishers, Boca Raton.Google Scholar
  63. Wang, M., J. Zhang, Z. Tu, X. Gao & W. Wang, 2010. Maintenance of estuarine water quality by mangroves occurs during flood periods: a case study of a subtropical mangrove wetland. Marine Pollution Bulletin 60: 2154–2160.PubMedCrossRefGoogle Scholar
  64. Wickramasinghe, S., M. Borin, S. W. Kotagama, R. Cochard, A. J. Anceno & O. V. Shipin, 2008. Multi-functional pollution mitigation in a rehabilitated mangrove conservation area. Ecological engineering 35: 898–907.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2012

Authors and Affiliations

  • María Fernanda Adame
    • 1
    • 2
  • Ruth Reef
    • 1
  • Jorge A. Herrera-Silveira
    • 2
  • Catherine E. Lovelock
    • 1
  1. 1.School of Biological SciencesThe University of QueenslandSt LuciaAustralia
  2. 2.Centro de Investigación y de Estudios Avanzados (CINVESTAV) del I.P.N., Unidad MéridaMéridaMexico

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