Skip to main content

Dynamics of a benthic microbial community in a riverine environment subject to hydrological fluctuations (Mulargia River, Italy)

  • Global Change and River Ecosystems
  • Chapter
Global Change and River Ecosystems—Implications for Structure, Function and Ecosystem Services

Part of the book series: Developments in Hydrobiology 215 ((DIHY,volume 215))

  • 1221 Accesses

Abstract

Temporary rivers are characterized by recurrent dry phases, and global warming will stress their hydrology by amplifying extreme events. Microbial degradation and transformation of organic matter (OM) in riverbed sediment are key processes with regard to carbon and nutrient fluxes. In this study, we describe structural and functional changes of benthic microbial communities in a riverine environment subject to hydrological fluctuation. Sampling was carried out in the outlet section of the Mulargia River (Sardinia, Italy) under various water regimes, including one flood event. Overall, sediments were characterized by low bacterial cell abundance (range 0.6–1.8 × 109 cell g−1) as a consequence of their low nutrient and OM concentrations. No major differences were found in the community composition. Alpha-Proteobacteria dominated during the whole year (range 21–30%) followed by Beta-Proteobacteria, Gamma-Proteobacteria, and Cytophaga-Flavobacteria which always contributed <18%. Planctomycetes and Firmicutes were found in smaller amounts (<7%). In spring, when the highest total organic carbon content was also detected (0.42% w/w), both bacterial abundance and C production (BCP, 170 nmol C h−1 g−1) reached relatively high values. During the flood event, an increase in BCP and the highest values of community respiration (CR, 74 nmol C h−1 g−1) were observed. Moreover, most of the extracellular enzyme activities (EEA) changed significantly during the flood. The variation of the water flow itself can explain part of these changes and other factors also come into play. The presence of different patterns of functional parameters could suggest that the quality of the OM could be the major driving force in nutrient flux.

Guest editors: R. J. Stevenson, S. Sabater / Global Change and River Ecosystems – Implications for Structure, Function and Ecosystem Services

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.

Similar content being viewed by others

References

  • Allen, M. & W. I. Ingram, 2002. Constrains on future changes in climate and the hydrologic cycle. Nature 419: 224–232.

    Article  CAS  PubMed  Google Scholar 

  • Amalfitano, S. & S. Fazi, 2008. Recovery and quantification of bacterial cells associated with streambed sediments. Journal of Microbiological Methods 75: 237–243.

    Article  CAS  PubMed  Google Scholar 

  • Amalfitano, S., S. Fazi, A. Zoppini, A. Barra Caracciolo, P. Grenni & A. Puddu, 2008. Responses of benthic bacteria to experimental drying in sediments from Mediterranean temporary rivers. Microbial Ecology 55: 270–279.

    Article  CAS  PubMed  Google Scholar 

  • Bååth, E., M. Pettersson & K. Söderberg, 2001. Adaptation of a rapid an economical microcentrifugation method to measure thymidine and leucine incorporation by soil bacteria. Soil Biology and Biochemistry 33: 1571–1574.

    Article  Google Scholar 

  • Baldwin, D. S. & A. M. Mitchell, 2000. The effects of drying and reflooding on the sediment and soil nutrient dynamics of lowland river-floodplain systems: a synthesis. Regulated Rivers: Research and Management 16: 457–467.

    Article  Google Scholar 

  • Bastviken, D., M. Olsson & L. Tranvik, 2003. Simultaneous measurements of organic carbon mineralization and bacterial production in oxic and anoxic lake sediments. Microbial Ecology 46: 73–82.

    Article  CAS  PubMed  Google Scholar 

  • Battin, T. M., L. A. Kaplan, J. D. Newbold & C. M. E. Hansen, 2003. Contributions of microbial biofilms to ecosystem processes in stream mesocosms. Nature 426: 439–442.

    Article  CAS  PubMed  Google Scholar 

  • Bell, R. T. & I. Ahlgren, 1987. Thymidine incorporation and microbial respiration in the surface sediment of a hypereutrophic lake. Limnology and Oceanography 32: 476–482.

    Article  CAS  Google Scholar 

  • Bernal, S., A. Butturini, E. Nin, F. Sabater & S. Sabater, 2003. Leaf litter dynamics and nitrous oxide emission in a Mediterranean riparian forest. Journal of Environmental Quality 32: 191–197.

    Article  CAS  PubMed  Google Scholar 

  • Besemer, K., I. Hödl, G. Singe & T. J. Battin, 2009. Architectural differentiation reflects bacterial community structure in stream biofilms. International Society for Microbial Ecology Journal 3: 1318–1324.

    CAS  Google Scholar 

  • Brown, J. H., J. F. Gillooly, A. P. Allen, V. M. Savage & G. B. West, 2004. Towards a metabolic theory of ecology. Ecology 85: 1771–1789.

    Article  Google Scholar 

  • Buesing, N. & M. O. Gessner, 2003. Incorporation of radiolabeled leucine into protein to estimate bacterial production in plant litter sediment epiphytic biofilms and water samples. Microbial Ecology 45: 291–301.

    Article  CAS  PubMed  Google Scholar 

  • Buesing, N. & M. O. Gessner, 2006. Benthic bacterial and fungal productivity and carbon turnover in a freshwater marsh. Applied and Environmental Microbiology 72: 596–605.

    Article  CAS  PubMed  Google Scholar 

  • Buesing, N. & J. Marxsen, 2005. Theoretical and empirical conversion factors for determining bacterial production in freshwater sediments via leucine incorporation. Limnology and Oceanography 3: 101–107.

    CAS  Google Scholar 

  • Butturini, A., S. Bernal, C. Hellin, E. Nin, L. Rivero, S. Sabater & F. Sabater, 2003. Influences of the stream groundwater hydrology on nitrate concentration in unsaturated riparian area bounded by an intermittent Mediterranean stream. Water Resources Research 39: 1–13.

    Article  Google Scholar 

  • Chrost, R. J., 1991. Environmental control of the synthesis and activity of aquatic microbial ectoenzymes. In Chrost, R. J. (ed.), Microbial enzymes in aquatic environments. Springer-Verlag, New York: 29–59.

    Google Scholar 

  • Cole, J. J., Y. T. Prairie, N. F. Caraco, W. H. McDowell, L. J. Tranvik, R. G. Striegl, C. M. Duarte, P. Kortelainen, J. A. Downing, J. J. Middelburg & J. Melack, 2007. Plumbing the global carbon cycle: integrating inland waters into the terrestrial carbon budget. Ecosystems 10: 172–185.

    Article  Google Scholar 

  • Cunha, M. A., R. Pedro, M. A. Almeida & M. H. Silva, 2005. Activity and growth efficiency of heterotrophic bacteria in a salt marsh (Ria de Aveiro, Portugal). Microbiological Research 160: 279–290.

    Article  CAS  PubMed  Google Scholar 

  • Dahm, C. N., M. A. Baker, D. I. Moore & J. R. Thibault, 2003. Coupled biogeochemical and hydrological responses of streams and rivers to drought. Freshwater Biology 48: 1219–1231.

    Article  CAS  Google Scholar 

  • Del Giorgio, P. A. & J. J. Cole, 1998. Bacterial growth efficiency in natural aquatic systems. Annual Review of Ecology and Systematics 29: 503–541.

    Article  Google Scholar 

  • De Long, E. F., 2004. Microbial population genomics and ecology: the road ahead. Environmental Microbiology 6: 875–878.

    Article  Google Scholar 

  • den Heyer, C. & J. Kalfs, 1998. Organic matter mineralization rates in sediments: A within- and among-lake study. Limnology & Oceanography 43: 695–705.

    Article  Google Scholar 

  • Döring, M., 2007. Environmental heterogeneity and respiration in a dynamic river corridor: structural properties and functional performance. PhD Dissertation, University of Zurich, ETH No. 17046, pp. 1–137

    Google Scholar 

  • European Commission & Joint Research Centre, 2005. Climate change and the European Water dimension. In Eisenreich, S. J. (ed.), JRC, Ispra Italy: 253 pp

    Google Scholar 

  • Fazi, S., S. Amalfitano, J. Pernthaler & A. Puddu, 2005. Bacterial communities associated with benthic organic matter in headwater stream microhabitats. Environmental Microbiology 7: 1633–1640.

    Article  CAS  PubMed  Google Scholar 

  • Fazi, S., S. Amalfitano, C. Piccini, A. Zoppini, A. Puddu & J. Pernthaler, 2008. Colonization of overlaying water by bacteria from dry river sediments. Environmental Microbiology 10: 2760–2772.

    Article  CAS  PubMed  Google Scholar 

  • Findlay, S., J. Tank, S. Dye, H. M. Valett, P. J. Mulholland, W. H. McDowell, S. L. Johnson, S. K. Hamilton, J. Edmonds, W. K. Dodds & W. B. Bowden, 2002. A cross-system comparison of bacterial and fungal biomass in detritus pools of headwater streams. Microbial Ecology 43: 55–66.

    Article  CAS  PubMed  Google Scholar 

  • Findlay, S. E. G., R. L. Sinsabaugh, W. V. Sobczak & M. Hoostal, 2003. Metabolic and structural response of hyporheic microbial communities to variations in supply of dissolved organic matter. Limnology and Oceanography 48: 1608–1617.

    Article  CAS  Google Scholar 

  • Fischer, H. & M. Pusch, 2001. Comparison of bacterial production in sediments, epiphyton and the pelagic zone of a lowland river. Freshwater Biology 46: 1335–1348.

    Article  Google Scholar 

  • Fischer, H., A. Sachse, C. E. W. Steinberg & M. Pusch, 2002a. Differential retention and utilization of dissolved organic carbon by bacteria in river sediments. Limnology and Oceanography 47: 1702–1711.

    Article  Google Scholar 

  • Fischer, H., S. C. Wanner & M. Pusch, 2002b. Bacterial abundance and production in river sediments as related to the biochemical composition of particulate organic matter (POM). Biogeochemistry 61: 37–55.

    Article  CAS  Google Scholar 

  • Fonnesu, A., M. Pinna & A. Basset, 2004. Spatial and temporal variations of detritus breakdown rates in the river Flumendosa basin (Sardinia, Italy). International Review of Hydrobiology 89: 443–452.

    Article  Google Scholar 

  • Gallart, F., Y. Amaxidis, P. Botti, G. Canè, V. Castillo, P. Chapman, J. Froebrich, J. García-Pintado, J. Latron, P. Llorens, A. Lo Porto, M. Morais, R. Neves, P. Ninov, J. L. Perrin, I. Ribarova, N. Skoulikidis & M. G. Tournoud, 2008. Investigating hydrological regimes and processes in a set of catchments with temporary waters in Mediterranean Europe Hydrological Sciences. Journal des Sciences Hydrologiques 53: 618–628.

    Article  Google Scholar 

  • Gao, X., A. O. Olapade & L. G. Leff, 2005. Comparison of benthic bacterial community composition in nine streams. Aquatic Microbial Ecology 40: 51–60.

    Article  Google Scholar 

  • Gerakis, A. & B. Baer, 1999. A computer program for soil textural classification. Soil Science Society of America Journal 63: 807–808. http://nowlin.css.msu.edu/software/triangle_form.html/.

  • Gillooly, J. F., J. H. Brown, G. B. West, V. M. Savage & E. L. Charnov, 2001. Effects of size and temperature on metabolic rate. Science 293: 2248–2251.

    Article  CAS  PubMed  Google Scholar 

  • Glockner, F. O., B. M. Fuchs & R. Amann, 1999. Bacterioplankton compositions of lakes and oceans: A first comparison based on fluorescence in situ hybridization. Applied Environmental Microbiology 65: 3721–3726.

    CAS  Google Scholar 

  • Goedkoop, W., K. R. Gullberg, R. K. Johnson & I. Ahlgren, 1997. Microbial Response of a Freshwater Benthic Community to a Simulated Diatom Sedimentation Event: Interactive Effects of Benthic Fauna. Microbial Ecology 34: 131–143.

    Article  PubMed  Google Scholar 

  • Guys, C. M. & J. O’Keeffe, 1997. Simple words and fuzzy zones: early directions for temporary river research in South Africa. Environmental Management 21: 517–531.

    Article  Google Scholar 

  • Hall, R. O. Jr. & J. L. Meyer, 1998. The trophic significance of bacteria in a detritus-based stream food web. Ecology 79: 1995–2012.

    Article  Google Scholar 

  • Haynes, K., T. A. Hofmann, C. J. Smith, A. S. Ball, G. J. C. Underwood & A. Mark, 2007. Diatom-derived carbohydrates as factors affecting bacterial community composition in estuarine sediments. Applied and Environmental Microbiology 73: 6112–6124.

    Article  CAS  PubMed  Google Scholar 

  • Hill, B. H. & T. J. Gardner, 1987. Benthic metabolism in a perennial and an intermittent Texas prairie stream. Southwestern Naturalist 32: 305–311.

    Article  Google Scholar 

  • Hill, B. H., R. K. Hall, P. Husby, A. T. Herlihy & M. Dunne, 2000. Interregional comparison of sediment microbial respiration in stream. Freshwater Biology 44: 213–222.

    Article  Google Scholar 

  • Holms, R. M., S. G. Fisher, N. B. Grimm & B. J. Harper, 1998. The impact of flash floods on microbial distribution and biogeochemistry in the parafluvial zone of a desert stream. Freshwater Biology 40: 641–654.

    Article  Google Scholar 

  • Hoppe, H. G., 2003. Phosphatase activity in the sea. Hydrobiologia 493: 187–200.

    Article  CAS  Google Scholar 

  • Hubas, C., D. Davoult, T. Cariou & L. F. Artigas, 2006. Factors controlling benthic metabolism during low tide along a granulometric gradient in an intertidal bay (Roscoff Aber Bay, France). Marine Ecology Progress Series 316: 53–68.

    Article  CAS  Google Scholar 

  • IPCC, 2007. Summary for polymakers. In Salomon, S., M. Qin, M. Manning, Z. C. Chen, M. Marquis, K. B. Avergt, M. Tignor & H. L. Miller (eds), Climate Change 2007: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. Cambridge University Press, Cambridge, UK: 18 pp.

    Google Scholar 

  • Jones, J. B. Jr., S. G. Fisher & N. B. Grimm, 1995. Vertical hydrologic exchange and ecosystem metabolism in a Sonoran Desert stream. Ecology 76: 942–952.

    Article  Google Scholar 

  • Kirkby, M. J., 2005. Organisation and process. In Anderson, M. G. (ed.), Encyclopedia of Hydrological Sciences, Vol. 1. John Wiley, Chichester, UK: 41–58.

    Google Scholar 

  • Kirschner, A. K. T. & B. Velimirov, 1999. Benthic bacterial secondary production measured via simultaneous 3H-thymidine and 14Cleucine incorporation, and its implication for the carbon cycle of a shallow macrophyte dominated backwater system. Limnology and Oceanography 44: 1871–1881.

    Article  CAS  Google Scholar 

  • Koch, A. L., 1994. Growth measurement. In Gerhardt, P., R. G. E. Murray, W. A. Wood & N. R. Krieg (eds), Methods for General and Molecular Bacteriology. American Society for Microbiology, Washington, DC: 248–277.

    Google Scholar 

  • Logue, J. B., C. T. Robinson, C. Meier & J. R. Van der Meer, 2004. Relationship between sediment organic matter, bacterial composition, and the ecosystem metabolism of alpine streams. Limnology and Oceanography 49: 2001–2010.

    Article  Google Scholar 

  • Logue, J. B., H. Bürgmann & C. T. Robinson, 2008. Progress in the ecological genetics and biodiversity of freshwater bacteria. Bioscience 58: 103–113.

    Article  Google Scholar 

  • Lo Porto A., A. Puddu, L. Diliberto, G. Cané, A.M. De Girolamo, A. Zoppini, S. Fazi, S. Amalfitano, A. Barra Caracciolo & P. Grenni, 2006. SW Sardinia, Italy – Flumendosa Mulargia. In J. Froebrich & M. Bauer (eds), Critical Issue in the Water Quality Dynamics of Temporary Waters. Evaluation and Recommendations from the TempQsim Project. University of Hannover, Hannover, Germany: 31–36.

    Google Scholar 

  • Loy, A., M. Horn & M. Wagner, 2003. ProbeBase: an online resource for rRNA-targeted oligonucleotide probes. Nucleic Acids Research 31: 514–516.

    Article  CAS  PubMed  Google Scholar 

  • Marxsen, J., 2006. Bacterial production in the carbon flow of a central European stream, the Breitenbach. Freshwater Biology 51: 1838–1861.

    Article  CAS  Google Scholar 

  • Marxsen, J. & D. M. Fiebig, 1993. Use of perfused cores for evaluating extracellular enzyme activity in stream-bed sediments. FEMS Microbial Ecology 11: 1–11.

    Article  Google Scholar 

  • Marxsen, J., A. Zoppini & S. Wilczek, 2010. Microbial communities in streambed sediments recovering from desiccation. FEMS Microbiology Ecology 71: 374–386.

    Article  CAS  PubMed  Google Scholar 

  • Milly, P. C. D., K. A. Dunne & A. V. Vecchia, 2005. Global pattern of trends in streamflow and water availability in a changing climate. Nature Letters 438: 17.

    Google Scholar 

  • Mulholland, P. J., 2003. Large-scale patterns in dissolved organic carbon concentration, flux and sources. In Findlay, S. E. & R. L. Sinsabaugh (eds), Aquatic Ecosystems, Interactivity of Dissolved Organic Matter. Academic Press, Elsevier, San Diego: 139–159.

    Google Scholar 

  • Mulholland, P. J., C. S. Fellows, J. L. Tank, N. B. Grimm, J. R. Webster, S. K. Hamilton, E. Marti, L. Ashkenas, W. B. Bowden, W. K. Dodds, W. H. McDowell, M. J. Paul & B. J. Peterson, 2001. Inter-biome comparison of factors controlling stream metabolism. Freshwater Biology 46: 1503–1517.

    Article  CAS  Google Scholar 

  • Mulholland, P. J., J. N. Houser & K. O. Maloney, 2005. Stream diurnal dissolved oxygen profiles as indicators of in-stream metabolism and disturbance effects: Fort Benning as a case study. Ecological Indicators 5: 243–252.

    Article  CAS  Google Scholar 

  • Naegeli, M. W., U. Hartmann, E. I. Meyer & U. Uehlinger, 1995. POM dynamics and community respiration in the sediments of a floodprone prealpine river (Necker, Switzerland). Archiv für Hydrobiologie 133: 339–347.

    Google Scholar 

  • Pernthaler, J., F. O. Glöckner, W. Schönhuber & R. Amann, 2001. Fluorescence in situ hybridization (FISH) with rRNA-targeted oligonucleotide probes. Methods in Microbiology 30: 207–226.

    Article  CAS  Google Scholar 

  • Romani, A. M. & S. Sabater, 2001. Structure and activity of rock and sand biofilms in Mediterranean stream. Ecology 82: 3232–3245.

    Google Scholar 

  • Romani, A. M., A. Butturini, F. Sabater & S. Sabater, 1998. Heterotrophic metabolism in a forest stream sediment: surface versus subsurface zones. Aquatic Microbial Ecology 16: 143–151.

    Article  Google Scholar 

  • Romani, A. M., E. Vasquez & A. Butturini, 2006. Microbial availability and size fractionation of dissolved organic carbon after drought in an intermittent stream: biogeochemical link across the stream-riparian interface. Microbial Ecology 52: 501–512.

    Article  CAS  PubMed  Google Scholar 

  • Sala, M., M. Karner, L. Arin & C. Marrasé, 2001. Measurement of ectoenzyme activities as an indication of inorganic nutrient imbalance in microbial communities. Aquatic Microbial Ecology 23: 301–311.

    Article  Google Scholar 

  • Smith, D. C. & F. Azam, 1992. A simple, economical method for measuring bacterial protein synthesis rates in seawater using 3H-leucine. Marine Microbial Food Webs 6: 107–114.

    Google Scholar 

  • Taylor, G. T., J. W. Ying Yu & M. I. Scranton, 2003. Ectohydrolase activity in surface waters of the Hudson River and western Long Island Sound estuaries. Marine Ecology Progress Series 263: 1–15.

    Article  CAS  Google Scholar 

  • Törnblom, E., 1996. Bacterial production and total community metabolism in sediments of a eutrophic lake. Archiv für Hydrobiologie, Special Issues: Advances in Limnology. 48: 207–216.

    Google Scholar 

  • Tzoraky, O. & N. P. Nikolaidis, 2007. A generalized framework for modelling the hydrologic and biogeochemical response of a Mediterranean temporary river basin. Journal of Hydrology 346: 112–121.

    Article  Google Scholar 

  • Tzoraky, O., N. P. Nikolaidis, Y. Amaxidis & N. T. H. Skoulikidis, 2007. In-stream biogeochemical processes of a temporary river. Environmental Science and Technology 41: 1225–1231.

    Article  Google Scholar 

  • Uehlinger, U. & J. T. Brock, 1991. The assessment of river periphyton metabolism: a method and some problems. In Whitton, B. A., E. Rott & G. Friedrich (eds), Use of Algae for Monitoring Rivers. Universität Innsbruck. Institute für Botanik, Innsbruck, Austria: 175–181.

    Google Scholar 

  • Uehlinger, U. & M. W. Naegeli, 1998. Ecosystem metabolism, disturbance, and stability in a prealpine gravel bed river. Journal of the North American Benthological Society 17: 165–178.

    Article  Google Scholar 

  • Uehlinger, U., M. W. Naegeli & S. G. Fisher, 2002. A heterotrophic desert stream? The role of sediment stability. Western North American Naturalist 62: 466–473.

    Google Scholar 

  • Valett, H. M., S. G. Fisher, N. B. Grimm & P. Camill, 1994. Vertical hydrologic exchange and ecological stability of a desert stream ecosystem. Ecology 75: 548–560.

    Article  Google Scholar 

  • WFD/EUWI, 2006. Mediterranean Joint Process WFD/EUWI, Water Scarcity Drafting Group, Tool Box (Best practices) on water scarcity, Draft Version Number 9, to be modified, 13th February 2006.

    Google Scholar 

  • Wilczek, S., H. Fischer & M. T. Pusch, 2005. Regulation and seasonal dynamics of extracellular enzyme activities in the sediments of a large lowland river. Microbial Ecology 50: 253–267.

    Article  CAS  PubMed  Google Scholar 

  • Wilmes, P. & P. L. Bond, 2009. Microbial community proteomics: elucidating the catalysts and metabolic mechanisms that drive the Earth’s biogeochemical cycles. Current Opinion in Microbiology 12: 1–8.

    Article  Google Scholar 

  • Wobus, A., C. Bleul, S. Maassen, C. Scheerer, M. Schuppler, E. Jacobs & I. Röske, 2003. Microbial diversity and functional characterization of sediments from reservoirs of different trophic state. FEMS Microbiology and Ecology 46: 331–347.

    Article  CAS  Google Scholar 

  • Zoppini, A. & J. Marxsen, 2010. Importance of Extracellular Enzymes for Biogeochemical Processes in Temporary River Sediments during Fluctuating Dry-Wet Conditions. In Shukla, G. & A. Varma (eds), Soil Enzymology, Soil Biology Series. Springer, Berlin: in press

    Google Scholar 

  • Zoppini, A., A. Puddu, S. Fazi, M. Rosati & P. Sist, 2005. Extracellular enzyme activity and dynamics of bacterial community in mucilaginous aggregates of the northern Adriatic Sea. Science of the Total Environment 353: 270–286.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Annamaria Zoppini .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2010 Springer Science+Business Media B.V.

About this chapter

Cite this chapter

Zoppini, A., Amalfitano, S., Fazi, S., Puddu, A. (2010). Dynamics of a benthic microbial community in a riverine environment subject to hydrological fluctuations (Mulargia River, Italy). In: Stevenson, R.J., Sabater, S. (eds) Global Change and River Ecosystems—Implications for Structure, Function and Ecosystem Services. Developments in Hydrobiology 215, vol 215. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-0608-8_4

Download citation

Publish with us

Policies and ethics