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Shifts in Microbial Community Composition Following Surface Application of Dredged River Sediments

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Abstract

Sediment input to the Illinois River has drastically decreased river depth and reduced habitats for aquatic organisms. Dredging is being used to remove sediment from the Illinois River, and the dredged sediment is being applied to the surface of a brownfield site in Chicago with the goal of revegetating the site. In order to determine the effects of this drastic habitat change on sediment microbial communities, we examined sediment physical, chemical, and microbial characteristics at the time of sediment application to the soil surface as well as 1 and 2 years after application. Microbial community biomass was determined by measurement of lipid phosphate. Microbial community composition was assessed using phospholipid fatty acid (PLFA) analysis, terminal restriction fragment length polymorphism (T-RFLP) analysis of 16S rRNA genes, and clone library sequencing of 16S rRNA genes. Results indicated that the moisture content, organic carbon, and total nitrogen content of the sediment all decreased over time. Total microbial biomass did not change over the course of the study, but there were significant changes in the composition of the microbial communities. PLFA analysis revealed relative increases in fungi, actinomycetes, and Gram positive bacteria. T-RFLP analysis indicated a significant shift in bacterial community composition within 1 year of application, and clone library analysis revealed relative increases in Proteobacteria, Gemmatimonadetes, and Bacteriodetes and relative decreases in Acidobacteria, Spirochaetes, and Planctomycetes. These results provide insight into microbial community shifts following land application of dredged sediment.

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References

  1. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ (1990) Basic local alignment search tool. J Mol Biol 215:403–410

    PubMed  CAS  Google Scholar 

  2. Bear FE (1955) Chemistry of the soil. Reinhold, New York

    Google Scholar 

  3. Bhowmik NG, Demissie M, Marlin JC, Mick J (2000) Integrated management of the Illinois River with an emphasis on the ecosystem. In: Marino MA, Simonovic SP (eds) Integrated Water Resources Management (Proceedings of a Symposium). International Association for Hydrologic Sciences, Paris, pp 365–370, International Association for Hydrologic Sciences Publication no. 272

    Google Scholar 

  4. Borneman J, Skroch PW, O’Sullivan KM, Palus JA, Rumjanek NG, Jansen JL, Nienhuis J, Triplett EW (1996) Molecular microbial diversity of an agricultural soil in Wisconsin. Appl Environ Microbiol 62:1935–1943

    PubMed  CAS  Google Scholar 

  5. Bossio DA, Scow KM (1998) Impacts of carbon and flooding on soil microbial communities: phospholipid fatty acid profiles and substrate utilization patterns. Microb Ecol 35:265–278

    Article  PubMed  CAS  Google Scholar 

  6. Bray JR, Curtis JT (1957) An ordination of the upland forest communities of Southern Wisconsin. Ecol Monogr 27:325–349

    Article  Google Scholar 

  7. Canet R, Chaves C, Pomares F, Albiach R (2003) Agricultural use of sediments from the Albufera Lake (Eastern Spain). Agric Ecosyst Environ 95:29–36

    Article  Google Scholar 

  8. Clarke KR, Warwick RM (2001) A further biodiversity index applicable to species lists: variation in taxonomic distinctness. Mar Ecol Prog Ser 216:265–278

    Article  Google Scholar 

  9. Darmody RG, Marlin JC, Talbot J, Stohr C, Green R, Brewer EF (2004) Dredged Illinois River sediments: plant growth and metal uptake in Illinois River sediments. J Environ Qual 33:458–464

    Article  PubMed  CAS  Google Scholar 

  10. Drenovsky RE, Vo D, Graham KJ, Scow KM (2004) Soil water content and organic carbon availability are major determinants of soil microbial community composition. Microb Ecol 48:424–430

    Article  PubMed  CAS  Google Scholar 

  11. Environmental Protection Agency (1996) Test methods for evaluating solid waste: physical–chemical methods. EPA, Washington, D.C., EPA SW-846, Chapter 3

    Google Scholar 

  12. Environmental Protection Agency (1993) Methods for the determination of inorganic substances in environmental samples. EPA, Washington, D.C., EPA/600/R-93/100

    Google Scholar 

  13. Fierer N, Bradford MA, Jackson RB (2007) Toward an ecological classification of soil bacteria. Ecology 88:1354–1364

    Article  PubMed  Google Scholar 

  14. Frostegard A, Tunlid A, Baath E (1991) Microbial biomass measured as total lipid phosphate in soils of different organic content. J Microbiol Meth 14:151–163

    Article  Google Scholar 

  15. Gardner WH (1986) Water content. In: Klute A (ed) Methods of soil analysis, Part I. Soil Science Society of America, Madison, pp 493–544

    Google Scholar 

  16. Howarth RW, Fruci JR, Sherman D (1991) Inputs of sediment and carbon to an estuarine ecosystem: influence of land use. Ecol Appl 1:27–39

    Article  Google Scholar 

  17. Iverson LR (1988) Land-use changes in Illinois, USA: the influence of landscape attributes on current and historic land use. Landsc Ecol 2:45–61

    Article  Google Scholar 

  18. Janus LR, Angeloni NL, McCormack J, Rier ST, Tuchman NC, Kelly JJ (2005) Elevated atmospheric CO2 alters soil microbial communities associated with trembling aspen (Populus tremuloides) roots. Microb Ecol 50:102–109

    Article  PubMed  Google Scholar 

  19. Jaatinen K, Fritze H, Laine J, Laiho R (2007) Effects of short- and long-term water-level drawdown on the populations and activity of aerobic decomposers in a boreal peatland. Glob Change Biol 13:491–510

    Article  Google Scholar 

  20. Kane MD, Poulsen LK, Stahl DA (1993) Monitoring the enrichment and isolation of sulfate-reducing bacteria by using oligonucleotide hybridization probes designed from environmentally derived 16S ribosomal RNA sequences. Appl Environ Microbiol 59:682–686

    PubMed  CAS  Google Scholar 

  21. Kelly JJ, Tate RL (1998) Effects of heavy metal contamination and remediation on soil microbial communities in the vicinity of a zinc smelter. J Environ Qual 27:609–617

    CAS  Google Scholar 

  22. Kelly JJ, Haggblom M, Tate RL (1999) Changes in soil microbial communities over time resulting from one time application of zinc: a laboratory microcosm study. Soil Biol Biochem 31:1455–1465

    Article  CAS  Google Scholar 

  23. Lembke WD, Mitchell JK, Fehrenbacher JB, Barcelona MJ (1983) Dewatering dredged sediment for agriculture. T Am Soc Ag Eng 26:808–813

    Google Scholar 

  24. Lembke WD, Mitchell JK, Fehrenbacher JB, Barcelona MJ (1983) Illinois Water Resources Center Research, Urbana Illinois, Water Resources Center Research Report No 175

  25. Liu W, Marsh TL, Cheng H, Forney LJ (1997) Characterization of microbial diversity by determining terminal restriction fragment length polymorphisms of genes encoding 16S rRNA. Appl Environ Microbiol 63:4516–4522

    PubMed  CAS  Google Scholar 

  26. Luyssaert S, Mertens J, Vervaeke P, de Vos B, Lust N (2001) Preliminary results of afforestation of brackish sludge mounds. Ecol Eng 16:567–572

    Article  Google Scholar 

  27. Machesky ML, Slowikowski JA, Cahill RA, Bogner WC, Marlin JC, Holm TR, Darmody RG (2005) Sediment quality and quantity issues related to the restoration of backwater lakes along the Illinois River waterway. Aquat Ecosys Health Manag 8:33–40

    Article  CAS  Google Scholar 

  28. Marilley L, Aragno M (1999) Phylogenetic diversity of bacterial communities differing in degree of proximity of Lolium perenne and Trifolium repens roots. Appl Soil Ecol 13:127–136

    Article  Google Scholar 

  29. McCarthy AJ (1987) Lignocellulose degrading actinomycetes. FEMS Microbiol Lett 46:145–163

    Article  CAS  Google Scholar 

  30. MIDI (1995) Sherlock microbial identification system operating manual: version 5. MIDI, Newark

    Google Scholar 

  31. Myrold DD (1994) Frankia and the actinorhizal symbiosis. In: Weaver RW, Angle JS, Bottomley PS (eds) Methods of soil analysis. Soil Science Society of America, Madison, pp 329–350

    Google Scholar 

  32. Parkinson D (1994) Filamentous fungi. In: Weaver RW, Angle JS, Bottomley PS (eds) Methods of soil analysis. Soil Science Society of America, Madison, pp 329–350

    Google Scholar 

  33. Peijnenburg W, de Groot A, Jager T, Posthuma L (2005) Short-term ecological risks of depositing contaminated sediment on arable soil. Ecotoxicol Environ Saf 60:1–14

    Article  PubMed  CAS  Google Scholar 

  34. Pennanen T (2001) Microbial communities in boreal coniferous forest humus exposed to heavy metals and changes in soil pH—a summary of the use of phospholipid fatty acids, Biolog and H-3-thymidine incorporation methods in field studies. Geoderma 100:91–126

    Article  CAS  Google Scholar 

  35. Peterson SA (1982) Lake restoration by sediment removal. Wat Res Bull 18:423–435

    CAS  Google Scholar 

  36. Rees GN, Watson GO, Baldwin DS, Mitchell AM (2006) Variability in sediment microbial communities in a semipermanent stream: impact of drought. J North Am Benthol Soc 25:370–378

    Article  Google Scholar 

  37. Stephen JR, McCaig AE, Smith Z, Prosser JI, Embley TM (1996) Molecular diversity of soil and marine 16S rRNA gene sequences related to beta-subgroup ammonia-oxidizing bacteria. Appl Environ Microbiol 62:4147–54

    PubMed  CAS  Google Scholar 

  38. Sylvia DM (1994) Vesicular-arbuscular mycorrhizal fungi. In: Weaver RW, Angle JS, Bottomley PS (eds) Methods of soil analysis. Soil Science Society of America, Madison, pp 351–378

    Google Scholar 

  39. Thomas GW (1996) Soil ph and soil acidity. In: Sparks DL (ed) Methods of soil analysis. Soil Science Society of America, Madison, pp 475–490

    Google Scholar 

  40. Walling DE (1999) Linking land use, erosion and sediment yields in river basins. Hydrobiologia 410:223–240

    Article  Google Scholar 

  41. Waters TF (1995) Sediment in streams: sources, biological effects, and control. American Fisheries Society Monograph, Bethesda, American Fisheries Society Monograph no. 7

    Google Scholar 

  42. Wellington EMH, Toth IK (1994) Actinomycetes. In: Weaver RW, Angle JS, Bottomley PS (eds) Methods of soil analysis. Soil Science Society of America, Madison, pp 269–290

    Google Scholar 

  43. White DC, Davis WM, Nickels JS, King JD, Bobbie RJ (1979) Determination of the sedimentary microbial biomass by extractable lipid phosphate. Oecologia 40:51–62

    Article  Google Scholar 

  44. Zak DR, Ringelberg DB, Pregitzer KS, Randlett DL, White DC, Curtis PS (1996) Soil microbial communities beneath Populus grandidentata grown under elevated atmospheric CO2. Ecol Appl 6:257–262

    Article  Google Scholar 

  45. Zar JH (1999) Biostatistical analysis. Prentice Hall, Upper Saddle River

    Google Scholar 

  46. Zarda B, Hahn D, Chatzinotas A, Schönhuber W, Neef A, Amann RI, Zeyer J (1997) Analysis of bacterial community structure in bulk soil by in situ hybridization. Arch Microbiol 168:185–192

    Article  CAS  Google Scholar 

  47. Zhang H, Sekiguchi Y, Hanada S, Hugenholtz P, Kim H, Kamagata Y, Nakamura K (2003) Gemmatimonas aurantiaca gen. nov., sp. nov., a gram-negative, aerobic, polyphosphate-accumulating micro-organism, the first cultured representative of the new bacterial phylum Gemmatimonadetes phyl. nov. Int J Syst Evol Microbiol 53:1155–63

    Article  PubMed  CAS  Google Scholar 

  48. Zwart G, Crump BC, Kamst-van Agterveld MP, Hagen F, Han SK (2002) Typical freshwater bacteria: an analysis of available 16S rRNA gene sequences from plankton of lakes and rivers. Aquat Micr Ecol 28:141–155

    Article  Google Scholar 

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Acknowledgements

This work was supported by a grant to JJK from the Illinois Waste Management and Research Center of the Illinois Department of Natural Resources. DB was supported by funding from the Center for Urban Environmental Research and Policy at Loyola University Chicago and the Loyola University Mulcahy Scholar’s Program. The authors thank John C. Marlin from the Waste Management and Research Center for establishing the treatment plots and for providing access to the site. The authors also thank Max Haggblom for assistance with PLFA analysis and Martin Berg for assistance with MDS analyses.

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Correspondence to John J. Kelly.

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Baniulyte, D., Favila, E. & Kelly, J.J. Shifts in Microbial Community Composition Following Surface Application of Dredged River Sediments. Microb Ecol 57, 160–169 (2009). https://doi.org/10.1007/s00248-008-9410-y

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  • DOI: https://doi.org/10.1007/s00248-008-9410-y

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