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Distinct changes in riparian sediment microbial communities with depth and time since dam removal


Abstract

Microbes drive biogeochemical changes in ecosystems, including carbon (C) and nitrogen (N) cycling. Dam construction has altered riparian ecosystems worldwide, yet we know little about microbial community composition in riparian sediments and how it changes following dam removal and sediment/soil drainage. Here, we evaluate how riparian microbial communities change with increasing depth in the sediment profile for existing dams and over time following dam removal/breach and assess how various physico-chemical sediment properties influence microbial community composition. We studied microbial community structure for 12 riparian sites over a chronosequence of 0-234 years since dam breach. Sediment was collected every 0.3 m to a depth of 4 m. Aerobic taxa involved with N cycling (e.g., Nitrospirota) were dominant in surficial sediments, and increased in deeper sediments as time since dam breach increased. Anaerobic taxa implicated in C cycling (e.g., Bathyarchaeia, Anaerolineaceae) and iron reduction (e.g., Sva0485) were dominant in deeper, anoxic sediments, but declined the fastest post dam breach. These microbial trends provide insights into how riparian biogeochemical functions are impacted by dam inundation and the recovery and restoration of these ecosystems following dam removals.

Data availability

The datasets generated and/or analyzed during the current study are available in the GenBank repository, [accession number PRJNA1346466].

References

  1. Fierer, N. Embracing the unknown: Disentangling the complexities of the soil microbiome. Nat. Rev. Microbiol. 15, 579–590 (2017).

  2. Steger, K., Kim, A. T., Ganzert, L., Grossart, H. & Smart, D. R. Floodplain soil and its bacterial composition are strongly affected by depth. FEMS Microbiol. Ecol. 95 (3), fiz014 (2019).

  3. Naylor, D., Mcclure, R. & Jansson, J. Trends in microbial community composition and function by soil depth. Microorganisms 10 (3), 540 (2022).

  4. Krause, S. et al. Ecohydrological interfaces as hot spots of ecosystem processes. Water Resour. Res. 53, 6359–6376 (2017).

  5. Vidon, P. et al. Hot spots and hot moments in riparian zones: potential for improved water quality management. J. Am. Water Resour. Assoc. 46, 278–298 (2010).

    Google Scholar 

  6. Chen, J. et al. Bacterial communities in riparian sediments: A large-scale longitudinal distribution pattern and response to dam construction. Front. Microbiol. 9, 999 (2018).

  7. Inamdar, S. et al. Ghosts of landuse past: Legacy effects of milldams for riparian nitrogen (N) processing and water quality functions. Environ. Res. Lett. 16, 035016 (2021).

  8. Kan, J., Peck, E. K., Zgleszewski, L., Peipoch, M. & Inamdar, S. Mill dams impact Microbiome structure and depth distribution in riparian sediments. Front. Microbiol. 14, 1161043 (2023).

    Google Scholar 

  9. Graham, E. B., Stegen, J. C., Huang, M., Chen, X. & Scheibe, T. D. Subsurface biogeochemistry is a missing link between ecology and hydrology in dam-impacted river corridors. Sci. Total Environ. 657, 435–445 (2019).

    Google Scholar 

  10. Zhou, X., Lennon, J. T., Lu, X. & Ruan, A. Anthropogenic activities mediate stratification and stability of microbial communities in freshwater sediments. Microbiome 11, 191 (2023).

  11. Anderson, E. P. et al. Fragmentation of Andes-to-Amazon connectivity by hydropower dams. Sci. Adv. 4, eaao1642 (2018).

    Google Scholar 

  12. Foley, M. M. et al. Dam removal: listening in. Water Resour. Res. 53, 5229–5246 (2017).

    Google Scholar 

  13. Eilers, K. G., Debenport, S., Anderson, S. & Fierer, N. Digging deeper to find unique microbial communities: The strong effect of depth on the structure of bacterial and archaeal communities in soil. Soil Biol. Biochem. 50, 58–65 (2012).

  14. Wu, X. et al. Distinct depth-discrete profiles of microbial communities and geochemical insights in the subsurface critical zone. Appl. Environ. Microbiol. 89 (6), e0050023 (2023).

  15. Brewer, T. E. et al. Ecological and genomic attributes of novel bacterial taxa that thrive in subsurface soil horizons. mBio 10 (5), e01318-19 (2019).

  16. James, L. A. Legacy sediment: definitions and processes of episodically produced anthropogenic sediment. Anthropocene 2, 16–26 (2013).

    Google Scholar 

  17. Livers, B. & Snyder, N. P. Legacy sediment: A conceptual model and perspective on the role of dams. Earth Surf. Processes Landf. 50, e70044 (2025).

  18. Merritts, D. et al. Anthropocene streams and base-level controls from historic dams in the unglaciated mid-Atlantic region, USA. Philosophical Transactions: Math. Phys. Eng. Sci. 369, 976–1009 (2011).

    Google Scholar 

  19. Walter, R. C. & Merritts, D. J. Natural streams and the legacy of Water-Powered mills. Science 319, 299–304 (2008).

    Google Scholar 

  20. Peck, E. K., Inamdar, S. P., Peipoch, M. & Gold, A. J. Influence of relict milldams on riparian sediment biogeochemistry. J. Soils Sediments. 23, 2584–2599 (2023).

    Google Scholar 

  21. Peck, E. K. et al. Back from the past? Assessment of nitrogen removal ability of buried historic wetland soils before and after a 1-year incubation on a restored floodplain. Restor. Ecol. 32 (3), e14070 (2023).

  22. Weitzman, J. N. & Kaye, J. P. Nitrate retention capacity of milldam-impacted legacy sediments and relict A horizon soils. SOIL 3, 95–112 (2017).

    Google Scholar 

  23. Inamdar, S. P. et al. Saturated, suffocated, and salty: Human legacies produce hot spots of nitrogen in riparian zones. JGR Biogeosciences 127, e2022JG007138 (2022).

  24. Sherman, M. et al. Backed-Up, Saturated, and Stagnant: Effect of Milldams on Upstream Riparian Groundwater Hydrologic and Mixing Regimes. Water Resour. Res. 58, n/a (2022).

  25. Merritts, D. et al. The rise and fall of Mid-Atlantic streams: millpond sedimentation, milldam breaching, channel incision, and stream bank erosion. Geol. Soc. Am. Reviews Eng. Geol. XXI, 183–203 (2013).

    Google Scholar 

  26. Lewis, E. et al. Draining the landscape: How do nitrogen concentrations in riparian groundwater and stream water change following milldam removal? JGR Biogeosciences 126 (8), e2021JG006444 (2021).

  27. Moore, E. et al. Evolution of riparian terrace sediments following dam removal and soil drainage: A chronosequence study. 2024 AGU Fall Meeting, Washington DC. Abstract # EP14B-04 (2024). Online: https://agu.confex.com/agu/agu24/meetingapp.cgi/Paper/1659238 (accessed January 25, 2026).

  28. Sena, M. G. et al. Seasonal variation and key controls of groundwater ammonium concentrations in Hypoxic/Anoxic riparian sediments. JGR Biogeosciences 130, e2023JG007900 (2025).

  29. Peck, E. K. et al. Nitrogen sinks or sources? Denitrification and nitrogen removal potential in riparian legacy sediment terraces affected by milldams. JGR Biogeosciences 127 (10), e2022JG007004 (2022).

  30. Rahman, M. M. et al. Dissimilatory nitrate reduction to ammonium (DNRA) can undermine nitrogen removal effectiveness of persistently reducing riparian sediments. ACS EST. Water. 4, 3873 (2024).

    Google Scholar 

  31. Merritts, D. & Rahnis, M. Pleistocene periglacial processes and Landforms, Mid-Atlantic Region, Eastern united States. Annu. Rev. Earth Planet. Sci. 50, 541–592 (2022).

    Google Scholar 

  32. Cashman, M. J. et al. Hidden legacies: investigating buried pre-colonial stream corridors in the Mid-Atlantic coastal Plain, Maryland, USA. Ecol. Eng. 221, 107771 (2025).

  33. Elliott, S. J., Wilf, P., Walter, R. C. & Merritts, D. J. Subfossil leaves reveal a new upland hardwood component of the pre-European Piedmont landscape, Lancaster County, Pennsylvania. PLoS One. 8, e79317 (2013).

    Google Scholar 

  34. Mattern, K. et al. Stream restoration for legacy sediments at Gramies Run, maryland: early lessons from Implementation, water quality Monitoring, and soil health. Water (Basel). 12, 2164 (2020).

    Google Scholar 

  35. Sienkiewicz, N. et al. Bacterial communities and nitrogen transformation genes in streambank legacy sediments and implications for biogeochemical processing. Biogeochemistry 148, 271–290 (2020).

    Google Scholar 

  36. Lutgen, A. et al. Nutrients and heavy metals in legacy sediments: Concentrations, comparisons with upland Soils, and implications for water quality. J. Am. Water Resour. Association. 56, 669–691 (2020).

    Google Scholar 

  37. Blazewicz, S. J., Barnard, R. L., Daly, R. A. & Firestone, M. K. Evaluating rRNA as an indicator of microbial activity in environmental communities: limitations and uses. ISME J. 7, 3061–2068 (2013).

    Google Scholar 

  38. Lazar, C. S. et al. Genomic evidence for distinct carbon substrate preferences and ecological niches of bathyarchaeota in estuarine sediments. Environ. Microbiol. 18 (4), 1200–1211 (2016).

  39. Freches, A. & Fradinho, J. C. The biotechnological potential of the Chloroflexota phylum. Appl. Environ. Microbiol. 90, e01756-23 (2024).

  40. Wen, W. et al. Dissimilatory nitrate reduction to ammonium driven by different electron donors: Mechanisms, recent advances, and future perspectives. Chem. Eng. J. 507, 160625 (2025).

  41. Liu, H. et al. Biogeochemical cycles of iron: Processes, mechanisms, and environmental implications. Sci. Total Environ. 951, 175722 (2024).

  42. Tan, S. et al. Insights into ecological role of a new deltaproteobacterial order candidatus acidulodesulfobacterales by metagenomics and metatranscriptomics. The ISME Journal 13, 2044–2057 (2019).

  43. Yu, T. et al. Widespread Bathyarchaeia encode a novel methyltransferase utilizing lignin-derived aromatics. mLife 2, 272–282 (2023).

  44. Zhao, N. et al. Dissimilatory iron-reducing microorganisms: the phylogeny, physiology, applications and outlook. Crit. Rev. Environ. Sci. Technol. 55 (2), 73–98 (2024).

  45. Argiroff, W. A., Zak, D. R., Lanser, C. M. & Wiley, M. J. Microbial community functional potential and composition are shaped by hydrologic connectivity in riverine floodplain soils. Microb. Ecol. 73, 630–644 (2017).

  46. Janssen, P. H. Identifying the dominant soil bacterial taxa in libraries of 16S rRNA and 16S rRNA genes. Appl. Environ. Microbiol. 72, 1719–1728 (2006).

  47. Hilderbrand, R. H., Bambakidis, T. & Crump, B. C. The roles of microbes in stream restorations. Microb. Ecol. 85, 853–861 (2023).

  48. Mafa-Attoye, T. G. et al. Bacterial community structure and resilience are partially restored after 30 years of rehabilitation of an agricultural riparian system. Agric. Ecosyst. Environ. 393 (1), 109813 (2025).

  49. Singh Rawat, V., Kaur, J., Bhagwat, S. & Arora Pandit, M. & Dogra Rawat, C. Deploying microbes as drivers and indicators in ecological restoration. Restor. Ecol. 31 (1), e13688 (2023).

  50. Frostegård, Å., Tunlid, A. & Bååth, E. Use and misuse of PLFA measurements in soils. Soil Biol. Biochem. 43, 1621–1625 (2011).

    Google Scholar 

  51. Mehra, O. P. & Jackson, M. L. Iron oxide removal from soils and clays by dithionite- citrate system buffered with sodium dicarbonate. Clay Mineraology. 7, 317–327 (1960).

    Google Scholar 

  52. Lair, G. J. et al. Dating of soil layers in young floodplain using iron oxide crystallinity. Quat. Geochronol. 4, 260–266 (2009).

    Google Scholar 

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Acknowledgements

This study was funded by the US Department of Agriculture NIFA grant award # 2023-67019-39835. We would like to thank Jessie Thomas-Blate from American Rivers and the many landowners who provided us access to the milldam sites for sampling. Soil/sediment analysis was provided by Regen Ag Lab and the University of Delaware Soils lab. We also thank Drs. Dorothy Merritts and Robert Walter for their guidance on the study.

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Eric R. Moore (EM) and Shreeram Inamdar (SI) wrote the article. EM, Md. Moklesur Rahman (MR), Matthew Sena (MS), Joseph G. Galella (JG), Bisesh Joshi (BJ), and Alexis Yaculak (AY) collected the data. Marc Peipoch (MP) conducted denitrification enzyme assays and Jinjun Kan (JK) performed high throughput sequencing steps. EM did the data analysis and created the tables and figures. All authors reviewed the manuscript and suggested edits.

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Eric R. Moore or Shreeram Inamdar.

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Moore, E.R., Rahman, M.M., Galella, J.G. et al. Distinct changes in riparian sediment microbial communities with depth and time since dam removal.
Sci Rep (2026). https://doi.org/10.1038/s41598-026-37708-3

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  • DOI: https://doi.org/10.1038/s41598-026-37708-3

Keywords

  • Soil microbiome
  • Soil drainage
  • Dam removal
  • Nitrogen cycling
  • Anaerobic sediments
  • Iron reduction
  • Buried hydric soils


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