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Mill dams impact microbiome structure and depth distribution in riparian sediments

INTRODUCTION: Damming has substantially fragmented and altered riverine ecosystems worldwide. Dams slow down streamflows, raise stream and groundwater levels, create anoxic or hypoxic hyporheic and riparian environments and result in deposition of fine sediments above dams. These sediments represent...

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Autores principales: Kan, Jinjun, Peck, Erin K., Zgleszewski, Laura, Peipoch, Marc, Inamdar, Shreeram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339028/
https://www.ncbi.nlm.nih.gov/pubmed/37455732
http://dx.doi.org/10.3389/fmicb.2023.1161043
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author Kan, Jinjun
Peck, Erin K.
Zgleszewski, Laura
Peipoch, Marc
Inamdar, Shreeram
author_facet Kan, Jinjun
Peck, Erin K.
Zgleszewski, Laura
Peipoch, Marc
Inamdar, Shreeram
author_sort Kan, Jinjun
collection PubMed
description INTRODUCTION: Damming has substantially fragmented and altered riverine ecosystems worldwide. Dams slow down streamflows, raise stream and groundwater levels, create anoxic or hypoxic hyporheic and riparian environments and result in deposition of fine sediments above dams. These sediments represent a good opportunity to study human legacies altering soil environments, for which we lack knowledge on microbial structure, depth distribution, and ecological function. METHODS: Here, we compared high throughput sequencing of bacterial/ archaeal and fungal community structure (diversity and composition) and functional genes (i.e., nitrification and denitrification) at different depths (ranging from 0 to 4 m) in riparian sediments above breached and existing milldams in the Mid-Atlantic United States. RESULTS: We found significant location- and depth-dependent changes in microbial community structure. Proteobacteria, Bacteroidetes, Firmicutes, Actinobacteria, Chloroflexi, Acidobacteria, Planctomycetes, Thaumarchaeota, and Verrucomicrobia were the major prokaryotic components while Ascomycota, Basidiomycota, Chytridiomycota, Mortierellomycota, Mucoromycota, and Rozellomycota dominated fungal sequences retrieved from sediment samples. Ammonia oxidizing genes (amoA for AOA) were higher at the sediment surface but decreased sharply with depth. Besides top layers, denitrifying genes (nosZ) were also present at depth, indicating a higher denitrification potential in the deeper layers. However, these results contrasted with in situ denitrification enzyme assay (DEA) measurements, suggesting the presence of dormant microbes and/or other nitrogen processes in deep sediments that compete with denitrification. In addition to enhanced depth stratification, our results also highlighted that dam removal increased species richness, microbial diversity, and nitrification. DISCUSSION: Lateral and vertical spatial distributions of soil microbiomes (both prokaryotes and fungi) suggest that not only sediment stratification but also concurrent watershed conditions are important in explaining the depth profiles of microbial communities and functional genes in dammed rivers. The results also provide valuable information and guidance to stakeholders and restoration projects.
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spelling pubmed-103390282023-07-14 Mill dams impact microbiome structure and depth distribution in riparian sediments Kan, Jinjun Peck, Erin K. Zgleszewski, Laura Peipoch, Marc Inamdar, Shreeram Front Microbiol Microbiology INTRODUCTION: Damming has substantially fragmented and altered riverine ecosystems worldwide. Dams slow down streamflows, raise stream and groundwater levels, create anoxic or hypoxic hyporheic and riparian environments and result in deposition of fine sediments above dams. These sediments represent a good opportunity to study human legacies altering soil environments, for which we lack knowledge on microbial structure, depth distribution, and ecological function. METHODS: Here, we compared high throughput sequencing of bacterial/ archaeal and fungal community structure (diversity and composition) and functional genes (i.e., nitrification and denitrification) at different depths (ranging from 0 to 4 m) in riparian sediments above breached and existing milldams in the Mid-Atlantic United States. RESULTS: We found significant location- and depth-dependent changes in microbial community structure. Proteobacteria, Bacteroidetes, Firmicutes, Actinobacteria, Chloroflexi, Acidobacteria, Planctomycetes, Thaumarchaeota, and Verrucomicrobia were the major prokaryotic components while Ascomycota, Basidiomycota, Chytridiomycota, Mortierellomycota, Mucoromycota, and Rozellomycota dominated fungal sequences retrieved from sediment samples. Ammonia oxidizing genes (amoA for AOA) were higher at the sediment surface but decreased sharply with depth. Besides top layers, denitrifying genes (nosZ) were also present at depth, indicating a higher denitrification potential in the deeper layers. However, these results contrasted with in situ denitrification enzyme assay (DEA) measurements, suggesting the presence of dormant microbes and/or other nitrogen processes in deep sediments that compete with denitrification. In addition to enhanced depth stratification, our results also highlighted that dam removal increased species richness, microbial diversity, and nitrification. DISCUSSION: Lateral and vertical spatial distributions of soil microbiomes (both prokaryotes and fungi) suggest that not only sediment stratification but also concurrent watershed conditions are important in explaining the depth profiles of microbial communities and functional genes in dammed rivers. The results also provide valuable information and guidance to stakeholders and restoration projects. Frontiers Media S.A. 2023-06-29 /pmc/articles/PMC10339028/ /pubmed/37455732 http://dx.doi.org/10.3389/fmicb.2023.1161043 Text en Copyright © 2023 Kan, Peck, Zgleszewski, Peipoch and Inamdar. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Kan, Jinjun
Peck, Erin K.
Zgleszewski, Laura
Peipoch, Marc
Inamdar, Shreeram
Mill dams impact microbiome structure and depth distribution in riparian sediments
title Mill dams impact microbiome structure and depth distribution in riparian sediments
title_full Mill dams impact microbiome structure and depth distribution in riparian sediments
title_fullStr Mill dams impact microbiome structure and depth distribution in riparian sediments
title_full_unstemmed Mill dams impact microbiome structure and depth distribution in riparian sediments
title_short Mill dams impact microbiome structure and depth distribution in riparian sediments
title_sort mill dams impact microbiome structure and depth distribution in riparian sediments
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339028/
https://www.ncbi.nlm.nih.gov/pubmed/37455732
http://dx.doi.org/10.3389/fmicb.2023.1161043
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