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  • 1
    Publication Date: 2022-12-06
    Description: Molecular‐biological data and omics tools have increasingly been used to characterize microorganisms responsible for the turnover of reactive compounds in the environment, such as reactive‐nitrogen species in groundwater. While transcripts of functional genes and enzymes are used as measures of microbial activity, it is not yet clear how they are quantitatively related to actual turnover rates under variable environmental conditions. As an example application, we consider the interface between rivers and groundwater which has been identified as a key driver for the turnover of reactive‐nitrogen compounds, that cause eutrophication of rivers and endanger drinking water production from groundwater. In the absence of measured data, we developed a reactive‐transport model for denitrification that simultaneously predicts the distributions of functional‐gene transcripts, enzymes, and reaction rates. Applying the model, we evaluate the response of transcripts and enzymes at the river‐groundwater interface to stable and dynamic hydrogeochemical regimes. While functional‐gene transcripts respond to short‐term (diurnal) fluctuations of substrate availability and oxygen concentrations, enzyme concentrations are stable over such time scales. The presence of functional‐gene transcripts and enzymes globally coincides with the zones of active denitrification. However, transcript and enzyme concentrations do not directly translate into denitrification rates in a quantitative way because of nonlinear effects and hysteresis caused by variable substrate availability and oxygen inhibition. Based on our simulations, we suggest that molecular‐biological data should be combined with aqueous geochemical data, which can typically be obtained at higher spatial and temporal resolution, to parameterize and calibrate reactive‐transport models.
    Description: Plain Language Summary: Molecular‐biological tools can detect how many enzymes, functional genes, and gene transcripts (i.e., precursors of enzyme production) associated with a microbial reaction exist in a sample from the environment. Although these measurements contain valuable information about the number of bacteria and how active they are, they do not directly say how quickly a contaminant like nitrate disappears. Nitrate, from agriculture and other sources, threatens groundwater quality and drinking water production. In the process of denitrification, bacteria can remove nitrate by converting it into harmless nitrogen gas using specialized enzymes. The interface between rivers and groundwater is known as a place where denitrification takes place. In this study, we use a computational model to simulate the coupled dynamics of denitrification, bacteria, transcripts, and enzymes when nitrate‐rich groundwater interacts with a nearby river. The simulations yield complex and nonunique relationships between the denitrification rates and the molecular‐biological variables. While functional‐gene transcripts respond to daily fluctuations of environmental conditions, enzyme concentrations and genes are stable over such time scales. High levels of functional‐gene transcripts therefore provide a good qualitative indicator of reactive zones. Quantitative predictions of nitrate turnover, however, will require high‐resolution measurements of the reacting compounds, genes, and transcripts.
    Description: Key Points: We simulate the distributions of functional‐gene transcripts and enzymes related to denitrification at the river‐groundwater interface. Functional‐gene transcripts respond quickly to diurnal fluctuations of substrate and oxygen concentrations. Substrate limitation and oxygen inhibition impede the direct prediction of denitrification rates from transcript or enzyme concentrations.
    Description: Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659
    Description: https://doi.org/10.5281/zenodo.6584591
    Description: https://gitlab.com/astoeriko/nitrogene
    Description: https://doi.org/10.5281/zenodo.6584641
    Description: https://gitlab.com/astoeriko/adrpy
    Description: https://doi.org/10.5281/zenodo.5213947
    Description: https://github.com/aseyboldt/sunode
    Keywords: ddc:551 ; reactive‐transport modeling ; denitrification ; groundwater‐river interface ; functional genes ; transcripts ; molecular biology
    Language: English
    Type: doc-type:article
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  • 2
    Publication Date: 2021-07-03
    Description: Spectral induced polarization signatures have been used as proxies for microbial abundance in subsurface environments, by taking advantage of the charged properties of microbial cell membranes. The method's applicability, however, remains qualitative, and signal interpretation ambiguous. The adoption of spectral induced polarization as a robust geo‐microbiological tool for monitoring microbial dynamics in porous media requires the development of quantitative relationships between biogeochemical targets and spectral induced polarization parameters, such as biomass density and imaginary conductivity (σ″). Furthermore, deriving cell density information from electrical signals in porous media necessitates a detailed understanding of the nature of the cell membrane surface charge dynamics. We present results from a fully saturated sand‐filled column reactor experiment where Shewanella oneidensis growth during nitrate reduction to ammonium was monitored using spectral induced polarization. While our results further confirm the direct dependence of σ″ on changing cell density, Cole–Cole derived relaxation times also record the changing surface charging properties of the cells, ascribed to toxic stress due to nitrite accumulation. Concurrent estimates of cell size yield the first measurement‐derived estimation of the apparent surface ion diffusion coefficient for cells (Ds = 5.4 ±1.3 µm2 s−1), strengthening the link between spectral induced polarization and electrochemical cell polarization. Our analysis provides a theoretical framework on which to build σ″–cell density relations using bench‐scale experiments, leading to eventual robust non‐destructive monitoring of in situ microbial growth dynamics.
    Description: Canada Excellence Research Chair programme
    Description: Waterloo‐Technion University Cooperation Programme
    Keywords: 622.15 ; Induced Polarization ; Environmental ; Shallow Subsurface
    Type: article
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