Journal
ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 55, Issue 14, Pages 9876-9884Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c02049
Keywords
denitrification; siderite oxidation; NRFeOx; anoxic subsurface
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Funding
- Collaborative Research Center 1253 CAMPOS - German Research Foundation (DFG) [SFB 1253/1]
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Research indicates that direct microbial pyrite oxidation is a significant pathway in nitrate reduction, with enzymatic activity of the bacterial culture playing a key role, while the contribution of abiotic pyrite oxidation by Fe3+ is found to be negligible.
Neutrophilic microbial pyrite (FeS2) oxidation coupled to denitrilication is thought to be an important natural nitrate attenuation pathway in nitrate-contaminated aquifers. However, the poor solubility of pyrite raises questions about its bioavailability and the mechanisms underlying its oxidation. Here, we investigated direct microbial pyrite oxidation by a neutrophilic chemolithoautotrophic nitrate-reducing Fe(II)-oxidizing culture enriched from a pyrite-rich .aquifer. We used pyrite with natural abundance (NA) of Fe isotopes (NAFe-pyrite) and( 57)Fe-labeled siderite to evaluate whether the oxidation of the more soluble Fe(II)-carbonate (FeCO3) can indirectly drive abiotic pyrite oxidation. Our results showed that in setups where only pyrite was incubated with bacteria, direct microbial pyrite oxidation contributed ca. 26% to overall nitrate reduction. The rest was attributed to the oxidation of elemental sulfur (S-0), present as a residue from pyrite synthesis. Pyrite oxidation was evidenced in the NAFe-pyrite/Fe-57-siderite setups by maps of (FeO)-Fe-56 and S-32 obtained using a combination of SEM with nanoscale secondary ion MS (NanoSIMS), which showed the presence of Fe-56(III) (oxyhydr)oxides that could solely originate from (FeS2)-Fe-56. Based on the fit of a reaction model to the geochemical data and the Fe-isotope distributions from NanoSIMS, we conclude that anaerobic oxidation of pyrite by our neutrophilic enrichment culture was mainly driven by direct enzymatic activity of the cells. The contribution of abiotic pyrite oxidation by Fe3+ appeared to be negligible in our experimental setup.
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