2022
DOI: 10.1016/j.scitotenv.2021.151930
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Unraveling the impact of iron oxides-organic matter complexes on iodine mobilization in alluvial-lacustrine aquifers from central Yangtze River Basin

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Cited by 16 publications
(16 citation statements)
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“…In aquifers, iodate and organic iodine are primarily bound to organic matter-rich iron minerals and thus microbially mediated reductive dissolution of iron minerals is believed to liberate the adsorbed iodine into groundwater. , Previous studies showed that SRB, such as Desulfovibrio vulgaris, Desulfovibrio putealis, and Desulfovibrio desulfuricans strain G-20, can not only biotically reduce iron oxides and clay minerals, but also perform chemical iron reduction through biogenic sulfide. Therefore, bacterial sulfate reduction in the deep confined high-iodine aquifers of the NCP may facilitate the reductive dissolution of iodine-bearing iron minerals and release adsorbed iodine into groundwater. This indirect iodine mobilization by bacterial sulfate reduction is similar to biogenic sulfide-driven arsenic mobilization in groundwater. , In addition, SRB could act directly on iodate reduction through sulfide-driven abiotic or enzymatic reactions.…”
Section: Discussionmentioning
confidence: 99%
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“…In aquifers, iodate and organic iodine are primarily bound to organic matter-rich iron minerals and thus microbially mediated reductive dissolution of iron minerals is believed to liberate the adsorbed iodine into groundwater. , Previous studies showed that SRB, such as Desulfovibrio vulgaris, Desulfovibrio putealis, and Desulfovibrio desulfuricans strain G-20, can not only biotically reduce iron oxides and clay minerals, but also perform chemical iron reduction through biogenic sulfide. Therefore, bacterial sulfate reduction in the deep confined high-iodine aquifers of the NCP may facilitate the reductive dissolution of iodine-bearing iron minerals and release adsorbed iodine into groundwater. This indirect iodine mobilization by bacterial sulfate reduction is similar to biogenic sulfide-driven arsenic mobilization in groundwater. , In addition, SRB could act directly on iodate reduction through sulfide-driven abiotic or enzymatic reactions.…”
Section: Discussionmentioning
confidence: 99%
“…Thermodynamically, iodide is the dominant species in reducing and weakly alkaline geogenic high-iodine groundwater, while iodate and organic iodine are mainly bound to aquifer sediments. , Given the low affinity of iodide to solid matrices, microbially mediated reduction of iodate is considered to be the main mechanism for iodide generation and enrichment in groundwater. To date, dissimilatory iodate-reducing bacteria and iron-reducing bacteria have been found to reduce iodate to iodide. For instance, dissimilatory iodate-reducing Denitromonas sp.…”
Section: Introductionmentioning
confidence: 99%
“…In addition to microbial iodate reduction, soluble ferrous iron, sulfide, and iron monosulfide were shown to reduce iodate to iodide abiotically . Based on the role of these strains and hydrogeochemical analysis, the reductions of iron and sulfate were proposed to play important roles in iodide mobilization in groundwater. ,,, However, this speculation has not been substantiated by the field observations. The functional roles of iodate-reducing, nitrate-reducing, iron-reducing, and sulfate-reducing microorganisms in iodine mobilization in aquifers are still unclear.…”
Section: Introductionmentioning
confidence: 99%
“…Many studies have confirmed that newly-formed amorphous iron (hydro) oxides preferentially bind phenolics and aromatic organic matter [ 11 , 13 , 30 , 31 , 32 ]. In addition, high molecular weight (MW > 500 Da) organic compounds and highly unsaturated or oxygen-rich organic matter (including polycyclic aromatic hydrocarbons, polyphenols, and carboxylic acid) have a higher affinity for iron (hydro) oxides [ 33 ].…”
Section: Introductionmentioning
confidence: 99%
“…The mechanism is that enzymatic polymerization transforms small molecular organic matter into larger molecule DOM with stronger iron affinity and then combines with iron ions to form Fe-OM through coprecipitation [ 34 , 35 ]. In general, organic matter with higher MW diffuse more slowly and have a stronger affinity for binding sites, while more minor MW organic matter tends to be more difficult to immobilize due to its weaker affinity [ 22 , 32 , 36 , 37 ]. At present, it is unclear how laccase-mediated Fe-OM affects the environmental behavior of metal(loid)s.…”
Section: Introductionmentioning
confidence: 99%