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Distinguishing Iron‐Reducing from Sulfate‐Reducing Conditions
Author(s) -
Chapelle Francis H.,
Bradley Paul M.,
Thomas Mary Ann,
McMahon Peter B.
Publication year - 2009
Publication title -
groundwater
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.84
H-Index - 94
eISSN - 1745-6584
pISSN - 0017-467X
DOI - 10.1111/j.1745-6584.2008.00536.x
Subject(s) - ferrous , sulfate , chemistry , redox , sulfide , iron sulfate , solubility , environmental chemistry , inorganic chemistry , organic chemistry
Ground water systems dominated by iron‐ or sulfate‐reducing conditions may be distinguished by observing concentrations of dissolved iron (Fe 2+ ) and sulfide (sum of H 2 S, HS − , and S = species and denoted here as “H 2 S”). This approach is based on the observation that concentrations of Fe 2+ and H 2 S in ground water systems tend to be inversely related according to a hyperbolic function. That is, when Fe 2+ concentrations are high, H 2 S concentrations tend to be low and vice versa. This relation partly reflects the rapid reaction kinetics of Fe 2+ with H 2 S to produce relatively insoluble ferrous sulfides (FeS). This relation also reflects competition for organic substrates between the iron‐ and the sulfate‐reducing microorganisms that catalyze the production of Fe 2+ and H 2 S. These solubility and microbial constraints operate in tandem, resulting in the observed hyperbolic relation between Fe 2+ and H 2 S concentrations. Concentrations of redox indicators, including dissolved hydrogen (H 2 ) measured in a shallow aquifer in Hanahan, South Carolina, suggest that if the Fe 2+ /H 2 S mass ratio (units of mg/L) exceeded 10, the screened interval being tapped was consistently iron reducing (H 2 ∼0.2 to 0.8 nM). Conversely, if the Fe 2+ /H 2 S ratio was less than 0.30, consistent sulfate‐reducing (H 2 ∼1 to 5 nM) conditions were observed over time. Concomitantly high Fe 2+ and H 2 S concentrations were associated with H 2 concentrations that varied between 0.2 and 5.0 nM over time, suggesting mixing of water from adjacent iron‐ and sulfate‐reducing zones or concomitant iron and sulfate reduction under nonelectron donor–limited conditions. These observations suggest that Fe 2+ /H 2 S mass ratios may provide useful information concerning the occurrence and distribution of iron and sulfate reduction in ground water systems.