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- W2040300511 abstract "It is the purpose of this study to demonstrate that the molecular scale reaction mechanisms describing calcite precipitation and calcium isotope fractionations under highly controlled laboratory conditions also reproduce field scale measurements of δ44Ca in groundwater systems. We present data collected from an aquifer during active carbonate mineral precipitation and develop a reactive transport model capturing the observed chemical and isotopic variations. Carbonate mineral precipitation and associated fluid δ44Ca data were measured in multiple clogged well bores during organic carbon amended biogenic reduction of a uranium contaminated aquifer in western Colorado, USA. Secondary mineral formation induced by carbonate alkalinity generated during the biostimulation process lead to substantial permeability reduction in multiple electron-donor injection wells at the field site. These conditions resulted in removal of aqueous calcium from a background concentration of 6 mM to <1 mM while δ44Ca enrichment ranged from 1‰ to greater than 2.5‰. The relationship between aqueous calcium removal and isotopic enrichment did not conform to Rayleigh model behavior. Explicit treatment of the individual isotopes of calcium within the CrunchFlow reactive transport code demonstrates that the system did not achieve isotopic reequilibration over the time scale of sample collection. Measured fluid δ44Ca values are accurately reproduced by a linear rate law when the Ca2+:CO32− activity ratio remains substantially greater than unity. Variation in the measured δ44Ca between wells is shown to originate from a difference in carbonate alkalinity generated in each well bore. The influence of fluid Ca2+:CO32− ratio on the precipitation rate and δ44Ca is modeled by coupling the CrunchFlow reactive transport code to an ion by ion growth model. This study presents the first coupled ion-by-ion and reactive transport model for isotopic enrichment and demonstrates that reproducing field-scale δ44Ca enrichment in groundwater where Ca2+:CO32− approaches unity is only accomplished by utilizing such a coupled modeling approach." @default.
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- W2040300511 date "2013-10-01" @default.
- W2040300511 modified "2023-10-15" @default.
- W2040300511 title "Calcium isotope fractionation in groundwater: Molecular scale processes influencing field scale behavior" @default.
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- W2040300511 doi "https://doi.org/10.1016/j.gca.2013.05.022" @default.
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