TY - JOUR
T1 - Isotopic Fingerprint of Uranium Accumulation and Redox Cycling in Floodplains of the Upper Colorado River Basin
AU - Lefebvre, Pierre
AU - Noël, Vincent
AU - Lau, Kimberly V.
AU - Jemison, Noah E.
AU - Weaver, Karrie L.
AU - Williams, Kenneth H.
AU - Bargar, John R.
AU - Maher, Kate
N1 - Funding Information:
This research was supported by the DOE-BER Climate and Environmental Sciences Division through the SLAC Groundwater Quality Science Focus Area (SFA) program and by DOE-BES through its support for SSRL. SSRL and SLAC are supported by the DOE-BES under Contract No. DE-AC02-76SF00515. This material was partially supported by the Lawrence Berkeley National Laboratory’s Genomes-to-Watershed Scientific Focus Area that funded the work under contract DE-AC02-05CH11231 (Lawrence Berkeley National Laboratory; operated by the University of California). We thank the teams of U.S. DOE Office of Legacy Management and Environmental Sciences Laboratory of U.S. DOE Office at Grand Junction. We are very grateful to William Dam, Ray Johnson, and Sarah Morris for helping to manage the field sampling activities. The authors also thank Kristin Boye, Juan S. Lezama Pacheco, Emily Cardarelli, and Sharon Bone of SLAC National Accelerator Laboratory for their assistance with planning and conducting field sampling activities. We thank the SLAC radiation protection program for their assistance with radioactive sample handling and Guangchao Li (EM1 Laboratory, Stanford University) for his help during analyses by ICP-MS.
Publisher Copyright:
© Copyright 2019 American Chemical Society.
PY - 2019/4/2
Y1 - 2019/4/2
N2 - Uranium (U) groundwater contamination is a major concern at numerous former mining and milling sites across the Upper Colorado River Basin (UCRB), USA, where U(IV)-bearing solids have accumulated within naturally reduced zones (NRZs). Understanding the processes governing U reduction and oxidation within NRZs is critical for assessing the persistence of U in groundwater. To evaluate the redox cycling of uranium, we measured the U concentrations and isotopic compositions (δ 238 U) of sediments and pore waters from four study sites across the UCRB that span a gradient in sediment texture and composition. We observe that U accumulation occurs primarily within fine-grained (low-permeability) NRZs that show active redox variations. Low-permeability NRZs display high accumulation and low export of U, with internal redox cycling of U. In contrast, within high-permeability NRZs, U is remobilized under oxidative conditions, possibly without any fractionation, and transported outside the NRZs. The low δ 238 U of sediments outside of defined NRZs suggests that these reduced zones act as additional U sources. Collectively, our results indicate that fine-grained NRZs have a greater potential to retain uranium, whereas NRZs with higher permeability may constitute a more-persistent but dilute U source.
AB - Uranium (U) groundwater contamination is a major concern at numerous former mining and milling sites across the Upper Colorado River Basin (UCRB), USA, where U(IV)-bearing solids have accumulated within naturally reduced zones (NRZs). Understanding the processes governing U reduction and oxidation within NRZs is critical for assessing the persistence of U in groundwater. To evaluate the redox cycling of uranium, we measured the U concentrations and isotopic compositions (δ 238 U) of sediments and pore waters from four study sites across the UCRB that span a gradient in sediment texture and composition. We observe that U accumulation occurs primarily within fine-grained (low-permeability) NRZs that show active redox variations. Low-permeability NRZs display high accumulation and low export of U, with internal redox cycling of U. In contrast, within high-permeability NRZs, U is remobilized under oxidative conditions, possibly without any fractionation, and transported outside the NRZs. The low δ 238 U of sediments outside of defined NRZs suggests that these reduced zones act as additional U sources. Collectively, our results indicate that fine-grained NRZs have a greater potential to retain uranium, whereas NRZs with higher permeability may constitute a more-persistent but dilute U source.
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U2 - 10.1021/acs.est.8b05593
DO - 10.1021/acs.est.8b05593
M3 - Article
C2 - 30807121
AN - SCOPUS:85063088572
SN - 0013-936X
VL - 53
SP - 3399
EP - 3409
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 7
ER -