TY - JOUR
T1 - Modeling non-steady state radioisotope transport in the vadose zone - A case study using uranium isotopes at Peña Blanca, Mexico
AU - Ku, T. L.
AU - Luo, S.
AU - Goldstein, S. J.
AU - Murrell, M. T.
AU - Chu, W. L.
AU - Dobson, P. F.
N1 - Funding Information:
We thank Schon Levy, Ardith Simmons, and Ron Oliver of LANL for valuable assistance and inputs at various stages of the research. We also thank Paul Cook of LBNL and our Universidad Autónoma de Chihuahua colleagues for their help in sample collection. The US Department of Energy’s Office of Civilian Radioactive Waste Management (OCRWM) provided financial support (DE-AC02-05CH11231). The views expressed in this paper do not necessarily reflect those of OCRWM. Our presentation is substantially improved by comments made by Ian Bourg, William M. Murphy and an anonymous reviewer. This work is dedicated to the late Miro Ivanovich who had contributed so much to the field.
PY - 2009/10/15
Y1 - 2009/10/15
N2 - Current models using U- and Th-series disequilibria to study radioisotope transport in groundwater systems mostly consider a steady-state situation. These models have limited applicability to the vadose zone (UZ) where the concentration and migratory behavior of radioisotopes in fluid are often transitory. We present here, as a first attempt of its kind, a model simulating the non-steady state, intermittent fluid transport in vadose layers. It provides quantitative constraints on in-situ migration of dissolved and colloidal radioisotopes in terms of retardation factor and rock-water interaction (or water transit) time. For uranium, the simulation predicts that intermittent flushing in the UZ leads to a linear relationship between reciprocal U concentration and 234U/238U ratio in percolating waters, with the intercept and slope bearing information on the rates of dissolution and α-recoil of U isotopes, respectively. The general validity of the model appears to be borne out by the measurement of uranium isotopes in UZ waters collected at various times over a period during 1995-2006 from a site in the Peña Blanca mining district, Mexico, where the Nopal I uranium deposit is located. Enhanced 234U/238U ratios in vadose-zone waters resulting from lengthened non-flushing time as prescribed by the model provide an interpretative basis for using 234U/238U in cave calcites to reconstruct the regional changes in hydrology and climate. We also provide a theoretical account of the model's potential applications using radium isotopes.
AB - Current models using U- and Th-series disequilibria to study radioisotope transport in groundwater systems mostly consider a steady-state situation. These models have limited applicability to the vadose zone (UZ) where the concentration and migratory behavior of radioisotopes in fluid are often transitory. We present here, as a first attempt of its kind, a model simulating the non-steady state, intermittent fluid transport in vadose layers. It provides quantitative constraints on in-situ migration of dissolved and colloidal radioisotopes in terms of retardation factor and rock-water interaction (or water transit) time. For uranium, the simulation predicts that intermittent flushing in the UZ leads to a linear relationship between reciprocal U concentration and 234U/238U ratio in percolating waters, with the intercept and slope bearing information on the rates of dissolution and α-recoil of U isotopes, respectively. The general validity of the model appears to be borne out by the measurement of uranium isotopes in UZ waters collected at various times over a period during 1995-2006 from a site in the Peña Blanca mining district, Mexico, where the Nopal I uranium deposit is located. Enhanced 234U/238U ratios in vadose-zone waters resulting from lengthened non-flushing time as prescribed by the model provide an interpretative basis for using 234U/238U in cave calcites to reconstruct the regional changes in hydrology and climate. We also provide a theoretical account of the model's potential applications using radium isotopes.
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U2 - 10.1016/j.gca.2009.07.011
DO - 10.1016/j.gca.2009.07.011
M3 - Article
AN - SCOPUS:69849102142
SN - 0016-7037
VL - 73
SP - 6052
EP - 6064
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
IS - 20
ER -