Published July 15, 2017 | Version v1
Journal article

High resolution profile of inorganic aqueous geochemistry and key redox zones in an arsenic bearing aquifer in Cambodia

  • 1. School of Earth and Environmental Sciences and Williamson Research Centre for Molecular Environmental Science, The University of Manchester, Williamson Building, Oxford Road, Manchester M13 9PL (United Kingdom)
  • 2. Department of Environmental Science, Royal University of Phnom Penh, Phnom Penh (Cambodia)
  • 3. Faculty of Agricultural Economics and Rural Development, Royal University of Agriculture, Phnom Penh (Cambodia)
  • 4. ETH Zurich, Institute of Geophysics, Sonneggstrasse 5, 8092 Zurich (Switzerland)
  • 5. British Geological Survey, Environmental Science Centre, Keyworth, Nottingham NG12 5GG (United Kingdom)
  • 6. Department of Earth Sciences, University of Oxford, South Parks Road, Oxford OX1 3AN (United Kingdom)

Description

Arsenic contamination of groundwaters in South and Southeast Asia is a major threat to public health. In order to better understand the geochemical controls on the mobility of arsenic in a heavily arsenic-affected aquifer in northern Kandal Province, Cambodia, key changes in inorganic aqueous geochemistry have been monitored at high vertical and lateral resolution along dominant groundwater flow paths along two distinct transects. The two transects are characterized by differing geochemical, hydrological and lithological conditions. Arsenic concentrations in groundwater are highly heterogenous, and are broadly positively associated with iron and negatively associated with sulfate and dissolved oxygen. The observed correlations are generally consistent with arsenic mobilization by reductive-dissolution of iron (hydr)oxides. Key redox zones, as identified using groupings of the PHREEQC model equilibrium electron activity of major redox couples (notably ammonium/nitrite; ammonium/nitrate; nitrite/nitrate; dissolved oxygen/water) have been identified and vary with depth, site and season. Mineral saturation is also characterized. Seasonal changes in groundwater chemistry were observed in areas which were (i) sandy and of high permeability; (ii) in close proximity to rivers; and/or (iii) in close proximity to ponds. Such changes are attributed to monsoonal-driven surface-groundwater interactions and are consistent with the separate provenance of recharge sources as identified using stable isotope mixing models. - Highlights: • Key changes in inorganic aqueous geochemistry monitored at high spatial resolution. • Groundwater arsenic is highly heterogeneous and often exceeds health guidelines. • Arsenic associated with iron, sulfate and dissolved oxygen along natural flowpaths. • Geochemical models used to determine model redox equilibrium and mineral saturation. • Key characterized aquifer redox zones can vary with depth, lithology, site & season.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.scitotenv.2017.02.217

Additional details

Identifiers

DOI
10.1016/j.scitotenv.2017.02.217;
PII
S0048-9697(17)30482-5;

Publishing Information

Journal Title
Science of the Total Environment
Journal Volume
590-591
Journal Page Range
p. 540-553
ISSN
0048-9697
CODEN
STENDL

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.