The Dynamics of the Concentration and Speciation of Arsenic in Private Drinking Water Wells in Eastern Wisconsin, USA

About 2.5 billion people rely on groundwater as their main drinking water source, and arsenic pollution within the groundwater system can cause serious short- and long-term health issues. Within the natural environment, arsenic generally exists as oxyanions which have two oxidation states, As(III) and As(V). Under ambient pH conditions, As(V) is primarily present as an anion (i.e., H2AsO4-) while As(III) tends to be uncharged (i.e., H3AsO3), making it much more difficult to remove As(III) through existing treatment techniques such as adsorption and reverse osmosis (RO). In Eastern Wisconsin, the dolomite and dolomite/sandstone aquifers represent a major drinking water source and high arsenic concentrations have been observed. Previous studies showed that arsenic can be released into private drinking water wells due to the oxidation of sulfide-bearing minerals with arsenic impurities that are usually dispersed within the dolomite and sandstone bedrock. However, there is a lack of information on the concentrations of each arsenic species as well as arsenic dynamics during water pumping/usage. The primary goals of this research were (1) to quantify the baseline concentrations of each arsenic species within selected Eastern Wisconsin private drinking water wells, and (2) to determine how the arsenic concentrations and species could be affected by continuous water usage. Our results showed that As(III) was the dominant species of arsenic, and during continuous water usage, there could be an upward trend in arsenic concentration (there was minimal change in arsenic speciation). Upon the completion of water pumping, arsenic concentrations decreased over time and returned to pre-pumping levels. Our findings highlighted the importance of quantifying the speciation and dynamics of arsenic during water use to the assessment of public health risks and the design of appropriate water treatment techniques.