High-Arsenic Groundwater in Paleochannels of the Lower Yellow River, China: Distribution and Genesis Mechanisms

High-arsenic (As) groundwater poses a serious threat to human health. The upper and middle reaches of the Yellow River are well-known areas for the enrichment of high-arsenic groundwater. However, little is known about the distribution characteristics and formation mechanism of high-As groundwater in the lower reach of the Yellow River. There were 203 groundwater samples collected in different groundwater systems of the lower Yellow River for the exploration of its hydrogeochemical characteristics. Results showed that more than 20% of the samples have arsenic concentrations exceeding 10 mu g/L. The high-As groundwater was mainly distributed in Late Pleistocene-Holocene aquifers, and the As concentrations in the paleochannels systems (C2 and C4) were significantly higher than that of the paleointerfluve system (C3) and modern Yellow River affected system (C5). The high-As groundwater is characterized by high Fe2+ and NH4+ and low Eh and NO3-, indicating that reductive dissolution of the As-bearing iron oxides is probably the main cause of As release. The arsenic concentrations strikingly showed an increasing tendency as the HCO3- proportion increases, suggesting that HCO3- competitive adsorption may facilitate As mobilization, too. In addition, a Gibbs diagram showed that the evaporation of groundwater could be another significant hydrogeochemical processes, except for the water-rock interaction in the study area. Different sources of aquifer medium and sedimentary structure may be the main reasons for the significant zonation of the As spatial distribution in the lower Yellow River.

Automated summary

High-arsenic groundwater poses a serious threat to human health, with concentrations exceeding 10μg/L in over 20% of samples in the lower Yellow River area. The distribution is mainly in Late Pleistocene-Holocene aquifers, with significantly higher concentrations in paleochannel systems. The main cause of As release is likely the reductive dissolution of As-bearing iron oxides.