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Temporal variability of groundwater chemistry in shallow and deep aquifers of Araihazar, Bangladesh

机译:孟加拉国阿拉伊哈扎尔浅层和深层含水层中地下水化学的时间变异性

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Samples were collected every 2-4 weeks from a set of 37 monitoring wells over a period of 2-3 years in Araihazar, Bangladesh, to evaluate the temporal variability of groundwater composition for As and other constituents. The monitoring wells are grouped in 6 nests and span the 5-91 m depth range. Concentrations of As, Ca, Fe, K, Mg, Mn, Na, P, and S were measured by high-resolution ICPMS with a precision of 5% or better; concentrations of Cl were measured by ion chromatography. In shallow wells <30 m deep, As and P concentrations generally varied by <30%, whereas concentrations of the major ions (Na, K, Mg, Ca and Cl) and the redox-sensitive elements (Fe, Mn, and S) varied over time by up to ±90%. In wells tapping the deeper aquifers >30 m often below clay layers concentrations of groundwater As were much lower and varied by <10%. The concentrations of major cations also varied by <10% in these deep aquifers. In contrast, the concentration of redox-sensitive constituents Fe, S, and Mn in deep aquifers varied by up to 97% over time. Thus, strong decoupling between variations in As and Fe concentrations is evident in groundwaters from shallow and deep aquifers. Comparison of the time series data with groundwater ages determined by ~3H/~3He and ~(14)C dating shows that large seasonal or inter-annual variations in major cation and chloride concentrations are restricted to shallow aquifers and groundwater recharged <5 years ago. There is no corresponding change in As concentrations despite having significant variations of redox sensitive constituents in these very young waters. This is attributed to chemical buffering due to rapid equilibrium between solute and solid As. At two sites where the As content of groundwater in existing shallow wells averages 102 μg/L (range: < 5 to 648 μg/L; n = 118) and 272 μg/L (range: 10 to 485 μg/L; n=65), respectively, a systematic long-term decline in As concentrations lends support to the notion that flushing may slowly deplete an aquifer of As. Shallow aquifer water with >5 years ~3H/~3He age show a constant As:P molar ratio of 9.6 over time, suggesting common mechanisms of mobilization.
机译:每隔2-3年,每2-4周从孟加拉国Araihazar的37口监测井中收集一次样品,以评估As和其他成分的地下水组成随时间的变化。监测井分为6个巢穴,深度范围为5-91 m。砷,钙,铁,钾,镁,锰,钠,磷和硫的浓度通过高分辨率ICPMS进行测量,精度为5%或更高。通过离子色谱法测定Cl的浓度。在<30 m深的浅井中,As和P的浓度通常相差<30%,而主要离子(Na,K,Mg,Ca和Cl)和氧化还原敏感元素(Fe,Mn和S)的浓度随时间变化高达±90%。在水井中,经常在粘土层以下挖掘> 30 m的较深含水层,地下水As的浓度要低得多,变化幅度<10%。在这些深层含水层中,主要阳离子的浓度也相差<10%。相反,深层含水层中对氧化还原敏感的成分Fe,S和Mn的浓度随时间变化高达97%。因此,在浅层和深层含水层的地下水中,As和Fe浓度的变化之间存在很强的去耦关系。将时间序列数据与通过〜3H /〜3He和〜(14)C测年确定的地下水年龄进行比较,结果表明,主要阳离子和氯化物浓度的季节性或年际变化较大,仅限于浅层含水层,并且<5年前补给了地下水。尽管在这些非常年轻的水中氧化还原敏感成分有显着变化,但As浓度没有相应变化。这归因于溶质与固体As之间快速平衡的化学缓冲作用。在两个现有浅井中地下水的As含量平均值为102μg/ L(范围:<5至648μg/ L; n = 118)和272μg/ L(范围:10至485μg/ L; n = 65),砷浓度的系统性长期下降为潮冲可能会慢慢消耗砷含水层的观点提供了支持。年龄> 5H〜3H /〜3He年龄的浅层含水层水随着时间的推移显示出恒定的As:P摩尔比9.6,表明了普遍的动员机制。

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