Arsenic in groundwater from Southwest Bangladesh: Sources, water quality, and potential health concern

Md. Shazzadur Rahman , A.H.M. Selim Reza , Md. Aminul Ahsan , Md. Abu Bakar Siddique
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Abstract

Arsenic (As) poisoning in groundwater has become one of the greatest environmental concerns around the world. In this study, As concentration in the groundwater samples (depth: 52–70 m) of southwestern Bangladesh was evaluated using Atomic Absorption Spectrometer (AAS) to know the current status, possible source(s), and probable health risk of As. In addition, the other relevant water quality parameters (pH, temperature, EC, TDS, Na+, K+, Ca2+, Mg2+, Cl, NO3, SO42−, HCO3, Fe, and Mn) were also measured using various instruments such as portable bench meter, Flame photometer, AAS, and Ion Chromatograph to evaluate the suitability of the water for drinking and irrigation purposes. Arsenic concentration (μg L−1) ranged from 13.10 to 292 (mean ± SD: 156.9 ± 100.31), which is alarmingly, and 15 times higher than the WHO recommended value for drinking water. pH values of collected groundwater samples ranged from 7.17 to 8.09, which exhibits a lightly alkaline nature. The average abundance of major cation follows the order of Ca2+ > Mg2+ > Na+ > K+, and the average abundance of major anions follows the order of HCO3 > Cl > NO3 > SO42−, with Ca2+and HCO3 being the dominant cation and anion, respectively. Based on water quality assessments utilizing the water quality index and entropy water quality index, the groundwater in the region of interest was not suitable for drinking or irrigation purposes. The Piper tri-linear diagram suggests the dominant water type in the study area was the Ca-HCO3 type, where Ca and HCO3 are the principal cations and anions, respectively. A bivariate analysis of different hydro-chemical parameters revealed that silicate weathering controls the hydrogeochemical processes in groundwater. Principal component and hierarchical cluster analysis indicate As in groundwater are geogenic in origin under reductive dissolution processes. The moderate correlation between As, Fe, and Mn indicate reductive dissolution of FeOOH and MnOOH plays a vital role in releasing As from sediment to groundwater. Probable cancer risk assessment for both adults and children revealed a higher value than the recommended value of 10−6 according to United Nations Environmental Protection Agency (USEPA), suggesting that people in the area of interest were at high carcinogenic risk.

孟加拉国西南部地下水中的砷:来源、水质和潜在的健康问题
地下水砷中毒已成为世界范围内最严重的环境问题之一。本研究利用原子吸收光谱仪(AAS)对孟加拉国西南部地下水样品(深度:52-70 m)中的砷浓度进行了评估,以了解砷的现状、可能的来源和可能的健康风险。此外,还使用便携式台架仪、火焰光度计、原子吸收光谱法和离子色谱仪等多种仪器测量了其他相关水质参数(pH、温度、EC、TDS、Na+、K+、Ca2+、Mg2+、Cl−、NO3−、SO42−、HCO3−、Fe和Mn),以评价饮用水和灌溉用水的适宜性。砷浓度(μg L−1)在13.10 ~ 292(平均值±SD: 156.9±100.31)之间,是令人担忧的,比世界卫生组织推荐的饮用水值高出15倍。采集的地下水pH值在7.17 ~ 8.09之间,呈浅碱性。主阳离子的平均丰度顺序为Ca2+ >Mg2 +比;Na +比;K+,主要阴离子的平均丰度顺序为:HCO3−>Cl−祝辞3号−祝辞SO42−,Ca2+和HCO3−分别为优势阳离子和阴离子。利用水质指数和熵水质指数对研究区水质进行评价,结果表明研究区地下水不适合饮用和灌溉。Piper三线性图显示,研究区主要的水类型为Ca-HCO3型,其中Ca和HCO3−分别是主要的阳离子和阴离子。对不同水化学参数的二元分析表明,硅酸盐风化控制着地下水的水文地球化学过程。主成分分析和层次聚类分析表明,地下水中的砷是在还原溶蚀作用下形成的。As、Fe和Mn之间的适度相关性表明,FeOOH和MnOOH的还原溶解在沉积物向地下水释放As中起着至关重要的作用。根据联合国环境保护署(USEPA)对成人和儿童进行的可能致癌风险评估显示,该数值高于推荐值10 - 6,这表明该地区的人们处于高致癌风险中。
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