School of Environmental Sciences, JNU, New Delhi, 67, India.
Environ Geochem Health. 2010 Apr;32(2):129-46. doi: 10.1007/s10653-009-9270-5. Epub 2009 Jun 24.
Arsenic contamination in groundwater is of increasing concern because of its high toxicity and widespread occurrence. This study is an effort to trace the factors responsible for arsenic enrichment in groundwater of the middle Gangetic Plain of India through major ion chemistry, arsenic speciation, sediment grain-size analyses, and multivariate statistical techniques. The study focuses on the distinction between the contributions of natural weathering and anthropogenic inputs of arsenic with its spatial distribution and seasonal variations in the plain of the state Bihar of India. Thirty-six groundwater and one sediment core samples were collected in the pre-monsoon and post-monsoon seasons. Various graphical plots and statistical analysis were carried out using chemical data to enable hydrochemical evaluation of the aquifer system based on the ionic constituents, water types, hydrochemical facies, and factors controlling groundwater quality. Results suggest that the groundwater is characterized by slightly alkaline pH with moderate to strong reducing nature. The general trend of various ions was found to be Ca(2+) > Na(+) > Mg(2+) > K(+) > NH(4) (+); and HCO(3) (-) > Cl(-) > SO(4) (2-) > NO(3) (-) > PO(4) (3-) > F(-) in both seasons. Spatial and temporal variations showed a slightly higher arsenic concentration in the pre-monsoon period (118 microg/L) than in the post-monsoon period (114 microg/L). Results of correlation analyses indicate that arsenic contamination is strongly associated with high concentrations of Fe, PO(4) (3-), and NH(4) (+) but relatively low Mn concentrations. Further, the enrichment of arsenic is more prevalent in the proximity of the Ganges River, indicating that fluvial input is the main source of arsenic. Grain size analyses of sediment core samples revealed clay (fine-grained) strata between 4.5 and 7.5 m deep that govern the vertical distribution of arsenic. The weathering of carbonate and silicate minerals along with surface-groundwater interactions, ion exchange, and anthropogenic activities seem to be the processes governing groundwater contamination, including with arsenic. Although the percentage of wells exceeding the permissible limit (50 microg/L) was less (47%) than that reported in Bangladesh and West Bengal, the percentage contribution of toxic As(III) to total arsenic concentration is quite high (66%). This study is vital considering that groundwater is the exclusive source of drinking water in the region and not only makes situation alarming but also calls for immediate attention.
地下水砷污染由于其高毒性和广泛存在而引起了越来越多的关注。本研究通过主要离子化学、砷形态、沉积物粒度分析和多元统计技术,努力追溯导致印度恒河中游平原地下水砷富集的因素。本研究侧重于区分自然风化和人为输入砷的贡献,以及它们在印度比哈尔邦平原的空间分布和季节性变化。在季风前和季风后季节采集了 36 个地下水和一个沉积物岩芯样本。使用化学数据进行各种图形绘制和统计分析,以使含水层系统的水化学评价基于离子成分、水类型、水化学相和控制地下水质量的因素。结果表明,地下水的 pH 值略呈碱性,具有中等至强还原性。在两个季节中,各种离子的总体趋势是 Ca(2+) > Na(+) > Mg(2+) > K(+) > NH(4) (+); HCO(3) (-) > Cl(-) > SO(4) (2-) > NO(3) (-) > PO(4) (3-) > F(-)。时空变化表明,季风前时期(118 微克/升)的砷浓度略高于季风后时期(114 微克/升)。相关分析结果表明,砷污染与 Fe、PO(4) (3-)和 NH(4) (+)的高浓度密切相关,但 Mn 浓度相对较低。此外,砷的富集在恒河附近更为普遍,表明河流输入是砷的主要来源。沉积物岩芯样本的粒度分析显示,在 4.5 至 7.5 米深处存在粘土(细粒)地层,控制着砷的垂直分布。碳酸盐和硅酸盐矿物的风化以及地表水-地下水相互作用、离子交换和人为活动似乎是控制地下水污染(包括砷污染)的过程。尽管超过允许限值(50 微克/升)的井的百分比(47%)低于孟加拉国和西孟加拉邦的报告,但有毒 As(III)对总砷浓度的百分比贡献相当高(66%)。考虑到地下水是该地区唯一的饮用水源,本研究至关重要,这不仅使情况令人担忧,而且还需要立即引起关注。