Jung Hun Bok, Zheng Yan, Rahman Mohammad W, Rahman Mohammad M, Ahmed Kazi M
School of Earth and Environmental Sciences, Queens College and the Graduate School and University Center, The City University of New York, Flushing, New York 11367, USA.
School of Earth and Environmental Sciences, Queens College and the Graduate School and University Center, The City University of New York, Flushing, New York 11367, USA; Lamont-Doherty Earth Observatory of Columbia University, 61 Route 9W, Palisades, New York 10964, USA.
Appl Geochem. 2015 Dec 1;63:647-660. doi: 10.1016/j.apgeochem.2015.09.001.
Riverbank sediment cores and pore waters, shallow well waters, seepage waters and river waters were collected along the Meghna Riverbank in Gazaria Upazila, Bangladesh in Jan. 2006 and Oct.-Nov. 2007 to investigate hydrogeochemical processes controlling the fate of groundwater As during discharge. Redox transition zones from suboxic (0-2 m depth) to reducing (2-5 m depth) then suboxic conditions (5-7 m depth) exist at sites with sandy surficial deposits, as evidenced by depth profiles of pore water (n=7) and sediment (n=11; diffuse reflectance, Fe(III)/Fe ratios and Fe(III) concentrations). The sediment As enrichment zone (up to 700 mg kg) is associated with the suboxic zones mostly between 0-2 m depth and less frequently between 5-7 m depth. The As enriched zones consist of several 5 to 10 cm-thick dispersed layers and span a length of ~5-15 m horizontally from the river shore. Depth profiles of riverbank pore water deployed along a 32 m transect perpendicular to the river shore show elevated levels of dissolved Fe (11.6±11.7 mg L) and As (118±91 μg L, mostly as arsenite) between 2-5 m depth, but lower concentrations between 0-2 m depth (0.13±0.19 mg L Fe, 1±1 μg L As) and between 5-6 m depth (1.14±0.45 mg L Fe, 28±17 μg L As). Because it would take more than a few hundred years of steady groundwater discharge (10 m yr) to accumulate hundreds of mg kg of As in the riverbank sediment, it is concluded that groundwater As must have been naturally elevated prior to anthropogenic pumping of the aquifer since the 1970s. Not only does this lend unequivocal support to the argument that As occurrence in the Ganges-Brahmaputra-Meghna Delta groundwater is of geogenic origin, it also calls attention to the fate of this As enriched sediment as it may recycle As into the aquifer.
2006年1月以及2007年10月至11月期间,在孟加拉国加扎里亚乌帕齐拉的梅克纳河岸采集了河岸沉积物岩芯及孔隙水、浅井水、渗流水和河水,以研究控制地下水砷在排放过程中归宿的水文地球化学过程。在具有砂质表层沉积物的地点存在从亚缺氧(0 - 2米深度)到还原(2 - 5米深度)再到亚缺氧条件(5 - 7米深度)的氧化还原过渡带,孔隙水(n = 7)和沉积物(n = 11;漫反射、铁(III)/铁比率和铁(III)浓度)的深度剖面证明了这一点。沉积物砷富集区(高达约700毫克/千克)主要与0 - 2米深度之间的亚缺氧带相关,较少与5 - 7米深度之间的亚缺氧带相关。砷富集区由几个5至10厘米厚的分散层组成,从河岸水平延伸约5 - 15米。沿着垂直于河岸的32米断面布置的河岸孔隙水深度剖面显示,在2 - 5米深度之间溶解铁(11.6±11.7毫克/升)和砷(118±91微克/升,主要为亚砷酸盐)含量升高,但在0 - 2米深度(0.13±0.19毫克/升铁,1±1微克/升砷)和5 - 6米深度(1.14±0.45毫克/升铁,28±17微克/升砷)之间浓度较低。由于在河岸沉积物中积累数百毫克/千克的砷需要数百年稳定的地下水排放(约10米/年),因此得出结论,自20世纪70年代以来人为抽取含水层之前,地下水中的砷必定已经自然升高。这不仅明确支持了恒河 - 布拉马普特拉 - 梅克纳三角洲地下水中砷的存在是地质成因的观点,还引起了人们对这种富含砷的沉积物归宿的关注,因为它可能会将砷再循环回含水层。