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孟加拉国三角洲沉积环境中地下水中的砷污染:一个自组织的复杂地球化学过程

Arsenic pollution in groundwater: a self-organizing complex geochemical process in the deltaic sedimentary environment, Bangladesh.

作者信息

Tareq Shafi M, Safiullah S, Anawar H M, Rahman M Majibur, Ishizuka T

机构信息

Division of Earth and Environmental Sciences, Graduate School of Environmental Studies, Nagoya University, Chikusa-ku, Nagoya 464-8601, Japan.

出版信息

Sci Total Environ. 2003 Sep 1;313(1-3):213-26. doi: 10.1016/S0048-9697(03)00266-3.

Abstract

The presence of considerable concentrations of As (Sonargon: below detection limit (bdl)-1.46 mg/l; Faridpur: bdl-1.66 mg/l) and some other elements (like B, F, U) in groundwater of the Ganges-Meghna-Brahmaputra (G-M-B) rivers flood plain indicate that several millions of people are consuming contaminated water. Conditions regulating the mobilization and diagenetic behavior of arsenic in sediments are not well characterized, although understanding these conditions is essential in order to predict the modes of transfer of this contaminant from sediments to groundwater. Analyses of vertical profiles of total arsenic and iron as well as easily soluble As and reducible (reactive) iron concentrations in sediments of the Ganges and Meghna flood plains show no arsenic-enriched layer up to 36-m depth. However, arsenic content in sediments is relatively higher than mean crustal concentration, showing some peaks (Sonargaon: 27.9 mg/kg; 3 m, 31.5 mg/kg; 9 m, 27.30 mg/kg; 16 m, 37.70 mg/kg; 29.5 m, Faridpur: 19.80 mg/kg; 6 m, 26.60 mg/kg; 14.5 m, 29.40 mg/kg; 25 m) depending on the periodical differences in sedimentary cycling of arsenic, metal (hydr)oxides and organic matter. Seasonal changes have no clear or consistent effect on the groundwater arsenic concentrations; with the exception of a small-scale localized irregular change (10-16%). However, easily reducible metal oxides and hydroxides were significant factors affecting the retention of arsenic by sediments during leaching. The biogeochemical cycling of arsenic and iron is closely coupled in deltaic systems where iron oxy-hydroxides provide a carrier phase for the deposition of arsenic in sediments. Analytical results of mimic leaching experiments strongly supported the reduction (Fe oxy-hydroxides) mechanism for arsenic mobilization in alluvial aquifer of deltaic sedimentary environment of G-M-B rivers flood plain.

摘要

恒河-梅克纳河-布拉马普特拉河(G-M-B)河漫滩的地下水中存在高浓度的砷(索纳贡:低于检测限(bdl)-1.46毫克/升;法里德布尔:bdl-1.66毫克/升)以及其他一些元素(如硼、氟、铀),这表明数百万人正在饮用受污染的水。尽管了解沉积物中砷的迁移和成岩行为的调控条件对于预测这种污染物从沉积物向地下水的转移方式至关重要,但目前对这些条件的特征描述尚不充分。对恒河和梅克纳河漫滩沉积物中总砷和铁的垂直剖面以及易溶性砷和可还原(活性)铁浓度的分析表明,在36米深度以内没有富砷层。然而,沉积物中的砷含量相对高于地壳平均浓度,并呈现出一些峰值(索纳贡:27.9毫克/千克;3米,31.5毫克/千克;9米,27.30毫克/千克;16米,37.70毫克/千克;29.5米,法里德布尔:19.80毫克/千克;6米,26.60毫克/千克;14.5米,29.40毫克/千克;25米),这取决于砷、金属(氢)氧化物和有机物沉积循环的周期性差异。季节性变化对地下水中的砷浓度没有明显或一致的影响;除了小规模的局部不规则变化(10%-16%)。然而,易还原的金属氧化物和氢氧化物是浸出过程中影响沉积物对砷保留的重要因素。在三角洲系统中,砷和铁的生物地球化学循环紧密耦合,其中铁的羟基氧化物为沉积物中砷的沉积提供了载体相。模拟浸出实验的分析结果有力地支持了G-M-B河漫滩三角洲沉积环境冲积含水层中砷迁移的还原(铁的羟基氧化物)机制。

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