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首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Geochemical patterns of arsenic-enriched ground water in fractured, crystalline bedrock, Northport, Maine, USA
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Geochemical patterns of arsenic-enriched ground water in fractured, crystalline bedrock, Northport, Maine, USA

机译:美国缅因州诺斯波特的裂缝状结晶基岩中富含砷的地下水的地球化学特征

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摘要

High mean As concentrations of up to 26.6 mu mol/L (1990 mu g/L) occur in ground water collected from a fractured-bedrock system composed of sulfidic schist with granitic to dioritic intrusions. Sulfides in the bedrock are the primary source of the As in the ground water, but the presence of arsenopyrite in rock core retrieved from a borehole with As concentrations in the ground water barely above the detection limit of 2.0 mu mol/L, shows that there are complicating factors. Chemical analyses of water from 35 bedrock wells throughout a small watershed reveal spatial clustering of wells with high As concentrations. Stiff diagrams and box plots distinguish three distinct types; calcium-bicarbonate-dominated water with low As concentrations (CaHCO3 type), sodium-bicarbonate-dominated water with moderately high As concentrations (NaHCO3 type), and calcium-bicarbonate-dominated water with very high As concentrations (High-As type). It is proposed that differences in recharge area and ground-water evolution, and possible bedrock composition difference are responsible for the chemical distinctions within the watershed. Lack of correlation of As concentrations with pH indicates that desorption of As is an insignificant control on As concentration. Correlations of As concentrations with Fe and redox parameters indicates that reductive dissolution of Fe(III) oxyhydroxides may play a role in the occurrence of high As concentrations in the NaHCO3 and High-As type water. The oxidation of sulfide minerals occurs within the ground-water system and is ultimately responsible for the existence of As in the ground water, but there is no correlation between As and SO4 concentrations, probably due to precipitation of Fe(III) oxyhydroxides and adsorption of As under oxidizing conditions. Crown Copyright (c) 2006 Published by Elsevier Ltd. All rights reserved.
机译:从含硫片岩和花岗岩到闪长岩侵入体的裂缝性基岩系统收集的地下水中,最高平均砷浓度高达26.6μmol/ L(1990μg / L)。基岩中的硫化物是地下水中As的主要来源,但是从一个钻孔中回收的岩心中存在毒砂,而As中的As浓度仅略高于2.0μmol / L的检出限,表明是复杂的因素。在整个小流域中对35座基岩井中的水进行化学分析,发现高As浓度井的空间聚集。刚性图和箱形图将三种不同的类型区分开来。低砷浓度的碳酸氢钙为主的水(CaHCO3型),中等砷浓度的碳酸氢钠为主的水(NaHCO3型)和高砷浓度的碳酸氢钙为主的水(高砷型)。建议补给区和地下水演化的差异以及可能的基岩成分差异是造成流域内化学差异的原因。 As浓度与pH值缺乏相关性表明As的解吸对As浓度的影响微不足道。 As浓度与Fe和氧化还原参数之间的关系表明,Fe(III)羟基氧化铁的还原溶解可能在NaHCO3和High-As型水中高浓度的As发生中起作用。硫化物矿物的氧化发生在地下水系统中,并最终导致地下水中As的存在,但是As和SO4的浓度之间没有相关性,这可能是由于氢氧化三价铁(III)的沉淀和三氧化二铁的吸附所致。如在氧化条件下。 Crown版权所有(c)2006,由Elsevier Ltd.发行。保留所有权利。

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