首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >The origins of high concentrations of iron, sodium, bicarbonate, and arsenic in the Lower Mississippi River Alluvial Aquifer
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The origins of high concentrations of iron, sodium, bicarbonate, and arsenic in the Lower Mississippi River Alluvial Aquifer

机译:高浓度的铁,钠,碳酸氢盐和砷在密西西比河冲积含水层的起源

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摘要

Many alluvial aquifer systems are characterized in part by groundwater rich in sodium (Na) and bicarbonate (HCO3) and elevated concentrations of dissolved iron (Fe) and arsenic (As). However the relationships among Fe and As concentrations and the formation of Na-HCO3 waters are unclear. Here we evaluated the formation of Na-HCO3 groundwater in the Lower Mississippi River Alluvial Aquifer (LMRAA) in Louisiana, USA, where concentrations of dissolved Fe and As reached values as high as 16 mg/L and 64 mu g/L, respectively. Water isotope data showed that groundwater was predominantly recharged via local precipitation outboard of the Mississippi River, while groundwater nearer the river and to the south of the study area was more hydraulically connected to the river. Much of the geochemical data, including water isotopes, calcite saturation index, Na excess, and As correlated to some degree with well depth, highlighting the complex interactions between the shallower recharge from local precipitation and the deeper reaction pathways laterally connected to the Mississippi River and/or vertically connected with regional groundwater. The delta(13) C(DIC) of groundwater ranged from -17.4 to -11.1%o, likely representing a mixture of microbially- and abiotically-derived alkalinity. Within this context, the production of groundwater rich in Na-HCO3 can be explained by reaction pathways involving the weathering of Ca-Na silicate phases. This weathering, driven in part by the production of microbial CO3 during Fe and sulfate reduction, may continue past the point of calcite saturation. Once calcite reaches saturation the concentration of Ca is buffered, but there is a possibility of further buildup in the concentrations of Na and HCO3. The silicate weathering model serves as an alternative conceptual model to calcite dissolution and clay exchange for the development of Na-HCO3 waters. If globally important, this water-rock reaction pathway could place new constraints on the proces
机译:许多发生的含水层系统的特征在于富含钠(Na)和碳酸氢钠(HCO3)的地下水和溶解铁(Fe)和砷(AS)的浓度。然而,Fe和浓度之间的关系和Na-HCO3水的形成尚不清楚。在这里,我们评估了美国路易斯安那州的小密西西比河冲积含水层(LMRAA)的Na-HCO3地下水的形成,其中溶解的Fe浓度分别高达16mg / L和64μg/ L.水同位素数据显示地下水主要通过密西西比河的局部降水落地充电,而地下水更近的河流和研究区的南部更加液压连接到河流。大部分地球化学数据,包括水同位素,方解石饱和指数,Na过量,以及与深度良好的一定程度相关,突出浅沉淀之间的复杂相互作用,以及横向连接到密西西比河的更深的反应途径。 /或与区域地下水垂直连接。地下水的δ(13)C(DIC)从-17.4至-11.1%o的范围为-17.4至-11.1%o,可能代表微血上和无生物衍生的碱度的混合物。在这种情况下,可以通过涉及Ca-Na硅酸盐阶段的风化的反应途径来解释富含Na-HCO3的地下水的生产。这种风化,部分通过在Fe和硫酸盐期间产生微生物CO3和硫酸盐,可能会持续到方解石饱和点。一旦方解石达到饱和,就缓冲了Ca的浓度,但是在Na和HCO3的浓度下有可能进一步积聚。硅酸盐风化模型作为方便溶解和粘土交换的替代概念模型,用于纳 - HCO3水域的开发。如果全球重要的话,这种水摇滚反应途径可能对探头进行新的约束

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