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Deciphering and Predicting Spatial and Temporal Concentrations of Arsenic Within the Mekong Delta Aquifer

机译:湄公河三角洲含水层中砷的时空浓度的破译和预测

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摘要

Unravelling the complex, coupled processes responsible for the spatial distribution of arsenic within groundwaters of South and South-East Asia remains challenging, limiting the ability to predict the subsurface spatial distribution of arsenic. Previous work illustrates that Himalayan-derived, near-surface (0 to 12 m) sediments contribute a substantial quantity of arsenic to groundwater, and that desorption from the soils and sediments is driven by the reduction of AsV and arsenic-bearing iron (hydr)oxides. However, the complexities of groundwater flow will ultimately dictate the distribution of arsenic within the aquifer, and these patterns will be influenced by inherent physical heterogeneity along with human alterations of the aquifer system. Accordingly, we present a unified biogeochemical and hydrologic description of arsenic release to the subsurface environment of an arsenic-afflicted aquifer in the Mekong Delta, Kandal Province, Cambodia, constructed from measured geochemical profiles and hydrologic parameters. Based on these measurements, we developed a simple yet dynamic reactive transport model to simulate one- and two-dimensional geochemical profiles of the near surface and aquifer environment to examine the effects of subsurface physical variation on the distribution of arsenic. Our results show that near-surface release (0–12 m) contributes enough arsenic to the aquifer to account for observed field values and that the spatial distribution of arsenic within the aquifer is strongly affected by variations in biogeochemical and physical parameters. Furthermore, infiltrating dissolved organic carbon and ample buried particulate organic carbon ensures arsenic release from iron (hydr)oxides will occur for hundreds to thousands of years.
机译:弄清造成南亚和东南亚地下水内砷空间分布的复杂,耦合过程仍然具有挑战性,限制了预测砷地下空间分布的能力。先前的工作表明,喜马拉雅山近地表沉积物(0到12 m)对地下水贡献了大量砷,而土壤和沉积物的解吸是由AsV和含砷铁(水合物)的减少驱动的。氧化物。但是,地下水流动的复杂性最终决定了含水层中砷的分布,这些模式将受到固有的物理异质性以及人为改变含水层系统的影响。因此,我们根据测量的地球化学特征和水文参数,提出了一个统一的生物地球化学和水文描述,将砷释放到柬埔寨坎达尔省湄公河三角洲受砷影响的含水层的地下环境中。基于这些测量,我们开发了一个简单而动态的反应性输运模型,以模拟近地表和含水层环境的一维和二维地球化学剖面,以研究地下物理变化对砷分布的影响。我们的结果表明,近地表释放(0–12 m)为含水层贡献了足够的砷,足以说明观测到的场值,而且生物地球化学和物理参数的变化强烈影响含水层中砷的空间分布。此外,渗透溶解的有机碳和充足的被掩埋的颗粒状有机碳可确保砷从铁氧化物中释放出数百至数千年的历史。

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