首页> 外文期刊>Journal of Hydrology >Unraveling influences of nitrogen cycling on arsenic enrichment in groundwater from the Hetao Basin using geochemical and multi-isotopic approaches
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Unraveling influences of nitrogen cycling on arsenic enrichment in groundwater from the Hetao Basin using geochemical and multi-isotopic approaches

机译:利用地球化学和多同位素方法解开氮盆地地下水中砷富集的砷富集的影响

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Sources and co-cycling of nitrogen species in arsenic-prone groundwater remain poorly understood, which could affect arsenic behavior. Here, geochemical and multi-isotopic characteristics of groundwater from various redox environments were investigated to reveal the effects of nitrogen cycling on arsenic mobility in groundwater systems from the Hetao Basin in China. In deep groundwater along an approximate flow path from the alluvial fan (Zone I) through the transition area (Zone II) and to the flat plain (Zone III), a progressive NO3- depletion with gradually increased delta N-15(NO3) and delta O-18(NO3) occurred, accompanied by increases in dissolved NH4+, Fe(II), and arsenic concentrations and a decrease in delta N-15(NH4). Shallow groundwater in the flat plain (Zone IV) covered wider ranges of delta N-15(NO3) and delta O-18(NO3) and relatively lower delta N-15(NH4). Organic nitrogen mineralization contributed primarily to NH4+ release in all zones, and dissimilatory NO3- reduction to NH4+ (DNRA) was an important NH4+ source in Zone IV. While NH4+ loss mainly occurred via nitrification in Zone I, anaerobic NH4+ oxidation was coupled to Fe(III) oxide reduction (Feammox) in Zones II and III and to NO2- reduction (anammox) in Zones II, III, and IV. Groundwater NO3- was reduced via heterotrophic denitrification in Zones II and III, while the DNRA was favored over denitrification in Zone IV with much higher DOC:NO3- molar ratios. Feammox and heterotrophic DNRA increased the dissolved Fe(II) and arsenic concentrations via the enhanced Fe(III) oxide reduction. However, anammox and Fe(II)-fueled autotrophic DNRA decreased their concentrations due to limited Fe(III) oxide reduction and/or enhanced Fe(II) oxidation. The influences of nitrogen cycling on arsenic behavior are mainly mediated by transformations between Fe(III) oxides and dissolved Fe(II). This study provides the first detailed multi-isotopic picture of nitrogen cycling and the relevant effects on arsenic enrichment processes.
机译:易砷地下水中氮物种的来源和共循环仍不清楚,这可能会影响砷的行为。本文研究了不同氧化还原环境地下水的地球化学和多同位素特征,揭示了氮循环对中国河套盆地地下水系统砷迁移的影响。在从冲积扇(I区)到过渡区(II区)再到平原(III区)的大致流动路径沿线的深层地下水中,出现了一种逐渐增加的N-15(NO3)和O-18(NO3)增量的NO3-消耗,伴随着溶解NH4+、Fe(II)和砷浓度的增加,以及N-15(NH4)增量的降低。平坦平原(IV区)的浅层地下水覆盖范围更广的三角洲N-15(NO3)和三角洲O-18(NO3)以及相对较低的三角洲N-15(NH4)。有机氮矿化主要有助于所有区域的NH4+释放,而异化NO3-还原为NH4+(DNRA)是IV区的一个重要NH4+来源。虽然NH4+的损失主要通过I区的硝化作用发生,但厌氧NH4+氧化与II区和III区的铁(III)氧化物还原(FeAmox)以及II区、III区的NO2-还原(Anamox)耦合,在II区和III区,地下水NO3-通过异养反硝化作用减少,而在DOC:NO3-摩尔比高得多的IV区,DNRA优于反硝化作用。Feammox和异养DNRA通过增强的Fe(III)氧化物还原增加溶解的Fe(II)和砷浓度。然而,由于有限的Fe(III)氧化物还原和/或增强的Fe(II)氧化,厌氧氨氧化和以Fe(II)为燃料的自养DNRA降低了它们的浓度。氮循环对砷行为的影响主要通过Fe(III)氧化物和溶解的Fe(II)之间的转化来实现。这项研究首次提供了氮循环的详细多同位素图像,以及对砷富集过程的相关影响。

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