کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4698401 1637555 2015 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Arsenic solid-phase speciation in an alluvial aquifer system adjacent to the Himalayan forehills, Nepal
ترجمه فارسی عنوان
تجمع فاز جامد آرسنیک در یک سیستم آبخور آبرفتی در مجاورت هلیماهای هیمالیا، نپال
موضوعات مرتبط
مهندسی و علوم پایه علوم زمین و سیارات ژئوشیمی و پترولوژی
چکیده انگلیسی


• We use XAS to explore solid-phase As and Fe speciation along a topographic gradient at the upper-Ganges floodplain margin.
• There are clear trends in As speciation along the toposequence and with depth below ground surface.
• Discrete facies are enriched in As due to post-depositional diagenetic coupling between As and Fe mineralization.
• As(aq) in tube wells is more likely due to downward transport/desorption of As(III)-species.
• Landscape-scale controls on solid-phase As and Fe speciation in this region contrast with the lower Gangetic plain.

Alluvial aquifers contaminated by geogenic arsenic often lack direct solid-phase speciation data, hindering efforts to understand landscape-scale spatial heterogeneity and controls on As mobility. Here, we examine solid-phase As and Fe speciation of alluvial aquifer, river and hyporheic-seep sediments along a topographic gradient at the Himalayan foothills/upper-Ganges floodplain margin. We employ a combination of X-ray absorption spectroscopy, selective extracts, electron microscopy and X-ray fluorescence. Source-river sediments were found to contain a mixture of solid-phase As(V) and As(III) species, while vertically heterogeneous bore-hole sediments also contained a solid-phase As-sulfide species. In general, the abundance of reduced As species [As(III) + As-sulfide] increased with depth below ground surface, as well as down the topographic gradient from the foothills to the floodplain. Although Fe(III) oxides diminished with depth, goethite-rich nodules were present above the seasonal water table minima and contained 10–100 fold more As than the corresponding bulk sediments [~ 50–800 mg kg− 1; mainly As(V)]. In contrast, organic-rich clay layers below the seasonal water table contained abundant As-sulfide species (~ 30–80% of solid-phase As), as well as authigenic pyrite enriched in As [up to ~ 8500 mg kg− 1]. Results indicate that aquifer sediments contain discrete facies that are strongly enriched in As due to post-depositional diagenetic coupling between As retention and redox-dependent Fe mineralization. In riverine hyporheic-seeps, ferrihydrite traps As(V)/As(III) species (~ 30–200 mg kg− 1) in a readily exchangeable form, creating a pool of solid-phase As vulnerable to downstream reworking and subsequent reductive mobilization. A paucity of Fe(III) oxides in aquifer sediments at tube well-screen depth suggests that the abundant As(III)(aq) in floodplain tube wells is more likely attributable to downward transport or desorption of As(III)-species, than to contemporary reductive dissolution of As-bearing Fe oxides in sediments at well-screen depth. In contrast with the lower Gangetic plain, where large-scale floodplain sedimentary features are a key control on solid-phase As and Fe speciation, in these alluvial sediments solid-phase As and Fe speciation appears to be controlled mainly by physiographic properties (elevation; depth; seasonal water table) that influence local redox conditions.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemical Geology - Volume 419, 25 December 2015, Pages 55–66
نویسندگان
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