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首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Distribution and reactivity of oxyanions (Sb, As, V, Mo) in the surface freshwater reaches of the Gironde Estuary (France)
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Distribution and reactivity of oxyanions (Sb, As, V, Mo) in the surface freshwater reaches of the Gironde Estuary (France)

机译:吉伦特河口(法国)地表淡水中含氧阴离子(Sb,As,V,Mo)的分布和反应性

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摘要

The present work reports on the temporal variations of Sb, As, V and Mo concentrations in the surface freshwater reaches of the Gironde Estuary (SW France). Dissolved (<0.2 and <0.02μm) and particulate Sb, As, V and Mo concentrations were measured in samples collected with high temporal resolution (every 30min) during two consecutive tides at a fixed station located upstream of the city of Bordeaux and the maximum turbidity zone (MTZ). In addition, measurements of suspended particulate matter concentration, physico-chemical parameters, Cl- concentration, water depth, current velocity and particulate Th concentration were performed either at the same time resolution or continuously. The data obtained suggested that variations in particulate As, V and Mo concentrations were most probably related to tidal cycling near the sampling site of fine grained particles from the MTZ located downstream. Significant differences in the behavior of the dissolved target oxyanions, mostly present in the <0.02μm fraction, occurred. The behavior of Sb was conservative. Variations of the dissolved As and V concentrations showed similar cycling trends, strongly related to tidal cycles. These As and V cycles were interpreted as a mixing between upstream freshwater and downstream water enriched in dissolved As and V by desorption from the MTZ particles. The observed trend in the variation of the dissolved Mo was more complex than that of As and Sb and attributed to the mixing of the water bodies mentioned above coupled to a point source input of dissolved Mo from an intra-estuarine source. The contribution of this suspected Mo source to the dissolved Mo concentrations measured at the sampling site was estimated from the ratio of dissolved Mo to dissolved As concentrations. The additional dissolved Mo signal, coupled to the monitored ebb and flood length and associated current velocities, suggested an anthropogenic input which may derive from industrial activity near the city of Bordeaux. Extrapolating these results to the annual scale suggested that this dissolved Mo may be equivalent to 45-90% of the annual dissolved Mo flux into the Garonne Branch, highlighting the importance to further investigate the origin and behavior of Mo in the fluvial estuary near Bordeaux.
机译:本工作报告了吉伦特河口(法国西南部)表层淡水河段中Sb,As,V和Mo浓度的时间变化。在波尔多市上游的固定站点连续两次涨潮期间,以高时间分辨率(每30分钟)采集的样品中测量了溶解的(<0.2和<0.02μm)和微粒Sb,As,V和Mo的浓度,最大值浊度区(MTZ)。另外,悬浮颗粒物浓度,理化参数,Cl-浓度,水深,流速和Th颗粒物浓度的测量是同时或连续进行的。获得的数据表明,As,V和Mo微粒浓度的变化很可能与来自下游MTZ的细颗粒采样点附近的潮汐循环有关。溶解的目标氧阴离子的行为存在显着差异,主要存在于<0.02μm的馏分中。 Sb的行为是保守的。溶解态砷和钒浓度的变化表现出相似的循环趋势,与潮汐循环密切相关。这些As和V循环被解释为上游淡水与通过从MTZ颗粒中解吸而富含溶解的As和V的下游水之间的混合。观察到的溶解态Mo变化趋势比As和Sb更为复杂,这归因于上述水体的混合,再加上河口内溶解态Mo的点源输入。根据溶解态钼与溶解态砷浓度之比,估算了这种可疑的钼源对在采样点测得的溶解态钼浓度的贡献。额外的溶解态Mo信号,加上监测到的潮起潮落和洪水时长以及相关的流速,表明人为输入可能来自波尔多市附近的工业活动。将这些结果推算到年尺度,表明这种溶解的Mo可能相当于每年流入Garonne分公司的Mo溶解量的45-90%,突出了进一步研究Mo在波尔多附近河口的起源和行为的重要性。

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