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Mercury and methylmercury in the sediments of Lake St. Clair (Michigan, Ontario).

机译:圣克莱尔湖(安大略省密歇根州)沉积物中的汞和甲基汞。

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摘要

Lake St. Clair is a wide, shallow lake situated midway between Lake Huron and Lake Erie. The lake basin has been a region of significant mercury contamination for several decades due to intense industrial activities, largely those of chlor-alkali plants located up-river. As the lake flushes very rapidly (t R ∼ 4 days), little sedimentation takes place, hence it was expected that most contaminants would be carried downstream to Lake Erie. The persistence of Hg in the upper sediments and biota indicates that some other processes may be at work. Inorganic mercury that has been released to the environment can be converted through bacterial and photochemical pathways to methylmercury, which is highly toxic and is an efficient bioaccumulator. It was suspected that the delta of the inflowing St. Clair River has acted as a sink while the original discharge was taking place, and now, with its large areas of marshland and standing water, it may be converting this to methylmercury and releasing it to the ecosystem. In order to investigate this, sediment core samples were collected from various sites in the lake and the delta in the summer or 1997. Previous work in quantifying methylmercury in the environment has relied largely on methods which provide indirect confirmation of methylmercury (e.g. CV-AAS, GC-ECD). As a part of this study, a method was developed to overcome this limitation. In this method, methylmercury is isolated from the sediment matrix by solvent extraction and then derivatized to form a species more amenable to separation by gas chromatography. Element-specific detection was accomplished using a microwave plasma-atomic emission detector. Paper copy at Leddy Library: Theses u26 Major Papers - Basement, West Bldg. / Call Number: Thesis1999 .T66. Source: Masters Abstracts International, Volume: 39-02, page: 0508. Adviser: Brian J. Fryer. Thesis (M.Sc.)--University of Windsor (Canada), 1999.
机译:圣克莱尔湖是一个宽而浅的湖,位于休伦湖和伊利湖之间。由于激烈的工业活动,主要是位于上游的氯碱工厂的活动,该湖盆地几十年来一直是汞污染严重的地区。由于湖水冲刷非常快(t R〜4天),几乎没有沉淀,因此,预计大多数污染物将被带到伊利湖下游。汞在上部沉积物和生物区系中的持续存在表明其他一些过程可能还在起作用。释放到环境中的无机汞可以通过细菌和光化学途径转化为甲基汞,甲基汞的毒性很高,是一种有效的生物蓄积剂。有人怀疑流入的圣克莱尔河三角洲曾在最初的排放发生时充当汇,现在,由于沼泽地和死水面积很大,它可能会将其转化为甲基汞并将其释放到生态系统。为了对此进行调查,在夏季或1997年从湖泊和三角洲的不同地点收集了沉积物核心样品。量化环境中甲基汞的先前工作主要依赖于提供甲基汞间接确认的方法(例如CV-AAS)。 ,GC-ECD)。作为这项研究的一部分,开发了一种克服此限制的方法。在这种方法中,通过溶剂萃取从沉积物基质中分离出甲基汞,然后将其衍生化,形成更适合通过气相色谱法分离的物质。使用微波等离子体原子发射检测器可以完成元素特异性检测。莱迪图书馆的纸质副本:论文主要论文-西楼地下室。 /致电:Thesis1999 .T66。资料来源:国际硕士摘要,第39卷,第0508页。顾问:布莱恩·弗莱尔(Brian J. Fryer)。论文(硕士)-温莎大学(加拿大),1999。

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    Toms Andrew David.;

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