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Lead Sequestration and Species Redistribution During Soil Organic Matter Decomposition

机译:土壤有机质分解过程中的铅固存和物种再分布

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The turnover of soil organic matter (SOM) maintains a dynamic chemical environment in the forest floor that can impact metal speciation on relatively short timescales. Here we measure the speciation of Pb in controlled and natural organic (O) soil horizons to quantify changes in metal partitioning during SOM decomposition in different forest litters. We provide a link between the sequestration of pollutant Pb in O-horizons, estimated by forest floor Pb inventories, and speciation using synchrotron-based X-ray fluorescence and X-ray absorption spectroscopy. When Pb was introduced to fresh forest O_i samples, it adsorbed primarily to SOM surfaces, but as decomposition progressed over two years in controlled experiments, up to 60% of the Pb was redistributed to pedogenic birnessite and ferrihydrite surfaces. In addition, a significant fraction of pollutant Pb in natural soil profiles was associated with similar mineral phases (~20-35%) and SOM (~65-80%). Conifer forests have at least 2-fold higher Pb burdens in the forest floor relative to deciduous forests due to more efficient atmospheric scavenging and slower organic matter turnover. We demonstrate that pedogenic minerals play an important role in surface soil Pb sequestration, particularly in deciduous forests, and should be considered in any assessment of pollutant Pb mobility.
机译:土壤有机质(SOM)的周转在林地中维持着动态的化学环境,这可以在相对较短的时间内影响金属形态。在这里,我们测量受控有机土壤和天然有机土壤中铅的形态,以量化不同森林凋落物中SOM分解过程中金属分配的变化。我们提供了通过森林地表铅的清单估算将O地平线中的污染物Pb隔离与使用基于同步加速器的X射线荧光和X射线吸收光谱的物种形成之间的联系。当将Pb引入新鲜森林O_i样品中时,它主要吸附在SOM表面,但是随着在受控实验中的分解历时两年,高达60%的Pb被重新分配到成岩水钠锰矿和水铁矿表面。此外,自然土壤剖面中的污染物Pb的很大一部分与相似的矿物相(约20-35%)和SOM(约65-80%)有关。针叶林的林地中铅含量比落叶林高出至少2倍,这是由于更有效的大气清除和较慢的有机质转换所致。我们证明,成岩矿物在表层土壤铅的螯合中,尤其是在落叶林中,起着重要的作用,并且在评估污染物铅的迁移性时都应考虑到这一点。

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