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Distribution and Pools of Mercury in Czech Forest Soils

机译:捷克森林土壤中汞的分布和储量

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Parts of the Czech Republic received extreme loading of acid deposition from coal combustion in the second half of the twentieth century. Although associated Hg deposition was not directly measured, Hg deposition rates calculated from peat cores approach 100 ng m~(-2) year~(-1). We quantified the soil concentrations and pools of Hg with carbon (C), sulfur (S), and nitrogen (N)—elements closely associated with soil organic matter at five sites across the Czech Republic-four sites known for extreme deposition levels of S and N compounds in the twentieth century, and one site relatively less impacted. The site-specific means of O-horizon Hg concentrations ranged from 277 to 393μg kg~(-1), while means of Hg concentrations in mineral soil ranged from 22 to 95 μg kg~(-1). The mean Hg/C ratio across sites increased from ~0.5 μg Hg g~(-1) C in the Oi-horizon to ~5 μg Hg g~(-1)C in the C-horizon due to the progressive mineralization of soil organic matter. The soil Hg/C increase was accompanied by a soil C/N decrease, another indicator of soil organic matter mineralization. Soil Hg/C also increased as soil C/S decreased, suggesting that Hg was stabilized by S functional groups within the soil organic matter. Mineral soil Hg pools (8.9-130.0 mg m~(-2)) dominated over organic soil Hg pools (5.3-10.1 mg m~(-2)) at all sites. Mineral soil Hg pools correlated more strongly with total soil S and oxalate-extractable Fe than with total soil C. Total soil Hg pools could be accounted for by a time period of atmospheric inputs that was short relative to the age of the soils. The cross site variability of Hg soil pools was not sensitive to the local Hg deposition history but rather related to the capacity of soil to store and stabilize organic matter.
机译:在20世纪下半叶,捷克共和国的部分地区因煤炭燃烧而承受了极高的酸沉降量。尽管没有直接测量相关的汞沉积,但是根据泥炭芯计算出的汞沉积速率接近100 ng m〜(-2)年〜(-1)。我们用碳(C),硫(S)和氮(N)量化了土壤中汞的浓度和汞储量,这些元素与捷克共和国5个地点中的土壤有机质紧密相关-4个地点因S的极端沉积水平而闻名和20世纪的N化合物,并且其中一个地点受到的影响相对较小。特定水平的O水平水银Hg浓度范围为277至393μgkg〜(-1),而矿质土壤中Hg浓度的平均值范围为22至95μgkg〜(-1)。由于土壤逐渐矿化,跨站点的平均Hg / C比值从Oi地平线上的〜0.5μgHg g〜(-1)C增加到C地平线上的〜5μgHg g〜(-1)C有机物。土壤Hg / C的增加伴随着土壤C / N的降低,这是土壤有机质矿化的另一个指标。土壤Hg / C也随着土壤C / S的减少而增加,表明Hg被土壤有机质中的S官能团稳定。在所有地点,矿质土壤汞库(8.9-130.0 mg m〜(-2))高于有机土壤汞库(5.3-10.1 mg m〜(-2))。矿质土壤汞库与总土壤S和草酸盐可萃取铁的相关性比与总土壤C的相关性更强。大气汞输入的总时间可能是相对于土壤年龄较短的一段时间的大气输入造成的。汞土壤库的跨站点变异性对当地汞的沉积历史并不敏感,而与土壤存储和稳定有机质的能力有关。

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