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首页> 外文期刊>Organic Geochemistry: A Publication of the International Association of Geochemistry and Cosmochemistry >Concentrations, sulfur isotopic compositions and origin of organosulfur compounds in pore waters of a highly polluted raised peatland
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Concentrations, sulfur isotopic compositions and origin of organosulfur compounds in pore waters of a highly polluted raised peatland

机译:高污染泥炭地孔隙水中的浓度,硫同位素组成和有机硫化合物的来源

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Sulfur cycling in peatlands plays a key role in their response to atmospheric deposition of acid sulfate: however, the role of dissolved organic sulfur species has received little attention. in this study, we assess the quantitative importance of dissolved organic sulfur species in a heavily polluted peatland and their role in sulfur cycling. Surface and pore waters from a raised peat bog have been analyzed for dissolved organic and inorganic species. Except in the surface water, organically bound sulfur dominates over sulfate sulfur and the organosulfur is predominantly in the humic fraction, which is not GC amenable. Two organosulfur compounds are present in the GC amenable fraction at all depths; a compound containing a benzene ring, sulfone and amide groups dominates while a compound closely similar to either benzothiazole or 1,2-benzisothiazole is present at 100-1000 times lower concentrations. Other organosulfur species were detected in some samples by GC-AED (gas chromatography-atomic emission detection) at similar or yet lower concentrations but not identifiable with GC-MS. In the shallowest parts of the peat, sulfur isotopic data on the humic and non-humic dissolved organic sulfur fractions show a pronounced difference, implying different sources for these organosulfur compounds. Humic organosulfur is S-34 enriched, indicating a source for this component from breakdown of plant materials, which have similar delta S-34 (0.1 parts per thousand and 4.2 parts per thousand). By contrast, the non-humic organosulfur is more S-34 depleted at shallow depths (-11.7 parts per thousand in surface water), indicating an origin from reaction of bacterially produced sulfide (-9.9 parts per thousand in surface water) with dissolved organic material. Deeper in the peat the non-humic organosulfur becomes more S-34 enriched (up to +6.8 parts per thousand), which may result from either: (i) reactions between organic material and more S-34 enriched sulfide; or (less likely) (ii) a shift to production of non-humic organosulfur by breakdown of humic compounds or plant material in the peat matrix. These data highlight the importance of organosulfur species relative to inorganic species in peatland groundwaters. Organosulfur species comprise the bulk of the dissolved sulfur budget and are involved in the bacterial cycling of sulfur in the peatland ecosystem.
机译:泥炭地中的硫循环在其对酸性硫酸盐在大气中的响应中起着关键作用:但是,溶解的有机硫物质的作用却很少受到关注。在这项研究中,我们评估了重污染泥炭地中溶解有机硫物种的定量重要性及其在硫循环中的作用。分析了来自凸起泥炭沼泽的地表水和孔隙水中溶解的有机和无机物质。除了在地表水中,有机结合的硫比硫酸硫占主导地位,有机硫主要在腐殖质馏分中,这是GC所不适合的。在所有深度的GC适宜馏分中均存在两种有机硫化合物;含有苯环,砜和酰胺基的化合物占主导地位,而与苯并噻唑或1,2-苯并噻唑相似的化合物则以低100-1000倍的浓度存在。通过GC-AED(气相色谱-原子发射检测)在某些样品中检测到其他有机硫物质,其浓度相似或更低,但GC-MS无法鉴定。在泥炭的最浅部分,腐殖质和非腐殖质溶解的有机硫馏分的硫同位素数据显示出明显的差异,这意味着这些有机硫化合物的来源不同。腐殖质中的有机硫富含S-34,表明该成分的来源来自植物材料的分解,这些植物具有类似的δ-S-34(0.1份/千份和4.2份/千份)。相比之下,非腐殖质有机硫在浅深度(地表水中每千分之一-11.7份)中消耗的S-34较多,表明细菌产生的硫化物(地表水中每千分之-9.9份)与溶解有机物的反应起源材料。在泥炭中更深处,非腐殖质有机硫变得更富S-34(最高至千分之6.8),这可能是由于以下原因之一:(i)有机物质与更富S-34的硫化物之间的反应; (ii)通过分解泥炭基质中的腐殖质化合物或植物原料而转向生产非腐殖质有机硫。这些数据突出了泥炭地地下水中有机硫物种相对于无机物种的重要性。有机硫物质占溶解硫预算的大部分,并参与泥炭地生态系统中硫的细菌循环。

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