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受垃圾渗滤液影响的地下水中的生物衰减作用用 δ13C 进行追踪。

Bioattenuation in groundwater impacted by landfill leachate traced with δ13C.

机构信息

Groundwater Research Center, Faculty of Science, Ferdowsi University of Mashhad, PO Box 91775-1436, Mashhad, Iran.

出版信息

Ground Water. 2011 Nov-Dec;49(6):880-90. doi: 10.1111/j.1745-6584.2010.00790.x. Epub 2011 Feb 9.

DOI:10.1111/j.1745-6584.2010.00790.x
PMID:21306357
Abstract

The impact on groundwater imparted by the infiltration of high dissolved organic carbon (DOC) leachate from capped, unlined landfills can be attenuated by biogeochemical reactions beyond the waste source, although such reactive loss in the aquifer is difficult to distinguish from conservative advective dispersion. Compound-specific measurement of δ(13)C in carbon species, including CH(4), dissolved inorganic carbon (DIC), and the major DOC compounds (acetate, humic acid, and fulvic acid) provides a constraint in this assessment that can assist in exercises of modeling and prediction of leachate transport. The Trail Road municipal landfill near Ottawa, Ontario, Canada, hosts an unlined sector which produces a highly enriched leachate (DOC >4500 mg/L) that provides a good site to examine reactive attenuation within the receptor aquifer. Acetate, a sentinel component of leachate DOC (1000 mg C/L), is absent in impacted groundwater. Mass balance calculations together with reaction modeling suggest continued acetate fermentation with calcite control on DIC and δ(13)C(DIC) evolution. In groundwater within 50 m of the landfill, methane concentrations are elevated (10 mg/L), consistent with acetate fermentation, whereas δ(13)C(CH4) measurements in deeper groundwater range down to -51‰ compared with -60‰ in the landfill demonstrating oxidative loss. DOC in the deep aquifer is remarkably depleted to values less than -40‰ suggesting methanotrophic bacteria selectively consume isotopically light CH(4) to fix carbon. Continued reaction of leachate DOC in groundwater is demonstrated by evolution away from conservative mixing lines on diagrams of δ(13)C vs. concentrations of DIC and DOC.

摘要

受覆层未衬砌垃圾填埋场高溶解性有机碳(DOC)渗滤液影响的地下水,可以通过源区以外的生物地球化学反应得到缓解,尽管含水层中这种反应性的损失很难与保守的对流弥散区分开来。碳物种(包括 CH4、溶解无机碳(DIC)和主要的 DOC 化合物(乙酸盐、腐殖酸和富里酸)的 δ(13)C 的特定化合物测量,为评估提供了限制,有助于对渗滤液运移进行建模和预测。加拿大安大略省渥太华附近的 Trail Road 市政垃圾填埋场有一个未衬砌的区域,产生了高度浓缩的渗滤液(DOC>4500mg/L),这是一个很好的地点,可以在受体含水层内检查反应性衰减。乙酸盐是渗滤液 DOC 的一个示踪成分(约 1000mgC/L),在受影响的地下水中不存在。质量平衡计算和反应模型表明,随着方解石对 DIC 和 δ(13)C(DIC)演化的控制,乙酸盐继续发酵。在距离垃圾填埋场 50m 以内的地下水中,甲烷浓度升高(约 10mg/L),与乙酸盐发酵一致,而在更深的地下水中的 δ(13)C(CH4)测量值低至-51‰,而垃圾填埋场中的值为-60‰,表明发生了氧化损失。深部含水层中的 DOC 显著耗尽,值小于-40‰,这表明甲烷营养细菌选择性地消耗同位素较轻的 CH4 来固定碳。在 δ(13)C 与 DIC 和 DOC 浓度图上,远离保守混合线的演化表明,地下水继续反应渗滤液 DOC。

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