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铁在氧化还原界面上捕获陆源溶解有机质。

Iron traps terrestrially derived dissolved organic matter at redox interfaces.

机构信息

Institut für Geoökologie, Technische Universität Braunschweig, 38106 Braunschweig, Germany.

出版信息

Proc Natl Acad Sci U S A. 2013 Jun 18;110(25):10101-5. doi: 10.1073/pnas.1221487110. Epub 2013 Jun 3.

Abstract

Reactive iron and organic carbon are intimately associated in soils and sediments. However, to date, the organic compounds involved are uncharacterized on the molecular level. At redox interfaces in peatlands, where the biogeochemical cycles of iron and dissolved organic matter (DOM) are coupled, this issue can readily be studied. We found that precipitation of iron hydroxides at the oxic surface layer of two rewetted fens removed a large fraction of DOM via coagulation. On aeration of anoxic fen pore waters, >90% of dissolved iron and 27 ± 7% (mean ± SD) of dissolved organic carbon were rapidly (within 24 h) removed. Using ultra-high-resolution MS, we show that vascular plant-derived aromatic and pyrogenic compounds were preferentially retained, whereas the majority of carboxyl-rich aliphatic acids remained in solution. We propose that redox interfaces, which are ubiquitous in marine and terrestrial settings, are selective yet intermediate barriers that limit the flux of land-derived DOM to oceanic waters.

摘要

在土壤和沉积物中,活性铁和有机碳密切相关。然而,迄今为止,在分子水平上还没有对涉及的有机化合物进行特征描述。在泥炭地的氧化还原界面,铁和溶解有机质(DOM)的生物地球化学循环相耦合,这个问题很容易研究。我们发现,在两个重新湿地的好氧表层中铁氢氧化物的沉淀通过凝聚作用去除了大量的 DOM。在对缺氧沼泽孔隙水进行充气时,超过 90%的溶解铁和 27 ± 7%(平均值 ± 标准差)的溶解有机碳在 24 小时内迅速(在 24 小时内)被去除。使用超高分辨率 MS,我们表明,源自维管植物的芳香族和热解化合物被优先保留,而大多数富含羧基的脂肪族酸仍留在溶液中。我们提出,在海洋和陆地环境中普遍存在的氧化还原界面是选择性但又处于中间的屏障,限制了陆地来源的 DOM 向海洋水的通量。

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