Stabilization of soil organic matter isolated via oxidative degradation

被引:164
作者
Eusterhues, K [1 ]
Rumpel, C
Kögel-Knabner, I
机构
[1] Tech Univ Munich, Lehrstuhl Bodenkunde, Wissenschaftszentrum Weihenstephan Ernahrung Land, D-85350 Freising Weihenstephan, Germany
[2] CNRS, Lab Biogeochem Milieux Continentaux, INRA, Ctr Versailles Grignon, F-78820 Thiverval Grignon, France
关键词
D O I
10.1016/j.orggeochem.2005.06.010
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Formation of long residence time carbon pools in soils is crucial for understanding the global carbon cycle. Acting on the assumption that chemical oxidation mimics natural oxidative processes, we treated forest floor, topsoil and subsoil samples from two acid forest soil profiles (Dystric Cambisol, Haplic Podzol) with H2O2. The oxidation-resistant organic carbon fraction was dated using C-14 and found to be 500 - 3900 years older than the bulk soil material. A positive correlation between the oxidation-resistant organic carbon and the amount of total iron oxides (dithionite-extractable Fe) exists for the subsoil samples of the Dystric Cambisol. In subsoils of the Haplic Podzol total iron oxides and the clay content are correlated with the oxidation-resistant organic carbon. This suggests that stabilization of the oxidation-resistant, old carbon fraction is caused by its interaction with iron oxides and/or other clay minerals rather than by chemical recalcitrance. In contrast to the subsoil, the topsoil samples have much higher concentrations of residual carbon relative to their iron oxide contents. Like forest floor horizons they probably contain additional, nonmineral-protected, but chemically recalcitrant, aliphatic organic matter, which is resistant to H2O2 treatment. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1567 / 1575
页数:9
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