Applications of stable isotope ratio mass spectrometry in cattle dung carbon cycling studies.
Applications of stable isotope ratio mass spectrometry in cattle dung carbon cycling studies.
复制标题
稳定同位素比质谱在牛粪碳循环研究中的应用。
DOI:
10.1002/rcm.4332
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发表时间:
2010
期刊:
影响因子:
--
通讯作者:
Dungait JA
中科院分区:
文献类型:
--
作者:
Dungait JA
Understanding the fate of dung carbon (C) in soils is challenging due to the ubiquitous presence of the plant‐derived organic matter (OM), the source material from which both dung‐derived OM and soil organic matter (SOM) predominantly originate. A better understanding of the fate of specific components of this substantial source of OM, and thereby its contribution to C cycling in terrestrial ecosystems, can only be achieved through the use of labelled dung treatments. In this short review, we consider analytical approaches using bulk and compound‐specific stable carbon isotope analysis that have been utilised to explore the fate of dung‐derived C in soils. Bulk stable carbon isotope analyses are now used routinely to explore OM matter cycling in soils, and have shown that up to 20% of applied dung C may be incorporated into the surface soil horizons several weeks after application, with up to 8% remaining in the soil profile after one year. However, whole soilδ13C values represent the average of a wide range of organic components with varyingδ13C values and mean residence times in soils. Several stable13C isotope ratio mass spectrometric methods have been developed to qualify and quantify different fractions of OM in soils and other complex matrices. In particular, thermogravimetry‐differential scanning calorimetry‐isotope ratio mass spectrometry (TG‐DSC‐IRMS) and gas chromatography‐combustion‐IRMS (GC‐C‐IRMS) analyses have been applied to determine the incorporation and turnover of polymeric plant cell wall materials from C4dung into C3grassland soils using natural abundance13C isotope labelling. Both approaches showed that fluxes of C derived from polysaccharides, i.e. as cellulose or monosaccharide components, were more similar to the behaviour of bulk dung C in soil than lignin. However, lignin and its 4‐hydroxypropanoid monomers were unexpectedly dynamic in soil. These findings provide further evidence for emerging themes in biogeochemical investigations of soil OM dynamics that challenge perceived concepts of recalcitrance of C pools in soils, which may have profound implications for the assessment of the potential of agricultural soils to influence terrestrial C sinks. Copyright © 2010 John Wiley & Sons, Ltd.
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影响因子:
2.8
作者:
S. Brookman;D. Chadwick;A. Retter
通讯作者:
A. Retter
影响因子:
2.4
作者:
B. N. Macdiarmid;B. Watkin
通讯作者:
B. Watkin
DOI:
10.1002/rcm.2145
发表时间:
2005
期刊:
Rapid communications in mass spectrometry : RCM
影响因子:
--
作者:
E. Lopez‐Capel;R. Bol;D. Manning
通讯作者:
D. Manning
影响因子:
9.7
作者:
Bol, R;Amelung, W;Ostle, N
通讯作者:
Ostle, N
影响因子:
5
作者:
DENIRO, MJ;EPSTEIN, S
通讯作者:
EPSTEIN, S