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Sequestration of maize crop straw C in different soils: role of oxyhydrates in chemical binding and stabilization as recalcitrance 总被引:1,自引:0,他引:1
While biophysical controls on the sequestration capacity of soils have been well addressed with physical protection, chemical binding and stabilization processes as well as microbial community changes, the role of chemical binding and stabilization has not yet well characterized for soil organic carbon (SOC) sequestration in rice paddies. In this study, a 6-month laboratory incubation with and without maize straw amendment (MSA) was conducted using topsoil samples from soils with different clay mineralogy and free oxy-hydrate contents collected across Southern China. The increase in SOC under MSA was found coincident with that in Fe- and Al-bound OC (Fe/Al-OC) after incubation for 30 d (R(2)=0.90, P=0.05), and with sodium dithionate-citrate-bicarbonate (DCB) extractable Fe after incubation for 180 d (R(2)=0.99, P<0.01). The increase in SOC under MSA was found higher in soils rich in DCB extractable Fe than those poor in DCB extractable Fe. The greater SOC sequestration in soils rich in DCB extractable Fe was further supported by the higher abundance of (13)C which was a natural signature of MSA. Moreover, a weak positive correlation of the increased SOC under MSA with the increased humin (R(2)=0.87, P=0.06) observed after incubation for 180 d may indicate a chemical stabilization of sequestered SOC as humin in the long run. These results improved our understanding of SOC sequestration in China's rice paddies that involves an initial chemical binding of amended C and a final stabilization as recalcitrant C of humin. 相似文献
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Jufeng Zheng Xuhui Zhang Lianqing Li Pingjiu Zhang Genxing Pan 《Agriculture, ecosystems & environment》2007,120(2-4):129-138
Impacts of nutrient management on C mineralization and greenhouse gas (GHGs) emission from soils have been of much concern in global change. Using laboratory incubation, the production of CH4 and CO2 were studied from both bulk samples and the particle size fractions (PSF) of topsoil from a paddy under a long-term different fertilization trial (including non (NF), chemical without (CF) and with manure (CFM) fertilization, respectively) in the Tai Lake Region, China. Four PSFs (2000–200, 200–20, 20–2, <2 μm) were separated from undisturbed samples collected after rice harvest by a low-energy ultrasonic dispersion procedure. Both the bulk samples and PSFs were incubated under submerged condition for 72 days. The concentration of CH4 and CO2 evolved during incubation were determined by gas chromatography. C mineralization rates ranged from 0.13 to 0.52 mg C g−1 C day−1, with different fertilizations and size of the PSFs, and were not correlated with C/N ratio. While CO2 production predominated over CH4 from C mineralization from both bulk samples and the size fractions, CH4 production played a predominant role in the total global warming potential (GWP) under all treatments. C mineralization of bulk soil was significantly higher under CF than under CFM and NF. CH4 production, however, was 3 times as under CFM and 27 times as under NF, indicating a tremendous effect of chemical fertilization alone on the total GWP. CO2 production from the PSFs differed from CH4 under a single treatment, which was notably from the coarse PSFs larger than 200 μm. Higher C mineralization and CH4 production with a higher metabolic quotient under CF implicated a vulnerability of soil functioning of GHGs mitigation in the paddy receiving chemical fertilizers only. Thus, rational organic amendments should be undertaken for mitigating the climate change. 相似文献
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