Organo–organic interactions dominantly drive soil organic carbon accrual

软土 土壤碳 Ultisol公司 土壤水分 有机质 环境化学 土壤有机质 化学 总有机碳 矿物 固碳 土壤科学 环境科学 有机化学 二氧化碳
作者
Jie Kang,Chenchen Qu,Wenli Chen,Peng Cai,Chengrong Chen,Qiaoyun Huang
出处
期刊:Global Change Biology [Wiley]
卷期号:30 (1) 被引量:17
标识
DOI:10.1111/gcb.17147
摘要

Abstract Organo–mineral interactions have been regarded as the primary mechanism for the stabilization of soil organic carbon (SOC) over decadal to millennial timescales, and the capacity for soil carbon (C) storage has commonly been assessed based on soil mineralogical attributes, particularly mineral surface availability. However, it remains contentious whether soil C sequestration is exclusively governed by mineral vacancies, making it challenging to accurately predict SOC dynamics. Here, through a 400‐day incubation experiment using 13 C‐labeled organic materials in two contrasting soils (i.e., Mollisol and Ultisol), we show that despite the unsaturation of mineral surfaces in both soils, the newly incorporated C predominantly adheres to “dirty” mineral surfaces coated with native organic matter (OM), demonstrating the crucial role of organo–organic interactions in exogenous C sequestration. Such interactions lead to multilayered C accumulation that is not constrained by mineral vacancies, a process distinct from direct organo–mineral contacts. The coverage of native OM by new C, representing the degree of organo–organic interactions, is noticeably larger in Ultisol (~14.2%) than in Mollisol (~5.8%), amounting to the net retention of exogenous C in Ultisol by 0.2–1.3 g kg −1 and in Mollisol by 0.1–1.0 g kg −1 . Additionally, organo–organic interactions are primarily mediated by polysaccharide‐rich microbial necromass. Further evidence indicates that iron oxides can selectively preserve polysaccharide compounds, thereby promoting the organo–organic interactions. Overall, our findings provide direct empirical evidence for an overlooked but critically important pathway of C accumulation, challenging the prevailing “C saturation” concept that emphasizes the overriding role of mineral vacancies. It is estimated that, through organo–organic interactions, global Mollisols and Ultisols might sequester ~0.1–1.0 and ~0.3–1.7 Pg C per year, respectively, corresponding to the neutralization of ca. 0.5%–3.0% of soil C emissions or 5%–30% of fossil fuel combustion globally.
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