Molecular Evolution of Organic Matter Humification Governs Ferrihydrite Transformation: Interfacial Electron Transfer Mechanisms and Carbon Preservation Implications

IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL
环境科学与技术 Pub Date : 2026-06-16 Epub Date: 2026-06-03 DOI:10.1021/acs.est.5c15760
Wenfeng Huang, Bo Chen, Jingyi Zhang, Chengpeng Yuan, Zehong Zhang, Quan Qian, Kexin Chen, Qi Liu, Xiangyang Gui, Liyang Hu, Xinde Cao and Xiaoyun Xu*, 
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引用次数: 0

Abstract

During soil humification, organic matter (OM) develops distinct compositional and chemical signatures across the progressive stages. However, how these evolving OM characteristics influence iron (hydr)oxide transformation and ultimately regulate carbon preservation remains unclear. Through controlled anaerobic incubation experiments with ferrihydrite (Fh) and straw-derived OM from sequential soil humification stages under Fe(II)-mediated conditions, we found that advancing humification increasingly inhibited Fh crystallization, reducing its transformation to lepidocrocite/goethite from 45.3% in the degradation stage to 21.5% in the maturation stage. This stage-dependent inhibition correlated strongly with the accumulation of highly unsaturated and phenolic compounds (HUPs), which disrupted interfacial electron transfer and mineral nucleation, which are key processes in secondary mineral formation. Mechanistically, HUPs facilitated ternary Fh-OM-Fe(II) complex formation via the C–O–Fe bond, enhancing Fe(II) adsorption while narrowing the Fe(II)-Fh redox potential gap to suppress interfacial electron transfer. Furthermore, HUPs reduced the mineral surface potential and impeded particle agglomeration, thereby disrupting the crystallization of nucleation precursors. Consequently, the inhibited Fh transformation facilitated the selective adsorption of HUPs and their molecular conversion to condensed aromatics, thereby preferentially preserving organic carbon from advanced humification stages. These findings highlight the stage-dependent regulation of Fh transformation by humified OM and its implication for carbon preservation, advancing our understanding of coupled carbon–iron biogeochemistry in soils.

Abstract Image

有机质腐殖质化的分子演化控制着水合铁的转变:界面电子转移机制和碳保存意义。
在土壤腐殖质化过程中,有机质(OM)在各个阶段形成了不同的组成和化学特征。然而,这些变化的OM特性如何影响铁(氢)氧化物转化并最终调节碳保存仍不清楚。在Fe(II)调节条件下,通过对连续土壤腐殖质化阶段的水合铁(Fh)和秸秆来源的OM进行可控厌氧培养实验,我们发现,推进腐殖质化对Fh结晶的抑制作用日益增强,使其向蛭石/针铁矿的转化从降解阶段的45.3%降低到成熟阶段的21.5%。这种阶段依赖性抑制与高不饱和酚类化合物(HUPs)的积累密切相关,后者破坏了界面电子转移和矿物成核,而这是次生矿物形成的关键过程。从机理上看,HUPs通过C-O-Fe键促进了Fh-OM-Fe(II)三元配合物的形成,增强了Fe(II)的吸附,同时缩小了Fe(II)-Fh氧化还原电位间隙,抑制了界面电子转移。此外,HUPs降低了矿物表面电位,阻碍了颗粒团聚,从而破坏了成核前体的结晶。因此,抑制的Fh转化促进了HUPs的选择性吸附及其分子转化为缩合芳烃,从而优先保存了腐殖质化后期的有机碳。这些发现强调了腐殖化OM对Fh转化的阶段性调控及其对碳保存的意义,促进了我们对土壤碳-铁耦合生物地球化学的理解。
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来源期刊
环境科学与技术
环境科学与技术 环境科学-工程:环境
CiteScore
17.50
自引率
9.60%
发文量
12359
审稿时长
2.8 months
期刊介绍: Environmental Science & Technology (ES&T) is a co-sponsored academic and technical magazine by the Hubei Provincial Environmental Protection Bureau and the Hubei Provincial Academy of Environmental Sciences. Environmental Science & Technology (ES&T) holds the status of Chinese core journals, scientific papers source journals of China, Chinese Science Citation Database source journals, and Chinese Academic Journal Comprehensive Evaluation Database source journals. This publication focuses on the academic field of environmental protection, featuring articles related to environmental protection and technical advancements.
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