Institute of Agricultural Resources and Environment, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China; Key Laboratory of Plant Nutrition and Fertilizer in South Region, Ministry of Agriculture, Guangzhou 510640, China; Guangdong Key Laboratory of Nutrient Cycling and Farmland Conservation, Guangzhou 510640, China.
Institute of Agricultural Resources and Environment, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China; Key Laboratory of Plant Nutrition and Fertilizer in South Region, Ministry of Agriculture, Guangzhou 510640, China; Guangdong Key Laboratory of Nutrient Cycling and Farmland Conservation, Guangzhou 510640, China.
Sci Total Environ. 2023 Jan 10;855:158710. doi: 10.1016/j.scitotenv.2022.158710. Epub 2022 Sep 11.
Iron (Fe) oxides are widely recognized to prevent the degradation of organic matter (OM) in environments, thereby promoting the persistence of organic carbon (OC) in soils. Thus, discerning the association mechanisms of Fe oxides and OC interactions is key to effectively influencing the dynamics and extent of organic C cycling in soils. Previous studies have focused on i) quantifying Fe oxide-bound organic carbon (Fe-OC) in individual environments, ii) investigating the distribution and adsorption capacity of Fe-OC, and iii) assessing the redox cycling and transformation of Fe-OC. Furthermore, the widespread application of high-tech instrumentation and methods has greatly contributed to a better understanding of the mechanism of organic mineral assemblages in the past few decades. However, few literature reviews have comprehensively summarized Fe-OC distributions, associations, and characteristics in soil-plant systems. Here, studies investigating the Fe-OC contents among different environments are reviewed. In addition, the mechanisms and processes related to OM transformation dynamics occurring at mineral-organic interfaces are also described. Recent studies have highlighted that diverse interactions occur between Fe oxides and OC, with organic compounds adhering to Fe oxides due to their huge specific surfaces area and active reaction sites. Moreover, we also review methods for understanding Fe-OC interactions at micro-interfaces. Lastly, developmental prospects for understanding coupled Fe-OC geochemical processes in soil environments at molecular- and nano-scales are outlined. The summary suggests that combined advanced techniques and methods should be used in future research to explore micro-interfaces and in situ descriptions of organic mineral assemblages. This review also suggests that future studies need to consider the functional and spatial complexity that is typical of soil/sediment environments where Fe-OC interactions occur.
铁氧化物被广泛认为可以防止环境中有机物(OM)的降解,从而促进土壤中有机碳(OC)的持久性。因此,辨别铁氧化物和 OC 相互作用的关联机制是有效影响土壤中有机碳循环动态和程度的关键。以前的研究主要集中在 i)量化个体环境中铁氧化物结合的有机碳(Fe-OC),ii)研究 Fe-OC 的分布和吸附能力,以及 iii)评估 Fe-OC 的氧化还原循环和转化。此外,高科技仪器和方法的广泛应用极大地促进了过去几十年中对有机矿物组合机制的理解。然而,很少有文献综述全面总结了土壤-植物系统中 Fe-OC 的分布、关联和特征。在这里,我们综述了研究不同环境中 Fe-OC 含量的文献。此外,还描述了与矿物-有机界面上 OM 转化动力学相关的机制和过程。最近的研究强调,铁氧化物和 OC 之间存在多种相互作用,由于其巨大的比表面积和活跃的反应位点,有机化合物附着在铁氧化物上。此外,我们还综述了理解微界面中铁-OC 相互作用的方法。最后,概述了在分子和纳米尺度上理解土壤环境中耦合的 Fe-OC 地球化学过程的发展前景。综述表明,未来的研究应结合先进的技术和方法,以探索微界面和有机矿物组合的原位描述。该综述还表明,未来的研究需要考虑到 Fe-OC 相互作用发生的土壤/沉积物环境的功能和空间复杂性。