School of Water and Environment, Chang'an University, No. 126 Yanta Road, Xi'an 710054, Shaanxi, China; Key Laboratory of Subsurface Hydrology and Ecological Effects in Arid Region of the Ministry of Education, Chang'an University, No. 126 Yanta Road, Xi'an 710054, Shaanxi, China; Key Laboratory of Eco-hydrology and Water Security in Arid and Semi-arid Regions of the Ministry of Water Resources, Chang'an University, No. 126 Yanta Road, Xi'an 710054, Shaanxi, China.
School of Water and Environment, Chang'an University, No. 126 Yanta Road, Xi'an 710054, Shaanxi, China; Key Laboratory of Subsurface Hydrology and Ecological Effects in Arid Region of the Ministry of Education, Chang'an University, No. 126 Yanta Road, Xi'an 710054, Shaanxi, China; Key Laboratory of Eco-hydrology and Water Security in Arid and Semi-arid Regions of the Ministry of Water Resources, Chang'an University, No. 126 Yanta Road, Xi'an 710054, Shaanxi, China.
Sci Total Environ. 2024 Aug 20;939:173506. doi: 10.1016/j.scitotenv.2024.173506. Epub 2024 May 28.
High levels of Iron (Fe) and manganese (Mn) in soils may contribute to secondary contamination of groundwater. However, there is limited understanding of the cycling mechanisms of Fe and Mn in groundwater and soil. This study aimed to investigate the biogeochemical processes constituting the Fe and Mn cycle by combining hydrochemistry, sequential extraction and microbiological techniques. The results indicated a similar vertical distribution pattern of Fe and Mn, with lower levels of the effective form (EFC-Fe/Mn) observed at the oxygenated surface, increasing near the groundwater table and decreasing below it. Generally, there was a tendency for accumulation above the water table, with Mn exhibiting a higher release potential compared to Fe. Iron‑manganese oxides (Ox-Fe/Mn) dominated the effective forms, with Fe and Mn in the soil entering groundwater through the reduction dissolution of Ox-Fe/Mn and the oxidative degradation of organic matter or sulfide (OM-Fe/Mn). Correlation analysis revealed that Fe and Mn tend to accumulate in media with fine particles and high organic carbon (TOC) contents. 16S rRNA sequencing analysis disclosed significant variation in the abundance of microorganisms associated with Fe and Mn transformations among unsaturated zone soils, saturated zone media and groundwater, with Fe/Mn content exerting an influence on microbial communities. Furthermore, functional bacterial identification results from the FAPROTAX database show a higher abundance of iron-oxidizing bacteria (9.3 %) in groundwater, while iron and manganese-reducing bacteria are scarce in both groundwater and soil environments. Finally, a conceptual model of Fe and Mn cycling was constructed, elucidating the biogeochemical processes in groundwater and soil environments. This study provides a new perspective for a deeper understanding of the environmental fate of Fe and Mn, which is crucial for mitigating Fe and Mn pollution in groundwater.
土壤中高浓度的铁(Fe)和锰(Mn)可能导致地下水的次生污染。然而,人们对地下水和土壤中 Fe 和 Mn 的循环机制知之甚少。本研究旨在通过结合水化学、连续提取和微生物学技术,研究构成 Fe 和 Mn 循环的生物地球化学过程。结果表明,Fe 和 Mn 具有相似的垂直分布模式,在充氧表面观察到较低的有效形态(EFC-Fe/Mn),在地下水面附近增加,在其下方减少。一般来说,在地下水面上方有积累的趋势,Mn 的释放潜力高于 Fe。铁锰氧化物(Ox-Fe/Mn)主导有效形态,土壤中的 Fe 和 Mn 通过 Ox-Fe/Mn 的还原溶解以及有机物或硫化物(OM-Fe/Mn)的氧化降解进入地下水。相关分析表明,Fe 和 Mn 倾向于在细颗粒和高有机碳(TOC)含量的介质中积累。16S rRNA 测序分析显示,不饱和带土壤、饱和带介质和地下水中与 Fe 和 Mn 转化相关的微生物丰度存在显著差异,Fe/Mn 含量对微生物群落有影响。此外,来自 FAPROTAX 数据库的功能细菌鉴定结果表明,地下水中铁氧化菌(9.3%)的丰度较高,而铁和锰还原菌在地下水中和土壤环境中都很稀缺。最后,构建了 Fe 和 Mn 循环的概念模型,阐明了地下水和土壤环境中的生物地球化学过程。本研究为深入了解 Fe 和 Mn 的环境归宿提供了新的视角,这对于减轻地下水的 Fe 和 Mn 污染至关重要。