Soil Chemistry Group, Institute of Biogeochemistry and Pollutant Dynamics, Department of Environmental Systems Science, ETH Zurich, Universitätstrasse 16, CHN, CH-8092 Zurich, Switzerland.
Eawag, Swiss Federal Institute of Aquatic Science and Technology, Überlandstrasse 133, CH-8600 Dübendorf, Switzerland.
Environ Sci Process Impacts. 2022 Oct 19;24(10):1867-1882. doi: 10.1039/d2em00290f.
Complex interactions between redox-driven element cycles in soils influence iron mineral transformation processes. The rates and pathways of iron mineral transformation processes have been studied intensely in model systems such as mixed suspensions, but transformation in complex heterogeneous porous media is not well understood. Here, mesh bags containing 0.5 g of ferrihydrite were incubated in five water-saturated paddy soils with contrasting microbial iron-reduction potential for up to twelve weeks. Using X-ray diffraction analysis, we show near-complete transformation of the ferrihydrite to lepidocrocite and goethite within six weeks in the soil with the highest iron(II) release, and slower transformation with higher ratios of goethite to lepidocrocite in soils with lower iron(II) release. In the least reduced soil, no mineral transformations were observed. In soils where ferrihydrite transformation occurred, the transformation rate was one to three orders of magnitude slower than transformation in comparable mixed-suspension studies. To interpret the spatial distribution of ferrihydrite and its transformation products, we developed a novel application of confocal micro-Raman spectroscopy in which we identified and mapped minerals on selected cross sections of mesh bag contents. After two weeks of flooded incubation, ferrihydrite was still abundant in the core of some mesh bags, and as a rim at the mineral-soil interface. The reacted outer core contained unevenly mixed ferrihydrite, goethite and lepidocrocite on the micrometre scale. The slower rate of transformation and uneven distribution of product minerals highlight the influence of biogeochemically complex matrices and diffusion processes on the transformation of minerals, and the importance of studying iron mineral transformation in environmental media.
土壤中氧化还原驱动元素循环的复杂相互作用影响铁矿物转化过程。铁矿物转化过程的速率和途径在混合悬浮液等模型系统中得到了深入研究,但在复杂的多相多孔介质中的转化尚不清楚。在这里,含有 0.5 克水铁矿的网袋在 5 种具有不同微生物铁还原潜力的水饱和稻田土壤中培养,培养时间长达 12 周。使用 X 射线衍射分析,我们表明在铁(II)释放量最高的土壤中,水铁矿在六周内几乎完全转化为纤铁矿和针铁矿,而在铁(II)释放量较低的土壤中,转化速度较慢,针铁矿与纤铁矿的比例较高。在还原度最低的土壤中,未观察到矿物转化。在发生水铁矿转化的土壤中,转化速率比可比混合悬浮液研究中的转化速率慢一到三个数量级。为了解释水铁矿及其转化产物的空间分布,我们开发了共聚焦微拉曼光谱的新应用,在该应用中,我们在网袋内容物的选定横截面中识别和绘制了矿物。在淹水培养两周后,一些网袋的核心仍含有大量的水铁矿,而在矿物-土壤界面处则形成了一个边缘。反应的核心外层含有不均匀混合的水铁矿、针铁矿和纤铁矿,其粒径在微米级。转化速度较慢和产物矿物的不均匀分布突出了生物地球化学复杂基质和扩散过程对矿物转化的影响,以及在环境介质中研究铁矿物转化的重要性。