Soil Chemistry Group, Institute of Biogeochemistry and Pollutant Dynamics, CHN, ETH Zurich, Zurich 8092, Switzerland.
Department of Soil Science, Faculty of Agriculture, Kasetsart University, Bangkok 10900, Thailand.
Environ Sci Technol. 2024 Jun 18;58(24):10601-10610. doi: 10.1021/acs.est.4c01519. Epub 2024 Jun 4.
The mobility and bioavailability of phosphate in paddy soils are closely coupled to redox-driven Fe-mineral dynamics. However, the role of phosphate during Fe-mineral dissolution and transformations in soils remains unclear. Here, we investigated the transformations of ferrihydrite and lepidocrocite and the effects of phosphate pre-adsorbed to ferrihydrite during a 16-week field incubation in a flooded sandy rice paddy soil in Thailand. For the deployment of the synthetic Fe-minerals in the soil, the minerals were contained in mesh bags either in pure form or after mixing with soil material. In the latter case, the Fe-minerals were labeled with Fe to allow the tracing of minerals in the soil matrix with Fe Mössbauer spectroscopy. Porewater geochemical conditions were monitored, and changes in the Fe-mineral composition were analyzed using Fe Mössbauer spectroscopy and/or X-ray diffraction analysis. Reductive dissolution of ferrihydrite and lepidocrocite played a minor role in the pure mineral mesh bags, while in the Fe-mineral-soil mixes more than half of the minerals was dissolved. The pure ferrihydrite was transformed largely to goethite (82-85%), while ferrihydrite mixed with soil only resulted in 32% of all remaining Fe present as goethite after 16 weeks. In contrast, lepidocrocite was only transformed to 12% goethite when not mixed with soil, but 31% of all remaining Fe was found in goethite when it was mixed with soil. Adsorbed phosphate strongly hindered ferrihydrite transformation to other minerals, regardless of whether it was mixed with soil. Our results clearly demonstrate the influence of the complex soil matrix on Fe-mineral transformations in soils under field conditions and how phosphate can impact Fe oxyhydroxide dynamics under Fe reducing soil conditions.
在稻田土壤中,磷酸盐的迁移性和生物可利用性与氧化还原驱动的铁矿物动态密切相关。然而,在土壤中,磷酸盐在铁矿物溶解和转化过程中的作用仍不清楚。在这里,我们研究了针铁矿和纤铁矿的转化以及在泰国水淹沙质水稻田中进行的 16 周田间培养过程中,预吸附到针铁矿上的磷酸盐的作用。为了在土壤中部署合成铁矿物,这些矿物要么以纯形式,要么与土壤材料混合后装入网袋中。在后一种情况下,铁矿物用 Fe 标记,以便用 Fe Mössbauer 光谱法追踪土壤基质中的矿物。监测了孔隙水地球化学条件,并使用 Fe Mössbauer 光谱法和/或 X 射线衍射分析来分析铁矿物组成的变化。纯矿物网袋中的针铁矿和纤铁矿的还原溶解作用作用较小,而在铁矿物-土壤混合物中,超过一半的矿物溶解。纯针铁矿主要转化为针铁矿(82-85%),而针铁矿与土壤混合仅导致 16 周后所有剩余 Fe 中有 32%以针铁矿形式存在。相比之下,当未与土壤混合时,纤铁矿仅转化为 12%的针铁矿,但当与土壤混合时,所有剩余 Fe 中有 31%以针铁矿形式存在。吸附态的磷酸盐强烈阻碍了针铁矿向其他矿物的转化,无论是否与土壤混合。我们的研究结果清楚地表明了复杂的土壤基质对土壤中铁矿物在田间条件下转化的影响,以及磷酸盐如何在还原条件下影响铁氢氧化物动力学。