Hua Haifeng, Liu Mingxuan, Liu Cong-Qiang, Lang Yunchao, Xue Hao, Li Shiyong, La Wei, Han Xiaokun, Ding Hu
Institute of Surface-Earth System Science, School of Earth System Science, Tianjin University, Tianjin 300072, China.
Institute of Surface-Earth System Science, School of Earth System Science, Tianjin University, Tianjin 300072, China; Tianjin Key Laboratory of Earth Critical Zone Science and Sustainable Development in Bohai Rim, Tianjin University, Tianjin 300072, China; Critical Zone Observatory of Bohai Coastal Region, Tianjin University, Tianjin 300072, China.
Sci Total Environ. 2023 May 20;874:162509. doi: 10.1016/j.scitotenv.2023.162509. Epub 2023 Mar 2.
The environmental behavior of heavy metals in soil is significantly regulated by their binding with dissolved organic matter (DOM), which is affected by soil moisture contents. However, the mechanism of this interaction in soils with varying moisture is still not well understood. Using a combination of ultrafiltration, Cu(II) titration, and multispectral (ultraviolet-visible absorption, 3D fluorescence, Fourier transform infrared) analysis techniques, we studied the differences in the spectral characteristics and Cu(II) binding properties of soil dissolved organic matter (DOM) and its different molecular weight (MW) fractions with moisture gradients. We found that the abundance and spectral characters of soil DOM changed with increasing soil moisture, i.e., the increase in abundance while the decrease in aromaticity and humification index. The components of DOM, shown by Fluorescence region-integration (FRI) analysis, also changed, with an increase in the proportion of protein-like substances and a decrease of humic-like and fulvic-like substances. The overall Cu(II) binding potential of soil DOM diminished with increasing soil moisture, as indicated by the fluorescence parallel factor (PARAFAC) analysis. This is aligns with the changes in DOM composition, as the humic-like and fulvic-like fractions exhibited higher Cu(II) binding potential compared to the protein-like fractions. The low MW fraction of the MW-fractionated samples showed a stronger binding potential for Cu(II) compared to the high MW fraction. Finally, the active binding site of Cu(II) in DOM, as revealed by UV-difference spectroscopy and 2D-FTIR-COS analysis, decreased with increasing soil moisture, with the order of preferentially functional groups shifting from OH, NH, and CO to CN and CO. This study emphasizes the impact of moisture variations on the characteristics of DOM and its interaction with Cu(II), providing insight into the environmental fate of heavy metal contaminants in soil in areas with alternating land and water conditions.
土壤中重金属的环境行为受到其与溶解有机物(DOM)结合的显著影响,而这又受土壤含水量的影响。然而,在不同含水量土壤中这种相互作用的机制仍未得到充分理解。我们结合超滤、Cu(II)滴定和多光谱(紫外-可见吸收、三维荧光、傅里叶变换红外)分析技术,研究了土壤溶解有机物(DOM)及其不同分子量(MW)组分在不同水分梯度下的光谱特征和Cu(II)结合特性的差异。我们发现,土壤DOM的丰度和光谱特征随土壤含水量增加而变化,即丰度增加而芳香性和腐殖化指数降低。荧光区域积分(FRI)分析显示,DOM的组分也发生了变化,类蛋白物质的比例增加,而类腐殖质和类富里酸物质减少。荧光平行因子(PARAFAC)分析表明,土壤DOM与Cu(II)的总体结合潜力随土壤含水量增加而降低。这与DOM组成的变化一致,因为类腐殖质和类富里酸组分相比类蛋白组分表现出更高的Cu(II)结合潜力。分子量分级样品的低分子量组分比高分子量组分对Cu(II)表现出更强的结合潜力。最后,紫外差光谱和二维傅里叶变换红外相关光谱(2D-FTIR-COS)分析表明,DOM中Cu(II)的活性结合位点随土壤含水量增加而减少,优先官能团的顺序从OH、NH和CO转变为CN和CO。本研究强调了水分变化对DOM特性及其与Cu(II)相互作用的影响,为水陆交替地区土壤中重金属污染物的环境归宿提供了见解。