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Corrigendum to “Seasonal variation in water uptake patterns of two greening species and their responses to rainfall events in a subtropical megacity of China” [J. Hydrol. (2023) 129262]

黄土 浸出(土壤学) 土壤水分 导水率 环境科学 溶解 地质学 土壤科学 环境化学 化学 地貌学 物理化学
作者
Bei Wang,Yan Chen,Zhe Shi,Jian Ding,Tengran Zhang,Lu Qin,Guo Yu Qiu
出处
期刊:Journal of Hydrology [Elsevier]
卷期号:620: 129462-129462
标识
DOI:10.1016/j.jhydrol.2023.129462
摘要

Heavy metal contamination in soils can pose severe challenges to the safety of geotechnical engineering projects. Loess, which is widely distributed in Northwest China, is a preferred engineering construction material for anti-fouling barriers. Therefore, research on the influence of heavy metal ions on its seepage performance is urgently required. To obtain new insights into the seepage behavior of heavy metal-contaminated loess and its underlying geochemical mechanism, laboratory investigations were performed on the saturated hydraulic conductivity (Ksat), leaching, and microstructural characteristics of loess contaminated with Cu2+ and Zn2+. The results indicate that the hydrolysis of Zn2+ creates an acidic environment, which promotes the dissolution of carbonate minerals in loess, enhances the leaching capacity, and leads to the quantitative transformation of small pores (2–8 μm) to mesopores (8–32 μm). Meanwhile, the alternating adsorption of Zn2+ and its diffuse double-layer effect compresses the diffusion layer, increasing the abundance of free water channels. Thus, the Ksat of Zn-contaminated loess increases by 81.2% during the seepage period. As for Cu-contaminated loess, its seepage behavior is the opposite of that of Zn-contaminated loess, with a Ksat decrease of nearly 50%. The primary factor controlling this phenomenon is the formation and enrichment of Cu2O in the lower part of the soil, which inhibits the enlargement of pores and reduces the effective connectivity of pores. The findings of this work provide insight into the seepage behavior of saturated loess under erosion by heavy metals and the underlying geochemical mechanism thereof.
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