Key Laboratory of Soil Environment and Pollution Remediation, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, 210008, China.
Key Laboratory of Soil Resources & Biotech Applications, Northwestern Bio-Agriculture Research Center, Chinese Academy of Sciences, Xi'an, 710043, China.
Environ Sci Pollut Res Int. 2018 Apr;25(11):11011-11022. doi: 10.1007/s11356-018-1405-8. Epub 2018 Feb 5.
Soil pollution by heavy metals (HMs) has rapidly become a major threat to vegetable security. Nearly all cultivated soils are at risk of metal accumulation, and greenhouse soils are among the most heavily impacted soils. In this study, a rapid assessment of HMs at trace concentrations was conducted via portable X-ray fluorescence (PXRF) spectroscopy in Shouguang, China. Measurements were made via PXRF under in situ, ex situ and sieved conditions and by inductively coupled plasma mass spectrometry (ICP-MS) after acid digestion. The performance of each PXRF measure relative to the ICP-MS method was assessed by linear regression. Redundancy analysis was performed to quantify the proportion of explained variability between the PXRF and ICP-MS data. Evaluation of the possible sources of HMs and their potential risks was then conducted by multivariate analysis. The results showed that the PXRF data were closely correlated with ICP-MS quantification for Cu, Mn and Zn, whereas no significant correlations were found for As, Ni and Pb. The uncertainties of PXRF measurement derived from soil heterogeneity accounted for 20.02% of total variability and those from moisture and particle size accounted for 20.15%. The geo-accumulation index (I) indicated that the greenhouse soils were potentially contaminated by Cu and Zn (I > 0), which can be attributed to anthropogenic activities. Overall, PXRF spectroscopy is promising as a rapid and nondestructive in situ technique for assessing the potential risks of HMs at trace concentrations in greenhouse soils.
土壤重金属污染(HMs)已迅速成为蔬菜安全的主要威胁。几乎所有耕地都有金属积累的风险,而温室土壤是受影响最严重的土壤之一。本研究在中国寿光通过便携式 X 射线荧光(PXRF)光谱法对痕量浓度的重金属进行了快速评估。通过 PXRF 在原位、异位和筛分条件下进行测量,并通过酸消解后用电感耦合等离子体质谱法(ICP-MS)进行测量。通过线性回归评估每种 PXRF 测量相对于 ICP-MS 方法的性能。通过冗余分析量化 PXRF 和 ICP-MS 数据之间的可解释变异比例。然后通过多元分析评估 HMs 的可能来源及其潜在风险。结果表明,对于 Cu、Mn 和 Zn,PXRF 数据与 ICP-MS 定量结果密切相关,而对于 As、Ni 和 Pb,则没有发现显著相关性。土壤异质性引起的 PXRF 测量不确定性占总变异性的 20.02%,水分和粒径引起的不确定性占 20.15%。地积累指数(I)表明,温室土壤可能受到 Cu 和 Zn 的污染(I>0),这归因于人为活动。总的来说,PXRF 光谱法有望成为一种快速、非破坏性的原位技术,用于评估温室土壤中痕量浓度重金属的潜在风险。