Division of Agricultural and Environmental Sciences, School of Biosciences, University of Nottingham, Sutton Bonington, Leicestershire LE12 5RD, UK.
Division of Soil and Water Sciences, Faculty of Environmental Agricultural Sciences, Suez Canal University, North Sinai 45516, Egypt.
Sci Total Environ. 2015 Jun 15;518-519:310-9. doi: 10.1016/j.scitotenv.2015.03.016. Epub 2015 Mar 12.
The solubility, lability and fractionation of zinc in a range of calcareous soils from Peshawar, Pakistan were studied (18 topsoils and 18 subsoils). The lability (E-value) of Zn was assessed as the fraction isotopically exchangeable with (70)Zn(2+); comparative extractions included 0.005 M DTPA, 0.43 M HNO3 and a Tessier-style sequential extraction procedure (SEP). Because of the extremely low concentration of labile Zn the E-value was determined in soils suspended in 0.0001 M Na2-EDTA which provided reliable analytical conditions in which approximately 20% of the labile Zn was dissolved. On average, only 2.4% of soil Zn was isotopically exchangeable. This corresponded closely to Zn solubilised by extraction with 0.005 DTPA and by the carbonate extraction step (F1+F2) of the Tessier-style SEP. Crucially, although the majority of the soil CaCO3 was dissolved in F2 of the SEP, the DTPA dissolved only a very small proportion of the soil CaCO3. This suggests a superficial carbonate-bound form of labile Zn, accessible to extraction with DTPA and to isotopic exchange. Zinc solubility from soil suspended in 0.01 M Ca(NO3)2 (PCO2 controlled at 0.03) was measured over three days. Following solution speciation using WHAM(VII) two simple solubility models were parameterised: a pH dependent 'adsorption' model based on the labile (isotopically exchangeable) Zn distribution coefficient (Kd) and an apparent solubility product (Ks) for ZnCO3. The distribution coefficient showed no pH-dependence and the solubility model provided the best fit to the free ion activity (Zn(2+)) data, although the apparent value of log10 Ks (5.1) was 2.8 log units lower than that of the mineral smithsonite (ZnCO3).
本研究测定了巴基斯坦白沙瓦地区一系列钙质土壤(18 个表土层和 18 个底土层)中锌的溶解性、活性和分馏作用。通过(70)Zn(2+)与土壤中可交换态锌(同位素交换可测锌)的比值评估 Zn 的活性(E 值)。对比提取方法包括 0.005 M DTPA、0.43 M HNO3 和 Tessier 连续提取程序(SEP)。由于可交换态 Zn 浓度极低,E 值是在 0.0001 M Na2-EDTA 悬浮土壤中测定的,该方法能提供可靠的分析条件,可溶解约 20%的可交换态 Zn。平均而言,只有 2.4%的土壤 Zn 具有同位素交换活性,与 0.005 DTPA 提取和 Tessier 连续提取程序碳酸盐提取步骤(F1+F2)溶解的 Zn 含量接近。重要的是,尽管 SEP 的 F2 中溶解了大部分土壤碳酸钙,但 DTPA 仅溶解了非常少量的土壤碳酸钙。这表明可交换态 Zn 存在于碳酸钙的表面结合形式,可通过 DTPA 提取和同位素交换来测定。将土壤悬浮于 0.01 M Ca(NO3)2(PCO2 控制在 0.03)中,3 天内测定土壤 Zn 溶解度。使用 WHAM(VII)进行溶液形态分析后,用两个简单的溶解度模型对参数进行了拟合:一个是基于可交换态 Zn 分配系数(Kd)和 ZnCO3 表观溶度积(Ks)的 pH 依赖型“吸附”模型;另一个是 pH 不依赖型模型。分配系数与 pH 无关,溶解度模型与自由离子活度(Zn(2+))数据拟合度最好,尽管表观 log10 Ks 值(5.1)比矿物菱锌矿(ZnCO3)低 2.8 个对数单位。