Department of Chemistry, Quaid-i-Azam University, Islamabad 45320, Pakistan.
Environ Monit Assess. 2012 Mar;184(3):1243-52. doi: 10.1007/s10661-011-2036-4. Epub 2011 Apr 6.
Selected trace metals were estimated by atomic absorption spectrometry in the water and soil samples collected from the remote region of Himalaya. The soil samples were analysed for soluble and acid extractable fraction of trace metals. In water samples, Ca, Na, Mg and K emerged as dominant contributors, whereas, Ca, Na, K, Mg, Fe and Pb were estimated at comparatively higher levels in the water extract of the soil. In case of acid extract of the soil samples, Ca, K, Fe, Mg, Mn and Na were found at elevated concentrations. Based on mean levels of the metals, following decreasing concentration order was observed in water samples: Ca > Na > Mg > K > Pb > Co > Cu > Zn > Mn > Cr > Fe > Cd > Li, however, in the acid extract of the soil, following order was noted: Ca > K > Fe > Mg > Mn > Na > Pb > Zn > Cr > Li > Cu > Co > Cd. The correlation study revealed appreciably diverse mutual relationships of trace metals in the water and soil samples. The multivariate cluster analyses exhibited divergent apportionment of trace metals in water and soil samples. Among the trace metals, Cd, Pb, Li, Zn, Cr, Cu, Mn and Co exhibited extreme to significant anthropogenic enrichment in the soil samples, while the rest of the metals were mostly contributed by the natural processes.
在喜马拉雅偏远地区采集的水和土壤样本中,通过原子吸收光谱法估计了选定的痕量金属。对土壤样本进行了痕量金属的可溶部分和酸可提取部分的分析。在水样中,Ca、Na、Mg 和 K 是主要的贡献者,而 Ca、Na、K、Mg、Fe 和 Pb 在土壤的水提取物中被估计为相对较高的水平。在土壤样本的酸提取物中,Ca、K、Fe、Mg、Mn 和 Na 的浓度较高。基于金属的平均水平,在水样中观察到以下浓度递减顺序:Ca > Na > Mg > K > Pb > Co > Cu > Zn > Mn > Cr > Fe > Cd > Li,然而,在土壤的酸提取物中,观察到以下顺序:Ca > K > Fe > Mg > Mn > Na > Pb > Zn > Cr > Li > Cu > Co > Cd。相关性研究揭示了水和土壤样本中痕量金属之间相当多样化的相互关系。多元聚类分析显示水和土壤样本中痕量金属的分配存在差异。在痕量金属中,Cd、Pb、Li、Zn、Cr、Cu、Mn 和 Co 在土壤样本中表现出极端到显著的人为富集,而其余金属主要由自然过程贡献。