加纳西南部塔克瓦典型锰矿社区Nsuta居住土壤中潜在有毒元素的空间分布及来源解析

Eric Gyimah , Samuel Kwamena , Shadrack Fosu , Emmanuel Daanoba Sunkari , David Edem Dinku , Yao Yevenyo Ziggah
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摘要

城市社区居住区的环境质量受到快速工业增长、大量技术创新和城市扩张的威胁。本研究基于化学计量受体模型进行了塔尔克瓦矿区居住土壤中砷、镉、铅、汞、锰和铁的源解析、生态毒理学状况和空间分布。重金属分布呈广泛分布,研究区东部边缘为汞污染热点地区。聚类分析(CA)、主成分分析(PCA)和正矩阵分解(PMF)与相关矩阵(CM)的一致,合理地确定了Nsuta群落居住土壤中砷、锰和铁的污染来源受变质火山岩风化和水形态分散等地质因素的影响。值得注意的是,大气沉积被认为是汞污染的优先来源,PMF贡献了78.50%。车辆排放和其他人为活动对研究区内居住土壤的铅(48.00%)和镉(66.20%)污染有贡献。生态毒理学评估显示,综合毒性风险指数(TRI)为29.80,汞约占总风险的97.50%。此外,单一金属的修正危害商(mHQi)也表明汞(Hg)具有最高的生态毒性水平,其mHQi值为7.00。本研究提供的基线数据可能对适当的环境管理和决策有价值,以减少研究地区大量重金属污染的流入。为了全面了解Nsuta群落的金属污染,还需要进一步研究金属在土壤中的形态、生物利用度、生物积累、潜在的作用方式以及对人类健康的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spatial distribution and source apportionment of potentially toxic elements in residential soil from Nsuta, a typical manganese mine community in Tarkwa, Southwestern Ghana

Spatial distribution and source apportionment of potentially toxic elements in residential soil from Nsuta, a typical manganese mine community in Tarkwa, Southwestern Ghana
The environmental quality of residential areas of urban communities has been threatened by rapid industrial growth, substantial technological innovation, and urban expansion. The present study provides chemometric receptor model-based source apportionment, the ecotoxicological status, and the spatial distribution of arsenic, cadmium, lead, mercury, manganese and iron in residential soils in a mining community in Tarkwa. The distributions of the heavy metals showed a widespread pattern, while the eastern fringe of the study area was identified as a hotspot for mercury contamination. Agreement among the cluster analysis (CA), principal component analysis (PCA), and positive matrix factorization (PMF) along with the correlation matrix (CM) reasonably identified the sources of arsenic, manganese, and iron contamination of residential soils of the Nsuta community to be governed by geogenic influences such as the weathering and hydromorphic dispersion from the metavolcanic rocks. Noteworthily, atmospheric deposition is considered a prioritized source for mercury contamination, with a PMF contribution of 78.50%. Vehicular emission as well as other anthropogenic activities contribute to lead (48.00%) and cadmium (66.20%) contamination of the residential soil within the study area. Ecotoxicological assessment reveals a combined toxic risk index (TRI) of 29.80, with mercury contributing to about 97.50% of the total risk. Moreover, the modified hazard quotient (mHQi) for the single metals also indicated that mercury (Hg) has the highest ecological toxicity level with a mHQi value of 7.00. The present study provides baseline data that could be valuable for proper environmental management and policy-making to reduce the myriad influx of heavy metal contamination in the study area. To provide a thorough understanding of metal pollution in the Nsuta community, future research on metal speciation, bioavailability, bioaccumulation, potential modes of action in soils, and the implications for human health is also necessary.
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