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普拉河及其支流沉积物中的重金属污染评估

Assessment of Heavy Metal Pollution in the Sediments of the River Pra and Its Tributaries.

作者信息

Duncan Albert Ebo, de Vries Nanne, Nyarko Kwabena Biritwum

机构信息

1Department of Health Promotion, Faculty of Health Medicine and Life Sciences, Maastricht University, B1, 120 Maastricht, Netherlands.

2Department of Civil Engineering, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

出版信息

Water Air Soil Pollut. 2018;229(8):272. doi: 10.1007/s11270-018-3899-6. Epub 2018 Aug 6.

Abstract

An investigative study was conducted to determine the heavy metal pollution in the sediment in the Pra Basin of Ghana from 27 sampling points during the dry and wet seasons using the geo-accumulation index (Igeo), enrichment factor (EF), and pollution load index (PLI). Sediments were acid digested and analyzed for the following selected metals: arsenic (As), lead (Pb), cadmium (Cd), zinc (Zn), manganese (Mn), total chromium (Cr), nickel (Ni), and iron (Fe) using the dual atomizer and hydride generator atomic absorption spectrophotometer (model ASC-7000 No A309654, Shimadzu, Japan). The metal concentrations (mg kg) in the sediments were as follows: As (0.175) < Cd (3.206) < Ni (79.927) < Zn (118.323) < Cr (216.708) < Mn (234.742) < Pb (335.381) < Fe (1354.513) in the dry season and As (0.002) < Cd (7.279) < Ni (72.663) < Zn (35.622) < Pb (135.863) < Cr (167.604) < Mn (183.904) < Fe (1138.551) for the wet season. The EF which is an indication of whether metal concentrations are due to anthropogenic activities shows enrichment at all site for the metals Cr, Pb, and Cd in the wet seasons. However, only 4 out of the 27 sites showed Ni enrichment in the wet season. Contrary to the wet season, only Pb and Cr recorded enrichment at all sites during the dry season. Fifteen out of the 27 sites recorded Cd enrichment and 24 out of the 27 sites recorded Ni enriched during the dry season. None of the sites were enriched with Fe, As, Zn, and Mn in either the dry or wet seasons. For both dry and wet seasons, the pollution load index for all the sites except one was at the background levels which is a sign of non-deterioration of the sites studied. In the wet season, the calculated Igeo reveals that the study area is not contaminated with respect to As, Zn, Fe, and Mn; uncontaminated to moderately contaminated with Cd; moderately contaminated with Cr; uncontaminated to moderately to heavily contaminated with Ni; and moderately to heavily contaminated with Pb. The dry season Igeo results reveal non-contamination of the study area with respect to As, Fe, and Mn; uncontaminated to moderately contaminated with Zn; moderately contaminated with Cr; uncontaminated to heavily contaminated with Cd; uncontaminated to extremely contaminated with Ni; and moderately to extremely contaminated with Pb. The high levels of Cd, Pb, and Cr in all the sites are due to unregulated illegal mining activities occurring in and around the study area. It is hoped that this study will prompt the basin management board to improve their management strategies in controlling unregulated illegal mining in the basin sediments.

摘要

开展了一项调查研究,以使用地累积指数(Igeo)、富集因子(EF)和污染负荷指数(PLI),确定加纳普拉盆地旱季和雨季27个采样点沉积物中的重金属污染情况。沉积物经酸消解后,使用双原子化器和氢化物发生器原子吸收分光光度计(型号ASC - 7000,编号A309654,日本岛津公司)分析以下选定金属:砷(As)、铅(Pb)、镉(Cd)、锌(Zn)、锰(Mn)、总铬(Cr)、镍(Ni)和铁(Fe)。旱季沉积物中的金属浓度(mg/kg)如下:As(0.175)<Cd(3.206)<Ni(79.927)<Zn(118.323)<Cr(216.708)<Mn(234.742)<Pb(335.381)<Fe(1354.513);雨季为:As(0.002)<Cd(7.279)<Ni(72.663)<Zn(35.622)<Pb(135.863)<Cr(167.604)<Mn(183.904)<Fe(1138.551)。EF表明金属浓度是否归因于人为活动,结果显示雨季所有采样点的Cr、Pb和Cd金属出现富集。然而,27个采样点中只有4个在雨季显示出Ni富集。与雨季相反,旱季只有Pb和Cr在所有采样点出现富集。27个采样点中有15个在旱季记录到Cd富集,24个记录到Ni富集。旱季和雨季均没有采样点出现Fe、As、Zn和Mn富集。对于旱季和雨季,除一个采样点外,所有采样点的污染负荷指数均处于背景水平,这表明所研究的采样点没有恶化迹象。在雨季,计算得出的Igeo表明,研究区域As、Zn、Fe和Mn未受污染;Cd未受污染至中度污染;Cr中度污染;Ni未受污染至中度至重度污染;Pb中度至重度污染。旱季Igeo结果表明,研究区域As、Fe和Mn未受污染;Zn未受污染至中度污染;Cr中度污染;Cd未受污染至重度污染;Ni未受污染至极度污染;Pb中度至极度污染。所有采样点中Cd、Pb和Cr含量高是由于研究区域及其周边存在无监管的非法采矿活动。希望本研究将促使流域管理委员会改进其管理策略,以控制流域沉积物中的无监管非法采矿活动。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/6096550/3fc3a409ae23/11270_2018_3899_Fig1_HTML.jpg

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