Spatial and Temporal Distribution of Dust‐Bound Trace Metal Elements around Kuhdasht Watershed Area in Iran

Dust, as a source of trace metal elements, affects the health of society. The spatial and temporal concentrations of dust‐bound trace metals (Cd, Pb, Ni, Zn, Cu, and Mn) in Kuhdasht watershed (456 km²), Lorestan Province, Iran, is investigated. Dust is collected using glass traps placed in ten research stations in the region. The spatial and temporal distribution of dust trace metals are plotted using ARC‐GIS. The highest and the lowest concentrations of Zn (9751150 mg kg^?1), Pb (46.352.9 mg kg^?1), and Cd (2.443.30 mg kg^?1) are obtained in winter, of Ni (98110 mg kg^?1) and Cu in autumn (16.053.5 mg kg^?1), and of Mn in summer (385505 mg kg^?1). The spatial concentrations of dust‐bound trace metals indicate all, except Cu, show a decreasing trend from the mountains toward the plains, similar to that of soil and of dust, except for Zn, which shows higher concentrations in dust than in soil. The potential sources of dust‐bound trace metals and their rate of contamination are also investigated using the enrichment and contamination factors. The major sources of Cd and Zn in the dust of watershed are due to anthropogenic activities or from activities outside the borders.     

太湖流域西氿湖沉积岩芯中重金属污染及潜在生态风险

通过对太湖流域西沈湖沉积物岩芯XJ2中Cu、Pb、Zn、Cd、Cr等5种重金属元素总量的分析,结合测年结果,揭示了不同时间段重金属污染物的分布特征,并利用Hakansen潜在生态风险评价法对沉积物岩芯的污染状况及潜在生态风险的历史变化进行了研究.结果表明岩芯受Cd元素污染最重,其它4种元素较Cd则轻得多,因此Cd元素是影响该地区沉积物潜在生态风险的绝对主导因素.从20世纪初叶开始,沉积物中的重金属元素污染及其相应的潜在生态风险开始上升,并且上升幅度不断加剧,到20世纪90年代达到最大值,沉积物污染及潜在生态风险级别均为"很高",随后便开始迅速下降,然而直到2004年这两个参数仍然维持在"很高"级别.     

城市道路尘埃的磁性特征及其环境意义

城市环境磁性研究表明,道路尘埃中的粗颗粒磁性载体(频率磁化率系数χ′FD＜5%)多为人为源,磁性矿物以单畴和多畴状态的磁铁矿为主,同时含有少量的赤铁矿和其他磁性矿物;细颗粒磁性载体(χ′FD为7%～11%)多为自然源,磁化率较低(小于100×10-8 m3/kg).磁性物质在迁移时往往与粗一级粒径的尘埃颗粒相伴生,磁性参数(如磁化率)和重金属元素(如铅、锌)质量分数之间呈相关关系,它们之间的关系可以用回归分析方法确定.利用电镜分析、因子分析和聚类分析方法可以识别道路尘埃物质的污染源.因此,道路尘埃的磁性特征研究在城市环境评价中具有潜在的重要意义.     

Contamination of shallow aquifers by arsenic in upper reaches of Tista river at Siliguri–Jalpaiguri area of West Bengal, India

Arsenic is present in groundwater at Siliguri–Jalpaiguri area, West Bengal, India. This is the place where Tista river descending from the Himalayas meets the alluvial plain. The area represents alluvial fan and floodplains of Tista, Mahananda-Balasan, Jaladhaka and its tributaries. In the river sediment samples, para- and ferro-magnetic minerals within 0.3–0.05 mm fraction contain 9–80 ppm of arsenic. The study indicates that iron bearing minerals viz. biotite, hornblende as well as iron coated grains of the sediment are major contributors towards arsenic budget. Though magnetite as a mineral shows maximum arsenic content (22 ppm), it is volumetrically not of much significance. Measurement of groundwater collected from tube wells shows up to 0.05 ppm of arsenic. These arsenic contaminated tube wells occur in a linear fashion along the course of the rivers. Moreover, localization of contaminated tube wells coincides with the change of channel gradient as observed in longitudinal section. The study enumerates a cause–effect relationship of arsenic occurrence with river gradient and fluvial sedimentation.     

Analysis of resistivity data obtained from cone penetrometer in contaminated soil layers

In horizontally layered soils of different electrical properties, electrical potential distribution becomes complex and the obtained resistivity data may be limited in reflecting the actual soil profile. Thus the objective of this study was to identify the factors that affect resistivity measurement on the cone penetrometer and further investigate the sensitivity of measured resistivity to different types and concentrations of contaminants at the subsurface level. First, a theoretical resistivity equation was derived to provide a means of computing the geometric factor. The effective volume of measurement on the cone penetrometer was investigated and laboratory soil box tests verified the dominance of partially high resistivity regions within the effective volume of measurement over the apparent resistivity. Such effect was found to lead to possible discrepancies between the recorded resistivity data and the actual depth of measurement. Measurements on contaminated soil layers indicated that resistivity cones are efffective in delineating inorganic contaminants in soils of high water contents, and detecting NAPLs floating above the groundwater table provided that soils adjacent to the plume are not dry of water. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Nutrient chemistry and salinity mapping of the Delhi aquifer,India: source identification perspective

Present study is an effort to distinguish between the contributions of natural weathering and anthropogenic inputs towards high salinity and nutrient concentrations in the groundwater of National Capital Territory (NCT) Delhi, India. Apart from the source identification, the aquifer of entire territory has been characterized and mapped on the basis of salinity in space and water suitability with its depth. Major element chemistry, conventional graphical plots and specific ionic ratio of Na⁺/Cl⁻, SO₄ ²⁻/Cl⁻, Mg²⁺/Ca²⁺ and Ca²⁺/(HCO₃ ⁻ + SO₄ ²⁻) are conjointly used to distinguish different salinization sources. Results suggest that leaching from the various unlined landfill sites and drains is the prime cause of NO₃ ⁻ contamination while study area is highly affected with inland salinity which is geogenic in origin. The seasonal water level fluctuation and rising water level increases nutrients concentration in groundwater. Mixing with old saline sub-surface groundwater and dissolution of surface salts in the salt affected soil areas were identified as the principle processes controlling groundwater salinity through comparison of ionic ratio. Only minor increase of salinity is the result of evaporation effect and pollution inflows. The entire territory has characterized into four groups as fresh, freshening, near freshening and saline with respect to salinity in groundwater. The salinity mapping suggests that in general, for drinking needs, groundwater in the fresh, freshening and near freshening zone is suitable up to a depth of 45, 20 and 12 m, respectively, while the saline zones are unsuitable for any domestic use. In the consideration of increasing demand of drinking water in the area; present study is vital and recommends further isotopic investigations and highlights the need of immediate management action for landfill sites and unlined drains.     

Contamination,chemical speciation and vertical distribution of heavy metals in soils of an old and large industrial zone in Northeast China

Heavy metal pollution of soils has become a major concern in China as a consequence of rapid urbanization and industrialization in recent years. However, the evaluation on soil heavy metal pollution in Shenyang, the largest heavy industrial base city in China, has not yet been conducted. In this study, accumulation, chemical speciation, and vertical distribution Cu, Zn, Pb and Cd in soils were studied and pollution condition was assessed in Tiexi Industrial District of Shenyang, the largest and oldest industrial zone in Northeastern China. The results showed that in topsoil, the average concentration of total Cu, Zn, Pb, and Cd was 209.06, 599.92, 470.19 and 8.59 mg kg⁻¹, respectively, much higher than the national threshold limit. The values of pollution index and integrated pollution index showed that the pollution level was Cd > Cu > Zn > Pb, and Cd, Cu and Zn belong to heavy pollution level. The residual, Fe and Mn oxide-bound, and organic-bound species accounted for about 90%, while carbonate-bound and exchangeable species accounted for about 10%. This study indicates that the soils in the industrial zone were widely and extremely polluted by multi-heavy metals as a result of long-term industrial activities.     

108国道和魏刘河对绵阳魏城土壤重金属积累影响的研究

通过对108国道和潼江支流魏刘河二侧土壤中重金属元素的富集系数（EF）计算研究,总结了该研究区公路（Ro型）和河流（Rv型）二种EF值典型特征,同时指出该研究区河流为污染源的贡献者,而公路通过改变土壤物理结构,造成污染的程度增大。     

黄土对Cr(III)的吸附特性及机理研究

铬是一种重金属痕量元素,人体通过食物链摄入过量的铬会在人体内富集,随之产生中毒反应。研究Cr(III)的浓度、反应时间、反应温度、pH值等因素对Cr(III)在黄土上吸附特性的影响,结果表明黄土对Cr(III)的吸附非常迅速,并且吸附量非常大,等温吸附模型Freundlich和Dubinin-Radushkevich(D-R)模型都能很好地解释Cr(III)在黄土上的吸附过程。热动力学分析表明,吸附是一个自发的过程,升温可促进吸附作用的进行。随着温度的不断升高,Cr(III)的吸附量逐渐增大。溶液的pH值是影响Cr(III)吸附效果的一个重要因素,当pH>6时,Cr(III)几乎完全被去除。利用X光衍射图谱和红外光谱分析,探讨黄土与Cr(III)的结合机制,黄土中的高岭土、石英等黏土矿物以及有机质成分对吸附过程起重要作用。