常州某农药生产场地土壤中挥发性有机物污染状况调查

对常州某农药生产场地土壤中挥发性有机物污染状况进行了调查。数据表明,该场地土壤中挥发性有机物污染以苯系物和卤代烃为主。苯系物浓度为0～56.7mg/kg,卤代烃浓度为0～1.14mg/kg,有潜在风险。     

镇江地区土壤样品中重金属Cd含量与空间分布

通过对镇江地区土壤样品中 Cd 监测结果统计分析表明，全市69个样品中 Cd 质量比范围为0．06 mg/kg ～1．37 mg/kg，均值为0．23 mg/kg，与全国背景值相比，有一定程度富集；样品中 Cd 质量比成偏态分布，相对标准偏差较大。选用单项污染指数法对 Cd污染程度评价表明，镇江地区83％的土壤样品未受到 Cd 污染，14％为轻度污染，3％为中度污染。结合镇江地区的产业结构分析，电镀行业是土壤 Cd 污染的主要来源，道路运输、农药化肥在一定程度上也加重了污染。     

生活垃圾焚烧发电厂周边环境二噁英污染水平及人群暴露评估

选取某典型生活垃圾焚烧发电厂为研究对象,监测其周边环境空气、土壤、地下水、农作物等环境介质中二噁英的浓度水平,初步评估周边人群二噁英暴露水平。研究结果表明,该厂周边环境空气、土壤、地下水中二噁英测定值分别为0. 236 pg TEQ/m3～0. 331 pg TEQ/m3、1. 94 ng TEQ/kg～2. 71 ng TEQ/kg、0. 17 pg TEQ/L～0. 26 pg TEQ/L,企业排放的二噁英对周边环境影响较小;成人和儿童在暴露介质中摄入二噁英总量分别为0. 959 pg TEQ/(kg·d)和1. 59 pg TEQ/(kg·d),均低于4 pg TEQ/(kg·d)的标准,经大米和面粉摄入二噁英的量超过总暴露量的90%,提示食物是人群二噁英暴露的主要介质。     

某灌区土壤中重金属镉污染调查

对沈阳市郊某污灌区土壤中重金属镉的污染状况进行了调查.结果表明,2000年土壤中镉质量比为0.23 mg/kg～5.55 mg/kg,最高值超标17.5倍;平均值为2.02 mg/kg,属严重污染,污染程度仍处在停耕前水平;污灌区土壤镉含量与土壤深度有关,深度为16 cm～30 cm污染最重,51 cm～80 cm污染最轻.     

污染土壤中六价铬的测定

通过加入碱性消解液、MgCl2和磷酸缓冲溶液,建立了污染土壤中六价铬的分光光度测定法.方法在0 mg/L～0.200 mg/L范围内线性良好,检出限为0.16 mg/kg(以2.5 g样品计),土壤样品测定的RSD为4.6%,加标回收率为92.3%～107%.     

全自动石墨消解-原子荧光法测定土壤总汞

采用全自动石墨消解-原子荧光光度法对土壤总汞进行测定,确定最佳消解时间为1 h,消解液最佳用量为8.0 m L。方法在总汞质量浓度为0.2~2.0μg/L范围内具有良好的线性,相关系数为0.999 9,当取样量为0.500 0 g时,检出限为0.002 mg/kg;测定不同标准土壤样品总汞的结果均在保证值范围内,精密度为4.0%~7.0%,加标回收率为95.0%~108.5%;对甘肃省实际土壤及沉积物样品测定进一步验证了方法的适用性。该法适合大批量样品分析,对于提高工作效率有重要意义。     

安徽某燃煤电厂周边土壤汞分布特征及风险评价

结合当地气象条件,采集了安徽某燃煤电厂周边地区的土壤,采用冷原子吸收法测定其汞含量,应用地统计学和地理信息系统方法分析了电厂周边表层土壤汞含量的空间分布特性,分析了土壤中汞与理化性质之间的相关性,并进行了风险评价。结果表明,电厂周边表层土壤汞含量范围为0.015~0.076 mg/kg,平均值为0.029 mg/kg,虽未超过国家允许的标准,但与当地背景值及安徽省土壤汞含量相比均有一定程度的增加;土壤汞含量的总体分布特征为除距排放源1~2 km的环形区域受影响最大外,污染程度随着与电厂距离的增大而递减,汞含量空间分布受主导风向影响呈现明显的条带分布。相比于单因子污染指数法和地累积指数法,潜在生态危害指数评价法能更好地反映燃煤电厂周围土壤中汞的污染水平和生态风险程度。土壤汞含量与土壤理化性质之间存在不同程度的相关性。     

微波消解-原子荧光法测定土壤中汞、砷、硒

建立了微波消解-原子荧光法测定土壤中汞、砷、硒的方法.汞在0.00 μg/L～1.00 μg/L、砷在0.00 μg/L～10.0 μg/L、硒在0.00 μg/L～2.00 μg/L之间线性关系良好,以称样0.200 0 g计,检出限汞为0.005 mg/kg,砷为0.009 mg/kg,硒为0.025 mg/kg.经国家有证标准物质验证,方法精密度与准确度均能满足土壤环境样品的测试要求.     

油菜对铅镉污染土壤的修复效果研究

文章通过盆栽实验分析油菜在不同浓度下对土壤中铅、镉的富集能力,分别配制Pb+Cd浓度为0mg/kg+0mg/kg、200mg/kg+5mg/kg、500mg/kg+10mg/kg、1000mg/kg+15mg/kg、1500mg/kg+20mg/kg的5种模拟污染土壤,种植油菜5个月后收获,通过测定土壤中Pb、Cd的浓度,油菜地上部分、地下部分Pb、Cd的含量,油菜各部位的转运系数和富集系数,结果表明:油菜对土壤Pb、Cd污染具有一定的耐性,在土壤Pb浓度0~200mg/kg、Cd浓度0~5mg/kg范围内,对油菜的生长有促进作用。在土壤Pb浓度200~1500mg/kg、Cd浓度5~20mg/kg范围内,对油菜的生长有抑制作用。油菜根部、茎叶中和籽粒中对Pb的富集系数分别为8.92、11.19和7.66,对Cd的富集系数分别为59.01、80.44和52.42,油菜茎叶对Pb、Cd的富集能力最强。     

高效液相色谱法测定稻田中丙草胺残留

用二氯甲烷提取稻田水和水稻植株样品中的丙草胺，稻田土壤样品用二氯甲烷-甲醇混合溶剂（体积比为9∶1）提取，再用高效液相色谱仪测定。方法在0．02 mg/L～2．00 mg/L的范围内线性良好，相关系数为0．9998；稻田水、土壤，水稻植株中丙草胺的检出限分别为0．001 mg/L、0．005 mg/kg、0．01 mg/kg；对稻田水、土壤和水稻植株分别做3个浓度水平的加标回收试验，重复5次，平均回收率在75．5％～84．7％之间，测定结果的相对标准偏差为2．0％～10．5％。     

天津城郊土壤中PAHs含量特征及来源解析

以天津市郊环城四区为研究对象,系统采集了环城四区95个表层土壤样品,利用高效液相色谱仪对16种PAHs进行分析测定,结果表明,西青、东丽、津南和北辰土壤中16种PAHs的总量范围分别为62.6～1 994.9、36.1～4 074.7、20.1～2 502.5、22.1～707.7μg/kg;平均含量分别为445.8、841.8、509.5、242.5μg/kg。四区中都以高环多环芳烃为主,西青、东丽、北辰和津南高环多环芳烃分别占多环芳烃总比例的45.4%、42.2%、38.8%和38.7%。空间分析的结果表明,靠近天津市市区样点土壤中多环芳烃的含量要明显高于远离市区土壤中多环芳烃的含量。利用环数PAHs的相对丰度和比值法对天津市郊环城四区土壤中多环芳烃的污染来源进行了解析,研究区土壤监测样点的PAHs主要来自燃烧源,少部分来自石油类来源或几种污染源的共同复合累加的作用。     

Risk assessment and distribution of soil Pb in Guangdong, China

In this study, the spatial distributions of soil lead (Pb) concentration in three horizontal soils in Guangdong, China, were surveyed and analyzed using geostatistics and geography information systems (GIS). Findings indicated that the Pb geometric mean concentration of 23.3 mg/kg in surface soils was found to be higher than those in global soils, which ranged from 2.3–235 mg/kg. In addition, the Pb geometric mean concentrations from A- to C-horizon were found to be 23.3, 27.2, and 28.6 mg/kg, respectively. The classification of a soil Pb environmental risk in an area was likewise presented based on the different levels of environmental quality of Pb and was done by GIS technology. Accordingly, there is a higher local concentration of Pb in the surrounding areas of Guangzhou where there is higher population density and in the north of Guangdong, which is a historic mining area. The results obtained by the environmental risk assessment reveal that about 46% of total surveyed area was above the background value, that is, 2.7% of the total area was at risk of pollution.     

Assessment of carcinogenic heavy metal levels in Brazilian cigarettes

Total mercury (Hg(T)) and bioavailability Hg (Hg(HCl)) concentrations in soil were determined in five districts in Wuhu urban area. Spatial pattern of soil Hg concentration was generated through kriging technology. Results showed that Hg concentration in soil ranged from 0.024 to 2.844 mg kg(?-1) with an average of 0.207 mg kg(?-1). Hg concentration in soil appeared to have a block distribution and decreased from downtown to surrounding district. And Hg concentrations appeared to have a medium scale spatial auto correlation, strongly affected by human activity. The maximal Hg average concentration (0.332 mg kg(?-1)) in soil appeared in Jinghu district, where the high intensity of human activities is. Second highest Hg average concentration (0.263 mg kg(?-1)) in soil appeared in development district, where the intensive industrial activities are. Bioavailability Hg concentration in soil ranged from 2.6 to 4.9 μg kg(?-1) with an average of 3.8 μg kg(?-1), which had a ratio of 0.28~6.44% to total Hg. The ratios of bioavailability Hg to total Hg in vegetable soil were bigger than those of park soil. Correlation analysis showed that total Hg, organic matter, total phosphorus, and bioavailability Hg concentrations in soil were significantly positively correlated. Hg concentration in vegetable ranged from 2.7 to 15.2 μg kg(?-1) with an average of 6.5 μg kg(?-1). Hg concentration in vegetable was positively correlated with Hg(HCl) concentration in soil. According to the calculation on hazard quotient (HQ) for children, inhalation of Hg vapor from soil is the main exposure pathway, in which HQ is 2.517 × 10(?-2), accounting for 80.3% of the four exposure pathways. Hazard index (HI) of the four exposure pathways is lower than the "safe" level of HI = 1; therefore, exposure of soil Hg exhibited little potential health risk to children in Wuhu urban area.     

Speciation of mercury in mine waste: case study of abandoned and active gold mine sites at the Bibiani–Anwiaso–Bekwai area of South Western Ghana

Speciation determines toxicity, transport pathways and residence time of a metal in different compartments of the environment. This study investigated the speciation of mercury in soils, derived from sites known for dumping of mine wastes in the Bibiani–Anwiaso–Bekwai district, a gold mining community of the Western Region of Ghana. Soil samples were taken from the surface; depths of 20, 40 and 60?cm from mine waste at both abandoned and active mine sites. Each sample was analysed for total mercury, organic mercury and elemental mercury. After sample treatment, digestion and reduction with stannous chloride (SnCl₂), total mercury content was determined using the Inductively Coupled Plasma—Optical Emissions Spectrometer (ICP–OES). Organic mercury content was determined employing a differential technique after disposing of elemental mercury by heating. Total mercury content in samples ranged from 0.067 to 0.876?mg/kg for surface soils. The same soil of depths 20, 40 and 60?cm had total mercury from 0.102 to 1.066, 0.037 to 4.037 and 0.191 to 4.998?mg/kg, respectively. For organic mercury, concentrations range from 0.012 to 0.260?mg/kg for surface soil. Soil depths of 20, 40 and 60?cm had organic mercury concentrations from 0.016 to 0.653, 0.041 to 1.093 and 0.101 to 2.546?mg/kg respectively. Elemental mercury concentrations in surface soils, soils at depths of 20, 40 and 60 cm ranged from 0.043 to 0.780; 0.017 to 0.749; 0.014 to 2.944 and 0.009 to 2.452 mg/kg respectively. Among the sites studied, only galamsey tailings (GM) showed a trend of increasing total mercury level with increasing depth. For the other sites, trends were not defined. There has been no defined trend for elemental mercury with depth at any of the sampling sites. Just as with total mercury, it was only GM that showed an increasing trend of organic mercury concentration with depth.     

Distributions, sources and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in topsoil at Ji’nan city, China

Surface soil (0-5 cm) samples from 17 sampling sites including different functional areas at Ji'nan city in Shandong Province of China were collected and analyzed for 16 EPA priority polycyclic aromatic hydrocarbons (PAHs). The total PAH concentrations were in the range from 1.31 mg kg(-1) to 254.08 mg kg(-1) (dry weight), and the average level of total PAHs was 23.25 mg kg(-1). The highest total PAHs concentrations were found in steel and iron plant at industrial areas. The total PAHs concentrations in industrial areas were markedly higher than those in other different functional areas. According to comparing total PAHs concentration in Ji'nan city to that of other urban areas, it was found that total PAHs concentrations were 6 to 137 times higher than other areas because of some specific sampling sites such as steel and iron plant and one main roadside. The results showed that PAHs in topsoil of Ji'nan city were suffered from strong pyrogenic influence, especially in industrial areas. However about 52.9% soil samples were mainly originated from both pyrogenic and petrogenic mixed sources based on Flu/Pyr ratios and Phe/Ant ratios. Furthermore, It was found that all individual PAHs except Fle were significantly correlated (P < 0.01) with LMW, HMW, total PAHs and SOM, and individual PAHs except Fle in soils were significantly correlated (P < 0.01) with each other. The nemerow composite index to assess the environmental quality showed that the soil sample of steel and iron plant in industrial areas and one main roadside were heavy pollution of PAHs, and about 47% soil sampling sites were safety, about 53% soil sampling sites were got different grades of PAHs pollution.     

Heavy metal contamination of urban soils and dusts in Guangzhou, South China

The heavy metal concentrations of soil and dust samples from roadside, residential areas, parks, campus sport grounds, and commercial sites were studied in Guangzhou, South China. Heavy metals in samples were determined by inductively coupled plasma atomic emission spectrophotometer following acidic digestion with HClO₄ + HF + HNO₃. High concentrations, especially of Cd, Pb, and Zn, were found with mean concentrations of Cd, Cr, Cu, Ni, Pb, and Zn in the urban dusts being 4.22?±?1.21, 62.2?±?27.1, 116?±?30, 31.9?±?12.6, 72.6?±?17.9, and 504?±?191 mg/kg dry weight, respectively. The respective levels in urban soils (0.23?±?0.19, 22.4?±?13.8, 41.6?±?29.4, 11.1?±?5.3, 65.4?±?40.2, and 277?±?214 mg/kg dry weight, respectively), were significantly lower. The integrated pollution index of six metals varied from 0.25 to 3.4 and from 2.5 to 8.4 in urban soils and dusts, respectively, with 61 % of urban soil samples being classified as moderately to highly polluted and all dust samples being classified as highly polluted. The statistical analysis results for the urban dust showed good agreement between principal component analysis and cluster analysis, but distinctly different elemental associations and clustering patterns were observed among heavy metals in the urban soils. The results of multivariate statistic analysis indicated that Cr and Ni concentrations were mainly of natural origin, while Cd, Cu, Pb, and Zn were derived from anthropogenic activities.     

Small mammals as biomonitors of metal pollution: a case study in Slovenia

The transfer of lead, cadmium, zinc, mercury, copper and molybdenum from soil to the tissues of small mammals inhabiting differently polluted areas in Slovenia was investigated. Metals were determined in soil samples and in the livers of 139 individuals of five small mammal species, collected in 2012 in the vicinity of a former lead smelter, the largest Slovenian thermal power plant, along a main road and in a control area. The area in the vicinity of former lead smelter differs considerably from other study areas. The soil from that area is heavily polluted with Pb and Cd. The mean metal concentrations in the liver, irrespective of species, varied in the following ranges—Pb: 0.40–7.40 mg/kg fw and Cd: 0.27–135 mg/kg fw and reached effect concentrations at which toxic effects can be expected in a significant proportion of the livers of the small mammal specimens (Pb 40 %, Cd 67 %). These findings indicate that the majority of small mammals trapped in the area of the former lead smelter are at risk of toxic effects due to the very high bioaccumulation of Pb and Cd in the organism. On the contrary, Pd and Cd concentrations in the livers of small mammals sampled in the vicinity of the thermal power plant and along the main road were comparable with reference values and considerably lower than effect concentrations. Additionally, the study suggests that Apodemus flavicollis and Myodes glareolus are very suitable biomonitors of metal pollution.     

Total mercury determination in sand boxes from Montreal

Direct mercury analysis was successfully applied to determine trace levels of total mercury in samples from sand boxes in Montréal (Québec, Canada). Twenty sand boxes were sampled from across the city and divided into two size fractions, a fine fraction (<100 microm) and a whole fraction. The concentrations of mercury ranged from 1.6 to 35 microg Hg kg(-1) dry soil for the fine fraction and from 0.7 to 6 microg Hg kg(-1) dry soil for the whole fraction. The mercury concentrations correlated with the soil organic carbon content (R2= 0.67) in the sand. The ratio of the concentration of mercury in the fine over the whole fraction varied from 2.2 to 18. Using published soil ingestion rates for children, the calculated daily intake values varied from 0 to 0.5 ng Hg kg(-1) bw d(-1) with an estimated oral ingestion of 200 mg of sand and from 0.2 to 4.7 ng Hg kg(-1) bw d(-1) with an ingestion of 1750 mg of sand. None of the sand boxes contain sufficient amounts of mercury so as to exceed the currently accepted daily intake threshold of 0.105 microg Hg kg(-1) bw d(-1) established by Health Canada.     

贵州省部分地区土壤中酞酸酯类污染现状调查

对贵州省部分地区表层土壤中酞酸酯类的污染状况进行了调查。分别在遵义地区、黔南地区、黔东南地区和毕节地区采集483个土壤样品分析,结果表明,样品中酞酸酯总质量比(ΣPAEs)为未检出~8.22 mg/kg,均值为0.63 mg/kg。其中DEHP和DBP为主要污染物,均值分别为0.32 mg/kg和0.24 mg/kg,检出率分别为90.89%和97.10%。     

Total mercury loadings in sediment from gold mining and conservation areas in Guyana

The Low Carbon Development Strategy proposed in June 2009 by the government of Guyana in response to the Reducing Emissions from Deforestation and Forest Degradation in Developing Countries program has triggered evaluation of forest-related activities, thereby acting as a catalyst for improvements in Guyana's small- to medium-scale gold mining industry. This has also shed light on areas committed to conservation, something that has also been handled by Non Governmental Organizations. This paper compares water quality and mercury concentrations in sediment from four main areas in Guyana, two that are heavily mined for gold using mercury amalgamation methods (Arakaka and Mahdia) and two that are considered conservation areas (Iwokrama and Konashen). Fifty-three sediment and soil mercury loadings ranged from 29 to 1,200 ng/g and averaged 215 ± 187 ng/g for all sites with similar averages in conservation and mining areas. Sediment loadings are within the range seen in French Guiana and Suriname, but conservation area samples had higher loadings than the corresponding uncontaminated baselines. Type of ore and location in the mining process seemed to influence mercury loadings. Mercury sediment loadings were slightly positively correlated with pH (correlation coefficient = 0.2; p value < 0.001) whereas no significant correlations were found with dissolved oxygen or turbidity.