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1.
An investigation was conducted to study the baseline levels of Ba, Cd, Cu, Cr, Ni, Pb, Sr, V and Zn (aqua regia-extractable) based on 51 representative soils of the Torrelles and Sant Climent Municipal Districts (Catalonia, Spain). The baseline concentrations of those elements were (mg kg−1): Ba 73.9–617.9, Cr 9.2–120.2, Cu 4.0–111.6, Ni 6.1–118.6, Pb 5.6–217.5, Sr 19.6–128.8, V 12.1–101.2, and Zn 16.8–326.8, respectively.Forty-nine samples were reported as having less than the 0.67 mg kg−1 detection limit for cadmiun and were therefore not useful for baseline determination; however, these results suggest that the baseline average is probably below 0.67 mg kg−1.Upper baseline values for most of the elements corresponded with those reported in the literature, except for Pb and Zn, which were two to four times greater.Soil properties, including clay fraction, OC, CEC and pHw were related to metal concentration using correlation and factorial analysis. R-mode factor analysis separates the soil analysis data into three factors. These factors explain 67.3% of the total variance, suggesting that metal concentration was controlled by soil composition.  相似文献   

2.
Anthropogenic sources of pollution can significantly contribute to elevated concentrations of toxic elements in soils. A preliminary survey of trace elements content and their availability in residential soils from New Madrid County, Missouri was undertaken. Mean elemental concentrations (mg kg−1, dry wt) of sixty two soil samples were: As 6.6, Be 0.8, Cd 1.6, Co 9.7, Cr 24.5, Cu 18.1, Fe 9951, Mn 298, Ni 15.6, Pb 48.8, V 42.1, Zn 95.5 and Hg 0.05. The US EPA preliminary remediation goals (PRGs) was only exceeded by As (7 % of samples) and V (8% of samples). The Missouri average background values were exceeded by Pb (69%), Zn (31%), Cu (27%), As (23%), Be (19%), Co (18%), Ni (16%), V (8%) and Mn (2%). Crustal enrichments (EFc) for As (97), Cr (6), Cu (10), Pb (121), V (7), and Hg (17) were highest for North Lilbourn soils. Fractionation experiment revealed that Fe (54–79%) was in the residual phase while Zn (70–90%), Mn (88–92%), As (59–81%) and Pb (63–79%) were potentially available in soils. Factor loadings of the element concentrations on principal components 1, 2 and 3 accounted for over 81% variance of the data set. The factor loadings suggested that apart from natural contributions of trace elements to the soils, human activities possibly accounted for other inputs in soils.  相似文献   

3.
Among commonly employed methods of fast estimation of the soil biological activity a method of the oxygen consumption determination is used. The main goal of this research was an estimation of a soil respiratory metabolism using the constant pressure volumetric respirometer and also using the flow-through respirometer UNI-RES10.Soil respiration measurements were done using both types of respirometers in temperatures 10, 15, 20, 25, 30 and 35 °C, keeping up the constant humidity. The investigated soil was a soil humus belonged to organic soils from the Dziekanów Leny field. The soil respiration was also measured for 8 plant communities in Sudeten Mountains with various respiration intensity.After the experiments it was stated that both measuring instruments could be used for the soil metabolism evaluation. Readouts obtained from the UNI-RES10 respirometer are smaller then readouts when using the constant pressure volumetric respirometer. The flow-through respirometers have to be calibrated to obtain results comparable with these from volumetric ones. The volumetric and flow-through respirometry methods are useful for the comparative analysis of metabolism levels.  相似文献   

4.
分析和评价典型涉污企业周边土壤环境质量,对于加强企业用地环境风险管控,实施土壤重金属污染精准防控,进一步保障农产品质量安全具有重要意义。以18类典型涉污企业周边土壤为研究对象,对475家企业周边的2 017个监测样点进行土壤重金属Cd、As、Pb、Hg、Cr、Cu、Zn和Ni元素含量测定,并采用主成分分析法、Hakanson 潜在生态风险指数法进行分析及评价。结果表明:典型涉污企业周边土壤重金属污染以Cd、Pb和As元素为主,各元素含量超过土壤污染风险筛选值的样品比例为9.82%~31.0%,超过土壤污染风险管控值的样品比例为4.46%~13.1%,其次是Zn、Cu、Hg和Ni,Cr无明显污染;主要污染元素Cd、Pb、As、Zn和Cu来自相同污染源且主要分布在有色金属矿采选业(B9)、黑色金属冶炼和压延加工业(C31)、有色金属冶炼和压延加工业(C32)、生态保护和环境治理业(N77)等行业企业周边;黑色金属冶炼和压延加工业(C31)、有色金属矿采选业(B9)、有色金属冶炼和压延加工业(C32)等行业企业周边土壤重金属潜在生态风险等级较高,中等风险及以上比例分别为76.0%、53.0%和54.1%。可见,典型涉污企业周边土壤重金属存在一定程度的污染,尤其是有色金属矿采选业(B9)等采矿业以及黑色金属冶炼和压延加工(C31)等制造业等,污染程度高,潜在生态风险大,需要加强监测和管控。  相似文献   

5.
董铮  王琳  田芳 《干旱环境监测》2014,28(4):149-153
为了锯镇江地区土壤中重金属Cu和Ph的污染状况与空间分布,对镇江地区表层土壤中的Cu和Pb进行了采样监测。结果表明,镇江地区表层土壤中cu的含量为19.2~273mg/kg,Pb的含量为20.6~3846mg/kg。与全省土壤背景值相比,均有一定程度的富集。对cu和Pb的相互关系进行分析可得出,镇江地区土壤在一定程度上受到农业面源的污染。  相似文献   

6.
以钢丝绳产业集聚区内的土壤为研究对象,采集和分析产业区中心河两边淹水环境下的水稻田、少用受污染河水灌溉的棉花田及不用受污染河水灌溉的蔬菜地样本,结果表明,产业区内土壤中铅和锌的含量明显高于产业区外。产业区内除水稻田土壤中铅的质量比超过评价参比值外,其他灌溉方式下土壤中铅和锌的质量比均未超过《土壤环境质量标准》(GB 15618-1995)中的二级标准(pH值>7)。统计分析表明,土壤中的重金属含量与废水灌溉方式有关,该产业区内土壤外源重金属来自钢丝绳产业的可能性很大。在不同的灌溉方式下,土壤剖面样品中的重金属含量随着土壤深度增加呈现降低的趋势,2010年和2011年的测定结果无显著差异。  相似文献   

7.
There is a growing concern over the potential accumulation of heavy metals in soils owing to rapid industrial and urban development and increasing reliance on agrochemicals in the last several decades. These metals can infiltrate through the soil thereby causing groundwater pollution. Surface soil samples (5 to 15 cm) collected from southeastern part of Ranga Reddy district were analyzed for 14 heavy metals (As, Ba, Co, Cr, Cu, Mo, Ni, Pb, Rb, Sr, V, Y, Zn and Zr) using Philips PW 2440 X-ray fluorescence spectrometer. Results for heavy and trace elements are reported for the first time in soils for this region. The contamination of the soils was assessed on the basis of enrichment factor (EF), geoaccumulation index (I (geo)), contamination factor and degree of contamination. The results reveal that variations in heavy element concentrations in the soil analyzed have both geogenic and anthropogenic contribution, due to the long period of constant human activities in the study area. The concentration of the metals Ba, Rb, Sr, V, Y and Zr were interpreted to be mainly inherited from parent materials (rocks) and the As, Co, Cr, Cu, Mo, Ni, Pb and Zn concentrations show contribution from geogenic and anthropogenic sources. The major element variations in soils are determined by the composition of the parent material predominantly involving granites.  相似文献   

8.
Total concentrations of Al, Ba, Cd, Co, Cr, Cu, Fe, Mn, Mo, Pb, Sr, Ti, V and Zn in the epiphytic lichen Parmelia sulcata and superficial soils from 60 remote sampling sites in Tuscany (central Italy) were determined to evaluate the contribution of soil to the elemental composition of the lichen. The results showed that in the Mediterranean environment, the trace element content of unwashed lichen samples is greatly affected by soil contamination. However, despite the strong correlations between the concentrations of lithogene elements such as Al, Fe and Ti in P. sulcata, lichen levels of these elements were not at all linearly correlated with their concentrations in the soil, suggesting that dust contamination is highly variable and probably dependent on local site characteristics. All methods evaluated to minimize soil contamination indicated Cu, Pb and Zn as elements of atmospheric origin. However, while levels of Pb were similar to those reported for background areas, moderate pollution by Cu and Zn, probably from fertilizers used in agriculture, was revealed. For elements such as Cd and Mo, identified as atmophile, some uncertainty exists due to the fact that they are essential for lichen metabolism and accumulate intracellularly in lichens; they may therefore occur in soluble form in the lichen thallus.  相似文献   

9.
某铀尾矿库周围农田土壤重金属污染潜在生态风险评价   总被引:6,自引:1,他引:5  
为能够定量评价铀尾矿库周围农田土壤重金属污染程度及其潜在生态危害性,采用Hakanson潜在生态风险指数法对土壤中重金属进行综合污染评价。结果表明,铀尾矿库周围部分农田土壤中重金属Cd、Ni、As、Cu、Hg、Zn含量存在积累和超标情况,尤以Cd的污染最严重,Ni、As次之;Pb、Cr含量能够满足标准限值要求。潜在生态风险评价结果显示,铀尾矿库周围农田土壤重金属潜在生态风险较高,主要潜在生态风险因子为Cd,其次是Hg、As,Cr、Pb、Ni、Cu、Zn并不构成潜在生态风险。铀尾矿库周围农田土壤中较高水平的Cd在构成环境污染的同时,也构成了较严重的生态危害,应加强对重金属Cd、Hg的生态风险防治。  相似文献   

10.
In this study, the relationship between some physico-chemical properties of soils and lead contamination in soil due to emission from industrial operations in Samsun province of Turkey was investigated. The extent of timely contamination was studied by comparing the obtained results with the results of the study conducted in the same region in 1998. An area of 225 km2 (15 km × 15 km), which was divided into 1000 × 1000 m grid squares (16 lines in the east and south directions), was selected within the industrial area. The total of 256 grid points was obtained and soil samples were collected from three depths (0–5, 5–15, and 15–30 cm) of each grid center in 2004. The total Pb concentrations of soil samples were determined as 65.84–527.04 μg g−1 at 0–5 cm in depth, 58.50 – 399.54 μg g−1 at 5–15 cm in depth, and 44.65–330.07 μg g−1 at 15–30 cm in depth. DTPA-extractable Pb concentrations of soils were found to be in the range of 1.52–9.03 μg g−1, 0.54–7.09 μg g−1, 0.19–6.13 μg g−1 at 0–5, 5–15, and 15–30 cm depths, respectively. There were significant relationships between both total or DTPA-extractable Pb concentrations and selected physico-chemical properties of soil. According to enrichment factor (EF) values calculated from the total Pb concentrations, 11.3% of the study area (225 km2) was enriched with Pb in high level, but 77% of the area was in significant enrichment level with Pb. The average total and DTPA-extractable Pb concentrations increased as 11 and 13%, respectively in comparison with the results of 1998.  相似文献   

11.
The Thriassio plain is located 25 km west of Athens city, the capital of Greece. Two major towns (Elefsina and Aspropyrgos), heavy industry plants, medium to large-scale manufacturing, logistics plants, and agriculture comprise the main land uses of the studied area. The aim of the present study was to measure the total and available concentrations of Cr, Zn, Ni, Pb, Co, Mn, Ba, Cu, and Fe in the top soils of the plain, and to asses soil contamination by these metals by using the geoaccumulation index (I geo), the enrichment factor (EF), and the availability ratio (AR) as soil pollution indexes. Soil samples were collected from 90 sampling sites, and aqua regia and DTPA extractions were carried out to determine total and available metal forms, respectively. Median total Cr, Zn, Ni, Pb, Co, Mn, Ba, Cu, and Fe concentrations were 78, 155, 81, 112, 24, 321, 834, 38, and 16?×?103 mg?kg?1, respectively. The available fractions showed much lower values with medians of 0.4, 5.6, 1.7, 6.9, 0.8, 5.7, 19.8, 2.1, and 2.9 mg?kg?1. Though median total metal concentrations are not considered as particularly high, the I geo and the EF values indicate moderate to heavy soil enrichment. For certain metals such as Cr, Ni, Cu, and Ba, the different distribution patterns between the EFs and the ARs suggest different origin of the total and the available metal forms. The evaluation of the EF and AR data sets for the soils of the two towns further supports the argument that the EFs can well demonstrate the long-term history of soil pollution and that the ARs can adequately portray the recent history of soil pollution.  相似文献   

12.
湖北省重点区域及周边表层土壤重金属污染现状及评价   总被引:1,自引:0,他引:1  
对湖北省内9类不同重点区域及周边表层土壤环境质量进行检测,测定重金属镉、汞、砷、铅、铬、铜、镍、锌含量水平,采用内梅罗污染指数法和Hakanson潜在生态风险指数法对检测结果进行评价。结果表明:9类不同重点区域及周边土壤环境质量整体良好,未受重金属污染的土壤监测点位比例为68.2%~92.6%,轻度污染的点位比例为5.8%~20.4%,中度污染为0.0%~8.6%,重度污染为0.0%~9.1%;污染企业周边、油田采矿区周边、固废处置场地周边、工业遗留遗弃场地及周边4类重点区域受重金属污染相对较严重,影响其土壤环境质量的重金属主要是镉、砷、铜、铅;9类不同重点区域周边土壤环境质量的潜在生态风险等级以轻微、中度为主,对应的监测点位比例分别为36.4%~80.5%、18.1%~47.7%,潜在生态风险等级为强度、很强、极强的监测点位比例总和为1.4%~15.9%,主要分布在受重金属污染严重的监测区域。  相似文献   

13.
乌鲁木齐市郊安宁渠区土壤重金属的污染调查   总被引:5,自引:0,他引:5  
胡慧玲 《干旱环境监测》2003,17(2):117-119,122
对乌鲁木齐产莱区安宁渠区的表层土壤及地表下40cm土壤中重金屑Cd、Hg、As、Pb、Cr进行了分析和测定,并对土壤中的重金属污染进行了环境质量评价。结果表明,安宁渠区土壤大部分为轻污染,但个别点已达重度污染,地表的污染较地表下40cm土壤为重。污染为外源性污染,与垃圾肥料的使用有关。  相似文献   

14.
The soils adjacent to an area of historical mining, ore processing and smelting activities reflects the historical background and a mixing of recent contamination sources. The main anthropogenic sources of metals can be connected with historical and recent mine wastes, direct atmospheric deposition from mining and smelting processes and dust particles originating from open tailings ponds. Contaminated agriculture and forest soil samples with mining and smelting related pollutants were collected at different distances from the source of emission in the Pb–Zn–Ag mining area near Olkusz, Upper Silesia to (a) compare the chemical speciation of metals in agriculture and forest soils situated at the same distance from the point source of pollution (paired sampling design), (b) to evaluate the relationship between the distance from the polluter and the retention of the metals in the soil, (c) to describe mineralogy transformation of anthropogenic soil particles in the soils, and (d) to assess the effect of deposited fly ash vs. dumped mining/smelting waste on the mobility and bioavailability of metals in the soil. Forest soils are much more affected with smelting processes than agriculture soils. However, agriculture soils suffer from the downward metal migration more than the forest soils. The maximum concentrations of Pb, Zn, and Cd were detected in a forest soil profile near the smelter and reached about 25 g kg − 1, 20 g kg − 1 and 200 mg kg − 1 for Pb, Zn and Cd, respectively. The metal pollutants from smelting processes are less stable under slightly alkaline soil pH then acidic due to the metal carbonates precipitation. Metal mobility ranges in the studied forest soils are as follows: Pb > Zn ≈ Cd for relatively circum-neutral soil pH (near the smelter), Cd > Zn > Pb for acidic soils (further from the smelter). Under relatively comparable pH conditions, the main soil properties influencing metal migration are total organic carbon and cation exchange capacity. The mobilization of Pb, Zn and Cd in soils depends on the persistence of the metal-containing particles in the atmosphere; the longer the time, the more abundant the stable forms. The dumped mining/smelting waste is less risk of easily mobilizable metal forms, however, downward metal migration especially due to the periodical leaching of the waste was observed.  相似文献   

15.
通过对四川省汉源县富泉乡万顺铅锌矿区土壤微生物区系及微生物活性的调查,结果表明,铅锌矿区土壤几种重金属含量明显高于临近非矿区土壤。该矿区土壤微生物区系组成和微生物活性显著不同于临近非矿区土壤,随着重金属含量的增加,土壤微生物数量、微生物多样性指数、微生物生物量碳以及纤维素分解强度均显著降低,但土壤基础呼吸却明显升高;土壤脲酶、碱性磷酸酶、多酚氧化酶对铅锌矿较为敏感,而蔗糖酶和过氧化氢酶受到的抑制作用不明显。  相似文献   

16.
广东某含铊硫酸冶炼堆渣场土壤中重金属的污染特征   总被引:3,自引:1,他引:2  
选取广东某硫酸厂工业堆渣周围土壤样品,重点研究了土壤剖面T1、cd、Pb、Zn四种重金属元素总量及形态分布特征.研究结果表明,该废渣在自然淋滤条件下已经对周围土壤产生了T1、Cd、Pb、Zn污染,并且T1、Pb、Cd较Zn污染严重.形态分析表明,堆渣场周围土壤中这些重金属主要是以残渣态和铁锰氧化物(氢氧化物)结合态存在.外围土壤受到的这些重金属污染及对环境的潜在危害大于废渣下伏土壤,其中在堆渣下伏土壤中主要以富集为主,而外围土壤中主要以迁移为主,且已经向土壤深处约30cm处进行了迁移.这些重金属污染物在表层土壤中未达到饱和状态,将继续在下伏土壤表层发生累积作用并且使横向土壤受污染的范围进一步扩大.  相似文献   

17.
This study was conducted to investigate the pollution load index, fraction distributions, and mobility of Pb, Cd, Cu, and Zn in garden and paddy soils collected from a Pb/Zn mine in Chenzhou City, China. The samples were analyzed using Leleyter and Probst’s sequential extraction procedures. Total metal concentrations including Pb, Cd, Cu, and Zn exceeded the maximum permissible limits for soils set by the Ministry of Environmental Protection of China, and the order of the pollution index was Cd > Zn > Pb > Cu, indicating that the soils from both sites seriously suffered from heavy metal pollution, especially Cd. The sums of metal fractions were in agreement with the total contents of heavy metals. However, there were significant differences in fraction distributions of heavy metals in garden and paddy soils. The residual fractions of heavy metals were the predominant form with 43.0% for Pb, 32.3% for Cd, 33.5% for Cu, and 44.2% for Zn in garden soil, while 51.6% for Pb, 40.4% for Cd, 40.3% for Cu, and 40.9% for Zn in paddy soil. Furthermore, the proportions of water-soluble and exchangeable fractions extracted by the selected analytical methods were the lowest among all fractions. On the basis of the speciation of heavy metals, the mobility factor values of heavy metals have the following order: Cd (25.2–19.8%) > Cu (22.6–6.3%) > Zn (9.6–6.0%) > Pb (6.7–2.5%) in both contaminated soils.  相似文献   

18.
An oil spill polluted site at Ogbodo-Isiokpo in Ikwere Local Government Area of Rivers State in southern Nigeria, was identified for study following three successive reconnaissance surveys of oil fields in the Agbada west plain of Eastern Niger Delta. A sampling area of 200 m × 200 m was delimited at the oil spill impacted site using the grid technique and soils were collected at surface (0–15 cm) and subsurface (15–30 cm) depths from three replicate quadrats. A geographically similar, unaffected area, located 50 m adjacent to the polluted site, was chosen as a control (reference) site. Total extractable hydrocarbon contents of the polluted soils ranged from 3.02–4.54 and 1.60–4.20 mg/kg (no overlap in standard errors) at surface and subsurface depths respectively. The concentrations of two “diagnostic” trace heavy metals, nickel (Ni) and vanadium (V), which are normal constituents of crude oil, were also determined in the soils by atomic absorption spectrophotometric method after pre-extraction of cations with dithionite–citrate carbonate. Ni varied from 0.15 to 1.65 mg/kg in the polluted plots and from 0.18 to 0.82 mg/kg in the unpolluted plots; vanadium varied from 0.19 to 0.70 mg/kg in the polluted plots and from 0.14 to 0.38 mg/kg in the unpolluted plots. Ni and V were more enhanced (p < 0.05) in the oil-polluted soils, especially at subsurface depth. Whilst the oil spillage could be said to be indirectly responsible for the enhanced concentrations of nickel and vanadium via the injection and availability of the petroleum hydrocarbons that might have increased the activities of biodegradation on site, the physico-chemical properties of the soils and inherent mobility of metals, as well as the intense rainfall and flooding that characterized the period of study, may have also contributed, at least in part, to these enhanced concentrations. Such levels of Ni and V may result to enhanced absorption by plants, which may bring about possible bioaccumulation in such plants and the animals that depend on them for survival and all of these may lead to toxic reactions along the food chain.  相似文献   

19.
The use of a combination of electrokinetic remediation and phytoremediation to decontaminate two metal-polluted soils has been demonstrated in laboratory-scale reactors. One soil was heavily contaminated with copper, the other with cadmium and arsenic (2500 g g-1 Cu; 300-400 g g-1 Cd and 230 g g-1 As, respectively). Test reactors with twoseparated chambers, each with a capacity of 5.25 kg soil, wereconstructed, then the respective chambers were filled with eithera mixture of the polluted soil and a control topsoil (75:25) ortopsoil alone. Reactors were sown with perennial ryegrass (Lolium perenne cv Elka) and a constant voltage of 30 V was applied continually across the soils in each reactor. Soil sampling took place at the start and the end of the test run, whilst plant foliage was sampled after approximately 3 weeks (both reactors) 6 weeks (Cd soil reactor only) and at the conclusion of each test run (98 days Cu soil, 80 days Cd soil). Soil and plant metal concentrations were measured, together withsoil pH. Results showed that in both soils there was a significant re-distribution of metals from anode to cathode in the test reactors, coupled with an enhancement of plant Cu uptakein the cathode region for the Cu soil. Patterns of plant Cd uptake were less clear cut and were not as clearly related to theredistribution of Cd measured in the soil. There was significant acidification of soil at the anode in each test reactor, but soilpH in other parts of the reactor changed little during the courseof the experiment. Plant growth was affected at the anode, but was not affected in other parts of the reactor. There was no visual evidence of metal toxicity in the ryegrass in either polluted soil. Some effects on soil fungi were apparent, with a stimulation of Fusarium infection of ryegrass in the cathode region of all reactors and the appearance of sporophoresof Coprinus in the same location. It is concluded that the combination of the two techniques represents a very promising approach to the decontamination of metal polluted soils that nowrequires validation in field conditions.  相似文献   

20.
Heavy Metal Pollution of Surface Soil in the Thrace Region, Turkey   总被引:1,自引:0,他引:1  
Abstact Samples of surface soil were collected at 73 sites in the Thrace region, northwest part of Turkey. Two complementary analytical techniques, epithermal neutron activation analysis (ENAA) and atomic absorption spectrometry (AAS) with flame and graphite furnace atomization were used to determine 35 elements in the soil samples. Concentrations of As, Cd, Co, Cu, Mn, Ni, Pb and Zn were determined using AAS and GF AAS, and ENAA was used for the remaining 27 elements. Results for As, Ba, Br, Ca, Cd, Ce, Co, Cr, Cs, Cu Eu, Fe, Hf, I, In, K, La, Mn, Mo, Na, Nd, Ni, Pb, Rb, Sb, Sc, Sm, Sr, Ta, Tb, Th, Ti, U, V and Zn are reported for the first time for soils from this region. The results show that concentrations of most elements were little affected by the industrial and other anthropogenic activities performed in region. Except for distinctly higher levels of Pb, Cu, Cd and Zn in Istanbul district than the median values for the Thrace region, the observed distributions seem to be mainly associated with lithogenic variations. Spatial distributions of As, Cd, Cr, Cu, Ni, Pb and Zn were plotted in relation to the concentration values in soil using Geographic Information System (GIS) technology  相似文献   

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