首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 46 毫秒
1.
Atmospheric polycyclic aromatic hydrocarbons (PAHs) were determined in particulate matter (PM10) collected in a suburban area with industrial and vehicular emissions in the Metropolitan Area of Rio de Janeiro City (Brazil). A total of 22 samples were collected between March and August 2005 by means of a high volume PM10 sampler. The particulate matter contained in the filters was extracted ultrasonically with dichloromethane. The extracts were later analyzed by gas chromatography coupled to a mass spectrometer (GC/MS). The individual concentrations of PAHs ranged between the detection limit and 0.386 ng m?3. The PAHs concentrations observed in this study were towards the lowest end of the range of values reported for other European locations and also lower than values obtained for South America. PAHs concentrations and molecular ratios showed that light cars seem to be the main contributors to PM10 emissions, but diesel vehicles are clearly minor emission sources and industrial contributions should not be disregarded until more data are obtained.  相似文献   

2.
The Marais Vernier is the largest freshwater wetland in the Seine Estuary in northern France. It is in a heavily urbanized and industrialized region and could be affected by atmospheric deposition and by fluvial input of contaminants in water diverted from the Seine River. To evaluate contaminant histories in the wetland and the region, sediment cores were collected from two open-water ponds in the Marais Vernier: the Grand-Mare, which was connected to the Seine by a canal from 1950 to 1996, and the Petite Mare, which has a small rural watershed. Diversions from the Seine to the Grand-Mare increased sedimentation rates but mostly resulted in low contaminant concentrations and loading rates, indicating that the sediment from the Seine was predominantly brought upstream by tidal currents from the estuary and was not from the watershed. Atmospheric sources of metals dominate inputs to the Petite Mare; however, runoff of metals from vehicle-related sources in the watershed might contribute to the upward trends in concentrations of Cr, Cu, and Zn. Estimates of atmospheric deposition using the Petite Mare core are consistent with measured deposition in the region and are mixed (similar for Hg and Pb; larger for Cd, Cu, and Zn) compared with deposition estimated from sediment cores in the northeastern United States. A local source of PAHs in the watershed of the Petite Mare is indicated by higher concentrations, higher accumulation rates, and a different, more petrogenic, PAH assemblage than in the Grand-Mare. The study illustrates how diverse sources and transport pathways can affect wetlands in industrial regions and can be evaluated using sediment cores from the wetland ponds.  相似文献   

3.

Purpose

The purpose of this study was to elucidate historical trends, spatial variations, and the sources of polycyclic aromatic hydrocarbons (PAHs) pollution in several Japanese lakes.

Materials and methods

The vertical distributions of PAHs in the core samples of sediments taken at several points in lakes Kasumigaura, Suwa, Kizaki, and Shinji were determined using a gas chromatograph equipped with a mass selective detector and combined with chronological information and the physical/elemental properties of the sediment.

Results and discussion

Seventeen related compounds (congeners) typically had concentration peaks at sediment depths corresponding to the 1960s to 1970s. In Lake Shinji and one bay of Lake Kasumigaura, there was a tendency for PAH concentrations to increase downstream; in contrast, another bay of Lake Kasumigaura showed the reverse trend. During big flood events, the fluxes of PAHs increased due to large inputs of particulate matter, although PAH concentrations were reduced. For the four study lakes and other similar lakes, PAH concentrations of surface sediments were approximately proportional to population densities in the respective watersheds, while the total input of PAHs to the lakes were correlated with their population and watershed area. The source apportionment analysis using isomer ratios for the congener profiles indicated that the principal sources of the PAHs in the lake sediments were gasoline and/or diesel engine exhausts and biomass burning.

Conclusions

The observed concentration peaks showed a deterioration of the chemical quality of atmospheric conditions around 1960?C1970 and a recent tendency for their amelioration. Between-lake differences suggest that the influence of human activity in the watersheds influences sediment PAH concentrations. The PAH sources were identified to be of pyrogenic origin.  相似文献   

4.
Atmospheric bulk deposition was collected on a monthly basis in the Lake Michigan basin from September 1975 through December 1976 to determine the atmospheric loading of trace elements to Lake Michigan. The sampling network consisted of bulk collectors located at 21 locations in the northern and southern basin. Atmospheric loading rates to Lake Michigan were estimated as (in units of 105 kg yr?1): Al-50; Fe-28; Mn-6.4; Zn-11; Cu-1.2; Pb-6.4; Cd-0.11; Co- <0.25; Ca-798; Mg-155; Na-110; K-64. Atmospheric deposition of all elements measured was greater in the southern basin than in the northern basin as a result of intense urban/industrial activity in the former. The percentage of total atmospheric deposition falling in the southern basin was: Fe-74%, Al-71%; Mn-75%; Zn-67%; Cu-62%; Pb-78%; Cd-74%; Co- ti 56%; Ca-79%; Mg-62%; Na-65%; K-61 %. Atmospheric loading rates reported are in general agreement with estimates made by others from emission inventories and aerosol concentrations. Atmospheric loadings were estimated to represent 10% or more of the total loadings to Lake Michigan from tributary and erosion sources for the trace elements Mn, Zn, Cu, Cd and Pb. Also, atmospheric deposition may account for recent accumulations of Zn, Cu, Cd, Pb and Co in southern Lake Michigan surficial sediments. The atmospheric Ph flux to southern Lake Michigan was estimated as ～1.7 μg sm?2 yr?1 for 1975–1976 which compares favorably with the 1972 anthropogenic Pb flux of 1.3 μg cm?2 yr?1 (total ? ～1.5 μg cm?2 yr?1) as determined from Pb-210 dating (Edgington and Robbins, 1976). The geographical distribution of trace element loading implicates the southern periphery of Lake Michigan as the principal emission source area.  相似文献   

5.
Polycyclic aromatic hydrocarbons (PAHs); their derivatives nitro, and methyl-PAHs; n-alkanes; and organic acids were investigated in the aerosol samples collected during two field campaigns conducted at three sampling stations in an industrialized city in southern Italy. The main sources affecting the atmosphere and its toxicity were investigated by means of the diagnostic ratios of: specific particulate-phase PAHs, marker compounds among nitro-PAHs, alkanes, and acids, the dominant wind direction, daily and seasonal abundance of carcinogenic organic substances. The potential importance of the non-regulated pollutants to assess the air quality was confirmed; in fact the carcinogenic organic compounds showed to have scarce correlation with particulate matter (PM) concentration. An exceptionally high variability of toxic compounds at a daily scale was due to meteorological condition causing periods of extremely high pollution levels.  相似文献   

6.
Aim and Background  Little data are available on the levels of polycyclic aromatic hydrocarbons (PAHs) in the sediments of the Mediterranean Sea Coast of Egypt in general and the Alexandria coastal zone in particular. It was therefore deemed necessary to set up a monitoring programme to determine the current concentrations of PAHs in bottom sediments, and to identify any area where high concentrations of these potential hazardous contaminants were present in the Western Harbour of Alexandria. Methods  The composition, distribution and the source of PAHs in surficial sediments of the harbour were investigated. To document the spatial PAH input, surficial sediment samples from 23 locations throughout the harbour were analysed. as]Results and Discussion The total PAH load determined in the surficial sediment samples ranged from 8 to 131150 ng g1 dry wt, generally with most of the samples having total concentrations of PAHs greater than 5000 ng g1 dry weight. The highest concentration of total PAHs was recorded in sediments of the inner harbour. Ratio values of specific compounds such as phenanthrene to anthracene, fluoranthrene to pyrene, methyl-phen-anthrene to phenanthrene, methyl-dibenzothiophenes to dibenzothiophenes, alkylated to non-alkylated and high molecular weight to low molecular weight PAH, were calculated to evaluate the possible source of PAH contamination in the harbour sediments. Conclusions  Two main sources of PAH in the study area have been found: pyrolytic and petrogenic. Interferences of rather petrogenic and pyrolytic PAH contaminations were noticed for most samples. The dominant sources of PAH appear to be the combustion processes through run-off, industrial and sewage discharges, and atmospheric input. The concentrations of PAHs were generally above levels expected to cause adverse biological effects. Recommendations and outlook  Information from this study and any other relevant studies should be useful in designing future strategies for environmental protection and management of the harbour.  相似文献   

7.
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous toxic organic pollutants in the natural environment that are strongly associated with socioeconomic activities. Exploring the distribution, sources, and ecological toxicity of PAHs is essential to abate their pollution and biological risks. The 16 priority PAHs in different lakeside city estuarine sediments in the northern Taihu Lake in China were determined using gas chromatography-mass spectrometry. Results showed that total concentrations...  相似文献   

8.
怠速是非道路用柴油机重要的运行工况之一。为了深入探究大气压力对小型农用柴油机怠速工况下燃烧与排放性能的影响,利用大气压力模拟装置,研究了满足非道路国III排放标准的小型农用柴油机在怠速工况下燃烧特性与排放性能随大气压力(80、90、100 kPa)的变化规律。试验结果表明:在怠速工况下,小型农用柴油机匹配的涡轮增压器不起作用,并且在高原地区涡轮增压系统不具备自补偿能力;最高缸内压力、压力升高率峰值以及放热率峰值均随着大气压力的升高而升高,大气压力每升高10 kPa,上述燃烧参数分别平均升高13.33%、37.24%以及6.76%;而最高缸内燃烧温度随着大气压力的升高而降低,大气压力每升高10 kPa,平均降低11.18%;大气压力对CO排放与HC排放影响较大,大气压力每升高10 kPa,CO排放与HC排放分别平均降低47.47%与55.77%;大气压力对NO_x排放与烟度的影响相对较小,大气压力每升高10 kPa,NO_x排放平均升高18.93%,而烟度平均降低11.90%。该研究可为高原地区小型农用柴油机怠速工况的排放控制提供参考依据。  相似文献   

9.
A set of 72?PM10 samples from low-polluted urban and rural locations belonging to the regional air monitoring network of Extremadura (Spain) were collected in a 1?year sampling period. Sample pre-treatment and analytical determination by gas chromatography?Cion trap mass spectrometry were optimised and validated for the analysis of the priority 16 US Environmental Protection Agency polycyclic aromatic hydrocarbons (PAHs). The influence of meteorological conditions (temperature, relative humidity and solar radiation) and other atmospheric pollutants (O3, NO2, SO2, PM10) has been covered in detail and Pearson correlation test were used for this purpose. Spatial distribution of particulate PAHs was evaluated and the comparison with other European sites was also established. Possible emission sources were identified and assigned by using molecular diagnostic criteria.  相似文献   

10.
东亚季风与城市活动影响下南京市大气沉降多元特征研究   总被引：2，自引：0，他引：2  
Atmospheric deposition, a major pathway of metals entering into soils, plays an important role in soil environment, especially in urban regions where a large amount of pollutants are emitted into atmosphere through various sources. In order to understand the characteristics of atmospheric deposition in urban area and its relation with natural and anthropogenic sources, a three-year study of atmospheric deposition at three typical sites, industrial zone (IN), urban residential area (RZ) and suburban forested scenic area (FA), was carried out in Nanjing, a metropolitan city in eastern China from 2005 to 2007. The bulk deposition rate and element composition of atmospheric deposition varied spatio-temporally in the urban zones of Nanjing. The concentrations of Cu, Zn, Pb and Ca in the atmospheric deposits were strongly enriched in the whole Nanjing region; however, anthropogenic pollutants in atmospheric deposits were diluted by the input of external mineral dust transported from northwestern China. Source apportionment through principal component analysis (PCA) showed that the background atmospheric deposition at the FA site was the combination of external aerosol and local emission sources. The input of long-range transported Asian dust had an important influence on the urban background deposition, especially in spring when the continental dust from the northwestern China prevailed. Marine aerosol source was observed in summer and autumn, the seasons dominated by summer monsoon in Nanjing. In contrast, the contribution of local anthropogenic emission source was constant regardless of seasons. At the RZ and IN sites, the atmospheric deposition was more significantly affected by the nearby human activities than at the FA site. In addition, different urban activities and both the winter and summer Asian monsoons had substantial impacts on the characteristics of dust deposition in urban Nanjing.  相似文献   

11.
Atmospheric deposition and above-ground cycling of sulfur (S) were evaluated in adjacent deciduous and coniferous forests at the Panola Mountain Research Watershed (PMRW), Georgia, U.S.A. Total atmospheric S deposition (wet plus dry) was 12.9 and 12.7 kg ha-1 yr-1 for the deciduous and coniferous forests, respectively, from October 1987 through November 1989. Dry deposition contributes more than 40% to the total atmospheric S deposition, and SO2 is the major source (～55%) of total dry S deposition. Dry deposition to these canopies is similar to regional estimates suggesting that 60-km proximity to emission sources does not noticeably impact dry deposition at PMRW. Below-canopy S fluxes (throughfall plus stemflow) in each forest are 37% higher annually in the deciduous forest than in the coniferous forest. An excess in below-canopy S flux in the deciduous forest is attributed to leaching and higher dry deposition than in the coniferous forest. Total S deposition to the forest floor by throughfall, stemflow and litterfall was 2.4 and 2.8 times higher in the deciduous and coniferous forests, respectively, than annual S growth requirement for foliage and wood. Although S deposition exceeds growth requirement, more than 95% of the total atmospheric S deposition was retained by the watershed in 1988 and 1989. The S retention at PMRW is primarily due to SO4 2- adsorption by iron oxides and hydroxides in watershed soils. The S content in white oak and loblolly pine boles have increased more than 200% in the last 20 yr, possibly reflecting increases in emissions.  相似文献   

12.
Ustica is an island relatively far from continental, industrial and urban settlements and it has been designated as a marine protected area with the aim of preserving the natural diversity of flora and fauna of the surrounding sea. In such an environment, the assessment of the levels and origin of persistent organic pollutants such as polycyclic aromatic hydrocarbons (PAHs) can shed light on the mechanisms and effects of pollutant long-distance transport in the western Mediterranean Sea. PAHs concentrations resulted relatively low when compared with those of other coastal areas of the Mediterranean Sea. The low values of the ratio between low- and high-molecular-weight (LMW and HMW, respectively) PAHs and the fluoranthene and pyrene ratios underlined a pyrolytic origin of these contaminants. The prevalence of HMW-PAHs, however, may also be due to the effect of LMW-PAH preferential degradation during transport and burial into sediments. On the other hand, petrogenic sources prevailed in the past. Whilst PAHs concentrations showed a recent increase, especially at the site close to the port, the estimated sedimentary fluxes of PAHs ranged from 0.5 to 25 μg m?2 year?1.  相似文献   

13.
Surface and core sediments from Lake Maryut, Egypt, one of the most polluted lakes in Egypt, were analyzed for polycyclic aromatic hydrocarbons (PAHs) using gas chromatography?Cmass spectrometry. This investigation represents the first extensive study of the distribution and sources of PAHs in sediments from Lake Maryut. The total PAHs concentrations (sum of 39 PAH compounds) in surface sediments varied greatly depending on the sampling location and ranged from 106 to 57,800 ng/g dry weight with a mean concentration of 6,950 ng/g. The most polluted areas are distributed in areas which are mainly influenced by municipal sewage and industrial effluent discharges, suggesting a direct influence of these sources on the pollutant distribution patterns. PAH concentrations were one to two orders of magnitude higher in comparison with those reported for riverine/estuaries systems around the world. Molecular indices, such as pyrogenic index (PI), methylphenanthrenes to phenanthrene ratio, HMWPAH/LMWPAH, A-PAHs/P-PAHs, FL/FL?+?PY, BaP/BaP?+?C, IP/IP?+?BgP, and Per/??(penta-aromatics) were calculated to evaluate different hydrocarbon origins and their relative importance. In general, sediments from the main basin and northwest basin of Lake Maryut showed the highest PAH concentrations with petrogenic signatures, indicating major sources of petrogenic PAHs in the city. On the other hand, lower levels of PAHs with a pyrogenic signature were widely recorded in areas that are distant from anthropogenic sources. At other locations, both petrogenic and pyrogenic inputs were significant. The concentrations of perylene relative to the penta-aromatic isomers are dominant especially in locations associated with terrestrial inputs and in the deepest core sediments, indicating diagenetic origin for the presence of perylene. Temporal trends of PAH concentrations in both cores sediments were influenced by input pathways and followed the economic development and the environmental policies of the Egyptian Government in the last 15 years. Finally, PAH levels in sediments were compared with Sediments Quality Guidelines (effects range median?Ceffects range low) for evaluation probable toxic effects on organism. Results suggest an ecotoxicological risk for benthic organisms mainly in the main basin area, where high concentrations of PAHs were found in sediments influenced by anthropogenic activities.  相似文献   

14.
Concentrations of mercury (Hg) were measured in six dated cores from four lakes in western Whatcom County, Washington, USA, that were at various bearings from a chlor-alkali plant, two municipal waste incinerators and a municipal sewage sludge incinerator. The importance of atmospheric emissions of Hg from these local municipal and industrial sources was evaluating by comparing the temporal trends in sedimentation of the lake cores with the emission history of each Hg species and by examining the geographical distribution of Hg sedimentation in relation to the region’s primary wind pattern. Local municipal and industrial sources of atmospheric Hg were not responsible for the majority of the Hg in the upper layer of sediments of Whatcom County lakes because of (1) the significant enrichment of Hg in lake sediments prior to emissions of local industrial and municipal sources in 1964, (2) smaller increases in Hg concentrations occurred after 1964, (3) the similarity of maximum enrichments found in Whatcom County lakes to those in rural lakes around the world, (4) the inconsistency of the temporal trends in Hg sedimentation with the local emission history, and (5) the inconsistency of the geographic trends in Hg sedimentation with estimated deposition. Maximum enrichment ratios of Hg in lake sediments between 2 and 3 that are similar to rural areas in Alaska, Minnesota, and New England suggest that global sources of Hg were primarily responsible for increases of Hg in Whatcom County lakes beginning about 1900.  相似文献   

15.
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants in the urban atmosphere. In particular, atmospheric pollution has increasingly become severe in China due to its rapid urbanization and industrialization. In recent years, a few studies have presented information about POPs (such as PAHs, PCBs, OCPs) in aerosols at a molecular level in a limited number of cities such as Beijing, Qingdao and Guangzhou, as well as Hong Kong. Whereas, these cities are located in northern and southern China, respectively, where characteristics of atmospheric pollution might be different from those in the eastern cities, such as Shanghai. Atmospheric particle pollution is a persistent problem in Shanghai, a typical metropolis of China, which has several huge industrial regions. In order to gain a comprehensive understanding of the present state, properties and sources of PAHs pollution in Shanghai, PM10 samples were collected at Coal-Fired Power Plant (CFP), Chlor-Alkali Chemical factory (CAC) and Coking and Chemical factory (CCF) in an industrial area, during the period, November 2004–September 2005. The concentrations of 16 PAHs were analyzed using the HPLC with UV visible detector. The results showed that the mean value of total PAHs in the industrial area was 64.85 ng m?3; 3-ring PAHs were found at low levels, while 4-, 5- and 6-ring PAHs were found at high levels. The levels of BaP were 3.07 and 7.16 ng m?3 at Chlor-Alkali Chemistry Factory and Coking and Chemistry Factory sites, respectively. PAHs levels exhibited distinct seasonal variation, with the highest level in autumn and the lowest in summer. The major source of PAHs at the industrial area was fossil fuel combustion, coal-burning, industrial furnaces including others. There was a very significant correlation of PAHs levels between CCF and CAC (R 2?=?0.91). The average concentration of BaP in the industrial area during the sampling period was 5.95 ng m?3. It could be concluded the local population appears to be exposed to significantly high cancer risk (exceeding 2 ng m?3 in autumn and winter) as compared to the population of other areas.  相似文献   

16.
以南湖水体中的水、表层沉积物、生物膜和悬浮物为研究对象,对美国EPA规定的16种优控PAHs中13种PAHs的分布与富集特征进行了研究。结果表明,表层沉积物中检出12种PAHs,生物膜和水相中均检出11种PAHs,而悬浮物中只检出7种PAHs;生物膜和悬浮物富集PAHs的能力相近,比表层沉积物的富集能力大一个数量级;相关分析表明,生物膜和悬浮物富集PAHs的能力归因于其有机质（TOC）的含量高于表层沉积物中有机质的含量。根据菲/蒽比值和PAHs环数相对丰度对南湖表层沉积物中PAHs的来源进行了分析,发现南湖沉积物中的PAHs主要来自于化石燃料燃烧释放的污染。  相似文献   

17.
From 1990 to 1994, a total of 21 sediment cores and 37 grab sediment samples were collected from the Milwaukee Harbor Estuary. Each sediment core was sectioned and dated using 210Pb and137 Cs radioisotope techniques. A total of 305 samples were analyzed for sixteen polycyclic aromatic compounds (PAHs). Grain size distribution, porosity, and total organic carbon content as measured by loss on ignition were also determined. The results provide a historical overview of the impact of industrialization in the Milwaukee area. Although highly variable, the concentration profile of PAHs show, in general, peaks in the 1950's through 1980's. The PAH concentrations have declined since then for most sediment cores. The current levels of total PAHs in most surface sediment samples range from 25 to 200 ppm. A few cores, some of which were collected in 1994, have an elevated PAH concentration at the surface. Toxicity of the surface sediments was evaluated by comparing with the benchmark values developed by the United States National Oceanic and Atmospheric Administration (NOAA). The most heavily contaminated area was found in the Kinnickinnic River between the Becher Street Bridge and the Wisconsin Wrecking Company Wharf. The highest total PAH concentration determined from seven vibra cores collected in this area ranges from 380 to 1000 ppm. The former Wisconsin Solvay Coke Company may have been a major point source of PAHs until the 1970's. Highway traffic and various industrial discharges also contribute to the sediment PAHs in this area.  相似文献   

18.
采集南京地区不同有机污染风险区农田表层土壤,用超快速液相色谱仪检测样品中15种EPA优控的多环芳烃(PAHs)含量。结果表明,被检农田土壤多环芳烃总量分布于306.0~1251.3μg kg~(-1)之间,均值682.0μg kg~(-1),四环以上高环多环芳烃占较大比例(80%)。根据欧洲土壤质量标准,所检土壤样本已达污染水平。不同风险污染区农田土壤PAHs的含量由高至低为:钢铁工业区、有机垃圾处理区、化工工业区及炼油工业区。钢铁工业区附近主要的污染物为荧蒽、芘、屈和苯并[a]蒽,分别占到污染物总量的16%、13%、10%和10%。采用荧蒽/(荧蒽+芘)与茚并[1,2,3-cd]芘/(茚并[1,2,3-cd]芘+苯并[g,h,i]苝)比值对各地污染物来源进行分析,结果发现调查区域的PAHs污染物以燃烧源为主,生物质燃料为主要污染物,部分地区同时有石油燃烧污染。  相似文献   

19.
Polycyclic aromatic hydrocarbons (PAHs) are considered to be atmospheric pollutants and well-known human carcinogens. This study analyzes the pollution scenarios of PAHs in the aerosol of Higashi Hiroshima, Japan. We examined the characteristics, the influences of meteorological conditions, the distribution and seasonal variation of PAHs in aerosol samples collected from June 2000 to May 2001. The concentration of PAHs in the aerosol of Higashi Hiroshima was ranging from 11.8 to 157.5 μg/g with a mean concentration of 63.4 μg/g. Results showed that there is positive correlation between aerosol PAH concentrations and ambient temperature but a relatively little correlation with solar radiation. Seasonal variation was observed with a higher concentration during winter and lower concentration during summer. Apart from that, principal component analysis and molecular diagnostic ratios were also used to characterize and identify possible PAHs emission sources. Results obtained strongly suggested that vehicular emissions appeared to be the major source of aerosol PAHs in this study although other sources do have some degree of influence.  相似文献   

20.
太原小店污灌区农田土壤多环芳烃的污染特征及其来源   总被引：1，自引：0，他引：1  
赵颖  张丽 《水土保持通报》2017,37(4):99-105
[目的]对太原小店污灌区农田土壤多环芳烃(PAHs)的污染特征及来源进行分析,为该区农田土壤环境质量评价及土壤污染防治对策的制定提供科学依据。[方法]采集太原小店污灌区15个表层土壤样品,利用GC/MS分析16种US EPA优控多环芳烃(PAHs)的含量,并对其来源和生态风险进行探讨。[结果]所有样品的16种PAHs均被检出,其检出率为100%。研究区农田土壤中总PAHs的浓度为0.315~7.661μg/g,平均值为3.568μg/g。在组成上,2,3环含量约占总量的64.2%,4环含量约占总量的14.2%,5,6环含量约占总量的21.6%,低环和中环PAHs含量所占的比例较高。根据特征比值法及调查结果判定,农田土壤中PAHs污染来源一方面与灌溉水质及灌溉历史有很大的关系,另一方面,主要通过燃煤或化石燃料产生的PAHs在大气干湿沉降和风力输送作用下进入到土壤环境中。[结论]与国内外其他地区的相关研究比较,小店污灌区农田土壤PAHs含量处于中高等污染水平。依据Maliszewska-Kordybach建议的分级标准评价,该区域所有采样点PAHs总量均超标;但基于我国《土壤环境质量标准(征求意见稿)(GB15618-2008)》提出的16种多PAHs污染物总量的农业用地标准值,该区域均未超出此标准。  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号