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1.
In order to investigate the chemical characteristics of atmospheric aerosols in a regional background site, PM2.5 and PM10 were collected at Mount Gongga Station once a week in 2006. The concentrations of fifteen elements including Na, Mg, Al, K, Ca, V, Fe, Ni, Cu, Zn, As, Ag, Ba, Tl, and Pb were detected by Inductively Coupled Plasma Mass Spectrometer (ICP-MS). The results showed that Na, Mg, Al, K, Ca, Fe were the major components of elements detected in PM2.5 and PM10, occupied 89.5% and 91.3% of all the elements. Crustal enrichment factor (EF) calculation indicated that several anthropogenic heavy metals (Ni, Cu, Zn, As, Ag, Tl, Pb) were transported long distances atmospherically. The concentrations of all elements (except Na) measured in PM2.5 and PM10 in spring and winter were higher than those in summer and autumn. The backward air mass trajectory analysis suggests that northeast India may be the source region of those pollutants.  相似文献   

2.
Simultaneous measurements on physical, chemical and optical properties of aerosols over a tropical semi-arid location, Agra in north India, were undertaken during December 2004. The average concentration of total suspended particulates (TSP) increased by about 1.4 times during intense foggy/hazy days. Concentrations of SO4 2−, NO3 −, NH4 + and Black Carbon (BC) aerosols increased by 4, 2, 3.5 and 1.7 times, respectively during that period. Aerosols were acidic during intense foggy/hazy days but the fog water showed alkaline nature, mainly due to the neutralizing capacity of NH4 aerosols. Trajectory analyses showed that air masses were predominantly from NW direction, which might be responsible for transport of BC from distant and surrounding local sources. Diurnal variation of BC on all days showed a morning and an evening peak that were related to domestic cooking and vehicular emissions, apart from boundary layer changes. OPAC (Optical properties of aerosols and clouds) model was used to compute the optical properties of aerosols. Both OPAC-derived and observed aerosol optical depth (AOD) values showed spectral variation with high loadings in the short wavelengths (<1 μm). AOD value at 0.5 μm wavelength was significantly high during intense foggy/hazy days (1.22) than during clear sky or less foggy/hazy days (0.63). OPAC-derived Single scattering albedo (SSA) was 0.84 during the observational period, indicating significant contribution of absorbing aerosols. However, the BC mass fraction to TSP increased by only 1% during intense foggy/hazy days and thereby did not show any impact on SSA during that period. A large increase was observed in the shortwave (SW) atmospheric (ATM) forcing during intense foggy/hazy days (+75.8 W/m2) than that during clear sky or less foggy/hazy days (+38 W/m2), mainly due to increase in absorbing aerosols. Whereas SW forcing at surface (SUF) increased from −40 W/m2 during clear sky or less foggy/hazy days to −76 W/m2 during intense foggy/hazy days, mainly due to the scattering aerosols like SO4 2-.  相似文献   

3.
The data on deposition density of Ag, Al, As, B, Ba, Be, Bi, Br, Ca, Cd, Co, Cr, Cs, Cu, Fe, I, K, Li, Mg, Mn, Mo, Na, Ni, P, Pb, Rb, S, Sb, Se, Si, Sn, Sr, Th, Tl, U, V, Zn, Cl?, F?, NO 3 ? , and SO 4 2? in atmospheric precipitation were derived at six stations in the Republic of Karelia. The structure and space-time distribution of five sets (factors) of chemical components of the first order and two factors of the second order are revealed with the help of hierarchical factor analysis. Factor analysis of the second order demonstrated that atmospheric precipitation chemistry at all stations considered differs greatly in the winter and summer, forming two independent sets of components. The first-order factors revealed chemical indicators characterizing specific features of the atmospheric precipitation chemistry in the Karelian regions studied.  相似文献   

4.
Over a period of one year, the moss Scleropodium purum was sampled every two weeks in a French rural area to determine the levels of Li, Na, Al, Si, P, Ca, V, Mn, Fe, Zn, Ba, Hg, and Pb. The element distribution in the moss shoot was studied throughout the year. An apical bioconcentration was discovered for Na, P, Ca, Mn, and Zn, whereas higher levels were found in the basal fraction for Li, Al, Si, V, Fe, Ba, Hg, and Pb. A significant variation of element concentrations was observed during the sampling period. In the apical part Li, Al, Si, V, Fe, Ba, and Hg show maximum levels in the summer and minimum in the autumn. The same pattern was found with Ca and Mn in the whole plant, whereas Na showed opposite fluctuations.  相似文献   

5.
A continuous measurement of number size distributions and chemical composition of aerosol particles was conducted in Beijing in a dust storm event during 21-26 March 2001. The number concentration of coarse particles （ 〉2μm） increased more significantly than fine particles （ 〈2μm） during the dust storm due to dust weather, while the anthropogenic aerosols collected during the non-dust-storm period tended to be associated with fine particles. Elemental compositions were analyzed by using proton-induced X-ray emission （PIXE）. The results show that 20 elements in the dust storm were much higher than in the non-dust-storm period. The calculated soil dust concentration during the dust storm was, on average, 251.8μg m^-3, while it was only 52.1μg m^-3 on non-dust-storm days. The enrichment factors for Mg, A1, P, K, Ca, Ti, Mn, Fe, C1, Cu, Pb, and Zn show small variations between the dust storm and the non-dust-storm period, while those for Ca, Ni and Cr in the dust storm were much lower than those in the non-dust-storm period due to significant local emission sources. A high concentration and enrichment factor for S were observed during the dust storm, which implies that the dust particles were contaminated by aerosol particles from anthropogenic emissions during the long-range transport. A statistical analysis shows that the elemental composition of particles collected during the dust storm in Beijing were better correlated with those of desert soil colleted from desert regions in Inner Mongolia. Air mass back-trajectory analysis further confirmed that this dust storm event could be identified as streaks of dust plumes originating from Inner Mongolia.  相似文献   

6.
Data on deposition density of Ag, Al, As, B, Ba, Bi, Br, Ca, Cd, Co, Cr, Cs, Cu, Fe, K, Li, Mg, Mn, Mo, Na, Ni, P, Pb, Rb, S, Sb, Si, Sn, Sr, Th, Tl, U, V, Zn, Cl?, NO 3 ? , and SO4 4 2? in atmospheric precipitation were derived at 11 observation stations in the northern part of the European territory of Russia (ETR). Three sets (factors) of chemical indices that are mutually independent and determine the precipitation chemical content over that territory were revealed by using the hierarchical factor analysis of deposited density of chemical ingredients studied. These are two first-order factors: one is presented with the elements of a “marine” origin; the second is associated with biogenic elements. The second-order factor is formed by the ingredients characteristic of the combustion products of different fossil fuels. The structure and space-time distribution of factors are considered. The discriminant and cluster analyses allowed to classify the observation stations considered by the atmospheric precipitation chemistry and to show that Amderma, Vorkuta, Arkhangelsk, and Kargopol stations mostly differ from each other.  相似文献   

7.
Mass size distribution of the crustal elements (Al, Ca, Fe, Mg, Si, Ti), anthropogenic elements (Zn, Mn, Cr, Cu, K, P, Pb) and sea elements (Na, Cl) were obtained from measurements carried out with an inertial cascade impactor in Sfax. A fitting procedure by data inversion was applied to those data. This procedure yields accurate size distributions of aerosols in the diameter range 0.1–25 μm in two different sites. In a coastal industrial site, the mass distribution of the aerosol showed a bimodal structure; and in urban area, the lower particle mode cannot be observed. The elemental dry deposition flux was calculated as a function of particle size. The element flux size distribution increased rapidly with particle size. The modelling results indicate that the majority of the crustal and anthropogenic elements flux (>90%) was due to particles larger than 3 μm in diameter.  相似文献   

8.
Epidemiological studies initially considered the impact of total solid particles on human health, but according to the acquired knowledge about the worse effect of smaller particles, those studies turned to consider the impact of PM10. However, for the last decade PM2.5 began to be more important, once as they are smaller they can penetrate deeper in the lungs, being possible their trapping in alveoli and worse effects on human health. Therefore, more information on PM2.5 should be provided namely concerning the levels and elemental composition. Considering the relevance of traffic on the emission of particles of small sizes, this work included the detailed characterization of PM10 and PM2.5, sampled at two sites directly influenced by traffic, as well as at two reference sites, aiming a further evaluation of the influence of PM10 and PM2.5 on public health. The specific objectives were to study the influence of traffic emission on PM10 and PM2.5 characteristics, considering concentration, size distribution and elemental composition. PM10 and PM2.5 samples were collected using low-volume samplers; the element analyses were performed by particle induced X-ray emission (PIXE). At the sites influenced by traffic emissions PM10 and PM2.5 concentrations were 7–9 and 6–7 times higher than at the background sites. The presence of 17 elements (Mg, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn and Pb) was determined in both PM fractions; particle metal contents were 3–44 and 3–27 times higher for PM10 and PM2.5, respectively, than at the backgrounds sites. The elements originated mostly from anthropogenic activities (S, K, V, Mn, Ni, Zn and Pb) were predominantly present in PM2.5, while the elements mostly originated from crust (Mg, Al, Si and Ca) predominantly occurred in PM2.5–10. The results also showed that in coastal areas sea salt spray is an important source of particles, influencing PM concentration and distributions (PM10 increased by 46%, PM2.5/PM10 decreased by 26%), as well as PM compositions (Cl in PM10 was 11 times higher).  相似文献   

9.
To determine the effects of long-range transport of aerosols from an upwind area in East Asia to a downwind area in Japan, we chemically analyzed aerosols collected simultaneously on Tuoji Island (Shandong Province, China), Fukue Island (Nagasaki Prefecture, Japan), and Cape Hedo (Okinawa Prefecture, Japan). We focused on changes in the metallic composition of PM2.5 aerosols during long-range transport. The average mass concentrations of PM2.5 at the three sites decreased in the order Tuoji Island > Fukue Island ≈ Cape Hedo (48.3 ± 4.5, 13.9 ± 1.5, and 13.2 ± 0.9 μg/m3, respectively). The fraction of coarse particles in total suspended particles estimated by (1–PM2.5/TSP) was highest on Cape Hedo, indicating that the contribution of sea salts was increased by long-range transport of the aerosols over the ocean. Enrichment factor analysis revealed that at all three sites, Al, K, Ca, Mn, Fe, Co, Sr, and Ba originated from soil; whereas Cr, Ni, Cu, Zn, As, Mo, Ag, Cd, Sn, Sb, Tl, and P appeared to be of anthropogenic origin. Na was the most abundant element on Cape Hedo, indicating the addition of sea salts during aerosol transport. The V concentration was highest at Fukue Island, which was ascribed to V emission from ships. Sixty-one percent of the V on Fukue Island and 62% of the V on Cape Hedo were determined to have originated from ships, implicating of data obtained on dates during which backward trajectory analysis indicated that the same air mass passed over Tuoji Island, Fukue Island, and Cape Hedo in that order.  相似文献   

10.
The apportionment of atmospheric aerosols undertaken in Northern France during two sampling campaigns allowed to determine the influence of the atmospheric contribution of a heavy industrialized urban center on the particulate matter composition at a nearby rural site. The concentrations of major components and trace elements sampled by bulk filtration have been determined on June–July 2000 and January–February 2001, and the comparison of these two campaigns shows very well the importance of wind directions. The sources of 10 trace elements (Al, Ba, Cu, Fe, K, Mn, Pb, Sr, Ti and Zn) and 7 major components (Cl−, NO3−, SO42−, NH4+, Na, Mg and Ca) are better identified by studying their elemental contribution at each sampling site according to wind sectors. This kind of study shows that the concentrations recorded at the urban sampling site are always higher than those observed at the rural site as well during the summer campaign (about + 35%) as during the winter campaign (+ 90%), because of the predominance of the W–NW wind sector, corresponding to the influence of the urban and industrialized areas.  相似文献   

11.
The chemistry of rainwater was studied in three sites of a metropolitan city of Turkey to determine the spatial variation, sources affecting composition and the extent of their influence. The acidity of rainwater, Ca, Co, Cr, Zn, Ba, V and Ni showed significant spatial variations. The most of measured species were moderately to extremely enriched compared to the local soil, which is likely arisen from the anthropogenic activities. SO4 2?, K and Ca were found to be predominantly non-sea origin. Two receptor models, Positive Matrix Factorization (PMF) and Chemical Mass Balance (CMB), agreed well on the source contribution estimations of Al, K, Zn, V, Pb and Cr. The PMF and CMB resolved very similar source contribution profiles to the elemental concentrations of Ca, Zn, V, Pb, K and Na, which the majority of those resulted from mineral industries, bell casting+steel industries, fossil fuel burning, biomass burning+sea salt and sea salt, respectively. The PMF resolved the source contributions of long-transported emissions, particularly for Ba, Sr and Mn, which could not be estimated by the CMB.  相似文献   

12.
In the year 2000, the elemental composition of mosses collected from 528 French sites has been studied as part of the 2000 European Moss Survey. Five moss species were collected: Scleropodium purum (56%), Pleurozium schreberi (18%), Hypnum cupressiforme (18%), Thuidium tamariscinum (4.5%.) and Hylocomium splendens (3.5%). Mosses were kept whole for analysis, including green and brownish parts. Summary statistics on element concentrations (Al, Ba, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, Li, Mg, Mn, Na, Ni, P, Pb, Rb, Sr, V and Zn), and comparisons made with data from the other 27 participating European countries are shown here. The sources of these elements are identified using calculations of enrichment factors (EF) and principal component analysis (PCA). Finally, the spatial distribution in France of 10 elements is also shown, using maps underscoring areas showing highest concentration levels for each metal.  相似文献   

13.
Ambient suspended particles (TSP) were collected from January to June 2001 at seven sampling sites in western Macedonia, Greece, where four thermal power stations are located. TSP samples were chemically characterized for minerals (Fe, Al, Mg, Ca, K, Ti and Si), trace elements (P, Cd, Cr, Cu, Mn, Pb, V, Zn, Te, Co, Ni, Se, Sr, As, and Sb), water-soluble ions , carbonaceous compounds (OC/EC) and polycyclic aromatic hydrocarbons (PAHs). These classes of compounds were consequently compared with PM mass concentrations of TSP in order to perform mass closure. PM chemical compositions exhibited differences at the seven sites. Minerals were found to be more abundant at four sites, electrolytes dominated the composition at two of the sites while carbonaceous material was most abundant only at one site. The fraction unaccounted for ranged between 22 and 34%. Spatial variations of atmospheric concentrations showed significantly higher levels of minerals, some trace metals and TC at the site that was closest to the power plants. At the same site ions exhibited high correlations with minerals and the majority of trace elements.  相似文献   

14.
The compositions of TSP between AD and NAD storm periods were compared to study their long-term variations and chemical characteristics. TSP samples were collected at Gosan site in Jeju Island of Korea from February to May of 1992–2004. The major ionic and elemental species of TSP aerosols were analyzed. During AD periods, the concentrations of crust components (nss-Ca2+, Al, Fe, Ca, Mg, Ba, Sr, Ti) increased remarkably, and the concentrations of anthropogenic components (nss-SO42−, NO3−, S, Zn, Pb, Cr, Ni, Cd), with the exception of NH4+, increased weakly. The concentration ratios of all major components between AD and NAD periods showed ranges from 1.2 to 8.5, except for NH4+. The slope of the linear regression indicated that the contribution of CO32− may have comprised up to 17% of the total anions. Our results suggested that the AD storm greatly influenced TSP compositions. Linear regression analyses indicated that NH4+ was not correlated with NO3−, but highly correlated with nss-SO42− during both periods. The nss-SO42− was also correlated with NH4+, K+, nss-Mg2+, and nss-Ca2+ during both periods. Interestingly, NO3− was associated with nss-Ca2+ and nss-Mg2+ during AD periods. Of the metal elements, Fe, Ca, Mg, Ti, Mn, Ba, Sr, V, and Co were highly correlated with Al during both periods, signifying that these metals were mostly originated from soils.  相似文献   

15.
A study has been carried out on water soluble ions, trace elements, as well as PM2.5 and PM2.5–10 elemental and organic carbon samples collected daily from Central Taiwan over a one year period in 2005. A source apportionment study was performed, employing a Gaussian trajectory transfer coefficient model (GTx) to the results from 141 sets of PM2.5 and PM2.5–10 samples. Two different types of PM10 episodes, local pollution (LOP) and Asian dust storm (ADS) were observed in this study. The results revealed that relative high concentrations of secondary aerosols (NO3−, SO42− and NH4+) and the elements Cu, Zn, Cd, Pb and As were observed in PM2.5 during LOP periods. However, sea salt species (Na+ and Cl−) and crustal elements (e.g., Al, Fe, Mg, K, Ca and Ti) of PM2.5–10 showed a sharp increase during ADS periods. Anthropogenic source metals, Cu, Zn, Cd, Pb and As, as well as coarse nitrate also increased with ADS episodes. Moreover, reconstruction of aerosol compositions revealed that soil of PM2.5–10 elevated approximately 12–14% in ADS periods than LOP and Clear periods. A significantly high ratio of non-sea salt sulfate to elemental carbon (NSS-SO42−/EC) of PM2.5–10 during ADS periods was associated with higher concentrations of non-sea-salt sulfates from the industrial regions of China. Source apportionment analysis showed that 39% of PM10, 25% of PM2.5, 50% of PM2.5–10, 42% of sulfate and 30% of nitrate were attributable to the long range transport during ADS periods, respectively.  相似文献   

16.
To characterize atmospheric particulate matter equal or less than 2.5 μm in diameter (PM2.5) over the Tropical Atlantic Ocean, aerosol sampling was carried out in Puerto Rico during August and September, 2006. Aerosols were analyzed by ion chromatography for water-soluble inorganic and organic ions (including Na+, NH4 +, Mg2+, Ca2+, K+, Cl?, SO4 2?, NH4 +, F?, methanesulfonate (MSA), and oxalate), by inductive coupled plasma mass spectrometry (ICPMS) for trace elements (Al, Fe, Zn, Mn, Cu, Ni, V, Pb, Cr, Sb, Co, Sc, Cd), and by scanning electron microscopy for individual aerosol particle composition and morphology. The results show that the dominant cations in aerosols were Na+, (mean: 631 ng m?3), accounting for 63.8 % of the total cation and NH4 + (mean: 164 ng m?3), accounting for 13.8 % of the total cation measured in this study. The main inorganic anions were Cl? (576 ng m?3, 54.1 %) and SO4 2? (596 ng m?3, 38.0 %). The main organic anion was oxalate (18 ng m?3). Crustal enrichment factor calculations identified 62 % of the trace elements measured (Cu, Ni, V, Co, Al, Mn, Fe, Sc, and Cr) with crustal origin. Single particle analysis demonstrated that 40 % of the aerosol particles examined were Cl? rich particles as sodium chloride from seawater and 34 % of the total particles were Si-rich particles, mainly in the form of aluminosilicates from dust material. Based on the combination of air-mass trajectories, cluster analysis and principal component analysis, the major sources of these PM2.5 particles include marine, Saharan dust and biomass burning from West Africa; however, volcanic emissions from the Soufriere Hills in Montserrat had significant impact on aerosol composition in this region at the time of sample collection.  相似文献   

17.
The total suspended particulate (TSP) levels at Delhi (north India) were measured on 116 days between February and October 1980. The observations were stratified according to season and the values of cross-correlation of the TSP and its components were evaluated. High TSP (209 g m-3) levels were found during the summer period associated with hot and dry weather in the region and low TSP (109 g m-3) were found during the monsoon period. Most of the TSP mass was associated with natural soil elements, such as Fe, Al, Mn, Ca, and K. Only a fraction of the mass of the TSP was comprised of elements from anthropogenic sources, e.g., Pb, Ni, Cd, Sb, Cu, and Zn. The aerosols at Delhi were potentially basic in nature, unlike those in European countries which are acidic in nature and cause acid rainfall.  相似文献   

18.
An established three stage sequential leach scheme was applied to a series of selected high volume aerosol samples (n = 35) collected from the Turkish Eastern Mediterranean coastline (Erdemli). Samples were selected according to their air mass back trajectory history to reflect the contrasting mixtures of aerosol material present in the Eastern Mediterranean marine aerosol. Two populations were adopted, those samples which were classed as “anthropogenic” and those which were “Saharan” dominated aerosol populations. Applying the three stage leach it was possible to define the proportion for each of the considered metals (Al, Fe, Cu, Pb, Cd, Zn and Mn) present in the (a) “exchangeable” (b) “carbonate / oxide” and (c) “refractory” phases, representing novel solid state aerosol speciation data for this marine system. Clear trends were established, conforming with data from previous studies with mainly crustal derived metals (Al and Fe) being present in the refractory phases (Al > 88%; Fe > 84%) and those influenced by anthropogenic sources being dominating in the exchangeable phase, although for these metals the variability was comparatively high (12–64%; 19–85%; 40–100% for Zn, Pb and Cd, respectively). For the majority, greater exchangeable fractions were present the lower the crustal source contribution to the aerosol population, whereas the “refractory” fraction exhibited contrasting behaviour. This was illustrated by the novel application of the mixing diagram, presenting each of the three speciation stages against the corresponding percent anthropogenic contribution to each collected sample. Zn, Pb and Cd all illustrated progressive decrease in the percent exchangeable with increasing crustal contribution to the aerosol population. The percent exchangeable was discussed in terms of its use to represent the upper limit of the bioavailable fraction of metal associated with the aerosol, post deposition. The mixing diagram approach enabled the prediction of the residual fractions for Cd, Pb and Zn (41 ± 4%; 62 ± 4% and 82 ± 5%, respectively,) in Saharan end-member material.  相似文献   

19.
《Atmospheric Research》2005,73(1-2):87-100
Coarse (>2.2 μm) and fine (<2.2 μm) atmospheric particulate material samples were collected from an urban area (Al-Hashimya, Jordan), from August 2000 to August 2001 using a “GENT” stack filter unit (SFU). Collected samples were analyzed for 19 elements using inductively coupled plasma mass spectrometry (ICP-MS). The crustal elements exhibit atmospheric concentrations that are comparable to those in urban and industrial areas. The anthropogenic elements, on the other hand, are clearly less abundant in Al-Hashimya than in other industrial regions. Results indicated that, elements of crustal origin are associated with the coarse particles, while elements of anthropogenic origins are more associated with fine particles. Concentrations of crustal-derived elements were higher in summer and those of anthropogenic elements were higher in winter. Crustal enrichment factor calculations showed that concentrations of Pb, Zn, Cd, Sb and Ag are highly enriched and of As, Cu, Co, Ca and Ni are moderately enriched. Factor analysis calculations permitted the identification of four source groups for the fine fraction, namely oil combustion, crustal and urban dust, smelting industries and motor vehicles.  相似文献   

20.
大气气溶胶虚折射指数及其与元素的相关性   总被引：7，自引：1，他引：7       下载免费PDF全文
在西安、南京采集111个气溶胶样品，测定了虚折射率ni和分析了粒子中Si、Al、Ca、Fe、K、Mg、Mn、Na、Ti、S、P、Pb和Zn的含量。统计分析表明，ni与S和Pb的相关系数r最高，分别为0.36和0.30，统计检验也表明，这一相关性是显著的。其它11种元素与ni的相关性较差，且并不显著。西安气溶胶S含量明显高于南京，它与ni之间的相关系数高出南京近一倍。这些结果表明，除碳C之外，气溶胶中的S和Pb及其化合物对辐射的吸收不能忽视。  相似文献   

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