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1.
The contribution of emissions from agricultural facilities is rapidly becoming a major concern for local and regional air quality. Characterization of particle properties such as physical size distribution and chemical composition can be valuable in understanding the processes contributing to emissions and ultimate fate of particulate matter from agricultural facilities. A measurement campaign was conducted at an Iowa, deep-pit, three-barn swine finishing facility to characterize near-source ambient particulate matter. Size-specific mass concentrations were determined using minivol samplers, with additional size distribution information obtain using optical particle counters. Particulate composition was determined via ion chromatographic analysis of the collected filters. A thermal-CO2 elemental/organic carbon analyzer measured particulate carbon. The chemical composition and size distribution of sub-micron particles were determined via real-time aerosol mass spectrometry. Primary particulate was not found to be a major emission from the examined facility, with filter-based impactor samples showing average near-source increases (~15–50 m) in ambient PM10 of 5.8 ± 2.9 μg m−3 above background levels. PM2.5 also showed contribution attributable to the facility (1.7 ± 1.1 μg m−3). Optical particle counter analysis of the numerical size distributions showed bimodal distributions for both the upwind and downwind conditions, with maximums around 2.5 μm and below the minimum quantified diameter of 0.3 μm. The distributions showed increased numbers of coarse particles (PM10) during periods when wind transport came from the barns, but the differences were not statistically significant at the 95% confidence level. The PM10 aerosols showed statistically increased concentrations of sulfate, nitrate, ammonium, calcium, organic carbon, and elemental carbon when the samplers were downwind from the pig barns. Organic carbon was the major constituent of the barn-impacted particulate matter in both sub-micron (54%) and coarse size (20%) ranges. The AMS PM1 chemical speciation showed similar species increases, with the exception of and Ca+2, the latter not quantified by the AMS.  相似文献   

2.
A time and height dependent eddy diffusion model is used to investigate possible scenarios for the size distribution of dust in the lower atmosphere of Mars. The dust is assumed to either have been advected from a distant source or to have originated locally. In the former case, the atmosphere is assumed to initially contain dust particles with sizes following a modified gamma distribution. Larger particles are deposited relatively rapidly while small particles are well mixed up to the maximum height of the afternoon boundary layer and are deposited more slowly. In other cases, a parameterization of the dust source at the surface is proposed. Model results show that smaller particles are rapidly mixed within the Martian boundary layer, while larger particles (r > 10 μm) are concentrated near the ground with a stronger diurnal cycle. In all simulations we assume that the initial concentration or surface source depend on a modified gamma function distribution. For small particles (cross- sectional area weighted mean radius, reff = 1.6 μm) distributions retain essentially the same form, though with variations in the mean and variance of the area-weighted radius, and the gamma function can be used to represent the particle size distribution reasonably well at most heights within the boundary layer. In the case of a surface source of larger particles (mean radius 50 μm) the modified gamma function does not fit the resulting particle size distribution. All results are normalised by a scaling factor that can be adjusted to correspond to an optical depth for assumed particle optical scattering properties.  相似文献   

3.
The fractions of local traffic (LT), urban background (UBG) and regional background (RBG) of the particle pollution at a traffic-influenced kerbside in Dresden, Germany, were determined by measurements of size-segregated mass concentration, chemical composition and particle size distributions in a network of five measurement stations partly existing and partly set up for this study. Besides the kerbside station, one urban background site and three rural sites were included in the study. Using data from these different sites, the LT, UBG, and RBG contributions were calculated, following the approach of Lenschow et al. (2001). At the kerbside site, 19% of the total number concentration (DpSt = 10–600 nm) could be attributed to the RBG, 15% to the UBG, and 66% to the LT immediately nearby. Particle mass concentrations up to Dpaer = 420 nm RBG amounts to 68%, UBG to 21%, and LT only to 11%. Highest mass concentrations were observed at all stations in autumn and winter during easterly inflow directions. The local traffic fraction of PM10 mass at the kerbside station was found to be 30% for westerly inflow, but only 7% for southeasterly inflow due to the dominating transport fraction from up to 80% of the particle mass at this inflow direction. Size-resolved investigation showed the main fractions in both the particle size ranges of Dpaer = 0.42 to 1.2 and 0.14 to 0.42 μm at all stations. The main components sulphate, ammonium and total carbon showed higher concentrations at south-eastern/eastern inflow in autumn at all stations, while nitrate at the kerbside and urban background site was higher during westerly inflow in winter. The chemical composition at the regional background site at westerly inflow (12% nitrate, 8% sulphate, 11% total carbon) was significantly different from that at easterly inflow (3% nitrate, 15% sulphate, 22% total carbon). The prevailing part of the ionic mass was always found in the fine particle range of Dpaer = 0.14 to 1.2 μm at all stations. For all inflow directions highest total carbon concentrations were observed at the kerbside station, especially in the ultra-fine size range of Dpaer = 0.05 to 0.14 μm with up to 30% of the whole carbon. PAH concentrations were always higher at south-eastern/eastern inflow especially during wintertime. Trace metal components and silicon were found mainly in the coarse mode fraction at the kerbside resulting from abrasion or resuspension.  相似文献   

4.
Daily measurements of atmospheric aerosol characteristics were carried out in Dolgoprudny (Moscow region) in June–August 2010. The particle concentrations at 11 size gradations within the range of 0.01–10 μm and the concentrations of cloud condensation nuclei active at water vapor supersaturation of 0.2–1% were determined. It is shown that the long anticyclonic conditions and the burning of forests and peat bogs resulted in the increase in total aerosol concentration in surface air by more than 1.5 times and in concentrations of particles with the diameter of 0.1–1 μm and > 1 μm by 5 and 10 times, respectively. The fire smoke mainly consisted of the particles with the size of 0.1–3 μm. The particles with the size of more than 5 μm were not observed. The recurrent visibility decrease up to hundreds of meters was caused by the increase in the concentration of particles with the diameter of more than 0.32μm in the air. During the smoke blanketing, the concentration of active condensation nuclei in aerosol increased almost by 20 times that created an opportunity for watering of aerosol particles and formation of the acid smog.  相似文献   

5.
Thin film methods and X ray energy dispersive technique were applied to analyze sulfate-containing particles in Beijing in order to examine their features and sources. Atmospheric aerosol particles were collected on electron mi-croscope meshes according to two size ranges: coarse particles (r>0.5μm) and fine particles (0.5μm≥r≥0.1μm) by using a two-stage impactor. It was found fiat more than seventy percent of the fine particles and about twenty percent of the coarse particles were sulfate-containing particles. These particles were formed mainly through heterogeneous nucleation. The element composition analyses revealed that the atmospheric aerosol particles in Beijing were domi-nated by crustal particles and construction dust.  相似文献   

6.
Research flights in November 1990 over the central parts of the United States, Wyoming and Colorado, were aimed to the investigation of the properties and microstructure of cirrus clouds (mainly cirrocumulus lenticularis). Among the other parameters measured on board the NCAR Saberliner were the concentration and size distribution of submicron particles and, in some cases, the particle deliquescence. For coarse insoluble particles found inside and outside of cloud elements, size distributions and morphology information were obtained by evaluating inertial impactor samples with an optical microscope and scanning electron microscope. In addition, the coarse particle composition was determined by x-ray energy spectrum analysis. The following conclusions from these measurements are:The large and coarse particle size distribution can be roughly simulated by a log-normal function with the modus around r=0.5 μm. Particle concentrations are very variable between several tenths and several particles per cm3. Particle volume distribution features a distinct maximum around 0.75 μm without a broad plateau which was observed in the case of sampling at lower altitude. Aerosol composition heterogeneity at cirrus cloud level is well documented by the evaluation of the fine particle sampling taken with the UMR sampling system. This heterogeneity can be partly explained by the interaction between aerosol and cloud elements, which is documented by the measured particle size distribution curves inside and outside of cloud elements. Assuming that particle deliquescence is caused by H2SO4 and/or by (NH4)2SO4, particle soluble mass fractions were found to be around 30% in the first case and about 40% in the second. The most frequently occurring elements in large and coarse particles at cirrus cloud level were Si, Cl, Ba, S, Ca and C.  相似文献   

7.
This work attempts to characterize metallic elements associated with atmospheric particulate matter on a dry deposition plate, a TE-PUF high-volume air sampler and a universal air sampler. Dry deposition fluxes of particulates and concentrations of total suspended particulate, fine (PM2.5) and coarse (PM2.5–10) particulate matters were collected at Taichung harbor sampling sites from August 2004 to January 2005. Chemical analyses of metallic elements were made using a flame atomic absorption spectrophotometer coupled with hollow cathode lamps. Concentrations of metal elements in the forms of coarse particles and fine particles as well as the coarse/fine particulate ratios were presented. Statistical methods such as correlation analysis, principal component analysis and enrichment factor analysis were performed to compare the chemical components and identify possible emission sources at the sampling sites. Metallic elements of Cu, Zn, Pb, Cr, Ni and Mg had higher EFcrust ratios in winter and spring than in summer and autumn. Diurnal and nocturnal variations of metallic element concentrations in fine and coarse particles were also discussed.  相似文献   

8.
Total suspended particulates(TSP)samples were collected using low pressure impactors(Andersen Series 20-800,USA)on typical clear,hazy and foggy days in Beijing in order to investigate the characteristics of size distributions and elemental compositions of particulate matter(PM)in different weather conditions. The concentrations of sixteen elements,including Na,Mg,Al,K,Ca,Mn,Fe,Ni,Cu,Zn,As,Se,Cd,Ba,Tl and Pb were detected using inductively coupled plasma mass spectrometry(ICP-MS).The results showed that Ca,Al,Fe,Mg and Ba on foggy days were 2.0-2.6 times higher than on clear days,and 2.3-2.9 times higher than on hazy days.Concentrations of Cu,Zn,As,Se and Pb on foggy days were 163.5,1186.7,65.9,32.0 and 708.2 ng m-3,respectively,in fine particles,and 68.1,289.5,19.8,1.6 and 103.8 ng m-3,respectively,in coarse particles.This was 1.0-8.4 times higher and 1.4-7.4 times higher than on clear and hazy days,respectively.It is then shown that Mg,Al,Fe,Ca and Ba were mainly associated with coarse particles,peaking at 4.7-5.8μm;that Cd,Se,Zn,As,Tl and Pb were most dominant in fine particles,peaking at 0.43-1.1μm;and that Na,K,Ni,Cu and Mn had a multi-mode distribution,with peaks at 0.43-1.1μm and 4.7-5.8μm.The enrichment factors indicated that coal combustion along with vehicle and industry emissions may be the main sources of pollution elements.  相似文献   

9.
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   

10.
Samples of airborne PM2.5 particles in Guangzhou urban area were collected during the autumn of 2006 and the spring of 2007. The morphologies and elemental compositions of individual particles were determined by Scanning Electron Microscopy coupled with Energy Dispersive X-ray Spectrometer (SEM-EDX). The obtained images were further analyzed for size distribution by an image analysis system. Based on the morphology, particles in PM2.5 were classified into four groups: soot aggregates, minerals, fly ash and others. The amount of soot aggregates and minerals were higher than that of fly ashes. The distributions of particles by number and size in two seasons were bimodal with 90% less than 1.0 μm in diameter. The primary peak from the autumn samples was in the size range of 0.4 ~ 0.5 μm, and 0.3 ~ 0.4 μm for the spring samples. More soot aggregates (36.1%) and minerals (61.5%) were found than fly ash (2.4%) in autumn, but soot aggregates (89.9%) was the dominant particle type in spring. The size distribution of particles according to the volume was generally opposite to that according to the number. Particles less than 1.0 μm were as high as 89.5% in number but contributed only 18.9% in volume, indicating that fine particles contributed relatively little in volume although existing in large numbers.  相似文献   

11.
The seasonal variations of the concentration of particles of different sizes in the atmospheric surface layer are studied on the basis of the data of daily measurements of atmospheric aerosol characteristics in the town of Dolgoprudny (20 km from the center of Moscow) carried out in 2006–2009. It is revealed that the steady variations of monthly mean aerosol concentration are observed within the particle diameter interval of 0.02–1 μm. The annual course of concentration of these particles has two maxima, in February-March and in September–October, and one minimum in June. The concentrations of particles with the size of 0.01–0.02 μm defined by the general atmospheric background and the concentrations of particles of >1 μm associated with the local sources do not have clearly pronounced seasonal variations. It is shown that the regularities of the annual concentration variations of particles with the size of 0.02–1 μm are mainly explained by the sign and value of the lapse rate in the layer up to 925 hPa that indicates the prevalence of the vertical mixing in the processes of aerosol scattering in the surface layer as compared with the horizontal transfer.  相似文献   

12.
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   

13.
A chemical substance being in a high-disperse state (fine aerosol particles and very thin films) in the environment reveals specific chemical and physicochemical features which differ from the processes in a relatively coarse disperse object and, even more, in ordinary liquid and solid “test-tube” assays. The kinetics and the mechanism of the direct and sensitized photochemical destruction of pesticide compound fipronil C12H4Cl2F6N4OS have been experimented as applied to the aerosol particles ≈0.12–1.3 μm in diameter and thin films ≈0.02–0.6 μm thick on the glass plates. A non-photochemical (“dark”) reaction of fipronil molecules with the OH radicals which spontaneously proceeds in the ambient air was also observed. Quantitative estimations based on experimental results show that the fipronil pollutant, observed in the atmosphere in the form of levitated aerosols, can convert chemically in the above reaction with the OH radicals for a very short time (from several minutes for a particle 2 μm in diameter to 12–24 h for a particle of 20–30 μm). The fipronil residues presented on foliage either in the form of 1–20 μm films or as a group of deposited 2–30 μm aerosols react under sunlight by two photochemical pathways (photooxidation and photodecay). The lifetime of these residues in the ambient conditions is expected to be 11–25 days. Besides, adding a small amount of the Shirvanol 2 sensitizer to the fipronil formulation, one can increase the overall decomposition rate to 8–12 days.  相似文献   

14.
Secondary aerosol formation was studied at Allahabad in the Indo-Gangetic region during a field campaign called Land Campaign-II in December 2004 (northern winter). Regional source locations of the ionic species in PM10 were identified by using Potential Source Contribution Function (PSCF analysis). On an average, the concentration of water soluble inorganic ions (sum of anions and cations) was 63.2 μgm−3. Amongst the water soluble ions, average NO3− concentration was the highest (25.0 μgm−3) followed by SO42− (15.8 μgm−3) and NH4+ (13.8 μgm−3) concentrations. These species, contributed 87% of the total mass of water soluble species, indicating that most of the water soluble PM10 was composed of NH4NO3 and (NH4)2SO4/NH4HSO4 or (NH4)3H(SO4)2 particles. Further, the concentrations of SO42−, NO3−, and NH4+ aerosols increased at high relative humidity levels up to the deliquescence point (∼63% RH) for salts of these species suggesting that high humidity levels favor the conversion and partitioning of gaseous SO2, NOx, and NH3 to their aerosol phase. Additionally, lowering of ambient temperature as the winter progressed also resulted in an increase of NO3− and NH4+ concentrations, probably due to the semi volatile nature of ammonium nitrate. PSCF analysis identified regions along the Indo-Gangetic Plain (IGP) including Northern and Central Uttar Pradesh, Punjab, Haryana, Northern Pakistan, and parts of Rajasthan as source regions of airborne nitrate. Similar source regions, along with Northeastern Madhya Pradesh were identified for sulfate.  相似文献   

15.
The concentrations of PM10, PM2.5 and their water-soluble ionic species were determined for the samples collected during January to December, 2007 at New Delhi (28.63° N, 77.18° E), India. The annual mean PM10 and PM2.5 concentrations (± standard deviation) were about 219 (± 84) and 97 (±56) μgm−3 respectively, about twice the prescribed Indian National Ambient Air Quality Standards values. The monthly average ratio of PM2.5/PM10 varied between 0.18 (June) and 0.86 (February) with an annual mean of ∼0.48 (±0.2), suggesting the dominance of coarser in summer and fine size particles in winter. The difference between the concentrations of PM10 and PM2.5, is deemed as the contribution of the coarse fraction (PM10−2.5). The analyzed coarse fractions mainly composed of secondary inorganic aerosols species (16.0 μgm−3, 13.07%), mineral matter (12.32 μgm−3, 10.06%) and salt particles (4.92 μgm−3, 4.02%). PM2.5 are mainly made up of undetermined fractions (39.46 μgm−3, 40.9%), secondary inorganic aerosols (26.15 μgm−3, 27.1%), salt aerosols (22.48 μgm−3, 23.3%) and mineral matter (8.41 μgm−3, 8.7%). The black carbon aerosols concentrations measured at a nearby (∼300 m) location to aerosol sampling site, registered an annual mean of ∼14 (±12) μgm−3, which is significantly large compared to those observed at other locations in India. The source identifications are made for the ionic species in PM10 and PM2.5. The results are discussed by way of correlations and factor analyses. The significant correlations of Cl−, SO42−, K+, Na+, Ca2+, NO3− and Mg2+ with PM2.5 on one hand and Mg2+ with PM10 on the other suggest the dominance of anthropogenic and soil origin aerosols in Delhi.  相似文献   

16.
Long-term measurements of ambient particulate matter less than 2.5 μm in diameter (PM2.5) and its chemical compositions were performed at a rural site in Korea from December 2005 to August 2009. The average PM2.5 concentration was 31 μg m−3 for the whole sampling period, and showed a slightly downward annual trend. The major components of PM2.5 were organic carbon, SO42−, NO3−, and NH4+, which accounted for 55 % of total PM2.5 mass on average. For the top 10 % of PM2.5 samples, anionic constituents and trace elements clearly increased while carbonaceous constituents and NH4+ remained relatively constant. Both Asian dust and fog events clearly increased PM2.5 concentrations, but affected its chemical composition differently. While trace elements significantly increased during Asian dust events, NO3−, NH4+ and Cl were dramatically enhanced during fog events due to the formation of saturated or supersaturated salt solution. The back-trajectory based model, PSCF (Potential Source Contribution Function) identified the major industrial areas in Eastern China as the possible source areas for the high PM2.5 concentrations at the sampling site. Using factor analysis, soil, combustion processes, non-metal manufacture, and secondary PM2.5 sources accounted for 77 % of the total explained variance.  相似文献   

17.
PM10 samples were collected over three years at Monzenmachi, the Japan Sea coast, the Noto Peninsula, Ishikawa, Japan from January 17, 2001 to December 18, 2003, using a high volume air sampler with quartz filters. The concentrations of the water-soluble inorganic ions in PM10 were determined with using ion chromatography. By analyzing the characteristics of these, the evidences were found that the Asian outflow had an obviously influence on the air quality at our study site. The results were as follows: the secondary pollutants SO42−, NO3− and NH4+ were the primary water-soluble inorganic ions at our study site. The monthly mean concentrations of SO42−, NH4+, NO3− and Ca2+ have prominent peak in spring due to the strong influence of the Asian continent outflow—these according to backward air trajectory analysis, the maximum of which were 6.09 for nss-SO42− in May, 2.87 for NO3− and 0.68 μg m−3 for nss-Ca2+ in April, respectively. Comparable to similar data reported from various points around East Asia, it had the characteristics of a polluted coastal area at our study site. The concentration of nss-Ca2+ in PM10 drastically increased when the Asian dust invaded, the mean value during the Asian dust days(AD) was 0.86 μg m−3, about 4 times higher than those of normal days (NAD). Meanwhile, the mean concentrations of nss-SO42−, NO3− and NH4+ in AD periods were higher than those in NAD periods which were 5.87, 1.76 and 1.82 μg m−3, respectively, it is due to the interaction between dust and secondary particles during the long-range transport of dust storms. Finally, according to the source apportionment with positive matrix factorization (PMF) method in this study, the major source profiles of PM10 at our study site were categorized as (1) marine salt, (2) secondary sulfate, (3) secondary nitrate and (4) crustal source.  相似文献   

18.
Ambient concentrations of polycyclic aromatic hydrocarbons (PAHs) were measured in Helsinki (Finland). Particle mass size distributions were obtained with a cascade impactor (12 stages) with glass fibre filters as substrates. Simultaneously with the impactor measurements, particulate and gaseous PAHs were collected on a quartz filter and XAD-2 adsorbent, respectively, for evaluation of gas-partition coefficients. Samples were analysed for PAHs by on-line coupled supercritical fluid extraction — liquid chromatography — gas chromatography — mass spectrometry. The impactor results showed that most of the PAHs in Helsinki urban area were concentrated in fine particles (<2.5 μm diameter) with unimode peak at about 1 μm. The results were comparable with the number distribution measured with a differential mobility particle sizer. Total amounts of PAHs (gas + particle) varied from 15 (acenaphthylene) to 1990 (fluorene) pg/m3. The PAHs lighter than 202 amu (pyrene and fluoranthene) were exclusively in gas phase, whereas those heavier than 202 amu were mostly associated with particles. A plot of the partition coefficients (logKp) versus the temperature dependent sub-cooled vapour pressures (logp L 0 ) showed a gradient of −0.66, which deviated from equilibrium state (gradient = −1).  相似文献   

19.
Ice samples from the 905 m deep Dome C core (East Antarctica) were studied in terms of insoluble microparticle contents. Various techniques were used: right angle light scattering, nephelometer (multiangle light scattering), Coulter counter and microscope analyses, in order to make a thorough study of the physical and optical properties of microparticles and their variations over the last 30000 years. Because of the possible effect of atmospheric turbidity on the earth-atmosphere radiation balance, optical parameters of climatic importance were estimated for insoluble microparticles. The detailed profile of total microparticle mass concentrations shows a drastic (factor of 17 ± 13) difference between high Last Glacial Maximum (LGM) and low Holocene concentrations. The optical scattering properties of 18000 BP continental dust do not indicate a significant difference with respect to Holocene dust in terms of particle size distribution and complex refractive index. The number to log radius size distribution of microparticles for the entire 30 000 yr period can be fitted by a log-normal distribution with two parameters (modal radius 0.25 ± 0.08 μm; geometric standard deviation 2.2. ± 0.2). However, for the smallest particles a better adjustment between experimental and theoretical scattering diagrams is obtained by adding to the observed size distribution another log-normal distribution (modal radius = 0.025 μm, σ g = 2). The complex refractive index is 1.53 to 1.56 for the real part and 0.005 ± 0.005 for the imaginary part at the wavelength used (λ= 546 nm). During the LGM stage, over the whole of Antarctica, the change in the total optical depth due to the drastic change in the insoluble aerosol loading is small because insoluble impurities are not the dominant aerosol component. It may have produced a slight warming of the snow surface (≈ 2 K). In the dust source regions, the optical depth would have been a maximum of 2 to 4 times the present value. The possible warming of the atmosphere in these regions is estimated at 3 K per day and should therefore be taken into account in paleoclimate reconstruction models.  相似文献   

20.
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   

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