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1.
In‐situ aerosol measurements were performed in the northern hemispheric stratosphere up to altitudes of 21 km between 13 November 1996 and 14 January 1997, inside and outside of the polar vortex during the Airborne Polar Experiment (APE) field campaign. These are measurements of particle size distributions with a laser optical particle counter of the FSSP‐300 type operated during 9 flights on the Russian M‐55 high‐altitude research aircraft Geophysika. For specific flights, the FSSP‐300 measurements are compared with balloon‐borne data (launched from Kiruna, Sweden). It was found that the stratospheric aerosol content reached levels well below the background concentrations measured by the NASA operated ER‐2 in 1988/89 in the northern hemisphere. During the APE campaign, no PSC particle formation was observed at flight altitudes although the temperatures were below the NAT condensation point during one flight. The measured correlations between ozone and aerosol give an indication of the subsidence inside the 1996/97 polar vortex. Despite the lower aerosol content in the winter 1996/97 compared to the 1989 background, the heterogeneous reactivity of the aerosol (as calculated from the measured data with additional model input) is comparable. This is due to the dependency of the reactive uptake coefficients on the atmospheric water vapor content. Under the described assumptions the reaction rates on the background aerosol are significantly smaller than for competing gas phase chlorine activation, as can be expected for stratospheric background conditions especially inside the polar vortex.  相似文献   

2.
2008年北京奥运会期间大气气溶胶物理特征分析   总被引：5，自引：0，他引：5  
应用MODIS卫星的气溶胶产品资料和地面的光学粒子计数器的资料,对比分析了北京地区2006、2007、2008年7～9月的气溶胶光学厚度、细粒子光学厚度、Angstrom指数、气溶胶粒子数浓度谱及体积谱,发现2008年北京奥运会期间(7月20日～9月20日)的气溶胶光学厚度比2006、2007年同期明显降低,气溶胶细模态光学厚度占总光学厚度的比上升,Angstrom指数上升,气溶胶细粒子数浓度没有明显相对变化,而粗粒子数浓度则减少约50%.利用大气标高,将MODIS反演的气溶胶柱的质量浓度转化为地面气溶胶质量浓度.用粒子计数器得到的体积谱,在假定气溶胶粒子密度的情况下,计算出其质量浓度.将这两种方法得到的气溶胶质量浓度与国家环境保护部公布的空气质量指数换算得到的可吸入颗粒物(PM10)质量浓度进行比较.结果表明:北京奥运期间空气质量总体达到了国家二级空气质量标准;与2006、2007年同期相比,2008年气溶胶PM10质量浓度明显下降,而这主要是由气溶胶粗粒子的减少引起的.  相似文献   

3.
The change of the chemical composition of the near-ground level atmospheric aerosol was studied during two summer episodes by a Lagrangian type of experimental approach. Bulk and single-particle chemical analyses of ions and elements in the particulate phase were deployed. N(-III) and N(V) components were also measured in the gas-phase. The measurements were completed by particle size distributions.Secondary inorganic aerosols (SIA) and fine particles of ≈0.2–0.4 μm size were still elevated 50 km downwind of the city. The direct comparison of transport over the city in contrast to transport over the surrounding areas showed that SIA was formed from emission from the city within less than 3 h. Relative increases, i.e., enrichment during transport were observed for primary and secondary aerosol components. The degree of mixing on the individual particle level increased significantly during transport in the area. In particular, newly emitted carbonaceous particles became internally mixed within hours with pre-existing sulphate particles. Mostly due to secondary aerosol formation the average particle size (mass median diameter) of major constituents of the aerosol was significantly decreased while being transported over 13 h. Given recent insights which link fine particles number and mass concentrations with health risks, the results suggest that rural populations in areas which frequently are located within an urban plume might run an elevated health risk relative to populations in areas not affected by urban plumes.  相似文献   

4.
The first direct in situ measurements of the sulfuric acid contained in stratospheric aerosol particles were made using a novel balloon-based Ion Molecule Reaction Mass Spectrometer instrument (IMRMS) equipped with an aerosol vaporizer. The IMRMS method employed offers direct aerosol sulfuric acid measurements with high spatial resolution. The balloon flight took place on 23 October 1995 in middle latitudes (44°N) and reached a maximum altitude of 24 km. Measured molecular number densities of aerosol sulfuric acid decreased with increasing altitude from about 2.9 × 109 cm-3 at 15km altitude to about 2.4 × 108 cm-3 at 21 km. Corresponding mass mixing ratios are 2.5 and 0.6 ppbm, respectively. Calculated sulfuric acid mixing ratios from aerosol volumes inferred from aerosol size distribution measurements on the same balloon agree well with the IMRMS data using standard assumption aerosol composition.  相似文献   

5.
During May-June of 1990 an extensive flight series to survey aerosol present in the upper-troposphere was undertaken aboard the NASA DC-8 as part of the CLObal Backscatter Experiment (GLOBE). About 50,000 km were characterized between 8–12 km altitude and between 70°N and 58°S. Aerosol with diameters greater than 3nm were counted and sized with a combination of condensation nuclei counters and optical particle counters. Aerosol number and mass concentrations were separately identified with regard to both refractory and volatile components. Regions of the free-troposphere with the lowest mass concentrations were generally found to have the highest number concentrations and appeared to be effective regions for new particle production. These new particle concentrations appear inversely related to available aerosol surface area and their volatility suggests a sulfuric acid composition. The long lifetime of these new particles aloft can result in their growth to sizes effective as CN and CCN that can be mixed throughout the troposphere.  相似文献   

6.
Balloon-borne aerosol measurements were performed with an optical particle counter between 1994 and 2000 at Ny-Ålesund (79°N), Svarbard. Throughout the observation period, continuous decay was found in the concentrations of particles with 0.4–0.6 μm in radius in the Arctic stratosphere, suggesting that Pinatubo aerosols remained even at the end of the 1990s. The decay rate was clearly higher for larger particle sizes, and higher at higher altitude (e-folding time of 970–526 days), suggesting a gravitational sedimentation effect. For smaller particles with R<0.4 μm, slight increases in concentration with time were found, which agreed with the measurements at mid-latitude. The sulfate mass mixing ratio in the Arctic stratosphere before 1998 showed values higher than those at middle latitude, while values were almost the same in both regions after 1998. A possible explanation of the latitudinal difference is a time lag (of 0.5–1 year) in the arrival of Pinatubo aerosols in the Arctic.  相似文献   

7.
光电粒子计数器测量气溶胶折射指数虚部   总被引：3，自引：0，他引：3  
胡欢陵  许军 《大气科学》1991,15(5):18-24
本文分析了光电粒子计数器测量结果对气溶胶折射指数的敏感度,讨论了它测量的粒子谱分布与折射指数虚部n_i的相关关系。根据光电粒子计数器测量的粒子谱分布对n_i敏感的特点,利用光电粒子计数器和太阳辐射计同时测量的结果,可以确定气溶胶的n_i。实际测量的n_i值与积分片方法测量结果对比表明,这个方法是令人满意的。  相似文献   

8.
Aerosol optical parameters, polarized phase function and single-scattering albdeo, have been retrieved from ground-based sun photometer measurements in Beijing 2003. The measured aerosol optical thickness varies from 0.12 to 0.77 with an average value of 0.39. The measured Ångström coefficient ranges from 0.75 to 1.47 with an average value of 1.21. The retrieved single-scattering albedo at 870 nm is within the 0.76–0.94 range and the average value is 0.85, suggests there are considerable aerosol absorptions in Beijing. The maximum value of retrieved polarized phase function at 870 nm ranges from 0.068 to 0.225 with an average value of 0.16, and it illustrates good correlations with the Ångström coefficient, i.e. the relative size of aerosol particles. Analyses of measurements and theoretical calculations show the polarized phase function is sensitive to aerosol size distribution and complex refractive index, especially the imaginary part of the refractive index which denotes aerosol light absorbing effects. These results suggest that the polarized phase function is an effective and unique aerosol optical parameter and is able to improve the retrieval of aerosol physical properties.  相似文献   

9.
Characterization of aerosol optical properties, such as aerosol optical depth, Angstrom exponent, and volume size distribution at the semiarid site of Tombstone Arizona (31°23′N, 110°05′W, 1408 m) will be presented for one annual cycle. In this region, extensive observations of selected optical parameters such as aerosol optical depth (AOD) have been made in the past and reported on in the literature. Less is known about other optical characteristics that are important in climate modeling and remote sensing. New observational techniques and inversion methods allow for the expansion of the earlier information. Observations have been taken with a state of the art sun photometer for a 1-year period and their analysis will be presented here. Monthly mean AODs at 500 nm were found to be in the range of 0.03–0.12; the monthly mean Angstrom exponent ranged from 0.9 to 1.6, being higher in spring and summer and lower in late fall and winter. Volume size distributions exhibit clear dominance of smaller particles, with a gradual increase in size from winter to spring and into summer. Annual variation of the radii of the smaller and the larger particles ranged between 0.05–0.4 and 4–8 μm, respectively. Radiance measurements at 940 nm were used to estimate precipitable water. The retrieved values compared within limits of uncertainty with independently derived estimates from the National Center for Environmental Prediction (NCEP) regional weather forecast model. An interesting outcome from this study was the consistency found in aerosol optical depths as observed in this study and those derived about two decades ago.  相似文献   

10.
The atmospheric aerosol number concentration and size distribution were measured at six levels (50, 100, 150, 200, 250 and 300 m) on the Beijing 325 m meteorological tower by means of an optical particle counter. From the measured value of the concentration Nt and according to the expression Nz = Nce-ziRp, the value of aerosol scale height Hp was determined by using a least square method. An analysis shows that there are significant variations of aerosol concentration and size distribution in relation to time andaltitude. The average size distribution for each level can be described by (dN)/(dr)=arbe-er, where the parameters vary with the altitude.  相似文献   

11.
Precipitation scavenging of aerosol particles is an important removal process in the atmosphere that can change aerosol physical and optical properties. This paper analyzes the changes in aerosol physical and optical properties before and after four rain events using in situ observations of mass concentration, number concentration, particle size distribution, scattering and absorption coefficients of aerosols in June and July 2013 at the Xianghe comprehensive atmospheric observation station in China. The results show the effect of rain scavenging is related to the rain intensity and duration, the wind speed and direction. During the rain events, the temporal variation of aerosol number concentration was consistent with the variation in mass concentration, but their size-resolved scavenging ratios were different. After the rain events, the increase in aerosol mass concentration began with an increase in particles with diameter 0.8 μm [measured using an aerodynamic particle sizer(APS)], and fine particles with diameter 0.1 μm [measured using a scanning mobility particle sizer(SMPS)]. Rainfall was most efficient at removing particles with diameter ～0.6 μm and greater than 3.5 μm. The changes in peak values of the particle number distribution(measured using the SMPS) before and after the rain events reflect the strong scavenging effect on particles within the 100–120 nm size range. The variation patterns of aerosol scattering and absorption coefficients before and after the rain events were similar, but their scavenging ratios differed, which may have been related to the aerosol particle size distribution and chemical composition.  相似文献   

12.
北京地区气溶胶粒度谱分布初步研究   总被引：12，自引：0，他引：12  
本文对北京地区气溶胶数浓度及其诸分布特征进行了初步研究。重点探讨了气溶胶数浓度分布与相对湿度的关系。研究结果表明，气溶胶浓度和谱分布存在明显的日变化和逐日变化，并在很大程度上受空气相对湿度和理查森数影响。  相似文献   

13.
Surface measurements of aerosol physical properties were made at Anantapur(14.62°N,77.65 °E,331 m a.s.l),a semiarid rural site in India,during August 2008-July 2009.Measurements included the segregated sizes of aerosolsas as well as total mass concentration and size distributions of aerosols measured at low relative humidity(RH<75%) using a Quartz Crystal Microbalance(QCM) in the 25-0.05 μm aerodynamic diameter range.The hourly average total surface aerosol mass concentration in a day varied from 15 to 70 μg m-3,with a mean value of 34.02±9.05μgm-3 for the entire study period.A clear diurnal pattern appeared in coarse,accumulation and nucleation-mode particle concentrations,with two local maxima occurring in early morning and late evening hours.The concentration of coarse-mode particles was high during the summer season,with a maximum concentration of 11.81±0.98μgm-3 in the month of April,whereas accumulationmode concentration was observed to be high in the winter period contributed >68% to the total aerosol mass concentration.Accumulation aerosol mass fraction,A f(=Ma/Mt) was highest during winter(mean value of Af～0.80) and lowest(Af～0.64) during the monsoon season.The regression analysis shows that both R eff and R m are dependent on coarse-mode aerosols.The relationship between the simultaneous measurements of daily mean aerosol optical depth at 500 nm(AOD500) and PM 2.5 mass concentration([PM2.5]) shows that surface-level aerosol mass concentration increases with the increase in columnar aerosol optical depth over the observation period.  相似文献   

14.
An 8-wavelength sun-photometer has been operated at Hefei (31.31°N, 117.17°E) to monitoroptical properties of atmospheric aerosols. Altogether 133 solar spectral extinction data were ob-tained on clear days during the period from September 1993 through September 1994, In this pa-per, the feature of the sun-photometer is briefly described. A relative aureole method is intro-duced. which can be used to monitor temporal evolution of aerosol loading during the sun-pho-tometer calibration period. Temporal variabilities of spectral aerosol optical depths and Angstromturbidity parameters are presented. Relation of these variabilities with synoptic and local meteoro-logical conditions are analyzed and discussed, From measured spectral aerosol optical depths undersome representative atmospheric conditions, columnar aerosol size distributions have been retrievedby a linearly constrained inversion method. These typical columnar aerosol size distributions are al-so presented and discussed.  相似文献   

15.
During the spring of 2005, the total particle concentrations and the submicron aerosol size distributions were measured on board the research vessel over the south sea of Korea and the Korean sector of the Yellow Sea. Similar measurements were made over the East China Sea in autumn 2005. The aerosol properties varied dynamically according to the meteorological conditions, the proximity to the land masses and the air mass back trajectories. The average total particle concentration was the lowest over the East China Sea, 4335 ± 2736 cm− 3, but the instantaneous minimum, 837 cm− 3, for the entire ship measurement was recorded during the Yellow Sea cruise. There was also a long (more than 6 h) stretch of low total particle concentrations that fell as low as 1025 cm− 3 during the East China Sea cruise when the ship was the farthest from the shores and the air mass back trajectories resided long hours over the sea. These observations lead to the suggestion of ~ 1000 cm− 3 as the background total particle concentration over the marine boundary layer in the studied region of the Yellow Sea and the East China Sea, implying significant anthropogenic influence even for the background value. In the mean time, average aerosol size distributions were unimodal and the mode diameter ranged between 52 and 86 nm, excluding the fog periods, which suggests that the aerosols measured in this study experienced relatively less aging processes within the marine boundary layer.  相似文献   

16.
A comprehensive set of trace gas concentrations and meteorological parameters were measured simultaneously during a cruise of the research vessel Polarstern from Bremerhaven (54° N, 8° E) to Rio Grande (32° S, 52° W) during the period from 15 September to 9 October 1988. This paper describes the general features of the cruise and summarizes the measurements made, the techniques employed, and the placement of the instruments on board the ship. The synoptic data base is used to characterize the nature and possible origins of the air masses encountered during the cruise and to draw some general conclusions from the measurements.  相似文献   

17.
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   

18.
In this study, we present a relationship between total accumulation mode aerosol mass concentrations and cloud droplet number concentrations ( N d). The fundamental aim with the present method is to arrive at a physically‐based conversion algorithm in which each step in the conversion is based on real physical processes that occur and can be observed in the atmosphere, and in which all of the fields involved can be observed or modeled. In the last conversion (the critical part in the algorithm), we use measurements of the size distributions of cloud droplet residual particles for different pollution conditions. This conversion assumes that the size of the residual particles can be described with a lognormal distribution function and uses the Hatch–Choate relationship to convert between residual volume and number. The relatively sparse data set with which we have developed the present algorithm results in a course classification of the aerosol mass field. Consequently, uncertainties need to be recognized when using the algorithm in its present form in model calculations. The algorithm has been used on data from 15 days and the agreement between calculated and observed N d values is, with one exception, within a factor of 2 and for many of these cases also much better than a factor of 2. In addition to the results of the algorithm itself, we also present a least‐squares fit to the predicted N d values. To improve the algorithm in the longer‐term requires more data of scavenging fractions, particle chemical composition and density, and residual particle size distributions as a function of aerosol mass loading and cloud type.  相似文献   

19.
Aerosol particles were collected on filters for studies of their ability to nucleate ice during the second Arctic Gas and Aerosol Sampling Program (AGASP-II) in April, 1986. The ice nuclei (IN) samples were collected from an aircraft at altitudes ranging from the surface to the vicinity of the tropopause in Arctic locations over Alaska, northern Canada and Greenland. Samples of other components of the aerosol were collected and measurements were made of other properties of the aerosol coincident in time with the IN samples. The IN filters were exposed to water saturation in a dynamic developing chamber at –15° C and –25° C. Ice crystals grew on the IN and were counted on the filters at discrete time intervals during the exposure period to determine the rate of ice nucleation and the final concentration of (IN). Results show that Arctic haze aerosol, identified by pollutant signatures, had lower IN concentrations, a lower IN to total aerosol fraction and slower ice nucleation rates than aerosol which had a chemical signature more indicative of the remote unpolluted troposphere. These observations suggest that the Arctic haze aerosol does not efficiently form ice in the arctic troposphere. This may be a factor contributing to the long-range transport of Arctic haze.  相似文献   

20.
The performance of two different optical concentration-measuring techniques was investigated over a concentration range starting with about 102 cm−3 and extending over more than four decades. Both instruments are capable of real-time counting, however due to their particular design-single particle counter and ensemble particle-measuring system—they operate in overlapping, but different concentration ranges. The upper, coincidence-free counting limit for the single particle counter used in this study was established to be in the order of 104 cm−3. The ensemble technique was found to be functional and stable for concentrations of about 103 cm−3 and limited by the onset of multiple scattering at concentrations nearby 2×106 cm−3. Within the determined boundaries, both techniques proved to provide reliable aerosol concentration data.  相似文献   

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