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1.
We propose an analytical expression for the relation between aerosol accumulation number and sub‐micron volume over the marine boundary layer (MBL), based on a simple balance equation. By providing appropriate source and sink terms which account for entrainment, coagulation, in‐cloud scavenging and condensational growth, the model is able to reproduce the observed ratio between MBL particles larger than 80 nm diameter (as a proxy for accumulation mode number) and submicron aerosol volume, from freshly polluted to background conditions. Entrainment and coagulation are essential in predicting the observed ratio. Budget and lifetime calculations show that, due to relatively low source rates of oceanic non‐sea‐salt‐sulfate and sea‐salt, the anthropogenic signature in aerosol volume remains significant even after 8 days of MBL transport.  相似文献   

2.
利用AERONET观测资料从气候学的角度比较分析了2001-2011年东亚地区沙尘天气发生时沙尘源区和下游区大气气溶胶光学特性。结果表明：沙尘期间沙尘源区气溶胶光学厚度明显大于下游区,而Angstr?m波长指数却小于下游区,当沙尘暴出现时会降至零甚至负值。气溶胶粒子尺度体积谱分布除敦煌为单峰外,其余各站均呈双峰分布,香河和北京的细粒子浓度明显大于西北地区,这可能是由细的沙尘粒子和污染气溶胶共同造成。在440-1020 nm范围内,中国地区气溶胶单次散射反照率平均值为0.93,韩国和日本站分别为0.93和0.94。沙尘源区与下游区相比,复折射指数实部偏大,虚部偏小。总体来说,沙尘天气下东亚地区在4个波段内平均不对称因子为0.70。  相似文献   

3.
The aerosol number spectrum and gas pollutants were measured and the new particle formation （NPF） events were discussed in Nanjing. The results showed that the size distributions of aerosol number concen- trations exhibited distinct seasonal variations, implying the relations of particle sizes and their sources and sinks. The number concentrations of particles in the nuclei mode （10-30 nm）, Aitken mode （30-100 nm）, accumulation mode （100 -1000 nm） and coarse mode （〉1μm） varied in the order of summer 〉 spring 〉 autumn, summer 〉 autumn 〉 spring, autumn 〉 summer 〉 spring, and spring 〉 autumn 〉summer, re- spectively. The diurnal variation of total aerosol number concentrations showed three peaks in all observed periods, which corresponded to two rush hours and the photochemistry period at noon. In general, the NPF in summer occurred under the conditions of east winds and dominant air masses originating from marine areas with high relative humidity （50%-70%） and strong solar radiations （400 -700 W m-2）. In spring, the NPF were generally accompanied by low relative humidity （14%-30%） and strong solar radiations （400-600 W m-2）. The new particle growth rates （GR） were higher in the summertime in the range of 10- 16 nm h-1. In spring, the GR were 6.8-8.3 nm h-1. Under polluted air conditions, NPF events were seldom captured in autumn in Nanjing. During NPF periods, positive correlations between 10- 30 nm particles and 03 were detected, particularly in spring, indicating that NPF can be attributed to photochemical reactions.  相似文献   

4.
Long-term measurements of fine particle number-size distributions were carried out over 9.5 yr (May 1997–December 2006), in the urban background atmosphere of Helsinki. The total number of days was 3528 with about 91.9% valid data. A new particle formation event (NPF) is defined if a distinct nucleation mode of aerosol particles is observed below 25 nm for several hours, and it shows a growth pattern. We observed 185 NPF events, 111 d were clear non-events and most of the days (around 83.5%) were undefined. The observed events were regional because they were observed at Hyytiälä (250 km north of Helsinki). The events occurred most frequently during spring and autumn. The observed formation rate was maximum during the spring and summer (monthly median 2.87 cm−3 s−1) and the modal growth rate was maximum during late summer and Autumn (monthly median 6.55 nm h−1). The events were observed around noon, and the growth pattern often continued on the following day. The observation of weak NPF events was hindered due to pre-existing particles from both local sources. It is clear that regional NPF events have a clear influence on the dynamic behaviour of aerosol particles in the urban atmosphere.  相似文献   

5.
Patterns of propagation of aerosol particles generated in the hygroscopic seeding of convective clouds from antihail rockets is studied. Effects of the salt particle dispersity on condensational growth rate of separate cloud droplets on these particles are studied; analytical formulas are obtained as describing change of radius of the NaCl crystal and of the cloud droplet which grows on the crystal till the moment of full dissolving of the crystal in the droplet. Numerical computations are used for comparative analysis of the salt effect on intensification of condensational growth of the droplets in the cloud.  相似文献   

6.
通过实验收集大气颗粒物，对南京地区大气气溶胶谱分布进行了描述，对气溶胶分布与相对湿度的相关性进行了探讨。建立了南京地区7—11月气溶胶化学组分的月平均模型，得出气溶胶等效复折射率的预测方法。结果表明：南京地区的大气气溶胶颗粒物，峰值粒径在80~100 nm范围，属于典型的城市型气溶胶。数浓度与相对湿度的相关性与季节和粒径大小有关，在6—9月，相对湿度与细粒子数浓度呈负相关，与粗粒子呈正相关，在10—11月相反，且易受极端天气影响。建立的干气溶胶等效复折射率月平均模型，结合湿度修正模型得到某一日的复折射率，与AERONET站点数据进行了对比，结果较为一致，误差范围在0~0.03。  相似文献   

7.
Ground-based aerosol instrumentation covering particle size diameters from 25 nm to 32 µm was deployed to determine aerosol concentration and cloud condensation nuclei (CCN)-activation properties at water vapor supersaturations in the range of S = 0.20–1.50 % in the remote Brazilian northeast semi-arid region (NEB) in coastal (maritime) and continental (inland) regimes. The instruments measured aerosol number concentration and activation spectra for CCN and revealed that aerosol properties are sensitive with respect to the sources as a function of the local wind circulation system. The observations show that coastal aerosol total number concentrations are above 3,000 cm?3 on average, exhibiting concentration peaks depending on the time of the day in a consistent daily pattern. The variation on aerosol concentration has also influences on the fraction of particles active as CCN. At 1.0 % water vapor supersaturation, the fraction can reach as high as 80 %. Inland aerosol total concentrations were about 1,800–1,900 cm?3 and did not show much diurnal variation. The fraction of particles active as CCN observed inland depend on the history of the air masses, and was much higher when air masses were originated over the sea. It was found that (NH4)2SO4 and NaCl are the major soluble inorganic fraction of the aerosols at the coast. The major fraction of NaCl was present in the coarse mode, while ammonium sulfate dominates the inorganic fraction at the submicron range, with about 10 % of the total aerosol mass at 0.32 µm. Inorganic compounds are almost absent in particles with sizes around 0.1 μm. The study suggests that the air masses with high concentration of CCN originate at the sea. The feasible explanation lies in the fact that the NEB’s beaches have a particular morphology that produces a wide surf zone and creates a large load of aerosols when combined with strong and permanent winds of the region.  相似文献   

8.
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   

9.
城市地区大气气溶胶颗粒的物理化学特性复杂,理清单颗粒精细的化学成分和混合状态对于大气污染溯源和精细治理具有重要意义。本研究利用被动式气溶胶采样器分别在山东省日照市城区和钢铁园区两个区域进行了定点采样,并利用智能扫描电镜环境颗粒物分析系统（IntelliSEM EPAS）对采集的大气单颗粒物样品进行分析。结果表明,日照市大气颗粒物主要由不规则碳质颗粒（C-rich）、含硫颗粒（Ca-S、Na-S-Ca）与矿物颗粒组成。其中,城区样品中C-rich颗粒数量贡献为53.5%,是钢铁园区样品的2.5倍,大于1 μm的颗粒物数量为9.0%,是钢铁园区样品的1.7倍,城区居民活动和工业过程是城市中大气颗粒物特别是二次细颗粒的主要来源。钢铁园区样品中含硫颗粒物数量贡献为72.9%,含硫颗粒物质量贡献为30.9%,富铁颗粒物质量贡献为5.3%,分别是城区样品的1.8倍、3.6倍和2.9倍,表明钢铁园区大气颗粒物的主要来源包括钢铁企业排放的一次污染物及其转化生成的二次细颗粒物。  相似文献   

10.
Particle number size distribution(PNSD) between 10 nm and 20 μm were measured in the Pearl River Delta(PRD) region in winter 2011.The average particle number concentration of the nucleation mode(10-20 nm),Aitken mode(20-100 nm),accumulation mode(100 nm-1μm) and coarse mode(1-20 μm) particles were 1 552,7 470,4 012,and 19 cm-3,respectively.The volume concentration of accumulation mode particles with peak at 300 nm accounted for over 70% of the total volume concentration.Diurnal variations and dependencies on meteorological parameters of PNSD were investigated.The diurnal variation of nucleation mode particles was mainly influenced by new particle formation events,while the diurnal variation of Aitken mode particles correlated to the traffic emission and the growth process of nucleation mode particles.When the PRD region was controlled by a cold high pressure,conditions of low relative humidity,high wind speed and strong radiation are favorable for the occurrence of new particle formation(NPF) events.The frequency of occurrence of NPF events was 21.3% during the whole measurement period.Parameters describing NPF events,including growth rate(GR) and source rate of condensable vapor(Q),were slightly larger than those in previous literature.This suggests that intense photochemical and biological activities may be the source of condensable vapor for particle growth,even during winter in the PRD.  相似文献   

11.
2006年北京春季气溶胶吸收系数的分离研究   总被引：3，自引：0，他引：3  
对2006年春季北京城区大气气溶胶中沙尘和黑碳气溶胶吸收系数的波长指数及其对总吸收系数的贡献进行了估算。结果表明：2006年春季北京城市地区测点,黑碳气溶胶吸收系数随波长的变化呈指数递减,假设某些天的气溶胶吸收无沙尘的贡献,估算的波长幂指数a＝-0.92。另外,计算了北京3次浮尘天气下沙尘气溶胶对吸收系数（520 nm波段）的贡献,计算表明,在浮尘天气影响期间,沙尘气溶胶对吸收系数的贡献平均为32.8%,黑碳气溶胶仍是浮尘影响期间城市气溶胶吸收消光的主要物质。  相似文献   

12.
Aerosol size spectra (d=10 nm–10 μm) were measured with an electrical aerosol spectrometer (EAS) at Mace Head on the west coast of Ireland. Several small aerosol particle (diameter 10–32 nm) concentration bursts were observed during the measurement period. Relationships between the events, air mass trajectories, tide height, and meteorological parameters are examined. Series of bursts were observed when a spectral transformation due to subsequent particle growth from 10 to 56–100 nm can be identified in an Eulerian experiment. Particle growth rates of between 1 and 3 nm/h were determined. These bursts appear in cold and comparatively clean arctic or polar air masses with temperature and relative humidity fluctuations, and do not correlate with low tide in some cases. These episodes, similar to those frequently found in the continental boundary layer, are thought to occur over a wide area and, for clear detection, require stable airflow for a few days. Elevated small-particle concentration events are more common during low tide or shortly after, and are typically associated with low wind speeds. Here, the increased shore exposure during low tide is thought to influence the nucleation and the subsequent growth of these aerosol particles. The occurrences of the bursts are found to depend on local wind direction. The highest d=10–32 nm particle concentrations appeared for wind sectors furthest from the tidal regions when the wind direction was 150–160°(south-easterly). Most of the events occurred during daytime when solar irradiation is most intense.  相似文献   

13.
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   

14.
 A statistic regression approach was used to estimate the wavelength exponents of black carbon (BC) and dust particles, and further to separate the contributions of the two types of aerosols to the total light absorption coefficient measured in the Beijing urban area in the spring of 2006. The results show that the wavelength exponent (a) of black carbon aerosol at urban site was approximately -0.92, which is in agreement with the value of -0.8±0.2 reported in related studies. The decoupling analysis of the measured light absorption coefficients during the three floating dust periods ( March 25, March 27, and April 9) demonstrates that, on average, the light absorption caused by dust particles took up about 32.8% of the total light absorption at 520 nm wavelength, and by black aerosol more than 60%. This indicates that the black carbon was still the major contributor to the total aerosol light absorption in Beijing urban area even during the floating dust periods.  相似文献   

15.
Aerosol optical properties and direct radiative effects on surface irradiance were examined using seven years(2006–2012)of Cimel sunphotometer data collected at Panyu—the main atmospheric composition monitoring station in the Pearl River Delta(PRD) region of China. During the dry season(October to February), mean values of the aerosol optical depth(AOD)at 550 nm, the ?ngstr?m exponent, and the single scattering albedo at 440 nm(SSA) were 0.54, 1.33 and 0.87, respectively.About 90% of aerosols were dominated by fine-mode strongly absorbing particles. The size distribution was bimodal, with fine-mode particles dominating. The fine mode showed a peak at a radius of 0.12 μm in February and October(~0.10μm~3μm~(-2)). The mean diurnal shortwave direct radiative forcing at the surface, inside the atmosphere(FATM), and at the top of the atmosphere, was-33.4 ± 7.0, 26.1 ± 5.6 and-7.3 ± 2.7 W m~(-2), respectively. The corresponding mean values of aerosol direct shortwave radiative forcing per AOD were-60.0 ± 7.8, 47.3 ± 8.3 and-12.8 ± 3.1 W m~(-2), respectively. Moreover,during the study period, FATMshowed a significant decreasing trend(p 0.01) and SSA increased from 0.87 in 2006 to 0.91 in 2012, suggesting a decreasing trend of absorbing particles being released into the atmosphere. Optical properties and radiative impacts of the absorbing particles can be used to improve the accuracy of inversion algorithms for satellite-based aerosol retrievals in the PRD region and to better constrain the climate effect of aerosols in climate models.  相似文献   

16.
The Saharan Mineral Dust Experiment (SAMUM) was conducted in May and June 2006 in Tinfou, Morocco. A H-TDMA system and a H-DMA-APS system were used to obtain hygroscopic properties of mineral dust particles at 85% RH. Dynamic shape factors of 1.11, 1.19 and 1.25 were determined for the volume equivalent diameters 720, 840 and 960 nm, respectively.
During a dust event, the hydrophobic number fraction of 250 and 350 nm particles increased significantly from 30 and 65% to 53 and 75%, respectively, indicating that mineral dust particles can be as small as 200 nm in diameter. Log-normal functions for mineral dust number size distributions were obtained from total particle number size distributions and fractions of hydrophobic particles. The geometric mean diameter for Saharan dust particles was 715 nm during the dust event and 570 nm for the Saharan background aerosol.
Measurements of hygroscopic growth showed that the Saharan aerosol consists of an anthropogenic fraction (predominantly non natural sulphate and carbonaceous particles) and of mineral dust particles. Hygroscopic growth and hysteresis curve measurements of the 'more' hygroscopic particle fraction indicated ammonium sulphate as a main component of the anthropogenic aerosol. Particles larger than 720 nm in diameter were completely hydrophobic meaning that mineral dust particles are not hygroscopic.  相似文献   

17.
The Aerodyne aerosol mass spectrometer (Q-AMS) was coupled with a counterflow virtual impactor (CVI) for the first time to measure cloud droplet residuals of warm tropospheric clouds on Mt. Åreskutan in central Sweden in July 2003. Operating the CVI in different operational modes generated mass concentration and species-resolved mass distribution data for non-refractory species of the ambient, interstitial, and residual aerosol. The ambient aerosol measurements revealed that the aerosol at the site was mainly influenced by long-range transport and regional photochemical generation of nitrate and organic aerosol components. Four different major air masses were identified for the time interval of the experiment. While two air masses that approached the site from northeastern Europe via Finland showed very similar aerosol composition, the other two air masses from polar regions and the British Islands had a significantly different composition. During cloud events the larger aerosol particles were found to be activated into cloud droplets. On a mass basis the activation cut-off diameter was approximately 150 nm for nitrate and organics dominated particles and 200 nm for sulfate dominated particles. Generally nitrate and organics were found to be activated into cloud droplets with higher efficiency than sulfate. While a significant fraction of the nitrate in ambient particles was organic nitrates or nitrogen-containing organic species, the nitrate found in the cloud droplet residuals was mainly ammonium nitrate. After passage of clouds the ambient aerosol size distribution had shifted to smaller particle sizes due to the predominantly activation of larger aerosol particles without a significant change in the relative composition of the ambient aerosol.  相似文献   

18.
西安市一次晴空气溶胶粒子的观测分析   总被引：17，自引：0，他引：17  
何绍钦 《气象》1987,13(5):19-22
1982年夏季,我国第一架装有PMS粒子测量系统的气象科研考察飞机在西安市首次进行大气物理科学考察。本文仅对6月8日西安城市晴天大气气溶胶粒子观测。资料进行了初步分析。结果表明:西安市晴天气溶胶粒子(直径0.5-8μm)浓度值范围在4×10~0-3.8×10~1个/cm~3,分布趋势随高度递减,逆温层对粒子垂直输送有阻滞作用。同时对气溶胶粒子谱分布及谱分布函数作了探讨,并对一些参数进行理论计算。  相似文献   

19.
Size-segregated aerosol samples were collected with a low-pressure impactor (LPI) at urban, roadside and rural sites in winter in Beijing. The size distribution of Polycyclic Aromatic Hydrocarbons (PAHs), organic carbon (OC) and elemental carbon (EC) were measured and this study focused on their size distributions and relationships of PAH to OC/EC. All PAHs show uni-modal at the accumulation mode (0.1–1.8 μm) and almost all PAHs are associated with fine particles. The absence of PAHs in the nucleus mode contributes to the coagulation under the condition of high concentration of the accumulation mode particles. The absence of PAHs in the coarse mode was probably attributed to the low temperature that restrained the redistribution of PAHs from the accumulation mode to the coarse mode. Flu(fluoranthene) and Pyr(pyrene, 4-ring) were the most abundant particulate PAHs ; however, IcdP(indeno[1,2,3-cd]pyrene) and BghiP(benzo[ghi]perylene, 6-ring) were rather low. Diagnostic ratios show vehicle and coal burning were the major sources of PAHs in winter. Ratios at rural site are obviously different from those found at roadside and urban sites. Lower value of OC/EC in the rural area than that in the urban area was probably resulted from coal burning prevailed in the rural area. OC1 and OC2 exhibit uni-mode distribution similar to their particle surface area distribution indicating their existence on particles by adsorption. OC3 and OC4 show bi-mode distribution. Grinding of biomass debris can be a probable source of OC3 and OC4 in the coarse mode. EC1 is mostly from the pyrolysis of OC; however, both the natural and anthropogenic emissions contribute to EC2. The correlation between size-segregated PAHs and carbonaceous component is also discussed to identify their sources.  相似文献   

20.
An Aerodyne quadruple aerosol mass spectrometer (Q-AMS) has been used to provide on-line measurements of size dependent chemical composition of fine aerosol particles (PM1) at the Air Pollution Research Station in Preila, Lithuania, representing the east Baltic region. The size dependent chemical composition measurements by AMS have revealed that in marine air masses 118?nm mode organics-containing particles were fresher compared to sulfate-containing particles (295?nm), likely originated as secondary aerosol from forest emissions or produced by primary sea spray over the Baltic Sea. In polluted continental air masses sulfate and organics were highly internally mixed and aged. The mass spectral results indicated that the major components of organic compounds were oxygenated organic species with strong signals at m/z 18, 43, 44 with several specific features. Positive matrix factorization (PMF) of AMS organic mass spectral data has identified three factors: aged oxygenated low-volatility organic aerosol (LV-OOA), less oxygenated semi-volatile organic aerosol (SV-OOA), and biogenic organic aerosol (BGOA) of either terrestrial or marine origin. The measurements were compared with a real-time particulate matter Beta Absorption Monitor (Thermo ESM Andersen) and Micro Orifice Uniform Deposit Impactor (MOUDI) data. The intercomparison showed a good correlation and a stable ratio between PM1 and PM2.5 concentrations. A comparison of the on-line Q-AMS data and the off-line MOUDI fine particle (<1???m) data yielded a reasonable agreement in size distributions but not the absolute mass concentrations due to sampling conditions, evaporation of acidic species from sampling substrates and bounce of the particles in the MOUDI.  相似文献   

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