Cloud condensation nuclei spectra derived from size distributions and hygroscopic properties of the aerosol in coastal south-west Portugal during ACE-2

In this work we propose and test a method to calculate cloud condensation nuclei (CCN) spectra based on aerosol number size distributions and hygroscopic growth factors. Sensitivity studies show that this method can be used in a wide variety of conditions except when the aerosol consist mainly of organic compounds. One crucial step in the calculations, estimating soluble ions in an aerosol particle based on hygroscopic growth factors, is tested in an internal hygroscopic consistency study. The results show that during the second Aerosol Characterization Experiment (ACE-2) the number concentration of inorganic ions analyzed in impactor samples could be reproduced from measured growth factors within the measurement uncertainties at the measurement site in Sagres, Portugal.
CCN spectra were calculated based on data from the ACE-2 field experiment at the Sagres site. The calculations overestimate measured CCN spectra on average by approximately 30%, which is comparable to the uncertainties in measurements and calculations at supersaturations below 0.5%. The calculated CCN spectra were averaged over time periods when Sagres received clean air masses and air masses influenced by aged and recent pollution. Pollution outbreaks enhance the CCN concentrations at supersaturations near 0.2% by a factor of 3 (aged pollution) to 5 (recent pollution) compared to the clean marine background concentrations. In polluted air masses, the shape of the CCN spectra changes. The clean spectra can be approximated by a power function, whereas the polluted spectra are better approximated by an error function.     

基于航测的珠三角气溶胶垂直分布及活化特性

2017年9月14—27日在珠江三角洲地区开展了6个架次飞机观测试验。利用飞行获取的气溶胶、云凝结核、云滴及常规气象探头观测资料,结合天气形势、气象条件及气团后向轨迹分析,研究了珠江三角洲地区深圳气溶胶数浓度及其谱的垂直分布特征,配合不同过饱和度条件下云凝结核浓度观测,分析了气溶胶活化特性。结果表明:在不同天气条件下,深圳低层气溶胶数浓度变化范围为500~9000 cm-3;边界层内气溶胶分布相对均匀,谱型随高度变化与气象条件相关。将6个架次气溶胶观测资料根据数浓度及谱型分为3种类型:类型Ⅰ为海洋型气溶胶,数浓度小,粒子尺度大,谱型呈双峰分布;类型Ⅲ为大陆型气溶胶,数浓度高,粒子尺度小,谱宽较宽且呈三峰分布;类型Ⅱ为海洋大陆影响型气溶胶,即受海洋和大陆共同影响,数浓度低于类型Ⅲ高于类型Ⅰ,谱型为双峰分布。拟合了包含海洋型及大陆型气溶胶的3个架次近地面云凝结核活化谱,计算了气溶胶在不同过饱和度条件下的活化效率。     

Cloud condensation nuclei from biomass burning during the Amazonian dry-to-wet transition season

Aircraft measurements of cloud condensation nuclei (CCN) during the Large-Scale Biosphere–Atmosphere Experiment in Amazonia (LBA) were conducted over the Southwestern Amazon region in September–October 2002, to emphasize the dry-to-wet transition season. The CCN concentrations were measured for values within the range 0.1–1.0% of supersaturation. The CCN concentration inside the boundary layer revealed a general decreasing trend during the transition from the end of the dry season to the onset of the wet season. Clean and polluted areas showed large differences. The differences were not so strong at high levels in the troposphere and there was evidence supporting the semi-direct aerosol effect in suppressing convection through the evaporation of clouds by aerosol absorption. The measurements also showed a diurnal cycle following biomass burning activity. Although biomass burning was the most important source of CCN, it was seen as a source of relatively efficient CCN, since the increase was significant only at high supersaturations.     

Cloud Condensation Nuclei over the Bay of Bengal during the Indian Summer Monsoon

The first measurements of cloud condensation nuclei(CCN) at five supersaturations were carried out onboard the research vessel "Sagar Kanya"(cruise SK-296) from the south to the head-bay of the Bay of Bengal as part of the Continental Tropical Convergence Zone(CTCZ) Project during the Indian summer monsoon of 2012. In this paper, we assess the diurnal variation in CCN distributions at supersaturations from 0.2% to 1%(in steps of 0.2%) and the power-law fit at supersaturation of 1%.The diurnal pattern shows peaks in CCN concentration(NCCN) at supersaturations from 0.2% to 1% between 0600 and 0700 LST(local standard time, UTC+0530), with relatively low concentrations between 1200 and 1400 LST, followed by a peak at around 1800 LST. The power-law fit for the CCN distribution at different supersaturation levels relates the empirical exponent(k) of supersaturation(%) and the NCCNat a supersaturation of 1%. The NCCNat a supersaturation of 0.4% is observed to vary from 702 cm~(-3) to 1289 cm~(-3), with a mean of 961 ± 161 cm~(-3)(95% confidence interval), representing the CCN activity of marine air masses. Whereas, the mean NCCNof 1628 ± 193 cm~(-3) at a supersaturation of 1% is higher than anticipated for the marine background. When the number of CCN spectra is 1293, the value of k is 0.57 ± 0.03(99% confidence interval)and its probability distribution shows cumulative counts significant at k ≈ 0.55 ± 0.25. The results are found to be better at representing the features of the marine environment(103 cm~(-3) and k ≈ 0.5) and useful for validating CCN closure studies for Indian sea regions.     

Differentiating natural and anthropogenic cloud condensation nuclei in the California coastal zone

Aerosol samples were collected and cloud condensation nuclei (CCN) concentrations at five supersaturations were measured along and off the central California coast within the cloud-topped, marine boundary layer from aircraft flights during August 2007. Receptor modelling has been applied to estimate the natural versus anthropogenic source contribution of cloud condensation nuclei in this region, a region of climatically important marine stratocumulus. The results suggest that anthropogenic CCN accounted for about 50% of the CCN active at 0.3% supersaturation in this region during the measurement period.     

华北中部夏季气溶胶垂直分布及其与云凝结核和云滴转化关系的飞机观测研究

气溶胶的时空分布及其核化成云的转化过程是云降水物理研究的重点,也是气候变化中气溶胶间接效应关注的热点问题。利用2013～2014年期间在华北中部山西地区开展的9架次夏季晴天和积云天气情况下的气溶胶、云凝结核（CCN）及云滴数浓度观测资料,分析研究了气溶胶的垂直分布、谱分布、来源特征及其与云凝结核、云滴数浓度的转化关系。研究结果表明,大气边界层逆温层结对气溶胶、CCN垂直分布有重要影响,不同天气条件下气溶胶谱型在低层差异较大而高层基本一致;垂直方向上CCN数浓度与气溶胶数浓度有较好的相关性,过饱和度0.3%条件下CCN比率（云凝结核/凝结核）与气溶胶有效直径呈线性关系;积云云下气溶胶与云滴的线性拟合方程为y=1.3x?616.3,拟合相关系数为0.96,气溶胶转化为云滴的比率可达到47%。在过饱和度0.3%条件下,云下CCN与云滴的线性拟合方程为y=1.6x?473.8,拟合相关系数也为0.96,CCN转化为云滴的比率可达到69%。     

Aerosol Properties and Their Impacts on Surface CCN at the ARM Southern Great Plains Site during the 2011 Midlatitude Continental Convective Clouds Experiment

Aerosol particles are of particular importance because of their impacts on cloud development and precipitation processes over land and ocean. Aerosol properties as well as meteorological observations from the Department of Energy Atmospheric Radiation Measurement(ARM) platform situated in the Southern Great Plains(SGP) are utilized in this study to illustrate the dependence of continental cloud condensation nuclei(CCN) number concentration(NCCN) on aerosol type and transport pathways. ARM-SGP observations from the 2011 Midlatitude Continental Convective Clouds Experiment field campaign are presented in this study and compared with our previous work during the 2009–10 Clouds, Aerosol, and Precipitation in the Marine Boundary Layer field campaign over the current ARM Eastern North Atlantic site. Northerly winds over the SGP reflect clean, continental conditions with aerosol scattering coefficient(σ_(sp)) values less than 20 Mm~(-1) and NCCNvalues less than 100 cm~(-3). However, southerly winds over the SGP are responsible for the observed moderate to high correlation(R)among aerosol loading(σ_(sp) 60 Mm~(-1)) and NCCN, carbonaceous chemical species(biomass burning smoke), and precipitable water vapor. This suggests a common transport mechanism for smoke aerosols and moisture via the Gulf of Mexico,indicating a strong dependence on air mass type. NASA MERRA~(-2) reanalysis aerosol and chemical data are moderately to highly correlated with surface ARM-SGP data, suggesting that this facility can represent surface aerosol conditions in the SGP, especially during strong aerosol loading events that transport via the Gulf of Mexico. Future long-term investigations will help to understand the seasonal influences of air masses on aerosol, CCN, and cloud properties over land in comparison to over ocean.     

A new three-stage continuous flow CCN-counter

A three-stage vertical-flow thermal gradient vapour diffusion chamber for the fast, continuous measurement of the number concentration of cloud condensation nuclei (CCN) at three different water vapour supersaturations was constructed. CCN are monitored by imaging cloud droplets in the chamber with a CCD-camera. The counting of droplets and the control of all instrumental parameters are computerized. The instrument was calibrated with NaCl-aerosols, and was successfully operated in the field. Data from 2 weeks of field measurements at an island in the North Sea are presented.     

Cloud condensation nuclei (CCN) concentration in the Brazilian northeast semi-arid region: the influence of local circulation

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.     

Investigation of aerosol indirect effects on simulated flash-flood heavy rainfall over Korea

This study investigates aerosol indirect effects on the development of heavy rainfall near Seoul, South Korea, on 12 July 2006, focusing on precipitation amount. The impact of the aerosol concentration on simulated precipitation is evaluated by varying the initial cloud condensation nuclei (CCN) number concentration in the Weather Research and Forecasting (WRF) Double-Moment 6-class (WDM6) microphysics scheme. The simulations are performed under clean, semi-polluted, and polluted conditions. Detailed analysis of the physical processes that are responsible for surface precipitation, including moisture and cloud microphysical budgets shows enhanced ice-phase processes to be the primary driver of increased surface precipitation under the semi-polluted condition. Under the polluted condition, suppressed auto-conversion and the enhanced evaporation of rain cause surface precipitation to decrease. To investigate the role of environmental conditions on precipitation response under different aerosol number concentrations, a set of sensitivity experiments are conducted with a 5?% decrease in relative humidity at the initial time, relative to the base simulations. Results show ice-phase processes having small sensitivity to CCN number concentration, compared with the base simulations. Surface precipitation responds differently to CCN number concentration under the lower humidity initial condition, being greatest under the clean condition, followed by the semi-polluted and polluted conditions.     

巨盐核对云滴活化影响的数值模拟研究

利用包含云凝结核(CCN)与巨核(GCCN)的核化,云滴凝结和碰并增长的分档气块模式模拟研究了不同的CCN数浓度、上升气流速度、CCN中值半径以及云底温度等情况下GCCN对CCN活化的影响,结果表明,在水汽供应相对充足的情况下GCCN对云滴活化数浓度的影响并不明显;而当水汽供应相对不充足时,增加GCCN至1 cm-3的量级以上可以有效减少CCN的活化数浓度.在水汽供应不充分且其他条件相同的情况下,增大CCN的平均直径或是增加云底温度都可以使GCCN对云滴活化的抑制作用增强.对比分析不同的GCCN数浓度对清洁大气和污染大气云底以上300 m高度处粒子谱型的影响可以看出,在水汽供应不充分的条件下加入GCCN,初始时刻CCN的数浓度对GCCN产生的大云滴数目及云滴谱宽的影响较小.在水汽供应相对充足的情况下,GCCN对CCN活化基本没有抑制作用,但此时在高过饱和度峰值下生成的大量小云滴争食水汽,反而导致云滴群凝结增长速度小于水汽供应相对不充足的情况,此时加入的GCCN可以先活化形成大云滴.     

基于MODIS的春、夏季中国近海气溶胶对于云参数的影响差异研究

通过分析中国近海MODIS数据中气溶胶参数与云参数的相互关系,讨论了该区域气溶胶的间接效应及其对于云的可能影响.结果表明,在中国近海,气溶胶具有明显的间接效应,而且由于气溶胶种类和水汽的季节变化,使得气溶胶的间接作用具有很强的时间变化特征.在夏季,由于人为气溶胶占主导,它作为有效的云凝结核,使得气溶胶光学厚度（AOT）分别与云凝结核数（CCN）有正相关、与云滴有效半径（CER）有负相关性、与云光学厚度（COT）也存在着正相关,气溶胶的间接效应明显;在春季,由于沙尘气溶胶盛行,同时沙尘并不是很好的云凝结核,使得气溶胶光学厚度（AOT）分别与云凝结核数（CCN）的正相关减弱、与云滴有效半径（CER）则由夏季的负相关变为正相关、与云光学厚度（COT）存在弱的负相关,气溶胶的间接效应不明显.     

The effect of aerosol representation on cloud microphysical properties in Northeast Asia

This study performed a three-dimensional regional-scale simulation of aerosol and cloud fields using a meso-scale non-hydrostatic model with a bin-based cloud microphysics. The representation of aerosols in the model has been improved to account for more realistic multi-modal size distribution and multiple chemical compositions. Two case studies for shallow stratocumulus over Northeast Asia in March 2005 were conducted with different aerosol conditions to evaluate model performance. Improved condensation nuclei (CN) and cloud condensation nuclei (CCN) are attributable to the newly constructed aerosol size distribution. The simulated results of cloud microphysical properties (cloud droplet effective radius, liquid water path, and optical thickness) with improved CN/CCN number are close to the retrievals from satellite-based observation. The effects of aerosol on the microphysical properties of shallow stratocumulus are investigated by model simulation, in terms of columnar aerosol number concentration. Enhanced aerosol number concentration results in increased liquid water path in humid case, but invariant liquid water path in dry case primarily due to precipitation occurrence. The changes of cloud microphysical properties are more predominant for small aerosol burden than for large aerosol burden with the retarded changes in cloud mass and size due to inactive condensation and collision-coalescence processes. Quantitative evaluation of sensitivity factor between aerosol and cloud microphysical properties indicates a strong aerosol-cloud interaction in Northeast Asian region.     

Cloud condensation nuclei measurements at Mace Head, Ireland, over the period 1994–2002

Analyses of cloud condensation nuclei (CCN) number concentrations (cm^− 3) measured at the Mace Head Atmospheric Research Station, near Carna, County Galway, Ireland, using a DH Associates Model M1 static thermal diffusion cloud chamber over the period from March 1994 to September 2002 are presented in this work. Air masses are defined as being ‘marine’ if they originate from a wind direction of 180–300° and ‘continental’ air masses are defined as originating from a wind direction of 45–135°. Air masses without such filtering were classified as ‘undefined’ air masses. Air masses were found to be dominated by marine sector air, re-affirming Mace Head as a baseline atmospheric research station. CCN levels for specific air masses at Mace Head were found to be comparable with earlier studies both at Mace Head and elsewhere. Monthly averaged clean marine (wind direction of 180–300° and black carbon absorption coefficient < 1.425 Mm^− 1) CCN and marine CCN varied between 15–247 cm^− 3 and 54–670 cm^− 3, respectively. As expected, significant increases in number concentration were found in continentally sourced CCN over that of marine CCN and were found to follow a log-normal distribution significantly tighter than that of clean marine air masses. No significant trend was found for CCN over the 9-year period. While polluted continental air masses showed a slight increase in CCN concentrations over the winter months, most likely due to increased fuel usage and a lower mixed boundary layer, the dominance of marine sector air arriving at Mace Head, which generally consists of background CCN concentrations, reduced seasonal differences for polluted air. Marine air showed a distinct seasonal pattern, with elevated values occurring over the spring and summer seasons. This is thought to be due to enhanced biogenic aerosol production as a result of phytoplankton bloom activity in the North Atlantic.     

The effect of clouds on aerosol growth in the rural atmosphere

Measurements of accumulation mode aerosol in the atmospheric boundary layer under cloudy and cloud-free conditions, and in the lower free troposphere under cloud-free conditions, were conducted over the rural northwest of England. Normalised size distributions in the cloud-free boundary layer (CFBL) and the cloud-free free troposphere (CFFT) exhibited almost identical spectral similarities with both size distributions possessing a concentration peak mode-radius of ≈0.05 μm or less. By comparison, aerosol distributions observed in cloudy air exhibited a distinctive log-normal distribution with mode-radii occurring at ≈0.1 μm concomitant with a local minimum at ≈0.05 μm. The consistent and noticeable difference in spectral features observed between cloudy and cloud-free conditions suggest that a greater amount of gas-to-particle conversion occurs on cloudy days, presumably through in-cloud aqueous phase oxidation processes, leading to larger sized accumulation mode particles. Apart from the distinct difference between cloudy and cloud-free aerosol spectra on cloudy days, aerosol concentration and mass were observed to be significantly enhanced above that of the ambient background in the vicinity of clouds. Volatility analysis during one case of cloud processing indicated an increase in the relative contribution of aerosol mass volatile at temperatures characteristic of sulphuric acid, along with a smaller fraction of more volatile material (possibly nitric acid and/or organic aerosol). Growth-law analysis of possible growth mechanisms point to aqueous phase oxidation of aerosol precursors in cloud droplets as being the only feasible mechanism capable of producing the observed growth. The effect of cloud processing is to alter the cloud condensation nuclei (CCN) supersaturation spectrum in a manner which increases the availability of CCN at lower cloud supersaturations.     

Modeling Marine Stratocumulus with a Detailed Microphysical Scheme

A one-dimensional 3rd-order turbulence closure model with size-resolved microphysics and radiative transfer has been developed for investigating aerosol and cloud interactions of the stratocumulus-topped marine boundary layer. A new method is presented for coupling between the dynamical model and the mierophysical model. This scheme allows the liquid water related correlations to be directly calculated rather than parameterized. On 21 April 2001, a marine stratocumulus was observed by the Caesar aircraft over the west Pacific Rim south of Japan during the 2001 APEX/ACE-Asia field measurements. This cloud is simulated by the model we present here. The model results show that the general features of the stratocumulus-topped marine boundary layer predicted by the model are in agreement with the measurements. A new onboard cloud condensation nuclei (CCN) counter provides not only total CCN number concentration (as the traditional CCN counters do at a certain supersaturation) but also the CCN size distribution information. Using these CCN data, model responses to different CCN initial concentrations are examined. The model results are consistent with both observations and expectations.The numerical results show that the cloud microphysieal properties are changed fundamentally by different initial CCN concentrations but the cloud liquid water content does not differ significantly. Different initial CCN loadings have large impacts on the evolution of cloud microstructure and radiation transfer while they have a modest effect on thermodynamics. Increased CCN concentration leads to significant decrease of cloud effective radius.     

A numerical simulation of the effect of the number concentration of cloud droplets on Typhoon Chanchu

In recent years, an increase in the number of anthropogenic aerosol particles has raised the global mean content of aerosol particles in the atmosphere from that of preindustrial times. The indirect effects of aerosols on weather and climate cannot be ignored. In this paper, the fifth generation Pennsylvania State University (PSU)?CNational Center of Atmospheric Research (NCAR) Nonhydrostatic Mesoscale Model (MM5) is used to simulate Typhoon Chanchu (international designation: 0601), which affected the northwest Pacific. Simulations are conducted in three two-way nested domains with Mercator map projection. The horizontal grid resolutions of the three domains are 27, 9, and 3?km. A period of 60?h is simulated. Surface and rawinsonde conventional observation data and ocean wind data are additionally incorporated into the initialization data. A control (CTL) experiment is run to produce a reasonable forecast. We change the parameter of the cloud condensation nuclei (CCN) concentration (CNP) in the Reisner-2 scheme of the CTL experiment (the default value is 100?cm^?3) to conduct two sensitivity experiments. They are the very clean marine (VCM) CNP experiment (CNP?=?25?cm^?3) and the severe contamination (SC) CNP experiment (CNP?=?1,000?cm^?3). We investigate the effects of the CNP on Typhoon Chanchu by comparing and analyzing the simulation results of the three experiments in terms of the track, intensity, precipitation, vertical structure, and microphysical processes. The main results show that Typhoon Chanchu slightly weakens as the CNP increases. Increasing the CCN to 1,000?cm^?3 results in less graupel, rainwater, and cloud ice but more cloud water. However, the mixing ratio of snow does not distinctly change as the CNP changes. Increasing the CCN leads a rapid decrease in the autoconversion of cloud water to rainwater. There is no autoconversion of cloud water to rainwater in a seriously polluted continental air mass. As the CNP increases, there is more condensation, evaporation, accretion of cloud water by rainwater, and precipitation fallout. Finally, a seriously polluted continental air mass can result in distinctly lower precipitation efficiency.     

华北部分地区云凝结核的观测分析

利用美国DMT公司生产的连续气流单过饱和度云凝结核计数器对华北部分地区地面和空中云凝结核（CCN）进行了观测研究。地面观测结果表明,太原由于污染严重CCN数浓度高于石家庄。CCN数浓度日最大值、日平均值均随过饱和度的增加而增大。CCN数浓度具有明显的日变化特征,与气象因子、人类活动有关。降水对地面CCN具有明显的冲刷作用。利用关系式N=CSk拟合太原地面CCN活化谱,C〉2200cm-3,k〈l,C、k值很高,属于典型的大陆型核谱。飞机观测资料显示,CCN主要来源于地面,数浓度随高度增加明显减少。高空风向发生变化时,长距离气团输送提供CCN二次源。云对CCN有消耗作用,云内CCN比云外明显减少。     

The influence of the organic aerosol component on CCN supersaturation spectra for different aerosol types

Abstract This paper describes the effect of the presence of water-soluble organic compounds (WSOC) in aerosol particles on the aerosol critical supersaturation as defined by the Köhler theory and on cloud condensation nuclei (CCN) number concentration. Taking into account both the soluble mass increase and the surface tension depression due to WSOC, we calculated a substantial decrease of the aerosol critical supersaturation, which results in a large increase in CCN number concentration. CCN supersaturation spectra were computed for three different aerosol types: marine, rural and urban. The increase of CCN number concentration in the presence of WSOC (with respect to the case when only the inorganic aerosol compounds are considered) varies with aerosol type, with an increase up to 13% in the marine case, up to 97% in the rural case, and up to 110% in the urban case, for the supersaturation range typical of atmospheric conditions.     

Observations of Cloud Condensation Nuclei in North China

Using a DMT （Droplet Measurement Technologies） continuous flow streamwise thermal gradient cloud condensation nuclei （CCN） counter mounted on a Cheyenne IIIA aircraft, about 20 flights for aircraft mea- surements of CCN over North China were conducted in the autumn of 2005 and spring of 2006. According to the design for aircraft observation, the method of spiral ascent or descent in the troposphere was used for the vertical measurement of CCN, and some certain levels were chosen for horizontal measurement. The vertical distributions of CCN concentrations show that most CCN particles are concentrated in the low level of troposphere and CCN concentration decreased with height increasing. It suggests that the main source of CCN is from the surface. This result is consistent with former studies during 1983-1985 in China with a static thermal gradient CCN counter. The comparison of vertical observations between polluted rural area near Shijiazhuang and non-polluted rural area near Zhangjiakou shows that there is about five times difference in CCN concentration. But over two polluted cities, Shijiazhuang and Handan, there is no notable difference in CCN concentration. The horizontal flight measurements for penetrating the cumulus clouds experiment show the apparent decrease of CCN in clouds. It confirms that cloud has a definite consumptive effect on CCN particles because some CCN particles can form cloud droplets. The surface measurements of CCN in Shijiazhuang City were made during June-August 2005. The statistical CCN data show the great difference in concentration at the same supersaturation （S） in Shijiazhuang summertime. The minimum CCN concentrations were 584, 808, and 2431 cm-3, and the maximum concentrations were 9495, 16332, and 21812 cm-3 at S=0.1%, 0.3%, and 0.5%, respectively. CCN has a diurnal variation cycle. From 0600 BT, the concentration began to increase and reached the maximum at about noon. Then it generally decreased throughout the afternoon. The reason maybe is related to the onset o