北京上甸子秋冬季大气气溶胶的散射特征

分析了北京上甸子秋冬季气溶胶散射系数的变化特征、散射系数与PM2.5质量浓度的关系, 结合气象资料分析了风场对气溶胶散射系数变化的影响。通过研究得出, 上甸子秋冬季气溶胶散射系数平均值和标准差分别为179.7 Mm-1和253.2 Mm-1；阴天条件下的散射系数明显高于晴天；散射系数与PM2.5质量浓度之间有较好的相关性, 其相关系数为0.93；此外, 由于上甸子特殊的地理位置, 风场对气溶胶散射系数的影响显著, 不同风向条件下气溶胶散射系数差别很大。     

Macro-and Micro-Structures of Heavy Fogs and Visibility in the Dayaoshan Expressway

Belonging to the southern subtropical moist type of monsoon climate,the Nanling mountainous area experiences heavy fogs whenever quasi-stationary fronts appear there from September to May.There can be as many as 15-18 days of heavy fogs per month.Fogs have more serious consequences in the Lechang-Ruyuan section of the Beijing-Zhuhai Expressway(the longest expressway in China)that passes through the main part of the Nanling Mts.,where the road rises from 200m to more than 800m above sea level(ASL).For a major motorway in the mountainous areas of Nanling Mts.,two multidisciplinary integrated field observations were carried out,which measured visibility by the naked eyes,visibility by instrument,spectrum of fog- drops,liquid water content(LWC)of fog,tethered sounding,dual-parameter low-level sounding,turbulence diffusion within fog layers,aerosol spectra of size and composition,sampled fog water compositions,and sampled rainwater compositions.Typical cases were probed for their analyses of synoptics,micro- and macro-structures and microphysics.It is understood that heavy fogs take place with high frequency in the area and bring about serious consequences.Being typical advection and upslope fogs,they are in essence low-lying clouds appearing at high altitudes,which are closely related with the activity of South China frontal processes,especially the South China quasi-stationary fronts,and reflect on the role of local terrain as well.The heavy fogs are characteristic of long duration,extremely low visibility,well-organized lump- shaped structure,large-size fog-drops,moderate concentration,high LWC,and stronger turbulent diffusion within the fog layers than in fine sky.They differ much from radiation fogs,which are better documented in previous study in China.It is found that fog LWC is in significant anti-correlation with visibility so that large LWC is associated with small visual range.It is also noted that one of the reasons for the fluctuation of characteristic quantities of micro-structure such as the LWC of fog in the area is,in addition to the inhomogeneous structure of the fog itself,the effect of advection and inhomogeneous underlying surface; during the translation of fog with the ambient wind,irregular upslope and cross-over movement is another reason for the inhomogeneous structure and fluctuation of fog.The spectrum of the aerosol size displays itself as the power function of monotonous descent.The concentration of submicrometer particles is even higher.The high-concentration sulfate particles found in the aerosols of Nanling Mts.are actually good nuclei for condensation,which are favorable for the formation of fog.The presence of fog can help cleanse the trace compositions in the atmosphere so that fog droplets contain high levels of polluting elements.In the meantime,compared to cloud droplets,fog droplets are easier to be captured by the vertical surfaces of objects on the land surface,such as vegetation and buildings to constitute another kird of cleansing process. In vast stretches of forest like the Nanling Mts.,this kind of cleansing may be quite important.Studying the characteristic variation of fogs in the area realistically assists in setting up a forecast and warning system for local fogs and provides basic information for fog dispersal experiments.     

Elemental Composition of Mineral Aerosol Generated from Sudan Sahara Sand

Eighteen soil samples from central Sudan were fractionated by dry sieving ina size fraction from <45 m to >300 m while aerosols generatedfrom these soils were fractionated in the particle size range from 0.25 mto >16 m. The elemental concentrations of soil samples were determinedby energy-dispersive X-ray fluorescence, while the elemental concentrationsof generated aerosols were analysed by particle-induced X-ray emission. Theelements Al, K and Rb show a slight positive fractionation with decreasingparticle size throughout the particle size range studied. The concentrationsof Ca, Mn, Fe, Sr and Y are maximum in the small soil size fraction (<45m) and decrease for the coarse soil size fractions, while in the mineralaerosol particle sizes (0.25– > 16 m) the concentrations remainmore or less constant. The size distributions for Cr, Ti and Zr show a maximumin the particle size range 45–100 m and the concentrations of theseelements decrease sharply in the aerosol fraction down to 16 m to remainconstant in the smaller aerosol fractions.Enrichment factors for the elements were calculated relative to five referencematerials: average crustal rock, average soil, the investigated Sahara bulksoil, the finest fraction of this soil and the aerosol generated from thissoil, and using four reference elements: Al, Si, Ti and Fe. The enrichmentfactors were found to vary significantly depending on the choice of thereference material or the reference element. The enrichment factors for theSudan mineral aerosol were almost identical to those for Khartoum atmosphericaerosol but different from those for Namib mineral aerosol and Israelatmospheric aerosol following dust storms. Multivariate display methods(cluster analysis, principal component analysis and linear discriminantanalysis) were applied to the element ratios in the mineral aerosol from theSahara and Namib and this showed that these mineral aerosol can bedifferentiated into different groups. An attempt was also made to relate themineral aerosol to its parent soil through the use of these multivariatetechniques and the elemental ratios in both the mineral aerosols and the bulksoils (Namib and Sahara). It was also possible using the elemental ratios andthe multivariate display methods to associate the crustal component to themineral aerosol generated from the Sahara.     

Single Particle Analysis of Aerosols, Observed in the Marine Boundary Layer during the Monterey Area Ship Tracks Experiment (MAST), with Respect to Cloud Droplet Formation

The chemical composition of individual particles >0.2 m sampled duringthe MAST-experiment wereanalysed by SEM-EDX, in combination with multivariatetechniques. The objective of this experiment was toidentify the mechanisms responsible for themodification of marine stratocumulus clouds byemissions from ships and in a wider sense to provideinformation on the global processes involved inatmospheric modification of cloud albedo. Aerosolswere examined under different MBL pollution levels(clean, intermediately polluted and moderatelypolluted) in five different reservoirs: backgroundbelow-cloud and above-cloud aerosol; background clouddroplet residual particles; below-cloud ship plumeaerosol and ship track cloud droplet residualparticles.In this study a relation was provided between theaerosol emitted from the ship's stack to an effect incloud. Additionally, a large fraction of the ambientaerosol was found to be composed of organic materialor other compounds, consisting of low Z-elements,associated with chlorine. Their number fraction waslargest in clean marine boundary layers, and decreasedwith increasing pollution levels. The fraction of`transformed sea salt' (Na, Cl, S), on the other hand,increased with the pollution level in the MBL. Only20% of the particles fell within the detectable rangeof the analysis.     

Letter to the editor A strange cloud in the Arctic summer stratosphere 1998 above Esrange (68°N), Sweden

When the University of Bonn lidar on the Esrange (68°N, 21°E), Sweden, was switched on in the evening of July 18, 1998, a geometrically and optically thin cloud layer was present near 14 km altitude or 400 K potential temperature, where it persisted for two hours. The tropopause altitude was 4 km below the cloud altitude. The cloud particles depolarized the lidar returns, thus must they have been aspherical and hence solid. Atmospheric temperatures near 230 K were approximately 40 K too high to support ice particles at stratospheric water vapour pressures of a few ppmv. The isentropic back trajectory on 400 K showed the air parcels to have stayed clear of active major rocket launch sites. The air parcels at 400 K had travelled from the Aleutians across Canada and the Atlantic Ocean arriving above central Europe and then turned northward to pass over above the lidar station. Parcels at levels at ±25 K from 400 K had come from the pole and joined the 400 K trajectory path above eastern Canada. Apparently the cloud existed in a filament of air with an origin different from those filaments both above and below. Possibly the 400 K level air parcels had carried soot particles from forest wild fires in northern Canada or volcanic ash from the eruption of the Korovin Volcano in the Aleutian Islands.     

Controls of dimethyl sulphide in the Bay of Bengal during BOBMEX-Pilot cruise 1998

The air-sea exchange is one of the main mechanisms maintaining the abundances of trace gases in the atmosphere. Some of these, such as carbon dioxide and dimethyl sulphide (DMS), will have a bearing on the atmospheric heat budget. While the former facilitates the trapping of radiation (greenhouse effect) the latter works in the opposite direction through reflectance of radiation back into space by sulphate aerosols that form from oxidation of DMS in atmosphere. Here we report on the first measurements made on DMS in the Bay of Bengal and the factors regulating its abundance in seawater. Phytoplankton alone does not seem to control the extent of DMS concentrations. We find that changes in salinity could effectively regulate the extent of DMSP production by marine phytoplankton. In addition, we provide the first ever evidence to the occurrence of DMS precursor, DMSP, in marine aerosols collected in the boundary layer. This suggests that the marine aerosol transport of DMSP will supplement DMS gaseous evasion in maintaining the atmospheric non-sea salt sulphur budget.     

2009年石家庄地区大气气溶胶的飞机探测研究

利用2009年石家庄地区不同季节的3次机载粒子探测系统PMS(Particle Measurement System)的探测资料,结合地面天气形势、风场和探空资料对石家庄地区,晴空背景下大气气溶胶的统计特征、数浓度、平均粒径的垂直分布特征以及谱分布特征进行了分析。结果表明:晴天条件下气溶胶的数浓度随高度递减,粒径随高度变化不大;在数值上,4月16日气溶胶数浓度和粒径最大,其次是10月15日,最小的是6月10日,3次粒径变化幅度都不大;逆温层底层气溶胶明显积累,气溶胶浓度在1.5 km以下大气边界层内明显高于其他层次,逆温层的高度和厚度影响气溶胶的分布;3次不同季节晴天背景下石家庄地区气溶胶谱型基本一致呈单峰分布,小于0.3μm的细粒子对气溶胶的数浓度贡献最大。     

Numerical Study of the Effect of Anthropogenic Aerosols on Spring Persistent Rain over Eastern China

The eff ect of anthropogenic aerosols on the spring persistent rain （SPR） over eastern China is investigated by using a high-resolution Community Atmosphere Model version 5.1 （CAM5.1）. The results show that the SPR starts later due to anthropogenic aerosols, with a shortened duration and reduced rainfall amount. A reduction in air temperature over the low latitudes in East Asia is linked to anthropogenic aerosols;so is a weakened southwesterly on the north side of the subtropical high. Meanwhile, air temperature increases signifi cantly over the high latitudes. This north-south asymmetrical thermal eff ect acts to reduce the meridional temperature gradient, weakening the upper-level westerly jet over East Asia and the vertical motion over southeastern China. As a result, the SPR is reduced and has a much shorter duration. The indirect eff ect of anthropogenic aerosols also plays an important role in changing the SPR. Cloud droplet number concentration increases due to anthropogenic aerosols acting as cloud condensation nuclei, leading to a reduction in cloud eff ective radius over eastern China and a reduced precipitation effi ciency there.     

Impact of Direct Radiative Forcing of Anthropogenic Aerosols on Diurnal Temperature Range in January in Eastern China

This study investigates the changes in January diurnal temperature range(DTR) in China during 1961-2000.The observed DTR changes during 1981-2000 relative to 1961-80 are first analyzed based on the daily temperature data at 546 weather stations.These observed DTR changes are classified into six cases depending on the changes in daily maximum and minimum temperatures,and then the occurrence frequency and magnitude of DTR change in each case are presented.Three transient simulations are then performed to understand the impact of greenhouse gases(GHGs) and aerosol direct forcing on DTR change:one without anthropogenic radiative forcing,one with anthropogenic GHGs,and another one with the combined forcing of GHGs and five species of anthropogenic aerosols.The predicted daily DTR changes during the years 1981-2000 are also classified into six cases and are compared with the observations.Results show that the previously proposed reason for DTR reduction,a stronger nocturnal warming than a daytime warming,explains only 19.8%of the observed DTR reduction days.DTR reductions are found to generally occur in northeastern China,coinciding with significant regional warming.The simulation with GHG forcing alone reproduces this type of DTR reduction with an occurrence frequency of 32.9%,which is larger than the observed value.Aerosol direct forcing reduces DTR mainly by daytime cooling.Consideration of aerosol cooling improves the simulation of occurrence frequencies of different types of DTR changes as compared to the simulation with GHGs alone,but it cannot improve the prediction of the magnitude of DTR changes.     

全球和亚洲人为气溶胶影响东亚气候的数值模拟研究

利用海气耦合的全球气候模式CSIRO-Mk3.6分析比较了全球和亚洲人为气溶胶对东亚各季节气候的不同影响。结果表明,全球和亚洲外人为气溶胶使得东亚地区年平均地表温度分别下降0.9℃和0.55℃。亚洲区域气溶胶强迫决定了东亚近地面降温的时空分布特征,而亚洲区域外气溶胶进一步增强了我国北方夏季的近地面降温。各个季节对流层中上层的降温主要受区域外气溶胶的影响,并引起东亚高空急流强度和位置的变化,造成夏季和秋季明显的经向环流异常。同时,亚洲气溶胶影响各季节东亚低层环流场的响应,使得东亚陆地降水减少,而区域外气溶胶则主要影响冬季中高纬度和夏、秋季南海地区的低层风场。总体上,亚洲区域内、外人为气溶胶会增强我国冬、夏季风低层环流,并共同决定南海地区的降水变化。