Real-Time Observation on Water-Soluble Ions of PM_(2.5)in Beijing under the Influences of Different Air Masses in Summer

To further understand the variations of water-soluble ions in PM2.5 in Beijing,the authors observed their concentrations continuously and in high temporal resolution by the system for rapid collection of fine particles and ion chromatography(RCFP-IC) during 12–18 July 2010.These results combined with those of earlier backward trajectory research are used analyzed to determine the causes of concentration changes in water-soluble ions under the influences of two kinds of air masses in summer.The results indicate that concentrations of NO3-,SO42-,and NH4+ were influenced strongly by the continental air mass than by the marine air mass.Cl- and Na+ were not changed significantly.Because the sources of K+,Mg2+,and Ca2+ are mainly concentrated on land,their concentration levels were slightly higher under the control of continental air mass than that of the marine air mass.Variations of NO2- during the observation differed from those of other ions;its concentration was significantly higher under the influence of marine air mass.Moreover,the authors obtain the diurnal variations of eight water-soluble inorganic ions including NH4+,K+,Mg2+,Ca2+,Cl-,NO2-,NO3-,and SO42-.Diurnal variations of NH4+,NO3-,and Cl- showed single peak,which appeared before noon,while SO42- showed two peaks that appeared during rush hours.Those of Mg2+,Ca2+,and K+ showed single peak that appeared in the afternoon.That of NO2- showed with a peak appearing at sunrise and a valley appearing at sunset.     

湛江地区一次冷锋型海雾微物理特征

利用2010年3月31日—4月2日冷锋天气系统影响下湛江海雾综合观测资料,分析了海雾的微物理特征及海雾过程中气溶胶粒子谱的演变特征。结果表明,海雾的生消与风场密切相关,海雾生成和发展与较强的ESE气流相联系,而弱的NE气流则会促使海雾减弱或消散。湛江海雾的雾滴数浓度为100~102cm-3,液态含水量为0.001~0.232 g·m-3,雾滴平均半径小于10μm,雾滴峰值半径多位于1.4μm。海雾雾滴谱分布以单调递减谱为主,谱宽超过20μm,且雾发展过程中雾滴谱谱宽存在突然增宽和迅速减小的现象。海雾过程中雾滴数浓度的变化主要是由半径小于5μm的雾滴数密度变化引起的。海雾过程对气溶胶粒子的湿清除效果并不显著,雾过程中粒径小于0.1μm和大于4μm的气溶胶粒子数密度显著减少,但在雾消散后又迅速恢复到雾发生前的水平。     

The Role of the Aerosol Indirect Effect in the Northern Indian Ocean Warming Simulated by CMIP5 Models

The northern Indian Ocean （NIO） experienced a decadal-scale persistent warming from 1950 to 2000, which has influenced both regional and global climate. Because the NIO is a region susceptible to aerosols emis- sion changes, and there are still large uncertainties in the representation of the aerosol indirect effect （ALE） in CMIP5 （Coupled Model Intercomparison Project Phase 5） models, it is necessary to investigate the role of the AIE in the NIO warming simulated by these models. In this study, the authors select seven CMIP5 models with both the aerosol direct and indirect effects to investigate their performance in simulating the basin-wide decadal-scale NIO warming. The results show that the decreasing trend of the downwelling shortwave flux （FSDS） at the surface has the major damping effect on the SST increasing trend, which counteracts the warming effect of greenhouse gases （GHGs）. The FSDS decreasing trend is mostly contrib- uted by the decreasing trend of cloudy-sky surface downwelling shortwave flux （FSDSCL）, a metric used to measure the strength of the AIE, and partly by the clear-sky surface downwelling shortwave flux （FSDSC）. Models with a relatively weaker AIE can simulate well the SST increasing trend, as compared to observation. In contrast, models with a relatively stronger AIE produce a much smaller magnitude of the increasing trend, indicat- ing that the strength of the AIE in these models may be overestimated in the NIO.     

对流层气溶胶的直接气候效应对平流层的影响

通过WACCM-3模式中气溶胶光学厚度与卫星资料的对比发现,模式可以很好地再现全球气溶胶的主要分布特征,但在一些区域还存在数值上的差异。利用数值试验研究对流层气溶胶的直接气候效应对平流层气候的影响,结果表明:对流层气溶胶对平流层气候有明显影响,平流层化学过程在这一影响中起重要作用,而对流层气溶胶对平流层辐射的影响不是其直接气候效应对平流层影响的主要原因。其机制可能是对流层气溶胶改变对流层的辐射平衡,影响对流层的温度和大气环流,进而影响行星波的上传,使得平流层气候发生变化;影响区域主要位于高纬度和极地地区,南半球的变化比北半球大,温度变化最大达10 K,纬向风变化最大可达12 m/s,臭氧体积分数最多减少0.8×10-6。     

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.     

A Review of Aerosol Optical Properties and Radiative Effects

Atmospheric aerosols influence the earth's radiative balance directly through scattering and absorbing solar radiation, and indirectly through affecting cloud properties. An understanding of aerosol optical properties is fundamental to studies of aerosol effects on climate. Although many such studies have been undertaken, large uncertainties in describing aerosol optical characteristics remain, especially regarding the absorption properties of different aerosols. Aerosol radiative effects are considered as either positive or negative perturbations to the radiation balance, and they include direct, indirect (albedo effect and cloud lifetime effect), and semi-direct effects. The total direct effect of anthropogenic aerosols is negative (cooling), although some components may contribute a positive effect (warming). Both the albedo effect and cloud lifetime effect cool the atmosphere by increasing cloud optical depth and cloud cover, respectively. Absorbing aerosols, such as carbonaceous aerosols and dust, exert a positive forcing at the top of atmosphere and a negative forcing at the surface, and they can directly warm the atmosphere. Internally mixed black carbon aerosols produce a stronger warming effect than externally mixed black carbon particles do. The semi-direct effect of absorbing aerosols could amplify this warming effect. Based on observational (ground-and satellite-based) and simulation studies, this paper reviews current progress in research regarding the optical properties and radiative effects of aerosols and also discusses several important issues to be addressed in future studies.     

A global satellite view of the seasonal distribution of mineral dust and its correlation with atmospheric circulation

Aerosols make a considerable contribution to the climate system through their radiative and cloud condensation nuclei effects, which underlines the need for understanding the origin of aerosols and their transport pathways. Seasonal distribution of mineral dust around the globe and its correlation with atmospheric circulation is investigated using satellite data, and meteorological data from ECMWF. The most important sources of dust are located in North Africa, the Middle East and Southwest Asia with an observed summer maximum, and East Asia with a spring peak. Maximum dust activity over North Africa and the Middle East in summer is attributed to dry convection associated with the summertime low-pressure system, while unstable weather and dry conditions are responsible for the spring peak in dust emission in East Asia. Intercontinental transport of mineral dust by atmospheric circulation has been observed, including trans-Atlantic transport of North African dust, trans-Pacific transport of Asian dust, and transport of dust from the Middle East across the Indian Ocean. The extent of African dust over the Atlantic Ocean and its latitudinal variation with season is related to the large-scale atmospheric circulation, including seasonal changes in the position of the intertropical convergence zone (ITCZ) and variation of wind patterns. North African aerosols extend over longer distances across the North Atlantic in summer because of greater dust emission, an intensified easterly low level jet (LLJ) and strengthening of the Azores-Bermuda anticyclonic circulation. Transport of East Asian aerosol is facilitated by the existence of a LLJ that extends from East Asia to the west coast of North America.     

东亚季风区近地面大气气溶胶中OCPs和PCBs纬度分布：以7Be为参照系

连续一年在北京、青岛、广州以每周3d的时间尺度同步采集近地面大气中气溶胶中7Be的测定数据以及在春、秋季节变换时期我国5个不同纬度城市大气气溶胶中7Be和典型持久性有机污染物（有机氯农药和多氯联苯1的同步观测数据,并对文献上发表的我国其他城市近地面大气中气溶胶中’Be年平均值数据进行了分析。通过对以上数据资料的总结和分析,观察到在东亚季风区近地表大气气溶胶中7Be浓度的年平均值呈现正态分布模式,并且在中纬度北纬40°N附近达到极大值。大气气溶胶中7Be在春、秋季节变换时期我国不同纬度城市的瞬时纬度分布仍呈现正态分布模式,但以30°N为最大值。在秋季大气颗粒相中HCHs和PCBs浓度最大值出现在30°N。气相中PCB-28所占百分比随纬度增高而增大,而颗粒相中PCB-28的纬度变化不大。蒸汽压较低的PCB-180在气相中的浓度基本上不随纬度变化,而颗粒相中PCB-180则基本上集中在纬度36。N左右,表明在东亚季风区大气中挥发性较低的POPs化合物具有某种纬度聚焦作用。以宇宙射线成因核素7Be作为大气环流的参照系,可以得出东亚季风区大气环流可影响持久性有机污染物纬度分布的结论。     

乌鲁木齐冬季黑碳气溶胶污染特征初步研究

利用2010年2月乌鲁木齐大气成分观测站黒碳仪观测数据,结合散射系数及常规观测资料,对乌鲁木齐冬季黑碳气溶胶浓度变化特征进行了分析,并通过气流后向轨迹进行了来源分析。结果表明：(1)观测期间BC质量浓度日平均值为12707±4673 ng.m-3,浓度变化范围为4916~22997 ng.m-3,散射系数日均值为1086±561Mm-1,变化范围为350~2232 Mm-1。BC质量浓度和散射系数日均值变化趋势基本一致;(2)BC质量浓度日变化具有明显的峰值和谷值,峰值分别出现在9~11时和20~22时,谷值分别出现在4~6时和16~18时,散射系数与BC质量浓度日变化趋势基本一致,相对其有一定的滞后。春节期间燃放烟花爆竹对空气污染物浓度上升有明显作用,显著影响BC质量浓度日变化规律;(3)乌鲁木齐冬季大气层结稳定,污染物不易扩散,风速和降水对黑碳气溶胶浓度具有明显的稀释作用。在乌鲁木齐特殊的地形和气象条件下,本地源排放与来自周边城市群污染物输送的叠加使得污染更加严重。     

青藏高原黑碳气溶胶传输及沉降的季节特征模拟分析

根据全球气溶胶气候模式GEM-AQ/EC的1995~2004年模拟,分析了青藏高原大气黑碳气溶胶的来源、传输及沉降季节特征。研究表明:青藏高原黑碳气溶胶主要来自自由对流层和大气边界层的输送。相对于自由对流层的黑碳输送,紧邻青藏高原的南亚、东亚以及东南亚大气边界层的输送更有效,它形成了青藏高原由北向南、自西往东黑碳气溶胶浓度和沉降明显递增的基本分布形态。横跨欧亚大陆自由对流层的黑碳气溶胶由西向东向青藏高原的输送全年不变,夏季输送路径最北但强度最弱,冬季路径最南而强度最强。大气边界层黑碳气溶胶的输送受控于亚洲季风环流变化,来自南亚的黑碳气溶胶在春季越过孟加拉湾传输进入高原东南部,夏季则可翻越喜马拉雅山抵达青藏高原南部腹地;同时我国中部排放的黑碳气溶胶也在东亚夏季风向北扩展中驱动它从东向西往青藏高原东北部传输。从秋季到冬季,随着夏季风撤退,南亚黑碳源区向青藏高原传输衰退,东亚冬季风的反气旋性环流的南侧及西南侧的偏东风携带秋季我国东南部源区和冬季东南亚源区黑碳气溶胶向青藏高原东南部传输。受青藏高原明显的暖湿季和干冷季气候影响,干湿沉降分别主导了青藏高原冬季和夏季黑碳沉降,夏季青藏高原黑碳气溶胶沉降总量大多超过8~10 kg·km-2,在高原东北部的最高值超过40 kg·km-2。冬季青藏高原黑碳气溶胶沉降量最低,大部地区黑碳沉降低于5 kg·km-2。青藏高原黑碳沉降的冬夏季节相差约为2~8倍。