山东地区秋季飞机观测气溶胶特征的初步分析

综合分析了2006年秋季在山东省进行的0.5—8.0μm范围内的大气气溶胶飞机观测的0—4500m气溶胶数浓度垂直分布,初步讨论了气溶胶与温度的关系,并分析了对气溶胶粒子谱的垂直分布情况。结果显示,气溶胶数浓度随高度呈递减趋势,在逆温层附近气溶胶有累计现象;受城市环境的影响,同一区域城市上空或者城市的下风方气溶胶粒子平均浓度都大于上风方;气溶胶粒子谱受不同天气背景的影响,出现不同类型的谱型,随高度的变化,谱型也有很大的变化。     

天空辐射计观测2006年春季北京地区气溶胶光学特性的研究

利用2006年3～5月天空辐射计观测数据反演得到北京地区春季大气气溶胶光学性质参数,包括大气气溶胶光学厚度(0.5μm)、Angstrm指数、单次散射反射比和粒子谱分布特征。结果表明:北京地区春季气溶胶平均光学厚度0.67,Angstrm指数0.54,单次散射比0.88,粒子吸收性质较弱,粒子谱呈双峰形,以粗粒子为主,粗、细模态粒子粒径分别集中在0.17μm和7.7μm左右。相比2004年此次观测期间气溶胶粒径较大,粒子体积浓度较高,散射作用在其消光特性中的比重略有下降。光学厚度日变化呈单峰型,日间单次散射比随时间逐渐递减,Angstrm指数在上午递减趋势明显,午后变得稳定。对同时观测的天空辐射计与CE-318不同波长光学厚度结果进行比较,结果显示两者得到的光学厚度相关性很好,各波长小时平均结果的相对误差小于7%。     

对流层低层晴空大气气溶胶粒子的观测分布

根据1987年冬季人工增雪飞机(机上装有FSSP-100前向散射粒子谱仪)在新疆不同地区获得的大气气溶胶粒子(尺度0.5-8μm)资料,分析研究了对流层低层晴空大气气溶胶粒子的浓度,尺度谱及垂直分布特征.     

黑碳气溶胶光学厚度的全球分布及分析

利用全球气溶胶数据集GADS(Global Aerosol Data Set)计算了冬夏两季黑碳气溶胶质量浓度分布以及在波长0.55μm处的光学厚度、吸收系数和散射系数在全球的分布,并分析了原因。通过分析黑碳气溶胶复折射指数虚部、单次散射反照率、非对称因子、吸收系数、散射系数和消光系数随波长的变化,得出黑碳气溶胶的吸收系数和散射系数在小于0.5μm的短波范围内具有相同的数量级,随着波长的增大,吸收系数比散射系数大几个数量级;黑碳气溶胶对小于1μm的短波有强烈的吸收作用。另外还给出了冬夏两季南北半球及全球黑碳气溶胶平均光学厚度值、7个地区黑碳气溶胶光学厚度及质量浓度最大值,其中冬季黑碳气溶胶光学厚度的最大值为0.027 5,位于东亚地区;而质量浓度最大值为1.555μg/m3,位于西欧地区。     

沙尘气溶胶光学厚度的全球分布及分析

利用全球气溶胶数据GADS(Global Aerosol Data Set)计算了冬夏两季4种类型(积聚型、核型、粗粒型和传输型)沙尘气溶胶0.55μm光学厚度的全球分布。通过分析得出,气溶胶的消光系数和垂直厚度对光学厚度的影响很大。全球沙尘气溶胶分布具有明显的季节和地理差异,4个沙尘暴多发区,分别位于北非、中亚地区、澳大利亚西部和北美西部。中亚地区冬季沙尘气溶胶强度和范围比夏季大,北美和澳大利亚地区则相反,冬季光学厚度最大值位于北非的中部地区,而夏季其最大值位于非洲北部靠近大西洋的地区。沙尘气溶胶对<8μm的辐射吸收作用很弱,散射能力较强;对于>8μm的辐射吸收能力很强,吸收带位主要于8~11μm范围内。     

北京及周边地区2003年夏秋季气溶胶和云滴分布特征

对2003年夏秋季利用机载PMS在北京及周边地区进行的不同天气状况下6次气溶胶粒子探测资料进行了分析.结果表明,北京及周边地区气溶胶粒子的分布,在不同天气背景时有较大差别.粒子平均浓度的最大值为3.46×102cm-3,最大粒子浓度为5.26×103cm-3,相差一个量级;粒子平均最大直径为1.392μm,最大直径为2.75μm.粒子平均浓度的最小值为25.7cm-3.在有雾的天气条件下,气溶胶粒子浓度在近地层基本随高度的增加而减小,粒子尺度变化较为复杂.在阴雨天气情况下,气溶胶粒子浓度和尺度都有增加的现象.另外,逆温层底存在明显的气溶胶粒子累积.0℃层以下气溶胶粒子呈单峰分布,0℃层以上气溶胶出现双峰结构.小云粒子一直是多峰结构,峰值直径分别在3.5μm、12.5μm、23.5μm处.     

石家庄地区气溶胶和CCN垂直廓线的飞机观测分析

利用2010年春夏之交石家庄地区11架次的气溶胶和云凝结核(CCN)飞机同步观测资料,对比分析该地区云天和晴天气溶胶粒子的垂直廓线、不同高度气溶胶数谱特征,以及CCN的垂直分布、活化特性等。结果表明:云天气溶胶数浓度均值为1 553.28 cm~(-3),有效直径均值为0.52μm,比晴天数浓度(883.82 cm~(-3))大76%,有效直径(0.37μm)大41%。云天气溶胶数浓度呈指数型递减分布,有效半径在2 500 m以下随高度变化不明显,2 500 m以上随高度逐渐增大。晴天气溶胶数浓度在800～1 500 m内有累积,有效半径随高度没有明显的变化趋势。不同高度上气溶胶谱型基本一致,云天和晴天在气溶胶小尺度端(0.3μm)谱分布是连续的,在0.3μm处数谱均明显下降。云天和晴天CCN数浓度均随高度增大而减小,且各个高度层上云天CCN数浓度均大于晴天。云天CCN活化比率随高度变化不明显,晴天CCN活化比率随高度增大。气溶胶粒子尺度与CCN活化比率之间呈线性正相关。     

我国不同背景地区大气冰核浓度特征及参数化

为深入了解我国不同背景地区大气冰核浓度特征,本文通过在我国不同地区进行大气冰核及气溶胶的采样观测。研究发现：观测期间,黄山光明顶的冰核浓度数值均值为2.208 L^-1;南京地区的冰核浓度数值均值为7.16 L^-1;泰山山顶的冰核浓度数值均值为3.455 L^-1;泰山山底的冰核浓度数值均值为4.818 L^-1;新疆地区无沙尘天气冰核浓度数值均值为11.27 L^-1;新疆有沙尘天气冰核浓度数值均值为51.812 5 L^-1。研究给出了不同背景地区的大气冰核浓度的温度谱和湿度谱的分布。同时,研究发现,冰核数浓度与粒径大于0.5μm的气溶胶粒子数浓度的相关性较高,也就是气溶胶粒子中大颗粒所占比例越高,冰核数浓度越高。此外,还建立了基于活化温度、过饱和度以及大于0.5μm气溶胶粒子数浓度的冰核参数化方案,它们可以分别适用于沙漠地表,相对清洁的背景区域和人为污染较多的城市背景。     

衡水湖湿地气溶胶分布的飞机观测

利用机载粒子探测系统PMS（particle measurement system）对华北衡水湖湿地进行了一次晴空气溶胶飞机探测,研究结果表明：衡水湖上空气溶胶粒子比城市、城镇上空气溶胶粒子小。在低层,衡水湖上空气溶胶数密度比衡水市、枣强镇大;在高层,城市、城镇气溶胶数密度比衡水湖大许多。衡水湖地区气溶胶粒子直径绝大多数为0．1-0．25μm,直径为0．25—3．0μm的气溶胶粒子非常少。衡水湖上空与城市、城镇上空气溶胶特征和垂直分布不同。     

一次霾天气条件下石家庄上空大气气溶胶数浓度的飞行探测与特征分析

利用2010年8月30日河北省石家庄一次霾天气条件下的气溶胶飞行探测资料,分析了石家庄地区上空658—6933 m高度范围内大气气溶胶粒子平均数浓度、平均直径的垂直分布特征和9个水平飞行高度上的谱分布特征。结果表明:轻度霾天气条件下的气溶胶平均数浓度为325个/cm3,平均直径为0.169μm。在约1000 m高度以下,气溶胶平均数浓度随高度的增加呈线性减少趋势。粒径也随高度增加而减小,由0.187μm减小至0.164μm。1000 m高度以上,气溶胶平均数浓度随高度减少趋势变缓,粒子平均直径在0.167~0.171μm范围内波动。9个不同高度上的谱分布都呈单峰型,随着高度增加,谱宽变小,峰值向小尺度方向移动。后向轨迹计算分析表明:污染气团的远距离输送可能是导致大气1500 m高度层气溶胶数浓度突增的原因。     

Aerosol Type Identification Using PARASOL Multichannel Polarized Data

PARASOL （Polarization ＆ Anisotropy of Reflectances for Atmospheric Sciences coupled with Ob- servations from a Lidar） multi-channel and mul- ti-directional polarized data for different aerosol types were compared. The PARASOL polarized radiance data at 490 nm, 670 nm, and 865 nm increased with aerosol optical thickness （AOT） for fine-mode aerosols; however, the polarized radiances at 490 nm and 670 nm decreased as AOT increased for coarse dust aerosols. Thus, the vari- ation of the polarized radiance with AOT can be used to identify fine or coarse particle-dominated aerosols. Polar- ized radiances at three wavelengths for fine- and coarse-mode aerosols were analyzed and fitted by linear regression. The slope of the line for 670 nm and 490 nm wavelength pairs is less than 0.35 for dust aerosols. However, the value for fine-mode aerosols is greater than 0.60. The Support Vector Machine method （SVM） based on 12 vector features was used to discriminate clear sky, coarse dust aerosols, fine-mode aerosols, and cloud. Two cases were given and validated by AErosol RObotic NETwork （AERONET） measurements, MODIS （Mod- erate Resolution Imaging Spectroradiometer） FMF （Fine Mode Fraction at 550 nm） images, PARASOL RGB （Red Green Blue） images, and CALIOP （Cloud-Aerosol Lidar with Orthogonal Polarization） VFM （Vertical Feature Mask） data.     

Detecting Aerosols over Land from Satellites by Measuring Far IR Radiation from the Earth-Atmospheric System

In this study, a special method is proposed for detecting aerosols over land by analyzing satellite-measured far IR radiation at three channels, 8.7, 11.5, and 12.5 um. Sensitivity tests revealed that the behavioral features of radiative brightness temperatures (BTs) at these three channels with increasing optical depth are different among different types of aerosols. Analyzing how BTs and their differences, xBT (BT11.5-BT12.5) and yBT (BT8.7-BT11.5), behave with varying optical depth can help to qualitatively distinguish among aerosols and semi-quantitatively estimate their optical thicknesses. In addition, the authors found that the vertical density profile of aerosols has little impact on this method.     

大气对AVHRR通道反射太阳辐射各向异性的影响

在不同太阳天顶角及不同地表条件下，通过辐射传输计算，考察了大气对NOAA/AVHRR可见和近红外通道辐射强度各向异性转换系数的影响。结果表明，在地表为朗伯面的情况下，大气气溶胶有增强辐射强度的各向异性和改变辐射强度角分布型式的作用。     

不同污染条件下气溶胶对短波辐射通量影响的模拟研究

将高光谱分辨率的气溶胶光学参数化方案应用于高精度的辐射传输模式BCC_RAD（974带）中,研究不同污染状况下气溶胶在地表与近地层大气中造成的直接辐射强迫与辐射强迫效率。发现气溶胶在地表产生的直接辐射强迫为负,在近地层大气中产生的直接辐射强迫为正,且随气溶胶浓度的升高变大,说明大气气溶胶的含量越高,单位气溶胶光学厚度产生的直接辐射强迫越大。将短波划分为3个波段:紫外、可见光和近红外,发现在紫外、可见光和近红外波段中,不同污染状况下气溶胶在地表造成的直接辐射强迫范围分别为:-1.36—-13.66、-3.03—-32.41和-2.74—-28.62 W/m2,在近地层大气中产生的直接辐射强迫范围分别为0.44—4.26、0.99—9.80和0.93—8.87 W/m2。通过进一步对比自然和人为气溶胶的影响,发现人为气溶胶在地表和大气层顶产生的负直接辐射强迫以及对整层和近地面大气造成的正直接辐射强迫均大于自然气溶胶的影响,且上述两种排放源的气溶胶对整层大气辐射收支的影响主要集中在800 hPa高度以下的大气中。按照地表直接辐射强迫大小来分析不同种类气溶胶的影响,结果为硫酸盐>有机碳>黑碳>海盐>沙尘;按照近地层大气直接辐射强迫大小排序则为黑碳>有机碳>沙尘>海盐>硫酸盐。最后,通过分析散射型气溶胶与吸收型气溶胶对辐射通量的影响,还探究了大气中散射与吸收过程的异同。      

Effect of particle shape on dust shortwave direct radiative forcing calculations based on MODIS observations for a case study

Assuming spheroidal and spherical particle shapes for mineral dust aerosols, the effect of particle shape on dust aerosol optical depth retrievals, and subsequently on instantaneous shortwave direct radiative forcing (SWDRF) at the top of the atmosphere (TOA), is assessed based on Moderate Resolution Imaging Spectroradiometer (MODIS) data for a case study. Specifically, a simplified aerosol retrieval algorithm based on the principle of the Deep Blue aerosol retrieval method is employed to retrieve dust aerosol optical depths, and the Fu-Liou radiative transfer model is used to derive the instantaneous SWDRF of dust at the TOA for cloud-free conditions. Without considering the effect of particle shape on dust aerosol optical depth retrievals, the effect of particle shape on the scattering properties of dust aerosols (e.g., extinction efficiency, single scattering albedo and asymmetry factor) is negligible, which can lead to a relative difference of at most 5% for the SWDRF at the TOA. However, the effect of particle shape on the SWDRF cannot be neglected provided that the effect of particle shape on dust aerosol optical depth retrievals is also taken into account for SWDRF calculations. The corresponding results in an instantaneous case study show that the relative differences of the SWDRF at the TOA between spheroids and spheres depend critically on the scattering angles at which dust aerosol optical depths are retrieved, and can be up to 40% for low dust-loading conditions.     

1984～2000年印度洋与中国地区上空对流层中上层及平流层气溶胶变化和输送特征

利用美国SAGE II (Stratospheric Aerosol and Gas Experiment II)卫星最新版（6.0版）1.020 μm通道逐日气溶胶消光系数资料，得出了对流层中上层及平流层（10 km以上高度）气溶胶光学厚度的平均分布和变化特征。结果表明:气溶胶光学厚度在低纬度大，在印度洋的岛屿上空有三个高值中心，气溶胶光学厚度高值中心与对流层中上层的上升气流的高值中心相对应。与17年(1984～2000年)年平均相比，近6年（1995～2000年）孟加拉湾至青藏高原东南部上空气溶胶光学厚度明显增加；中国东部地区上空气溶胶光学厚度增加，中西部地区则减小。气溶胶光学厚度存在三个经向的增加带和两个经向的减小带。中纬度与赤道之间的布鲁尔-多普森环流（Brewer-Dobson Circulation）带来的低层大气与对流层中上层及平流层之间的气溶胶输送是导致气溶胶这种经向一致变化的主要因素。气溶胶的这种输送产生的近地面大气污染物向中上层大气输送有可能产生重要的气候变化。     

Identification of Aerosol Types and Their Optical Properties in the North China Plain Based on Long-Term AERONET Data

Characterization of aerosols is required to reduce uncertainties in satellite retrievals of global aerosols and for modeling the effects of these aerosols on climate.Aerosols in the North China Plain(NCP) are complex,which provides a good opportunity to study key aerosol optical properties for various aerosol types.A cluster analysis of key optical properties obtained from Aerosol Robotic Network(AERONET) data in Beijing and Xianghe during 2001-11 was performed to identify dominant aerosol types and their associated optical properties.Five dominant aerosol types were identified.The results show that the urban/industrial aerosol of moderate absorption was dominant in the region and that this type varied little with season.Urban/industrial aerosol of weak absorption was the next most common type and mainly occurs in summer,followed by that strong aerosols occurring mainly in winter.All were predominantly fine mode particles.Mineral dust(MD) and polluted dust(PD) occurred mainly in spring,followed by winter,and their absorption decreased with wavelength.In addition,aerosol dynamics and optical parameters such as refractive index and asymmetry factor were examined.Results show that the size of coarse mode particles decreased with AOD indicating the domination of external mixing between aerosols.     

Vertical distributions of aerosol optical properties during haze and floating dust weather in Shanghai

A comparative study on the vertical distributions of aerosol optical properties during haze and floating dust weather in Shanghai was conducted based on the data obtained from a micro pulse lidar.There was a distinct difference in layer thickness and extinction coefficient under the two types of weather conditions.Aerosols were concentrated below 1 km and the aerosol extinction coefficients ranged from 0.25 to 1.50km^-1 on haze days.In contrast,aerosols with smaller extinction coefficients(0.20 0.35 km^-1) accumulated mainly from the surface to 2 km on floating dust days.The seasonal variations of extinction and aerosol optical depth（AOD） for both haze and floating dust cases were similar greatest in winter,smaller in spring,and smallest in autumn.More than 85%of the aerosols appeared in the atmosphere below 1 km during severe haze and floating dust weather.The diurnal variation of the extinction coefficient of haze exhibited a bimodal shape with two peaks in the morning or at noon,and at nightfall,respectively.The aerosol extinction coefficient gradually increased throughout the day during floating dust weather.Case studies showed that haze aerosols were generated from the surface and then lifted up,but floating dust aerosols were transported vertically from higher altitude to the surface.The AOD during floating dust weather was higher than that during haze.The boundary layer was more stable during haze than during floating dust weather.     

兰州冬季气溶胶光学特性的参数化

兰州冬季气溶胶的谱分布用双谱模式拟合，即Junge谱加Deirmendjian谱；气溶胶的平均折射率为1.549-0.1i；气溶胶浓度随高度的分布根据天气条件取为高斯、均匀、指数分布三种类型。以此为基础，计算出兰州冬季气溶胶光学厚度的平均值。 经实测的气溶胶光学厚度与本文的计算值比较后发现，我们的参数化方案基本上是成功的。