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1.
华北部分地区云凝结核的观测分析 总被引：1，自引：0，他引：1
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。 相似文献
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南京不同天气和能见度下云凝结核的观测分析 总被引：3，自引：1，他引：2
利用美国DMT公司生产的云凝结核(Cloud Condensation Nuclei,CCN)计数器(DMTCCNC),对2013年4—12月南京地区CCN进行观测。对不同天气条件下CCN活化谱拟合,霾天C值最高,为13 085 cm-3,雨后C值降至8 054 cm-3,属于大陆性核谱。不同能见度条件下CCN活化谱特征有明显差异,南京地区不同程度霾天CCN数浓度均远高于轻雾天,浓雾时期CCN数浓度显著偏高。CCN数浓度受到气象要素和天气状况、气溶胶源排放等因素影响。南京地区气溶胶凝结核(Condensation Nuclei,CN)数浓度和CCN数浓度的拟合结果显示出较好的相关性。CCN数浓度值:冬季春季秋季夏季,春季CCN数浓度日变化有三峰趋势,夏季基本呈单峰型,秋季、冬季双峰特征突出。气溶胶源排放、环境气象条件和气溶胶理化特性均会影响CCN数浓度的季节变化。 相似文献
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《干旱气象》2016,(3)
2009年秋季利用夏延飞机观测平台对河北中南部雾霾天气条件下的气溶胶及云凝结核CCN进行观测,得到气溶胶、CCN数浓度及尺度的垂直廓线及粒子谱等特征,研究雾霾天大气气溶胶的分布、来源特征以及气溶胶与云凝结核的转化关系。研究发现:霾天气条件下边界层附近的气溶胶垂直分布特征有很大不同。边界层以上气溶胶浓度随高度递减,数浓度量级约101~102个·cm~(-3);边界层附近和近地面气溶胶浓度有峰值出现,近地面数浓度量级达103个·cm~(-3)。气溶胶粒子平均直径范围为0.16~0.18μm。600 m、1 000~2 000 m之间的气溶胶平均粒子谱大体呈单峰分布;3 000~4 000 m、6 000~6 900 m之间的粒子谱呈双峰分布。受气溶胶来源及特性差异的影响,在0.3%过饱和度下,3 000 m以下的气溶胶活化为CCN的比例不到20%,3 000 m以上活化比例高达50%。Hysplit后向轨迹模拟的气团移动轨迹显示,6 000 m以上的大气高层受我国西北地区远距离输送作用影响,沙尘粒子吸湿活化为CCN。低层气溶胶主要受下垫面及近地面污染排放影响,气溶胶尺度相对较小,气溶胶转化为CCN的比例低于高层。CCN浓度随过饱和度的增加呈增大趋势。利用多项式对气溶胶浓度和CCN浓度进行拟合,拟合结果与实测谱吻合较好。 相似文献
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黄山地区不同高度云凝结核的观测分析 总被引：2，自引：0，他引：2
为研究华东高山地区云凝结核（Cloud Condensation Nuclei,CCN）沿山峰的垂直变化特征,2011年6月利用云凝结核计数器（Cloud Condensation Nuclei Counter,CCNC）在黄山三个不同高度处对CCN进行观测。观测结果表明,不同高度的CCN浓度随时间的变化趋势基本一致,CCN浓度随高度的升高而减小,过饱和度为0.8%时山顶、山腰、山底CCN浓度平均值分别为1105.62、1218.39和1777.78 cm-3,山底的高CCN浓度（大于1000 cm-3）出现频率大于山腰和山顶,表明山底受周边污染源的影响较山顶和山腰大。山顶和山底的日变化曲线均为双峰型,两个峰值分别出现在午前和午后,与大气边界层高度及山谷风变化有关。利用公式N=CSk拟合了山顶在不同天气条件下CCN活化谱,并分析了其变化特征。结果显示,晴天、雨天和雾天的C值分别为2798、384、765,小于一些污染城市,属于清洁大陆型核谱。本文结果有助于改进对华东背景地区云凝结核时空分布的认识,为该地区云雾核化在数值模式中的表达提供观测依据和参数化方案。 相似文献
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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%。 相似文献
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为了对黄山地区云凝结核（Cloud Condensation Nuclei,CCN）进行闭合研究,2014年6月30日至7月28日在黄山光明顶对大气气溶胶理化性质和CCN数浓度进行观测,分析了气溶胶化学组分、谱分布以及CCN数浓度随时间变化的特征,通过κ-Köhler理论并使用离子配对法计算得到CCN数浓度与观测得到的CCN数浓度进行对比。结果表明：计算与观测的CCN闭合结果较好,低过饱和度CCN闭合结果好于高过饱和度,过饱和度较低时低估了CCN数浓度,而过饱和度较高时则高估了CCN数浓度,由此说明气溶胶的化学组分数据对预测CCN数浓度至关重要,同时说明该方法可以实现CCN的闭合。考虑到40%水溶性有机碳（Water Soluble Organic Carbon,WSOC）对气溶胶粒子吸湿性影响,在较低过饱和度CCN闭合结果较好,但影响效果并不显著,尤其是在拟合结果相对较差的高过饱和度下基本没有影响。因此,气溶胶粒子中水溶性无机组分对CCN活化有重要影响,而含量较多、化学组分复杂并且吸湿性不确定的WSOC对CCN活化影响较为有限,这与一些研究得出无机组分对于气溶胶吸湿性的影响比具有复杂特征的有机组分更重要的结论相符合。 相似文献
7.
晴空云凝结核垂直探测个例分析 总被引：2，自引：0，他引：2
利用机载DMT云凝结核计数器观测了2009年10月13日陕西关中西部晴空云凝结核（CCN）的垂直分布。分析结果显示：关中西部晴天地面CCN平均浓度在过饱和度为0.2%时大于10000个/cm3,大雾天气下地面CCN浓度明显高于晴天。CCN浓度随高度增加而递减,1500 m以下为高值区,1000 m、1550 m、4100 m、5500 m高度的CCN平均浓度在过饱和度为0.4%时分别为8827个/cm3、4439个/cm3、456个/cm3、504个/cm3。 相似文献
8.
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。 相似文献
9.
巨盐核对云滴活化影响的数值模拟研究 总被引：1，自引：1，他引：0
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. 相似文献
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D.M.CHATE R.T.WAGHMARE C.K.JENA V.GOPALAKRISHNAN P.MURUGAVEL Sachin D.GHUDE Rachana KULKARNI P.C.S.DEVARA 《大气科学进展》2018,35(2):218-223
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. 相似文献
12.
Gerson P. Almeida Stephan Borrmann João B. V. Leal Junior 《Meteorology and Atmospheric Physics》2014,125(3-4):159-176
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
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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 相似文献
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Surface measurements of cloud condensation nuclei (CCN) number concentration (cm−3) are presented for unmodified marine air and for polluted air at Mace Head, for the years 1994 and 1995. The CCN number concentration active at 0.5% supersaturation is found to be approximately log-normal for marine and polluted air at the site. Values of geometric mean, median and arithmetic mean of CCN number concentration (cm−3) for marine air are in the range 124–135, 140–150 and 130–157 for the two years of data. Analysis of CCN number concentration for high wind speed, U, up to 20 m s−1 show enhanced CCN production for U in excess of about 10–12 m s−1. Approximately 7% increase in CCN per 1 m s−1 increase in wind speed is found, up to 17 m s−1. A relationship of the form log10CCN=a+bU is obtained for the periods March 1994 and January, February 1995 for marine air yielding values a of 1.70; 1.90 and b of 0.035 for both periods. 相似文献
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Cloud condensation nuclei from biomass burning during the Amazonian dry-to-wet transition season 总被引：1，自引：0，他引：1
Jorge Alberto Martins Fábio Luiz T. Gonçalves Carlos A. Morales Gilberto F. Fisch Francisco Geraldo M. Pinheiro João Bosco V. Leal Júnior Carlos J. Oliveira Emerson M. Silva José Carlos P. Oliveira Alexandre A. Costa Maria Assunção F. Silva Dias 《Meteorology and Atmospheric Physics》2009,104(1-2):83-93
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. 相似文献
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感应电机矢量控制系统的仿真研究 总被引：6，自引：0，他引：6
根据2008年4—7月黄山大气气溶胶观测资料,研究了气溶胶粒子的数浓度、谱分布特征及其与气象因子的关系,探讨了雾天和非雾天气溶胶颗粒物时间和尺度分布特点。分析发现,黄山光明顶春、夏季大气气溶胶数浓度的平均值分别为3.14×103个/cm3和1.80×103个/cm3,其中超细粒子（粒径小于0.1μm的粒子）在春夏季分别约占总粒子数浓度的79%和68%;高数浓度值集中在粒径0.04～0.12μm;积聚模态气溶胶粒子（0.1～1.0μm）在体积浓度分布和表面积分布中占很大比例。结合气象资料比较了雾天与非雾天气溶胶分布的差异,发现细粒子浓度非雾天大于雾天,而气溶胶数浓度与温度呈正相关,与相对湿度成反相关。结果还发现,黄山在春季以西北风和偏南风为主,西北风时气溶胶数浓度较高,在夏季主要以偏南风,特别是西南风为主,但是气溶胶数浓度的高值多发生在偏东风的条件下。 相似文献