Vertical dynamic and thermodynamic characteristics of urban lower boundary layer and its relationship with aerosol concentration over Beijing   总被引：1，自引：0，他引：1  

ZHOU Mingyu  YAO Wenqing  XU Xiangde  YU Haiqing 《中国科学D辑(英文版)》2005,48(Z2)

By utilizing observational data from a 325 m tower of the Institute of Atmospheric Physics (IAP), Chinese Academy of Sciences (CAS) on March 19-29, 2001 and August 11-25, 2003, a comprehensive study was conducted on the vertical dynamical and thermodynamic characteristics of the urban lower boundary layer (ULBL) and its relationship with aerosol concentration over Beijing. Firstly, a comparative analysis was made on the gradient data (wind, temperature and humidity), ultrasonic data (atmospheric turbulences) and air-quality observations at different tower heights (47, 120 and 280 m). Secondly, a diagnosis was made to reveal the major features of normalized variances of velocity and temperature, turbulence kinetic energy as well as their relationship with aerosol concentrations. Furthermore, the characteristics of the ULBL vertical structure and the TSP concentration/distribution variations during a sand/dust weather process were also analyzed. The outcome of the study showed that under unstable stratification, the normalized variances of velocity (σu/u*, σv/u*, σw/u*) and temperature (σT/T*) at 47 and 120 m heights fit the Monin-Obukhov similarity (MOS) framework and the fitting formulas were given out accordingly. According to the stratification parameter (z′/L), the stable ULBL could be divided into 2 zones. With z′/L<0.1, it was a weakly stable zone and MOS framework was applicable. The other was a highly stable zone with z′/L>0.1 and the normalized velocity variances tended to increase along with higher stability, but it remained constant for normalized temperature variances. At daytime, the near-surface layer includes two heights of 47 and 120 m, while 280 m has been above it. The ULBL analysis in conjunction with a sand/dust weather process in Beijing in March 2001 indicated that the maximum concentration of Total Suspended Particulates (TSP) at 320 m reached 913.3 μg/m3 and the particles were transported from the upper to lower ULBL, which was apparently related to the development process of a low-level jet and its concomitant strong sinking motion.  相似文献   

Spatial character of the gaseous and particulate state compound correlation of urban atmospheric pollution in winter and summer   总被引：1，自引：0，他引：1  

XU Xiangde  SHI Xiaohui  XIE Lian  DING Guoan  MIAO Qiuju  MA Jianzhong  ZHENG Xiangdong 《中国科学D辑(英文版)》2005,48(Z2)

The spatial/temporal variation information of atmospheric dynamic-chemical processes at observation site points of the "canopy" boundary of Beijing urban building ensemble and over urban area "surface", as well as the seasonal correlation structure of the gaseous and particulate states of urban atmospheric pollution (UAP) and its seasonal conversion feature at observation points are investigated, using the comprehensive observation data of the Beijing City Air Pollution Observation Experiment (BECAPEX) in winter and summer 2003 with a "point-surface" combined research approach. By using "one dimension spatial empirical orthogonal function (EOF)" principal component analysis (PCA) mode, the seasonal change of gaseous and particulate states of atmospheric aerosols and the association feature of pollutant species under the background of the complicated structure of urban boundary layer (UBL) are analyzed. The comprehensive analyses of the principal components of particle concentrations,gaseous pollutant species, and meteorological conditions reveal the seasonal changes of the complex constituent and structure features of the gaseous and particulate states of UAP to further trace the impact feature of urban aerosol pollution surface sources and the seasonal difference of the component structure of UAP. Research results suggest that in the temporal evolution of the gaseous and particulate states of winter/summer UAP, NOx, CO, and SO2 showed an "in-phase" evolution feature, however, O3 showed an "inverse-phase" relation with other species,all possessing distinctive dependent feature. On the whole, summer concentrations of gaseous pollutants CO, SO2, and NOx were obviously lower than winter ones, especially, the reduction in CO concentration was most distinctive, and ones in SO2 and NOx were next. However, the summer O3 concentration was more than twice winter one. Winter/summer differences in PM10and PM2.5 particle concentrations were relatively not obvious, which indicates that responses of PM10 and PM2.5 particle concentrations to the difference of winter/summer heating period emission sources are far less distinctive than those of NOx, SO2, and CO. The correlation feature of winter/summer gaseous and particulate states depicts that both PM10 and PM2.5 particles were significantly correlated with NOx, and their correlations with NOx are more significant than those with other pollutants. Through PCA, it is found that there was a distinctive difference in the principal component combination structure of winter/summer PM10 and PM2.5 particles: SO2 and NOx dominated in the principal component of winter PM10 and PM2.5 particles; while CO and NOx played the major role in the principal component of summer PM10 and PM2.5 particles. For winter/summer PM10 and PM2.5 particles, there might exist the gaseous and particulate states correlation structures of different "combinations" of such dependent pollutant species. Research results also uncover that the interaction processes of gaseous and particulate states were also related with the vertical structure of UBL, that is to say, the low value layer of UBL O3 concentration was associated with the collocation of atmospheric vertical structures of the low level inversion,inverse humidity, and small wind, which depicts summer boundary layer atmospheric character, i.e.the compound impact of the dependent factor "combination" of wind, temperature, and humidity elements and their collocation structure on the variations of different gaseous pollutant concentrations. Such a depth structure of the extremely low value of O3 concentration in the UBL accords with its "inverse-phase" relation with other gaseous pollutant species. The PCA of meteorological factors associated with PM10 and PM2.5 concentrations also reveals the sensitivity of PM10 and PM2.5 concentration to the combinatory feature of local meteorological conditions.  相似文献   

基于FY3A/MERSI资料分析广东省气溶胶光学厚度分布   总被引：3，自引：3，他引：0  

邓玉娇  胡猛  林楚勇  曹静 《气象》2016,42(1):61-66

利用国产极轨气象卫星FY3A的MERSI AOD产品分析2010—2013年广东省气溶胶光学厚度的分布规律。结果表明:MERSI AOD产品与地面太阳光度计实测数据的相关系数为0.72,其平均绝对值误差为0.12,均方根误差为0.15,数据精度可满足研究需要;从AOD的空间分布看,珠三角西翼东翼山区五市,其中佛山市、东莞市、中山市为广东省AOD均值最高的地区,梅州市、河源市为广东省AOD均值最低的地区;从AOD的时间分布看,2010—2013年间,AOD呈现先升高后降低的趋势,2011年为拐点,与此同时,AOD还表现出明显的季节变化特征,春季为AOD高值期,夏季、秋季次之,冬季最低。  相似文献   

天津城区春节期间大气气溶胶污染特征 和数浓度分布     

姚青  刘敬乐  韩素芹  樊文雁 《气象》2016,42(4):443-449

利用天津城区2009-2014年春节期间大气气溶胶观测资料和相关气象资料,重点分析2013和2014年春节期间气溶胶污染特征,探求燃放烟花爆竹以及气象条件对春节期间大气气溶胶的影响。结果表明,受燃放烟花爆竹影响,春节期间PM_(2.5)质量浓度最高值均发生在除夕夜间;持续雾霾天气条件下燃放烟花爆竹,造成2013年除夕夜间PM_(2.5)质量浓度峰值达到1240μg·m～(-3),是近年来最严重的一次;2014年春节期间烟花爆竹燃放量有所减少,加之空气扩散条件较为有利,PM_(2.5)质量浓度显著低于2013年;不同天气条件下,气溶胶数浓度谱分布特征存在明显差异,燃放烟花爆竹期间气溶胶数浓度水平与严重雾-霾天气相当。  相似文献   

太湖地区HJ-1卫星CCD数据反演气溶胶及大气校正     

郑尧  王琪洁  梁忠壮 《测绘工程》2016,25(5):10-15

针对HJ-1卫星CCD数据,利用改进的暗像元法反演气溶胶光学厚度(AOD),再利用反演的AOD对其进行大气校正。将反演的气溶胶与地基太阳光度计数据进行对比验证,发现当反演的AOD值大于0.2时,反演值与地基观测值的相关系数为0.964,符合MODIS业务化反演AOD的精度要求。再将反演得到的气溶胶带入6S辐射传输模型中,对HJ-1卫星CCD数据进行大气校正实验。结果表明,该方法能有效提高HJ-1卫星CCD数据大气校正的精度,更好地复原地物的真实光谱信息。  相似文献   

气溶胶大气辐射校正区域性分析     

刘小力  王琪洁  张勇  梁忠壮 《测绘科学》2016,41(4):55-60,82

针对使用6S模型中标准气溶胶模型进行大气辐射校正时结果较差的问题,该文提出使用实测气溶胶模型代替其进行计算。利用AERONET数据产品分析了香河、榆中等部分站点的气溶胶成分及其区域性分布特点,证明了中国气溶胶的成分具有明显的区域特性;并对6S模型中标准气溶胶模型与香河地基观测气溶胶光学参数进行比较,结果表明,两者具有较大的差异;最后使用不同的气溶胶模型校正Landsat5TM影像,结果表明,采用实测气溶胶数据进行大气辐射校正结果较优。  相似文献   

Satellite-measured atmospheric aerosol content in Korea: anthropogenic signals from decadal records     

Sunyurp Park 《地理信息系统科学与遥感》2016,53(5):634-650

Spatiotemporal characteristics and anthropogenic signals of aerosol optical thickness (AOT) distributions over Korea are investigated in this study using AOT time-series data from the Moderate Resolution Imaging Spectroradiometer (MODIS). AOT observations, a quantitative measure of the atmospheric quality, had significant geographical variations during the study period (2000–2010). Comparing metro cities or counties with similar populations, western regions showed higher AOT values than eastern regions. Particular matter with a diameter < 10 µm (PM₁₀), including aeolian dust or yellow dust, is the primary component of atmospheric aerosols, and their transport into the region has shown a strong seasonal pattern with its peak from March to April and lows from July to September. These seasonal dust patterns, however, did not correspond well to temporal AOT records, which typically reached the maximum level in June nationwide. Rather, widespread regional fire events and humidity showed significant correlations with AOT time-series. This correlation rapidly increased as the range of fire occurrence was extended to the west as far as 115°E. The relative humidity also had a significant correlation with AOT during the month of June. In addition to urban emission of anthropogenic aerosols, regional biomass burning and secondary growth of hygroscopic aerosols are considered important contributors to the degradation of the atmospheric environment during the non-Asian Dust season over the Korean Peninsula.  相似文献   

利用分布式光纤声传感设备开展青藏高原易贡湖浅层结构探测     

张衡  徐团伟  裴顺平  赵俊猛 《地学前缘》2021,28(6):227-234

地震数据是利用地震学方法探测地下结构的基础条件,然而传统地震仪器难以获得极端环境地区(水下、高原等)的长时间、高密度连续数据。较之国际仪器厂商,国内的DAS研制相对较晚。自2016年起,国产DAS逐步应用于石油测井和城市区域地下结构探测,而运用在极端环境下的探测工作尚未见报道。中国科学院半导体研究所与青藏高原研究所经过多年合作研究,于2021年4月将自主研发的DAS系统首次应用于青藏高原的野外数据采集。本次试验同时记录了地面和水下的连续背景噪声和重锤数据。该研究利用背景噪声成像技术,获得了西藏易贡湖地区地表70 m以内的横波速度结构。本次研究为极端环境下的低成本、高密度数据采集和地下结构探测提供了理论和试验依据。  相似文献   

Simulation and Validation of the Aerosol Optical Thicknessover China in 2006     

ZHANG Hu  ZHANG Min  CUI Zhenlei  WANG Yuesi  XIN Jinyuan 《Acta Meteorologica Sinica》2012,26(3):330-344

  相似文献   

Nitrogen and sulfur species in Antarctic aerosols at Mawson,Palmer Station,and Marsh (King George Island)   总被引：4，自引：0，他引：4  

D. L. Savoie  J. M. Prospero  R. J. Larsen  F. Huang  M. A. Izaguirre  T. Huang  T. H. Snowdon  L. Custals  C. G. Sanderson 《Journal of Atmospheric Chemistry》1993,17(2):95-122

High volume bulk aerosol samples were collected continuously at three Antarctic sites: Mawson (67.60° S, 62.50° E) from 20 February 1987 to 6 January 1992; Palmer Station (64.77° S, 64.06° W) from 3 April 1990 to 15 June 1991; and Marsh (62.18° S, 58.30° W) from 28 March 1990, to 1 May 1991. All samples were analyzed for Na⁺, SO ₄ ^2– , NO ₃ ^– , methanesulfonate (MSA), NH ₄ ⁺ ,²¹⁰Pb, and⁷Be. At Mawson for which we have a multiple year data set, the annual mean concentration of each species sometimes vary significantly from one year to the next: Na⁺, 68–151 ng m^–3; NO ₃ ^– , 25–30 ng m^–3; nss SO ₄ ^2– , 81–97 ng m^–3; MSA, 19–28 ng m^–3; NH ₄ ⁺ , 16–21 ng m^–3;²¹⁰Pb, 0.75–0.86 fCi m^–3. Results from multiple variable regression of non-sea-salt (nss) SO ₄ ^2– with MSA and NO ₃ ^– as the independent variables indicates that, at Mawson, the nss SO ₄ ^2– /MSA ratio resulting from the oxidation of dimethylsulfide (DMS) is 2.80±0.13, about 13% lower than our earlier estimate (3.22) that was based on 2.5 years of data. A similar analysis indicates that the ratio at Palmer is about 40% lower, 1.71±0.10, and more comparable to previous results over the southern oceans. These results when combined with previously published data suggest that the differences in the ratio may reflect a more rapid loss of MSA relative to nss SO ₄ ^2– during transport over Antarctica from the oceanic source region. The mean²¹⁰Pb concentrations at Palmer and Marsh and the mean NO ₃ ^– concentration at Palmer are about a factor of two lower than those at Mawson. The²¹⁰Pb distributions are consistent with a²¹⁰Pb minimum in the marine boundary layer in the region of 40°–60° S. These features and the similar seasonalities of NO ₃ ^– and²¹⁰Pb at Mawson support the conclusion that the primary source regions for NO ₃ ^– are continental. In contrast, the mean concentrations of MSA, nss SO ₄ ^2– , and NH ₄ ⁺ at Palmer are all higher than those at Mawson: MSA by a factor of 2; nss SO ₄ ^2– by 10%; and NH ₄ ⁺ by more than 50%. However, the factor differences exhibit substantial seasonal variability; the largest differences generally occur during the austral summer when the concentrations of most of the species are highest. NH ₄ ⁺ /(nss SO ₄ ^2– +MSA) equivalent ratios indicate that NH₃ neutralizes about 60% of the sulfur acids during December at both Mawson and Palmer, but only about 30% at Mawson during February and March.  相似文献