Impacts of Aerosol-Radiation Interactions on the Wintertime Particulate Pollution under Different Synoptic Patterns in the Guanzhong Basin,China

The effects of aerosol–radiation interactions(ARI) are not only important for regional and global climate, but they can also drive particulate matter(PM) pollution. In this study, the ARI contribution to the near-surface fine PM(PM2.5)concentrations in the Guanzhong Basin(GZB) is evaluated under four unfavorable synoptic patterns, including "northlow", "transition", "southeast-trough", and "inland-high", based on WRF-Chem model simulations of a persistent heavy PM pollution episode in January 2019. Simulations show that ARI consistently decreases both solar radiation reaching down to the surface(SWDOWN) and surface temperature(TSFC), which then reduces wind speed, induces sinking motion,and influences cloud formation in the GZB. However, large differences under the four synoptic patterns still exist. The average reductions of SWDOWN and daytime TSFC in the GZB range from 15.2% and 1.04°C in the case of the"transition" pattern to 26.7% and 1.69°C in the case of the "north-low" pattern, respectively. Furthermore, ARI suppresses the development of the planetary boundary layer(PBL), with the decrease of PBL height(PBLH) varying from 18.7% in the case of the "transition" pattern to 32.0% in the case of the "north-low" pattern. The increase of daytime near-surface PM2.5 in the GZB due to ARI is 12.0%, 8.1%, 9.5%, and 9.7% under the four synoptic patterns, respectively. Ensemble analyses also reveal that when near-surface PM2.5 concentrations are low, ARI tends to lower PM2.5 concentrations with decreased PBLH, which is caused by enhanced divergence or a transition from divergence to convergence in an area. ARI contributes 15%–25% toward the near-surface PM2.5 concentrations during the severe PM pollution period under the four synoptic patterns.     

Ground-Based In Situ Measurements of Near-Surface Aerosol Mass Concentration over Anantapur: Heterogeneity in Source Impacts

Surface measurements of aerosol physical properties were made at Anantapur(14.62°N,77.65 °E,331 m a.s.l),a semiarid rural site in India,during August 2008-July 2009.Measurements included the segregated sizes of aerosolsas as well as total mass concentration and size distributions of aerosols measured at low relative humidity(RH<75%) using a Quartz Crystal Microbalance(QCM) in the 25-0.05 μm aerodynamic diameter range.The hourly average total surface aerosol mass concentration in a day varied from 15 to 70 μg m-3,with a mean value of 34.02±9.05μgm-3 for the entire study period.A clear diurnal pattern appeared in coarse,accumulation and nucleation-mode particle concentrations,with two local maxima occurring in early morning and late evening hours.The concentration of coarse-mode particles was high during the summer season,with a maximum concentration of 11.81±0.98μgm-3 in the month of April,whereas accumulationmode concentration was observed to be high in the winter period contributed >68% to the total aerosol mass concentration.Accumulation aerosol mass fraction,A f(=Ma/Mt) was highest during winter(mean value of Af～0.80) and lowest(Af～0.64) during the monsoon season.The regression analysis shows that both R eff and R m are dependent on coarse-mode aerosols.The relationship between the simultaneous measurements of daily mean aerosol optical depth at 500 nm(AOD500) and PM 2.5 mass concentration([PM2.5]) shows that surface-level aerosol mass concentration increases with the increase in columnar aerosol optical depth over the observation period.     

VARIATION CHARACTERISTICS OF THE PLANETARY BOUNDARY LAYER HEIGHT AND ITS RELATIONSHIP WITH PM2.5 CONCENTRATION OVER CHINA

The planetary boundary layer height (PBLH) was calculated using the radiosonde sounding data, including 120 L-band operational sites and 8 GPS sites in China. The diurnal and seasonal variations of PBLH were analyzed using radiosonde sounding (OBS-PBLH) and ERA data (ERA-PBLH). Based on comparison and error analyses, we discussed the main error sources in these data. The frequency distributions of PBLH variations under different regimes (the convective boundary layer, the neutral residual layer, and the stable boundary layer) can be well fitted by a Gamma distribution and the shape parameter k and scale parameter s values were obtained for different regions of China. The variation characteristics of PBLH were found in summer under these three regimes for different regions. The relationships between PBLH and PM2.5 concentration generally follow a power law under very low or no precipitation conditions in the region of Beijing, Tianjin and Hebei in summer. The results usually deviated from this power distribution only under strong precipitation or high relative humidity conditions because of the effects of hygroscopic growth of aerosols or wet deposition. The OBS-PBLH provided a reasonable spatial distribution relative to ERA-PBLH. This indicates that OBS-PBLH has the potential for identifying the variation of PM2.5 concentration.     

基于激光云高仪反演全天边界层高度的两步曲线拟合法

大气边界层高度是天气、气候、大气环境研究中的一个重要参数,目前尚缺少基于激光雷达探测系统反演全天边界层高度的有效方法。文中利用北京朝阳站、大兴站的激光云高仪数据,首先评估了梯度法、标准偏差法、曲线拟合法和小波协方差法反演边界层高度的适用性和局限性,发现梯度法容易受环境噪声的影响,曲线拟合法稳定性较好,但在夜间弱湍流条件下会将残留层高度误判为夜间边界层高度。提出两步曲线拟合法,将一天中边界层结构划分为白天的对流边界层、夜间的残留层和稳定边界层,通过用不同的理想曲线对其进行两步拟合,获取全天边界层高度的变化。将两步曲线拟合法的反演结果与基于L波段探空雷达的位温梯度法的探测结果进行比较发现:两者相关系数为0.91,证明了两步曲线拟合法的可行性以及激光云高仪探测边界层高度的应用潜力。采用该方法反演2017年5—6月朝阳站与大兴站边界层高度,对比发现:城区特殊的下垫面性质使朝阳站日间对流边界层发展更早,边界层高度更高,全天朝阳站边界层高度的变化在308—1391 m,大兴站在197—1302 m。      

天津夏季大气消光性质的研究

利用2010年夏季天津城市边界层观测站颗粒物、黑碳气溶胶、氮氧化物(NOX)浓度、地面能见度和气象梯度观测资料,分析了天津夏季大气消光特性及低能见度事件产生的原因。结果表明,天津夏季主要污染物为PM10和PM2.5,大气气溶胶消光系数为529.06M.m-1,其中,吸收系数为50.17M.m-1,散射系数为478.89M.m-1,气体吸收系数为7.74M.m-1,气溶胶单次散射反射率为0.87。天津夏季边界层大气状态有近一半的时间为中性或偏稳定层结,当出现中性或偏稳定层结大气时则有接近一半的情况出现低能见度事件(能见度<5km),影响人们的日常生活。     

Retrieval of Boundary Layer Height and Its Influence on PM 2.5 Concentration Based on Lidar Observation over Guangzhou

Wavelet analysis was applied to lidar observations to retrieve the planetary boundary layer height(PBLH)over Guangzhou from September 2013 to November 2014 over Guangzhou. Impact of the boundary effect and the wavelet scale factor on the accuracy of the retrieved PBLH has been explored thoroughly. In addition, the PBLH diurnal variations and the relationship between PM_(2.5) concentration and PBLH during polluted and clean episodes were studied. Results indicate that the most steady retrieved PBLH can be obtained when scale factor is chosen between 300-390 m. The retrieved maximum and minimum PBLH in the annual mean diurnal cycle were ～1100 m and ～650 m, respectively. The PBLH was significantly lower in the dry season than in the wet season, with the average highest PBLH in the dry season and the wet season being ～1050 m and ～1200 m respectively. Compared to the wet season, the development of PBLH in the dry season was delayed by at least one hour due to the seasonal cycle of solar radiation. Episode analysis indicated that the PBLH was ～50% higher during clean episodes than during haze episodes. The average highest PBLH in the haze episodes and clean episodes were ～800 m and ～1300 m,respectively. A significant negative correlation between PBLH and PM_(2.5) concentration(r =-0.55**) is discovered.According to China"Ambient Air Quality Standard", the PBLH values in good and slightly polluted conditions were 1/6-1/3 lower than that in excellent conditions, while the corresponding PM_(2.5) concentration were ～2-2.5 times higher.     

Comparison of Two Air Pollution Episodes over Northeast China in Winter 2016/17 Using Ground-Based Lidar

This study analyzes and compares aerosol properties and meteorological conditions during two air pollution episodes in 19–22 (E1) and 25–26 (E2) December 2016 in Northeast China. The visibility, particulate matter (PM) mass concentration, and surface meteorological observations were examined, together with the planetary boundary layer (PBL) properties and vertical profiles of aerosol extinction coefficient and volume depolarization ratio that were measured by a ground-based lidar in Shenyang of Liaoning Province, China during December 2016–January 2017. Results suggest that the low PBL height led to poor pollution dilution in E1, while the high PBL accompanied by low visibility in E2 might have been due to cross-regional and vertical air transmission. The PM mass concentration decreased as the PBL height increased in E1 while these two variables were positively correlated in E2. The enhanced winds in E2 diffused the pollutants and contributed largely to the aerosol transport. Strong temperature inversion in E1 resulted in increased PM_2.5 and PM₁₀ concentrations, and the winds in E2 favoured the southwesterly transport of aerosols from the North China Plain into the region surrounding Shenyang. The large extinction coefficient was partially attributed to the local pollution under the low PBL with high ground-surface PM mass concentrations in E1, whereas the cross-regional transport of aerosols within a high PBL and the low PM mass concentration near the ground in E2 were associated with severe aerosol extinction at high altitudes. These results may facilitate better understanding of the vertical distribution of aerosol properties during winter pollution events in Northeast China.     

秸秆燃烧对北京秋季气溶胶浓度和短波辐射影响的模拟研究

利用地面细颗粒物（PM2.5）浓度和气象常规观测资料、地基 AERONET观测资料、GFED生物质燃烧排放清单和大气化学—天气耦合模式WRF-Chem,模拟研究了华北地区2014年10月气象要素和大气污染物的时空演变,重点关注北京10月7～11日的一次重霾事件及其天气形势、边界层气象特征、输送路径、PM2.5及其化学成分浓度变化等特征,以及秸秆燃烧对华北和北京地区细颗粒物浓度和地面短波辐射的影响。与观测资料的对比结果显示,模式可以很好地模拟北京地区地面气象要素和PM2.5质量浓度,考虑秸秆燃烧排放源可以明显改进北京PM2.5浓度模拟的准确性,但在重度污染情况下,模式总体上低估气溶胶光学厚度和高估地面短波辐射。10月7～11日北京地区重霾事件主要是不利气象条件下人为污染物累积和区域输送造成,也受到华北地区南部秸秆燃烧的影响。河南北部、河北南部和山东西部大面积秸秆燃烧释放的气态污染物和颗粒物在南风的作用下输送至北京,秸秆燃烧对北京地区地面PM2.5、有机碳（OC）、硝酸盐、铵盐、硫酸盐和黑碳（BC）的平均贡献率分别为24.6%、36.8%、23.2%、22.6%、7.1%和19.8%,秸秆燃烧产生的气溶胶可以导致北京地面平均短波辐射最大减小超过20 W m－2,约占总气溶胶导致地表短波辐射变化的24%。     

京津冀一次重度雾霾天气能见度及边界层关键气象要素的模拟研究

本文利用GRAPES_CUACE大气化学模式对京津冀地区2015年12月重度雾霾过程进行了模拟和评估。京津冀地区能见度和PM_2.5模拟值与观测值的对比表明:该模式能较好地模拟京津冀地区能见度和PM_2.5的逐日变化情况,但模式存在对伴随着重污染发生的低能见度模拟偏高的问题。以12月5~10日的重度雾霾过程为重点,针对地面风速、边界层高度、相对湿度、PM_2.5及其对能见度的影响进行了详细分析,研究结果表明:污染过程中大部分地区过程平均风速低于2 m s-1,边界层平均高度低于600 m,相对湿度较高。模式低能见度模拟偏高可能因为:（1）模式模拟重雾霾时段的PM_2.5极大值浓度偏低。（2）模拟相对湿度存在系统性偏低的误差,这一误差对能见度的影响表现为两方面,一是相对湿度会通过影响可溶性气溶胶的吸湿增长过程影响气溶胶质量浓度,导致气溶胶消光系数的计算偏低;二是目前模式中采用的能见度的参数化公式考虑了相对湿度对气溶胶吸湿增长的影响,没有考虑雾滴的直接消光作用。     

Characterization of Organic Aerosol at a Rural Site in the North China Plain Region: Sources,Volatility and Organonitrates

The North China Plain(NCP) is a region that experiences serious aerosol pollution. A number of studies have focused on aerosol pollution in urban areas in the NCP region; however, research on characterizing aerosols in rural NCP areas is comparatively limited. In this study, we deployed a TD-HR-AMS(thermodenuder high-resolution aerosol mass spectrometer) system at a rural site in the NCP region in summer 2013 to characterize the chemical compositions and volatility of submicron aerosols(PM_1). The average PM_1 mass concentration was 51.2 ± 48.0 μg m~(-3) and organic aerosol(OA) contributed most(35.4%) to PM_1. Positive matrix factorization(PMF) analysis of OA measurements identified four OA factors, including hydrocarbon-like OA(HOA, accounting for 18.4%), biomass burning OA(BBOA, 29.4%), lessoxidized oxygenated OA(LO-OOA, 30.8%) and more-oxidized oxygenated OA(MO-OOA, 21.4%). The volatility sequence of the OA factors was HOA BBOA LO-OOA MO-OOA, consistent with their oxygen-to-carbon(O:C)ratios. Additionally, the mean concentration of organonitrates(ON) was 1.48-3.39 μg m~(-3), contributing 8.1%–19% of OA based on cross validation of two estimation methods with the high-resolution time-of-flight aerosol mass spectrometer(HRToF-AMS) measurement. Correlation analysis shows that ON were more correlated with BBOA and black carbon emitted from biomass burning but poorly correlated with LO-OOA. Also, volatility analysis for ON further confirmed that particulate ON formation might be closely associated with primary emissions in rural NCP areas.     

Simulationsof Aerosol Optical Properties to Top of Atmospheric Reflected Sunlight in the Near Infrared CO2 Weak Absorption Band

Over the Asian continent,high aerosol loading is critical to ensure the high accuracy of CO₂ retrieval in the near infrared absorption band.Simulations were performed to explore the effect of light path modification by aerosol son the atmospheric CO₂ near infrared band(6140-6270 cm^-1).The Vector LInearized Discrete Ordinate Radiative Transfer（VLIDORT） model and the Line-By-Line Radiative Transfer Model（LBLRTM） were used for forward calculations.The U.S.standard atmosphere was used for atmospheric profiles.The results indicate that the aerosols caused similar effects to increases in CO₂ in the planetary boundary layer and became more significant with aerosol layer rising while aerosol optical depth was 0.1.This effect will cause an over estimation of the CO₂ mixing ratio in the retrieval process and an under estimation in the aerosol layer.The results also indicate that the effect of urban and industrial aerosols is smaller than that of non-absorbing and dust aerosols because of the nearly constant absorption properties in the near infrared band.     

中国东部气溶胶在天气尺度上的辐射强迫和对地面气温的影响

本文应用WRF-Chem(Weather Research and Forecasting—Chemistry)模式研究中国东部地区气溶胶及其部分组分(硫酸盐、硝酸盐和黑碳气溶胶)在天气尺度下的辐射强迫和对地面气温的影响。5个无明显降水时间段(2006年8月23～25日、2008年11月10～12日、2008年12月16～18日、2009年1月15～17日和2009年4月27～29日)的模拟显示,气溶胶浓度呈现显著的白天低,夜间高的日变化特征,且北方区域(29.8°～42.6°N,110.2°～120.3°E)平均PM_2.5近地面浓度(40～80 μg m-3)高于南方区域(22.3°～29.9°N,109.7°～120.2°E,30～47 μg m-3)。气溶胶对地面2 m温度(地面气温)有明显的降温效果,在早上08:00(北京时,下同)和下午17:00左右最为显著,最高可降低约0.2～1 K,同时气溶胶的参与改善了模式对地面气温的模拟。本文还通过对2006年8月23～25日一次个例的模拟,定量分析了气溶胶及其部分组分(硫酸盐、硝酸盐和黑碳气溶胶)的总天气效应(直接效应+间接效应)、直接效应和间接效应分别对到达地面的短波辐射和地面气温的影响。北方区域平均气溶胶直接效应所造成的短波辐射强迫要高于南方区域,分别为-11.3 W m-2和-5.8 W m-2,导致地面气温分别降低了0.074 K和0.039 K。南方区域平均气溶胶间接效应所产的短波辐射强迫高于北方区域,分别为-14.4 W m-2和-12.4 W m-2,引起的地面气温的改变分别为-0.094 K和-0.035 K。对于气溶胶组分,硫酸盐气溶胶的直接效应和间接效应的作用相当,其总效应在北方和南方区域平均短波辐射强迫分别为-7.0 W m-2和-10.5 W m-2,对地面气温的影响为-0.062 K和-0.074 K,而硝酸盐气溶胶的作用略小。黑碳气溶胶使得北方和南方区域平均到达地表的太阳短波辐射分别减少了6.5 W m-2和5.8 W m-2,而地表气温则分别增加了0.053 K和0.017 K,相比于间接效应,黑碳气溶胶的直接效应的影响更加显著。     

Evolution of aerosol vertical distribution during particulate pollution events in Shanghai

A set of micro pulse lidar(MPL)systems operating at 532 nm was used for ground-based observation of aerosols in Shanghai in 2011.Three typical particulate pollution events(e.g.,haze)were examined to determine the evolution of aerosol vertical distribution and the planetary boundary layer(PBL)during these pollution episodes.The aerosol vertical extinction coefficient(VEC)at any given measured altitude was prominently larger during haze periods than that before or after the associated event.Aerosols originating from various source regions exerted forcing to some extent on aerosol loading and vertical layering,leading to different aerosol vertical distribution structures.Aerosol VECs were always maximized near the surface owing to the potential influence of local pollutant emissions.Several peaks in aerosol VECs were found at altitudes above 1 km during the dust-and bioburning-influenced haze events.Aerosol VECs decreased with increasing altitude during the local-polluted haze event,with a single maximum in the surface atmosphere.PM2.5 increased slowly while PBL and visibility decreased gradually in the early stages of haze events;subsequently,PM2.5 accumulated and was exacerbated until serious pollution bursts occurred in the middle and later stages.The results reveal that aerosols from different sources impact aerosol vertical distributions in the atmosphere and that the relationship between PBL and pollutant loadings may play an important role in the formation of pollution.     

Modeling Study of the Impact of Heterogeneous Reactions on Dust Surfaces on Aerosol Optical Depth and Direct Radiative Forcing over East Asia in Springtime

The spatial distributions and interannual variations of aerosol concentrations,aerosol optical depth(AOD) ,aerosol direct radiative forcings,and their responses to heterogeneous reactions on dust surfaces over East Asia in March 2006-10 were investigated by utilizing a regional coupled climate-chemistry/aerosol model. Anthropogenic aerosol concentrations(inorganic+carbonaceous) were higher in March 2006 and 2008,whereas soil dust reached its highest levels in March 2006 and 2010,resulting in stronger aerosol radiative forcings in these periods.The domain and five-year(2006-10) monthly mean concentrations of anthropogenic and dust aerosols,AOD,and radiative forcings at the surface(SURF) and at the top of the atmosphere(TOA) in March were 2.4μg m-3,13.1μg m-3,0.18,-19.0 W m-2,and-7.4 W m-2,respectively.Heterogeneous reactions led to an increase of total inorganic aerosol concentration;however,the ambient inorganic aerosol concentration decreased,resulting in a smaller AOD and weaker aerosol radiative forcings.In March 2006 and 2010,the changes in ambient inorganic aerosols,AOD,and aerosol radiative forcings were more evident.In terms of the domain and five-year averages,the total inorganic aerosol concentrations increased by 13.7%(0.17μg m-3) due to heterogeneous reactions,but the ambient inorganic aerosol concentrations were reduced by 10.5%(0.13μg m-3) .As a result,the changes in AOD,SURF and TOA radiative forcings were estimated to be-3.9%(-0.007) ,-1.7%(0.34 W m-2) ,and-4.3%(0.34 W m-2) ,respectively,in March over East Asia.     

Chemical Composition of Summertime PM2.5 and Its Relationship to Aerosol Optical Properties in Guangzhou, China

Urban aerosols have a large effect on the deterioration of air quality and the degradation of atmospheric visibility.Characterization of the chemical composition of PM 2.5 and in situ measurements of the optical properties of aerosols were conducted in July 2008 at an urban site in Guangzhou,Southern China.The mean PM 2.5 concentration for the entire period was 53.7±23.2 μg m 3.The mean PM 2.5 concentration (82.7±25.4 μg m 3) on hazy days was roughly two times higher than that on clear days (38.8±8.7 μg m 3).The total water-soluble ion species and the total average carbon accounted for 47.9%±4.3% and 35.2%±4.5%,respectively,of the major components of PM 2.5.The increase of secondary and carbonaceous aerosols,in particular ammonium sulfate,played an important role in the formation of haze pollution.The mean absorption and scattering coefficients and the single scattering albedo over the whole period were 53±20 M m 1,226±111 M m 1,and 0.80±0.04,respectively.PM 2.5 had a high linear correlation with the aerosol extinction coefficient,elemental carbon (EC) was correlated with aerosol absorption,and organic carbon (OC) and SO 4 2 were tightly linked to aerosol scattering.     

Effects of arctic sulphuric acid aerosols on wintertime low-level atmospheric ice crystals,humidity and temperature at Alert,Nunavut

The effect of pollution-derived sulphuric acid aerosols on wintertime arctic lower atmospheric ice crystals is investigated. These anthropogenic aerosols differ from natural background aerosols by their number concentration, strong solubility and reduced homogeneous freezing temperature when internally mixed with other compounds. Furthermore, observations suggest that the ice-forming nuclei concentration is reduced by one to four orders of magnitude when the sulphuric acid aerosol concentration is high.Simulations performed using a column model and analysis of observed data for the period of 1991–1994 at Alert (82° 30'N, 62°20'W) are used to assess the changes of the boundary layer cloud characteristics by sulphuric acid aerosols and the potential effect on arctic climate. Results show that aerosol acidification leads to depletion of the ice crystal number concentration and an increase of its mean size. As a result, low-level precipitating ice crystals occur more frequently than ice fog and thick nonprecipitating clouds during high concentration of pollution-derived aerosols. This result is in agreement with observations that indicate an increase by more than 50% of the frequency of precipitating ice crystals when the weight proportion of sulphuric acid is greater than its mean value of 20% of the total aerosol mass. Consequently, the ice crystal size increases and number decreases, and the sedimentation flux of ice crystals and the dehydration rate of the lower troposphere are accelerated in the presence of high sulphuric acid aerosol concentration. As a result, the infrared radiation flux reaching the surface and the greenhouse effect are decreased. This process is referred to as the dehydration–greenhouse feedback. One-dimensional simulation for Alert during the period of 1991 to 1994 shows that a negative cloud radiative forcing of −9 W m⁻² may occur locally as a result of the enhanced dehydration rate produced by the aerosol acidity.     

湖北2015年冬季PM2.5重污染过程的气象输送条件及日变化特征分析

PM_2.5污染仍然是湖北省冬季大气污染的首要污染类型,且具有明显区域传输特征,重污染过程的空气污染气象条件有别于华北地区,值得关注。采用WRF/Chem不同排放情景下的模拟结果,并结合观测分析,研究了2015年12月—2016年1月湖北省PM_2.5重污染过程的气象输送条件及日变化特征,从大尺度输送条件和局地边界层动力作用分析了外来污染物水平传输、悬浮聚集和向下传输的过程,并解释了该地区观测到的午后PM_2.5浓度特殊峰值的气象成因。结果表明,湖北重污染爆发以区域传输为主,地面观测PM_2.5极值对应10 m风速可达8—10 m/s,边界层0—1 km为较强偏北风输送,污染传输通量极值位于400 m高度附近,为重要传输通道,低空无明显逆温,重污染过程具有“非静稳”边界层气象特征。重污染形成的大尺度输送条件为,长江中下游及北部地区偏北风异常偏强,南部地区风速减缓,使污染物在中游平原堆积,鄂北边界风速越大,越有利污染输送增长。传输性污染主要来自偏北和东北方向的污染源输送,潜在源区贡献主要为途经偏北通道上的豫中、南阳盆地和关中地区,以及途经东北通道上的鲁、皖、苏等部分地区。PM_2.5浓度日变化双峰结构的天气成因不同,21—24时（北京时）峰值为静稳性污染,11—14时峰值为传输性污染。污染输送受大气边界层高度影响,日出前大气边界层高度较低,层结稳定并伴有上升运行,使得低空外来输送悬浮聚集在400 m高度附近;日出后随大气边界层高度升高,静稳层结被破坏,在干沉降作用下高浓度PM_2.5开始向下传输,并在午后地面形成峰值。      

2004年北京地区秋季大气气溶胶粒子分布特征

2004年秋季在北京地区利用机载大气气溶胶粒子探头进行了大气气溶胶观测,获得了0～7 km气溶胶细粒子数浓度和尺度谱分布的垂直、水平变化特征.结果表明:北京地区上空气溶胶粒子数浓度在1 km左右高度以下的混合层内有均匀的分布,明显递减层的高度范围约在1～2 km之间,2 km以上随高度递减很小,高层气溶胶数浓度变化不大...     

广州地区旱季一次典型灰霾过程的特征及成因分析

通过研究2009年11月广州市气溶胶颗粒物质量浓度(PM10、PM2.5、PM1)、黑碳浓度、散射系数(Scatter)等大气成分要素,以及微波辐射计、激光雷达及风廓线雷达所探测的风、温、湿等边界层结构,统计分析广州旱季一次典型灰霾过程(2009年11月23—29日)中气溶胶颗粒物及其光学特性的时空变化特征,并配合天气形势背景、边界层结构对其形成原因进行详细分析。在典型灰霾过程中,黑碳浓度高达58.7μg/m3,散射系数高达1 902.7 Mm-1,PM10浓度高达423.5μg/m3,PM2.5浓度高达355.7μg/m3,PM1浓度高达286.5μg/m3。通过对同期的气象条件分析表明在广州地区旱季,区域性污染过程,特别是灰霾天气的形成具有以下三种气象条件:大气边界层高度较低;高压变性出海的天气形势与之密切相关;在偏东和偏南气流带来的高湿度环境下,气溶胶吸湿增长效应显著,导致出现严重灰霾天气。     

Spatio-temporal variations of optical properties of aerosols in East Asia measured by MODIS and relation to the ground-based mass concentrations observed in central Korea during 2001∼2010

Long-term variations and trends of atmospheric aerosols in the East Asian region were analyzed by using aerosol optical depth (AOD or τ), and ångström exponent (AE or α) obtained from the Moderate Resolution Imaging Spectroradiometer (MODIS) from 2001 to 2010. The increased emission of anthropogenic fine aerosols in east China resulted in the high AOD in this region during summer. The steady increasing emission of anthropogenic fine aerosols caused an increasing trend of AOD in east China, and the large-scale transport of sandstorms and smoke plume caused by forest fires affected intense inter-annual variations of AOD in the East Asian region. While in the central part of South Korea, located in the lee side of the East Asian continent, AE tended to rise to a level higher than in east China, the ground-based mass concentrations continued to decline. A noticeable decrease of PM10 mass concentration in spring and winter in central Korea is most likely attributable to decreases in sandstorms in the source region of East Asia. However, the ratio of PM2.5 mass concentration to PM10 increases overall with a high level in summer. Aerosol types were classified into dust, smoke plume, and sulphate by using satellite data over Cheongwon in central Korea. The columnar AOD, with different aerosol types, was compared with the ground-based mass concentrations at Cheongwon, and the relatively high level of the correlations presented between PM2.5 and AOD produced in sulphate. Growth and increases of fine hygroscopic aerosols generated as gas-to-particle conversion particularly in summer contribute to increases of columnar AOD in the East Asian region.