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1.
徐栋夫  曹萍萍  王源程 《气象》2020,46(7):948-958
利用微脉冲激光雷达观测数据、PM_(2.5)浓度数据、地面气象观测资料和探空数据对成都2017年1月1—6日连续出现的重污染过程进行分析研究。结果表明:激光雷达反演的消光系数演变与PM_(2.5)浓度值变化对应一致,PM_(2.5)浓度升高,近地面消光系数增大;反之,则近地面消光系数减小。对于此次过程,在无冷空气影响时,混合层高度和相对湿度的日变化对消光系数廓线有明显影响,混合层高度降低,大气环境容量减小,相对湿度增加,气溶胶吸湿增长,消光系数增大,地面污染加重。天空状况对气溶胶垂直分布影响显著,晴天或多云天气,早晨强逆温使得水汽和大量气溶胶集中在逆温层顶以下区域,地面污染严重;中午混合层发展,使得混合层内的气溶胶均匀混合,气溶胶层变厚,近地面消光系数显著减小,地面污染减轻。在前一日为晴天或多云天气,当天为阴天时,早上气溶胶明显分为两层,一层在近地面,另一层在残留层顶附近;中午由于垂直湍流增强,一部分残留层气溶胶向下混合至混合层内,使得混合层内的气溶胶粒子增多,地面污染加重,消光系数明显增加。近地面强逆温层、混合层高度降低、残留层气溶胶向下混合、相对湿度增加均是导致地面污染加重的原因。  相似文献   

2.
根据河北邢台市2015年10月11—23日一次重污染天气过程的激光雷达探测数据,对大气污染物浓度和雷达反演得出的大气边界层(PBL)高度、气溶胶光学厚度(AOD)和消光系数的变化进行分析。结果表明:在剔除降水因子的影响后,PBL高度对PM_(2.5)浓度有显著影响,PBL高度越低,PM_(2.5)浓度越高,且两者的相关性夜间好于日间;大气污染物浓度的增加会导致AOD和气溶胶消光系数的显著升高,且AOD与PM_(2.5)浓度的相关性日间好于夜间,在降水的湿沉降效应和大气相对湿度增加的影响下,会出现大气污染物浓度下降,但AOD升高的现象;300 m高度的气溶胶消光系数与地面污染物浓度的日变化趋势较为一致,贴近地面处消光系数相对较小。整体而言,随着PBL高度下降、AOD上升和消光系数增加,环境大气质量逐步趋于恶化。  相似文献   

3.
重度灰霾(或重霾)条件下,大气气溶胶颗粒物显著衰减到达地表的太阳紫外辐射,对臭氧O3光化学过程形成产生重要影响。通过对2013年12月1-10日发生在长三角地区的一次重霾过程进行详尽分析,结合对流层紫外和可见光模型(TUV)及NCAR箱式模型(MM),探讨气溶胶辐射效应对地面臭氧形成和浓度峰值的影响。研究表明,区域输送、稳定边界层累积和二次气溶胶过程等是导致本次重霾发生的主要原因;重霾条件下,臭氧光化学反应明显减弱,臭氧日峰值明显降低,但光化学反应仍缓慢进行;受各种因素如区域输送、边界层累积效应及二次气溶胶等过程影响,臭氧浓度随细颗粒物PM10浓度升高而缓慢上升。TUV和MM模拟结果与观测吻合较好,模拟结果进一步显示,当气溶胶光学厚度AOD由0.8增加到2.0时,到达地表的紫外辐射衰减63%,地面臭氧峰值浓度降低近83%,表明随着灰霾污染加重,近地层臭氧浓度有所降低。  相似文献   

4.
李星敏  陈闯  董自鹏  董妍  杜川利  彭艳 《气象》2018,44(7):929-935
利用西安泾河和长安的气象观测资料、陕西秦岭大气科学试验基地气溶胶粒子谱观测资料及西安市环境保护局颗粒物质量浓度观测资料,分析了气象条件对关中颗粒物粒径谱的影响,结果表明:关中特殊的地形影响和严重的颗粒物污染是霾易发的主要原因;混合层高度与PM_(2.5)质量浓度具有较明显的负相关关系,秋、冬季混合层高度高有利于颗粒物污染的扩散。不同方向上风速变化对颗粒物浓度的影响体现了西北气流对关中颗粒物污染的扩散作用和偏东气流对颗粒物污染的输送。高相对湿度有利于稳定层结的维持和污染物集聚,当相对湿度≤80%时,粒径在150nm~1.0μm的粒子的数浓度,随着相对湿度的增大明显增加,对降低能见度、形成雾-霾有重要作用。不同粒径段粒子的数浓度随相对湿度的变化不同,对能见度的影响也不同;相对湿度越大,湿度对降低能见度的贡献越大。  相似文献   

5.
利用2016年宁波逐时气象观测资料、大气成分监测资料及气溶胶激光雷达资料,对宁波地区霾日进行判定,并对不同天气状况下气溶胶垂直分布特征进行分析。结果表明:2016年宁波地区霾日共70天,轻微霾最多为54天。气象要素和颗粒物浓度在霾日和非霾日都有明显日变化特征,除风速以外,能见度、PM2.5和PM10在霾日和非霾日有非常显著的差异。霾日和非霾日均在高度为0.00.5km时,气溶胶消光系数最大,贡献率分别为53.3%和40.5%。不同季节气溶胶消光系数变化范围有明显差异,消光系数在霾日秋季的>冬季的>春季的;非霾日冬季的>秋季的>春季的>夏季的。秋冬季多冷空气活动,多污染物输送造成霾日消光系数明显高于非霾日的,秋季两者消光系数峰值差异达0.47km^-1。夜间到早晨由于扩散条件不利,容易有污染物的积累增长。春季轻微霾在02时前后消光系数最大,可达2.9km^-1;轻度霾08时在1.4km处的最大,可达2.8km^-1。秋季轻微霾在0.5km以下,02时、08时有消光系数峰值区,最大可达1.0~1.2km^-1。冬季多静稳天气,扩散条件较差,气溶胶消光系数日变化规律不明显,随着霾程度的加重,消光系数波动幅度增大,无霾或轻微霾时消光系数为0.0~1.0km^-1,轻度和中度霾时,消光系数峰值从1.2km^-1增大到2.2km^-1。  相似文献   

6.
2017年12月22日至2018年1月18日利用无人机携带温、湿和颗粒物浓度探测仪对南京地区灰霾污染条件下大气边界层垂直结构开展加密观测。通过比较不同灰霾污染条件下温度、湿度和PM2.5(直径小于2.5微米的颗粒物)浓度的垂直结构差异,结合地面热通量、2米空气温度、相对湿度、风速、风向及主要大气污染物(如臭氧和PM2.5)浓度,定量评估了气溶胶辐射效应对边界层和夹卷过程的影响。分析表明,灰霾或气溶胶削弱到达地表太阳辐射,减小地表感热通量,延迟边界层发展,增加近地层大气稳定度,降低边界层高度,并加重灰霾污染。灰霾污染物在混合层顶处累积,导致PM2.5浓度最大变化出现在边界层顶部而不是近地层。气溶胶辐射效应对夹卷特征及其特征参数有重要影响。灰霾浓度升高时,夹卷区厚度增加;无量纲化夹卷速度随对流理查逊数的变化不再符合负1次方幂函数关系,与大涡模拟结果一致。本研究进一步指出,为提高重霾污染条件下天气和空气质量数值预报水平,必须考虑气溶胶辐射效应对边界层和夹卷参数化的影响。  相似文献   

7.
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   

8.
利用地面激光雷达、太阳光度计观测反演气溶胶光学特性参数,结合PM2.5观测数据,分析了2018年1月25—28日北京一次完整污染过程中气溶胶光学特性变化。基于观测数据,利用短波辐射传输模式计算了不同程度污染日,晴空背景下气溶胶对辐射加热率的改变程度。结果表明:清洁日(25日),PM2.5日平均质量浓度为19.00 μg·m-3,440 nm气溶胶光学厚度为0.13,单次散射反照率为0.87,整层气溶胶消光系数低于0.10 km-1,短波辐射均为增温效应;污染期间(26—27日),PM2.5日平均质量浓度为83.21 μg·m-3,气溶胶光学厚度为2.48,气溶胶散射能力增强,单次散射反照率达到0.94,气溶胶主要消光层厚度提升至3.00 km高度,消光系数平均值为0.43 km-1,气溶胶在垂直方向的变化导致气溶胶中上层(1.50~3.00 km高度)加热作用强烈,短波辐射加热率平均值达到13.89 K·d-1,而低层(1.50 km高度以内)加热作用较弱,加热率平均值仅为0.99 K·d-1。气溶胶散射能力增强导致加热作用减弱,污染日加热率对于气溶胶散射能力变化更敏感。  相似文献   

9.
利用大气观测、探测及污染物探测资料、NCEP再分析资料和GDAS资料,对2013年10月26—29日一次持续性重霾天气过程中的气象要素和气溶胶演变特征进行分析。结果表明:本次持续性霾天气过程中,临沂地区PM_(2.5)污染严重,大气中PM_(2.5)的小时平均浓度工业区城区郊区,污染最严重时分别为365,344,284μg·m~(-3);较小的地面平均风速及PM_(2.5)浓度的稳定上升和较低的地面湿度为本次霾天气过程的形成和发展提供了有利条件;当临沂地区以南风或西南风为主时,市区霾天气加重,上游空气污染具有平流输送特征。贴地逆温层的形成,导致污染物在低空不断积累,造成污染浓度的持续升高。地方政府应加快产业结构调整,控制企业的污染物排放,才是治理雾霾的根本办法。  相似文献   

10.
2012年春季北京经历了罕见的连续污染过程,本研究着眼于霾及沙尘污染事件,对比探讨了两典型污染事件中亚微米细颗粒物(PM_1)化学组分的差异。结果表明:霾事件中,PM_1硝酸盐增长最为明显且所占比重最大,硝酸盐在PM_1浓度迅速增加,其中1质量浓度的平均占比为32.2%,最大可达42%,这与其它季节霾污染特性显著不同,二次无机气溶胶(硝酸盐,硫酸盐,铵盐)增长明显,平均质量浓度为55.1±23.8μg m~(-3),PM_1有机气溶胶所占比重1的质量贡献为66.5%。沙尘污染事件的化学组分特性与霾事件显著不同,最大,PM_1浓度为8.9±5.4μg m~(-3),二次无机气溶胶质量浓度较低,且仅1平均质量贡献为64.0%,平均占PM_1气污染控制策略的制定需依据气溶胶的特点及形成机理有1质量浓度的34.0%。本研究表明,空针对性进行。  相似文献   

11.
The CHIMERE mesoscale chemistry transport model is used for the quantitative assessment of the contribution of transboundary transport of anthropogenic admixtures from China to the surface concentrations of major suspended pollutants, aerosol PM10, ozone O3, and nitrogen oxides NOx in the Far Eastern region. Analyzed in detail are the time series of concentration of mentioned substances computed with the model taking account and not taking account of anthropogenic emissions in China. It is revealed that the transboundary transport of anthropogenic pollutants can cause the recurring episodes of manyfold increase in the concentration of PM10 in the south of Khabarovsk region, as well as more rare variations of O3 and NOx concentration. The trajectory and synoptic analysis demonstrated that the episodes of the increase in the concentration of PM10 and O3 in the south of the region mainly depend on the carryover of air masses from northeastern China in the front part of continental cyclones.  相似文献   

12.
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 PM2.5 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.  相似文献   

13.
对气溶胶气候效应开展分类评估并探讨诊断方法的合理性。人为气溶胶辐射效应对计算云辐射强迫的影响为0.38 W·m~(-2)。诊断评估气溶胶对云辐射强迫的影响需要排除这个偏差。两种基于不同试验设计诊断得出的半直接效应分别为0.21和0.09 W·m~(-2),存在显著差异。主要原因可能是人为气溶胶影响云辐射强迫的不同机制之间在模式模拟过程中不断地相互交织,不是简单的线性叠加关系。模式诊断得出的Twomey效应不仅包括Twomey效应本身,还包括Twomey效应引起的部分快速调整。总之,利用模式评估分析人为气溶胶气候效应需要注意审查试验设计和诊断方法的合理性。  相似文献   

14.
大气污染物排放清单是空气质量模拟和空气污染治理的重要依据.本研究比较分析了两套覆盖江苏省的2017年大气污染物排放清单,即分别由上海市环境科学研究院、江苏省环境科学研究院编制的"长三角清单"和"江苏省清单",并结合区域空气质量模型CMAQ评估不同清单对长三角地区2017年1、4、7、10月的空气质量模拟的影响.清单比较结果表明,除二氧化硫(SO2)以外,江苏省清单估算的各污染物排放量较长三角清单低.通过与观测数据比较,发现两套清单对SO2、氮氧化物(NOx)、臭氧(O3)和细颗粒物(PM2.5)的模型模拟性能均较好.江苏省清单与长三角清单两者的模拟结果空间分布接近,其中江苏省清单模拟的PM2.5和O3在长三角多数地区略低于长三角清单的模拟结果(1月O3除外).江苏省清单与长三角清单均能够用于空气质量模式模拟,可为江苏地区的细颗粒物和光化学烟雾污染的控制策略制定提供参考.  相似文献   

15.
北京不同区域气溶胶辐射效应   总被引:1,自引:0,他引:1       下载免费PDF全文
采用大气辐射传输模式SES2以及2013年1月—2015年10月欧洲中期天气预报中心细网格再分析资料计算了北京地区4个观测站地面接收的短波辐射通量,分析了晴天和云天北京城郊气溶胶对总辐射的定量影响时空变化特征。结果表明:北京城区和近郊区气溶胶对总辐射的影响约为远郊区的2倍,北京南部和西部气溶胶对辐射的影响较大,晴天和云天北京城区和近郊区气溶胶对总辐射的削减值分别为146.23~180.99 W·m-2和202.11~217.02 W·m-2,晴天总辐射削减空间差异较大;秋冬季气溶胶对总辐射的影响明显大于春夏季,北京市观象台秋冬季气溶胶对总辐射的削减作用最大可达60%,较春夏季高10%~20%;北京城郊总辐射和直接辐射削减率与气溶胶光学厚度变化均呈线性关系,近地面PM2.5浓度对辐射的影响不容忽视。  相似文献   

16.
Due to increased aerosol emissions and unfavorable weather conditions, severe haze events have occurred frequently in China in the last 10 years. In addition, the interaction between the boundary layer and the aerosol radiative effect may be another important factor in haze formation. To better understand the effect of this interaction, the aerosol radiative effect on a severe haze episode that took place in December 2013 was investigated by using two WRF-Chem model simulations with different aerosol configurations. The results showed that the maximal reduction of regional average surface shortwave radiation, latent heat, and sensible heat during this event were 88, 12, and 37 W m–2, respectively. The planetary boundary layer height, daytime temperature, and wind speed dropped by 276 m, 1°C, and 0.33 m s–1, respectively. The ventilation coefficient dropped by 8%–24% for in the central and northwestern Yangtze River Delta (YRD). The upper level of the atmosphere was warmed and the lower level was cooled, which stabilized the stratification. In a word, the dispersion ability of the atmosphere was weakened due to the aerosol radiative feedback. Additional results showed that the PM2.5 concentration in the central and northwestern YRD increased by 6–18 μg m–3, which is less than 15% of the average PM2.5 concentration during the severely polluted period in this area. The vertical profile showed that the PM2.5 and PM10 concentrations increased below 950 hPa, with a maximum increase of 7 and 8 μg m–3, respectively. Concentrations reduced between 950 and 800 hPa, however, with a maximum reduction of 3.5 and 4.5 μg m–3, respectively. Generally, the aerosol radiative effect aggravated the level of pollution, but the effect was limited, and this haze event was mainly caused by the stagnant meteorological conditions. The interaction between the boundary layer and the aerosol radiative effect may have been less important than the large-scale static weather conditions for the formation of this haze episode.  相似文献   

17.
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.  相似文献   

18.
北京秋季一次典型大气污染过程多站点分析   总被引:3,自引:1,他引:2  
多站点多种大气污染物的同步在线观测对深入剖析大气污染的成因和演变机制有重要意义。以龙潭湖、北京325 m塔、双清路和阳坊4监测站点实时NOx、SO2、O3、PM2.5和PM10浓度观测数据为基础,介绍了北京地区2010年10月3~11日发生的一次典型污染过程。不同污染物在污染过程中变化特征不一致,表现为NOx、SO2、O3浓度有明显日变化,而PM浓度升高后一直维持在高值,日变化幅度很小。通过分析不同站点、相同污染物之间的相关性和变异系数发现,4站点间一次污染物NO和SO2空间浓度差别大,变异系数分别为77%和70%,相关系数低于0.44;而二次污染物NO2、PM2.5、O3空间浓度差别较小,变异系数分别为34%、36%和29%,相关系数均超过0.54。结合中尺度气象模式研究发现,该污染过程中,850 hPa高空持续的西南暖平流造成华北地区显著平流逆温,与近地层辐射逆温共同作用,使北京地区混合层高度维持在1200 m以下。低混合层高度和低风速限制了大气垂直和水平扩散,造成北京地区近地层污染物累积,形成重度污染。  相似文献   

19.
Summary In July 2000 (South Hemisphere winter), the Christchurch Air Pollution Study (CAPS2000) was performed in order to establish a comprehensive data set for documentation and analysis of nocturnal winter smog conditions in the Christchurch area. Field activities included meteorological surface measurements, tethersonde ascents, radiosoundings and sodar measurements. Air pollutant monitoring included CO, NO, NOx, O3, PM10, PM2.5, and black carbon measurements near the surface, and for the first time vertical CO-profile measurements in the nocturnal boundary layer up to 100 m height. A prerequisite for nocturnal winter smog conditions is the evolution of stable stratification before the evening traffic and domestic heating reach a maximum. When stable stratification persists during domestic heating and road traffic in the morning, a second pronounced maximum of air pollutants evolves at around 0800 NZST. The meteorological measurements also revealed a complex nocturnal surface wind field, dominated by drainage winds from the Port Hills to the south and from the Canterbury Plains to the west of the Christchurch city area. A resulting convergence zone forms over the central parts of the city and is accompanied by low wind speeds. The position of the convergence zone varies during the night. These low winds over the city centre, in conjunction with stable stratification, favour the accumulation of air pollutants in the lowest tens of metres. The nocturnal winter smog situation ends with the erosion of the surface inversion at about 1100 NZST. It is shown from analysis of the vertical CO profiles that the level of air pollution in the Christchurch area depends on the height of the stable nocturnal boundary layer, which itself is governed by variations in the local wind systems.  相似文献   

20.
Emissions may affect climate indirectly through chemical interactions in the atmosphere, but quantifications of such effects are difficult and uncertain due to incomplete knowledge and inadequate methods. A preliminary assessment of the climatic impact of changes in tropospheric O3 and CH4 in response to various emissions is given. For a 10% increase in the CH4 emissions the relative increase in concentration has been estimated to be 37% larger. The radiative forcing from enhanced levels of tropospheric O3 is estimated to 37% of the forcing from changes in CH4. Inclusion of indirect effects approximately doubles the climatic impact of CH4 emissions. Emissions of NOx increase tropospheric O3, while the levels of CH4 are reduced. For emissions of NOx from aircraft, the positive effects via O3 changes are significantly larger than the negative through changes in CH4. For NOx emitted from surface sources, the effects through changes in O3 and CH4 are estimated to be of similar magnitude and large uncertainty is connected to the sign of the net effect. Emissions of CO have positive indirect effects on climate through enhanced levels of tropospheric o3 and increased lifetime of CH4. These results form the basis for estimates of global warming potentials for sustained step increases in emissions.  相似文献   

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