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1.
基于2008年9月—2010年9月河北固城生态与农业气象试验站多轴差分吸收光谱仪 (multi-axis differential optical absorption spectroscopy, MAX-DOAS) 获得的太阳散射光谱观测,反演计算该地区NO2对流层柱浓度,分析其季节、日变化特征以及不同来源输送的影响,并与同期NO2地面观测资料和卫星产品进行对比分析。发现固城站NO2对流层柱浓度冬高 (5.14×1016 cm-2) 夏低 (1.28×1016 cm-2);日变化形态在四季均呈现中午低、傍晚高的特征,且冬季最明显。与北京城市区域同期的观测相比,冬季固城站观测值略低,而在春、夏季则偏低较显著。地面风玫瑰图分析显示,来自SW, SSW, NE方向及ENE方向的污染输送对其贡献最大。与地面、卫星NO2观测的对比表明,MAX-DOAS反演的NO2柱浓度与地面观测浓度具有一致的季节和日变化特征,卫星反演的NO2对流层柱浓度产品在华北平原农村地区存在系统性低估。  相似文献   

2.
李蔚  马建中  郭军让 《气象科技》2013,41(5):796-802
介绍了以太阳散射光为光源的多轴差分吸收光谱技术（Multi-Axis Differential Optical Absorption Spectroscopy,简称MAX-DOAS）,以及MAX-DOAS仪器试验应用.试验中选取中午仪器测量的天顶散射光光谱为参考光谱即Fraunhofer参考光谱,并将测量光谱进行消噪、波长校准以及去除Fraunhofer结构处理.利用分子吸收光学厚度和Ring效应光学厚度对处理后的测量光谱进行最小二乘法拟合,反演出了大气NO2差分斜柱浓度（Differential Slant Column Densities,简称DSCD）.分析了天津武清NO2的差分斜柱浓度反演结果,用简单快捷的几何法将NO2差分斜柱浓度转化成对流层垂直柱浓度（Vertical Column Densities,简称VCD）.研究表明,MAX-DOAS可以有效地监测污染地区对流层NO2的垂直柱浓度.  相似文献   

3.
利用景德镇温室气体监测站CO_2观测数据,分析了景德镇地区2017年12月—2018年11月大气CO_2浓度变化特征,同时对其浓度进行了筛分,以剔除污染数据,使其更具区域代表性。研究表明:景德镇地区大气CO_2浓度昼降夜升,早上最高,傍晚最低;春季最高,秋季最低;春、夏季NNE、NE、ENE风向,秋季NE、ENE风向以及冬季W、WSW、SW、SSW、S风向上CO_2浓度较高。同时,春、夏和秋季大气CO_2浓度大致随风速的增加而不断降低,冬季风速对大气CO_2浓度无明显影响。筛分后数据显示景德镇地区年均大气CO_2浓度为422.1×10~(-6),浓度日均值年振幅73.96×10~(-6),夏半年CO_2浓度低于冬半年。  相似文献   

4.
在“双碳”目标背景下，从国家层面到地方层面，区域、城市、行业企业都在制定和实施双碳目标行动计划。CO2模拟因其客观性和高时空分辨率等优势，在城市碳排放研究中深受重视。本研究以京津冀地区为研究区域，采用Picarro仪器高精度观测的2019—2020年CO2数据，利用WRF模式进行CO2传输模拟，分析了CO2浓度变化的季节特征，评估了模式在城区中心、城郊及背景3个观测站点的模拟效果，并对边界层高度及化石燃料碳排放等可能影响CO2浓度的因素进行了研究。3个观测站点分别为北京中国科学院大气物理研究所325 m气象塔观测站（北京站）、河北香河观测站（香河站）和上甸子区域本底观测站（上甸子站）。模拟结果表明：上甸子站优于香河站，香河站优于北京站，在冬季尤其明显；CO2浓度的高值区主要分布在城区、电厂和工业区，尤其是唐山、石家庄和邯郸地区，大量交通、工业排放导致CO2浓度明显上升，且高值区的范围在冬季最大；就日平均变化和日变化而言，边界层高度与CO2浓度存在相反变化趋势；3个站点的化石燃料碳排放（FFECO2）与近地面总CO2浓度存在正相关关系，冬春季的相关性高于夏秋季，且FFECO2的占比从大到小依次为北京站、香河站、上甸子站；CO2传输模拟的不确定性存在空间差异和季节变化。  相似文献   

5.
为了解香河地区气溶胶尺度谱的基本特征,自2012年5月起,利用扫描电迁移率粒径谱仪(SMPS)对河北香河地区的亚微米(13.8~723.4 nm)气溶胶尺度谱分布进行了近2 a的测量。基于该数据集,分析了气溶胶尺度谱的季节变化和日变化特征及气象要素对气溶胶浓度的影响。结果发现,观测期间埃根核模态(20.0~100.0 nm)、积聚模态(100.0~723.4 nm),以及总的气溶胶数浓度、表面积浓度和体积浓度均值分别为7.0×103cm~(-3)、7.5×103cm~(-3)、14.9×103cm~(-3)、1125μm2·cm~(-3)和50μm~3·cm~(-3)。香河地区积聚模态的粒子数浓度接近华北地区其他污染测站的结果,但高于发达国家的测值。冬季气溶胶的平均浓度最高(18.1×10~3cm~(-3)),而春季最低(12.3×10~3cm~(-3))。不同季节,气溶胶的数谱分布主要为单峰分布,平均峰值直径约为105 nm。气溶胶浓度的日变化受机动车排放的影响显著,存在早晚两个高值中心,分别出现在早上的06:00—09:00和晚上的19:00—21:00。风速、风向对气溶胶数浓度的影响较大,低风速(2 m/s)和南风条件,尤其是吹西南风时,气溶胶浓度的增加显著。  相似文献   

6.
用中尺度数值天气模式 Weather Research and Forecasting Model（WRF v32）对2006年中国地区1、4、7、10月4个月（分别对应冬、春、夏、秋）近地层气象要素进行模拟。并利用通榆、榆中和上海站的观测资料对模拟结果进行对比分析。结果表明：WRF模式能较好的模拟出各气象要素的变化特征。但是,各个季节的模拟效果并不相同。在半干旱的通榆和榆中两站,有关要素秋季的模拟最好,夏季较差。在上海站,夏秋两季比较差,冬春两季较好。对温度的模拟,上海站4个季节都偏低,通榆站夏季偏低,冬季偏高。 对风速的模拟,通榆和榆中两站（通榆秋季除外）都偏低,上海站（夏季除外）都偏高。对感热通量和潜热通量的模拟,通榆站夏季感热通量偏大,潜热通量偏小,榆中站夏季感热通量和潜热通量的模拟值都偏大。  相似文献   

7.
利用2018年10月~2020年12月彭州边界层铁塔的风速风向观测资料,分析了彭州地区近地面各季节平均风速日变化、盛行风向及污染系数特征,在此基础上,选取彭州大风天气个例,对按月分类法和风速区间法的反演结果进行了有效性验证。结果表明:除夏季10m高度盛行西风以外,其余三季各高度均盛行东北风,秋冬两季各高度东北风出现频率大于春夏两季,每个季节随着高度增加,东北风出现频率均逐渐增大,对应平均风速均逐渐增大。春夏季10m高度的最大污染系数在偏西方向,其他各高度最大污染系数均在东北方向,各层高度最小污染系数多在东南或偏南方向;秋冬季各高度污染系数均大于春夏季,最大均为东北方向,10~20m最小污染系数多在偏南或偏东南方向,60~90m最小污染系数为偏西北方向;彭州铁塔偏西和东北方向不宜布设污染源。两种风速反演方法均能对近地面风速进行较为有效的反演,风速区间法在大风区间的反演效果优于按月分类法。   相似文献   

8.
北京及其周边地区冬季SO2的变化与输送特征   总被引：4，自引：1，他引：3  
利用实施北京市奥运空气质量保障计划"北京市与周边地区空气污染物的输送、转化及北京市空气质量目标研究"项目的有利时机,于2007年1月15～27日在中国科学院大气物理研究所北京站、香河站和兴隆站,采用先进的差分吸收光谱仪(DOAS)和SO2气体分析仪取得了高质量SO2浓度的连续观测资料,同时还获取了相应的常规气象资料和系留气艇探测的常规气象参数廓线资料.分析和讨论了北京及其周边地区的SO2污染的变化过程特征、日变化特征、输送特征、源排放特征以及与天气过程和气象条件的紧密联系.研究表明:1)北京站、香河站和兴隆站的SO2浓度逐日变化明显,变化趋势一致,通常处于同一个天气系统控制之下,SO2污染呈现区域性分布特征.2)冬季SO2浓度日变化明显,夜晚最高,15时(北京时)最低.3)SO2浓度与大气稳定度、风速、风向密切相关,风速越小、大气越稳定,SO2浓度越高;当吹西南风时,SO2浓度升高,西北风时浓度明显降低.4)HYSPLIT后向轨迹数值模拟结果和OMI卫星反演表明周边地区的SO2长距离输送对站点的贡献不能忽视.  相似文献   

9.
利用2014—2017年华南沿海及南海的浮标站、海岛站、石油平台站、沿海自动站等277个自动站风场数据,与ASCAT反演风场进行了对比分析。结果表明,当观测风速小于5 m/s(大于15 m/s)时,ASCAT反演风速的平均绝对误差在3 m/s左右(存在2级左右的高(低)估);当风速介于5~10 m/s时,平均绝对误差在2 m/s左右(多数ASCAT有1~2级的高估);介于10~15 m/s时,ASCAT反演结果相对最好,风速、风向准确率能够达到60%以上。ASCAT对风速的反演结果受陆地影响较大,与观测风速的相关系数从高到低可分为三类:(1)浮标、平台站;(2)西沙、南沙自动站;(3)广东沿海自动站及海岛站、海南海岛站。ASCAT反演风场在风向的应用较风速更优,其中,东北风样本数最多,其次分别为西南风、东南风和西北风。浮标站、平台站、西沙自动站的风向反演质量相对较好;所有测站风向偏差主要由5 m/s以下的弱风贡献。单站多年月平均风速变化显示,ASCAT反演风速相对测站主要为正偏差,且秋冬季比春夏季偏差更大,这可能与大气稳定度有关。   相似文献   

10.
基于2005—2013年臭氧监测仪(OMI)遥感反演对流层NO2垂直柱浓度资料,分析珠江三角洲地区(简称珠三角)城市群及其相邻区域NO2的时空分布特征及变化趋势,并探究人类活动对NO2的影响。与地面观测数据对比检验显示,OMI遥感NO2资料可靠性较高。研究发现,珠三角城市地区由于工业生产活跃、汽车拥有量高、能源和电力消费量大,相应的化石能源消耗量大,这导致该地区对流层NO2柱浓度平均值(7.4×1015 molec/cm2)约为相邻地区的3倍。与此同时,珠三角地区NO2高污染区域连成一片,城市群效应显著。正弦模型能较好地拟合珠三角及相邻地区NO2的周期性变化特征,NO2浓度高值均出现在冬季,低值出现在夏季。近9年珠三角地区NO2浓度呈下降趋势,与其第二产业产值和汽车拥有量呈较显著的负相关,这表明珠三角地区对氮氧化物排放的治理初见成效。粤东和粤北地区NO2浓度增长趋势显著,与第二产业产值和汽车拥有量存在较好的正相关性,可见工业排放和汽车尾气是这些地区NO2的重要污染源。粤西地区NO2浓度基本不变。   相似文献   

11.
For the measurement of atmospheric NO2 vertical column density (VCD), Kitt Peak Solar Flux Atlas can be substituted as an extraterrestrial solar radiation. Compared with differential analysis method, the Taylor expansion of integrated transfer equation underestimates the VCD. This underestimation is as large as 35% when the amount of NO2 is 1 × 1017 cm－2 and observation is conducted with an air mass factor of 10. Even when the VCD is 2 × 1016 cm－2 and the air mass factor is 4, the relative error of the retrieved VCD is still no less than 3%. If the observation is restricted under the small air mass factor condition (≤4), with Kitt Peak Solar spectrum as an extraterrestrial solar radiation, only an atmospheric layer of 2 km thick from ground can be studied, which will make the absorption too weak to be detected by normal instruments.The VCD in winter Tokyo area was observed and analyzed by differential method, which shows a good precision even when the absorption is as low as 3%. The largest average VCD was about 1.3 × 1017 cm－2, and the lowest was about 1.3 × 1016 cm－2. The trend of its variation was almost the same as the ground level observation by Saltzman reagent method.  相似文献   

12.
NO2的光解速率j(NO2)是对流层化学研究中的一个重要的参数，它是对流层臭氧（O3）和OH自由基的形成关键影响因子之一。本文利用香河站2017年11月至2018年1月的观测资料对NO2的光解速率j(NO2)、太阳辐射的变化特征，及光解速率与分波段辐射相关性进行分析，在此基础上建立了一套适合于构建香河地区j(NO2)的参数化方案。结果表明，香河地区的j(NO2)与太阳辐射的变化趋势基本一致，日变化均呈正午高、早晚低的单峰型。香河地区冬季j(NO2)的变化范围是0.00046～0.0044 s-1，平均值为0.0029 s-1。j(NO2)与晴空指数（KS）和定义的紫外辐射晴空指数（KUV）存在很好的相关性，因此，利用j(NO2)与大气质量数和晴空指数的相互依赖关系，基于KUV构建了适合于香河地区j(NO2) 的估算方程。由于总辐射是气象站的常规观测要素，晴空指数KS更容易获取，继而建立了通过KS参数化计算j(NO2)的估算方程。利用KUV和KS建立的j(NO2)估算方程的瞬时估算值与观测值的平均相对误差分别为6.5%和13.9%，均方根误差分别为0.00029和0.00051。  相似文献   

13.
A programme of ground-based stratospheric and total NO2 column measurements was instituted at the Laboratory of Atmospheric Physics (40.5° N, 22.9° E) in August 1985. We present here the results of the first two years of measurements with a modified Canterbury filter photometer, details of which are given in the text. The stratospheric NO2 column, obtained at twilight during low local NO2 levels, shows the seasonal variation with monthly mean values of about 6×10-15 molec. cm-2 in the summertime to about 2.2×10-15 molec. cm-2 in the wintertime. These measurements compare well with measurements obtained with different instruments by other groups at similar latitudes (about 40° N) but in different places. Also, the asymmetry of the evening-to-morning stratospheric NO2 over Thessaloniki was found to be on the average equal to 1.58. Total NO2 column over Thessaloniki has a pronounced seasonal variation with amplitude of 0.68 matm. cm which can be explained partly from measured local NO2 sources which discharge in the mixing layer and partly from photolysis of the NO2 reservoir species.  相似文献   

14.
气候变化引起的地面气溶胶浓度变化与区域空气质量密切相关。本文利用“国际大气化学—气候模式比较计划”（Atmospheric Chemistry and Climate Model Intercomparison Project, ACCMIP）中4个模式的试验数据分析了RCP8.5情景下2000~2100年气候变化对中国气溶胶浓度的影响。结果显示,在人为气溶胶排放固定在2000年、仅考虑气候变化的影响时,2000~2100年气候变化导致中国北部地区（31°N~45°N, 105°E~122°E）硫酸盐、有机碳和黑碳气溶胶分别增加28%、21%和9%,硝酸盐气溶胶在中国东部地区减少30%。气候变化对细颗粒物（PM2.5）浓度的影响有显著的季节变化特征,冬季PM2.5浓度在中国东部减少15%,这主要是由硝酸盐气溶胶在冬季的显著减少造成的;夏季PM2.5浓度在中国北部地区增加16%,而长江以南地区减少为9%,这可能与模式模拟的未来东亚夏季风环流的增强有关。  相似文献   

15.
大气臭氧变化在全球气候和环境中具有重要作用,是当今大气科学领域的重要研究对象之一。对比分析了中国科学院大气物理研究所河北香河大气综合观测试验站2014～2016年Dobson和Brewer两种臭氧总量观测仪器探测结果的一致性,并使用1979～2016年Dobson观测数据分析了香河地区臭氧总量的长期变化趋势。结果表明:进行有效温度修正后,两种臭氧总量仪器观测结果一致性较好,平均偏差仅为-0.14DU(多布森单位),平均绝对偏差为8.00 DU,标准差为36.09 DU,相关系数达0.964。整体来说,两类仪器观测臭氧总量吻合较好。SO2浓度对Dobson仪器数据精度有一定影响,两组仪器数据在SO2浓度为0～0.2DU、0.2～0.4DU和0.4DU大气条件情况下的平均偏差分别为4.8 DU、7.0 DU和8.0 DU,平均偏差随SO2浓度升高而增大。过去38年香河地区的臭氧总量季节差异性强,春、冬两季臭氧总量高,夏、秋两季臭氧总量相对低,季节变化趋势差异明显。从长期变化上看,臭氧总量变化波动有不同的周期,在4个大的时间段变化趋势不同,2000～2010年臭氧层有显著恢复,但最近几年又有变薄的趋势。  相似文献   

16.
A photochemical box model is used to simulate seasonal variations in concentrations of sulfur compounds at latitude 40° S. It is assumed that the hydroxyl radical (OH) addition reaction to sulfur in the dimethyl sulfide (DMS) molecule is the predominant pathway for methanesulfonic acid (MSA) production, and that the rate constant increases as the air temperature decreases. Concentration of the nitrate radical (NO3) is a function of the DMS flux, because the reaction of DMS with NO3 is the most important loss mechanism of NO3. While the diurnally averaged concentration of OH in winter is a factor of about 8 smaller than in summer, due to the weak photolysis process, the diurnally averaged concentration of NO3 in winter is a factor of about 4–5 larger than in summer, due to the decrease of DMS flux. Therefore, at middle and high latitudes in winter, atmospheric DMS is mainly oxidized by the reaction with NO3. The calculated ratio of the MSA to SO2 production rates is smaller in winter than in summer, and the MSA to non-sea-salt sulfate (nssSO4 2-) molar ratio varies seasonally. This result agrees with data on the seasonal variation of the MSA/nssSO4 2- molar ratio obtained at middle and high latitudes. The calculations indicate that during winter the reaction of DMS with NO3 is likely to be a more important sink of NOx (NO+NO2) than the reaction of NO2 with OH, and to serve as a significant pathway of the HNO3 production. If dimethyl sulfoxide (DMSO) is produced through the OH addition reaction and is heterogeneously oxidized in aqueous solutions, half of the nssSO4 2- produced in summer may be through the oxidation process of DMSO. It is necessary to further investigate the oxidation products by the reaction of DMS with OH, and the possibility of the reaction of DMS with NO3 during winter.  相似文献   

17.
Continuous weekly monitoring on the concentration of gases and aerosols in urban ambient air by a four-stage filter-pack method was carried out for 7 years in order to study not only the acid-base balance of acid-related (HNO3, NO3 −, and non-sea-salt-(nss-)SO4 2−) and alkali-related (NH3, NH4 +, and nss-Ca2+) chemical species but also its influence on the acidification of precipitation. The concentrations of the total nitrate (= NO3− + HNO3) and nss-SO42− showed a similar seasonal variation: high in the summer and low in the winter. The total nitrate and nss-SO42− accounted for 0.43 and 0.57 of the acid-related species, respectively, on an equivalent basis. The total ammonium (= NH3 + NH4+) accounted for more than 0.9 of the alkali-related species, except for a springtime nss-Ca2+ episodic peak. The alkali-related species were generally overabundant compared with the acid-related species in the HNO3-NO3−-nss-SO42−-NH3-NH4+-nss-Ca2+ system. The alkali-rich distribution was especially pronounced in the winter, but the acid-related species was comparable to the alkali-related species in the summer, which was attributed to the larger H+ deposition by precipitation in the summer. This study can provide a methodology to associate survey results obtained by a filter-pack method with those of precipitation.  相似文献   

18.
Methane(CH4) is one of the most important greenhouse gases in the atmosphere, making it worthwhile to study its temporal and vertical distributions in source areas, e.g., North China. For this purpose, a ground-based high-resolution Fourier transform infrared spectrometer(FTIR), the Bruker IFS 125 HR, along with an in-situ instrument, the Picarro G2301, were deployed in Xianghe County(39.8°N,117.0°E), Hebei Province, China. Data have been recorded since June2018. For the FTIR measurements, we used two observation modes to retrieve the mole fraction of CH4: the Total Carbon Column Observing Network(TCCON) method(retrieval algorithm: GGG2014), and the Network for the Detection of Atmospheric Composition Change(NDACC) method(retrieval algorithm: SFIT4). Combining FTIR with in-situ measurements, we found the temporal and vertical distributions of atmospheric CH4 within three vertical layers(near the ground, in the troposphere, and in the stratosphere), and throughout the whole atmosphere. Regarding the diurnal variation of CH4 near the ground, the concentration at night was higher than during the daytime. Regarding the seasonal variation,CH4 was low in spring and high in summer, for all three vertical layers. In addition, there was a peak of CH4 in winter near the ground, both in the troposphere and the whole atmosphere. We found that variation of CH4 in the tropospheric column was close to that of the in-situ measurements near the ground. Furthermore, the variations of CH4 in the stratospheric column could be influenced by vertical motions, since it was higher in summer and lower in winter.  相似文献   

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