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1.
The vertical observation of volatile organic compounds(VOCs) is an important means to clarify the mechanisms of ozone formation. To explore the vertical evolution of VOCs in summer, a field campaign using a tethered balloon during summer photochemical pollution was conducted in Shijiazhuang from 8 June to 3 July 2019. A total of 192 samples were collected, 23 vertical profiles were obtained, and the concentrations of 87 VOCs were measured. The range of the total VOC concentration was 41–48 ppbv below 600 m. It then slightly increased above 600 m, and rose to 58 ± 52 ppbv at 1000 m.The proportion of alkanes increased with height, while the proportions of alkenes, halohydrocarbons and acetylene decreased. The proportion of aromatics remained almost unchanged. A comparison with the results of a winter field campaign during 8–16 January 2019 showed that the concentrations of all VOCs in winter except for halohydrocarbons were more than twice those in summer. Alkanes accounted for the same proportion in winter and summer. Alkenes,aromatics, and acetylene accounted for higher proportions in winter, while halohydrocarbons accounted for a higher proportion in summer. There were five VOC sources in the vertical direction. The proportions of gasoline vehicular emissions + industrial sources and coal burning were higher in winter. The proportions of biogenic sources + long-range transport, solvent usage, and diesel vehicular emissions were higher in summer. From the surface to 1000 m, the proportion of gasoline vehicular emissions + industrial sources gradually increased.  相似文献   

2.
于2016年7月-2017年6月在武汉市典型居民区对大气中101种挥发性有机物（VOCs）进行了监测,以便研究武汉市典型居民区周边VOCs的组成特征和变化规律,并探讨了其主要来源.结果表明,武汉市空气中VOCs的体积分数为（46.24±24.57）×10-9,表现为烷烃>含氧有机物>烯烃>卤代烃>芳香烃.受交通排放影响烷烃的比例上午高于下午,1月机动车尾气为武汉市主要的VOCs排放源,夏季含氧类化合物浓度高于冬季,可能更多地受本地喷涂等溶剂使用行业和光化学反应生成的影响,5-9月表现出明显的生物源排放特征.利用正交矩阵因子分析（PMF）得到武汉市居民区大气VOCs主要有6个来源,分别为燃烧源、机动车尾气、工业排放、溶剂使用、汽油挥发和植物排放.其中,燃烧源、机动车尾气贡献比例最高,是该区域VOCs控制的重要排放源.  相似文献   

3.
PMF和PCA/APCS模型对南京北郊大气VOCs源解析对比研究   总被引：6，自引：0，他引：6  
利用PMF模型和PCA/APCS模型对南京北郊大气VOCs进行定性和定量的源解析,并对比了两种模型的结果。结果表明：PMF模型对不同VOCs种类的模拟效果差别较大,而PCA/APCS对不同VOCs种类的模拟效果相近;PMF模型解析的源个数多于PCA/APCS模型,两种模型结果的源性质方面存在很大相似性,但PCA/APCS模型未能区分汽油挥发和汽车尾气源;两种模型源解析出的植物排放源、工业生产源的贡献率较接近,而其他源的贡献率存在差异,PCA/APCS模型解析的溶剂使用源的贡献率高于PMF模型结果,PMF模型解析出的汽油挥发+汽车尾气源的贡献率高于PCA/APCS模型结果。  相似文献   

4.
Measurements and model developments with the objective to improve the quality and resolution of estimations of anthropogenic emissions are described. Measurement results on a chassis dynamometer were used to determine VOC profiles for exhaust gas emissions of passenger cars for different vehicle and fuel types and different driving modes. Further measurements resulted in emission factors and VOC profiles for lignite burning in residential stoves. Using remote sensing techniques benzene emission factors of gas stations and the efficiency of gasoline vapour recovery systems were measured.To improve the quality and the spatial and temporal resolution of emission data, emission models were improved or modified. This was done by elaborating and applying new methods for important emission source categories (e.g., solvent use, road traffic, small combustion) as well as including new data sources in the calculation routines (e.g. emission statements, land use data, import/export indices of solvents). Simultaneously considerable progress was made improving temporal and spatial allocation functions and VOC profiles. With these improvements a large number of anthropogenic emission data sets for 14 different grid projections in Germany and Europe have been generated. An emission scenario for Germany for 2010 suggests that considering air quality directives from the EU and Germany which are in force or in pipeline, German emissions of VOC and NOx will decrease, but still exceed the national emission ceilings of the EU-NEC directive.  相似文献   

5.
Summer and winter campaigns for the chemical compositions and sources of nonmethane hydrocarbons(NMHCs)and oxygenated volatile organic compounds(OVOCs)were conducted in Xi’an.Data from 57 photochemical assessment monitoring stations for NMHCs and 20 OVOC species were analyzed.Significant seasonal differences were noted for total VOC(TVOC,NMHCs and OVOCs)concentrations and compositions.The campaign-average TVOC concentrations in winter(85.3±60.6 ppbv)were almost twice those in summer(47.2±31.6 ppbv).Alkanes and OVOCs were the most abundant category in winter and summer,respectively.NMHCs,but not OVOCs,had significantly higher levels on weekends than on weekdays.Total ozone formation potential was higher in summer than in winter(by 50%)because of the high concentrations of alkenes(particularly isoprene),high temperature,and high solar radiation levels in summer.The Hybrid Environmental Receptor Model(HERM)was used to conduct source apportionment for atmospheric TVOCs in winter and summer,with excellent accuracy.HERM demonstrated its suitability in a situation where only partial source profile data were available.The HERM results indicated significantly different seasonal source contributions to TVOCs in Xi’an.In particular,coal and biomass burning had contributions greater than half in winter(53.4%),whereas traffic sources were prevalent in summer(53.1%).This study’s results highlight the need for targeted and adjustable VOC control measures that account for seasonal differences in Xi’an;such measures should target not only the severe problem with VOC pollution but also the problem of consequent secondary pollution(e.g.,from ozone and secondary organic aerosols).  相似文献   

6.
As the key precursors of O_3, anthropogenic non-methane volatile organic compounds(NMVOCs) have been studied intensively. This paper performed a meta-analysis on the spatial and temporal variations of NMVOCs, their roles in photochemical reactions, and their sources in China, based on published research. The results showed that both nonmethane hydrocarbons(NMHCs) and oxygenated VOCs(OVOCs) in China have higher mixing ratios in the eastern developed cities compared to those in the central and western areas. Alkanes are the most abundant NMHCs species in all reported sites while formaldehyde is the most abundant among the OVOCs. OVOCs have the highest mixing ratios in summer and the lowest in winter, which is opposite to NMHCs. Among all NMVOCs, the top eight species account for 50%-70% of the total ozone formation potential(OFP) with different compositions and contributions in different areas. In devolved regions, OFP-NMHCs are the highest in winter while OFP-OVOCs are the highest in summer. Based on positive matrix factorization(PMF) analysis, vehicle exhaust, industrial emissions, and solvent usage in China are the main sources for NMHCs. However, the emission trend analysis showed that solvent usage and industrial emissions will exceed vehicle exhaust and become the two major sources of NMVOCs in near future. Based on the meta-analysis conducted in this work,we believe that the spatio-temporal variations and oxidation mechanisms of atmospheric OVOCs, as well as generating a higher spatial resolution of emission inventories of NMVOCs represent an area for future studies on NMVOCs in China.  相似文献   

7.
近些年京津冀地区秋、冬季大气重污染事件频发,工业生产与居民燃煤是大气灰霾污染的重要原因。河北省沙河市是京津冀地区以玻璃制造和加工为主的典型工业城市,本研究选取该城市为研究对象,主要利用2017年1月至12月国控站点的大气环境监测和气象数据,采用扩散模型、潜在源分析等手段,分析了沙河市主要污染物的时空分布特征和污染来源。主要结论有:（1）沙河市首要污染物具有明显季节特征,春季、夏季、秋冬季分别以PM10、O3、PM2.5污染为主,季节贡献率分别为43.3%、72.3%、61.5%。（2）受城市大气边界层和排放的共同影响,PM10、PM2.5、SO2、NO2和CO浓度均有剧烈的季节—日变化特征。（3）冬季东北风时PM2.5、NO2、SO2均展现出高浓度和高相关性特征,表明站点可能受东北方向玻璃企业排放影响。同时,站点可能也受城中村散煤燃烧影响。（4）沙河市冬季PM2.5浓度为143 μg m-3。冬季的一次重污染中硫氧化率SOR、氮氧化率NOR的最高值分别达0.67、0.39,气态污染物的二次转化剧烈,高湿度利于二次粒子的生成。重污染中C(NO3-)/C(SO42-)均值为1.89,推测沙河市NO2主要来自大型运输车辆和企业的共同排放。（5）本地源是沙河市PM2.5的主要潜在源区,周边几个重工业城市也有一定贡献。因此本研究建议沙河市PM2.5的治理除需加强本地污染源的削减和控制外,区域联防联控也十分重要。  相似文献   

8.
In part 3 of this series of papers on a new 3-D global troposphericchemical transport model, using an Integrated Modelling System (IMS), anevaluation of the model performance in simulating global distributions andseasonal variations for volatile organic compounds (VOCs) in the atmosphere,is presented. Comparisons of model OH concentrations with previous modelstudies show consistent modelled OH levels from the subtropics tomidlatitudes, while more discrepancies occur over the tropical lowlatitudes, with IMS predicting the highest levels of OH. The close agreementbetween modelled OH concentrations over midlatitudes, where high surfaceNOxand VOC concentrations are also found, is indicative of the strongphotochemical coupling between NOx, VOCs and O3 overthese latitudes. IMSOH concentrations in the Northern Hemisphere (NH) midlatitudes during summerare generally lower than available measurements, implying that models ingeneral are underestimating OH levels at this location and time of year.Substantial differences between model OH concentrations over low latitudesclearly highlight areas of uncertainty between models. IMS OH concentrationsare the highest in general of the models compared, one possible reason isthat biogenic emissions of species such as isoprene and monoterpenes arehighest in IMS, leading to higher O3 levels and hence higher OH.Generally, the IMS VOC concentrations show a similar seasonality to themeasurements at most locations. In general though, IMS tends to underestimatethe NH wintertime VOC maximum and overestimate the NH summertime VOCminimum. Such an overestimate in summer could be due to IMSunderestimating OH levels, or an overestimation of VOC emissions or possiblya problem with model transport, all of these possibilities are explored.Except for n-pentane, the model underprediction of a VOC maximum during theNH winter month strongly suggests a missing emission mechanism in the modelor an underestimate of an existing one. It is very likely that there is alack of time varying emission sources in the model to account for theseasonal change in emission behaviour such as increasing energy usage (e.g.,electricity and gas), road transportation, engine performance, and otheranthropogenic factors which show strong seasonal characteristics. Theanomalous overprediction of wintertime n-pentane compared with its closesummertime prediction with the measurements suggest that emissions in thiscase may be too high.  相似文献   

9.
Tianjin is the third largest megacity and the fastest growth area in China, and consequently faces the problems of surface ozone and haze episodes. This study measures and characterizes volatile organic compounds(VOCs), which are ozone precursors, to identify their possible sources and evaluate their contribution to ozone formation in urban and suburban Tianjin,China during the Ha Chi(Haze in China) summer campaign in 2009. A total of 107 species of ambient VOCs were detected,and the average concentrations of VOCs at urban and suburban sites were 92 and 174 ppbv, respectively. Of those, 51 species of VOCs were extracted to analyze the possible VOC sources using positive matrix factorization. The identified sources of VOCs were significantly related to vehicular activities, which specifically contributed 60% to urban and 42% to suburban VOCs loadings in Tianjin. Industrial emission was the second most prominent source of ambient VOCs in both urban and suburban areas, although the contribution of industry in the suburban area(36%) was much higher than that at the urban area(16%). We conclude that controlling vehicle emissions should be a top priority for VOC reduction, and that fast industrialization and urbanization causes air pollution to be more complex due to the combined emission of VOCs from industry and daily life, especially in suburban areas.  相似文献   

10.
Volatile organic compounds (VOCs) were measured at two sites in a highly industrialized zone in western Canada from September 2004 to March 2006. Principal component analysis (PCA) with varimax rotation was performed on 30 VOCs to identify the pollution sources. Aliphatics, aromatics, and halogenated aliphatics were studied. The two monitoring sites were 11 km apart, with site 1 closer to the city of Fort Saskatchewan and site 2 predominantly down wind from the industrial sources. PCA results provided the basis for interpreting the relationship between the ambient 24-h integrated VOC samples and the emission sources in the region. Challenges existed in interpreting the PCA results in such a highly industrialized region; however a unique feature to this study was the fact that the region was home to the only 1,2-dichloroethane emitting facility in Canada. Other specific industry related VOCs in the region were vinyl chloride, styrene and HCFC-22. Making use of these specific VOCs in the PCA allowed for easy identification of an industrial contribution. For factors that were not easily distinguishable, further PCA tests were conducted using carbon monoxide concentrations, wind direction data and seasonal splitting of the samples. The analysis found that five factors accounted for 82% of the variance at site 1 and five factors accounted for 81% of the variance at site 2. The factor accounting for the highest variability (∼40%) at the two sites was the most difficult to interpret, but showed contributions from both industry and vehicle related emissions. Specific industrial sources were identified using 1,2-dichloroethane as a chemical tracer or by corroborating wind speed with known industry VOC emissions. Both sites had two factors identified as specific industry sources and these factors totaled to over 20% of the variance. Long range transport of stable halogenated compounds accounted for greater than 10% of the variance, and seasonal effects accounted for 5% of the variance.  相似文献   

11.
Fine aerosol samples were collected throughout spring, summer, and winter in 2004∼2005 at a major urban traffic junction (BNU) and a suburban location (MY) in Beijing and at a downtown site (SH) in Shanghai, China. Ten of the 16 EPA priority polycyclic aromatic hydrocarbons (PAHs), seven fatty acids, levoglucosan, and cholesterol were identified and quantified. PAHs detected in Beijing and Shanghai were up to one order of magnitude higher than those reported in the developed countries either in urban or suburban areas, while levoglucosan was one order of magnitude lower than that in other countries for no biomass combustion in domestic heating in the mega-cities in China. PAHs showed the same seasonal trend in all sampling sites as the highest in winter and the lowest in summer, while fatty acids no pronounced seasonal variation. A significant fraction of levoglucosan from cooking with higher concentrations in urban than in suburban area contributed to the ambient atmosphere, indicating that the main source of levoglucosan in urban environment would be cooking rather than biomass burning. The relative contributions of coal combustion and vehicle exhaust sources to PAHs in fine aerosols were preliminarily estimated to be 1:2 in Beijing and 1:1 in Shanghai, revealing that the air pollution in these mega-cities in China was mainly the mixing of coal combustion with vehicle exhaust. Cooking was one of the major sources of organic aerosols in both Beijing and Shanghai.  相似文献   

12.
We present mobile vehicle lidar observations in Tianjin, China during the spring, summer, and winter of 2016. Mobile observations were carried out along the city border road of Tianjin to obtain the vertical distribution characteristics of PM2.5. Hygroscopic growth was not considered since relative humidity was less than 60% during the observation experiments. PM2.5 profile was obtained with the linear regression equation between the particle extinction coefficient and PM2.5 mass concentration. In spring, the vertical distribution of PM2.5 exhibited a hierarchical structure. In addition to a layer of particles that gathered near the ground, a portion of particles floated at 0.6–2.5-km height. In summer and winter, the fine particles basically gathered below 1 km near the ground. In spring and summer, the concentration of fine particles in the south was higher than that in the north because of the influence of south wind. In winter, the distribution of fine particles was opposite to that measured during spring and summer. High concentrations of PM2.5 were observed in the rural areas of North Tianjin with a maximum of 350 μg m–3 on 13 December 2016. It is shown that industrial and ship emissions in spring and summer and coal combustion in winter were the major sources of fine particles that polluted Tianjin. The results provide insights into the mechanisms of haze formation and the effects of meteorological conditions during haze–fog pollution episodes in the Tianjin area.  相似文献   

13.
We studied the daily patterns in the rates of terpene emissions by the montane holm oak, Quercus ilex, in three typical days of winter and three typical days of summer in Montseny, a natural park near Barcelona, and related them to the air concentrations of terpenes, ozone and NO2. Terpene emission rates were about 10 times higher in summer than in winter. Emissions virtually stopped in the dark. In both seasons, rates of terpene emissions were well correlated with light, air temperature and relative humidity. Rates of emissions were also correlated with stomatal conductance and the rates of transpiration and photosynthesis. Almost all the individual terpenes identified followed the same pattern as total terpenes. The most abundant terpene was ??-pinene, followed by sabinene + ??-pinene, limonene, myrcene, camphene and ??-phellandrene. Atmospheric terpene concentrations were also about 10 times higher in summer than in winter. A significant diurnal pattern with maxima at midday was observed, especially in summer. The increase by one order of magnitude in the concentrations of these volatile isoprenoids highlights the importance of local biogenic summer emissions in these Mediterranean forested areas which also receive polluted air masses from nearby or distant anthropic sources. Atmospheric concentrations of O3 and NO2 were also significantly higher in summer and at midday hours. In both seasons, concentrations of O3 were significantly correlated with concentrations of terpenes and NO2 in the air and with rates of terpene emission.  相似文献   

14.
本文利用气体组分及大气气溶胶在线监测系统(MARGA ADI 2080)观测武汉市2018年1月9—26日大气气溶胶中的8种水溶性离子(NH+4、NO-3、SO2-4、Cl-、K+、Ca2+、Na+和Mg2+),结合气象要素数据,使用主成分分析(PCA)、正定矩阵因子分析法(PMF)、HYSPLIT后向轨迹模式、潜在源区贡献(PSCF)和浓度权重轨迹(CWT),对霾污染过程中水溶性离子进行了全面的来源解析,探究了霾不同阶段下来源差异和空间分布特征。结果表明:(1)本次霾污染中的8种水溶性离子和4种污染气体,PCA解析出的源和占比分别为二次源和燃煤源的混合源(41.28%)、工业排放和土壤扬尘混合源(27.73%)和机动车排放源(9.63%),PMF解析出的源和占比分别为燃煤与土壤扬尘混合源(18.57%)、机动车排放源(20.74%)、二次源(18.30%)、光化学污染源(22.24%)和燃煤源(20.15%)。(2)霾在不同阶段下水溶性离子和4种污染气体的来源存在差异,在清洁天和霾消散阶段,光化学的贡献最高,占比分别为31.42%和36.07%;在霾发生阶段燃煤与土壤扬尘源的贡献最高,其贡献为40.94%;在霾发展阶段,最大的控制源为二次源,贡献占比为37.51%。(3)此次武汉市霾污染中PM2.5浓度和NH+4、NO-3和SO2-4的潜在源区为皖豫鄂三省和赣湘鄂三省交界处。霾污染中PM2.5的主要影响范围是武汉市南部和北部省份,NO-3、NH+4和SO2-4的主要影响区域为武汉市东北方向的城市、湖南省和江西省。  相似文献   

15.
Size-segregated aerosol samples were collected with a low-pressure impactor (LPI) at urban, roadside and rural sites in winter in Beijing. The size distribution of Polycyclic Aromatic Hydrocarbons (PAHs), organic carbon (OC) and elemental carbon (EC) were measured and this study focused on their size distributions and relationships of PAH to OC/EC. All PAHs show uni-modal at the accumulation mode (0.1–1.8 μm) and almost all PAHs are associated with fine particles. The absence of PAHs in the nucleus mode contributes to the coagulation under the condition of high concentration of the accumulation mode particles. The absence of PAHs in the coarse mode was probably attributed to the low temperature that restrained the redistribution of PAHs from the accumulation mode to the coarse mode. Flu(fluoranthene) and Pyr(pyrene, 4-ring) were the most abundant particulate PAHs ; however, IcdP(indeno[1,2,3-cd]pyrene) and BghiP(benzo[ghi]perylene, 6-ring) were rather low. Diagnostic ratios show vehicle and coal burning were the major sources of PAHs in winter. Ratios at rural site are obviously different from those found at roadside and urban sites. Lower value of OC/EC in the rural area than that in the urban area was probably resulted from coal burning prevailed in the rural area. OC1 and OC2 exhibit uni-mode distribution similar to their particle surface area distribution indicating their existence on particles by adsorption. OC3 and OC4 show bi-mode distribution. Grinding of biomass debris can be a probable source of OC3 and OC4 in the coarse mode. EC1 is mostly from the pyrolysis of OC; however, both the natural and anthropogenic emissions contribute to EC2. The correlation between size-segregated PAHs and carbonaceous component is also discussed to identify their sources.  相似文献   

16.
A model of the U.S. automobile market is used to test the role that natural gas vehicles (NGVs) might play in reducing greenhouse-gas emissions. Since natural gas (primarily methane) emits less CO2 per unit of energy than petroleum products, NGVs are an obvious pathway to lower CO2 emissions. High-and low-demand scenarios are used to forecast the emissions from unrestricted growth and a modest program of conservation, respectively. Based on these scenarios, a reference scenario is developed that projects a possible future path of automobile use and efficiency. It is found that without a dramatic increase in automobile use, fuel consumption and greenhouse-gas emissions from automobiles in the United States will probably decrease in the future, provided that efficiency continues to improve at modest rates. In theory, NGVs can help shift emissions even further down.A second objective is to quantify the role that leaking methane might play in offsetting some of the greenhouse advantages of NGVs. To do this, a simple atmospheric chemistry model is applied to the reference scenario; several leak rates and feedback factors are used to test the sensitivity of the projected green-house forcing from now until 2050. Committed warming beyond 2050 is not included, and the results should be interpreted with that in mind.It is highly unlikely that switching automobiles from gasoline to natural gas will appreciably lower future greenhouse forcing. Constraints on vehicle miles travelled as well as continued improvements in vehicle efficiency will make a much larger contribution towards controlling global warming.  相似文献   

17.
南京市降水化学特征及其来源研究   总被引：4，自引：0，他引：4       下载免费PDF全文
为了解南京江北地区降水化学特征,分析了2011年3—6月共25个降水日的109个降水样品中的主要水溶性离子,并利用后向轨迹模式探讨了降水气团来源.结果表明:1)南京地区3—6月降水主要受南、北2种气团影响,北方气团降水的主要离子浓度高于南方气团降水.2)海盐示踪法和相关性分析显示,降水中NO3-和SO42-主要来自燃煤、工业排放和汽车尾气;Ca2+主要来自地壳源;Cl-主要来自海洋;海洋源和陆源对Mg2+和K+都有贡献,Mg2+的陆源贡献大于海洋源贡献,K+受海洋源的影响程度要低于Mg2+.3)南、北气团初期降水的各离子浓度高于总降水的各离子浓度,且初期降水的主要离子的富集系数高于总降水.这说明在降水初始阶段,雨水对南京大气中污染物(气态污染物和颗粒物)的云下冲刷去除作用较强,降水的离子浓度最高,局地源对降水离子的贡献较明显.  相似文献   

18.
The study estimated, for the first time, the greenhouse gas emissions associated with cattle raising in Brazil, focusing on the period from 2003 to 2008 and the three principal sources: 1) portion of deforestation resulting in pasture establishment and subsequent burning of felled vegetation; 2) pasture burning; and 3) bovine enteric fermentation. Deforestation for pasture establishment was only considered for the Amazon and Cerrado. Emissions from pasture burning and enteric fermentation were accounted for the entire country. The consolidated emissions estimate lies between approximately 813 Mt CO2eq in 2008 (smallest value) and approximately 1,090 Mt CO2eq in 2003 (greatest value). The total emissions associated with Amazon cattle ranching ranged from 499 to 775 Mt CO2eq, that of the Cerrado from 229 to 231 Mt CO2eq, and that of the rest of the country between 84 and 87 Mt CO2eq. The full set of emissions originating from cattle raising is responsible for approximately half of all Brazilian emissions (estimated to be approximately 1,055 Mt CO2eq in 2005), even without considering cattle related sources not explicitly estimated in this study, such as energy use for transport and refrigeration along the beef and derivatives supply chain. The potential for reduction of greenhouse gas emissions offered by the Brazilian cattle industry is very high and might constitute Brazil’s most important opportunity for emissions mitigation. The study offers a series of policy recommendations for mitigation that can be implemented by public and private administrators at a low cost relative to other greenhouse gas reduction options.  相似文献   

19.
Diurnal and annual variations of CO2, O3, SO2, black carbon and condensation nuclei and their source areas were studied by utilizing air parcel trajectories and tropospheric concentration measurements at a boreal GAW site in Pallas, Finland. The average growth trend of CO2 was about 2.5 ppm yr−1 according to a 4-yr measurement period starting in October 1996. The annual cycle of CO2 showed concentration difference of about 19 ppm between the summer minimum and winter maximum. The diurnal cycle was most pronounced during July and August. The variation between daily minimum and maximum was about 5 ppm. There was a diurnal cycle in aerosol concentrations during spring and summer. Diurnal variation in ozone concentrations was weak. According to trajectory analysis the site was equally affected by continental and marine air masses. During summer the contribution of continental air increased, although the southernmost influences decreased. During daytime in summer the source areas of CO2 were mainly located in the northern parts of the Central Europe, while during winter the sources were more evenly distributed. Ozone showed similar source areas during summer, while during winter, unlike CO2, high concentrations were observed in air arriving from the sea. Sulfur dioxide sources were more northern (Kola peninsula and further east) and CO2 sources west-weighted in comparison to sources of black carbon. Source areas of black carbon were similar to source areas of aerosols during winter. Aerosol source area distributions showed signs of marine sources during spring and summer.  相似文献   

20.
The leading mode of southern hemisphere (SH) climatic variability, the southern annular mode (SAM), has recently seen a shift towards its positive phase due to stratospheric ozone depletion and increasing greenhouse gas (GHG) concentrations. Here we examine how sensitive the SAM (defined as the leading empirical orthogonal function of SH sea level pressure anomalies) is to future GHG concentrations. We determine its likely evolution for three intergovernmental panel on climate change (IPCC) special report on emission scenarios (SRES) for austral summer and winter, using a multi-model ensemble of IPCC fourth assessment report models which resolve stratospheric ozone recovery. During the period of summer ozone recovery (2000–2050), the SAM index exhibits weakly negative, statistically insignificant trends due to stratospheric ozone recovery which offsets the positive forcing imposed by increasing GHG concentrations. Thereafter, positive SAM index trends occur with magnitudes that show sensitivity to the SRES scenario utilised, and thus future GHG emissions. Trends are determined to be strongest for SRES A2, followed by A1B and B1, respectively. The winter SAM maintains a similar dependency upon GHG as summer, but over the entire twenty-first century and to a greater extent. We also examine the influence of ozone recovery by comparing results to models that exclude stratospheric ozone recovery. Projections are shown to be statistically different from the aforementioned results, highlighting the importance of ozone recovery in governing SAM-evolution. We therefore demonstrate that the future SAM will depend both upon GHG emissions and stratospheric ozone recovery.  相似文献   

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