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1.
The characteristics of surface O3 on clear days at Waliguan Observatory,Lin'an regional station and Longfengshan regional station in China were analyzed in this paper.The three stations belong to Global Atmospheric Watch(GAW)of WMO.There was obvious daily variation on clear days at Lin'an.with maximum(42.9 ppb)and minimum(20.3 ppb)of daily range appearing in spring and summer,respectively.The daily variation was more regular at Lonfengshan than at Lin'an.The maximum(about 27 ppb)appeared in autumn at Longfengshan.There was no obvious daily variation and also daily range was smaller in other seasons except weaker daily variation in summer at Waliguan.But the surface O3 concentration(SOC)in summer was higher than that in winter at Waliguan.The SOC on clear days of summer at Waliguan was over 20 ppb higher than at Longfengshan and Lin'an.The global radiation and NOx concentration were the main factors which control the SOC on clear days at Longfengshan and Lin'an.and played important role in different seasons and areas.The transportation of air flow around the area of Qinghai-Xizang(Tibet)Plateau was the main cause for high SOC and weak daily variation in summer at Waliguan.The similar effect of transportation was obtained at the Mauna Loa Observatory.The distribution characteristics of SOC increasing with height in the troposphere determined the difference of SOC between East China and West China.  相似文献   

2.
During the BERLIOZ field phase on 20 July 1998 a 40 km wide ozone-plume 30 to 70 km north of Berlin in the lee of the city was detected. The ozone mixing ratio inside the plume was app. 15 ppb higher than outside, mainly caused by high ozone precursor emissions in Berlin, resulting in a net chemical ozone production of 6.5 ppb h–1, which overcompensates ozone advection of –3.6 ppb h–1 andturbulent diffusion of –1.1 ppb h–1. That means, although moreozone leaves the control volume far in the lee of Berlin than enters it at the leeside cityborder and although turbulent diffusion causes a loss of ozone in the leeside control volume the chemical production inside the volume leads to a net ozone increase. Using a semi-Lagrangian mass budget method to estimate the net ozone production, 5.0 ppb h–1 are calculated for theplume. This means a fraction of about 20% of ozone in the plume is producedby local emissions, therefore called `home made' by the Berlin emissions. For the same area KAMM/DRAIS simulations using an observation based initialisation, results in a net production rate between 4.0 and 6.5 ppbh–1, while the threefold nested EURAD model gives 6.0 ppbh–1. The process analysis indicates in many cases goodagreement (10% or better) between measurements and simulations not only in the ozone concentrations but also with respect to the physical and chemical processes governing the total change. Remaining differences are caused by different resolution in time and space of the models and measurements as well as by errors in the emission calculation.The upwind-downwind differences in PAN concentrations are partly similar to those of ozone, because in the BERLIOZ case they are governed mainly by photochemical production. While in the stable boundary layer at night and windward of Berlin 0.1 to 0.3 ppb are detected, in the centre of the plume at noon concentrations between 0.75 ppb and 1.0 ppb are measured. The O3/PAN ratio is about 80 to 120 and thus due to the relatively lowPAN concentrations significantly higher than found in previous studies. The low PAN formation on 20 July, was mainly restricted by the moderate nonmethane hydrocarbon levels, whereas high PAN concentrations of 3.0 ppb on 21 July, are caused by local production in the boundary layer and by large scale advection aloft.  相似文献   

3.
The characteristics of surface O_3 on clear days at Waliguan Observatory,Lin'an regionalstation and Longfengshan regional station in China were analyzed in this paper.The three stationsbelong to Global Atmospheric Watch(GAW)of WMO.There was obvious daily variation on cleardays at Lin'an.with maximum(42.9 ppb)and minimum(20.3 ppb)of daily range appearing inspring and summer.respectively.The daily variation was more regular at Lonfengshan than atLin'an.The maximum(about 27 ppb)appeared in autumn at Longfengshan.There was noobvious daily variation and also daily range was smaller in other seasons except weaker dailyvariation in summer at Waliguan.But the surface O_3 concentration(SOC)in summer was higherthan that in winter at Waliguan.The SOC on clear days of summer at Waliguan was over 20 ppbhigher than at Longfengshan and Lin'an.The global radiation and NO_x concentration were themain factors which control the SOC on clear days at Longfengshan and Lin'an.and playedimportant role in different seasons and areas.The transportation of air flow around the area ofQinghai-Xizang(Tibet)Plateau was the main cause for high SOC and weak daily variation insummer at Waliguan.The similar effect of transportation was obtained at the Mauna LoaObservatory.The distribution characteristics of SOC increasing with height in the tropospheredetermined the difference of SOC between East China and West China.  相似文献   

4.
中国大气本底条件下不同地区地面臭氧特征   总被引：20，自引：1，他引：20  
分析了晴天和阴天时瓦里关本底台、临安和龙凤山本底站地面 O3浓度的特点。晴天时 ,临安站地面 O3有明显日变化 ,以春季最大 (42 .9× 1 0 - 9) ,夏季最小 (2 0 .3× 1 0 - 9) ;龙凤山站日变化更规则 ,秋季最大 (约 2 7× 1 0 - 9) ;瓦里关本底台除了夏季有微弱日变化外 ,其它季节没有明显的日变化 ,日较差也很小 ,但夏季地面 O3浓度显著高於冬季 ;夏季晴天瓦里关地面O3浓度要比龙凤山、临安高 2 0× 1 0 - 9以上。阴天时 ,临安和龙凤山站除了日变化不很规则和日较差较小外 ,其它大致与晴天相同。阴天时瓦里关不仅没有日变化 ,而且日较差更小 ,但夏季地面 O3仍然高於冬季。太阳总辐射和 NOx 浓度是控制龙凤山和临安晴天和阴天地面O3浓度的决定性因子 ,它在不同季节和地区发挥着重要作用。夏季青藏高原周围地区气流向高原输送作用 ,是形成夏季瓦里关地面 O3高值以及微弱日变化的主要原因。在美国 MaunaLoa基准站也曾观测到类似的输送影响。O3在低对流层随垂直高度增加的分布特征 ,决定了东西部测点地面 O3的差异  相似文献   

5.
Estimates of the Chemical Budget for Ozone at Waliguan Observatory   总被引：6，自引：0，他引：6  
Waliguan Observatory (WO) is an in-land Global Atmosphere Watch (GAW) baseline station on the Tibetan plateau. In addition to the routine GAW measurement program at WO, measurements of trace gases, especially ozone precursors, were made for some periods from 1994 to 1996. The ozone chemical budget at WO was estimated using a box model constrained by these measured trace gas concentrations and meteorological variables. Air masses at WO are usually affected by the boundary layer (BL) in the daytime associated with an upslope flow, while it is affected by the free troposphere (FT) at night associated with a downslope flow. An anti-relationship between ozone and water vapor concentrations at WO is found by investigating the average diurnal cycle pattern of ozone and water vapor under clear sky conditions. This relationship implies that air masses at WO have both the FT and BL characteristics. Model simulations were carried out for clear sky conditions in January and July of 1996, respectively. The chemical characteristics of mixed air masses (MC) and of free tropospheric air masses (FT) at WO were investigated. The effects of the variation in NOx and water vapor concentrations on the chemical budget of ozone at WO were evaluated for the considered periods of time. It was shown that ozone was net produced in January and net destroyed in July for both FT and MC conditions at WO. The estimated net ozone production rate at WO was –0.1 to 0.4 ppbv day–1 in FT air of January, 0.0 to 1.0 ppbv day–1 in MC air of January, –4.9 to –0.2 ppbv day–1 in FT air of July, and –5.1 to 2.1 ppbv day–1 in MC air of July.  相似文献   

6.
A photochemical box model has been used to model themeasured diurnal ozone cycle in spring at Jungfraujochin the Swiss Alps. The comparison of the modelleddiurnal ozone cycle with the mean measured diurnalozone cycle in spring, over the period 1988–1996,shows a good agreement both with regard to the shapeand amplitude. Ozone concentrations increase duringthe daytime and reach a maximum at about 16:00–17:00(GMT) in both the modelled and the mean observed ozonecycle, indicative of net ozone production during thedaytime at Jungfraujoch in spring. The agreement isbetter when the modelled ozone cycle is compared withthe mean measured diurnal cycle (1988–1996) filteredfor north-westerly winds >5 m/s (representative ofregional background conditions at Jungfraujoch). Inaddition to ozone, the modelled diurnal cycle of[HO2] + [CH3O2] also shows rather goodagreement with the mean diurnal cycle of the peroxyradicals measured during FREETEX '96, a FREETropopsheric Experiment at Jungfraujoch in April/May1996. Furthermore, this mean diurnal cycle of the sumof the peroxy radicals measured during FREETEX '96 isused to calculate, using steady-state expressions, therespective diurnal cycle of the OH radical. Thecomparison of the OH diurnal cycle, calculated fromthe peroxy radical measurements during FREETEX '96,with the modelled one, reveals also good agreement.The net ozone production rate during the day-time is0.27 ppbv h-1 from the model, and 0.13 ppbvh-1 from the observations during FREETEX '96. Theobservations and model results both suggest that thediurnal ozone variation in spring at Jungfraujoch isprimarily of photochemical origin. Furthermore, theobserved and modelled positive net ozone productionrates imply that tropospheric in situphotochemistry contributes significantly to theobserved high spring ozone values in the observedbroad spring-summer ozone maximum at Jungfraujoch.  相似文献   

7.
临安秋季近地层非甲烷碳氢化合物特征   总被引：4，自引：1，他引：3  
应用浙江临安1999年秋季非甲烷碳氢化合物(NMHC)观测数据,分析了NMHC特征,并估计其对该地O3的影响.该地NMHC芳香烃含量最高为47.9%,其次为:烷烃29.1%,烯烃12.7%,炔烃8.2%,生物排放的烃2.1%.从各NMHC成份相关分析发现,NMHC主要排放源是该地生物物质(柴草、秸秆、农业废弃物)焚烧,存在未知芳香烃人为源的可能.丙烯等量浓度分析表明,芳香烃、CO、生物源烃和烯烃对该地O3均有重要贡献.观测和模式分析显示本次观测的O3处于NMHC控制区.  相似文献   

8.
Free tropospheric measurements of ozone, peroxyacetylnitrate andprecursors (CO, NMHC) that were made within the framework of the EUROTRACsub-project TOR (Tropospheric Ozone Research) between 1990 and 1995 at theGAW station Izana, Tenerife (28°18N, 16°30W) arediscussed. The average annual cycles reveal the importance of transport fromnorthern mid-latitudes and the role of photo-chemistry. According toair-mass trajectories, which were supplied to us from AEROCE(Atmosphere/Ocean Chemistry Experiment), transport from northernmid-latitudes is associated with high precursor concentrations in winter,whereas ozone concentrations in winter are not much influenced by transportpatterns, suggesting a rather uniform distribution over the northern part ofthe Northern Hemisphere around mean value of 43 ± 5 ppb. In summer,high ozone concentrations of up to 90 ppb are often encountered duringtransport from north, while the levels of precursors are much lower than inwinter, because of photochemical destruction. Trajectories from southerlylatitudes and the Sahara usually have the lowest ozone concentrationsassociated with them.  相似文献   

9.
A one-year set of surface ozone measurements in a four-station network located in the Venezuelan savannah is reported. The diurnal ozone variation is typical of continental stations with a maximum in the afternoon, when vertical turbulent mixing is strongest. The annual O3 average concentration, based on the monthly averages of daily maxima, was 17±2 ppb, which is in good agreement with values reported for similar latitudes. The boundary-layer ozone levels did not fall below 8 ppb, in contrast with previous sporadic measurements made in tropical latitudes. No evidence was found that mesoscale O3 downdrafts in the ITCZ in the South American continent are an important source of surface ozone. Finally, it is suggested that the relatively high ozone levels observed at the end of the dry season are probably of photochemical origin.  相似文献   

10.
Through one and half year continuous in-situ measurements,the distributions and variations of surface ozone and its precursors at a typical mixed agricultural and metropolitan area-Changshu,Yangtze Delta region,were studied.The preliminary analysis on the concentration levels and variations of surface ozone indicated the obvious seasonal and diurnal cycles during the experiment.The hourly averaged concentrations of surface ozone were high,in about 17% of total valid hours the surface ozone concentration exceeded 50 ppb,and in 22 days the hourly averaged ozone concentration was greater than 100 ppb.There were about 40% of the days in that the daily maximum 8-hour ozone concentration was greater than 50 ppb.The days with daily maximum 8-hour ozone concentration greater than 80 ppb were about 33 days that accounted for about 8% of the observational days.The variations of 5-day moving averaged ozone concentrations depended both on the weather conditions and on the changes of ozone in background atmosphere.Photochemical process had the significant impacts on ozone productions.  相似文献   

11.
我国北方地区对流层中下层臭氧收支   总被引：1，自引：0，他引：1       下载免费PDF全文
为了揭示我国北方地区对流层中下层臭氧(O3) 的形成机理以及周边地区的污染输送对我国北方地区对流层中下层O3收支的影响, 在与外场观测数据比较分析的基础上, 利用全球化学输送模式(MOZART-2) 采用收支分析方法定量分析了影响我国北方地区对流层中下层O3的各个物理化学过程。结果表明:我国北方地区对流层下层O3最重要的来源是光化学生成作用, 约占总来源的58.3%(41.5 Tg), 光化学生成反应中HO2对于O3生成的贡献最大; 最大的汇是干沉降过程, 约占总汇的43.2%(26.2Tg); 水平净输送作用对我国北方地区对流层中下层O3收支的影响非常大, 在我国北方地区对流层下层, 41.6%左右的O3来自水平净输送, 随高度增加, 水平输送影响增大, 我国北方地区对流层中层大约81.5%的O3来自水平净输送。  相似文献   

12.
The observational results in Lin'an show the elevated average concentrations of surface ozone and Nitric Oxides(NO_x)in the rural area in the eastern mid-latitudes of China.The mechanism of its variations was explained by the theo-retical analysis.In the case of breeze,the photochemical reactions controlled by solar radiation is the determined factorsaffecting the variations of the surface O_3 and NO_x.A study of the correlation between NO_x and SO_2 demonstrates thatthe biomass burning is an important local emission source of NO_x.  相似文献   

13.
The ozone forming potential of VOCs and NOx for plumes observed from several cities and a power plant in eastern Germany was investigated. A closed box model with a gas phase photochemical reaction mechanism was employed to simulate several scenarios based upon aircraft observations. In several of the scenarios, the initial concentrations of NOx, VOCs, and SO2, were reduced to study the factors limiting the O3 production. Ozone production was limited by the initial VOC concentrations for all of the simulated plumes. Higher O3 concentrations were produced with reduced initial NOx. In one sample with high SO2 mixing ratios (>100 ppb), SO2 was also identified as a significant contributor to the production of O3.  相似文献   

14.
The mixing ratios for ozone and NOx (NO+NO2) have been measured at a rural site in the United States. From the seasonal and diurnal trends in the ozone mixing ratio over a wide range of NOx levels, we have drawn certain conclusions concerning the ozone level expected at this site in the absence of local photochemical production of ozone associated with NOx from anthropogenic sources. In the summer (June 1 to September 1), the daily photochemical production of ozone is found to increase in a linear fashion with increasing NOx mixing ratio. For NOx mixing ratios less than 1 part per billion by volume (ppbv), the daily increase is found to be (17±3) [NOx]. In contrast, the winter data (December 1 to March 1) indicate no significant increase in the afternoon ozone level, suggesting that the photochemical production of ozone during the day in winter approximately balances the chemical titration of ozone by NO and other pollutants in the air. The extrapolated intercept corresponding to [NOx]=0 taken from the summer afternoon data is 13% less than that observed from the summer morning data, suggesting a daytime removal mechanism for O3 in summer that is attributed to the effects of both chemistry and surface deposition. No significant difference is observed in the intercepts inferred from the morning and afternoon data taken during the winter.The results contained herein are used to deduce the background ozone level at the measurement site as a function of season. This background is equated with the natural ozone background during winter. However, the summer data suggest that the background ozone level at our site is elevated relative to expected natural ozone levels during the summer even at low NOx levels. Finally, the monthly daytime ozone mixing ratios are reported for 0[NOx]0.2 ppbv, 0.3 ppbv[NOx]0.7 ppbv and 1 ppbv[NOx]. These monthly ozone averages reflect the seasonal ozone dependence on the NOx level.  相似文献   

15.
The analysis of surface ozone variability requires besides chemicalstudies the consideration of meteorological conditions and dynamicprocesses. Our research focuses on the mechanisms in connection with coldfront passages. A statistical study and case studies of cold front passageswere carried out at six German ground-based sites during the year 1990.After the passage of cold fronts three typical developments of thenear-ground ozone concentrations could be identified. Usually the ozoneconcentrations decrease due to advection of clean air masses or due toenhanced cloudiness preventing the photochemical production of ozone,chemical destruction by nitrogenoxides, and heterogeneous chemistry. In somecases the concentrations increased by reason of downward mixing of ozoneenriched air intruded from the stratosphere into the troposphere bytropopause foldings. For a few cases no modification set in. The decreasewas mostly twice as strong as the increase. The latter was between 4 and 8ppb on the average. Special emphasis is given to the transport ofstratospheric ozone down to the ground. There is no direct evidence forstratospheric ozone at ground level, because it cant be distinguished fromthe tropospheric one, but from case studies circumstantial evidence is foundin favour of it. As an example of increasing ozone behind the passage ofcold fronts one case study typical of all other case studies is presented.It shows the characteristic properties of the corresponding fronts, whichare fast movement, a vertical split structure and strong convection.  相似文献   

16.
Reactive halogen species (RHS = X, XO, HOX, OXO; X = Cl, Br, I) are known to have an important influence on the chemistry in the polar boundary layer (BL), where they are responsible for ozone depletion events in spring. Recent field campaigns at Mace Head, Ireland, and the Dead Sea, Israel, identified for the first time iodine oxide (IO) at mixing ratios of up to 6.6 ppt and 90 ppt bromine oxide (BrO), respectively, by DOAS also at lower latitudes. These results intensified the discussion about the role of the RHS in the mid-latitude BL.Photochemical box model calculations show that the observed IO mixing ratios can destroy ~0.45 ppb ozone per hour. This is comparable to the rates of the known O3-loss processes in the boundary layer. The model studies also reveal that IO, at these levels, has a strong influence on the BL photochemistry, increasing the OH/HO2- and the NO2/NO - ratios. In combination these changes lead to a reduction of the photochemical ozone formation, which - in addition - reduces ozone mixing ratios by up to 0.15 ppb/h.The studies for the Dead Sea case give no information on the heterogeneous process responsible for the bromine release, but they show that a total of 2 – 4 ppb of total bromine have to be released to explain the observed complete depletion of 60 ppb ozone in 2 – 3 hours.  相似文献   

17.
Local ozone production and loss rates for the arctic free troposphere (58–85° N, 1–6 km, February–May) during the TroposphericOzone Production about the Spring Equinox (TOPSE) campaign were calculated using a constrained photochemical box model. Estimates were made to assess the importance of local photochemical ozone production relative to transport in accounting for the springtime maximum in arctic free tropospheric ozone. Ozone production and loss rates from our diel steady-state box model constrained by median observations were first compared to two point box models, one run to instantaneous steady-state and the other run to diel steady-state. A consistent picture of local ozone photochemistry was derived by all three box models suggesting that differences between the approaches were not critical. Our model-derived ozone production rates increased by a factor of 28 in the 1–3 km layer and a factor of 7 in the 3–6 kmlayer between February and May. The arctic ozone budget required net import of ozone into the arctic free troposphere throughout the campaign; however, the transport term exceeded the photochemical production only in the lower free troposphere (1–3 km) between February and March. Gross ozone production rates were calculated to increase linearly with NOx mixing ratiosup to 300 pptv in February and for NOx mixing ratios up to 500 pptv in May. These NOx limits are an order of magnitude higher thanmedian NOx levels observed, illustrating the strong dependence ofgross ozone production rates on NOx mixing ratios for the majority of theobservations. The threshold NOx mixing ratio needed for netpositive ozone production was also calculated to increase from NOx 10pptv in February to 25 pptv in May, suggesting that the NOx levels needed to sustain net ozone production are lower in winter than spring. This lower NOx threshold explains how wintertime photochemical ozone production can impact the build-up of ozone over winter and early spring. There is also an altitude dependence as the threshold NOx neededto produce net ozone shifts to higher values at lower altitudes. This partly explains the calculation of net ozone destruction for the 1–3 km layerand net ozone production for the 3–6 km layer throughout the campaign.  相似文献   

18.
Analysis of tropospheric ozone residual (TOR) data from satellite measurements indicates an increasing trend of tropospheric ozone over the Yangtze Delta region of China. The increasing trend can be derived both from the annual mean TOR and from the monthly mean TOR except for January and March. The increase rate of the decadal mean TOR was 0.82 DU during 1978-2000. The impact of this long-term trend on the climate and atmospheric oxidizing capacity over the region should be further studied. Data comparison shows a significant correlation between the TOR and surface ozone data collected at Lin'an background station in the Yangtze Delta region, suggesting an internal connection between both quantities.  相似文献   

19.
A photochemical box model has been used to simulate the mixing ratio ofozone under conditions reflecting those encountered in the marine boundarylayer at Cape Grim, Tasmania, where a decade-long record of ozone mixingratio is available. The model is based on the proposition that ozone loss byphotolysis, atmospheric reaction with hydroperoxy and hydroxyl radicals, andsurface deposition is balanced by ozone gain via entrainment from the lowerfree troposphere with a small additional source in summer from photolysis ofnitrogen dioxide. This model simulates very well the observed ozone records,reproducing both the small diurnal cycle in ozone mixing ratio observedduring the summer months, and the factor of two seasonal ozone cycle showinga distinct winter maximum and summer minimum. The model result confirms thatunder the low-NOx conditions of the clean marine boundarylayer net photochemical loss of ozone occurs at all times of year.  相似文献   

20.
临安地区地面SO2变化规律及其源地分析   总被引：5，自引：1，他引：4  
利用后向轨迹的簇分析方法,研究了1994年9、10月份不同流场条件时,临安地面SO2的变化规律。采用Lagrangian传输、扩散、沉降模式计算了中国大陆以及东部较发达的几个区域对临安地面SO2的贡献。与实际观测资料对比表明,模式能够较好地模拟出临安地面SO2的浓度量级和变化趋势。同时,模式结果也表明,作为区域污染背景监测站,临安站观测的SO2浓度大小及变化趋势能反映中国东部发达地区SO2的浓度水平。  相似文献   

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