共查询到20条相似文献，搜索用时 544 毫秒
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近地面O3变化化学反应机理的数值研究 总被引：34，自引：1，他引：33
利用中尺度气象模式（MM5）及区域化学模式（RADM）对中国地区近地面O3变化化学反应机理进行了数值模拟研究。主要研究了近地面O3变化与其主要前体物NMHC（非甲烷烃）、NOx、CO等之间复杂相互作用关系。主要结论为:（1） 污染地区近地面O3变化主要受光化学作用控制;而清洁地区地面O3变化主要受大气背景O3浓度影响。（2）NMHC和NOx的变化对HO2和OH自由基的影响是十分复杂的,O3的反馈作用对自由基的影响是不可忽视的。（3）在高NOx污染地区的地面上空可能出现高O3污染。（4）在O3光化学反应机理中同样存在线性相关关系。 相似文献
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1992年大气甲烷增长速率异常
下降的模拟研究 总被引：4，自引：0，他引：4
应用初步建立的全球二维大气化学模式,模拟了甲烷、一氧化碳和OH自由基自工业革命以来的长期变化,对1992年大气中甲烷增长速率突然下降这一异常现象的可能原因如平流层O3下降,皮纳图博火山引起对流层温度下降、甲烷排放源减少等逐一进行了定量研究。研究还发现一氧化碳排放源的减少是另一重要影响因子,并进行了验证。结果表明,1992年甲烷增长速率急剧下降的主要原因来自甲烷和一氧化碳排放源的减少。 相似文献
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华南区域大气成分业务数值预报GRACEs模式系统 总被引：1，自引：0，他引：1
总结了华南区域大气成分数值预报GRACEs模式系统的业务发展进程,系统介绍了GRACEs模式的计算域、气象驱动场、输入排放源、计算平台与产品应用,报告了GRACEs模式的业务预报性能。概述了国内外大气成分数值预报模式的发展现状与趋势,介绍了新版CMAQ模式Ver5.1的化学机理,及其在光化学、气溶胶化学、源排放、化学与气象双向反馈机制等方面的重要更新。GRACEs模式系统预期将在本地精细化气象模式、污染源本地化、化学机理以及初始场同化等方面进一步研究,深入开展华南区域"一体化"大气成分模式系统的研发与应用。 相似文献
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应用查表法模拟区域对流层O3、Nox分布和演化的研究 总被引：2，自引：0，他引：2
应用STEM-II气相光化学模式探讨了影响对流层O3、NOx气相光化学转化率的各物理、化学因子。表明在我国多数地区光化学污染物特征(NMHC/NOx较高)下,光辐射强度、温度、初始O3浓度和NOx浓度是影响O3、NOx气相光化学转化率的主要因子。将以上因子分档组合,计算并建立了各种情况下O3、NOx气相光化学转化率的查算表,并将之用于模拟区域O3、NOx的演化和分布。结果表明,与光化学模式直接耦合计算法相比,该方法既能显著缩短计算时间,又能基本反映大气化学反应的非线性过程,并与直接耦合法符合得较好。 相似文献
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应用查表法模拟区域对流层O3、Nox分布和演化的研究 总被引：1，自引：0，他引：1
应用STEM-II气相光化学模式探讨了影响对流层O3、NOx气相光化学转化率的各物理、化学因子。表明在我国多数地区光化学污染物特征(NMHC/NOx较高)下，光辐射强度、温度、初始O3浓度和NOx浓度是影响O3、NOx气相光化学转化率的主要因子。将以上因子分档组合，计算并建立了各种情况下O3、NOx气相光化学转化率的查算表，并将之用于模拟区域O3、NOx的演化和分布。结果表明，与光化学模式直接耦合计算法相比，该方法既能显著缩短计算时间，又能基本反映大气化学反应的非线性过程，并与直接耦合法符合得较好。 相似文献
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利用中尺度大气化学模式WRF/Chem对2013年3月6日华南地区一次平流层入侵事件及其对对流层低层臭氧的影响进行模拟研究。通过加入UBC（Upper Boundary Condition）上边界处理方案,弥补WRF/Chem模式未考虑平流层臭氧化学反应的不足。结合臭氧探空廓线资料、地面O3、CO、NOx、相对湿度、温度和风速等观测资料以及再分析资料对模拟结果进行定量评估,结果表明模式能较为真实地模拟本次平流层入侵过程。模拟分析进一步揭示:（1）副热带高空急流是本次平流层入侵的主要原因。当华南地区处在副热带急流入口区左侧下沉区域时,平流层入侵将富含臭氧的干燥空气输送到对流层中低层。（2）本次平流层入侵对对流层低层臭氧收支有重要影响,导致香港地区近地层臭氧体积混合比浓度明显上升,如塔门站夜间臭氧浓度升高21.3 ppb（1 ppb=1×10-9）。地面气象场和化学物种的分析进一步确认了平流层入侵的贡献。（3）采用动力学对流层顶高度时零维箱式模型和Wei公式计算得到的平流层入侵通量相当,分别为-1.42×10-3 kg m-2 s-1和-1.59×10-3 kg m-2 s-1,这一结果与前人研究相吻合,且与采用热力学对流层顶高度计算所得到的结果具有可比性。 相似文献
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By means of a three-dimensional meteorological model (MM5) and a chemical model,the distributions of tropospheric ozone and its precursors over China have been simulated in summer and winter time,16-18 August 1994 and 7-9 January 1995.The distribution of ozone over the Tibetan Plateau in summer time is deeply discussed.The simulated results indicate that thedistributions of surface ozone and NOx are in good agreement with observed results,and human activities and photochemical reactions are the main factors controlling the surface ozone and NOx concentrations.In addition,higher ozone concentrations are coincided with the air convergence,and the lower concentrations are related to the air divergence.In summer,over the Tibetan Plateau the strong flow convergence results in higher ozone concentrations in the lower troposphere:and the strong flow divergence results in lower ozone concentrations in the upper troposphere.In winter time ozone concentrations show large-scale characteristics controlled by westerly flow,and in the jet area they are lower than those outside the jet. 相似文献
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我国对流层大气臭氧的数值模拟 总被引：7，自引：2，他引：7
本文建立了一个用于对流层大气臭氧模拟的三维欧拉模式,针对影响臭氧光化学转化的各种因素及我国城市光化学污染的特点,模式中简化了光化学项的计算。根据实际观测资料,提出了模拟云雾对臭氧影响的参数化方法,并确定了云雾作用系数,通过模式的数值模拟,得出了我国对流层大气臭氧,特别是近地面层大气臭氧的分布状况、我国城市光化学污染的分布特征以及它们的季节变化规律. 相似文献
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The relationship between the emission of ozone precursors and the chemical production of tropospheric ozone(O3) in the Pearl River Delta Region(PRD) was studied using numerical simulation.The aim of this study was to examine the volatile organic compound(VOC)-or nitrogen oxide(NOx =NO+NO2)limited conditions at present and when surface temperature is increasing due to global warming,thus to make recommendations for future ozone abatement policies for the PRD region.The model used for this application is the U.S.Environmental Protection Agency’s(EPA’s) third-generation air-quality modeling system;it consists of the mesoscale meteorological model MM5 and the chemical transport model named Community Multi-scale Air Quality(CMAQ).A series of sensitivity tests were conducted to assess the influence of VOC and NOx variations on ozone production.Tropical cyclone was shown to be one of the important synoptic weather patterns leading to ozone pollution.The simulations were based on a tropicalcyclone-related episode that occurred during 14-16 September 2004.The results show that,in the future,the control strategy for emissions should be tightened.To reduce the current level of ozone to meet the Hong Kong Environmental Protection Department(EPD) air-quality objective(hourly average of 120 ppb),emphasis should be put on restricting the increase of NOx emissions.Furthermore,for a wide range of possible changes in precursor emissions,temperature increase will increase the ozone peak in the PRD region;the areas affected by photochemical smog are growing wider,but the locations of the ozone plume are rather invariant. 相似文献
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A chemical module describing the tropospheric photochemistry of ozone precursors in both gaseous and aqueous phases for a remote continental atmosphere has been developed within the framework of a two-dimensional cloud model. Dynamical, microphysical and chemical processes are fully interacting in order to study the influence of clouds on ozone chemistry and to quantify the relative importance of the different processes on the budget and evolution of 12 chemical species. Whereas the concentrations of highly soluble species are strongly affected by evaporation and sedimentation, less soluble species are affected primarily by accretion. The model reproduces previously observed chemical phenomena such as the enrichment of formic acid at the top of the cloud. 相似文献
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Fast-J: Accurate Simulation of In- and Below-Cloud Photolysis in Tropospheric Chemical Models 总被引：3，自引：0，他引：3
Photolysis rates in the troposphere are greatly affected by the presenceof cloud and aerosol layers. Yet, the spatial variability of theselayers along with the difficulty of multiple-scattering calculationsfor large particles makes their inclusion in 3-D chemical transportmodels computationally very expensive.This study presents a flexible and accurate photolysis scheme, Fast-J,which calculates photolysis rates in the presence of an arbitrary mix ofcloud and aerosol layers. The algorithm is sufficiently fast to allow thescheme to be incorporated into 3-D global chemical transport models andhave photolysis rates updated hourly. It enables tropospheric chemistrysimulations to include directly the physical properties of the scatteringand absorbing particles in the column, including the full, untruncatedscattering phase function and the total, uncorrected optical depth.The Fast-J scheme is compared with earlier methods that have been usedin 3-D models to parameterize the effects of clouds on photolysis rates.The impact of Fast-J on tropospheric ozone chemistry is demonstratedwith the UCI tropospheric CTM. 相似文献
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通过WACCM-3模式中气溶胶光学厚度与卫星资料的对比发现,模式可以很好地再现全球气溶胶的主要分布特征,但在一些区域还存在数值上的差异。利用数值试验研究对流层气溶胶的直接气候效应对平流层气候的影响,结果表明:对流层气溶胶对平流层气候有明显影响,平流层化学过程在这一影响中起重要作用,而对流层气溶胶对平流层辐射的影响不是其直接气候效应对平流层影响的主要原因。其机制可能是对流层气溶胶改变对流层的辐射平衡,影响对流层的温度和大气环流,进而影响行星波的上传,使得平流层气候发生变化;影响区域主要位于高纬度和极地地区,南半球的变化比北半球大,温度变化最大达10 K,纬向风变化最大可达12 m/s,臭氧体积分数最多减少0.8×10-6。 相似文献
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The global three-dimensional Lagrangian chemistry-transport model STOCHEM has been used to follow the changes in the tropospheric distributions of the two major radiatively-active trace gases, methane and tropospheric ozone, following the emission of pulses of the short-lived tropospheric ozone precursor species, methane, carbon monoxide, NOx and hydrogen. The radiative impacts of NOx emissionswere dependent on the location chosen for the emission pulse, whether at the surface or in the upper troposphere or whether in the northern or southern hemispheres. Global warming potentials were derived for each of the short-lived tropospheric ozone precursor species by integrating the methane and tropospheric ozone responses over a 100 year time horizon. Indirect radiative forcing due to methane and tropospheric ozone changes appear to be significant for all of the tropospheric ozone precursor species studied. Whereas the radiative forcing from methane changes is likely to be dominated by methane emissions, that from tropospheric ozone changes is controlled by all the tropospheric ozone precursor gases, particularly NOxemissions. The indirect radiative forcing impacts of tropospheric ozone changes may be large enough such that ozone precursors should be considered in the basket of trace gases through which policy-makers aim to combat global climate change. 相似文献
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利用臭氧探空资料,分析了西太平洋地区香港(Hong Kong)、那霸(Naha)和札幌(Sapporo)三个站点2000~2010年期间大气边界层内臭氧(O3)的季节分布和年变化趋势。结果表明,三个站点O3的季节分布存在明显的差异。其中,那霸和香港大气边界层内O3季节平均呈双峰值分布,其峰值分别出现在春季和秋季;而札幌站为单峰分布,峰值出现在春季。造成季节分布差异的主要原因包括人为污染源和自然因素如气象条件。另外,三个站点大气边界层内O3均呈上升趋势。其中札幌、那霸上升最快,分别达0.80 ppb a-1和0.77 ppb a-1。(ppb表示10-9,下同)香港的年际增长较不明显,但秋季增长却非常明显,高达1.21 ppb a-1。结合GOME (Global Ozone Monitoring Experiment) 和SCIAMACHY (Scanning Imaging Absorption Spectro Meter for Atmospheric Chartography)卫星反演的NO2数据发现,过去10年中国京津唐和东北地区的对流层内NO2柱总量增加极为迅速。这些O3前体物通过远距离输送是导致札幌、那霸O3浓度增加的主要原因之一。珠江三角洲人为污染源的增加及偏北气流的影响,是导致香港地区秋季O3增加的主要原因。 相似文献
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北京奥运会期间CBM-Z化学机制的模拟应用 总被引：1，自引：0，他引：1
利用CBM-Z化学机制模拟了中国科学院大气物理研究所气象塔站在北京奥运会期间高臭氧时段O3浓度的日变化,评估了气象条件、北京奥运会加强控制措施以及O3前体物浓度对近地面O3生成的影响。结果表明:(1)CBM-Z化学机制较好地模拟了北京奥运会期间典型时段气象塔站O3、NO、NO2日变化特征。(2)有利于局地高臭氧事件发生的气象条件非常相似;北京奥运会加强控制措施的实施显著减少了NOx及VOCs的排放量,导致近地面O3浓度的明显下降。(3)奥运会期间VOCs和CO是影响气象塔站O3生成量的关键因素。 相似文献
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This study estimated the largely unstudied downward transport and modification of tropospheric ozone associated with tropical
moist convection using a coupled meteorology-chemistry model. High-resolution cloud resolving model simulations were conducted
for deep moist convection events over West Africa during August 2006 to estimate vertical transport of ozone due to convection.
Model simulations realistically reproduced the characteristics of deep convection as revealed by the estimated spatial distribution
of temperature, moisture, cloud reflectivity, and vertical profiles of temperature and moisture. Also, results indicated that
vertical transport reduced ozone by 50% (50 parts per billion by volume, ppbv) in the upper atmosphere (12–15 km) and enhanced
ozone by 39% (10 ppbv) in the lower atmosphere (<2 km). Field observations confirmed model results and indicated that surface
ozone levels abruptly increased by 10–30 ppbv in the area impacted by convection due to transport by downdrafts from the upper
troposphere. Once in the lower troposphere, the lifetime of ozone decreased due to enhanced dry deposition and chemical sinks.
Ozone removal via dry deposition increased by 100% compared to non-convective conditions. The redistribution of tropospheric
ozone substantially changed hydroxyl radical formation in the continental tropical boundary layer. Therefore, an important
conclusion of this study is that the redistribution of tropospheric ozone, due to deep convection in non-polluted tropical
regions, can simultaneously reduce the atmospheric loading of ozone and substantially impact the oxidation capacity of the
lower atmosphere via the enhanced formation of hydroxyl radicals. 相似文献