Interannual and Decadal Changes in Tropospheric Ozone in China and the Associated Chemistry–Climate Interactions: A Review

China has been experiencing widespread air pollution due to rapid industrialization and urbanization in recent decades.The two major concerns of ambient air quality in China are particulate matter(PM) and tropospheric ozone(O_3). With the implementation of air pollution prevention and control actions in the last five years, the PM pollution in China has been substantially reduced. In contrast, under the conditions of the urban air pollution complex, the elevated O_3 levels in city clusters of eastern China, especially in warm seasons, have drawn increasing attention. Emissions of air pollutants and their precursors not only contribute to regional air quality, but also alter climate. Climate change in turn can change chemical processes, long-range transport, and local meteorology that influence air pollution. Compared to PM, less is known about O_3 pollution and its climate effects over China. Here, we present a review of the main findings from the literature over the period 2011–18 with regard to the characteristics of O_3 concentrations in China and the mechanisms that drive its interannual to decadal variations, aiming to identify robust conclusions that may guide decision-making for emissions control and to highlight critical knowledge gaps. We also review regional and global modeling studies that have investigated the impacts of tropospheric O_3 on climate, as well as the projections of future tropospheric O_3 owing to climate and/or emission changes.     

2015-2019年贵港市臭氧污染特征及其与气象要素的关系

为研究贵港市O3(臭氧)污染特征及其与气象要素的关系,对2015-2019年贵港市国家空气自动监测站和同期贵港国家气象观测站逐日、逐时气象资料进行了研究和分析.结果表明:近5a来贵港市O3污染日趋严重;O3污染存在明显的季节变化,秋＞夏＞春＞冬;O3浓度日变化特征呈单峰型,8:00出现谷值,15:00-16:00出现峰...     

利用臭氧氧化发光光谱特征检测水质污染

利用不同的污染物质在被臭氧氧化时发光特性不同的原理检测水质污染。检测出来的发光光谱与不同污染源的特征光谱进行对比,辅助发光时序等特征,检测几种污染物的含量和确定污染源。对涉及的有关技术问题进行了探讨。     

On the nonlinear response of lower stratospheric ozone to NOx and ClOx perturbations for different CH4 sources

The impact of sulfate aerosol, ClOx and NOx perturbations for two different magnitudes of CH4 sources on lower stratospheric ozone is studied by using a heterogeneous chemical system that consists of 19 species belonging to 5 chemical families （oxygen, hydrogen, nitrogen, chlorine and carbon）. The results show that the present modeled photochemical system can present several different solutions, for instance, periodic states and multi-equilibrium states appearing in turn under certain parameter domains, through chlorine chemistry and nitrogen chemistry together with sulfate aerosol as well as the increasing magnitude of CH4 sources. The existence of catastrophic transitions could produce a dramatic reduction in the ozone concentration with the increase of external sources.     

云顶以下臭氧对TOMS反演臭氧总量的影响及反演方法的理论研究

目前紫外后向散射反演臭氧总量的所有算法,都将云考虑成不透明的Lambertian反射体,并假定云顶有效反照率不随波长的变化而变化.然而本文通过模拟计算发现,由于云散射、瑞利散射、臭氧吸收三种作用的综合结果,云顶的有效反照率是与波长相关的,即使光学厚度比较大的云,辐射也可由云顶继续向下传输,因而会受到云顶以下臭氧吸收的影响.用V7方法进行反演,模拟计算结果表明：云的出现使得云顶以下,特别是云内光程增强,导致紫外波段的臭氧吸收衰减增大,所以反演出的臭氧总量值比真实值偏大,本文称这种现象为“云吸收效应”,并讨论了该效应的影响因子.最后,在辐射传输模拟的基础上建立一套反演算法,大大减弱了“云吸收效应”的影响.     

河北沧州市臭氧质量浓度与气象因子的关系分析

利用2014—2020年河北沧州逐小时气象与环境监测数据,对沧州市臭氧(O₃)污染加剧现状及其与气象因子的关系进行分析。结果表明：(1)沧州地区O₃污染呈加剧态势,且O₃已上升为该地区首要污染物;O₃污染集中出现在5—9月,O₃质量浓度日变化呈单峰单谷型,最大浓度出现在16:00前后;(2)5—9月O₃日最大8 h平均质量浓度(简称“O₃-8 h”)所处时段,平均气温、最高气温、相对湿度、总辐射辐照度与O₃质量浓度的相关性较好,本站气压、水汽压和平均风速与O₃质量浓度的相关性未通过显著性检验;(3)5—9月O₃-8 h时段,当同时满足8 h平均气温高于30.9℃、最高气温高于32.7℃、平均相对湿度低于42.1%、平均总辐射辐照度高于505.8 W·m^-2时,出现O₃污染的概率达84%;(4)气象因子不是O₃     

Responses of the tropospheric ozone and odd hydrogen radicals to column ozone change

The response of tropospheric ozone to a change in solar UV penetration due to perturbation on column ozone depends critically on the tropospheric NO _x (NO+NO₂) concentration. At high NO _x or a polluted area where there is net ozone production, a decrease in column ozone will increase the solar UV penetration to the troposphere and thus increase the tropospheric ozone concentration. However, the opposite will occur, for example, at a remote oceanic area where NO _x is so low that there is net ozone destruction. This finding may have important implication on the interpretation of the long term trend of tropospheric ozone. A change in column ozone will also induce change in tropospheric OH, HO₂, and H₂O₂ concentrations which are major oxidants in the troposphere. Thus, the oxidation capacity and, in turn, the abundances of many reduced gases will be perturbed. Our model calculations show that the change in OH, HO₂, and H₂O₂ concentrations are essentially independent of the NO _x concentration.     

Toward an improved global network for determination of tropospheric ozone climatology and trends

An examination of typical tropospheric ozone variability on daily, monthly, annual and interannual timescales and instrumental precision indicates that the current ozonesonde network is insufficient to detect a trend in tropospheric ozone of 1% per year at the 2 level even at stations with records a decade in length. From a trend prediction analysis we conclude that in order to detect a 1% per year trend in a decade or less it will be necessary to decrease the time between observations from its present value of 3–7 days to 1 day or less. The spatial distribution of the current ozonesonde stations is also inadequate for determining the global climatology of ozone. We present a quantitative theory taking into account photochemistry, surface deposition, and wind climatology to define the effectively sampled region for an observing station which, used in conjunction with the instrumental precision and the above prediction analysis, forms the basis for defining a suitable global network for determining regional and global ozone climatology and trends. At least a doubling of the present number of stations is necessary, and the oceans, most of Asia, Africa, and South America are areas where more stations are most needed. Differential absorption lidar ozone instruments have the potential for far more frequent measurements of ozone vertical profiles and hence potentially more accurate climatology and trend determinations than feasible with ozonesondes but may produce a (fair weather) biased data set above the cloud base. A strategy for cloudy regions in which either each station utilizes both lidars and sondes or each station is in fact a doublet comprised of a near-sea-level lidar and a proximal-mountain-top lidar could serve to minimize this bias.     

Nonlinear chemical couplings in the tropospheric NO x -HO x gas phase chemistry

A bifurcation phenomenon with relevance to atmospheric chemistry is discussed. The gasphase reactions in the troposphere exhibit two types of temporal evolution which are controlled by the strength of the source,Q, of nitric oxide, NO, via the nonlinear chemical coupling between the hydrogen oxides and nitrogen oxides chemistry. IfQ remains below a threshold value, all short-lived species, including NO, approach steady-state concentrations, while above the threshold bifurcation to another state with increasing (nonstationary) NO concentrations accompanied by a depletion of the OH and HO₂ abundances takes place.     

北京地区臭氧垂直分布的演变趋势与特征的研究——卫星SBUV资料与地面遥感对比分析

利用地面遥感O₃垂直分布的逆转方法〈C〉测量出的北京上空O₃剖面资料,对雨云7号卫星的SBUV系统测量的同地区的O₃垂直分布数据进行了订正.对订正后的长达8年（1979-1986年）的完整的SBUV资料进行了较为仔细的分析,得出了这一时期内的O₃垂直分布长期演变呈下降趋势.并在上层O₃含量的季节变化特征和周期振荡等方面,有新的发现,得出一些有意义的结果.