Annual and semiannual oscillations of stratospheric ozone

The global structures of annual oscillation (AO) and semiannual oscillation (SAO) of stratospheric ozone are examined by applying spherical harmonic analysis to the ozone data obtained from the Nimbus-7 solar backscattered UV-radiation (SBUV) measurements for the period November 1978 to October 1980. Significant features of the results are: (1) while the stratospheric ozone AO is prevalent only in the polar regions, the ozone SAO prevails both in the equatorial and polar stratospheres; (2) the vertical distribution of the equatorial ozone SAO has a broad maximum of the order of 0.5 (mixing ratio in g/g) and the maximum appears earlier at high altitude (shifting from May [and November] at 0.3 mb [60 km] to November [and May] at 40 mb); (3) above the 40 km level, the maximum of the polar ozone SAO shifts upward towards later phase with altitude with a rate of approximately 10 km/month in both hemispheres; (4) vertical distributions of the polar ozone AOs and SAOs show two peaks in amplitude with a minimum (nodal layer) in between and a rapid phase change with altitude takes place in the respective nodal layers; and (5) the heights of the ozone AO- and SAO-peaks decrease with latitude. The main part of AOs and SAOs of stratospheric ozone including hemispheric asymmetries is ascribable to: (i) temperature dependent ozone photochemistry in the upper stratosphere and mesosphere, (ii) variations of radiation field in the lower stratosphere affected by the annual cycle of solar illumination and temperature in the upper stratosphere and (iii) meridional ozone transport by dynamical processes in the lower stratosphere.     

Systems modelling of stratospheric ozone transport and photochemistry

A scheme of a system of physical and chemical processes controlling the production, transport and destruction of ozone and its gaseous catalysts, as well as other related gases in the low and high stratosphere is presented. An account is made of temperature variations of the stratospheric layer resulting from changes in ozone content; also included is the effect of temperature variations on photochemical reaction rates and ozone and other gases transport between atmospheric layers. Parameters describing major relations of the system are inferred from the analysis of ozone and trace gas data and from the results of model calculations of interdependence between variations in temperature and ozone content of the layer.An analysis of minor fluctuations of the linearized system shows that photochemical processes are responsible for its aperiodic stability and that gas transport between atmospheric layers destabilizes the system.     

Statistical characteristics of the vertical ozone distribution in mid-latitudes

Summary The correlation matrix for the vertical ozone distribution and the temperature-ozone cross-correlation matrix, which was calculated from ozone soundings made over Berlin between 1967 and 1970, the statistical structure of the vertical ozone profile (correlation coefficients, average profiles, average standard deviation, relative variability) was derived for the three ozone seasons. The partial ozone pressure does not at all heights follow a normal distribution (e. g. at tropopause level). Generally, the correlation between tropospheric and stratospheric ozone is rather poor. In some layers the highest correlation coefficients, i.e. –0.3 and +0.4, occur in autumn (October to December) and in winter and spring (January to April). The correlation between the ozone amounts of various stratospheric layers is distinct in autumn, less distinct in summer (May to September) and entirely missing from January to April. Conspicuous cross-correlations between temperature and ozone have been found for all three seasons. a) With a negative correlation between tropospheric temperature and middle tropospheric to middle stratospheric ozone (maximum up to –0.8); b) with a rather strong positive correlation between the ozone amount and the temperature in the lower stratosphere (maximum up to +0.84); c) with a positive correlation between the ozone amount of the middle stratosphere and the temperature of the middle stratosphere (maximum up to +0.8). The highest correlation coefficients occur in autumn.     

Six years of regular ozone soundings over Switzerland

Summary The mean vertical ozone distribution as a function of season is computed from almost 6 years of regular soundings (three times per week) over Switzerland. By comparing the concurrent mean values of the total amount with the 35-year average at Arosa, and by using the correlation between ozone concentration at different levels with the total amount, adjusted values for the seasonal variation of the vertical ozone distribution are obtained which are thought to give a better representation of the long-term climatological mean. The data show a prominent biennial variation of the ozone content around the level of the maximum concentration which does not, however, show up in the total amount because it is missing in the lower stratosphere.     

Application of general circulation models to the study of stratospheric ozone

Summary Observations of the ozone distribution indicate that modifications are required to the photochemical theory. These modifications involve ozone destruction by hydrogen and nitrogen products and ozone transport (both vertical and horizontal) due to atmospheric motions in the stratosphere. If the photochemical terms in the ozone continuity equation are omitted, changes due to atmospheric transport alone can be evaluated.Numerical computations were made of the three-dimensional wind structure as derived from the 12-layer (0–36 km) General Circulation Model developed by NCAR. The results showed that ozone is transported from the equatorial stratosphere poleward and downward in both hemispheres. The horizontal transport is primarily by the Hadley Cell in the tropics and by large-scale eddies in mid and high latitudes. The dominant mechanism for ozone transport are found to be similar to those derived for the horizontal heat and momentum transport found in other general circulation studies.     

Studies of variations in the vertical ozone profiles over India

The latitudinal and temporal variations in the vertical profiles of ozone over the Indian subcontinent are discussed. In the equatorial atmosphere represented by Trivandrum (8°N) and Poona (18°N), while tropospheric ozone shows marked seasonal variations, the basic pattern of the vertical distribution of ozone in the stratosphere remains practically unchanged throughout the year, with a maximum at about 28 to 26 km and a minimum just below the tropopause. The maximum total ozone occurs over Trivandrum in the summer monsoon season and the latitudinal anomaly observed over the Indian monsoon area at this time is explained as arising from the horizontal transport of ozone-rich stratospheric air from over the thermal equator to the southern regions.In the higher latitudes represented by New Delhi (28°N), the maximum occurs at 23 km. Delhi, which lies in the temperate regime in winter, shows marked day-to-day variations in association with western disturbances and the strong westerly jet stream that lies over north and central India at this time.Although the basic pattern of the vertical distribution of ozone in the equatorial atmosphere is generally the same in all seasons, significant though small changes occur in the lower stratosphere and in the troposphere. There are small perturbations in the ozone and temperature structures, distinct ozone maxima being always associated with temperature inversions. There are also large perturbances not related to temperature, ozone-depleted regions normally reflecting a stratification of either destructive processes or materials such as dust layers or clouds at these levels. Particularly interesting are the upper tropospheric levels just below the tropopause where the ozone concentration is consistently the smallest, in all seasons and at all places where soundings have been made in India.     

The summer maximum in total ozone over northwest Europe

Station records of ozone observations have been critically reviewed to investigate the reality of the reported maximum in total ozone over northwest Europe in July. The existence of a longitudinal excess of ozone over the British Isles is confirmed but strong horizontal gradients can be verified only over central Europe and there is no evidence for east-west gradients over the Atlantic. Ozone sounding data as well as total ozone daily variability make it most plausible that the ozone excess over northwest Europe is confined to the lower stratosphere. The isopleths in the region of strong ozone gradients are parallel to the mean flow at 100 mb as required by the calculated constraint on the magnitude of the mean flow advection. It is proposed that analyses of the ozone distribution over oceanic areas could be improved by extending ozone isopleths parallel to the mean lower stratospheric flow from land areas where the pattern is better defined.     

Influence of the vertical motion field on ozone concentration in the stratosphere

Computations of the mean meridional motion field in the stratosphere are applied to ozone distributions to evaluate the associated ozone concentration changes. These changes are compared with those produced by photochemical and quasi-horizontal eddy processes. For the period January–April 1964 there is a cooperative action between the mean and eddy motions with mean subsidence in middle latitudes supplying ozone to be carried polawards and equatorwards by quasi-horizontal eddy processes. At low latitudes mean horizontal motions offset the eddy transport while at high latitudes mean rising motion is the offsetting term. The mean ozone flux through 50 mb, 3.5×10²⁹ molecules sec^–1, is comparable with the fluxes evaluated by other techniques.The spring maximum is thought to be due to a modulation of the energy supply to the stratospheric eddies which, in turn, force the mean motions. Longer-term changes are to be expected; for example during Ice Ages when increased tropospheric eddy activity is anticipated there should be higher total ozone.     

Low ozone event at Madrid in November 1996

A sudden transient increase of the solar ultraviolet (UV) radiation was detected with a ground-based photometer in Madrid (Spain, 41°N, 3°W) on 25 November 1996 (Cordoba et al., 2000. UV-B irradiance at Madrid during 1996, 1997 and 1998. J. Geophys. Res. 105 (D4) (2000) 4903–4906). The data obtained by the TOMS satellite instrument revealed that this event was related to a reduction of the total ozone column values. This low ozone episode has been analysed. The ozone decrease was accompanied by a reduction of air temperature in the lower stratosphere. The anti-correlation between total ozone and air parcel height along the three-dimensional isentropic back-trajectories suggests that the adiabatic uplift of air contributed significantly to both the ozone and the temperature decreases observed. The uplift could be caused by the propagation into the lower stratosphere of the high-pressure cell located over the mid-Atlantic region.     

Estimate of the effect of the 11-year solar activity cycle on the ozone content in the stratosphere

Using spectral, cross-spectral, and regression methods, we analyzed the effect of the 11-year cycle of solar activity on the ozone content in the stratosphere and lower mesosphere via satellite measurement data obtained with the help of SBUV/SBUV2 instruments in 1978–2003. We revealed a high coherence between the ozone content and solar activity level on the solar cycle scale. In much of this area, the ozone content varies approximately in phase with the solar cycle; however, in areas of significant gradients of ozone mixing ratio in the middle stratosphere, the phase shift between ozone and solar oscillations can be considerable, up to π/2. This can be caused by dynamical processes. The altitude maxima of ozone sensitivity to the 11-year solar cycle were found in the upper vicinity of the stratopause (50–55 km), in the middle stratosphere (35–40 km), and the lower stratosphere (below 25 km). Maximal changes in ozone content in the solar cycle (up to 10% and more) were found in winter and spring in polar regions.     

Performance of the electrochemical ozone sonde OSR

Summary The accuracy of the electrochemical ozone sonde, type OSR, has been estimated by analysing tandem ozone soundings of the balloon-borne electrochemical ozone sonde OSR at the Lindenberg Observatory from May to November 1982. A negative bias, though not significant, has been observed above about 28 km for soundings having high single correction factors. Random errors are at their minimum just above the level of the maximum of ozone partial pressure, and reach their maximum in the troposphere. Except at heights above about 28 km the random error of ozone sondes is a factor 2 to 3 times less than the error of the short Umkehr method. Provided that soundings with too high correction factors are neglected, the ozone sonde OSR has an accuracy comparable to that of other Brewer type sondes.The maximum amount of information on the vertical ozone distribution can be drawn from sonde measurements in the lower stratosphere. A study is underway to improve the sensitivity of the sonde OSR and thus to further enhance its reliability.     

Evidence for vertical ozone redistribution since 1967

Long-term measurements of the ozone concentration in the vicinity of the city of Berlin have been performed with ground based Dobson spectrophotometers and balloon borne systems. The respective experiments cover the past 24 years. All data have been reevaluated and corrected towards uniform calibration standards, leading to the longest European data set of total column density, altitude-dependent ozone partial pressures and the corresponding temperatures. Smoothing algorithms unravel significant long-term trends.The analysis shows an increase of ozone concentration within the middle stratosphere (below 31 km height) as well as in the troposphere over the past 24 years. On the contrary, ongoing ozone depletion in the lower stratosphere has been found.The large scale vertical redistribution of atmospheric ozone in the troposphere and the lower stratosphere seems to be in agreement with model calculations and trend predictions that have their roots in changes of the chemical composition and the ozone photochemistry due to anthropogenically induced trace gas concentrations.Deutscher Wetterdienst, Meteorologisches Observatorium Potsdam.Deutscher Wetterdienst, Meteorologisches Observatorium Lindenberg.     

Temperature and ozone variations in the stratosphere

Examined are temperature and ozone variations in the Northern Hemisphere stratosphere during the period 1958–77, as estimated from radiosondes rocketsondes, ozonesondes, and Umkehr measurements. The temperature variation in the low tropical stratosphere is a combination of the variation associated with the quasi-biennial oscillation, and a variation nearly out of phase with the pronounced 3-yearly temperature oscillation (Southern Oscillation) present in the tropical troposphere since 1963. Based on radiosonde and rocketsonde data, the quasibiennial temperature oscillation can be traced as high as the stratopause, the phase varying with both height and latitude. However, the rocketsonde-derived temperature decrease of several degrees Celsius in the 25–55 km layer of the Western Hemisphere between 1969 (sunspot maximum) and 1976 (sunspot minimum) is not apparent in high-level radiosonde data, so that caution is advised with respect to a possible solar-terrestrial relation.There has been a strong quasi-biennial oscillation in ozone in the 8–16 km layer of the north polar region, with ozone minimum near the time of quasi-biennial west wind maximum at a height of 20 km in the tropics. A quasi-biennial oscillation in ozone (of similar phase) is also apparent from both ozonesonde data and Umkehr measurements in 8–16 and 16–24 km layers of north temperate latitudes, but not higher up. Both measurement techniques also suggest a slight overall ozone decrease in the same layers between 1969 and 1976, but no overall ozone change in the 24–32 km layer. Umkehr measurements indicate a significant 6–8% increase in ozone amount in all stratospheric layers between 1964 and 1970, and in 1977 the ozone amount in the 32–46 km layer was still 4% above average despite the predicted depletion due to fluorocarbon emissions. The decrease in ozone in the 32–46 km, layer of mid latitudes following the volcanic eruptions of Agung and Fuego is believed to be mostly fictitious and due to the bias introduced into the Umkehr technique by stratospheric aerosols of volcanic origin. Above-average water vapor amounts in the low stratosphere at Washington, DC, appear closely related to warm tropospheric temperatures in the tropics, presumably reflecting variations in strength of the Hadley circulation.     

青藏高原对流层臭氧含量变化的太阳周期活动信号分析

利用1979~1992年卫星TOR对流层臭氧数据库资料,以及同期太阳辐照度数据序列,考察青藏高原对流层臭氧含量变化与太阳辐射周期变化之间的关系.分析表明,青藏高原对流层臭氧分布表现出与太阳辐照度相同的变化趋势,存在着明显的太阳周期变化特征.逐月线性回归分析表明,太阳辐照度增加导致青藏高原对流层臭氧增加的正效应.在太阳周期内,太阳辐射增加可使青藏高原对流层臭氧、平流层臭氧和臭氧总量分别增加1.31、4.97、6.628DU,或4.07%、2.04%、2.28%.该特征与赤道太平洋地区完全相反,分析产生差异的原因,至少应包括两方面因素：一是背景大气NO_X和水汽含量的差异;二是青藏高原频繁发生的平流层-对流层大气物质交换和输送.     

The effects of water vapour and oxides of nitrogen on ozone and temperature structure of the stratosphere

Summary A steady-state mean meridional model of the stratosphere is used to investigate the effects of water vapour and nitrogen oxides on ozone and temperature distributions in the stratosphere. The Chapman classical photochemical scheme for ozone is extended to include the dominant reactions involving hydrogen compounds and nitrogen oxides. The ozone and temperature changes are studied under radiative-photochemical equilibrium conditions and in a model incorporating both transport and radiative-photochemical processes. It is found that both hydrogen and nitrogen reactions contribute to substantial decreases in ozone and temperature under photochemical equilibrium conditions, but the computed distribution do not resemble those observed. The effect of transport processes is to reduce the deviations in the ozone mixing ratio and temperature with the computed distributions having many features in common with the observations. It is found that the ozone and temperature respond more readily to the arbitrary increase of nitrogen oxides than to that of water vapour.     

Use of coupled ozone fields in a 3-D circulation model of the middle atmosphere

With a detailed chemistry scheme for the middle atmosphere up to 70 km which has been added to the 3-D Karlsruhe simulation model of the middle atmosphere (KASIMA), the effects of coupling chemistry and dynamics through ozone are studied for the middle atmosphere. An uncoupled version using an ozone climatology for determining heating rates and a coupled version using on-line ozone are compared in a 10-month integration with meteorological analyses for the winter 1992/93 as the lower boundary condition. Both versions simulate the meteorological situation satisfactorily, but exhibit a too cold lower stratosphere. The on-line ozone differs from the climatological data between 20 and 40 km by exhibiting too high ozone values, whereas in the lower mesosphere the ozone values are too low. The coupled model version is stable and differs only above 40 km significantly from the uncoupled version. Direct heating effects are identified to cause most of the differences. The well-known negative correlation between temperature and ozone is reproduced in the model. As a result, the coupled version slightly approaches the climatological ozone field. Further feedback effects are studied by using the on-line ozone field as a basis for an artificial climatology. For non-disturbed ozone conditions realistic monthly and zonally averaged ozone data are sufficient to determine the heating rates for modelling the middle atmosphere.     

Solar response in the vertical structure of ozone and temperature in the tropical stratosphere

The aim of the present paper is to study the solar response in the vertical structure of ozone and temperature over the Indian tropical region and a search for any mutual relationship between their solar coefficients on a decadal scale in the lower stratosphere. For the purpose, the data obtained by ozonesonde and Umkehr methods for the lower stratospheric ozone and that of the total ozone amount from Dobson spectrophotometer during the period 1979–2001 have been analyzed. These data are analyzed using the multi-functional regression model, which takes into account most of the known natural and anthropogenic signals. The NCEP- and MSU-satellite data for the temperature over this region have been used. Results indicate an in-phase correlation of around 0.5 between ozone and solar flux (F10.7) in the vertical structure over the equatorial station, Trivandrum (8.3°N) but no significant correlation over Pune (18.3°N). The solar components of ozone and temperature indicate an in-phase but poor correlation in the lower stratospheric altitudes over both stations. However, when total ozone content data is analyzed, it indicates a very high correlation (⩾0.9) between the solar components of ozone and temperature. The solar trend in the vertical distribution of ozone is found to be of the order of 5–25% per 100 units of F10.7 solar flux for Trivandrum but it is relatively smaller (1.6–15.2%) over Pune. The solar dependence of temperature is found to be quite significant for the entire Indian tropical region with not much latitudinal variation.     

The average tropospheric ozone content and its variation with season and latitude as a result of the global ozone circulation

Evaluations of radiosonde soundings over North America and Europe, measurements aboard commercial airlines, and permanent ozone registrations at nineteen ground-based stations between Tromsö, Norway, and Hermanus, South Africa, yield three belts of higher ozone intrusion from the stratosphera and maximum values of the annual means at about 30°N, at between 40°–45°N and at about 60°N. A marked decrease of the annual mean values of the tropospheric ozone is detected towards the equator and the pole, respectively.In the northen hemisphere the maximum of the annual cycle of the tropospheric ozone concentration occurs in spring at high latitudes and in summer at mid-latitudes.For the tropical region from 30°S to 30°N a strong asymmetry of the northern and southern hemisphere occurs. This fact is discussed in detail. The higher troposphere of the tropics seems to be a wellmixed reservoir and mainly supplied with ozone from the tropopause gap region in the northern hemisphere. The ozone distribution in the lower troposphere of the whole tropics seems to be controlled by the up and down movements of the Hadley cell. The features of large-scale and seasonal variation of tropospheric ozone are discussed in connection with the ozone circulation in the stratosphere, the dynamic processes near the tropopause and the destruction rate at the earth's surface.     

Transport and the seasonal variation of ozone

The transport mechanisms responsible for the seasonal behavior of total ozone are deduced from the comparison of model results to stratospheric data. The seasonal transport is dominated by a combination of the diabatic circulation and transient planetary wave activity acting on a diffusively and photochemically determined background state. The seasonal variation is not correctly modeled as a diffusive process. The buildup of total ozone at high latitudes during winter is dependent upon transient planetary wave activity of sufficient strength to cause the breakdown of the polar vortex. While midwinter warmings are responsible for enhanced ozone transport to high latitudes, the final warming marking the transition from zonal mean westerlies to zonal mean easterlies is the most important event leading to the spring maximum. The final warming is not followed by reacceleration of the mean flow; so that the ozone transport associated with this event is more pronounced than that associated with midwinter warmings.