Analysis of the variations in the strength and position of stratospheric sudden warming in the past three decades

利用ERA-Interim再分析资料统计分析了1920–2016年期间北半球33次强平流层爆发性增温(SSW)事件和22次弱增温事件的强度和位置变化特征。发现SSW主要发生在二月,其纬向平均温度的最大经向梯度变化在1979–8319年和1998–2011年呈上升趋势,1984–1997年和2012–2016年呈下降趋势,但是整体呈现略微下降的线性趋势,并且强SSW事件的强度和持续时间的变化特征相似。一些SSW事件几乎同时在100 hPa到10 hPa上出现,一些SSW事件却首先出现在10 hPa上再向低层下传。另外,我们还发现这55个SSW事件的最大增温中心主要位于欧亚大陆30°E到120°E之间,这或许跟过去三十年中欧亚大陆的极涡转移有关。     

Emission scenarios for a global hydrogen economy and the consequences for global air pollution

Hydrogen is named as possible energy carrier for future energy systems. However, the impact of large-scale hydrogen use on the atmosphere is uncertain. Application of hydrogen in clean fuel cells reduces emissions of air pollutants, but emissions from hydrogen production and leakages of molecular hydrogen could influence atmospheric chemistry. This paper combines a global energy system model and a global atmospheric model to explore the range of impacts of hydrogen on atmospheric chemistry. We found that emissions of molecular hydrogen may range from 0.2 up to 10% (or 25-167 Tg hydrogen/yr) for a global hydrogen energy system. The lower end of this range would in fact be equal to current emissions from fossil fuel combustion. Hydrogen energy use leads to a clear decrease in emissions of carbon monoxide, nitrogen oxides and sulphur dioxide, but large-scale hydrogen production from coal may lead to net increase in emissions of nitrous oxide and volatile organic compound. Compared to a reference scenario, this would lead to positive impacts on surface concentrations of carbon monoxide, nitrogen oxides and ozone. However, if hydrogen leakage would not be minimised it leads to an increase in methane lifetimes and a decrease in stratospheric ozone concentrations.     

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.     

N2O增加对大气环境影响的模拟及其与甲烷和平流层水汽影响的比较

本文利用美国国家大气环境中心(NCAR)的二维化学、辐射和动力相互作用的模式(SOCRATES),模拟了大气中N₂O增加对O₃和温度的影响,并从化学、辐射和动力过程讨论了影响原因,此外还与大气甲烷和平流层水汽增加对大气环境的影响进行了对比.分析表明:大气中N₂O浓度增加以后,将通过化学过程引起30 km以上O₃损耗,30~40 km损耗较多;30 km以上降温明显,下平流层中低纬度地区以及对流层O₃增加并有微弱升温;30~40 km附近,北半球中高纬地区O₃减少以及降温幅度都大于南半球.对流层升温主要是N₂O和O₃增加所致,而平流层温度变化主要受O₃控制.北半球中高纬地区动力过程对温度变化的反馈较其它地区明显,这种反馈对平流层中高层北半球中高纬地区温度和O₃的变化都有明显影响.大气中甲烷增加引起的O₃损耗在45 km以上,45 km以下O₃增加.平流层水汽增加会引起40 km以上O₃减少,20~40 km大部分地区O₃增加.N₂O增加造成的O₃损耗正好位于臭氧层附近,其排放对未来O₃层恢复至关重要.N₂O增加引起下平流层15~25 km中低纬度地区有弱的升温,这与其它温室气体增加对该地区温度的影响不同,CO₂,CH₄和H₂O等增加后下平流层通常是降温.     

Springtime effects in the mesosphere and ionosphere observed at northern midlatitudes

Nighttime volume emission rates and rotational temperatures, obtained from simultaneous observations of molecular oxygen and hydroxyl airglow at Almaty (43.25°N, 76.92°E) and Sierra-Nevada (37.2°N, 356.7°E), along with ionospheric density derived from foF2 in the vertical sounding ionograms over Almaty are analysed to study the variability and coupling of parameters observed in the upper mesosphere and ionosphere during the period of February - April, 2000.Ionospheric critical frequency measurements and airglow observations by the Mesopause Rotational Temperature Imager (MORTI) at Almaty and the Spectral Airglow Temperature Imager (SATI) at Sierra-Nevada Observatories show an increase in long-period planetary wave (PW) activity from the end of February until the middle of March, 2000.Very good agreement was found in the temporal variations of emission rates and rotational temperatures from March 1-15, 2000 measured at the Almaty and Sierra-Nevada sites. Similar perturbations could also be seen in the ionospheric critical frequency (ΔfoF2) obtained as a difference between current foF2 values and an ionospheric background level.The perturbations observed have been interpreted employing the Met office stratospheric model results. Latitudinal structure of a quasi 5-day wave was identified, for which the first-symmetric-mode amplitude and symmetric behaviour of phase are in good agreement with theoretical prediction. The analysis of the Met office stratospheric data indicate the presence of westward-propagating PW with periods of ∼5 and 10 days during the period of interest. The temporal correlation between planetary scale oscillations observed in the datasets examined (ionospheric, optical and meteorological) suggest dynamical coupling with the stratosphere. A negative disturbance in ΔfoF2 of ∼25% observed 1 day before a sharp increase in the MORTI mesospheric rotational temperature registered on March 10 at Almaty, is also discussed in the context of the possible stratosphere/mesosphere/ionosphere coupling.     

平流层臭氧的温室效应及其气候影响

本文阐述大气中重要的“痕量气体”之一——臭氧(平流层臭氧)对地球表面和低层大气的温室效应及其全球气候的反馈影响;指出了云的辐射力的概念及其重要性,并讨论了“南极臭氧洞”现象。     

High resolution simulation of recent Arctic and Antarctic stratospheric chemical ozone loss compared to observations

Simulations of polar ozone losses were performed using the three-dimensional high-resolution (1^∘ × 1^∘) chemical transport model MIMOSA-CHIM. Three Arctic winters 1999–2000, 2001–2002, 2002–2003 and three Antarctic winters 2001, 2002, and 2003 were considered for the study. The cumulative ozone loss in the Arctic winter 2002–2003 reached around 35% at 475 K inside the vortex, as compared to more than 60% in 1999–2000. During 1999–2000, denitrification induces a maximum of about 23% extra ozone loss at 475 K as compared to 17% in 2002–2003. Unlike these two colder Arctic winters, the 2001–2002 Arctic was warmer and did not experience much ozone loss. Sensitivity tests showed that the chosen resolution of 1^∘ × 1^∘ provides a better evaluation of ozone loss at the edge of the polar vortex in high solar zenith angle conditions. The simulation results for ozone, ClO, HNO₃, N₂O, and NO _y for winters 1999–2000 and 2002–2003 were compared with measurements on board ER-2 and Geophysica aircraft respectively. Sensitivity tests showed that increasing heating rates calculated by the model by 50% and doubling the PSC (Polar Stratospheric Clouds) particle density (from 5 × 10⁻³ to 10⁻² cm⁻³) refines the agreement with in situ ozone, N₂O and NO _y levels. In this configuration, simulated ClO levels are increased and are in better agreement with observations in January but are overestimated by about 20% in March. The use of the Burkholder et al. (1990) Cl₂O₂ absorption cross-sections slightly increases further ClO levels especially in high solar zenith angle conditions. Comparisons of the modelled ozone values with ozonesonde measurement in the Antarctic winter 2003 and with Polar Ozone and Aerosol Measurement III (POAM III) measurements in the Antarctic winters 2001 and 2002, shows that the simulations underestimate the ozone loss rate at the end of the ozone destruction period. A slightly better agreement is obtained with the use of Burkholder et al. (1990) Cl₂O₂ absorption cross-sections.     

The evolution of Pinatubo aerosols in the Arctic stratosphere during 1994–2000

Balloon-borne aerosol measurements were performed with an optical particle counter between 1994 and 2000 at Ny-Ålesund (79°N), Svarbard. Throughout the observation period, continuous decay was found in the concentrations of particles with 0.4–0.6 μm in radius in the Arctic stratosphere, suggesting that Pinatubo aerosols remained even at the end of the 1990s. The decay rate was clearly higher for larger particle sizes, and higher at higher altitude (e-folding time of 970–526 days), suggesting a gravitational sedimentation effect. For smaller particles with R<0.4 μm, slight increases in concentration with time were found, which agreed with the measurements at mid-latitude. The sulfate mass mixing ratio in the Arctic stratosphere before 1998 showed values higher than those at middle latitude, while values were almost the same in both regions after 1998. A possible explanation of the latitudinal difference is a time lag (of 0.5–1 year) in the arrival of Pinatubo aerosols in the Arctic.     

The vertical distribution of CFM and related species in the stratosphere

Available data on halogenated molecules in the stratosphere will be reviewed. Presently vertical profiles of CFCl₃ and CF₂Cl₂ in the stratosphere exist to 50 km altitude. Only measurements in the lower stratosphere are reported for the other major halocarbons, CCl₄ and CH₃Cl. Profiles of the product species ClO, Cl, HCl, and HF exist to about 35 km.Comparison with theoretical profiles from 1-D models shows generally good agreement except for ClO where the earliest measured concentrations exceed the calculated ones considerably.     

Stratospheric ozone response to a solar proton event: Hemispheric asymmetries

Ozone depression in the polar stratosphere during the energetic solar proton event on 4 August 1972 was observed by the backscattered ultraviolet (BUV) experiment on the Nimbus 4 satellite. Distinct asymmetries in the columnar ozone content, the amount of ozone depressions and their temporal variations above 4 mb level (38 km) were observed between the two hemispheres. The ozone destroying solar particles precipitate rather symmetrically into the two polar atmospheres due to the geomagnetic dipole field These asymmetries can be therefore ascribed to the differences mainly in dynamics and partly in the solar illumination and the vertical temperature structure between the summer and the winter polar atmospheres. The polar stratosphere is less disturbed and warmer in the summer hemisphere than the winter hemisphere since the propagation of planetary wave from the troposphere is inhibited by the wind system in the upper troposphere, and the air is heated by the prolonged solar insolation. Correspondingly, the temporal variations of stratospheric ozone depletion and its recovery appear to be smooth functions of time in the (northern) summer hemisphere and the undisturbed ozone amount is slighily, less than that of its counterpart. On the other hand, the tempotal variation of the upper stratospheric ozone in the winter polar atmosphere (southern hemisphere) indicates large amplitudes and irregularities due to the disturbances produced by upward propagating waves which prevail in the polar winter atmosphere. These characteristic differences between the two polar atmospheres are also evident in the vertical distributions of temperature and wind observed by balloons and rocker soundings.