A climatological study of polar stratospheric clouds (1989–1997) from LIDAR measurements over Dumont d'Urville (Antarctica)

Backscatter lidar data from the French Antarctic base in Dumont d'Urville (66.40°S, 140.01°E), including aerosol background and observations of polar stratospheric clouds (PSCs), have been collected since 1989. In the present work we present a climatological study of PSCs, using a data base consisting of almost 90 observations. The seasonal evolution of PSCs, their optical classification, and their relationship with the observation temperature were studied. The first PSC was observed on day number 175 (15 June) and the last on day number 260 (7 September). The characteristic mid‐cloud altitude decreases through the season at a rate of 2.5 km/month. Type Ia, Ib, and II PSCs — identified by their optical properties — have been observed. External mixtures of these types have also been observed. These observations have been related to the local temperature measured by radiosondes. The relationship between PSC type and the period of the winter season was also investigated. Mixed (solid and liquid) type I clouds are mostly observed at the beginning of the winter. Type II clouds are observed only during the coldest period around midwinter, although temperatures below the frost point begin earlier and persist longer than this. Type Ia, solid‐particle, clouds are observed mostly at the end of the winter.     

Observation of polar stratospheric clouds over Obninsk in December 2012

In late December 2012 a blocking anticyclone followed by the event of minor stratospheric warming, set in the troposphere over West Siberia and, after that, over the European part of Russia. As a result of the deformation of a polar stratospheric vortex, the temperature in the lower stratosphere over Obninsk dropped below the threshold of the formation of polar stratospheric clouds. The lidar measurements of temperature, ozone values, and aerosol characteristics in the middle atmosphere were carried out at the lidar station during this atmospheric event. In three cases, polar stratospheric clouds (PSCs) referred to NAT I_a type according to the sounding results, were registered at the height of about 20 km. No considerable decrease in the ozone concentration in the area of PSC formation was revealed in these measurements.     

Characteristics of cirrus clouds and its radiative properties based on lidar observation over Chung-Li, Taiwan

In this paper, characterization of cirrus clouds are made by using data from ground based polarization lidar and radiosonde measurements over Chung-Li (24.58°N, 121.10°E), Taiwan for a period of 1999–2006. During this period, the occurrence of cirrus clouds is about 37% of the total measurement nights over the lidar site. Analysis of the measurement gives the statistical characteristics about the macrophysical properties such as occurrence height, ambient temperature, and its geometrical thickness while the microphysical properties are interpreted in terms of extinction coefficient, optical depth, effective lidar ratio and depolarization ratio. The effective lidar ratio has been retrieved by using the simulation technique of backscattered lidar signals. The effect of multiple scattering has been taken into the account by a model calculation. Summer (Jun–Aug) shows the maximum appearances of cirrus due to its formation mechanism. It is shown that tropopause cirrus clouds may occur with a probability of about 24%. These clouds are usually optically thin and having laminar in structure with some cases resembling the characteristics similar to that of polar stratospheric clouds (PSCs). The radiative properties of the cirrus clouds are also discussed in detail by the empirical equations with results show a positive feedback on any climate change.     

The impact of high altitude aircraft on the ozone layer in the stratosphere

The paper discusses the potential effects on the ozone layer of gases released by the engines of proposed high altitude supersonic aircraft. The major problem arises from the emissions of nitrogen oxides which have the potential to destroy significant quantities of ozone in the stratosphere. The magnitude of the perturbation is highly dependent on the cruise altitude of the aircraft. Furthermore, the depletion of ozone is substantially reduced when heterogeneous conversion of nitrogen oxides into nitric acid on sulfate aerosol particles is taken into account in the calculation. The sensitivity of the aerosol load on stratospheric ozone is investigated. First, the model indicates that the aerosol load induced by the SO₂ released by aircraft is increased by about 10–20% above the background aerosols at mid-high latitude of the Northern Hemisphere at 15 km for the NASA emission scenario A (the NASA emission scenarios are explained in Tables I to III). This increase in aerosol has small effects on stratospheric ozone. Second, when the aerosol load is increased following a volcanic eruption similar to the eruption of El Chichon (Mexico, April 1982), the ozone column in spring increases by as much as 9% in response to the injection of NO _x from the aircraft with the NASA emission scenario A. Finally, the modeled suggests that significant ozone depletion could result from the formation of additional polar stratospheric clouds produced by the injection of H₂O and HNO₃ by the aircraft engines.     

HNO3 and PSC Measurements from the Transall: Sequestering of HNO3 in the Winter of 1994/95

In the winter of 1994/95 the TRANSALL research aircraft performed several flights in the region of the Arctic vortex during the period of low stratospheric temperatures. The results of simultaneous measurements of HNO3 column amounts by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) and of aerosol backscatter profiles by the Ozone Lidar EXperiment (OLEX) are presented for two typical flight scenarios across the polar vortex boundary on December 17, 1994 and January 11/12, 1995. On December 17 and January 12, the column amounts of gaseous HNO3 decreased significantly in regions with low stratospheric temperatures. This decrease was correlated with the extent of the polar stratospheric clouds. Depolarisation measurements showed that type Ib PSCs were observed primarily, but equilibrium calculations for H2SO4/HNO3/H2O aerosols seem to underestimate the observed HNO3 sequestering.     

Nitrosyl and Nitryl Chloride Formation in H2SO4/HNO3/H2O/HCl Solutions at 200 K

Infrared spectroscopy has been used to measure the vapor pressure of chlorine containing species generated from H2SO4/HNO3/H2O/HCl solutions at 200 K. The vapor pressure was observed to be a function of solution composition. Two solution compositions were investigated. One solution remained a liquid whereas the second solution was a mixed liquid and solid phase (an ice slurry). The liquid solution had a composition of 64.6 wt.% H2SO4/4.8 wt.% HNO3/30.1 wt.% H2O/0.5 wt.% HCl and produced only vapor phase HCl. The ice slurry solution had a composition of 76.6 wt.% H2SO4/3.0 wt.% HNO3/20.1 wt.% H2O/0.3 wt.% HCl and produced HCl, ClNO, and ClNO2 vapor phase components. The sulfuric acid, nitric acid, and water content of these solutions are representative of those present in polar stratospheric clouds (PSCs), however the HCl concentrations are much higher than present within these clouds. The partitioning of chlorine between vapor phase HCl (50%) and ClNO/ClNO2 (50%) for the ice slurry solution suggests a possible mechanism of halogen activation within PSCs. A reaction mechanism to model the observed chemistry is proposed.     

On the growth of nitric and sulfuric acid aerosol particles under stratospheric conditions

We present a theory for the formation of frozen aerosol particles in the Antarctic stratosphere, the coldest region of the Earth's stratosphere. The theory is applied specifically to the formation of polar stratospheric clouds. We suggest that the condensed ices are composed primarily of nitric acid and water with small admixtures of other compounds such as H₂SO₄ and HCl in solid solution. Our assumed particle formation mechanism is in agreement with the magnitude and seasonal behavior of the optical extinctions observed in the winter polar stratosphere. Physical chemistry and thermodynamic considerations suggest that at temperatures between about 200 and 185 K, stratospheric particulates are composed primarily of frozen nitric acid solutions with a composition near that of the trihydrate. Available data suggest the particles are amorphous solid solutions and not in the crystalline hydrate form. At lower temperatures (i.e., below the forst point of pure water) cirrus-like ice clouds can form.     

Validation of a limited area model over Dome C, Antarctic Plateau, during winter

The limited area model MAR (Modèle Atmosphérique Régional) is validated over the Antarctic Plateau for the period 2004–2006, focussing on Dome C during the cold season. MAR simulations are made by initializing the model once and by forcing it through its lateral and top boundaries by the ECMWF operational analyses. Model outputs compare favourably with observations from automatic weather station (AWS), radiometers and atmospheric soundings. MAR is able to simulate the succession of cold and warm events which occur at Dome C during winter. Larger longwave downwelling fluxes (LWD) are responsible for higher surface air temperatures and weaker surface inversions during winter. Warm events are better simulated when the small Antarctic precipitating snow particles are taken into account in radiative transfer computations. MAR stratosphere cools during the cold season, with the coldest temperatures occurring in conjunction with warm events at the surface. The decrease of saturation specific humidity associated with these coldest temperatures is responsible for the formation of polar stratospheric clouds (PSCs) especially in August-September. PSCs then contribute to the surface warming by increasing the surface downwelling longwave flux.     

Meteorological conditions and polar stratospheric clouds over Yakutsk in winter 2004/05

Regular observations of polar stratospheric clouds were started at a lidar stratospheric station in the city of Yakutsk. According to lidar measurements in the winter of 2004/05, thick aerosol layers in the lower stratosphere appeared over this region quite frequently. They were episodically observed as pearl clouds. In November 2004, polar stratospheric clouds were observed at the stratospheric temperatures that were much higher than those at which particles of the polar stratospheric clouds could condense. Analysis of air-mass trajectories that simultaneously passed over Yakutsk at different altitudes on the days of polar stratospheric cloud observations showed that clouds could be formed over the Norwegian Sea at altitudes of about 18–21 km, where the stratosphere was the coldest, and then were transported to Yakutsk by wind during 4–5 days.     

Numerical Modeling of the Influence of Physical and Chemical Factors on the Interannual Variability of Antarctic Ozone

The variability of Antarctic total column ozone in 1980–2018 is considered. The study analyzes trends in Antarctic total column ozone during the study period as well as the physical and chemical processes affecting the seasonal variability of total column ozone. The main attention is paid to the influence of dynamical processes on the stability of the Antarctic polar vortex, to the formation of polar stratospheric clouds, and to the influence of gas-phase and heterogeneous processes on the surface of polar stratospheric clouds and sulfate aerosol. The method of research is the analysis of the results of ground and satellite observations and numerical modeling of physical and chemical processes over the Antarctic using a global chemistry transport model with the dynamical parameters specified from reanalysis data.     

Extremely low temperatures in the stratosphore and very low total ozone amount above northern and central Europe during winter 1989

On 1 February 1989, -83.5°C was recorded in 27.8 hPa over Hohenpeißenberg, the lowest temperature in the 22-year series. This was measured together with a very low total ozone amount of 266 DU. This may be compared with nearly twice this amount on 27 February 1989. The situation was very unusual: following an extremely cold winter in the Arctic stratosphere, the stratospheric cold pole was located over southern Scandinavia on 1 February in a very southerly position. The analyzed temperatures of -92 °C in 30 hPa were also unusual. Even though the low ozone amounts over Hohenpeißenberg were probably dynamically caused, an additional very small ozone decrease due to heterogeneous reactions in altitudes from 23–28 km, where the temperatures lie below -80 °C, cannot be ruled out. Extinction measurements by the orbitting SAGE II instrument indeed show polar stratospheric clouds over Europe near 50° N during the period 31 January–2 February. Also, polar stratospheric clouds were previously observed over Kiruna at similarly low temperatures and signs of a corresponding small ozone decrease were noted there.     

A review of global stratospheric aerosol: Measurements, importance, life cycle, and local stratospheric aerosol

Stratospheric aerosol, noted after large volcanic eruptions since at least the late 1800s, were first measured in the late 1950s, with the modern continuous record beginning in the 1970s. Stratospheric aerosol, both volcanic and non-volcanic are sulfuric acid droplets with radii (concentrations) on the order of 0.1–0.5 µm (0.5–0.005 cm^− 3), increasing by factors of 2–4 (10–10³) after large volcanic eruptions. The source of the sulfur for the aerosol is either through direct injection from sulfur-rich volcanic eruptions, or from tropical injection of tropospheric air containing OCS, SO₂, and sulfate particles. The life cycle of non-volcanic stratospheric aerosol, consisting of photo-dissociation and oxidation of sulfur source gases, nucleation/condensation in the tropics, transport pole-ward and downward in the global planetary wave driven tropical pump, leads to a quasi steady state relative maximum in particle number concentration at around 20 km in the mid latitudes. Stratospheric aerosol have significant impacts on the Earth's radiation balance for several years following volcanic eruptions. Away from large eruptions, the direct radiation impact is small and well characterized; however, these particles also may play a role in the nucleation of near tropopause cirrus, and thus indirectly affect radiation. Stratospheric aerosol play a larger role in the chemical, particularly ozone, balance of the stratosphere. In the mid latitudes they interact with both nitrous oxides and chlorine reservoirs, thus indirectly affecting ozone. In the polar regions they provide condensation sites for polar stratospheric clouds which then provide the surfaces necessary to convert inactive to active chlorine leading to polar ozone loss. Until the mid 1990s the modern record has been dominated by three large sulfur-rich eruptions: Fuego (1974), El Chichón (1982) and Pinatubo (1991), thus definitive conclusions concerning the trend of non-volcanic stratospheric aerosol could only recently be made. Although anthropogenic emissions of SO₂ have changed somewhat over the past 30 years, the measurements during volcanically quiescent periods indicate no long term trend in non-volcanic stratospheric aerosol.     

Intercomparison of Stratospheric Chemistry Models under Polar Vortex Conditions

Several stratospheric chemistry modules from box, 2-D or 3-D models, have been intercompared. The intercomparison was focused on the ozone loss and associated reactive species under the conditions found in the cold, wintertime Arctic and Antarctic vortices. Comparisons of both gas phase and heterogeneous chemistry modules show excellent agreement between the models under constrained conditions for photolysis and the microphysics of polar stratospheric clouds. While the mean integral ozone loss ranges from 4–80% for different 30–50 days long air parcel trajectories, the mean scatter of model results around these values is only about ±1.5%. In a case study, where the models employed their standard photolysis and microphysical schemes, the variation around the mean percentage ozone loss increases to about ±7%. This increased scatter of model results is mainly due to the different treatment of the PSC microphysics and heterogeneous chemistry in the models, whereby the most unrealistic assumptions about PSC processes consequently lead to the least representative ozone chemistry. Furthermore, for this case study the model results for the ozone mixing ratios at different altitudes were compared with a measured ozone profile to investigate the extent to which models reproduce the stratospheric ozone losses. It was found that mainly in the height range of strong ozone depletion all models underestimate the ozone loss by about a factor of two. This finding corroborates earlier studies and implies a general deficiency in our understanding of the stratospheric ozone loss chemistry rather than a specific problem related to a particular model simulation.     

BCC_AGCM2.1模式对平流层环流变化特征的数值模拟及其模式评估

使用国家气候中心大气环流模式BCC_AGCM2.1的30年模拟试验资料,对平流层纬向环流场、高空急流、极涡及爆发性增温过程进行了数值模拟研究,并使用欧洲中期天气预报中心（ECMWF）和美国国家环境预报中心（NCEP）的再分析资料对模式输出结果进行了对比、分析。结果表明：（1） 在观测海温、二氧化碳、气溶胶等外强迫地驱动下,BCC模式能够很好地再现出与再分析资料一致的平流层纬向平均风场、温度场的分布特征和季节变化过程;模拟得到的温度廓线和高空急流与再分析资料的主要差别出现在南、北半球冬季的中高纬度地区;模拟得到的平流层温度普遍偏低,主要的差异位于对流层顶区域和平流层高层。（2） 模拟的对流层上层的副热带急流位置偏南、强度也偏弱,而平流层中的绕极极夜急流则位置偏北、强度更大。这样的急流分布特征使模拟的行星波向赤道的波导更强,向极的波导偏弱;同时由于模式中本身可以形成的行星波就比再分析资料弱,因此导致模拟结果中北半球冬季的平流层极涡更加稳定、极区温度更低。（3） BCC模式对于平流层极涡的季节变化特征模拟得较好,但对强极涡扰动过程,即北半球冬季的平流层爆发性增温（SSW）事件则模拟效果不佳,不论是增温事件出现的频率,还是增温的时间、强度,模拟结果和再分析资料都还存在一定偏差,需要在今后的工作中逐步改善。     

Carbonyl Sulphide (OCS) Variability with Latitude in the Atmosphere

Abstract

Carbonyl sulphide (OCS) is an important precursor of sulphate aerosols and consequently a key species in stratospheric ozone depletion. The SPectromètre InfraRouge d'Absorption à Lasers Embarqués (SPIRALE) and shortwave infrared (SWIR) balloon-borne instruments have flown in the tropics and in the polar Arctic, and ground-based measurements have been performed by the Qualité de l'Air (QualAir) Fourier Transform Spectrometer in Paris. Partial and total columns and vertical profiles have been obtained to study OCS variability with altitude, latitude, and season. The annual total column variation in Paris reveals a seasonal variation with a maximum in April–June and a minimum in November–January. Total column measurements above Paris and from SWIR balloon-borne instrument are compared with several MkIV measurements, several Network for the Detection of Atmospheric Composition Change (NDACC) stations, aircraft, ship, and balloon measurements to highlight the OCS total column decrease from tropical to polar latitudes. OCS high-resolution in situ vertical profiles have been measured for the first time in the altitude range between 14 and 30?km at tropical and polar latitudes. OCS profiles are compared with Atmospheric Chemistry Experiment (ACE) satellite measurements and show good agreement. Using the correlation between OCS and N₂O from SPIRALE, the OCS stratospheric lifetime has been accurately determined. We find a stratospheric lifetime of 68?±?20 years at polar latitudes and 58?±?14 years at tropical latitudes leading to a global stratospheric sink of 49?±?14?Gg?S?y^?1.     

Uncertainty of AMSU-A derived temperature trends in relationship with clouds and precipitation over ocean

Microwave Sounding Unit (MSU) and Advanced Microwave Sounding Unit-A (AMSU-A) observations from a series of National Oceanic and Atmospheric Administration satellites have been extensively utilized for estimating the atmospheric temperature trend. For a given atmospheric temperature condition, the emission and scattering of clouds and precipitation modulate MSU and AMSU-A brightness temperatures. In this study, the effects of the radiation from clouds and precipitation on AMSU-A derived atmospheric temperature trend are assessed using the information from AMSU-A window channels. It is shown that the global mean temperature in the low and middle troposphere has a larger warming rate (about 20–30 % higher) when the cloud-affected radiances are removed from AMSU-A data. It is also shown that the inclusion of cloud-affected radiances in the trend analysis can significantly offset the stratospheric cooling represented by AMSU-A channel 9 over the middle and high latitudes of Northern Hemisphere.     

Interannual variability of the winter stratospheric polar vortex in the Northern Hemisphere and their relations to QBO and ENSO

We investigated the interannual variations of the winter stratospheric polar vortex in this paper. EOF analysis shows that two modes of variability dominate the stratospheric polar vortex on interannual timescales. The leading mode (EOF1) reflects the intensity variation of the polar vortex and is characterized by a geopotential height seesaw between the polar region and the mid-latitudes. The second one (EOF2) exhibits variation in the zonal asymmetric part of the polar vortex, which mainly describes the stationary planetary wave activity. As the strongest interannual variation signal in the atmosphere, the QBO has been shown to influence mainly the strength of the polar vortex. On the other hand, the ENSO cycle, as the strongest interannual variation signal in the ocean, has been shown to be mainly associated with the variation of stationary planetary wave activity in the stratosphere. Possible influences of the stratospheric polar vortex on the tropospheric circulation are also discussed in this paper.     

Possible mechanism of ozone depletion on ice crystals in the polar stratosphere

Developed is a new mechanism of photochemical reactions taking account of the dipole interaction between the molecules and the ??sharp?? inhomogeneities of electrified ice crystals in polar stratospheric clouds. This mechanism enables to explain the ozone depression formation during the winter-spring period in the polar stratosphere.     

Aircraft measurements and model simulations of stratospheric ozone and N2O: implications for chemistry and transport processes in the models

Airborne measurements of stratospheric ozone and N₂O from the SCIAMACHY (Scanning Imaging Absorption Spectrometer) Validation and Utilization Experiment (SCIA-VALUE) are presented. The campaign was conducted in September 2002 and February–March 2003. The Airborne Submillimeter Radiometer (ASUR) observed stratospheric constituents like O₃ and N₂O, among others, spanning a latitude from 5°S to 80°N during the survey. The tropical ozone source regions show high ozone volume mixing ratios (VMRs) of around 11 ppmv at 33 km altitude, and the altitude of the maximum VMR increases from the tropics to the Arctic. The N₂O VMRs show the largest value of 325 ppbv in the lower stratosphere, indicating their tropospheric origin, and they decrease with increasing altitude and latitude due to photolysis. The sub-tropical and polar mixing barriers are well represented in the N₂O measurements. The most striking seasonal difference found in the measurements is the large polar descent in February–March. The observed features are interpreted with the help of SLIMCAT and Bremen Chemical Transport Model (CTMB) simulations. The SLIMCAT simulations are in good agreement with the measured O₃ and N₂O values, where the differences are within 1 ppmv for O₃ and 15 ppbv for N₂O. However, the CTMB simulations underestimate the tropical middle stratospheric O₃ (1–1.5 ppmv) and the tropical lower stratospheric N₂O (15–30 ppbv) measurements. A detailed analysis with various measurements and model simulations suggests that the biases in the CTMB simulations are related to its parameterised chemistry schemes.