Sophie Godin-Beekmann

The Untold Story of Pyrocumulonimbus

Wildfire is becoming the focus of increasing attention. It is now realized that changes in the occurrence frequency and intensity of wildfires has important significant consequences for a variety of important problems, including atmospheric change and safety in the urban–wildland interface. One important but poorly understood aspect of wildfire behavior—pyrocumulonimbus firestorm dynamics and atmospheric impact—has a curious history of theory and observation. The “pyroCb” is a fire-started or fire-augmented thunderstorm that in its most extreme manifestation injects huge abundances of smoke and other biomass-burning emissions into the lower stratosphere. The observed hemispheric spread of smoke and other biomass-burning emissions could have important climate consequences. PyroCbs have been spawned naturally and through anthropogenesis, and they are hypothesized as being part of the theoretical “Nuclear nuclear winter” work. However, direct attribution of the stratospheric aerosols to the pyroCb only occur...

Validation of Aura Microwave Limb Sounder Ozone by ozonesonde and lidar measurements

We present validation studies of MLS version 2.2 upper tropospheric and stratospheric ozone profiles using ozonesonde and lidar data as well as climatological data. Ozone measurements from over 60 ozonesonde stations worldwide and three lidar stations are compared with coincident MLS data. The MLS ozone stratospheric data between 150 and 3 hPa agree well with ozonesonde measurements, within 8% for the global average. MLS values at 215 hPa are biased high compared to ozonesondes by A`20% at middle to high latitude, although there is a lot of variability in this altitude region. Comparisons between MLS and ground-based lidar measurements from Mauna Loa, Hawaii, from the Table Mountain Facility, California, and from the Observatoire de Haute-Provence, France, give very good agreement, within A`5%, for the stratospheric values. The comparisons between MLS and the Table Mountain Facility tropospheric ozone lidar show that MLS data are biased high by A`30% at 215 hPa, consistent with that indicated by the ozonesonde data. We obtain better global average agreement between MLS and ozonesonde partial column values down to 215 hPa, although the average MLS values at low to middle latitudes are higher than the ozonesonde values by up to a few percent. MLS v2.2 ozone data agree better than the MLS v1.5 data with ozonesonde and lidar measurements. MLS tropical data show the wave one longitudinal pattern in the upper troposphere, with similarities to the average distribution from ozonesondes. High upper tropospheric ozone values are also observed by MLS in the tropical Pacific from June to November.

A trajectory-based estimate of the tropospheric ozone column using the residual method

We estimate the tropospheric column ozone using a forward trajectory model to increase the horizontal resolution of the Aura Microwave Limb Sounder (MLS) derived stratospheric column ozone. Subtracting the MLS stratospheric column from Ozone Monitoring Instrument total column measurements gives the trajectory enhanced tropospheric ozone residual (TTOR). Because of different tropopause definitions, we validate the basic residual technique by computing the 200-hPa-to-surface column and comparing it to the same product from ozonesondes and Tropospheric Emission Spectrometer measurements. Comparisons show good agreement in the tropics and reasonable agreement at middle latitudes, but there is a persistent low bias in the TTOR that may be due to a slight high bias in MLS stratospheric column. With the improved stratospheric column resolution, we note a strong correlation of extratropical tropospheric ozone column anomalies with probable troposphere-stratosphere exchange events or folds. The folds can be identified by their colocation with strong horizontal tropopause gradients. TTOR anomalies due to folds may be mistaken for pollution events since folds often occur in the Atlantic and Pacific pollution corridors. We also compare the 200-hPa-to-surface column with Global Modeling Initiative chemical model estimates of the same quantity. While the tropical comparisons are good, we note that chemical model variations in 200-hPa-to-surface column at middle latitudes are much smaller than seen in the TTOR.

Ozone and temperature trends in the upper stratosphere at five stations of the Network for the Detection of Atmospheric Composition Change

Upper stratospheric ozone anomalies from the satellite-borne Solar Backscatter Ultra-Violet (SBUV), Stratospheric Aerosol and Gas Experiment II (SAGE II), Halogen Occultation Experiment (HALOE), Global Ozone Monitoring by Occultation of Stars (GOMOS), and Scanning Imaging Absorption Spectrometer for Atmospheric Chartography (SCIAMACHY) instruments agree within 5% or better with ground-based data from lidars and microwave radiometers at five stations of the Network for the Detection of Atmospheric Composition Change (NDACC), from 45°S to 48°N. From 1979 until the late 1990s, all available data show a clear decline of ozone near 40 km, by 10%–15%. This decline has not continued in the last 10 years. At some sites, ozone at 40 km appears to have increased since 2000, consistent with the beginning decline of stratospheric chlorine. The phaseout of chlorofluorocarbons after the International Montreal Protocol in 1987 has been successful, and is now showing positive effects on ozone in the upper stratosphere. Temperature anomalies near 40 km altitude from European Centre for Medium Range Weather Forecast reanalyses (ERA-40), from National Centers for Environmental Prediction (NCEP) operational analyses, and from HALOE and lidar measurements show good consistency at the five stations, within about 3 K. Since about 1985, upper stratospheric temperatures have been fluctuating around a constant level at all five NDACC stations. This non-decline of upper stratospheric temperatures is a significant change from the more or less linear cooling of the upper stratosphere up until the mid-1990s, reported in previous trend assessments. It is also at odds with the almost linear 1 K per decade cooling simulated over the entire 1979–2010 period by chemistry–climate models (CCMs). The same CCM simulations, however, track the historical ozone anomalies quite well, including the change of ozone tendency in the late 1990s.

Toward a better quantitative understanding of polar stratospheric ozone loss

Previous studies have shown that observed large O3 loss rates in cold Arctic Januaries cannot be explained with current understanding of the loss processes, recommended reaction kinetics, and standard assumptions about total stratospheric chlorine and bromine. Studies based on data collected during recent field campaigns suggest faster rates of photolysis and thermal decomposition of ClOOCl and higher stratospheric bromine concentrations than previously assumed. We show that a model accounting for these kinetic changes and higher levels of BrO can largely resolve the January Arctic O3 loss problem and closely reproduces observed Arctic O3 loss while being consistent with observed levels of ClO and ClOOCl. The model also suggests that bromine catalysed O3 loss is more important relative to chlorine catalysed loss than previously thought.

Stratospheric AOD after the 2011 eruption of Nabro volcano measured by lidars over the Northern Hemisphere

Nabro volcano (13.37°N, 41.70°E) in Eritrea erupted on 13 June 2011 generating a layer of sulfate aerosols that persisted in the stratosphere for months. For the first time we report on ground-based lidar observations of the same event from every continent in the Northern Hemisphere, taking advantage of the synergy between global lidar networks such as EARLINET, MPLNET and NDACC with independent lidar groups and satellite CALIPSO to track the evolution of the stratospheric aerosol layer in various parts of the globe. The globally averaged aerosol optical depth (AOD) due to the stratospheric volcanic aerosol layers was of the order of 0.018 ± 0.009 at 532 nm, ranging from 0.003 to 0.04. Compared to the total column AOD from the available collocated AERONET stations, the stratospheric contribution varied from 2% to 23% at 532 nm.

Initial validation of ozone measurements from the High Resolution Dynamics Limb Sounder

Comparisons of the latest High Resolution Dynamics Limb Sounder (HIRDLS) ozone retrievals (v2.04.09) are made with ozonesondes, ground-based lidars, airborne lidar measurements made during the Intercontinental Chemical Transport Experiment–B, and satellite observations. A large visual obstruction blocking over 80% of the HIRDLS field of view presents significant challenges to the data analysis methods and implementation, to the extent that the radiative properties of the obstruction must be accurately characterized in order to adequately correct measured radiances. The radiance correction algorithms updated as of August 2007 are used in the HIRDLS v2.04.09 data presented here. Comparisons indicate that HIRDLS ozone is recoverable between 1 and 100 hPa at middle and high latitudes and between 1 and 50 hPa at low latitudes. Accuracy of better than 10% is indicated between 1 and 30 hPa (HIRDLS generally low) by the majority of the comparisons with coincident measurements, and 5% is indicated between 2 and 10 hPa when compared with some lidars. Between 50 and 100 hPa, at middle and high latitudes, accuracy is 10–20%. The ozone precision is estimated to be generally 5–10% between 1 and 50 hPa. Comparisons with ozonesondes and lidars give strong indication that HIRDLS is capable of resolving fine vertical ozone features (1–2 km) in the region between 1 and 50 hPa. Development is continuing on the radiance correction and the cloud detection and filtering algorithms, and it is hoped that it will be possible to achieve a further reduction in the systematic bias and an increase in the measurement range downward to lower heights (at pressures greater than 50–100 hPa).

Outdoor sports and risk of ultraviolet radiation-related skin lesions in children: evaluation of risks and prevention

Background  Excessive ultraviolet (UV) radiation exposure can cause skin cancers, skin photoageing and cataracts. Children are targeted by sun‐protection campaigns because high sun exposure and sunburn in childhood increase the risk of melanoma in adulthood. Little information is available about UV radiation risk and exposure in children who take part in outdoor sports.

Comparison of polar ozone loss rates simulated by one‐dimensional and three‐dimensional models with Match observations in recent Antarctic and Arctic winters

Simulations of ozone loss rates using a three-dimensional chemical transport model and a box model during recent Antarctic and Arctic winters are compared with experimental loss rates. The study focused on the Antarctic winter 2003, during which the first Antarctic Match campaign was organized, and on Arctic winters 1999/2000, 2002/2003. The maximum ozone loss rates retrieved by the Match technique for the winters and levels studied reached 6 ppbv/sunlit hour and both types of simulations could generally reproduce the observations at 2-sigma error bar level. In some cases, for example, for the Arctic winter 2002/2003 at 475 K level, an excellent agreement within 1-sigma standard deviation level was obtained. An overestimation was also found with the box model simulation at some isentropic levels for the Antarctic winter and the Arctic winter 1999/2000, indicating an overestimation of chlorine activation in the model. Loss rates in the Antarctic show signs of saturation in September, which have to be considered in the comparison. Sensitivity tests were performed with the box model in order to assess the impact of kinetic parameters of the ClO-Cl2O2 catalytic cycle and total bromine content on the ozone loss rate. These tests resulted in a maximum change in ozone loss rates of 1.2 ppbv/sunlit hour, generally in high solar zenith angle conditions. In some cases, a better agreement was achieved with fastest photolysis of Cl2O2 and additional source of total inorganic bromine but at the expense of overestimation of smaller ozone loss rates derived later in the winter.

Fine‐scale study of a thick stratospheric ozone lamina at the edge of the southern subtropical barrier

A large-scale transport event resulting in a thick ozone lamina originating from midlatitudes is observed in the tropical stratosphere over Reunion island (55°E, 21°S). This isentropic transport was detected from stratospheric balloon-borne ozone measurements that showed the occurrence of the lamina and was investigated using different tools based on Ertels potential vorticity (Epv) analyses. An original software (DYBAL) using surface coordinate and the equivalent length of Epv contours as diagnostic tools in conjunction with high-resolution outputs from an Epv advection model MIMOSA allows us to specify the origin of the lamina. The results indicate that a broad layer of stratospheric air was isentropically advected from midlatitudes across the southern edge of tropical reservoir and reached Reunion island on 12 July 2000. In addition, Eliassen-Palms flux vectors, calculated from ECMWF analysis, show that planetary wave activity was quite large during that time period, with wave-breaking occurring around 30 km, and could have driven that exchange. In contrast with analyses of filamentation events based on model and satellite data, the present study focuses on a fine-scale vertical survey from in situ measurements. The filament reported in this paper is characterized by a large vertical extension and is located around the maximum of ozone concentration in the tropical stratosphere (600 K). The analysis of such events, poorly documented in the tropics, could complement satellite studies and contribute to a better determination of the transport between the tropics and the midlatitudes.