Daily ozonesondes were launched from 14 North American sites during August 2006, providing the best set of free tropospheric ozone measurements ever gathered across the continent in a single season. The data reveal a distinct upper tropospheric ozone maximum above eastern North America and centered over the southeastern USA. Recurring each year, the location and strength of the ozone maximum is influenced by the summertime upper tropospheric anticyclone that traps convectively lofted ozone, ozone precursors and lightning NOx above the southeastern USA. The North American summer monsoon that flows northward along the Rocky Mountains is embedded within the western side of the anticyclone and also marks the westernmost extent of the ozone maximum. Removing the influence from stratospheric intrusions, median ozone mixing ratios (78 ppbv) in the upper troposphere (>6 km) above Alabama, near the center of the anticyclone, were nearly twice the level above the U.S. west coast. Simulations by an atmospheric chemistry general circulation model indicate lightning NOx emissions led to the production of 25–30 ppbv of ozone at 250 hPa above the southern United States during the study period. On the regional scale the ozone enhancement above the southeastern United States produced a positive all‐sky adjusted radiative forcing up to 0.50 W m−2.

International audienceThe Concordiasi project is making innovative observations of the atmosphere above Antarctica. The most important goals of the Concordiasi are as follows: 1. To enhance the accuracy of weather prediction and climate records in Antarctica through the assimilation of in situ and satellite data, with an emphasis on data provided by hyperspectral infrared sounders. The focus is on clouds, precipitation, and the mass budget of the ice sheets. The improvements in dynamical model analyses and forecasts will be used in chemical-transport models that describe the links between the polar vortex dynamics and ozone depletion, and to advance the understanding of the Earth system by examining the interactions between Antarctica and lower latitudes. 2. To improve our understanding of microphysical and dynamical processes controlling the polar ozone, by providing the first quasi-Lagrangian observations of stratospheric ozone and particles, in addition to an improved characterization of the 3D polar vortex dynamics. Techniques for assimilating these Lagrangian observations are being developed. A major Concordiasi component is a field experiment during the austral springs of 2008-10. The field activities in 2010 are based on a constellation of up to 18 long-duration stratospheric super-pressure balloons (SPBs) deployed from the McMurdo station. Six of these balloons will carry GPS receivers and in situ instruments measuring temperature, pressure, ozone, and particles. Twelve of the balloons will release drop-sondes on demand for measuring atmospheric parameters. Lastly, radiosounding measurements are collected at various sites, including the Concordia station

Abstract. Understanding the sources and evolution of aerosols is crucial for constraining the impacts that aerosols have on a global scale. An unanswered question in atmospheric science is the source and evolution of the Antarctic aerosol population. Previous work over the continent has primarily utilized low temporal resolution aerosol filters to answer questions about the chemical composition of Antarctic aerosols. Bulk aerosol sampling has been useful in identifying seasonal cycles in the aerosol populations, especially in populations that have been attributed to Southern Ocean phytoplankton emissions. However, real-time, high-resolution chemical composition data are necessary to identify the mechanisms and exact timing of changes in the Antarctic aerosol. The recent 2ODIAC (2-Season Ozone Depletion and Interaction with Aerosols Campaign) field campaign saw the first ever deployment of a real-time, high-resolution aerosol mass spectrometer (SP-AMS – soot particle aerosol mass spectrometer – or AMS) to the continent. Data obtained from the AMS, and a suite of other aerosol, gas-phase, and meteorological instruments, are presented here. In particular, this paper focuses on the aerosol population over coastal Antarctica and the evolution of that population in austral spring. Results indicate that there exists a sulfate mode in Antarctica that is externally mixed with a mass mode vacuum aerodynamic diameter of 250 nm. Springtime increases in sulfate aerosol are observed and attributed to biogenic sources, in agreement with previous research identifying phytoplankton activity as the source of the aerosol. Furthermore, the total Antarctic aerosol population is shown to undergo three distinct phases during the winter to summer transition. The first phase is dominated by highly aged sulfate particles comprising the majority of the aerosol mass at low wind speed. The second phase, previously unidentified, is the generation of a sub-250 nm aerosol population of unknown composition. The second phase appears as a transitional phase during the extended polar sunrise. The third phase is marked by an increased importance of biogenically derived sulfate to the total aerosol population (photolysis of dimethyl sulfate and methanesulfonic acid (DMS and MSA)). The increased importance of MSA is identified both through the direct, real-time measurement of aerosol MSA and through the use of positive matrix factorization on the sulfur-containing ions in the high-resolution mass-spectral data. Given the importance of sub-250 nm particles, the aforementioned second phase suggests that early austral spring is the season where new particle formation mechanisms are likely to have the largest contribution to the aerosol population in Antarctica.

Enhancements in ozone were observed between about 3 and 10 km altitude within an electrically active storm in central New Mexico. Measurements from satellite sensors and ground‐based radar show cloud top pressures between 300 and 150 mb in the vicinity of an ozonesonde launched from Socorro, NM, and heavy precipitation with radar reflectivities exceeding 50 dBZ. Data from a lightning mapping array and a surface electric field mill show a large amount of electrical activity within this thunderstorm. The observed ozone enhancements are large (50% above the mean) and could have resulted from a number of possible processes, including the advection of polluted air from the urban environments of El Paso and Juarez, photochemical production by lightning‐generated NOx from aged thunderstorm outflow, downward mixing of stratospheric air, or local production from within the thunderstorm. We find that a large fraction of the ozone enhancement is consistent with local production from corona discharges, either from cloud particles or by corona associated with lightning. The implied global source of ozone from thunderstorm corona discharge is estimated to be 110 Tg O3 a−1 with a range between 40 and 180 Tg O3 a−1. This value is about 21% as large as the estimated ozone production rate from lightning NOx, and about 3% as large as the total chemical production rate of tropospheric ozone. Thus while the estimated corona‐induced production of ozone may be significant on local scales, it is unlikely to be as important to the global ozone budget as other sources.