In support of the first Tropospheric Ozone Assessment Report (TOAR) a relational database of global surface ozone observations has been developed and populated with hourly measurement data and enhanced metadata. A comprehensive suite of ozone data products including standard statistics, health and vegetation impact metrics, and trend information, are made available through a common data portal and a web interface. These data form the basis of the TOAR analyses focusing on human health, vegetation, and climate relevant ozone issues, which are part of this special feature. Cooperation among many data centers and individual researchers worldwide made it possible to build the world’s largest collection of in-situ hourly surface ozone data covering the period from 1970 to 2015. By combining the data from almost 10,000 measurement sites around the world with global metadata information, new analyses of surface ozone have become possible, such as the first globally consistent characterisations of measurement sites as either urban or rural/remote. Exploitation of these global metadata allows for new insights into the global distribution, and seasonal and long-term changes of tropospheric ozone and they enable TOAR to perform the first, globally consistent analysis of present-day ozone concentrations and recent ozone changes with relevance to health, agriculture, and climate. Considerable effort was made to harmonize and synthesize data formats and metadata information from various networks and individual data submissions. Extensive quality control was applied to identify questionable and erroneous data, including changes in apparent instrument offsets or calibrations. Such data were excluded from TOAR data products. Limitations of a posteriori data quality assurance are discussed. As a result of the work presented here, global coverage of surface ozone data for scientific analysis has been significantly extended. Yet, large gaps remain in the surface observation network both in terms of regions without monitoring, and in terms of regions that have monitoring programs but no public access to the data archive. Therefore future improvements to the database will require not only improved data harmonization, but also expanded data sharing and increased monitoring in data-sparse regions.
1 May 2018 in Bulletin of the American Meteorological Society
We describe and show results from a series of field campaigns that used balloonborne instruments launched from India and Saudi Arabia during the summers 2014–17 to study the nature, formation, and impacts of the Asian Tropopause Aerosol Layer (ATAL). The campaign goals were to i) characterize the optical, physical, and chemical properties of the ATAL; ii) assess its impacts on water vapor and ozone; and iii) understand the role of convection in its formation. To address these objectives, we launched 68 balloons from four locations, one in Saudi Arabia and three in India, with payload weights ranging from 1.5 to 50 kg. We measured meteorological parameters; ozone; water vapor; and aerosol backscatter, concentration, volatility, and composition in the upper troposphere and lower stratosphere (UTLS) region. We found peaks in aerosol concentrations of up to 25 cm–3 for radii > 94 nm, associated with a scattering ratio at 940 nm of ∼1.9 near the cold-point tropopause. During medium-duration balloon flights near the tropopause, we collected aerosols and found, after offline ion chromatography analysis, the dominant presence of nitrate ions with a concentration of about 100 ng m–3. Deep convection was found to influence aerosol loadings 1 km above the cold-point tropopause. The Balloon Measurements of the Asian Tropopause Aerosol Layer (BATAL) project will continue for the next 3–4 years, and the results gathered will be used to formulate a future National Aeronautics and Space Administration–Indian Space Research Organisation (NASA–ISRO) airborne campaign with NASA high-altitude aircraft.
15 August 2006 in Journal of Geophysical Research: Atmospheres
Absorbing aerosols supplements the global warming caused by greenhouse gases. However, unlike greenhouse gases, the effect of absorbing aerosol on climate is not known with certainty owing to paucity of data. Also, uncertainty exists in quantifying the contributing factors whether it is biomass or fossil fuel burning. Based on the observations of absorption coefficient at seven wavelengths and aerosol optical depth (AOD) at five wavelengths carried out at Gadanki (13.5° N, 79.2° E), a remote village in peninsular India, from April to November 2008, as part of the "Study of Atmospheric Forcing and Responses (SAFAR)" pilot campaign we discuss seasonal variation of black carbon (BC) concentration and aerosol optical depth. Also, using spectral information we estimate the fraction of fossil-fuel and non-fossil fuel contributions to absorption coefficient and contributions of soot (Black Carbon), non-soot fine mode aerosols and coarse mode aerosols to AOD. BC concentration is found to be around 1000 ng/m3 during monsoon months (JJAS) and around 4000 ng/m3 during pre and post monsoon months. Non-fossil fuel sources contribute nearly 20% to absorption coefficient at 880 nm, which increases to 40% during morning and evening hours. Average AOD is found to be 0.38±0.15, with high values in May and low in September. Soot contributes nearly 10% to the AOD. This information is further used to estimate the clear sky aerosol direct radiative forcing. Top of the atmosphere aerosol radiative forcing varies between −4 to 0 W m−2, except for April when the forcing is positive. Surface level radiative forcing is between −10 to −20 W m−2. The net radiation absorbed within the atmosphere is in the range of 9 to 25 W m−2, of which soot contributes about 80 to 90%.
22 December 2006 in Journal of Geophysical Research: Atmospheres