Influence of stratospheric airmasses on tropospheric vertical O₃ columns based on GOME (Global Ozone Monitoring Experiment) measurements and backtrajectory calculation over the Pacific

Satellite based GOME (Global Ozone Measuring experiment) data are used to characterize the amount of tropospheric ozone over the tropical Pacific. Tropospheric ozone was determined from GOME data using the Tropospheric Excess Method (TEM). In the tropical Pacific a significant seasonal variation is detected. Tropospheric excess ozone is enhanced during the biomass burning season from September to November due to outflow from the continents. In September 1999 GOME data reveal an episode of increased excess ozone columns over Tahiti (18.0° S; 149.0° W) (Eastern Pacific) compared to Am. Samoa (14.23° S; 170.56° W) and Fiji (18.13° S; 178.40° E), both situated in the Western Pacific. Backtrajectory calculations show that none of the airmasses arriving over the three locations experienced anthropogenic pollution (e. g. biomass burning). Consequently other sources of ozone have to be considered. One possible process leading to an increase of tropospheric ozone is stratosphere-troposphere-exchange. An analysis of the potential vorticity along trajectories arriving above each of the locations reveals that airmasses at Tahiti are subject to enhanced stratospheric influence, compared to Am. Samoa and Fiji. As a result this study shows clear incidents of transport of airmasses from the stratosphere into the troposphere

Tropospheric O₃ over Indonesia during biomass burning events measured with GOME (Global Ozone Monitoring Experiment) and compared with trajectory analysis

International audienceTropospheric ozone columns of up to 50 DU were observed by GOME (Global Ozone Monitoring Experiment) above Indonesia in September 1997, while only background amounts were measured in September 1998. The Traj.x trajectory model along with BRemen's Atmospheric PHOtochemical model (BRAPHO) were used to investigate the higher than average ozone columns above Indonesia. The transport analysis reveals that biomass burning over central Africa and northern Australia does not significantly influence ozone columns over Indonesia in September 1997. El Niño conditions, leading to extreme dryness and uncontrolled fires in Indonesia, produced ozone precursors, which are initially only slowly advected westwards to the central Indian Ocean. Joint transport and chemistry modelling was able to reproduce the spatial distribution and amounts of ozone, NO2 and formaldehyde columns over Indonesia. The chemistry modelling shows a net production of 3.1 Tg of ozone produced by biomass burning in Indonesia in September 1997. Transport analysis further reveals that ozone columns over the Indian Ocean, between 10 and 20° S can be accounted for by the mixing of air masses containing NOx from lightning over the Congo Basin with air masses containing volatile organic compounds from biomass burning

Transport and build-up of tropospheric trace gases during the MINOS campaign: comparision of GOME, in situ aircraft measurements and MATCH-MPIC-data

The MINOS (Mediterranean INtensive Oxidant Study) campaign was an international, multi-platform field campaign to measure long-range transport of air-pollution and aerosols from South East Asia and Europe towards the Mediterranean basin during August 2001. High pollution events were observed during this campaign. For the Mediterranean region enhanced tropospheric nitrogen dioxide (NO₂) and formaldehyde (HCHO), which are precursors of tropospheric ozone (O₃), were detected by the satellite based GOME (Global Ozone Monitoring Experiment) instrument and compared with airborne in situ measurements as well as with the output from the global 3D photochemistry-transport model MATCH-MPIC (Model of Atmospheric Transport and CHemistry - Max Planck Institute for Chemistry). The increase of pollution in that region leads to severe air quality degradation with regional and global implications

Space-based formaldehyde measurements as constrains on volatile organic compound emissions in east and south Asia and implications for ozone

We use a continuous 6-year record (1996–2001) of GOME satellite measurements of formaldehyde (HCHO) columns over east and south Asia to improve regional emission estimates of reactive nonmethane volatile organic compounds (NMVOCs), including isoprene, alkenes, HCHO, and xylenes. Mean monthly HCHO observations are compared to simulated HCHO columns from the GEOS-Chem chemical transport model using state-of-science, “bottom-up” emission inventories from Streets et al. (2003a) for anthropogenic and biomass burning emissions and Guenther et al. (2006) for biogenic emissions (MEGAN). We find that wintertime GOME observations can diagnose anthropogenic reactive NMVOC emissions from China, leading to an estimate 25% higher than Streets et al. (2003a). We attribute the difference to vehicular emissions. The biomass burning source for east and south Asia is almost 5 times the estimate of Streets et al. (2003a). GOME reveals a large source from agricultural burning in the North China Plain in June missing from current inventories. This source may reflect a recent trend toward in-field burning of crop residues as the need for biofuels diminishes. Biogenic isoprene emission in east and south Asia derived from GOME is 56 ± 30 Tg yr−1, similar to 52 Tg yr−1 from MEGAN. We find, however, that MEGAN underestimates emissions in China and overestimates emissions in the tropics. The higher Chinese biogenic and biomass burning emissions revealed by GOME have important implications for ozone pollution. We find 5 to 20 ppb seasonal increases in surface ozone in GEOS-Chem for central and northern China when using GOME-derived versus bottom-up emissions. Our methodology can be adapted for other regions of the world to provide top-down constraints on NMVOC emissions where multiple emission source types overlap in space and time.Earth and Planetary SciencesEngineering and Applied Science

Peroxy radical observations over West Africa during AMMA 2006: photochemical activity in the outflow of convective systems

Peroxy radical measurements made on board the DLR-Falcon research aircraft over West Africa within the African Monsoon Multidisciplinary Analysis (AMMA) campaign during the 2006 wet monsoon are presented in this study. The analysis of data focuses on the photochemical activity of air masses sampled during episodes of intense convection and biomass burning. Generally, the total sum of peroxy radical mixing ratios, measured in the outflow of convective clouds, are quite variable but occasionally are coupled with the NO variations indicating the coexistence or simultaneous emission of NOx, with a potential radical precursor (i.e. formaldehyde, acetone or peroxides), which has likely been transported to higher atmospheric altitudes. Based on the measurements, significant O3 production rates around 1 ppb/h in the MCS outflow are estimated by using a box model with simplified chemistry. Peroxy radicals having mixing ratios around 20�25 pptv and with peak values of up to 60�70 pptv are measured within biomass burning plumes, detected at the coast in Ghana. Calculations of back-trajectory densities confirm the origin of these air masses being a biomass burning region at southern latitudes and close to the Gulf of Guinea, according to satellite pictures. Measured peroxy radical concentrations agree reasonably with modelled estimations taking into account simple local chemistry. Moreover, the vertical profiles taken at the aircraft base in Ouagadougou, Burkina Faso, indicate the common feature of having maximum concentrations between 2 and 4 km, in agreement with other literature values obtained under similar conditions