Natural and anthropogenic influence on tropospheric ozone variability over the Tropical Atlantic unveiled by satellite, reanalyses and in situ observations

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Abstract

Tropospheric ozone over the South and Tropical Atlantic plays an important role in the photochemistry and energy budget of the atmosphere. In this remote region, tropospheric ozone estimates from reanalysis datasets show the largest discrepancies. The present study characterises the vertical and horizontal distribution of tropospheric ozone over the South and Tropical Atlantic during February and October 2017 using a multispectral synergism called IASI + GOME2, two global chemistry reanalysis products - the Copernicus Atmosphere Monitoring Service reanalysis (CAMS reanalysis) and the Tropospheric Chemistry Reanalysis version 2 (TCR-2) - and in situ airborne measurements from the Atmospheric Tomography Mission (ATom). In February, biomass burning in West and Central Africa and deep convection over the Gulf of Guinea strongly influence the region. IASI + GOME2 captures enhanced ozone abundances in the Southern Hemisphere and low ozone concentrations in the Northern Hemisphere, exhibiting excellent agreement with ATom-2 profiles. In contrast, both reanalyses underestimate lower-tropospheric ozone influenced by biomass-burning outflow and overestimate ozone in the Northern Hemisphere due to excessive contributions from stratospheric intrusion and North American anthropogenic emissions. In October, tropospheric ozone enhancement associated with biomass-burning outflow from Austral Africa is consistently depicted by observations and reanalyses. These results emphasize the need to evaluate the seasonal variability of each of the multiple sources of ozone precursors within atmospheric chemistry reanalyses.

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Okamoto, S., Cuesta, J., Dufour, G., Eremenko, M., Miyazaki, K., Boonne, C., … Thompson, C. (2026). Natural and anthropogenic influence on tropospheric ozone variability over the Tropical Atlantic unveiled by satellite, reanalyses and in situ observations. Atmospheric Chemistry and Physics, 26(7), 4685–4709. https://doi.org/10.5194/acp-26-4685-2026

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