The influence of extratropical cross-tropopause mixing on the correlation between ozone and sulfate aerosol in the lowermost stratosphere
| Autor: | P. Joppe, J. Schneider, K. Kaiser, H. Fischer, P. Hoor, D. Kunkel, H.-C. Lachnitt, A. Marsing, L. Röder, H. Schlager, L. Tomsche, C. Voigt, A. Zahn, S. Borrmann |
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| Jazyk: | angličtina |
| Rok vydání: | 2024 |
| Předmět: | |
| Zdroj: | Atmospheric Chemistry and Physics, Vol 24, Pp 7499-7522 (2024) |
| Druh dokumentu: | article |
| ISSN: | 1680-7316 1680-7324 |
| DOI: | 10.5194/acp-24-7499-2024 |
| Popis: | The chemical composition of the upper troposphere/lower stratosphere region (UTLS) is influenced by horizontal transport of air masses, vertical transport within convective systems and warm conveyor belts, rapid turbulent mixing, as well as photochemical production or loss of species. This results in the formation of the extratropical transition layer (ExTL), which is defined by the vertical structure of CO and has been studied until now mostly by means of trace gas correlations. Here, we extend the analysis to include aerosol particles and derive the sulfate–ozone correlation in central Europe from aircraft in situ measurements during the CAFE-EU (Chemistry of the Atmosphere Field Experiment over Europe)/BLUESKY mission. The mission probed the UTLS during the COVID-19 period with significantly reduced anthropogenic emissions. We operated a compact time-of-flight aerosol mass spectrometer (C-ToF-AMS) to measure the chemical composition of non-refractory aerosol particles in the size range from about 40 to 800 nm. In our study, we find a correlation between the sulfate mass concentration and O3 in the lower stratosphere. The correlation exhibits some variability exceeding the mean sulfate–ozone correlation over the measurement period. Especially during one flight, we observed enhanced mixing ratios of sulfate aerosol in the lowermost stratosphere, where the analysis of trace gases shows tropospheric influence. However, back trajectories indicate that no recent mixing with tropospheric air occurred within the last 10 d. Therefore, we analyzed volcanic eruption databases and satellite SO2 retrievals from the TROPOspheric Monitoring Instrument (TROPOMI) for possible volcanic plumes and eruptions to explain the high amounts of sulfur compounds in the UTLS. From these analyses and the combination of precursor and particle measurements, we conclude that gas-to-particle conversion of volcanic SO2 leads to the observed enhanced sulfate aerosol mixing ratios. |
| Databáze: | Directory of Open Access Journals |
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