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Central role of nitric oxide in ozone production in the upper tropical troposphere over the Atlantic Ocean and West Africa

MPG-Autoren
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Tadic,  Ivan
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Nussbaumer,  Clara
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Harder,  Hartwig
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Marno,  Daniel
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Martinez,  Monica
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Parchatka,  Uwe
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Pozzer,  Andrea
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Rohloff,  Roland
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Lelieveld,  Jos
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Fischer,  Horst
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Zitation

Tadic, I., Nussbaumer, C., Bohn, B., Harder, H., Marno, D., Martinez, M., et al. (2021). Central role of nitric oxide in ozone production in the upper tropical troposphere over the Atlantic Ocean and West Africa. Atmospheric Chemistry and Physics Discussions, 21. doi:10.5194/acp-2021-52.


Zitierlink: https://hdl.handle.net/21.11116/0000-0007-F30D-9
Zusammenfassung
Mechanisms of tropospheric ozone (O3) formation are generally well understood. However, studies reporting on net ozone production rates (NOPRs) directly derived from in-situ observations are challenging, and are sparse in number. To analyze the role of nitric oxide (NO) in net ozone production in the upper tropical troposphere above the Atlantic Ocean and the West African continent, we present in situ trace gas observations obtained during the CAFE-Africa (Chemistry of the Atmosphere: Field Experiment in Africa) campaign in August and September 2018. The vertical profile of in situ measured NO along the flight tracks reveals lowest NO mixing ratios of less than 20 pptv between 2 and 8 km altitude and highest mixing ratios of 0.15–0.2 ppbv above 12 km altitude. Spatial distribution of tropospheric NO above 12 km altitude shows that the sporadically enhanced local mixing ratios (> 0.4 ppbv) occur over the West African continent, which we attribute to episodic lightning events. Measured O3 shows little variability in mixing ratios at 60–70 ppbv, with slightly decreasing and increasing tendencies towards the boundary layer and stratosphere, respectively. Concurrent measurements of CO, CH4, OH and HO2 and H2O enable calculations of NOPRs along the flight tracks and reveal net ozone destruction at −0.6 to −0.2 ppbv h−1 below 6 km altitude and balance of production and destruction around 7–8 km altitude. We report vertical average NOPRs of 0.2–0.4 ppbv h−1 above 12 km altitude with NOPRs occasionally larger than 0.5 ppbv h−1 over West Africa coincident with enhanced NO. We compare the observational results to simulated data retrieved from the general circulation ECHAM/MESSy Atmospheric Chemistry (EMAC) model. Although the comparison of mean vertical profiles of NO and O3 indicates good agreement, local deviations between measured and modelled NO are substantial. The vertical tendencies in NOPRs calculated from simulated data largely reproduce those from in situ experimental data. However, the simulation results do not agree well with NOPRs over the West African continent. Both measurements and simulations indicate that ozone formation in the upper tropical troposphere is NOx-limited.