Evaluating tropospheric nitrogen dioxide in UKCA using OMI satellite retrievals over south and east Asia

Abstract. We compare tropospheric column nitrogen dioxide (NO2) in the United Kingdom Chemistry and Aerosol (UKCA) model version 11.0 with satellite measurements from NASA's Earth Observing System (EOS) Aura satellite Ozone Monitoring Instrument (OMI) to investigate the seasonality and trends of tropospheric NO2 over south and east Asia (S and E Asia). UKCA is the atmospheric composition component of the UK Earth System Model (UKESM). UKCA was run with nudged meteorology, producing hourly output over S and E Asia for 2005–2015. OMI averaging kernels have been applied to the model hourly data sampled at Aura's local overpass time of 13:45 LT ± 15 min to allow for consistent model–data comparison. Background UKCA and OMI tropospheric column NO2 typically ranges between 0×1015 and 2×1015 molec.cm-2. Diurnal cycles and vertical profiles of the tropospheric NO2 column in UKCA show that the daily minimum tropospheric column NO2 occurs around the satellite overpass time. UKCA captures the seasonality but overestimates NO2 by a factor of ∼ 2.5, especially during winter over eastern China and north India, at times and locations with high aerosol loadings. Heterogeneous chemistry is represented in the version of UKCA used here as uptake of N2O5 on internally generated sulfate aerosol. However, aerosol surface area may be underestimated in polluted locations, contributing to overestimation of NO2. In addition, the model may underestimate emissions of volatile organic compounds (VOCs) and associated peroxy acetyl nitrate (PAN) formation, leading to insufficient long-range transport of oxidised nitrogen and also contributing to overestimation of NO2 over polluted regions and underestimation over remote regions. Quantifying and understanding discrepancies in modelled NO2 warrant further investigation as they propagate into modelling of multiple environmental issues.

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Journal
Atmospheric chemistry and physics
Published
2025-05-08
DOI
https://doi.org/10.5194/acp-25-4785-2025
Primary Topic
Atmospheric Ozone and Climate
Type
article
Field-Weighted Citation Impact
0.00

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Evaluating tropospheric nitrogen dioxide in UKCA using OMI satellite retrievals over south and east Asia

Ryan Hossaini, David S. Stevenson, Alcide Zhao, Richard Pope et al.
Atmospheric chemistry and physics
Atmospheric Ozone and Climate
article

Evaluating tropospheric nitrogen dioxide in UKCA using OMI satellite retrievals over south and east Asia

Ryan Hossaini, David S. Stevenson, Alcide Zhao, Richard Pope, Alok Kumar Pandey, Martyn P. Chipperfield, Krishan Kumar
article en

Abstract

Abstract. We compare tropospheric column nitrogen dioxide (NO2) in the United Kingdom Chemistry and Aerosol (UKCA) model version 11.0 with satellite measurements from NASA's Earth Observing System (EOS) Aura satellite Ozone Monitoring Instrument (OMI) to investigate the seasonality and trends of tropospheric NO2 over south and east Asia (S and E Asia). UKCA is the atmospheric composition component of the UK Earth System Model (UKESM). UKCA was run with nudged meteorology, producing hourly output over S and E Asia for 2005–2015. OMI averaging kernels have been applied to the model hourly data sampled at Aura's local overpass time of 13:45 LT ± 15 min to allow for consistent model–data comparison. Background UKCA and OMI tropospheric column NO2 typically ranges between 0×1015 and 2×1015 molec.cm-2. Diurnal cycles and vertical profiles of the tropospheric NO2 column in UKCA show that the daily minimum tropospheric column NO2 occurs around the satellite overpass time. UKCA captures the seasonality but overestimates NO2 by a factor of ∼ 2.5, especially during winter over eastern China and north India, at times and locations with high aerosol loadings. Heterogeneous chemistry is represented in the version of UKCA used here as uptake of N2O5 on internally generated sulfate aerosol. However, aerosol surface area may be underestimated in polluted locations, contributing to overestimation of NO2. In addition, the model may underestimate emissions of volatile organic compounds (VOCs) and associated peroxy acetyl nitrate (PAN) formation, leading to insufficient long-range transport of oxidised nitrogen and also contributing to overestimation of NO2 over polluted regions and underestimation over remote regions. Quantifying and understanding discrepancies in modelled NO2 warrant further investigation as they propagate into modelling of multiple environmental issues.

Atmospheric chemistry and physicsVol. 25(9)
University of Delhi (IN), University of Leeds (GB), Jawaharlal Nehru University (IN), National Centre for Earth Observation (GB), Lancaster University (GB), University of Edinburgh (GB)
Global Challenges Research Fund, Commonwealth Scholarship Commission, National Centre for Earth Observation
Openalex Percentile: Top 86%
Atmospheric Ozone and Climate
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