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Assessment of quasi-global surface ozone simulations with WRF-chem using multi-dataset evaluation
Lingxia Wu1, Lei Li2, Lei Zhang2
1Key Laboratory for Aerosol-Cloud-Precipitation of China Meteorological Administration, Nanjing University of Information Science and Technology, Nanjing, 210044, China; State Key Laboratory of Severe Weather Meteorological Science and Technology & Key Laboratory of Atmospheric Chemistry of CMA, Chinese Academy of Meteorological Sciences, Beijing, 100081, China.
None:
This study performs a quasi-global surface ozone (O3) using the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem). The primary goal is to evaluate the O3 simulation performance of WRF-Chem. The model reproduced surface meteorology reasonably well, with the average correlation coefficients (R) and index of agreement (IOA) exceeding 0.7 when compared to ground-based observations from March 2019 to February 2020. The Tropospheric Ozone Assessment Report (TOAR) daily O3 observational data and two reanalysis datasets, CAMS and GEOS-CF hourly data, are used in this study to evaluate O3. WRF-Chem captured surface O3 variations in Europe when compared to TOAR data, with R greater than 0.6. Asia and Africa had an average R of 0.5 and a mean bias (MB) of -4.6 ppb, while the Americas did worse, with South America exhibiting an average overestimation of 11.2 ppb. The differences in nitric oxide (NO), nitrogen dioxide (NO2), and O3 between RADM2 and RACM are further examined. The largest NO2 differences occur over eastern China, northern India, and Europe, whereas the O3 differences are concentrated over tropical rainforest regions and the equatorial oceans, with mean absolute differences exceeding 10 ppb. Overall, the findings indicate that more advancements in model structure, chemical mechanisms, and meteorological parameters are still required to improve WRF-Chem's capacity to simulate quasi-global O3.
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