Tropospheric ozone simulated by a global-multi-regional two-way coupling model system

Abstract:

Current global chemical transport models are limited by horizontal resolutions (100-500 km), and they cannot capture small-scale processes affecting tropospheric ozone (O₃). Here we use a recently built two-way coupling system of GEOS-Chem to simulate the global tropospheric O₃ in 2009. The system couples the global model (~ 200 km) and its three nested models (~ 50 km) covering Asia, North America and Europe, respectively. Benefiting from the high resolution, the nested models better capture small-scale processes than the global model alone. In the coupling system, the nested models provide results to modify the global model simulation within respective nested domains while taking the lateral boundary conditions from the global model.

Due to the "coupling" effects, the two-way system significantly improves the tropospheric O₃ simulation upon the global model alone, as found by comparisons with a suite of ground (1420 sites from WDCGG, GMD, EMEP, and AQS), aircraft (HIPPO and MOZAIC), and satellite measurements (two OMI products). Compared to the global model alone, the two-way coupled simulation enhances the correlation in day-to-day variation of afternoon mean O₃ with the ground measurements from 0.53 to 0.68 and reduces the mean model bias from 10.8 to 6.7 ppb. Regionally, the coupled model reduces the bias by 4.6 ppb over Europe, 3.9 ppb over North America, and 3.1 ppb over other regions. The two-way coupling brings O₃ vertical profiles much closer to the HIPPO and MOZAIC data, reducing the tropospheric (0–9 km) mean bias by 3–10 ppb at most MOZAIC sites and by 5.3 ppb for HIPPO profiles. The two-way coupled simulation also reduces the global tropospheric column ozone by 3.0 DU (9.5%), bringing them closer to the OMI data in all seasons. Simulation improvements are more significant in the northern hemisphere, and are primarily a result of improved representation of the nonlinear ozone chemistry, including but not limited to urban-rural contrast.

The two-way coupled simulation also reduces the global tropospheric mean hydroxyl radical by 5% with enhancements by 5% in lifetimes of methyl chloroform and methane, bringing them closer to observation-based estimates. Therefore improving model representations of small-scale processes are a critical step forward to understanding the global tropospheric chemistry.