Ozone concentrations in excess of health‐based standards occur along the coastline of Lake Michigan. A complex pattern of ozone precursor emissions interfaces with a complex meteorological environment, presenting a challenge for air quality management and simulation. Precursors are transported into a shallow, stable boundary layer over the lake. This is followed by ozone formation and transport back onshore through a combination of synoptic and lake breeze winds. In this study, we use measurements during the Lake Michigan Ozone Study 2017 (LMOS) to quantitatively evaluate the Weather Research and Forecasting with Chemistry (WRF‐Chem) model at 4 km horizontal resolution for key features of high ozone episodes over Southern Lake Michigan, with a focus on meteorological performance. WRF‐Chem showed good performance and successful reproduction of meteorological fields and clouds. Lake breeze model skill was inconsistent, with both good and poor performance depending on site and day. The combination of Noah land surface model and High‐Resolution Rapid Refresh meteorology gave the best performance with the mean bias of −0.5 °C for temperature, −0.6 °C for dewpoint temperature, and −0.3 m/s for wind speed along the western coast of Lake Michigan during the daytime. For ozone, WRF‐Chem was biased low (−4.4 ppb mean bias for daytime ozone) and underestimated hourly peak ozone. In some cases, ozone bias can be attributed to transport and lake breeze errors. Average ozone concentration showed minor (<2 ppb) sensitivity to changes to meteorology initial and boundary conditions or the land surface model.
A new configuration of the Community Earth System Model (CESM)/Community Atmosphere Model with full chemistry (CAM-chem) supporting the capability of horizontal mesh refinement through the use of the spectral element (SE) dynamical core is developed and called CESM/CAM-chem-SE. Horizontal mesh refinement in CESM/CAM-chem-SE is unique and novel in that pollutants such as ozone are accurately represented at human exposure relevant scales while also directly including global feedbacks. CESM/ CAM-chem-SE with mesh refinement down to ∼14 km over the conterminous US (CONUS) is the beginning of the Multi-Scale Infrastructure for Chemistry and Aerosols (MUSICAv0). Here, MUSICAv0 is evaluated and used to better understand how horizontal resolution and chemical complexity impact ozone and ozone precursors over CONUS as compared to measurements from five aircraft campaigns, which occurred in 2013. This field campaign analysis demonstrates the importance of using finer horizontal resolution to accurately simulate ozone precursors such as nitrogen oxides and carbon monoxide. In general, the impact of using more complex chemistry on ozone and other oxidation products is more pronounced when using finer horizontal resolution where a larger number of chemical regimes are resolved. Large model biases for ozone near the surface remain in the Southeast US as compared to the aircraft observations even with updated chemistry and finer horizontal resolution. This suggests a need for adding the capability of replacing sections of global emission inventories with regional inventories, increasing the vertical resolution in the planetary boundary layer, and reducing model biases in meteorological variables such as temperature and clouds.Plain Language Summary A new configuration of the Community Earth System Model (CESM)/ Community Atmosphere Model with full chemistry (CAM-chem) supporting the capability of horizontal mesh refinement is developed. This configuration is the beginning of the Multi-Scale Infrastructure for Chemistry and Aerosols, which will create a unified infrastructure to model atmospheric chemistry and aerosols across scales in the Earth system. The capability in CESM/CAM-chem to use grids with horizontal mesh refinement SCHWANTES ET AL.
The Lake Michigan Ozone Study 2017 (LMOS 2017) was a collaborative multi-agency field study targeting ozone chemistry, meteorology, and air quality observations in the southern Lake Michigan area. The primary objective of LMOS 2017 was to provide measurements to improve air quality modeling of the complex meteorological and chemical environment in the region. LMOS 2017 science questions included spatiotemporal assessment of nitrogen oxides (NOx = NO + NO2) and volatile organic compounds (VOC) emission sources and their influence on ozone episodes, the role of lake breezes, contribution of new remote sensing tools such as GeoTASO, Pandora, and TEMPO to air quality management, and evaluation of photochemical grid models. The observing strategy included GeoTASO on board the NASA UC-12 capturing NO2 and formaldehyde columns, an in situ profiling aircraft, two ground-based coastal enhanced monitoring locations, continuous NO2 columns from coastal Pandora instruments, and an instrumented research vessel. Local photochemical ozone production was observed on 2 June, 9–12 June, and 14–16 June, providing insights on the processes relevant to state and federal air quality management. The LMOS 2017 aircraft mapped significant spatial and temporal variation of NO2 emissions as well as polluted layers with rapid ozone formation occurring in a shallow layer near the Lake Michigan surface. Meteorological characteristics of the lake breeze were observed in detail and measurements of ozone, NOx, nitric acid, hydrogen peroxide, VOC, oxygenated VOC (OVOC), and fine particulate matter (PM2.5) composition were conducted. This article summarizes the study design, directs readers to the campaign data repository, and presents a summary of findings.
Abstract. The Indo-Gangetic Plain (IGP) experienced an intensive air pollution episode during November 2017. Weather Research and Forecasting model coupled to Chemistry (WRF-Chem), a coupled meteorology–chemistry model, was used to simulate this episode. In order to capture PM2.5 peaks, we modified input chemical boundary conditions and biomass burning emissions. The Community Atmosphere Model with Chemistry (CAM-chem) and Modern-Era Retrospective analysis for Research and Applications Version 2 (MERRA-2) global models provided gaseous and aerosol chemical boundary conditions, respectively. We also incorporated Visible Infrared Imaging Radiometer Suite (VIIRS) active fire points to fill in missing fire emissions in the Fire INventory from NCAR (FINN) and scaled by a factor of 7 for an 8 d period. Evaluations against various observations indicated the model captured the temporal trend very well although missed the peaks on 7, 8, and 10 November. Modeled aerosol composition in Delhi showed secondary inorganic aerosols (SIAs) and secondary organic aerosols (SOAs) comprised 30 % and 27 % of total PM2.5 concentration, respectively, during November, with a modeled OC/BC ratio of 2.72. Back trajectories showed agricultural fires in Punjab were the major source for extremely polluted days in Delhi. Furthermore, high concentrations above the boundary layers in vertical profiles suggested either the plume rise in the model released the emissions too high or the model did not mix the smoke down fast enough. Results also showed long-range-transported dust did not affect Delhi's air quality during the episode. Spatial plots showed averaged aerosol optical depth (AOD) of 0.58 (±0.4) over November. The model AODs were biased high over central India and low over the eastern IGP, indicating improving emissions in the eastern IGP can significantly improve the air quality predictions. We also found high ozone concentrations over the domain, which indicates ozone should be considered in future air quality management strategies alongside particulate matter.
We develop an improved, wind‐driven lake spray aerosol (LSA) emissions parameterization that resolves particle size and size‐independent chemical composition, and investigate the impact of these emissions on regional chemistry in the Great Lakes region. We conduct Weather Research and Forecasting model with online Chemistry simulations for November 2015, a time period with high LSA emissions. LSA particles emitted from the surface of the Great Lakes increase particulate normalNnormalO3− by 37% over the Great Lakes and by 13% over land, primarily due to heterogeneous reactions between CaCO3 and HNO3. Cations emitted from lake spray affect the thermodynamic equilibrium, reducing particulate normalNnormalH4+ by 16% over the Great Lakes and by 7% over the surrounding land. This also influences gas‐phase species in the region, decreasing nitric acid by up to 32% over lakes. Overall, these simulations suggest that understanding LSA and its impact on other air pollutants is important for determining health and climate effects in the Great Lakes region.
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