Improved characterization of the spatiotemporal extent, intensity, and causes of extreme aerosol optical depth events is critical to quantifying their regional climate forcing and the link to near‐surface air quality. An analysis of regional‐scale extreme aerosol events over the eastern United States is undertaken using output from the Modern‐Era Retrospective analysis for Research and Applications, version 2 (MERRA‐2) reanalysis and observations from the MODerate resolution Imaging Spectroradiometers (MODIS). Six extreme aerosol optical depth (AOD) events during 2003–2007, dominated by anthropogenic emissions and characterized by a regional scale extent, are identified and simulated using the Weather Research and Forecasting model coupled with Chemistry (WRF‐Chem) applied at 12 km resolution. Statistical analyses show output from WRF‐Chem during these events is generally negatively biased in terms of the mean AOD and PM2.5, but WRF‐Chem exhibits skill in capturing the peak AOD. WRF‐Chem also exhibits fidelity in reproducing the spatiotemporal characteristics of the extreme AOD events in intensity, location of centroid, propagation, duration, and their spatial extension. Considerable event‐to‐event variability in model skill in simulating spatial patterns of extreme events is observed, with the highest spatial correlation with MERRA‐2 AOD noted for events centered in the Midwest. Mean fractional bias in modeled peak AOD is minimized for the most intense events and for events centered over the southeastern USA. WRF‐Chem output is also negatively biased in downwelling shortwave radiation at the ground and specific humidity consistent with a positive bias in simulated precipitation relative to MERRA‐2.
This paper examines the accuracy of Weather Research and Forecasting model coupled with Chemistry (WRF‐Chem) generated 72 hr fine particulate matter (PM2.5) forecasts in Delhi during the crop residue burning season of October‐November 2017 with respect to assimilation of the Moderate Resolution Imaging Spectroradiometer (MODIS) aerosol optical depth (AOD) retrievals, persistent fire emission assumption, and aerosol‐radiation interactions. The assimilation significantly pushes the model AOD and PM2.5toward the observations with the largest changes below 5 km altitude in the fire source regions (northeastern Pakistan, Punjab, and Haryana) as well as the receptor New Delhi. WRF‐Chem forecast with MODIS AOD assimilation, aerosol‐radiation feedback turned on, and real‐time fire emissions reduce the mean bias by 88–195 μg/m3(70–86%) with the largest improvement during the peak air pollution episode of 6–13 November 2017. Aerosol‐radiation feedback contributes ~21%, ~25%, and ~24% to reduction in mean bias of the first, second, and third days of PM2.5forecast. Persistence fire emission assumption is found to work really well, as the accuracy of PM2.5forecasts driven by persistent fire emissions was only 6% lower compared to those driven by real fire emissions. Aerosol‐radiation feedback extends the benefits of assimilating satellite AOD beyond PM2.5forecasts to surface temperature forecast with a reduction in the mean bias of 0.9–1.5°C (17–30%). These results demonstrate that air quality forecasting can benefit substantially from satellite AOD observations particularly in developing countries that lack resources to rapidly build dense air quality monitoring networks.
more » « less- NSF-PAR ID:
- 10379072
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Journal of Geophysical Research: Atmospheres
- Volume:
- 125
- Issue:
- 17
- ISSN:
- 2169-897X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
Abstract -
Abstract Long‐range aerosol transport is an important physical mechanism for ecological, biological, and hydrological elements of the earth system. Regarding the latter, regional climate models have no way of assimilating future aerosol concentrations, so dust aerosol emissions must be parameterized using local landscape and meteorological conditions. The purpose of this study is to evaluate the accuracy of different dust emission settings within the Weather Research and Forecasting model coupled with chemistry (WRF‐Chem) to facilitate future dynamical downscaling work. This study performs nine WRF‐Chem hindcasts, each utilizing a different dust emission configuration, from 1 March to 31 May 2015, coinciding with a Saharan air layer (SAL) dust outbreak during the 2015 Caribbean drought. WRF‐Chem aerosol optical depth (AOD) and Gálvez‐Davison Index (GDI), a convective forecasting parameter, are validated against analogous MODIS, AERONET, and ERA5 products. In aggregate, the GOCART dust emission scheme with Air Force Weather Agency modifications (GOCART‐AFWA) achieved the best balance between AOD and GDI accuracy when employing the default tuning constant (1.00). As the schemes emitted dust more aggressively, WRF‐Chem produced warming at 500 hPa, reducing GDI over the central and eastern Atlantic near the modeled dust trajectory. Though AOD was generally too low over the southwest Atlantic, the eastern Caribbean occupies a transition zone between negative and positive AOD biases where this field was hindcast with relative accuracy. Meanwhile, areas with positive AOD biases were associated with negative GDI biases (and vice versa) indicating the covariability between SAL dust loadings and thermodynamic conditions in the tropical north Atlantic.
-
Abstract This study introduces a new chemistry option in the Weather Research and Forecasting model data assimilation (WRFDA) system, coupled with the WRF‐Chem model (Version 4.4.1), to incorporate aqueous chemistry (AQCHEM) in the assimilation of ground‐level chemical measurements. The new DA capability includes the integration of aqueous‐phase aerosols from the Regional Atmospheric Chemistry Mechanism (RACM) gas chemistry, the Modal Aerosol Dynamics Model for Europe (MADE) aerosol chemistry, and the Volatility Basis Set (VBS) for secondary organic aerosol production. The RACM‐MADE‐VBS‐AQCHEM scheme facilitates aerosol‐cloud‐precipitation interactions by activating aerosol particles in cloud water during the model simulation. With the goal of enhancing air quality forecasting in cloudy conditions, this new implementation is demonstrated in the weakly coupled three‐dimensional variational data assimilation (3D‐Var) system through regional air quality cycling over East Asia. Surface particulate matter (PM) concentrations and four gas species (SO2, NO2, O3, and CO) are assimilated every 6 hr for the month of March 2019. The results show that including aqueous‐phase aerosols in both the analysis and forecast can represent aerosol wet removal processes associated with cloud development and rainfall production. During a pollution event with high cloud cover, simulations without aerosols defined in cloud water exhibit significantly higher values for liquid water path, and surface PM10(PM2.5) concentrations are overestimated by a factor of 10 (3) when wet scavenging processes dominate. On the contrary, AQCHEM proves to be helpful in simulating the wet deposition of aerosols, accurately predicting the evolution of surface PM concentrations without such overestimation.
-
Abstract This study evaluates the impact of assimilating moderate resolution imaging spectroradiometer (MODIS) aerosol optical depth (AOD) data using different data assimilation (DA) methods on dust analyses and forecasts over North Africa and tropical North Atlantic. To do so, seven experiments are conducted using the Weather Research and Forecasting dust model and the Gridpoint Statistical Interpolation analysis system. Six of these experiments differ in whether or not AOD observations are assimilated and the DA method used, the latter of which includes the three‐dimensional variational (3D‐Var), ensemble square root filter (EnSRF), and hybrid methods. The seventh experiment, which allows us to assess the impact of assimilating deep blue AOD data, assimilates only dark target AOD data using the hybrid method. The assimilation of MODIS AOD data clearly improves AOD analyses and forecasts up to 48 hr in length. Results also show that assimilating deep blue data has a primarily positive effect on AOD analyses and forecasts over and downstream of the major North African source regions. Without assimilating deep blue data (assimilating dark target only), AOD assimilation only improves AOD forecasts for up to 30 hr. Of the three DA methods examined, the hybrid and EnSRF methods produce better AOD analyses and forecasts than the 3D‐Var method does. Despite the clear benefit of AOD assimilation for AOD analyses and forecasts, the lack of information regarding the vertical distribution of aerosols in AOD data means that AOD assimilation has very little positive effect on analyzed or forecasted vertical profiles of backscatter.
-
Abstract Since 2013, Chinese policies have dramatically reduced emissions of particulates and their gas‐phase precursors, but the implications of these reductions for aerosol‐radiation interactions are unknown. Using a global, coupled chemistry‐climate model, we examine how the radiative impacts of Chinese air pollution in the winter months of 2012 and 2013 affect local meteorology and how these changes may, in turn, influence surface concentrations of PM2.5, particulate matter with diameter <2.5 μm. We then investigate how decreasing emissions through 2016 and 2017 alter this impact. We find that absorbing aerosols aloft in winter 2012 and 2013 heat the middle‐ and lower troposphere by ∼0.5–1 K, reducing cloud liquid water, snowfall, and snow cover. The subsequent decline in surface albedo appears to counteract the ∼15–20 W m−2decrease in shortwave radiation reaching the surface due to attenuation by aerosols overhead. The net result of this novel cloud‐snowfall‐albedo feedback in winters 2012–2013 is a slight increase in surface temperature of ∼0.5–1 K in some regions and little change elsewhere. The aerosol heating aloft, however, stabilizes the atmosphere and decreases the seasonal mean planetary boundary layer (PBL) height by ∼50 m. In winter 2016 and 2017, the ∼20% decrease in mean PM2.5weakens the cloud‐snowfall‐albedo feedback, though it is still evident in western China, where the feedback again warms the surface by ∼0.5–1 K. Regardless of emissions, we find that aerosol‐radiation interactions enhance mean surface PM2.5pollution by 10%–20% across much of China during all four winters examined, mainly though suppression of PBL heights.