Impact of emissions from a single urban source on air quality estimated from mobile observation and WRF-STILT model simulations

Author(s):  
Hao Fan ◽  
Chuanfeng Zhao ◽  
Yikun Yang ◽  
Xingchuan Yang ◽  
Chunying Wang
2008 ◽  
Vol 47 (7) ◽  
pp. 1853-1867 ◽  
Author(s):  
Tanya L. Otte

Abstract It is common practice to use Newtonian relaxation, or nudging, throughout meteorological model simulations to create “dynamic analyses” that provide the characterization of the meteorological conditions for retrospective air quality model simulations. Given the impact that meteorological conditions have on air quality simulations, it has been assumed that the resultant air quality simulations would be more skillful by using dynamic analyses rather than meteorological forecasts to characterize the meteorological conditions, and that the statistical trends in the meteorological model fields are also reflected in the air quality model. This article, which is the first of two parts, demonstrates the impact of nudging in the meteorological model on retrospective air quality model simulations. Here, meteorological simulations are generated by the fifth-generation Pennsylvania State University–National Center for Atmospheric Research Mesoscale Model (MM5) using both the traditional dynamic analysis approach and using forecasts for a summertime period. The resultant fields are then used to characterize the meteorological conditions for emissions processing and air quality simulations using the Community Multiscale Air Quality (CMAQ) Modeling System. As expected, on average, the near-surface meteorological fields show a significant degradation over time in the forecasts (when nudging is not used), while the dynamic analyses maintain nearly constant statistical scores in time. The use of nudged MM5 fields in CMAQ generally results in better skill scores for daily maximum 1-h ozone mixing ratio simulations. On average, the skill of the daily maximum 1-h ozone simulation deteriorates significantly over time when nonnudged MM5 fields are used in CMAQ. The daily maximum 1-h ozone mixing ratio also degrades over time in the CMAQ simulation that uses MM5 dynamic analyses, although to a much lesser degree, despite no aggregate loss of skill over time in the dynamic analyses themselves. These results affirm the advantage of using nudging in MM5 to create the meteorological characterization for CMAQ for retrospective simulations, and it is shown that MM5-based dynamic analyses are robust at the surface throughout 5.5-day simulations.


Author(s):  
K. L. Chan ◽  
K. Qin

In this study, we present a quantitative estimation of the impacts of biomass burning emissions from different source regions to the local air quality in Hong Kong in 2014 using global chemistry transport model simulations, sun photometer measurements, satellite observations and local monitoring network data. This study focuses on two major biomass burning pollutants, black carbon aerosols and carbon monoxide (CO). The model simulations of atmospheric black carbon and CO show excellent agreement with sun photometer aerosol optical depth (AOD) measurements, satellite CO columns observations and local monitoring stations data. From the model simulation results, we estimated that biomass burning contributes 12 % of total black carbon and 16 % of atmospheric CO in Hong Kong on annual average. South East Asia shows the largest influence to the black carbon and CO levels in Hong Kong, accounts for 11 % of the total atmospheric black carbon and 8 % of CO. Biomass burning in North East Asia and Africa also show significant impacts to Hong Kong. Elevated levels of atmospheric black carbon aerosols and CO were observed during springtime (March and April) which is mainly due to the enhancement of biomass burning contributions. Black carbon and CO originating from biomass burning sources are estimated to contribute 40 % of atmospheric black carbon and 28 % of CO in Hong Kong during March 2014. An investigation focusing on the biomass burning pollution episode during springtime suggests the intensified biomass burning activities in the Indochinese Peninsula are the major sources of black carbon and CO in Hong Kong during the time.


2010 ◽  
Vol 3 (1) ◽  
pp. 169-188 ◽  
Author(s):  
K. W. Appel ◽  
S. J. Roselle ◽  
R. C. Gilliam ◽  
J. E. Pleim

Abstract. This paper presents a comparison of the operational performances of two Community Multiscale Air Quality (CMAQ) model v4.7 simulations that utilize input data from the 5th-generation Mesoscale Model (MM5) and the Weather Research and Forecasting (WRF) meteorological models. Two sets of CMAQ model simulations were performed for January and August 2006. One set utilized MM5 meteorology (MM5-CMAQ) and the other utilized WRF meteorology (WRF-CMAQ), while all other model inputs and options were kept the same. For January, predicted ozone (O3) mixing ratios were higher in the Southeast and lower Mid-west regions in the WRF-CMAQ simulation, resulting in slightly higher bias and error as compared to the MM5-CMAQ simulations. The higher predicted O3 mixing ratios are attributed to less dry deposition of O3 in the WRF-CMAQ simulation due to differences in the calculation of the vegetation fraction between the MM5 and WRF models. The WRF-CMAQ results showed better performance for particulate sulfate (SO42−), similar performance for nitrate (NO3−), and slightly worse performance for nitric acid (HNO3), total carbon (TC) and total fine particulate (PM2.5) mass than the corresponding MM5-CMAQ results. For August, predictions of O3 were notably higher in the WRF-CMAQ simulation, particularly in the southern United States, resulting in increased model bias. Concentrations of predicted particulate SO42− were lower in the region surrounding the Ohio Valley and higher along the Gulf of Mexico in the WRF-CMAQ simulation, contributing to poorer model performance. The primary causes of the differences in the MM5-CMAQ and WRF-CMAQ simulations appear to be due to differences in the calculation of wind speed, planetary boundary layer height, cloud cover and the friction velocity (u∗) in the MM5 and WRF model simulations, while differences in the calculation of vegetation fraction and several other parameters result in smaller differences in the predicted CMAQ model concentrations. The performance for SO42−, NO3− and NH4+ wet deposition was similar for both simulations for January and August.


2011 ◽  
Vol 4 (2) ◽  
pp. 357-371 ◽  
Author(s):  
K. W. Appel ◽  
K. M. Foley ◽  
J. O. Bash ◽  
R. W. Pinder ◽  
R. L. Dennis ◽  
...  

Abstract. This paper examines the operational performance of the Community Multiscale Air Quality (CMAQ) model simulations for 2002–2006 using both 36-km and 12-km horizontal grid spacing, with a primary focus on the performance of the CMAQ model in predicting wet deposition of sulfate (SO4=), ammonium (NH4+) and nitrate (NO3−). Performance of the wet deposition estimates from the model is determined by comparing CMAQ predicted concentrations to concentrations measured by the National Acid Deposition Program (NADP), specifically the National Trends Network (NTN). For SO4= wet deposition, the CMAQ model estimates were generally comparable between the 36-km and 12-km simulations for the eastern US, with the 12-km simulation giving slightly higher estimates of SO4= wet deposition than the 36-km simulation on average. The result is a slightly larger normalized mean bias (NMB) for the 12-km simulation; however both simulations had annual biases that were less than ±15 % for each of the five years. The model estimated SO4= wet deposition values improved when they were adjusted to account for biases in the model estimated precipitation. The CMAQ model underestimates NH4+ wet deposition over the eastern US, with a slightly larger underestimation in the 36-km simulation. The largest underestimations occur in the winter and spring periods, while the summer and fall have slightly smaller underestimations of NH4+ wet deposition. The underestimation in NH4+ wet deposition is likely due in part to the poor temporal and spatial representation of ammonia (NH3) emissions, particularly those emissions associated with fertilizer applications and NH3 bi-directional exchange. The model performance for estimates of NO3− wet deposition are mixed throughout the year, with the model largely underestimating NO3− wet deposition in the spring and summer in the eastern US, while the model has a relatively small bias in the fall and winter. Model estimates of NO3− wet deposition tend to be slightly lower for the 36-km simulation as compared to the 12-km simulation, particularly in the spring. The underestimation of NO3− wet deposition in the spring and summer is due in part to a lack of lightning generated NO emissions in the upper troposphere, which can be a large source of NO in the spring and summer when lightning activity is the high. CMAQ model simulations that include production of NO from lightning show a significant improvement in the NO3− wet deposition estimates in the eastern US in the summer. Overall, performance for the 36-km and 12-km CMAQ model simulations is similar for the eastern US, while for the western US the performance of the 36-km simulation is generally not as good as either eastern US simulation, which is not entire unexpected given the complex topography in the western US.


2008 ◽  
Vol 42 (21) ◽  
pp. 5403-5412 ◽  
Author(s):  
John S. Irwin ◽  
Kevin Civerolo ◽  
Christian Hogrefe ◽  
Wyat Appel ◽  
Kristen Foley ◽  
...  

2020 ◽  
Author(s):  
Isaac Kwadjo Afreh ◽  
Bernard Aumont ◽  
Marie Camredon ◽  
Kelley Claire Barsanti

Abstract. Camphene, a dominant monoterpene emitted from both biogenic and pyrogenic sources, has been significantly understudied, particularly in regard to secondary organic aerosol (SOA) formation. When camphene represents a significant fraction of emissions, the lack of model parameterizations for camphene can result in inadequate representation of gas-phase chemistry and underprediction of SOA formation. In this work, the first mechanistic study of SOA formation from camphene was performed using the Generator for Explicit Chemistry and Kinetics of Organics in the Atmosphere (GECKO-A). GECKO-A was used to generate gas-phase chemical mechanisms for camphene and two well-studied monoterpenes, α-pinene and limonene; and to predict SOA mass formation and composition based on gas/particle partitioning theory. The model simulations represented observed trends in published gas-phase reaction pathways and SOA yields well under chamber-relevant photooxidation and dark ozonolysis conditions. For photooxidation conditions, 70 % of the simulated α-pinene oxidation products remained in the gas phase compared to 50 % for limonene; supporting model predictions and observations of limonene having higher SOA yields than α-pinene under equivalent conditions. The top 10 simulated particle-phase products in the α-pinene and limonene simulations represented 37–50 % of the SOA mass formed and 6–27 % of the hydrocarbon mass reacted. To facilitate comparison of camphene with α-pinene and limonene, model simulations were run under idealized atmospheric conditions, wherein the gas-phase oxidant levels were controlled. Metrics for comparison included: gas-phase reactivity profiles, time-evolution of SOA mass and yields, and physicochemical property distributions of gas- and particle-phase products. The controlled-reactivity simulations demonstrated that: (1) in the early stages of oxidation, camphene is predicted to form very low volatility products, lower than α-pinene and limonene, which condense at low mass loadings; and (2) the final simulated SOA yield for camphene (46 %) was relatively high, in between α-pinene (25 %) and limonene (74 %). A 50 / 50 (α-pinene / limonene) mixture was then used as a surrogate to represent SOA formation from camphene; while simulated SOA mass and yield were well represented, the volatility distribution of the particle-phase products was not. To demonstrate the potential importance of including a parameterized representation of SOA formation by camphene in air quality models, SOA mass and yield were predicted for three wildland fire fuels based on measured monoterpene distributions, and published SOA parameterizations for α-pinene and limonene. Using the 50 / 50 surrogate mixture to represent camphene increased predicted SOA mass by 43–50 % for black spruce and by 56–108 % for Douglas fir. This first detailed modeling study of the gas-phase oxidation of camphene and subsequent SOA formation provides an opportunity for future measurement-model comparisons and lays the foundation for developing chemical mechanism and SOA parameterizations for camphene that are suitable for air quality modeling.


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