scholarly journals Estimates of ground-level aerosol mass concentrations using a chemical transport model with Moderate Resolution Imaging Spectroradiometer (MODIS) aerosol observations over East Asia

Author(s):  
Yong-Sang Choi ◽  
Rokjin J. Park ◽  
Chang-Hoi Ho
2016 ◽  
Author(s):  
Antigoni Panagiotopoulou ◽  
Panagiotis Charalambidis ◽  
Christos Fountoukis ◽  
Christodoulos Pilinis ◽  
Spyros N. Pandis

Abstract. The ability of the chemical transport model (CTM) PMCAMx to reproduce aerosol optical depth (AOD) measurements by the Aerosol Robotic Network (AERONET) and the Moderate Resolution Imaging Spectroradiometer (MODIS) over Europe during a photochemically active period is evaluated. Periods with high dust levels are excluded so the analysis focuses on the ability of the model to simulate the mostly secondary aerosol and its interactions with water. PMCAMx reproduces the monthly mean MODIS and AERONET AOD values over the Iberian Peninsula, the British Isles, central Europe, and Russia with fractional bias less than 15 % and fractional error less than 30 %. However, the model overestimates the AOD over northern Europe probably due to an overestimation of organic aerosol and sulfates. On the other end, PMCAMx underestimates the monthly mean MODIS AOD over the Balkans, the Mediterranean, and the South Atlantic. These errors are probably due to an underestimation of sulfates. Sensitivity tests indicate that the evaluation results of the monthly mean AODs are quite sensitive to the relative humidity (RH) fields used by PMCAMx, but are not sensitive to the simulated size distribution and the black carbon mixing state.


2017 ◽  
Vol 17 (6) ◽  
pp. 3823-3843 ◽  
Author(s):  
Syuichi Itahashi ◽  
Itsushi Uno ◽  
Kazuo Osada ◽  
Yusuke Kamiguchi ◽  
Shigekazu Yamamoto ◽  
...  

Abstract. High PM2. 5 concentrations of around 100 µg m−3 were observed twice during an intensive observation campaign in January 2015 at Fukuoka (33.52° N, 130.47° E) in western Japan. These events were analyzed comprehensively with a regional chemical transport model and synergetic ground-based observations with state-of-the-art measurement systems, which can capture the behavior of secondary inorganic aerosols (SO42−, NO3−, and NH4+). The first episode of high PM2. 5 concentration was dominated by NO3− (type N) and the second episode by SO42− (type S). The concentration of NH4+ (the counterion for SO42− and NO3−) was high for both types. A sensitivity simulation in the chemical transport model showed that the dominant contribution was from transboundary air pollution for both types. To investigate the differences between these types further, the chemical transport model results were examined, and a backward trajectory analysis was used to provide additional information. During both types of episodes, high concentrations of NO3− were found above China, and an air mass that originated from northeast China reached Fukuoka. The travel time from the coastline of China to Fukuoka differed between types: it was 18 h for type N and 24 h for type S. The conversion ratio of SO2 to SO42− (Fs) was less than 0.1 for type N, but reached 0.3 for type S as the air mass approached Fukuoka. The higher Fs for type S was related to the higher relative humidity and the concentration of HO2, which produces H2O2, the most effective oxidant for the aqueous-phase production of SO42−. Analyzing the gas ratio as an indicator of the sensitivity of NO3− to changes in SO42− and NH4+ showed that the air mass over China was NH3-rich for type N, but almost NH3-neutral for type S. Thus, although the high concentration of NO3− above China gradually decreased during transport from China to Fukuoka, higher NO3− concentrations were maintained during transport owing to the lower SO42− for type N. In contrast, for type S, the production of SO42− led to the decomposition of NH4NO3, and more SO42− was transported. Notably, the type N transport pattern was limited to western Japan, especially the island of Kyushu. Transboundary air pollution dominated by SO42− (type S) has been recognized as a major pattern of pollution over East Asia. However, our study confirms the importance of transboundary air pollution dominated by NO3−, which will help refine our understanding of transboundary heavy PM2. 5 pollution in winter over East Asia.


2016 ◽  
Vol 9 (11) ◽  
pp. 4257-4272
Author(s):  
Antigoni Panagiotopoulou ◽  
Panagiotis Charalampidis ◽  
Christos Fountoukis ◽  
Christodoulos Pilinis ◽  
Spyros N. Pandis

Abstract. The ability of chemical transport model (CTM) PMCAMx to reproduce aerosol optical depth (AOD) measurements by the Aerosol Robotic Network (AERONET) and the Moderate Resolution Imaging Spectroradiometer (MODIS) over Europe during the photochemically active period of May 2008 (EUCAARI campaign) is evaluated. Periods with high dust or sea-salt levels are excluded, so the analysis focuses on the ability of the model to simulate the mostly secondary aerosol and its interactions with water. PMCAMx reproduces the monthly mean MODIS and AERONET AOD values over the Iberian Peninsula, the British Isles, central Europe, and Russia with a fractional bias of less than 15 % and a fractional error of less than 30 %. However, the model overestimates the AOD over northern Europe, most probably due to an overestimation of organic aerosol and sulfates. At the other end, PMCAMx underestimates the monthly mean MODIS AOD over the Balkans, the Mediterranean, and the South Atlantic. These errors appear to be related to an underestimation of sulfates. Sensitivity tests indicate that the evaluation results of the monthly mean AODs are quite sensitive to the relative humidity (RH) fields used by PMCAMx, but are not sensitive to the simulated size distribution and the black carbon mixing state. The screening of the satellite retrievals for periods with high dust (or coarse particles in general) concentrations as well as the combination of the MODIS and AERONET datasets lead to more robust conclusions about the ability of the model to simulate the secondary aerosol components that dominate the AOD during this period.


2019 ◽  
Vol 19 (4) ◽  
pp. 2635-2653 ◽  
Author(s):  
Robyn N. C. Latimer ◽  
Randall V. Martin

Abstract. Aerosol mass scattering efficiency affects climate forcing calculations, atmospheric visibility, and the interpretation of satellite observations of aerosol optical depth. We evaluated the representation of aerosol mass scattering efficiency (αsp) in the GEOS-Chem chemical transport model over North America using collocated measurements of aerosol scatter and mass from IMPROVE network sites between 2000 and 2010. We found a positive bias in mass scattering efficiency given current assumptions of aerosol size distributions and particle hygroscopicity in the model. We found that overestimation of mass scattering efficiency was most significant in dry (RH <35 %) and midrange humidity (35 % < RH <65 %) conditions, with biases of 82 % and 40 %, respectively. To address these biases, we investigated assumptions surrounding the two largest contributors to fine aerosol mass, organic (OA) and secondary inorganic aerosols (SIA). Inhibiting hygroscopic growth of SIA below 35 % RH and decreasing the dry geometric mean radius, from 0.069 µm for SIA and 0.073 µm for OA to 0.058 µm for both aerosol types, significantly decreased the overall bias observed at IMPROVE sites in dry conditions from 82 % to 9 %. Implementation of a widely used alternative representation of hygroscopic growth following κ-Kohler theory for secondary inorganic (hygroscopicity parameter κ=0.61) and organic (κ=0.10) aerosols eliminated the remaining overall bias in αsp. Incorporating these changes in aerosol size and hygroscopicity into the GEOS-Chem model resulted in an increase of 16 % in simulated annual average αsp over North America, with larger increases of 25 % to 45 % in northern regions with high RH and hygroscopic aerosol fractions, and decreases in αsp up to 15 % in the southwestern U.S. where RH is low.


2011 ◽  
Vol 11 (11) ◽  
pp. 5153-5168 ◽  
Author(s):  
A. P. Tsimpidi ◽  
V. A. Karydis ◽  
M. Zavala ◽  
W. Lei ◽  
N. Bei ◽  
...  

Abstract. Urban areas are large sources of organic aerosols and their precursors. Nevertheless, the contributions of primary (POA) and secondary organic aerosol (SOA) to the observed particulate matter levels have been difficult to quantify. In this study the three-dimensional chemical transport model PMCAMx-2008 is used to investigate the temporal and geographic variability of organic aerosol in the Mexico City Metropolitan Area (MCMA) during the MILAGRO campaign that took place in the spring of 2006. The organic module of PMCAMx-2008 includes the recently developed volatility basis-set framework in which both primary and secondary organic components are assumed to be semi-volatile and photochemically reactive and are distributed in logarithmically spaced volatility bins. The MCMA emission inventory is modified and the POA emissions are distributed by volatility based on dilution experiments. The model predictions are compared with observations from four different types of sites, an urban (T0), a suburban (T1), a rural (T2), and an elevated site in Pico de Tres Padres (PTP). The performance of the model in reproducing organic mass concentrations in these sites is encouraging. The average predicted PM1 organic aerosol (OA) concentration in T0, T1, and T2 is 18 μg m−3, 11.7 μg m−3, and 10.5 μg m−3 respectively, while the corresponding measured values are 17.2 μg m−3, 11 μg m−3, and 9 μg m−3. The average predicted locally-emitted primary OA concentrations, 4.4 μg m−3 at T0, 1.2 μg m−3 at T1 and 1.7 μg m−3 at PTP, are in reasonably good agreement with the corresponding PMF analysis estimates based on the Aerosol Mass Spectrometer (AMS) observations of 4.5, 1.3, and 2.9 μg m−3 respectively. The model reproduces reasonably well the average oxygenated OA (OOA) levels in T0 (7.5 μg m−3 predicted versus 7.5 μg m−3 measured), in T1 (6.3 μg m−3 predicted versus 4.6 μg m−3 measured) and in PTP (6.6 μg m−3 predicted versus 5.9 μg m−3 measured). The rest of the OA mass (6.1 μg m−3 and 4.2 μg m−3 in T0 and T1 respectively) is assumed to originate from biomass burning activities and is introduced to the model as part of the boundary conditions. Inside Mexico City (at T0), the locally-produced OA is predicted to be on average 60 % locally-emitted primary (POA), 6 % semi-volatile (S-SOA) and intermediate volatile (I-SOA) organic aerosol, and 34 % traditional SOA from the oxidation of VOCs (V-SOA). The average contributions of the OA components to the locally-produced OA for the entire modelling domain are predicted to be 32 % POA, 10 % S-SOA and I-SOA, and 58 % V-SOA. The long range transport from biomass burning activities and other sources in Mexico is predicted to contribute on average almost as much as the local sources during the MILAGRO period.


2009 ◽  
Vol 9 (20) ◽  
pp. 7901-7911 ◽  
Author(s):  
C.-Y. Lin ◽  
H.-m. Hsu ◽  
Y. H. Lee ◽  
C. H. Kuo ◽  
Y.-F. Sheng ◽  
...  

Abstract. Biomass burning in the Indochina Peninsula (Indochina) is one of the important ozone sources in the low troposphere over East Asia in springtime. Moderate Resolution Imaging Spectroradiometer (MODIS) data show that 20 000 or more active fire detections occurred annually in spring only from 2000 to 2007. In our tracer modeling study, we identify a new mechanism transporting the tracer over Indochina that is significantly different from the vertical transport mechanism over the equatorial areas such as Indonesia and Malaysia. Simulation results demonstrate that the leeside troughs over Indochina play a dominant role in the uplift of the tracer below 3 km, and that the strong westerlies prevailing above 3 km transport the tracer. These fundamental mechanisms have a major impact on the air quality downwind from Indochina over East Asia. The climatological importance of such a leeside trough is also discussed.


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