Aerosol optical properties along the northeast coast of North America during the New England Air Quality Study-Intercontinental Transport and Chemical Transformation 2004 campaign and the influence of aerosol composition

2007 ◽  
Vol 112 (D10) ◽  
Author(s):  
Wei Wang ◽  
Mark J. Rood ◽  
Christian M. Carrico ◽  
David S. Covert ◽  
Patricia K. Quinn ◽  
...  
2021 ◽  
Author(s):  
Meloë S. F. Kacenelenbogen ◽  
Qian Tan ◽  
Sharon P. Burton ◽  
Otto P. Hasekamp ◽  
Karl D. Froyd ◽  
...  

Abstract. Improvements in air quality and Earth’s climate predictions require improvements of the aerosol speciation in chemical transport models, using observational constraints. Aerosol speciation (e.g., organic aerosols, black carbon, sulfate, nitrate, ammonium, dust or sea salt) is typically determined using in situ instrumentation. Continuous, routine surface network aerosol composition measurements are not uniformly widespread over the globe. Satellites, on the other hand, can provide a maximum coverage of the horizontal and vertical atmosphere but observe aerosol optical properties (and not aerosol speciation) based on remote sensing instrumentation. Combinations of satellite-derived aerosol optical properties can inform on air mass aerosol types (AMTs e.g., clean marine, dust, polluted continental). However, these AMTs are subjectively defined, might often be misclassified and are hard to relate to the critical parameters that need to be refined in models. In this paper, we derive AMTs that are more directly related to sources and hence to speciation. They are defined, characterized, and derived using simultaneous in situ gas-phase, chemical and optical instruments on the same aircraft during the Study of Emissions and Atmospheric Composition, Clouds, and Climate Coupling by Regional Surveys (SEAC4RS, US, summer of 2013). First, we prescribe well-informed AMTs that display distinct aerosol chemical and optical signatures to act as a training AMT dataset. These in situ observations reduce the errors and ambiguities in the selection of the AMT training dataset. We also investigate the relative skill of various combinations of aerosol optical properties to define AMTs and how much these optical properties can capture dominant aerosol speciation. We find distinct optical signatures for biomass burning (from agricultural or wildfires), biogenic and dust-influence AMTs. Useful aerosol optical properties to characterize these signatures are the extinction angstrom exponent (EAE), the single scattering albedo, the difference of single scattering albedo in two wavelengths, the absorption coefficient, the absorption angstrom exponent (AAE), and the real part of the refractive index (RRI). We find that all four AMTs studied when prescribed using mostly airborne in situ gas measurements, can be successfully extracted from at least three combinations of airborne in situ aerosol optical properties (e.g., EAE, AAE and RRI) over the US during SEAC4RS. However, we find that the optically based classifications for BB from agricultural fires and polluted dust include a large percentage of misclassifications that limit the usefulness of results relating to those classes. The technique and results presented in this study are suitable to develop a representative, robust and diverse source-based AMT database. This database could then be used for widespread retrievals of AMTs using existing and future remote sensing suborbital instruments/networks. Ultimately, it has the potential to provide a much broader observational aerosol data set to evaluate chemical transport and air quality models than is currently available by direct in situ measurements. This study illustrates how essential it is to explore existing airborne datasets to bridge chemical and optical signatures of different AMTs, before the implementation of future spaceborne missions (e.g., the next generation of Earth Observing System (EOS) satellites addressing Aerosol, Cloud, Convection and Precipitation (ACCP) designated observables).


Author(s):  
Lawrence I. Kleinman ◽  
Peter H. Daum ◽  
Yin-Nan Lee ◽  
Gunnar I. Senum ◽  
Stephen R. Springston ◽  
...  

2007 ◽  
Vol 112 (D10) ◽  
Author(s):  
D. E. Wolfe ◽  
W. A. Brewer ◽  
S. C. Tucker ◽  
A. B. White ◽  
D. E. White ◽  
...  

2020 ◽  
Author(s):  
Mahtab Majdzadeh ◽  
Craig Stroud ◽  
Ayodeji Akingunola ◽  
Paul Makar ◽  
Christopher Sioris ◽  
...  

<p>The radiative transfer module of an on-line chemical transport models requires input data from aerosol extinction efficiency, single scatter albedo and asymmetry factor, in order to predict the radiative state of the atmosphere. These aerosol optical properties (aerosol optical depth, AOD), may be integrated vertically for comparison to satellite observations. These optical effects may also influence the shorter wavelengths associated with atmospheric gas photolysis, influencing atmospheric reactivity. These processes may be harmonized in an on-line reaction transport model, such as Environment and Climate Change Canada’s GEM-MACH (GEM: Global Environmental Multi-scale – MACH: Modelling Air quality and Chemistry). Previous photolysis routine in the radiative transfer module, MESSY-JVAL (Modular Earth Sub-Model System), in GEM-MACH, made use of a climatology of aerosol optical properties, and the previous on-line version made use of a homogeneous mixture Mie code for meteorological radiative transfer calculations.</p><p>We calculated a new lookup table for the extinction efficiency, absorption and scattering cross sections of each aerosol type. The new version of MESSY-JVAL uses GEM-MACH predicted aerosol size distributions, chemical composition and relative humidity in each vertical column at each time step as input, reads aerosol absorption and scattering cross section data from the new lookup table and calculates aerosol optical properties, that are then used to modify both photolysis and meteorological radiative transfer calculations.</p><p>In order to evaluate these modifications to the model, we performed a series of simulations with GEM-MACH with wildfire emissions inputs from the Canadian Forest Fire Emissions Prediction System (CFFEPS) and compared the model AOD output with satellite and AERONET (Aerosol Robotic Network) measurement data. Comparison of the hourly AERONET and monthly-averaged satellite AOD demonstrates major improvements in the revised model AOD predictions. The impact of the updated photolysis rates and meteorological radiative transfer calculations on predictions of oxidant mixing ratios and rates of pollutant oxidation (nitrogen dioxide conversion to nitric acid) will be assessed both within and below the forest fire plume.</p>


2020 ◽  
Author(s):  
Sudeep Das ◽  
Govindan Pandithurai

<p>Long term trends of various aerosol optical properties are observed over the city of Pune, the ninth most populated city in India using ground and satellite based instruments such as AERONET, MODIS (Aqua and Terra), MISR, CALIOP and reanalysis tool MERRA. Annually, the Aerosol Optical Depth is observed to be increasing over all the types of instruments (2004-17) with values of 0.01 to 0.006 yr<sup>-1</sup>, whereas the Angstrom exponent has a negative slope (AERONET) which suggests that the fine aerosols are decreasing. Single scattering albedo (SSA) is also increasing (0.00657 yr<sup>-1</sup>), which means the emission of smaller darker particles like soot has decreased over the years. MISR shows that the Absorbing AOD trend is decreasing in the overall study period (-0.0001237 yr<sup>-1</sup>). All these annual trends are related to anthropogenic activities and show differing trends before and after 2008, the year when various pollution counter measures were introduced mainly in Pune and also in various nearby areas. After 2008, the AOD increasing slope reduces, and the AAOD reverses the trend from positive to a negative slope. The average height till various kinds of aerosols reach and their vertical profile is studied using CALIOP data. Monthly variations of AOD and their vertical distribution also observed and discussed. Aerosol characterization is done using the MERRA tool into dust, sea salt, sulfates, elementary carbon, and organic carbon. Their monthly variations are explained by source characterizations using the HySplit model. In summer, air from the Arabian sea brings in dust and sea salt into the city and in winter, aerosols come from central India dominantly as carbon and sulfates changing the air quality over there. This study lays its stress on the fact that even though aerosols cover over a city is mostly non-local, anthropogenic activities of that area do play a significant role and here the city of Pune is a role model to show how measures can be taken to improve air quality over any urban area.</p>


2016 ◽  
Vol 16 (7) ◽  
pp. 4693-4706 ◽  
Author(s):  
Megan D. Willis ◽  
Robert M. Healy ◽  
Nicole Riemer ◽  
Matthew West ◽  
Jon M. Wang ◽  
...  

Abstract. The climatic impacts of black carbon (BC) aerosol, an important absorber of solar radiation in the atmosphere, remain poorly constrained and are intimately related to its particle-scale physical and chemical properties. Using particle-resolved modelling informed by quantitative measurements from a soot-particle aerosol mass spectrometer, we confirm that the mixing state (the distribution of co-emitted aerosol amongst fresh BC-containing particles) at the time of emission significantly affects BC-aerosol optical properties even after a day of atmospheric processing. Both single particle and ensemble aerosol mass spectrometry observations indicate that BC near the point of emission co-exists with hydrocarbon-like organic aerosol (HOA) in two distinct particle types: HOA-rich and BC-rich particles. The average mass fraction of black carbon in HOA-rich and BC-rich particle classes was  < 0.1 and 0.8, respectively. Notably, approximately 90 % of BC mass resides in BC-rich particles. This new measurement capability provides quantitative insight into the physical and chemical nature of BC-containing particles and is used to drive a particle-resolved aerosol box model. Significant differences in calculated single scattering albedo (an increase of 0.1) arise from accurate treatment of initial particle mixing state as compared to the assumption of uniform aerosol composition at the point of BC injection into the atmosphere.


2006 ◽  
Vol 111 (D23) ◽  
Author(s):  
James M. Roberts ◽  
Mathew Marchewka ◽  
Steven B. Bertman ◽  
Paul Goldan ◽  
William Kuster ◽  
...  

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