An analysis of AERONET aerosol absorption properties and classifications representative of aerosol source regions

Date

2012-09-06

Department

Program

Citation of Original Publication

Giles, D. M., B. N. Holben, T. F. Eck, A. Sinyuk, A. Smirnov, I. Slutsker, R. R. Dickerson, A. M. Thompson, and J. S. Schafer. “An Analysis of AERONET Aerosol Absorption Properties and Classifications Representative of Aerosol Source Regions.” Journal of Geophysical Research: Atmospheres 117, no. D17 (2012). https://doi.org/10.1029/2012JD018127.

Rights

This work was written as part of one of the author's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law.
Public Domain

Abstract

Partitioning of mineral dust, pollution, smoke, and mixtures using remote sensing techniques can help improve accuracy of satellite retrievals and assessments of the aerosol radiative impact on climate. Spectral aerosol optical depth (τ) and single scattering albedo (ω₀) from Aerosol Robotic Network (AERONET) measurements are used to form absorption (i.e., ω₀ and absorption Ångström exponent (αabs)) and size (i.e., extinction Ångström exponent (αext) and fine mode fraction of τ) relationships to infer dominant aerosol types. Using the long-term AERONET data set (1999–2010), 19 sites are grouped by aerosol type based on known source regions to (1) determine the average ω₀ and αabs at each site (expanding upon previous work), (2) perform a sensitivity study on αabs by varying the spectral ω₀, and (3) test the ability of each absorption and size relationship to distinguish aerosol types. The spectral ω₀ averages indicate slightly more aerosol absorption (i.e., a 0.0 < δω₀ ≤ 0.02 decrease) than in previous work, and optical mixtures of pollution and smoke with dust show stronger absorption than dust alone. Frequency distributions of αabs show significant overlap among aerosol type categories, and at least 10% of the αabs retrievals in each category are below 1.0. Perturbing the spectral ω₀ by ±0.03 induces significant αabs changes from the unperturbed value by at least ∼±0.6 for Dust, ∼±0.2 for Mixed, and ∼±0.1 for Urban/Industrial and Biomass Burning. The ω₀440nm and αext440–870nmrelationship shows the best separation among aerosol type clusters, providing a simple technique for determining aerosol type from surface- and future space-based instrumentation.