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The mean physical and optical properties of regional haze dominated by biomass burning aerosol measured from the C‐130 aircraft during SAFARI 2000
328
Citations
51
References
2003
Year
EngineeringAir QualityEarth ScienceOrganic GeochemistryEnvironmental ChemistryGeometric Standard DeviationsAerosol TransportAtmospheric ScienceMicrometeorologyAerosol ConcentrationAerosol SamplingAerosol FormationRadiation MeasurementC‐130 AircraftSafari 2000ClimatologyAtmospheric RadiationRegional HazeAir Pollution
Instrumentation on the Met Office C‐130 aircraft measured aerosol physical and optical properties during the Southern African Regional Science Initiative (SAFARI 2000) in September 2002 while flying from Windhoek, Namibia. Filter measurements of aged regional haze suggest a ratio of apparent elemental carbon (EC a ) to organic carbon (OC) of 0.12 ± 0.02 and mass fractions of 5% EC a , 25% inorganic compounds, and 70% organic matter (OC plus associated elements). The submicron size distribution of aged regional haze may be fitted with three lognormal distributions with geometric mean radii ( r n ) of 0.12 ± 0.01, 0.26 ± 0.01, and 0.80 ± 0.01 μm and geometric standard deviations (σ) of 1.3 ± 0.1, 1.5 ± 0.1, and 1.9 ± 0.4. Measurements over 2500 km from the emission region show similar r n and σ for the smallest two modes, while the third mode is absent presumably as a result of sedimentation. At a wavelength (λ) of 0.55 μm, effective medium approximations suggest a refractive index of 1.54 − 0.018 i for aged regional haze aerosol. The single scattering albedo (ω o λ ) derived using this refractive index and measured size distributions are consistent with those from the nephelometer and Particle Soot Absorption Photometer (PSAP). The optical parameters for aged regional haze a few days old are specific extinction coefficient ( k e λ=0.55 ) of 5.0 ± 0.8 m 2 g −1 , asymmetry factor ( g λ=0.55 ) of 0.59 ± 0.02, and ω o λ=0.55 of 0.91 ± 0.04. Measurements of fresh biomass burning aerosol a few minutes old show smaller more absorbing particles. Vertical profiles of carbon monoxide, aerosol concentration, and aerosol scattering show a good correlation. Over land, aerosols become well mixed in the vertical from the surface to approximately 500 hPa. Over ocean, the aerosols can be separated from underlying stratocumulus cloud by a clear gap and a strong inversion, which may limit the indirect effect.
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