scholarly journals Single-scattering properties of ellipsoidal dust aerosols accounting for realistic shape distributions

2021 ◽  
Author(s):  
Yue Huang ◽  
Jasper Kok ◽  
Olga Munoz Gomez
2019 ◽  
Vol 12 (12) ◽  
pp. 6489-6503
Author(s):  
Hiren Jethva ◽  
Omar Torres

Abstract. The aerosol single-scattering albedo (SSA) retrieved by the near-UV algorithm applied to the Aura Ozone Monitoring Instrument (OMI) measurements (OMAERUV) is compared with an independent inversion product derived from the sky radiometer network SKYNET – a ground-based radiation observation network with sites in Asia and Europe. The present work continues previous efforts to evaluate the consistency between the retrieved SSA from satellite and ground sensors. The automated spectral measurements of direct downwelling solar flux and sky radiances made by the SKYNET Sun-sky radiometer are used as input to an inversion algorithm that derives spectral aerosol optical depth (AOD) and single-scattering albedo (SSA) in the near-UV to near-IR spectral range. The availability of SKYNET SSA measurements in the ultraviolet region of the spectrum allows, for the first time, a direct comparison with OMI SSA retrievals eliminating the need of extrapolating the satellite retrievals to the visible wavelengths as is the case in the evaluation against the Aerosol Robotic Network (AERONET). An analysis of the collocated retrievals from over 25 SKYNET sites reveals that about 61 % (84 %) of OMI–SKYNET matchups agree within the absolute difference of ±0.03 (±0.05) for carbonaceous aerosols, 50 % (72 %) for dust aerosols, and 45 % (75 %) for urban–industrial aerosol types. Regionally, the agreement between the two inversion products is robust over several sites in Japan influenced by carbonaceous and urban–industrial aerosols; at the biomass burning site Phimai in Thailand; and the polluted urban site in New Delhi, India. The collocated dataset yields fewer matchups identified as dust aerosols mostly over the site Dunhuang with more than half of the matchup points confined to within ±0.03 limits. Altogether, the OMI–SKYNET retrievals agree within ±0.03 when SKYNET AOD (388 or 400 nm) is larger than 0.5 and the OMI UV Aerosol Index is larger than 0.2. The remaining uncertainties in both inversion products can be attributed to specific assumptions made in the retrieval algorithms, i.e., the uncertain calibration constant, assumption of spectral surface albedo and particle shape, and subpixel cloud contamination. The assumption of fixed and spectrally neutral surface albedo (0.1) in the SKYNET inversion appears to be unrealistic, leading to underestimated SSA, especially under lower aerosol load conditions. At higher AOD values for carbonaceous and dust aerosols, however, retrieved SSA values by the two independent inversion methods are generally consistent in spite of the differences in retrieval approaches.


2012 ◽  
Vol 117 (D11) ◽  
pp. n/a-n/a ◽  
Author(s):  
Hans Moosmüller ◽  
Johann P. Engelbrecht ◽  
Michał Skiba ◽  
Garrett Frey ◽  
Rajan K. Chakrabarty ◽  
...  

2013 ◽  
Vol 13 (21) ◽  
pp. 10827-10845 ◽  
Author(s):  
M. Yoshida ◽  
J. M. Haywood ◽  
T. Yokohata ◽  
H. Murakami ◽  
T. Nakajima

Abstract. There is great uncertainty regarding the role of mineral dust aerosols in Earth's climate system. One reason for this uncertainty is that the optical properties of mineral dust, such as its single scattering albedo (the ratio of scattering to total extinction), are poorly constrained because ground observations are limited to a few locations and satellite standard products are not available due to the excessively bright surface of the desert in the visible wavelength, which makes robust retrievals difficult. Here, we develop a method to estimate the spatial distributions of the aerosol single scattering albedo (ω0) and optical depth (τa), with daily 1°×1° spatial resolution using data from the Moderate Resolution Imaging Spectroradiometer (MODIS) as well as model simulations of radiative transfer. This approach is based on the "critical surface reflectance" method developed in the literature, which estimates ω0 from the top of the atmospheric radiance. We estimate the uncertainties in ω0 over the Sahara (Asia) to be approximately 0.020 and 0.010 (0.023 and 0.017) for bands 9 and 1, respectively, while the uncertainty in τa is approximately 0.235 and 0.228 (0.464 and 0.370) for bands 9 and 1, respectively. The 5–95% range of the spatial distribution of ω0 over the Sahara (Asia) is approximately 0.90–0.94 and 0.96–0.99 (0.87–0.94 and 0.89–0.97) for bands 9 and 1, respectively, and that of τa over the Sahara (Asia) is approximately 0.8–1.4 and 0.8–1.7 (0.7–2.0 and 0.7–1.9) for bands 9 and 1, respectively. The results for the Sahara indicate a good correlation between ω0 and the surface reflectance, and between ω0 and τa. However, the relationships between ω0, τa, and surface reflectance are less clear in Asia than in the Sahara, and the ω0 values are smaller than those in the Sahara. The regions with small ω0 values are consistent with the regions where coal-burning smoke and carbonaceous aerosols are reported to be transported in previous studies. Because the coal-burning and carbonaceous aerosols are known to be more absorptive and have smaller ω0 values than dust aerosols, our results indicate that the dust aerosols in Asia are contaminated by these anthropogenic aerosols. The spatial distribution of dust optical properties obtained in our work could be useful in understanding the role of dust aerosols in Earth's climate system, most likely through future collaboration with regional and global modelling studies.


2017 ◽  
Author(s):  
Claudia Di Biagio ◽  
Paola Formenti ◽  
Mathieu Cazaunau ◽  
Edouard Pangui ◽  
Nicholas Marchand ◽  
...  

Abstract. In this study we provide a first estimate of the aethalometer multiple scattering correction Cref for mineral dust aerosols. The Cref at 450 and 660 nm was obtained from the direct comparison of aethalometer data (Magee Sci. AE31) with the absorption coefficient calculated as the difference between the extinction and scattering coefficients measured by a CAPS PMex and a nephelometer at 450 nm and the absorption coefficient from a MAAP (Multi-Angle Absorption Photometer) at 660 nm. Measurements were performed on seven dust aerosol samples generated in the laboratory by the mechanical shaking of natural parent soils issued from different source regions worldwide. The single scattering albedo (SSA) at 450 and 660 nm and the size distribution of the aerosols were also measured. Cref for mineral dust varies between 1.81 and 2.56 for a SSA of 0.85–0.96 at 450 nm and between 1.75 and 2.28 for a SSA of 0.98–0.99 at 660 nm. The calculated mean Cref for dust is 2.09 (± 0.22) at 450 nm and 1.92 (± 0.17) at 660 nm. With this new Cref the dust absorption coefficient by aethalometer is about 2 % (450 nm) and 11 % (660 nm) higher than that obtained by using Cref = 2.14, usually assumed in the literature. This difference induces up to 3 % change in the dust SSA. The Cref seems independent of the particle fine and coarse size fractions, and so the obtained Cref can be applied to dust both close to sources and following transport. Additional experiments performed with pure kaolinite mineral and polluted ambient aerosols indicate a Cref of 2.49 (± 0.02) and 2.32 (± 0.01) at 450 and 660 nm (SSA = 0.96–0.97) for kaolinite, and a Cref of 2.32 (± 0.36) at 450 nm and 2.32 (± 0.35) at 660 nm for pollution aerosols (SSA = 0.62–0.87 at 450 nm and 0.42–0.76 at 660 nm).


2012 ◽  
Vol 12 (12) ◽  
pp. 31107-31151
Author(s):  
M. Yoshida ◽  
J. M. Haywood ◽  
B. T. Johnson ◽  
H. Murakami ◽  
T. Nakajima

Abstract. There is a great deal of uncertainty surrounding the role of mineral dust aerosols in the earth's climate system. One reason for this uncertainty is that the optical properties of mineral dust, such as its single scattering albedo (the ratio of scattering to total extinction), are poorly understood because ground observations are limited to several locations and the satellite standard products are not available due to the excessively bright surface of the desert in the visible wavelength. We develop a method in this paper to estimate the spatial distributions of the aerosol single scattering albedo (ω0) and optical depth (τa), with daily 1 degree latitude and 1 degree longitude resolution, using data from Moderate Resolution Imaging Spectroradiometer (MODIS), as well as model simulations of radiative transfer. This approach is based on the "critical surface reflectance" method developed in the literature, which estimates ω0 from the top of the atmospheric radiance. We confirm that the uncertainties in our estimation of ω0 and τa are suitably minor and that the characteristic spatial distributions estimated over the Sahara and Asia are significant. The results for the Sahara indicate good correlation between ω0 and the surface reflectance and between ω0 and τa. Therefore, ω0 is determined mainly by the mineral composition of surface dust and/or the optical depth of airborne dust in the Sahara. On the other hand, the relationships between ω0, τa, and the surface reflectance are less clear in Asia than in the Sahara, and the values of ω0 are smaller than those in the Sahara. The regions with small ω0 values are consistent with the regions where coal-burning smoke and carbonaceous aerosols are thought to be transported, as reported in previous studies. Because the coal-burning and carbonaceous aerosols are known to be more absorptive and have smaller ω0 values than dust aerosols, our results indicate that the dust aerosols in Asia are contaminated by these anthropogenic aerosols. The spatial distribution of dust optical properties obtained in our work could be useful in understanding the roles of dust aerosols in the earth's climate system, most likely through future collaboration with regional and global modelling studies.


2008 ◽  
Vol 8 (4) ◽  
pp. 12461-12528 ◽  
Author(s):  
J.-C. Raut ◽  
P. Chazette

Abstract. This paper presents radiative transfer calculations performed over Niamey in the UV-Visible range over the period 26th January – 1st February during the African Multidisciplinary Monsoon Analysis (AMMA) international program. Climatic effects of aerosols along the vertical column have required an accurate determination of their optical properties, which are presented in for a variety of instrumented platforms: Ultralight aircraft, Facility for Airborne Atmospheric Measurements (FAAM) research aircraft, AERONET station. Measurements highlighted the presence of a multi-layered structure of mineral dust located below and biomass-burning particles in the more elevated layers. Radiative forcing was affected by both the scattering and absorption effects governed by the aerosol complex refractive index (ACRI). The best agreement between our results and AERONET optical thicknesses, ground-based extinction measurements and NO2 photolysis rate coefficient was found using the synergy between all the instrumented platforms. The corresponding averaged ACRI were 1.53 (±0.04)–0.047i (±0.006) and 1.52 (±0.04)–0.008i (±0.001) for biomass-burning and mineral dust aerosols, respectively. Biomass-burning aerosols were characterized by single-scattering albedo ranging from 0.78 to 0.82 and asymmetry parameter ranging from 0.71 to 0.73. For dust aerosols, single-scattering albedo (asymmetry parameter) ranged from 0.9 to 0.92 (0.73 to 0.75). The solar energy depletion at the surface is shown to be ~ −21.2 (±1.7) W/m2 as a daily average. At the TOA, the radiative forcing appeared slightly negative but very close to zero (~ −1.4 W/m2). The corresponding atmospheric radiative forcing was found to be ~19.8 (±2.3) W/m2. Mineral dust located below a more absorbing layer act as an increase in surface reflectivity of ~3–4%. The radiative forcing is also shown to be highly sensitivity the optical features of the different aerosol layers (ACRI, optical thickness and aerosol vertical distribution).


2019 ◽  
Vol 19 (24) ◽  
pp. 15503-15531 ◽  
Author(s):  
Claudia Di Biagio ◽  
Paola Formenti ◽  
Yves Balkanski ◽  
Lorenzo Caponi ◽  
Mathieu Cazaunau ◽  
...  

Abstract. The optical properties of airborne mineral dust depend on its mineralogy, size distribution, and shape, and they might vary between different source regions. To date, large differences in refractive index values found in the literature have not been fully explained. In this paper we present a new dataset of complex refractive indices (m=n-ik) and single-scattering albedos (SSAs) for 19 mineral dust aerosols over the 370–950 nm range in dry conditions. Dust aerosols were generated from natural parent soils from eight source regions (northern Africa, Sahel, Middle East, eastern Asia, North and South America, southern Africa, and Australia). They were selected to represent the global-scale variability of the dust mineralogy. Dust was resuspended into a 4.2 m3 smog chamber where its spectral shortwave scattering (βsca) and absorption (βabs) coefficients, number size distribution, and bulk composition were measured. The complex refractive index was estimated by Mie calculations combining optical and size data, while the spectral SSA was directly retrieved from βsca and βabs measurements. Dust is assumed to be spherical in the whole data treatment, which introduces a potential source of uncertainty. Our results show that the imaginary part of the refractive index (k) and the SSA vary widely from sample to sample, with values for k in the range 0.0011 to 0.0088 at 370 nm, 0.0006 to 0.0048 at 520 nm, and 0.0003 to 0.0021 at 950 nm, as well as values for SSA in the range 0.70 to 0.96 at 370 nm, 0.85 to 0.98 at 520 nm, and 0.95 to 0.99 at 950 nm. In contrast, the real part of the refractive index (n) is mostly source (and wavelength) independent, with an average value between 1.48 and 1.55. The sample-to-sample variability in our dataset of k and SSA is mostly related to differences in the dust iron content. In particular, a wavelength-dependent linear relationship is found between the magnitude of k and SSA and the mass concentrations of both iron oxide and total elemental iron, with iron oxide better correlated than total elemental iron with both k and SSA. The value of k was found to be independent of size. When the iron oxide content exceeds 3 %, the SSA linearly decreases with an increasing fraction of coarse particles at short wavelengths (< 600 nm). Compared to the literature, our values for the real part of the refractive index and SSA are in line with past results, while we found lower values of k compared to most of the literature values currently used in climate models. We recommend that source-dependent values of the SW spectral refractive index and SSA be used in models and remote sensing retrievals instead of generic values. In particular, the close relationships found between k or SSA and the iron content in dust enable the establishment of predictive rules for spectrally resolved SW absorption based on particle composition.


2017 ◽  
Vol 10 (8) ◽  
pp. 2923-2939 ◽  
Author(s):  
Claudia Di Biagio ◽  
Paola Formenti ◽  
Mathieu Cazaunau ◽  
Edouard Pangui ◽  
Nicolas Marchand ◽  
...  

Abstract. In this study we provide a first estimate of the Aethalometer multiple scattering correction Cref for mineral dust aerosols. Cref is an empirical constant used to correct the aerosol absorption coefficient measurements for the multiple scattering artefact of the Aethalometer; i.e. the filter fibres on which aerosols are deposited scatter light and this is miscounted as absorption. The Cref at 450 and 660 nm was obtained from the direct comparison of Aethalometer data (Magee Sci. AE31) with (i) the absorption coefficient calculated as the difference between the extinction and scattering coefficients measured by a Cavity Attenuated Phase Shift Extinction analyser (CAPS PMex) and a nephelometer respectively at 450 nm and (ii) the absorption coefficient from a MAAP (Multi-Angle Absorption Photometer) at 660 nm. Measurements were performed on seven dust aerosol samples generated in the laboratory by the mechanical shaking of natural parent soils issued from different source regions worldwide. The single scattering albedo (SSA) at 450 and 660 nm and the size distribution of the aerosols were also measured. Cref for mineral dust varies between 1.81 and 2.56 for a SSA of 0.85–0.96 at 450 nm and between 1.75 and 2.28 for a SSA of 0.98–0.99 at 660 nm. The calculated mean for dust is 2.09 (±0.22) at 450 nm and 1.92 (±0.17) at 660 nm. With this new Cref the dust absorption coefficient by the Aethalometer is about 2 % (450 nm) and 11 % (660 nm) higher than that obtained by using Cref  =  2.14 at both 450 and 660 nm, as usually assumed in the literature. This difference induces a change of up to 3 % in the dust SSA at 660 nm. The Cref seems to be independent of the fine and coarse particle size fractions, and so the obtained Cref can be applied to dust both close to sources and following transport. Additional experiments performed with pure kaolinite minerals and polluted ambient aerosols indicate Cref of 2.49 (±0.02) and 2.32 (±0.01) at 450 and 660 nm (SSA  =  0.96–0.97) for kaolinite, and Cref of 2.32 (±0.36) at 450 nm and 2.32 (±0.35) at 660 nm for pollution aerosols (SSA  =  0.62–0.87 at 450 nm and 0.42–0.76 at 660 nm).


2008 ◽  
Vol 8 (22) ◽  
pp. 6839-6864 ◽  
Author(s):  
J.-C. Raut ◽  
P. Chazette

Abstract. This paper presents radiative transfer calculations performed over Niamey in the UV-Visible range over the period 26th January–1st February 2006 during the African Multidisciplinary Monsoon Analysis (AMMA) international program. Climatic effects of aerosols along the vertical column have required an accurate determination of their optical properties, which are presented here for a variety of instrumented platforms: Ultralight aircraft, Facility for Airborne Atmospheric Measurements (FAAM) research aircraft, AERONET station. Measurements highlighted the presence of a multi-layered structure of mineral dust located below and biomass-burning particles in the more elevated layers. Radiative forcing was affected by both the scattering and absorption effects governed by the aerosol complex refractive index (ACRI). The best agreement between our results and AERONET optical thicknesses, ground-based extinction measurements and NO2 photolysis rate coefficient was found using the synergy between all the instrumented platforms. The corresponding averaged ACRI at 355 nm were 1.53 (±0.04) −0.047i (±0.006) and 1.52 (±0.04) −0.008i (±0.001) for biomass-burning and mineral dust aerosols, respectively. Biomass-burning aerosols were characterized by single-scattering albedo ranging from 0.78 to 0.82 and asymmetry parameter ranging from 0.71 to 0.73. For dust aerosols, single-scattering albedo (asymmetry parameter) ranged from 0.9 to 0.92 (0.73 to 0.75). The solar energy depletion at the surface is shown to be ~−21.2 (±1.7) W/m2 as a daily average. At the TOA, the radiative forcing appeared slightly negative but very close to zero (~−1.4 W/m2). The corresponding atmospheric radiative forcing was found to be ~19.8 (±2.3) W/m2. Mineral dust located below a more absorbing layer act as an increase in surface reflectivity of ~3–4%. The radiative forcing is also shown to be highly sensitive to the optical features of the different aerosol layers (ACRI, optical thickness and aerosol vertical distribution).


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