Absorption Angstrom Exponent of Dust Aerosols Over the Tarim Basin

Author(s):  
Xiaolin Zhang ◽  
Huan Jiang ◽  
Mao Mao
2013 ◽  
Vol 6 (10) ◽  
pp. 2659-2669 ◽  
Author(s):  
A. Bayat ◽  
H. R. Khalesifard ◽  
A. Masoumi

Abstract. The polarized phase function of atmospheric aerosols has been investigated for the atmosphere of Zanjan, a city in northwest Iran. To do this, aerosol optical depth, Ångström exponent, single-scattering albedo, and polarized phase function have been retrieved from the measurements of a Cimel CE 318-2 polarized sun-photometer from February 2010 to December 2012. The results show that the maximum value of aerosol polarized phase function as well as the polarized phase function retrieved for a specific scattering angle (i.e., 60°) are strongly correlated (R = 0.95 and 0.95, respectively) with the Ångström exponent. The latter has a meaningful variation with respect to the changes in the complex refractive index of the atmospheric aerosols. Furthermore the polarized phase function shows a moderate negative correlation with respect to the atmospheric aerosol optical depth and single-scattering albedo (R = −0.76 and −0.33, respectively). Therefore the polarized phase function can be regarded as a key parameter to characterize the atmospheric particles of the region – a populated city in the semi-arid area and surrounded by some dust sources of the Earth's dust belt.


2006 ◽  
Vol 6 (3) ◽  
pp. 697-713 ◽  
Author(s):  
G. Pace ◽  
A. di Sarra ◽  
D. Meloni ◽  
S. Piacentino ◽  
P. Chamard

Abstract. Aerosol optical depth and Ångström exponent were obtained from multi filter rotating shadowband radiometer (MFRSR) observations carried out at the island of Lampedusa, in the Central Mediterranean, in the period July 2001–September 2003. The average aerosol optical depth at 495.7 nm, τ, is 0.24±0.14; the average Ångström exponent, α, is 0.86±0.63. The observed values of τ range from 0.03 to 1.13, and the values of α vary from −0.32 to 2.05, indicating a large variability in aerosol content and size. In cloud-free conditions, 36% of the airmasses come from Africa, 25% from Central-Eastern Europe, and 19% from Western France, Spain and the North Atlantic. In summer, 42% of the airmasses is of African origin. In almost all cases African aerosols display high values of τ and low values of α, typical of Saharan dust (average values of τ and α are 0.36 and 0.42, respectively). Particles originating from Central-Eastern Europe show relatively large average values of τ and α (0.23 and 1.5, respectively), while particles from Western France, Spain and the North Atlantic show the lowest average values of τ (0.15), and relatively small values of α (0.92). Intermediate values of α are often connected with relatively fast changes of the airmass originating sector, suggesting the contemporary presence of different types of particles in the air column. Clean marine conditions are rare at Lampedusa, and are generally associated with subsidence of the airmasses reaching the island. Average values of τ and α for clean marine conditions are 0.11 and 0.86, respectively. The largest values of α (about 2) were observed in August 2003, when large scale forest fires in Southern Europe produced consistent amounts of fine combustion particles, that were transported to the Central Mediterranean by a persistent high pressure system over Central Europe. Smoke particles in some cases mix with desert dust, producing intermediate values of α. The seasonal distribution of the meteorological patterns over the Mediterranean, the efficiency of the aerosol production mechanisms, and the variability of the particles' residence time produce a distinct seasonal cycle of aerosol optical depths and Ångström exponent values. Particles originating from all sectors show a summer maximum in aerosol optical depth. The summer increase in optical depth for European aerosols is linked with an increment in the values of α, that indicates an enhancement in the number of fine particles. The summer maximum of τ for African particles is associated with a weak reduction in the Ångström exponent, suggesting an increase in the total number of particles and a relatively more intense transport of large particles. The observations were classified according to the aerosol optical properties, and two main classes have been identified: desert dust and biomass burning/urban-industrial aerosols. Values of τ and α averaged over the whole observing period are 0.37 and 0.15 for desert dust, and 0.27 and 1.77 for urban-industrial/biomass burning aerosols.


Atmosphere ◽  
2021 ◽  
Vol 12 (11) ◽  
pp. 1469
Author(s):  
Alba López-Caravaca ◽  
Ramón Castañer ◽  
Alvaro Clemente ◽  
Eduardo Yubero ◽  
Nuria Galindo ◽  
...  

The influence of three Saharan dust events (SDE) on particulate matter (PM) concentrations and aerosol optical properties (AOP) during February 2021 was studied. The physical characteristics of the African aerosol were different for each episode. Therefore, the impacts of the three events on PM and AOP were analyzed separately. The monitoring sites were placed in Elche, in the southeast of the Iberian Peninsula. The sites can be classified as urban background locations. The procedure used to obtain the contribution of SDE to PM10 mass concentrations was the 40th percentile method. Nearly half of the days during the study period were under the influence of Saharan air masses. The average contribution of mineral dust (MD) to the PM10 mean concentration was ~50%, which was the highest contribution during the month of February in the last 14 years. The results show that those events characterized by a high input of fine particles (PM1 and PM2.5) caused larger increases in the absorption (σap) and scattering (σsp) coefficients than SDE in which coarse particles predominated. Nevertheless, as expected, SAE (Scattering Angström Exponent) values were lowest during these episodes. AAE (Absorption Angström Exponent) values during SDE were slightly higher than those observed in the absence of African dust, suggesting some contribution from MD to the absorption process.


2021 ◽  
Vol 14 (10) ◽  
pp. 6419-6441
Author(s):  
Krista Luoma ◽  
Aki Virkkula ◽  
Pasi Aalto ◽  
Katrianne Lehtipalo ◽  
Tuukka Petäjä ◽  
...  

Abstract. We present a comparison between three absorption photometers that measured the absorption coefficient (σabs) of ambient aerosol particles in 2012–2017 at SMEAR II (Station for Measuring Ecosystem–Atmosphere Relations II), a measurement station located in a boreal forest in southern Finland. The comparison included an Aethalometer (AE31), a multi-angle absorption photometer (MAAP), and a particle soot absorption photometer (PSAP). These optical instruments measured particles collected on a filter, which is a source of systematic errors, since in addition to the particles, the filter fibers also interact with light. To overcome this problem, several algorithms have been suggested to correct the AE31 and PSAP measurements. The aim of this study was to research how the different correction algorithms affected the derived optical properties. We applied the different correction algorithms to the AE31 and PSAP data and compared the results against the reference measurements conducted by the MAAP. The comparison between the MAAP and AE31 resulted in a multiple-scattering correction factor (Cref) that is used in AE31 correction algorithms to compensate for the light scattering by filter fibers. Cref varies between different environments, and our results are applicable to a boreal environment. We observed a clear seasonal cycle in Cref, which was probably due to variations in aerosol optical properties, such as the backscatter fraction and single-scattering albedo, and also due to variations in the relative humidity (RH). The results showed that the filter-based absorption photometers seemed to be rather sensitive to the RH even if the RH was kept below the recommended value of 40 %. The instruments correlated well (R≈0.98), but the slopes of the regression lines varied between the instruments and correction algorithms: compared to the MAAP, the AE31 underestimated σabs only slightly (the slopes varied between 0.96–1.00) and the PSAP overestimated σabs only a little (the slopes varied between 1.01–1.04 for a recommended filter transmittance >0.7). The instruments and correction algorithms had a notable influence on the absorption Ångström exponent: the median absorption Ångström exponent varied between 0.93–1.54 for the different algorithms and instruments.


2005 ◽  
Vol 5 (6) ◽  
pp. 11703-11728 ◽  
Author(s):  
V. Aaltonen ◽  
H. Lihavainen ◽  
V.-M. Kerminen ◽  
M. Komppula ◽  
J. Hatakka ◽  
...  

Abstract. Three years of continuous measurements of aerosol optical properties and simultaneous aerosol number size distribution measurements at Pallas GAW station, a remote subarctic site in the northern border of the boreal forest zone, have been analysed. The scattering coefficient at 550 nm varied from 0.2 to 94.4 Mm−1 with an average of 7.1±8.6 Mm−1. Both the scattering and backscattering coefficients had a clear seasonal cycle with an autumn minimum and a 4–5 times higher summer maximum. The scattering was dominated by submicron aerosols and especially so during late summer and autumn. The Ångström exponent had a clear seasonal pattern with maximum values in late summer and minimum values during wintertime. The highest hemispheric backscattering fraction values were observed in autumn, indicating clean air with few scattering particles and a particle size distribution strongly dominated by ultrafine particles. To analyse the influence of air mass origin on the aerosol optical properties a trajectory climatology was applied to the Pallas aerosol data. The most polluted trajectory patterns represented air masses from the Kola Peninsula, Scandinavia and Russia as well as long-range transport from Britain and Eastern Europe. These air masses had the largest average scattering and backscattering coefficients for all seasons. Higher than average values of the Ångström exponent were also observed in connection with transport from these areas.


2019 ◽  
Vol 99 ◽  
pp. 01003
Author(s):  
Athina Avgousta Floutsi ◽  
Marios Bruno Korras Carraca ◽  
Christos Matsoukas ◽  
Nikos Hatzianastassiou ◽  
George Biskos

Central and South Asia are regions of particular interest for studying atmospheric aerosols, being among the largest sources of desert dust aerosols globally. In this study we use the newest collection (C061) of MODIS - Aqua aerosol optical depth (AOD) at 550 nm and Ångström exponent (a) at 412/470 nm over the 15-year period between 2002 and 2017, providing the longest analyzed dataset for this region. According to our results, during spring and summer, high aerosol load (AOD up to 1.2) consisting of coarse desert dust particles, as indicated by a values as low as 0.15, is observed over the Taklamakan, Thar and Registan deserts and the region between the Aral and Caspian seas. The dust load is much lower during winter and autumn (lower AOD and higher a values compared to the other seasons). The interannual variation of AOD and a suggests that the dust load exhibits large decreasing trends (AOD slopes down to -0.22, a slopes up to 0.47 decade-1) over the Thar desert and large increasing trends between the Aral and Caspian seas (AOD and a slopes up to 0.23 decade-1 and down to -0.61 decade-1, respectively.) The AOD data are evaluated against AERONET surface-based measurements. Generally, MODIS and AERONET data are in good agreement with a correlation coefficient (R) equal to 0.835.


Atmosphere ◽  
2020 ◽  
Vol 11 (10) ◽  
pp. 1103
Author(s):  
Jie Luo ◽  
Yongming Zhang ◽  
Qixing Zhang

In this work, the absorption Ångström exponent (AAE), extinction Ångström exponent (EAE), and single-scattering albedo (SSA) of black carbon (BC) with different coating materials are numerically investigated. BC with different coating materials can provide explanations for the small AAE, small EAE, and large AAE observed in the atmosphere, which is difficult to be explained by bare BC aggregate models. The addition of organic carbon (OC) does not necessarily increase AAE due to the transformation of BC morphologies and the existence of non-absorbing OC. The addition of coating materials does also not necessarily decrease EAE. While the addition of coating materials can increase the total size of BC-containing particles, the effective refractive index can be modified by introducing the coating materials, so increases the EAE. We found that it is not possible to differentiate between thinly- and heavily-coated BC based on EAE or AAE alone. On the other hand, SSA is much less sensitive to the size and can provide much more information for distinguishing heavily-coated BC from thinly-coated BC. For BC with different coating materials and mixing states, AAE, EAE, and SSA show rather different sensitivities to particle size and composition ratios, and their spectral-dependences also exhibit distinct differences. Different AAE and EAE trends with BC/OC ratio were also found for BC with different coating materials and mixing states. Furthermore, we also found empirical fittings for AAE, EAE, SSA, and optical cross-sections, which may be useful for retrieving the size information based on the optical measurements.


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