The behaviour of the atmospheric aerosol scattering coefficient under varying meteorological conditions

1986 ◽  
Vol 37 (4) ◽  
pp. 175-183 ◽  
Author(s):  
R. Hitzenberger
1980 ◽  
Vol 58 (4) ◽  
pp. 549-553
Author(s):  
A. W. Harrison ◽  
Rosaline Pi

The combined operation of a spectronephelometer and a cascade impactor has been used to study the ratio of differential scattering coefficient (at 550 nm) and mass concentration at mass concentrations of less than 40 µg m−3. Detailed analysis of the mass size distribution impactor data assumed to be near lognormal yielded values of the bulk density in the range 1 to 4 g cm−3. Measurements made in May–June 1978 and in November–December 1978 gave substantially the same results indicating no seasonal variation in either aerosol density or scattering coefficient to mass concentration ratio for mountain and continental background clean air.


2013 ◽  
Vol 13 (10) ◽  
pp. 27811-27854 ◽  
Author(s):  
N. Ma ◽  
W. Birmili ◽  
T. Müller ◽  
T. Tuch ◽  
Y. F. Cheng ◽  
...  

Abstract. This work analyses optical properties of the dry tropospheric aerosol measured at the regional GAW observation site Melpitz in East Germany. For a continuous observation period between 2007 and 2010, we provide representative values of the dry-state scattering coefficient, the hemispheric backscattering coefficient, the absorption coefficient, single scattering albedo, and the Ångström exponent. Besides the direct measurement, the aerosol scattering coefficient was alternatively computed from experimental particle number size distributions using a Mie code. Within pre-defined limits, a closure could be achieved with the direct measurement. The achievement of closure implies that such calculations can be used as a high-level quality control measure for data sets involving multiple instrumentation. All dry optical properties showed significant annual variations, which were attributed to corresponding variations in the regional emission fluxes, the intensity of secondary particle formation, and the mixed layer height. Air mass classification showed that atmospheric stability is a major factor influencing the dry aerosol properties at the GAW station. In the cold season, temperature inversions limit the volume available for atmospheric mixing, so that the aerosol optical properties near the ground proved quite sensitive to the geographical origin of the air mass. In the warm season, when the atmosphere is usually well-mixed during day-time, considerably less variability was observed for the optical properties between different air masses. This work provides, on the basis of quality-checked in-situ measurements, a first step towards a climatological assessment of direct aerosol radiative forcing in the region under study.


2021 ◽  
Vol 14 (7) ◽  
pp. 4879-4891
Author(s):  
Jie Qiu ◽  
Wangshu Tan ◽  
Gang Zhao ◽  
Yingli Yu ◽  
Chunsheng Zhao

Abstract. The aerosol scattering coefficient is an essential parameter for estimating aerosol direct radiative forcing and can be measured by nephelometers. Nephelometers are problematic due to small errors of nonideal Lambetian light source and angle truncation. Hence, the observed raw scattering coefficient data need to be corrected. In this study, based on the random forest machine learning model and taking Aurora 3000 as an example, we have proposed a new method to correct the scattering coefficient measurements of a three-wavelength nephelometer under different relative humidity conditions. The result shows that the empirical corrected values match Mie-calculation values very well at all three wavelengths and under all of the measured relative humidity conditions, with more than 85 % of the corrected values having less than 2 % error. The correction method obtains a scattering coefficient with high accuracy and there is no need for additional observation data.


2019 ◽  
Author(s):  
Carmen Dameto de España ◽  
Gerhard Steiner ◽  
Harald Schuh ◽  
Constantinos Sioutas ◽  
Regina Hitzenberger

Abstract. The ability of atmospheric aerosol particles to act as cloud condensation nuclei (CCN) depends on many factors, including particle size, chemical composition, and meteorological conditions. To expand our knowledge on CCN, it is essential to understand the factors leading to CCN activation. For this purpose a versatile aerosol concentrator enrichment system (VACES) has been modified to select CCN at different supersaturations. The VACES enables to sample CCN particles without altering their chemical and physical properties. The redesigned VACES enriches CCN particles by first passing the aerosol flow to a new saturator and then to a condenser. The activated particles are concentrated by an inertial virtual impactor, and then can be returned to their original size by diffusion-drying. For the calibration, the saturator temperature was fixed at 52 °C and the condenser temperature range was altered from 5 °C to 25 °C to obtain activation curves for NaCl particles of different sizes. Critical water vapour supersaturations can be calculated using the 50 % cutpoint of these curves. Calibration results have also shown that CCN concentrations can be enriched by a factor of approx. 17, which is in agreement with the experimentally determined enrichment factor of the original VACES. The advantage of the re-designed VACES over conventional CCN counters (both static and continuous flow instruments) lies in the substantial enrichment of activated CCN which facilitates further chemical analysis.


2010 ◽  
Vol 10 (2) ◽  
pp. 2889-2914 ◽  
Author(s):  
L. Zhang ◽  
X. Cao ◽  
J. Bao ◽  
B. Zhou ◽  
J. Huang ◽  
...  

Abstract. The vertical distribution of dust aerosol and its radiative properties are analysed using the data measured by the micropulse lidar, profiling microwave radiometer, sunphotometer, particulate monitor, and nephelometer at the Semi-Arid Climate and Environment Observatory of Lanzhou University (SACOL) during a dust storm from 27 March to 29 March 2007. The analysis shows that the dust aerosol mainly exists below 2 km in height, and the dust aerosol extinction coefficient decreases with height. The temporal evolution of aerosol optical depth (AOD) during the dust storm is characterized by a sub-maximum at 22:00 (Beijing Time) on 27 March and a maximum at 12:00 on 28 March. The AOD derived by lidar is compared with that obtained by sunphotometer, and shows a good consistency. The PM10 concentration and aerosol scattering coefficient share identical variation trends, and their maximums both appear at 22:00 on 27 March. The aerosol extinction coefficient and relative humidity have the same trends and their maximums appear at identical heights, showing a correlation between extinction coefficient and relative humidity known as aerosol hygroscopicity. Nevertheless, the correlation between aerosol extinction coefficient and temperature cannot be obviously seen. The aerosol extinction coefficient, scattering coefficient, and PM10 concentration present good linear correlations. The correlation coefficients of the aerosol scattering coefficient and PM10 concentration, of aerosol extinction coefficient and PM10 concentration, and of aerosol extinction and scattering coefficient are respectively 0.98, 0.94, and 0.96.


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