scholarly journals Review of “Properties of biomass burning aerosol mixtures derived at fine temporal and spatial scales from Raman lidar measurements: Part I optical properties” by Janicka and Stachlewska

2019 ◽  
Author(s):  
Anonymous
2019 ◽  
Author(s):  
Lucja Janicka ◽  
Iwona S. Stachlewska

Abstract. The analysis of the aerosol optical properties derived at fine temporal and spatial scales were performed based on measurements obtained during heat wave event in vicinity of a cold weather front in Warsaw on August 9th–11th, 2015. The signals collected by the PollyXT-UW lidar allowed for the calculation of 23 sets of so-called 3β + 2α + 2δ + wv profiles averaged by 30-minutes periods during 2 nights. The total number of 11 different aerosol types and aerosol mixtures were identified with reference to properties within 116 sub-layers in the profiles and were characterized by the mean values. The statistical sample of various optical properties being in agreement for consecutive profiles allowed to assess the spatio-temporal extent of aerosol/mixture types. The mean lidar ratio values of 53–73 sr (355 nm) and 31–45 sr (532 nm) in the layers dominated by the anthropogenic pollution were found. For the layers dominated by the biomass burning aerosol (fresh, moderately fresh, moderately aged) mean lidar ratio was of 69–114 sr (355 nm) and 57–85 sr (532 nm). The colour ratio of lidar ratio (532 / 355) higher than 1, characteristic for aged biomass burning aerosol, was found only in one scattered layer, accompanying with low value of extinction related Ångström exponent of 0.60 ± 0.32 and low particle depolarization ratio. The maximum of the particle depolarization ratio of 4.8–5.0 % at 532 nm were observed in a layer likely contaminated with pollen and in a layer dominated by fresh biomass burning aerosol. This study provides an excellent data set for exploration of separation algorithms, aerosol typing algorithms and microphysical inversion.


2015 ◽  
Vol 15 (10) ◽  
pp. 5429-5442 ◽  
Author(s):  
E. Giannakaki ◽  
A. Pfüller ◽  
K. Korhonen ◽  
T. Mielonen ◽  
L. Laakso ◽  
...  

Abstract. Raman lidar data obtained over a 1 year period has been analysed in relation to aerosol layers in the free troposphere over the Highveld in South Africa. In total, 375 layers were observed above the boundary layer during the period 30 January 2010 to 31 January 2011. The seasonal behaviour of aerosol layer geometrical characteristics, as well as intensive and extensive optical properties were studied. The highest centre heights of free-tropospheric layers were observed during the South African spring (2520 ± 970 m a.g.l., also elsewhere). The geometrical layer depth was found to be maximum during spring, while it did not show any significant difference for the rest of the seasons. The variability of the analysed intensive and extensive optical properties was high during all seasons. Layers were observed at a mean centre height of 2100 ± 1000 m with an average lidar ratio of 67 ± 25 sr (mean value with 1 standard deviation) at 355 nm and a mean extinction-related Ångström exponent of 1.9 ± 0.8 between 355 and 532 nm during the period under study. Except for the intensive biomass burning period from August to October, the lidar ratios and Ångström exponents are within the range of previous observations for urban/industrial aerosols. During Southern Hemispheric spring, the biomass burning activity is clearly reflected in the optical properties of the observed free-tropospheric layers. Specifically, lidar ratios at 355 nm were 89 ± 21, 57 ± 20, 59 ± 22 and 65 ± 23 sr during spring (September–November), summer (December–February), autumn (March–May) and winter (June–August), respectively. The extinction-related Ångström exponents between 355 and 532 nm measured during spring, summer, autumn and winter were 1.8 ± 0.6, 2.4 ± 0.9, 1.8 ± 0.9 and 1.8 ± 0.6, respectively. The mean columnar aerosol optical depth (AOD) obtained from lidar measurements was found to be 0.46 ± 0.35 at 355 nm and 0.25 ± 0.2 at 532 nm. The contribution of free-tropospheric aerosols on the AOD had a wide range of values with a mean contribution of 46%.


2007 ◽  
Vol 7 (4) ◽  
pp. 12657-12686 ◽  
Author(s):  
K. Hungershöfer ◽  
K. Zeromskiene ◽  
Y. Iinuma ◽  
G. Helas ◽  
J. Trentmann ◽  
...  

Abstract. A better characterisation of the optical properties of biomass burning aerosol as a function of the burning conditions is required in order to quantify their effects on climate and atmospheric chemistry. Controlled laboratory combustion experiments with different fuel types were carried out at the combustion facility of the Max Planck Institute for Chemistry (Mainz, Germany) as part of the 'Impact of Vegetation Fires on the Composition and Circulation of the Atmosphere' (EFEU) project. Using the measured size distributions as well as mass scattering and absorption efficiencies, Mie calculations provided mean effective refractive indices of 1.60−0.010i and 1.56−0.010i (λ=0.55 μm) for smoke particles emitted from the combustion of savanna grass and an African hardwood (musasa), respectively. The relatively low imaginary parts suggest that the light-absorbing carbon of the investigated fresh biomass burning aerosol is only partly graphitized, resulting in strongly scattering and less absorbing particles. While the observed variability in mass scattering efficiencies was consistent with changes in particle size, the changes in the mass absorption efficiency can only be explained, if the chemical composition of the particles varies with combustion conditions.


2015 ◽  
Vol 8 (9) ◽  
pp. 3789-3809 ◽  
Author(s):  
K. Baibakov ◽  
N. T. O'Neill ◽  
L. Ivanescu ◽  
T. J. Duck ◽  
C. Perro ◽  
...  

Abstract. We present recent progress on nighttime retrievals of aerosol and cloud optical properties over the PEARL (Polar Environmental Atmospheric Research Laboratory) station at Eureka (Nunavut, Canada) in the High Arctic (80° N, 86° W). In the spring of 2011 and 2012, a star photometer was employed to acquire aerosol optical depth (AOD) data, while vertical aerosol and cloud backscatter profiles were measured using the CANDAC Raman Lidar (CRL). We used a simple backscatter coefficient threshold (βthr) to distinguish aerosols from clouds and, assuming that aerosols were largely fine mode (FM)/sub-micron, to distinguish FM aerosols from coarse mode (CM)/super-micron cloud or crystal particles. Using prescribed lidar ratios, we computed FM and CM AODs that were compared with analogous AODs estimated from spectral star photometry. We found (βthr dependent) coherences between the lidar and star photometer for both FM events and CM cloud and crystal events with averaged, FM absolute differences being


2019 ◽  
Vol 19 (14) ◽  
pp. 9181-9208 ◽  
Author(s):  
Kristina Pistone ◽  
Jens Redemann ◽  
Sarah Doherty ◽  
Paquita Zuidema ◽  
Sharon Burton ◽  
...  

Abstract. The total effect of aerosols, both directly and on cloud properties, remains the biggest source of uncertainty in anthropogenic radiative forcing on the climate. Correct characterization of intensive aerosol optical properties, particularly in conditions where absorbing aerosol is present, is a crucial factor in quantifying these effects. The southeast Atlantic Ocean (SEA), with seasonal biomass burning smoke plumes overlying and mixing with a persistent stratocumulus cloud deck, offers an excellent natural laboratory to make the observations necessary to understand the complexities of aerosol–cloud–radiation interactions. The first field deployment of the NASA ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS) campaign was conducted in September of 2016 out of Walvis Bay, Namibia. Data collected during ORACLES-2016 are used to derive aerosol properties from an unprecedented number of simultaneous measurement techniques over this region. Here, we present results from six of the eight independent instruments or instrument combinations, all applied to measure or retrieve aerosol absorption and single-scattering albedo. Most but not all of the biomass burning aerosol was located in the free troposphere, in relative humidities typically ranging up to 60 %. We present the single-scattering albedo (SSA), absorbing and total aerosol optical depth (AAOD and AOD), and absorption, scattering, and extinction Ångström exponents (AAE, SAE, and EAE, respectively) for specific case studies looking at near-coincident and near-colocated measurements from multiple instruments, and SSAs for the broader campaign average over the month-long deployment. For the case studies, we find that SSA agrees within the measurement uncertainties between multiple instruments, though, over all cases, there is no strong correlation between values reported by one instrument and another. We also find that agreement between the instruments is more robust at higher aerosol loading (AOD400>0.4). The campaign-wide average and range shows differences in the values measured by each instrument. We find the ORACLES-2016 campaign-average SSA at 500 nm (SSA500) to be between 0.85 and 0.88, depending on the instrument considered (4STAR, AirMSPI, or in situ measurements), with the interquartile ranges for all instruments between 0.83 and 0.89. This is consistent with previous September values reported over the region (between 0.84 and 0.90 for SSA at 550nm). The results suggest that the differences observed in the campaign-average values may be dominated by instrument-specific spatial sampling differences and the natural physical variability in aerosol conditions over the SEA, rather than fundamental methodological differences.


2017 ◽  
Vol 12 (03) ◽  
pp. P03008-P03008 ◽  
Author(s):  
L. Wiencke ◽  
V. Rizi ◽  
M. Will ◽  
C. Allen ◽  
A. Botts ◽  
...  

2011 ◽  
Vol 38 (1) ◽  
pp. n/a-n/a ◽  
Author(s):  
L. Alados-Arboledas ◽  
D. Müller ◽  
J. L. Guerrero-Rascado ◽  
F. Navas-Guzmán ◽  
D. Pérez-Ramírez ◽  
...  

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