scholarly journals Lidar profiling of aerosol optical properties from Paris to Lake Baikal (Siberia)

2014 ◽  
Vol 14 (20) ◽  
pp. 27881-27944
Author(s):  
E. Dieudonné ◽  
P. Chazette ◽  
F. Marnas ◽  
J. Totems ◽  
X. Shang

Abstract. In June 2013, a ground-based mobile lidar performed the 10 000 km ride from Paris to Ulan-Ude, near Lake Baikal, profiling for the first time aerosol optical properties all the way from Western Europe to central Siberia. The instrument was equipped with N2-Raman and depolarization channels that enabled an optical speciation of aerosols in the low and middle troposphere. The backscatter-to-extinction ratio (BER) and particle depolarization ratio (PDR) at 355 nm have been retrieved. The BER in the lower boundary layer (300–700 m) was found to be 0.017 ± 0.009 sr−1 in average during the campaign, with slightly higher values in background conditions near Lake Baikal (0.021 ± 0.010 sr−1 in average) corresponding to dust-like particles. PDR values observed in Russian cities (>1.7%) are higher than the ones measured in European cities (<1.3%) due to the lifting of terrigenous aerosols by traffic on roads with a bad tarmac. Biomass burning layers from grassland or/and forest fires in southern Russia exhibit BER values ranging from 0.010 to 0.015 sr−1 and from 2 to 3% for the PDR. Desert dust aerosols originating from the Caspian and Aral seas regions were characterized for the first time, with a BER (PDR) of 0.022 sr−1 (21%) for pure dust, and 0.011 sr−1 (15%) for a mix between dust and biomass burning. The lidar observations also showed that this dust event extended over 2300 km and lasted for ~6 days. Measurements from the Moderate Resolution Imaging Spectrometer (MODIS) show that our results are comparable in terms of aerosol optical thickness (between 0.05 and 0.40 at 355 nm) with the mean aerosol load encountered throughout our route.

2015 ◽  
Vol 15 (9) ◽  
pp. 5007-5026 ◽  
Author(s):  
E. Dieudonné ◽  
P. Chazette ◽  
F. Marnas ◽  
J. Totems ◽  
X. Shang

Abstract. In June 2013, a ground-based mobile lidar performed the ~10 000 km ride from Paris to Ulan-Ude, near Lake Baikal, profiling for the first time aerosol optical properties all the way from western Europe to central Siberia. The instrument was equipped with N2-Raman and depolarization channels that enabled an optical speciation of aerosols in the low and middle troposphere. The extinction-to-backscatter ratio (also called lidar ratio or LR) and particle depolarization ratio (PDR) at 355 nm have been retrieved. The LR in the lower boundary layer (300–700 m) was found to be 63 ± 17 sr on average during the campaign with a distribution slightly skewed toward higher values that peaks between 50 and 55 sr. Although the difference is small, PDR values observed in Russian cities (>2%, except after rain) are systematically higher than the ones measured in Europe (<1%), which is probably an effect of the lifting of terrigenous aerosols by traffic on roads. Biomass burning layers from grassland or/and forest fires in southern Russia exhibit LR values ranging from 65 to 107 sr and from 3 to 4% for the PDR. During the route, desert dust aerosols originating from the Caspian and Aral seas regions were characterized for the first time, with a LR (PDR) of 43 ± 14 sr (23 ± 2%) for pure dust. The lidar observations also showed that this dust event extended over 2300 km and lasted for ~6 days. Measurements from the Moderate Resolution Imaging Spectrometer (MODIS) show that our results are comparable in terms of aerosol optical thickness (between 0.05 and 0.40 at 355 nm) with the mean aerosol load encountered throughout our route.


2008 ◽  
Vol 8 (1) ◽  
pp. 3721-3759 ◽  
Author(s):  
J. Vidot ◽  
R. Santer ◽  
O. Aznay

Abstract. The Medium Resolution Imaging Spectrometer (MERIS) launched in February 2002 on-board the ENVISAT spacecraft is making global observations of top-of-atmosphere (TOA) radiances. Aerosol optical properties are retrieved over land using Look-Up Table (LUT) based algorithm and surface reflectances in the blue and the red spectral regions. We compared instantaneous aerosol optical thicknesses retrieved by MERIS in the blue and the red at locations containing sites within the Aerosol Robotic Network (AERONET). Between 2002 and 2005, a set of 500 MERIS images were used in this study. The result shows that, over land, MERIS aerosol optical thicknesses are well retrieved in the blue and poorly retrieved in the red, leading to an underestimation of the Angstrom coefficient. Correlations are improved by applying a simple criterion to avoid scenes probably contaminated by thin clouds. To investigate the weakness of the MERIS algorithm, ground-based radiometer measurements have been used in order to retrieve new aerosol models, based on their Inherent Optical Properties (IOP). These new aerosol models slightly improve the correlation, but the main problem of the MERIS aerosol product over land can be attributed to the surface reflectance model in the red.


2021 ◽  
Vol 21 (1) ◽  
pp. 357-392
Author(s):  
Igor B. Konovalov ◽  
Nikolai A. Golovushkin ◽  
Matthias Beekmann ◽  
Meinrat O. Andreae

Abstract. Long-range transport of biomass burning (BB) aerosol from regions affected by wildfires is known to have a significant impact on the radiative balance and air quality in receptor regions. However, the changes that occur in the optical properties of BB aerosol during long-range transport events are insufficiently understood, limiting the adequacy of representations of the aerosol processes in chemistry transport and climate models. Here we introduce a framework to infer and interpret changes in the optical properties of BB aerosol from satellite observations of multiple BB plumes. Our framework includes (1) a procedure for analysis of available satellite retrievals of the absorption and extinction aerosol optical depths (AAOD and AOD) and single-scattering albedo (SSA) as a function of the BB aerosol photochemical age and (2) a representation of the AAOD and AOD evolution with a chemistry transport model (CTM) involving a simplified volatility basis set (VBS) scheme with a few adjustable parameters. We apply this framework to analyze a large-scale outflow of BB smoke plumes from Siberia toward Europe that occurred in July 2016. We use AAOD and SSA data derived from OMI (Ozone Monitoring Instrument) satellite measurements in the near-UV range along with 550 nm AOD and carbon monoxide (CO) columns retrieved from MODIS (Moderate Resolution Imaging Spectroradiometer) and IASI (Infrared Atmospheric Sounding Interferometer) satellite observations, respectively, to infer changes in the optical properties of Siberian BB aerosol due to its atmospheric aging and to get insights into the processes underlying these changes. Using the satellite data in combination with simulated data from the CHIMERE CTM, we evaluate the enhancement ratios (EnRs) that allow isolating AAOD and AOD changes due to oxidation and gas–particle partitioning processes from those due to other processes, including transport, deposition, and wet scavenging. The behavior of EnRs for AAOD and AOD is then characterized using nonlinear trend analysis. It is found that the EnR for AOD strongly increases (by about a factor of 2) during the first 20–30 h of the analyzed evolution period, whereas the EnR for AAOD does not exhibit a statistically significant increase during this period. The increase in AOD is accompanied by a statistically significant enhancement of SSA. Further BB aerosol aging (up to several days) is associated with a strong decrease in EnRs for both AAOD and AOD. Our VBS simulations constrained by the observations are found to be more consistent with satellite observations of strongly aged BB plumes than “tracer” simulations in which atmospheric transformations of BB organic aerosol were disregarded. The simulation results indicate that the upward trends in EnR for AOD and in SSA are mainly due to atmospheric processing of secondary organic aerosol (SOA), leading to an increase in the mass scattering efficiency of BB aerosol. Evaporation and chemical fragmentation of the SOA species, part of which is assumed to be absorptive (to contain brown carbon), are identified as likely reasons for the subsequent decrease in the EnR for both AAOD and AOD. Hence, our analysis reveals that the long-range transport of smoke plumes from Siberian fires is associated with major changes in BB aerosol optical properties and chemical composition. Overall, this study demonstrates the feasibility of using available satellite observations for evaluating and improving representations in atmospheric models of the BB aerosol aging processes in different regions of the world at much larger temporal scales than those typically addressed in aerosol chamber experiments.


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.


2009 ◽  
Vol 9 (19) ◽  
pp. 7643-7655 ◽  
Author(s):  
B. I. Magi

Abstract. This study characterizes the aerosol over extratropical and tropical southern Africa during the biomass burning season by presenting an aerosol mass apportionment and aerosol optical properties. Carbonaceous aerosol species account for 54% and 83% of the extratropical and tropical aerosol mass, respectively, which is consistent with the fact that the major source of particulate matter in southern Africa is biomass burning. This mass apportionment implies that carbonaceous species in the form of organic carbon (OC) and black carbon (BC) play a critical role in the aerosol optical properties. By combining the in situ measurements of aerosol mass concentrations with concurrent measurements of aerosol optical properties at a wavelength of 550 nm, it is shown that 80–90% of the aerosol scattering is due to carbonaceous aerosol, and the derived mass scattering cross sections (MSC) for OC and BC are 3.9±0.6 m2/g and 1.6±0.2 m2/g, respectively. Derived values of mass absorption cross sections (MAC) for OC and BC are 0.7±0.6 m2/g and 8.2±1.1 m2/g, respectively. The values of MAC imply that ~26% of the aerosol absorption in southern Africa is due to OC, with the remainder due to BC. The results in this study provide important constraints for aerosol properties in a region dominated by biomass burning and should be integrated into climate models to improve aerosol simulations.


2016 ◽  
Author(s):  
M. Ealo ◽  
A. Alastuey ◽  
A. Ripoll ◽  
N. Pérez ◽  
M. C. Minguillón ◽  
...  

Abstract. The study of Saharan dust events (SDE) and biomass burning (BB) emissions are both topic of great scientific interest since they are frequent and important polluting scenarios affecting air quality and climate. The main aim of this work is evaluating the feasibility of using near real-time in situ aerosol optical measurements for the detection of these atmospheric events in the Western Mediterranean Basin (WMB). With this aim, intensive aerosol optical properties (SAE: scattering Ångström exponent, AAE: absorption Ångström exponent, SSAAE: single scattering albedo Ångström exponent, and g: asymmetry parameter) were derived from multi-wavelength aerosol light scattering, hemispheric backscattering and absorption measurements performed at regional (Montseny; MSY, 720 m a.s.l.) and continental (Montsec; MSA, 1570 m a.s.l.) background sites in the WMB. A sensitivity study aiming at calibrating the measured intensive optical properties for SDE and BB detection is presented and discussed. The detection of Saharan dust events (SDE) by means of the SSAAE parameter and Ångström matrix depended on the altitude of the measurement station, and on SDE intensity. At MSA (mountain-top site) SSAAE detected around 85% of SDE compared with 50% at MSY station, where pollution episodes dominated by fine anthropogenic particles frequently masked the effect of mineral dust on optical properties during less intense SDE. Furthermore, an interesting feature of SSAAE was its capability to detect the presence of mineral dust after the end of SDE. Thus, resuspension processes driven by summer regional atmospheric circulations and dry conditions after SDE favored the accumulation of mineral dust at regional level having important consequences for air quality. On average, SAE, AAE and g ranged between -0.7 and 1, 1.3 and 2.5, and 0.5 and 0.75, respectively, during SDE. Based on the Aethalometer model, biomass burning (BB) contribution to equivalent black carbon (BC) accounted for 36% and 40% at MSY and MSA respectively. Linear relationships were found between AAE and %BCbb, with AAE values reaching around 1.5 when %BCbb was higher than 50%. BB contribution to organic matter (OM) at MSY was around 30%. Thus FF combustion sources showed important contributions to both BC and OM in the region under study. Results for OM source apportionment showed good agreement with simultaneous biomass burning organic aerosol (BBOA) and hydrocarbon-like organic aerosol (HOA) calculated from Positive Matrix Factorization (PMF) applied to simultaneous Aerosol Mass Spectrometer (ACSM) measurements. A wildfire episode was identified at MSY, showing AAE values up to 2 when daily BB contributions to BC and OM were 73% and 78% respectively.


2013 ◽  
Author(s):  
Veijo Aaltonen ◽  
Edith Rodriguez ◽  
Larisa Sogacheva ◽  
Pasi Aalto ◽  
Mika Komppula ◽  
...  

2020 ◽  
Author(s):  
Marios Bruno Korras Carraca ◽  
Dimitris Manetas ◽  
David Patoulias ◽  
Spyros Pandis ◽  
Nikolaos Hatzianastassiou ◽  
...  

&lt;p&gt;Natural and anthropogenic aerosol particles are major drivers of the Earth&amp;#8217;s radiation budget, which they affect directly (through scattering and absorption) and indirectly (through modification of cloud scattering and precipitation properties), while they semi-directly influence atmospheric stability and convection, mainly through modification of solar radiation absorption by the atmosphere. Despite the important climatic role of aerosols, large uncertainties in their radiative effects remain due to limited knowledge of the aerosol spatio-temporal distribution and physico-chemical properties. The interaction of aerosols with radiation is strongly dependent on their optical properties, which in turn are controlled by the particles&amp;#8217; size distribution, shape, chemical composition and mixing state. In order to accurately estimate the magnitude of the aerosol direct radiative effect (DRE), detailed knowledge of their optical properties with high spatial and temporal resolution is required.&lt;/p&gt;&lt;p&gt;The European continent is a region of particular interest for studying atmospheric aerosol effects, because of the presence of&amp;#160; numerous and varying sources of particles and their precursors, such as industries, large urban centers and biomass burning, especially when combined with high levels of solar insolation during summer. In this study, the aerosol DRE over Europe is examined using the FORTH deterministic spectral radiative transfer model (RTM) and aerosol data from the chemical transport model PMCAMx. Chemically and size resolved aerosol concentrations predicted by PMCAMx are combined with a Mie model to calculate key aerosol optical properties (i.e. vertically resolved aerosol optical depth, single scattering albedo and asymmetry parameter) that are necessary to compute aerosol DRE using the RTM. The Mie model takes into account concentrations of organics, black carbon, sulfate, nitrate, ammonium, chlorine, sodium, water, and crustal material, and calculates aerosol optical properties assuming that the aerosol particles of the same size are internally mixed. The DRE is estimated at the Earth&amp;#8217;s surface, within the atmospheric column and at the top of the atmosphere (TOA), at high spatial and temporal resolution (36 &amp;#215; 36 km grids, 27 vertical layers, hourly), during June and July 2012.&lt;/p&gt;&lt;p&gt;Initial modelling results reveal that DREs exhibit significant spatio-temporal variability, due to the heterogeneity of source emissions rates, mostly with regard to wildfires, and the varying synoptic conditions. Emphasis is thus given to biomass burning aerosols, which are among the most significant radiative forcing agents in Europe during summer. Their relative forcing is computed by performing model computations with and without biomass burning emissions.&lt;/p&gt;


Author(s):  
D. Rupakheti ◽  
S. Kang ◽  
Z. Cong ◽  
M. Rupakheti ◽  
L. Tripathee ◽  
...  

Atmospheric aerosol possesses impacts on climate system and ecological environments, human health and agricultural productivity. The environment over Himalayas and Tibetan Plateau region are continuously degraded due to the transport of pollution from the foothills of the Himalayas; mostly the Indo-Gangetic Plain (IGP). Thus, analysis of aerosol optical properties over two sites; Lumbini and Kathmandu (the southern slope of central Himalayas) using AERONET’s CIMEL sun photometer were conducted in this study. Aerosol optical depth (AOD at 500&amp;thinsp;nm), angstrom exponent (α or AE), volume size distribution (VSD), single scattering albedo (SSA) and asymmetry parameter (AP) were studied for 2013&amp;ndash;2014 and the average AOD was found to be: 0.64&amp;thinsp;&amp;plusmn;&amp;thinsp;0.41 (Lumbini) and 0.45&amp;thinsp;&amp;plusmn;&amp;thinsp;0.30 (Kathmandu). The average AE was found to be: 1.25&amp;thinsp;&amp;plusmn;&amp;thinsp;0.24 and 1.26&amp;thinsp;&amp;plusmn;&amp;thinsp;0.18 respectively for two sites. The relation between AOD and AE was used to discriminate the aerosol types over these sites which indicated anthropogenic, mixed and biomass burning origin aerosol constituted the major aerosol types in Lumbini and Kathmandu. A clear bi-modal distribution of aerosol volume size was observed with highest volume concentration during the post-monsoon season in fine mode and pre-monsoon season in coarse mode (Lumbini) and highest value over both modes during pre-monsoon season in Kathmandu. The single scattering albedo (SSA) and asymmetry parameter (AP) analyses suggested aerosols over the Himalayan foothills sites are dominated by absorbing and anthropogenic aerosols from urban and industrial activities and biomass burning. Long-term studies are essential to understand and characterize the nature of aerosol over this research gap zone.


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