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Abstract: One-year measurements (October 2016–September 2017) of aerosol optical properties in the Athens urban environment were analyzed; for closure purposes, the results were supported by data of chemical composition of the non-refractory submicron aerosol fraction acquired with an Aerosol Chemical Speciation Monitor (ACSM). Both the spectral scattering (bsca) and absorption (babs) coefficients exhibit a pronounced annual variability with higher values (63.6 Mm–1 at 550 nm and 41.0 Mm–1 at 520 nm, respectively) in winter, due to domestic heating releasing increased carbonaceous emissions and the shallow mixing layer trapping aerosols near the surface. Much lower values (33.5 Mm–1 and 22.9 Mm–1 for bsca and babs, respectively) are found during summer, indicating rather aged aerosols from regional sources. The estimations of the dry spectral single scattering albedo (SSA), scattering (SAE) and absorption (AAE) Ångström exponents focus on the seasonality of the urban aerosols. The high SAE (~2.0) and low SSA (0.62 ± 0.11) values throughout the year indicate the dominance of fine-absorbing aerosols from fossil-fuel combustion, while the high AAE (~1.5) in winter suggests enhanced presence of biomass-burning aerosols. Pronounced morning and late evening/night peaks are found in both bsca and babs during winter, coinciding with the morning traffic rush hour and increased residential wood burning in the evening, while in the other seasons, the diurnal patterns flatten out. The wind speed strongly affects the aerosol loading and properties in winter, since for winds below 3 m s–1, a high increase in bsca and babs is observed, consistent with low dilution processes and hazy/smoggy conditions. Our closure experiments indicate a good agreement (R2 = 0.91, slope = 1.08) between the reconstructed and measured bsca values and reveal that organic matter contributes about half of the sub-micron mass in winter, followed by sulfate (~40%) and nitrate (10%, only in winter) aerosols.
Keywords: urban aerosols, light scattering, absorption, chemical species, wood burning, Athens
Published in RUNG: 10.05.2024; Views: 146; Downloads: 2
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Abstract: Abstract. Black carbon (BC) is recognized as the most important warming agent among atmospheric aerosol particles. The absorption efficiency of pure BC is rather well-known, nevertheless the mixing of BC with other aerosol particles can enhance the BC light absorption efficiency, thus directly affecting Earth's radiative balance. The effects on climate of the BC absorption enhancement due to the mixing with these aerosols are not yet well constrained because these effects depend on the availability of material for mixing with BC, thus creating regional variations. Here we present the mass absorption cross-section (MAC) and absorption enhancement of BC particles (Eabs), at different wavelengths (from 370 to 880 nm for online measurements and at 637 nm for offline measurements) measured at two sites in the western Mediterranean, namely Barcelona (BCN; urban background) and Montseny (MSY; regional background). The Eabs values ranged between 1.24 and 1.51 at the urban station, depending on the season and wavelength used as well as on the pure BC MAC used as a reference. The largest contribution to Eabs was due to the internal mixing of BC particles with other aerosol compounds, on average between a 91 % and a 100 % at 370 and 880 nm, respectively. Additionally, 14.5 % and 4.6 % of the total enhancement at the short ultraviolet (UV) wavelength (370 nm) was due to externally mixed brown carbon (BrC) particles during the cold and the warm period, respectively. On average, at the MSY station, a higher Eabs value was observed (1.83 at 637 nm) compared to BCN (1.37 at 637 nm), which was associated with the higher fraction of organic aerosols (OA) available for BC coating at the regional station, as denoted by the higher organic carbon to elemental carbon (OC:EC) ratio observed at MSY compared to BCN. At both BCN and MSY, Eabs showed an exponential increase with the amount of non-refractory (NR) material available for coating (RNR-PM). The Eabs at 637 nm at the MSY regional station reached values up to 3 during episodes with high RNR-PM, whereas in BCN, Eabs kept values lower than 2 due to the lower relative amount of coating materials measured at BCN compared to MSY. The main sources of OA influencing Eabs throughout the year were hydrocarbon OA (HOA) and cooking-related OA (COA), i.e. primary OA (POA) from traffic and cooking emissions, respectively, at both 370 and 880 nm. At the short UV wavelength (370 nm), a strong contribution to Eabs from biomass burning OA (BBOA) and less oxidized oxygenated OA (LO-OOA) sources was observed in the colder period. Moreover, we found an increase of Eabs with the ageing state of the particles, especially during the colder period. This increase of Eabs with particle ageing was associated with a larger relative amount of secondary OA (SOA) compared to POA. The availability of a long dataset at both stations from offline measurements enabled a decade-long trend analysis of Eabs at 637 nm, that showed statistically significant (s.s.) positive trends of Eabs during the warmer months at the MSY station. This s.s. positive trend in MSY mirrored the observed increase of the OC:EC ratio over time. Moreover, in BCN during the COVID-19 lockdown period in spring 2020 we observed a sharp increase of Eabs due to the observed sharp increase of the OC:EC ratio. Our results show similar values of Eabs to those found in the literature for similar background stations.
Keywords: black carbomn, coating, organic aerosol, light absorption
Published in RUNG: 10.05.2024; Views: 126; Downloads: 2
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Abstract: This study examines the spectral properties and source characteristics of absorbing aerosols (BC: Black Carbon; BrC: Brown Carbon, based on aethalometer measurements) in the urban background of Athens during December 2016–February 2017. Using common assumptions regarding the spectral dependence of absorption due to BC (AAEBC = 1) and biomass burning (AAEbb = 2), and calculating an optimal AAEff value for the dataset (1.18), the total spectral absorption was decomposed into five components, corresponding to absorption of BC and BrC from fossil-fuel (ff) combustion and biomass burning (bb), and to secondary BrC estimated using the BC-tracer minimum R-squared (MRS) method. Substantial differences in the contribution of various components to the total absorption were found between day and night, due to differences in emissions and meteorological dynamics, while BrC and biomass burning aerosols presented higher contributions at shorter wavelengths. At 370 nm, the absorption due to BCff contributed 36.3% on average, exhibiting a higher fraction (58.1%) during daytime, while the mean BCbb absorption was estimated at 18.4%. The mean absorption contributions due to BrCff, BrCbb and BrCsec were 6.7%, 32.3% and 4.9%, respectively. The AbsBCff,370 component maximized during the morning traffic hours and was strongly correlated with NOx (R2 = 0.76) and CO (R2 = 0.77), while a similar behavior was seen for the AbsBrCff,370 component. AbsBCbb and AbsBrCbb levels escalated during nighttime and were highly associated with nss-K+ and with the organic aerosol (OA) components related to fresh and fast-oxidized biomass burning (BBOA and SV-OOA) as obtained from ACSM measurements. Multiple linear regression was used to attribute BrC absorption to five OA components and to determine their absorption contributions and efficiencies, revealing maximum contributions of BBOA (33%) and SV-OOA (21%). Sensitivity analysis was performed in view of the methodological uncertainties and supported the reliability of the results, which can have important implications for radiative transfer models.
Keywords: spectral absorption, black carbon, brown carbon, fossil fuel, biomass burning, source apportionment
Published in RUNG: 10.05.2024; Views: 136; Downloads: 0
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Abstract: A preprint of the publication can be found here: AMTD - Response of black carbon and aerosol absorption measuring instruments to laboratory-generated soot coated with controlled amounts of secondary organic matter (copernicus.org) (doi.org/10.5194/amt-2021-214). The files correspond to the raw data sets used for Figures 3 and 4 of the aforementioned publication. The date and start/stop time of the measurements are listed in the file "overview_measurements".
Keywords: aerosol absorption coefficient, black carbon, absorption enhancement
Published in RUNG: 19.03.2024; Views: 446; Downloads: 2
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Abstract: The JATAC campaign in September 2021 and September 2022 on and above Cape Verde Islands resulted in a large in-situ and remote measurement dataset. Its main objective was the calibration and validation of the ESA satellite Aeolus ALADIN Lidar. The campaign also featured secondary scientific objectives related to climate change. Constraining remote sensing measurements with those provided by in-situ instrumentation is crucial for proper characterization and accurate description of the 3-D structure of the atmosphere.We present the results performed with an instrumented light aircraft (Advantic WT-10) set-up for in-situ aerosol measurements. Twenty-seven flights were conducted over the Atlantic Ocean at altitudes around and above 3000 m above sea level during intense dust transport events. Simultaneous measurements with PollyXT, and eVe ground-based lidars took place, determining the vertical profiles of aerosol optical properties, which were also used to plan the flights.The aerosol light extinction coefficient was obtained at three different wavelengths as a combination of the absorption coefficients determined using Continuous Light Absorption Photometers (CLAP) and the scattering coefficients measured with an Ecotech Aurora 4000 nephelometer, which also measured the backscatter fraction. The particle size distributions above 0.3 µm diameter were measured with two Grimm 11-D Optical Particle Size Spectrometers (OPSS). Moreover, CO2 concentration, temperature, aircraft GPS position and altitude, air and ground speed were also measured.We compare the in-situ aircraft measurements of the aerosol extinction coefficients with the AEOLUS lidar derived extinction coefficients, as well as with the ground-based eVe and PollyXT lidar extinction coefficients when measurements overlapped in space and time. The comparison was performed at the closest available wavelengths, with in-situ measurements inter/extrapolated to those of the lidar systems.In general we find an underestimation of the extinction coefficient obtained by lidars compared to the in-situ extinction coefficient. The slopes of regression lines of ground-based lidars, PollyXT and eVe, against the in-situ measurements are characterised by values ranging from 0.61 to 0.7 and R2 between 0.71 and 0.89. Comparison further suggests better agreement between Aeolus ALADIN lidar and the in-situ measurements. Relationship described by fitting the Aeolus to in-situ data is characterised by the slope value 0.76 and R2 of 0.8.The causes of better agreement of the in-situ measurements with the ALADIN lidar than with the surface based ones are being studied, with several reasons being considered: a) lower spatial and temporal resolution which homogenize the area of study in comparison with the very fine vertical variations of the aerosols, which can be detected with the surface-based measurements, impairing the comparison with highly vertically resolved ground-lidar measurements while not affecting averaged space-borne lidar; b) the effect of lower clouds/ Saharan air layers on the attenuation of the lidar signal.The presented results show the importance of the comparison of the remote with in-situ measurements for the support of the research on evolution, dynamics, and predictability of tropical weather systems and provide input into and verification of the climate models.
Keywords: LIDAR, Aeolus, ALADIN, in-situ measurements, aerosol absorption, aerosol extinction, airborne measurements
Published in RUNG: 18.03.2024; Views: 421; Downloads: 6
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