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Abstract: Discriminating the absorption coefficients of aerosol mineral dust and black carbon (BC) in different aerosol size fractions is a challenge because of BC's large mass absorption cross-section compared to dust. Ambient aerosol wavelength dependent absorption coefficients in supermicron and submicron size fractions were determined with a high time resolution. The measurements were performed simultaneously using identical systems at an urban and a regional background site in Qatar. At each site, measurements were taken by co-located Aethalometers, one with a virtual impactor (VI) and the other with a PM1 cyclone to respectively collect super-micron-enhanced and submicron fractions. The combined measurement of aerosol absorption and scattering coefficients enabled the particles to be classified based on their optical properties' wavelength dependence. The classification reveals the presence of BC internally/externally mixed with different aerosols. Helium ion microscopy images provided information concerning the extent of mineral dust in the submicron fraction. The determination of absorption coefficients during dust storms and non-dust periods was used to establish the absorption Ångström exponent for dust and BC. Non-parametric wind regression, potential source contribution function and back-trajectory analysis reveal major regional sources of desert dust associated with north-westerly winds and a minor local dust contribution. In contrast, major BC sources found locally were associated with south-westerly winds with a smaller contribution made by offshore emissions transported by north-easterly and easterly winds. The use of a pair of Aethalometers with VI and PM1 inlets separates contributions of BC and dust to the aerosol absorption coefficient.
Keywords: aerosol absorption, black carbon, mineral dust, desert dust, Arabian Peninsula
Published in RUNG: 29.02.2024; Views: 447; Downloads: 5
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Abstract: Abstract. Recent years have seen an increase in the use of wood for energy production of over 30 %, and this trend is expected to continue due to the current energy crisis and geopolitical instability. At present, residential wood burning (RWB) is one of the most important sources of organic aerosols (OA) and black carbon (BC). While BC is recognized for its large light absorption cross-section, the role of OA in light absorption is still under evaluation due to their heterogeneous composition and source-dependent optical properties. Studies that characterize wood-burning aerosol emissions in Europe typically focus on urban and background sites and only cover BC properties. However, RWB is more prevalent in rural areas, and the present scenario indicates that an improved understanding of the RWB aerosol optical properties and their subsequent connection to climate impacts is necessary for rural areas. We have characterized atmospheric aerosol particles from a central European rural site during wintertime in the village of Retje in Loški Potok, Slovenia, from 01.12.2017 to 07.03.2018. The village experienced extremely high aerosol concentrations produced by RWB and near-ground temperature inversion. The isolated location of the site and the substantial local emissions made it an ideal laboratory-like place for characterizing RWB aerosols with low influence from non-RWB sources under ambient conditions. The mean mass concentrations of OA and BC were 34.8 µg m-3 (max = 271.8 µg m-3) and 3.1 µg m-3 (max = 24.3 µg m-3), respectively. The mean total particle number concentration (10–600 nm) was 9.9 x 103 particles cm-3 (max = 53.5 x 103 particles cm-3). The mean total light absorption coefficient at 370 nm and 880 nm measured by an Aethalometer AE33 were 122.8 Mm-1 and 15.3 Mm-1 and had maximum values of 1103.9 Mm-1 and 179.1 Mm-1, respectively. The aerosol concentrations and absorption coefficients measured during the campaign in Loški Potok were significantly larger than those reported values for several urban areas in the region with larger populations and extent of aerosol sources. Here, considerable contributions from brown carbon (BrC) to the total light absorption were identified, reaching up to 60 % and 48 % in the near UV (370 nm) and blue (470 nm) wavelengths. These contributions are up to three times higher than values reported for other sites impacted by wood-burning emissions. The calculated mass absorption cross-section and the absorption Ångström exponent for RWB OA were MACOA, 370 nm= 2.4 m2 g-1, and AAEBrC, 370–590 nm= 3.9, respectively. Simple forcing efficiency (SFE) calculations were performed as a sensitivity analysis to evaluate the climate impact of the RWB aerosols produced at the study site by integrating the optical properties measured during the campaign. The SFE results show a considerable forcing capacity from the local RWB aerosols, with a high sensitivity to OA absorption properties and a more substantial impact over bright surfaces like snow, typical during the coldest season with higher OA emissions from RWB. Our study's results are highly significant regarding air pollution, optical properties, and climate impact. The findings suggest that there may be an underestimation of RWB emissions in rural Europe and that further investigation is necessary.
Keywords: wood-burning aerosols, optical characterization, black carbon, rural areas
Published in RUNG: 10.01.2024; Views: 597; Downloads: 6
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Abstract: Light-absorbing aerosols (LAA) impact the atmosphere by heating it. Their effect in the Arctic was investigated during two summer Arctic oceanographic campaigns (2018 and 2019) around the Svalbard Archipelago in order to unravel the differences between the Arctic background and the local anthropic settlements. Therefore, the LAA heating rate (HR) was experimentally determined. Both the chemical composition and high-resolution measurements highlighted substantial differences between the Arctic Ocean background (average eBC concentration of 11.7 ± 0.1 ng/m3) and the human settlements, among which the most impacting appeared to be Tromsø and Isfjorden (mean eBC of 99.4 ± 3.1 ng/m3). Consequently, the HR in Isfjorden (8.2 × 10−3 ± 0.3 × 10−3 K/day) was one order of magnitude higher than in the pristine background conditions (0.8 × 10−3 ± 0.9 × 10−5 K/day). Therefore, we conclude that the direct climate impact of local LAA sources on the Arctic atmosphere is not negligible and may rise in the future due to ice retreat and enhanced marine traffic.
Keywords: light-absorbing aerosols, black carbon, climate change, heating rate
Published in RUNG: 21.12.2023; Views: 675; Downloads: 5
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Keywords: black carbon, brown carbon, carbonaceous aerosol, wildfire, air quality, CASS
Published in RUNG: 06.06.2023; Views: 1183; Downloads: 10
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Keywords: Aerosol vertical profiles, Black carbon, Nanoparticles, Arctic pollution
Published in RUNG: 12.10.2022; Views: 1350; Downloads: 0
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