| 1. |
- Holzinger, R., et al.
(författare)
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A signature of aged biogenic compounds detected from airborne VOC measurements in the high arctic atmosphere in March/April 2018
- 2023
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Ingår i: Atmospheric Environment. - 1352-2310. ; 309
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Tidskriftsartikel (refereegranskat)abstract
- During the PAMARCMiP 2018 campaign (March and April 2018) a proton-transfer-reaction mass spectrometer (PTR-MS) was deployed onboard the POLAR 5 research aircraft and sampled the high Arctic atmosphere under Arctic haze conditions. More than 100 compounds exhibited levels above 1 pmol/mol in at least 25% of the measurements. We used acetone mixing ratios, ozone concentrations, and back trajectories to identify periods with and without long-range transport from continental sources. During two flights, surface ozone depletion events (ODE) were observed that coincided with enhanced levels of acetone, and methylethylketone, and ice nucleating particles (INP).Air masses with continental influence contained elevated levels of compounds associated with aged biogenic emissions and anthropogenic pollution (e.g., methanol, peroxyacetylnitrate (PAN), acetone, acetic acid, meth-ylethylketone (MEK), proprionic acid, and pentanone). Almost half of all positively detected compounds (>100) in the high Arctic atmosphere can be associated with terpene oxidation products, likely produced from mono-terpenes and sesquiterpenes emitted from boreal forests. We speculate that the transport of biogenic terpene emissions may constitute an important control of the High Arctic aerosol burden. The sum concentration of the detected aerosol forming vapours is-12 pmol/mol, which is of the same order than measured dimethylsulfide (DMS) mixing ratios and their mass density corresponds to approximately one fifth of the measured non-black -carbon particles.
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| 2. |
- Sinha, P. R., et al.
(författare)
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Evaluation of ground-based black carbon measurements by filter-based photometers at two Arctic sites
- 2017
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Ingår i: Journal of Geophysical Research - Atmospheres. - 2169-897X .- 2169-8996. ; 122:6, s. 3544-3572
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Tidskriftsartikel (refereegranskat)abstract
- Long-term measurements of the light absorption coefficient (b(abs)) obtained with a particle soot absorption photometer (PSAP), b(abs) (PSAP), have been previously reported for Barrow, Alaska, and Ny-angstrom lesund, Spitsbergen, in the Arctic. However, the effects on b(abs) of other aerosol chemical species coexisting with black carbon (BC) have not been critically evaluated. Furthermore, different mass absorption cross section (MAC) values have been used to convert b(abs) to BC mass concentration (M-BC=b(abs)/MAC). We used a continuous soot monitoring system (COSMOS), which uses a heated inlet to remove volatile aerosol compounds, to measure b(abs) (b(abs) (COSMOS)) at these sites during 2012-2015. Field measurements and laboratory experiments have suggested that b(abs) (COSMOS) is affected by about 9% on average by sea-salt aerosols. M-BC values derived by COSMOS (M-BC (COSMOS)) using a MAC value obtained by our previous studies agreed to within 9% with elemental carbon concentrations at Barrow measured over 11months. b(abs) (PSAP) was higher than b(abs) (COSMOS), by 22% at Barrow (PM1) and by 43% at Ny-angstrom lesund (PM10), presumably due to the contribution of volatile aerosol species to b(abs) (PSAP). Using b(abs) (COSMOS) as a reference, we derived M-BC (PSAP) from b(abs) (PSAP) measured since 1998. We also established the seasonal variations of M-BC at these sites. Seasonally averaged M-BC (PSAP) decreased at a rate of about 0.550.30ngm(-3)yr(-1). We also compared M-BC (COSMOS) and scaled M-BC (PSAP) values with previously reported data and evaluated the degree of inconsistency in the previous data.
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