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Träfflista för sökning "WFRF:(Andersson August) ;spr:eng"

Sökning: WFRF:(Andersson August) > Engelska

  • Resultat 1-10 av 104
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1.
  • Horst, Axel, et al. (författare)
  • Compound-specific bromine isotope analysis of methyl bromide using gas chromatography hyphenated with inductively coupled plasma multiple-collector mass spectrometry
  • 2011
  • Ingår i: Rapid Communications in Mass Spectrometry. - : Wiley. - 0951-4198 .- 1097-0231. ; 25:17, s. 2425-2432
  • Tidskriftsartikel (refereegranskat)abstract
    • Methyl bromide is the most important natural bromine contributor to stratospheric ozone depletion, yet there are still large uncertainties regarding quantification of its sources and sinks. The stable bromine isotope composition of CH(3)Br is potentially a powerful tool to apportion its sources and to study both its transport and its reactive fate. A novel compound-specific method to measure (81)Br/(79)Br isotope ratios in CH3Br using gas chromatography hyphenated with inductively coupled plasma multiple-collector mass spectrometry (GC/MCICPMS) was developed. Sample amounts of >40 ng could bemeasured with a precision of 0.1 parts per thousand (1 sigma, n=3). The method results are reproducible over the long term as shown with 36 analyses acquired over 3 months, yielding a standard deviation ( 1s) better than 0.4 parts per thousand. This new method demonstrates for the first time Br isotope ratio determination in gaseous brominated samples. It is three orders of magnitude more sensitive than previously existing isotope ratio mass spectrometry methods for Br isotope determination of other organobromines, thus allowing applications towards ambient atmospheric samples.
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2.
  • Abreu, P, et al. (författare)
  • Measurement of the strange quark forward-backward asymmetry around the Z(0) peak
  • 2000
  • Ingår i: EUROPEAN PHYSICAL JOURNAL C. - : SPRINGER VERLAG. - 1434-6044. ; 14:4, s. 613-631
  • Tidskriftsartikel (refereegranskat)abstract
    • A precise measurement of the strange quark forward-backward asymmetry used 3.2 M multihadronic events around the Z(0) peak collected by the DELPHI experiment from 1992 to 1995. The ring imaging Cherenkov detectors in the barrel and end-cap regions identif
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3.
  • Andersson, August, et al. (författare)
  • (14)C-Based source assessment of soot aerosols in Stockholm and the Swedish EMEP-Aspvreten regional background site
  • 2011
  • Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310 .- 1873-2844. ; 45:1, s. 215-222
  • Tidskriftsartikel (refereegranskat)abstract
    • Combustion-derived soot or black carbon (BC) in the atmosphere has a strong influence on both climate and human health. In order to propose effective mitigation strategies for BC emissions it is of importance to investigate geographical distributions and seasonal variations of BC emission sources. Here, a radiocarbon methodology is used to distinguish between fossil fuel and biomass burning sources of soot carbon (SC). SC is isolated for subsequent off-line (14)C quantification with the chemothermal oxidation method at 375 degrees C (CTO-375 method), which reflects a recalcitrant portion of the BC continuum known to minimize inadvertent inclusion of any non-pyrogenic organic matter. Monitored wind directions largely excluded impact from the Stockholm metropolitan region at the EMEP-Aspvreten rural station 70 km to the south-west. Nevertheless, the Stockholm city and the rural stations yielded similar relative source contributions with fraction biomass (f(biomass)) for fall and winter periods in the range of one-third to half. Large temporal variations in (14)C-based source apportionment was noted for both the 6 week fall and the 4 month winter observations. The f(biomass) appeared to be related to the SC concentration suggesting that periods of elevated BC levels may be caused by increased wood fuel combustion. These results for the largest metropolitan area in Scandinavia combine with other recent (14)C-based studies of combustion-derived aerosol fractions to suggest that biofuel combustion is contributing a large portion of the BC load to the northern European atmosphere.
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4.
  • Andersson, August (författare)
  • A Model for the Spectral Dependence of Aerosol Sunlight Absorption
  • 2017
  • Ingår i: ACS Earth and Space Chemistry. - : American Chemical Society (ACS). - 2472-3452. ; 1:9, s. 533-539
  • Tidskriftsartikel (refereegranskat)abstract
    • Sunlight-absorbing aerosols, e.g., black and brown carbon (BC and BrC), have a potentially large, but highly uncertain contribution to climate warming. The spectral dependence of the aerosol absorption in the visible and near-UV regime is almost universally well-described with a heuristic power law, where the exponent is termed the absorption Angstrom exponent. However, the 2 underlying physicochemical causes for this relation are unknown. Here, a model is presented that predicts the emergence of the power law spectral dependence and unifies the absorption behavior of BC and BrC. Building on the theory of light absorption in amorphous materials, the interaction between multiple functional groups upon absorption is predicted to be a key feature for this broad spectral dependence. This aerosol amorphous absorption model is in agreement with recent empirical findings and provides a conceptual basis for the additional research needed to better constrain the optical properties of light-absorbing aerosols and their environmental impact.
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5.
  • Andersson, August (författare)
  • A systematic examination of a random sampling strategy for source apportionment calculations
  • 2011
  • Ingår i: Science of the Total Environment. - : Elsevier BV. - 0048-9697 .- 1879-1026. ; 412, s. 232-238
  • Tidskriftsartikel (refereegranskat)abstract
    • Estimating the relative contributions from multiple potential sources of a specific component in a mixed environmental matrix is a general challenge in diverse fields such as atmospheric, environmental and earth sciences. Perhaps the most common strategy for tackling such problems is by setting up a system of linear equations for the fractional influence of different sources. Even though an algebraic solution of this approach is possible for the common situation with N + 1 sources and N source markers, such methodology introduces a bias, since it is implicitly assumed that the calculated fractions and the corresponding uncertainties are independent of the variability of the source distributions. Here, a random sampling (RS) strategy for accounting for such statistical bias is examined by investigating rationally designed synthetic data sets. This random sampling methodology is found to be robust and accurate with respect to reproducibility and predictability. This method is also compared to a numerical integration solution for a two-source situation where source variability also is included. A general observation from this examination is that the variability of the source profiles not only affects the calculated precision but also the mean/median source contributions.
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6.
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7.
  • Andersson, August, et al. (författare)
  • Magnetic resonance investigations of lipid motion in isotropic bicelles
  • 2005
  • Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 21:7, s. 7702-7709
  • Tidskriftsartikel (refereegranskat)abstract
    • The dynamics of DMPC in different isotropic bicelles have been investigated by NMR and EPR methods. The local dynamics were obtained by interpretation of 13C NMR relaxation measurements of DMPC in the bicelles, and these results were compared to EPR spectra of spin-labeled lipids. The overall size of the bicelles was investigated by PFG NMR translational diffusion measurements. The dynamics and relative sizes were compared among three different bicelles: [DMPC]/[DHPC] = 0.25, [DMPC]/[DHPC] = 0.5, and [DMPC]/[CHAPS] = 0.5. The local motion is found to depend much more strongly on the choice of the detergent, rather than the overall size of the bicelle. The results provide an explanation for differences in apparent dynamics for different peptides, which are bound to bicelles. This in turn determines under what conditions reasonable NMR spectra can be observed. A model is presented in which extensive local motion, in conjunction with the overall size, affects the spectral properties. An analytical expression for the size dependence of the bicelles, relating the radius of the bilayer region with physical properties of the detergent and the lipid, is also presented.
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8.
  • Andersson, August (författare)
  • Mechanisms for log normal concentration distributions in the environment
  • 2021
  • Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 11:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Log normal-like concentration distributions are ubiquitously observed in the environment. However, the mechanistic origins are not well understood. In this paper, we show that first order exponential kinetics onsets log-normal concentration distributions, under certain assumptions. Given the ubiquity of exponential kinetics, e.g., source and sink processes, this model suggests an explanation for the frequent observation in the environment, and elsewhere. We compare this model to other mechanisms affecting concentration distributions, e.g., source mixing. Finally, we discuss possible implications for data analysis and modelling, e.g., log-normal rates and fluxes.
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9.
  • Andersson, August, et al. (författare)
  • Regionally-Varying Combustion Sources of the January 2013 Severe Haze Events over Eastern China
  • 2015
  • Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 49:4, s. 2038-2043
  • Tidskriftsartikel (refereegranskat)abstract
    • Thick haze plagued northeastern China in January 2013, strongly affecting both regional climate and human respiratory health. Here, we present dual carbon isotope constrained (Delta C-14 and delta C-13) source apportionment for combustion-derived black carbon aerosol (BC) for three key hotspot regions (megacities): North China Plain (NCP, Beijing), the Yangtze River Delta (YRD, Shanghai), and the Pearl River Delta (PRD, Guangzhou) for January 2013. BC, here quantified as elemental carbon (EC), is one of the most health-detrimental components of PM2.5 and a strong climate warming agent. The results show that these severe haze events were equally affected (similar to 30%) by biomass combustion in all three regions, whereas the sources of the dominant fossil fuel component was dramatically different between north and south. In the NCP region, coal combustion accounted for 66% (46-74%, 95% C.I.) of the EC, whereas, in the YRD and PRD regions, liquid fossil fuel combustion (e.g., traffic) stood for 46% (18-66%) and 58% (38-68%), respectively. Taken together, these findings suggest the need for a regionally-specific description of BC sources in climate models and regionally-tailored mitigation to combat severe air pollution events in East Asia.
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10.
  • Andersson, August, et al. (författare)
  • Seasonal source variability of carbonaceous aerosols at the Rwanda Climate Observatory
  • 2020
  • Ingår i: Atmospheric Chemistry And Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 20:8, s. 4561-4573
  • Tidskriftsartikel (refereegranskat)abstract
    • Sub-Saharan Africa (SSA) is a global hot spot for aerosol emissions, which affect the regional climate and air quality. In this paper, we use ground-based observations to address the large uncertainties in the source-resolved emission estimation of carbonaceous aerosols. Ambient fine fraction aerosol was collected on filters at the high-altitude (2590 m a.s.1.) Rwanda Climate Observatory (RCO), a SSA background site, during the dry and wet seasons in 2014 and 2015. The concentrations of both the carbonaceous and inorganic ion components show a strong seasonal cycle, with highly elevated concentrations during the dry season. Source marker ratios, including carbon isotopes, show that the wet and dry seasons have distinct aerosol compositions. The dry season is characterized by elevated amounts of biomass burning products, which approach similar to 95 % for carbonaceous aerosols. An isotopic mass-balance estimate shows that the amount of the carbonaceous aerosol stemming from savanna fires may increase from 0.2 mu g m(-3) in the wet season up to 10 mu g m(-3) during the dry season. Based on these results, we quantitatively show that savanna fire is the key modulator of the seasonal aerosol composition variability at the RCO.
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