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Träfflista för sökning "WFRF:(Hansson Hans Christen) srt2:(2005-2009)"

Sökning: WFRF:(Hansson Hans Christen) > (2005-2009)

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1.
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2.
  • Andersson, Camilla, 1979- (författare)
  • Air Pollution Dependency on Climate Variability and Source Region : Past, Current and Future Air Pollution Scenarios over Europe
  • 2009
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • The main objectives of this thesis were to investigate the dependency of European air pollution on climate variability and emission source region. Calculations with a chemistry transport model (CTM) were conducted to investigate the influence of climate variability. The CTM was forced by both simulated past (a re-analysis spanning 1958-2001) and future (a climate simulation spanning 1961-2100) meteorology keeping anthropogenic emissions constant. To investigate the influence of emission source region emissions were varied in western, eastern and northern Europe in seven-year (1997-2003) simulations. The main conclusions in this thesis are §         There is variability in air pollution due to climate variability on time scales from year to year to decades and long-term trends. Hence, what is measured now will not be valid in a decade, or even next year. §         Interannual variability in air pollution due to climate variability is greater than interannual variability in anthropogenic emissions. §         The extreme conditions in 2003, resulting in elevated surface O3 concentrations, could be an indication on what we can expect in the future. §         The trend in surface O3 over the past due to climate change is similar to the projected trend due to future climate change: increasing in south-western and central Europe and decreasing in north-eastern Europe. §         Changes in isoprene emissions and dry deposition dependency on soil moisture are of importance for changes in surface O3 in central and southern Europe. It is vital to include these processes, especially the latter in climate change effect studies of surface O3. §         This work indicates that it is of greater importance for health benefits of the European population to reduce primary PM emissions than precursors of secondary inorganic aerosol under the assumption of higher relative risk for primary PM. This is especially the case in western Europe.
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3.
  • Dal Maso, Miikka, et al. (författare)
  • Annual and interannual variation in boreal forest aerosol particle number and volume concentration and their connection to particle formation
  • 2008
  • Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:4, s. 495-508
  • Tidskriftsartikel (refereegranskat)abstract
    • We investigated size-resolved submicrometre aerosol particle number and volume concentration time series as well as aerosol dynamic parameters derived front Differential Mobility Particle Sizer (DMPS) measurements at five background stations in the Nordic boreal forest area. The stations in question were Aspvreten, Hyytiala and Uto in Southern Finland and Sweden, and Varrio and Pallas in the Finnish Lapland. The objective Of Our investigation was to identify and quantity annual and interannual variation observable in the time series. We found that the total number and mass concentrations were touch lower at the Lapland stations than at the southern stations and that the total particle number was strongly correlated to particle formation event frequency. The annual total number concentration followed the annual distribution of particle formation events at the Southern stations but much less clearly at the Lapland stations. The volume concentration was highest during summer, in line with higher condensation growth rates: this is in line with the assumption that a large part of the particle volume is produced by oxidized plant emissions. The decrease of sulphate emissions in Europe was not visible in our data set. Aerosol dynamic parameters such as condensation sink, condensation sink diameter and the power law exponent linking coagulation losses and condensation sink are presented to characterize the submicron Nordic background aerosol.
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4.
  • Ekström, Sanna, et al. (författare)
  • First direct measurements of the CCN properties of 2-methyltetrols and polyols
  • 2008
  • Ingår i: Geophysical Research Abstracts.
  • Konferensbidrag (refereegranskat)abstract
    • 2-methyltetrols and polyols have received a lot of attention in recent years. 2-methyltetrols have been found in aerosols in various regions are believed to be formed by the oxidation of isoprene. Polyols are produced by fungi and have been measuredin large concentrations in aerosols. The main reason of interest of both 2-methyltetrols and polyols as efficient cloud condensation nuclei (CCN) is due to their high solubility.This presentation will report for the first time the experimental determination of complete Köhler curves for 2-methyltetrols (2-methylerythritol and 2-methylthreitol), C3 to C6 polyols (glycerol, erythritol, arabitol, and mannitol), and for comparison theiranalogue di-acids (malonic acid, succinic acid and, adipic acid). The original Köhler equations were determined from osmolality and tensiometry measurements of the compounds both in water and salt solutions (sodium chloride and ammonium sulphate).The results indicate that the polyols generally have similar CCN properties as the dicarboxylic acids. The critical supersaturation for aerosol particles with a 30 nm radius were: 2-methyltetrol; 0.68%, mannitol; 0.62%, arabitol; 0.60%, 2-methylerythritol;0.57%, erythritol; 0.56%, glycerol; 0.53%, adipic acid; 0.52%, succinic acid; 0.49%, and malonic acid; 0.44%. Mixtures of salts had lower critical supersaturation than water solutions, especially for the polyols. One exception was 2-methylerythritol, which interestingly was less efficient as CCN in salt solutions.The CCN efficiency of the polyols is believed to result mostly from their large water affinity, enforcing the Raoult effect, while organic acids lower the Kelvin effect. The very large solubility of polyols compared to the di-acids mean that they could positive effect in the initial phase of the droplet growth while the di-acids cannot. 2-methyltetrols were found to have both a Kelvin and a Raoult effect.In addition, these results establish for the first time that the 3-dimensional structure of molecules can have an effect on their CCN properties. The two isomers of the 2-methyltetrols have significantly different CCN properties that are also influencedoppositely in the presence of salts.
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5.
  • Ekström, Sanna, et al. (författare)
  • The Cloud Condensation Nuclei (CCN) properties of 2-methyltetrols and C3-C6 polyols from osmolality and surface tension measurements
  • 2009
  • Ingår i: Atmospheric Chemistry And Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 9:3, s. 973-980
  • Tidskriftsartikel (refereegranskat)abstract
    • A significant fraction of the organic material in aerosols is made of highly soluble compounds such as sugars (mono-and polysaccharides) and polyols such as the 2-methyltetrols, methylerythritol and methyltreitol. Because of their high solubility these compounds are considered as potentially efficient CCN material. For the 2-methyltetrols, this would have important implications for cloud formation at global scale because they are thought to be produced by the atmospheric oxidation of isoprene. To investigate this question, the complete Kohler curves for C3-C6 polyols and the 2-methyltetrols have been determined experimentally from osmolality and surface tension measurements. Contrary to what was expected, none of these compounds displayed a higher CCN efficiency than organic acids. Their Raoult terms show that this limited CCN efficiency is due to their absence of dissociation in water, this in spite of slight surface-tension effects for the 2-methyltetrols. Thus, compounds such as saccharides and polyols would not contribute more to cloud formation than other organic compounds studied so far. In particular, the presence of 2-methyltetrols in aerosols would not particularly enhance cloud formation in the atmosphere, in contrary to recently suggested
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6.
  • Ekström, Sanna, et al. (författare)
  • The Cloud Condensation Nuclei (CCN) properties of 2-methyltetrols and C3–C6 polyols from osmolality and surface tension measurements (Discussion paper)
  • 2008
  • Ingår i: Atmospheric Chemistry and Physics Discussion. - : Copernicus GmbH. - 1680-7367. ; 8:5, s. 17237-17256
  • Tidskriftsartikel (refereegranskat)abstract
    • A significant fraction of the organic material in aerosols is made of highly soluble compounds such as sugars (mono- and polysaccharides) and polyols, including the 2-methyltetrols, methylerythritol and methyltreitol. The high solubility of these compounds has brought the question of their potentially high CCN efficiency. For the 2-methyltetrols, this would have important implications for cloud formation at global scale because they are thought to be produced by the atmospheric oxidation of isoprene. To investigate this question, the complete Köhler curves for C3–C6 polyols and the 2-methyltetrols have been determined experimentally from osmolality and surface tension measurements. Contrary to what expected, none of these compounds displayed a critical supersaturation lower than those of inorganic salts or organic acids. Their Raoult terms show that this limited CCN efficiency is due to their absence of dissociation in water, this in spite of slight surface-tension effects for the 2-methyltetrols. Thus, compounds such as sugars and polyols would not contribute more to cloud formation in the atmosphere than any other organic compounds studied so far. In particular, the presence of 2-methyltetrols in aerosols would not particularly enhance cloud formation in the atmosphere, contrary to what has been suggested.
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7.
  • Hussein, T., et al. (författare)
  • Time span and spatial scale of regional new particle formation events over Finland and Southern Sweden
  • 2009
  • Ingår i: Atmospheric Chemistry And Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 9:14, s. 4699-4716
  • Tidskriftsartikel (refereegranskat)abstract
    • We investigated the time span and spatial scale of regional new particle formation (NPF) events in Finland and Southern Sweden using measured particle number size distributions at five background stations. We define the time span of a NPF event as the time period from the first moment when the newly formed mode of aerosol particles is observable below 25 nm until the newly formed mode is not any more distinguishable from other background modes of aerosol particles after growing to bigger sizes. We identify the spatial scale of regional NPF events based on two independent approaches. The first approach is based on the observation within a network of stationary measurement stations and the second approach is based on the time span and the history of air masses back-trajectories. According to the second approach, about 60% and 28% of the events can be traced to distances longer than 220 km upwind from where the events were observed in Southern Finland (Hyytiälä) and Northern Finland (Värriö), respectively. The analysis also showed that the observed regional NPF events started over the continents but not over the Atlantic Ocean. The first approach showed that although large spatial scale NPF events are frequently observed at several locations simultaneously, they are rarely identical (similar characteristics and temporal variations) due to differences in the initial meteorological and geographical conditions between the stations. The growth of the newly formed particles during large spatial scale events can be followed for more than 30 h where the newly formed aerosol particles end up in the Aitken mode (diameter 25–100 nm) and accumulation mode size ranges (diameter 0.1–1 μm). This study showed clear evidence that regional NPF events can pose a significant source for accumulation mode particles over the Scandinavian continent provided that these findings can be generalized to many of the air masses traveling over the European continent.
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8.
  • Kulmala, Markku, et al. (författare)
  • Overview of the biosphere-aerosol-cloud-climate interactions (BACCI) studies
  • 2008
  • Ingår i: Tellus. Series B: Chemical and Physical Meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:3, s. 300-317
  • Forskningsöversikt (refereegranskat)abstract
    • Here we present research methods and results obtained by the Nordic Centre of Excellence Biosphere-Aerosol-Cloud-Climate Interactions (BACCI) between 1 January 2003 and 31 December 2007. The centre formed an integrated attempt to understand multiple, but interlinked, biosphere-atmosphere interactions applying inter and multidisciplinary approaches in a coherent manner. The main objective was to study the life cycle of aerosol particles and their importance on climate change. The foundation in BACCI was a thorough understanding of physical, meteorological, chemical and ecophysiological processes, providing a unique possibility to study biosphere-aerosol-cloud-climate interactions. Continuous measurements of atmospheric concentrations and fluxes of aerosol particles and precursors and, CO2/aerosol trace gas interactions in different field stations (e.g. SMEAR) were supported by models of particle thermodynamics, transport and dynamics, atmospheric chemistry, boundary layer meteorology and forest growth. The main progress was related to atmospheric new particle formation, existence of clusters, composition of nucleation mode aerosol particles, chemical precursors of fresh aerosol particles, the contribution of biogenic aerosol particles on the global aerosol load, transport, transformation and deposition of aerosol particles, thermodynamics related to aerosol particles and cloud droplets, and the microphysics and chemistry of cloud droplet formation.
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9.
  • Monks, P. S., et al. (författare)
  • Atmospheric composition change : global and regional air quality
  • 2009
  • Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310 .- 1873-2844. ; 43:33, s. 5268-5350
  • Forskningsöversikt (refereegranskat)abstract
    • Air quality transcends all scales with in the atmosphere from the local to the global with handovers and feedbacks at each scale interaction. Air quality has manifold effects on health, ecosystems heritage and, climate. In this review the state of scientific understanding in relation to global and regional air quality is outlined. The review discusses air quality, in terms of emissions, processing and transport of trace gases and aerosols. New insights into the characterization of both natural and anthropogenic emissions are reviewed looking at both natural (e.g. dust and lightning) as well as plant emissions. Trends in anthropogenic emissions both by region and globally are discussed as well as biomass burning emissions. In terms of chemical processing the major air quality elements of ozone, non-methane hydrocarbons, nitrogen oxides and aerosols are covered. A number of topics are presented as a way of integrating the process view into the atmospheric context; these include the atmospheric oxidation efficiency, halogen and HOx chemistry, nighttime chemistry, tropical chemistry, heat waves, megacities, biomass burning and the regional hot spot of the Mediterranean. New findings with respect to the transport of pollutants across the scales are discussed, in particular the move to quantify the impact of long-range transport on regional air quality. Gaps and research questions that remain intractable are identified. The review concludes with a focus of research and policy questions for the coming decade. In particular, the policy challenges for concerted air quality and climate change policy (co-benefit) are discussed.
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