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Träfflista för sökning "WFRF:(Sporre Moa) srt2:(2020-2024)"

Sökning: WFRF:(Sporre Moa) > (2020-2024)

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1.
  • Ausmeel, Stina, et al. (författare)
  • Ship plumes in the Baltic Sea Sulfur Emission Control Area: chemical characterization and contribution to coastal aerosol concentrations
  • 2020
  • Ingår i: Atmospheric Chemistry and Physics. - : Copernicus GmbH. - 1680-7324. ; 20:15, s. 9135-9151
  • Tidskriftsartikel (refereegranskat)abstract
    • In coastal areas, there is increased concern aboutemissions from shipping activities and the associated impacton air quality. We have assessed the ship aerosol propertiesand the contribution to coastal particulate matter (PM) andnitrogen dioxide (NO2) levels by measuring ship plumes inambient conditions at a site in southern Sweden, within a SulfurEmission Control Area. Measurements took place duringa summer and a winter campaign, 10 km downwind ofa major shipping lane. Individual ships showed large variabilityin contribution to total particle mass, organics, sulfate,and NO2. The average emission contribution of theshipping lane was 2913 and 3720 ngm?3 to PM0:5,188 and 3419 ngm?3 to PM0:15, and 1:210:57 and1:110:61 μgm?3 to NO2, during winter and summer, respectively.Sulfate and organics dominated the particle massand most plumes contained undetectable amounts of equivalentblack carbon (eBC). The average eBC contribution was3:51:7 ngm?3 and the absorption Ångström exponent wasclose to 1. Simulated ageing of the ship aerosols using anoxidation flow reactor showed that on a few occasions, therewas an increase in sulfate and organic mass after photochemicalprocessing of the plumes. However, most plumes did notproduce measurable amounts of secondary PM upon simulatedageing.
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  • Blichner, Sara M., et al. (författare)
  • Implementing a sectional scheme for early aerosol growth from new particle formation in the Norwegian Earth System Model v2 : Comparison to observations and climate impacts
  • 2021
  • Ingår i: Geoscientific Model Development. - : Copernicus GmbH. - 1991-959X .- 1991-9603. ; 14:6, s. 3335-3359
  • Tidskriftsartikel (refereegranskat)abstract
    • Aerosol-cloud interactions contribute to a large portion of the spread in estimates of climate forcing, climate sensitivity and future projections. An important part of this uncertainty is how much new particle formation (NPF) contributes to cloud condensation nuclei (CCN) and, furthermore, how this changes with changes in anthropogenic emissions. Incorporating NPF and early growth in Earth system models (ESMs) is, however, challenging due to uncertain parameters (e.g. participating vapours), structural issues (numerical description of growth from ∼ 1 to ∼ 100 nm) and the large scale of an ESM grid compared to the NPF scale. A common approach in ESMs is to represent the particle size distribution by a certain number of log-normal modes. Sectional schemes, on the other hand, in which the size distribution is represented by bins, are considered closer to first principles because they do not make an a priori assumption about the size distribution. In order to improve the representation of early growth, we have implemented a sectional scheme for the smallest particles (5-39.6 nm diameter) in the Norwegian Earth System Model (NorESM), feeding particles into the original aerosol scheme. This is, to our knowledge, the first time such an approach has been tried. We find that including the sectional scheme for early growth improves the aerosol number concentration in the model when comparing against observations, particularly in the 50-100 nm diameter range. Furthermore, we find that the model with the sectional scheme produces much fewer particles than the original scheme in polluted regions, while it produces more in remote regions and the free troposphere, indicating a potential impact on the estimated aerosol forcing. Finally, we analyse the effect on cloud-aerosol interactions and find that the effect of changes in NPF efficiency on clouds is highly heterogeneous in space. While in remote regions, more efficient NPF leads to higher cloud droplet number concentration (CDNC), in polluted regions the opposite is in fact the case.
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  • Blichner, Sara M., 1989-, et al. (författare)
  • Process-evaluation of forest aerosol-cloud-climate feedback shows clear evidence from observations and large uncertainty in models
  • 2024
  • Ingår i: Nature Communications. - 2041-1723. ; 15
  • Tidskriftsartikel (refereegranskat)abstract
    • Natural aerosol feedbacks are expected to become more important in the future, as anthropogenic aerosol emissions decrease due to air quality policy. One such feedback is initiated by the increase in biogenic volatile organic compound (BVOC) emissions with higher temperatures, leading to higher secondary organic aerosol (SOA) production and a cooling of the surface via impacts on cloud radiative properties. Motivated by the considerable spread in feedback strength in Earth System Models (ESMs), we here use two long-term observational datasets from boreal and tropical forests, together with satellite data, for a process-based evaluation of the BVOC-aerosol-cloud feedback in four ESMs. The model evaluation shows that the weakest modelled feedback estimates can likely be excluded, but highlights compensating errors making it difficult to draw conclusions of the strongest estimates. Overall, the method of evaluating along process chains shows promise in pin-pointing sources of uncertainty and constraining modelled aerosol feedbacks.
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5.
  • Blichner, Sara Marie, et al. (författare)
  • Reduced effective radiative forcing from cloud-aerosol interactions (ERFaci) with improved treatment of early aerosol growth in an Earth system model
  • 2021
  • Ingår i: Atmospheric Chemistry and Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 21:23, s. 17243-17265
  • Tidskriftsartikel (refereegranskat)abstract
    • Historically, aerosols of anthropogenic origin have offset some of the warming from increased atmospheric greenhouse gas concentrations. The strength of this negative aerosol forcing, however, is highly uncertain-especially the part originating from cloud-aerosol interactions. An important part of this uncertainty originates from our lack of knowledge about pre-industrial aerosols and how many of these would have acted as cloud condensation nuclei (CCN). In order to simulate CCN concentrations in models, we must adequately model secondary aerosols, including new particle formation (NPF) and early growth, which contributes a large part of atmospheric CCN. In this study, we investigate the effective radiative forcing (ERF) from cloud-aerosol interactions (ERFaci) with an improved treatment of early particle growth, as presented in . We compare the improved scheme to the default scheme, OsloAero, which are both embedded in the atmospheric component of the Norwegian Earth System Model v2 (NorESM2). The improved scheme, OsloAeroSec, includes a sectional scheme that treats the growth of particles from 5-39.6ĝ€¯nm in diameter, which thereafter inputs the particles to the smallest mode in the pre-existing modal aerosol scheme. The default scheme parameterizes the growth of particles from nucleation up to the smallest mode, a process that can take several hours. The explicit treatment of early growth in OsloAeroSec, on the other hand, captures the changes in atmospheric conditions during this growth time in terms of air mass mixing, transport, and condensation and coagulation. We find that the ERFaci with the sectional scheme is-1.16ĝ€¯Wm-2, which is 0.13ĝ€¯Wm-2 weaker compared to the default scheme. This reduction originates from OsloAeroSec producing more particles than the default scheme in pristine, low-aerosol-concentration areas and fewer NPF particles in high-aerosol areas. We find, perhaps surprisingly, that NPF inhibits cloud droplet activation in polluted and/or high-aerosol-concentration regions because the NPF particles increase the condensation sink and reduce the growth of the larger particles which may otherwise activate. This means that in these high-aerosol regions, the model with the lowest NPF-OsloAeroSec-will have the highest cloud droplet activation and thus more reflective clouds. In pristine and/or low-aerosol regions, however, NPF enhances cloud droplet activation because the NPF particles themselves tend to activate. Lastly, we find that sulfate emissions in the present-day simulations increase the hygroscopicity of secondary aerosols compared to pre-industrial simulations. This makes NPF particles more relevant for cloud droplet activation in the present day than the pre-industrial atmosphere because increased hygroscopicity means they can activate at smaller sizes.
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6.
  • Chen, Deliang, 1961, et al. (författare)
  • Summary of a workshop on extreme weather events in a warming world organized by the Royal Swedish Academy of Sciences
  • 2020
  • Ingår i: Tellus Series B-Chemical and Physical Meteorology. - : Stockholm University Press. - 1600-0889 .- 0280-6509. ; 72:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Climate change is not only about changes in means of climatic variables such as temperature, precipitation and wind, but also their extreme values which are of critical importance to human society and ecosystems. To inspire the Swedish climate research community and to promote assessments of international research on past and future changes in extreme weather events against the global climate change background, the Earth Science Class of the Royal Swedish Academy of Sciences organized a workshop entitled 'Extreme weather events in a warming world' in 2019. This article summarizes and synthesizes the key points from the presentations and discussions of the workshop on changes in floods, droughts, heat waves, as well as on tropical cyclones and extratropical storms. In addition to reviewing past achievements in these research fields and identifying research gaps with a focus on Sweden, future challenges and opportunities for the Swedish climate research community are highlighted.
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  • Martinsson, Bengt G., et al. (författare)
  • Five-satellite-sensor study of the rapid decline of wildfire smoke in the stratosphere
  • 2022
  • Ingår i: Atmospheric Chemistry and Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 22:6, s. 3967-3984
  • Tidskriftsartikel (refereegranskat)abstract
    • Smoke from western North American wildfires reached the stratosphere in large amounts in August 2017. Limb-oriented satellite-based sensors are commonly used for studies of wildfire aerosol injected into the stratosphere (OMPS-LP (Ozone Mapping and Profiler Suite Limb Profiler) and SAGE III/ISS (Stratospheric Aerosol and Gas Experiment III on the International Space Station)). We find that these methods are inadequate for studies of the first 1-2 months after such a strong fire event due to event termination ("saturation"). The nadir-viewing lidar CALIOP (Cloud-Aerosol LIdar with Orthogonal Polarization) is less affected due to shorter path in the smoke; furthermore, it provides a means to develop a method to correct for strong attenuation of the signal. After the initial phase, the aerosol optical depth (AOD) from OMPS-LP and CALIOP show very good agreement above the 380ĝK isentrope, whereas OMPS-LP tends to produce higher AOD than CALIOP in the lowermost stratosphere (LMS), probably due to reduced sensitivity at altitudes below 17ĝkm. Time series from CALIOP of attenuation-corrected stratospheric AOD of wildfire smoke show an exponential decline during the first month after the fire, which coincides with highly significant changes in the wildfire aerosol optical properties. The AOD decline is verified by the evolution of the smoke layer composition, comparing the aerosol scattering ratio (CALIOP) to the water vapor concentration from MLS (Microwave Limb Sounder). Initially the stratospheric wildfire smoke AOD is comparable with the most important volcanic eruptions during the last 25 years. Wildfire aerosol declines much faster, 80ĝ%-90ĝ% of the AOD is removed with a half-life of approximately 10ĝd. We hypothesize that this dramatic decline is caused by photolytic loss. This process is rarely observed in the atmosphere. However, in the stratosphere this process can be studied with practically no influence from wet deposition, in contrast to the troposphere where this is the main removal path of submicron aerosol particles. Despite the loss, the aerosol particles from wildfire smoke in the stratosphere are relevant for the climate.
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9.
  • Martinsson, Johan, et al. (författare)
  • On the Relationship of Biogenic Primary and Secondary Organic Aerosol Tracer Compounds on the Aethalometer Model Parameters
  • 2020
  • Ingår i: Aerosol and Air Quality Research. - : Taiwan Association for Aerosol Research. - 2071-1409 .- 1680-8584. ; 20:12, s. 2654-2668
  • Tidskriftsartikel (refereegranskat)abstract
    • The aethalometer model has shown to offer a fast, inexpensive and robust method for source apportionment. The method relies on aerosol light absorption attribution, mass balance of the total carbon and results in a fraction of unaccounted, residual carbon that has been associated to biogenic carbon due to its presumably non-light absorbing properties. This residual carbon and its relation to tracers of biogenic primary and secondary organic aerosol was investigated at a rural measurement station in Sweden. Special focus is devoted to 3-methyl-1,2,3-butanetricarboxylic acid (MBTCA), a second-generation oxidation compound in biogenic secondary organic aerosols. The results show that the residual carbon and the biogenic tracers show a high degree of correlation and that the tracers were highly seasonally dependent with largest carbon contributions during summer. MBTCA showed positive correlation with the aethalometer model derived absorption coefficients from fossil fuel carbonaceous aerosol, stressing the suspicion that biogenic aerosol might be falsely apportioned to fossil fuel carbon in the aethalometer model. MBTCA showed an increasing degree of correlation with higher aethalometer absorption coefficient wavelengths. However, spectrophotometric analysis revealed that the ambient concentrations of MBTCA are most likely to low to give a significant response in the aethalometer. These results support the application of MBTCA as a molecular tracer for biogenic secondary organic aerosol and indicates that a large fraction of the aethalometer model residual carbon is of biogenic origin. Future studies should investigate the light absorbing properties of precursor monoterpenes such as α-pinene, their oxidation products and eventual influence on the aethalometer model.
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