| 1. |
- Engvall, Ann-Christine, et al.
(författare)
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In-situ airborne observations of the microphysical properties of the Arctic tropospheric aerosol during late spring and summer
- 2008
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Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:3, s. 392-404
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Tidskriftsartikel (refereegranskat)abstract
- In-situ aerosol data collected in the Arctic troposphere during a three-week period in 2004 were analysed. The measurements took place during late spring, i.e., at the time of the year when the characteristics of the aerosol distribution change from being accumulation-mode dominated to being primarily of the Aitken-mode type, a process that previously has been observed in the boundary layer. To address the question whether this transition is also detectable in the free troposphere of an aircraft-measured data from the ASTAR 2004 campaign were analysed. In this study, we present vertically as well as temporally results from both ground-based and airborne measurements of the total number concentrations of particles larger than 10 and 260 nm. Aircraft-measured size distributions of the aerosol ranging from 20 to 2200 nm have been evaluated with regard to conditions in the boundary layer as well as in the free troposphere. Furthermore an analysis of the volatile fraction of the aerosol population has been performed both for the integrated and size-distributed results. From these investigations we find that the transition takes place in the entire troposphere.
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| 2. |
- Boyer, Matthew, et al.
(författare)
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A full year of aerosol size distribution data from the central Arctic under an extreme positive Arctic Oscillation : insights from the Multidisciplinarydrifting Observatory for the Study of Arctic Climate (MOSAiC) expedition
- 2023
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Ingår i: Atmospheric Chemistry And Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 23:1, s. 389-415
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Tidskriftsartikel (refereegranskat)abstract
- The Arctic environment is rapidly changing due to accelerated warming in the region. The warming trend is driving a decline in sea ice extent, which thereby enhances feedback loops in the surface energy budget in the Arctic. Arctic aerosols play an important role in the radiative balance and hence the climate response in the region, yet direct observations of aerosols over the Arctic Ocean are limited. In this study, we investigate the annual cycle in the aerosol particle number size distribution (PNSD), particle number concentration (PNC), and black carbon (BC) mass concentration in the central Arctic during the Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition. This is the first continuous, year-long data set of aerosol PNSD ever collected over the sea ice in the central Arctic Ocean. We use a k-means cluster analysis, FLEXPART simulations, and inverse modeling to evaluate seasonal patterns and the influence of different source regions on the Arctic aerosol population. Furthermore, we compare the aerosol observations to land-based sites across the Arctic, using both long-term measurements and observations during the year of the MOSAiC expedition (2019–2020), to investigate interannual variability and to give context to the aerosol characteristics from within the central Arctic. Our analysis identifies that, overall, the central Arctic exhibits typical seasonal patterns of aerosols, including anthropogenic influence from Arctic haze in winter and secondary aerosol processes in summer. The seasonal pattern corresponds to the global radiation, surface air temperature, and timing of sea ice melting/freezing, which drive changes in transport patterns and secondary aerosol processes. In winter, the Norilsk region in Russia/Siberia was the dominant source of Arctic haze signals in the PNSD and BC observations, which contributed to higher accumulation-mode PNC and BC mass concentrations in the central Arctic than at land-based observatories. We also show that the wintertime Arctic Oscillation (AO) phenomenon, which was reported to achieve a record-breaking positive phase during January–March 2020, explains the unusual timing and magnitude of Arctic haze across the Arctic region compared to longer-term observations. In summer, the aerosol PNCs of the nucleation and Aitken modes are enhanced; however, concentrations were notably lower in the central Arctic over the ice pack than at land-based sites further south. The analysis presented herein provides a current snapshot of Arctic aerosol processes in an environment that is characterized by rapid changes, which will be crucial for improving climate model predictions, understanding linkages between different environmental processes, and investigating the impacts of climate change in future Arctic aerosol studies.
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| 3. |
- Eckhardt, Sabine, et al.
(författare)
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Revised historical Northern Hemisphere black carbon emissions based on inverse modeling of ice core records
- 2023
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Ingår i: Nature Communications. - : Springer Nature. - 2041-1723. ; 14:1
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Tidskriftsartikel (refereegranskat)abstract
- Black carbon emitted by incomplete combustion of fossil fuels and biomasshas a net warming effect in the atmosphere and reduces the albedo whendeposited on ice and snow; accurate knowledge of past emissions is essentialto quantify and model associated global climate forcing. Although bottom-upinventories provide historical Black Carbon emission estimates that are widelyused in Earth System Models, they are poorly constrained by observationsprior to the late 20th century. Here we use an objective inversion techniquebased on detailed atmospheric transport and deposition modeling to reconstruct1850 to 2000 emissions from thirteen Northern Hemisphere ice-corerecords. We find substantial discrepancies between reconstructed Black Carbonemissions and existing bottom-up inventories which do not fully capturethe complex spatial-temporal emission patterns. Our findings imply changesto existing historical Black Carbon radiative forcing estimates are necessary,with potential implications for observation-constrained climate sensitivity.
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| 4. |
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| 5. |
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| 6. |
- Brioude, Jerome, et al.
(författare)
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The Lagrangian particle dispersion model FLEXPART-WRF version 3.1
- 2013
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Ingår i: Geoscientific Model Development. - : Copernicus GmbH. - 1991-959X .- 1991-9603. ; 6:6, s. 1889-1904
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Tidskriftsartikel (refereegranskat)abstract
- The Lagrangian particle dispersion model FLEXPART was originally designed for calculating long-range and mesoscale dispersion of air pollutants from point sources, such that occurring after an accident in a nuclear power plant. In the meantime, FLEXPART has evolved into a comprehensive tool for atmospheric transport modeling and analysis at different scales. A need for further multiscale modeling and analysis has encouraged new developments in FLEXPART. In this paper, we present a FLEXPART version that works with the Weather Research and Forecasting (WRF) mesoscale meteorological model. We explain how to run this new model and present special options and features that differ from those of the preceding versions. For instance, a novel turbulence scheme for the convective boundary layer has been included that considers both the skewness of turbulence in the vertical velocity as well as the vertical gradient in the air density. To our knowledge, FLEXPART is the first model for which such a scheme has been developed. On a more technical level, FLEXPART-WRF now offers effective parallelization, and details on computational performance are presented here. FLEXPART-WRF output can either be in binary or Network Common Data Form (NetCDF) format, both of which have efficient data compression. In addition, test case data and the source code are provided to the reader as a Supplement. This material and future developments will be accessible at http://www.flexpart.eu.
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| 7. |
- Dasari, Sanjeev, et al.
(författare)
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Source Quantification of South Asian Black Carbon Aerosols with Isotopes and Modeling
- 2020
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Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 54:19, s. 11771-11779
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Tidskriftsartikel (refereegranskat)abstract
- Black carbon (BC) aerosols perturb climate and impoverish air quality/ human health-affecting similar to 1.5 billion people in South Asia. However, the lack of source-diagnostic observations of BC is hindering the evaluation of uncertain bottom-up emission inventories (EIs) and thereby also models/policies. Here, we present dual-isotope-based (Delta C-14/delta C-13) fingerprinting of wintertime BC at two receptor sites of the continental outflow. Our results show a remarkable similarity in contributions of biomass and fossil combustion, both from the site capturing the highly populated highly polluted Indo-Gangetic Plain footprint (IGP; Delta C-14-f(biomass) = 50 +/- 3%) and the second site in the N. Indian Ocean representing a wider South Asian footprint (52 +/- 6%). Yet, both sites reflect distinct delta C-13-fingerprints, indicating a distinguishable contribution of C-4-biomass burning from peninsular India (PI). Tailored-model-predicted seasonaveraged BC concentrations (700 +/- 440 ng m(-3)) match observations (740 +/- 250 ng m(-3)), however, unveiling a systematically increasing model-observation bias (+19% to -53%) through winter. Inclusion of BC from open burning alone does not reconcile predictions (f(biomass) = 44 +/- 8%) with observations. Direct source-segregated comparison reveals regional offsets in anthropogenic emission fluxes in EIs, overestimated fossil-BC in the IGP, and underestimated biomass-BC in PI, which contributes to the model-observation bias. This ground-truthing pinpoints uncertainties in BC emission sources, which benefit both climate/air-quality modeling and mitigation policies in South Asia.
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| 8. |
- Grythe, Henrik, 1980-, et al.
(författare)
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A new aerosol wet removal scheme for the Lagrangian particle model FLEXPART
- 2017
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Ingår i: Geoscientific Model Development. - : Copernicus GmbH. - 1991-959X .- 1991-9603. ; 10:4, s. 1447-1466
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Tidskriftsartikel (refereegranskat)abstract
- A new and more physically based treatment of how removal by precipitation is calculated by FLEXPART is introduced, to take into account more aspects of aerosol diversity. Also new, is the definition of clouds and cloud properties. Results from simulations show good agreement with observed atmospheric concentrations for distinctly different aerosols. Atmospheric lifetimes were found to vary from a few hours (large aerosol particles) up to a month (small non-soluble).
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| 9. |
- Platt, Stephen M., et al.
(författare)
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Atmospheric composition in the European Arctic and 30 years of the Zeppelin Observatory, Ny-Ålesund
- 2022
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Ingår i: Atmospheric Chemistry And Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 22:5, s. 3321-3369
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Tidskriftsartikel (refereegranskat)abstract
- The Zeppelin Observatory (78.90∘ N, 11.88∘ E) is located on Zeppelin Mountain at 472 m a.s.l. on Spitsbergen, the largest island of the Svalbard archipelago. Established in 1989, the observatory is part of Ny-Ålesund Research Station and an important atmospheric measurement site, one of only a few in the high Arctic, and a part of several European and global monitoring programmes and research infrastructures, notably the European Monitoring and Evaluation Programme (EMEP); the Arctic Monitoring and Assessment Programme (AMAP); the Global Atmosphere Watch (GAW); the Aerosol, Clouds and Trace Gases Research Infrastructure (ACTRIS); the Advanced Global Atmospheric Gases Experiment (AGAGE) network; and the Integrated Carbon Observation System (ICOS). The observatory is jointly operated by the Norwegian Polar Institute (NPI), Stockholm University, and the Norwegian Institute for Air Research (NILU). Here we detail the establishment of the Zeppelin Observatory including historical measurements of atmospheric composition in the European Arctic leading to its construction. We present a history of the measurements at the observatory and review the current state of the European Arctic atmosphere, including results from trends in greenhouse gases, chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs), other traces gases, persistent organic pollutants (POPs) and heavy metals, aerosols and Arctic haze, and atmospheric transport phenomena, and provide an outline of future research directions.
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| 10. |
- Ruppel, Meri M., et al.
(författare)
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Observed and Modeled Black Carbon Deposition and Sources in the Western Russian Arctic 1800-2014
- 2021
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Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 55:8, s. 4368-4377
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Tidskriftsartikel (refereegranskat)abstract
- Black carbon (BC) particles contribute to climate warming by heating the atmosphere and reducing the albedo of snow/ice surfaces. The available Arctic BC deposition records are restricted to the Atlantic and North American sectors, for which previous studies suggest considerable spatial differences in trends. Here, we present first long-term BC deposition and radiocarbon-based source apportionment data from Russia using four lake sediment records from western Arctic Russia, a region influenced by BC emissions from oil and gas production. The records consistently indicate increasing BC fluxes between 1800 and 2014. The radiocarbon analyses suggest mainly (similar to 70%) biomass sources for BC with fossil fuel contributions peaking around 1960-1990. Backward calculations with the atmospheric transport model FLEXPART show emission source areas and indicate that modeled BC deposition between 1900 and 1999 is largely driven by emission trends. Comparison of observed and modeled data suggests the need to update anthropogenic BC emission inventories for Russia, as these seem to underestimate Russian BC emissions and since 1980s potentially inaccurately portray their trend. Additionally, the observations may indicate underestimation of wildfire emissions in inventories. Reliable information on BC deposition trends and sources is essential for design of efficient and effective policies to limit climate warming.
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