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  • 11
    In: Geoscientific Model Development, Copernicus GmbH, Vol. 13, No. 11 ( 2020-11-20), p. 5707-5723
    Abstract: Abstract. Excessive numerical diffusion is one of the major limitations in the representation of long-range transport by chemistry transport models. In the present study, we focus on excessive diffusion in the vertical direction, which has been shown to be a major issue, and we explore three possible ways of addressing this problem: increasing the vertical resolution, using an advection scheme with anti-diffusive properties and more accurately representing the vertical wind. This study was carried out using the CHIMERE chemistry transport model for the 18 March 2012 eruption of Mount Etna, which released about 3 kt of sulfur dioxide into the atmosphere in a plume that was observed by satellite instruments (the Infrared Atmospheric Sounding Interferometer instrument, IASI, and the Ozone Monitoring Instrument, OMI) for several days. The change from the classical Van Leer (1977) scheme to the Després and Lagoutière (1999) anti-diffusive scheme in the vertical direction was shown to provide the largest improvement to model outputs in terms of preserving the thin plume emitted by the volcano. To a lesser extent, the improved representation of the vertical wind field was also shown to reduce plume dispersion. Both of these changes helped to reduce vertical diffusion in the model as much as a brute-force approach (increasing vertical resolution).
    Type of Medium: Online Resource
    ISSN: 1991-9603
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2020
    detail.hit.zdb_id: 2456725-5
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  • 12
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 121, No. 12 ( 2016-06-27), p. 7461-7488
    Abstract: Observations from the CONTRAST campaign in the tropical western Pacific are used to infer the concentration of tropospheric OH The empirically based value of tropospheric column OH is 0 to 20% larger than found within global models Underestimations of observed NO x , CH 3 CHO, and HCHO drive most differences between column OH within global models and empirically based value
    Type of Medium: Online Resource
    ISSN: 2169-897X , 2169-8996
    URL: Issue
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2016
    detail.hit.zdb_id: 710256-2
    detail.hit.zdb_id: 2016800-7
    SSG: 16,13
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  • 13
    Online Resource
    Online Resource
    Informa UK Limited ; 2007
    In:  Journal of the Air & Waste Management Association Vol. 57, No. 11 ( 2007-11), p. 1360-1369
    In: Journal of the Air & Waste Management Association, Informa UK Limited, Vol. 57, No. 11 ( 2007-11), p. 1360-1369
    Type of Medium: Online Resource
    ISSN: 1096-2247 , 2162-2906
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2007
    detail.hit.zdb_id: 1003064-5
    detail.hit.zdb_id: 2048696-0
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  • 14
    In: Comptes Rendus. Géoscience, Cellule MathDoc/Centre Mersenne, Vol. 347, No. 3 ( 2015-05-01), p. 134-144
    Type of Medium: Online Resource
    ISSN: 1778-7025
    Language: English
    Publisher: Cellule MathDoc/Centre Mersenne
    Publication Date: 2015
    detail.hit.zdb_id: 2079109-4
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  • 15
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 111, No. D23 ( 2006-12-16)
    Abstract: Aircraft measurements of water‐soluble organic carbon (WSOC) aerosol over NE North America during summer 2004 (ITCT‐2K4) are simulated with a global chemical transport model (GEOS‐Chem) to test our understanding of the sources of organic carbon (OC) aerosol in the free troposphere (FT). Elevated concentrations were observed in plumes from boreal fires in Alaska and Canada. WSOC aerosol concentrations outside of these plumes average 0.9 ± 0.9 μ g C m −3 in the FT (2–6 km). The corresponding model value is 0.7 ± 0.6 μ g C m −3 , including 42% from biomass burning, 36% from biogenic secondary organic aerosol (SOA), and 22% from anthropogenic emissions. Previous OC aerosol observations over the NW Pacific in spring 2001 (ACE‐Asia) averaged 3.3 ± 2.8 μ g C m −3 in the FT, compared to a model value of 0.3 ± 0.3 μ g C m −3 . WSOC aerosol concentrations in the boundary layer (BL) during ITCT‐2K4 are consistent with OC aerosol observed at the IMPROVE surface network. The model is low in the boundary layer by 30%, which we attribute to secondary formation at a rate comparable to primary anthropogenic emission. Observed WSOC aerosol concentrations decrease by a factor of 2 from the BL to the FT, as compared to a factor of 10 decrease for sulfate, indicating that most of the WSOC aerosol in the FT originates in situ. Despite reproducing mean observed WSOC concentrations in the FT to within 25%, the model cannot account for the variance in the observations ( R = 0.21). Covariance analysis of FT WSOC aerosol with other measured chemical variables suggests an aqueous‐phase mechanism for SOA generation involving biogenic precursors.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2006
    detail.hit.zdb_id: 161666-3
    SSG: 16,13
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  • 16
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 18, No. 1 ( 2018-01-16), p. 445-465
    Abstract: Abstract. Carbon monoxide, CO, and fine atmospheric particulate matter, PM2.5, are analyzed over the Guinean Gulf coastal region using the WRF-CHIMERE modeling system and observations during the beginning of the monsoon 2006 (from May to July), corresponding to the Africa Multidisciplinary Monsoon Analysis (AMMA) campaign period. Along the Guinean Gulf coast, the contribution of long-range pollution transport to CO or PM2.5 concentrations is important. The contribution of desert dust PM2.5 concentration decreases from ∼ 38 % in May to ∼ 5 % in July. The contribution of biomass burning PM2.5 concentration from Central Africa increases from ∼ 10 % in May to ∼ 52 % in July. The anthropogenic contribution is ∼ 30 % for CO and ∼ 10 % for PM2.5 during the whole period. When focusing only on anthropogenic pollution, frequent northward transport events from the coast to the Sahel are associated with periods of low wind and no precipitation. In June, anthropogenic PM2.5 and CO concentrations are higher than in May or July over the Guinean coastal region. Air mass dynamics concentrate pollutants emitted in the Sahel due to a meridional atmospheric cell. Moreover, a part of the pollution emitted remotely at the coast is transported and accumulated over the Sahel. Focusing the analysis on the period 8–15 June, anthropogenic pollutants emitted along the coastline are exported toward the north especially at the beginning of the night (18:00 to 00:00 UTC) with the establishment of the nocturnal low level jet. Plumes originating from different cities are mixed for some hours at the coast, leading to high pollution concentration, because of specific disturbed meteorological conditions.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2069847-1
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  • 17
    In: Geoscientific Model Development, Copernicus GmbH, Vol. 10, No. 6 ( 2017-06-28), p. 2397-2423
    Abstract: Abstract. CHIMERE is a chemistry-transport model designed for regional atmospheric composition. It can be used at a variety of scales from local to continental domains. However, due to the model design and its historical use as a regional model, major limitations had remained, hampering its use at hemispheric scale, due to the coordinate system used for transport as well as to missing processes that are important in regions outside Europe. Most of these limitations have been removed in the CHIMERE-2017 version, allowing its use in any region of the world and at any scale, from the scale of a single urban area up to hemispheric scale, with or without polar regions included. Other important improvements have been made in the treatment of the physical processes affecting aerosols and the emissions of mineral dust. From a computational point of view, the parallelization strategy of the model has also been updated in order to improve model numerical performance and reduce the code complexity. The present article describes all these changes. Statistical scores for a model simulation over continental Europe are presented, and a simulation of the circumpolar transport of volcanic ash plume from the Puyehue volcanic eruption in June 2011 in Chile provides a test case for the new model version at hemispheric scale.
    Type of Medium: Online Resource
    ISSN: 1991-9603
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2017
    detail.hit.zdb_id: 2456725-5
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  • 18
    In: Geoscientific Model Development, Copernicus GmbH, Vol. 10, No. 2 ( 2017-02-23), p. 927-944
    Abstract: Abstract. The presence of airborne aerosols affects the meteorology as it induces a perturbation in the radiation budget, the number of cloud condensation nuclei and the cloud micro-physics. Those effects are difficult to model at regional scale as regional chemistry-transport models are usually driven by a distinct meteorological model or data. In this paper, the coupling of the CHIMERE chemistry-transport model with the WRF meteorological model using the OASIS3-MCT coupler is presented. WRF meteorological fields along with CHIMERE aerosol optical properties are exchanged through the coupler at a high frequency in order to model the aerosol–radiation interactions. The WRF-CHIMERE online model has a higher computational burden than both models run separately in offline mode (up to 42 % higher). This is mainly due to some additional computations made within the models such as more frequent calls to meteorology treatment routines or calls to optical properties computation routines. On the other hand, the overall time required to perform the OASIS3-MCT exchanges is not significant compared to the total duration of the simulations. The impact of the coupling is evaluated on a case study over Europe, northern Africa, the Middle East and western Asia during the summer of 2012, through comparisons of the offline and two online simulations (with and without the aerosol optical properties feedback) to observations of temperature, aerosol optical depth (AOD) and surface PM10 (particulate matter with diameters lower than 10 µm) concentrations. The result shows that using the optical properties feedback induces a radiative forcing (average forcing of −4.8 W m−2) which creates a perturbation in the average surface temperatures over desert areas (up to 2.6° locally) along with an increase in both AOD and PM10 concentrations.
    Type of Medium: Online Resource
    ISSN: 1991-9603
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2017
    detail.hit.zdb_id: 2456725-5
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  • 19
    In: Remote Sensing, MDPI AG, Vol. 14, No. 11 ( 2022-05-31), p. 2625-
    Abstract: A bulk of evidence from in situ observations and lab experiments suggests that brown carbon (light-absorbing organic compounds in particles) can provide a significant yet highly variable contribution to the overall light absorption by aerosol particles from biomass burning (BB). Partly stemming from the complexity of the atmospheric evolution of organic aerosol (OA), the variability in brown carbon (BrC) absorption makes it difficult to partition the radiative effects of BrC and black carbon (BC) in atmospheric and climate models; as such, there are calls for satellite-based methods that could provide a statistical characterization of BrC absorption and its evolution in different regions of the world, especially in remote BB regions, such as Siberia. This study examined the feasibility of the statistical characterization of the evolution of BrC absorption and related parameters of BB aerosol in smoke plumes from intense wildfires in Siberia through the analysis of a combination of data from three satellite instruments: OMI (Ozone Monitoring Instrument), MISR (Multi-Angle Imaging SpectroRadiometer), and MODIS (Moderate Resolution Imaging Spectroradiometer). Using a Monte Carlo method, which related the satellite retrievals of the absorption and extinction aerosol optical depths to Mie theory calculations of the optical properties of BB aerosol, we found that the BrC absorption, as well as the imaginary refractive index for the OA, decreased significantly in Siberian BB smoke plumes during about 30 h of the daylight evolution, nevertheless remaining considerable until at least 70 h of the daylight evolution. Overall, the study indicated that the analysis of multi-platform satellite observations of BB plumes can provide useful insights into the atmospheric evolution of BrC absorption and the partitioning of BrC and BC contributions to the total light absorption by BB aerosol.
    Type of Medium: Online Resource
    ISSN: 2072-4292
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
    detail.hit.zdb_id: 2513863-7
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  • 20
    In: Remote Sensing, MDPI AG, Vol. 14, No. 11 ( 2022-05-27), p. 2582-
    Abstract: We present a novel passive satellite remote sensing approach for observing the three-dimensional distribution of aerosols emitted from wildfires. This method, called AEROS5P, retrieves vertical profiles of aerosol extinction from cloud-free measurements of the TROPOMI satellite sensor onboard the Sentinel 5 Precursor mission. It uses a Tikhonov–Phillips regularization, which iteratively fits near-infrared and visible selected reflectances to simultaneously adjust the vertical distribution and abundance of aerosols. The information on the altitude of the aerosol layers is provided by TROPOMI measurements of the reflectance spectra at the oxygen A-band near 760 nm. In the present paper, we use this new approach for observing the daily evolution of the three-dimensional distribution of biomass burning aerosols emitted by Australian wildfires on 20–24 December 2019. Aerosol optical depths (AOD) derived by vertical integration of the aerosol extinction profiles retrieved by AEROS5P are compared with MODIS, VIIRS and AERONET coincident observations. They show a good agreement in the horizontal distribution of biomass burning aerosols, with a correlation coefficient of 0.87 and a mean absolute error of 0.2 with respect to VIIRS. Moderately lower correlations (0.63) were found between AODs from AEROS5P and MODIS, while the range of values for this comparison was less than half of that with respect to VIIRS. A fair agreement was found between coincident transects of vertical profiles of biomass burning aerosols derived from AEROS5P and from the CALIOP spaceborne lidar. The mean altitudes of these aerosols derived from these two measurements showed a good agreement, with a small mean bias (185 m) and a correlation coefficient of 0.83. Moreover, AEROS5P observations reveal the height of injection of the biomass burning aerosols in 3D. The highest injection heights during the period of analysis were coincident with the largest fire radiative power derived from MODIS. Consistency was also found with respect to the vertical stability of the atmosphere. The AEROS5P approach provides retrievals for cloud-free scenes over several regions, although currently limited to situations with a dominating presence of smoke particles. Future developments will also aim at observing other aerosol species.
    Type of Medium: Online Resource
    ISSN: 2072-4292
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
    detail.hit.zdb_id: 2513863-7
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