63 research outputs found

    The ash dispersion over Europe during the Eyjafjallajökull eruption e Comparison of CMAQ simulations to remote sensing and air-borne in-situ observations

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    The dispersion of volcanic ash over Europe after the outbreak of the Eyjafjallajökull on Iceland on 14 April 2010 has been simulated with a conventional three-dimensional Eulerian chemistry transport model system, the Community Multiscale Air Quality (CMAQ) model. Four different emission scenarios representing the lower and upper bounds of the emission height and intensity were considered. The atmospheric ash concentrations turned out to be highly variable in time and space. The model results were compared to three different kinds of observations: Aeronet aerosol optical depth (AOD) measurements, Earlinet aerosol extinction profiles and in-situ observations of the ash concentration by means of optical particle counters aboard the DLR Falcon aircraft. The model was able to reproduce observed AOD values and atmospheric ash concentrations. Best agreement was achieved for lower emission heights and a fraction of 2% transportable ash in the total volcanic emissions. The complex vertical structure of the volcanic ash layers in the free troposphere could not be simulated. Compared to the observations, the model tends to show vertically more extended, homogeneous aerosol layers. This is caused by a poor vertical resolution of the model at higher altitudes and a lack of information about the vertical distribution of the volcanic emissions. Only a combination of quickly available observations of the volcanic ash cloud and atmospheric transport models can give a comprehensive picture of ash concentrations in the atmosphere

    Detrainment Dominates CCN Concentrations Around Non Precipitating Convective Clouds Over the Amazon

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    We investigated the relationship between the number concentration of cloud droplets (Nd) in ice-free convective clouds and of particles large enough to act as cloud condensation nuclei (CCN) measured at the lateral boundaries of cloud elements. The data were collected during the ACRIDICON CHUVA aircraft campaign over the Amazon Basin. The results indicate that the CCN particles at the lateral cloud boundaries are dominated by detrainment from the cloud

    Illustration of microphysical processes in Amazonian deep convective clouds in the gamma phase space: introduction and potential applications

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    The behavior of tropical clouds remains a major open scientific question, resulting in poor representation by models. One challenge is to realistically reproduce cloud droplet size distributions (DSDs) and their evolution over time and space. Many applications, not limited to models, use the gamma function to represent DSDs. However, even though the statistical characteristics of the gamma parameters have been widely studied, there is almost no study dedicated to understanding the phase space of this function and the associated physics. This phase space can be defined by the three parameters that define the DSD intercept, shape, and curvature. Gamma phase space may provide a common framework for parameterizations and intercomparisons. Here, we introduce the phase space approach and its characteristics, focusing on warm-phase microphysical cloud properties and the transition to the mixed-phase layer. We show that trajectories in this phase space can represent DSD evolution and can be related to growth processes. Condensational and collisional growth may be interpreted as pseudo-forces that induce displacements in opposite directions within the phase space. The actually observed movements in the phase space are a result of the combination of such pseudo-forces. Additionally, aerosol effects can be evaluated given their significant impact on DSDs. The DSDs associated with liquid droplets that favor cloud glaciation can be delimited in the phase space, which can help models to adequately predict the transition to the mixed phase. We also consider possible ways to constrain the DSD in two-moment bulk microphysics schemes, in which the relative dispersion parameter of the DSD can play a significant role. Overall, the gamma phase space approach can be an invaluable tool for studying cloud microphysical evolution and can be readily applied in many scenarios that rely on gamma DSDs

    Aerosol characteristics and particle production in the upper troposphere over the Amazon Basin

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    Airborne observations over the Amazon Basin showed high aerosol particle concentrations in the upper troposphere (UT) between 8 and 15 km altitude, with number densities (normalized to standard temperature and pressure) often exceeding those in the planetary boundary layer (PBL) by 1 or 2 orders of magnitude. The measurements were made during the German–Brazilian cooperative aircraft campaign ACRIDICON–CHUVA, where ACRIDICON stands for Aerosol, Cloud, Precipitation, and Radiation Interactions and Dynamics of Convective Cloud Systems and CHUVA is the acronym for Cloud Processes of the Main Precipitation Systems in Brazil: A Contribution to Cloud Resolving Modeling and to the GPM (global precipitation measurement), on the German High Altitude and Long Range Research Aircraft (HALO). The campaign took place in September–October 2014, with the objective of studying tropical deep convective clouds over the Amazon rainforest and their interactions with atmospheric trace gases, aerosol particles, and atmospheric radiation. Aerosol enhancements were observed consistently on all flights during which the UT was probed, using several aerosol metrics, including condensation nuclei (CN) and cloud condensation nuclei (CCN) number concentrations and chemical species mass concentrations. The UT particles differed sharply in their chemical composition and size distribution from those in the PBL, ruling out convective transport of combustion-derived particles from the boundary layer (BL) as a source. The air in the immediate outflow of deep convective clouds was depleted of aerosol particles, whereas strongly enhanced number concentrations of small particles ( 90 nm) particles in the UT, which consisted mostly of organic matter and nitrate and were very effective CCN. Our findings suggest a conceptual model, where production of new aerosol particles takes place in the continental UT from biogenic volatile organic material brought up by deep convection and converted to condensable species in the UT. Subsequently, downward mixing and transport of upper tropospheric aerosol can be a source of particles to the PBL, where they increase in size by the condensation of biogenic volatile organic compound (BVOC) oxidation products. This may be an important source of aerosol particles for the Amazonian PBL, where aerosol nucleation and new particle formation have not been observed. We propose that this may have been the dominant process supplying secondary aerosol particles in the pristine atmosphere, making clouds the dominant control of both removal and production of atmospheric particles

    Arthur Schnitzler : Lieben, Träumen, Sterben.

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    The volcanic ash plume near the Eyjafjallajökull on 1-2 May 2010

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    This paper describes the analysis of airborne measurements and model simulations of the volcanic ash plume close to Iceland’s Eyjafjallajökull volcano in April/May 2010. In particular we quantify the plume properties for the period of 1 to 2 May, 2010, up to 450 km downstream the volcano. The measurements provide information on the plume width, upper height, mean depth, wind speed profile, attenuated Lidar backscatter profile, plume temperature, ash particle sizes, ash mass concentration, ash particle size distribution, humidity, O3, CO and SO2 mixing ratio, ash optical depth, volume flux, and mass flux. Here we report about analysis of the optical depth from the Lidar observations using the shadow method, and on comparisons of modeled and measured plume properties constraining the ash properties

    Simulations of the 2010 Eyjafjallajökull volcanic ash dispersal over Europe using COSMO-MUSCAT

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    The ash plume of the Icelandic volcano Eyjafjallajökull covering Europe in April and May 2010 has notably attracted the interest of atmospheric researchers. Emission, transport, and deposition of the volcanic ash are simulated with the regional chemistry-transport model COSMOeMUSCAT. Key input parameters for transport models are the ash injection height, which controls the ash layer height during long-range transport, and the initial particle size distribution, which influences the sedimentation velocity. For each model layer, relative release rates are parameterised using stereo-derived plume heights from NASA’s space-borne Multi-angle Imaging SpectroRadiometer (MISR) observations near the source. With this model setup the ash is emitted at several levels beneath the maximum plume heights reported by the Volcanic Ash Advisory Centre (VAAC) London. The initial particle size distribution used in COSMOeMUSCAT is derived from airborne in-situ measurements. In addition, the impact of different injection heights on the vertical distribution of the volcanic ash plume over Europe is shown. Ash emissions at specific control levels allow to assess the relative contribution of each layer to the spatial distribution after transport. The model results are compared to aerosol optical depths from European Sun photometer sites, lidar profiles measured over Leipzig/Germany, and ground-based microphysical measurements from several German air quality stations. In particular the good agreement between modelled vertical profiles of volcanic ash and lidar observations indicates that using the MISR stereoheight retrievals to characterize atmospheric ash input provide an alternative to injection height models in case of lacking information on eruption dynamics

    On the visibility of airborne volcanic ash and mineral dust from the pilot’s perspective in flight

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    In April 2010, volcanic ash from the Eyjafjalla volcano in Iceland strongly impacted aviation in Europe. In order to prevent a similar scenario in the future, a threshold value for safe aviation based on actual mass concentrations was introduced (2 mg m3 in Germany). This study contrasts microphysical and optical properties of volcanic ash and mineral dust and assesses the detectability of potentially dangerous ash layers (mass concentration larger than 2 mg m3) from a pilot’s perspective during a flight. Also the possibility to distinguish between volcanic ash and other aerosols is investigated. The visual detectability of airborne volcanic ash is addressed based on idealized radiative transfer simulations and on airborne observations with the DLR Falcon gathered during the Eyjafjalla volcanic ash research flights in 2010 and during the Saharan Mineral Dust Experiments in 2006 and 2008. Mineral dust and volcanic ash aerosol both show an enhanced coarse mode (>1 lm) aerosol concentration, but volcanic ash aerosol additionally contains a significant number of Aitken mode particles (<150 nm) not present in mineral dust. Under daylight clear-sky conditions and depending on the viewing geometry, volcanic ash is visible already at mass concentrations far below what is currently considered dangerous for aircraft engines. However, it is not possible to visually distinguish volcanic ash from other aerosol layers or to determine whether a volcanic ash layer is potentially dangerous (mass concentration larger or smaller than 2mgm3). Different appearances due to microphysical differences of both aerosol types are not detectable by the human eye. Nonetheless, as ash concentrations can vary significantly over distances travelled by an airplane within seconds, this visual threat evaluation may contribute greatly to the short-term response of pilots in ash-contaminated air space

    A case study of observations of volcanic ash from the Eyjafjallajökull eruption: 1. In situ airborne observations

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    On 17 May 2010, the FAAM BAe-146 aircraft made remote and in situ measurements of the volcanic ash cloud from Eyjafjallaj�¶kull over the southern North Sea. The Falcon 20E aircraft operated by Deutsches Zentrum f�¼r Luft- und Raumfahrt (DLR) also sampled the ash cloud on the same day. While no â��wingtip-to-wingtipâ�� co-ordination was performed, the proximity of the two aircraft allows worthwhile comparisons. Despite the high degree of inhomogeneity (e.g., column ash loadings varied by a factor of three over �100 km) the range of ash mass concentrations and the ratios between volcanic ash mass and concentrations of SO2, O3 and CO were consistent between the two aircraft and within expected instrumental uncertainties. The data show strong correlations between ash mass, SO2 concentration and aerosol scattering with the FAAM BAe-146 data providing a specific extinction coefficient of 0.6â��0.8 m2 g�1. There were significant differences in the observed ash size distribution with FAAM BAe-146 data showing a peak in the mass at �3.5 mm (volume-equivalent diameter) and DLR data peaking at �10 mm. Differences could not be accounted for by refractive index and shape assumptions alone. The aircraft in situ and lidar data suggest peak ash concentrations of 500â��800 mg m�3 with a factor of two uncertainty. Comparing the location of ash observations with the ash dispersion model output highlights differences that demonstrate the difficulties in forecasting such events and the essential nature of validating models using high quality observational data from platforms such as the FAAM BAe-146 and the DLR Falcon
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