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We present MISTRA-v9.0, a one-dimensional (1D) and box (0D) atmospheric chemistry model. The model includes a detailed particle description with regards to the microphysics, gas–particle interactions, and liquid-phase chemistry within particles. Version 9.0 (v9.0) is the first release of MISTRA as an open-source community model. A major review of the code has been performed along with this public version release to improve the user friendliness and platform independence of the model. The purpose of this public release is to maximise the benefit of MISTRA to the community by making the model freely available and easier to use and develop. This paper presents a thorough description of the model characteristics and components. We show some examples of simulations reproducing previous studies with MISTRA, finding that v9.0 is consistent with previous versions. [ABSTRACT FROM AUTHOR]

An intercomparison between 10 single-column (SCM) and 5 large-eddy simulation (LES) models is presented for a radiation fog case study inspired by the Local and Non-local Fog Experiment (LANFEX) field campaign. Seven of the SCMs represent single-column equivalents of operational numerical weather prediction (NWP) models, whilst three are research-grade SCMs designed for fog simulation, and the LESs are designed to reproduce in the best manner currently possible the underlying physical processes governing fog formation. The LES model results are of variable quality and do not provide a consistent baseline against which to compare the NWP models, particularly under high aerosol or cloud droplet number concentration (CDNC) conditions. The main SCM bias appears to be toward the overdevelopment of fog, i.e. fog which is too thick, although the inter-model variability is large. In reality there is a subtle balance between water lost to the surface and water condensed into fog, and the ability of a model to accurately simulate this process strongly determines the quality of its forecast. Some NWP SCMs do not represent fundamental components of this process (e.g. cloud droplet sedimentation) and therefore are naturally hampered in their ability to deliver accurate simulations. Finally, we show that modelled fog development is as sensitive to the shape of the cloud droplet size distribution, a rarely studied or modified part of the microphysical parameterisation, as it is to the underlying aerosol or CDNC. [ABSTRACT FROM AUTHOR]

An intercomparison between 10 single-column (SCM) and 5 large-eddy simulation (LES) models is presented for a radiation fog case study inspired by the LANFEX field campaign. 7 of the SCMs represent single-column equivalents of operational numerical weather prediction (NWP) models, whilst 3 are research-grade SCMs designed for fog simulation, and the LES are designed to reproduce in the best manner currently possible the underlying physical processes governing fog formation. The LES model results are of variable quality, and do not provide a consistent baseline against which to compare the NWP models, particularly under high aerosol or cloud droplet number (CDNC) conditions. The main SCM bias appears to be toward over-development of fog, i.e. fog which is too thick, although the inter-model variability is large. In reality there is a subtle balance between water lost to the surface and water condensed into fog, and the ability of a model to accurately simulate this process strongly determines the quality of its forecast. Some NWP-SCMs do not represent fundamental components of this process (e.g. cloud droplet sedimentation) and therefore are naturally hampered in their ability to deliver accurate simulations. Finally, we show that modelled fog development is as sensitive to the shape of the cloud droplet size distribution, a rarely studied or modified part of the microphysical parametrization, as it is to the underlying aerosol or CDNC. [ABSTRACT FROM AUTHOR]

We present MISTRA-v9.0, a one dimensional (1D) atmospheric chemistry model. The model includes a detailed particle description with regards to the microphysics, gas-particle interactions, and liquid phase chemistry within particles. Version 9.0 is the first release of MISTRA as an open-source community model. A major review of the code has been performed along with this public version release to improve the user-friendliness and platform-independence of the model. In the past 20 years, MISTRA has been used in over 25 studies to address a wide range of scientific questions. The purpose of this public release is to maximise the benefit of MISTRA to the community by making the model freely available and easier to use and develop. This paper presents a thorough description of the model characteristics and components. We show some examples of simulations reproducing previous studies with MISTRA, finding that version 9.0 is consistent with previous versions. [ABSTRACT FROM AUTHOR]

The impact of six heterogeneous gas--aerosol up-take reactions on tropospheric ozone and nitrogen species was studied using two chemical transport models, the Meteorological Synthesizing Centre-West of the European Monitoring and Evaluation Programme (EMEP MSC-W) and the European Centre Hamburg general circulation model combined with versions of the Hamburg Aerosol Model and Model for Ozone and Related chemical Tracers (ECHAMHAMMOZ). Species undergoing heterogeneous reactions in both models include N2O5, NO3, NO2, O3, HNO3, and HO2. Since heterogeneous reactions take place at the aerosol surface area, the modelled surface area density (Sa) of both models was compared to a satellite product retrieving the surface area. This comparison shows a good agreement in global pattern and especially the capability of both models to capture the extreme aerosol loadings in east Asia. The impact of the heterogeneous reactions was evaluated by the simulation of a reference run containing all heterogeneous reactions and several sensitivity runs. One reaction was turned off in each sensitivity run to compare it with the reference run. The analysis of the sensitivity runs confirms that the globally most important heterogeneous reaction is the one of N2O5. Nevertheless, NO2, HNO3, and HO2 heterogeneous reactions gain relevance particularly in east Asia due to the presence of high NOx concentrations and high Sa in the same region. The heterogeneous reaction of O3 itself on dust is of minor relevance compared to the other heterogeneous reactions. The impacts of the N2O5 reactions show strong seasonal variations, with the biggest impacts on O3 in springtime when photochemical reactions are active and N2O5 levels still high. Evaluation of the models with northern hemispheric ozone surface observations yields a better agreement of the models with observations in terms of concentration levels, variability, and temporal correlations at most sites when the heterogeneous reactions are incorporated. Our results are loosely consistent with results from earlier studies, although the magnitude of changes induced by N2O5 reaction is at the low end of estimates, which seems to fit a trend, whereby the more recent the study the lower the impacts of these reactions. [ABSTRACT FROM AUTHOR]

The impact of six heterogeneous gas-aerosol uptake reactions on tropospheric ozone and nitrogen species was studied using two chemical transport models, EMEP MSC-W and ECHAM-HAMMOZ. Species undergoing heterogeneous reactions in both models include N2O5, NO3, NO2, O3, HNO3 and HO2. Since heterogeneous reactions take place at the aerosol surface area, the modeled surface area density Sa of both models was compared to a satellite product retrieving the surface area. This comparison shows a good agreement in global pattern and especially the capability of both models to capture the extreme aerosol loadings in East Asia. The impact of the heterogeneous reactions was evaluated by the simulation of a reference run containing all heterogeneous reactions and several sensitivity runs. One reaction was turned off in each sensitivity run to compare it with the reference run. The analysis of the sensitivity runs confirms that the globally most important heterogeneous reaction is the one of N2O5. Nevertheless, NO2, HNO3 and HO2 heterogeneous reaction gain relevance particularly in East Asia due to the presence of high NOx concentrations and high Sa in the same region, although ECHAM-HAMMOZ showed much stronger responses than EMEP in this respect. The heterogeneous reaction of O3 itself on dust is of minor relevance compared to the other heterogeneous reactions. The impacts of the N2O5 reactions show strong seasonal variations, with biggest impacts on O3 in spring time when photochemical reactions are active and N2O5 levels still high. Evaluation of the models with northern hemispheric ozone surface observations yields a better agreement of the models with observations in terms of concentration levels, variability, and temporal correlations at most sites when the heterogeneous reactions are incorporated. [ABSTRACT FROM AUTHOR]