Abstract. In early October 2020, northern Europe experienced an episode with poor air quality due to high concentrations of particulate matter (PM). At several sites in Norway, recorded weekly values exceeded historical maximum PM10 concentrations from the past 4 to 10 years. Daily mean PM10 values at Norwegian sites were up to 97 µg m−3 and had a median value of 59 µg m−3. We analysed this severe pollution episode caused by long-range atmospheric transport based on surface and remote sensing observations and transport model simulations to understand its causes. Samples from three sites in mainland Norway and the Arctic remote station Zeppelin (Svalbard) showed strong contributions from mineral dust to PM10 (23 %–36 % as a minimum and 31 %–45 % as a maximum) and biomass burning (8 %–16 % to 19 %–21 %). Atmospheric transport simulations indicate that Central Asia was the main source region for mineral dust observed in this episode. The biomass burning fraction can be attributed to forest fires in Ukraine and southern Russia, but we cannot exclude other sources contributing, like fires elsewhere, because the model underestimates observed concentrations. The combined use of remote sensing, surface measurements, and transport modelling proved effective in describing the episode and distinguishing its causes.

Abstract. Volcanoes are a known source of halogens to the atmosphere. HBr volcanic emissions lead rapidly to the formation of BrO within volcanic plumes. BrO, having a longer residence time in the atmosphere than HBr, is expected to have an impact on tropospheric chemistry, at least at the local and regional scales. The objective of this paper is to prepare a framework for further 3-D modelling of volcanic halogen emissions in order to determine their fate within the volcanic plume and then in the atmosphere at the regional and global scales. This work is based on a 1-D configuration of the global chemistry transport model MOCAGE whose low computational cost allows us to perform a large set of sensitivity simulations. This paper studies the Mount Etna eruption on 10 May, 2008. Several reactions are added to MOCAGE to represent the halogen chemistry occurring within the volcanic plume. A simple sub-grid scale parameterization of the volcanic plume is also implemented and tested. The use of this parameterization tends to limit slightly the efficiency of BrO net production. Both simulations with and without the parameterization give similar results for the partitioning of the bromine species, ozone depletion and of the BrO / SO2 ratio that are consistent with previous studies and with the BrO / SO2 ratio in the volcanic plume estimated from GOME-2 spaceborne observations. A series of test experiments were performed to evaluate the sensitivity of the results to the composition of the emissions, and, in particular, primary sulphate aerosols, the Br radical, and NO. Simulations show that the plume chemistry is sensitive to these assumptions. Another series of tests on the effective radius assumed for the volcanic sulphate aerosols shows that BrO net production is sensitive to this parameter with lower BrO concentrations reached when larger aerosols (smaller total surface area) are assumed. We also find that the maximum altitude of the eruption changes the BrO production, which is linked to the vertical variability of the concentrations of oxidants. These sensitivity tests display changes in the bromine chemistry cycles that are generally at least as important as the subgrid scale plume parameterization. Overall, the version of the MOCAGE chemistry developed for this study is suitable to produce the expected halogen chemistry in volcanic plumes during daytime and night. These results will be used to guide the implementation of volcanic halogen emissions in the 3-D configuration of MOCAGE for regional and global simulations.

Mapping drought from space using, e.g., surface soil moisture (SSM), has become viable in the last decade. However, state of the art SSM retrieval products suffer from very poor coverage over northern latitudes. In this study, we propose an innovative drought indicator with a wider spatial and temporal coverage than that obtained from satellite SSM retrievals. We evaluate passive microwave brightness temperature observations from the Soil Moisture and Ocean Salinity (SMOS) satellite as a surrogate drought metric, and introduce a Standardized Brightness Temperature Index (STBI). The STBI is validated against drought indices from a land surface data assimilation system (LDAS-Monde), two satellite dervied SSM indices and a standardized precipitation index. Finally, we evaluate the STBI against the before mentioned drought indices in a case study of the 2018 Nordic drought. The STBI is found to be superior to the drought index created from satellite derived SSM in both spatial and temporal coverage over the Nordic region. Our results indicate that when compared to drought indices from precipitation data and a land data assimilation system, the STBI is able to capture the 2018 drought onset, severity and extent. Thus, the STBI index could provide additional information for drought monitoring in regions where the SSM retrieval problem is difficult.

Abstract. Volcanoes are known to be important emitters of atmospheric gases and aerosols, which for certain volcanoes can include halogen gases and in particular HBr. HBr emitted in this way can undergo rapid atmospheric oxidation chemistry (known as the bromine-explosion) within the volcanic emission plume leading to the production of bromine oxide (BrO) and ozone depletion. In this work, we present the results of a modelling study of a volcanic eruption from Mt Etna that occurred around Christmas 2018 that lasted 6 days. The aims of this study are to demonstrate and evaluate the ability of the regional 3D Chemistry Transport Model MOCAGE to simulate the volcanic halogen chemistry in this case study, to analyse the variability of the chemical processes during the plume transport, and to quantify its impact on the composition of the troposphere at a regional scale over the Mediterranean basin. The comparison of the tropospheric SO2 and BrO columns from 25 to 30 December 2018 from the MOCAGE simulation with the columns derived from the TROPOMI satellite measurements shows a very good agreement for the transport of the plumeand a good consistency for the concentrations if considering the uncertainties in the flux estimates and the TROPOMI columns. The analysis of the bromine species’ partitioning and of the associated chemical reaction rates provides a detailed picture of the simulated bromine chemistry throughout the diurnal cycle and at different stages of the volcanic plume’s evolution. The partitioning of the bromine species is modulated by the time evolution of the emissions during the 6 days of the eruption, by the meteorological conditions, and by the distance of the plume from the vent/the time since the emission. As the plume travels further from the vent, the halogen source gas HBr becomes depleted, BrO production in the plume becomes less efficient, and ozone depletion (proceeding via the Br + O3 reaction followed by the BrO self-reaction) decreases. The depletion of HBr relative to the other prevalent hydracid HCl leads to a shift in the relative concentrations of the Br− and Cl− ions, which in turn leads to reduced production of Br2 relative to BrCl. The MOCAGE simulations show a regional impact of the volcanic eruption on the oxidants OH and O3 with a reduced burden of both gases that is caused by the chemistry in the volcanic plume. This reduction in atmospheric oxidation capacity results in a reduced CH4 burden. Finally, sensitivity tests on the composition of the emissions carried out in this work show that the production of BrO is higher when the volcanic emissions of sulfate aerosols are increased but occurs very slowly when no sulfate and Br radicals are assumed to be in the emissions. Both sensitivity tests highlight a significant impact on the oxidants in the troposphere at the regional scale of these assumptions. All the results of this modelling study are consistent with the previous studies carried out on the volcanic halogens modelling.

Abstract. HBr emissions from volcanoes lead rapidly to the formation of BrO within volcanic plumes and have an impact on tropospheric chemistry, at least at the local and regional scales. The motivation of this paper is to prepare a framework for further 3D modelling of volcanic halogen emissions in order to determine their fate within the volcanic plume and then in the atmosphere at the regional and global scales. The main aim is to evaluate the ability of the model to produce a realistic partitioning of bromine species within a grid box size typical of MOCAGE (Model Of atmospheric Chemistry At larGE scale) 3D (0.5∘ × 0.5∘). This work is based on a 1D single-column configuration of the global chemistry-transport model MOCAGE that has low enough computational cost to allow us to perform a large set of sensitivity simulations. This paper uses the emissions from the Mount Etna eruption on 10 May 2008. Several reactions are added to MOCAGE to represent the volcanic plume halogen chemistry. A simple plume parameterisation is also implemented and tested. The use of this parameterisation tends to only slightly limit the efficiency of BrO net production. Both simulations with and without the parameterisation give results for the partitioning of the bromine species, of ozone depletion and of the BrO/SO2 ratio that are consistent with previous studies. A series of test experiments were performed to evaluate the sensitivity of the results to the composition of the emissions (primary sulfate aerosols, Br radical and NO) and to the effective radius assumed for the volcanic sulfate aerosols. Simulations show that the plume chemistry is sensitive to all these parameters. We also find that the maximum altitude of the eruption changes the BrO production, which is linked to the vertical variability of the concentrations of oxidants in the background air. These sensitivity tests display changes in the bromine chemistry cycles that are generally at least as important as the plume parameterisation. Overall, the version of the MOCAGE chemistry developed for this study is suitable to produce the expected halogen chemistry in volcanic plumes during daytime and night-time.