Joakim Langner

An Eulerian Limited-Area Atmospheric Transport Model

Abstract A limited-area, offline, Eulerian atmospheric transport model has been developed. The model is based on a terrain-following vertical coordinate and a mass-conserving, positive definite advection scheme with small phase and amplitude errors. The objective has been to develop a flexible, all-purpose offline model. The model includes modules for emission input, vertical turbulent diffusion, and deposition processes. The model can handle an arbitrary number of chemical components and provides a framework for inclusion of modules describing physical and chemical transformation processes between different components. Idealized test cases, as well as simulations of the atmospheric distribution of 222Rn, demonstrate the ability of the model to meet the requirements of mass conservation and positiveness and to produce realistic simulations of a simple atmospheric tracer.

Interannual variation and trends in air pollution over Europe due to climate variability during 1958–2001 simulated with a regional CTM coupled to the ERA40 reanalysis

Measurements of changes in the atmospheric O2/N2 ratio have typically relied on compressed air derived from highpressure tanks as the reference material against which atmospheric changes are assessed. The validity of this procedure is examined here in the context of the history of 18 O2/N2 reference tanks compared over a 12-yr time-frame. By considering differences in tank sizes, material types, and by performing additional tests, the long-term stability of the delivered gas is evaluated with respect to surface reactions, leakage, regulator effects, and thermal diffusion and gravimetric fractionation. Results are also reported for the stability of CO2 in these tanks. The results emphasize the importance of orienting tanks horizontally within a thermally insulated enclosure to reduce thermal and gravimetric fractionation of both O2/N2 and CO2 concentrations, and they emphasize the importance of avoiding elastomeric Orings at the head-valve base. With the procedures documented here, the long-term drift in O2/N2 appears to be zero to within approximately ±0.4 per meg yr-1, which projects to an uncertainty of ±0.16 Pg C yr-1 (1ó) in O2-based global carbon budgets.

Comparison of five eulerian air pollution forecasting systems for the summer of 1999 using the German ozone monitoring data

Eulerian state-of-the-art air pollution forecasting systems on the European scale are operated routinely by several countries in Europe. DWD and FUB, both Germany, NERI, Denmark, NILU, Norway, and SMHI, Sweden, operate some of these systems. To apply such modeling systems, e.g. for regulatory purposes according to new EU directives, an evaluation and comparison of the model systems is fundamental in order to assess their reliability. One step in this direction is presented in this study: The model forecasts from all five systems have been compared to measurements of ground level ozone in Germany. The outstanding point in this investigation is the availability of a huge amount of data – from forecasts by the different model systems and from observations. This allows for a thorough interpretation of the findings and assures the significance of the observed features. Data from more than 300 measurement stations for a 5-month period (May–September 1999) of the German monitoring networks have been used in this comparison. Different spatial and temporal statistical parameters were applied in the evaluation. Generally, it was found that the most comprehensive models gave the best results. However, the less comprehensive and computational cheaper models also produced good results. The extensive comparison made it possible to point out weak points in the different models and to describe the individual model behavior for a full summer period in a climatological sense. The comparison also gave valuable information for an assessment of individual measurement stations and complete monitoring networks in terms of the representativeness of the observation data.

Global scale transport of acidifying pollutants

During the past few years several attempts have been made to use three-dimensional tracer transport models to simulate the global distribution of sulfur and nitrogen compounds from both natural and anthropogenic sources. We review these studies and show examples of estimated distributions of the total deposition of sulfur, oxidized nitrogen and ammonium as well as the pH of precipitation. The simulated patterns are compared with observations. Weaknesses in these estimates resulting from lack of knowledge of emissions, chemical transformations and removal processes are emphasized and discussed. We also show examples of how the models can be used to estimate past and future deposition patterns. In particular, we use the IPCC scenario IS92a to estimate the possible sulfur deposition around the world in the year 2050. A comparison with critical load values for sulfur deposition indicates that substantial parts of South and East Asia are at risk for acidification problems in the future.

Source function estimate by means of variational data assimilation applied to the ETEX-I tracer experiment

The ETEX data set opens new possibilities to develop data assimilation procedures in the area of long-range transport. This paper illustrates the possibilities using a variational approach, where the source term for ETEX-I was reconstructed. The MATCH model (Robertson et al., 1996) has been the basis for this attempt. The timing of the derived emission rates are in accordance with the time period for the ETEX-I release, and a cross validation, with observations beyond the selected assimilation period, shows that the source term gained holds for the entire ETEX-I experiment. A poor-man variational approach was shown to perform nearly as good as a fully variational data assimilation. The issue of quality control has not been considered in this attempt but will be an important part that has to be addressed in future work.

Impact of climate change on ozone-related mortality and morbidity in Europe.

Ozone is a highly oxidative pollutant formed from precursors in the presence of sunlight, associated with respiratory morbidity and mortality. All else being equal, concentrations of ground-level ozone are expected to increase due to climate change. Ozone-related health impacts under a changing climate are projected using emission scenarios, models and epidemiological data. European ozone concentrations are modelled with the model of atmospheric transport and chemistry (MATCH)-RCA3 (50×50 km). Projections from two climate models, ECHAM4 and HadCM3, are applied under greenhouse gas emission scenarios A2 and A1B, respectively. We applied a European-wide exposure–response function to gridded population data and country-specific baseline mortality and morbidity. Comparing the current situation (1990–2009) with the baseline period (1961–1990), the largest increase in ozone-associated mortality and morbidity due to climate change (4–5%) have occurred in Belgium, Ireland, the Netherlands and the UK. Comparing the baseline period and the future periods (2021–2050 and 2041–2060), much larger increases in ozone-related mortality and morbidity are projected for Belgium, France, Spain and Portugal, with the impact being stronger using the climate projection from ECHAM4 (A2). However, in Nordic and Baltic countries the same magnitude of decrease is projected. The current study suggests that projected effects of climate change on ozone concentrations could differentially influence mortality and morbidity across Europe.

Validation of the operational emergency response model at the Swedish Meteorological and Hydrological Institute using data from ETEX and the Chernobyl accident

Abstract The Eulerian atmospheric tracer transport model MATCH (Multiscale Atmospheric Transport and Chemistry model) has been extended with a Lagrangian particle model treating the initial dispersion of pollutants from point sources. The model has been implemented at the Swedish Meteorological and Hydrological Institute in an emergency response system for nuclear accidents and can be activated on short notice to provide forecast concentration and deposition fields. The model has been used to simulate the transport of the inert tracer released during the ETEX experiment and the transport and deposition of 137Cs from the Chernobyl accident. Visual inspection of the results as well as statistical analysis shows that the extent, time of arrival and duration of the tracer cloud, is in good agreement with the observations for both cases, with a tendency towards over-prediction for the first ETEX release. For the Chernobyl case the simulated deposition pattern over Scandinavia and over Europe as a whole agrees with observations when observed precipitation is used in the simulation. When model calculated precipitation is used, the quality of the simulation is reduced significantly and the model fails to predict major features of the observed deposition field.

European Abatement of Surface Ozone in a Global Perspective

Abstract EUs programme Clean Air for Europe (CAFE) is presently revising the policy on air quality which will lead to the adoption of a thematic strategy on air pollution under the Sixth Environmental Action Programme by mid-2005. For the abatement of surface ozone it is becoming evident that processes outside European control will be crucial for meeting long-term aims and air quality guidelines in Europe in the future. Measurements and modelling results indicate that there is a strong link between climate change and surface ozone. A warmer and dryer European climate is very likely to lead to increased ozone concentrations. Furthermore, increased anthropogenic emissions in developing economies in Asia are likely to raise the hemispheric background level of ozone. A significant increase in the background concentration of ozone has been observed at several sites in Northern Europe although the underlying causes are not settled. The photochemical formation of tropospheric ozone from increased concentrations of methane and CO may also lead to a higher ozone level on a global scale. Gradually, these effects may outweigh the effect of the reduced European ozone precursor emissions. This calls for a global or hemispheric perspective in the revision of the European air quality policy for ozone.

Biomass burning influence on high-latitude tropospheric ozone and reactive nitrogen in summer 2008: a multi-model analysis based on POLMIP simulations

Abstract. We have evaluated tropospheric ozone enhancement in air dominated by biomass burning emissions at high latitudes (> 50° N) in July 2008, using 10 global chemical transport model simulations from the POLMIP multi-model comparison exercise. In model air masses dominated by fire emissions, ΔO3/ΔCO values ranged between 0.039 and 0.196 ppbv ppbv−1 (mean: 0.113 ppbv ppbv−1) in freshly fire-influenced air, and between 0.140 and 0.261 ppbv ppbv−1 (mean: 0.193 ppbv) in more aged fire-influenced air. These values are in broad agreement with the range of observational estimates from the literature. Model ΔPAN/ΔCO enhancement ratios show distinct groupings according to the meteorological data used to drive the models. ECMWF-forced models produce larger ΔPAN/ΔCO values (4.47 to 7.00 pptv ppbv−1) than GEOS5-forced models (1.87 to 3.28 pptv ppbv−1), which we show is likely linked to differences in efficiency of vertical transport during poleward export from mid-latitude source regions. Simulations of a large plume of biomass burning and anthropogenic emissions exported from towards the Arctic using a Lagrangian chemical transport model show that 4-day net ozone change in the plume is sensitive to differences in plume chemical composition and plume vertical position among the POLMIP models. In particular, Arctic ozone evolution in the plume is highly sensitive to initial concentrations of PAN, as well as oxygenated VOCs (acetone, acetaldehyde), due to their role in producing the peroxyacetyl radical PAN precursor. Vertical displacement is also important due to its effects on the stability of PAN, and subsequent effect on NOx abundance. In plumes where net ozone production is limited, we find that the lifetime of ozone in the plume is sensitive to hydrogen peroxide loading, due to the production of HOx from peroxide photolysis, and the key role of HO2 + O3 in controlling ozone loss. Overall, our results suggest that emissions from biomass burning lead to large-scale photochemical enhancement in high-latitude tropospheric ozone during summer.

Simulations of future sulphur and nitrogen deposition over Europe using meteorological data from three regional climate projections

We use a regional model of atmospheric chemistry and transport to investigate trends in sulphur and nitrogen deposition over Europe during the first half of the 21st century. To assess changes due to climate change, the model was operated with meteorology from a regional climate model simulating present and future climates. The sensitivity of the deposition calculations to uncertainties in the climate projections was explored by using output from three different climate models. Changes in anthropogenic air pollution emissions in Europe were extracted from the gridded RCP4.5 emission inventory. The modelling systems were evaluated by comparing average modelled precipitation, deposition and concentrations over a 20-year period with observations collected around the year 2000. We conclude that the deposition of sulphur and nitrogen containing species will mainly be governed by changes in European emissions of these species over the period 2000–2050. If future emissions follow the pathway of the RCP4.5 scenario, Europe can expect significantly lower deposition of sulphur and oxidised nitrogen in 2050 compared to 2000. For reduced nitrogen, large areas of western Europe will receive considerably more deposition in 2050 than in 2000, due to feedback of decreased sulphur concentrations on the atmospheric turnover time of reduced nitrogen. Domain averaged reductions of total deposition from 2000 to 2050 are 63, 41 and 0.9% for sulphur, oxidised- and reduced nitrogen, respectively. Climate change results in decreased wet deposition of sulphur and reduced nitrogen leading to increased atmospheric turnover time of these species. Climate and emission changes lead to decreased atmospheric turnover times of reduced nitrogen but increased atmospheric turnover times of sulphur and oxidised nitrogen. These relations are likely leading to altered source-receptor relations in the future.