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The European Union (EU)-funded project Dynamics–Aerosol–Chemistry–Cloud Interactions in West Africa (DACCIWA) investigates the relationship between weather, climate, and air pollution in southern West Africa—an area with rapid population growth, urbanization, and an increase in anthropogenic aerosol emissions. The air over this region contains a unique mixture of natural and anthropogenic gases, liquid droplets, and particles, emitted in an environment in which multilayer clouds frequently form. These exert a large influence on the local weather and climate, mainly owing to their impact on radiation, the surface energy balance, and thus the diurnal cycle of the atmospheric boundary layer. In June and July 2016, DACCIWA organized a major international field campaign in Ivory Coast, Ghana, Togo, Benin, and Nigeria. Three supersites in Kumasi, Savè, and Ile-Ife conducted permanent measurements and 15 intensive observation periods. Three European aircraft together flew 50 research flights between 27 June and 16 July 2016, for a total of 155 h. DACCIWA scientists launched weather balloons several times a day across the region (772 in total), measured urban emissions, and evaluated health data. The main objective was to build robust statistics of atmospheric composition, dynamics, and low-level cloud properties in various chemical landscapes to investigate their mutual interactions. This article presents an overview of the DACCIWA field campaign activities as well as some first research highlights. The rich data obtained during the campaign will be made available to the scientific community and help to advance scientific understanding, modeling, and monitoring of the atmosphere over southern West Africa.

The isotopic composition of molecular hydrogen (H₂) contains independent information for constraining the global H₂ budget. To explore this, we have implemented hydrogen sources and sinks, including their stable isotopic composition and isotope fractionation constants, into the global chemistry transport model TM5. For the first time, a global model now includes a simplified but explicit isotope reaction scheme for the photochemical production of H₂. We present a comparison of modelled results for the H₂ mixing ratio and isotope composition with available measurements on seasonal to inter annual time scales for the years 2001–2007. The base model results agree well with observations for H₂ mixing ratios. For δD[H₂], modelled values are slightly lower than measurements. A detailed sensitivity study is performed to identify the most important parameters for modelling the isotopic composition of H₂. The results show that on the global scale, the discrepancy between model and measurements can be closed by adjusting the default values of the isotope effects in deposition, photochemistry and the stratosphere-troposphere exchange within the known range of uncertainty. However, the available isotope data do not provide sufficient information to uniquely constrain the global isotope budget. Therefore, additional studies focussing on the isotopic composition near the tropopause and on the isotope effects in the photochemistry and deposition are recommended