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Tritium is one of the most important environmental tracers in isotope hydrology for understanding the dynamics of groundwater and connected surface water and has been used in a wide range of applications at different scales. A key requirement for using tritium as a tracer is the knowledge of its spatial and temporal distribution in different water types. As a fundamental input, quantity long‐term time series of tritium in precipitation are of particular importance. In this paper, the authors present an overview of tritium data sets of the Federal Institute of Hydrology (BfG), the Helmholtz Zentrum München (HMGU) and the German Weather Service (DWD). Since the 1970s, all three institutions have monitored the tritium concentration at 53 surface water and 37 precipitation stations on a monthly basis. The primary purpose of the data set was to provide baseline information for different water types all over Germany as an integral part of the German radiation protection monitoring system. Additionally, as geochemically inert tracer, tritium provides a unique tool to different user groups in a wide range of research questions and applications.

Background The implementation of emission mitigation policies in Europe over the last two decades has generally improved the air quality, which resulted in lower aerosol particle mass, particle number, and black carbon mass concentration. However, little is known whether the decreasing particle concentrations at a lower-altitude level can be observed in the free troposphere (FT), an important layer of the atmosphere, where aerosol particles have a longer lifetime and may affect climate dynamics. In this study, we used data from two high-Alpine observatories, Zugspitze-Schneefernerhaus (ZSF) and Jungfraujoch (JFJ), to assess the long-term trends on size-resolved particle number concentrations (PNCs) and equivalent black carbon (eBC) mass concentration separated for undisturbed lower FT conditions and under the influence of air from the planetary boundary layer (PBL) from 2009 to 2018. Results The FT and PBL-influenced conditions were segregated for both sites. We found that the FT conditions in cold months were more prevalent than in warm months, while the measured aerosol parameters showed different seasonal patterns for the FT and PBL-influenced conditions. The pollutants in the PBL-influenced condition have a higher chance to be transported to high-altitudes due to the mountainous topography, leading to a higher concentration and more distinct seasonal variation, and vice versa. The long-term trends of the measured aerosol parameters were evaluated and the decreased aerosol concentrations were observed for both FT and PBL-influenced conditions. The observed decreasing trends in eBC concentration in the PBL-influenced condition are well consistent with the reported trends in total BC emission in Germany and Switzerland. The decreased concentrations in the FT condition suggest that the background aerosol concentration in the lower FT over Central Europe has correspondingly decreased. The change of back trajectories in the FT condition at ZSF and JFJ was further evaluated to investigate the other possible drivers for the decreasing trends. Conclusions The background aerosol concentration in the lower FT over Central Europe has significantly decreased during 2009–2018. The implementation of emission mitigation policies is the most decisive factor and the decrease of the regional airmass occurrence over Central Europe also has contributed to the decreasing trends.

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A single episode of pine pollen release in the highly contaminated area of Novozybkov, Russian Federation, which led to enhanced atmospheric concentrations of 137Cs is discussed. The pollen grains were sampled by a rotating arm impactor and analysed by gamma-spectrometry for 137Cs activity and by image analysis for their size. In the vicinity of a forest, a maximum concentration of 4.5+/-0.4 mBq m(-3) was measured, and a mean activity per pollen grain of 260+/-80 nBq was determined. The emission rate of the Novozybkov mixed pine forest was estimated to be approximately 400 Bq m(-2) per year. Because of the large size of pine pollen grains (about 50 microm) and the short emission period of 5-8 days per year, the estimated potential annual inhalation doses are very low. Biological emissions including pollen release may be a source of increased airborne radionuclide concentrations at larger distances from the source areas as well.