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Activity concentration data from ambient radioxenon measurements in ground level air, which were carried out in Europe in the framework of the International Noble Gas Experiment (INGE) in support of the development and build-up of a radioxenon monitoring network for the Comprehensive Nuclear-Test-Ban Treaty verification regime are presented and discussed. Six measurement stations provided data from 5 years of measurements performed between 2003 and 2008: Longyearbyen (Spitsbergen, Norway), Stockholm (Sweden), Dubna (Russian Federation), Schauinsland Mountain (Germany), Bruyères-le-Châtel and Marseille (both France). The noble gas systems used within the INGE are designed to continuously measure low concentrations of the four radioxenon isotopes which are most relevant for detection of nuclear explosions: 131mXe, 133mXe, 133Xe and 135Xe with a time resolution less than or equal to 24 h and a minimum detectable concentration of 133Xe less than 1 mBq/m3. This European cluster of six stations is particularly interesting because it is highly influenced by a high density of nuclear power reactors and some radiopharmaceutical production facilities. The activity concentrations at the European INGE stations are studied to characterise the influence of civilian releases, to be able to distinguish them from possible nuclear explosions. It was found that the mean activity concentration of the most frequently detected isotope, 133Xe, was 5–20 mBq/m3 within Central Europe where most nuclear installations are situated (Bruyères-le-Châtel and Schauinsland), 1.4–2.4 mBq/m3 just outside that region (Stockholm, Dubna and Marseille) and 0.2 mBq/m3 in the remote polar station of Spitsbergen. No seasonal trends could be observed from the data. Two interesting events have been examined and their source regions have been identified using atmospheric backtracking methods that deploy Lagrangian particle dispersion modelling and inversion techniques. The results are consistent with known releases of a radiopharmaceutical facility. [ABSTRACT FROM AUTHOR]

The noble gas isotope composition of the mantle can provide unique insights into the origin and evolution of volatile elements on Earth. Xenon isotopes combine primordial signatures with contributions from extinct and extant radionuclides, therefore offering the potential to set constraints on both the nature of Earth's planetary precursor(s) and the timing of their contributions. However, measuring the Xe isotope composition of mantle-derived samples to sufficiently high-precision has proven difficult due to (i) large occurrence of a modern-like atmospheric component in the mantle, and (ii) contribution from shallow and post-eruptive atmospheric contamination. Mantle-derived samples therefore exhibit only small deviations from the modern atmospheric composition, making the identification and deconvolution of mantle-derived Xe signals challenging. Here, we use the Giggenbach sampling method to concentrate magmatic noble gases from the Eifel volcanic area (Germany) into glass bottles in order to conduct high-precision analyses of Ne, Ar and Xe isotopes. The three samples collected from Victoriaquelle and Schwefelquelle wells (South East Eifel) show variable contributions from atmospheric contamination, with the least contaminated sample reaching 40Ar/36Ar ∼8,300. Our data indicate that the mantle beneath the Eifel volcanic area, and by extension the Central European Volcanic Province, resembles the convective upper mantle reservoir with limited evidence for an OIB-like deep plume source contribution. It has a geochemical signature that is similar (e.g. in Ne isotopic composition, 40Ar/36Ar, 129Xe/130Xe and 129Xe/136Xe) to the mantle source of the so-called popping rocks (thought to best represent the upper mantle), with an additional source of 238U-derived Xe and low 3He/4He that we attribute to the influence of an ancient subducted component (HIMU). A dichotomy exists between the main sources of fissiogenic xenon isotopes measured in popping rocks and Eifel gas, which appear to be mainly derived from 244Pu and 238U, respectively. According to their respective ratios of 244Pu- to 238U-derived Xe, the mantle sources for Eifel volcanism and popping rocks would have experienced extensive and limited degassing, respectively. In this regard, high Pu–Xe/(Pu+U)–Xe may no longer be considered as being indicative of a mantle deep origin, therefore calling for the geochemical differences between plume and MORB sources to be redefined, with the possibility that volatile signatures within the solid Earth may be more heterogeneously distributed than previously thought. • The mantle beneath Europe has a geochemical signature similar to MORB source mantle. • U-derived fissiogenic excesses in Eifel Xe require contribution from HIMU-like source. • The MORB reservoir exhibits extremely variable Pu–Xe/(Pu+U)–Xe. • Xenon fissiogenic excesses cannot discriminate the source of volcanism (MORB or OIB). [ABSTRACT FROM AUTHOR]