Abstract: The nitrogen stable isotopic composition in nitrate (δ15N-NO−3) measured in ice cores from low-snow-accumulation regions in East Antarctica has the potential to provide constraints on past ultraviolet (UV) radiation and thereby total column ozone (TCO) due to the sensitivity of nitrate (NO−3) photolysis to UV radiation. However, understanding the transfer of reactive nitrogen at the air–snow interface in polar regions is paramount for the interpretation of ice core records of δ15N-NO−3 and NO−3 mass concentrations. As NO−3 undergoes a number of post-depositional processes before it is archived in ice cores, site-specific observations of δ15N-NO−3 and air–snow transfer modelling are necessary to understand and quantify the complex photochemical processes at play. As part of the Isotopic Constraints on Past Ozone Layer Thickness in Polar Ice (ISOL-ICE) project, we report new measurements of NO−3 mass concentration and δ15N-NO−3 in the atmosphere, skin layer (operationally defined as the top 5 mm of the snowpack), and snow pit depth profiles at Kohnen Station, Dronning Maud Land (DML), Antarctica. We compare the results to previous studies and new data, presented here, from Dome C on the East Antarctic Plateau. Additionally, we apply the conceptual 1D model of TRansfer of Atmospheric Nitrate Stable Isotopes To the Snow (TRANSITS) to assess the impact of NO−3 recycling on δ15N-NO−3 and NO−3 mass concentrations archived in snow and firn. We find clear evidence of NO−3 photolysis at DML and confirmation of previous theoretical, field, and laboratory studies that UV photolysis is driving NO−3 recycling and redistribution at DML. Firstly, strong denitrification of the snowpack is observed through the δ15N-NO−3 signature, which evolves from the enriched snowpack (−3 ‰ to 100 ‰), to the skin layer (−20 ‰ to 3 ‰), to the depleted atmosphere (−50 ‰ to −20 ‰), corresponding to mass loss of NO−3 from the snowpack. Based on the TRANSITS model, we find that NO−3 is recycled two times, on average, before it is archived in the snowpack below 15 cm and within 0.75 years (i.e. below the photic zone). Mean annual archived δ15N-NO−3 and NO−3 mass concentration values are 50 ‰ and 60 ng g−1, respectively, at the DML site. We report an e-folding depth (light attenuation) of 2–5 cm for the DML site, which is considerably lower than Dome C. A reduced photolytic loss of NO−3 at DML results in less enrichment of δ15N-NO−3 than at Dome C mainly due to the shallower e-folding depth but also due to the higher snow accumulation rate based on TRANSITS-modelled sensitivities. Even at a relatively low snow accumulation rate of 6 cm yr−1 (water equivalent; w.e.), the snow accumulation rate at DML is great enough to preserve the seasonal cycle of NO−3 mass concentration and δ15N-NO−3, in contrast to Dome C where the depth profiles are smoothed due to longer exposure of surface snow layers to incoming UV radiation before burial. TRANSITS sensitivity analysis of δ15N-NO−3 at DML highlights that the dominant factors controlling the archived δ15N-NO−3 signature are the e-folding depth and snow accumulation rate, with a smaller role from changes in the snowfall timing and TCO. Mean TRANSITS model sensitivities of archived δ15N-NO−3 at the DML site are 100 ‰ for an e-folding depth change of 8 cm, 110 ‰ for an annual snow accumulation rate change of 8.5 cm yr−1 w.e., 10 ‰ for a change in the dominant snow deposition season between winter and summer, and 10 ‰ for a TCO change of 100 DU (Dobson units). Here we set the framework for the interpretation of a 1000-year ice core record of δ15N-NO−3 from DML. Ice core δ15N-NO−3 records at DML will be less sensitive to changes in UV than at Dome C; however the higher snow accumulation rate and more accurate dating at DML allows for higher-resolution δ15N-NO−3 records.

Abstract: High southern latitude regions present specificities that are highly relevant for studying the climate in connection with the atmospheric chemistry. Contrary to regions of the rest of the world, Antarctica is still considered as a pristine environment not yet influenced by predominant anthropogenic emissions (with the notable exceptions of GHG) and thus represents the last continental-size natural laboratory. Polar snow-air-radiation interactions and the specific oxidant character of the polar atmosphere are key in order to decipher the right information buried in the ice and the current chemical stability of the polar atmosphere. Previous Antarctic campaigns have shown atmospheric similarities between the Antarctic Plateau (at Dome C, Concordia) and other regions. However, several differences are yet to be explained: the large NO2:NO ratios previously found in ambient air indicates the existence of an unknown source of NO2 above the Antarctic Plateau. These observations question either the reliability of previous measurements or the lack of our understanding of the NOx chemistry. Novel optical instruments based on the incoherent broadband cavity enhanced absorption spectroscopy technique (IBBCEAS) were developed. The instruments can measure simultaneously NO2, NOx and NO with detection limits of 11, 10 and 21 ppt, respectively (1σ) within 22 minutes of measurements. The two compact and transportable instruments were deployed during the 2019/20 Dome C summer campaign. Atmospheric measurements together with flux chamber experiments were performed for determining the snowpack NOx emissions and the NO2:NO ratio. The observations seem to differ from the conclusions of the previous Antarctic campaigns. Assuming steady state and maximum radiations, the theoretical NO2:NO ratio from the period observed in December was calculated to be 0.38 ± 0.15 and 0.31 ± 0.12 in January. The instruments measured a ratio close to steady state in December (0.25 ± 0.25) while the ratio observed in January (1.248 ± 0.792) indicates the presence of a strong NO oxidant or an unknown source of NO2. Flux chamber experiments on different types of snow were done during this campaign, and the results will help deepen our knowledge of Antarctic atmospheric chemistry.

Abstract: The objective of this contribution is to get new insights into the effects of magnetic field variations of natural and anthropogenic origin on broad-band seismic stations. Regarding natural sources of magnetic perturbations, we have investigated if the Sudden Storm Commencements (SSC) cataloged during the 24th solar cycle (2008–2019) can be systematically identified in broad-band seismic stations distributed worldwide. The results show that the 23 SSC events with a mean amplitude above 30 nT and most of those with lower energy but still clearly identified in the magnetometer detection network can be observed at broad-band stations’ network using a simple low-pass filter. Although the preliminary impulse of those signals is usually stronger at stations located at high latitudes, major SSC are observed at seismic stations distributed worldwide. Regarding anthropogenic sources, we focus on the short period seismic signals recorded in urban environments which are correlated with the activity of the railway transportation system. We have analyzed collocated measurements of electric field and seismic signals within Barcelona, evidencing that significant changes in the electric field following the activity of the transportation systems can be attributed to leakage currents transmitted to the soil by trains. During space weather events, electric currents in the magnetosphere and ionosphere experience large variations inducing telluric currents near the Earth surface, which in turn generate a secondary magnetic field. In the case of underground trains, leakage currents are transmitted to the soil, which in turn can result in local variations in the magnetic field. The observed signals in modern seismometers can be related to the reaction of the suspension springs to these magnetic field variations or to the effect of the magnetic field variations on the force transducers used to keep the mass fixed.