Four Years of Active Sampling and Measurement of Atmospheric Polycyclic Aromatic Hydrocarbons and Oxygenated Polycyclic Aromatic Hydrocarbons in Dronning Maud Land, East Antarctica.

Antarctica, protected by its strong polar vortex and sheer distance from anthropogenic activity, was always thought of as pristine. However, as more data on the occurrence of persistent organic pollutants on Antarctica emerge, the question arises of how fast the long-range atmospheric transport takes place. Therefore, polycyclic aromatic hydrocarbons (PAHs) and oxygenated (oxy-)PAHs were sampled from the atmosphere and measured during 4 austral summers from 2017 to 2021 at the Princess Elisabeth station in East Antarctica. The location is suited for this research as it is isolated from other stations and activities, and the local pollution of the station itself is limited. A high-volume sampler was used to collect the gas and particle phase (PM10) separately. Fifteen PAHs and 12 oxy-PAHs were quantified, and concentrations ranging between 6.34 and 131 pg m3 (Σ15PAHs-excluding naphthalene) and between 18.8 and 114 pg m3 (Σ13oxy-PAHs) were found. Phenanthrene, pyrene, and fluoranthene were the most abundant PAHs. The gas-particle partitioning coefficient log(Kp) was determined for 6 compounds and was found to lie between 0.5 and -2.5. Positive matrix factorization modeling was applied to the data set to determine the contribution of different sources to the observed concentrations. A 6-factor model proved a good fit to the data set and showed strong variations in the contribution of different air masses. During the sampling campaign, a number of volcanic eruptions occurred in the southern hemisphere from which the emission plume was detected. The FLEXPART dispersion model was used to confirm that the recorded signal is indeed influenced by volcanic eruptions. The data was used to derive a transport time of between 11 and 33 days from release to arrival at the measurement site on Antarctica.

A baseline for source localisation using the inverse modelling tool FREAR.

A global network of monitoring stations is set up that can measure tiny concentrations of airborne radioactivity as part of the verification regime of the Comprehensive Nuclear-Test-Ban Treaty. If Treaty-relevant detections are made, inverse atmospheric transport modelling is one of the methods that can be used to determine the source of the radioactivity. In order to facilitate the testing of novel developments in inverse modelling, two sets of test cases are constructed using real-world 133Xe detections associated with routine releases from a medical isotope production facility. One set consists of 24 cases with 5 days of observations in each case, and another set consists of 8 cases with 15 days of observations in each case. A series of inverse modelling techniques and several sensitivity experiments are applied to determine the (known) location of the medical isotope production facility. Metrics are proposed to quantify the quality of the source localisation. Finally, it is illustrated how the sets of test cases can be used to test novel developments in inverse modelling algorithms.