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The Arctic is warming at more than twice the rate of the global average. This warming is influenced by clouds, which modulate the solar and terrestrial radiative fluxes and, thus, determine the surface energy budget. However, the interactions among clouds, aerosols, and radiative fluxes in the Arctic are still poorly understood. To address these uncertainties, the Ny-Ålesund Aerosol Cloud Experiment (NASCENT) study was conducted from September 2019 to August 2020 in Ny-Ålesund, Svalbard. The campaign's primary goal was to elucidate the life cycle of aerosols in the Arctic and to determine how they modulate cloud properties throughout the year. In situ and remote sensing observations were taken on the ground at sea level, at a mountaintop station, and with a tethered balloon system. An overview of the meteorological and the main aerosol seasonality encountered during the NASCENT year is introduced, followed by a presentation of first scientific highlights. In particular, we present new findings on aerosol physicochemical and molecular properties. Further, the role of cloud droplet activation and ice crystal nucleation in the formation and persistence of mixed-phase clouds, and the occurrence of secondary ice processes, are discussed and compared to the representation of cloud processes within the regional Weather Research and Forecasting Model. The paper concludes with research questions that are to be addressed in upcoming NASCENT publications. [ABSTRACT FROM AUTHOR]

Laboratory generated aerosols and aerosol sampled in a field campaign were studied to assess the repeatability of heterogeneous ice activation processes and verify if the ice nuclei particles maintained their nucleating capability. Experiments were performed using a filter technique, i.e. aerosol particles were sampled on black-gridded cellulose nitrate membrane filters and assessed for ice nucleating particles in a dynamic filter-processing chamber at our ISAC-CNR laboratory. The laboratory investigations used Arizona Test Dust (ATD) generated by nebulizing a suspension of ATD. After nebulization, the wet aerosol in the carrier gas was dried and then sampled on a filter. Aerosol field sampling (size range PM1 and PM10) was carried out in the Arctic (Ny-Ålesund, Svalbard) from 12 to 23 April 2019. The activation processes were repeated twice for each filter at temperatures of −22 °C and −18 °C. For aerosol, ATD runs were performed only in conditions of supersaturation (saturation ratio S w = 1.02), while for the Arctic aerosol, conditions below saturation were also considered (S w = 0.96). The experiments showed that approximately 40% of the ATD particles maintain their initial nucleating efficiency, both at T = −22 °C and − 18 °C, and at S w = 1.02, i.e. in the condensation freezing mode. The percentage of repeatability was higher for ATD with respect to the Artic-sampled aerosol processed in the condensation mode. This may depend on greater particle morphology variation of the mixed organic-inorganic aerosol due to the hydration and dehydration cycle. • Experiments showed that about 40% of ATD particles maintains the nucleating efficacy. • The repeatability was higher for ATD with respect to aerosol sampled in Arctic. • Variation of ice nucleating capability of the aerosol has atmospheric implication. • The ice nucleation shows both stochastic and deterministic behavior. [ABSTRACT FROM AUTHOR]