Differentiation of coarse-mode anthropogenic, marine and dust\nparticles in the high Arctic Islands of Svalbard

Abstract

Abstract. Understanding aerosol-cloud-climate interactions in the Arctic is key to predict the climate in this rapidly changing region. Whilst many studies have focused on submicron aerosol (diameter less than 1\u2009μm), relatively little is known about the climate relevance of supermicron aerosol (diameter above 1\u2009μm). Here, we present a cluster analysis of multiyear (2015–2019) aerodynamic volume size distributions with diameter ranging from 0.5 to 20\u2009μm measured continuously at the Gruvebadet Observatory in the Svalbard archipelago. Together with aerosol chemical composition data from several online and offline measurements, we apportioned the occurrence of the coarse-mode aerosols to anthropogenic (two sources, 27\u2009%) and natural (three sources, 73\u2009%) origins. Specifically, two clusters are related to Arctic haze with high levels of black carbon, sulfate and accumulation mode (0.1–1\u2009μm) aerosol. The first cluster (9\u2009%) is attributed to ammonium sulfate-rich Arctic haze particles, whereas the second one (18\u2009%) to larger-mode aerosol mixed with sea salt. The three natural aerosol clusters were: open ocean sea spray aerosol (34\u2009%), mineral dust (7\u2009%), and an unidentified source of sea spray-related aerosol (32\u2009%). The results suggest that sea spray-related aerosol in polar regions may be more complex than previously thought due to short/long-distance origins and mixtures with Arctic haze, biogenic and likely snow-blowing aerosols. Studying supermicron natural aerosol in the Arctic is imperative for understanding the impacts of changing natural processes on Arctic aerosol.\n