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Aerosols play a key role in Arctic warming via radiative direct and indirect effects. It is well-known that increased aerosol concentration due to Arctic haze raises cloud longwave emissivity, resulting in surface warming. Recently, a MOSAiC study demonstrated that blowing snow above sea ice generates fine sea salt aerosol, which results in up to tenfold enhancement of cloud condensation nuclei leading to potentially significant surface warming rivalling that due to Arctic haze. Yet, radiative properties of aerosol emitted by sea ice sources, vertical coupling and interaction with clouds remain major uncertainties in quantifying the aerosol impact on Arctic climate change.We use MOSAiC observations to analyse the coupled ocean-ice/snow-atmosphere system and assess contributions of sea ice sources (blowing snow, open leads) to atmospheric cloud-forming particles in particular ice-nucleating particles (INP). Choosing the 2020 winter/spring transition with profound seasonal changes in sea ice and air mass origin, we discuss the importance of sea ice aerosol to low-level clouds in comparison to advected aerosol. We consider measurements of snow particles, physico-chemical properties and INP content of aerosol and snow on sea ice, vertical profiles linking ground observations to the level of cloud formation, and assess climate sensitivity using the UKESM model.