Abstract

AbstractAs Arctic sea ice cover diminishes, sea spray aerosols (SSA) have a larger potential to be emitted into the Arctic atmosphere. Emitted SSA can contain organic material, but how it affects the ability of particles to act as cloud condensation nuclei (CCN) is still not well understood. Here we measure the CCN‐derived hygroscopicity of three different types of aerosol particles: (1) Sea salt aerosols made from artificial seawater, (2) aerosol generated from artificial seawater spiked with diatom species cultured in the laboratory, and (3) aerosols made from samples of sea surface microlayer (SML) collected during field campaigns in the North Atlantic and Arctic Ocean. Samples are aerosolized using a sea spray simulation tank (plunging jet) or an atomizer. We show that SSA containing diatom and microlayer exhibit similar CCN activity to inorganic sea salt with a κ value of ∼1.0. Large‐eddy simulation (LES) is then used to evaluate the general role of aerosol hygroscopicity in governing mixed‐phase low‐level cloud properties in the high Arctic. For accumulation mode aerosol, the simulated mixed‐phase cloud properties do not depend strongly on κ, unless the values are lower than 0.4. For Aitken mode aerosol, the hygroscopicity is more important; the particles can sustain the cloud if the hygroscopicity is equal to or higher than 0.4, but not otherwise. The experimental and model results combined suggest that the internal mixing of biogenic organic components in SSA does not have a substantial impact on the cloud droplet activation process and the cloud lifetime in Arctic mixed‐phase clouds.

Highlights

  • The Arctic region is currently warming faster than the rest of the globe (Blunden & Arndt, 2019), and as sea ice cover is diminishing (Blunden & Arndt, 2019), the effect of a potential increase in sea spray aerosol (SSA) emissions on clouds and climate calls for attention

  • We measure the cloud condensation nuclei (CCN)-derived hygroscopicity of three different types of aerosol particles: (1) Sea salt aerosols made from artificial seawater, (2) aerosol generated from artificial seawater spiked with diatom species cultured in the laboratory, and (3) aerosols made from samples of sea surface microlayer (SML) collected during field campaigns in the North Atlantic and Arctic Ocean

  • In the first part of the study, we make a comprehensive experimental evaluation of the CCN activity of three types of aerosol particles of increasing complexity: (1) Sea salt aerosols made from artificial seawater, (2) aerosol particles generated from artificial seawater spiked with diatom species cultured in the laboratory (Melosira arctica, the most abundant phytoplankton in the Arctic region, and Skeletonema marinoi, a diatom typical of temperate regions), and (3) aerosol particles made from samples of SML collected during field campaigns in the North Atlantic and Arctic Ocean

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Summary

Introduction

The Arctic region is currently warming faster than the rest of the globe (Blunden & Arndt, 2019), and as sea ice cover is diminishing (Blunden & Arndt, 2019), the effect of a potential increase in sea spray aerosol (SSA) emissions on clouds and climate calls for attention. Measurements of CCN were carried out throughout an icebreaker research expedition to the high Arctic during the biologically most active period in the summer of 2008 (Leck & Svensson, 2015; Tjernström et al, 2014). Whereas the CCN concentrations varied by 2 to 3 orders of magnitude over the expedition, occasionally below 1 cm−3, median daily CCN concentrations at 0.2% water vapor supersaturation (SS) were

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