Abstract
Predictions of cloud droplet activation in the late summertime (September) central Arctic Ocean are made using κ-Kohler theory with novel observations of the aerosol chemical composition from a high-resolution time-of-flight chemical ionization mass spectrometer with a filter inlet for gases and aerosols (FIGAERO-CIMS) and an aerosol mass spectrometer (AMS), deployed during the Arctic Ocean 2018 expedition onboard the Swedish icebreaker Oden. We find that the hygroscopicity parameter κ of the total aerosol is 0.39 ± 0.19 (mean ± std). The predicted activation diameter of ∼25 to 130 nm particles is overestimated by 5%, leading to an underestimation of the cloud condensation nuclei (CCN) number concentration by 4-8%. From this, we conclude that the aerosol in the High Arctic late summer is acidic and therefore highly cloud active, with a substantial CCN contribution from Aitken mode particles. Variability in the predicted activation diameter is addressed mainly as a result of uncertainties in the aerosol size distribution measurements. The organic κ was on average 0.13, close to the commonly assumed κ of 0.1, and therefore did not significantly influence the predictions. These conclusions are supported by laboratory experiments of the activation potential of seven organic compounds selected as representative of the measured aerosol.
| Original language | English |
|---|---|
| Pages (from-to) | 13888-13899 |
| Number of pages | 12 |
| Journal | Environmental Science and Technology |
| Volume | 56 |
| Issue number | 19 |
| DOIs | |
| Publication status | Published - 2022 Oct 4 |
Subject classification (UKÄ)
- Meteorology and Atmospheric Sciences
Free keywords
- aerosol chemistry
- aerosol-cloud interactions
- atmospheric aerosol
- CCN closure
- chemical ionization mass spectrometry (CIMS)
- cloud droplet activation
- High Arctic