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Discussion papers
https://doi.org/10.5194/acp-2019-427
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-2019-427
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.

Research article 16 May 2019

Research article | 16 May 2019

Review status
This discussion paper is a preprint. It is a manuscript under review for the journal Atmospheric Chemistry and Physics (ACP).

Photomineralization mechanism changes the ability of dissolved organic matter to activate cloud droplets and to nucleate ice crystals

Nadine Borduas-Dedekind1,2, Rachele Ossola1, Robert O. David2, Lin S. Boynton1, Vera Weichlinger2, Zamin A. Kanji2, and Kristopher McNeill1 Nadine Borduas-Dedekind et al.
  • 1Institute for Biogeochemistry and Pollutant Dynamics, ETH Zurich, Zurich, 8092, Switzerland
  • 2Institute for Atmospheric and Climate Sciences, ETH Zurich, Zurich, 8092, Switzerland

Abstract. An organic aerosol particle has a lifetime of approximately one week in the atmosphere during which it will be exposed to sunlight. Yet, the effect of photochemistry on the propensity of organic matter to participate in the initial cloud-forming steps is difficult to predict. In this study, we quantify on a molecular scale the effect of photochemical exposure of naturally occurring dissolved organic matter (DOM) and of a fulvic acid standard on its ability to form mixed-phase clouds, by acting as cloud condensation nuclei (CCN) and by acting as ice nucleating particles (INPs). We find that photochemical processing, equivalent to 4.6 days in the atmosphere, of DOM increases its ability to form cloud droplets by up to a factor of 2.5 but decreases its ability to form ice crystals at a loss rate of −0.04°CT50 h−1 of sunlight at ground level. In other words, the ice nucleation activity of photooxidized DOM can require up to 4 degrees colder temperatures for 50 % of the droplets to activate as ice crystals under immersion freezing conditions. This temperature change could impact the ratio of ice to water droplets within a mixed phase cloud by delaying the onset of glaciation and by increasing the supercooled liquid fraction of the cloud, thereby modifying the radiative properties and the lifetime of the cloud. Concurrently, a photomineralization mechanism was quantified by monitoring the loss of organic carbon and the simultaneous production of organic acids, such as formic, acetic, oxalic and pyruvic acids, CO and CO2. This mechanism explains and predicts the observed increase in CCN and decrease in INP efficiencies. Indeed, we show that photochemical processing can be a dominant atmospheric aging process, impacting CCN and INP efficiencies and concentrations. Photomineralization can thus alter the aerosol-cloud radiative effects of organic matter by modifying the supercooled liquid water-to-ice crystal ratio in mixed-phase clouds with implications for cloud lifetime, precipitation patterns and the hydrological cycle.

Nadine Borduas-Dedekind et al.
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Photomineralization mechanism changes the ability of dissolved organic matter to activate cloud droplets and to nucleate ice crystals N. Borduas-Dedekind https://doi.org/10.3929/ethz-b-000342107

Nadine Borduas-Dedekind et al.
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Short summary
During atmospheric transport, dissolved organic matter (DOM) within aqueous aerosols undergoes photochemistry. We find that photochemical processing of DOM increases its ability to form cloud droplets but decreases its ability to form ice crystals over a simulated 4.6 days in the atmosphere. A photomineralization mechanism involving the loss of organic carbon and the production of organic acids, CO and CO2 explains the observed changes and affects the liquid water to ice ratio in clouds.
During atmospheric transport, dissolved organic matter (DOM) within aqueous aerosols undergoes...
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