The role of local shipping emissions in aerosol-cloud interactions in the central Arctic

Abstract Arctic shipping is projected to increase as sea ice retreats, yet the impact of modern low-sulfur ship emissions on Arctic clouds and radiation remain poorly constrained. We use year-long in situ observations from the MOSAiC expedition to characterize ship-aerosol-cloud interactions for an icebreaker burning ultra-low sulfur fuel (0.1% mass per mass). Exhaust plumes were found to be strongly enriched in Aitken-mode particles, organic aerosol, and black carbon, but showed no detectable enhancement in particulate sulfate. Despite reduced hygroscopicity relative to ambient aerosols, ship emissions substantially increased local cloud condensation nuclei concentrations. A droplet activation parametrization was applied to quantify responses in cloud droplet number concentration (N d ) to ship-induced perturbations in low-level Arctic clouds. In winter, abundant background accumulation-mode particles from Arctic haze supplied nearly all cloud droplets, while additional particles from ship emissions had little impact on N d . In contrast, during summer months, when unperturbed background aerosol concentrations are low, ship emissions nearly doubled N d compared to average background conditions and increased N d by a factor of five compared to very clean background conditions (25 th percentile of background aerosol number concentrations). Longwave radiative transfer simulations for typical conditions of summer Arctic low-level clouds/fog suggest that these ship-induced increases in N d locally (i.e., < 100 km downwind) lead to enhanced net surface longwave fluxes and consequent warming, primarily for optically thin clouds (liquid water path (LWP) ≤ 30 g•m -2 ). For LWP = 10 g•m -2 , ship emissions lead to an increase of 1 W•m -2 in cloud longwave forcing at the surface compared to average unperturbed conditions (+ 7% relative increase), and up to 4 W•m -2 when compared to very clean background conditions (+ 22% relative increase). Even ultra-low sulfur fuel emissions can therefore locally and episodically modify Arctic cloud microphysics and radiative properties, especially during summer, implying that future increases in Arctic shipping could have non-negligible regional climate impacts.

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Publication Details

Journal
Environmental Research Letters
Published
2026-04-29
DOI
https://doi.org/10.1088/1748-9326/ae6673
Primary Topic
Atmospheric aerosols and clouds
Type
article
Field-Weighted Citation Impact
0.00

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article

The role of local shipping emissions in aerosol-cloud interactions in the central Arctic

Benjamin Heutte, Lauriane L. J. Quéléver, Nora Bergner, Ivo Beck et al.
Environmental Research Letters
Atmospheric aerosols and clouds
article

The role of local shipping emissions in aerosol-cloud interactions in the central Arctic

Benjamin Heutte, Lauriane L. J. Quéléver, Nora Bergner, Ivo Beck, Julia Schmale, Lubna Dada, Jessie Creamean, Roman Pohorsky, Athanasios Nenes, Michael Lonardi, Kerri A Pratt, Silvia Henning, Sébastien l Rogers, Tuija Beatta Aurora Jokinen, Hélène Angot, Tuukka Petäjä
article en

Abstract

Abstract Arctic shipping is projected to increase as sea ice retreats, yet the impact of modern low-sulfur ship emissions on Arctic clouds and radiation remain poorly constrained. We use year-long in situ observations from the MOSAiC expedition to characterize ship-aerosol-cloud interactions for an icebreaker burning ultra-low sulfur fuel (0.1% mass per mass). Exhaust plumes were found to be strongly enriched in Aitken-mode particles, organic aerosol, and black carbon, but showed no detectable enhancement in particulate sulfate. Despite reduced hygroscopicity relative to ambient aerosols, ship emissions substantially increased local cloud condensation nuclei concentrations. A droplet activation parametrization was applied to quantify responses in cloud droplet number concentration (N d ) to ship-induced perturbations in low-level Arctic clouds. In winter, abundant background accumulation-mode particles from Arctic haze supplied nearly all cloud droplets, while additional particles from ship emissions had little impact on N d . In contrast, during summer months, when unperturbed background aerosol concentrations are low, ship emissions nearly doubled N d compared to average background conditions and increased N d by a factor of five compared to very clean background conditions (25 th percentile of background aerosol number concentrations). Longwave radiative transfer simulations for typical conditions of summer Arctic low-level clouds/fog suggest that these ship-induced increases in N d locally (i.e., < 100 km downwind) lead to enhanced net surface longwave fluxes and consequent warming, primarily for optically thin clouds (liquid water path (LWP) ≤ 30 g•m -2 ). For LWP = 10 g•m -2 , ship emissions lead to an increase of 1 W•m -2 in cloud longwave forcing at the surface compared to average unperturbed conditions (+ 7% relative increase), and up to 4 W•m -2 when compared to very clean background conditions (+ 22% relative increase). Even ultra-low sulfur fuel emissions can therefore locally and episodically modify Arctic cloud microphysics and radiative properties, especially during summer, implying that future increases in Arctic shipping could have non-negligible regional climate impacts.

Environmental Research Letters
U.S. Department of Energy, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Swiss Polar Institute
Life below water
Openalex Percentile: Top 7%
Atmospheric aerosols and clouds
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