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Clouds containing supercooled water are important for both climate and weather, but our knowledge of which aerosol particle types nucleate ice in these clouds is far from complete. Combustion aerosols have strong anthropogenic sources, and if these aerosol types were to nucleate ice in clouds, they might exert a climate forcing. Here, we quantified the atmospheric ice‐nucleating particle (INP) concentrations during the United Kingdom's annual Bonfire Night celebrations, which are characterized by large amounts of combustion aerosol from bonfires and fireworks. We used three immersion mode techniques covering more than 6 orders of magnitude in INP concentration over the temperature range from −10°C to homogeneous freezing. We found no observable systematic change in the INP concentration on three separate nights, despite more than a factor of 10 increase in aerosol number concentrations, up to a factor of 10 increase in PM10 concentration, and more than a factor of 100 increase in black carbon (BC) mass concentration relative to pre‐event levels. This implies that BC and other combustion aerosol such as ash did not compete with the INPs present in the background air. Furthermore, the upper limit of the ice‐active site surface density, ns(T), of BC generated in these events was shown to be consistent with several other recent laboratory studies, showing a very low ice‐nucleating activity of BC. We conclude that combustion aerosol particles similar to those emitted on Bonfire Night are at most of secondary importance for the INP population relevant for mixed‐phase clouds in typical midlatitude terrestrial locations. Plain Language Summary: Liquid water droplets found in clouds can cool to well below 0°C while remaining in the liquid phase (this is known as supercooling). These supercooled droplets can remain liquid down to below around −33°C without freezing, unless there is a certain type of aerosol particle present: an ice‐nucleating particle (INP). Hence, INPs have the potential to drastically change the properties and lifetime of clouds, but the sources of INP in the atmosphere are poorly defined. In this study we measured the INP concentration before, during, and after a major combustion aerosol event in the United Kingdom, Bonfire Night. This celebration is characterized by bonfires (primarily made of waste wood, but also containing garden and household waste) and fireworks. We found that aerosol particles emitted during the celebration are not as effective at nucleating ice as aerosol particle already present in the atmosphere. We conclude that aerosol particles emitted from combustion processes such as those observed on Bonfire Night are not an important source of INPs. Key Points: Ice‐nucleating particle concentrations were unaffected by high aerosol loading during Bonfire Night celebrationsAerosol concentrations rose by up to a factor of 10 and black carbon by up to a factor of 100 during these bonfire and firework eventsOur limiting active site density for Bonfire Night black carbon is consistent with other recent work with low ice‐nucleating activities [ABSTRACT FROM AUTHOR]

Abstract: Desert dust is one of the most important atmospheric ice‐nucleating aerosol species around the globe. However, there have been very few measurements of ice‐nucleating particle (INP) concentrations in dusty air close to desert sources. In this study we report the concentration of INPs in dust laden air over the tropical Atlantic within a few days' transport of one of the world's most important atmospheric sources of desert dust, the Sahara. These measurements were performed as part of the Ice in Clouds Experiment‐Dust campaign based in Cape Verde, during August 2015. INP concentrations active in the immersion mode, determined using a droplet‐on‐filter technique, ranged from around 102 m−3 at −12°C to around 105 m−3 at −23°C. There is about 2 orders of magnitude variability in INP concentration for a particular temperature, which is determined largely by the variability in atmospheric dust loading. These measurements were made at altitudes from 30 to 3,500 m in air containing a range of dust loadings. The ice active site density (ns) for desert dust dominated aerosol derived from our measurements agrees with several laboratory‐based parameterizations for ice nucleation by desert dust within 1 to 2 orders of magnitude. The small variability in ns values determined from our measurements (within about 1 order of magnitude) is striking given that the back trajectory analysis suggests that the sources of dust were geographically diverse. This is consistent with previous work, which indicates that desert dust's ice‐nucleating activity is only weakly dependent on source. [ABSTRACT FROM AUTHOR]