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Oceans emit ice-nucleating particles (INPs) which freeze supercooled cloud droplets, modifying clouds. We added dead biomass of three phytoplankton to seawater. Each time, this stimulated INP production in the water and INP emissions in sea spray. 

Plastic pollution is one of the most pressing environmental and social issues of the 21st century. Recent work has highlighted the atmosphere’s role in transporting microplastics to remote locations [S. Allen et al.,Nat. Geosci.12, 339 (2019) and J. Brahney, M. Hallerud, E. Heim, M. Hahnenberger, S. Sukumaran,Science368, 1257–1260 (2020)]. Here, we use in situ observations of microplastic deposition combined with an atmospheric transport model and optimal estimation techniques to test hypotheses of the most likely sources of atmospheric plastic. Results suggest that atmospheric microplastics in the western United States are primarily derived from secondary re-emission sources including roads (84%), the ocean (11%), and agricultural soil dust (5%). Using our best estimate of plastic sources and modeled transport pathways, most continents were net importers of plastics from the marine environment, underscoring the cumulative role of legacy pollution in the atmospheric burden of plastic. This effort uses high-resolution spatial and temporal deposition data along with several hypothesized emission sources to constrain atmospheric plastic. Akin to global biogeochemical cycles, plastics now spiral around the globe with distinct atmospheric, oceanic, cryospheric, and terrestrial residence times. Though advancements have been made in the manufacture of biodegradable polymers, our data suggest that extant nonbiodegradable polymers will continue to cycle through the earth’s systems. Due to limited observations and understanding of the source processes, there remain large uncertainties in the transport, deposition, and source attribution of microplastics. Thus, we prioritize future research directions for understanding the plastic cycle. 

Abstract. Ice-nucleating particles (INPs) represent a rare subset of aerosol particlesthat initiate cloud droplet freezing at temperatures above the homogenousfreezing point of water (−38 ∘C). Considering that the oceancovers 71 % of the Earth's surface and represents a large potential sourceof INPs, it is imperative that the identities, properties and relativeemissions of ocean INPs become better understood. However, the specificunderlying drivers of marine INP emissions remain largely unknown due tolimited observations and the challenges associated with isolating rare INPs. Bygenerating isolated nascent sea spray aerosol (SSA) over a range ofbiological conditions, mesocosm studies have shown that marine microbes cancontribute to INPs. Here, we identify 14 (30 %) cultivable halotolerantice-nucleating microbes and fungi among 47 total isolates recovered fromprecipitation and aerosol samples collected in coastal air in southernCalifornia. Ice-nucleating (IN) isolates collected in coastal air were nucleated ice fromextremely warm to moderate freezing temperatures (−2.3 to −18 ∘C). While some Gammaproteobacteria and fungi are known to nucleate ice attemperatures as high as −2 ∘C, Brevibacterium sp. is the first Actinobacteriafound to be capable of ice nucleation at a relatively high freezingtemperature (−2.3 ∘C). Air mass trajectory analysis demonstratesthat marine aerosol sources were dominant during all sampling periods, andphylogenetic analysis indicates that at least 2 of the 14 IN isolates areclosely related to marine taxa. Moreover, results from cell-washingexperiments demonstrate that most IN isolates maintained freezing activityin the absence of nutrients and cell growth media. This study supportsprevious studies that implicated microbes as a potential source of marineINPs, and it additionally demonstrates links between precipitation, marineaerosol and IN microbes. 

Atmospheric rivers (ARs), and frontal systems more broadly, tend to exhibit prominent “V” shapes in time series of stable isotopes in precipitation. Despite the magnitude and widespread nature of these “V” shapes, debate persists as to whether these shifts are driven by changes in the degree of rainout, which we determine using the Rayleigh distillation of stable isotopes, or by post-condensation processes such as below-cloud evaporation and equilibrium isotope exchange between hydrometeors and surrounding vapor. Here, we present paired precipitation and water vapor isotope time series records from the 5–7 March 2016, AR in Bodega Bay, CA. The stable isotope composition of surface vapor along with independent meteorological constraints such as temperature and relative humidity reveal that rainout and post-condensation processes dominate during different portions of the event. We find that Rayleigh distillation controls during peak AR conditions (with peak rainout of 55%) while post-condensation processes have their greatest effect during periods of decreased precipitation on the margins of the event. These results and analyses inform critical questions regarding the temporal evolution of AR events and the physical processes that control them at local scales. 

Abstract. Ice nucleating particles (INP) have been found to influence the amount, phase, and efficiency of precipitation from winter storms, including atmospheric rivers. Warm INP, those that initiate freezing at temperatures warmer than −10°C, are thought to be particularly impactful because they can create primary ice in mixed-phase clouds, enhancing precipitation efficiency. The dominant sources of warm INP during atmospheric rivers, the role of meteorology in modulating transport and injection of warm INP into atmospheric river clouds and the impact of warm INP on mixed-phase cloud properties are not well-understood. Time-resolved precipitation samples were collected during an atmospheric river in Northern California, USA during winter 2016. Precipitation was collected at two sites, one coastal and one inland, that are separated by less than 35km. The sites are sufficiently close that airmass sources during this storm were almost identical, but the inland site was exposed to terrestrial sources of warm INP while the coastal site was not. Warm INP were more numerous in precipitation at the inland site by an order of magnitude. Using FLEXPART dispersion modelling and radar-derived cloud vertical structure, we detected influence from terrestrial INP sources at the inland site, but did not find clear evidence of marine warm INP at either site. We episodically detected warm INP from long-range transported sources at both sites. By extending the FLEXPART modelling using a meteorological reanalysis, we demonstrate that long-range transported warm INP are observed only when the upper tropospheric jet provided transport to cloud tops. Using radar-derived hydrometeor classifications, we demonstrate that hydrometeors over the terrestrially-influenced inland site were more likely to be in the ice phase for cloud temperatures between 0°C and −10°C. We thus conclude that terrestrial and long-range transported aerosol were important sources of warm INP during this atmospheric river. Meteorological details such as transport mechanism and cloud structure were important in determining warm INP source strength and injection temperature, and ultimately the impact of warm INP on mixed phase cloud properties. 

Abstract Oceans are, generally, relatively weak sources of ice nucleating particles (INPs). Thus, dust transported from terrestrial regions can dominate atmospheric INP concentrations even in remote marine regions. Studies of ocean‐emitted INPs have focused upon sea spray aerosols containing biogenic species. Even though large concentrations of dust are transported over marine regions, resuspended dust has never been explicitly considered as another possible source of ocean‐emitted INPs. Current models assume that deposited dust is not re‐emitted from surface waters. Our laboratory studies of aerosol particles produced from coastal seawater and synthetic seawater doped with dust show that dust can indeed be ejected from water during bubble bursting. INP concentration measurements show these ejected dust particles retain ice nucleating activity. Doping synthetic seawater to simulate a strong dust deposition event produced INPs active at temperatures colder than −13°C and INP concentrations 1 to 2 orders of magnitude greater than either lab sea spray or marine boundary layer measurements. The relevance of these laboratory findings is highlighted by single‐particle composition measurements along the Californian coast where at least 9% of dust particles were mixed with sea salt. Additionally, global modeling studies show that resuspension of dust from the ocean could exert the most impact over the Southern Ocean, where ocean‐emitted INPs are thought to dominate atmospheric INP populations. More work characterizing the factors governing the resuspension of dust particles is required to understand the potential impact upon clouds.