The production, size, and chemical composition of sea spray aerosol (SSA) particles strongly depend on seawater chemistry, which is controlled by physical, chemical, and biological processes. Despite decades of studies in marine environments, a direct relationship has yet to be established between ocean biology and the physicochemical properties of SSA. The ability to establish such relationships is hindered by the fact that SSA measurements are typically dominated by overwhelming background aerosol concentrations even in remote marine environments. Herein, we describe a newly developed approach for reproducing the chemical complexity of SSA in a laboratory setting, comprising a unique ocean-atmosphere facility equipped with actual breaking waves. A mesocosm experiment was performed in natural seawater, using controlled phytoplankton and heterotrophic bacteria concentrations, which showed SSA size and chemical mixing state are acutely sensitive to the aerosol production mechanism, as well as to the type of biological species present. The largest reduction in the hygroscopicity of SSA occurred as heterotrophic bacteria concentrations increased, whereas phytoplankton and chlorophyll-a concentrations decreased, directly corresponding to a change in mixing state in the smallest (60-180 nm) size range. Using this newly developed approach to generate realistic SSA, systematic studies can now be performed to advance our fundamental understanding of the impact of ocean biology on SSA chemical mixing state, heterogeneous reactivity, and the resulting climaterelevant properties.clouds | marine aerosols | biologically active | cloud condensation nuclei | ice nucleation

Atmospheric particulate matter plays an important role in the Earth's radiative balance. Over the past two decades, it has been established that a portion of particulate matter, black carbon, absorbs significant amounts of light and exerts a warming e ect rivalling that of anthropogenic carbon dioxide 1,2 . Most climate models treat black carbon as the sole light-absorbing carbonaceous particulate. However, some organic aerosols, dubbed brown carbon and mainly associated with biomass burning emissions 3-6 , also absorbs light 7 . Unlike black carbon, whose light absorption properties are well understood 8 , brown carbon comprises a wide range of poorly characterized compounds that exhibit highly variable absorptivities, with reported values spanning two orders of magnitude 3-6,9,10 . Here we present smog chamber experiments to characterize the e ective absorptivity of organic aerosol from biomass burning under a range of conditions. We show that brown carbon in emissions from biomass burning is associated mostly with organic compounds of extremely low volatility 11 . In addition, we find that the e ective absorptivity of organic aerosol in biomass burning emissions can be parameterized as a function of the ratio of black carbon to organic aerosol, indicating that aerosol absorptivity depends largely on burn conditions, not fuel type. We conclude that brown carbon from biomass burning can be an important factor in aerosol radiative forcing.Black carbon (BC) in atmospheric particulate matter is an important global warming agent (potentially second only to CO 2 ) with estimates of its direct radiative forcing (DRF) ranging between 0.17 and 1.48 W m −2 (ref. 2). The large uncertainty in BC DRF stems partly from the mismatch between BC light absorption (hence its DRF) estimated by climate models and that retrieved using remote sensing, with models usually reporting smaller values 2 . Open biomass burning contributes one-third of the global BC budget. Biomass burning is also a major source of organic aerosol (OA), contributing two-thirds of the global primary OA budget 2,12 , which most climate models treat as purely scattering. The cooling due to this scattering offsets the warming by BC from biomass burning, resulting in negative net DRF for biomass burning emissions 13 . However, there is a growing body of evidence that biomass burning OA contains substantial amounts of light-absorbing brown carbon 3-6 (BrC), which can shift the net biomass burning DRF to positive values 14 . Neglecting absorption by biomass burning OA might lead to misattribution of observed atmospheric particulate matter absorption to BC, contributing to the discrepancy between models and observations. There are substantial uncertainties in quantifying the effect of BrC. A major obstacle is the very high variability in reported light absorption properties of biomass burning OA, often attributed to fuel type and burn conditions 4,6 , which complicates their treatment in climate models.In this study, we show that the least volatile fraction (extreme...

Ice nucleating particles (INPs) are vital for ice initiation in, and precipitation from, mixed-phase clouds. A source of INPs from oceans within sea spray aerosol (SSA) emissions has been suggested in previous studies but remained unconfirmed. Here, we show that INPs are emitted using real wave breaking in a laboratory flume to produce SSA. The number concentrations of INPs from laboratorygenerated SSA, when normalized to typical total aerosol number concentrations in the marine boundary layer, agree well with measurements from diverse regions over the oceans. Data in the present study are also in accord with previously published INP measurements made over remote ocean regions. INP number concentrations active within liquid water droplets increase exponentially in number with a decrease in temperature below 0°C, averaging an order of magnitude increase per 5°C interval. The plausibility of a strong increase in SSA INP emissions in association with phytoplankton blooms is also shown in laboratory simulations. Nevertheless, INP number concentrations, or active site densities approximated using "dry" geometric SSA surface areas, are a few orders of magnitude lower than corresponding concentrations or site densities in the surface boundary layer over continental regions. These findings have important implications for cloud radiative forcing and precipitation within low-level and midlevel marine clouds unaffected by continental INP sources, such as may occur over the Southern Ocean.marine aerosols | ice nucleation | clouds

Winter storms in California's Sierra Nevada increase seasonal snowpack and provide critical water resources and hydropower for the state. Thus, the mechanisms influencing precipitation in this region have been the subject of research for decades. Previous studies suggest Asian dust enhances cloud ice and precipitation, whereas few studies consider biological aerosols as an important global source of ice nuclei (IN). Here, we show that dust and biological aerosols transported from as far as the Sahara were present in glaciated high-altitude clouds coincident with elevated IN concentrations and ice-induced precipitation. This study presents the first direct cloud and precipitation measurements showing that Saharan and Asian dust and biological aerosols probably serve as IN and play an important role in orographic precipitation processes over the western United States.

Abstract. Data from both laboratory studies and atmospheric measurements are used to develop an empirical parameterization for the immersion freezing activity of natural mineral dust particles. Measurements made with the Colorado State University (CSU) continuous flow diffusion chamber (CFDC) when processing mineral dust aerosols at a nominal 105 % relative humidity with respect to water (RH w ) are taken as a measure of the immersion freezing nucleation activity of particles. Ice active frozen fractions vs. temperature for dusts representative of Saharan and Asian desert sources were consistent with similar measurements in atmospheric dust plumes for a limited set of comparisons available. The parameterization developed follows the form of one suggested previously for atmospheric particles of nonspecific composition in quantifying ice nucleating particle concentrations as functions of temperature and the total number concentration of particles larger than 0.5 µm diameter. Such an approach does not explicitly account for surface area and time dependencies for ice nucleation, but sufficiently encapsulates the activation properties for potential use in regional and global modeling simulations, and possible application in developing remote sensing retrievals for ice nucleating particles. A calibration factor is introduced to account for the apparent underestimate (by approximately 3, on average) of the immersion freezing fraction of mineral dust particles for CSU CFDC data processed at an RH w of 105 % vs. maximum fractions active at higher RH w . Instrumental factors that affect activation behavior vs. RH w in CFDC instruments remain to be fully explored in future studies. Nevertheless, the use of this calibration factor is supported by comparison to ice activation data obtained for the same aerosols from Aerosol Interactions and Dynamics of the Atmosphere (AIDA) expansion chamber cloud parcel experiments. Further comparison of the new parameterization, including calibration correction, to predictions of the immersion freezing surface active site density parameterization for mineral dust particles, developed separately from AIDA experimental data alone, shows excellent agreement for data collected in a descent through a Saharan aerosol layer. These studies support the utility of laboratory measurements to obtain atmospherically relevant data on the ice nucleation properties of dust and other particle types, and suggest the suitability of considering all mineral dust as a single type of ice nucleating particle as a useful first-order approximation in numerical modeling investigations.Published by Copernicus Publications on behalf of the European Geosciences Union.