Abstract. The NEMS GFS Aerosol Component Version 2.0 (NGACv2) for global multispecies aerosol forecast has been developed at the National Centers of Environment Prediction (NCEP) in collaboration with the NESDIS Center for Satellite Applications and Research (STAR), the NASA Goddard Space Flight Center (GSFC), and the University at Albany, State University of New York (SUNYA). This paper describes the continuous development of the NGAC system at NCEP after the initial global dust-only forecast implementation (NGAC version 1.0, NGACv1). With NGACv2, additional sea salt, sulfate, organic carbon, and black carbon aerosol species were included. The smoke emissions are from the NESDIS STAR's Global Biomass Burning Product (GBBEPx), blended from the global biomass burning emission product from a constellation of geostationary satellites (GBBEP-Geo) and GSFC's Quick Fire Emission Data Version 2 from a polar-orbiting sensor (QFED2). This implementation advanced the global aerosol forecast capability and made a step forward toward developing a global aerosol data assimilation system. The aerosol products from this system have been used by many applications such as for regional air quality model lateral boundary conditions, satellite sea surface temperature (SST) physical retrievals, and the global solar insolation estimation. Positive impacts have been seen in these applications.

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Aqueous chemical processing within cloud and fog water is thought to be a key process in the production and transformation of secondary organic aerosol mass, found abundantly and ubiquitously throughout the troposphere. Yet, significant uncertainty remains regarding the organic chemical reactions taking place within clouds and the conditions under which those reactions occur, owing to the wide variety of organic compounds and their evolution under highly variable conditions when cycled through clouds. Continuous observations from a fixed remote site like Whiteface Mountain (WFM) in New York State and other mountaintop sites have been used to unravel complex multi-phase interactions in the past, particularly the conversion of gas-phase emissions of SO2 to sulfuric acid within cloud droplets in the presence of sunlight. These scientific insights led to successful control strategies that reduced aerosol sulfate and cloud water acidity substantially over the following decades. This paper provides an overview of observations obtained during a pilot study that took place at WFM in August 2017 aimed at obtaining a better understanding of Chemical Processing of Organic compounds within Clouds (CPOC). During the CPOC pilot study, aerosol cloud activation efficiency, particle size distribution and chemical composition measurements were obtained below-cloud for comparison to routine observations at WFM including cloud water composition and reactive trace gases. Additional instruments deployed for the CPOC pilot study included a doppler LiDAR, sun photometer and radiosondes, to assist in evaluating the meteorological context for the below-cloud and summit observations.