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Kenneth R. Knapp, Steve Ansari, Caroline L. Bain, Mark A. Bourassa, Michael J. Dickinson, Chris Funk, Chip N. Helms, Christopher C. Hennon, Christopher D. Holmes, George J. Huffman, James P. Kossin, Hai-Tien Lee, Alexander Loew, and Gudrun Magnusdottir

Geostationary satellites have provided routine, high temporal resolution Earth observations since the 1970s. Despite the long period of record, use of these data in climate studies has been limited for numerous reasons, among them that no central archive of geostationary data for all international satellites exists, full temporal and spatial resolution data are voluminous, and diverse calibration and navigation formats encumber the uniform processing needed for multisatellite climate studies. The International Satellite Cloud Climatology Project (ISCCP) set the stage for overcoming these issues by archiving a subset of the full-resolution geostationary data at ~10-km resolution at 3-hourly intervals since 1983. Recent efforts at NOAA's National Climatic Data Center to provide convenient access to these data include remapping the data to a standard map projection, recalibrating the data to optimize temporal homogeneity, extending the record of observations back to 1980, and reformatting the data for broad public distribution. The Gridded Satellite (GridSat) dataset includes observations from the visible, infrared window, and infrared water vapor channels. Data are stored in Network Common Data Format (netCDF) using standards that permit a wide variety of tools and libraries to process the data quickly and easily. A novel data layering approach, together with appropriate satellite and file metadata, allows users to access GridSat data at varying levels of complexity based on their needs. The result is a climate data record already in use by the meteorological community. Examples include reanalysis of tropical cyclones, studies of global precipitation, and detection and tracking of the intertropical convergence zone.

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A. Gannet Hallar, Steven S. Brown, Erik Crosman, Kelley C. Barsanti, Christopher D. Cappa, Ian Faloona, Jerome Fast, Heather A. Holmes, John Horel, John Lin, Ann Middlebrook, Logan Mitchell, Jennifer Murphy, Caroline C. Womack, Viney Aneja, Munkhbayar Baasandorj, Roya Bahreini, Robert Banta, Casey Bray, Alan Brewer, Dana Caulton, Joost de Gouw, Stephan F.J. De Wekker, Delphine K. Farmer, Cassandra J. Gaston, Sebastian Hoch, Francesca Hopkins, Nakul N. Karle, James T. Kelly, Kerry Kelly, Neil Lareau, Keding Lu, Roy L. Mauldin III, Derek V. Mallia, Randal Martin, Daniel L. Mendoza, Holly J. Oldroyd, Yelena Pichugina, Kerri A. Pratt, Pablo E. Saide, Philip J. Silva, William Simpson, Britton B. Stephens, Jochen Stutz, and Amy Sullivan


Wintertime episodes of high aerosol concentrations occur frequently in urban and agricultural basins and valleys worldwide. These episodes often arise following development of persistent cold-air pools (PCAPs) that limit mixing and modify chemistry. While field campaigns targeting either basin meteorology or wintertime pollution chemistry have been conducted, coupling between interconnected chemical and meteorological processes remains an insufficiently studied research area. Gaps in understanding the coupled chemical–meteorological interactions that drive high-pollution events make identification of the most effective air-basin specific emission control strategies challenging. To address this, a September 2019 workshop occurred with the goal of planning a future research campaign to investigate air quality in western U.S. basins. Approximately 120 people participated, representing 50 institutions and five countries. Workshop participants outlined the rationale and design for a comprehensive wintertime study that would couple atmospheric chemistry and boundary layer and complex-terrain meteorology within western U.S. basins. Participants concluded the study should focus on two regions with contrasting aerosol chemistry: three populated valleys within Utah (Salt Lake, Utah, and Cache Valleys) and the San Joaquin Valley in California. This paper describes the scientific rationale for a campaign that will acquire chemical and meteorological datasets using airborne platforms with extensive range, coupled to surface-based measurements focusing on sampling within the near-surface boundary layer, and transport and mixing processes within this layer, with high vertical resolution at a number of representative sites. No prior wintertime basin-focused campaign has provided the breadth of observations necessary to characterize the meteorological–chemical linkages outlined here, nor to validate complex processes within coupled atmosphere–chemistry models.

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