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Full-Text Articles in Physical Sciences and Mathematics
Sources And Chemistry Of Noₓ In The Upper Troposphere Over The United States, Lyatt Jaegle, Daniel J. Jacob, Yuhua Wang, Andrew J. Weinheimer, Brian A. Ridley, Teresa L. Campos, Glen W. Sachse, Donald E. Hagen
Sources And Chemistry Of Noₓ In The Upper Troposphere Over The United States, Lyatt Jaegle, Daniel J. Jacob, Yuhua Wang, Andrew J. Weinheimer, Brian A. Ridley, Teresa L. Campos, Glen W. Sachse, Donald E. Hagen
Physics Faculty Research & Creative Works
The origin of NOx in the upper troposphere over the central United States is examined using aircraft observations obtained during the SUCCESS campaign in April–May of 1996. Correlations between NOy (sum of NOx and its oxidation products) and CO at 8–12 km altitude indicate that NOx originates primarily from convective transport of polluted boundary layer air. Lightning and aircraft emissions appear to be only minor sources of NOx. Chemical steady state model calculations constrained by local observations of NO underestimate the measured NOx/NOy concentration ratio at 8–12 km altitude by a …
Observation Of Upper Tropospheric Sulfur Dioxide- And Acetone-Pollution: Potential Implications For Hydroxyl Radical And Aerosol Formation, F. Arnold, J. Schneider, K. Gollinger, H. Schlager, P. Schulte, Donald E. Hagen, Philip D. Whitefield, Peter F. J. Van Velthoven
Observation Of Upper Tropospheric Sulfur Dioxide- And Acetone-Pollution: Potential Implications For Hydroxyl Radical And Aerosol Formation, F. Arnold, J. Schneider, K. Gollinger, H. Schlager, P. Schulte, Donald E. Hagen, Philip D. Whitefield, Peter F. J. Van Velthoven
Physics Faculty Research & Creative Works
Aircraft-based measurements of sulfur dioxide, acetone, carbon dioxide, and condensation nuclei (CN) were made over the north-eastern Atlantic at upper tropospheric altitudes, around 9000 m. On October 14, 1993, strong SO 2- and acetone-pollution (both up to 3 ppbv) were observed, which were accompanied by a CO 2-enhancement of up to 6 ppmv, and large CN-concentrations of up to about 1500 cm -3 (for radii ≥ 6 nm). CN, excess CO 2, and to a lesser degree also acetone, were positively correlated with SO 2. Air mass trajectory analyses indicate, that most of the air masses …
Upper-Tropospheric Aerosol Sampled During Project Fire Ifo Ii, Donald E. Hagen, Josef Podzimek, Max B. Trueblood
Upper-Tropospheric Aerosol Sampled During Project Fire Ifo Ii, Donald E. Hagen, Josef Podzimek, Max B. Trueblood
Physics Faculty Research & Creative Works
Aerosols can play a role in the cloud formation process through the heterogeneous nucleation mechanism, and in turn, once formed, cirrus clouds can impact the ambient aerosol through scavenging and other collection mechanisms. University of Missouri aerosol sampling facilities were employed on aircraft for in situ collection and characterization of the particulates near cirrus cloud level. Tandem differential mobility analyzer and impactor techniques were used to measure aerosol size distribution, hydration capability, and particle composition information. Evidence of aerosol layering was observed near the tropospause, and there was a tendency toward depletion of the ambient aerosol at both ends of …