Tropospheric ozone and aerosols measured by airborne lidar during the 1988 Arctic boundary layer experiment

Ozone (O3) and aerosol distributions were measured from an aircraft using a differential absorption lidar (DIAL) system as part of the 1988 NASA Global Tropospheric Experiment - Arctic Boundary Layer Experiment (ABLE-3A) to study the sources and sinks of gases and aerosols over the tundra regions of...

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Main Authors: Butler, Carolyn F., Kooi, Susan A., Browell, Edward V.
Format: Other/Unknown Material
Language:unknown
Published: 1991
Subjects:
Online Access:http://hdl.handle.net/2060/19910016141
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spelling ftnasantrs:oai:casi.ntrs.nasa.gov:19910016141 2023-05-15T14:51:07+02:00 Tropospheric ozone and aerosols measured by airborne lidar during the 1988 Arctic boundary layer experiment Butler, Carolyn F. Kooi, Susan A. Browell, Edward V. Unclassified, Unlimited, Publicly available JAN 1, 1991 application/pdf http://hdl.handle.net/2060/19910016141 unknown Document ID: 19910016141 Accession ID: 91N25455 http://hdl.handle.net/2060/19910016141 No Copyright CASI ENVIRONMENT POLLUTION NASA, Washington, 4th Airborne Geoscience Workshop; p 119-120 1991 ftnasantrs 2015-03-15T05:17:19Z Ozone (O3) and aerosol distributions were measured from an aircraft using a differential absorption lidar (DIAL) system as part of the 1988 NASA Global Tropospheric Experiment - Arctic Boundary Layer Experiment (ABLE-3A) to study the sources and sinks of gases and aerosols over the tundra regions of Alaska during the summer. The tropospheric O3 budget over the Arctic was found to be strongly influenced by stratospheric intrusions. Regions of low aerosol scattering and enhanced O3 mixing ratios were usually correlated with descending air from the upper troposphere or lower stratosphere. Several cases of continental polar air masses were examined during the experiment. The aerosol scattering associated with these air masses was very low, and the atmospheric distribution of aerosols was quite homogeneous for those air masses that had been transported over the ice for greater than or = 3 days. The transition in O3 and aerosol distributions from tundra to marine conditions was examined several times. The aerosol data clearly show an abrupt change in aerosol scattering properties within the mixed layer from lower values over the tundra to generally higher values over the water. The distinct differences in the heights of the mixed layers in the two regions was also readily apparent. Several cases of enhanced O3 were observed during ABLE-3 in conjunction with enhanced aerosol scattering in layers in the free atmosphere. Examples are presented of the large scale variations of O3 and aerosols observed with the airborne lidar system from near the surface to above the tropopause over the Arctic during ABLE-3. Other/Unknown Material Arctic Tundra Alaska NASA Technical Reports Server (NTRS) Arctic
institution Open Polar
collection NASA Technical Reports Server (NTRS)
op_collection_id ftnasantrs
language unknown
topic ENVIRONMENT POLLUTION
spellingShingle ENVIRONMENT POLLUTION
Butler, Carolyn F.
Kooi, Susan A.
Browell, Edward V.
Tropospheric ozone and aerosols measured by airborne lidar during the 1988 Arctic boundary layer experiment
topic_facet ENVIRONMENT POLLUTION
description Ozone (O3) and aerosol distributions were measured from an aircraft using a differential absorption lidar (DIAL) system as part of the 1988 NASA Global Tropospheric Experiment - Arctic Boundary Layer Experiment (ABLE-3A) to study the sources and sinks of gases and aerosols over the tundra regions of Alaska during the summer. The tropospheric O3 budget over the Arctic was found to be strongly influenced by stratospheric intrusions. Regions of low aerosol scattering and enhanced O3 mixing ratios were usually correlated with descending air from the upper troposphere or lower stratosphere. Several cases of continental polar air masses were examined during the experiment. The aerosol scattering associated with these air masses was very low, and the atmospheric distribution of aerosols was quite homogeneous for those air masses that had been transported over the ice for greater than or = 3 days. The transition in O3 and aerosol distributions from tundra to marine conditions was examined several times. The aerosol data clearly show an abrupt change in aerosol scattering properties within the mixed layer from lower values over the tundra to generally higher values over the water. The distinct differences in the heights of the mixed layers in the two regions was also readily apparent. Several cases of enhanced O3 were observed during ABLE-3 in conjunction with enhanced aerosol scattering in layers in the free atmosphere. Examples are presented of the large scale variations of O3 and aerosols observed with the airborne lidar system from near the surface to above the tropopause over the Arctic during ABLE-3.
format Other/Unknown Material
author Butler, Carolyn F.
Kooi, Susan A.
Browell, Edward V.
author_facet Butler, Carolyn F.
Kooi, Susan A.
Browell, Edward V.
author_sort Butler, Carolyn F.
title Tropospheric ozone and aerosols measured by airborne lidar during the 1988 Arctic boundary layer experiment
title_short Tropospheric ozone and aerosols measured by airborne lidar during the 1988 Arctic boundary layer experiment
title_full Tropospheric ozone and aerosols measured by airborne lidar during the 1988 Arctic boundary layer experiment
title_fullStr Tropospheric ozone and aerosols measured by airborne lidar during the 1988 Arctic boundary layer experiment
title_full_unstemmed Tropospheric ozone and aerosols measured by airborne lidar during the 1988 Arctic boundary layer experiment
title_sort tropospheric ozone and aerosols measured by airborne lidar during the 1988 arctic boundary layer experiment
publishDate 1991
url http://hdl.handle.net/2060/19910016141
op_coverage Unclassified, Unlimited, Publicly available
geographic Arctic
geographic_facet Arctic
genre Arctic
Tundra
Alaska
genre_facet Arctic
Tundra
Alaska
op_source CASI
op_relation Document ID: 19910016141
Accession ID: 91N25455
http://hdl.handle.net/2060/19910016141
op_rights No Copyright
_version_ 1766322188631146496