Winter- and summertime continental influences on tropospheric O3 and CO observed by TES over the western North Atlantic Ocean

The distributions of tropospheric ozone (O 3 ) and carbon monoxide (CO), and the synoptic factors regulating these distributions over the western North Atlantic Ocean during winter and summer were investigated using profile retrievals from the Tropospheric Emission Spectrometer (TES) for 2004–2006....

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Published in:Atmospheric Chemistry and Physics
Main Authors: Hegarty, J., Mao, H., Talbot, R.
Format: Text
Language:English
Published: 2018
Subjects:
Online Access:https://doi.org/10.5194/acp-10-3723-2010
https://www.atmos-chem-phys.net/10/3723/2010/
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spelling ftcopernicus:oai:publications.copernicus.org:acp1885 2023-05-15T17:31:16+02:00 Winter- and summertime continental influences on tropospheric O3 and CO observed by TES over the western North Atlantic Ocean Hegarty, J. Mao, H. Talbot, R. 2018-01-15 application/pdf https://doi.org/10.5194/acp-10-3723-2010 https://www.atmos-chem-phys.net/10/3723/2010/ eng eng doi:10.5194/acp-10-3723-2010 https://www.atmos-chem-phys.net/10/3723/2010/ eISSN: 1680-7324 Text 2018 ftcopernicus https://doi.org/10.5194/acp-10-3723-2010 2019-12-24T09:57:25Z The distributions of tropospheric ozone (O 3 ) and carbon monoxide (CO), and the synoptic factors regulating these distributions over the western North Atlantic Ocean during winter and summer were investigated using profile retrievals from the Tropospheric Emission Spectrometer (TES) for 2004–2006. Seasonal composites of TES retrievals, reprocessed to remove the influence of the a priori on geographical and seasonal structure, exhibited strong seasonal differences. At the 681 hPa level during winter months of December, January and February (DJF) the composite O 3 mixing ratios were uniformly low (~45 ppbv), but continental export was evident in a channel of enhanced CO (100–110 ppbv) flowing eastward from the US coast. In summer months June, July, and August (JJA) O 3 mixing ratios were variable (45–65 ppbv) and generally higher due to increased photochemical production. The summer distribution also featured a channel of enhanced CO (95–105 ppbv) flowing northeastward around an anticyclone and exiting the continent over the Canadian Maritimes around 50° N. Offshore O 3 -CO slopes were generally 0.15–0.20 mol mol −1 in JJA, indicative of photochemical O 3 production. Composites for 4 predominant synoptic patterns or map types in DJF suggested that export to the lower free troposphere (681 hPa level) was enhanced by the warm conveyor belt airstream of mid-latitude cyclones while stratospheric intrusions increased TES O 3 levels at 316 hPa. A major finding in the DJF data was that offshore 681 hPa CO mixing ratios behind cold fronts could be enhanced up to >150 ppbv likely by lofting from the surface via shallow convection resulting from rapid destabilization of cold air flowing over much warmer ocean waters. In JJA composites for 3 map types showed that the general export pattern of the seasonal composites was associated with a synoptic pattern featuring the Bermuda High. However, weak cyclones and frontal troughs could enhance offshore 681 hPa CO mixing ratios to >110 ppbv with O 3 -CO slopes >0.50 mol mol −1 south of 45° N. Intense cyclones, which were not as common in the summer, enhanced export by lofting of boundary layer pollutants from over the US and also provided a possible mechanism for transporting pollutants from boreal fire outflow southward to the US east coast. Overall, for winter and summer the TES retrievals showed substantial evidence of air pollution export to the western North Atlantic Ocean with the most distinct differences in distribution patterns related to strong influences of mid-latitude cyclones in winter and the Bermuda High anticyclone in summer. Text North Atlantic Copernicus Publications: E-Journals Atmospheric Chemistry and Physics 10 8 3723 3741
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language English
description The distributions of tropospheric ozone (O 3 ) and carbon monoxide (CO), and the synoptic factors regulating these distributions over the western North Atlantic Ocean during winter and summer were investigated using profile retrievals from the Tropospheric Emission Spectrometer (TES) for 2004–2006. Seasonal composites of TES retrievals, reprocessed to remove the influence of the a priori on geographical and seasonal structure, exhibited strong seasonal differences. At the 681 hPa level during winter months of December, January and February (DJF) the composite O 3 mixing ratios were uniformly low (~45 ppbv), but continental export was evident in a channel of enhanced CO (100–110 ppbv) flowing eastward from the US coast. In summer months June, July, and August (JJA) O 3 mixing ratios were variable (45–65 ppbv) and generally higher due to increased photochemical production. The summer distribution also featured a channel of enhanced CO (95–105 ppbv) flowing northeastward around an anticyclone and exiting the continent over the Canadian Maritimes around 50° N. Offshore O 3 -CO slopes were generally 0.15–0.20 mol mol −1 in JJA, indicative of photochemical O 3 production. Composites for 4 predominant synoptic patterns or map types in DJF suggested that export to the lower free troposphere (681 hPa level) was enhanced by the warm conveyor belt airstream of mid-latitude cyclones while stratospheric intrusions increased TES O 3 levels at 316 hPa. A major finding in the DJF data was that offshore 681 hPa CO mixing ratios behind cold fronts could be enhanced up to >150 ppbv likely by lofting from the surface via shallow convection resulting from rapid destabilization of cold air flowing over much warmer ocean waters. In JJA composites for 3 map types showed that the general export pattern of the seasonal composites was associated with a synoptic pattern featuring the Bermuda High. However, weak cyclones and frontal troughs could enhance offshore 681 hPa CO mixing ratios to >110 ppbv with O 3 -CO slopes >0.50 mol mol −1 south of 45° N. Intense cyclones, which were not as common in the summer, enhanced export by lofting of boundary layer pollutants from over the US and also provided a possible mechanism for transporting pollutants from boreal fire outflow southward to the US east coast. Overall, for winter and summer the TES retrievals showed substantial evidence of air pollution export to the western North Atlantic Ocean with the most distinct differences in distribution patterns related to strong influences of mid-latitude cyclones in winter and the Bermuda High anticyclone in summer.
format Text
author Hegarty, J.
Mao, H.
Talbot, R.
spellingShingle Hegarty, J.
Mao, H.
Talbot, R.
Winter- and summertime continental influences on tropospheric O3 and CO observed by TES over the western North Atlantic Ocean
author_facet Hegarty, J.
Mao, H.
Talbot, R.
author_sort Hegarty, J.
title Winter- and summertime continental influences on tropospheric O3 and CO observed by TES over the western North Atlantic Ocean
title_short Winter- and summertime continental influences on tropospheric O3 and CO observed by TES over the western North Atlantic Ocean
title_full Winter- and summertime continental influences on tropospheric O3 and CO observed by TES over the western North Atlantic Ocean
title_fullStr Winter- and summertime continental influences on tropospheric O3 and CO observed by TES over the western North Atlantic Ocean
title_full_unstemmed Winter- and summertime continental influences on tropospheric O3 and CO observed by TES over the western North Atlantic Ocean
title_sort winter- and summertime continental influences on tropospheric o3 and co observed by tes over the western north atlantic ocean
publishDate 2018
url https://doi.org/10.5194/acp-10-3723-2010
https://www.atmos-chem-phys.net/10/3723/2010/
genre North Atlantic
genre_facet North Atlantic
op_source eISSN: 1680-7324
op_relation doi:10.5194/acp-10-3723-2010
https://www.atmos-chem-phys.net/10/3723/2010/
op_doi https://doi.org/10.5194/acp-10-3723-2010
container_title Atmospheric Chemistry and Physics
container_volume 10
container_issue 8
container_start_page 3723
op_container_end_page 3741
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