ScienceDirect® Home Skip Main Navigation Links
You have guest access to ScienceDirect. Find out more.
 
Home
Browse
My Settings
Alerts
Help
 Quick Search
 Search tips (Opens new window)
    Clear all fields    
Chemosphere
Volume 47, Issue 8, June 2002, Pages 851-861
 
Font Size: Decrease Font Size  Increase Font Size
 Abstract - selected
Article
Purchase PDF (414 K)

 
 
 
Related Articles in ScienceDirect
View More Related Articles
 
View Record in Scopus
 
doi:10.1016/S0045-6535(02)00038-3    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2002 Elsevier Science Ltd. All rights reserved.

Dynamic-chemical coupling of the upper troposphere and lower stratosphere region

V. GreweCorresponding Author Contact Information, E-mail The Corresponding Author, a, b, C. Reithmeiera and D. T. Shindellb

a Institut für Physik der Atmosphäre, Deutsches Zentrum für Luft- und Raumfahrt, e.V. (DLR), Oberpfaffenhofen, 82234 Weßling, Germany b NASA Goddard Institute for Space Studies and Center for Climate Systems Research, Columbia University, 2880 Broadway, New York, NY 10025, USA

Received 13 March 2001; 
revised 14 September 2001; 
accepted 5 November 2001. 
Available online 4 March 2002.

Purchase the full-text article



References and further reading may be available for this article. To view references and further reading you must purchase this article.

Abstract

Importance of this paper: The coupling of transport and chemistry in the tropopause region is determined by highly complex interactive processes. Lifetimes of chemical species and vertical mixing rates change rapidly at the tropopause. These coupled processes are simulated with coupled climate–chemistry models and a trajectory model for aircraft and lightning NOx emissions in the upper troposphere. The simulations show that tropical lightning exerts a large influence on the mid-latitude lowermost stratosphere, where it has the potential to form ozone.

Abstract



The importance of the interaction between chemistry and dynamics in the upper troposphere and lower stratosphere for chemical species like ozone is investigated using two chemistry–climate models and a Lagrangian trajectory model. Air parcels from the upper troposphere, i.e. regions of lightning and aircraft emissions, are able to be transported into the lowermost stratosphere (LMS). Trajectory calculations suggest that the main transport pathway runs via the inter tropical convergence zone, across the tropical tropopause and then to higher latitudes, i.e. into the LMS. NOx from aircraft emissions at mid-latitudes are unlikely to perturb the LMS since they are washed-out while still in the troposphere. In contrast, NOx from tropical lightning has the chance to accumulate in the LMS. Because of the longer residence times of NOx in the LMS, compared to the upper troposphere, this excess NOx from lightning has the potential to form ozone in the LMS, which then is transported back to the troposphere at mid-latitudes. In the models, around 10% of the ozone concentration and 50% of the NOx concentration in the northern hemisphere LMS is produced by lightning NOx. At least 5% of the ozone concentration and 35% the NOx concentration at 150 hPa at mid-latitudes originates from tropical lightning in the climate–chemistry simulations.

Author Keywords: UT/LS coupling; Upper troposphere NOx and ozone; Lightning NOx

Article Outline

1. Introduction
2. Model descriptions
3. Methodology
4. Transport of species emitted in the upper troposphere
5. Impact of lightning NOx emissions on the chemistry
6. Origin of mid-latitude ozone increase
7. Discussion and conclusion
Acknowledgements
Appendix A.  
References
Vitae







Chemosphere
Volume 47, Issue 8, June 2002, Pages 851-861
 
Home
Browse
My Settings
Alerts
Help
Elsevier.com (Opens new window)
About ScienceDirect  |  Contact Us  |  Information for Advertisers  |  Terms & Conditions  |  Privacy Policy
Copyright © 2008 Elsevier B.V. All rights reserved. ScienceDirect® is a registered trademark of Elsevier B.V.