- A41G-07: Stratospheric in Situ Measurements of N2O5 Constrain and Parameterize Heterogeneous Chemistry and Its Influence on Ozone
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Zachary Decker, Cooperative Institute for Research in Environmental Sciences, CU Boulder (First Author, Presenting Author)
Gordon Novak, NOAA Chemical Sciences Laboratory
Ewa Bednarz, CIRES / NOAA Chemical Sciences Laboratory
Steven Brown, NOAA Chemical Sciences Laboratory
Adam Ahern, NOAA
Thaopaul Bui, NASA Ames Research Center
Jonathan Dean-Day, Bay Area Environmental Research Institute
Glenn Diskin, NASA Langley Research Center
Geoffrey Dutton, Cooperative Institute for Research in Environmental Sciences
Colin Gurganus, Cooperative Institute for Research in Environmental Sciences
Brad Hall, Retired
Eric Hintsa, Cooperative Institute for Research in Environmental Sciences
Christopher Jernigan, Environmental Protection Agency
Michael Lawler, Cooperative Institute for Research in Environmental Sciences
Ming Lyu, Cooperative Institute for Research in Environmental Sciences
Samantha Lee, Cooperative Institute for Research in Environmental Sciences (CIRES)
Fred Moore, Cooperative Institute for Research in Environmental Sciences
Daniel Murphy, NOAA Chemical Sciences Laboratory
Jon Nance, Cooperative Institute for Research in Environmental Sciences
Eric Ray, Cooperative Institute for Research in Environmental Sciences
Michael Robinson, Cooperative Institute for Research in Environmental Sciences
Gregory Schill, NOAA Chemical Sciences Laboratory
Troy Thornberry, NOAA Chemical Sciences Laboratory
Patrick Veres, National Center for Atmospheric Research
Eleanor Waxman, Cooperative Institute for Research in Environmental Sciences
Andrew Rollins, NOAA Chemical Sciences Laboratory
The stratospheric ozone layer is critical to our planet and the health of the planet's population. The chemical reactions influencing ozone in the stratosphere are difficult to study because the stratosphere is difficult to reach. Our work presents new in situ observations of dinitrogen pentoxide (N2O5), a critical molecule that influences stratospheric ozone. These first-time observations stem from the NOAA Stratospheric Aerosol Processes, Budget, and Radiative Effects (SABRE) campaign. In combination with simultaneous observations, new data on N2O5 greatly improve our understanding of key gas/particle reactions that alter ozone. Our results show striking variability in the reaction rate — previously considered to be a constant value. The rate varies by factors of up to 100x. The results show that different stratospheric particles exhibit different reaction rates, depending on where the particle originated (for example, volcanic, mesospheric, wildfire, etc.). Further, the rate is strongly correlated with common stratospheric tracer molecules, such as N2O, allowing for new methods of inputting the reaction rate into current global models of ozone. In doing so, our results suggest modeled ozone changes on the scale of single percent — comparable to the scale of observed decadal-time-scale changes in stratospheric O3.
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