On the effects of the ocean on atmospheric CFC-11 lifetimes and emissions

© 2021 National Academy of Sciences. All rights reserved. The ocean is a reservoir for CFC-11, a major ozone-depleting chemical. Anthropogenic production of CFC-11 dramatically decreased in the 1990s under the Montreal Protocol, which stipulated a global phase out of production by 2010. However, stu...

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Main Authors: Wang, Peidong, Scott, Jeffery R, Solomon, Susan, Marshall, John, Babbin, Andrew R, Lickley, Megan, Thompson, David WJ, DeVries, Timothy, Liang, Qing, Prinn, Ronald G
Format: Article
Language:English
Published: Proceedings of the National Academy of Sciences 2021
Online Access:https://hdl.handle.net/1721.1/133626
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author Wang, Peidong
Scott, Jeffery R
Solomon, Susan
Marshall, John
Babbin, Andrew R
Lickley, Megan
Thompson, David WJ
DeVries, Timothy
Liang, Qing
Prinn, Ronald G
author_facet Wang, Peidong
Scott, Jeffery R
Solomon, Susan
Marshall, John
Babbin, Andrew R
Lickley, Megan
Thompson, David WJ
DeVries, Timothy
Liang, Qing
Prinn, Ronald G
author_sort Wang, Peidong
collection MIT
description © 2021 National Academy of Sciences. All rights reserved. The ocean is a reservoir for CFC-11, a major ozone-depleting chemical. Anthropogenic production of CFC-11 dramatically decreased in the 1990s under the Montreal Protocol, which stipulated a global phase out of production by 2010. However, studies raise questions about current overall emission levels and indicate unexpected increases of CFC-11 emissions of about 10 Gg · yr−1 after 2013 (based upon measured atmospheric concentrations and an assumed atmospheric lifetime). These findings heighten the need to understand processes that could affect the CFC-11 lifetime, including ocean fluxes. We evaluate how ocean uptake and release through 2300 affects CFC-11 lifetimes, emission estimates, and the long-term return of CFC-11 from the ocean reservoir. We show that ocean uptake yields a shorter total lifetime and larger inferred emission of atmospheric CFC-11 from 1930 to 2075 compared to estimates using only atmospheric processes. Ocean flux changes over time result in small but not completely negligible effects on the calculated unexpected emissions change (decreasing it by 0.4 ± 0.3 Gg · yr−1). Moreover, it is expected that the ocean will eventually become a source of CFC-11, increasing its total lifetime thereafter. Ocean outgassing should produce detectable increases in global atmospheric CFC-11 abundances by the mid-2100s, with emission of around 0.5 Gg · yr−1; this should not be confused with illicit production at that time. An illustrative model projection suggests that climate change is expected to make the ocean a weaker reservoir for CFC-11, advancing the detectable change in the global atmospheric mixing ratio by about 5 yr.
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spelling mit-1721.1/1336262021-10-28T04:49:13Z On the effects of the ocean on atmospheric CFC-11 lifetimes and emissions Wang, Peidong Scott, Jeffery R Solomon, Susan Marshall, John Babbin, Andrew R Lickley, Megan Thompson, David WJ DeVries, Timothy Liang, Qing Prinn, Ronald G © 2021 National Academy of Sciences. All rights reserved. The ocean is a reservoir for CFC-11, a major ozone-depleting chemical. Anthropogenic production of CFC-11 dramatically decreased in the 1990s under the Montreal Protocol, which stipulated a global phase out of production by 2010. However, studies raise questions about current overall emission levels and indicate unexpected increases of CFC-11 emissions of about 10 Gg · yr−1 after 2013 (based upon measured atmospheric concentrations and an assumed atmospheric lifetime). These findings heighten the need to understand processes that could affect the CFC-11 lifetime, including ocean fluxes. We evaluate how ocean uptake and release through 2300 affects CFC-11 lifetimes, emission estimates, and the long-term return of CFC-11 from the ocean reservoir. We show that ocean uptake yields a shorter total lifetime and larger inferred emission of atmospheric CFC-11 from 1930 to 2075 compared to estimates using only atmospheric processes. Ocean flux changes over time result in small but not completely negligible effects on the calculated unexpected emissions change (decreasing it by 0.4 ± 0.3 Gg · yr−1). Moreover, it is expected that the ocean will eventually become a source of CFC-11, increasing its total lifetime thereafter. Ocean outgassing should produce detectable increases in global atmospheric CFC-11 abundances by the mid-2100s, with emission of around 0.5 Gg · yr−1; this should not be confused with illicit production at that time. An illustrative model projection suggests that climate change is expected to make the ocean a weaker reservoir for CFC-11, advancing the detectable change in the global atmospheric mixing ratio by about 5 yr. 2021-10-27T19:53:52Z 2021-10-27T19:53:52Z 2021 2021-09-13T18:14:09Z Article http://purl.org/eprint/type/JournalArticle https://hdl.handle.net/1721.1/133626 en 10.1073/PNAS.2021528118 Proceedings of the National Academy of Sciences of the United States of America Creative Commons Attribution-NonCommercial-NoDerivs License http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Proceedings of the National Academy of Sciences PNAS
spellingShingle Wang, Peidong
Scott, Jeffery R
Solomon, Susan
Marshall, John
Babbin, Andrew R
Lickley, Megan
Thompson, David WJ
DeVries, Timothy
Liang, Qing
Prinn, Ronald G
On the effects of the ocean on atmospheric CFC-11 lifetimes and emissions
title On the effects of the ocean on atmospheric CFC-11 lifetimes and emissions
title_full On the effects of the ocean on atmospheric CFC-11 lifetimes and emissions
title_fullStr On the effects of the ocean on atmospheric CFC-11 lifetimes and emissions
title_full_unstemmed On the effects of the ocean on atmospheric CFC-11 lifetimes and emissions
title_short On the effects of the ocean on atmospheric CFC-11 lifetimes and emissions
title_sort on the effects of the ocean on atmospheric cfc 11 lifetimes and emissions
url https://hdl.handle.net/1721.1/133626
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