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dc.contributor.author
Li, Qinyi  
dc.contributor.author
Meidan, Daphne  
dc.contributor.author
Hess, Peter Otto  
dc.contributor.author
Añel, Juan A.  
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Cuevas, Carlos Alberto  
dc.contributor.author
Doney, Scott  
dc.contributor.author
Fernandez, Rafael Pedro  
dc.contributor.author
van Herpen, Maarten  
dc.contributor.author
Höglund Isaksson, Lena  
dc.contributor.author
Johnson, Matthew S.  
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Kinnison, Douglas E.  
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Lamarque, Jean Francoise  
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Röckmann, Thomas  
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Mahowald, Natalie M.  
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Saiz López, Alfonso  
dc.date.available
2024-10-10T15:49:08Z  
dc.date.issued
2023-07-08  
dc.identifier.citation
Li, Qinyi; Meidan, Daphne; Hess, Peter Otto; Añel, Juan A.; Cuevas, Carlos Alberto; et al.; Global environmental implications of atmospheric methane removal through chlorine-mediated chemistry-climate interactions; Nature; Nature Communications; 14; 1; 8-7-2023; 1 - 10  
dc.identifier.uri
http://hdl.handle.net/11336/245904  
dc.description.abstract
Atmospheric methane is both a potent greenhouse gas and photochemically active, with approximately equal anthropogenic and natural sources. The addition of chlorine to the atmosphere has been proposed to mitigate global warming through methane reduction by increasing its chemical loss. However, the potential environmental impacts of such climate mitigation remainunexplored. Here, sensitivity studies are conducted to evaluate the possible effects of increasing reactive chlorine emissions on the methane budget, atmospheric composition and radiative forcing. Because of non-linear chemistry, in order to achieve a reduction in methane burden (instead of anincrease), the chlorine atom burden needs to be a minimum of three times the estimated present-day burden. If the methane removal target is set to 20%, 45%, or 70% less global methane by 2050 compared to the levels in the Representative Concentration Pathway 8.5 scenario (RCP8.5), our modeling results suggest that additional chlorine fluxes of 630, 1250, and 1880 Tg Cl/year, respectively, are needed. The results show that increasing chlorine emissions also induces significant changes in other important climate forcers. Remarkably, the tropospheric ozone decrease is large enough that the magnitude of radiative forcing decrease is similar to that of methane. Adding 630, 1250, and 1880 Tg Cl/year to the RCP8.5 scenario, chosen to have the mostconsistent current-day trends of methane, will decrease the surface temperature by 0.2, 0.4, and 0.6 °C by 2050, respectively. The quantity and method in which the chlorine is added, its interactions with climate pathways, and the potential environmental impacts on air quality and ocean acidity, must be carefully considered before any action is taken.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Nature  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/  
dc.subject
Methane removal  
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Chlorine-driven loss  
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Cl2 Source  
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Ciencias Medioambientales  
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Ciencias de la Tierra y relacionadas con el Medio Ambiente  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Global environmental implications of atmospheric methane removal through chlorine-mediated chemistry-climate interactions  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2024-08-26T10:57:43Z  
dc.identifier.eissn
2041-1723  
dc.journal.volume
14  
dc.journal.number
1  
dc.journal.pagination
1 - 10  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Li, Qinyi. Consejo Superior de Investigaciones Cientícas. Instituto de Quimica Física Blas Cabrera; España. Consejo Superior de Investigaciones Científicas; España. Universidad Politécnica de Hong Kong; China. Shandong University; China. Universidad de Shandong. Instituto de Investigación Ambiental; China  
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Fil: Meidan, Daphne. Cornell University; Estados Unidos  
dc.description.fil
Fil: Hess, Peter Otto. Cornell University; Estados Unidos  
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Fil: Añel, Juan A.. Consejo Superior de Investigaciones Cientícas. Instituto de Quimica Física Blas Cabrera; España. Universidad de Vigo; España  
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Fil: Cuevas, Carlos Alberto. Consejo Superior de Investigaciones Cientícas. Instituto de Quimica Física Blas Cabrera; España. Consejo Superior de Investigaciones Científicas; España  
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Fil: Doney, Scott. University of Virginia; Estados Unidos  
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Fil: Fernandez, Rafael Pedro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto Interdisciplinario de Ciencias Básicas. - Universidad Nacional de Cuyo. Instituto Interdisciplinario de Ciencias Básicas; Argentina  
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Fil: van Herpen, Maarten. No especifíca;  
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Fil: Höglund Isaksson, Lena. No especifíca;  
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Fil: Johnson, Matthew S.. Universidad de Copenhagen; Dinamarca  
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Fil: Kinnison, Douglas E.. National Center for Atmospheric Research; Estados Unidos  
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Fil: Lamarque, Jean Francoise. National Center for Atmospheric Research; Estados Unidos  
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Fil: Röckmann, Thomas. University of Utrecht; Países Bajos  
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Fil: Mahowald, Natalie M.. Cornell University; Estados Unidos  
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Fil: Saiz López, Alfonso. Consejo Superior de Investigaciones Cientícas. Instituto de Quimica Física Blas Cabrera; España  
dc.journal.title
Nature Communications  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1038/s41467-023-39794-7  
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info:eu-repo/semantics/altIdentifier/url/https://www.nature.com/articles/s41467-023-39794-7  
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info:eu-repo/semantics/altIdentifier/url/https://pubmed.ncbi.nlm.nih.gov/37422475/