Isotopic source signatures of stratospheric CO inferred from in situ vertical profiles

The stratospheric CO budget is determined by CH<sub>4</sub> oxidation, OH-driven loss and atmospheric transport. These processes can be constrained using CO mole fractions and isotopic compositions, with the latter being largely unexplored. We present novel stratospheric observations of δ<sup>13</sup>C-CO and δ<sup>18</sup>O-CO vertical profiles, revealing distinct altitude-dependent trends. δ<sup>13</sup>C-CO decreases with altitude due to inverse <sup>13</sup>C kinetic fractionation in the OH sink and <sup>13</sup>C-depleted CO from CH<sub>4</sub> oxidation. In contrast, δ<sup>18</sup>O-CO increases with altitude, driven by <sup>18</sup>O-rich oxygen from O(<sup>1</sup>D) via O<sub>3</sub> photolysis and CO<sub>2</sub> photolysis. Our findings suggest that CO isotopes can act as valuable proxies for quantifying CO production from CO<sub>2</sub> photolysis. Incorporating CO mole fractions and isotopic data into global models enhances evaluations of the stratospheric CH<sub>4</sub> sink and OH abundance, improving our understanding of stratospheric water vapour and its radiative impacts.

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Journal
npj Climate and Atmospheric Science
Published
2025-03-18
DOI
https://doi.org/10.1038/s41612-025-00986-1
Primary Topic
Atmospheric and Environmental Gas Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Isotopic source signatures of stratospheric CO inferred from in situ vertical profiles

Sergey Gromov, Huilin Chen, María Elena Popa, Joram Hooghiem et al.
npj Climate and Atmospheric Science
Atmospheric and Environmental Gas Dynamics
article

Isotopic source signatures of stratospheric CO inferred from in situ vertical profiles

Sergey Gromov, Huilin Chen, María Elena Popa, Joram Hooghiem, Rigel Kivi, Thomas Röckmann
article en

Abstract

The stratospheric CO budget is determined by CH<sub>4</sub> oxidation, OH-driven loss and atmospheric transport. These processes can be constrained using CO mole fractions and isotopic compositions, with the latter being largely unexplored. We present novel stratospheric observations of δ<sup>13</sup>C-CO and δ<sup>18</sup>O-CO vertical profiles, revealing distinct altitude-dependent trends. δ<sup>13</sup>C-CO decreases with altitude due to inverse <sup>13</sup>C kinetic fractionation in the OH sink and <sup>13</sup>C-depleted CO from CH<sub>4</sub> oxidation. In contrast, δ<sup>18</sup>O-CO increases with altitude, driven by <sup>18</sup>O-rich oxygen from O(<sup>1</sup>D) via O<sub>3</sub> photolysis and CO<sub>2</sub> photolysis. Our findings suggest that CO isotopes can act as valuable proxies for quantifying CO production from CO<sub>2</sub> photolysis. Incorporating CO mole fractions and isotopic data into global models enhances evaluations of the stratospheric CH<sub>4</sub> sink and OH abundance, improving our understanding of stratospheric water vapour and its radiative impacts.

npj Climate and Atmospheric ScienceVol. 8(1)
Finnish Meteorological Institute (FI), University of Groningen (NL), Utrecht University (NL), Max Planck Institute for Chemistry (DE), Nanjing University (CN), Wageningen University & Research (NL)
National Natural Science Foundation of China, Chinese Academy of Sciences, Netherlands Space Office, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, National Key Research and Development Program of China
Openalex Percentile: Top 94%
Atmospheric and Environmental Gas Dynamics
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