Surface Anthropogenic NO <sub>x</sub> Emissions Drive 1995–2014 Increase in Tropospheric Ozone: Implications for Ozone and Methane Radiative Forcing

Abstract Tropospheric ozone influences Earth's radiative energy budget and has increased in recent decades. With initial‐condition ensembles from a single chemistry‐climate model, we show that global surface anthropogenic NO x emissions explain about 90% of the simulated 1995–2014 tropospheric ozone increase (1.8 DU) and that this increase exceeds those arising internally from natural climate variability. South and East Asian NO x emissions account for about 40% of the global NO x ‐driven ozone increase but contribute about 80% of the associated net positive stratospheric‐adjusted radiative forcing (SARF; tropospheric ozone plus methane), reflecting a weaker methane response to Asian NO x than to tropical surface NO x emissions. Considering both CO + NMVOC and NO x emissions from Asia produces a larger net SARF than from global emissions (+0.032 vs. +0.023 W m −2 ). Tropospheric ozone changes over 1995–2014 from global CO + NMVOC emissions or methane concentrations alone are too small to be detected relative to internal climate variability.

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Journal
Geophysical Research Letters
Published
2026-06-18
DOI
https://doi.org/10.1029/2025gl121529
Primary Topic
Atmospheric chemistry and aerosols
Type
article
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article

Surface Anthropogenic NO x Emissions Drive 1995–2014 Increase in Tropospheric Ozone: Implications for Ozone and Methane Radiative Forcing

Arlene M. Fiore, Ragnhild Bieltvedt Skeie, Jeffery R. Scott, Sebastian D. Eastham et al.
Geophysical Research Letters
Atmospheric chemistry and aerosols
article

Surface Anthropogenic NO x Emissions Drive 1995–2014 Increase in Tropospheric Ozone: Implications for Ozone and Methane Radiative Forcing

Arlene M. Fiore, Ragnhild Bieltvedt Skeie, Jeffery R. Scott, Sebastian D. Eastham, Stephanie Elkins, Xinyuan Yu, Jean‐François Lamarque
article en

Abstract

Abstract Tropospheric ozone influences Earth's radiative energy budget and has increased in recent decades. With initial‐condition ensembles from a single chemistry‐climate model, we show that global surface anthropogenic NO x emissions explain about 90% of the simulated 1995–2014 tropospheric ozone increase (1.8 DU) and that this increase exceeds those arising internally from natural climate variability. South and East Asian NO x emissions account for about 40% of the global NO x ‐driven ozone increase but contribute about 80% of the associated net positive stratospheric‐adjusted radiative forcing (SARF; tropospheric ozone plus methane), reflecting a weaker methane response to Asian NO x than to tropical surface NO x emissions. Considering both CO + NMVOC and NO x emissions from Asia produces a larger net SARF than from global emissions (+0.032 vs. +0.023 W m −2 ). Tropospheric ozone changes over 1995–2014 from global CO + NMVOC emissions or methane concentrations alone are too small to be detected relative to internal climate variability.

Geophysical Research LettersVol. 53(12)
NSF National Center for Atmospheric Research (US), Cicatelli Associates (US), CICERO Center for International Climate Research (NO), Imperial College London (GB), Massachusetts Institute of Technology (US)
Climate action
Openalex Percentile: Top 6%
Atmospheric chemistry and aerosols
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