Surface temperatures drive strong seasonality in urban reactive carbon emissions

Urban air quality is affected by diverse volatile organic compounds (VOCs), and prior studies reveal a need to understand their seasonal sources. We combine high-resolution mass spectrometry with eddy covariance to quantify VOC fluxes from an urban/suburban New York site during summer and winter. Emissions are strongly seasonal: During summer, twice as many VOCs undergo surface-atmosphere exchange, and molar and reactivity-based fluxes are 2 to 4× higher than in winter. Temperature-dependent emissions from volatile chemical products (VCPs), vegetation, and residences dominate during summer. Ethanol alone accounts for ∼25% of the total flux. During winter, temperature-dependent emissions are reduced and traffic sources dominate. An updated inventory agrees with summer observations within 40% but overestimates winter fluxes by >2.5×. The winter discrepancy reflects overestimated VCP/cooking emissions and missing temperature-dependent volatilization. Results highlight the need to account for seasonal and temperature-dependent urban emissions to support pollution and mitigation assessment in the context of global change.

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Publication Details

Journal
Science Advances
Published
2026-10-07
DOI
https://doi.org/10.1126/sciadv.aef9622
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
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article

Surface temperatures drive strong seasonality in urban reactive carbon emissions

Dylan B. Millet, Trey Maddaleno, Michael P. Vermeuel, Timothy J. Griffis et al.
Science Advances
Atmospheric chemistry and aerosols
article

Surface temperatures drive strong seasonality in urban reactive carbon emissions

Dylan B. Millet, Trey Maddaleno, Michael P. Vermeuel, Timothy J. Griffis, Jeff Peischl, Delphine K. Farmer, Emily Barnes Franklin, Katelyn L. Rediger, Rose K. Rossell, Róisín Commane
article en

Abstract

Urban air quality is affected by diverse volatile organic compounds (VOCs), and prior studies reveal a need to understand their seasonal sources. We combine high-resolution mass spectrometry with eddy covariance to quantify VOC fluxes from an urban/suburban New York site during summer and winter. Emissions are strongly seasonal: During summer, twice as many VOCs undergo surface-atmosphere exchange, and molar and reactivity-based fluxes are 2 to 4× higher than in winter. Temperature-dependent emissions from volatile chemical products (VCPs), vegetation, and residences dominate during summer. Ethanol alone accounts for ∼25% of the total flux. During winter, temperature-dependent emissions are reduced and traffic sources dominate. An updated inventory agrees with summer observations within 40% but overestimates winter fluxes by >2.5×. The winter discrepancy reflects overestimated VCP/cooking emissions and missing temperature-dependent volatilization. Results highlight the need to account for seasonal and temperature-dependent urban emissions to support pollution and mitigation assessment in the context of global change.

Science AdvancesVol. 12(41)
University of Minnesota (US), National Oceanic and Atmospheric Administration (US), Cooperative Institute for Research in Environmental Sciences (US), University of Colorado Boulder (US), Purdue University West Lafayette (US), Health Sciences and Nutrition (AU), NOAA Global Monitoring Laboratory, Columbia University (US), Colorado State University (US)
Openalex Percentile: Top 19%
Atmospheric chemistry and aerosols
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