Measurement report: Extreme heat and wildfire emissions enhance volatile organic compounds in a temperate forest

Abstract. Climate extremes are projected to cause unprecedented deviations in the emission and transformation of volatile organic compounds (VOCs), which trigger feedback mechanisms that will impact the atmospheric oxidation and formation of aerosols and clouds. However, the response of VOCs to future conditions such as extreme heat and wildfire events is still uncertain. This study explored the modification of the mixing ratio and distribution of several anthropogenic and biogenic VOCs in a temperate oak–hickory–juniper forest as a response to increased temperature and transported biomass burning plumes. A chemical ionization mass spectrometer was deployed on a tower at a height of 32 m in rural central Missouri, United States, for the continuous and in situ measurement of VOCs from June to August of 2023. The maximum observed temperature in the region was 38 °C, and during multiple episodes the temperature remained above 32 °C for several hours. Biogenic VOCs such as isoprene and monoterpene followed closely the temperature daily profile but at varying rates, whereas anthropogenic VOCs were insensitive to elevated temperature. During the measurement period, wildfire emissions were transported to the site and substantially increased the mixing ratios of acetonitrile and benzene, which are produced from burning of biomass. An in-depth analysis of the mass spectra revealed more than 250 minor compounds, such as formamide and methylglyoxal. Extreme heat and presence of wildfire plumes modified the overall volatility, reactivity, O : C, and H : C ratios of the extended list of VOCs. The calculated OH reactivities during extreme temperature condition and transport of biomass burning plumes were 106.37±4.27 and 106.22±5.15 s−1, respectively, which are substantially higher than background level of 98.78±1.16 s−1. Multivariate analysis also clustered the compounds into five factors, which highlighted the sources of the unaccounted-for VOCs. Ultimately, results here underscore the effect of extreme heat and wildfire emissions on the overall chemical properties VOC in a temperate forest.

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Publication Details

Journal
Atmospheric chemistry and physics
Published
2025-11-24
DOI
https://doi.org/10.5194/acp-25-16611-2025
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
0.00

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article

Measurement report: Extreme heat and wildfire emissions enhance volatile organic compounds in a temperate forest

Melanie A. Mayes, Christian Mark Salvador, Lianhong Gu, Kevin R. Birdwell et al.
Atmospheric chemistry and physics
Atmospheric chemistry and aerosols
article

Measurement report: Extreme heat and wildfire emissions enhance volatile organic compounds in a temperate forest

Melanie A. Mayes, Christian Mark Salvador, Lianhong Gu, Kevin R. Birdwell, Jeffrey D. Wood, Emma Grace Cochran, Bella D. Kamplain, Hunter A. Seubert, Sami S. Overby
article en

Abstract

Abstract. Climate extremes are projected to cause unprecedented deviations in the emission and transformation of volatile organic compounds (VOCs), which trigger feedback mechanisms that will impact the atmospheric oxidation and formation of aerosols and clouds. However, the response of VOCs to future conditions such as extreme heat and wildfire events is still uncertain. This study explored the modification of the mixing ratio and distribution of several anthropogenic and biogenic VOCs in a temperate oak–hickory–juniper forest as a response to increased temperature and transported biomass burning plumes. A chemical ionization mass spectrometer was deployed on a tower at a height of 32 m in rural central Missouri, United States, for the continuous and in situ measurement of VOCs from June to August of 2023. The maximum observed temperature in the region was 38 °C, and during multiple episodes the temperature remained above 32 °C for several hours. Biogenic VOCs such as isoprene and monoterpene followed closely the temperature daily profile but at varying rates, whereas anthropogenic VOCs were insensitive to elevated temperature. During the measurement period, wildfire emissions were transported to the site and substantially increased the mixing ratios of acetonitrile and benzene, which are produced from burning of biomass. An in-depth analysis of the mass spectra revealed more than 250 minor compounds, such as formamide and methylglyoxal. Extreme heat and presence of wildfire plumes modified the overall volatility, reactivity, O : C, and H : C ratios of the extended list of VOCs. The calculated OH reactivities during extreme temperature condition and transport of biomass burning plumes were 106.37±4.27 and 106.22±5.15 s−1, respectively, which are substantially higher than background level of 98.78±1.16 s−1. Multivariate analysis also clustered the compounds into five factors, which highlighted the sources of the unaccounted-for VOCs. Ultimately, results here underscore the effect of extreme heat and wildfire emissions on the overall chemical properties VOC in a temperate forest.

Atmospheric chemistry and physicsVol. 25(22)
University College Dublin (IE), Oak Ridge National Laboratory (US), Lawrence Berkeley National Laboratory (US), University of Colorado Boulder (US), University of Colorado System (US), University of Missouri (US)
U.S. Department of Energy, U.S. Department of Agriculture, Battelle, University of Nebraska-Lincoln, UT-Battelle, National Oceanic and Atmospheric Administration, Office of Science, Biological and Environmental Research, Oak Ridge National Laboratory
Openalex Percentile: Top 59%
Atmospheric chemistry and aerosols
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