Estimation of the fossil fuel component in atmospheric CO₂ based on radiocarbon measurements at the Beromünster tall tower, Switzerland
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Description
Fossil fuel CO₂ (CO₂ff/ is the major contributor of anthropogenic CO₂ in the atmosphere, and accurate quantification is essential to better understand the carbon cycle. Since October 2012, we have been continuously measuring the mixing ratios of CO, CO₂, CH₄, and H₂O at five different heights at the Beromünster tall tower, Switzerland. Air samples
for radiocarbon (Δ¹⁴CO₂) analysis have also been collected from the highest sampling inlet (212.5 m) of the tower on a biweekly basis. A correction was applied for ¹⁴CO₂ emissions from nearby nuclear power plants (NPPs), which have been simulated with the Lagrangian transport model FLEXPART-COSMO. The ¹⁴CO₂ emissions from NPPs offset the depletion in ¹⁴C by fossil fuel emissions, resulting in an underestimation of the fossil fuel component in atmospheric CO₂ by about 16 %. An average observed ratio (RCO) of 13.4±1.3 mmol mol⁻¹ was calculated from the enhancements in CO mixing ratios relative to the clean-air reference site Jungfraujoch (ΔCO) and the radiocarbon-based fossil fuel CO₂ mole fractions. The wintertime RCO estimate of 12.5±3.3 is about 30% higher than the wintertime ratio between in situ measured CO and CO2 enhancements at Beromünster over the Jungfraujoch background (8.7 mmol mol⁻¹) corrected for non-fossil contributions due to strong biospheric contribution despite the strong correlation between ΔCO and ΔCO₂ in winter. By combining the ratio derived using the radiocarbon measurements and the in situ measured CO mixing ratios, a high-resolution time series of CO₂ff was calculated exhibiting a clear seasonality driven by seasonal variability in emissions and vertical mixing. By
subtracting the fossil fuel component and the large-scale background, we have determined the regional biospheric CO₂ component that is characterized by seasonal variations ranging between -15 and +30 ppm. A pronounced diurnal variation was observed during summer modulated by biospheric exchange and vertical mixing, while no consistent pattern was found during winter.
for radiocarbon (Δ¹⁴CO₂) analysis have also been collected from the highest sampling inlet (212.5 m) of the tower on a biweekly basis. A correction was applied for ¹⁴CO₂ emissions from nearby nuclear power plants (NPPs), which have been simulated with the Lagrangian transport model FLEXPART-COSMO. The ¹⁴CO₂ emissions from NPPs offset the depletion in ¹⁴C by fossil fuel emissions, resulting in an underestimation of the fossil fuel component in atmospheric CO₂ by about 16 %. An average observed ratio (RCO) of 13.4±1.3 mmol mol⁻¹ was calculated from the enhancements in CO mixing ratios relative to the clean-air reference site Jungfraujoch (ΔCO) and the radiocarbon-based fossil fuel CO₂ mole fractions. The wintertime RCO estimate of 12.5±3.3 is about 30% higher than the wintertime ratio between in situ measured CO and CO2 enhancements at Beromünster over the Jungfraujoch background (8.7 mmol mol⁻¹) corrected for non-fossil contributions due to strong biospheric contribution despite the strong correlation between ΔCO and ΔCO₂ in winter. By combining the ratio derived using the radiocarbon measurements and the in situ measured CO mixing ratios, a high-resolution time series of CO₂ff was calculated exhibiting a clear seasonality driven by seasonal variability in emissions and vertical mixing. By
subtracting the fossil fuel component and the large-scale background, we have determined the regional biospheric CO₂ component that is characterized by seasonal variations ranging between -15 and +30 ppm. A pronounced diurnal variation was observed during summer modulated by biospheric exchange and vertical mixing, while no consistent pattern was found during winter.
Date of Publication
2017
Publication Type
Article
Subject(s)
Language(s)
en
Contributor(s)
Szidat, Sonke | |
Brunner, Dominik | |
Satar, Ece | |
Schanda, Rudiger | |
Nyfeler, Peter | |
Battaglia, Michael | |
Steinbacher, Martin | |
Hammer, Samuel |
Series
Atmospheric chemistry and physics Discussions
Publisher
European Geosciences Union
ISSN
1680-7375
Access(Rights)
open.access