Articles | Volume 15, issue 11
https://doi.org/10.5194/bg-15-3277-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/bg-15-3277-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Stomatal control of leaf fluxes of carbonyl sulfide and CO2 in a Typha freshwater marsh
Department of Atmospheric and Oceanic Sciences, University of
California, Los Angeles, CA 90095-1565, USA
Kadmiel Maseyk
School of Environment, Earth and Ecosystem Sciences, The Open
University, Milton Keynes MK7 6AA, UK
formerly at: Institute of Ecology and Environmental Sciences,
Université Pierre et Marie Curie, Paris 6, France
Céline Lett
Laboratoire des Sciences du Climat et de l'Environnement,
Université Paris Saclay, 91191 Gif-sur-Yvette, France
formerly at: Institute of Ecology and Environmental Sciences,
Université Pierre et Marie Curie, Paris 6, France
Department of Atmospheric and Oceanic Sciences, University of
California, Los Angeles, CA 90095-1565, USA
formerly at: Institute of Ecology and Environmental Sciences,
Université Pierre et Marie Curie, Paris 6, France
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Cited
16 citations as recorded by crossref.
- Influences of light and humidity on carbonyl sulfide-based estimates of photosynthesis L. Kooijmans et al. https://doi.org/10.1073/pnas.1807600116
- Leaf relative uptake of carbonyl sulfide to CO2 seen through the lens of stomatal conductance–photosynthesis coupling W. Sun et al. https://doi.org/10.1111/nph.18178
- Simultaneous removal of hydrogen sulfide and carbonyl sulfide from various sulfur-containing gases: a review J. Hu et al. https://doi.org/10.1039/D6RA03730E
- Intercomparison of methods to estimate gross primary production based on CO2 and COS flux measurements K. Kohonen et al. https://doi.org/10.5194/bg-19-4067-2022
- Predictions of Entropy and Gibbs Energy for Carbonyl Sulfide C. Jia et al. https://doi.org/10.1021/acsomega.9b02950
- Terrestrial photosynthesis inferred from plant carbonyl sulfide uptake J. Lai et al. https://doi.org/10.1038/s41586-024-08050-3
- Refining the shuttleworth-wallace model with particle swarm optimization and genetic algorithm for evapotranspiration simulation in the ecotone of the eastern margin of the tibetan plateau Z. Weihang et al. https://doi.org/10.1016/j.catena.2026.110014
- Reviews and syntheses: Turning the challenges of partitioning ecosystem evaporation and transpiration into opportunities P. Stoy et al. https://doi.org/10.5194/bg-16-3747-2019
- Seasonal Evolution of Canopy Stomatal Conductance for a Prairie and Maize Field in the Midwestern United States from Continuous Carbonyl Sulfide Fluxes M. Berkelhammer et al. https://doi.org/10.1029/2019GL085652
- Carbonyl sulfide: comparing a mechanistic representation of the vegetation uptake in a land surface model and the leaf relative uptake approach F. Maignan et al. https://doi.org/10.5194/bg-18-2917-2021
- Light and Water Conditions Co-Regulated Stomata and Leaf Relative Uptake Rate (LRU) during Photosynthesis and COS Assimilation: A Meta-Analysis P. Wang et al. https://doi.org/10.3390/su14052840
- Tracking canopy conductance and transpiration of CAM-plants Agave sisalana with carbonyl sulfide fluxes K. Kohonen et al. https://doi.org/10.1016/j.agrformet.2025.110966
- Evaluation of carbonyl sulfide biosphere exchange in the Simple Biosphere Model (SiB4) L. Kooijmans et al. https://doi.org/10.5194/bg-18-6547-2021
- Restricted internal diffusion weakens transpiration–photosynthesis coupling during heatwaves: Evidence from leaf carbonyl sulphide exchange W. Sun et al. https://doi.org/10.1111/pce.14840
- Reply to: The size of tropical vegetation gross primary production J. Lai et al. https://doi.org/10.1038/s41586-026-10561-0
- Technical note: Novel estimates of the leaf relative uptake rate of carbonyl sulfide from optimality theory G. Wohlfahrt et al. https://doi.org/10.5194/bg-20-589-2023
16 citations as recorded by crossref.
- Influences of light and humidity on carbonyl sulfide-based estimates of photosynthesis L. Kooijmans et al. https://doi.org/10.1073/pnas.1807600116
- Leaf relative uptake of carbonyl sulfide to CO2 seen through the lens of stomatal conductance–photosynthesis coupling W. Sun et al. https://doi.org/10.1111/nph.18178
- Simultaneous removal of hydrogen sulfide and carbonyl sulfide from various sulfur-containing gases: a review J. Hu et al. https://doi.org/10.1039/D6RA03730E
- Intercomparison of methods to estimate gross primary production based on CO2 and COS flux measurements K. Kohonen et al. https://doi.org/10.5194/bg-19-4067-2022
- Predictions of Entropy and Gibbs Energy for Carbonyl Sulfide C. Jia et al. https://doi.org/10.1021/acsomega.9b02950
- Terrestrial photosynthesis inferred from plant carbonyl sulfide uptake J. Lai et al. https://doi.org/10.1038/s41586-024-08050-3
- Refining the shuttleworth-wallace model with particle swarm optimization and genetic algorithm for evapotranspiration simulation in the ecotone of the eastern margin of the tibetan plateau Z. Weihang et al. https://doi.org/10.1016/j.catena.2026.110014
- Reviews and syntheses: Turning the challenges of partitioning ecosystem evaporation and transpiration into opportunities P. Stoy et al. https://doi.org/10.5194/bg-16-3747-2019
- Seasonal Evolution of Canopy Stomatal Conductance for a Prairie and Maize Field in the Midwestern United States from Continuous Carbonyl Sulfide Fluxes M. Berkelhammer et al. https://doi.org/10.1029/2019GL085652
- Carbonyl sulfide: comparing a mechanistic representation of the vegetation uptake in a land surface model and the leaf relative uptake approach F. Maignan et al. https://doi.org/10.5194/bg-18-2917-2021
- Light and Water Conditions Co-Regulated Stomata and Leaf Relative Uptake Rate (LRU) during Photosynthesis and COS Assimilation: A Meta-Analysis P. Wang et al. https://doi.org/10.3390/su14052840
- Tracking canopy conductance and transpiration of CAM-plants Agave sisalana with carbonyl sulfide fluxes K. Kohonen et al. https://doi.org/10.1016/j.agrformet.2025.110966
- Evaluation of carbonyl sulfide biosphere exchange in the Simple Biosphere Model (SiB4) L. Kooijmans et al. https://doi.org/10.5194/bg-18-6547-2021
- Restricted internal diffusion weakens transpiration–photosynthesis coupling during heatwaves: Evidence from leaf carbonyl sulphide exchange W. Sun et al. https://doi.org/10.1111/pce.14840
- Reply to: The size of tropical vegetation gross primary production J. Lai et al. https://doi.org/10.1038/s41586-026-10561-0
- Technical note: Novel estimates of the leaf relative uptake rate of carbonyl sulfide from optimality theory G. Wohlfahrt et al. https://doi.org/10.5194/bg-20-589-2023
Saved (final revised paper)
Discussed (final revised paper)
Latest update: 04 Aug 2026
Short summary
Carbonyl sulfide (COS) is an emerging tracer to probe land photosynthesis at canopy to global scales, but the relationship between leaf COS and CO2 fluxes needed for this application is poorly quantified. With in situ leaf fluxes of COS and CO2 measured in a freshwater marsh, we show that light and vapor deficit control the relationship between leaf COS and CO2 fluxes by regulating stomatal conductance. Our findings support the use of COS as a tracer for canopy photosynthesis.
Carbonyl sulfide (COS) is an emerging tracer to probe land photosynthesis at canopy to global...
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