- 1Utrecht University, Institute for Marine and Atmospheric Research Utrecht, Physics, Utrecht, Netherlands (t.rockmann@uu.nl)
- 2Atmospheric Chemistry Department, Max Planck Institute for Chemistry, Hahn-Meitner-Weg 1, 55128 Mainz, Germany
- 3Acacia Impact Innovation, 5384 BB Heesch, The Netherlands
- 4Max Planck Institute for Biogeochemistry, Hans-Knöll-Str.10, 07745 Jena, Germany
- 5Department of Atmospheric Chemistry and Climate, Institute of Physical Chemistry Blas Cabrera, Spanish National Research Council (CSIC), 28006 Madrid, Spain
- 6National Institute of Water & Atmospheric Research Ltd (NIWA), Hataitai, Wellington 6021, New Zealand
- 7Cooperative Institute for Research in Environmental Sciences - University of Colorado
- 8Department of Chemistry, University of Copenhagen, DK-2100 Copenhagen Ø, Denmark
- 9Environmental and Climate Lab - CNR-ISAC Lamezia Terme, Italy
- *A full list of authors appears at the end of the abstract
Carbon monoxide (CO) is an important indirect greenhouse gas, plays a key intermediate role in the cycling of carbon compounds in the atmosphere and via these reactions affects the atmospheric oxidation capacity. Its sources and sinks can be (partially) distinguished with isotope measurements, but extensive observations of CO isotopic composition are sparse. A network of independent global observatories monitored 𝛿13CCO and 𝛿 18OCO at the turn of the 21st century. Since this time, the sole continuous monitoring of CO isotopic composition has been carried out at Baring Head, New Zealand. Starting in 2023, as part of the ISAMO project, we have resumed regular measurements of 𝛿13CCO and 𝛿 18OCO at seven global monitoring stations, with a focus on the tropical Atlantic. The goal of ISAMO is to better constrain the proposed pathway of methane removal via chlorine radicals that can be released photochemically from mixed mineral dust - salt aerosols. Here we use the new and existing CO isotope data together with model simulations to derive empirical constraints for the production rate of CO from the CH4 + Cl reaction. In addition, we will demonstrate how CO isotope measurements can be used to constrain long-term, and episodic, changes in the global and regional CO budget, arguing for sustaining such measurements at globally distributed locations.
Africa Barreto, Natalia Prats, Ignacio Mármol, Ramón Ramos, Jesús M Arrieta, Helder Timas, Dickon Young, Viviana Horna, Susan Trumbore, Peter Sealy, Berend van de Kraats
How to cite: Röckmann, T., Brashear, C., Gromos, S., van Herpen, M., Yu, X., van der Veen, C., van Asperen, H., Zaehle, S., Moossen, H., Jordan, A., Meidan, D., Saiz-Lopez, A., Sperlich, P., Moss, R., Mak, J., Petron, G., Crotwell, A., Johnson, M., and D'Amico, F. and the The ISAMO team: Using stable isotope of measurements of carbon monoxide for constraining short- and long-term changes in its global budget and atmospheric chemistry, EGU General Assembly 2026, Vienna, Austria, 3–8 May 2026, EGU26-21821, https://doi.org/10.5194/egusphere-egu26-21821, 2026.