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Wavelength-dependent isotope fractionation in visible light O3 photolysis and atmospheric implications

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Taraborrelli,  Domenico
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Gromov,  Sergey
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Citation

Früchtl, M., Janssen, C., Taraborrelli, D., Gromov, S., & Röckmann, T. (2015). Wavelength-dependent isotope fractionation in visible light O3 photolysis and atmospheric implications. Geophysical Research Letters, 42(20), 8711-8718. doi:10.1002/2015GL066219.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0029-2A0C-2
Abstract
The O-17 and O-18 isotope fractionation associated with photolysis of O-3 in the Chappuis band was determined using a broadband light source with cutoff filters at 455, 550, and 620 nm and narrowband light sources at 530, 617, and 660 nm. The isotope effects follow a mass- dependent fractionation pattern ( delta O-17/delta O-18 = 0.53). Contrary to theoretical predictions, fractionations are negative for all wavelength ranges investigated and do not change signs at the absorption cross-section maximum. Our measurements differ from theoretical calculations by as much as 34% in (18)epsilon(O3+hv) = ((18)J/(16)J - 1). The wavelength dependence is also weaker than predicted. Photo-induced fractionation is strongest when using a low-wavelength cutoff at 620 nm with (18)epsilon(O3+hv) = -26.9(+/- 1.4)parts per thousand. With decreasing wavelength, fractionation values diminish to (18)epsilon(O3+hv) = -12.9(+/- 1.3)parts per thousand at 530 nm. Results from an atmospheric model demonstrate that visible light photolysis is the most important tropospheric sink of O-3, which thus contributes about one sixth to the ozone enrichment.