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Total OH reactivity changes over the Amazon rainforest during an El Niño event

MPG-Autoren
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Pfannerstill,  Eva Y.
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Nölscher,  Anke C.
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Yáñez-Serrano,  Ana Maria
Biogeochemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Bourtsoukidis,  Efstratios
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Keßel,  Stephan
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Tsokankunku,  Anywhere
Biogeochemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Wolff,  Stefan
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Sörgel,  Matthias
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Walter,  David
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Kesselmeier,  Jürgen
Biogeochemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Williams,  Jonathan
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Zitation

Pfannerstill, E. Y., Nölscher, A. C., Yáñez-Serrano, A. M., Bourtsoukidis, E., Keßel, S., Janssen, R. H., et al. (2018). Total OH reactivity changes over the Amazon rainforest during an El Niño event. Frontiers in Forests and Global Change, 1: 12. doi:10.3389/ffgc.2018.00012.


Zitierlink: https://hdl.handle.net/21.11116/0000-0003-0B6F-6
Zusammenfassung
The 2015/16 El Niño event caused unprecedented drought and warming in the Amazon basin. How tropical forests react to such extreme events in terms of volatile organic compound (VOC) emissions is of interest as the frequency of these events is predicted to increase through climate change. The diverse VOCs emitted can be significant for plants’ carbon budgets, influence ozone and particle production, and through their reactivity impact OH concentrations. Total OH reactivity is a directly measureable quantity that gives the reaction frequency of OH radicals with all reactive species in the atmosphere in s-1. Here we present a comparison of the OH reactivity diel cycle from November 2015, i.e. extreme drought and elevated temperatures associated with strong El Niño conditions, with November 2012, a “normal” El Niño Southern Oscillation (ENSO)-neutral period. Interestingly, the diel maximum of OH reactivity during the El Niño event occurred at sunset instead of, under normal conditions, early afternoon. The absolute total diel OH reactivity, however, did not change significantly. Daytime OH reactivity averages were 24.3 ± 14.5 s-1 in 2012 and 24.6 ± 11.9 s-1 in 2015, respectively. Our findings suggest that a combination of stronger turbulent transport above the canopy with stress-related monoterpene and, possibly, other biogenic volatile organic compound (BVOC) emissions were responsible for this increased reactivity at sunset.