Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/85
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dc.contributor.authorSinha, V.-
dc.date.accessioned2013-04-30T07:58:50Z-
dc.date.available2013-04-30T07:58:50Z-
dc.date.issued2011-
dc.identifier.citationAtmos. Chem. Phys., 11, pp.,9709-9719en_US
dc.identifier.urihttp://www.atmos-chem-phys.net/11/9709/2011/acp-11-9709-2011.htmlen_US
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractWe have modelled the total atmospheric OH- reactivity in a boreal forest and investigated the individ- ual contributions from gas phase inorganic species, iso- prene, monoterpenes, and methane along with other impor- tant VOCs. Daily and seasonal variation in OH-reactivity for the year 2008 was examined as well as the vertical OH- reactivity profile. We have used SOSA; a one dimensional vertical chemistry-transport model (Boy et al., 2011a) to- gether with measurements from Hyyti ̈ l ̈ , SMEAR II station, aa Southern Finland, conducted in August 2008. Model sim- ulations only account for ∼30–50 % of the total measured OH sink, and in our opinion, the reason for missing OH- reactivity is due to unmeasured unknown BVOCs, and limi- tations in our knowledge of atmospheric chemistry including uncertainties in rate constants. Furthermore, we found that the OH-reactivity correlates with both organic and inorganic compounds and increases during summer. The summertime canopy level OH-reactivity peaks during night and the verti- cal OH-reactivity decreases with height.en_US
dc.language.isoenen_US
dc.titleModelling atmospheric OH-reactivity in a boreal forest ecosystem,en_US
dc.typeArticleen_US
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