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dc.contributor.authorZhao, T.
dc.contributor.authorMao, J.
dc.contributor.authorSimpson, W.R.
dc.contributor.authorDe Smedt, I.
dc.contributor.authorZhu, L.
dc.contributor.authorHanisco, T.F.
dc.contributor.authorWolfe, G.M.
dc.contributor.authorSt. Clair, J.M.
dc.contributor.authorGonzález Abad, G.
dc.contributor.authorNowlan, C.R.
dc.contributor.authorBarletta, B.
dc.contributor.authorMeinardi, S.
dc.contributor.authorBlake, D.R.
dc.contributor.authorApel, E.C.
dc.contributor.authorHornbrook, R.S.
dc.date2022
dc.date.accessioned2022-12-23T17:27:01Z
dc.date.available2022-12-23T17:27:01Z
dc.identifier.urihttps://orfeo.belnet.be/handle/internal/10714
dc.descriptionHere we use satellite observations of formaldehyde (HCHO) vertical column densities (VCD) from the TROPOspheric Monitoring Instrument (TROPOMI), aircraft measurements, combined with a nested regional chemical transport model (GEOS-Chem at 0,5 x 0,625° resolution), to better understand the variability and sources of summertime HCHO in Alaska. We first evaluate GEOS-Chem with in-situ airborne measurements during the Atmospheric Tomography Mission 1 (ATom-1) aircraft campaign. We show reasonable agreement between observed and modeled HCHO, isoprene, monoterpenes and the sum of methyl vinyl ketone and methacrolein (MVK+MACR) in the continental boundary layer. In particular, HCHO profiles show spatial homogeneity in Alaska, suggesting a minor contribution of biogenic emissions to HCHO VCD. We further examine the TROPOMI HCHO product in Alaska in summer, reprocessed by GEOS-Chem model output for a priori profiles and shape factors. For years with low wildfire activity (e.g., 2018), we find that HCHO VCDs are largely dominated by background HCHO (58 %–71 %), with minor contributions from wildfires (20 %–32 %) and biogenic VOC emissions (8 %–10 %). For years with intense wildfires (e.g., 2019), summertime HCHO VCD is dominated by wildfire emissions (50 %–72 %), with minor contributions from background (22 %–41 %) and biogenic VOCs (6 %–10 %). In particular, the model indicates a major contribution of wildfires from direct emissions of HCHO, instead of secondary production of HCHO from oxidation of larger VOCs. We find that the column contributed by biogenic VOC is often small and below the TROPOMI detection limit, in part due to the slow HCHO production from isoprene oxidation under low NOx conditions. This work highlights challenges for quantifying HCHO and its precursors in remote pristine regions.
dc.languageeng
dc.titleSource and variability of formaldehyde (HCHO) at northern high latitudes: an integrated satellite, aircraft, and model study
dc.typeArticle
dc.subject.frascatiPhysical sciences
dc.audienceScientific
dc.source.titleAtmospheric Chemistry and Physics
dc.source.volume22
dc.source.issue11
dc.source.page7163-7178
Orfeo.peerreviewedYes
dc.identifier.doi10.5194/acp-22-7163-2022
dc.identifier.scopus


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