Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-7796
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dc.contributor.authorKampf, Christopher Johannes-
dc.contributor.authorCorrigan, Ashley L.-
dc.contributor.authorJohnson, A. M.-
dc.contributor.authorSong, W.-
dc.contributor.authorKeronen, P.-
dc.contributor.authorKönigstedt, Rainer-
dc.contributor.authorWilliams, Jonathan-
dc.contributor.authorRussell, L. M.-
dc.contributor.authorPetäjä, T.-
dc.contributor.authorFischer, H.-
dc.contributor.authorHoffmann, Thorsten-
dc.date.accessioned2022-10-04T08:14:00Z-
dc.date.available2022-10-04T08:14:00Z-
dc.date.issued2012-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7811-
dc.description.abstractThe first dataset for summertime boreal forest concentrations of two atmospherically relevant α-dicarbonyl compounds, glyoxal (Gly) and methylglyoxal (Mgly) on PM<sub>2.5</sub> aerosol was obtained during the HUMPPA-COPEC-2010 field measurement intensive in Hyytiälä, Finland. Anthropogenic influences over the course of the campaign were identified using trace gas signatures and aerosol particle chemical composition analysis. The data evaluation allowed the identification of different events such as urban pollution plumes, biomass burning and sawmill emissions as sources of high Gly and Mgly concentrations. Mean aerosol concentrations during periods of biogenic influence were 0.81 ng m<sup>−3</sup> for Gly and 0.31 ng m<sup>−3</sup> for Mgly. Mgly was generally less abundant in PM<sub>2.5</sub>, probably due to its shorter photolysis lifetime and less effective partitioning into the particle phase due to its smaller effective Henry's Law constant compared to Gly. This is in contrast with previous urban studies which show significantly more Mgly than Gly. Peak concentrations for Gly coincided with nearby sources, e.g. high VOC emissions from nearby sawmills, urban pollution plumes from the city of Tampere located 50 km southwest of the sampling site and biomass burning emissions from wildfires. Calculated ratios of Gly in PM<sub>2.5</sub> and total organic matter in PM1 aerosols indicate higher values in less aged aerosols. Irreversible processing of Gly in the particle phase, e.g. via oxidation by OH radicals, organo sulfate or imidazole formation are processes currently discussed in the literature which could likely explain these findings.de_DE
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizinde
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleFirst measurements of reactive α-dicarbonyl concentrations on PM<sub>2.5</sub> aerosol over the Boreal forest in Finland during HUMPPA-COPEC 2010 - source apportionment and links to aerosol agingde_DE
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-7796-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.number7950-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleAtmospheric chemistry and physicsde
jgu.journal.volume12de
jgu.journal.issue14de
jgu.pages.start6145de
jgu.pages.end6155de
jgu.publisher.year2012-
jgu.publisher.nameEuropean Geosciences Unionde
jgu.publisher.placeKatlenburg-Lindaude
jgu.publisher.urihttp://dx.doi.org/10.5194/acp-12-6145-2012de
jgu.publisher.issn1680-7324de
jgu.publisher.issn1680-7316de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
opus.date.modified2019-08-16T09:48:45Z-
opus.subject.dfgcode09-313-
opus.organisation.stringFB 09: Chemie, Pharmazie und Geowissenschaften: Institut für Anorganische Chemie und Analytische Chemiede_DE
opus.identifier.opusid22717-
opus.institute.number0903-
opus.metadataonlyfalse-
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_EN
opus.affiliatedKampf, Christopher Johannes-
opus.affiliatedHoffmann, Thorsten-
jgu.publisher.doi10.5194/acp-12-6145-2012de
jgu.organisation.rorhttps://ror.org/023b0x485-
Appears in collections:DFG-OA-Publizieren (2012 - 2017)

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