001     186715
005     20240712100955.0
024 7 _ |2 doi
|a 10.5194/acp-15-799-2015
024 7 _ |2 ISSN
|a 1680-7316
024 7 _ |2 ISSN
|a 1680-7324
024 7 _ |2 WOS
|a WOS:000351170000005
037 _ _ |a FZJ-2015-00787
082 _ _ |a 550
100 1 _ |0 P:(DE-HGF)0
|a Oswald, R.
|b 0
|e Corresponding Author
245 _ _ |a A comparison of HONO budgets for two measurement heights at a field station within the boreal forest in Finland
260 _ _ |a Katlenburg-Lindau
|b EGU
|c 2015
336 7 _ |0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
|a Journal Article
|b journal
|m journal
|s 1422019209_24935
336 7 _ |2 DataCite
|a Output Types/Journal article
336 7 _ |0 0
|2 EndNote
|a Journal Article
336 7 _ |2 BibTeX
|a ARTICLE
336 7 _ |2 ORCID
|a JOURNAL_ARTICLE
336 7 _ |2 DRIVER
|a article
520 _ _ |a Atmospheric concentrations of nitrous acid (HONO), one of the major precursors of the hydroxyl radical (OH) in the troposphere, significantly exceed the values predicted by the assumption of a photostationary state (PSS) during daytime. Therefore, additional sources of HONO were intensively investigated in the last decades. This study presents budget calculations of HONO based on simultaneous measurements of all relevant species, including HONO and OH at two different measurement heights, i.e. 1 m above the ground and about 2 to 3 m above the canopy (24 m above the ground), conducted in a boreal forest environment. We observed mean HONO concentrations of about 6.5 × 108 molecules cm−3 (26 ppt) during daytime, more than 20 times higher than expected from the PSS of 0.2 × 108 molecules cm−3 (1 ppt). To close the budgets at both heights, a strong additional source term during daytime is required. This unidentified source is at its maximum at noon (up to 1.1 × 106 molecules cm−3 s−1, 160 ppt h−1) and in general up to 2.3 times stronger above the canopy than close to the ground. The insignificance of known gas phase reactions and other processes like dry deposition or advection compared to the photolytic decomposition of HONO at this measurement site was an ideal prerequisite to study possible correlations of this unknown term to proposed HONO sources. But neither the proposed emissions from soils nor the proposed photolysis of adsorbed HNO3 contributed substantially to the unknown source. However, the unknown source was found to be perfectly correlated to the unbalanced photolytic loss of HONO.
536 _ _ |0 G:(DE-HGF)POF3-243
|a 243 - Tropospheric trace substances and their transformation processes (POF3-243)
|c POF3-243
|f POF III
|x 0
588 _ _ |a Dataset connected to CrossRef, juser.fz-juelich.de
700 1 _ |0 P:(DE-HGF)0
|a Ermel, M.
|b 1
700 1 _ |0 P:(DE-HGF)0
|a Hens, K.
|b 2
700 1 _ |0 P:(DE-HGF)0
|a Novelli, A.
|b 3
700 1 _ |0 P:(DE-HGF)0
|a Ouwersloot, H. G.
|b 4
700 1 _ |0 P:(DE-HGF)0
|a Paasonen, P.
|b 5
700 1 _ |0 P:(DE-HGF)0
|a Petäjä, T.
|b 6
700 1 _ |0 P:(DE-HGF)0
|a Sipilä, M.
|b 7
700 1 _ |0 P:(DE-HGF)0
|a Keronen, P.
|b 8
700 1 _ |0 P:(DE-HGF)0
|a Bäck, J.
|b 9
700 1 _ |0 P:(DE-HGF)0
|a Königstedt, R.
|b 10
700 1 _ |0 P:(DE-HGF)0
|a Hosaynali Beygi, Z.
|b 11
700 1 _ |0 P:(DE-HGF)0
|a Fischer, H.
|b 12
700 1 _ |0 P:(DE-Juel1)2693
|a Bohn, B.
|b 13
|u fzj
700 1 _ |0 P:(DE-HGF)0
|a Kubistin, D.
|b 14
700 1 _ |0 P:(DE-HGF)0
|a Harder, H.
|b 15
700 1 _ |0 P:(DE-HGF)0
|a Martinez, M.
|b 16
700 1 _ |0 P:(DE-HGF)0
|a Williams, J.
|b 17
700 1 _ |0 P:(DE-HGF)0
|a Hoffmann, T.
|b 18
700 1 _ |0 P:(DE-HGF)0
|a Trebs, I.
|b 19
700 1 _ |0 P:(DE-HGF)0
|a Sörgel, M.
|b 20
773 _ _ |0 PERI:(DE-600)2069847-1
|a 10.5194/acp-15-799-2015
|g Vol. 15, no. 2, p. 799 - 813
|n 2
|p 799 - 813
|t Atmospheric chemistry and physics
|v 15
|x 1680-7324
|y 2015
856 4 _ |u https://juser.fz-juelich.de/record/186715/files/FZJ-2015-00787.pdf
|y OpenAccess
909 C O |o oai:juser.fz-juelich.de:186715
|p openaire
|p open_access
|p driver
|p VDB:Earth_Environment
|p VDB
|p dnbdelivery
910 1 _ |0 I:(DE-588b)5008462-8
|6 P:(DE-Juel1)2693
|a Forschungszentrum Jülich GmbH
|b 13
|k FZJ
913 0 _ |0 G:(DE-HGF)POF2-233
|1 G:(DE-HGF)POF2-230
|2 G:(DE-HGF)POF2-200
|a DE-HGF
|b Erde und Umwelt
|l Atmosphäre und Klima
|v Trace gas and aerosol processes in the troposphere
|x 0
913 1 _ |0 G:(DE-HGF)POF3-243
|1 G:(DE-HGF)POF3-240
|2 G:(DE-HGF)POF3-200
|a DE-HGF
|l Atmosphäre und Klima
|v Tropospheric trace substances and their transformation processes
|x 0
|4 G:(DE-HGF)POF
|3 G:(DE-HGF)POF3
|b Erde und Umwelt
914 1 _ |y 2015
915 _ _ |0 LIC:(DE-HGF)CCBY3
|2 HGFVOC
|a Creative Commons Attribution CC BY 3.0
915 _ _ |0 StatID:(DE-HGF)0100
|2 StatID
|a JCR
915 _ _ |0 StatID:(DE-HGF)0110
|2 StatID
|a WoS
|b Science Citation Index
915 _ _ |0 StatID:(DE-HGF)0111
|2 StatID
|a WoS
|b Science Citation Index Expanded
915 _ _ |0 StatID:(DE-HGF)0150
|2 StatID
|a DBCoverage
|b Web of Science Core Collection
915 _ _ |0 StatID:(DE-HGF)0199
|2 StatID
|a DBCoverage
|b Thomson Reuters Master Journal List
915 _ _ |0 StatID:(DE-HGF)0200
|2 StatID
|a DBCoverage
|b SCOPUS
915 _ _ |0 StatID:(DE-HGF)0300
|2 StatID
|a DBCoverage
|b Medline
915 _ _ |0 StatID:(DE-HGF)0500
|2 StatID
|a DBCoverage
|b DOAJ
915 _ _ |0 StatID:(DE-HGF)1150
|2 StatID
|a DBCoverage
|b Current Contents - Physical, Chemical and Earth Sciences
915 _ _ |0 StatID:(DE-HGF)9905
|2 StatID
|a IF >= 5
920 _ _ |l yes
920 1 _ |0 I:(DE-Juel1)IEK-8-20101013
|k IEK-8
|l Troposphäre
|x 0
980 1 _ |a FullTexts
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-Juel1)IEK-8-20101013
980 _ _ |a UNRESTRICTED
980 _ _ |a FullTexts
981 _ _ |a I:(DE-Juel1)ICE-3-20101013


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21