Diurnal cycles of short-lived tropospheric alkenes at a north Atlantic coastal site
Observation of diurnal cycles in atmospheric concentrations of reactive alkenes are reported from measurements performed at a North Atlantic coastal site (Mace Head, Eire 53°19′34″N; 9°54′14″W). Species seen to exhibit distinct cycles included isoprene, ethene, propene, 1-butene, iso-butene and a su...
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Veröffentlicht in: | Atmospheric environment (1994) 1999-07, Vol.33 (15), p.2417-2422 |
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creator | Lewis, A.C. McQuaid, J.B. Carslaw, N. Pilling, M.J. |
description | Observation of diurnal cycles in atmospheric concentrations of reactive alkenes are reported from measurements performed at a North Atlantic coastal site (Mace Head, Eire 53°19′34″N; 9°54′14″W). Species seen to exhibit distinct cycles included isoprene, ethene, propene, 1-butene, iso-butene and a substituted C
6 alkene. Five hundred and thirty air mass classified measurements were performed over a 4 week period at approximately hourly frequency and demonstrate that during periods when air flow resulted from unpolluted oceanic regions a clear daily cycle in concentrations existed, peaking at around solar noon for all species. These observations support the proposed mechanism of production via photochemical degradation of organic carbon in sea water. The observed concentrations showed strong correlation (propene
R
2>0.75) with solar flux, with little relationship to other meteorological or chemical parameters. The species’ short atmospheric lifetimes indicate that the source of emission was from local coastal waters within close proximity of the sampling site. At solar noon concentrations of reactive alkenes from oceanic sources were responsible for up to 88% of non-methane hydrocarbon reaction with the hydroxyl radical at this coastal marine site. |
doi_str_mv | 10.1016/S1352-2310(98)00429-4 |
format | Article |
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6 alkene. Five hundred and thirty air mass classified measurements were performed over a 4 week period at approximately hourly frequency and demonstrate that during periods when air flow resulted from unpolluted oceanic regions a clear daily cycle in concentrations existed, peaking at around solar noon for all species. These observations support the proposed mechanism of production via photochemical degradation of organic carbon in sea water. The observed concentrations showed strong correlation (propene
R
2>0.75) with solar flux, with little relationship to other meteorological or chemical parameters. The species’ short atmospheric lifetimes indicate that the source of emission was from local coastal waters within close proximity of the sampling site. At solar noon concentrations of reactive alkenes from oceanic sources were responsible for up to 88% of non-methane hydrocarbon reaction with the hydroxyl radical at this coastal marine site.</description><identifier>ISSN: 1352-2310</identifier><identifier>EISSN: 1873-2844</identifier><identifier>DOI: 10.1016/S1352-2310(98)00429-4</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Air mass origin ; alkenes ; Atlantic Ocean ; Chemical composition and interactions. Ionic interactions and processes ; Diurnal cycles ; Earth, ocean, space ; Exact sciences and technology ; External geophysics ; Hydroxyl radical chemistry ; Marine ; Meteorology ; Oceanic emissions ; Reactive alkene</subject><ispartof>Atmospheric environment (1994), 1999-07, Vol.33 (15), p.2417-2422</ispartof><rights>1999 Elsevier Science Ltd</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c429t-4e96932ba083b35f44a08af98709ea74a868a70e04e2101c7e9ab9bbe91ec3153</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1352231098004294$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1755955$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Lewis, A.C.</creatorcontrib><creatorcontrib>McQuaid, J.B.</creatorcontrib><creatorcontrib>Carslaw, N.</creatorcontrib><creatorcontrib>Pilling, M.J.</creatorcontrib><title>Diurnal cycles of short-lived tropospheric alkenes at a north Atlantic coastal site</title><title>Atmospheric environment (1994)</title><description>Observation of diurnal cycles in atmospheric concentrations of reactive alkenes are reported from measurements performed at a North Atlantic coastal site (Mace Head, Eire 53°19′34″N; 9°54′14″W). Species seen to exhibit distinct cycles included isoprene, ethene, propene, 1-butene, iso-butene and a substituted C
6 alkene. Five hundred and thirty air mass classified measurements were performed over a 4 week period at approximately hourly frequency and demonstrate that during periods when air flow resulted from unpolluted oceanic regions a clear daily cycle in concentrations existed, peaking at around solar noon for all species. These observations support the proposed mechanism of production via photochemical degradation of organic carbon in sea water. The observed concentrations showed strong correlation (propene
R
2>0.75) with solar flux, with little relationship to other meteorological or chemical parameters. The species’ short atmospheric lifetimes indicate that the source of emission was from local coastal waters within close proximity of the sampling site. At solar noon concentrations of reactive alkenes from oceanic sources were responsible for up to 88% of non-methane hydrocarbon reaction with the hydroxyl radical at this coastal marine site.</description><subject>Air mass origin</subject><subject>alkenes</subject><subject>Atlantic Ocean</subject><subject>Chemical composition and interactions. Ionic interactions and processes</subject><subject>Diurnal cycles</subject><subject>Earth, ocean, space</subject><subject>Exact sciences and technology</subject><subject>External geophysics</subject><subject>Hydroxyl radical chemistry</subject><subject>Marine</subject><subject>Meteorology</subject><subject>Oceanic emissions</subject><subject>Reactive alkene</subject><issn>1352-2310</issn><issn>1873-2844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkU1LAzEQhhdRsFZ_grAHET2sJptsk5yk1E8oeKiew2w6S6PbTU3SQv-96Yd47GkG5pl5Z-bNsktK7iihg_sJZVVZlIySGyVvCeGlKvhR1qNSsKKUnB-n_A85zc5C-CKEMKFEL5s82qXvoM3N2rQYctfkYeZ8LFq7wmkevVu4sJihtyaH9hu7xEDMIe8SNMuHsYUupppxEGIaE2zE8-ykgTbgxT72s8_np4_RazF-f3kbDceFSRvGgqMaKFbWQCSrWdVwnjJolBREIQgOciBBECQcy3SnEaigVnWNiqJhtGL97Ho3d-HdzxJD1HMbDLZpJXTLoKkkKgnQw6BgYkAZOwzyinLJRAKrHWi8C8FjoxfezsGvNSV6Y4remqI3H9dK6q0pmqe-q70ABANt46EzNvw3i6pS1eayhx2G6X0ri14HY7EzOLUeTdRTZw8I_QK5V5_7</recordid><startdate>19990701</startdate><enddate>19990701</enddate><creator>Lewis, A.C.</creator><creator>McQuaid, J.B.</creator><creator>Carslaw, N.</creator><creator>Pilling, M.J.</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7TN</scope><scope>7TV</scope><scope>F1W</scope><scope>H96</scope><scope>H97</scope><scope>L.G</scope><scope>7TG</scope><scope>KL.</scope></search><sort><creationdate>19990701</creationdate><title>Diurnal cycles of short-lived tropospheric alkenes at a north Atlantic coastal site</title><author>Lewis, A.C. ; McQuaid, J.B. ; Carslaw, N. ; Pilling, M.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c429t-4e96932ba083b35f44a08af98709ea74a868a70e04e2101c7e9ab9bbe91ec3153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Air mass origin</topic><topic>alkenes</topic><topic>Atlantic Ocean</topic><topic>Chemical composition and interactions. Ionic interactions and processes</topic><topic>Diurnal cycles</topic><topic>Earth, ocean, space</topic><topic>Exact sciences and technology</topic><topic>External geophysics</topic><topic>Hydroxyl radical chemistry</topic><topic>Marine</topic><topic>Meteorology</topic><topic>Oceanic emissions</topic><topic>Reactive alkene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lewis, A.C.</creatorcontrib><creatorcontrib>McQuaid, J.B.</creatorcontrib><creatorcontrib>Carslaw, N.</creatorcontrib><creatorcontrib>Pilling, M.J.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Pollution Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy & Non-Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><jtitle>Atmospheric environment (1994)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lewis, A.C.</au><au>McQuaid, J.B.</au><au>Carslaw, N.</au><au>Pilling, M.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diurnal cycles of short-lived tropospheric alkenes at a north Atlantic coastal site</atitle><jtitle>Atmospheric environment (1994)</jtitle><date>1999-07-01</date><risdate>1999</risdate><volume>33</volume><issue>15</issue><spage>2417</spage><epage>2422</epage><pages>2417-2422</pages><issn>1352-2310</issn><eissn>1873-2844</eissn><abstract>Observation of diurnal cycles in atmospheric concentrations of reactive alkenes are reported from measurements performed at a North Atlantic coastal site (Mace Head, Eire 53°19′34″N; 9°54′14″W). Species seen to exhibit distinct cycles included isoprene, ethene, propene, 1-butene, iso-butene and a substituted C
6 alkene. Five hundred and thirty air mass classified measurements were performed over a 4 week period at approximately hourly frequency and demonstrate that during periods when air flow resulted from unpolluted oceanic regions a clear daily cycle in concentrations existed, peaking at around solar noon for all species. These observations support the proposed mechanism of production via photochemical degradation of organic carbon in sea water. The observed concentrations showed strong correlation (propene
R
2>0.75) with solar flux, with little relationship to other meteorological or chemical parameters. The species’ short atmospheric lifetimes indicate that the source of emission was from local coastal waters within close proximity of the sampling site. At solar noon concentrations of reactive alkenes from oceanic sources were responsible for up to 88% of non-methane hydrocarbon reaction with the hydroxyl radical at this coastal marine site.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/S1352-2310(98)00429-4</doi><tpages>6</tpages></addata></record> |
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subjects | Air mass origin alkenes Atlantic Ocean Chemical composition and interactions. Ionic interactions and processes Diurnal cycles Earth, ocean, space Exact sciences and technology External geophysics Hydroxyl radical chemistry Marine Meteorology Oceanic emissions Reactive alkene |
title | Diurnal cycles of short-lived tropospheric alkenes at a north Atlantic coastal site |
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