Source apportionment of chlorinated polycyclic aromatic hydrocarbons associated with ambient particles in a Japanese megacity
Chlorinated polycyclic aromatic hydrocarbons (ClPAHs) are novel species of environmental contaminants whose possible sources remain unclear. The occurrence of ClPAHs within total suspended particles (TSP) is compared with weekly air samples at two sites of differing characteristics (industrial and r...
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description | Chlorinated polycyclic aromatic hydrocarbons (ClPAHs) are novel species of environmental contaminants whose possible sources remain unclear. The occurrence of ClPAHs within total suspended particles (TSP) is compared with weekly air samples at two sites of differing characteristics (industrial and residential) in the megacity of Nagoya, Japan. Samples were collected over 12 months during 2011–2012. All 24 species of targeted ClPAHs were detected at both industrial and residential sites, where mean concentrations of total ClPAHs in TSP were 20.7 and 14.1 pg/m
3
, respectively. High concentrations at the industrial site were frequently observed during winter, suggesting potent seasonal ClPAH sources there. Positive matrix factorization modeling of particulate ClPAH source identification and apportioning were conducted for datasets including ClPAHs, PAHs, elements and ions, plus elemental carbons in TSP. Eight factors were identified as possible ClPAH sources, with estimates that the dominant one was a specific source of ClPAH emission (31%), followed by traffic (23%), photodegradable and semi-volatile species (18%), long-range transport (11%), and industry and oil combustion (10%). Source contributions of ClPAHs differed substantially from those of PAHs. This suggests specific and/or potent ClPAH sources in the local area, and that the production mechanisms between ClPAHs and PAHs are substantially different. |
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3
, respectively. High concentrations at the industrial site were frequently observed during winter, suggesting potent seasonal ClPAH sources there. Positive matrix factorization modeling of particulate ClPAH source identification and apportioning were conducted for datasets including ClPAHs, PAHs, elements and ions, plus elemental carbons in TSP. Eight factors were identified as possible ClPAH sources, with estimates that the dominant one was a specific source of ClPAH emission (31%), followed by traffic (23%), photodegradable and semi-volatile species (18%), long-range transport (11%), and industry and oil combustion (10%). Source contributions of ClPAHs differed substantially from those of PAHs. This suggests specific and/or potent ClPAH sources in the local area, and that the production mechanisms between ClPAHs and PAHs are substantially different.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep38358</identifier><identifier>PMID: 27922081</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>704/172/169/895 ; 704/172/4081 ; Air sampling ; Airborne particulates ; Chlorinated hydrocarbons ; Contaminants ; Humanities and Social Sciences ; Megacities ; multidisciplinary ; Polycyclic aromatic hydrocarbons ; Science ; Species</subject><ispartof>Scientific reports, 2016-12, Vol.6 (1), p.38358-38358, Article 38358</ispartof><rights>The Author(s) 2016</rights><rights>Copyright Nature Publishing Group Dec 2016</rights><rights>Copyright © 2016, The Author(s) 2016 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-3842ef4d501fd36b8a3dfd3d373291d03cce88b2bd1d9af5b80e825ade54808f3</citedby><cites>FETCH-LOGICAL-c438t-3842ef4d501fd36b8a3dfd3d373291d03cce88b2bd1d9af5b80e825ade54808f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5138597/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5138597/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27922081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kamiya, Yuta</creatorcontrib><creatorcontrib>Iijima, Akihiro</creatorcontrib><creatorcontrib>Ikemori, Fumikazu</creatorcontrib><creatorcontrib>Okuda, Tomoaki</creatorcontrib><creatorcontrib>Ohura, Takeshi</creatorcontrib><title>Source apportionment of chlorinated polycyclic aromatic hydrocarbons associated with ambient particles in a Japanese megacity</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Chlorinated polycyclic aromatic hydrocarbons (ClPAHs) are novel species of environmental contaminants whose possible sources remain unclear. The occurrence of ClPAHs within total suspended particles (TSP) is compared with weekly air samples at two sites of differing characteristics (industrial and residential) in the megacity of Nagoya, Japan. Samples were collected over 12 months during 2011–2012. All 24 species of targeted ClPAHs were detected at both industrial and residential sites, where mean concentrations of total ClPAHs in TSP were 20.7 and 14.1 pg/m
3
, respectively. High concentrations at the industrial site were frequently observed during winter, suggesting potent seasonal ClPAH sources there. Positive matrix factorization modeling of particulate ClPAH source identification and apportioning were conducted for datasets including ClPAHs, PAHs, elements and ions, plus elemental carbons in TSP. Eight factors were identified as possible ClPAH sources, with estimates that the dominant one was a specific source of ClPAH emission (31%), followed by traffic (23%), photodegradable and semi-volatile species (18%), long-range transport (11%), and industry and oil combustion (10%). Source contributions of ClPAHs differed substantially from those of PAHs. This suggests specific and/or potent ClPAH sources in the local area, and that the production mechanisms between ClPAHs and PAHs are substantially different.</description><subject>704/172/169/895</subject><subject>704/172/4081</subject><subject>Air sampling</subject><subject>Airborne particulates</subject><subject>Chlorinated hydrocarbons</subject><subject>Contaminants</subject><subject>Humanities and Social Sciences</subject><subject>Megacities</subject><subject>multidisciplinary</subject><subject>Polycyclic aromatic hydrocarbons</subject><subject>Science</subject><subject>Species</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNplkU1v1DAQhi1ERavSA38AWeICSAv-iBPnglRVfKpSD8DZmtiTXVeJHewsKAf-O95uWS3UF480jx7P-CXkGWdvOJP6bU44SS2VfkTOBKvUSkghHh_Vp-Qi51tWjhJtxdsn5FQ0rRBM8zPy-2vcJosUpimm2ccwYphp7KndDDH5ADM6OsVhsYsdvKWQ4ghzKTaLS9FC6mLIFHKO1t-xv_y8oTB2fueZoDjtgJn6QIF-gQkCZqQjrsH6eXlKTnoYMl7c3-fk-4f3364-ra5vPn6-urxe2UrqeSV1JbCvnGK8d7LuNEhXCicbKVrumLQWte5E57hroVedZqiFAoeq0kz38py823unbTeis2W2BIOZkh8hLSaCN_92gt-YdfxpFJdatU0RvLwXpPhji3k2o88Wh6HsE7fZcF3VstZNLQr64j_0tnxxKOsVqm1l3TTVTvhqT9kUc4mwPwzDmdnlag65Fvb58fQH8m-KBXi9B3JphTWmoycf2P4AF9ywlA</recordid><startdate>20161206</startdate><enddate>20161206</enddate><creator>Kamiya, Yuta</creator><creator>Iijima, Akihiro</creator><creator>Ikemori, Fumikazu</creator><creator>Okuda, Tomoaki</creator><creator>Ohura, Takeshi</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20161206</creationdate><title>Source apportionment of chlorinated polycyclic aromatic hydrocarbons associated with ambient particles in a Japanese megacity</title><author>Kamiya, Yuta ; Iijima, Akihiro ; Ikemori, Fumikazu ; Okuda, Tomoaki ; Ohura, Takeshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-3842ef4d501fd36b8a3dfd3d373291d03cce88b2bd1d9af5b80e825ade54808f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>704/172/169/895</topic><topic>704/172/4081</topic><topic>Air sampling</topic><topic>Airborne particulates</topic><topic>Chlorinated hydrocarbons</topic><topic>Contaminants</topic><topic>Humanities and Social Sciences</topic><topic>Megacities</topic><topic>multidisciplinary</topic><topic>Polycyclic aromatic hydrocarbons</topic><topic>Science</topic><topic>Species</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kamiya, Yuta</creatorcontrib><creatorcontrib>Iijima, Akihiro</creatorcontrib><creatorcontrib>Ikemori, Fumikazu</creatorcontrib><creatorcontrib>Okuda, Tomoaki</creatorcontrib><creatorcontrib>Ohura, Takeshi</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kamiya, Yuta</au><au>Iijima, Akihiro</au><au>Ikemori, Fumikazu</au><au>Okuda, Tomoaki</au><au>Ohura, Takeshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Source apportionment of chlorinated polycyclic aromatic hydrocarbons associated with ambient particles in a Japanese megacity</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2016-12-06</date><risdate>2016</risdate><volume>6</volume><issue>1</issue><spage>38358</spage><epage>38358</epage><pages>38358-38358</pages><artnum>38358</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Chlorinated polycyclic aromatic hydrocarbons (ClPAHs) are novel species of environmental contaminants whose possible sources remain unclear. The occurrence of ClPAHs within total suspended particles (TSP) is compared with weekly air samples at two sites of differing characteristics (industrial and residential) in the megacity of Nagoya, Japan. Samples were collected over 12 months during 2011–2012. All 24 species of targeted ClPAHs were detected at both industrial and residential sites, where mean concentrations of total ClPAHs in TSP were 20.7 and 14.1 pg/m
3
, respectively. High concentrations at the industrial site were frequently observed during winter, suggesting potent seasonal ClPAH sources there. Positive matrix factorization modeling of particulate ClPAH source identification and apportioning were conducted for datasets including ClPAHs, PAHs, elements and ions, plus elemental carbons in TSP. Eight factors were identified as possible ClPAH sources, with estimates that the dominant one was a specific source of ClPAH emission (31%), followed by traffic (23%), photodegradable and semi-volatile species (18%), long-range transport (11%), and industry and oil combustion (10%). Source contributions of ClPAHs differed substantially from those of PAHs. This suggests specific and/or potent ClPAH sources in the local area, and that the production mechanisms between ClPAHs and PAHs are substantially different.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>27922081</pmid><doi>10.1038/srep38358</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 704/172/169/895 704/172/4081 Air sampling Airborne particulates Chlorinated hydrocarbons Contaminants Humanities and Social Sciences Megacities multidisciplinary Polycyclic aromatic hydrocarbons Science Species |
title | Source apportionment of chlorinated polycyclic aromatic hydrocarbons associated with ambient particles in a Japanese megacity |
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