Chemical composition of size-segregated aerosols in Lhasa city, Tibetan Plateau
To reveal the chemical characteristics of size-segregated aerosols in the high-altitude city of Tibetan Plateau, eight-size aerosol samples were collected in Lhasa from March 2013 to February 2014. The annual mean of online PM2.5 was 25.0±16.0μgm−3, which was much lower than Asian cities but similar...
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description | To reveal the chemical characteristics of size-segregated aerosols in the high-altitude city of Tibetan Plateau, eight-size aerosol samples were collected in Lhasa from March 2013 to February 2014. The annual mean of online PM2.5 was 25.0±16.0μgm−3, which was much lower than Asian cities but similar with some European cities. The annual mean concentrations of organic carbon (OC, 7.92μgm−3 in PM2.1 and 12.66μgm−3 in PM9.0) and elemental carbon (EC, 1.00μgm−3 in PM2.1 and 1.21μgm−3 in PM9.0) in Lhasa aerosols were considerably lower than those heavily polluted cities such as Beijing and Xi'an, China and Kathmandu, Nepal. Sulfate, NO3−, NH4+ and Ca2+ were 0.75±0.31, 0.82±0.35, 0.38±0.34 and 0.57±0.29μgm−3 in fine particles while in coarse particles they were 0.57±0.37, 0.73±0.23, 0.07±0.03 and 2.52±1.37μgm−3, respectively. Secondary water-soluble ions composed 35.8% of the total ionic components in fine particles according to the established electroneutrality, while in coarse particles they took up only 9.3%. Ca2+ (40.6%) was the major component of the coarse particles. For seasonality, the concentrations of OC, EC, SO42−, NH4+, K+, Ca2+, Mg2+, Cl− and Na+ presented higher values during late autumn and winter but were relatively lower in spring and summer. Nevertheless, NO3− was considerably higher in summer and autumn, presumably due to increased tourist-vehicle emissions. During winter and spring, [Ca2+]/[NO3−+SO42−] ratios in coarse particles showed higher values of 7.31 and 6.17, respectively, emphasizing the dust influence. [NO3−]/[SO42−] ratios in fine particles during spring, summer and autumn exceeding 1 indicated that the currently predominant vehicle exhaust makes a greater contribution to the aerosols. While more stationary sources such as coal and biomass burning existed in winter since the [NO3−]/[SO42−] ratio was less than 1. Different sources and formation processes lead to a bimodal size distribution (0–0.65μm in fine particles and 4.7–9.0μm in coarse particles) for all of the compounds except Na+.
•OC and EC in Lhasa aerosols were considerably lower than other Chinese cities.•Secondary water-soluble ions accounted for higher proportionality in fine particles than coarse particles.•Ca2+ contributed to a large fraction of the ionic species in the coarse particles.•Most of the chemical compounds exhibited bimodal size-distribution patterns. |
doi_str_mv | 10.1016/j.atmosres.2016.02.005 |
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•OC and EC in Lhasa aerosols were considerably lower than other Chinese cities.•Secondary water-soluble ions accounted for higher proportionality in fine particles than coarse particles.•Ca2+ contributed to a large fraction of the ionic species in the coarse particles.•Most of the chemical compounds exhibited bimodal size-distribution patterns.</description><identifier>ISSN: 0169-8095</identifier><identifier>EISSN: 1873-2895</identifier><identifier>DOI: 10.1016/j.atmosres.2016.02.005</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Atmospheric aerosols ; Lhasa ; OC/EC ; Size distribution ; WSIs</subject><ispartof>Atmospheric research, 2016-06, Vol.174-175, p.142-150</ispartof><rights>2016 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-37318db20373e2c195c8cb505b52536e0d522f1536839aaee124d6a6b8e9ce423</citedby><cites>FETCH-LOGICAL-c411t-37318db20373e2c195c8cb505b52536e0d522f1536839aaee124d6a6b8e9ce423</cites><orcidid>0000-0002-7545-5611</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.atmosres.2016.02.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids></links><search><creatorcontrib>Wan, Xin</creatorcontrib><creatorcontrib>Kang, Shichang</creatorcontrib><creatorcontrib>Xin, Jinyuan</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><creatorcontrib>Wen, Tianxue</creatorcontrib><creatorcontrib>Wang, Pengling</creatorcontrib><creatorcontrib>Wang, Yuesi</creatorcontrib><creatorcontrib>Cong, Zhiyuan</creatorcontrib><title>Chemical composition of size-segregated aerosols in Lhasa city, Tibetan Plateau</title><title>Atmospheric research</title><description>To reveal the chemical characteristics of size-segregated aerosols in the high-altitude city of Tibetan Plateau, eight-size aerosol samples were collected in Lhasa from March 2013 to February 2014. The annual mean of online PM2.5 was 25.0±16.0μgm−3, which was much lower than Asian cities but similar with some European cities. The annual mean concentrations of organic carbon (OC, 7.92μgm−3 in PM2.1 and 12.66μgm−3 in PM9.0) and elemental carbon (EC, 1.00μgm−3 in PM2.1 and 1.21μgm−3 in PM9.0) in Lhasa aerosols were considerably lower than those heavily polluted cities such as Beijing and Xi'an, China and Kathmandu, Nepal. Sulfate, NO3−, NH4+ and Ca2+ were 0.75±0.31, 0.82±0.35, 0.38±0.34 and 0.57±0.29μgm−3 in fine particles while in coarse particles they were 0.57±0.37, 0.73±0.23, 0.07±0.03 and 2.52±1.37μgm−3, respectively. Secondary water-soluble ions composed 35.8% of the total ionic components in fine particles according to the established electroneutrality, while in coarse particles they took up only 9.3%. Ca2+ (40.6%) was the major component of the coarse particles. For seasonality, the concentrations of OC, EC, SO42−, NH4+, K+, Ca2+, Mg2+, Cl− and Na+ presented higher values during late autumn and winter but were relatively lower in spring and summer. Nevertheless, NO3− was considerably higher in summer and autumn, presumably due to increased tourist-vehicle emissions. During winter and spring, [Ca2+]/[NO3−+SO42−] ratios in coarse particles showed higher values of 7.31 and 6.17, respectively, emphasizing the dust influence. [NO3−]/[SO42−] ratios in fine particles during spring, summer and autumn exceeding 1 indicated that the currently predominant vehicle exhaust makes a greater contribution to the aerosols. While more stationary sources such as coal and biomass burning existed in winter since the [NO3−]/[SO42−] ratio was less than 1. Different sources and formation processes lead to a bimodal size distribution (0–0.65μm in fine particles and 4.7–9.0μm in coarse particles) for all of the compounds except Na+.
•OC and EC in Lhasa aerosols were considerably lower than other Chinese cities.•Secondary water-soluble ions accounted for higher proportionality in fine particles than coarse particles.•Ca2+ contributed to a large fraction of the ionic species in the coarse particles.•Most of the chemical compounds exhibited bimodal size-distribution patterns.</description><subject>Atmospheric aerosols</subject><subject>Lhasa</subject><subject>OC/EC</subject><subject>Size distribution</subject><subject>WSIs</subject><issn>0169-8095</issn><issn>1873-2895</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPwzAQhC0EEuXxF5CPHEiwndi1b6CKl1SpHMrZcpxN6yqJi-0ilV-Pq8KZ085qZ1aaD6EbSkpKqLjflCYNPgaIJct7SVhJCD9BEyqnVcGk4qdokg-qkETxc3QR44ZkB6nVBC1maxicNT22ftj66JLzI_Ydju4bigirACuToMUGgo--j9iNeL420WDr0v4OL10DyYz4vc82s7tCZ53pI1z_zkv08fy0nL0W88XL2-xxXtia0lRU04rKtmEkC2CWKm6lbTjhDWe8EkBazlhHs5SVMgaAsroVRjQSlIWaVZfo9vh3G_znDmLSg4sW-t6M4HdR06nkrBZEiWwVR6vNDTKmTm-DG0zYa0r0gaDe6D-C-kBQE6Yznxx8OAYhF_lyEHS0DkYLrQtgk269--_FDxHofVM</recordid><startdate>20160615</startdate><enddate>20160615</enddate><creator>Wan, Xin</creator><creator>Kang, Shichang</creator><creator>Xin, Jinyuan</creator><creator>Liu, Bin</creator><creator>Wen, Tianxue</creator><creator>Wang, Pengling</creator><creator>Wang, Yuesi</creator><creator>Cong, Zhiyuan</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7TG</scope><scope>7TV</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H96</scope><scope>KL.</scope><scope>L.G</scope><scope>SOI</scope><orcidid>https://orcid.org/0000-0002-7545-5611</orcidid></search><sort><creationdate>20160615</creationdate><title>Chemical composition of size-segregated aerosols in Lhasa city, Tibetan Plateau</title><author>Wan, Xin ; Kang, Shichang ; Xin, Jinyuan ; Liu, Bin ; Wen, Tianxue ; Wang, Pengling ; Wang, Yuesi ; Cong, Zhiyuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-37318db20373e2c195c8cb505b52536e0d522f1536839aaee124d6a6b8e9ce423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Atmospheric aerosols</topic><topic>Lhasa</topic><topic>OC/EC</topic><topic>Size distribution</topic><topic>WSIs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wan, Xin</creatorcontrib><creatorcontrib>Kang, Shichang</creatorcontrib><creatorcontrib>Xin, Jinyuan</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><creatorcontrib>Wen, Tianxue</creatorcontrib><creatorcontrib>Wang, Pengling</creatorcontrib><creatorcontrib>Wang, Yuesi</creatorcontrib><creatorcontrib>Cong, Zhiyuan</creatorcontrib><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Pollution Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy & Non-Living Resources</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Environment Abstracts</collection><jtitle>Atmospheric research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wan, Xin</au><au>Kang, Shichang</au><au>Xin, Jinyuan</au><au>Liu, Bin</au><au>Wen, Tianxue</au><au>Wang, Pengling</au><au>Wang, Yuesi</au><au>Cong, Zhiyuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemical composition of size-segregated aerosols in Lhasa city, Tibetan Plateau</atitle><jtitle>Atmospheric research</jtitle><date>2016-06-15</date><risdate>2016</risdate><volume>174-175</volume><spage>142</spage><epage>150</epage><pages>142-150</pages><issn>0169-8095</issn><eissn>1873-2895</eissn><abstract>To reveal the chemical characteristics of size-segregated aerosols in the high-altitude city of Tibetan Plateau, eight-size aerosol samples were collected in Lhasa from March 2013 to February 2014. The annual mean of online PM2.5 was 25.0±16.0μgm−3, which was much lower than Asian cities but similar with some European cities. The annual mean concentrations of organic carbon (OC, 7.92μgm−3 in PM2.1 and 12.66μgm−3 in PM9.0) and elemental carbon (EC, 1.00μgm−3 in PM2.1 and 1.21μgm−3 in PM9.0) in Lhasa aerosols were considerably lower than those heavily polluted cities such as Beijing and Xi'an, China and Kathmandu, Nepal. Sulfate, NO3−, NH4+ and Ca2+ were 0.75±0.31, 0.82±0.35, 0.38±0.34 and 0.57±0.29μgm−3 in fine particles while in coarse particles they were 0.57±0.37, 0.73±0.23, 0.07±0.03 and 2.52±1.37μgm−3, respectively. Secondary water-soluble ions composed 35.8% of the total ionic components in fine particles according to the established electroneutrality, while in coarse particles they took up only 9.3%. Ca2+ (40.6%) was the major component of the coarse particles. For seasonality, the concentrations of OC, EC, SO42−, NH4+, K+, Ca2+, Mg2+, Cl− and Na+ presented higher values during late autumn and winter but were relatively lower in spring and summer. Nevertheless, NO3− was considerably higher in summer and autumn, presumably due to increased tourist-vehicle emissions. During winter and spring, [Ca2+]/[NO3−+SO42−] ratios in coarse particles showed higher values of 7.31 and 6.17, respectively, emphasizing the dust influence. [NO3−]/[SO42−] ratios in fine particles during spring, summer and autumn exceeding 1 indicated that the currently predominant vehicle exhaust makes a greater contribution to the aerosols. While more stationary sources such as coal and biomass burning existed in winter since the [NO3−]/[SO42−] ratio was less than 1. Different sources and formation processes lead to a bimodal size distribution (0–0.65μm in fine particles and 4.7–9.0μm in coarse particles) for all of the compounds except Na+.
•OC and EC in Lhasa aerosols were considerably lower than other Chinese cities.•Secondary water-soluble ions accounted for higher proportionality in fine particles than coarse particles.•Ca2+ contributed to a large fraction of the ionic species in the coarse particles.•Most of the chemical compounds exhibited bimodal size-distribution patterns.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.atmosres.2016.02.005</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7545-5611</orcidid></addata></record> |
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subjects | Atmospheric aerosols Lhasa OC/EC Size distribution WSIs |
title | Chemical composition of size-segregated aerosols in Lhasa city, Tibetan Plateau |
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