GSTDTAP  > 地球科学
DOI10.5194/acp-17-8837-2017
Organic carbon at a remote site of the western Mediterranean Basin: sources and chemistry during the ChArMEx SOP2 field experiment
Michoud, Vincent1,2; Sciare, Jean3,4; Sauvage, Stephane1; Dusanter, Sebastien1,6; Leonardis, Thierry1; Gros, Valerie3,4; Kalogridis, Cerise3,4; Zannoni, Nora3,4; Feron, Anais3,4; Petit, Jean-Eudes3,4,7,13; Crenn, Vincent3,4; Baisnee, Dominique3,4; Sarda-Esteve, Roland3,4; Bonnaire, Nicolas4; Marchand, Nicolas8; DeWitt, H. Langley8; Pey, Jorge8,14; Colomb, Aurelie9; Gheusi, Francois10; Szidat, Sonke11,12; Stavroulas, Iasonas5; Borbon, Agnes2,15; Locoge, Nadine1
2017-07-21
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2017
卷号17期号:14
文章类型Article
语种英语
国家France; Cyprus; USA; Switzerland; Spain
英文摘要

The ChArMEx (Chemistry and Aerosols Mediterranean Experiments) SOP2 (special observation period 2) field campaign took place from 15 July to 5 August 2013 in the western Mediterranean Basin at Ersa, a remote site in Cape Corse. During the campaign more than 80 volatile organic compounds (VOCs), including oxygenated species, were measured by different online and offline techniques. At the same time, an exhaustive description of the chemical composition of fine aerosols was performed with an aerosol chemical speciation monitor (ACSM). Low levels of anthropogenic VOCs (typically tens to hundreds of parts per trillion for individual species) and black carbon (0.1-0.9 mu gm(-3)) were observed, while significant levels of biogenic species (peaking at the ppb level) were measured. Furthermore, secondary oxygenated VOCs (OVOCs) largely dominated the VOC speciation during the campaign, while organic matter (OM) dominated the aerosol chemical composition, representing 55% of the total mass of non-refractory PM1 on average (average of 3.74 +/- 1.80 mu gm(-3)), followed by sulfate (27 %, 1.83 +/- 1.06 mu gm(-3)), ammonium (13 %, 0.90 +/- 0.55 mu gm(-3)) and nitrate (5 %, 0.31 +/- 0.18 mu gm(-3)).


Positive matrix factorization (PMF) and concentration field (CF) analyses were performed on a database containing 42 VOCs (or grouped VOCs), including OVOCs, to identify the covariation factors of compounds that are representative of primary emissions or chemical transformation processes. A six-factor solution was found for the PMF analysis, including a primary and secondary biogenic factor correlated with temperature and exhibiting a clear diurnal profile. In addition, three anthropogenic factors characterized by compounds with various lifetimes and/or sources have been identified (long-lived, medium-lived and short-lived anthropogenic factors). The anthropogenic nature of these factors was confirmed by the CF analysis, which identified potential source areas known for intense anthropogenic emissions (north of Italy and southeast of France). Finally, a factor characterized by OVOCs of both biogenic and anthropogenic origin was found. This factor was well correlated with submicron organic aerosol (OA) measured by an aerosol chemical speciation monitor (ACSM), highlighting the close link between OVOCs and organic aerosols; the latter is mainly associated (96 %) with the secondary OA fraction. The source apportionment of OA measured by ACSM led to a three-factor solution identified as hydrogenlike OA (HOA), semi-volatile oxygenated OA (SV-OOA) and low volatility OOA (LV-OOA) for averaged mass concentrations of 0.13, 1.59 and 1.92 mu gm(-3), respectively.


A combined analysis of gaseous PMF factors with inorganic and organic fractions of aerosols helped distinguish between anthropogenic continental and biogenic influences on the aerosol-and gas-phase compositions.


领域地球科学
收录类别SCI-E
WOS记录号WOS:000406152100001
WOS关键词POSITIVE MATRIX FACTORIZATION ; SOURCE-RECEPTOR RELATIONSHIPS ; PROTON-TRANSFER-REACTION ; TALL TOWER MEASUREMENTS ; LONG-TERM MEASUREMENTS ; TIME-OF-FLIGHT ; SOURCE APPORTIONMENT ; OXALIC-ACID ; CHEMICAL-CHARACTERIZATION ; ATMOSPHERIC CHEMISTRY
WOS类目Environmental Sciences ; Meteorology & Atmospheric Sciences
WOS研究方向Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences
引用统计
文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/30438
专题地球科学
作者单位1.Univ Lille, IMT Lille Douai, SAGE, Dept Sci Atmosphere & Genie Environm, F-59000 Lille, France;
2.UPD, UPEC, IPSL, LISA,CNRS,UMR7583, Creteil, France;
3.CEA, IPSL, LSCE, St Quentin en Yvelines, France;
4.Univ Versailles, CNRS, St Quentin en Yvelines, France;
5.Cyprus Inst, Energy Environm & Water Res Ctr, Nicosia, Cyprus;
6.Indiana Univ, Sch Publ & Environm Affairs, Bloomington, IN USA;
7.INERIS, F-60550 Verneuil En Halatte, France;
8.Aix Marseille Univ, CNRS, LCE, Marseille, France;
9.Univ Blaise Pascal, Clermont Univ, CNRS, LaMP,UMR6016, Aubiere, France;
10.Univ Toulouse, CNRS, Lab Aerol, Toulouse, France;
11.Univ Bern, Dept Chem & Biochem, Bern, Switzerland;
12.Univ Bern, Oeschger Ctr Climate Change Res, Bern, Switzerland;
13.Air Lorraine, 20 Rue Pierre Simon Laplace, F-57070 Metz, France;
14.Geol Survey Spain, Zaragoza 50006, Spain;
15.Univ Blaise Pascal, Clermont Univ, LaMP, CNRS,UMR6016, Aubiere, France
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GB/T 7714
Michoud, Vincent,Sciare, Jean,Sauvage, Stephane,et al. Organic carbon at a remote site of the western Mediterranean Basin: sources and chemistry during the ChArMEx SOP2 field experiment[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2017,17(14).
APA Michoud, Vincent.,Sciare, Jean.,Sauvage, Stephane.,Dusanter, Sebastien.,Leonardis, Thierry.,...&Locoge, Nadine.(2017).Organic carbon at a remote site of the western Mediterranean Basin: sources and chemistry during the ChArMEx SOP2 field experiment.ATMOSPHERIC CHEMISTRY AND PHYSICS,17(14).
MLA Michoud, Vincent,et al."Organic carbon at a remote site of the western Mediterranean Basin: sources and chemistry during the ChArMEx SOP2 field experiment".ATMOSPHERIC CHEMISTRY AND PHYSICS 17.14(2017).
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