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Evidence of formation of submicrometer water‐soluble organic aerosols at a deciduous forest site in northern Japan in summer

Identifieur interne : 000E51 ( Istex/Corpus ); précédent : 000E50; suivant : 000E52

Evidence of formation of submicrometer water‐soluble organic aerosols at a deciduous forest site in northern Japan in summer

Auteurs : Yuzo Miyazaki ; Jinsang Jung ; Pingqing Fu ; Yasuko Mizoguchi ; Katsumi Yamanoi ; Kimitaka Kawamura

Source :

RBID : ISTEX:9D892DFB9EF11470FA11B1F60E9C3F184E63EF2C

Abstract

Semicontinuous measurements of submicrometer water‐soluble organic aerosols and particle size distributions were conducted at a deciduous forest site in northern Japan in August 2010. Increases in particle number concentration were frequently observed in daytime, accompanied by an increase in the concentrations of water‐soluble organic carbon (WSOC). We found that daily averaged WSOC concentrations positively correlated with gross primary production of CO2 by the forest ecosystem (r2 = 0.63) and ambient temperature during daytime. These relations suggest that the formation of WSOC is closely linked to photosynthetic activity by the forest ecosystem, which depends on both temperature and solar radiation. Off‐line chemical analysis of samples of particles with aerodynamic diameter smaller than 1 μm collected during a 2 day event of elevated WSOC levels suggests that photochemical aging of both α‐ andβ‐pinene and isoprene oxidation products contributes to the particle growth and the WSOC mass. Organic tracers of primary biological aerosol particles (PBAPs) showed distinct diurnal variations with a maximum around noontime, also indicating that higher temperature and light intensity induce emissions of PBAPs. However, their contribution to the submicrometer WSOC mass was likely insignificant. During the day, the concentrations of 3‐methyl‐1,2,3‐butanetricarboxylic acid (3‐MBTCA) showed a strong dependence on temperature, and the ratios of WSOC to particle volume concentration increased with an increase in the concentration ratios of 3‐MBTCA to pinonic acid (PA). This result supports a previous proposal that the 3‐MBTCA/PA ratios in submicrometer particles can be a useful tracer for chemical aging of biogenic secondary organic aerosol from forest vegetation.

Url:
DOI: 10.1029/2012JD018250

Links to Exploration step

ISTEX:9D892DFB9EF11470FA11B1F60E9C3F184E63EF2C

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<p xml:id="jgrd18040-para-0001" label="1">Semicontinuous measurements of submicrometer water‐soluble organic aerosols and particle size distributions were conducted at a deciduous forest site in northern Japan in August 2010. Increases in particle number concentration were frequently observed in daytime, accompanied by an increase in the concentrations of water‐soluble organic carbon (WSOC). We found that daily averaged WSOC concentrations positively correlated with gross primary production of CO
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<abstract>Semicontinuous measurements of submicrometer water‐soluble organic aerosols and particle size distributions were conducted at a deciduous forest site in northern Japan in August 2010. Increases in particle number concentration were frequently observed in daytime, accompanied by an increase in the concentrations of water‐soluble organic carbon (WSOC). We found that daily averaged WSOC concentrations positively correlated with gross primary production of CO2 by the forest ecosystem (r2 = 0.63) and ambient temperature during daytime. These relations suggest that the formation of WSOC is closely linked to photosynthetic activity by the forest ecosystem, which depends on both temperature and solar radiation. Off‐line chemical analysis of samples of particles with aerodynamic diameter smaller than 1 μm collected during a 2 day event of elevated WSOC levels suggests that photochemical aging of both α‐ andβ‐pinene and isoprene oxidation products contributes to the particle growth and the WSOC mass. Organic tracers of primary biological aerosol particles (PBAPs) showed distinct diurnal variations with a maximum around noontime, also indicating that higher temperature and light intensity induce emissions of PBAPs. However, their contribution to the submicrometer WSOC mass was likely insignificant. During the day, the concentrations of 3‐methyl‐1,2,3‐butanetricarboxylic acid (3‐MBTCA) showed a strong dependence on temperature, and the ratios of WSOC to particle volume concentration increased with an increase in the concentration ratios of 3‐MBTCA to pinonic acid (PA). This result supports a previous proposal that the 3‐MBTCA/PA ratios in submicrometer particles can be a useful tracer for chemical aging of biogenic secondary organic aerosol from forest vegetation.</abstract>
<abstract type="short">Formation of PM1 WSOC is linked to photosynthesis by the forest ecosystem Biogenic SOA significantly contributed to particle growth of PM1 WSOC Alpha‐pinene SOA and WSOC formation depends on temperature in daytime</abstract>
<note type="additional physical form">Tab‐delimited Table 1.</note>
<subject>
<genre>keywords</genre>
<topic>biogenic organic aerosols</topic>
<topic>decidous forest</topic>
<topic>water‐soluble organic carbon</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>Journal of Geophysical Research: Atmospheres</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>J. Geophys. Res.</title>
</titleInfo>
<genre type="journal">journal</genre>
<subject>
<genre>index-terms</genre>
<topic authorityURI="http://psi.agu.org/subset/AAC">Aerosol and Clouds</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/0300">ATMOSPHERIC COMPOSITION AND STRUCTURE</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/0305">Aerosols and particles</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/0315">Biosphere/atmosphere interactions</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/0322">Constituent sources and sinks</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/0365">Troposphere: composition and chemistry</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/0345">Pollution: urban and regional</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/0400">BIOGEOSCIENCES</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/0426">Biosphere/atmosphere interactions</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/1600">GLOBAL CHANGE</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/1610">Atmosphere</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/4800">OCEANOGRAPHY: BIOLOGICAL AND CHEMICAL</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/4801">Aerosols</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/4900">PALEOCEANOGRAPHY</topic>
<topic authorityURI="http://psi.agu.org/taxonomy5/4906">Aerosols</topic>
</subject>
<subject>
<genre>article-category</genre>
<topic>Aerosol and Clouds</topic>
</subject>
<identifier type="ISSN">0148-0227</identifier>
<identifier type="eISSN">2156-2202</identifier>
<identifier type="DOI">10.1002/(ISSN)2156-2202d</identifier>
<identifier type="CODEN">JGREA2</identifier>
<identifier type="PublisherID">JGRD</identifier>
<part>
<date>2012</date>
<detail type="volume">
<caption>vol.</caption>
<number>117</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>D19</number>
</detail>
<extent unit="pages">
<start>n/a</start>
<end>n/a</end>
<total>12</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">9D892DFB9EF11470FA11B1F60E9C3F184E63EF2C</identifier>
<identifier type="DOI">10.1029/2012JD018250</identifier>
<identifier type="ArticleID">2012JD018250</identifier>
<accessCondition type="use and reproduction" contentType="copyright">©2012. American Geophysical Union. All Rights Reserved.</accessCondition>
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<recordContentSource>WILEY</recordContentSource>
</recordInfo>
</mods>
</metadata>
<serie></serie>
</istex>
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