GSTDTAP
DOI10.5194/acp-19-14677-2019
Regional sources of airborne ultrafine particle number and mass concentrations in California
Yu, Xin1; Venecek, Melissa2; Kumar, Anikender1; Hu, Jianlin3; Tanrikulu, Saffet4; Soon, Su-Tzai4; Cuong Tran4; Fairley, David4; Kleeman, Michael J.1
2019-12-05
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2019
卷号19期号:23页码:14677-14702
文章类型Article
语种英语
国家USA; Peoples R China
英文摘要

Regional concentrations and source contributions are calculated for airborne particle number concentration (N-x) and ultrafine particle mass concentration (PM0.1) in the San Francisco Bay Area (SFBA) and the South Coast Air Basin (SoCAB) surrounding Los Angeles with 4 km spatial resolution and daily time resolution for selected months in the years 2012, 2015, and 2016. Performance statistics for daily predictions of N-10 concentrations meet the goals typically used for modeling of PM2.5 (mean fractional bias (MFB) < +/- 0.5 and mean fractional error (MFE) < 0.75). The relative ranking and concentration range of source contributions to PM0.1 predicted by regional calculations agree with results from receptor-based studies that use molecular markers for source apportionment at four locations in California. Different sources dominated regional concentrations of N-10 and PM0.1 because of the different emitted particle size distributions and different choices for heating fuels. Nucleation (24%-57%) made the largest single contribution to N-10 concentrations at the 10 regional monitoring locations, followed by natural gas combustion (28%-45%), aircraft (2%-10%), mobile sources (1%-5%), food cooking (1%-2%), and wood smoke (0%-1%). In contrast, natural gas combustion (22%-52%) was the largest source of PM0.1 followed by mobile sources (15%-42%), food cooking (4%-14%), wood combustion (1%-12%), and aircraft (2%-6%). The study region encompassed in this project is home to more than 25 million residents, which should provide sufficient power for future epidemiological studies on the health effects of airborne ultrafine particles. All of the PM0.1 and N-10 outdoor exposure fields produced in the current study are available free of charge at http://webwolf.engr.ucdavis.edu/data/soa_v3/hourly_avg/ (last access: 20 November 2019).


领域地球科学
收录类别SCI-E
WOS记录号WOS:000501517100001
WOS关键词AIR-POLLUTION SOURCES ; LONG-TERM EXPOSURE ; POSITIVE MATRIX FACTORIZATION ; PARTICULATE MATTER EMISSIONS ; SAN-JOAQUIN VALLEY ; SOURCE APPORTIONMENT ; ORGANIC-COMPOUNDS ; SIZE DISTRIBUTION ; QUALITY MODEL ; COMPOSITION DISTRIBUTIONS
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/224105
专题环境与发展全球科技态势
作者单位1.Univ Calif Davis, Dept Civil & Environm Engn, One Shields Ave, Davis, CA 95616 USA;
2.Univ Calif Davis, Dept Land Air & Water Resources, One Shields Ave, Davis, CA 95616 USA;
3.Nanjing Univ Informat Sci & Technol, Sch Environm Sci & Engn, Nanjing, Jiangsu, Peoples R China;
4.Bay Area Air Qual Management Dist, San Francisco, CA USA
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Yu, Xin,Venecek, Melissa,Kumar, Anikender,et al. Regional sources of airborne ultrafine particle number and mass concentrations in California[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2019,19(23):14677-14702.
APA Yu, Xin.,Venecek, Melissa.,Kumar, Anikender.,Hu, Jianlin.,Tanrikulu, Saffet.,...&Kleeman, Michael J..(2019).Regional sources of airborne ultrafine particle number and mass concentrations in California.ATMOSPHERIC CHEMISTRY AND PHYSICS,19(23),14677-14702.
MLA Yu, Xin,et al."Regional sources of airborne ultrafine particle number and mass concentrations in California".ATMOSPHERIC CHEMISTRY AND PHYSICS 19.23(2019):14677-14702.
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