• LOGIN
Repository logo

BORIS Portal

Bern Open Repository and Information System

  • Publication
  • Projects
  • Funding
  • Research Data
  • Organizations
  • Researchers
  • LOGIN
Repository logo
Unibern.ch
  1. Home
  2. Publications
  3. Large contribution of fossil fuel derived secondary organic carbon to water soluble organic aerosols in winter haze in China
 

Large contribution of fossil fuel derived secondary organic carbon to water soluble organic aerosols in winter haze in China

Options
  • Details
BORIS DOI
10.7892/boris.113469
Date of Publication
2018
Publication Type
Article
Division/Institute

Departement für Chemi...

Author
Zhang, Yanlin
Departement für Chemie und Biochemie (DCB)
El-Haddad, Imad
Huang, Ru-Jin
Ho, Kin-Fai
Cao, Jun-Ji
Han, Yongming
Zotter, Peter
Bozzetti, Carlo
Daellenbach, Kaspar R.
Slowik, Jay G.
Salazar Quintero, Gary Abdiel
Departement für Chemie und Biochemie (DCB)
Prévôt, André S. H.
Szidat, Sönkeorcid-logo
Departement für Chemie und Biochemie (DCB)
Subject(s)

500 - Science::570 - ...

500 - Science::540 - ...

Series
Atmospheric chemistry and physics
ISSN or ISBN (if monograph)
1680-7316
Publisher
European Geosciences Union
Language
English
Publisher DOI
10.5194/acp-18-4005-2018
Description
Water-soluble organic carbon (WSOC) is a large fraction of organic aerosols (OA) globally and has significant impacts on climate and human health. The sources of WSOC remain very uncertain in polluted regions. Here we present a quantitative source apportionment of WSOC, isolated from aerosols in China using radiocarbon (14C) and offline high-resolution time-of-flight aerosol mass spectrometer measurements. Fossil emissions on average accounted for 32–47% of WSOC. Secondary organic carbon (SOC) dominated both the non-fossil and fossil derived WSOC, highlighting the importance of secondary formation to WSOC in severe winter haze episodes. Contributions from fossil emissions to SOC were 61±4 and 50±9% in Shanghai and Beijing, respectively, significantly larger than those in Guangzhou (36±9 %) and Xi’an (26±9 %). The most important primary sources were biomass burning emissions, contributing 17–26% of WSOC. The remaining primary sources such as coal combustion, cooking and traffic were generally very small but not negligible contributors, as coal combustion contribution could exceed 10 %. Taken together with earlier 14C source apportionment studies in urban, rural, semi-urban and background regions in Asia, Europe and the USA, we demonstrated a dominant contribution of non-fossil emissions (i.e., 75±11 %) to WSOC aerosols in the Northern Hemisphere; however, the fossil fraction is substantially larger in aerosols from East Asia and the eastern Asian pollution outflow, especially during winter, due to increasing coal combustion. Inclusion of our findings can improve a modelling of effects of WSOC aerosols on climate, atmospheric
chemistry and public health.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/159741
Show full item
File(s)
FileFile TypeFormatSizeLicensePublisher/Copright statementContent
Zhang_SOA source apportionment for China winter from 14C(WSOC) (ACP 2018).pdftextAdobe PDF1.92 MBAttribution (CC BY 4.0)publishedOpen
BORIS Portal
Bern Open Repository and Information System
Build: b407eb [23.05. 15:47]
Explore
  • Projects
  • Funding
  • Publications
  • Research Data
  • Organizations
  • Researchers
More
  • About BORIS Portal
  • Send Feedback
  • Cookie settings
  • Service Policy
Follow us on
  • Mastodon
  • YouTube
  • LinkedIn
UniBe logo