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Contributions of local pollution emissions to particle bioreactivity in downwind cities in China during Asian dust periods

Research output: Contribution to journalArticlepeer-review

Abstract

This study investigated the effects of pollution emissions on the bioreactivity of PM 2.5 during Asian dust periods. PM 2.5 during the sampling period were 104.2 and 85.7 μg m −3 in Xi'an and Beijing, respectively, whereas PM 2.5 which originated from the Tengger Desert was collected (dust background). Pollution conditions were classified as non-dust days, pollution episode (PE), dust storm (DS)-1, and DS-2 periods. We observed a significant decrease in cell viability and an increase in LDH that occurred in A549 cells after exposure to PM 2.5 during a PE and DS-1 in Xi'an and Beijing compared to Tengger Desert PM 2.5 . Positive matrix factorization was used to identify pollution emission sources. PM 2.5 from biomass and industrial sources contributed to alterations in cell viability and LDH in Xi'an, whereas vehicle emissions contributed to LDH in Beijing. OC, EC, Cl , K + , Mg 2+ , Ca, Ti, Mn, Fe, Zn, and Pb were correlated with cell viability and LDH for industrial emissions in Xi'an during DS. OC, EC, SO 4 2− , S, Ti, Mn, and Fe were correlated with LDH for vehicle emissions in Beijing during DS. In conclusion, the dust may carry pollutants on its surface to downwind areas, leading to increased risks of particle toxicity.

Original languageEnglish
Pages (from-to)675-683
Number of pages9
JournalEnvironmental Pollution
Volume245
DOIs
Publication statusPublished - Feb 1 2019

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 11 - Sustainable Cities and Communities
    SDG 11 Sustainable Cities and Communities

Keywords

  • Air pollution
  • Dust storm
  • Metal
  • Physicochemistry
  • Source apportionment

ASJC Scopus subject areas

  • Toxicology
  • Pollution
  • Health, Toxicology and Mutagenesis

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