Abstract
This study examines co-located aerosol and precipitation chemistry data between 2010 and 2016 at Pinnacles National Monument ~65 km east of the coastline in central California. Positive matrix factorization analysis of the aerosol composition data revealed seven distinct pollutant sources: aged sea salt (25.7% of PM2.5), biomass burning (24.2% of PM2.5), fresh sea salt (15.0% of PM2.5), secondary sulfate (11.7% of PM2.5), dust (10.0% of PM2.5), vehicle emissions (8.2% of PM2.5), and secondary nitrate (5.2% of PM2.5). The influence of meteorology and transport on monthly patterns of PM2.5 composition is discussed. Only secondary sulfate exhibited a statistically significant change (a reduction) over time among the PM2.5 source factors. In contrast, PMcoarse exhibited a significant increase most likely due to dust influence. Monthly profiles of precipitation chemistry are summarized showing that the most abundant species in each month was either SO4 2−, NO3 −, or Cl−. Intercomparisons between the precipitation and aerosol data revealed several features: (i) precipitation pH was inversely related to factors associated with more acidic aerosol constituents such as secondary sulfate and aged sea salt, in addition to being reduced by uptake of HNO3 in the liquid phase; (ii) two aerosol source factors (dust and aged sea salt) and PMcoarse exhibited a positive association with Ca2+ in precipitation, suggestive of directly emitted aerosol types with larger sizes promoting precipitation; and (iii) sulfate levels in both the aerosol and precipitation samples analyzed were significantly correlated with dust and aged sea salt PMF factors, pointing to the partitioning of secondary sulfate to dust and sea salt particles. The results of this work have implications for the region's air quality and hydrological cycle, in addition to demonstrating that the use of co-located aerosol and precipitation chemistry data can provide insights relevant to aerosol-precipitation interactions.
| Language | English (US) |
|---|---|
| Pages | 1776-1787 |
| Number of pages | 12 |
| Journal | Science of the Total Environment |
| Volume | 651 |
| DOIs | |
| State | Published - Feb 15 2019 |
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Keywords
- Biomass burning
- IMPROVE
- NADP
- Pinnacles National Monument
- PMF
- Sea salt
ASJC Scopus subject areas
- Environmental Engineering
- Environmental Chemistry
- Waste Management and Disposal
- Pollution
Cite this
Sources of pollution and interrelationships between aerosol and precipitation chemistry at a central California site. / Dadashazar, Hossein; Ma, Lin; Sorooshian, Armin.
In: Science of the Total Environment, Vol. 651, 15.02.2019, p. 1776-1787.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Sources of pollution and interrelationships between aerosol and precipitation chemistry at a central California site
AU - Dadashazar, Hossein
AU - Ma, Lin
AU - Sorooshian, Armin
PY - 2019/2/15
Y1 - 2019/2/15
N2 - This study examines co-located aerosol and precipitation chemistry data between 2010 and 2016 at Pinnacles National Monument ~65 km east of the coastline in central California. Positive matrix factorization analysis of the aerosol composition data revealed seven distinct pollutant sources: aged sea salt (25.7% of PM2.5), biomass burning (24.2% of PM2.5), fresh sea salt (15.0% of PM2.5), secondary sulfate (11.7% of PM2.5), dust (10.0% of PM2.5), vehicle emissions (8.2% of PM2.5), and secondary nitrate (5.2% of PM2.5). The influence of meteorology and transport on monthly patterns of PM2.5 composition is discussed. Only secondary sulfate exhibited a statistically significant change (a reduction) over time among the PM2.5 source factors. In contrast, PMcoarse exhibited a significant increase most likely due to dust influence. Monthly profiles of precipitation chemistry are summarized showing that the most abundant species in each month was either SO4 2−, NO3 −, or Cl−. Intercomparisons between the precipitation and aerosol data revealed several features: (i) precipitation pH was inversely related to factors associated with more acidic aerosol constituents such as secondary sulfate and aged sea salt, in addition to being reduced by uptake of HNO3 in the liquid phase; (ii) two aerosol source factors (dust and aged sea salt) and PMcoarse exhibited a positive association with Ca2+ in precipitation, suggestive of directly emitted aerosol types with larger sizes promoting precipitation; and (iii) sulfate levels in both the aerosol and precipitation samples analyzed were significantly correlated with dust and aged sea salt PMF factors, pointing to the partitioning of secondary sulfate to dust and sea salt particles. The results of this work have implications for the region's air quality and hydrological cycle, in addition to demonstrating that the use of co-located aerosol and precipitation chemistry data can provide insights relevant to aerosol-precipitation interactions.
AB - This study examines co-located aerosol and precipitation chemistry data between 2010 and 2016 at Pinnacles National Monument ~65 km east of the coastline in central California. Positive matrix factorization analysis of the aerosol composition data revealed seven distinct pollutant sources: aged sea salt (25.7% of PM2.5), biomass burning (24.2% of PM2.5), fresh sea salt (15.0% of PM2.5), secondary sulfate (11.7% of PM2.5), dust (10.0% of PM2.5), vehicle emissions (8.2% of PM2.5), and secondary nitrate (5.2% of PM2.5). The influence of meteorology and transport on monthly patterns of PM2.5 composition is discussed. Only secondary sulfate exhibited a statistically significant change (a reduction) over time among the PM2.5 source factors. In contrast, PMcoarse exhibited a significant increase most likely due to dust influence. Monthly profiles of precipitation chemistry are summarized showing that the most abundant species in each month was either SO4 2−, NO3 −, or Cl−. Intercomparisons between the precipitation and aerosol data revealed several features: (i) precipitation pH was inversely related to factors associated with more acidic aerosol constituents such as secondary sulfate and aged sea salt, in addition to being reduced by uptake of HNO3 in the liquid phase; (ii) two aerosol source factors (dust and aged sea salt) and PMcoarse exhibited a positive association with Ca2+ in precipitation, suggestive of directly emitted aerosol types with larger sizes promoting precipitation; and (iii) sulfate levels in both the aerosol and precipitation samples analyzed were significantly correlated with dust and aged sea salt PMF factors, pointing to the partitioning of secondary sulfate to dust and sea salt particles. The results of this work have implications for the region's air quality and hydrological cycle, in addition to demonstrating that the use of co-located aerosol and precipitation chemistry data can provide insights relevant to aerosol-precipitation interactions.
KW - Biomass burning
KW - IMPROVE
KW - NADP
KW - Pinnacles National Monument
KW - PMF
KW - Sea salt
UR - http://www.scopus.com/inward/record.url?scp=85054451741&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85054451741&partnerID=8YFLogxK
U2 - 10.1016/j.scitotenv.2018.10.086
DO - 10.1016/j.scitotenv.2018.10.086
M3 - Article
VL - 651
SP - 1776
EP - 1787
JO - Science of the Total Environment
T2 - Science of the Total Environment
JF - Science of the Total Environment
SN - 0048-9697
ER -