Eric S. Coker, Aline Maybank, Young Jae Lim, Liddy Boland, Inumidun Oyebode, Elizabeth Z. Lin, Jieqiong Zhou, Scott Weichenthal, Krystal J. Godri Pollitt
{"title":"Wildfire Smoke beyond PM2.5: Distinct Chemical Mixtures and Hazard Profiles","authors":"Eric S. Coker, Aline Maybank, Young Jae Lim, Liddy Boland, Inumidun Oyebode, Elizabeth Z. Lin, Jieqiong Zhou, Scott Weichenthal, Krystal J. Godri Pollitt","doi":"10.1021/acsestair.6c00092","DOIUrl":null,"url":null,"abstract":"<p>Despite growing concern\r\nabout wildfire smoke (WFS) exposure, research\r\nhas largely focused on fine particle (PM<sub>2.5</sub>) mass rather\r\nthan the complex airborne chemical mixtures that may pose distinct\r\nhealth risks. From March to September 2024, passive air samplers in\r\ntwo British Columbia communities collected chemical profiles before,\r\nduring, and after WFS episodes. Gas chromatography high-resolution\r\nmass spectrometry (GC-HRMS) characterized WFS using targeted and nontargeted\r\napproaches. Targeted analysis quantified the concentrations of 35\r\nvolatile and semivolatile organic compounds (VOCs/SVOCs), while nontargeted\r\nanalysis (NTA) detected 294 chemicals. Cluster analysis of targeted\r\ncompounds identified four chemical profiles: two representing site-specific\r\nurban background compounds and two enriched with combustion byproducts,\r\nincluding polycyclic aromatic hydrocarbons (PAHs), during episodic\r\nWFS. Hierarchical clustering of the NTA chemicals identified mixtures\r\ncorresponding to distinct hazard profiles of regionally and locally\r\ntransported WFS from urban background chemical mixtures. Chemical\r\nmixtures of regionally transported and locally transported smoke exhibited\r\nenrichment patterns of compounds with known developmental, endocrine-disruption,\r\nand mutagenic-genotoxic hazards. These findings demonstrate that WFS\r\nforms complex, yet reproducible, multipollutant mixtures beyond PM<sub>2.5</sub> and emphasize the need to evaluate long-term chemical exposures\r\nand their potential contribution to chronic health risks.</p>","PeriodicalId":100014,"journal":{"name":"ACS ES&T Air","volume":"3 9","pages":"2254–2269"},"PeriodicalIF":0.0000,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS ES&T Air","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsestair.6c00092","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/10 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Despite growing concern
about wildfire smoke (WFS) exposure, research
has largely focused on fine particle (PM2.5) mass rather
than the complex airborne chemical mixtures that may pose distinct
health risks. From March to September 2024, passive air samplers in
two British Columbia communities collected chemical profiles before,
during, and after WFS episodes. Gas chromatography high-resolution
mass spectrometry (GC-HRMS) characterized WFS using targeted and nontargeted
approaches. Targeted analysis quantified the concentrations of 35
volatile and semivolatile organic compounds (VOCs/SVOCs), while nontargeted
analysis (NTA) detected 294 chemicals. Cluster analysis of targeted
compounds identified four chemical profiles: two representing site-specific
urban background compounds and two enriched with combustion byproducts,
including polycyclic aromatic hydrocarbons (PAHs), during episodic
WFS. Hierarchical clustering of the NTA chemicals identified mixtures
corresponding to distinct hazard profiles of regionally and locally
transported WFS from urban background chemical mixtures. Chemical
mixtures of regionally transported and locally transported smoke exhibited
enrichment patterns of compounds with known developmental, endocrine-disruption,
and mutagenic-genotoxic hazards. These findings demonstrate that WFS
forms complex, yet reproducible, multipollutant mixtures beyond PM2.5 and emphasize the need to evaluate long-term chemical exposures
and their potential contribution to chronic health risks.