PM10-bound trace elements in the Great Lakes Basin (1988–2017) indicates effectiveness of regulatory actions, variations in sources and reduction in human health risks. (October 2020)

• Record Type: Journal Article
• Authors: Li, Wenlong; Dryfhout-Clark, Helena; Hung, Hayley
• Is Part Of: Environment international. Volume 143(2020)
• Publication Date: 2020-10
• Subjects: Health risk -- Trace elements -- The Great Lakes -- Temporal trends -- Source apportionment; Environmental protection -- Periodicals; Environmental health -- Periodicals; Environmental monitoring -- Periodicals; Environmental Monitoring -- Periodicals; Environnement -- Protection -- Périodiques; Hygiène du milieu -- Périodiques; Environnement -- Surveillance -- Périodiques; Environmental health; Environmental monitoring; Environmental protection; Periodicals; 333.705
• DOI: 10.1016/j.envint.2020.106008
• Languages: English
• ISSNs: 0160-4120

Abstract

Graphical abstract: Highlights: Spatial distributions of trace elements correspond to local population distributions. Most target elements in the Great Lakes atmosphere significantly decreased over time. Most atmospheric trace elements were from anthropogenic sources. Studied elements mostly originated from the United States. Potential cancer risk posed by inhalation of some elements exceeded the USEPA acceptable levels. Abstract: Limited studies focus on the effectiveness of regulatory actions on changes in sources and temporal trends of human health risks for trace elements in atmospheric particles < 10 μm (PM10 ). To address this knowledge gap, PM10 samples were collected at three stations in the Great Lakes Basin over a thirty-year time span and analyzed for 19 representative elements. Temporal trends of trace elements in PM10 were derived using the Digital Filtration Technique and sources of these elements were determined using multiple statistical techniques, namely enrichment factor analysis, positive matrix factorization (PMF) and potential source contribution function (PSCF). Non-carcinogenic and carcinogenic risks by chronic exposure were assessed using US EPA reference concentrations and inhalation unit risk. Our results showed a strong relationship between element concentrations and local populations, which suggested that the emissions of trace elements were anthropogenically-related and was confirmed by the enrichment factor analysis. The concentrations of most elements were significantly decreasing with halving times ranging from 10 to 48 years in response to national and international regulatory actions. Specific origins of atmospheric trace elements were from the copper refining industry, refuse incineration, coal combustion, vehicle emissions, oil/coal-fired power plants, and crustal/soil dust. Potential source region analysis indicates dominant sources south of the sampling sites in the US, associated with a higher population and more industrial and transportation activities. The possibility of non-cancer health effects due to inhalation were mostly within acceptable levels. However, potential cancer risk posed by inhalation of some elements cannot be ignored, with values approaching or higher than the acceptable level. Considering that the sampling locations are remote and regionally-representative, our finding emphasizes the importance of continued monitoring of metals in air to assess the effectiveness of control strategies.