@proceedings {52841,
	title = {Measurement of polynuclear aromatic hydrocarbons (PAHs) in epiphytic lichens for receptor modeling in the Alberta oil sands region},
	year = {2013},
	note = {IN:  Harmonizing Science Across Disciplines.  SETAC North America 34th Annual Meeting November 17-21, 2013 Nashville Tennessee.  Paper $\#$ 474.  p. 115-116.},
	month = {11/2013},
	pages = {2 pages },
	address = {Nashville, TN},
	abstract = {As mining and refinery operations in the Alberta Oil Sands Region (AOSR) have expanded, there has been increasing concern for the impacts of air pollution generated by those operations on both human and ecosystem health. The inaccessibility of much of the AOSR makes it difficult to establish conventional air quality monitoring stations to the extent needed to model long-range impacts of emissions from the AOSR operations. Epiphytic lichens are important markers of ecosystem health, are well-established bioaccumulators of trace metals, and are potentially useful biomonitors of air pollution. However, their ability to take up organic pollutants has not been extensively explored, and only recently have they been used for biomonitoring of pollution by PAHs. Here we describe the determination of polynuclear aromatic hydrocarbons (PAHs) in lichens, collected from sites throughout the AOSR, for modeling emissions associated with mining and oil extraction operations. We also describe preliminary results of the determination of PAHs in PM 2.5 filters from dichotomous samplers stationed in the AOSR, in the context of the biological sample data. Lichens (Hypogymnia physodes) were collected on two separate occasions. During the summer of 2009, single samples were taken from 200 sites in the AOSR; a subset of 20 of these was selected for determination of PAHs. During the summer of 2011, triplicate samples (from separate trees within a site) were collected from 20 sites representing similar locations to the 2008 sites. Lichens were milled in a cryogenic impactor, then were extracted with cyclohexane. Extracts were purified on silica gel using automated solid phase extraction and analyzed by gas chromatography with mass selective detection. Method detection limits for individual PAHs were 2-4 ng/g. Total PAHs in the samples from both collection events ranged from 50 ng/g to 350 ng/g, and declined with increasing distance from the mining and refinery operations. The relative contribution of low ring number PAHs to total PAHs increased with increasing distance. Total PAHs correlated strongly (R2 > 0.80, p < 0.05) with crustal elements, suggesting similar transport mechanisms. Analytical data for PAHs on PM 2.5 filters, including relationships between concentrations, PAH profiles, and distance from the mines, will be presented. The lichen data are consistent with PAH transport close to the mines being more influenced by particulate matter transport mechanisms, whereas PAHs in samples collected from remote areas reflect more of the vapor phase transport mechanisms.},
	keywords = {air emissions, biomonitoring, hydrocarbon, lichen, PAH, VOC},
	author = {Studabaker, William and Krupa, S. and Jayanty, R. and Raymer, James}
}
