%0 Journal Article %J Environ Toxicol Chem %D 2017 %T Diffusive flux of PAHs across sediment-water and water-air interfaces at urban superfund sites. %A D James Minick %A Kim A Anderson %K Air %K Cities %K Geologic Sediments %K Hazardous Waste Sites %K Oregon %K Polycyclic Aromatic Hydrocarbons %K Rivers %K Water %K Water Pollutants, Chemical %X

Superfund sites may be a source of polycyclic aromatic hydrocarbons (PAHs) to the surrounding environment. These sites can also act as PAH sinks from present-day anthropogenic activities, especially in urban locations. Understanding PAH transport across environmental compartments helps to define the relative contributions of these sources and is therefore important for informing remedial and management decisions. In the present study, paired passive samplers were co-deployed at sediment-water and water-air interfaces within the Portland Harbor Superfund Site and the McCormick and Baxter Superfund Site. These sites, located along the Willamette River (Portland, OR, USA), have PAH contamination from both legacy and modern sources. Diffusive flux calculations indicate that the Willamette River acts predominantly as a sink for low molecular weight PAHs from both the sediment and the air. The sediment was also predominantly a source of 4- and 5-ring PAHs to the river, and the river was a source of these same PAHs to the air, indicating that legacy pollution may be contributing to PAH exposure for residents of the Portland urban center. At the remediated McCormick and Baxter Superfund Site, flux measurements highlight locations within the sand and rock sediment cap where contaminant breakthrough is occurring. Environ Toxicol Chem 2017;36:2281-2289. © 2017 SETAC.

%B Environ Toxicol Chem %V 36 %P 2281-2289 %8 2017 09 %G eng %N 9 %R 10.1002/etc.3785 %0 Journal Article %J J AOAC Int %D 2003 %T Determination of pyrethrin and pyrethroid pesticides in urine and water matrixes by liquid chromatography with diode array detection. %A Loper, Bobby R %A Kim A Anderson %K Calibration %K Chromatography, Liquid %K Humans %K Indicators and Reagents %K Insecticides %K Pyrethrins %K Reference Standards %K Spectrometry, Mass, Electrospray Ionization %K Spectrophotometry, Ultraviolet %K Water %X

The following pyrethrin and pyrethroid pesticides were determined in urine and water matrixes by liquid chromatography with diode array detection (LC-DAD): pyrethrin I, pyrethrin II, tetramethrin, baythroid, bifenthrin, fenvalerate, phenothrin, allethrin, resmethrin, cis-permethrin, and trans-permethrin. In addition, 3-phenoxybenzyl alcohol, a metabolite of various pyrethroids, was also successfully determined by the analytical method. The matrix extraction was simple, inexpensive, and fast, using only sodium chloride and acetonitrile. The acetonitrile extract was filtered and analyzed by LC-DAD. The method detection limits for the pyrethrin pesticides in 5 mL urine were determined to range from 0.002 to 0.04 microg/mL, depending on the individual pyrethrin. Recoveries from spiked tap water ranged from 77 to 96%; recoveries from urine ranged from 80 to 117%. This method is especially well-suited to clinical investigations, in which rapid analysis of forensic samples is often required.

%B J AOAC Int %V 86 %P 1236-40 %8 11/2003 %G eng %N 6 %1 http://www.ncbi.nlm.nih.gov/pubmed/14979708?dopt=Abstract