Trans-Pacific and regional atmospheric transport of polycyclic aromatic hydrocarbons and pesticides in biomass burning emissions to western North America.

The trans-Pacific and regional North American atmospheric transport of polycyclic aromatic hydrocarbons (PAHs) and pesticides in biomass burning emissions was measured in air masses from April to September 2003 at two remote sites in western North America. Mary's Peak Observatory (MPO) is located in Oregon's Coast Range and Cheeka Peak Observatory (CPO) is located on the tip of the Olympic Peninsula in Washington State. During this time period, both remote sites were influenced by PAH and pesticide emissions from forest fires in Siberia and regional fires in Oregon and Washington State.

Influence of Asian and Western United states agricultural areas and fires on the atmospheric transport of pesticides in the Western United States.

Historic and current use pesticides (HUPs and CUPs), with respect to use in the United States and Canada, were identified in trans-Pacific and regional air masses at Mt. Bachelor Observatory (MBO), a remote high elevation mountain in Oregon's Cascade Range located in the United States, during the sampling period of April 2004 to May 2006 (n = 69), including NASA's INTEX-B campaign (spring 2006). Elevated hexachlorobenzene (HCB) and alpha-hexachlorocyclohexane (alpha-HCH) concentrations were measured during trans-Pacific atmospheric transport events at MBO, suggesting that Asia is an important source region for these HUPs.

Influence of Asian and Western United States urban areas and fires on the atmospheric transport of polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and fluorotelomer alcohols in the Western United States.

Atmospheric measurements of semivolatile organic compounds (SOCs) were made at Mt Bachelor Observatory (MBO), located in Oregon's Cascade Range, to understand the trans-Pacific and regional transport of SOCs from urban areas. High volume air sampling (approximately 644 m3 for 24 h periods) of both the gas and particulate phases was conducted from April 19, 2004 to May 13, 2006 (n = 69); including NASA's INTEX-B campaign in spring 2006 (n = 34 of 69). Air mass back trajectories were calculated and were used to calculate source region impact factors (SRIFs), the percentage of time the sampled air mass resided in a given source region.

Atmospheric outflow of anthropogenic semivolatile organic compounds from East Asia in spring 2004.

To estimate the emissions of anthropogenic semivolatile organic compounds (SOCs) from East Asia and to identify unique SOC molecular markers in Asian air masses, high-volume air samples were collected on the island of Okinawa, Japan between 22 March and 2 May 2004. Contributions from different source regions (China, Japan, the Koreas, Russia, and ocean/local) were estimated by use of source region impact factors (SRIFs). Elevated concentrations of hexachlorobenzene (HCB), hexachlorcyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs), and particulate-phase polycyclic aromatic hydrocarbons (PAHs) were attributed to air masses from China.

Improved prediction of octanol-water partition coefficients from liquid-solute water solubilities and molar volumes.

A volume-fraction-based solvent-water partition model for dilute solutes, in which the partition coefficient shows a dependence on solute molar volume (V), is adapted to predict the octanol-water partition coefficient (K(ow)) from the liquid or supercooled-liquid solute water solubility (Sw), or vice versa. The established correlation is tested for a wide range of industrial compounds and pesticides (e.g.