Concentrations, Trends, and Air–Water Exchange of PCBs and Organochlorine Pesticides Derived from Passive Samplers in Lake Superior in 2011

The largest fresh water body in North America, Lake Superior, has the potential to both accumulate and serve as a secondary source of persistent bioaccumulative toxins, such as polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs). Polyethylene passive samplers (PEs) were thus simultaneously deployed at 19 sites in surface water and near surface atmosphere across Lake Superior to determine air and water concentrations and air–water gradients of 18 PCBs and 24 OCPs. PCBs in the air and water were characterized by penta- and hexachlorobiphenyls with distribution along the coast correlated with proximity to developed areas. Surface water and atmospheric concentrations were dominated by α-HCH (average 250 pg L–1 and 4.2 pg m–3, respectively), followed by HCB (average 17 pg L–1 and 89 pg m–3, respectively). Decreases in open lake concentrations of PCBs in water and air from spring to summer were consistent with ongoing volatilization from the surface layer as the main cause. Conversely, α-endosulfan was consistently deposited into the surface water of Lake Superior. Results indicated that PCBs were depleted in the surface mixed layer, implying a physical limit on evasive fluxes. This was corroborated with measurements from a vertical profile, displaying greater PCB concentrations at depth

Concentrations, Trends, and Air-Water Exchange of PAHs and PBDEs Derived from Passive Samplers in Lake Superior in 2011

Polycyclic aromatic hydrocarbons (PAHs) and polybrominated diphenylethers (PBDEs) are both currently released into the environment from anthropogenic activity. Both are hence primarily associated with populated or industrial areas, although wildfires can be an important source of PAHs, too. Polyethylene passive samplers (PEs) were simultaneously deployed in surface water and near surface atmosphere to determine spatial trends and air-water gaseous exchange of 22 PAHs and 11 PBDEs at 19 sites across Lake Superior in 2011. Surface water and atmospheric PAH concentrations were greatest at urban sites (up to 65 ng L-1 and 140 ng m-3, respectively, averaged from June to October). Near populated regions, PAHs displayed net air-to-water deposition, but were near equilibrium off-shore. Retene, probably depositing following major wildfires in the region, dominated dissolved PAH concentrations at most Lake Superior sites. Atmospheric and dissolved PBDEs were greatest near urban and populated sites (up to 6.8 pg L-1 and 15 pg m-3, respectively, averaged from June to October), dominated by BDE-47. At most coastal sites, there was net gaseous deposition of BDE-47, with less brominated congeners contributing to Sault Ste. Marie and eastern open lake fluxes. Conversely, the central open lake and Eagle Harbor sites generally displayed volatilization of PBDEs into the atmosphere, mainly BDE-47