Using passive air samplers to assess local sources versus long range atmospheric transport of POPs.

Passive air samplers (PAS) are cost-efficient tools suitable for spatial mapping of atmospheric concentrations of persistent organic pollutants (POPs). The objective of this study was to use PAS to (i) determine atmospheric concentrations of selected POPs in Norwegian coastal zones with consumption advisories on seafood (N = 22), and (ii) evaluate a simple nested monitoring approach to assess the relative influence of local vs. long-range atmospheric transport (LRAT) at coastal sites. The latter was facilitated by comparison with data from a coordinated European-wide campaign in which an identical sampling and analytical approach was followed. Air concentrations were calculated based on the loss of performance reference compounds (PRCs), and results are presented for selected polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons (PAHs), hexachlorocyclohexanes (HCHs), hexachlorobenzene (HCB), dichlorodiphenyltrichloroethanes (DDTs) and chlordanes. Air concentrations of PCBs were generally highest at sites within larger cities and up to about an order of magnitude higher than anticipated on the basis of LRAT alone. The distribution of PAHs and HCB occasionally showed elevated concentrations at coastal sites with ongoing or former industrial activity, while an urban site was significantly influenced by banned insecticides (technical DDT and lindane). Coastal sites were also elevated in α-HCH beyond the anticipated LRAT contribution, which we attribute to volatilization from the sea. We conclude that a simple nested PAS monitoring approach provides useful information for screening efforts aiming to assess both atmospheric burdens as well as the relative significance of local sources in controlling these burdens at sites in contaminated areas.

Low concentrations of persistent organic pollutants (POPs) in air at Cape Verde.

Ambient air is a core medium for monitoring of persistent organic pollutants (POPs) under the Stockholm Convention and is used in studies of global transports of POPs and their atmospheric sources and source regions. Still, data based on active air sampling remain scarce in many regions. The primary objectives of this study were to (i) monitor concentrations of selected POPs in air outside West Africa, and (ii) to evaluate potential atmospheric processes and source regions affecting measured concentrations. For this purpose, an active high-volume air sampler was installed on the Cape Verde Atmospheric Observatory at Cape Verde outside the coast of West Africa. Sampling commenced in May 2012 and 43 samples (24h sampling) were collected until June 2013. The samples were analyzed for selected polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), hexachlorobenzene (HCB) and chlordanes. The concentrations of these POPs at Cape Verde were generally low and comparable to remote sites in the Arctic for several compounds. Seasonal trends varied between compounds and concentrations exhibited strong temperature dependence for chlordanes. Our results indicate net volatilization from the Atlantic Ocean north of Cape Verde as sources of these POPs. Air mass back trajectories demonstrated that air masses measured at Cape Verde were generally transported from the Atlantic Ocean or the North African continent. Overall, the low concentrations in air at Cape Verde were likely explained by absence of major emissions in areas from which the air masses originated combined with depletion during long-range atmospheric transport due to enhanced degradation under tropical conditions (high temperatures and concentrations of hydroxyl radicals).

Endosulfan, pentachlorobenzene and short-chain chlorinated paraffins in background soils from Western Europe.

Soils are major reservoirs for many persistent organic pollutants (POPs). In this study, "newly" regulated POPs i.e. Σendosulfans (α-endosulfan, ß-endosulfan, endosulfan sulfate), pentachlorobenzene (PeCB), and short-chain chlorinated paraffins (SCCPs) were determined in background samples from woodland (WL) and grassland (GL) surface soil, collected along an existing latitudinal UK-Norway transect. Statistical analysis, complemented with plots showing the predicted equilibrium distribution and mobility potential, was then explored to discuss factors controlling their spatial distribution. SCCPs were detected with the highest average concentrations (35 ± 100 ng/g soil organic matter (SOM)), followed by Σendosulfans (3 ± 3 ng/g SOM) and PeCB (1 ± 1 ng/g SOM). PeCB and Σendosulfans share many similarities in their distribution in these background soils as well as with several legacy POPs. A steep decline in concentrations of SCCPs with increasing latitude indicates that their occurrence is dictated by proximity to source regions, while concentrations of Σendosulfans peaked in regions experiencing elevated precipitation rates.