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Indoor air pollution has been recognized as an important risk factor for human health, especially in areas where people tend to spend most of their time indoors. Many semi-volatile organic compounds (SVOCs) have primarily indoor sources and are present in orders of magnitude higher concentrations indoors than outdoors. Despite this, awareness of SVOCs in indoor air and assessment of the link between indoor concentrations and human health have tagged behind those of outdoor air. This is partially related to challenges associated with indoor sampling of SVOCs. Passive air samplers (PASs), which are widely accepted in established outdoor air monitoring networks, have been used to fill the knowledge gaps on indoor SVOCs distribution. However, their applicability for indoor environments and the assessment of human health risks lack sufficient experimental data. To address this issue, we performed an indoor calibration study of polyurethane foam (PUF) PAS deployed in a double-dome chamber, covering both legacy and new SVOC classes. PUF-PAS and a continuous low-volume active air sampler (AAS) were co-deployed for a calibration period of twelve weeks. Based on the results from this evaluation, PUF-PAS in a double-bowl chamber is recommended for indoor sampling and health risk assessment of gas phase SVOCs, including novel brominated flame retardants (nBFR) providing sufficient exposure time is applied. Data for particle associated SVOCs suffered from significant uncertainties caused by low level of detection and low precision in this study. A more open chamber design for indoor studies may allow for higher sampling rates (R-s) and better performance for the particle associated SVOCs.

Polyurethane foam (PUF) disk passive air samplers were deployed concurrently at five sites across Kolkata megacity and the rural mangrove wetland of Sundarban (UNESCO World Heritage Site) between January-March in 2014. Samples were analyzed for hexachlorocyclohexanes (HCHs), dichlorodiphenyltricholoroethanes (DDTs), polychlorinated biphenyls (PCBs) and, polybrominated diphenyl ethers (PBDEs) using gas chromatography and mass spectrometry (GC-MS). Derived air concentrations (pg/m(3)) for Kolkata ranged: for Sigma alpha- and gamma-HCH between 70 and 207 (114 +/- 62), Sigma 6DDTs: 127-216 (161 +/- 36), Sigma(7)PCBs: 53-213 (141 +/- 64), and Sigma 10PBDEs: 0.30-23 (11 +/- 9). Low values for all the studied POPs were recorded in the remote area of the Sundarban site (with the exception of DDTs: o,p'-DDT and p,p'-DDT), where Sigma 4DDTs was 161 +/- 36. In particular, the site of Ballygunge, located in the southern part of Kolkata, showed the highest level of all the metabolites/congeners of POPs, suggesting a potential hot spot of usage and emissions. From HCHs, alpha-/gamma-HCH isomers ratio was low (0.67-1.96) indicating a possible sporadic source of lindane. y-HCH dominated the HCH signal (at 3 sites) reflecting wide spread use of lindane both in Kolkata and the Sundarban region; however, isomeric composition in Kolkata also suggests potential technical HCHs use. Among DDT metabolites, both o,p'-DDT and p,p'-DDT shared the dominant percentages accounting for 26-46% of total DDTs followed by p,p'-DDE (similar to 12-19%). The PCB congener profile was dominated by tri- and tetra-CI at the southern and eastern part of Kolkata. These results are one of the few contributions that reports air concentrations of POPs, concurrently, at urban and remote villages in India. These data are useful to assess atmospheric pollution levels and to motivate local and regional authorities to better understand the potential human exposure risk associated to urban areas in India.

PCBs and PBDEs (7 and 10 congeners, respectively) were analyzed in four coastal surface sediments collected from the northern shore of Bahia Blanca estuary and in nine soils from different locations of Bahia Blanca city and the surrounding region (Southwest of Buenos Aires Province, Argentina). Sediment samples showed PCBs((Sigma 7)) concentrations ranged from 0.61 to 17.6 ng g(-1) (dry weight = dw) and PBDEs(Sigma 10) from 0.16 to 2.02 ng g(-1) dw, whereas in soil samples ranged from 0.04 to 1.67 ng g(-1) dw for PCBs((Sigma 7)) and 0.04 to 10.7 ng g(-1) dw for PBDEs(Sigma 10). The highest concentrations of both chemicals were detected in the urban and industrial/port areas showing a dominance of the higher chlorinated PCB congeners: in sediments for PCB-180 (56 +/- 33%) and PCB-153 (11 +/- 6%); and in soils for PCB-138 (23 +/- 3%), PCB-153 (22 +/- 2%) and PCB-180 (18 +/- 7%). In contrast, lower chlorinated PCB congeners were predominant at more distant sites; in sediments for congeners PCB-28 (33 +/- 4%) and PCB-52 (14.5 +/- 0.2%); and in soils PCB-28 (56 +/- 14%) and PCB-52 (33 +/- 19%). PBDE-209 (high brominated PBDE) showed the highest relative abundance in both sample types i.e., sediment (94 +/- 7%) and soil (80 +/- 12%). These findings can be considered lower or similar when compared with other sites of the world, and are likely associated with anthropogenic activities in their surrounding area, which has experienced a fast industrial growth in the last decade. This is the first investigation of PBDEs levels in the whole study area and of PCBs in soils from the Bahia Blanca city and surrounding region. This article provides new and useful information on POP levels in the South eastern part of the GRULAC region.

Concentrations of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), and polybrominated diphenyl ethers (PBDEs) in air and soil, their fugacities, and the experimental soil-air partitioning coefficient (KSA) were determined at two background sites in the Gt. Hungarian Plain in August 2013. The concentrations of the semivolatile organic compounds (SOCs) in the soil were not correlated with the organic carbon content but with two indirect parameters of mineralization and aromaticity, suggesting that soil organic matter quality is an important parameter affecting the sorption of SOCs onto soils. Predictions based on the assumption that absorption is the dominant process were in good agreement with the measurements for PAHs, OCPs, and the low chlorinated PCBs. In general, soils were found to be a source of PAHs, high chlorinated PCBs, the majority of OCPs and PBDEs, and a sink for the low chlorinated PCBs and γ-hexachlorocyclohexane. Diurnal variations in the direction of the soil-air exchange were found for two compounds (i.e., pentachlorobenzene and p,p'-dichlorodiphenyldichloroethane), with volatilization during the day and deposition in the night. The concentrations of most SOCs in the near-ground atmosphere were dominated by revolatilization from the soil.

As a consequence of long-range transported pollution air-sea exchange can become a major source of persistent organic pollutants in remote marine environments. The vertical gradients in air of 14 species i.e., 4 parent polycyclic aromatic hydrocarbons (PAHs), 3 polychlorinated biphenyls (PCBs), 3 organochlorine pesticides (OCPs) and 2 polybrominated diphenylethers (PBDEs) in the gas-phase were quantified at a remote coastal site in the southern Aegean Sea in summer. Most vertical gradients were positive (Δc/Δz > 0) indicating downward (net depositional) flux. Significant upward (net volatilisational) fluxes were found for 3 PAHs, mostly during day-time, and for 2 OCPs, mostly during night-time, as well as for 1 PCB and 1 PBDE during part of the measurements. While phenanthrene was deposited, fluoranthene (FLT) and pyrene (PYR) seem to undergo flux oscillation, hereby not following a day/night cycle. Box modelling confirms that volatilisation from the sea surface has significantly contributed to the night-time maxima of OCPs. Fluxes were quantified based on Eddy covariance. Deposition fluxes ranged −28.5 − +1.8 μg m−2 d−1 for PAHs and −3.4 − +0.9 μg m−2 d−1 for halogenated compounds. Dry particle deposition of FLT and PYR did not contribute significantly to the vertical flux.

Near-ground air (26 substances) and surface seawater (55 substances) concentrations of persistent toxic substances (PTS) were determined in July 2012 in a coordinated and coherent way around the Aegean Sea based on passive air (10 sites in 5 areas) and water (4 sites in 2 areas) sampling. The direction of air–sea exchange was determined for 18 PTS. Identical samplers were deployed at all sites and were analysed at one laboratory. hexachlorobenzene (HCB), hexachlorocyclohexanes (HCHs) as well as dichlorodiphenyltrichloroethane (DDT) and its degradation products are evenly distributed in the air of the whole region. Air concentrations of p,p′-dichlorodiphenyldichloroethylene (p,p′-DDE) and o,p′-DDT and seawater concentrations of p,p′-DDE and p,p′-DDD were elevated in Thermaikos Gulf, northwestern Aegean Sea. The polychlorinated biphenyl (PCB) congener pattern in air is identical throughout the region, while polybrominated diphenylether (PBDE)patterns are obviously dissimilar between Greece and Turkey. Various pollutants, polycyclic aromatic hydrocarbons (PAHs), PCBs, DDE, and penta- and hexachlorobenzene are found close to phase equilibrium or net-volatilisational (upward flux), similarly at a remote site (on Crete) and in the more polluted Thermaikos Gulf. The results suggest that effective passive air sampling volumes may not be representative across sites when PAHs significantly partitioning to the particulate phase are included., Granting Agency of the Czech Republic (312334); Czech Ministry of Education (LO1214--LM2011028); European Social Fund (CZ.1.07/2.3.00/30.0037); European Commission FP7 (262254 ACTRIS)

Melting glaciers are natural redistributors of legacy airborne pollutants, affecting exposure of pristine proglacial environments. Our data shows that melting Himalayan glaciers can be major contributors of polychlorinated biphenyls (PCBs) and high-molecular-weight polycyclic aromatic hydrocarbons (PAHs) for surface water in the Gangetic Plain during the dry season. Glacial emissions can exceed in some cases inputs from diffuse sources within the catchment. We analyzed air, deposition and river water in several sections along the Ganges River and its major headwaters. The predominant glacial origin of these contaminants in the Himalayan reach was demonstrated using air-water fugacity ratios and mass balance analysis. The proportion of meltwater emissions compared to pollutant discharge at downstream sections in the central part of the Gangetic Plain was between 2 and 200%. By remobilizing legacy pollutants from melting glaciers, climate change can enhance exposure levels over large and already heavily impacted regions of Northern India.

Wide distribution of chlorinated paraffins in the environment has already been demonstrated in several studies; however, information about their levels in the Central Europe is still very limited. First study focused on the SCCP contamination of the Czech aquatic environment have been performed recently, and its results motivated the authors to analyze sediments from a wide set of the Czech rivers in order to obtain more detailed information. Thirty-six sediment samples from eleven rivers and five drainage vents neighboring the chemical factories were analyzed; special attention was paid to the industrial areas. For the first time in the Czech Republic, medium-chain in addition to short-chain chlorinated paraffins were analyzed using GC-ECNI-MS. Chlorinated paraffins were detected in sediment samples on the concentration levels up to 347 ngg(-1) for short-chain chlorinated paraffins, and 5575 ngg(-1) for medium-chain chlorinated paraffins. Average chlorination degree of SCCPs was 65%.

The most commonly used passive air sampler (PAS) (i.e. polyurethane foam (PUF) disk) is cheap, versatile, and capable of accumulating compounds present both in gas and particle phases. Its performance for particle associated compounds is however disputable. In this study, twelve sets of triplicate PUF-PAS were deployed outdoors for exposure periods of 1–12 weeks together with continuously operated active samplers, to characterize sampling efficiency and derive sampling rates (RS) for compounds belonging to 7 SVOC classes (including particle associated compounds). PUF-PAS efficiently and consistently sampled polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs), and eight novel brominated flame retardant (nBFR) compounds. Low accuracy and lack of sensitivity was observed for most polychlorinated dibenzo-p-dioxins/furans PCDD/Fs and polybrominated diphenyl ethers (PBDEs) (under the conditions of this study), with the exception of some congeners which may be used as qualitative markers for their respective classes. Application of compound specific RS was found crucial for all compounds except PCBs. Sampling efficiency of the particle associated compounds was often low.

A 6-month air sampling survey was conducted at 26 sites across the African continent with the aim to establish baseline information on contamination of ambient air with persistent organic pollutants (POPs) as a reference for future monitoring programs in the region. Sampling sites included continental, rural and urban backgrounds, agricultural and industrial sites as well as waste and obsolete pesticide dumps. Concentrations of polycyclic aromatic hydrocarbons, polychlorinated dibenzo-p-dioxins and furans, polychlorinated biphenyls and organochlorine pesticides were low at most of the rural background sites, but they raise some concern in big cities. The large temporal variability in the pesticide concentrations suggested seasonal application of gamma-HCHs and endosulfans; levels of p,p'-DDT were often much higher than those of p,p'-DDE and indicated recent application of DDT.

Central and Eastern Europe is a region that is expected to need more data on the concentrations of persistent organic pollutants (POPs) in the ambient air in the future. Passive air sampling is a cheap screening method for comparison of contamination on various sites or for verification of information obtained by active samplers. Passive air samplers are sensitive enough to mirror even small-scale differences, which makes them capable of monitoring spatial, seasonal, and temporal variations. Different passive air samplers were employed between 1990 and 2013 from time to time in six Estonian air monitoring stations. The concentrations of PCB and its congeners, HCB, PeCB, HCH, and DDT (the same for PBDE, PCN, PCDD/F) in Estonian ambient air were very low, but they allow tracking transboundary air pollution. The main aim of this article is analysis of changes in the ambient air pollution in Estonia during a long period of time (1990-2013). Also, selection of Lahemaa background station for monitoring POPs in the European area is addressed.