Anders Borgen

Dioxin-like chemicals in soil and sediment from residential and industrial areas in central South Africa.

Persistent organic pollutants (POPs) are a global concern due to their ubiquitous presence and toxicity. Currently, there is a lack of information regarding POPs from South Africa. Here we report and interpret concentrations of polychlorinated dibenzo-p-dioxins (PCDDs), -dibenzofurans (PCDFs) and co-planar-biphenyls (PCBs) in soils and sediments collected from central South Africa. High resolution gas chromatography-high resolution mass spectrometry (HRGC/HRMS) and the H4IIE-luc bio-assay were used to identify and quantify individual PCDD/F congeners and to report the total concentration of 2,3,7,8-tetrachloro dibenzo-p-dioxin equivalents (TCDD-EQ), respectively. TCDD-EQs determined by use of the bio-assay, and concentrations of WHO(2005)-TEQ (toxic equivalents) determined by chemical analysis, were similar. The limit of detection (LOD) for the bio-assay was 0.82 and 2.8 ng TCDD-EQ kg(-1), dw for sediment and soil, respectively. EQ20 concentrations determined by use of the bio-assay ranged from <LOD to 70 ng TCDD-EQ kg(-1), dw for soil, and from <LOD to 45 ng TCDD-EQ kg(-1), dw for sediment. Concentrations of WHO(2005)-TEQ in soils were generally greater than those in sediments, and soils from the industrial area of Vanderbijlpark and the residential area of Klerksdorp contained the greatest concentrations. Based on the congener-specific HRGC/HRMS analyzes, concentrations of WHO(2005)-TEQ ranged from 0.12 to 32 ng WHO(2005)-TEQ kg(-1), dw in sediments, and between 0.34 and 20 ng WHO(2005)-TEQkg(-1), dw in soils. The sources, processes and threats that govern and are associated with the lesser concentrations in sediment and greater concentrations in soils need further investigation.

Polycyclic Aromatic Hydrocarbons (PAHs) in Soil and Sediment from Industrial, Residential, and Agricultural Areas in Central South Africa: An Initial Assessment

Polycyclic aromatic hydrocarbons (PAHs) are of global concern due to their ubiquitous presence, toxicity, and carcinogenicity. No data on PAHs in soils from South Africa have been published, even though it has the largest economy and industrial base in Africa. During this initial assessment, the levels of PAHs were determined in soils and sediments collected from central South Africa, specifically targeting industrial, residential, and agricultural areas. Analysis was performed by gas chromatography/mass spectrometry (GC/MS). The total concentration of PAHs (Σt-PAH) ranged between 44 and 39,000 ng/g, dw and the concentration of carcinogenic PAHs (Σc-PAH) ranged between 19 and 19,000 ng/g, dw. Pyrogenic processes were the most likely sources, with minimal petrogenic contributions. PAH levels were in the same range as levels reported from other countries, and the majority of the sites did not exceed Canadian environmental quality guidelines. Based on assumptions for dermal contact and ingestion of PAH-contaminated soil, we provisionally calculated only a small increase in cancer risk, but additional PAH inhalation could add considerably to this risk. Our data indicates a need for more analysis in industrial and residential areas, and should include air.

Relevance of 1,2,5,6,9,10-hexabromocyclododecane diastereomer structure on partitioning properties, column-retention and clean-up procedures.

To optimize clean-up procedures for the analysis of alpha-, beta-, and gamma-hexabromocyclododecanes (HBCD) in environmental and biological extracts, their retention behavior on silica gel and florisil was investigated using diverse mobile-phase solvents and accounting for matrix effects. The beta-diastereomer, relative to the alpha- and gamma-diastereomers, is substantially retained on both florisil and silica gel regardless of the solvent used. The beta-diastereomer is therefore prone to undergo selective loss during clean-up. This sequence is counterintuitive to sequences based on reverse-phase chromatography with a C18-column, in which the alpha- (and not the beta-) isomer is eluted first when using a polar solvent. There has been some discrepancy regarding the structures of these diastereomers in the literature, with structures based on X-ray crystallography only becoming recently available. Based on these X-ray crystal structures, physical-chemical properties (the octanol-water partitioning constant, the Henrys law constant, subcooled liquid vapour pressures and subcooled liquid water solubilities) of the HBCD diastereomers were estimated using the quantum-chemistry based software COSMOtherm, and were found to differ from previously calculated values using different structures (e.g. log K(aw) for alpha-, beta-, and gamma-HBCD are here estimated to be -8.3, -9.3 and -8.2 respectively). Hypothesis relating differences in structure to physical-chemical properties and retention sequences are presented. The extra retention of the beta-diastereomer on silica gel and florisil is likely because it can form both greater specific (i.e. polar) and non-specific (i.e. non-polar) interactions with surfaces than the other diastereomers. Non-specific interactions can also account for the counter-intuitive elution orders with C(18)-reverse-phase chromatography. These results indicate that care should be taken when isolating HBCDs and other molecular diastereomers from environmental and biological samples, and that reported concentrations of beta-HBCD in the literature may be negatively biased.

High Concentrations of Organic Contaminants in Air from Ship Breaking Activities in Chittagong, Bangladesh

The beaches on the coast of Chittagong in Bangladesh are one of the most intense ship breaking areas in the world. The aim of the study was to measure the concentrations of organic contaminants in the air in the city of Chittagong, including the surrounding ship breaking areas using passive air samplers (N = 25). The compounds detected in the highest amounts were the polycyclic aromatic hydrocarbons (PAHs) and short-chain chlorinated paraffins (SCCPs), whereas dichlorodiphenyltrichloroethanes (DDTs), hexachlorobenzene (HCB), and polychlorinated biphenyls (PCBs) were several orders of magnitude lower in comparison. PCBs, PAHs, and HCB were highest at sites near the ship breaking activities, whereas DDTs and SCCPs were higher in the urban areas. Ship breaking activities likely act as atmospheric emission sources of PCBs, PAHs, and HCB, thus adding to the international emphasis on responsible recycling of ships. Concentrations of PAHs, PCBs, DDTs, HCB, and SCCPs in ambient air in Chittagong are high in comparison to those found in similar studies performed in other parts of Asia. Estimated toxic equivalent quotients indicate elevated human health risks caused by inhalation of PAHs at most sites.

Brominated Flame Retardants (BFR) in the Nordic Environment

The present report describe the results of screening analyses of the occurrence of ”new” brominated flame retardants (BFRs) in environmental samples from the Nordic countries. The aim of the screening was to establish whether, and if then to what extent, the non-polybrominated diphenyl eters BFRs are present at detectable levels in the environment. If the substances subjected for screening are found in amounts which are potentially harmful for the environment this will be followed up on national level. The Nordic screening project is run by a project group with representatives from the National Environmental Research Institute, University of Aarhus Denmark, the Finnish Environment Institute, the Environment and Food Agency of Iceland, the Environment Agency of the Faroe Islands, the Norwegian Climate and Pollution Agency and the Swedish Environmental Protection Agency. The project is supported by the Nordic Chemicals Group and the Aquatic Ecosystems Group as well as the participating institutions. The chemical analyses have been carried out jointly by the Norwegian Institute for Air Research (NILU) and the Swedish Environmental Research Institute (IVL).

Polychlorinated Alkanes in Fish from Norwegian Freshwater

Short-chain polychlorinated alkanes (sPCAs) have been measured in freshwater fish samples from different lakes all over Norway and from the Norwegian Arctic. The analyses were performed with high-resolution GC coupled to high-resolution MS in electron capture negative ion mode. The species investigated were trout, Arctic char, and burbot (Lota lota). Muscle tissue in the lake trout and Arctic char, and liver in burbot, were selected for analyses because of their high lipid content. ∑sPCA concentration ranged from 108 to 3700 ng/g fat. The highest value was found in the south of Norway near an industrial area.

Atmospheric short-chain-chlorinated paraffins in Melbourne, Australia – first extensive Southern Hemisphere observations

Environmental context This study presents the first comprehensive set of ambient atmospheric concentrations of short-chain-chlorinated paraffins in the Southern Hemisphere. The data show a seasonal cycle with a summer maximum and a winter minimum. The seasonal cycle is consistent with temperature dependence of the vapour pressure of the short-chain-chlorinated paraffins resulting in partitioning between the atmosphere and other reservoirs with a secondary modulation by soil moisture. Abstract The first extensive measurements of short-chain chlorinated paraffins (SCCPs) in the atmosphere of the Southern Hemisphere are presented. The analytical and sampling methodologies used in this Australian study were verified by systematic testing along with two inter-comparisons with Northern Hemisphere laboratories with established SCCP programs. In the ambient atmosphere of Melbourne, Australia, in 2013–14, there was a clear seasonal cycle in SCCP monthly averaged concentrations, these ranging from 28.4ng m–3 in summer to 1.8ng m–3 in winter. Air temperature was the factor most closely related to the seasonal cycle in SCCPs in Melbourne. The average SCCP concentrations observed indoors were less than those observed outdoors. Atmospheric concentrations of SCCPs in Melbourne are more than two orders of magnitude higher than concentrations in the background atmosphere. Surprisingly, the SCCP concentrations in Melbourne are similar to those observed in cities in Japan, South Korea and the United Kingdom, and less than those observed in China. Direct transport of SCCPs in the atmosphere from the Northern Hemisphere emissions to Melbourne is ruled out. Instead elevated concentrations in the Melbourne air-shed are most likely a result of the long-term import of SCCPs as industrial chemicals and within manufactured materials from the Northern Hemisphere so that the use of SCCPs in Melbourne and their consequent release to the environment has produced environmental reservoirs of SCCPs in Melbourne that are comparable with those in some Northern Hemisphere cities. The increase in SCCP concentrations from winter to summer is consistent with the temperature dependence of partitioning of SCCPs between the atmosphere and other reservoirs. Insufficient information exists on SCCP use and its presence in soils and sediments in Australia to indicate whether the atmospheric presence of SCCPs in Melbourne is a legacy issue due to its import and use as a metal cutting agent in past decades or due to ongoing imports of manufactured materials containing SCCPs today.