Effects of forest fire on the level and distribution of PCDD/Fs and PAHs in soil

Forest fires are believed to produce polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs); however, there is no firm evidence supporting this conjecture. To address this issue, we investigated whether PCDD/Fs and polycyclic aromatic hydrocarbons (PAHs) are formed by forest fires. The present work takes the indirect approach of measuring the levels of PCDD/Fs and PAHs in soil and ash samples 1, 5 and 9 months after forest fires. To determine if PCDD/Fs or PAHs were formed during forest fires, the levels of PCDD/Fs and PAHs measured in the burnt soil samples were compared with those in the corresponding unburnt soil samples. One month after forest fires, the concentrations of PCDD/Fs and PAHs in burnt soils were higher than in the corresponding unburnt soils. In addition, the homologue profiles differed between the burnt and unburnt soils. Five months after forest fires, however, the concentrations of PCDD/Fs and PAHs in the burnt soils were similar to those in unburnt soils. The data presented here strongly suggest that PCDD/Fs and PAHs form during forest fires and are then introduced into the soil. The results further suggest that the ash resulting from the combustion of wood and other organic matter is the main agent influencing the concentration of PCDD/Fs and PAHs in the soil.     

Semivolatile organic compounds in French schools: Partitioning between the gas phase,airborne particles and settled dust

The indoor environmental quality in classrooms can largely affect children's daily exposure to indoor chemicals in schools. To date, there has not been a comprehensive study of the concentrations of semivolatile organic compounds (SVOCs) in French schools. Therefore, the French Observatory for Indoor Air Quality (OQAI) performed a field study of SVOCs in 308 nurseries and elementary schools between June 2013 and June 2017. The concentrations of 52 SVOCs, including phthalates, polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons (PAHs), synthetic musks, and pesticides, were measured in air and settled dust (40 SVOCs in both air and dust, 12 in either air or dust). The results showed that phthalates had the highest concentrations among the SVOCs in both the air and dust. Other SVOCs, including tributyl phosphate, fluorene, phenanthrene, gamma-hexachlorocyclohexane (gamma-HCH, lindane), galaxolide, and tonalide, also showed high concentrations in both the air and dust. Theoretical equations were developed to estimate the SVOC partitioning between the air and settled dust from either the octanol/air partition coefficient or the boiling point of the SVOCs. The regression constants of the equations were determined using the data set of the present study for phthalates and PAHs.     

Concentrations of polybrominated diphenyl ethers, polychlorinated dibenzo-p-dioxins and dibenzofurans, and polychlorinated biphenyls in human blood samples from Korea

Analysis of blood samples is an effective way of evaluating contamination by persistent pollutants such as polybrominated diphenyl ethers (PBDEs), polychlorinated dibenzo-p-dioxin/furans (PCDD/Fs), and polychlorinated biphenyls (PCBs) in human population. Concentrations of PBDEs, PCDD/Fs and PCBs were measured in the blood of laborers (n = 13) working full time in two different municipal waste incinerator (MWI) plants and residents from the general population (n = 22) living in areas near MWIs in Korea. The concentrations of PBDEs were found to be slightly higher in the blood of incineration workers (8.61-46.05 ng/g lipid; mean, 19.33 ng/g lipid; median, 15.94 ng/g lipid) in comparison to that of residents from the general population (7.24-28.89 ng/g lipid; mean, 15.06 ng/g lipid; median, 14.34 ng/g lipid). The total average PCDD/Fs and PCB TEQ concentration was 20.11 pg/g lipid, averaged over incineration workers (17.73 pg/g lipid) and the general population (21.52 pg/g lipid). In addition, the average total crude concentration of PCDD/Fs was 7.40 ng/g lipids, which was 4.1 times greater than for PBDEs. Congener specific analysis confirmed that BDE 47 was a predictive indicator for total PBDE concentration (correlation coefficient r = 0.912), and that PCB 153 was a predictive indicator for total PCB concentration (r = 0.967). The PBDE levels in human blood in Korea are much higher than those reported in other countries. The presence of the BDE 183 congener was characteristic in the blood of workers from an electronic dismantling facility in MWIs.     

Persistent organic pollutants in ringed seals from the Russian Arctic

Organochlorine compounds total DDT (ΣDDT), total HCH isomers (ΣHCH), toxaphenes (sum of Parlar 26, 50, 62), mirex, endrin, methoxychlor, total chlorinated benzenes (ΣCBz), total chlordane compounds (ΣCHL), polychlorinated biphenyls (total of 56 congeners; ΣPCBs), polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs), and polybrominated diphenyl ethers (sum of 7 tri- to hepta congeners; ΣPBDEs) were analysed in the blubber of adult ringed seals from the four areas of the Russian Arctic (White Sea, Barents Sea, Kara Sea and Chukchi Sea) collected in 2001-2005. Ringed seals from the south-western part of the Kara Sea (Dikson Island — Yenisei estuary) were the most contaminated with ΣDDTs, ΣPCBs, ΣCHL, and mirex as compared with those found in the other three areas of Russian Arctic, while the highest mean concentrations of ΣHCHs and PCDD/Fs were found in the blubber of ringed seals from the Chukchi Sea and the White Sea, respectively. Among all organochlorine compounds measured in ringed seals from the European part of the Russian Arctic, concentrations of ΣDDT and ΣPCBs only were higher as compared with the other Arctic regions. Levels of all other organochlorine compounds were similar or lower than in seals from Svalbard, Alaska, the Canadian Arctic and Greenland. ΣPBDEs were found in all ringed seal samples analysed. There were no significant differences between ΣPBDE concentrations found in the blubber of ringed seals from the three studied areas of the European part of the Russian Arctic, while PBDE contamination level in ringed seals from the Chukchi Sea was 30-50 times lower. ΣPBDE levels in the blubber of seals from the European part of the Russian Arctic are slightly higher than in ringed seals from the Canadian Arctic, Alaska, and western Greenland but lower compared to ringed seals from Svalbard and eastern Greenland.     

Evidence for the transfer of polychlorinated biphenyls, polychlorinated dibenzo-p-dioxins, and polychlorinated dibenzofurans from soil into biota

The concentrations of six indicator and co-planar polychlorinated biphenyls (PCBs), 17 polychlorinated dibenzo-p-dioxins, and polychlorinated dibenzofurans (PCDD/Fs) were determined in soil and associated biota samples collected from a polluted and wasted farmland in southern China. The sum of six indicator PCBs (Nos 28, 52, 101, 138, 153 and 180) concentrations in biota samples were proportional to the total amount of PCBs that transferred from soil to the corresponding biota samples, and the sum six indicator PCB congeners in samples were about 20% of the total PCBs, respectively. The ratios of the sum six indicator PCBs and the total PCBs in samples collected in the same area were approximately equal. The sums of six indicator PCBs were proportional to the total PCBs that transferred from soil to plant, while the co-planar PCBs were not. Analysis of individual PCB and PCDD/F congener signatures in soil revealed the original pollutant source after transportation and biodegradation for 14 years using principal component analysis (PCA). The pattern of PCBs in soils and plants could reflect the original pollution source after transportation and biodegradation for 14 years, while the pattern of PCBs in the terrestrial animals could not reflect the primary source. The consumption foods in this region such as foraging chicken eggs, foraging duck eggs, and loach (Misgurnus anguillicaudatus) were highly contaminated, the total toxicity equivalent (TEQ) was up to 784 pg WHO-TEQ/g on basis lipid in foraging chicken eggs.     

The role of UV-B on the degradation of PCDD/Fs and PAHs sorbed on surfaces of spruce (Picea abies (L.) Karst.) needles

Photodegradation of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and polycyclic aromatic hydrocarbons (PAHs) sorbed on surfaces of spruce (Picea abies (L.) Karst.) needles was investigated. The role of sunlight and, in particular, the role of short wavelength UV-B radiation were studied in a sun simulator under controlled environmental conditions. The photodegradation of PCDD/Fs and PAHs follows first-order kinetics. Simulated sunlight containing UV-B induced two phases of photodegradation kinetics for PCDD/Fs, whereas no distinct phases of the kinetics were observed for PAHs. UV-B radiation plays a much more important role on the photodegradation for PCDD/Fs than that for PAHs. Direct photolysis dominates the photodegradation of PCDD/Fs and PAHs.     

Measurement of atmospheric PCDD/F and PCB distributions in the vicinity area of Waelz plant during different operating stages

A comprehensive sampling program was conducted at four sampling sites in the vicinity area of a Waelz plant prior to and after the retrofitting of this plant for reducing PCDD/F (polychlorinated dibenzo-p-dioxin and polychlorinated dibenzofuran) and polychlorinated biphenyl (PCB) emission to evaluate its effects on atmospheric PCDD/F and PCB concentrations. During the shutdown stage of the Waelz plant investigated, the atmospheric PCDD/F and PCB concentrations measured in the vicinity area (sites A, B and C) range from 24 to 170 fg-I-TEQ/m(3) and 5.0 to 8.2 fg-TEQ(WHO)/m(3), respectively. As the facility restarted to operate, the atmospheric PCDD/F and PCB concentrations measured increased to 570-1460 fg-I-TEQ/m(3) and 23-59 fg-TEQ(WHO)/m(3), respectively. When activated carbon injection (ACI) was adopted in the facility in early 2006, the PCDD/F concentrations measured in stack gas decreased dramatically from 190 to 3.4 ng-I-TEQ/Nm(3), while the PCB concentrations decreased from 4.9 to 0.08 ng-TEQ(WHO)/Nm(3). In the meantime, the atmospheric PCDD/F and PCB concentrations measured at sites A, B and C decreased to 150-340 fg-I-TEQ/m(3) and 13-19 fg-TEQ(WHO)/m(3), respectively. However, relatively high PCDD/F (180-1460 fg-I-TEQ/m(3)) and PCB (9.3-59 fg-TEQ(WHO)/m(3)) concentrations were measured at site D during all sampling stages. Overall, atmospheric sampling results indicate that over 50% of PCDD/Fs distributed in solid phase, while over 90% of PCBs distributed in vapor phase during all sampling stages.     

Modern and historical fluxes of halogenated organic contaminants to a lake in the Canadian arctic, as determined from annually laminated sediment cores

Two annually laminated cores collected from Lake DV09 on Devon Island in May 1999 were dated using 210Pb and 137Cs, and analyzed for a variety of halogenated organic contaminants (HOCs), including polychlorinated biphenyls (PCBs), organochlorine pesticides, short-chain polychlorinated n-alkanes (sPCAs), polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), and polybrominated diphenyl ethers (PBDEs). Dry weight HOC concentrations in Lake DV09 sediments were generally similar to other remote Arctic lakes. Maximum HOC fluxes often agreed well with production maxima, although many compound groups exhibited maxima at or near the sediment surface, much later than peak production. The lower than expected HOC concentrations in older sediment slices may be due to anaerobic degradation and possibly to dilution resulting from a temporary increase in sedimentation rate observed between the mid-1960s and 1970s. Indeed, temporal trends were more readily apparent for those compound classes when anaerobic metabolites were also analyzed, such as for DDT and toxaphene. However, it is postulated here for the first time that the maximum or increasing HOC surface fluxes observed for many of the major compound classes in DV09 sediments may be influenced by climate variation and the resulting increase in algal primary productivity which could drive an increasing rate of HOC scavenging from the water column. Both the fraction (F(TC)) and enantiomer fraction (EF) of trans-chlordane (TC) decreased significantly between 1957 and 1997, suggesting that recent inputs to the lake are from weathered chlordane sources. PCDD/Fs showed a change in sources from pentachlorophenol (PeCP) in the 1950s and 1960s to combustion sources into the 1990s. Improvements in combustion technology may be responsible for the reducing the proportion of TCDF relative to OCDD in the most recent slice.     

Persistent organohalogen contaminant burdens in Antarctic krill (Euphausia superba) from the eastern Antarctic sector: a baseline study

A baseline for persistent organohalogen compound (POC) accumulation in the Antarctic keystone species, Antarctic krill (Euphausia superba) has been established for a 50 degrees longitudinal range of the eastern Antarctic sector. Samples of adult krill, caught from 12 sites distributed between 30 degrees and 80 degrees E (60-70 degrees S), were analysed for >100 organohalogen compounds including chlorinated pesticides, polychlorinated biphenyls (PCBs), polybrominated organic compounds and polychlorinated dibenzo-p-dioxins/furans (PCDD/Fs). Organochlorine pesticides dominated measured krill contaminant burdens with hexachlorobenzene (HCB) as the single most abundant compound quantified. Krill HCB concentrations were comparable to those detected at this trophic level in both the Arctic and temperate northwest Atlantic, lending support for the hypothesis that HCB will approach global equilibrium at a faster rate than other POCs. Para, para'-dichlorodiphenylethene (p,p'-DDE) was detected at notable concentrations. Measurements of DDT and its degradation products provide an important baseline for monitoring the temporal and geographical influence of renewed, DDT usage for malaria-control in affected southern hemisphere countries. In contrast to the Arctic, PCBs did not feature prominently in contaminant burdens of Antarctic krill. The major commercial polybrominated diphenyl ether (PBDE) congeners -99 and -47 were quantified at low background levels with clear concentration spikes observed at around 70 degrees E , in the vicinity of modern, active research stations. The likelihood that local anthropogenic activities are supplementing low PBDE levels, delivered otherwise primarily via long range environmental transport, is discussed. The suspected naturally occurring brominated organic compound, 2,4,6-tribromoanisole (TBA), was a ubiquitous contaminant in all samples whereas the only PCDD/Fs quantifiable were trace levels of octachlorodibenzo-p-dioxin (OCDD) and 1,2,3,4,7,8/1,2,3,4,7,9-hexachlorodibenzofuran (HxCDF). With the aims of; i) Generating a robust and broadly applicable POC auditing platform for the scarcely studied eastern Antarctic sector; ii) Determining the compounds accumulating in Antarctic krill for further toxicity evaluation studies and iii) Establishing a baseline for Antarctic predator exposure to POCs, this study represents one of the most comprehensive reports of POC contamination of the Antarctic food web to date.     

Persistent organic pollutants and mercury in dead and dying glaucous gulls (Larus hyperboreus) at Bjørnøya (Svalbard)

Dead and dying glaucous gulls (Larus hyperboreus) were collected on Bjørnøya in the Barents Sea in 2003, 2004 and 2005. Autopsies of the seabirds only explained a clear cause of death for three (14%) of the 21 birds. A total of 71% of the birds were emaciated. Liver and brain samples were analysed for organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), polybrominated diphenyl ether (PBDEs), hexabromocyclododecanes (HBCDs) and mercury (Hg). High levels of ΣOCPs, ΣPCBs, ΣPBDEs and α-HBCD were found in liver and brain. Compared to the dead and dying glaucous gulls found 1989, the congeners' composition tended to change toward more persistent compounds in the 2003–2005 samples. The brain levels of OCPs and PCBs did not differ between 1989 and 2003–2005, while the liver levels were significantly lower. The brain/liver ratio for PCB and PBDE significantly decreased with halogenations of the molecule, indicating a clear discrimination of highly halogenated PCBs and PBDEs entering the brain. There was further a clear negative correlation between contaminant concentrations and body condition. The brain levels were not as high as earlier published lethal levels of p,p′-DDE or PCB. However, more recent studies reported a range of sub-lethal OCP- and PCB-related effects in randomly sampled glaucous gulls. An additional elevation of pollutants due to emaciation may increase the stress of the already affected birds. The high brain levels of OCP, PCB and PBDE of present study might therefore have contributed to the death of weakened individuals of glaucous gull.     

Semi‐volatile organic compounds in the air and dust of 30 French schools: a pilot study

The contamination of indoor environments with chemical compounds released by materials and furniture, such as semi‐volatile organic compounds (SVOCs), is less documented in schools than in dwellings—yet children spend 16% of their time in schools, where they can also be exposed. This study is one of the first to describe the contamination of the air and dust of 90 classrooms from 30 nursery and primary schools by 55 SVOCs, including pesticides, phosphoric esters, musks, polycyclic aromatic hydrocarbons (PAHs), polychlorobiphenyls (PCBs), phthalates, and polybromodiphenylethers (PBDEs). Air samples were collected using an active sampling method, and dust samples were collected via two sampling methods (wiping and vacuum cleaning). In air, the highest concentrations (median >100 ng/m³) were measured for diisobutyl phthalate (DiBP), dibutyl phthalate (DBP), diethyl phthalate (DEP), bis(2‐ethylhexyl) phthalate (DEHP), and galaxolide. In dust, the highest concentrations (median >30 μg/g) were found for DEHP, diisononyl phthalate (DiNP), DiBP, and DBP. An attempt to compare two floor dust sampling methods using a single unit (ng/m²) was carried out. SVOC concentrations were higher in wiped dust, but frequencies of quantification were greater in vacuumed dust.     

Increases in ambient PCDD/F and PCB concentrations in Northern Taiwan during an Asian dust storm episode

In spring 2006, an Asian dust storm (ADS) that originated in the deserts of Mongolia and China eventually reached populated areas of East Asia, including Taiwan. The concentrations of total suspended particles (TSP), vapor/solid-phase dioxin-like compounds and metal content in atmospheric aerosols were monitored at two sampling sites in northern Taiwan during the ADS episode: one along the northern coast (Site A), and the other in Taipei city (Site B). The ADS swept across northern Taiwan from 13 March to 19 March, 2006. Data indicate that the atmospheric dibenzo-p-dioxin and dibenzofuran (PCDD/F, 32.2 to 52.5 fg-I-TEQ/m(3)) and polychlorinated biphenyl (PCB, 2.23 to 4.49 fg-TEQ(WHO)/m(3)) concentrations measured at the two sampling sites prior to the ADS episode were considerably lower than those measured in other Asian countries. However, measurements made at both sites on 13 and 18 March 2006 indicate that the atmospheric PCDD/F and PCB concentrations increased 2.5 and 3.2 times at Site A, and 2.1 and 1.9 times at Site B, respectively, during the ADS episode. The concentrations of aluminum (Al), potassium (K) and Titanium (Ti) in atmospheric aerosols were also found to increase about 2 to 5 times during this period. As no specific dioxin emission sources exist within nearly 20 km of Site A, the increase in PCDD/F and PCB concentrations observed there is likely to be related to the ADS from mainland China. Additionally, the amount of PCDD/Fs bound to suspended particles increased from 257-259 to 339-512 pg-I-TEQ/g-TSP during the ADS episode. The distribution of OCDD congener observed in Taipei city increased dramatically during the ADS episode, however, the distribution of PCB congener did not vary significantly.     

Interpreting the dioxin and furan profiles in the lichen Ramalina canariensis Steiner for monitoring air pollution

The purpose of this study was to compare the dioxin and furan (PCDD/F) profiles in lichens with those of air and soil. Lichen samples of the species Ramalina canariensis Steiner were collected from 44 different sites and analysed. The results were compared to PCDD/F air and soil profiles from bibliographic data concerning several countries and locations. When compared to other biomonitors (pine needles, vegetation, fruits), lichens were observed to accumulate greater concentrations of PCDD/Fs. The results showed that, although the concentrations of PCDD/Fs in lichens were at the same level of magnitude as those found for soils from the same country (197.5-1218.7 ng kg(-1) and 2.3-15.2 ng I-TEQ kg(-1)), the PCDD/Fs profiles do not reflect soil particle contamination. On the contrary, the PCDD/Fs lichen profiles seemed to be very similar to the ones in the air, at least for the diversity of the ones used for comparison in this study. These results indicated that lichens of the species R. canariensis are potential biomonitors of PCDD/F air pollution.     

Characteristics of PCDD/F congener distributions in gas/particulate phases and emissions from two municipal solid waste incinerators in Taiwan

Partitioning of PCDD/F (polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofuran) congeners between gaseous and particulate phases and removal efficiencies of the existing air pollution control devices (APCDs) for PCDD/Fs at two large-scale municipal waste incinerators (MWIs) in Taiwan are evaluated via stack sampling and analysis. Two MWIs investigated are equipped with activated carbon injection (ACI) and selective catalytic reduction system (SCR) as major PCDD/F control devices, respectively. The average PCDD/F concentrations of stack gases are 2.35 and 1.49 ng/N m(3), and the international toxic equivalent quantity (TEQ) are 0.17 and 0.043 ng TEQ/N m(3) in MWI-A and MWI-B, respectively. The average removal efficiency of PCDD/Fs achieved with ACI+BF (bag filters) reaches 95% (MWI-A) while that achieved with the WS (wet scrubber)+SCR system reaches 99% (MWI-B). The results obtained on gas/particulate partitioning in flue gases indicate that particulate-phase PCDD/Fs accounted for 27.7% and 24.7% of the total PCDD/F concentrations at the outlets of cyclone (CY) and electrostatic precipitator (EP) for MWI-A and MWI-B, respectively. But the gas/particulate partitioning in flue gas after PCDD/Fs control devices is quite different in two MWIs. This study also indicates that total 2,3,7,8-substituted PCDD/F discharges are 142.3 microg TEQ/ton waste for MWI-A and 98.6 microg TEQ/ton waste for MWI-B, respectively.     

Assessment of human exposure to indoor organic contaminants via dust ingestion in Pakistan

Ingestion of indoor dust has been acknowledged as an important route of exposure to organic contaminants (OCs). We investigated the presence of polybrominated diphenyl ethers (PBDEs), novel brominated flame retardants (NBFRs), organophosphate flame retardants (OPFRs), polychlorinated biphenyls (PCBs), and organochlorine pesticides (OCPs) in indoor floor dust from rural homes (N=31) and mosques (N=12) in Gujrat, Pakistan. Low concentrations were observed for most contaminants. OPFRs were the principle contaminants, with tri-(2-butoxyethyl)-phosphate (TBEP) and tri-phenyl-phosphate (TPP) having medians of 66 and 109 ng/g, respectively. PBDEs were only minor constituents in the investigated samples, with BDE 209 (median 40 ng/g) being the most important congener. Levels and profile of ∑PBDEs, ∑NBFRs, ∑HCHs, ∑DDTs, and ∑PCBs revealed no difference (P<0.05) between samples of dust from homes and mosques, indicating similar emission sources. Exposure scenarios using 5th percentile, median, mean, and 95th percentile levels were estimated for both adult and toddlers. Typical high-end, using median levels and high dust ingestion, exposure for adults were 0.02, 0.02, 0.03, <0.01, and 0.65 ng/kg bw/day and for toddlers 0.39, 0.45, 0.69, 0.01, and 15.2 ng/kg bw/day for ∑PBDEs, ∑NBFRs, ∑OCPs, ∑PCBs, and ∑OPFRs, respectively. To the authors' knowledge, this is the first study to document the presence of indoor OCs in Pakistani dust. PRACTICAL IMPLICATIONS: This is the first report on the analysis of various contaminants in indoor dust from Pakistan. Some of these chemicals are currently being used in different consumer products. The study will help to further an understanding of the levels of different organic contaminants (OCs) in Pakistani indoor environments and will enlighten the generally ignored area of environmental pollution in Pakistan. Furthermore, studies based on animal models have shown that some of the analyzed chemicals can cause different types of chronic toxicities. However, our results showed that the levels of estimated exposure via dust ingestion for all chemicals were several orders of magnitude lower than their reference dose (RfD) values or than those reported in studies from Belgium, China, Singapore, and the UK (Ali et al., 2011a; Harrad et al., 2008; Tan et al., 2007a,b; Van den Eede et al., 2011a; Wang et al., 2010).     

Spatial and temporal changes of chlorinated pesticides, PCBs, dioxins (PCDDs/PCDFs) and brominated flame retardants in human breast milk from Northern Russia

This study presents for the first time temporal changes of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in Russian human breast milk samples. Concentrations of OCPs and PCBs in samples from three locations in the North West of Russia in 2000-2002 (n=42), were compared to corresponding levels measured in 1993-1996 (n=58). In addition brominated flame retardants (BFRs), consisting of polybrominated diphenylethers (PBDEs) (including BDE-209) and hexabromocyclododecane (HBCD) were analysed in samples from 2000-2002 (n=37). The present levels of SigmaDDTs and SigmaHCHs were 5 and 10 times higher than corresponding levels in the neighbouring country Norway. Median concentrations of SigmaHCHs (196 microg/kg lw), SigmaCHBs (19.7 microg/kg lw) and SigmaPCBs(16) (316 microg/kg lw) were highest in Murmansk. The percentage of p,p'-DDT to SigmaDDTs and ratio DDE/DDT suggest possible ongoing use of DDT in Russia. Levels of PBDE were low and dominated by the congeners BDE-47 and BDE-153. The deca brominated BDE-209 was detected in all analysed samples (median concentration 0.19 microg/kg lipid). Levels of SigmaOCPs and SigmaPCBs decreased 56 and 30% in Murmansk and 36 and 43% in Arkhangelsk during the study period. The decline of SigmaOCPs was significant at both locations (p<0.05-p<0.0001). For SigmaPCBs, the decreasing trend was only significant in Arkhangelsk (p<0.0001). In addition, a decline of Sigmatotal TEQs (SigmaTEQs of PCDDs/PCDFs, non-ortho- and mono-ortho PCBs) was observed in Murmansk and Arkhangelsk during the study period. The exposure of infants by PCDDs/PCDFs and dioxin-like PCBs is still exceeding the daily tolerable intake (TDI) in North West Russia. However, the concentrations of PCDDs/PCDFs and dioxin-like PCBs seem to decline very rapidly.     

The use of blue tit eggs as a biomonitoring tool for organohalogenated pollutants in the European environment

In the present study, large scale geographical variation in the occurrence of organohalogenated pollutants (OHPs) was investigated throughout Europe using eggs of a terrestrial resident passerine species, the blue tit (Cyanistes caeruleus). Blue tit eggs from 10 sampling locations, involving suburban, rural and remote areas, in 7 European countries were collected and analysed. Sum polychlorinated biphenyl (PCB) levels ranged from 150 ng/g lipid weight (lw) to 2003 ng/g lw. Sum polybrominated diphenyl ethers (PBDEs) ranged from 3.95 ng/g lw to 114 ng/g lw. As expected, PCB and PBDE concentrations were significantly higher in the sampled suburban locations compared to the rural and remote locations. Sum organochlorine pesticides (OCPs) ranged from 122 ng/g lw to 775 ng/g lw. OCP concentrations were, against the expectations, found to be lower in the rural sampling locations compared to the other locations. Contamination profiles of PCBs, PBDEs and OCPs differed also among the sampling locations, which may be due to local contamination sources. Finally, we compared the results of this study with previously reported OHP concentrations in the eggs of a closely related species, the great tit (Parus major), from the same sampling locations in Europe. We found no differences in concentrations between the species. In addition, we found a significant, positive correlation between the sum PCB concentrations in blue tit eggs and great tit eggs, suggesting similar exposure pathways, mechanisms of accumulation and maternal transfer of PCBs. In conclusion, our results suggest the usefulness of eggs from passerine birds as a biomonitoring tool for OHPs on a large geographical scale.     

Bioaccumulation of polychlorinated dibenzo-p-dioxins, dibenzofurans, and dioxin-like polychlorinated biphenyls in fishes from the Tittabawassee and Saginaw Rivers, Michigan, USA

Characterizing biological factors associated with species-specific accumulation of contaminants is one of the major focuses in ecotoxicology and environmental chemistry studies. In this study, polychlorinated dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and non- and mono-ortho-substituted polychlorinated biphenyl (PCB) congeners were analyzed in various fish species from the Tittabawassee and Saginaw Rivers (12 fish species; n = 314 individuals), Michigan, USA. Due to their migratory habits, greater δ¹³C stable isotope values were found in walleye and white sucker among 12 fish species. Meanwhile, the δ¹⁵N values indicated that the trophic status was least in carp and greatest in largemouth bass. The greatest total concentrations of dioxins were found in fishes with the lowest trophic status (carp (n = 50) followed by channel catfish (n = 49)), and concentrations of ΣPCDD/Fs (20-440 pg/g ww (wet weight)), ΣPCBs (16-690 ng/g ww), and TEQs (6.8-350 pg/g ww) in carp were also greater than the least mean concentrations in other fishes. Contributions of various biological factors to the species accumulation were assessed. Body weight and lipid content were found to be the most significant factors influencing accumulation of ΣPCDD/Fs. Lipid content and trophic level seemed to be dominant factors determining accumulation of ΣPCB and TEQs, but negative correlations between trophic status and concentrations of ΣPCBs and TEQs were observed possibly due to the great concentrations in benthivorous fishes such as carp occupying lower trophic levels. These factors can be used to predict the contaminant levels of dioxins and health risks of the fishes in the river ecosystem.     

Polybrominated diphenyl ethers and polychlorinated biphenyls in indoor dust in Durban,South Africa

Polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) were measured in indoor dust of three microenvironments in Durban, South Africa. The sum of eight PBDEs and three PCBs were quantified by gas chromatography with mass spectral detection. The mean concentrations of ∑_n = 8 PBDEs and ∑_n = 3 PCBs in 10 homes, 11 offices, and 13 university students’ computer laboratories were 1710, 1520, and 818 ng/g, and 891, 923, and 1880 ng/g for PBDEs and PCBs, respectively. The concentration of PCBs found in homes was independent (P = 0.0625) of building construction year. Similarly, no relationship was observed between PCB concentrations and floor type. The concentrations of PBDEs correlated (r = 0.60) with PCB concentrations in homes, thus assuming similar sources. The elevated concentrations of PBDEs and PCBs may have significant implications for human exposure.     

Occurrence and removal of selected organic micropollutants at mechanical, chemical and advanced wastewater treatment plants in Norway

In Norway the combined hydraulic capacity of all domestic wastewater treatment plants is relatively equally distributed between three major treatment plant types; mechanical, chemical, and combined chemical and biological. The Western coast from Lindesnes in the south to the Russian boarder in the North is dominated by mechanical treatment plants, constituting approximately 68% of the treatment capacity in that area. In the present study we report concentrations and removal efficiencies of polycyclic aromatic hydrocarbons (PAHs), nonylphenols, phthalates, polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) found in five Norwegian wastewater treatment plants (WWTPs) applying different levels of treatment. Concentrations of organic micropollutants in the influents to the WWTPs were generally in the low range of what have been reported by others for domestic wastewater in Europe and North-America. More than 90% removal could be obtained for nonylphenols, PBDEs, and the more hydrophobic 4-6 ring PAHs by chemical precipitation, however, biological treatment appeared to be necessary for efficient removal of the less lipophilic 2 and 3 ring PAHs, the medium- to short-chained nonylphenol ethoxylates and diethyl phthalate. SigmaPCB(7) was removed by more than 90% by combined biological/chemical treatment, while removal efficiency by chemical treatment was not possible to estimate due to low inlet concentrations. Low or insignificant removals of PAHs, phthalates and nonylphenols with their ethoxylates were observed at the mechanical WWTP, which was in accordance with the minuscule removal of TOC.