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A series of treatment experiments were carried out to evaluate the applicability of a high-temperature melting treatment (GeoMelt process) to the destruction of polychlorinated naphthalene (PCN) formulation. We started with 10-kg-scale experiments in which a small melting furnace was used and then scaled up to a 1-t-scale experiment in which a melting furnace that resembled an actual treatment system was used. These runs were evaluated whether destruction efficiency (DE) of total PCNs was more than 99.999 % and whether concentrations of PCNs and polychlorinated dibenzo- p-dioxins/dibenzofurans (PCDDs/DFs) in vitrified materials, emission gas, and scrubber water were below the target levels. Because DE values and the target levels of PCNs and PCDDs/DFs in these runs were satisfactory, then we carried out a demonstrative experiment using the actual treatment system and confirmed destruction of PCNs. Based on good results of the demonstrative experiment, stock of PCN formulation was successfully treated continuously. [ABSTRACT FROM AUTHOR]

Abstract: Air samples were collected in Venice during summer 2009 and 2012 to measure gas and particulate concentrations of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and polychlorinated naphthalenes (PCNs). PCB-11, considered a marker for non-Aroclor contamination of the environment, was found for the first time in the Venetian lagoon and in Europe. An investigation on sources has been conducted, evidencing traffic as the major source of PAHs, whereas PCBs have a similar composition to Aroclor 1248 and 1254; in 2009 a release of PCN-42 has been hypothesized. Toxicological evaluation by TCA and TEQ methods, conducted for the first time in Venice air samples, identified BaP, PCB-126 and PCB-169 as the most important contributors to the total carcinogenic activity of PAHs and the total dioxin-like activity of PCBs and PCNs. [Copyright &y& Elsevier]

Highlights: [•] Single-descriptor QSPRs with high robustness and external predictivity reported. [•] Total-energy and electron-correlation energy proved to be the best descriptors. [•] Correlation-energy is a good measure of intramolecular interactions for QSPR study. [•] For descriptor computation, advanced semiempirical methods found to be as reliable as ab inito. [•] Model based on descriptors computed with PM7 method are robust and predictive. [ABSTRACT FROM AUTHOR]

Highlights: [•] Adding (NH4)2SO4 caused reductions in WHO-TEQ concentrations. [•] The inhibiting effect was greater for PCDF than PCDD. [•] PCN formation was promoted when adding (NH4)2SO4. [ABSTRACT FROM AUTHOR]

Highlights: [•] PCN formation mechanisms during thermal processes are discussed. [•] PCN emission levels from a number of industrial thermal processes are compared. [•] PCN congener profiles from different sources are presented and compared. [•] PCN emission factors from a number of industrial thermal processes are summarized. [ABSTRACT FROM AUTHOR]

Abstract: Polychlorinated naphthalenes (PCNs) are now under review by the Stockholm Convention as candidates for persistent organic pollutants (POPs) due to their persistence, toxicity, bioaccumulation, and long-range atmospheric transport. Data on PCN levels are sparse in South Asia. Atmospheric PCNs in India and Pakistan were monitored during the winter by polyurethane foam disk passive air samplers (PUF-PAS). The average concentrations were 29pg/m3 and 7.7pg/m3 in the Indian and Pakistani samples, respectively. Those concentration levels were relatively lower than the previously reported values in other Asian countries, but still considerably higher than in other sites in the world. Tri-CNs and tetra-CNs were the dominant homologues in the air, especially in India. Spatially, the PCNs were ubiquitous in the target areas, and local distribution was generally impacted by the proximity to potential sources. Major sources of PCNs in this study were the re-emission of Halowax and industrial thermal processes. Biomass burning influenced some sites in Pakistan. However, the enrichment of tri-CNs in Indian cities cannot be ascribed to either the signature of a specific source or the preferential volatilization and/or photodegradation in tropical areas. Despite this unclear issue in South Asia, the present study indicates that the potential health impact was generally comparable to that in non-urban sites worldwide. [Copyright &y& Elsevier]

Abstract: This study investigated the seasonality of atmospheric polychlorinated biphenyls (PCBs) and polychlorinated naphthalenes (PCNs) in Japan. Polyurethane foam (PUF) disk passive air samplers (PAS) were deployed simultaneously at 55 sites in spring 2008, summer 2008 and winter 2008/09. Sampler deployment spanned 8 continuous weeks in each season. The non-outlier ranges of the two pollutants (ng/sample) were as follows; ∑190PCBs: 6.5–38.6 (spring), 43.5–220.5 (summer) and 25.9–136 (winter); and ∑63PCNs: 0.4–3.9 (spring), 0.7–7.1 (summer) and 1.1–9.2 (winter). The corresponding values in air were ∑190PCBs (pg m−3): 33–197 (spring), 222–1125 (summer) and 132–694 (winter); and ∑63PCNs (pg m−3): 2.2–20 (spring), 3.5–36 (summer) and 5.7–47 (winter), when sampling rate of 3.5 m3 day−1 was assumed. Thus, the PCBs peaked in summer, while the PCNs mostly peaked in winter; there was an apparent contrast in their seasonality in Japan. For the PCNs, seasonal variability was significant at rural than urban sites. Normally, POPs would show relatively increased air content in summer due to vaporization effect. The PCNs appeared to deviate from such a trend because of overriding input of tri-CNs presumably transported from long range by northwesterly winds in the winter season. The dioxin-like fractions of either pollutant were reduced in winter by about 30–50%. [Copyright &y& Elsevier]

Polychlorinated naphthalenes (PCNs) are both highly toxic and bioaccumulative environmental contaminates. Dietary intake is the primary pathway for human exposure to PCNs, and PCN concentrations in aquatic foodstuffs are relatively high. Chinese mitten crab (Eriocheir sinensis) is one kind of popular aquatic foodstuffs in Asian countries. Farmed crabs could exposure to PCNs both through feed and environment. However, information on the occurrence of PCNs in farmed crabs is scarce. The present study investigated 75 PCN congeners in farmed Chinese mitten crabs, crab compound feed and sediments collected from Anhui Province and Shanghai in China. The total PCN concentrations in farmed Chinese mitten crabs from Anhui Province and Shanghai were 11.2–42.2 and 5.46–43.8 pg/g wet weight (ww), respectively. The PCN homologue profiles in crabs from both areas were similar, and both were dominated by di-CNs and penta-CNs. In contrast, lower chlorinated PCNs (di-CNs, tri-CNs and tetra-CNs) were the most common homologues in specimens of crab compound feed and sediment samples, indicating that selective bioaccumulation and metabolism of PCNs might occur in farmed crabs. No regional differences were found in the PCN congener profiles of farmed crabs, feed and sediment samples taken from Anhui Province and Shanghai. An assessment found no significant health risk associated with Chinese exposure to PCNs through farmed Chinese mitten crab consumption. • PCN concentrations and patterns in farmed crabs from select regions were similar. • The predominant PCNs were di-CN and penta-CN homologues. • PCN concentrations were higher in sediment from the lower Yangtze River. • PCN patterns in crab feed and sediment were different from those in farmed crabs. • Human exposure to PCNs through consuming farmed crabs is likely to be minimal. [ABSTRACT FROM AUTHOR]

Highlights: [•] Fly ash was identified as a route of POPs release from the coking industry. [•] Emission factors were derived for unintentionally produced POPs in coking ash. [•] The data obtained were useful for developing an integrated source inventory. [•] Congener profiles for the unintentionally produced POPs in coking ash are presented. [ABSTRACT FROM AUTHOR]

Abstract: Polychlorinated naphthalenes (PCNs) belong to a group of dioxin-like pollutants; however little information is available on PCNs in North China. In this study, gridded field observations by passive air sampling at 90 sites were undertaken to determine the levels, spatial distributions, and sources of PCNs in the atmosphere of North China. A median concentration of 48 pg m−3 (range: 10–2460 pg m−3) for ∑29PCNs indicated heavy PCN pollution. The compositional profile indicated that nearly 90% of PCNs observed were from thermal processes rather than from commercial mixtures. Regarding the source type, a quantitative apportionment suggested that local non-point emissions contributed two-thirds of the total PCNs observed in the study, whereas a point source of electronic-waste recycling site contributed a quarter of total PCNs. The estimated toxic equivalent quantity for dioxin-like PCNs ranged from 0.97 to 687 fg TEQ m−3, with the electronic-waste recycling site with the highest risk. [Copyright &y& Elsevier]

The concentrations of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), dioxin-like polychlorinated biphenyls (dl-PCBs), and polychlorinated naphthalenes (PCNs) were determined in workplace air from eight secondary nonferrous metal processing plants to investigate occupational exposure to these toxic compounds. The total estimated daily intakes of PCDD/Fs and dl-PCBs for workers by inhalation in the workplace were in the range of 0.15-9.91 and 0.13-8.59 pg of WHO-TEQ/kg of body weight (bw) for moderate and light activities, respectively. The daily inhalation doses for workers in the workplaces of three investigated plants exceeded the tolerable daily intake recommended by the World Health Organization. These results indicate that the risk of occupational exposure to dioxins by inhalation in the workplace of plants investigated was considerably high. For PCNs, the daily inhalation doses for workers in the workplace were in the range of 0.005-4.46 and 0.004-3.87 pg of TEQ/kg of bw for moderate and light activities, respectively, which were lower than those of dioxins. To identify the source of PCDD/Fs, PCBs, and PCNs in workplace air, their homologue profiles were compared with those in stack gas from the plants investigated. It was found that significant dioxin contamination in workplace air was mainly attributed to the emission of fugitive gas from smelting furnaces during reclamation processes. [ABSTRACT FROM AUTHOR]

Abstract: Sucralose, an artificial sweetener, is being used in increasingly large amounts in foodstuffs and beverages worldwide. Information pertaining to its ability to participate in chlorination reactions during cooking and generate toxic compounds, however, is scarce. In this study, the formation and distribution of polychlorinated naphthalenes (PCNs), which are a group of highly toxic polychlorinated aromatic compounds, in oil heated in the presence of sucralose was investigated. The concentrations of the PCNs present in the cooking oils and oil fumes generated during the heating process were determined by isotope dilution according to a HRGC/HRMS method. The results suggested that the heating of cooking oil in the presence of sucralose promoted the formation of toxic PCNs. Although PCNs were detected in the oil fumes, no PCNs were found in the heated oils. The total concentrations of the PCNs found in peanut and olive oil fumes were 490 and 240 pg g−1, respectively. The degree of chlorination for the PCNs was calculated to be 5.3 for both the peanut and olive oil fumes. To quantify the newly produced PCNs, sucralose used in the experiments were about 2 or 3 orders of magnitude higher than in reality. PCNs were not detected with real proportions under the current experimental conditions. [Copyright &y& Elsevier]

Abstract: Several temperate freshwater eel stocks have experienced unsustainable declines, yet to be explained. The decline of lake trout (Salvelinus namaycush) in Lake Ontario has been linked to aryl-hydrocarbon receptor agonists such as polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs), dioxin-like polychlorinated biphenyls (dl-PCBs), and polychlorinated naphthalenes (PCNs), and the question remains whether eels are affected similarly by these compounds. Concentrations of PCDD/Fs, dl-PCBs, and PCNs were determined in eels collected at seven locations in eastern Canada including L. Ontario, one location in New York, USA, and one location in Flanders, Belgium. Concentrations varied greatly among origins, indicating dissimilar historic loadings to local areas. The risk to eel reproduction was evaluated with 2,3,7,8-TCDD toxic equivalents, and increased by 10-fold from the least to most contaminated site. The risk to eel recruitment from dioxin-like compounds in American eel using available guidelines is low. The development of a more comprehensive model for eel recruitment risk assessment due to dioxin-like compounds, using eel-specific guidelines, is recommended. Toxic equivalents were 5-fold higher when based on mammalian toxic equivalency factors compared to fish values. About half of the eels captured in L. Ontario exceeded the Canadian guideline for fish consumption (20pg TEQ g−1 ww), but there were no other exceedances in Canada. The current risk to eel consumers in Canada is low overall, except for highly urbanized and industrialized areas. [Copyright &y& Elsevier]

The use of passive air samplers (PAS) in recent years to monitor the occurrence of persistent organic pollutants (POPs) in air has been increasing, not only globally, but also at regional and/or local scales. The present study was aimed at analyzing the airborne concentrations of the POPs: polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), and polychlorinated naphthalenes (PCNs) in the vicinity of a municipal solid waste incinerator (MSWI) in Tarragona (Catalonia, Spain). Mean air levels of PCBs, PBDEs, and PCNs were 44.1, 65.0, and 6.65 pg/m3, respectively. No differences were noted according to the distance or direction from the plant for any chemical. Furthermore, this information was used to estimate the air inhalation of POPs for the local population. Environmental exposure to POPs through air accounted for only <2% of the total when compared with the dietary intake. The overall results indicate that the MSWI here assessed does not mean a relevant increase on human health risks derived from inhalation of POPs. PAS can also be utilized for human health risk assessment studies, being also suitable tools to control the environmental burden of non-regulated chemicals, for which no emission thresholds have yet been derived. [ABSTRACT FROM AUTHOR]

Nine typical waste incinerating plants were investigated for polychlorinated naphthalene (PCN) contents in their stack gas. The incinerators investigated include those used to incinerate municipal solid, aviation, medical, and hazardous wastes including those encountered in cement kilns. PCNs were qualified and quantified by isotope dilution high resolution gas chromatography-high resolution mass spectrometry techniques. An unexpectedly high concentration of PCNs (13,000 ng Nm) was found in the stack gas emitted from one waste incinerator. The PCN concentrations ranged from 97.6 to 874 ng Nm in the other waste incinerators. The PCN profiles were dominated by lower chlorinated homologues, with mono- to tetra-CNs being the main homologues present. Furthermore, the relationships between PCNs and other unintentional persistent organic pollutants involving polychlorinated dibenzo- p-dioxins and dibenzofurans, polychlorinated biphenyls, hexachlorobenzene, and pentachlorobenzene were examined to ascertain the closeness or otherwise of their formation mechanisms. A good correlation was observed between ΣPCN (tetra- to octa-CN) and ΣPCDF (tetra- to octa-CDF) concentrations suggesting that a close relationship may exist between their formation mechanisms. The results would provide an improved understanding of PCN emissions from waste incinerators. [ABSTRACT FROM AUTHOR]

The chlorination patterns of unsubstituted naphthalene were studied using a laminar flow reactor with a 1 cm particle bed of 0.5% (mass) copper(II) chloride (CuCl2) mixed with silicon dioxide (SiO2), operated over a temperature range of 100 to 400 °C and at gas velocities of 2.7 and 0.32 cm/s. The polychlorinated naphthalene (PCN) yield increased until a temperature reached at 250 °C, where a peak yield of 3.07% (percent of naphthalene input, carbon basis) was observed. All PCN homologue groups, mono- through octa-chlorinated naphthalenes, were observed. To test the hypothesis that PCNs in combustion processes are formed via chlorination pathways, the PCN homologue and isomer patterns from the experiments were compared with those observed in municipal solid waste combustion (MSW) incinerators. PCN congeners with 1,4-substituents dominated formation in the naphthalene chlorination experiments, whereas 2,3-substituents were major congeners in both MSW combustion flue gas and fly ash samples. These results suggest that contrary to the hypothesis, chlorination is not a primary PCN formation route in either the flue gas or fly ash from MSW combustion. Even so, naphthalene chlorination pathways presented in this paper provide an improved means for evaluating PCN formation mechanisms in combustion processes. [ABSTRACT FROM AUTHOR]

A method for the selective separation of polychlorinated naphthalene (PCNs), hexabromocyclododecanes (HBCDs) and tetrabromobisphenol A (TBBPA) in complex matrices was developed. In the present study, the type of sorbents and the volume and composition of eluting solvents were investigated in detail. Under the optimal conditions, the recoveries of PCNs, HBCDs and TBBPA in different fractions were determined with liquid/gas chromatography tandem mass spectrometry (LC or GC-MS/MS), which was nearly close to 100%. To investigate the feasibility of the developed method, it was applied to isolate target compounds from spiked soil extracts. PCNs, HBCDs and TBBPA could be subsequently eluted with hexane, hexane/dichloromethane (1:1), and hexane/dichloromethane (1:3), and the recoveries of the analysts from three fractions were satisfactory (70.9%-107%) with the exception of γ-HBCD at low levels. The results indicated that the method exhibited good performance for the selective separation of PCNs, HBCDs and TBBPA and showed great potential in sample pretreatment in terms of alleviating influence from different class of impurities to some extent. [ABSTRACT FROM AUTHOR]

Abstract: Topsoil along the altitudinal gradient (2086–4487m above sea level) and yak samples, collected from Wolong high mountain area of Sichuan Province, western China, were analyzed for polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs), dioxin-like polychlorinated biphenyls (dl-PCBs) and polychlorinated naphthalenes (PCNs) using HRGC–HRMS. The total concentrations of PCDD/Fs, dl-PCBs, and PCNs in soils were: 2.48–4.30pgg−1 dw (dry weight), 7.6–10.5pgg−1 dw, and 13.0–29.0pgg−1 dw, respectively; the greatest concentrations were found at sampling sites of 3927m, 4487m and 3345m, correspondingly. The total PCDD/Fs and dl-PCBs concentrations showed positive correlations with increasing altitudinal gradient. The congener profiles of both 2,3,7,8-PCDD/Fs and dl-PCBs at different altitudes showed similar patterns. PCNs were dominated by Tri-CNs. The long-range atmospheric transport and subsequent aerial deposition are likely the sources for these POPs in area examined. The total TEQs in soils were in the range of 0.28–0.42pgg−1 dw, and the total TEQs in the yak muscle and fatty tissue samples were 3.81–4.09pgTEQg−1 lipid weight. The daily intake of TEQs was estimated to be below the WHO''s tolerable daily intake according to the local people''s dietary habits in Wolong area, which is unlikely to cause any adverse health effects to the yak muscle consuming people. [Copyright &y& Elsevier]

Polychlorinated naphthalenes (PCNs) are a group of organochlorinated compounds exhibiting dioxin-like properties. Previously published data showed the direct action of PCN-rich Halowax 1051 on ovarian follicular steroidogenesis. Taking into consideration that the observed biological effects of PCNs may be frequently side effects of metabolites generated by their detoxification, the aim of this study was to determine the activity and expression of enzymes involved in phase I (cytochrome P450, family 1 (CYP1A1)) and phase II (sulfotransferase (SULT1A) and catechol-O-methyltransferase (COMT)) detoxification metabolism. Cocultures of granulosa and theca interna cells collected from sexually mature pigs were exposed to 1 pg/mL to 10 ng/mL of Halowax 1051 for 1 to 48 hours, after which levels and activities of CYP1A1, SULT1A, and COMT were measured. Dose-dependent increases of CYP1A1 activity and expression were observed. High doses of Halowax 1051 were inhibitory to COMT and SULT1A activity and reduced their protein levels. In conclusion, fast activation of phase I enzymes with simultaneous inhibition of phase II enzymes indicates that the previously observed effect of Halowax 1051 on follicular steroidogenesis may partially result from metabolite action occurring locally in ovarian follicles. [ABSTRACT FROM AUTHOR]

Organohalogen chemicals of emerging concern (CECs) have attracted much attention during the past decade and are of special importance for the Great Lakes of North America, which are together the largest surface freshwater resource on the earth. In this paper we review and summarize detection and levels of legacy contaminants in Great Lakes fish, lessons learned from legacy contaminants in advancing the analytical detection of CECs, progress and challenges in measuring CECs, and levels of CECs in Great Lakes fish reported to date. The CECs considered include chlorinated paraffins, polychlorinated naphthalenes and other chlorinated aromatics, halogenated flame retardants, and perfluorinated compounds. [ABSTRACT FROM AUTHOR]

The concentrations of polychlorinated dibenzo- p-dioxins/dibenzofurans (PCDD/Fs), dioxin-like polychlorinated biphenyls (PCBs), and polychlorinated naphthalenes (PCNs) were measured in two sediment cores collected from Jiaozhou Bay. The concentrations of PCDD/Fs, dioxin-like PCBs, and PCNs in the cores were in the range of 2.8-26.3, 7.1-82.4 and 3.9-56.4 pg/g dw, respectively. The depth profiles of total concentrations PCDD/Fs and dioxin-like PCBs were similar in the sediment core J37 inside Jiaozhou Bay, but different from those in the sediment core J94 outside the bay, suggesting the different sources. In both cores Tri-CNs and Tetra-CNs were dominant, similar to the PCNs composition of some Halowax technical products. The maximal PCNs contamination occurred in the mid-1970s (outside the Bay) and early-1990s (inside the Bay). An increase of the indicator CN congeners characteristic for thermal source in the top layers of the sediment core inside the bay indicated that the contribution from the municipal solid waste incineration has been more important in recent years. [ABSTRACT FROM AUTHOR]

Polychlorinated naphthalenes (PCNs) are now under review by the Stockholm Convention as a candidate for POPs for their persistence, toxicity, bioaccumulation, and long-range atmospheric transport. Data regarding PCN levels and their environmental fate are sparse in China. The PCN concentration and distribution in soils of the Pearl River Delta were reported, and the average total concentration was 59.9 ± 86.7 pg/g. Tri-CNs was the dominant homologue group, and CN 24 was the most abundant congener. A gradient of PCN levels between more and less developed areas was observed. Based on fugacity fraction results, CN 51 is proposed as a possible source marker for specific combustion emissions. Air-soil exchange of PCNs was estimated by calculating the soil and air fugacity. Fugacity fraction values indicated that tri- to penta-CNs were closer to equilibrium in winter and toward net volatilization in summer, while hexa-CNs experienced net air-to-soil transfer in both seasons. [Copyright &y& Elsevier]

Abstract: Iron ore sintering processes constitute significant sources of dioxins, and studies have confirmed a close correlation between polychlorinated naphthalenes (PCNs) and dioxin formation. Thus, iron ore sintering processes are thought to be a potential source of PCNs, although intensive investigations on PCN emissions from sintering processes have not been carried out. Therefore, the aim of the present study was to qualify and quantify PCN emissions from nine sintering plants operating on different industrial scales. PCN concentrations ranged from 3 to 983ngm−3 (0.4–23.3pgTEQPCN m−3) and emission factors ranged from 14 to 1749μgt−1 (0.5–41.5ngTEQPCN t−1), with a geometric mean of 84μgt−1 (2.1ngTEQPCN t−1). The estimated annual emission of PCNs from sintering processes in China was 1390mg TEQPCN. These figures will assist in the development of a PCN emissions inventory. Regarding emission characteristics, PCNs mainly comprised low-chlorinated homologs. The ratios of several characteristic PCN congeners were also measured and compared with those from other sources. Taken together, these results may provide useful information for identifying the sources of PCNs produced by iron ore sintering processes. [Copyright &y& Elsevier]

Abstract: Field monitoring was conducted to update and develop unintentional persistent organic pollutant (unintentional POP) emission inventories for the copper metallurgy industry in China. In this study, emissions of six unintentional POPs comprised of polychlorinated dibenzo-p-dioxin and dibenzofuran (PCDD/PCDF), polychlorinated biphenyls (PCBs), polychlorinated naphthalenes (PCNs), hexachlorobenzene (HxCBz) and pentachlorobenzene (PeCBz) in stack gas and fly ash samples from primary and secondary copper smelters using different raw materials and technologies were measured and compared. Different concentrations, congener patterns and emission factors of unintentional POPs among four copper smelters were observed. Variations in unintentional POP emissions from several areas of a primary copper smelter were also investigated. The total emissions of unintentional POPs from primary and secondary copper production in 2010 in China were estimated respectively. These results provide a useful reference for the establishment of unintentional POP emission inventories and for policymakers to formulate control strategies to reduce unintentional POPs resulting from copper metallurgy. [Copyright &y& Elsevier]

Abstract: Monitoring marine persistent organic pollutants (POPs) is important because oceans play a significant role in the cycling of POPs. The South China Sea (SCS) is surrounded by developing countries in Southeast Asia which are centers of e-waste recycling and the ship dismantling industry. In this study, shipboard air samples collected over the SCS between September 6 and 22, 2005 were analyzed for polychlorinated biphenyls (PCBs) and polychlorinated naphthalenes (PCNs). The levels of ∑12PCBs ranged from 32.3 to 167pgm−3, with a mean value of 98.4±36.0pgm−3. Tetra-CBs were the predominant congeners. The concentrations of ∑18PCNs ranged from N.D. to 26.0pgm−3, with a mean value of 10.5±7.16pgm−3, and tri-CNs were predominant. The gaseous concentrations of PCBs and PCNs over the SCS were consistent with those over other seas and oceans. Compared with previous studies, it was found that the concentrations of PCBs exhibited an obviously declining trend. The measured PCB and PCN concentrations in the atmosphere over the SCS were influenced by their proximity to source regions and air mass origins. The highest gaseous PCB and PCN concentrations were found at sampling sites adjacent to the continental South China. E-waste recycling, ship dismantling and combustion in South China and some Southeast Asian countries might contribute PCBs and PCNs to the atmosphere of the SCS. [Copyright &y& Elsevier]

Electric arc furnaces (EAF) are well recognized as significant sources of dioxins. EAFs have also been speculated to be sources of polychlorinated naphthalenes (PCNs) due to the close correlation between dioxin and PCN formation. However, assessment on PCN emissions from EAFs has not been carried out. The primary aim of this preliminary study is to identify and characterize the atmospheric emission of PCNs from EAFs. In this preliminary study, stack gas samples from two typical EAFs with different scales (EAF-1, 160 t batch; and EAF-2, 60 t batch) were collected by automatic isokinetic sampling technique, and PCN congeners in samples were analyzed by isotope dilution high-resolution gas chromatography combined with high-resolution mass spectrometry method. Emission concentrations of PCNs were 458 and 1,099 ng m for EAF-1 and EAF-2, respectively. The emission factors of PCNs to air were 21.6 and 30.1 ng toxic equivalent t for EAF-1 and EAF-2, respectively, which suggested that EAF is an important source of PCN release. With regard to the characteristics of PCNs from EAFs, lower chlorinated homologues were dominant. The PCN congeners comprised of CN27/30, CN52/60, CN66/67, and CN73 were the most abundant congeners for tetra-, penta-, hexa-, and hepta-chlorinated homologues, respectively. EAFs were identified to be an important PCN source, and the obtained data are useful for developing a PCN inventory. The congener profiles of PCNs presented here might provide helpful information for identifying the specific sources of PCNs emitted from EAFs. [ABSTRACT FROM AUTHOR]

Abstract: This study measured organochlorine pesticides (OCPs) including hexachlorocyclohexanes (HCHs), hexachlorobenzene (HCB), heptachlor and dichlorodiphenyltrichloroethanes (DDTs), polychlorinated biphenyls (PCBs), polychlorinated naphthalenes (PCNs) and polybrominated diphenyl ethers (PBDEs) in tissues of six mother–fetus pairs of harbor seals that were hunted for subsistence in Alaska waters of the Northern Pacific Ocean. These data suggest that significant amounts of these contaminants were transferred from mother harbor seals to fetuses during pregnancy and distributed among fetal organs. The tissue distribution depended on the chemical groups, the specific compounds in the groups and the target organs. Concentration profiles of ∑OCPs, ∑PCBs, ∑PCNs and ∑PBDEs were remarkably similar among maternal blubber, liver, and placenta, fetal blubber, and liver (except for HCHs), possibly indicating that the placenta did not serve as a barrier for all of the compounds analyzed. DDTs, HCB, HCHs, PCBs and PBDEs could penetrate the placenta and accumulate in the blubber of the fetus in utero, while HCHs, PCBs and PBDEs penetrated the placenta and accumulated more preferentially in the fetal liver than in the fetal brain in comparison with DDTs and HCB. Heptachlor and PCNs penetrated the placenta and accumulated in the fetal liver and brain instead of fetal blubber. Similar maternal transfer trends for OCPs, PCBs, PCNs and PBDEs were shown by fetal to maternal (FM) blubber ratios and FM liver ratios. Prenatal transfer of these toxic contaminants from mothers to fetus presumably through the placenta may pose health risks to the fetus during early development. [Copyright &y& Elsevier]

Abstract: An improved correction method was established using passive air samplers to assess the distributions of polychlorinated naphthalenes (PCNs) in the eastern Pearl River Delta, South China. This method was based on a joint correction that used the active air sampling rate and the addition of depuration compounds. As a correction factor, the depuration compounds’ properties do not need to be similar to the target compounds. The total PCN air concentrations ranged from 6.4 to 832, with an average of 148±201pgm−3 in the study area, while the TEQ of the PCNs ranged from 1.2×10−4 to 2.6×10−2 pgm−3. High concentrations of PCNs were mostly observed in the highly industrialized areas. The PCN air levels were remarkably increased in winter compared with summer. Tri-CNs was the most dominant homologue group, while CN 24 was the most dominant congener. The high proportion of combustion-related PCNs suggests that the contribution of combustion sources to the PCN air burden has been significant recently in comparison with historical emissions. [Copyright &y& Elsevier]

Abstract: Polychlorinated naphthalenes (PCNs), including hexachloronaphthalene (HxCN), are widespread global environmental contaminants. Our experiments were aimed at assessing HxCN effects on motor behavior, long-term memory, pain sensitivity, magnitude of stress-induced analgesia, auditory function and sensorimotor gating, following repeated intragastric administration (28 days) of HxCN at 0.3 and 1.0mg/kg body weight. Three weeks after the exposure termination, male Wistar rats were subjected to the neurobehavioral tests battery performed in the following order: open-field test, passive avoidance test, hot-plate test and acoustic startle response test. Repeated administration of HxCN induced disorders of motivational processes manifested by: anorectic effect caused by aphagia and adipsia; significantly reduced motor activity (hypokinesia); impaired long-term memory and acquired passive avoidance reaction; reduced pain threshold and shortened duration of anxiety reaction after pain stimulus (sensory neglect). Some of these neurobehavioral effects (impaired long-term memory, reduced pain threshold and stress-induced analgesia) were observed at 0.3mgHxCN/kg body weight without any signs of overt toxicity. The outcome of our study shows that HxCN, like other compounds of the persistent organic pollutants (POPs) group, creates a potential risk of behavioral changes in the central nervous system in the general population as a result of environmental exposure. [Copyright &y& Elsevier]

Objectives: Polychlorinated naphthalenes (PCNs), like other persistent organic pollutants (POPs), are widespread, global environmental contaminants. These compounds still represent a great environmental problem, mostly because of the risk of secondary air pollution. They are characterized by long durability and tendency to bioaccumulate, which means that they are practically ubiquitous in all environmental media and ecosystems. The aim of this study was to investigate the distribution and excretion of hexachloronaphthalene (HxCN) in rats following a single intraperitoneal or intragastrical administration. Materials and Methods: Experiments were performed on male outbred Wistar rats with body weight of 220-240 g. They were given [C]-HxCN intraperitoneally (i.p.) or intragastrically (p.o.) in a single dose of 0.3 mg (150 kBq) per rat. The distribution of radioactivity in blood and selected organs or tissues, as well as urine and faeces excretion were traced following the administration. Results: The decline of [C]-HxCN in plasma was biphasic and the calculated half-lives for phases I and II were ∼6 and 350 h, respectively. Following 120 h after administration, ∼51% (intragastrical) and ∼34% (intraperitoneal) of the dose were excreted with faeces. Regardless of the administration route, the highest HxCN concentrations were found in liver and adipose tissue, where the compound showed high retention: the highest retention in liver was found 24 h after intragastrical (32%) and intraperitoneal (38%) administration while in adipose tissue ∼30% retention was observed 120 h after HxCN administration regardless of its route. Conclusions: Following the calculation of the balance of total [C]-HxCN excreted and stored, it was found that hexachloronaphthalene belongs to the compounds of a slow turnover rate, and in the case of repeated exposure it may accumulate in the rat body. [ABSTRACT FROM AUTHOR]

A selection of PCN congeners was analyzed in pooled blubber samples of pilot whale (Globicephala melas), ringed seal (Phoca hispida), minke whale (Balaenoptera acutorostrata), fin whale (Balaenoptera physalus), harbour porpoise (Phocoena phocoena), hooded seal (Cystophora cristata) and Atlantic white-sided dolphin (Lagenorhynchus acutus), covering a time period of more than 20 years (1986–2009). A large geographical area of the North Atlantic and Arctic areas was covered. PCN congeners 48, 52, 53, 66 and 69 were found in the blubber samples between 0.03 and 5.9 ng/g lw. Also PCBs were analyzed in minke whales and fin whales from Iceland and the total PCN content accounted for 0.2% or less of the total non-planar PCB content. No statistically significant trend in contaminant levels could be established for the studied areas. However, in all species except minke whales caught off Norway the lowest ∑PCN concentrations were found in samples from the latest sampling period. [Copyright &y& Elsevier]

A nationwide monitoring of atmospheric POPs (persistent organic pollutants) was conducted in Ghana between May and July 2010, applying polyurethane foam (PUF) disk passive air samplers (PAS). Reported here are preliminary findings on PCNs, an industrial organic contaminant currently under review for possible listing under the global chemical treaty. The present results constitute the first set of nationwide data on air PCNs from a West African country. Contrary to expectation, air PCNs levels were quite high in Ghana, at an average of 49 ± 5.4 pg/m³. The coastal (southern) zone of Ghana appeared the most impacted, with crude open burning of waste, industrial emissions, and the harbor environment identified among possible emission factors. Tri- and tetra-CNs (the lowly chlorinated homologues) predominated in the atmosphere, altogether constituting approximately 90% of total PCN homologues composition. Increased volatilization under tropical conditions was presumed a key factor that contributed to this high atmospheric input of lowly chlorinated homologues. We further observed a significant level of fractionation of PCN homologues across the breadth of the country. The percentage composition of the lowly chlorinated homologues increased northwards, probably because of their transportation in the direction of prevailing winds. From congener profile analysis, PCN-45/36 is proposed as a possible source marker for emissions preempted by uncontrolled waste burning activities. Dioxin-like toxicity of air PCNs in Ghana was estimated to range 0.49-5.6 fg TEQ/m³. This study brought to the fore the emerging problems of nonagricultural organohalogens that covertly might be confronting the environment in African nations like Ghana. [ABSTRACT FROM AUTHOR]

Abstract: A comprehensive congener specific evaluation of polychlorinated biphenyls (PCBs) and polychlorinated naphthalenes (PCNs) in the atmosphere was conducted across East Asia in spring 2008, applying polyurethane foam (PUF) disk passive air sampler (PAS) as monitoring device. Mean concentrations derived for Japan, China and Korea were 184±24, 1100±118, and 156±20pgm−3 for ∑202 PCBs, and 9.5±1.5, 61±6, and 16±2.4pgm−3 for ∑63 PCNs, respectively. Relative to reported data from 2004, the present results suggest that air PCBs concentrations have not changed much in Japan and Korea, while it has increased by one order of magnitude in China. From principal component analysis, combustion emerged highly culpable in contemporary emissions of both PCBs and PCNs across the East Asian sub-region. Another factor derived as important to air PCBs was re-emissions/volatilization. Signals from PCBs formulations were also picked, but their general importance was virtually consigned to the re-emissions/volatilization tendencies. On the contrary, counterpart PCNs formulations did not appear to contribute much to air PCNs. [Copyright &y& Elsevier]

Abstract: Oregon''s Senate Bill 737, enacted in 2007, required the state''s 52 largest municipal wastewater treatment plants (WWTP) and water pollution control facilities (WPCF) to collect effluent samples in 2010 and analyze them for persistent organic pollutants. These facilities are located state-wide and represent a variety of treatment types, service population sizes, geographic areas, and flow conditions. Of the 406 chemicals ultimately analyzed, 114 were detected above the level of quantification (LOQ) in at least one sample. Few persistent pollutants were found possibly because of their diversion from effluent via sorption to sludge (solids phase) or high LOQs for certain chemicals. Several pesticides, as well as benzene and phenol degradation products, all previously unreported in effluent, were detected. Ten polychlorinated biphenyls (PCB) congeners were present at low concentrations in ≤10 samples, while polychlorinated naphthalenes and dioxins/furans were not detected at all. Twenty-one polybrominated diphenyl ether (PBDE) congeners were found, nine of which have been reported in Osprey eggs in Oregon and Washington. Methylmercury was present in 65% of samples, with average and maximum concentrations of 0.18 and 1.36ng/L, respectively. Although they are generally assumed to be innocuous by-products of sewage treatment, additional research is needed on potential impacts to aquatic ecosystems of high loadings of coprostanol and cholesterol. These results suggest that effluent, rather than just receiving waters, should itself be analyzed for a wide range of contaminants in order to understand how upstream sources, conveyed through WWTPs and WPCFs, could be impacting aquatic ecosystems. [Copyright &y& Elsevier]

Polychlorinated naphthalenes (PCNs) are dioxin-like environmental contaminants. There is growing concern over the endocrine-disrupting effects of PCNs, but very few studies have investigated the effect of PCNs on the thyroid system. This study used a yeast two-hybrid assay, which included the recombinant human thyroid receptor(TR)-β and reporter genes, to characterize the TRβ-disrupting effects of five individual PCN congeners, five PCN Halowax mixtures, and naphthalene. Their agonist and antagonist effects were studied in the absence and presence of 5x10-7 mol/L 3,3',5-triiodo-L-thyronine, which induced submaximal β-galactosidase activity. Naphthalene, 1,2,3,4,5,6,7,8-octachloronaphthalene and all of the Halowax mixtures (Halowax 1000, 1001, 1013, 1014 and 1099) showed no agonist or antagonist activity on TRβ at the concentrations tested (up to 10-2 g/L). The lighter PCN congeners, namely 1-chloronaphthalene, 2-chloronaphthalene, 1,4-dichloronaphthalene and 1,2,3,4-tetrachloronaphthalene showed no agonist activity but showed significant antagonist activity on TRβ. The 20% relative inhibitory concentrations of these PCNs were less than 9.13 x 10-3 g/L. Thus, bioaccumulation of these lighter PCN congeners may disrupt the thyroid hormone system and inhibit TR-mediated cellular responses. Studies in the future should investigate the possible associations between the presence PCNs and adverse health outcomes. [ABSTRACT FROM AUTHOR]

Abstract: A broad spectrum of organic chemicals is essential to modern society. Once discharged from industrial, domestic and urban sources into the urban wastewater collection system they may transfer to the residual solids during wastewater treatment and assessment of their significance and implications for beneficial recycling of the treated sewage sludge biosolids is required. Research on organic contaminants (OCs) in biosolids has been undertaken for over thirty years and the increasing body of evidence demonstrates that the majority of compounds studied do not place human health at risk when biosolids are recycled to farmland. However, there are 143,000 chemicals registered in the European Union for industrial use and all could be potentially found in biosolids. Therefore, a literature review of ‘emerging’ OCs in biosolids has been conducted for a selection of chemicals of potential concern for land application based upon human toxicity, evidence of adverse effects on the environment and endocrine disruption. To identify monitoring and research priorities the selected chemicals were ranked using an assessment matrix approach. Compounds were evaluated based upon environmental persistence, human toxicity, evidence of bioaccumulation in humans and the environment, evidence of ecotoxicity and the number and quality of studies focussed on the contaminant internationally. The identified chemicals of concern were ranked in decreasing order of priority: perfluorinated chemicals (PFOS, PFOA); polychlorinated alkanes (PCAs), polychlorinated naphthalenes (PCNs); organotins (OTs), polybrominated diphenyl ethers (PBDEs), triclosan (TCS), triclocarban (TCC); benzothiazoles; antibiotics and pharmaceuticals; synthetic musks; bisphenol A, quaternary ammonium compounds (QACs), steroids; phthalate acid esters (PAEs) and polydimethylsiloxanes (PDMSs). A number of issues were identified and recommendations for the prioritisation of further research and monitoring of ''emerging'' OCs for the agricultural use of biosolids are provided. In particular, a number of ‘emerging’ OCs (PFOS, PFOA and PCAs) were identified for priority attention that are environmentally persistent and potentially toxic with unique chemical properties, or are present in large concentrations in sludge, that make it theoretically possible for them to enter human and ecological food-chains from biosolids-amended soil. [Copyright &y& Elsevier]

Abstract: Polychlorinated naphthalenes (PCNs) consist of naphthalene substituted with 1–8 chlorines, yielding 75 possible congeners. They were formerly used in industry, occur at trace levels in commercial PCB mixtures, and have current sources in combustion processes. PCNs are widespread in arctic air with higher levels in the European Arctic. Concentrations were higher during the cold months in arctic Canada and Russia, but no seasonality was noted in subarctic Canada and Greenland. “Marker” congeners indicative of combustion were evident at some sites. Total toxic equivalents (TEQ) in air due to PCNs+dioxin-like PCBs were dominated by PCNs in arctic Canada and Russia, but not in subarctic Canada. Deposition of PCNs in snow was measured in northern Norway and Svalbard. Surveys of PCNs in the lower food web are limited to the northern Baltic Sea and lakes/rivers of northern Scandinavia. PCNs showed little or no biomagnification in lower food webs of the northern Baltic and discrimination among congeners suggested preferential metabolism. There are no reports of PCNs in fish and invertebrates from the Arctic Ocean, and only one from Antarctica. Total PCNs in marine mammals followed the order: harbour seal~pilot whale≥polarbear>beluga>ringed seal~Weddell seal. Total PCNs in seabirds varied over 100-fold, with higher concentrations in glaucous gull eggs and plasma from Bear Island, and livers of northern fulmar from the eastern Canadian Arctic. Lower concentrations occurred in eggs of glaucous gull from Svalbard and black-backed gull from the Faroe Islands. PCNs accounted for <1% of total TEQ in ringed seal, Weddell seal, seabirds and polar bear, but up to 6–15% in beluga and pilot whale. TEQ due to PCNs were generally low in harbour seal, but up to 9% of total TEQ in some animals. [Copyright &y& Elsevier]

Prior to this study, reports of occurrence of polycyclic musks and polychlorinated naphthalenes (PCNs) in human tissues from Italy were not available. In this study, concentrations of PCNs and polycyclic musks were determined in human adipose tissue from Italy collected during 2005–2006; for comparison, legacy organohalogen pollutants such as organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), and polybrominated diphenyl ethers (PBDEs) were determined. ΣPCN concentrations ranged from 0.5 to 14 ng/g lipid wt (lw). Polycyclic musks such as HHCB and AHTN were found in 92% and 83% of the human samples, respectively. Concentrations of PBDEs in Italian adipose tissue ranged between 3.2 and 35.6 ng/g lw. [Copyright &y& Elsevier]

Concentrations of polychlorinated naphthalenes (PCNs) were determined in archived lake trout (Salvelinus namaycush) from Lake Ontario, North America, collected between 1979 and 2004 to evaluate their temporal trends and the factors influencing their trends. Concentrations of PCNs, as well as polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), and non- and mono-ortho-substituted polychlorinated biphenyls (DL-PCBs), which were measured for comparative purposes, declined by eight-, seven-, and fivefold, respectively, between 1979 and 2004. Apparent elimination rate constants (κ2) were calculated as the slopes of the regression lines of concentration versus time for PCN, DL-PCB, and PCDD/F congeners to compare the rate of decrease among congeners within and between compound classes. The κ2 values for PCNs that had two pairs or three adjacent carbons unsubstituted with chlorine (congeners that can be biotransformed by vertebrates) were not significantly different from zero, indicating no decline in fish. For PCN congeners having no adjacent carbons unsubstituted with chlorine, the κ2 values generally increased with hydrophobicity and degree of chlorination. This pattern differed from that of PCDD/Fs and DL-PCBs and from previous findings for non-DL-PCBs, for which the rate of contaminant decline decreased with hydrophobicity, and the pattern also differed from expectations based on thermodynamics. Differences in the rate of decline of PCN congeners may be caused by changes in source or mixture formulations over time and/or metabolic dechlorination of the less stable, higher-chlorinated PCNs 73, 74, and 75 to lower-chlorinated congeners. Based on suggested dioxin toxic equivalency factors, PCN concentrations in these whole lake trout may be sufficient to trigger consumption restrictions in Ontario, Canada, and our results suggest that PCNs merit incorporation into monitoring and assessment programs. [ABSTRACT FROM AUTHOR]

Secondary copper smelting is an important industrial source of unintentionally produced persistent organic pollutants (UPOPs) emissions. Herein, field study on industrial-scale plants was conducted to clarify the levels and profiles of polychlorinated biphenyls (PCBs), polychlorinated naphthalenes (PCNs) and chlorinated polycyclic aromatic hydrocarbons (> 3 rings, Cl-PAHs) from secondary copper smelting plants. The three UPOPs emission levels from the oxygen-enriched smelting furnace were higher than that from the anode furnace, which was attributed to the low-grade raw materials used. The toxic equivalent quantity concentrations of Cl-PAHs were 1.3–4.4 and 4.6–18.9 times higher than that of PCBs and PCNs, respectively. Thus, the emission control of Cl-PAHs in the secondary copper industry should be of concern. The chlorination degree of PCBs and PCNs was ~4 after the gas-cooling stage but was reduced to 1–2 in the stack outlet. This result indicated that the PCBs and PCNs congeners that were generated during the cooling stage were mainly higher-chlorinated. After purification by air pollution control devices (APCDs), the high-chlorinated congeners were removed simultaneously with the fly ash, whereas the low-chlorinated congeners may be regenerated and transferred into the stack gas due to possible memory effect within the APCDs. [Display omitted] • PCBs, PCNs and chlorinated PAHs emitted from secondary copper smelting were studied. • PCBs and chlorinated PAHs contributed the most to the total TEQ concentration. • Memory effect possibly increased the concentration of UPOPs in the flue gas. • Variation of homologs in the flue gas from cooling stage to stack outlet was clarified. [ABSTRACT FROM AUTHOR]

Organic species in fine particulate matter (PM 2.5) may exhibit significant health risks. The level, composition and sources of PM 2.5 -bound organic pollutants are temporally and spatially highly variable. In this study, the pollution characteristics and health risks of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), polychlorinated naphthalenes (PCNs) and polychlorinated dibenzo-p-dioxins/furans (PCDD/Fs) in PM 2.5 of Dalian were investigated. PM 2.5 -bound organic pollutants in Dalian were generally lower than other regions in China and other countries, significant seasonal changes were observed, higher levels appeared in winter than in summer. Concentrations of 16 PAHs were 2.07 ng/m3 and 13.99 ng/m3 in summer and winter, respectively. PAHs with 4-ring and 5-ring were the dominant components. Diagnostic analysis and principal component analysis (PCA) indicated that PAHs mainly originate from petroleum emissions and combustion. Concentrations of PCDD/Fs, PCBs and PCNs in PM 2.5 ranged from 0.05 to 3.27, 0.04–0.65 and 0.05–1.42 pg/m3, respectively. PCDD/Fs and PCBs were mainly consisted of high-chlorinated homologues during the sampling period. High-chlorinated PCNs were dominated only in winter, while low-chlorinated PCNs were dominated in summer, industrial thermal activity was one of the main sources of PCNs. The high correlation coefficients of the concentration of PAHs, PCBs, PCNs, and PCDD/Fs with that of SO 2 indicated that combustion sources contributed more to PM 2.5 -bound organic pollutants than that of motor vehicle emissions. The incremental lifetime cancer risk induced by PM 2.5 -bound POPs is relatively lower in Dalian than other regions. [Display omitted] • Concentrations of PM 2.5 -bound POPs in Dalian exhibited obvious seasonal changes. • Source apportionment was performed using diagnostic analysis and PCA. • The ILCR induced by PM 2.5 -bound POPs is relatively low in Dalian. [ABSTRACT FROM AUTHOR]

Abstract: The aim of the study was to investigate the subacute toxicity of a polychlorinated naphthalene (PCN) mixture and its effect on cytochrome P-450 levels in rats. The animals were administered PCNs intragastrically in repeated daily doses of 1, 10, and 100mg/kg. The animals were dissected after 7, 14, or 21 doses. Doses of 10 and 100mg/kg induced a significant decrease in the body weight at all time points of the experiment compared with the control group. The exposure to PCNs increased both the level of total cytochrome P-450 and the activity of CYP 1A at the same time points. In the groups of rats given PCNs in doses of 10 and 100mg/kg, an evident dose- and time-dependent increase in malondialdehyde (MDA) level was observed throughout the experiment. The correlation between the increased MDA and decreased glutathione (GSH) levels in the liver was also observed. [Copyright &y& Elsevier]

Among polychlorinated naphthalenes (PCNs), listed by the Stockholm convention as Persistent Organic Pollutants (POPs), hexachloronaphthalenes are considered the most toxic and raise the highest concern. Of these, 1,2,3,5,6,7-hexachloronaphthalanene (PCN67) is considered the main congener affecting human health due to its hepatotoxicity and its ability to disturb the reproductive, endocrine, and hematological systems. It is also prevalent in human serum/plasma, milk, and adipose tissue. However, little is known about its neurotoxicity, despite the fact that anorectic effects have been observed in workers occupationally exposed to PCNs and in animal research on PCN67. Since dopamine is involved in many aspects of food intake, the aim of this study was to confirm whether PCN67 affects dopamine synthesis in differentiated PC12 cells, a widely used model of neurosecretion. Our results show that exposure to PCN67 resulted in diminished dopamine content and release. Moreover, PCN67 also affected the expression of tyrosine hydroxylase and lowered the expression of vesicular monoamine transporter 1 (VMAT1). In addition, significantly lower expression of antioxidant enzymes, including catalase, glutathione peroxidase and copper/zinc superoxide dismutase, was observed in comparison to the vehicle. In conclusion, PCN67 appears to disturb dopaminergic transmission by altering tyrosine hydroxylation, reducing VMAT1 expression and impairing antioxidant protection. Our study provides a potential mechanism for how PCN67 may cause dopamine deficiency and contribute to neuronal death by affecting cellular antioxidant potency; however, this conclusion requires further research. [Display omitted] • Effects of PCN67 on in vitro dopaminergic secretion were studied. • PCN67 significantly inhibits biosynthesis of dopamine in PC12 cells. • PCN67 significantly decreased expression of CAT, GPx and SOD in PC12 cells. [ABSTRACT FROM AUTHOR]

Spatial trends, partitioning behavior, and potential sources of polychlorinated naphthalenes (PCNs) in water-sediment system from the Yangtze River Delta (YRD) were investigated in this study. The total concentrations of 75 PCNs in water and sediment samples were 0.022–0.310 ng/L and 0.01–1.59 ng/g dry weight, respectively. The homolog patterns in the sediment and water samples were somewhat different. Di-to tetra-CNs made larger contributions in the sediment, while the mono-to tri-CNs were dominant homologs in the water. Overall, the low-chlorinated naphthalenes (mono-to tetra-CNs) were found to be the dominant homologs in the YRD water and sediment samples, and the homolog group contributions to the total PCNs concentrations decreased as the number of chlorine atoms increased. CN-5/7 and CN-24/14 were found at high concentrations in both the water and sediment. Partitioning and transfer of PCNs between water and sediment were assessed by calculating the partition coefficients and fugacity fractions. The partition coefficients showed that PCNs were not in equilibrium status in the water–sediment system, and hydrophobicity played an important role in PCNs partitioning. The fugacity fractions indicated that mono- to tri-CNs had stronger tendencies to escape from the sediment into the water, while the high-chlorinated naphthalenes close to equilibrium. Principal component analysis and correlation analysis indicated that industrial thermal processes and the use and disposal of products containing PCNs industrial products are sources of PCNs in the YRD water-sediment system. [Display omitted] • Spatial trends, partitioning behavior and sources of PCNs in YRD were investigated. • The mono-to tetra-CNs were the dominant PCNs in water and sediment. • Partitioning and transfer of PCNs were assessed by partition coefficient and fugacity fraction. • Lower chlorinated PCNs had a stronger tendency to escape from the sediment to the water. • Emissions of PCNs during industrial thermal processes were the major sources in YRD. [ABSTRACT FROM AUTHOR]

Contamination of Elbe River (Germany) sediments with dioxin-like toxicants was investigated following the 500-year flood (flood that statistically occurs once in 500 years) of 2002. It was hypothesized that large amounts of particulate matter from river beds and associated dioxin-like toxicants were mobilized and transported during this flood event. The investigation focused on polychlorinated naphthalenes (PCNs) that have not been determined previously in the Elbe River. The in vitro H4IIE-luc assay was used as an overall measure for toxicants capable of binding to the aryl hydrocarbon receptor (AhR). The assay was combined with congener-specific instrumental analyses and fractionation to quantify PCN contributions to total AhR-mediated activity relative to polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and polychlorinated biphenyls (PCBs). Penta- to octachloronaphthalene concentrations of 30 ng/kg dry weight up to 13 μg/kg dry weight were found in Elbe River sediments downstream of Bitterfeld. Concentrations of penta- to octachloronaphthalenes, however, were only approximately 3 μg/kg dry weight at a site in the vicinity of Bitterfeld, where a level of approximately 3 mg/kg dry weight was reported before the flood. Also, the congener pattern of PCNs at this site changed after the flood, and PCN patterns reported previously for Bitterfeld and assigned to chloralkali electrolysis with graphite electrodes could now be observed at the sites from downstream of Bitterfeld and Magdeburg. Whereas PCDD/Fs dominated the dioxin-like activity in the middle and lower Elbe River, PCNs contributed as much as 10% of the total AhR-mediated activity. The contribution of PCBs was less significant (maximum, 0.2%). Thus, in Elbe River sediments, PCNs should be considered as relevant contaminants and be included in future monitoring and risk assessment programs. [ABSTRACT FROM AUTHOR]

Polychlorinated naphthalenes (PCNs), short-chain chlorinated paraffins (SCCPs) and polychlorinated biphenyls (PCBs) were analysed in marine sediment samples collected from the coastal area of Barcelona (Spain) and near of a submarine emissary coming from a waste water treatment plant located at the mouth of the Besòs River (Barcelona). An integrated sample treatment based on Soxhlet extraction followed by a simple clean-up with Florisil and graphitized carbon cartridge was employed. Gas chromatography coupled to ion-trap tandem mass spectrometry (GC–MS/MS) and gas chromatography–mass spectrometry in electron capture negative ionization mode, were used for PCN and SCCP determinations, respectively, while for PCB analysis gas chromatography with electron capture detection (GC-ECD) was used. The method developed provided low limits of detection (0.001–0.003ngg−1 dry weight (dw) for PCNs, 1.8ngg−1 for SCCPs and 0.006–0.014ngg−1 dw for PCBs) and good run-to-run precisions (lower than RSD 8%) for the analysis of sediment samples. Concentration levels ranging from 0.17 to 3.27ngg−1 dw for PCNs, between 0.21 and 1.17μgg−1 dw for SCCPs, and from 2.33 to 44.00ngg−1 (dw) for PCBs, were found in the coastal sediments, while for samples collected near to the submarine emissary higher levels (from 2.02 to 6.56ngg−1 dw for PCNs, between 1.25 and 2.09μgg−1 dw for SCCPs and from 22.34 to 37.74ngg−1 dw for PCBs) were obtained. The results obtained provide new data about the occurrence of PCN and SCCP in the coastal area of Barcelona. [Copyright &y& Elsevier]

A combination of non-polar and shape selective columns in a comprehensive two-dimensional GC (GC × GC) system consisting of DB-5MS and LC-50 as the 1st and 2nd dimension columns was used to separate 22 tetrachloronaphthalene isomers. These columns enabled separation of all possible isomers of tetraCN found in the technical chloronaphthalene Halowax formulations into 18 peaks covering 15 single separated isomers and 7 co-eluting in triplicate (1,2,4,6-/1,2,4,7-/1,2,5,7-tetraCN; nos. 33/34/37) and in pairs (1,2,3,7-/1,2,4,5-tetraCN; nos. 30/32 as well as 1,3,5,8-/1,3,6,8-tetraCN; nos. 43/45). Twelve isomers of tetraCN resolved as single compounds by the GC x GC system used were found in Halowax 1001, 1013, 1014 and 1099 as well as in Equi-Halowax mixture. Three other tetraCNs that could be also resolved as single compounds were not detected in these materials, while the remaining 7 tetraCNs, which co-eluted, waits a further separation. The majority of constituents of the tetraCN homologue group of the Halowax formulations are isomers such as 1,4,5,8-(no. 46), 1,2,5,8-(no. 38), 1,2,4,8-tetraCN (no. 35), co-eluting 1,3,5,8-tetraCN (no. 43 in a pair nos. 43/45) and also co-eluting 1,2,4,6-/1,2,4,7-/1,2,5,7-tetraCN (nos. 33/34/37). The less abundant by amongst of tetraCNs in these mixtures are 1,4,6,7-(no. 47) and 1,3,5,7-tetraCN (no. 42). The remaining seven isomers, i.e., 1,2,3,4-(no. 27), 1,2,3,5-(no. 28), 1,2,3,6-(no. 29), 1,2,5,6-(no. 36), 1,2,6,7-(no. 39), 1,2,6,8-(no. 40) and 1,2,7,8-tetraCN (no. 41) are usually minor by quantity, while 1,2,3,7-/1,2,4,5-tetraCN (nos. 30/32) are also minor, or one of them is absent. Three tetraCNs not found in the Halowax formulations are isomers such as 1,2,3,8-tetraCN (no. 31), 1,3,6,7-tetraCN (no. 44) and 2,3,6,7-tetraCN (no. 48). [ABSTRACT FROM AUTHOR]

This study determined the concentrations of organochlorine contaminants in common seafood in two Chinese coastal cities (Guangzhou and Zhoushan), and assessed the health risk due to the daily consumption of contaminated seafood. Twenty-six pooled samples, belonging to five food categories (fish, bivalves, shrimp, crab, and cephalopods), were purchased from local markets in Guangzhou and Zhoushan in 2003 and 2004. These samples were analyzed for total polychlorinated biphenyls (PCBs), non-and mono-ortho-PCBs (coplanar PCBs), polychlorinated naphthalenes (PCNs), and polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDDs/DFs). The concentrations of total PCBs and coplanar PCBs in fish samples were higher in Guangzhou than in Zhoushan, while the levels of PCNs and PCDDs/DFs were comparable between the two cities. The total daily intake values of dioxin-like compounds were 1.05 and 0.86pg WHO-TEQ/kg body weight in Guangzhou and Zhoushan, respectively. Hazard ratios of non-cancer risk in the two cities were all less than unity. [Copyright &y& Elsevier]