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Biomedical subjects

Michael G Ikonomou

Publications and source records attributed to Michael G Ikonomou.

At least 19 recordsLinked to original sources

An assessment of estrogenic organic contaminants in Canadian wastewaters.

A suite of 30 primarily estrogenic organic wastewater contaminants was measured in several influent/effluent wastewater samples from four municipal wastewater treatment plants and effluents from one bleached kraft pulp mill (BKME) using an ultra-trace analytical method based on gas chromatography-high resolution mass spectroscopy (GC-HRMS). In vitro recombinant yeast assay detection of the estrogenic equivalent (EEq) on whole and solid phase extracted (SPE) and fractionated wastewater was also performed. 19-norethindrone was the most frequently detected and abundant (26-224 ng/L) of all the synthetic estrogens/progesterones in the influent samples. 17alpha-ethinylestradiol was the more frequently detected synthetic estrogen/progesterone in the effluents occurring at or below 5 ng/L with some sporadic occurrences of up to 178 ng/L. The greatest levels of steroidal estrogens in municipal effluents were E1>E2>E3 which were all <20 ng/L. Nonylphenol and di(2-ethylhexyl) phthalate were found to be the highest non-steroidal synthetic compounds surveyed in both municipal influent and effluent samples, both occurring at 6-7 microg/L in municipal effluents. BKME contained relatively large amounts of the plant sterol stigmasterol (4 microg/L) but low amounts of fecal sterols, and steroidal estrogens (E2 only at 6 ng/L) when compared to the municipal effluents. In vitro EEq in the wastewater surveyed ranged from 9-106 ng E2/L and ranked from municipal influent>municipal effluent approximately BKME, with most of the estrogenicity fractionating in the 100% methanol SPE fraction followed by a secondary amount in the diethyl ether (for municipal) or methyl-tert butyl ether (for BKME) SPE fractions. Most correlations between chemical and in vitro estrogenic equivalency were weak (p>0.05 in most cases). Unexpected inverse correlations between in vitro estrogenic activity and concentrations of the estrogenic contaminant bisphenol A were found which likely contributed to the weakness of these correlations. A modified toxicity identification and evaluation procedure was continued with the SPE extracts from the more potent 100% methanol SPE fractions of municipal effluent. High performance liquid chromatography band elution retention times, based on in vitro estrogen detection, indicated that steroidal estrogens such as E2 were responsible for most of the estrogenicity of the samples. Subsequent collection and GC-MS analysis of active bands did not confirm the presence of steroidal estrogens, but expanded the possibility of phthalate esters (i.e. dibutyl phthalate) and natural sterols (i.e. beta-sitosterol) contributing to the overall estrogenic load.

Benzhydryl Compounds↗

Ion-trap tandem mass spectrometry-based analytical methodology for the determination of polychlorinated biphenyls in fish and shellfish. Performance comparison against electron-capture detection and high-resolution mass spectrometry detection.

Optimization of the Varian Saturn 2200 ion-trap tandem mass spectrometry (IT-MS/MS) system and comparison of its data quality with two other detection methods [electron-capture detection (ECD) and high-resolution mass spectrometry (HRMS)] was pursued by measuring polychlorinated biphenyls (PCBs) levels in fish and shellfish samples. IT-MS/MS methodology provided limits of detection (LOD) comparable to those obtained by ECD but superior specificity for the detection of a selected number of 39 PCB native congeners and 9 (13)C-labelled PCB standards. The method detection limits (MDLs) established for IT-MS/MS ranged between 1.0 and 5.0 pg/g on a wet weight basis while those obtained by ECD and HRMS were 1.0-4.0 pg/g and 0.1-2.0 pg/g, respectively. Overall, the results obtained in the study demonstrate that gas chromatography (GC) combined with IT-MS/MS provide higher data quality than those achievable by GC-ECD. For this particular set of target analytes the specificity achievable with IT-MS/MS was comparable to that obtained by HRMS and both techniques provided comparable data in terms of accuracy and precision.

Animals↗

Polybrominated diphenyl ethers in blood from Korean incinerator workers and general population.

This study was conducted to examine PBDE exposure in Koreans, with a special focus on incinerator workers due to their potential for occupational exposure to PBDEs. A total of 92 blood samples from 30 incinerator workers, 51 nearby residents and 11 controls were analyzed. The mean total PBDE concentration calculated from the 13 most concentrated congeners for all samples was 16.84+/-7.48 ng/g lipid, which was somewhat higher concentration than in other countries except North America and Canada. The PBDE levels and congener profiles detected in incinerator workers were not distinctly different from those found in the general population. In all groups tested, BDE-47 was dominant (mean contribution=32.5%) followed by BDE-153 (23.6%) and relatively high portions of BDE-183 (16.5%) were found. No strong trend was observed between PBDE levels and a number of key biological factors examined in this study, however, weak correlations were observed in PBDE levels measured against dietary habits, particularly in fish consumption frequency and gender. Overall, our data suggest that the occupational exposure of incinerator workers to PBDEs can be considered minor, while other lifestyle factors can have a greater contribution to PBDE exposure.

Adult↗

Sorption of phthalate esters and PCBs in a marine ecosystem.

Dialkyl phthalate esters (DPEs) are widely used industrial chemicals with octanol-seawater partition coefficients ranging between 10(1.80) for dimethyl phthalate to 10(10.0) for diiso-decyl phthalate, indicating a propensity to sorb strongly to particulate matter in aquatic environments. Sorption plays a key role in controlling the long-term fate of DPEs in aquatic systems and exposure to organisms in aquatic food-webs. However, field observations of the sorption of many commercial DPEs do not exist. To characterize the sorptive nature of DPEs in a real-world aquatic ecosystem, we measured concentrations of DPEs congeners, commercial DPE mixtures, and 10 polychlorinated biphenyls (PCBs) in water, suspended sediments, and bottom sediments of a marine inlet. Sorption coefficients of spiked and native DPEs and PCBs between suspended sediments and water indicate that the apparent sorptive nature of DPEs and PCBs is substantially greater than expected from K(ow)-based sorption models. Particulate and dissolved organic matter showed similar (i.e., not statistically different) sorption affinities for native analytes. The apparent fraction of the total aqueous concentration of DPEs that is freely dissolved and absorbable via the respiratory tract of aquatic organisms varied from virtually 100% for DMP to 0.0003% for C10. The observed decline in concentration of most DPEs between suspended and bottom sediments, compared to an increase in the concentration of high Kow PCBs, suggests that the rate of desorption and degradation of DPEs exceeds that of organic carbon mineralization and contributes to the previously observed lack of biomagnification of DPEs in the aquatic food-web of this system.

Ecosystem↗

Spatio-temporal and species-specific variation in PBDE levels/patterns in British Columbia's coastal waters.

Congener-specific levels of PBDEs were measured in the livers and some muscle tissues of Dungeness crab (Cancer magister), English sole (Pleuronectes vetulus) and spiny dogfish (Squalus acanthias). Highest concentrations (1,200-560 ng/g lipid) were found in crab collected near heavily urbanized areas (pop. approximately 0.3-1.8 million), followed by moderate levels at pulp/paper mills sites ( approximately 150 ng/g), and lowest levels occurred in areas that were somewhat removed from industrial/populated areas (< 24 ng/g). Temporal increases in total PBDEs and particularly in BDE-47 for Dungeness crab collected near pulp and paper and urbanized areas between 1994 and 2000 were observed. These correspond to Canadian and worldwide trends seen for PBDEs in biota. English sole and dogfish showed a pattern similar to that of the Columbia River whitefish samples, which corresponded closely to the patterns in the "penta" commercial mixture. Conversely, Dungeness crab were enriched in lower chlorinated PBDEs, particularly BDE-47 and BDE-49, compared to the fish and shark species from BC.

Animals↗

Polychlorinated dioxins and furans from the World Trade Center attacks in exterior window films from lower Manhattan in New York City.

Samples of ambient organic films deposited on exterior window surfaces from lower Manhattan and Brooklyn in New York City were collected six weeks after the terrorist attacks at the World Trade Center (WTC) on September 11, 2001 and analyzed for polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). Total tetra- through octa-CDD/F concentrations in window films within 1 km of the WTC site in lower Manhattan ranged up to 630,000 pg/m2 (estimated as a mass concentration of ca. 1,300,000 pg/ g) and a maximum toxic equivalent (TEQ) concentration of 4700 TEQ/m2 (ca. 10 000 pg TEQ/g). Measurements at a background site 3.5 km away in Brooklyn showed lower concentrations at 130 pg TEQ/m2 (260 pg TEQ/g). Ambient gas-phase PCDD/F concentrations estimated for each site using an equilibrium partitioning model suggested concentrations ranging from ca. 2700 fg-TEQ/m3 near the WTC site to the more typical urban concentration of 20 fg-TEQ/m3 atthe Brooklyn site. Multivariate analyses of 2,3,7,8-substitued congeners and homologue group profiles suggested unique patterns in films near the WTC site compared to that observed at background sites in the study area and in other literature-derived combustion source profiles. Homologue profiles near the WTC site were dominated by tetra-, penta-, and Hexa-CDD/Fs, and 2,3,7,8-substituted profiles contained mostly octa- and hexachlorinated congeners. In comparison, profiles in Brooklyn and near mid-Manhattan exhibited congener and homologue patterns comprised mainly of hepta- and octa-CDDs, similar to that commonly reported in background air and soil.

Air Pollutants↗

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.

Adult↗

Polychlorinated biphenyls, dioxins, and furans in weaned, free-ranging northern elephant seal pups from central California, USA.

The aim of this study was to measure persistent organic pollutants in northern elephant seals ([NES], Mirounga angustirotris). We obtained blubber biopsy samples from six healthy, newly weaned NES pups from Año Nuevo, California (USA). Contaminant levels were lower than those of other pinnipeds studied on the west coast of North America. Blubber concentrations of polychlorinated biphenyls (PCBs), polychlorinated dibenzo-p-dioxins, and polychlorinated dibenzofurans averaged 700 +/- 130 microg/kg, 32 +/- 23 ng/kg, and 17 +/- 5 ng/kg (lipid wt), respectively. These contaminants originate from transplacental transfer and from maternal milk, which, in turn, reflect contaminants acquired by the mother from prey during long-distance foraging trips in the northeastern Pacific Ocean. The PCB profile in the blubber of NES pups mainly was composed of penta-, hexa-, and hepta-chlorobiphenyls, possibly reflecting the deep-sea nature of the mother's diet. Our results suggest that NES pups, in contrast to pups of other pinnipeds in the eastern Pacific Ocean, are exposed to low levels of persistent organic pollutants, reflecting an open ocean signal.

Adipose Tissue↗

Reproductive success and contaminants in tree swallows (Tachycineta bicolor) breeding at a wastewater treatment plant.

The uptake and effects of contaminants were measured in the insectivorous tree swallow (Tachycineta bicolor) at a wastewater treatment site. The study examined reproductive, immunological, and growth endpoints in tree swallows exposed to chlorinated hydrocarbon contaminants and to 4-nonylphenol in wastewater lagoons at the Iona Wastewater Treatment Plant, Vancouver (BC, Canada). Clutch size was significantly lower in tree swallows breeding at Iona Island in 2000 and 2001 compared to the reference site. In 2000, fledging success was significantly lower and mean mass of nestling livers was significantly higher in the tree swallows breeding at the Iona Island Wastewater Treatment Plant. Additional factors that may influence reproductive success, such as parental provisioning and diet composition, did not differ significantly between sites. Levels of 4-nonylphenol detected in sediment and insects were elevated at the Iona Island Wastewater Treatment Plant (2000: lagoon sediment 82,000 ng/g dry wt, insects 310 ng/g wet wt; 2001: lagoon sediment 383,900 ng/g dry wt, insects 156 ng/g wet wt) compared to the reference site (2000: pond sediment 1,100 ng/g dry wt, insects not sampled; 2001: pond sediment 642 ng/g dry wt, insects 98 ng/g wet wt). These results indicate that tree swallows might be a useful indicator species for exposure to 4-nonylphenol at wastewater treatment sites: however, further work is necessary to determine the extent of uptake and effects of 4-nonylphenol in riparian insectivorous birds.

Animals↗

Low hepatic ethoxyresorufin-O-deethylase activity correlates with high organochlorine concentrations in Atlantic tomcod from the Canadian east coast.

A suppression of hepatic ethoxyresorufin-O-deethylase (EROD) activity was reported recently in large-sized Atlantic tomcod (Microgadus tomcod) from the St. Lawrence Estuary (SLE; QC, Canada), possibly related to chronic exposure to persistent contaminants and/or to emaciation. In the present study, hepatic concentrations of organochlorine contaminants and biological responses were measured in female tomcods from three estuaries located on the Canadian east coast: The SLE, the Miramichi (ME), and the Richibucto (RE) Rivers Estuaries (NB, Canada). Tomcods from the SLE had higher hepatic concentrations of organochlorine contaminants than tomcods from the ME and RE. For example, concentrations of polychlorinated biphenyls (PCBs, lipid wt) were 2.5 to 4 times higher, and concentrations of mirex and chlordanes were 6 times higher, in tomcods from the SLE than in tomcods from the other sites. Concentrations of polycyclic aromatic hydrocarbons (PAHs) metabolites in the bile did not differ among sites. The pattern of biological responses differed markedly between the SLE and the two other sites. Tomcods from the SLE had 1.5 times higher concentrations of DNA adducts and 2 times higher rates of hepatocellular proliferation, but 20 times lower hepatic EROD activity, than tomcods from the ME and RE. Lipid content was not correlated with EROD activity, indicating that low hepatic lipid content alone does not cause suppression of EROD activity in Atlantic tomcod. In contrast, for the three sites combined, EROD activity decreased as concentrations of PCBs increased. Within sites, hepatic PCB concentrations increased as lipid content decreased. This study supports the hypothesis that low EROD activity in SLE tomcods is related to chronic exposure to organochlorine contaminants.

Animals↗

Magnification and toxicity of PCBs, PCDDs, and PCDFs in upriver-migrating Pacific salmon.

The depletion of lipids associated with pre-spawning migration of Pacific salmon has the potential to magnify concentrations of hydrophobic organic contaminants (HOCs), which elevates risk of toxic effects. We present data from a field study of sockeye salmon (Oncorhynchus nerka) migrating to spawn in Great Central Lake, BC, which demonstrate that pre-spawning migration causes a magnification of PCB, PCDD, and PCDF concentrations in female gonads (1.9-2.5-fold), female soma (3.4-5.6-fold), and male soma (5.6-9.7-fold). We further develop a model of prespawning migration chemical magnification for sockeye salmon stocks as a function of migration distance. This model is shown to be consistent with available empirical data on pre-spawning magnification and predicts magnification factors ranging between 1.4 and 7.9 in gonad and between 1.6 and 10.4 in soma in seven Pacific salmon stocks in British Columbia. Post-migration (prespawning) toxic equivalent dioxin concentrations in roe were measured to be approximately 3 pg/g lipid in salmon from the Great Central Lake sockeye stock and estimated to range between 1.5 pg/g lipid for the shortest-migrating stocks and 7 pg/g lipid for the longest-migrating stocks. Concentrations in certain stocks approach or exceed the concentration of 3 pg/g lipid associated with 30% egg mortality in Oncorhynchus mykiss. This indicates the potential for population-level effects of current contaminant levels. It also suggests that historic contaminant concentrations, which were greater than current concentrations, may have contributed significantly to the decline of certain Pacific salmon stocks in British Columbia.

Animal Migration↗

PBDEs, PBBs, and PCNs in three communities of free-ranging killer whales (Orcinus orca) from the northeastern Pacific Ocean.

Polybrominated diphenyl ethers (PBDEs), polybrominated biphenyls (PBBs), and polychlorinated naphthalenes (PCNs) were quantified in blubber biopsy samples collected from free-ranging male and female killer whales (Orcinus orca) belonging to three distinct communities (southern residents, northern residents, and transients) from the northeastern Pacific Ocean. High concentrations of sigmaPBDE were observed in male southern residents (942+/-582 ng/g Iw), male and female transients (1015+/-605 and 885+/-706 ng/g Iw, respectively), and male and female northern residents (203+/-116 and 415+/-676 ng/g Iw, respectively). Because of large variation within sample groups, sigmaPBDE levels generally did not differ statistically with the exception of male northern residents, which had lower sigmaPBDE concentrations than male southern residents, male transients, and female transients, perhaps reflecting the consumption of less contaminated prey items. Male transient killer whales, which consume high trophic level prey including other cetaceans and occasionally spend time near populated areas, had sigmaPBDE concentrations approximately equal to southern residents. No significant age-related relationships were observed for sigmaPBDE concentrations. sigmaPBDE concentrations were approximately 1-3 orders of magnitude greater than those of sigmaPBB (3.0-31 ng/g Iw) and sigmaPCN (20-167 ng/g Iw) measured in a subset of samples, suggesting that PBDEs may represent a contaminant class of concern in these marine mammals.

Adipose Tissue↗

Semivolatile organic compounds in window films from lower Manhattan after the September 11th World Trade Center attacks.

The September 11th World Trade Center (WTC) terrorist attacks resulted in the large-scale release of contaminants that were deposited on the environment of New York City (NYC). Six weeks after the attacks, samples of an organic film on window surfaces were collected and analyzed for polybrominated diphenyl ethers (PBDE), polychlorinated biphenyls (PCB), polychlorinated naphthalenes (PCN), polycyclic aromatic hydrocarbons (PAH), and organochlorine pesticides (OCPs). Concentrations dropped by an order of magnitude within 1 km of the WTC and reached background concentrations by 3.5 km. Concentrations within 1 km of the WTC averaged 3280 ng/m2 for sigmaPBDE, 900 ng/m2 for sigmaPCB, 33 ng/m2 for sigmaPCN, and 77100 ng/m2 for sigmaPAH. Congener profiles of the sites nearest the WTC suggested a combination of combustion and evaporative sources of all compounds, whereas the background sites exhibited profiles consistent with evaporative sources. PBDE profiles showed enrichment in lower molecular weight congeners near the WTC, suggesting that these congeners were formed as a result of the combustion conditions. Homologue fractions of PCN combustion markers were approximately 2-9 times greater at near WTC sites compared to background NYC. Gas-phase air concentrations were back-calculated from measured film concentrations using the film-air partition coefficient (KFA), and calculated air concentrations followed spatial trends observed in films.

Air Pollutants↗

Distribution of phthalate esters in a marine aquatic food web: comparison to polychlorinated biphenyls.

Dialkyl phthalate esters (DPEs) are widely used chemicals, with over 4 million tonnes being produced worldwide each year. On the basis of their octanol-water partition coefficients (Kow), which range from 10(1.61) for dimethyl phthalate to 10(9.46) for di-iso-decyl phthalate, certain phthalate esters have the potential to bioconcentrate and biomagnify in aquatic food webs. However, there are no reported field studies on the trophodynamics of phthalate ester in aquatic food webs. This study reports the distribution of 8 individual phthalate esters (i.e., dimethyl, diethyl, di-isobutyl, di-n-butyl, butylbenzyl, di(2-ethylhexyl), di-n-octyl, and di-n-nonyl) and 5 commercial isomeric mixtures (i.e., di-iso-hexyl (C6), di-iso-heptyl (C7), di-iso-octyl (C8), di-iso-nonyl (C9), and di-iso-decyl (C10)) in a marine aquatic food web. DPE concentrations were determined in 18 marine species, representing approximately 4 trophic levels. Co-analysis of DPEs and 6 PCB congeners (i.e., PCB-18, 99, 118, 180, 194, and 209) in all samples produced a direct comparison of the bioaccumulation behavior of PCBs and DPEs. Lipid equivalent concentrations of the PCBs increased with increasing trophic position and stable isotope ratios (delta15N). The Food-Web Magnification Factor (FWMF) of the PCB congeners ranged from 1.8 to 9.5. Lipid equivalent concentrations of low and intermediate molecular weight DPEs (i.e., C1-C7 DPEs: dimethyl, diethyl, di-iso-butyl, di-n-butyl, benzylbutyl, and C6 and C7 isomers) did not exhibit statistically significant trends with trophic position or stable nitrogen isotope ratios (delta15N) in the food web and FWMFs were not significantly different from 1. Lipid equivalent concentrations of the high-molecular-weight DPEs (i.e., C8-C10 DPEs: di(2-ethylhexyl), di-n-octyl, di-n-nonyl, C8, C9, and C10) declined significantly with increasing trophic position and stable isotope ratios (delta15N), producing FWMFs between 0.25 and 0.48. These results show that all DPEs tested did not biomagnify in the studied aquatic food web whereas PCBs did biomagnify.

Animals↗

Spatial variation in hepatic levels and patterns of PCBs and PCDD/Fs among young-of-the-year and adult Atlantic tomcod (Microgadus tomcod) in the Hudson River estuary.

Full congener-specific polychorinated biphenyl (PCB) and partial-congener-specific polychorinated dibenzo-p-dioxin/furan (PCDD/F) analyses were performed on livers from young-of-the-year (YOY) and adult Atlantic tomcod from the Hudson River estuary including multiple sites along the main-stem Hudson River and Newark Bay/Hackensack River, NJ, and from a reference river, the Miramichi River, NB. Highest hepatic burdens of PCBs were found in fish collected in the main-stem Hudson River between river miles (RM) 37 and 50 and in Newark Bay/Hackensack River. By far, the highest concentrations of PCDD/Fs were seen in fish from Newark Bay/Hackensack River. The di- to tetrachlorinated biphenyls dominated the PCB composition in YOY tomcod, whereas the penta- to nonachlorinated biphenyls predominated in adults with particular prevalence of the 2,4,5-substituted diortho congeners. Overall, using a direct mixing model an aroclor composition of approximate 1:1:1, A1242:A1254:A1260, was calculated from the hepatic PCB profiles in YOY tomcod. A linear increase in A1242 characteristics with river mile was seen in YOY collected between RM 0 and RM 80, which was likely due to the well-characterized A1242 source from the former capacitor manufacturing plants located upriver. However, tomcod caught upstream of RM 80 exhibited a PCB pattern with decreasing A1242 characteristics, and it was hypothesized that this was due to the increased depuration or decreased uptake of low chlorinated (log K(OW) < 6) congeners upon entry of the fish into freshwater from brackish water. The most abundant tetra-octa PCDD/F chlorohomologue in tomcod collected from the main stem of the Hudson River was TCDF, whereas 2,3,7,8-TCDD was the major congener detected in tomcod from Newark Bay/Hackensack River, which showed elevated total PCDD/F levels compared to tomcod from the main-stem Hudson River.

Animals↗

Spatial distribution of polybrominated diphenyl ethers in southern Ontario as measured in indoor and outdoor window organic films.

Organic films were collected from indoor and outdoor window surfaces, along an urban-rural transect extending northward from Toronto, Ontario, Canada, and analyzed for 41 polybrominated diphenyl ether congeners (PBDE). For exterior films, urban sigmaPBDE concentrations were approximately 10x greater than rural concentrations, indicating an urban-rural gradient and greater PBDE sources in urban areas. Urban films ranged from 2.5 to 14.5 ng/m2 (mean = 9.0 ng/ m2), excluding the regional "hotspot" Electronics Recycling Facility, compared to 1.1 and 0.56 ng/m2 at the Suburban and Rural sites. Interior urban films (mean = 34.4 ng/m2) were 3 times greater than rural films (10.3 ng/m2) and were representative of variations in building characteristics. Indoor films were 1.5-20 times greater than outdoor films, consistent with indoor sources of PBDEs and enhanced degradation in outdoor films. Congener profiles were dominated by BDE-209 (51.1%), consistent with deca-BDE as the main source mixture, followed by congeners from the penta-BDE mixture (BDE-99:13.6% and -47:9.4%) and some octa-BDE (BDE-183:1.5%). Congener patterns suggest a degradative loss of lower brominated compounds in outdoor films versus indoor films. Gas-phase air concentrations were back-calculated from film concentrations using the film-air partition coefficient (K(FA)). Mean calculated air concentrations were 4.8 pg/m3 for outdoor and 42.1 pg/m3 for indoor urban sites, indicating that urban indoor air is a source of PBDEs to urban outdoor air and the outdoor regional environment.

Air Pollutants↗

Harbor seals (Phoca vitulina) in British Columbia, Canada, and Washington State, USA, reveal a combination of local and global polychlorinated biphenyl, dioxin, and furan signals.

The harbor seal (Phoca vitulina) can serve as a useful indicator of food web contamination by persistent organic pollutants (POPs) because of its high trophic level, wide distribution in temperate coastal waters of the Northern Hemisphere, and relative ease of capture. In 1996 through 1997, we live-captured 60 harbor seal pups from three regions, spanning remote (Queen Charlotte Strait, BC, Canada), moderately industrialized (Strait of Georgia, BC, Canada), and heavily industrialized (Puget Sound, WA, USA) marine basins straddling the Canada-United States border. Biopsy samples of blubber were taken and analyzed for congener-specific polychlorinated biphenyls (PCBs), polychlorinated dibenzo-p-dioxins (PCDDs), and polychlorinated dibenzofurans (PCDFs) by using high-resolution gas chromatography-high-resolution mass spectrometry. Harbor seals in Puget Sound were heavily contaminated with PCBs, whereas seals from the Strait of Georgia had relatively high concentrations of PCDDs and PCDFs. Pattern evaluation and principal components analysis suggested that proximity to sources influenced the mixture to which seals were exposed, with those inhabiting more remote areas being exposed to lighter PCB congeners (those with lower Henry's law constant and K(ow)) that disperse more readily through atmospheric and other processes. Total toxic equivalents to 2,3,7,8-tetrachlorodibenzo-p-dioxin for the PCBs, PCDDs, and PCDFs suggest that Puget Sound seals are at greatest risk for adverse health effects, and that PCBs represent the class of dioxinlike contaminants of greatest concern at all sites.

Adipose Tissue↗

Congener-based Aroclor quantification and speciation techniques: a comparison of the strengths, weaknesses, and proper use of two alternative approaches.

This paper compares two previously published methods, an Aroclor estimation method and a mixing model method, that relate Aroclor contamination to congener specific data in environmental samples. The Aroclor estimation method, which is consistent with U.S. EPA Method 8082, uses a limited set of congener specific data to estimate Aroclor contributions to the sample, while the mixing model method uses the full congener data to model sample compositions as linear combinations of Aroclors. The performance of these methods are compared, using 181 samples at a variety of trophic levels, in terms of (a) total PCB concentrations, (b) compositional modification levels from original Aroclors, and (c) determination of the Aroclor mixture or mixtures best describing the sample (Aroclor speciation). We find that the two methods agree in all three terms for samples of low trophic level, but disagree for samples of higher tropic levels. Most significantly, the comparison reveals systematic overestimation of total PCB content by the Aroclor estimation method for samples at high trophic levels. The implication is that Aroclor determinations using persistent congeners cannot reliably be used as surrogates for total PCB concentration. The strengths and weaknesses of each method are detailed.

Animals↗