Biomedical subjects

Eddy Y Zeng

Publications and source records attributed to Eddy Y Zeng.

At least 19 recordsLinked to original sources

PubMed2006

Predicting organic contaminant concentrations in sediment porewater using solid-phase microextraction.

Because of its cost and time saving features, solid-phase microextraction (SPME) is a leading candidate as a biomimic technique in assessing the bioavailable fraction of hydrophobic organic contaminants (HOCs) in sediment porewater. However, no predictive modeling framework in which to systematically address the effect of key parameters on SPME performance for this application exists. In this study, we derived two governing equations to predict (1) the minimum sediment volume (V(s)min) required to achieve non-depletive conditions, and (2) dissolved phase HOC porewater concentrations (C(pw)) as functions of HOC- and sediment specific characteristics in a conceptual three compartment system. The resulting model predicted that V(s)min was independent of HOC concentrations both in sediment and porewater, but did vary with hydrophobicity (characterized by logK(ow)), the fraction of sediment porewater (f(pw)), and the volume (V(f)) of the SPME sorbent phase. Moreover, the effects of these parameters were minimized (i.e., V(s)min reached plateaus) as logK(ow) approached 4-5. Model predictions of C(pw), a surrogate for SPME-based detection limits in porewater, decreased with increasing sediment volume (V(s)) at low V(s) values, but rapidly leveled off as V(s) increased. A third result suggested that the sediment HOC concentration required for SPME is completely independent of K(ow). These results suggest that relatively small sediment volumes participate in exchange equilibria among sediment, porewater and the SPME fiber, and that large sediment HOC reservoirs are not needed to improve the detection sensitivity of SPME-based porewater samplers. The ultimate utility of this modeling framework will be to assist future experimental designs and help predict in situ bioavailability of sediment-associated HOCs.

Algorithms↗

PubMed2006

A numerical scheme to diagnose interferences in gas chromatography-mass spectrometry quantitation of coeluting isotopically labeled and unlabeled counterparts with partially overlapping ion profiles.

Quantitation of chromatographically coeluting compounds with partially overlapping mass profiles is a challenging task, especially if only a low-resolution mass spectrometer is available. To examine whether theoretical predictions can be utilized to determine the appropriate concentration ranges of the coeluting compounds that satisfy the non-interfering condition, we utilized an algorithm based upon a two-component model to compare the experimentally measured and predicted quantitation errors. Selected unlabeled and 13C-labeled polychlorinated biphenyl (PCB) congeners were investigated as model compounds. Standard solutions containing various concentration ratios of the unlabeled and 13C-labeled PCB congeners were analyzed, and the data were used to compare with theoretical predictions derived from the chlorine isotopic distributions (35Cl and 37Cl). Good agreements between experimental predictions and theoretical predictions were found on the magnitude of interferences for quantitation of 13C-labeled PCB congeners, as well as on the variability of the quantitation errors with the concentration ratio of 13C-labeled and unlabeled PCB counterparts. In addition, the magnitude of interferences considered in the present study was highly dependent upon the number of coexisting ions included for quantitation and their relative abundances in the mass spectrum. All these results suggest that the magnitude of interferences in quantifying a pair of coeluting compounds with partially overlapping mass spectral profiles can be effectively determined and minimized by carefully selecting the concentration ratio of the coeluting compounds and/or the number of quantitation ions. Finally, the selection of the experimental parameters to satisfy the non-interfering condition can be made purely on the basis of theoretical considerations.

Chromatography, Thin Layer↗

PubMed2006

Polybrominated diphenyl ethers in surface sediments of the Yangtze River Delta: Levels, distribution and potential hydrodynamic influence.

A total of 32 surface sediments collected from the Yangtze River Estuary, Hangzhou Bay and the Qiantang River were analyzed for polybrominated diphenyl ethers (PBDEs). The concentrations of summation operatorPBDEs (sum of 12 PBDE congeners without BDE 209) and BDE 209 varied from n.d. to 0.55 and from 0.16 to 94.6 ng/g, respectively. The spatial variability of summation operatorPBDEs concentrations indicated that waste discharge from the urban areas might been the main source of PBDEs in the Yangtze River Delta. BDE 209 was the predominant congener (approximately 90-100%) detected among the 13 congeners, consistent with the fact that technical deca-BDE mixtures are presently the dominant technical PBDE mixtures used in China. Compared to published data acquired from other locales, PBDE congeners with less than four bromines were more abundant in the present study area. The hydrodynamic conditions may likely be a significant factor in dictating the observed levels and congener distribution patterns of PBDEs.

China↗

PubMed2006

Application of a static solid-phase microextraction procedure combined with liquid-liquid extraction to determine poly(dimethyl)siloxane-water partition coefficients for selected polychlorinated biphenyls.

A static solid-phase microextraction (SPME) procedure combined with liquid-liquid extraction (LLE) was used to determine the poly(dimethyl)siloxane (PDMS)-water partition coefficients (K(f)) for selected polychlorinated biphenyl congeners (PCBs), including PCB 1, 15, 28, 47, 101, 153, 180, 202, 206, and 209. The accuracy for the measurements of analyte concentrations in the aqueous phase was ensured with a one-to-one recovery correction strategy employing one 13C-labeled PCB congener as a surrogate standard for each unlabeled PCB counterpart. The effects of coating thickness (7, 30, and 100 microm) and sample volume (130 mL and 2 L) on the K(f) values were examined experimentally and confirmed with paired t-tests. Significant dependence of K(f) values on coating thickness was found for a few heavily chlorinated congeners only, and was tentatively attributed to the use of the inaccurate effective coating volumes and the structural variation with these PDMS coatings. In addition, no significant differences in the log K(f) values of all analytes except for PCB 206 were found between the sample sizes of 130 mL and 2 L for both the 7- and 100-microm coatings. Overall, K(f) values obtained with 2-L sample containers were consistently higher than those reported in the literature, which is attributable to the selection of appropriate equilibrium times for SPME and direct measurements of aqueous analyte concentrations with LLE in the present study.

Dimethylpolysiloxanes↗

PubMed2006

Concentration levels, compositional profiles, and gas-particle partitioning of polybrominated diphenyl ethers in the atmosphere of an urban city in South China.

Air samples were collected in June of 2004 from four sites in the city of Guangzhou, a typical urban center in South China, to determine the levels, compositional profiles, and gas-particle distribution of 11 polybrominated diphenyl ether (PBDE) congeners (BDE-28, -47, -66, -100, -99, -85, -154, -153, -138, -183, and -209). The arithmetic mean atmospheric concentrations of sigmaPBDEs (sum of all target PBDE congeners except for BDE-209) in samples from the urban and city background sites were comparable to or slightly higher than those from other places around the world. The arithmetic mean atmospheric concentrations of BDE-209, however, were higherthan those in North America and Europe, and similar to the values from Japan. Congener compositions were dominated by BDE-209 in all (>70%) but an industrial site, with an average abundance of 48% for BDE-209. The PBDE patterns were generally similar to that in the technical penta-BDE mixture, Bromkal 70-5DE. Partitioning of PBDEs between the gas and particle phases (Kp) was well correlated with the subcooled liquid vapor pressure (PLO) for all of the samples, but the relationship differed between samples from different sites. The measured fractions of PBDEs in the particulate phase were compared to the predictions from the Junge-Pankow adsorption and KOA-based absorption models. The results indicated that the KOA-based model worked better than the Junge-Pankow model that tended to overestimate the particulate fractions for most PBDE congeners.

Adsorption↗

PubMed2006

Distribution and mass inventories of polycyclic aromatic hydrocarbons and organochlorine pesticides in sediments of the Pearl River Estuary and the northern South China Sea.

Surface sediment (0-5 cm) samples were collected from the Pearl River Estuary (PRE) and the adjacent northern South China Sea (SCS) in July 2002 and analyzed for 25 polycyclic aromatic hydrocarbons (PAHs) and 8 organochlorine pesticides (OCPs) including dichlorodiphenyltrichloroethanes (DDTs), hexachlorocyclohexanes (HCHs), and heptachlor. The total PAHs and OCPs concentrations were 138-1100 and 0.18-3.57 ng/g dry weight, respectively. Compositional pattern analysis suggested that PAHs in the PRE were derived from both pyrogenic and petrogenic sources, whereas most PAHs in the northern SCS were pyrogenically originated. The concentrations of both PAHs and OCPs were higher in the PRE than in the northern SCS, and a decreasing trend with the distance from the estuary to the open sea was observed. In addition, perylene was a predominant component in all samples and clustered with PAH compounds with high log Kow values (from phenanthrene). These findings indicated that river outflows were the major source of contamination in the offshore sediments. A preliminary assessment suggested that atmospheric deposition contributed only a minor portion of PAHs or OCPs in the sediments of the northern SCS. The sediment (0-5 cm) mass inventories were 126 and 423 metric tons for PAHs and were 0.4 and 1.4 metric tons for OCPs in the PRE and the northern SCS, respectively. Clearly, contaminated sediments of the northern SCS may be a potential source of PAHs and OCPs to the global oceans.

Air Pollutants↗

PubMed2005

Distribution and mass inventory of total dichlorodiphenyldichloroethylene in the water column of the southern California bight.

A large-scale survey on the area and depth stratified distribution of dichlorodiphenyltrichloroethane (DDT; mainly p,p'- and o,p'-dichlorodiphenyldichloroethylene (DDE)) contamination in the water column of the Southern California Bight (SCB) was conducted in 2003-2004 using a solid-phase microextraction-based sampling technique. Dissolved-phase DDEs were clearly widespread, with the central SCB containing the highest levels, and the Palos Verdes Shelf sediments have remained the dominant source of DDT compounds to the SCB. The p,p'- and o,p'-DDE concentrations ranged from < 0.073 to 2.6 ng/L and from < 0.043 to 0.26 ng/L, respectively, clearly elevated with respect to measured values from across the globe. DDEs were hypothesized to have been transported from the historically contaminated zone on the Palos Verdes Shelf to other areas via a repeated process of sediment resuspension/deposition and short-range advection. Total mass inventories were estimated at 14 and 0.86 kg for p,p'- and o,p'-DDE, respectively, for the sampled area, resulting in p,p'- and o,p'-DDE mass inventories for the entire SCB of 230 and 14 kg, respectively. Furthermore, total fluxes of p,p'-DDE were estimated to be in the range of 0.8 to 2.3 metric tons per year. These results suggest that the SCB has been and continues to be a significant source of DDT contamination to the global oceans.

California↗

PubMed2005

Polybrominated diphenyl ethers in airborne particulates collected during a research expedition from the Bohai Sea to the Arctic.

In July to September 2003, particulates in the oceanic atmosphere from the Bohai Sea to the high Arctic (37 degrees N to 80 degrees N) were collected aboard a research expedition icebreaker, Xuelong (Snow Dragon), under the 2003 Chinese Arctic Research Expedition Program (CHINARE 2003). These samples were analyzed to elucidate the atmospheric distributions of polybrominated diphenyl ethers (PBDEs) in the North Pacific Ocean and adjacent Arctic region. The levels of 11 PBDE congeners (BDE-28, -47, -66, -100, -99, -85, -154, -153, -138, -183, and -209; the sum was defined as sigma11PBDE) in the oceanic atmosphere of Far East Asia (34-48 degrees N/122-148 degrees E) ranged from 2.25 to 198.9 pg/m3 with a mean of 58.3 pg/m3. BDE-47, -99, -100, and -209 were the dominant congeners in all the samples, suggesting that the widely used commercial penta- and deca-BDE products were the original sources. The PBDE levels exhibited a decreasing trend from the mid- to high-latitudinal regions of the North Pacific Ocean, probably resulting from dilution, deposition, and decomposition of PBDEs during long-range transport of air masses. On the other hand, no apparent geographical pattern of PBDE distribution was observed within the Arctic, attributable to unstable air circulation and strong air mixing. Correlations among the PBDE congeners suggested that air masses collected from the North Pacific Ocean were relatively fresh, whereas those from the Arctic were aged as a result of photodecompoisiton. The higher average level (17.3 pg/m3) of PBDE congeners in the Arctic than those in the adjacent North Pacific Ocean (12.8 pg/m3) or other remote areas reported in the literature was attributed to the impact of the North American continent and temperature effects, which was consistent with the hypotheses of global fractionation.

Air Movements↗

PubMed2005

Distribution of polybrominated diphenyl ethers in sediments of the Pearl River Delta and adjacent South China Sea.

Spatial and temporal distributions of polybrominated diphenyl ethers (PBDEs) in sediments of the Pearl River Delta (PRD) and adjacent South China Sea (SCS) of southern China were examined. A total of 66 surface sediment samples were collected and analyzed to determine the concentrations of 10 PBDE congeners (BDE-28, -47, -66, -100, -99, -154, -153, -138, -183, and -209). The concentrations of BDE-209 and SigmaPBDEs (defined as the sum of all targeted PBDE congeners except for BDE-209) ranged from 0.4 to 7340 and from 0.04 to 94.7 ng/g, respectively. The SigmaPBDEs concentrations were mostly < 50 ng/g, within the range for riverine and coastal sediments around the world, whereas the BDE-209 concentrations at the most contaminated sites were at the high end of the worldwide figures. Congener compositions were dominated by BDE-209 (72.6 - 99.7%), with minor contributions from penta- and octa-BDEs. Slightly different PBDE compositions were observed among samples collected from different locations, attributable to possible decomposition of highly brominated congeners and/or redistribution between particles of various sizes during atmospheric or fluvial transportation. The PBDE patterns in the SCS and Pearl River Estuary sediments were similar to those in sediments of the Zhujiang and Dongjiang Rivers, reflecting the widespread influence from local inputs. Analyses of two short sediment cores collected from the Pearl River Estuary showed that concentrations of BDE-209 rapidly increased in the upper layers of both cores, coincident with the growth of the electronics manufacturing capacities in the PRD region. The major sources of PBDEs were probably waste discharges from the cities of Guangzhou, Dongguan, and Shenzhen, the three fastest growing urban centers in the PRD.

China↗

PubMed2005

Determination of polydimethylsiloxane-seawater distribution coefficients for polychlorinated biphenyls and chlorinated pesticides by solid-phase microextraction and gas chromatography-mass spectrometry.

Applications of solid-phase microextraction (SPME) in the measurement of very hydrophobic organic compounds (VHOCs) are limited, partly due to the difficulty of calibrating SPME fibers for VHOCs. This study used a static SPME strategy with a large sample volume (1.6 L) and a five-point calibration procedure to determine the distribution coefficients for a large suite of polychlorinated biphenyls (PCBs) and chlorinated pesticides between a polydimethylsiloxane (PDMS) phase (100 microm thickness) coated on a glass fiber and seawater. An extraction time of 12 days was deemed adequate for equilibrium calibration from kinetic experiments. Two groups of randomly selected fibers divided into three batches (up to nine fibers in each batch) were processed separately with two gas chromatography-mass spectrometry (GC-MS) systems. Matrix effects arising from losses of the analytes to glass container walls and stirring bars were corrected. Relative standard deviations within the same batch were generally smaller than those for the entire group. Furthermore, KfVf (Kf and Vf are the distribution coefficient of an analyte between the polymer-coated fiber and aqueous phase and the fiber volume, respectively) values determined with two GC-MS systems were statistically different. These results indicate the calibrated KfVf values were less affected by the random selection of SPME fibers than by other experimental conditions, and therefore average KfVf values may be used for the same type of commercially available SPME fibers. The relative accuracy of our calibration method was similar to that of a previous study [P. Mayer. W.H.J. Vaes, J.L.M. Hermens, Anal. Chem. 72 (2000) 459] employing different coating thickness and calibration procedure. The present study also obtained a bell-shaped relationship between log Kf and log Kow (octanol-water partition coefficient) for PCB congeners with the maximum log Kf corresponding to log Kow approximately 6.5. This bell-shaped relationship was attributed mainly to steric effects arising from the interplay between the PDMS thickness and molecular sizes of the target analytes.

Chemistry Techniques, Analytical↗

PubMed2005

Abundances, depositional fluxes, and homologue patterns of polychlorinated biphenyls in dated sediment cores from the Pearl River Delta, China.

Despite the recent efforts to investigate the distribution and fate of persistent organic pollutants in the tropical and subtropical regions of Asia, very little was known about the temporal change of polychlorinated biphenyls (PCBs) in the environmental ecosystem of China. In this study, three dated sediment cores collected from the Pearl River Delta of southern China were analyzed for a large suite of PCB congeners, from which the temporal profiles of PCB abundances, fluxes, and homologue patterns were constructed. The sedimentary inventories of total PCBs at the sampling sites ranged from 480 to 1310 ng/cm2, at the low end of the worldwide figures. Although production and use of PCBs have been banned or highly restricted in China since the early 1980s, the fluxes of total PCBs continued to increase in the Pearl River Delta sediments. There was a concurrent increase of PCB fluxes and gross domestic product per capita in the region from 1980 to 1997, and a decline of agricultural land use was evident at the same time. Apparently, large-scale land transform since the early 1980s as well as emissions from the PCB-containing electrical equipments were responsible for the sharp rise of PCB fluxes in the recent sediments. The difference in the PCB homologue patterns from 1940 to the mid-1970s was probably indicative of the different timelines of PCB usage in Macao/Hong Kong and mainland China and the differenttypes of technical PCBs commercially used. PCBs were detectable in sediments deposited well before the time frame when production of PCBs began (before 1930) and were relatively enriched in the less chlorinated homologue groups (3Cl and 4Cl PCBs), suggesting the downward mobility of lightly chlorinated PCB congeners in the sediment column.

China↗

PubMed2005

Assessing the genotoxicity of imidacloprid and RH-5849 in human peripheral blood lymphocytes in vitro with comet assay and cytogenetic tests.

A combined approach employing comet assay and micronucleus (MN) and sister chromatid exchanges (SCE) tests was utilized to assess the genotoxicity of two pesticides, imidacloprid [1-(6-chloro-3-pyridylmethyl)-N-nitro-imidazolidin-2-ylideneamine] and RH-5849 [2'-benzoyl-1'-tert-butylbenzoylhydrazine], on human peripheral blood lymphocytes in vitro. No significant difference in the frequencies of MN and SCE from the negative groups (P>0.05) was observed at low dose levels (i.e., 0.05 mg/L for imidacloprid and 5mg/L for RH-5849). As the concentrations of imidacloprid and RH-5849 were increased to 0.1 and 25 mg/L, respectively, significant effects to the frequencies of MN and SCE (P<0.05) were achieved relative to those of the negative controls. MN and SCE frequencies increased similarly in a dose-related manner with both pesticides. With the comet assay, however, the distribution of DNA damage grades in all the pesticide-treated groups was significantly different from those in the control (P<0.01). DNA damage scores increased with the exposure levels of both pesticides, and linear dose-effect relationships were observed for both imidacloprid (r2=0.98) and RH-5849 (r2=0.92). The cytogenetic techniques and comet assay revealed potential adverse effects of both imidacloprid and RH-5849 in human peripheral blood lymphocytes in vitro. Combination of the comet assay and cytogenetic tests appears commendable to assess the potential risks of human exposure to the pesticides.

Adult↗

PubMed2004

Use of fecal steroids to infer the sources of fecal indicator bacteria in the Lower Santa Ana River Watershed, California: sewage is unlikely a significant source.

The Santa Ana River (SAR), CA and adjacent wetlands have been identified as potential sources of fecal indicator bacteria (FIB) to the surf zone at Huntington Beach, CA. A suite of fecal steroids, including coprostanol (COP), epicoprostanol (eCOP), cholesterol (CHOE), cholestanol (CHOA), alpha-cholestanone (aONE), beta-cholestanone (bONE), beta-sitosterol (bSIT), stigmasterol (STIG), stigmastanol (STAN), and campesterol (CAM), were used as chemical markers to examine whether sewage was a significant source of FIB within the lower Santa Ana River watershed. A total of 54 water samples were collected from three locations in the intertidal zone near the mouth of the Santa Ana River at different tidal stages. Steroid ratios in SAR samples were different from those found in raw and treated sewage from a local wastewater treatment plant or in nearby effluent plume and did not appear to be influenced by the sampling location, daily tides, and spring/neap tidal cycle. The characteristics of steroid ratios suggested a diagenetic ratherthan a biogenic source forthe COP content of the samples. The log-based concentrations of COP and FIB in the SAR samples were not significantly correlated, inconsistent with sewage being the source of FIB in the study area. In addition, multivariate statistical analysis showed that the concentrations of FIB were better correlated with bird fecal steroids than with the typical sewage sterols. The results implied that sewage was not a significant source of fecal steroids, and therefore perhaps FIB to the study area. Instead, birds may be one possible source of the intermittently high levels of FIB observed in the lower Santa Ana River watershed and the nearby surf zone.

Animals↗

PubMed2004

Development of a solid-phase microextraction-based method for sampling of persistent chlorinated hydrocarbons in an urbanized coastal environment.

Solid-phase microextraction (SPME) has been used as an in situ sampling technique for a wide range of volatile organic chemicals, but SPME field sampling of nonvolatile organic pollutants has not been reported. This paper describes the development of an SPME-based sampling method employing a poly(dimethylsiloxane) (PDMS)-coated (100-microm thickness) fiber as the sorbent phase. The laboratory-calibrated PDMS-coated fibers were used to construct SPME samplers, and field tests were conducted at three coastal locations off southern California to determine the equilibrium sampling time and compare the efficacy of the SPME samplers with that of an Infiltrex 100 water pumping system (Axys Environmental Systems Ltd., Sidney, British Columbia, Canada). p,p'-DDE and o,p'-DDE were the components consistently detected in the SPME samples among 42 polychlorinated biphenyl congeners and 17 chlorinated pesticidestargeted. SPME samplers deployed attwo locations with moderate and high levels of contamination for 18 and 30 d, respectively, attained statistically identical concentrations of p,p'-DDE and o,p'-DDE. In addition, SPME samplers deployed for 23 and 43 d, respectively, at a location of low contamination also contained statistically identical concentrations of p,p'-DDE. These results indicate that equilibrium could be reached within 18 to 23 d. The concentrations of p,p'-DDE, o,p'-DDE, or p,p'-DDD obtained with the SPME samplers and the Infiltrex 100 system were virtually identical. In particular, two water column concentration profiles of p,p'-DDE and o,p'-DDE acquired by the SPME samplers at a highly contaminated site on the Palos Verdes Shelf overlapped with the profiles obtained by the Infiltrex 100 system in 1997. The field tests not only reveal the advantages of the SPME samplers compared to the Infiltrex 100 system and other integrative passive devices but also indicate the need to improve the sensitivity of the SPME-based sampling technique.

Chromatography, Gas↗

PubMed2004

Evaluation of potential molecular markers for urban stormwater runoff.

Source specificity and persistence of several sulfur-polycyclic aromatic hydrocarbons (S-PAHs), nitro-PAHs (N-PAHs), and triphenylene were examined via analyses of stormwater runoff and wastewater effluent samples and spiked samples upon exposure to sunlight. Samples were collected during the 1997/1998 wet weather season from two major storm channels and four major wastewater treatment plants in southern California. Among the target compounds examined, 2-(4-morpholinyl)benzothiazole, dibenzothiophene, and triphenylene/chrysene were detected in storm runoff only. However, 2-(4-morpholinyl)benzothiazole appeared to degrade rapidly in seawater and sediment after sunlight exposure, which might impede its use as a runoff indicator. Dibenzothiophene and triphenylene also degraded quickly in sunlight-exposed seawater samples, but remained fairly abundant in sediments after six months of exposure to sunlight. They are by far the most promising candidates of urban runoff markers based on the criteria of abundance, source specificity, and persistence, although more research efforts are needed to ensure that no other sources would also contribute significantly to their presence in the aquatic environment.

Benzothiazoles↗

PubMed2003

Distribution of polycyclic aromatic hydrocarbons in the coastal region off Macao, China: assessment of input sources and transport pathways using compositional analysis.

The coastal region off Macao is a known depositional zone for persistent organic pollutants (POPs) in the Pearl River Delta and Estuary of southern China and an important gateway for the regional contributions of contamination to the globe. This paper presents a comprehensive assessment of the input sources and transport pathways of polycyclic aromatic hydrocarbons (PAHs) found in the coastal sediments of Macao, based on measurements of 48 2-7 ring PAHs and 7 sulfur/oxygenated (S/O) PAH derivatives in 45 sediment, 13 street dust, and 68 aerosol samples. Total sediment PAHs concentrations ranged from 294 to 12741 ng/g, categorized as moderate contamination compared to other regions of Asia and the world. In addition, the PAH compounds appeared to be bound more strongly to aromatics-rich soot particles than to natural organic matter, implying a prevailing atmospheric transport route for PAHs to Macao's coast. Compositional analysis and principal component analysis (PCA) suggested that different classes of PAHs in the coastal sediments of Macao may have been derived from different input sources via various transport pathways. For example, alkylated and S/O PAHs were likely derived from fossil fuel leakage and transported to sediments by both aerosols particles and street runoff. High-molecular-weight parent PAHs were predominantly originated from automobile exhausts and distributed by direct and indirect atmospheric deposition. Low-molecular-weight parent PAHs, on the other hand, may have stemmed from lower temperature combustion and fossil fuel (such as diesel) spillage from ships and boats and were transported to sediments by river runoff or direct discharge as well as by air-water exchange.

Air Pollutants↗

PubMed2003

Evaluation of polychlorinated biphenyl bioaccumulation patterns in white sea urchins (Lytechinus pictus) using multiple approaches.

The bioaccumulation of polychlorinated biphenyls (PCBs) from three amended field-contaminated sediments (with total PCB concentrations of approximately 4, 10, and 100 microg/g dry wt) by white sea urchins (Lytechinus pictus) was evaluated using multiple statistical and theoretical approaches. Similarity analysis of the PCB bioaccumulation patterns, based on the concept of ecological communities, showed that the PCB patterns in the sea urchins and source sediments were essentially identical for all three sediment concentrations. However, affinity analysis did show some preference for bioaccumulation of higher-molecular-weight and more hydrophobic congeners by the urchins. The affinity analysis also showed that within a homologous series, bioaccumulation increased with increasing hydrophobicity. The biota-sediment accumulation factor (BSAF) profiles for the two lower concentration sediments (A and B) were found to be statistically different from the high concentration sample (sediment C) by a multivariate analysis of variance (MANOVA). The relationship between the measured apparent organic carbon-normalized partition coefficients (K(OC)) and octanol-water partition coefficient (K(OW)) (log based) suggested a significant departure from thermodynamic equilibrium. A nonequilibrium, steady-state bioaccumulation model was found to correctly predict the observed experimental bioaccumulation patterns. To improve the model performance, a hydrophobic term was introduced to account for the drop-off in BSAF profiles with log K(OW) > or = 6.5. This study showed that nonequilibrium, steady-state models are far superior to equilibrium partitioning-based models for understanding the bioaccumulation of organic chemicals by sea urchins.

Animals↗

PubMed2003

Toxic effects of polychlorinated biphenyl bioaccumulation in sea urchins exposed to contaminated sediments.

The uptake patterns and toxicity of polychlorinated biphenyl (PCB) congeners in the white sea urchin, Lytechinus pictus, on exposure to contaminated sediments were investigated. First-order modeling of uptake of the 10 most abundant PCB congeners or domains (containing more than one coeluting congener) by L. pictus indicated that a 35-d exposure was insufficient to reach steady state. Bioaccumulation of PCBs in sea urchins exhibited substantial difference between field and amended sediments, suggesting that caution must be exercised in sample preparation. Some evidence was observed of dependence of measured biota-sediment accumulation factors (BSAFs) on K(ow), indicating that equilibrium partitioning of PCBs may not always be achieved between biota lipid, sediment organic carbon, and water. Survival of L. pictus was unaffected by exposure to field and amended sediments with PCB concentrations varying more than three orders of magnitude. The growth measures (diameter, wt, and gonad wt) were significantly reduced in L. pictus exposed to San Diego Bay ([SDB]; San Diego, CA, USA) sediment, whereas they were relatively unaffected after exposure to amended sediments (with much higher PCB concentrations than SDB sediment) prepared from a New Bedford Harbor (MA, USA) sediment. The toxic effects as measured by the growth rates in L. pictus were likely attributable to polycyclic aromatic hydrocarbons (PAHs), which were elevated in SDB sediment (7.3 microg/g), rather than PCBs.

Animals↗