@article {275, title = {Emerging investigator series: nontargeted screening of aryl hydrocarbon receptor agonists in endangered beluga whales from the St. Lawrence Estuary: beyond legacy contaminants.}, journal = {Environ Sci Process Impacts}, volume = {26}, year = {2024}, month = {2024 Sep 18}, pages = {1451-1464}, abstract = {

The elevated concentrations of organohalogen contaminants in the endangered St. Lawrence Estuary (SLE) belugas have prompted the hypothesis that aryl hydrocarbon receptor (AhR) activity may be a contributor towards their potential adverse effects. While indirect associations between AhR and contaminant levels have been reported in SLE beluga tissues, AhR activity was never directly measured. Using bioassays and nontargeted analysis, this study contrasted AhR activity and agonist profiles between pooled tissue extracts of endangered SLE and non-threatened Arctic belugas. Tissue extracts of SLE belugas exhibited significantly higher overall AhR activity than that of Arctic belugas, with a 2000s SLE beluga liver extract exerting significantly higher activity than blubber extracts of SLE and Arctic belugas from the same time period. Contrary to our expectations, well-known AhR agonists detected by nontargeted analysis, including polychlorinated biphenyls (PCBs), were only minor contributors to the observed AhR activity. Instead, Tox21 suspect screening identified more polar chemicals, such as dyes and natural indoles, as potential contributors. Notably, the natural product bromoindole was selectively detected in SLE beluga liver at high abundance and was further confirmed as an AhR agonist. These findings highlighted the significance of the AhR-mediated toxicity pathway in belugas and underscored the importance of novel AhR agonists, particularly polar compounds, in its induction.

}, keywords = {Animals, Beluga Whale, Endangered Species, Environmental Monitoring, Estuaries, Liver, Polychlorinated Biphenyls, Receptors, Aryl Hydrocarbon, Water Pollutants, Chemical}, issn = {2050-7895}, doi = {10.1039/d4em00243a}, author = {Barrett, Holly and Sun, Jianxian and Chen, Yuhao and Yang, Diwen and Verreault, Jonathan and Houde, Magali and Wania, Frank and Peng, Hui} } @article {269, title = {Identification of environmental and methodological factors driving variability of Pepper Mild Mottle Virus (PMMoV) across three wastewater treatment plants in the City of Toronto.}, journal = {Sci Total Environ}, volume = {932}, year = {2024}, month = {2024 Jul 01}, pages = {172917}, abstract = {

PMMoV has been widely used to normalize the concentration of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA, influenza, and respiratory syncytial virus (RSV) to account for variations in the fecal content of wastewater. PMMoV is also used as an internal RNA recovery control for wastewater-based epidemiology (WBE) tests. While potentially useful for the interpretation of WBE data, previous studies have suggested that PMMoV concentration can be affected by various physico-chemical characteristics of wastewater. There is also the possibility that laboratory methods, particularly the variability in centrifugation steps to remove supernatant from pellets can cause PMMoV variability. The goal of this study is to improve our understanding of the main drivers of PMMoV variability by assessing the relationship between PMMoV concentration, the physico-chemical characteristics of wastewater, and the methodological approach for concentrating wastewater samples. We analyzed 24-hour composite wastewater samples collected from the influent stream of three wastewater treatment plants (WWTPs) located in the City of Toronto, Ontario, Canada. Samples were collected 3 to 5 times per week starting from the beginning of March 2021 to mid-July 2023. The influent flow rate was used to partition the data into wet and dry weather conditions. Physico-chemical characteristics (e.g., total suspended solids (TSS), biological oxygen demand (BOD), alkalinity, electrical conductivity (EC), and ammonia (NH)) of the raw wastewater were measured, and PMMoV was quantified. Spatial and temporal variability of PMMoV was observed throughout the study period. PMMoV concentration was significantly higher during dry weather conditions. Multiple linear regression analysis demonstrates that the number and type of physico-chemical parameters that drive PMMoV variability are site-specific, but overall BOD and alkalinity were the most important predictors. Differences in PMMoV concentration for a single WWTP between two different laboratory methods, along with a weak correlation between pellet mass and TSS using one method may indicate that differences in sample concentration and subjective subsampling bias could alter viral recovery and introduce variability to the data.

}, keywords = {Environmental Monitoring, Ontario, Tobamovirus, Waste Disposal, Fluid, Wastewater}, issn = {1879-1026}, doi = {10.1016/j.scitotenv.2024.172917}, author = {Goitom, Eyerusalem and Ariano, Sarah and Gilbride, Kim and Yang, Minqing Ivy and Edwards, Elizabeth A and Peng, Hui and Dannah, Nora and Farahbakhsh, Farnaz and Hataley, Eden and Sarvi, Hooman and Sun, Jianxian and Waseem, Hassan and Oswald, Claire} } @article {86, title = {Current and historical concentrations of poly and perfluorinated compounds in sediments of the northern Great Lakes - Superior, Huron, and Michigan.}, journal = {Environ Pollut}, volume = {236}, year = {2018}, month = {2018 May}, pages = {373-381}, abstract = {

Current and historical concentrations of 22 poly- and perfluorinated compounds (PFASs) in sediment collected from Lake Superior and northern Lake Michigan in 2011 and Lake Huron in 2012 are reported. The sampling was performed in two ways, Ponar grabs of surface sediments for current spatial distribution across the lake and dated cores for multi-decadal temporal trends. Mean concentrations of the sum of PFASs (∑PFASs) were 1.5, 4.6 and 3.1 ng g dry mas (dm) in surface sediments for Lakes Superior, Michigan and Huron, respectively. Of the five Laurentian Lakes, the watersheds of Superior and Huron are the less densely populated by humans, and concentrations observed were typically less and from more diffuse sources, due to lesser urbanization and industrialization. However, some regions of greater concentrations were observed and might indicate more local, point sources. In core samples concentrations ranged from 7 that include perfluoro-n-octane sulfonate (PFOS) bind more strongly to sediment, which resulted in more accurate analyses of temporal trends. Shorter-chain PFASs, such as perfluoro-n-butanoic acid which is the primary replacement for C8 PFASs that have been phased out, are more soluble and were identified in some core layers at depths corresponding to pre-production periods. Thus, analyses of temporal trends of these more soluble compounds in cores of sediments were less accurate. Total elemental fluorine (TF) and extractable organic fluorine (EOF) indicated that identified PFASs were not a significant fraction of fluorine containing compounds in sediment (\<0.01\% in EOF).

}, keywords = {Environmental Monitoring, Fluorocarbons, Geologic Sediments, Great Lakes Region, Lakes, Water Pollutants, Chemical}, issn = {1873-6424}, doi = {10.1016/j.envpol.2018.01.065}, author = {Codling, Garry and Hosseini, Soheil and Corcoran, Margaret B and Bonina, Solidea and Lin, Tian and Li, An and Sturchio, Neil C and Rockne, Karl J and Ji, Kyunghee and Peng, Hui and Giesy, John P} } @article {88, title = {Simultaneous determination of (N-ethyl perfluorooctanesulfonamido ethanol)-based phosphate diester and triester and their biotransformation to perfluorooctanesulfonate in freshwater sediments.}, journal = {Environ Pollut}, volume = {234}, year = {2018}, month = {2018 Mar}, pages = {821-829}, abstract = {

While (N-ethyl perfluorooctanesulfonamido ethanol)-based phosphates (SAmPAPs) have been proposed as a group of perfluorooctanesulfonate (PFOS) precursors, investigation of their occurrence and fate has been limited to SAmPAP diester. In this study, SAmPAP diester and triester were simultaneously determined in freshwater sediment from Taihu Lake using a newly developed UPLC-MS/MS method, and their biotransformation to PFOS in lake sediment was investigated. SAmPAP diester and triester were detected in sediments with a detection frequency of 56\% and 88\%, and their mean concentrations were 0.24\ {\textpm}\ 0.11\ ng/g dry weight (dw) and 0.12\ {\textpm}\ 0.03\ ng/g dw, respectively. The SAmPAP diester/triester ratio in sediment was 1.1\ {\textpm}\ 4.2, much lower than that (6.7) observed in the technical product, and the positive correlation was found between the concentrations of SAmPAP diester and PFOS in sediments (r\ =\ 0.45, p\ =\ 0.01), suggesting that SAmPAP diester would be biotransformed to PFOS in the lake sediment. The microbial degradation test in the lake sediments further clarified that SAmPAP diester was biodegraded to PFOS, but SAmPAP triester was highly recalcitrant to microbial degradation. This study suggests that the occurrence of SAmPAP diester in freshwater lake sediments may be an important precursor of PFOS.

}, keywords = {Alkanesulfonic Acids, Bacteria, Biodegradation, Environmental, Biotransformation, China, Environmental Monitoring, Fluorocarbons, Geologic Sediments, Hydrocarbons, Fluorinated, Lakes, Organophosphates, Sulfonamides, Tandem Mass Spectrometry, Water Pollutants, Chemical}, issn = {1873-6424}, doi = {10.1016/j.envpol.2017.12.021}, author = {Zhang, Shiyi and Peng, Hui and Mu, Di and Zhao, Haoqi and Hu, Jianying} } @article {92, title = {Hydroxylated 2-Ethylhexyl tetrabromobenzoate isomers in house dust and their agonistic potencies with several nuclear receptors.}, journal = {Environ Pollut}, volume = {227}, year = {2017}, month = {2017 Aug}, pages = {578-586}, abstract = {

In the current study, by combining ultra-high resolution (UHR) MS spectra, MS spectra, and derivatization, three hydroxylated isomers of 2-ethylhexyl tetrabromobenzoate (OH-TBB) were identified in Firemaster 550 and BZ-54 technical products. Also, a new LC-UHRMS method, using atmospheric pressure chemical ionization (APCI), was developed for simultaneous analysis of OH-TBB, TBB, hydroxylated bis(2-ethylhexyl)-tetrabromophthalate (OH-TBPH) and TBPH in 23 samples of dust collected from houses in Saskatoon, SK, Canada. OH-TBBs were detected in 91\% of samples, with a geometric mean concentration of 0.21\ ng/g, which was slightly less than those of OH-TBPH (0.35\ ng/g). TBB was detected in 100\% of samples of dust with a geometric mean concentration of 992\ ng/g. Significant (p\ \<\ 0.001) log-linear relationships between concentrations of OH-TBBs, TBB, or OH-TBPHs and TBPH in dust support the hypothesis of a common source of these compounds. OH-TBBs were found to be strong agonists of peroxisome proliferator-activated receptor gamma (PPARγ) and weaker agonists of the estrogen receptor (ER), but no agonistic potencies was observed with the androgen receptor (AR). Occurrence of OH-TBBs in technical products and house dust, together with their relatively strong PPARγ potencies, indicated their potential risk to health of humans.

}, keywords = {Air Pollution, Indoor, Bromobenzoates, Canada, Dust, Environmental Monitoring, Flame Retardants, Halogenated Diphenyl Ethers, Humans}, issn = {1873-6424}, doi = {10.1016/j.envpol.2017.04.094}, author = {Peng, Hui and Sun, Jianxian and Saunders, David M V and Codling, Garry and Wiseman, Steve and Jones, Paul D and Giesy, John P} } @article {103, title = {Untargeted Screening and Distribution of Organo-Bromine Compounds in Sediments of Lake Michigan.}, journal = {Environ Sci Technol}, volume = {50}, year = {2016}, month = {2016 Jan 05}, pages = {321-30}, abstract = {

Previously unreported natural and synthetic organo-bromine compounds (NSOBCs) have been found to contribute more than 99\% of total organic bromine (TOB) in environmental matrices. We recently developed a novel untargeted method (data-independent precursor isolation and characteristic fragment, DIPIC-Frag) and identified \~{}2000 NSOBCs in two sediments from Lake Michigan. In this study, this method was used to investigate the distributions of these NSOBCs in 23 surficial samples and 24 segments of a sediment core from Lake Michigan. NSOBCs were detected in all 23 surficial samples and exhibited 10- to 100-fold variations in peak abundance among locations. The pattern of distributions of NSOBCs was correlated with depth of the water column (r(2) = 0.61, p \< 0.001). Hierarchical cluster analysis showed that sediments in close proximity exhibited similar profiles of NSOBCs. Distributions of NSOBCs in 24 segments of a sediment core dated from 1766 to 2008 were investigated, and samples from similar depths exhibited similar profiles of NSOBCs. NSOBCs were grouped into four clusters (soft-cluster analysis) with different temporal trends of abundances. 515 and 768 of the NSOBCs were grouped into cluster 1 and cluster 3 with increasing temporal trends, especially since 1950, indicating that abundances of these compounds might have been affected by human activities.

}, keywords = {Bromine Compounds, Environmental Monitoring, Geologic Sediments, Halogenated Diphenyl Ethers, Hydrocarbons, Brominated, Lakes, Michigan, Water Pollutants, Chemical}, issn = {1520-5851}, doi = {10.1021/acs.est.5b04709}, author = {Peng, Hui and Chen, Chunli and Cantin, Jenna and Saunders, David M V and Sun, Jianxian and Tang, Song and Codling, Garry and Hecker, Markus and Wiseman, Steve and Jones, Paul D and Li, An and Rockne, Karl J and Sturchio, Neil C and Giesy, John P} } @article {108, title = {Isomer-specific trophic transfer of perfluorocarboxylic acids in the marine food web of Liaodong Bay, North China.}, journal = {Environ Sci Technol}, volume = {49}, year = {2015}, month = {2015 Feb 03}, pages = {1453-61}, abstract = {

Trophic transfers of perfluorocarboxylic acids (PFCAs) have been well studied in aquatic food webs; however, most studies examined PFCAs as single compounds without differentiating isomers. In this study, an in-port derivatization GC-MS method was used to determine PFCA (perfluorooctanoic acid, PFOA; perfluorononanoic acid, PFNA; perfluorodecanoate acid, PFDA; perfluoroundecanoate acid, PFUnDA; perfluorododecanoate acid, PFDoDA; perfluorotridecanoate acid, PFTriDA, and perfluorotetradecanoate acid, PFTeDA) structural isomers in 11 marine species including benthic invertebrates, fishes, and gulls collected in November 2006 from Liaodong Bay in China. The total concentrations of linear PFCAs were 0.35-1.10, 0.93-2.61, and 2.13-2.69 ng/g ww, and the corresponding percentages of branched PFCAs to linear PFCAs were 6.6-15.5\%, 4.2-9.9\%, and 4.5-6.0\% in invertebrates, fishes, and birds, respectively. Except for linear PFOA, significant positive relationships were found between the concentrations of all the target linear PFCAs and trophic levels, and the trophic magnification factors (TMFs) ranged from 1.90 to 4.88. Positive correlations between the concentrations of branched PFCAs isomers and trophic levels were also observed but were without statistical significance. The relatively high biomagnification of linear isomers of PFCAs would lead to low percentages of branched PFCAs to total PFCAs in organisms at high trophic levels. This study for the first time clarified isomer-specific trophic transfers of PFCAs in a marine food web.

}, keywords = {Animals, Bays, Birds, Carboxylic Acids, China, Environmental Monitoring, Fishes, Fluorocarbons, Food Chain, Invertebrates, Isomerism, Water Pollutants, Chemical}, issn = {1520-5851}, doi = {10.1021/es504445x}, author = {Zhang, Zhong and Peng, Hui and Wan, Yi and Hu, Jianying} } @article {106, title = {Levels of Phthalate Metabolites in Urine of Pregnant Women and Risk of Clinical Pregnancy Loss.}, journal = {Environ Sci Technol}, volume = {49}, year = {2015}, month = {2015 Sep 01}, pages = {10651-7}, abstract = {

Toxicological studies have shown that phthalate esters (PAEs), a class of widely used and environmentally prevalent chemicals, can increase the abortion rate in animals, but epidemiological evidence is scarce. This study aimed to explore the relationship between the urinary concentration of phthalate metabolites and the risk of clinical pregnancy loss. A total of 132 women who underwent clinical pregnancy loss (cases) and 172 healthy pregnant women (controls) were recruited from Beijing, China. Eight phthalate metabolites in urine were determined by ultraperformance liquid chromatography tandem mass spectrometry (UPLC-MS/MS). Five phthalate metabolites, monomethyl phthalate (MMP), monoethyl phthalate (MEP), monoisobutyl phthalate (MiBP), mono-n-butyl phthalate (MnBP), and mono(2-ethlyhexyl) phthalate (MEHP), were detected in at least 95\% of the urine samples, with the highest median concentration of 51.0 μg/g of creatinine for MnBP of all participants. The differences in urinary concentrations of phthalate metabolites between cases and controls were evaluated using the Mann-Whitney U test. The concentrations of MEP (median of 18.7 μg/g of creatinine), MiBP (23.3 μg/g of creatinine), and MnBP (58.2 μg/g of creatinine) detected in the cases were significantly higher than those (15.7 μg/g of creatinine for MEP, 19.4 μg/g of creatinine for MiBP, and 43.9 μg/g of creatinine for MnBP) in the controls (p \< 0.05). Increasing risks of clinical pregnancy loss were observed from the first to fourth quartiles of the MEP, MiBP, and MnBP concentrations (p \< 0.05 for trend). We concluded that exposure to MEP, MiBP, and MnBP was associated with an increased risk of clinical pregnancy loss.

}, keywords = {Adult, Beijing, Case-Control Studies, Embryo Loss, Environmental Monitoring, Esters, Female, Humans, Metabolome, Middle Aged, Odds Ratio, Phthalic Acids, Pregnancy, Risk Factors, Young Adult}, issn = {1520-5851}, doi = {10.1021/acs.est.5b02617}, author = {Mu, Di and Gao, Fumei and Fan, Zhanlan and Shen, Huan and Peng, Hui and Hu, Jianying} } @article {112, title = {Isomer-specific accumulation of perfluorooctanesulfonate from (N-ethyl perfluorooctanesulfonamido)ethanol-based phosphate diester in Japanese Medaka (Oryzias latipes).}, journal = {Environ Sci Technol}, volume = {48}, year = {2014}, month = {2014 Jan 21}, pages = {1058-66}, abstract = {

While (N-ethyl perfluorooctanesulfonamido)ethanol (FOSE) -based phosphate diester (diSPAP) has been proposed as a candidate precursor of perfluorooctanesulfonate (PFOS), its potential biotransformation to PFOS has not been verified. Metabolism of diSPAP was investigated in Japanese medaka ( Oryzias latipes ) after exposure in water for 10 days, followed by 10 days of depuration. Branched isomers of diSPAP (B-diSPAP) were preferentially enriched in medaka exposed to diSPAP, with the proportion of branched isomers (BF) ranging from 0.56 to 0.80, which was significantly greater than that in the water to which the medaka were exposed (0.36) (p \< 0.001). This enrichment was due primarily to preferential uptake of B-diSPAP. PFOS together with perfluorooctanesulfonamide (PFOSA), N-ethyl perfluorooctanesulfonamide (NEtFOSA), 2-(perfluorooctanesulfonamido)acetic acid (FOSAA), NEtFOSAA, FOSE, and NEtFOSE were detected in medaka exposed to diSPAP, which indicated the potential for biotransformation of diSPAP to PFOS via multiple intermediates. Due to preferential metabolism of branched isomers, FOSAA and PFOSA exhibited greater BF values (\>0.5) than those of NEtFOSA, NEtFOSAA, and NEtFOSE (\<0.2). Such preferential metabolism of branched isomers along the primary pathway of metabolism and preferential accumulation of B-diSPAP led to enrichment of branched PFOS (B-PFOS) in medaka. Enrichment of B-PFOS was greater for 3-, 4-, and 5-perfluoromethyl PFOS (P3MPFOS, P4MPFOS, and P5MPFOS), for which values of BF were 0.58 {\textpm} 0.07, 0.62 {\textpm} 0.06, and 0.61 {\textpm} 0.05 (day 6), respectively; these values are 5.8-, 7.8-, and 6.4-fold greater than those of technical PFOS. This work provides evidence on the isomer-specific accumulation of PFOS from diSPAP and will be helpful to track indirect sources of PFOS in the future.

}, keywords = {Alkanesulfonic Acids, Animals, Biotransformation, Chromatography, High Pressure Liquid, Environmental Monitoring, Esters, Fluorocarbons, Gas Chromatography-Mass Spectrometry, Half-Life, Hydrocarbons, Fluorinated, Isomerism, Kinetics, Metabolic Networks and Pathways, Organophosphorus Compounds, Oryzias, Phosphates, Reference Standards, Sulfonamides}, issn = {1520-5851}, doi = {10.1021/es404867w}, author = {Peng, Hui and Zhang, Shiyi and Sun, Jianxian and Zhang, Zhong and Giesy, John P and Hu, Jianying} } @article {110, title = {Occurrences of three classes of antibiotics in a natural river basin: association with antibiotic-resistant Escherichia coli.}, journal = {Environ Sci Technol}, volume = {48}, year = {2014}, month = {2014 Dec 16}, pages = {14317-25}, abstract = {

To investigate the occurrence of antibiotics in urban rivers and their association with antibiotic-resistant Escherichia coli, 20 (fluoro)quinolone antibiotics (FQs), 16 tetracycline antibiotics (TCs) and their degradation products, and 25 sulfonamides (SAs) and some degradation products were determined in 45 river samples and 13 discharged wastewater samples collected from Wenyu River and its tributaries and 4 composite effluent samples from sewage treatment plants in Beijing, China. Fifteen FQs, eight TCs, including four degradation chemicals, and sixteen SAs, including four acetylated products, were detected in the river water. The SAs were the dominant antibiotic (total concentrations up to 3164.0 ng/L) in river water, followed by FQs (1430.3 ng/L) and TCs (296.6 ng/L). The sum concentrations for each class of detected antibiotic in the 13 discharge site samples were higher than those in river samples, up to 12326.7 ng/L for SAs, 6589.2 ng/L for FQs, and 730.1 ng/L for TCs, largely contributing to the high concentrations in the river basin. Log-linear regression analysis confirmed that the concentrations of FQs, TCs, and SAs in the Wenyu River basin were strongly correlated with the number of E. coli resistant to FQs (p \< 0.05), TCs (p \< 0.05), and SAs (p \< 0.05), providing evidence for the environmental impacts of antibiotic usage.

}, keywords = {Anti-Bacterial Agents, China, Drug Resistance, Bacterial, Environmental Monitoring, Escherichia coli, Fluoroquinolones, Rivers, Sulfonamides, Tetracyclines, Waste Water, Water Pollutants, Chemical}, issn = {1520-5851}, doi = {10.1021/es503700j}, author = {Zhang, Qinqin and Jia, Ai and Wan, Yi and Liu, Hong and Wang, Kunping and Peng, Hui and Dong, Zhaomin and Hu, Jianying} } @article {111, title = {Trophic transfer of dechloranes in the marine food web of Liaodong Bay, north China.}, journal = {Environ Sci Technol}, volume = {48}, year = {2014}, month = {2014 May 20}, pages = {5458-66}, abstract = {

Dechloranes are of particular concern because of their ubiquity in environmental matrices, but little is known about their trophic transfer in aquatic food web. This study investigated the trophic transfer of seven dechloranes in a marine food web from Liaodong Bay, China. Dechloranes were determined in sediments and 15 marine species including benthic invertebrates, fish and gulls collected from Liaodong Bay. Biomagnification factors (BMFTL) of dechloranes in black-headed gulls were calculated to be 6.4, 1.7, 0.45, 0.36, 0.14, and 0.11 for mirex, Dechlorane 602 (Dec 602), Dechlorane 603 (Dec 603), antiundecachloropentacyclooctadecadiene (anti-Cl11DP), syn-dechlorane plus (syn-DP), and anti-DP. Significantly positive relationships were found between lipid equivalent concentrations of mirex, Dec 602, and anti-Cl11DP and trophic levels, and the trophic magnification factors (TMFs) were 13, 3.7, and 5.6, respectively, indicating that these compounds undergo trophic magnification in the aquatic food web. Lipid equivalent concentrations of Dec 603 and DP isomers did not exhibit a statistically significant correlation with trophic levels. The relatively low trophic magnification potentials of Dec 603 and DP isomers were possibly due to their extreme hydrophobicity (logKOW: 11.2-11.3) and subsequent low bioavailabilities compared with mirex (7.0), Dec 602 (8.1) and anti-Cl11DP. The results provided important information for understanding the ecological risk of dechloranes.

}, keywords = {Animals, Aquatic Organisms, Bays, Charadriiformes, China, Environmental Monitoring, Fishes, Food Chain, Geologic Sediments, Hydrocarbons, Chlorinated, Invertebrates, Ontario, Regression Analysis, Water Pollutants, Chemical}, issn = {1520-5851}, doi = {10.1021/es500229y}, author = {Peng, Hui and Wan, Yi and Zhang, Kun and Sun, Jianxian and Hu, Jianying} } @article {115, title = {Tissue distribution, maternal transfer, and age-related accumulation of dechloranes in Chinese sturgeon.}, journal = {Environ Sci Technol}, volume = {46}, year = {2012}, month = {2012 Sep 18}, pages = {9907-13}, abstract = {

While dechloranes have been detected in environmental media and wildlife, limited information was available on their tissue distribution in wildlife. Syn-dechlorane plus (syn-DP), anti-DP, syn-undecachloropentacyclooctadecadiene (syn-Cl(11)DP), anti-Cl(11)DP, dechlorane 602, dechlorane 603 and mirex were measured in 13 organs of 17 female Chinese sturgeon (Acipenser sinensis). Dechloranes were detected in all tissues and the highest concentrations of total dechloranes were detected in heart (87 pg/g ww, 4.5-645 pg/g ww), followed by adipose (61 pg/g ww, 14-531 pg/g ww) and eggs (57 pg/g ww, 13-261 pg/g ww). The tissue distribution of DP was mainly determined by lipid partition, while Dec 602 and Dec 603 preferred to accumulate in the intestine and stomach. The values of f(anti) (the concentration of anti-DP relative to the sum concentration of DP) in maternal tissues (0.72 {\textpm} 0.03 in muscle) were significantly higher than those found in eggs (0.65 {\textpm} 0.04) (p \< 0.001), while f(anti-Cl11DP) (the concentration of anti-Cl(11)DP relative to the sum concentration of Cl(11)DP) in maternal tissues (0.59 {\textpm} 0.10 in muscle) was significantly lower than that in eggs (0.75 {\textpm} 0.13) (p \< 0.05). High maternal transfer efficiencies of dechloranes were observed in eggs, which accounted for 49\% of the total body burden, and the ratios of concentrations in eggs to maternal tissues (EMR) for mirex, Dec 602, Dec 603, syn-Cl(11)DP, anti-Cl(11)DP, syn-DP, and anti-DP were 18, 8.8, 5.2, 2.6, 5.2, 5.5 and 3.7, respectively, which are dependent on their K(OW) values (r = -0.66, p \< 0.01). Negative age-related trends were observed for mirex, Dec 603, syn-Cl(11)DP and anti-Cl(11)DP in eggs (R(2) = 0.28-0.38, p = 0.02-0.05), which were possibly due to their high transfer efficiencies to eggs from maternal body (49\%).

}, keywords = {Animals, China, Eggs, Environmental Monitoring, Female, Fishes, Flame Retardants, Hydrocarbons, Chlorinated, Polycyclic Compounds, Tissue Distribution, Water Pollutants, Chemical}, issn = {1520-5851}, doi = {10.1021/es3025879}, author = {Peng, Hui and Zhang, Kun and Wan, Yi and Hu, Jianying} } @article {117, title = {Occurrence and source apportionment of sulfonamides and their metabolites in Liaodong Bay and the adjacent Liao River basin, North China.}, journal = {Environ Toxicol Chem}, volume = {30}, year = {2011}, month = {2011 Jun}, pages = {1252-60}, abstract = {

The presence of antibiotics in the environment is of great concern because of their potential for resistance selection among pathogens. In the present study we investigated the occurrence of 19 sulfonamides, five N-acetylated sulfonamide metabolites, and trimethoprim in the Liao River basin and adjacent Liaodong Bay, China, as well as 10 human/agricultural source samples. Within the 35 river samples, 12 sulfonamides, four acetylated sulfonamides, and trimethoprim were detected, with the dominant being sulfamethoxazole (66.6 ng/L), N-acetylsulfamethoxazole (63.1 ng/L), trimethoprim (29.0 ng/L), sulfadiazine (14.0 ng/L), and sulfamonomethoxine (8.4 ng/L); within the 36 marine samples, 10 chemicals were detected, with the main contributions from sulfamethoxazole (25.2 ng/L) and N-acetylsulfamethoxazole (28.6 ng/L). Sulfamethoxazole (25.9\%), N-acetylsulfamethoxazole (46.6\%), trimethoprim (22.9\%), and sulfapyridine (1.4\%) were the main chemicals from human sources, while sulfamonomethoxine, sulfamethazine, sulfaquinoxaline, sulfaguanidine, sulfadiazine, sulfanilamide, and sulfamethoxypyridazine were dominant in the animal husbandry sources, specifically, swine and poultry farms, and sulfamethoxazole (91\%) was dominant in the mariculture source. A principal component analysis with multiple linear regression was performed to evaluate the source apportionment of total sulfonamides in Liaodong Bay. It was found that animal husbandry contributed 15.2\% of total sulfonamides, while human sources contributed 28.5\%, and combined human and mariculture sources contributed 56.3\%. In addition, the mariculture contribution was 24.1\% of total sulfonamides into the sea based on mass flux estimation. The present study is the first report that the environmental levels of sulfonamide metabolites were comparable to the corresponding parents; therefore, we should pay attention to their environmental occurrence. Source apportionment showed human discharge (60.7\%) significantly contributed to these antibiotics in Liaodong Bay, which provides important information for environmental management.

}, keywords = {Agriculture, Anti-Bacterial Agents, Aquaculture, China, Environmental Monitoring, Humans, Linear Models, Principal Component Analysis, Rivers, Seawater, Spectrometry, Mass, Electrospray Ionization, Sulfamethazine, Sulfamethoxazole, Sulfamethoxypyridazine, Sulfamonomethoxine, Sulfapyridine, Sulfaquinoxaline, Sulfonamides, Tandem Mass Spectrometry, Trimethoprim, Water Pollutants, Chemical, Water Pollution, Chemical}, issn = {1552-8618}, doi = {10.1002/etc.508}, author = {Jia, Ai and Hu, Jianying and Wu, Xiaoqin and Peng, Hui and Wu, Shimin and Dong, Zhaomin} }