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This study utilized both conventional molecular analysis and compound-specific isotopic techniques to identify the sources of polycyclic aromatic hydrocarbons (PAHs) in sediments of Ulsan Bay, South Korea. The concentrations of 15 traditional and 11 emerging PAHs were determined in sediments from 21 source sites and 26 bay sites. The concentrations and compositions of traditional and emerging PAHs varied significantly, even at sites close to the source areas. The results obtained from diagnostic ratios and the positive matrix factorization model for source identification were inconsistent in adjacent source areas. The δ13C profiles of PAHs, such as phenanthrene (Phe), fluoranthene (Fl), pyrene (Py), and benz[ a ]anthracene (BaA) in the sediments showed distinct features depending on the surrounding sources. In urban sediments, lighter δ13C Phe values were observed (mean: −25.1‰), whereas relatively heavier values of δ13C Py were found in petroleum industry areas (mean: −23.4‰). The Bayesian isotope mixing model indicates that the predominant source of PAHs in Ulsan Bay sediments was the petroleum industry (45%), followed by the non-ferrous metals industry (30%), automobile industry (18%), and urban areas (6.3%). These results demonstrated the utility of stable isotopes in assessing the sources and contributions of PAHs in small-scale regions. However, there are still limitations in compound-specific isotope analysis of PAHs, including insufficient end-members for each source, difficulty in analysis, and the influence of non-point sources; thus, further study is needed to expand its application. [Display omitted] • Molecular and isotopic indicators were used to trace the origin of sedimentary PAHs. • Source identification of PAHs based on molecular composition was inaccurate. • δ13C values of individual PAHs exhibited distinct features according to their sources. • Petroleum and non-ferrous metals industries were major contributors of PAHs. [ABSTRACT FROM AUTHOR]

In the late 1990s, severe pollution by persistent organic contaminants (POCs) was observed in Lake Sihwa by use of a combination of instrumental analyses and in vitro bioassays. To determine long-term changes (>15-year gaps) in distributions of POCs and their potential toxic potencies in the given region, sediment assessments were reconducted. Target chemicals include polycyclic aromatic hydrocarbons (PAHs), alkylphenols (APs), and recently reported emerging chemicals, styrene oligomers (SOs). We employed in vitro bioassays (such as H4IIE- luc and MVLN) to determine potential sediment toxicities. The reduction rates of mean concentrations of APs and SOs in sediments between the two sampling years (1998 vs. 2015) were estimated to be 99% and 67%, respectively. Although APs and SOs significantly declined over the 15-year period, concentrations of PAHs were consistent. Results of the bioassays were consistent with the instrumental data, with relatively great concentrations of all target compounds being detected, particularly in inland creeks. Compositions of all target compounds exhibited changes in homologue patterns over the 15 years considered. This result indicated varying and/or continuing sources in this region. In particular, PAHs were dominated by higher-molecular-weight PAHs (e.g., benzo[ g,h,i ]perylene and benzo[ b ]fluoranthene) in recent years. This result might indicate consumption of oil-related fuels. Quantitative potency balance analysis revealed that concentrations of instrumentally-derived equivalents accounted for as little as 18.5% of bioassay-derived equivalents, which indicated significant amounts of unknown and/or unmeasured compounds were present. The present study documented the continuing severe pollution by selected POCs in the Lake Sihwa region over the last 15 years, indicating a lack of management in the area studied. [ABSTRACT FROM AUTHOR]

Distribution and sources of polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) in the glacimarine sediments (35 sites) of Svalbard were investigated. PCBs (32 congeners), traditional PAHs (15 homologs), emerging PAHs (11 homologs), and alkylated PAHs (16 homologs) were widely distributed in the Svalbard sediments (ranges: below method detection limit to 20, 21 to 3600, 1.0 to 1400, and 31 to 15,000 ng g−1 dry weight, respectively). Compositional analysis indicated that PCBs mainly originated from combustion sources, with PAHs being strongly influenced by local sources. Positive matrix factorization analysis showed that PAHs were associated with vehicle and petroleum combustion, coal, and coal combustion. Coal-derived PAHs contributed significantly to the sediments of Van Mijenfjorden. Remnants of coal mining activity trapped in the permafrost appear to enter the coastal environments as ground ice melts. Consequently, PAHs are currently emerging as the most significant contributors to potential risks in the Svalbard ecosystems. [Display omitted] • Distributions of PCBs and PAHs in the sediments of Arctic Svalbard were investigated. • Hornsund and Van Mijenfjorden showed relatively high concentrations of PAHs. • PAHs in Svalbard sediments mainly originated from local coal and petrogenic sources. • PAHs contributed greatly to the potential ecological risks of sediments in Svalbard. [ABSTRACT FROM AUTHOR]

Effect-directed analysis (EDA) was performed to identify the major aryl hydrocarbon receptor (AhR) agonists in sediments collected from a highly industrialized area (Lake Shihwa, Korea). Great AhR-mediated potencies were found in fractions containing aromatic compounds with log K ow values of 5–8, and relatively great concentrations of styrene oligomers (SOs) and polycyclic aromatic hydrocarbons (PAHs) were detected in those fractions. Until now, there was little information on occurrences and toxic relative potencies (RePs) of SOs in coastal environments. In the present study; i) distributions and compositions, ii) AhR binding affinities, and iii) contributions of SOs to total AhR-mediated potencies were determined in coastal sediments. Elevated concentrations of 10 SOs were detected in sediments of inland creeks ranging from 61 to 740 ng g −1 dry mass (dm), while lesser concentrations were found in inner (mean = 33 ng g −1 dm) and outer regions (mean = 25 ng g −1 dm) of the lake. Concentrations of PAHs in sediments were comparable to those of SOs. 2,4-diphenyl-1-butene (SD3) was the predominant SO analogue in sediments. SOs and PAHs were accumulated in sediments near sources, and could not be transported to remote regions due to their hydrophobicity. RePs of 3 SOs could be derived, which were 1000- to 10,000-fold less than that of one representative potent AhR active PAH, benzo[ a ]pyrene. Although concentrations of SOs in sediments were comparable to those of PAHs, the collective contribution of SOs to total AhR-mediated potencies were rather small (<1%), primarily due to their smaller RePs. Overall, the present study provides information on distributions and AhR binding affinities for SOs as baseline data for degradation products of polystyrene plastic in the coastal environment. [ABSTRACT FROM AUTHOR]

Novel aryl hydrocarbon receptor (AhR) agonists were identified in coastal sediments in the Yellow and Bohai Seas by use of a combination of effect-directed analysis (EDA) and in silico prediction. A total of 125 sediments were screened for AhR-mediated potencies using H4IIE- luc bioassay. Great potencies were observed in organic extracts, mid-polar fraction (F2), and subfractions of F2 (F2.6–F2.9) of sediments collected from Nantong, Qinhuangdao, and Yancheng. Less than 15% AhR potencies could be explained by detected dioxin-like PAHs. Full-scan screening analysis was conducted for the more potent fractions using GC-QTOFMS to investigate the presence of unmonitored AhR agonists. A five-step prioritization strategy was applied; 92 candidate compounds satisfied all criteria. Among these chemicals, thirteen were evaluated for AhR efficacy. Six compounds; benz[ b ]anthracene, 6-methylchrysene, 2-methylbenz[ a ]anthracene, 1-methylbenz[ a ]anthracene, 1,12-dimethylbenzo[ c ]phenanthrene, and indeno[1,2,3- cd ]fluoranthene, exhibited significant AhR-mediated efficacies. 1,12-dimethylbenzo[ c ]phenanthrene and indeno[1,2,3- cd ]fluoranthene were identified as novel AhR agonists. Potency balance analysis showed that the six newly identified AhR agonists explained 0.4–100% of the total AhR-mediated potencies determined. Overall, combining EDA and in silico prediction applied in this study demonstrated the benefits of assessing the potential toxic effects of previously unidentified AhR agonists in sediments from the coasts of China and Korea. [Display omitted] • AhR potencies in sediments from the Yellow and Bohai Seas at large scale were evaluated. • Unmonitored AhR-active compounds in sediments identified using advanced EDA. • DBcP and IcdF were identified as novel AhR agonists in sediments. • Assay-specific relative potency values were obtained for dominant AhR agonists. [ABSTRACT FROM AUTHOR]

Potential toxicants in sediments collected from an industrialized bay of Korea were identified by use of effect-directed analysis (EDA). Three marine microalgal bioassays (Dunaliella tertiolecta , Isochrysis galbana , and Phaeodactylum tricornutum) with diverse endpoints were employed. Initial screening of raw organic extracts of sediments indicated large variations among locations and species in a traditional endpoint "inhibition of growth". After fractionation, inhibition of growths increased significantly, particularly in some fractions containing aromatics with log K OW 5−6 (F2.6). While viabilities of cells were adversely affected in more fractions, including F2.6−F2.7 (log K OW 5−7) and F3.5−F3.6 (log K OW 4–6). Among the several endpoints of viability, esterase activity seemed to be more sensitive, followed by integrity of cell membranes, chlorophyll a , cell size, and intracellular complexity. Instrumental analyses indicated that toxicities to microalgae observed in F2.7 could not be fully explained by target PAHs. Full-scan screening analysis using GC-QTOFMS identified 58 compounds in F2.7 with matching scores ≥90%. Based on toxic potencies for these compounds predicted by ECOSAR, several causative agents, including 1-phenylpyrene, dibenz[ a , c ]anthracene, and picene were suggested. Overall, viability of microalgae provided sensitive and high-resolution toxicity screening of samples into integrative assessment of sediment. ga1 • Potential microalgal toxicants in sediments were identified by effects-directed analysis. • Three marine microalgal bioassays were utilized with a sensitive cell viability analysis. • Inhibitions of microalgal growth were observed for fractions of aromatics with log K OW 5–6. • Esterase activity was more sensitive, followed by cell membrane integrity and Chl. a. • 1-Phenylpyrene, dibenz[ a , c ]anthracene, and picene were found to be causative agents. [ABSTRACT FROM AUTHOR]

Contamination status of traditional and emerging persistent toxic substances (PTSs) in sediments and their major sources were investigated in Ulsan Bay, Korea. A total of 47 PTSs, including 15 traditional PAHs, ten styrene oligomers (SOs), six alkylphenols (APs), and 16 emerging PAHs (E-PAHs) were analyzed. Concentrations of traditional PAHs, SOs, and APs ranged from 35 to 1300 ng g−1 dry weight (dw), 30 to 3800 ng g−1 dw, and 30 to 430 ng g−1 dw, respectively. For the last 20 years, PTSs contamination in the bay area has been improved. However, 12 E-PAHs were widely detected in sediments, with a maximum of 240 ng g−1 dw (for benzo[ e ]pyrene) at the creek site. These E-PAHs seemed to originate from surrounding activities, such as biomass combustion, mobile sources, and diesel combustion. Due to environmental concerns for E-PAHs, further research on the potential toxicity, distribution, and behavior of these compounds should be implemented. Unlabelled Image • Contamination levels of PTSs in sediments have decreased during the last decades. • The major source of PAHs has changed from petroleum sources to combustion origins. • E-PAHs were widely distributed in the sediments, originating from surrounding activity. • E-PAHs have some potential toxicity; thus, further research should be implemented. [ABSTRACT FROM AUTHOR]

• We first address the recovery timeline of the HSOS by 10-years monitoring dataset. • Concentrations of residual oils in the environments rapidly dropped to background levels. • Recovery of benthic ecosystem was evaluated based on the number of species and H′. • Damaged benthic communities were fully recovered after ~6 years. • The high tidal mixing and intensive initial cleanup might have contributed to rapid recovery. The 2007 Hebei Spirit oil spill (HSOS), the largest in the national history, has negatively impacted the entire environment and ecosystem along the west coast of South Korea. Although many studies have reported the damages and impacts from the HSOS, quantitative assessment evaluating the recovery time and status have not been documented. Here, we first address the recovery timeline of the HSOS, by comprehensive analyses of 10-years accumulated data in quantitative manner. Concentrations of residual oils in seawater, sediments, and oysters rapidly dropped to backgrounds in 16, 75, and 33 months, respectively. Also, damaged benthic communities of intertidal and subtidal areas were fully recovered only after ~6 years. The present results collectively indicated unexpectedly fast recovery of the damaged environment and ecosystem from such a huge oil spill. The high tidal mixing (~9 m tidal height) and intensive human cleanup (~1.2 million volunteers) at the initial cleanup period might have contributed to rapid recovery; cf. 4–5 times faster than the Exxon Valdez oil spill. However, potential risk to human health remains unclear. Thus, it is warranted to conduct more in depth epidemiological studies to address chronic health effects associated with the cleanup volunteers as well as the local residents who have been living nearby the oil spill impacted sites. [ABSTRACT FROM AUTHOR]

For decades, in response to industrialization and urbanization, environmental qualities of estuarine and coastal areas of the west coast of Korea have been deteriorating. Long-term changes in concentrations of persistent toxic substances (PTSs) in sediments, including PAHs, styrene oligomers, nonylphenols, and metals and their potential toxicities via AhR- and ER-mediated potencies, and bioluminescent bacterial inhibition, were investigated. Long-term monitoring in five estuarine and coastal areas (2010–2018; 10 sites) showed that concentrations of PAHs and nonylphenols in sediments have declined while concentrations of some metals, Cd, Cr, and Hg have increased. Similarly, AhR-mediated potencies in sediments have declined, but inhibitions of bioluminescent bacteria have increased. Concentrations of sedimentary PAHs and AhR-mediated potencies were significantly (p < 0.01) and positively correlated. Sources of PAHs from combustion have been gradually declining while inputs from vehicle exhaust by-products have been increasing. Overall, this study brought our attention a balanced regulation in chemical-specific manner. Unlabelled Image • We investigated long-term trends (2010–2018) of PTSs and potential toxicities in sediments. • Concentrations of PAHs and nonylphenols in sediments have been declining since 2010. • Concentrations of Cd, Cr, and Hg are now increasing in sediments of the west coast of Korea. • AhR-mediated potencies have declined, while inhibitions of bioluminescent are increasing. • Long-term assessment indicated a balanced environmental regulation for PTSs management. [ABSTRACT FROM AUTHOR]

• EDA combined with FSA identified unknown toxicants in industrial sediments. • Benz[ b ]anthracene, 11H-benzo[ a ]fluorene, and 4,5-methanochrysene are novel AhR agonists. • Benz[ b ]anthracene showed 10-fold greater AhR potency compared to benzo[ a ]pyrene. • Newly identified AhR agonists significantly contributed to AhR potencies from sediments. This study utilized effect-directed analysis (EDA) combined with full-scan screening analysis (FSA) to identify aryl hydrocarbon receptor (AhR)-active compounds in sediments of inland creeks flowing into Lake Sihwa, South Korea. The specific objectives were to (i) investigate the major AhR-active fractions of organic extracts of sediments by using H4IIE- luc in vitro bioassay (4 h and 72 h exposures), (ii) quantify known AhR agonists, such as polycyclic aromatic hydrocarbons (PAHs) and styrene oligomers (SOs), (iii) identify unknown AhR agonists by use of gas chromatography-quadrupole time-of-flight mass spectrometry (GC-QTOFMS), and (iv) determine contributions of AhR agonists to total potencies measured by use of the bioassay. FSA was conducted on fractions F2.6 and F2.7 (aromatics with log K ow 5–7) in extracts of sediment from Siheung Creek (industrial area). Those fractions exhibited significant AhR-mediated potency as well as relatively great concentrations of PAHs and SOs. FSA detected 461 and 449 compounds in F2.6 and F2.7, respectively. Of these, five tentative candidates of AhR agonist were selected based on NIST library matching, aromatic structures and numbers of rings, and available standards. Benz[ b ]anthracene, 11H-benzo[ a ]fluorene, and 4,5-methanochrysene exhibited significant AhR-mediated potency in the H4IIE- luc bioassay, and relative potencies of these compounds were determined. Potency balance analysis demonstrated that these three newly identified AhR agonists explained 1.1% to 67% of total induced AhR-mediated potencies of samples, which were particularly great for industrial sediments. Follow-up studies on sources and ecotoxicological effects of these compounds in coastal environments would be required. [ABSTRACT FROM AUTHOR]

After the Gulf War Oil Spill, there have been many investigations about distributions of oil-derived pollutants nearby areas, but lacking in ecotoxicological assessment. We evaluated the potential toxicity of asphalt mats, sediments, and biota (polychaetes, chitons, snapping shrimps, and crabs) by combining two bioassays (H4IIE- luc and Vibrio fischeri) and in situ microbial community (eDNA). Samples were collected from Abu Ali Island, and organic extracts were bioassayed and further fractionated according to the chemical polarity using silica gel column. Great aryl hydrocarbon receptor (AhR)-mediated potencies and inhibition of bioluminescence were mainly found in aromatics (F2) and saturates (F1) fractions of asphalt mat and sediments, respectively, while great toxicological responses in biota samples were found in resins and polar (F3) fraction. We also confirmed that potential toxicities of biota were species-specific; great AhR-mediated potencies were found in polychaetes and great bioluminescence inhibitions were found in crabs. In microbial communities, most genera (up to 90%) were associated with polycyclic aromatic hydrocarbons (PAHs)-degrading bacteria, supporting that PAHs are the primary stressors of the benthic community around Abu Ali Island. The present study provides useful information on the contamination status, risk assessment of environmental matrices and benthic organisms in Abu Ali Island. Image 1 • Significant AhR-mediated potencies were found in sediments and polychaetes. • Polar fractions of biota extracts were responsible for luminescence inhibition. • Species diversity and composition of bacterial community affected by residual oils. • Up to 90% of genera of microbial community were associated with PAHs-degradation. [ABSTRACT FROM AUTHOR]

This study investigated the large-scale distributions of persistent toxic substances (PTSs) and heavy metals in sediments of the Yellow Sea, collected from six transects between latitudes 32 and 37 degrees north (n = 35). Elevated concentrations of polychlorinated biphenyls (PCBs) were detected near the mainland, with a predominance of low-chlorinated congeners (di to tetra, ∼60%), indicative of atmospheric deposition. Analysis of traditional and emerging polycyclic aromatic hydrocarbons (t-PAHs and e-PAHs) revealed notable enrichment in the Central Yellow Sea Mud Zone (CYSM), attributing fossil fuel combustion as the significant source. Styrene oligomers and alkylphenols exhibited notable accumulation near the Han River Estuary in South Korea and the Yangtze River Estuary in China, respectively. The accumulation of heavy metals was predominantly observed in the CYSM, with element-specific distribution patterns. Cluster analysis revealed distinct distribution patterns for PTSs and metals, highlighting their source-dependent and grain size-dependent behaviors. In addition, the distribution and accumulation of PTSs tended to depend on their partitioning coefficients, such as the octanol-air partition coefficient (log K OA) and octanol-water partition coefficient (log K OW). This study offers valuable insights into the sources, transport, and fate of hazardous substances in the Yellow Sea, emphasizing the necessity for targeted environmental management strategies. [Display omitted] • The distribution of PTSs and metals in sediments exhibited a compound-specific manner. • PCBs, styrene oligomers, and alkylphenols were accumulated near their sources. • PAHs, originating from fossil fuel combustion, mainly accumulated in CYSM. • Metals accumulated in CSYM similarly to PAHs and showed a grain size-dependent trend. • The fate of PTSs was dependent on partition coefficients, such as log K OW and log K OA. [ABSTRACT FROM AUTHOR]

The two popular source tracing tools of stable isotope ratios (δ 13 C and δ 15 N) and fluorescence spectroscopy were used to estimate the relative source contributions to sediment organic matter (SeOM) at five different river sites in an agricultural-forested watershed (Soyang Lake watershed), and their capabilities for the source assignment were compared. Bulk sediments were used for the stable isotopes, while alkaline extractable organic matter (AEOM) from sediments was used to obtain fluorescent indices for SeOM. Several source discrimination indices were fully compiled for a range of the SeOM sources distributed in the catchments of the watershed, which included soils, forest leaves, crop (C3 and C4) and riparian plants, periphyton, and organic fertilizers. The relative source contributions to the river sediment samples were estimated via end member mixing analysis (EMMA) based on several selected discrimination indices. The EMMA based on the isotopes demonstrated that all sediments were characterized by a medium to a high contribution of periphyton ranging from ~ 30% to 70% except for one site heavily affected by forest and agricultural fields with relatively high contributions of terrestrial materials. The EMMA based on fluorescence parameters, however, did not show similar results with low contributions from forest leaf and periphyton. The characteristics of the studied watershed were more consistent with the source contributions determined by the isotope ratios. The discrepancy in the EMMA capability for source assignments between the two analytical tools can be explained by the limited analytical window of fluorescence spectroscopy for non-fluorescent dissolved organic matter (FDOM) and the inability of AEOM to represent original bulk particulate organic matter (POM). [ABSTRACT FROM AUTHOR]

[Display omitted] • Microalgal bioassay with multiple endpoints was applied to the effect-directed analysis. • Great microalgal toxicity was induced in polar fractions of sediment extracts. • Cell viability was a more sensitive endpoint compared to growth inhibition. • Nitrophenols were newly identified as microalgal toxicants in sediments. • Newly identified toxicants did not fully explain the induced toxicities of microalgae. Microalgal toxicants in sediments from an industrialized area (Ulsan Bay) in South Korea were identified using effect-directed analysis (EDA) with full-scan screening analysis (FSA) and microalgal bioassays with multiple endpoints. The growth rate and cell viability of three microalgae (Isochrysis galbana , Dunaliella tertiolecta , and Phaeodactylum tricornutum) were strongly inhibited following exposure to raw organic extracts of sediments from Site D5 (Woehang River). The polar fraction separated using a silica gel column significantly inhibited growth rate, esterase activity, cell membrane intensity, and chlorophyll a autofluorescence. In comparison, non- and mid-polar fractions induced non-toxic or esterase inhibition. Target toxicants, such as polycyclic aromatic hydrocarbons, styrene oligomers, and alkylphenols, were detected at low concentrations (450, 79, and 98 ng g−1 dw, respectively) in the sediment of D5, indicating the presence of unmonitored toxicants. FSA was performed for the polar fraction using LC-QTOFMS, and 31 candidates of toxicants were selected. Toxicological confirmation was conducted for 7 candidates for which standards are available. Out of these, 2-nitrophenol, 3-nitrophenol, and 4-nitrophenol showed significant microalgal toxicity; however, these compounds did not fully explain the induced toxicity. Overall, combining EDA and FSA with multiple endpoint bioassays demonstrated the benefits of characterizing the microalgal toxicants in the environments. [ABSTRACT FROM AUTHOR]

Ecotoxicological effects of spilled oils are well documented, but study of recovery of marine benthic communities is limited. Long-term recovery of hard bottom communities during physical and biological remediations after a spill was monitored. A 60-day experiment was conducted using a mesocosm with monitoring of eight endpoints by use of the sediment quality triad (SQT). First, physical treatment of hot water + high pressure flushing maximally removed residual oils (max=93%), showing the greatest recovery among SQT variables (mean=72%). Physical cleanup generally involved adverse effects such as depression of the microphytobenthic community during the initial period. Next, biological treatments, such as fertilizer, emulsifier, enzyme and augmentation of the microbes, all facilitated removal of oil (max=66%) enhancing ecological recovery. Analysis of the microbiome confirmed that oil-degrading bacteria, such as Dietzia sp. and Rosevarius sp. were present. A mixed bioremediation, including fertilizer + multi-enzyme + microbes (FMeM) maximized efficacy of remediation as indicated by SQT parameters (mean=47%). Natural attenuation with "no treatment" showed comparable recovery to other remediations. Considering economic availability, environmental performance, and technical applicability, of currently available techniques, combined treatments of physical removal via hand wiping followed by FMeM could be most effective for recovery of the rocky shore benthic community. [Display omitted] • Mesocosm study first adopting SQT revealed varied oil cleanup efficiencies. • Physical cleanup effectively removed oil, but initially harmed benthic community. • Mixed biological methods increased oil removal efficacy across SQT components. • No treatment" recovered benthic community considerably, highlighting natural attenuation. • Physical hand wiping combined with bioremediation showed the greatest oil recovery. [ABSTRACT FROM AUTHOR]

Abstract: The influence of industrial and/or municipal contaminant inputs on the aquatic environment of Pohang, Korea was investigated, with a focus on bioassay combined with instrumental analysis. Pohang is the most heavily populated city in Gyeongsangbuk-do province of Korea, with more than half a million residents, and also hosts the nation's biggest steel manufacturer and related industries. Sediment (n=15) and surface water samples (n=17) were collected from Hyeongsan River which runs across the Pohang city, in two separate events, i.e., June 2010 and February 2011. Sediment samples were first Soxhlet-extracted (raw extract) and were measured for estrogenicity using H295R cell line, and also analyzed for alkylphenols (APs), bisphenol A (BPA), PAHs, and PCBs. For sediment samples which exhibited greatest effects in the cell line, further fractionation was performed into non-polar, mid-polar, and polar portions. In surface water samples, heavy metals were also analyzed. Among 15 sediment samples, station S2 near the steel industry complex and station M3 near the municipal area showed the greatest sex hormone changes, and these changes were generally explained by the fractions which contained APs and BPA. Principal component analysis (PCA) however suggests that chemicals that were not analyzed in the present study would better explain endocrine disruption capacity of sediments. In water samples, adverse effects on hatchability and growth of Japanese medaka fish, and on Daphnia reproduction were noted following exposure to six water samples collected from stations near industrial and municipal areas. Several heavy metals and nonylphenol (NP) concentrations exceeded surface water quality guidelines, suggesting adverse effects of contamination inputs from both industrial and municipal activities. Observed estrogenicities in stations such as S2 and M3 warrant further investigations on longer term ecosystem impacts near industrial and municipal areas. The levels of major organic chemicals in sediments are quite comparable to those reported in ~10years ago, emphasizing a need for source control. [Copyright &y& Elsevier]