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In this study, surface seawater, bottom seawater and surface sediments were collected from the Yellow River Estuary Area (YREA) and the Laizhou Bay (LB) to investigate the occurrence, spatial distribution and geochemical control factors for total mercury (THg) and methylmercury (MeHg) in different phases. The geochemical characteristics of seawater and sediments suggested significant variances in the YREA and the LB. The high contamination of Hg in the YREA showed the discharge of the Yellow River (YR) contributed significantly to the Hg contamination in the LB. The partial least squares regression (PLSR) model was utilized to explore the complicated interactions between geochemical controls and methylation potentials in different phases. Although the ecological risk (ER) of Hg was not significant in this study area, the higher values of ER in the YREA suggested that the YR was the primary Hg contributor to LB. Therefore, the potential Hg risk should not be ignored. [Display omitted] • Yellow River discharge greatly contributed to Hg contamination in the Laizhou Bay. • The partial least squares regression model explored MeHg geochemical controls. • MeHg in sediments was more predictable than DMeHg and PMeHg in seawater. • The higher Hg risk was observed in the Yellow River Estuary Area. [ABSTRACT FROM AUTHOR]

The concentrations, sources, and ecological risks of nine trace elements in nine rivers flowing into Laizhou Bay were investigated. The dissolved element concentrations were 1.85–74.4, 0.01–0.47, 0.15–3.46, 1.54–19.7, 2.92–45.1, 1.72–11.5, 1.02–8.35, 0.10–1.02, and 21.4–185 μg/L for As, Cd, Co, Cr, Cu, Ni, Sc, Pb, and Zn, respectively. Zinc was the most abundant element in the sediments, with an average concentration of 106 mg/kg, followed by Cr (64.5 mg/kg), Cu (25.5 mg/kg), Pb (24.3 mg/kg), Ni (23.4 mg/kg), Co (10.9 mg/kg), Sc (8.14 mg/kg), As (6.75 mg/kg), and Cd (0.16 mg/kg). Elements including Co, Cr, Ni, and Sc were mainly from natural sources and As, Cd, Cu, Pb, and Zn were largely influenced by anthropogenic activities such as agricultural practice, industrial production, river transportation, and urbanization. Overall, the rivers flowing into Laizhou Bay experienced slight pollution and ecological risk. However, the severe element contamination in Jie River deserves continuous attention. • Zn was the most abundant element in the water and sediments of coastal rivers. • Co, Cr, Ni, and Sc were mainly from lithogenic sources in these coastal rivers. • As, Cd, Cu, Pb, and Zn were largely influenced by anthropogenic activities. • Severe trace element contamination in the Jie River deserves continuous attention. [ABSTRACT FROM AUTHOR]

The occurrence, spatiotemporal variations, influence factors and environmental risks of eight common neonicotinoids (NEOs), fipronil, and three fipronil metabolites (fipronil and its metabolites are collectively referred to as FIPs) in different seasons from the estuary to the inner area of Jiaozhou Bay, China were comprehensively investigated. First- and second-generation NEOs were found to be the predominant pesticides in this area. The average contents of ∑NEOs and ∑FIPs from the estuary to the inner bay decreased from 12.99 ng/L to 0.82 ng/L and from 1.10 ng/L to 0.17 ng/L, respectively. NEO and FIP concentrations were higher in summer and autumn. High ∑NEO content is distributed in main inflow rivers, such as Dagu River and Licun River, which are influenced by pesticide application. NEO concentrations in all rivers were high upstream and low downstream because of the influence of heavy rainfall and seawater dilution in summer. NEO concentrations were high along the coast and low at the mouth and center of Jiaozhou Bay in summer and autumn and evenly distributed in winter and spring. Temperature has a great influence on most NEOs and FIPs owing to its effect on their degradation. Nitrogen-containing nutrients have an important influence on the distribution of fipronil and acetamiprid, which may be due to the activity of nitrogen-containing functional groups in their structure. Only Licun River, Dagu River and Haibo river sewage treatment plant in summer posed a certain risk of chronic toxicity for NEOs using the new threshold established by the species sensitive distribution (SSD) method for Chinese native aquatic lives. These findings should arouse people's attention. [ABSTRACT FROM AUTHOR]

In this study, water and sediment samples from the Jiaozhou Bay and surrounding rivers were collected to analyze the seasonal occurrence and allocation of 12 organophosphate esters (OPEs) and the associated ecological risk. The higher contamination of OPEs in the adjacent rivers indicated the impact of terrestrial input. Tris(1-chloropropan-2-yl) phosphate (TCIPP) was the predominant OPE in the four environmental sample groups investigated. The spatial distribution of OPEs in seawater varied greatly seasonally and was mainly affected by terrestrial input, with OPEs being redistributed under the influence of tidal currents. The partition coefficients (log K oc) of the OPEs were calculated, and their strong correlation with the log K ow (octanol-water) values suggested that the water-sediment allocation was significantly affected by hydrophobicity. The homologous relationships among the 7 OPEs with detection frequencies greater than 40% were identified by principal component analysis (PCA). The partial least squares regression (PLSR) model explicated that ∑OPEs cycling dynamics and principal controlling factors were dissimilar in the bay versus surrounding rivers. The risk quotient (RQ) faced by typical organisms in seawater and river water indicated that short-term OPEs exposure was safe for green algae, daphnia and fish. The organisms in rivers faced the higher ecological risk of OPEs in spring than in summer and winter. Therefore, the terrestrial transport of OPEs in spring should be controlled. [Display omitted] • The spatial distribution of OPEs in seawater showed seasonal variations. • The calculated log K oc of OPEs displayed significant correlation with log K ow. • The partial least squares regression explored ∑OPEs cycling dynamics. • Risk of OPEs was higher in rivers than in the bay for green algae, daphnia and fish. The partial least squares regression (PLSR) model indicated dissimilar source dynamics and principal controlling factors in the bay versus surrounding rivers. [ABSTRACT FROM AUTHOR]

Endocrine-disrupting chemicals (EDCs) in water are receiving particular attention as they pose adverse effects on aquatic systems, even at trace concentrations. A comprehensive study was conducted on 14 EDCs (five estrogens and nine household and personal care products (HPCPs)) in the water of the urbanized Jiaozhou Bay in the Yellow Sea during summer and winter. Results showed that the total concentration of 14 EDCs ranged from 100 to 658 ng L−1 and 56.7–212 ng L−1 in the estuarine and bay water, respectively. The average total concentration of five estrogens in summer was significantly (p < 0.05) lower than that in winter due to the higher precipitation dilution and degradations during summer, whereas the average total concentration of nine HPCPs was significantly (p < 0.05) higher during the summer than that during the winter because of the higher usage and emissions during the summer. Estrogens and HPCPs were dominated by 17α-ethinylestradiol and p-hydroxybenzoic acid (PHBA), respectively. High PHBA concentrations may be related to the hydrolysis of parabens. The total concentrations of EDCs were higher in the eastern coastal seawater of the bay due to the strong influence of domestic and industrial wastewater discharge. Estrogens may interfere with the endocrine system of aquatic organisms in the bay because the total estradiol equivalent concentration exceeded 1 ng L−1. 17α-ethinylestradiol was the main contributor to the estrogenic activity. The EDC mixtures posed high risks (RQ > 1) to mollusks, crustaceans, and fish, and low to moderate risks (RQ < 1) to algae. Fish was the most sensitive aquatic taxon to the EDC mixtures. Given the concentration and frequency of EDCs, the optimized risk quotient method revealed that 17α-ethinylestradiol, estrone, triclocarban, triclosan, and 17β-estradiol should be prioritized in ecological management because of their high risks (prioritization index of >1). [Display omitted] • Endocrine-disrupting chemicals (EDCs) are widely detected in an urbanized bay. • Estrogen concentration is lower in summer due to high rainfall and degradation. • Household and personal care products (HPCPs) was high in summer due to high use. • Impacted by riverine input, EDC concentration was high in the eastern bay coast. • Five priority EDCs with high ecological risks were identified. [ABSTRACT FROM AUTHOR]

The ubiquitous and adverse effects of estrogens have aroused global concerns. Natural and synthetic estrogens in 255 water samples from the southern Bohai Sea were analyzed over three years. Total estrogen concentrations were 11.0–268 ng/L in river water and 1.98–99.7 ng/L in seawater, with bisphenol A (BPA) and 17α-ethynylestradiol (EE2) being the predominant estrogens, respectively. Estrogen showed the highest concentrations in summer 2018, followed by spring 2021 and spring 2019, which was consistent with the higher estrogen flux from rivers during summer. Higher estrogen concentrations in 2021 than in 2019 were driven by the higher level of BPA, an additive used in personal protective equipment. Estrogen exhibited higher concentrations in the southern coast of the Yellow River Delta and the northeastern coast of Laizhou bay due to the riverine input and aquaculture. Estrogens could disturb the normal endocrine activities of organisms and edict high ecological risks (90th simulated RQ T > 1.0) to aquatic organisms, especially to fish. EE2 was the main contributor of estrogenic potency and ecological risk, which requires special concern. This is the first comprehensive study of estrogen spatiotemporal variations and risks in the Bohai Sea, providing insights into the environmental behavior of estrogens in coastal regions. [Display omitted] • BPA and EE2 were dominant in river water and seawater, respectively. • Riverine input & mariculture lead to higher estrogen levels in summer than spring. • Spatial distribution of estrogens was influenced by mariculture and riverine input. • Estrogens caused high risks to aquatic organisms, particularly to fish. • EE2 was the main contributor of estrogenic potency and ecological risk. [ABSTRACT FROM AUTHOR]

Fourteen perfluoroalkyl substances (PFASs) in fishery organism, surface seawater, river water, rainwater, and wastewater samples collected from Jiaozhou Bay (JZB) in China and its surrounding area were determined to understand their contamination status, sources, health risk, and causes of spatiotemporal variations in the aquatic environment of a temperate bay adjacent to a metropolis. The total concentration of PFASs in 14 species of fishery organisms ranged from 1.77 ng/g to 31.09 ng/g wet weight, and perfluorooctane sulfonate (PFOS) was the dominant PFAS. ∑PFASs concentration in surface seawater ranged from 5.54 ng/L to 48.27 ng/L over four seasons, and dry season (winter and spring) had higher levels than wet season (summer and autumn). Perfluorooctanoic acid (PFOA) was the predominant individual PFAS in seawater, indicating that notorious C8 homologs remained the major PFASs in this region. The seasonal variation in seawater concentrations of three major PFASs, namely, PFOA, perfluoroheptanoic acid, and perfluorononanoic acid, was similar to that of ∑PFASs. However, the seasonal variation of PFOS concentration was different from that of ∑PFASs, with the lowest in winter and the highest in spring. In general, seasonal variations of terrigenous input and water exchange capacity were the main reasons for the spatiotemporal variation of PFASs in the aquatic environment of JZB. Moreover, bioselective enrichment for individual PFAS affected the partition of PFASs in different environment medium. Wet precipitation, sewage discharge, and surface runoff were the main sources of PFASs in this area. Nevertheless, the contribution of different sources to individual PFAS indicated a clear difference, and wastewater and river water were not consistently the most important source for every PFAS. Preliminary risk assessment revealed that the consumption of seafood, especially fish, from JZB might pose a certain extent of health risk to local consumers based on their estimated daily intake of PFASs. Image 1 • Various PFASs occurred in the fishery organisms and aquatic environment of Jiaozhou Bay. • Notorious C8 homologs (PFOA and PFOS) were still the dominant PFASs. • The levels of PFASs in seawater evidently varied with the season and location. • Terrigenous input, tide, and rainfall affected the spatiotemporal variation of PFASs. • Health risks for PFAS exposure via fishery organism intake cannot be ignored. [ABSTRACT FROM AUTHOR]

Paralytic shellfish toxins (PSTs) producing algae are widely distributed in the global coastal aquatic environment, posing a threat to coastal ecosystem health and mariculture safety. However, the levels and potential environmental risks of PSTs frequently detected in shellfish remain largely unexplored in seawater of mariculture zones. In this study, a new method for trace detection of 13 common PSTs (<1.0 ng/L) in seawater was established based on off-line solid phase extraction (SPE) and on-line SPE-liquid chromatography-tandem mass spectrometry (on-line SPE-LC-MS/MS), and a systematic investigation of PSTs in seawater of the Laizhou Bay, a typical aquaculture bay in China, was conducted to understand their pollution status, environmental impact factors and ecological risks for the first time. Eleven PSTs were detected in the seawater of Laizhou Bay with total concentrations ranging from 0.75 to 349.47 ng/L (mean, 176.27 ng/L), which indicates the rich diversity of PSTs in the mariculture bay and demonstrates the reliability of the proposed analytical method. C1, C2, GTX2, GTX3, dc GTX2, and dc GTX3 were found to be the predominant PSTs, which refreshed the knowledge of PST contamination in the coastal aquatic environment. PST levels in seawater exhibited the highest levels in the southeastern mouth of Laizhou Bay and decreased toward the inner bay. Correlation analyses showed that climatic factors, nutrient status and hydrological conditions had significant effects on the distribution of PST in mariculture bay. Preliminary environmental risk assessments revealed that aquatic organisms throughout the waters of Laizhou Bay are at risk of chronic PST toxicity. These findings imply that the risk of PST in seawater of mariculture bay has previously been grossly underestimated, and that the coastal aquatic environment in North China and even the world may be at more serious risk of PST pollution, which should be taken seriously. [Display omitted] • A new analytical method was developed for 13 trace PSTs in seawater (<1.0 ng/L). • Various PSTs widely distributed in nearshore water was reported for the fist time. • GTXs, dc GTXs, and C-toxins are the predominant PSTs in mariculture seawater. • Aquatic organisms in the Laizhou Bay are generally at risk of chronic PST toxicity. • Nutrient and hydrological conditions affect the distribution of PST in Laizhou Bay. [ABSTRACT FROM AUTHOR]

Heavy metal (HM) pollution in coastal ecosystems have posed threats to organisms and human worldwide. This study comprehensively investigated the concentrations, sources, trophodynamics, contamination, and risks of six HMs in the coastal ecosystem of Jiaozhou Bay, northern China, by stable isotope analysis, positive matrix factorization (PMF), and Monte Carlo simulation. Overall, Co, Cu, Ni, Pb, and Zn were significantly bio-diluted in the food web, while Cr was significantly biomagnified with a trophic magnification factor of 1.23. In addition, trophodynamics of the six HMs was different among fish, mollusk, and crustacean. Furthermore, detailed transfer pathways of six HMs in the food web including eight trophic levels were different from one another. Bioaccumulation order of the six HMs was Cu > Zn > Co, Cr, Ni, and Pb. Zinc concentrations were the highest in seawater, sediments, and organisms. Anthropogenic sources contributed to 71% for Zn, 31% for Cu and Pb, and 27% for Co, Cr, and Ni in the sediment, which was moderately contaminated with moderate ecological risk. However, the human health risk of HMs from eating seafood was relatively low. To protect the Jiaozhou Bay ecosystem, HM contamination should be further controlled in future. [Display omitted] • Biodilution/biomagnification of six metals in the Jiaozhou Bay were quantified. • Quantitative trophic transfer pathways of six metals in the bay were identified. • Bioconcentration factors of six metal for eight trophic levels were calculated. • Trophodynamics of six metals was different among fish, mollusk, and crustacean. • Ecological and health risks of six metals in the bay were assessed. [ABSTRACT FROM AUTHOR]

We investigated the spatiotemporal distributions, risks, and prioritization of 15 widely used antibiotics in Laizhou Bay (LZB). Water samples (145) were collected from LZB and its estuaries and analyzed. Twelve antibiotics, with total concentrations of 241–1450 and 69–289 ng L−1 in estuarine water and seawater, respectively, were detected, with the contributions of norfloxacin, ciprofloxacin, and amoxicillin exceeding 70%. Amoxicillin was firstly determined, which contributed to 20% and 46% of the total antibiotics during summer and spring, respectively. Higher antibiotic concentrations were observed in the sea located adjacent to aquaculture bases and the Yellow River Estuary, which are significantly influenced by mariculture and riverine inputs, respectively. Veterinary antibiotics showed higher total concentrations in summer compared to spring, indicating a higher degree of their usage in mariculture in summer. The antibiotic mixtures posed high risk to algae and low to medium risks to crustaceans and fish. Amoxicillin and norfloxacin were identified as high-risk pollutants. Additionally, amoxicillin and ciprofloxacin showed medium to high resistance development risks. Previous studies on antibiotics in the LZB did not determined amoxicillin and thus underestimated antibiotic contamination, ecological risk, and resistance development risk. Amoxicillin, norfloxacin, and ciprofloxacin should be prioritized in risk management. [Display omitted] • Amoxicillin in the Laizhou Bay water was firstly determined. • Norfloxacin and amoxicillin concentrations were higher than other compounds. • Mariculture & Yellow River inputs affected antibiotic spatiotemporal distribution. • Veterinary antibiotics showed higher concentrations in summer than in spring. • Priority antibiotics with high ecological and/or resistance risks were identified. [ABSTRACT FROM AUTHOR]

• Increasing trend in vanadium concentrations in aquatic organisms from Asia. • Increases in vanadium concentrations comparable to those from vanadium production. • HC5 for seawater species estimated to be 1.13 (0.05–21.19) μg|L-1. • High and moderate risks to aquatic organisms from seawater concentrations. • Moderate and low health risks from seafood consumption to the 95th percentile group. Vanadium has been classified as a potentially toxic metal and has been given limited attention in comparison to similar trace metals. Similarly, worldwide and continental vanadium pollution and risks remain contested. Here, we synthesized the worldwide concentration of vanadium in marine ecosystems with the relevant ecological and human health risks. We found that vanadium in biota and seawater collected from Asia shows significant increases over the temporal analysis, with rates similar to those reported for vanadium consumption and production. Furthermore, invertebrates have a higher concentration of vanadium than fishes. Similarly, we demonstrate that sediments classified as polluted have concentrations that are not directly correlated with the highest concentrations across continents. Finally, ecological risks were higher from seawater, with potential impacts to 55% of aquatic species in Asia estimated from chronic species sensitivity distribution (SSD). The concentration endangering only 5% of seawater species (HC5) was estimated as 1.13 (0.05–21.19) μg L-1. Estimated daily intakes revealed that overall, there are none to low health risks from aquatic product consumption, yet high risks are plausible to children with consumption patterns in the 95th percentile. [Display omitted] [ABSTRACT FROM AUTHOR]

In this study, 26 surface seawater samples, 26 surface sediment samples and 114 organisms were collected to study the trophic transfer and dietary exposure risk of mercury (Hg) in organisms from the Jiaozhou Bay, which is a typical semi-enclosed urbanized bay. The total mercury (THg) and methylmercury (MeHg) concentrations did not exceed the threshold limits and performed as: fish > crustaceans > mollusks. The trophic level values (TLs) were less than 3 in all the groups, indicating simple structure of food chain. With the increasing δ15N value, THg and MeHg were significantly biomagnified in the mollusks and fish but not in the crustaceans. In addition, the bioaccumulation and biomagnification of MeHg were higher than inorganic mercury (IHg) in the aquatic food chain. Target hazard quotient (THQ) and provisional tolerable weekly intake (PTWI) indicated that Hg exposure via consumption of seafood from the Jiaozhou Bay did not pose significant health risks for general population. Consuming fish will face the higher health risk than crustaceans and mollusks, especially in urban regions. Moreover, the risk of MeHg caused by intaking seafood deserved more attention. Trophic transfer function (TTF) explicated the transfer of Hg in the ecosystem and higher trophic transfer efficiency of MeHg than IHg. TTF interpreted the terrestrial input of Hg should be controlled to ensure the safety of consuming seafood from the Jiaozhou Bay. [Display omitted] • Hg concentrations in aquatic samples did not exceed the threshold limit. • Hg biomagnification was observed in marine organisms in the Jiaozhou Bay. • Trophic transfer of MeHg was more obvious than IHg. • Health risk of consuming seafood was more significant in urban regions. • The terrestrial input of Hg should be controlled. [ABSTRACT FROM AUTHOR]