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Recent studies have suggested that rare earth elements (REEs) are contaminants of emerging concern. Moreover, the understanding of the occurrence and risks of REEs in river-estuary-bay systems is limited. The present study investigated the distributions, geochemical characteristics, and ecological risks of Y and 14 REEs (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu) in sediments from the Yellow River to its estuary and adjacent Laizhou Bay. The average total concentrations of Y and REEs in the sediments generally increased from the Yellow River (149 mg/kg) to the estuary (165 mg/kg) and Laizhou Bay (173 mg/kg). In the estuarine core sediments, the concentrations of Y, light REEs (LREEs), and heavy REEs (HREEs) were in the ranges of 19.5–31.4 mg/kg, 58.6–156 mg/kg, and 12.3–19.1 mg/kg, respectively, from the 1700s to 2018, showing no obvious increasing or decreasing trends. The surface and core sediments from the river to the bay were characterized by obvious fractionation between LREEs and HREEs. In sediments, Fe minerals and clay are believed to promote the accumulation of REEs, especially HREEs. The enrichment levels of REEs generally increased from the middle reaches of the Yellow River to the bay, and Gd, Tb, Dy, Ho, Yb, and Lu were the most enriched elements in the sediments. Lu had moderate potential ecological risks in sediments of "the Yellow River−estuary−bay" system, and other REEs had relatively low ecological risks. The potential ecological risk indices of Y and REEs ranged from 78.7 to 144, showing increasing trends from the Yellow River to its estuary and adjacent bay, which should raise concerns regarding emerging contaminant management around estuarine and coastal regions. [Display omitted] • Concentrations of REEs increased from the Yellow River to estuary and Laizhou Bay. • Historical REE contents (1707–2018) of the estuarine sediment core were determined. • Fe minerals and clay promoted the REE accumulation in sediments. • Gd, Tb, Dy, Ho, Yb, and Lu were most enriched elements in the sediments. • Moderate ecological risks of REEs appeared and increased from the river to bay. [ABSTRACT FROM AUTHOR]

To investigate the long-term effects of urbanization and industrialization on coastal trace metal contamination, two sediment cores, Q21 (representing 1965–2018) and Q23 (representing 1986–2018), collected from the adjacent coasts of the east old town and west new area of Qingdao were analyzed. Although the concentrations of As, Cd, Co, Cr, Cu, Ni, Pb, Sc, and Zn were higher in Core Q21, the increasing trends in their concentrations and contamination levels were more obvious in Q23, especially since the 2000s. Moreover, the urbanization rates of the new area (1978–2017) were significantly positively correlated with the historical metal concentrations in Q23. Affected by the rapid socio-economic development in the new area, the combined excessive concentrations of the eight metals (excluding Sc) increased faster in Q23 (0.14–78.4 mg/kg) than Q21 (0.58–45.3 mg/kg). Overall, the sediment Core Q23 experienced higher trace metal contamination and ecological risks than Core Q21. • Historical records of nine metals in two cores of Jiaozhou Bay were investigated. • Excessive concentrations of metals in the sediment cores were quantified. • Rapid urbanization in the western bay accelerated metal enrichment in sediments. • Severe metal contamination could occur in western bay owing to rapid urbanization. [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]

• The impacts of the COVID-19 pandemic on the occurrence of OPEs were investigated. • Total OPE concentrations decreased by 67–70% in waters after the COVID-19 outbreak. • OPEs released from masks were insufficient to increase their concentrations in water. • Spatial distribution of OPEs was affected by riverine inputs & coastal engineering. • TCEP, TNBP, and BDP showed potential ecological risks to aquatic organisms. Organophosphate esters (OPEs) are a group of synthetic chemicals used in numerous consumer products such as plastics and furniture. The Coronavirus Disease 2019 (COVID-19) pandemic significantly slowed anthropogenic activities and reduced the emissions of pollutants. Meanwhile, the mismanagement of large quantities of disposable plastic facemasks intensified the problems of plastic pollution and leachable pollutants in coastal waters. In this study, the joint effects of the COVID-19 outbreak on the occurrence of 12 targeted OPEs in the waters of Laizhou Bay (LZB) were investigated. The results showed that the median total OPE concentrations were 725, 363, and 109 ng L−1 in the sewage treatment plant effluent, river water, and bay water in 2021, decreased significantly (p < 0.05) by 67%, 68%, and 70%, respectively, compared with those before the COVID-19 outbreak. The release potential of targeted OPEs from disposable surgical masks in the LZB area was ∼0.24 kg yr−1, which was insufficient to increase the OPE concentration in the LZB waters. The concentrations of most individual OPEs significantly decreased in LZB waters from 2019 to 2021, except for TBOEP and TNBP. Spatially, a lower concentration of OPEs was found in the Yellow River estuary area in 2021 compared with that before the COVID-19 pandemic due to the high content of suspended particulate matter in the YR. A higher total OPE concentration was observed along the northeastern coast of LZB, mainly owing to the construction of an artificial island since 2020. The ecological risks of the OPE mixture in LZB waters were lower than those before the COVID-19 outbreak. However, TCEP, TNBP, and BDP should receive continuous attention because of their potential ecological risks to aquatic organisms. [Display omitted] [ABSTRACT FROM AUTHOR]

Neonicotinoids (NEOs) and fipronil are widely used in pest control, but their spatiotemporal distribution and risk levels in the "river–estuary–bay" system remain unclear. Between 2018 and 2021, 148 water samples from rivers to inshore and offshore seawater in Laizhou Bay, China were collected to investigate the presence of eight NEOs and fipronil and its metabolites (FIPs). Significant seasonal variations in NEOs were observed under the influence of different cultivation practices and climatic conditions, with higher levels in the summer than in the spring. The average concentrations of total neonicotinoids (ΣNEOs) and ∑FIPs decreased from rivers (63.64 ng/L, 2.41 ng/L) to inshore (22.62 ng/L, 0.14 ng/L) and offshore (4.48 ng/L, 0.10 ng/L) seawater of Laizhou Bay. The average concentrations of ΣNEOs decreased by 85.3 % from 2018 to 2021. The predominant insecticides in the study area were acetamiprid, thiamethoxam, imidacloprid, and fipronil sulfone, with a gradual shift toward low-toxicity and environmentally friendly species over time. Influenced by agricultural intensity, ∑NEOs were mostly distributed in the Yellow River, Xiaoqing River, and their estuaries, where they pose chronic ecological risks. However, FIP exhibited high risk in certain rivers and sewage treatment plants owing to the use of animal repellents or landscape gardening insecticides. This study provides evidence of the transfer of NEOs and FIPs from rivers to the ocean and also clarifies their transition dynamics and changes in risk levels from rivers to oceans. Additionally, the study offers data support for identifying critical pesticide control areas. [Display omitted] • NEOs and FIPs were commonly detected and showed obvious seasonal and regional variation trend. • Acetamiprid, thiamethoxam, imidacloprid, and fipronil sulfone were the dominant insecticides. • Agricultural intensity and anthropogenic emission contribute most to the risk of NEOs and FIPs, respectively. [ABSTRACT FROM AUTHOR]

[Display omitted] Atrazine, a potent herbicide for weeds removal during the growing season, has been widely used in China. It is known to be distributed in aquatic ecosystems with a long half-life, thus presenting a potential risk to species and consumers. This study analyzed the concentrations of degraded atrazine residues in marine organisms (N = 129) including 3 species of mollusks, 2 species of crustaceans, and 15 species of fish from a semi-enclosed bay, Jiaozhou Bay (JZB), adjacent to the Northwest Pacific Ocean in China. The corresponding trophic magnification factors (TMF), bioaccumulation factors (BCFs), and subsequent risks to final consumers were also determined. The results showed an average atrazine concentration of (0.301 ± 0.03) ng g−1 and (0.305 ± 0.04) ng g−1 in fish and invertebrates, respectively. The BCFs were (5.23 ± 1.75) L kg−1 and (5.81 ± 1.31) L kg−1 for fish and invertebrates, respectively. Atrazine was significantly bio-diluted in JZB through the sampled marine organisms with increasing trophic levels, with a TMF value below 1 (P < 0.01). An analysis of the species sensitivity distribution (SSD) predicted that<0.02% of species were exposed to a dissolved concentration of atrazine (57.88 ng L−1) that would lead to detrimental effects, while risk quotients predicted low long-term risks for species in the bay. Finally, people with a diet limited to species from JZB were found to face no associated health risk due to a significantly small daily intake and target hazard quotient of atrazine. The corresponding non-carcinogenic effect showed no significant risk from seafood consumption. [ABSTRACT FROM AUTHOR]

• The urbanized bay was heavily contaminated by amoxicillin and fluoroquinolones. • Total antibiotic concentrations were 71.8~840 ng L −1 for the estuarine water and 38.7~181 ng L −1 for the bay water. • Total antibiotic concentrations in the bay water were significantly higher in winter than in summer. • Spatiotemporal changes in antibiotics were driven by their sources and runoff dilution. • Amoxicillin and enrofloxacin presented high risks to algae in the urbanized bay. The occurrence, temporal variation, and spatial variation of antibiotics in coastal bays and estuaries worldwide are not well documented or understood. Fifteen target antibiotics within the five classes of β-lactams, amphenicols, macrolides, fluoroquinolones, and sulfonamides were measured during the summer and winter in the water of Jiaozhou Bay in China, which is a semi-enclosed urbanized bay. Fourteen antibiotics (excluding tylosin) were detected, thus demonstrating the widespread occurrence of their residues in the bay. The total antibiotic concentration ranged from 71.8 ng L −1 to 840 ng L −1 for the estuarine water, which was significantly higher than that for the bay water (38.7–181 ng L −1). The antibiotic classes in the bay water were dominated by fluoroquinolones and β-lactams, which accounted for nearly 90% of the total antibiotic concentration. In addition, amoxicillin contamination was the most prominent among the 14 detected antibiotics as it accounted for ~44% of the total antibiotic concentration. The concentrations of amoxicillin, leucomycin, enrofloxacin, and sulfamonomethoxine in the bay water were usually higher than those reported for coastal bays and estuaries worldwide. The average total antibiotic concentration in the bay water was 84.7 ng L −1 during the summer, which was significantly lower than that during the winter (129.0 ng L −1). This was mainly due to high dilution by runoff during the summer. The florfenicol concentration in the bay water was significantly higher during the summer than in winter due to its higher usage in aquaculture during the summer. Spatially, the total antibiotic concentration (both summer and winter) was higher in the water along the eastern coast of the bay, where the population and hospital densities are high. However, the sum of the veterinary antibiotic concentrations was higher in the northeastern aquaculture area of the bay during the summer. A risk assessment revealed that amoxicillin and enrofloxacin could pose high risks (risk quotient of > 1) to algae in the bay. The synergic effects of pharmaceutical mixtures and the bioaccumulation of antibiotics through the food web should be considered in future studies. Image, graphical abstract [ABSTRACT FROM AUTHOR]