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[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]

In several watersheds, agricultural activities are the cause of pollution, mainly due to the discharge of herbicides. Often, these herbicide plumes are transported to the surrounding bays. Samples of water, suspended particulate sediments (SPSs), and sediments from 37 sites in the Jiaozhou Bay in the western Pacific Ocean were collected in April 2018. The total concentrations of atrazine and acetochlor in these samples were analyzed, that showed different patterns in each sampled area. Atrazine had 2–3 times higher concentrations in coastal areas and bays compared to the estuary, indicating that it had a higher residence time in the marine environment. In contrast, acetochlor concentration decreased with an increase in the depth of seawater. Both the spatial distributions and the vertical concentrations in water, SPS, and sediment proved that these two herbicides had different responses during transportation from the estuary to the bay. Despite the significant difference in concentration of the two herbicides in the water and sediment, their spatially averaged value in SPS was very close, indicating that the particles had saturated sorption capability. The organic carbon normalized partition coefficient (LogK oc) was used to explain the partitioning of the herbicides between water and sediment. The LogK oc difference between herbicides demonstrated that acetochlor was strongly phase partitioned in the coastal and the bay areas, thereby causing similar distributions of acetochlor in the three matrices. Atrazine had a higher LogK oc value in the estuary, which explained its higher concentration in the estuary SPS. The correlation and redundancy analyses both demonstrated that the concentrations of the herbicides in water were sensitive to dissolved organic carbon and dissolved oxygen. The current tides and bathymetry were the critical factors in determining the spatial distribution of herbicides in the water and sediment, resulting in a low herbicide load in the river mouth area. • Atrazine had higher concentrations in seawater and suspended sediment from estuary to bay. • Acetochlor has lower value in seawater and suspended sediment in the bay. • Organic carbon normalized partition coefficient proved acetochlor has strong partition process in bay. • Spatial patterns of two kinds of herbicides in the bay demonstrated their source and distribution. [ABSTRACT FROM AUTHOR]