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Abstract: Spatial distribution of nonylphenol polyethoxylates (NPEOs) and nonylphenol (NP) was investigated in a field study in Lanzhou Reach of the Yellow River. NPEOs and their metabolites were found in the river, with the maximum dissolved concentrations of 6.38 nmol/L for NPEOs, 0.19 nmol/L for nonylphenol ethoxy acetic acids (NPECs) and 0.79 nmol/L for NP, respectively. The maximum concentrations in the sediment and suspended particle samples were 1.50 and 5.09 nmol/g for NPEOs and NP, respectively. The effects of particles, light and microorganism on the dissipation of NPEOs in the river water were investigated based on lab-scale experiments. When natural particles were removed, 72% and 22% degradation of NPEOs were achieved at 120 h in non-sterile and sterile conditions with light, respectively. Different concentrations of NPECs were also observed in these experiments. When suspended particle matters (SPMs) were present, about 38–50% of NPEOs were sorbed to the particulate phase in only 1 h. As a result, the degradation of NPEOs and production of NPECs were inhibited. However, the combined sorption and degradation in the presence of SPMs resulted in lower dissolved NPEO concentrations than those in the absence of SPMs. Biodegradation was the most important pathway for NPEOs degradation in the river water, while NPECs seemed to be produced through both biological and abiological pathways. [Copyright &y& Elsevier]

[Display omitted] • Nanoplastics result in significant hepatic immune toxicity in zebrafish larvae. • Nanoplastic accumulation contributes to the ROS generation and the immunotoxicity. • Nanoplastics activate steroid hormone biosynthesis. • Immune transgenic zebrafish is sensitive to the immunotoxicity of nanoplastics. Nanoplastics in aquatic environments may induce adverse immunotoxicity effects in fish. However, there is insufficient evidence on the visible immunotoxicity endpoints in the larval stages of fish. The liver plays an important role in systemic and local innate immunity in the fish. In this study, the hepatic inflammatory effects of polystyrene (PS) nanoplastic particles (NPs: 100 and 50 nm) and micron PS particles on transgenic zebrafish (Danio rerio) larvae were estimated using fluorescent-labeled neutrophils, macrophages, and liver-type inflammatory binding protein (fabp10a). Particles with smaller size induced higher aggregations of neutrophils and apoptosis of macrophages in the abdomen of the larvae, corresponding to greater hepatic inflammation in the larvae. NPs increased the expression of fabp10a in the larval livers in a dose- and size-dependent manner. PS particles of 50 nm at a concentration of 0.1 mg·L−1 increased the expression of fabp10a in the larval liver by 21.90% (P < 0.05). The plausible mechanisms of these effects depend on their distribution and the generation of reactive oxygen species in the larvae. Metabonomic analysis revealed that the metabolic pathways of catabolic processes, amino acids, and purines were highly promoted by NPs, compared to micron PS particles. NPs also activate steroid hormone biosynthesis in zebrafish larvae, which may lead to the occurrence of immune-related diseases. For the first time, the liver was identified as the target organ for the immunotoxicity effects of NPs in the larval stage of fish. [ABSTRACT FROM AUTHOR]