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Excessive accumulation of Zn2+ or Ni2+ can cause various problems to aquatic animals. In this study, the developmental toxicity induced by individual or combined exposure of Zn2+ and Ni2+ to zebrafish embryos and larvae were evaluated to better understand the interaction between Zn2+ and Ni2+ . Both of individual and combined exposure of Zn2+ and Ni2+ could cause obvious developmental toxicity, which mainly occurred after hatching, at a concentration-dependent manner. The calculated 168-h LC50 were 2.79 mg/L for Zn2+ and 7.44 mg/L for Ni2+ . The interaction of Zn2+ and Ni2+ based on mortality was found to be an antagonism. Various malformations, including tail curving, spinal curvature, pericardial edema, and yolk sac edema, were observed with significant effects on body length and heartbeat rates after exposure of Zn2+ and Ni2+ . Meanwhile, some genes related to cardiovascular development and bone formation were mainly down-regulated by the individual and combined exposure of Zn2+ and Ni2+ . The individual exposure was more toxic than combined exposure because the interaction of Zn2+ and Ni2+ was determined to be an antagonism. The down-regulation of genes related to cardiovascular development and bone formation may contribute to the observed malformation and decreases of body length and heartbeat rates.

The distribution character of 41 antibiotics belonging to 6 groups, sulfonamides (SAs), quinolones (QUs), tetracyclines (TCs), macrolides (MLs), penicillins (PLs), and chloramphenicol (CHL), was investigated in drinking water sources of Nanjing during 2017–2019. MLs (42.98%) were the most abundant category, followed by SAs (25.94%) and QUs (22.52%). The dominant antibiotic was ofloxacin (OFX) in Dec. 2017 (average concentration, 3.14 ng/L; range, ND–35.20 ng/L) and Nov. 2018 (2.16 ng/L, ND–12.26 ng/L), and sulfadiazine (SDZ) in Mar. 2019 (16.37 ng/L, ND–25.90 ng/L). For Dec. 2017, the total concentrations in Zhongshan Waterworks (S15) and Jinniushan Reservoir (S16) were significantly higher than the other sampling sites, which may be attributed to point source pollution. The ecological and human risk of the main antibiotics was assessed by risk quotients (RQs) and target hazard quotient (THQ), respectively. Most of the RQ values were below 0.1, except enrofloxacin (ERX, 0.11) and enoxacin (ENX, 0.62) in Dec. 2017, lomefloxacin (LOM, 0.14) in Nov. 2018, and LOM (0.28) and ERX (0.10) in Mar. 2019. This indicated that the risk of the target antibiotics to aquatic organisms in the 3 years was moderate or low level. Meanwhile, results of the THQ values showed that antibiotic exposure caused no risk to human health. This research provides scientific information for antibiotic pollution control and enriches environmental monitoring data in the drinking water sources.

In this work, Caenorhabditis elegans was employed as an in vivo model to determine the toxic effects of atrazine at different concentrations. After the exposure period from the larval stage L1 to adulthood day 1, atrazine (10 mg/L) significantly decreased the body length and lifespan of nematodes. In addition, exposure to ≥0.01 mg/L atrazine remarkably increased the intestinal reactive oxygen species (ROS) levels and reduced locomotion behavior of nematodes, while exposure to ≥ 1 mg/L atrazine decreased the brood size of nematodes. Moreover, atrazine (0.001–0.1 mg/L) upregulated the expression levels of hsp-6::GFP and hsp-6/60 in nematodes, indicating the activation of mitochondrial unfolded protein response (mtUPR). On the contrary, atrazine (1–10 mg/L) downregulated the expression levels of hsp-6::GFP and hsp-6/60 in nematodes. Furthermore, mtUPR induction governed by the RNAi knockdown of atfs-1 could increase the vulnerability of nematodes against atrazine toxicity. Overall, our findings highlighted the dynamic responses of nematodes toward different concentrations of atrazine, which could be monitored using different sublethal endpoints as bioindicators.