Table 2.
Exposure Duration | Age at Exposure | Species | Chemical | LOEC1(ppb2) | Major Endpoints | Reference |
---|---|---|---|---|---|---|
4d | Adult | Fathead minnows | Cd3 | 2.5 | Increase in auditory threshold | Low and Higgs (2015) |
1d | 2–5 dpf | Rainbow trout | Cd3 | 2 | Higher growth rate, altered social behavior & olfactory accumulation | Sloman et al. (2003) |
4h/day for 8d | Juveniles | Sea bass | Cd3 | 0.5 | Sensory macula damage and impaired escape behavior | Faucher et al. (2008) |
4h | Juveniles | Sea bass | Cd3 | 5 | Neuromast damage | Faucher et al. (2006) |
21d | Adults (Males) | Zebrafish | Cd3 | 1.9 | Increased apoptotic (c-jun) & detoxifying genes (mt1 & mt2) at 21d | Gonzalez et al. (2006) |
1d | Adults | Zebrafish | Cd3 | 110 | Induction of nrf2 antioxidant genes (increased olfactory neuron cell death) | Wang and Gallagher (2013) |
30d | Adults | Zebrafish | Cd chloride(CdCl2) | 183 | Changes in retinal morphology & ultrastructure, increased light sensitivity | Avallone et al. (2015) |
1 – 6h | Adults | Zebrafish | Cd3 | 200 | Increased mt2 and smtb | Wu et al. (2016) |
2d, 7d, 16d | Adults | Zebrafish | CdCl2 | 613 | Decrease in glial fibrillary acidic protein | Monaco et al. (2016) |
1d, 4d | Adult (Females) | Zebrafish | Cd3 | 1000 | Increased ROS, nitric oxide, & malondialdehyde in brain and liver | Zheng et al. (2016) |
3d | Adult (Females) | Zebrafish | Cd3 | 1000 | Induction of mt2, smtb, and accumulation of Cd in ovaries and F1 larvae at 72hpf | Wu et al. (2012) |
2d | Adults | Zebrafish | CdCl2 | 26122 | LC50 and AChE inhibition | Zhang et al. (2017) |
10m | Adult Brain | Zebrafish | Cd acetate Cd(CH3COO)2 | 28102 | Nucleotide hydrolysis | Senger et al. (2006) |
2d | 3–5 dpf | Zebrafish | CdCl2 | 9 | Increased mt2 and smtb | Wu et al. (2008) |
4d | 3–7 dpf | Zebrafish | Cd3 | 112 | Cell death, altered histological and changes in olfactory dependent behavior. | Matz and Krone (2007) |
3h | 80 – 83 hpf | Zebrafish | Cd3 | 562 | Reduced olfactory dependent predator response | Blechinger et al. (2007) |
12h | Juvenile | Zebrafish | Cd3 | 970 | Increased ROS and immunotoxicity | Zheng et al. (2017) |
50d | 0–50 dpf | Zebrafish | Cd3 | 20 | Lower survival at 24 hpf and reduced olfactory-dependent predator response (64 dpf) | Kusch et al. (2008) |
3d | 0–72 hpf | Zebrafish | CdCl2 | 112 | cyp19a1b gene expression and anti-estrogenic activity | Chouchene et al. (2016) |
3d | 0–72 hpf | Zebrafish | CdCl2 | 112 | Altered adult hyperactivity and antioxidant physiology | Ruiter et al. (2016) |
4d | 0–96 hpf | Zebrafish | Cd3 | 112 | Behavioral alteration, oxidative stress, immunotoxicity | Jin et al. (2015) |
5d | 0–120 hpf | Zebrafish | CdCl2 | 560 | Induction of mt in olfactory pits and neuromast | Chen et al. (2007) |
4d | 0–96 hpf | Zebrafish | Cd3 | 2000 | Reduction in neural crest gene expression and hypopigmentation | Zhang et al. (2015) |
3d | 0–72 hpf | Zebrafish | Cd3 | 2040 | Neuromast damage | Sonnack et al. (2015) |
~1d | 4–24 hpf | Zebrafish | CdCl2 | 6893 | Hyperpigmentation, reduced retinal ganglion projections, no photoreceptors, reduced neuronal projections | Hen Chow et al. (2009) |
~1d | 4–24 hpf | Zebrafish | CdCl2 | 11241 | Decreased head size, unclear brain divisions, reduced proneuronal gene expression | Chow et al. (2008) |
Lowest Observed Effect Concentration;
parts per billion;
Species not specified.