FIGURE SUMMARY
Title

Behavioural response to toxic elements, detoxification and organ accumulation are time-of-day-dependent in zebrafish

Authors
Guidi, C., Martínez-López, E., Oliver, J.A., Sánchez-Vázquez, F.J., Vera, L.M.
Source
Full text @ Chemosphere

Fig. 1. Schematic diagram of the experimental design.

Fig. 2. Swimming activity of control (top), Hg- (middle) and As-exposed (bottom) zebrafish at ML (left panels) and MD (right panels) (n = 14 fish/trial). Activity levels were normalized as the percentage of maximum velocity displayed by fish during each trial. As and Hg exposure period are indicated by a grey rectangle.

Fig. 3. Mean locomotor activity level (cm/s) of control (top), Hg- (middle) and As-exposed (bottom) zebrafish at ML (left panels) and MD (right panels) (n = 14 fish/trial). Each bar indicates the average activity level during 30 min ±SE. White and black bars represent activity data from non-exposed fish (control) and before adding the metals to the aquarium at ML and MD, respectively. Pattern filled bars represent data from Hg- (dots) and As-exposed (grid) fish. Asterisks (*) indicate statistically significant differences in mean activity levels between the first and the subsequent 30-min slots (GLM Repeated measures followed by pairwise comparisons, Bonferroni adjusted, p < 0.05).

Fig. 4. Relative expression of antioxidant genes in gills (left panels) and liver (right panels) of control and Hg-exposed zebrafish at ML (white bars) and MD (black bars): sod1, gpx7, gsr and cata. Data are shown as the mean ± SE (n = 7). Capital superscript letters indicate statistically significant differences between treatment means (ANOVA II, p ≤ 0,05). Lower case superscript letters indicate statistically significant differences between all experimental groups when a significant interaction “treatment x time” was found (ANOVA II, p ≤ 0.05 followed by multiple pairwise comparisons, Bonferroni-adjusted, p < 0.05).

Fig. 5. Relative expression of antioxidant genes in gills (left panels) and liver (right panels) of control and As-exposed zebrafish at ML (white bars) and MD (black bars): sod1, gpx7, gsr and cata. Data are shown as the mean ± SE (n = 7). Capital superscript letters indicate statistically significant differences between treatment means (ANOVA II, p ≤ 0,05). Asterisks indicate statistically significant differences between time point means (ANOVA II, p ≤ 0.05). Lower case superscript letters indicate statistically significant differences between all experimental groups when a significant interaction “treatment x time” was found (ANOVA II, p ≤ 0.05 followed by multiple pairwise comparisons, Bonferroni-adjusted, p < 0.05).

Fig. 6. Relative expression of mt2 gene in gills (left panels) and liver (right panels) of control, Hg- (A) and As-exposed (B) zebrafish at ML (white bars) and MD (black bars). Data are shown as the mean ± SE (n = 7). Graph definitions are as provided in Fig. 4.

Fig. 7. Hg concentration (mg/Kg) in liver (A), gills (B), and brain (C) of zebrafish exposed to Hg at ML (white bars) and MD (black bars) for 6 h. Graph definitions are as provided in Fig. 4.

Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Chemosphere