Growth and metabolism of larval zebrafish: effects of swim training
B. Bagatto1,*,
B. Pelster2 and
W. W. Burggren1
1 Department of Biological Sciences, University of North Texas, Denton, Texas, 76203, USA and
2 Institut fur Zoologie und Limnoligie, University of Innsbruck, 6020 Innsbruck, Austria

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Fig. 1. Survival of zebrafish yolk-sac larvae (day 4), swim-up larvae (day 9), and free-swimming larvae (day 21), at the conclusion of a training period. Circles, control group; triangles, larvae training at 2 BL s1; squares, larvae training at 5 BL s1. Open symbols indicate a value significantly different from the corresponding control value. Values are means ± 1 S.E.M.; N=120 for each treatment group at the beginning of the treatment.
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Fig. 2. Yolk-sac volume in day-4 zebrafish larvae exposed to training at 2 BL s1 and 5 BL s1. Diamond, starting point; circles, control group; triangles, larvae training at 2 BL s1; squares, larvae training at 5 BL s1. An open symbol indicates a value significantly different from the corresponding control value. Values are means ± 1 S.E.M.; N=10 for each group.
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Fig. 4. Active mass-specific oxygen consumption ( O2a,m) (A) and locomotion efficiency (nmol O2 mg1 m1) (B) in free-swimming zebrafish (day 21) as a function of water velocity. Larvae were measured after the 11-day experimental period of either no training or training at 5 BL s1. Open symbols indicate that the regression line is significantly different from the control (filled circles).
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Fig. 5. Critical PO2 (Pcrit) and critical debilitation PO2 (Pd) of zebrafish yolk-sac larvae (day 4), swim-up larvae (day 9), and free-swimming larvae (day 21), exposed to training. Circles, control groups; squares, larvae training at 5 BL s1. An open symbol indicates a value significantly different from the corresponding control value. Values are means ± 1 S.E.M.; N=8 for each group.
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© The Company of Biologists Ltd 2001