First published online January 5, 2005
Journal of Experimental Biology 208, 309-316 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01410
The influence of environmental PO2 on hemoglobin oxygen saturation in developing zebrafish Danio rerio
Sandra Grillitsch1,2,
Nikolaus Medgyesy1,2,
Thorsten Schwerte1,2 and
Bernd Pelster1,2,*
1 Institute for Zoology and Limnology, University of Innsbruck,
Austria
2 Center for Molecular Biosciences, Innsbruck, Austria

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Fig. 1. Schematic drawing of the experimental chamber with an embedded zebrafish
larva.
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Fig. 2. Maximum differences in light absorption of oxygenated and deoxygenated
zebrafish blood between 2 d.p.f. and 12 d.p.f. Values are means ±
S.E.M.; N values are given in parentheses above each
symbol.
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Fig. 3. (A) Number of zebrafish larvae showing partial deoxygenation of the blood
under normoxic conditions (filled bar) and the number of animals, showing
complete oxygen saturation (open bar). (B) Oxygen saturation of the blood in
the ventricle of normoxic zebrafish larvae
(PO2=20 kPa). Values are means ±
S.E.M. *Significant differences from full saturation.
N values are given in parentheses below each symbol.
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Fig. 4. Oxygenation of blood in the ventricle under progressive hypoxia in 2 d.p.f.
animals (N=12) and at 8 d.p.f. (N=8);
*Significant differences from control values recorded at normoxia
(PO2=20 kPa).
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Fig. 5. Heart rate of zebrafish larvae between 2 d.p.f. and 12 d.p.f. under
normoxic (PO2=20 kPa) and hyperoxic
(PO2=100 kPa) conditions. Values are means
± S.E.M.; *Significant differences between
normoxia and hyperoxia (P<0.05). N values are given in
parentheses below each symbol.
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Fig. 6. Heart rate of zebrafish larvae between 2 d.p.f. and 12 d.p.f. under
normoxic conditions (PO2=20 kPa) and
progressive hypoxia down to anoxic conditions. Values are means ±
S.E.M. *Significant differences between normoxia and
hypoxic conditions (P<0.05). N values are given in
parentheses below each symbol.
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© The Company of Biologists Ltd 2005