First published online February 20, 2004
Journal of Experimental Biology 207, 1249-1261 (2004)
Published by The Company of Biologists 2004
doi: 10.1242/jeb.00871
The physiological consequences of exposure to chronic, sublethal waterborne nickel in rainbow trout (Oncorhynchus mykiss): exercise vs resting physiology
Eric F. Pane1,*,
Aziz Haque1,
Greg G. Goss2 and
Chris M. Wood1
1 Department of Biology, McMaster University, Hamilton, Ontario, Canada, L8S
4K1
2 Department of Biological Sciences, University of Alberta, Edmonton,
Alberta, Canada, T6G 2E9

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Fig. 2. (A) Ni concentrations in various tissues of juvenile rainbow trout
following 42 days of exposure to either control (open bars), 384 µg Ni
l1 (hatched bars) or 2034 µg Ni l1
(filled bars). Values are means ±1
S.E.M. (N=610). Asterisks
indicate significant difference (P<0.05) from control mean by a
one-way ANOVA with a two-sided Dunnett's post-hoc multiple comparison
test. (B) Relative distribution of accumulated Ni among eight tissues in a
hypothetical 1-kg rainbow trout. Accumulated Ni in each tissue (µg Ni
kg1 tissue; see A) was multiplied by that tissue's relative
proportion of total body mass to normalize individual tissue Ni burdens to a
hypothetical 1-kg fish. Therefore, normalized accumulation is expressed as
µg Ni kg fish1 for each tissue. (C) Percentage of
accumulated tissue Ni burdens that can be explained purely by Ni within the
blood plasma perfusing each tissue (see Discussion for details).
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Fig. 3. Plasma ion concentrations (Na+, Cl,
Ca2+ and Mg2+) of juvenile rainbow trout following 42
days of exposure to either control (open bars), 384 µg Ni
l1 (hatched bars) or 2034 µg Ni l1
(filled bars). Values are means ±1
S.E.M. (N=610). Asterisks
indicate significant difference (P<0.05) from control mean by a
one-way ANOVA with a two-sided Dunnett's post-hoc multiple comparison
test.
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Fig. 4. Plasma stress indicators in juvenile rainbow trout following 42 days of
exposure to either control (open bars), 384 µg Ni l1
(hatched bars) or 2034 µg Ni l1 (filled bars). Values are
means ±1 S.E.M.
(N=610). Asterisks indicate significant difference
(P<0.05) from control mean by a one-way ANOVA with a two-sided
Dunnett's post-hoc multiple comparison test.
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Fig. 5. Critical swimming speed (Ucrit) of juvenile rainbow
trout following 12 days and 24 days of exposure to either control (open bars),
384 µg Ni l1 (hatched bars) or 2034 µg Ni
l1 (filled bars). Values are means ±1
S.E.M. (N=610). Asterisks
indicate significant difference (P<0.05) from control mean by a
one-way ANOVA with a two-sided Dunnett's post-hoc multiple comparison
test. BL = body lengths.
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Fig. 8. Light micrographs of the secondary lamellar structure of gills from (A)
control or (B) Ni-exposed fish (394 µg Ni l1; 69 days).
Note the thickened lamellae and decreased interlamellar water space in the
treated gill (B). Sections are 1 µm thick, stained with Richardson's stain.
Scale bars, 25 µm.
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Fig. 7. Group regressions of the log of oxygen consumption rate
(µO2) against swimming speed for which BL
represents body lengths. (A) Day 0 (initial sampling). The slopes of the two
group regression lines are not significantly different. Group regression
equations were y=0.213x+0.349, r=0.809 (control)
and y=0.206x+0.361, r=0.853 (Ni), where
y=log µO2 and x=swimming speed. (B)
Day 34 of Ni exposure. The slope of the regression line in the Ni group is
significantly different (P<0.05) from that of the control fish.
Group regression equations were y=0.270x+0.111,
r=0.869 (control) and y=0.204x+0.249,
r=0.644 (Ni). BL, body lengths.
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Fig. 9. Gill Ni concentrations in juvenile rainbow trout. Ni-exposed fish were
exposed to Ni for 99 days, followed by 38 days in clean water. Values are
means ± 1 S.E.M.
(N=69). Asterisks indicate significant difference
(P<0.05) from simultaneous control mean by an unpaired two-tailed
Student's t-test.
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© The Company of Biologists Ltd 2004