First published online July 6, 2005
Journal of Experimental Biology 208, 2693-2705 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01678
Alkaline tide and nitrogen conservation after feeding in an elasmobranch (Squalus acanthias)
Chris M. Wood1,2,3,*,
Makiko Kajimura1,3,
Thomas P. Mommsen3,4 and
Patrick J. Walsh2,3
1 Department of Biology, McMaster University, 1280 Main St West, Hamilton,
Ontario, Canada L8S 4K1
2 Rosenstiel School of Marine and Atmospheric Sciences, University of Miami,
Miami, Florida 33149, USA
3 Bamfield Marine Sciences Centre, 100 Pachena Drive, Bamfield, British
Columbia, Canada V0R 1B0
4 Department of Biology, University of Victoria, Victoria, British Columbia,
Canada V8W 2N5

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Fig. 1. The influence of (A) the control treatment or (B) experimental feeding on
arterial pH (pHa; circles) and venous pH (pHv; triangles) in Squalus
acanthias of Series 1. The experimental meal was 20 g of flatfish muscle
paste in 20 ml of 140 mmol l1 NaCl saline per kg dogfish,
administered as a bolus down the stomach tube at time 0 h. The control
treatment was comparable gastric loading of 40 ml of 140 mmol
l1 NaCl saline per kg dogfish. Values are means ± 1
S.E.M. (N=5). P represents the
pre-feeding measurement (horizontal dotted lines). The overall influence of
experimental feeding was significant for both pHa and pHv (two-way ANOVA,
P x0.05). Within each treatment, means not sharing the same
letter are significantly different (one way ANOVA followed by the LSD test).
Asterisks indicate significant differences between control and experimental
treatments for the same parameter at the same time.
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Fig. 2. The influence of (A) the control treatment or (B) experimental feeding on
arterial true plasma bicarbonate ([HCO3]a;
circles) and venous true plasma bicarbonate
([HCO3]v; triangles) concentrations in
Squalus acanthias of Series 1. Values are means ± 1
S.E.M. (N=5). Other details as in
legend of Fig. 1. The overall
influence of experimental feeding was significant for both
[HCO3]a and [HCO3]v
(two-way ANOVA, P x0.05).
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Fig. 5. The influence of (A) the control treatment or (B) experimental feeding on
the rate of ammonia-N excretion in Squalus acanthias of Series 2.
Other details as in legend of Fig.
1. There was a significant overall influence of experimental
feeding (two-way ANOVA, P x0.05). There were no significant
differences between control and experimental treatments at the same time.
Values are means ± 1 S.E.M. Data were
taken from those dogfish of Series 2 (control N=5, experimental
N=4) where there was no struggling or potential for blood loss from
fin abrasion.
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Fig. 6. The influence of (A) the control treatment or (B) experimental feeding on
the rate of urea-N excretion in Squalus acanthias of Series 2. Values
are means ± 1 S.E.M. (control
N=5, experimental N=4). Other details as in legends of Figs
1 and
5. There was no significant
overall influence of experimental feeding (two-way ANOVA, P>0.05).
There were no significant differences between control and experimental
treatments at the same time.
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Fig. 7. The influence of experimental feeding (triangles) or the control treatment
(circles) on (A) plasma urea-N (B) plasma ammonia-N and (C) plasma
trimethylamine oxide-N (TMAO-N) concentrations in Squalus acanthias
of Series 2. Note the different units (µmol l1 for
ammonia-N versus mmol l1 for urea-N and TMAO-N).
Values are means ± 1 S.E.M.
(N=8). Other details as in legend of
Fig. 1. There was a significant
overall influence of experimental feeding only on plasma ammonia-N (two-way
ANOVA, P x0.05) but not on plasma urea-N or TMAO-N.
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Fig. 8. The influence of experimental feeding (triangles) or the control treatment
(circles) on (A) plasma osmolality and (B) plasma chloride concentration in
Squalus acanthias of Series 2. Values are means ± 1
S.E.M. (N=8). Other details as in
legend of Fig. 1. There were
significant overall influences of experimental feeding on both osmolality and
chloride (two-way ANOVA, P x0.05).
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© The Company of Biologists Ltd 2005