Oxygen uptake during post dive recovery in a diving bird Aythya fuligula: implications for optimal foraging models
Roland Parkes1,
Lewis G. Halsey1,*,
Anthony J. Woakes1,
Roger L. Holder2 and
Patrick J. Butler1
1 School of Biosciences, University of Birmingham, Edgbaston, Birmingham,
B15 2TT, UK
2 School of Mathematics and Statistics, University of Birmingham, Edgbaston,
Birmingham, B15 2TT, UK

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Fig. 1. The optimal breathing model (Kramer,
1988 ). The abscissa shows time spent travelling to and from the
foraging site to the left of the ordinate, and time at the surface to the
right. The ordinate shows the amount of oxygen consumed during travel and
gained during surface periods. The value ts*
denotes the optimal surface time for the diver, according to the model, in
terms of maximising the proportion of time at the foraging site.
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Fig. 2. Model, as in Fig. 1,
incorporating a biphasic oxygen uptake curve
(Walton et al., 1998 ). Due to
the initial rapid resaturation of oxygen into the respiratory oxygen stores
upon surfacing, a biphasic oxygen resaturation curve means that a range of
dive depths (d1-d3), associated with travel time
(tT), have identical optimal surface times
(ts*).
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Fig. 3. Diagram of the experimental apparatus showing a tufted duck in an enclosed
section of a large dive tank. For further details, see Materials and
methods.
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Fig. 4. Charts to show the methodology of biphasic modelling using broken stick
analysis. (A) VO2 data for four tufted ducks
were smoothed and plotted on a logarithmic axis. The break point was
arbitrarily chosen at 6 s. Linear regression was performed up to and including
the break point (Linear phase 1) and also on all remaining data points (Linear
phase 2). Regression parameters were then used to determine the point of
inflection (C) where the two lines intersect. (B)
VO2 data for four tufted ducks were regressed
onto the two regression lines shown (biphasic and linear). The biphasic
regression line was calculated as shown in Fig. 4A. Commonly in this type of
analysis the biphasic point of inflection (C) was not identical to
the selected break point.
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Fig. 5. Bar chart showing mean oxygen uptake for four tufted ducks during the first
14.5 s post surface (values are means + S.E.M.). The line graphs show the
cumulative oxygen gain curve for short (<16.0 s; solid line) and long dives
( 16.0 s; broken line) for the first 14.5 s post dive.
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Fig. 6. Comparison of the mean oxygen uptake curve of four tufted ducks at 5 s, 10
s and 15 s surface duration ± S.E.M. after short dives and long
dives.
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Fig. 7. Histogram showing the calculated residual variances with the break point
every 0.25 s for the first 6 s post dive for long dives of four tufted ducks.
The break point with the lowest residual variance occurred 3.00 s post dive
and was used to define the biphasic regression line. See statistics in
Materials and methods for details of the biphasic determination.
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Fig. 8. Chart to show biphasic modelling for long duration dives during the first
15 s post surface for four tufted ducks. The smoothed
VO2 data (open circles) have been
log-transformed. Least-squares regression is then performed using the linear
and the biphasic regression lines. Phases 1 and 2 of the biphasic regression
line can be seen with the point of inflection at 3.28 s post surface.
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Fig. 9. Mean VO2 observed after long dives of four
tufted ducks. Data were smoothed by taking a three-point moving average. As
well as the general exponential decrease in VO2
over the first 15 s post surface, there is a cyclical aspect to the data. This
is highlighted subjectively on the graph (black bars), and is believed to
correspond to expiration (peak) and inspiration (trough), occurring at
frequencies similar to those recorded by Butler and Woakes
(1979 ) in a diving pochard
(Aythya ferina). The arrow indicates the point of inflection for
biphasic uptake.
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© The Company of Biologists Ltd 2002