First published online June 11, 2007
Journal of Experimental Biology 210, 2146-2153 (2007)
Published by The Company of Biologists 2007
doi: 10.1242/jeb.005389
Oxygen consumption rates in hovering hummingbirds reflect substrate-dependent differences in P/O ratios: carbohydrate as a `premium fuel'
Kenneth C. Welch, Jr1,*,
Douglas L. Altshuler2 and
Raul K. Suarez1
1 Department of Ecology, Evolution and Marine Biology, University of
California, Santa Barbara, CA 93106-9610, USA
2 Department of Biology, University of California, Riverside, CA 92521,
USA

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Fig. 1. Mass-specific oxygen consumption rate
( O2/Mb)
in relation to respiratory quotient (RQ) in (A) Anna's (C. anna) and
(B) rufous hummingbirds (S. rufus).
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Fig. 2. Oxygen consumption rate per unit hovering power output
( O2/W) in
relation to respiratory quotient (RQ) in Anna's hummingbirds (C.
anna) assuming (A) perfect (Pper) or (B) zero
(Pzero) elastic storage.
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Fig. 3. Oxygen consumption rate per unit hovering power output
( O2/W) in
relation to respiratory quotient (RQ) in rufous hummingbirds (S.
rufus) assuming (A) perfect (Pper) or (B) zero
(Pzero) elastic storage.
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Fig. 4. The relationship between whole-animal oxygen consumption rate
( O2; ml
O2 h1) and whole-animal ATP turnover rate per
unit power output (mmol ATP h1 W1,
assuming either perfect, Pper, or zero,
Pzero, elastic storage) to respiratory quotient (RQ). The
slope of whole-animal
O2 in relation
to RQ is significantly different from zero (F1,22=10.4134,
P=0.0039). The slopes of whole-animal ATP turnover rate per unit
power output in relation to RQ are not significantly different from zero
(assuming Pper, F1,22=1.8537,
P=0.1871; assuming Pzero,
F1,22=1.1524, P=0.2947). Note that >90% of
O2 and ATP
turnover rate during hovering are accounted for by flight muscles. Example
using Anna's hummingbird (C. anna) number 3.
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© The Company of Biologists Ltd 2007