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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
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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


Figure 1
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Fig. 1. Mass-specific oxygen consumption rate (VO2/Mb) in relation to respiratory quotient (RQ) in (A) Anna's (C. anna) and (B) rufous hummingbirds (S. rufus).

 

Figure 2
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Fig. 2. Oxygen consumption rate per unit hovering power output (VO2/W) in relation to respiratory quotient (RQ) in Anna's hummingbirds (C. anna) assuming (A) perfect (Pper) or (B) zero (Pzero) elastic storage.

 

Figure 3
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Fig. 3. Oxygen consumption rate per unit hovering power output (VO2/W) in relation to respiratory quotient (RQ) in rufous hummingbirds (S. rufus) assuming (A) perfect (Pper) or (B) zero (Pzero) elastic storage.

 

Figure 4
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Fig. 4. The relationship between whole-animal oxygen consumption rate (VO2; ml O2 h–1) and whole-animal ATP turnover rate per unit power output (mmol ATP h–1 W–1, assuming either perfect, Pper, or zero, Pzero, elastic storage) to respiratory quotient (RQ). The slope of whole-animal VO2 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 VO2 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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