|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Journal of Experimental Biology, Vol 200, Issue 5 921-929, Copyright © 1997 by Company of Biologists
JOURNAL ARTICLES |
P Chai, JS Chen and R Dudley
Department of Zoology, University of Texas, Austin 78712, USA. pengchai@utxvms.cc.utexas.edu
Maximal load-lifting capacities of six ruby-throated hummingbirds (Archilochus colubris) were determined under conditions of burst performance. Mechanical power output under maximal loading was then compared with maximal hovering performance in hypodense gas mixtures of normodense air and heliox. The maximal load lifted was similar at air temperatures of 5 and 25 degrees C, and averaged 80% of body mass. The duration of load-lifting was brief, of the order of 1 s, and was probably sustained via phosphagen substrates. Under maximal loading, estimates of muscle mass-specific mechanical power output assuming perfect elastic energy storage averaged 206 W kg-1, compared with 94 W kg-1 during free hovering without loading. Under conditions of limiting performance in hypodense mixtures, maximal mechanical power output was much lower (131 W kg-1, five birds) but was sustained for longer (4 s), demonstrating an inverse relationship between the magnitude and duration of maximum power output. In free hovering flight, stroke amplitude and wingbeat frequency varied in inverse proportion between 5 and 25 degrees C, suggesting thermoregulatory contributions by the flight muscles. Stroke amplitude under conditions of maximal loading reached a geometrical limit at slightly greater than 180 degrees. Previous studies of maximum performance in flying animals have estimated mechanical power output using a simplified actuator disk model without a detailed knowledge of wingbeat frequency and stroke amplitude. The present load-lifting results, together with actuator disc estimates of induced power derived from hypodense heliox experiments, are congruent with previous load-lifting studies of maximum flight performance. For ruby-throated hummingbirds, the inclusion of wingbeat frequency and stroke amplitude in a more detailed aerodynamic model of hovering yields values of mechanical power output 34% higher than previous estimates. More generally, the study of performance limits in flying animals necessitates careful specification of behavioral context as well as quantitative determination of wing and body kinematics.
This article has been cited by other articles:
![]() |
B. W. Tobalske, D. R. Warrick, C. J. Clark, D. R. Powers, T. L. Hedrick, G. A. Hyder, and A. A. Biewener Three-dimensional kinematics of hummingbird flight J. Exp. Biol., July 1, 2007; 210(13): 2368 - 2382. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. C. Welch Jr, D. L. Altshuler, and R. K. Suarez Oxygen consumption rates in hovering hummingbirds reflect substrate-dependent differences in P/O ratios: carbohydrate as a `premium fuel' J. Exp. Biol., June 15, 2007; 210(12): 2146 - 2153. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. L. Altshuler, R. Dudley, and J. A. McGuire Resolution of a paradox: Hummingbird flight at high elevation does not come without a cost PNAS, December 21, 2004; 101(51): 17731 - 17736. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. E. Dillon and R. Dudley Allometry of maximum vertical force production during hovering flight of neotropical orchid bees (Apidae: Euglossini) J. Exp. Biol., February 1, 2004; 207(3): 417 - 425. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. J. Irschick, B. Vanhooydonck, A. Herrel, and A. Andronescu Effects of loading and size on maximum power output and gait characteristics in geckos J. Exp. Biol., November 15, 2003; 206(22): 3923 - 3934. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. L. Altshuler and R. Dudley Kinematics of hovering hummingbird flight along simulated and natural elevational gradients J. Exp. Biol., September 15, 2003; 206(18): 3139 - 3147. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Dudley and Y. Winter Hovering flight mechanics of neotropical flower bats (Phyllostomidae: Glossophaginae) in normodense and hypodense gas mixtures J. Exp. Biol., December 1, 2002; 205(23): 3669 - 3677. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. L. Altshuler and R. Dudley The ecological and evolutionary interface of hummingbird flight physiology J. Exp. Biol., August 15, 2002; 205(16): 2325 - 2336. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. N. Askew and R. L. Marsh Muscle designed for maximum short-term power output: quail flight muscle J. Exp. Biol., August 1, 2002; 205(15): 2153 - 2160. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Dudley Mechanisms and Implications of Animal Flight Maneuverability Integr. Comp. Biol., February 1, 2002; 42(1): 135 - 140. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. N. Askew, R. L. Marsh, and C. P. Ellington The mechanical power output of the flight muscles of blue-breasted quail (Coturnix chinensis) during take-off J. Exp. Biol., January 11, 2001; 204(21): 3601 - 3619. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Roberts and J. Harrison Mechanisms of thermal stability during flight in the honeybee apis mellifera J. Exp. Biol., January 6, 1999; 202(11): 1523 - 1533. [Abstract] [PDF] |
||||