spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Josephson, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Josephson, R.

Journal of Experimental Biology, Vol 200, Issue 8 1227-1239, Copyright © 1997 by Company of Biologists


JOURNAL ARTICLES

Power output from a flight muscle of the bumblebee Bombus terrestris. II. Characterization of the parameters affecting power output

R Josephson

1. Length-tension relationships and work output were investigated in the intact, dorso-ventral flight muscle of the bumblebee Bombus terrestris. The muscle is an asynchronous muscle. Like other asynchronous flight muscles, it has high resting stiffness and produces relatively low active force in response to tetanic stimulation. 2. The muscle shows shortening deactivation and stretch activation, properties that result in delayed force changes in response to step changes in length, a phase lag between force and length during imposed sinusoidal strain and, under appropriate conditions, positive work output during oscillatory length change. 3. Work loops were used to quantify work output by the muscle during imposed sinusoidal oscillation. The curves relating net work per cycle with muscle length, oscillatory strain and oscillatory frequency were all roughly bell-shaped. The work-length curve was narrow. The optimum strain for net work per cycle was approximately 3 %, which is probably somewhat greater than the strain experienced by the muscle in an intact, flying bumblebee. The optimum frequency for net work output per cycle was 63 Hz (30 °C). The optimum frequency for power output was 73 Hz, which agrees well with the normal wing stroke frequency if allowance is made for the elevated temperature (approximately 40 °C) in the thorax of a flying bumblebee. The optimal strain for work output was not strongly dependent on oscillation frequency. 4. Resilience (that is the work output during shortening/work input during lengthening) for unstimulated muscle and dynamic stiffness (=stress/strain) for both stimulated and unstimulated muscles were determined using the strain (3 %) and oscillation frequency (64 Hz) which maximized work output in stimulated muscles. Unstimulated muscle is a good energy storage device. Its resilience increased with increasing muscle length (and increasing resting force) to reach values of over 90 %. The dynamic stiffness of both stimulated and unstimulated muscles increased with muscle length, but the increase was relatively greater in unstimulated muscle, and at long muscle lengths the stiffness of unstimulated muscle exceeded that of stimulated muscle. Effectively, dynamic stiffness is reduced by stimulation! This is taken as indicating that part of the stiffness in an unstimulated muscle reflects structures, possibly attached cross bridges, whose properties change upon stimulation.


This article has been cited by other articles:


Home page
J. Exp. Biol.Home page
T. E. Higham and A. A. Biewener
Integration within and between muscles during terrestrial locomotion: effects of incline and speed
J. Exp. Biol., July 15, 2008; 211(14): 2303 - 2316.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
W. A. Woods Jr, S. J. Fusillo, and B. A. Trimmer
Dynamic properties of a locomotory muscle of the tobacco hornworm Manduca sexta during strain cycling and simulated natural crawling
J. Exp. Biol., March 15, 2008; 211(6): 873 - 882.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
B. C. W. Tanner, M. Regnier, and T. L. Daniel
A spatially explicit model of muscle contraction explains a relationship between activation phase, power and ATP utilization in insect flight
J. Exp. Biol., January 15, 2008; 211(2): 180 - 186.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
M. S. Tu and T. L. Daniel
Submaximal power output from the dorsolongitudinal flight muscles of the hawkmoth Manduca sexta
J. Exp. Biol., December 15, 2004; 207(26): 4651 - 4662.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
A. N. Ahn and R. J. Full
A motor and a brake: two leg extensor muscles acting at the same joint manage energy differently in a running insect
J. Exp. Biol., February 1, 2002; 205(3): 379 - 389.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
R. Josephson, J. Malamud, and D. Stokes
Power output by an asynchronous flight muscle from a beetle
J. Exp. Biol., January 9, 2000; 203(17): 2667 - 2689.
[Abstract] [PDF]


Home page
J. Exp. Biol.Home page
R. Josephson, J. Malamud, and D. Stokes
Asynchronous muscle: a primer
J. Exp. Biol., January 9, 2000; 203(18): 2713 - 2722.
[Abstract] [PDF]


Home page
J. Exp. Biol.Home page
R. Josephson and D. Stokes
Work-dependent deactivation of a crustacean muscle
J. Exp. Biol., January 9, 1999; 202(18): 2551 - 2565.
[Abstract] [PDF]




© The Company of Biologists Ltd 1997