scholarly journals Short Communication: Maximum Load-Lifting and Induced Power Output of Harris' Hawks are General Functions of Flight Muscle Mass

1990 ◽  
Vol 149 (1) ◽  
pp. 511-514 ◽  
Author(s):  
JAMES H. MARDEN
Keyword(s):  
Muscle Mass ◽  
Power Output ◽  
Short Communication ◽  
Flight Muscle ◽  
Maximum Load

scholarly journals Alterations in flight muscle ultrastructure and function in Drosophila tropomyosin mutants.

1996 ◽  
Vol 135 (3) ◽  
pp. 673-687 ◽  
Author(s):  
A J Kreuz ◽  
A Simcox ◽  
D Maughan
Keyword(s):  
Amino Acid ◽  
Power Output ◽  
Flight Muscle ◽  
Structure And Function ◽  
Wild Type ◽  
Muscle Tropomyosin ◽  
Ultrastructure And Function ◽  
And Function ◽  
Net Power Output ◽  
Current Report

Drosophila indirect flight muscle (IFM) contains two different types of tropomyosin: a standard 284-amino acid muscle tropomyosin, Ifm-TmI, encoded by the TmI gene, and two > 400 amino acid tropomyosins, TnH-33 and TnH-34, encoded by TmII. The two IFM-specific TnH isoforms are unique tropomyosins with a COOH-terminal extension of approximately 200 residues which is hydrophobic and rich in prolines. Previous analysis of a hypomorphic TmI mutant, Ifm(3)3, demonstrated that Ifm-TmI is necessary for proper myofibrillar assembly, but no null TmI mutant or TmII mutant which affects the TnH isoforms have been reported. In the current report, we show that four flightless mutants (Warmke et al., 1989) are alleles of TmI, and characterize a deficiency which deletes both TmI and TmII. We find that haploidy of TmI causes myofibrillar disruptions and flightless behavior, but that haploidy of TmII causes neither. Single fiber mechanics demonstrates that power output is much lower in the TmI haploid line (32% of wild-type) than in the TmII haploid line (73% of wild-type). In myofibers nearly depleted of Ifm-TmI, net power output is virtually abolished (< 1% of wild-type) despite the presence of an organized fibrillar core (approximately 20% of wild-type). The results suggest Ifm-TmI (the standard tropomyosin) plays a key role in fiber structure, power production, and flight, with reduced Ifm-TmI expression producing corresponding changes of IFM structure and function. In contrast, reduced expression of the TnH isoforms has an unexpectedly mild effect on IFM structure and function.

Body and organ mass dynamics during remigial moult in a wing–foot-propelled diving sea duck: the Common Eider (Atlantic) (Somateria mollissima dresseri)

2015 ◽  
Vol 93 (10) ◽  
pp. 755-764 ◽  
Author(s):  
A. Viain ◽  
M. Guillemette ◽  
J.-P.L. Savard
Keyword(s):  
Muscle Mass ◽  
Body Mass ◽  
Flight Muscle ◽  
Somateria Mollissima ◽  
Dabbling Ducks ◽  
Diving Ducks ◽  
Common Eiders ◽  
Sea Duck ◽  
Remigial Moult ◽  
Atrophy Of The Heart

Body and organ dynamics, during remigial moult, have been mainly explored on geese, dabbling ducks, and foot-propelled diving ducks, but weakly on sea ducks. This study investigated the internal changes in a wing–foot-propelled sea duck to determine the adaptive strategies implemented. Forty-five male Common Eiders (Atlantic) (Somateria mollissima dresseri Sharpe, 1871), collected in the Gulf of St. Lawrence, were dissected; their body mass, muscle mass, and organ sizes were measured. We tested three hypotheses: (1) S. m. dresseri use a strategic reduction of body mass to reduce the flightlessness duration; (2) organs will exhibit changes consistent with a trade-off between function and maintenance to save and reallocate energy and proteins to feather growth; (3) S. m. dresseri would show lower flight muscle reduction than foot-propelled diving ducks. Somateria mollissima dresseri did not lose body mass, which does not support the first hypothesis. Atrophy of the heart followed by hypertrophy and opposite changes in leg muscle mass and gizzard mass are consistent with the second hypothesis. Flight muscle mass showed lower variations than in other ducks, validating the third hypothesis. We also suggest that the lipid depletion observed early in the moult could be a strategy to reduce foraging effort and minimize the risk of damaging the growing feathers.

Dynamics of in vivo power output and efficiency of Nasonia asynchronous flight muscle

2006 ◽  
Vol 124 (1) ◽  
pp. 93-107 ◽  
Author(s):  
Fritz-Olaf Lehmann ◽  
Nicole Heymann
Keyword(s):  
Power Output ◽  
Flight Muscle

Power output by an asynchronous flight muscle from a beetle

2000 ◽  
Vol 203 (17) ◽  
pp. 2667-2689 ◽  
Author(s):  
R.K. Josephson ◽  
J.G. Malamud ◽  
D.R. Stokes
Keyword(s):  
Power Output ◽  
Flight Muscle ◽  
Muscle Length ◽  
Mechanical Power ◽  
Effect Of Temperature ◽  
Muscle Temperature ◽  
Work Output ◽  
Stroke Frequency ◽  
Mechanical Power Output ◽  
Wing Stroke

The basalar muscle of the beetle Cotinus mutabilis is a large, fibrillar flight muscle composed of approximately 90 fibers. The paired basalars together make up approximately one-third of the mass of the power muscles of flight. Changes in twitch force with changing stimulus intensity indicated that a basalar muscle is innervated by at least five excitatory axons and at least one inhibitory axon. The muscle is an asynchronous muscle; during normal oscillatory operation there is not a 1:1 relationship between muscle action potentials and contractions. During tethered flight, the wing-stroke frequency was approximately 80 Hz, and the action potential frequency in individual motor units was approximately 20 Hz. As in other asynchronous muscles that have been examined, the basalar is characterized by high passive tension, low tetanic force and long twitch duration. Mechanical power output from the basalar muscle during imposed, sinusoidal strain was measured by the work-loop technique. Work output varied with strain amplitude, strain frequency, the muscle length upon which the strain was superimposed, muscle temperature and stimulation frequency. When other variables were at optimal values, the optimal strain for work per cycle was approximately 5%, the optimal frequency for work per cycle approximately 50 Hz and the optimal frequency for mechanical power output 60–80 Hz. Optimal strain decreased with increasing cycle frequency and increased with muscle temperature. The curve relating work output and strain was narrow. At frequencies approximating those of flight, the width of the work versus strain curve, measured at half-maximal work, was 5% of the resting muscle length. The optimal muscle length for work output was shorter than that at which twitch and tetanic tension were maximal. Optimal muscle length decreased with increasing strain. The curve relating work output and muscle length, like that for work versus strain, was narrow, with a half-width of approximately 3 % at the normal flight frequency. Increasing the frequency with which the muscle was stimulated increased power output up to a plateau, reached at approximately 100 Hz stimulation frequency (at 35 degrees C). The low lift generated by animals during tethered flight is consistent with the low frequency of muscle action potentials in motor units of the wing muscles. The optimal oscillatory frequency for work per cycle increased with muscle temperature over the temperature range tested (25–40 degrees C). When cycle frequency was held constant, the work per cycle rose to an optimum with increasing temperature and then declined. We propose that there is a temperature optimum for work output because increasing temperature increases the shortening velocity of the muscle, which increases the rate of positive work output during shortening, but also decreases the durations of the stretch activation and shortening deactivation that underlie positive work output, the effect of temperature on shortening velocity being dominant at lower temperatures and the effect of temperature on the time course of activation and deactivation being dominant at higher temperatures. The average wing-stroke frequency during free flight was 94 Hz, and the thoracic temperature was 35 degrees C. The mechanical power output at the measured values of wing-stroke frequency and thoracic temperature during flight, and at optimal muscle length and strain, averaged 127 W kg(−1)muscle, with a maximum value of 200 W kg(−1). The power output from this asynchronous flight muscle was approximately twice that measured with similar techniques from synchronous flight muscle of insects, supporting the hypothesis that asynchronous operation has been favored by evolution in flight systems of different insect groups because it allows greater power output at the high contraction frequencies of flight.

scholarly journals The weak link: do muscle properties determine locomotor performance in frogs?

2011 ◽  
Vol 366 (1570) ◽  
pp. 1488-1495 ◽  
Author(s):  
Thomas J. Roberts ◽  
Emily M. Abbott ◽  
Emanuel Azizi
Keyword(s):  
Muscle Mass ◽  
Power Output ◽  
Muscle Power ◽  
Locomotor Performance ◽  
Jump Performance ◽  
Leopard Frogs ◽  
Ideal System ◽  
Mechanical Power Output ◽  
Osteopilus Septentrionalis ◽  
Jump Power

Muscles power movement, yet the conceptual link between muscle performance and locomotor performance is poorly developed. Frog jumping provides an ideal system to probe the relationship between muscle capacity and locomotor performance, because a jump is a single discrete event and mechanical power output is a critical determinant of jump distance. We tested the hypothesis that interspecific variation in jump performance could be explained by variability in available muscle power. We used force plate ergometry to measure power produced during jumping in Cuban tree frogs ( Osteopilus septentrionalis ), leopard frogs ( Rana pipiens ) and cane toads ( Bufo marinus ). We also measured peak isotonic power output in isolated plantaris muscles for each species. As expected, jump performance varied widely. Osteopilus septentrionalis developed peak power outputs of 1047.0 ± 119.7 W kg −1 hindlimb muscle mass, about five times that of B. marinus (198.5 ± 54.5 W kg −1 ). Values for R. pipiens were intermediate (543.9 ± 96.2 W kg −1 ). These differences in jump power were not matched by differences in available muscle power, which were 312.7 ± 28.9, 321.8 ± 48.5 and 262.8 ± 23.2 W kg −1 muscle mass for O. septentrionalis , R. pipiens and B. marinus , respectively. The lack of correlation between available muscle power and jump power suggests that non-muscular mechanisms (e.g. elastic energy storage) can obscure the link between muscle mechanical performance and locomotor performance.

The effects of octopamine on contraction kinetics and power output of a locust flight muscle

1988 ◽  
Vol 162 (6) ◽  
pp. 827-835 ◽  
Author(s):  
Jean G. Malamud ◽  
Andrew P. Mizisin ◽  
Robert K. Josephson
Keyword(s):  
Power Output ◽  
Flight Muscle ◽  
Locust Flight ◽  
Contraction Kinetics

scholarly journals Multicomponent exercises including muscle power training enhance muscle mass, power output, and functional outcomes in institutionalized frail nonagenarians

AGE ◽  
2013 ◽  
Vol 36 (2) ◽  
pp. 773-785 ◽  
Author(s):  
Eduardo L. Cadore ◽  
Alvaro Casas-Herrero ◽  
Fabricio Zambom-Ferraresi ◽  
Fernando Idoate ◽  
Nora Millor ◽  
...  
Keyword(s):  
Muscle Mass ◽  
Power Output ◽  
Functional Outcomes ◽  
Muscle Power ◽  
Power Training
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