PECTORALIS MUSCLE FORCE AND POWER OUTPUT DURING DIFFERENT MODES OF FLIGHT IN PIGEONS (COLUMBA LIVIA)

1993 ◽  
Vol 176 (1) ◽  
pp. 31-54 ◽  
Author(s):  
K. P. Dial ◽  
A. A. Biewener

In vivo measurements of pectoralis muscle force during different modes of free flight (takeoff, level flapping, landing, vertical ascending and near vertical descending flight) were obtained using a strain gauge attached to the dorsal surface of the delto-pectoral crest (DPC) of the humerus in four trained pigeons (Columba livia). In one bird, a rosette strain gauge was attached to the DPC to determine the principal axis of strain produced by tension of the pectoralis. Strain signals recorded during flight were calibrated to force based on in situ measurements of tetanic force and on direct tension applied to the muscle's insertion at the DPC. Rosette strain recordings showed that at maximal force the orientation of tensile principal strain was −15° (proximo-anterior) to the perpendicular axis of the DPC (or +75° to the longitudinal axis of the humerus), ranging from +15 to −25° to the DPC axis during the downstroke. The consistency of tensile principal strain orientation in the DPC confirms the more general use of single-element strain gauges as being a reliable method for determining in vivo pectoralis force generation. Our strain recordings show that the pectoralis begins to develop force as it is being lengthened, during the final one-third of the upstroke, and attains maximum force output while shortening during the first one-third of the downstroke. Force is sustained throughout the entire downstroke, even after the onset of the upstroke for certain flight conditions. Mean peak forces developed by the pectoralis based on measurements from 40 wingbeats for each bird (160 total) were: 24.9+/−3.1 N during takeoff, 19.7+/−2.0 N during level flight (at speeds of about 6–9 m s-1 and a wingbeat frequency of 8.6+/−0.3 Hz), 18.7+/−2.5 N during landing, 23.7+/−2.7 N during near-vertical descent, and 26.0+/−1.8 N during vertical ascending flight. These forces are considerably lower than the maximum isometric force (67 N, P0) of the muscle, ranging from 28 % (landing) to 39 % (vertical ascending) of P0. Based on estimates of muscle fiber length change determined from high- speed (200 frames s-1) light cine films taken of the animals, we calculate the mass-specific power output of the pigeon pectoralis to be 51 W kg-1 during level flight (approximately 8 m s-1), and 119 W kg-1 during takeoff from the ground. When the birds were harnessed with weighted backpacks (50 % and 100 % of body weight), the forces generated by the pectoralis did not significantly exceed those observed in unloaded birds executing vertical ascending flight. These data suggest that the range of force production by the pectoralis under these differing conditions is constrained by the force- velocity properties of the muscle operating at fairly rapid rates of shortening (4.4 fiber lengths s-1 during level flight and 6.7 fiber lengths s-1 during takeoff).

1992 ◽  
Vol 164 (1) ◽  
pp. 1-18 ◽  
Author(s):  
ANDREW A. BIEWENER ◽  
KENNETH P. DIAL ◽  
G. E. GOSLOW

Force recordings of the pectoralis muscle of European starlings have been made in vivo during level flight in a wind tunnel, based on bone strain recordings at the muscle's attachment site on the humerus (deltopectoral crest). This represents the first direct measurement of muscle force during activity in a live animal based on calibrated bone strain recordings. Our force measurements confirm earlier electromyographic data and show that the pectoralis begins to develop force during the final one-third of the upstroke, reaches a maximal level halfway through the downstroke, and sustains force throughout the downstroke. Peak forces generated by the pectoralis during level flight at a speed estimated to be 13.7ms−1 averaged 6.4N (28% of maximal isometric force), generating a mean mass-specific muscle power output of 104 W kg−1. Combining our data for the power output of the pectoralis muscle with data for the metabolic power of starlings flying at a similar speed yields an overall flight efficiency of 13 %. The force recordings and length changes of the muscle, based on angular displacements of the humerus, indicate that the pectoralis muscle undergoes a lengthening--shortening contraction sequence during its activation and that, in addition to lift and thrust generation, overcoming wing inertia is probably an important function of this muscle in flapping flight.


2001 ◽  
Vol 204 (3) ◽  
pp. 495-507 ◽  
Author(s):  
M.R. Williamson ◽  
K.P. Dial ◽  
A.A. Biewener

In vivo measurements of pectoralis muscle length change and force production were obtained using sonomicrometry and delto-pectoral bone strain recordings during ascending and slow level flight in mallards (Anas platyrhynchos). These measurements provide a description of the force/length properties of the pectoralis under dynamic conditions during two discrete flight behaviors and allow an examination of the effects of differences in body size and morphology on pectoralis performance by comparing the results with those of a recent similar study of slow level flight in pigeons (Columbia livia). In the present study, the mallard pectoralis showed a distinct pattern of active lengthening during the upstroke. This probably enhances the rate of force generation and the magnitude of the force generated and, thus, the amount of work and power produced during the downstroke. The power output of the pectoralis averaged 17.0 W kg(−)(1)body mass (131 W kg(−)(1)muscle mass) during slow level flight (3 m s(−)(1)) and 23.3 W kg(−)(1)body mass (174 W kg(−)(1)muscle mass) during ascending flight. This increase in power was achieved principally via an increase in muscle strain (29 % versus 36 %), rather than an increase in peak force (107 N versus 113 N) or cycle frequency (8.4 Hz versus 8.9 Hz). Body-mass-specific power output of mallards during slow level flight (17.0 W kg(−)(1)), measured in terms of pectoralis mechanical power, was similar to that measured recently in pigeons (16.1 W kg(−)(1)). Mallards compensate for their greater body mass and proportionately smaller wing area and pectoralis muscle volume by operating with a high myofibrillar stress to elevate mechanical power output.


1998 ◽  
Vol 201 (24) ◽  
pp. 3293-3307 ◽  
Author(s):  
A. A. Biewener ◽  
W. R. Corning ◽  
B. W. Tobalske

For the first time, we report in vivo measurements of pectoralis muscle length change obtained using sonomicrometry combined with measurements of its force development via deltopectoral crest strain recordings of a bird in free flight. These measurements allow us to characterize the contractile behavior and mechanical power output of the pectoralis under dynamic conditions of slow level flight in pigeons Columba livia. Our recordings confirm that the pigeon pectoralis generates in vivo work loops that begin with the rapid development of force as the muscle is being stretched or remains nearly isometric near the end of the upstroke. The pectoralis then shortens by a total of 32 % of its resting length during the downstroke,generating an average of 10.33.6 J kg-1 muscle (mean s.d.) of work per cycle for the anterior and posterior sites recorded among the five animals. In contrast to previous kinematic estimates of muscle length change relative to force development, the sonomicrometry measurements of fascicle length change show that force declines during muscle shortening. Simultaneous measurements of fascicle length change at anterior and posterior sites within the same muscle show significant (P<0.001, three of four animals) differences in fractional length (strain) change that averaged 1912 %, despite exhibiting similar work loop shape. Length changes at both anterior and posterior sites were nearly synchronous and had an asymmetrical pattern, with shortening occupying 63 % of the cycle. This nearly 2:1 phase ratio of shortening to lengthening probably favors the ability of the muscle to do work. Mean muscle shortening velocity was 5.381.33 and 4.881.27 lengths s-1 at the anterior and posterior sites respectively. Length excursions of the muscle were more variable at the end of the downstroke (maximum shortening), particularly when the birds landed,compared with highly uniform length excursions at the end of the upstroke(maximum lengthening). When averaged for the muscle as a whole, our in vivo work measurements yield a mass-specific net mechanical power output of 70. 2 W kg-1 for the muscle when the birds flew at 5-6 m s-1, with a wingbeat frequency of 8.7 Hz. This is 38 % greater than the value that we obtained previously for wild-type pigeons, but still 24-50 % less than that predicted by theory.


2001 ◽  
Vol 204 (21) ◽  
pp. 3587-3600 ◽  
Author(s):  
Graham N. Askew ◽  
Richard L. Marsh

SUMMARYSonomicrometry and electromyographic (EMG) recordings were made for the pectoralis muscle of blue-breasted quail (Coturnix chinensis) during take-off and horizontal flight. In both modes of flight, the pectoralis strain trajectory was asymmetrical, with 70 % of the total cycle time spent shortening. EMG activity was found to start just before mid-upstroke and continued into the downstroke. The wingbeat frequency was 23 Hz, and the total strain was 23 % of the mean resting length.Bundles of fibres were dissected from the pectoralis and subjected in vitro to the in vivo length and activity patterns, whilst measuring force. The net power output was only 80 W kg–1 because of a large artefact in the force record during lengthening. For more realistic estimates of the pectoralis power output, we ignored the power absorbed by the muscle bundles during lengthening. The net power output during shortening averaged over the entire cycle was approximately 350 W kg–1, and in several preparations over 400 W kg–1. Sawtooth cycles were also examined for comparison with the simulation cycles, which were identical in all respects apart from the velocity profile. The power output during these cycles was found to be 14 % lower than during the in vivo strain trajectory. This difference was due to a higher velocity of stretch, which resulted in greater activation and higher power output throughout the later part of shortening, and the increase in shortening velocity towards the end of shortening, which facilitated deactivation.The muscle was found to operate at a mean length shorter than the plateau of the length/force relationship, which resulted in the isometric stress measured at the mean resting length being lower than is typically reported for striated muscle.


1998 ◽  
Vol 201 (10) ◽  
pp. 1505-1526 ◽  
Author(s):  
J M Wakeling ◽  
I A Johnston

Fast-starts associated with escape responses were filmed at the median habitat temperatures of six teleost fish: Notothenia coriiceps and Notothenia rossii (Antarctica), Myoxocephalus scorpius (North Sea), Scorpaena notata and Serranus cabrilla (Mediterranean) and Paracirrhites forsteri (Indo-West-Pacific Ocean). Methods are presented for estimating the spine positions for silhouettes of swimming fish. These methods were used to validate techniques for calculating kinematics and muscle dynamics during fast-starts. The starts from all species show common patterns, with waves of body curvature travelling from head to tail and increasing in amplitude. Cross-validation with sonomicrometry studies allowed gearing ratios between the red and white muscle to be calculated. Gearing ratios must decrease towards the tail with a corresponding change in muscle geometry, resulting in similar white muscle fibre strains in all the myotomes during the start. A work-loop technique was used to measure mean muscle power output at similar strain and shortening durations to those found in vivo. The fast Sc. notata myotomal fibres produced a mean muscle-mass-specific power of 142.7 W kg-1 at 20 degrees C. Velocity, acceleration and hydrodynamic power output increased both with the travelling rate of the wave of body curvature and with the habitat temperature. At all temperatures, the predicted mean muscle-mass-specific power outputs, as calculated from swimming sequences, were similar to the muscle power outputs measured from work-loop experiments.


2018 ◽  
Vol 8 (12) ◽  
pp. 2637 ◽  
Author(s):  
Pawel Ziolkowski ◽  
Knud Zabrocki ◽  
Eckhard Müller

Finite element model (FEM)-based simulations are conducted for the application of a thermoelectric generator (TEG) between the hot core stream and the cool bypass flow at the nozzle of an aviation turbofan engine. This work reports the resulting requirements on the TEG design with respect to applied thermoelectric (TE) element lengths and filling factors (F) of the TE modules in order to achieve a positive effect on the specific fuel consumption. Assuming a virtual optimized TE material and varying the convective heat transfer coefficients (HTC) between the nozzle surfaces and the gas flows, this work reports the achievable power output. System-level requirement on the gravimetric power density (>100 Wkg−1) can only be met for F ≤ 21%. When extrapolating TEG coverage to the full nozzle surface, the power output reaches 1.65 kW per engine. The assessment of further potential for power generation is demonstrated by a parametric study on F, convective HTC, and materials performance. This study confirms a feasible design range for TEG installation on the aircraft nozzle with a positive impact on the fuel consumption. This application translates into a reduction of operational costs, allowing for an economically efficient TEG-installation with respect to the cost-specific power output of modern thermoelectric materials.


Author(s):  
Ali S. Alsagri ◽  
Andrew Chiasson ◽  
Ahmad Aljabr

A thermodynamic analysis and optimization of four supercritical CO2 Brayton cycles were conducted in this study in order to improve calculation accuracy; the feasibility of the cycles; and compare the cycles’ design points. In particular, the overall thermal efficiency and the power output are the main targets in the optimization study. With respect to improving the accuracy of the analytical model, a computationally efficient technique using constant conductance (UA) to represent heat exchanger performances is executed. Four Brayton cycles involved in this compression analysis, simple recaptured, recompression, pre-compression, and split expansion. The four cycle configurations were thermodynamically modeled and optimized based on a genetic algorithm (GA) using an Engineering Equation Solver (EES) software. Results show that at any operating condition under 600 °C inlet turbine temperature, the recompression sCO2 Brayton cycle achieves the highest thermal efficiency. Also, the findings show that the simple recuperated cycle has the highest specific power output in spite of its simplicity.


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