scholarly journals Kinematics Measurement and Power Requirements of Fruitflies at Various Flight Speeds

Energies ◽  
2020 ◽  
Vol 13 (16) ◽  
pp. 4271
Author(s):  
Hao Jie Zhu ◽  
Mao Sun

Energy expenditure is a critical characteristic in evaluating the flight performance of flying insects. To investigate how the energy cost of small-sized insects varies with flight speed, we measured the detailed wing and body kinematics in the full speed range of fruitflies and computed the aerodynamic forces and power requirements of the flies. As flight speed increases, the body angle decreases and the stroke plane angle increases; the wingbeat frequency only changes slightly; the geometrical angle of attack in the middle upstroke increases; the stroke amplitude first decreases and then increases. The mechanical power of the fruitflies at all flight speeds is dominated by aerodynamic power (inertial power is very small), and the magnitude of aerodynamic power in upstroke increases significantly at high flight speeds due to the increase of the drag and the flapping velocity of the wing. The specific power (power required for flight divided by insect weigh) changes little when the advance ratio is below about 0.45 and afterwards increases sharply. That is, the specific power varies with flight speed according to a J-shaped curve, unlike those of aircrafts, birds and large-sized insects which vary with flight speed according to a U-shaped curve.

2014 ◽  
Vol 11 (98) ◽  
pp. 20140505 ◽  
Author(s):  
Erica J. Kim ◽  
Marta Wolf ◽  
Victor Manuel Ortega-Jimenez ◽  
Stanley H. Cheng ◽  
Robert Dudley

Aerodynamic performance and energetic savings for flight in ground effect are theoretically maximized during hovering, but have never been directly measured for flying animals. We evaluated flight kinematics, metabolic rates and induced flow velocities for Anna's hummingbirds hovering at heights (relative to wing length R = 5.5 cm) of 0.7 R , 0.9 R , 1.1 R , 1.7 R , 2.2 R and 8 R above a solid surface. Flight at heights less than or equal to 1.1 R resulted in significant reductions in the body angle, tail angle, anatomical stroke plane angle, wake-induced velocity, and mechanical and metabolic power expenditures when compared with flight at the control height of 8 R . By contrast, stroke plane angle relative to horizontal, wingbeat amplitude and wingbeat frequency were unexpectedly independent of height from ground. Qualitative smoke visualizations suggest that each wing generates a vortex ring during both down- and upstroke. These rings expand upon reaching the ground and present a complex turbulent interaction below the bird's body. Nonetheless, hovering near surfaces results in substantial energetic benefits for hummingbirds, and by inference for all volant taxa that either feed at flowers or otherwise fly close to plant or other surfaces.


2002 ◽  
Vol 205 (17) ◽  
pp. 2615-2626 ◽  
Author(s):  
R. D. Bullen ◽  
N. L. McKenzie

SUMMARYWingbeat frequency (fw) and amplitude(θw) were measured for 23 species of Australian bat,representing two sub-orders and six families. Maximum values were between 4 and 13 Hz for fw, and between 90 and 150° forθ w, depending on the species. Wingbeat frequency for each species was found to vary only slightly with flight speed over the lower half of the speed range. At high speeds, frequency is almost independent of velocity. Wingbeat frequency (Hz) depends on bat mass (m, kg) and flight speed (V, ms-1) according to the equation: fw=5.54-3.068log10m-2.857log10V. This simple relationship applies to both sub-orders and to all six families of bats studied. For 21 of the 23 species, the empirical values were within 1 Hz of the model values. One species, a small molossid, also had a second mode of flight in which fw was up to 3 Hz lower for all flight speeds.The following relationship predicts wingbeat amplitude to within±15° from flight speed and wing area (SREF,m2) at all flight speeds:θ w=56.92+5.18V+16.06log10SREF. This equation is based on data up to and including speeds that require maximum wingbeat amplitude to be sustained. For most species, the maximum wingbeat amplitude was 140°.


2012 ◽  
Vol 9 (77) ◽  
pp. 3260-3267 ◽  
Author(s):  
V. Medici ◽  
S. N. Fry

Fruitflies regulate flight speed by adjusting their body angle. To understand how low-level posture control serves an overall linear visual speed control strategy, we visually induced free-flight acceleration responses in a wind tunnel and measured the body kinematics using high-speed videography. Subsequently, we reverse engineered the transfer function mapping body pitch angle onto flight speed. A linear model is able to reproduce the behavioural data with good accuracy. Our results show that linearity in speed control is realized already at the level of body posture-mediated speed control and is therefore embodied at the level of the complex aerodynamic mechanisms of body and wings. Together with previous results, this study reveals the existence of a linear hierarchical control strategy, which can provide relevant control principles for biomimetic implementations, such as autonomous flying micro air vehicles.


2017 ◽  
Vol 7 (1) ◽  
pp. 20160086 ◽  
Author(s):  
J. D. Crall ◽  
J. J. Chang ◽  
R. L. Oppenheimer ◽  
S. A. Combes

Natural environments are characterized by variable wind that can pose significant challenges for flying animals and robots. However, our understanding of the flow conditions that animals experience outdoors and how these impact flight performance remains limited. Here, we combine laboratory and field experiments to characterize wind conditions encountered by foraging bumblebees in outdoor environments and test the effects of these conditions on flight. We used radio-frequency tags to track foraging activity of uniquely identified bumblebee ( Bombus impatiens ) workers, while simultaneously recording local wind flows. Despite being subjected to a wide range of speeds and turbulence intensities, we find that bees do not avoid foraging in windy conditions. We then examined the impacts of turbulence on bumblebee flight in a wind tunnel. Rolling instabilities increased in turbulence, but only at higher wind speeds. Bees displayed higher mean wingbeat frequency and stroke amplitude in these conditions, as well as increased asymmetry in stroke amplitude—suggesting that bees employ an array of active responses to enable flight in turbulence, which may increase the energetic cost of flight. Our results provide the first direct evidence that moderate, environmentally relevant turbulence affects insect flight performance, and suggest that flying insects use diverse mechanisms to cope with these instabilities.


2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Chengxiang Zhu ◽  
Xu Zhang ◽  
Fan Kong ◽  
Yancheng You

The operation of a propulsion system in terms of horizontal takeoff/landing and full-speed range serves as one of the main difficulties for hypersonic travelling. In the present work, a three-dimensional inward-turning inlet with tri-ducts for combined cycle engines is designed for the operation of three different modes controlled by a single rotational flap on the compression side, which efficiently simplifies the inlet structure and the flap control mechanism. At high flight speed between Mach 4 and 6, the pure scramjet mode is switched on, whereas both the ejector and the scramjet paths are open for a moderate Mach number between 2 and 4 with a larger throat area guaranteeing the inlet startability. In the low flight speed range with Mach number below 2, the additional turbojet path will be turned on to supply air for the turbine engine, whereas the other two paths remain open for spillage. Numerical simulations under different operation modes have proven the feasibility and good performance of the designed inlet, e.g., a nearly full mass flow ratio and a total pressure recovery around 0.5 can be achieved at the cruise speed. Meanwhile, the inlet works properly at low flight speeds which overcomes the typical starting problem of similar inlet designs. In the near future, wind tunnel experiments will be carried out to validate our inlet design and its performance.


2000 ◽  
Vol 203 (18) ◽  
pp. 2723-2735 ◽  
Author(s):  
H. Fischer ◽  
W. Kutsch

Little information is available about how the adult locust flight system manages to match the aerodynamic demands that result from an increase in body mass during postmoult maturation. In Schistocerca gregaria of both sexes, flight variables, including flight speed, ascent angle and body angle, were investigated under closed-loop conditions (i.e. during free flight) as a function of adult maturation. Motor patterns were examined by telemetric electromyography in juvenile and adult mature animals of both sexes. Functional relationships between particular flight variables were investigated by additional loading of the animals and by reductions in wing area. The results indicate that an increase in flight speed as the flight system matures enables it to match the aerodynamic demands resulting from increases in body mass. Furthermore, the data suggest that this postmoult increase in flight speed is not simply a consequence of the increase in wingbeat frequency observed during maturation. The instantaneous body angle during flight is controlled mainly by aerodynamic output from the wings. In addition, the mean body angle decreases during maturation in both sexes, and this may play an important part in the directional control of the resultant flight force vector.


2009 ◽  
Vol 276 (1664) ◽  
pp. 2109-2115 ◽  
Author(s):  
Christopher James Clark ◽  
Robert Dudley

The elongated tails adorning many male birds have traditionally been thought to degrade flight performance by increasing body drag. However, aerodynamic interactions between the body and tail can be substantial in some contexts, and a short tail may actually reduce rather than increase overall drag. To test how tail length affects flight performance, we manipulated the tails of Anna's hummingbirds ( Calypte anna ) by increasing their length with the greatly elongated tail streamers of the red-billed streamertail ( Trochilus polytmus ) and reducing their length by removing first the rectrices and then the entire tail (i.e. all rectrices and tail covert feathers). Flight performance was measured in a wind tunnel by measuring (i) the maximum forward speed at which the birds could fly and (ii) the metabolic cost of flight while flying at airspeeds from 0 to 14 m s −1 . We found a significant interaction effect between tail treatment and airspeed: an elongated tail increased the metabolic cost of flight by up to 11 per cent, and this effect was strongest at higher flight speeds. Maximum flight speed was concomitantly reduced by 3.4 per cent. Also, removing the entire tail decreased maximum flight speed by 2 per cent, suggesting beneficial aerodynamic effects for tails of normal length. The effects of elongation are thus subtle and airspeed-specific, suggesting that diversity in avian tail morphology is associated with only modest flight costs.


1991 ◽  
Vol 160 (1) ◽  
pp. 71-91 ◽  
Author(s):  
C. P. ELLINGTON

Flight performance seems to change systematically with body size: small animals can hover and fly over a wide range of speeds, but large birds taxi for takeoff and then fly over a narrow speed range. The traditional explanation for this is that the mass-specific power required for flight varies with speed according to a U-shaped curve, and it also scales between m0 and m1/6, where m is body mass. The mass-specific power available from the flight muscles is assumed to scale as m−1/3. As available power decreases with increasing body size, the range of attainable flight speeds becomes progressively reduced until the largest animals can only fly in the trough of the U-shaped curve. Above a particular size, the available power is insufficient and flapping flight is not possible. The underlying assumptions of this argument are examined in this review. Metabolic measurements are more consistent with a J-shaped curve, with little change in power from hovering to intermediate flight speeds, than with a U-shaped curve. Scaling of the mass-specific power required to fly agrees with predictions. The mass-specific power available from, the muscles, estimated from maximal loading studies, varies as m0.13. This scaling cannot be distinguished from that of the power required to fly, refuting the argument that power imposes an intrinsic scaling on flight performance. It is suggested instead that limitations on low-speed performance result from an adverse scaling of lift production with increasing body size.


1990 ◽  
Vol 150 (1) ◽  
pp. 37-53 ◽  
Author(s):  
ROBERT DUDLEY

Wing and body kinematics of free cruising flight are described for 37 species of Panamanian butterflies ranging over two orders of magnitude in body mass. Butterflies exhibit considerable diversity in body and wing shape, but morphological design is, in general, isometric. Wing loading and mean body diameter show positive allometry. The cruising flight of butterflies is characterized by low wingbeat frequencies (here averaging 11 Hz), stroke amplitudes averaging 103°, and forward speeds in excess of 1m s−1. Body angles during flight are close to horizontal, and stroke plane angles are correspondingly high. Advance ratios are typically greater than 0.9, indicating that the forward and flapping velocity vectors are of comparable magnitude. Flight speed scales with morphological parameters in general accordance with predictions based on isometric design. Interspecifically, no consistent correlation exists between wing kinematics and absolute flight speed. However, maximum positional angle and stroke amplitude tend to increase while body angle decreases with increased relative flight speed.


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