Aerodynamic Modelling of Insect Wings Using Joukowski Transformation

2021 ◽  
Author(s):  
Mostafa R. Nabawy ◽  
Gonzalo J. Villamor ◽  
Hao Li
1964 ◽  
Vol 96 (1-2) ◽  
pp. 98-98 ◽  
Author(s):  
J. W. Arnold

Despite their inert appearance, the wings of insects are living appendages and are supplied with blood. This is true for definitive wings as well as for developing ones, and for modified wings such as tegmina, elytra, hemelytra, and halteres as for those that are specialized for flight. Typically the blood circulates only through the wing veins, but in some insects it escapes into the surrounding membrane in certain areas, and in highly modified forms it may be entirely unconfined. The course of circulation is basically the same in the wings of most insects. It flows outward from the body in the costo-medial veins, moves toward the posterior margins via cross-veins, and returns to the body through the cubito-anal veins and axillary cord. However, rhe precise route followed is highly variable concomitant with distinctive patterns of venation in different taxonomic groups and with wing structure. This is illustrated for a number of orders.


2007 ◽  
Vol 75 ◽  
pp. 012011 ◽  
Author(s):  
Luca Greco ◽  
Claudio Testa ◽  
Francesco Salvatore

2008 ◽  
Vol 20 (20) ◽  
pp. 204142 ◽  
Author(s):  
S Sudo ◽  
K Tsuyuki ◽  
T Yano ◽  
K Takagi
Keyword(s):  

Water exchange between insects and their environment via the vapour phase includes influx and efflux components. The pressure cycle theory postulates that insects (and some other arthropods) can regulate the relative rates of influx and efflux of water vapour by modulating hydrostatic pressures at a vapour-liquid interface by compressing or expanding a sealed, gas-filled cavity. Some such cavities, like the tracheal system, could be compressed by elevated pressure in all or part of the haemocoele. Others, perhaps including the muscular rectum of flea prepupae, could be compressed by intrinsic muscles. Maddrell Insect Physiol . 8, 199 (1971)) suggested a pressure cycle mechanism of this kind to account for rectal uptake of water vapour in Thermobia but did not find it compatible with quantitative information then available. Newer evidence conforms better with the proposed mechanism. Cyclical pressure changes are of widespread occurrence in insects and have sometimes been shown to depend on water status. Evidence is reviewed for the role of the tracheal system as an avenue for net exchange of water between the insect and its environment. Because water and respiratory gases share common pathways, most published findings fail to distinguish between the conventional view that the tracheal system has evolved as a site for distribution and exchange of respiratory gases and that any water exchange occurring in it is generally incidental and nonadaptive, and the theory proposed here. The pressure cycle theory offers a supplementary explanation not incompatible with evidence so far available. The relative importance of water economy and respiratory exchange in the functioning of compressible cavities such as the tracheal system remains to be explored. Some further implications of the pressure cycle theory are discussed. Consideration is given to the possible involvement of vapour-phase transport in the internal redistribution of water within the body. It is suggested that some insect wings may constitute internal vapour-liquid exchange sites, where water can move from the body fluids to the intratracheal gas. Ambient and body temperature must influence rates of vapour-liquid mass transfer. If elevated body temperature promotes evaporative discharge of the metabolic water burden that has been shown to accumulate during flight in some large insects, their minimum threshold thoracic temperature for sustained flight may relate to the maintenance of water balance. The role of water economy in the early evolution of insect wings is considered. Pressure cycles might help to maintain water balance in surface-breathing insects living in fresh and saline waters, but the turbulence of the surface of the open sea might prevent truly marine forms from using this mechanism.


2018 ◽  
Vol 123 (1259) ◽  
pp. 79-92
Author(s):  
A. Kumar ◽  
A. K. Ghosh

ABSTRACTIn this paper, a Gaussian process regression (GPR)-based novel method is proposed for non-linear aerodynamic modelling of the aircraft using flight data. This data-driven regression approach uses the kernel-based probabilistic model to predict the non-linearity. The efficacy of this method is examined and validated by estimating force and moment coefficients using research aircraft flight data. Estimated coefficients of aerodynamic force and moment using GPR method are compared with the estimated coefficients using maximum-likelihood estimation (MLE) method. Estimated coefficients from the GPR method are statistically analysed and found to be at par with estimated coefficients from MLE, which is popularly used as a conventional method. GPR approach does not require to solve the complex equations of motion. GPR further can be directed for the generalised applications in the area of aeroelasticity, load estimation, and optimisation.


Author(s):  
Masaki Fuchiwaki ◽  
Kazuhiro Tanaka

A typical example of the flow field around a moving elastic body is that around butterfly wings. Butterflies fly by skillfully controlling this flow field, and vortices are generated around their bodies. The motion of their elastic wings produces dynamic fluid forces by manipulating the flow field. For this reason, there has been increased academic interest in the flow field and dynamic fluid forces produced by butterfly wings. A number of recent studies have qualitatively and quantitatively examined the flow field around insect wings. In some such previous studies, the vortex ring or vortex loop formed on the wing was visualized. However, the characteristics of dynamic forces generated by the flapping insect wing are not yet sufficiently understood. The purpose of the present study is to investigate the characteristics of dynamic lift and thrust produced by the flapping butterfly wing and the relationship between the dynamic lift and thrust and the flow field around the butterfly. We conducted the dynamic lift and thrust measurements of a fixed flapping butterfly, Idea leuconoe, using a six-axes sensor. Moreover, two-dimensional PIV measurement was conducted in the wake of the butterfly. The butterfly produced dynamic lift in downward flapping which became maximum at a flapping angle of approximately 0.0 deg. At the same time, the butterfly produced negative dynamic thrust during downward flapping. The negative dynamic thrust was not produced hydrodynamically by a flapping butterfly wing because a jet was not formed in front of the butterfly. The negative dynamic thrust was the kicking force for jumping and the maximum of this kicking force was about 6.0 times as large as the weight. On the other hand, the butterfly produced dynamic thrust in upward flapping which was approximately 6.0 times as large as the weight of the butterfly. However, the attacking force by the abdomen of the butterfly was included in the dynamic thrust and we have not yet clarified quantitatively the dynamic thrust produced by the butterfly wing.


1997 ◽  
Vol 50 (1) ◽  
pp. 13-24 ◽  
Author(s):  
Michael H. Dickinson ◽  
Susannah Hannaford ◽  
John Palka

2018 ◽  
Vol 115 (40) ◽  
pp. 9905-9910 ◽  
Author(s):  
Jordan Hoffmann ◽  
Seth Donoughe ◽  
Kathy Li ◽  
Mary K. Salcedo ◽  
Chris H. Rycroft

Insect wings are typically supported by thickened struts called veins. These veins form diverse geometric patterns across insects. For many insect species, even the left and right wings from the same individual have veins with unique topological arrangements, and little is known about how these patterns form. We present a large-scale quantitative study of the fingerprint-like “secondary veins.” We compile a dataset of wings from 232 species and 17 families from the order Odonata (dragonflies and damselflies), a group with particularly elaborate vein patterns. We characterize the geometric arrangements of veins and develop a simple model of secondary vein patterning. We show that our model is capable of recapitulating the vein geometries of species from other, distantly related winged insect clades.


Sign in / Sign up

Export Citation Format

Share Document