The Energetics of Hovering in the Mandarin Fish (Synchropus Picturatus)

1979 ◽  
Vol 82 (1) ◽  
pp. 25-33 ◽  
Author(s):  
R. W. BLAKE

The influence of the ground effect on the energetics of hovering in Synchropus picturatus Peters, a negatively buoyant, demersal teleost was studied. Changes in pectoral fin kinematics, the ultimate water velocity in the wake below the fins, the calculated minimum induced thrust and power required to hover are related to the height at which the animal hovers above the substrate. The profile power required to overcome the frictional drag on the fins has been calculated for the case of both a laminar and a turbulent boundary layer over the fins. Reductions in the total power needed to hover (as compared with that required out of ground effect) of 30–60% have been calculated for Synchropus when hovering at commonly observed heights above the bottom. Results are discussed in relation to the hovering flight of birds, insects and helicopters.

2017 ◽  
Vol 29 (6) ◽  
pp. 065103 ◽  
Author(s):  
Joon-Seok Kim ◽  
Jinyul Hwang ◽  
Min Yoon ◽  
Junsun Ahn ◽  
Hyung Jin Sung

2017 ◽  
Vol 139 (10) ◽  
Author(s):  
Luke S. Roberts ◽  
Mark V. Finnis ◽  
Kevin Knowles

The transition from a laminar to turbulent boundary layer on a wing operating at low Reynolds numbers can have a large effect on its aerodynamic performance. For a wing operating in ground effect, where very low pressures and large pressure gradients are common, the effect is even greater. A study was conducted into the effect of forcing boundary-layer transition on the suction surface of an inverted GA(W)-1 section single-element wing in ground effect, which is representative of a racing-car front wing. Transition to a turbulent boundary layer was forced at varying chordwise locations and compared to the free-transition case using experimental and computational methods. Forcing transition caused the laminar-separation bubble, which was the unforced transition mechanism, to be eliminated in all cases and trailing-edge separation to occur instead. The aerodynamic forces produced by the wing with trailing-edge separation were shown to be dependent on trip location. As the trip was moved upstream the separation point also moved upstream, this led to an increase in drag and reduction in downforce. In addition to significant changes to the pressure field around the wing, turbulent energy in the wake was considerably reduced by forcing transition. The differences between free- and forced-transition wings were shown to be significant, highlighting the importance of modeling transition for ground-effect wings. Additionally, it has been shown that while it is possible to reproduce the force coefficient of a higher Reynolds-number case by forcing the boundary layer to a turbulent state, the flow features, both on-surface and off-surface, are not recreated.


1961 ◽  
Vol 38 (2) ◽  
pp. 365-390
Author(s):  
M. F. M. OSBORNE

The annual spawning migration of Pacific Coast salmon up the Columbia and Amur rivers has been analysed as an experiment on the maximum range of an unefuelled vehicle, since the fish do not eat during this migration. The fuel (primarily fat) available to real fish is compared to that computed for an equivalent rigid vehicle with the following performance specifications which may be regarded as optimum ones for marine vehicles. 1. A choice for the speed of ascent against the average river current corresponding to the least fuel consumption, without seeking systematically either low- or highvelocity water. 2. A drag coefficient corresponding to a turbulent boundary layer with no separation. 3. An overall efficiency of 24% for converting the heat of combustion of the fuel to directed kinetic energy in the wake. Under these assumptions, the vehicles usually require slightly more fuel than the corresponding fish which they are intended to approximate; in the case of blueback salmon, the vehicle requires about five times as much. One, therefore, concludes that the fish have a performance superior to that of the best engineered rigid vehicles, as defined and operated under the above three specifications. Suggested explanations for the apparently superior performance of the fish are: (1) a deliberate seeking, by the fish, of low-velocity water close to the bottom or shoreline; (2) the ability of the fish to maintain a laminar rather than turbulent boundary layer; (3) the ability of the fish to extract energy from the turbulent velocity fluctuationsof the river. Analysis of salmon counts over the Bonneville and Rock Island dams on the Columbia River shows that the average velocity of the fish upstream is influenced by the velocity of the water downstream in the following peculiar fashion, depending upon whether one considers water-velocity variations through the course of a year, or variations at a fixed season of the year, from one year to the next. The general effect of the water velocity as it varies through a year, is to slow the fish down when the water velocity is large (at the June flood peak) and to permit faster ascent when the water velocity is less, in both preceding and following months. But at a fixed season of the year, prior to the flood peak in June, relatively high-velocity water speeds the fish up. At a fixed season after the flood peak, relatively high-velocity water slows them down. These relationships are in agreement with other biological observations and with an analysis of navigation for minimum fuel consumption. Data and methods are given permitting a calculation of the average water velocity in the Columbia River, from the mouth to the headwaters, for any season of the year.


1958 ◽  
Vol 62 (566) ◽  
pp. 135-138
Author(s):  
Henry Barrow

For a Flat Surface at zero incidence in a deep uniform stream, the total frictional drag F per unit width of the surface can be calculated from the well known equationUsing the momentum principle in the usual way, it can be shown that when fluid is added locally to the flow through the surface, the total frictional drag F1 is given by


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