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Geology topics

C.J. Pennycuick

Publications and source records attributed to C.J. Pennycuick.

8 recordsLinked to original sources

Falcon versus grouse: flight adaptations of a predator and its prey

Several falcons were trained to fly along a 500 m course to a lure. The air speeds of the more consistent performers averaged about 1.5 times their calculated minimum power speeds, and occasionally reached 2.1 times the minimum power speed. Wing beat frequencies of all the falcons were above those estimated from earlier field observations, and the same was true of wild Sage Grouse Centrocercus urophasianus, a regular falconer's quarry in the study area. Measurements of grouse killed by falcons showed that their wings were short, with broad slotted tips, whereas the falcons' wings were longer in relation to their body mass, and tapered. The short wings of grouse result in fast flight, high power requirements, and reduced capacity for aerobic flight. Calculations indicated that the grouse should fly faster than the falcons, and had the large amount of flight muscle needed to do so, but that the falcons would be capable of prolonged aerobic flight, whereas the grouse probably would not. We surmise that Sage Grouse cannot fly continuously without incurring an oxygen debt, and are therefore not long-distance migrants, although this limitation is partly due to their large size, and would not apply to smaller galliform birds such as ptarmigan Lagopus spp. The wing action seen in video recordings of the falcons was not consistent with the maintenance of constant circulation. We call it 'chase mode' because it appears to be associated with a high level of muscular exertion, without special regard to fuel economy. It shows features in common with the 'bounding' flight of passerines.

Journal of Avian Biology

Fifty-fifth Christmas Bird Count. 159. Ocean City, Md

The distribution of dynamic pressure behind a Harris' hawk's wing was sampled using a wake rake consisting of 15 pitot tubes and one static tube. The hawk was holding on to a perch, but at an air speed and gliding angle at which it was capable of gliding. The perch was instrumented, so that the lift developed by the wing was known and the lift coefficient could be calculated. The mean of 92 estimates of profile drag coefficient was 0.0207, with standard deviation 0.0079. Lift coefficients ranged from 0.51 to 1.08. Reynolds numbers were nearly all in the range 143000-194000. The estimates of profile drag coefficient were reconcilable with previous estimates of the wing profile drag of the same bird, obtained by the subtractive method, and also with values predicted by the `Airfoil-ii? program for designing aerofoils, based on a digitized wing profile from the ulnar region of the wing. The thickness of the wake suggested that the boundary layer was mostly or fully turbulent in most observations and separated in some, possibly as an active means of creating drag for control purposes. It appears that the bird could momentarily either increase or decrease the profile drag of specific parts of the wing, by active changes of shape, and it appeared to use the carpo-metacarpal region especially for such control movements. Further investigation in a low turbulence wind tunnel would help to resolve doubts about the possible influence of airstream turbulence on the behaviour of the boundary layer.

Journal of Experimental Biology

Foraging flights of the white-tailed tropicbird (Phaethon lepturus): Radiotracking and doubly-labelled water

Radiotracking transmitters were fitted to White-tailed Tropicbirds nesting at Culebra, Puerto Rico. Foragers were located by light aircraft out to 89 km SSW of the nesting colony, over a deep-water foraging area south of Vieques Island, Puerto Rico and west of St Croix, U. S. Virgin Islands. Two birds were followed out to 176 km NNW from the colony, over the Puerto Rico Trench, but these did not subsequently return. Foragers carrying radio transmitters performed similarly to those without, in terms of duration of absence from the colony, and mass of food brought for the chick. However, measuremetns of energy consumption by the doubly labelled water method indicated that birds with transmitters consumed significantly more energy than those without.

Colonial Waterbirds

Climbing performance of Harris' hawks (Parabuteo unicinctus) with added load: Implications for muscle mechanics and for radiotracking

Two Harris’ hawks were trained to fly along horizontal and climbing flight paths, while carrying loads of various masses, to provide data for estimating available muscle power during short flights. The body mass of both hawks was about 920g, and they were able to carry loads up to 630 g in horizontal flight. The rate of climb decreased with increasing all-up mass, as also did the climbing power (product of weight and rate of climb). Various assumptions about the aerodynamic power in low-speed climbs led to estimates of the maximum power output of the flight muscles ranging from 41 to 46 W. This, in turn, would imply a stress during shortening of around 210 kPa. The effects of a radio package on a bird that is raising young should be considered in relation to the food load that the forager can normally carry, rather than in relation to its body mass.

Journal of Experimental Biology

Aerial tracking of radio-marked white-tailed tropicbirds over the Caribbean Sea

We radio-marked nesting white-tailed tropicbirds at Culebra National Wildlife Refuge, Puerto Rico, and tracked them from a Cessna 182 during flights over the open sea. Locations of the birds were determined using standard aerial telemetry techniques for side-facing Yagi antennas. We used strut-mounted, 4-element Yagi antennas connected to a switchbox and scanning receiver. By recording bearing and distance from at least 1 of 3 aeronautical navigation beacons, the position of the aircraft and the bird could be estimated with an error of about 2 km. On several occasions we plotted the general heading of a bird and then relocated and tracked the same bird on the following day. Our method of aerial tracking and navigation was useful for tracking birds over the sea to at least 116 km from the breeding colony

Book chapter

Empirical estimates of body drag of large waterfowl and raptors

Measurements of the body frontal area of some large living waterfowl (Anatidae) and raptors (Falconiformes) were found to vary with the two-thirds power of the body mass, with no distinction between the two groups. Wind tunnel measurements on frozen bodies gave drag coefficients ranging from 0·25 to 0·39, in the Reynolds number range 145 000 to 462000. Combining these observations with those of Prior (1984) , which extended to lower Reynolds numbers, a practical rule is proposed for choosing a value of the body drag coefficient for use in performance estimates.

Journal of Experimental Biology

Wind tunnel experiments to assess the effect of back-mounted radio transmitters on bird body drag

The aerodynamic drag of bird bodies was measured in a wind tunnel, with and without back-mounted dummy radio transmitters. Flight performance estimates indicate that the drag of a large transmitter can cause a substantial reduction of a migrant’s range, that is, the distance it can cover in non-stop flight. The drag of the transmitter can be reduced by arranging the components in an elongated shape, so minimizing the frontal area. The addition of a rounded fairing to the front end, and a pointed fairing behind, was found to reduce the drag of the transmitter by about one-third, as compared with an unfaired rectangular box.

Journal of Experimental Biology