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RACING PIGEONS – IMPACT OF RAPTOR PREDATION

RACING PIGEONS – IMPACT OF RAPTOR PREDATION

RACING PIGEONS – IMPACT OF RAPTOR PREDATION

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development to ensure that the chemical is not only effective but also completely safe<br />

to pigeons and fanciers. Unfortunately, at its current state of development, and<br />

specifically in view of health, safety and legality issues, there are concerns over<br />

advocating this technique. A further problem with CTA is that a relatively large<br />

percentage of the potential prey would need to be treated in order to maximise the<br />

chances of predation of a treated individual.<br />

An alternative mode of application (aerosol spray) of methyl anthranilate as a bird<br />

repellent has been investigated in preliminary experiments (Stevens & Clarke 1998).<br />

In a test chamber, starlings exhibited behavioural responses indicating sensory<br />

irritation on exposure to a methyl anthranilate aerosol. Moreover, habituation was not<br />

apparent following repeated exposure to the aerosol. Potential applications postulated<br />

for such an aerosol repellent technique are the protection of birds through deterrence<br />

from hazardous waste sites and the dispersal of roosts to protect public health and<br />

safety.<br />

Supplementary (diversionary) feeding<br />

The provision of supplementary, diversionary or ‘buffer’ prey has been used in a<br />

number of circumstances in attempts to reduce raptor predation. The predation rate in<br />

a colony of little terns Sterna albifrons, in Norfolk, UK, decreased when the two pairs<br />

of resident kestrels Falco tinnunculus were provided with supplemental prey (dead<br />

mice) (Durdin 1993). Supplementary feeding of peregrines, however, had little<br />

success during attempts to protect a roseate tern Sterna dougallii colony (Avery &<br />

Winder 1990). At pheasant release pens, the provision of an alternative food source<br />

was suggested to be effective in reducing predation by sparrowhawks (Lloyd 1976)<br />

and buzzards Buteo buteo (Harradine et al. 1997). On grouse moors, the provision of<br />

supplementary food to hen harriers Circus cyaneus significantly reduced their<br />

predation on red grouse Lagopus scoticus chicks (Redpath et al., 2001). Hinsley &<br />

Redpath (1996) reported the establishment of pigeon lofts on grouse moors in<br />

attempts to protect grouse Lagopus lagopus from peregrines.<br />

There is, however, a potential danger in providing supplementary food, which is that<br />

in the long-term it may lead to an increase in predator-density, if prey availability is<br />

limiting predator numbers. In Sweden, goshawk range size was smaller and breeding<br />

density higher in areas rich in rabbits than elsewhere (Kenward 1982a). In one such<br />

area goshawk predation on wild pheasants Phasianus colchicus was particularly high<br />

(Kenward 1982b, 1986). It was suggested that the predation on pheasants was<br />

exacerbated by the abundance of rabbits drawing more hawks into the area than<br />

would normally have occurred in such a habitat. Conversely, in Langholm, Scotland,<br />

there was little evidence that providing supplementary food for hen harriers in spring<br />

increased breeding density (Redpath et al. 1999 cited in UK Raptor Working Group<br />

2000). For commercial fisheries it has been suggested that higher overall fish<br />

densities, due to stocking buffer prey alongside commercial species, may serve as an<br />

increased attraction to predators (Elson 1962, Draulans 1987). To avoid this, the<br />

provision of buffer prey at alternative sites away from important fisheries was<br />

suggested as a preferred option (Mott & Boyd 1995).<br />

With respect to raptor predation on racing pigeons supplementary feeding may be<br />

suitable for use during the limited period of peak attacks: sparrowhawks - March and<br />

April, peregrine - May and June. Carcasses from pest control operations by local<br />

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