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waders and their estuarine food supplies - Vlaams Instituut voor de ...

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frequency in diet (%)<br />

Fig. 2. Frequency distribution 0' I ot the selected <strong>de</strong>pth classes in<br />

Ihe Oy stercatchei's diet I'rcy on olTcr were distributed equally over<br />

III <strong>de</strong>pth classes. Combined data ol all experiments weic used In =<br />

305).<br />

dling time (Spearman rank correlation: p > 0.05). A<br />

significant increase (p < 0.05) occurred twice <strong>and</strong> a<br />

significant <strong>de</strong>crease (p < 0.05) once. In the 12 sessions<br />

where the bird took 10 prey <strong>and</strong> searching time per<br />

prey item was measured, there were no significant<br />

trends m searching time (p > 0.05) during the session.<br />

After each session we checked the opened bivalves<br />

for remaining llesh. but fortunately our bird never performed<br />

partial predation,<br />

Determining the effective touch area<br />

In or<strong>de</strong>r to calculate the probability that a buried prey<br />

would be ltx'ated by a r<strong>and</strong>omly searching Oystercatcher,<br />

we nee<strong>de</strong>d to know the cross-sectional area<br />

(touch area) of the bivalve <strong>and</strong> of the bill tip. We measured<br />

the touch area of 47 specimens (range 33-46<br />

mm) by pressing the bivalve vertically into mo<strong>de</strong>lling<br />

clay <strong>and</strong> measuring the impress of Ihe largest cross<br />

seeiion which, for our prey size (35-36 mm), was I cm<br />

below the top of the bivalve. The touch area was 0.22<br />

± 0.01 (mean ± SE) x shell length squared. We used<br />

Hulscher's (1982) value of bill lip touch area. The effective<br />

touch area was calculated as <strong>de</strong>scribed by<br />

Hulscher (1982). I he mean value for our prey size was<br />

6.15 cm 2 .<br />

The film sessions<br />

For a quantification of the duration <strong>and</strong> the <strong>de</strong>pth of the<br />

OPTIMAL FORAGING AND THE FUNCTIONAL RESPONSE<br />

142<br />

probes, we filmed the bird in five 3 min sessions w ith<br />

intervals of 5 min between. A 16-mm camera was<br />

used, with a speed of 16 frames per s.<br />

Analysis<br />

SPSS (Nie etal. 1975) was used for all stalistical analyses.<br />

Results<br />

Depth selection<br />

Prey out of the reach of the bird's bill (7 cm) were<br />

never taken (Fig. 2). So prey <strong>de</strong>nsity was <strong>de</strong>fined as the<br />

prey number present in the <strong>de</strong>pth classes 0-7 cm.<br />

Though prey were distributed equally over the <strong>de</strong>pth<br />

classes, the <strong>de</strong>eper prey were taken less than the shallow<br />

prey (Fig. 2).<br />

H<strong>and</strong>ling time<br />

H<strong>and</strong>ling time increased with prey <strong>de</strong>pth (Fig. 3). so<br />

prey profitability <strong>de</strong>creased with <strong>de</strong>pth.<br />

The analysis of the different components of han-<br />

UNLIFTED LIFTED<br />

jilting<br />

•""•(ea'ing<br />

H cutting<br />

2-3 4-5 6-7 0-1 2-3 4-5 6-7<br />

prey <strong>de</strong>pth (cm)<br />

HR. 3. Duration of h<strong>and</strong>ling componenls (mean cutting, eating <strong>and</strong><br />

lifting time ± SE) as a function of prey <strong>de</strong>plh. for A. Unlifted. <strong>and</strong> B.<br />

Lifted bivalves The distinguished components are: cutting (dark).<br />

ealing (grey I <strong>and</strong> Idling I light i. See Table I for si.iiisiical analysis.

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