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

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lahle- I. Numenius arquala. Search rate predicted bj ihe 'und<br />

method' i explanation in the text) compared io the search rate .is <strong>de</strong>rived<br />

from ihc product ot pace length (as measured Irom the prints<br />

in the muill anil pace frequency. All dala were collected for one<br />

Curlew observed an entire low water period<br />

Search rule<br />

Grid method icin s ')<br />

Pace rate x pace lengih (cm s ; i<br />

pace rate (pace s'')<br />

pace length (cm)<br />

VERSATILITY OF CURLEWS FEEDING ON NEREIS<br />

Mean ± SE »<br />

22.6*0.02 180<br />

22Ja<br />

1.8*0.02 63<br />

13.6 ±0.68 20<br />

length or size of colour ring as a reference), (4) duration<br />

of 4 types of activity io die nearest second: h<strong>and</strong>ling<br />

time (the Curlew catches <strong>and</strong> swallows a prey; if<br />

h<strong>and</strong>ling is prece<strong>de</strong>d by probing this is always a part of<br />

the h<strong>and</strong>ling lime): probing time ithe Curlew probes a<br />

greater part of iis bill into the substrate without finding<br />

a prey): searching time (feeding time without probing<br />

<strong>and</strong> h<strong>and</strong>ling: single pecks (duration < I s) are consi<strong>de</strong>red<br />

as part of the searching limci: non-feeding time<br />

(preening, resting <strong>and</strong> aggression, bin kleptoparasitism<br />

is consi<strong>de</strong>red as part of the feeding time).<br />

Additional information was collected for Cut lew s<br />

50<br />

4;;<br />

30<br />

ST 20<br />

10<br />

observer<br />

ABCD<br />

DDII<br />

- 4 - J 3 - 2 - 1 0 li JL<br />

1 2 3<br />

<strong>de</strong>viation from observer E (cm)<br />

Fig. 1. Comparison between observers who estimated lengths of<br />

Vi reis diversii aim- taken by a Curlew. Frequency distributions show<br />

agreement of 4 different observers t A: n = 32: B: n = 32: C: n • 56;<br />

D: n = 111 with 0*M H worms were *' lo |4cm.<br />

319<br />

feeding within the grid of 5x5 m plots around the<br />

hi<strong>de</strong>s, viz. the habitat from which the prey was taken<br />

(water film or dry surface) <strong>and</strong> coverage by water film<br />

(estimated horn the tower as '< of the surface in the<br />

5x5 mplot visited).<br />

All observations were pooled in 3 min periods. The<br />

analyses for this paper are confined to 3 min periods<br />

during which < 20% of the total biomass of prey taken<br />

by male Curlews (bill lengih < 12.5 mm) consisted of<br />

prey other lhan Nereis. After these 2 restrictions a total<br />

feeding time of 6335 min was left for analysis.<br />

The search rate was estimaied by measuring the<br />

pace frequency (time to make 50 Steps during searching)<br />

<strong>and</strong> pace length (from prints in the mud). The<br />

search rate of Curlews feeding within the grid of 5x5<br />

m plots could be estimated from the path length as predicted<br />

with the grid method (Reddingius et al. 1983).<br />

The path length equals the number of grid crossings<br />

multiplied by TC/4 times the si<strong>de</strong> lengih of the plots (in<br />

our case 5 m). On one day both methods of measuring<br />

search rate were used simultaneously <strong>and</strong> showed corresponding<br />

results (Table I).<br />

1 he estimation of worm size by most observers differed<br />

little: 39*3! ol the worms taken b) a Curlew were<br />

6 8 10 12 14<br />

estimated worm length (cm)<br />

Kig. 2. Nereis div, rskohtr Worm size measured in the laboratory<br />

i maximal length of creeping worms, see Hsselink & Zwarts 198<br />

a function of estimated worm size, averaged for 5 observers using a<br />

lelcseopc al a distance of I00 m. Worms were held near the bill of 2<br />

smiled Curlews iO: bill lengih 11.7 cm. n = 136 <strong>and</strong> •: 14.7 cm.<br />

n = 74).

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