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

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FEEDING RADIUS, BURYING DEPTH AND SIPHON SIZE<br />

2mg<br />

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I mg<br />

1 2 3 4 5 6 7<br />

siphon length (cm)<br />

Fig. 7. A. Weighl (mg AFDWi of ihe exten<strong>de</strong>d siphon. B. weight<br />

ot the exten<strong>de</strong>d siphon ling cm ') <strong>and</strong> C. weighl of the internal<br />

siphon ling AFDW) in Macoma 15 mm long as a function of the<br />

length of the exten<strong>de</strong>d siphon. The three regression lines in each<br />

panel refer to siphons with different total weights: number of cases<br />

given in the upper panel. The weighl of the exten<strong>de</strong>d siphon <strong>de</strong>pends<br />

on siphon length (R- = 0.281) <strong>and</strong> on total siphon weight<br />

(R 2 = 0.295); the interaction term was not significant<br />

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possible if more siphon tissue is protru<strong>de</strong>d, the weight<br />

ol the siphon remaining within the shell must be less<br />

when the siphon is stretched more, <strong>and</strong> this is exact I v<br />

what was found (Fig. 7C). When extending <strong>their</strong><br />

siphon, Macoma kept part of it 120 to 70'.;) within the<br />

shell. The size of this 'internal' part of the siphon <strong>de</strong>creased<br />

if the siphon was exten<strong>de</strong>d further <strong>and</strong> was<br />

small in Macoma of a low siphon weight.<br />

Discussion<br />

Relation between feeding radius <strong>and</strong> shell size<br />

As would be expected, there is a linear, rather than exponential,<br />

increase in average feeding radius with shell<br />

size (Figs. 1 <strong>and</strong> 2). If <strong>food</strong> is limiting <strong>and</strong> assuming<br />

lhai ihe proportion of the requirements taken Irom the<br />

surface, <strong>and</strong> the efficiency wilh which they are collected,<br />

is the same for the different si/e classes, the individual<br />

feeding area should be equivalent to the total<br />

<strong>food</strong> <strong>de</strong>m<strong>and</strong>s of a <strong>de</strong>posit-feeding bivalve. This<br />

means that the feeding radius should be a function of<br />

<strong>food</strong> intake" 5 . Other things being equal, energy requirements<br />

are a function of body weight" 7 \ found<br />

both in comparisons between species <strong>and</strong> within individual<br />

Scrobicularia of different flesh weights<br />

(Hughes 1970b). The ash-free dry weight of ihe flesh<br />

in Scrobicularia <strong>and</strong> Macoma is an allometric function<br />

of shell length, with the exponent of 2.9 (Zwarts 1991).<br />

The prediction therefore would be that feeding radius<br />

would be function of shell length with an exponent of<br />

0.5x0.75x2.9, or 1.09. <strong>and</strong> so close to observed linearity.<br />

Other studies found no. or hardly any. relationship<br />

between feeding radius <strong>and</strong> shell size (Wik<strong>and</strong>er 1980,<br />

Levinton 1991). This may indicate that larger individuals<br />

lake relatively more <strong>food</strong> from the overlying water,<br />

<strong>and</strong>/or are able to graze the surface more efficiently.<br />

On the other h<strong>and</strong>, the individual variation in<br />

feeding radius of animals of ihe same size is very large<br />

<strong>and</strong> this is associated with the huge variation in siphon<br />

weight (see below: Figs. 8B <strong>and</strong> 9C). Hence the relationship<br />

between average feeding radius <strong>and</strong> shell size<br />

can easily be overlooked if the sample size is small.<br />

Relation between siphon size <strong>and</strong> shell length<br />

The exponent of the allometric relationship between

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