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Growth model of the reared sea urchin Paracentrotus ... - SciViews

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lividus. 10 to 15% <strong>of</strong> <strong>the</strong> largest individuals (<strong>the</strong> inhibitors) in <strong>the</strong><br />

populations grow at <strong>the</strong>ir maximal speed (i.e. <strong>the</strong> growth speed <strong>the</strong>y would<br />

have if <strong>the</strong>y were alone in <strong>the</strong> same food and environmental conditions).<br />

The growth <strong>of</strong> o<strong>the</strong>rs depends upon <strong>the</strong>ir relative size in <strong>the</strong> population<br />

(<strong>the</strong> smaller <strong>the</strong>y are, <strong>the</strong> slower <strong>the</strong>y grow). The cause <strong>of</strong> this inhibition is<br />

not known yet, but it does not seem to be food-related: in <strong>the</strong> experiments,<br />

all individuals had access to food ad libitum. Inhibition progressively fades<br />

out when larger individuals reach <strong>the</strong>ir asymptotic size and are caught up<br />

with smaller ones that are still growing.<br />

According to <strong>the</strong>se observations, a semantic formulation <strong>of</strong> <strong>the</strong><br />

problem becomes: "a young, small individual is potentially inhibited in its<br />

growth, but gradually reaches its maximum size with age". It can also be<br />

represented by two sets and one transition, but now <strong>the</strong> S set is <strong>the</strong> minimal<br />

size with time (with maximum inhibition) and L set is <strong>the</strong> size at <strong>the</strong> age<br />

where <strong>the</strong> growth speed is maximal (with no inhibition at all). The<br />

transition is now <strong>the</strong> expression <strong>of</strong> a progressive release <strong>of</strong> <strong>the</strong> inhibition,<br />

instead <strong>of</strong> a representation <strong>of</strong> <strong>the</strong> entire growth process. The difficulty<br />

resides in <strong>the</strong> proper characterization <strong>of</strong> sets and membership functions<br />

with age.<br />

First <strong>of</strong> all, we use a time-scale t' with a well-defined origin that really<br />

coincides with <strong>the</strong> initiation <strong>of</strong> <strong>the</strong> growth process. Until now, we used<br />

(time-scale t) <strong>the</strong> age <strong>of</strong> <strong>sea</strong> <strong>urchin</strong>s (since fertilization, thus including<br />

larval life). However, growth <strong>of</strong> postmetamorphic <strong>sea</strong> <strong>urchin</strong>s really starts<br />

after metamorphosis. Knowing <strong>the</strong> age at metamorphosis (t0), t' is simply:<br />

Part IV: A growth <strong>model</strong> with intraspecific competition<br />

t' = t − t0<br />

(23)<br />

For <strong>the</strong> studied dataset, metamorphosis was artificially induced for all<br />

echinoids in <strong>the</strong> batch at <strong>the</strong> same time at 30 days old. t' scale is thus<br />

shifted to <strong>the</strong> left by t0 = 30 days.<br />

Set S corresponds to <strong>the</strong> minimum possible growth, that is simply no<br />

growth at all. Thus, in set S, size remains constant at its minimum initial<br />

149

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