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