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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this species. For o<strong>the</strong>r species, where no plateau is observed, lifetime could<br />
be simply too short to reach it. Yet, it is <strong>the</strong>n impossible to tell if growth is<br />
determinate or indeterminate. Anyway, if maximum size is not actually<br />
reached, it is very difficult to estimate <strong>the</strong> corresponding parameter in <strong>the</strong><br />
<strong>model</strong>.<br />
We constrained ∆D∞ to be normally distributed in <strong>the</strong> envelope <strong>model</strong><br />
(eq. 35). It is in agreement with <strong>the</strong> analysis <strong>of</strong> size distributions for fullgrown<br />
animals (Grosjean et al, 1996, see Part III; current dataset). It is also<br />
a consequence <strong>of</strong> <strong>the</strong> genetic homogeneity <strong>of</strong> <strong>the</strong> batch as all individuals<br />
are issued from a single artificial fertilization, i.e., from one male and one<br />
female. In case where D0 is also considered as normally distributed, <strong>the</strong><br />
<strong>model</strong> relates individuals with largest D0 with individuals with largest<br />
∆D∞. But remember <strong>the</strong>se are virtual individuals. This could be <strong>the</strong> case<br />
for real echinoids or not. We cannot verify it without tagging individuals to<br />
track <strong>the</strong>m through time in <strong>the</strong> cohort.<br />
As a consequence <strong>of</strong> fixing k1 (eq. 33), ∆D∞ is <strong>the</strong> only parameter to<br />
contain information on relative growth potential <strong>of</strong> <strong>the</strong> individuals among<br />
<strong>the</strong> cohort in eq. 35. The kinetic parameter k1 could be viewed as<br />
environment-dependent (temperature, food, water quality, etc…). Since<br />
<strong>the</strong>se are <strong>the</strong> same for all animals because <strong>the</strong>y are in <strong>the</strong> same aquarium,<br />
<strong>the</strong>y are fed ad libitum and have access to <strong>the</strong> food <strong>the</strong> same way, it<br />
appears logical to fix k1. Fixing k2 is motivated by a similar reason: we<br />
want it to express one global aspect <strong>of</strong> <strong>the</strong> inhibition. When homogeneous<br />
batches <strong>of</strong> animals <strong>of</strong> same age and same genetic origin are <strong>reared</strong><br />
toge<strong>the</strong>r, speed at which inhibition is released is supposed to be about <strong>the</strong><br />
same for all individuals. This way, only l quantifies changes between<br />
virtual individuals (inhibitors versus inhibited). Of course, many o<strong>the</strong>r<br />
variants are possible, but at <strong>the</strong> cost <strong>of</strong> an increasing complexity <strong>of</strong> <strong>the</strong><br />
<strong>model</strong>.<br />
Indeed, as discussed by Grosjean et al (1996, see Part III), water<br />
quality is not exactly <strong>the</strong> same for all echinoids in culture because <strong>the</strong>y<br />
Part IV: A growth <strong>model</strong> with intraspecific competition<br />
170