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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If a <strong>model</strong> does not fit correctly after fixing <strong>the</strong> origin, it means that it<br />
is not adapted to describe growth in this case. The only good reason to<br />
avoid constraint is when time (t0), size (D0) or both are unknown at <strong>the</strong><br />
origin <strong>of</strong> <strong>the</strong> growth process. It is unfortunately common with data<br />
collected in <strong>the</strong> field (Ebert, 1973, 1980a), when it is not possible to<br />
estimate age accurately (Ebert, 1998; Russell & Meredith, 2000). In this<br />
case, only relative growth can be studied and <strong>the</strong> problem <strong>of</strong> origin is thus<br />
eliminated de facto. However, <strong>the</strong> <strong>model</strong> must be reworked to fit relative<br />
growth data.<br />
In <strong>the</strong> present case, we have <strong>the</strong> information necessary to characterize<br />
<strong>the</strong> whole size distribution at <strong>the</strong> origin because we worked in aquaria:<br />
metamorphosis was artificially induced (same t0 for all individuals, see<br />
Grosjean et al, 1998, see Part I), and we have measurements <strong>of</strong> initial sizes<br />
just after it (Grosjean et al, 1996, see Part III). However, by using actual<br />
distribution instead <strong>of</strong> approximating D0 by <strong>the</strong> mean value for all<br />
quantiles, this parameter cannot be eliminated from eq. 31. The <strong>model</strong> is<br />
still viable, and perhaps a little bit more accurate for small sizes (see<br />
pr<strong>of</strong>ile 1 in Fig. 34B). Yet, we preferred to keep <strong>the</strong> simplest <strong>model</strong> in <strong>the</strong><br />
present case.<br />
At <strong>the</strong> o<strong>the</strong>r extreme <strong>of</strong> <strong>the</strong> growth process, a single parameter<br />
characterizes its completion when growth is asymptotic in all <strong>model</strong>s. It is<br />
parameter a in <strong>model</strong>s <strong>of</strong> Table 12 and ∆D∞ in eqs. 29, 31 and 35. Several<br />
authors questioned whe<strong>the</strong>r asymptotic growth is a biological reality, or<br />
just a ma<strong>the</strong>matical artifact. Ricker (1979) wrote a section untitled<br />
"asymptotic growth: is it real?" in a chapter <strong>of</strong> a book; Knight (1968)<br />
devoted a whole article to demonstrate it is a biological non-sense. Some<br />
<strong>model</strong>s with infinite growth appeared (for instance, Tanaka 1982, 1988).<br />
They were also tested on <strong>sea</strong> <strong>urchin</strong>s (Ebert, 1998, 1999; Ebert & Russell,<br />
1993). Some P. lividus were <strong>reared</strong> in our installations for 15 years. They<br />
reached <strong>the</strong>ir maximum size at 4 to 5 years old. They thus kept exactly <strong>the</strong><br />
same size for more than 10 years, proving asymptotic growth is a fact for<br />
Part IV: A growth <strong>model</strong> with intraspecific competition<br />
169