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

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Constraining parameters as we did in eq. 30-34 leads to a double benefit.<br />

First, it simplifies <strong>the</strong> <strong>model</strong>. In <strong>the</strong> present case, we started with a 5parameter<br />

unconstrained classical <strong>model</strong> (eq. 29) and we ended with a 5parameter<br />

constrained envelope <strong>model</strong> (eq. 35). Yet, <strong>the</strong> latter contains<br />

much more information than <strong>the</strong> former. Second, if constraints are<br />

formulated according to some knowledge about <strong>the</strong> underlying<br />

phenomenon (value <strong>of</strong> <strong>the</strong> intercept corresponding to actual initial size) or<br />

to some reasonable hypo<strong>the</strong>ses (relation between l and τ, in regard with<br />

information in <strong>the</strong> literature), parameters remain meaningful in <strong>the</strong> fitted<br />

<strong>model</strong>. A correct formulation <strong>of</strong> both <strong>the</strong> initial unconstrained <strong>model</strong> and<br />

<strong>of</strong> superimposed constraints is a bit <strong>of</strong> an art. It requires many trials and<br />

errors, much patience and perseverance. But at <strong>the</strong> end, it pays <strong>of</strong>f with a<br />

<strong>model</strong> whose parameters are fully functionally interpretable, even on real<br />

data.<br />

Fitting and individual variations in growth<br />

A good fitting is not a criterion for deciding if a <strong>model</strong> is adequate<br />

(Fletcher, 1974). Choosing an inadequate <strong>model</strong> that fit <strong>the</strong> data very well<br />

is not problematic if that <strong>model</strong> is just used for descriptive purposes. It<br />

turns out to be a problem when parameters are functionally interpreted or<br />

if it is used in population dynamic simulations. In this case, individual<br />

variation should not be simply considered as an independent, normally<br />

distributed "error" whenever it is not. Individual variation has <strong>of</strong>ten been<br />

overlooked in <strong>the</strong> literature. The most aberrant calculations could result<br />

from such mistakes. For instance, Basuyaux & Blin (1998) extrapolated<br />

over 4 years a growth <strong>model</strong> for P. lividus where size distributions were<br />

supposed to be normal and using measurements from 7 to 23 months only.<br />

They calculated <strong>the</strong> fraction <strong>of</strong> <strong>the</strong> size distribution that would reach 40<br />

mm (<strong>the</strong> minimal market size) with time on basis <strong>of</strong> this extrapolation.<br />

Many techniques for population dynamic analyses are based on <strong>the</strong><br />

assertion that cohorts should distribute normally, including most recent<br />

ones (Smith & Botsford, 1998; Morgan et al, 2000) and could be also<br />

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

166

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