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
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
General conclusions<br />
individuals, whose inhibition is suddenly eliminated, could quickly replace<br />
missing adults. Two conditions should be met, however, to obtain this<br />
result on <strong>the</strong> long term. First, mortality <strong>of</strong> small and mid-sized individuals<br />
should not increase when large adults are removed (indeed, when<br />
removing large adults, <strong>the</strong> passive protection <strong>of</strong> small individuals against<br />
predators disappears). If necessary, part <strong>of</strong> <strong>the</strong> adults should be left in<br />
place during harvesting. Second, recruitment should not be a limiting<br />
factor. By harvesting large adults before <strong>the</strong>y spawn, recruitment is de<br />
facto lowered. An artificial production <strong>of</strong> a large amount <strong>of</strong> seed in<br />
hatcheries is one way to maintain recruitment levels. Beyond <strong>the</strong>se general<br />
considerations, it is difficult to define rules for sustainable fishery<br />
practices. If <strong>the</strong> growth <strong>model</strong> with intraspecific competition were<br />
calibrated against field population data, it would be possible to quantify<br />
<strong>the</strong> impact <strong>of</strong> various fishery methods, and to provide objective criteria for<br />
sustainable <strong>sea</strong> <strong>urchin</strong> fisheries (Grosjean & Jangoux, 2000).<br />
From a <strong>the</strong>oretical point <strong>of</strong> view, <strong>the</strong> new growth <strong>model</strong> rehabilitates a<br />
60-year old <strong>the</strong>ory <strong>of</strong> growth elaborated by von Bertalanffy (1938). Since<br />
<strong>the</strong>n, several authors have questioned its validity (Knight, 1968; R<strong>of</strong>f,<br />
1980; Frontier & Pichot-Viale, 1993). Many o<strong>the</strong>r works have indicated<br />
that <strong>the</strong> von Bertalanffy 1 <strong>model</strong> is probably not acceptable to describe <strong>the</strong><br />
growth <strong>of</strong> <strong>sea</strong> <strong>urchin</strong>s (Gage & Tyler, 1985; Gage et al, 1986; Gage, 1987;<br />
Dafni, 1992; Ebert, 1980a; Ebert & Russell, 1993; Lamare & Mladenov,<br />
2000), including P. lividus (Cellario & Fenaux, 1990; Turon et al, 1995).<br />
Here we have shown that sigmoidal growth does not necessarily means<br />
that von Bertalanffy's <strong>the</strong>ory is invalid. An S-shape could result from<br />
inhibition <strong>of</strong> growth at small sizes/ages. P. lividus follows <strong>the</strong> von<br />
Bertalanffy's law for its somatic growth when it is not inhibited. In a<br />
cohort, <strong>the</strong> non-inhibited fraction amounts for less than 10% <strong>of</strong> all <strong>the</strong><br />
individuals. Using least-square regression leads to <strong>the</strong> rejection <strong>of</strong> <strong>the</strong> von<br />
Bertalanffy 1 <strong>model</strong>. Using quantile regression validates it for <strong>the</strong> largest<br />
fraction. Using an envelope <strong>model</strong> with intraspecific competition<br />
182