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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It does not consider respiration associated with gonadal growth or<br />
gametogenesis. There are two possibilities for mature individuals: ei<strong>the</strong>r<br />
gonadal growth competes with somatic growth (and <strong>the</strong> later should be<br />
lower than predicted while β remains 0.67) or it just adds to it (and β<br />
should be somewhat larger). Giese et al (1966) measured no difference in<br />
<strong>the</strong> respiration <strong>of</strong> S. purpuratus in function <strong>of</strong> gonad index. This could<br />
indicate a competition between somatic and gonadal growth in <strong>the</strong><br />
presence <strong>of</strong> a limiting factor. However, it should imply a different somatic<br />
growth <strong>model</strong> for juveniles and adults. In <strong>the</strong> present case, a single <strong>model</strong><br />
fits both juvenile and adult stages for <strong>reared</strong> P. lividus. Measurements <strong>of</strong><br />
respiration and a more accurate comparison between both phases are<br />
required to evidence a possible effect <strong>of</strong> maturity on <strong>the</strong> somatic growth<br />
curve. In any case, β-values between 0.6 and 0.8 do not contradict von<br />
Bertalanffy's law. Thus, <strong>the</strong> present study rehabilitates its <strong>the</strong>ory that was<br />
too <strong>of</strong>ten rejected after observation <strong>of</strong> a sigmoidal growth (and now we<br />
know it could result from an inhibition).<br />
Functional analysis <strong>of</strong> <strong>the</strong> constrained parameters<br />
Constraining <strong>the</strong> <strong>model</strong> to <strong>the</strong> origin is very easy, in <strong>the</strong>ory. Most<br />
<strong>model</strong>s in Table 12 and also eq. 29 have a free intercept. It could be<br />
formally expressed: D0 in eq. 29, or it could be hidden in <strong>the</strong><br />
parameterization: a⋅(1 – e bc ) for von Bertalanffy 1, a - d for Weibull, for<br />
<strong>model</strong>s <strong>of</strong> Table 12. Unconstrained intercept means <strong>the</strong> parameter<br />
representing size when <strong>the</strong> growth process initiates is estimated at <strong>the</strong> same<br />
time as all o<strong>the</strong>rs, and is thus influenced by <strong>the</strong>ir values (intercorrelation).<br />
In real life, <strong>the</strong> initial size can influence following growth (for some<br />
experimental studies on P. lividus, see Vaïtilingon et al, 2001). We believe<br />
that a meaningful <strong>model</strong> should follow <strong>the</strong> same logic: initial size is fixed<br />
first and parameters that characterize growth are estimated afterwards.<br />
This is done in eqs. 30-31. Of course, "initial" size just after<br />
metamorphosis is <strong>the</strong> result <strong>of</strong> ano<strong>the</strong>r growth process during larval life but<br />
<strong>the</strong> <strong>model</strong> describes postmetamorphic growth, not larval growth.<br />
Part IV: A growth <strong>model</strong> with intraspecific competition<br />
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