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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General conclusions<br />
component validates it as <strong>the</strong> basic process for <strong>the</strong> whole cohort and shows<br />
how intraspecific competition delays actual growth.<br />
<strong>Growth</strong> is <strong>the</strong> result <strong>of</strong> many complex mechanisms that interact:<br />
feeding, digestion, respiration, building up <strong>of</strong> new somatic tissues,<br />
maintenance, reproduction, etc. A general consensus is that growth is too<br />
complicated and could only be reliably described by complex <strong>model</strong>s.<br />
Indeed, it is surprising that a simple 2-parameter <strong>model</strong> like von<br />
Bertalanffy 1 (D(t) = D∞·[1 – e -k·t ]) could represent individual growth <strong>of</strong><br />
many organisms. It is also surprising that, considering interactions and<br />
individual variability in addition to <strong>the</strong> basic processes, a quite simple 5parameter<br />
<strong>model</strong> (our envelope curve, eq. 35 p 160) represents growth <strong>of</strong> a<br />
whole cohort <strong>of</strong> <strong>reared</strong> <strong>sea</strong> <strong>urchin</strong>s.<br />
Most <strong>of</strong> <strong>the</strong> simple <strong>model</strong>s <strong>of</strong> <strong>the</strong> first half <strong>of</strong> <strong>the</strong> twentieth century,<br />
attempt to interpret, in a functional way, ei<strong>the</strong>r individual growth (von<br />
Bertalanffy, 1938, 1957; Brody, 1945) or size/shape at age (Huxley, 1932;<br />
Teissier, 1934, 1948; d'Arcy Thompson, 1961). In <strong>the</strong> last half <strong>of</strong> <strong>the</strong><br />
century, <strong>the</strong>se <strong>model</strong>s have been replaced by more complex, but purely<br />
descriptive and/or speculative ones (Richards, 1959; Schnute, 1981;<br />
Tanaka, 1982, 1988; Jolicoeur, 1985). Clearly, it is worth revisiting old<br />
concepts using new tools, e.g., fuzzy logic or quantile regression. Such<br />
revisitation was accomplished for instance by van Osselaer & Grosjean<br />
(2000) in <strong>the</strong>ir study <strong>of</strong> <strong>the</strong> suture <strong>of</strong> coiled shells reflecting <strong>the</strong> ontogeny<br />
<strong>of</strong> molluscs. Despite <strong>the</strong> conclusion <strong>of</strong> Tursh (1998) that <strong>the</strong> shape <strong>of</strong> <strong>the</strong><br />
suture is too complex to be <strong>model</strong>led with a simple equation, <strong>the</strong>y<br />
demonstrated that a simple 4-parameter helicospiral <strong>model</strong> was <strong>the</strong> best<br />
descriptor for most coiled shells and that some methodological errors<br />
prevailed when using much more complex 8- to 16-parameter <strong>model</strong>s (for<br />
a review, see Stone, 1996). This example demonstrates ano<strong>the</strong>r case where<br />
growth is less complex in reality than in <strong>the</strong>ory. The discipline (call it<br />
"ontogenology") <strong>of</strong> describing individual growth or ontogeny with <strong>model</strong>s<br />
that are both reasonably simple and functional may reveal one day how<br />
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