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Establecimiento de cuatro especies de Quercus en el sur de la ...

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Capítulo 2<br />

more advanced ontog<strong>en</strong>etic phase, in which seed‐mass effects might be masked with<br />

photosynthetic gains. Light conditions may influ<strong>en</strong>ce the seedling‐size effect, as this<br />

effect was mainly observed un<strong>de</strong>r mo<strong>de</strong>rate or <strong>de</strong>nse sha<strong>de</strong> conditions by Quero et al.<br />

(2007) and Leishman and Westoby (1994). However, Chacón and Bustamante (2001)<br />

and Quero et al. (2008a), found the seedling size effect un<strong>de</strong>r differ<strong>en</strong>t <strong>en</strong>vironm<strong>en</strong>t<br />

conditions: both in drought and irrigation regimes, the <strong>la</strong>tter being comparable to the<br />

conditions in our study.<br />

Consi<strong>de</strong>ring the mother tree, at least for one mother tree per species, the<br />

seedling‐size effect was not found. It seems that, regardless of the seed size, there are<br />

other factors r<strong>el</strong>ated to maternal influ<strong>en</strong>ce. Differ<strong>en</strong>t causes could be responsible for<br />

this, such as a differ<strong>en</strong>t chemical composition of the seeds, effici<strong>en</strong>cy of reserve use or<br />

biomass allocation (Leiva and Fernán<strong>de</strong>z‐Alés, 1998; Rodríguez‐Estévez et al., 2008).<br />

To summarize, an int<strong>en</strong>sive use of the reserves <strong>de</strong>termined <strong>la</strong>rger seedlings in<br />

the first <strong>de</strong>v<strong>el</strong>opm<strong>en</strong>t stages, as in the case of M 4 of Q. faginea, or M 5 of Q. ilex (Fig. 3).<br />

These results <strong>en</strong>courage the i<strong>de</strong>a that the production of <strong>la</strong>rger seedlings from <strong>la</strong>rger<br />

seeds is more r<strong>el</strong>ated to the amount of reserves stored in the cotyledons and their use<br />

rather than to the initial growth rates (Baskin and Baskin, 2001; Castro et al., 2008).<br />

However, for some mother trees, the metabolic effect showed up (M 4 and M 5 of Q.<br />

pyr<strong>en</strong>aica or M 1 of Q. suber) and this was the cause of the <strong>la</strong>ck of r<strong>el</strong>ationship betwe<strong>en</strong><br />

seed mass and seedling biomass. This was predicted by the mo<strong>de</strong>l of Quero et al.<br />

(2007). For other mother trees (M 2 of Q. faginea) neither the metabolic effect nor the<br />

seedling effect were found. For some reason, these p<strong>la</strong>nts were less effici<strong>en</strong>t in the use<br />

of their reserves. The chemical composition and proportion of carbohydrates in the<br />

seeds or the respiration rates during germination could offer some exp<strong>la</strong>nation.<br />

Assessing maternal influ<strong>en</strong>ces<br />

As <strong>de</strong>scribed above, we found differ<strong>en</strong>t tr<strong>en</strong>ds betwe<strong>en</strong> mother trees wh<strong>en</strong><br />

evaluating seed mass effects, and maternal origin seems to <strong>de</strong>termine other traits<br />

acting in<strong>de</strong>p<strong>en</strong><strong>de</strong>ntly from the seed size, such as acorn g<strong>en</strong>etic variability or<br />

physiological status (Merouani et al., 2001; Goodman et al., 2005). This i<strong>de</strong>a is<br />

corroborated by other studies in which a mother effect in Q. ilex on characteristics<br />

67

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