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

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Capítulo 2<br />

<strong>de</strong>eper <strong>la</strong>yers of the soil, in which there are more water resources avai<strong>la</strong>ble (Milberg<br />

and Lamont, 1997). In addition, they have a greater aboveground growth, which<br />

permits them to <strong>de</strong>v<strong>el</strong>op a <strong>la</strong>rger photosynthetic <strong>sur</strong>face.<br />

Quero et al. (2007) have suggested that the three hypotheses are connected.<br />

Therefore, the r<strong>el</strong>ationship betwe<strong>en</strong> the seed and the seedling biomass is mediated by<br />

two effects: the use of the reserves and the metabolic effect. Increasing the use of<br />

reserves has a positive effect on seedling biomass, but a strong metabolic effect (a<br />

negative r<strong>el</strong>ationship betwe<strong>en</strong> RGR and seed mass) could lead to a <strong>la</strong>ck of any<br />

r<strong>el</strong>ationship betwe<strong>en</strong> seed mass and seedling biomass. Most studies on the<br />

implications of the variation in seed size have be<strong>en</strong> carried out by comparing differ<strong>en</strong>t<br />

species. Differ<strong>en</strong>ces in mean seed‐size betwe<strong>en</strong> species have be<strong>en</strong> interpreted as<br />

being differ<strong>en</strong>tial adaptations to a wi<strong>de</strong> spectrum of ecological niches (Westoby et al.,<br />

1996). However, studies at an intra‐specific lev<strong>el</strong> are also of interest, since they can<br />

provi<strong>de</strong> a better un<strong>de</strong>rstanding of the effect of variation in seed size on seedling<br />

establishm<strong>en</strong>t (Bonfil, 1998). Many studies have <strong>de</strong>tected intra‐specific variations in<br />

mean seed size within and betwe<strong>en</strong> popu<strong>la</strong>tions (Micha<strong>el</strong>s et al., 1988; Ågr<strong>en</strong> and<br />

Gr<strong>en</strong>, 1989; Susko and Lovett‐Doust, 2000; Castro et al., 2008; Rámirez‐Vali<strong>en</strong>te et al.,<br />

2009). This variability is also reflected in other characters like germination or aerial<br />

biomass (Sills and Ni<strong>en</strong>huis, 1995; Castro et al., 2008). This betwe<strong>en</strong>–p<strong>la</strong>nt variability<br />

seems to be due to g<strong>en</strong>etic differ<strong>en</strong>ces betwe<strong>en</strong> mother p<strong>la</strong>nts as w<strong>el</strong>l as <strong>en</strong>vironm<strong>en</strong>t<br />

conditions pres<strong>en</strong>t at the mom<strong>en</strong>t of the seed’s <strong>de</strong>v<strong>el</strong>opm<strong>en</strong>t (Wulff, 1986; Ågr<strong>en</strong> and<br />

Gr<strong>en</strong>, 1989; Baskin and Baskin, 2001; Castro et al., 2008; Souza et al., 2010).<br />

<strong>Quercus</strong> g<strong>en</strong>us has high g<strong>en</strong>etic diversity (Michaud et al., 1992), and ph<strong>en</strong>otypic<br />

p<strong>la</strong>sticity (Quero et al., 2008b). The exist<strong>en</strong>ce of inter‐individual variation in acorn<br />

yi<strong>el</strong>ds has be<strong>en</strong> studied for differ<strong>en</strong>t species (Ramírez and Gómez, 1982; Ducousso et<br />

al,. 1993; Gómez 2004a). In fact, acorn size is a factor traditionally used for the<br />

s<strong>el</strong>ection of trees in op<strong>en</strong> forest areas (<strong>de</strong>hesas) (Vazquez, 1998). Tilki and Alptekin<br />

(2005) found differ<strong>en</strong>ces in germination rates among <strong>Quercus</strong> aucheri seeds from<br />

differ<strong>en</strong>t prov<strong>en</strong>ances. Fernán<strong>de</strong>z‐Rebollo et al. (2008) have found differ<strong>en</strong>ces in acorn<br />

moisture perc<strong>en</strong>tage and chemical composition within popu<strong>la</strong>tions of Q. ilex. This high<br />

53

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