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

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Capítulo 3<br />

Herb production in plot 2 was associated to light avai<strong>la</strong>bility and to<br />

establishm<strong>en</strong>t success for Q. pyr<strong>en</strong>aica in July (Fig. 4), i.e. this species was especially<br />

successful in zones with an abundant herbaceous cover.<br />

Figure 4. (A) Map of local covariance betwe<strong>en</strong> light avai<strong>la</strong>bility (GSF) and grass biomass in plot 2. (B)<br />

Map of local association betwe<strong>en</strong> grass biomass in plot 2 and establishm<strong>en</strong>t success of Q. pyr<strong>en</strong>aica in<br />

July. For a <strong>de</strong>scription of covariance patches and gaps, see Fig. 3B.<br />

Non spatial analysis of growth<br />

Interspecific and site differ<strong>en</strong>ces<br />

Stem height varied across species and plot, being in g<strong>en</strong>eral higher in plot 2 (P =<br />

0.01) (App<strong>en</strong>dix S2). Q. suber seedlings were the tallest. Abovegroung biomass and<br />

RGR a showed significant differ<strong>en</strong>ces across species. Q. faginea had the highest<br />

aboveground biomass and Q. pyr<strong>en</strong>aica the lower. RGR a was higher in Q. faginea and<br />

Q. suber. Leaf area, LMF a and RGR t were simi<strong>la</strong>r in differ<strong>en</strong>t species and plots<br />

(App<strong>en</strong>dix S2).<br />

Factors affecting growth and morphology<br />

Seed mass was one of the best predictors for growth and morphology as it<br />

appears in 39 % of the 48 mo<strong>de</strong>ls fitted (six variables per species and plot), being<br />

practically the only factor s<strong>el</strong>ected in mo<strong>de</strong>ls of plot 1 (Table 5) (see also App<strong>en</strong>dix 3).<br />

Figure 5 shows seed mass – aboveground biomass r<strong>el</strong>ations in plot 1.<br />

89

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