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

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Capítulo 5<br />

At the <strong>en</strong>d of September of 2008, a sub‐sample of 15 seedlings from each<br />

factorial treatm<strong>en</strong>t was randomly s<strong>el</strong>ected from the three blocks. Whole seedlings<br />

were removed from the soil, and their roots washed and cleaned (second harvest). The<br />

mean root <strong>de</strong>pth was 28.4 ± 4.9cm. Total biomass was split into leaves, stems and<br />

roots, and morphological variables were calcu<strong>la</strong>ted by following the above‐<strong>de</strong>scribed<br />

procedure. Absolute shoot and root mean increm<strong>en</strong>ts were calcu<strong>la</strong>ted as the mean<br />

differ<strong>en</strong>ces betwe<strong>en</strong> shoot or root dry mass of each afforestation method at the<br />

second and first harvest. Shoot and root mean increm<strong>en</strong>ts for seedlings from directly<br />

sown seeds were tak<strong>en</strong> to be the shoot or root dry mass values obtained at the second<br />

harvest as no shoots or roots existed at seeding time. The r<strong>el</strong>ative growth rate (RGR)<br />

for each method was calcu<strong>la</strong>ted from the following expression (Hunt, 1990; Hoffman<br />

and Poorter, 2002):<br />

RGR = ln (M 2 ) – ln (M 1 )/(t 2 – t 1 )<br />

were ln (M 2 ) and ln (M 1 ) <strong>de</strong>note the mean ln‐transformed p<strong>la</strong>nt dry mass at time t 1 and<br />

t 2 , respectiv<strong>el</strong>y. M 2 and t 2 correspon<strong>de</strong>d to the second harvest for all afforestation<br />

methods, whereas M 1 and t 1 differed betwe<strong>en</strong> methods. For 1‐ and 3‐year‐old<br />

cultivated seedlings, M 1 and t 1 correspon<strong>de</strong>d to the first harvest before p<strong>la</strong>nting; for<br />

seedlings from directly sown seeds, M 1 and t 1 correspon<strong>de</strong>d to the first seeding<br />

harvest (after emerg<strong>en</strong>ce of seedlings). The standard <strong>de</strong>viation for RGR was calcu<strong>la</strong>ted<br />

according to Corn<strong>el</strong>iss<strong>en</strong> et al. (1996).<br />

Physiological mea<strong>sur</strong>em<strong>en</strong>ts<br />

Two types of mea<strong>sur</strong>em<strong>en</strong>ts were done: stomatal conductance and leaf water<br />

cont<strong>en</strong>t. A porometer (<strong>de</strong>lta T porometer AP4) was used to mea<strong>sur</strong>e leaf stomatal<br />

conductance. Mea<strong>sur</strong>em<strong>en</strong>ts were ma<strong>de</strong> every 2 weeks at midday (10–12 am so<strong>la</strong>r<br />

time) on four randomly s<strong>el</strong>ected replicates per species during the dry season (June to<br />

August 2008). Mea<strong>sur</strong>em<strong>en</strong>ts were ma<strong>de</strong> on complet<strong>el</strong>y expan<strong>de</strong>d young leaves<br />

receiving full sunlight.<br />

From May to October 2008, 10 seedlings per afforestation method were<br />

s<strong>el</strong>ected monthly for mea<strong>sur</strong>em<strong>en</strong>t of leaf water cont<strong>en</strong>t. A young leaf directly hit by<br />

sunlight was collected from each replicate. Leaves were rapidly transferred to<br />

141

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