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

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Spatial and temporal heterog<strong>en</strong>eity effects on seedling growth and establishm<strong>en</strong>t in four <strong>Quercus</strong> species<br />

mass to leaf area. Because LMA <strong>de</strong>p<strong>en</strong>ds on both the particu<strong>la</strong>r species and inci<strong>de</strong>nt<br />

light (Aranda et al., 2004; Poorter et al., 2009), linear regressions betwe<strong>en</strong> LMA and<br />

light avai<strong>la</strong>bility (Global Site Factor, GSF) were calcu<strong>la</strong>ted for each species in or<strong>de</strong>r to<br />

obtain accurate estimates of LMA in r<strong>el</strong>ation to GSF (r 2 > 0.40). LMA and the leaf area<br />

estimates were used to calcu<strong>la</strong>te leaf dry mass per seedling.<br />

At the <strong>en</strong>d of the growth season (July 2007), <strong>de</strong>ad seedlings were harvested for<br />

calcu<strong>la</strong>tion of stem and leaf dry weight. No significant differ<strong>en</strong>ces in spring aerial<br />

seedling biomass were found betwe<strong>en</strong> <strong>sur</strong>viving seedlings after summer and <strong>de</strong>ad<br />

seedlings. Therefore, seedling biomass of <strong>de</strong>ad seedlings could be assumed as<br />

repres<strong>en</strong>tative of the popu<strong>la</strong>tion. In those seedlings mea<strong>sur</strong>ed on both sampling dates<br />

(beginning and <strong>en</strong>d of the growth season) stems r<strong>el</strong>ative growth rate (RGR t ) and<br />

aboveground r<strong>el</strong>ative growth rate (RGR a ) was calcu<strong>la</strong>ted as:<br />

(1) RGR = (lnM 2 – lnM 1 ) / t ,<br />

were M 1 and M 2 were biomass (aboveground or stems) at the beginning and at the<br />

<strong>en</strong>d of the growing season, respectiv<strong>el</strong>y, and t is the time interval betwe<strong>en</strong> the two<br />

mea<strong>sur</strong>em<strong>en</strong>ts. Aerial leaf mass fraction (LMF a ) was calcu<strong>la</strong>ted at the <strong>en</strong>d of the<br />

growth season (t 2 ) as:<br />

(2) LMF a = M l / M t ,<br />

were M l was leaf mass and M t was total aboveground biomass, both estimated at t 2 .<br />

Environm<strong>en</strong>tal variables (light avai<strong>la</strong>bility, soil moisture and herb production)<br />

were mea<strong>sur</strong>ed at each no<strong>de</strong>. For simplicity, herb prodution was named as<br />

“<strong>en</strong>vironm<strong>en</strong>tal variable” because it was studied as an external factor that may<br />

influ<strong>en</strong>ce seedling growth and establishm<strong>en</strong>t. Light avai<strong>la</strong>bility was estimated via the<br />

Global Site Factor (GSF) (Rich, 198), using hemispherical photographs tak<strong>en</strong> with a<br />

Coolpix camera fitted with an FC E8 fisheye l<strong>en</strong>s, both from Nikon (Tokyo, Japan), in<br />

the spring of 2007. Photograhps were processed with the software Hemiview Canopy<br />

Analysis v. 2.1 (D<strong>el</strong>ta‐T, Cambridge, UK). Soil moisture was mea<strong>sur</strong>ed as the volumetric<br />

cont<strong>en</strong>t of water at each sampling point on a monthly basis from February to<br />

September 2007. Mea<strong>sur</strong>em<strong>en</strong>ts were ma<strong>de</strong> with a TDR (Mo<strong>de</strong>l 100, Spectrum<br />

Technologies, Inc., P<strong>la</strong>infi<strong>el</strong>d, IL, USA) fitted with 20 cm long rods ─by exception, the<br />

80

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