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In general, all genetic variability studies revealed a low estimate among stands diversity as well as a low<br />
geographic structure (Leonardi, Menozzi 1996) with a consequential strong diversity component<br />
within population. These findings are consistent with the European stand data and wind-pollinated,<br />
low self-compatibility reproductive biology, characterized by a low level (2 – 4%) of inbreeding<br />
(Rossi, Vendramin, Giannini 1996).<br />
Emiliani et al. (2004) using RAPD and cpDNA PCR-RFLP markers analyzed 30 populations located<br />
in southern Italy. The analysis showed that the south of Italy represents a diversity hotspot with<br />
more than one glacial (micro) refuge nuclei, and that the genetic variability among populations is<br />
substantially higher than that reported in literature.<br />
In a wi<strong>de</strong>r geographic context, the distribution of chloroplast DNA (cpDNA) variation was studied<br />
using PCR-RFLP and microsatellite markers in 6 Italian beech populations (Vettori et al. 2004).<br />
The authors confirm the role of southern and central Italy as the hotspots of haplotype diversity<br />
(highest level of total haplotype diversity h = 0.822, high level of genetic differentiation g = 0.855)<br />
t st<br />
and the highest number of haplotypes. Nevertheless, all haplotypes found along the Apennines<br />
remained trapped in the Italian peninsula.<br />
The phylogeography of beech was extensively analyzed with molecular genetics and paleobotanical<br />
approaches by Magri et al. (2006) suggesting, in accordance with Emiliani et al. (2004) and Vettori<br />
et al. (2004), that beech populations might have survived during the last glacial period at different<br />
locations in the Italian peninsula, with the consequence that no clear large-scale migration trends<br />
can be recognized in southern and central Italy. Furthermore the authors suggest that the presence<br />
of populations displaying high divergence in central-southern Italy may be associated to the fact that<br />
beech populations persisted in these regions since the middle Pleistocene.<br />
Recently, microsatellite loci were used to examine the impact of forest management on genetic<br />
diversity (Buiteveld et al. 200 ). The comparison between two Italian stands – one near to the<br />
‘old-growth’ forest and one with high management-intensity (shelterwood system) – revealed no<br />
significant differences in genetic diversity parameters.<br />
Using an innovative approach on fossil pollen DNA, Paffetti et al. (200 ) <strong>de</strong>monstrated, in contrast<br />
to current knowledge based on palynological and macrofossil data, that the F. orientalis complex<br />
was already present during the Tyrrhenian period in what is now Venice lagoon (Italy). This finding<br />
represents a new and important insight, consi<strong>de</strong>ring that nowadays Western Europe is not the natural<br />
area of the Fagus orientalis complex, and that the presence of the complex during the last interglacial<br />
period in Italy has never been hypothesized before.<br />
The individuation of retrotransposable elements in beech (Emiliani, Paffetti, Giannini 2009)<br />
offers an interesting insight into F. sylvatica genome and the possibility for the <strong>de</strong>velopment of new<br />
markers for genetic diversity screening and for evolution studies.<br />
A genetic linkage map of European beech was constructed according to a “two-way pseudo-testcross”<br />
mapping strategy, using a total of 312 RAPD, AFLP and SSR markers scored in 143 individuals from<br />
a F full-sib family (Scalfi et al. 2004). In the same pedigree, the association with genetic markers of<br />
1<br />
several quantitative traits: leaf area, leaf number and shape in two different years, specific leaf area,<br />
leaf carbon-isotope discrimination and tree height were also investigated obtaining QTLs associated<br />
with leaf traits explaining a variation between 15% and 35%.<br />
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