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In situ and Ex situ Conservation of Commercial Tropical Trees - ITTO

In situ and Ex situ Conservation of Commercial Tropical Trees - ITTO

In situ and Ex situ Conservation of Commercial Tropical Trees - ITTO

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319ratios that deviated from Hardy-Weinberg estimation due to a lack <strong>of</strong>heterozygotes.Fixation indexHigh homozygosity was observed from positive fixation indices in seedlingsamples that may have been produced through selfing or half-sib mating. Thishad also been shown through a study on Pinus sp. (Muona 1989). Accordingto Muona (1989), positive fixation indices at the seedling level might be due toself-pollination. Seedlings produced through inbreeding usually die <strong>of</strong>f beforematurity as they are weaker. This follows the theory <strong>of</strong> natural selection, whichstates that selection is the dominant force in evolution (Hartl 1980). <strong>Ex</strong>cess <strong>of</strong>heterozygosity in locus Shc02 as shown by a negative value might mean thatthis locus responds to selection pressure <strong>and</strong> may be linked to adaptive traits.The Wahlund Effect (1928) states that natural populations that aredivided into sub-populations might have allele frequencies that deviate frompopulations due to natural selection, or r<strong>and</strong>om genetic drift in the case <strong>of</strong> smallpopulations. The effect is that the homozygous genotype frequency <strong>of</strong> the wholepopulation exceeds Hardy-Weinberg equilibrium, whereas heterozygotes <strong>of</strong> thewhole population decrease from the Hardy-Weinberg ratio. <strong>In</strong> the case <strong>of</strong> D.aromatica, it could be said that all the populations in Peninsular Malaysiaoriginated from one large population that had been sub-divided into a few subpopulations.This would explain the high fixation indices observed in all D.aromatica populations.Genetic diversity in D. aromatica populationsOn the whole, the five populations showed a high level <strong>of</strong> genetic diversity. Out<strong>of</strong> the seven microsatellite loci studied, 40 alleles were observed, which is amean <strong>of</strong> 5.14 ± 0.20 alleles per locus. This value is higher than those obtainedfrom isozyme markers for conifers (2.29) <strong>and</strong> tropical species (2.02) (Hamrick<strong>and</strong> Loveless 1989). D. aromatica, using isozyme markers, gave a value <strong>of</strong> 4.1(Lee et al. 2000b). Generally, microsatellite markers yield a high number <strong>of</strong>alleles per locus due to length mutations that causes differences in repeat units.Amos et al. (1993) obtained 54 alleles from one whale microsatellite locus <strong>and</strong>Fornage et al. (1992) obtained 15 alleles in one locus located on the first intron<strong>of</strong> the C-II apoliprotein gene in a French human population.<strong>Ex</strong>pected heterozygosity was more than the observed value by 0.218,showing an excess <strong>of</strong> homozygotes. This may be because leaf samples <strong>of</strong>seedlings were used in this study. <strong>Ex</strong>pected heterozygosity (H e= 0.709) was

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