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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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A Study <strong>of</strong> Genetic Variation Using AFLP Techniquein Populations <strong>of</strong> K<strong>and</strong>elia c<strong>and</strong>el in Ryukyu Isl<strong>and</strong>s<strong>and</strong> Southern Japan325KO HARADA AND TAKANORI AZECHIDepartment <strong>of</strong> Forest Resources, Faculty <strong>of</strong> Agriculture, Ehime University3-5-7 Tarumi, Matsuyama, 790-8566 Japankharada@agr.ehime-u.ac.jpAbstract. To examine the extent <strong>of</strong> genetic variation within <strong>and</strong> among populations <strong>of</strong> K<strong>and</strong>eliac<strong>and</strong>el, AFLP analysis was applied to 7 populations from the Ryukyu Isl<strong>and</strong>s <strong>and</strong> SouthernJapan. A total <strong>of</strong> 553 b<strong>and</strong>s were detected using 4 selective primer pairs. The proportion <strong>of</strong>polymorphic loci <strong>and</strong> the average heterozygosity for each population ranged from 29.8 to58.2%, <strong>and</strong> from 0.067 to 0.152, respectively. Mean average heterozygosity (H) <strong>and</strong> nucleotidediversity (π) are 0.099 <strong>and</strong> 0.0098, respectively. The nucleotide diversity shown here is in therange <strong>of</strong> 52 to 80% <strong>of</strong> the values shown in that <strong>of</strong> the moderate temperate forests <strong>of</strong> Japanesebeech (Fagus crenata) <strong>and</strong> Japanese oak (Quercus mongolica var. grosseserrata); however, thefixation index (G ST) was shown to be 0.151, larger than the value shown in oak (0.083), <strong>and</strong>indicating considerable genetic differentiation among populations. The Iriomote-jima populationshowed the largest variation in both H <strong>and</strong> π. The UPGMA tree was constructed based onnucleotide diversities <strong>and</strong> showed no association with geographic distance. This result suggeststhat gene flow rate by seed migration is not simply correlated with the geographic distancebetween isl<strong>and</strong>s. The Kiire population is possibly a man-made population.<strong>In</strong>troductionSpecies are composed <strong>of</strong> genetically diverse individuals; that is to say, geneticvariation has been accumulated in populations. It has been said that geneticvariation is the source <strong>of</strong> adaptive evolution in a changing environment <strong>and</strong> it isthus important for a population to maintain its adaptive <strong>and</strong> evolutionary potential(Newton et al. 1999). The extent <strong>of</strong> genetic variation depends on the length <strong>of</strong>time the population has been established, the population size, <strong>and</strong> the mutationrate. Subdivided populations have been processed by both r<strong>and</strong>om genetic drift<strong>and</strong> natural selection to adapt to different environments. They have thenaccumulated genetic variation in different combinations <strong>of</strong> alleles <strong>and</strong> havebecome genetically diversified. These processes have been studied by usingelectrophoresis to detect protein polymorphism since the experiments <strong>of</strong> Lewontin<strong>and</strong> Hubby (1968) in Drosophila <strong>and</strong> Harris in humans (1966). Recently,however, a method called PCR has been more commonly used for these studiesto detect genetic variation at the DNA level. Variations at the DNA level, such

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