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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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363manan indicated that there were five loci correlated with the growth <strong>of</strong> seedlings<strong>of</strong> that species (Salwana et al. 1996). By identifying the linkage betweenquantitative characters <strong>and</strong> isozyme markers, tree improvement programs couldbe initiated at very early ages, thus contributing to more efficient use <strong>of</strong> bothhuman resources <strong>and</strong> finances. <strong>In</strong> addition to provenance considerations,information on genetic linkage would assist conservation programs <strong>and</strong>sustainable utilization <strong>of</strong> P. falcataria by guiding development <strong>of</strong> appropriateplantation programs in <strong>In</strong>donesia.Impact <strong>of</strong> logging on genetic diversity <strong>of</strong> S. laevis, parvifolia <strong>and</strong> E.zwageriiResults based on isozyme, RAPD, <strong>and</strong> AFLP analyses <strong>of</strong> S. parvifolia <strong>and</strong> E.zwagerii indicated that logging has not had significant effects on reducing geneticdiversity <strong>of</strong> either species. However, results suggested that it may effect futuregenetic diversity, which means that precautions must to be taken. This studyalso indicated that the three techniques used led to the same conclusion, althoughthey gave slightly different results in terms <strong>of</strong> clustering or grouping. Thedifferences found between the techniques for genetic relatedness betweenindividuals <strong>and</strong> for variation patterns <strong>of</strong> individuals within the group, werepresumably due to differences in evolution rates which affect the geneticvariation pattern (Baruffi et al. 1995). According to Williams et al. (1990) theDNA sampling region for the RAPD assay is less responsive to selection,which leads to a higher degree <strong>of</strong> resistance to mutation than DNA coding forisozymes. The different results obtained from RAPD <strong>and</strong> from AFLP wereprobably due to the result <strong>of</strong> r<strong>and</strong>om sampling <strong>of</strong> total genome <strong>and</strong> the result <strong>of</strong>functional protein (Peakall et al., 1995). It is suggested that the use <strong>of</strong> thesetechniques can be applied complementary to each other. <strong>In</strong>itial analysis can becarried out using isozyme or RAPD, then AFLP may be used for further analysisto determine those groupings still not clear. Combinations <strong>of</strong> various markerswill give a better estimate <strong>of</strong> genetic correlation between individuals <strong>and</strong> couldproduce a genetic structure hierarchy based on empirical data.Results also suggest that, based on RAPD <strong>and</strong> AFLP analysis <strong>of</strong> S.parvifolia <strong>and</strong> E. zwagerii, there were no significant differences betweenlogged <strong>and</strong> unlogged areas in all parameters <strong>of</strong> genetic diversity observedalthough all values for E. zwagerii were reduced in the logged area (Table 3).Logging practices are therefore an important factor in terms <strong>of</strong> decreasinggenetic diversity in natural populations. Threshold values need to be determinedfor each species <strong>and</strong> used for implementation <strong>of</strong> appropriate conservationprograms for <strong>In</strong>donesian species.

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