Genetic diversity at 11 loci encoding nine enzymes was studied in 23 populations of Japanese beech Fagus crenata Blume distributed throughout the range of the species. Levels of genetic diversity were high for both within species (expected mean heterozygosity: 0.194) and within populations (expected mean heterozygosity: 0.187), whereas the level of genetic diversity among populations was low ( GsT = 0.038), as observed in various long-lived, woody plants.Despite the low differentiation among populations, geographical patterning of the variation was observed. Populations in south-western Japan tended to have greater within-population variation and to be more highly differentiated when compared with those in north-eastern Japan. In addition, allele frequencies observed at eight loci were significantly related to latitudinal and/or longitudinal gradients and showed clinal variation across the range of the species. Principal components analysis revealed that the populations tended to cluster according to their geographical locations. The nonrandom patterns of variation were probably shaped by relatively recent historical events such as late-Quaternary migration and founding events.

Nine simple sequence repeat (SSR) markers were developed from Shorea curtisii using two different methods. One SSR locus was isolated by the commonly used method of screening by colony hybridization, and the other eight loci were isolated by a vectorette PCR method. Primer pairs were designed based on the sequences of all these SSR loci. Analysis of 40 individuals of S. curtisii from natural forest in Malaysia revealed that all SSR loci were polymorphic. Four SSR markers, Shc01, Shc04, Shc07 and Shc09, were highly polymorphic. We have also tested the applicability of these SSR printers to other species of Dipterocarpaceae using PCR amplification. Because the flanking region sequences of the S. curtisii SSRs were well conserved within this family, the SSR primers for S. curtisii can be applied to almost all species of Dipterocarpaceae.