Rooting of shoots derived from axillary buds was examined to establish an efficient shoot culture system of clonal micropropagation in adult tree of Larix leptolepis Gord. (Japanese larch). Nine out of ten shoots induced calli (90%) on their shoot bases, and the two of them formed root primordia with a red pigment (20%) on the calli surface within 5 weeks after culturing on modified Murashige and Skoog (MS) medium supplemented with 1.5 btM of indolebutyric acid (1BA) and 1.5 laM of naphthaleneacetic acid (NAA). However, the primordia did not elongate actively. The addition of 10 mM L-phenylalanine in the MS medium with the auxins resulted in the formation of roots at high fi'equency, about 80%, and they elongated actively. Although callus was formed in all the shoots cultured on the medium with L-phenylalanine, it appeared that the callus development was less as compared to the medi um without L-phenylalanine. Consequently, the rooting might be associated with the suppression of the induced callus.Key words : adult tree, LarLv leptolepis, L-phenylalanine, root formation Establishment of a clonal propagation system by tissue culture is very important to produce the dominant trees, in points of yield, quality, adaptability and resistance. A cutting, which is one of asexual propagation method, has been generally practiced for genetic improvement of species such as C13~ptomeria japonica and Chamaecyparis obtusa (Mikami, 1991). These species can root in vitro (Ishikawa, 1986;Amano, 1989). However, in some other species such as Larix leptolepis, it is difficult to induce roots directly in the cuttings, or in vitro, in case of using shoots from the adult tree. It is reported that the rate of rooting was less than 30% in shoots of trees over 10-year-old (Ishikawa, 1962;Okada, 1967). Thus, the authors attempted to establish a new propagation system by shoot culture for theimprovement of rooting in the adult tree of L. leptolepis.In L leptolepis, bud culture has been achieved in vitro (Itahana, 1993), but the explant is confined to an apical bud in shoots. Tissue culture of axillary buds in shoots from an adult tree is an effective method to propagate the dominant trees.However, it seems that achievement is not notable in L. leptolepis, compared with such species as C. obtusa, Piing brutia, Pinus radiata (Amano, 1989;Abdullah et al., 1987;Horgan and Holland, 1989). This may be lmgely due to heavy contamination which occurs peculiarly in the adult tree of Larix species. The problem has been partly solved by authors who investigated for conditions to effectively sterilize the explants and also for culture conditions to flush more frequently axillary buds in shoots from an adult tree of L. leptolepis of more than 20-year-old (Ogita et al., 1995). Another problem is the fact that the rooting percentage is remarkably poor in shoots originating from axillary buds of adult tree. It has been generally known that root formation in shoot culture of woody plants is mainly controlled by some kind of auxin and its concentration in a su...