To develop an efficient procedure for plant regeneration from leaf-derived callus of Lavandula
vera DC, the production of multiple shoots and the formation of roots from these shoots were
studied. When calli were cultured in a medium with 4.010 7 M N-(2-chloro-4-pyridyl)-N0-
phenylurea (CPPU), urea-type cytokinin, multiple shoots were obtained from the greenish surface
of the callus ef®ciently at a rate of 52.2%. For multiple shoot development, the shoots were divided into 7±20 shoot clusters with 2±3 shoots and subcultured every 2 weeks. Two modi®ed culturesystems were employed for subculture; a ``closed culture system'' and an ``open culture system''. In the open-system, shoot clusters grew and elongated vigorously. In the closed-system, most of the clusters showed vitri®cation and did not elongate. In root induction culture, shoot clusters in the open-system were well rooted and grew vigorously, the highest rate of root formation being 74.0%,in the 1 2 MS medium supplemented with 1.010 ÿ6 M indoleacetic acid (IAA). On the other hand,shoot clusters in the closed-system showed vitri®cation and did not root well. About seven times more regenerants were obtained from the multiple shoots than from normal shoots treated with 4.410 ÿ6 M 6-benzylamino purine (BA), a purine-type cytokinin. These results indicate that ef®cient plant regeneration in L. vera from callus using multiple shoots is possible by means of an open-system.