A protocol is described for plantlet regeneration using embryonic expl
ants of Juniperus cedrus Webb and Berth. An average of 6 adventitious
buds were induced on whole excised embryos cultured for 15 days on Quo
irin and LePoivre (QP) half-strength medium supplemented with 5 mu M N
-6-benzyladenine. For bud development, explants were transferred to ph
ytohormone-free 1/2 QP medium. For shoot elongation, explants were cul
tured on 1/2 QP with 0.05% activated charcoal and 2% sucrose. Adventit
ious shoots were rooted successfully in pear-vermiculite-perlite(1:1:1
) moistened with 1/4 QP containing 1% sucrose and 5 mu M alpha-napthal
eneacetic acid, pH 5.0. Axillary shoots elongated spontaneously in cul
ture from leaf axils.