Crinum lilies (Crinum spp. L.) are tropical and sub-tropical bulbous plants
with excellent potential for southern US landscapes. Unfortunately, the mo
re desirable crinum cultivars are slow and expensive to propagate by tradit
ional offsets. The objective of this research was to develop reliable proce
dures for multiplying Crinum 'Ellen Bosanquet' by tissue culture. A sterili
zation procedure for cleaning explants was developed in which bulb chips co
ntaining a basal plate were submersed and agitated in 0.525% hypochlorite f
or 1 h. For shoot formation, tri-scales (three scales attached to a section
of the basal plate) were used as the explant source and grown on MS-based
media containing five levels of benzyladenine (BA) (0-22.2 mu M) and five l
evels of naphthaleneacetic acid (NAA) (0-5.3 mu M) The greatest shoot forma
tion was obtained from the highest level of BA (22.2 mu M) without NAA. In
a subsequent experiment, explants were cultured for 4 months on media conta
ining 35.5-88.8 mu M BA, and then transferred to hormone-fret media for 3 m
onths. BA at 35.5 mu M stimulated optimal shoot (8.4) and bulblet (2.8) for
mation. Plantlets were successfully acclimatized and rooted ex vitro. (C) 1
999 Elsevier Science B.V. All rights reserved.