ABSTRACT
In vitro flowering was successfully induced from the shoots regenerated in cultures of Aerva
lanata. In vitro flowering method can be monitored effectively in studying floral transition and flower
development from vegetative to reproductive phase. The nodal shoot segments were used as explants
in the present study. The explants were surface sterilized using HgCl2 and inoculated on Murashige
and Skoog’s (MS) medium supplemented with 6-benzylaminopurine (BAP) for bud break. Maximum
numbers of shoots were induced on MS medium supplemented with 1.0 mg l-1 BAP. The cultures were
multiplied by continuous subculturing of shoots with mother explants on fresh MS medium with BAP
and Kinetin (Kin). Rooting was achieved on one fourth MS medium supplemented with 2.0 mg l-1
indole-3-butyric acid (IBA). The multiplied shoots were subjected to various concentrations of
different plant growth regulators and photoperiod regimes to induce flowering in vitro. The maximum
numbers of in vitro flowers were recorded from the shoots on full strength MS medium with 0.5 mg l-1
BAP and 0.1 mg l-1 indole-3-acetic acid (IAA) on 12/12 h/d photoperiod.
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