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2.12 IN VITRO PROPAGATION OF GEOPHYTES<br />

Literature review<br />

ZIV (1997) defines geophytes as plants pereniating by underground storage organs.<br />

Geophytes are generally capable <strong>of</strong> developing tubers, corms or bulbs in vitro<br />

(STEINITZ & LILIEN-KIPNIS, 1989). Many ornamental geophytes are used for<br />

gardening, pot plant production, flowering pot plant production, cut flower production<br />

and the production <strong>of</strong> phytochemicals (ZIV, 1997).<br />

Plant biotechnology has provided geophyte production with clonal propagation, virus<br />

elimination, breeding and crop improvement through embryo rescue, in vitro<br />

fertilization, somaclonal variation, protoplast isolation and somatic hybridisation, and<br />

haploid production (ZIV, 1997). Genetic transformation is also aiding in geophyte<br />

development. Benefits include improving horticultural traits and induction <strong>of</strong> disease<br />

resistance (ZIV, 1997). Gene mapping and DNA fingerprinting are also additional<br />

developing areas (ZIV, 1997).<br />

Micropropagation has been achieved by enhanced axillary bud development,<br />

organogenesis and adventitious bud formation or by somatic embryogenesis (ZIV,<br />

1997). Explants used for propagation <strong>of</strong> bulbous, cormous and tuberous plants<br />

include the leaf lamina, petiole, mesophyll and epidermis (ZIV, 1997). Inflorescence<br />

peduncle, pedicel, tepals, petals, sepals, ovaries, anthers, ovules and embryos have<br />

also been used (ZIV, 1997). Other explants include the basal plate, scales, twin-<br />

scales and nodal and storage tissue <strong>of</strong> bulbs, corms and tubers (ZIV, 1997).<br />

The use <strong>of</strong> the underground pereniating organ as an explant source is <strong>of</strong>ten<br />

associated with heavy pathogen contamination (ZIV, 1997). This is a destructive use<br />

<strong>of</strong> the pereniating organ and eliminates the possibility <strong>of</strong> further vegetative or<br />

horticultural evaluation (ZIV, 1997). Different parts <strong>of</strong> the young flower and<br />

inflorescence stem can be cultured (ZIV, 1997). This is a source <strong>of</strong> pathogen-free<br />

totipotent explants (ZIV, 1997). Totipotency depends on the developmental stage at<br />

time <strong>of</strong> excision and position from which the explant was isolated (ZIV, 1997).<br />

Explants isolated from tissue positioned immediately next to the basal plate have a<br />

85

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