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Literature review<br />

organ is then produced on this medium. Successful determination is partially<br />

dependent on the chemical and physical environment to which they have been<br />

exposed. The result <strong>of</strong> failure <strong>of</strong> explant tissues to express totipotency is a failure <strong>of</strong><br />

the explant tissues to achieve the state <strong>of</strong> competence for induction. This makes<br />

investigation <strong>of</strong> the effects <strong>of</strong> physical and chemical parameters difficult. The use <strong>of</strong><br />

biochemical or genetic markers that can clearly indicate the developmental<br />

disposition <strong>of</strong> the primary explant tissue have not yet been discovered (SCHWARTZ<br />

et al., 2004).<br />

In the next phase the morphological differentiation and development <strong>of</strong> the nascent<br />

organ occurs (SCHWARTZ et al., 2004). Organ initiation involves a rapid shift in<br />

polarity followed by a smoothing <strong>of</strong> this shift into a radially symmetrical organization<br />

and the concurrent growth along the new axis to form a characteristic bulge<br />

(SCHWARTZ et al., 2004). There is not an absolute certainty as to which tissues are<br />

involved and the number <strong>of</strong> cells involved in meristem initiation (SCHWARTZ et al.,<br />

2004).<br />

The initiation <strong>of</strong> adventitious roots occurs in four stages (SCHWARTZ et al., 2004). A<br />

meristematic locus is first formed by the dedifferentiation <strong>of</strong> a stem or other cells.<br />

These cells then multiply to form a spherical cluster. Further cell multiplication occurs<br />

with the initiation <strong>of</strong> planar divisions to form a recognizable bilateral root meristem.<br />

Lastly, the cells located in the basal part <strong>of</strong> the developing meristem elongate,<br />

resulting in the eventual emergence <strong>of</strong> the newly formed root (SCHWARTZ et al.,<br />

2004). The production <strong>of</strong> a functional adventitious root system depends on the<br />

selection <strong>of</strong> a microcutting <strong>of</strong> the appropriate developmental stage and the ability <strong>of</strong><br />

the in vitro environment to initiate the sequence <strong>of</strong> events described above<br />

(SCHWARTZ et al., 2004).<br />

2.9.8 Somatic embryogenesis<br />

In plants, morphologically and functionally correct nonzygotic embryos can arise from<br />

an array <strong>of</strong> cell and tissue types at a number <strong>of</strong> different points within both the<br />

gametophytic and sporophytic phases <strong>of</strong> the plant life cycle (GRAY, 2005). Somatic<br />

(or asexual) embryogenesis involves the formation <strong>of</strong> embryo-like structures, which<br />

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