View/Open - ResearchSpace - University of KwaZulu-Natal
View/Open - ResearchSpace - University of KwaZulu-Natal
View/Open - ResearchSpace - University of KwaZulu-Natal
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Literature review<br />
the embryo (COPELAND, 1976). Stratification has also been known to decrease the<br />
time to germination and increase growth rate in other species (COPELAND, 1976).<br />
Stratification may also decrease the sensitivity to external conditions, so that a seed<br />
might, for example, germinate at a less suitable temperature (COPELAND, 1976).<br />
The germination rate may also be improved by exposing seeds to different day/night<br />
temperatures (COPELAND, 1976). In some cases embryonic dormancy may be<br />
broken by exposure to a certain light intensity, wavelength and/or photoperiod<br />
(COPELAND, 1976). In some cases dormancy caused by inhibitory chemicals within<br />
the embryo can be broken by gibberellic acid (COPELAND, 1976). Other chemicals<br />
which are known to break non-deep physiological dormancy include potassium<br />
nitrate, kinetin and ethylene. The effects <strong>of</strong> endogenous physical dormancy also<br />
diminishes as seed age increases (COPELAND, 1976).<br />
In the case <strong>of</strong> morphological dormancy, germination is prevented at the time <strong>of</strong><br />
maturity due to the morphological characteristics <strong>of</strong> the embryo. The embryo is<br />
underdeveloped or even undifferentiated at the time <strong>of</strong> dispersal and a period <strong>of</strong><br />
growth, known as after-ripening, is required before the seed can successfully<br />
germinate (COPELAND, 1976; BASKIN & BASKIN, 1998). Morphological dormancy<br />
occurs in seeds with rudimentary and linear embryos. Most <strong>of</strong> the interior <strong>of</strong> these<br />
seeds is occupied by endosperm and the embryo may only be 1% <strong>of</strong> the seed<br />
volume or less (BASKIN & BASKIN, 1998).<br />
Morphophysiological dormancy is essentially a combination <strong>of</strong> the two dormancy<br />
types. In this case the embryo must grow to a species-specific critical size and the<br />
physiological dormancy <strong>of</strong> the seed must occur before germination can take place<br />
(BASKIN & BASKIN, 1998).<br />
The primary reason for dormancy <strong>of</strong> seeds with exogenous physical dormancy is the<br />
impermeability <strong>of</strong> their seed or fruit coats to water (BASKIN & BASKIN, 1998). Seeds<br />
with physical dormancy frequently have a palisade layer <strong>of</strong> lignified cells in the testa<br />
or pericarp (BASKIN & BASKIN, 1998). The breakdown <strong>of</strong> such hard seed coats in<br />
the natural environment occurs through the gradual processes <strong>of</strong> hydration and<br />
dehydration, exposure to hot and cold temperatures, scorching by fire and<br />
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