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A review of dipterocarps - Center for International Forestry Research

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Seed Physiology 63<br />

Table 4. Lowest-safe moisture content values (wet weight basis) <strong>for</strong> mature seeds*.<br />

Species Source LSMC (%)<br />

Dipterocarpus alatus** Tompsett (unpub.) 25<br />

Shorea siamensis Tompsett (unpub.) 51***<br />

Shorea singkawang Yap (1986) 55<br />

Shorea xanthophylla Tompsett (unpub.) >41***<br />

Stemonoporus canaliculatus Tompsett (unpub.) 43***<br />

Vatica umbonata Mahdi (1987) 74****<br />

*: no slopes and intercepts available <strong>for</strong> these species;<br />

**: seed is OLDA (orthodox with limited desiccation ability);<br />

changes accompanying loss <strong>of</strong> viability <strong>of</strong> S. robusta<br />

have also been reported (Nautiyal et al. 1985).<br />

Some authors have confused the effects <strong>of</strong><br />

desiccation itself with the effects <strong>of</strong> ageing; in order to<br />

determine the effects <strong>of</strong> ageing, moisture contents<br />

should be kept constant. However, in studies by Song et<br />

al. (1983) on Hopea hainanensis it is clear that<br />

desiccation effects per se were being examined. At 36%<br />

moisture content the ultrastructure was intact, but on<br />

desiccation to 26% moisture content, which severely<br />

reduces germination percentage, various changes were<br />

observed. Vesicles appeared in the cytoplasm, vacuolar<br />

membranes ruptured and cell contents became less<br />

distinct. Cell walls and cytoplasm became separated and<br />

nuclear membranes could not be distinguished from the<br />

nucleolus. These changes illustrate a general<br />

deterioration <strong>of</strong> cellular structure rather than an effect<br />

confined to the cell membrane. In a further study (Song<br />

et al. 1986), desiccation to 31% was shown to disturb<br />

the ribosomes and endoplasmic reticulum, but these<br />

changes were reversed on re-hydration.<br />

More recently, Krishan Chaitanya and Naithani<br />

(1994) measured changes in superoxide, lipid<br />

***: based on at least 25 seeds per germination;<br />

****: unusually high value.<br />

peroxidation and superoxide dismutase <strong>for</strong> seeds <strong>of</strong> S.<br />

robusta during desiccation. They concluded that the loss<br />

<strong>of</strong> viability observed may be caused by the cumulative<br />

effect <strong>of</strong> peroxidation products <strong>of</strong> polyunsaturated fatty<br />

acids and peroxidation <strong>of</strong> the membrane lipids.<br />

Storage Physiology<br />

Some aspects <strong>of</strong> seed storage are considered elsewhere:<br />

practical aspects, including the effects <strong>of</strong> gases, are<br />

discussed in Chapter 4; chilling physiology is considered<br />

above under germination effects. Topics discussed below<br />

include the following: best recorded storage periods; use<br />

<strong>of</strong> viability constants; the significance <strong>of</strong> oil contents;<br />

some aspects <strong>of</strong> tissue culture; and various associations<br />

with storage physiology.<br />

Best storage records<br />

An up-to-date summary <strong>of</strong> best storage records is given<br />

in Table 5. These records should not be confused with<br />

practical recommendations; if the recommended storage<br />

conditions were employed, longer storage would be<br />

expected in many cases. The best record <strong>for</strong> an OLDA<br />

species is 2829 days <strong>for</strong> Dipterocarpus alatus and the

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