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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 8 (1985), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Fluorescein diacetate (FDA) staining (0.25% FDA for 10 min) was found to be a suitable technique for the rapid determination of orchid seed viability. Penetration of the dye through the testa varies between species, thus the test is ideally performed on isolated embryos. Direct FDA application to isolated embryos of seeds taken from dry storage, but after the surface had been sterilized, elicits a poor staining reaction. Incubation of the surface sterilized seeds in distilled water for 16 h, either at 6°C or at room temperature, prior to applying the test was found to overcome this problem. In the range of species studied, FDA staining accurately indicates seed viability when compared with germination of seeds on sterile nutrient media. Storage of dry Dactylorhiza fuchsii (Druce) Soó seed at an elevated temperature of 62°C indicated that, under such conditions of accelerated ageing, the FDA test accurately describes the rate of seed viability loss.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2048
    Keywords: Key words: Desiccation sensitivity ; Imbibition ; Oil body ; Oleosin ; Recalcitrant seed ; Seed storage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. In order to clarify further the physiological role of oleosins in seed development, we characterized the oil-body proteins of several oilseeds exhibiting a range of desiccation sensitivities from the recalcitrant (Theobroma cacao L., Quercus rubra L.), intermediate (Coffea arabica L., Azadirachta indica A. Juss.) and orthodox categories (Sterculia setigera Del., Brassica napus L.). The estimated ratio of putative oleosins to lipid in oil bodies of Q. rubra was less than 5% of the equivalent values for rapeseed oil bodies. No oleosin was detected in T. cacao oil bodies. In A. indica cotyledons, oil bodies contained very low amounts of putative oleosins. Oil bodies both from C. arabica and S. setigera exhibited a similar ratio of putative oleosins to lipid as found in rapeseed. In C. arabica seeds, the central domain of an oleosin was partially sequenced. Using a low temperature field-emission scanning electron microscope, the structural stability of oil bodies was investigated in seeds after drying, storage in cold conditions and rehydration. Despite the absence or relative dearth of oleosins in desiccation-sensitive, recalcitrant oilseeds, oil bodies remained relatively stable after slow or fast drying. In A. indica seeds exposed to a lethal cold storage treatment, no significant change in oil-body sizes was observed. In contrast, during imbibition of artificially dried seeds containing low amounts of putative oleosins, the oil bodies fused to form large droplets, resulting in the loss of cellular integrity. No damage to the oil bodies occurred in imbibed seeds of Q. rubra, C. arabica and S. setigera. Thus the rehydration phase appears to be detrimental to the stability of oil bodies when these are present in large amounts and are lacking oleosins. We therefore suggest that one of the functions of oleosins in oilseed development may be to stabilize oil bodies during seed imbibition prior to germination.
    Type of Medium: Electronic Resource
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