It has been shown that endosperm weakening, a necessary step in the light induction of germination in Datura ferox seeds, is related to the hydrolysis of cell wall mannose polysaccharides. It is demonstrated that the activities of two enzymes involved in mannan degradation (β-mannanase and β-mannosidase) are strongly promoted in the micropylar endosperm, after Pfr formation but long before radicle protrusion. An increase in enzyme activities occurred in dissected seed parts at similar rates to those in whole seeds, but only when at least a portion of the embryonic axis was present during incubation. De-embryonation of seed parts prevented the Pfr-induced increase in hydrolase activities. Exogenous GA3 promoted mannan-degrading enzyme activities both in the micropylar region of far red-treated whole seeds and those of isolated and deembryonated endosperm sections. The response to Pfr and GA3 was far more pronounced in the micropylar portion than in the rest of the endosperm. Pfr promotion of hydrolase activities and germination was blocked by paclobutrazol, an inhibitor of gibberellin synthesis. A close correlation was found between β-mannanase activity measured 45 h after Pfr formation and germination scored 24 h later. These results support the hypothesis that in D. ferox, endosperm softening is promoted by Pfr via the production in the embryonic axis of a factor, probably a gibberellin, which moves to the endosperm where it stimulates cell wall-mannan hydrolytic enzyme activities.

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Seed germination is often induced by a pulse of red light perceived by phytochrome and cancelled by a subsequent pulse of far-red light. When the pulse of red light is followed by several hours of darkness, a pulse of far-red light is no longer effective and prolonged far-red is necessary to block germination. The aim was to investigate whether the red light pulse and prolonged far-red light act on the same or different processes during germination of Datura ferox seeds. Forty-five hours after the inductive red light pulse, germination could not be blocked by one pulse or six hourly pulses of far-red light, but was significantly reduced by 6 h of continuous far-red light. The pulse of red light increased embryo growth potential and the activities of beta-mannanase and beta-mannosidase extracted from the micropylar region of the endosperm. Continuous far-red light had no effect on embryo growth potential or beta-mannosidase activity, but severely reduced the activity of beta-mannanase. The effect of far-red light had the features of a high-irradiance response of phytochrome. Both germination and beta-mannanase activity were restored by a pulse of red light given after the end of the continuous far-red treatment. It is concluded that the low-fluence response and the high-irradiance response modes of phytochrome have antagonistic effects on seed germination and that the control of beta-mannanase activity is one process where this antagonism is established.