Physiological dormancy of scarified seeds of Townsville stylo (Stylosanthes humilis HBK) was released by acidic aluminium (Al3+) solution. Antiethylenic substances inhibited germination of low-pH-stimulated dormant seeds, with a correspondingly low ethylene production and low activity of 1-aminocyclopropane-1-carboxylate (ACC) oxidase in seeds. On the other hand, antiethylenic substances did not decrease the germination of Al3+-stimulated seeds, but ACC oxidase activity and ethylene production by the seeds was decreased to a large extent. These data provide evidence that dormancy breakage by Al3+ differs from that caused by low pH and is not associated with ethylene production. Similarly to Al3+ action, methyl viologen (MV), a reactive oxygen species-generating compound, broke dormancy of Townsville stylo seeds. Sodium selenate and N-acetyl cysteine, antioxidant compounds, largely decreased germination of MV- and Al3+-stimulated dormant seeds. Altogether these data point to oxidative radicals constituting key molecules in the chain of events triggered by Al3+ leading to dormancy breakage.

The soluble selenium (Se) compounds selenic acid, selenious acid, selenium dioxide, selenium tetrachloride, selenomethionine, selenourea, sodium selenate and sodium selenite broke the dormancy of scarified seeds of Townsville stylo (Stylosanthes humilis HBK). Given the chemical diversity of all these molecules, it could be deduced that Se may act as a dormancy-breaking agent of Townsville stylo seeds. Se-stimulated seeds produced great amounts of both ethylene and 1-aminocyclopropane-1-carboxylic acid, which correlated with the process of germination. As specific inhibitors of ethylene biosynthesis and action largely depressed this Se-stimulated germination, it was concluded that Se broke dormancy by triggering ethylene production by the seeds.

Physiological dormancy of scarified seeds of Townsville stylo (Stylosanthes humilis H.B.K.) is broken by ethylene. When the biosynthesis of this gas was impaired by 2-aminoethoxyvinylglycine (AVG) plus Co2+, the response to ethylene at very low concentrations was appreciable in non-dormant seeds and nil in the dormant ones. Complete inhibition of germination of non-dormant seeds occurred only when they were treated with AVG plus Co2+ under an ethylene-free atmosphere, a condition in which no trace of the gas in the atmosphere of Erlenmeyer flasks could be detected. Injection of ethylene into that system triggered germination of both dormant and non-dormant seeds, demonstrating a requirement for the gas. Non-dormant seeds were at least 50-fold more sensitive to ethylene than the dormant ones. Perception of ethylene occurred within a very short time (at most 15 min), since exposure of both dormant and non-dormant seeds to the gas, at a steeply declining concentration, sufficed to cause substantial germination.