Phosphorus-induced Leaf Abscission in Olive and Citrus Explants

Previous studies, in which the role of phosphorus in abscission of olive leaves was examined in the presence of ethylene biosynthesis inhibitors, have suggested that phosphorus induces abscission directly, without involvement of ethylene. In the present study, this possibility was further explored by comparing the effects of an ethylene biosynthesis inhibitor, aminoethoxyvinylglycine (AVG), and an ethylene action inhibitor, 2,5-norbornadiene (NBD), in olive [Olea europaea (L) cv. Manzanillo] and citrus [Citrus sinensis (L.) Osbeck cv. Shamouti]. In olive, leaf abscission was always induced in the presence of KH2PO4, with or without AVG and NBD (alone or in combination), but was more pronounced when KH2PO4 was applied alone. In citrus, the effect of KH2PO4 alone on the induction of leaf abscission and ethylene production was much stronger than that observed in olive. However, in the presence of NBD, KH2PO4 did not induce leaf abscission in citrus during the first 60 hr. Similar results were obtained when NBD was replaced by AVG, but, in this case, abscission was inhibited for only 48 hr. In both cases, ethylene was detected after the inhibitory period had ended. The results obtained with citrus indicate that the observed effect of KH2PO4 on the ethylene-independent induction of leaf abscission in olive is not a general phenomenon and may differ in different species.

Effects of membrane potential on mechanical activation in skeletal muscle.

The effect of subthreshold depolarization on mechanical threshold was investigated in tetrodotoxin-poisoned mammalian and amphibian skeletal muscle fibers using a two-microelectrode voltage-clamp technique. Mechanical threshold was determined with a 2-ms test pulse. The immediate effect of depolarization was inhibition of the mechanical system. The consequent increase in the test pulse threshold was linearly related to the size of the depolarization and there was, on the average, a 10% increase in threshold for a 10-mV depolarization in mammalian fibers. The duration of the inhibitory period was also related to the size of the depolarization. Inhibition was interrupted by the onset of activation (seen as a reduction in the test pulse threshold), and in rat soleus fibers this occurred within 100 ms with a 20-mV depolarization, inhibition decayed within 10 ms. The decay of activation after brief conditioning pulses was initially rapid (on the average, the test pulse threshold recovered to 80% of its control value within 1 ms) and then slow (full recovery took 100-500 ms). After long conditioning pulses, activation often decayed into a period of inhibition. When depolarization (of 20 mV or more) was maintained for several seconds, the fibers became inactivated. Rat extensor digitorum longus and sternomastoid fibers were strongly inactivated by depolarization to -40 mV and the test pulse to +40 mV did not cause contraction.

Transient Responses of Rabbit Retinal Ganglion Cells to Photic and Electrical Stimuli

SUMMARY:The relationships between the center and the surround of the receptive field of the rabbit retinal ganglion cell were investigated. This was done by coupling localized light spots and electrical activation of the retina and by analyzing the time of the excitatory and inhibitory periods. The responsiveness to the electrical transretinal pulse revealed a) that ON stimulation in OFF-center cells and OFF stimulation in ON-center cells, elicited a primary period of inhibition with a short latency; b) the long latency response of surround stimulation was not preceded by an inhibitory period unless the center was simultaneously stimulated in the same direction; c) a transient response to a stationary spot of light is followed by a period of inhibition. These results are discussed in relation to the known cellular retinal networks.