K+ starvation inhibits water-stress-induced stomatal closure via ethylene synthesis in sunflower plants.

The effect of water stress on stomatal closure in sunflower plants has been found to be dependent on K(+) nutrient status. When plants with different internal K(+) content were subjected to a water-stress period, stomatal conductance was reduced more markedly in plants with an adequate K(+) supply than in K(+)-starved plants. K(+) starvation promoted the production of ethylene by detached leaves, as well as by the shoot of whole plants. Water stress had no significant effect on this synthesis. The effect on stomatal conductance of adding 5 microM cobalt (an ethylene synthesis inhibitor) to the growing medium of plants subjected to water stress was also dependent on their K(+) nutritional status: conductance was not significantly affected in normal K(+) plants whereas it was reduced in K(+)-starved plants. Cobalt had no harmful effects on growth, and did not alter the internal K(+) content in the plants. These results suggest that ethylene may play a role in the inhibiting effect of K(+) starvation on stomatal closure.

K+ deprivation induces xylem water and K+ transport in sunflower: evidence for a co-ordinated control.

The effect of K+ deprivation on water and K+ transport in roots was studied in sunflower plants. Deprivation was achieved in two different ways: by removing K+ from the growth medium for varying intervals; and by growing plants permanently in a low-K+ medium. Removal of K+ from the growth medium for a few hours prompted a significant increase in xylem sap exudation, associated with an increase in root hydraulic conductivity; however, it did not give rise to any significant change in plant K+ content, nor did it favour root K+ exudation. By contrast, prolonged K+ deprivation led to a decline in the internal K+ content and stimulated water and K+ transport in roots. Leaf application of K+ (Rb+) in plants grown permanently in a low-K+ medium inhibited the effect of K+ deprivation on root water and K+ transport, without significantly modifying the internal K+ content of the plants. This treatment had no effect on normal-K+ plants. These results suggest the existence of mechanisms enabling perception of plant K+ status and/or K+ availability in the medium, which trigger transduction processes governing the transport of water and K+ from the root to the shoot.

Na+ accumulation in root symplast of sunflower plants exposed to moderate salinity is transpiration-dependent.

Twenty-day-old sunflower plants (Helianthus annuus L. cv Sun-Gro 380) grown hydroponically under controlled conditions were used to study the effect of transpiration on Na(+) compartmentalization in roots. The plants were exposed to low Na(+) concentrations (25 mM NaCl) and different environmental humidity conditions over a short time period (8.5 h). Under these conditions, Na(+) was accumulated primarily in the root, but only the Na(+) accumulated in the root symplast was dependent on transpiration, while the Na(+) accumulated in both the shoot and the root apoplast exhibited a low transpiration dependence. Moreover, Na(+) content in the root apoplast was reached quickly (0.25 h) and increased little with time. These results suggest that, in sunflower plants under moderate salinity conditions, Na(+) uptake in the root symplast is mediated by a transport system whose activity is enhanced by transpiration.

K(+) starvation inhibits water-stress-induced stomatal closure.

The effect of potassium starvation on stomatal conductance was studied in olive trees and sunflower plants, two major crops with greatly differing botanical characteristics. In both species, K(+) starvation inhibited water-stress-induced stomatal closure. In olive trees, potassium starvation favoured stomatal conductance and transpiration, as well as inhibiting shoot growth, in the three cultivars studied: 'Lechín de Granada', 'Arbequina' and 'Chetoui'. However, 'Lechín de Granada' - generally considered more drought-tolerant than 'Arbequina' and 'Chetoui' - proved less susceptible to potassium starvation. Results for olive trees also suggest genetic variability in olive cultivars in relation to potassium requirements for stem growth and the regulation of water transpiration. The results obtained suggest that inhibition of the stomatal closure mechanism produced by moderate potassium starvation is a widespread plant physiological disorder, and may be the cause of tissue dehydration in many water-stressed crops.

Na+ accumulation in shoot is related to water transport in K+-starved sunflower plants but not in plants with a normal K+ status.

Sunflower plants (Helianthus annuus L. cv Sun-Gro 380) grown in nutrient solutions with different K+ levels were used to study the effect of potassium status on water uptake, Na+ uptake and Na+ accumulation in the shoot. Changes in nutrient potassium levels induced evident differences in internal potassium content. When both low and normal-K+ plants were exposed to 22 degrees C and salinity conditions (25 or 50 mM NaCl) during a short time period (9h), water uptake in low-K+ plants was greater than in normal-K+ plants. In addition, K+ starvation favoured the Na+ uptake and the Na+ accumulation both in the root and in the shoot. When the plants were exposed to heat stress by a sharp increase of the temperature to 32 degrees C during the same period of time, the stimulating effect of K+ starvation on the water uptake was even greater. The high temperature increased Na+ uptake in both types of plants, but the Na+ accumulation in the shoot was only favoured in low-K+ plants. The results suggest that Na+ accumulation in the shoot is more dependent on the water uptake in low-K+ plants than in normal-K+ plants, and this effect could explain the greatest susceptibility to the salinity in K+-starved plants under high transpiration conditions, which are typical in dry climates.