Effects of olive root warming on potassium transport and plant growth.

Young olive (Olea europaea L.) plants generated from seed were grown in liquid hydroponic medium exposing the roots system for 33days or 24h to high temperature (37°C) while the aerial part to 25°C aiming to determine the prolonged and immediate effects of root warming on K+(Rb+) transport in the root and consequently on plant growth. The exposition of the root system to 37°C for 24h inhibited K+ (Rb+) transport from root to shoot having no effect on its uptake. However, when the root system was exposed permanently to 37°C both the K+ (Rb+) uptake and translocation to the aerial part were inhibited as well as the growth in all plants organs. The ability of the root system to recover K+ (Rb+) uptake and transport capacity after being exposed to high temperature was also evaluated. Plants grown in a root medium at 37°C for 31days were transferred to another at 25°C for 48 or 96h. The recovery of K+ (Rb+) root transport capacity after high root temperature was slow. Any signal of recovery was observed after 48h without stress: both potassium root uptake and subsequent transport to above organs were inhibited yet. Whereas 96h without stress led to restore potassium upward transport capacity although the uptake was partially inhibited yet. The results obtained in this study have shown that the root system of young olive plants is very sensitive to high temperature related to root potassium transport and growth of the plant. Taking into account the two processes involved in root potassium transport, the discharge of K+ to the xylem vessels was more affected than the uptake at the initial phase of high root temperature stress. However, it was the first process to be re-established during recovery. All this could explain the symptoms frequently observed in olive orchards when dry and high temperature spells occur: a reduction in shoots growth and leaves with low levels of potassium contents and dehydration symptoms.

Effect of moderate high temperature on the vegetative growth and potassium allocation in olive plants.

There is little information about the prolonged effect of a moderately high temperature on the growth of olive (Olea europaea L.). It has been suggested that when the temperature of the air rises above 35°C the shoot growth of olive is inhibited while there is any reference on how growth is affected when the soil is warmed. In order to examine these effects, mist-cuttings and young plants generated from seeds were grown under moderate high temperature (37°C) for 64 and 42days respectively. In our study, plant dry matter accumulation was reduced when the temperature of both the air and the root medium was moderately high. However, when the temperature of the root medium was 25°C, the inhibitory effect of air high temperature on plant growth was not observed. The exposure of both the aerial part and the root to moderate high temperature also reduced the accumulation of K+ in the stem and the root, the water use efficiency and leaf relative water content. However, when only the aerial part was exposed to moderate high temperature, the accumulation of K+ in the stem, the water use efficiency and leaf relative water content were not modified. The results from this study suggest that the olive is very efficient in regulating the water and potassium transport through the plant when only the atmosphere surrounding the aerial part is warmed up. However, an increase in the soil temperature decrease root K+ uptake and its transport to the aerial parts resulting in a reduction in shoot water status and growth.

Co-regulation of water and K(+) transport in sunflower plants during water stress recovery.

16-day-old sunflower (Helianthus annuus L.) plants were subjected to deficit irrigation for 12 days. Following this period, plants were rehydrated for 2 days to study plant responses to post-stress recovery. The moderate water stress treatment applied reduced growth in all plant organs and the accumulation of K(+) in the shoot. After the rehydration period, the stem recovered its growth and reached a similar length to the control, an effect which was not observed in either root or leaves. Moreover, plant rehydration after water stress favored the accumulation of K(+) in the apical zone of the stem and expanding leaves. In the roots of plants under water stress, watering to field capacity, once the plants were de- topped, rapidly favored K(+) and water transport in the excised roots. This quick and short-lived response was not observed in roots of plants recovered from water stress for 2 days. These results suggest that the recovery of plant growth after water stress is related to coordinated water and K(+) transport from the root to the apical zone of the ​​stem and expanding leaves. This stimulation of K(+) transport in the root and its accumulation in the cells of the growing zones of the ​​stem must be one of the first responses induced in the plant during water stress recovery.

Rhizospheric bacteria alleviate salt-produced stress in sunflower.

The effect of isolate Pseudomonas fluorescens biotype F and P. fluorescens CECT 378(T) inoculation on fresh weight and ions accumulation was studied in sunflower plants grown in sand:peat substrate with addition of 100mM NaCl. The inoculation resulted in an increase in fresh weight of more than 10% in salt treatments and in an accumulation of less Na(+) and more K(+) in plant tissues in all cases. The bacterial inoculants favoured the K(+)/Na(+) ratio in all plant parts and in the case of the isolate CECT 378(T) conducted to 66% increment in leaves, 34% in stems and 16% in roots, while the effect of isolate inoculation was (only) more evident in leaves and stems with 30% and 26%, respectively. Both strains were found to produce indoleacetic acid and siderophores in in-vitro tests, thus the production of indoles was highly dependent on the exogenous tryptophan in the medium. The results suggest that salt stress in sunflower plants was alleviated partially by the inoculation with strains that produce indoles and siderophores, having also a positive effect on the K(+)/Na(+) ratio in the shoot. Moreover, those plants were characterized with better-developed roots.

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.

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.