Modelling water flow, nitrogen transport and root uptake including physical non-equilibrium and optimization of the root water potential

1991 ◽  
Vol 27 (2-3) ◽  
pp. 215-231 ◽  
Author(s):  
F. Lafolie
1985 ◽  
Vol 15 (1) ◽  
pp. 185-188 ◽  
Author(s):  
T. M. Ballard ◽  
M. G. Dosskey

Needle water potential in western and mountain hemlock falls as the soil dries, but under our experimental conditions, it remained stable in Douglas-fir. Resistance to water flow from soil to foliage is higher for the hemlocks and increases more steeply as the soil dries. These findings physically account for the observation that water uptake is reduced relatively more for the hemlocks than for Douglas-fir, as soil water potential declines.


1986 ◽  
Vol 16 (1) ◽  
pp. 98-102 ◽  
Author(s):  
Takefumi Ikeda ◽  
Tamio Suzaki

The reduction in water potential of cuttings after planting in water closely was related to an increase in resistance to water flow in the xylem. From observations of water-conducting tissues using a scanning electron microscope, the increase in resistance to water flow of cuttings was caused by blockage of vessel lumens with tyloses for Populuscarolinensis and aspiration of bordered pits for Cryptomeriajaponica. Water status of cuttings decreased with time after planting and was maintained at a low level by water absorption through bark. After rooting, the total resistance to water flow decreased and the water status of cuttings increased.


1975 ◽  
Vol 55 (4) ◽  
pp. 941-948 ◽  
Author(s):  
P. A. DUBÉ ◽  
K. R. STEVENSON ◽  
G. W. THURTELL ◽  
H. H. NEUMANN

Determinations of plant resistance to water flow from measurements of leaf water potential at steady transpiration rates were made on different lines of corn (Zea mays L.). Two inbreds, Q188, a wilting mutant, and DR1, an inbred line shown to have at least some heat and drought tolerance under field conditions, were compared to a commercial single-cross hybrid, United 106. The purpose of the experiment was to isolate the cause of the wilting characteristic of Q188. A linear relationship was found between leaf water potential and transpiration rate for all lines. No water potential gradients were found at zero transpiration. Low total plant resistances were observed in United 106 and DR1, with the major resistance being in the root system in both genotypes. Although the resistance to water movement through the roots and lower stalk in Q188 did not appear to differ from those of the other lines, a much larger resistance was found in the upper stalk of Q188; resistance to water movement through the lower stalk (up to node 5) decreased as the plants matured from 55 to 70 days of age but no comparable changes occurred in the upper portions of the stem. In vivo detection of the xylem vessels with staining techniques confirmed the observed differences in resistances.


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