The water relations of hemlock (Tsuga canadensis). IV. The dependence of the balance pressure on temperature as measured by the pressure-bomb technique

1974 ◽  
Vol 52 (5) ◽  
pp. 973-978 ◽  
Author(s):  
M. T. Tyree ◽  
J. Dainty ◽  
D. M. Hunter

The temperature dependence of the balance pressure is reported for shoots of Tsuga canadensis at constant volume, i.e., when water is neither added to nor removed from the shoot. Since the balance pressure closely equals minus the water potential, the temperature dependence of the balance pressure should reflect the combined temperature dependence of the osmotic and turgor pressures. Both the osmotic and the turgor pressures decline with decreasing temperature; frequently the turgor pressure declines 2 to 3 times more rapidly than the osmotic pressure, causing the balance pressure to rise with decreasing temperature. Only when the turgor pressure is zero (only beyond incipient plasmolysis) does the temperature dependence of the balance pressure closely follow the temperature dependence of the osmotic pressure; this occurs when the balance pressure equals or exceeds 24 bars.

1978 ◽  
Vol 56 (17) ◽  
pp. 2153-2161 ◽  
Author(s):  
M. T. Tyree ◽  
M. E. MacGregor ◽  
A. Petrov ◽  
M. I. Upenieks

The pressure bomb is being used to a much greater extent to measure some tissue – water relations parameters such as osmotic pressure, turgor pressure, and cell wall elasticity. Recently, Richards has developed a faster pressure-bomb method of obtaining these and other parameters than the method used by Hammel and modified by us. In this paper, we compare the two methods and conclude that Richards’ method should not be used when accuracy is deemed important. The Richards method usually overestimates osmotic pressure by 0.2 MPa (= 2 bars) and sometimes by 0.8 MPa (= 8 bars).


1978 ◽  
Vol 56 (6) ◽  
pp. 635-647 ◽  
Author(s):  
M. T. Tyree ◽  
Y. N. S. Cheung ◽  
M. E. MacGregor ◽  
A. J. B. Talbot

The Scholander–Hammel pressure bomb has been used to measure ontogenetic and seasonal changes in π0 (the osmotic pressure of the symplasm at zero water potential), πp (the osmotic pressure of the symplasm at ‘incipient plasmolysis’), εmax (the bulk elastic modulus near maximum turgor), and a number of other water relations parameters in single leaves of Acer saccharum and several species of Populus and in shoots of Tsuga canadensis and Picea abies. In newly emerged leaves of Acer, Populus, and Picea, π0, πp, and εmax are all small but rise rapidly with leaf development. These parameters stabilize at a maximum value or slowly increase with progress in season. In Acer, εmax declines shortly before senescence. In developing leaves, the water content reaches a maximum before the soluble solutes; this accounts for the low values of π0 and πp.In Tsuga π0 cycles through an annual maximum in winter and a minimum in summer. These changes may correlate with frost hardiness.


1973 ◽  
Vol 51 (8) ◽  
pp. 1471-1480 ◽  
Author(s):  
M. T. Tyree ◽  
J. Dainty ◽  
M. Benis

Theoretical and experimental aspects of the equilibrium water relations of excised hemlock (Tsuga canadensis) shoots are examined. The equilibrium water relations of hemlock were determined by using the pressure-bomb technique on shoots 15 to 40 g in fresh weight. At or near full turgor the osmotic pressure of the cells averages 16.5 + 0.4 bars. The fraction of the total water content of hemlock shoots residing in the living cells is 0.77 + 0.04. When hemlock shoots are near full turgor the balancing pressure will change linearly with the volume expressed provided the volume changes represent less than [Formula: see text] of the total shoot water content.


1989 ◽  
Vol 16 (6) ◽  
pp. 517 ◽  
Author(s):  
SD Tyerman ◽  
P Oats ◽  
J Gibbs ◽  
M Dracup ◽  
H Greenway

Nicotiana tabacum plants were grown in solution culture with salinity treatments of 1, 100 and 200 mol m-3 [NaCl], in Hoagland solution. After several weeks, solute concentrations and osmotic pressure of cell sap from the roots were measured. Increases in cellular [Na+] and [Cl-] and a smaller reduction in [K+] accounted for the difference in sap osmotic pressure between the 200 mol m-3 and 1 mol m-3 treatments. Turgor pressure (P) of fully expanded cortex cells measured with the pressure probe were 0.48 MPa in 1 mol m-3, 0.24 MPa in 100 mol m-3, 0.20 MPa in 200 mol m-3, and these values agreed with those calculated by difference between internal and external osmotic pressure. Low values of volumetric elastic modulus (ε), ranging from 1.2 MPa to 3.0 MPa at P = 0.42 MPa were obtained, which accounted for long equilibration times to changes in water potential. There was no effect of high salinities on ε after accounting for the fact that ε was a function of P and neither was there an effect on hydraulic conductivity (Lp), which ranged between 1.9 × 10-8 and 24.1 × 10-8 m s-1 Mpa-1. At 200 mol m-3 [NaCl]o, and to a lesser degree at 100 mol m-3 [NaCl]o, root hairs became deformed to resemble spherical bladders (mean diameter = 88 �m) which displayed similar P and water relations to other epidermal cells and cortex cells. In other experiments the response to a sudden reduction in [NaCl], from 200 to 1 mol m-3 was studied. P of cortex cells first rapidly increased from about 0.15 MPa to 0.53 MPa and then slowly declined with a half time of about 35 min to a new steady state of 0.3 MPa. This level was maintained in intact roots for at least 48 h. The rate of the initial increase in P is limited by water flow into the cells while the slow decline is limited by solute efflux from the cells with water following osmotically. The efflux was mainly in response to reduced external osmotic pressure rather than [NaCl]o. Efflux of Na+, K+ and Cl- accounted for the decrease in internal osmotic pressure but it is possible that the membrane also became more permeable to sugars. With the exception of bladder hairs, the overall integrity of the cell membrane was maintained since Lp did not increase and P declined smoothly to the new level with no evidence of rupture and resealing of the membrane. It is argued that the loss of solutes after the step down in external osmotic pressure consists of turgor or volume regulation in which solute permeability increases steeply as turgor or volume goes above a threshold.


1963 ◽  
Vol 47 (1) ◽  
pp. 83-101 ◽  
Author(s):  
Peter M. Ray ◽  
Albert W. Ruesink

Efforts were made to estimate the water potential difference that is required, between rapidly growing oat coleoptile cylinders and dilute medium, to support the rate of water uptake involved in elongation, (a) by the traditional method of determining the concentration of mannitol in which the tissue neither gains nor loses water, and (b) by measuring the rates of osmotic exchanges induced by treating the tissue with different hypotonic mannitol concentrations. Both methods indicated large water potential differences (3 to 10 atm), in some cases approaching the osmotic pressure of the cells. However, indication was obtained that the rates of osmotic exchanges induced by mannitol solutions, and presumably also the equilibrium response sought in (a), are governed by the rate of diffusional exchange of mannitol with the free space rather than by the permeability of the tissue to water. Osmotic swelling of the tissue measured by immersing it in water after its turgor pressure had been reduced by evaporation, was at least two to four times more rapid than when mannitol was involved. The permeability to water estimated by the evaporation-immersion method indicated that rapidly elongating cylinders have water potentials between -0.8 and -2.5 atm, or between 10 and 25 per cent of their osmotic pressure.


1975 ◽  
Vol 53 (13) ◽  
pp. 1342-1346 ◽  
Author(s):  
Y. N. S. Cheung ◽  
M. T. Tyree ◽  
J. Dainty

The physical implications of the various parameters obtained from a pressure-bomb study are explored and related to their possible ecological significance. Our analysis suggests that the original bulk osmotic pressure, the bulk osmotic pressure at incipient plasmolysis, and cell wall elasticity are closely associated with the extent to which a leaf can osmoregulate or conserve water within a certain range of water potential change in the environment and might therefore have certain adaptive value. The pressure–volume relation could be applied to predict changes in leaf water potential at various degrees of water loss in the field. The values of these various parameters were obtained from a pressure-bomb study on single leaves from a wide variety of species. The use of data from single leaves as compared with whole shoots is discussed.


1975 ◽  
Vol 53 (8) ◽  
pp. 784-788 ◽  
Author(s):  
A. J. B. Talbot ◽  
M. T. Tyree ◽  
J. Dainty

Psychrometric measurements of the water potentials of leaves of Tsuga canadensis (L.) Carr. and Picea abies L. are compared with the water potentials of the shoots from which they came as measured by the pressure-bomb technique. Agreement between the two techniques is good when whole leaves are used in the psychrometer chamber, but deviations occur when bisected leaves are used in which the wound area to tissue volume is very small (1 to 2 cm2/cm3 of leaf tissue). Psychrometer determinations of water potential of these detached leaves are much more sensitive to cutting than in other species, e.g., sunflower and pepper (2). A more reliable means of measuring turgor and osmotic pressures in leaves is proposed.


1973 ◽  
Vol 51 (8) ◽  
pp. 1481-1489 ◽  
Author(s):  
M. T. Tyree ◽  
J. Dainty

We present a theoretical analysis of the events that occur while a plant enclosed in a pressure bomb evolves from one equilibrium balancing pressure to another. The initial rate of efflux from any one cell in response to a pressure increment of ΔP equals (ALp)i ΔP, where (ALp)i is the surface area times hydraulic conductivity of the cell's semipermeable membrane(s). If the volume changes and pressure increment are small, the cell will approach equilibrium exponentially. The half time of the exponential process is governed by (ALp)iki, where ki is the cell constant (= the combined rate of change of osmotic and turgor pressure with the volume expressed from the cell). Experimental studies of the kinetics of water exchange between the symplast and apoplast of hemock (Tsuga canadensis) shoots in a pressure bomb reveal that the cells collectively behave as though they fall into three distinct populations which approach equilibrium with different half times.


1981 ◽  
Vol 8 (3) ◽  
pp. 329 ◽  
Author(s):  
WJS Downton

The water relations of laticifers in N. oleander were examined for plants growing in Death Valley, California, USA. Osmotic potential of laticifers in well watered plants paralleled the daily changes in leaf water potential. The turgor pressure of laticifers was usually less than bulk leaf turgor. Laticifer turgor was maintained in the absence of positive leaf turgor in severely water stressed plants (Ψw ͭ6 -7.0 MPa) and latex exuded when leaves were cut. The recovery in water status of leaves and laticifers following watering of the plants is described. Laboratory measurements confirmed that laticifer turgor differed from bulk leaf turgor and that it was maintained over a range of water potentials. These observations may have relevance for some of the latex-bearing plants currently being considered as future hydrocarbon sources.


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