Development of a sensor suite to determine plant water potential

2010 ◽  
Author(s):  
Vasu Udompetaikul ◽  
Shrini K Upadhyaya ◽  
David C Slaughter ◽  
Bruce D Lampinen
Keyword(s):  
Water Potential ◽  
Plant Water ◽  
Plant Water Potential ◽  
Sensor Suite

Water relations of winter wheat. 5. The root system and osmotic adjustment in relation to crop evaporation

1984 ◽  
Vol 102 (2) ◽  
pp. 415-425 ◽  
Author(s):  
M. McGowan ◽  
P. Blanch ◽  
P. J. Gregory ◽  
D. Haycock
Keyword(s):  
Winter Wheat ◽  
Water Potential ◽  
Root System ◽  
Soil Water ◽  
Osmotic Adjustment ◽  
Stomatal Closure ◽  
Soil Water Potential ◽  
Plant Water ◽  
Potential Evaporation ◽  
Plant Water Potential

SummaryShoot and root growth and associated leaf and soil water potential relations were compared in three consecutive crops of winter wheat grown in the same field. Despite a profuse root system the crop grown in the second drought year (1976) failed to dry the soil as throughly as the crops in 1975 and 1977. Measurements of plant water potential showed that the restricted utilization of soil water reserves by this crop was associated with failure to make any significant osmotic adjustment, leading to premature loss of leaf turgor and stomatal closure. The implications of these results for models to estimate actual crop evaporation from values of potential evaporation are discussed.

Internal Water Balance of Brigalow (Acacia harpophylla F. Muell.) Under Natural Conditions

1975 ◽  
Vol 2 (4) ◽  
pp. 489 ◽  
Author(s):  
BR Tunstall ◽  
DJ Connor
Keyword(s):  
Water Potential ◽  
Water Status ◽  
Carbon Uptake ◽  
Diurnal Changes ◽  
Plant Water ◽  
Litter Fall ◽  
Tissue Water ◽  
Diffusive Resistance ◽  
Plant Water Potential ◽  
Water Contents

On one day each month over a period of 2½ years, diurnal measurements of plant water status, leaf diffusive resistance, carbon uptake, irradiance, ambient temperature and humidity were made in a brigalow community. Diurnal changes in leaf diffusive resistance, osmotic potential, plant water potential, and carbon uptake are shown to follow general patterns and the changes in plant water potential were related to the dawn value of plant water potential. The data suggest the development of negative turgor in brigalow and demonstrate the capacity of the plant to maintain high tissue water contents at low water potentials. Measurements of shoot extension and litter fall showed that litter fall occurred principally following shoot extension.

scholarly journals Plant Water Potential for Shrubs in Argentina

1987 ◽  
Vol 40 (1) ◽  
pp. 6 ◽  
Author(s):  
Daniel V. Pelaez ◽  
Roberto M. Boo
Keyword(s):  
Water Potential ◽  
Plant Water ◽  
Plant Water Potential

A dynamic simulation of loblolly pine (Pinustaeda L.) seedling establishment based upon carbon and water balances

1988 ◽  
Vol 18 (7) ◽  
pp. 833-850 ◽  
Author(s):  
John I. Blake ◽  
Gerrit Hoogenboom
Keyword(s):  
Drought Stress ◽  
Water Potential ◽  
Loblolly Pine ◽  
Carbon Allocation ◽  
Weather Data ◽  
Soluble Carbohydrate ◽  
Plant Water ◽  
Short Term ◽  
Evaporative Demand ◽  
Plant Water Potential

A generalized simulation model, ROOTSIMU, which utilizes dynamic carbon and water balance algorithms, was modified to simulate loblolly pine (Pinustaeda L.) seedling growth and water uptake for a 100-day transplant period. The modifications included an allowance for time-dependent changes in photosynthesis and carbon allocation. Heat sums were used to control the initiation of growth. Additional compartments were added to separate the physiological functions of suberized and nonsuberized roots and secondary woody tissues. Values used to initialize the model were largely derived from the published literature. The predicted results of a simulation run using 1985 and 1986 weather data are reported. Changes in simulated plant water potential were closely related to periods of rainfall or high evaporative demand. Midday values were occasionally less than −7 MPa when evaporative demand was high. Simulated responses to the 1986 drought indicated that initial soil water potentials at planting affected survival at values of less than −0.064 MPa in a sandy soil. Simulated growth was very sensitive to the photosynthetic rate, less sensitive to initial soluble carbohydrate concentration, and insensitive to instantaneous carbon allocation in relation to drought stress. The predicted increase in total root length for 1985 corresponded to the responses reported in several controlled environmental studies, but these were generally higher than those reported under field conditions. The results suggest that the carbon balance algorithm represents potential root growth within the constraints imposed by the model assumptions. The extreme diurnal fluctuations in plant water potential indicate that one or more important components of the plant system used to regulate short-term drought stress are not represented. Both stem tissue capacitance and the hydraulic conductance of mycorrhizal mycelia at low soil moisture contents may be important in controlling short-term water deficits. Further advances in the application of similar models depend upon an evaluation of these variables and a better theoretical and experimental determination of the effects of the geometry of the transplanted root system.

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