Water Relations of Cotton. II. Continuous Estimates of Plant Water Potential from Stem Diameter Measurements 1

1977 ◽  
Vol 69 (4) ◽  
pp. 593-597 ◽  
Author(s):  
Morris G. Huck ◽  
Betty Klepper
2010 ◽  
Author(s):  
Vasu Udompetaikul ◽  
Shrini K Upadhyaya ◽  
David C Slaughter ◽  
Bruce D Lampinen

2011 ◽  
Vol 47 (1) ◽  
pp. 27-51 ◽  
Author(s):  
M. K. V. CARR

SUMMARYThe results of research on the water relations and irrigation needs of coconut are collated and summarized in an attempt to link fundamental studies on crop physiology to drought mitigation and irrigation practices. Background information on the centres of origin and production of coconut and on crop development processes is followed by reviews of plant water relations, crop water use and water productivity, including drought mitigation. The majority of the recent research published in the international literature has been conducted in Brazil, Kerala (South India) and Sri Lanka, and by CIRAD (France) in association with local research organizations in a number of countries, including the Ivory Coast. The unique vegetative structure of the palm (stem and leaves) together with the long interval between flower initiation and the harvesting of the mature fruit (44 months) mean that causal links between environmental factors (especially water) are difficult to establish. The stomata play an important role in controlling water loss, whilst the leaf water potential is a sensitive indicator of plant water status. Both stomatal conductance and leaf water potential are negatively correlated with the saturation deficit of the air. Although roots extend to depths >2 m and laterally >3 m, the density of roots is greatest in the top 0–1.0 m soil, and laterally within 1.0–1.5 m of the trunk. In general, dwarf cultivars are more susceptible to drought than tall ones. Methods of screening for drought tolerance based on physiological traits have been proposed. The best estimates of the actual water use (ETc) of mature palms indicate representative rates of about 3 mm d−1. Reported values for the crop coefficient (Kc) are variable but suggest that 0.7 is a reasonable estimate. Although the sensitivity of coconut to drought is well recognized, there is a limited amount of reliable data on actual yield responses to irrigation although annual yield increases (50%) of 20–40 nuts palm−1 (4–12 kg copra, cultivar dependent) have been reported. These are only realized in the third and subsequent years after the introduction of irrigation applied at a rate equivalent to about 2 mm d−1 (or 100 l palm−1 d−1) at intervals of up to one week. Irrigation increases female flower production and reduces premature nut fall. Basin irrigation, micro-sprinklers and drip irrigation are all suitable methods of applying water. Recommended methods of drought mitigation include the burial of husks in trenches adjacent to the plant, mulching and the application of common salt (chloride ions). An international approach to addressing the need for more information on water productivity is recommended.


1984 ◽  
Vol 102 (2) ◽  
pp. 415-425 ◽  
Author(s):  
M. McGowan ◽  
P. Blanch ◽  
P. J. Gregory ◽  
D. Haycock

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.


1975 ◽  
Vol 2 (4) ◽  
pp. 489 ◽  
Author(s):  
BR Tunstall ◽  
DJ Connor

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.


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