Effects of Low Water Potentials on Transpiration and Photosynthesis in Mitchell Grass (Astrebla lappacea)

1974 ◽  
Vol 1 (4) ◽  
pp. 539 ◽  
Author(s):  
D Doley ◽  
NBA Trivett

Gas-exchange studies were carried out on potted Mitchell grass plants raised in the glasshouse and in growth cabinets. Provided that nutrition was adequate, the low irradiance of the growth cabinets did not impair the photosynthetic capacity at levels approaching full sunlight. The optimum temperature for net photosynthesis was in excess of 40�C. Close linear relationships were established between leaf water potential and both transpiration and net photosynthesis. Most of the variation in gas exchange could be attributed to changes in stomatal diffusive resistance. Although there was an increase in mesophyll resistance as leaf water potential decreased, the proportion of the total resistance attributable to the mesophyll became substantially smaller. Gas exchange exhibited a remarkable recovery after brief but severe drought, during which leaf water potentials fell to about -48 bars. There was some inhibition of both transpiration and photosynthesis for about one week following rewatering. It is concluded that A. lappacea demonstrates a high degree of true drought tolerance.

1976 ◽  
Vol 3 (3) ◽  
pp. 401 ◽  
Author(s):  
MM Ludlow ◽  
TT Ng

The responses of carbon dioxide exchange and leaf elongation of potted P. maximum var. trichoglume plants to water deficits were investigated in controlled environments and outdoors during drying cycles down to -92 bars leaf water potential, The sensitivities of net photosynthesis and leaf elongation to water deficits were similar. The leaf water potentials at which net photosynthesis and elongation ceased (c. -12 bars), and stomatal resistance increased substantially (- 6 bars), were relatively unaffected by nitrogen supply, environmental conditions during growth, and whether plants had previously experienced stress. However, these factors influenced the rate of net photosynthesis, at high leaf water potentials by affecting stomatal resistance and at moderate water potentials by affecting both stomatal and intracellular resistances. Stomata1 resistance was more sensitive than intracellular resistance to water deficits. Dark respiration rate decreased with leaf water potential, and was higher in plants receiving additional nitrogen. At moderate leaf water potentials (-7 to -9 bars), net photosynthesis of this C4 grass exhibited light saturation and rates similar to C3 plants. We suggest that the difference in behaviour of controlled-environment-grown and field-grown plants to water deficits observed with some species is unlikely to be due to differences in the aerial environment, but may result from differences in the rate at which stress develops. The ecological significance and evolution of the C4 syndrome are discussed briefly.


1974 ◽  
Vol 54 (4) ◽  
pp. 765-770 ◽  
Author(s):  
P. A. DUBÉ ◽  
K. R. STEVENSON ◽  
G. W. THURTELL

Relationships between (1) photosynthesis (2) transpiration (3) total diffusive resistance to water vapor and (4) mesophyll resistance and leaf water potential were examined in two lines of corn (Zea mays L.) differing in phenotypic response to water stress. One line (Q-188) was a wilting inbred and the other (DR-1) was an inbred known to have at least some heat and drought resistance under field conditions. No differences were found between inbred lines in net photosynthetic rate, transpiration rate and total diffusive resistance to water vapor at high or low leaf water potentials in the light. In both lines, stomatal closure began to occur between − 8.5 to − 9.5 bars. Similarly, rapid increases in both total resistance to water vapor diffusion and mesophyll resistance to carbon dioxide diffusion occurred within a narrow range of water potentials. However, leaf water potential, and thus all other parameters, differed markedly between lines when considered on a time scale. The early wilting of Q-188 suggested that high resistances to water flow were present in the xylem system.


Plants ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 311
Author(s):  
Vegas Riffle ◽  
Nathaniel Palmer ◽  
L. Federico Casassa ◽  
Jean Catherine Dodson Peterson

Unlike most crop industries, there is a strongly held belief within the wine industry that increased vine age correlates with quality. Considering this perception could be explained by vine physiological differences, the purpose of this study was to evaluate the effect of vine age on phenology and gas exchange parameters. An interplanted, dry farmed, Zinfandel vineyard block under consistent management practices in the Central Coast of California was evaluated over two consecutive growing seasons. Treatments included Young vines (5 to 12 years old), Control (representative proportion of young to old vines in the block), and Old vines (40 to 60 years old). Phenology, leaf water potential, and gas exchange parameters were tracked. Results indicated a difference in phenological progression after berry set between Young and Old vines. Young vines progressed more slowly during berry formation and more rapidly during berry ripening, resulting in Young vines being harvested before Old vines due to variation in the timing of sugar accumulation. No differences in leaf water potential were found. Young vines had higher mid-day stomatal conductance and tended to have higher mid-day photosynthetic rates. The results of this study suggest vine age is a factor in phenological timing and growing season length.


1994 ◽  
Vol 21 (3) ◽  
pp. 377 ◽  
Author(s):  
A Alvino ◽  
M Centritto ◽  
FD Lorenzi

Pepper (Capsicum annuum L.) plants were grown in 1 m2 lysimeters under two different water regimes in order to investigate differences in the spatial arrangements of the leaves and to relate this to daily assimilation rates of leaves of the canopy. The control regime (well-watered (W) treatment) was irrigated whenever the accumulated 'A' pan evaporation reached 4 cm, whereas the water-stressed (S) treatment was watered whenever the predawn leaf water potential fell below -1 MPa. During the growing cycle, equal numbers of sun and shade leaves were chosen from the apical, middle and basal parts of the canopy, corresponding to groups of leaves of increasing age. The CO2 exchange rate (CER) was measured at 0830, 1230 and 1530 hours on 8 days along the crop cycle, on leaves in their natural inclination and orientation. Leaf water potentials were measured on apical leaves before dawn and concurrently with gas exchange measurements. Control plants maintained predawn leaf water potential at -0.3 MPa, but S plants reached values lower than -1.2 MPa. Midday leaf water potentials were about twice as low in the S plants as in the controls. Water stress reduced LA1 during the period of crop growth, and dry matter production at harvest. Stressed apical leaves appeared to reduce stress by changing their inclination. They were paraheliotropic around midday and diaheliotropic at 0830 and 1530 hours. The CER values of the S treatment were significantly lower than those of the W treatment in apical and middle leaves, whereas the CER of basal leaves did not differ in either treatments. In the S treatment, reduction in the CER values of sunlit apical leaves was more evident in the afternoon than at midday or early in the morning, whereas basal leaves were less affected by water than basal stress leaves if sunlit, and negligibly in shaded conditions.


2007 ◽  
Vol 47 (12) ◽  
pp. 1484 ◽  
Author(s):  
B. Ben Rouina ◽  
A. Trigui ◽  
R. d'Andria ◽  
M. Boukhris ◽  
M. Chaïeb

In Tunisia, olives are grown under severe rain-fed, arid conditions. To determine the behaviour of olive trees (cv. Chemlali Sfax) during the severe drought affecting Tunisian arid areas in 2002, a range of physiological parameters were investigated in three adjacent orchards. Two olive orchards were rain-fed, one located on a sandy soil, and the other on a sandy-loam clay soil. A third orchard was also located on sandy soil, but received remedial irrigation (415 mm of water per year; ~40% of olive evapotranspiration). Predawn leaf water potential (Ψpd) did not fall below –1.52 MPa for irrigated olive trees. However, a large decrease in Ψpd was observed for rain-fed olive trees in the same period with Ψpd measured at about –3.2 MPa on sandy soil and –3.6 MPa on sandy-loam clay soil. At the same time, the minimal leaf water potential recorded at midday (Ψmin) decreased to –4.15 MPa and –4.71 MPa in the rain-fed trees for sandy and sandy-loam clay soil, respectively. For irrigated trees, the Ψmin was –1.95 MPa. These results were associated with relative water content, which varied from 80% for irrigated trees to 54 and 43.6%, respectively, for rain-fed trees and trees subjected to severe drought. In August, when the relative water content values were less than 50%, a progressive desiccation in the outer layer of canopy and death of terminal shoots were observed in trees, which grew on the sandy-loam clay soil. Furthermore, low soil water availability also affected (negatively) the net photosynthetic rate in rain-fed orchards (10.3 µmol/m2.s for irrigated trees v. 5.3 µmol/m2.s in rain-fed trees on sandy soil) and stomatal conductance (98.5 mmol/m2.s v. 69.3 mmol/m2.s). However, it improved water use efficiency (7.6 v. 4.7 µmol CO2/mmol H2O), which increased by more than 50% in both groups of rain-fed trees compared with the irrigated ones. We can conclude that olive trees respond to drought by showing significant changes in their physiological and biological mechanisms. These results also help our understanding of how olive trees cope with water stress in the field and how marginal soils can restrict growth and lower yields.


1976 ◽  
Vol 3 (2) ◽  
pp. 229 ◽  
Author(s):  
RD Graham

Leaf water potential, diffusive resistance, relative water content, weekly water use, yields and head bending were measured on wheat plants subjected to four copper levels (0, 0.4, 0.8 or 4.0 mg Cu per pot) and two water levels (6 or 12% soil water content). Severe copper deficiency (Cu 0) resulted in no grain yield, wilting, increased leaf diffusive resistance and, at the same time, increased leaf water potential relative to plants receiving 4.0 mg Cu (Cu 4.0). Water supply effects were observed but there was no interaction between copper and water treatments. Mild copper deficiency (Cu 0.4, Cu 0.8) resulted in small yield decreases, relative to Cu 4.0, and increased head bending towards maturity. It is concluded that wilting, characteristic of copper-deficient plants, is due to structural weakness (decreased lignification) and not to the water status of the plants; also, increased leaf diffusive resistance is due to a specific effect of copper deficiency on guard cells and not to decreased leaf water potential.


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