scholarly journals Use of stomatal resistance, photopigments, nitrogen, water potential, and radiation to estimate net photosynthesis in Liriodendron tulipifera L. A physiological index.

1973 ◽  
Author(s):  
C. J. Richardson ◽  
B. E. Dinger ◽  
W. F. Harris
Keyword(s):  
Water Potential ◽  
Net Photosynthesis ◽  
Liriodendron Tulipifera ◽  
Stomatal Resistance ◽  
Physiological Index

Effect of Water Deficit on Carbon Dioxide Exchange and Leaf Elongation Rate of Panicum maximum Var. trichoglume

1976 ◽  
Vol 3 (3) ◽  
pp. 401 ◽  
Author(s):  
MM Ludlow ◽  
TT Ng
Keyword(s):  
Carbon Dioxide ◽  
Water Potential ◽  
Leaf Water Potential ◽  
Net Photosynthesis ◽  
Stomatal Resistance ◽  
Leaf Water ◽  
Carbon Dioxide Exchange ◽  
Leaf Elongation ◽  
Water Deficits ◽  
Water Potentials

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.

Photosynthesis and Carbon Dioxide Transfer Resistance of Lodgepole Pine Seedlings in Relation to Irradiance, Temperature, and Water Potential

1974 ◽  
Vol 4 (2) ◽  
pp. 201-206 ◽  
Author(s):  
Gary F. Dykstra
Keyword(s):  
Carbon Dioxide ◽  
Water Potential ◽  
Environmental Conditions ◽  
Net Photosynthesis ◽  
Stomatal Resistance ◽  
Transfer Resistance ◽  
Pine Seedlings ◽  
Rate Limiting ◽  
Potential Maximum ◽  
Mesophyll Resistance

Photosynthesis and stomatal and total equivalent mesophyll resistances to CO2 transfer were measured in relation to irradiance, needle temperature, and tree water potential. Maximum rates of net photosynthesis were attained at 380 W m−2 irradiance, 20 °C needle temperature, and the highest tree water potential obtained, ca. −2.5 bars. Stomatal and total mesophyll resistances have a significant rate-limiting role when environmental conditions are less than optimum. Mesophyll resistance was larger than stomatal resistance under all environmental conditions.

Recovery After Water Stress of Leaf Gas Exchange in Panicum maximum var. trichoglume

1980 ◽  
Vol 7 (3) ◽  
pp. 299 ◽  
Author(s):  
MM Ludlow ◽  
TT Ng ◽  
CW Ford
Keyword(s):  
Abscisic Acid ◽  
Water Stress ◽  
Water Potential ◽  
Net Photosynthetic Rate ◽  
Net Photosynthesis ◽  
Recovery Phase ◽  
Stomatal Resistance ◽  
Leaf Water ◽  
Rate Of Recovery ◽  
The Relationship

Net photosynthesis of the last fully expanded leaf of P. maximum var. trichoglume was able to recover from leaf water potentials as low as -92 bar. The degree of stress experienced during the single drying cycle did not influence the maximum net photosynthetic rate attained during recovery, but the time taken to reach the maximum increased with the degree of stress experienced. During the first 24 h, the rate of recovery of net photosynthesis was mainly determined by the rate at which the water status improved. Leaves which experienced water potentials less than c. -40 bar had a slower rate of recovery of water potential than less stressed leaves. This was partially offset by higher rates of net photosynthesis. Furthermore, the relationship between leaf water potential and net photosynthesis recorded during the drying cycle was different from those measured during recovery. Thus different relationships must be used in models simulating behaviour during water stress and subsequent recovery. Stomatal resistance exerted greater control than intracellular resistance over net photosynthesis in the recovery phase, irrespective of the water potential before rewatering or whether plants were preconditioned to stress. Although abscisic acid concentration was positively related to leaf water potential and stomatal resistance during the drying cycle, the relationship between abscisic acid concentration and stomatal resistance during recovery was poor or absent. Sucrose and amino-acid nitrogen accumulated during stress and decreased during recovery. However, the level of non- structural carbohydrates or nitrogen compounds in the recovery phase did not appear to influence net photosynthetic rate or its components. In fact, the reverse appeared to occur: the rate of photosynthesis and growth seemed to determine the levels of these compounds.

Photosynthesis and Transpiration in Damaged and Undamaged Spruce Trees

1996 ◽  
Vol 51 (3-4) ◽  
pp. 200-210 ◽  
Author(s):  
Aloysius Wild ◽  
Peter Sabel ◽  
Lucia Wild-Peters ◽  
Ursula Schmieden
Keyword(s):  
Gas Exchange ◽  
Water Potential ◽  
Natural Habitat ◽  
Late Summer ◽  
Net Photosynthesis ◽  
Diurnal Course ◽  
Physiological Homeostasis ◽  
Use Efficiency ◽  
Needle Loss ◽  
Light Saturation Curves

Abstract The investigations presented here focus on the CO2/H2O gas exchange in damaged and undamaged spruce trees while using open-air measurements as well as measurements under defined conditions in the laboratory. The studies were performed at two different sites in the Hunsrück and the Westerwald mountains. In the laboratory the CO2/H2O gas exchange was measured on detached branches under controlled conditions in the course of two years. CO2 saturation curves were also generated. In addition CO2 compensation points were deter­ mined employing a closed system. In the natural habitat diurnal course measurements of photosynthesis and transpiration as well as light-saturation curves for photosynthesis were performed. In parallel with the photosynthesis and transpiration measurements, measurements of the water potential were taken at both locations. The photosynthetic capacity and transpiration rate show a typical annual course with pronounced maxima in spring and late summer and minima in summer and winter. The needles of the damaged trees exhibit higher transpiration rates and a distinct reduction in photosyn­ thesis than the needles of the undamaged trees during two seasons. The diurnal course measurements of net photosynthesis and transpiration show a maximum in photosynthesis and transpiration in the afternoon in May and September, but a characteristic midday depression in July. Photosynthesis was markedly lower and transpiration higher in the needles of the damaged trees. The damaged trees show a lower increase in the light and CO2 saturation curves and higher CO2 compensation points as compared to the undamaged trees. The water potential reaches much lower values during the course of the day in needles of the dam­ aged trees. The reduction of the photosynthetic rate on one hand and the increase in transpiration on the other hand result in an extreme lowering of the water use efficiency in photosynthesis. The damage to the thylakoid membranes and to the guard cells obviously results in a pro­ found disturbance of the physiological homeostasis of the needles and could thus lead to premature needle loss.

Daily and seasonal changes of water potential in cereals

1976 ◽  
Vol 273 (927) ◽  
pp. 565-580 ◽  
Keyword(s):  
Environmental Factors ◽  
Water Potential ◽  
Leaf Water Potential ◽  
Stomatal Closure ◽  
Leaf Age ◽  
Stomatal Resistance ◽  
Leaf Water ◽  
Wheat Crop ◽  
Growing Seasons ◽  
Winter Wheat Crop

The paper reports measurements of the water relations of a barley crop (cv. Proctor) and a winter wheat crop (cv. Maris Huntsman), grown on the same site at Sutton Bonington. Throughout the two growing seasons, days were chosen when hourly measurements could be made of leaf water potential, by means of a pressure chamber, and of stomatal resistance, by means of a diffusion porometer. Environmental factors, e.g. radiation, temperature, humidity, were recorded concurrently. Relationships between leaf water potential, stomatal resistance and environmental factors are explored and compared for the two cereals. In particular, as frequent measurements were made over two months, the influence of leaf age on responses to environmental factors can be examined. On selected days with bright sunshine and dry soil the response of both cereals to water stress is analysed with particular reference to the control of evaporation by stomatal closure

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