Effects of short-term NaCl stress on water relations and gas exchange of two jute species

Thirty-day-old seedlings of two jute species (Corchorus capsularis L. cv. JRC 212 and C. olitorius L. cv. JRO 632) were subjected to short-term salinity stress (160 and 200 mM NaCl for 1 and 2 d). Relative water content, leaf water potential, water uptake, transpiration rate, water retention, stomatal conductance, net photosynthetic rate and water use efficiency of both jute species decreased due to salinity stress. The decrease was greater in C. olitorius than in C. capsularis and with higher magnitude of stress. Greater accumulation of Na+ and Cl- and a lower ratio of K+/Na+ in the root and shoot of C. olitorius compared with C. capsularis were also recorded. Pretreatment of seedlings with kinetin (0.09 mM), glutamic acid (4 mM) and calcium nitrate (5 mM) for 24 h significantly improved net photosynthesis, transpiration and water use efficiency of salinity stressed plants, the effect being more marked in C. olitorius. Among the pre-treatment chemicals, calcium nitrate was most effective. This revised version was published online in August 2006 with corrections to the Cover Date.     

Photosynthetic characteristics in Brassica carinata hybrids and their parents as influenced by moisture stress

The response of Brassica carinata hybrids and their parents to moisture stress at different growth stages was studied. B. carinata 226 was found to be susceptible to stress at pre-flowering and post-flowering stages while B. carinata 241 at flowering stage. Neither the changes in stomatal conductance nor in chlorophyll content could fully explain the reduction in net photosynthetic rate (P_N) induced by stress. B. carinata 241 had higher leaf water potential (ψ_w) although, it had lower P_N compared to B. carinata 226. Both the parents had lower P_N as well as leaf ψ_w. The stress response of PN in hybrids followed that in their respective female parents. This revised version was published online in July 2006 with corrections to the Cover Date.     

Gas exchange inHardwickia binata after water stress and rewatering

The net photosynthetic rate (P_N), stomatal conductance (g_s) and transpiration (E) ofHardwickia binata Roxb. leaves were reduced due to decrease in the leaf water potential (ψ_w) from -2.0 to - 5.7 MPa. P_N partially recovered in the treated plants upon rewatering. Decrease in g_s due to water stress may be the main factor for reduction of P_N. This work was supported by a financial grant from the MNES, India to KP.     

Biomass Partitioning and Gas Exchange in Dalbergia sissoo seedlings under water stress

Biomass, leaf water potential (_l), net photosynthetic rate (P _N), transpiration rate (E), stomatal conductance (g _s), leaf to air temperature difference (T _diff), and instantaneous water use efficiency (WUE) were measured in the seedlings of Dalbergia sissoo Roxb. grown under irrigation of 20 (W₁), 14 (W₂), 10 (W₃), and 8 (W₄) mm. Treatments were maintained by re-irrigation when water content of the soil reached 7.4% in W₁, 5.6% in W₂, 4.3% in W₃, and 3.2% in W₄. Seedlings in a control (W₅) were left without irrigation after maintaining the soil field capacity (10.7%). Seedlings of W₁ had highest biomass that was one tenth in W₅. Biomass allocation was highest in leaf in W₂ and in root in W₄ and W₅ treatments. Difference between predawn leaf water potential (_Pd) and midday (_mid) increased with soil water stress and with vapour pressure deficit (VPD) in April and May slowing down the recovery in plant leaf water status after transpiration loss. P _N, E, and g _s declined and T _diff increased from W₁ to W₅. Their values were highly significant in April and May for the severely stressed seedlings of W₄ and W₅. P _N increased from 08:00 to 10:00 and E increased until 13:00 within the day for most of the seedlings whereas g _s decreased throughout the day from 08:00 to 17:00. P _N and E were highest in March but their values were low in January, February, April, and May. Large variations in physiological variables to air temperature, photosynthetically active radiation, and vapour pressure deficit (VPD) indicated greater sensitivity of the species to environmental factors. WUE increased from W₁ to W₂ but decreased drastically at high water stress particularly during hot summer showing a kind of adaptation in D. sissoo to water stress. However, low biomass and reduced physiological functions at <50% of soil field capacity suggest that this species does not produce significant biomass at severe soil water stress or drought of a prolonged period.     

Photosynthesis,transpiration, and water use efficiency of <Emphasis Type="Italic">Leymus dasystachys</Emphasis> on the Hunshandake desert

Net photosynthetic rate (P _N), transpiration rate (E), and stomatal conductance (g _s) declined from upper leaves to the lower ones during dry and rainy seasons, indicating that long-term carbon budget should take into account P _N variations for different leaf types. Relatively greater P _N in the dry season suggested that this species is more able to maintain higher P _N under drought, but the relatively higher E in the dry season might reduce water use efficiency (P _N/E) for the species. Significant correlations between P _N and g _s indicated that g _s may be the critical factor for P _N variability in the desert region.     

Integration of hydraulic and chemical signalling in the control of stomatal conductance and water status of droughted plants

We describe here an integration of hydraulic and chemical signals which control stomatal conductance of plants in drying soil, and suggest that such a system is more likely than control based on chemical signals or water relations alone. The determination of xylem [ABA] and the stomatal response to xylem [ABA] are likely to involve the water flux through the plant. (1) If, as seems likely, the production of a chemical message depends on the root water status (Ψ_r), it will not depend solely on the soil water potential (Ψ_s) but also on the flux of water through the soil-plant-atmosphere continuum, to which are linked the difference between Ψ_r and Ψ_s. (2) The water flux will also dilute the concentration of the message in the xylem sap. (3) The stomatal sensitivity to the message is increased as leaf water potential falls. Stomatal conductance, which controls the water flux, therefore would be controlled by a water-flux-dependent message, with a water-flux-dependent sensitivity. In such a system, we have to consider a common regulation for stomatal conductance, leaf and root water potentials, water flux and concentration of ABA in the xylem. In order to test this possibility, we have combined equations which describe the generation and effects of chemical signals and classical equations of water flux. When the simulation was run for a variety of conditions, the solution suggested that such common regulation can operate. Simulations suggest that, as well as providing control of stomatal conductance, integration of chemical and hydraulic signalling may also provide a control of leaf water potential and of xylem [ABA], features which are apparent from our experimental data. We conclude that the root message would provide the plant with a means to sense the conditions of water extraction (soil water status and resisance to water flux) on a daily timescale, while the short-term plant response to this message would depend on the evaporative demand.     

Water relations and photosynthesis in Cucumis sativus L. leaves under salt stress

Hydroponically grown cucumber plants were exposed to 14-d period of salinity (0, 50, 100 mM NaCl). NaCl caused reduction in the relative water content in the leaves. The Na⁺ content increased and the K⁺ content decreased. The net photosynthetic rate, stomatal conductance and transpiration rate were markedly decreased by all of the salt treatments. Salinity decreased also the maximum quantum efficiency of photosystem 2 (PS 2) determined as the variable to maximum fluorescence ratio, the photochemical quantum yield of PS 2 and the photochemical fluorescence quenching, while the non-photochemical quenching increased. Above results indicate that NaCl affects photosynthesis through both stomata closure and non-stomatal factors.     

Photosynthesis of six barley genotypes as affected by water stress

The effect of water stress on plant water status and net photosynthetic gas exchange (PN) in six barley genotypes (Hordeum vulgare L.) differing in productivity and drought tolerance was studied in a controlled growth chamber. Osmotic adjustment (OA), PN, stomatal conductance (gs), and the ratio intercellular/ambient. CO2 concentration (Ci/Ca) were evaluated at four different levels of soil water availability, corresponding to 75, 35, 25 and 15 % of total available water. Variability in OA capacity was observed between genotypes: the drought tolerant genotypes Albacete and Alpha showed higher OA than drought susceptible genotypes Express and Mogador. The genotype Albacete exhibited also higher PN than the others at low water potential (Ψ). The ratios of PN/gs and Ci/Ca showed that differences in photosynthetic inhibition between genotypes at low Ψ were probably due to nonstomatal effects. In Tichedrett, a landrace genotype with a very extensive root development, OA was not observed, however, it exhibited a capacity to maintain its photosynthetic activity under water stress. This revised version was published online in June 2006 with corrections to the Cover Date.     

云锦杜鹃夏季气体交换和水分利用效率日变化

云锦杜鹃净光合速率和气孔导度日变化曲线为"双峰"型,光合效率午间明显降低,主要由非气孔限制引起。表观量子效率和实际光化学效率的降低是非气孔限制形成和发展的深层原因。蒸腾速率的日变化为"单峰型",午间最高。水分利用效率早晚较高、午间较低。净光合速率、蒸腾速率、气孔导度和水分利用效率分别与一些环境因子的相关性达到0.01或0.05显著水平。利用多元逐步回归方法分别得到了净光合速率、胞间CO2浓度、蒸腾速率、气孔导度和水分利用效率与环境因子的最优方程。     

A coupled model of stomatal conductance, photosynthesis and transpiration

A model that couples stomatal conductance, photosynthesis, leaf energy balance and transport of water through the soil–plant–atmosphere continuum is presented. Stomatal conductance in the model depends on light, temperature and intercellular CO₂ concentration via photosynthesis and on leaf water potential, which in turn is a function of soil water potential, the rate of water flow through the soil and plant, and on xylem hydraulic resistance. Water transport from soil to roots is simulated through solution of Richards’ equation. The model captures the observed hysteresis in diurnal variations in stomatal conductance, assimilation rate and transpiration for plant canopies. Hysteresis arises because atmospheric demand for water from the leaves typically peaks in mid‐afternoon and because of uneven distribution of soil matric potentials with distance from the roots. Potentials at the root surfaces are lower than in the bulk soil, and once soil water supply starts to limit transpiration, root potentials are substantially less negative in the morning than in the afternoon. This leads to higher stomatal conductances, CO₂ assimilation and transpiration in the morning compared to later in the day. Stomatal conductance is sensitive to soil and plant hydraulic properties and to root length density only after approximately 10 d of soil drying, when supply of water by the soil to the roots becomes limiting. High atmospheric demand causes transpiration rates, LE, to decline at a slightly higher soil water content, θ_s, than at low atmospheric demand, but all curves of LE versus θ_s fall on the same line when soil water supply limits transpiration. Stomatal conductance cannot be modelled in isolation, but must be fully coupled with models of photosynthesis/respiration and the transport of water from soil, through roots, stems and leaves to the atmosphere.     

Water movement through Quercus rubra I. Leaf water potential and conductance during polycyclic growth

Two experiments examined simultaneous changes in leaf area (A_L), root length (L_r), stomatal conductance (g_s), leaf water potential (Ψ_L), transpiration and hydraulic plant conductance per unit leaf area (G) during the first three shoot cycles of northern red oak (Quercus rubra L.) grown under favourable and controlled conditions. Each shoot cycle consisted of bud swell, stem elongation, leaf expansion and rest; roots grew almost continuously. The g_s of all leaves decreased substantially while leaves of the newest flush were expanding and increased modestly when seedling leaf area remained constant. Overall, g_s decreased. The Ψ_L of mature leaves decreased during leaf expansion and increased by an equivalent amount during intervening periods. Possible explanations for the paired changes in g_s and Ψ_L are considered. Changes in G closely paralleled those of canopy g_s. These parallel changes during polycyclic seedling growth should act to keep seedling Ψ_L relatively constant as plant size increases and thereby help prevent Ψ_L from dropping to levels that would cause runaway embolism.     

Stomatal limitation of photosynthesis as affected by water stress and CO2 concentration

A water stress effect on photosynthesis and transpiration of wheat seedlings at 50-500 µmol(CO2) mol-1 was measured in an open gas exchange system. The limitation of photosynthesis by stomatal conductance was quantified by a stomatal control coefficient of the net photosynthetic rate. The stomatal control coefficient increased linearly as the water potential of root media decreased to -1 MPa, and it decreased with increasing CO2 concentration.     

Influence of salinity on Na+ and K+ accumulation, and gas exchange in Avicennia germinans

We analysed plant growth, ion accumulation, leaf water relations, and gas exchange of Avicennia germinans (L.) L. subjected to a long-term, controlled salinity gradient from 0 to 55 ‰. Growth and leaf area were affected by salinity higher than 10 ‰. As salinity increased, the predawn leaf water potential (Ψ_w) and leaf osmotic potential (Ψ_s) decreased. Leaf Ψ_w was at least −0.32 MPa lower than the Ψ_w of solution. Na⁺ and K⁺ ions explained about 78 % of decrease in Ψ_s. K⁺ tissue water concentration decreased by more than 60 % in all salinity treatments as compared with those grown at 0 ‰. Inversely, Na⁺ concentration in tissue water increased with nutrient solution salinity. The maximum net photosynthetic rate (P _N) and stomatal conductance (g _s) decreased by 68 and 82 %, respectively, as salinity increased from 0 to 55 ‰; the intercellular CO₂ concentration (C _i) followed the same trend. The P _N as a function of C _i showed that both the initial linear slope and upper plateau of the P _N vs. C _i curve were markedly affected by high salinity (40 and 55 ‰).     

Nonstomatal inhibition of photosynthesis by water stress. Reduction in photosynthesis at high transpiration rate without stomatal closure in field-grown tomato

Large underestimates of the limitation to photosynthesis imposed by stomata can occur because of an error in the standard method of calculating average substomatal pressures of carbon dioxide when heterogeneity of those pressures occurs across a leaf surface. Most gas exchange data supposedly indicating nonstomatal inhibition of photosynthesis by water stress could have this error. However, if no stomatal closure occurs, any reduction in photosynthesis must be due to nonstomatal inhibition of photosynthesis. Net carbon dioxide exchange rates and conductances to water vapor were measured under field conditions in upper canopy leaves of tomato plants during two summers in Beltsville, Maryland, USA. Comparisons were made near midday at high irradiance between leaflets in air with the ambient water vapor content and in air with a higher water content. The higher water content, which lowered the leaf to air water vapor pressure difference (VPD), was imposed either one half hour or several hours before measurements of gas exchange. In both seasons, and irrespective of the timing of the imposition of different VPDs, net photosynthesis increased 60% after decreasing the VPD from 3 to 1 kPa. There were no differences in leaf conductance between leaves at different VPDs, thus transpiration rates were threefold higher at 3 than at 1 kPa VPD. It is concluded that nonstomatal inhibition of photosynthesis did occur in these leaves at high transpiration rate.     

Leaf gas exchange of cassava as affected by quality of planting material and water stress

Field trial was conducted to study the effects of quality of planting material and prolonged water stress on leaf gas exchange of the cassava (Manihot esculenta Crantz) cultivar M Col 1684. Nutrient contents of planting material affected rootlet formation, but not leaf gas exchange. Net photosynthetic rate (PN), stomatal conductance (gs), and intercellular CO2 concentration (Ci) were significantly reduced by prolonged water stress. New leaves developed after recovery from water stress showed higher PN and gs, as compared to leaves of similar ages of unstressed plants. The higher PN was associated with higher leaf nutrient contents, indicating that photosynthetic capacity was enhanced in these leaves. These compensating characteristics may partly explain the small yield reduction often observed in stressed cassava.     

Influence of water stress on leaf photosynthetic characteristics in wheat cultivars differing in their susceptibility to drought

A gradual reduction in leaf water potential (Ψ_leaf), net photosynthetic rate (P _N), stomatal conductance, and transpiration rate was observed in two drought tolerant (C 306 and K 8027) and two susceptible (RW 893 and 899) genotypes subjected to water stress. The extent of reduction was lower in K 8027 and C 306 and higher in RW 893 and RW 899. Rewatering the plants after 5 d of stress restored P _N and other gas exchange traits in all four cultivars. Water stress had no significant effect on variable to maximum fluorescence ratio (F_v/F_m) indicating that water stress had no effect on primary photochemistry of photosystem 2 (PS2). However, water stress reduced the efficiency of excitation energy transfer (F′_v/F′_m) and the quantum yield of electron transport (Φ_PS2). The reduction was more pronounced in susceptible cultivars. Water stress had no significant effect on photochemical quenching, however, the non-photochemical quenching increased by water stress.     

Response of cassava (Manihot esculenta Crantz) to water stress and fertilization

Experiments done in Santander de Quilichao (Cauca, Colombia) on two cassava cultivars indicated that cassava had at least three defence mechanisms against water deficit, enabling it to assimilate and store photosynthates in roots, even during prolonged droughts. These mechanisms include partial stomatal closure, ability of leaves to maintain reasonable net photosynthetic rate for long periods of water stress, reduced leaf area, and exploration of water from deep soil layers. While cassava responded positively to fertilization, no significant statistical differences were found between treatments of stress and non-stress, confirming cassava's ability to tolerate soil water deficit. This revised version was published online in June 2006 with corrections to the Cover Date.     

Xylem cavitation and hydraulic control of stomatal conductance in Laurel (Laurus nobilis L.)

The possible link between stomatal conductance (g_L), leaf water potential ( Ψ _L) and xylem cavitation was studied in leaves and shoots of detached branches as well as of whole plants of Laurus nobilis L. (Laurel). Shoot cavitation induced complete stomatal closure in air‐dehydrated detached branches in less than 10 min. By contrast, a fine regulation of g_L in whole plants was the consequence of Ψ _L reaching the cavitation threshold ( Ψ _CAV) for shoots. A pulse of xylem cavitation in the shoots was paralleled by a decrease in g_L of about 50%, while Ψ _L stabilized at values preventing further xylem cavitation. In these experiments, no root signals were likely to be sent to the leaves from the roots in response to soil dryness because branches were either detached or whole plants were growing in constantly wet soil. The stomatal response to increasing evaporative demand appeared therefore to be the result of hydraulic signals generated during shoot cavitation. A negative feedback link is proposed between g_L and Ψ _CAV rather than with Ψ _L itself.