Drought acclimation of two deciduous tree species of different layers in a temperate forest canopy

Water-use strategies of Populus tremula and Tilia cordata, and the role of abscisic acid in these strategies, were analysed. P. tremula dominated in the overstorey and T. cordata in the lower layer of the tree canopy of the temperate deciduous forest canopy. Shoot water potential (), bulk-leaf abscisic acid concentration ([ABA]_leaf), abscisic acid concentration in xylem sap ([ABA]_xyl), and rate of stomatal closure following the supply of exogenous ABA (v) decreased acropetally through the whole tree canopy, and foliar water content per area (w), concentration of the leaf osmoticum (c), maximum leaf-specific hydraulic conductance of shoot (L), stomatal conductance (g_s), and the threshold dose per leaf area of the exogenous ABA (d_a) required to reduce stomatal conductance increased acropetally through the tree canopy (from the base of the foliage of T. cordata to the top of the foliage of P. tremula) in non-stressed trees. The threshold dose per leaf dry mass of the exogenous ABA (d_w) required to reduce stomatal conductance, was similar through the tree canopy. After a drought period (3 weeks), the , w, L, g_s, d_a and d_w had decreased, and c and v had increased in both species. Yet, the effect of the drought period was more pronounced on L, g_s, d_a, d_w and v in T. cordata, and on , w and c in P. tremula. It was concluded that the water use of the species of the lower canopy layer—T. cordata, is more conservative than that of the species of the overstorey, P. tremula. [ABA]_leaf had not been significantly changed in these trees, and [ABA]_xyl had increased during the drought period only in P. tremula. The relations between [ABA]_leaf, [ABA]_xyl and the stomatal conductance, the osmotic adjustment and the shoot hydraulic conductance are also discussed.     

Mechanisms contributing to seasonal homeostasis of minimum leaf water potential and predawn disequilibrium between soil and plant water potential in Neotropical savanna trees

Seasonal regulation of leaf water potential (_L) was studied in eight dominant woody savanna species growing in Brazilian savanna (Cerrado) sites that experience a 5-month dry season. Despite marked seasonal variation in precipitation and air saturation deficit (D), seasonal differences in midday minimum _L were small in all of the study species. Water use and water status were regulated by a combination of plant physiological and architectural traits. Despite a nearly 3-fold increase in mean D between the wet and dry season, a sharp decline in stomatal conductance with increasing D constrained seasonal variation in minimum _L by limiting transpiration per unit leaf area (E). The leaf surface area per unit of sapwood area (LA/SA), a plant architectural index of potential constraints on water supply in relation to transpirational demand, was about 1.5–8 times greater in the wet season compared to the dry season for most of the species. The changes in LA/SA from the wet to the dry season resulted from a reduction in total leaf surface area per plant, which maintained or increased total leaf-specific hydraulic conductance (G_t) during the dry season. The isohydric behavior of Cerrado tree species with respect to minimum _L throughout the year thus was the result of strong stomatal control of evaporative losses, a decrease in total leaf surface area per tree during the dry season, an increase in total leaf-specific hydraulic conductance, and a tight coordination between gas and liquid phase conductance. In contrast with the seasonal isohydric behavior of minimum _L, predawn _L in all species was substantially lower during the dry season compared to the wet season. During the dry season, predawn _L was more negative than bulk soil estimated by extrapolating plots of E versus _L to E=0. Predawn disequilibrium between plant and soil was attributable largely to nocturnal transpiration, which ranged from 15 to 22% of the daily total. High nocturnal water loss may also have prevented internal water storage compartments from being completely refilled at night before the onset of transpiration early in the day.     

Stomatal response to leaf water potential in almond trees under drip irrigated and non irrigated conditions

Almond plants (Amygdalus communis L. cv. Garrigues) were grown in the field under drip irrigated and non irrigated conditions. Leaf water potential () and leaf conductance (g₁) were determined at three different times of the growing season (spring, summer and autumn). The relationships between and g₁ in both treatments showed a continuous decrease of g₁ as decreased in spring and summer. Data from the autumn presented a threshold value of (approx. –2.7 MPa in dry treatment, and approx. –1.4 MPa in wet treatment) below which leaf conductance remained constant.     

Water relations of crok-oak (Quercus suber L.) under natural conditions

Daily and annual courses of leaf transpiration, stomatal conductance and shoot water potential of four Quercus suber individuals were compared in a semi-natural stand in southwest Portugal, from spring 1989 to early summer 1990.The trees investigated showed annual patterns typical of evergreen sclerophyllous species but varied in their range of stomatal operation. This appeared to be related to differences in hydraulic conductivity in the root-to-leaf pathway.Maximum stomatal conductance and transpiration rates occurred from March to June.Water stress was found to be moderate and winter cold stress due to low air and soil temperatures appeared to have an influence on plant water balance through their effects on flow resistances.Abbreviations g_sw stomatal conductance - g_max maximum stomatal conductance - PAR photosynthetically active radiation - RH relative humidity of the air - T leaf transpiration - Ta air temperature - TL leaf temperature - T_max maximum leaf transpiration - W air-to-leaf vapor pressure difference - shoot water potential - PD predawn shoot water potential - MIN minimum shoot water potential     

Xylem development and hydraulic conductance in sun and shade shoots of grapevine (Vitis vinifera L.): evidence that low light uncouples water transport capacity from leaf area

Morphology, water relations, and xylem anatomy of high-light (sun)- and low-light (shade)-grown Vitis vinifera L. shoots were studied to determine the effects of shading on the hydraulic conductance of the pathway for water flow from the roots to the leaves. Shade shoots developed leaf area ratios (leaf area: plant dry weight) that were nearly threefold greater than sun shoots. Water-potential gradients (·m^–1) in the shoot xylem accounted for most of the ·m^–1 between soil and shoot apex at low and high transpiration rates in both sun and shade shoots, but the gradients were two- to fourfold greater in shade-grown plants. Low light reduced xylem conduit number in petioles, but had an additional slight effect on conduit diameter in internodes. The hydraulic conductance per unit length (Kh) and the specific hydraulic conductivity (k_s, i.e. Kh per xylem cross-sectional area) of internodes, leaf petioles, and leaf laminae at different developmental stages leaf plastochron index was calculated from measurements of water potential and water flow in intact plants, from flow through excised organs, and from vessel and tracheid lumen diameters according to Hagen-Poiseuille's equation. For all methods and conductance parameters, the propensity to transport water to sink leaves was severalfold greater in internodes than in petioles. The Kh and k_s increased logarithmically until growth ceased, independent of treatment and measurement method, and increased further in pressurized-flow experiments and Hagen-Poiseuille predictions. However, the increase was less in shade internodes than in sun internodes. Mature internodes of shade-grown plants had a two- to fourfold reduced Kh and significantly lower k_s than sun internodes. Except very early in development, leaf lamina conductance and k_s from shade-grown plants was also reduced. The strong reduction in Kh with only a slight reduction in leaf area (17% of sun shoots) in the shade shoots indicated a decoupling of water-transport capacity from the transpirational surface supplied by that capacity. This decoupling resulted in strongly reduced leaf specific conductivities and Huber values for both internodes and petioles, which may increase the likelihood of cavitation under conditions of high evaporative demand or soil drought.Abbreviations A_c total cross-sectional area (internodes, petioles, leaf laminae) - A_x xylem cross-sectional area - HV Huber value - Kh hydraulic conductance per unit length - k_s specific hydraulic conductivity - LPI leaf plastochron index - LSC leaf specific conductivity - water potential - water-potential gradient - q volume flow of water per unit time Hans R. Schultz was supported in part by the Deutsche Forschungsgemeinschaft (grant Ki-114/8-1). We wish to thank Dr. Thomas Geier, Institut für Biologie, Forschungsanstalt D-6222 Geisenheim, Germany for his advice on sample preparation and microscopy, and two anonomous reviewers for their helpful comments.     

Drought resistance of 2-year-old saplings of Mediterranean forest trees in the field: relations between water relations,hydraulics and productivity

Drought resistance was examined for 2-year-old saplings of Ceratonia siliqua L., Olea oleaster Hoffmgg. et Link., Quercus suber L. and Q. pubescens Willd. growing in the field in Sicily, with the aim of testing their possible use in the reforestation of degraded areas. To this purpose, leaf conductance to water vapour (g _L), transpiration rate (E _L), relative water content (RWC) and water potential (_L) were measured between pre-dawn and sunset, monthly from May to November. Parallel measurements of loss of hydraulic conductance of twigs of the current year (PLC) were made together with an estimate of whole-plant hydraulic conductance (K _PLANT) on the basis of the ratio of maximum E _L to (_PD-_MIN), where _PD is pre-dawn _L and _MIN is the minimum diurnal _L. C. siliqua saplings maintained high g _L throughout the study period with high RWC (over 90%) and _L. They grew rapidly and increased their foliage area (A _L) by over 60% from May to winter rest. This was accompanied by low twig PLC (about 20% in September) resulting in high K _PLANT all through the study period. In contrast, O. oleaster saplings underwent distinct dehydration in July, i.e. they showed stomatal closure due to a drop in RWC (to 75%) and _L (to the turgor-loss point). This was apparently due to twig cavitation, resulting in a strong decrease of K _PLANT. Plants, however, tolerated summer drought, and showed growth (A _L increased by 15% from May to November). Saplings of Q. suber and Q. pubescens were much more vulnerable to twig cavitation (PLC was 35–48% from June to November) than the other two species, and their average K _PLANT was lower. Saplings of Q. suber and Q. pubescens grew only during the wet spring period, and no new foliage was produced thereafter. Changes in twig hydraulic conductance played a dominant role in determining changes in K _PLANT in that the two variables were well correlated to each other (r=0.68 for P=0.001). We conclude that C. siliqua is an ideal candidate for reforestation of Sicilian degraded areas as is O. oleaster that, however, requires some additional water supply in the summer, at least during the early years after plantation. In wetter locations of Sicily, to an altitude between 0 and 500 m, Q. suber and Q. pubescens can be used for reforestation with expected higher competitiveness of the latter over the former species.     

The effect of humidity and light on cellular water relations and diffusion conductance of leaves ofTradescantia virginiana L.

Turgor (_p) and osmotic potential (_s) in epidermal and mesophyll cells, in-situ xylem water potential (-xyl) and gas exchange were measured during changes of air humidity and light in leaves ofTradescantia virginiana L., Turgor of single cells was determined using the pressure probe. Sap of individual cells was collected with the probe for measuring the freezing-point depression in a nanoliter osmometer. Turgor pressure was by 0.2 to 0.4 MPa larger in mesophyll cells than in epidermal cells. A water-potential gradient, which was dependent on the rate of transpiration, was found between epidermis and mesophyll and between tip and base of the test leaf. Step changes of humidity or light resulted in changes of epidermal and mesophyll turgor (_p-epi, _p-mes) and could be correlated with the transpiration rate. Osmotic potential was not affected by a step change of humidity or light. For the humidity-step experiments, stomatal conductance (g) increased with increasing epidermal turgor.g/_p-epi appeared to be constant over a wide range of epidermal turgor pressures. In light-step experiments this type of response was not found and stomatal conductance could increase while epidermal turgor decreased.Symbols E transpiration - g leaf conductance - w leaf/air vapour concentration difference - -epi water potential of epidermal cells - -mes water potential of mesophyll cells - -xyl water potential of xylem - _p-epi turgor pressure of epidermal cells - _p-mes turgor pressure of mesophyll cells - _s-epi osmotic potential of epidermal cells - _s-mes osmotic potential of mesophyll cells     

Root and stem xylem embolism,stomatal conductance,and leaf turgor in Acer grandidentatum populations along a soil moisture gradient

The objective of this study was to determine how adjustment in stomatal conductance (g ^s) and turgor loss point (_tlp) between riparian (wet) and neighboring slope (dry) populations of Acer grandidentum Nutt. was associated with the susceptibility of root versus stem xylem to embolism. Over two summers of study (1993–1994), the slope site had substantially lower xylem pressures (_px) and g ^s than the riparian site, particularly during the drought year of 1994. The _tlp was also lower at the slope (-2.9±0.1 MPa; all errors 95% confidence limits) than at riparian sites (-1.9±0.2 MPa); but it did not drop in response to the 1994 drought. Stem xylem did not differ in vulnerability to embolism between sites. Although slope-site stems lost a greater percentage of hydraulic conductance to embolism than riparian stems during the 1994 drought (46±11% versus 27±3%), they still maintained a safety margin of at least 1.7 MPa between midday _px and the critical pressure triggering catastrophic xylem embolism (_pxCT). Root xylem was more susceptible to embolism than stem xylem, and there were significant differences between sites: riparian roots were completely cavitated at -1.75 MPa, compared with -2.75 MPa for slope roots. Vulnerability to embolism was related to pore sizes in intervessel pit membranes and bore no simple relationship to vessel diameter. Safety margins from _pxCT averaged less than 0.6 MPa in roots at both the riparian and slope sites. Minimal safety margins at the slope site during the drought of 1994 may have led to the almost complete closure of stomata (g _s=9±2 versus 79±15 mmol m^-2 s^-1 at riparian site) and made any further osmotic adjustment of _tlp non-adaptive. Embolism in roots was at least partially reversed after fall rains. Although catastrophic embolism in roots may limit the minimum for gas exchange, partial (and reversible) root embolism may be adaptive in limiting water use as soil water is exhausted.     

Gas Exchange,Photochemical Efficiency,and Leaf Water Potential in Three Salix Species

Gas exchange, photochemical efficiency, and leaf water potential (_l) of Salix matsudana (non-indigenous species), S. microstachya and S. gordejevii (indigenous species) were studied in Hunshandak Sandland, China. _l of all the three species decreased from 06:00 to 12:00, and increased afterwards. S. matsudana showed higher values of _l than others. Net photosynthetic rate (P _N) and stomatal conductance (g _s) of S. matsudana were the lowest among all, with the maximum P _N at 10:00 being 75% of that of S. gordejevii. Compared with the indigenous species, the non-indigenous S. matsudana had also lower transpiration rate (E) and water use efficiency (WUE). The values of F_v/F_m in all the species were lower from 06:00 to 14:00 than those after 14:00, indicating an obvious depression in photochemical efficiency of photosystem 2 in both non-indigenous and native species. However, it was much more depressed in S. matsudana, the non-indigenous tree. P _N was positively correlated to g _s and negatively related to _l. The relationship between g _s and vapour pressure difference (VPD) was exponential, while negative linear correlation was found between g _s and _l.     

Xylem cavitation in excised leaves of Malus sylvestris Mill. and measurement of leaf water status with the pressure chamber

Summary A change occurs in the relationship between xylem water potential (_x) measured with the pressure chamber and leaf water potential ((_w)) when a period of post-excision water loss is allowed before measurement of (_x) and (_x). When this occurs, water stress is over-estimated by the pressure chamber measurement. Over the same period of water loss, cavitation vibrations have been detected acoustically in excised leaves. It is suggested that the measurement of (_x) is affected by emptying of some of the xylem vessels due to cavitation. This would require that additional pressure be applied to a leaf in the pressure chamber in order to measure (_x).     

Effects of Osmotic Drought Stress Induced by a Combination of NaCl and Polyethylene Glycol on Leaf Water Status,Photosynthetic Gas Exchange,and Water Use Efficiency of Pistacia khinjuk and P. mutica

Leaf water potential, leaf osmotic potential, chlorophyll a and b contents, stomatal conductance, net photosynthetic rate, and water use efficiency were determined in two pistachio species (Pistacia khinjuk L. and P. mutica L.) grown under osmotic drought stress induced by a combination of NaCl and polyethylene glycol 6000. A decrease in values for all mentioned variables was observed as the osmotic potential of the nutrient solution (_s) decreased. The osmotic adjustment () of the species increased by decreasing _s. Thus P. khinjuk had a higher osmotic drought stress tolerance than P. mutica.     

Drought stress influences leaf water content,photosynthesis, and water-use efficiency of <Emphasis Type="Italic">Hibiscus rosa-sinensis</Emphasis> at three potassium concentrations

The influence of drought stress (DS) upon whole-plant water content, water relations, photosynthesis, and water-use efficiency of Hibiscus rosa-sinensis cv. Leprechaun (Hibiscus) plants at three levels of potassium (K) nutritional status were determined after a 21-d gradually imposed DS treatment. Compared to K-deficient plants, adequate K supply improved the leaf water content (LWC) and leaf water relations of Hibiscus by decreasing the , and generally sustained rates of net photosynthesis (P _N) and transpiration (E), and stomatal conductance (g _s), both in DS and non-DS plants. In K-deficient Hibiscus, LWC, turgor potential ( _P), and P _N, E, and g _s as well as instantaneous water-use efficiency, WUE (P _N/E) were consistently lower, compared to K-sufficient plants. Carbon isotope discrimination () was lower (i.e. longterm WUE was greatest) in DS than non-DS plants, but K had no effect on during the 21-d drought treatment period under glasshouse conditions. However, the trend in the value of DS plants suggests that could be a useful index of the response of Hibiscus to DS under glasshouse growing conditions. Thus the incorporation of a properly controlled fertilization regime involving sufficient levels of K can improve the acclimation of P _N to low _leaf, increase P _N/E of Hibiscus, and may have potential benefit for other woody plants species.     

Water relations and xylem transport of nutrients in pepper plants grown under two different salts stress regimes

Two iso-osmotic concentrations of NaCl and Na₂SO₄ were used for discriminating between the effects of specific ion toxicities of salt stress on pepper plants (Capsicum annuum L.) grown in hydroponic conditions, in a controlled-environment greenhouse. The two salts were applied to plants at different electrical conductivities, and leaf water relations, osmotic adjustment and root hydraulic conductance were measured. Leaf water potential (_w), leaf osmotic potential (_o) and leaf turgor potential (_p) decreased significantly when EC increased, but the decrease was less for NaCl- than for Na₂SO₄-treated plants. The reduction in stomatal conductance was higher for NaCl-treated plants. There were no differences in the effect of both treatments on the osmotic adjustment, and a reduction in root hydraulic conductance and the flux of solutes into the xylem was observed, except for the saline ions (Na⁺, Cl^– and SO₄ ^2–). Therefore, pepper growth decreased with increasing salinity because the plants were unable to adjust osmotically or because of the toxic effects of Cl^–, SO₄ ^2– and/or Na⁺. However, turgor of NaCl-treated plants was maintained at low EC (3 and 4 dS m^–1) probably due to the maintenance of water transport into the plant (decrease of stomatal conductance), which, together with the lower concentration of Na⁺ in the plant tissues compared with the Na₂SO₄ treatment, could be the cause of the smaller decrease in growth.     

CO2 Assimilation and Water Relations of Almond Tree (Prunus amygdalus Batsch) Cultivars Grown Under Field Conditions

Gas exchanges and leaf water potential (_w) of six-years-old trees of fourteen Prunus amygdalus cultivars, grafted on GF-677, were studied in May, when fruits were in active growing period, and in October, after harvesting. The trees were grown in the field under rain fed conditions. Predawn _w showed lower water availability in October compared with May. The lowest _w values at midday in May increased gradually afterwards, while in October they decreased progressively until night, suggesting a higher difficulty to compensate the water lost by transpiration. However, relative water content (RWC) measured in the morning was similar in both periods, most likely due to some rainfall that occurred in September and first days of October that could be enough to re-hydrate canopy without significantly increasing soil water availability. The highest net photosynthetic rate (P _N) was found in both periods early in the morning (08:00–11:00). Reductions in P _N from May to October occurred in most cultivars except in José Dias and Ferrastar. In all cultivars a decrease in stomatal conductance (g _s) was observed. Photosynthetic capacity (P _max) did not significantly change from spring to autumn in nine cultivars, revealing a high resistance of photosynthetic machinery of this species to environmental stresses, namely high temperature and drought. Osmotic adjustment was observed in some cultivars, which showed reductions of ca. 23 % (Duro d' Estrada, José Dias) and 15 % (Tuono) in leaf osmotic potential (). Such decreases were accompanied by soluble sugars accumulation. The Portuguese cultivar José Dias had a higher photosynthetic performance than the remaining genotypes.     

Gas Exchange and Chlorophyll Fluorescence Response to Simulated Rainfall in Hedysarum fruticosum var. mongolicum

The response of gas exchange and chlorophyll fluorescence along with changes in simulated rainfall were studied in water stressed plants Hedysarum fruticosum var. mongolicum (H.f.m.). Net photosynthetic rate (P _N), stomatal conductance (gs), leaf water potential (_leaf), and apparent carboxylation efficiency (P _N/C _i) were significantly increased with the increase of rainfall. However, they did not change synchronously. The complete recovery of both P _N and P _N/C _i appeared 3 d after watering while g _s and _leaf were recovered 1 d after treatment. Gas exchange characters increased sharply from 5 to 15 mm rainfall and then maintained steady state with increasing rainfall. During the initial phase of water recovery, photosystem 2 (PS2) activity was not affected and its complete recovery occurred also 3 d after rainfall. Hence the recovery of P _N was attributed to both opening of stomata and increase in carboxylation efficiency. Furthermore, PS2 activity was really impaired by water stress and could recover to the normal status when the water stress disappeared.     

Hydraulic conductance and water potential gradients in squash leaves showing mycorrhiza-induced increases in stomatal conductance

Stomatal conductance (g _s) and transpiration rates vary widely across plant species. Leaf hydraulic conductance (k _leaf) tends to change with g _s, to maintain hydraulic homeostasis and prevent wide and potentially harmful fluctuations in transpiration-induced water potential gradients across the leaf (ΔΨ _leaf). Because arbuscular mycorrhizal (AM) symbiosis often increases g _s in the plant host, we tested whether the symbiosis affects leaf hydraulic homeostasis. Specifically, we tested whether k _leaf changes with g _s to maintain ΔΨ _leaf or whether ΔΨ _leaf differs when g _s differs in AM and non-AM plants. Colonization of squash plants with Glomus intraradices resulted in increased g _s relative to non-AM controls, by an average of 27% under amply watered, unstressed conditions. Stomatal conductance was similar in AM and non-AM plants with exposure to NaCl stress. Across all AM and NaCl treatments, k _leaf did change in synchrony with g _s (positive correlation of g _s and k _leaf), corroborating leaf tendency toward hydraulic homeostasis under varying rates of transpirational water loss. However, k _leaf did not increase in AM plants to compensate for the higher g _s of unstressed AM plants relative to non-AM plants. Consequently, ΔΨ _leaf did tend to be higher in AM leaves. A trend toward slightly higher ΔΨ _leaf has been observed recently in more highly evolved plant taxa having higher productivity. Higher ΔΨ _leaf in leaves of mycorrhizal plants would therefore be consistent with the higher rates of gas exchange that often accompany mycorrhizal symbiosis and that are presumed to be necessary to supply the carbon needs of the fungal symbiont.     

Plant water relations and the effects of elevated CO2: a review and suggestions for future research

Increased ambient carbon dioxide (CO₂) has been found to ameliorate water stress in the majority of species studied. The results of many studies indicate that lower evaporative flux density is associated with high CO₂-induced stomatal closure. As a result of decreases in evaporative flux density and increases in net photosynthesis, also found to occur in high CO₂ environments, plants have often been shown to maintain higher water use efficiencies when grown at high CO₂ than when grown in normal, ambient air. Plants grown at high CO₂ have also been found to maintain higher total water potentials, to increase biomass production, have larger root-to-shoot ratios, and to be generally more drought resistant (through avoidance mechanisms) than those grown at ambient CO₂ levels. High CO₂-induced changes in plant structure (i.e., vessel or tracheid anatomy, leaf specific conductivity) may be associated with changes in vulnerability to xylem cavitation or in environmental conditions in which runaway embolism is likely to occur. Further study is needed to resolve these important issues. Methodology and other CO₂ effects on plant water relations are discussed.Abbreviations A net photosynthesis - C_a ambient [CO₂] - C_i internal [CO₂] - E evaporative flux density - g₁ leaf conductance - g_s stomatal conductance - LSC leaf specific conductivity - IRGA infrared gas analyzer - LAI leaf area index - PAR photosynthetically active radiation - total plant water potential - _soil soil water potential - _s solute potential - _pt turgor pressure potential - _px xylem pressure potential - RH relative humidity - R : S root to shoot ratio - RWC relative water content - SLA specific leaf area - SLW specific leaf weight - SPAC soil-plant-atmosphere-continuum - SWC soil water content - VPD vapor pressure deficit - WUE water use efficiency     

Stomatal conductance in a tropical xerophilous shrubland at a lava substratum

Diurnal variation in leaf stomatal conductance (g _s) of three xerophilous species (Buddleia cordata, Senecio praecox and Dodonaea viscosa) was measured over a 10-month period during the dry and wet seasons in a shrubland that is developing in a lava substratum in Mexico. Averaged stomatal conductances were 147 and 60.2 (B. cordata), 145 and 24.8 (D. viscosa) and 142.8 and 14.1 mmol m^–2 s^–1 (S. praecox) during the wet and dry season respectively. Leaf water potential () varied in a range of –0.6 to –1.2 (S. praecox), –0.6 to –1.8 (B. cordata) and –0.9 to –3.4 MPa (D. viscosa) during the same measurement periods. Stomata were more sensitive to changes in irradiance, air temperature and leaf–air vapour pressure difference in the rainy season than the dry season. Although stomatal responses to were difficult to distinguish in any season (dry or rainy), data for the entire period of measurement showed a positive correlation, stomata tending to open as increased, but there is strong evidence of isohydric behaviour in S. praecox and B. cordata. A multiplicative model relating g _s to environmental variables and to accounted for 79%–83% of the variation of g _s in three sites (pooled data); however, the performance of the model was poorer (60%–76%) for individual species from other sites not included in the pooled data.     

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.     

Control of light-induced bean leaf expansion: Role of osmotic potential,wall yield stress,and hydraulic conductivity

The role of three-turgor-related cellular parameters, the osmotic potential ( _s), the wall yield stress (Y) and the apparent hydraulic conductivity (L'p), in the initiation of ligh-induced expansion of bean (Phaseolus vulgaris L.) leaves has been determined. Although light causes an increase in the total solute content of leaf cells, the water uptake accompanying growth results in a slight increase in _s. Y is about 4 bar; and is unaffected by light. L'p, as calculated from growth rates and isopiestic measurements of leaf water potential, is only slightly greater in rapidly-growing leaves. The turgor pressure of growing cells is lower than that of the controls by about 35%. We conclude that light does not induce cell enlargement in the leaf by altering any of the above parameters, but does so primarily by increasing wall extensibility.Abbreviations and symbols RL red light - WL white light - L'p apparent hydraulic conductivity - OC osmotic concentration - Y wall yield stress - _s osmotic potential