Measured and Calculated Transpiration in Trifolium repens under Different Water Potentials

The relationship between transpiration measured gravimetrically,a generalized transpiration equation, and the ratio VPD/r_leafwas investigated in Trifolium repens plants subjected to varyingwater potentials. Dawn leaf water potential was measured witha pressure chamber, leaf diffusion resistance with a diffusionporometer, leaf temperatures with a thermistor, and relativehumidity with an aspirated psychrometer. During drought transpirationrates determined by both methods were quite similar particularlyat the lowest water potentials. After rewatering calculatedrates were somewhat higher than measured ones. It is concludedthat transpiration calculated by the indirect method is a usefuland reasonable estimate of transpiration for single plants undervarying water potentials.     

The Relationship between Stem Diameter and Water Potentials in Stems of Young Cabbage Plants

Continuous measurements were made of stem shrinkage, stem waterpotential (₃) and transpiration rate (T) in young, pot-growncabbage plants subjected to cycling evaporative demands. Sequencesof increasing evaporative demands induced increases in T anddecreases in both ₃ and stem diameter and conversely, wheneverevaporative demand decreased, T declined and ₃ and stem diameterrose. Over short periods, stem water potentials and stem shrinkagewere virtually parallel even when rapid oscillations were induced.Over longer periods the effects of growth were important comparedwith those of water stress on stem diameter when the moisturecontent of the soil was high. Growth, however, ceased when theplant was subjected to relatively mild water stress (₃ = –0.4MPa). Stem diameters, after correction for growth, were linearlyrelated to plant water potential. The results suggest that stemshrinkage and only a few calibration measurements might be usedto provide continuous estimates of water potentials in fieldcrops. Key words: Cabbage, Stem diameter, Stem water potential     

Measurement of the Water Potential of Intact Plant Tissues1

A modified design of a thermocouple psychrometer is describedwhich utilizes the Peltier effect for producing an exceedinglysmall wet-bulb thermometer. The thermocouple assembly has beenreduced to miniature dimensions and the thermocouple chamberconsists of a silver cylinder (volume 0.06 cm³) whose base isformed by the material under observation. This makes it possibleto measure water potentials over limited surfaces of intactplant tissues, e.g. germinating pea seeds (Pisum sativum L.).The apparatus is capable of measuring water potentials downto a magnitude of about –6,000 joules/kg.³     

Rapid Oscillations in Plant Water Potential Measured with a Stem Psychrometer

Oscillations in water potential were measured for the firsttime in the plant stem. The phase of the oscillations in waterpotential (measured in Brussels sprout) lagged behind that oftranspiration by less than 5 min. The cycles ranged from 22to 48 min. The results support the view that oscillations inwater potential in the plant stem and interconnecting xylemtissues would synchronize oscillations in transpiration andstomatal opening throughout the plant. Brassica oleraceae L., Brussels sprout, oscillations, stem water potential, transpiration, stem psychrometer     

V-type H+-ATPase in the human eccrine sweat duct: immunolocalization and functional demonstration

We investigated for the presence of avacuolar-type H⁺-ATPase (V-ATPase) in the human eccrinesweat duct (SD). With the use of immunocytochemistry, ananti-V- ATPase antibody showed a strong staining at the apicalmembrane and a weaker one in the cytoplasm. Cold preservation followedby rewarming did not alter this staining pattern. With the use of thepH-sensitive dye2',7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein onisolated and perfused straight SD under HCO-free conditions and in the absence of Na⁺, proton extrusion wasdetermined from the recovery rate of intracellular pH(dpH_i/dt) following an acid load. Oligomycin (25 µM), an inhibitor of F-type ATPases, decreaseddpH_i/dt by 88 ± 6%, suggesting a role foran ATP-dependent process involved in pH_i recovery.Moreover, dpH_i/dt was inhibited at 95 ± 3% by 100 nM luminal concanamycin A, a specific inhibitor ofV-ATPases, whereas 10 µM bafilomycin A₁, another specificinhibitor of V-ATPases, was required to decrease dpH_i/dt by 73%. These results strongly suggestthat a V-ATPase is involved in proton secretion in the human eccrine SD.

     

Intracellular pH shifts in cultured kidney (A6) cells: effects on apical Na+ transport

We report, for the epithelialNa⁺ channel (ENaC) in A6 cells,the modulation by cell pH (pH_c)of the transepithelial Na⁺ current(I_Na), thecurrent through the individual Na⁺channel (i), the openNa⁺ channel density(N_o), and thekinetic parameters of the relationship betweenI_Na and theapical Na⁺ concentration. Thei andN_o were evaluatedfrom the Lorentzian I_Na noise inducedby the apical Na⁺ channel blocker6-chloro-3,5-diaminopyrazine-2-carboxamide.pH_c shifts were induced, understrict and volume-controlled experimental conditions, byapical/basolateral NH₄Cl pulses orbasolateral arrest of theNa⁺/H⁺exchanger (Na⁺ removal; block byethylisopropylamiloride) and were measured with the pH-sensitive probe2',7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein. Thechanges in pH_c were positivelycorrelated to changes inI_Na and theapically dominated transepithelial conductance. The sole pH_c-sensitive parameter underlyingI_Na wasN_o. Only thesaturation value of theI_Na kinetics wassubject to changes in pH_c.pH_c-dependent changes inN_o may be causedby influencingP_o, the ENaC openprobability, or/and the total channel number,N_T = N_o/P_o.

     

Effect of reactive oxygen species on NH4+ permeation in Xenopus laevis oocytes

To investigate theeffects of reactive oxygen species (ROS) on NHpermeation in Xenopus laevis oocytes, we used intracellulardouble-barreled microelectrodes to monitor the changes in membranepotential (V_m) and intracellular pH(pH_i) induced by a 20 mM NH₄Cl-containingsolution. Under control conditions, NH₄Cl exposure induceda large membrane depolarization (to V_m = 4.0 ± 1.5 mV; n = 21) and intracellularacidification [reaching a change in pH_i(pH_i) of 0.59 ± 0.06 pH units in 12 min]; theinitial rate of cell acidification (dpH_i/dt) was0.06 ± 0.01 pH units/min. Incubation of the oocytes in thepresence of H₂O₂ or -amyloid protein had nomarked effect on the NH₄Cl-induced pH_i. Bycontrast, in the presence of photoactivated rose bengal (RB),tert-butyl-hydroxyperoxide (t-BHP), orxanthine/xanthine oxidase (X/XO), the same experimental maneuverinduced significantly greater pH_i anddpH_i/dt. These increases in pH_iand dpH_i/dt were prevented by the ROS scavengershistidine and desferrioxamine, suggesting involvement of the reactivespecies ¹gO₂ and ·OH. Using thevoltage-clamp technique to identify the mechanism underlying theROS-measured effects, we found that RB induced a large increase in theoocyte membrane conductance (G_m). ThisRB-induced G_m increase was prevented by 1 mMdiphenylamine-2-carboxylate (DPC) and by a low Na⁺concentration in the bath. We conclude that RB, t-BHP, andX/XO enhance NH influx into the oocyte via activationof a DPC-sensitive nonselective cation conductance pathway.

     

Two-photon molecular excitation imaging of Ca2+ transients in Langendorff-perfused mouse hearts

The ability to image calciumsignals at subcellular levels within the intact depolarizing heartcould provide valuable information toward a more integratedunderstanding of cardiac function. Accordingly, a system combiningtwo-photon excitation with laser-scanning microscopy was developed tomonitor electrically evoked [Ca²⁺]_itransients in individual cardiomyocytes within noncontracting Langendorff-perfused mouse hearts. [Ca²⁺]_itransients were recorded at depths 100 µm from the epicardial surface with the fluorescent indicators rhod-2 or fura-2 in the presence of the excitation-contraction uncoupler cytochalasin D. Evoked[Ca²⁺]_i transients were highly synchronizedamong neighboring cardiomyocytes. At 1 Hz, the times from 90 to 50%(t_90-50%) and from 50 to 10%(t_50-10%) of the peak[Ca²⁺]_i were (means ± SE) 73 ± 4 and 126 ± 10 ms, respectively, and at 2 Hz, 62 ± 3 and94 ± 6 ms (n = 19, P < 0.05 vs.1 Hz) in rhod-2-loaded cardiomyocytes.[Ca²⁺]_i decay was markedly slower infura-2-loaded hearts (t_90-50% at 1 Hz,128 ± 9 ms and at 2 Hz, 88 ± 5 ms;t_50-10% at 1 Hz, 214 ± 18 ms and at2 Hz, 163 ± 7 ms; n = 19, P < 0.05 vs. rhod-2). Fura-2-induced deceleration of[Ca²⁺]_i decline resulted from increasedcytosolic Ca²⁺ buffering, because the kinetics of rhod-2decay resembled those obtained with fura-2 after incorporation of theCa²⁺ chelator BAPTA. Propagating calcium waves and[Ca²⁺]_i amplitude alternans were readilydetected in paced hearts. This approach should be of general utility tomonitor the consequences of genetic and/or functional heterogeneity incellular calcium signaling within whole mouse hearts at tissue depthsthat have been inaccessible to single-photon imaging.

     

Pacemaker potentials generated by interstitial cells of Cajal in the murine intestine

Pacemaker potentials were recorded in situ from myenteric interstitial cells of Cajal (ICC-MY) in the murine small intestine. The nature of the two components of pacemaker potentials (upstroke and plateau) were investigated and compared with slow waves recorded from circular muscle cells. Pacemaker potentials and slow waves were not blocked by nifedipine (3 µM). In the presence of nifedipine, mibefradil, a voltage-dependent Ca²⁺ channel blocker, reduced the amplitude, frequency, and rate of rise of upstroke depolarization (dV/dt_max) of pacemaker potentials and slow waves in a dose-dependent manner (1–30 µM). Mibefradil (30 µM) changed the pattern of pacemaker potentials from rapidly rising, high-frequency events to slowly depolarizing, low-frequency events with considerable membrane noise (unitary potentials) between pacemaker potentials. Caffeine (3 mM) abolished pacemaker potentials in the presence of mibefradil. Pinacidil (10 µM), an ATP-sensitive K⁺ channel opener, hyperpolarized ICC-MY and increased the amplitude and dV/dt_max without affecting frequency. Pinacidil hyperpolarized smooth muscle cells and attenuated the amplitude and dV/dt_max of slow waves without affecting frequency. The effects of pinacidil were blocked by glibenclamide (10 µM). These data suggest that slow waves are electrotonic potentials driven by pacemaker potentials. The upstroke component of pacemaker potentials is due to activation of dihydropyridine-resistant Ca²⁺ channels, and this depolarization entrains pacemaker activity to create the plateau potential. The plateau potential may be due to summation of unitary potentials generated by individual or small groups of pacemaker units in ICC-MY. Entrainment of unitary potentials appears to depend on Ca²⁺ entry during upstroke depolarization. pacemaker activity; slow waves; gastrointestinal motility; calcium channel     

Food and suspended sediment influences on the naupliar and copepodid durations of freshwater copepods: comparative studies on Tropodiaptomus and Metadiaptomus

Post-embryonic durations of Tropodiaptomus spectabilis (Kiefer)and Metadiaptomus colonialis(van Douwe) were determined at 20°Cin laboratory factorial experiments involving four algal foodenrichment levels (0, 100, 500 and 2500 µg l^–1 Cof Selenastrum added to 20 µm filtered water from respectivesource-lakes) and three suspended sediment levels (filtered,natural, and 2- to 3-fold sediment-enriched lake water). Foodeffects (30, 75, 225 and 600 (µg ^–1 C of Scenedesmus)were tested alone at 20°C for Metadiaptomus meridianus (vanDouwe). Total naupliar (D_n) and total copepodid (D_c) developmenttimes [summed to give total post-embryonic duration (D_t)] andmetasome lengths at maturity were measured In all taxa, foodsupply maximally affected D_c values 2- to 3-fold, whereas itsmaximal influence on D_n values was relatively slight (generally25%). The measured effect of food supply on D_t, was as strongas the predicted influence of temperature over an appropriateannual range. Food supply influenced size at maturity, and probablythereby fecundity, thus exerting additional demographic influences.Sediment effects were inconsistent, and quantitatively weakerthan food effects Total development of T.spectabilis was 20%raster, and that of M.colonialis 15% slower in sediment-enrichedthan in natural sediment level treatments; contrasting baselinesediment levels (2–3 times higher for the latter species)and different enrichment procedures confound interpretation.Unexpectedly, and inexplicably, development almost invariablyfailed in sediment-free water, implying an apparent dependencyon inorganic particles in these taxa This contrasts with thegenerally adverse influences of high sediment concentrationsupon zooplankton. Minimal male and female D_t values at 20°Cwere comparable and significantly longer in M.colonialis (15.5and 17 7 days) and M meridianus (16.5 and 21.5 days) than inT.spectabilis (11.7 and 12 2 days). These differences in durationare ecologically incongruous in relation to expected r –K life history strategies of genera characteristic of temporaryor semipermanent waters and permanent waters respectively.     

Is the Sense of Pi Levels Abolished in the pregc Strain of the Mold Neurospora crassa?

Comparison of some properties of alkaline phosphatase excretedby the mold Neurospora crassa and purified to apparent homogeneityby PAGE revealed that the preg^c strain excretes distinct molecularforms of this enzyme as a function of variations in extracellularP_i concentration, suggesting that this mutant strain is stillsensing P_i levels. (Received November 24, 1993; Accepted April 15, 1994)     

The Effects of Temperature, Soil-Water Potential, Irradiance, and their Interactions on CO2 Exchange Rates of two Sub-dominant Tropical Weeds

The effects of soil-water potential, temperature, and visibleirradiance interactions on net photo-synthetic and dark respirationrates of Pennisetum purpureum Schumach., a tropical C₄ grassand Calopogonium mucunoides Desv., a C₃ leguminous herb werestudied. The net photosynthetic rates of the two species decreased withdecreasing soil water potential and at all levels of irradianceconsidered. Similarly, the net photosynthetic rates of the twospecies decreased as soil water potential decreased at all temperatures. The C₄ species reached light saturation at very high irradiancewhereas the light saturation of the C₃ species occurred at relativelylow irradiance at high temperatures and low soil water potential. The dark respiration rates decreased with decreasing soil waterpotential and increased as temperature increased from 20 °Cto 40 °C. Key words: Soil water potential, Temperature, Irradiance, Photosynthesis, Respiration, Tropical weeds     

Theoretical and experimental errors for in situ measurements of plant water potential

Errors in psychrometrically determined values of leaf water potential caused by tissue resistance to water vapor exchange and by lack of thermal equilibrium were evaluated using commercial in situ psychrometers (Wescor Inc., Logan, UT) on leaves of Tradescantia virginiana (L.). Theoretical errors in the dewpoint method of operation for these sensors were demonstrated. After correction for these errors, in situ measurements of leaf water potential indicated substantial errors caused by tissue resistance to water vapor exchange (4 to 6% reduction in apparent water potential per second of cooling time used) resulting from humidity depletions in the psychrometer chamber during the Peltier condensation process. These errors were avoided by use of a modified procedure for dewpoint measurement. Large changes in apparent water potential were caused by leaf and psychrometer exposure to moderate levels of irradiance. These changes were correlated with relatively small shifts in psychrometer zero offsets (−0.6 to −1.0 megapascals per microvolt), indicating substantial errors caused by nonisothermal conditions between the leaf and the psychrometer. Explicit correction for these errors is not possible with the current psychrometer design.     

Aspects of the Water Relations of Ileostylus micranthus (Hook. f.) Tieghem, a New Zealand Mistletoe

Leaf water potentials in the mistletoe, Ileostylus micranthusgrowing outdoors decreased rapidly during the early part ofthe day but remained relatively steady in the early afternoondespite increases in atmospheric vapour pressure deficit (vpd).Minimum water potentials of the mistletoe were relatively constant.They were held at values lower than those of hosts when thelatter maintained high water potentials but approached or evenexceeded those of hosts when they developed low water potentials.In contrast, cut shoots of Ileostylus usually maintained higherwater contents and leaf water potentials than those of its hostswhen both were desiccated separately in the laboratory. Pressure-volumeanalyses indicated that Ileostylus had lower water potentialat full turgor, a lower water potential but higher relativewater content at turgor loss, and a higher bulk modulus of elasticitythan the following four hosts: the native Kunzea ericoides andCoprosmapropinqua, and the introduced Ribes sanguineum and Teline monspessulana.Water potential at turgor loss (_tlp) was strongly correlatedwith the minimum field water potential of both mistletoes andhosts. When _tlpof mistletoe and host is similar (as on Kunzeaand Ribes) field water potentials are also similar, but when_tlpis lower in the mistletoe (as on Coprosma and Teline), thefield water potential of the mistletoe is lower than that ofits host. Consequently, I. micranthus is likely to be more frequenton hosts that maintain high field water potentials than on hoststhat develop low water potentials. Copyright 1999 Annals ofBotany Company Water relations, water potential, osmotic potential, pressure-volume, Ileostylus micranthus , mistletoe, New Zealand.     

Oxidative stress decreases pHi and Na(+)/H(+) exchange and increases excitability of solitary complex neurons from rat brain slices

Putative chemoreceptors in the solitary complex (SC) are sensitive to hypercapnia and oxidative stress. We tested the hypothesis that oxidative stress stimulates SC neurons by a mechanism independent of intracellular pH (pH_i). pH_i was measured by using ratiometric fluorescence imaging microscopy, utilizing either the pH-sensitive fluorescent dye BCECF or, during whole cell recordings, pyranine in SC neurons in brain stem slices from rat pups. Oxidative stress decreased pH_i in 270 of 436 (62%) SC neurons tested. Chloramine-T (CT), N-chlorosuccinimide (NCS), dihydroxyfumaric acid, and H₂O₂ decreased pH_i by 0.19 ± 0.007, 0.20 ± 0.015, 0.15 ± 0.013, and 0.08 ± 0.002 pH unit, respectively. Hypercapnia decreased pH_i by 0.26 ± 0.006 pH unit (n = 95). The combination of hypercapnia and CT or NCS had an additive effect on pH_i, causing a 0.42 ± 0.03 (n = 21) pH unit acidification. CT slowed pH_i recovery mediated by Na⁺/H⁺ exchange (NHE) from NH₄Cl-induced acidification by 53% (n = 20) in -buffered medium and by 58% (n = 10) in HEPES-buffered medium. CT increased firing rate in 14 of 16 SC neurons, and there was no difference in the firing rate response to CT with or without a corresponding change in pH_i. These results indicate that oxidative stress 1) decreases pH_i in some SC neurons, 2) together with hypercapnia has an additive effect on pH_i, 3) partially inhibits NHE, and 4) directly affects excitability of CO₂/H⁺-chemosensitive SC neurons independently of pH_i changes. These findings suggest that oxidative stress acidifies SC neurons in part by inhibiting NHE, and this acidification may contribute ultimately to respiratory control dysfunction. hyperoxic hyperventilation; O₂ toxicity; pH regulation; brain stem; reactive oxygen species     

Respiration and Carbohydrate Accumulation in the Water-Stressed Wheat Apex

The effect of water stress on the respiration of the immaturefloral apex of wheat was studied in a controlled environmentand related to changes in water relations, growth, protein synthesis,and solute accumulation. Apex respiration measured in vitropolarographically showed no wounding response and was cyanide-and malonate-sensitive. It decreased with each decrease in apexwater potential _a reaching 40% of the non-stress control rateat –5·0 MPa, irrespective of whether the waterstress was induced by droughting in vivo or non-permeating osmoticain vitro. Apex respiration was not quantitatively related toturgor potential. During drought stress there was a conservation of ethanol-insolubledry matter and water in the apex while ethanol-soluble carbohydratesand amino acids accumulated. The calculated daily import ofsoluble carbohydrate into the apex during the whole droughtstress period remained nearly constant despite falling waterpotential. Respiration of the apex during a drought period wasnot limited by the suistrate supply within the apex.     

Simulation and Prediction of Plant Phenology for Five Crops Based on PhotoperiodxTemperature Interaction

This paper presents a plant phenological model based on genotypextemperaturexphotoperiodinteraction (GPTmodel). In the model, rate of development towardsa specified stage (e.g. flowering) for a given genotype is composedof three components: the genotype's maximum rate of development;any delay due to a non-optimal temperature; and any delay dueto a photoperiod response. It is assumed that development tothe specified stage is an autonomous process established bymost, if not all, genes other than the vernalization genes andthe photoperiod genes; and that this autonomous process is delayedby any activity of the photoperiod genes. Since all physiologicalprocesses are modulated by temperature, any photoperiod responseis inevitably a photoperiodxtemperature interaction. This interactionis simulated by assuming that the photoperiod gene activityoccurs only beyond a critical photoperiod (P_c) and is enlargedby temperature above a base temperature (T_bp) that allows thephotoperiod gene activity. The model is written asR=1/D_b-S_t(T-T_opt)²-S_p(T-T_bp)|P-P_c|, whereRis the expected rate of development to the specifiedstage under any combination of temperature (T) and photoperiod(P). The other model parameters are:S_p, the sensitivity to adelaying photoperiod;T_opt, the optimum temperature for developmentin the absence of the photoperiod response;S_t, the sensitivityto a non-optimum temperature; andD_b, the basic duration to thespecified stage (or intrinsic earliness), the inverse of whichis the maximum rate of development.D_bis observable only ifT=T_optandsimultaneouslyP     

Humidity response of cuticular conductance of beech (Fagus sylvatica L.) leaf discs maintained at high relative water content

Cuticular conductance of adaxial (astomatous) and abaxial (stomatous)surfaces ofFagus sylvatica L. leaves was measured under varyingvapour pressure deficits (D). Conductance was determined fromgravimetric measurements of water flux made using a leaf discenvelope specially designed to maintain leaf relative watercontent and minimize reduction in cuticular hydration. The adaxialsurface provided a determination of ‘true’ cuticularconductance (g_c) and transpiration (E_c). The abaxial surfacewas used to estimate minimum leaf surface conductance (g^MIN_sur)and transpiration (E^MIN_sur). In experiment I, leaf discs wereplaced under one of a range of water vapour pressure deficits(0.4-2.0 kPa). Both g_c and g^MIN_sur decreased approximately 2-foldwith an increase in D between 0.4-2.0 kPa. The decrease in g_cwas linear, but g^MIN_sur declined more steeply at D between 0.4-0.95kPa than at D between 0.95-2.0 kPa. In experiment II, leaf discswere exposed to a stepwise change in D. After a period of acclimationto D of 0.95 kPa, responses of g_c and g^MIN_sur to an increaseor decrease in D were recorded. The response time of g_c to increasingor decreasing D were similar (<60 min). By contrast, g^MIN_surresponded more slowly to increasing than to decreasing D. Thesesignificant responses of g_c and g^MIN_sur to increasing and decreasingD are discussed in relation to hydration state of the cuticleand current knowledge of cuticle structure. Key words: Cuticle, cuticular conductance, cuticular membrane, Fagus sylvatica, humidity, vapour pressure deficit     

Adenine nucleotide-creatine-phosphate module in myocardial metabolic system explains fast phase of dynamic regulation of oxidative phosphorylation

Computational models of a large metabolic system can be assembled from modules that represent a biological function emerging from interaction of a small subset of molecules. A "skeleton model" is tested here for a module that regulates the first phase of dynamic adaptation of oxidative phosphorylation (OxPhos) to demand in heart muscle cells. The model contains only diffusion, mitochondrial outer membrane (MOM) permeation, and two isoforms of creatine kinase (CK), in cytosol and mitochondrial intermembrane space (IMS), respectively. The communication with two neighboring modules occurs via stimulation of mitochondrial ATP production by ADP and P_i from the IMS and via time-varying cytosolic ATP hydrolysis during contraction. Assuming normal cytosolic diffusion and high MOM permeability for ADP, the response time of OxPhos (t_mito; generalized time constant) to steps in cardiac pacing rate is predicted to be 2.4 s. In contrast, with low MOM permeability, t_mito is predicted to be 15 s. An optimized MOM permeability of 21 µm/s gives t_mito = 3.7 s, in agreement with experiments on rabbit heart with blocked glycolytic ATP synthesis. The model correctly predicts a lower t_mito if CK activity is reduced by 98%. Among others, the following predictions result from the model analysis: 1) CK activity buffers large ADP oscillations; 2) ATP production is pulsatile in beating heart, although it adapts slowly to demand with "time constant" 14 heartbeats; 3) if the muscle isoform of CK is overexpressed, OxPhos reacts slower to changing workload; and 4) if mitochondrial CK is overexpressed, OxPhos reacts faster. systems biology; computational model; creatine kinase; phosphocreatine shuttle; regulatory module; mitochondrial membrane permeability; oxygen consumption     

Abscisic Acid and Water Relations of Rice (Oryza sativa L.): Sequential Responses to Water Stress in the Leaf

Water stress was imposed by withholding water at an early vegetativestage from plants of two rice cultivars (IR20 and 63–83)grown in pots. As stress intensified the following sequenceof responses of the leaves was observed: (i) rise in abscisicacid (ABA) content, (ii) closure of stomata, (iii) initiationof leaf rolling. In both cultivars, turgor (_p) declined linearly with total waterpotential () of the leaf. Bulk leaf ABA content increased linearlyas _p declined, and attained twice the control (unstressed) levelfollowing a reduction in _p of about 0.12 MPa. Stomatal conductance exhibited a sigmoidal relationship to _p,declining abruptly when a particular ‘critical’_p was reached (threshold response). The critical potentialsvaried considerably between experiments, but were closely correlatedwith control potentials and with the potentials at which ABAconcentration doubled relative to controls. Leaf rolling was initiated at s near to zero _p. Increases inthe ratio of adaxial to abaxial conductance were associatedwith rolling. Variations in the above responses could be accounted for byvariations in the rate of stress development, which in termsof reduction ranged from 0.38 to 0.86 MPa day^–1. Fastdrying rates resulted in: (a) reduced osmotic adjustment, (b)increased amounts of ABA in the leaf at a given level of or_p, (c) an increase in the ABA concentration present at 50 percent stomatal closure, and (d) initiation of leaf rolling ata higher . Oryza sativa L., rice, water stress, stomata, leaf rolling, abscisic acid