The role of solute accumulation, osmotic adjustment and changes in cell wall elasticity in drought tolerance in Ziziphus mauritiana (Lamk.)

Ber (Ziziphus mauritiana Lamk.) is a major fruit tree crop of the north-west Indian arid zone. In a study of the physiological basis of drought tolerance in this species, two glasshouse experiments were conducted in which trees were droughted during single stress-cycles. In the first experiment, during a 13 d drying cycle, pre-dawn leaf water (leaf) and osmotic () potentials in droughted trees declined from -0.5 and -1.4 MPa to -1.7 and -2.2 MPa, respectively, for a decrease in relative water content () of 14%. During drought stress, changes in sugar metabolism were associated with significant increases in concentrations of hexose sugars (3.8-fold), cyclitol (scyllo-inositol; 1.5-fold), and proline (35-fold; expressed per unit dry weight), suggesting that altered solute partitioning may be an important factor in drought tolerance of Ziziphus. On rewatering pre-dawn leaf and recovered fully, but remained depressed by 0.4 MPa relative to control values, indicating that solute concentration per unit water content had changed during the drought cycle.Evidence for osmotic adjustment was provided from a second study during which a gradual drought was imposed. Pressure-volume analysis revealed a 0.7 MPa reduction in osmotic potential at full turgor, with leaf at turgor loss depressed by 1 MPa in drought-stressed leaves. Coupled with osmotic adjustment, during gradual drought, was a 65% increase in bulk tissue elastic modulus (wall rigidity) which resulted in turgor loss at the same in both stressed and unstressed leaves. The possible ecological significance of maintenance of turgor potential and cell volume at low water potentials for drought tolerance in Ziziphus is discussed.Keywords: Ziziphus mauritiana, drought, solute accumulation, osmotic adjustment, proline.      

Foliar dehydration tolerance of twelve deciduous tree species

The potential for foliar dehydration tolerance and maximum capacity for osmotic adjustment were compared among 12 temperate, deciduous tree species, under standardized soil and atmospheric conditions. Dehydration tolerance was operationally defined as lethal leaf water potential (); the of the last remaining leaves surviving a continuous, lethal soil drying episode. Nyssa sylvatica Marsh., and Liriodendron tulipifera L. were most sensitive to dehydration, having lethal leaf of -2.04 and -2.38 MPa, respectively. Chionanthus virginicus L., Quercus prinus L., Acer saccharum Marsh., and Quercus acutissima Carruthers withstood the most dehydration, with leaves not drying until leaf dropped to -5.63 MPa or below. Lethal leaf (in MPa) of other, intermediate species were: Quercus rubra L. (-3.34), Oxydendrum arboreum (L.) D.C. (-3.98), Halesia carolina L. (-4.11), Acer rubrum L. (-4.43), Quercus alba L. (-4.60), and Cornus florida L. (-4.88). Decreasing lethal leaf was significantly correlated with increasing capacity for osmotic adjustment. C. virginicus and Q. acutissima showed the most osmotic adjustment during the lethal soil drying episode, with osmotic potential at full turgor declining by 1.73 and 1.44 MPa, respectively. Other species having reductions in osmotic potential at full turgor exceeding 0.50 MPa were (in MPa) Q. prinus (0.89), A. saccharum (0.71), Q. alba (0.68), H. carolina (0.67), Q. rubra (0.60), and C. florida (0.52).     

Optimization theory of stomatal behaviour II. Stomatal responses of several tree species of north Australia to changes in light, soil and atomospheric water content and temperature

In a companion paper several methods of calculating the marginal unit water cost of plant carbon gain (E/A) were tested to determine whether stomata were behaving optimally in relation to regulating leaf gas exchange. In this paper one method is applied to several tropical tree species when leaf-to-air vapour pressure difference (D), photosynthetic photon flux density, leaf temperature, and atmospheric soil water availability were manipulated. The response of leaves that had expanded during the dry season were also compared to that of leaves that had expanded in the wet season. Few differences in absolute value of E/A, or the form of the relationship, were observed between species or between seasons. In the majority of species, E/A increased significantly as either leaf-to-air vapour pressure difference increased, at a leaf temperature of either 33C or 38C, or as in photosynthetic photon flux density increased. In contrast, as leaf temperature increased at constant D, E/A was generally constant. As pre-dawn water potential declined, E/A declined. The relationship between E/A and D did not differ whether internal or ambient carbon dioxide concentration were kept constant. It is concluded that stomata are only behaving optimally over a very small range of D. If a larger range of D is used, to incorporate values that more closely reflect those experienced by tropical trees in a savanna environment optimization is incomplete.Key words: Stomatal optimization theory, marginal unit water cost.      

Plant Growth in Polyethylene Glycol Solutions in Relation to the Osmotic Potential of the Root Medium and the Leaf Water Balance

The changes in leaf extension, plant dryweight, leaf area, netassimilation rate (E), relative growth-rate (R_W), and relativeleaf growth-rate (R_L), have been studied for four species grownfor 2 weeks in solutions of polyethylene glycol 4000 of controlledosmotic potentials. All aspects of growth were decreased bydecreasing the osmotic potential (_sol) of the root medium andthe leaf water potential (), and ceased when _/ was greater than— 10 bars in bean, cotton, maize. These plants were moresusceptible than ryegrass to water stress. Growth of bean stoppedat equal to about —6 bars, but even at —10 barsryegrass was capable of some growth. Slight decrease in fromthe values in the control plants decreased growth during thefirst week but partial recovery was apparent during the secondweek's growth in solution culture, when leaf extension, E, R_Land R_W increased in plants subjected to stress. Examinationof the water balance, water potential, osmotic potential andturgor of the leaf in relation to relative water content suggeststhat recovery was related to increased turgor and that the abilityof the plants to grow at reduced values of the osmotic potentialof the root medium and of the leaf water potential depend onthe maintenance of turgor.     

Alternative Methods of Analysing Water Potential Isotherms: Some Cautions and Clarifications: I. THE IMPACT OF NON-IDEALITY AND OF SOME EXPERIMENTAL ERRORS

In recent years alternative ways have been proposed to transformmeasurements of leaf water potential, , and relative water content,R^*, in order to derive values of osmotic pressure at full turgidityin leaves and shoots, ^o(when 0). Two types of transformationsare usually considered: 1/ versus R^* and versus 1/R^*, and linearregression is used to fit the data in the region where turgoris thought to be zero. It appears that when ^o is estimated bylinear extrapolation of 1/Psi; versus R^* then apoplastic watermight not influence the accuracy of ^o but when the versus \/R^*transformation is used apoplastic water causes an underestimateof ^o. We examine the accuracy of the estimate of ^o obtainedfrom the two transformations when there are random errors in, systematic errors in , and when the osmotic solutions arenon-ideal. The 1/ versus R^* transformation generally producesthe best estimate of ⁰ by linear extrapolation.     

Mechanisms of Inhibition of Water Movement in Anaerobically Treated Roots of Zea mays L.

Changes in water flux (Jv) across detopped, 7-d-old, maize rootswere characterized during the initial 24 h of being made anoxicby exposure to an anaerobic nutrient solution. Suction (50 kPa)was applied to the xylem and samples of the xylem sap were collectedat intervals and the osmolality and ionic content were measured. Values of Jv through anoxic roots fell below those of aerobiccontrols 1 h after the equilibrium oxygen partial pressure inthe bathing medium dropped below 20 kPa (air = 20.6 kPa). Thereduction in Jv was due primarily to a nullification of thediurnal rhythm in hydraulic conductivity (Lp) that was measuredin aerobic roots. However, about one-quarter of the reductionin Jv could be accounted for by a smaller osmotic componentof the driving force () on water movement. The significance of changes in Jv in anoxic roots is discussedin terms of the reliability of estimates of Lp, the reflectioncoefficient () and . Key words: Anaerobiosis, hydraulic conductivity, osmotic potential, water     

Cyclic Variations in Nitrogen Uptake Rate of Soybean Plants: Effects of External Nitrate Concentration

Net uptake of by non-nodulated soybean plants [Glycine max (L.) Merr.cv. Ransom] growing in flowing hydroponiccultures containing 0–5, 1.0 and 10-0 mol m^–3 was measured daily during a 24-d period of vegetativedevelopment to determine if amplitude of maximum and minimumrates of net uptake are responsive to external concentrations of . Removal of from the replenished solutions during each 24-h period was determinedby ion chromatography. Neither dry matter accumulation nor theperiodicity of oscillations in net uptakerate was altered bythe external concentrations. The maxima of the oscillations in net uptake rate, however, increased nearly3-fold in response to external concentrations. The maxima and minima, respectively, changed from 4.0 and 0–6mmol per gram root dry weight per day at an external solution level of 05 mol m^–3 to 15–2and -2–7 mmol per gram root dry weight per day at an external solution level of 10–0mol m^–3 . The negative values for minimum net uptake rate from10–0 mol m^–3 solutions show that net efflux was occurring andindicate thatthe magnitude of the efflux component of net uptake was responsiveto external concentration of . Key words: Nitrate uptake rate, carbon-nitrogen partitioning, flowing solution culture     

N2 Fixation (C2H2-Reducing Activity) and Leghaemoglobin Content during Nitrate- and Water-Stress-Induced Senescence of Medicago sativa Root Nodules

Nitrate and water stress were used to induce senescence in rootnodules of alfalfa (Medicago sativa L. cv. Aragon). Nodule senescencewas assessed by determinations of the nitrogenase (C₂H₂-reducing)activity, and the leghaemoglobin (LHb) and total soluble proteincontents of the nodules. Nodules responded similarly to and water stress in many respects, but there was a significant difference.All parameters of nodule activity, expressed on the basis ofnodule dry weight (DW), consistently decreased following treatmentwith or during drought; there was a significant interaction (synergism) between the inhibitory effects of and water stress on nitrogenase activity, but sucheffects were merely additive in the case of LHb content or LHb/solubleprotein ratio. However, caused the selective decay of LHb with respect to other nodular soluble proteins,whereas the decrease of LHb during water stress was due to ageneral inhibition of protein synthesis and to an increasedproteolytic activity in the nodule cytosol rather than to aspecific proteolysis of LHb. Key words: Leghaemoglobin, Medicago saliva, nitrogen fixation, root nodule senescence, water stress     

Stomatal Response to Water Stress and its Relationship to Bulk Leaf Water Status and Osmotic Adjustment in Pearl Millet (Pennisetum americanum [L.] Leeke)

The water potential () at which stomata completed closure (_8Lmin)was determined for pearl millet (Pennisetum americanum [L.]Leeke) at two growth stages by monitoring changes in leaf conductance(g_L) and following shoot detachment. Leaf water status wasevaluated concurrently using a pressure-volume (P-V) technique. In a pot experiment with young vegetative plants, _8Lmin closelyapproximated to the estimated at zero turgor (_u) both for controland for drought-conditioned plants which had osmotically adjusted.However, for penultimate leaves of field-grown flowering plants,_8Lmin was found to be 0.61 (irrigated plants) and 0.87 (droughtedplants) MPa below _u. In drought-stressed field-grown plants,osmotic adjustment (characterized by a decrease in solute (osmotic)potential (_s ) at both full hydration and zero turgor) was insufficientto maintain a positive bulk leaf turgor potential (_p) once had declined to below about -1.5 MPa. It is suggested that localizedadjustment by the stomatal complex in response to environmentaldifferences, leaf ageing and/or ontogenetic change, is responsiblefor the uncoupling of stomatal from bulk leaf water status. Key words: Stomata, Water stress, Pennisetum americanum     

A simulation model to predict seed dormancy loss in the field for Bromus tectorum L

Bromus tectorum L. (cheatgrass) is an invasive winter annual whose seeds lose dormancy through dry after-ripening. In this paper a thermal after-ripening time model for simulating seed dormancy loss of B. tectorum in the field is presented. The model employs the hydrothermal time parameter mean base water potential (b(50)) as an index of dormancy status. Other parameters of the hydrothermal time equation (the hydrothermal time constant HT, the standard deviation of base water potentials b, and the base temperature Tb) are held constant, while b(50) is allowed to vary and accounts for changes in germination time-course curves due to stage of after-ripening or incubation temperature. To obtain hydrothermal time parameters for each of four collections, seeds were stored dry at 20C for different intervals, then incubated in water (O MPA) or polyethylene glycol (PEG) solutions (-0.5, -1.0, -1.5 MPa) at 15 and 25C. Germination data for the thermal after-ripening time model were obtained from seeds stored dry in the laboratory at 10, 15, 20, 30, 40, and 50°C for 0 to 42 weeks, then incubated at two alternating temperatures in water. Change in b(50) was characterized for each collection and incubation temperature as a linear function of thermal time in storage. Measurements of seed zone temperature at a field site were combined with equations describing changes in b(50) during after-ripening to make predictions of seed dormancy loss in the field. Model predictions were compared with values derived from incubation of seeds retrieved weekly from the field site. Predictions of changes in b(50) were generally close to observed values, suggesting the model is useful for simulating seed dormancy loss during after-ripening in the field.     

Physiological and morphological responses to elevated CO2 and a soil moisture deficit of temperate pasture species growing in an established plant community

Periods of limited soil water availability are a feature of many temperate pasture systems and these have the potential to modify pasture plant and community responses to elevated atmospheric CO2. Using large pasture turves, previously exposed to elevated CO2 concentrations of 350 or 700 mol mol^-1 for 324 d under well-watered conditions the morphological and physiological responses of pasture species growing at these CO2 concentrations were compared when subjected to a soil moisture deficit-and to recovery from the deficit-with those that continued to be well watered.Net leaf photosynthesis of Trifolium repens (C3 legume), Plantago lanceolata (C3) and Paspalum dilatatum (C4) was increased by exposure to elevated CO2, but there was no consistent effect of CO2 on stomatal conductance. At low soil moistures, net photosynthesis declined and stomatal conductance increased in these three species. There was a strong CO2 x water interaction in respect of net photosynthesis; in Trifolium repens, for example, elevated CO2 increased net photosynthesis by approximately 50% under well-watered conditions and this increased to over 300% when soil moisture levels reached their minimum values. Similar values were recorded for both Paspalum dilatatum and Plantago lanceolata. Potential water use efficiency (net photosynthesis/stomatal conductance) was increased by both exposure to elevated CO2 and drought.Leaf water status was measured in three species: Trifolium repens, Paspalum dilatatum and Holcus lanatus (C3). Total leaf water potential (t) and osmotic potential () were decreased by drought, but CO2 concentration had no consistent effect. t and were highest in the C4 species Paspalum dilatatum and lowest in the legume Trifolium repens.In the wet turves, rates of leaf extension of the C3 grasses Holcus lanatus and Lolium perenne at elevated CO2 were frequently higher than those at ambient CO2, but there was no effect of CO2 concentration on the rate recorded in the C4 grass Paspalum dilatatum or the rate of leaf appearance in the legume Trifolium repens. Drought reduced leaf extension rate irrespective of CO2 in all species, but in Holcus lanatus the reduction was less severe at elevated CO2. Immediately after the dry turves were rewatered the leaf extension rate on tillers of Holcus lanatus and Lolium perenne were higher than on tillers in the wet turves, but only at ambient CO2. Consequently, despite the greater leaf extension rate during the soil moisture deficit at elevated CO2, because of the overcompensation after rewatering at ambient CO2, total leaf extension over both the drying and rewetting period did not differ between CO2 concentrations for these C3 grass species. Further investigation of this difference in response between CO2 treatments is warranted given the frequent drying and wetting cycles experienced by many temperate grasslands.     

Derivation of Pressure-Volume Curves by a Non-Linear Regression Procedure and Determination of Apoplastic Water

Data from pressure-volume (PV) analysis may be submitted totransformation I [i.e. leaf water potential (₁) versus inverserelative water content (1/R)] or to transformation II (i.e.1/₁ versus R). This may cause an essential distortion of theerror structure especially in transformation II due to the relativelylarge range which is to be covered by the 1/₁ ratio. Similarly,logarithmic transformation of leaf turgor potential (_P) whenderiving the sensitivity factor of elasticity (ß)by linear regression from values of In _p and 1/R may distortthe error structure. In order to investigate the magnitude ofthe distortion effect on parameters derived from PV analysisby regression a non-linear regression procedure was comparedwith the common linear procedure when calculating _p from ßin the turgid region and leaf osmotic potential (_P) in boththe turgid and non-turgid region. As test plants we used fieldgrown species of spring barley (Hordeum distichum L., cvs Gunnarand Alis). The results show that transformations and applicationof linear regression procedures distort the error structureof _p more than the error structure of _', which was only slightlyaffected. However, we recommend the use of the non-linear procedurein both cases. Furthermore, from PV analysis, obtained by thermocouple hygrometryon living and killed leaf tissue, respectively, we derived themathematical basis for calculating the apoplastic water fraction(R_a). R_a was 0.15 at R= 1 and decreased with dehydration. The equations describing the relation between and R and between_p and R were extended to take into account the apoplastic waterfraction. Key words: Apoplastic water, distortion errors, non-linear regression, pressure-volume curves     

The Meaning of Matric Potential

The commonly used equation, = P - + , which describes thepartitioning of plant water potential, , into components ofhydrostatic pressure, P, osmotic pressure, , and matric potential,, is misleading. The term , which is supposed to show the influenceof a solid phase on , is zero if a consistent definition ofpressure is used in the standard thermodynamic derivation. However,it can be usefully defined by = + _D, where _D is the osmoticpressure of the equilibrium dialysate of the system. The practicaland theoretical significance of this definition is discussed.     

Developmental Responses to Drought and Abscisic Acid in Sunflower Roots: I. ROOT GROWTH, APICAL ANATOMY, OSMOTIC ADJUSTMENT

Aeroponically grown sunflower seedlings (Helianthus annuus L.cv. Russian Giant) were droughted or treated with abscisic acid(ABA) for 7 d. Drought stress prompted a three-phase growthresponse in sunflower roots: an initial phase of increased rootelongation was followed by a period of almost complete inhibitionbetween about 6 h and 72 h; this was followed, in turn, by aphase of partial recovery in the rate of root elongation. Droughtdecreased the size of the apical meristem as cells in the proximalregion of the meristem vacuolated and elongated. Root-to-shootbiomass ratios (R:S) increased initially but declined after72 h. Drought stress decreased water potential () and osmoticpotential ( and increased turgor pressure _p in the apical 30mm of the roots. These initial changes were transitory, lastingabout 3 h. Thereafter, and began to rise; _p fell back to controllevels. In the later stages of treatment, fell as the stressgrew more severe, but fp was maintained by osmotic adjustment.Desiccation for 1 h increased turgor pressures in excised 30mm apical segments. The transitory increase in root elongationwas contemporary with the initial rise in _p in the root apices,while the periods of greatest inhibition and partial recoveryin root elongation were contemporary with the periods of declineand partial recovery in the length of the apical meristem respectively.The inhibition of root elongation and the anatomical changesin the root apices were not determined by loss of turgor orlack of photosynthate, but rather appeared to be an active responseby the meristem to a drop in external . Treatment with ABA triggeredmany of the same changes as drought stress: ABA promoted a three-phasegrowth response, increased R:S, triggered the same initial changesin , , and _p, increased _p in excised 3.0 mm apical segments,and induced the same pattern of anatomical changes in the rootapices as drought stress. It is proposed that ABA mediates drought-inducedchanges in the primary development of sunflower roots. Key words: Abscisic acid, apical meristem, drought, osmotic adjustmen     

Adaptation of the Euryhaline Charophyte Lamprothamnium papulosum to Brackish and Freshwater: Turgor Pressure and Vacuolar Solute Concentrations During Steady-State Culture and After Hypo-osmotic Treatment

The euryhaline charophyte Lamprothamnium papulosum (Wallr.)J. Gr. was adapted to media with decreasing salinities rangingfrom 550 to 0 mosmol kg^–1. Vegetative plants grown inmedia with osmotic pressures (⁰) in the range of 550 to 130mosmol kg^–1 maintained a constant turgor pressure () at309 + 7 mosmol kg^–1. The ions K+, Na+ and Cl–, werethe predominant solutes in the vacuole. Changes in their concentrationsaccount for the variation in internal osmotic pressure (¹) with,⁰. The divalent ions Mg²⁺, Ca²⁺ and were also present in significant amounts, but their concentrationsdid not alter with changes in, ⁰. In cells subjected to hypo-osmotic shock the regulation of was incomplete. The turgor pressure increased from 302 to 383mosmol kg^–1. The first rapid response to the sudden decreasein ⁰ was a loss of K⁺ and Cl^–. In contrast to the decreasein ionic concentrations an accumulation of sucrose occurredwhich could account for the increase of . The increase in sucroseconcentration started 24 to 48 h after the downshock and reachedits highest value after 3 to 4 weeks. The sucrose concentrationin the vacuole was up to 320 mol m^–3. During this timethe ionic content continued to decrease but did not counterbalancethe sucrose concentration sufficiently to regain the original. High sucrose levels accompanied by an enhanced were also observedduring the period of fructification (sexual reproduction: formationof antheridia and oogonia) in Lamprothamnium kept under conditionsof constant salinity. It is concluded that high sucrose content and elevated arecharacteristic of sexual reproduction in this charophyte. Lamprothamniumis able to tolerate different during various developmentalstages (e.g. vegetative and reproductive phases). Key words: Lamprothamnium papulosum, sucrose, turgor pressure     

The Derivation of the Cell Wall Elasticity Function from the Cell Turgor Potential

An equation is derived expressing average turgor pressure ofa leaf (_p) as a function of relative water content (RWC). Basedon this derivation, the relationships of the bulk elastic modulus(_v) and both RWC and _p, are formulated and discussed. The bulkelastic modulus (_v) becomes zero for _p = 0, that is at the turgorloss point for the leaf. At full water saturation the valueof ev is proportional to the water saturation turgor potential_p(max). The factor relating _P and _v (structure coefficient ,Burstrom, Uhrstr?m and Olausson, 1970) changes only very littlefor values of _p, which are not too close to zero. An exampleis given for the calculation from experimental data of the turgorpressure function, the structure coefficient function, and the_v function. Key words: Cell wall, Turgor pressure, Bulk elastic modulus     

Hydrothermal time analysis of tomato seed germination responses to priming treatments

Controlled hydration of seeds followed by drying (seed priming) is used to break dormancy, speed germination, and improve uniformity of radicle emergence. To date, empirical trials are used to predict optimal priming conditions for a given seed lot. Since priming is based upon seed water relations, it was hypothesized that the sensitivity of germination to reduced water potential before priming might be mechanistically related to, and therefore predictive of, priming responsiveness. Analyses of germination of 13 tomato (Lycopersicon esculentum Mill.) seed lots at two temperatures (15C and 20C) and three water potentials (0, -0.28 and -0.43 MPa) showed that seed lot germination responses could be quantitatively characterized by parameters derived from thermal time, hydrotime, and hydrothermal time models (R²0.73-0.99). Six of the seed lots were primed at two temperatures (15°C and 20°C) and three water potentials (-1.0, -1.5 and -2.0 MPa) for various durations, dried, and their subsequent germination rates analysed according to hydropriming time and hydrothermal priming time models. The responses of germination rates to priming were characterized by hydropriming time (HP) and hydrothermal priming time (HTP) constants and the minimum water potential (min) and temperature (Tmin) for achieving a priming effect. The values of min and Tmin varied relatively little among tomato seed lots, and the generalized values of min=2.39 MPa and Tmin=9.10°C accounted for 74% (15°C), 57% (20°C), and 62% (across both temperatures) of the increase in germination rates following priming. Nonetheless, while the hydrothermal time models described germination patterns both before and after priming, there was relatively little predictive relationship between them.     

Gene note. Characterization of a tomato karyopherin {alpha} that interacts with the Tomato Yellow Leaf Curl Virus (TYLCV) capsid protein

A karyopherin (LeKAP1) cDNA was isolated from tomato plants. The deduced LeKAP1 protein sequence of 527 amino acids showed similarity to other plant karyopherin proteins. When LeKAP1 was expressed in a yeast two-hybrid system together with the gene coding for the capsid protein (CP) of the tomato yellow curl leaf virus (TYLCV), it interacted directly with CP. Thus, LeKAP1 may be involved in the nuclear import of TYLCV CP and, potentially, the TYLCV genomes during viral infection of the host tomato cells.     

Short communication. A steep Ca2[IMAGE]-dependence of a K[IMAGE] channel in a unicellular green alga

An increase of cytosolic Ca² in the unicellular green alga Eremosphaera viridis activities Ca²-dependent K channels causing a hyperpolarization of the plasma membrane. Data from parallel calcium, and potential measurements were combined with I/V relationships. This yielded a steep Ca²-dependence of K channels with a co-operativity of 4 and an affinity of 300 nM.Key words: Eremosphaera viridis, plasma membrane, Ca²-dependent K channel, co-operative binding.      

Nitrate Uptake and Assimilation following Nitrate Deprivation

Upon first exposure to , the uptake and reduction capacities of dark-grown corn (Zea maysL.) roots are initially low, but increase markedly within 6h. The development of the accelerated uptake rate appears to be substrate ‘induced’ as is reductase (NR), the first enzyme in the assimilatory pathway. However, the ‘induction’of uptake is independent of NR induction. The effect of deprivation was studied to determine the role of endogenous on subsequent uptake and reduction. Corn roots were ‘induced’ for 24 h in 0–5 mol m^–3 nutrient solution and then exposed for 0 to 32 h to -free nutrient solution. Uptake and reduction of were determined periodically by exposing sets of roots to a1 h pulse of 0.5 mol m^–3 . Neither uptake (4.57 µmol root^–1 h^–1)nor the percentage of absorbed reduced (27%) was changed significantly (P 0.05) by exogenous deprivation. However, the estimated ‘induced’ componentof uptake decreased significantly (50% after 32 h). Concurrently, the ‘non-induced’ basal componentof uptake increased. Previously accumulated decreased from 23 to 4.5 µmol root^–1 after 32 h of exogenous deprivation. Nearly equivalent quantities of endogenous were used for translocation and reduction during deprivation. During each 1 h pulse, the amounts of translocation and net efflux of to the uptake solution were similar. Net efflux of was strongly correlated (r = 0.991) to the amount of endogenous . The remaining endogenous and its rate of utilization were apparently sufficient to minimize a rapid declineor complete loss in both the ‘induced’ uptake state and the rate of in vivo assimilation. Key words: reduction, translocation, efflux, root, Zea mays L