The Dependence of Net Assimilation Rate on Leaf-area Index

The leaf-area index (leaf area per unit area of land, L) offield crops of kale and sugar-beet was varied experimentallyby removing different fractions of the plant population distributeduniformly through the crop. The net assimilation rate (E) wasdetermined in subsequent periods of 10–14 days. For kale, E decreased nearly linearly with increase of L throughoutthe range from I to 5. E of sugar-beet was less affected bychange in L and was apparently not decreased until L rose aboveabout 3. Because of this dependence of E on L, the rate of dry-matterproduction per unit area of land, or crop growth-rate (C=EL),showed a curved relation to L; for kale it increased to a maximumwhen L was between 3 and 4 and fell again at higher values ofL. Maximal C for sugar-beet occurred beyond the range of L tested,probably between L=6 and L=9. This optimal L for dry-matterproduction by sugar-beet crops probably lies near the upperlimit of the current agricultural range, so there is little,if any, scope for increasing the dry-matter yield by furtherincrease in L. For heavy kale crops L is already far in excessof the optimum, and it may be possible to increase the totaldry-matter yield of kale by repeated thinning or defoliationto hold L near the optimum.     

Effects of Age and Environment on Net Assimilation Rate of Barley

To distinguish between the effects of age and environment onnet assimilation rate (E) of barley (var. Brant) grown in theopen in pots at Ottawa, E was measured outdoors (treatment N)and on similar plants transferred to a constant environmentfor the 2 weeks during which E was determined (treatment T).During June and July, E of treatment N decreased by 77 per cent.;for treatment T this fall increased to 90 per cent, of the initialvalue. E and average day and night temperatures were greaterin the constant environment than outdoors in early June, andin July they were greater outdoors. Incident light energy wasalways greater outdoors. Thus, the fall in E with age was partiallymasked outdoors by an increase caused by the improvement inenvironmental conditions during the experiment. Plants grown continuously in the constant environment had lowerE, greater leaf area and dry weight, and ears emerged earlierthan plants of similar age that had been transferred for 2 weeksto the constant environment from outdoors. E of plants growncontinuously in the constant environment decreased with time,both when the pots were moved away from the light panel to maintaina constant light intensity at the base of the youngest leafand when the pots remained stationary so that the plants grewtowards the lights. After ears emerged, E for treatments N and T was measured onplants whose ears were shaded to prevent them photosynthesizing.Photosynthesis in the ear accounted for 19 per cent, of thefinal ear dry weight during the first 2 weeks after emergence,12 per cent, during the 3rd and 4th, and 3 per cent, duringthe 5th and 6th weeks. Shading had no effect on weight of plantparts other than ears and had similar effects outdoors and inthe constant environment.     

Dependence of Net Assimilation Rate on Root Growth of Isolated Leaves

The phenomenon of inhibition of assimilation by carbohydrateaccumulation has been reinvestigated using single rooted leavesof dwarf bean. Such a system has the advantage that assimilatingarea remains constant and carbohydrate is translocated to asingle sink-the root system. The net assimilation rate of thesystem did not vary with season and was small compared withintact plants in the summer, suggesting that an internal factorcontrols assimilation rate. Evidence is given that this factoris the rate of translocation of carbohydrate from source tosink (from lamina to root) which in turn depends on growth-rateof the root system. The evidence came from experiments in whichroot growth was stimulated by increasing vessel size, by preliminarytreatment with IAA or by raising the root temperature, or wasretarded by kinetin treatment. In experiments at glasshouse temperature, lamina dry matterincreased by 0.75 mg. per cm.² per week. The maximum valuesattained depended on the time of the experiment. In August itwas greater than 7.0 mg. per cm.¹, but there was a seasonaltrend. In experiments with roots at 24?C, carbohydrate accumulatedin the lamina more slowly than at lower temperatures.     

The Influence of Removing Tubers on Dry-matter Production and Net Assimilation Rate of Potato Plants

To study the effect of removing tubers on growth and net assimilationrate (E) of potato, plants were grown in pots partly filledwith soil with the shoot growing through a polythene cover.Tubers developed in the space between the cover and the soilsurface. Removing tubers immediately they began to form had little effecton E at the beginning of the experiment but later greatly reducedit. Shading reduced E more at the beginning of the experimentthan later. Removing tubers decreased total dry weight, butmuch of the material that would have moved to tubers accumulatedin leaves and stems. In intact plants the loss of weight byshading was mainly from the tubers; in plants without tubersit was mainly from stems and leaves. Removing tubers increasedleaves on lateral stems. Increasing the amount of nitrogen supplieddiminished the effect on E of removing tubers, presumably becausethe extra allowed other sinks for carbohydrate to develop. Thegrowth of some buds of the potato plant is so strongly inhibitedthat they cannot grow and act as sinks for excess carbohydratewhen tubers are removed. Such internal inhibition of growthmay sometimes suffice to influence the magnitude of E of normalplants. Removing tubers usually increased sugar and starch contentand protein N content of stems and leaves.     

Net Assimilation Rate Determines the Growth Rates of 14 Species of Subtropical Forest Trees

Growth rates are of fundamental importance for plants, as individual size affects myriad ecological processes. We determined the factors that generate variation in RGR among 14 species of trees and shrubs that are abundant in subtropical Chinese forests. We grew seedlings for two years at four light levels in a shade-house experiment. We monitored the growth of every juvenile plant every two weeks. After one and two years, we destructively harvested individuals and measured their functional traits and gas-exchange rates. After calculating individual biomass trajectories, we estimated relative growth rates using nonlinear growth functions. We decomposed the variance in log(RGR) to evaluate the relationships of RGR with its components: specific leaf area (SLA), net assimilation rate (NAR) and leaf mass ratio (LMR). We found that variation in NAR was the primary determinant of variation in RGR at all light levels, whereas SLA and LMR made smaller contributions. Furthermore, NAR was strongly and positively associated with area-based photosynthetic rate and leaf nitrogen content. Photosynthetic rate and leaf nitrogen concentration can, therefore, be good predictors of growth in woody species.     

Influence of Tops and Roots on Net Assimilation Rate of Sugar-beet and Spinach Beet and Grafts between them

Sugar-beet has a larger storage root and greater net assimilationrate (E) than spinach beet. To determine whether the greaterroot was a result or cause of the greater E, grafts were madebetween tops and roots of sugar-beet and spinach-beet in allfour possible combinations. Grafted plants with sugar-beet roots had greater E and rootdry weight, less leaf area and top dry weight and lower concentrationof sugar in the leaf lamina, than those with spinach-beet roots,irrespective of the type of top. Grafted plants with sugar-beettops had greater E, total and root dry weight, but less leafarea, than those with spinach-beet tops, irrespective of thetype of root. The difference in E between grafted plants withsugar-beet tops and spinach-beet tops was similar to that betweengrafted plants with sugar-beet roots and spinach-beet roots.It increased with time to 60 per cent. Increases in E probably represent increases in rate of photosynthesis.Sugar-beet roots probably increased photosynthesis by providinga better sink for assimilates than spinach-beet roots.     

Effects of Seasonal Variation in Radiation and Temperature on Net Assimilation and Growth Rates in an Arid Climate

The net assimilation rate (E_A), relative growth-rate (R_w), andleaf-area ratio (F_A) were measured for rape (Brassica napus),sunflower (Hetianthus annuus), and maize (Zea mays) at varioustimes of year in an arid climate, using young plants grown widelyspaced on nutrient culture. Multiple regression analysis accountedfor 90–95 per cent of the variation in E_A and R_W in termsof two climatic variables: mean temperature and radiation receipt. E_A rose linearly with radiation in all three species; increasein E_A with temperature was greatest in maize and least (notsignificant) in rape. R_Wrose with radiation and temperature,the latter being the more important variable especially in coolweather; a temperature optimum was shown at 24° C in rape.F_A rose with increase in temperature or decrease in radiation;its variation was due to change in leaf area/leaf weight ratherthan in leaf weight/plant weight. Multiple regression analyses can lead to faulty interpretationif the independent variables are correlated (as are climaticvariables in nature), but conclusions can be checked by controlled-environmentstudies in which climatic factors are not correlated. The presentconclusions are supported by such studies. The regression equations, coupled with average weather records,indicate seasonal cycles of growth parameters. E_A is maximalnear midsummer and minimal near midwinter, following the radiationcycle. Maxima and minima in R_W are about a month later, becauseR_W is affected by the temperature cycle and this lags behindthe radiation cycle. F_A is maximal in autumn and minimal inspring. E_A is highest where radiation receipts near 750 cal cm^–2day^–1 coincide with high temperatures. This combinationoccurs only in clear midsummer weather at low latitudes, andis maintained over long periods only in arid regions. The fact that E_A rose linearly with radiation suggests thatleaf water deficits arising under high radiation had littleeffect on E_A and that saturating levels of light were very high.     

Effects of (2 Chloro-Ethyl) Trimethlammonium Chloride on Plant Growth, Leaf Area, and Net Assimilation Rate

Both under glasshouse conditions and in a constant environmentwith light from fluorescent tubes, mustard plants' treatmentwith (2 chloro-ethyl) trimethylammonium chloride (CCC) respondedby an increase in total leaf area. In the glasshouse the increasewas due to the production of more lateral leaves, and in thegrowth chambers to the enlargement of stem leaves, since lateralbranches did not form. Despite the increase in area, the netassimilation rate fell; this may be attributable to an effectof CCC on the photosynthetic mechanism or to an increase inthe mutual shading of leaves, but it is more probable that theinhibition of stem growth also caused by CCC decreases the demandfor photosynthate and leaves photosynthesise less. The leafarea of mustard (a long-day plant) is increased also by short-daytreatment, and here again there is a concomitant shorteningof the stem. Chlorophyll content, both per leaf and per unit area, and totaldry matter per unit area, were increased in tobacco plants grownin culture solutions containing CCC. The treatment affectedthe distribution of nitrogen, increasing the amount per leafand decreasing it per stem.     

Changes in Net Assimilation Rate and Leaf-area Ratio with Time in Dactyl is glomerata L.

Two natural populations of Dactylis glomerata, one from Norwayand the other from Portugal, were grown at four temperaturesin a 16-h photoperiod. Seedlings were harvested at six equalintervals of 7 days at 5 and 10 °C, and 3.5 days at 20 and30 °C. Time curves of net assimilation rate (NAR), leaf-arearatio (LAR) and other growth attributes were derived from curvesfitted to loge leaf area and loge plant weight as functionsof time. Three types of curves were found for both NAR and LARand these conformed to theoretical expectations. There was ageneral decline in NAR and LAR with time, but in certain treatmentsNAR increased during the later harvests, and the possible reasonsfor this are discussed. A similar rise in NAR was also obtainedin an experiment with 12 harvest times.     

The Effect of Manganese on the Assimilation and Respiration Rate of Isolated Rooted Leaves

The effect of manganese on carbon assimilation, respiration,and translocation has been studied using isolated rooted potatoleaves and small potato plants. Methods are described for therooting and culture of the leaves and plants. It was found thatnormal potato leaves rooted readily when treated with -naphtha-leneaceticacid (2 p.p.m.), but that very few of the manganese-deficientleaves produced roots, the critical level being about 15 p.p.m.manganese on a dry weight basis. The growth of isolated deficientleaves was also much less than that of control leaves, but inno case did characteristic manganese-deficiency symptoms develop,although the manganese level had fallen below that of leaveswhich showed symptoms when attached to the plant. A marked differencein net assimilation rate was found between leaves which hada high or low manganese content at the time of rooting. Theaddition of manganese after rooting to low manganese leavesdid not, however, cause an increase in assimilation rate, althoughthe manganese content of the leaves had been raised to thatof the control leaves. Manganese was shown to have only a smalleffect on respiration, higher respiration rate being consistentlyassociated with a higher manganese content; the addition ofmanganese to ‘deficient’ leaves did not cause anyincrease in respiration. No effect of manganese on translocationwas detected.     

水分亏缺对冬小麦净光合速率影响程度研究

水分亏缺对冬小麦净光合速率影响程度研究王慧（西北大学城市与资源学系,西安７１００６９）ＥｆｆｅｃｔｏｆＷａｔｅｒＤｅｆｉｃｉｔｏｎＮｅｔＰｈｏｔｏｓｙｎｔｈｅｓｉｓＲａｔｅｏｆＷｉｎｔｅｒＷｈｅａｔ．ＷａｎｇＨｕｉ（ＤｅｐａｔｍｅｎｔｏｆＵｒｂａｎ...     

The Net Assimilation Rates of Wild and Cultivated Beets

The net assimilation rate (E) of Kleinwanzleben sugar-beet wasthe same as that of three types of wild sea-beet (Beta vulgarissubsp. maritima) when the leaf-area index (L) was near to I.In a subsequent period, when mean L of sugar-beet and of theleafiest wild beet type was 2.5, there was an inverse relationbetween E and L of the three wild types, and E of sugar-beetwas then much greater than that of the wild type with equalL but was little different from that of the wild type with smallestL (about 1.5). It is concluded that the development of sugar-beetfrom its wild ancestors by selection and breeding has not affectedthe intrinsic photosynthetic efficiency of the leaves, but hasdiminished the effect of mutual-interference between leaves,so that E falls less rapidly as L increases, i.e. it has decreasedthe leaf-density dependence of E. This change may be relatedto the difference in form between sugar-beet and wild beet plants.     

Net CO(2) Assimilation Rate of Grapevine Leaves in Response to Trunk Girdling and Gibberellic Acid Application

Net CO₂ assimilation rate (A), stomatal conductance (g_s), and weight per unit leaf area (W) were determined on Thompson Seedless grapevines grown in the field. Treatments included fruit set applications of gibberellic acid (40 milligrams gibberellic acid (GA₃) per liter) to vines, shoots and clusters, alone and in combination with trunk girdling. Leaf A and g_s were measured prior to and 3, 6, and 13 days after fruit set. Weight per unit leaf area was determined on leaves collected subsequent to gas exchange measurements. Leaf A of girdled vines was reduced approximately 30% when compared to the control 13 days after treatment. The reduction in A due to girdling was not as great when vines were sprayed with GA₃. GA₃ sprays alone had no significant effect on A. Stomatal conductance was reduced by girdling 13 days after treatment. Weight per unit leaf area was 17% greater for trunk girdled vines when compared to the controls. Results indicate GA₃ affected net CO₂ assimilation rate only on girdled vines, a treatment which increased weight per unit leaf area.     

Maintenance and Constructive Respiration, Photosynthesis, and Net Assimilation Rate in Seedlings of Pitch Pine (Pinus rigida Mill.)

Pitch pine seedlings were grown at constant temperature andphotoperiod. Net CO₂-uptake h^–1 g^–1 leaves decreasedsteadily during ontogeny until leaf production ceased. Thereafter,there was no change or a slight increase. Though the ontogeneticpattern was the same in populations native to different geographicareas, there were differences among populations in the rateof CO₂-uptake. Root respiration, calculated from the differencebetween CO₂-uptake and net assimilation rate, accounted for6 to 69 per cent of diurnal assimilation. Growth of shoots and roots was episodic and out of phase. Spurtsof growth could be forecast by high rates of respiration 4 weeksearlier, probably because high-energy syntheses precede theprocesses of cell elongation and cell wall formation. Maintenanceand constructive respiration were substantially higher for theshoots (85 per cent leaf tissue) than for the roots. Constructiverespiration was proportional to photosynthesis.     

High Net Assimilation Rates of Sunflower Plants in an Arid Climate

Net assimilation rates of sunflower plants (Heliantkus annuus),grown widely spaced with soil nutrients and water non-limiting,reached 2.0 g dm^–3 wk^–1 in clear weather at midsummerin an arid climate. These rates exceed all previously recordedand are roughly double those hitherto taken to be maximal insunflower. They suggest that maximum rates of photosysnthesisin the most active leaves were 50–65 mg CO₂ dm_–2h_–1. These high rates are a response to the high levels of radiationin the arid climate. They imply that (given non-limiting soil)plants can attain higher productivity in the arid climate thanin any other.     

Effect of Rubisco Activase Deficiency on the Temperature Response of CO2 Assimilation Rate and Rubisco Activation State: Insights from Transgenic Tobacco with Reduced Amounts of Rubisco Activase

The activation of Rubisco in vivo requires the presence of the regulatory protein Rubisco activase. To elucidate its role in maintaining CO₂ assimilation rate at high temperature, we examined the temperature response of CO₂ assimilation rate at 380 μL L⁻¹ CO₂ concentration (A₃₈₀) and Rubisco activation state in wild-type and transgenic tobacco (Nicotiana tabacum) with reduced Rubisco activase content grown at either 20°C or 30°C. Analyses of gas exchange and chlorophyll fluorescence showed that in the wild type, A₃₈₀ was limited by ribulose 1,5-bisphosphate regeneration at lower temperatures, whereas at higher temperatures, A₃₈₀ was limited by ribulose 1,5-bisphosphate carboxylation irrespective of growth temperatures. Growth temperature induced modest differences in Rubisco activation state that declined with measuring temperature, from mean values of 76% at 15°C to 63% at 40°C in wild-type plants. At measuring temperatures of 25°C and below, an 80% reduction in Rubisco activase content was required before Rubisco activation state was decreased. Above 35°C, Rubisco activation state decreased slightly with more modest decreases in Rubisco activase content, but the extent of the reductions in Rubisco activation state were small, such that a 55% reduction in Rubisco activase content did not alter the temperature sensitivity of Rubisco activation and had no effect on in vivo catalytic turnover rates of Rubisco. There was a strong correlation between Rubisco activase content and Rubisco activation state once Rubisco activase content was less that 20% of wild type at all measuring temperatures. We conclude that reduction in Rubisco activase content does not lead to an increase in the temperature sensitivity of Rubisco activation state in tobacco.The catalytic sites of Rubisco must be activated for CO₂ fixation to take place. This requires the carbamylation of a Lys residue at the catalytic sites to allow the binding of Mg²⁺ and ribulose 1,5-bisphosphate (RuBP; Andrews and Lorimer, 1987). Rubisco activase facilitates carbamylation and the maintenance of Rubisco activity by removing inhibitors such as tight-binding sugar phosphates from Rubisco catalytic sites in an ATP-dependent manner (Andrews, 1996; Spreitzer and Salvucci, 2002; Portis, 2003; Parry et al., 2008). The activity of Rubisco activase is regulated by the ATP/ADP ratio and redox state in the chloroplast (Zhang and Portis, 1999; Zhang et al., 2002; Portis, 2003).In many plant species, Rubisco activation state decreases at high temperature in vivo (Crafts-Brandner and Salvucci, 2000; Salvucci and Crafts-Brandner, 2004b; Cen and Sage, 2005; Yamori et al., 2006b; Makino and Sage, 2007). However, it is unclear what the primary mechanisms underlying the inhibition of Rubisco activation are and whether Rubisco deactivation limits CO₂ assimilation rate at high temperature. It has been proposed that Rubisco activation state decreases at high temperature, because the activity of Rubisco activase is insufficient to keep pace with the faster rates of Rubisco inactivation at high temperatures (Crafts-Brandner and Salvucci, 2000; Salvucci and Crafts-Brandner, 2004a, 2004c; Kim and Portis, 2006). In in vitro assays using purified Rubisco and Rubisco activase, the activity of Rubisco activase was sufficient for the activation of Rubisco at the optimum temperature but not at high temperatures (Crafts-Brandner and Salvucci, 2000; Salvucci and Crafts-Brandner, 2004a, 2004c). ATP hydrolysis activity of Rubisco activase in vitro has varying temperature optima among species (e.g. 25°C in Antarctic hairgrass [Deschampsia antarctica] and spinach [Spinacia oleracea] but 35°C in tobacco [Nicotiana tabacum] and cotton [Gossypium hirsutum]), and Rubisco activase more readily dissociates into inactive forms at high temperature, causing a loss of Rubisco activase capacity (Crafts-Brandner and Law, 2000; Salvucci and Crafts-Brandner, 2004b). Moreover, the rates of inhibitor formation by misprotonation of RuBP during catalysis increased at higher temperatures (Salvucci and Crafts-Brandner, 2004c; Kim and Portis, 2006). CO₂ assimilation rates and plant growth were improved under heat stress in transgenic Arabidopsis expressing thermotolerant Rubisco activase isoforms generated by either gene-shuffling technology (Kurek et al., 2007) or chimeric Rubisco activase constructs (Kumar et al., 2009). These results support the view that the reduction of Rubisco activase activity limits the Rubisco activation and, therefore, the CO₂ assimilation rates at high temperatures.It has also been suggested that the decrease in CO₂ assimilation rate at high temperatures is caused by a limitation of RuBP regeneration capacity (e.g. electron transport capacity) rather than by Rubisco deactivation per se (Schrader et al., 2004; Wise et al., 2004; Cen and Sage, 2005; Makino and Sage, 2007; Kubien and Sage, 2008). These groups suggest that Rubisco deactivation at high temperature may be a regulatory response to the limitation of one of the processes contributing to electron transport capacities. For example, at high temperature, protons can leak through the thylakoid membrane, impairing the coupling of ATP synthesis to electron transport (Pastenes and Horton, 1996; Bukhov et al., 1999, 2000). As the electron transport capacity becomes limiting, ATP/ADP ratios and the redox potential of the chloroplast decline, causing a loss of Rubisco activase activity and, in turn, a reduction in the Rubisco activation state (Zhang and Portis, 1999; Zhang et al., 2002; Sage and Kubien, 2007). Based on this understanding, the decline in the Rubisco activation state at high temperature may be a regulated response to a limitation in electron transport capacity rather than a consequence of a direct effect of heat on the integrity of Rubisco activase.Temperature dependence of CO₂ assimilation rate shows a considerable variation with growth temperature (Berry and Björkman, 1980; Hikosaka et al., 2006; Sage and Kubien, 2007). Plants grown at low temperature generally exhibit higher CO₂ assimilation rates at low temperatures compared with plants grown at high temperature, but they exhibit lower rates at high temperature. Furthermore, both the temperature response of Rubisco activation state and the limiting step of CO₂ assimilation rate (a Rubisco versus RuBP regeneration limitation) have been shown to differ depending on growth temperature (Hikosaka et al., 1999; Onoda et al., 2005; Yamori et al., 2005, 2006a, 2006b, 2008). This suggests that the regulation of Rubisco activation state could also differ in plants grown at different growth temperatures. Here, we analyzed the effects of Rubisco activase content on Rubisco activation state and CO₂ assimilation rate at leaf temperatures ranging from 15°C to 40°C in tobacco grown under two different temperature regimes (day/night temperatures of 20°C/15°C or 30°C/25°C). We used wild-type and transgenic tobacco with a range of reductions in Rubisco activase content to examine the dependence of Rubisco activation on Rubisco activase content over the range of leaf temperatures (Mate et al., 1993, 1996).     

Effect of High Temperature on Photosynthesis in Beans (II. CO2 Assimilation and Metabolite Contents)

The effect of high temperatures on CO2 assimilation, metabolite content, and capacity for reducing power production in non-photorespiratory conditions has been assessed in two different bean (Phaseolus vulgarus L.) varieties, Blue Lake (commercially available in the United Kingdom) and Barbucho (a noncommercially bred Chilean variety), which are known to differ in their resistance to extreme high temperatures. Barbucho maintains its photosynthetic functions for a longer period of time under extreme heat compared with Blue Lake. The CO2 assimilation rate was increased by increases in temperature, with a decrease in ratio of rates of temperatures differing by 10[deg]C. It is suggested that limitations to CO2 assimilation are caused by metabolic restrictions that can be differentiated between those occurring in the range of 20 to 30[deg]C and 30 to 35[deg]C. It is likely that changes in the capacity for Calvin cycle regeneration and starch synthesis affect photosynthesis in the range of 20 to 30[deg]C. But following an increase in temperature from 30 to 35[deg]C, the supply of reducing power becomes limiting. From analysis of adenylate concentration, transthylakoid energization, and, indirectly, NADPH/NADP+ ratio, it was concluded that the limitation in the assimilatory power was due to an oxidation of the NADPH/NADP+ pool. In the range of 30 to 35[deg]C, the photosystem I quantum yield increased and photosystem II maintained its value. We conclude that the reorganization of thylakoids observed at 30 to 35[deg]C increased the excitation of photosystem I, inducing an increase in cyclic electron transport and a decrease in the supply of NADPH, limiting carbon assimilation.     

The Effect of Rapid Temperature Increase on the Growth Rate of Wheat Leaves

The growth rate of the first leaf of eight-day-old wheat plants was measured using a DLT-2 highly sensitive linear displacement transducer. Leaf extensibility was evaluated from the growth rate under the increase in the pulling force by 2 g. An increase in the air temperature resulted in the doubling of the transpiration rate and immediate slowing of the leaf growth followed by the leaf shrinkage. However, growth was later resumed almost completely. Heat treatment did not induce any changes in the leaf extensibility, indicating that cell-wall mechanical properties were not changed. Growth retardation was supposed to result from a decrease in the water content in the leaf tissues because the balance between water influx from roots and its loss through transpiration was shifted toward the water loss. An initial drop in the relative water content (RWC) indicates such a misbalance. Subsequent growth resumption coincided with a decreased water deficiency. Since the rate of transpiration was not reduced, RWC and growth rate restoring evidently occurred due to the activated water uptake by roots, which can be explained by the increased hydraulic permeability detected in our experiments.