Carbon Assimilation at Low Carbon Dioxide Levels: II. THE PROCESSES OF APPARENT ASSIMILATION

The relation of the net uptake or output of carbon dioxide bydetached leaves of Pelargonium zonale or wheat to ambient carbondioxide concentration was investigated at two or three lightintensities. The statistics of fitted curves were used as datain analysis of variance. For Pelargonium the results were consistentwith a hypothesis of a ‘straight balance’ betweena rate of photosynthetic uptake proportional to concentrationand a constant rate of respiratory production. For wheat, however,the curve was steeper near than at lower carbon dioxide levels;this disproved the ‘straight balance’ hypothesisand was consistent with an increase in carbon dioxide fixationor a reduction in output over a limited concentration rangeon either side of . The characteristics of light respiration, possibly carbon dioxidedependent, were investigated further in an experiment on theeffect of oxygen concentrationupon r values for two species(P. zonale and Hydrangea sp.) at two light intensities; theywere also studied by measuring the ‘burst’ of carbondioxide output when leaves were darkened after illuminationat four different light intensities and at two temperatures. was linearly related to oxygen tension up to 610 mm partialpressure of mercury and a fivefold increase in light intensityhad only a very small effect indicating that photoxidation wasnot important. The carbon dioxide burst on darkening showedrelations to temperature and previous light intensity quitedifferent from those of which should be proportional to lightrespiration. These results, therefore, do not support the viewthat the burst represents the persistence of an enhanced lightrespiration.     

In-Phase Cycling of Photosynthesis and Conductance at Saturating Carbon Dioxide Pressure Induced by Increases in Water Vapour Pressure Deficit

Bunce, J. A. 1987. In-phase cycling of photosynthesis and conductanceat saturating carbon dioxide pressure induced by increases inwater vapour pressure deficit.—J. exp. Bot. 38: 1413–1420. The leaf to air water vapour deficit was increased suddenlyfrom about 1·0 to 2·5 IcPa for single leaves ofsoybean (Glycine max L. Merr.) plants held at 30 °C, 2·0mmol m ^–2 s^–1 photosynthetic photon flux density(PPFD) and carbon dioxide pressures saturating to photosynthesis.After a lag of about 10 min, photosynthetic rate and stomatalconductance to water vapour began to decrease, and then cycledin phase with each other. The period of the cydes was about20 min. During these cycles the substomatal carbon dioxide pressurewas constant in the majority of leaves examined, and was alwaysabove saturation for photosynthesis. Epidermal impressions showedthat most stomata changed in aperture during the cycles, andthat very few were ever fully closed. Water potential measuredon excised discs changed by at most 0·1 MPa from theminima to the maxima in transpiration rate. In contrast, forleaves of sunflower (Helianthus animus L.) grown at low PPFD,the increase in VPD led to leaf wilting and decreased photosynthesis,followed by recovery of turgor and photosynthesis as stomatalconductance began to decrease. In these leaves photosynthesisand conductance then cycled approximately 180° out of phase.It is suggested that in soybeans decreased leaf conductanceinduced by high VPD provided a signal which decreased the rateof photosynthesis at carbon dioxide saturation by a mechanismthat was not related to a water deficit in the mesophyll. Key words: Photosynthesis, stomatal conductance, cycling, vapour pressure deficit     

Studies in Stomatal Behaviour: V. THE ROLE OF CARBON DIOXIDE IN THE LIGHT RESPONSE OF STOMATA

It was found that stomata on illuminated leaves, both of Pelargoniumand wheat, opened much wider where the leaf surface was enclosedin a small volume of air, as in a normal porometer cup, thanelsewhere. This was shown for both species by the infiltrationmethod, and for Pelargonium by Lloyd's method and direct microscopicalobservation also. The effect was shown not to be due to pressure of the porometercup or glass plate on the leaf, or to temperature differences,nor directly to the lack of movement or high humidity of theenclosed air. A considerable body of data was collected which appeared tosupport the hypothesis that the wide opening was due to accumulationof some volatile substance produced by the leaf, but all theresults were also consistent with the view that it was causedby reduction in the carbon dioxide content of the enclosed airbelow the normal 0·03 per cent. owing to photosynthesis.Further crucial experiments with both the porometer and infiltrationmethods left virtually no doubt that the latter hypothesis wascorrect. This extreme sensitivity of stomata to carbon dioxide concentrationwithin the range 0·03 per cent. to zero is discussedin relation to their operation in nature, and a possible biologicaladvantage is suggested. The bearing of the effect upon porometer investigations is alsodiscussed and it is concluded that for all quantitative or semi-quantitativeexperimentation it is essential to use a cup detached betweenreadings, or at least swept with air such as surrounds the restof the leaf, and to have the upper leaf surface above the cuparea freely exposed or similarly swept. For qualitative investigationof the light response of stomata the traditional form of cupmay be used. The importance is stressed of allowing porometer readings toreach equilibrium under one set of conditions before changingto another, when investigating the ‘closing’ or‘opening’ effects of external factors. Several subsidiary effects, observed in the course of the investigation,are discussed; in particular an effect of humidity upon therate of response to other factors.     

The Measurement of Stomatal Responses to Stimuli in Leaves and Leaf Discs

A comparison has been made of stomatal responses in intact leaves,leaf discs supplied with water via their cut edges and leafdiscs floating on water. Xanthium pennsylvanicum leaf discswatered via their cut edges appeared to be more turgid thanintact leaves; this considerably slowed down the rate of stomatalopening but it slightly increased the final steady-state stomatalopening. When the water potential of such leaf discs was loweredby pre-treatment with mannitol solutions rates of stomatal openingincreased whereas maximum steady-state openings decreased. In tobacco leaf discs floating on water the stomata in contactwith water were wider open than those in contact with normalair and they did not respond to treatment with carbon dioxide-freeair. The rate of photosynthesis was severely reduced in tobaccoleaf discs floating with the lower epidermis on water, mostprobably owing to the slow rate of diffusion of carbon dioxidein water. By floating such discs on osmotica the degree of stomatalopening was increased, however, a response to treatment withcarbon dioxide-free air was still not measurable. It is postulatedthat, on account of the relative unavailability of carbon dioxidefrom the water, the carbon dioxide concentration in the substomatalcavities of the lower surface is abnormally low, irrespectiveof whether ordinary air or carbon dioxide-free air is availableto the upper surface. A comparison between porometer readings and measurements ofsiliconerubber impressions of stomatal pores taken from insidethe porometer cup confirmed that the silicone-rubber impressionmethod of assessing stomatal responses to stimuli has severelimitations, especially at small stomatal apertures.     

The Effect of Grain Number per Ear (Sink Size) on Source Activity and its Water-Relations in Wheat

Blum, A., Mayer, J. and Golan, G. 1988. The effect of grainnumber per ear (sink size) on source activity and its water-relationsin wheat.–J. exp. Bot. 39: 106–114. Work was done to evaluate the nature of sink-source relationshipsin wheat (Triticum aestivum L.), when the strength of the sinkwas modified by the removal of half of the grain from the earat about anthesis. The main hypothesis was that sink-sourcerelationship would be modified by water stress and that a weakersink would improve the drought resistance of the source. Two experiments were performed. The first experiment evaluatedthe effect of de-graining in two wheat varieties grown in thefield. The second experiment (in the greenhouse) evaluated theeffect of de-graining in plants subjected to water stress afteranthesis by immersing the root system in a solution of polyethyleneglycol (6000), as compared with non-stressed controls. In bothexperiments measurements were performed after de-graining toprovide data on leaf gas exchange, leaf water potential, osmoticadjustment of leaves and ears (greenhouse), the percent of stemweight loss as an index of stem reserve mobilization, finalroot weight (greenhouse) and ear weight components. De-graining caused a decrease in flag leaf stomatal conductance,carbon exchange rate (CER) and transpiration and an increasein flag leaf water potential. These effects were stronger withwater stress. De-graining did not affect osmotic adjustmentin the flag leaf but induced better adjustment in glumes andawns. De-graining decreased the percent of stem weight lossand increased final root weight, especially under drought stress. A weaker sink was, therefore, considered to improve plant droughtresistance in terms of the maintenance of higher leaf waterpotential, a larger root, a better osmotic adjustment in theear and, possibly, increased flag leaf longevity. The ‘cost’of this improved drought resistance was in reduced flag leafCER and reduced stem (and root?) reserve mobilization. Key words: Drought resistance, carbon exchange rate, stomata, transpiration, osmotic adjustment, leaf water potential, root, awns, yield     

Experimental Studies of the Factors Controlling Transpiration: II. THE RELATION BETWEEN TRANSPIRATION RATE AND LEAF WATER CONTENT

Data are presented which show, when stomatal control is eliminated,that wheat leaves may lose 5–6 per cent. and Pelargoniumleaves 10–12 per cent. of their water without any reductionin the transpiration rate. Experiments in which Pelargonium and wheat leaves, with stomatalcontrol present, were submitted to cycles of changing watercontent also failed to establish any direct relation betweentranspiration rate and leaf water content. It is concluded that leaf water content over the range of 70–100per cent. of that present in the turgid state has no significanteffect in determining the rate of water loss from leaves. A repetition of Knight's experiment showed that stomata openedin still air and closed in moving air. This was not recordedby Knight, who used a porometer cup permanently attached tothe leaf. It is concluded that the higher transpiration raterecorded by Knight after a period of still air was due to widerstomatal aperture and not to the higher leaf water content assuggested by him.     

The Influence of NO-3 and NH+4 Nutrition on the Gas Exchange Characteristics of the Roots of Wheat (Triticum aestivum) and Maize (Zea mays) Plants

Respiratory oxygen consumption by roots was 1·4- and1·6-fold larger in NH⁺₄-fed than in NO^-₃-fed wheat (Triticumaestivum L.) and maize (Zea mays L.) plants respectively. Higherroot oxygen consumption in NH⁺₄-fed plants than in NO^-₃-fedplants was associated with higher total nitrogen contents inNH⁺4-fed plants. Root oxygen consumption was, however, not correlatedwith growth rates or shoot:root ratios. Carbon dioxide releasewas 1·4- and 1·2-fold larger in NO⁺3-fed thanin NH⁺₄-fed wheat and maize plants respectively. Differencesin oxygen and carbon dioxide gas exchange rates resulted inthe gas exchange quotients of NH^-₄-fed plants (wheat, 0·5;maize, 0·6) being greatly reduced compared with thoseof NO^-₃-fed plants (wheat, 1·0; maize, 1·1). Measuredrates of HCO^-₃ assimilation by PEPc in roots were considerablylarger in 4 mM NH⁺₄-fed than in 4 NO^-₃ plants (wheat, 2·6-fold;maize, 8·3-fold). These differences were, however, insufficientto account for the observed differences in root carbon dioxideflux and it is probable that HCO^-₃ uptake is also importantin determining carbon dioxide fluxes. Thus reduced root extension in NH⁺₄-fed compared with NO^-₃-fedwheat plants could not be ascribed to differences in carbondioxide losses from roots.Copyright 1993, 1999 Academic Press Triticum aestivum, wheat, Zea mays, maize assimilation, ammonium assimilation, root respiration     

The Interactive Effects of Atmospheric Carbon Dioxide and Light on Stem Elongation in Seedlings of Four Species

Four species,Sinapis albaL.,Medicago sativaL.,Gypsophila paniculataL.andPicea abies(L.) Karsten, were grown in three light regimes:darkness, low light (25 µmol m^-2s^-1for 10 min d^-1) andhigh light (120 µmol m^-2s^-1for 12 h  d^-1) and fourlevels of carbon dioxide: 0, 350, 700 and 1400±50 µll^-1. Germination was not affected by any of the treatments.The effects of carbon dioxide on stem elongation were identicalin low and high light: stem length increased at a decreasingrate with level of carbon dioxide in all species. Level of carbondioxide also affected stem elongation in complete darkness,but the pattern was more complex and varied among species. Totalweight did not vary with level of carbon dioxide to any significantextent in either darkness or low light, but increased with levelof carbon dioxide at high light in all four species. Due tothe absence of any effect of carbon dioxide on growth in darknessand low light, we suggest the effects of carbon dioxide on stemelongation are independent of effects on growth and may be dueto a direct interaction with developmental processes. In contrast,level of carbon dioxide had little effect on allocation patternsin the dark and low light experiments, but had marked effectsin high light. Therefore, the effect of carbon dioxide on allocationwas probably due to the effects of carbon dioxide on growthrather than to any direct interaction between carbon dioxideand development. An understanding of the mechanisms by whichcarbon dioxide affects development may help us understand theoften variable effects of carbon dioxide upon plants.Copyright1998 Annals of Botany Company Sinapis albaL.;Medicago sativaL.;Gypsophila paniculataL. andPicea abies(L.) Karsten; elevated carbon dioxide; stem elongation; germination; allocation; phytochrome.     

Studies in Stomatal Behaviour: VI. AN INVESTIGATION OF THE LIGHT RESPONSES OF WHEAT STOMATA WITH THE ATTEMPTED ELIMINATION OF CONTROL BY THE MESOPHYLL

As in the previous investigation (Part I), stomatal responsesin wheat were followed by means of porometer readings; betweenthese, air was forced through the stomata to sweep out the substomatalcavities. Instead of forcing the whole of a relatively slowair-flow in through the stomata, however, a fast flow was sweptacross the leaf surface and a portion of this passed into theintercellular space system. This helped to maintain the desiredcarbon dioxide content close to the stomatal openings and thestomata could thus be treated with different carbon dioxideconcentrations. A factorial experiment was carried out in which6 carbon dioxide concentrations from zero to 0084 per cent,were combined with 3 light intensities from 90 to 800 f.c, the18 treatments being replicated 6 times in three ‘66 latinsquares’. A supplementary experiment in which the same6 carbon dioxide treatments were given in darkness was carriedout in duplicate. The results confirmed previous findings inthat the stomata showed no appreciable response to variationof external carbon dioxide supply between zero and 001 percent, concentration and that a large and highly significantlight response was found at each of these two carbon dioxidelevels. This is held to indicate the existence of a light effect(direct or indirect) not operating by reduction of the internalcarbon dioxide content of the guard cells. On the assumptionthat the rates of air flow through the stomata were adequate,the combined results of the two experiments are interpretedmainly in terms of two direct effects of light upon the stomata,one depending on photosynthetic reduction of carbon dioxidein the guard cells and the other, mentioned above, not so operating.To these must be added the indirect effect responsible for the‘transmission’ described in Part 1, which mightpossibly account for the whole of the second direct effect postulated.Finally, if the rates of flow were in fact grossly inadequate,the trends attributed to the first direct effect mentioned abovemight have been due to indirect control by the mesophyll viathe intercellular space atmosphere. Such control must accountfor part of the light responses which occur under natural conditions.The natural light response is thus made up of at least two andmore probably four components—two direct and two indirect,in each case one operating by the internal carbon dioxide andthe other not. A highly significant diurnal rhythm of stomatalmovement under constant illumination and temperature is shownto occur in wheat. The measure of stomatal resistance used (logresistance per 10,000 stomata) is discussed, and it is concludedthat although it is empirical a much more satisfactory measureis not at present available.     

Injury to Rice Plants Caused by Complete Submergence; A Contribution by Ethylerie (Ethene)

Complete submergence of rice plants (Oryza sativa L. cv. ‘IR42’)in dilute nutrient solution for 3–6 d almost stopped theaccumulation of dry matter, depressed soluble carbohydrate concentrationby over 75% and promoted chlorosis in fully expanded leaves.Increase in fresh weight by the shoots was not impaired. Extensionby the youngest visible leaf was stimulated. Extension by thenext leaf to appear was retarded by submergence. These growthresponses to submergence were associated with a 1-5-fold increasein the partial pressure of endogenous ethylene (ethene). Applying ethylene (0.3–0.35 Pa) in the gas-phase to non-submergedplants reproduced some, but not all, of these effects of submergence.Thus, greater leaf extension and chlorosis of submerged plantscould be attributable to accumulated ethylene but neither theslow relative growth rate nor the decreased extension of leavesemerging after the start of submergence could be so attributed. Two cultivars (‘FR13A’ and ‘Kurkaruppan’)already known to tolerate submergence, differed little fromsubmergence-intolerant ‘IR42’ in their relativegrowth rate and soluble carbohydrate concentration during submergence.However, their underwater leaf extension was less than in ‘IR42’and chlorosis was much less prevalent, especially in ‘FR13A’.Similarly, ethylene supplied to non-submerged plants was a lesseffective promotor of leaf extension and chlorosis in the twosubmergence tolerant cultivars. Application of 1.0 kPa carbondioxide in the gas-phase prevented the chlorosis response toethylene. The results indicate that accumulated ethylene is a likely causeof fast leaf extension and chlorosis in submergence intolerantforms of rice, particularly when amounts of dissolved carbondioxide are minimal. Key words: Oryza sativa L., aeration, ethylene (ethene), stress-tolerance     

Control of the Acclimation of Photosynthesis to Light and Temperature in Relation to Partitioning of Photosynthate in Developing Soybean Leaves

Photosynthetic acclimation was examined by exposing third trifoliolateleaves of soybeans to air temperatures of 20 to 30°C andphotosynthetic photon flux densities (PPFD) of 150 to 950µmolphotons m^–2 s^–1 for the last 3 d before they reachedmaximum area. In some cases the environment of the third leafwas controlled separately from that of the rest of the plant.Photosynthesis, respiration and dry mass accumulation were determinedunder the treatment conditions, and photosynthetic capacity,and dry mass and protein content were determined at full expansion.Photosynthetic capacity, the light-saturated rate of net carbondioxide exchange at 25°C and 34 Pa external partial pressureof carbon dioxide, could be modified between 21 and 35 µmolCO₂ m^–2 s^–1 by environmental changes after leaveshad become exporters of photosynthate. Protein per unit leafmass did not differ between treatments, and photosynthetic capacityincreased with leaf mass per unit area. Photosynthetic capacityof third leaves was affected by the PPFD incident on those leaves,but not by the PPFD on other leaves on the plant. Photosyntheticcapacity of third leaves was affected by the temperature ofthe rest of the plant, but not by the temperature of the thirdleaves. Photosynthetic capacity was linearly related to carbondioxide exchange rate in the growth regimes, but not to daytimePPFD. At high PPFD, and at 25 and 30°C, mass accumulationwas about 28% of the mass of photosynthate produced. At lowerPPFD, and at 20°C, larger percentages of the photosynthateproduced accumulated as dry mass. The results suggest that photosynthatesupply is an important factor controlling leaf structural growthand, consequently, photosynthetic acclimation to light and temperature. Key words: Glycine max (L.) Merr., photosynthesis, temperature acclimation, light acclimation, photosynthate partitioning     

The Effects of Cytokinins and ABA on Stomatal Behaviour of Maize and Commelina

Epidermal strips and leaf fragments of Commelina and leaf fragmentsof maize were incubated on solutions containing naturally-occurringor synthetic cytokinins and/or ABA. The effects of these treatmentson stomatal behaviour were assessed. Cytokinins alone did notpromote stomatal opening in either species but concentrationsof both zeatin and kinetin from 10^–3 to 10^–1 molm^–3 caused some reversal of ABA-stimulated closure ofmaize stomata. The reversal of the ABA effect increased withincreasing cytokinin concentration. Cytokinins had no effecton ABA-stimulated closure of Commelina stomata. When appliedalone, at high concentration (10^–1 mol m^–3), toCommelina epidermis or leaf pieces both zeatin and kinetin restrictedstomatal opening. Key words: ABA, Cytokinins, Stomata, Maize, Commelina     

The Effect of Sodium on Growth of Water-stressed Sugar beet

Sugar beet grown in solution culture, with or without a supplementof 16 millequivalents per litre of sodium, were subjected towater stress with polyethylene glycol solutions of –0.4,–3, and –8 bar osmotic potential. With the –0.4bar solution leaf water potential was between –6 and –8bar and leaf relative water content about 90 per cent. Decreasingthe solution osmotic potential to –8 bar decreased leafwater potential to about –15 bar and relative water contentto 75 per cent; leaves stopped expanding and transpiration andcarbon dioxide uptake were decreased by 80 and 50 per cent respectively.Net assimilation rates were only slightly decreased becauseleaf growth was decreased more than carbon dioxide assimilation.Relative growth rates of the plants were decreased by 8 percent at –3 bar and by 15 per cent at –8 bar. Sodium absorbed by the plant accumulated mainly in the leavesand petioles; it increased the water content of the leaves andstorage root and the plant fresh weight. Sodium decreased theleaf osmotic potential, slightly increased leaf water potential,and significantly increased turgor. It had no effect on carbondioxide uptake, transpiration, net assimilation rate, or relativegrowth rate. Sodium increased the rate at which the leaf areagrew and it is concluded that it did so by altering the leafwater balance.     

Studies in Stomatal Behaviour: V. THE ROLE OF CARBON DIOXIDE IN THE LIGHT RESPONSE OF STOMATA

Experiments are described in which the responses of wheat stomatato carbon dioxide concentration (0·00, 0·01, 0·02,0·03 per cent.), light intensity (275, 625, 975 f.c.),and rate of air flow (2, 5, 12·5 l./hr.) were studied. Reduction of carbon dioxide concentration from 0·03 to0·01 per cent. resulted in marked stomatal opening; furtherreduction to 0·00 per cent, was accompanied by a slightbut not significant closure. These effects were found at alllight intensities and rates of flow, except at 975 f.c. with2 l./hr. air flow, where no effect of carbon dioxide concentrationwas detected. This last is attributed to excessive depletionof the carbon dioxide supply by assimilation. The apparent lowerlimit of 0·01 per cent, carbon dioxide causing maximalstomatal opening is discussed in relation to recent assimilationexperiments. Increase of light intensity caused considerable stomatal opening,this effect being as great with air of 0·00 and 0·01per cent. as with higher concentrations of carbon dioxide. Thissuggests an effect of light on stomatal movement other thanthat exerted indirectly through photosynthesis by the mesophylcells. Increased rate of flow of dry air caused closure of the stomata;this was shown to be a drying effect and was absent when moistair was used.     

Stomatal Control of Water Loss in Siratro (Macroptilium atropurpureum (DC) Urb.), a Tropical Pasture Legume

Stomatal conductance of siratro declined linearly as leaf waterpotential fell until zero conductance was reached at –10bar. In a grass/legume pasture stomata of siratro respondedto humidity (saturation deficit), and to a lesser extent toleaf water potential, such that leaf water potential did notfall below –9 bar, whereas that of the grass continuedto decline for most of the day. The dual response of siratroto both humidity and leaf water potential suggests that thisspecies has an efficient two-stage stomatal control of waterloss which provides an explanation of its higher leaf waterpotential and greater drought avoidance compared with sown grassesin semi-arid areas of north-eastern Australia. Macroptilium atropurpureum (DC) Urb., siratro, Desmodium uncinatum, stomatal control, stomatal conductance, water loss, leaf water potential, drought avoidance, saturation deficit     

The Anisotropy of the Mesophyll and CO2 Capture Sites in Vicia faba L. Leaves at Low Light Intensities

Experiments are reported on the spatial distributions of isotopiccarbon within the mesophyll of detached leaves of the C₃ plantVicia faba L. fed ¹⁴CO₂ at different light intensities. Eachleaf was isolated in a cuvette and ten artificial stomata providedspatial continuity between the ambient atmosphere (0.03–0.05%v/v CO₂) and the mesophyll from the abaxial leaf side. Paradermalleaf layers exhibited spatial profiles of radioactivity whichvaried with the intensity of incident light in 2 min exposures.At low light, when biochemical kinetics should limit CO₂ uptake,sections through palisade cells contained most radioactivity.As the light intensity was increased to approximately 20% offull sunlight, peak radioactivity was observed in the spongycells near the geometric mid-plane of the mesophyll. The resultsindicate that diffusion of carbon dioxide within the mesophyllregulated the relative photosynthetic activity of the palisadeand spongy cells at incident photosynthetically active lightintensities as little as 110 µE m^–2 s^–1 whenCO₂ entered only through the lower leaf surface. Key words: CO₂ capture sites, Vicia faba L., Artificial stomata     

Carbon Dioxide Production in Early Anaerobiosis

1. Slices of swede tissue placed under nitrogen produce carbondioxide and ethanol in equal amounts after an initial phaselasting about 1.5 hours. During this initial phase some 2 µM./g.fr. wt. of extra carbon dioxide is produced. The productionof such extra carbon dioxide is not affected by iodoacetate,fluoride, or arsenite which inhibit glycolysis or by dinitrophenolwhich stimulates glycolysis. Slices incubated in air in thepresence of cyanide also produce extra carbon dioxide. 2. A second extra burst of carbon dioxide can be induced aftersome hours of anaerobiosis by treating slices with methyleneblue, DPN, or TPN, or as a result of a short air experience. 3. Experiments with labelled sugars support the view that theextra carbon dioxide originates ultimately from carbohydrate,being released, it is proposed, in the oxidative decarboxylationof either pyruvate or 6-phosphogluconate. Carbon dioxide productionthen continues so long as oxidants are available in the cell,finally coming to a standstill when cell components reach theirreduced states.     

Effect of Elevated CO2 on Stomatal Size and Distribution in Perennial Ryegrass

Plants of ryegrass (Lolium perenne L. cv. Melle) were grownfrom the early seedling stage in growth cabinets at a day/nighttemperature of 20/15 °C, with a 12-h photoperiod, and aCO₂ concentration of either 340 or 680 ± 15 µl1^–1 CO₂. Young, fully-expanded, acclimated leaves fromprimary branches were sampled for length of stomata, and ofepidermal cells between stomata, numbers of stomata and epidermalcells per unit length of stomatal row, numbers of stomatal rowsacross the leaf and numbers of stomatal rows between adjacentvein ridges. Elevated CO₂ had no significant effect on any ofthe measured parameters. Elevated CO₂, Lolium perenne, ryegrass, stomatal distribution, stomatal size     

Further Effects of Light Intensity, Carbon Dioxide Concentration, and Day Temperature on the Growth of Chrysanthemum morifolium cv. Bright Golden Anne in Controlled Environments

In earlier work the effects of light intensity over the range31 to 250 J cm^–2 day^–1 and carbon dioxide concentrationfrom 325 to 900 ppm with 8-h days at 18.3 °C and 16-h nightsat 15.6 °C were described. The present paper is concernedwith three further experiments with light levels up to 375 Jcm^–2 day^–1 (which corresponds to the daily totalin a glasshouse in southern England in early May or August andthe intensity is approximately that of mid-winter sunshine),carbon dioxide concentration up to 1500 ppm, and day temperaturesof 18.3 to 29.4 °C. Final plant weight was increased by light over the range 125–375J cm^–2 day^–1 and by carbon dioxide over the range325–900 ppm, with positive interaction between them; thisinteraction was increased by raising the temperature to 23.9°C and somewhat more at 29.4 °C day temperature. Leaf-arearatio and specific leaf area were reduced by increasing eitherlight or carbon dioxide but there was little effect of temperature.Leaf-weight ratios were uniform within experiments but therewere small consistent differences between one experiment andthe other two which also affected leaf-area ratios. Mean unit leaf rate was scarcely affected by day temperatureover the range investigated. There were the usual increasesdue to increased light and carbon dioxide concentration anda consistent difference in absolute value between one experimentand the other two. These differences in mean unit leaf rateare illustrated in detail in the ontogenetic trend of unit leafrate and plant size. Lower unit leaf rates were to a considerableextent compensated for by increased leaf-area ratios in theusual way. Despite the substantial differences in day temperature the specificwater contents (g water g dry weight^–1) differed little,showing in the majority of cases higher values in the highertemperature for otherwise similar treatment combinations. Flower development was somewhat delayed at 23.9 °C day temperature,and substantially so at 29.4 °C. Lateral branch length wasincreased at 23.9 °C and excessively so at 29.4 °C.This reveals quite clearly that a temperature optimum for vegetativegrowth may not be the optimum for flowering performance norproduce a desirable plant shape. Despite the marked effects of temperature on rate of flowerdevelopment, the relationship between flower development andthe ratio of flower to total weight was the same for all treatmentcombinations in all three experiments and coincident with thatreported earlier. Gasometric determinations indicated that respiratory loss bythe whole plant was a smaller proportion of net photosyntheticgain at a temperature of 29.4 °C than at 18.3 °C andwas likewise a smaller proportion at 1500 ppm carbon dioxidethan at 325 ppm. If photorespiration of leaves is assumed tobe as great as their dark respiration, the respiratory lossesare in the range of 31–50 per cent of the gross gain.Greater rates of photorespiration would increase the proportionaterespiratory loss.     

Stomatal Control of Photosynthesis of Eucalyptus globulus Labill. Trees under Field Conditions in Portugal

Pereira, J. S., Tenhunen, J. D. and Lange, O. L. 1987. Stomatalcontrol of photosynthesis of Eucalyptus globulus Labill. treesunder field conditions in Portugal.—J. exp. Bot. 38: 1678–1688. Stomatal behaviour of adult leaves of Eucalyptus globulus treeswas studied under field conditions in Portugal. In the absenceof severe plant water stress stomata were open when the summedtotal of photosynthetically active photon flux density incidenton both leaf surfaces was above 100 µmol m²s¹ and leafconductance to water vapour reached 245 mmol m ² s¹ on a total(both epidermes) leaf area basis. The stomata of both leaf epidermesresponded similarly to changes in solar radiation and waterstress. Water stress resulted in decreasing daily maxima inleaf conductance as predawn leaf water potential decreased.Maximal leaf conductance decreased to less than 50 mmol m ²s ¹ when predawn leaf water potential decreased below —1·0MPa. At similar values of predawn leaf water potential stomatawere more closed as the leaf to air water vapour partial pressuredifference increased. The effect of increasing air dryness onstomata was greatest at high predawn leaf water potential. Dailymaxima in photosynthetic rates and in leaf conductance werelinearly related to one another in spring and summer. Both decreasedwith increase in leaf water stress. In autumn and winter, increasesin leaf conductance occurring under natural conditions duringthe course of the day were not necessarily accompanied by increasesin net photosynthesis. Stomata were more closed in the afternoonthan in the morning at the same rates of net photosynthesis,temperature or leaf to air water vapour partial pressure difference. Key words: Eucalyptus globulus,, photosynthesis, stomata, water stress.