The Occurrence of Endogenous Rhythms in the Coleoptiles in Various Cereal Genera

The rate of growth of the coleoptiles was determined from photographstaken by infra-red radiation. CO₂ output was measured by meansof an infra-red gas analyser. The rhythm of CO₂ output from the coleoptile of Avena was inducedby a change from red light to darkness. It has a period of about24 hours and agrees in timing with the growth-rate rhythm previouslyrecorded. Some degree of rhythmicity in the growth-rate was found in Triticumvulgare (var. ‘Eclipse’) and in Secale cereale (var.Petkus). Very slight indications of rhythmicity were found inTriticum spelta and in Hordeum vulgare. Negative results wereobtained with Oryza sativa and with Zea mays. Where rhythmicityin the coleoptile is less strongly developed, the peaks comecloser together, the interval being about 18–20 hours.Cereals cannot be sharply separated into two groups accordingto the presence or absence of rhythmicity in the coleoptile.Of the genera examined, the most marked endogenous rhythms occurin Avena. It is doubtful if the ability of the coleoptile toexhibit an endogenous rhythm has any beneficial effect on thedevelopment of the seedling. Under normal conditions of germinationinduction of the rhythm would not occur.     

STUDIES ON THE RE-ASSIMILATION OF RESPIRATORY CO2 IN ILLUMINATED LEAVES

Experiments were performed, using rice, barley and Hydrangealeaves, to examine the re-assimilation of respiratory ¹⁴CO₂while photosynthesis is going on in an open air flow system. It was found that the leaves which had assimilated ¹⁴CO₂ beforehandevolved, when kept under photosynthesizing conditions, threeto four tenths (variable according to plant species and externalconditions) of the amount of ¹⁴CO₂ to be produced in the dark.Such an incomplete re-utilization of ¹⁴CO₂ was observed alsoin spinach leaf homogenate as well as in the leaves which hadpreviously absorbed ¹⁴C-glucose. The ¹⁴CO₂ output in rice leaves was found to be acceleratedby the light of high intensity. A possibility of light stimulationon the respiration was suggested. (Received October 7, 1961; )     

Effect of Phosphlnothricin (Glufosinate) on Photosynthesis and Chlorophyll Fluorescence Emission by Barley Leaves Illuminated Under Photorespiratory and Non-Photorespiratory Conditions

The effect of phosphinothricin (PPT), an inhibitor of glutaminesynthetase, on several aspects of photosynthesis has been studiedin primary leaves of barley (Hordeum vulgare L.). When photorespirationwas suppressed, either by increasing CO₂ concentration to 0.7%,or by decreasing O₂ concentration to 1%, feeding the illuminatedleaves with 0·5 or 1·0 mM PPT did not affect photosynthesisto a noticeable extent. Conversely, when PPT-fed leaves wereilluminated in air, CO₂ uptake decreased continuously. Modificationof the components of chlorophyll fluorescence quenching indicatedincreased reduction of Q_A, the primary acceptor of photosystemII, and increased chloroplast energization. Feeding of PPT toleaves illuminated in air increased the quantum requirementof photosynthesis and decreased photosynthetic rate of oxygenevolution in saturating [CO₂] and high light intensity. It isconcluded that the effect of PPT on the photochemical processesis indirect, through the inhibition of CO₂ assimilation probablycaused by the depletion of intermediates of the reductive pentosephosphate cycle. Key words: Feeding, Hordeumvulgare L., quenching coefficients     

Antagonism Between Malate and Ethylene in the Regulation of Avena sativa Coleoptile Elongation

Etiolated Avena sativa L. coleoptile sections were used to determinethe influence of C₂H₄ on in vivo and in vitro rates of CO₂ fixation,and to measure the influence of various permutations of C₂H₄,CO₂, and malate on growth. Whereas 1 mM malate or 320 µI^-1 CO₂ stimulated growth by approximately 100 per cent, inhibitionof growth by 10-8 µ I_-1 C₂H₄ was substantial only in thepresence of malate or CO₂ The increase in growth rate in responseto these two agents was eliminated by the simultaneous applicationof C₂H₄. The in vivo rate of dark [¹⁴C]bicarbonate fixationand in vitro enzymic assays of fixation were not measurablyinhibited by C₂H₄. These results are discussed in the lightof evidence which indicates that CO₂-stimulated growth is mediatedby dark fixation. The data do not support the view that C₂H₄inhibition of growth results from an inhibition of fixation,but suggests that C₂H₄ may inhibit some step in the processby which malate stimulates growth.     

Leaf Characteristics and Net Gas Exchange of Diploid and Autotetraploid Citrus

The effect of tetraploidy on leaf characteristics and net gasexchange was studied in diploid (2x ) and autotetraploid (4x) ‘Valencia’ sweet orange (Citrus sinensis (L.)Osb.) and ‘Femminello’ lemon (Citrus limon (L.)Burm. f.) leaves. Comparisons between ploidy levels were madeunder high irradiance (I) in a growth chamber or low total Iin a glasshouse. Tetraploids of both species had thicker leaves,larger mesophyll cell volume and lower light transmittance thandiploids regardless of growth I. Mesophyll surface area perunit leaf area of 2x leaves was 5–15% greater than on4x leaves. Leaf thickness and mesophyll cell volume were greaterin high I leaves than low I leaves. In high I, average leafarea was similar for 2x and 4x leaves, whereas in low I it was30% greater in 4x than in 2x leaves. Nitrogen and chlorophyllconcentration per cell increased with ploidy level in both growthconditions. The ratio of chlorophyll a:b was 25% greater in2x than in 4x leaves. When net CO₂assimilation rate (A_CO2) wasbased on leaf area, 4x orange leaves had 24–35% lowerA_CO2than their diploids. There were no significant differencesin A_CO2between 2x and 4x orange or lemon leaves when expressedon a per cell basis. Overall, lower A_CO2per unit leaf area oftetraploids was related to increase in leaf thickness, largermesophyll cell volume, the decrease in mesophyll area exposedto internal air spaces, and the lower ratio between cell surfaceto cell volume. Such changes probably increased the resistanceto CO₂diffusion to the site of carboyxlation in the chloroplasts. Cell volume; chlorophyll; irradiance; leaf thickness; nitrogen; photosynthesis; ploidy; Citrus limon ; C. sinensis ; ‘Valencia’ sweet orange; ‘Femminello’ lemon     

Acid Metabolism and Respiration in Succulent Compositae: III. Further Experiments with Kleinia radicans Haw

Evidence has been obtained that starving leaves of Kleinia radicansin the summer condition produce a volatile substance, whichreacts with potassium permanganate, and which accumulates andpoisons the leaves when they are enclosed, as in a Dixon respirometer.A microrespirometer has been designed for use with continuousair-currents. Using this, the course of oxygen intake by leavesin darkness resembles that of CO₂ output (previous results)and shows an initial phase of diurnal fluctuation of O₂ intake.Humidity has also some effect, for an early increase in O₂ intakeoccurs under dry conditions.     

Photosynthetic Carbon Reduction and Carbon Oxidation Cycles are the Main Electron Sinks for Photosystem II Activity During a Mild Drought

Stomatal closure can explain the inhibition of net CO₂ uptakeby a leaf subjected to a mild drought: the photosynthetic apparatusappears resistant to lack of water. Changes in both the watercontent of leaves maintained in a constant environment and theambient CO₂ molar fraction during measurements on well-hydratedleaves lead to similar effects on net CO₂ uptake and whole chainelectron transport as estimated by leaf chlorophyll fluorescencemeasurements. In particular, it is shown that photosystem II(PSII) functioning and its regulation are not qualitativelychanged during desiccation and that the variations in PSII photochemistrycan simply be understood by changes in substrate availabilityin this condition. Moreover, an analysis of the literature showsthat when inhibition of net CO₂ uptake by C₃ leaves under drought(Phaseolus vulgaris L., Helianthus annus L. and Solanum tuberosumL.) was lower than 80 %, elevated CO₂ completely restored thephotosynthetic capacity. The CO₂ molar fraction in the chloroplastsdeclines as stomata close in drying leaves. As a consequence,in C₃ plants, ribulose-1,5-bisphosphate oxygenation increasesand becomes the main sink for photosynthetic electrons. Dependingon the prevailing photon flux density, the O₂ uptake throughphotorespiratory activity can entirely replace carbon dioxideas an electron acceptor, or not. The rate of the Mehler reactionremains low and unchanged during desiccation. However, droughtcould also involve CO₂-sensitive modification of the photosyntheticmetabolism depending on plant growth conditions and possiblyalso on plant species.     

Effect of Elevated CO2 on the Photosynthesis, Respiration and Growth of Perennial Ryegrass

Single, seed-grown plants of ryegrass (Lolium perenne L. cv.Melle) were grown for 49 d from the early seedling stage ingrowth cabinets at a day/night temperature of 20/15 C, witha 12 h photoperiod, and a CO₂ concentration of either 340 or680µI 1^–1 CO₂. Following complete acclimation tothe environmental regimes, leaf and whole plant CO₂ effluxesand influxes were measured using infra-red gas analysis techniques.Elevated CO₂ increased rates of photosynthesis of young, fullyexpanded leaves by 35–46% and of whole plants by morethan 50%. For both leaves and whole plants acclimation to 680µI^–1 CO₂ reduced rates of photosynthesis in bothCO₂ regimes, compared with plants acclimated to 340µll^–1. There was no significant effect of CO₂ regime onrespiration rates of either leaves or whole plants, althoughleaves developed in elevated CO₂ exhibited generally lower ratesthan those developed in 340µI I^–1 CO₂. Initially the seedling plants in elevated CO₂ grew faster thantheir counterparts in 340µI I^–1 CO₂, but this effectquickly petered out and final plant weights differed by onlyc. 10%. Since the total area of expanded and unexpanded laminaewas unaffected by CO₂ regime, specific leaf area was persistently13–40% lower in elevated CO₂ while, similarly, root/shootratio was also reduced throughout the experiment. Elevated CO₂reduced tissue nitrogen contents of expanded leaves, but hadno effect on the nitrogen contents of unexpanded leaves, sheathsor roots. The lack of a pronounced effect of elevated CO₂ on plant growthwas primarily due to the fact that CO₂ concentration did notinfluence tiller (branch) numbers. In the absence of an effecton tiller numbers, any possible weight increment was restrictedto the c. 2.5 leaves of each tiller. The reason for the lackof an effect on tillering is not known. Key words: Lolium perenne, ryegrass, elevated CO₂, photosynthesis, respiration, growth, development     

Stomatal Density and Index of Fossil Plants Track Atmospheric Carbon Dioxide in the Palaeozoic

It has been demonstrated that the leaves of a range of foresttree species have responded to the rising concentration of atmosphericCO₂ over the last 200 years by a decrease in both stomatal densityand stomatal index. This response has also been demonstratedexperimentally by growing plants under elevated CO₂ concentrations.Investigation of Quaternary fossil leaves has shown a correspondingstomatal response to changing CO₂ concentrations through a glacial-interglacialcycle, as revealed by ice core data. Tertiary leaves show asimilar pattern of stomatal density change, using palynologicalevidence of palaeo-temperature as a proxy measure of CO₂ concentration.The present work extends this approach into the Palaeozoic fossilplant record. The stomatal density and index of Early Devonian,Carboniferous and Early Permian plants has been investigated,to test for any relationship that they may show with the changesin atmospheric CO₂ concentration, derived from physical evidence,over that period. Observed changes in the stomatal data givesupport to the suggestion from physical evidence, that atmosphericCO₂ concentrations fell from an Early Devonian high of 10-12times its present value, to one comparable to that of the presentday by the end of the Carboniferous. These results suggest thatstomatal density of fossil leaves has potential value for assessingchanges in atmospheric CO₂ concentration through geologicaltime.Copyright 1995, 1999 Academic Press Aglaophyton major, Sawdonia ornata, Swillingtonia denticulata, Lebachia frondosa, Juncus effusus, Psilotum nudum, Araucaria heterophylla, stomatal density, stomatal index, Palaeozoic CO₂     

The Damping and Reinitiation of the Circadian Rhythm of CO2 Output in Bryophyllum Leaves in Relation to their Malate Content

The circadian rhythm of CO₂ output in leaves of Bryophyllumfedtschenkoi damps out after 3–4 d in continuous darknessand a CO₂-free air stream at 15°C. The rhythm is reinitiatedafter a single exposure to white light of 2, 4, 6 or 8 h duration,damps out again after a further 3–4 d and can be reinitiatedfor a second time by a further exposure to light. During the exposure to light there is a burst of CO₂ outputconsistent with the decarboxylation of malate, and the rhythmbegins afterwards with an initial high rate of CO₂ fixation.Malate gradually accumulates in the leaves in continuous darknessto attain a maximum value (35 mol m^–3) at the time whenthe circadian rhythm disappears, and decreases to a low value(19 mol m^–3) after a 4 h exposure to light which reinitiatesrhythmicity. These results support the hypothesis that damping of the rhythmof CO₂ output in continuous darkness is due to the accumulationof malate in the leaf cells, eventually reaching such a levelthat its removal from the cytoplasm into the vacuole cannottake place, with the result that PEPc activity, upon which therhythm of CO₂ output depends, remains allosterically inhibited. Key words: CAM, circadian rhythm, Bryophyllum, CO₂-fixation, malate metabolism     

Simultaneous CO2- and 16O2/18O2-gas exchange and fluorescence measurements indicate differences in light energy dissipation between the wild type and the phytochrome-deficient aurea mutant of tomato during water stress

The CO₂-, H₂O- and ¹⁶O₂/¹⁸O₂ isotopic-gas exchange and the fluorescencequenching by attached leaves of the wild-type and of the phytochrome-deficienttomato aurea mutant was compared in relation to water stressand the photon fluence rate. The chlorophyll content of aurealeaves was reduced and the ultra-structure of the chloroplastswas altered. Nevertheless, the maximum rate of net CO₂ uptakein air by the yellow-green leaves of the aurea mutant was similarto that by the dark-green wild-type leaves. However, less O₂was produced by the leaves of the aurea mutant than by leavesof the wild-type. This result indicates a reduced rate of photosyntheticelectron flux in aurea mutant leaves. No difference in bothphotochemical and non-photochemical fluorescence quenching wasfound between wild-type and aurea mutant leaves. Water stresswas correlated with a reversible decrease in the rates of bothnet CO₂ uptake and transpiration by wild-type and aurea mutantleaves. The rate of gross ¹⁶O₂ evolution by both wild-type andaurea mutant leaves was fairly unaffected by water stress. Thisresult shows that in both wild-type and aurea leaves, the photochemicalprocesses are highly resistant to water stress. The rate ofgross ¹⁸O₂ uptake by wild-type leaves increased during waterstress when the photon fluence rate was high. Under the sameconditions, the rate of gross ¹⁸O₂ uptake by ^aurea mutant leavesremained unchanged. The physiological significane of this differencewith respect to the (presumed) importance of oxygen reductionin photoprotection is discussed. Key words: Water stress, gas exchange, fluorescence quenching, Lycopersicon esculentum, mutant (tomato, aurea), energy dissipation     

Comparison of Palaeobotanical Observations with Experimental Data on the Leaf Anatomy of Durmast Oak [Quercus petraea(Fagaceae)] in Response to Environmental Change

To test whether stomatal density measurements on oak leaf remainsare reliable tools for assessing palaeoatmospheric carbon dioxideconcentration [CO₂], under changing Late Miocene palaeoenvironmentalconditions, young seedings of oak (Quercus petraea,Liebl.) weregrown at elevatedvs.ambient atmospheric [CO₂] and at high humiditycombined with an increased air temperature. The leaf anatomyof the young oaks was compared with that of fossil leaves ofthe same species. In the experiments, stomatal density and stomatalindex were significantly decreased at elevated [CO₂] in comparisonto ambient [CO₂]. Elevated [CO₂] induced leaf cell expansionand reduced the intercellular air space by 35%. Leaf cell sizeor length were also stimulated at high air humidity and temperature.Regardless of a temperate or subtropical palaeoclimate, leafcell size in fossil oak was not enhanced, since neither epidermalcell density nor length of the stomatal apparatus changed. Theabsence of these effects may be attributed to the phenologicalresponse of trees to climatic changes that balanced temporalchanges in environmental variables to maintain leaf growth underoptimal and stable conditions.Quercus petraea,which evolvedunder recurring depletions in the palaeoatmospheric [CO₂], maypossess sufficient phenotypic plasticity to alter stomatal frequencyin hypostomatous leaves allowing high maximum stomatal conductanceand high assimilation rates during these phases of low [CO₂].Copyright1998 Annals of Botany Company Atmospheric CO₂, high humidity, elevated temperature,Quercus petraea,durmast oak, Late Miocene, palaeoclimates, leaf anatomy, stomatal density, stomatal index     

Effects of elevated CO2 concentrations on three montane grass species: III. Source leaf metabolism and whole plant carbon partitioning

Agrostis capillaris L.⁵, Festuca vivipara L. and Poaalpina L.were grown in outdoor open-top chambers at either ambient (340 3µmol mol^–1) or elevated (6804µmol mol^–1)concentrations of atmospheric carbon dioxide (CO₂) for periodsfrom 79–189 d. Photosynthetic capacity of source leaves of plants grown atboth ambient and elevated CO₂ concentrations was measured atsaturating light and 5% CO₂. Dark respiration of leaves wasmeasured using a liquid phase oxygen electrode with the buffersolution in equilibrium with air (21% O₂, 0.034% CO₂). Photo-syntheticcapacity of P. alpina was reduced by growth at 680 µmolmol^–1 CO₂ by 105 d, and that of F. vivipara was reducedat 65 d and 189 d after CO₂ enrichment began, suggesting down-regulationor acclimation. Dark respiration of successive leaf blades ofall three species was unaltered by growth at 680 relative to340 µmol mol^–1 CO₂. In F. vivipara, leaf respirationrate was markedly lower at 189 d than at either 0 d or 65 d,irrespective of growth CO₂ concentration. There was a significantlylower total non-structural carbohydrate (TNC) concentrationin the leaf blades and leaf sheaths of A. capillaris grown at680µmol mol^–1 CO₂. TNC of roots of A. capillariswas unaltered by CO₂ treatment. TNC concentration was increasedin both leaves and sheaths of P. alpina and F. vivipara after105 d and 65 d growth, respectively. A 4-fold increase in thewater-soluble fraction (fructan) in P. alpina and in all carbohydratefractions in F. vivipara accounted for the increased TNC content. In F. vivipara the relationship between leaf photosyn-theticcapacity and leaf carbohydrate concentration was such that therewas a strong positive correlation between photosynthetic capacityand total leaf N concentration (expressed on a per unit structuraldry weight basis), and total nitrogen concentration of successivemature leaves reduced with time. Multiple regression of leafphotosynthetic capacity upon leaf nitrogen and carbohydrateconcentrations further confirmed that leaf photosynthetic capacitywas mainly determined by leaf N concentration. In P. alpina,leaf photosynthetic capacity was mainly determined by leaf CHOconcentration. Thus there is evidence for down-regulation ofphotosynthetic capacity in P. alpina resulting from increasedcarbohydrate accumulation in source leaves. Leaf dark respiration and total N concentration were positivelycorrelated in P. alpina and F. vivipara. Leaf dark respirationand soluble carbohydrate concentration of source leaves werepositively correlated in A. capillaris. Changes in source leafphotosynthetic capacity and carbohydrate concentration of plantsgrown at ambient or elevated CO₂ are discussed in relation toplant growth, nutrient relations and availability of sinks forcarbon. Key words: Elevated CO₂, Climate change, grasses, carbohydrate partitioning, photosynthesis, respiration     

CO2 fixation in leaves of a CAM plant without lower epidermis and the effect of CO2 on their deacidification

The effects of peeling the epidermis off Bryophyllum daigremontianumleaves on CO₂ uptake in light and darkness were investigated.Light-induced CO₂ uptake in the daytime was markedly enhancedin the peeled leaves, but dark fixation of CO₂ carried out atmidnight was not. The difference in promotion of CO₂ uptakein light and darkness was due to stomatal closing in the dayand opening at night. Also, deacidification was strikingly inhibitedby CO₂ in peeled leaves. (Received February 3, 1977; )     

Protein synthesis in Xanthium leaf development

Young, expanding Xanthium leaves had many soluble proteins;older leaves had progressively fewer. The leaves that grew themost rapidly incorporated the most ¹⁴CO₂ into their proteins.The relative intensity of ¹⁴CO₂ incorporation into the differentsoluble proteins changed with leaf development. (Received November 17, 1969; )     

Elevated carbon dioxide affects the patterning of subsidiary cells in Tradescantia stomatal complexes

The influence of elevated CO₂ concentration (670 ppm) on thestructure, distribution, and patterning of stomata in Tradescantialeaves was studied by making comparisons with plants grown atambient CO₂. Extra subsidiary cells, beyond the normal complementof four per stoma, were associated with nearly half the stomatalcomplexes on leaves grown in elevated CO₂. The extra cells sharedcharacteristics, such as pigmentation and expansion, with thetypical subsidiary cells. The position and shape of the extrasubsidiary cells in face view differed in the green and purplevarieties of Tradescantia. Substomatal cavities of complexeswith extra subsidiary cells appeared larger than those foundin control leaves. Stomatal frequency expressed on the basisof leaf area did not differ from the control. Stomatal frequencybased on cell counts (stomatal index) was greater in leavesgrown in CO₂-enriched air when all subsidiary cells were countedas part of the stomatal complex. This difference was eliminatedwhen subsidiary cells were included in the count of epidermalcells, thereby evaluating the frequency of guard cell pairs.The extra subsidiary cells were, therefore, recruited from theepidermal cell population during development. Stomatal frequencyin plants grown at elevated temperature (29 C) was not significantlydifferent from that of the control (24 C). The linear aggregationsof stomata were similar in plants grown in ambient and elevatedCO₂. Since enriched CO₂ had no effect on the structure or patterningof guard cells, but resulted in the formation of additionalsubsidiary cells, it is likely that separate and independentevents pattern the two cell types. Plants grown at enrichedCO₂ levels had significantly greater internode lengths, butleaf area and the time interval between the appearance of successiveleaves were similar to that of control plants. Porometric measurementsrevealed that stomatal conductance of plants grown under elevatedCO₂ was lower than that of control leaves and those grown atelevated temperature. Tradescantia was capable of regulatingstomatal conductance in response to elevated CO₂ without changingthe relative number of stomata present on the leaf. Key words: Elevated CO₂, stomata, subsidiary cells, patterning     

The Influence of Prior Water Stress and Abscisic Acid Foliar Spraying on Stomatal Responses to CO2, IAA, ABA, and Calcium in Leaves of Solanum melongena

The influence of a water stress or foliar ABA spraying pretreatmenton stomatal responses to water loss, exogenous ABA, IAA, Ca²⁺,and CO₂ were studied using excised leaves of Solanum melongena.Both pretreatments increased stomatal sensitivity of water loss,in the presence and absence of CO₂, but decreased stomatal sensitivityto exogenous ABA. CO₂ greatly reduced the effect of exogenouslyapplied ABA. IAA decreased leaf diffusion resistance for controland ABA sprayed leaves, but did not influence the LDR of previouslywater-stressed leaves. CA²⁺ did not influence LDR of any leavesof any treatments. Key words: Water stress, stomatal response, pretreatments     

Metabolism of Barley Leaves Inoculated with Erysiphe graminis Merat

Inoculating Proctor barley leaves with Erysiphe graminis decreasedrates of photosynthesis, after an initial lag period, and increasedrespiration. Increasing the area inoculated progressively decreased ratesof photosynthesis, but the effects cannot be attributed to asimple loss of leaf area. When less than 30 per cent of a leafwas inoculated, decreases were equivalent to area losses greaterthan those inoculated; when more than 30 per cent was inoculatedthe photo-synthetic losses were equivalent to area losses lessthan those inoculated. Although the relative effects of E. graminis on photosynthesisand respiration were of the same order, the absolute effectson photosynthesis were greater than those on respiration. Inoculating30 per cent of a leaf decreased photosynthesis by 5–6mg CO₂/dm²/hr from 12.9 in the uninoculated controls to 7.3.Respiration increased by 0.6 mg CO₂/dm/hr, from 1.7 to 2.3-     

Stomatal Density Responses of Egyptian Olea europaea L. Leaves to CO2 Change Since 1327 BC

We have attempted to separate the effects of CO₂ and temperaturechange on stomatal density by examining ancient leaf materialof Olea europaea L. The distribution of this species is confinedto a Mediterranean type climate, so that O. europaea leavesof different ages will have formed under similar temperaturesbut different CO₂ levels over the last 3000 years. Stomataldensity measurements have been made upon leaves of O. europaeaoriginating from King Tutankhamun's tomb dating from 1327 BC,and have been compared with values obtained from Egyptian O.europaea material dating from pre-332 BC, 1818 and 1978 AD.Together, the four dates provide a record of how the plant hasresponded to increases in atmospheric CO₂ concentration duringthat time. The results demonstrate that in accordance with similarstudies examining the stomatal density response of plants overthree time scales (hundreds, thousands and tens of thousandsof years) stomatal density falls as CO₂ levels increase. Sincewe have examined a natural system with leaves developing undersimilar environmental temperatures the results confirm observationsfrom experimental studies in which plants were grown under thesame temperature but different CO₂ regimes.Copyright 1993, 1999Academic Press Olea europaea, stomatal density, atmospheric CO₂, temperature, climate change     

Ethylene Release from Leaves of Xanthium strumarium L. and Zea mays L.

The release of ethylene into sealed Erlenmeyer flasks by intactleaves and leaf discs of Xanthium strumarium L. a C₃ plant andZea mays L. a C₄ plant were compared both in white light andin darkness. The effects of the presence or absence of addedCO₂ (in the form of sodium bicarbonate) the photosynthetic inhibitor3-[3,4-dichlorophenyl]-l, l-dimethyl urea (DCMU) and 1-aminocyclopropane-1-carboxylicacid (ACC), the precursor of ethylene in higher plants, werealso investigated. The rate of ethylene release from leaf tissue of Xanthium inthe absence of added CO₂ was markedly reduced in the light (i.e.at the CO₂ compensation point). Treatments that would enhancethe CO₂ availability to the tissue (i.e. added bicarbonate,darkness, treatment with DCMU) allowed higher levels of ethylenerelease. Incubation of the tissue with ACC considerably enhancedthe release of ethylene compared to that from the correspondingcontrol tissue without ACC. However, the pattern of ethylenerelease induced by the various treatments was similar with orwithout added ACC. When tissue, in the absence of added CO₂, was transferred fromlight to darkness, and back to light for 90 min periods, theethylene release rates Increased during the interposed darkperiod but resumed the lower rate during the final light period.The addition of CO₂ in the light resulted in a similar rateof ethylene release to that found in the dark. The overall pattern of ethylene release from Zea leaf tissuesubjected to light and dark in the presence or absence of addedCO₂ was similar to that of Xanthium. However, two or three timesmore ethylene was released from maize leaves in the light whenCO² was added compared to that generated in the dark. This isin marked contrast to Xanthium, where, under the light conditionsused, the ethylene release rate in the dark equalled or exceededthat occurring in the light, even in the presence of high levelsof CO₂. A very low rate of ethylene release was observed atthe CO₂ compensation point of maize. A speculative model is presented to explain how photosyntheticactivity might act as a key factor in regulating ethylene evolutionfrom leaf tissue in these experiments. It invokes the conceptof an inhibition by CO₂ of ethylene retention or breakdown thuspermitting more ethylene to be released from the leaves.