Measuring the Canopy Net Photosynthesis of Glasshouse Crops

A null balance method is described for measuring net photosynthesisof mature canopies of cucumber and other protected crops overperiods of 10 min in a single-span glasshouse (c. 9m x 18m inarea). Accuracy of control of the CO₂ concentration in the greenhouseatmosphere is within ±10 vpm of the normal ambient level(c. 350 vpm). The amounts of CO₂ used in canopy net photosynthesisare measured with linear mass flowmeters accurate to within±0.80g. The total errors incurred in measuring canopynet photosynthesis at an ambient CO₂ level are estimated tobe of the order of ± 1·2% in bright light (350W m^–2, PAR)and ±3·6% in dull light (100W m^–2, PAR). Measurements of the rates of net photosynthesis of a maturecanopy of a cucumber crop were made at near-ambient CO₂ concentrationsover a range (0–350 W m^–2) of natural light fluxdensities. A model of light absorption and photosynthesis applicableto row crops was used to obtain a net photosynthesis versuslight response curve for the cucumber crop. At a light fluxdensity of 350 W m^–2 the fitted value of canopy net photosynthesiswas 2.65 mg CO₂ m^–2s^–1 (equivalent to over 95 kgCO₂ ha^–1h^–1). The results are discussed in relationto the need for CO₂ supplements to avoid depletion in both ventilatedand unventilated glasshouses during late spring and summer. Key words: Glasshouse crops, cucumber, measurement, canopy photosynthesis, light, CO₂     

Light Interception and Photosynthetic Efficiency in Some Glasshouse Crops

Productivity of glasshouse crops is strongly limited by lightreceipt, and efficient interception and use of light in photosynthesisis correspondingly important. Mature row crop canopies of cucumberand tomato intercepted about 76% of the light incident on theirupper surfaces; about 18% was lost through gaps between therows. Light transmitted through the entire depth of the canopywas reflected back by white plastic on the ground, so that thelower surface of the canopy received approximately 13% of thelight incident on the upper surface. The light flux incidenton the sides of these canopies (c. 2m tall and 6m x 16m in area)amounted to some 20–30% of that incident on the uppersurface. About 32% of daylight falling on the glasshouse (c.9m x 18m in area) was intercepted by the glasshouse structureand glazing; of the 68% entering the house, some fell on headlandsoccupying 35% of the glasshouse area. The loss of light to headlands,and the gain from canopy side-lighting, would be relativelysmaller for larger glasshouses. At near-ambient CO₂ concentrations, net photosynthetic ratesof the cucumber canopy were comparable to those of closed canopiesof other glasshouse and field crops which have maximum lightconversion efficiencies of 5–8µg CO₂ J^–1 at50–200 W m^–2 incident light flux density. Efficiencydecreases only slightly with stronger light. Glasshouse cropswith CO₂ enrichment to 1200 vpm achieve conversion efficienciesof 7–10µg CO₂ J^–1. Efficiencies of utilizationof intercepted light, on an energy basis, reach 6–10%in various field and glasshouse crops with near-ambient CO₂,and reached an exceptional 11% for the cucumber canopy. Glasshousecrops with CO₂ enrichment achieve maximum efficiency of lightenergy utilization between 12% and 13%. Key words: Glasshouse cucumber and tomato, light interception and utilization, photosynthetic efficiency, row crops     

Photosynthesis of Stands of Tomato, Cucumber and Sweet Pepper Measured in Greenhouses under Various CO2-concentrations

The rate of net photosynthesis (P) of whole plant stands oftomato (Lycopersicon esculentum Mill.), cucumber (Cucumis sativusL.) and sweet pepper (Capsicum annuum L.) was measured in sixlong-term experiments in large greenhouses under normal operatingconditions and CO₂-concentrations between 200 and 1200 µmolmol^-1. The objective was to quantify the responses to lightand carbon dioxide and to obtain data sets for testing simulationmodels. The method of measuring canopy photosynthesis involvedan accurate estimation of the greenhouse CO₂ balance, usingnitrous oxide (N₂O) as tracer gas to determine, on-line, theexchange rate between greenhouse and outside air. The estimatedrelative error in the observed P was about ± 10%, exceptthat higher relative errors could occur under particular conditions. A regression equation relating P to the photosynthetically activeradiation, the CO₂ concentration and the leaf area index explained83-91% of the variance. The main canopy photosynthesis characteristicscalculated with the fitted regression equations were: canopyP_max 5-9 g m^-2 h^-1 CO₂ uptake; ratio P_max/LAI 1·5-3 gm^-2 h^-1; light compensation point 32-86 µmol s^-1 m^-2;light use efficiency (quantum yield) at low light 0·06-0·10µmol µmol^-1 and CO₂ compensation point 18-54 µmolmol^-1. The results were related to the prevailing conditions.Copyright1994, 1999 Academic Press Canopy photosynthesis, Capsicum annuum L., carbon dioxide, CO₂, CO₂ balance, CO₂ use efficiency, cucumber, _{Cucumis sativus} L., glasshouse, greenhouse, light use efficiency, Lycopersicon esculentum Mill., sweet pepper, tomato, tracer gas     

Canopy Photosynthesis of Tomato, Cucumber and Sweet Pepper in Greenhouses: Measurements Compared to Models

Two models for canopy photosynthesis (modified versions of thoseof Acock et al. , 1978 and of Thornley, 1976) were examinedby comparison with experimental photosynthesis data of cucumber(Cucumis sativus L.), sweet pepper (Capsicum annuum L.) andtomato (Lycopersicon esculentum Mill.). The data were obtainedin six large-scale, long-term, semi-commercial cultivationsin greenhouses (Nederhoff and Vegter, 1994). Measured environmentalconditions and measured LAI were input to the model. The emphasiswas on the models' sensitivity to the prevailing CO₂ concentration. The (modified) Acock model with 'standard' (originally published)parameters underestimated the photosynthesis rate. This modeltuned to one of our experimental data sets did not fit verywell to the other data sets. As expected, if the model was tunedto each particular data set, it was fairly in agreement withthe measurements, but the fitted parameter values were sometimesquestionable. With the (modified) Thornley model it was obligatoryto estimate or tune the light extinction. The model performedreasonably if all parameters were tuned and also if only thelight extinction was tuned. The modified models were considered usable for practical applications,after parameter tuning. As the sensitivity to CO₂ was not alwaysequal among the models and the measurements, care should betaken when applying the models for CO₂ supply control.Copyright1994, 1999 Academic Press Canopy photosynthesis, Capsicum annuum L., carbon dioxide, cucumber, CO₂, Cucumis sativus L., glasshouse, greenhouse, Lycopersicon esculentum Mill., measurements, model, sweet pepper, tomato     

Factors Controlling Induction of External Carbonic Anhydrase and Change in K?(CO2) of Photosynthesis in Chlorella regularis

Transfer of algal cells of Chlorella regularis from 3% CO₂ inair into ordinary air in the light increased external carbonicanhydrase (CA) activity as well as photosynthetic affinity forCO₂ by several-fold within 2 h. Since no noticeable differencewas observed in CA activity between intact cells and cell homogenates,CA seemed to be mainly localized on the cell surface. Changesin CA activity and K_?(CO₂) of photosynthesis were not observedin the dark. CA induction was 50%-inhibited by incubation with10 µM DCMU during adaptation of high-CO₂ cells to air,whereas it was considerably suppressed when high-CO₂ cells preincubatedwith DCMU in the light for 6 h or without DCMU in the dark for24 h were used. The change in K_?(CO₂) of photosynthesis wasonly slightly affected by DCMU. Uncoupler like carbonylcyanide-m-chlorophenyl-hydrazone(CCCP) and inhibitors of mitochondrial respiration (KCN plussalicylhydroxamic acid) suppressed CA induction during adaptationof high-CO₂ cells to low CO₂ conditions. These results suggest that photosynthesis is not essential forCA induction in Chlorella regularis when some amounts of photosyntheticproducts are previously stored in the cells and respirationis active. A decrease in K_?(CO₂) of photosynthesis during adaptationfrom high to low CO₂ was mostly independent on photosynthesis.However, light is essential for both phenomena. (Received July 16, 1990; Accepted January 21, 1991)     

Dry Matter Production in a Tomato Crop: Measurements and Simulation

Simulation of dry matter production by the explanatory glasshousecrop growth model SUKAM (Gijzen, 1992, Simulation Monographs),based on SUCROS87 (Spitters, Van Keulen and Van Kraalingen,1989, Simulation and systems management in crop protection),was validated for tomato. In the model, assimilation rates arecalculated separately for shaded and sunlit leaf area at differentcumulative leaf area in the canopy, taking into account thedifferent interception of direct and diffuse components of light.Daily crop gross assimilation rate (P_gd) is computed by integrationof these rates over total crop leaf area and over the day. Leafphotochemical efficiency and potential gross assimilation rateat saturating light depend on temperature and CO₂ concentrationand are approximated as being identical in the whole canopy.Crop growth results from P_gd minus maintenance respiration rate(R_m; dependent on temperature and crop dry weight), multipliedby the conversion efficiency (carbohydrates to structural drymatter; C_f). Growth experiments (periodic destructive harvest) with differentplanting dates and plant densities and two data-sets from commerciallygrown crops, were used for model validation. Hourly averagesfor global radiation outside the glasshouse, glasshouse temperatureand CO₂ concentration, together with measured leaf area index,dry matter distribution (for calculation of C_f) and organ dryweights (for calculation of R_m) were the inputs to the model. Dry matter production (both level and dynamic behaviour) wassimulated reasonably well for most experiments, but final drymatter production was under-estimated by about 27% for the commerciallygrown crops. At low irradiance and with large crop dry weight,growth rate was under-estimated, probably as a result of over-estimationof R_m. This could almost completely explain the large under-estimationfor the commercially grown crops, which had large dry weight.Final dry matter production was over-estimated by 7-11% if dailyaverages instead of hourly input of climatic data were used. It is concluded that SUKAM is a reliable model for simulatingdry matter production in a tomato crop, except for those situationswhere R_m has a large influence on crop growth rate (low irradianceand large crop dry weight). An improved estimate of R_m wouldtake into account the influence of metabolic activity. A preliminaryattempt to relate maintenance costs to relative growth rate(a measure for metabolic activity), showed promising results.Copyright1995, 1999 Academic Press Crop growth, dry matter production, glasshouse, maintenance respiration, metabolic activity, model, relative growth rate, respiration, simulation, tomato, model validation     

Factors Controlling Induction of Carbonic Anhydrase and Efficiency of Photosynthesis in Chlorella vulgaris llh Cells

When Chlorella vulgaris llh cells which had been grown in airenriched with 2–4% CO₂ (high-CO₂ cells) were bubbled withair containing ca. 400 ppm CO₂, illumination at an intensityas low as the light compensation point (350 lux) was sufficientto increase the photosynthetic rate under limiting CO₂ concentrations.The same treatment induced carbonic anhydrase (CA) activity.The induction of CA activity and increase in photosyntheticrate at limiting CO₂ concentrations were observed in the presenceof 10 µM DCMU which completely inhibits photosynthesis.These results indicate that photosynthetic electron transportis not involved in CA induction in Chlorella vulgaris llh cells.The parallelism between the changes in CA activity and the rateof photosynthesis under limiting CO₂ concentrations agree withthe previous conclusion that the transport of CO₂ from outsideto the site of CO₂ fixation is facilitated by CA and hence lowersthe apparent K_m(CO₂) for photosynthesis. (Received December 24, 1982; Accepted May 10, 1983)     

Effects of Low Concentrations of Sulphur Dioxide on Net Photosynthesis and Dark Respiration of Vicia faba

Rates of net photosynthesis, P_N, and dark respiration of Viciafaba plants were measured in the laboratory in clean air andin air containing up to 175 parts 10^–9 (500 µg m^–3)SO₂. At all SO₂ concentrations exceeding 35 parts 10^–9,P_N was inhibited compared with clean air. At light saturation,the magnitude of inhibition depended on SO₂ concentration butat low irradiances the inhibition was independent of concentration.Dark respiration rates increased substantially, independentof concentration. When exposures continued for up to 3 days,P_N returned to clean air values about 1 h after fumigation ceased:dark respiration recovered after one photoperiod. There wereno visible injuries. Reviewing possible mechanisms responsible for the inhibitionof P_N, it is suggested that SO₂ competes with CO₂ for bindingsites in RuBP carboxylase. Analysis of resistance analoguesdemonstrates that SO₂ altered both stomatal and internal (residual)resistances. A model of crop photosynthesis shows the implications of theobserved responses for the growth of field crops in which plantsare assumed to respond like laboratory plants. Photosynthesisof the crop would be less sensitive than that of individualplants to SO₂ concentration. Daily dry matter accumulation ofhypothetical ‘polluted crops’ would be substantiallyless than clean air values but would vary relatively littlewith SO₂ concentration. It is concluded that physiological basesexist to account for observed reductions in growth of plantsat very low SO₂ concentrations, and that thresholds for plantresponses to SO₂ require reassessment.     

Effects of Light and CO2 on Net Photosynthesis Rates of Stands of Aubergine and Amaranthus

Net photosynthetic rates per unit ground area for plant standsof Solanum melongena L. var. esculentum (aubergine) and Amaranthuscaudatus L. var. edulis (grain amaranth) were measured over10 min intervals in an airtight, glass, controlled-environmentcabinet for a range of light flux densities provided by thediurnal variation in daylight. Light response curves for photosynthesisof stands, grown at ambient CO₂ concentration, were definedat 400, 800 and 1200 vpm CO₂. Light compensation points for these stands were around 20-30J m^-2 s^-1 and decreased slightly at higher CO₂ concentrations.For aubergine, a C₃ species, the short-term effects of CO₂ enrichmentwere to increase the initial slope as well as the asymptoteof the light response curve, reducing light saturation at moderateto high light flux densities; but for amaranthus, a C₄ species,saturation was less apparent and CO₂ enrichment scarcely increasedphotosynthesis except at light flux densities above 150 J m^-2s^-1. The canopies intercepted 93-98% of incident light. The efficiencyof utilization of intercepted light in photosynthesis (µgCO₂ J^-1) increased from zero at the light compensation pointto a maximum at an optimum light flux density of about 100 Jm^-2 s^-1 (the optimum rose a little with CO₂ enrichment) anddecreased slightly with further increase in light. Maximum utilizationefficiencies at 400 vpm CO₂ were 8-9 µg CO₂ J^-1. Enrichmentto 1200 vpm did not affect the peak utilization efficiency ofthe C₄ amaranthus, but increased that aubergine to 12·2µg CO₂ J^-1 (equivalent to some 14% when using the heatof combustion of plant dry matter to convert to the dimensionlessform). This is among the highest recorded efficiencies of lightutilization for stands, and relates to the exceptionally favourableenvironment, with optimal control of CO₂ concentration, humidity,temperature, water supply and mineral nutrition.Copyright 1993,1999 Academic Press Amaranthus caudatus L. var. edulis, Solanum melongena L. var. esculentum, canopy photosynthesis, CO₂ enrichment, light interception, light utilization, photosynthetic efficiency     

Estimation of Photorespiration of Green Plants and of their Mesophyll Resistance to CO2 Uptake

An estimate of photorespiration is obtained from the relationshipbetween the net exchange of CO₂ of the leaf and the internalCO₂ concentration, i.e. within the mesophyll intercellular spaces.The latter is obtained by calculation, taking into account thecombined epidermal and boundary-layer resistances between thebulk atmosphere and the mesophyll intercellular spaces. Thelinear part of this relationship (at low CO₂ concentrations)is extrapolated to zero internal concentration, at which noneof the intercellular photorespired CO₂ is available for reassimilation.The calculated output of CO₂ under such conditions providesan estimate of photorespiration, but, by failing to take intoaccount intracellular reassimilation of photorespired CO₂ underestimatesactual photorespiration. As the slope of this linear relationshiprepresents the mesophyll (intracellular) resistance to CO₂ uptake,this procedure was used to recalculate published data on effectsof light intensity and of oxygen concentration on net photosynthesis.The analysis showed that increased oxygen concentration anddecreased light intensity reduced photosynthesis largely byincreasing mesophyll resistance to CO₂ uptake. It is suggestedthat the CO₂ compensation point () is a function of both photorespiration(L) and mesophyll resistance (r_m): = L. r_m.     

Validation of a Photosynthesis Model through the Use of the CO2Balance of a Greenhouse Tomato Canopy

Several leaf photosynthesis models were developed from wellcontrolled experiments in growth chambers. However, only a fewhave been validated under greenhouse conditions for their quantitativeand qualitative adequacy. In this paper, rates of net photosynthesisfor a tomato crop (Lycopersicon esculentum Mill) were measuredin a semi-commercial greenhouse (615 m³) for a significant timeperiod. Concomitant measurements of climatic conditions andLAI were used for simulation of net photosynthesis using theTOMGRO model which integrates Acock's model for photosynthesiscalculations. From simulations and from sensitivity analysis,the prediction of net photosynthesis appeared to be very sensitiveto the quantum use efficiency. The Acock model with originalparameters underestimated the net photosynthesis rate, but anincrease in the quantum use efficiency by 10% gave a good fit.In an effort to generalize the validity of the model, a residualanalysis was performed and showed a systematic bias relatedto light intensity intercepted by the canopy. The Marquardtalgorithm was used to adjust our data to the model but did noteliminate residual heterogeneity of variance with new parametervalues. On the basis of collected data, the criteria of goodnessof fit used showed that the photosynthesis model is inadequatein describing the CO₂-balance of the greenhouse agrosystem.However, it was determined that it could be used as a submodelwithin a more complex model for predicting growth and development.Copyright 1999 Annals of Botany Company Greenhouse, CO₂-balance, photosynthesis, TOMGRO model, Acock's model, residuals, tomato Lycopersicon esculentum Mill.     

Growth Response of a Chrysanthemum Crop to the Environment. III, Effects of Radiation and Temperature on Dry Matter Partitioning and Photosynthesis

Vegetative crops of chrysanthemum were grown for 5 or 6 weekperiods in daylit assimilation chambers. Crop responses to differentradiation levels and temperatures were analysed into effectson dry matter partitioning, specific leaf area, leaf photosynthesisand canopy light interception. The percentage of newly formed dry matter partitioned to theleaves was almost constant, although with increasing radiationor decreasing temperature, a greater percentage of dry matterwas partitioned to stem tissue at the expense of root tissue.There was a positive correlation between the percentage of drymatter in shoot material and the overall carbon: dry matterratio. Canopy photosynthesis was analysed assuming identical behaviourfor all leaves in the crop. Leaf photochemical efficiency wasonly slightly affected by crop environment. The rate of grossphotosynthesis per unit leaf area at light saturation, P_A (max),increased with increasing radiation integral, but the same parameterexpressed per unit leaf dry matter, P_w (max) was almost unaffectedby growth radiation. In contrast, P_A (max) was hardly affectedby temperature but P_w (max) increased with increasing growthtemperature. This was because specific leaf area decreased withdecreasing temperature and increased with decreasing radiation.There was a positive correlation between canopy respirationintegral and photosynthesis integral, and despite a four-foldchange in crop mass during the experiments, the maintenancecomponent of canopy respiration remained small and constant. Canopy extinction coefficient showed no consistent variationwith radiation integral but was negatively correlated with temperature.This decrease in the efficiency of the canopy at interceptingradiation exactly cancelled the increase in specific carbonassimilation rate that occurred with increasing growth temperature,giving a growth rate depending solely on the incident lightlevel. Chrysanthemum, dry matter partitioning, photosynthesis, specific leaf area     

Influence of Temperature and O2 Concentration on Photosynthesis and Light Activation of Ribulosebisphosphate Carboxylase Oxygenase in Intact Leaves of White Clover (Trifolium repens L.)

Detached leaves of white clover (Trifolium repens L.) were keptfor 1 h under various conditions of temperature, oxygen concentrationand light intensity. Rates of photosynthesis were measured whereappropriate and then ribulosebisphosphate carboxylase oxygenase(RuBPCO) was extracted rapidly and its initial activity measuredimmediately. The extracted activity increased with increased intensity ofillumination of the leaves. Where leaves were pretreated atlow light intensity, the lower the temperature of the leavesthe higher the extracted activity of RuBPCO. At high light intensitytemperature did not affect the activity of subsequently extractedRuBPCO but the light intensity which was necessary for maximumactivity increased with temperature. Activity of RuBPCO fromleaves pretreated in the dark was least when CO₂ was low andtemperature high. Leaves, pretreated at low temperatures andhigh light intensity in 20% O₂, yielded higher activity in extractsthan leaves pretreated under similar conditions but in 2% O₂.A relatively weak temperature response of photosynthesis atlow irradiances was associated with a decrease in extractableRuBPCO activity with increasing temperature. A strong temperaturedependence of the oxygen inhibition of photosynthesis was associatedwith lower extractable RuBPCO activity in leaves pretreatedat low oxygen concentration at low temperatures. With leavesfrom plants grown at low temperatures prior to treatment ofleaves, oxygen inhibition of photosynthesis was less temperaturedependent and activity of RuBPCO in extracts was not decreasedby low O₂ at low temperatures. Differences in the activationof RuBPCO appear to influence photosynthesis and account foran absence of oxygen inhibition of photosynthesis at low temperaturesin plants grown in warm conditions. Key words: Ribulosebisphosphate carboxylase oxygenase activation, Photosynthesis, Temperature, O₂ effect, White clover     

The Effect of Light Intensity on the Release of Ethylene from Leaves

When leaf discs of Xanthium strumarium L. a C₃ plant, or Zeamays L. a C₄ plant, are incubated in 1-aminocyclopropane-l-carboxylicacid (ACC) in closed flasks, ethylene is released. The rateof ethylene release appears to be dependent on the levels oflight and CO₂ available for photosynthesis in the tissues. In Xanthium the rate of ethylene release is lower in the lightthan in the dark regardless of the presence or absence of addedbicarbonate as a source of CO₂. The inhibition of ethylene releaseis most apparent in the absence of added bicarbonate (i.e. atthe CO₂ compensation point), and at light intensities sufficientto saturate photosynthesis (had the CO₂ level in the test flaskbeen maintained). In contrast, light dramatically promotes therate of ethylene release from Zea leaf tissue when the CO₂ levelis maintained above the CO2 compensation point. The rate ofethylene release from either Xanthium or Zea, incubated withor without added bicarbonate, does not appear to be alteredby further increasing the light intensity above the minimallevels sufficient to saturate photosynthesis. In the closed system used in these studies and at a light intensitysufficient to saturate photosynthesis, Xanthium and Zea leaftissue both appear to release comparable amounts of ethylenefrom ACC when the data is expressed on a chlorophyll basis.However, in Xanthium the rate of ethylene release is similarin light and dark, while in Zea the rate in the light is muchgreater than in the dark when the data is expressed either ona leaf area or on a chlorophyll basis. It is suggested thatthe different responses of these tissues to light/dark transientsmay reflect differences in their ability to metabolize ACC and/ordifferences in their ability to retain and metabolize ethyleneitself.     

Photosynthetic Changes in the Inducible CAM Plant Sedum telephium L. Following the Imposition of Water Stress. 1. General Characteristics

The effects of water stress (drought) on the pattern of photosynthesisin Sedum telephium have been determined. Well-watered plantsexhibit a weak-CAM pattern, with substantial CO₂ fixation inthe day, a low level of CO₂ fixation at night, high daytimestomatal conductance with a lower conductance at night, andno diurnal fluctuation in acid content. Imposition of water-stress causes a switch from weak-CAM toa full-CAM mode of photosynthesis, as indicated by cessationof daytime CO₂ fixation, a marked increase in night-time CO₂fixation, very low daytime stomatal conductance, increased night-timeconductance and significant diurnal fluctuations in acid content. Sedum telephium, CAM, CO₂ fixation, drought, malate, photosynthesis, water stress     

Reactions of birch leaves to changes in light during early ontogeny: comparison between in vivo and in vitro techniques to measure carbon uptake

Trends in several photosynthetic parameters and their responseto changed growth light were followed for 15 d in leaves ofyoung birch saplings using a rapid-response gas exchange measuringequipment. These in vivo measurements were compared to biochemicalassays that were made from the same leaves after the gas exchangestudies. The measurements were made on leaves that were selectedprior to the study and were at that time of similar age. Forthe first 7 d the photosynthetic parameters were followed fromthe growth conditions of moderate light (200 µmol m^–2s^–1; referred to as controls later in the text). On day7 some of the saplings were transferred to grow either underhigh (450 µmol m^–2 s^–1; referred to as highlight plants) or low (75 µmol m^–2 s^–1; referredto as low light plants) light and the capability of the preselectedleaves for acclimation was followed for 6 d. For comparison,at the end of the experiment the measurements were made on bothcontrols and on young leaves that had developed under high andlow light. Generally the in vivo measured rate of CO₂ uptake (gross photosynthesis)both at 310 ppm CO₂ and 2000 ppm CO₂ corresponded very wellto the biochemically determined CO₂ fixation capacity in vitroafter rapid extraction (measured as the initial and total activityof Rubisco, respectively). However, if the flux of CO₂ intothe chloroplasts was limited by the closure of the stomata,as was the case of the high light plants, then the in vitromeasured Rubisco activity was greater than the in vivo measuredCO₂ uptake. V_max, calculated from the mesophyll conductanceat 1% O₂, exceeded the initial activity of Rubisco (assayedat saturating RuBP and CO₂) constantly by 60%. The catalyticactivity of Rubisco in birch leaves was overall very low, evenwhen calculated from the total activity of Rubisco (K_cat 0.63–1.18 s^–1), when compared to herbaceous C₃ species. Signs of light acclimation were not observed in most of thephotosynthetic parameters and in chloroplast structure whenmature birch leaves were subjected to changes in growth lightfor 6 d. However, the change of the growth light either to highor low light caused day-to-day fluctuations in most of the measuredphotosynthetic parameters and in the case of the high lightplants signs of photoinhibition and photodestruction were alsoobserved (decrease in the amount of chlorophyll and increasein chlorophyll a/b ratio). As a result of these fluctuationsthese plants achieved a new and lower steady-state conditionbetween the light and dark reactions, as judged from the molarratio of RuBP to Rubisco binding site. Key words: Acclimation, photosynthesis, light, Rubisco, birch     

Elevated atmospheric CO2 concentration ameliorates effects of NaCl salinity on photosynthesis and leaf structure of Aster tripolium L.

This study investigated the interaction of NaCl-salinity andelevated atmospheric CO₂ concentration on gas exchange, leafpigment composition, and leaf ultrastructure of the potentialcash crop halophyte Aster tripolium. The plants were irrigatedwith five different salinity levels (0, 25, 50, 75, 100% seawatersalinity) under ambient and elevated (520 ppm) CO₂. Under salineconditions (ambient CO₂) stomatal and mesophyll resistance increased,leading to a significant decrease in photosynthesis and wateruse efficiency (WUE) and to an increase in oxidative stress.The latter was indicated by dilations of the thylakoid membranesand an increase in superoxide dismutase (SOD) activity. Oxidativestress could be counteracted by thicker epidermal cell wallsof the leaves, a thicker cuticle, a reduced chlorophyll content,an increase in the chlorophyll a/b ratio and a transient declineof the photosynthetic efficiency. Elevated CO₂ led to a significantincrease in photosynthesis and WUE. The improved water and energysupply was used to increase the investment in mechanisms reducingwater loss and oxidative stress (thicker cell walls and cuticles,a higher chlorophyll and carotenoid content, higher SOD activity),resulting in more intact thylakoids. As these mechanisms canimprove survival under salinity, A. tripolium seems to be apromising cash crop halophyte which can help in desalinizingand reclaiming degraded land. Key words: Aster tripolium, cash crop halophyte, elevated CO₂, gas exchange, oxidative stress, photosynthesis, salt tolerance, ultrastructure, water use efficiency Received 29 July 2008; Revised 8 October 2008 Accepted 9 October 2008     

Photosynthesis and Transpiration in Rice as Influenced by Soil Moisture and Air Humidity

The paper describes the effect of soil moisture content andair humidity on CO₂ exchange (P_N), CO₂ diffusion resistance(Cr) and transpiration (E) in four varieties of japonica rice(Oryza sativa L.). A decrease in soil moisture content reducedthe rate of photosynthesis to a varying degree in the varieties.Reduction in photosynthesis was attributed to increase in Cr.The effect of low soil moisture on photosynthesis and CO₂ diffusionwas further intensified by decrease in air humidity. By maintaininga high humidity in the air around the leaves however, the effectof soil moisture deficiency was reduced considerably, exceptin Rikuto Norin 21 which was very sensitive to soil-moisturedeficiency alone. Dryness of the air enhanced the transpirationrate, although the increase was relatively less in the plantsfacing a simultaneous water crisis at the root surface. In plantsgrowing under flooded conditions, a decrease in air humiditycaused a slight depression in P_N despite the simultaneous decreasein Cr. Oryza sativa L., rice, photosynthesis, transpiration, diffusion resistance, soil moisture, air humidity     

The Greenhouse Effect: Acclimation of Tomato Plants Growing in High CO2, Photosynthesis and Ribulose-1, 5-Bisphosphate Carboxylase Protein

Tomato plants were grown in solution culture in a controlledenvironment at 20 ?C with a 12 h photoperiod of 400 µmolquanta m^–2 s^–1 PAR with either normal ambient CO₂,approximately 340 vpm, or with 1000 vpm CO₂. The short- andlong-term effects of CO₂ enrichment on photosynthesis were determinedtogether with the levels of ribulose-1, 5-bisphosphate carboxylase(RuBPco) E.C. 4.1.1.39 [EC] protein and activity throughout leafdevelopment of the unshaded 5th leaf above the cotyledons. Thehigh CO₂ concentration during growth did not appreciably affectthe rate of leaf expansion or final leaf area but did increasethe fresh weight per unit area of leaf. With short-term CO₂enrichment, i.e. only during the photosynthesis measurements,the light-saturated photosynthetic rate (P_max) of young leavesdid not increase while those reaching full expansion more thandoubled their net rate of CO₂ fixation. However, with longerterm CO₂ enrichment, i.e. growing the crop in high CO₂, theplants did not maintain this photosynthetic gain. While theCO₂ concentration during growth did not affect the peak in P_maxmeasured in 300 vpm CO₂ or P_max in 1000 vpm CO₂, RuBPco proteinor its activity, the subsequent ontogenetic decline in theseparameters was greatly accelerated by the high CO₂ treatment.Compared with plants grown in normal ambient CO₂ the high CO₂grown leaves, when almost fully expanded, contained only approximatelyhalf as much RuBPco protein and P_max in 300 vpm CO₂ and P_maxin1000 vpm CO₂ were similarly reduced. The loss of RuBPco proteinmay be a major factor associated with the accelerated fall inP_max since it was close to that predicted from the amount andkinetics of RuBPco assuming RuBP saturation. In the oldest leavesexamined grown in high CO₂ additional factors may be limitingphotosynthesis since RuBPco kinetics marginally overestimatedP_max in 300 vpm CO₂ and the initial slope of photosynthesisin response to intercellular CO₂ was also less than expectedfrom the extractable RuBPco. Key words: Lycopersicon esculentum (Mill.) cv. Findon Cross, CO₂ enrichment, acclimation to high CO₂, photosynthesis, RuBPco protein and activity