Separation of Direct and Indirect Responses of Stomata to Light: Results from a Leaf Inversion Experiment at Constant Intercellular CO2 Molar Fraction

Previous work has shown that stomata respond directly to light,but it was not clear whether the only additional response isthrough CO₂, or whether some other metabolite is involved inthis response. Gas exchange experiments were done with normallypositioned and inverted leaves of Hedera helix to investigatethis problem. The macroscopic optical properties of the leavesand their anatomical structure were also studied. These experimentssnowed that there is no need to postulate the existence of amessenger other than CO₂ to explain the indirect response ofstomata to light. The experiments also showed that leaf inversionaffects both stomatal conductance and photosynthesis, and highlightthe difficulties involved in the interpretation of the effectof leaf inversion on stomata when stomatal conductance measurementsare not done concurrently with measurements of CO₂ flux densityand intercellular CO₂ molar fraction Key words: Hedera helix, ivy, gas exchange, leaf inversion, stomatal conductance, light, CO₂ flux density, photosynthesis     

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     

Stomatal Responses of Variegated Leaves to CO2 Enrichment

The responses of stomatal density and stomatal index of fivespecies of ornamental plants with variegated leaves grown attwo mole fractions of atmospheric CO₂ (350 and 700 µmolmol^-1) were measured. The use of variegated leaves allowed anypotential effects of mesophyll photosynthetic capacity to beuncoupled from the responses of stomatal density to changesin atmospheric CO₂ concentration. There was a decrease in stomataldensity and stomatal index with CO₂ enrichment on both white(unpigmented) and green (pigmented) leaf areas. A similar responseof stomatal density and index was also observed on areas ofleaves with pigmentation other than green indicating that anydifferences in metabolic processes associated with colouredleaves are not influencing the responses of stomatal densityto CO₂ concentrations. Therefore the carboxylation capacityof mesophyll tissue has no direct influence on stomatal densityand index responses as suggested previously (Friend and Woodward1990 Advances in Ecological Research 20: 59-124), instead theresponses were related to leaf structure. The stomatal characteristics(density and index) of homobaric variegated leaves showed agreater sensitivity to CO₂ on green portions, whereas heterobaricleaves showed a greater sensitivity on white areas. These resultsprovide evidence that leaf structure may play an important rolein determining the magnitude of stomatal density and index responsesto CO₂ concentrations.Copyright 1995, 1999 Academic Press Leaf structure, photosynthesis, stomatal conductance, CO₂, stomatal density, stomatal index     

Humidity Pretreatment Affects the Responses of Stomata and CO2 Assimilation to Vapor Pressure Difference in C3 and C4 Plants

Experiments were carried out to investigate the long-term influenceof humidity on the short-term responses of stomata and CO₂ assimilationto vapor pressure difference in Oryza sativa (rice, C₃ species)and Panicum maximum (green panic, C₄ species). Plants were grownfor four weeks in growth chambers set at 35% and 85% relativehumidity at 25C air temperature, 38+2 Pa CO₂ partial pressureand 1,700µmol m^-2s^-1 photon flux density. Soil was saturatedwith water in both humidity treatments. Low humidity pretreatmentscaused low leaf conductance and low rates of transpiration andCO₂ assimilation in O. sativa, but small changes in stomatalresponses to humidity and in CO₂ assimilation were found inP. maximum. From the short-term gas exchange experiments, itwas noted that the responsiveness of leaf conductance to vaporpressure difference were affected by humidity pretreatmentsin O. sativa, whereas unaffected in P. maximum. In O. sativameasurements of CO₂ assimilation as a function of internal CO₂partial pressure (A-Ci curve) indicated that low humidity pretreatmentsreduced the CO₂ assimilation at high internal CO₂ partial pressure,but the initial slope of the A-Ci curve was unaffected. Furthermore,plant characteristics such as total dry weight and leaf areaof plants subjected to low umidity were lower than plants subjectedto high humidity. The reductions in O. sativa, however, werelarger than in P. maximum. Stomatal frequency from low humiditygrown plant was higher than that from high humidity grown plantsin both species although there is no significant difference.The data indicated that if the short term inhibition of netCO₂ assimilation at a high vapor pressure difference was imposedduring vegetative growth, the photosynthetic biochemistry andthe resultant plant growth were largely depressed in O. sativa,a C₃ species. (Received May 26, 1992; Accepted November 2, 1992)     

Nocturnal Accumulation of Acid in Leaves of Wall Pennywort (Umbilicus rupestris) Following Exposure to Water Stress

Physiological responses to water stress (drought) have beeninvestigated in Umbilicus rupestris (wall pennywort) by comparingcontrol (well-watered) and draughted plants with respect to(i) diurnal fluctuations in the acid content of the leaves,(ii) CO₂ exchange patterns and (iii) stomatal conductance. Controlplants show no diurnal fluctuations in acid content, whereasafter 6 d of drought a clear CAM-type pattern (nocturnal acidificationfollowed by deacidification in the light) is observed. In controlplants, the CO₂ exchange pattern over a 24 h period is of atypical C-3 ‘square-wave’ type, with extensive CO₂uptake in the light and CO₂ output in the dark. In droughtedplants the day-time CO₂ uptake is confined to a morning ‘burst’,whilst night-time CO₂ output is markedly reduced. There is howeverno net noctural uptake of CO₂. In control plants, stomatal conductanceis high during the day (especially in the first half of theday) falling to a low level at the onset of darkness, and thenrising slowly through the remainder of the night. In droughtedplants, stomatal conductance is very low, except that thereis morning ‘burst’ of high conductance and a periodduring the night when conductance is higher than in controlplants. These results are discussed in relation to the response of U.rupestris to drought both in laboratory and in field conditions. Umbilicus rupestris, wall pennywort, CO₂ exchange, Crassulacean acid metabolism, drought, stomatal conductance, water stress     

植物气孔导度的机理模型

Ball-Berry气孔导度模型及其修正模型是评价植物叶片气孔调节的重要工具。该文从CO₂分子在叶片气孔中扩散这个最基本的物理过程出发, 应用物理学中的分子扩散和碰撞理论、流体力学与植物生理学等知识, 严格推导出叶片气孔导度的机理模型。利用美国Li-Cor公司生产的Li-6400光合作用测定仪控制CO₂浓度、湿度和温度, 测量了华北平原冬小麦(Triticum aestivum)的光响应数据和气孔导度数据。拟合结果表明: 推导的气孔导度机理模型较之Ball-Berry气孔导度模型和Tuzet等气孔导度模型, 能更好地描述冬小麦的气孔导度与净光合速率之间的关系。如果用气孔导度的机理模型耦合光合作用对光响应的修正模型, 则耦合模型可以很好地描述华北平原冬小麦叶片气孔导度对光强的响应曲线, 并可直接估算冬小麦的最大气孔导度和对应的饱和光强, 同时可以研究最大气孔导度是否与最大净光合速率同步的问题。拟合结果还表明: 冬小麦在30 ℃、560 μmol·mol^-1CO₂, 或在32 ℃、370 μmol·mol^-1CO₂条件下, 最大气孔导度与最大净光合速率并不同步。     

Stomatal responses to a range of variables in two tropical tree species grown with CO2 enrichment

Seedlings of Maranthes corymbosa (Blume) and Eucalyptus tetrodonta(F. Muell) were grown with or without CO₂ enrichment (700µmolCO₂ mol^–1 The response of stomatal conductance (g₂) toleaf drying, exogenous absclslc acid and calcium ions was investigatedin M. corymbosa. Reciprocal transfer experiments were also conductedwhereby plants were grown in one treatment and then transferredto the other before g, was measured. Stomatal conductance in M. corymbosa was more sensitive (a greaterpercentage decline in g₂ per unit percentage decline in leaffresh weight) to leaf water status under conditions of CO₂ enrichmentcompared to ambient conditions. However, the rate of reductionof g₂ in response to exogenous abscisic acid was not influencedby CO₂ treatment. In contrast, the rate of reduction of g₂,in response to exogenous CaCl₂ was decreased under conditionsof CO₂ enrichment. Reciprocal transfer experiments showed that expo sure to CO₂enrichment results in a short-term, reversible decline in g₂,as a result of decreased stomatal aperture and a long-term,irreversible decline in g₂ as a result of a decreased stomataldensity. Seedlings of E. tetrodonta were used to investigate the responseof g₂ to light flux density, leaf-to-air vapour pressure difference(LAVPD), leaf internal CO₂ concentration (C₁ and temperature.Reciprocal transfer experiments were also conducted. CO₂ enrichmentdid not influence the pattern or sensitivity of response ofg to LAVPD and C in E. tetrodonta. In contrast, the slope ofthe response of g₂, to temperature decreased for trees grownunder elevated [CO₂]_a conditions and the equilibrium g₂ attainedat saturating light was also decreased for plants grown underelevated [CO_2a. conditions. Key words: Stomata, elevated CO₂, tropical trees     

Evidence for the Occurrence of Feedback Inhibition of Photosynthesis in Rice

The response of photosynthesis in the flag leaf of rice (Oryzasativa) to elevated CO₂ or reduced O₂ was investigated relativeto other environmental factors using steady-state gas exchangetechniques. We found under moderate conditions of temperatureand photosynthetic flux density (PFD) (26°C and 700µmolquanta m^–2s^–1 similar to growth conditions) photosynthesisin the flag leaf of rice during heading and grain filling saturatedat near ambient levels of CO₂, with a concomitant loss of O₂sensitivity, when a high stomatal conductance was maintainedby high humidity (low vapor pressure deficit). Under 18°Cthere was near complete loss of O₂ sensitivity of photosynthesisat normal ambient levels of CO₂. This is in contrast to thelarge enhancement of photosynthesis by supra-atmospheric levelsof CO₂ and sub-atmospheric levels of O₂ by suppression of photorespirationwhen there is no limitation on utilizing the initial productof CO₂ assimilation (triose-P) as predicted from Ribulose-l,5-bisphosphatecarboxylase/oxygenase (Rubisco) kinetic properties. Thus, lossof sensitivity to CO₂ and O₂ has been previously explained asa limitation on utilization of triose-P to synthesize carbohydrates.Under high PFD at 25°C, the rate of photosynthesis in ricedeclined over a period of hours around midday, while the intercellularlevels of CO₂ remained constant suggesting a limitation on utilizationof photosynthate. Short-term fluctuations in climatic factorsincluding temperature, light and humidity could result in afeedback limitation on photosynthesis in rice which may be exacerbatedby rising CO₂. (Received March 12, 1998; Accepted May 14, 1998)     

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     

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     

Stomatal Characteristics of Four Native Herbs Following Exposure to Elevated CO2

Contrasting effects on the stomatal index (SI), stomatal density,epidermal cell size and number were observed in four chalk grasslandherbs (Sanguisorba minor Scop., Lotus corniculatus L., Anthyllisvulneraria L. and Plantago media L.) following exposure to elevatedcarbon dioxide concentrations (CO₂) in controlled environmentgrowth cabinets. SI of S. minor increased for both leaf surfaces,whilst in A. vulneraria and P. media SI decreased on one surfaceonly. In L. corniculatus , no differences in SI were observedas epidermal cell density changed in parallel with stomataldensity. In L. corniculatus and S. minor stomatal density increasedon both surfaces, whereas in P. media it decreased; in A. vulnerariastomatal density decreased on the abaxial leaf surface alonefollowing exposure to elevated CO₂. In the latter three species,SI changed because stomatal density did not change in parallelwith epidermal cell density. The results suggest elevated CO₂is either directly or indirectly affecting cell differentiationand thus stomatal initiation in the meristem. In S. minor and P. media leaf growth increased in elevated CO₂,because of increased cell expansion of epidermal cells, whereasin L. corniculatus, epidermal cell size decreased and greaterleaf growth was because of an increase in epidermal cell divisions.In A. vulneraria, leaf size did not change, but increased cellexpansion on the adaxial surface suggests CO₂ affects leaf surfacesdifferently, either directly or indirectly at the cell differentiationstage or as the leaf grows. These results suggest component species of a plant communitymay differ in their response to elevated CO₂. Predicting theeffect of environmental change is therefore difficult.Copyright1994, 1999 Academic Press Elevated CO₂, Sanguisorba minor (salad burnet), Lotus corniculatus (birdsfoot trefoil), Anthyllis vulneraria (kidney vetch), Plantago media (hoary plantain), stomatal index, stomatal density, epidermal cell size     

Elevated CO2and Temperature have Different Effects on Leaf Anatomy of Perennial Ryegrass in Spring and Summer

Mature second leaves of Lolium perenne L. cv. Vigor, were sampledin a spring and summer regrowth period. Effects of CO₂enrichmentand increased air temperature on stomatal density, stomatalindex, guard cell length, epidermal cell density, epidermalcell length and mesophyll cell area were examined for differentpositions on the leaf and seasons of growth. Leaf stomatal density was smaller in spring but greater in summerin elevated CO₂and higher in both seasons in elevated temperatureand in elevated CO₂xtemperature relative to the respective controls.In spring, leaf stomatal index was reduced in elevated CO₂butin summer it varied with position on the leaf. In elevated temperature,stomatal index in both seasons was lower at the tip/middle ofthe leaf but slightly higher at the base. In elevated CO₂xtemperature,stomatal index varied with position on the leaf and betweenseasons. Leaf epidermal cell density was higher in all treatmentsrelative to controls except in elevated CO₂(spring) and elevatedCO₂xtemperature (summer), it was reduced at the leaf base. Inall treatments, stomatal density and epidermal cell densitydeclined from leaf tip to base, whilst guard cell length showedan inverse relationship, increasing towards the base. Leaf epidermalcell length and mesophyll cell area increased in elevated CO₂inspring and decreased in summer. In elevated CO₂xtemperatureleaf epidermal cell length remained unaltered in spring comparedto the control but decreased in summer. Stomatal conductancewas lower in all treatments except in summer in elevated CO₂itwas higher than in the ambient CO₂. These contrasting responses in anatomy to elevated CO₂and temperatureprovide information that might account for differences in seasonalleaf area development observed in L. perenne under the sameconditions. Lolium perenne ; perennial ryegrass; elevated CO₂and temperature; stomatal density; stomatal index; cell size     

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     

The Responses of Stomatal Density to CO2 Partial Pressure

Experiments on a range of species of tree, shrub and herb haveshown that stomatal density and stomatal index increase as thepartial pressure of CO₂ decreases over the range from the currentlevel of 34 Pa to 22.5 Pa. Stomatal density responds to thereduced partial pressure of CO₂ in a simulation of high altitude(3000 m), when the CO₂ mole fraction is unchanged. When the partial pressure of CO₂ is increased from 35 to 70Pa stomatal density decreases slightly, with a response to unitchange in CO₂ which is about 10% of that below 34 Pa. Measurements of gas exchange on leaves which had developed indifferent CO₂ partial pressures, but at low saturation vapourpressure deficits in the range of 0.7 to 0.9 kPa, indicatedlower photosynthetic rates but higher stomatal conductancesat reduced CO₂ partial pressures. Experiments on populations of Nardus stricta originating fromaltitudes of 366 m and 810 m in Scotland, indicated geneticdifferences in the responses of stomatal density to CO₂ in pressuressimulating altitudes of sea level and 2 000 m. Plants from thehigher altitude showed greater declines in stomatal densitywhen the CO₂ partial pressure was increased. Key words: Stomata, CO₂, gas exchange, altitude, atmospheric pressure     

Effect of Elevated CO2 on Stomatal Density and Distribution in a C4 Grass and a C3 Forb under Field Conditions

Two common tallgrass prairie species, Andropogon gerardii, thedominant C₄ grass in this North American grassland, and Salviapitcheri, a C₃ forb, were exposed to ambient and elevated (twiceambient) CO₂ within open-top chambers throughout the 1993 growingseason. After full canopy development, stomatal density on abaxialand adaxial surfaces, guard cell length and specific leaf mass(SLM; mg cm^-2) were determined for plants in the chambers aswell as in adjacent unchambered plots. Record high rainfallamounts during the 1993 growing season minimized water stressin these plants (leaf xylem pressure potential was usually >-1·5 MPa in A. gerardii) and also minimized differencesin water status among treatments. In A. gerardii, stomatal densitywas significantly higher (190 ± 7 mm^-2; mean ±s.e.) in plants grown outside of the chambers compared to plantsthat developed inside the ambient CO₂ chambers (161 ±5 mm^-2). Thus, there was a significant 'chamber effect' on stomataldensity. At elevated levels of CO₂, stomatal density was evenlower (P < 0·05; 121 ± 5 mm^-2). Most stomatawere on abaxial leaf surfaces in this grass, but the ratio ofadaxial to abaxial stomatal density was greater at elevatedlevels of CO₂. In S. pitcheri, stomatal density was also significantlylower when plants were grown in the open-top chambers (235 ±10 mm^-2 outside vs. 140 ± 6 mm^-2 in the ambient CO₂ chamber).However, stomatal density was greater at elevated CO₂ (218 ±12 mm^-2) compared to plants from the ambient CO₂ chamber. Theratio of stomata on adaxial vs. abaxial surfaces did not varysignificantly in this herb. Guard cell lengths were not significantlyaffected by growth in the chambers or by elevated CO₂ for eitherspecies. Growth within the chambers resulted in lower SLM inS. pitcheri, but CO₂ concentration had no effect. In A. gerardii,SLM was lower at elevated CO₂. These results indicate that stomataland leaf responses to elevated CO₂ are species specific, andreinforce the need to assess chamber effects along with treatmenteffects (CO₂) when using open-top chambers.Copyright 1994, 1999Academic Press Andropogon gerardii, elevated CO₂, Salvia pitcheri, stomatal density, tallgrass prairie     

Response of Photosynthesis, Stomatal Conductance and Water Use Efficiency to Elevated CO2 and Nutrient Supply in Acclimated Seedlings of Phaseolus vulgaris L.

Plants of Phaseolus vulgaris L were grown from seed in open-topgrowth chambers at present day (350 µmol mol^–1)and double the present day (700 µmol mol^–1) atmosphericCO₂ concentration with either low (L, without additional nutrientsolution) or relatively high (H, with additional nutrient solution)nutrient supply Measurements of assimilation rate, stomatalconductance and water use efficiency were started 17 d aftersowing on each fully expanded, primary leaf of three plantsper treatment Measurements were made in external CO₂ concentrations(C₂) of 200, 350, 450, 550 and 700 µmol mol^–1 andrelated to both C_a and to C₁, the mean intercellular space CO₂concentration Fully adjusted, steady state measurements weremade after approx 2 h equilibration at each CO₂ concentration The rate of CO₂ assimilation by leaves increased and stomatalconductance decreased similarly over the range of C_a or C₁ inall four CO₂ and nutrient supply treatments but both assimilationrate and stomatal conductance were higher in the high nutrientsupply treatment than in the low nutrient treatment The relationbetween assimilation rate or stomatal conductance and C₁ wasnot significantly different amongst plants grown in present-dayor elevated CO₂ concentration in either nutrient supply treatment,i e there was no evidence of down regulation of photosynthesisor stomatal response Increase in CO₂ concentration from 350to 700 µmol mol^–1 doubled water use efficiency ofindividual leaves in the high nutrient supply treatment andtripled water use efficiency in the low nutrient supply treatment The results support the hypothesis that acclimation phenomenaresult from unbalanced growth that occurs after the seed reservesare exhausted, when the supply of resources becomes growth limiting CO₂ enrichment, Phaseolus vulgaris L., net CO₂ assimilation rate, stomatal conductance, water use efficiency     

Growth at elevated CO2 leads to down-regulation of photosynthesis and altered response to high temperature in Quercus suber L. seedlings

The effects of growth at elevated CO₂ on the response to hightemperatures in terms of carbon assimilation (net photosynthesis,stomatal conductance, amount and activity of Rubisco, and concentrationsof total soluble sugars and starch) and of photochemistry (forexample, the efficiency of excitation energy captured by openphotosystem II reaction centres) were studied in cork oak (Quercussuber L.). Plants grown in elevated CO₂ (700 ppm) showed a down-regulationof photosynthesis and had lower amounts and activity of Rubiscothan plants grown at ambient CO₂ (350 ppm), after 14 monthsin the greenhouse. At that time plants were subjected to a heat-shocktreatment (4 h at 45C in a chamber with 80% relative humidityand 800–1000 mol m^–2 s^–1 photon flux density).Growth in a CO₂-enriched atmosphere seems to protect cork oakleaves from the short-term effects of high temperature. ElevatedCO₂ plants had positive net carbon uptake rates during the heatshock treatment whereas plants grown at ambient CO₂ showed negativerates. Moreover, recovery was faster in high CO₂-grown plantswhich, after 30 min at 25C, exhibited higher net carbon uptakerates and lower decreases in photosynthetic capacity (A_max aswell as in the efficiency of excitation energy captured by openphotosystem II reaction centres (F_vJF_m than plants grown atambient CO₂. The stomata of elevated CO₂ plants were also lessresponsive when exposed to high temperature. Key words: Elevated CO₂, temperature, acclimation, photosynthesis, Quercus suber L.     

Effects of CO2 Enrichment on Four Poplar Clones. II. Leaf Surface Properties

The poplar clones Columbia River, Beaupre, Robusta and Raspaljehave been investigated in the present (350 µmol mol^–1)and double the present (700 µmol mol^–1) atmosphericCO₂ concentration. Cuttings were planted in pots and were grownin open-top chambers inside a glasshouse for 92 d. Stomatal density, stomatal index, length of stomatal pore andepidermal cell density were not affected by CO₂ enrichment inany of the clones. Lack of differences in stomatal density orindex indicate that there were no direct effects of CO₂ enrichmenton the initiation of the number of stomata during ontogenesisor on epidermal cell expansion at a later stage. Stomatal conductance decreased because of the effect of CO₂on stomatal opening. The average reduction in both adaxial andabaxial surface has been estimated at 41%. Beaupre showed thelargest response of stomatal conductance and Columbia Riverthe smallest. Poplar clones, CO₂ enrichment, stomatal density, stomatal length, stomatal conductance     

The Effect of Vapour Pressure Deficit on Carbon Isotope Discrimination in the Desert Shrub Larrea tridentata(Creosote Bush)

Larrea tridentata (creosote bush) seedlings were subjected tothree regimens of atmospheric humidity in a growth chamber experiment.Relative humidity was varied to achieve daytime vapour pressuredeficits (VPD) during growth of 29, 48 and 77 kPa. Photosyntheticgas exchange, carbon isotope composition and biomass productionwere measured after 8–10 weeks of treatment. Whereas stomatalconductance (g) declined linearly with increasing ambient VPD,CO₂ assimilation rate (A) was not measurably affected by changesin ambient VPD. This resulted in a decrease in intrinsic wateruse efficiency (ratio of CO₂ assimilation to stomatal conductance;A/_g) with increasing VPD. Leaf carbon isotope discrimination(A) was negatively correlated (r² = 088) with A/g ratios. Carbonisotope discrimination also correlated positively with ratiosof internal (C₁) to ambient (c_a) CO₂ levels determined by gasexchange measurements (c₁/c). The ratio of c₁ to c_a was lowerat higher VPD levels. Leaf biomass decreased with increasingambient VPD and correlated positively with. Root to leaf biomassratio increased at higher VPD levels and correlated negativelywith. Key words: Larrea tridentata, vapour pressure deficit, carbon isotope discrimination, intrinsic water-use efficiency     

Acclimation of Lolium temulentum to enhanced carbon dioxide concentration

Acclimation of single plants of Lolium temulentum to changing[CO₂] was studied on plants grown in controlled environmentsat 20°C with an 8 h photoperiod. In the first experimentplants were grown at 135 µ;mol m^–2 s^–1 photosyntheticphoton flux density (PPFD) at 415µl l^–1 or 550µll^–1 [CO₂] with some plants transferred from the lowerto the higher [CO₂] at emergence of leaf 4. In the second experimentplants were grown at 135 and 500 µmol m^–2 s^–1PPFD at 345 and 575 µl l^–1 [CO₂]. High [CO₂] during growth had little effect on stomatal density,total soluble proteins, chlorophyll a content, amount of Rubiscoor cytochrome f. However, increasing [CO₂] during measurementincreased photosynthetic rates, particularly in high light.Plants grown in the higher [CO₂] had greater leaf extension,leaf and plant growth rates in low but not in high light. Theresults are discussed in relation to the limitation of growthby sink capacity and the modifications in the plant which allowthe storage of extra assimilates at high [CO₂]. Key words: Lolium, carbon dioxide, photosynthesis, growth, stomatal density