Effects of CO2-Enrichment on the Growth of Young Tomato Plants in Low Light

Carbon dioxide-enrichment of young tomato plants grown in controlled-environmentcabinets at low light intensity (14 cal cm^–2 day^–1,visible radiation) increased their net assimilation rates and,initially, relative growth-rates. Subsequently, the relativegrowth-rate fell to near the rate of non-enriched plants, owingto a fall in leaf-area ratio associated with an increase inleaf dry weight/area. Sowing non-enriched plants a few daysearlier to reach the same total dry weight would not have producedidentical plants. The effects of CO₂-enrichment to 1000 vpm could be simulatedby increasing light intensity by approximately one third exceptthat the plants had shorter internodes than those in extra CO₂.This was a morphogenetic effect of light since CO₂-enrichmentitself produced slightly shorter plants than controls for anequivalent total dry weight. CO₂-enrichment did not change the dry-weight distribution inthe plants and had little effect on rate of leaf produoctionor the number of flower primordia. There were no indicationsthat beneficial effects of CO₂-enrichment operated other thanthrough increased photosynthesis.     

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 Influence of Carbon Dioxide and Daily Photon-flux Density on Optimal Leaf Nitrogen Concentration and Root: Shoot Ratio

Using a cost-benefit model, the leaf nitrogen concentrationand root : shoot ratio that maximize whole-plant relative growthrate are determined as a function of the above-ground environment(integrated daily photon flux density and the concentrationof carbon dioxide at the site of fixation within the leaf).The major advantage of this approach is that it determines theadaptive significance of leaf physiology by considering thefunctional integration of leaves and roots. The predicted responseto increasing daily photon flux densities is an increase inoptimal leaf N concentration (N_opt) and a concomitant increasein root: shoot ratio. Increased carbon dioxide concentrations,on the other hand, reduce N_opt and only slightly change root:shoot ratio. The observed increase in leaf nitrogen concentrationfound in plants growing at high altitudes (low CO₂ partial pressure)is also predicted. Since these responses to light and CO₂ maximizethe whole-plant relative growth rate, the observed adjustmentsthat plants make to light and carbon dioxide concentration appearto be adaptive. We show that the relationship between photosynthesis and leafnitrogen concentration is complex and depends on the light andCO₂ levels at which photosynthesis is measured. The shape ofthis function is important in determining N_opt and the oppositeresponse of leaf nitrogen to light and carbon dioxide is shownto be the result of the different effects of light and CO₂ onthe photosynthesis-leaf nitrogen curve. Plant growth, photosynthesis, leaf nitrogen, biomass allocation, optimization, carbon dioxide light     

Effect of Nitrogen Supply on the Photosynthetic Performance of Leaves from Coffee Plants Exposed to Bright Light

Although Coffea arabica L. grows naturally in shaded habitats,it can be cultivated under high light intensity, but not withoutsevere photoinhibition mainly during the period of transferfrom the nursery into the field. The present work examines someof the changes in the photosynthetic performance induced byexposure to high light and the possibility of using enhancednitrogen levels to overcome photoinhibition. For that purpose,young plants of Coffea arabica L. (cv. Catuai) grown in a shadedgreenhouse were treated with 0, 1 and 2 mmol of nitrogen and4 weeks later exposed to full solar irradiation, outside. Visible damage due to exposure to full sunlight appeared within2 d in all plants, resulting in a reduced photosynthetic leafarea and drastic shedding of leaves in the unfertilized plants.These effects were considerably less in plants with the highestN dose. After 130 d of exposure, there was 100% mortality inplants receiving no extra nitrogen, compared with 30% in theplants treated with 2 mmol nitrogen. Photosynthesis rates, leafconductance and transpiration presented minimum values after4 d of light stress. Large changes in the photosynthetic capacity(measured at high CO₂ concentration and high light intensity),quantum efficiency and fluorescence yield (F_v/F_m) indicate thatnet photosynthesis rate in the air had been reduced by bothstomatal closure and by changes at the photochemical level.All indicators show that N-fertilized plants were less affectedby photoinhibition. Key words: Coffee plant, nitrogen, photoinhibition, photosynthesis     

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     

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.     

不同植物叶片水分利用效率对光和CO2的响应与模拟

植物叶片水分利用效率的高低取决于气孔控制的光合作用和蒸腾作用两个相互耦合的过程,模拟水分利用效率对环境变化的响应特征和机制是理解生态系统碳循环和水循环及其耦合关系的基础.研究通过人工控制光强和CO2浓度,对叶片水分利用效率进行了研究.提出了植物水分利用效率在光强和CO2浓度共同作用下的估算模型.数据分析表明,该模型在包括C3和C4植物、草本和木本植物在内的9种植物上能很好地模拟水分利用效率对光强和CO2浓度共同作用的响应.该模型可以用于估算CO2浓度升高条件下光合速率的提高和蒸腾速率的降低对水分利用效率提高的贡献量.CO2浓度变化条件下,水分利用效率在不同植物之间有巨大差异,研究区域尺度植物的水分利用效率时至少需要将植物区分为C4植物和C3植物,其中C3植物区分为草本和木本植物3种生态功能型才能较为准确地估算植物的整体水分利用效率.应用本研究提出的水分利用效率估算模型和植物水分利用效率生态功能型分类标准,可以为建立以植物的水分利用效率为基本参数的陆地生态系统水循环模型和陆地生态系统生产力模型提供重要依据.     

Responses of water use efficiency of 9 plant species to light and CO2 and their modeling

Photosynthesis coupled with transpiration determines water use efficiency (WUE) at leaf level, and the responses of WUE controlled by gas exchanges through stomata to environment are the basis of carbon and water cycles in the ecosystem. In this paper, by using Li-6400 Portable Photosynthesis System (LI-COR), WUE at leaf level was analyzed under controlled photosynthetic photons flux density (PPFD) and CO₂ concentration conditions across 9 plant species including maize (Zea mays), sorghum (Sorghum vulgare), millet (Setaria italica), soybean (Glycine max), peanut (Arachis phyogaea), sweet potato (Ipomoea batatas), rice (Oryza sativa), Masson pine (Pinus massoniana) and Schima superba. We had developed a new model to estimate the water use efficiency in response to the combined effects of light and CO₂ concentration. Our measured data validated that this model could simulate the changes of water use efficiency very well under combined effect of light and CO₂ concentration. It could be used to estimate contribution of photosynthesis increase and transpiration decline on water use efficiency with the rising of CO₂ concentration. Great differences in water use efficiency occurred in these different plant species under various CO₂ concentration levels. Based on water use efficiency at regional scale, we concluded that plants should be separated into C₃ plants and C₄ plants, and furthermore, C₃ plants should be separated into herbaceous plants and woody plants. Our separation criteria would do a great favor in modeling the evapotranspiration of terrestrial ecosystem with carbon and water balance.     

Effects of Different Nitrogen Sources and Concentrations on CAM Photosynthesis in Kalanchoe blossfeldiana

When Kalanchoë blossfeldiana Poelln. cv. Hikan plants werecultured in solutions containing 0.2, 1.0, 5.0 or 10 mM of nitrateor ammonium under a long-day photoperiod, some criteria of CAM(Crassulacean acid metabolism) photosynthesis (diurnal changesof CO₂ uptake, titratable acidity and malate content in leaves)were examined. The plants absorbed 90 to 100% of CO₂ duringthe light phase regardless of the supplied nitrogen. Nitrate-grownplants absorbed about 10% of CO₂ during the dark phase regardlessof the supplied concentration, whereas in ammonium-grown plantsthe nocturnal CO₂ uptake occurred at 0.2 mM, at which the plantsdepleted nitrogen and no uptake was observed at the higher concentrations.Changes of nocturnal increase in titratable acidity and malatecontent almost corresponded with the changes in the amount ofnocturnal CO₂ uptake. Also K. daigremontiana plants suppliedwith 10 mM of ammonium had a less CAM-like pattern of diurnalCO₂ uptake than the plants supplied with 10 mM of nitrate. Theseresults suggest that a sufficient supply of ammonium depressesCAM photosynthesis.     

Responses of shoot and root gas exchange, leaf blade expansion and biomass production to pulses of elevated C02 in hydroponic wheat

Short-term effects of elevated CO₂ during the early life phaseof plants may have long lasting consequences for growth andbiomass in later periods. We exposed hydroponically grown wheatseedlings to 5 d pulses of elevated CO₂ while leaf expansiongrowth as well as shoot and root gas exchange were measuredsimultaneously and continuously. Shoot photosynthesis, night-timeshoot respiration and below-ground respiration (largely by roots)roughly doubled when atmospheric CO₂ concentration was doubled.An interruption of CO₂ enrichment caused CO₂ assimilation andrespiration to return to control levels. However, while theresponse of photosynthesis was immediate, that of respirationshowed a hysteresis of about 3 d. Since shoot biomass increasedat elevated CO₂ (with no change in allocation pattern) equalfluxes per shoot or root system after a return to control CO₂concentrations indicate substantial downward adjustment of thecapacity for CO₂ fixation and release in high-CO₂ grown plants.Leaf expansion growth was completely unaffected by CO₂ enrichment,whereas tiller initiation was significantly increased (doubledin 18 d). We conclude that leaf growth in these wheat plantswas already carbon-saturated at ambient CO₂ concentration atoptimum mineral nutrient supply. The stimulation of growth ofwhole plants was exclusively due to enhanced tillering duringthis very early part of the life of these wheat plants. Key words: Allocation, atmospheric carbon dioxide enrichment, growth, photosynthesis, respiration, tillering, Triticum aestivum     

Effect of Temperature on Photosynthesis and Photorespiration of Wheat Leaves

Wheat plants were grown in a controlled environment with daytemperatures of 18 ?C and with 500 µ Einsteins m^–28^–1 of photosynthetically active radiation for 16 h. Beforeanthesis and 2 to 3 weeks after, rates of net photosynthesiswere measured for leaves in 2 or 21% O₂ containing 350 vpm CO₂at 13, 18, 23, and 28 ?C and with 500 µEinsteins m^–2s^–1 of photosynthetically active radiation. Also, underthe same conditions of light intensity and temperature, therates of efflux of CO₂ into CO₂-free air were measured and,for mature flag leaves 3 to 4 weeks after anthesis, gross andnet photosynthesis from air containing 320 vpm ¹⁴CO₂ of specificactivity 39?7 nCi µmol^–1. When the O₂ concentration was decreased from 21 to 2% (v/v)the rate of net photosynthesis increased by 32 per cent at thelowest temperature and 54 per cent at the highest temperature.Efflux of CO₂ into CO₂-free air ranged from 38 per cent of netphotosynthesis at 13 ?C to 86 per cent at 28 ?C. Gross photosynthesis,measured by the ¹⁴C assimilated during 40 s, was greater thannet photosynthesis by some 10 per cent at 13 ?C and 17 per centat 28 ?C. These data indicate that photorespiration was relativelygreater at higher temperatures.     

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.     

Stomatal Opening in Light of Different Wavelengths: Effects of Blue Light Independent of Carbon Dioxide Concentration

Stomatal opening in Xanthium pennsylvanicum was found to besignificantly greater in blue light than in red. Experimentsin which leaves were placed in a closed system and allowed toestablish their own steady-state carbon dioxide concentrationshowed that when the CO₂ concentration was about the same asthat in red, opening was much greater in blue light. Blue lightof low intensity could cause as great an opening as red of higherintensity, even though the CO₂ concentration was much higherin blue. Stomatal opening in light is considered as involvingat least two reactions: (1) a response to the removal of CO₂by photosynthesis; (2) a response to blue light not dependenton the removal of CO₂. Blue light became increasingly effective, relative to red, asthe length of night was increased over the range 2 to 14 hours.This might, in part, explain previously observed effects ofnight length on rate of opening in light. The initial very rapid phase of closure in darkness appearedto be independent of CO₂ accumulation, for it was not preventedby flushing the intercellular spaces with air free of CO₂. Itis suggested that closure in darkness, like opening in light,should be considered as involving components both dependentupon, and independent of, CO₂ concentration.     

Effects of Temperature and CO2 Concentration on Induction of Carbonic Anhydrase and Changes in Efficiency of Photosynthesis in Chlorella vulgaris 11h

The increase in carbonic anhydrase (CA) activity and the decreasein apparent K_m(CO₂) for photosynthesis induced by reducing CO₂concentration during the growth of Chlorella vulgaris 11h cellswere followed under different temperatures. Both changes wereaccelerated by raising the temperature and reached an optimumat 32–37?C. When the CO₂ concentration was lowered from3 to 0.04%, the rate of photosynthetic O₂ evolution at limitingCO₂ concentrations increased and reached a stationary levelafter 3 h. Under such conditions, the concentration of CO₂ dissolvedin the algal suspension decreased logarithmically (t_1/2=10 min)and reached a concentration in equilibrium with 0.04% CO₂ inair after ca. 2 h. When high-CO₂ cells grown with 3% CO₂ in air were transferredto various lower CO₂ concentrations, CA activity and apparentK_m(CO₂) for photosynthesis changed depending on the CO₂ concentration.The CO₂ concentration which gives one-half the maximum valuefor K_m(CO₂) and one-half minimum value foi CA activities wasabout 0.5%. The inverse relationship observed for the changesin CA activity and the affinity for CO₂ in photosynthesis supportsthe theory that CA loweres the apparent K_m(CO₂) for photosynthesisin Chlorella vulgaris 11h. (Received August 27, 1984; Accepted February 8, 1985)     

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)     

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     

Photomorphogenesis, Photosynthesis, and Early Growth of Primary Leaves of Phaseolus vulgaris

The response of leaf tissue to white, blue, red, and far-redlight has been examined. Leaves on plants grown in darknessshow increased cell number, cell volume, and area when exposedto long periods (up to 48 h) of low-intensity red, blue, orfar-red radiation. This is believed to be a photomorphogenicresponse which does not involve photosynthesis. Leaves fromplants exposed to white light during germination do not usuallyrespond to red, blue, or far-red light. An exception to thiswas found for leaf discs which showed a larger increase in areathan the dark controls following exposure to far-red light for24 h. Leaf tissue from light-grown plants responds to high-intensitywhite light, probably through photosynthesis. Discs cut fromdark-grown plants and cultured in white light grow equally wellin air and CO₂-free conditions. Application of the photosyntheticinhibitor DCMU reduces growth and chlorophyll formation, however. It is concluded that light, perhaps acting through the phytochromemechanism, has initially a number of morphogenic effects includinginitiation of development of the photosynthetic apparatus. Theresponses to photomorphogenically active radiation do not persistand light effects through photosynthesis are rapidly initiatedand dominate the later stages of leaf growth.     

Stomatal and Mesophyll Limitations of Photosynthesis in Phosphate Deficient Sunflower, Maize and Wheat Plants

The effects of phosphate deficiency on the composition and photosyntheticCO₂ assimilation rates of fully expanded leaves of sunflower,maize and wheat plants are described. The regulation of photosynthesisby stomatal and mesophyll characteristics of leaves of differentphosphate status is analysed and related to structure. Phosphatedeficient leaves had small concentrations of inorganic phosphate,Pi, in the tissue water. Rate of photosynthesis in leaves andstomatal conductance were smaller in plants grown with inadequatephosphate when measured under any given light intensity or CO₂partial pressure. Despite the decrease in stomatal conductance(and without evidence of patchy stomatal closure), the relativestomatal limitation of photosynthesis was similar in the plantsgrown with deficient or abundant phosphate. However, the mesophyllcapacity for photosynthesis was greatly limited by phosphatedeficiency. Leaves deficient in phosphate had larger numbersof small size cells per unit leaf area than leaves with adequatephosphate. The total soluble protein content of leaves decreasedwith phosphate deficiency in all three species; however, theleaf chlorophyll content was decreased only in sunflower andmaize and not in wheat. These results suggest that stomatalconductance did not restrict the CO₂ diffusion rate, ratherthe metabolism of the mesophyll was the limiting factor. Thisis shown by poor carboxylation efficiency and decreased apparentquantum yield for CO₂ assimilation, both of which contributedto the increase in relative mesophyll limitation of photosynthesisin phosphate deficient plants. Key words: Apparent quantum yield, carboxylation efficiency, phosphate nutrition, photosynthesis, stomatal and mesophyll limitation     

Long Term Effects of High CO2 Concentration on Photosynthesis of Water Hyacinth (Eichhornia crassipes (Mart.) Solms)

The photosynthetic response to CO₂ concentration, light intensityand temperature was investigated in water hyacinth plants (Eichhorniacrassipes (Mart.) Solms) grown in summer at ambient CO₂ or at10000 µmol(CO₂) mol^–1 and in winter at 6000 µmol(CO₂)mol^–1 Plants grown and measured at ambient CO₂ had highphotosynthetic rate (35 µmo1(CO₂) m^–2 s^–1),high saturating photon flux density (1500–2000) µmolm^–2 s^–1 and low sensitivity to temperature in therange 20–40 °C. Maximum photosynthetic rate (63 µmol(CO₂)m^–2 s^–1) was reached at an internal CO₂ concentrationof 800 µmol mol^–1. Plants grown at high CO₂ in summerhad photosynthetic capacities at ambient CO₂ which were 15%less than for plants grown at ambient CO₂, but maximum photosyntheticrates were similar. Photosynthesis by plants grown at high CO₂and high light intensity had typical response curves to internalCO₂ concentration with saturation at high CO₂, but for plantsgrown under high CO₂ and low light and plants grown under lowCO₂ and high light intensity photosynthetic rates decreasedsharply at internal CO₂ concentrations above 1000 µmol^–1. Key words: Photosynthesis, CO₂, enrichment, Eichhornia crassipes