Diurnal Pattern of Transpiration,Water Uptake and Water Budget of Succulents with Different CO2 Fixation Pathways

The water fluxes and the CO₂ exchange of three leaf succulents, Othonna opima, Cotyledon orbiculata and Senecio medley-woodii, with different leaf anatomy, growth form and CO₂ fixation pathways (C₃, CAM) were monitored with a gas exchange cuvette which was combined with a potometric system to quantify water uptake. Measurements, which are primarily valid for plants with a sufficient water supply, were made during 6 to 10 consecutive days under constant experimental conditions. Water uptake for 24 h exceeded water loss by transpiration only for a S, medley-woodii plant with 10 expanding but only 7 mature leaves. In this case the gained water evidently is put into leaf expansion. All other plants showed balanced transpiration and water uptake rates. O. opima and C. orbiculata have a similar life form, similar water storage volumes and the same natural habitat but their diurnal water uptake patterns differ significantly. In the C₃ plant O. opima water uptake increased when the transpiration increased or transpiration rates were higher than uptake rates and vice versa. On the contrary the CAM plant C. orbiculata transpired during the dark period at constant or decreasing rates but showed steadily increasing uptake rates. Senecio medley-woodii- and C. orbiculata are CAM plants with similar diurnal water uptake patterns with its maximum in uptake during or towards the end of the CO₂ dark fixation period. Water uptake of C. orbiculata was at its minimum at the end of the light period despite transpiration being maximal. The results were discussed considering the different CO₂ fixation pathways. In the investigated CAM succulents, C. orbiculata and S. medley-woodii, the CAM influenced water uptake throughout the whole day and not only during the CO₂ dark fixation period.     

冬小麦光合特征及叶绿素含量对保水剂和氮肥的响应

以不施保水剂和氮（N）肥为对照,测定了保水剂（60 kg·hm^-2）与不同N肥水平（0、225、450 kg·hm^-2）及其配施条件下大田小麦的光合特征、叶绿素含量和水分利用效率等指标,研究了冬小麦拔节期和灌浆期光合生理特征、叶绿素含量及水分利用对保水剂和N肥的响应.结果表明：灌浆期各处理的光合速率、气孔导度、胞间CO₂浓度、叶片水分利用效率及叶绿素含量均大于拔节期.在拔节期,单施N肥条件下,随施N量的增加,单叶水分利用效率提高,光合速率、气孔导度、胞间CO₂浓度及蒸腾速率均先增后减;225 kg·hm^-2 N肥处理的叶绿素含量最高.施用保水剂后,随施N量的增加,胞间CO₂浓度降低,而光合速率等均提高;单施保水剂及其与N肥配施提高了叶绿素含量,而过多N肥效果不显著在灌浆期,单施N肥显著提高了小麦的光合速率及水分利用效率,降低了气孔导度、胞间CO₂浓度及蒸腾速率;叶绿素含量随N肥用量的增加而增加.施用保水剂后,随N肥用量的增加,光合速率和叶片水分利用效率均先增后减,而胞间CO₂浓度和蒸腾速率先减后增,但均低于对照,气孔导度随施N量的增加而提高.单施保水剂的叶绿素含量显著提高,但其与N肥配施叶绿素含量有所降低.保水剂与N肥配合施用显著提高了小麦的千粒重、产量及水分生产效率.其中,保水剂与225 kg·hm^-2N肥配施处理的产量及水分生产效率均最高.     

Environmental control of crassulacean acid metabolism in Welwitschia mirabilis Hook. Fil. in its range of natural distribution in the Namib desert

Summary Within the area of its natural distribution in South West Africa, Welwitschia mirabilis has a less negative ¹³C value than C₃ plants and a more negative ¹³C value than C₄ species. This indicates that Welwitschia m. assimilates CO₂ partially via CAM when growing in its natural habitat. The difference between the ¹³C values of Welwitschia m. and of the C₃ species is significant in the savanna, whereas it is only small and statistically not significant in the grassland zone. The proportion of CO₂ fixed via CAM is largest in the coastal desert zone. There was no correlation between the ¹³C values and the Cl^- or ash content of the tissue. Thus, CAM in Welwitschia m. seems not to be induced by salt stress. There is no change in the ¹³C values along the persistent Welwitschia m. leaf. The present data indicate that on a broad geographical scale in the area of distribution temperature regime, and water stress as a modifying factor, determine CAM in Welwitschia m. The ecological implications are discussed by comparing the behaviour of Welwitschia m. with other CAM, C₃ and C₄ species of the accompanying flora.     

Regulation of Transpiration to Improve Crop Water Use

Decreasing fresh water supplies and increasing agricultural drought threaten sustainable worldwide crop production. Consequently, there is a global priority to develop crops with higher water use efficiency (WUE): biomass production or yield per unit of water used. Water use efficiency varies substantially among species and genotypes within a species, and a major effort is now underway to identify the genetic determinants of WUE. Today, it is known that genotypes in primary gene pools exhibit allelic variation for WUE through mechanisms that regulate transpiration, which is the conductance of water through stomata, the cuticle, and the boundary layer. Because of the differential diffusion properties of water and carbon dioxide (CO₂) through these pathways, it is feasible that WUE could be improved by decreasing transpiration without a concomitant reduction in CO₂ uptake. Since CO₂ uptake and transpirational water loss occur predominantly through stomatal pores, it is not surprising that genes involved in stomatal development and stomatal opening/closing impact WUE. Furthermore, loss- and gain-of-function genetic screens have identified genes that regulate transpiration and WUE by yet undetermined mechanisms. This review will discuss the genetic determinants that regulate transpiration and WUE in the context of the modern agricultural goal of improving WUE while sustaining biomass and yield.     

CO2 gas exchange and transpiration of Welwitschia mirabilis Hook. fil. in the central Namib desert

Summary The diurnal course of CO₂ gas exchange, ¹⁴CO₂ incorporation, malate and citrate content, and traspiration of Welwitschia mirabilis were measured in one of its natural habitats, the Welwitschia-Vlakte in the central Namib desert (Namibia), in order to decide which CO₂ fixation pathway is used by this gymnosperm.The CO₂ gas exchange of Welwitschia is that of a C₃ plant under arid conditions. Younger leaf parts show a two-peaked pattern of photosynthetic CO₂ uptake whereas in older parts the morning peak is followed by net CO₂ release during the rest of the day. The maximum rates of net photosynthesis decrease from 3.4 mol m^-2 s^-1 in 1-year-old parts to 1 mol m^-2 s^-1 in 7-year-old parts. No net CO₂ uptake was detected during the night. The diurnal CO₂ balance indicates that the old leaf parts live at the expense of the younger ones. Irrigation of Welwitschia plants resulted in an increased CO₂ uptake throughout the light period with maximum rate of 4.1 mol m^-2 s^-1. ¹⁴CO₂ was only incorporated during the day.The water loss of Welwitschia by transpiration is considerable, reaching a peak value of 1.9 mmol m^-2 s^-1 around noon. Leaf conductance corresponds with the twopeaked pattern of CO₂ uptake.Although there is no sign of a crassulacean acid metabolism in Welwitschia the leaf contains rather high amounts of malate (up to 200 mol g^-1 dry matter) and citrate (up to 250 mol g^-1 dry matter), which depend on leaf age but do not show any significant day-night oscillation.In spite of all this the ¹³C values are in the range of-17.77 to-19.64. Possible reasons for such a high ¹³C content in a C₃ plant are discussed.Dedicated to Prof. H. Walter, the pioneer of ecophysiological studies in the Namib desert     

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.     

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.     

Analysis of Stomatal and Nonstomatal Components in the Environmental Control of CO(2) Exchange in Leaves of Welwitschia mirabilis

In well-watered plants of Welwitschia mirabilis, grown in the glass-house under high irradiance conditions, net CO₂ assimilation was almost exclusively observed during the daytime. The plants exhibited a very low potential for Crassulacean acid metabolism, which usually resulted in reduced rates of net CO₂ loss for several hours during the night. In leaves exposed to the diurnal changes in temperature and humidity typical of the natural habitats, CO₂ assimilation rates in the light were markedly depressed under conditions resembling those occurring during midday, when leaf temperatures and the leaf-air vapor pressure differences were high (36°C and 50 millibars bar⁻¹, respectively). Studies on the relationship between CO₂ assimilation rate and intercellular CO₂ partial pressure at various temperatures and humidities showed that this decrease in CO₂ assimilation was largely due to stomatal closure. The increase in the limitation of photosynthesis by CO₂ diffusion, which is associated with the strong decline in stomatal conductance in Welwitschia exposed to midday conditions, may significantly contribute to the higher ¹³C content of Welwitschia compared to the majority of C₃ species.     

The Effect of Leaf Water Potential, Leaf Temperature and Light Intensity on Leaf Diffusion Resistance and the Transpiration of Leaves of Malus sylvestris

The relationship between leaf resistance to water vapour diffusion and each of the factors leaf water potential, light intensity and leaf temperature was determined for leaves on seedling apple trees (Malus sylvestris Mill. cv. Granny Smith) in the laboratory. Leaf cuticular resistance was also determined and transpiration was measured on attached leaves for a range of conditions. Leaf resistance was shown to be independent of water potential until potential fell below — 19 bars after which leaf resistance increased rapidly. Exposure of leaves to CO₂-free air extended the range for which resistance was independent of water potential to — 30 bars. The light requirement for minimum leaf resistance was 10 to 20 W m^?2 and at light intensities exceeding these, leaf resistance was unaffected by light intensity. Optimum leaf temperature for minimum diffusion resistance was 23 ± 2°C. The rate of change measured in leaf resistance in leaves given a sudden change in leaf temperature increased as the magnitude of the temperature change increased. For a sudden change of 1°C in leaf temperature, diffusion resistance changed at a rate of 0.01 s cm^?1 min^?1 whilst for a 9°C leaf temperature change, diffusion resistance changed at a rate of 0.1 s cm^?1 min^?1. Cuticular resistance of these leaves was 125 s cm^?1 which is very high compared with resistances for open stomata of 1.5 to 4 s cm^?1 and 30 to 35 s cm^?1 for stomata closed in the dark. Transpiration was measured in attached apple leaves enclosed in a leaf chamber and exposed to a range of conditions of leaf temperature and ambient water vapour density. Peak transpiration of approximately 5 × 10^?6 g cm^?2 s^?1 occurred at a vapour density gradient from the leaf to the air of 12 to 14 g m^?3 after which transpiration declined due presumably to increased stomatal resistance. Leaves in CO₂-free air attained a peak transpiration of 11 × 10^?6 g cm^?2 s^?1 due to lower values of leaf resistance in CO₂ free air. Transpiration then declined in these leaves due to development of an internal leaf resistance (of up to 2 s cm^?1). The internal resistance was masked in leaves at normal CO₂ concentrations by the increase in stomatal resistance.     

Photosynthesis,Transpiration, and Water Use Efficiency in Two Divergent Leymus Chinensis Populations from Northeast China

The net photosynthetic rate (P _N), transpiration rate (E), and water use efficiency (WUE) of two divergent Leymus chinensis populations from the grassland region of Northeast China were compared. The two populations experienced the similar habitats, but differed in leaf colour, stomata numbers, and chlorophyll contents. The leaf P _N for the grey-green (GG) population was greater than that for the yellow-green (YG) population, while the leaf E for GG population was lower than that for the YG population. The greater WUE for the GG population suggests that this type is more able to maintain higher P _N under drought and is more fit for the rangeland use in this climate region.     

Wind increases leaf water use efficiency

A widespread perception is that, with increasing wind speed, transpiration from plant leaves increases. However, evidence suggests that increasing wind speed enhances carbon dioxide (CO₂) uptake while reducing transpiration because of more efficient convective cooling (under high solar radiation loads). We provide theoretical and experimental evidence that leaf water use efficiency (WUE, carbon uptake per water transpired) commonly increases with increasing wind speed, thus improving plants' ability to conserve water during photosynthesis. Our leaf‐scale analysis suggests that the observed global decrease in near‐surface wind speeds could have reduced WUE at a magnitude similar to the increase in WUE attributed to global rise in atmospheric CO₂ concentrations. However, there is indication that the effect of long‐term trends in wind speed on leaf gas exchange may be compensated for by the concurrent reduction in mean leaf sizes. These unintuitive feedbacks between wind, leaf size and water use efficiency call for re‐evaluation of the role of wind in plant water relations and potential re‐interpretation of temporal and geographic trends in leaf sizes.     

The efficiency of water use in water stressed plants is increased due to ABA induced stomatal closure

Gas exchange and abscisic acid content of Digitalis lanata EHRH. have been examined at different levels of plant water stress. Net photosynthesis, transpiration and conductance of attached leaves declined rapidly at first, then more slowly following the withholding of irrigation. The intercellular partial pressure of CO₂ decreased slightly. The concentration of 2-cis(S)ABA increased about eight-fold in the leaves of non-irrigated plants as compared with well-watered controls. A close linear correlation was found between the ABA content of the leaves and their conductance on a leaf area basis. In contrast, the plot of net assimilation versus ABA concentration was curvilinear, leading to an increased efficiency of water use during stress. After rewatering, photosynthesis reached control values earlier than transpiration, leaf conductance and ABA content. From these data it is concluded that transpiration through the stomata is directly controlled by the ABA content, whereas net photosynthesis is influenced additionally by other factors.Possible reasons for the responses of photosynthesis and water use efficiency to different stress and ABA levels are discussed.Abbreviations A net CO₂ assimilation - ABA abscisic acid - C_i intercellular CO₂ concentration - g stomatal conductance - T transpiration - WUE water use efficiency     

Chloride as a macronutrient increases water‐use efficiency by anatomically driven reduced stomatal conductance and increased mesophyll diffusion to CO2

Chloride (Cl^?) has been recently described as a beneficial macronutrient, playing specific roles in promoting plant growth and water‐use efficiency (WUE). However, it is still unclear how Cl^? could be beneficial, especially in comparison with nitrate (NO₃^?), an essential source of nitrogen that shares with Cl^? similar physical and osmotic properties, as well as common transport mechanisms. In tobacco plants, macronutrient levels of Cl^? specifically reduce stomatal conductance (g_s) without a concomitant reduction in the net photosynthesis rate (A_N). As stomata‐mediated water loss through transpiration is inherent in the need of C₃ plants to capture CO₂, simultaneous increase in photosynthesis and WUE is of great relevance to achieve a sustainable increase in C₃ crop productivity. Our results showed that Cl^?‐mediated stimulation of larger leaf cells leads to a reduction in stomatal density, which in turn reduces g_s and water consumption. Conversely, Cl^? improves mesophyll diffusion conductance to CO₂ (g_m) and photosynthetic performance due to a higher surface area of chloroplasts exposed to the intercellular airspace of mesophyll cells, possibly as a consequence of the stimulation of chloroplast biogenesis. A key finding of this study is the simultaneous improvement of A_N and WUE due to macronutrient Cl^? nutrition. This work identifies relevant and specific functions in which Cl^? participates as a beneficial macronutrient for higher plants, uncovering a sustainable approach to improve crop yield.     

Arundo donax L. (Poaceae) — a C3 Species with Unusually High Photosynthetic Capacity

Gas exchange characteristics, chlorophyll a fluorescence and leaf water potential were investigated in the giant reed, Arundo donax, under natural conditions in an estuarine mangrove swamp in Durban, South Africa. Maximum photosynthetic CO₂ uptake ranged between 19.8 and 36.7 μmol m^?2 s^?1, depending on irradiance, and appeared to be regulated by leaf conductance. There was no saturation of CO₂ uptake or electron transport through PSII (ETR) with increasing irradiance up to 2500 μmol photons m^?2 s^?1. A linear relationship between CO₂ uptake, corrected for respiration (A), and ETR has only been reported for C₄ species and C₃ species when photorespiration is eliminated. From this relationship, it was calculated that 8.5 electrons were transported through PSII for the fixation of one mole of CO₂. Predawn leaf water potential was about ?0.5 MPa and decreased to ?1.5 MPa on a cloudy day and to ?2.1 MPa on a clear day. Diurnal change in leaf water potential had little influence on leaf conductance and hence CO₂ uptake. The molar water use efficiency (WUE) ranged between 4.1 and 9.3 μmol mmol^?1. Percentage photorespiration was between 36 and 39%.     

Changes in the Water Balance and Photosynthesis of Onion, Bean and Cotton Plants under Saline Conditions

The osmotic concentration (osmotic potential) of onion leaf sap did not adjust to chloride salinity, and consequently water potential, turgor, stomatal aperture and transpiration were reduced. Although osmotic concentration of bean and cotton leaf sap did adjust to a saline root medium and turgor was no less in the salinized plants than in the controls, stomata of the salinized plants remained only partly open and transpiration was reduced. Net photosynthesis of onion plants was reduced by salinity (this effect being much enhanced in a hot dry atmosphere) but it could be rapidly raised to the level of the controls by inducing elevated leaf turgor. Stomatal closure was initially responsible for most of the ～30 % reduction in photosynthesis of salinized beans. This was due to interference with CO₂ diffusion and could be overcome by raising the CO₂ concentration in the air. At a later stage of growth, salinity affected the light reaction of bean photosynthesis, and elevation of the air CO₂ had little effect. Closure of stomata of salinized cotton plants had only a relatively small effect on net photosynthesis. Light intensity and CO₂ concentration experiments showed that salinity was reducing the photosynthesis of cotton leaves mainly by affecting the light reaction of photosynthesis. It is concluded that chloride salinity does affect the water balance and rate of photosynthesis of plants and that the nature and degree of the effects will depend upon climatic conditions and may be very different between plant species and in the same species at different periods of growth.     

Differences in gas exchange contribute to habitat differentiation in Iberian columbines from contrasting light and water environments

During photosynthesis, respiration and transpiration, gas exchange occurs via the stomata and so plants face a trade‐off between maximising photosynthesis while minimising transpiration (expressed as water use efficiency, WUE). The ability to cope with this trade‐off and regulate photosynthetic rate and stomatal conductance may be related to niche differentiation between closely related species. The present study explored this as a possible mechanism for habitat differentiation in Iberian columbines. The roles of irradiance and water stress were assessed to determine niche differentiation among Iberian columbines via distinct gas exchange processes. Photosynthesis–irradiance curves (P–I curves) were obtained for four taxa, and common garden experiments were conducted to examine plant responses to water and irradiance stress, by measuring instantaneous gas exchange and plant performance. Gas exchange was also measured in ten individuals using two to four field populations per taxon. The taxa had different P–I curves and gas exchange in the field. At the species level, water stress and irradiance explained habitat differentiation. Within each species, a combination of irradiance and water stress explained the between‐subspecies habitat differentiation. Despite differences in stomatal conductance and CO₂ assimilation, taxa did not have different WUE under field conditions, which suggests that the environment equally modifies photosynthesis and transpiration. The P–I curves, gas exchange in the field and plant responses to experimental water and irradiance stresses support the hypothesis that habitat differentiation is associated with differences among taxa in tolerance to abiotic stress mediated by distinct gas exchange responses.     

Carbon dioxide assimilation and stomatal response of afroalpine giant rosette plants

Maximal rates of CO₂ assimilation of 8–11 mol m^-2 s^-1 at ambient CO₂ concentration were measured for Dendrosenecio keniodendron, D. brassica, Lobelia telekii and L. keniensis during the day in the natural habitat of these plants at 4,200 m elevation on Mt. Kenya. Even at these maximal rates, the CO₂ uptake of all species was found to correspond to the linear portion of the CO₂ response curve, with a calculated stomatal limitation for CO₂ diffusion of 42%. Photosynthesis was strongly reduced at temperatures above 15° C. In contrast to this sensitivity to high temperatures, frozen leaves regained full photosynthetic capacity immediately after thawing. Stomata responded to dry air, but not to low leaf water potentials which occurred in cold leaves and at high transpiration rates. During the day reduced rates of CO₂ uptake were associated with reduced light interception due to the erect posture of the rosette leaves and with high temperatures. Stomata closed at vapour pressure deficits which were comparable in magnitude to those characteristic of many lowland habitats (40 mPa Pa^-1).     

Changes in Transpiration, Net Carbon Dioxide Assimilation and Leaf Water Potential Resulting from Application of Hydrostatic Pressure to Roots of Intact Pepper Plants

Hydrostatic pressures varying from 0 to 6.0 bar were applied to roots of intact Capsicum annuum L. cv. California Wonder plants growing in nutrient solution and the rates of transpiration, and net CO₂ assimilation, apparent compensation point and leaf water potential measured. Increasing the pressure on the roots of plants with roots in solution with either -0.5 or -5.0 bar osmotic potential with 1 bar increments resulted in a decrease in transpiration. With the application of 1 or 2 bar pressure the rate of transpiration returned to near or above the original rate. An application of 3 or 4 bar pressure reduced the rate of transpiration of all plants. The transpiration of plants with roots in solution with -0.5 bar osmotic potential remained at the reduced rate for as long as these pressures were maintained. The transpiration of plants with roots in solution with -5.0 bar was only temporarily suppressed at these pressures. Changing the applied pressure from 3 or 4 bar to 0 resulted in a rapid increase in transpiration which lasted approximately 15 minutes. This was followed by a decrease in transpiration to a rate lower than before the pressure was applied. The pattern of response was similar for plants at low or high light intensity or at normal or low CO₂ concentrations. When leaf diffusive resistance was 6.0 s cm^?1 or greater, changes in net CO₂ assimilation were similar to those of transpiration. The apparent CO₂ compensation point increased as pressure was applied and decreased with a release in pressure. Leaf water potential increased with an increase in pressure and decreased with a decrease in pressure. The changes in leaf water potential were frequently but not always proportional to changes in pressure. It is postulated that the respouses noted were due to changes in resistance to flow of water from xylem terminals through the mesophyll cells and stomatal cavities to the atmosphere.     

Water use efficiency of two succulents with contrasting CO2 fixation pathways

Two succulents with similar growth forms but different types of photosynthesis, Cotyledon orbiculata (crassulacean acid metabolism, CAM) and Othonna opima (C₃ pathway), were investigated with respect to the modulation of water use efficiency (WUE) during the transition from the rainy season to subsequent drought. Environmental conditions were simulated in a controlled-environment experiment on the basis of data collected in the habitat of the two species in the southern Namib desert. Experiments included one or more periods of hot bergwind, which frequently occurs in this region. When water was readily available, daily net CO₂ fixation was similar in the two species. This result confirms that the daily CO₂ fixation of CAM plants is as high as that of morphologically similar C₃ plants adapted to the same habitat. As expected, both species reduced CO₂ fixation and water loss through transpiration during simulated hot bergwind periods and their WUE values increased. However, after the second hot bergwind period, nearly identical WUEs were recorded: 41.0 and 40.0 mmol mol^?1 for C. orbiculata and O. opima, respectively. Therefore the statement that a CAM plant is a better ‘water saver’ than a C₃ plant does not necessarily hold for CAM and C₃ plants with similar growth forms growing under the same environmental conditions.     

Interaction between elevated atmospheric concentration of CO2 and humidity on plant growth: comparison between cotton and radish

Cotton plants (Gossypium hirsutum L. var Deltapine 90) and radish plants (Raphanus sativus L var Round Red) were grown under full sunlight using a factorial combination of atmospheric CO₂ concentrations (350 µmol mol^-1 and 700 µmol mol^-1) and humidities (35% and 90% RH at 32 °C during the day). Cotton plants showed large responses to increased humidity and to doubled CO₂. In cotton plants, the enhanced dry matter yield due to doubled CO₂ concentration was 1.6-fold greater at low humidity than at high humidity. Apart from the direct effect of elevated CO₂ level on photosynthesis, the greater effect of doubled CO₂ concentration on dry matter yield at low humidity was probably due to: (1) increased leaf water potential caused by reduction of transpiration resulting from the negative CO₂ response of stomata to increased CO₂ concentration the consequence being greater leaf area expansion; (2) reduction of CO₂ assimilation rate at low humidity and normal CO₂ concentration as a result of humidity response of stomata causing reduction of intercellular CO₂ concentration. In contrast, apart from the very early stage of development, radish plants do not respond to increased humidity but had a relatively large response to doubled CO₂ concentration. Furthermore, due to the determinate growth pattern as well as having a prominent storage root, the extra photoassimilate derived at doubled CO₂ level is allocated to the storage root.Abbreviatios DAE day after emergence - LAD leaf areal density (leaf dry weight/leaf area) - LAR leaf area ratio (leaf area/plant dry weight) - NAR net assimilation rate - c_i internal CO₂ concentration - PPFD photosynthetic photon flux density - RGR relative growth rate - RLAGR relative leaf area growth rate - VPD vapour pressure deficit