Fusicoccin and Air Pollutant Injury to Plants : Evidence for Enhancement of SO(2) but Not O(3) Injury

Garden peas (Pisum sativum L. cv Alsweet) and a tomato mutant (Lycopersicon esculentum Mill. var flacca) were sprayed with fusicoccin, a fungal toxin affecting membrane transport properties, before exposure to SO₂ or O₃. Tomatoes treated with 10 micromolar fusicoccin and exposed to SO₂ (0.6 microliter per liter for 2 hours) exhibited twice as much foliar necrosis as untreated plants exposed to SO₂. Peas treated with fusicoccin and exposed to SO₂ (0.7 to 1.0 microliter per liter for 2 hours) exhibited 2 to 6 times more injury than untreated plants exposed to SO₂. Peas treated with fusicoccin and exposed to O₃ had less injury than untreated plants exposed to O₃ (0.1 to 0.3 microliter per liter for 2 hours). Several lines of evidence suggested that the fusicoccin enhancement of SO₂ injury is not the result of increased gas exchange, i.e. the tomato mutant has permanently open stomata under all conditions, and in peas fusicoccin had no effect on SO₂ or H₂O flux in plants exposed to 0.12 microliter per liter SO₂. However, a 21% greater leaf conductance in fusicoccin treated versus untreated plants indicated the possibility of some differences in gas exchange for peas exposed to 1.0 microliter per liter SO₂.     

Metabolic Basis for Injury to Plants from Combinations of O(3) and SO(2): Studies with Modifiers of Pollutant Toxicity

Pisum sativum L. cv Alsweet (garden pea) and Lycopersicon esculentum Mill. flacca (mutant tomato) were chosen to evaluate the metabolic basis for plant injury from combinations of O₃ + SO₂. The plants were exposed under conditions reported to specifically alter O₃ or SO₂ toxicity; light versus dark exposures, and treatment with the fungal metabolite fusicoccin (FC), the O₃ injury inhibitor N-[2-(2-oxo-1-imidazolidiny) ethyl]-N′-phenylurea (EDU), and the SO₂ injury stimulator diethyldithiocarbamate (DDTC). Plants were grown in controlled environment chambers and exposed to combinations of O₃ (0.05-0.2 microliters per liter) and SO₂ (0.1-0.3 microliters per liter) for 2 hours. Peas treated with FC had the same or greater injury (quantified by visual rating) with O₃ + SO₂ exposures compared to plants not treated with FC. For plants with open stomata in the dark as well as light, i.e. FC-treated peas and tomatoes, there was no change or an increase in foliar necrosis with O₃ + SO₂ exposures in the dark versus light. Peas treated with EDU had an almost complete absence of O₃ injury, no change in SO₂ injury, and moderate decreases in injury from combinations of O₃ + SO₂ compared to plants not treated with EDU. Tomatoes treated with DDTC showed the same or less injury compared to plants not treated with DDTC and exposed to O₃ or SO₂. The plant responses to the experimental treatments and O₃ + SO₂ resembled O₃ responses more than SO₂ responses. The evidence for O₃-like responses are: no change or increase in injury in the light versus dark, and EDU-induced decreases in injury. Evidences for SO₂-like responses are: incomplete protection from injury with EDU, and no change or increased injury to FC-treated versus untreated plants. Thus, a metabolic mechanism affected by both pollutants may be associated with the combination injury, e.g. effects the plasma membrane.     

Joint Action of O(3) and SO(2) in Modifying Plant Gas Exchange

The joint action of O₃ and SO₂ stress on plants was investigated by determining the quantitative relationship between air pollutant fluxes and effects on stomatal conductance. Gas exchange measurements of O₃, SO₂, and H₂O vapor were made for Pisum sativum L. (garden pea). Plants were grown under controlled environments, and O₃, SO₂, and H₂O vapor fluxes were evaluated with a whole-plant gas exchange chamber using the mass-balance approach. Maximum O₃ and SO₂ fluxes per unit area (2 sided) into leaves averaged 8 nanomoles per square meter per second with exposure to either O₃ or SO₂ at 0.1 microliters per liter. Internal fluxes of either O₃ or SO₂ were reduced by up to 50% during exposure to combined versus individual pollutants; the greatest reduction occurred with simultaneous versus sequential combinations of the pollutants. Stomatal conductance to H₂O was substantially altered by the pollutant exposures, with O₃ molecules twice as effective as SO₂ molecules in inducing stomatal closure. Stomatal conductance was related to the integrated dose of pollutants. The regression equations relating integrated dose to stomatal conductance were similar with O₃ alone, O₃ plus added SO₂, and O₃ plus SO₂ simultaneously; i.e. a dose of 100 micromoles per square meter produced a 39 to 45% reduction in conductance over nonexposed plants. With SO₂ alone, or SO₂ plus added O₃, a dose of 100 micromoles per square meter produced a 20 to 25% reduction in conductance. When O₃ was present at the start of the exposure, then stomatal response resembled that for O₃ more than the response for SO₂. This study indicated that stomatal responses with combinations of O₃ and SO₂ are not dependent solely on the integrated dose of pollutants, but suggests that a metabolic synergistic effect exists.     

Interspecific Variation in SO(2) Flux : Leaf Surface versus Internal Flux, and Components of Leaf Conductance

The objective of this study was to clarify the relationships among stomatal, residual, and epidermal conductances in determining the flux of SO₂ air pollution to leaves. Variations in leaf SO₂ and H₂O vapor fluxes were determined using four plant species: Pisum sativum L. (garden pea), Lycopersicon esculentum Mill. flacca (mutant of tomato), Geranium carolinianum L. (wild geranium), and Diplacus aurantiacus (Curtis) Jeps. (a native California shrub). Fluxes were measured using the mass-balance approach during exposure to 4.56 micromoles per cubic meter (0.11 microliters per liter) SO₂ for 2 hours in a controlled environmental chamber. Flux through adaxial and abaxial leaf surfaces with closed stomata ranged from 1.9 to 9.4 nanomoles per square meter per second for SO₂, and 0.3 to 1.3 millimoles per square meter per second for H₂O vapor. Flux of SO₂ into leaves through stomata ranged from ~0 to 8.5 (dark) and 3.8 to 16.0 (light) millimoles per square meter per second. Flux of H₂O vapor from leaves through stomata ranged from ~0 to 0.6 (dark) to 0.4 to 0.9 (light) millimole per square meter per second. Lycopersicon had internal flux rates for both SO₂ and H₂O vapor over twice as high as for the other species. Stomatal conductance based on H₂O vapor flux averaged from 0.07 to 0.13 mole per square meter per second among the four species. Internal conductance of SO₂ as calculated from SO₂ flux was from 0.04 mole per square meter per second lower to 0.06 mole per square meter per second higher than stomatal conductance. For Pisum, Geranium, and Diplacus stomatal conductance was the same or slightly higher than internal conductance, indicating that, in general, SO₂ flux could be predicted from stomatal conductance for H₂O vapor. However, for the Lycopersicon mutant, internal leaf conductance was much higher than stomatal conductance, indicating that factors inside leaves can play a significant role in determining SO₂ flux.     

Gas Exchange Characteristics of the Submerged Aquatic Crassulacean Acid Metabolism Plant, Isoetes howellii

The submerged aquatic plant Isoetes howellii Engelmann possesses Crassulacean acid metabolism (CAM) comparable to that known from terrestrial CAM plants. Infrared gas analysis of submerged leaves showed Isoetes was capable of net CO₂ uptake in both light and dark. CO₂ uptake rates were a function of CO₂ levels in the medium. At 2,500 microliters CO₂ per liter (gas phase, equivalent to 1.79 milligrams per liter aqueous phase), Isoetes leaves showed continuous uptake in both the light and dark. At this CO₂ level, photosynthetic rates were light saturated at about 10% full sunlight and were about 3-fold greater than dark CO₂ uptake rates. In the dark, CO₂ uptake rates were also a function of length of time in the night period. Measurements of dark CO₂ uptake showed that, at both 2,500 and 500 microliters CO₂ per liter, rates declined during the night period. At the higher CO₂ level, dark CO₂ uptake rates at 0600 h were 75% less than at 1800 h. At 500 microliters CO₂ per liter, net CO₂ uptake in the dark at 1800 h was replaced by net CO₂ evolution in the dark at 0600 h. At both CO₂ levels, the overnight decline in net CO₂ uptake was marked by periodic bursts of accelerated CO₂ uptake. CO₂ uptake in the light was similar at 1% and 21% O₂, and this held for leaves intact as well as leaves split longitudinally. Estimating the contribution of light versus dark CO₂ uptake to the total carbon gain is complicated by the diurnal flux in CO₂ availability under field conditions.     

Effects of SO(2) and O(3) on Allocation of C-Labeled Photosynthate in Phaseolus vulgaris

A series of laboratory exposures of two varieties of bush bean (Phaseolus vulgaris L., var 274 and var 290) was conducted to determine the sensitivity of [¹⁴C]photosynthate allocation patterns to alteration by SO₂ and O₃. Experiments with the pollution-resistant 274 variety demonstrated short-term changes in both ¹⁴C and biomass allocation to roots of ¹⁴CO₂-labeled plants but no significant effect on yield by up to 40 hours of exposure to SO₂ at 0.50 microliters per liter or 4 hours of O₃ at 0.40 microliters per liter. Subsequent experiments with the more sensitive 290 variety demonstrated significant alteration of photosynthesis, translocation, and partitioning of photosynthate between plant parts including developing pods. Significant increases in foliar retention of photosynthate (+40%) occurred after 8 hours of exposure to SO₂ at 0.75 microliters per liter (6.0 microliters per liter-hour) and 11 hours of exposure to O₃ at 0.30 microliters per liter-hour (3.3 microliters-hours). Time series sampling of labeled tissues after ¹⁴CO₂ uptake showed that the disruption of translocation patterns was persistent for at least 1 week after exposures ceased. Subsequent longer-term exposures at lower concentrations of both O₃ (0.0, 0.10, 0.15, and 0.20 microliters per liter) and SO₂ (0.0, 0.20, and 0.40 microliters per liter) demonstrated that O₃ more effectively altered allocation than SO₂, that primary leaves were generally more sensitive than trifoliates, and that responses of trifoliate leaves varied with plant growth stage. Altered rates of allocation of photosynthate by leaves were generally associated with alterations of similar magnitude and opposite direction in developing pods. Collectively, these experiments suggest that allocation patterns can provide sensitive indices of incipient growth responses of pollution-stressed vegetation.     

CO(2) and O(2) Exchange in Two Mosses, Hypnum cupressiforme and Dicranum scoparium

Photosynthetic CO₂ and O₂ exchange was studied in two moss species, Hypnum cupressiforme Hedw. and Dicranum scoparium Hedw. Most experiments were made during steady state of photosynthesis, using ¹⁸O₂ to trace O₂ uptake. In standard experimental conditions (photoperiod 12 h, 135 micromoles photons per square meter per second, 18°C, 330 microliters per liter CO₂, 21% O₂) the net photosynthetic rate was around 40 micromoles CO₂ per gram dry weight per hour in H. cupressiforme and 50 micromoles CO₂ per gram dry weight per hour in D. scoparium. The CO₂ compensation point lay between 45 and 55 microliters per liter CO₂ and the enhancement of net photosynthesis by 3% O₂versus 21% O₂ was 40 to 45%. The ratio of O₂ uptake to net photosynthesis was 0.8 to 0.9 irrespective of the light intensity. The response of net photosynthesis to CO₂ showed a high apparent K_m (CO₂) even in nonsaturating light. On the other hand, O₂ uptake in standard conditions was not far from saturation. It could be enhanced by only 25% by increasing the O₂ concentration (saturating level as low as 30% O₂), and by 65% by decreasing the CO₂ concentration to the compensation point. Although O₂ is a competitive inhibitor of CO₂ uptake it could not replace CO₂ completely as an electron acceptor, and electron flow, expressed as gross O₂ production, was inhibited by both high O₂ and low CO₂ levels. At high CO₂, O₂ uptake was 70% lower than the maximum at the CO₂ compensation point. The remaining activity (30%) can be attributed to dark respiration and the Mehler reaction.     

Stomatal Response and Leaf Injury of Pisum sativum L. with SO(2) and O(3) Exposures : I. INFLUENCE OF POLLUTANT LEVEL AND LEAF MATURITY

Plants of Pisum sativum L. `Alsweet' were grown under a controlled environment and exposed to SO₂ and O₃ to determine whether changes in stomatal aperture during exposure were related to subsequent leaf injury. Stomata consistently closed with injurious levels of SO₂ and O₃. Measurements with diffusion porometers demonstrated 75 and 25% lower conductance with SO₂ and O₃ exposures, respectively, compared to the conductance of control plants. Stomata also showed a closing response with noninjurious levels of SO₂ but an opening response with noninjurious levels of O₃. Stomata closed to the same degree with combinations of SO₂ plus O₃ as with SO₂ alone. Stomata of expanding leaves closed more during pollutant exposures than stomata of expanded leaves. The abaxial and adaxial stomata both exhibited closure with SO₂ and combinations of SO₂ plus O₃, but abaxial stomata tended to close and adaxial stomata tended to open with exposure to O₃ alone.     

Effects of CO(2) Enrichment and Carbohydrate Content on the Dark Respiration of Soybeans

During the period of most active leaf expansion, the foliar dark respiration rate of soybeans (Glycine max cv Williams), grown for 2 weeks in 1000 microliters CO₂ per liter air, was 1.45 milligrams CO₂ evolved per hour leaf density thickness, and this was twice the rate displayed by leaves of control plants (350 microliters CO₂ per liter air). There was a higher foliar nonstructural carbohydrate level (e.g. sucrose and starch) in the CO₂ enriched compared with CO₂ normal plants. For example, leaves of enriched plants displayed levels of nonstructural carbohydrate equivalent to 174 milligrams glucose per gram dry weight compared to the 84 milligrams glucose per gram dry weight found in control plant leaves. As the leaves of CO₂ enriched plants approached full expansion, both the foliar respiration rate and carbohydrate content of the CO₂ enriched leaves decreased until they were equivalent with those same parameters in the leaves of control plants. A strong positive correlation between respiration rate and carbohydrate content was seen in high CO₂ adapted plants, but not in the control plants.

Mitochondria, isolated simultaneously from the leaves of CO₂ enriched and control plants, showed no difference in NADH or malate-glutamate dependent O₂ uptake, and there were no observed differences in the specific activities of NAD⁺ linked isocitrate dehydrogenase and cytochrome c oxidase. Since the mitochondrial O₂ uptake and total enzyme activities were not greater in young enriched leaves, the increase in leaf respiration rate was not caused by metabolic adaptations in the leaf mitochondria as a response to long term CO₂ enrichment. It was concluded, that the higher respiration rate in the enriched plant's foliage was attributable, in part, to a higher carbohydrate status.

     

SO(2) Effect on Photosynthetic Activities of Intact Sugar Maple Leaves as Detected by Photoacoustic Spectroscopy

Short-term (4 hours) effect of different concentrations of SO₂ fumigation on in vivo photochemical activities of sugar maple (Acer saccharum Marsh.) leaves was investigated using photoacoustic spectroscopy. The relative quantum yield of O₂ evolution (ratio of O₂ signal to the photothermal signal) and photochemical energy storage are increased by 0.05 microliter per liter of SO₂. This increase is more pronounced in 5 to 7 year old saplings than in 3 month old seedlings. Both oxygen-relative quantum yield and energy storage of seedlings are inhibited by increased concentrations of SO₂ and the inhibition is concentration dependent. The inhibition is greater in seedlings than in saplings at 2 microliters per liter of SO₂, indicating the more susceptible nature of seedlings. The present study indicates a concentration dependent differential effect of SO₂ on photochemical activities of sugar maple leaves.     

Metabolic bases for differences in sensitivity of two pea cultivars to sulfur dioxide

An oxidative chain reaction of sulfite initiated by the superoxide ion produced in the Mehler reaction has been implicated in the damage of plants exposed to sulfur dioxide. The toxicity of SO₂ may be alleviated by free radical scavenging systems acting to terminate this chain reaction. Hence, the relative sensitivity of plants to SO₂ toxicity could depend on differences in the responses of the levels of antioxidant metabolites and enzymes. The effect of SO₂ exposure on glutathione and ascorbic acid contents, glutathione reductase, and superoxide dismutase activities was assayed in two cultivars (Progress, Nugget) of pea (Pisum sativum L.) in which apparent photosynthesis showed a differential sensitivity to 0.8 microliter per liter SO₂ (R. Alscher, J. L. Bower, W. Zipfel [1987] J Exp Bot 38:99-108). Total and reduced glutathione increased more rapidly and to a greater extent in the insensitive Progress than in the sensitive Nugget, as did glutathione reductase activities. Superoxide dismutase activities increased significantly in Progress, whereas no such change was observed in Nugget as a result of SO₂ exposure. This increase in superoxide dismutase activity was observed at 210 minutes after 0.8 microliter per liter SO₂ concentration had been reached, in marked contrast to the increases in reduced glutathione content and glutathione reductase activity, which were apparent at the 90 minute time point. These data suggest that one basis for the relative insensitivity of the apparent photosynthesis of the pea cultivar Progress to SO₂ is the enhanced response of glutathione reductase, superoxide dismutase activities, and glutathione content.     

C(4) Acid Metabolism and Dark CO(2) Fixation in a Submersed Aquatic Macrophyte (Hydrilla verticillata)

The CO₂ compensation point of the submersed aquatic macrophyte Hydrilla verticillata varied from high (above 50 microliters per liter) to low (10 to 25 microliters per liter) values, depending on the growth conditions. Plants from the lake in winter or after incubation in an 11 C/9-hour photoperiod had high values, whereas summer plants or those incubated in a 27 C/14-hour photoperiod had low values. The plants with low CO₂ compensation points exhibited dark ¹⁴CO₂ fixation rates that were up to 30% of the light fixation rates. This fixation reduced respiratory CO₂ loss, but did not result in a net uptake of CO₂ at night. The low compensation point plants also showed diurnal fluctuations in titratable acid, such as occur in Crassulacean acid metabolism plants. However, dark fixation and diurnal acid fluctuations were negligible in Hydrilla plants with high CO₂ compensation points.     

Ethylene and Ethane Production from Sulfur Dioxide-injured Plants

After alfalfa (Medicago sativa) seedlings were exposed to approximately 0.7 microliter per liter SO₂ for 8 hours, elevated ethylene and ethane production was observed. Ethylene production peaked about 6 hours and returned to control levels by about 24 hours following the fumigation, while ethane production peaked about 36 hours and was still above control levels 48 hours after the fumigation. Light had an opposite effect upon the production of the two gases: ethane production rates were higher from plants held in light, whereas ethylene production rates were higher from those held in the dark. Peak ethylene and ethane production rates from SO₂-treated plants were about 10 and 4 to 5 times greater, respectively, than those of the control plants. Ethylene appeared to be formed primarily from stressed yet viable leaves and ethane from visibly damaged leaves. The different time courses and light requirements for ethylene and ethane production suggest that these two gases were formed via different mechanisms. Light appears to have a dual role. It enhances SO₂-induced cellular damage and plays a role for repairs.     

Ethylene, Ethane, Acetaldehyde, and Ethanol Production By Plants under Stress

Red pine (Pinus resinosa Ait.) and paper birch (Betula papyrifera Marsh.) seedlings exposed to sulfur dioxide produced acetaldehyde and ethanol, and exhibited increased production of ethylene and ethane. Gas chromatographic measurement of head space gas from incubation tubes containing leaves or seedlings was a simple method of simultaneously measuring all four compounds. Increased ethylene production had two phases, a moderate increase from the beginning of the stress period and a large increase just prior to appearance of leaf lesions. Ethane production in SO₂-stressed plants did not increase until lesions appeared. Acetaldehyde and ethanol production began within 6 hours at 0.3 microliter per liter SO₂ and 24 hours at 0.1 microliter per liter SO₂ and continued throughout a 6-day fumigation. Production of acetaldehyde and ethanol continued when plants were removed to clean air for up to 2 days. A higher concentration of SO₂ (0.5 microliter per liter) induced acetaldehyde and ethanol production within 2 hours of the start of fumigation of birch and pine seedlings. A number of other stresses, including water deficit, freezing, and ozone exposure induced production of acetaldehyde and ethanol. Production of these compounds was not due to hypoxia, as the O₂ partial pressure in the incubation vessels did not decline. Increasing the O₂ partial pressure to 300 millimeters Hg did not affect production of these compounds. Production of ethylene, acetaldehyde, and ethanol declined when more than 80% of the leaf area became necrotic, while ethane production was linearly related to the percentage of necrosis. A number of woody and herbaceous plant species produced acetaldehyde and ethanol in response to freezing stress, while others did not. Measurement of these four compounds simultaneously in the gas phase may be a valuable method for monitoring plant stress, particularly air pollution stress.     

Stomatal Conductance and Sulfur Uptake of Five Clones of Populus tremuloides Exposed to Sulfur Dioxide

Plants of five clones of Populus tremuloides Michx. were exposed to 0, 0.2 or 0.5 microliter per liter SO₂ for 8 hours in controlled environment chambers. In the absence of the pollutant, two pollution-resistant clones maintained consistently lower daytime diffusive conductance (LDC) than did a highly susceptible clone or two moderately resistant clones. Differences in LDC among the latter three clones were not significant. At 0.2 microliter per liter SO₂, LDC decreased in the susceptible clone after 8 hours fumigation while the LDC of the other clones was not affected. Fumigation with 0.5 microliter per liter SO₂ decreased LDC of all five clones during the fumigation. Rates of recovery following fumigation varied with the clone, but the LDC of all clones had returned to control values by the beginning of the night following fumigation. Night LDC was higher in the susceptible clone than in the other clones. Fumigation for 16 hours (14 hours day + 2 hours night) with 0.4 microliter per liter SO₂ decreased night LDC by half. Sulfur uptake studies generally confirmed the results of the conductance measurements. The results show that stomatal conductance is important in determining relative susceptibility of the clones to pollution stress.     

Oxygen Uptake and Photosynthesis of the Red Macroalga, Chondrus crispus, in Seawater: Effects of Light and CO(2) Concentration

With an experimental system using mass spectrometry techniques and infra-red gas analysis of CO₂ developed for aquatic plants, we studied the responses to various light intensities and CO₂ concentrations of photosynthesis and O₂ uptake of the red macroalga Chondrus crispus S. The CO₂ exchange resistance at air-water interface which could limit the photosynthesis was experimentally measured. It allowed the calculation of the free dissolved CO₂ concentration. The response to light showed a small O₂ uptake (37% of net photosynthesis in standard conditions) compared to C₃ plants; it was always higher than dark respiration and probably included a photoindependent part. The response to CO₂ showed: (a) an O₂ uptake relatively insensitive to CO₂ concentration and not completely inhibited with high CO₂, (b) a general inhibition of gas exchanges below 130 microliters CO₂ per liter (gas phase), (c) an absence of an inverse relationship between O₂ and CO₂ uptakes, and (d) a low apparent K_m of photosynthesis for free CO₂ (1 micromolar). These results suggest that O₂ uptake in the light is the sum of different oxidation processes such as the glycolate pathway, the Mehler reaction, and mitochondrial respiration. The high affinity for CO₂ is discussed in relation to the use of HCO₃⁻ and/or the internal CO₂ accumulation.     

CO(2)-Enhanced Yield and Foliar Deformation among Tomato Genotypes in Elevated CO(2) Environments

Yield increases observed among eight genotypes of tomato (Lycopersicon esculentum Mill.) grown at ambient CO₂ (about 350) or 1000 microliters per liter CO₂ were not due to carbon exchange rate increases. Yield varied among genotypes while carbon exchange rate did not. Yield increases were due to a change in partitioning from root to fruit. Tomatoes grown with CO₂ enrichment exhibited nonepinastic foliar deformation similar to nutrient deficiency symptoms. Foliar deformation varied among genotypes, increased throughout the season, and became most severe at elevated CO₂. Foliar deformation was positively related to fruit yield. Foliage from the lower canopy was sampled throughout the growing season and analysed for starch, K, P, Ca, Mg, Fe, and Mn concentrations. Foliar K and Mn concentrations were the only elements correlated with deformation severity. Foliar K decreased while deformation increased. In another study, foliage of half the plants of one genotype received foliar applications of 7 millimolar KH₂PO₄. Untreated foliage showed significantly greater deformation than treated foliage. Reduced foliar K concentration may cause CO₂-enhanced foliar deformation. Reduced K may occur following decreased nutrient uptake resulting from reduced root mass due to the change in partitioning from root to fruit.     

The Effect of an Oxygen-free Atmosphere on Net Photosynthesis and Transpiration of Barley (Hordeum vulgare L.) and Wheat (Triticum aestivum L.) Leaves

Stomata of barley (Hordeum vulgare L.) and wheat (Triticum aestivum L.) leaves failed to open in the light and close in the dark or respond to changes in the CO₂ concentration of the atmosphere in either light or dark when the leaves were in an O₂-free atmosphere. In contrast, the expected responses to environmental changes were found in atmospheres containing 1.5% O₂. It appears that O₂ is necessary for both opening and closing of wheat and barley stomata.     

Foliar uptake of Cd by pea (Pisum sativum) and sugar beet (Beta vulgaris)

Pea ( Pisum sativum L. cv. Fenomen) and sugar beet ( Beta vulgaris L. cv. Monohill) were cultivated in nutrient media without or with 10 μM CdCl₂. Leaves of the same size and stage of development, detached or still attached to the intact plants, were submerged into redistilled water containing 1 to 250 μM CdCl₂. The uptake experiments were run for 1 to 8 h at pH 3.6 and 5.1. Cuticular transpiration rate, density of leaf and density of stomata were also measured. Percentage of open stomata was studied at different pH.
Foliar uptake of Cd into the leaf is evident since Cd is transported from the exposed part of the pea leaves, through the petioles and into the stipules, and since the Cd concentration of the leaves increases with time and external Cd concentration. The foliar uptake depends on the permeability of the cuticular membrane, which is increased by a high intrinsic Cd level, which in turn enhances the foliar uptake of Cd in sugar beet. Higher cuticular permeability in pea than in sugar beet is shown by a 2.5 times higher cuticular transpiration rate and a 4 times lower density of leaf for pea, which causes a 7 times higher foliar uptake in pea than in sugar beet. Low pH decreases the net uptake of Cd, probably by an exchange reaction in the cutin and pectin of the cuticular membrane. Stomata are not directly involved in the Cd uptake, and the differences in the sum total of stomatal aperture area per unit leaf area is not related to differences in foliar uptake of Cd. Percentage of open stomata, calculated as average of both sides of the leaves, was not affected by changes in pH: but especially at high pH. proportionally more stomata were open on the adaxial than on the abaxial side.     

Crassulacean acid metabolism (CAM) in an epiphytic ant-plant, Myrmecodia beccarii Hook.f. (Rubiaceae)

This study demonstrates unequivocally the presence of crassulacean acid metabolism (CAM) in a species of the Rubiaceae, the fourth largest angiosperm plant family. The tropical Australian endemic epiphytic ant-plant, Myrmecodia beccarii Hook.f., exhibits net CO₂ uptake in the dark and a concomitant accumulation of titratable acidity in plants in the field and in cultivation. Plants growing near Cardwell, in a north Queensland coastal seasonally dry forest of Melaleuca viridiflora Sol. ex Gaertn., accumulated ~50 % of their 24 h carbon gain in the dark during the warm wet season. During the transition from the wet season to the dry season, 24 h carbon gain was reduced whilst the proportion of carbon accumulated during the dark increased. By mid dry season many plants exhibited zero net carbon uptake over 24 h, but CO₂ uptake in the dark was observed in some plants following localised rainfall. In a shade-house experiment, droughted plants in which CO₂ uptake in the light was absent and dark CO₂ uptake was reduced, were able to return to relatively high rates of CO₂ uptake in the light and dark within 12 h of rewatering.