Restriction analysis and sequencing of the ITS regions and 5.8S gene of rDNA of Ganoderma isolates from infected oil palm and coconut stumps in Malaysia

Use of Crassulacean acid metabolism (CAM) plants in México and worldwide has a long history, but the morphological and photosynthetic aspects of these plants have only been considered recently. Emphasis in this article is on the daily net CO₂ uptake ability by three species of agaves and three species of cacti that are currently extensively cultivated in México for beverages, food, fodder, and forage ‐ Agave mapisaga, A. salmiana, A. tequilana, Opuntia ficus‐indica, O. robusta and Stenocereus queretaroensis. Data under controlled conditions are used to help interpret seasonal net CO₂ uptake patterns observed in the field. These CAM plants have instantaneous and total daily net CO₂ uptake values similar to those for highly productive C₃ and C₄ crops. The future increase in the cultivated area of CAM plants will have both agronomical and ecological ramifications because of the ability of these plants to endure prolonged drought and to sequester carbon during extended dry periods when few C₃ and C₄ crops and non‐CAM native plants can fix atmospheric CO₂.     

Responses of CAM species to increasing atmospheric CO2 concentrations

Crassulacean acid metabolism (CAM) species show an average increase in biomass productivity of 35% in response to a doubled atmospheric CO₂ concentration. Daily net CO₂ uptake is similarly enhanced, reflecting in part an increase in chlorenchyma thickness and accompanied by an even greater increase in water‐use efficiency. The responses of net CO₂ uptake in CAM species to increasing atmospheric CO₂ concentrations are similar to those for C₃ species and much greater than those for C₄ species. Increases in net daily CO₂ uptake by CAM plants under elevated atmospheric CO₂ concentrations reflect increases in both Rubisco‐mediated daytime CO₂ uptake and phosphoenolpyruvate carboxylase (PEPCase)‐mediated night‐time CO₂ uptake, the latter resulting in increased nocturnal malate accumulation. Chlorophyll contents and the activities of Rubisco and PEPCase decrease under elevated atmospheric CO₂, but the activated percentage for Rubisco increases and the K_M(HCO₃ ^? ) for PEPCase decreases, resulting in more efficient photosynthesis. Increases in root:shoot ratios and the formation of additional photosynthetic organs, together with increases in sucrose‐Pi synthase and starch synthase activity in these organs under elevated atmospheric CO₂ concentrations, decrease the potential feedback inhibition of photosynthesis. Longer‐term studies for several CAM species show no downward acclimatization of photosynthesis in response to elevated atmospheric CO₂ concentrations. With increasing temperature and drought duration, the percentage enhancement of daily net CO₂ uptake caused by elevated atmospheric CO₂ concentrations increases. Thus net CO₂ uptake, productivity, and the potential area for cultivation of CAM species will be enhanced by the increasing atmospheric CO₂ concentrations and the increasing temperatures associated with global climate change.     

Facultative CAM photosynthesis (crassulacean acid metabolism) in four species of <Emphasis Type="Italic">Calandrinia</Emphasis>, ephemeral succulents of arid Australia

Crassulacean acid metabolism (CAM) was demonstrated in four small endemic Australian terrestrial succulents from the genus Calandrinia (Montiaceae) viz. C. creethiae, C. pentavalvis, C. quadrivalvis and C. reticulata. CAM was substantiated by measurements of CO₂ gas-exchange and nocturnal acidification. In all species, the expression of CAM was overwhelmingly facultative in that nocturnal H⁺ accumulation was greatest in droughted plants and zero, or close to zero, in plants that were well-watered, including plants that had been droughted and were subsequently rewatered, i.e. the inducible component was proven to be reversible. Gas-exchange measurements complemented the determinations of acidity. In all species, net CO₂ uptake was restricted to the light in well-watered plants, and cessation of watering was followed by a progressive reduction of CO₂ uptake in the light and a reduction in nocturnal CO₂ efflux. In C. creethiae, C. pentavalvis and C. reticulata net CO₂ assimilation was eventually observed in the dark, whereas in C. quadrivalvis nocturnal CO₂ exchange approached the compensation point but did not transition to net CO₂ gain. Following rewatering, all species returned to their original well-watered CO₂ exchange pattern of net CO₂ uptake restricted solely to the light. In addition to facultative CAM, C. quadrivalvis and C. reticulata exhibited an extremely small constitutive CAM component as demonstrated by the nocturnal accumulation in well-watered plants of small amounts of acidity and by the curved pattern of the nocturnal course of CO₂ efflux. It is suggested that low-level CAM and facultative CAM are more common within the Australian succulent flora, and perhaps the world succulent flora, than has been previously assumed.     

Seasonal response to drought and rewatering in Portulacaria afra (L.) Jacq.

Summary Gas exchange characteristics of droughted and rewatered Portulacaria afra were studied during the seasonal shift from CAM to C₃ photosynthesis. ¹⁴CO₂ uptake, stomatal conductance, and total titratable acidity were determined for both irrigated and 2, 4, and 7.5 month waterstressed plants from summer 1984 to summer 1985. Irrigated P. afra plants were utilizing the CAM pathway throughout the summer and shifted to C₃ during the winter and spring. Beginning in September, P. afra plants shifted from CAM to CAM-idling after 2 months of water-stress. When water-stress was initiated later in the fall, exogenous CO₂ uptake was still measurable after 4 months of drought. After 7.5 months of stress, exogenous CO₂ uptake was absent. The shift from CAM to CAM-idling or C₃ in the fall and winter was related to when water stress was initiated and not to the duration of the stress. Gas exchange resumed within 24 h of rewatering regardless of the duration of the drought. In the winter and spring, rewatering resulted in a full resumption of daytime CO₂ uptake. Whereas during the summer, rewatering quickly resulted in early morning CO₂ uptake, but nocturnal CO₂ uptake through the CAM pathway was observed after 7 days. Gas exchange measurements, rewatering characteristics, and transpirational water loss support the hypothesis that the C₃ pathway was favored during the winter and spring. The CAM pathway was functional during the summer when potential for water loss was greater. Our investigations indicate that P. afra has a flexible photosynthetic system that can withstand long-term drought and has a rapid response to rewatering.     

The role of CAM in high rainfall cloud forests: an in situ comparison of photosynthetic pathways in Bromeliaceae

Crassulacean acid metabolism (CAM), an advanced photosynthetic pathway conferring water conservation to plants in arid habitats, has enigmatically been reported in some species restricted to extremely wet tropical forests. Of these, epiphytic Bromeliaceae may possess absorbent foliar trichomes that hinder gas‐exchange when wetted, imposing further limitations on carbon dioxide (CO₂) uptake. The hypothesis that the metabolic plasticity inherent to CAM confers an ecological advantage over conventional C₃ plants, when constant rainfall and mist might inhibit gas‐exchange was investigated. Gas‐exchange, fluorometry and organic acid and mineral nutrient contents were compared for the bromeliads Aechmea dactylina (CAM) and Werauhia capitata (C₃) in situ at the Cerro Jefe cloud forest, Panama (annual rainfall > 4 m). Daily carbon gain and photosynthetic nutrient use efficiencies were consistently higher for A. dactylina, due to a greater CO₂ uptake period, recycling of CO₂ from respiration and a dynamic response of CO₂ uptake to wetting of leaf surfaces. During the dry season CAM also had water conserving and photoprotective roles. A paucity of CAM species at Cerro Jefe suggests a recent radiation of this photosynthetic pathway into the wet cloud forest, with CAM extending diversity in form and function for epiphytes.     

Comparative ecophysiology of CAM and C3 bromeliads. III. Environmental influences on CO2 assimilation and transpiration

Abstract Field measurements of the gas exchange of epiphytic bromeliads were made during the dry season in Trinidad in order to compare carbon assimilation with water use in CAM and C₃ photosynthesis. The expression of CAM was found to be directly influenced by habitat and microclimate. The timing of nocturnal CO₂ uptake was restricted to the end of the dark period in plants found at drier habitats, and stomatal conductance in two CAM species was found to respond directly to humidity or temperature. Total night-time CO₂ uptake, when compared with malic-acid formation (measured as the dawn-dusk difference in acidity, ΔH⁺), could only account for 10–40% of the total ΔH⁺ accumulated. The remaining malic acid must have been derived from the refixation of respired CO₂ (recycling). Within the genus Aechmea (12 samples from four species), recycling was significantly correlated with night temperature at the six sample sites. Recycling was lowest in A. fendleri (54% of ΔH⁺ derived from respired CO₂), a CAM bromeliad with little water-storage parenchyma that is restricted to wetter, cooler regions of Trinidad. Gas-exchange rates of C₃ bromeliads were found to be similar to those of the CAM bromeliads, with CO₂ uptake from 1 to 3 μmol m^?2 s^?1 and stomatal conductances generally up to 100 mmol m^?2 s^?1. The midday depression of photosynthesis occurred in exposed habitats, although photosynthetically active radiation (PAR) limited photosynthesis in shaded habitats. CO₂ uptake of the C₃ bromeliad Guzmania lingulata was saturated at around 500 μmol m^?2 s^?1 PAR, suggesting that epiphytic plants found in the shaded forest understorey are shade-tolerant rather than shade-demanding. Transpiration ratios (TR) during CO₂ fixation in CAM (Phase I and IV) and C₃ bromeliads were compared at different sites in order to assess the efficiency of water utilization. For the epiphytes displaying marked uptake of CO₂, TR were found to be lower than many previously published values. In addition, the average TR values were very similar for dark CO₂ uptake in CAM (42 ± 41, n= 12), Phase IV of CAM (69 ± 36, n= 3) and for C₃ photosynthesis (99 ± 73, n= 4) in these plants. It appears that recycling of respired CO₂ by CAM bromeliads and efficient use of water in all phases of CO₂ uptake are physiological adaptations of bromeliads to arid microclimates in the humid tropics.     

Responses of succulents to plant water stress

Experiments were performed to test the hypothesis that succulents “shift” their method of photosynthetic metabolism in response to environmental change. Our data showed that there were at least three different responses of succulents to plant water status. When plant water status of Portulacaria afra (L.) Jacq. was lowered either by withholding water or by irrigating with 2% NaCl, a change from C₃-photosynthesis to Crassulacean acid metabolism (CAM) occurred. Fluctuation of titratable acidity and nocturnal CO₂ uptake was induced in the stressed plants. Stressed Peperomia obtusifolia A. Dietr. plants showed a change from C₃-photosynthesis to internal cycling of CO₂. Acid fluctuation commenced in response to stress but exogenous CO₂ uptake did not occur. Zygocactus truncatus Haworth plants showed a pattern of acid fluctuation and nocturnal CO₂ uptake typical of CAM even when well irrigated. The cacti converted from CAM to an internal CO₂ cycle similar to Peperomia when plants were water-stressed. Reverse phase gas exchange in succulents results in low water loss to carbon gain. Water is conserved and low levels of metabolic activity are maintained during drought periods by complete stomatal closure and continual fluctuation of organic acids.     

Seasonal Shifts of Photosynthesis in Portulacaria afra (L.) Jacq

Portulacaria afra (L.) Jacq., a perennial facultative Crassulacean acid metabolism (CAM) species, was studied under natural photoperiods and temperatures in San Diego, California. The plants were irrigated every fourth day throughout the study period. Measurements of ¹⁴CO₂ uptake, stomatal resistance, and titratable acidity were made periodically from July 1981 through May 1982. P. afra maintained C₃ photosynthesis during the winter and the spring. Diurnal acid fluctuations were low and maximal ¹⁴CO₂ uptake occurred during the day. The day/night ratio of carbon uptake varied from 5 to 10 and indicated little nocturnal CO₂ uptake. CAM photosynthesis occurred during the summer and a mixture of both C₃ and CAM during the fall. Large acid fluctuations of 100 to 200 microequivalents per gram fresh weight were observed and maximal ¹⁴CO₂ uptake shifted to the late night and early morning hours. Daytime stomatal closure was evident. A reduction in the day/night ratio of carbon uptake to 2 indicated a significant contribution of nocturnal CO₂ uptake to the overall carbon gain of the plant. The seasonal shift from C₃ to CAM was facilitated by increasing daytime temperature and accompanied by reduced daytime CO₂ uptake despite irrigation.     

Phosotynthesis in hemiepiphytic species of Clusia and Ficus

Summary Hemiepiphytic species in the genera Clusia and Ficus were investigated to study their mode of photosynthetic metabolism when growing under natural conditions. Despite growing sympatrically in many areas and having the same growth habit, some Clusia species show Crassulacean acid metabolism (CAM) whereas all species of Ficus investigated are C₃. This conclusion is based on diurnal CO₂ fixation patterns, diurnal stomatal conductances, diurnal titratable acidity fluctuations, and ¹³C isotope ratios. Clusia minor, growing in the savannas adjacent to Barinas, Venezuela, shows all aspects of Crassulacean acid metabolism (CAM) on the basis of nocturnal gas exchange, stomatal conductance, total titratable acidity, and carbon isotope composition when measured during the dry season (February 1986). During the wet season (June 1986), the plants shifted to C₃-type gas exchange with all CO₂ uptake occurring during the daylight hours. The carbon isotope composition of new growth was-28 to-29 typical of C₃ plants.     

Crassulacean acid metabolism in the epiphytic ferns Drymoglossum piloselloides and Pyrrosia longifolia: studies on responses to environmental signals

Abstract The paper reports the results of the comprehensive study of crassulacean acid metabolism in two epiphytic tropical ferns, Drymoglossum piloselloides and Pyrrosia longifolia. The plants were investigated under different light, temperature and water status. It was found that both species are obligate CAM plants. The diurnal acidity rhythm is due to the fluctuation in malic acid concentration, which accounts for the change in titratable acidity. Besides malic acid, shikimate and oxalate are found to be present, but not contributing to the CAM acid rhythm. The diurnal rhythm of malic acid content results in a corresponding rhythm in leaf water relations. Both Φ_Φ and Φ_total, were lowest at the end of the night, i.e. when the level of malic acid was highest. The effects of temperature on CO₂ exchange were inverse to those observed in other CAM plants. In both ferns studied, dark CO₂ fixation increased when the night temperature was increased. Increase in day temperature reduced CO₂ uptake during phase IV and during the following night. The observed responses of the ferns to temperature changes suggest that the in situ environmental conditions are optimal for their CAM performance. In weak light, the plants showed net CO₂ output during the midday deacidification period. Increases in light intensity reduced such CO₂ output. Under drought conditions, the CO₂ exchange in the ferns was reduced to zero within 5–6 d, indicating that the ferns studied are more susceptible to water deficiency than other CAM plants. This could be due to a higher cuticular conductance for water. The results are discussed, in particular, in relation to CAM performance of epiphytes growing in the wet tropics.     

Diurnal patterns of carbon dioxide,water vapour,and energy fluxes in pineapple [<Emphasis Type="Italic">Ananas comosus</Emphasis> (L.) Merr. cv. Red Spanish] field using eddy covariance

We analyzed the eddy covariance measurements of momentum, mass, and energy taken daily throughout five consecutive seasonal courses (i.e. 840 d after planting) of a pineapple [Ananas comosus (L.) Merr. cv. Red Spanish] field growing in the Orinoco lowlands. This field provides an opportunity for micrometeorological studies because of the flat and windy site; the seasonal weather including ENSO effects and the Crassulacean Acid Metabolism (CAM) physiology of the crop were additional attributes. Soil CO₂ flux was quantified and added to the net ecosystem exchange in order to obtain the canopy flux (F_C). The canopy CO₂ flux partially followed the four phases of CAM sensu Osmond (1978). The daily pattern of gaseous exchange in pineapple showed a continuum spectrum in which a major proportion of CO₂ uptake occurring during the daytime was common and in which the CAM expression was related to day and nocturnal CO₂ uptake. However, the benefits of CO₂ uptake at low water cost were constrained by the limited nocturnal CO₂ uptake. Seasonal and ontogenetic changes affected the energy exchange as well as the partitioning of available energy into sensible (Q_H) and latent (Q_LE) heat. When the hourly net radiation (Q_Rn) reached its maximum value, latent heat flux (Q_LE) to available energy throughout the vegetative and reproductive stages was 0.65, 0.05, 0.30, 0.11, and 0.33 for the 1997 wet season, 1997/98 dry season, 1998 wet season, 1998/99 dry season, and 1999 wet season, respectively. Throughout the growth period, we found the pivotal role of surface conductance (g _S) in both Q_LE and F_C. Furthermore, the canopy responded to environmental changes. During the wet seasons the g _S was strongly influenced by humidity mole fraction deficit and was usually lower than aerodynamic conductance, whereas during the dry seasons, soil water deficit limited evapotranspiration and production rates. For the fully canopy cover, the hourly trend of marginal water cost of pineapple carbon gain in the dry seasons indicated that g _S became sufficiently efficient to reduce the amount of water transported per unit of carbon gain. In the wet season, the coupling of CO₂ uptake and stomatal conductance was more effective in maintaining a higher proportionality between Q_LE and g _S.     

Crassulacean acid metabolism,CO2-recycling,and tissue desiccation in the Mexican epiphyte Tillandsia schiedeana Steud (Bromeliaceae)

After 23 days without water in a greenhouse, rates of nocturnal CO₂ uptake in Tillandsia schiedeana decreased substantially and maximum rates occurred later in the dark period eventually coinciding with the onset of illumination. Nocturnal CO₂ uptake accounted for less than half the total nighttime increase in acidity measured in well-watered plants. With increased tissue desiccation, only 11–12% of measured acid accumulation was attributable to atmospheric CO₂ uptake. Plants desiccated for 30 days regained initial levels of nocturnal acid accumulation and CO₂ uptake after rehydration for 10h. These results stress the importance of CO₂ recycling via CAM in this epiphytic bromeliad, especially during droughts.Partially supported by Biomedical Sciences Support Grant RR07037.     

Fluorescence Quenching in the Varied Photosynthetic Modes of Portulacaria afra (L.) Jacq

The kinetics of chlorophyll fluorescence were measured in Portulacaria afra (L.) Jacq. when the plants were functioning in either Crassulacean acid metabolism (CAM) or C₃/CAM cycling (called cycling) modes, as determined by fluctuation in titratable acidity and gas exchange properties. Cycling plants showed primarily daytime CO₂ uptake typical of C₃ plants, but with a slight diurnal acid fluctuation, whereas CAM plants showed nocturnal CO₂ uptake, daytime stomatal closure, and a large diurnal acid fluctuation. Results from fluorescence measurements indicated no significant differences in photochemical quenching between cycling and CAM plants; however, sizable differences were detected in nonphoto-chemical quenching (q_n), with the largest differences being observed during the middle of the day. Cycling plants had lower q_n than CAM plants, indicating altered photosynthetic regulation processes. This q_n difference was believed to be related to reduced internal CO₂ concentration in the CAM plants because of daytime stomatal closure and reduced deacidification rates in the late afternoon when most of the malic acid has been utilized. Experimentally, higher external CO₂ given to plants in the CAM mode resulted in a decline in q_n in comparison to that measured in plants in the cycling mode. No changes were observed in photochemical quenching when CO₂ was added.     

Leaf and Stem CO(2) Uptake in the Three Subfamilies of the Cactaceae

Net CO₂ uptake over 24-hour periods was examined for the leaves and for the stems of 11 species of cacti representing all three subfamilies. For Pereskia aculeata, Pereskia grandifolia, and Maihuenia poeppigii (subfamily Pereskioideae), all the net shoot CO₂ uptake was by the leaves and during the daytime. In contrast, for the leafless species Carnegiea gigantea, Ferocactus acanthodes, Coryphantha vivipara, and Mammillaria dioica (subfamily Cactoideae), all the shoot net CO₂ uptake was by the stems and at night. Similarly, for leafless Opuntia ficus-indica (subfamily Opuntioideae), all net CO₂ uptake occurred at night. For leafy members of the Opuntioideae (Pereskiopsis porteri, Quiabentia chacoensis, Austrocylindropuntia subulata), at least 88% of the shoot CO₂ uptake over 24 hours was by the leaves and some CO₂ uptake occurred at night. Leaves responded to the instantaneous level of photosynthetically active radiation (PAR) during the daytime, as occurs for C₃ plants, whereas nocturnal CO₂ uptake by stems of O. ficus-indica and F. acanthodes responded to the total daily PAR, as occurs for Crassulacean acid metabolism (CAM) plants. Thus, under the well-watered conditions employed, the Pereskioideae behaved as C₃ plants, the Cactoideae behaved as CAM plants, and the Opuntioideae exhibited characteristics of both pathways.     

Juvenile tank-bromeliads lacking tanks: do they engage in CAM photosynthesis?

In the epiphytic tillandsioids, Guzmania monostachia, Werauhia sanguinolenta, and Guzmania lingulata (Bromeliaceae), juvenile plants exhibit an atmospheric habit, whereas in adult plants the leaf bases overlap and form water-holding tanks. CO₂ gas-exchange measurements of the whole, intact plants and δ¹³C values of mature leaves demonstrated that C₃ photosynthesis was the principal pathway of CO₂ assimilation in juveniles and adults of all three species. Nonetheless, irrespective of plant size, all three species were able to display features of facultative CAM when exposed to drought stress. The capacity for CAM was the greatest in G. monostachia, allowing drought-stressed juvenile and adult plants to exhibit net CO₂ uptake at night. CAM expression was markedly lower in W. sanguinolenta, and minimal in G. lingulata. In both species, low-level CAM merely sufficed to reduce nocturnal respiratory net loss of CO₂. δ¹³C values were generally less negative in juveniles than in adult plants, probably indicating increased diffusional limitation of CO₂ uptake in juveniles.     

Physiological responses of Opuntia ficus-indica to growth temperature

The influences of various day/night air temperatures on net CO₂ uptake and nocturnal acid accumulation were determined for Opuntia ficus-indica, complementing previous studies on the water relations and responses to photosynthetically active radiation (PAR) for this widely cultivated cactus. As for other Crassulacean acid metabolism (CAM) plants, net nocturnal CO₂ uptake had a relatively low optimal temperature, ranging from 11°C for plants grown at day/night air temperatures of 10°C/0°C to 23°C at 45°C/35°C. Stomatal opening, which occurred essentially only at night and was measured by changes in water vapor conductance, progressively decreased as the measurement temperature was raised. The CO₂ residual conductance, which describes chlorenchyma properties, had a temperature optimum a few degrees higher than the optimum for net CO₂ uptake at all growth temperatures. Nocturnal CO₂ uptake and acid accumulation summed over the whole night were maximal for growth temperatures near 25°C/15°C, CO₂ uptake decreasing more rapidly than acid accumulation as the growth temperature was raised. At day/night air temperatures that led to substantial nocturnal acid accumulation (25°C/15°C.). 90% saturation of acid accumulation required a higher total daily PAR than at non-optimal growth temperatures (10°C/0°C and 35°C/25°C). Also, the optimal temperature of net CO₂ uptake shifted downward when the plants were under drought conditions at all three growth temperatures tested, possibly reflecting an increased fractional importance of respiration at the higher temperatures during drought. Thus, water status, ambient PAR, and growth temperatures must all be considered when predicting the temperature response of gas exchange for O. ficus-indica and presumably for other CAM plants.     

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.     

The effect of nitrogen availability and water conditions on competition between a facultative CAM plant and an invasive grass

Abstract Plants with crassulacean acid metabolism (CAM) are increasing their abundance in drylands worldwide. The drivers and mechanisms underlying the increased dominance of CAM plants and CAM expression (i.e., nocturnal carboxylation) in facultative CAM plants, however, remain poorly understood. We investigated how nutrient and water availability affected competition between Mesembryanthemum crystallinum (a model facultative CAM species) and the invasive C₃ grass Bromus mollis that co‐occur in California's coastal grasslands. Specifically we investigated the extent to which water stress, nutrients, and competition affect nocturnal carboxylation in M. crystallinum. High nutrient and low water conditions favored M. crystallinum over B. mollis, in contrast to high water conditions. While low water conditions induced nocturnal carboxylation in 9‐week‐old individuals of M. crystallinum, in these low water treatments, a 66% reduction in nutrient applied over the entire experiment did not further enhance nocturnal carboxylation. In high water conditions M. crystallinum both alone and in association with B. mollis did not perform nocturnal carboxylation, regardless of the nutrient levels. Thus, nocturnal carboxylation in M. crystallinum was restricted by strong competition with B. mollis in high water conditions. This study provides empirical evidence of the competitive advantage of facultative CAM plants over grasses in drought conditions and of the restricted ability of M. crystallinum to use their photosynthetic plasticity (i.e., ability to switch to CAM behavior) to compete with grasses in well‐watered conditions. We suggest that a high drought tolerance could explain the increased dominance of facultative CAM plants in a future environment with increased drought and nitrogen deposition, while the potential of facultative CAM plants such as M. crystallinum to expand to wet environments is expected to be limited.     

Crassulacean Acid Metabolism in the Succulent C(4) Dicot, Portulaca oleracea L Under Natural Environmental Conditions

Crassulacean acid metabolism (CAM) was examined under natural environmental conditions in the succulent C₄ dicot Portulaca oleracea L. Two groups of plants were monitored; one was watered daily (well watered), while the other received water once every 3 to 4 weeks to produce a ψ of −8 bars (drought stressed). Gas exchange, transpiration rate, and titratable acidity were measured for 24-hour periods during the growing season. CAM activity was greatest in drought-stressed plants during late August which had 13 hour days and day/night temperatures of 35/15°C. Under these conditions net CO₂ uptake occurred slowly throughout the night. Diurnal fluctuations of titratable acidity took place in both leaves and stems with amplitudes of 17 and 47 microequivalents per gram fresh weight, respectively. Transpiration data indicated greater opening of stomata during the night than the day. CAM was less pronounced in drought-stressed P. oleracea plants in July and September; neither dark CO₂ uptake nor positive carbon balance occurred during the July measurements. In contrast, well-watered plants appeared to rely on C₄ photosynthesis throughout the season, although some acid fluctuations occurred in stems of these plants during September.     

Comparative measurements of chlorophyll a fluorescence, acid accumulation and gas exchange in exposed and shaded plants of Clusia minor L. and Clusia multiflora H. B. K. in the field

 Changes in chlorophyll a fluorescence during the day and diurnal-changes of net CO₂-exchange and organic acid contents were determined in two species of the genus Clusia during the dry season in Venezuela. The investigations included plants of the C₃/CAM intermediate species Clusia minor and the C₃ species C. multiflora growing at exposed and shaded sites. Both species showed a C₃ pattern of net CO₂-exchange at the exposed site. In the shade under extreme drought stress C. minor showed a weak expression of CAM without CO₂-uptake during the afternoon (phase IV of CAM). C. multiflora growing in the shade exhibited a C₃-pattern of net CO₂-exchange and a small but significant nocturnal accumulation of citrate. Shaded plants of C. minor were able to double their light utilisation for electron transport and to reduce non-photochemical quenching during phase III compared to phase II of CAM. Furthermore, increase of electron transport rate through photosystem II in phase III of CAM is correlated to decarboxylation of malate. At the exposed site C. multiflora was less negatively affected by high PPFD than C. minor. This was shown by a lower reduction of potential electron quantum yield (F_v/F_m) and higher light utilisation of electron transport of C. multiflora compared to C. minor. At the exposed site C. minor did not make use of the CAM option to increase light utilisation of electron transport and to reduce non-photochemical quenching as did the plants growing in the shade. Received: 20 March 1996 / Accepted: 24 June 1996