Expression of P-Enolpyruvate Carboxylase and other Aspects of CAM during the Development of Peperomia camptotricha Leaves

During the development of Peperomia camptotricha leaves, metabolism changes from C₃-photosynthesis to Crassulacean acid metabolism (CAM). The youngest leaves showed no diurnal fluctuation of organic acids or P-enolpyruvate carboxylase (PEPc) activity. There was little evidence for PEPc protein using PEPc antibodies prepared from the CAM form of PEPc, nor was there evidence for PEPc mRNA when tested using a cDNA probe made from CAM P. scandens. As leaves matured, there was a parallel increase in titratable acidity, PEPc activity, PEPc protein, and PEPc mRNA. In leaf whorls 1 through 6, there was a significant linear correlation between the diurnal fluctuation of organic acids and PEPc activity indicating a functional relationship. The specific activity of PEPc increased as leaves matured and the K_m (PEP) decreased indicating that the enzyme was becoming more active. The ratio of PEPc protein to PEPc mRNA decreased as leaves matured. During the expression of CAM, the spongy mesophyll where most of the CAM activity occurs increased in thickness and per cent air space, whereas the palisade mesophyll where most of the C₃ activity occurs did not increase in size dramatically. The diurnal fluctuation of organic acids and the expression of PEPc activity, protein, and mRNA increased as the thickness of the spongy mesophyll increased. During the expression of CAM in Peperomia camptotricha, there appears to be coordinated expression of PEPc mRNA, protein, and activity, the commencement of diurnal organic acid fluctuation, and the development of the CAM-like spongy mesophyll. Thus the evidence suggests that CAM in this species is expressed during normal development and not in response to environmental signals.     

Mechanistic basis of differences in water-use efficiency between a CAM and a C3 species of Peperomia (Piperaceae)

Under ecologically realistic environmental conditions, the water-use efficiency (WUE) of Peperomia scandens , a CAM plant, was higher than that of the C₃ congener P. obtusifolia . This difference has been attributed to differences in stomatal activity between C₃ and CAM plants, coupled with differences in the evaporative demand of the atmosphere during which the stomata are open. This explanation has apparently not, however, been experimentally tested. Thus, WUEs were compared in these species in two experiments in which the atmospheric evaporative demand was identical (or nearly so) during the period of stomatal opening (i.e. during the night for the CAM plant and during the day for the C₃ species). In both experiments, the WUE of the CAM species was higher than that of the C₃ species. These results suggest that factors other than differences in atmospheric environmental conditions must also be responsible for the observed differences in WUE. Because CO₂ uptake rates of the CAM species were substantially lower than those of the C₃ species, the lower WUE in the CAM species resulted primarily from lower transpiration rates. Lower rates of water loss in P. scandens , relative to rates in P. obtusifolia , were ascribed, in part, to lower stomatal densities. Thus, leaf morphological differences, in addition to differences in atmospheric evaporative demand, help to explain the high WUE typically measured in CAM plants.     

Photosynthetic flexibility and ecophysiological plasticity: questions and lessons from Clusia, the only CAM tree, in the neotropics

The discovery of crassulacean acid metabolism (CAM) in the trees of Clusia: arrival in the limelight of international research 8 II. Phylogeny 8 III. Photosynthetic physiotypes 10 IV. Metabolic flexibility: organic acid variations 12 V. The environmental control of photosynthetic flexibility 13 VI. Phenotypic plasticity: physiotypes and morphotypes 16 VII. Ecological amplitude and habitat impact 16 VIII. Conclusions and outlook 21 Acknowledgements 22 References 22 Summary It is the aim of this review to present a monographic survey of the neotropical genus Clusia on scaling levels from molecular phylogeny, metabolism, photosynthesis and autecological environmental responses to ecological amplitude and synecological habitat impact. Clusia is the only dicotyledonous genus with real trees performing crassulacean acid metabolism (CAM). By way of introduction, a brief historical reminiscence describes the discovery of CAM in Clusia and the consequent increase in interest in studying this particular genus of tropical shrubs and trees. The molecular phylogeny of CAM in the genus is compared with that in Kalancho? and the Bromeliaceae. At the level of metabolism and photosynthesis, the great plasticity of expression of photosynthetic physiotypes, i.e. (i) C(3) photosynthesis, (ii) CAM including CAM idling, (iii) CAM cycling and (iv) C(3)/CAM-intermediate behaviour, as well as metabolic flexibility in Clusia is illustrated. At the level of autecology, the factors water, irradiance and temperature, which control photosynthetic flexibility, are assessed. The phenotypic plasticity of physiotypes and morphotypes is described. At the level of synecology, the ecological amplitude of Clusia in the tropics and the relations to habitat are surveyed.     

Transformation of a CAM plant, the facultative halophyte Mesembryanthemum crystallinum by Agrobacterium tumefaciens

This study is the first to demonstrate that a foreign DNA can be delivered into cells of facultative halophyte crassulacean acid metabolism (CAM) plant, Mesembryanthemum crystallinum L. with Agrobacterium tumefaciens. This plant can be induced to change from C3 to CAM by drought and various stresses, and is a good model to study the environment stress on metabolism not only at whole plant but also at cell level. The β-glucuronidase (GUS) and kanamycin (Km) resistance genes were introduced into this plant. The average successful rate of transformation was about 54.5% with root tissue or 53.0% with hypocotyl tissue. Based on the resistance to Km, polymerase chain reaction (PCR) detection and GUS expression, transformation with Agrobacterium tumefaciens was successful for introducing foreign genes into M. crystallinum. This revised version was published online in June 2006 with corrections to the Cover Date.     

PPiase-Activated ATP-Dependent H+ Transport at the Tonoplast of Mesophyll Cells of the CAM Plant Kalanchoë daigremontiana*

The co-ordinated action of the two proton-transporting enzymes at the tonoplast of the CAM plants. daigremontiana, viz. the ATPase and the PP_iase, was studied by measuring fluorescent dye quenching. The initial rates of ATP and PP_i-dependent H⁺ transport into tonoplast vesicles were additive, i.e. the sum of the rates obtained with each substrate alone was in the range obtained with both substrates added together at the same time. Conversely, the activities of the two H⁺ pumps were non-additive in establishing the steady-state level, indicating that the final steady state was under thermodynamic control of a maximal attainable proton gradient. The initial rates of ATP-dependent H⁺ transport were stimulated enormously if ATP was added a few minutes after pre-energization of the vesicles with PP_i. This stimulation was observed only when the PP_iase was active. A similar effect was not found for PP_i-dependent H⁺ transport after pre-energization with ATP. Hence, a PP_iase-activated ATP-dependent H⁺ transport can be distinguished from the basic ATP- and the basic PP_i-dependent H⁺ transport. In parallel a PP_i-dependent stimulation of ATP hydrolysis in the absence of ionophores was measured, which can only be attributed to the activity of the PP_iase. PP_iase-activated ATP-dependent H⁺ transport depends on the presence of permeant anions. It shows properties of both H⁺ transport activities, i.e. the chloride and malate stimulation and the DCCD inhibition of the ATP-dependent H⁺ transport activity, the nitrate stimulation and the KF inhibition of the PP_i-dependent H⁺ transport activity. Only MgPP_i and MgATP were effective as the respective substrates. The PP_iase-activated ATP-dependent H⁺ transport had a half life of about 5–9 minutes. It is concluded that the PP_iase may play an important role in kinetic regulation of the ATPase, and implications for CAM metabolism are discussed.     

Comparative ecophysiology of CAM and C3 bromeliads. II. Field measurements of gas exchange of CAM bromeliads in the humid tropics

Abstract The results described represent the first detailed measurements of gas exchange of epiphytic plants with crassulacean acid metabolism (CAM) in the humid tropics. A portable steady-state CO₂ and H₂O porometer was used to measure net exchange rates of CO₂ and H₂O vapour (J_CO2, J_H2O), leaf temperature (T₁), air temperature (T_A), air relative humidity (RH) and photosynthetically active radiation (PAR) for bromeliads in the field during the dry season in February and March 1983 on the tropical island of Trinidad. Different lengths of tubing (up to 25 m) were used so that the gas exchange could be measured of bromeliads in situ in their epiphytic habitats. Derived parameters such as leaf-air water-vapour-concentration difference (Δ_w), water-vapour conductance of leaves (g) and internal CO₂ partial pressure (pⁱ_CO2) could be calculated. The particular problems of making such measurements in the humid tropics due to high relative humidities and high dew-point temperatures are discussed. The long and often broad, strap-like leaves of bromeliads are well suited for measurements with the steady-state porometer. It is shown that CAM activity varies along the length of individual leaves, and variability between different leaves is also demonstrated. The major phases of CAM, i.e. nocturnal stomalal opening, CO₂ uptake and dark fixation as malic acid (Phase I), daytime stomatal closure and light-dependent assimilation of CO₂ derived from decarboxylation of the malic acid (Phase III), and late-afternoon stomatal opening with direct light-dependent assimilation of atmospheric CO₂ (Phase IV) were all clearly shown by CAM bromeliads in situ. Their expression and magnitude depended on the environmental conditions. An early-morning peak of CO₂ uptake as is characteristic of Phase II of CAM was not detected during the night-day transition. A bromeliad intermediate between C₃ and CAM, Guzmania monostachia, showed substantial net CO₂ uptake in the early morning but no net uptake integrated over the whole of the night.     

Root distribution and seasonal production in the northwestern Sonoran Desert for a C3 subshrub, a C4 bunchgrass, and a CAM leaf succulent

To investigate root distribution with depth, which can affect competition for water, surface areas of young and old roots were determined in 4-cm-thick soil layers for the C3 subshrub Encelia farinosa Torrey and A. Gray, the C4 bunchgrass Pleuraphis rigida Thurber, and the CAM (crassulacean acid metabolism) leaf succulent Agave deserti Engelm. At a site in the northwestern Sonoran Desert these codominant perennials had mean rooting depths of only 9-10 cm for isolated plants. Young roots had mean depths of 5-6 cm after a winter wet period, but 11-13 cm after a summer wet period. Young roots were most profuse in the winter for E. farinosa, which has the lowest optimum temperature for root growth, and in the summer for P. rigida, which has the highest optimum temperature. Roots for interspecific pairs in close proximity averaged 2-3 cm shallower for A. deserti and a similar distance deeper for the other two species compared with isolated plants, suggesting partial spatial separation of their root niches when the plants are in a competitive situation. For plants with a similar root surface area, the twofold greater leaf area and twofold higher maximal transpiration rate of E. farinosa were consistent with its higher root hydraulic conductivity, leading to a fourfold higher estimated maximal water uptake rate than for P. rigida. Continuous water uptake accounted for the shoot water loss by A. deserti, which has a high shoot water-storage capacity. A lower minimum leaf water potential for P. rigida than for A. deserti indicates greater ability to extract water from a drying soil, suggesting that temporal niche separation for water uptake also occurs.     

Oxygen isotope composition of CAM and C3 Clusia species: non-steady-state dynamics control leaf water 18O enrichment in succulent leaves

Leaf gas exchange and leaf water (18)O enrichment (Delta(18)O(L)) were measured in three Clusia species under field conditions during dry and wet seasons and in Miconia argentea during the dry season in the Republic of Panama. During the dry season, all three Clusia species used crassulacean acid metabolism (CAM); during the wet season Clusia pratensis operated in the C(3) mode, while Clusia uvitana and Clusia rosea used CAM. Large departures from isotopic steady state were observed in daytime Delta(18)O(L) of the Clusia species, especially during the dry season. In contrast, daytime Delta(18)O(L) was near isotopic steady state in the C(3) tree M. argentea. Across the full data set, non-steady-state predictions explained 49% of variation in observed Delta(18)O(L), whereas steady-state predictions explained only 14%. During the wet season, when Delta(18)O(L) could be compared with Clusia individuals operating in both C(3) and CAM modes, steady-state and non-steady-state models gave contrasting predictions with respect to interspecific variation in daytime Delta(18)O(L). The observed Delta(18)O(L) pattern matched that predicted for the non-steady state. The results provided a clear example of how non-steady-state control of leaf water (18)O dynamics can shift the slope of the relationship between transpiration rate and daytime Delta(18)O(L) from negative to positive.     

Comparative ecophysiology of CAM and C3 bromeliads. IV. Plant water relations

Abstract An investigation was carried out into the water relations of CAM and C₃ bromeliads in their natural habitat during the dry season in Trinidad. Measurements were made of xylem tension with the pressure chamber and of cell-sap osmotic pressure and titratable acidity on crushed leaf samples. A steady-state CO₂ and H₂O-vapour porometer was also used so that changes in leaf water relations during individual day-night cycles could be directly related to gas-exchange patterns in situ. Xylem tension changed in parallel with transpiration rate and in general reached its maximum value in CAM bromeliads at night and in C₃ bromeliads during the day. In addition, large nocturnal increases in cell-sap osmotic pressure and titratable acidity (ΔH⁺) typically occurred in the CAM bromeliads. The C₃-CAM intermediate Guzmania monostachia showed slight nocturnal acidification, but had higher values of xylem tension during the day. Very high values of AH+ were observed in the CAM species when the tanks of the epiphytic bromeliads contained water: Aechmea nudicaulis showed a mean maximum ΔH⁺ of 474 mol m^?3, the highest value so far observed for CAM plants. On some nights dew formed on the leaf surfaces of the epiphytes, partially curtailing gas exchange and leading to a marked decrease in xylem tension in both C₃ and CAM species. Between-site comparisons were also made for a wide range of habitats from arid coastal scrub to montane rain forest. Compared with values characteristic of other life-forms, xylem tension and cell-sap osmotic pressure were low for all bromeliads, and did not differ significantly in co-occurring CAM and C₃ bromeliads. Mean maximum xylem tension (10 species in total) ranged from 0.29 M Pa at the montane sites to 0.67 MPa at the most arid site, and mean minimum osmotic pressure (17 species) from 0.51 to 0.97 MPa. At the arid sites the bromeliads were exclusively CAM species, two of which (Aechmea aquilega and Bromelia plumieri) grew terrestrially in the undergrowth of the coastal scrub. Xylem tension in these species was low enough to indicate that they must be functionally independent of the substratum during the dry season. In the wetter part of Trinidad, no between-site differences in leaf water relations were found along an altitudinal gradient in the Northern Mountain Range; seasonal differences in this area were also small. Overall, leaf water relations and gas exchange in the bromeliads were strongly affected both by short-term changes in water availability and by longer-term climatic differences in the various regions of the island.     

One Morphotype, Three Physiotypes: Sympatric Species of Clusia with Obligate C3 Photosynthesis, Obligate CAM and C3-CAM Intermediate Behaviour

Abstract: Among about 150 species of the genus of Clusia, morphologically very similar neotropical shrubs and trees, 20 have been studied ecophysiologically and 39 original publications were screened here for key data on the potential performance of the various species. I have collected data on carbon isotope discrimination (8⁷³C), day-night oscilliations of malate (Amal), citrate (Acitr) and titratable protons (AH), maximum rates of net CO₂ exchange in the dark (Dark J_co2) and in the light (Light J_co2) apparent rate of photosynthetic electron transport at PS II (ETR), effective quantum yield of non-cyclic electron transport at PS II (AF/F'_m) at 1000 umol m-² s-¹ PPFD, and potential quantum yield of PS II of leaves adapted to short periods of darkness at midday (F_v/F_m midday) and after relaxation overnight (F_v/F_m predawn). The 20 species can be arranged from predominant C₃ photosynthesis to principally CAM. There may be only a few bona fide obligatory CAM species in the genus, but it is doubtful if there are obligatory C₃ species. The data were then used to provide comparisons of intrinsic capabilities for Clusia species occurring sympatrically at two sites each, in Brazil and Venezuela. No clear advantage of CAM emerges from these comparisons under the stress of high insolation and low water availability at these sites. Different Clusia species are successful in different ways and with different intrinsic ecophysiological capacities. The conventional expectations in CAM as a drought and light stress adaptation are confounded in Clusia to the extent that on some occasions C₃ photosynthesis seems to be the superior strategy. However, it appears, that C₃/CAM plasticity which is so widespread in the genus, with many species and potentially rapid speciation, allows a particularly wide ecological amplitude.     

Competing carboxylases: circadian and metabolic regulation of Rubisco in C3 and CAM Mesembryanthemum crystallinum L

The temporal co-ordination of ribulose 1·5-bisphosphate carboxylase/oxygenase (Rubisco) and phosphoenolpyruvate carboxylase (PEPc) activities by Mesembryanthemum crystallinum L. in C(3) and crassulacean acid metabolism (CAM) modes was investigated under conventional light-dark (LD) and continuous light (LL) conditions. When C(3) , net CO(2) assimilation rate increased during each subjective night under LL with maximum carboxylation unrelated to Rubisco activation state. The CAM circadian rhythm of CO(2) uptake was more pronounced, with CO(2) assimilation rate maximal towards the end of each subjective night. In vivo and in vitro techniques were integrated to map carboxylase enzyme regulation to the framework provided by CAM LL gas exchange activity. Rubisco was activated in vitro throughout each subjective dark period and consistently deactivated at each subjective dawn, similar to that observed at true dawn in constitutive CAM species. Instantaneous carbon isotope discrimination showed in vivo carboxylase co-dominance during the CAM subjective night, initially by Rubisco and latterly C(4) (PEPc), despite both enzymes seemingly activated in vitro. The circadian rhythm in titratable acidity accumulation was progressively damped over successive subjective nights, but maintenance of PEPc carboxylation capacity ensures that CAM plants do not become progressively more 'C(3) -like' with time under LL.     

Estimation of Photorespiration Rate by Simultaneous Measurements of CO2, Gas Exchange Rate,and Chlorophyll Fluorescence Quenching in the C3 Plant Vigna Radiata (L.) Wilczek and the C4 Plant Amaranthus Mongostanus L.

So far the photorespiration rate (R _P) in a leaf has been determined as the difference between the net photosynthetic rates (P _N) measured in 21 % O₂ air (P _N21%) and 3 % O₂ air (P _N3%). In the C₃ plant Vigna radiata and the C₄ plant Amaranthus mongostanus L., P _N and chlorophyll fluorescence quenching in leaves were monitored simultaneously. R _P of leaves in situ was estimated as termed R _PE from the electron transport rates through photosystem 2 (PS2), and compared with R _PO (P _N3% – P _N21%). In V. radiata R _PO was 11.9 µmol(CO₂) m^–2 s^–1 and the ratio of R _PO to P _N21% was 42.2 %, whereas the ratio of R _PE to P _N21% was 25.7 %. This suggests that R _PO may be over-estimated for the real R _P in normal air. In A. mongostanus, P _N was almost not changed with a decrease in O₂ concentration from 21 to 3 %, whereas the quantum yield of PS2 was evidently affected by the change in O₂ concentration. This fact shows the presence of photorespiration in this C₄ species, where R _PE was equivalent to 3.8 % of P _N21%.     

Comparative Study of the C3/CAM Intermediate Species Clusia parviflora Saldanha et Engi. and the Obligate CAM Species Clusia hilariana Schlecht. Growing Sympatrically Exposed and Shaded in the Coastal Restinga of Brazil

Abstract: The C₃/CAM intermediate species, C/usia parviflora Saldanha et EngI., and the obligate CAM species Clusia hilariana Schlecht., occur sympatrically in the coastal sand dune vegetation of the Restinga of Brazil. Their photosynthetic activity at an exposed and at a shaded site was compared by measuring gas exchange (porometry), chlorophyll a fluorescence parameters, organic acid levels (malic and citric) and carbon isotope ratios. At the shaded site, low photosynthetic photon flux densities (PPFD) strongly restricted photosynthetic activity. However, C parviflora could readily make use of light flecks. At the exposed site, C. parviflora was much less affected by photoinhibition than C. hilariana . The CAM species showed higher apparent rates of linear photosynthetic electron transport (ETR) and higher effective quantum yield of PSII (ΔF/F'_m) than did C. parviflora during high insolation in the middle of the day, i.e., the time of Phase Ill of CAM. Nevertheless, it suffered much more severe acute photoinhibition that was not reversible after 20 min of darkening during this time, and even some chronic photoinhibition not reversible overnight. Comparative studies of sympatric physiotypes with different modes of photosynthesis of a given leaf morphotype, as available in the genus Cksia , challenge some CAM dogmas, e.g., CAM may not always be superior at exposed sites and may not always provide better photoprotection at high PPFD. However, the idea that C₃/CAM plasticity allows occupation of a wider range of habitats is supported.     

Comparative ecophysiology of CAM and C3 bromeliads. I. The ecology of the Bromeliaceae in Trinidad

Abstract This article deals with the physiological ecology of the Bromeliaceae, a large neotropical family containing both terrestrial and epiphytic forms, as well as many species with crassulacean acid metabolism (CAM). The article is in two parts. In the first, we review what is known of the occurrence of CAM and C₃ species in the Bromeliaceae. The photosynthetic pathways are discussed in the context of the major taxonomic divisions within the family and the great diversity of bromeliad life-forms. Of the three subfamilies, the Pitcairnioideae contain both C₃ and CAM species and are essentially all terrestrial. In contrast, the Tillandsioideae are entirely epiphytic or saxicolous, with CAM species being restricted to the genus Tillandsia, And in the Bromelioideae all species show CAM, but terrestrial and epiphytic forms are found in about equal numbers. The evidence suggests that both CAM and the epiphytic habit arose more than once in the family's evolutionary history. In the second part we consider the photosynthetic ecology of the various bromeliad life-forms in more detail using the specific example of Trinidad (West Indies). CAM bromeliads tend to be centred on the drier regions of the island and C₃ forms on the wetter areas. However, at any one site there is a marked vertical stratification of species within the forest profile. Based on the known habitat preferences of the bromeliads, six contrasting sites were selected for field studies in Trinidad. These ranged from arid coastal scrub to montane rain forest, the vegetational and climatic characteristics of which are described here. The constancy of δ¹³C values (carbon-isotope ratios) for individual CAM species in these markedly different habitats emphasized the need for ecophysiological studies to characterize environmental effects on CO₂ assimilation and transpiration. The following papers in this series present the results of a comparative investigation of gas exchange and leaf water relations of CAM and C₃ bromeliads in situ at the various sites.     

Carbon-Isotope Ratios and Photosynthetic Pathways in the Neotropical Family Rapateaceae

Abstract: The Rapateaceae is a small, mainly Neotropical family of terrestrial or occasionally epiphytic herbs that grow on mesic, nutrient-poor sites. Some recent studies suggest that the Rapateaceae may be closely related to the Bromeliaceae, one of the major families containing CAM plants. To investigate the photosynthetic pathway in Rapateaceae, the plant carbon-isotope ratio (δ¹³C) was determined for samples from dried herbarium specimens for 85 of the approximately 100 species in the family. The δ¹³C values ranged from - 37.7 to - 19.8 ‰. Most Rapateaceae showed δ¹³C values typical of C₃ plants. However, six species ( Kunhardtia rhodantha Maguire, Marahuacaea schomburgkii (Maguire) Maguire, Saxofridericia compressa Maguire, Stegolepis grandis Maguire, St. guianensis Klotzsch ex Körn. and St. squarrosa Maguire) showed δ¹³C values less negative than - 23 ‰, i.e., at the higher end of the range for C₃ plants and at the lower end of the distribution for plants exhibiting CAM. The δ¹³C values became significantly less negative with increasing altitude (regression analysis indicating a change from about - 30.7 ‰ at sea level to - 22.5 ‰ at 2500 m). Although other environmental factors and the type of tissue analysed may also influence δ¹³C values, these results suggest that some Rapateaceae may be capable of performing CAM. Further studies, including measurements of diel gas exchange patterns and leaf organic-acid fluctuations, would be needed to demonstrate CAM in Rapateaceae unequivocally, but living material of many of these enigmatic plants is difficult to obtain.     

Carbon Flow and Metabolic Specialization in the Tissue Layers of the Crassulacean Acid Metabolism Plant, Peperomia camptotricha

Leaves of Peperomia camptotricha contain three distinct upper tissue layers and a one-cell thick lower epidermis. Light and dark CO₂ fixation rates and the activity of ribulose bisphosphate carboxylase/oxygenase and several C₄ enzymes were determined in the three distinct tissue layers. The majority of the C₄ enzyme activity and dark CO₂ fixation was associated with the spongy mesophyll, including the lower epidermis; and the least activity was found in the median palisade mesophyll. In contrast, the majority of the C₃ activity, that is ribulose bisphosphate carboxylase/oxygenase and light CO₂ fixation, was located in the palisade mesophyll. In addition, the diurnal flux in titratable acidity was greatest in the spongy mesophyll and lowest in the palisade mesophyll. The spatial separation of the C₃ and C₄ phases of carbon fixation in P. camptotricha suggests that this Crassulacean acid metabolism plant may have low photorespiratory rates when it exhibits daytime gas exchange (that is, when it is well watered). The results also indicate that this plant may be on an evolutionary path between a true Crassulacean acid metabolism plant and a true C₄ plant.     

Comparison of Photosynthetic Responses of the Sympatric Tropical C3 Species Clusia multiflora H. B. K. and the C3-CAM Intermediate Species Clusia minor L. to Irradiance and Drought Stress in a Phytotron1

Abstract: Clusia multiflora H. B. K., an obligate C₃ species and Clusia minor L. a C₃/CAM intermediate species, are two physio-types of a similar morphotype. They can sympatrically occupy secondary savanna sites exposed to high insolation in the tropics. In C. multiflora severe stress, i.e., switching shade-grown plants to high light plus drought, resulted in leaves browning or yellowing and becoming necrotic. However, in long-term light stress C. multiflora was able to grow new leaves with their photosynthetic apparatus fit for high light conditions. Shade-grown C. minor readily overcame switching to high light conditions and drought, responding by a rapid change from C₃ photosynthesis to CAM. Decreasing _soil led to increased abscisic acid levels in the leaves of C. minor, however CAM induction was not directly related to this and was mainly determined by increased PPFD. Both species were capable of rapid accumulation of zea-xanthin for acute photoprotection following high PPFD exposure. The maximum capacity for zeaxanthin accumulation was larger in C. minor, but under steady high PPFD it only partially made use of this capacity, relying on high internal CO₂ concentrations of Phase Ill of CAM, in addition to zeaxanthin, for acute photo-protection. Thus, by different means the two species perform well under high light conditions. However, C. multiflora needs time for development of adapted leaves under such stress conditions while the more flexible C. minor can readily switch from low light to high light conditions.     

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.