Phosphoenolpyruvate carboxylase genes in C3, crassulacean acid metabolism (CAM) and C3/CAM intermediate species of the genus Clusia: rapid reversible C3/CAM switches are based on the C3 housekeeping gene

The genus Clusia includes species that exhibit either the C3 or crassulacean acid metabolism (CAM) mode of photosynthesis, or those that are able to switch between both modes according to water availability. In order to screen for species-specific genetic variability, we investigated the key carboxylase for CAM, phosphoenolpyruvate carboxylase (PEPC). Sequence analysis of DNA isolated from the obligate CAM species, Clusia hilariana, the obligate C3 species, Clusia multiflora, and an intermediate species that can switch between C3 and CAM photosynthesis, Clusia minor, revealed three different isoforms for C. hilariana and one each for the other two species. Sequence alignments indicated that PEPC from the intermediate species had high homology with the C3 protein and with one of CAM plant proteins. These were assumed to constitute 'housekeeping' proteins, which can also support CAM in intermediate species. The other two isoforms of the CAM plant C. hilariana were either CAM-specific or showed homologies with PEPC from roots. Phylogenetic trees derived from neighbour-joining analysis of amino acid sequences from 13 different Clusia species resulted in two distinct groups of plants with either 'housekeeping' PEPC only, or additionally CAM-related isoforms. Only C. hilariana showed the third, probably root-specific isoform. The high homology of the PEPC from the intermediate species with the C3 protein indicates that for the reversible transition from the C3 to CAM mode of photosynthesis, the C3 type of PEPC is sufficient. Its expression, however, is strongly increased under CAM-inducing conditions. The use of the C3 isoform could have facilitated the evolution of CAM within the genus, which occurred independently for several times.     

The Genus Clusia L.: Molecular Evidence for Independent Evolution of Photosynthetic Flexibility

Abstract: Members of the Clusiaceae genus Clusia (tropical trees and shrubs) belong to the small group of dicotyledonous trees which are able to perform crassulacean acid metabolism (CAM). Most of the species are able to switch between C₃ and CAM modes of photosynthesis and only a few are restricted to either C₃ or CAM. In order to discover possible phylogenetic relationships with regard to the mode of photosynthesis, we investigated 17 species of the genus Clusia, and one species each of the Clusiaceae genera Oedematopus and Hypericum on the basis of internal transcribed spacer (ITS) sequences between the 18S and 26S coding regions of nuclear ribosomal DNA. Little length variation was detected in the ITS region of Clusia species. ITS1 sequences ranged from 255 to 260 bp and ITS2 sequences from 208 to 210 bp. Neighbour-joining and parsimony analyses of these sequences resulted in considerable differences in cluster formation when compared to a classification based on morphological characteristics. The molecular data also give no indication of a group-specific evolution of modes of photosynthesis, i.e., C₃ and CAM. We thus conclude that CAM has evolved independently several times within the genus Clusia.     

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.     

石斛属植物光合碳同化途径地理分异研究进展

系统总结了我国石斛属植物光合作用现状,结合石斛属植物光合作用碳同化途径研究,概括了兼性景天酸代谢植物的碳同化路径特征,分析了景天酸代谢表达程度与生态环境的关系,进而归纳出石斛属植物在光合作用碳同化途径方面存在地理分异。最后指出了石斛属植物系统发育研究领域存在的问题,提出从系统发育视角,采用分子系统学技术来研究石斛属植物光合碳同化途径地理分异的生物学机制。     

Clusia: Holy Grail and enigma

Clusia is the only genus with bona fide dicotyledonous trees performing Crassulacean acid metabolism (CAM). Clusia minor L. is extraordinarily flexible, being C(3)/CAM intermediate and expressing the photosynthetic modes C(3), CAM, CAM-cycling, and CAM-idling. C(3) photosynthesis and CAM can be observed simultaneously in two opposite leaves on a node and possibly even within the same leaf in the interveinal lamina and the major vein tissue, respectively. The relative activity of photosystem II (PhiPSII) indicating photosynthetic energy use, is larger under photorespiratory than under non-photorespiratory conditions due to the particular energy demand of photorespiration. The heterogeneity of PhiPSII over the leaves as visualized by chlorophyll fluorescence imaging in the C(3) mode is larger under non-photorespiratory conditions than under photorespiratory conditions. These observations indicate that photorespiration, presumably by its particular energy demand, synchronizes photosynthetic activity over the leaves. In the CAM mode, the heterogeneity of PhiPSII is more dependent on the transitions between CAM phases. Free-running circadian oscillations of photosynthesis are strongly dampened in both the C(3) and the CAM mode. Photorespiration is under circadian clock control in both the C(3) and the CAM mode. PhiPSII and the heterogeneity of PhiPSII oscillate in phase with CO(2) uptake and photorespiration only under non-photorespiratory conditions. Under photorespiratory conditions, PhiPSII does not oscillate and there is no heterogeneity, again indicating the stabilizing function of photorespiration. Plants acclimatized to perform CAM switch to C(3) photosynthesis during free-running oscillations while subjected to constant illumination.     

Implications of Genotypic Diversity and Phenotypic Plasticity in the Ecophysiological Success of CAM Plants,Examined by Studies on the Vegetation of Madagascar1

Abstract: On the basis of δ¹³C‐values, genotypic diversity and phenotypic plasticity of CAM behaviour in plants of the Malagasy vegetation is surveyed. The study compares CAM patterns performed in the wild on the levels of genera (Kalanchoë [Crassulaceae], Angraecum [Orchidaceae], Lissochilus [Orchidaceae] and Rhipsalis [Cactaceae]), on the level of a family (Didiereaceae) and finally on the level of a common growth form, namely in leafless orchids. For Rhipsalis, also non‐Malagasy species were included in the comparison. The genus Kalanchoë was found to be dominated by species representing the CAM‐physiotype with CO₂ fixation taking place only during the night, whereas the CAM/C3‐ and the C3‐physiotypes (with limited intrinsic CAM potential) were less frequent. The opposite holds true for Angraecum. In the genus Rhipsalis, in the Didiereacean family and in the leafless orchids only the CAM‐physiotype is represented. The photosynthetic physiotypes of CAM plants were found to be related to the environmental conditions of the habitat. That is, strong CAM performers are typically abundant in the dry climatic zones or at otherwise dry niches, species of the C3‐physiotype (possibly with weak intrinsic capability of CAM performance) are distributed at humid sites and those of the CAM/C3‐physiotype occupy sites with medium and changing exposure to stress. Phenotypic plasticity of CAM, as indicated by the intraspecific variability of the δ¹³C‐values, was lower in the CAM‐physiotype compared with the CAM/C3‐physiotype. Our data support the view that strong stress leads to the dominance of highly adapted specialists among the CAM plants, with low phenotypic plasticity of the photosynthetic behaviour, whereas medium stress advances the unfolding of plastic CAM behaviour. Moreover, the data suggest that genera comprising all three physiotypes (Kalanchoë, Angraecum) are dispersed all over Madagascar, whilst groups comprising only strong CAM performers are restricted to limited areas or special types of habitats. This suggests that both genotypic diversity and phenotypic plasticity are important factors for the ecophysiological success of CAM.     

The evolutionary relationship between stomatal mechanism, crassulacean acid metabolism and C4 photosynthesis

Abstract. All of the features of crassulacean acid metabolism (CAM) and most characteristics of C₄ photosynthesis are exhibited by stomatal guard cells. It is proposed that CAM and possibly also C₄ photosynthesis result from the expression in photosynthetic cells of genetic information which is expressed only in guard cells of C₃ plants.     

Ecophysiological studies on orchids of Madagascar: incidence and plasticity of crassulacean acid metabolism in species of the genus Angraecum Bory

The present study is an investigation on photosynthetic options in an orchid taxon and deals with the mainly epiphytes comprising genus Angraecum Bory. The incidence of crassulacean acid metabolism (CAM) in Angraecum species collected at various habitats in Madagascar was surveyed by analysis of stable carbon isotope composition (¹³C values). The values showed both inter- and intraspecific variability and suggest that in situ about 50% of the analysed species perform C3 photosynthesis, 20% moderate CAM (fixation of external CO₂ during day-and night-time) and 30% pronounced CAM (CO₂ uptake entirely during the night). The photosynthetic behaviour of the species indicated by the ¹³C values was clearly related to the habitat from where the samples derived. In A. eburneum, A. sororium and particularly in A. sesquipedale the stable carbon isotope analysis was complemented by measurements of CAM performance under controlled conditions. The experiments with A. sesquipedale revealed that drought and temperature are important factors modulating CAM, whereas variation of the leaf-to-air water vapor pressure difference was less effective. Altogether, the results of the study support the view that the high biological adaptability and thus the ecological success of the genus Angraecum is largely based on genotypic diversity and intraspecific plasticity of the photosynthetic behaviour.     

Seasonal variation in crassulacean acid metabolism by the aquatic isoetid Littorella uniflora

The seasonal temperature acclimation in crassulacean acid metabolism (CAM) and photosynthetic performance were investigated in the aquatic isoetid, Littorella uniflora. Plants were collected monthly from January to September, and CAM capacity and photosynthesis rates were measured at 5, 10, 15, and 20?°C. Seasonal acclimation was observed for CAM (Q (10) range: 0.6-1.8), and CAM was optimised close to ambient temperature throughout the season. Thus, in winter acclimated L. uniflora, the short-term response to raised temperature resulted in a decline in CAM capacity. Even though the ambient CAM increased from winter to spring/summer, CAM was present in cold acclimated plants, thus indicating an ecophysiological role for CAM even in winter. Similar to CAM, seasonal acclimation was observed in the light and carbon-saturated photosynthesis (Q (10) values ranged from 1.4 to 2.3), and the photosynthetic capacity was generally higher during the winter at all temperatures, indicating compensatory investments in the photosynthetic apparatus. Thus, L. uniflora displayed seasonal temperature acclimation with respect to both CAM and photosynthesis. The estimated in situ contribution of CAM to the carbon budget in L. uniflora was independent of season and varied from 23 to 46?%. A positive correlation between photosynthetic capacity and CAM capacity (both measured in the lab at temperature close to ambient temperature) was found, and the ratio of CAM activity to photosynthetic capacity was higher in summer compared with winter plants. Overall, the results from the present study support the suggested role of CAM as a carbon conserving mechanism of importance for survival in a carbon-limited habitat.     

Expression of Modes of Photosynthesis (C3, CAM) in Clusia criuva Camb. in a CerradolGallery Forest Transect

Abstract: The large majority of the Ca . 150 species of the neotropical shrub and tree genus Clusia have the potential to perform Crassulacean acid metabolism (CAM). They are either obligate CAM plants or C₃/CAM intermediate plants. Only a very small percentage of the plants studied so far are apparently obligate C₃ species. Among these was C. criuva , until recent laboratory studies showed that it may also have a certain CAM capacity under artificial stress conditions. Measurements of stomatal conductance (porometry) and chlorophyll fluorescence variables of C. criuva occurring along a transect from deep shade inside a gallery forest across the semi-shaded ecotone towards a cerrado and into the exposed cerrado itself in central Brazil now show that it can adapt its photosynthetic apparatus to effective performance of C₃ photosynthesis under highly different photosynthetic photon flux densities. In addition, however, it does have a certain potential for CAM and cannot be considered as a strictly obligate C₃ plant. Should a basic capacity for performing CAM be a general property of the genus, the quest for CAM traits in other remaining putatively obligate C₃ species of the genus ought to be pursued.     

Comparison of the performance of three different ecophysiological life forms in a sandy coastal restinga ecosystem of SE-Brazil: a nodulated N2-fixing C3-shrub (Andira legalis (Vell.) Toledo), a CAM-shrub (Clusia hilariana Schltdl.) and a tap root C3-hemicryptophyte (Allagoptera arenaria (Gomes) O. Ktze.)

In a sandy coastal restinga ecosystem NE of Rio de Janeiro, Brazil, subject to environmental stress due to high irradiance, high temperature and low water supply, a comparative ecophysiological study of three species of different morphotypes and physiotypes was conducted during the dry season. The morphotypes were two shrubs, Clusia hilariana Schltdl. and Andira legalis (Vell.) Toledo, and the taproot hemicryptophyte Allagoptera arenaria (Gomes) O. Ktze. The physiotype differences were that C. hilariana was performing crassulacean acid metabolism (CAM), A. legalis was a nodulated N₂ fixing legume and A. arenaria had ample access to water by ground water tapping roots. All three species were light stressed and showed photoinhibition and high maximum values of non-photochemical quenching of chlorophyll fluorescence. δ¹³C values of bulk leaf organic matter (which integrate over the life span of the leaf) and instantaneous gas exchange patterns demonstrated that C. hilariana was performing CAM and the other two species C₃-photosynthesis. A. arenaria performed generous and A. legalis conserving use of water. Based on the CO₂ concentrating mechanism of CAM C. hilariana had the highest maximum rates of apparent photosynthetic electron transport, ETR_max. Uptake of atmospheric CO₂ in the afternoon (phase IV of CAM) was expressed weakly showing that the plants were under some but not severe water stress. A. legalis showed the highest levels of total N and soluble non-protein N-compounds in its organs due to N₂ fixation which, however, did not confer a higher photosynthetic capacity that must have been limited by factors other than nitrogen supply. Accumulation of amino compounds like proline and γ-aminobutyric acid in leaves of A. legalis which are known to act as osmoprotectants is likely to indicate drought stress in the dry season. Maximum net CO₂ uptake of photosynthesis was higher in the water spending A. arenaria than in A. legalis. The comparative analysis of physiological traits characterised either instantaneously or integrated over the longer term shows that in addition to morphotypic characteristics physiotypic characteristics are important for space occupation and niche acquisition of the plants in the restinga.     

Ecophysiology of Crassulacean Acid Metabolism (CAM)

BACKGROUND AND SCOPE: Crassulacean Acid Metabolism (CAM) as an ecophysiological modification of photosynthetic carbon acquisition has been reviewed extensively before. Cell biology, enzymology and the flow of carbon along various pathways and through various cellular compartments have been well documented and discussed. The present attempt at reviewing CAM once again tries to use a different approach, considering a wide range of inputs, receivers and outputs. INPUT: Input is given by a network of environmental parameters. Six major ones, CO(2), H(2)O, light, temperature, nutrients and salinity, are considered in detail, which allows discussion of the effects of these factors, and combinations thereof, at the individual plant level ('physiological aut-ecology'). RECEIVERS: Receivers of the environmental cues are the plant types genotypes and phenotypes, the latter including morphotypes and physiotypes. CAM genotypes largely remain 'black boxes', and research endeavours of genomics, producing mutants and following molecular phylogeny, are just beginning. There is no special development of CAM morphotypes except for a strong tendency for leaf or stem succulence with large cells with big vacuoles and often, but not always, special water storage tissues. Various CAM physiotypes with differing degrees of CAM expression are well characterized. OUTPUT: Output is the shaping of habitats, ecosystems and communities by CAM. A number of systems are briefly surveyed, namely aquatic systems, deserts, salinas, savannas, restingas, various types of forests, inselbergs and paramós. CONCLUSIONS: While quantitative census data for CAM diversity and biomass are largely missing, intuition suggests that the larger CAM domains are those systems which are governed by a network of interacting stress factors requiring versatile responses and not systems where a single stress factor strongly prevails. CAM is noted to be a strategy for variable, flexible and plastic niche occupation rather than lush productivity. 'Physiological syn-ecology' reveals that phenotypic plasticity constitutes the ecophysiological advantage of CAM.     

Cladogram of Panamanian Clusia Based on Nuclear DNA: Implications for the Origins of Crassulacean Acid Metabolism

Abstract: The internal transcribed spacer (ITS) region of 18-26S nuclear ribosomal DNA repeat was sequenced for 31 of the approximately 40 species of Clusia known to occur in Panama. Several species from other genera of the Clusiaceae were used as outgroups in the phylogenetic calculation. High sequence alignment and minimal length variation among ITS-1, 5.8S and ITS-2 sequences facilitated determination of positional homology of nucleotide sizes. Sequence alignment was evaluated with character state (Maximum Parsimony) and distance methods (Neighbour Joining). Phylogenetic trees obtained with the two methods were largely concordant and revealed three main groups that roughly correspond to previous arrangements of species into three large morphological groups, the C. flava group, the C. minor group and the C. multiflora group. Because species of Clusia are either regular C₃ plants or exhibit crassulacean acid metabolism (CAM) involving varying proportions of CO₂ fixation in the dark versus the light, we mapped photosynthetic pathways onto the cladograms. Photosynthetic pathway classification was based on measurements of ¹³C/¹²C ratios of plant carbon and also on information available from the literature. Both the C. flava and C. minor group contained species exhibiting CAM, distributed on distinct branches of the cladograms, whereas the third group ( C. multiflora group) was composed of species which are not known to use CAM.     

Expression of crassulacean acid metabolism in <Emphasis Type="Italic">Clusia hilariana</Emphasis> Schlechtendal in different stages of development in the field

Expression of crassulacean acid metabolism (CAM) in the obligate CAM-tree Clusia hilariana SCHLTDL. was studied in the restinga of Jurubatiba National Park, on the Atlantic coast of Rio de Janeiro state, Brazil, comparing plants at different developmental stages. Between young and mature plants there were trends of differences in six parameters, which are all related to CAM expression. From young to mature plants there were tendencies for a decrease of (1) the degree of succulence, (2) the degree of day/night changes of malic acid levels, (3) titratable acidity with nocturnal acid accumulation, (4) the degree of day/night changes of free hexoses with nocturnal break down, (5) effective quantum use efficiency of photosystem II at high photosynthetic photon flux density, and (6) protection from photoinhibition. These tendencies form a clear pattern which suggests that CAM was somewhat more pronounced in leaves of young plants than in leaves of mature plants. A developmental regulation may be involved. However, the observations are probably best explained by stress, since in the dry soils of the restinga young plants have no access to the ground water table while adult trees develop extensive root systems.     

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.     

On the nature of facultative and constitutive CAM: environmental and developmental control of CAM expression during early growth of Clusia, Kalanchöe, and Opuntia

The capacity to induce crassulacean acid metabolism developmentally (constitutive CAM) and to up-regulate CAM expression in response to drought stress (facultative CAM) was studied in whole shoots of seven species by measuring net CO(2) gas exchange for up to 120 day-night cycles during early growth. In Clusia rosea, CAM was largely induced developmentally. Well-watered seedlings began their life cycle as C(3) plants and developed net dark CO(2) fixation indicative of CAM after the initiation of the fourth leaf pair following the cotyledons. Thereafter, CAM activity increased progressively and drought stress led to only small additional, reversible increases in dark CO(2) fixation. In contrast, CAM expression was overwhelmingly under environmental control in seedlings and mature plants of Clusia pratensis. C(3)-type CO(2) exchange was maintained under well-watered conditions, but upon drought stress, CO(2) exchange shifted, in a fully reversible manner, to a CAM-type pattern. Clusia minor showed CO(2) exchange reponses intermediate to those of C. rosea and C. pratensis. Clusia cretosa operated in the C(3) mode at all times. Notably, reversible stress-induced increases of dark CO(2) fixation were also observed during the developmental progression to pronounced CAM in young Kalancho? daigremontiana and Kalancho? pinnata, two species considered constitutive CAM species. Drought-induced up-regulation of CAM was even detected in young cladodes of a cactus, Opuntia ficus-indica, an archetypal constitutive CAM species. Evidently, the defining characteristics of constitutive and facultative CAM are shared, to variable degrees, by all CAM species.     

Drought-stress-induced up-regulation of CAM in seedlings of a tropical cactus, Opuntia elatior, operating predominantly in the C3 mode

Immediately after unfolding, cotyledons of the tropical platyopuntoid cactus, Opuntia elatior Mill., exhibited a C(3)-type diel CO(2) exchange pattern characterized by net CO(2) uptake in the light. Significant nocturnal increases in titratable acidity typical of crassulacean acid metabolism (CAM) were not detected at this early developmental stage. As cotyledons matured and the first cladode (flattened stem) developed, features of CAM were observed and the magnitude of CAM increased. Nonetheless, in well-watered seedlings up to 10 cm tall, C(3) photosynthetic CO(2) fixation in the light remained the major pathway of carbon fixation. Reduced soil water availability led to an up-regulation of net dark CO(2) fixation and greater nocturnal increases in tissue acidity, consistent with facultative CAM. These observations demonstrate that C(3) photosynthesis, drought-stress-related facultative CAM, and developmentally controlled constitutive CAM can all contribute to the early growth of O. elatior. The strong C(3) component and facultative CAM features expressed in young O. elatior contrast with mature plants in which obligate CAM is the major pathway of carbon acquisition.     

Phytochrome-mediated responses of cells and protoplasts of green calli obtained from the leaves of a CAM plant

Green callus obtained from leaves of the CAM-inducible plant Kalanchoe blossfeldiana cv. Montezuma has previously been shown to perform C₃-type photosynthesis under 16-h days and to shift to crassulacean acid metabolism (CAM) under 9-h days. The utilization of photoperiodic regimes (i.e. night interruptions by 30 min red light) established that CAM induction in the callus was under the control of phytochrome, as shown by measurements of CAM criteria: phosphoenolpyruvate carboxylase activity and malic acid pools. Short-term responsiveness of the callus cells to phytochrome modulations by monochromatic radiations was also established by the rapid changes observed in the diameter of the callus-derived protoplasts. These results provide further evidence that whole plant correlations are not necessary for phytochrome operativity.Abbreviations CAM crassulacean acid metabolism - PAL phenylalanine ammonia lyase (EC 4.3.1.5) - PAR photosynthetically active radiations - PEPC phosphoenolpyruvate carboxylase (EC 4.1.1. 31) - Rubisco ribulose 1,5 bisphosphate carboxylase (EC 4.1.1.39)     

The occurrence of crassulacean acid metabolism in Cymbidium (Orchidaceae) and its ecological and evolutionary implications

Crassulacean acid metabolism (CAM) is one of the photosynthetic pathways regarded as adaptations to water stress in land plants. Little is known about correlations among the level of CAM activity, environment of habitat, life form, and phylogenetic relationship of a plant group from an evolutionary perspective. We examined these relationships in 18 species of Cymbidium (Orchidaceae) because the genus shows distinctive diversification of habitats and life forms. The photosynthetic type was classed into three categories, strong CAM, weak CAM, and C₃ on the basis of CAM activity. CAM expression in Cymbidium was confined to the epiphytic and lithophytic species. Especially, all of these species from tropical to subtropical rainforest exhibited CAM activity. On the other hand, the terrestrial species always exhibited C₃ metabolism irrespective of their varied habitats. Regarding the evolution of photosynthetic characters, weak CAM was the ancestral state in Cymbidium and strong CAM and C₃ metabolism occurred subsequently. The evolution of strong CAM likely enabled Cymbidium to extend to exposed sites in tropical lowland where marked water stress exists. Further, different levels of CAM activity characterized each species and such potential plasticity of CAM may realize the radiation of Cymbidium into sites with different environmental conditions.