Leaf anatomical and carbon isotope ratio (δ13C) data from previous studies suggest that the species of the Melastomataceae perform C3 photosynthesis and that leaf anatomical features of some epiphytic taxa resemble the characteristics found in CAM plants. The δ13C values of 67 species of neotropical Melastomataceae (including epiphytes) were obtained from herbarium material deposited at the California Academy of Sciences for assessing the presence of the CAM pathway. The δ13C values obtained from leaves (−23.4‰ to −34.5‰) were congruent with C3 photosynthesis (< −20‰), and the δ13C data from terrestrial (56 samples) and epiphytic species (11 samples) were not statistically different. Our results suggest that CAM photosynthesis is not found in neotropical Melastomataceae. The leaf anatomical features found in some species of Melastomataceae represent adaptations to cope with water stress and are not necessarily correlated with CAM photosynthesis. Photosynthetic pathways can be assessed with the use of leaf anatomical and δ13C data, but further biochemical assays are warranted to corroborate the absence of the CAM pathway in the Melastomataceae.

In the tropical forest of Barro Colorado Island, habitat characteristics, diel acidity changes, CO2 uptake and growth were investigated for the epiphytic cactus Epiphyllum phyllanthus (L.) Haw. It occurred most frequently in tree cavities with its roots in canopy soil and was especially abundant on two tree species: Platypodium elegans J. Vogel and Tabebuia guayacan (Seem.) Hemsl. Its maximum net CO2 uptake rates were low under natural conditions (1.4 μmol m−1) but were comparable to those of other CAM and C3 epiphytes under wet conditions in a screenhouse. Under both natural conditions and in the screenhouse, partial shade enhanced growth and CAM activity. When plants grew under a photosynthetic photon flux of c. 4 mol m−2 d−1, their nocturnal acidity increase and total net CO2 uptake were twice as much as for plants growing at lower (an average of 2.4 mol m−2 d−1) and higher (7.7 mol m−2 d−1) photosynthetic photon fluxes. Stem elongation was 27% greater at the intermediate photosynthetic photon flux. Seedlings of E. phyllanthus survived three months of drought and responded rapidly to rewetting, recovering fully within three days. Transpiration rates and nocturnal acidity increases also recovered to the values of well-watered plants a few days after rewetting, indicating that this species can take advantage of episodic rainfall during the dry season.

Dew deposition was calculated for leaves of the epiphytic bromeliads Tillandsia brachycaulos and T. elongata in a tropical dry deciduous forest in Yucatán, Mexico, over one year. Plant characteristics and water relations were also measured. Estimations were made by using energy balance analysis and the Penman–Monteith equation. Dew accumulation was also quantified using a cloth-plate method and by change in mass of whole plants. Tissue water content and total leaf area were similar in the two species, but maximum tank water content was three-fold greater for T. elongata than for T. brachycaulos, which had a lower degree of tissue desiccation tolerance than T. elongata. Succulence for T. brachycaulos changed little during most of the year, decreasing significantly only during one month in the dry season. Leaf water potential and osmotic pressure did not change significantly after a dew-deposition event. Theoretical dew per night on leaves was greatest during the early dry season (about 0.72 mm) compared with 0.34 mm in the rainy season and 0.008 mm in the late dry season. Dew amounts alone are not adequate to support growth but may maintain a favourable water balance for epiphytic bromeliads during the driest months of the year.

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.

Responses of gas exchange and photosynthesis to changes in CO2 concentration and PPFD were examined in well watered plants of Delosperma tradescantioides Bgr. to establish the relative importance of these environmental changes on the photosynthetic machinery in this CAM-cycling species which grows naturally in both exposed and partly shaded environments. Plants were grown at two PPFDs (220 [LL] and 550 [HL] μmol m−2 s−1). HL plants had larger leaves with higher specific weight, water content and diurnal malic acid fluctuation. Photosynthetic PPFD responses were typically those of sun and shade species for HL and LL plants, both under 21% O2 and non-photorespiratory (2% O2) conditions. The CO2 compensation point in the absence of non-photorespirational CO2 evolution in the light (Γ∗) was c. 30 μmol mol−1. Irradiation reduced mitochondrial respiration by >50%. Comparison of the PPFD responses of linear electron flow rates derived from gas exchange measurements and from fluorescence analysis ([Jscr ]F) indicated effective photosynthetic control. [Jscr ]F was always larger than electron flow rates calculated from gas exchange, indicating that processes other than carboxylation and oxygenation were consistently important in energy consumption under all sampled environmental conditions. Regardless of PPFD during growth, electron flow to carboxylation and [Jscr ]F were linearly correlated, demonstrating that the photosynthetic apparatus was well adapted to PPFD during growth. In HL plants, non-photochemical quenching increased, and photochemical quenching and the quantum yield of linear electron transport through PS II decreased more slowly with increasing PPFD than in LL plants. In plants of both treatments non-photochemical energy dissipation seemed to be exhausted when the proportion of photons not utilizable by photochemistry exceeded 0·7. Results illustrate a pronounced ability of D. tradescantioides to acclimate to a 100% change in the prevailing PPFD and lend support to the hypothesis that CAM cycling might act as a photoprotective process.

The occurrence of crassulacean acid metabolism (CAM) among the epiphyte flora of the lowland forest on Barro Colorado Island (BCI), Panama, was investigated. A total of 116 species was included, i.e. about 2/3 of the known epiphyte taxa. As judged from the carbon isotope ratios and the absence of Kranz anatomy, indications of CAM were found in 29 species of three families, Orchidaceae (20), Bromeliaceae (7), and Cactaceae (2). We estimate that about 25% of the epiphyte flora of BCI are CAM plants. CAM was most prevalent in exposed sites, but even in the understorey two epiphyte species engage in CAM.