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Crassulacean Acid Metabolism in Epiphytic Orchids: Current Knowledge, Future Perspectives
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1982.tb13297.xopenalex-snapshot
ROOTS OF SOBRALIA MACRANTHA (ORCHIDACEAE): STRUCTURE AND FUNCTION OF THE VELAMEN‐EXODERMIS COMPLEX
inferredcites →https://doi.org/10.1002/j.1537-2197.1983.tb12440.xopenalex-snapshot
SHOOTLESSNESS, VELAMENTOUS ROOTS, AND THE PRE‐EMINENCE OF ORCHIDACEAE IN THE EPIPHYTIC BIOTOPE
inferredcites →https://doi.org/10.1002/j.1537-2197.1990.tb13585.xopenalex-snapshot
ROLE OF PSEUDOBULBS IN GROWTH AND FLOWERING OF CATASETUM VIRIDIFLAVUM (ORCHIDACEAE)
inferredcites →https://doi.org/10.1006/anbo.1999.0983openalex-snapshot
What are Backshoots Good For? Seasonal Changes in Mineral, Carbohydrate and Water Content of Different Organs of the Epiphytic Orchid, Dimerandra emarginata
inferredcites →https://doi.org/10.1007/978-3-642-13145-5_14openalex-snapshot
Photorespiration in Phase III of Crassulacean Acid Metabolism: Evolutionary and Ecophysiological Implications
inferredcites →https://doi.org/10.1007/978-3-642-74465-5_2openalex-snapshot
The Evolution of Epiphytism
inferredcites →https://doi.org/10.1007/978-3-642-79060-7_1openalex-snapshot
An Introduction to Crassulacean Acid Metabolism. Biochemical Principles and Ecological Diversity
inferredcites →https://doi.org/10.1007/978-94-010-9013-1_12openalex-snapshot
Crassulacean acid metabolism
inferredcites →https://doi.org/10.1007/bf00345168openalex-snapshot
Seasonal shift from C3 photosynthesis to Crassulacean Acid Metabolism in Mesembryanthemum crystallinum growing in its natural environment
inferredcites →https://doi.org/10.1007/bf00376985openalex-snapshot
Carbon dioxide assimilation in the flowerhead of Arctium
inferredcites →https://doi.org/10.1007/bf00377173openalex-snapshot
Photosynthesis by flowers in Encelia farinosa and Encelia californica (Asteraceae)
inferredcites →https://doi.org/10.1007/bf00379345openalex-snapshot
The carbon balance of flowers of Diplacus aurantiacus (Scrophulariaceae)
inferredcites →https://doi.org/10.1007/bf00379417openalex-snapshot
Altitudinal changes in the incidence of crassulacean acid metabolism in vascular epiphytes and related life forms in Papua New Guinea
inferredcites →https://doi.org/10.1007/bf00379570openalex-snapshot
Crassulacean acid metabolism in australian vascular epiphytes and some related species
inferredcites →https://doi.org/10.1007/s00442-003-1418-xopenalex-snapshot
How prevalent is crassulacean acid metabolism among vascular epiphytes?
inferredcites →https://doi.org/10.1007/s00468-005-0413-8openalex-snapshot
Carbon isotope composition of canopy leaves in a tropical forest in Panama throughout a seasonal cycle
inferredcites →https://doi.org/10.1007/s10265-007-0144-6openalex-snapshot
The occurrence of crassulacean acid metabolism in Cymbidium (Orchidaceae) and its ecological and evolutionary implications
inferredcites →https://doi.org/10.1007/s11099-008-0090-0openalex-snapshot
Carbon isotope ratios and the variation in the diurnal pattern of malate accumulation in aerial roots of CAM species of Phalaenopsis (Orchidaceae)
inferredcites →https://doi.org/10.1007/s11099-010-0007-6openalex-snapshot
The photosynthetic pathway of the roots of twelve epiphytic orchids with CAM leaves
inferredcites →https://doi.org/10.1007/s11258-010-9765-2openalex-snapshot
Comparative water balance profiles of Orchidaceae seeds for epiphytic and terrestrial taxa endemic to North America
inferredcites →https://doi.org/10.1016/0304-4238(92)90106-mopenalex-snapshot
Calvin cycle activity in fruit and the effect of heat stress
inferredcites →https://doi.org/10.1016/b978-0-12-294302-7.50016-1openalex-snapshot
Crassulacean Acid Metabolism (CAM)
inferredcites →https://doi.org/10.1016/j.flora.2008.08.003openalex-snapshot
Anatomy and photosynthetic parameters of roots and leaves of two shade-adapted orchids, Dichaea cogniauxiana Shltr. and Epidendrum secundum Jacq.
inferredcites →https://doi.org/10.1016/j.jplph.2009.10.011openalex-snapshot
Specific leaf areas of the tank bromeliad Guzmania monostachia perform distinct functions in response to water shortage
inferredcites →https://doi.org/10.1016/s0031-9422(00)82244-xopenalex-snapshot
Crassulacean Acid Metabolism: Analysis of an Ecological Adaptation
inferredcites →https://doi.org/10.1016/s0044-328x(72)80131-4openalex-snapshot
NaCl-induzierter crassulaceensäurestoffwechsel bei Mesembryanthemum crystallinum
inferredcites →https://doi.org/10.1016/s0098-8472(98)00024-0openalex-snapshot
Pattern of photoassimilate partitioning in pseudobulbous and rhizomatous terrestrial orchids
inferredcites →https://doi.org/10.1016/s0098-8472(98)00042-2openalex-snapshot
Susceptibility of CAM Dendrobium leaves and flowers to high light and high temperature under natural tropical conditions
inferredcites →https://doi.org/10.1016/s0176-1617(85)80166-8openalex-snapshot
Crassulacean Acid Metabolism in Roots of a Leafless Orchid, Campylocentrum tyrridion Garay & Dunsterv.
inferredcites →https://doi.org/10.1016/s0176-1617(88)80141-xopenalex-snapshot
Interaction of Photoperiod and Drought as CAM Inducing Factors in Kalanchoë blossfeldiana Poelln., cv. Tom Thumb.
inferredcites →https://doi.org/10.1016/s0304-4238(99)00084-9openalex-snapshot
Orchid pseudobulbs – `false' bulbs with a genuine importance in orchid growth and survival!
inferredcites →https://doi.org/10.1016/s0981-9428(01)01321-3openalex-snapshot
Effect of a drought period on the mobilisation of non-structural carbohydrates, photosynthetic efficiency and water status in an epiphytic orchid
inferredcites →https://doi.org/10.1023/a:1006006331011openalex-snapshot
Identification of phosphoenolpyruvate carboxylase isoforms in leaf, stem and roots of the obligate CAM plant Vanilla planifolia Salib. (Orchidaceae): a physiological and molecular approach
inferredcites →https://doi.org/10.1023/a:1006807900507openalex-snapshot
Photosynthetic utilization of radiant energy by CAM Dendrobium flowers
inferredcites →https://doi.org/10.1034/j.1399-3054.1995.930310.xopenalex-snapshot
The contribution of fruit photosynthesis to the carbon requirement of cucumber fruits as affected by irradiance, temperature and ontogeny
inferredcites →https://doi.org/10.1038/35021000openalex-snapshot
Atmospheric carbon dioxide concentrations over the past 60 million years
inferredcites →https://doi.org/10.1038/nature06039openalex-snapshot
Dating the origin of the Orchidaceae from a fossil orchid with its pollinator
inferredcites →https://doi.org/10.1046/j.0016-8025.2001.00760.xopenalex-snapshot
Induction of Crassulacean acid metabolism by water limitation
inferredcites →https://doi.org/10.1046/j.1365-3040.2000.00588.xopenalex-snapshot
Responses of CAM species to increasing atmospheric CO2 concentrations
inferredcites →https://doi.org/10.1046/j.1469-8137.1997.00800.xopenalex-snapshot
The occurrence of crassulacean acid metabolism among vascular epiphytes from Central Panama
inferredcites →https://doi.org/10.1046/j.1469-8137.2002.00489.xopenalex-snapshot
Carbon isotope ratio and the extent of daily CAM use by Bromeliaceae
inferredcites →https://doi.org/10.1071/fp04179openalex-snapshot
Distribution of crassulacean acid metabolism in orchids of Panama: evidence of selection for weak and strong modes
inferredcites →https://doi.org/10.1071/fp05079openalex-snapshot
Large gene family of phosphoenolpyruvate carboxylase in the crassulacean acid metabolism plant Kalanchoe pinnata (Crassulaceae) characterised by partial cDNA sequence analysis
inferredcites →https://doi.org/10.1071/fp10084openalex-snapshot
Evolution along the crassulacean acid metabolism continuum
inferredcites →https://doi.org/10.1071/pp01193openalex-snapshot
Resistance is useful: diurnal patterns of photosynthesis in C 3 and crassulacean acid metabolism epiphytic bromeliads
inferredcites →https://doi.org/10.1071/pp9790557openalex-snapshot
Crassulacean Acid Metabolism and Diurnal Variations of Internal CO2 and O2 Concentrations in Sedum praealtum DC
inferredcites →https://doi.org/10.1078/0367-2530-00080openalex-snapshot
Non-foliar photosynthesis – a strategy of additional carbon acquisition
inferredcites →https://doi.org/10.1086/284681openalex-snapshot
Reproductive Effort in Plants. 1. Carbon Allocation to Reproduction
inferredcites →https://doi.org/10.1086/297240openalex-snapshot
Partitioning of14C Assimilates between Sources and Sinks During Different Growth Stages in the Sympodial Thin-Leaved Orchid Oncidium Goldiana
inferredcites →https://doi.org/10.1086/335966openalex-snapshot
The Role of the Velamen of the Aerial Roots of Orchids
inferredcites →https://doi.org/10.1086/337303openalex-snapshot
Crassulacean Acid Metabolism in Orchids under Water Stress
inferredcites →https://doi.org/10.1086/407590openalex-snapshot
Mineral Nutrition and Related Phenomena in Bromeliaceae and Orchidaceae
inferredcites →https://doi.org/10.1093/aob/mch087openalex-snapshot
Ecophysiology of Crassulacean Acid Metabolism (CAM)
inferredcites →https://doi.org/10.1093/aob/mcn145openalex-snapshot
Crassulacean acid metabolism and fitness under water deficit stress: if not for carbon gain, what is facultative CAM good for?
inferredcites →https://doi.org/10.1093/jexbot/52.364.2067openalex-snapshot
The physiological ecology of vascular epiphytes: current knowledge, open questions
inferredcites →https://doi.org/10.1093/jxb/42.4.493openalex-snapshot
Occurrence of Inducible Crassulacean Acid Metabolism in Leaves ofTalimum triangulare(Portulacaceae)
inferredcites →https://doi.org/10.1093/jxb/ern080openalex-snapshot
On the nature of facultative and constitutive CAM: environmental and developmental control of CAM expression during early growth of Clusia, Kalanchoe, and Opuntia
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a085907openalex-snapshot
Occurrence of Non-functional Stomata in the Flowers of Tropical Orchids
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a075683openalex-snapshot
Effect of leaf age on light and dark 14CO2 fixation in a CAM plant, Bryophyllum calycinum
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a076498openalex-snapshot
Change in Properties of Phosphoenolpyruvate Carboxylase in Kalanchoe daigremontiana with Leaf Age
inferredcites →https://doi.org/10.1104/pp.010818openalex-snapshot
Crassulacean Acid Metabolism. A Plastic Photosynthetic Adaptation to Arid Environments
inferredcites →https://doi.org/10.1104/pp.108.132555openalex-snapshot
Crassulacean Acid Metabolism and Epiphytism Linked to Adaptive Radiations in the Orchidaceae
inferredcites →https://doi.org/10.1104/pp.43.1.130openalex-snapshot
Photosynthetic 14CO2 Fixation by Green Cymbidium (Orchidaceae) Flowers
inferredcites →https://doi.org/10.1104/pp.53.4.581openalex-snapshot
Variation in the Carbon Isotope Composition of a Plant with Crassulacean Acid Metabolism
inferredcites →https://doi.org/10.1104/pp.77.1.83openalex-snapshot
Photosynthetic Carbon Assimilation in a Shootless Orchid, Chiloschista usneoides (DON) LDL
inferredcites →https://doi.org/10.1104/pp.87.2.454openalex-snapshot
Stimulation of CAM Photosynthesis in Kalanchoë blossfeldiana by Transferring to Nitrogen-Deficient Conditions
inferredcites →https://doi.org/10.1104/pp.87.3.666openalex-snapshot
Photosynthetic Activities in the Petunia Corolla
inferredcites →https://doi.org/10.1111/j.1095-8339.2010.01058.xopenalex-snapshot
The incidence of crassulacean acid metabolism in Orchidaceae derived from carbon isotope ratios: a checklist of the flora of Panama and Costa Rica
inferredcites →https://doi.org/10.1111/j.1469-8137.1969.tb06469.xopenalex-snapshot
PARTIAL IDENTIFICATION OF DARK 14CO2 FIXATION PRODUCTS IN LEAVES OF CATTLEYA (ORCHIDACEAE)
inferredcites →https://doi.org/10.1111/j.1469-8137.1977.tb04840.xopenalex-snapshot
DIURNAL STOMATAL AND ACIDITY RHYTHMS IN ORCHID LEAVES
inferredcites →https://doi.org/10.1111/j.1469-8137.1979.tb07577.xopenalex-snapshot
PHOTOSYNTHETIC CONTRIBUTION OF FLOWERS AND SEEDS TO REPRODUCTIVE EFFORT OF AN ANNUAL COLONIZER
inferredcites →https://doi.org/10.1111/j.1469-8137.1983.tb02688.xopenalex-snapshot
RHYTHMS OF ACIDITY AND CO2 PRODUCTION IN ORCHID FLOWERS
inferredcites →https://doi.org/10.1111/j.1469-8137.1983.tb03504.xopenalex-snapshot
CARBON FIXATION IN ORCHID AERIAL ROOTS
inferredcites →https://doi.org/10.1111/j.1469-8137.1984.tb03585.xopenalex-snapshot
CRASSULACEAN ACID METABOLISM IN YOUNG ORCHID LEAVES
inferredcites →https://doi.org/10.1111/j.1469-8137.1990.tb00406.xopenalex-snapshot
The stimulation of CAM activity in Mesembryanthemum crystallinum in nitrate and phosphate‐deficient conditions
inferredcites →https://doi.org/10.1142/5505openalex-snapshot
The Physiology of Tropical Orchids in Relation to the Industry
inferredcites →https://doi.org/10.1146/annurev.pp.11.060160.000501openalex-snapshot
Crassulacean Acid Metabolism
inferredcites →https://doi.org/10.1146/annurev.pp.24.060173.001345openalex-snapshot
Photosynthetic Carbon Fixation in Relation to Net CO2 Uptake
inferredcites →https://doi.org/10.1146/annurev.pp.29.060178.002115openalex-snapshot
Crassulacean Acid Metabolism: A Curiosity in Context
inferredcites →https://doi.org/10.15517/lank.v3i2.23028openalex-snapshot
Why are there so many orchid species?
inferredcites →https://doi.org/10.1590/s0102-33062001000200004openalex-snapshot
Morfo-anatomia caulinear de nove espécies de Orchidaceae
inferredcites →https://doi.org/10.1626/pps.13.256openalex-snapshot
Crassulacean Acid Metabolism May Alleviate Production of Reactive Oxygen Species in a Facultative CAM Plant, the Common Ice PlantMesembryanthemum crystallinumL.
inferredcites →https://doi.org/10.2307/1295415openalex-snapshot
Properties of Some Natural Waters in a Tropical Wet Forest of Costa Rica
inferredcites →https://doi.org/10.2307/2387715openalex-snapshot
Vegetative Reduction in Epiphytic Bromeliaceae and Orchidaceae: Its Origin and Significance
inferredcites →https://doi.org/10.2307/2389294openalex-snapshot
Carbon Isotope Ratios of Plants of a Tropical Dry Forest in Mexico
inferredcites →https://doi.org/10.2307/2399394openalex-snapshot
Vascular Epiphytism: Taxonomic Participation and Adaptive Diversity
inferredcites →https://doi.org/10.2307/2399395openalex-snapshot
Diversity and Biogeography of Neotropical Vascular Epiphytes
inferredcites →https://doi.org/10.2307/2445813openalex-snapshot
Reproductive effort and floral photosynthesis in Spiranthes cernua (Orchidaceae)
inferredcites →https://doi.org/10.2307/3668590openalex-snapshot
Pseudobulb Structure in Some Boreal Terrestrial Orchids
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.15446/caldasia.v46n2.106005zenodo-depositor-declared
Descripción taxonómica y funcional de un ensamblaje de epífitas vasculares en la Cordillera Occidental Colombiana
inferred← citeshttps://doi.org/10.1002/jsfa.8501openalex-snapshot
Targeting carbon for crop yield and drought resilience
inferred← citeshttps://doi.org/10.1007/978-3-319-93594-2_10openalex-snapshot
Functional Anatomical Traits of the Photosynthetic Organs of Plants with Crassulacean Acid Metabolism
inferred← citeshttps://doi.org/10.1007/s00018-014-1767-0openalex-snapshot
General mechanisms of drought response and their application in drought resistance improvement in plants
inferred← citeshttps://doi.org/10.1007/s11120-017-0466-8openalex-snapshot
Anatomical and diffusional determinants inside leaves explain the difference in photosynthetic capacity between Cypripedium and Paphiopedilum, Orchidaceae
inferred← citeshttps://doi.org/10.1007/s11120-021-00826-2openalex-snapshot
Photosynthetic electron transport rate (ETR) in the littoral herb Launaea sarmentosa known as mole crab in Thailand
inferred← citeshttps://doi.org/10.1016/j.jplph.2020.153187openalex-snapshot
Photosynthesis in a Vanda sp orchid with Photosynthetic Roots
inferred← citeshttps://doi.org/10.1016/j.pld.2018.06.003openalex-snapshot
Physiological diversity of orchids
inferred← citeshttps://doi.org/10.1093/aob/mct090openalex-snapshot
Spatial patterns of photosynthesis in thin- and thick-leaved epiphytic orchids: unravelling C3–CAM plasticity in an organ-compartmented way
inferred← citeshttps://doi.org/10.1111/ecog.05410openalex-snapshot
Functional traits are key to understanding orchid diversity on islands
inferred← citeshttps://doi.org/10.1134/s1021443726604556openalex-snapshot
CAM Plants under Global Climate Change: Genetic, Metabolic, and Ecophysiological Aspects
inferred← citeshttps://doi.org/10.1134/s2079086422050073openalex-snapshot
CAM (Crassulacean Acid Metabolism) Photosynthesis in Vascular Epiphytes
inferred← citeshttps://doi.org/10.11606/d.41.2016.tde-14012016-165804openalex-snapshot
Caracterização da capacidade de indução ao CAM em plantas de Vriesea gigantea (Bromeliaceae) sob déficit hídrico.
inferred← citeshttps://doi.org/10.11606/t.41.2017.tde-02122016-095125openalex-snapshot
Sinalização do óxido nítrico sobre a regulação do Metabolismo Ácido das Crassuláceas (CAM) em Guzmania monostachia
inferred← citeshttps://doi.org/10.1186/s40529-019-0255-0openalex-snapshot
CAM plasticity in epiphytic tropical orchid species responding to environmental stress
inferred← citeshttps://doi.org/10.1560/ijps.60.3.385openalex-snapshot
Carbon exchange rate of pitahaya (Hylocereus undatus L. Harwort) in contrasting seasons and irrigation regimes
inferred← citeshttps://doi.org/10.21829/abm128.2021.1827openalex-snapshot
Diversidad de epífitas vasculares en árboles remanentes del género Ficus (Moraceae) en sistemas silvopastoriles del sureste de México
inferred← citeshttps://doi.org/10.23910/1.2022.3115aopenalex-snapshot
Adaptational Mechanisms of Epiphytic Orchids: A Review
inferred← citeshttps://doi.org/10.26656/fr.2017.7(3).008openalex-snapshot
Qualitative phytochemical analysis, enzymatic and non-enzymatic antioxidant activities in stems and leaves of Vanilla planifolia (Orchidaceae)
inferred← citeshttps://doi.org/10.3389/ffgc.2022.828851openalex-snapshot
Diversity and Vertical Distribution of Epiphytic Angiosperms, in Natural and Disturbed Forest on the Northern Coast of Jalisco, Mexico
inferred← citeshttps://doi.org/10.5772/56219openalex-snapshot
CAM Photosynthesis in Bromeliads and Agaves: What Can We Learn from These Plants?
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