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Desiccation tolerant vascular plants of southern Africa
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Index, der aus Deutsch‐Südwestafrika bis zum Jahre 1917 bekannt gewordenen Pflanzenarten. V.
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Zur Kenntnis einer xerophilen Wasserpflanze: Chamaegigas intrepidus DTR. aus Südwestafrika
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A PHYSIOLOGICAL AND ANATOMICAL STUDY OF THE LEAVES OF POLYPODIUM POLYPODIOIDES
inferredcites →https://doi.org/10.1002/jpln.19550690139openalex-snapshot
Paech, K., und Tracey, M. V.: Moderne Methoden der Pflanzenanalyse. Band II. XII + 626 Seiten. Springer-Verlag, Berlin-Göttingen-Heidelberg 1955. Geb. 110.— DM
inferredcites →https://doi.org/10.1007/bf00385023openalex-snapshot
Revival of respiration and photosynthesis in dried leaves of Polypodium polypodioides
inferredcites →https://doi.org/10.1007/bf01911097openalex-snapshot
Über die gravimetrische Methode zur Bestimmung der Saugspannung und das Problem des negativen Turgors
inferredcites →https://doi.org/10.1007/bf01917151openalex-snapshot
Untersuchungen über die Saugkraft der Pflanzen
inferredcites →https://doi.org/10.1016/s0006-3495(66)86685-7openalex-snapshot
Physical Properties of Cell Water in Partially Dried Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1038/1911415a0openalex-snapshot
A Poikilohydrous, Poikilochlorophyllous Angiosperm from Africa
inferredcites →https://doi.org/10.1071/bi9580349openalex-snapshot
The Measurement of Diffusion Pressure Deficit in Plants by a Method of Vapour Equilibration
inferredcites →https://doi.org/10.1071/bt9760209openalex-snapshot
Borya nitida Labill.—An Australian Species in the Liliaceae With Desiccation-tolerant Leaves
inferredcites →https://doi.org/10.1071/bt9760225openalex-snapshot
The Fine Structure of Dehydrated and Reviving Leaves of Borya nitida Labill.—A Desiccation-tolerant Plant
inferredcites →https://doi.org/10.1093/jaoac/39.3.895bopenalex-snapshot
Modern Methods of Plant Analysis
inferredcites →https://doi.org/10.1093/jxb/22.3.756openalex-snapshot
The Use of Non-permeating Pigments for Testing the Survival of Cells
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a089778openalex-snapshot
On the Behaviour during Drought of Leaves of two Cape Species of Passerina, with some Notes on their Anatomy
inferredcites →https://doi.org/10.1111/j.1399-3054.1959.tb07932.xopenalex-snapshot
Drought Tolerance and Avoidance in Two Species of Oak
inferredcites →https://doi.org/10.1111/j.1438-8677.1969.tb02221.xopenalex-snapshot
Zur Physiologie von Myrothamnus flabellifolia1
inferredcites →https://doi.org/10.1111/j.1469-8137.1914.tb05743.xopenalex-snapshot
“THE FLORA OF SOUTH AFRICA,”
inferredcites →https://doi.org/10.1126/science.174.4013.1033openalex-snapshot
Desiccation-Tolerant Flowering Plants in Southern Africa
inferredcites →https://doi.org/10.2307/2989806openalex-snapshot
Biological and Morphological Aspects of the Velloziaceae
inferredcites →https://doi.org/10.4102/abc.v11i3.1476openalex-snapshot
Southern African grasses with foliage that revives after dehydration
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.449.1.5zenodo-depositor-declared
Rediscovery and new combination of Serpocaulon demissum (Polypodiaceae), an endangered endemic species to the Brazilian inselbergs
inferred← citeshttps://doi.org/10.1002/9780470376881.ch2openalex-snapshot
Lessons on Dehydration Tolerance from Desiccation‐Tolerant Plants
inferred← citeshttps://doi.org/10.1002/9780470376881.ch3openalex-snapshot
Mechanisms of Desiccation Tolerance in Angiosperm Resurrection Plants
inferred← citeshttps://doi.org/10.1002/9780470650608.ch3openalex-snapshot
Desiccation‐Tolerance of Plant Tissues: A Mechanistic Overview
inferred← citeshttps://doi.org/10.1002/9783527632930.ch17openalex-snapshot
A Systems‐Based Molecular Biology Analysis of Resurrection Plants for Crop and Forage Improvement in Arid Environments
inferred← citeshttps://doi.org/10.1002/ajb2.1588openalex-snapshot
Unexplored dimensions of variability in vegetative desiccation tolerance
inferred← citeshttps://doi.org/10.1002/pld3.96openalex-snapshot
A chromosome‐scale assembly of the model desiccation tolerant grass Oropetium thomaeum
inferred← citeshttps://doi.org/10.1006/anbo.1996.0180openalex-snapshot
Differences in Rehydration of Three Desiccation-tolerant Angiosperm Species
inferred← citeshttps://doi.org/10.1006/anbo.1999.0927openalex-snapshot
The Effect of Drying Rate on the Survival of Three Desiccation-tolerant Angiosperm Species
inferred← citeshttps://doi.org/10.1006/anbo.1999.1006openalex-snapshot
Resurrection Plants and the Secrets of Eternal Leaf
inferred← citeshttps://doi.org/10.1007/978-1-4615-3304-7_66openalex-snapshot
Molecular Analysis of Desiccation Tolerance in the Resurrection Plant Craterostigma Plantagineum
inferred← citeshttps://doi.org/10.1007/978-3-319-75103-0_19openalex-snapshot
Desiccation Tolerance in Ferns: From the Unicellular Spore to the Multi-tissular Sporophyte
inferred← citeshttps://doi.org/10.1007/978-3-642-19106-0_12openalex-snapshot
Chamaegigas intrepidus DINTER: An Aquatic Poikilohydric Angiosperm that Is Perfectly Adapted to Its Complex and Extreme Environmental Conditions
inferred← citeshttps://doi.org/10.1007/978-3-642-19106-0_16openalex-snapshot
Resurrection Plants: Physiology and Molecular Biology
inferred← citeshttps://doi.org/10.1007/978-3-642-19106-0_6openalex-snapshot
Ecophysiology of Desiccation/Rehydration Cycles in Mosses and Lichens
inferred← citeshttps://doi.org/10.1007/978-3-642-19106-0_8openalex-snapshot
Evolution, Diversity, and Habitats of Poikilohydrous Vascular Plants
inferred← citeshttps://doi.org/10.1007/978-3-642-19106-0_9openalex-snapshot
Ecophysiology of Homoiochlorophyllous and Poikilochlorophyllous Desiccation-Tolerant Plants and Vegetations
inferred← citeshttps://doi.org/10.1007/978-3-642-59773-2_24openalex-snapshot
Biodiversity of Terrestrial Habitat Islands — the Inselberg Evidence
inferred← citeshttps://doi.org/10.1007/978-3-642-59773-2_8openalex-snapshot
Vascular Plants on Inselbergs: Vegetative and Reproductive Strategies
inferred← citeshttps://doi.org/10.1007/978-3-642-59773-2_9openalex-snapshot
Ecophysiology of Vascular Plants on Inselbergs
inferred← citeshttps://doi.org/10.1007/978-3-642-67873-8_23openalex-snapshot
Experimental Ecology (Ecological Geobotany)
inferred← citeshttps://doi.org/10.1007/978-3-642-68150-9_3openalex-snapshot
Water in Tissues and Cells
inferred← citeshttps://doi.org/10.1007/978-3-642-68150-9_5openalex-snapshot
Water Uptake by Organs Other Than Roots
inferred← citeshttps://doi.org/10.1007/978-3-642-68297-1_18openalex-snapshot
Experimental Ecology (Ecological Geobotany)
inferred← citeshttps://doi.org/10.1007/978-3-642-76682-4_10openalex-snapshot
Desiccation Tolerance in Vegetative Plant Tissues and Seeds: Protein Synthesis in Relation to Desiccation and a Potential Role for Protection and Repair Mechanisms
inferred← citeshttps://doi.org/10.1007/978-3-642-80446-5_11openalex-snapshot
Physiology of Poikilohydric Plants
inferred← citeshttps://doi.org/10.1007/978-981-10-6744-0_2openalex-snapshot
Adaptive Mechanisms of Desiccation Tolerance in Resurrection Plants
inferred← citeshttps://doi.org/10.1007/978-981-10-6744-0_3openalex-snapshot
Dehydration and Freezing Resistance of Lichenized Fungi
inferred← citeshttps://doi.org/10.1007/bf00198578openalex-snapshot
Reconstitution of chlorophylls and photosynthetic CO2 assimilation upon rehydration of the desiccated poikilochlorophyllous plant Xerophyta scabrida (Pax) Th. Dur. et Schinz
inferred← citeshttps://doi.org/10.1007/bf00201352openalex-snapshot
Desiccation leads to the rapid accumulation of both cytosolic and chloroplastic proteins in the resurrection plant Craterostigma plantagineum Hochst
inferred← citeshttps://doi.org/10.1007/bf00201503openalex-snapshot
Abscisic-acid-induced drought tolerance in Funaria hygrometrica Hedw.
inferred← citeshttps://doi.org/10.1007/bf00202321openalex-snapshot
Molecular cloning of abscisic acid-modulated genes which are induced during desiccation of the resurrection plant Craterostigma plantagineum
inferred← citeshttps://doi.org/10.1007/bf00351023openalex-snapshot
Flavonoid tannins — structural wood components for drought-resistance mechanisms of plants
inferred← citeshttps://doi.org/10.1007/bf00377119openalex-snapshot
Desiccation tolerant ?resurrection? grasses from Kenya and West Africa
inferred← citeshttps://doi.org/10.1007/bf00377357openalex-snapshot
Desiccation tolerant plants in South America
inferred← citeshttps://doi.org/10.1007/bf00379117openalex-snapshot
ATP and ADP contents in leaves of drying and rehydrating desiccation tolerant plants
inferred← citeshttps://doi.org/10.1007/bf00540912openalex-snapshot
Drought tolerance of germinating seeds and young seedlings of Anastatica hierochuntica L.
inferred← citeshttps://doi.org/10.1007/bf00649500openalex-snapshot
Early-spring gas exchange and uptake of deuterium-labelled water in the poikilohydric fernPolypodium virginianum
inferred← citeshttps://doi.org/10.1007/bf02909453openalex-snapshot
The effect of dehydration and rehydration on the nitrogen content of various fractions from resurrection plants
inferred← citeshttps://doi.org/10.1007/bf02912748openalex-snapshot
Water use efficiency, photosynthesis, extreme temperature and drought tolerance of desert plant seedlings
inferred← citeshttps://doi.org/10.1007/s00300-017-2249-2openalex-snapshot
Bound water behavior in Cetraria aculeata thalli during freezing
inferred← citeshttps://doi.org/10.1007/s00425-012-1628-8openalex-snapshot
Light response, oxidative stress management and nucleic acid stability in closely related Linderniaceae species differing in desiccation tolerance
inferred← citeshttps://doi.org/10.1007/s00425-015-2320-6openalex-snapshot
A molecular physiological review of vegetative desiccation tolerance in the resurrection plant Xerophyta viscosa (Baker)
inferred← citeshttps://doi.org/10.1007/s00425-016-2631-2openalex-snapshot
The role of peltate scales in desiccation tolerance of Pleopeltis polypodioides
inferred← citeshttps://doi.org/10.1007/s00425-019-03105-6openalex-snapshot
Adaptive responses of amino acid metabolism to the combination of desiccation and low nitrogen availability in Sporobolus stapfianus
inferred← citeshttps://doi.org/10.1007/s00425-025-04752-8openalex-snapshot
Unravelling the molecular network of desiccation tolerance in resurrection plants started with the model plant Craterostigma plantagineum
inferred← citeshttps://doi.org/10.1007/s00792-021-01227-yopenalex-snapshot
A comparative analysis of gaseous phase hydration properties of two lichenized fungi: Niebla tigrina (Follman) Rundel & Bowler from Atacama Desert and Umbilicaria antarctica Frey & I. M. Lamb from Robert Island, Southern Shetlands Archipelago, maritime Antarctica
inferred← citeshttps://doi.org/10.1007/s10531-007-9156-8openalex-snapshot
Plant communities on ironstone outcrops: a diverse and endangered Brazilian ecosystem
inferred← citeshttps://doi.org/10.1007/s10535-009-0070-7openalex-snapshot
Ultrastructural responses of the desiccation tolerant plants Xerophyta viscosa and X. retinervis to dehydration and rehydration
inferred← citeshttps://doi.org/10.1007/s10725-010-9491-8openalex-snapshot
Desiccation tolerance in Pleurostima purpurea (Velloziaceae)
inferred← citeshttps://doi.org/10.1007/s10725-010-9498-1openalex-snapshot
The use of aeroponics to investigate antioxidant activity in the roots of Xerophyta viscosa
inferred← citeshttps://doi.org/10.1007/s10725-010-9514-5openalex-snapshot
Editorial: special issue GROW “plant desiccation stress”
inferred← citeshttps://doi.org/10.1007/s10886-005-8396-xopenalex-snapshot
The South African and Namibian Populations of the Resurrection Plant Myrothamnus flabellifolius are Genetically Distinct and Display Variation in Their Galloylquinic Acid Composition
inferred← citeshttps://doi.org/10.1007/s11258-007-9308-7openalex-snapshot
Biodiversity and spatial distribution of vascular epiphytes in two biotopes of the Cameroonian semi-deciduous rain forest
inferred← citeshttps://doi.org/10.1007/s11427-007-0002-8openalex-snapshot
Protective mechanism of desiccation tolerance in Reaumuria soongorica: Leaf abscission and sucrose accumulation in the stem
inferred← citeshttps://doi.org/10.1007/s11738-011-0891-9openalex-snapshot
Differences in physiological adaptation of Haberlea rhodopensis Friv. leaves and roots during dehydration–rehydration cycle
inferred← citeshttps://doi.org/10.1007/s11738-998-0010-8openalex-snapshot
Photosynthesis, respiration, and chlorophylls in presenescent, regreened, and senescent leaves of forest herb Smyrnium perfoliatum L. (Apiaceae)
inferred← citeshttps://doi.org/10.1007/s12298-013-0175-5openalex-snapshot
Chlorophyll fluorescence imaging of photosynthetic activity and pigment contents of the resurrection plants Ramonda serbica and Ramonda nathaliae during dehydration and rehydration
inferred← citeshttps://doi.org/10.1016/j.bbrep.2016.04.010openalex-snapshot
A method of water-soluble solid fraction saturation concentration evaluation in dry thalli of Antarctic lichenized fungi, in vivo
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2018.10.059openalex-snapshot
Low-temperature immobilization of water in Antarctic Turgidosculum complicatulum and in Prasiola crispa. Part I. Turgidosculum complicatulum
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.09.027openalex-snapshot
Chloroplast breakdown during dehydration of a homoiochlorophyllous resurrection plant proceeds via senescence-like processes
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104650openalex-snapshot
Physiological characterisation of tissue differentiation in response to desiccation in the homoiochlorophyllous dicot resurrection plant Craterostigma pumilum Hochst
inferred← citeshttps://doi.org/10.1016/j.flora.2006.12.004openalex-snapshot
Physiological ecology of photosynthesis of five sympatric species of Velloziaceae in the rupestrian fields of Serra do Cipó, Minas Gerais, Brazil
inferred← citeshttps://doi.org/10.1016/j.flora.2008.01.013openalex-snapshot
Marginal and laminar hydathode-like structures in the leaves of the desiccation-tolerant angiosperm Myrothamnus flabellifolius Welw.
inferred← citeshttps://doi.org/10.1016/j.jaridenv.2006.12.020openalex-snapshot
Anatomical, morphological and metabolic acclimation in the resurrection plant Reaumuria soongorica during dehydration and rehydration
inferred← citeshttps://doi.org/10.1016/j.jksus.2020.10.010openalex-snapshot
Optimization of regeneration and Agrobacterium tumefaciens-mediated transient transformation systems for Australian native extremophile, Tripogon loliiformis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2010.10.020openalex-snapshot
Proteome analysis of leaves of the desiccation-tolerant grass, Sporobolus stapfianus, in response to dehydration
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.12.016openalex-snapshot
Metabolomics as a complement to phylogenetics for assessing intraspecific boundaries in the desiccation-tolerant medicinal shrub Myrothamnus flabellifolia (Myrothamnaceae)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112323openalex-snapshot
The phenolic profile extracted from the desiccation-tolerant medicinal shrub Myrothamnus flabellifolia using Natural Deep Eutectic Solvents varies according to the solvation conditions
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.11.012openalex-snapshot
Unraveling metabolic mechanisms behind chloroplast desiccation tolerance: Chlorophyllous fern spore as a new promising unicellular model
inferred← citeshttps://doi.org/10.1016/j.sajb.2018.07.030openalex-snapshot
Different morpho-anatomical strategies against desiccation in five species of Xerophyta genus in relation to their ecophysiological aspects
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.09.003openalex-snapshot
Field and acclimated metabolomes of a resurrection plant suggest strong environmental regulation in the extreme end of the species’ range
inferred← citeshttps://doi.org/10.1016/s0065-2113(08)60182-0openalex-snapshot
Advances in Drought Tolerance in Plants
inferred← citeshttps://doi.org/10.1016/s0176-1617(11)80115-xopenalex-snapshot
Regreening of Desiccated Leaves of the Poikilochlorophyllous Xerophyta scabrida upon Rehydration
inferred← citeshttps://doi.org/10.1016/s0176-1617(11)81000-xopenalex-snapshot
Physiological Changes in Higher Poikilohydric Plants - Haberlea Rhodopensis Friv. and Ramonda Serbica Pan
inferred← citeshttps://doi.org/10.1016/s0176-1617(96)80263-xopenalex-snapshot
Reconstitution of Photosynthesis Upon Rehydration in the Desiccated Leaves of the Poikilochlorophyllous Shrub Xerophyta scabrida at Elevated CO2
inferred← citeshttps://doi.org/10.1016/s0176-1617(98)80275-7openalex-snapshot
Changes in laser-induced chlorophyll fluorescence ratio F690/F735 in the poikilochlorophyllous desiccation tolerant plant Xerophyta scabrida during desiccation
inferred← citeshttps://doi.org/10.1016/s0367-2530(17)30054-3openalex-snapshot
Survival strategies under extreme and complex environmental conditions: The aquatic resurrection plant Chamaegigas intrepidus
inferred← citeshttps://doi.org/10.1017/s026972700001410xopenalex-snapshot
Intracellular membranes: kinetics of superoxide production and changes in thylakoids of resurrection plants upon dehydration and rehydration
inferred← citeshttps://doi.org/10.1017/s0954102008001363openalex-snapshot
Deep dehydration ofUmbilicaria aprinathalli observed by proton NMR and sorption isotherm
inferred← citeshttps://doi.org/10.1017/s0954102012000041openalex-snapshot
Bound water freezing in AntarcticUmbilicaria aprinafrom Schirmacher Oasis
inferred← citeshttps://doi.org/10.1017/s1473550407003783openalex-snapshot
Adaptations to environmental extremes by multicellular organisms
inferred← citeshttps://doi.org/10.1023/a:1002619216027openalex-snapshot
Gas Exchange and Malate Accumulation in Haberlea Rhodopensis Grown Under Different Irradiances
inferred← citeshttps://doi.org/10.1023/a:1005927629018openalex-snapshot
Contents of sugars in leaves of drying desiccation tolerant flowering plants, particularly grasses
inferred← citeshttps://doi.org/10.1023/a:1005951908229openalex-snapshot
Ecophysiological responses of homoiochlorophyllous and poikilochlorophyllous desiccation tolerant plants: a comparison and an ecological perspective
inferred← citeshttps://doi.org/10.1023/a:1010692632408openalex-snapshot
Photosystem II photochemical efficiency, zeaxanthin and antioxidant contents in the poikilohydric Ramonda serbica during dehydration and rehydration
inferred← citeshttps://doi.org/10.1023/a:1014425619913openalex-snapshot
Some physiological comparisons between the resurrection grass, Eragrostis nindensis, and the related desiccation-sensitive species, E. curvula
inferred← citeshttps://doi.org/10.1023/a:1014473503075openalex-snapshot
Longevity of dry Myrothamnus flabellifolius in simulated field conditions
inferred← citeshttps://doi.org/10.1023/a:1026513800380openalex-snapshot
The discovery, scope, and puzzle of desiccation tolerance in plants
inferred← citeshttps://doi.org/10.1023/a:1026550808557openalex-snapshot
The evolution of vegetative desiccation tolerance in land plants
inferred← citeshttps://doi.org/10.1023/a:1026565817218openalex-snapshot
Granitic and gneissic outcrops (inselbergs) as centers of diversity for desiccation-tolerant vascular plants
inferred← citeshttps://doi.org/10.1034/j.1399-3054.1996.970420.xopenalex-snapshot
Desiccation tolerance in vegetative plant cells
inferred← citeshttps://doi.org/10.1038/s41598-021-86559-7openalex-snapshot
Stachyose triggers apoptotic like cell death in drought sensitive but not resilient plants
inferred← citeshttps://doi.org/10.1038/s41598-023-47456-3openalex-snapshot
Tripogon loliiformis tolerates rapid desiccation after metabolic and transcriptional priming during initial drying
inferred← citeshttps://doi.org/10.1046/j.1365-2435.1998.00173.xopenalex-snapshot
Carbon gains by desiccation‐tolerant plants at elevated CO2
inferred← citeshttps://doi.org/10.1046/j.1469-8137.1998.00104.xopenalex-snapshot
Initial stages of lichen hydration observed by proton magnetic relaxation
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2000.00755.xopenalex-snapshot
Xylem conduits of a resurrection plant contain a unique lipid lining and refill following a distinct pattern after desiccation
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2000.00759.xopenalex-snapshot
Water rise kinetics in refilling xylem after desiccation in a resurrection plant
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2002.00526.xopenalex-snapshot
Poikilohydry and homoihydry: antithesis or spectrum of possibilities?
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2003.00814.xopenalex-snapshot
The impact of lipid distribution, composition and mobility on xylem water refilling of the resurrection plantMyrothamnus flabellifolia
inferred← citeshttps://doi.org/10.1071/bt06172openalex-snapshot
Desiccation-induced ultrastructural and biochemical changes in the leaves of the resurrection plant Myrothamnus flabellifolia
inferred← citeshttps://doi.org/10.1071/bt9780485openalex-snapshot
The Occurrence of Resurrection Plants in the Australian Flora
inferred← citeshttps://doi.org/10.1071/bt9830085openalex-snapshot
Storage reserves of the seed-like, aestivating organs of Geophytes inhabiting granite outcrops in south-western Australia.
inferred← citeshttps://doi.org/10.1071/fp03167openalex-snapshot
Chlorophyll fluorescence of submerged and floating leaves of the aquatic resurrection plant Chamaegigas intrepidus
inferred← citeshttps://doi.org/10.1071/fp07087openalex-snapshot
Patterns of morphological leaf traits among pteridophytes along humidity and temperature gradients in the Bolivian Andes
inferred← citeshttps://doi.org/10.1071/fp08166openalex-snapshot
Sporobolus stapfianus, a model desiccation-tolerant grass
inferred← citeshttps://doi.org/10.1071/fp12321openalex-snapshot
The evolution of desiccation tolerance in angiosperm plants: a rare yet common phenomenon
inferred← citeshttps://doi.org/10.1071/pp96073openalex-snapshot
Changes in Gene Expression during Drying in a Desiccation-Tolerant Grass Sporobolus stapfianus and a Desiccation-Sensitive Grass Sporobolus pyramidalis
inferred← citeshttps://doi.org/10.1071/pp9820587openalex-snapshot
Humidity-sensitive Degreening and Regreening of Leaves of Borya nitida Labill. As Followed by Changes in Chlorophyll Fluorescence
inferred← citeshttps://doi.org/10.1078/0367-2530-00018openalex-snapshot
Structural and ultrastructural characterization of Selaginella lepidophylla, a desiccation-tolerant plant, during the rehydration process
inferred← citeshttps://doi.org/10.1080/00725560.1983.9648996openalex-snapshot
Growth analysis and photosynthetic rates in three selected grass species in theburkea‐eragrostissavanna
inferred← citeshttps://doi.org/10.1080/17550874.2024.2328832openalex-snapshot
Rethinking the relationship between desiccation-tolerant vascular plants and water deficit
inferred← citeshttps://doi.org/10.1086/297261openalex-snapshot
Physiological Aspects of Desiccation Tolerance-A Retrospect
inferred← citeshttps://doi.org/10.1086/337792openalex-snapshot
The Response of Bouteloua scorpioides to Water Stress at Two Phenological Stages
inferred← citeshttps://doi.org/10.1093/aob/mcad005openalex-snapshot
Demystifying the convergent ecological specialization of desiccation-tolerant vascular plants for water deficit
inferred← citeshttps://doi.org/10.1093/aob/mcy063openalex-snapshot
Accelerated diversification and functional trait evolution in Velloziaceae reveal new insights into the origins of the campos rupestres’ exceptional floristic richness
inferred← citeshttps://doi.org/10.1093/botlinnean/boab102openalex-snapshot
Recent divergence in functional traits affects rates of speciation in the Neotropical Velloziaceae (Pandanales)
inferred← citeshttps://doi.org/10.1093/icb/45.5.771openalex-snapshot
The Signature of Seeds in Resurrection Plants: A Molecular and Physiological Comparison of Desiccation Tolerance in Seeds and Vegetative Tissues
inferred← citeshttps://doi.org/10.1093/jxb/33.2.332openalex-snapshot
Protein Synthesis in the Desiccation Tolerant AngiospermXerophyta villosaduring Dehydration
inferred← citeshttps://doi.org/10.1093/jxb/35.9.1350openalex-snapshot
Abscisic Acid Content and Effects During Dehydration of Detached Leaves of Desiccation Tolerant Plants
inferred← citeshttps://doi.org/10.1093/jxb/44.5.921openalex-snapshot
Characterization of Protein Synthetic Changes in a Desiccation-Tolerant Fern,Polypodium virginianum. Comparison of the Effects of Drying, Rehydration and Abscisic Acid
inferred← citeshttps://doi.org/10.1093/jxb/48.6.1269openalex-snapshot
Desiccation-tolerantSporobolus stapfianus: lipid composition and cellular ultrastructure during dehydration and rehydration
inferred← citeshttps://doi.org/10.1093/jxb/erab022openalex-snapshot
Resurrection plants optimize photosynthesis despite very thick cell walls by means of chloroplast distribution
inferred← citeshttps://doi.org/10.1093/jxb/erab051openalex-snapshot
Natural ultraviolet radiation exposure alters photosynthetic biology and improves recovery from desiccation in a desert moss
inferred← citeshttps://doi.org/10.1093/jxb/erac104openalex-snapshot
When time is not of the essence: constraints to the carbon balance of bryophytes
inferred← citeshttps://doi.org/10.1093/jxb/erf028openalex-snapshot
Recovery of the resurrection plant Craterostigma wilmsii from desiccation: protection versus repair
inferred← citeshttps://doi.org/10.1093/jxb/ern226openalex-snapshot
Expression of Xhdsi-1VOC, a novel member of the vicinal oxygen chelate (VOC) metalloenzyme superfamily, is up-regulated in leaves and roots during desiccation in the resurrection plant Xerophyta humilis (Bak) Dur and Schinz
inferred← citeshttps://doi.org/10.1093/jxb/erx489openalex-snapshot
Molecular responses to dehydration and desiccation in desiccation-tolerant angiosperm plants
inferred← citeshttps://doi.org/10.1093/jxb/erz472openalex-snapshot
Positive root pressure is critical for whole-plant desiccation recovery in two species of terrestrial resurrection ferns
inferred← citeshttps://doi.org/10.1101/2022.09.14.508022openalex-snapshot
Ultraviolet radiation and dehydration stress induce overlapping transcriptional and metabolic responses in Syntrichia mosses
inferred← citeshttps://doi.org/10.1104/pp.106.077701openalex-snapshot
Response of the Leaf Cell Wall to Desiccation in the Resurrection Plant Myrothamnus flabellifolius
inferred← citeshttps://doi.org/10.1104/pp.97.4.1501openalex-snapshot
Influence of Protoplasmic Water Loss on the Control of Protein Synthesis in the Desiccation-Tolerant Moss Tortula ruralis
inferred← citeshttps://doi.org/10.1111/1365-2435.12462openalex-snapshot
Carbon assimilation and habitat segregation in resurrection plants: a comparison between desiccation‐ and non‐desiccation‐tolerant species of Neotropical Velloziaceae (Pandanales)
inferred← citeshttps://doi.org/10.1111/boj.12018openalex-snapshot
A revision of African Velloziaceae based on leaf anatomy characters andrbcLnucleotide sequences
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2004.01212.xopenalex-snapshot
Insights into the cellular mechanisms of desiccation tolerance among angiosperm resurrection plant species
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2008.03673.xopenalex-snapshot
Desiccation tolerance in the vegetative tissues of the fern Mohria caffrorum is seasonally regulated
inferred← citeshttps://doi.org/10.1111/j.1399-3054.1996.tb00448.xopenalex-snapshot
Loss of chlorophylls, cessation of photosynthetic CO2 assimilation and respiration in the poikilochlorophyllous plant Xerophyta scabrida during desiccation
inferred← citeshttps://doi.org/10.1111/j.1469-8137.1996.tb01902.xopenalex-snapshot
Photosynthetic responses of a moss, Tortula ruralis , ssp. ruralis , and the lichens Cladonia convoluta and C. furcata to water deficit and short periods of desiccation, and their ecophysiological significance: a baseline study at present‐day CO 2 concentration
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2004.01306.xopenalex-snapshot
Seasonal adaptations of the tuberous roots of Ranunculus asiaticus to desiccation and resurrection by changes in cell structure and protein content
inferred← citeshttps://doi.org/10.1111/jbi.15048openalex-snapshot
Similar, but Not the Same: Time and Mode of Climatic Niche Evolution in a Highly Endemic Lineage
inferred← citeshttps://doi.org/10.1111/njb.03939openalex-snapshot
Desiccation‐tolerant vascular plants from Western Ghats, India: review, updated checklist, future prospects and new insights
inferred← citeshttps://doi.org/10.1111/nph.16067openalex-snapshot
High‐resolution computed tomography reveals dynamics of desiccation and rehydration in fern petioles of a desiccation‐tolerant fern
inferred← citeshttps://doi.org/10.1111/nph.17445openalex-snapshot
Differences in biochemical, gas exchange and hydraulic response to water stress in desiccation tolerant and sensitive fronds of the fern Anemia caffrorum
inferred← citeshttps://doi.org/10.1111/nph.19719openalex-snapshot
Resurrection plants revisited: bridging the gap between bryophytes and angiosperms to decode desiccation tolerance
inferred← citeshttps://doi.org/10.1111/nph.71466openalex-snapshot
Desiccation tolerance mechanisms in the green lineage and beyond
inferred← citeshttps://doi.org/10.1111/ppl.12890openalex-snapshot
A field portable method for the semi‐quantitative estimation of dehydration tolerance of photosynthetic tissues across distantly related land plants
inferred← citeshttps://doi.org/10.1111/tpj.13227openalex-snapshot
Protection of the photosynthetic apparatus against dehydration stress in the resurrection plant Craterostigma pumilum
inferred← citeshttps://doi.org/10.1127/0340-269x/2005/0035-0449openalex-snapshot
Ephemeral pools as stressful and isolated habitats for the endemic aquatic resurrection plant Chamaegigas intrepidus
inferred← citeshttps://doi.org/10.1139/b92-015openalex-snapshot
Effects of dehydration and rehydration on the polar lipid and fatty acid composition of Ramonda species
inferred← citeshttps://doi.org/10.1139/b94-222openalex-snapshot
Direct absorption of water by hairy leaves of Phlomis fruticosa and its contribution to drought avoidance
inferred← citeshttps://doi.org/10.1146/annurev.pp.30.060179.001211openalex-snapshot
Physiological Aspects of Desiccation Tolerance
inferred← citeshttps://doi.org/10.11606/d.41.2012.tde-21012013-141040openalex-snapshot
Microgramma squamulosa (Kaulf.) de la Sota e Pleopeltis hirsutissima (Raddi) de la Sota: estratégias contrastantes de uso da água em um ambiente epifítico
inferred← citeshttps://doi.org/10.11606/t.11.2010.tde-22052013-150802openalex-snapshot
Implicações da manutenção ou perda da clorofila na tolerância à dessecação de tecidos vegetativos de Anemia flexuosa (Schizaeaceae) e Pleurostima purpurea (Velloziaceae)
inferred← citeshttps://doi.org/10.1163/2031356x-00704005openalex-snapshot
Plant Ecology of the Namib Desert
inferred← citeshttps://doi.org/10.1179/jbr.1988.15.1.219openalex-snapshot
Survival of a desiccation-tolerant moss, Grimmia laevigata, beyond its observed microdistributional limits
inferred← citeshttps://doi.org/10.1201/9780824746728.ch10openalex-snapshot
Plant Response to Water-Deficit Conditions
inferred← citeshttps://doi.org/10.1201/9781420007626-2openalex-snapshot
Opportunistic Growth and Desiccation Tolerance: The Ecological Success of Poikilohydrous Autotrophs
inferred← citeshttps://doi.org/10.1201/9781420007626.ch2openalex-snapshot
Opportunistic Growth and Desiccation Tolerance
inferred← citeshttps://doi.org/10.12693/aphyspola.109.389openalex-snapshot
The Effect of Water Accessible Paramagnetic Ions on Subcellular Structures Formed in Developing Wheat Photosynthetic Membranes as Observed by NMR and by Sorption Isotherm
inferred← citeshttps://doi.org/10.12693/aphyspola.109.411openalex-snapshot
Bound Water Structure on the Surfaces of Usnea antarctica as Observed by NMR and Sorption Isotherm
inferred← citeshttps://doi.org/10.12693/aphyspola.115.516openalex-snapshot
Deep Dehydration of Antarctic Lichen Leptogium puberulum Hue Observed by NMR and Sorption Isotherm
inferred← citeshttps://doi.org/10.12693/aphyspola.115.521openalex-snapshot
Rehydration of Digalactosyldiacylglycerol Model Membrane Lyophilizates Observed by NMR and Sorption Isotherm
inferred← citeshttps://doi.org/10.12693/aphyspola.115.526openalex-snapshot
Maturation Process of Photosynthetic Membranes Observed by Proton Magnetic Relaxation and Sorption Isotherm
inferred← citeshttps://doi.org/10.12693/aphyspola.121.480openalex-snapshot
Initial Phases of Antarctic Ramalina terebrata Hook f. & Taylor Thalli Rehydration Observed by Proton Relaxometry
inferred← citeshttps://doi.org/10.12693/aphyspola.121.491openalex-snapshot
Water Bound in Elytra of the Weevil Liparus glabrirostris (Küster, 1849) by NMR and Sorption Isotherm (Coleoptera: Curculionidae)
inferred← citeshttps://doi.org/10.12693/aphyspola.129.179openalex-snapshot
The Effect of Mild Rehydration on Freeze-Dried Dipalmitoylphosphatidylcholine (DPPC) Multilamellar Membranes as Observed by Proton NMR and Sorption Isotherm
inferred← citeshttps://doi.org/10.12775/eq.2024.039openalex-snapshot
Effect of light stress on maximum photochemical efficiency of photosystem II and chloroplast structure in cryptogams Cladonia mitis and Pleurozium schreberi
inferred← citeshttps://doi.org/10.1515/cmble-2015-0040openalex-snapshot
Non-cooperative immobilization of residual water bound in lyophilized photosynthetic lamellae
inferred← citeshttps://doi.org/10.1590/2175-7860200758114openalex-snapshot
Diversidade em quatro áreas de campos rupestres na Chapada Diamantina, Bahia, Brasil: espécies distintas, mas riquezas similares
inferred← citeshttps://doi.org/10.1590/s0100-84042007000300012openalex-snapshot
Reproductive phenology, pollination and seed dispersal syndromes on sandstone outcrop vegetation in the "Chapada Diamantina", northeastern Brazil: population and community analyses
inferred← citeshttps://doi.org/10.1590/s0102-33062007000200008openalex-snapshot
Ilhas de vegetação em afloramentos de quartzito-arenito no Morro do Pai Inácio, Chapada Diamantina, Bahia, Brasil
inferred← citeshttps://doi.org/10.1590/s1676-06032011000200026openalex-snapshot
Life-form spectra of quartzite and itabirite rocky outcrop sites, Minas Gerais, Brazil
inferred← citeshttps://doi.org/10.1640/0002-8444(2007)97[175:dareol]2.0.co;2openalex-snapshot
Desiccation and Rehydration Experiments on Leaves of 43 Pteridophyte Species
inferred← citeshttps://doi.org/10.17760/d20000057openalex-snapshot
Mechanism for differential desiccation tolerance in porphyra species
inferred← citeshttps://doi.org/10.18174/465557openalex-snapshot
Unfolding plant desiccation tolerance : evolution, structure, and function of LEA proteins
inferred← citeshttps://doi.org/10.2139/ssrn.5175178openalex-snapshot
Trait Combinations Determine the Ability of Desiccation Tolerant Plants to Tolerate Desiccation
inferred← citeshttps://doi.org/10.21825/af.v7i4.5854openalex-snapshot
Plant Ecology of the Namib Desert
inferred← citeshttps://doi.org/10.22541/au.159493223.30789439openalex-snapshot
UV tolerance and sustained non-photochemical quenching in a desert moss
inferred← citeshttps://doi.org/10.2307/1554963openalex-snapshot
Xerophyta seinei (Velloziaceae), a distinctive new species from Zimbabwe
inferred← citeshttps://doi.org/10.2307/2425790openalex-snapshot
Comparative Desiccation Tolerance of Three Desert Pteridophytes: Response to Long-term Desiccation
inferred← citeshttps://doi.org/10.2307/3546626openalex-snapshot
The Effect of Density on Size Frequency Distributions in Chalk Grassland Bryophyte Populations
inferred← citeshttps://doi.org/10.23880/ijbp-16000131openalex-snapshot
Resurrection of the Fern "Cheilanthes albomarginata Clarke" Involves Utilization of Trehalose as Energy Source and Accumulation of Protective Stress Metabolites
inferred← citeshttps://doi.org/10.3120/0024-9637-71.4.145openalex-snapshot
UNVEILING NATURE'S SUNSCREEN: THE POTENTIAL ROLE OF LIVERWORT SCALES IN UV PROTECTION
inferred← citeshttps://doi.org/10.3389/fpls.2018.00543openalex-snapshot
Plant Life in Extreme Environments: How Do You Improve Drought Tolerance?
inferred← citeshttps://doi.org/10.3389/fpls.2019.01396openalex-snapshot
Desiccation-Driven Senescence in the Resurrection Plant Xerophyta schlechteri (Baker) N.L. Menezes: Comparison of Anatomical, Ultrastructural, and Metabolic Responses Between Senescent and Non-Senescent Tissues
inferred← citeshttps://doi.org/10.3390/agronomy8080146openalex-snapshot
Plant Desiccation Tolerance and its Regulation in the Foliage of Resurrection “Flowering-Plant” Species
inferred← citeshttps://doi.org/10.3390/molecules24071240openalex-snapshot
Metabolomic Profiling of the Desiccation-Tolerant Medicinal Shrub Myrothamnus flabellifolia Indicates Phenolic Variability Across Its Natural Habitat: Implications for Tea and Cosmetics Production
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