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Membranes and organelles of dehydratedSelaginella andTortula retain their normal configuration and structural integrity
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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.tb13299.xopenalex-snapshot
ULTRASTRUCTURAL CHANGES OF MEMBRANES WITH HYDRATION IN SOYBEAN SEEDS
inferredcites →https://doi.org/10.1002/j.1537-2197.1993.tb13779.xopenalex-snapshot
COMPARATIVE MEASURES OF DESICCATION‐TOLERANCE IN THE TORTULA RURALIS COMPLEX. I. VARIATION IN DAMAGE CONTROL AND REPAIR
inferredcites →https://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
inferredcites →https://doi.org/10.1007/bf00202321openalex-snapshot
Molecular cloning of abscisic acid-modulated genes which are induced during desiccation of the resurrection plant Craterostigma plantagineum
inferredcites →https://doi.org/10.1007/bf00392352openalex-snapshot
Freeze-fracture observations on membranes of dry and hydrated pollen from Collomia, Phoenix and Zea
inferredcites →https://doi.org/10.1007/bf00397900openalex-snapshot
Ultrastructure of barley aleurone cells as shown by freeze-etching
inferredcites →https://doi.org/10.1007/bf00762213openalex-snapshot
Phase transitions and permeability changes in dry membranes during rehydration
inferredcites →https://doi.org/10.1007/bf01279914openalex-snapshot
Structure of plasma membrane in radicles from cotton seeds
inferredcites →https://doi.org/10.1007/bf01354000openalex-snapshot
In dry pear (Pyrus communis L.) pollen, membranes assume a tightly packed multilamellate aspect that disappears rapidly upon hydration
inferredcites →https://doi.org/10.1016/0005-2736(70)90060-xopenalex-snapshot
Lamellar and hexagonal lipid phases visualized by freeze-etching
inferredcites →https://doi.org/10.1016/0009-3084(86)90067-8openalex-snapshot
Lipid polymorphism and the roles of lipids in membranes
inferredcites →https://doi.org/10.1016/0014-5793(84)80077-0openalex-snapshot
Membrane Fluidity in Biology. Vol. 1. Concepts of Membrane Structure
inferredcites →https://doi.org/10.1016/0302-4598(85)80031-3openalex-snapshot
Biological Membranes. Vol. 5.
inferredcites →https://doi.org/10.1016/0304-4157(88)90015-9openalex-snapshot
Interactions of sugars with membranes
inferredcites →https://doi.org/10.1016/b978-0-12-053001-4.50006-9openalex-snapshot
Structural Properties of Lipids and Their Functional Roles in Biological Membranes
inferredcites →https://doi.org/10.1016/b978-0-12-198080-1.50014-4openalex-snapshot
MEMBRANES IN DRY AND IMBIBING SEEDS
inferredcites →https://doi.org/10.1016/s0021-9258(18)63891-8openalex-snapshot
Novel Water Stress Protein from a Desiccation-tolerant Cyanobacterium
inferredcites →https://doi.org/10.1016/s0022-5320(82)80002-6openalex-snapshot
Ultrastructural and biochemical bases of resurrection in the drought-tolerant vascular plant, Selaginella lepidophylla
inferredcites →https://doi.org/10.1080/00021369.1988.10869128openalex-snapshot
Analysis of Physical States of Water in Soybean Seeds by NMR
inferredcites →https://doi.org/10.1083/jcb.12.2.207openalex-snapshot
THE STRUCTURE OF THE LIQUID-CRYSTALLINE PHASES OF LIPID-WATER SYSTEMS
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a087030openalex-snapshot
The Fine Structure of some Dry Seed Tissues Observed after Completely Anhydrous Chemical Fixation
inferredcites →https://doi.org/10.1104/pp.69.1.135openalex-snapshot
Protein Synthesis and Photosynthetic Recovery in the Resurrection Plant, Selaginella lepidophylla
inferredcites →https://doi.org/10.1104/pp.74.4.923openalex-snapshot
Plant Desiccation and Protein Synthesis
inferredcites →https://doi.org/10.1104/pp.75.4.1075openalex-snapshot
Membrane Organization of the Desiccation-Tolerant Moss Tortula ruralis in Dehydrated States
inferredcites →https://doi.org/10.1104/pp.83.4.761openalex-snapshot
Plasma Membrane Lipid Alterations Associated with Cold Acclimation of Winter Rye Seedlings (Secale cereale L. cv Puma)
inferredcites →https://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
inferredcites →https://doi.org/10.1105/tpc.2.6.503openalex-snapshot
Gene Expression in Response to Abscisic Acid and Osmotic Stress
inferredcites →https://doi.org/10.1111/1365-3040.ep11592139openalex-snapshot
Changes in plasmalemma organization in cowpea radicle during imbibition in water and NaCl solutions
inferredcites →https://doi.org/10.1111/j.1365-3040.1982.tb00936.xopenalex-snapshot
Ultrastructure and membrane permeability in cowpea seeds
inferredcites →https://doi.org/10.1111/j.1469-8137.1974.tb02118.xopenalex-snapshot
PHOSPHOLIPIDS AND PLANT MEMBRANE PERMEABILITY
inferredcites →https://doi.org/10.1111/j.1469-8137.1978.tb01640.xopenalex-snapshot
REGENERATION OF CHLOROPLAST STRUCTURE IN TALBOTIA ELEGANS: A DESICCATION‐TOLERANT PLANT
inferredcites →https://doi.org/10.1111/j.1469-8137.1978.tb02640.xopenalex-snapshot
RE‐ORGANIZATION OF FINE STRUCTURE DURING REHYDRATION OF DESICCATED LEAVES OF XEROPHYTA VILLOSA
inferredcites →https://doi.org/10.1111/j.1469-8137.1979.tb07565.xopenalex-snapshot
DESICCATION EFFECTS AND CATION DISTRIBUTION IN BRYOPHYTES
inferredcites →https://doi.org/10.1111/j.1469-8137.1979.tb07575.xopenalex-snapshot
ULTRASTRUCTURE OF DRY SEED TISSUE AFTER A NON‐AQUEOUS PRIMARY FIXATION
inferredcites →https://doi.org/10.1111/j.1469-8137.1980.tb00767.xopenalex-snapshot
THE ULTRASTRUCTURE OF COLEOPTILE CELLS IN DRY RICE (ORYZA SATIVA L.) GRAINS AFTER ANHYDROUS FIXATION WITH OSMIUM TETROXIDE VAPOUR
inferredcites →https://doi.org/10.1111/j.1469-8137.1991.tb01050.xopenalex-snapshot
Studies on the anhydrous fixation of dry seeds of lettuce (Lactuca saliva L.)
inferredcites →https://doi.org/10.1139/b81-320openalex-snapshot
Responses of the moss Tortula ruralis to desiccation treatments. I. Effects of minimum water content and rates of dehydration and rehydration
inferredcites →https://doi.org/10.1146/annurev.pp.30.060179.001211openalex-snapshot
Physiological Aspects of Desiccation Tolerance
inferredcites →https://doi.org/10.3109/10520298209066734openalex-snapshot
Freeze Fracture of Intact Plant Tissues
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.24917/25438832.5.9zenodo-depositor-declared
Impact of water stress on physiological processes of moss Polytrichum piliferum Hedw.
inferred← citeshttps://doi.org/10.1002/9780470376881.ch2openalex-snapshot
Lessons on Dehydration Tolerance from Desiccation‐Tolerant Plants
inferred← citeshttps://doi.org/10.1002/9780470650608.ch3openalex-snapshot
Desiccation‐Tolerance of Plant Tissues: A Mechanistic Overview
inferred← citeshttps://doi.org/10.1006/anbo.1996.0375openalex-snapshot
Conservation of Cell Order in Desiccated Mesophyll ofSelaginella lepidophylla([Hook and Grev.] Spring)
inferred← citeshttps://doi.org/10.1006/anbo.1997.0476openalex-snapshot
Importance of the Fixative for Reliable Ultrastructural Preservation of Poikilohydric Plant Tissues. Observations on Dry, Partially, and Fully Hydrated Tissues ofSelaginella lepidophylla
inferred← citeshttps://doi.org/10.1007/978-0-306-48568-8_5openalex-snapshot
Molecular Biology and Genomics of the Desiccation Tolerant Moss Tortula Ruralis
inferred← citeshttps://doi.org/10.1007/978-1-4020-6285-8_16openalex-snapshot
Desiccation-tolerant plants in dry environments
inferred← citeshttps://doi.org/10.1007/978-1-4899-0069-2_1openalex-snapshot
Desiccation Tolerance in Mosses
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/10.1007/978-981-13-1244-1_10openalex-snapshot
Mechanisms Underlying Freezing and Desiccation Tolerance in Bryophytes
inferred← citeshttps://doi.org/10.1007/bf01306605openalex-snapshot
Freeze-substitution of dehydrated plant tissues: Artefacts of aqueous fixation revisited
inferred← citeshttps://doi.org/10.1007/s11099-011-0002-6openalex-snapshot
Photosynthetic and cytological recovery on remoistening Syntrichia caninervis Mitt., a desiccation-tolerant moss from Northwestern China
inferred← citeshttps://doi.org/10.1007/s11157-006-0015-yopenalex-snapshot
Desiccation-tolerant plants in dry environments
inferred← citeshttps://doi.org/10.1007/s11738-017-2454-1openalex-snapshot
Desiccation-related responses of antioxidative enzymes and photosynthetic pigments in Brachythecium procumbens (Mitt.) A. Jaeger
inferred← citeshttps://doi.org/10.1007/s11738-997-0038-1openalex-snapshot
How some plants recover from vegetative desiccation: A repair based strategy
inferred← citeshttps://doi.org/10.1007/s40502-020-00530-8openalex-snapshot
An adaptive inducible ecological tolerance strategy of Semibarbula orientalis (Web.) Wijk. & Marg. to desiccation stress
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.150981openalex-snapshot
Remodeling of membrane lipids associated with ABA-induced desiccation tolerance in Physcomitrium patens
inferred← citeshttps://doi.org/10.1016/j.jplph.2010.05.028openalex-snapshot
Reorganization of photosystem II is involved in the rapid photosynthetic recovery of desert moss Syntrichia caninervis upon rehydration
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.plaphy.2024.108620openalex-snapshot
Autophagy functions as a cytoprotective mechanism by regulating programmed cell death during desiccation in Syntrichia caninervis
inferred← citeshttps://doi.org/10.1016/j.ppees.2019.02.004openalex-snapshot
Genetic and expression differences between putative ecotypes of Sphagnum denticulatum Brid. (Sphagnaceae: Bryophyta) subjected to drought stress and rehydration
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2008.12.005openalex-snapshot
The effects of drying following heat shock exposure of the desert moss Syntrichia caninervis
inferred← citeshttps://doi.org/10.1016/s0981-9428(00)01214-6openalex-snapshot
The effect of desiccation and rehydration on the integrityof small subunit ribosomal RNAs in desiccation tolerantand intolerant plants
inferred← citeshttps://doi.org/10.1023/a:1005863015130openalex-snapshot
“To dryness and beyond” – Preparation for the dried state and rehydration in vegetative desiccation-tolerant 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:1026598724487openalex-snapshot
Bryophytes as experimental models for the study of environmental stress tolerance: Tortula ruralis and desiccation-tolerance in mosses
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/s41598-020-69080-1openalex-snapshot
Exogenous abscisic acid induces the lipid and flavonoid metabolism of tea plants under drought stress
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2002.00517.xopenalex-snapshot
Abscisic acid modifies the changes in lipids brought about by water stress in the moss Atrichum androgynum
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/10.1079/ssr2004161openalex-snapshot
Cold-induced imbibition damage of lettuce embryos: a study using cryo-scanning electron microscopy
inferred← citeshttps://doi.org/10.1080/15592324.2019.1621089openalex-snapshot
The effects of environmental light on the reorganization of chloroplasts in the resurrection of Selaginella tamariscina
inferred← citeshttps://doi.org/10.1086/595285openalex-snapshot
Effects of De‐ and Rehydration in Desiccation‐Tolerant Liverworts: A Cytological and Physiological Study
inferred← citeshttps://doi.org/10.1093/aob/mcl092openalex-snapshot
Effects of De- and Rehydration on Food-conducting Cells in the Moss Polytrichum formosum: A Cytological Study
inferred← citeshttps://doi.org/10.1093/aob/mcl246openalex-snapshot
Desiccation Tolerance in the Moss Polytrichum formosum: Physiological and Fine-structural Changes during Desiccation and Recovery
inferred← citeshttps://doi.org/10.1093/icb/45.5.788openalex-snapshot
Desiccation Tolerance in Bryophytes: A Reflection of the Primitive Strategy for Plant Survival in Dehydrating Habitats?
inferred← citeshttps://doi.org/10.1093/jexbot/52.364.2105openalex-snapshot
Desiccation tolerance of protoplasts isolated from pea embryos
inferred← citeshttps://doi.org/10.1093/jexbot/53.371.1197openalex-snapshot
Two early light-inducible protein (ELIP) cDNAs from the resurrection plant Tortula ruralis are differentially expressed in response to desiccation, rehydration, salinity, and high light
inferred← citeshttps://doi.org/10.1093/jxb/45.5.577openalex-snapshot
Accumulation and polysomal recruitment of transcripts in response to desiccation and rehydration of the mossTortula ruralis
inferred← citeshttps://doi.org/10.1093/jxb/erac172openalex-snapshot
Desiccation–rehydration measurements in bryophytes: current status and future insights
inferred← citeshttps://doi.org/10.1093/jxb/ert145openalex-snapshot
Evidence for the absence of enzymatic reactions in the glassy state. A case study of xanthophyll cycle pigments in the desiccation-tolerant moss Syntrichia ruralis
inferred← citeshttps://doi.org/10.1093/mp/ssp018openalex-snapshot
Between a Rock and a Dry Place: The Water-Stressed Moss
inferred← citeshttps://doi.org/10.1098/rstb.2016.0498openalex-snapshot
The evolution of the stomatal apparatus: intercellular spaces and sporophyte water relations in bryophytes—two ignored dimensions
inferred← citeshttps://doi.org/10.1104/pp.114.255794openalex-snapshot
Photoprotection Conferred by Changes in Photosynthetic Protein Levels and Organization during Dehydration of a Homoiochlorophyllous Resurrection Plant
inferred← citeshttps://doi.org/10.1111/j.1399-3054.2009.01245.xopenalex-snapshot
A combined subtractive suppression hybridization and expression profiling strategy to identify novel desiccation response transcripts from Tortula ruralis gametophytes
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Altered Fatty Acid Profile of Polar Lipids in Maize Seedlings in Response to Excess Copper
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.1469-8137.2009.03148.xopenalex-snapshot
Cytological insights into the desiccation biology of a model system: moss protonemata
inferred← citeshttps://doi.org/10.1111/j.1744-7909.2007.00585.xopenalex-snapshot
Effects of Cadmium on Polar Lipid Composition and Unsaturation in Maize (Zea mays) in Hydroponic Culture
inferred← citeshttps://doi.org/10.1111/pce.12266openalex-snapshot
Differential proteomics of dehydration and rehydration in bryophytes: evidence towards a common desiccation tolerance mechanism
inferred← citeshttps://doi.org/10.1111/plb.12140openalex-snapshot
Physiological history may mask the inherent inducible desiccation tolerance strategy of the desert moss C rossidium crassinerve
inferred← citeshttps://doi.org/10.1111/ppl.12511openalex-snapshot
Dehydration rate determines the degree of membrane damage and desiccation tolerance in bryophytes
inferred← citeshttps://doi.org/10.1139/b96-091openalex-snapshot
CO2 exchange, photosynthetic pigment composition, and cell ultrastructure of Sphagnum mosses during dehydration and subsequent rehydration
inferred← citeshttps://doi.org/10.1155/2018/9464592openalex-snapshot
Perspectives on Structural, Physiological, Cellular, and Molecular Responses to Desiccation in Resurrection Plants
inferred← citeshttps://doi.org/10.1179/1743282011y.0000000043openalex-snapshot
Membrane stability of the desert mossSyntrichia caninervisMitt. during desiccation and rehydration
inferred← citeshttps://doi.org/10.1186/1471-2164-11-143openalex-snapshot
Chloroplast genome sequence of the moss Tortula ruralis: gene content, polymorphism, and structural arrangement relative to other green plant chloroplast genomes
inferred← citeshttps://doi.org/10.1186/1471-2164-5-89openalex-snapshot
The rehydration transcriptome of the desiccation-tolerant bryophyte Tortula ruralis: transcript classification and analysis
inferred← citeshttps://doi.org/10.1186/1756-0500-7-490openalex-snapshot
De novo assembly and characterization of the transcriptome in the desiccation-tolerant moss Syntrichia caninervis
inferred← citeshttps://doi.org/10.1201/9780824746728.ch10openalex-snapshot
Plant Response to Water-Deficit Conditions
inferred← citeshttps://doi.org/10.13057/biodiv/d190548openalex-snapshot
Predicting impacts of future climate change on the distribution of the widespread selaginellas (Selaginella ciliaris and S. plana) in Southeast Asia
inferred← citeshttps://doi.org/10.13057/biodiv/d211157openalex-snapshot
Anticipated climate changes reveal shifting in habitat suitability of high-altitude selaginellas in Java, Indonesia
inferred← citeshttps://doi.org/10.13057/nusbiosci/n030101openalex-snapshot
Optimization of DNA extraction of physic nut (Jatropha curcas) by selecting the appropriate leaf
inferred← citeshttps://doi.org/10.13057/nusbiosci/n030107openalex-snapshot
Review: Natural products from Genus Selaginella (Selaginellaceae)
inferred← citeshttps://doi.org/10.1556/abiol.60.2009.1.10openalex-snapshot
A comparative analysis of fatty acid composition of root and shoot lipids inZea maysunder copper and cadmium stress
inferred← citeshttps://doi.org/10.1639/0007-2745(2007)110[163:ienfib]2.0.co;2openalex-snapshot
The nature and distribution of vegetative desiccation-tolerance in hornworts, liverworts and mosses
inferred← citeshttps://doi.org/10.1639/0007-2745-117.2.110openalex-snapshot
Degradation and reorganization of thylakoid protein complexes ofBryum argenteumin response to dehydration and rehydration
inferred← citeshttps://doi.org/10.1639/0007-2745-120.2.129openalex-snapshot
Ecology of desiccation tolerance in bryophytes: A conceptual framework and methodology
inferred← citeshttps://doi.org/10.1639/0007-2745-120.2.130openalex-snapshot
Ecology of desiccation tolerance in bryophytes: A conceptual framework and methodology
inferred← citeshttps://doi.org/10.1639/0007-2745-121.2.193openalex-snapshot
The role of prehydration in rescuing shoots of mosses damaged by extreme desiccation events: Syntrichia norvegica (Pottiaceae)
inferred← citeshttps://doi.org/10.1639/0007-2745-125.4.602openalex-snapshot
Effects of desiccation rate and inhibition of protein synthesis and the violaxanthin cycle on the rewetting recovery of Porella platyphylla
inferred← citeshttps://doi.org/10.21406/abpa.2016.4.89openalex-snapshot
Light microscopic study of Porella platyphylla (L.) Pfeiff. cells under various abiotic stress factors
inferred← citeshttps://doi.org/10.3390/genes14020390openalex-snapshot
Proteomic and Transcriptomic Responses of the Desiccation-Tolerant Moss Racomitrium canescens in the Rapid Rehydration Processes
inferred← citeshttps://doi.org/10.3390/plants9111431openalex-snapshot
Exploratory Study of Fatty Acid Profile in Two Filmy Ferns with Contrasting Desiccation Tolerance Reveal the Production of Very Long Chain Polyunsaturated Omega-3 Fatty Acids
inferred← citeshttps://doi.org/10.35196/rfm.2004.1.17openalex-snapshot
ACTIVIDAD DE TREHALOSA 6-FOSFATO SINTASA EN PLANTAS DE Selaginella lepidophylla EN RESPUESTA A HIDRATACIÓN Y DESECACIÓN
inferred← citeshttps://doi.org/10.3923/ijar.2007.126.135openalex-snapshot
Changes in Polar Lipid Composition in Maize Seedlings Induced by Cadmium Stress
inferred← citeshttps://doi.org/10.5194/bg-15-797-2018openalex-snapshot
Effects of storage temperature on the physiological characteristics and vegetative propagation of desiccation-tolerant mosses
inferred← citeshttps://doi.org/10.5194/bg-22-6291-2025openalex-snapshot
Temperature-driven vapor pressure deficit structures forest bryophyte communities across the landscape
inferred← citeshttps://doi.org/10.54598/001200openalex-snapshot
Small-spatial scale ecophysiological and stress- induced (salicylic acid) biochemical investigations on desiccation-tolerant bryophyte SYNTRICHIA RURALIS
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