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Ice formation in the freeze-tolerant eutardigrades Adorybiotus coronifer and Amphibolus nebulosus studied by differential scanning calorimetry
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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/jez.1402580305openalex-snapshot
Trehalose accumulation in the tardigrade Adorybiotus coronifer during anhydrobiosis
inferredcites →https://doi.org/10.1007/978-1-4757-0190-6_2openalex-snapshot
Principles of Insect Low Temperature Tolerance
inferredcites →https://doi.org/10.1007/978-1-4757-0190-6_5openalex-snapshot
Hemolymph Proteins Involved in Insect Subzero-Temperature Tolerance: Ice Nucleators and Antifreeze Proteins
inferredcites →https://doi.org/10.1016/0011-2240(81)90104-8openalex-snapshot
Determination of water “bound” by soluble subcellular components during low-temperature acclimation in the gall fly larva, Eurosta solidagensis
inferredcites →https://doi.org/10.1016/0011-2240(82)90139-0openalex-snapshot
A method for quantitative determination of ice nucleating agents in insect hemolymph
inferredcites →https://doi.org/10.1016/0011-2240(90)90023-wopenalex-snapshot
Are freezing and dehydration similar stress vectors? A comparison of modes of interaction of stabilizing solutes with biomolecules
inferredcites →https://doi.org/10.1016/0011-2240(91)90044-oopenalex-snapshot
Tissue distribution of the ice-nucleating agents in larvae of the rice stem borer, Chilo suppressalis Walker (Lepidoptera: Pyralidae)
inferredcites →https://doi.org/10.1016/0011-2240(92)90012-qopenalex-snapshot
Survival of the cryptobiotic eutardigrade Adorybiotus coronifer during cooling to −196 °C: Effect of cooling rate, trehalose level, and short-term acclimation
inferredcites →https://doi.org/10.1016/0022-1910(85)90034-4openalex-snapshot
Freeze-tolerance adaptations, including haemolymph protein and lipoprotein nucleators, in the larvae of the cranefly Tipula trivittata
inferredcites →https://doi.org/10.1016/0022-1910(90)90116-wopenalex-snapshot
Ingestion of ice-nucleating active bacteria increases the supercooling point of the lady beetle Hippodamia convergens
inferredcites →https://doi.org/10.1016/0300-9629(79)90148-8openalex-snapshot
Osmotically inactive water in relation to tolerance to freezing in Eleodes blanchardi beetles
inferredcites →https://doi.org/10.1016/0300-9629(82)90268-7openalex-snapshot
Physiological adaptations to low temperature in freezing-tolerant Phyllodecta laticollis beetles
inferredcites →https://doi.org/10.1016/0300-9629(82)90269-9openalex-snapshot
The role of osmotic stress and surface energy in freezing injury of sea urchin eggs
inferredcites →https://doi.org/10.1016/0300-9629(91)90023-6openalex-snapshot
ICE-nucleating activity in the freeze-tolerant tardigrade Adorybiotus coronifer
inferredcites →https://doi.org/10.1016/0306-4565(90)90006-4openalex-snapshot
A simple moder for estimating the ice content of freezing ectotherms
inferredcites →https://doi.org/10.1016/0306-4565(91)90054-6openalex-snapshot
The importance of body tissue composition to calorimetric assessments of ice content in whole animals
inferredcites →https://doi.org/10.1038/282300a0openalex-snapshot
Thermal buffering in Afro-alpine plants due to nucleating agent-induced water freezing
inferredcites →https://doi.org/10.1098/rstb.1990.0035openalex-snapshot
Cold tolerance of insects and other arthropods
inferredcites →https://doi.org/10.1111/j.1463-6395.1981.tb00614.xopenalex-snapshot
Sense Organs of Two Marine Arthrotardigrades (Heterotardigrada, Tardigrada)
inferredcites →https://doi.org/10.1111/j.1469-185x.1989.tb00681.xopenalex-snapshot
ADAPTATIONS OF TERRESTRIAL ARTHROPODS TO THE ALPINE ENVIRONMENT
inferredcites →https://doi.org/10.1139/z90-074openalex-snapshot
Inoculation triggers freezing at high subzero temperatures in a freeze-tolerant frog (Rana sylvatica) and insect (Eurosta solidaginis)
inferredcites →https://doi.org/10.1146/annurev.ph.45.030183.001401openalex-snapshot
The Role of Hemolymph Proteins in the Cold Tolerance of Insects
inferredcites →https://doi.org/10.1152/physrev.1985.65.4.799openalex-snapshot
Physiology of cold tolerance in insects
inferredcites →https://doi.org/10.1152/physrev.1988.68.1.27openalex-snapshot
Freeze tolerance in animals
inferredcites →https://doi.org/10.2307/1311113openalex-snapshot
Insect Cold-Hardiness: To Freeze or Not to Freeze
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5852/ejt.2025.981.2823zenodo-depositor-declared
Taxonomic reanalysis of the genus Richtersius (Tardigrada; Eutardigrada), with description of two new species from Italy and Sweden
inferred← citeshttps://doi.org/10.1002/9781119593096.ch12openalex-snapshot
Tardigrades – Evolutionary Explorers in Extreme Environments
inferred← citeshttps://doi.org/10.1002/jez.10186openalex-snapshot
Experimentally induced anhydrobiosis in the tardigrade Richtersius coronifer: phenotypic factors affecting survival
inferred← citeshttps://doi.org/10.1007/978-3-030-21213-1_3openalex-snapshot
Dormancy in Freshwater Tardigrades
inferred← citeshttps://doi.org/10.1007/978-3-319-95702-9_11openalex-snapshot
Environmental Adaptations: Cryobiosis
inferred← citeshttps://doi.org/10.1007/978-3-319-95702-9_9openalex-snapshot
Environmental Adaptations: Encystment and Cyclomorphosis
inferred← citeshttps://doi.org/10.1007/978-3-662-06285-2_8openalex-snapshot
Cold adaptations in terrestrial invertebrates
inferred← citeshttps://doi.org/10.1007/bf00239062openalex-snapshot
Cold tolerance in Tardigrada from Dronning Maud Land, Antarctica
inferred← citeshttps://doi.org/10.1007/bf00346448openalex-snapshot
Dehydration of earthworm cocoons exposed to cold: a novel cold hardiness mechanism
inferred← citeshttps://doi.org/10.1007/bf00387308openalex-snapshot
Effects of dehydration on water relations and survival of lumbricid earthworm egg capsules
inferred← citeshttps://doi.org/10.1007/s00300-016-1931-0openalex-snapshot
Comparative analyses of Bertolanius species (Eohypsibiidae; Eutardigrada) with the description of Bertolanius birnae sp. nov. from northern polar regions
inferred← citeshttps://doi.org/10.1007/s00709-016-1027-2openalex-snapshot
The structure of the desiccated Richtersius coronifer (Richters, 1903)
inferred← citeshttps://doi.org/10.1007/s10152-014-0409-0openalex-snapshot
First record of cysts in the tidal tardigrade Echiniscoides sigismundi
inferred← citeshttps://doi.org/10.1007/s10750-005-1407-7openalex-snapshot
Encystment Processes and the “Matrioshka-like Stage” in a Moss-dwelling and in a Limnic Species of Eutardigrades (Tardigrada)
inferred← citeshttps://doi.org/10.1007/s10750-019-04144-6openalex-snapshot
Extreme-tolerance mechanisms in meiofaunal organisms: a case study with tardigrades, rotifers and nematodes
inferred← citeshttps://doi.org/10.1016/0300-9629(96)00010-2openalex-snapshot
Physiology of cold hardiness in earthworms
inferred← citeshttps://doi.org/10.1016/b978-0-12-374855-3.00027-3openalex-snapshot
Literature Citations
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11439-4openalex-snapshot
Aging of the Tardigrades
inferred← citeshttps://doi.org/10.1016/j.cbpa.2010.01.015openalex-snapshot
Ice crystallization and freeze tolerance in embryonic stages of the tardigrade Milnesium tardigradum
inferred← citeshttps://doi.org/10.1016/j.cbpa.2022.111245openalex-snapshot
Extreme freeze-tolerance in cryophilic tardigrades relies on controlled ice formation but does not involve significant change in transcription
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2011.03.003openalex-snapshot
On dormancy strategies in tardigrades
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2011.03.018openalex-snapshot
Dormant stages in freshwater bryozoans—An adaptation to transcend environmental constraints
inferred← citeshttps://doi.org/10.1016/j.zool.2010.11.005openalex-snapshot
Survival of freezing by hydrated tardigrades inhabiting terrestrial and freshwater habitats
inferred← citeshttps://doi.org/10.1046/j.1365-2427.2000.00586.xopenalex-snapshot
The biology and ecology of lotic Tardigrada
inferred← citeshttps://doi.org/10.1078/0044-5231-00062openalex-snapshot
Cryptobiosis in the Eutardigrade Adorybiotus (Richtersius) coronifer: Tolerance to Alcohols, Temperature and de novo Protein Synthesis
inferred← citeshttps://doi.org/10.1078/0044-5231-00068openalex-snapshot
Cryptobiosis 300 Years on from van Leuwenhoek: What Have We Learned about Tardigrades?
inferred← citeshttps://doi.org/10.1080/07924259.1994.9672407openalex-snapshot
Maturative pattern of ovary and testis in eutardigrades of freshwater and terrestrial habitats
inferred← citeshttps://doi.org/10.1093/czoolo/56.2.259openalex-snapshot
Comparative studies on storage cells in tardigrades during starvation and anhydrobiosis
inferred← citeshttps://doi.org/10.1093/icb/42.3.652openalex-snapshot
Current Status of the Tardigrada: Evolution and Ecology
inferred← citeshttps://doi.org/10.1111/j.1439-0469.2010.00605.xopenalex-snapshot
Extreme stress tolerance in tardigrades: surviving space conditions in low earth orbit
inferred← citeshttps://doi.org/10.1111/j.1469-185x.1995.tb01442.xopenalex-snapshot
COLD TOLERANCE STRATEGIES IN NEMATODES
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2003.tb00069.xopenalex-snapshot
Reproductive modes and genetic polymorphism in the tardigrade Richtersius coronifer (Eutardigrada, Macrobiotidae)
inferred← citeshttps://doi.org/10.1111/j.1748-1716.2011.02252.xopenalex-snapshot
Survival in extreme environments – on the current knowledge of adaptations in tardigrades
inferred← citeshttps://doi.org/10.1111/jzo.13018openalex-snapshot
Reduced ageing in the frozen state in the tardigrade Milnesium inceptum (Eutardigrada: Apochela)
inferred← citeshttps://doi.org/10.1163/18759866-07901002openalex-snapshot
Movement behaviour and video tracking of Milnesium tardigradum Doyère, 1840 (Eutardigrada, Apochela)
inferred← citeshttps://doi.org/10.1186/s40851-020-0154-yopenalex-snapshot
A new redescription of Richtersius coronifer, supported by transcriptome, provides resources for describing concealed species diversity within the monotypic genus Richtersius (Eutardigrada)
inferred← citeshttps://doi.org/10.1242/jeb.00935openalex-snapshot
Stress gene (hsp70) sequences and quantitative expression inMilnesium tardigradum(Tardigrada) during active and cryptobiotic stages
inferred← citeshttps://doi.org/10.1242/jeb.015131openalex-snapshot
Diapause in tardigrades: a study of factors involved in encystment
inferred← citeshttps://doi.org/10.1242/jeb.025973openalex-snapshot
Freeze tolerance, supercooling points and ice formation: comparative studies on the subzero temperature survival of limno-terrestrial tardigrades
inferred← citeshttps://doi.org/10.1242/jeb.029413openalex-snapshot
Cyclomorphosis in Tardigrada: adaptation to environmental constraints
inferred← citeshttps://doi.org/10.1242/jeb.075531openalex-snapshot
Inorganic ion composition in Tardigrada: cryptobionts contain large fraction of unidentified organic solutes
inferred← citeshttps://doi.org/10.14411/eje.2003.049openalex-snapshot
Activity and dormancy in relation to body water and cold tolerance in a winter-active springtail (Collembola)
inferred← citeshttps://doi.org/10.2307/1552128openalex-snapshot
Distribution, Community Structure, and Microhabitats of Soil Invertebrates along an Elevational Gradient in Taylor Valley, Antarctica
inferred← citeshttps://doi.org/10.3184/003685003783238680openalex-snapshot
Water or Ice? — the Challenge for Invertebrate Cold Survival
inferred← citeshttps://doi.org/10.3390/d12020062openalex-snapshot
Analysis of Encystment, Excystment, and Cyst Structure in Freshwater Eutardigrade Thulinius ruffoi (Tardigrada, Isohypsibioidea: Doryphoribiidae)
inferred← citeshttps://doi.org/10.4081/jlimnol.2004.s1.16openalex-snapshot
Experiences with dormancy in tardigrades
inferred← citeshttps://doi.org/10.4172/2332-2519.1000121openalex-snapshot
Tardigrade Exposure to Outer Space Conditions - An Experimental Validation
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