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Rapid cold hardening: ecological relevance, physiological mechanisms and new perspectives
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/qj.49708837708openalex-snapshot
Wind, temperature and humidity distribution at some cold fronts over SE. England
inferredcites →https://doi.org/10.1007/bf00258982openalex-snapshot
A comparison of the responses of tropical and temperate flies (Diptera: Sarcophagidae) to cold and heat stress
inferredcites →https://doi.org/10.1007/s00300-019-02503-6openalex-snapshot
Characterization of drought-induced rapid cold-hardening in the Antarctic midge, Belgica antarctica
inferredcites →https://doi.org/10.1007/s00360-007-0172-5openalex-snapshot
Shifts in the carbohydrate, polyol, and amino acid pools during rapid cold-hardening and diapause-associated cold-hardening in flesh flies (Sarcophaga crassipalpis): a metabolomic comparison
inferredcites →https://doi.org/10.1007/s00360-016-1030-0openalex-snapshot
Desiccation enhances rapid cold-hardening in the flesh fly Sarcophaga bullata: evidence for cross tolerance between rapid physiological responses
inferredcites →https://doi.org/10.1007/s10493-014-9803-1openalex-snapshot
Rapid cold hardening response in the predatory mite Neoseiulus californicus
inferredcites →https://doi.org/10.1007/s10495-006-0048-2openalex-snapshot
Rapid cold-hardening protects Drosophila melanogaster from cold-induced apoptosis
inferredcites →https://doi.org/10.1007/s10495-010-0570-0openalex-snapshot
Rapid cold-hardening blocks cold-induced apoptosis by inhibiting the activation of pro-caspases in the flesh fly Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1007/s10522-006-9075-1openalex-snapshot
Heat-induced hormesis in longevity of two sibling Drosophila species
inferredcites →https://doi.org/10.1007/s10522-013-9436-5openalex-snapshot
Low doses of radiation can enhance insect lifespans
inferredcites →https://doi.org/10.1007/s10522-013-9458-zopenalex-snapshot
Fasting can protect young and middle-aged Drosophila melanogaster flies against a severe cold stress
inferredcites →https://doi.org/10.1016/0022-1910(90)90176-gopenalex-snapshot
Acclimation for desiccation resistance in Drosophila melanogaster and the association between acclimation responses and genetic variation
inferredcites →https://doi.org/10.1016/0022-1910(91)90026-vopenalex-snapshot
Anoxia induces rapid cold hardening in the housefly Musca domestica (Diptera: Muscidae)
inferredcites →https://doi.org/10.1016/0022-1910(92)90118-wopenalex-snapshot
Effect of rapid cold hardening on reproduction and survival of offspring in the housefly Musca domestica
inferredcites →https://doi.org/10.1016/0022-1910(94)90019-1openalex-snapshot
Cold tolerance including rapid cold-hardening and inoculative freezing of fall migrant monarch butterflies in Ohio
inferredcites →https://doi.org/10.1016/0300-9629(87)90011-9openalex-snapshot
Time courses of thermal acclimation for critical thermal minima in the salamanders Desmognathus quadramaculatus, Desmognathus monticola, Desmognathus ochrophaeus, and Plethodon jordani
inferredcites →https://doi.org/10.1016/0967-0653(93)90022-yopenalex-snapshot
10.1016/0967-0653(93)90022-y
inferredcites →https://doi.org/10.1016/j.aspen.2018.09.010openalex-snapshot
Calcium/calmodulin-dependent protein kinase II of the oriental fruit fly, Bactrocera dorsalis, and its association with rapid cold hardiness
inferredcites →https://doi.org/10.1016/j.cbpa.2007.01.301openalex-snapshot
Rapid cold-hardening: Ecological significance and underlying mechanisms
inferredcites →https://doi.org/10.1016/j.cbpa.2017.06.019openalex-snapshot
Effects of nutrient and water restriction on thermal tolerance: A test of mechanisms and hypotheses
inferredcites →https://doi.org/10.1016/j.cbpa.2019.04.007openalex-snapshot
Rapid cold hardening and octopamine modulate chill tolerance in Locusta migratoria
inferredcites →https://doi.org/10.1016/j.cbpa.2020.110774openalex-snapshot
Effects of brief chilling and desiccation on ion homeostasis in the central nervous system of the migratory locust, Locusta migratoria
inferredcites →https://doi.org/10.1016/j.cryobiol.2006.03.003openalex-snapshot
Rapid cold-hardening increases membrane fluidity and cold tolerance of insect cells
inferredcites →https://doi.org/10.1016/j.cryobiol.2008.01.001openalex-snapshot
Rapid thermal adaptation during field temperature variations in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.gene.2017.11.002openalex-snapshot
Identification and analysis of up-regulated proteins in Lissorhoptrus oryzophilus adults for rapid cold hardening
inferredcites →https://doi.org/10.1016/j.jinsphys.2004.01.003openalex-snapshot
Cold shock injury and ecological costs of rapid cold hardening in the grain aphid Sitobion avenae (Hemiptera: Aphididae)
inferredcites →https://doi.org/10.1016/j.jinsphys.2005.06.007openalex-snapshot
Changes in membrane lipid composition following rapid cold hardening in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.jinsphys.2005.09.007openalex-snapshot
Complexity of the cold acclimation response in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.jinsphys.2005.10.005openalex-snapshot
Stress-induced accumulation of glycerol in the flesh fly, Sarcophaga bullata: Evidence indicating anti-desiccant and cryoprotectant functions of this polyol and a role for the brain in coordinating the response
inferredcites →https://doi.org/10.1016/j.jinsphys.2006.07.001openalex-snapshot
The effects of carbon dioxide anesthesia and anoxia on rapid cold-hardening and chill coma recovery in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.jinsphys.2006.07.005openalex-snapshot
Oleic acid is elevated in cell membranes during rapid cold-hardening and pupal diapause in the flesh fly, Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1016/j.jinsphys.2007.06.012openalex-snapshot
Metabolomic profiling of rapid cold hardening and cold shock in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.jinsphys.2007.08.007openalex-snapshot
Thermal tolerance in a south-east African population of the tsetse fly Glossina pallidipes (Diptera, Glossinidae): Implications for forecasting climate change impacts
inferredcites →https://doi.org/10.1016/j.jinsphys.2008.11.015openalex-snapshot
Membrane remodeling and glucose in Drosophila melanogaster: A test of rapid cold-hardening and chilling tolerance hypotheses
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.09.002openalex-snapshot
Rapid changes in desiccation resistance in Drosophila melanogaster are facilitated by changes in cuticular permeability
inferredcites →https://doi.org/10.1016/j.jinsphys.2012.05.009openalex-snapshot
Pre-adapted to the maritime Antarctic? – Rapid cold hardening of the midge, Eretmoptera murphyi
inferredcites →https://doi.org/10.1016/j.jinsphys.2012.09.006openalex-snapshot
Cold hardening modulates K+ homeostasis in the brain of Drosophila melanogaster during chill coma
inferredcites →https://doi.org/10.1016/j.jinsphys.2013.07.008openalex-snapshot
Feeding impairs chill coma recovery in the migratory locust (Locusta migratoria)
inferredcites →https://doi.org/10.1016/j.jinsphys.2014.01.009openalex-snapshot
The rapid cold hardening response of Drosophila melanogaster: Complex regulation across different levels of biological organization
inferredcites →https://doi.org/10.1016/j.jinsphys.2014.06.010openalex-snapshot
A specific glycerol kinase induces rapid cold hardening of the diamondback moth, Plutella xylostella
inferredcites →https://doi.org/10.1016/j.jinsphys.2014.12.004openalex-snapshot
The limits of drought-induced rapid cold-hardening: Extremely brief, mild desiccation triggers enhanced freeze-tolerance in Eurosta solidaginis larvae
inferredcites →https://doi.org/10.1016/j.jinsphys.2016.10.009openalex-snapshot
Does cold activate the Drosophila melanogaster immune system?
inferredcites →https://doi.org/10.1016/j.jtherbio.2004.09.001openalex-snapshot
Acclimation, heat shock and hardening
inferredcites →https://doi.org/10.1016/j.jtherbio.2004.12.005openalex-snapshot
Acclimation, heat shock and hardening—a response from evolutionary biology
inferredcites →https://doi.org/10.1016/j.jtherbio.2009.05.002openalex-snapshot
Low-temperature tolerance of false codling moth Thaumatotibia leucotreta (Meyrick) (Lepidoptera: Tortricidae) in South Africa
inferredcites →https://doi.org/10.1016/j.jtherbio.2016.03.005openalex-snapshot
Identification, genomic organization and expression profiles of four heat shock protein genes in the western flower thrips, Frankliniella occidentalis
inferredcites →https://doi.org/10.1016/j.jtherbio.2017.03.012openalex-snapshot
Low temperature tolerance, cold hardening and acclimation in tadpoles of the neotropical túngara frog ( Engystomops pustulosus )
inferredcites →https://doi.org/10.1016/j.jtherbio.2018.06.011openalex-snapshot
Speed of exposure to rapid cold hardening and genotype drive the level of acclimation response in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.scitotenv.2009.10.067openalex-snapshot
Interactions between effects of environmental chemicals and natural stressors: A review
inferredcites →https://doi.org/10.1016/s0014-5793(99)00660-2openalex-snapshot
A RNA polymerase with transcriptional activity at 0°C from the Antarctic bacterium Pseudomonas syringae
inferredcites →https://doi.org/10.1016/s0022-1910(00)00141-4openalex-snapshot
Cold tolerance and proline metabolic gene expression in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/s0022-1910(00)00162-1openalex-snapshot
Rapid cold hardening in the predatory mite Euseius (Amblyseius) finlandicus (Acari: Phytoseiidae)
inferredcites →https://doi.org/10.1016/s0022-1910(02)00225-1openalex-snapshot
Rapid responses to high temperature and desiccation but not to low temperature in the freeze tolerant sub-Antarctic caterpillar Pringleophaga marioni (Lepidoptera, Tineidae)
inferredcites →https://doi.org/10.1016/s0022-1910(99)00040-2openalex-snapshot
Induction of rapid cold hardening by cooling at ecologically relevant rates in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/s0022-474x(98)00031-9openalex-snapshot
Rapid cold hardening capacity in five species of coleopteran pests of stored grain
inferredcites →https://doi.org/10.1016/s1226-8615(08)60256-3openalex-snapshot
Spatial Conditioning in the Flesh Fly, Sarcophaga crassipal pis: Disruption of Learning by Cold Shock and Protection by Rapid Cold Hardening
inferredcites →https://doi.org/10.1016/s2095-3119(12)60014-8openalex-snapshot
p38 MAPK is a Component of the Signal Transduction Pathway Triggering Cold Stress Response in the MED Cryptic Species of Bemisia tabaci
inferredcites →https://doi.org/10.1017/cbo9780511675997.002openalex-snapshot
A primer on insect cold-tolerance
inferredcites →https://doi.org/10.1017/cbo9780511675997.003openalex-snapshot
Rapid cold-hardening: Ecological significance and underpinning mechanisms
inferredcites →https://doi.org/10.1017/cbo9780511675997.006openalex-snapshot
Cell structural modifications in insects at low temperatures
inferredcites →https://doi.org/10.1021/acs.jproteome.6b00427openalex-snapshot
Quantitative Phosphoproteomics Reveals Signaling Mechanisms Associated with Rapid Cold Hardening in a Chill-Tolerant Fly
inferredcites →https://doi.org/10.1021/bk-2017-1249.ch008openalex-snapshot
Occurrence and Significance of Insecticide-Induced Hormesis in Insects
inferredcites →https://doi.org/10.1038/nclimate2378openalex-snapshot
Recent geographic convergence in diurnal and annual temperature cycling flattens global thermal profiles
inferredcites →https://doi.org/10.1038/srep28999openalex-snapshot
Cold acclimation wholly reorganizes the Drosophila melanogaster transcriptome and metabolome
inferredcites →https://doi.org/10.1046/j.1365-3032.2000.00201.xopenalex-snapshot
Thermotolerance and rapid cold hardening ameliorate the negative effects of brief exposures to high or low temperatures on fecundity in the flesh fly, Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1046/j.1570-7458.2001.00910.xopenalex-snapshot
Rapid cold hardening in the olive fruit fly Bactrocera oleae under laboratory and field conditions
inferredcites →https://doi.org/10.1073/pnas.1306705110openalex-snapshot
Calcium signaling mediates cold sensing in insect tissues
inferredcites →https://doi.org/10.1073/pnas.1503456112openalex-snapshot
Constraints, independence, and evolution of thermal plasticity: Probing genetic architecture of long- and short-term thermal acclimation
inferredcites →https://doi.org/10.1073/pnas.1813532115openalex-snapshot
Cold exposure causes cell death by depolarization-mediated Ca 2+ overload in a chill-susceptible insect
inferredcites →https://doi.org/10.1073/pnas.71.2.522openalex-snapshot
Homeoviscous Adaptation—A Homeostatic Process that Regulates the Viscosity of Membrane Lipids in Escherichia coli
inferredcites →https://doi.org/10.1086/605416openalex-snapshot
Brief Chilling to Subzero Temperature Increases Cold Hardiness in the Hatchling Painted Turtle (Chrysemys picta)
inferredcites →https://doi.org/10.1086/physzool.60.3.30162282openalex-snapshot
Cold-Shock Injury and Rapid Cold Hardening in the Flesh Fly Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1093/ee/nvx153openalex-snapshot
Rapid Cold-Hardening of a Subtropical Species, Maruca vitrata (Lepidoptera: Crambidae), Accompanies Hypertrehalosemia by Upregulating Trehalose-6-Phosphate Synthase
inferredcites →https://doi.org/10.1093/icb/ict004openalex-snapshot
Cross-tolerance and Cross-talk in the Cold: Relating Low Temperatures to Desiccation and Immune Stress in Insects
inferredcites →https://doi.org/10.1093/icb/icw024openalex-snapshot
Life in the Frequency Domain: the Biological Impacts of Changes in Climate Variability at Multiple Time Scales
inferredcites →https://doi.org/10.1098/rspb.2009.1807openalex-snapshot
Repeated stress exposure results in a survival–reproduction trade-off inDrosophila melanogaster
inferredcites →https://doi.org/10.1101/2020.01.01.887414openalex-snapshot
Brief exposure to a diverse range of environmental stress enhances stress tolerance in the polyextremophilic Antarctic midge, Belgica antarctica
inferredcites →https://doi.org/10.1101/gad.12.24.3788openalex-snapshot
Regulation of the heat shock transcriptional response: cross talk between a family of heat shock factors, molecular chaperones, and negative regulators
inferredcites →https://doi.org/10.1111/1365-2435.12255openalex-snapshot
Rapid acclimation to cold allows the cane toad to invade montane areas within its Australian range
inferredcites →https://doi.org/10.1111/j.1365-2435.2005.01025.xopenalex-snapshot
Hardening capacity in the Drosophila melanogaster species group is constrained by basal thermotolerance
inferredcites →https://doi.org/10.1111/j.1365-2435.2008.01503.xopenalex-snapshot
The rapid cold hardening response of Collembola is influenced by thermal variability of the habitat
inferredcites →https://doi.org/10.1111/j.1365-2435.2011.01898.xopenalex-snapshot
Comparing phenotypic effects and molecular correlates of developmental, gradual and rapid cold acclimation responses in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-2583.2005.00589.xopenalex-snapshot
Cold hardening and transcriptional change in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00739.xopenalex-snapshot
Gene transcription during exposure to, and recovery from, cold and desiccation stress in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-2583.2008.00827.xopenalex-snapshot
Rapid cold hardening elicits changes in brain protein profiles of the flesh fly, Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1111/j.1365-2583.2011.01119.xopenalex-snapshot
Cold tolerance and cold‐induced modulation of gene expression in two Drosophila virilis group species with different distributions
inferredcites →https://doi.org/10.1111/j.1365-2915.1996.tb00743.xopenalex-snapshot
Adaptive larval thermotolerance and induced cross‐tolerance to propoxur insecticide in mosquitoes Anopheles stephensi and Aedes aegypti
inferredcites →https://doi.org/10.1111/j.1365-3032.1991.tb00539.xopenalex-snapshot
Cold shock and heat shock: a comparison of the protection generated by brief pretreatment at less severe temperatures
inferredcites →https://doi.org/10.1111/j.1365-3032.1996.tb00866.xopenalex-snapshot
Cold shock and rapid cold‐hardening of pharate adult flesh flies (Sarcophaga crassipalpis): effects on behaviour and neuromuscular function following eclosion
inferredcites →https://doi.org/10.1111/j.1365-3032.2006.00522.xopenalex-snapshot
Reorganization of membrane lipids during fast and slow cold hardening in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-3032.2007.00584.xopenalex-snapshot
Rapid cold‐hardening of Drosophila melanogaster in a field setting
inferredcites →https://doi.org/10.1111/j.1420-9101.2011.02324.xopenalex-snapshot
Basal cold but not heat tolerance constrains plasticity among Drosophila species (Diptera: Drosophilidae)
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01419.xopenalex-snapshot
FITNESS COSTS OF RAPID COLD-HARDENING IN CERATITIS CAPITATA
inferredcites →https://doi.org/10.1111/jeb.13244openalex-snapshot
Genetic variation in the shape of cold‐survival curves in a single fly population suggests potential for selection from climate variability
inferredcites →https://doi.org/10.1111/phen.12019openalex-snapshot
Physiological mechanisms of seasonal and rapid cold‐hardening in insects
inferredcites →https://doi.org/10.1111/phen.12191openalex-snapshot
The persistence of short‐term cold acclimation in D rosophila melanogaster ( D iptera: D rosophilidae)
inferredcites →https://doi.org/10.1126/science.1083073openalex-snapshot
Acclimation Capacity Underlies Susceptibility to Climate Change
inferredcites →https://doi.org/10.1126/science.238.4832.1415openalex-snapshot
A Rapid Cold-Hardening Process in Insects
inferredcites →https://doi.org/10.1139/cjz-2014-0147openalex-snapshot
Stress tolerance in a polyextremophile: the southernmost insect
inferredcites →https://doi.org/10.1146/annurev-ento-010715-023859openalex-snapshot
What Can Plasticity Contribute to Insect Responses to Climate Change?
inferredcites →https://doi.org/10.1146/annurev-genet-102808-114910openalex-snapshot
Regulation Mechanisms and Signaling Pathways of Autophagy
inferredcites →https://doi.org/10.1146/annurev-physiol-022516-034142openalex-snapshot
The Integrative Physiology of Insect Chill Tolerance
inferredcites →https://doi.org/10.1146/annurev.en.06.010161.000415openalex-snapshot
Principles of Insect Cold-Hardiness
inferredcites →https://doi.org/10.1152/ajpregu.00459.2007openalex-snapshot
Rapid cold-hardening in larvae of the Antarctic midgeBelgica antarctica:cellular cold-sensing and a role for calcium
inferredcites →https://doi.org/10.1152/ajpregu.1988.255.4.r628openalex-snapshot
Time course of thermal adaptation in plasma membranes of trout kidney. II. Molecular species composition
inferredcites →https://doi.org/10.1152/physiolgenomics.00042.2012openalex-snapshot
Combined transcriptomic and metabolomic approach uncovers molecular mechanisms of cold tolerance in a temperate flesh fly
inferredcites →https://doi.org/10.1242/jeb.006536openalex-snapshot
p38 MAPK is a likely component of the signal transduction pathway triggering rapid cold hardening in the flesh fly Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1242/jeb.00951openalex-snapshot
Preservation of reproductive behaviors during modest cooling: rapid cold-hardening fine-tunes organismal response
inferredcites →https://doi.org/10.1242/jeb.01685openalex-snapshot
Low temperature acclimated populations of the grain aphidSitobion avenaeretain ability to rapidly cold harden with enhanced fitness
inferredcites →https://doi.org/10.1242/jeb.02001openalex-snapshot
Rapid cold-hardening increases the freezing tolerance of the Antarctic midge Belgica antarctica
inferredcites →https://doi.org/10.1242/jeb.051912openalex-snapshot
Survival and energetic costs of repeated cold exposure in the Antarctic midge, Belgica antarctica : a comparison between frozen and supercooled larvae
inferredcites →https://doi.org/10.1242/jeb.059956openalex-snapshot
The impacts of repeated cold exposure on insects
inferredcites →https://doi.org/10.1242/jeb.060624openalex-snapshot
Survival and energetic costs of repeated cold exposure in the Antarctic midge, Belgica antarctica: a comparison between frozen and supercooled larvae
inferredcites →https://doi.org/10.1242/jeb.065631openalex-snapshot
Short-term anoxic conditioning hormesis boosts antioxidant defenses, lowers oxidative damage following irradiation and enhances male sexual performance in the Caribbean fruit fly, Anastrepha suspensa
inferredcites →https://doi.org/10.1242/jeb.069658openalex-snapshot
Changes in extreme cold tolerance, membrane composition and cardiac transcriptome during the first day of thermal acclimation in the porcelain crabPetrolisthes cinctipes
inferredcites →https://doi.org/10.1242/jeb.076885openalex-snapshot
Mild desiccation rapidly increases freeze tolerance of the goldenrod gall fly, Eurosta solidaginis: evidence for drought-induced RCH
inferredcites →https://doi.org/10.1242/jeb.081141openalex-snapshot
Rapid cold hardening improves recovery of ion homeostasis and chill coma recovery in the migratory locustLocusta migratoria
inferredcites →https://doi.org/10.1242/jeb.088278openalex-snapshot
The protective effect of rapid cold-hardening develops more quickly in frozen versus supercooled larvae of the Antarctic midge, Belgica antarctica
inferredcites →https://doi.org/10.1242/jeb.092031openalex-snapshot
RNA interference of glycerol biosynthesis suppresses rapid cold hardening of the beet armyworm,Spodoptera exigua
inferredcites →https://doi.org/10.1242/jeb.148.1.245openalex-snapshot
A rapid cold-hardening response protecting against cold shock injury in Drosophila melanogaster
inferredcites →https://doi.org/10.1242/jeb.204.9.1659openalex-snapshot
Rapid Cold-Hardening of Drosophila Melanogaster (Diptera: Drosophilidae) During Ecologically Based Thermoperiodic Cycles
inferredcites →https://doi.org/10.1242/jeb.206011openalex-snapshot
Rapid cold hardening protects against sublethal freezing injury in an Antarctic insect
inferredcites →https://doi.org/10.1371/journal.pbio.1000357openalex-snapshot
Adaptation, Plasticity, and Extinction in a Changing Environment: Towards a Predictive Theory
inferredcites →https://doi.org/10.1371/journal.pone.0080061openalex-snapshot
Can Winter-Active Bumblebees Survive the Cold? Assessing the Cold Tolerance of Bombus terrestris audax and the Effects of Pollen Feeding
inferredcites →https://doi.org/10.1371/journal.pone.0197822openalex-snapshot
Costs of cold acclimation on survival and reproductive behavior in Drosophila melanogaster
inferredcites →https://doi.org/10.1603/ec13370openalex-snapshot
Low-Oxygen Atmospheric Treatment Improves the Performance of Irradiation-Sterilized Male Cactus Moths Used in SIT
inferredcites →https://doi.org/10.1674/0003-0031(1998)140[0027:soiaab]2.0.co;2openalex-snapshot
Survival of Immersion and Anoxia by Larval Tiger Beetles, Cicindela togata
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4768883openalex-extracted
The Role of Life Stage and Season in Carrion Beetle Thermal Tolerance
inferred← citeshttps://doi.org/10.1002/arch.70208openalex-snapshot
Comparison of Thermal Tolerance Between Spodoptera frugiperda and Spodoptera litura (Lepidoptera: Noctuidae)
inferred← citeshttps://doi.org/10.1007/5584_2024_805openalex-snapshot
Insect Lipids: Structure, Classification, and Function
inferred← citeshttps://doi.org/10.1007/978-3-032-04842-4_805openalex-snapshot
Insect Lipids: Structure, Classification and Function
inferred← citeshttps://doi.org/10.1007/s10493-022-00771-2openalex-snapshot
Rapid cold hardening response of the phytoseiid mite Neoseiulus striatus: increased cold tolerance but not reduced predation
inferred← citeshttps://doi.org/10.1007/s10493-025-01100-zopenalex-snapshot
Cold tolerance of Panonychus citri (McGregor) (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.1007/s10682-021-10116-xopenalex-snapshot
Plasticity in thermal hardening of the invasive Asian house gecko
inferred← citeshttps://doi.org/10.1016/j.afres.2026.101860openalex-snapshot
Dehydration-induced changes in physical and volatile characteristics of house cricket (Acheta domesticus) powder
inferred← citeshttps://doi.org/10.1016/j.aspen.2021.101862openalex-snapshot
Effect of cold acclimation and rapid cold-hardening on the survival of Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae) under cold stress
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2024.105651openalex-snapshot
Intraspecific variation in rapid cold hardening and acclimation of the adventive parrot’s feather weevil, Phytobius (=Parenthis) vestitus, in the southern USA
inferred← citeshttps://doi.org/10.1016/j.cbpa.2021.110966openalex-snapshot
Cold hardening improves larval tick questing under low temperatures at the expense of longevity
inferred← citeshttps://doi.org/10.1016/j.cbpa.2021.110998openalex-snapshot
Plasticity of cold hardiness in the eastern spruce budworm, Choristoneura fumiferana
inferred← citeshttps://doi.org/10.1016/j.cbpa.2021.111037openalex-snapshot
Editorial on combatting the cold: Comparative physiology of low temperature and related stressors in arthropods
inferred← citeshttps://doi.org/10.1016/j.cbpa.2023.111511openalex-snapshot
Rapid cold hardening modifies ion regulation to delay anoxia-induced spreading depolarization in the CNS of the locust
inferred← citeshttps://doi.org/10.1016/j.cois.2023.101055openalex-snapshot
A cold and quiet brain: mechanisms of insect CNS arrest at low temperatures
inferred← citeshttps://doi.org/10.1016/j.conb.2024.102885openalex-snapshot
Resilience of circuits to environmental challenge
inferred← citeshttps://doi.org/10.1016/j.cub.2024.03.019openalex-snapshot
The tardigrade Hypsibius exemplaris dramatically upregulates DNA repair pathway genes in response to ionizing radiation
inferred← citeshttps://doi.org/10.1016/j.envpol.2026.128721openalex-snapshot
Pollution constrains thermal adaptation but not thermoregulation in dung beetles
inferred← citeshttps://doi.org/10.1016/j.ibmb.2025.104426openalex-snapshot
Genome-wide analysis of the spider Pardosa pseudoannulata revealed the function of spliceosome components in cold adaptation
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.136861openalex-snapshot
Functional and evolutionary analysis of key enzymes triacylglycerol lipase, glycogen hydrolases in the glycerol and glucose biosynthesis pathway and cellular chaperones for freeze-tolerance of the Rice stem borer, Chilo suppressalis
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.145838openalex-snapshot
Insights into the heat shock protein 19.9 and 90 in Bombyx mori: Key molecular chaperones in heat stress adaptation
inferred← citeshttps://doi.org/10.1016/j.isci.2021.102657openalex-snapshot
Identification of a neural basis for cold acclimation in Drosophila larvae
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2022.104360openalex-snapshot
Rapid cold hardening delays the onset of anoxia-induced coma via an octopaminergic pathway in Locusta migratoria
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2025.104844openalex-snapshot
Sex-dependent latent chilling injury changes estimates of thermal tolerance in a model insect
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2022.103395openalex-snapshot
Thermal tolerance responses of the two-spotted stink bug, Bathycoelia distincta (Hemiptera: Pentatomidae), vary with life stage and the sex of adults
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2025.104063openalex-snapshot
The role of life stage and season in critical thermal limits of carrion beetles
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2026.104526openalex-snapshot
Maternal and developmental temperature modulate adult response to temperature in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2026.104580openalex-snapshot
Rapid cold hardening improves tissue viability and facilitates recovery of activity following nonlethal cold exposure in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1017/s0007485326101102openalex-snapshot
The low-temperature tolerance of Cinara cedri (Hemiptera: Aphidoidea: Lachninae)
inferred← citeshttps://doi.org/10.1038/s41598-024-75146-1openalex-snapshot
Integrated transcriptional and biochemical profiling suggests mechanisms associated with rapid cold hardening in adult Liriomyza trifolii (Burgess)
inferred← citeshttps://doi.org/10.1038/s41598-025-95657-9openalex-snapshot
Cold hardiness of Corythucha marmorata (Hemiptera: Tingidae) on the functional crop Helianthus tuberosus
inferred← citeshttps://doi.org/10.1080/09583157.2025.2460036openalex-snapshot
Natural diets and cold acclimation, but not supplementary cryoprotectants, affect the cold tolerance of Hippodamia variegata
inferred← citeshttps://doi.org/10.1093/biolinnean/blad093openalex-snapshot
Environmental stress responses and adaptive evolution in the alpine ground beetle Nebria vandykei
inferred← citeshttps://doi.org/10.1093/ee/nvaf013openalex-snapshot
The lifelong effects of anoxia hormesis in solitary bees
inferred← citeshttps://doi.org/10.1093/ee/nvaf047openalex-snapshot
Time, temperature, and population affect the seasonal cold-hardening response of the adult stage of the mountain pine beetle (Coleoptera: Curculionidae)
inferred← citeshttps://doi.org/10.1093/evolut/qpaf151openalex-snapshot
Assessing the effect of experimental evolution under combined thermal-nutritional stress on larval thermotolerance and thermal plasticity in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1098/rspb.2022.2225openalex-snapshot
Effects of thermal fluctuations on biological processes: a meta-analysis of experiments manipulating thermal variability
inferred← citeshttps://doi.org/10.1101/2023.04.27.538621openalex-snapshot
Rapid cold hardening modifies mechanisms of ion regulation to delay anoxia-induced spreading depolarization in the CNS of Locusta migratoria
inferred← citeshttps://doi.org/10.1101/2023.09.07.556677openalex-snapshot
Tardigrades Dramatically Upregulate DNA Repair Pathway Genes in Response to Ionizing Radiation
inferred← citeshttps://doi.org/10.1101/2024.10.16.618698openalex-snapshot
Plasticity in cryoprotectant synthesis involves coordinated shunting away from pyruvate production
inferred← citeshttps://doi.org/10.1101/2025.05.12.653569openalex-snapshot
A hormetic model of rapid cold hardening in Drosophila melanogaster reveals threshold effects on survival and low fertility resilience
inferred← citeshttps://doi.org/10.1101/2025.05.30.656957openalex-snapshot
Heat-off responses of epidermal cells sensitize Drosophila larvae to noxious inputs
inferred← citeshttps://doi.org/10.1111/eea.70198openalex-snapshot
Time‐Course of Attainment and Reversal of Thermal Acclimation in the Invasive Fall Armyworm
inferred← citeshttps://doi.org/10.1111/eva.13120openalex-snapshot
Comparative transcriptomics of ice‐crawlers demonstrates cold specialization constrains niche evolution in a relict lineage
inferred← citeshttps://doi.org/10.1111/evo.14025openalex-snapshot
Distinct cold tolerance traits independently vary across genotypes inDrosophila melanogaster
inferred← citeshttps://doi.org/10.1111/mve.12709openalex-snapshot
Interindividual variation among Culex pipiens larvae in terms of thermal response
inferred← citeshttps://doi.org/10.1111/phen.12485openalex-snapshot
The physiological changes and the impact of rapid cold hardening on the survival ability of Dastarcus helophoroides (Fairmaire) (Coleoptera: Bothrideridae) under cold stress
inferred← citeshttps://doi.org/10.1111/phen.70058openalex-snapshot
Cold tolerance of adult African fig flies, Zaprionus indianus (Diptera: Drosophilidae)
inferred← citeshttps://doi.org/10.1146/annurev-ento-120120-095233openalex-snapshot
Molecular Mechanisms of Winter Survival
inferred← citeshttps://doi.org/10.1242/jeb.191262openalex-snapshot
Help, there are ‘omics’ in my comparative physiology!
inferred← citeshttps://doi.org/10.1242/jeb.236497openalex-snapshot
Metabolomic and transcriptomic responses of ticks during recovery from cold shock reveal mechanisms of survival
inferred← citeshttps://doi.org/10.1242/jeb.242506openalex-snapshot
Rapid stress hardening in the Antarctic midge improves male fertility by increasing courtship success and preventing decline of accessory gland proteins following cold exposure
inferred← citeshttps://doi.org/10.1242/jeb.244097openalex-snapshot
Rapid cold hardening increases axonal Na+/K+-ATPase activity and enhances performance of a visual motion detection circuit in Locusta migratoria
inferred← citeshttps://doi.org/10.1242/jeb.247040openalex-snapshot
A rapid return to normal: temporal gene expression patterns following cold exposure in the bumble bee Bombus impatiens
inferred← citeshttps://doi.org/10.1242/jeb.249675openalex-snapshot
Gain of thermal tolerance through acclimation is quicker than the loss by de-acclimation in the freeze-tolerant potworm, Enchytraeus albidus
inferred← citeshttps://doi.org/10.1242/jeb.250856openalex-snapshot
When is RCH not RCH? Rapid cold hardening has steep temperature thresholds inducing high survival but low fertility resilience to cold stress
inferred← citeshttps://doi.org/10.1371/journal.pone.0279254openalex-snapshot
Comparative transcriptome analysis of Liriomyza trifolii (Burgess) and Liriomyza sativae (Blanchard) (Diptera: Agromyzidae) in response to rapid cold hardening
inferred← citeshttps://doi.org/10.2139/ssrn.6174852openalex-snapshot
Effect of horizontal transfer of cold-tolerant substances of Ambrosia artemisiifolia on the low temperature adaptability of Ophraella communa
inferred← citeshttps://doi.org/10.2139/ssrn.7478105openalex-snapshot
Pancreatic lipase-related protein EoPLRP2 contributes to cold hardiness in the tea leafhopper Empoasca onukii
inferred← citeshttps://doi.org/10.3389/finsc.2024.1448766openalex-snapshot
RNA modifications in insects
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1544427openalex-snapshot
Alarming implications: severe fever with thrombocytopenia syndrome and its biological vectors in the context of climate change
inferred← citeshttps://doi.org/10.3389/fncel.2022.831803openalex-snapshot
Transient and Steady-State Properties of Drosophila Sensory Neurons Coding Noxious Cold Temperature
inferred← citeshttps://doi.org/10.3390/agronomy15030561openalex-snapshot
Transcriptomic Responses to Rapid Cold Hardening in Tomato Leafminer Adults: Implications for Tomato Leafminer Management
inferred← citeshttps://doi.org/10.3390/ani12040531openalex-snapshot
Temperature and Diet Acclimation Modify the Acute Thermal Performance of the Largest Extant Amphibian
inferred← citeshttps://doi.org/10.3390/biomedicines9030293openalex-snapshot
Less Can Be More: The Hormesis Theory of Stress Adaptation in the Global Biosphere and Its Implications
inferred← citeshttps://doi.org/10.3390/d15010047openalex-snapshot
How Might Climate Change Affect Adaptive Responses of Polar Arthropods?
inferred← citeshttps://doi.org/10.3390/insects12060549openalex-snapshot
Climate Mismatch between Introduced Biological Control Agents and Their Invasive Host Plants: Improving Biological Control of Tropical Weeds in Temperate Regions
inferred← citeshttps://doi.org/10.3390/insects12111041openalex-snapshot
Differential Response of Leafminer Flies Liriomyza trifolii (Burgess) and Liriomyza sativae (Blanchard) to Rapid Cold Hardening
inferred← citeshttps://doi.org/10.3390/insects14120903openalex-snapshot
Trehalose-6-Phosphate Synthase Contributes to Rapid Cold Hardening in the Invasive Insect Lissorhoptrus oryzophilus (Coleoptera: Curculionidae) by Regulating Trehalose Metabolism
inferred← citeshttps://doi.org/10.3390/insects15020090openalex-snapshot
Heat Shock Protein Genes Affect the Rapid Cold Hardening Ability of Two Invasive Tephritids
inferred← citeshttps://doi.org/10.3390/insects16090957openalex-snapshot
Thermal Adaptation in Liriomyza trifolii (Diptera: Agromyzidae): From Interspecific Competition to Mechanisms
inferred← citeshttps://doi.org/10.3390/insects17050488openalex-snapshot
Effect of Horizontal Transfer of Cold-Tolerant Substances of Ambrosia artemisiifolia on the Low Temperature Adaptability of Ophraella communa
inferred← citeshttps://doi.org/10.6620/zs.2020.59-25openalex-snapshot
Simultaneous Occurrence of Diapause and Cold Hardiness in Overwintering Eggs of the Apple Oystershell Scale, Lepidosaphes Malicola Borchsenius (Hem.: Diaspididae).
inferred← citeshttps://doi.org/10.70675/a2276397z5f66z4f66z92e2z72887129c4cdopenalex-snapshot
Conséquences phénotypiques et écophysiologiques des variations thermiques à court et long terme sur l'écologie saisonnière de la drosophile à ailes tachetées
inferred← citeshttps://doi.org/10.7717/peerj.12563openalex-snapshot
The metabolism and role of free fatty acids in key physiological processes in insects of medical, veterinary and forensic importance
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