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Physiological mechanisms of seasonal and rapid cold‐hardening in insects
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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.1402720402openalex-snapshot
Cryoprotective effects of thermal hysteresis protein on survivorship of frozen gut cells from the freeze‐tolerant centipede Lithobius forficatus
inferredcites →https://doi.org/10.1007/978-1-4757-0190-6_4openalex-snapshot
Biochemistry of Cryoprotectants
inferredcites →https://doi.org/10.1007/978-1-4757-0190-6_8openalex-snapshot
Relationship between Cold Hardiness and Diapause
inferredcites →https://doi.org/10.1007/bf00802756openalex-snapshot
Intermediary metabolism during low temperature acclimation in the overwintering gall fly larva,Eurosta solidaginis
inferredcites →https://doi.org/10.1007/s00360-004-0450-4openalex-snapshot
In vivo and in vitro rapid cold-hardening protects cells from cold-shock injury in the flesh fly
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/s00360-011-0552-8openalex-snapshot
A thermal hysteresis-producing xylomannan glycolipid antifreeze associated with cold tolerance is found in diverse taxa
inferredcites →https://doi.org/10.1007/s003600050165openalex-snapshot
Changes in fatty acid composition of phospholipids and triacylglycerols after cold-acclimation of an aestivating insect prepupa
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/10.1016/0022-1910(79)90083-0openalex-snapshot
Thermal-hysteresis-factors in overwintering insects
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/b0-44-451924-6/00043-0openalex-snapshot
Hormonal Control of Diapause
inferredcites →https://doi.org/10.1016/b978-0-12-384749-2.10010-xopenalex-snapshot
Hormonal Control of Diapause
inferredcites →https://doi.org/10.1016/j.bbabio.2009.01.005openalex-snapshot
Regulation of mitochondrial dehydrogenases by calcium ions
inferredcites →https://doi.org/10.1016/j.cbpb.2005.11.005openalex-snapshot
Chilling-injury and disturbance of ion homeostasis in the coxal muscle of the tropical cockroach (Nauphoeta cinerea)
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.2010.03.002openalex-snapshot
High temperature pulses decrease indirect chilling injury and elevate ATP levels in the flesh fly, Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1016/j.ibmb.2007.07.007openalex-snapshot
Upregulation of a desaturase is associated with the enhancement of cold hardiness in the onion maggot, Delia antiqua
inferredcites →https://doi.org/10.1016/j.jinsphys.2004.11.012openalex-snapshot
Gene expression of heat-shock proteins (Hsp23, Hsp70 and Hsp90) during and after larval diapause in the blow fly Lucilia sericata
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.2006.07.005openalex-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.2006.09.007openalex-snapshot
Upregulation of two actin genes and redistribution of actin during diapause and cold stress in the northern house mosquito, Culex pipiens
inferredcites →https://doi.org/10.1016/j.jinsphys.2007.01.003openalex-snapshot
Proteomics of the flesh fly brain reveals an abundance of upregulated heat shock proteins during pupal diapause
inferredcites →https://doi.org/10.1016/j.jinsphys.2007.05.012openalex-snapshot
Relationship between rapid cold-hardening and cold acclimation in the eggs of the yellow-spotted longicorn beetle, Psacothea hilaris
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.2007.12.011openalex-snapshot
Effects of acclimation temperature on thermal tolerance and membrane phospholipid composition in the fruit fly Drosophila melanogaster
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.2009.12.003openalex-snapshot
Changes in abundance of aquaporin-like proteins occurs concomitantly with seasonal acquisition of freeze tolerance in the goldenrod gall fly, Eurosta solidaginis
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.03.023openalex-snapshot
Expression of heat shock protein 70a mRNA in Bombyx mori diapause eggs
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.10.004openalex-snapshot
Mechanisms underlying insect chill-coma
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.01.012openalex-snapshot
Catalase and superoxide dismutase-2 enhance survival and protect ovaries during overwintering diapause in the mosquito Culex pipiens
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/s0021-9258(18)48354-8openalex-snapshot
Human HSP27 is phosphorylated at serines 78 and 82 by heat shock and mitogen-activated kinases that recognize the same amino acid motif as S6 kinase II.
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(01)00095-6openalex-snapshot
Differential expression of two HSP70 transcripts in response to cold shock, thermoperiod, and adult diapause in the Colorado potato beetle
inferredcites →https://doi.org/10.1016/s0022-1910(99)00221-8openalex-snapshot
Expression of Drosophila homologue of senescence marker protein-30 during cold acclimation
inferredcites →https://doi.org/10.1016/s0065-2806(03)31004-5openalex-snapshot
Trehalose – The Insect ‘Blood’ Sugar
inferredcites →https://doi.org/10.1016/s0169-5347(03)00014-4openalex-snapshot
Insects at low temperatures: an ecological perspective
inferredcites →https://doi.org/10.1016/s0965-1748(00)00021-7openalex-snapshot
Developmental upregulation of inducible hsp70 transcripts, but not the cognate form, during pupal diapause in the flesh fly, Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1016/s0965-1748(98)00046-0openalex-snapshot
Upregulation of a 23kDa small heat shock protein transcript during pupal diapause in the flesh fly, Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1016/s1096-4959(03)00117-9openalex-snapshot
Remodelling of membrane phospholipids during transition to diapause and cold-acclimation in the larvae of Chymomyza costata (Drosophilidae)
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/cbo9780511675997.004openalex-snapshot
Antifreeze and ice-nucleator proteins
inferredcites →https://doi.org/10.1017/cbo9780511675997.006openalex-snapshot
Cell structural modifications in insects at low temperatures
inferredcites →https://doi.org/10.1017/s0016672310000108openalex-snapshot
Genetic variation insenescence marker protein-30is associated with natural variation in cold tolerance inDrosophila
inferredcites →https://doi.org/10.1017/s1464793102006024openalex-snapshot
Climatic variability and the evolution of insect freeze tolerance
inferredcites →https://doi.org/10.1038/25147openalex-snapshot
Calcium promotes cell survival through CaM-K kinase activation of the protein-kinase-B pathway
inferredcites →https://doi.org/10.1038/sj.embor.7400072openalex-snapshot
Involvement of ASK1 in Ca2+‐induced p38 MAP kinase activation
inferredcites →https://doi.org/10.1073/pnas.0703538104openalex-snapshot
Up-regulation of heat shock proteins is essential for cold survival during insect diapause
inferredcites →https://doi.org/10.1073/pnas.0805041105openalex-snapshot
Distinct TRP channels are required for warm and cool avoidance in Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.082580699openalex-snapshot
Supercool or dehydrate? An experimental analysis of overwintering strategies in small permeable arctic invertebrates
inferredcites →https://doi.org/10.1073/pnas.0909872106openalex-snapshot
A nonprotein thermal hysteresis-producing xylomannan antifreeze in the freeze-tolerant Alaskan beetle Upis ceramboides
inferredcites →https://doi.org/10.1073/pnas.1007075107openalex-snapshot
Mechanisms of suspended animation are revealed by transcript profiling of diapause in the flesh fly
inferredcites →https://doi.org/10.1073/pnas.1107060108openalex-snapshot
Hyperprolinemic larvae of the drosophilid fly, Chymomyza costata , survive cryopreservation in liquid nitrogen
inferredcites →https://doi.org/10.1073/pnas.1119986109openalex-snapshot
Conversion of the chill susceptible fruit fly larva ( Drosophila melanogaster ) to a freeze tolerant organism
inferredcites →https://doi.org/10.1073/pnas.1212788109openalex-snapshot
Reestablishment of ion homeostasis during chill-coma recovery in the cricket Gryllus pennsylvanicus
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/10.1074/jbc.m005552200openalex-snapshot
Regulation of Aquaporin-2 Trafficking by Vasopressin in the Renal Collecting Duct
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/jmedent/43.4.713openalex-snapshot
Enhanced Cold and Desiccation Tolerance in Diapausing Adults of Culex pipiens, and a Role for Hsp70 in Response to Cold Shock but Not as a Component of the Diapause Program
inferredcites →https://doi.org/10.1096/fasebj.6.6.1544539openalex-snapshot
Glycogen phosphorylase: control by phosphorylation and allosteric effectors
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.1365-2583.2007.00739.xopenalex-snapshot
Gene transcription during exposure to, and recovery from, cold and desiccation stress in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-2583.2011.01119.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.1365-3032.1985.tb00052.xopenalex-snapshot
Cold tolerance in diapausing and non‐diapausing stages of the flesh fly, Sarcophaga crassipalpis
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.1365-3032.2009.00677.xopenalex-snapshot
Hardening trumps acclimation in improving cold tolerance of Drosophila melanogaster larvae
inferredcites →https://doi.org/10.1126/science.1165712openalex-snapshot
Changes in Temperature Preferences and Energy Homeostasis in Dystroglycan Mutants
inferredcites →https://doi.org/10.1126/science.238.4832.1415openalex-snapshot
A Rapid Cold-Hardening Process in Insects
inferredcites →https://doi.org/10.1139/z2012-011openalex-snapshot
Insect cold hardiness: metabolic, gene, and protein adaptation 1 This review is part of a virtual symposium on recent advances in understanding a variety of complex regulatory processes in insect physiology and endocrinology, including development, metabolism, cold hardiness, food intake and…
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.571openalex-snapshot
PLANT COLD ACCLIMATION: Freezing Tolerance Genes and Regulatory Mechanisms
inferredcites →https://doi.org/10.1146/annurev.en.06.010161.000415openalex-snapshot
Principles of Insect Cold-Hardiness
inferredcites →https://doi.org/10.1146/annurev.physiol.60.1.619openalex-snapshot
THE MITOCHONDRIAL DEATH/LIFE REGULATOR IN APOPTOSIS AND NECROSIS
inferredcites →https://doi.org/10.1146/annurev.physiol.61.1.243openalex-snapshot
HEAT-SHOCK PROTEINS, MOLECULAR CHAPERONES, AND THE STRESS RESPONSE: Evolutionary and Ecological Physiology
inferredcites →https://doi.org/10.1146/annurev.physiol.63.1.327openalex-snapshot
Antifreeze and Ice Nucleator Proteins in Terrestrial Arthropods
inferredcites →https://doi.org/10.1146/annurev.pp.35.060184.002551openalex-snapshot
Role of the Plasma Membrane in Freezing Injury and Cold Acclimation
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/physiolgenomics.00042.2012openalex-snapshot
Combined transcriptomic and metabolomic approach uncovers molecular mechanisms of cold tolerance in a temperate flesh fly
inferredcites →https://doi.org/10.1186/1471-2164-10-234openalex-snapshot
Gene discovery using massively parallel pyrosequencing to develop ESTs for the flesh fly Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1210/edrv.22.2.0428openalex-snapshot
Mitogen-Activated Protein (MAP) Kinase Pathways: Regulation and Physiological Functions*
inferredcites →https://doi.org/10.1210/er.22.2.153openalex-snapshot
Mitogen-Activated Protein (MAP) Kinase Pathways: Regulation and Physiological Functions
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.00923openalex-snapshot
On the nature of pre-freeze mortality in insects: water balance, ion homeostasis and energy charge in the adults ofPyrrhocoris apterus
inferredcites →https://doi.org/10.1242/jeb.011874openalex-snapshot
Cryoprotective dehydration and the resistance to inoculative freezing in the Antarctic midge, Belgica antarctica
inferredcites →https://doi.org/10.1242/jeb.01320openalex-snapshot
Partial link between the seasonal acquisition of cold-tolerance and desiccation resistance in the goldenrod gall flyEurosta solidaginis(Diptera: Tephritidae)
inferredcites →https://doi.org/10.1242/jeb.016758openalex-snapshot
Aquaporins play a role in desiccation and freeze tolerance in larvae of the goldenrod gall fly, Eurosta solidaginis
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.01730openalex-snapshot
Organic osmolytes as compatible, metabolic and counteracting cytoprotectants in high osmolarity and other stresses
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.02484openalex-snapshot
Seasonal acquisition of chill tolerance and restructuring of membrane glycerophospholipids in an overwintering insect: triggering by low temperature, desiccation and diapause progression
inferredcites →https://doi.org/10.1242/jeb.051003openalex-snapshot
Knocking down expression of Hsp22 and Hsp23 by RNA interference affects recovery from chill coma in Drosophila melanogaster
inferredcites →https://doi.org/10.1242/jeb.061085openalex-snapshot
Developmental trajectories of gene expression reveal candidates for diapause termination: a key life-history transition in the apple maggot flyRhagoletis pomonella
inferredcites →https://doi.org/10.1242/jeb.069948openalex-snapshot
Myo-inositol as a main metabolite in overwintering flies: seasonal metabolomic profiles and cold stress tolerance in a northern drosophilid fly
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.199.2.465openalex-snapshot
Fat Body Cells and Calcium Phosphate Spherules Induce Ice Nucleation in the Freeze-Tolerant Larvae of the Gall Fly Eurosta Solidaginis (Diptera, Tephritidae)
inferredcites →https://doi.org/10.1242/jeb.199.7.1483openalex-snapshot
Oxidative Stress and Antioxidants in Overwintering Larvae of Cold-Hardy Goldenrod Gall Insects
inferredcites →https://doi.org/10.1242/jeb.200.1.185openalex-snapshot
Modeling Seasonal Changes in Intracellular Freeze-Tolerance of Fat Body Cells of the Gall Fly Eurosta Solidaginis (Diptera, Tephritidae)
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/10.1371/journal.pone.0025025openalex-snapshot
Long-Term Cold Acclimation Extends Survival Time at 0°C and Modifies the Metabolomic Profiles of the Larvae of the Fruit Fly Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pone.0032606openalex-snapshot
Metabolic and Proteomic Profiling of Diapause in the Aphid Parasitoid Praon volucre
inferredcites →https://doi.org/10.5281/zenodo.10767265openalex-snapshot
Increased dietary cholesterol enhances cold tolerance in Drosophila melanogaster.
inferredcites →https://doi.org/10.5860/choice.36-4481openalex-snapshot
Temperature sensitivity in insects and application in integrated pest management
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.21831openalex-snapshot
Expression stability of candidate RT‐qPCR housekeeping genes in Spodoptera frugiperda (Lepidoptera: Noctuidae)
inferred← citeshttps://doi.org/10.1002/arch.21861openalex-snapshot
Glycerol biosynthesis plays an essential role in mediating cold tolerance the red imported fire ant,Solenopsis invicta
inferred← citeshttps://doi.org/10.1002/arch.70126openalex-snapshot
Thermal Stress‐Induced Metabolic Shifts in the Parthenium Beetle: An Untargeted Metabolomics Study
inferred← citeshttps://doi.org/10.1002/arch.70188openalex-snapshot
Transcriptomic and Proteomic Insights Into Diapause in the Wheat Stink Bug, Aelia rostrata
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/10.1002/ece3.11511openalex-snapshot
Bigger isn't always better: Challenging assumptions about the associations between diapause, body weight, and overwintering survival
inferred← citeshttps://doi.org/10.1002/ece3.2792openalex-snapshot
Differential expression patterns of two delta‐9‐acyl‐CoA desaturases in Thitarodes pui (Lepidoptera: Hepialidae) during different seasons and cold exposure
inferred← citeshttps://doi.org/10.1002/ece3.3112openalex-snapshot
Seasonal variation in basal and plastic cold tolerance: Adaptation is influenced by both long‐ and short‐term phenotypic plasticity
inferred← citeshttps://doi.org/10.1002/ece3.4945openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ece3.5887openalex-snapshot
Phenotypic plasticity, but not adaptive tracking, underlies seasonal variation in post‐cold hardening freeze tolerance of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1002/ece3.6410openalex-snapshot
Transcriptome analysis of Drosophila melanogaster laboratory strains of different geographical origin after long‐term laboratory maintenance
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Seasonal polyphenism of spotted‐wing Drosophila is affected by variation in local abiotic conditions within its invaded range, likely influencing survival and regional population dynamics
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Winter Temperature Affects Fatty Acid Composition and Gene Expression, but Not Fat Content and Survival in a Northern Population of a Range‐Expanding Spider
inferred← citeshttps://doi.org/10.1002/ece3.73321openalex-snapshot
Different Transcriptional Responses to Developmental Versus Short‐Term Acclimation Temperatures in Pieris rapae
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Cold stress results in sustained locomotor and behavioral deficits in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1002/jez.2502openalex-snapshot
The amino acid and lipophilic profiles of Chilo partellus (Swinhoe) larvae fluctuate with diapause
inferred← citeshttps://doi.org/10.1002/jez.2774openalex-snapshot
Diapause‐induced shift in the content of major carbohydrates in Chilo partellus (Swinhoe)
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Thermal plasticity potentially mediates the interaction between host Chilo partellus Swinhoe (Lepidoptera: Crambidae) and endoparasitoid Cotesia flavipes Cameron (Hymenoptera: Braconidae) in rapidly changing environments
inferred← citeshttps://doi.org/10.1002/ps.6006openalex-snapshot
Cold hardiness of the South American tomato pinworm Tuta absoluta (Lepidoptera: Gelechiidae): both larvae and adults are chill‐susceptible
inferred← citeshttps://doi.org/10.1002/ps.7191openalex-snapshot
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Insect Lipids: Structure, Classification and Function
inferred← citeshttps://doi.org/10.1007/s00114-018-1584-7openalex-snapshot
Microbiota disruption leads to reduced cold tolerance in Drosophila flies
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Characterization of drought-induced rapid cold-hardening in the Antarctic midge, Belgica antarctica
inferred← citeshttps://doi.org/10.1007/s00300-021-02807-6openalex-snapshot
Thermal adaptations of adults and eggs in the Arctic seed bug Nysius groenlandicus (Insecta: Hemiptera) from South Greenland
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Daily thermal fluctuations to a range of subzero temperatures enhance cold hardiness of winter-acclimated turtles
inferred← citeshttps://doi.org/10.1007/s00442-025-05822-0openalex-snapshot
Seasonal variation rather than ectoparasitic fungi infection affects hemolymph parameters, thermal stress tolerance, and movement performance of an invasive ladybird
inferred← citeshttps://doi.org/10.1007/s10340-016-0741-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10340-023-01741-2openalex-snapshot
Insect resilience: unraveling responses and adaptations to cold temperatures
inferred← citeshttps://doi.org/10.1007/s10340-025-01887-1openalex-snapshot
Effects of acclimation on the cold tolerance of the pepper weevil
inferred← citeshttps://doi.org/10.1007/s10340-025-01921-2openalex-snapshot
Tissue-specific transcriptome followed by RNAi elucidates the functional roles of phenoloxidase and gustatory receptor in Bactrocera dorsalis to cold and heat stress
inferred← citeshttps://doi.org/10.1007/s10493-014-9803-1openalex-snapshot
Rapid cold hardening response in the predatory mite Neoseiulus californicus
inferred← citeshttps://doi.org/10.1007/s10493-020-00570-7openalex-snapshot
Effects of thermal shock on the survival and reproduction of Stratiolaelaps scimitus (Mesostigmata: Laelapidae)
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/s10493-025-01074-yopenalex-snapshot
Physiological reprogramming during cold acclimation in the predatory mite Neoseiulus bicaudus
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/10.1007/s11676-026-02049-4openalex-snapshot
Unveiling the secrets of Dioryctria sylvestrella: population dynamics, natural enemy resources and key regulatory factors
inferred← citeshttps://doi.org/10.1007/s11692-014-9298-zopenalex-snapshot
Disentangling the Consequences of Growth Temperature and Adult Acclimation Temperature on Starvation and Thermal Tolerance in the Red Flour Beetle
inferred← citeshttps://doi.org/10.1007/s12192-020-01147-4openalex-snapshot
Short-term cold stress and heat shock proteins in the crustacean Artemia franciscana
inferred← citeshttps://doi.org/10.1007/s13744-019-00686-5openalex-snapshot
Population Dynamics of Drosophila suzukii (Diptera: Drosophilidae) in Berry Crops in Southern Brazil
inferred← citeshttps://doi.org/10.1016/b978-0-12-409548-9.11749-xopenalex-snapshot
Cold Adaptations of Tundra Insects
inferred← citeshttps://doi.org/10.1016/b978-0-12-409548-9.11893-7openalex-snapshot
Cold Adaptations of Alpine Insects
inferred← citeshttps://doi.org/10.1016/b978-0-323-95424-2.00021-2openalex-snapshot
Insects in the cold
inferred← citeshttps://doi.org/10.1016/j.anbehav.2020.07.015openalex-snapshot
Beyond thermal melanism: association of wing melanization with fitness and flight behaviour in a butterfly
inferred← citeshttps://doi.org/10.1016/j.aqrep.2020.100453openalex-snapshot
Improving winter production of Nile tilapia: What can be done?
inferred← citeshttps://doi.org/10.1016/j.aqrep.2025.103265openalex-snapshot
Effects of acute cold and heat shocks on the protein profile of crayfish hemolymph: Implications for crustacean adaptation to thermal stress
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2017.08.028openalex-snapshot
Thermal resistance of Pacific white shrimp fed Sargassum filipendula: A MALDI-TOF mass spectrometry approach
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2019.734779openalex-snapshot
Impact of combinations of brown seaweeds on shrimp gut microbiota and response to thermal shock and white spot disease
inferred← citeshttps://doi.org/10.1016/j.aspen.2016.06.010openalex-snapshot
Do northern populations of Reticulitermes speratus (Kolbe) possess an additional physiological capacity to cold-acclimate that enhances cold tolerance during the winter?
inferred← citeshttps://doi.org/10.1016/j.aspen.2021.04.015openalex-snapshot
Metabolic dynamics across prolonged diapause development in larvae of the sawfly, Cephalcia chuxiongica (Hymenoptera: Pamphiliidae)
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.aspen.2024.102327openalex-snapshot
Hibernation changes tissue specific lipophilic profile of Chilo partellus (Swinhoe)
inferred← citeshttps://doi.org/10.1016/j.baae.2023.05.005openalex-snapshot
Suboptimal host tree benefits the overwintering of a destructive forest insect pest
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.08.008openalex-snapshot
Uncovering the benefits of fluctuating thermal regimes on cold tolerance of drosophila flies by combined metabolomic and lipidomic approach
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.118990openalex-snapshot
N-acetyltyrosine-induced redox signaling in hormesis
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2016.02.017openalex-snapshot
Phytoseiid mites under environmental stress
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2017.01.004openalex-snapshot
Cold tolerance of Trissolcus japonicus and T. cultratus, potential biological control agents of Halyomorpha halys, the brown marmorated stink bug
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2017.08.013openalex-snapshot
Cold acclimation reduces predation rate and reproduction but increases cold- and starvation tolerance in the predatory mite Gaeolaelaps aculeifer Canestrini
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2019.02.018openalex-snapshot
Interactive effects of temperature and time on cold tolerance and spring predation in overwintering soil predatory mites (Gaeolaelaps aculeifer Canestrini)
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2023.105233openalex-snapshot
Overwintering Diapause and Survival of Western Leucotaraxis Argenticollis, a Promising Biological Control Agent for Adelges Tsugae, in the Eastern United States
inferred← citeshttps://doi.org/10.1016/j.cbd.2025.101565openalex-snapshot
The molecular response of Neoseiulus bicaudus to cold acclimation
inferred← citeshttps://doi.org/10.1016/j.cbpa.2014.01.004openalex-snapshot
Dietary live yeast alters metabolic profiles, protein biosynthesis and thermal stress tolerance of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.cbpa.2015.01.007openalex-snapshot
Cold induced changes in lipid, protein and carbohydrate levels in the tropical insect Gromphadorhina coquereliana
inferred← citeshttps://doi.org/10.1016/j.cbpa.2015.11.013openalex-snapshot
Impact of different temperatures on survival and energy metabolism in the Asian citrus psyllid, Diaphorina citri Kuwayama
inferred← citeshttps://doi.org/10.1016/j.cbpa.2021.110912openalex-snapshot
Do energy reserves and cold hardiness limit winter survival of Culex pipiens?
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.2021.110995openalex-snapshot
Divergent metabolomic profiles of cold-exposed mature and immature females of tropical versus temperate Drosophila species
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.2022.111258openalex-snapshot
Adaptive changes in energy reserves and effects of body melanization on thermal tolerance in Drosophila simulans
inferred← citeshttps://doi.org/10.1016/j.cbpb.2017.11.006openalex-snapshot
“Alternative” fuels contributing to mitochondrial electron transport: Importance of non-classical pathways in the diversity of animal metabolism
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.129905openalex-snapshot
Thermal plasticity and sensitivity to insecticides in populations of an invasive beetle: Cyfluthrin increases vulnerability to extreme temperature
inferred← citeshttps://doi.org/10.1016/j.cois.2019.09.003openalex-snapshot
Adaptation to the abiotic environment in insects: the influence of variability on ecophysiology and evolutionary genomics
inferred← citeshttps://doi.org/10.1016/j.cois.2020.06.003openalex-snapshot
Evolutionary impacts of winter climate change on insects
inferred← citeshttps://doi.org/10.1016/j.cois.2023.101054openalex-snapshot
Cold-induced immune activation in chill-susceptible insects
inferred← citeshttps://doi.org/10.1016/j.cris.2022.100046openalex-snapshot
The Resilience of Polar Collembola (Springtails) in a Changing Climate
inferred← citeshttps://doi.org/10.1016/j.cris.2024.100089openalex-snapshot
Acclimation temperature influences the thermal sensitivity of injury accumulation in Folsomia candida at extreme low and high temperatures
inferred← citeshttps://doi.org/10.1016/j.cropro.2013.10.008openalex-snapshot
The first report on the winter breeding life history of Epuraea domina (Coleoptera: Nitidulidae) in a citrus grove in Jeju, Korea
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2014.07.013openalex-snapshot
Anoxic stress and rapid cold hardening enhance cold tolerance of the migratory locust
inferred← citeshttps://doi.org/10.1016/j.ecss.2025.109131openalex-snapshot
Effects of salinity on desiccation resistance in supratidal beetles: Cross-tolerance or cross-susceptibility?
inferred← citeshttps://doi.org/10.1016/j.envpol.2015.03.013openalex-snapshot
Abiotic stressors and stress responses: What commonalities appear between species across biological organization levels?
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.exger.2016.02.014openalex-snapshot
Moderately lower temperatures greatly extend the lifespan of Brachionus manjavacas (Rotifera): Thermodynamics or gene regulation?
inferred← citeshttps://doi.org/10.1016/j.ibmb.2015.05.012openalex-snapshot
Shifts in metabolomic profiles of the parasitoid Nasonia vitripennis associated with elevated cold tolerance induced by the parasitoid's diapause, host diapause and host diet augmented with proline
inferred← citeshttps://doi.org/10.1016/j.ibmb.2016.11.007openalex-snapshot
Cold acclimation allows Drosophila flies to maintain mitochondrial functioning under cold stress
inferred← citeshttps://doi.org/10.1016/j.ibmb.2019.01.006openalex-snapshot
Larvae of Drosophila melanogaster exhibit transcriptional activation of immune response pathways and antimicrobial peptides during recovery from supercooling stress
inferred← citeshttps://doi.org/10.1016/j.ibmb.2021.103548openalex-snapshot
Sestrin regulates acute chill coma recovery in Drosophila melanogaster
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2014.08.005openalex-snapshot
Host diapause status and host diets augmented with cryoprotectants enhance cold hardiness in the parasitoid Nasonia vitripennis
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2015.03.015openalex-snapshot
Chill-tolerant Gryllus crickets maintain ion balance at low temperatures
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2015.03.016openalex-snapshot
Temperate Drosophila preserve cardiac function at low temperature
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2015.05.003openalex-snapshot
Adult plasticity of cold tolerance in a continental-temperate population of Drosophila suzukii
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2015.09.001openalex-snapshot
Physiological and molecular mechanisms associated with cross tolerance between hypoxia and low temperature in Thaumatotibia leucotreta
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2016.03.006openalex-snapshot
Reproductive arrest and stress resistance in winter-acclimated Drosophila suzukii
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2016.08.006openalex-snapshot
The importance of relative humidity and trophic resources in governing ecological niche of the invasive carabid beetle Merizodus soledadinus in the Kerguelen archipelago
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2016.09.006openalex-snapshot
Chronic dietary salt stress mitigates hyperkalemia and facilitates chill coma recovery in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2016.10.008openalex-snapshot
Cold tolerance of third-instar Drosophila suzukii larvae
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2017.04.007openalex-snapshot
Elevated chaperone proteins are a feature of winter freeze avoidance by larvae of the goldenrod gall moth, Epiblema scudderiana
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2017.11.004openalex-snapshot
Effects of cold acclimation on rectal macromorphology, ultrastructure, and cytoskeletal stability in Gryllus pennsylvanicus crickets
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2018.11.003openalex-snapshot
Physiology of crapemyrtle bark scale, Acanthococcus lagerstroemiae (Kuwana), associated with seasonally altered cold tolerance
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2019.01.001openalex-snapshot
Fluctuating thermal regime preserves physiological homeostasis and reproductive capacity in Drosophila suzukii
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2019.103996openalex-snapshot
Is rapid cold-hardening an aerobic process? Characterization of changes in metabolic activity during its induction and effects of anoxia in flesh fly
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2020.104075openalex-snapshot
Drawing the line: Linear or non-linear reaction norms in response to adult acclimation on lower thermal limits
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2021.104323openalex-snapshot
Acclimation, duration and intensity of cold exposure determine the rate of cold stress accumulation and mortality in Drosophila suzukii
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2023.104488openalex-snapshot
Fat enough for the winter? Does nutritional status affect diapause?
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2023.104581openalex-snapshot
Metabolomes of bumble bees reared in common garden conditions suggest constitutive differences in energy and toxin metabolism across populations
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2023.104610openalex-snapshot
Metabolites, ions, and the mechanisms behind seasonal cold hardening of Pyrochroa coccinea (Pyrochroidae) larvae
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2024.104619openalex-snapshot
Plasticity of cold and heat stress tolerance induced by hardening and acclimation in the melon thrips
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.jinsphys.2025.104864openalex-snapshot
Pitfalls in insect cryoprotectant functional studies: A case study of myo-inositol in Drosopila lummei
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2026.105013openalex-snapshot
Cold survival in aphids: linking species-specific metabolic responses to cold tolerance
inferred← citeshttps://doi.org/10.1016/j.jspr.2026.102989openalex-snapshot
Aphagy under pressure: Cold unveils hidden energetic conflicts across sex and generations
inferred← citeshttps://doi.org/10.1016/j.jspr.2026.103130openalex-snapshot
Adaptation mechanisms of Cheyletus malaccensis (Oudemans) (Acari: Cheyletidae) under low-temperature stress: A multi-dimensional analysis of phenotype, physiology, and transcriptome
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2014.02.019openalex-snapshot
The overwintering biology of the acorn weevil, Curculio glandium in southwestern Ontario
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2015.11.003openalex-snapshot
An invitation to measure insect cold tolerance: Methods, approaches, and workflow
inferred← citeshttps://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 )
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2018.04.013openalex-snapshot
Studies on chill coma recovery in the ladybird, Harmonia axyridis: Ontogenetic profile, effect of repeated cold exposures, and capacity to predict winter survival
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2018.12.022openalex-snapshot
Changes in biochemical contents and survival rates of two stored product moths under different thermal regimes
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2020.102748openalex-snapshot
Morphological response of the red palm weevil, Rhynchophorus ferrugineus, to a transient low temperature analyzed by computer tomography and holographic microscopy
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2021.102950openalex-snapshot
Thermal tolerance variations and physiological adjustments in a winter active and a summer active aphid species
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2023.103591openalex-snapshot
Keep your cool: Overwintering physiology in response to urbanization in the acorn ant, Temnothorax curvispinosus
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2024.103992openalex-snapshot
Advances in understanding Lepidoptera cold tolerance
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.2025.104068openalex-snapshot
Acclimation effects on thermal locomotor performance of the invasive Polyphagous Shot Hole Borer beetle, Euwallacea fornicatus (Coleoptera: Curculionidae: Scolytinae)
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2025.104100openalex-snapshot
Effects of duration and type of cold acclimation on the subsequent cold tolerance of a tenebrionid beetle
inferred← citeshttps://doi.org/10.1016/j.scib.2019.09.028openalex-snapshot
L-proline feeding for augmented freeze tolerance of Camponotus japonicus Mayr
inferred← citeshttps://doi.org/10.1016/j.tree.2026.03.005openalex-snapshot
The reshaping of trade-offs under climate warming
inferred← citeshttps://doi.org/10.1017/9781108609364.002openalex-snapshot
Confronting the Challenges of a Seasonal Environment
inferred← citeshttps://doi.org/10.1017/9781108609364.003openalex-snapshot
Which Seasons Are Being Avoided?
inferred← citeshttps://doi.org/10.1017/9781108609364.004openalex-snapshot
Variation in the Diapause Response
inferred← citeshttps://doi.org/10.1017/9781108609364.005openalex-snapshot
The Cost of Diapause and Some Diapause Alternatives
inferred← citeshttps://doi.org/10.1017/9781108609364.006openalex-snapshot
Interpreting Seasonal Cues to Program Diapause Entry
inferred← citeshttps://doi.org/10.1017/9781108609364.009openalex-snapshot
Ending Diapause and Reinitiating Development
inferred← citeshttps://doi.org/10.1017/9781108609364.010openalex-snapshot
Molecular Signaling Pathways that Regulate Diapause
inferred← citeshttps://doi.org/10.1017/9781108609364.011openalex-snapshot
Genetic Control of Diapause
inferred← citeshttps://doi.org/10.1017/s0007485321000791openalex-snapshot
Harnessing thermal plasticity to enhance the performance of mass-reared insects: opportunities and challenges
inferred← citeshttps://doi.org/10.1017/s0007485321001073openalex-snapshot
Transcriptome analysis uncovers different avenues for manipulating cold performance in Chrysomya megacephala (Diptera, Calliphoridae)
inferred← citeshttps://doi.org/10.1017/s0007485323000111openalex-snapshot
Ontogenetic responses of physiological fitness in Spodoptera frugiperda (Lepidoptera: Noctuidae) in response to repeated cold exposure
inferred← citeshttps://doi.org/10.1017/s0007485323000196openalex-snapshot
Cold tolerance and overwintering survival of Aphelinus certus (Hymenoptera: Aphelinidae), a parasitoid of the soybean aphid (Hemiptera: Aphididae) in North America
inferred← citeshttps://doi.org/10.1017/s0007485323000251openalex-snapshot
Rapid cold hardening and cold acclimation promote cold tolerance of oriental fruit fly, Bactrocera dorsalis (Hendel) by physiological substances transformation and cryoprotectants accumulation
inferred← citeshttps://doi.org/10.1017/s0007485323000548openalex-snapshot
Effect of constant and fluctuating low temperature on the survival of Tuta absoluta pupae
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c03896openalex-snapshot
Glycerol Metabolism is Important for the Low-Temperature Adaptation of a Global Quarantine Pest Anoplophora glabripennis Larvae
inferred← citeshttps://doi.org/10.1021/acs.jproteome.6b00427openalex-snapshot
Quantitative Phosphoproteomics Reveals Signaling Mechanisms Associated with Rapid Cold Hardening in a Chill-Tolerant Fly
inferred← citeshttps://doi.org/10.1038/hdy.2015.6openalex-snapshot
How consistent are the transcriptome changes associated with cold acclimation in two species of the Drosophila virilis group?
inferred← citeshttps://doi.org/10.1038/s41437-020-00398-2openalex-snapshot
Sex-specific responses to cold in a very cold-tolerant, northern Drosophila species
inferred← citeshttps://doi.org/10.1038/s41437-024-00669-2openalex-snapshot
Genetic constraints in genes exhibiting splicing plasticity in facultative diapause
inferred← citeshttps://doi.org/10.1038/s41559-023-02239-xopenalex-snapshot
Temperate species underfill their tropical thermal potentials on land
inferred← citeshttps://doi.org/10.1038/s41598-017-01974-zopenalex-snapshot
Large scale phosphoprotein profiling to explore Drosophila cold acclimation regulatory mechanisms
inferred← citeshttps://doi.org/10.1038/s41598-018-22757-0openalex-snapshot
Recovery from supercooling, freezing, and cryopreservation stress in larvae of the drosophilid fly, Chymomyza costata
inferred← citeshttps://doi.org/10.1038/s41598-020-57868-0openalex-snapshot
Effects of elevational range shift on the morphology and physiology of a carabid beetle invading the sub-Antarctic Kerguelen Islands
inferred← citeshttps://doi.org/10.1038/s41598-020-68941-zopenalex-snapshot
Characterization of Gromphadorhina coquereliana hemolymph under cold stress
inferred← citeshttps://doi.org/10.1038/s41598-024-68753-5openalex-snapshot
Selection for stress tolerance and longevity in Drosophila melanogaster have strong impacts on microbiome profiles
inferred← citeshttps://doi.org/10.1038/s41598-024-79082-yopenalex-snapshot
Glucose influence cold tolerance in the fall armyworm, Spodoptera frugiperda via trehalase gene expression
inferred← citeshttps://doi.org/10.1038/s41598-026-51703-8openalex-snapshot
Contrasting epigenetics of Ixodes scapularis populations
inferred← citeshttps://doi.org/10.1038/srep28999openalex-snapshot
Cold acclimation wholly reorganizes the Drosophila melanogaster transcriptome and metabolome
inferred← citeshttps://doi.org/10.1073/pnas.1503456112openalex-snapshot
Constraints, independence, and evolution of thermal plasticity: Probing genetic architecture of long- and short-term thermal acclimation
inferred← citeshttps://doi.org/10.1073/pnas.2211744119openalex-snapshot
Stabilization of insect cell membranes and soluble enzymes by accumulated cryoprotectants during freezing stress
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/10.1080/09670874.2023.2244919openalex-snapshot
Rapid responses are essential: adaptive temporal variation in cold tolerance of the invasive fall armyworm
inferred← citeshttps://doi.org/10.1080/09670874.2023.2251024openalex-snapshot
Seasonal changes in supercooling capacity and main polyols in overwintering adults of Acrosternum millierei (Hemiptera: Pentatomidae)
inferred← citeshttps://doi.org/10.1080/19336934.2021.2016327openalex-snapshot
Adaptation and ecological speciation in seasonally varying environments at high latitudes: Drosophila virilis group
inferred← citeshttps://doi.org/10.1086/680384openalex-snapshot
Comparative Ecophysiology of Cold-Tolerance-Related Traits: Assessing Range Expansion Potential for an Invasive Insect at High Latitude
inferred← citeshttps://doi.org/10.1086/689323openalex-snapshot
Previous Repeated Exposure to Food Limitation Enables Rats to Spare Lipid Stores during Prolonged Starvation
inferred← citeshttps://doi.org/10.1093/ee/nvaf007openalex-snapshot
Cold tolerance strategy and lower temperature thresholds of Lycorma delicatula (Hemiptera: Fulgoridae) egg masses
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/ee/nvw088openalex-snapshot
Developmental Acclimation ofDrosophila suzukii(Diptera: Drosophilidae) and Its Effect on Diapause and Winter Stress Tolerance
inferred← citeshttps://doi.org/10.1093/ee/nvx090openalex-snapshot
Cold Tolerance of Pityophthorus juglandis (Coleoptera: Scolytidae) From Northern California
inferred← citeshttps://doi.org/10.1093/ee/nvx128openalex-snapshot
Physiological and Biochemical Differences in Diapausing and Nondiapausing Larvae of Eurytoma plotnikovi (Hymenoptera: Eurytomidae)
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1093/ee/nvy046openalex-snapshot
Comparative Antennal and Behavioral Responses of Summer and Winter Morph Drosophila suzukii (Diptera: Drosophilidae) to Ecologically Relevant Volatiles
inferred← citeshttps://doi.org/10.1093/ee/nvy074openalex-snapshot
Ovary Development and Cold Tolerance of the Invasive Pest Drosophila suzukii (Matsumura) in the Central Plains of Kansas, United States
inferred← citeshttps://doi.org/10.1093/ee/nvz162openalex-snapshot
Artificial Selection to a Nonlethal Cold Stress in Trogoderma variabile Shows Associations With Chronic Cold Stress and Body Size
inferred← citeshttps://doi.org/10.1093/gbe/evac087openalex-snapshot
The Spruce Budworm Genome: Reconstructing the Evolutionary History of Antifreeze Proteins
inferred← citeshttps://doi.org/10.1093/gbe/evaf077openalex-snapshot
Navigating the Cold: Integrative Transcriptome Sequencing Approach Reveals Ionoregulatory and Whole-Body Responses to Cold Acclimation in Drosophila ananassae
inferred← citeshttps://doi.org/10.1093/gbe/evag101openalex-snapshot
Examining the Role of a Chromosomal Inversion in Accumulating Adaptive and Barrier Loci in a Cold-adapted Insect Species
inferred← citeshttps://doi.org/10.1093/glycob/cwad011openalex-snapshot
Regulation of trehalose metabolism in insects: from genes to the metabolite window
inferred← citeshttps://doi.org/10.1093/icb/icaf085openalex-snapshot
A Systems Approach to Homeostasis: What Euryhaline Fish Teach Us About Organismal Stress Responses
inferred← citeshttps://doi.org/10.1093/icb/icx102openalex-snapshot
Genetic Decoupling of Thermal Hardiness across Metamorphosis in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1093/icb/icz126openalex-snapshot
Thermoprofile Parameters Affect Survival of Megachile rotundata During Exposure to Low-Temperatures
inferred← citeshttps://doi.org/10.1093/jee/toae137openalex-snapshot
Cold tolerance and metabolism of red-haired pine bark beetle Hylurgus ligniperda (Coleoptera: Curculionidae) during the overwintering period
inferred← citeshttps://doi.org/10.1093/jee/toag273openalex-snapshot
Why does the effectiveness of light trapping for tea leafhoppers decline sharply in late autumn?
inferred← citeshttps://doi.org/10.1093/jee/toag300openalex-snapshot
Post-harvest treatments to reduce emergence and damage caused by larvae of Curculio sayi (Coleoptera: Curculionidae)
inferred← citeshttps://doi.org/10.1093/jisesa/ieac025openalex-snapshot
Comparative Transcriptome Analysis Reveals Molecular Insights in Overwintering Monochamus alternatus (Coleoptera: Cerambycidae)
inferred← citeshttps://doi.org/10.1093/jisesa/ieaf103openalex-snapshot
Exploration of real-time fluorescence quantitative PCR by analyzing effective reference genes in Galleria mellonella (Lepidoptera: Pyralidae)
inferred← citeshttps://doi.org/10.1093/jisesa/ieaf109openalex-snapshot
Cold adaptation mechanism in Bactrocera dorsalis (Diptera: Tephritidae) by regulating MAPK signaling and metabolic pathways
inferred← citeshttps://doi.org/10.1093/jisesa/ieag064openalex-snapshot
Transcriptomic responses of red palm weevil (Coleoptera: Curculionidae) larvae to low-temperature exposure
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