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The capacity to maintain ion and water homeostasis underlies interspecific variation in Drosophila cold tolerance
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4757-0190-6_2openalex-snapshot
Principles of Insect Low Temperature Tolerance
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Characterization of optimized Na+ and Cl− liquid membranes for use with extracellular, self-referencing microelectrodes
inferredcites →https://doi.org/10.1016/0300-9629(74)90619-7openalex-snapshot
The resting potential of cockroach muscle membrane
inferredcites →https://doi.org/10.1016/j.cbpa.2006.12.033openalex-snapshot
Insect cold tolerance and repair of chill-injury at fluctuating thermal regimes: Role of ion homeostasis
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.2004.01.004openalex-snapshot
Inorganic ions in cold-hardiness
inferredcites →https://doi.org/10.1016/j.jinsphys.2004.05.004openalex-snapshot
Dissecting chill coma recovery as a measure of cold resistance: evidence for a biphasic response 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.2005.10.007openalex-snapshot
The Malpighian tubule: Rapid insights from post-genomic biology
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.2013.07.008openalex-snapshot
Feeding impairs chill coma recovery in the migratory locust (Locusta migratoria)
inferredcites →https://doi.org/10.1016/j.jinsphys.2014.02.005openalex-snapshot
A high-throughput method of hemolymph extraction from adult Drosophila without anesthesia
inferredcites →https://doi.org/10.1016/j.jinsphys.2015.03.015openalex-snapshot
Chill-tolerant Gryllus crickets maintain ion balance at low temperatures
inferredcites →https://doi.org/10.1016/s0022-1910(99)00148-1openalex-snapshot
Flight muscle resting potential and species-specific differences in chill-coma
inferredcites →https://doi.org/10.1016/s0065-2806(08)00001-5openalex-snapshot
Insect Excretory Mechanisms
inferredcites →https://doi.org/10.1038/416389aopenalex-snapshot
Ecological responses to recent climate change
inferredcites →https://doi.org/10.1038/nature01286openalex-snapshot
A globally coherent fingerprint of climate change impacts across natural systems
inferredcites →https://doi.org/10.1046/j.1365-2435.2003.07622.xopenalex-snapshot
Physiological diversity: listening to the large‐scale signal
inferredcites →https://doi.org/10.1073/pnas.1207553109openalex-snapshot
Upper thermal limits of Drosophila are linked to species distributions and strongly constrained phylogenetically
inferredcites →https://doi.org/10.1073/pnas.1501518112openalex-snapshot
Insect capa neuropeptides impact desiccation and cold tolerance
inferredcites →https://doi.org/10.1086/662642openalex-snapshot
The Relationship between Chill-Coma Onset and Recovery at the Extremes of the Thermal Window of Drosophila melanogaster
inferredcites →https://doi.org/10.1093/acprof:oso/9780198515494.001.0001openalex-snapshot
Insect Physiological Ecology
inferredcites →https://doi.org/10.1093/acprof:oso/9780199225941.001.0001openalex-snapshot
Ecological and Environmental Physiology of Insects
inferredcites →https://doi.org/10.1098/rsbl.2012.0601openalex-snapshot
Metabolic effects of CO 2 anaesthesia in Drosophila melanogaster
inferredcites →https://doi.org/10.1098/rspb.2000.1065openalex-snapshot
Thermal tolerance, climatic variability and latitude
inferredcites →https://doi.org/10.1098/rspb.2015.1483openalex-snapshot
Concurrent effects of cold and hyperkalaemia cause insect chilling injury
inferredcites →https://doi.org/10.1111/1365-2435.12310openalex-snapshot
How to assess Drosophila cold tolerance: chill coma temperature and lower lethal temperature are the best predictors of cold distribution limits
inferredcites →https://doi.org/10.1111/1365-2435.12568openalex-snapshot
Tropical to subpolar gradient in phospholipid composition suggests adaptive tuning of biological membrane function in drosophilids
inferredcites →https://doi.org/10.1111/gcb.12169openalex-snapshot
Upward ant distribution shift corresponds with minimum, not maximum, temperature tolerance
inferredcites →https://doi.org/10.1111/gcb.12521openalex-snapshot
Sensitivity to thermal extremes in Australian Drosophila implies similar impacts of climate change on the distribution of widespread and tropical species
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01685.xopenalex-snapshot
PHYLOGENETIC CONSTRAINTS IN KEY FUNCTIONAL TRAITS BEHIND SPECIES’ CLIMATE NICHES: PATTERNS OF DESICCATION AND COLD RESISTANCE ACROSS 95DROSOPHILASPECIES
inferredcites →https://doi.org/10.1146/annurev.ph.57.030195.000315openalex-snapshot
Thermal Adaptation in Biological Membranes: Is Homeoviscous Adaptation the Explanation?
inferredcites →https://doi.org/10.1152/ajpregu.00465.2014openalex-snapshot
Sodium distribution predicts the chill tolerance ofDrosophila melanogasterraised in different thermal conditions
inferredcites →https://doi.org/10.1152/physrev.1985.65.4.799openalex-snapshot
Physiology of cold tolerance in insects
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.01003openalex-snapshot
Organic cation transport by Malpighian tubules ofDrosophila melanogaster: application of two novel electrophysiological methods
inferredcites →https://doi.org/10.1242/jeb.01596openalex-snapshot
Changes in gut and Malpighian tubule transport during seasonal acclimatization and freezing in the gall flyEurosta solidaginis
inferredcites →https://doi.org/10.1242/jeb.051540openalex-snapshot
The role of the gut in insect chilling injury: cold-induced disruption of osmoregulation in the fall field cricket,Gryllus pennsylvanicus
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.098442openalex-snapshot
Why do insects enter and recover from chill coma? Low temperature and high extracellular potassium compromise muscle function inLocusta migratoria
inferredcites →https://doi.org/10.1242/jeb.107516openalex-snapshot
Cold-induced depolarization of insect muscle: Differing roles of extracellular K+ during acute and chronic chilling
inferredcites →https://doi.org/10.1242/jeb.115790openalex-snapshot
Parallel ionoregulatory adjustments underlie phenotypic plasticity and evolution ofDrosophilacold tolerance
inferredcites →https://doi.org/10.1242/jeb.123760openalex-snapshot
Muscle membrane potential and insect chill coma
inferredcites →https://doi.org/10.1242/jeb.197.1.421openalex-snapshot
The MalpighianC Tubules Of Drosophila Melanogaster : A Novel Phenotype For Studies Of Fluid Secretion And Its Control
inferredcites →https://doi.org/10.1242/jeb.198.8.1647openalex-snapshot
Fluid Reabsorption And Ion Transport By The Lower Malpighian Tubules Of Adult Female Drosophila
inferredcites →https://doi.org/10.1242/jeb.199.8.1857openalex-snapshot
Maintenance Of The K+ Activity Gradient in Insect Muscle Compared In Diptera and Lepidoptera: Contributions of Metabolic and Exchanger Mechanisms
inferredcites →https://doi.org/10.1242/jeb.202.11.1561openalex-snapshot
Contributions of K+:Cl− cotransport and Na+/K+-ATPase to basolateral ion transport in malpighian tubules of Drosophila melanogaster
inferredcites →https://doi.org/10.1242/jeb.203.2.405openalex-snapshot
Factors Affecting Membrane Permeability and Ionic Homeostasis in the Cold-Submerged Frog
inferredcites →https://doi.org/10.1242/jeb.204.18.3171openalex-snapshot
Mechanisms of cell survival in hypoxia and hypothermia
inferredcites →https://doi.org/10.1242/jeb.31.1.104openalex-snapshot
Active Transport of Water by the Malpighian Tubules of the Stick Insect, Dixippus Morosus (Orthoptera, Phasmidae)
inferredcites →https://doi.org/10.1242/jeb.31.2.260openalex-snapshot
Changes in the Blood Potassium Concentration of the African Migratory Locust (Locusta Migratoria Migratorioides R. & F.) During Food Deprivation, and the Effect on Neuromuscular Activity
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.7717/peerj.11openalex-snapshot
Assessing insect responses to climate change: What are we testing for? Where should we be heading?
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/10.1007/s00359-017-1191-7openalex-snapshot
Using optogenetics to assess neuroendocrine modulation of heart rate in Drosophila melanogaster larvae
inferred← citeshttps://doi.org/10.1007/s00360-021-01385-7openalex-snapshot
Body mass and sex, not local climate, drive differences in chill coma recovery times in common garden reared bumble bees
inferred← citeshttps://doi.org/10.1007/s00360-024-01537-5openalex-snapshot
Management of inorganic elements by overwintering physiology of cold hardy larvae of European corn borer (Ostrinia nubilalis, Hbn.)
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/s10522-026-10485-2openalex-snapshot
Age-dependent physiological responses and longevity in three Drosophila species with contrasting lifespans exposed to low temperature and constant darkness
inferred← citeshttps://doi.org/10.1007/s10750-026-06310-zopenalex-snapshot
Cold-induced shifts along the fast–slow continuum in Brachionus rotifers: adaptive integration of life history, reproduction, and behavior
inferred← citeshttps://doi.org/10.1007/s11829-020-09762-9openalex-snapshot
Host plant-related responses on the thermal fitness of Chilo partellus (Swinhoe) (Lepidoptera: Crambidae)
inferred← citeshttps://doi.org/10.1016/b978-0-323-95424-2.00021-2openalex-snapshot
Insects in the cold
inferred← citeshttps://doi.org/10.1016/b978-0-323-95424-2.00041-8openalex-snapshot
Insect nutritional biology
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.biocontrol.2017.12.005openalex-snapshot
Loss of coevolved basal and plastic responses to temperature may underlie trophic level host-parasitoid interactions under global change
inferred← citeshttps://doi.org/10.1016/j.cbd.2025.101614openalex-snapshot
Thermal profiling of novel and known miRNAs during cold acclimation in Aedes aegypti
inferred← citeshttps://doi.org/10.1016/j.cbpa.2017.11.005openalex-snapshot
The effect of cold acclimation on active ion transport in cricket ionoregulatory tissues
inferred← citeshttps://doi.org/10.1016/j.cbpa.2018.11.016openalex-snapshot
Loss of ion homeostasis is not the cause of chill coma or impaired dispersal in false codling moth Thaumatotibia leucotreta (Lepidoptera: Tortricidae)
inferred← citeshttps://doi.org/10.1016/j.cbpa.2019.03.015openalex-snapshot
The central nervous system and muscular system play different roles for chill coma onset and recovery in insects
inferred← citeshttps://doi.org/10.1016/j.cbpa.2020.110699openalex-snapshot
Reversing sodium differentials between the hemolymph and hindgut speeds chill coma recovery but reduces survival in the fall field cricket, Gryllus pennsylvanicus
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.cbpa.2020.110850openalex-snapshot
Cold acclimation preserves hindgut reabsorption capacity at low temperature in a chill-susceptible insect, Locusta migratoria
inferred← citeshttps://doi.org/10.1016/j.cbpa.2024.111751openalex-snapshot
Measuring insect osmoregulation in vitro: A reference guide
inferred← citeshttps://doi.org/10.1016/j.cois.2017.07.001openalex-snapshot
The essential roles of metal ions in insect homeostasis and physiology
inferred← citeshttps://doi.org/10.1016/j.cois.2021.02.015openalex-snapshot
Osmoregulatory capacity at low temperature is critical for insect cold tolerance
inferred← citeshttps://doi.org/10.1016/j.cois.2021.02.018openalex-snapshot
Updates on ion and water transport by the Malpighian tubule
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.2016.03.009openalex-snapshot
All or nothing: Survival, reproduction and oxidative balance in Spotted Wing Drosophila (Drosophila suzukii) in response to cold
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.2017.02.002openalex-snapshot
Physiological correlates of chill susceptibility in Lepidoptera
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.2020.104055openalex-snapshot
Warm periods in repeated cold stresses protect Drosophila against ionoregulatory collapse, chilling injury, and reproductive deficits
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2020.104087openalex-snapshot
Cold tolerance of the drosophila pupal parasitoid Trichopria drosophilae
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.2024.104701openalex-snapshot
Dietary potassium and cold acclimation additively increase cold tolerance in Drosophila melanogaster
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.2025.104063openalex-snapshot
The role of life stage and season in critical thermal limits of carrion beetles
inferred← citeshttps://doi.org/10.1016/j.scr.2021.102334openalex-snapshot
Decoding molecular markers and transcriptional circuitry of naive and primed states of human pluripotency
inferred← citeshttps://doi.org/10.1016/s2095-3119(17)61725-8openalex-snapshot
Characterization of two novel heat shock protein 70s and their transcriptional expression patterns in response to thermal stress in adult of Frankliniella occidentalis (Thysanoptera: Thripidae)
inferred← citeshttps://doi.org/10.1017/s0007485317001006openalex-snapshot
Cold acclimation increases cold tolerance independently of diapause programing in the bean bug, Riptortus pedestris
inferred← citeshttps://doi.org/10.1038/s41598-017-08926-7openalex-snapshot
Thermal acclimation mitigates cold-induced paracellular leak from the Drosophila gut
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/s41598-021-90401-5openalex-snapshot
Chill coma onset and recovery fail to reveal true variation in thermal performance among populations of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1038/s41598-023-48571-xopenalex-snapshot
Rapid seasonal changes in phenotypes in a wild Drosophila population
inferred← citeshttps://doi.org/10.1038/srep28999openalex-snapshot
Cold acclimation wholly reorganizes the Drosophila melanogaster transcriptome and metabolome
inferred← citeshttps://doi.org/10.1038/srep32346openalex-snapshot
Physiological basis for low-temperature survival and storage of quiescent larvae of the fruit fly Drosophila melanogaster
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/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/gerona/gly274openalex-snapshot
Reproductive Homeostasis and Senescence in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1093/icb/icw009openalex-snapshot
Adaptation to Low Temperature Exposure Increases Metabolic Rates Independently of Growth Rates
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/jee/toab263openalex-snapshot
Cold Tolerance of Immature Stages ofCeratitis capitataandBactrocera dorsalis(Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.1098/rsbl.2016.0123openalex-snapshot
Preservation of potassium balance is strongly associated with insect cold tolerance in the field: a seasonal study of Drosophila subobscura
inferred← citeshttps://doi.org/10.1098/rsbl.2017.0309openalex-snapshot
A positive genetic correlation between hypoxia tolerance and heat tolerance supports a controversial theory of heat stress
inferred← citeshttps://doi.org/10.1098/rspb.2020.1663openalex-snapshot
Hyperkalaemia, not apoptosis, accurately predicts insect chilling injury
inferred← citeshttps://doi.org/10.1098/rspb.2021.2121openalex-snapshot
A lack of repeatability creates the illusion of a trade-off between basal and plastic cold tolerance
inferred← citeshttps://doi.org/10.1098/rstb.2021.0169openalex-snapshot
Behavioural regulation of mineral salt intake in honeybees: a self-selection approach
inferred← citeshttps://doi.org/10.1101/2020.07.03.186759openalex-snapshot
Hyperkalemia, not apoptosis, accurately predicts chilling injury in individual locusts
inferred← citeshttps://doi.org/10.1101/2021.09.24.461715openalex-snapshot
A lack of repeatability creates the illusion of a trade-off between basal and plastic cold tolerance
inferred← citeshttps://doi.org/10.1101/2022.09.21.508851openalex-snapshot
Mortality without springing a leak: Locust gut epithelia do not become more permeable to fluorescent dextran and bacteria in the cold
inferred← citeshttps://doi.org/10.1101/2025.04.23.650207openalex-snapshot
Dissecting Cold Tolerance in Drosophila ananassae : A Multi-Phenotypic and Bulk Segregant Analysis
inferred← citeshttps://doi.org/10.1111/1365-2435.70379openalex-snapshot
Using thermal death time models to analyze cold stress resistance across Drosophila species
inferred← citeshttps://doi.org/10.1111/1744-7917.12466openalex-snapshot
Comparative assessment of the thermal tolerance of spotted stemborer, Chilo partellus (Lepidoptera: Crambidae) and its larval parasitoid, Cotesia sesamiae (Hymenoptera: Braconidae)
inferred← citeshttps://doi.org/10.1111/evo.14025openalex-snapshot
Distinct cold tolerance traits independently vary across genotypes inDrosophila melanogaster
inferred← citeshttps://doi.org/10.1146/annurev-physiol-022516-034142openalex-snapshot
The Integrative Physiology of Insect Chill Tolerance
inferred← citeshttps://doi.org/10.1152/ajpregu.00370.2018openalex-snapshot
Cold acclimation triggers lipidomic and metabolic adjustments in the spotted wing drosophila Drosophila suzukii (Matsumara)
inferred← citeshttps://doi.org/10.1152/jn.00324.2020openalex-snapshot
Online control of reach accuracy in mice
inferred← citeshttps://doi.org/10.1186/s12862-021-01849-yopenalex-snapshot
Multiple paths to cold tolerance: the role of environmental cues, morphological traits and the circadian clock gene vrille
inferred← citeshttps://doi.org/10.1186/s12864-017-3711-9openalex-snapshot
Effects of cold-acclimation on gene expression in Fall field cricket (Gryllus pennsylvanicus) ionoregulatory tissues
inferred← citeshttps://doi.org/10.1186/s12864-019-5745-7openalex-snapshot
Cold acclimation triggers major transcriptional changes in Drosophila suzukii
inferred← citeshttps://doi.org/10.1186/s13100-024-00328-7openalex-snapshot
Transposable elements in Drosophila montana from harsh cold environments
inferred← citeshttps://doi.org/10.1242/bio.060597openalex-snapshot
Elemental stoichiometry and insect chill tolerance: evolved and plastic changes in organismal Na+ and K+ content in Drosophila
inferred← citeshttps://doi.org/10.1242/jeb.140152openalex-snapshot
Hemolymph metabolites and osmolality are tightly linked to cold tolerance ofDrosophilaspecies: a comparative study
inferred← citeshttps://doi.org/10.1242/jeb.150813openalex-snapshot
Cold-acclimation improves chill tolerance in the migratory locust through preservation of ion balance and membrane potential
inferred← citeshttps://doi.org/10.1242/jeb.160176openalex-snapshot
CRISPR-induced null alleles show that Frost protects Drosophila melanogaster reproduction after cold exposure
inferred← citeshttps://doi.org/10.1242/jeb.165589openalex-snapshot
Critical thermal limits of bumble bees (Bombus impatiens) are marked by stereotypical behaviors and are unchanged by acclimation, age, or feeding status
inferred← citeshttps://doi.org/10.1242/jeb.168518openalex-snapshot
Cold tolerance ofDrosophilaspecies is tightly linked to epithelial K+ transport capacity of the Malpighian tubules and rectal pads
inferred← citeshttps://doi.org/10.1242/jeb.173930openalex-snapshot
Cold tolerance is linked to osmoregulatory function of the hindgut inLocusta migratoria
inferred← citeshttps://doi.org/10.1242/jeb.174904openalex-snapshot
Functional plasticity of the gut and the Malpighian tubules underlies cold acclimation and mitigates cold-induced hyperkalemia in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1242/jeb.179598openalex-snapshot
Central nervous shutdown underlies acute cold tolerance in tropical and temperateDrosophilaspecies
inferred← citeshttps://doi.org/10.1242/jeb.185884openalex-snapshot
Anti-diuretic activity of a CAPA neuropeptide can compromise Drosophila chill tolerance
inferred← citeshttps://doi.org/10.1242/jeb.190850openalex-snapshot
Effects of anoxia on ATP, water, ion and pH balance in an insect (Locusta migratoria)
inferred← citeshttps://doi.org/10.1242/jeb.191593openalex-snapshot
Dissecting cause from consequence: a systematic approach to thermal limits
inferred← citeshttps://doi.org/10.1242/jeb.213934openalex-snapshot
Maintenance of hindgut reabsorption during cold exposure is a key adaptation for Drosophila cold tolerance
inferred← citeshttps://doi.org/10.1242/jeb.214056openalex-snapshot
An impressive capacity for cold tolerance plasticity protects against ionoregulatory collapse in the disease vector, Aedes aegypti
inferred← citeshttps://doi.org/10.1242/jeb.215475openalex-snapshot
Chilling induces unidirectional solute leak through the locust gut epithelia
inferred← citeshttps://doi.org/10.1242/jeb.222190openalex-snapshot
Physiological responses of freshwater insects to salinity: molecular-, cellular- and organ-level studies
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.246306openalex-snapshot
Locust gut epithelia do not become more permeable to fluorescent dextran and bacteria in the cold
inferred← citeshttps://doi.org/10.1242/jeb.247498openalex-snapshot
The freeze-avoiding mountain pine beetle ( Dendroctonus ponderosae ) survives prolonged exposure to stressful cold by mitigating ionoregulatory collapse
inferred← citeshttps://doi.org/10.1242/jeb.250970openalex-snapshot
Chill-tolerant Drosophila species maintain electrogenic muscle membrane potential to resist cold-induced depolarization
inferred← citeshttps://doi.org/10.1242/jeb.252460openalex-snapshot
Early photoperiodic cues modulate capacity for adult cold tolerance in the yellow fever mosquito Aedes aegypti
inferred← citeshttps://doi.org/10.1534/genetics.119.302289openalex-snapshot
Physiology, Development, and Disease Modeling in the Drosophila Excretory System
inferred← citeshttps://doi.org/10.22215/etd/2019-13762openalex-snapshot
Examining the Effects of Cold on Gut Epithelial Permeability in Locusta migratoria
inferred← citeshttps://doi.org/10.22215/etd/2021-14804openalex-snapshot
Investigating a Link Between Cold Stress and Bacterial Leak from the Gut of Locusta Migratoria
inferred← citeshttps://doi.org/10.3389/fphys.2018.01427openalex-snapshot
Cold Acclimation of Trogoderma granarium Everts Is Tightly Linked to Regulation of Enzyme Activity, Energy Content, and Ion Concentration
inferred← citeshttps://doi.org/10.3389/fphys.2022.991923openalex-snapshot
Coping with global warming: Adult thermal thresholds in four pestiferous Anastrepha species determined under experimental laboratory conditions and development/survival times of immatures and adults under natural field conditions
inferred← citeshttps://doi.org/10.3390/genes9120624openalex-snapshot
Transcriptome Analysis Reveals Candidate Genes for Cold Tolerance in Drosophila ananassae
inferred← citeshttps://doi.org/10.3390/ijms222111710openalex-snapshot
Drosophila melanogaster as a Model Organism to Study Lithium and Boron Bioactivity
inferred← citeshttps://doi.org/10.3390/insects13020134openalex-snapshot
Cryoprotective Response as Part of the Adaptive Strategy of the Red Palm Weevil, Rhynchophorus ferrugineus, against Low Temperatures
inferred← citeshttps://doi.org/10.3390/insects16060557openalex-snapshot
Does Temperature Tolerance Increase in Long-Term Domesticated Frankliniella occidentalis Under Constant Temperature?
inferred← citeshttps://doi.org/10.6084/m9.figshare.14767114openalex-snapshot
Additional file 1 of Multiple paths to cold tolerance: the role of environmental cues, morphological traits and the circadian clock gene vrille
inferred← citeshttps://doi.org/10.70675/5a994d4bzf34cz4e9cz9d7fze9e062a48872openalex-snapshot
Mécanismes physiologiques sous-jacents à la plasticité de la thermotolérance chez la drosophile invasive Drosophila suzukii
inferred← citeshttps://doi.org/10.7554/elife.76010openalex-snapshot
An improved organ explant culture method reveals stem cell lineage dynamics in the adult Drosophila intestine
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