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Diapause induction as an interplay between seasonal token stimuli, and modifying and directly limiting factors: hibernation in Chymomyza costata
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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/(sici)1520-6327(199910)42:2<147::aid-arch5>3.0.co;2-xopenalex-snapshot
Dopamine and serotonin in the larval CNS of a drosophilid fly,Chymomyza costata: Are they involved in the regulation of diapause?
inferredcites →https://doi.org/10.1007/bf00188113openalex-snapshot
Photoperiodism and thermoperiodism in the predatory mite Amblyseius potentillae are probably based on the same mechanism
inferredcites →https://doi.org/10.1007/bf01951676openalex-snapshot
Thermoperiodically induced diapause in a mite in constant darkness is vitamin A dependent
inferredcites →https://doi.org/10.1016/0022-1910(66)90095-3openalex-snapshot
Larval diapause of maternal origin—II. The effect of photoperiod and temperature on Nasonia vitripennis
inferredcites →https://doi.org/10.1016/0022-1910(68)90060-7openalex-snapshot
Photoperiodism and time measurement in the parasitic wasp, Nasonia vitripennis
inferredcites →https://doi.org/10.1016/0022-1910(82)90087-7openalex-snapshot
Thermoperiodic induction of larval diapause in the European corn borer, Ostrinia nubilalis
inferredcites →https://doi.org/10.1016/0022-1910(85)90040-xopenalex-snapshot
Effects of thermoperiod on photoperiodic determination of larval diapause in Ostrinia nubilalis
inferredcites →https://doi.org/10.1016/0022-1910(87)90055-2openalex-snapshot
Thermoperiod-photoperiod interactions in the determination of diapause in Ostrinia nubilalis
inferredcites →https://doi.org/10.1016/0022-1910(88)90137-0openalex-snapshot
Thermoperiodic induction of diapause in the predacious mite, Amblyseius potentillae
inferredcites →https://doi.org/10.1016/0022-1910(92)90033-aopenalex-snapshot
Weak circadian eclosion rhythmicity in Chymomyza costata (Diptera: Drosophilidae), and its independence of diapause type
inferredcites →https://doi.org/10.1016/0022-1910(94)00117-yopenalex-snapshot
The photoperiodic clock in Chymomyza costata
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.cois.2014.12.002openalex-snapshot
Photoperiodic time measurement in insects
inferredcites →https://doi.org/10.1016/j.cub.2005.06.056openalex-snapshot
Temperature Synchronization of the Drosophila Circadian Clock
inferredcites →https://doi.org/10.1016/j.cub.2012.12.023openalex-snapshot
Cryptochrome Antagonizes Synchronization of Drosophila’s Circadian Clock to Temperature Cycles
inferredcites →https://doi.org/10.1016/j.jinsphys.2005.09.008openalex-snapshot
Eco-physiological phases of insect diapause
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.10.006openalex-snapshot
Insect photoperiodic calendar and circadian clock: Independence, cooperation, or unity?
inferredcites →https://doi.org/10.1016/j.neuron.2009.08.026openalex-snapshot
Temperature Entrainment of Drosophila's Circadian Clock Involves the Gene nocte and Signaling from Peripheral Sensory Tissues to the Brain
inferredcites →https://doi.org/10.1016/j.tig.2009.03.009openalex-snapshot
Complications of complexity: integrating environmental, genetic and hormonal control of insect diapause
inferredcites →https://doi.org/10.1016/s0022-1910(01)00113-5openalex-snapshot
Malfunction of circadian clock in the non-photoperiodic-diapause mutants of the drosophilid fly, Chymomyza costata
inferredcites →https://doi.org/10.1016/s0022-1910(96)00094-7openalex-snapshot
Effects of Temperature on Weak Circadian Eclosion Rhythmicity in Chymomyza costata (Diptera: Drosophilidae)
inferredcites →https://doi.org/10.1016/s0022-1910(98)00043-2openalex-snapshot
Developmental changes in dopamine levels in larvae of the fly Chymomyza costata: comparison between wild-type and mutant-nondiapause strains
inferredcites →https://doi.org/10.1016/s0022-1910(99)00124-9openalex-snapshot
Induction and development of winter larval diapause in a drosophilid fly, Chymomyza costata
inferredcites →https://doi.org/10.1016/s0022-1910(99)00195-xopenalex-snapshot
Circadian component influences the photoperiodic induction of diapause in a drosophilid fly, Chymomyza costata
inferredcites →https://doi.org/10.1038/hdy.1983.39openalex-snapshot
Stopped development in overcrowded cultures of Drosophila melanogaster
inferredcites →https://doi.org/10.1038/nature16148openalex-snapshot
Drosophila Ionotropic Receptor 25a mediates circadian clock resetting by temperature
inferredcites →https://doi.org/10.1086/282327openalex-snapshot
The Entrainment of Circadian Oscillations by Light and Their Role as Photoperiodic Clocks
inferredcites →https://doi.org/10.1093/aesa/49.3.303openalex-snapshot
The Physiology of Diapause in Arthropods
inferredcites →https://doi.org/10.1093/aob/mcr215openalex-snapshot
Photoperiodism. The biological calendar
inferredcites →https://doi.org/10.1101/sqb.1960.025.01.026openalex-snapshot
Circadian Rhythms and the Time Measurement in Photoperiodism
inferredcites →https://doi.org/10.1111/ens.12000openalex-snapshot
Roles of circadian clock genes in insect photoperiodism
inferredcites →https://doi.org/10.1111/j.1365-3032.1988.tb01128.xopenalex-snapshot
A mutant strain of Chymomyza costata (Diptera: Drosophilidae) insensitive to diapause‐inducing action of photoperiod
inferredcites →https://doi.org/10.1111/j.1365-3032.1997.tb01165.xopenalex-snapshot
Under‐sized larvae from short‐day adults of the blow fly, Calliphora vicina , side‐step the diapause programme
inferredcites →https://doi.org/10.1111/j.1365-3032.2004.0369.xopenalex-snapshot
Photoperiodic induction of diapause: opening the black box
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04295.xopenalex-snapshot
Temperature cycles drive Drosophila circadian oscillation in constant light that otherwise induces behavioural arrhythmicity
inferredcites →https://doi.org/10.1111/j.1570-7458.1988.tb02486.xopenalex-snapshot
Multiple role of temperature during insect diapause: a review
inferredcites →https://doi.org/10.1111/j.1601-5223.1989.tb00780.xopenalex-snapshot
Genetics of the photoperiodic larval diapause in Chymomyza costata (Diptera; Drosophilidae)
inferredcites →https://doi.org/10.1111/phen.12131openalex-snapshot
The temporal ‘structure’ and function of the insect photoperiodic clock: a tribute to Colin S. Pittendrigh
inferredcites →https://doi.org/10.1126/science.181.4097.358openalex-snapshot
Thermoperiodic Control of Diapause in an Insect: Theory of Internal Coincidence
inferredcites →https://doi.org/10.1126/science.270.5237.805openalex-snapshot
Positional Cloning and Sequence Analysis of the Drosophila Clock Gene, timeless
inferredcites →https://doi.org/10.1126/science.8128246openalex-snapshot
Loss of Circadian Behavioral Rhythms and per RNA Oscillations in the Drosophila Mutant timeless
inferredcites →https://doi.org/10.1146/annurev.en.21.010176.000501openalex-snapshot
Insect Seasonality: Diapause Maintenance, Termination, and Postdiapause Development
inferredcites →https://doi.org/10.1146/annurev.en.28.010183.000515openalex-snapshot
Insect Thermoperiodism
inferredcites →https://doi.org/10.1146/annurev.en.31.010186.001323openalex-snapshot
Dormancy in Tropical Insects
inferredcites →https://doi.org/10.1146/annurev.ento.47.091201.145137openalex-snapshot
Regulation of Diapause
inferredcites →https://doi.org/10.1146/annurev.es.19.110188.000245openalex-snapshot
INSECT SEASONALITY: WHY?
inferredcites →https://doi.org/10.1163/156854294x00114openalex-snapshot
Photoperiodic and Thermoperiodic Control of Diapause in Plant-Inhabiting Mites: a Review
inferredcites →https://doi.org/10.1177/0748730407313364openalex-snapshot
Photoperiodic Induction of Diapause Requires Regulated Transcription of timeless in the Larval Brain of Chymomyza costata
inferredcites →https://doi.org/10.1177/0748730410365656openalex-snapshot
What Season Is It Anyway? Circadian Tracking vs. Photoperiodic Anticipation in Insects
inferredcites →https://doi.org/10.1177/0748730410385283openalex-snapshot
Functional Molecular Analysis of a Circadian Clock Gene timeless Promoter from the Drosophilid Fly Chymomyza costata
inferredcites →https://doi.org/10.1177/0748730415627037openalex-snapshot
dTRPA1 in Non-circadian Neurons Modulates Temperature-dependent Rhythmic Activity in Drosophila melanogaster
inferredcites →https://doi.org/10.1177/074873049300800106openalex-snapshot
Behavior in Light-Dark Cycles of Drosophila Mutants That Are Arrhythmic, Blind, or Both
inferredcites →https://doi.org/10.1186/s40851-014-0003-yopenalex-snapshot
Common features in diverse insect clocks
inferredcites →https://doi.org/10.1186/s40851-014-0004-xopenalex-snapshot
Did homeobox gene duplications contribute to the Cambrian explosion?
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/10.1371/journal.pgen.1004603openalex-snapshot
Role for Circadian Clock Genes in Seasonal Timing: Testing the Bünning Hypothesis
inferredcites →https://doi.org/10.14411/eje.2003.041openalex-snapshot
TIMELESS: A link between fly's circadian and photoperiodic clocks?
inferredcites →https://doi.org/10.4039/ent111431-4openalex-snapshot
DENSITY-DEPENDENT INDUCTION OF DIAPAUSE IN THE CODLING MOTH, LASPEYRESIA POMONELLA (LEPIDOPTERA: OLETHREUTIDAE)
inferredcites →https://doi.org/10.4039/ent117135-1openalex-snapshot
HABITAT STRUCTURE OF A DROSOPHILID COMMUNITY AT INUVIK, NWT, CANADA (DIPTERA: DROSOPHILIDAE)
inferredcites →https://doi.org/10.5281/zenodo.10736905openalex-snapshot
Larval diapause induced by crowding in Chymomyza costata (Diptera: Drosophilidae).
inferredcites →https://doi.org/10.5281/zenodo.10741286openalex-snapshot
Photoperiodism and seasonal development of insects.
inferredcites →https://doi.org/10.5281/zenodo.10743935openalex-snapshot
Larval Diapause in Chymomyza costata (Diptera: Drosophilidae) I. Effects of Temperature and Photoperiod on the Development.
inferredcites →https://doi.org/10.5281/zenodo.10747709openalex-snapshot
On the biology and karyology of Chymomyza costata Zetterstedt, with reference to the taxonomy and distribution of various species of Chymomyza (Dipt., Drosophilidae).
inferredcites →https://doi.org/10.5281/zenodo.10754122openalex-snapshot
Malt as a culture medium for Drosophila species.
inferredcites →https://doi.org/10.5281/zenodo.10767146openalex-snapshot
Genetic Linkage Analysis of Photoperiodic Clock Genes in Chymomyza costata (Diptera: Drosophilidae).
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-3-030-41929-5_6openalex-snapshot
Insect Antifreeze Proteins
inferred← citeshttps://doi.org/10.1007/s00359-024-01707-4openalex-snapshot
Characterization of pre-diapause phase in the northern Drosophila species D. ezoana
inferred← citeshttps://doi.org/10.1016/j.cub.2019.09.032openalex-snapshot
Life at High Latitudes Does Not Require Circadian Behavioral Rhythmicity under Constant Darkness
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.2024.104654openalex-snapshot
Influence of temperature on the photoperiodic time measurement and on the maternal induction of diapause in Trichogramma telengai: the separation of the two effects
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2025.104904openalex-snapshot
Chromosomal influence on variation in the timing of diapause termination in Cydia pomonella
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/10.1038/s41598-018-22757-0openalex-snapshot
Recovery from supercooling, freezing, and cryopreservation stress in larvae of the drosophilid fly, Chymomyza costata
inferred← citeshttps://doi.org/10.1073/pnas.1707281114openalex-snapshot
Conceptual framework of the eco-physiological phases of insect diapause development justified by transcriptomic profiling
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/10.1098/rspb.2019.2019openalex-snapshot
Transcriptional analysis of insect extreme freeze tolerance
inferred← citeshttps://doi.org/10.1101/2023.01.23.524574openalex-snapshot
Novel pipeline for large-scale comparative population genetics Pipeline for population genetics
inferred← citeshttps://doi.org/10.1111/jen.12981openalex-snapshot
Photoperiod‐independent diapause‐inducing thermal response of Trichogramma larvae: Pattern and mechanisms
inferred← citeshttps://doi.org/10.1111/phen.12335openalex-snapshot
Diapause induction in Eotetranychus smithi (Acari: Tetranychidae): effect of average temperature, but not of thermoperiod
inferred← citeshttps://doi.org/10.1242/jeb.170464openalex-snapshot
Thermal analysis of ice and glass transitions in insects that do and do not survive freezing
inferred← citeshttps://doi.org/10.1242/jeb.189647openalex-snapshot
Insect fat body cell morphology and response to cold stress is modulated by acclimation
inferred← citeshttps://doi.org/10.1242/jeb.246456openalex-snapshot
Mortality caused by extracellular freezing is associated with fragmentation of nuclear DNA in larval haemocytes of two drosophilid flies
inferred← citeshttps://doi.org/10.1371/journal.pone.0203015openalex-snapshot
Evidence that microRNAs are part of the molecular toolkit regulating adult reproductive diapause in the mosquito, Culex pipiens
inferred← citeshttps://doi.org/10.3389/fphys.2019.01288openalex-snapshot
Changes in Energy Metabolism Trigger Pupal Diapause Transition of Bactrocera minax After 20-Hydroxyecdysone Application
inferred← citeshttps://doi.org/10.3390/insects11090629openalex-snapshot
Diapause Regulation in Newly Invaded Environments: Termination Timing Allows Matching Novel Climatic Constraints in the Box Tree Moth, Cydalima perspectalis (Lepidoptera: Crambidae)
inferred← citeshttps://doi.org/10.3390/insects13080720openalex-snapshot
Gradually Increasing the Temperature Reduces the Diapause Termination Time of Trichogramma dendrolimi While Increasing Parasitoid Performance
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