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Involvement of circadian oscillation(s) in the photoperiodic time measurement and the induction of reproductive diapause in a northern Drosophila species
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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/ece3.14openalex-snapshot
Adaptation to a seasonally varying environment: a strong latitudinal cline in reproductive diapause combined with high gene flow in Drosophila montana
inferredcites →https://doi.org/10.1007/bf00399766openalex-snapshot
Differences in measurement of day-length and photoperiodism in two stocks from subarctic and temperate climates in the Carabid beetle Pterostichus nigrita F.
inferredcites →https://doi.org/10.1007/bf01951677openalex-snapshot
Insect photoperiodism: the linden bug,Pyrrhocoris apterus, a species that measures daylength rather than nightlength
inferredcites →https://doi.org/10.1007/s004420050684openalex-snapshot
Hourglass and rhythmic components of photoperiodic time measurement in the pitcher plant mosquito, Wyeomyia smithii
inferredcites →https://doi.org/10.1016/0022-1910(73)90237-0openalex-snapshot
Photoperiodic time measurement in the aphid Megoura viciae
inferredcites →https://doi.org/10.1016/0022-1910(82)90011-7openalex-snapshot
Photoperiodic time measurement in the spider mite Tetranychus urticae: A novel concept
inferredcites →https://doi.org/10.1016/0022-1910(82)90041-5openalex-snapshot
Photoperiodic induction of pupal diapause in Sarcophaga argyrostoma: Temperature effects on circadian resonance
inferredcites →https://doi.org/10.1016/0022-1910(84)90064-7openalex-snapshot
Light-break experiments and photoperiodic time measurement in the spider mite Tetranychus urticae
inferredcites →https://doi.org/10.1016/0022-1910(88)90206-5openalex-snapshot
Photoperiodic induction of diapause in the large white butterfly, Pieris brassicae: Evidence for hourglass time measurement
inferredcites →https://doi.org/10.1016/j.jinsphys.2008.11.008openalex-snapshot
Possible involvement of distinct photoreceptors in the photoperiodic induction of diapause in the flesh fly Sarcophaga similis
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.05.002openalex-snapshot
Controversial aspects of photoperiodism in insects and mites
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.jinsphys.2011.05.018openalex-snapshot
Night-interrupting light inhibits diapause induction in the Kanzawa spider mite, Tetranychus kanzawai Kishida (Acari: Tetranychidae)
inferredcites →https://doi.org/10.1016/j.jinsphys.2012.11.003openalex-snapshot
Insect photoperiodism: Measuring the night
inferredcites →https://doi.org/10.1016/j.jinsphys.2013.02.005openalex-snapshot
Effect of temperature on the duration of sensitive period and on the number of photoperiodic cycles required for the induction of reproductive diapause in Drosophila montana
inferredcites →https://doi.org/10.1016/s0022-1910(01)00054-3openalex-snapshot
Phenotypic evolution and the genetic architecture underlying photoperiodic time measurement
inferredcites →https://doi.org/10.1016/s0022-1910(01)00106-8openalex-snapshot
Photoperiodic time measurement in insects and mites: a critical evaluation of the oscillator-clock hypothesis
inferredcites →https://doi.org/10.1016/s0022-5193(05)80195-xopenalex-snapshot
A coupled oscillator feedback system as a model for the photoperiodic clock in insects and mites. I. The basic control system as a model for circadian rhythms
inferredcites →https://doi.org/10.1016/s0022-5193(05)80196-1openalex-snapshot
A coupled oscillator feedback system as a model for the photoperiodic clock in insects and mites. II. Simulations of photoperiodic responses
inferredcites →https://doi.org/10.1016/s0022-5193(87)80030-9openalex-snapshot
A damped circadian oscillator model of an insect photoperiodic clock. I. Description of the model based on a feedback control system
inferredcites →https://doi.org/10.1016/s0022-5193(87)80031-0openalex-snapshot
A damped circadian oscillator model of an insect photoperiodic clock
inferredcites →https://doi.org/10.1016/s0022-5193(87)80032-2openalex-snapshot
A damped circadian oscillator model of an insect photoperiodic clock
inferredcites →https://doi.org/10.1016/s0092-8674(00)81637-2openalex-snapshot
CRY, a Drosophila Clock and Light-Regulated Cryptochrome, Is a Major Contributor to Circadian Rhythm Resetting and Photosensitivity
inferredcites →https://doi.org/10.1038/nprot.2006.79openalex-snapshot
Analysis of locomotor activity rhythms in Drosophila
inferredcites →https://doi.org/10.1073/pnas.69.9.2734openalex-snapshot
Circadian Surfaces and the Diversity of Possible Roles of Circadian Organization in Photoperiodic Induction
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/10.1086/335992openalex-snapshot
Studies on the Nature of the Endogenous Rhythm Affecting Photoperiodic Response of Biloxi Soybean
inferredcites →https://doi.org/10.1111/j.1365-2435.2007.01343.xopenalex-snapshot
Genomic approaches for studying biological clocks
inferredcites →https://doi.org/10.1111/j.1365-3032.2012.00837.xopenalex-snapshot
Insect photoperiodism: seeing the light
inferredcites →https://doi.org/10.1111/j.1438-8677.1937.tb01941.xopenalex-snapshot
51. Erwin Bünning: Die endonome Tagesrhythmik als Grundlage der photoperiodischen Reaktion
inferredcites →https://doi.org/10.1111/j.1570-7458.2005.00345.xopenalex-snapshot
Photoperiodic response of diapause induction in the pine caterpillar, Dendrolimus punctatus
inferredcites →https://doi.org/10.1111/j.1751-1097.1969.tb07286.xopenalex-snapshot
COMMON FEATURES OF PHOTOPERIODISM IN PLANTS AND ANIMALS*
inferredcites →https://doi.org/10.1146/annurev-ento-112408-085301openalex-snapshot
Beyond Drosophila: RNAi In Vivo and Functional Genomics in Insects
inferredcites →https://doi.org/10.1177/0748730410365656openalex-snapshot
What Season Is It Anyway? Circadian Tracking vs. Photoperiodic Anticipation in Insects
inferredcites →https://doi.org/10.1177/074873048700200102openalex-snapshot
Diapause Induction and Termination: North-South Strain Differences in Ostrinia nubilalis
inferredcites →https://doi.org/10.1177/074873049901400202openalex-snapshot
Photoperiodic Time Measurement in Insects: A Review of Clock Models
inferredcites →https://doi.org/10.5281/zenodo.10754122openalex-snapshot
Malt as a culture medium for Drosophila species.
inferredcites →https://doi.org/10.5281/zenodo.10763236openalex-snapshot
The Circadian Oscillation in Drosophila pseudoobscura pupae: A Model for the Photoperiodic Clock.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s10682-015-9755-xopenalex-snapshot
Latitudinal differences in diapause related photoperiodic responses of European Colorado potato beetles (Leptinotarsa decemlineata)
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/10.1080/19336934.2021.2016327openalex-snapshot
Adaptation and ecological speciation in seasonally varying environments at high latitudes: Drosophila virilis group
inferred← citeshttps://doi.org/10.1111/eea.12443openalex-snapshot
The influence of temperature and photoperiod on the reproductive diapause and cold tolerance of spotted‐wing drosophila, D rosophila suzukii
inferred← citeshttps://doi.org/10.1111/phen.12165openalex-snapshot
Drosophila ezoana uses an hour‐glass or highly damped circadian clock for measuring night length and inducing diapause
inferred← citeshttps://doi.org/10.1146/annurev-ento-011019-025116openalex-snapshot
Dormancy, Diapause, and the Role of the Circadian System in Insect Photoperiodism
inferred← citeshttps://doi.org/10.1177/0748730421997265openalex-snapshot
Nanda-Hamner Curves Show Huge Latitudinal Variation but No Circadian Components in Drosophila Montana Photoperiodism
inferred← citeshttps://doi.org/10.1177/07487304261461316openalex-snapshot
Latitudinal Clines in Diapause Onset and Circadian Clock Characteristics in Drosophila littoralis and Drosophila montana
inferred← citeshttps://doi.org/10.1242/jeb.113233openalex-snapshot
Functional circadian clock genes are essential for the overwintering diapause of the Northern house mosquito,Culex pipiens
inferred← citeshttps://doi.org/10.1242/jeb.205831openalex-snapshot
Selection for reproduction under short photoperiods changes diapause-associated traits and induces widespread genomic divergence
inferred← citeshttps://doi.org/10.1371/journal.pone.0138758openalex-snapshot
Drosophila americana Diapausing Females Show Features Typical of Young Flies
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