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An experimental and theoretical analysis of photoperiodic induction in the flesh-Fly,Sarcophaga argyrostoma

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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/bf00606467openalex-snapshot
Insect photoperiodism: An hourglass measures photoperiodic time inOstrinia nubilalis
inferredcites →https://doi.org/10.1007/bf00617123openalex-snapshot
Photoperiodic determination of insect development and diapause
inferredcites →https://doi.org/10.1007/bf00645355openalex-snapshot
?Skeleton? photoperiods and the control of diapause and development in the flesh-fly,Sarcophaga argyrostoma
inferredcites →https://doi.org/10.1007/bf00656785openalex-snapshot
The circadian eclosion rhythm inSarcophaga argyrostoma: Some comparisons with the photoperiodic “clock”
inferredcites →https://doi.org/10.1007/bf00694944openalex-snapshot
Slow dark-adaptation inDrosophila's circadian clock
inferredcites →https://doi.org/10.1007/bf00701477openalex-snapshot
Photoperiodic determination of insect development and diapause
inferredcites →https://doi.org/10.1007/bf00701478openalex-snapshot
Photoperiodic determination of insect development and diapause
inferredcites →https://doi.org/10.1007/bf01379287openalex-snapshot
Photoperiodic determination of insect development and diapause
inferredcites →https://doi.org/10.1016/0022-1910(68)90067-xopenalex-snapshot
Photoperiodic control of diapause in the codling moth
inferredcites →https://doi.org/10.1016/0022-1910(69)90171-1openalex-snapshot
Hour-glass dusk and rhythmic dawn timers control diapause in the codling moth
inferredcites →https://doi.org/10.1016/0022-1910(71)90098-9openalex-snapshot
The temperature-compensated photoperiodic clock ‘programming’ development and pupal diapause in the flesh-fly, Sarcophaga argyrostoma
inferredcites →https://doi.org/10.1016/0022-1910(73)90188-1openalex-snapshot
The photoperiodic clock in the flesh-fly, Sarcophaga argyrostoma
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(74)90125-5openalex-snapshot
Evidence for ‘dawn’ and ‘dusk’ oscillators in the Nasonia photoperiodic clock
inferredcites →https://doi.org/10.1016/0022-5193(70)90075-5openalex-snapshot
Integrated view of resetting a circadian clock
inferredcites →https://doi.org/10.1016/b978-1-4832-2781-8.50008-xopenalex-snapshot
PHOTOPERIODISM IN INSECTS
inferredcites →https://doi.org/10.1038/scientificamerican0276-114openalex-snapshot
The Biological Clock of Insects
inferredcites →https://doi.org/10.1073/pnas.58.4.1762openalex-snapshot
Circadian systems. I. The driving oscillation and its assay in Drosophila pseudoobscura.
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/10.1086/282332openalex-snapshot
Action of the Photoperiod in Controlling Insect Diapause
inferredcites →https://doi.org/10.1101/sqb.1960.025.01.015openalex-snapshot
Circadian Rhythms and the Circadian Organization of Living Systems
inferredcites →https://doi.org/10.1101/sqb.1960.025.01.029openalex-snapshot
Photoperiodism and Circadian Rhythms
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/10.1126/science.1257756openalex-snapshot
Insect Photoperiodism: The "T Experiment" as Evidence for an Hourglass Mechanism
inferredcites →https://doi.org/10.1126/science.142.3597.1294openalex-snapshot
Diurnal Rhythm and Photoperiodism in Testicular Recrudescence of the House Finch
inferredcites →https://doi.org/10.1126/science.168.3931.601openalex-snapshot
Circadian Clock in Insect Photoperiodism
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/10.1242/jeb.41.1.119openalex-snapshot
The Location of the Photoperiodic Receptors in the Aphid Megoura Viciae Buckton
inferredcites →https://doi.org/10.2307/1539252openalex-snapshot
PHYSIOLOGY OF INSECT DIAPAUSE. XIV. AN ENDOCRINE MECHANISM FOR THE PHOTOPERIODIC CONTROL OF PUPAL DIAPAUSE IN THE OAK SILKWORM, ANTHERAEA PERNYI

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Weak and Strong Resetting of the Onion Fly Circadian Clock in Response to 1 °C and 4 °C Changes
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The Effect of Light on the Human Circadian Pacemaker
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Long‐Night Summation and Programming of Pupal Diapause in the Flesh‐Fly, Sarcophaga argyrostoma
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Daily and Seasonal Rhythms
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Daily and Seasonal Rhythms
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Photoperiodism in Insects and Other Animals
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The Physiology of Pupal Diapause in Flesh Flies
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Insect Photoperiodism
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Circadian Frequency and Its Variability
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The photoperiodic clock and ?counter? in Sarcophaga argyrostoma: experimental evidence consistent with ?external coincidence? in insect photoperiodism
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Dynamic response of a circadian pacemaker
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Photoperiodic time measurement in spider mites
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Photoperiodic time measurement in spider mites
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Photoperiodic time measurement inSarcophaga argyrostoma: An attempt to use daily temperature cycles to distinguish external from internal coincidence
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External coincidence and the photoinducible phase in theSarcophaga photoperiodic clock
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Geographical variation in circadian eclosion rhythm and photoperiodic adult diapause inDrosophila littoralis
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The effects of ultra-short photoperiods on the seasonal clock inSarcophaga argyrostoma
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Phase-resetting a mosquito circadian oscillator
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Photoperiodic induction of pupal diapause in the flesh fly,Sarcophaga crassipalpis: embryonic sensitivity
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Circadian oscillators, cell cycles, and singularities: light perturbations of the free-running rhythm of cell division inEuglena
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Internal and external coincidence and the apparent diversity of photoperiodic clocks in the insects
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Different oscillators control the circadian rhythm of eclosion and activity inDrosophila
inferred← citeshttps://doi.org/10.1007/bf01958896openalex-snapshot
Evidence for the neurohormonal basis of commitment to pupal diapause in larvae ofSarcophaga argyrostoma
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A phase response curve for circannual rhythm in the varied carpet beetle Anthrenus verbasci
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Phase resetting and phase singularity of an insect circannual oscillator
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Photoperiodic time measurement in the spider mite Tetranychus urticae: A novel concept
inferred← citeshttps://doi.org/10.1016/0022-1910(82)90041-5openalex-snapshot
Photoperiodic induction of pupal diapause in Sarcophaga argyrostoma: Temperature effects on circadian resonance
inferred← citeshttps://doi.org/10.1016/0022-1910(82)90122-6openalex-snapshot
External coincidence and photoperiodic time measurement in the spider mite Tetranychus urticae
inferred← citeshttps://doi.org/10.1016/0022-1910(85)90085-xopenalex-snapshot
An “hourglass-like” feature in the photoperiodic time measurement in Diatraea grandiosella (Pyralidae)
inferred← citeshttps://doi.org/10.1016/0022-1910(86)90089-2openalex-snapshot
A “dusk” oscillator affects photoperiodic induction of diapause in the spider mit, Tetranychus urticae
inferred← citeshttps://doi.org/10.1016/0022-1910(86)90122-8openalex-snapshot
Similarities between the photoperiodic clocks of Megoura and Tetranychus: Experiments with spider mites
inferred← citeshttps://doi.org/10.1016/0022-1910(87)90031-xopenalex-snapshot
An instantly damping oscillator model for photoperiodic time measurement in the aphid Aphis fabae
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Weak circadian eclosion rhythmicity in Chymomyza costata (Diptera: Drosophilidae), and its independence of diapause type
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Light-pulse phase response curves for the locomotor activity rhythm in Period mutants of Drosophila melanogaster
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The circadian eclosion rhythm in Sarcophaga argyrostoma: A limit cycle representation of the pacemaker
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A ‘simple clock’ approach of circadian rhythms: An easy way to predict the clock's singularity
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Unity and diversity in the insect photoperiodic mechanism*
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Many Circadian Oscillators Regulate Developmental and Behavioural Events in the Flesh-Fly,Sarcophaga Argyrostoma
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Commentary on Nicholas Mrosovsky's Letter
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Photoperiodic time measurement and seasonal adaptation of the southwestern corn borer, Diatraea grandiosella Dyar (Lepidoptera : Pyralidae)
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Rapid phase resetting of Aedes aegypti circadian rhythms by transient alterations in light exposure
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