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Effects of photoperiod, temperature, food and relative humidity on the induction of diapause in the predatory miteAmblyseius potentillae

https://doi.org/10.1007/bf01194087

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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/bf00612634openalex-snapshot

Existence of a light-sensitive phase in the photoperiodic termination of diapause inPieris brassicae L. (Insecta:Lepidoptera) and comparison with diapause induction

inferredcites →https://doi.org/10.1007/bf00619114openalex-snapshot

Geographic variation in the circadian system controlling photoperiodism inOstrinia nubilalis

inferredcites →https://doi.org/10.1007/bf01197922openalex-snapshot

Effect of diet on the photoperiodic induction of diapause in three species of predatory mite,Amblyseius potentillae, A. cucumeris andTyphlodromus pyri

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/10.1007/bf01951725openalex-snapshot

Photoperiodic induction of diapause in an insect is vitamin A dependent

inferredcites →https://doi.org/10.1007/bf01960254openalex-snapshot

Occurrence of retinal and 3-hydroxyretinal in a possible photoreceptor of the silkworm brain involved in photoperiodism

inferredcites →https://doi.org/10.1007/bf01980946openalex-snapshot

Genetics of resistance to organophosphorus compounds and its relation to diapause inTetranychus urticae Koch (Acari)

inferredcites →https://doi.org/10.1016/0022-1910(67)90123-0openalex-snapshot

Water intake and the termination of diapause in the European corn borer, Ostrinia nubilalis

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(75)90007-4openalex-snapshot

Diapause in the mite Metaseiulus occidentalis: Stages sensitive to photoperiodic induction

inferredcites →https://doi.org/10.1016/0022-1910(77)90087-7openalex-snapshot

Aspects of the induction of diapause in a laboratory strain of the mite Tetranychus urticae

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(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(85)90049-6openalex-snapshot

The photoperiodic induction of ovarian diapause in the cabbage whitefly, Aleyrodes proletella (Homoptera: Aleyrodidae)

inferredcites →https://doi.org/10.1016/0022-1910(86)90089-2openalex-snapshot

A “dusk” oscillator affects photoperiodic induction of diapause in the spider mit, Tetranychus urticae

inferredcites →https://doi.org/10.1016/0022-1910(86)90122-8openalex-snapshot

Similarities between the photoperiodic clocks of Megoura and Tetranychus: Experiments with spider mites

inferredcites →https://doi.org/10.1016/0022-1910(87)90067-9openalex-snapshot

Photoperiodic time measurement in a Russian strain of the spider mite, Tetranychus urticae

inferredcites →https://doi.org/10.1016/0022-1910(87)90068-0openalex-snapshot

The photoperiodic control of wing development in the black bean aphid, Aphis fabae

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(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/b978-0-120-84380-0.x5001-7openalex-snapshot

Insect Photoperiodism

inferredcites →https://doi.org/10.1016/s0165-8646(24)00617-2openalex-snapshot

Carotenoid functions in photoperiodic induction in the silkworm, Bombyx mori

inferredcites →https://doi.org/10.1038/166874a0openalex-snapshot

Diapause and Photoperiodism in the Fruit Tree Red Spider Mite (Metatetranychus ulmi Koch)

inferredcites →https://doi.org/10.1038/275234a0openalex-snapshot

Evidence for the functional involvement of carotenoids in the photoperiodic reaction of spider mites

inferredcites →https://doi.org/10.1038/302248a0openalex-snapshot

Vitamin A is essential for photoperiodic induction of diapause in an eyeless mite

inferredcites →https://doi.org/10.1080/01647957608683752openalex-snapshot

Geographic races in the predaceous mite,Amblyseius potentillae(Acari: Phytoseiidae)

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/ee/16.1.72openalex-snapshot

Diapause Induction in Amblyseius fallacis (Acari: Phytoseiidae)

inferredcites →https://doi.org/10.1111/j.1365-3032.1980.tb00237.xopenalex-snapshot

Functional involvement of carotenoids in photoperiodic induction of diapause in the spider mite, Tetranychus urticae

inferredcites →https://doi.org/10.1111/j.1365-3032.1989.tb01101.xopenalex-snapshot

Photoperiodic control of adult diapause in the predacious mite, Amblyseius potentillae: repeated diapause induction and termination

inferredcites →https://doi.org/10.1111/j.1439-0418.1982.tb03563.xopenalex-snapshot

Copulation and egg production in Amblyseius potentillae and Typhlodromus pyri (Acari, Phytoseiidae)

inferredcites →https://doi.org/10.1111/j.1570-7458.1983.tb03228.xopenalex-snapshot

THE EFFECT OF DIFFERENT KINDS OF FOOD ON THE INDUCTION OF DIAPAUSE IN THE PREDACIOUS MITE AMBLYSEIUS POTENTILLAE

inferredcites →https://doi.org/10.1111/j.1744-7348.1953.tb02387.xopenalex-snapshot

ENVIRONMENTAL FACTORS CONTROLLING THE EVOCATION AND TERMINATION OF DIAPAUSE IN THE FRUIT TREE RED SPIDER MITE METATETRANYCHUS ULMI KOCH (ACARINA: TETRANYCHIDAE)

inferredcites →https://doi.org/10.1111/j.1744-7348.1953.tb02388.xopenalex-snapshot

THE SIGNIFICANCE OF THE LIGHT AND DARK PHASES IN THE PHOTOPERIODIC CONTROL OF DIAPAUSE IN METATETRANYCHUS ULMI KOCH

inferredcites →https://doi.org/10.1126/science.213.4512.1131openalex-snapshot

Carotenoids Function in Photoperiodic Induction of Diapause in a Predacious Mite

inferredcites →https://doi.org/10.2183/pjab1945.46.541openalex-snapshot

Effect of Non-24-Hour Photo period and Light Interruption of the Dark Phase on Diapause Determination in Papilio xuthus L

inferredcites →https://doi.org/10.4039/ent94163-2openalex-snapshot

Life-History and Behaviour of the Predacious Mite Typhlodromus (T.) caudiglans Schuster (Acarina: Phytoseiidae) in Ontario, with Notes on the Prey of Related Species

What points at this work

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

inferred← citeshttps://doi.org/10.1051/acarologia/20142143zenodo-depositor-declared

Occurrence, population dynamics and winter phenology of spider mites and their phytoseiid predators in a citrus orchard in Syria

inferred← citeshttps://doi.org/10.1007/bf00188113openalex-snapshot

Photoperiodism and thermoperiodism in the predatory mite Amblyseius potentillae are probably based on the same mechanism

inferred← citeshttps://doi.org/10.1007/bf01205351openalex-snapshot

Diapause in phytoseiid mites: a review

inferred← citeshttps://doi.org/10.1007/s00359-013-0872-0openalex-snapshot

Both the anterior and posterior eyes function as photoreceptors for photoperiodic termination of diapause in the two-spotted spider mite

inferred← citeshttps://doi.org/10.1007/s00360-016-1018-9openalex-snapshot

Physiological and molecular mechanisms underlying photoperiodism in the spider mite: comparisons with insects

inferred← citeshttps://doi.org/10.1016/b978-044450407-4/50018-5openalex-snapshot

References A man will turn over half a library to make one book. Samuel Johnson

inferred← citeshttps://doi.org/10.1016/j.baae.2025.03.008openalex-snapshot

Artificial light at night reduces larval survival and constrains female body mass in a capital breeding moth

inferred← citeshttps://doi.org/10.1016/j.jinsphys.2004.01.002openalex-snapshot

Diapause induction and clock mechanism in the cabbage beetle, Colaphellus bowringi (Coleoptera: Chrysomelidae)

inferred← citeshttps://doi.org/10.1111/ens.12059openalex-snapshot

Insect photoperiodism: effects of temperature on the induction of insect diapause and diverse roles for the circadian system in the photoperiodic response

inferred← citeshttps://doi.org/10.1177/074873001129002088openalex-snapshot

Insect Photoperiodism and Circadian Clocks: Models and Mechanisms

inferred← citeshttps://doi.org/10.1177/074873049300800401openalex-snapshot

The Same Photoperiodic Clock May Control Induction and Maintenance of Diapause in the Spider Mite Tetranchus urticae

inferred← citeshttps://doi.org/10.1177/074873049901400202openalex-snapshot

Photoperiodic Time Measurement in Insects: A Review of Clock Models

inferred← citeshttps://doi.org/10.2300/acari.3.59openalex-snapshot

Variations in the Diapause Characteristics of Amblyseius womersleyi Schicha(Acari: Phytoseiidae).

inferred← citeshttps://doi.org/10.3390/biology11091313openalex-snapshot

Transcriptional Dynamics Induced by Diapause Hormone in the Silkworm, Bombyx mori

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