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What Season Is It Anyway? Circadian Tracking vs. Photoperiodic Anticipation in Insects
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471459186.ch3openalex-snapshot
Drosophila Melanogaster : A Model System for Molecular Chronobiology
inferredcites →https://doi.org/10.1007/978-1-4615-6552-9_7openalex-snapshot
Circadian Systems: Entrainment
inferredcites →https://doi.org/10.1007/bf00612503openalex-snapshot
Geographical variation in circadian eclosion rhythm and photoperiodic adult diapause inDrosophila littoralis
inferredcites →https://doi.org/10.1007/s00359-008-0334-2openalex-snapshot
Extrinsic light:dark cycles, rather than endogenous circadian cycles, affect the photoperiodic counter in the pitcher-plant mosquito, Wyeomyia smithii
inferredcites →https://doi.org/10.1007/s00359-009-0416-9openalex-snapshot
Evolution of photoperiodic time measurement is independent of the circadian clock in the pitcher-plant mosquito, Wyeomyia smithii
inferredcites →https://doi.org/10.1007/s12035-008-8035-yopenalex-snapshot
A Plastic Clock: How Circadian Rhythms Respond to Environmental Cues in Drosophila
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(73)90237-0openalex-snapshot
Photoperiodic time measurement in the aphid Megoura viciae
inferredcites →https://doi.org/10.1016/j.cub.2008.07.040openalex-snapshot
New Insights into Ancient Seasonal Life Timers
inferredcites →https://doi.org/10.1016/j.jinsphys.2005.01.005openalex-snapshot
How similar are daily and seasonal biological clocks?
inferredcites →https://doi.org/10.1016/j.jinsphys.2005.03.011openalex-snapshot
Geographic and developmental variation in expression of the circadian rhythm gene, timeless, in the pitcher-plant mosquito, Wyeomyia smithii
inferredcites →https://doi.org/10.1016/j.jinsphys.2006.09.003openalex-snapshot
A nondiapausing variant of the flesh fly, Sarcophaga bullata, that shows arrhythmic adult eclosion and elevated expression of two circadian clock genes, period and timeless
inferredcites →https://doi.org/10.1016/j.jinsphys.2009.01.005openalex-snapshot
Length variation in a specific region of the period gene correlates with differences in pupal diapause incidence in the flesh fly, Sarcophaga bullata
inferredcites →https://doi.org/10.1016/j.tig.2007.12.003openalex-snapshot
Clines in clock genes: fine-tuning circadian rhythms to the environment
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(02)00108-7openalex-snapshot
Short-day and long-day expression patterns of genes involved in the flesh fly clock mechanism: period, timeless, cycle and cryptochrome
inferredcites →https://doi.org/10.1016/s0065-2660(03)48000-0openalex-snapshot
Genetics and molecular biology of rhythms in Drosophila and other insects
inferredcites →https://doi.org/10.1016/s0092-8674(01)00545-1openalex-snapshot
Microarray Analysis and Organization of Circadian Gene Expression in Drosophila
inferredcites →https://doi.org/10.1016/s0896-6273(00)80834-xopenalex-snapshot
How a Circadian Clock Adapts to Seasonal Decreases in Temperature and Day Length
inferredcites →https://doi.org/10.1016/s0896-6273(01)00515-3openalex-snapshot
Circadian Regulation of Gene Expression Systems in the Drosophila Head
inferredcites →https://doi.org/10.1016/s0959-4388(98)80096-2openalex-snapshot
Functional and evolutionary implications of natural variation in clock genes
inferredcites →https://doi.org/10.1017/cbo9780511525834openalex-snapshot
The Ecology of Insect Overwintering
inferredcites →https://doi.org/10.1038/380129a0openalex-snapshot
A light-entrainment mechanism for the Drosophila circadian clock
inferredcites →https://doi.org/10.1073/pnas.86.10.3748openalex-snapshot
Induction of diapause in Drosophila melanogaster: photoperiodic regulation and the impact of arrhythmic clock mutations on time measurement.
inferredcites →https://doi.org/10.1081/cbi-120026099openalex-snapshot
Adaptive Significance of Circadian 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/10.1086/374344openalex-snapshot
Circadian Rhythmicity and Photoperiodism in the Pitcher‐Plant Mosquito: Adaptive Response to the Photic Environment or Correlated Response to the Seasonal Environment?
inferredcites →https://doi.org/10.1086/501032openalex-snapshot
Circadian Rhythmicity and Photoperiodism in the Pitcher‐Plant Mosquito: Can the Seasonal Timer Evolve Independently of the Circadian Clock?
inferredcites →https://doi.org/10.1093/icb/4.4.443openalex-snapshot
BIOLOGY, MOLECULAR AND ORGANISMIC
inferredcites →https://doi.org/10.1093/nar/25.3.455openalex-snapshot
Conceptual translation of timeless reveals alternative initiating methionines in Drosophila
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.1960.025.01.028openalex-snapshot
Some Aspects of Animal Photoperiodism
inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb00458.xopenalex-snapshot
ADAPTATION TO TEMPERATE CLIMATES
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.1365-294x.2007.03509.xopenalex-snapshot
Genetic response to rapid climate change: it's seasonal timing that matters
inferredcites →https://doi.org/10.1111/j.1365-3032.1981.tb00264.xopenalex-snapshot
Insect photoperiodism — the clock and the counter: a review
inferredcites →https://doi.org/10.1111/j.1365-3032.2009.00699.xopenalex-snapshot
Circadian rhythms and the evolution of photoperiodic timing in insects
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.1479-8425.2006.00226.xopenalex-snapshot
Genome-wide screenings for circadian clock genes in Drosophila
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00324.xopenalex-snapshot
CONCORDANCE OF THE CIRCADIAN CLOCK WITH THE ENVIRONMENT IS NECESSARY TO MAXIMIZE FITNESS IN NATURAL POPULATIONS
inferredcites →https://doi.org/10.1126/science.1085935openalex-snapshot
Circadian Clocks in Daily and Seasonal Control of Development
inferredcites →https://doi.org/10.1126/science.1138412openalex-snapshot
Natural Selection Favors a Newly Derived timeless Allele in Drosophila melanogaster
inferredcites →https://doi.org/10.1126/science.1138426openalex-snapshot
A Molecular Basis for Natural Selection at the timeless Locus in Drosophila melanogaster
inferredcites →https://doi.org/10.1126/science.271.5256.1736openalex-snapshot
Light-Induced Degradation of TIMELESS and Entrainment of the Drosophila Circadian Clock
inferredcites →https://doi.org/10.1126/science.278.5346.2117openalex-snapshot
Natural Variation in a Drosophila Clock Gene and Temperature Compensation
inferredcites →https://doi.org/10.1126/science.285.5427.553openalex-snapshot
Light-Dependent Sequestration of TIMELESS by CRYPTOCHROME
inferredcites →https://doi.org/10.1146/annurev.ecolsys.37.091305.110115openalex-snapshot
Evolution of Animal Photoperiodism
inferredcites →https://doi.org/10.1175/1520-0493(1920)48<415b:eotrlo>2.0.co;2openalex-snapshot
EFFECT OF THE RELATIVE LENGTH OF DAY AND NIGHT AND OTHER FACTORS OF THE ENVIRONMENT ON GROWTH AND REPRODUCTION IN PLANTS1
inferredcites →https://doi.org/10.1177/074873001129002088openalex-snapshot
Insect Photoperiodism and Circadian Clocks: Models and Mechanisms
inferredcites →https://doi.org/10.1177/0748730405283418openalex-snapshot
Independence of Genetic Geographical Variation between Photoperiodic Diapause, Circadian Eclosion Rhythm, and Thr-Gly Repeat Region of the Period Gene in Drosophila littoralis
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/10.1177/074873048600100202openalex-snapshot
Genetic Correlation between Circadian Eclosion Rhythm and Photoperiodic Diapause in Drosophila littoralis
inferredcites →https://doi.org/10.1177/074873049000500404openalex-snapshot
The Circadian Basis of Ovarian Diapause Regulation in Drosophila melanogaster: Is the period Gene Causally Involved in Photoperiodic Time Measurement?
inferredcites →https://doi.org/10.1177/074873049100600402openalex-snapshot
The Amplitude of Circadian Oscillations: Temperature Dependence, Latitudinal Clines, and the Photoperiodic Time Measurement
inferredcites →https://doi.org/10.1177/074873049901400202openalex-snapshot
Photoperiodic Time Measurement in Insects: A Review of Clock Models
inferredcites →https://doi.org/10.1371/journal.pone.0009574openalex-snapshot
Microarrays Reveal Early Transcriptional Events during the Termination of Larval Diapause in Natural Populations of the Mosquito, Wyeomyia smithii
inferredcites →https://doi.org/10.1534/genetics.106.068726openalex-snapshot
Quantitative Trait Loci Associated with Photoperiodic Response and Stage of Diapause in the Pitcher-Plant Mosquito, Wyeomyia smithii
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.5281/zenodo.10741286openalex-snapshot
Photoperiodism and seasonal development of insects.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/arch.21366openalex-snapshot
The expression patterns of the clock genes period and timeless are affected by photoperiod in the Mediterranean corn stalk borer, Sesamia nonagrioides
inferred← citeshttps://doi.org/10.1002/bies.201200012openalex-snapshot
Circadian clocks in changing weather and seasons: Lessons from the picoalga Ostreococcus tauri
inferred← citeshttps://doi.org/10.1002/ece3.11713openalex-snapshot
Testing for variation in photoperiodic plasticity in a butterfly: Inconsistent effects of circadian genes between geographic scales
inferred← citeshttps://doi.org/10.1007/978-3-031-36316-0_26openalex-snapshot
The Necessity of Natural Darkness for Humans and Biodiversity
inferred← citeshttps://doi.org/10.1007/978-3-319-08945-4_2openalex-snapshot
Oxidative Stress and Its Role in the Synchronization of Circadian Rhythms in Crustaceans: An Ecological Perspective
inferred← citeshttps://doi.org/10.1007/s00359-023-01643-9openalex-snapshot
Clock-talk: have we forgotten about geographic variation?
inferred← citeshttps://doi.org/10.1007/s00359-023-01646-6openalex-snapshot
Drosophila ezoana uses morning and evening oscillators to adjust its rhythmic activity to different daylengths but only the morning oscillator to measure night length for photoperiodic responses
inferred← citeshttps://doi.org/10.1007/s00359-023-01647-5openalex-snapshot
Impact of photoperiod and functional clock on male diapause in cryptochrome and pdf mutants in the linden bug Pyrrhocoris apterus
inferred← citeshttps://doi.org/10.1007/s10336-011-0708-zopenalex-snapshot
Circadian control of nocturnal songbird migration
inferred← citeshttps://doi.org/10.1007/s10340-016-0741-zopenalex-snapshot
Accelerating research on Spotted Wing Drosophila management using genomic technologies
inferred← citeshttps://doi.org/10.1007/s42690-022-00920-5openalex-snapshot
Seasonality but not photoperiodism affects pesticide toxicity to the two-spotted spider mite, Tetranychus urticae Koch (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.1016/b978-0-08-088504-9.00242-7openalex-snapshot
Circadian Clocks/Photoperiodism and Crop Quality
inferred← citeshttps://doi.org/10.1016/b978-0-12-401667-5.00004-3openalex-snapshot
Living and Adapting to Its Own Habitat
inferred← citeshttps://doi.org/10.1016/b978-0-12-415819-1.00005-2openalex-snapshot
Behavioral Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-417156-5.00013-7openalex-snapshot
Modeling Bark Beetle Responses to Climate Change
inferred← citeshttps://doi.org/10.1016/b978-0-12-820359-0.00004-9openalex-snapshot
Behavioral systems
inferred← citeshttps://doi.org/10.1016/b978-0-444-59427-3.00027-7openalex-snapshot
Two clocks in the brain
inferred← citeshttps://doi.org/10.1016/b978-0-444-64046-8.00260-3openalex-snapshot
Circadian Clocks/Photoperiodism and Crop Quality
inferred← citeshttps://doi.org/10.1016/bs.adgen.2017.09.002openalex-snapshot
Natural Variation and Genetics of Photoperiodism in Wyeomyia smithii
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.05.142openalex-snapshot
Photoperiodic response requires mammalian-type cryptochrome in the bean bug Riptortus pedestris
inferred← citeshttps://doi.org/10.1016/j.cbpb.2017.03.003openalex-snapshot
The expression of the clock gene cycle has rhythmic pattern and is affected by photoperiod in the moth Sesamia nonagrioides
inferred← citeshttps://doi.org/10.1016/j.cbpb.2023.110849openalex-snapshot
Circadian clock genes and photoperiodic diapause in the moth Sesamia nonagrioides
inferred← citeshttps://doi.org/10.1016/j.cois.2014.12.002openalex-snapshot
Photoperiodic time measurement in insects
inferred← citeshttps://doi.org/10.1016/j.cub.2019.08.053openalex-snapshot
Genomic Basis of Circannual Rhythm in the European Corn Borer Moth
inferred← citeshttps://doi.org/10.1016/j.cub.2019.09.061openalex-snapshot
Chronobiology: The Circadian Clock under Extreme Photoperiods
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.07.016openalex-snapshot
A metabolic daylength measurement system mediates winter photoperiodism in plants
inferred← citeshttps://doi.org/10.1016/j.ecolind.2024.111566openalex-snapshot
Listening to tropical forest soils
inferred← citeshttps://doi.org/10.1016/j.febslet.2011.02.026openalex-snapshot
The hormonal and circadian basis for insect photoperiodic timing
inferred← citeshttps://doi.org/10.1016/j.ibmb.2017.02.006openalex-snapshot
Characterisation, analysis of expression and localisation of circadian clock genes from the perspective of photoperiodism in the aphid Acyrthosiphon pisum
inferred← citeshttps://doi.org/10.1016/j.ibmb.2025.104298openalex-snapshot
Evolution of circadian clock and light-input pathway genes in Hemiptera
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2010.10.006openalex-snapshot
Insect photoperiodic calendar and circadian clock: Independence, cooperation, or unity?
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2011.01.013openalex-snapshot
Deciphering time measurement: The role of circadian ‘clock’ genes and formal experimentation in insect photoperiodism
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2012.09.007openalex-snapshot
Photoperiodic regulation of life-history traits before and after eclosion: Egg-to-adult development time, juvenile body mass and reproductive diapause in Drosophila montana
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2012.11.003openalex-snapshot
Insect photoperiodism: Measuring the night
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2013.04.007openalex-snapshot
Involvement of circadian oscillation(s) in the photoperiodic time measurement and the induction of reproductive diapause in a northern Drosophila species
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2013.06.004openalex-snapshot
Endocrine regulation of non-circadian behavior of circadian genes in insect gut
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2014.08.004openalex-snapshot
Embryonic diapause in the Australian plague locust relative to parental experience of cumulative photophase decline
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2017.11.009openalex-snapshot
Characterisation, analysis of expression and localisation of the opsin gene repertoire from the perspective of photoperiodism in the aphid Acyrthosiphon pisum
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2019.103901openalex-snapshot
Gene expression changes in response to field-to-lab transition in the Argentine ant, Linepithema humile
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2021.104232openalex-snapshot
Increased size and energy reserves in diapausing eggs of temperate Aedes aegypti populations
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2023.104556openalex-snapshot
Clinal variation in the temperature and photoperiodic control of reproductive diapause in Drosophila montana females
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2026.104957openalex-snapshot
Molecular characterization and seasonal expression profiling of circadian clock genes in relation to obligatory diapause in the Sunn Pest, Eurygaster integriceps (Hemiptera: Scutelleridae)
inferred← citeshttps://doi.org/10.1016/j.limno.2018.11.002openalex-snapshot
Benthic life in karst spring—The life cycle and secondary production of benthic macroinvertebrates under the effects of constant water temperature
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2012.07.003openalex-snapshot
Neuromodulatory role of melatonin in retinal information processing
inferred← citeshttps://doi.org/10.1016/j.zool.2020.125856openalex-snapshot
Geographic clines in Daphnia magna’s circadian clock gene expression: Local adaptation to photoperiod
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/10.1017/s0140525x18002157openalex-snapshot
Thinking in and about time: A dual systems perspective on temporal cognition
inferred← citeshttps://doi.org/10.1038/hdy.2011.108openalex-snapshot
Genetic correlations and the evolution of photoperiodic time measurement within a local population of the pitcher-plant mosquito, Wyeomyia smithii
inferred← citeshttps://doi.org/10.1038/s41597-020-00751-4openalex-snapshot
Daily transcriptomes of the copepod Calanus finmarchicus during the summer solstice at high Arctic latitudes
inferred← citeshttps://doi.org/10.1038/s41598-020-77065-3openalex-snapshot
The expression of circadian clock genes in Daphnia magna diapause
inferred← citeshttps://doi.org/10.1038/srep45412openalex-snapshot
Migration phenology and breeding success are predicted by methylation of a photoperiodic gene in the barn swallow
inferred← citeshttps://doi.org/10.1073/pnas.1217060110openalex-snapshot
Autonomous regulation of the insect gut by circadian genes acting downstream of juvenile hormone signaling
inferred← citeshttps://doi.org/10.1080/03014223.2018.1549084openalex-snapshot
Pathways of ocular entrainment in Marpissa marina (Araneae, Salticidae)
inferred← citeshttps://doi.org/10.1080/03949370.2025.2564807openalex-snapshot
Evaluating the impacts of a total solar eclipse on Midwest prairie soundscape
inferred← citeshttps://doi.org/10.1080/07420528.2019.1649275openalex-snapshot
Diurnal variation in sperm DNA fragmentation: analysis of 11,382 semen samples from two populations andin vivoanimal experiments
inferred← citeshttps://doi.org/10.1080/07420528.2023.2195942openalex-snapshot
Photoperiodic adaptation of aanat and clock gene expression in seasonal populations of Daphnia pulex
inferred← citeshttps://doi.org/10.1086/664709openalex-snapshot
Rapid Adaptive Evolution of Photoperiodic Response during Invasion and Range Expansion across a Climatic Gradient
inferred← citeshttps://doi.org/10.1086/708678openalex-snapshot
Phenotypic Variation in Growth and Gene Expression Under Different Photoperiods in Allopatric Populations of the Copepod Tigriopus californicus
inferred← citeshttps://doi.org/10.1093/ee/nvx165openalex-snapshot
Photophase Duration Affects Immature Black Soldier Fly (Diptera: Stratiomyidae) Development
inferred← citeshttps://doi.org/10.1093/jisesa/iew013openalex-snapshot
Pea Aphids (Hemiptera: Aphididae) Have Diurnal Rhythms When Raised Independently of a Host Plant
inferred← citeshttps://doi.org/10.1093/pnasnexus/pgac046openalex-snapshot
Artificial light at night: an underappreciated effect on phenology of deciduous woody plants
inferred← citeshttps://doi.org/10.1098/rsbl.2012.0216openalex-snapshot
Street lighting changes the composition of invertebrate communities
inferred← citeshttps://doi.org/10.1098/rspb.2012.1917openalex-snapshot
Footprints in time: comparative quantitative trait loci mapping of the pitcher-plant mosquito,Wyeomyia smithii
inferred← citeshttps://doi.org/10.1098/rspb.2018.0367openalex-snapshot
Artificial light at night decreases metamorphic duration and juvenile growth in a widespread amphibian
inferred← citeshttps://doi.org/10.1098/rstb.2016.0257openalex-snapshot
Keeping time without a spine: what can the insect clock teach us about seasonal adaptation?
inferred← citeshttps://doi.org/10.1101/2020.11.13.381426openalex-snapshot
A Metabolic Coincidence Mechanism Controls Winter Photoperiodism in Plants
inferred← citeshttps://doi.org/10.1101/2021.09.29.462474openalex-snapshot
Roles of PKCdelta in Photoperiod and Circadian Regulations in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1101/2022.03.09.483610openalex-snapshot
Seasonality but not photoperiodism affects susceptibility of the two-spotted spider mite, Tetranychus urticae Koch (Acari: Tetranychidae) to pesticides
inferred← citeshttps://doi.org/10.1111/imb.12050openalex-snapshot
Identification, characterization and analysis of expression of genes encoding arylalkylamine N ‐acetyltransferases in the pea aphid A cyrthosiphon pisum
inferred← citeshttps://doi.org/10.1111/imb.12747openalex-snapshot
Mapping and quantification of cryptochrome expression in the brain of the pea aphid Acyrthosiphon pisum
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2011.05133.xopenalex-snapshot
Testing for causality in covarying traits: genes and latitude in a molecular world
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2012.08666.xopenalex-snapshot
Robust and flexible response of the Ostreococcus tauri circadian clock to light/dark cycles of varying photoperiod
inferred← citeshttps://doi.org/10.1111/jfb.12024openalex-snapshot
Geography of the circadian gene clock and photoperiodic response in western North American populations of the three‐spined sticklebackGasterosteus aculeatus
inferred← citeshttps://doi.org/10.1111/mec.13202openalex-snapshot
Localization of quantitative trait loci for diapause and other photoperiodically regulated life history traits important in adaptation to seasonally varying environments
inferred← citeshttps://doi.org/10.1111/mec.14501openalex-snapshot
Gene expression profiling across ontogenetic stages in the wood white (Leptidea sinapis) reveals pathways linked to butterfly diapause regulation
inferred← citeshttps://doi.org/10.1111/mec.15001openalex-snapshot
The genetic architecture underlying diapause termination in a planktonic crustacean
inferred← citeshttps://doi.org/10.1111/mec.16331openalex-snapshot
Local adaptation of life cycles in a butterfly is associated with variation in several circadian clock genes
inferred← citeshttps://doi.org/10.1111/phen.12159openalex-snapshot
Diapause induction as an interplay between seasonal token stimuli, and modifying and directly limiting factors: hibernation in Chymomyza costata
inferred← citeshttps://doi.org/10.1177/0748730416671213openalex-snapshot
Unexpected Geographic Variability of the Free Running Period in the Linden Bug Pyrrhocoris apterus
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/10.1186/1741-7007-8-115openalex-snapshot
Circadian clock genes, ovarian development and diapause
inferred← citeshttps://doi.org/10.1186/s40851-014-0003-yopenalex-snapshot
Common features in diverse insect clocks
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/10.12933/therya-24-5029openalex-snapshot
Activity patterns of the white-tailed deer (Odocoileus virginianus) in a neotropical dry forest: changes according to age, sex, and climatic season
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004603openalex-snapshot
Role for Circadian Clock Genes in Seasonal Timing: Testing the Bünning Hypothesis
inferred← citeshttps://doi.org/10.1371/journal.pntd.0003724openalex-snapshot
Global Transcriptional Dynamics of Diapause Induction in Non-Blood-Fed and Blood-Fed Aedes albopictus
inferred← citeshttps://doi.org/10.1371/journal.pone.0027493openalex-snapshot
Association between Circadian Clock Genes and Diapause Incidence in Drosophila triauraria
inferred← citeshttps://doi.org/10.1371/journal.pone.0069439openalex-snapshot
Gene Expression-Based Biomarkers for Anopheles gambiae Age Grading
inferred← citeshttps://doi.org/10.15226/2576-4934/2/1/00111openalex-snapshot
The Cryptochrome1 (cry1) Gene has Oscillating Expression Under Short and Long Photoperiods inSesamia nonagrioides
inferred← citeshttps://doi.org/10.1665/034.022.0108openalex-snapshot
Daily Temperature Cycle Induces Daily Hatching Rhythm in Eastern Lubber Grasshoppers,Romalea microptera
inferred← citeshttps://doi.org/10.1890/13-1996.1openalex-snapshot
Transgenerational phenotypic plasticity links breeding phenology with offspring life‐history
inferred← citeshttps://doi.org/10.2147/rrb.s126279openalex-snapshot
Photoperiodic control of diapause induction in the zygaenid moth Thyrassia penangae – involving day-length measurement
inferred← citeshttps://doi.org/10.2741/4129openalex-snapshot
ROS signaling pathways and biological rhythms: perspectives in crustaceans
inferred← citeshttps://doi.org/10.3109/07420528.2014.880451openalex-snapshot
Phylogeny and oscillating expression of period and cryptochrome in short and long photoperiods suggest a conserved function in Nasonia vitripennis
inferred← citeshttps://doi.org/10.3389/fnbeh.2022.778264openalex-snapshot
Maternally Instigated Diapause in Aedes albopictus: Coordinating Experience and Internal State for Survival in Variable Environments
inferred← citeshttps://doi.org/10.3389/fphys.2015.00400openalex-snapshot
“The Environment is Everything That Isn't Me”: Molecular Mechanisms and Evolutionary Dynamics of Insect Clocks in Variable Surroundings
inferred← citeshttps://doi.org/10.3390/antiox14101151openalex-snapshot
Light-Induced Transcription in Zebrafish Targets Mitochondrial Function and Heme Metabolism
inferred← citeshttps://doi.org/10.3390/genes14020292openalex-snapshot
Seasonal Adaptation: Geographic Photoperiod–Temperature Patterns Explain Genetic Variation in the Common Vole Tsh Receptor
inferred← citeshttps://doi.org/10.3390/ijms23094935openalex-snapshot
Photoperiod-Dependent Expression of MicroRNA in Drosophila
inferred← citeshttps://doi.org/10.3390/insects16020182openalex-snapshot
Adult Diel Locomotor Behaviour in the Agricultural Pest Plutella xylostella Reflects Temperature-Driven and Light-Repressed Regulation Rather than Coupling to Circadian Clock Gene Rhythms
inferred← citeshttps://doi.org/10.4039/tce.2019.18openalex-snapshot
Shedding new light upon circadian emergence rhythmicity in the mountain pine beetle (Coleoptera: Curculionidae: Scolytinae)
inferred← citeshttps://doi.org/10.64898/2026.09.11.750828openalex-snapshot
Lunar Reproductive Timing Acts as a Magic Trait and May Recruit Additional Isolating Barriers in Sympatric Marine Midge Populations
inferred← citeshttps://doi.org/10.70675/29bdc427z4ac7z4deaz8c5ez4d03b58f4676openalex-snapshot
Variabilité de la diapause chez les parasitoïdes de pucerons dans le cadre des changements climatiques : implications en lutte biologique
inferred← citeshttps://doi.org/10.70675/c5297ca8z900az4bcdzaf6bz970c132aee0fopenalex-snapshot
Taking light pollution effects on biodiversity into account in conservation measures : challenges and prospects. Case study of European bat species
inferred← citeshttps://doi.org/10.7717/peerj.11786openalex-snapshot
Seasonal variation in the diel activity of a dung beetle assemblage
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