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Unexpected Geographic Variability of the Free Running Period in the Linden Bug Pyrrhocoris apterus

https://doi.org/10.1177/0748730416671213
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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The period gene of Drosophila carries species‐specific behavioral instructions.
inferredcites →https://doi.org/10.1007/bf00612503openalex-snapshot
Geographical variation in circadian eclosion rhythm and photoperiodic adult diapause inDrosophila littoralis
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Spontanperiodik des Menschen bei Ausschluß aller Zeitgeber
inferredcites →https://doi.org/10.1007/s00018-008-7506-7openalex-snapshot
Endocrine-dependent expression of circadian clock genes in insects
inferredcites →https://doi.org/10.1016/0022-1910(83)90067-7openalex-snapshot
A diapause induction-termination asymmetry in the photoperiodic responses of the Linden bug, Pyrrhocoris apterus and an effect of near-critical photoperiods on development
inferredcites →https://doi.org/10.1016/j.cois.2014.12.002openalex-snapshot
Photoperiodic time measurement in insects
inferredcites →https://doi.org/10.1016/j.ibmb.2013.12.003openalex-snapshot
Juvenile hormone signaling during reproduction and development of the linden bug, Pyrrhocoris apterus
inferredcites →https://doi.org/10.1016/j.ibmb.2016.01.003openalex-snapshot
Photoperiod regulates growth of male accessory glands through juvenile hormone signaling in the linden bug, Pyrrhocoris apterus
inferredcites →https://doi.org/10.1016/j.jinsphys.2005.01.009openalex-snapshot
Is period gene causally involved in the photoperiodic regulation of reproductive diapause in the linden bug, Pyrrhocoris apterus?
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.2011.01.013openalex-snapshot
Deciphering time measurement: The role of circadian ‘clock’ genes and formal experimentation in insect photoperiodism
inferredcites →https://doi.org/10.1016/j.jinsphys.2013.06.004openalex-snapshot
Endocrine regulation of non-circadian behavior of circadian genes in insect gut
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(00)81676-1openalex-snapshot
A pdf Neuropeptide Gene Mutation and Ablation of PDF Neurons Each Cause Severe Abnormalities of Behavioral Circadian Rhythms in Drosophila
inferredcites →https://doi.org/10.1038/210329a0openalex-snapshot
‘Paper Factor’ as an Inhibitor of the Embryonic Development of the European Bug, Pyrrhocoris apterus
inferredcites →https://doi.org/10.1038/263521a0openalex-snapshot
Nervous inhibition of corpora allata by photoperiod in Pyrrhocoris apterus
inferredcites →https://doi.org/10.1038/hdy.1993.126openalex-snapshot
North–south differences in circadian eclosion rhythm in European populations of Drosophila subobscura
inferredcites →https://doi.org/10.1038/nature10991openalex-snapshot
Unexpected features of Drosophila circadian behavioural rhythms under natural conditions
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
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Comparative phylogeography and postglacial colonization routes in Europe
inferredcites →https://doi.org/10.1073/pnas.1217060110openalex-snapshot
Autonomous regulation of the insect gut by circadian genes acting downstream of juvenile hormone signaling
inferredcites →https://doi.org/10.1073/pnas.1506093112openalex-snapshot
Drosophila circadian rhythms in seminatural environments: Summer afternoon component is not an artifact and requires TrpA1 channels
inferredcites →https://doi.org/10.1093/genetics/149.1.165openalex-snapshot
Molecular and Behavioral Analysis of Four period Mutants in Drosophila melanogaster Encompassing Extreme Short, Novel Long, and Unorthodox Arrhythmic Types
inferredcites →https://doi.org/10.1093/jmedent/31.1.49openalex-snapshot
Variability in Circadian Activity Patterns within the Culex pipiens Complex (Diptera: Culicidae)
inferredcites →https://doi.org/10.1098/rspb.1992.0128openalex-snapshot
A latitudinal cline in aDrosophilaclock gene
inferredcites →https://doi.org/10.1098/rspb.2013.0433openalex-snapshot
Latitudinal clines: an evolutionary view on biological rhythms,
inferredcites →https://doi.org/10.1098/rstb.2010.0409openalex-snapshot
Evolution of time-keeping mechanisms: early emergence and adaptation to photoperiod
inferredcites →https://doi.org/10.1111/j.1365-3032.1987.tb00728.xopenalex-snapshot
Naturally occurring arrhythmicity in eclosion and activity in Lucilia cuprina: its genetic basis
inferredcites →https://doi.org/10.1111/j.1601-5223.1994.00081.xopenalex-snapshot
Selection for Non-Diapause in the Heteropteran Pyrrhocoris Apterus
inferredcites →https://doi.org/10.1126/science.1082971openalex-snapshot
Enhanced Fitness Conferred by Naturally Occurring Variation in the 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/10.1128/mcb.19.6.4343openalex-snapshot
timrit Lengthens Circadian Period in a Temperature-Dependent Manner through Suppression of PERIOD Protein Cycling and Nuclear Localization
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/10.1177/0748730407303624openalex-snapshot
Photoperiodic and Food Signals Control Expression Pattern of the Clock Gene, Period, in the Linden Bug, Pyrrhocoris apterus
inferredcites →https://doi.org/10.1177/0748730410365656openalex-snapshot
What Season Is It Anyway? Circadian Tracking vs. Photoperiodic Anticipation in Insects
inferredcites →https://doi.org/10.1177/0748730411414264openalex-snapshot
A New ImageJ Plug-in “ActogramJ” for Chronobiological Analyses
inferredcites →https://doi.org/10.1177/0748730414568430openalex-snapshot
Expression of Clock Genes period and timeless in the Central Nervous System of the Mediterranean Flour Moth, Ephestia kuehniella
inferredcites →https://doi.org/10.1177/074873048900400209openalex-snapshot
Latitudinal Clines in the Properties of a Circadian Pacemaker
inferredcites →https://doi.org/10.1186/1740-3391-5-1openalex-snapshot
Effects of altitude on circadian rhythm of adult locomotor activity in Himalayan strains of Drosophila helvetica
inferredcites →https://doi.org/10.1371/journal.pgen.1003534openalex-snapshot
A Genome-Wide, Fine-Scale Map of Natural Pigmentation Variation in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pone.0060167openalex-snapshot
Circadian Rhythms Differ between Sexes and Closely Related Species of Nasonia Wasps
inferredcites →https://doi.org/10.14411/eje.2003.042openalex-snapshot
Period gene expression in relation to seasonality and circadian rhythms in the linden bug, Pyrrhocoris apterus (Heteroptera)
inferredcites →https://doi.org/10.1534/genetics.107.079160openalex-snapshot
Circadian Rhythm Gene Regulation in the Housefly Musca domestica
inferredcites →https://doi.org/10.3109/01677069509084160openalex-snapshot
Ritsu: A Rhythm Mutant from a Natural Population ofDrosophila Melanogaster
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.5281/zenodo.16230928openalex-snapshot
Photoperiodic Responses of the Linden Bug, Pyrrhocoris apterus, under Conditions of Constant Temperature and under Thermoperiodic Conditions

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4065072openalex-extracted
Circadian-Period Variation Underlies the Local Adaptation of Photoperiodism in the Short-Day Plant Lemna aequinoctialis
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/s10164-025-00842-yopenalex-snapshot
Circadian rhythms of locomotor activity in the New World tarantula Neoholothele incei (Araneae: Theraphosidae)
inferred← citeshttps://doi.org/10.1016/j.cois.2017.12.005openalex-snapshot
By land, air, and sea: hemipteran diversity through the genomic lens
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.ibmb.2020.103376openalex-snapshot
Functional analysis and localisation of a thyrotropin-releasing hormone-type neuropeptide (EFLa) in hemipteran insects
inferred← citeshttps://doi.org/10.1016/j.ibmb.2022.103721openalex-snapshot
Sexual dimorphism of diapause regulation in the hemipteran bug Pyrrhocoris apterus
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.ibmb.2026.104589openalex-snapshot
Photoperiod induces sex-specific immune priming in Pyrrhocoris apterus
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104634openalex-snapshot
Circadian-period variation underlies the local adaptation of photoperiodism in the short-day plant Lemna aequinoctialis
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112338openalex-snapshot
Coevolution of Drosophila-type timeless with partner clock proteins
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2018.10.006openalex-snapshot
Supercooling and freezing as eco-physiological alternatives rather than mutually exclusive strategies: A case study in Pyrrhocoris apterus
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.06.003openalex-snapshot
The fitness benefits of genetic variation in circadian clock regulation
inferred← citeshttps://doi.org/10.1038/s41598-017-15014-3openalex-snapshot
A damping circadian clock drives weak oscillations in metabolism and locomotor activity of aphids (Acyrthosiphon pisum)
inferred← citeshttps://doi.org/10.1093/molbev/msaa048openalex-snapshot
Complex Evolution of Insect Insulin Receptors and Homologous Decoy Receptors, and Functional Significance of Their Multiplicity
inferred← citeshttps://doi.org/10.1093/molbev/msab346openalex-snapshot
Loss of Timeless Underlies an Evolutionary Transition within the Circadian Clock
inferred← citeshttps://doi.org/10.1111/ejn.16535openalex-snapshot
Circadian clock period length is not consistently linked to chronotype in a wild songbird
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/mve.12747openalex-snapshot
Intra‐species quantification reveals differences in activity and sleep levels in the yellow fever mosquito, Aedes aegypti
inferred← citeshttps://doi.org/10.1111/pce.14377openalex-snapshot
Naturally segregating genetic variation in circadian period exhibits a regional elevational and climatic cline
inferred← citeshttps://doi.org/10.1111/phen.12197openalex-snapshot
The role of circadian clock genes in the photoperiodic timer of the linden bug P yrrhocoris apterus during the nymphal stage
inferred← citeshttps://doi.org/10.1111/phen.12274openalex-snapshot
Roles of the circadian clock and endocrine regulator in the photoperiodic response of the brown‐winged green bug Plautia stali
inferred← citeshttps://doi.org/10.1177/0748730418764525openalex-snapshot
Circadian Rhythms and Reproductive Phenology Covary in a Natural Plant Population
inferred← citeshttps://doi.org/10.1242/jeb.243000openalex-snapshot
Cryptochrome-dependent magnetoreception in a heteropteran insect continues even after 24 h in darkness
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010924openalex-snapshot
Steroid receptor coactivator TAIMAN is a new modulator of insect circadian clock
inferred← citeshttps://doi.org/10.1371/journal.pone.0245115openalex-snapshot
Amplitude of circadian rhythms becomes weaken in the north, but there is no cline in the period of rhythm in a beetle
inferred← citeshttps://doi.org/10.14411/eje.2022.048openalex-snapshot
North vs. South: Contrasting patterns in the phenotypic plasticity of the firebug Pyrrhocoris apterus (Hemiptera: Pyrrhocoridae) at the latitudinal extremes of its distribution range
inferred← citeshttps://doi.org/10.2108/zs210081openalex-snapshot
Involvement of the Clock Gene Period in the Photoperiodism of the Silkmoth Bombyx mori
inferred← citeshttps://doi.org/10.3389/fphys.2019.00891openalex-snapshot
CRISPR/Cas9 Genome Editing Introduction and Optimization in the Non-model Insect Pyrrhocoris apterus
inferred← citeshttps://doi.org/10.3389/fphys.2019.01442openalex-snapshot
New Drosophila Circadian Clock Mutants Affecting Temperature Compensation Induced by Targeted Mutagenesis of Timeless
inferred← citeshttps://doi.org/10.3389/fphys.2020.00242openalex-snapshot
Light and Temperature Synchronizes Locomotor Activity in the Linden Bug, Pyrrhocoris apterus
inferred← citeshttps://doi.org/10.3389/fphys.2022.884909openalex-snapshot
Pigment Dispersing Factor Is a Circadian Clock Output and Regulates Photoperiodic Response in the Linden Bug, Pyrrhocoris apterus
inferred← citeshttps://doi.org/10.3390/bs9110115openalex-snapshot
Latitudinal Variation in Circadian Rhythmicity in Nasonia vitripennis
inferred← citeshttps://doi.org/10.3390/insects9040144openalex-snapshot
Climatic Variation of Supercooling Point in the Linden Bug Pyrrhocoris apterus (Heteroptera: Pyrrhocoridae)
inferred← citeshttps://doi.org/10.64898/2026.04.27.721165openalex-snapshot
Photoperiod induces sex-specific immune priming in Pyrrhocoris apterus
inferred← citeshttps://doi.org/10.64898/2026.09.29.754759openalex-snapshot
Fruit flies of the subgenera Drosophila , Siphlodora and Sophophora use different mechanisms to adapt their daily activity to long photoperiods
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