Latitudinal clines: an evolutionary view on biological rhythms,

A Mutant Drosophila Insulin Receptor Homolog That Extends Life-Span and Impairs Neuroendocrine Function

Tatar, M., Kopelman, A. H., Epstein, D., Tu, M., Yin, C. ‐., & Garofalo, R. S. (2001) · Science · doi:10.1126/science.1057987 · Cited by 1,630 · see citing works

Seasonal Adaptations of Insects

Taylor, L. R., Tauber, M. J., Tauber, C. A., & Masaki, S. (1987) · Journal of Animal Ecology · doi:10.2307/4831 · Cited by 1,586 · see citing works

Seasonal Adaptations of Insects

Tauber, M. J., Tauber, C. A., & Masaki, S. (1985) · Cited by 1,438 · see citing works

Insect dormancy: an ecological perspective.

Danks, H. V. (1987) · Medical Entomology and Zoology · Cited by 1,278 · see citing works

Temporal Organization: Reflections of a Darwinian Clock-Watcher

Pittendrigh, C. S. (1993) · Annual Review of Physiology · doi:10.1146/annurev.ph.55.030193.000313 · Cited by 1,023 · see citing works

FKF1 and GIGANTEA Complex Formation Is Required for Day-Length Measurement in Arabidopsis

Sawa, M., Nusinow, D. A., Kay, S. A., & Imaizumi, T. (2007) · Science · doi:10.1126/science.1146994 · Cited by 912 · see citing works

Insect overwintering in a changing climate

Bale, J. S., & Hayward, S. A. L. (2010) · Journal of Experimental Biology · doi:10.1242/jeb.037911 · Cited by 872 · see citing works

Photoperiodism and seasonal development of insects.

Danilevskiĭ, A. S. (1965) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.10741286 · Cited by 851 · see citing works

Resonating circadian clocks enhance fitness in cyanobacteria

Ouyang, Y., Andersson, C. R., Kondo, T., Golden, S. S., & Johnson, C. H. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.15.8660 · Cited by 772 · see citing works

Genetic shift in photoperiodic response correlated with global warming

Bradshaw, W. E., & Holzapfel, C. M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.241391498 · Cited by 645 · see citing works

Biological clocks in seasonal reproductive cycles

Follett, B. K., & Follett, D. E. (1981) · Medical Entomology and Zoology · Cited by 461 · see citing works

Enhanced Fitness Conferred by Naturally Occurring Variation in the Circadian Clock

Michael, T. P., Salomé, P. A., Yu, H. J., Spencer, T. R., Sharp, E. L., McPeek, M. A., Alonso, J. M., Ecker, J. R., & McClung, C. R. (2003) · Science · doi:10.1126/science.1082971 · Cited by 458 · see citing works

51. Erwin Bünning: Die endonome Tagesrhythmik als Grundlage der photoperiodischen Reaktion

(1936) · Berichte der Deutschen Botanischen Gesellschaft · doi:10.1111/j.1438-8677.1937.tb01941.x · Cited by 440 · see citing works

Insulin signaling and FOXO regulate the overwintering diapause of the mosquito Culex pipiens

Sim, C., & Denlinger, D. L. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802067105 · Cited by 412 · see citing works

<i>mPer1</i> and <i>mPer2</i> Are Essential for Normal Resetting of the Circadian Clock

Albrecht, U., Zheng, B., Larkin, D., Sun, Z. S., & Lee, C. C. (2001) · Journal of Biological Rhythms · doi:10.1177/074873001129001791 · Cited by 375 · see citing works

Circadian rhythms of locomotor activity in captive birds and mammals: Their variations with season and latitude

Daan, S., & Aschoff, J. (1975) · Oecologia · doi:10.1007/bf00345851 · Cited by 348 · see citing works

Natural Variation in a Drosophila Clock Gene and Temperature Compensation

Sawyer, L., Hennessy, J. M., Peixoto, A. A., Rosato, E., Parkinson, H., Costa, R., & Kyriacou, C. P. (1997) · Science · doi:10.1126/science.278.5346.2117 · Cited by 320 · see citing works

Ageing in Drosophila: The role of the insulin/Igf and TOR signalling network

Partridge, L., Alic, N., Bjedov, I., & Piper, M. D. W. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.09.003 · Cited by 318 · see citing works

Natural Selection Favors a Newly Derived <i>timeless</i> Allele in <i>Drosophila melanogaster</i>

Tauber, E., Zordan, M., Sandrelli, F., Pegoraro, M., Osterwalder, N., Breda, C., Daga, A., Selmin, A., Monger, K., Benna, C., et al. (2007) · Science · doi:10.1126/science.1138412 · Cited by 308 · see citing works

A molecular switch for photoperiod responsiveness in mammals

Dardente, H., Wyse, C. A., Birnie, M. J., Dupré, S. M., Loudon, A. S. I., Lincoln, G. A., & Hazlerigg, D. G. (2010) · Current Biology · doi:10.1016/j.cub.2010.10.048 · Cited by 291 · see citing works

GEOGRAPHIC VARIATION IN DIAPAUSE INCIDENCE, LIFE‐HISTORY TRAITS, AND CLIMATIC ADAPTATION INDROSOPHILA MELANOGASTER

SCHMIDT, P. S., Matzkin, L. M., Ippolito, M., & Eanes, W. F. (2005) · Evolution · doi:10.1111/j.0014-3820.2005.tb01821.x · Cited by 290 · see citing works

Network Features of the Mammalian Circadian Clock

Baggs, J. E., Price, T. S., DiTacchio, L., Panda, S., FitzGerald, G. A., & Hogenesch, J. B. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000052 · Cited by 265 · see citing works

Light, Time, and the Physiology of Biotic Response to Rapid Climate Change in Animals

Bradshaw, W. E., & Holzapfel, C. M. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135837 · Cited by 245 · see citing works

Evolution of time-keeping mechanisms: early emergence and adaptation to photoperiod

Hut, R. A., & Beersma, D. G. M. (2011) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2010.0409 · Cited by 222 · see citing works

Photoperiodic diapause under the control of circadian clock genes in an insect

Ikeno, T., Tanaka, S., Numata, H., & Goto, S. G. (2010) · BMC Biology · doi:10.1186/1741-7007-8-116 · Cited by 211 · see citing works

A Molecular Basis for Natural Selection at the <i>timeless</i> Locus in <i>Drosophila melanogaster</i>

Sandrelli, F., Tauber, E., Pegoraro, M., Mazzotta, G., Cisotto, P., Landskron, J., Stanewsky, R., Piccin, A., Rosato, E., Zordan, M., et al. (2007) · Science · doi:10.1126/science.1138426 · Cited by 205 · see citing works

An amino acid polymorphism in the couch potato gene forms the basis for climatic adaptation in Drosophila melanogaster

SCHMIDT, P. S., Zhu, C.-T., Das, J., Batavia, M., Yang, L., & Eanes, W. F. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805485105 · Cited by 199 · see citing works

Complications of complexity: integrating environmental, genetic and hormonal control of insect diapause

Emerson, K. J., Bradshaw, W. E., & Holzapfel, C. M. (2009) · Trends in Genetics · doi:10.1016/j.tig.2009.03.009 · Cited by 197 · see citing works

Natural variation in Drosophila melanogaster diapause due to the insulin-regulated PI3-kinase

Williams, K. D., Busto, M., Suster, M. L., So, A. K.-C., Ben‐Shahar, Y., Leevers, S. J., & Sokolowski, M. B. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604592103 · Cited by 169 · see citing works

A latitudinal cline in aDrosophilaclock gene

Costa, R., Peixoto, A. A., Barbujani, G., & Kyriacou, C. P. (1992) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1992.0128 · Cited by 168 · see citing works

The Amplitude of Circadian Oscillations: Temperature Dependence, Latitudinal Clines, and the Photoperiodic Time Measurement

Pittendrigh, C. S., Kyner, W. T., & Takamura, T. (1991) · Journal of Biological Rhythms · doi:10.1177/074873049100600402 · Cited by 155 · see citing works

Geographical variation in circadian eclosion rhythm and photoperiodic adult diapause inDrosophila littoralis

Lankinen, P. (1986) · Journal of Comparative Physiology A · doi:10.1007/bf00612503 · Cited by 153 · see citing works

Geography of photoperiodic response in diapausing mosquito

Bradshaw, W. E. (1976) · Nature · doi:10.1038/262384b0 · Cited by 152 · see citing works

Evidence that the TIM Light Response Is Relevant to Light-Induced Phase Shifts in Drosophila melanogaster

Suri, V., Qian, Z., Hall, J. C., & Rosbash, M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80529-2 · Cited by 148 · see citing works

AvianClockgene polymorphism: evidence for a latitudinal cline in allele frequencies

Johnsen, A., Fidler, A. E., Kuhn, S., Carter, K. L., Hoffmann, A. A., Barr, I. R., Biard, C., Charmantier, A., Eens, M., Korsten, P., et al. (2007) · Molecular Ecology · doi:10.1111/j.1365-294x.2007.03552.x · Cited by 138 · see citing works

Thermoperiodic Control of Diapause in an Insect: Theory of Internal Coincidence

Saunders, D. S. (1973) · Science · doi:10.1126/science.181.4097.358 · Cited by 136 · see citing works

Roles of circadian clock genes in insect photoperiodism

Goto, S. G. (2012) · Entomological Science · doi:10.1111/ens.12000 · Cited by 131 · see citing works

Larval Diapause of Maternal Origin: Induction of Diapause in Nasonia Vitripennis (Walk.) (Hymenoptera: Pteromalidae)

Saunders, D. S. (1965) · Journal of Experimental Biology · doi:10.1242/jeb.42.3.495 · Cited by 125 · see citing works

Response of the Timeless Protein to Light Correlates with Behavioral Entrainment and Suggests a Nonvisual Pathway for Circadian Photoreception

Yang, Z., Emerson, M. M., Su, H. S., & Sehgal, A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80528-0 · Cited by 123 · see citing works

GEOGRAPHIC VARIATION IN DIAPAUSE INCIDENCE, LIFE-HISTORY TRAITS, AND CLIMATIC ADAPTATION IN DROSOPHILA MELANOGASTER

SCHMIDT, P. S., Matzkin, L. M., Ippolito, M., et al. (2005) · Evolution · doi:10.1554/05-115.1 · Cited by 123 · see citing works

Identification of a candidate adaptive polymorphism forDrosophilalife history by parallel independent clines on two continents

Paaby, A. B., Blacket, M. J., Hoffmann, A. A., & SCHMIDT, P. S. (2010) · Molecular Ecology · doi:10.1111/j.1365-294x.2009.04508.x · Cited by 122 · see citing works

Genetic Differences in Human Circadian Clock Genes among Worldwide Populations

Ciarleglio, C. M., Ryckman, K. K., Servick, S. V., Hida, A., Robbins, S., Wells, N., Hicks, J., Larson, S. A., Wiedermann, J. P., Carver, K., et al. (2008) · Journal of Biological Rhythms · doi:10.1177/0748730408320284 · Cited by 120 · see citing works

Acute Induction of Eya3 by Late-Night Light Stimulation Triggers TSHβ Expression in Photoperiodism

Masumoto, K.-H., Ukai-Tadenuma, M., Kasukawa, T., Nagano, M., Uno, K. D., Tsujino, K., Horikawa, K., Shigeyoshi, Y., & Ueda, H. R. (2010) · Current Biology · doi:10.1016/j.cub.2010.11.038 · Cited by 118 · see citing works

A latitudinal cline in the Chinook salmon ( <i>Oncorhynchus tshawytscha</i> ) <i>Clock</i> gene: evidence for selection on PolyQ length variants

O'Malley, K. G., & Banks, M. A. (2008) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2008.0524 · Cited by 111 · see citing works

Phase and Period Responses of the Circadian System of Mice (Mus musculus) to Light Stimuli of Different Duration

Comas, M., Beersma, D. G. M., Spoelstra, K., & Daan, S. (2006) · Journal of Biological Rhythms · doi:10.1177/0748730406292446 · Cited by 109 · see citing works

Circadian clock genes period and cycle regulate photoperiodic diapause in the bean bug Riptortus pedestris males

Ikeno, T., Numata, H., & Goto, S. G. (2011) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2011.04.006 · Cited by 107 · see citing works

Evolution of critical day length for diapause induction enables range expansion of Diorhabda carinulata , a biological control agent against tamarisk ( Tamarix spp.)

Bean, D. W., Dalin, P., & Dudley, T. L. (2012) · Evolutionary Applications · doi:10.1111/j.1752-4571.2012.00262.x · Cited by 101 · see citing works

Adaptive latitudinal cline of photoperiodic diapause induction in the parasitoid Nasonia vitripennis in Europe

Paolucci, S., van de Zande, L., & Beukeboom, L. W. (2013) · Journal of Evolutionary Biology · doi:10.1111/jeb.12113 · Cited by 100 · see citing works

Photoperiodic Induction of Diapause Requires Regulated Transcription of timeless in the Larval Brain of Chymomyza costata

Stehlík, J., Závodská, R., Shimada, K., Šauman, I., & Košťál, V. (2008) · Journal of Biological Rhythms · doi:10.1177/0748730407313364 · Cited by 98 · see citing works

<i>Clock</i> polymorphism in Pacific salmon: evidence for variable selection along a latitudinal gradient

O'Malley, K. G., Ford, M. J., & Hard, J. J. (2010) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2010.0762 · Cited by 97 · see citing works

Deciphering time measurement: The role of circadian ‘clock’ genes and formal experimentation in insect photoperiodism

Saunders, D. S., & Bertossa, R. C. (2011) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2011.01.013 · Cited by 94 · see citing works

Latitudinal Clines in the Properties of a Circadian Pacemaker

Pittendrigh, C. S., & Takamura, T. (1989) · Journal of Biological Rhythms · doi:10.1177/074873048900400209 · Cited by 91 · see citing works

Photoperiodic response requires mammalian-type cryptochrome in the bean bug Riptortus pedestris

Ikeno, T., Numata, H., & Goto, S. G. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.05.142 · Cited by 91 · see citing works

Circadian Rhythmicity and Photoperiodism in the Pitcher‐Plant Mosquito: Adaptive Response to the Photic Environment or Correlated Response to the Seasonal Environment?

Bradshaw, W. E., Quebodeaux, M. C., & Holzapfel, C. M. (2003) · The American Naturalist · doi:10.1086/374344 · Cited by 90 · see citing works

Geographic variation in critical photoperiod and in diapause intensity of Chrysopa carnea (Neuroptera)

Tauber, M. J., & Tauber, C. A. (1972) · Journal of Insect Physiology · doi:10.1016/0022-1910(72)90061-3 · Cited by 85 · see citing works

The hormonal and circadian basis for insect photoperiodic timing

Schiesari, L., Kyriacou, C. P., & Costa, R. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.02.026 · Cited by 82 · see citing works

Quantitative Trait Loci Associated with Photoperiodic Response and Stage of Diapause in the Pitcher-Plant Mosquito, Wyeomyia smithii

Mathias, D. K., Jacky, L., Bradshaw, W. E., & Holzapfel, C. M. (2007) · Genetics · doi:10.1534/genetics.106.068726 · Cited by 82 · see citing works

Adaptation to a seasonally varying environment: a strong latitudinal cline in reproductive diapause combined with high gene flow in Drosophila montana

Tyukmaeva, V. I., Salminen, T. S., Kankare, M., Knott, K. E., & Hoikkala, A. (2011) · Ecology and Evolution · doi:10.1002/ece3.14 · Cited by 80 · see citing works

Independence of Genetic Geographical Variation between Photoperiodic Diapause, Circadian Eclosion Rhythm, and Thr-Gly Repeat Region of the Period Gene in Drosophila littoralis

Lankinen, P., & Forsman, P. (2006) · Journal of Biological Rhythms · doi:10.1177/0748730405283418 · Cited by 73 · see citing works

Geographic variability in diapause response of Japanese Orius species

Shimizu, T., & KAWASAKI, K. (2001) · Entomologia Experimentalis et Applicata · doi:10.1046/j.1570-7458.2001.00787.x · Cited by 72 · see citing works

Seasonal adaptations of the fall webworm Hyphantria cunea (Drury) (Lepidoptera: Arctiidae) following its invasion of Japan

Gomi, T. (2007) · Ecological Research · doi:10.1007/s11284-006-0327-y · Cited by 71 · see citing works

The required day number and timely induction of diapause in geographic strains of the mosquito Aedes atropalpus

Beach, R. (1978) · Journal of Insect Physiology · doi:10.1016/0022-1910(78)90088-4 · Cited by 66 · see citing works

Association between Circadian Clock Genes and Diapause Incidence in Drosophila triauraria

Yamada, H., & Yamamoto, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027493 · Cited by 66 · see citing works

Twilights Widen the Range of Photic Entrainment in Hamsters

Boulos, Z., Macchi, M. M., & Terman, M. (2002) · Journal of Biological Rhythms · doi:10.1177/074873002129002654 · Cited by 66 · see citing works

Insect circadian rhythms and photoperiodism

Saunders, D. S. (1997) · Invertebrate Neuroscience · doi:10.1007/bf02480370 · Cited by 65 · see citing works

Conceptual translation of timeless reveals alternative initiating methionines in Drosophila

Rosato, E. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.3.455 · Cited by 64 · see citing works

The period Gene Thr-Gly Polymorphism in Australian and African Drosophila melanogaster Populations: Implications for Selection

Sawyer, L., Sandrelli, F., Pasetto, C., Peixoto, A. A., Rosato, E., Costa, R., & Kyriacou, C. P. (2006) · Genetics · doi:10.1534/genetics.106.058792 · Cited by 58 · see citing works

Linkage disequilibrium, mutational analysis and natural selection in the repetitive region of the clock gene, period, in Drosophila melanogaster

Rosato, E., Peixoto, A. A., Costa, R., & Kyriacou, C. P. (1997) · Genetics Research · doi:10.1017/s001667239700267x · Cited by 56 · see citing works

North–south differences in circadian eclosion rhythm in European populations of Drosophila subobscura

Lankinen, P. (1993) · Heredity · doi:10.1038/hdy.1993.126 · Cited by 55 · see citing works

Scotopic vision in colour-blinds

Verhulst, S., & Maes, F. W. (1998) · Vision Research · doi:10.1016/s0042-6989(97)00339-8 · Cited by 52 · see citing works

Photoperiodism: Shall EYA Compare Thee to a Summer's Day?

Hut, R. A. (2011) · Current Biology · doi:10.1016/j.cub.2010.11.060 · Cited by 52 · see citing works

Zum Einfluß der Dämmerung auf die circadiane Periodik

Wever, R. (1967) · Zeitschrift für Vergleichende Physiologie · doi:10.1007/bf00349602 · Cited by 51 · see citing works

Geographic variation in diapause induction and mode of diapause inheritance in Tetranychus pueraricola

Suwa, A., & Gotoh, T. (2006) · Journal of Applied Entomology · doi:10.1111/j.1439-0418.2006.01050.x · Cited by 51 · see citing works

The circadian rhythm of oviposition inDrosophila melanogaster: A genetic latitudinal cline in wild populations

Allemand, R., & David, J. R. (1976) · Cellular and Molecular Life Sciences · doi:10.1007/bf01937401 · Cited by 50 · see citing works

Mendelian Inheritance of Pupal Diapause in the Flesh Fly, Sarcophaga bullata

Han, B., & Denlinger, D. L. (2008) · Journal of Heredity · doi:10.1093/jhered/esn082 · Cited by 49 · see citing works

Evolution of photoperiodic time measurement is independent of the circadian clock in the pitcher-plant mosquito, Wyeomyia smithii

Emerson, K. J., Dake, S. J., Bradshaw, W. E., & Holzapfel, C. M. (2009) · Journal of Comparative Physiology A · doi:10.1007/s00359-009-0416-9 · Cited by 48 · see citing works

Seasonal Adaptations of Insects as Revealed by Latitudinal Diapause Clines

Masaki, S. (1999) · Institutional Repositories DataBase (IRDB) · Cited by 47 · see citing works

PATTERNS OF PHENOTYPIC AND GENETIC VARIATION FOR THE PLASTICITY OF DIAPAUSE INCIDENCE

Winterhalter, W. E., & Mousseau, T. A. (2007) · Evolution · doi:10.1111/j.1558-5646.2007.00127.x · Cited by 45 · see citing works

Genetic Correlation between Circadian Eclosion Rhythm and Photoperiodic Diapause in Drosophila littoralis

Lankinen, P. (1986) · Journal of Biological Rhythms · doi:10.1177/074873048600100202 · Cited by 42 · see citing works

Maternal temperature has different effects on the photoperiodic response and duration of larval diapause in blow fly (Calliphora vicina) strains collected at two latitudes

McWatters, H. G., & Saunders, D. S. (1998) · Physiological Entomology · doi:10.1046/j.1365-3032.1998.00101.x · Cited by 42 · see citing works

Maternal temperature has different effects on the photoperiodic response and duration of larval diapause in blow fly ( Calliphora vicina ) strains collected at two latitudes

McWatters, H. G., & Saunders, D. S. (1998) · Physiological Entomology · doi:10.1046/j.1365-3032.1998.234101.x · Cited by 41 · see citing works

Strong pituitary and hypothalamic responses to photoperiod but not to 6-methoxy-2-benzoxazolinone in female common voles (Microtus arvalis)

Król, E., Douglas, A., Dardente, H., Birnie, M. J., van der Vinne, V., Eijer, W. G., Gerkema, M. P., Hazlerigg, D. G., & Hut, R. A. (2012) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2012.09.004 · Cited by 41 · see citing works

Rapid seasonal adaptation of an alien bruchid after introduction: geographic variation in life cycle synchronization and critical photoperiod for diapause induction

Sadakiyo, S., & Ishihara, M. (2011) · Entomologia Experimentalis et Applicata · doi:10.1111/j.1570-7458.2011.01136.x · Cited by 40 · see citing works

A phase response curve for circannual rhythm in the varied carpet beetle Anthrenus verbasci

Miyazaki, Y., Nisimura, T., & Numata, H. (2005) · Journal of Comparative Physiology A · doi:10.1007/s00359-005-0012-6 · Cited by 40 · see citing works

Clock gene variation in Tachycineta swallows

Dor, R., Cooper, C. B., Lovette, I. J., Massoni, V., Bulit, F., Liljesthröm, M., & Winkler, D. W. (2011) · Ecology and Evolution · doi:10.1002/ece3.73 · Cited by 38 · see citing works

Length variation in a specific region of the period gene correlates with differences in pupal diapause incidence in the flesh fly, Sarcophaga bullata

Han, B., & Denlinger, D. L. (2009) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2009.01.005 · Cited by 38 · see citing works

Molecular and quantitative genetic differentiation across Europe in yellow dung flies

Demont, M., BLANCKENHORN, W. U., Hosken, D. J., & Garner, T. W. J. (2008) · Journal of Evolutionary Biology · doi:10.1111/j.1420-9101.2008.01615.x · Cited by 37 · see citing works

Comparative analysis of Avian BMAL1 and CLOCK protein sequences: a search for features associated with owl nocturnal behaviour

Fidler, A. E., & Gwinner, E. (2003) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/s1096-4959(03)00276-8 · Cited by 36 · see citing works

Season- and Latitude-Dependent Effects of Simulated Twilights on Circadian Entrainment

Boulos, Z., & Macchi, M. M. (2005) · Journal of Biological Rhythms · doi:10.1177/0748730404272907 · Cited by 35 · see citing works

Low Variation in the Polymorphic Clock Gene Poly-Q Region Despite Population Genetic Structure across Barn Swallow (Hirundo rustica) Populations

Dor, R., Lovette, I. J., Safran, R. J., Billerman, S. M., Huber, G. H., Vortman, Y., Lotem, A., McGowan, A., Evans, M. R., Cooper, C. B., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028843 · Cited by 35 · see citing works

Genetic diversity patterns at the human clock gene period 2 are suggestive of population-specific positive selection

Cruciani, F., Trombetta, B., Labuda, D., Modiano, D., Torroni, A., Costa, R., & Scozzari, R. (2008) · European Journal of Human Genetics · doi:10.1038/ejhg.2008.105 · Cited by 33 · see citing works

Geographic Variation of Photoperiodic Diapause but Not Adult Survival or Reproduction of the Invasive MosquitoAedes albopictus(Diptera: Culicidae) in North America

Leisnham, P. T., Towler, L., & Juliano, S. A. (2011) · Annals of the Entomological Society of America · doi:10.1603/an11032 · Cited by 30 · see citing works

Geographical variation in photoperiodic induction of larval diapause in the bruchid beetle, Bruchidius dorsalis: polymorphism in overwintering stages

Kurota, H., & Shimada, M. (2003) · Entomologia Experimentalis et Applicata · doi:10.1046/j.1570-7458.2003.00033.x · Cited by 29 · see citing works

Geographic variation in photoperiodic diapause induction and diapause intensity in Sericinus montelus (Lepidoptera: Papilionidae)

Wang, X., Yang, Q., Dalin, P., Zhou, X., Luo, Z., & Lei, C. (2011) · Insect Science · doi:10.1111/j.1744-7917.2011.01473.x · Cited by 27 · see citing works

Besonderheiten der Circadianen Rhythmik bei Pflanzen Verschiedener Geographischer Breiten

Mayer, W. (1966) · Planta · doi:10.1007/bf00396490 · Cited by 25 · see citing works

Effects of twilights on circadian entrainment patterns and reentrainment rates in squirrel monkeys

Boulos, Z., Macchi, M. M., & Terman, M. (1996) · Journal of Comparative Physiology A · doi:10.1007/bf00216132 · Cited by 25 · see citing works

GEOGRAPHICAL VARIATION IN THE REPRODUCTIVE CYCLE AND PHOTOPERIODIC DIAPAUSE OFDROSOPHILA PHALERATAANDD. TRANSVERSA(DROSOPHILIDAE:DIPTERA)

Muona, O., & Lumme, J. (1981) · Evolution · doi:10.1111/j.1558-5646.1981.tb04868.x · Cited by 25 · see citing works

Twilight and Photoperiod Affect Behavioral Entrainment in the House Mouse ( Mus musculus )

Comas, M., & Hut, R. A. (2009) · Journal of Biological Rhythms · doi:10.1177/0748730409343873 · Cited by 22 · see citing works

Er�rterungen zur definition und anwendbarkeit der begriffe ?ultimate factor?, ?proximate factor? und ?Zeitgeber?

Immelmann, K. (1972) · Oecologia · doi:10.1007/bf00345235 · Cited by 19 · see citing works

Human color vision deficiencies and atmospheric twilight

Reimchen, T. E. (1987) · Biodemography and Social Biology · doi:10.1080/19485565.1987.9988655 · Cited by 17 · see citing works

Testing for causality in covarying traits: genes and latitude in a molecular world

O’BRIEN, C., Bradshaw, W. E., & Holzapfel, C. M. (2011) · Molecular Ecology · doi:10.1111/j.1365-294x.2011.05133.x · Cited by 16 · see citing works

Geographic variation in photoperiodic diapause induction and diapause intensity in Sericinus montelus （Lepidoptera Papilionidae）

Xiaoping, Wang, Qiusheng, Yang, Y., Peter, P., Dalin, Xing-Miao, Zhou, Zhiwen, Luo, et al. (2012) · Acta Scientiarum Naturalium Universitatis Sunyatseni · Cited by 13 · see citing works

Circannual rhythm in the varied carpet beetle, Anthrenus verbasci

Miyazaki, Y., Nisimura, T., & Numata, H. (2012) · Progress in brain research · doi:10.1016/b978-0-444-59427-3.00025-3 · Cited by 11 · see citing works

Seasonal adaptations of different geographical populations of the sunflower moth, Homoeosoma electellum

Kikukawa, S., & CHIPPENDALE, G. M. (1984) · Journal of Insect Physiology · doi:10.1016/0022-1910(84)90024-6 · Cited by 11 · see citing works

Geographical Variation in the Reproductive Cycle and Photoperiodic Diapause of Drosophila phalerata and D. transversa (Drosophilidae:Diptera)

Muona, O., & Lumme, J. (1981) · Evolution · doi:10.2307/2407949 · Cited by 11 · see citing works

A latitudinal cline in the efficacy of endogenous signals: evidence derived from retinal cone contraction in fish

Yammouni, R., Bozzano, A., & Douglas, R. H. (2011) · Journal of Experimental Biology · doi:10.1242/jeb.048538 · Cited by 8 · see citing works

Adaptation to climate change through genetic accommodation and assimilation of plastic phenotypes

Kelly, M. W. (2019) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2018.0176 · Cited by 344 · see citing works

Annual rhythms that underlie phenology: biological time-keeping meets environmental change

Helm, B., Ben‐Shlomo, R., Sheriff, M. J., Hut, R. A., Foster, F., Barnes, B. M., & Dominoni, D. M. (2013) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2013.0016 · Cited by 309 · see citing works

Impacts of Artificial Light at Night on Biological Timings

Gaston, K. J., Davies, T. W., Nedelec, S. L., & Holt, L. (2017) · Annual Review of Ecology Evolution and Systematics · doi:10.1146/annurev-ecolsys-110316-022745 · Cited by 305 · see citing works

Circadian Entrainment to the Natural Light-Dark Cycle across Seasons and the Weekend

Stothard, E. R., McHill, A. W., Depner, C. M., Birks, B. R., Moehlman, T. M., Ritchie, H. K., Guzzetti, J. R., Chinoy, E. D., LeBourgeois, M. K., Axelsson, J., et al. (2017) · Current Biology · doi:10.1016/j.cub.2016.12.041 · Cited by 303 · see citing works

Insect Diapause

Denlinger, D. L. (2022) · Cambridge University Press eBooks · doi:10.1017/9781108609364 · Cited by 181 · see citing works

Adaptations to polar life in mammals and birds

Blix, A. S. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.120477 · Cited by 180 · see citing works

11 Pressing Research Questions on How Light Pollution Affects Biodiversity

Hölker, F., Bolliger, J., Davies, T. W., Giavi, S., Jechow, A., Kalinkat, G., Longcore, T., Spoelstra, K., Tidau, S., Visser, M. E., et al. (2021) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2021.767177 · Cited by 165 · see citing works

The cost of circadian desynchrony: Evidence, insights and open questions

West, A. C., & Bechtold, D. A. (2015) · BioEssays · doi:10.1002/bies.201400173 · Cited by 143 · see citing works

GPS Based Daily Activity Patterns in European Red Deer and North American Elk (Cervus elaphus): Indication for a Weak Circadian Clock in Ungulates

Ensing, E. P., Ciuti, S., de Wijs, F. A. L. M., Lentferink, D. H., ten Hoedt, A., Boyce, M. S., & Hut, R. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0106997 · Cited by 143 · see citing works

Diapause research in insects: historical review and recent work perspectives

Tougeron, K. (2019) · Entomologia Experimentalis et Applicata · doi:10.1111/eea.12753 · Cited by 135 · see citing works

How climate change affects the seasonal ecology of insect parasitoids

Tougeron, K., Jacques Brodeur, B., Lann, C. L., & van Baaren, J. (2019) · Ecological Entomology · doi:10.1111/een.12792 · Cited by 145 · see citing works

Unexpected diversity in socially synchronized rhythms of shorebirds

Bulla, M., Vâlcu, M., Dokter, A. M., Dondua, A. G., Kosztolányi, A., Rutten, A. L., Helm, B., Sandercock, B. K., Casler, B., Ens, B. J., et al. (2016) · Nature · doi:10.1038/nature20563 · Cited by 128 · see citing works

Keeping time without a spine: what can the insect clock teach us about seasonal adaptation?

Denlinger, D. L., Hahn, D. A., Merlin, C., Holzapfel, C. M., & Bradshaw, W. E. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0257 · Cited by 119 · see citing works

Genetic variation in circadian regulation of nocturnal stomatal conductance enhances carbon assimilation and growth

de Dios, V. R., Loik, M. E., Smith, R., Aspinwall, M. J., & Tissue, D. T. (2015) · Plant Cell & Environment · doi:10.1111/pce.12598 · Cited by 109 · see citing works

Circadian rhythm phase shifts and endogenous free-running circadian period differ between African-Americans and European-Americans

Eastman, C., Suh, C., Tomaka, V. A., & Crowley, S. (2015) · Scientific Reports · doi:10.1038/srep08381 · Cited by 97 · see citing works

Latitudinal cline of chronotype

Leocadio-Miguel, M. A., Louzada, F. M., Duarte, L. L., Areas, R. P., Alam, M., Freire, M. V., Fontenele-Araujo, J., Menna-Barreto, L., & Pedrazzoli, M. (2017) · Scientific Reports · doi:10.1038/s41598-017-05797-w · Cited by 99 · see citing works

Genetics of human longevity within an eco-evolutionary nature-nurture framework

Giuliani, C., Garagnani, P., & Franceschi, C. (2018) · Circulation Research · doi:10.1161/circresaha.118.312562 · Cited by 92 · see citing works

Local climate determines vulnerability to camouflage mismatch in snowshoe hares

Zímová, M., Sirén, A. P. K., Nowak, J. J., Bryan, A. M., Ivan, J. S., Morelli, T. L., Suhrer, S., Whittington, J., & Mills, L. S. (2019) · Global Ecology and Biogeography · doi:10.1111/geb.13049 · Cited by 88 · see citing works

Artificial light during the polar night disrupts Arctic fish and zooplankton behaviour down to 200 m depth

Berge, J., Geoffroy, M., Daase, M., Cottier, F. R., Priou, P., Cohen, J. H., Johnsen, G. H., McKee, D., Kostakis, I., Renaud, P. E., et al. (2020) · Communications Biology · doi:10.1038/s42003-020-0807-6 · Cited by 87 · see citing works

Animal clocks: when science meets nature

Kronfeld‐Schor, N., Bloch, G., & Schwartz, W. J. (2013) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2013.1354 · Cited by 87 · see citing works

Life history events of eelgrass Zostera marina L. populations across gradients of latitude and temperature

Blok, S., Olesen, B., & Krause‐Jensen, D. (2018) · Marine Ecology Progress Series · doi:10.3354/meps12479 · Cited by 84 · see citing works

The adaptive nature of the plant circadian clock in natural environments

Oravec, M. W., & Greenham, K. (2022) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiac337 · Cited by 79 · see citing works

Geographic Variation of Plant Circadian Clock Function in Natural and Agricultural Settings

Greenham, K., Lou, P., Puzey, J. R., Kumar, G., Arnevik, C., Farid, H., Willis, J. H., & McClung, C. R. (2016) · Journal of Biological Rhythms · doi:10.1177/0748730416679307 · Cited by 74 · see citing works

Adaptation of Circadian Neuronal Network to Photoperiod in High-Latitude European Drosophilids

Menegazzi, P., Benetta, E. D., Beauchamp, M., Schlichting, M., Steffan-Dewenter, I. D., & Helfrich‐Förster, C. (2017) · Current Biology · doi:10.1016/j.cub.2017.01.036 · Cited by 74 · see citing works

Mutations in EID1 and LNK2 caused light-conditional clock deceleration during tomato domestication

Müller, N. A., Zhang, L., Koornneef, M., & Jiménez‐Gómez, J. M. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1801862115 · Cited by 73 · see citing works

Singing from North to South: Latitudinal variation in timing of dawn singing under natural and artificial light conditions

Silva, A. D., & Kempenaers, B. (2017) · Journal of Animal Ecology · doi:10.1111/1365-2656.12739 · Cited by 72 · see citing works

Local adaptation of photoperiodic plasticity maintains life cycle variation within latitudes in a butterfly

Lindestad, O., Wheat, C. W., Nylin, S., & Gotthard, K. (2018) · Ecology · doi:10.1002/ecy.2550 · Cited by 67 · see citing works

Mechanisms and Consequences of Partial Migration in Insects

Menz, M. H. M., Reynolds, D. R., Gao, B., Hu, G., Chapman, J. W., & Wotton, K. R. (2019) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2019.00403 · Cited by 66 · see citing works

Timing as a sexually selected trait: the right mate at the right moment

Hau, M., Dominoni, D. M., Casagrande, S., Buck, C. L., Wagner, G., Hazlerigg, D. G., Greives, T., & Hut, R. A. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0249 · Cited by 64 · see citing works

QTL analysis of the photoperiodic response and clinal distribution of period alleles in Nasonia vitripennis

Paolucci, S., Salis, L., Vermeulen, C. J., Beukeboom, L. W., & van de Zande, L. (2016) · Molecular Ecology · doi:10.1111/mec.13802 · Cited by 62 · see citing works

Circadian Clock Components Offer Targets for Crop Domestication and Improvement

McClung, C. R. (2021) · Genes · doi:10.3390/genes12030374 · Cited by 59 · see citing works

A cross‐scale approach to unravel the molecular basis of plant phenology in temperate and tropical climates

Satake, A., Nagahama, A., & Sasaki, E. (2021) · New Phytologist · doi:10.1111/nph.17897 · Cited by 59 · see citing works

Photoperiodic time measurement, photoreception, and circadian clocks in insect photoperiodism

Goto, S. G. (2022) · Applied Entomology and Zoology · doi:10.1007/s13355-022-00785-7 · Cited by 58 · see citing works

Rhythms of behavior: are the times changin’?

Häfker, N. S., & Tessmar‐Raible, K. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.10.005 · Cited by 58 · see citing works

Annual rhythms of milk and milk fat and protein production in dairy cattle in the United States

Salfer, I. J., Dechow, C. D., & Harvatine, K. J. (2018) · Journal of Dairy Science · doi:10.3168/jds.2018-15040 · Cited by 56 · see citing works

The Light Wavelength Affects the Ontogeny of Clock Gene Expression and Activity Rhythms in Zebrafish Larvae

Rosa, V. D., Frigato, E., López‐Olmeda, J. F., Sánchez‐Vázquez, F. J., & Bertolucci, C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0132235 · Cited by 55 · see citing works

Complete genomes of Hairstreak butterflies, their speciation and nucleo-mitochondrial incongruence

Cong, Q., Shen, J., Borek, D., Robbins, R. K., Otwinowski, Z., & Grishin, N. V. (2016) · Scientific Reports · doi:10.1038/srep24863 · Cited by 54 · see citing works

Clocks in the Wild: Entrainment to Natural Light

Schmal, C., Herzel, H., & Myung, J. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00272 · Cited by 53 · see citing works

Opsin Clines in Butterflies Suggest Novel Roles for Insect Photopigments

Frentiu, F. D., Yuan, F., Savage, W. K., Bernard, G. D., Mullen, S. P., & Briscoe, A. D. (2014) · Molecular Biology and Evolution · doi:10.1093/molbev/msu304 · Cited by 52 · see citing works

A Theoretical Study on Seasonality

Schmal, C., Myung, J., Herzel, H., & Bordyugov, G. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00094 · Cited by 52 · see citing works

Circadian rhythms of European and African-Americans after a large delay of sleep as in jet lag and night work

Eastman, C., Tomaka, V. A., & Crowley, S. (2016) · Scientific Reports · doi:10.1038/srep36716 · Cited by 48 · see citing works

The reunion of two lineages of the Neotropical brown stink bug on soybean lands in the heart of Brazil

Soares, P. L., Cordeiro, E. M. G., Nanini, F., Omoto, C., & Corrêa, A. S. (2018) · Scientific Reports · doi:10.1038/s41598-018-20187-6 · Cited by 51 · see citing works

Explaining the sawtooth: latitudinal periodicity in a circadian gene correlates with shifts in generation number

Levy, R. C., Kozak, G. M., Wadsworth, C. B., Coates, B. S., & Dopman, E. B. (2014) · Journal of Evolutionary Biology · doi:10.1111/jeb.12562 · Cited by 50 · see citing works

Circadian clocks: an overview on its adaptive significance

Krittika, S., & Yadav, P. (2020) · Biological Rhythm Research · doi:10.1080/09291016.2019.1581480 · Cited by 50 · see citing works

Latitudinal clines in the timing and temperature‐sensitivity of photoperiodic reproductive diapause in Drosophila montana

Tyukmaeva, V. I., Lankinen, P., Kinnunen, J., Kauranen, H., & Hoikkala, A. (2020) · Ecography · doi:10.1111/ecog.04892 · Cited by 49 · see citing works

Spectres of Clock Evolution: Past, Present, and Yet to Come

Jabbur, M. L., & Johnson, C. H. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2021.815847 · Cited by 49 · see citing works

The cyanobacterial circadian clock follows midday in vivo and in vitro

Leypunskiy, E., LIN, J. L.-C., Yoo, H., Lee, U., Dinner, A. R., & Rust, M. J. (2017) · eLife · doi:10.7554/elife.23539 · Cited by 49 · see citing works

Calanus finmarchicus seasonal cycle and diapause in relation to gene expression, physiology, and endogenous clocks

Häfker, N. S., Teschke, M., Last, K. S., Pond, D. W., Hüppe, L., & Meyer, B. (2018) · Limnology and Oceanography · doi:10.1002/lno.11011 · Cited by 49 · see citing works

Photic Barriers to Poleward Range-shifts

Huffeldt, N. P. (2020) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2020.04.011 · Cited by 49 · see citing works

Marine artificial light at night: An empirical and technical guide

Tidau, S., Smyth, T., McKee, D., Wiedenmann, J., D’Angelo, C., Wilcockson, D. C., Ellison, A., Grimmer, A. J., Jenkins, S. R., Widdicombe, S., et al. (2021) · Methods in Ecology and Evolution · doi:10.1111/2041-210x.13653 · Cited by 45 · see citing works

Photoperiodic time measurement in insects

Doležel, D. (2014) · Current Opinion in Insect Science · doi:10.1016/j.cois.2014.12.002 · Cited by 48 · see citing works

Evaluating the Adaptive Fitness of Circadian Clocks and their Evolution

Jabbur, M. L., Dani, C., Spoelstra, K., Dodd, A. N., & Johnson, C. H. (2024) · Journal of Biological Rhythms · doi:10.1177/07487304231219206 · Cited by 50 · see citing works

Activity patterns and spatial co-occurrence of sympatric mammals in the moist temperate forest of the Kashmir Himalaya, India

Noor, A., Mir, Z. R., Veeraswami, G. G., & Habib, B. (2017) · Folia zoologica (Brno) · doi:10.25225/fozo.v66.i4.a4.2017 · Cited by 41 · see citing works

Marine biorhythms: bridging chronobiology and ecology

Bulla, M., Oudman, T., Bijleveld, A. I., Piersma, T., & Kyriacou, C. P. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0253 · Cited by 44 · see citing works

Seasonal Time Keeping in a Long-Distance Migrating Shorebird

Karagicheva, J., Нурланович, Р. Э., Dekinga, A., Brugge, M., Koolhaas, A., ten Horn, J., & Piersma, T. (2016) · Journal of Biological Rhythms · doi:10.1177/0748730416655929 · Cited by 43 · see citing works

Clinal population divergence in an adaptive parental environmental effect that adjusts seed banking

Lampei, C., Metz, J., & Tielbörger, K. (2017) · New Phytologist · doi:10.1111/nph.14436 · Cited by 43 · see citing works

Seasonal variation in UVA light drives hormonal and behavioural changes in a marine annelid via a ciliary opsin

Rajan, V. B. V., Häfker, N. S., Arboleda, E., Poehn, B., Gossenreiter, T., Gerrard, E. J., Hofbauer, M., Mühlestein, C., Bileck, A., Gerner, C., et al. (2021) · Nature Ecology & Evolution · doi:10.1038/s41559-020-01356-1 · Cited by 40 · see citing works

Inactive trout come out at night: behavioral variation, circadian activity, and fitness in the wild

Závorka, L., Aldvén, D., Näslund, J., Höjesjö, J., & Johnsson, J. I. (2016) · Ecology · doi:10.1002/ecy.1475 · Cited by 41 · see citing works

Flies as models for circadian clock adaptation to environmental challenges

Helfrich‐Förster, C., Bertolini, E., & Menegazzi, P. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14180 · Cited by 40 · see citing works

Seasonal effects on bipolar disorder: A closer look

Rosenthal, S. J., Josephs, T., Kovtun, O., & McCarty, R. C. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.05.017 · Cited by 39 · see citing works

In the darkness of the polar night, scallops keep on a steady rhythm

Tran, D., Sow, M., Camus, L., Ciret, P., Berge, J., & Massabuau, J. (2016) · Scientific Reports · doi:10.1038/srep32435 · Cited by 39 · see citing works

Standing geographic variation in eclosion time and the genomics of host race formation inRhagoletis pomonellafruit flies

Doellman, M. M., Egan, S. P., Ragland, G. J., Meyers, P. J., Hood, G. R., Powell, T. H. Q., Lazorchak, P., Hahn, D. A., Berlocher, S. H., Nosil, P., et al. (2018) · Ecology and Evolution · doi:10.1002/ece3.4758 · Cited by 37 · see citing works

Selection for reproduction under short photoperiods changes diapause-associated traits and induces widespread genomic divergence

Kauranen, H., Kinnunen, J., Hiillos, A., Lankinen, P., Hopkins, D. P., Wiberg, R. A. W., Ritchie, M. G., & Hoikkala, A. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.205831 · Cited by 36 · see citing works

Insect photoperiodism: Seasonal development on a revolving planet

Saunders, D. S. (2020) · European Journal of Entomology · doi:10.14411/eje.2020.038 · Cited by 37 · see citing works

Growing plants in fluctuating environments: why bother?

Matsubara, S. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/ery312 · Cited by 37 · see citing works

Variation in butterfly diapause duration in relation to voltinism suggests adaptation to autumn warmth, not winter cold

Lindestad, O., von Schmalensee, L., Lehmann, P., & Gotthard, K. (2020) · Functional Ecology · doi:10.1111/1365-2435.13525 · Cited by 37 · see citing works

A molecular‐genetic understanding of diapause in spider mites: current knowledge and future directions

Bryon, A., Kurlovs, A. H., Leeuwen, T. V., & Clark, R. M. (2017) · Physiological Entomology · doi:10.1111/phen.12201 · Cited by 36 · see citing works

Artificial light at night alters activity, body mass, and corticosterone level in a tropical anuran

Secondi, J., Mondy, N., Gippet, J. M. W., Touzot, M., Gardette, V., Guillard, L., & Lengagne, T. (2021) · Behavioral Ecology · doi:10.1093/beheco/arab044 · Cited by 36 · see citing works

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

Chodáková, L., Vaněčková, H., Provazník, J., Wu, B. C.-H., Pivarči, M., Peckova, O., Bazalová, O., Čada, Š., Kment, P., Kotwica‐Rolinska, J., et al. (2016) · Journal of Biological Rhythms · doi:10.1177/0748730416671213 · Cited by 36 · see citing works

Bacteria can anticipate the seasons: Photoperiodism in cyanobacteria

Jabbur, M. L., Bratton, B. P., & Johnson, C. H. (2024) · Science · doi:10.1126/science.ado8588 · Cited by 36 · see citing works

Digital biodiversity data sets reveal breeding phenology and its drivers in a widespread North American mammal

McLean, B. S., & Guralnick, R. (2020) · Ecology · doi:10.1002/ecy.3258 · Cited by 35 · see citing works

Genomic Patterns of Geographic Differentiation in Drosophila simulans

Sedghifar, A., Saelao, P., & Begun, D. J. (2016) · Genetics · doi:10.1534/genetics.115.185496 · Cited by 34 · see citing works

Assessing the effects of artificial light at night on biodiversity across latitude – Current knowledge gaps

Secondi, J., Davranche, A., Théry, M., Mondy, N., & Lengagne, T. (2019) · Global Ecology and Biogeography · doi:10.1111/geb.13037 · Cited by 34 · see citing works

Distinct Physiological Mechanisms Induce Latitudinal and Sexual Differences in the Photoperiodic Induction of Diapause in a Fly

Yamaguchi, K., & Goto, S. G. (2019) · Journal of Biological Rhythms · doi:10.1177/0748730419841931 · Cited by 33 · see citing works

Artificial light at night reverses monthly foraging pattern under simulated moonlight

Tidau, S., Whittle, J., Jenkins, S. R., & Davies, T. W. (2022) · Biology Letters · doi:10.1098/rsbl.2022.0110 · Cited by 33 · see citing works

Twilight length alters growth and flowering time in Arabidopsis via LHY / CCA1

Mehta, D., Scandola, S., Kennedy, C., Lummer, C., Gallo, M. C. R., Grubb, L. E., Tan, M., Scarpella, E., & Uhrig, R. G. (2024) · Science Advances · doi:10.1126/sciadv.adl3199 · Cited by 32 · see citing works

Mechanisms of temperature modulation in mammalian seasonal timing

van Rosmalen, L., van Dalum, J., Appenroth, D., Roodenrijs, R. T. M., de Wit, L., Hazlerigg, D. G., & Hut, R. A. (2021) · The FASEB Journal · doi:10.1096/fj.202100162r · Cited by 32 · see citing works

Variation in circadian rhythms is maintained among and within populations in Boechera stricta

Salmela, M. J., Greenham, K., Lou, P., McClung, C. R., Ewers, B. E., & Weinig, C. (2015) · Plant Cell & Environment · doi:10.1111/pce.12670 · Cited by 31 · see citing works

The fitness benefits of genetic variation in circadian clock regulation

Salmela, M. J., & Weinig, C. (2019) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2019.06.003 · Cited by 31 · see citing works

Natural Variation and Genetics of Photoperiodism in Wyeomyia smithii

Bradshaw, W. E., & Holzapfel, C. M. (2017) · Advances in genetics · doi:10.1016/bs.adgen.2017.09.002 · Cited by 30 · see citing works

Clockgene polymorphism, migratory behaviour and geographic distribution: a comparative study of trans‐Saharan migratory birds

Bazzi, G., Cecere, J. G., Caprioli, M., Gatti, E., Gianfranceschi, L., Podofillini, S., Possenti, C. D., Ambrosini, R., Saino, N., Spina, F., et al. (2016) · Molecular Ecology · doi:10.1111/mec.13913 · Cited by 29 · see citing works

Analysis of the circadian transcriptome of the Antarctic krill Euphausia superba

Biscontin, A., Martini, P. G. V., Costa, R., Kramer, A., Meyer, B., Kawaguchi, S., Teschke, M., & Pittà, C. D. (2019) · Scientific Reports · doi:10.1038/s41598-019-50282-1 · Cited by 28 · see citing works

Circadian regulation of diel vertical migration (DVM) and metabolism in Antarctic krill Euphausia superba

Piccolin, F., Pitzschler, L., Biscontin, A., Kawaguchi, S., & Meyer, B. (2020) · Scientific Reports · doi:10.1038/s41598-020-73823-5 · Cited by 28 · see citing works

Reduced human disturbance increases diurnal activity in wolves, but not Eurasian lynx

Smith, A. F., Kasper, K., Lazzeri, L., Schulte, M., Kudrenko, S., Say‐Sallaz, E., Churski, M., Shamovich, D., Obrizan, S., Domashevsky, S., et al. (2024) · Global Ecology and Conservation · doi:10.1016/j.gecco.2024.e02985 · Cited by 28 · see citing works

Interaction between photoperiod and variation in circadian rhythms in tomato

Xiang, Y., Sapir, T., Rouillard, P., Ferrand, M., & Jiménez‐Gómez, J. M. (2022) · BMC Plant Biology · doi:10.1186/s12870-022-03565-1 · Cited by 25 · see citing works

Integrating Diel Vertical Migrations of Bioluminescent Deep Scattering Layers Into Monitoring Programs

Chatzievangelou, D., Bahamón, N., Martini, S., Fernández, J. D. R., Riccobene, G., Tangherlini, M., Danovaro, R., Léo, F. C. D., Pirenne, B., & Aguzzi, J. (2021) · Frontiers in Marine Science · doi:10.3389/fmars.2021.661809 · Cited by 24 · see citing works

Life-History Evolution of Insects in Response to Climate Variation: Seasonal Timing Versus Thermal Physiology

Gotthard, K., Berger, D., & Rohner, P. T. (2025) · Annual Review of Entomology · doi:10.1146/annurev-ento-121423-013506 · Cited by 23 · see citing works

“The Environment is Everything That Isn't Me”: Molecular Mechanisms and Evolutionary Dynamics of Insect Clocks in Variable Surroundings

Rivas, G. B. D. S., Bauzer, L. G. S. D. R., & Meireles-Filho, A. C. A. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2015.00400 · Cited by 22 · see citing works

Differences in photoperiod‐induced diapause plasticity among different populations of the bark beetle I ps typographus and its predator T hanasimus formicarius

Schroeder, M. L., & Dalin, P. (2016) · Agricultural and Forest Entomology · doi:10.1111/afe.12189 · Cited by 22 · see citing works

Light regime affects the seasonal cycle of Antarctic krill (Euphausia superba): impacts on growth, feeding, lipid metabolism, and maturity

Höring, F., Teschke, M., Suberg, L. A., Kawaguchi, S., & Meyer, B. (2018) · Canadian Journal of Zoology · doi:10.1139/cjz-2017-0353 · Cited by 22 · see citing works

Evolution of butterfly seasonal plasticity driven by climate change varies across life stages

Nielsen, M. E., Nylin, S., Wiklund, C., & Gotthard, K. (2023) · Ecology Letters · doi:10.1111/ele.14280 · Cited by 21 · see citing works

Dew-worms in white nights: High-latitude light constrains earthworm (Lumbricus terrestris) behaviour at the soil surface

Nuutinen, V., Butt, K. R., Jauhiainen, L., Shipitalo, M. J., & Sirén, T. (2014) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2014.01.023 · Cited by 21 · see citing works

Differences in reproductive effort and sexual recruitment of the seagrass Zostera japonica between two geographic populations in northern China

Zhang, X., Zhou, Y., Xu, S., Wang, P., Zhao, P., Yue, S., Gu, R., Song, X., Xu, S., Liu, J., et al. (2020) · Marine Ecology Progress Series · doi:10.3354/meps13248 · Cited by 21 · see citing works

Photophysiological cycles in Arctic krill are entrained by weak midday twilight during the Polar Night

Cohen, J. H., Last, K. S., Charpentier, C. L., Cottier, F. R., Daase, M., Hobbs, L., Johnsen, G. H., & Berge, J. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001413 · Cited by 21 · see citing works

Integration of photoperiodic and temperature cues by the circadian clock to regulate insect seasonal adaptations

Hidalgo, S., & Chiu, J. C. (2023) · Journal of Comparative Physiology A · doi:10.1007/s00359-023-01667-1 · Cited by 19 · see citing works

Environmental entrainment demonstrates natural circadian rhythmicity in the cnidarian Nematostella vectensis

Tarrant, A. M., Helm, R. R., Levy, O., & Rivera, H. E. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.205393 · Cited by 18 · see citing works

A Perspective Emphasizing Circadian Rhythm Entrainment to Ensure Sustainable Crop Production in Controlled Environment Agriculture: Dynamic Use of LED Cues

Marie, T. R. J. G., Leonardos, E. D., Lanoue, J., Hao, X., Micallef, B. J., & Grodzinski, B. (2022) · Frontiers in Sustainable Food Systems · doi:10.3389/fsufs.2022.856162 · Cited by 18 · see citing works

An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression

Akiyama, T., Katsumura, T., Nakagome, S., Lee, S., Joh, K., Soejima, H., Fujimoto, K., Kimura, R., Ishida, H., Hanihara, T., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178373 · Cited by 18 · see citing works

Telling the Seasons Underground: The Circadian Clock and Ambient Temperature Shape Light Exposure and Photoperiodism in a Subterranean Rodent

Flôres, D. E. F. L., Jannetti, M. G., Improta, G. C., Tachinardi, P., Valentinuzzi, V. S., & Oda, G. A. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.738471 · Cited by 17 · see citing works

Circannual Cycles and Photoperiodism

Cassone, V. M., & Yoshimura, T. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-407160-5.00035-x · Cited by 17 · see citing works

Clines in clock genes: fine-tuning circadian rhythms to the environment

Kyriacou, C. P., Peixoto, A. A., Sandrelli, F., Costa, R., & Tauber, E. (2008) · Trends in Genetics · doi:10.1016/j.tig.2007.12.003 · Cited by 154 · see citing works

Latitudinal cline of chronotype

Leocadio-Miguel, M. A., Louzada, F. M., Duarte, L. L., Areas, R. P., Alam, M., Freire, M. V., Fontenele-Araujo, J., Menna-Barreto, L., & Pedrazzoli, M. (2017) · Scientific Reports · doi:10.1038/s41598-017-05797-w · Cited by 99 · see citing works

AvianClockgene polymorphism: evidence for a latitudinal cline in allele frequencies

Johnsen, A., Fidler, A. E., Kuhn, S., Carter, K. L., Hoffmann, A. A., Barr, I. R., Biard, C., Charmantier, A., Eens, M., Korsten, P., et al. (2007) · Molecular Ecology · doi:10.1111/j.1365-294x.2007.03552.x · Cited by 138 · see citing works

Genetic Differences in Human Circadian Clock Genes among Worldwide Populations

Ciarleglio, C. M., Ryckman, K. K., Servick, S. V., Hida, A., Robbins, S., Wells, N., Hicks, J., Larson, S. A., Wiedermann, J. P., Carver, K., et al. (2008) · Journal of Biological Rhythms · doi:10.1177/0748730408320284 · Cited by 120 · see citing works

“The Environment is Everything That Isn't Me”: Molecular Mechanisms and Evolutionary Dynamics of Insect Clocks in Variable Surroundings

Rivas, G. B. D. S., Bauzer, L. G. S. D. R., & Meireles-Filho, A. C. A. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2015.00400 · Cited by 22 · see citing works