Effects of Temperature on Circadian Clock and Chronotype: An Experimental Study on a Passerine Bird

REFERENCES

• Allebrandt KV, Roenneberg T. (2008). The search for circadian clock components in humans: new perspectives for association studies. Braz. J. Med. Biol. Res. 41:716–721.
   PubMed Web of Science ®Google Scholar
• Aschoff J. (1965). The phase-angle difference in circadian periodicity. In Aschoff J (ed.). Circadian clocks. Amsterdam: North-Holland, 262–276.
   Google Scholar
• Aschoff J. (1979). Circadian rhythms: influences of internal and external factors on the period measured in constant conditions. Z. Tierpsychol. 49:225–249.
   PubMedGoogle Scholar
• Aschoff J, Pohl H. (1978). Phase relations between a circadian rhythm and its zeitgeber within the range of entrainment. Naturwissenschaften 65:80–84.
   PubMed Web of Science ®Google Scholar
• Aschoff J, Wever R. (1962). Über Phasenbeziehungen zwischen biologischer Tagesperiodik und Zeitgeberperiodik. J. Comp. Physiol. 46:115–128.
   Google Scholar
• Aschoff J, Wever R. (1966). Circadian period and phase-angle difference in chaffinches (Fringilla coelebs L.). Comp. Biochem. Physiol. 18:397–404.
   PubMed Web of Science ®Google Scholar
• Bednekoff PA, Houston AI. (1994). Avian daily foraging patterns: effects of digestive constraints and variability. Evol. Ecol. 8:36–52.
   Web of Science ®Google Scholar
• Bednekoff PA, Krebs JR. (1995). Great Tit fat reserves: effects of changing and unpredictable feeding day length. Funct. Ecol. 9:457–462.
   Web of Science ®Google Scholar
• Bednekoff PA, Biebach H, Krebs J. (1994). Great Tit fat reserves under unpredictable temperatures. J. Avian Biol. 25:156–160.
   Web of Science ®Google Scholar
• Beersma DGM, van Bunnik BAD, Hut RA, Daan S. (2008). Emergence of circadian and photoperiodic system level properties from interactions among pacemaker cells. J. Biol. Rhythms 23:362–373.
   PubMed Web of Science ®Google Scholar
• Bertin A, Houdelier C, Richard-Yris M-A, Guyomarc'h C, Lumineau S. (2007). Stable individual profiles of daily timing of migratory restlessness in European quail. Chronobiol. Int. 24:253–267.
   PubMed Web of Science ®Google Scholar
• Brown SA, Kunz D, Dumas A, Westermark PO, Vanselow K, Tilmann-Wahnschaffe A, Herzel H, Kramer A. (2008). Molecular insights into human daily behavior. Proc. Natl. Acad. Sci. U. S. A. 105:1602–1607.
   PubMed Web of Science ®Google Scholar
• Charmantier A, McCleery RH, Cole LR, Perrins C, Kruuk LEB, Sheldon BC. (2008). Adaptive phenotypic plasticity in response to climate change in a wild bird population. Science 320:800–803.
   PubMed Web of Science ®Google Scholar
• Conover WJ, Iman RL. (1981). Rank transformations as a bridge between parametric and nonparametric statistics. Am. Stat. 35:124–129.
   Web of Science ®Google Scholar
• Daan S, Aschoff J. (1975). Circadian rhythms of locomotor activity in captive birds and mammals—their variations with season and latitude. Oecologia 18:269–316.
   PubMed Web of Science ®Google Scholar
• Daan S, Aschoff J. (1982). Circadian contributions to survival. In Aschoff J, Daan S, Groos GA (eds.). Vertebrate circadian systems: structure and physiology. Berlin: Springer-Verlag, 305–321.
   Google Scholar
• Daan S, Beersma DGM. (2002). Circadian frequency and its variability. In Kumar V (ed.). Biological rhythms. New Delhi: Narosa, 24–37.
   Google Scholar
• Dallmann R, DeBruyne JP, Weaver DR. (2011). Photic resetting and entrainment in CLOCK-deficient mice. J. Biol. Rhythms 26:390–401.
   PubMed Web of Science ®Google Scholar
• DeCoursey P. (1960). Phase control of activity in a rodent. Cold Spring Harbor Symp. Quant. Biol. 25:49–55.
   PubMedGoogle Scholar
• Dolan AC, Murphy MT, Redmond LJ, Sexton K, Duffield D. (2007). Extrapair paternity and the opportunity for sexual selection in a socially monogamous passerine. Behav. Ecol. 18:985–993.
   Web of Science ®Google Scholar
• Enright JT. (1966). Temperature and the free-running circadian rhythm of the house finch. J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 18:463–475.
   Google Scholar
• Fleissner G, Fleissner G. (2002). Perception of natural zeitgeber signals. In Kumar V(ed.). Biological rhythms. New-Delhi: Narosa, 83–93.
   Google Scholar
• Fleury F, Allemand R, Vavre F, Fouillet P, Bouletreau M. (2000). Adaptive significance of a circadian clock: temporal segregation of activities reduces intrinsic competitive inferiority in Drosophila parasitoids. Proc. Biol. Sci. 267:1005–1010.
   PubMed Web of Science ®Google Scholar
• Genstat. (1993). Genstat 5 release 3 reference manual. Oxford, UK: Clarendon Press.
   Google Scholar
• Gosler A. (1993). The great tit. London: Hamlyn, 128.
   Google Scholar
• Helm B, Gwinner E. (2005). Carry-over effects of day length during spring migration. J. Ornithol. 146:348–354.
   Web of Science ®Google Scholar
• Helm B, Visser ME. (2010). Heritable circadian period length in a wild bird population. Proc. Biol. Sci. 277:3335–3342.
   PubMed Web of Science ®Google Scholar
• Hinde RA. (1952). The behaviour of the Great tit (Parus major) and some other related species. Behav. Suppl. 2: III, V-X, 1–201.
   Google Scholar
• Husby A, Nussey DH, Visser ME, Wilson AJ, Sheldon BC, Kruuk LEB. (2010). Contrasting patterns of phenotypic plasticity in reproductive traits in two great tit (Parus major) populations. Evolution 64:2221–2237
   PubMed Web of Science ®Google Scholar
• Kacelnik A. (1979). The foraging efficiency of great tits (Parus major L.) in relation to light intensity. Anim. Behav. 27:237–241.
   Web of Science ®Google Scholar
• Kacelnik A, Krebs JR. (1982). The dawn chorus in the great tit (Parus major): proximate and ultimate causes. Behaviour 83:287–309.
   Web of Science ®Google Scholar
• Kempenaers B, Borgström P, Loës P, Schlicht E, Valcu M. (2010). Artificial night lighting affects dawn song, extra-pair siring success, and lay date in songbirds. Curr. Biol. 20:1735–1739.
   PubMed Web of Science ®Google Scholar
• Krams I, Cirule D, Suraka V, Krama T, Rantala MJ, Ramey G. (2010). Fattening strategies of wintering Great tits support the optimal body mass hypothesis under conditions of extremely low ambient temperature. Funct. Ecol. 24 172–177.
   Web of Science ®Google Scholar
• Kronfeld-Schor N, Dayan T. (2003). Partitioning of time as an ecological resource. Annu. Rev. Ecol. Evol. Syst. 34:153–181.
   Web of Science ®Google Scholar
• Lessells CM, Boag PT. (1987). Unrepeatable repeatabilities: a common mistake. The Auk 104:116–121.
   Web of Science ®Google Scholar
• Lynch M, Walsh B. (1998). Genetics and analysis of quantitative traits. Sunderland, MA: Sinauer, 980.
   Google Scholar
• Mace R. (1986). Importance of female behaviour in the dawn chorus. Anim. Behav. 34:621–622.
   Web of Science ®Google Scholar
• Menaker M. (2006). Circadian organization in the real world. Proc. Natl. Acad. Sci. U. S. A. 103:3015–3016.
   PubMed Web of Science ®Google Scholar
• Merrow M, Spoelstra K, Roenneberg T. (2005). The circadian cycle: daily rhythms from behaviour to genes. EMBO Rep. 6:930–935.
   PubMed Web of Science ®Google Scholar
• Moore D, Doherty P. (2009). Acquisition of a time-memory in forager honey bees. J. Comp. Physiol. Sens. Neu. Behav. Physiol. 195:741–751.
   PubMed Web of Science ®Google Scholar
• Murphy MT, Sexton K, Dolan AC, Redmond LJ. (2008). Dawn song of the Eastern Kingbird: an honest signal of male quality? Anim. Behav. 75:1075–1084.
   Web of Science ®Google Scholar
• Natale V, Di Milia L. (2011). Season of birth and morningness: comparison between the northern and southern hemisphere. Chronobiol. Int. 28:727–730.
   PubMed Web of Science ®Google Scholar
• Nussey DH, Postma E, Gienapp P, Visser ME. (2005). Selection on heritable phenotypic plasticity in a wild bird population. Science 310:304–306.
   PubMed Web of Science ®Google Scholar
• Poesel A, Kunc HP, Foerster K, Johnsen A, Kempenaers B. (2007). Early birds are sexy: male age, dawn song and extra-pair paternity in Blue tits, Cyanistes (formerly Parus) caeruleus. Anim. Behav. 72:531–538.
   Web of Science ®Google Scholar
• Pohl H. (1968). Einfluß der Temperatur auf die freilaufende circadiane Aktivitätsperiodik bei Warmblütern. J. Comp. Physiol. Sens. Neu. Behav. Physiol. 58:364–380.
   Google Scholar
• Pohl H. (1974). Interaction of effects of light, temperature and season on the circadian period of Carduelis flammea. Naturwissenschaften 61:406–407.
   PubMedGoogle Scholar
• Portaluppi F, Smolensky MH, Touitou Y. (2010). Ethics and methods for biological rhythm research on animals and human beings. Chronobiol. Int. 27:1911–1929.
   PubMed Web of Science ®Google Scholar
• R Development Core Team. (2012). R: a language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing. http://www.R-project.org/ Accessed 30 March 2012.
   Google Scholar
• Redlin U. (2001). Neural basis and biological function of masking by light in mammals: suppression of melatonin and locomotor activity. Chronobiol. Int. 18:737–758.
   PubMed Web of Science ®Google Scholar
• Rensing L, Ruoff P. (2002). Temperature effect on entrainment, phase shifting, and amplitude of circadian clocks and its molecular bases. Chronobiol. Int. 19:807–864.
   PubMed Web of Science ®Google Scholar
• Roenneberg T, Merrow M. (2007). Entrainment of the human circadian clock. Cold Spring Harbor Symp. Quant. Biol. 72:293–299.
   PubMedGoogle Scholar
• Roenneberg T, Kuehnle T, Juda M, Kantermann T, Allebrandt K, Gordijn M, Merrow M. (2007). Epidemiology of the human circadian clock. Sleep Med. Rev. 11:429–438.
   PubMed Web of Science ®Google Scholar
• Ruf T. (1999). The Lomb-Scargle periodogram in biological rhythm research: analysis of incomplete and unequally spaced time-series. Biol. Rhythm Res. 30:178–201.
   Web of Science ®Google Scholar
• Ruoff P, Rensing L. (2004). Temperature effects on circadian clocks. J. Therm. Biol. 29:445–456.
   Web of Science ®Google Scholar
• Sakai T, Ishida N. (2001). Time, love and species. Neuro. Endocrinol. Lett. 22:222–228.
   PubMed Web of Science ®Google Scholar
• Schaper SV, Dawson AS, Sharp PJ, Gienapp P, Caro SP, Visser ME. (2012). Increasing temperature, not mean temperature, is a cue for avian timing of reproduction. Am. Nat. 179:E55–E69.
   PubMed Web of Science ®Google Scholar
• Shimizu T, Masaki S. (1997). Geographical and species variation in circadian rhythm parameters in nemobiine crickets. Physiol. Entomol. 22:83–93.
   Web of Science ®Google Scholar
• Sibly R. (1975). How incentive and deficit determine feeding tendency. Anim. Behav. 23(Part 2):437–446.
   Google Scholar
• Spoelstra K. (2010). ChronoShop 1.01. http://www.hutlab.nl/ Accessed 10 October 2011.
   Google Scholar
• Strang-Karlsson S, Kajantie E, Pesonen A-K, Räikkönen K, Hovi P, Lahti J, Heinonen K, Järvenpää A-L, Eriksson JG, Andersson S, Paavonen J. (2010). Morningness propensity in young adults born prematurely: the Helsinki study of very low birth weight adults. Chronobiol. Int. 27:1829–1842.
   PubMed Web of Science ®Google Scholar
• Sweeney BM, Hastings JW. (1960). Effects of temperature upon diurnal rhythms. Cold Spring Harbor Symp. Quant. Biol. 25:87–104.
   PubMedGoogle Scholar
• Thomas RJ, Székely T, Cuthill IC, Harper DG, Newson SE, Frayling TD, Wallis PD. (2002). Eye size in birds and the timing of song at dawn. Proc. Biol. Sci. 269:831–837.
   PubMed Web of Science ®Google Scholar
• Vivanco P, Rol MÁ, Madrid JA. (2010). Temperature cycles trigger nocturnalism in the diurnal homeotherm Octodon degus. Chronobiol. Int. 27:517–534.
   PubMed Web of Science ®Google Scholar
• Wyse CA, Coogan AN, Selman C, Hazlerigg DG, Speakman JR. (2010). Association between mammalian lifespan and circadian free-running period: the circadian resonance hypothesis revisited. Biol. Lett. 6:696–698.
   PubMed Web of Science ®Google Scholar
• Ydenberg RC. (1984). The conflict between feeding and territorial defence in the great tit. Behav. Ecol. Sociobiol. 15:103–108.
   Web of Science ®Google Scholar