||This article needs more medical references for verification or relies too heavily on primary sources. (November 2013)|
A circadian rhythm // is any biological process that displays an endogenous, entrainable oscillation of about 24 hours. These 24-hour rhythms are driven by a circadian clock, and they have been widely observed in plants, animals, fungi, and cyanobacteria.
The term circadian comes from the Latin circa, meaning "around" (or "approximately"), and diēs, meaning "day". The formal study of biological temporal rhythms, such as daily, tidal, weekly, seasonal, and annual rhythms, is called chronobiology.
Although circadian rhythms are endogenous ("built-in", self-sustained), they are adjusted (entrained) to the local environment by external cues called zeitgebers (from German, "time giver"), which include light, temperature and redox cycles.
- 1 History
- 2 Criteria
- 3 Origin
- 4 Importance in animals
- 5 In plants
- 6 Biological clock in mammals
- 7 Light and the biological clock
- 8 Enforced longer cycles
- 9 Human health
- 10 See also
- 11 References
- 12 Further reading
- 13 External links
The earliest recorded account of a circadian process dates from the 4th century B.C.E., when Androsthenes, a ship captain serving under Alexander the Great, described diurnal leaf movements of the tamarind tree. The observation of a circadian or diurnal process in humans is mentioned in Chinese medical texts dated to around the 13th century, including the Noon and Midnight Manual and the Mnemonic Rhyme to Aid in the Selection of Acu-points According to the Diurnal Cycle, the Day of the Month and the Season of the Year.
The first recorded observation of an endogenous circadian oscillation was by the French scientist Jean-Jacques d'Ortous de Mairan in 1729. He noted that 24-hour patterns in the movement of the leaves of the plant Mimosa pudica continued even when the plants were kept in constant darkness, in the first experiment to attempt to distinguish an endogenous clock from responses to daily stimuli.
In 1896, Patrick and Gilbert observed that during a prolonged period of sleep deprivation, sleepiness increases and decreases with a period of approximately 24 hours. In 1918, J.S. Szymanski showed that animals are capable of maintaining 24-hour activity patterns in the absence of external cues such as light and changes in temperature. In the early 20th century, circadian rhythms were noticed in the rhythmic feeding times of bees. Extensive experiments were done by Auguste Forel, Ingeborg Beling, and Oskar Wahl to see whether this rhythm was due to an endogenous clock. Ron Konopka and Seymour Benzer isolated the first clock mutant in Drosophila in the early 1970s and mapped the "period" gene, the first discovered genetic determinant of behavioral rhythmicity. Joseph Takahashi discovered the first mammalian circadian clock mutation (clockΔ19) using mice in 1994. However, recent studies show that deletion of clock does not lead to a behavioral phenotype (the animals still have normal circadian rhythms), which questions its importance in rhythm generation.
To be called circadian, a biological rhythm must meet these three general criteria:
- The rhythm has an endogenous free-running period that lasts approximately 24 hours. The rhythm persists in constant conditions, (i.e., constant darkness) with a period of about 24 hours. The period of the rhythm in constant conditions is called the free-running period and is denoted by the Greek letter τ (tau). The rationale for this criterion is to distinguish circadian rhythms from simple responses to daily external cues. A rhythm cannot be said to be endogenous unless it has been tested and persists in conditions without external periodic input. In diurnal animals (active during daylight hours), in general τ is slightly greater than 24 hours, whereas, in nocturnal animals (active at night), in general τ is shorter than 24 hours.
- The rhythms are entrainable. The rhythm can be reset by exposure to external stimuli (such as light and heat), a process called entrainment. The external stimulus used to entrain a rhythm is called the Zeitgeber, or "time giver". Travel across time zones illustrates the ability of the human biological clock to adjust to the local time; a person will usually experience jet lag before entrainment of his/her circadian clock has brought it into sync with local time.
- The rhythms exhibit temperature compensation. In other words, they maintain circadian periodicity over a range of physiological temperatures. Many organisms live at a broad range of temperatures, and differences in thermal energy will affect the kinetics of all molecular processes in their cell(s). In order to keep track of time, the organism's circadian clock must maintain roughly a 24-hour periodicity despite the changing kinetics, a property known as temperature compensation. The Q10 Temperature Coefficient is a measure of this compensating effect. If the Q10 coefficient remains approximately 1 as temperature increases, the rhythm is considered to be temperature-compensated.
Circadian rhythms allow organisms to anticipate and prepare for precise and regular environmental changes. They thus enable organisms to best capitalize on environmental resources (e.g. light and food) compared to those that cannot predict such availability. It has therefore been suggested that circadian rhythms put organisms at a selective advantage in evolutionary terms. However, rhythmicity appears to be as important in regulating and coordinating internal metabolic processes, as in coordinating with the environment. This is suggested by the maintenance (heritability) of circadian rhythms in fruit flies after several hundred generations in constant laboratory conditions, as well as in creatures in constant darkness in the wild, and by the experimental elimination of behavioral, but not physiological, circadian rhythms in quail.
What drove circadian rhythms to evolve has been an enigmatic question. Previous hypotheses emphasized that photosensitive proteins and circadian rhythms may have originated together in the earliest cells, with the purpose of protecting replicating DNA from high levels of damaging ultraviolet radiation during the daytime. As a result, replication was relegated to the dark. However, evidence for this is lacking, since the simplest organisms with a circadian rhythm, the cyanobacteria, do the opposite of this - they divide more in the daytime. Recent studies instead highlight the importance of co-evolution of redox proteins with circadian oscillators in all three kingdoms of life following the Great Oxidation Event approx. 2.3 billion years ago. The current view is that circadian changes in environmental oxygen levels and the production of reactive oxygen species (ROS) in the presence of daylight are likely to have driven a need to evolve circadian rhythms to preempt, and therefore counteract, damaging redox reactions on a daily basis.
The simplest known circadian clock is that of the prokaryotic cyanobacteria. Recent research has demonstrated that the circadian clock of Synechococcus elongatus can be reconstituted in vitro with just the three proteins (KaiA, KaiB, KaiC) of their central oscillator. This clock has been shown to sustain a 22-hour rhythm over several days upon the addition of ATP. Previous explanations of the prokaryotic circadian timekeeper were dependent upon a DNA transcription/translation feedback mechanism.
A defect in the human homologue of the Drosophila "period" gene was identified as a cause of the sleep disorder FASPS (Familial advanced sleep phase syndrome), underscoring the conserved nature of the molecular circadian clock through evolution. Many more genetic components of the biological clock are now known. Their interactions result in an interlocked feedback loop of gene products resulting in periodic fluctuations that the cells of the body interpret as a specific time of the day.
It is now known that the molecular circadian clock can function within a single cell; i.e., it is cell-autonomous. This was shown by Gene Block in isolated mollusk BRNs.[clarification needed] At the same time, different cells may communicate with each other resulting in a synchronised output of electrical signaling. These may interface with endocrine glands of the brain to result in periodic release of hormones. The receptors for these hormones may be located far across the body and synchronise the peripheral clocks of various organs. Thus, the information of the time of the day as relayed by the eyes travels to the clock in the brain, and, through that, clocks in the rest of the body may be synchronised. This is how the timing of, for example, sleep/wake, body temperature, thirst, and appetite are coordinately controlled by the biological clock.
Importance in animals
Circadian rhythmicity is present in the sleeping and feeding patterns of animals, including human beings. There are also clear patterns of core body temperature, brain wave activity, hormone production, cell regeneration, and other biological activities. In addition, photoperiodism, the physiological reaction of organisms to the length of day or night, is vital to both plants and animals, and the circadian system plays a role in the measurement and interpretation of day length.
|“||Timely prediction of seasonal periods of weather conditions, food availability, or predator activity is crucial for survival of many species. Although not the only parameter, the changing length of the photoperiod ('daylength') is the most predictive environmental cue for the seasonal timing of physiology and behavior, most notably for timing of migration, hibernation, and reproduction.||”|
Impact of circadian disruption
||This section possibly contains original research. (December 2013)|
Mutations or deletions of clock gene in mice have demonstrated the importance of body clocks to ensure the proper timing of cellular/metabolic events; clock-mutant mice are hyperphagic and obese, and have altered glucose metabolism. In mice, deletion of the Rev-ErbA alpha clock gene facilitates diet-induced obesity and changes the balance between glucose and lipid utilization predisposing to diabetes. However, it is not clear whether there is a strong association between clock gene polymorphisms in humans and the susceptibility to develop the metabolic syndrome.
Impact of light–dark cycle
The rhythm is linked to the light–dark cycle. Animals, including humans, kept in total darkness for extended periods eventually function with a free-running rhythm. Their sleep cycle is pushed back or forward each "day", depending on whether their "day", their endogenous period, is shorter or longer than 24 hours. The environmental cues that reset the rhythms each day are called zeitgebers (from the German, "time-givers"). Totally blind subterranean mammals (e.g., blind mole rat Spalax sp.) are able to maintain their endogenous clocks in the apparent absence of external stimuli. Although they lack image-forming eyes, their photoreceptors (which detect light) are still functional; they do surface periodically as well.[page needed]
Free-running organisms that normally have one or two consolidated sleep episodes will still have them when in an environment shielded from external cues, but the rhythm is, of course, not entrained to the 24-hour light–dark cycle in nature. The sleep–wake rhythm may, in these circumstances, become out of phase with other circadian or ultradian rhythms such as metabolic, hormonal, CNS electrical, or neurotransmitter rhythms.
Norwegian researchers at the University of Tromsø have shown that some Arctic animals (ptarmigan, reindeer) show circadian rhythms only in the parts of the year that have daily sunrises and sunsets. In one study of reindeer, animals at 70 degrees North showed circadian rhythms in the autumn, winter and spring, but not in the summer. Reindeer on Svalbard at 78 degrees North showed such rhythms only in autumn and spring. The researchers suspect that other Arctic animals as well may not show circadian rhythms in the constant light of summer and the constant dark of winter.
A 2006 study in northern Alaska found that day-living ground squirrels and nocturnal porcupines strictly maintain their circadian rhythms through 82 days and nights of sunshine. The researchers speculate that these two rodents notice that the apparent distance between the sun and the horizon is shortest once a day, and, thus, a sufficient signal to entrain (adjust) by.
The navigation of the fall migration of the Eastern North American monarch butterfly (Danaus plexippus) to their overwintering grounds in central Mexico uses a time-compensated sun compass that depends upon a circadian clock in their antennae.
Plant circadian rhythms tell the plant what season it is and when to flower for the best chance of attracting pollinators. Behaviors showing rhythms include leaf movement, growth, germination, stomatal/gas exchange, enzyme activity, photosynthetic activity, and fragrance emission, among others. Circadian rhythms occur as a plant entrains to synchronize with the light cycle of its surrounding environment. These rhythms are endogenously generated and self-sustaining and are relatively constant over a range of ambient temperatures. Important features include two interacting transcription-translation feedback loops: proteins containing PAS domains, which facilitate protein-protein interactions; and several photoreceptors that fine-tune the clock to different light conditions. Anticipation of changes in the environment allows appropriate changes in a plant's physiological state, conferring an adaptive advantage. A better understanding of plant circadian rhythms has applications in agriculture, such as helping farmers stagger crop harvests to extend crop availability and securing against massive losses due to weather.
Light is the signal by which plants synchronize their internal clocks to their environment and is sensed by a wide variety of photoreceptors. Red and blue light are absorbed through several phytochromes and cryptochromes. One phytochrome, phyA, is the main phytochrome in seedlings grown in the dark but rapidly degrades in light to produce Cry1. Phytochromes B–E are more stable with phyB, the main phytochrome in seedlings grown in the light. The cryptochrome (cry) gene is also a light-sensitive component of the circadian clock and is thought to be involved both as a photoreceptor and as part of the clock's endogenous pacemaker mechanism. Cryptochromes 1–2 (involved in blue–UVA) help to maintain the period length in the clock through a whole range of light conditions.
The central oscillator generates a self-sustaining rhythm and is driven by two interacting feedback loops that are active at different times of day. The morning loop consists of CCA1 (Circadian and Clock-Associated 1) and LHY (Late Elongated Hypocotyl), which encode closely related MYB transcription factors that regulate circadian rhythms in Arabidopsis, as well as PRR 7 and 9 (Pseudo-Response Regulators.) The evening loop consists of GI (Gigantea) and ELF4, both involved in regulation of flowering time genes. When CCA1 and LHY are overexpressed (under constant light or dark conditions), plants become arrhythmic, and mRNA signals reduce, contributing to a negative feedback loop. Gene expression of CCA1 and LHY oscillates and peaks in the early morning, whereas TOC1 gene expression oscillates and peaks in the early evening. While it was previously hypothesised that these three genes model a negative feedback loop in which over-expressed CCA1 and LHY repress TOC1 and over-expressed TOC1 is a positive regulator of CCA1 and LHY, it was shown in 2012 by Andrew Millar and others that TOC1 in fact serves as a repressor not only of CCA1, LHY, and PRR7 and 9 in the morning loop but also of GI and ELF4 in the evening loop. This finding and further computational modeling of TOC1 gene functions and interactions suggest a reframing of the plant circadian clock as a triple negative-component repressilator model rather than the positive/negative-element feedback loop characterizing the clock in mammals.
Biological clock in mammals
The primary circadian "clock" in mammals is located in the suprachiasmatic nucleus (or nuclei) (SCN), a pair of distinct groups of cells located in the hypothalamus. Destruction of the SCN results in the complete absence of a regular sleep–wake rhythm. The SCN receives information about illumination through the eyes. The retina of the eye contains "classical" photoreceptors ("rods" and "cones"), which are used for conventional vision. But the retina also contains specialized ganglion cells that are directly photosensitive, and project directly to the SCN, where they help in the entrainment (synchronization) of this master circadian clock.
These cells contain the photopigment melanopsin and their signals follow a pathway called the retinohypothalamic tract, leading to the SCN. If cells from the SCN are removed and cultured, they maintain their own rhythm in the absence of external cues.
The SCN takes the information on the lengths of the day and night from the retina, interprets it, and passes it on to the pineal gland, a tiny structure shaped like a pine cone and located on the epithalamus. In response, the pineal secretes the hormone melatonin. Secretion of melatonin peaks at night and ebbs during the day and its presence provides information about night-length.
Several studies have indicated that pineal melatonin feeds back on SCN rhythmicity to modulate circadian patterns of activity and other processes. However, the nature and system-level significance of this feedback are unknown.
The circadian rhythms of humans can be entrained to slightly shorter and longer periods than the Earth's 24 hours. Researchers at Harvard have shown that human subjects can at least be entrained to a 23.5-hour cycle and a 24.65-hour cycle (the latter being the natural solar day-night cycle on the planet Mars).
Early research into circadian rhythms suggested that most people preferred a day closer to 25 hours when isolated from external stimuli like daylight and timekeeping. However, this research was faulty because it failed to shield the participants from artificial light. Although subjects were shielded from time cues (like clocks) and daylight, the researchers were not aware of the phase-delaying effects of indoor electric lights.[dubious ] The subjects were allowed to turn on light when they were awake and to turn it off when they wanted to sleep. Electric light in the evening delayed their circadian phase.
Biological markers and effects
The classic phase markers for measuring the timing of a mammal's circadian rhythm are:
- melatonin secretion by the pineal gland,
- core body temperature minimum, and
- plasma level of cortisol.
For temperature studies, subjects must remain awake but calm and semi-reclined in near darkness while their rectal temperatures are taken continuously. Though variation is great among normal chronotypes, the average human adult's temperature reaches its minimum at about 05:00 (5 a.m.), about two hours before habitual wake time. Baehr et al. found that, in young adults, the daily body temperature minimum occurred at about 04:00 (4 a.m.) for morning types but at about 06:00 (6 a.m.) for evening types. This minimum occurred at approximately the middle of the eight hour sleep period for morning types, but closer to waking in evening types.
Melatonin is absent from the system or undetectably low during daytime. Its onset in dim light, dim-light melatonin onset (DLMO), at roughly 21:00 (9 p.m.) can be measured in the blood or the saliva. Its major metabolite can also be measured in morning urine. Both DLMO and the midpoint (in time) of the presence of the hormone in the blood or saliva have been used as circadian markers. However, newer research indicates that the melatonin offset may be the more reliable marker. Benloucif et al. found that melatonin phase markers were more stable and more highly correlated with the timing of sleep than the core temperature minimum. They found that both sleep offset and melatonin offset are more strongly correlated with phase markers than the onset of sleep. In addition, the declining phase of the melatonin levels is more reliable and stable than the termination of melatonin synthesis.
Other physiological changes that occur according to a circadian rhythm include heart rate and many cellular processes "including oxidative stress, cell metabolism, immune and inflammatory responses, epigenetic modification, hypoxia/hyperoxia response pathways, endoplasmic reticular stress, autophagy, and regulation of the stem cell environment."
In contradiction to previous studies, it has been found that there is no effect of body temperature on performance on psychological tests. This is likely due to evolutionary pressures for higher cognitive function compared to the other areas of function examined in previous studies.
Outside the "master clock"
More-or-less independent circadian rhythms are found in many organs and cells in the body outside the suprachiasmatic nuclei (SCN), the "master clock". These clocks, called peripheral oscillators, are found in the adrenal gland, oesophagus, lungs, liver, pancreas, spleen, thymus, and skin. Though oscillators in the skin respond to light, a systemic influence has not been proven. There is also some evidence that the olfactory bulb and prostate may experience oscillations when cultured, suggesting that these structures may also be weak oscillators.
Furthermore, liver cells, for example, appear to respond to feeding rather than to light. Cells from many parts of the body appear to have free-running rhythms.
Light and the biological clock
Light resets the biological clock in accordance with the phase response curve (PRC). Depending on the timing, light can advance or delay the circadian rhythm. Both the PRC and the required illuminance vary from species to species and lower light levels are required to reset the clocks in nocturnal rodents than in humans.
Enforced longer cycles
Studies by Nathaniel Kleitman in 1938 and by Derk-Jan Dijk and Charles Czeisler in the 1990s put human subjects on enforced 28-hour sleep–wake cycles, in constant dim light and with other time cues suppressed, for over a month. Because normal people cannot entrain to a 28-hour day in dim light if at all, this is referred to as a forced desynchrony protocol. Sleep and wake episodes are uncoupled from the endogenous circadian period of about 24.18 hours and researchers are allowed to assess the effects of circadian phase on aspects of sleep and wakefulness including sleep latency and other functions.[page needed]
Timing of medical treatment in coordination with the body clock may significantly increase efficacy and reduce drug toxicity or adverse reactions.
A number of studies have concluded that a short period of sleep during the day, a power-nap, does not have any measurable effect on normal circadian rhythms but can decrease stress and improve productivity.[medical citation needed]
Health problems can result from a disturbance to the circadian rhythm. Circadian rhythms also play a part in the reticular activating system, which is crucial for maintaining a state of consciousness. A reversal in the sleep–wake cycle may be a sign or complication of uremia, azotemia or acute renal failure.[medical citation needed]
Studies have also shown that light has a direct effect on human health because of the way it influences the circadian rhythms.
Obesity and diabetes
Obesity and diabetes are associated with lifestyle and genetic factors. Among those factors, disruption of the circadian clockwork and/or misalignment of the circadian timing system with the external environment (e.g., light-dark cycle) might play a role in the development of metabolic disorders.
Shift-work or chronic jet-lag have profound consequences on circadian and metabolic events in the body. Animals that are forced to eat during their resting period show increased body mass and altered expression of clock and metabolic genes.[medical citation needed] In humans, shift-work that favors irregular eating times is associated with altered insulin sensitivity and higher body mass. Shift-work also leads to increased metabolic risks for cardio-metabolic syndrome, hypertension, inflammation.
Due to the work nature of airline pilots, who often cross several timezones and regions of sunlight and darkness in one day, and spend many hours awake both day and night, they are often unable to maintain sleep patterns that correspond to the natural human circadian rhythm; this situation can easily lead to fatigue. The NTSB cites this as contributing to many accidents[unreliable medical source?]  and has conducted several research studies in order to find methods of combating fatigue in pilots.
Disruption to rhythms usually has a negative effect. Many travellers have experienced the condition known as jet lag, with its associated symptoms of fatigue, disorientation, and insomnia.[medical citation needed]
A number of other disorders, for example bipolar disorder and some sleep disorders such as delayed sleep phase disorder (DSPD), are associated with irregular or pathological functioning of circadian rhythms.[medical citation needed]
Disruption to rhythms in the longer term is believed to have significant adverse health consequences on peripheral organs outside the brain, in particular in the development or exacerbation of cardiovascular disease. LED lighting suppresses melatonin production five times more than a high-pressure sodium light.[medical citation needed] Depression symptoms from long term nighttime light exposure can be undone by returning to a normal cycle.[medical citation needed]
Effect of drugs
Studies conducted on both animals and humans show major bidirectional relationships between the circadian system and abusive drugs. It is indicated that these abusive drugs affect the central circadian pacemaker. Individuals suffering from substance abuse display disrupted rhythms. These disrupted rhythms can increase the risk for substance abuse and relapse. It is possible that genetic and/or environmental disturbances to the normal sleep and wake cycle can increase the susceptibility to addiction.
It is difficult to determine if a disturbance in the circadian rhythm is at fault for an increase in prevalence for substance abuse or if other environmental factors such as stress are to blame. Changes to the circadian rhythm and sleep occur once an individual begins abusing drugs and alcohol. Once an individual chooses to stop using drugs and alcohol, the circadian rhythm continues to be disrupted.
The stabilization of sleep and the circadian rhythm might possibly help to reduce the vulnerability to addiction and reduce the chances of relapse.
Circadian rhythms and clock genes expressed in brain regions outside the suprachiasmatic nucleus may significantly influence the effects produced by drugs such as cocaine. Moreover, genetic manipulations of clock genes profoundly affect cocaine's actions.
- Edgar, Rachel S.; Green, Edward W.; Zhao, Yuwei; van Ooijen, Gerben; Olmedo, Maria; Qin, Ximing; Xu, Yao; Pan, Min; Valekunja, Utham K. (May 24, 2012). "Peroxiredoxins are conserved markers of circadian rhythms". Nature 485 (7399): 459–464. doi:10.1038/nature11088. ISSN 0028-0836. PMC 3398137. PMID 22622569.
- Bass, Joseph (November 15, 2012). "Circadian topology of metabolism". Nature 491 (7424): 348–356. doi:10.1038/nature11704. ISSN 0028-0836.
- Bretzl H (1903). Botanische Forschungen des Alexanderzuges. Leipzig: Teubner.[page needed]
- Gwei-Djen Lu (25 October 2002). Celestial Lancets. Psychology Press. pp. 137–140. ISBN 978-0-7007-1458-2.
- de Mairan JJO (1729). "Observation Botanique". Histoire de l'Academie Royale des Sciences: 35–36.
- Gardner MJ, Hubbard KE, Hotta CT, Dodd AN, Webb AA; Hubbard; Hotta; Dodd; Webb (July 2006). "How plants tell the time". Biochem. J. 397 (1): 15–24. doi:10.1042/BJ20060484. PMC 1479754. PMID 16761955.
- Dijk DJ, von Schantz M; von Schantz (August 2005). "Timing and consolidation of human sleep, wakefulness, and performance by a symphony of oscillators". J. Biol. Rhythms 20 (4): 279–90. doi:10.1177/0748730405278292. PMID 16077148.
- Danchin A. "Important dates 1900–1919". HKU-Pasteur Research Centre (Paris). Retrieved 2008-01-12.
- Konopka RJ, Benzer S; Benzer (September 1971). "Clock mutants of Drosophila melanogaster". Proc. Natl. Acad. Sci. U.S.A. 68 (9): 2112–6. Bibcode:1971PNAS...68.2112K. doi:10.1073/pnas.68.9.2112. PMC 389363. PMID 5002428.
- [unreliable medical source?] "Gene Discovered in Mice that Regulates Biological Clock". Chicago Tribune. 29 April 1994.
- [non-primary source needed] Vitaterna MH, King DP, Chang AM et al. (April 1994). "Mutagenesis and mapping of a mouse gene, Clock, essential for circadian behavior". Science 264 (5159): 719–25. doi:10.1126/science.8171325. PMID 8171325.
- DeBruyne (2006). "A Clock Shock: Mouse CLOCK Is Not Required for Circadian Oscillator Function". Neuron. doi:10.1016/j.neuron.2006.03.041. PMID 16675400.
- Collins, Ben (2006). "Keeping time without a clock". Neuron. doi:10.1016/j.neuron.2006.03.041. PMID 16675389.
- Halberg F, Cornélissen G, Katinas G et al. (October 2003). "Transdisciplinary unifying implications of circadian findings in the 1950s". J Circadian Rhythms 1 (1): 2. doi:10.1186/1740-3391-1-2. PMC 317388. PMID 14728726.
Eventually I reverted, for the same reason, to "circadian" ...
- Johnson, Carl (2004). Chronobiology: Biological Timekeeping. Sunderland, Massachusetts, USA: Sinauer Associates, Inc. pp. 67–105.
- Sharma VK (November 2003). "Adaptive significance of circadian clocks". Chronobiology International 20 (6): 901–19. doi:10.1081/CBI-120026099. PMID 14680135.
- [non-primary source needed] Sheeba V, Sharma VK, Chandrashekaran MK, Joshi A; Sharma; Chandrashekaran; Joshi (September 1999). "Persistence of eclosion rhythm in Drosophila melanogaster after 600 generations in an aperiodic environment". Naturwissenschaften 86 (9): 448–9. Bibcode:1999NW.....86..448S. doi:10.1007/s001140050651. PMID 10501695.
- [non-primary source needed] Guyomarc'h C, Lumineau S, Richard JP; Lumineau; Richard (May 1998). "Circadian rhythm of activity in Japanese quail in constant darkness: variability of clarity and possibility of selection". Chronobiol. Int. 15 (3): 219–30. doi:10.3109/07420529808998685. PMID 9653576.
- [non-primary source needed] Zivkovic BD, Underwood H, Steele CT, Edmonds K; Underwood; Steele; Edmonds (October 1999). "Formal properties of the circadian and photoperiodic systems of Japanese quail: phase response curve and effects of T-cycles". J. Biol. Rhythms 14 (5): 378–90. doi:10.1177/074873099129000786. PMID 10511005.
- Mori, Tetsuya; Johnson, Carl Hirschie (2001-04-15). "Independence of Circadian Timing from Cell Division in Cyanobacteria". Journal of Bacteriology 183 (8): 2439–2444. doi:10.1128/JB.183.8.2439-2444.2001. ISSN 0021-9193. PMID 11274102.
- Hut RA, Beersma DG; Beersma (July 2011). "Evolution of time-keeping mechanisms: early emergence and adaptation to photoperiod". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 366 (1574): 2141–54. doi:10.1098/rstb.2010.0409. PMC 3130368. PMID 21690131.
- [unreliable medical source?] Nagoshi E, Saini C, Bauer C, Laroche T, Naef F, Schibler U; Saini; Bauer; Laroche; Naef; Schibler (November 2004). "Circadian gene expression in individual fibroblasts: cell-autonomous and self-sustained oscillators pass time to daughter cells". Cell 119 (5): 693–705. doi:10.1016/j.cell.2004.11.015. PMID 15550250.
- [non-primary source needed] Michel S, Geusz ME, Zaritsky JJ, Block GD; Geusz; Zaritsky; Block (January 1993). "Circadian rhythm in membrane conductance expressed in isolated neurons". Science 259 (5092): 239–41. doi:10.1126/science.8421785. PMID 8421785.
- [unreliable medical source?] Zivkovic, Bora "Coturnix" (2007-07-25). "Clock Tutorial #16: Photoperiodism – Models and Experimental Approaches (original work from 2005-08-13)". A Blog Around the Clock. ScienceBlogs. Retrieved 2007-12-09.
- [non-primary source needed] Turek FW, Joshu C, Kohsaka A et al. (May 2005). "Obesity and metabolic syndrome in circadian Clock mutant mice". Science 308 (5724): 1043–5. doi:10.1126/science.1108750. PMC 3764501. PMID 15845877.
- Delezie J, Dumont S, Dardente H et al. (August 2012). "The nuclear receptor REV-ERBα is required for the daily balance of carbohydrate and lipid metabolism". FASEB J. 26 (8): 3321–35. doi:10.1096/fj.12-208751. PMID 22562834.
- [non-primary source needed] Delezie J, Dumont S, Dardente H et al. (August 2012). "The nuclear receptor REV-ERBα is required for the daily balance of carbohydrate and lipid metabolism". FASEB J. 26 (8): 3321–35. doi:10.1096/fj.12-208751. PMID 22562834.
- [non-primary source needed] Scott EM, Carter AM, Grant PJ; Carter; Grant (2007). "Association between polymorphisms in the Clock gene, obesity and the metabolic syndrome in man". International Journal of Obesity 32 (4): 658–62. doi:10.1038/sj.ijo.0803778. PMID 18071340.
- [unreliable medical source?] Shneerson, J.M.; Ohayon, M.M.; Carskadon, M.A. (2007). "Circadian rhythms". Rapid eye movement (REM) sleep. Armenian Medical Network. Retrieved 2007-09-19.
- "The Rhythms of Life: The Biological Clocks That Control the Daily Lives of Every Living Thing" Russell Foster & Leon Kreitzman, Publisher: Profile Books Ltd.
- [unreliable medical source?] Regestein QR, Pavlova M; Pavlova (September 1995). "Treatment of delayed sleep phase syndrome". Gen Hosp Psychiatry 17 (5): 335–45. doi:10.1016/0163-8343(95)00062-V. PMID 8522148.
- [unreliable medical source?] Elizabeth Howell (14 December 2012). "Space Station to Get New Insomnia-Fighting Light Bulbs". Retrieved 2012-12-17.
- [non-primary source needed] Spilde, Ingrid (December 2005). "Reinsdyr uten døgnrytme" (in Norwegian and Bokmål). forskning.no. Retrieved 2007-11-24.
...så det ikke ut til at reinen hadde noen døgnrytme om sommeren. Svalbardreinen hadde det heller ikke om vinteren.
- Folk, G. Edgar; Thrift, Diana L.; Zimmerman, M. Bridget; Reimann, Paul (2006-12-01). "Mammalian activity – rest rhythms in Arctic continuous daylight". Biological Rhythm Research 37 (6): 455–469. doi:10.1080/09291010600738551. Retrieved 2014-09-21.
Would local animals maintained under natural continuous daylight demonstrate the Aschoff effect described in previously published laboratory experiments using continuous light, in which rats' circadian activity patterns changed systematically to a longer period, expressing a 26-hour day of activity and rest?
- [non-primary source needed] Merlin C, Gegear RJ, Reppert SM; Gegear; Reppert (September 2009). "Antennal circadian clocks coordinate sun compass orientation in migratory monarch butterflies". Science 325 (5948): 1700–4. Bibcode:2009Sci...325.1700M. doi:10.1126/science.1176221. PMC 2754321. PMID 19779201.
- [non-primary source needed] Kyriacou CP (September 2009). "Physiology. Unraveling traveling". Science 325 (5948): 1629–30. doi:10.1126/science.1178935. PMID 19779177.
- Webb AAR (June 2003). "The physiology of circadian rhythms in plants". New Phytologist 160 (160): 281–303. doi:10.1046/j.1469-8137.2003.00895.x. JSTOR 1514280.
- McClung CR (April 2006). "Plant circadian rhythms". Plant Cell 18 (4): 792–803. doi:10.1105/tpc.106.040980. PMC 1425852. PMID 16595397.
- Mizoguchi T, Wright L, Fujiwara S et al. (August 2005). "Distinct roles of GIGANTEA in promoting flowering and regulating circadian rhythms in Arabidopsis". Plant Cell 17 (8): 2255–70. doi:10.1105/tpc.105.033464. PMC 1182487. PMID 16006578.
- Kolmos E, Davis SJ; Davis (September 2007). "ELF4 as a Central Gene in the Circadian Clock". Plant Signal Behav 2 (5): 370–2. doi:10.4161/psb.2.5.4463. PMC 2634215. PMID 19704602.
- Pokhilko A, Fernández AP, Edwards KD, Southern MM, Halliday KJ, Millar AJ; Fernández; Edwards; Southern; Halliday; Millar (2012). "The clock gene circuit in Arabidopsis includes a repressilator with additional feedback loops". Mol. Syst. Biol. 8: 574. doi:10.1038/msb.2012.6. PMC 3321525. PMID 22395476.
- "Biological Clock in Mammals". BioInteractive. Howard Hughes Medical Institute. Retrieved 5 May 2015.
- Welsh, David K.; Takahashi, Joseph S.; Kay, Steve A. (March 2010). "Suprachiasmatic Nucleus: Cell Autonomy and Network Properties". Annu Rev Physiol. 72: 551–577. doi:10.1146/annurev-physiol-021909-135919. Retrieved 5 May 2015.
- [unreliable medical source?] Scheer FA, Wright KP, Kronauer RE, Czeisler CA; Wright Jr; Kronauer; Czeisler (2007). "Plasticity of the intrinsic period of the human circadian timing system". PLoS ONE 2 (8): e721. Bibcode:2007PLoSO...2..721S. doi:10.1371/journal.pone.0000721. PMC 1934931. PMID 17684566.
- [unreliable medical source?] Duffy JF, Wright KP; Wright Jr (August 2005). "Entrainment of the human circadian system by light". J. Biol. Rhythms 20 (4): 326–38. doi:10.1177/0748730405277983. PMID 16077152.
- Benloucif, S.; Guico, M. J.; Reid, K. J.; Wolfe, L. F.; l'Hermite-Balériaux, M; Zee, P. C. (2005). "Stability of Melatonin and Temperature as Circadian Phase Markers and Their Relation to Sleep Times in Humans". Journal of Biological Rhythms 20 (2): 178–188. doi:10.1177/0748730404273983. ISSN 0748-7304. PMID 15834114.
- Baehr, E.K.; Revelle, W.; Eastman, C.I. (June 2000). "Individual differences in the phase and amplitude of the human circadian temperature rhythm: with an emphasis on morningness-eveningness". J Sleep Res 9 (2): 117–27. doi:10.1046/j.1365-2869.2000.00196.x. PMID 10849238.
- "NHLBI Workshop: "Circadian Clock at the Interface of Lung Health and Disease" April 28-29, 2014 Executive Summary". National Heart, Lung, and Blood Institute. September 2014. Retrieved 20 September 2014.
- Quartel, Lara (2014). "The effect of the circadian rhythm of body temperature on A-level exam performance". Undergraduate Journal of Psychology 27 (1).
- Kawara S, Mydlarski R, Mamelak AJ et al. (December 2002). "Low-dose ultraviolet B rays alter the mRNA expression of the circadian clock genes in cultured human keratinocytes". J. Invest. Dermatol. 119 (6): 1220–3. doi:10.1046/j.1523-1747.2002.19619.x. PMID 12485420.
- Aldrich, Michael S. (1999). Sleep medicine. New York: Oxford University Press. ISBN 0-19-512957-1.
- Grote L, Mayer J, Penzel T et al. (1994). "Nocturnal hypertension and cardiovascular risk: consequences for diagnosis and treatment". J. Cardiovasc. Pharmacol. 24 Suppl 2: S26–38. PMID 7898092.
- Zelinski, EL (2014). "The trouble with circadian clock dysfunction: Multiple deleterious effects on the brain and body.". Neuroscience and Biobehavioral Reviews (40): 80–101. doi:10.1016/j.neubiorev.2014.01.007. PMID 24468109. Retrieved 12 April 2015.
- Sinert T, Peacock PR (10 May 2006). "Renal Failure, Acute". eMedicine from WebMD. Retrieved 2008-08-03.
- Figueiro MG, Rea MS, Bullough JD (2006). "Does architectural lighting contribute to breast cancer?". J Carcinog 5: 20. doi:10.1186/1477-3163-5-20. PMC 1557490. PMID 16901343.
- Delezie J, Challet E (December 2011). "Interactions between metabolism and circadian clocks: reciprocal disturbances". Ann. N. Y. Acad. Sci. 1243: 30–46. doi:10.1111/j.1749-6632.2011.06246.x. PMID 22211891.
- [unreliable medical source?] http://www.aviationweek.com/aw/jsp_includes/articlePrint.jsp?storyID=news/FATIGex.xml&headLine=null Aviation Week Article[full citation needed]
- http://aeromedical.org/Articles/Pilot_Fatigue.html Pilot Fatigue Study[full citation needed]
- http://www.cnn.com/2009/TRAVEL/05/15/pilot.fatigue.buffalo.crash/index.html CNN Article[full citation needed]
- Oritz-Tuldela E, Martinez-Nicolas A, Diaz-Mardomingo C, Garcia-Herranz S, Pereda-Perez I, Valencia A, Peraita H, Venero C, Madrid J, Rol M. 2014. The Characterization of Biological Rhythms in Mild Cognitive Impairment. BioMed Research International.
- Aschoff, J. (ed.) (1965) Circadian Clocks. North Holland Press, Amsterdam
- Avivi, A.; Albrecht, U.; Oster, H.; Joel, A.; Beiles, A.; Nevo, E. (November 2001). "Biological clock in total darkness: the Clock/MOP3 circadian system of the blind subterranean mole rat". Proceedings of the National Academy of Sciences of the United States of America 98 (24): 13751–6. Bibcode:2001PNAS...9813751A. doi:10.1073/pnas.181484498. PMC 61113. PMID 11707566.
- Avivi, A.; Oster, H.; Joel, A.; Beiles, A.; Albrecht, U.; Nevo, E. (September 2002). "Circadian genes in a blind subterranean mammal II: conservation and uniqueness of the three Period homologs in the blind subterranean mole rat, Spalax ehrenbergi superspecies". Proceedings of the National Academy of Sciences of the United States of America 99 (18): 11718–23. Bibcode:2002PNAS...9911718A. doi:10.1073/pnas.182423299. PMC 129335. PMID 12193657.
- Ditty, J.L.; Williams, S.B.; Golden, S.S. (2003). "A cyanobacterial circadian timing mechanism". Annual Review of Genetics 37: 513–43. doi:10.1146/annurev.genet.37.110801.142716. PMID 14616072.
- Dunlap, J.C.; Loros, J.; DeCoursey, P.J. (2003) Chronobiology: Biological Timekeeping. Sinauer, Sunderland
- Dvornyk, V.; Vinogradova, O.; Nevo, E. (March 2003). "Origin and evolution of circadian clock genes in prokaryotes". Proceedings of the National Academy of Sciences of the United States of America 100 (5): 2495–500. Bibcode:2003PNAS..100.2495D. doi:10.1073/pnas.0130099100. PMC 151369. PMID 12604787.
- Koukkari, W.L.; Sothern, R.B. (2006) Introducing Biological Rhythms. Springer, New York
- Martino, T.; Arab, S.; Straume, M.; Belsham, Denise D. et al. (April 2004). "Day/night rhythms in gene expression of the normal murine heart". Journal of Molecular Medicine 82 (4): 256–64. doi:10.1007/s00109-003-0520-1. PMID 14985853.
- Refinetti, R. (2006) Circadian Physiology, 2nd ed. CRC Press, Boca Raton
- Takahashi, J.S.; Zatz, M. (September 1982). "Regulation of circadian rhythmicity". Science 217 (4565): 1104–11. Bibcode:1982Sci...217.1104T. doi:10.1126/science.6287576. PMID 6287576.
- Tomita, J.; Nakajima, M.; Kondo, T.; Iwasaki, H. (January 2005). "No transcription-translation feedback in circadian rhythm of KaiC phosphorylation". Science 307 (5707): 251–4. Bibcode:2005Sci...307..251T. doi:10.1126/science.1102540. PMID 15550625.
- Moore-Ede, Martin C.; Sulzman, Frank M.; Fuller, Charles A. (1982). The Clocks that Time Us: Physiology of the Circadian Timing System. Cambridge, Massachusetts: Harvard University Press. ISBN 0-674-13581-4.
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