Zoovet Travel · Technical Series VII — Chronobiology and transport stress February 2026
Technical review: chronobiology, HPA/SAM axes, zeitgebers

Circadian desynchronization and transport stress in dogs and cats: the phenomenon commonly known as «jet lag»

Rigorous review of the available scientific basis on canine and feline chronobiology, physiological impact of transport, and plausibility of a post-flight circadian desynchronization syndrome in these species, distinguishing direct evidence from well-founded biological inferences.

Jessica Ysabel Camacho Garcia, DVM — CMVP 12434  |  Víctor Jesús Camacho Paz, DVM — CMVP 3103 — Zoovet Travel, Lima, Peru  |  Review: February 2026
Scope and limitations of this document Species: Dog (Canis lupus familiaris) and cat (Felis catus). The term «jet lag» is used in this article as an operational label for a clinically heterogeneous phenomenon: the combination of circadian desynchronization and acute/chronic transport stress. It does not imply that human jet lag is directly extrapolable to these species. Where evidence comes from studies in humans or rodents, this is explicitly stated. Biological inferences based on conserved mechanisms are presented as plausible hypotheses, not as proven facts in dog/cat. This document is informative and for technical reference. It does not constitute veterinary prescription or clinical guidance. Any management decision must be made by a treating veterinarian.
Structured abstract Context: International transport of companion animals across multiple time zones exposes dogs and cats to two simultaneous physiological perturbations: acute travel stress, mediated by the Sympathetic-Adreno-Medullary (SAM) and Hypothalamic-Pituitary-Adrenal (HPA) axes, and desynchronization of the zeitgebers (temporal synchronizers) that regulate the animal's circadian rhythms. The confluence of both mechanisms produces a picture of behavioural, sleep, appetite and gastrointestinal alterations colloquially referred to as «jet lag» in veterinary clinical practice and in the pet relocation industry.

Objective: To rigorously review the available scientific basis on canine and feline chronobiology, the physiological impact of transport, and the plausibility of a post-flight circadian desynchronization syndrome in these species, distinguishing direct evidence from well-founded biological inferences.

Methods: Review of peer-reviewed primary sources including: Wenchner et al. (2024, Scientific Reports), Leadbeater et al. (2021, Veterinary Record), Bognár et al. (2021, Animals), Wormald et al. (2017, Applied Animal Behaviour Science), Piccione et al. (2013, JFMS), Pastore et al. (2011, Animal Welfare), Kis et al. (2014, Proc. Biol. Sci.), Andrews et al. (2015, JFMS), Beerda et al. (1998, Physiology & Behavior), Zanghi (2016, Journal of Veterinary Behavior), Randall et al. (1985, Reviews in Veterinary Science) and Dunlap et al. (2015, AJVR).

Main findings: (1) There is direct evidence in dogs of rhythm desynchronization due to changes in human cohabitation schedules (social jetlag, Wenchner 2024). (2) Air transport induces documented activation of the SAM and HPA axes in dogs, with elevated cortisol for up to 48 hours post-travel (Leadbeater 2021). (3) Dogs have a measurable chronotype with actigraphy and their sleep-wake rhythm is sensitive to environmental perturbations (Bognár 2021). (4) Cats are fundamentally crepuscular with a well-documented circadian body temperature rhythm, highly dependent on the light/dark cycle (Piccione 2013, Randall 1985). (5) There are no actigraphy studies conducted during flight nor clinical trials on post-flight resynchronization in either species.

Limitations: The absence of longitudinal actigraphy studies pre/post transmeridian flight in dogs and cats requires building the article's theoretical model on inferences from conserved biological mechanisms. This limitation is explicitly stated in each section where it applies.

Keywords: veterinary jet lag, canine circadian desynchronization, zeitgebers, air transport stress, feline chronobiology, canine HPA axis, social jetlag pets, veterinary actigraphy.

Section 1 Operational definition: «jet lag» as a clinical label

1.1 Human jet lag and the limits of extrapolation

Jet lag in human medicine is a well-defined chronobiological syndrome, produced by rapid displacement across multiple time zones and characterised by misalignment between the individual's internal clock and local environmental time. Its manifestations include insomnia or hypersomnia, fatigue, cognitive impairment, gastrointestinal alterations and irritability. The central pathophysiology involves the suprachiasmatic nucleus (SCN) of the hypothalamus, which acts as the central pacemaker of the circadian system and resynchronises more slowly than environmental stimuli after an abrupt time-zone change.

The use of the term «jet lag» in the veterinary context is functionally descriptive but scientifically imprecise. For the human syndrome to be directly extrapolable to a dog or cat, at least two conditions would need to be met: that the animal has an equivalent functional SCN with similar resynchronisation properties, and that the animal subjectively experiences temporal misalignment. The first condition is reasonably supported by anatomical and physiological evidence; the second cannot be verified with current tools.

This article therefore adopts a conservative and verifiable position: to speak of circadian desynchronization and transport stress as documented or plausible mechanisms, using «jet lag» exclusively as an operational term for outreach.

1.2 Two mechanisms, not one: circadian desynchronization vs. acute transport stress

It is conceptually important to distinguish the two mechanisms that converge in the animal that has just completed a long-haul transmeridian flight:

Circadian desynchronizationAcute transport stress
MechanismMismatch between the internal clock and the zeitgebers of the new environment (light, feeding schedules, activity routine).Activation of the SAM and HPA axes by the physical and environmental stressors of travel: confinement, noise, motion, temperature, pressurisation, water and food deprivation.
Temporal scaleDays to weeks (gradual resynchronisation process).Hours to 2-3 days (recovery from acute stress response, according to Leadbeater et al., 2021).
Evidence in dogs/catsIndirect (social jetlag in dogs, Wenchner 2024). Biological inference for transmeridian flights.Direct and documented (Leadbeater 2021; Wormald 2017; Beerda 1998).
ManifestationsSleep alterations, behavioural changes, temporal disorientation.Elevated cortisol, tachycardia, panting, inappetence, GI changes, lethargy.

In pet relocation practice, both mechanisms coexist and reinforce each other. An animal that arrives stressed in the new environment has compromised capacity to resynchronise quickly because stress itself alters circadian rhythms. This overlap is why the post-flight adaptation period cannot be simplified to a single linear process.

Section 2 Relevant chronobiology fundamentals

2.1 The central clock: suprachiasmatic nucleus (SCN)

The mammalian circadian system is organised hierarchically. The SCN of the anterior hypothalamus acts as the master pacemaker: it integrates light information received via the retinohypothalamic tract and coordinates peripheral clocks present in virtually all tissues of the organism (liver, intestine, muscle, skin). This architecture is evolutionarily conserved in all mammals, including dogs and cats, making it biologically plausible —though not specifically proven for transoceanic flights— that perturbations in SCN input stimuli produce desynchronization in these species.

Peripheral clocks can desynchronise from each other and from the SCN when the zeitgebers that govern them do not change simultaneously. This is precisely what happens in a transmeridian flight: light in the new environment can change abruptly, but feeding schedules, ambient temperature and owner activity patterns adapt at different rhythms. The result is internal discoordination that, in humans, produces measurable symptoms.

2.2 Zeitgebers: the synchronizers of the biological clock

The term zeitgeber (from German: «time giver») designates the environmental stimuli that synchronise the internal clock with the 24-hour environmental cycle. In mammals, the main zeitgebers are:

The relevance of listing zeitgebers in the context of air transport is that all of them are perturbed simultaneously during a long-haul flight: light exposure changes (dimmed cabin or artificial light), the animal may not receive food for 8-12+ hours, cargo hold temperature varies, and social interaction with the owner is nil or minimal. The flight is, in this sense, a simultaneous multizeitgeber perturbation.

2.3 What we know about dogs and cats: documented rhythms

Dogs: Zanghi (2016) demonstrated through 24-hour activity monitoring that the domestic dog has a diurnal-crepuscular rhythm pattern but one highly mouldable by the owner's schedule. This adaptability, which favours cohabitation, also implies that the dog is especially vulnerable to desynchronization when the owner's schedules change abruptly —exactly what happens in a time-zone change.

Social jetlag in dogs (Wenchner et al., 2024): This study published in Scientific Reports is the most relevant and recent finding for this article. The authors documented that dogs whose owners change their schedules between weekdays and weekends (the so-called human «social jetlag») show measurable alterations in sleep quality and activity patterns. This is the first study to demonstrate directly that dogs suffer circadian desynchronization in response to changes in human cohabitation schedules — a mechanism directly analogous, though not identical, to that triggered by a transmeridian flight.

Cats: Piccione et al. (2013) documented the circadian body temperature rhythm in domestic cats, confirming a crepuscular pattern with activity peaks at dawn and dusk. Randall et al. (1985) demonstrated that the light/dark cycle is the dominant regulator of feline activity, with greater adaptive rigidity than in the dog. This lower plasticity makes the cat potentially more vulnerable to abrupt light perturbations such as those produced by a night flight across multiple time zones.

Extrapolation limit — explicit statement Everything described in this section regarding post-transmeridian-flight circadian desynchronization in dogs and cats is a plausible biological inference based on mechanisms conserved among mammals. There are no pre/post-transmeridian-flight actigraphy studies in dogs or cats. Extrapolation from human and rodent chronobiology is stated and methodologically justified, not concealed.

Section 3 The stress–rhythm axis: SAM and HPA as bridge

3.1 Acute response to transport: direct evidence in dogs

Unlike circadian desynchronization per se, the physiological impact of air transport stress in dogs is documented with direct evidence of acceptable quality.

Leadbeater et al. (2021, Veterinary Record): This is the most comprehensive study available on canine welfare during transport. The authors documented salivary cortisol peaks during and after air transport, with values that in some individuals took up to 48 hours to return to baseline. This finding has direct practical implications for the post-arrival observation period.

Wormald et al. (2017, Applied Animal Behaviour Science): Quantified tachycardia and panting as markers of SAM (Sympathetic-Adreno-Medullary) axis activation in dogs during transport. These parameters are indicators of acute sympathetic activation, consistent with the initial phase of the stress response: release of adrenaline and noradrenaline by the adrenal medulla.

Beerda et al. (1998, Physiology & Behavior): Established the reference parameters for urinary and plasma cortisol response in dogs under environmental stressors, including confinement and novelty. It is the methodological reference that allows interpretation of cortisol values in more recent studies.

3.2 The bidirectional interaction between stress and circadian rhythms

Extrapolation note: the mechanism described in this section is mainly documented in humans and rodents. Its application to dogs and cats is stated as a biological inference based on evolutionarily conserved mechanisms.

The relationship between the stress axes and the circadian system is bidirectional and of particular relevance for understanding why the post-flight adaptation period is more complex than simply resetting a clock:

Pastore et al. (2011, Animal Welfare): This study confirmed that the dog has a circadian cortisol rhythm similar to the human, with a morning peak. This basis is essential to be able to speak of «HPA axis desynchronization» as a plausible phenomenon when the dog arrives in a time zone where the «morning peak» should occur at a time that its internal clock still registers as another time of day.

3.3 Stress and its effects on sleep, appetite and gastrointestinal motility

Transport stress can explain, through well-documented mechanisms, three of the most frequently reported manifestations in the post-flight period:

Section 4 Observable phenotypes post-travel

This section describes the behavioural and physiological alterations frequently reported by owners and veterinarians in the immediate post-flight period (first 24-72 hours) and in the intermediate adaptation period (approximately days 3-14). The language used is deliberately conservative: manifestations are described as «frequently reported» or «compatible with» the mechanisms described, not as causally established consequences.

4.1 Sleep and wake alterations

These are the manifestations most directly related to circadian desynchronization and the most frequently reported in dogs that have completed transmeridian flights of more than 6 time zones:

4.2 Inappetence and intake changes

Inappetence in the first 12-24 hours post-travel is a frequently reported manifestation and biologically coherent with residual sympathetic activation and prolonged fasting during the flight. In most cases, appetite normalises within 24-48 hours. Changes in the timing of food demand (the animal asks for food at times that do not correspond to its new environment) are compatible with persistence of the gastrointestinal peripheral clock circadian rhythm. Since feeding schedules are a zeitgeber, irregularity in meals in the post-travel period may prolong desynchronization.

4.3 Gastrointestinal changes

Soft or variable-consistency faeces, isolated vomiting episodes and flatulence are frequently reported in the post-travel period. Interpretation of these signs must be made in the context of the complete journey: pre-travel fasting (many airlines and protocols recommend food restriction 4-8 hours before the flight; prolonged fasting followed by refeeding can produce transient changes in motility and microbiota); travel stress (HPA axis activation alters GI motility and may temporarily compromise intestinal epithelial barrier function); water change (water at the new destination may have different mineral composition). The presence of persistent GI signs (beyond 48-72 hours), haematemesis, melaena or systemic signs requires veterinary evaluation.

4.4 Behavioural alterations: hypervigilance, lethargy and vocalisation

Hypervigilance and excessive exploration: compatible with residual sympathetic activation and the biological need to map a new environment. Lethargy: frequent in animals whose travel stress was more intense or prolonged; compatible with the exhaustion phase that follows sustained HPA axis activation. Nocturnal vocalisation: especially in dogs with predisposition to separation anxiety; compatible with the combination of temporal disorientation and residual activation. Inattention or apparent disorientation: compatible, according to Kis et al. (2014), with REM sleep alteration and its role in spatial and contextual memory consolidation.

Clinical note The manifestations described in this section are frequently reported and biologically coherent. However, none is pathognomonic of «jet lag» nor can be diagnosed as such in the absence of ruling out other causes. Differential diagnosis for any symptomatic animal post-travel must always be performed by a veterinarian, also considering infectious diseases acquired in the country of origin or transit, intoxications, transport trauma and pre-existing pathologies decompensated by stress.

Section 5 Differences by species and physiological state

5.1 Dogs vs. cats: differential tolerance to routine change

ParameterDogsCats
Activity patternDiurnal/crepuscular, highly adaptable to human schedule (Zanghi, 2016)Fundamentally crepuscular, with greater adaptive rigidity (Randall, 1985)
Circadian plasticityHigh: canine rhythm can be modulated by owner social jetlag (Wenchner, 2024)Lower: light/dark cycle is the dominant regulator
Response to transport stressDocumented: cortisol and cardiorespiratory parameters (Leadbeater 2021, Wormald 2017)Less studied; rupture of the bond with the known environment elevates stress response (Vitale, 2019)*
Tolerance to confinementVariable; correlates with temperament and prior conditioningGenerally lower; the territory-dependent cat is more vulnerable
Expected resynchronisation speedInferred: hypothesis of 2-5 days for 6-12 time-zone changes (extrapolation from human model)Inferred: possibly slower due to lower circadian plasticity; not quantified

* Vitale et al. (2019, Current Biology): study on the attachment bond between cats and humans. Used here as a conceptual framework to argue that rupture of the known environment activates the stress response in cats. Not an air transport study; stated as framework reference, not direct evidence.

5.2 Vulnerability factors: puppies, geriatrics and chronic disease

Puppies (< 6 months): the circadian system is not fully mature; the stress response may be more intense; prolonged fasting has more severe metabolic consequences in young small-sized animals. Geriatric animals (> 8-10 years): Bognár et al. (2021) documented that sleep fragmentation increases with age in dogs; geriatrics may have a slower resynchronisation window. Chronic disease: pathologies affecting the HPA axis, CNS, GI tract or renal function may decompensate due to transport stress. Brachycephalic breeds: upper airway compromise amplifies transport stress under elevated temperature or confinement conditions.

Section 6 Magnitude of time-zone change: a risk model

Methodological note: the relationship between number of time zones and magnitude of desynchronization is well documented in humans. Its application to dogs and cats is presented as a working hypothesis applied to routine desynchronization, not as a proven fact in these species.

In human medicine, jet lag severity correlates with: (a) the number of time zones crossed, (b) direction of travel (eastbound flights generate greater desynchronization than westbound), and (c) individual traveller characteristics. Applying this framework as a working hypothesis to companion animals:

CategoryTime-zone changeExpected implication for routines
Low1-3 time zonesMild mismatch in feeding and walking schedules. Resynchronisation expected in 1-3 days with maintenance of routines.
Moderate4-7 time zonesSignificant mismatch of the light/dark cycle. Sleep and appetite alterations likely for 3-7 days. Requires active zeitgeber management.
High8-12+ time zonesMaximum mismatch, including potential partial cycle inversion. The adaptation period may extend to 7-14 days. Vulnerability amplified in geriatrics and puppies.
Application of this model This risk categorisation is a logistical planning tool based on the human jet lag framework, applied by analogy to routine desynchronization in animals. It has not been experimentally validated in dogs or cats. It should be used as an orientative guide to anticipate the adaptation period, not as a precise clinical predictor.

Section 7 Re-entrainment: how an animal realigns

Re-entrainment is the process by which the circadian system resynchronises with the zeitgebers of the new environment. In humans, the rule of thumb is approximately one day of adaptation per time zone crossed. In dogs and cats, this parameter has not been specifically measured.

7.1 The role of zeitgebers in resynchronisation

Light/dark cycle: exposure to natural light in the new environment at the correct times of day (morning at destination) accelerates SCN resynchronisation. Feeding schedules: maintaining regular schedules adapted to the new time zone from day one activates one of the most relevant zeitgebers for peripheral clocks. Activity and socialisation routines: maintaining regular walking, play and interaction routines at the new destination's times provides social and activity zeitgeber signals. Expected time frame (working hypothesis): in the absence of specific data for dogs and cats, it is reasonable to estimate that healthy adult animals achieve functional resynchronisation in a period of 3 to 10 days for 6-12 time-zone changes, with significant individual variability.

7.2 Melatonin: position in the evidence

Dunlap et al. (2015, AJVR): documented that endogenous melatonin plasma levels in dogs are significantly lower than in humans. This quantitative difference questions the direct extrapolation of human dosing protocols to the dog. There is no controlled clinical trial that has evaluated exogenous melatonin for post-flight resynchronisation in dogs or cats. Melatonin is not prescribed or recommended in this article. It is stated as an area with insufficient evidence for the specific use of air jet lag in pets.

Section 8 Implications for transport and owners

8.1 Variables that the owner and operator can control

Controllable variableChronobiological and stress relevance
Time of arrival at destinationArriving in the morning or early afternoon at destination facilitates correct light exposure from day one.
Duration of layovers and waitsProlonged airport waits amplify sustained HPA axis stress. Direct routes or short layovers reduce total duration of stress activation.
Prior familiarisation with the crateAn animal that perceives the crate as a safe space has a significantly lower stress response during the flight.
Transport environment temperatureComfort temperatures (18-24°C) reduce the total physiological load of the journey.
Pre-flight hydrationWater fasting should be minimised. Dehydration amplifies the stress response.
Keeping the owner's scentAn item with the owner's scent in the crate acts as a social safety signal and reduces SAM axis activation.

8.2 What happens inside the cargo hold

Lighting: practically nil or very low; the animal is in darkness for most of the flight. Noise: the level in cargo holds is high (70-85 dB or more in cruise); it is a significant and sustained stressor. Temperature: regulated in animal-eligible cargo holds according to IATA standards, but with variability during tarmac embarkation/disembarkation. Pressurisation: equivalent to approximately 1,500-2,400 m altitude; there is no evidence that relative hypoxia at this altitude has relevant clinical impact in healthy animals.

Declared evidence gap There are no actigraphy or physiological monitoring studies conducted during flight inside the cargo hold. Everything we know about the animal's physiological state during the flight comes from environmental inferences and post-travel measurements.

8.3 The first 48 hours at destination

Prioritise access to clean water at destination immediately upon arrival. Do not force feeding if the animal shows inappetence in the first 4-6 hours. Expose the animal to natural light in the new environment during daytime hours at destination. Maintain destination routines (meal times, walks) from day one, not adapted to origin time. Reduce additional stressors: visits, environment changes, introductions to other animals. If GI signs, inappetence or behavioural alterations persist beyond 48-72 hours, consult a veterinarian at destination.

Section 9 Limitations and evidence hierarchy

9.1 Map of available evidence

Claim / MechanismType of evidenceMain source
Air transport elevates cortisol in dogs for up to 48hDirect evidence — study in dogsLeadbeater et al. (2021)
Transport induces tachycardia and panting in dogsDirect evidence — study in dogsWormald et al. (2017)
Dogs have circadian cortisol rhythm with morning peakDirect evidence — study in dogsPastore et al. (2011)
The dog has measurable chronotype; sleep fragments with stressDirect evidence — study in dogs (actigraphy)Bognár et al. (2021)
Human social jetlag desynchronises dog sleepDirect evidence — study in dogsWenchner et al. (2024)
The cat is crepuscular with circadian body temperature rhythmDirect evidence — study in catsPiccione et al. (2013)
Light/dark cycle regulates cat activityDirect evidence — study in catsRandall et al. (1985)
Cortisol desynchronises peripheral clocksHuman/rodent evidence — STATED EXTRAPOLATIONGeneral chronobiology literature
A transmeridian flight produces jet lag in dogs/catsNO direct evidence — biological inferenceTheoretical model built in this article
Post-flight resynchronisation time in dogs/catsNO direct evidence — working hypothesisExtrapolation from human model

9.2 Declared evidence gaps

The five most relevant evidence gaps: (1) Real jet lag in cats: there are no studies of physiological desynchronization by time-zone change in domestic cats. (2) Melatonin and air jet lag: there is no controlled clinical trial that has evaluated exogenous melatonin for post-flight resynchronisation in dogs or cats. (3) Intestinal microbiota and time-zone change: there is no equivalent evidence in dogs or cats. (4) Resynchronisation kinetics: the exact biological resynchronisation time post-transmeridian flight in dogs and cats is unknown. (5) Physiology during flight: there are no actigraphy or continuous cortisol, heart rate or temperature monitoring studies conducted during flight in the cargo hold.

Section 10 Research priorities

Longitudinal actigraphy studies pre/during/post-flight; non-invasive biomarkers (salivary and faecal cortisol with serial sampling); heart rate variability (HRV) as an indicator of autonomic activation; comparative dog vs. cat studies under controlled time-zone change conditions; non-pharmacological zeitgeber interventions evaluated with biomarkers.

Editorial self-verification 10-point checklist

Declared scope. Species dog and cat. «Jet lag» as operational label; no direct extrapolation of human syndrome.
Two mechanisms differentiated. Circadian desynchronization vs. acute transport stress; comparative table present.
Zeitgebers. Correct chronobiological terminology; zeitgeber explained (time giver).
HPA/SAM. Sympathetic-Adreno-Medullary and Hypothalamic-Pituitary-Adrenal axes translated and used coherently.
Extrapolation limit. Explicit warning box: biological inference, no pre/post-flight actigraphy studies in dogs/cats.
Direct evidence cited. Wenchner 2024, Leadbeater 2021, Bognár 2021, Piccione 2013, Randall 1985, Pastore 2011, Wormald 2017, Beerda 1998, Dunlap 2015.
Clinical note. No pathognomonic manifestation; differential diagnosis by veterinarian.
Melatonin. Not prescribed or recommended; insufficient evidence stated.
Evidence hierarchy. Table 9.1 and evidence gaps stated in section 9.2.
Dual authorship. Jessica Ysabel Camacho Garcia (CMVP 12434) and Víctor Jesús Camacho Paz (CMVP 3103) in header and JSON-LD.

References

  1. Wenchner, J., et al. (2024). Evidence of social jetlag in family dogs. Scientific Reports. https://doi.org/10.1038/s41598-024-52648-2
  2. Leadbeater, K., et al. (2021). The welfare of dogs during transport. Veterinary Record. https://doi.org/10.1002/vetr.611
  3. Bognár, Z., et al. (2021). The effect of age and chronotype on the sleep of family dogs. Animals, 11(9). PMID: 34504118
  4. Wormald, D., et al. (2017). Physiological and behavioral responses of dogs to transport. Applied Animal Behaviour Science, 189, 78–87. https://doi.org/10.1016/j.applanim.2017.02.003
  5. Pastore, C., et al. (2011). Diurnal cortisol rhythm in family dogs. Animal Welfare, 20(3), 371–376.
  6. Kis, A., et al. (2014). The interrelated effect of sleep and learning in dogs: an EEG and behavioural study. Scientific Reports / Proc. Biol. Sci. PMID: 24452026
  7. Beerda, B., et al. (1998). Manifestations of chronic and acute stress in dogs. Physiology & Behavior, 63(2), 245–253. PMID: 9657571
  8. Zanghi, B. M. (2016). Twenty-four hour activity patterns in dogs. Journal of Veterinary Behavior, 11, 14–20. https://doi.org/10.1016/j.jveb.2015.09.004
  9. Dunlap, N. E., et al. (2015). Circadian variation of melatonin in dogs. American Journal of Veterinary Research, 76(1), 67–72. https://doi.org/10.2460/ajvr.76.1.67
  10. Piccione, G., et al. (2013). Daily rhythm of body temperature and activity in cats housed in a domestic environment. Journal of Feline Medicine and Surgery, 15(9), 798–802. https://doi.org/10.1177/1098612X12470535
  11. Andrews, J. S., et al. (2015). Validation of accelerometry as a measure of activity in cats. Journal of Feline Medicine and Surgery, 17(9), 767–774. https://doi.org/10.1177/1098612X14552435
  12. Randall, W., et al. (1985). The effect of season and light on the cat's circadian rhythm. Reviews in Veterinary Science, 38, 279–285.
  13. Vitale, K. R., et al. (2019). Attachment bonds between domestic cats and humans. Current Biology, 29(18), R864–R865. https://doi.org/10.1016/j.cub.2019.08.036
  14. Reppert, S. M., & Weaver, D. R. (2002). Coordination of circadian timing in mammals. Nature, 418, 935–941. https://doi.org/10.1038/nature00965
  15. Albrecht, U. (2012). Timing to perfection: the biology of central and peripheral circadian clocks. Neuron, 74(2), 246–260. https://doi.org/10.1016/j.neuron.2012.04.006
  16. Buijs, R. M., & Kalsbeek, A. (2001). Hypothalamic integration of central and peripheral clocks. Nature Reviews Neuroscience, 2, 521–526. https://doi.org/10.1038/35081582
  17. Thaiss, C. A., et al. (2014). Transkingdom control of microbiota diurnal oscillations promotes metabolic homeostasis. Cell, 159(3), 514–529. https://doi.org/10.1016/j.cell.2014.07.044