Studies of locomotor activity in Svalbard reindeer reported the temporary absence of diel rhythms under Arctic photic conditions. However, using Lomb-Scargle periodogram analyses with high statistical power we found diel or circadian rhythmicity throughout the entire year in measures of behaviour, temperature in the rumen and heart rate in free-living Svalbard reindeer. Significant diel rhythmicity was only lacking during some of the 15-day intervals analysed in the less frequently measured heart rate. During Polar Night these rhythms were free-running and attenuated. During continual daylight in summer, rhythms where entrained to 24 hours corresponding with the daily variation in the intensity of solar radiation, but attenuated when continuous daylight coincided with the period of growing forage. Diel rhythmicity was reduced during this short period of peak foraging activity, which coincided with peak heart rate and temperature in the rumen, most likely to facilitate fattening when food is abundant. For the rest of the year, heart rate and temperature showed the most pronounced and long-lasting suppression ever found in ungulates. The profound seasonal changes in foraging, metabolic activity, and power of diel and circadian rhythmicity of Svalbard reindeer can be viewed as adaptations to the extreme living conditions in the High Arctic.
Ever since its earliest beginnings, the temporal organisation of life has been shaped by the Earth’s rotation and orbit. No other change in the environment alters the living conditions more, and is more predictable, than the 24 hour light/dark cycle and the annual photoperiod cycle. These cycles are the main drivers in the evolution of endogenous clocks enabling anticipation of the Earth’s periodicities. Circadian clocks are entrained to diel rhythms of 24 hours by external cues (zeitgebers). In polar areas, however, a day/night cycle is absent for much of the year. Therefore, the circadian clock is expected to free-run, i.e. circadian rhythms of activity or physiological functions are expected to show period lengths slightly deviating from 24 hours in the absence of 24-hour zeitgebers1.
The Arctic represents a most extreme environment, particularly for endothermic herbivores. Primary production is typically low and restricted to the short summer period when the ground is snow-free and temperatures are above freezing2. For most of the year, the weather is much harsher and particularly during mid-winter, when the sun does not rise above the horizon (Polar Night), the ground is frozen, and snow or ice restrict access to food. During the nutritional bottle-neck of winter many herbivorous mammals depend on body fat reserves for energy and insulation3,4, which are accumulated during summer. Among ungulates, summer fattening is most pronounced in Arctic species, like reindeer3. Therefore, in the Arctic, natural selection may have favoured abandoning diel rhythmicity during the summer period of continual daylight (Midnight Sun) in order to optimally exploit the short time window of plant growth and to maximise energy intake. Indeed, an apparent lack of circadian rhythmicity during seasons of continual darkness or daylight has been reported for a number of Arctic species5, and it has been concluded that the loss of circadian rhythmicity may be an ubiquitous trait among resident Polar vertebrates6. However, these studies focussed only on the temporal organisation of activity patterns, and did not address the role of food availability.
Here we present results from our long-term study not only of behaviour, but, for the first time, also of physiological variables in Svalbard reindeer (Rangifer tarandus platyrhynchus). We demonstrate with high sampling rates the continuous existence of diel rhythmicity not only during periods of day/night cycles but also during continual light, and free-running circadian rhythmicity during Polar Night. However, these rhythms are attenuated by continual darkness in winter and the availability of growing forage in summer.
Strong seasonality was found in all variables measured, with distinct peaks during the short summer and low values during the rest of the year, with some differences between years and individuals associated with reproductive status (Fig. 1 and Table 1). Daily mean heart rate of animals at rest or moving slowly (‘stationary’ heart rate, HRs), more than doubled (126%) within 65 days from mid-May till mid-July from a baseline of ~40 bpm to more than 90 bpm (Fig. 2). In contrast, the increase from the winter baseline through to the summer peak was small for ruminal temperature, Trumen (2%), and moderate for activity (39%), occurring within 77 and 140 days, respectively. The number of vertical head movements during 3-minute measurement intervals increased to the summer peak by 101% within 65 days (Fig. 1).
Phase relations of the variables measured were explored by comparing baseline cosine functions fitted to the empirical data (Fig. 2). The onset of the summer period of high HRs (95% confidence interval [CI] May 7–16) coincided with the onset of high Trumen (95% CI May 12–15), and high numbers of vertical head movements (95% CI May 11–16). The end of the period of high HRs (95% CI Sep 23–25) occurred on average 21 days before the end of the period of high Trumen (95% CI Oct 14–17), and 4 days after the period of high numbers of vertical head movements (95% CI Sep 17–22). The onset of the period with high ambient temperature, measured in the collar, Tcollar, (95% CI Apr 1–7) coincided with the beginning of continual light (Apr 5), and ended slightly before the return of continual darkness (95% CI Nov 5–11) on Nov 15. However, activity began to increase from the winter low by mid-March (95% CI Mar 12-Apr 1), a few days before Tcollar began to rise, and remained above the winter baseline until Dec 19-Jan 8 (95% CI), i.e., way into the period of continual darkness and lowest Tcollar.
Daily and circadian rhythms
Rhythms with a period length (τ) of ~24 h, causing significant periodogram peaks at p < 0.05, were found throughout the year and in all variables measured (Figs 3a and 4, Supplementary Figs S1–S3). Only for HRs, which was less frequently measured, were no significant rhythms in the 21–27 h range detectable in some of the 15-day intervals analysed (Fig. 3a). In order to discriminate between the influences of continual daylight and food availability on the rhythmicity of physiological and behavioural variables, the period from April 5 to September 7 (Midnight Sun) was divided into two parts according to the Normalized Difference Vegetation Index (NDVI, Fig. 2). During the first part, to early June, food availability resembled that typical for winter (NDVI values <0), whereas during the second part from early-June to early-September, NDVI values >0 indicated growing vegetation (Fig. 2). During the first part of the period with continual daylight but little or no new plant growth, clear 24 hour rhythmicity was present in both behavioural and physiological measurements (Figs 3a, 4 and 5, Supplementary Figs S1–S14), in the case of Trumen even with the highest normalized power (Fig. 3a and Supplementary Fig. S2). Diel rhythmicity persisted but became weaker during the second part, when most vegetation growth occurred, and when the daily variance of solar radiation was lowest (Figs 3, 4 and 5, Supplementary Figs S1–S14). With respect to entrainment, HRs was again an exception with apparently low or lacking entrainment to 24 hours during Midnight Sun (Fig. 3a and Supplementary Fig. S3). The daily variation of solar radiation, peaking at begin and end of the period of Midnight Sun (Fig. 3d), was an important predictor of the power of diel rhythmicity, as were high values of NDVI for its attenuation during the period of continuous daylight (Table 2).
As expected, when reindeer were exposed to daily light/dark cycles (end of January to early April, early September to mid-November, see first panel in Fig. 5), all physiological and behavioural variables measured showed strong diel rhythmicity with a τ of 24 hours (Figs 3a and 4, Supplementary Figs S1–S3). During the period of Polar Night, temporal organisation of physiological and behavioural variables remained rhythmic, but with lower normalized power, similar to rhythms found during the second part of the period with continual daylight and high values of NDVI (Fig. 3a). However, in contrast to the period of Midnight Sun, during the Polar Night the significant peaks almost always had a τ ≠ 24 hours (Fig. 4, Supplementary Figs S1–S3).
Ultradian rhythms with τ between ~4–8 hours were present throughout the year with strong normalized power in locomotor activity and changes of head positions during three-minute measurement intervals. During winter the dominant period of these rhythms was ~6 hours and shortened to ~4 hours during the summer period (Fig. 5, Supplementary Figs S4–S8). In contrast, ultradian rhythmicity was less pronounced in Trumen and HRs (Supplementary Figs S9–S14).
Our results clearly demonstrate that rhythmicity with τ of ~24 h persists throughout the year in Svalbard reindeer. This is at odds with previous reports of an apparent lack of such rhythmicity in this species in the absence of a day/night cycle6,7,8. However, the power of this rhythmicity diminished considerably during Polar Night and a τ of typicall y ≠ 24 hours indicated free-running endogenous circadian rhythmicity. Conversely, rhythms remained well entrained during continual light conditions in summer, except for HRs, and had a high power before the onset of the plant growing season (Fig. 3a,b). Diel rhythmicity diminished later reflecting the need for intense foraging all around the clock when forage availability and quality was at its best. The attenuation of rhythmicity also coincided with minimal daily variance in solar radiation. However, continual light, i.e. a loss of zeitgeber, is unlikely to be solely responsible for the attenuation of rhythmicity during June to August, because we found no indication of free-running rhythms as in winter. Therefore, we attribute the apparent diminution of daily rhythms to foraging requirements. However, even then diel rhythmicity persisted as can be seen particularly in the 24 hour rhythmicity of Trumen (Fig. 3a and Supplementary Fig. S2). The summer period with high values of HRs, Trumen, and locomotor activity in Svalbard reindeer is the shortest ever found in ungulates so far (Fig. 6). Furthermore, the difference of HRs and Trumen between winter and summer is the most pronounced among the species where this has been measured9,10,11,12,13. Presumably the extremely short time-window during which plant growth is sufficient for fattening requires Svalbard reindeer to attenuate diel rhythmicity and feed throughout 24 hours, thereby largely ignoring their circadian master clock, even though this is still running.
The spring increase of locomotor activity clearly preceded that of physiological variables and vertical movements of the head, i.e. food intake. Also, it preceded the spring increase of collar temperature (Tcollar), although low ambient temperatures basically reduced locomotor activity. Similarly, activity remained high until around the winter solstice, despite Tcollar being close to the winter low from the end of November onwards. The reason for the much wider peak of activity compared to other variables remains enigmatic. Seasonal migration would be a possibility, but can be excluded for Svalbard reindeer14. Although severe winter weather, particularly ‘icing events’ associated with ‘rain-on-snow’, may cause local animal movement (5–10 km) to seek accessible forage15,16, Svalbard reindeer are regarded as basically sedentary14. Populations separated by as little as 40–50 km are genetically distinct17.
The frequency of vertical movements of the head increased about two weeks before the increase in NDVI. The food ingested during these two weeks will have been the standing crop from the previous summer with some new shoots of plants growing on ridge communities, where snow melt is earliest2. Therefore, the marked increase of foraging activity before substantial new growth of plants became available, suggests photoperiodic control of appetite, as described for many other ungulates13,18,19,20.
Our results indicate the continuous function of the circadian clock throughout the year in Svalbard reindeer, but the animals barely adhere to it under certain circumstances. During the period of Midnight Sun, entrainment to a 24 hour period was evident, despite continual daylight. In the absence of a day/night cycle changes in ambient temperature, which can entrain the circadian clock in rodents, e.g.21, did not act as alternative zeitgebers (Table 2). Possibly, the cyclic diel changes of solar radiation (Fig. 3d and Table 2), or associated changes of luminance or skylight colour22,23,24 may act as zeitgebers. However, these cues failed to entrain circadian rhythms in another Arctic species, the Lapland Longspur25,26, that shows persistent daily rhythms in activity and melatonin production und continuous illumination in summer.
During the Polar Night these potential alternative zeitgebers were absent, at least around the winter solstice. As a result, circadian rhythms were free-running with τ deviating from 24 hours and with different τ for HRs, Trumen and behavioural measures within individuals (Fig. 5, Supplementary Figs S1–S3), suggesting internal desynchronization of rhythms27,28. Multiple significant peaks during the Polar Night with τ of ~24 h indicate different but fairly stable τ across the mid-winter months. Such shifts of individual τ are well known, for example as ‘after effects’, typically occurring when an organism is transferred from an environment with distinct zeitgebers into one without29. Our findings support the view by Williams et al.5 that persistent circadian rhythms in continual darkness may be adaptive due to interdependence between circadian clock function and homeostatic processes.
In line with previous reports6,7,8, we found strong and similar ultradian rhythms in activity and vertical movements of the head, with seasonally changing period lengths. Shorter period lengths were present during peak vegetation growth and probably indicate more frequent fills of the gut, greater digestibility and hence shorter gut passage time when food is abundant and of high quality6,20,30.
The reason for the discrepancy between our results and previous reports seems to be partly due to a difference in statistical power resulting from both sample size and type of periodogram analysis applied. Loe et al.8 recorded hourly activity only every 5th day and created time series by merging these measurement days. This lack of continuous monitoring presumably prevented the detection of weak diel rhythmicity. We also failed to find significant diel rhythmicity throughout continual light or darkness, presumably due to insufficient sample size, in the less frequently measured HRs (every 21 minutes compared to 3 minutes for activity, and only if the animal was at rest or moving slowly) in individual #2 (Supplementary Fig. 3), or in some 15-day intervals (Fig. 3a). Van Oort et al.6,7 on the other hand, recorded activity at 10–15 minute intervals but evaluated their data with F-periodogram analysis. The algorithm underlying this method is actually mathematically equivalent to the Chi2-periodogram31, and this method is known to have poor power to detect existing rhythms compared with the Lomb-Scargle periodogram32. We used the Lomb-Scargle periodogram because this method is particularly suited to detect periodic components in unequally sampled time-series and data sets with missing values, but restricts all calculations to actually measured values. Therefore, Lomb-Scargle periodogram analysis is superior to other statistical methods applied in biomedical rhythm research, including Fourier analysis e.g.8, if data are obtained over longer periods of time which typically have such features32.
Taken together, our data suggest that the circadian master clock in reindeer continues to function throughout the year, but daily cycles are easy to detect only in variables with a high signal to noise ratio, such as Trumen, and if data are sampled frequently. However, these results do not rule out that certain other diurnal rhythms in reindeer, such as the production of melatonin, are not governed by the circadian system as typical for rodents, but by acute responses to the light/dark cycles33. This type of regulation of the melatonin rhythm, which has been demonstrated in captive reindeer33, may well represent an adaption to a weak output of the circadian axis under certain photic conditions, but is not evidence for a complete absence of circadian clock signals.
To summarize, the length of the metabolically intense summer phase of Svalbard reindeer is the shortest found in ungulates so far, and the differences between summer and winter in physiology and behaviour are the highest ever reported. Diel rhythmicity persists throughout the year, although attenuated by continual darkness and high availability of food. During these periods, temporal organisation of behaviour and physiology was to a large degree shaped by ultradian rhythms of foraging behaviour.
Study area and climate
The research was carried out in Nordenskiöldland, Svalbard (77°50′–78°20′N, 15°00′–17°30′E). Our main study area was centred in Colesdalen, Semmeldalen, and parts of Reindalen, and their side-valleys. The generally wide, U-shaped valleys are mostly vegetated (up to about 250 m altitude), though the short growing season means that above-ground live vascular plant biomass in vegetated habitats averages only 35 g per m2 (annual range 23–46 g per m2)2. Nonetheless, the area supports a relatively high density of reindeer compared to other parts of Svalbard34 with the population almost doubling over two decades35. The lower-lying, wetter, and more productive, pastures are grazed during summer, but in winter forage tends to be less accessible here because of deep or hard snow, or ice. Therefore, in winter reindeer tend to feed on wind-blown vegetated ridges, and at higher elevations see also36.
Direct maximum solar radiation at the study site as a function of the day of year and time of day (disregarding weather effects), was computed using equations given at www.pveducation.org. These computations involve calculating the sun’s zenith angle, for which we used function SZA from the R package RAtmosphere37.
Remote-sensed vegetation indices
We used remote-sensed values of the Normalized Difference Vegetation Index (NDVI) between April 2012 and May 2014 for the valleys Colesdalen, Semmeldalen, and Reindalen in our study area. The NDVI values from the MODIS Terra platform are based on 16-day composites on a spatial resolution of ~250 m available from (https://search.earthdata.nasa.gov), and are above zero from the start of snow melt in June until October when failing light levels limit the records.
The four animals sampled in this study were instrumented with GPS-collars (Vectronic Aerospace) at time of capture, which were modified by the Research Institute of Wildlife Ecology. The modification consisted of adding two components, a cylindrical ruminal unit (22 × 80 mm, 100 g) to record physiological measurements, and a unit situated in one of the collar’s battery slots, used for communication with the ruminal unit, data storage and for measuring activity. Activity of the animals and vertical movements of the head were detected in the collar unit with a tri-axial vibration switch, and a mercury switch, respectively. Activation of these switches was checked every second. The proportion of activations of the tri-axial vibration switch during a 3-minute measurement interval was our measure of locomotor activity. The mercury switch was activated by tilting the perpendicular position of the collar by more than approximately 15 °C. The number of activations of the mercury switch (head up/down movements) during a 3-minute measurement interval was our indicator of grazing activity. Lastly, a temperature sensor in the black instrument and battery case of the collar, located under the animals’ head, measured ambient temperature (Tcollar). Numbers of activations of the tri-axial vibration switch, of the head-movement mercury switch, and mean Tcollar during 3-minute measurement intervals were stored in the collars’ solid–state memory.
The ruminal unit was introduced into the pharynx with an applicator and then swallowed by the reindeer into the reticulum. Temperature in the rumen (Trumen) was measured every 3 minutes by a thermistor in the ruminal unit, calibrated in a water bath before administration at 5 °C-increments between 20–40 °C with an accuracy of 0.1 °C. Trumen measurements contained brief periods of rapid cooling because of ingested cold water, snow or food. We discarded these data from analyses by removing Trumen measurements when Trumen changed between subsequent 3-minute measurement intervals by more than 0.25 °C. An integrated bi-axial acceleration sensor in the unit detected vibrations caused by the beating of the heart. Heart rate was calculated from the time intervals between two accelerations above an adaptive trigger level for measurement periods of 3 minutes. To extend battery life, the next 3-minute period of heart rate measurement was made after a pause of 18 minutes. Hence heart rate data were collected at 21-minute intervals. To save energy, the acceleration sensor was inactivated for 0.5 seconds upon acceleration above the trigger level. Therefore, the upper detectable limit of heart rate measurements was 120 beats per minute. We considered this limit as biologically meaningful because a higher heart rate is very unlikely to occur in a reindeer at rest or slow movement such as grazing. Data from the ruminal unit were sent via UHF-link to the collar unit and stored there in solid–state memory. For further details about the technology, see38.
Apart from contractions of the heart, movements of the animal and reticulum contractions also activated the acceleration sensor of the ruminal unit. Further, the UHF signal used for communication between the ruminal and collar unit was sometimes disturbed. Therefore, false measurements were removed from raw data after download with a stepwise software filter as follows:
Step 1: Removal of intervals with too few detectable heart beats. If the sum of time periods between accelerations above trigger level added up to less than 70% of 3 minutes, this 3-minute measurement interval of heart rate was discarded.
Step 2: Removal of data during locomotor activity. Activity was classified from the output of the triaxial vibration switch in the collar for each individual over the entire period of deployment of a telemetry system. The distribution of this output was always bimodal, typically with peaks very close to 0% and 100%. The lowest point of the distribution between the two modes was used as cut-off to classify each 3-minute measurement interval as spent active or inactive. All 3-minute measurement intervals of heart rate from active animals were discarded.
Step 3: Determination of the modal heart rate. For each of the remaining 3-minute measurement intervals, a Kernel density function was computed for the stored heart rate values, and the heart rate at maximum density was taken as the modal heart rate for this particular 3-minute interval.
Step 4: Removal of outliers. A spline curve (using function ‘gam’ in R) was fitted to the filtered heart rate data sampled over the entire period of deployment of a telemetry system. If the difference between values predicted from the spline fit (i.e. long-term trends in the data) and the modal heart rate within each 3-minute interval exceeded +30 or −20, this heart rate value was discarded.
In April 2012 four female reindeer from our marked population of ca. 400 individuals were caught by net from snowmobiles, measured, weighed to the nearest 0.5 kg38,39, and instrumented with the telemetry system (Table 1). Two of these four individuals (#1 and #3, both from the 2006 cohort) were re-captured the following April 2013. In April 2014 both these animals, together with #2 (2004 cohort) were re-captured and the collars were removed. Individual #4 (2009 cohort) was again missed but finally re-captured in April 2015 (see Table 1). Body mass is not available for years when individuals were not recaptured (NA in Table 1). Pregnancy status was assessed by ultrasound scans upon capture. Individuals #2 and #4 were observed during early August 2013 each with a calf on the heel. All procedures performed in this study were in accordance with relevant Norwegian regulations and guidelines. All capture and live animal handling procedures were performed under licences from the Norwegian Food Safety Authority and its predecessor the Norwegian Animal Research Authority (FOTS ID: 8417).
Quantification and statistical analysis
Raw data were downloaded from collars after retrieval. Obvious outliers beyond expected physiological limits typically occurred immediately after deploying telemetry devices and during periods before batteries died. Furthermore, Trumen of female #4 showed an unphysiological continuous decline after mid-November 2013, apparently due to a failure of the temperature sensor of the ruminal unit. These data were removed before applying the aforementioned filtering routines.
The beginning and end of summer periods with higher values were determined by fitting a special periodic regression model to empirical data, the so-called ‘baseline cosine function’. The baseline cosine function is an appropriate model to analyse rhythms that show temporal peaks above an otherwise largely stable baseline40. The parameters baseline, fraction of a cosine curve added to baseline to describe the peak, height of the sinusoidal peak above baseline, and acrophase of the rhythm were estimated for all variables measured with the R-function ‘nls’; 95% confidence intervals of the parameter estimates were determined with R-package ‘nlstools’41,42 to draw 95% confidence belts of the fits. Importantly, the function only delivers a baseline if its inclusion improves the fit compared to a complete cosine function40.
Searches for periodicities with period lengths between 30 minutes and 30 hours (to search for ultradian, diel and circadian rhythms), or 21 to 27 hours (to focus on diel and circadian rhythms), respectively, were performed with Lomb-Scargle periodogram analyses R-package ‘lomb’32. This method is superior to other statistical methods applied in biomedical rhythm research, including Fourier analysis, because it is particularly suited to detect periodic components in unequally sampled time-series, which includes data sets with missing values, but restricts all calculations to actually measured values32. Data obtained with loggers over longer periods of time typically have such features. For the Lomb-Scargle periodogram analyses we discarded data from individual #1 because the two months of valid measurements were too short.
We performed Lomb-Scargle periodogram analyses separately for periods with different light and vegetation conditions, i.e. the period when the sun is continuously below the horizon during winter (DD), the periods with daylight and night (LD), the period of continual light before the onset of the vegetation period with NDVI values <0 (LL low), and the period of continual light with above-ground live vascular plants (NDVI >0, LL high). Although we are aware that neither the Polar Night nor the Midnight Sun are conditions of truly constant illumination, we simply use the labels “DD” and “LL”, respectively, to enhance readability and retain standard chronobiologic terminology. For visualizing changes in periodicities over the year on a smaller scale, we further performed Lomb-Scargle periodogram analyses for subsequent intervals of 15 days, which exceeds the recommended minimum duration of ten periods for biological rhythm analyses31. The Lomb-Scargle periodogram provides the normalized power of each of the periods inspected. The term normalized refers to the fact that the raw power (i.e. the goodness-of-fit of the best period) is divided by twice the total variance in the time series (equation 1 in32). This normalization ensures that, in the case of the null hypothesis, the power follows an exponential distribution, which allows one to test whether the periodogram peak exceeds the level of statistical significance43. The probability of detecting a significant peak decreases with an increasing number of periods inspected, because this increases the probability of rhythms occurring by chance. Prior to computing periodograms, linear trends were removed from the time series.
The influence of environmental cues on diel rhythmicity of behaviour and physiology during the course of the year was tested with linear mixed modelling (R-package ‘nlme’44). We accounted for repeated measures by including individual identity as a random intercept factor into the models.
The datasets generated and analyzed during the current study are available at Dryad Digital Repository http://datadryad.org/.
Aschoff, J. Circadian Rhythms: Influences of Internal and External Factors on the Period Measured in Constant Conditions. Z Tierpsychol. 49, 225–249, https://doi.org/10.1111/j.1439-0310.1979.tb00290.x (1979).
Van der Wal, R. & Stien, A. High-arctic plants like it hot: a long-term investigation of between-year variability in plant biomass. Ecology 95, 3414–3427, https://doi.org/10.1890/14-0533.1 (2014).
Parker, K. L., Barboza, P. S. & Gillingham, M. P. Nutrition integrates environmental responses of ungulates. Funct. Ecol. 23, 57–69, https://doi.org/10.1111/j.1365-2435.2008.01528.x (2009).
Arnold, W. In Life in the Cold III: Ecological, Physiological, and Molecular Mechanisms (eds Carey, C., Florant, G. L., Wunder, B. A. & Horwitz, B.) 65–80 (Westview Press, 1993).
Williams, C. T., Barnes, B. M. & Buck, C. L. Persistence, Entrainment, and Function of Circadian Rhythms in Polar Vertebrates. Physiology 30, 86–96, https://doi.org/10.1152/physiol.00045.2014 (2015).
van Oort, B. E. H., Tyler, N. J. C., Gerkema, M. P., Folkow, L. & Stokkan, K.-A. Where clocks are redundant: weak circadian mechanisms in reindeer living under polar photic conditions. Naturwissenschaften 94, 183–194, https://doi.org/10.1007/s00114-006-0174-2 (2007).
van Oort, B. E. H. et al. Circadian organization in reindeer. Nature 438, 1095–1097, https://doi.org/10.1038/4381095a (2005).
Loe, L. E. et al. Activity pattern of arctic reindeer in a predator-free environment: no need to keep a daily rhythm. Oecologia 152, 617–624, https://doi.org/10.1007/s00442-007-0681-7 (2007).
Arnold, W., Ruf, T. & Kuntz, R. Seasonal adjustment of energy budget in a large wild mammal, the Przewalski horse (Equus ferus przewalskii) II. Energy expenditure. J Exp. Biol. 209, 4566–4573, https://doi.org/10.1242/jeb.02536 (2006).
Arnold, W. et al. Nocturnal hypometabolism as an overwintering strategy of red deer (Cervus elaphus). Am. J Physiol. Reg. Int. Comp. Physiol. 286, R174–R181, https://doi.org/10.1152/ajpregu.00593.2002 (2004).
Brinkmann, L., Gerken, M. & Riek, A. Adaptation strategies to seasonal changes in environmental conditions of a domesticated horse breed, the Shetland pony (Equus ferus caballus). J Exp. Biol. 215, 1061–1068, https://doi.org/10.1242/jeb.064832 (2012).
Signer, C., Ruf, T. & Arnold, W. Hypometabolism and basking: The strategies of Alpine ibex to endure harsh over-wintering conditions. Funct. Ecol. 25, 537–547, https://doi.org/10.1111/j.1365-2435.2010.01806.x (2011).
Turbill, C., Ruf, T., Mang, T. & Arnold, W. Regulation of heart rate and rumen temperature in red deer: effects of season and food intake. J Exp. Biol. 214, 963–970, https://doi.org/10.1242/jeb.052282 (2011).
Tyler, N. J. C. & Øritsland, N. A. Why don’t Svalbard reindeer migrate. Holarctic Ecol. 12, 369–376, https://doi.org/10.1111/j.1600-0587.1989.tb00911.x (1989).
Stien, A. et al. Icing events trigger range displacement in a high-arctic ungulate. Ecology 91, 915–920, https://doi.org/10.1890/09-0056.1 (2010).
Loe, L. E. et al. Behavioral buffering of extreme weather events in a high-Arctic herbivore. Ecosphere 7, e01374, https://doi.org/10.1002/ecs2.1374 (2016).
Côté, S. D. et al. Microsatellite DNA evidence for genetic drift and philopatry in Svalbard reindeer. Mol. Ecol. 11, 1923–1930, https://doi.org/10.1046/j.1365-294X.2002.01582.x (2002).
Heydon, M. J., Sibbald, A. M., Milne, J. A., Brinklow, B. R. & Loudon, A. S. I. The interaction of food availability and endogenous physiological cycles on the grazing ecology of red deer hinds (Cervus elaphus). Funct. Ecol. 7, 216–222, https://doi.org/10.2307/2389890 (1993).
Loudon, A. S. I. Photoperiod and the regulation of annual and circannual cycles of food intake. Proc. Nutr. Soc. 53, 495–507, https://doi.org/10.1079/PNS19940060 (1994).
Arnold, W. et al. Contrary seasonal changes of rates of nutrient uptake, organ mass, and voluntary food intake in red deer (Cervus elaphus). Am. J Physiol. Reg. Int. Comp. Physiol. 309, R277–R285, https://doi.org/10.1152/ajpregu.00084.2015 (2015).
Pohl, H. Temperature Cycles as Zeitgeber for the Circadian Clock of Two Burrowing Rodents, the Normothermic Antelope Ground Squirrel and the Heterothermic Syrian Hamster. Biol. Rhythm Res. 29, 311–325, https://doi.org/10.1076/brhm.29.3.311.1436 (1998).
Rani, S. & Kumar, V. Phasic response of the photoperiodic clock to wavelength and intensity of light in the redheaded bunting. Emberiza bruniceps. Physiol. Behav. 69, 277–283, https://doi.org/10.1016/S0031-9384(99)00247-4 (2000).
Malik, S., Rani, S. & Kumar, V. Wavelength Dependency of Light-Induced Effects on Photoperiodic Clock in the Migratory Blackheaded Bunting (Emberiza melanocephala). Chronobiol. Int. 21, 367–384, https://doi.org/10.1081/Cbi-120038742 (2004).
Pauers, M. J., Kuchenbecker, J. A., Neitz, M. & Neitz, J. Changes in the colour of light cue circadian activity. Anim. Behav. 83, 1143–1151, https://doi.org/10.1016/j.anbehav.2012.01.035 (2012).
Ashley, N. T., Schwabl, I., Goymann, W. & Buck, C. L. Keeping Time Under the Midnight Sun: Behavioral and Plasma Melatonin Profiles of Free-Living Lapland Longspurs (Calcarius lapponicus) During the Arctic Summer. J Exp. Zool. A 319, 10–22, https://doi.org/10.1002/jez.1768 (2013).
Ashley, N. T. et al. Revealing a Circadian Clock in Captive Arctic-Breeding Songbirds, Lapland Longspurs (Calcarius lapponicus), under Constant Illumination. J Biol. Rhythms 29, 456–469, https://doi.org/10.1177/0748730414552323 (2014).
Wever, R. A. The Circadian System of Man. Results of Experiments Under Temporal Isolation (Springer, 1979).
Daan, S., Honma, S. & Honma, K. Body temperature predicts the direction of internal desynchronization in humans isolated from time cues. J Biol. Rhythms 28, 403–411, https://doi.org/10.1177/0748730413514357 (2013).
Pittendrigh, C. S. & Daan, S. A Functional Analysis of Circadian Pacemakers in Nocturnal Rodents. I. The Stability and Lability of Spontaneous Frequency. J Comp. Physiol. A 106, 223–252, https://doi.org/10.1007/BF01417856 (1976).
Kuntz, R., Kubalek, C., Ruf, T., Tataruch, F. & Arnold, W. Seasonal adjustment of energy budget in a large wild mammal, the Przewalski horse (Equus ferus przewalskii) I. Energy intake. J Exp. Biol. 209, 4557–4565, https://doi.org/10.1242/jeb.02535 (2006).
Sokolove, P. G. & Bushell, W. N. The Chi Square Periodogram: Its Utility for Analysis of Circadian Rhythms. J Theor. Biol. 72, 131–160, https://doi.org/10.1016/0022-5193(78)90022-X (1978).
Ruf, T. The Lomb-Scargle Periodogram in Biological Rhythm Research: Analysis of incomplete and unequally spaced time-series. Biol. Rhythm Res. 30, 178–201, https://doi.org/10.1076/brhm.220.127.116.112 (1999).
Lu, W., Meng, Q.-J., Tyler, N. J. C., Stokkan, K.-A. & Loudon, A. S. I. A Circadian Clock Is Not Required in an Arctic Mammal. Curr. Biol. 20, 533–537, https://doi.org/10.1016/j.cub.2010.01.042 (2010).
Van der Wal, R. & Brooker, R. W. Mosses mediate grazer impacts on grass abundance in arctic ecosystems. Funct. Ecol. 18, 77–86, https://doi.org/10.1111/j.1365-2435.2004.00820.x (2004).
Albon, S. D. et al. Contrasting effects of summer and winter warming on body mass explain population dynamics in a food-limited Arctic herbivore. Global Change Biol. 23, 1374–1389, https://doi.org/10.1111/gcb.13435 (2017).
Larter, N. C. & Nagy, J. A. Variation between snow conditions at Peary caribou and muskox feeding sites and elsewhere in foraging habitats on banks island in the Canadian High Arctic. Arct. Antarct. Alp. Res. 33, 123–130, https://doi.org/10.2307/1552212 (2001).
Gionata, B. R. Atmosphere: Standard Atmospheric profiles (R package version1.1.), https://CRAN.R-project.org/package=RAtmosphere (2014).
Signer, C. et al. A versatile telemetry system for continuous measurement of heart rate, body temperature and locomotor activity in free-ranging ruminants. Methods Ecol. Evol. 1, 75–85, https://doi.org/10.1111/j.2041-210X.2009.00010.x (2010).
Ropstad, E. et al. Comparison of Plasma Progesterone, Transrectal Ultrasound and Pregnancy Specific Proteins (PSPB) used for Pregnancy Diagnosis in Reindeer. Acta Vet. Scand. 40, 151–162 (1999).
Ruf, T. The Baseline Cosinus Function: a Periodic Regression Model for Biological Rhythms. Biol. Rhythm Res. 27, 153–165, https://doi.org/10.1076/brhm.18.104.22.16842 (1996).
R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria, http://www.R-project.org/ (R Foundation for Statistical Computing, Vienna, Austria, 2016).
Baty, F. et al. A Toolbox for Nonlinear Regression in R: The Package nlstools. J Stat. Softw. 66, 1–21, https://doi.org/10.18637/jss.v066.i05 (2015).
Scargle, J. D. Studies in astronomical time series analysis. II. Statistical aspects of spectral analysis of unevenly spaced data. The Astrophysical Journal 263, 835–853, https://doi.org/10.1086/160554 (1982).
Pinheiro, J., Bates, D., DebRoy, S. & Sarkar, D. R Core Team. nlme: Linear and Nonlinear Mixed Effects Models (R package version 3.1–128), http://CRAN.R-project.org/package=nlme (2016).
Brainard, G. C., Richardson, B. A., King, T. S., Matthews, S. A. & Reiter, R. J. The Suppression of Pineal Melatonin Content and N-AcetyItransferase Activity by Different Light Irradiances in the Syrian Hamster: A Dose-Response Relationship. Endocrinology 113, 293–296, https://doi.org/10.1210/endo-113-1-293 (1983).
Dedication in memoriam Prof. Dr. Serge Daan (1940-2018), one of the greatest thinkers in Chronobiology. We thank the Governor of Svalbard for permission to undertake the research on Svalbard reindeer. We are especially grateful to Steve Coulson, and the logistical and technical staff at the University Centre in Svalbard (UNIS) for supporting the field campaigns between 2012 and 2015. We thank Renate Hengsberger for help with manuscript submission. The on-going study was financed by the Research Council of Norway (RCN: Centre of Excellence project 223257 to Bert-Erik Sæther, and KLIMAFORSK project 244647 to Brage Hansen). The specific radio collars and rumen boluses were funded by a Macaulay Development Trust grant to Steve Albon. Additional financial support during this specific study period (2012–2015) came from The James Hutton Institute (Steve Albon and R. Justin Irvine), the Norwegian Institute for Nature Research (Vebjørn Veiberg), UNIS for equipment and logistics, and the Norwegian University of Life Sciences (Leif Egil Loe and Erik Ropstad).
The authors declare no competing interests.
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Arnold, W., Ruf, T., Loe, L.E. et al. Circadian rhythmicity persists through the Polar night and midnight sun in Svalbard reindeer. Sci Rep 8, 14466 (2018). https://doi.org/10.1038/s41598-018-32778-4
- Polar Night
- Svalbard Reindeer
- Lomb-Scargle Periodogram Analysis
- Diel Rhythmicity
- Continuous Daylight
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