Habitat displacement effect between two competing owl species in fragmented forests

Many owl species use the same nesting and food resources, which causes strong interspecific competition and spatio-temporal niche separation. We made use of a recent colonisation of Ural Owls (Strix uralensis) in southern Poland to compare habitat preferences of Tawny Owls (Strix aluco) allopatry and sympatry with Ural Owls. We investigated spatial niche segregation of Ural Owl and the Tawny Owl in sympatry and compared habitat preferences of Tawny Owls breeding in allopatry and sympatry. Tawny Owls breeding in sympatry with Ural Owls occupied forests with higher canopy compactness, sites located closer to forest border and to built-up areas, as well as stands with a higher share of fir and spruce and a lower share of beech as compared to sites occupied by Ural Owls. Allopatric Tawny Owls occupied sites with lower canopy compactness and bred at sites located further from forest borders and in stands with lower share of fir and spruce and a higher share of deciduous as compared to sympatric Tawny Owls. As Ural owls are dominant in relation to Tawny Owls, this indicates that the presence of Ural Owls prevents Tawny Owls from occupying deciduous-dominated and old stands located in forest interior areas, far from buildings and forest edges. The results support habitat displacement between the two species when breeding in sympatry. We also show that protection of large forest patches is crucial for the Ural Owl, a species still rare in central Europe, while small patches are occupied by the abundant Tawny Owl.     

Noise pollution and decreased size of wooded areas reduces the probability of occurrence of Tawny Owl Strix aluco

At present, urban areas cover almost 3% of the Earth's land surface, and this proportion is constantly increasing along with human population growth. Although urbanization leads to biodiversity decline, at the same time it creates a novel and extensive environment that is exploited by whole assemblages of organisms. These include predators, which use the matrix of different habitat types within the urban environment for breeding and/or foraging. This study investigated how attributes of the urban landscape influence the distribution pattern of a nocturnal acoustic predator, the Tawny Owl Strix aluco. The probability of occurrence of this species was correlated with the presence of natural forests, and the increasing size of wooded habitat patches within the urban landscape; however, Tawny Owls were less likely to occur at sites with high noise levels at night. Our study suggests that the distribution pattern of acoustic predators is shaped by the availability of primary habitat but reduced by noise intensity (which may decrease hunting efficiency). The Tawny Owl is a top predator in the urban environment and its presence/absence may therefore affect populations of other species; this provides clear evidence of the indirect effect of noise pollution on animal populations inhabiting urban environments.     

Altitudinal segregation between Ural Owl Strix uralensis and Tawny Owl S. aluco: evidence for competitive exclusion in raptorial birds

Capsule The Owls were significantly segregated in space with the most important factor being altitude.

Aims To establish if the segregation between Ural and Tawny Owl on the level of habitat selection is due to different habitat requirements of the species or a consequence of competitive exclusion.

Methods Seven variables were recorded for habitat of Ural Owls, Tawny Owls that live in sympatry with Ural Owls and Tawny Owls that live in allopatry with Ural Owls. Data were gathered in five mountain areas covered with similar continuous montane forest inside and outside known Ural Owl distribution in Slovenia. Owl territories were surveyed in 2001 using playback method. Evidence for segregation was searched for using discriminant function analysis.

Results The altitudinal distribution of Tawny Owls sympatric to Ural Owls was restricted to low elevations with Ural Owls at high elevations. Where Ural Owls were absent, Tawny Owls widened the altitudinal part of their ecological niche to the mountaintop.

Conclusion Segregation between Tawny and Ural Owls is due to competitive exclusion, with the less competitive Tawny Owl being out-competed by the superior Ural Owl. The forests at foothills are influenced by human presence and therefore avoided by Ural Owls. In areas where both species live in sympatry, these areas act as refugia for Tawny Owls.     

Environmental correlates of annual survival differ between two ecologically similar and congeneric owls

Understanding how survival is affected by the environment is essential to gain insight into population dynamics and the evolution of life‐history traits as well as to identify environmental selection pressures. However, we still have little understanding of the relative effect of different environmental factors and their interactions on demographic traits and population dynamics. Here we used two long‐term, individual‐based datasets on Tawny Owl Strix aluco (1981–2010) and Ural Owl S. uralensis (1986–2010) to undertake capture‐mark‐recapture analysis of annual survival of adult females in response to three biologically meaningful environmental variables and their two‐way interactions. Despite the similar ecology of these two species, their survival was associated with different and uncorrelated environmental drivers. The main correlate of Tawny Owl survival was an inverse association with snow depth (winter severity). For Ural Owl, high food (vole) abundance improved survival during years with deep snow, but was less important during years with little snow. In addition, Ural Owl survival was strongly density‐dependent, whereas Tawny Owl survival was not. Our findings advise caution in extrapolating demographic inferences from one species to another, even when they are very closely related and ecologically similar. Analyses including only one or few potential environmental drivers of a species' survival may lead to incomplete conclusions because survival may be affected by several factors and their interactions.     

The impact of predation by birds on bat populations in the British Isles

The role played by predation of birds in the mortality of British bats is assessed. A review of dietary studies and anecdotal accounts revealed eleven species of bird which occasionally feed on bats–Herring Gull Larus argentatus , Black-headed Gull Larus ridibundus , Rook Corvus frugilegus , Carrion Crow Corvus corone , Little Owl Athene noctua , Short-eared Owl Asio flammeus , Kestrel Falco tinnunculus , Hobby Falco subbuteo , Merlin Falco columbarius , Peregrine Falco peregrinus and Sparrowhawk Accipiter nisus. A further three species feed more frequently on bats–Barn Owl Tyto alba , Tawny Owl Strix aluco and Long-eared Owl Asio otus. Rates of predation were very low accounting for only 00034^o_o of items taken by small hawks and falcons ( n items = 29 519) but 0035^o, of prey taken by owls ( n items = 99 479). By multiplying together the average annual prey capture rates of the predators, assessed from their energetic food requirements and direct observations of prey intake rates, the British populations of the predators and the contribution to the diet made by bats, the annual number of bats which die each year as a result of predation was estimated. The total losses of bats to predation might amount to about 201 400 bats/annum. The most significant predators are Tawny Owl ( c. 168 850 bats/annum), Barn Owl (c. 8800 bats/ annum), Long-eared Owl (c. 10 200 bats/annum) and Kestrels (c. 8400 bats/annum). This predation by avian predators would account for about 11 % of the annual mortality of British bats. An assessment of the biases involved in this calculation suggests it is probably a minimum estimate. Despite the apparent low representation of bats in the diets of predatory birds, the effects of this predation on bat behaviour and population dynamics cannot be ignored.     

A comparison of three methods for planning a census of Tawny Owl (Strix aluco) populations living at high territorial density

Censusing nocturnal species such as the Tawny Owl (Strix aluco) living in a dense population can lead to an overestimate if individual signatures are not available. A technique that separates the individualistic call of the Tawny Owl could be a useful tool for an exhaustive census. Six Tawny Owl males were followed for nine months; 654 vocalizations were analysed. Three methods – Spectrographic Cross Correlation (SPCC), Acoustic Space (AS) and Visual Spectrogram Comparison (VSC) – were tested to assess their ability to classify the typical male call. For SPCC, 10 randomly selected hoots for each male were compared: the distributions of correlation coefficients differed in only 26.7% of the cases when intra and inter individual variability are compared. For AS, all the spectrograms were measured through 13 parameters and intra and inter individual distances were compared: the interval containing 95.4% of intra-individual measures also contained 95.9% of inter-individual comparisons. Both SPCC and AS are considered not to be able to adequately separate subjects. For VSC, 31 randomly selected hoots were visually compared by 5 helpers; their classifications were compared pairwise and with the real situation; operators correctly identified a male in 70% of cases (mean = 70.4 SD = 5.4). If we integrate VSC with information coming from field notes, we have a more powerful tool than the mapping method. It is plausible that this technique can be useful for an exhaustive census of Tawny Owl populations living at high densities.     

Temperature effects on low-light vision in juvenile rockfish (Genus <Emphasis Type="Italic">Sebastes</Emphasis>) and consequences for habitat utilization

The absolute low-light sensitivity of four congeneric species of rockfish (genus Sebastes) was studied from analysis of electroretinograms measured in living fish. The purpose was: (1) to determine if temperature sensitive noise in rod photoreceptors affects the absolute limit to low-light sensitivity at environmentally realistic temperatures and light levels, and (2) to examine whether interspecific variations in habitat utilization within rockfish communities correlate with differences in visual sensitivity. It was found that the low-light sensitivity of individual retinae is inversely dependent on temperature, decreasing tenfold with a 10°C increase in temperature. While in all four species, temperature had a similar effect on sensitivity, the absolute sensitivity levels were different. The four species could be divided into two groups based on measured sensitivity. Kelp and olive rockfish form a high-sensitivity group capable of responding to light levels approximately 50-fold lower than blue and black rockfish. The sensitivity groups correlated with reported diel activity patterns; the high-sensitivity group forages nocturnally, whereas members of the low-sensitivity group are quiescent during twilight and night and forage during the day.     

The costs of becoming nocturnal: feeding efficiency in relation to light intensity in juvenile Atlantic Salmon

1. Most animals are active by day or by night, but not both; juvenile salmonids are unusual in that they switch from being predominantly diurnal for most of the year to being nocturnal in winter. They are visual foragers, and adaptations for high visual acuity at daytime light intensities are generally incompatible with sensitive night vision. Here we test whether juvenile Atlantic Salmon Salmo salar are able to maintain their efficiency of prey capture when switching between diurnal and nocturnal foraging.
2. By testing the ability of the fish to acquire drifting food items under a range of manipulated light intensities, we show that the foraging efficiency of juvenile salmon is high at light intensities down to those equivalent to dawn or dusk, but drops markedly at lower levels of illumination: even under the best night condition (full moon and clear sky), the feeding efficiency is only 35% of their diurnal efficiency, and fish will usually be feeding at less than 10% (whenever the moon is not full, skies are overcast or when in the shade of bankside trees). Fish were unable to feed on drifting prey when in complete darkness.
3. The ability of juvenile salmon to detect prey under different light intensities is similar to that of other planktivorous or drift-feeding species of fish; they thus appear to have no special adaptations for nocturnal foraging.
4. While winter drift abundance is slightly higher by night than by day, the difference is not enough to compensate for the loss in foraging efficiency. We suggest that juvenile salmon can nonetheless switch to nocturnal foraging in winter because their food requirements are low, many individuals adopting a strategy in which intake is suppressed to the minimum that ensures survival.     

Movement and direction of movement of a simulated prey affect the success rate in barn owl Tyto alba attack

The present study was aimed at testing a novel idea, that rather than maximizing their distance from a predator during close-distance encounters, prey species are better off moving directly or diagonally toward the predator in order to increase the relative speed and confine the attack to a single available clashing point. We used two tamed barn owls Tyto alba to measure the rate of attack success in relation to the direction of prey movement. A dead mouse or chick was used to simulate the prey, pulled to various directions by means of a transparent string during the owl's attack. Both owls showed a high success rate in catching stationary compared with moving food items (90% and 21%, respectively). Success was higher when the prey moved directly away, rather than towards the owls (50% and 18%, respectively). Strikingly, these owls had 0% success in catching food items that were pulled sideways. This failure to catch prey that move sideways may reflect constraints in postural head movements in aerial raptors that cannot move the eyes but rather move the entire head in tracking prey. So far there is no evidence that defensive behavior in terrestrial prey species takes advantage of the above escape directions to lower rates of predator success. However, birds seem to adjust their defensive tactics in the vertical domain by taking-off at a steep angle, thus moving diagonally toward the direction of an approaching aerial predator. These preliminary findings warrant further studies in barn owls and other predators, in both field and laboratory settings, to uncover fine predator head movements during hunting, the corresponding defensive behavior of the prey, and the adaptive significance of these behaviors.     

浙江千岛湖黄腿渔鸮的繁殖记录

<正>黄腿渔鸮(Ketupa flavipes)隶属于鸮形目鸱鸮科,1836年由英国博物学家Brian Houghton Hodgson在尼泊尔发现并命名。为单型种,无亚种分化。分布范围从喜马拉雅山脉延伸至中南半岛东部、中国大陆中南部及台湾,我国主要见于东部、中部和南部。在云南、贵州、四川、重庆、湖北、湖南、安徽、江西、江苏、上海、浙江、福建、广东、广西和台湾等地有记录(郑光美2011),均为留鸟。黄腿渔鸮为我国国家Ⅱ级重点保护动物;在IUCN     

PREY TAKEN BY TAWNY OWLS DURING THE BREEDING SEASON

The diet of Tawny Owls during the breeding seasons 1949-52 in Wytham Woods, near Oxford, was determined (a) from analysis of pellets collected, (b) from observation at night, by the use of a red floodlight, of prey brought to the nest and (c) from records of prey left in the nest made during daily visits to weigh the young.
Analysis of pellets showed an increase in the proportion of moles and beetles (mainly cockchafen) in the diet after the first week of May (the time when, on average, the young owls are about half grown) and a decrease in the proportion of mice and voles.
These changes were confirmed in a more emphatic way from observations of food being brought to the nest and from records of prey left in the nest.
This greater emphasis suggests that tho food brought to the young may differ from that which the adults eat themselves.
The fact that no moles were observed being brought to nests at night, wherean many were recorded as surplus prey in the nest, showed that diurnal hunting is regular during the breeding reaaon.
A true assessment of prey taken by Tawny Owls during the breeding season should be based both on analyeis of pellets cast by the adults and on records of food brought to the nest throughout 24 hours. Such records could best be obtained with an automatic camera and flash and a design of nest-box which is described.     

北京门头沟灰林鸮繁殖记录

<正>灰林鸮(Strix aluco)是广泛分布于欧亚大陆及非洲西北部温暖森林地带的鸮形目(Strigiformes)鸱鸮科(Strigidae)猛禽(del Hoyo et al.1999)。2008年出版的鸮形目鸟类专著Owls of the World将分布于南亚、东亚、东南亚的原属Strix aluco的种群划分出来作为一个独立的种Strix nivicola(K?nig et al.2008),其英文名为     

Light intensity, prey detection and foraging mechanisms of age 0 year yellow perch

The ability of age‐0 year yellow perch Perca flavescans to detect prey using visual and mechano‐sensory input was examined during laboratory feeding trials at varying light intensities. Perch were highly effective predators and captured Daphnia pulicaria with 94% overall foraging success at light levels ranging from 0 to 3400 lx. Maximum average reaction distances (5·0 ± 0·8 cm, mean ±  s . e .) occurred in front of the fish at 3000 lx and significantly decreased as light intensities fell to <2 lx, with minimum reaction distances (2·8 ± 0·1 cm) observed in the dark. Following chemical ablation of the lateral line, yellow perch showed a significant reduction in reaction distance when compared to the untreated fish at 3000 lx, suggesting that the lateral line may augment visual prey detection at high light levels. A model was created to predict reaction distances for fish feeding with multiple sensory systems that can be applied to a variety of photic environments. This study provides a better understanding of the contribution of vision and the lateral line to prey detection, and relates the reaction distance of age‐0 year yellow perch to light intensities similar to those experienced in nature.     

Prey selection and foraging constraints in common poorwills (Phalaenoptilus nuttallii: Aves: Caprimulgidae)

Predators that hunt by sight should be constrained by light levels. This problem should be especially acute in aerial predators such as common poorwills ( Phalaenoptilus nuttallii : Caprimulgidae), which capture small insects at night. The purpose of our study was to test the hypothesis that poorwills are constrained to catching larger insect taxa due to limitations of visual orientation under low light. We assessed diet by analysing poorwill faecal samples collected at nest and roost sites in the Cypress Hills of Saskatchewan where prey density is relatively low. Coleopterans (44% and 39% in 1991 and 1992, respectively) and lepidopterans (46% and 55%) dominated the diet, yet these two insect orders were rare in light-suction trap (22% lepidopterans and 1% coleopterans) and sticky trap samples (11% lepidopterans and 2% coleopterans). Based on measurements of femur length, all consumed coleopterans were > 5 mm long, even though 57% of those available were < 5 mm. Our results suggest that poorwills are constrained to taking prey above a certain size, but above this threshold, particular prey types and larger sizes may be selected. Selection for coleopterans may reflect the need to acquire polyunsaturated fat to facilitate the use of torpor.     

Fishing in the dark: a pursuit-diving seabird modifies foraging behaviour in response to nocturnal light levels

Visual predators tend not to hunt during periods when efficiency is compromised by low light levels. Yet common murres, a species considered a diurnal visual predator, frequently dive at night. To study foraging of murres under different light conditions, we used a combination of archival tagging methods and astronomical models to assess relationships between diving behaviour and light availability. During diurnal and crepuscular periods, murres used a wide range of the water column (2-177 m), foraging across light intensities that spanned several orders of magnitude (10(3)-10(-10) Wm(-2)). Through these periods, they readily dived under conditions equivalent to ambient moonlight (~10(-4) Wm(-2)) but rarely under conditions equivalent to starlight (~10(-8) Wm(-2)). At night, murres readily foraged during both moonlit and starlit periods, and diving depth and efficiency increased with nocturnal light intensity, suggesting that night diving is at least partially visually guided. Whether visually guided foraging is possible during starlit periods is less clear. Given the dense prey landscape available, random-walk simulations suggest that murres could benefit from random prey encounters. We hypothesise that murres foraging through starlit periods rely either on close-range visual or possibly nonvisual cues to acquire randomly encountered prey. This research highlights the flexibility of breeding common murres and raises questions about the strategies and mechanisms birds use to find prey under very low light conditions.     

Experimental analysis of the prey catching behavior ofHydromantes italicus Dunn (Amphibia,Plethodontidae)

Summary 1. The Italian bolitoglossine salamanderHydromantes italicus shows a periodic cave life. In spring and in the fall it leaves the caves after which it lives under stones, in leaves and crevices. Inside the limestone caves,H. i. can be found both in the zone of dim light near the entrance and in total darkness. 2. Corresponding to these two environments there are two guidance systems of the prey catching behavior: one visual and one olfactory. 3. The visually guided prey catching behavior is determined by the stimulus parameters: velocity, size, contrast, and ambient illumination. Continuously moving objects are effective within a velocity range of 0.05 to 6 cm/s with an optimum at 1.25 cm/s (Fig. 2). Stimuli moving stepwise elicit fixation of the prey and complete approach more frequently than continuously moving stimuli. The prey size which elicits prey catching ranges from 0.5 to 10 mm² with an optimum size between 2.5–5.0 mm² (Fig. 3). The prey catching behavior is hardly impaired by a decrease in ambient illumination down to 0.03 cd/m². Beyond 0.03 cd/m², the prey catching activity decreases sharply, but there are still responses at an illumination level of 0.003 cd/m² (Fig. 4). 4.H.i. also responds to stationary non-smelling visual stimuli following stimulation by smell or movement.H.i. is able to detect prey by smell only both in total darkness and in the light (Fig. 5 A). In the light, the prey catching behavior with regard to smelling objects is inhibited by the absence of visual contrast (Fig. 5B).I would like to thank Prof. Dr. R. Altevogt, University of Münster (Germany) for his generous help and constant encouragement. Furthermore, I want to express my gratitude to Prof. Dr. D.B. Wake, University of California, Berkeley (USA), Prof. Dr. P. Mancino, University of Pisa (Italy), and Prof. Dr. J.-P. Ewert, University (GH) of Kassel (Germany) for stimulating discussions and helpful comments.     

Piscivore-Prey Fish Interactions: Mechanisms behind Diurnal Patterns in Prey Selectivity in Brown and Clear Water

Environmental change may affect predator-prey interactions in lakes through deterioration of visual conditions affecting foraging success of visually oriented predators. Environmental change in lakes includes an increase in humic matter causing browner water and reduced visibility, affecting the behavioural performance of both piscivores and prey. We studied diurnal patterns of prey selection in piscivorous pikeperch (Sander lucioperca) in both field and laboratory investigations. In the field we estimated prey selectivity and prey availability during day and night in a clear and a brown water lake. Further, prey selectivity during day and night conditions was studied in the laboratory where we manipulated optical conditions (humic matter content) of the water. Here, we also studied the behaviours of piscivores and prey, focusing on foraging-cycle stages such as number of interests and attacks by the pikeperch as well as the escape distance of the prey fish species. Analyses of gut contents from the field study showed that pikeperch selected perch (Perca fluviatilis) over roach (Rutilus rutilus) prey in both lakes during the day, but changed selectivity towards roach in both lakes at night. These results were corroborated in the selectivity experiments along a brown-water gradient in day and night light conditions. However, a change in selectivity from perch to roach was observed when the optical condition was heavily degraded, from either brown-stained water or light intensity. At longer visual ranges, roach initiated escape at distances greater than pikeperch attack distances, whereas perch stayed inactive making pikeperch approach and attack at the closest range possible. Roach anti-predatory behaviour decreased in deteriorated visual conditions, altering selectivity patterns. Our results highlight the importance of investigating both predator and prey responses to visibility conditions in order to understand the effects of degrading optical conditions on piscivore-prey interaction strength and thereby ecosystem responses to brownification of waters.     

Tawny Owl Strix aluco as an indicator of Barn Owl Tyto alba breeding biology and the effect of winter severity on Barn Owl reproduction

In the temperate zone, food availability and winter weather place serious constraints on European Barn Owl Tyto alba populations. Using data collected over 22 years in a Swiss population, we analysed the influence of early pre‐breeding food conditions and winter severity on between‐year variations in population size and reproductive performance. To estimate pre‐breeding food conditions, we attempted a novel approach based on an index that combines Tawny Owl Strix aluco reproductive parameters and the occurrence of wood mice Apodemus sp. in their diet. Tawny Owls breed earlier in the season than Barn Owls and are strongly dependent on the abundance of wood mice for breeding. This index was strongly positively associated with the number of breeding pairs and early breeding in the Barn Owl. Winter severity, measured by snow cover and low temperatures, had a pronounced negative influence on the size of the breeding population and clutch size. Food conditions early in the breeding season and winter severity differentially affect the Barn Owl life cycle. We were able to use aspects of the ecology and demography of the Tawny Owl as an indicator of the quality of the environment for a related species of similar ecology, in this case the Barn Owl.     

Detection of earthworm prey by Ruff Philomachus pugnax

Ruff Philomachus pugnax staging in the Netherlands forage in agricultural grasslands, where they mainly eat earthworms (Lumbricidae). Food intake and the surface availability of earthworms were studied in dairy farmland of southwest Friesland in March–April 2011. Daily changes in earthworm availability were quantified by counting visible earthworms. No earthworms were seen on the surface during daytime, but their numbers sharply increased after sunset and remained high during the night. Nevertheless, intake rates of individual Ruff in different grasslands measured during daytime showed the typical Holling type II functional response relationship with the surfacing earthworm densities measured at night. Radiotagging of Ruff in spring 2007 revealed that most, if not all, feeding occurs during the day, with the Ruff assembling at shoreline roosts at night. This raises the question of why Ruff do not feed at night, if prey can be caught more easily than during daytime. In March–May 2013 we experimentally examined the visual and auditory sensory modalities used by Ruff to find and capture earthworms. Five males were kept in an indoor aviary and we recorded them individually foraging on trays with 10 earthworms mixed with soil under various standardized light and white noise conditions. The number of earthworms discovered and eaten by Ruff increased with light level, but only when white noise was played, suggesting that although they can detect earthworms by sight, Ruff also use auditory cues. We suggest that although surfacing numbers of earthworms are highest during the night, diurnal intake rates are probably sufficient to avoid nocturnal foraging on a resource that is more available but perhaps less detectable at that time.     

Is Ambient Light during the High Arctic Polar Night Sufficient to Act as a Visual Cue for Zooplankton?

The light regime is an ecologically important factor in pelagic habitats, influencing a range of biological processes. However, the availability and importance of light to these processes in high Arctic zooplankton communities during periods of ''complete'' darkness (polar night) are poorly studied. Here we characterized the ambient light regime throughout the diel cycle during the high Arctic polar night, and ask whether visual systems of Arctic zooplankton can detect the low levels of irradiance available at this time. To this end, light measurements with a purpose-built irradiance sensor and coupled all-sky digital photographs were used to characterize diel skylight irradiance patterns over 24 hours at 79°N in January 2014 and 2015. Subsequent skylight spectral irradiance and in-water optical property measurements were used to model the underwater light field as a function of depth, which was then weighted by the electrophysiologically determined visual spectral sensitivity of a dominant high Arctic zooplankter, Thysanoessa inermis. Irradiance in air ranged between 1–1.5 x 10^-5 μmol photons m^-2 s^-1 (400–700 nm) in clear weather conditions at noon and with the moon below the horizon, hence values reflect only solar illumination. Radiative transfer modelling generated underwater light fields with peak transmission at blue-green wavelengths, with a 465 nm transmission maximum in shallow water shifting to 485 nm with depth. To the eye of a zooplankter, light from the surface to 75 m exhibits a maximum at 485 nm, with longer wavelengths (>600 nm) being of little visual significance. Our data are the first quantitative characterisation, including absolute intensities, spectral composition and photoperiod of biologically relevant solar ambient light in the high Arctic during the polar night, and indicate that some species of Arctic zooplankton are able to detect and utilize ambient light down to 20–30m depth during the Arctic polar night.