Search

The Arctic fox (Vulpes lagopus), occupying tundra habitats with highly variable resource distribution, is a convenient research model for studying the impact of food availability on space use. Previous studies have shown that the Arctic fox home ranges can vary from 4 to 125 km2. In areas with abundant food resources, home range sizes are smaller and overlap increases. It is theoretically assumed that with an excess of resources, territoriality should disappear. We investigated a fox settlement at the Northern fur seal rookery on Bering Island (North Pacific). We used GPS collars to track nine foxes in the summer of 2014 and 2016. GPS locations were recorded at 5-min intervals. In the home range estimation, we used the Brownian bridge movement model. We also calculated home range sizes using 100% minimum convex polygon (MCP100) and 95% fixed kernel methods to compare our results with previous studies. Home ranges were extremely small with an average of 0.5 km2 (range of 0.2–0.9 km2) by Brownian Bridge and 0.7 km2 (0.3–1.4 km2) by MCP100. We revealed no sex differences in home range size but discovered strong differentiation of activity spatial concentration between males and females. We found a surprisingly small overlap between neighboring foxes, reflecting high territoriality. This runs counter to the trend expected with an overabundant food source. We assume that the combination of the super small size of the home ranges and their exclusivity may be a feature of the island fox land tenure system, which prevents inbreeding and deters infanticide.

This is a pre-print of an article published in Oecologia. The final authenticated version is available online at: https://doi.org/10.1007/s00442-019-04580-0 Identifying resources driving long-term trends in predators is important to understand ecosystem changes and to manage populations in the context of conservation or control. The arctic fox population in Iceland has increased steadily over a period of 30 years, an increase that has been attributed to an overall increase in food abundance. We hypothesized that increasing populations of geese or seabirds were driving this growth. We analyzed stable isotopes in a long-term series of collagen samples to determine the role of these different resources. The isotopic signatures of arctic foxes differed consistently between coastal and inland habitats. While δ15N displayed a non-linear change over time with a slight increase in the first part of the period followed by a decline in both habitats, δ13C was stable. Stable isotope mixing models suggested that marine resources and rock ptarmigan were the most important dietary sources, with marine resources dominating in coastal habitats and rock ptarmigan being more important inland. Our results suggest that seabirds may have been driving the arctic fox population increase. The rapidly increasing populations of breeding geese seem to have played a minor role in arctic fox population growth, as rock ptarmigan was the most important terrestrial resource despite a considerable decrease in their abundance during recent decades. This study shows that a long-term population trend in a generalist predator may have occurred without a pronounced change in main dietary resources, despite ongoing structural changes in the food web, where one species of herbivorous birds increased and another decreased.

Lengths, widths, and size proportions (length to width) of the lower carnassial were measured in 45 teeth of the arctic fox and 35 teeth of the red fox from Belgium radiocarbon dated to 46 640–14 120 ka BP. Data the Late Pleistocene foxes from Belgium were compared to 20 ancient and extant populations form Europe, Asia, and North America. The Pleistocene arctic fox from Belgium showed larger carnassial than in all recent samples of this species, whereas the Belgian fossil red foxes were characterized by the carnassial size comparable to that of the recent Siberian red foxes. Both fox species from the Pleistocene of Belgium showed the highest index of the carnassials length to width, which means increase in carnivorous adaptation. We conclude that the higher level of carnivorous specialization reached by the Belgian arctic and red foxes at the end of the Late Pleistocene reflected their scavenging on kills of large carnivores and human hunters (remains of megafauna). Harsh environmental conditions of that period and specific composition of ecosystems led to adapting to a more carnivorous food niche in both foxes.

The arctic fox (Vulpes lagopus), an apex predator with an omnipresent distribution in the Arctic, is a potential source of intestinal parasites that may endanger people and pet animals such as dogs, thus posing a health risk. Non-invasive methods, such as coprology, are often the only option when studying wildlife parasitic fauna. However, the detection and identification of parasites are significantly enhanced when used in combination with methods of molecular biology. Using both approaches, we identified unicellular and multicellular parasites in faeces of arctic foxes and carcasses of sibling voles (Microtus levis) in Svalbard, where molecular methods are used for the first time. Six new species were detected in the arctic fox in Svalbard, Eucoleus aerophilus, Uncinaria stenocephala, Toxocara canis, Trichuris vulpis, Eimeria spp., and Enterocytozoon bieneusi, the latter never found in the arctic fox species before. In addition, only one parasite was found in the sibling vole in Svalbard, the Cryptosporidium alticolis, which has never been detected in Svalbard before.

Background Biologging now allows detailed recording of animal movement, thus informing behavioural ecology in ways unthinkable just a few years ago. In particular, combining GPS and accelerometry allows spatially explicit tracking of various behaviours, including predation events in large terrestrial mammalian predators. Specifically, identification of location clusters resulting from prey handling allows efficient location of killing events. For small predators with short prey handling times, however, identifying predation events through technology remains unresolved. We propose that a promising avenue emerges when specific foraging behaviours generate diagnostic acceleration patterns. One such example is the caching behaviour of the arctic fox (Vulpes lagopus), an active hunting predator strongly relying on food storage when living in proximity to bird colonies. Methods We equipped 16 Arctic foxes from Bylot Island (Nunavut, Canada) with GPS and accelerometers, yielding 23 fox-summers of movement data. Accelerometers recorded tri-axial acceleration at 50 Hz while we obtained a sample of simultaneous video recordings of fox behaviour. Multiple supervised machine learning algorithms were tested to classify accelerometry data into 4 behaviours: motionless, running, walking and digging, the latter being associated with food caching. Finally, we assessed the spatio-temporal concordance of fox digging and greater snow goose (Anser caerulescens antlanticus) nesting, to test the ecological relevance of our behavioural classification in a well-known study system dominated by top-down trophic interactions. Results The random forest model yielded the best behavioural classification, with accuracies for each behaviour over 96%. Overall, arctic foxes spent 49% of the time motionless, 34% running, 9% walking, and 8% digging. The probability of digging increased with goose nest density and this result held during both goose egg incubation and brooding periods. Conclusions Accelerometry combined with GPS allowed us to track across space and time a critical foraging behaviour from a small active hunting predator, informing on spatio-temporal distribution of predation risk in an Arctic vertebrate community. Our study opens new possibilities for assessing the foraging behaviour of terrestrial predators, a key step to disentangle the subtle mechanisms structuring many predator–prey interactions and trophic networks.

Global climate change induces species range shifts and population expansion to higher latitudes in response to rising temperatures. One consequence of climate-induced range shifts is an increased sympatry between related but previously isolated species, potentially resulting in interspecific interactions and hybridization. The Arctic is more rapidly affected by climate warming than any region on Earth and resident species may be prone to interspecific hybridization due to the immigration of new colonizing species. The red fox Vulpes vulpes expanded its range into the Arctic during the twentieth century and is now in sympatry with the native Arctic fox Vulpes lagopus in many places. In this context, an Arctic-like fox displaying an unusual reddish winter coat was observed in 2013 in Nunavut, Canada, a phenotype unknown by Inuit people to date. In this study, we assessed the biological origin of this specimen with a multigenic approach using markers located on mitochondrial DNA, sex (X and Y) chromosomes, and autosomes (microsatellites and the melanocortin 1 receptor (MC1R) gene; a gene involved in the color polymorphism in canids). Our comparative analyses with genetic material from Arctic and red foxes displaying “classic” phenotypes (N = 14 and 16, respectively) suggested a pure Arctic fox origin of the specimen. Specifically, this fox yielded mtDNA, X-linked, Y-linked, and MC1R alleles specific to Arctic fox. Bayesian genetic assignment based on 16 microsatellite loci assigned it to Arctic fox with high confidence (q = 99.7%). Thus, a recent hybrid origin for this specimen is excluded. This alternative winter coat color polymorphism in Arctic fox requires further analyses to determine its underlying genetic mechanism.

Arctic Alaska is an important breeding ground for many migratory bird populations. A variety of factors associated with industrial development may impact nesting birds in this region, including increased nest predator populations associated with anthropogenic nesting and perching sites and the availability of anthropogenic food sources. We tested the indirect impact of oil development on nest survivorship in an artificial nest experiment at Prudhoe Bay, Alaska, 2012–2014, by establishing and monitoring 268 artificial shorebird nests and 221 artificial waterfowl nests and through monitoring of real shorebird nests (n = 186). Distance to infrastructure and roads, and area of infrastructure within 2 km2 of the nest did not significantly affect nest survival of artificial or real nests. Artificial nest survival was higher at shorebird than waterfowl nests. Cameras deployed at a subset of artificial shorebird nests documented nest predation by Arctic fox (Alopex lagopus), red fox (Vulpes vulpes), parasitic jaegers (Stercorarius parasiticus), pomarine jaegers (Stercorarius pomarinus), long-tailed jaegers (Stercorarius longicaudus), northern harriers (Circus cyaneus), and glaucous gulls (Larus hyperboreus). The presence of a camera had a positive effect on artificial shorebird nest survival, possibly due to cameras being placed on progressively older nests throughout the season. In conclusion, we did not detect an effect from infrastructure on nest survival at the scale of the study, in either real or artificial nests. We suggest caution when using artificial nests for Arctic research, given differences in survival of real and artificial nests in this study, and potential differences in nest predators.

In territorial species, observed density dependence is often manifest in lowered reproductive output at high population density where individuals have fewer resources or are forced to inhabit low-quality territories. The Arctic fox (Vulpes lagopus) in Iceland is territorial throughout the year and feeds mostly on birds, since lemmings are absent from the country. Thus, the population does not exhibit short-term population cycles that are evident in most of the species' geographical range. The population has, however, gone through a major long-term fluctuation in population size. Because of the stability in hunting effort and reliable hunting records since 1958, the total number of adult foxes killed annually can be used as an index of population size (N t ). An index of carrying capacity (K) from population growth data for five separate time blocks during 1958-2007 revealed considerable variation in K and allowed a novel definition of population density in terms of K, or N t /K. Correlation analysis suggested that the reproductive rate was largely determined by the proportion of territorial foxes in the population. Variation in litter size and cub mortality was, on the other hand, related to climatic variation. Thus, Arctic foxes in Iceland engage in typical contest competition but can adapt their territory sizes in response to both temporal and spatial variation in carrying capacity, resulting in surprisingly little variation in litter size.

Arctic foxes Vulpes lagopus (L.) display a sharp 3- to 5-year fluctuation in population size where lemmings are their main prey. In areas devoid of lemmings, such as Iceland, they do not experience short-term fluctuations. This study focusses on the population dynamics of the arctic fox in Iceland and how it is shaped by its main prey populations. Hunting statistics from 1958-2003 show that the population size of the arctic fox was at a maximum in the 1950s, declined to a minimum in the 1970s, and increased steadily until 2003. Analysis of the arctic fox population size and their prey populations suggests that fox numbers were limited by rock ptarmigan numbers during the decline period. The recovery of the arctic fox population was traced mostly to an increase in goose populations, and favourable climatic conditions as reflected by the Subpolar Gyre. These results underscore the flexibility of a generalist predator and its responses to shifting food resources and climate changes.

The decline or recolonization of apex predators such as wolves and lynx, often driven by management decisions, and the expansion of smaller generalist predators such as red foxes, can have important ecosystem impacts. The mesopredator release hypothesis proposes that apex predators control medium-sized predator populations through competition and/or intraguild predation. The decline of apex predators thus leads to an increase in mesopredators, possibly with a negative impact on prey populations. Information about the abundance of mammalian tundra predators, wolf (Canis lupus), wolverine (Gulo gulo), lynx (Lynx lynx), red fox (Vulpes vulpes) and arctic fox (Vulpes lagopus) was collected from local active outdoors people during semi-structured interviews in 14 low arctic or sub-arctic settlements in western Eurasia. The perceived abundance of red fox decreased with higher wolf abundance and in more arctic areas, but the negative effect of wolves decreased in more arctic and therefore less productive ecosystems. The perceived abundance of arctic fox increased towards the arctic and in areas with colder winters. Although there was a negative correlation between the two fox species, red fox was not included in the model for perceived arctic fox abundance, which received most support. Our results support the mesopredator release hypothesis regarding the expansion of red foxes in subarctic areas and indicate that top-down control by apex predators is weaker in less productive and more arctic ecosystems. We showed that local ecological knowledge is a valuable source of information about large-scale processes, which are difficult to study through direct biological investigations.

Identifying correctly trophic interactions is important for understanding population dynamics and ecosystem functioning. However, some predator–prey relationships may still remain undetected, due to the difficulty of observing rare predation events. We report the first observation of predation of arctic fox (Vulpes lagopus) pups by common ravens (Corvus corax). The predation event was witnessed on Bylot Island, Nunavut, Canada, through an automatic camera placed on a den. On June 8, 2013, the day following pup emergence from the den, the complete litter of four was killed and taken away by a pair of ravens despite the intermittent presence of the mother. This event lasted 2.5 h, occurred during a low lemming year, and resulted in the fox pair failing their reproduction. Only two other fox litters were present that summer in our 600 km2 study area, so this litter predated by ravens accounted for 25 % (4/16) of the pups produced. Our report shows how continuous monitoring of dens using automatic cameras can allow documentation of rare events. In addition to food competition and cache raiding, pup predation contributes to the antagonistic interactions between arctic foxes and ravens in the High Arctic, which may intensify during low lemming years. This observation allows a better understanding of species interactions within the Arctic predator guild.

After infection with Trichinella spp. was first demonstrated in the arctic fox population in Svalbard 30 years ago, there have been changes in the Svalbard ecosystem related to abundance of polar bear and walrus, both reservoir species for Trichinella. In order to update the assessment of the infection rate and search for differences between sex, age, trapping season and location of trapping sites, we examined arctic foxes from Svalbard in 1996–2004 (n = 429) for antibodies against Trichinella spp. For support and muscle larvae (ML) identification, the diaphragm of a subsample of 330 of the foxes, 40 foxes from 2007 to 2008, and a polar bear (Ursus maritimus) tongue sample, were examined for ML by an HCl–pepsin digestion method. The antibody assay (enzyme-linked immunosorbent assay, ELISA) demonstrated a seroprevalence of 11.7 %. The prevalence increased with age, was similar in females and males, and body condition was similar in seropositives and seronegatives. There were differences in prevalence between trapping seasons and sites. A previously reported spatial (north–south) difference appeared to be eliminated. The seroprevalence was significantly higher in males (50.0 %) than females (20.0 %) of age 4 years and older. An ML prevalence of 6.7 % was demonstrated for the foxes. This was probably an underestimate due to small sample weights. ML were found also in the polar bear. Multiplex PCR identified eleven ML isolates, ten from the arctic foxes and the polar bear isolate, as Trichinella nativa.

With increased polar anthropogenic activity, such as from the oil and gas industry, there are growing concerns about how Arctic species will be affected. Knowledge of species’ sensory abilities, such as auditory sensitivities, can be used to mitigate the effects of such activities. Herein, behavioral audiograms of two captive adult Arctic foxes (Vulpes lagopus) were measured using a yes/no paradigm and descending staircase method of signal presentation. Both foxes displayed a typical mammalian U-shaped audiometric curve, with a functional hearing range of 125 Hz–16 kHz (sensitivity ≤ 60 dB re: 20 μPa) and average peak sensitivity of 24 dB re: 20 μPa at 4 kHz. The foxes had a lower frequency range and sensitivity than would be expected when compared to previous audiograms of domestic dogs (Canis familiaris) and other carnivores. These differences indicate Arctic foxes (V. lagopus) may have a lower frequency range than previously expected, which was similar to the only other fox species tested to date, kit foxes (Vulpes macrotis). Alternatively, differences may be due to testing constraints, such as masking of test signals by ambient noise and/or an unintentionally trained conservative response bias, which most likely resulted in underestimated hearing curves. While results of this study should be interpreted with caution due to its limitations, findings indicate that foxes have a narrower frequency range than formerly presumed. Anthropogenic activities near fox habitats can mitigate their impacts by reducing noise at frequencies within the functional hearing range and peak sensitivities of this species.

In the twentieth century, red fox (Vulpes vulpes) expanded into the Canadian Arctic, where it competes with arctic fox (Vulpes lagopus) for food and shelter. Red fox dominates in physical interactions with the smaller arctic fox, but little is known about competition between them on the tundra. On Hershel Island, north Yukon, where these foxes are sympatric, we focused on natal den choice, a critical aspect of habitat selection. We tested the hypothesis that red fox displaces arctic fox from dens in prey-rich habitats. We applied an approach based on model comparisons to analyse a 10-year data set and identify factors important to den selection. Red fox selected dens in habitats that were more prey-rich in spring. When red foxes reproduced, arctic fox selected dens with good springtime access, notably many burrows unblocked by ice and snow. These provided the best refuge early in the reproductive season. In the absence of red foxes, arctic foxes selected dens offering good shelter (i.e. large isolated dens). Proximity to prey-rich habitats was consistently less important than the physical aspects of dens for arctic fox. Our study shows for the first time that red foxes in the tundra select dens associated primarily with prey-rich areas, while sympatric arctic foxes do not. These results fit a model of red fox competitively interfering with arctic fox, the first detailed study of such competition in a true arctic setting.

Food availability can impact group formation in Carnivora. Specifically, it has been suggested that temporal variation in food availability may allow a breeding pair to tolerate additional adults in their territory at times when food abundance is high. We investigate group occurrence and intraspecific tolerance during breeding in a socially flexible canid, the arctic fox (Vulpes lagopus). We compare Iceland and Sweden where resource conditions differ considerably. A breeding pair was the most common social unit in both populations, but as predicted, groups were more frequent where food abundance varied substantially between years (Sweden: 6 %) than where food availability was stable (Iceland: ≤2 %). Within Sweden, supplemental feeding increased group occurrence from 6 to 21 %, but there was no effect of natural variation in lemming (Lemmus lemmus) availability since group formation was rare also at lemming highs. Thus, additional factors appeared to influence the trade-off between intraspecific territoriality and tolerance. We report two cases where related females showed enduring social relationships with good-neighbour strategies. Related females also engaged in alloparental behaviour in a ‘fox town’ with 31 foxes (4 adults, 3 litters). In contrast, when unrelated foxes bred close to each other, they moved or split their litters during summer, presumably because of territorial conflict. We suggest that fluctuating food availability is linked to group formation in this Arctic carnivore, but also when food availability increases, additional factors such as relatedness, alloparental benefits, competition and predator defence appear necessary to explain group formation.

The reproduction of many species depends strongly on variation in food availability. The main prey of the arctic fox in Fennoscandia are cyclic small rodents, and its number of litters and litter size vary depending on the phase of the rodent cycle. In this experiment, we studied if the arctic fox adjusts its reproduction as a direct response to food abundance, in accordance with the food limitation hypothesis, or if there are additional phase-dependent trade-offs that influence its reproduction. We analysed the weaning success, i.e. proportion of arctic fox pairs established during mating that wean a litter in summer, of 422 pairs of which 361 were supplementary winter fed, as well as the weaned litter size of 203 litters of which 115 were supplementary winter fed. Females without supplementary winter food over-produced cubs in relation to food abundance in the small rodent increase phase, i.e. the litter size was equal to that in the peak phase when food was more abundant. The litter size for unfed females was 6.38 in the increase phase, 7.11 in the peak phase and 3.84 in the decrease phase. The litter size for supplementary winter-fed litters was 7.95 in the increase phase, 10.61 in the peak phase and 7.86 in the decrease phase. Thus, feeding had a positive effect on litter size, but it did not diminish the strong impact of the small rodent phase, supporting phase-dependent trade-offs in addition to food determining arctic fox reproduction.

During the last century, the red fox (Vulpes vulpes) has expanded its distribution into the Arctic, where it competes with the arctic fox (Vulpes lagopus), an ecologically similar tundra predator. The red fox expansion correlates with climate warming, and the ultimate determinant of the outcome of the competition between the two species is hypothesized to be climate. We conducted aerial and ground fox den surveys in the northern Yukon (Herschel Island and the coastal mainland) to investigate the relative abundance of red and arctic foxes over the last four decades. This region has undergone the most intense warming observed in North America, and we hypothesized that this climate change led to increasing dominance of red fox over arctic fox. Results of recent surveys fall within the range of previous ones, indicating little change in the relative abundance of the two species. North Yukon fox dens are mostly occupied by arctic fox, with active red fox dens occurring sympatrically. While vegetation changes have been reported, there is no indication that secondary productivity and food abundance for foxes have increased. Our study shows that in the western Arctic of North America, where climate warming was intense, the competitive balance between red and arctic foxes changed little in 40 years. Our results challenge the hypotheses linking climate to red fox expansion, and we discuss how climate warming’s negative effects on predators may be overriding positive effects of milder temperatures and longer growing seasons.

Many species of colonial ground-nesting birds are known to be sensitive to predation by terrestrial predators. The response of prey under the pressure of predation can either be direct (depletion of prey) or indirect due to prey avoiding the predator. We studied the recolonization of arctic foxes into a large and growing breeding colony of lesser black-backed gulls. The gull colony reached the size of 20,000 pairs during the period of no foxes. The number of breeding gulls continued to increase after the colonization of foxes and reached a maximum of 40,000 pairs about 15 years later. During the same time period, the spatial coverage of the gull colony shrunk from 31.4 down to 18.6 km2, and the change in distribution was closely linked with position of fox dens, which ranged in number from one to three annually. In 2005, the number of breeding gulls decreased slightly with an ongoing shrinkage in spatial coverage. Food analyses from fox scats and stomachs showed that birds of the order Charadriiformes, particularly gulls, were the key prey item. Survival rates of gull nests were higher in the middle of the colony than at the colony edge close to a fox den. The colony area lost could be explained solely by the number of eggs removed by foxes but is unlikely, e.g., due to reclutching. We suggest that intraspecific predation contributes additionally to the effects of direct fox predation although to an unknown degree.

We examined how large seasonal influxes of migratory prey influenced population dynamics of arctic foxes and how this varied with fluctuations in small mammal (lemming and vole) abundance—the main prey of arctic foxes throughout most of their range. Specifically, we compared how arctic fox abundance, breeding density and litter size varied inside and outside a large goose colony and in relation to annual variation in small mammal abundance. Information-theoretic model selection showed that (1) breeding density and fox abundance were 2–3 times higher inside the colony than they were outside the colony and (2) litter size, breeding density and annual variation in fox abundance in the colony tracked fluctuations in lemming abundance. The influence of lemming abundance on reproduction and abundance of arctic foxes outside the colony was inconclusive, largely because fox densities outside the colony were low, which made it difficult to detect such relationships. Lemming abundance was, thus, the main factor governing reproduction and abundance of arctic foxes in the colony, whereas seasonal influxes of geese and their eggs provided foxes with external subsidies that elevated breeding density and fox abundance above that which lemmings could support. This study highlights (1) the relative importance of migratory prey and other foods on the abundance and reproduction by local consumers and (2) how migratory animals function as vectors of nutrient transfer between distant ecosystems such as Arctic environments and wintering areas by geese thousands of kilometres to the south.

Here, we report from the first direct observation of a red fox (Vulpes vulpes) intrusion on an arctic fox (Vulpes lagopus) breeding den from the southern Arctic tundra of Yamal Peninsula, Russia in 2007. At the same time, as a current range retraction of the original inhabitant of the circumpolar tundra zone the arctic fox is going on, the red fox is expanding their range from the south into arctic habitats. Thus, within large parts of the northern tundra areas the two species are sympatric which gives opportunities for direct interactions including interference competition. However, direct first-hand observations of such interactions are rare, especially in the Russian Arctic. In the present study, we observed one red fox taking over an arctic fox breeding den which resulted in den abandonment by the arctic fox. On July 19, eight arctic fox pups were observed on the den before the red fox was observed on the same den July 22. The pups were never seen at the den or elsewhere after the red fox was observed on the den for as long as we stayed in the area (until August 10). Our observation supports the view that direct interference with red fox on breeding dens may contribute to the range retraction of arctic foxes from the southern limits of the Arctic tundra in Russia.

Lemmings are involved in several important functions in the Arctic ecosystem. The Arctic fox (Vulpes lagopus) can be divided into two discrete ecotypes: "lemming foxes" and "coastal foxes". Crashes in lemming abundance can result in pulses of "lemming fox" movement across the Arctic sea ice and immigration into coastal habitats in search for food. These pulses can influence the genetic structure of the receiving population. We have tested the impact of immigration on the genetic structure of the "coastal fox" population in Svalbard by recording microsatellite variation in seven loci for 162 Arctic foxes sampled during the summer and winter over a 5-year period. Genetic heterogeneity and temporal genetic shifts, as inferred by STRUCTURE simulations and deviations from Hardy-Weinberg proportions, respectively, were recorded. Maximum likelihood estimates of movement as well as STRUCTURE simulations suggested that both immigration and genetic mixture are higher in Svalbard than in the neighbouring "lemming fox" populations. The STRUCTURE simulations and AMOVA revealed there are differences in genetic composition of the population between summer and winter seasons, indicating that immigrants are not present in the reproductive portion of the Svalbard population. Based on these results, we conclude that Arctic fox population structure varies with time and is influenced by immigration from neighbouring populations. The lemming cycle is likely an important factor shaping Arctic fox movement across sea ice and the subsequent population genetic structure, but is also likely to influence local adaptation to the coastal habitat and the prevalence of diseases.

The Fennoscandian arctic fox (Vulpes lagopus) population is endangered due to overharvest and competition with the larger red fox (Vulpes vulpes). In this study, we have screened the population in Sweden for endoparasites by analysis of non-invasively faecal samples collected at reproductive dens during two summers, one with low food abundance (2008) and the other with high food abundance (2010). Eggs, larvae and oocysts of a total of 14 different endoparasites were identified with a species richness per inhabited den of 3.2 (CI95% ± 0.48) in 2008 and 2.7 (CI95% ± 0.72) in 2010. Capillariidae-like eggs was identified at 59% of the dens in 2008 and 57% in 2010 and Toxocara canis with 7% (2008) and 30% (2010); Toxascaris leonina with 93% (2008) and 65% (2010); Uncinaria stenocephala 65% (2008) and 39% (2010); Crenosoma vulpis 3% (2008) and 4% (2010); Trichuris sp. 7% (2008) and 4% (2010); Cystoisospora canis-like oocysts 28% (2008) and 26% (2010); Cystoisospora ohiensis-like oocysts 38% (2008) and 4% (2010); Eimeria sp. 7% (2008) and 9% (2010); Sarcocystis sp. 3% (2008) and 9% (2010); Taenia sp. 10% (2008) and 4% (2010); Mesocestoides sp. 3% (2008) and 0% (2010); Balantidium sp. 0% (2008) and 9% (2010) and Spiruroidea-like eggs 0% (2008) and 4% (2010). To our knowledge, Balantidium sp., Sarcocystis sp. and Trichuris sp. has never been described before in wild arctic foxes.

Prion diseases are fatal neurodegenerative disorders of humans and certain other mammals. Prion protein gene (Prnp) is associated with susceptibility and species barrier to prion diseases. No natural and experimental prion diseases have been documented to date in Arctic fox. In the present study, coding region of Prnp from 135 Arctic foxes were cloned and screened for polymorphisms. Our results indicated that the Arctic fox Prnp open reading frame (ORF) contains 771 nucleotides encoding 257 amino acids. Four single nucleotide polymorphisms (SNPs) (G312C, A337G, C541T, and A723G) were identified. SNPs G312C and A723G produced silent mutations, but SNPs A337G and C541T resulted in a M-V change at codon 113 and R-C at codon 181, respectively. The Arctic fox Prnp amino acid sequence was similar to that of the dog (XM 542906). In short, this study provides preliminary information about genotypes of Prnp in Arctic fox.

The extensive use of sea-ice by three arctic foxes (Alopex lagopus) in northern Alaska was documented using satellite telemetry during the winter of 2005-2006. Here we present the Wrst detailed data on movements of individual foxes while on the sea-ice. Two juvenile males and one juvenile female traveled long distances (904, 1,096, and 2,757 km) and remained on the sea-ice for extended periods of time (76, 120, and 156 days). Average distances traveled per day ranged from 7.5 to 17.6 km and foxes achieved maximum rates of travel of up to 61 km/ day. These Wndings verify the use of sea-ice by arctic foxes and raise concerns that the diminishing arctic ice cover may negatively impact populations by limiting access to marine food sources.

After a marked decline at the beginning of the 1900s, the arctic fox Alopex lagopus population in Fennoscandia has remained at a very low level. We suggest that the main cause for the population crash was winter starvation caused by (1) over-hunting of reindeer Rangifer tarandus populations, and thus reduced carcass availability in the mountains, and (2) increased interspecific competition for these carcasses because of increased invasion of red foxes Vulpes vulpes from lower altitudes. The failure of arctic fox populations to recover, despite increasing reindeer populations in the mid 1900s, can be explained by a concurrent strong increase in red fox numbers. Analyses of countywide hunting statistics from Norway 1891–1920 suggest that there actually was an increase in red fox numbers in the period of arctic fox decline, and that the increase in reindeer populations from the 1920s to the 1950s was accompanied by a new increase in red fox numbers. We conclude that restoring arctic fox populations most likely will require a substantial and lasting reduction of red fox populations.

Cache recovery is critical for evolution of hoarding behaviour, because the energy invested in caching may be lost if consumers other than the hoarders benefit from the cached food. By raiding food caches, animals may exploit the caching habits of others, that should respond by actively defending their caches. The arctic fox (Alopex lagopus) is the main predator of lemmings and goose eggs in the Canadian High Arctic and stores much of its prey in the ground. Common ravens (Corvus corax) are not as successful as foxes in taking eggs from goose nests. This generalist avian predator regularly uses innovation and opportunism to survive in many environments. Here, we provide the first report that ravens can successfully raid food cached by foxes, and that foxes may defend their caches from ravens.

In Scandinavia, farmed arctic foxes frequently escape from farms, raising concern about hybridization with the endangered wild population. This study was performed to find a genetic marker to distinguish escaped farm foxes from wild Scandinavian foxes. Microsatellite and mitochondrial control region variation were analyzed in 41 farm foxes. The results were compared with mitochondrial and microsatellite data from the wild population in Scandinavia. The farm foxes were genetically distinct from the wild foxes (FST=0.254, P < 0.00001) and all farm foxes had a single control region haplotype different from those observed in the wild population. We developed a method based on Restriction Fragment Length Polymorphism (RFLP) on the mitochondrial control region to differentiate between farmed and wild arctic foxes. This test was subsequently successfully used on 25 samples from free-ranging foxes, of which four had a suspected farm origin. All four of the suspected foxes, and none of the others, carried the farm fox haplotype. Three of these were successfully genotyped for all eleven microsatellite loci. A population assignment test and a Bayesian Markov Chain Monte Carlo analysis indicated that two of these individuals were escaped farm foxes, and that the third possibly was a hybrid between a farmed and a wild arctic fox.

Metabolic rates of four resting, post-absorptive male adult summer- and winter-adapted captive arctic foxes (Alopex lagopus) were recorded. Basal metabolic rates (BMR) varied seasonally with a 36% increase from winter to summer, while body mass was reduced by 17% in the same period. The lower critical temperature (T 1c) of the winter-adapted arctic fox was estimated to −7°C, whereas T lc during summer was 5°C. The similarity of these values, which are much higher than hitherto assumed (e.g. Scholander et al. 1950b), is mainly due to a significantly (P

The spatial distribution of 33 Arctic fox dens on Bering Island was studied, and a relationship between the burrowing activity of Arctic foxes and the pattern of vegetation near their dens was revealed. This activity was shown to change the structure of the plant cover, with the degree of change depending on the type of biotope.

Age-related changes of content of thyroid hormones in the blood serum and of activities of lysosomal proteinases in organs were studied in the arctic fox Alopex lagopus L. in early postnatal ontogenesis. The existence has been shown of a negative correlation between the age changes in the serum thyroxin content and lysosomal proteinase activities in some organs of these animals. The results obtained indicate predominance of anabolic function of thyroid hormones in arctic fox cubs. The problem of anabolic and catabolic effects of thyroid hormones on protein metabolism is discussed.

Arctic fox (Alopex lagopus) numbers vary greatly, with cyclic fluctuations often associated with fluctuations in microtine rodents. However, in areas where small prey mammals are absent, such as Iceland and Svalbard, such cyclic fluctuations are lacking. Annual fluctuations in the density of the arctic fox population on the Broggerhalvoya peninsula and Kongsfjorden region on Svalbard, Norway, were studied from 1990 to 2001 by using indices of fox abundance. All indices showed similar trends; fox numbers were low in 1990, increased until 1995 whereupon they decreased sharply, before increasing again and levelling off in 2001. Increasing numbers of foxes during the first part of the study paralleled increasing numbers of Svalbard reindeer (Rangifer tarandus platyrhynchus) carcasses in winter and increasing numbers of nesting barnacle geese (Branta leucopsis) in summer. This study shows that the number of arctic foxes varies greatly even in areas without fluctuating microtine rodents.

Consumption of marine foods by terrestrial predators can lead to increased predator densities, potentially impacting their terrestrial resources. For arctic foxes (Alopex lagopus), access to such marine foods in winter depends on sea ice, which is threatened by global climate change. To quantify the importance of marine foods (seal carrion and seal pups) and document temporal variation in arctic fox diet I measured the ratios of the stable isotopes of carbon ((13)C/(12)C) in hair of arctic foxes near Cape Churchill, Manitoba, from 1994 to 1997. These hair samples were compared to the stable carbon isotope ratios of several prey species. Isotopic differences between seasonally dimorphic pelage types indicated a diet with a greater marine content in winter when sea ice provided access to seal carrion. Annual variation in arctic fox diet in both summer and winter was correlated with lemming abundance. Marine food sources became much more important in winters with low lemming populations, accounting for nearly half of the winter protein intake following a lemming decline. Potential alternative summer foods with isotopic signatures differing from lemmings included goose eggs and caribou, but these were unavailable in winter. Reliance on marine food sources in winter during periods of low lemming density demonstrates the importance of the sea ice as a potential habitat for this arctic fox population and suggests that a continued decline in sea ice extent will disrupt an important link between the marine and terrestrial ecosystems.

The distribution of many predators may be limited by interactions with larger predator species. The arctic fox in mainland Europe is endangered, while the red fox is increasing its range in the north. It has been suggested that the southern distribution limit of the arctic fox is determined by interspecific competition with the red fox. This has been criticised, on the basis that the species co-exist on a regional scale. However, if the larger red fox is superior and interspecific competition important, the arctic fox should avoid close contact, especially during the breeding season. Consequently, the distribution of breeding dens for the two species would be segregated on a much smaller spatial and temporal scale, in areas where they are sympatric. We tested this hypothesis by analysing den use of reproducing arctic and red foxes over 9 years in Sweden. High quality dens were inhabited by reproducing arctic foxes more often when no red foxes bred in the vicinity. Furthermore, in two out of three cases when arctic foxes did reproduce near red foxes, juveniles were killed by red foxes. We also found that breeding arctic foxes occupied dens at higher altitudes than red foxes did. In a large-scale field experiment, red foxes were removed, but the results were not conclusive. However, we conclude that on the scale of individual territories, arctic foxes avoid areas with red foxes. Through interspecific interference competition, the red fox might thus be excluding the arctic fox from breeding in low altitude habitat, which is most important in years when food abundance is limited and competition is most fierce. With high altitude refuges being less suitable, even small-scale behavioural effects could scale up to significant effects at the population level.

Isozymes of lactate dehydrogenase extracted from heart, kidney, and liver of mink (Mustela vison Briss.) and Arctic fox (Alopex lagopus L.) during postnatal development were separated by agarose gel electrophoresis. Tissue-specific isozyme pattern of lactate dehydrogenase can be revealed at the age of one month, while the definitive pattern is formed at the age of four months. The isozyme patterns of lactate dehydrogenase in the studied tissues of mink and Arctic fox share the properties specific for animal species of various ecogenesis.

High terrains might have been training ground for cold adaptation before the Ice Age struck.

A complete set of paint probes, with each probe specific for a single type of dog chromosome, was generated by DOP-PCR amplification of flow-sorted chromosomes. These probes have been assigned to high-resolution G-banded chromosomes of the dog and Arctic fox by fluorescence in-situ hybridization. On the basis of these results we propose improved nomenclature for the G-banded karyotypes of the dog and Artic fox. A comparative map between the Arctic fox, red fox and dog has been established based on results from chromosome painting and high-resolution G-banding. This map demonstrates that the euchromatic complements of these three canid species consists of 42 conserved segments. Thirty-four of these 42 segments are each represented by a single dog chromosome with dog chromosomes 1, 13, 18 and 19 each retaining two segments, respectively. The autosomes of the Arctic fox and red fox could be reconstructed from these 42 blocks in different combinations through chromosomal fusions. Our findings suggest that chromosome fusion has been the principal mechanism of karyotype evolution occuring during speciation in canids.

The Canadian Arctic is characterized by a high variation in landform types and there are complex interactions between land, water and the atmosphere which dramatically affect the distribution of biota. Biodiversity depends upon the intensity, predictability and scale of these interactions. Observations, as well as predictions of large-scale climate models which include ocean circulation, reveal an anomalous cooling of northeastern Canada in recent decades, in contrast to the overall significant increase in average annual temperature in the Northern Hemisphere. Predictions from models are necessary to forecast the change in the treeline in the 21st century which may lead to a major loss of tundra. The rate of change in vegetation in response to climate change is poorly understood. The treeline in central Canada, for example, is showing infilling with trees, and in some locations, northerly movement of the boundary. The presence of sea ice in Hudson Bay and other coastal areas is a major factor affecting interactions between the marine and terrestrial ecosystems. Loss of ice and therefore hunting of seals by polar bears will reduce bear and arctic fox populations within the region. In turn, this is likely to have significant effects on their herbivorous prey populations and forage plants. Further, the undersurface of sea ice is a major site for the growth of algae and marine invertebrates which in turn act as food for the marine food web. A rise in sea-level may flood coastal saltmarsh communities leading to changes in plant assemblages and a decline in foraging by geese and other consumers. The anomalous cooling in the eastern Arctic, primarily in late winter and early spring, has interrupted northern migration of breeding populations of geese and ducks and led to increased damage to vegetation in southern arctic saltmarshes as a result of foraging. It is likely that there has been a significant loss of invertebrates in those areas where the vegetation has been destroyed. Warming will have major effects on permafrost distribution and on ground-ice resulting in a major destabilization of slopes and slumping of soil, and disruption of tundra plant communities. Disruption of peat and moss surfaces lead to loss of insulation, an increase in active-layer depth and changes in drainage and plant assemblages. Increases of UV-B radiation will strongly affect vulnerable populations of both plants and animals. The indigenous peoples will face major changes in life style, edibility of food and health standards, if there is a significant warming trend. The great need is for information which is sensitive to the changes and will assist in developing an understanding of the complex interactions of the arctic biota, human populations and the physical environment.

Summary The coccidian protozoan Toxoplasma gondii has a world-wide distribution. It causes toxoplasmosis, a potentially very serious disease to humans and other warm-blooded animals. Infection has in many studies been shown to be rather common in the Nordic countries also, where its prevalence both in domestic animals and wildlife can be explained by contacts with cats and their faeces, cats and wild felids being the only definitive hosts of the parasite known. Before the discovery of the complete life cycle of the parasite, other infection routes to animals were studied e.g. in Russia, where lateral transmission of infection in a reindeer herd was reported. The vehicle of infection was apparently body fluids, such as e.g. saliva and lacrimal fluid containing parasite tachyzoites, which might invade another reindeer via mucosal membranes. According to the finding, toxoplasmosis might be apprehended to be also a sexually transmitted disease. Following the discovery of the pivotal role of the cat in the epidemiology of T. gondii, possible alternative pathways of infection have generally been ignored. In Fennoscandian semi-domesticated reindeer, a clear association of the seroprevalence of antibodies to T. gondii was seen with the degree of domestication, and, thus, with cat contacts [1]. In the high Arctic of Svalbard, there is a considerably high seroprevalence of infection both in polar bears and Arctic foxes [2-4]. The source of infection is unlikely to be found in the seals constituting the major part of the polar bear’s diet, as in one study, antibodies were not found in North Atlantic marine mammals. However, in other, less arctic and remote, cetacean and pinniped populations studied, T. gondii infection has been found. Because Svalbard reindeer and sibling voles studied have been free from T. gondii infection, it can be assumed that sexual stages of infection (in definitive hosts) leading to oocyst production is not a major part of the Svalbard T. gondii life cycle [2]. Then, carnivores probably get the infection with food, anyhow. Cannibalism is considered common in polar bears and Arctic foxes, and probably can explain a lot. One parasite isolate from an Arctic fox proved to belong to the Type II strain, the predominant T. gondii lineage in the world [3]. This somewhat objects to the suggested idea of a specific Arctic life cycle of the parasite, but incorporates the Arctic to the globalT. gondii infection network. Further support to the hypothesis is gained from the finding that Svalbard barnacle geese (Branta leucopsis) are rather commonly infected. They may get the infection when wintering in Scotland. So, perhaps migratory birds are important in T. gondii globalisation. Cats are crucial to T. gondii epidemiology. However, the Arctic example proves that the successful parasite can thrive even in the absence of cats.

The bladderworm Pearsonema (syn Capillaria) plica affects domestic dogs and wild carnivores worldwide. A high prevalence in red foxes (Vulpes vulpes) has been reported in many European countries. P. plica inhabits the lower urinary tract and is considered to be of low pathogenic significance in dogs mostly causing asymptomatic infections. However, a higher level of pathogenicity has been reported in foxes. A severe cystitis associated with numerous bladderworms was found in a captive arctic fox (Vulpes lagopus) originating from the endangered Fennoscandian arctic fox population. To our knowledge this is the first description of P. plica infection in an arctic fox.

We have studied the transcription of highly repeated satellite-like Bsp elements containing the potential promoter boxes for RNA polymerase III in the genomes of adult silver and arctic foxes. The Bsp repeat transcripts were abundant enough to be detected by Northern blot and semiquantitative dot blot hybridizations, and the majority were found in the nuclear RNA fraction from arctic fox kidneys. Weak hybridization signals were revealed with the cytoplasmic RNA preparation from silver fox kidneys and with the nuclear RNA fraction from arctic fox liver, and their intensity was intermediate with the total RNA from arctic fox brain. Taken together, the data suggest possible genomic interspersion of some Bsp repeats in these two representatives of Canidae. The observed species-and tissue-specificity of the transcription of Bsp repeats suggests that they may potentially accomplish regulatory functions in the fox genomes.

A case of human rabies in the arctic zone of Siberia is described. The victim was bitten by a wolf, but characterization of the isolate by monoclonal antibodies showed that it was an arctic fox virus strain. This discovery reaffirmed the value of strain typing rabies virus isolates in regions where this has not been done already: such characterization pertains to the identification of the reservoir host, to the natural history of the virus in the reservoir, and to future surveillance, post-exposure treatment, and public education in the region.

Four arctic fox Alopex lagopus pups (two males and two females) were caught at dens when about 25–53 days old and kept in outdoor pens at NyAlesund, Svalbard. Their growth in body size (as measured by the length of a front foot), increase in weight, and food consumption were monitored from July to December, 1987. The pups grew rapidly and reached 97.5 ± 0.1% of their maximum adult size when they were 99–127 days old. Increase in body weight took longer (130 days). Food consumption generally increased until about 90 days old, after which it was highly variable. Pups consumed on average 266 kcal kg−1 day−1 growing 34g/day until 95 days old. Subsequently, until about 200 days old, they consumed 202 kcal kg−1 day−1 and grew 6.8 g/day.

Concentrations of cadmium, mercury, lead, arsenic, selenium, copper, zinc, manganese and iron in liver, and cadmium in kidneys, were analysed in 95 carcasses of arctic fox (Alopex lagopus) caught in Svalbard during three winter seasons from 1984 through 1986. The hepatic concentration ranges of cadmium, mercury, lead and arsenic were 0.1–2.4, 0.01–2.2, < 0.5–2.9 and 0.01–1.3 μg·g−1 WW, respectively. The range of cadmium concentration in the kidneys was from 0.2 to 13 μg·g−1 WW. Cadmium and mercury concentrations were higher in adult animals than in juveniles. The average concentrations of cadmium and lead were similar to recently published levels in polar bear from Svalbard, but the mercury concentrations were lower. Significant geographical differences were observed between trapping areas. Foxes caught north of Isfjorden had lower levels of liver iron and higher levels of all other elements analysed than those caught south of Isfjorden. The recorded concentrations of heavy metals indicate a moderate degree of exposure, which most likely is of natural origin.

We examined the liver of adult polar bears, arctic foxes, and rats by gold chloride staining, fluorescence microscopy for the detection of autofluorescence of vitamin A, hematoxylin-eosin staining, staining with Masson's trichrome, Ishii and Ishii's silver impregnation, and transmission electron microscopical morphometry. The liver lobules of the arctic animals showed a zonal gradient in the storage of vitamin A. The density (i.e., cell number per area) of hepatic stellate cells was essentially the same among the zones. These results indicate that the hepatic stellate cells of the polar bears and arctic foxes possess heterogeneity of vitamin A-storing capacity in their liver lobules.

Under physiological conditions, hepatic stellate cells store 80 % of the total vitamin A in the whole body as retinyl palmitate in lipid droplets in the cytoplasm, and regulate both transport and storage of vitamin A [1-3]. It has been demonstrated that animal or human individuals exposed to drugs such as methadone, prednisone and phenobarbital, antiepileptics [4], and xenobiotics like the environmental contaminants DDT, PCD and dioxins have dramatic changes in their retinoid metabolism and function. Recent data demonstrate that top predators among Svalbard mammals and birds like polar bear, arctic fox and glaucous gull accumulate relatively large amounts of persistent organic pollutants [5]. Since it has been reported that vitamin A accumulates at near toxic doses in some arctic predators [6] and recent data suggest that PCB and DDT may reduce the threshold for vitamin A-toxicity [7], an increasing accumulation of persistent organic pollutants might eventually precipitate vitamin A-toxicity in these animals. To elucidate the possibility of vitamin A-related toxicity in arctic predators, we have performed a systematic characterization of the hepatic vitamin A-storage, which is the best index of the vitamin A-status, in mammals of the Svalbard archipelago.

Pelage is seasonally dimorphic in the Arctic fox. During the winter, fur lengths for this species are nearly double similar values taken during the summer season. Considerable site-specific differences in fur length are noted. In general, body sites which are exposed to the environment when an Arctic fox lies in a curled position show greater fur lengths in all seasons and greater seasonal variations than body sites that are more protected during rest. Well-furred sites may tend to conserve heat during periods of inactivity, and scantily furred sites may tend to dissipate heat during periods of exercise. The growth of winter fur may compensate for the severe cold of the arctic winter. Changes in fur lengths indicate a definite pattern in spite of individual variations. During the fall months, fur lengths seem to lag behind an increasing body-to-ambient temperature gradient. Both body-to-ambient temperature gradients and fur lengths peak during December through February. From March through June, gradual environmental warming is accompanied by a decrease in average fur lengths. Thus, there appears to be a remarkable parallel between the body-to-ambient temperature gradient and the fur lengths. The growth of fur in the Arctic fox parallels annual changes in ambient temperature and photoperiod.

Starting about 1836 and continuing into the 1930's fur traders and fox farmers introduced arctic fox (Alopex lagopus) to several islands in the Aleutian Chain--islands that were previously free of terrestrial mammalian predators (Jones and Byrd 1979). By 1937, this exotic furbearer was successfully introduced on almost all of the Aleutian Islands. Their effect on native avifauna was immediate and acute since they depended on natural foods, including indigenous birds for sustenance and it soon became a pest of significant importance in the Aleutian Islands. Aleutian Canada geese (Branta canadensis leucopareia) were a major prey species, and by 1967 were listed as endangered. Recovery plans for the Aleutian Canada goose specified the sequential eradication of arctic fox throughout the Aleutian Islands including Kiska Island, a large land mass (28,200 ha) and historic breeding site of this species in the western Aleutians. The investigations of the efficacy of the pesticide sodium fluoroacetate (1080) against arctic fox and the potential hazards

WHITE coloration of many animals in cold environments decreases the possibility of visual detection because of the lack of contrast between the animal and its white background. White hair thus provides concealing coloration for prey species such as arctic hare (Lepus arcticus), and for predators such as the polar bear (Ursus maritimus) and arctic fox (Alopex lagopus).