Lemmus Trimucronatus Research Articles

Influence of habitat on fine-scale space use by brown lemmings (Lemmus trimucronatus) in the High Arctic.

Space use by small mammals should mirror their immediate needs for food and predator shelters but can also be influenced by seasonal changes in biotic and abiotic factors. Lemmings are keystone species of the tundra food web, but information on their spatial distribution in relation to habitat heterogeneity is still scant, especially at a fine scale. In this study, we used spatially explicit capture-recapture methods to determine how topography, hydrology, vegetation, and soil characteristics influence the fine-scale spatial variations in summer density of brown lemmings (Lemmus trimucronatus). Lemmings were monitored throughout the summer in wet and mesic tundra habitats and in a predator exclusion grid, which was also located in mesic tundra. We found that in wet tundra, lemming densities were higher at sites with a rugged topography dominated by hummocks, but only during snow melt. In both mesic tundra sites, lemming densities were higher in sites with poor drainage and low aspect throughout the summer. We found no clear association between lemming densities and any tested vegetation or soil variables. Overall, hydrology and topography appear to play a dominant role in small-scale space use of brown lemmings with a secondary role for predator avoidance and food plant abundance.

Response of vegetation and carbon fluxes to brown lemming herbivory in northern Alaska

Abstract. The warming of the Arctic is affecting the carbon cycle of tundra ecosystems. Most research on carbon fluxes from Arctic tundra ecosystems has focused on abiotic environmental controls (e.g., temperature, rainfall, or radiation). However, Arctic tundra vegetation, and therefore the carbon balance of these ecosystems, can be substantially impacted by herbivory. In this study we tested how vegetation consumption by brown lemmings (Lemmus trimucronatus) can impact carbon exchange of a wet-sedge tundra ecosystem near Utqiaġvik, Alaska during the summer and the recovery of vegetation during the following summer. We placed brown lemmings in individual enclosure plots and tested the impact of lemmings' herbivory on carbon dioxide (CO2) fluxes, methane (CH4) fluxes, and the normalized difference vegetation index (NDVI) immediately after lemming removal and during the following growing season. During the first summer of the experiment, lemmings' herbivory reduced plant biomass (as shown by the decrease in the NDVI) and decreased net CO2 uptake while not significantly impacting CH4 emissions. CH4 emissions were likely not significantly affected due to CH4 being produced deeper in the soil and escaping from the stem bases of the vascular plants. The summer following the lemming treatments, NDVI and net CO2 fluxes returned to magnitudes similar to those observed before the start of the experiment, suggesting a complete recovery of the vegetation and a transitory nature of the impact of lemming herbivory. Overall, lemming herbivory has short-term but substantial effects on carbon sequestration by vegetation and might contribute to the considerable interannual variability in CO2 fluxes from tundra ecosystems.

Snow hardness impacts intranivean locomotion of arctic small mammals

AbstractFossorial locomotion is often considered as the most energetically costly of all terrestrial locomotion. Small arctic rodents, such as lemmings, dig tunnels not only in the soil but also through the snowpack, which is present for over 8 months of the year. Lemmings typically dig in the softest snow layer called the depth hoar but with climate change, melt‐freeze and rain‐on‐snow (ROS) events are expected to increase in the Arctic, leading to a higher frequency of hardened snowpacks. We assessed the impacts of snow hardness on the locomotion of two lemming species showing different morphological adaptations for digging. We hypothesized that an increase in snow hardness would (1) decrease lemming performance and (2) increase their effort while digging, but those responses would differ between lemming species. We exposed four brown lemmings (Lemmus trimucronatus) and three collared lemmings (Dicrostonyx groenlandicus) to snow of different hardness (soft, hard, and ROS) during 30‐min trials (n = 63 trials) in a cold room and filmed their behavior. We found that the digging speed and tunnel length of both species decreased with snow hardness and density, underlining the critical role of snow properties in affecting lemming digging performance. During the ROS trials, time spent digging by lemmings increased considerably and they also started using their incisors to help break the hard snow, validating our second hypothesis. Overall, digging performance was higher in collared lemmings, the species showing more morphological adaptations to digging, than in brown lemmings. We conclude that the digging performance of lemming is highly dependent on snowpack hardness and that the anticipated increase in ROS events may pose a critical energetic challenge for arctic rodent populations.

Direct and indirect effects of regional and local climatic factors on trophic interactions in the Arctic tundra

Climate change can impact ecosystems by reshaping the dynamics of resource exploitation for predators and their prey. Alterations of these pathways could be especially intense in ecosystems characterized by a simple trophic structure and rapid warming trends, such as in the Arctic. However, quantifying the multiple direct and indirect pathways through which climate change is likely to alter trophic interactions and their relative strength remains a challenge. Here, we aim to identify direct and indirect causal mechanisms driven by climate affecting predator-prey interactions of species sharing a tundra food web. We based our study on relationships between one Arctic predator (Arctic fox) and its two main prey - lemmings (preferred prey) and snow geese (alternate prey) - which are exposed to variable local and regional climatic factors across years. We used a combination of models mapping multiple causal links among key variables derived from a long-term dataset (21years). We obtained several possible scenarios linking regional climate factors (Arctic oscillations) and local temperature and precipitation to the breeding of species. Our results suggest that both regional and local climate factors have direct and indirect impacts on the breeding of foxes and geese. Local climate showed a positive causal link with goose nesting success, while both regional and local climate displayed contrasted effects on the proportion of fox breeding. We found no impact of climate on lemming abundance. We observed positive relationships between lemming, fox and goose reproduction highlighting numerical and functional responses of fox to the variability of lemming abundance. Our study measures causal links and strength of interactions in a food web, quantifying both numerical response of a predator and apparent interactions between its two main prey. These results improve our understanding of the complex effects of climate on predator-prey interactions and our capacity to anticipate food web response to ongoing climate change.

Differences in behavior help to explain lemming coexistence

Abstract Collared (Dicrostonyx groenlandicus) and brown (Lemmus trimucronatus) lemmings coexist in tundra habitats across much of the middle and lower Canadian arctic. Their coexistence, and response to predation risk, appears mediated by behavior. We analyzed field-collected videos of open-field tests to assess potential differences in innate behaviors between the two species. Collared lemmings were less active and exhibited less exploratory behavior than did brown lemmings, which were more active under cover than in the open. Similar behaviors scaling along axes of activity and curiosity were revealed by principal components analysis. Each axis defined different aspects of brown lemming personality, but repeated testing of the same individuals yielded a striking dependence of their behavioral response on open-field treatments. Even so, the differences between species in behavior correlate well with their habitat preferences that resolve competition and govern their coexistence.

Demography and Condition of Brown Lemmings (Lemmus trimucronatus) During Cyclic Density Fluctuations Near Barrow, Alaska

We analyzed data collected from 19 428 necropsied brown lemmings (Lemmus trimucronatus) collected over a period of 22 years near Barrow, Alaska. Here we report on seasonal and cyclic patterns in reproductive activity of females and males, population structure, adult body size, condition (weight per unit length and body fat), and wounding. We also provide the first detailed information on these characteristics at low population densities. The seasonal pattern of reproduction included short summers (about 2.5 months) with intense reproduction, long winters (about 6.5 months) with moderate reproduction, and virtual cessation of breeding during the short springs and autumns (1.5 months each). Overall sex ratios appeared equal, but the proportion of males decreased during summer. The proportion of immature lemmings increased in late summer and autumn after intense summer breeding, then declined in winter. Adult body weight and condition (weight per unit length) peaked in summer when the food supply also peaked, but body fat, though still minimal, peaked in winter. The greatest incidence of wounding occurred in males, but wounding increased in both sexes during early summer, the period of most intense breeding. As reported previously for arvicoline rodents, a longer summer reproductive season occurred during the low and increase phases, but no change in litter size occurred during the cycle. Contrary to earlier reports, a much lower frequency of pregnancy occurred during the high phase, but later reproductive maturation during the high phase received little support. The sex ratio generally changed little during the course of a population cycle, but the proportion of females did decline during springs when the population increased to high densities. We found a greater proportion of adults during the high and decreasing phases, reflecting the reduced reproduction during those phases. Higher body weights and better condition of adults occurred during high densities. Wounding (fresh scars from bites) also peaked during years with high densities, though only for adult males and non-reproductive females. Overall, it appeared that nutrition strongly influenced seasonal changes in reproduction, population structure, and body condition; predation affected both seasonal and cyclic changes in population structure and survival; and that nutrition, and perhaps social strife, caused cyclic changes in reproduction, survival, and body size.

Life in the fast lane: learning from the rare multi-year recaptures of brown lemmings in the High Arctic

Inter-annual recaptures of Arctic lemmings are extremely rare because their life expectancy is very short, typically less than one year. On Bylot Island, Nunavut, Canada, we live-trapped in summer, marked and released brown lemmings (Lemmus trimucronatus, Kerr 1792) between 2004 and 2016 and we performed a large-scale, before-after control-impact experiment from 2014 to 2016 to study the effects of predator reduction on their population dynamics. Although inter-annual recaptures of marked lemmings were rare, our long-term study and predator reduction allowed us to capture 21 (1.4%; n = 1523) individuals over two consecutive years and one over three consecutive years. The inter-annual recapture rate was much higher in the predator-reduction grid (5.7%; n = 193) than in the other grids (0.7%; n = 425) during the experiment. Average distance moved between inter-annual recaptures was small (74 m). Our data thus demonstrate that lemmings are physiologically capable of living up to 24 months in the High Arctic, that predation is a major factor affecting lemming survival, including over winter, and that they show high site fidelity among years.

Feeding preference of brown lemmings (Lemmus trimucronatus) for plant parts of Arctic willow (Salix arctica)

Food availability has been proposed to be a factor driving population fluctuations of lemmings in the Arctic. In contrast with previous studies, a recent analysis of faecal pellets and stomach contents of brown lemmings (Lemmus trimucronatus) reported a surprisingly high proportion (34–56%) of willows (Salix spp.) in their diet during both summer and winter in the Canadian high Arctic. To better understand the contribution of willows to the diet of lemmings, we designed a cafeteria experiment to determine which part of Arctic willows (S. arctica), usually the most abundant willow in the Canadian Arctic, were preferred by lemmings. We designed two types of experiments, one with flowering willows (summer stage; n = 10) and one with dormant willows without flowers or leaves (winter stage; n = 11). Lemmings preferred buds and to a lesser extent roots over woody stems in dormant willows, whereas in flowering willows, they preferred flowers and roots over leaves and buds. Our results suggest that lemmings shift their diet seasonally and prefer the fleshiest willow parts, i.e. flowers in summer and buds in winter. High consumption of roots by lemmings in both types of experiments indicates strong underground feeding habits. This behaviour could be favoured by geomorphological processes such as soil upheaves and permafrost thawing that often expose roots to grazing.

Assessing Stress in Arctic Lemmings: Fecal Metabolite Levels Reflect Plasma Free Corticosterone Levels.

Interest in the ecology of stress in wild populations has triggered the development of noninvasive methods for quantifying stress hormones. Measurement of fecal corticosteroid metabolites (FCMs) is one such method, but it is still unclear whether FCMs can be a reliable proxy of free plasma glucocorticoids. To assess the validity of this assumption, we carried out a robust assessment on brown lemmings (Lemmus trimucronatus) from Bylot Island, Nunavut, Canada, that were hand captured and anesthetized and related plasma glucocorticoid levels to fecal metabolite glucocorticoid levels. We examined endogenous factors that could explain interindividual variability. Blood corticosterone was measured from samples obtained on capture and 30 min later, and FCM levels were measured from animals kept in captivity for 72 h. Plasma free corticosterone increased 135-fold over baseline values 30 min after capture, which confirmed that initial handling was perceived as a stressor. We found that FCM levels were highly related with free (marginal [Formula: see text] = 0.53) but not with total ([Formula: see text] = 0.02) corticosterone levels, regardless of age, sex, and reproductive condition. FCM levels started increasing 2 h after capture and reached maximum levels 4 h after capture. No circadian rhythm in FCMs was found. Plasma total corticosterone levels were much higher in adult females compared with adult males, but this difference was much smaller when measuring free corticosterone levels and FCM levels. Our results suggest that FCM levels are good measures of stress by being closely related to plasma free corticosterone levels in brown lemmings.

Top-down limitation of lemmings revealed by experimental reduction of predators.

It is generally recognized that delayed density-dependence is responsible for cyclic population dynamics. However, it is still uncertain whether a single factor can explain why some rodent populations fluctuate according to a 3-4yr periodicity. There is increasing evidence that predation may play a role in lemming population cycles, although this effect may vary seasonally. To address this issue, we conducted an experiment where we built a large exclosure (9ha) to protect brown lemmings (Lemmus trimucronatus) from avian and terrestrial predators. We tested the hypothesis that predation is a limiting factor for lemmings by measuring the demographic consequences of a predator reduction during the growth and peak phases of the cycle. We assessed summer (capture-mark-recapture methods) and winter (winter nest sampling) lemming demography on two grids located on Bylot Island, Nunavut, Canada from 2008 to 2015. The predator exclosure became fully effective in July 2013, allowing us to compare demography between the control and experimental grids before and during the treatment. Lemming abundance, survival and proportion of juveniles were similar between the two grids before the treatment. During the predator-reduction period, summer densities were on average 1.9× higher inside the experimental grid than the control and this effect was greatest for adult females and juveniles (densities 2.4× and 3.4× higher, respectively). Summer survival was 1.6×higher on the experimental grid than the control whereas body mass and proportion of juveniles were also slightly higher. Winter nest densities remained high inside the predator reduction grid following high summer abundance, but declined on the control grid. These results confirm that predation limits lemming population growth during the summer due to its negative impact on survival. However, it is possible that in winter, predation may interact with other factors affecting reproduction and ultimately population cycles.

Molecular systematics and Holarctic phylogeography of cestodes of the genus Anoplocephaloides Baer, 1923 s. s. (Cyclophyllidea, Anoplocephalidae) in lemmings (Lemmus,Synaptomys)

The present molecular systematic and phylogeographic analysis is based on sequences of cytochrome c oxidase subunit 1 (cox1) (mtDNA) and 28S ribosomal DNA and includes 59 isolates of cestodes of the genus Anoplocephaloides Baer, 1923 s. s. (Cyclophyllidea, Anoplocephalidae) from arvicoline rodents (lemmings and voles) in the Holarctic region. The emphasis is on Anoplocephaloides lemmi (Rausch 1952) parasitizing Lemmus trimucronatus and Lemmus sibiricus in the northern parts of North America and Arctic coast of Siberia, and Anoplocephaloides kontrimavichusi (Rausch 1976) parasitizing Synaptomys borealis in Alaska and British Columbia. The cox1 data, 28S data and their concatenated data all suggest that A. lemmi and A. kontrimavichusi are both non‐monophyletic, each consisting of two separate, well‐defined clades, that is independent species. As an example, the sister group of the clade 1 of A. lemmi, evidently representing the ‘type clade’ of this species, is the clade 1 of A. kontrimavichusi. For A. kontrimavichusi, it is not known which one is the type clade. There is also fairly strong evidence for the non‐monophyly of Anoplocephaloides dentata (Galli‐Valerio, 1905)‐like species, although an earlier phylogeny suggested that this multispecies assemblage may be monophyletic. The results suggest a deep phylogenetic codivergence of Lemmus spp. and A. lemmi, primarily separating the two largely allopatric host and parasite species at the Kolyma River in east Siberia. There are also two allopatric sublineages within each main clade/species of A. lemmi and Lemmus, but the present distributions of the sublineages within the eastern L. trimucronatus and clade 1 of A. lemmi are not concordant. This discrepancy may be most parsimoniously explained by an extensive westward distributional shift of the easternmost parasite subclade. The results further suggest that the clade 1 of A. kontrimavichusi has diverged through a host shift from the precursor of L. trimucronatus to S. borealis.

Seasonal demography of a cyclic lemming population in the Canadian Arctic.

1. The causes of cyclical fluctuations in animal populations remain a controversial topic in ecology. Food limitation and predation are two leading hypotheses to explain small mammal population dynamics in northern environments. We documented the seasonal timing of the decline phases and demographic parameters (survival and reproduction) associated with population changes in lemmings, allowing us to evaluate some predictions from these two hypotheses. 2. We studied the demography of brown lemmings (Lemmus trimucronatus), a species showing 3- to 4-year population cycles in the Canadian Arctic, by combining capture-mark-recapture analysis of summer live-trapping with monitoring of winter nests over a 10-year period. We also examined the effects of some weather variables on survival. 3. We found that population declines after a peak occurred between the summer and winter period and not during the winter. During the summer, population growth was driven by change in survival, but not in fecundity or proportion of juveniles, whereas in winter population growth was driven by changes in late summer and winter reproduction. 4. We did not find evidence for direct density dependence on summer demographic parameters, though our analysis was constrained by the paucity of data during the low phase. Body mass, however, was highest in peak years. 5. Weather effects were detected only in early summer when lemming survival was positively related to snow depth at the onset of melt but negatively related to rainfall. 6. Our results show that high mortality causes population declines of lemmings during summer and fall, which suggests that predation is sufficient to cause population crashes, whereas high winter fecundity is the primary factor leading to population irruptions. The positive association between snow depth and early summer survival may be due to the protective cover offered by snow against predators. It is still unclear why reproduction remains low during the low phase.

Highly overlapping winter diet in two sympatric lemming species revealed by DNA metabarcoding.

Sympatric species are expected to minimize competition by partitioning resources, especially when these are limited. Herbivores inhabiting the High Arctic in winter are a prime example of a situation where food availability is anticipated to be low, and thus reduced diet overlap is expected. We present here the first assessment of diet overlap of high arctic lemmings during winter based on DNA metabarcoding of feces. In contrast to previous analyses based on microhistology, we found that the diets of both collared (Dicrostonyx groenlandicus) and brown lemmings (Lemmus trimucronatus) on Bylot Island were dominated by Salix while mosses, which were significantly consumed only by the brown lemming, were a relatively minor food item. The most abundant plant taxon, Cassiope tetragona, which alone composes more than 50% of the available plant biomass, was not detected in feces and can thus be considered to be non-food. Most plant taxa that were identified as food items were consumed in proportion to their availability and none were clearly selected for. The resulting high diet overlap, together with a lack of habitat segregation, indicates a high potential for resource competition between the two lemming species. However, Salix is abundant in the winter habitats of lemmings on Bylot Island and the non-Salix portion of the diets differed between the two species. Also, lemming grazing impact on vegetation during winter in the study area is negligible. Hence, it seems likely that the high potential for resource competition predicted between these two species did not translate into actual competition. This illustrates that even in environments with low primary productivity food resources do not necessarily generate strong competition among herbivores.

Evidence for Toxoplasma gondii in migratory vs. nonmigratory herbivores in a terrestrial arctic ecosystem

It is currently unclear how Toxoplasma gondii (Nicolle and Manceaux, 1908) persists in arctic tundra ecosystems in the absence of felid definitive hosts. To investigate potential transmission routes of T. gondii in a terrestrial arctic food web, we collected samples from two migratory herbivores, Ross’s Geese (Chen rossi (Cassin, 1861)) and Lesser Snow Geese (Chen caerulescens (L., 1758)), and from two resident herbivores, Nearctic brown lemmings (Lemmus trimucronatus (Richardson, 1825)) and collared lemmings (Dicrostonyx groenlandicus (Traill, 1823)), trapped at Karrak Lake, Nunavut, Canada. Antibodies were detected in 76 of 234 (32.4%) serum samples from Ross’s Geese and 66 of 233 (28.3%) serum samples from Lesser Snow Geese. We did not detect T. gondii antibodies in filter-paper eluate tested from thoracic fluid samples collected from 84 lemmings. We did not detect T. gondii DNA in brain tissue from these lemmings. Although a small sample size, our findings suggest that lemmings in this terrestrial arctic ecosystem are not exposed to, or infected with, the parasite. This suggests that oocysts are not introduced into the terrestrial arctic ecosystem at Karrak Lake via freshwater runoff from temperate regions. This study demonstrated that live adult arctic-nesting geese are exposed to T. gondii and therefore migratory herbivorous hosts are potential sources of T. gondii infection for predators in terrestrial arctic ecosystems.

Does lemming winter grazing impact vegetation in the Canadian Arctic?

In low-productivity environments such as the tundra, it has been proposed that regular, multi-annual population cycles of lemmings could be driven by winter food depletion in years of peak abundance. If lemming population dynamics is controlled by food resources, we predict that (1) winter grazing should negatively impact the abundance of food plants, (2) this impact should be proportional to lemming density and (3) high lemming winter grazing pressure should result in reduced plant growth during the following summer. We tested these predictions on Bylot Island, Nunavut, Canada, where two species of lemmings are present: the brown (Lemmus trimucronatus) and collared lemming (Dicrostonyx groenlandicus). We installed 16 exclosures in their preferred wintering habitat (snowbeds) and annually sampled plant biomass inside and outside exclosures at snow melt and at peak growth during the summers of 2009–2012, covering a full population cycle. Winter grazing had no impact on total vascular plant or moss biomass at snow melt in all years. Among plant families, only Caryophyllaceae, which was uncommon, showed a decline. In moss taxa, a negative effect was found on Polytrichum in only 1 year out of three. Overall, plant regrowth during the subsequent summer showed annual variation and tended to be reduced in the 2 years of high lemming abundance. However, this could be a consequence of summer grazing. Overall, the impact of lemming winter grazing on plants was weak and short-lived, even in years of high lemming abundance. Therefore, our results are not consistent with the hypothesis that food depletion during winter was the cause of the lemming decline following peak abundance at our study site. Other factors may limit lemming populations and prevent them from reaching densities high enough to exhaust their food resources.

Predation pressure by avian predators suggests summer limitation of small‐mammal populations in the Canadian Arctic

Predation has been suggested to be especially important in simple food webs and less productive ecosystems such as the arctic tundra, but very few data are available to evaluate this hypothesis. We examined the hypothesis that avian predators could drive the population dynamics of two cyclic lemming species in the Canadian Arctic. A dense and diverse suite of predatory birds, including the Snowy Owl (Bubo scandiacus), the Rough-legged Hawk (Buteo lagopus), and the Long-tailed Jaeger (Stercorarius longicaudus), inhabits the arctic tundra and prey on collared (Dicrostonyx groenlandicus) and brown (Lemmus trimucronatus) lemmings during the snow-free period. We evaluated the predation pressure exerted by these predators by combining their numerical (variation in breeding and fledgling numbers) and functional (variation in diet and daily consumption rates) responses to variations in lemming densities over the 2004-2010 period. Breeding density and number of fledglings produced by the three main avian predators increased sharply without delay in response to increasing lemming densities. The proportion of collared lemmings in the diet of those predators was high at low lemming density (both species) but decreased as lemming density increased. However, we found little evidence that their daily consumption rates vary in relation to changes in lemming density. Total consumption rate by avian predators initially increased more rapidly for collared lemming but eventually leveled off at a much higher value for brown lemmings, the most abundant species at our site. The combined daily predation rate of avian predators exceeded the maximum daily potential growth rates of both lemming species except at the highest recorded densities for brown lemmings. We thus show, for the first time, that predation pressure exerted without delay by avian predators can limit populations of coexisting lemming species during the snow-free period, and thus, that predation could play a role in the cyclic dynamic of these species in the tundra.

Patch use and vigilance by sympatric lemmings in predator and competitor-driven landscapes of fear

Prey living in risky environments can adopt a variety of behavioral tactics to reduce predation risk. In systems where predators regulate prey abundance, it is reasonable to assume that differential patterns of habitat use by prey species represent adaptive responses to spatial variation in predation. However, patterns of habitat use also reflect interspecific competition over habitat. Collared (Dicrostonyx groenlandicus) and brown (Lemmus trimucronatus) lemmings represent such a system and possess distinct upland tundra versus mesic meadow habitat preferences consistent with interspecific competition. Yet, we do not know whether this habitat preference might also reflect differences in predation risk or whether the two species differ in their behavioral tactics used to avoid predation. We performed experiments where we manipulated putative predation risk perceived by lemmings by increasing protective cover in upland and meadow habitats while we recorded lemming activity and behavior. Both lemming species preferentially used cover more than open patches, but Dicrostonyx was more vigilant than Lemmus. Both species also constrained their activity to protective patches in upland and meadow habitats, but during different periods of the day. Use of cover and vigilance were independent of habitat, suggesting that both species live in a fearsome but flattened landscape of fear at Walker Bay (Nunavut, Canada), and that their habitat preference is a consequence of competition rather than predation risk. Future studies aiming to map the contours of fear in multi-prey–predator systems should consider how predation and competition interact to modify prey species’ habitat preference, patch use, and vigilance.

Landscapes of fear or competition? Predation did not alter habitat choice by Arctic rodents

In systems where predation plays a key role in the dynamics of prey populations, such as in Arctic rodents, it is reasonable to assume that differential patterns of habitat use by prey species represent adaptive responses to spatial variation in predation. However, habitat selection by collared (Dicrostonyx groenlandicus) and brown (Lemmus trimucronatus) lemmings depends on intra- and inter-specific densities, and there has been little agreement on the respective influences of food abundance, predators, and competition for habitat on lemming dynamics. Thus, we investigated whether predation affected selection of sedge-meadow versus upland tundra by collared lemmings in the central Canadian Arctic. We first controlled for the effects of competition on lemming habitat selection. We then searched for an additional signal of predation by comparing habitat selection patterns between 12 control plots and one large grid where lemmings were protected from predators by fencing in 1996 and 1997, but not during 5 subsequent years when we monitored habitat use in the grid as well as in the control plots. Dicrostonyx used upland preferentially over meadows and was more numerous in 1996 and 2011 than in other sample years. Lemmus was also more abundant in 1996 than in subsequent years, but its abundance was too low in the exclosure to assess whether exclusion of predators influenced its habitat selection. Contrary to the effects of competition, predation had a negligible impact on the spatial dynamics of Dicrostonyx, at least during summer. These results suggest that any differences in predation risk between the two habitats have little direct influence on the temporal dynamics of Dicrostonyx even if induced through predator-prey cycles.

The effect of snow cover on lemming population cycles in the Canadian High Arctic

Rising temperatures and changes in the precipitation regime will have a strong impact on the quality of the snow cover in the Arctic. A snow cover of good quality protecting lemmings from cold temperatures and predators is thought to be an important factor for maintaining the cyclic dynamic of their populations in the tundra. We examined if the characteristics of annual fluctuations (amplitude and shape of phases) in brown lemming (Lemmus trimucronatus) density could be determined by snow depth, snow density, sub-nivean temperature and persistence of snow. Using an 18-year time series of brown lemming abundance on Bylot Island in the Canadian Arctic, we tested if snow variables could explain the residual variation between the observed lemming density and the one predicted by models where cyclicity had been accounted for. Our analysis provides support for the hypothesis that snow cover can affect the amplitude and possibly also the periodicity of lemming population cycles in the High Arctic. Summer abundance of brown lemmings was higher following winters with a deep snow cover and a low-density snow pack near the ground but was unaffected by the date of establishment or melting and duration of the snow cover. Two snow variables showed a temporal trend; mean winter snow depth tended to increase and date of establishment of the hiemal threshold occurred earlier over time. These temporal trends, which should be favourable to lemmings, may explain why healthy population cycles have apparently been maintained at our study site contrary to other Arctic sites.

Some Observations of Short-eared Owl, <em>Asio flammeus</em>, Ecology on Arctic Tundra, Yukon, Canada

We investigated nesting behavior, food habits, and interspecific interactions of Short-eared Owls (Asio flammeus) within an arctic tundra raptor community on Herschel Island and Komakuk Beach, northern Yukon, Canada. Short-eared Owls were the least common nesting raptor. We found only three nests, all on Herschel Island. All nests were on relatively elevated sites with fairly substantial vegetative cover. All nests failed in the egg stage, from a combination of human disturbance and possible predation by Arctic Fox (Vulpes lagopus) or Red Fox (Vulpes vulpes). Short-eared Owls nested only in years when small rodent densities were at least 4 to 5 individuals per hectare in the spring. Short-eared Owls ate Northern Collared Lemmings (Dicrostonyx groenlandicus), Brown Lemmings (Lemmus trimucronatus), and Tundra Voles (Microtus oeconomus) almost exclusively, without clear selectivity. Peregrine Falcons (Falco peregrinus) killed two adult Short-eared Owls. In northern Yukon, the Short-eared Owl remains an uncommon summer resident and uses the region as a migration route. Spring rodent densities and interspecific predation are prominent limiting factors, and human disturbance also limits nesting success. We recommend restricting access to most tundra areas during periods when the birds are mating, initiating nesting, and incubating eggs. We recommend that human infrastructure be designed so that it cannot support novel nesting (and therefore local range expansion) by other nesting raptors that compete with and prey on Short-earned Owls.