Movement patterns of a specialist predator,the weasel<Emphasis Type="Italic">Mustela nivalis</Emphasis> exploiting asynchronous cyclic field vole<Emphasis Type="Italic">Microtus agrestis</Emphasis> populations

We investigated habitat selection and movement characteristics of male weaselsMustela nivalis Linnaeus, 1766 during the breeding season through radio-telemetry in Kielder Forest (KF) in order to assess how weasel movement is influenced by prey dynamics, mate searching and predation risk, and whether the scale of weasel movement corresponds to the spatial scale of the asynchronous, multi-annual vole population cycles observed in KF. Weasels used habitats with a high proportion of grass cover to a much larger extend than habitats with less grass cover and moved through the latter habitats faster and / or straighter. Habitats with high amounts of grass cover also had the highest field vole abundance, although total rodent abundance did not differ between habitats. The selection of this habitat by weasels might reflect weasels preferring field voles as prey or avoiding habitats with little grass cover and high intraguild predation risk. Five out of 8 male weasels radio-tracked had low day-to-day site fidelity and moved between different clear cuts. Three other males were resident in a single clear cut. This variation may reflect mate searching by male weasels. The observation that most weasels (5 out of 8) roamed over large areas and the scale of their dispersal potential suggests, that if they regulated vole populations, they should have a greater synchronising effect on the spatial scale of vole population dynamics than what is observed in vole populations in KF.     

Landscape effects on temporal and spatial properties of vole population fluctuations

Populations of northern small rodents have previously been observed to fluctuate in spatial synchrony over distances ranging from tens to hundreds of kilometers between sites. It has been suggested that this phenomenon is caused by common environmental perturbations, mobile predators or dispersal movements. However, very little focus has been given to how the physical properties of the geographic area over which synchrony occurs, such as landscape composition and climate, affect spatial population dynamics. This study reports on the spatial and temporal properties of vole population fluctuations in two areas of western Finland: one composed of large interconnected areas of agricultural farmland interspersed by forests and the other highly dominated by forest areas, containing more isolated patches of agricultural land. Furthermore, the more agricultural area exhibits somewhat milder winters with less snow than the forested area. We found the amplitude of vole cycles to be essentially the same in the two areas, suggesting that the relative amount of predation on small rodents by generalist versus specialist predators is similar in both areas. No seasonal differences in the timing of synchronization were observable for Microtus voles, whereas bank vole populations in field habitats appeared to become synchronized primarily during winter. Microtus populations in field habitats exhibited smaller spatial variation and a higher degree of synchrony in the more continuous agricultural landscape than in the forest-dominated landscape. We suggest that this inter-areal difference is due to differences in the degree of inter-patch connectivity, with predators and dispersal acting as the primary synchronizing agents. Bank vole populations in field habitats were more synchronized within the forest-dominated landscape, most likely reflecting the suitability of the inter-patch matrix and the possibility of dispersal. Our study clearly indicates that landscape composition needs to be taken into account when describing the spatial properties of small rodent population dynamics.     

Density-dependent dispersal and spatial population dynamics

The synchronization of the dynamics of spatially subdivided populations is of both fundamental and applied interest in population biology. Based on theoretical studies, dispersal movements have been inferred to be one of the most general causes of population synchrony, yet no empirical study has mapped distance-dependent estimates of movement rates on the actual pattern of synchrony in species that are known to exhibit population synchrony. Northern vole and lemming species are particularly well-known for their spatially synchronized population dynamics. Here, we use results from an experimental study to demonstrate that tundra vole dispersal movements did not act to synchronize population dynamics in fragmented habitats. In contrast to the constant dispersal rate assumed in earlier theoretical studies, the tundra vole, and many other species, exhibit negative density-dependent dispersal. Simulations of a simple mathematical model, parametrized on the basis of our experimental data, verify the empirical results, namely that the observed negative density-dependent dispersal did not have a significant synchronizing effect.     

Emigration to new habitats by voles: the cost of dispersal paradox

We tested the hypothesis that dispersal and philopatry are components of a mixed evolutionarily stable strategy (ESS). The hypothesis predicts that fitness of dispersers should be equal to that of philopatric individuals. Alternatively, fitness of dispersers could be lower (the resident fitness hypothesis) or greater (the cost of dispersal hypothesis) than that of philopatric individuals. We compared fitness of individuals that moved to new habitats (emigrants) and those that remained within habitat boundaries (residents) in populations of the prairie vole, Microtus ochrogaster, and the meadow vole, M. pennsylvanicus. We established vole populations in four enclosures (). Within each enclosure, voles were free to move between four types of habitats that varied in the availability of supplemental food and the amount of vegetative cover. We analysed two fitness components: the survival rates of all individuals, and pregnancy rates of females. Our study showed that emigrants generally had greater fitness than residents and that the difference in fitness was habitat dependent (i.e. was greater when individuals were emigrating from low-quality habitats than from high-quality habitats). High-food, high-cover habitats were the only habitat types for which fitness of emigrants was lower than that of residents. Similar patterns occurred in both prairie voles and meadow voles. Our results support the cost of dispersal hypothesis.     

Habitat composition as a determinant of reproductive success of Tengmalm's owls under fluctuating food conditions

The effect of landscape composition on the breeding success of vole-eating Tengmalm's owl ( Aegolius funereus ) was studied in western Finland at five different spatial scales (250–4000 m) around the nests during two consecutive three-year population cycles of voles. Landscape composition had strongest effects on owl breeding in the decrease phase of vole cycles. Significant variation in owl breeding occurred along the productivity gradient from farmland predominated areas to barren hinterland. Owls tended to produce earlier clutches on territories predominated by agricultural areas in increasing vole years. A similar trend was observed in the decreasing phase of the vole cycle; owls breeding on barren hinterland seemed to delay breeding compared to owls breeding near agricultural areas. Surprisingly, nestling survival and fledgling production in the decreasing phase declined steeply with increasing proportion of farmland. Clutch size was not significantly related to landscape composition. The number of fledglings decreased with increases in clear-cut and sapling areas in the decrease phase. During the declining years of vole abundance nestling survival increased from western farmland areas towards the eastern outlying district. These results indicate sudden summer decline of vole populations on farmland predominated habitats. This is probably due to that the number of vole-eating predators, and hence their impact on vole populations is apparently higher in farmland areas than on forested hinterland. This finding gives support for the 'spill-over' hypothesis, which states that predators and their exploitation tends to 'spill over' from luxuriant habitats to the barren habitats.     

HOW DOES POLLEN VERSUS SEED DISPERSAL AFFECT NICHE EVOLUTION?

In heterogeneous landscapes, the genetic and demographic consequences of dispersal influence the evolution of niche width. Unless pollen is limiting, pollen dispersal does not contribute directly to population growth. However, by disrupting local adaptation, it indirectly affects population dynamics. We compare the effect of pollen versus seed dispersal on the evolution of niche width in heterogeneous habitats, explicitly considering the feedback between maladaptation and demography. We consider two scenarios: the secondary contact of two subpopulations, in distinct, formerly isolated habitats, and the colonization of an empty habitat with dispersal between the new and ancestral habitat. With an analytical model, we identify critical levels of genetic variance leading to niche contraction (secondary contact scenario), or expansion (new habitat scenario). We confront these predictions with simulations where the genetic variance freely evolves. Niche contraction occurs when habitats are very different. It is faster as total gene flow increases or as pollen predominates in overall gene flow. Niche expansion occurs when habitat heterogeneity is not too high. Seed dispersal accelerates it, whereas pollen dispersal tends to retard it. In both scenarios very high seed dispersal leads to extinction. Overall, our results predict a wider niche for species dispersing seeds more than pollen.     

Source–sink dynamics: how sinks affect demography of sources

Models of source–sink population dynamics have to make assumptions about whether, and eventually how, demographic parameters in source habitats are dependent on the demography in sink habitats. However, the empirical basis for making such assumptions has been weak. Here we report a study on experimental root vole populations, where estimates of demographic parameters were contrasted between source patches in source–sink (treatment) and source–source systems (control). In the presence of a sink patch (simulated by a pulsed removal of immigrants), source‐patch populations failed to increase over the breeding season, mainly due to a high spatially density‐dependent dispersal rate from source to sink patches. The per capita recruitment rate was almost two times higher in source–sink than in the source–source systems, but this did not compensate for the loss rate due to dispersal from source to sink patches. Sex ratio in the source–sink systems became less female biased, probably as a result of an enhanced frequency of dispersal movements in females. Good knowledge of the degree of density‐and habitat‐dependent dispersal is critical for predicting the dynamics of source–sink populations.     

Heterogeneous landscapes and the role of refuge on the population dynamics of a specialist predator and its prey

How, and where, a prey species survives predation by a specialist predator during low phases of population fluctuations or a cycle, and how the increase phase of prey population is initiated, are much-debated questions in population and theoretical ecology. The persistence of the prey species could be due mainly to habitats that act as refuges from predation and/or due to anti-predatory behaviour of individuals. We present models for the former conjecture in two (and three) habitat systems with a specialist predator and its favoured prey. The model is based on dispersal of prey between habitats with high reproductive output but high risk of predation, and less productive habitats with relatively low risk of predation. We illustrate the predictions of our model using parameters from one of the most intriguing vertebrate predator–prey systems, the multi-annual population cycles of boreal voles and their predators. We suggest that cyclic population dynamics could result from a sequence of extinction and re–colonization events. Field voles (Microtus agrestis), a key vole species in the system, can be hunted to extinction in their preferred meadow habitat, but persist in sub-optimal wet habitats where their main predator, the least weasel (Mustela nivalis nivalis) has a low hunting efficiency. Re–colonization of favourable habitats would occur after the predator population crashes. At the local scale, the model suggests that the periodicity and amplitude of population cycles can be strongly influenced by the relative availability of risky and safe habitats for the prey. Furthermore, factors like intra-guild predation may lead to reduced predation pressure on field voles in sub-optimal habitats, which would act as a refuge for voles during the low phase of their population cycles. Elasticity analysis suggested that our model is quite robust to changes in most parameters but sensitive to changes in the population dynamics of field voles in the optimal grassland habitat, and to the maximum predation rate of weasels.     

Linking demography and host dispersal to Trichuris arvicolae distribution in a cyclic vole species

Spatial structure in the distribution of pathogen infection can influence both epidemiology and host-parasite coevolutionary processes. It may result from the spatial heterogeneity of intrinsic and extrinsic factors, or from the local population dynamics of hosts and parasites. In this study, we investigated the effects of landscape, host dispersal and demography (population abundance and phase of the fluctuation) on the distribution of a gastro-intestinal nematode Trichuris arvicolae in the fossorial water vole Arvicola terrestris sherman. This rodent exhibits outbreaks occurring regularly in Franche-Comté (France). Thirteen out-of-phase populations were studied in autumn 2003. They exhibited highly different T. arvicolae prevalences. The heterogeneity in prevalences was not explained by population structure, landscape or vole abundance, but by the phase of the vole population fluctuations. Populations at the end of the high density phase showed null prevalence whereas populations in increase or outbreak phases exhibited higher prevalences. Population genetic analyses based on microsatellites revealed significant differentiation between vole populations, and higher dispersal rates of young voles compared with old ones. These younger individuals were also infected more frequently than older voles. This suggested a role of host dispersal in the distribution of T. arvicolae. However, there was a strong discrepancy between the spatial patterns of prevalence and of host genetics or demographic phase. Genetic differentiation and differences in demographic phase exhibited significant spatial autocorrelations whereas prevalence did not. We concluded that the distribution of T. arvicolae is influenced by vole dispersal, although this effect might be overwhelmed by local adaptation processes or environmental conditions.     

Sperm DNA and sex chromosome differences between two geographical populations of the creeping vole, Microtus oregoni

The relative DNA content of the "O" and Y chromosome-bearing sperm is presented for the creeping vole, Microtus oregoni. The animals had been trapped in Oregon and in Washington State. The two populations had very similar autosomal chromosome relationships but differed greatly in the size of their X chromosome (which is not carried by vole sperm) and in their Y chromosome. The greater size and banding differences of the Y chromosome of the Washington State vole compared to the Oregon vole paralleled the greater differences in sperm DNA between the Y-bearing sperm and the sperm carrying no sex chromosome (O). The actual DNA differences between O and Y sperm was 12.5% for the sperm from the Washington State voles and 9.1% for sperm from the Oregon voles. The difference in sperm DNA content (12.5%) for Washington State voles was far greater than the difference shown for other voles or other mammals.     

Population dynamics in two-patch environments: Some anomalous consequences of an optimal habitat distribution

The effect of dispersal on population size and stability is explored for a population that disperses passively between two discrete habitat patches. Two basic models are considered. In the first model, a single population experiences density-dependent growth in both patches. A graphical construction is presented which allows one to determine the spatial pattern of abundance at equilibrium for most reasonable growth models and rates of dispersal. It is shown under rather general conditions that this equilibrium is unique and globally stable. In the second model, the dispersing population is a food-limited predator that occurs in both a source habitat (which contains a prey population) and a sink habitat (which does not). Passive dispersal between source and sink habitats can stabilize an otherwise unstable predator-prey interaction. The conditions allowing this are explored in some detail. The theory of optimal habitat selection predicts the evolutionarily stable distribution of a population, given that individuals can freely move among habitats so as to maximize individual fitness. This theory is used to develop a heuristic argument for why passive dispersal should always be selectively disadvantageous (ignoring kin effects) in a spatially heterogeneous but temporally constant environment. For both the models considered here, passive dispersal may lead to a greater number of individuals in both habitats combined than if there were no dispersal. This implies that the evolution of an optimal habitat distribution may lead to a reduction in population size; in the case of the predator-prey model, it may have the additional effect of destabilizing the interaction. The paper concludes with a discussion of the disparate effects habitat selection might have on the geographical range occupied by a species.     

Dispersal,kin competition,and the ideal free distribution in a spatially heterogeneous population

In this paper, we reanalyze simple models of the evolution of dispersal in a heterogeneous landscape. Previous analyses concluded that without temporal variability, dispersal can evolve only if it is not costly and if it is conditional on the habitat. If both conditions hold, these models predict that selection on dispersal should lead to balanced dispersal between habitats (the number of immigrants equals the number of emigrants in each habitat). To evaluate the generality of these conclusions, we extended the analysis of these models to finite populations. This requires us to establish fitness measures for finite class-structured populations. These fitness measures allow us to take kin competition into account. Our analysis shows that even without temporal variability, conditional dispersal and the absence of a dispersal cost are not necessary conditions for dispersal to evolve. In the absence of a dispersal cost, we predict that selection on conditional dispersal will always lead to panmixia and not simply to balanced dispersal. When dispersal is costly, we show that the ideal free distribution (IFD) and balanced dispersal do not occur. Our results show that the deviations from IFD are of the order of the dispersal cost. We propose an approach to test our predictions.     

Winter herbivory by voles during a population peak: the relative importance of local factors and landscape pattern

1. We studied the relative role of local habitat variables and landscape pattern on vole–plant interactions in a system with grey-sided voles ( Clethrionomys rufocanus (Sund.)) and their favourite winter food plant, bilberry ( Vaccinium myrtillus L.). The study was conducted during a vole peak year (1992–93) in a tundra area in northern Norway.
2. Using Mantel statistics we were able to separate the direct effects of the spatial patterning of habitats and the indirect effects due to spatial aggregations of similar habitats.
3. Results indicate that knowledge about the explicit spatial patterning of patches does not improve our understanding of the system. Instead, two local factors, vegetation height and bilberry biomass, explained more than 50% of the variation in cutting intensity in winter (defined as the proportion of above-ground shoots cut). Increasing vegetation height increased, and increasing bilberry biomass decreased, the cutting intensity.
4. The conclusion that grey-sided voles are able to distribute themselves relative to habitat quality was also partially supported by our estimated over-winter persistence by voles in the various habitats. Vole persistence was uncorrelated with vegetation height, the important predictor of autumn vole density, but tended to correlate with the deviation from the relation between vegetation height and autumn vole density. This conforms to the expectations from the theory of ideal-free habitat distribution.
5. The cue for vole habitat choice, i.e. vegetation height, indicates that either predation or freezing risk is important for voles when selecting over-wintering habitat.     

Evidence for different drivers behind long-term decline and depression of density in cyclic voles

Decline and long-term depression of mean densities of the grey-sided vole (Myodes rufocanus) and the field vole (Microtus agrestis) have occurred in managed forest landscapes of Sweden since the 1970s. Generally poor over-winter survival during a period with mild winters suggested a common climatic driver, but other explanations exist. Here we explore the response of the grey-sided vole, preferring forested habitats, and the field vole, preferring open habitats, to clear-cutting of old forest in Sweden. The cumulated impact from long-term clear-cutting explained local disappearances of the grey-sided vole. Maintained connectivity of old forest to stone fields was important for local population survival, since no such populations disappeared. For the grey-sided vole, it is probable that climate is not the dominating driver due to different timing of the decline in our study area. Instead, habitat loss is concluded as being a potential cause of the decline in mean density and depression of grey-sided vole densities. The long-lasting depression of field vole densities, despite favourable landscape changes, suggests action of another strong driver. A recent field vole recovery, essentially back to pre-decline densities and distribution, coincided with favourable winter/snow conditions, suggesting a climatic driver in this case.     

A spatially explicit model of sex ratio evolution in response to sex-biased dispersal

Sex-biased dispersal occurs in all seed plants and many animal species. Theoretical models have shown that sex-biased dispersal can lead to evolutionarily stable biased sex ratios. Here, we use a spatially explicit chessboard model to simulate the evolution of sex ratio in response to sex-biased dispersal range and sex-biased dispersal rate. Two life cycles are represented in the model: one in which both sexes disperse before mating (DDM), the other in which males disperse before mating and mated females or zygotes disperse after mating (DMD). Model parameters include factors like dispersal rate, dispersal range, number of individuals per patch, and habitat heterogeneity.When dispersal range is sex biased, we find that, in a homogeneous environment, the sex ratio is generally biased towards the sex that disperses more widely (sex ratio range: 0.47–0.52). In a heterogeneous environment, the sex ratio is generally biased towards the more dispersive sex in good habitats, and towards the less dispersive sex in poor habitats (sex ratio range: 0–1). This is opposite to the effect of sex-biased dispersal rate, which favours the production of the more dispersive sex in poor habitats and the less dispersive sex in good habitats (sex ratio range: 0–1). To allow for a comparison with theoretical predictions, data concerning sex-biased dispersal and habitat-dependent sex ratios should thus incorporate information about the spatial scale of both dispersal and environmental heterogeneity.     

Breeding dispersal of Eurasian kestrels Falco tinnunculus under temporally fluctuating food abundance

Costs and benefits of dispersal can vary in space and time, depending on environmental factors and individual state. Plastic, condition‐dependent dispersal strategies, in which individuals rely on external cues such as food abundance to adjust their dispersal distances, are therefore expected to evolve in temporally fluctuating environments. We examined factors affecting breeding dispersal distances in Eurasian kestrels Falco tinnunculus subsisting on multi‐annually and cyclically fluctuating voles as their main food. We attempted to avoid traditional bias in dispersal studies by having large study areas and by taking detection probabilities into account. We observed 320 dispersal events of male and 215 events of female kestrels from our study areas in western Finland during 24 yr. After correcting for distance‐specific detection probability, the estimates of mean dispersal distances increased two‐fold being still clearly higher for females than males. Vole abundance in the spring of settlement was more important in determining average dispersal distances than vole abundance in the previous autumn. At the population level (cross‐sectional model), both males and females dispersed longer distances when the spring abundance of their main food (voles) was low compared to when it was abundant, as predicted by the food depletion hypothesis. At the individual level (longitudinal model), only females responded to the food situation by dispersing more when food abundance was low in the spring of settlement. Females also dispersed longer when vole abundance in the previous autumn had been high. Individual males did not respond to vole abundance, which implies that the population level response in males might have been caused by long‐distance dispersers, which breed in the study area only in good vole years. Our results show that the dispersal distances of kestrels at northern latitudes depend both on individual properties (gender, age, and possibly individual tendency to disperse) and environmental conditions (temporal variation in main food abundance).     

Not all free-living microorganisms have cosmopolitan distributions – the case of Nebela (Apodera) vas Certes (Protozoa: Amoebozoa: Arcellinida)

Aim  To review and critically assess the evidence that the testate amoeba species Nebela vas does not have a cosmopolitan distribution, in contradiction to the paradigm of microbial distribution that 'everything is everywhere'.
Location  Terrestrial and wetland habitats world-wide.
Methods  Relevant data were assembled on the morphology, ecology and global geographical distribution of N. vas from a comprehensive literature review of published original records. The data were collated, analysed and summarized. The roles of long-term and short-term agents of dispersal are discussed.
Results  A clear and repeated pattern has been elucidated of a microbial species, with a distinctive and unmistakeable morphology, that inhabits acid, damp terrestrial and wetland habitats in the southern cool-temperate and sub-Antarctic zones – including similar high-altitude habitats in the Tropics. It is almost entirely confined to the Gondwanaland continents and Southern Hemisphere islands. It is definitively absent from Holarctic regions. It is proposed that the continental distribution of N. vas is a consequence of continental drift following its original speciation in the Mesozoic or earlier, whereas its distribution on sub-Antarctic islands (glaciated in the Pleistocene) has been effected by dispersal from South America by wind around the Southern Ocean.
Main conclusion  Nebela vas is a proven instance of a microbial species that does not have a cosmopolitan distribution.     

Spatio-temporal patterns of habitat use in voles and shrews modified by density, season and predators

1.?Although the intrinsic habitat preferences of a species can be considered to be fixed, the realized habitat use depends on the prevailing abiotic and biotic conditions. Often the core habitats are occupied by dense and stable populations, while marginal habitats become occupied only at times of high density. In a community of interacting species, habitat uses of different species become inter-related, for example an increased density of a strong competitor forcing a weaker competitor to use more marginal habitats. 2.?We studied the spatio-temporal distribution patterns of three common small mammal species, the bank vole Myodes glareolus; the field vole Microtus agrestis; and the common shrew Sorex araneus, in a 4-year trapping study carried out on six large islands, each containing a mixture of three main habitat types (forest, field and clear-cut). We experimentally released least weasels (Mustela n. nivalis) to some of the islands to see how the focal species respond to increased predation pressure. 3.?Both vole species were largely restricted to their core habitats (bank voles to forests and field voles to fields) at times of low population density. With increasing density, the relative habitat use of both species increased in the clear-cut areas. The common shrew was a generalist in its habitat use at all population densities. 4.?The release of the weasels changed the habitat use of all study species. 5.?The vole species showed a stronger aggregated pattern than the common shrew, especially at low population density. The vole aggregations remained in the same localities between seasons, except in the case of bank voles after the weasels were released. 6.?Bank voles and field voles avoided each other at high density. 7.?We conclude that intrinsically differential habitat requirements and flexibility to modify habitat use facilitate the coexistence of the two competing vole species in mosaic landscapes consisting of boreal forests and open habitats.     

Notonecta exhibit threat-sensitive,predator-induced dispersal

Dispersal is a central process determining community structure in heterogeneous landscapes, and species interactions within habitats may be a major determinant of dispersal. Although the effects of species interactions on dispersal within habitats have been well studied, how species interactions affect the movement of individuals between habitats in a landscape has received less attention. We conducted two experiments to assess the extent to which predation risk affects dispersal from an aquatic habitat by a flight-capable semi-aquatic insect (Notonecta undulata). Exposure to non-lethal (caged) fish fed conspecifics increased dispersal rates in N. undulata. Moreover, dispersal rate was positively correlated with the level of risk imposed by the fish; the greater the number of notonectids consumed by the caged fish, the greater the dispersal rate from the habitat. These results suggest that risk within a habitat can affect dispersal among habitats in a landscape and thus affect community structure on a much greater scale than the direct effect of predation itself.     

Evolution of the distribution of dispersal distance under distance‐dependent cost of dispersal

Abstract We analyse the evolution of the distribution of dispersal distances in a stable and homogeneous environment in one‐ and two‐dimensional habitats. In this model, dispersal evolves to avoid the competition between relatives although some cost might be associated with this behaviour. The evolutionarily stable dispersal distribution is characterized by an equilibration of the fitness gains among all the different dispersal distances. This cost‐benefit argument has heuristic value and facilitates the comprehension of results obtained numerically. In particular, it explains why some minimal or maximal probability of dispersal may evolve at intermediate distances when the cost of dispersal function is an increasing function of distance. We also show that kin selection may favour long range dispersal even if the survival cost of dispersal is very high, provided the survival probability does not vanish at long distances.