Comparison of baiting strategies in common vole management.

BACKGROUND: Worldwide, pest rodents can cause extensive damage to agriculture, forestry, food storage, and infrastructure and pose a risk to public health and livestock due to the spread of zoonotic pathogens. In Europe, the most common pest rodent species is the common vole (Microtus arvalis). Management during periodic outbreaks largely relies on rodenticidal bait with zinc phosphide. Efficient baiting with rodenticides or possibly anti-fertility products in the future require baiting methods that allow a sufficient proportion of the population to consume an effective dose of bait. We used a bait with the quantitative marker ethyl-iophenoxic acid (Et-IPA) to evaluate baiting strategies in enclosure experiments. This wheat-based bait with Et-IPA was placed in bait boxes or directly into the tunnel system entrances in different seasons and common vole abundances. Voles were live-trapped, individually marked and blood samples were collected to relate Et-IPA blood residues to bait uptake. RESULTS: The percentage of animals consuming bait was not heavily affected by the baiting strategy but voles had higher Et-IPA blood residues if tunnel baiting was used in autumn and if bait boxes were used in winter. Non-reproductive as well as lighter animals tended to have higher Et-IPA blood residues than reproductive individuals, whereas sex had no effect. Population density had a negative effect on the probability of residues present as well as on Et-IPA blood concentration. CONCLUSION: The results of this study might help to improve baiting techniques to manage overabundant rodent pest species regardless of the compounds to be delivered. © 2024 Julius Kühn-Institut. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Population cycles and outbreaks of small rodents: ten essential questions we still need to solve.

Most small rodent populations in the world have fascinating population dynamics. In the northern hemisphere, voles and lemmings tend to show population cycles with regular fluctuations in numbers. In the southern hemisphere, small rodents tend to have large amplitude outbreaks with less regular intervals. In the light of vast research and debate over almost a century, we here discuss the driving forces of these different rodent population dynamics. We highlight ten questions directly related to the various characteristics of relevant populations and ecosystems that still need to be answered. This overview is not intended as a complete list of questions but rather focuses on the most important issues that are essential for understanding the generality of small rodent population dynamics.

Biodiversity-multifunctionality relationships depend on identity and number of measured functions.

Biodiversity ensures ecosystem functioning and provisioning of ecosystem services, but it remains unclear how biodiversity-ecosystem multifunctionality relationships depend on the identity and number of functions considered. Here, we demonstrate that ecosystem multifunctionality, based on 82 indicator variables of ecosystem functions in a grassland biodiversity experiment, increases strongly with increasing biodiversity. Analysing subsets of functions showed that the effects of biodiversity on multifunctionality were stronger when more functions were included and that the strength of the biodiversity effects depended on the identity of the functions included. Limits to multifunctionality arose from negative correlations among functions and functions that were not correlated with biodiversity. Our findings underline that the management of ecosystems for the protection of biodiversity cannot be replaced by managing for particular ecosystem functions or services and emphasize the need for specific management to protect biodiversity. More plant species from the experimental pool of 60 species contributed to functioning when more functions were considered. An individual contribution to multifunctionality could be demonstrated for only a fraction of the species.

A comparison of the strength of biodiversity effects across multiple functions.

In order to predict which ecosystem functions are most at risk from biodiversity loss, meta-analyses have generalised results from biodiversity experiments over different sites and ecosystem types. In contrast, comparing the strength of biodiversity effects across a large number of ecosystem processes measured in a single experiment permits more direct comparisons. Here, we present an analysis of 418 separate measures of 38 ecosystem processes. Overall, 45 % of processes were significantly affected by plant species richness, suggesting that, while diversity affects a large number of processes not all respond to biodiversity. We therefore compared the strength of plant diversity effects between different categories of ecosystem processes, grouping processes according to the year of measurement, their biogeochemical cycle, trophic level and compartment (above- or belowground) and according to whether they were measures of biodiversity or other ecosystem processes, biotic or abiotic and static or dynamic. Overall, and for several individual processes, we found that biodiversity effects became stronger over time. Measures of the carbon cycle were also affected more strongly by plant species richness than were the measures associated with the nitrogen cycle. Further, we found greater plant species richness effects on measures of biodiversity than on other processes. The differential effects of plant diversity on the various types of ecosystem processes indicate that future research and political effort should shift from a general debate about whether biodiversity loss impairs ecosystem functions to focussing on the specific functions of interest and ways to preserve them individually or in combination.

To breed, or not to breed? Predation risk induces breeding suppression in common voles.

Breeding suppression hypothesis (BSH) predicts that, in several vole species, females will suppress breeding in response to high risk of mustelid predation; compared to breeding females, suppressing females would gain higher chances of survival. Seminal evidence for BSH was obtained in the laboratory, but attempts to replicate breeding suppression under field conditions were less conclusive. We tested whether breeding suppression occurs in common voles (Microtus arvalis), and how population density and predation risk combined affect voles' reproductive activity. We found that, in contrast to males, female common voles suppress reproductive activity when faced with high predation risk. Population size was not reduced despite breeding suppression. A model of the interaction between predation risk and population density revealed that predator-induced breeding suppression depends on the density of conspecifics. We concluded that breeding suppression is a viable adaptation only at low vole densities, when per capita predation risk is high. Finally, we identified the key issues of experimental design required for the consistency of future studies on breeding suppression.

Bottom-up effects of plant diversity on multitrophic interactions in a biodiversity experiment.

Biodiversity is rapidly declining, and this may negatively affect ecosystem processes, including economically important ecosystem services. Previous studies have shown that biodiversity has positive effects on organisms and processes across trophic levels. However, only a few studies have so far incorporated an explicit food-web perspective. In an eight-year biodiversity experiment, we studied an unprecedented range of above- and below-ground organisms and multitrophic interactions. A multitrophic data set originating from a single long-term experiment allows mechanistic insights that would not be gained from meta-analysis of different experiments. Here we show that plant diversity effects dampen with increasing trophic level and degree of omnivory. This was true both for abundance and species richness of organisms. Furthermore, we present comprehensive above-ground/below-ground biodiversity food webs. Both above ground and below ground, herbivores responded more strongly to changes in plant diversity than did carnivores or omnivores. Density and richness of carnivorous taxa was independent of vegetation structure. Below-ground responses to plant diversity were consistently weaker than above-ground responses. Responses to increasing plant diversity were generally positive, but were negative for biological invasion, pathogen infestation and hyperparasitism. Our results suggest that plant diversity has strong bottom-up effects on multitrophic interaction networks, with particularly strong effects on lower trophic levels. Effects on higher trophic levels are indirectly mediated through bottom-up trophic cascades.

Diversity promotes temporal stability across levels of ecosystem organization in experimental grasslands.

The diversity-stability hypothesis states that current losses of biodiversity can impair the ability of an ecosystem to dampen the effect of environmental perturbations on its functioning. Using data from a long-term and comprehensive biodiversity experiment, we quantified the temporal stability of 42 variables characterizing twelve ecological functions in managed grassland plots varying in plant species richness. We demonstrate that diversity increases stability i) across trophic levels (producer, consumer), ii) at both the system (community, ecosystem) and the component levels (population, functional group, phylogenetic clade), and iii) primarily for aboveground rather than belowground processes. Temporal synchronization across studied variables was mostly unaffected with increasing species richness. This study provides the strongest empirical support so far that diversity promotes stability across different ecological functions and levels of ecosystem organization in grasslands.

Foraging patterns of voles at heterogeneous avian and uniform mustelid predation risk.

Temporal variation of antipredatory behavior and a uniform distribution of predation risk over refuges and foraging sites may create foraging patterns different from those anticipated from risk in heterogenous habitats. We studied the temporal variation in foraging behavior of voles exposed to uniform mustelid predation risk and heterogeneous avian predation risk of different levels induced by vegetation types in eight outdoor enclosures (0.25 ha). We manipulated mustelid predation risk with weasel presence or absence and avian predation risk by reducing or providing local cover at experimental food patches. Foraging at food patches was monitored by collecting giving-up densities at artificial food patches, overall activity was automatically monitored, and mortality of voles was monitored by live-trapping and radiotracking. Voles depleted the food to lower levels in the sheltered patches than in the exposed ones. In enclosures with higher avian predation risk caused by lower vegetation height, trays were depleted to lower levels. Unexpectedly, voles foraged in more trays and depleted trays to lower levels in the presence of weasels than in the absence. Weasels match their prey's body size and locomotive abilities and therefore increase predation risk uniformly over both foraging sites and refuge sites that can both be entered by the predator. This reduces the costs of missing opportunities other than foraging. Voles changed their foraging strategy accordingly by specializing on the experimental food patches with predictable returns and probably reduced their foraging in the matrix of natural food source with unpredictable returns and high risk to encounter the weasel. Moreover, after 1 day of weasel presence, voles shifted their main foraging activities to avoid the diurnal weasel. This behavior facilitated bird predation, probably by nocturnal owls, and more voles were killed by birds than by weasels. Food patch use of voles in weasel enclosures increased with time. Voles had to balance the previously missed feeding opportunities by progressively concentrating on artificial food patches.

Polyphasic activity patterns in small mammals.

Cathemeral species are routinely active during the day, the night and at twilight. For the majority of species it is advantageous to specialize on the environmental conditions of a particular phase of the 24-hour day, so this rather uncommon type of activity must be a consequence of specific constraints. Good examples are the polyphasic activity patterns found in some small mammals. In shrews, with small body size and extremely high metabolic rate, polyphasic activity represents a simple short-term hunger cycle. In voles the short-term rhythm is triggered by an additional endogenous ultradian clock that interacts with the common circadian system, which probably is functionally related to endosymbiont digestion of cellulose-rich food. The activity bouts of individuals are synchronized on the population level to spread predation risk. As cathemeral species, voles are not specifically adapted to particular light conditions, but they are also not restricted to a particular activity phase. Therefore, the benefits from flexible responses in activity timing to environmental challenges may compensate for the disadvantages of not being specialized.

Breeding suppression in free-ranging grey-sided voles under the influence of predator odour.

The breeding suppression hypothesis predicts that females of certain small mammal species will reduce reproduction as a response to the odour of a specialised mammalian predator. This was tested in a field experiment with grey-sided voles (Clethrionomys rufocanus) during three summer seasons (1997-1999) in the subalpine tundra of northern Norway, which is a natural habitat of this species. In a first phase free-ranging voles in six unfenced 1-ha plots were monitored by live-trapping from June to August each year. In a second phase from August to September, three of the plots were sprayed with weasel (Mustela nivalis) odour to simulate increased apparent predation risk, while the remaining three plots served as untreated controls. On all plots voles were individually marked with ear tattoos and were regularly live-trapped during the whole breeding season to follow their performance. On the treatment plots the recruitment rate of juveniles did not increase in late summer as it did on the control plots. The proportion of reproductively non-active adult females was significantly higher on the treatment plots for both old and young females. Our results thus verify the breeding suppression hypothesis for the first time under natural conditions. However, the response in overwintered females is in conflict with the original hypothesis because the assumed fitness benefits from breeding delayed until the next season are inaccessible to them. As an alternative explanation we propose a short-term response of reduced activity and interrupted breeding until the predator has exploited and left the feeding patch. Such a "duck and cover" strategy would increase the fitness of females of all age classes when prey habitats are patchy.