Ornis Fennica 100: 170–187. 2023 Most studies on intraspecific competition, i.e., competition among individuals of the same species, have been conducted during the breeding season. Yet, at northern latitudes, intraspecific competition is expected to be particularly strong under the harsh weather conditions of the non-breeding season with limited number of resources available per individual. We studied the food-hoarding behaviour of wintering Eurasian Pygmy Owls (Glaucidium passerinum) along with sex- and age-specific spatial distribution in relation to fluctuating main prey abundance (voles) and conspecific density using a 15-year dataset. In low vole abundance years, increasing conspecific density reduced the total prey number stored by an owl, suggesting high costs of exploitative competition. The distance between the stores of nearest neighbours was greater when both were females, suggesting that the spatial avoidance is driven by sex-specific competition. However, food stores of females had a larger amount of prey items, especially when the nearest neighbour was of the same sex. The number of stores hoarded by an owl increased with increasing conspecific densities. Distributing the prey items to multiple store- sites instead of one (shifting from larder-hoarding towards scatter-hoarding) can help to reduce the overall loss to potential pilfering when conspecific density is high. These results combined suggest that high conspecific density inflames sex-specific interference competition, rather than solely exploitative competition, and in turn drives the observed sex-specific spatial distribution. Adopting a sex-specific spatial distribution according to hoarding and aggressive behaviour can be a way to reduce the severity of intraspecific competition locally and could have cascading effects on the prey community. E. Koivisto, G. Masoero, C. Morosinotto, E. Korpimäki, Section of Ecology, Department of Biology, FI-20014 University of Turku, Finland G. Masoero, Department of Biology, University of Ottawa, 30 Marie Curie, Ottawa, Canada & Swiss Ornithological Institute, Seerose 1, 6204 Sempach, Switzerland C. Morosinotto, Department of Biology, University of Padova, Via U. Bassi 58/B, 35131 Padova, Italy & National Biodiversity Future Center (NBFC), Piazza Marina 61, 90133 Palermo, Italy E. Le Tortorec, Department of Biological and Environmental Sciences, University of Jyväskylä, PO Box 35, FI‐40014 University of Jyväskylä, Finland * Corresponding author’s e-mail: elanko@utu.fi † These authors contributed equally Received 15 August 2023, accepted 19 January 2024 Conspecific density drives sex-specific spatial wintertime distribution and hoarding behaviour of an avian predator Elina Koivisto*†, Giulia Masoero†, Chiara Morosinotto, Eric Le Tortorec & Erkki Korpimäki 171 ORNIS FENNICA Vol.100, 2023 1. Introduction Competition, together with food abundance and predation risk, is one of the central drivers of animal behaviour, spatial distribution, and popu- lation dynamics (Sih et al. 1985, Gurevitch et al. 2000). High densities of competitors may lead to demographic or individual density-dependent effects, i.e., causing a decrease in fitness compo- nents such as survival (Armstrong et al. 2002) or fecundity (Korpimäki 1987, Ferrer & Donazar 1996, Both 1998). Competition occurs among in- dividuals exploiting the same resources belonging either to the same or different species (intraspe- cific or interspecific competition, respectively). Individuals within a species usually occupy highly similar niches, and thus competition is expected to be intense (Schoener 1974). Intraspecific competition is consequently often found to have a higher impact on fitness than interspecific com- petition (Carrete et al. 2006, Svanbäck et al. 2008, Morosinotto et al. 2017a). When resources become a limiting factor, either due to a decrease in their availability or to a higher number of competing individuals, intraspecific competition gets more intense and may affect reproductive success (Morosinotto et al. 2017a), food consumption and somatic growth rate (Amundsen et al. 2007). In general, compe- tition may involve indirect interactions through resource depletion, where some individuals are more effective at exploiting a certain resource, reducing the amount available to others (exploit- ative competition; Miller 1967, Charnov et al. 1976, Schoener 1983, review in Dhondt 2012). It may also involve direct interactions, such as fighting, theft or ritualised combat, where some individuals aggressively interfere with the use of resources by other competitors (interference competition; Miller 1967, Schoener 1983, review in Dhondt 2012). Negative effects of competition may further arise via resource depression (sensu Charnov et al. 1976), a process that does not require the actual capture of any prey by the predator. The presence of a predator may in fact bring about a decrease in the capture rate of the prey in its vicinity, due to the detrimental effects of its foraging activity on the behaviour and micro-distribution of prey. As competition is costly (e.g., Abramsky et al. 2001, review in Dhondt 2012), animals have evolved ways to reduce the costs of competition and to minimize the risk of aggressive interactions (e.g., Valeix et al. 2007, review in Dhondt 2012). Among these strategies, there is the selection of the habitat or territory where to live, trying to avoid areas with a high density of competitors (Avgar et al. 2020) or with scarce resources, and the niche separation between age classes or sexes (e.g., Svanbäck & Bolnick 2007). The difference in competitive abilities among individuals can affect their spatial distribution (ideal despotic dis- tribution; Fretwell 1972), where highly territorial dominant individuals will first occupy the best unoccupied sites (ideal pre-emptive distribution; Pulliam & Danielson 1991), while inferior competitors will have to settle for less favourable habitats (e.g., Ziv et al. 1993, Calsbeek & Sinervo 2002). Niche separation can rise from difference between age and sex classes in their respective competitive ability, as they often exhibit differ- ences in foraging due to experience, skills, or life history strategy (Marchetti & Price 1989, Smith & Metcalfe 1994, Coulson et al. 2001, Ishikawa & Watanuki 2002, Field et al. 2007, Faegre et al. 2020, Masoero et al. 2020). This marked differ- ence in experience and size leads to separation in prey selection. For example, many birds of prey show pronounced reversed sex-specific size dimorphism (i.e., females are the larger sex; Massemin et al. 2000, Krüger 2005, Korpimäki & Hakkarainen 2012). Larger females are capable of hunting for larger-sized prey, whereas smaller males can be more efficient hunters in catching agile prey, like birds (Mills et al. 2019), especially in structurally complex environments such as forests (Hakkarainen & Korpimäki 1991, Pérez- Camacho et al. 2015, 2018). A vast majority of studies on intraspecific com- petition in birds have been conducted during the breeding season, as direct effects on reproductive success are often of primary interest (e.g., Dann & Norman 2006, Denac 2006, Garabedian et al. 2022). Yet, at northern latitudes, intraspecific com- petition is expected to be particularly strong under the harsh climatic conditions of the non-breeding season, which can lead to food limitation, sig- nificant source of mortality during wintertime (Taylor 1994, Hakkarainen et al. 2002, Reigert & Fuchs 2011), and to skewing of the adult sex ratio Koivisto et al.: Density drives sex-specific spatial distribution and hoarding in Pygmy Owls 172 by sex-biased mortality (Chang & Wiebe 2016). Here, we investigate the wintertime sex- and age-specific spatial distribution of a small avian predator, the Eurasian Pygmy Owl (Glaucidium passerinum; hereafter “Pygmy Owl”), and its impact on the food hoarding of individuals (terms “storing” and “caching” are also used hereafter) using 15 years of data on food-store composition and captured individuals collected in Finland. The main prey of Pygmy Owls are voles of the genera Myodes and Microtus (Kellomäki 1977, Halonen et al. 2007, Masoero et al. 2020), which in North Europe exhibit three-year high-amplitude pop- ulation cycles (Korpimäki et al. 2005), resulting in pronounced among-year fluctuations in the abundance of main food for Pygmy Owls. During the breeding season, Pygmy Owls were found to avoid breeding close to conspecifics, but this avoidance decreased when voles were abundant (Morosinotto et al. 2017a). In autumn and early winter, Pygmy Owls store prey in natural cavities and nest boxes (Solheim 1984a, Terraube et al. 2017, Masoero et al. 2018, 2020). This behaviour has probably evolved to reduce starva- tion risk during winter, when resources are scarce (Vander Wall 1990). Like many species of birds of prey, also Pygmy Owls present reversed sexual size dimorphism, with females being larger than males, and show both age- and sex-specific differences in prey use (Masoero et al. 2018, 2020). When comparing the food-storing behaviour between the sexes and age classes, females and yearlings hoarded stores with a greater number of prey items than males and adults respectively (Masoero et al. 2018), stored more small mammals and tended to store fewer birds under low food availability (Masoero et al. 2020). Based on the previous knowledge on the density-dependent effects during the breeding season as well as the age- and sex-specific differences in hoarding behaviour, we expected that: 1) spatial distribution of Pygmy Owls will depend on age- and sex-specific hoarding strategies, as avoiding neighbours with similar hunting strategies reduces exploitative intraspe- cific competition, 2) owls will have more stores when conspecific density is high to decentralize stored prey items to avoid potential pilfering and interference competition, and 3) overall, high conspecific density, as well as the age and sex spatial distribution, will modify hoarding success (number of stored prey), especially when voles are scarce. 2. Material and methods 2.1. The study system The study area consists of ca. 1,000 km2 of forests and agricultural lands in the Kauhava region, western Finland (63°N, 23°E), where ca. 300 sites with two nest boxes per forest site were provided for Pygmy Owls (a landscape map of the study area with nest-box sites in Fig. S1 of Morosinotto et al. 2017a). The proportion of coniferous forests is 66% and that of agricultural land 25% of the study area. The management of the forest lands has created a mosaic of clear-cut and sapling areas as well as different-aged forests where the main tree species are scots pine (Pinus sylvestris), Norway spruce (Picea abies) and in smaller proportions some deciduous trees (Hakkarainen et al. 2003, Morosinotto et al. 2017a, Korpimäki et al. 2020). For more details on the habitat structure and vegetation age classes please see Morosinotto et al. (2017a) and Baroni et al. (2021). The data for this study were collected from 2003 to 2017. Pygmy Owls inhabit mature and old conif- erous forests of Europe and Asia (Schönn 1980, Strøm & Sonerud 2001, Barbaro et al. 2016, Morosinotto et al. 2017a). Natural tree cavities or artificial nest boxes are used in spring for breeding and late autumn and winter for storing food (Solheim 1984a, 1984b, Morosinotto et al. 2017a, Terraube et al. 2017). In autumn, all the box-sites were inspected twice (once in late October to early November and once in late November to early December) to collect data on the food stores and on the Pygmy Owl individuals storing the food items (for further details on the study system, see Terraube et al. 2017, Masoero et al. 2018). The total number of fresh prey items in the two autumn visits was calculated and, to avoid double-counting, prey items in food stores were marked with tail-clipping (mammals) or toe-clipping (birds). From 2003 to 2017, we collected data for a total of 1018 food stores, of which 643 had an identified food hoarder. On average, the annual 173 ORNIS FENNICA Vol.100, 2023 percentage (mean ± SD) of food stores with an identified hoarder was 63.2 ± 12.7%. Most owls (82%) at food stores were captured with nest-box traps (a replica of the box equipped with swing door) or with a telescopic fishing pole with a noose at the top, a capture commonly used with larger owl species (e.g., Forsman 1983, Bull 1990) and therefore safe for Pygmy Owls. Captured owls were ringed with an aluminium leg ring for individual identification, weighed, sexed, and aged, and wing and tail lengths were measured. The rest of the identities of hoarders (18%) were obtained using Passive Integrated Transponder (PIT) tags, a small electromagnetic microchip implanted subcutaneously when capturing the owls (Masoero et al. 2018). Data on encounters of individual owls were collected by placing the antenna of the reader around the entrance hole of the food-store box. The antenna and reader were set up when the food store was found but capturing the owl with the nest box trap failed. The antenna was then kept in place at least for two weeks or until the reader recorded the identity. As females are larger than males, sex was determined based on wing length, tail length, and body mass (as in Masoero et al. 2018). The age was estimated according to wing moult (Lagerström & Syrjänen 1990), and individuals were divided into two classes: individuals at their hatching year (1y = yearlings) and older individ- uals (Ad = adults). The abundance of the main prey (bank voles Myodes glareolus and Microtus voles, the fieldvole M. agrestis and the sibling vole M. rossiaemeridionalis; Kellomäki 1977, Halonen et al. 2007, Masoero et al. 2020) was estimated by snap trapping twice a year (early May and mid-September). In two locations 14 km apart within the study area, 50–60 metal mouse snap- traps were set up to cover 0.5 to 0.6 ha and the four main habitat types; agricultural and abandoned fields, and forests dominated by spruce or pine (Korpimäki et al. 2005). Live trapping was not feasible due to methodological constraints (see also Ethical approval section). The traps (baited with mixed-grain bread) were placed in vole runways and checked daily for three days. The regional synchrony of vole population cycles and thus indices of small mammals extend up to 80 km (Huitu et al. 2003, Korpimäki et al. 2005), therefore the validity of this index could be extended to the whole study area. The abundance of vole species in the study area fluctuates in three-year cycles with a 100-200-fold amplitude (see Korpimäki et al. 2005 for more details). To obtain an autumn vole abundance index for the analyses, the results from the three-night trapping sessions done in September for both the bank voles and Microtus voles (voles only) were pooled and standardised as the number of animals captured per 100 trap nights. For the analysis the continuous vole abundance data was changed into a categorical variable. To consider the actual abundance of main food resources in the current autumn, the variable was divided into three levels: “low” (0.1–3.0 animals captured per 100 trap nights), “intermediate” (3.1–12.0) and “high” (>12.0) abundance (Fig. 1a). 2.2. Owl density Pygmy Owl density was calculated at a 6000 m radius around a single food store of a focal Pygmy Owl. If the individual had more than one food store, a convex hull, which formed the smallest area that included the buffers around the individ- ual food stores and the area between them, was created. This convex hull reflected the area that an owl individual would have to fly across to move between nest-box sites. The results on a previous study on the same population shows that ca. three- fourths (299 owls out of 412) of the owls had only one store per storing season, whereas the rest had two to six food stores (Masoero et al. 2018). The value of 6000 m was chosen based on previous research since the home range size was estimated to be around 2.3 km2 (range 0.4–6.0 km2; Strøm & Sonerud 2001). The average distance between two stores of the same individual is known to be 1.5 km and the maximum distance is 5.0 km (Masoero et al. 2018). Thus, the chosen 6000 m radius is likely to include all the food stores of an individual. The density values were computed using the function ‘density’ in the package spatstat (R package v. 1.59-0; Baddeley et al. 2015), which computes a kernel smoothed intensity function from a pattern of points. Mean density values within buffers and convex hulls were extracted using the function ‘extract’ in the package raster Koivisto et al.: Density drives sex-specific spatial distribution and hoarding in Pygmy Owls 174 (R package v. 2.5-8; Hijmans & van Etten 2012). The distance between an individual and its nearest neighbour during a particular year was calculated from the coordinates of the boxes using the function ‘gDistance’ in the package GIStools (R package v. 0.7-4; Brunsdon & Chen 2014). 2.3. Statistical analyses To be able to detect whether distances between in- dividuals depend on sex, age, and food abundance, we need to estimate the proportional deviance between observed and randomly simulated values and then build a Linear Mixed-effects Model (LMM). Observed values were then compared to randomly distributed owls. Given the owls present each year, we generated 10,000 simulated datasets by re-assigning the owls to different food-hoard- ing boxes and then checking the identity of the new nearest neighbour (NN) and its distance from the focal owl. Using the average of the simulated values for the NN distance (simulated distance), we calculated the proportional deviance of the observed values as (obs–sim)/sim. Using an LMM, we then investigated whether the proportional deviance of the distance between an owl and its NN was related to the vole abundance level (three levels: “low”, “intermediate”, “high”), to the ages (“1y–Ad”, “1y–1y”, “Ad–Ad”), and sexes (“F–M”, “F–F”, “M–M”) of the two neighbours. Year was used as a random factor to control for environmental conditions in a certain year. We then tested the effects of competition on the number of food stores hoarded by an indi- vidual and the number of prey items stored (as proxies for hoarding success) using Generalised Linear Mixed-effects Models (GLMMs) with a Poisson family. As independent variables in both models, we considered the neighbouring owls’ density (continuous variable), and the categorical variables: vole abundance level, age (“1y” or “Ad”) and sex (“F” or “M”) of the hoarding owl and of its NN (to understand how characteristics of the NN can affect the hoarder). Continuous variables were standardised (µ=0 and σ2=1) using the scale function in R. The identity of the owl and year were used as random factors in the GLMMs to control for multiple stores from the same individual and for environmental conditions in a certain year. We used the dredge function within the package MuMIn (Bartoń 2023) to apply model selection (model selection tables for the number of food stores hoarded by an individual and the number of prey items stored can be found in Supplementary materials S1 and S2, respectively). The optimal model was selected using Akaike Information Criterion corrected for small sample size (AICc) values. If the difference between the model with the lowest AICc and the second one was smaller than two, we decided to keep the most parsimonious model. We fixed vole index, age, and sex of the hoarder to be kept in all models since their significance for the food-hoarding Pygmy Owls is already known (Masoero et al. 2018). The three two-way interactions between neighbour density and vole abundance level, age of the hoarder and age of the NN and between sex of the hoarder and sex of its NN were also tested. All analyses were carried out using R v. 4.1.0 (R Core Team 2022), and all GLMMs were run using the package lme4 (Bates et al. 2015). 3. Results 3.1. Conspecific density Variations in both the number of food-hoarding owls and in the conspecific density generally followed variation in vole abundance (Fig. 1). The number of food-hoarding owls varied from a minimum of 13 (2006) to a maximum of 60 (2011) during the 15 years of the study (Fig 1b) in the study area. Conspecific density in the 6000 m radius around the food stores of a focal indi- vidual was on average (± SD) 0.05 (± 0.03) and ranged between 0.002–0.150, varying among years (Fig 1c). 3.2. Distance to nearest neighbour Concerning the spatial distribution of Pygmy Owls, we found that the proportional deviance between observed distance of food stores of NNs from the random distances (calculated as (obs– sim)/sim) was significantly different according to the sexes of the two NNs. In particular, the 175 ORNIS FENNICA Vol.100, 2023 distance between stores of neighbouring owls was similar to what simulated by random (values of proportional deviance ∼ 0) if the two owls were both females (Fig. 2; mean linear distance ± SD: 3.6 ± 2.3 km), whereas stores between male neighbours (2.8 ± 1.8 km) and different sex neigh- bours (2.7 ± 1.8 km) were closer than simulated by random (proportional deviance < 0) (Table 1, Fig. 2). 3.3. Number of stores per individual The top model for the number of stores per individual included only a significant effect of conspecific density (see Supplementary materials Table S1 for the model selection table). This means that the number of food stores hoarded by a focal individual increased with increasing density of surrounding Pygmy Owls (Table 2, Fig. 3), but was not affected by level of vole abundance, age, or sex of the hoarding individual. 3.4. Hoarding success The top model for the total number of prey items stored by an owl (hoarding success) included all the variables and two of the tested two-way in- teractions (Table 3; see Supplementary materials Table S2). The interaction between conspecific density and level of vole abundance (Fig. 4a) Fig. 1. Among-year variation in (a) autumn vole abundance (number of individuals captured per 100 trap nights), (b) number of food-hoard- ing individuals and (c) mean (and standard deviation) conspecific den- sity in the 6000 m radius around the food stores of a focal individual in the study area during 2003–2017. In panel (a), the colours represent the subdivision of the vole abundance in 3 levels: low (0–3) in yellow, interme- diate (3–12) in green, and high (>12) in purple. Colour figure is available in the online version of the article at https://doi.org/10.51812/of.130326. Koivisto et al.: Density drives sex-specific spatial distribution and hoarding in Pygmy Owls 176 indicates that when vole abundance is low, the in- creasing density of conspecifics is associated with a decreasing amount of food stored. In intermedi- ate and high years of vole abundance, increasing density of conspecifics is associated with, respec- tively, either no relationship or increased number of food items stored (Table 3). The interaction between the age of the hoarder and the age of its NN was not significant and was not present in the best model. Yearlings showed a tendency to store more prey items than adults (Fig. 4b), and owls with a yearling NN stored more prey items that owls with an adult NN (Fig. 4c). The interaction between the sex of the hoarder and the sex of the NN indicates that there were some significant dif- ferences between groups (Fig. 4d) that were tested using post-hoc Tukey tests. Female hoarders with a female NN hoarded more prey than females with a male NN (z = –7.20, p<0.0001), or male hoarders independently of the sex of their NN (with female NN: z = –4.60, p<0.0001; with male NN: z = 5.27, p<0.0001). Fig. 2. Predicted values (and 95% CI) of the proportional deviance for the distance between nearest neighbours (NN) in relation to the sexes of the NNs (see Table 1). Observed values are represented with jittered semi-transparent dots, with darker colours meaning a higher number of observations. The histograms on top of the panel represent the dis- tribution of the actual distances between NNs in km (light grey bars), with the mean value for each group represented with a dark grey vertical line. N=295 NNs. 177 ORNIS FENNICA Vol.100, 2023 4. Discussion We expected Pygmy Owls to avoid neighbours with similar hunting strategies (same sex or same age) to reduce exploitative intraspecific competition. In accordance with this expectation, the observed distance between stores of nearest neighbours was larger when the neighbours were both females. According to proportional deviance, male-male and male-female pairs seemed to be closer to each other than expected by random. Despite this spatial distribution, food stores were mostly larger when the hoarder was a female and especially so when the nearest neighbour was also female. In contrast, we found no age-specific spatial distribution but having yearlings as neigh- bours led to overall higher hoarding success, suggesting a benefit from having neighbours with modest hunting experience. The number of prey items stored by an owl depended on vole abundance as well as conspecific density, suggesting high costs of exploitative competition when food is scarce. However, in high years of vole abundance, increasing conspecific density resulted in a larger number of stored prey items, probably indicating an overall positive effect of food abundance on population densities. As expected, the number of stores hoarded by an owl increased with increasing conspecific densities to decentralize stored prey items to avoid potential Explanatory Estimate ± SE Chisq p Intercept 0.100 ± 0.106 Vole abundance 1.05 0.5903 Low 0 ± 0 Intermediate 0.056 ± 0.095 High –0.018 ± 0.103 NNs - ages 0.29 0.8658 Ad – Ad 0 ± 0 1y – Ad –0.003 ± 0.086 1y – 1y 0.079 ± 0.093 NNs - sexes 10.64 0.0049 F – F 0 ± 0 M – F –0.260 ± 0.082 M – M –0.249 ± 0.101 Table 1. LMMs analysing the proportional deviation from random distances between the food stores of two nearest neighbours (NN) according to the lev- el of vole abundance, age, and sex of the NNs. All models included ‘year’ as a random factor. Signifi- cant variables (p<0.05) are shown in bold. N=295 NNs. Explanatory Estimate ± SE Chisq p Intercept 0.471 ± 0.119 Conspecific density 0.181 ± 0.048 14.09 0.0002 Vole abundance Low 0 ± 0 1.43 0.4883 Intermediate –0.091 ± 0.124 High –0.181 ± 0.152 Hoarder age Ad 0 ± 0 0.07 0.7894 1y 0.022 ± 0.084 Hoarder sex F 0 ± 0 0 0.9999 M 0 ± 0.081 Table 2. GLMMs on the to- tal number of food stores per individual in relation to conspecific density at 6000 m. Explanatory var- iables also included vole abundance level (Low, Intermediate, High), age (1y = yearlings and Ad = Adults) and sex (M = males and F = females) of the hoarder. All mod- els included year and individual identity of the owl as random factors. Significant variables (p< 0.05) are shown in bold. N=428 cases for 327 indi- viduals in 15 years. Koivisto et al.: Density drives sex-specific spatial distribution and hoarding in Pygmy Owls 178 Fig. 3. Predicted values (and 95% CI) of the total number of food stores per individual in re- lation to conspecific density in a 6000 m radius based on the models in Table 2. Observed values are represented with semi-transparent dots, with darker colours meaning a high- er number of observations. Table 3. GLMMs analysing the variation in hoarding success (as total number of prey items stored by one individual) in relation to conspecific density in a 6000 m radius from its store(s), vole abundance level (Low, Intermediate, High), age (1y = yearlings and Ad = adults) and sex (M = males and F = females) of the hoarder and of the nearest neighbour (NN). The symbol “X” denotes an interaction. All models included year and owl identity as random factors. Significant variables (p<0.05) are shown in bold. N=428 cases for 327 individuals in 15 years. Explanatory Estimate ± SE Chisq p Intercept 1.694 ± 0.246 Conspecific density X Vole abundance Low 0 ± 0 53.22 <0.0001 Intermediate 1.101 ± 0.168 High 1.225 ± 0.169 Conspecific density –1.041 ± 0.178 14.64 0.0001 Vole abundance Low 0 ± 0 5.69 0.0581 Intermediate 1.443 ± 0.272 High 1.593 ± 0.334 Hoarder age 1yr 0.084 ± 0.045 3.52 0.0605 Ad 0 ± 0 NN age 1y 0.237 ± 0.050 22.16 <0.0001 Ad 0 ± 0 Hoarder sex X NN sex M–M 0.430 ± 0.093 21.35 <0.0001 others 0 ± 0 Hoarder sex M –0.526 ± 0.114 8.81 0.0030 F 0 ± 0 NN sex M –0.521 ± 0.072 33.05 <0.0001 F 0 ± 0 179 ORNIS FENNICA Vol.100, 2023 pilfering and interference competition. These results suggest that high conspecific density overall inflames interference competition when food availability is low and leads to sex-specific spatial distribution. 4.1. Sex-specific competition Pygmy Owls showed sex-specific spatial distri- bution. Females had overall larger distances to same-sex neighbours compared to male-male neighbours or neighbours of the opposite sex, which were instead closer to each other than expected at random. Close distances between the stores of male-male and opposite-sex neighbours were associated which led to higher conspecific density, but their different hoarding strategies and diverse diet could reduce the costs of exploitative competition. Males can hunt a large array of prey including small birds along with small mammals while females mostly hunt voles (Masoero et al. 2020). Therefore, the intrasexual exploitative competition among males, or between sexes, may be reduced since individuals may specialize on different prey groups. Interference competition and especially conspecific aggression could also be reduced if the neighbours are of opposite sex, or both are males. Female Pygmy Owls are larger and likely need more food than males and indeed store larger food hoards (Masoero et al. 2018). The energy requirement of an individual increases Fig. 4. Predicted values (and 95% CI) of total number of prey items stored (hoarding success) in all the food stores of one individual Pygmy Owl in relation to (a) the conspecific density in a 6000 m radius, (b) age of the hoarder, (c) of its NN, and (d) the interaction sex of the hoarder and of its NN. Predicted values are based on the models in Table 3. In plot (a), the three lines represent the different levels of vole abundance: low in yellow, intermediate in green, high in purple. Observed values are represented with dots, with darker colours meaning a higher number of observations. Colour figure is available in the online version of the article at https://doi.org/10.51812/of.130326. Koivisto et al.: Density drives sex-specific spatial distribution and hoarding in Pygmy Owls 180 together with body size (Schmidt-Nielsen & Knut 1984), and therefore leads to a consequent increase in space used (Jetz et al. 2004). Indeed, females are known to be more aggressive toward conspecifics at least during the breeding season (Mikusek 2019). During the hoarding season their aggressive behaviour could lead females to occupy wider territories, and thus to have stores further away from each other. These results suggest that there is an asymmetry in the compet- itive abilities of males and females. This supports previous studies which show that individuals of the larger sex (females in our case) exert stronger competition by acquiring resources at the expense of others (Oddie 2000, Bedhomme et al. 2003), and they can respond more strongly than males to the presence of a competing female (Iglesias- Carrasco et al. 2020). The sex-specific spatial distribution that we observed here is thus probably a combined result of exploitative and interference competition. The role of interference competition is suggested by the fact that the hoarding success of female owls with a same-sex neighbour was higher than owls with different-sex neighbours or male owls. The larger territories of females with same-sex neigh- bours, being in average 1 km further apart from their neighbours compared to individuals with opposite-sex neighbours or male-male neighbours (see results), probably derive from the high intrasexual aggression. These large territories could be beneficial not only to reduce interference competition but also as they reduce exploitative competition due to higher prey availability. On the other hand, being closer than expected to a neighbour with different hoarding strategy could also be beneficial in terms of reduced interference competition, while the diverse diet can help to reduce the costs of living at closer distance and thus alleviate exploitative competition. Different individuals thus seem to adopt different strategies to cope with the cost of aggressive interactions (interference competition) and the cost of exploit- ative completion at high densities, thus resulting in a sex-specific spatial distribution of stores. Overall, our findings indicate that Pygmy Owls show sex-specific responses to competitor sex, supporting previous studies showing that under resource limitation, the larger sex is at a disadvan- tage due to the costs of producing and maintaining a large body (Wikelski & Thom 2000, Benito & González‐Solís 2007). Our results also confirm the importance of considering not only the age and sex characteristics of the focal owl but also of their competitors when evaluating competition (Bonisoli-Alquati et al. 2011, Iglesias-Carrasco et al. 2020). We also suggest that Pygmy Owls might avoid same-sex nearest neighbours to further release the intrasexual interference competition and resource depression (sensu Charnov et al. 1976). In general, interference competition can be exhausting by reducing food availability and the energy allocated in competition is then unavailable for other functions (Jaeger et al. 1983, Cresswell 1997), which in turn can lead to reduced fitness (Eccard & Ylönen 2002). Therefore, intraspecific competition and resource depression are probably among the main drivers in regulating wintering population of Pygmy Owls, as suggested for other predators (e.g., Cubaynes et al. 2014), and behav- ioural mechanisms releasing this competition can thus be highly beneficial. In addition, interspecific competition with other predators subsisting small mammals may also be important, because Pygmy Owls are able to store less food in the presence of larger Tengmalm’s Owls (Aegolius funereus; Suhonen et al. 2007). 4.2. Conspecific density and resource abundance The number of stores hoarded by an owl increased with increasing conspecific densities. Allocating prey in several food stores can reduce transportation distance and, thus, energetic costs. Distributing prey items to multiple store-sites instead of one (shifting from larder-hoarding towards scatter-hoarding) can help to reduce the overall loss to potential pilfering when the con- specific density is high (Vander Wall & Jenkins 2003). Pygmy Owls can visit each other’s food stores (Masoero et al. 2018) and multiple food stores likely reduce pilfering from conspecifics or other small predators, such as small mustelids (Mustela sp.), which also increase in numbers during years of vole abundance (Korpimäki et al. 1991). When food is abundant, the variance in competitive abilities might be higher, because also more inexperienced or inferior competitors may be able to survive in the population and be 181 ORNIS FENNICA Vol.100, 2023 more prone to conduct pilfering, as shown in other food-hoarding species (e.g., American red squirrels Tamiasciurus hudsonicus; Donald & Boutin 2011). A high density of competitors will increase both exploitative and interference com- petition and having several hunting grounds might dilute this effect. It has been found that animals can adjust their behavioural patterns according to the assessed population density (Dantzer et al. 2012), so it can be suggested that showing activity in multiple store locations could also be a way for Pygmy Owls to strengthen their territory ownership, which can, in turn, reduce the confron- tations from intruders. In low vole abundance years, conspecific density decreased the total prey number stored by an owl, showing high costs of competition. This is in line with previous studies showing that when resources are scarce, intraspecific exploitative competition is stronger (e.g., Amundsen 2007, Morosinotto et al. 2017a). Hoarding success increased with conspecific density in high vole years in early winter, which is consistent with an earlier finding that Pygmy Owls avoided breeding close to each other but less so when food was plentiful (Morosinotto et al. 2017a). When voles are abundant, also the number of Pygmy Owls over-wintering in the area is high (Masoero et al. 2020) but, due to the good food availability, the intraspecific competition per se appeared to be relaxed. This shows the crucial role of the high-amplitude vole cycles for the predator community in northern areas. Voles are keystone herbivores in boreal landscapes and the main food source for a whole predator community, consisting of several avian and mammalian predators (e.g., Korpimäki 1987, Korpimäki et al. 1991). Accordingly, Dhondt (2012) highlights the importance of resource availability for intraspecific competition. It is often difficult to disentangle the effects of food availability and population density when they are highly intertwined (Dantzer et al. 2012). For example, and consistently with our results, in breeding Eagle Owls (Bubo bubo) the popu- lation growth rate is positive in low conspecific abundance, whereas it tends to be negative when conspecific abundance is high (Fernandez-de- Simon et al. 2014). Population growth was also positively related to the density of Eagle Owls’ main prey (rabbits Oryctolagus cuniculus), when considering Eagle Owl conspecific abundance (Fernandez-de-Simon et al. 2014). Especially in systems with drastically varying food supply from year to year, the focus of the competition can fluctuate between food (when food is scarce) and space, like roosting sites during winter, when food is not the limiting factor. 4.3. Age-specific effects Pygmy Owls did not seem to spatially avoid indi- viduals according to age, because the age of the nearest neighbour only slightly affected hoarding success. Hoarders with a yearling neighbour had larger food stores than hoarders with an adult neighbour, but independently from the hoarder’s age. Young competitors likely lack the same experience in hunting as adults have, as shown in numerous other species (Marchetti & Price 1989, Wunderle 1991), and they are usually at a disadvantage when having to compete with adult individuals (Donázar et al. 1999, Smallegange & van der Meer 2006, Breed at al. 2013). Among food-hoarding species as well, young individuals face a higher risk of pilfering than adult individ- uals due to their lower experience (Beck et al. 2020). Furthermore, adults appear to be able to hunt a wider variety of prey (Masoero et al. 2020) and therefore might suffer less from competition. As adult owls cache also more small birds, they could be more mobbed. Intra and interspecific collaborative mobbing/antipredator behaviours from prey (Bshary & NoË 1997, Templeton et al. 2005, Dutour et al. 2016) may interfere with the hunting of many predators in the same forest patch and induce depression of food resources (sensu Charnov et al. 1976). Individuals may therefore be favoured by competing with a young neighbour and avoid food depletion by an adult neighbour due to intense mobbing of small birds. 4.4. Concluding remarks Our results highlight the importance of intra- specific competition during a non-breeding season. We found that in food-hoarding predators high wintertime conspecific densities can lead Koivisto et al.: Density drives sex-specific spatial distribution and hoarding in Pygmy Owls 182 to a lowered food-storing success, which can, in turn, decline the chances for over-winter survival or reduce breeding success in the following year. Therefore, in harsh winter conditions, sex-specific spatial segregation in species with sex-depend- ent hunting differences could have evolved to reduce the costs of interference competition rather than exploitative competition. Having the right neighbour can help to reduce the severity of intraspecific competition locally, as sexes are known to have differences in diet and hunting behaviour (Mills et al. 2019, Masoero et al. 2020). When predators are in question, the outcome of their interactions will also indirectly impact prey populations (Ritchie & Johnson 2009), because prey will modify their habitat choice according to the spatial distribution of predators (Korpimäki et al. 1996, Morosinotto et al. 2010, Byholm et al. 2012). As male Pygmy Owls hunt more birds than females do, the sex-specific spatial settlement patterns of wintering Pygmy Owls can further modify the habitat selection of their main and alternative prey, voles, and small passerine birds, respectively. Since harsh winter months are critical for the abundance and condition of small birds in boreal forests (e.g., Morosinotto et al. 2017b), even small-scale habitat decisions made by predators can have severe consequences on a wintering animal. Thus, understanding how conspecific predators interact and how this can impact their spatial distribution and hunting success is crucial to investigate predator effects at a landscape scale. Lajinsisäinen tiheys ohjaa varpuspöllön suku- puolikohtaista alueellista talvilevittäytymistä ja ravinnonkeräämiskäyttäytymistä Useimmat tutkimukset lajinsisäisestä kil- pailusta on tehty pesimäkaudella. Pohjoisilla leveysasteilla lajinsisäisen kilpailun kuiten- kin odotetaan olevan erityisen voimakasta pesi- mäkauden ulkopuolella, kun sääolosuhteet ovat ankarat ja resursseja on tarjolla rajallisesti. Tässä tutkimuksessa tarkastelimme talvehtivien var- puspöllöjen (Glaucidium passerinum) ravin- nonkeräämiskäyttäytymistä 15 vuoden ajalta. Lisäksi analysoimme sekä sukupuoli- että ikä- kohtaista alueellista levittäytymistä suhteessa vaihtelevaan pääsaaliin (myyrien) runsauteen ja lajinsisäiseen tiheyteen. Huonoina myyrävuosina korkeampi lajinsi- säinen tiheys vähensi varpuspöllöjen varastoi- man saaliin kokonaismäärää, mikä voi johtua epäsuoran resurssikilpailun korkeista kustannuk- sista. Etäisyydet ruokavarastojen välillä olivat pidempiä silloin, kun lähimmät naapurit olivat naaraita, mikä viittaa alueellisen käyttäytymisen liittyvän sukupuolikohtaiseen kilpailuun. Naa- rasvarpuspöllöjen varastot sisälsivät kuitenkin enemmän saalista erityisesti silloin, kun lähin naapuri oli samaa sukupuolta. Yksilöt varastoi- vat enemmän saalista varpuspöllöpopulaation tiheyden kasvaessa. Saaliiden jakaminen useille varastopaikoille yhden sijasta voi auttaa vähen- tämään mahdollisia varkauksia pöllöpopulaation tiheyden ollessa suuri. Nämä tulokset yhdistettyinä viittaavat siihen, että suuri lajinsisäinen tiheys kärjistää suku- puolisidonnaista suoraa häirintäkilpailua (eikä pelkästään epäsuoraa resurssikilpailua), mikä puolestaan voi johtaa havaitsemaamme suku- puolikohtaiseen alueelliseen levittäytymiseen. Ravinnonkeräämis- ja häirintäkäyttäytymisen perusteella sukupuolikohtainen alueellinen levit- täytyminen voi olla keino vähentää lajinsisäisen kilpailun voimakkuutta paikallisesti. Sillä voi olla myös kerrannaisvaikutuksia saalisyhteisöön. Acknowledgements. We thank Jorma Nurmi, Rauno Varjonen, Kari Hongisto, Julien Terraube, Alexandre Villers, Brigitte Planade, Michel Griesser, Claire Cuginiere, Stefan Siivonen, Léo Poudré, Robert L. Thomson and Ville Vasko for great help with the fieldwork. Thanks to Andrea Santangeli for the statistical discussions. Competing interests and funding. The study was financially supported by the Academy of Finland (grant nos. 123379, 136717 and 250709 to EKor). EKoi was financially supported by the Finnish Cultural Foundation's South Ostrobothnia Regional Fund and GM by the University of Turku Graduate School (UTUGS). The authors declare no conflict of interest. Author contributions statement. EKoi, CM, GM and EKor conceived the ideas and designed meth- odology; EKor, GM and CM collected the data; 183 ORNIS FENNICA Vol.100, 2023 GM and ELT analysed the data; EKoi, GM and CM led the writing of the manuscript. All authors contributed critically to the drafts and gave final approval for publication. Data Availability Statement. The data (https://doi. org/10.17605/OSF.IO/ACWKS) is available at the following link: https://osf.io/acwks/. Please note that the location data are not included to avoid endangering the nesting sites of the Pygmy Owls. Ethical approval. Trapping and ringing of Pygmy Owls were executed under the ringing licence (no. 524 to EKor) by Ringing Centre of the Finnish Museum of the Natural History. Pit-tags were used in accordance with Finnish and EU Laws and regulations and under the approval of the Animal Experiment Committee of the State Provincial Office (Etelä-Suomen aluehallinto- virasto ESAVI; permit numbers: ESAVI-2010- 05480/Ym-23, ESAVI/3221/04.10.07/2013, ESAVI/3021/04.10.07/2017). Ethical approval from ethics committee for involving animals in this study was not required. All applicable inter- national, national and/or institutional guidelines for the use of animals were followed and all methodologies adopted in this manuscript were in line with Finnish law, including snap trapping of small rodents. References Abramsky, Z., Rosenzweig, M.L. & Subach, A. 2001: The cost of interspecific competition in two gerbil species. — Journal of Animal Ecology 70: 561–567. https://doi. org/10.1046/j.1365-2656.2001.00520.x Amundsen, P.-A., Knudsen, R. & Klemetsen, A. 2007: In- traspecific competition and density dependence of food consumption and growth in Arctic charr. — Journal of Animal Ecology 76: 149–158. https://doi.org/10.1111/ j.1365-2656.2006.01179.x Armstrong, D.P., Davidson, R.S., Dimond, W.J., Perrott, J.K., Castro, I., Ewen, J.G., Griffiths, R. & Taylor, J. 2002: Population dynamics of reintroduced forest birds on New Zealand islands. — Journal of Biogeography 29: 609–621. https://doi.org/10.1046/j.1365-2699. 2002.00710.x Avgar, T., Betini, G.S. & Fryxell, J.M. 2020: Habitat selec- tion patterns are density-dependent under the Ideal Free Distribution. — Journal of Animal Ecology 89: 2777– 2787. https://doi.org/10.1111/1365-2656.13352 Baddeley, A., Rubak, E. & Turner, R. 2015: Spatial Point Patterns: Methodology and Applications with R. — Chapman and Hall/CRC Press, London. http://www. crcpress.com/Spatial-Point-Patterns-Methodolo- gy-and-Applications-with-R/Baddeley-Rubak-Turn- er/9781482210200/ Barbaro, L., Blache, S., Trochard, G., Arlaud, C., de La- coste, N. & Kayser, Y. 2016: Hierarchical habitat selec- tion by Eurasian pygmy owls Glaucidium passerinum in old-growth forests of the southern French Prealps. — Journal of Ornithology 157: 333–342. https://doi. org/10.1007/s10336-015-1285-3 Baroni, D., Masoero, G., Korpimäki, E., Morosinotto, C. & Laaksonen, T. 2021: Habitat choice of a secondary cav- ity user indicates higher avoidance of disturbed habitat during breeding than during food-hoarding. — Forest Ecology and Management 483: 118925. https://doi. org/10.1016/j.foreco.2021.118925 Bartoń, K. 2023: MuMIn: Multi-Model Inference. R pack- age version 1.47.5. https://cran.hafro.is/web/packages/ MuMIn/MuMIn.pdf Bates, D., Maechler, M., Bolker, B. & Walker, S. 2015: Fit- ting Linear Mixed-Effects Models using lme4. R pack- age v. 1.1-15. — Journal of Statistical Software 67: 1–48. https://doi.org/10.18637/jss.v067.i01 Beck, K.B., Loretto, M.-C. & Bugnyar, T. 2020: Effects of site fidelity, group size and age on food-caching behav- iour of common ravens, Corvus corax. — Animal Be- havior 164: 51–64. https://doi.org/10.1016/j.anbe- hav.2020.03.015 Bedhomme, S., Agnew, P., Sidobre, C. & Michalakis, Y. 2003: Sex‐specific reaction norms to intraspecific lar- val competition in the mosquito Aedes aegypti. — Jour- nal of Evolutionary Biology 16: 721–730. https://doi. org/10.1046/j.1420-9101.2003.00576.x Benito, M.M. & González‐Solís, J. 2007: Sex ratio, sex‐ specific chick mortality and sexual size dimorphism in birds. — Journal of Evolutionary Biology 20: 1522– 1530. https://doi.org/10.1111/j.1420-9101.2007.01327.x Bonisoli‐Alquati, A., Boncoraglio, G., Caprioli, M. & Sai- no, N. 2011: Birth order, individual sex and sex of com- petitors determine the outcome of conflict among sib- lings over parental care. — Proceedings of the Royal Society B: Biological Sciences 278: 1273–1279. https://doi.org/https://doi.org/10.1098/rspb.2010.1741 Both, C. 1998: Experimental evidence for density depend- ence reproduction in great tits. — Journal of Animal Ecology 67: 667–674. https://www.jstor.org/sta- ble/2647286 Breed, G.A., Bowen, W.D. & Leonard, M.L. 2013: Behav- ioral signature of intraspecific competition and density dependence in colony‐breeding marine predators. — Ecology and Evolution 3: 3838–3854. https://doi. org/10.1002/ece3.754 Brunsdon, C. & Chen, H. 2014: GISTools: Some further GIS capabilities for R. http://CRAN.R-project.org/ Koivisto et al.: Density drives sex-specific spatial distribution and hoarding in Pygmy Owls 184 packageGISTools Bshary, R. & NoË, R. 1997: Red colobus and Diana mon- keys provide mutual protection against predators. — Animal Behaviour 54: 1461–1474. https://doi. org/10.1006/anbe.1997.0553 Bull, E.L. 1990: Ecology of the great gray owl. — US De- partment of Agriculture, Forest Service, Pacific North- west Research Station. https://doi.org/10.2737/PNW- GTR-265 Byholm, P., Burgas, D., Virtanen, T. & Valkama, J. 2012: Competitive exclusion within the predator community influences the distribution of a threatened prey species. — Ecology 93: 1802–1808. https://doi.org/10.1890/12- 0285.1 Calsbeek, R. & Sinervo, B. 2002: An experimental test of the ideal despotic distribution. — Journal of Animal Ecology 71: 513–523. https://doi.org/10.1046/ j.1365-2656.2002.00619.x Carrete, M., Sánchez-Zapata, J.A. & Tella, J.L. 2006: Com- ponents of breeding performance in two competing species: habitat heterogeneity, individual quality and density-dependence. — Oikos 112: 680–690. https:// doi.org/10.1111/j.0030-1299.2006.14528.x Chang, A.M. & Wiebe, K.L. 2016: Body condition in Snowy Owls wintering on the prairies is greater in fe- males and older individuals and may contribute to sex-biased mortality. — The Auk 133: 738–746. https:// doi.org/10.1642/AUK-16-60.1 Charnov, E.L., Orians, G.H. & Hyatt, K. 1976: Ecological implications of resource depression. — American Nat- uralist 110: 247–259. https://doi.org/10.1086/283062 Coulson, T., Catchpole, E.A., Albon, S.D., Morgan, B.J.T., Pemberton, J.M., Clutton-Brock, T.H., Crawley, M.J. & Grenfell, B.T. 2001: Age, Sex, Density, Winter Weather, and Population Crashes in Soay Sheep. — Science 292: 1528–1531. https://doi.org/10.1126/sci- ence.292.5521.1528 Cresswell, W. 1997: Interference Competition at Low Com- petitor Densities in Blackbirds Turdus merula. — Jour- nal of Animal Ecology 66: 461–471. https://doi. org/10.2307/5941 Cubaynes, S., MacNulty, D.R., Stahler, D.R., Quimby, K.A., Smith, D.W. & Coulson, T. 2014: Density‐de- pendent intraspecific aggression regulates survival in northern Yellowstone wolves (Canis lupus). — Journal of Animal Ecology 83: 1344–1356. https://doi. org/10.1111/1365-2656.12238 Dann, P. & Norman, F.I. 2006: Population regulation in Little Penguins (Eudyptula minor): the role of intraspe- cific competition for nesting sites and food during breeding. — Emu - Austral Ornithology 106: 289–296. https://doi.org/10.1071/MU06011 Dantzer, B., Boutin, S., Humphries, M.M. & McAdam, A.G. 2012: Behavioral responses of territorial red squirrels to natural and experimental variation in popu- lation density. — Behavioral Ecology and Sociobiolo- gy 66: 865–878. https://doi.org/10.1007/s00265-012- 1335-2 Denac, D. 2006: Intraspecific Exploitation Competition as Cause for Density Dependent Breeding Success in the White Stork. — Waterbirds 29: 391–394. https://doi.or g/10.1675/1524-4695(2006)29[391:IECACF]2.0. CO;2 Dhondt, A.A. 2012: Interspecific competition in birds. — Oxford University Press, Oxford. Donald, J.L. & Boutin, S. 2011: Intraspecific cache pilfer- age by larder-hoarding red squirrels (Tamiasciurus hudsonicus). — Journal of Mammalogy 92: 1013– 1020. https://doi.org/10.1644/10-MAMM-A-340.1 Donázar, J.A., Travaini, A., Ceballos, O., Rodríguez, A., Delipes, M. & Hiraldo, F. 1999: Effects of sex-associat- ed competitive asymmetries on foraging group struc- ture and despotic distribution in Andean condors. — Behavioral Ecology and Sociobiology 45: 55–65. https://doi.org/10.1007/s002650050539 Dutour, M., Lena, J.P. & Lengagne, T. 2016: Mobbing be- haviour varies according to predator dangerousness and occurrence. — Animal Behaviour 119: 119–124. https://doi.org/10.1016/j.anbehav.2016.06.024 Eccard, J.A. & Ylönen, H. 2002: Direct interference or indi- rect exploitation? An experimental study of fitness costs of interspecific competition in voles. — Oikos 99: 580–590. https://doi.org/10.1034/j.1600-0706.2002. 11833.x Faegre, S.K., Nietmann, L., Hannon, P., Ha, J.C. & Ha, R.R. 2020: Age‑related differences in diet and foraging be- havior of the critically endangered Mariana Crow (Cor- vus kubaryi), with notes on the predation of Coenobita hermit crabs. — Journal of Ornithology 161: 149–158. https://doi.org/10.1007/s10336-019-01705-3 Fernandez-de-Simon, J., Díaz-Ruiz, F., Cirilli, F., Tortosa, F.S., Villafuerte, R. & Ferreras, P. 2014: Role of prey and intraspecific density dependence on the population growth of an avian top predator. — Acta Oecologica 60: 1–6. https://doi.org/10.1016/j.actao.2014.06.006 Ferrer, M. & Donazar, J.A. 1996: Density-dependent fecun- dity by habitat heterogeneity in an increasing popula- tion of Spanish imperial eagles. — Ecology 77: 69–74. https://doi.org/10.2307/2265655 Field, I.C., Bradshaw, C.J.A., van den Hoff, J., Burton, H.R. & Hindell, M.A. 2007: Age-related shifts in the diet composition of southern elephant seals expand overall foraging niche. — Marine Biology 150: 1441–1452. https://doi.org/10.1007/s00227-006-0417-y Fretwell, S.D. 1972: Populations in a seasonal environment. — Princeton University Press, Princeton. Forsman, E.D. 1983: Methods and materials for locating and studying spotted owls. — US Department of Agri- culture, Forest Service, Pacific Northwest Forest and Range Experiment Station. https://doi.org/10.2737/ PNW-GTR-162 Garabedian, J.E., Moorman, C.E., Peterson, M.N. & Kilgo, J.C. 2022: Group size mediates effects of intraspecific competition and forest structure on productivity in a 185 ORNIS FENNICA Vol.100, 2023 recovering social woodpecker population. — Animal Conservation 25: 438–452. https://doi.org/10.1111/ acv.12757 Gurevitch, J., Morrison, J.A. & Hedges, L.V. 2000: The in- teraction between competition and predation: a me- ta-analysis of field experiments. — American Natural- ist 155: 435–453. https://doi.org/10.1086/303337 Hakkarainen, H. & Korpimäki, E. 1991: Reversed sexual size dimorphism in Tengmalm’s Owl: is small male size adaptive? — Oikos 61: 337–346. https://doi. org/10.2307/3545241 Hakkarainen, H., Korpimäki, E., Koivunen, V. & Ydenberg, R. 2002: Survival of male Tengmalm's owls under tem- porally varying food conditions. — Oecologia 131: 83–88. https://doi.org/10.1007/s00442-001-0865-5 Hakkarainen, H., Mykrä, S., Kurki, S., Korpimäki, E., Ni- kula, A. & Koivunen, V. 2003: Habitat composition as a determinant of reproductive success of Tengmalm’s owls under fluctuating food conditions. — Oikos 100: 162–171. https://doi.org/10.1034/j.1600-0706.2003. 11906.x Halonen, M., Mappes, T., Meri, T. & Suhonen, J. 2007: In- fluence of snow cover on food hoarding in pygmy owls Glaucidium passerinum. — Ornis Fennica 84: 105– 111. https://ornisfennica.journal.fi/article/view/133686 Hijmans, R.J. & van Etten, J. 2012: raster: Geographic anal- ysis and modelling with raster data. R package version 2.5–8. http://CRAN.R-project.org/package=raster Huitu, O., Norrdahl, K. & Korpimäki, E. 2003: Landscape effects on temporal and spatial properties of vole popu- lation fluctuations. — Oecologia 135: 209–220. https:// doi.org/10.1007/s00442-002-1171-6 Iglesias-Carrasco, M., Brookes, S., Kruuk, L.E.B. & Head, M.L. 2020: The effects of competition on fitness de- pend on the sex of both competitors. — Ecology and Evolution 10: 9808–9826. https://doi.org/10.1002/ ece3.6620 Ishikawa, K. & Watanuki, Y. 2002: Sex and individual dif- ferences in foraging behavior of Japanese cormorants in years of different prey availability. — Journal of Ethology 20: 49–54. https://doi.org/10.1007/s10164- 002-0053- z Jaeger, R.G., Nishikawa, K.C.B. & Barnard, D.E. 1983: Foraging tactics of a terrestrial salamander: Costs of territorial defence. — Animal Behaviour 31: 191–198. https://doi.org/10.1016/S0003-3472(83)80188-2 Jetz, W., Carbone, C., Fulford, J. & Brown, J.H. 2004: The Scaling of Animal Space Use. — Science 306: 266– 268. https://doi.org/10.1126/science.1102138 Kellomäki, E. 1977: Food of the pygmy owl Glaucidium passerinum in the breeding season. — Ornis Fennica 54: 1–29. https://ornisfennica.journal.fi/article/ view/132921 Korpimäki, E. 1987: Dietary shifts, niche relationships and reproductive output of coexisting Kestrels and Long eared Owls. — Oecologia (Berlin) 74: 277–285. https:// doi.org/10.1007/BF00379371 Korpimäki, E., Norrdahl, K. & Rinta-Jaskari, T. 1991: Responses of stoats and least weasels to fluctuating vole abundances: is the low phase of the vole cycle due to mustelid predation? — Oecologia 88: 552–561. https://doi.org/10.1007/BF00317719 Korpimäki, E., Koivunen, V. & Hakkarainen, H. 1996: Microhabitat use and behavior of voles under weasel and raptor predation risk: predator facilitation? — Be- havioral Ecology 7: 30–34. https://doi.org/10.1093/be- heco/7.1.30 Korpimäki, E., Norrdahl, K., Huitu, O. & Klemola, T. 2005: Predator-induced synchrony in population oscillations of coexisting small mammal species. — Proceedings of the Royal Society B: Biological Sciences 272: 193– 202. https://doi.org/10.1098/rspb.2004.2860 Kor- pimäki, E. & Hakkarainen, H. 2012: The Boreal owl: ecology, behaviour and conservation of a forest-dwell- ing predator. — Cambridge University Press, Cam- bridge. https://doi.org/10.1017/CBO9780511844164 Korpimäki, E., Hongisto, K., Masoero, G. & Laaksonen, T. 2020: The difference between generalist and specialist: the effects of wide fluctuations in main food abundance on numbers and reproduction of two co-existing preda- tors. — Journal of Avian Biology 51: 1–13. https://doi. org/https://doi.org/10.1111/jav.02508 Krüger, O. 2005: The evolution of reversed sexual size di- morphism in hawks, falcons and owls: a comparative study. — Evolutionary Ecology 19: 467–486. https:// doi.org/10.1007/s10682-005-0293-9 Lagerström, M. & Syrjänen, J. 1990: Ageing Pygmy Owls. — Lintumies 25: 291–194. (In Finnish with English summary) Marchetti, K., & Price, T. 1989: Differences in the foraging of juvenile and adult birds: the importance of develop- mental constraints. — Biological Reviews 64: 51–70. https://doi.org/10.1111/j.1469-185X.1989.tb00638.x Massemin, S., Korpimäki, E. & Wiehn, J. 2000: Reversed sexual size dimorphism in raptors: evaluation of the hypothesis in kestrels breeding in a temporally chang- ing environment. — Oecologia 124: 26–32. https://doi. org/10.1007/s004420050021 Masoero, G., Morosinotto, C., Laaksonen, T. & Korpimäki, E. 2018: Food hoarding of an avian predator: sex- and age-related differences under fluctuating food condi- tions. — Behavioral Ecology and Sociobiology 72: 159. https://doi.org/10.1007/s00265-018-2571-x Masoero, G., Laaksonen, T., Morosinotto, C. & Korpimäki, E. 2020: Age and sex differences in numerical respons- es, dietary shifts, and total responses of a generalist predator to population dynamics of main prey. — Oec- ologia 192: 699–711. https://doi.org/10.1007/s00442- 020-04607-x Mikusek, R. 2019: The role of caches in the Eurasian Pyg- my Owl Glaucidium passerinum during the breeding season. — Ornis Polonica 60: 1–15. http://ornis-polon- ica.pl/_pdf/OP-60-1-Mikusek.pdf Miller, R.S. 1967: Pattern and process in competition. — Koivisto et al.: Density drives sex-specific spatial distribution and hoarding in Pygmy Owls 186 Advances in Ecological Research 4: 1–74. Mills, R., Taylor, G.K. & Hemelrijk, C.K. 2019: Sexual size dimorphism, prey morphology and catch success in re- lation to flight mechanics in the peregrine falcon: a sim- ulation study. — Journal of Avian Biology 2019: e01979. https://doi.org/10.1111/jav.01979 Morosinotto, C., Thomson, R.L. & Korpimäki, E. 2010: Habitat selection as an antipredator behaviour in a mul- ti‐predator landscape: all enemies are not equal. — Journal of Animal Ecology 79: 327–333. https://doi. org/10.1111/j.1365-2656.2009.01638.x Morosinotto, C., Villers, A., Thomson, R.L., Varjonen, R. & Korpimäki, E. 2017a: Competitors and predators alter settlement patterns and reproductive success of an in- traguild prey. — Ecological Monographs 87: 4–20. https://doi.org/10.1002/ecm.1238 Morosinotto, C., Villers, A., Varjonen, R. & Korpimäki, E. 2017b: Food supplementation and predation risk in harsh climate: interactive effects on abundance and body condition of tit species. — Oikos 126: 863–873. https://doi.org/10.1111/oik.03476. Oddie, K.R. 2000: Size matters: Competition between male and female great tit offspring. — Journal of Animal Ecology 69: 903–912. https://doi.org/10.1046/ j.1365-2656.2000.00438.x Pérez-Camacho, L., García-Salgado, G., Rebollo, S., Martínez-Hesterkamp, S. & Fernández-Pereira, J.M. 2015: Higher reproductive success of small males and greater recruitment of large females may explain strong reversed sexual dimorphism (RSD) in the northern gos- hawk. — Oecologia 177: 379–387. https://doi. org/10.1007/s00442-014-3146-9 Pérez-Camacho, L., Martínez-Hesterkamp, S., Rebollo, S., García-Salgado, G. & Morales-Castilla, I. 2018: Struc- tural complexity of hunting habitat and territoriality increase the reversed sexual size dimorphism in diurnal raptors. — Journal of Avian Biology 49: e01745. https://doi.org/10.1111/jav.01745 Pulliam, H.R. & Danielson, B.J. 1991: Sources, sinks, and habitat selection: a landscape perspective on population dynamics. — American Naturalist 137: 50–66. https:// doi.org/10.1086/285139 R Core Team 2022: R: A language and environment for sta- tistical computing. — R Foundation for Statistical Computing. Reigert, J. & Fuchs, R. 2011: Fidelity to roost sites and diet composition of wintering male urban Common Kes- trels Falco tinnunculus. — Acta Ornithology 46: 183– 189. https://doi.org/10.3161/000164511X625955 Ritchie, E.G. & Johnson, C.N. 2009: Predator interactions, mesopredator release and biodiversity conservation. — Ecology Letters 12: 982–998. https://doi. org/10.1111/j.1461-0248.2009.01347.x Schmidt-Nielsen, K. & Knut, S.N. 1984: Scaling: why is animal size so important? — Cambridge university press, Cambridge. Schoener, T.W. 1974: Resource partitioning in ecological communities. — Science 185: 27–39. https://doi. org/10.1126/science.185.4145.27 Schoener, T.W. 1983: Field experiments on interspecific competition. — American Naturalist 122: 240–285. https://www.jstor.org/stable/2461233 Schönn, S. 1980: Der Sperlingskauz. — Die Neue Bre- hm-Bücherei, Wittenberg-Luthesstadt. (In German) Sih, A., Crowley, P., McPeek, M., Petranka, J. & Strohmei- er, K. 1985: Predation, competition and prey communi- ties: a review of field experiments. — Annual Review of Ecology, Evolution, and Systematics 16: 269–311. https://doi.org/10.1146/annurev.es.16.110185.001413 Smallegange, I.M. & van der Meer, J. 2006: Interference from a game theoretical perspective: shore crabs suffer most from equal competitors. — Behavioral Ecology 18: 215–221. https://doi.org/10.1093/beheco/arl071 Smith, R.D. & Metcalfe, N.B. 1994: Age, Sex and Prior Site Experience Have Independent Effects on the Foraging Success of Wintering Snow Buntings. — Behaviour 129: 99–111. https://doi.org/10.1163/156853994X00370 Solheim, R. 1984a: Caching behaviour, prey choice and surplus killing by pygmy owls Glaucidium passerinum during winter, a functional response of a generalist predator. — Annales Zoologici Fennici 21: 301–308. https://www.jstor.org/stable/23734162 Solheim, R. 1984b: Breeding biology of the pygmy owl Glaucidium passerinum in two biogeographical zones in southeastern Norway. — Annales Zoologici Fennici 21: 295–300. https://www.jstor.org/stable/23734161 Strøm, H. & Sonerud, G.A. 2001: Home range and habitat selection in the pygmy owl Glaucidium passerinum. — Ornis Fennica 78: 145–158. https://ornisfennica.jour- nal.fi/article/view/133558 Suhonen, J., Halonen, M., Mappes, T. & Korpimäki, E. 2007: Interspecific competition limits larders of pygmy owls. — Journal of Avian Biology 38: 630–634. https:// doi.org/10.1111/j.2007.0908-8857.03960.x Svanbäck, R. & Bolnick, D.I. 2007: Intraspecific competi- tion drives increased resource use diversity within a natural population. — Proceedings of the Royal Socie- ty B: Biological Sciences 274: 839–844. https://doi. org/10.1098/rspb.2006.0198 Svanbäck, R., Eklöv, P., Fransson, R. & Holmgren, K. 2008: Intraspecific competition drives multiple species resource polymorphism in fish communities. — Oikos 117: 114–124. https://doi.org/10.1111/j.2007.0030- 1299.16267.x Taylor, I.R. 1994: Barn Owls. Predator-prey relationships and conservation. — Cambridge University Press, Cambridge. Templeton, C.N., Greene, E. & Davis, K. 2005: Allometry of Alarm Calls: Black-Capped Chickadees Encode In- formation About Predator Size. — Science 308: 1934. https://doi.org/10.1126/science.1108841 Terraube, J., Villers, A., Poudré, L., Varjonen, R. & Kor- pimäki, E. 2017: Increased autumn rainfall disrupts predator-prey interactions in fragmented boreal forests. 187 ORNIS FENNICA Vol.100, 2023 — Global Change Biology 23: 1361–1373. https://doi. org/doi.org/10.1111/gcb.13408 Valeix, M., Chamaillé-Jammes, S. & Fritz, H. 2007: Inter- ference competition and temporal niche shifts: ele- phants and herbivore communities at waterholes. — Oecologia 153: 739–748. https://doi.org/10.1007/ s00442-007-0764-5 Vander Wall, S.B. 1990: Food Hoarding in Animals. — University of Chicago Press, Chicago. https://doi. org/10.1016/0169-5347(90)90034-B Vander Wall, S.B. & Jenkins, S.H. 2003: Reciprocal pilfer- age and the evolution of food-hoarding behaviour. — Behavioral Ecology 14: 656–667. https://doi. org/10.1093/beheco/arg064 Wikelski, M. & Thom, C. 2000: Marine iguanas shrink to survive El Niño. — Nature 403: 37–38. https://doi. org/10.1038/47396 Wunderle, J.M. Jr 1991: Age-specific foraging proficiency in birds. — In Current ornithology vol. 8 (Ed. Power, D.M.): 273–324, Plenum Publishing Corporation, New York. Ziv, Y., Abramsky, Z., Kotler, B.P. & Subach, A. 1993: In- terference competition and temporal and habitat parti- tioning in two gerbil species. — Oikos 66: 237–246. https://doi.org/10.2307/3544810 Online supplementary material Supplementary material available in the online version (https://doi.org/10.51812/of.130326) includes Tables S1–S2 with information on model selection.