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It is not clear whether animals consistently change their home ranges in response to density reduction. This is important to understand for better management of pest species where sustained control is required. Our objective was to measure whether home ranges of Australian brushtail possums (Trichosurus vulpecula) change following density reduction, using global positioning system (GPS) tracking. We experimentally reduced the densities of 2 populations (1 high-density at 7 possums/ha and 1 low-density at 1.5 possums/ha) and did not manipulate another population. We then monitored home ranges of individual possums. The high-density manipulated population had a significant increase in home-range size and overlap within 5 weeks following reduction, whereas the other 2 populations did not. This research suggests that changes in possum home ranges following control are likely influenced by the initial density of the pest population.

Previous breeding-season studies of threatened New Zealand falcons (Falco novaeseelandiae) in plantation forests have suggested that falcons benefit when harvesting creates a mosaic of differently aged stands, especially where young and mature tree stands are adjacent. Thus, changes in the rate and pattern of harvesting may affect habitat heterogeneity by altering the size and distribution of forest patches. We sought to determine guidelines for harvesting that would most benefit falcons by increasing the carrying capacity of the forest for falcons. We used radio-tracking to determine the home-range sizes of non-breeding falcons over 3 seasons and compared winter home-range overlap in the most-selected land cover types by falcons (mature-young edges and open patches) with other land cover types. The distribution of open patches and edges between mature stands and recently cleared areas affected falcon home ranges, home-range overlap, and the likelihood of nesting. Specifically, home ranges were smaller as the density of edges and percentage of open patch increased, and there was greater home-range overlap between individuals in the most-selected land cover types. Numbers of falcons decreased as the size of open patches increased, concomitant with a decrease in edge size, the number of edge borders, and the number of open patches. The likelihood of nesting also decreased as open patch size increased. Our results indicate that smaller open patches spread through a forest, maximizing the amount of mature-young edges, will favor smaller home ranges and therefore potentially greater numbers of falcons. We recommend harvesting protocols that ensure that open patches (0–3-yr-old stands) are <4km² in size and retain at least small stands of mature pine to maintain a high density of edges. Similar protocols may increase the carrying capacity for other species occurring in managed systems involving fragmented landscapes or small reserves.

Animal space use is affected by spatio-temporal variation in food availability and/or population density and varies among individuals. This inter-individual variation in spacing behaviour can be further influenced by sex, body condition, social dominance, and by the animal’s personality. We used capture-mark-recapture and radio-tracking to examine the relationship between space use and personality in Eurasian red squirrels (Sciurus vulgaris) in three conifer forests in the Italian Alps. We further explored to what extent this was influenced by changes in food abundance and/or population density. Measures of an individual’s trappability and trap diversity had high repeatability and were used in a Principal Component Analysis to obtain a single personality score representing a boldness-exploration tendency. Males increased home-range size with low food abundance and low female density, independent of their personality. However, bolder males used larger core-areas that overlapped less with other males than shy ones, suggesting different resource (food, partners) utilization strategies among personality types. For females, space use-personality relationships varied with food abundance, and bolder females used larger home ranges than shy ones at low female density, but the trend was opposite at high female density. Females’ intrasexual core-area overlap was negatively related to body mass, with no effect of personality. We conclude that relationships between personality traits and space use in free-ranging squirrels varied with sex, and were further influenced by spatio-temporal fluctuations in food availability. Moreover, different personality types (bold-explorative vs. shy) seemed to adopt different space-use strategies to increase access to food and/or partners.

Tracking studies for invasive lionfish (Pterois volitans and P. miles) in the Western Atlantic can provide key information on habitat use to inform population control, but to date have likely underestimated home range size and movement due to constrained spatial and temporal scales. We tracked 35 acoustically tagged lionfish for >1 yr (March 2018–May 2019) within a 35 km² acoustic array in Buck Island Reef National Monument, St. Croix, US Virgin Islands (an area 10× larger than previous studies). Tracking lionfish at this scale revealed that home range size is 3–20 times larger than previously estimated and varies more than 8-fold across individuals (~48 000–379 000 m²; average: 101 000 m²), with estimates insensitive to assumptions about potential mortality for low-movement individuals. Lionfish move far greater distances than previously reported, with 37% of fish traveling >1 km from the initial tagging site toward deeper habitats, and 1 individual moving ~10 km during a 10 d period. Movement rates, home range size, and maximum distance traveled were not related to lionfish size (18–35 cm total length) or lunar phase. Lionfish movement was lowest at night and greatest during crepuscular periods, with fish acceleration (m s−2) increasing with water temperature during these times. Our results help reconcile observed patterns of rapid recolonization following lionfish removal, and suggest complex drivers likely result in highly variable patterns of movement for similarly sized fish occupying the same habitat. Culling areas ≥ the average lionfish home range size identified here (i.e. ~10 ha) or habitat patches isolated by ≥ ~180 m (radius of average home range) may minimize subsequent recolonization. If the shallow–deep long-distance movements observed here are unidirectional, mesophotic habitats may require culling at relatively greater frequencies to counteract ongoing migration.

Home range is the area traversed by an animal in its normal activities. The size of home ranges is thought to be tightly linked to body size, through size effect on metabolic requirements. Due to the structure of Eltonian food pyramids, home range sizes of carnivores are expected to exceed those of herbivorous species. The habitat may also affect home range size, with reduced costs of locomotion or lower food abundance in, for example, aquatic habitats selecting for larger home ranges. Furthermore, home range of males in polygamous species may be large due to sexual selection for increased reproductive output. Comparative studies on home range sizes have rarely been conducted on ectotherms. Because ectotherm metabolic rates are much lower than those of endotherms, energetic considerations of metabolic requirements may be less important in determining the home range sizes of the former, and other factors such as differing habitats and sexual selection may have an increased effect. We collected literature data on turtle home range sizes. We used phylogenetic generalized least squares analyses to determine whether body mass, sex, diet, habitat and social structure affect home range size. Turtle home range size increases with body mass. However, body mass explains relatively little of the variation in home range size. Aquatic turtles have larger home ranges than semiaquatic species. Omnivorous turtles have larger home ranges than herbivores and carnivores, but diet is not a strong predictor. Sex and social structure are unrelated to home range size. We conclude that energetic constraints are not the primary factor that determines home range size in turtles, and energetic costs of locomotion in different habitats probably play a major role.

African savanna elephants are a highly mobile species that ranges widely across the diversity of ecosystems they inhabit. In xeric environments, elephant movement patterns are largely dictated by the availability of water and suitable forage resources, which can drive strong seasonal changes in their movement behavior. In this study, we analyzed a unique movement dataset from 43 collared elephants, collected over a period of 10 years, to assess the degree to which seasonal changes influences home range size of elephants in the semi‐arid, Laikipia‐Samburu ecosystem of northern Kenya. Auto‐correlated Kernel Density Estimation (AKDE) was used to estimate elephants' seasonal home range size. For each individual elephant, we also calculated seasonal home range shifts, as the distance between wet season home range centroids and dry season home range centroids. Core areas (50% AKDE isopleths) of all individual elephants ranged from 3 to 1743 km2 whereas total home range sizes (the 95% AKDE isopleths) ranged between 15 and 10,677 km2. Core areas and home range sizes were 67% and 61% larger, respectively, during the wet season than during the dry season. On average, the core area centroids for all elephants were 17 km away from the nearest river (range 0.2–150.3 km). Females had their core areas closer to the river than males (13.5 vs. 27.5 km). Females differed from males in their response to seasonal variation. Specifically, females tended to occupy areas farther from the river during the wet season, while males occupied areas further from the river during the dry season. Our study highlights how elephants adjust their space use seasonally, which can be incorporated into conservation area planning in the face of increased uncertainty in rainfall patterns due to climate change. This manuscript presents an analysis of the how elephant adjust their space use seasonally. In particular, the paper investigates the variation in home range sizes and home range shifts across seasons. Our results exhibit the importance of tailored conservation strategies that would ensure the longevity of elephant populations while safeguarding landscape connectivity and crucial movement corridors, addressing both immediate and long‐term threats.

Brain lateralization is a widespread phenomenon although its expression across primates is still controversial due to the reduced number of species analyzed and the disparity of methods used. To gain insight into the diversification of neuroanatomical asymmetries in non-human primates we analyze the endocasts, as a proxy of external brain morphology, of a large sample of New World monkeys and test the effect of brain size, home range and group sizes in the pattern and magnitude of shape asymmetry. Digital endocasts from 26 species were obtained from MicroCT scans and a set of 3D coordinates was digitized on endocast surfaces. Results indicate that Ateles, Brachyteles, Callicebus and Cacajao tend to have a rightward frontal and a leftward occipital lobe asymmetry, whereas Aotus, Callitrichinae and Cebinae have either the opposite pattern or no directional asymmetry. Such differences in the pattern of asymmetry were associated with group and home range sizes. Conversely, its magnitude was significantly associated with brain size, with larger-brained species showing higher inter-hemispheric differences. These findings support the hypothesis that reduction in inter-hemispheric connectivity in larger brains favors the lateralization and increases the structural asymmetries, whereas the patterns of shape asymmetry might be driven by socio-ecological differences among species.

Large herbivores respond to fluctuations in predation and hunting risk. The temporal scale of risk heterogeneity affects behavioral responses and determines the usefulness of metrics to quantify them. We present a conceptual framework to link anti-predator responses to risk fluctuations and appropriate metrics, based on temporal scale. We applied this framework to investigate movement responses of roe deer (Capreolus capreolus) to hunting risk, measured using movement rate and home range size. Because movements are also affected by reproductive phases, we considered potential effects of the rut in parallel to hunting risk. We compared movements of male and female roe deer in a protected site versus 2 hunted sites during and outside the hunting season and rut. We detected differences in movement rates in response to different hunting management practices. We did not detect effects for hunting regimes or between sexes during the rut when using home range size as the response variable. During the hunting season, movement rates were lower in the hunted sites than in the protected site, irrespective of sex. We did not observe differences in movement rates among sites outside of the hunting season. Males had higher movement rates than females during the rut in only 1 site. Our findings supported the hypothesis that roe deer decrease movements when exposed to high hunting risk. The effect of the rut on movements was negligible except for 1 study site. We suggest that movement rate is a more useful metric than home range size for assessing movement responses to hunting.

Ranging behavior, including home range use and daily travel distance, provides valuable information on the behavioral responses of primates to their habitats. We evaluated the ranging behavior of wild silvery lutungs (Trachypithecus cristatus) inhabiting a coastal forest in West Sumatra, Indonesia, for 614 h over 15 months in 2018–2021, focusing on the relationships between ranging behavior and activity budgets, dietary composition, and food availability. The annual home range was 8.1 ha (minimum convex polygon) and 11.7 ha (95% kernel), and the mean (± standard deviation [SD]) daily travel distance was 926 ± 385 m. Daily travel distance showed a positive correlation with percent resting and negative correlations with percent feeding and moving. Furthermore, daily travel distance was correlated positively with percent young leaf feeding and negatively with percent mature leaf feeding, ripe fruit feeding, and dietary diversity. In contrast, home range size did not vary significantly across the study period, and we found few significant correlations between home range size and dietary composition or activity budget. The longer daily travel distances in food scarce season are likely due to the lutungs needing to travel further to find trees bearing young leaves. We conclude that the silvery lutungs’ ranging behavior is linked to their high-risk, high-return strategy.

The spatial distribution of animals has consequences for nutrition, predator–prey dynamics, spread of diseases, and population dynamics in general. Animals must establish a home range to secure adequate resources to fuel their energy needs. Home ranges, therefore, are temporally and spatially dynamic, given the changing requirements of an animal and the availability of resources on the landscape. We used data from two populations of bighorn sheep with contrasting population dynamics following pneumonia epizootics and different habitat quality on their summer range to test the hypothesis that the distribution and size of home ranges are influenced by environmental conditions and reproductive status. We used a combination of data from 768 vegetation transects and remotely sensed metrics to index forage quality of consecutive biweekly home ranges for 27 bighorn sheep, June–August 2019–2021. There were population differences in home range dynamics that were consistent with resource limitations in the population declining in abundance. Animals in both populations increased the size of their home range through the summer in association with declining forage quality indexed by plant phenology. Furthermore, animals in the Whiskey Mountain population without offspring had home ranges more than twice the size of animals with offspring, whereas there were no differences in the home range size between animals with and without offspring in Jackson. We demonstrated that limitations young offspring impose on space use of a mother may have consequences for animals living where larger home ranges are needed to secure adequate resources—sheep on Whiskey Mountain had to travel 1000 m from escape terrain to access the same amount of biomass that the Jackson sheep could access directly adjacent to escape terrain. Forage quality and availability influence movement and space use. In the presence of disease, movement and space use may influence pathogen transmission and persistence. Thus, forage availability may play an indirect role in population dynamics in the presence of disease, which is another line of evidence for how environmental and nutritional conditions may influence population dynamics when coping with disease.