Home range and habitat use by the sable<Emphasis Type="Italic"> Martes zibellina brachyura</Emphasis> in a Japanese cool-temperate mixed forest

Home range and habitat use of the sable Martes zibellina brachyura were studied in a cool-temperate mixed forest in northernmost Japan. In both sexes, some sables showed a wide range of migration without establishing home ranges and the others had home ranges of 0.50–1.78 km² (mean: 1.12±SD 0.495 km², n =6) which were not significantly correlated with body weight or age. The analysis of canine tooth annuli revealed that the maximum age was 5.5 years. The home ranges of some sables overlapped so extensively that the home ranges and even the core areas did not appear exclusive to other sables. We determined resting sites and foraging routes in snow in winter. Comparison of vegetation at the resting sites and foraging routes with habitat availability suggested that the sables preferred resting in dense-tree forests with many tree species and debris probably in order to avoid predators (red foxes) and strong wind and foraging in forests of climax succession which are usually rich in their prey such as voles and mice.     

Space use and resting site selection of red foxes (<Emphasis Type="Italic">Vulpes vulpes</Emphasis>) living near villages and small towns in Southern Germany

In 2005–2008, we radio-tracked 17 foxes in rural areas of Southern Germany. The mean home range size was 76.6 ha (95% MCP) or 138.9 ha (95% fixed kernel), and the built-up area formed an integral part of the home range. Home ranges of juvenile foxes were significantly smaller than home ranges of adult foxes. Gender-specific differences among adult foxes were not established. A minimum population density of 2.7 foxes per km² and summer densities of up to 13.4 foxes per km² were calculated. Therefore, the fox density was three to eight times higher than that of strictly rural foxes. Daytime resting sites of foxes were mostly found in forests (62.2%) and reedbed areas (20.6%). Of the resting sites, 14.8% were situated inside settlements, in fallow gardens or gardens of residents. During the day, foxes exhibited habitat preferences for forests and reedbed areas. A habitat structure that offers plenty of cover or dense vegetation is essential for its selection as a safe resting site. If this basic requirement is fulfilled, foxes also choose resting sites within settlements, and are not disturbed by human presence.     

Habitat selection and home range in the Blanford's fox,Vulpes cana: compatibility with the resource dispersion hypothesis

Summary This paper presents analyses of habitat-use and home range size in the Blanford's fox. We predicted, from the resource dispersion hypothesis (RDH), that home ranges would encompass similar areas of combined fruitful habitats, but widely different areas of useless habitats, and thus that home ranges would be larger where such fruitful patches are fragmented and widely dispersed. Home range estimates of 0.5–2.0 km² were calculated for 16 adult Blanford's foxes, using three different methods. There were no significant differences in home range size between sexes or study sites. One habitat, dry creekbed, was the most frequently visited in all home ranges. Dry creekbed provided abundant prey for the foxes and only sparse cover for their predators. Both the available area of creekbed in each range, and the area of creekbed patches that was used by the foxes, were independent of home range size. However, the variance in home range size was explained by the mean distance between the main denning area and the most frequently used patches of creekbed. These results are in accord with some predictions of the resource dispersion hypothesis.     

Living in the suburbs: Space use by vervet monkeys (Chlorocebus pygerythrus) in an eco‐estate,South Africa

We examined vervet monkey (Chlorocebus pygerythrus) space use using GPS/UHF telemetry data from 10 vervet monkeys across six troops over 9 months within a 420 ha suburban eco‐estate. We documented a mean home range of 0.99 km² (95% MCP) and 1.07 km² (95% KDE) for females (n = 6), 1 km² (95% MCP) and 1.50 km² (95% KDE) for males (n = 4) and 0.87 km² (95% MCP) and 1.12 km² (95% KDE) for troops (n = 6), respectively, indicating that males and larger troops had larger home ranges. These relatively small home ranges included shared territorial boundaries and high home range overlap. Vervet monkey movements indicated higher morning activity levels, and habitat selection indicated significantly more use of golf course, urban residential and forest, thicket and woodland areas, and avoidance of wetland, grassland and shrub, and urban built‐up areas. Our results suggest that modified habitat use by vervet monkeys is a consequence of behavioural facilitation to access highly available food resources, thereby facilitating their persistence in green spaces in urban areas of South Africa. Conflict management is dependent on the conservation of sufficient natural habitats and food resources, to minimise their dependence on anthropogenic supplementary food resources and consequently reduce human–monkey conflict.     

Home ranges in red fox: territoriality diminishes with increasing area

Red foxVulpes vulpes (Linnaeus, 1758) are generally regarded as strictly territorial animals, inhabiting distinct and well-separated ranges. The home ranges of these predators can vary in size from a few dozen hectares to as much as 20–30 km². Because it seemed impossible that foxes could defend areas so different in size with the same intensity, the published data were analysed in order to see how changes in home range size could affect the following parameters: home range overlap, the area visited daily and the distance travelled by animals during 24 h. It was found that the overlap between fox families (groups) occupying large ranges was much greater than between foxes living in small ranges. The ratio of the area visited daily to the seasonal home range size was greater in small ranges than in large ones. No significant correlation was found between the mean distance moved daily and home range size (r = −0.118,p = 0.75). These results suggest different patterns of the use of space and differences in territorial defence by red foxes inhabiting large and small ranges. The implications of home range overlap and intensity of contacts between foxes occupying neighbouring ranges for the spread of disease are discussed. The significant overlap between large ranges found in this paper is discussed in the light of Andrzejewski’s (2002) home range concept.

     

Home range size of adult Indo‐Pacific bottlenose dolphins (Tursiops aduncus) in a coastal and estuarine system is habitat and sex‐specific

This study examined sex‐specific differences in home range size of adult Indo‐Pacific bottlenose dolphins off Bunbury, Western Australia. We applied a new kernel density estimation approach that accounted for physical barriers to movements. A Bayesian mixture model was developed to estimate a sex effect in home range size with latent group partitioning constrained by association data. A post hoc analysis investigated group partitioning relating to the proportion of time spent in open vs. sheltered waters. From 2007 to 2013, photographic‐identification data were collected along boat‐based systematic transect lines (n = 586). Analyses focused on adult dolphins of known sex (sighted ≥ 30 times; n = 22 males and 34 females). The 95% utilization distributions of males varied between 27 and 187 km² (; 94.8 ± 48.15) and for females between 20 and 133 km² (65.6 ± 30.9). The mixture model indicated a 99% probability that males had larger home ranges than females. Dolphins mostly sighted in open waters had larger home ranges than those in sheltered waters. Home ranges of dolphins sighted in sheltered waters overlapped with areas of highest human activity. We suggest that sex differences in home ranges are driven by male mating strategies, and home range size differences between habitats may be influenced by prey availability and predation risk.     

Adaptable Neighbours: Movement Patterns of GPS-Collared Leopards in Human Dominated Landscapes in India

Understanding the nature of the interactions between humans and wildlife is of vital importance for conflict mitigation. We equipped five leopards with GPS-collars in Maharashtra (4) and Himachal Pradesh (1), India, to study movement patterns in human-dominated landscapes outside protected areas. An adult male and an adult female were both translocated 52 km, and exhibited extensive, and directional, post release movements (straight line movements: male  = 89 km in 37 days, female  = 45 km in 5 months), until they settled in home ranges of 42 km² (male) and 65 km² (female). The three other leopards, two adult females and a young male were released close to their capture sites and used small home ranges of 8 km² (male), 11 km² and 15 km² (females). Movement patterns were markedly nocturnal, with hourly step lengths averaging 339±9.5 m (SE) during night and 60±4.1 m during day, and night locations were significantly closer to human settlements than day locations. However, more nocturnal movements were observed among those three living in the areas with high human population densities. These visited houses regularly at nighttime (20% of locations <25 m from houses), but rarely during day (<1%). One leopard living in a sparsely populated area avoided human settlements both day and night. The small home ranges of the leopards indicate that anthropogenic food resources may be plentiful although wild prey is absent. The study provides clear insights into the ability of leopards to live and move in landscapes that are extremely modified by human activity.     

Home on the range: spatial ecology of loggerhead turtles in Atlantic waters of the USA

Aim Although satellite tracking has yielded much information regarding the migrations and habitat use of threatened marine species, relatively little has been published about the environmental niche for loggerhead sea turtles Caretta caretta in north‐west Atlantic waters. Location North Carolina, South Carolina and Georgia, USA. Methods We tracked 68 adult female turtles between 1998 and 2008, one of the largest sample sizes to date, for 372.2 ± 210.4 days (mean ± SD). Results We identified two strategies: (1) ‘seasonal’ migrations between summer and winter coastal areas (n = 47), although some turtles made oceanic excursions (n = 4) and (2) occupation of more southerly ‘year‐round’ ranges (n = 18). Seasonal turtles occupied summer home ranges of 645.1 km² (median, n = 42; using α‐hulls) predominantly north of 35 ° latitude and winter home ranges of 339.0 km² (n = 24) in a relatively small area on the narrow shelf off North Carolina. We tracked some of these turtles through successive summer (n = 8) and winter (n = 3) seasons, showing inter‐annual home range repeatability to within 14.5 km of summer areas and 10.3 km of winter areas. For year‐round turtles, home ranges were 1889.9 km². Turtles should be tracked for at least 80 days to reliably estimate the home range size in seasonal habitats. The equivalent minimum duration for ‘year‐round’ turtles is more complex to derive. We define an environmental envelope of the distribution of North American loggerhead turtles: warm waters (between 18.2 and 29.2 °C) on the coastal shelf (in depths of 3.0–89.0 m). Main conclusions Our findings show that adult female loggerhead turtles show predictable, repeatable home range behaviour and do not generally leave waters of the USA, nor the continental shelf (< 200m depth). These data offer insights for future marine management, particularly if they were combined with those from the other management units in the USA.     

Home ranges, movements, and activity of wolves (Canis lupus) in the Dalmatian part of Dinarids, Croatia

Home-range sizes, movements, and daily activity of wolves (Canis lupus L. 1758) were studied in Dalmatia, Croatia in 1998–2001. The total home ranges (100% MCP) of two packs were 160 km² and 141 km², mean=150.5 km². Core areas (50% kernel) were 26.2 km² and 3.3 km², respectively. Differences in core area sizes were influenced by human activity—hunting and sheep grazing. Compared with random locations, wolf locations were closer to the nearest water source (mean=937 m) and farther from houses (mean=653 m). Wolves were significantly more active during the night than during the day (activity indexes were 0.53 vs. 0.35), and night activity was higher during summer (0.58), and lower during winter (0.48). A correlation was found between distances traveled and activity index (r=0.58, p=0.003). Home range, seasonal variations in home-range size, habitat use, and activity of wolves in Dalmatia were oriented to make the compromise from danger of proximity to humans and also to benefit from human-related food sources.     

Home ranges and densities of medium-sized carnivores in south-east Finland, with special reference to rabies spread

Home ranges and densities of medium-sized carnivores were studied in south-east Finland by radio tracking. The species studied included potential vectors of rabies: the raccoon dogNyctereutes procyonoides (Gray, 1834), red foxVulpes vulpes (Linnaeus, 1758), European badgerMeles meles (Linnaeus, 1758) and domestic catFelis silvestris catus (Schreber, 1777). Home ranges of badgers were largest (mean 14.7 km²) and those of cats smallest (1.5 km²). Home ranges overlapped largely, both within and between species. Most home ranges were larger and population densities lower in south-east Finland compared with those in Western Europe. The pooled density of medium-sized carnivores with overlapping home ranges was, however, high, which may indicate a high risk of a rabies epizootic in this multi-host community. Rabies might also spread rapidly to new areas, because of the large home ranges and, consequently, long dispersal distances.     

Dispersal of Yearling Pronghorns in Western South Dakota

Abstract: We captured and radiocollared 57 pronghorn (Antilocapra americana) fawns in western South Dakota, USA, during May 2002–2003 and radiotracked them through 15 months of age, by which time all surviving individuals had established a permanent home range. We classified 56% (n = 19) of fawns as dispersers and 44% (n = 15) as residents. Eighty-four percent (n = 16) of dispersers departed natal home ranges in late October and occupied winter home ranges for 102–209 days before dispersing to permanent home ranges during April 2003 and 2004. Dispersal distances from natal ranges to permanent home ranges varied from 6.2–267.0 km. Winter home-range sizes for all individual pronghorns varied from 39.4–509.6 km. Permanent home-range size for all individuals varied from 15.5–166.1 km². Mean 95% permanent home-range size differed (P = 0.06) between residents (x̄ = 97.3 ± 15.1 km²) and dispersers (x̄ = 48.6 ± 16.0 km²), but was similar (P = 0.97) among sexes. Mean dispersal distance from natal to permanent home ranges was similar (P = 0.35) for males (x̄ = 54.2 ± 21.0 km) and females (x̄ = 26.3 ± 19.9 km). We suggest that habitat quality (i.e., patchiness) and pronghorn density, in part, stimulated dispersal. We hypothesize that as habitat patch size decreases, home range sizes and distance traveled during predispersal and dispersal movements by pronghorns will increase.     

Multi Year Observations Reveal Variability in Residence of a Tropical Demersal Fish,Lethrinus nebulosus: Implications for Spatial Management

Off the Ningaloo coast of North West Western Australia, Spangled Emperor Lethrinus nebulosus are among the most highly targeted recreational fish species. The Ningaloo Reef Marine Park comprises an area of 4,566 km² of which 34% is protected from fishing by 18 no-take sanctuary zones ranging in size from 0.08–44.8 km². To better understand Spangled Emperor movements and the adequacy of sanctuary zones within the Ningaloo Reef Marine Park for this species, 84 Spangled Emperor of a broad spectrum of maturity and sex were tagged using internal acoustic tags in a range of lagoon and reef slope habitats both inside and adjacent to the Mangrove Bay Sanctuary zone. Kernel Utilisation Distribution (KUD) was calculated for 39 resident individuals that were detected for more than 30 days. There was no relationship with fish size and movement or site fidelity. Average home range (95% KUD) for residents was 8.5±0.5 km² compared to average sanctuary zone size of 30 km². Calculated home range was stable over time resulting in resident animals tagged inside the sanctuary zone spending ∼80% of time within the sanctuary boundaries. The number of fish remaining within the array of receivers declined steadily over time and after one year more than 60% of tagged fish had moved outside the sanctuary zone and also beyond the 28 km² array of receivers. Long term monitoring identified the importance of shifting home range and was essential for understanding overall residency within protected areas and also for identifying spawning related movements. This study indicates that despite exhibiting stable and small home ranges over periods of one to two years, more than half the population of spangled emperor move at scales greater than average sanctuary size within the Ningaloo Reef Marine Park.     

Differential Range Use between Age Classes of Southern African Bearded Vultures Gypaetus barbatus

Bearded Vulture Gypaetus barbatus movements were investigated in southern Africa to determine whether an individual''s age, sex or breeding status influenced its ranging behaviour and to provide the information required to guide conservation activities. Data from satellite transmitters fitted to 18 individuals of four age classes were used to determine range size and use. Because of the nature of the movements of marked individuals, these data could be used to determine the overall foraging range of the entire population, which was estimated to be 51 767 km². Although juvenile, immature and sub-adult birds used different parts of the overall range, their combined foraging range was 65% (33 636 km²) of the overall range. Average adult home ranges (286 km²) were only around 1% the size of the average foraging ranges of non-adults (10 540 –25 985 km²), with those of breeding adults being even smaller (95 km²). Home ranges of breeding adults did not vary in size between seasons but adults utilized their home range more intensively whilst breeding, moving greater distances during the incubation and chick hatching period. Range size and use increased as non-adults aged. Immatures and sub-adults had larger range sizes during winter, but range use of non-adults did not vary seasonally. Range size and use did not differ between the sexes in any of the age classes. Information on home range size and use enables specific areas within the species'' range to be targeted for management planning, education and conservation action.     

Interactions between density,home range behaviors,and contact rates in the Channel Island fox (Urocyon littoralis)

Many of the mechanisms underlying density‐dependent regulation of populations, including contest competition and disease spread, depend on contact among neighboring animals. Understanding how variation in population density influences the frequency of contact among neighboring animals is therefore an important aspect to understanding the mechanisms underlying, and ecological consequences of, density‐dependent regulation. However, contact rates are difficult to measure in the field and may be influenced by density through multiple pathways. This study explored how local density affects contact rates among Channel Island foxes (Urocyon littoralis) through two pathways: changes in home range size and changes in home range overlap. We tracked 40 radio‐collared foxes at four sites on San Clemente Island, California. Fox densities at the four sites ranged from 2.8 ± 1.28 to 42.8 ± 9.43 foxes/km². Higher fox densities were correlated with smaller home ranges (R² = 0.526, F_1,38 = 42.19, P < 0.001). Thirty foxes wore collars that also contained proximity loggers, which recorded the time and duration of occasions when collared foxes were within 5 m of one another. Contact rates between neighboring fox dyads were positively correlated with home range overlap (R² = 0.341, P = 0.008), but not fox density (R² = 0.012, P = 0.976). Individuals at high densities had more collared neighbors with overlapping home ranges (R² = 0.123, P = 0.026) but not an increase in the amount of contact between individual neighbors. This study was the first time contact rates were directly measured and compared to density and home range overlap. Results suggest that foxes exhibit a threshold in their degree of tolerance for neighbors, overlap is a reliable index of the amount of direct contact between island foxes, and disease transmission rates will likely scale with fox density.     

Seasonal home ranges and fidelity to breeding sites among ringed seals

Population structure and patterns of habitat use among ringed seals (Phoca hispida) are poorly known, in part because seasonal movements have not been adequately documented. We monitored the movements of 98 ringed seals in the Beaufort and Chukchi seas between 1990 and 2006 using three forms of telemetry. In the winter—spring period (when the seals were occupying shorefast ice), we used radio and ultra-sonic tags to track movements above and below the ice, respectively. We used satellite-linked transmitters in summer and fall (when the seals ranged away from their winter sites) to track at-sea movements. In the shorefast ice habitat, the home ranges of 27 adult males ranged from <1 to 13.9 km² (median = 0.628) while the home ranges of 28 adult females ranged from <1 to 27.9 km² (median = 0.652). The 3-dimensional volumes used by 9 seals tracked acoustically under the ice averaged 0.07 (SD = 0.04) km³ for subadults and adult males and 0.13 (SD = 0.04) km³ for adult females. Three of the radio-tracked seals and 9 tracked by satellite ranged up to 1,800 km from their winter/spring home ranges in summer but returned to the same small (1–2 km²) sites during the ice-bound months in the following year. The restricted movements of ringed seals during the ice-bound season—including the breeding season—limits their foraging activities for most of the year and may minimize gene flow within the species.     

Spatial ecology of wolverines at the southern periphery of distribution

Wolverines (Gulo gulo) in the conterminous United States have experienced range contraction, are uncommon, and have been designated as warranted for protection under the United States Endangered Species Act. Data from the southern edge of the wolverine's circumpolar distribution is sparse, and development of effective conservation strategies would benefit from a more complete understanding of the species' ecology. We captured and radio-monitored 30 wolverines in the Greater Yellowstone Ecosystem (GYE), tested for seasonal habitat selection by elevation band, and examined a suite of spatial characteristics to clarify our understanding of the wolverine's niche. Wolverines in GYE selected for areas >2,600 m latitude-adjusted elevation (LAE; n = 2,257 wolverine locations [12 F, 6 M]). Wolverines avoided areas <2,150 m LAE, including during winter when the vast majority of ungulates are pushed to these elevations by deep snow. Wolverine home ranges were large relative to body size, averaging 303 km² for adult females and 797 km² for adult males (n = 13 [8 F, 5 M] and 33 wolverine-years). Resident adults fit with Global Positioning System (GPS) collars used an area >75% the size of their multi-year home range in an average of 32 days (n = 7 [5 F, 2 M]). Average movement rates of 1.3 km/2-hr indicated that both sexes move distances equivalent to the diameter of their home range every 2 days or the circumference of their home range in <1 week (n = 1,329 2-hr movements, n = 12 individuals [7 F, 5 M]). This capability for movement, the short time-frame over which home ranges were developed, and a lack of home range overlap by same sex adults ( , 90% CI = 0.0–4.8%, n = 22 pairs) suggested territoriality. We estimated wolverine density to be 3.5/1,000 km² of area >2,150 m LAE (95% CI = 2.8–9.6). Dispersal movements extended to at least 170 km for both sexes (n = 5 F, 2 M). At the southern edge of distribution, where suitable and unsuitable conditions exist in close proximity, wolverines selected high-elevation areas near alpine tree-line where a mix of forest, meadow, and boulder fields were present, deep snow-cover existed during winter, and low temperatures near freezing can occur throughout the year. Persistence in these areas where the growing season is brief requires large home ranges that are regularly patrolled, a social system that provides exclusive access to resources, and low densities. These characteristics, along with low reproductive rates, are prevalent throughout the species range, indicating that wolverines are specialists at exploiting a cold, unproductive niche where interspecific competition is limited. The vulnerability inherent in occupying this unproductive niche was likely influential in previous declines within the conterminous United States and will remain a factor as wolverines encounter modern human influences. Conserving wolverines in the conterminous United States will require collaborative management over a large geographic scale. © 2011 The Wildlife Society.     

Resource partitioning among cape foxes,bat-eared foxes,and black-backed jackals in South Africa

Cape foxes (Vulpes chama) and bat-eared foxes (Otocyon megalotis) are sympatric with black-backed jackals (Canis mesomelas) over much of southern Africa, although competition with and/or predation by jackals may suppress local populations of both fox species. From 2005 to 2008, we captured, radio-collared, and monitored 11 cape foxes, 22 bat-eared foxes, and 15 black-backed jackals on a game ranch in South Africa to investigate their spatial, habitat, temporal, and dietary resource overlap. Mean annual home-range sizes were 27.7 km² for cape foxes, 5.0 km² for bat-eared foxes, and 17.8 km² for jackal family groups. Home ranges overlapped completely between species, although core areas overlapped less (<45%), with cape foxes and jackals overlapping the least (12%). When active, cape foxes, but not bat-eared foxes, used core areas of jackal groups less than expected. Additionally, both fox species used jackal core areas less than expected for their den sites, suggesting areas outside jackal core areas were used as refuges by foxes. Strong levels of habitat partitioning were not apparent at the study site or home-range levels, although habitat selection for den sites differed between jackals and cape foxes. Jackals were the most diurnal across seasons, whereas cape foxes were the most nocturnal. Diets overlapped little (R₀ = 0.20–0.34) among the canid species, with bat-eared foxes overlapping the least with the others. Jackals killed at least 5 collared bat-eared foxes and 1 collared cape fox, indicating potential interference competition, probably for exclusive use of territorial space rather than over shared resources. We conclude that bat-eared foxes coexisted with jackals primarily by their dietary specialization and group living. Cape foxes coexisted with jackals by exhibiting high levels of spatial, habitat, temporal, and dietary partitioning. Surprisingly, the fox species exhibited positive associations with each other. Our results show the mechanisms that may allow jackals to suppress fox populations, yet also show how foxes, in turn, use different mechanisms to coexist with a dominant canid. © 2012 The Wildlife Society.     

Spatial Ecology of a Canada Lynx Population in Northern Maine

Abstract Canada lynx (Lynx canadensis) were listed as a federally threatened species in 14 states at the southern extent of their geographic range in March 2000, with Maine being the only state in the northeastern United States known to support a resident population. Relatively little information is known about the ecology of lynx living at the southern edge of their range, including range requirements, movements, and spatial organization. Basic knowledge of lynx ecology is needed for federal recovery planning efforts. Between 1999 and 2004, we trapped and radiocollared 43 lynx (21 M, 22 F) in northern Maine in an intensively managed and predominantly early successional forested landscape. We estimated diurnal annual and seasonal home-range size for male and female lynx using the 85% fixed-kernel home-range estimator. Annual home ranges of adult male lynx (x̄ = 53.6 km²) were more than twice the size of adult female home ranges (x̄ = 25.7 km²). Home ranges of adult females during snow periods (x̄ = 38.3 km²) were nearly 3 times larger than their snow-free-period ranges (x̄ = 14.3 km²), whereas, snow-free ranges of adult males (x̄ = 58.8 km²) were slightly larger than their snow-period ranges (x̄ = 45.2 km²). We observed a limited amount of home-range overlap among lynx of the same sex (F: x̄ = 17.2%; M: x̄ = 11.8%). Lynx of opposite sex showed more extensive overlap (x̄ = 24.3%). Most home-range shifts of resident lynx were typically not extensive. Based on territory mapping, we estimated a minimum lynx density of 9.2–13.0 lynx/100 km². We observed lynx spatial ecology and densities that were more similar to northern lynx populations when hares were abundant than to other southern lynx populations, suggesting that region-specific studies under varying habitat conditions and hare densities are needed to ensure realistic recovery goals and effective management of lynx at the southern extent of their range.     

Extensive Predator Space Use Can Limit the Efficacy of a Control Program

ABSTRACT Reduced to small isolated groups by anthropogenic habitat losses or habitat modifications, populations of many endangered species are sensitive to additive sources of mortality, such as predation. Predator control is often one of the first measures considered when predators threaten survival of a population. Unfortunately, predator ecology is often overlooked because relevant data are difficult to obtain. For example, the endangered Gaspésie caribou (Rangifer tarandus caribou) has benefited from 2 periods of predator control that targeted black bears (Ursus americanus) and coyotes (Canis latrans) in an attempt to reduce predation on caribou calves. Despite a high trapping effort, the number of predators removed has remained stable over time. To assess impact of predator movements on efficacy of a control program, we studied space use of 24 black bears and 16 coyotes over 3 years in and around the Gaspésie Conservation Park, Quebec, Canada, using Global Positioning System radiocollars. Annual home ranges of black bears averaged 260 km² and 10 individuals frequented area used by caribou. Annual home ranges of resident coyotes averaged 121 km², whereas dispersing coyotes covered >2,600 km². Coyotes were generally located at lower altitudes than caribou. However, because coyotes undertook long-distance excursions, they overlapped areas used by caribou. Simulations based on observed patterns showed that 314 bears and 102 coyotes potentially shared part of their home range with areas used by female caribou during the calving period. Despite low densities of both predator species, extensive movement and use of nonexclusive territories seem to allow predators to rapidly occupy removal areas, demonstrating the need for recurrent predator removals. Our results underscore the necessity of considering complementary and alternative solutions to predator control to assure long-term protection of endangered species.     

A division between foraging range and territory related to food distribution in the red fox

Spatial organization of the red fox (Vulpes vulpes schrencki) was investigated on the basis of seasonal food distribution in the Shiretoko National Park, Hokkaido from 1992 to 1994. Four periods were recorded pertaining to the distribution of 2 kinds of food resources: human food and spawning salmonid carcasses. The home range utilizations of radio-collared foxes were compared for the periods. In the periods when food was not spatially concentrated, resident foxes were territorial, showing exclusive distribution of home ranges between families, defense against intruding foxes at the edge of home ranges, and site specific dominance over intruding foxes. In contrast, during periods when food distribution was concentrated, home ranges overlapped. In the latter periods, foxes made round trips of up to 8 km from their territories to the localized concentration of food, the distance that foxes can travel within a day. This suggests that red foxes in this area have unique foraging ranges that include some seasonally available food outside their territories, and that these ranges depend on fluctuating food distribution caused by humans.