Home ranges and movements of red foxes in central Europe: stability despite environmental changes

1995 ◽  
Vol 73 (10) ◽  
pp. 1960-1966 ◽  
Author(s):  
Jean-Steve Meia ◽  
Jean-Marc Weber
Keyword(s):  
Home Range ◽  
Snow Cover ◽  
Central Europe ◽  
Rural Areas ◽  
Environmental Changes ◽  
Home Range Size ◽  
Territory Size ◽  
Home Ranges ◽  
Red Foxes ◽  
The Individual

Thirteen red foxes (Vulpes vulpes) were radio-tracked between September 1989 and August 1993 in the Swiss Jura mountains. Home ranges of subadult and adult resident foxes did not differ and were small (seasonal estimates 0.48–3.06 km2). A nomadic adult was also monitored; it used a significantly larger area (12.71–25.90 km2). In most cases, home range sizes did not vary seasonally and were not affected by drastic changes in food availability. That foxes maintain a constant territory size is in accordance with both the "contractor" and "obstinate" strategies. The small observed sizes suggest that after the eradication of rabies, rural areas of central Europe are very good habitats for foxes. In the absence of clumped feeding patches or constraining factors (e.g., deep snow cover), the foxes moved regularly throughout their home range, typically in a "non-oriented zigzag." The distance travelled per day seemed to be affected only by home range size (positive correlation) and occasionally, according to the individual, by weather or snow cover. On average, the foxes moved 3.9–12.0 km a day. Despite its significantly larger home range, the nomadic fox did not move more than the resident foxes; the physical characteristics of red foxes probably set a limit to the distance travelled daily.

Allometry of home range size in lake and river fishes

1995 ◽  
Vol 52 (7) ◽  
pp. 1499-1508 ◽  
Author(s):  
Charles K. Minns
Keyword(s):  
Body Size ◽  
Home Range ◽  
Freshwater Fish ◽  
Fish Population ◽  
Home Range Size ◽  
Range Size ◽  
Territory Size ◽  
Home Ranges ◽  
Data Set ◽  
Terrestrial Mammals

A data set assembled from published literature supported the hypotheses that (i) home range size increases allometrically with body size in temperate freshwater fishes, and (ii) fish home ranges are larger in lakes than rivers. The allometric model fitted was home range = A∙(body size)B. Home ranges in lakes were 19–23 times larger than those in rivers. Additional analyses showed that membership in different taxonomic groupings of fish, the presence–absence of piscivory, the method of measuring home range, and the latitude position of the water bodies were not significant predictive factors. Home ranges of freshwater fish were smaller than those of terrestrial mammals, birds, and lizards. Home ranges were larger than area per fish values derived by inverting fish population and assemblage density–size relationships from lakes and rivers and territory–size relationships in stream salmonids. The weight exponent (B) of fish home range was lower than values reported for other vertebrates, 0.58 versus a range of 0.96–1.14. Lake–river home range differences were consistent with differences reported in allometric models of freshwater fish density and production.

Social Structure and Patterns of Movement of the Western Pebble-mound Mouse, Pseudomys chapmani, at Marandoo, Western Australia

1997 ◽  
Vol 24 (3) ◽  
pp. 295 ◽  
Author(s):  
S. D. Anstee ◽  
J. D. Roberts ◽  
J. E. O'Shea
Keyword(s):  
Home Range ◽  
Home Range Size ◽  
Ore Deposits ◽  
Core Area ◽  
Home Ranges ◽  
Economic Significance ◽  
Iron Ore Deposits ◽  
The Individual ◽  
High Level ◽  
The Impact

Mounds of the western pebble-mound mouse, Pseudomys chapmani, are found throughout the species’ Pilbara range in areas with iron-ore deposits of economic significance. Translocation techniques are being examined as a means of minimising the impact of mining on this species. In the absence of detailed information on the biology of Pseudomys chapmani, translocation is inadvisable. To provide such basic information, animal densities, mound demographics and population sizes, and home-range and core-area sizes were obtained by a combination of trapping and radio-tracking. Mounds of Pseudomys chapmani were found to be inhabited by social groups of up to 12 animals. Estimates of home-range size gave mean ( s.e.) values of 14·4 6·7 ha and 4·6 2·7 ha for males and females, respectively; core areas were recorded at 0·93 0·29 ha for males and 0·29 0·16 ha for females. Considerable overlap of home ranges was recorded between individuals from the same and different mounds. Overlap at the core-area level occurred only between individuals from the same mound. The high level of social complexity and mound fidelity indicates that translocations should be directed at the level of the social group rather than at the level of the individual.

scholarly journals Factors Affecting Home Ranges of Red Foxes in Ikh Nart Nature Reserve, Mongolia

2012 ◽  
Vol 10 (1-2) ◽  
pp. 51-58
Author(s):  
Tserendorj Munkhzul ◽  
◽  
Bayarbaatar Buuveibaatar ◽  
James D. Murdoch ◽  
Richard P. Reading ◽  
...  
Keyword(s):  
Home Range ◽  
Nature Reserve ◽  
Radio Telemetry ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Red Foxes ◽  
Factors Affecting ◽  
Intrinsic Factors ◽  
Range Dynamics

Changes in red fox home range size in relation to environmental and intrinsic factors were studied using radio-telemetry during 2006–2008 in Ikh Nart Nature Reserve, southeastern Mongolia. We captured a total of 12 red foxes (8 females and 4 males) and fi tted them with VHF radio-collars. Marked animals were tracked up to fi ve times a week to estimate home ranges. We also trapped small mammal and insects in different biotopes for 3 years to estimate relative abundance of prey. Our results showed that mean individual home range sizes varied widely and differed among years. There was variation in home ranges between adults versus juveniles, but no signifi cant difference was found between males versus females. In addition, mean home range size did not differ seasonally for pooled years. Variation in home ranges was best explained by a model that included covariates of year and age. We suggest that spatiotemporal changes in resource availability across years infl uenced home range dynamics of red foxes in our study.

Summer home range and habitat utilisation of the red fox (Vulpes vulpes) in a tundra habitat, northwest British Columbia

1982 ◽  
Vol 60 (5) ◽  
pp. 807-812 ◽  
Author(s):  
Donald M. Jones ◽  
John B. Theberge
Keyword(s):  
British Columbia ◽  
Home Range ◽  
Small Mammals ◽  
Vulpes Vulpes ◽  
Home Range Size ◽  
Ground Squirrels ◽  
Home Ranges ◽  
Red Foxes ◽  
Spermophilus Parryii ◽  
Arctic Ground Squirrels

Eight adult red foxes (Vulpes vulpes) were radio tracked during the summers of 1978 and 1979 in an alpine and subalpine environment of northwest British Columbia. The spatial distributions of small mammals (mice, voles, and shrews) and arctic ground squirrels (Spermophilus parryii) were ascertained to complement the telemetric study. Summer home ranges averaged 1611 ha (range = 277–3420 ha) and were larger than vulpine ranges in temperate environments. Significant habitat selection was evident in five of the seven home ranges that were examined. Salix shrub communities were preferred habitats, whereas, open lichen – Empetrum and fen communities were avoided. Relative densities of small mammals and arctic ground squirrels varied significantly among plant communities. Possible explanations, considering the diet of the fox and the spatial distribution of its prey, are offered to account for the observed patterns of home-range size and habitat utilisation.

Home Range, Dispersal and Density of Red Foxes (Vulpes Vulpes L.) In Central Victoria.

1991 ◽  
Vol 18 (2) ◽  
pp. 215 ◽  
Author(s):  
BJ Coman ◽  
J Robinson ◽  
C Beaumont
Keyword(s):  
Home Range ◽  
Radio Telemetry ◽  
Control Program ◽  
Total Sample ◽  
Home Range Size ◽  
Dispersal Distance ◽  
Breeding Pair ◽  
Home Ranges ◽  
Red Foxes ◽  
Central Victoria

Between 1983 and 1986, various aspects of red fox spatial behaviour were studied in both rural and semi-urban environments in central Victoria. Using radio-telemetry, the short-term home ranges of three adult foxes (2 male, 1 female) in a pasture/woodland habitat were estimated to be of the order of 5-7 km2 each. In a semi-urban environment nearby, the home ranges of a further 3 adult animals (2 male, 1 female) were estimated to be 0.6-1.3 km2 each. Estimates of home range size based on a 90% space utilisation effectively halved the home range area for all six foxes. There were indications that, for the animals concerned, ranges were mutually exclusive except in the case of a breeding pair which shared a common home range. During the studies, 137 young fox cubs were ear-tagged and released at the point of capture. Subsequently, 46 of these animals were returned by hunters. Nearly 70% of the returned animals were killed at a distance of 2 km or less from the tagging site but dispersal distances of up to 30 km were recorded. The average dispersal distance for animals killed more than 2 km from the tagging site was 11 km. Estimates of fox density in a rural area of some 2400 ha were obtained by a survey of active breeding dens in the 1985 and 1986 breeding seasons. Assuming one breeding pair plus three surviving young per litter, the maximum summer density was estimated at about 3.0 foxes km-2 and the minimum winter density as about 1.2 foxes km-2. For a further estimate of density, 13 foxes were live-captured, fitted with radios and released. In a short control program on the study area a few weeks later, 7 of these animals were recovered in a total sample of 50 foxes killed. The remaining 6 foxes were established as still present in the study area. Using this capturehecapture data, an early autumn density of about 3.9 foxes km-2 was indicated. The significance of this data in relation to the possible role of foxes as vectors of rabies disease in Australia is discussed.

Movement patterns of feral predators in an arid environment – implications for control through poison baiting

2009 ◽  
Vol 36 (5) ◽  
pp. 422 ◽  
Author(s):  
K. E. Moseby ◽  
J. Stott ◽  
H. Crisp
Keyword(s):  
Home Range ◽  
Sand Dunes ◽  
Activity Patterns ◽  
Movement Patterns ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Feral Cats ◽  
Poison Baiting ◽  
Specific Variation

Control of introduced predators is critical to both protection and successful reintroduction of threatened prey species. Efficiency of control is improved if it takes into account habitat use, home range and the activity patterns of the predator. These characteristics were studied in feral cats (Felis catus) and red foxes (Vulpes vulpes) in arid South Australia, and results are used to suggest improvements in control methods. In addition, mortality and movement patterns of cats before and after a poison-baiting event were compared. Thirteen cats and four foxes were successfully fitted with GPS data-logger radio-collars and tracked 4-hourly for several months. High intra-specific variation in cat home-range size was recorded, with 95% minimum convex polygon (MCP) home ranges varying from 0.5 km2 to 132 km2. Cat home-range size was not significantly different from that of foxes, nor was there a significant difference related to sex or age. Cats preferred habitat types that support thicker vegetation cover, including creeklines and sand dunes, whereas foxes preferred sand dunes. Cats used temporary focal points (areas used intensively over short time periods and then vacated) for periods of up to 2 weeks and continually moved throughout their home range. Aerial baiting at a density of 10 baits per km2 was ineffective for cats because similar high mortality rates were recorded for cats in both baited and unbaited areas. Mortality was highest in young male cats. Long-range movements of up to 45 km in 2 days were recorded in male feral cats and movement into the baited zone occurred within 2 days of baiting. Movement patterns of radio-collared animals and inferred bait detection distances were used to suggest optimum baiting densities of ~30 baits per km2 for feral cats and 5 per km2 for foxes. Feral cats exhibited much higher intra-specific variation in activity patterns and home-range size than did foxes, rendering them a potentially difficult species to control by a single method. Control of cats and foxes in arid Australia should target habitats with thick vegetation cover and aerial baiting should ideally occur over areas of several thousand square kilometres because of large home ranges and long-range movements increasing the chance of fast reinvasion. The use of temporary focal points suggested that it may take several days or even weeks for a cat to encounter a fixed trap site within their home range, whereas foxes should encounter them more quickly as they move further each day although they have a similar home-range size. Because of high intra-specific variability in activity patterns and home-range size, control of feral cats in inland Australia may be best achieved through a combination of control techniques.

Ecological Correlates of Fecal Corticosterone Metabolites in Female Greater Sage-Grouse (Centrococercus urophasianus)

2021 ◽  
Author(s):  
Jordan Clark Rabon ◽  
Cassandra M. V. Nuñez ◽  
Peter Coates ◽  
Mark Ricca ◽  
Tracey N. Johnson
Keyword(s):  
Home Range ◽  
Stress Responses ◽  
Habitat Degradation ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Remotely Sensed Data ◽  
Sage Grouse ◽  
Ecological Conditions ◽  
Annual Grasses

Measurement of physiological responses can reveal effects of ecological conditions on an animal and correlate with demographic parameters. Ecological conditions for many animal species have deteriorated as a function of invasive plants and habitat fragmentation. Expansion of juniper (Juniperus spp.) trees and invasion of annual grasses into sagebrush (Artemisia spp.) ecosystems have contributed to habitat degradation for Greater Sage-Grouse (Centrococercus urophasianus (Bonaparte, 1827); hereafter, “Sage-Grouse”), a species of conservation concern throughout its range. We evaluated relationships between habitat use in a landscape modified by juniper expansion and annual grasses and corticosterone metabolite levels (stress responses) in feces (FCORTm) of female Sage-Grouse. We used remotely sensed data to estimate vegetation cover within hens’ home ranges and accounted for factors that influence FCORTm in other vertebrates, such as age and weather. We collected 36 fecal samples from 22 radio-collared hens during the brood-rearing season (24 May–26 July) in southwestern Idaho 2017–18. Concentrations of corticosterone increased with home range size but decreased with reproductive effort and temperature. The importance of home range size suggests that maintaining or improving habitats that promote smaller home ranges would likely facilitate a lower stress response by hens, which should benefit Sage-Grouse survival and reproduction.

scholarly journals Home Ranges and Movements of Elk (Cervus canadensis) Restored to Southern Ontario, Canada

2017 ◽  
Vol 130 (4) ◽  
pp. 320 ◽  
Author(s):  
Rick Rosatte
Keyword(s):  
Home Range ◽  
Home Range Size ◽  
Home Ranges ◽  
Winter Range ◽  
The Social ◽  
Cervus Canadensis ◽  
Summer Range ◽  
Seasonal Basis ◽  
Social Units ◽  
Winter Feeding

During 2000 and 2001, Elk (Cervus canadensis) were restored to the Bancroft, Ontario area. The objective of this study was to determine the home range and movements of six social units of Elk, 5–12 years after restoration, in an area of about 2500 km2 near Bancroft. Home range and movements were calculated from 40 221 Global Positioning System locations acquired from 56 collared Elk (16 bulls and 40 cows) between 2006 and 2013. Annual home ranges were found to be significantly greater (mean 110.3 km2, standard error [SE] 11.2) for Elk in areas where winter feeding by humans did not occur compared with those (mean 51.0 km2, SE 9.0) where winter feeding was prevalent. Elk in winter feeding areas had smaller ranges in winter than other seasons. On a seasonal basis, home range size was larger for Elk in areas where winter feeding did not occur; mean winter home range for Elk in non-feeding areas was 73.4 km2 (SE34.0) compared with 8.3 km2 (SE 2.6) for Elk in areas where winter feeding occurred. The 20 Elk that were monitored for multiple years exhibited home range fidelity among years. The entire range of all radio-collared Elk within the social groups studied covered 1716.4 km2 during 2006–2013. Average daily movements of Elk in the study arearanged from 1.0 to 2.1 km/day with greatest movements occurring during spring and summer. However, some Elk were capable of moving an average of 5–7km in a 12-h interval. Movements (about 5 km) to winter range occurred during October to December each year. Cows moved to calving areas in May with mean movements of Elk to spring/summer range about 6 km. Cow/calf groups moved to fall ranges by early September with mean movements of about 4 km. During the rut, mean bull movements of 16.0 km to cow groups over 1–5 days occurred in early September. Hunting of Elk during the fall of 2011 and 2012 did not appear to significantly affect the movements and dispersion of Elk in the study area.

Influence of habitat on home-range size in the short-beaked echidna

2012 ◽  
Vol 60 (1) ◽  
pp. 46 ◽  
Author(s):  
Jenny Sprent ◽  
Stewart C. Nicol
Keyword(s):  
Home Range ◽  
Spatial Ecology ◽  
Habitat Type ◽  
Negative Relationship ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Location Data ◽  
Significant Negative Relationship ◽  
Solitary Species

The size of an animal’s home range is strongly influenced by the resources available within it. In productive, resource-rich habitats sufficient resources are obtainable within a smaller area, and for many species, home ranges are smaller in resource-rich habitats than in habitats with lower resource abundance. Location data on 14 male and 27 female echidnas (Tachyglossus aculeatus) fitted with tracking transmitters, in the southern midlands of Tasmania, were used to test the influence of habitat type on home-range size. We hypothesised that as woodland should offer more shelter, food resources and refuges than pasture, echidnas living in woodland would have smaller home ranges than those living in pasture areas. We found significant differences between the sexes. Male echidnas had a significantly larger mean home range than females and a quite different relationship between home-range size and habitat type from females. There was no relationship between the proportion of woodland within male home ranges and home-range size whereas female echidnas had a highly significant negative relationship. This suggests that home-range size of female echidnas is highly influenced by the amount of woodland within it, but the home-range size of male echidnas is controlled by factors other than habitat. This pattern is consistent with the spatial ecology of many other solitary species with a promiscuous mating system. The home ranges of females are scaled to encompass all necessary resources for successfully raising their young within a minimal area, whilst the large home ranges of males are scaled to maximise access to females.

Snowmobile Effects on Movements of White-tailed Deer: A Case-study

1979 ◽  
Vol 6 (1) ◽  
pp. 45-51 ◽  
Author(s):  
Ronald G. Eckstein ◽  
Thomas F. O'Brien ◽  
Orrin J. Rongstad ◽  
John G. Bollinger
Keyword(s):  
Home Range ◽  
Habitat Use ◽  
Odocoileus Virginianus ◽  
Activity Patterns ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges

The effects of snowmobile traffic on the winter home-ranges, movements, and activity patterns, of White-tailed Deer (Odocoileus virginianus), were studied during two winters in northern Wisconsin. There were no significant differences in home-range size and habitat use of the Deer in areas with and without snowmobiling. However, snowmobiling caused some Deer to leave the immediate vicinity of the snowmobile trail. Deer were most affected when they were within 61 m of the snowmobile trail.

Sign in / Sign up

Export Citation Format

Share Document