scholarly journals Home Ranges and Spatial Organization of Fishers, Martes pennanti, in Central British Columbia

2009 ◽  
Vol 123 (2) ◽  
pp. 126 ◽  
Author(s):  
Richard D. Weir ◽  
Alton S. Harestad ◽  
Fraser B. Corbould

We described the size and spatial arrangement of aggregate and seasonal home ranges for 17 radio-tagged resident Fishers (Martes pennanti) that were >1.5 years old in two areas of central British Columbia during 1990-1993 and 1996-2000. We estimated home range size for each Fisher from the 95% isopleth of the utilization distribution generated using a fixed kernel model with smoothing selected by least-squares cross-validation (95% FK). For comparison to previous studies, we also calculated the minimum convex polygon estimate of home range size (MCP) for each animal. The aggregate home ranges (95% FK) of female Fishers (mean = 37.9 km², SD = 18.5, range = 10.5 – 81.2, n = 11) were significantly smaller than those of males (mean = 161.3 km², SD = 100.0, range = 46.0 – 225.2, n = 3; P = 0.019). We observed minor overlap among 95% FK home ranges of Fishers of the same sex, but considerable overlap among home ranges of males and females. Home ranges (95% FK or MCP) that we observed in central British Columbia were larger than those reported elsewhere in North America, particularly for males. We suggest that the distribution of resources for Fishers may occur at lower gross densitiesin central British Columbia than in other portions of the Fisher’s range and that suitable habitat in which Fishers can establish home ranges is not found uniformly across the landscape.

2010 ◽  
Vol 32 (2) ◽  
pp. 183 ◽  
Author(s):  
Ross L. Goldingay ◽  
David J. Sharpe ◽  
Matt D. J. Dobson

The home-range area of animals may vary geographically and in response to habitat quality. We investigated the size of squirrel glider (Petaurus norfolcensis) home ranges near Brisbane, Queensland, and at Tea Gardens on the central coast of New South Wales. Habitat at both sites had been partially cleared and had been subjected to grazing for several decades. Twelve gliders were tracked over an average of 3.5 months in Brisbane. The fixed kernel (FK95%) home-range estimate averaged 4.6 ± 0.7 (s.e.) ha while the minimum convex polygon (MCP100%) averaged 6.7 ± 1.5 ha. Six gliders were tracked over 1 month at Tea Gardens. The FK95% home-range estimate averaged 14.8 ± 2.4 ha while the MCP100% averaged 13.3 ± 3.1 ha. The Tea Gardens values are derived from relatively short periods and are likely to underestimate the areas used. This study demonstrates that home-range size can vary substantially in the squirrel glider. This has implications for understanding how this species responds to variation in habitat quality and highlights the need for site-specific studies to inform aspects of management.


1996 ◽  
Vol 23 (6) ◽  
pp. 711 ◽  
Author(s):  
G Saunders ◽  
B Kay

The movements of a subalpine population of feral pigs were examined at Kosciusko National Park in southeastern New South Wales. Sufficient data were collected to estimate the home-range area of 20 pigs on the basis of 782 telemetry and trap locations. Mean (+/- s.d.) home-range size (minimum convex polygon method) for males (35.0 t 22.2 km*2) was significantly greater than that for females (1 1.1 +/- 5.2 km*2). Use of capture-recapture distances to estimate home-range size was considered inappropriate. A test for nomadism suggests that, although home ranges of pigs in this environment were larger than those reported for other pigs in Australia, the pigs were essentially sedentary. Management implications for this population are discussed.


1990 ◽  
Vol 68 (9) ◽  
pp. 2016-2020 ◽  
Author(s):  
Michael A. Bowers ◽  
David N. Welch ◽  
Timothy G. Carr

Capture–recapture techniques were used to study the spatial organization of a population of eastern chipmunks, Tamias striatus, over 16 weeks of an uncharacteristically dry summer and early fall. The objective was to examine the role of free water as a factor influencing home range size. Home range size was estimated for time periods of 1, 3, and 5 weeks. For animals captured more than two times, home range size estimates were not significantly correlated with the number of captures or body weight, nor did home ranges differ between males and females. Home ranges were relatively large in early summer, small in mid- to late-summer, and large again in the early fall. Home ranges were significantly smaller during the 8 weeks of greater-than-median precipitation than during weeks of less-than-median precipitation. Home ranges of 8 individuals out of 12 increased in size during a 3-week drought period relative to their pre- and post-drought home ranges. Differences in home range size between drought and nondrought periods were more pronounced for males than females. Comparison of home range size before and after the provision of supplemental drinking water showed that where water was added, chipmunks reduced the size of their home ranges significantly more than control (unwatered) chipmunks. These results identity water availability during certain years and seasons as a factor influencing home range size.


1989 ◽  
Vol 67 (1) ◽  
pp. 178-181 ◽  
Author(s):  
Carol Haspel ◽  
Robert E. Calhoon

Home range size is stable among free-ranging cats in Brooklyn, New York. Marked male and female cats had mean home ranges of 2.6 (95% CI, 2.38–2.87) and 1.7 ha (95% CI, 1.57–1.98), respectively, as estimated by the population utilization distribution. Males had significantly larger home ranges, used the perimeter of their ranges more, and had greater variability in home range size than females. Gender differences in body weight accounted for observed differences in home range size; the seeking of estrous females by males could not account for differences in male and female home ranges. The availability of garbage or abandoned buildings, neighborhood, season, or experimental supplementary feeding did not influence home range size.


2006 ◽  
Vol 33 (5) ◽  
pp. 397 ◽  
Author(s):  
Ronald S. C. Firth ◽  
John C. Z. Woinarski ◽  
Richard A. Noske

Radio-telemetry was used to investigate the home range and den characteristics of the brush-tailed rabbit-rat (Conilurus penicillatus) from three sites in the monsoonal tropics of the Northern Territory, Australia. Radio-tracking was conducted in a series of discontinuous 4–17-day sessions, over a 2-year period. The home ranges of 61 C. penicillatus were estimated using the minimum convex polygon (MCP) and fixed kernel (K95% and K50%) methods. There were no significant differences in home-range size among the three sites or between wet and dry seasons, which suggests that vegetation structure, floristics and season play relatively little role in movements of C. penicillatus. The mean home-range size was 0.79 ± 0.09 ha (MCP estimate) to 0.97 ± 0.12 ha (K95% estimate). The home ranges of males were larger than those of females (mean MCP estimates of 1.07 ± 0.15 and 0.45 ± 0.06 ha respectively). C. penicillatus denned primarily in fallen logs and in hollows of eucalypts and bloodwoods (Corymbia spp.). Rough-barked trees appeared to be preferred. The diameter at breast height (DBH) of den trees varied significantly between the three sites, being greatest at site C1 (34.5 ± 2.4 cm) and least at site C2 (26.1 ± 1.0 cm). Den trees had larger DBH than randomly selected trees at each site. The diameter at the mid-point (DMP) of both den and randomly selected logs were not significantly different between sites. Many individuals used more than one den site per tracking session. The small home ranges of C. penicillatus and its reliance on hollows in trees and logs suggest that this species is very vulnerable to local extinction following long-term annual and destructive fire regimes and land clearing, even in comparatively small patches.


1993 ◽  
Vol 20 (5) ◽  
pp. 571 ◽  
Author(s):  
S Troy ◽  
G Coulson

Home range in the swamp wallaby, Wallabia bicolor (Marsupialia : Macropodoidea) was examined using radio-tracking in a 150-ha remnant of mixed eucalypt forest at Healesville, Victoria. Three methods were used to calculate home-range size: minimum convex polygons, fourier transform MAP(O.95) and MAP(0.50) estimation, and harmonic mean 50% isopleths and 95% isopleths. The minimum convex polygon method produced the largest estimate of home-range area (16.01 +/-.45 ha). Each method required a different number of fixes before home-range area estimates reached an asymptote. These data showed that W. bicolor have small, overlapping home ranges and that the shape of the home range varied between individuals. Home-range area was larger than previously reported for this species, and there was no significant difference between the sexes in home-range size.


1995 ◽  
Vol 43 (1) ◽  
pp. 91 ◽  
Author(s):  
JL Gardner ◽  
M Serena

Home-range size and overlap and movement patterns of adult male platypus, Ornithorhynchus anatinus, occupying streams in southern Victoria were investigated near the start of the breeding season using radio-tracking techniques. On the basis of a sample of males monitored for four or more complete activity periods, home-range size varied from 2.9 to 7.0 km, with individuals (n = 4) moving a mean net distance of 2.0 +/- 1.4 km per activity period. Longer-range movements were also observed, with one male travelling at least 15 km from one stream catchment to another via an intervening stretch of river. Some home ranges of males were mutually exclusive whereas others overlapped substantially; in the latter case, males largely avoided each other, spending most of their time in different parts of the shared area. All home ranges of males apparently overlapped those of two or more adult females. Three patterns of travel over complete activity periods were recognised, including unidirectional travel (point A to B), return travel (A to B to A) and multidirectional travel with multiple, relatively short-range backtracking. Males occupying overlapping areas often moved multidirectionally and rarely undertook unidirectional travel, whereas the converse applied to males occupying exclusive areas.


Author(s):  
M.G.L. Mills ◽  
M.E.J. Mills

Home ranges of males (1204 km2) and females (1510 km2) were similar. Female home range size was positively related to the dispersion of prey and generally, but not exclusively, they displayed home range fidelity. Overlap between female home ranges was extensive, although they rarely met up. Male home ranges overlapped extensively and there was no difference in size between coalition and single males. Males overcame the problem of scent marking a large home range by concentrating scent marks in core areas. Generally female cheetah home range size is affected by resource productivity, although where prey are migratory, or in fenced reserves where movements are constricted, and areas where disturbance is severe, this may be different. Southern Kalahari males apparently need large home ranges to increase the likelihood of locating wide-ranging and sporadically receptive females. Mean dispersal distance for subadult males (96 km) was further than for females (39 km).


2018 ◽  
Vol 96 (6) ◽  
pp. 545-552 ◽  
Author(s):  
Alexander M. Chang ◽  
Karen L. Wiebe

Meeting energy requirements during the nonbreeding season is important for many animals and some defend winter territories to secure a food supply. In birds of prey, females, the larger and competitively dominant sex, may monopolize areas with higher prey abundance than males. We thus predicted that female Snowy Owls (Bubo scandiacus (Linnaeus, 1758)), which might acquire the high-quality habitats and individuals in better body condition, would be able to persist on smaller home ranges, travel shorter distances, and spend proportionally more time on a home range than males, during the winter. On the prairies in central Saskatchewan, we deployed satellite transmitters on 11 male and 12 female Snowy Owls over two winters. There were no significant differences between the sexes in home-range size or the amount of travelling during the winter months. Mean first home range (95% minimum convex polygon) size was 54.4 km2 for males, 31.9 km2 (estimated marginal means) for females, and 53.8 km2 for the sexes combined. However, within sexes, home-range size was negatively correlated with body condition as predicted. A lack of defense of home-range perimeters against conspecifics could increase variation in home-range size and movement patterns and reduce differences between the sexes.


2014 ◽  
Vol 2014 ◽  
pp. 1-14 ◽  
Author(s):  
Nicholas A. Farmer ◽  
Jerald S. Ault

Underestimation of reef fish space use may result in marine reserves that are too small to effectively buffer a portion of the stock from fishing mortality. Commonly used statistical home range models, such as minimum convex polygon (MCP) or 95% kernel density (95% KD) methods, require the exclusion of individuals who move beyond the bounds of the tracking study. Spatially explicit individual-based models of fish home range movements parameterized from multiple years of acoustic tracking data were developed for three exploited coral reef fishes (red grouperEpinephelus morio, black grouperMycteroperca bonaci, and mutton snapperLutjanus analis) in Dry Tortugas, Florida. Movements were characterized as a combination of probability of movement, distance moved, and turning angle. Simulations suggested that the limited temporal and geographic scope of most movement studies may underestimate home range size, especially for fish with home range centers near the edges of the array. Simulations provided useful upper bounds for home range size (red grouper:2.28±0.81 km2MCP,3.60±0.89 km2KD; black grouper:2.06±0.84 km2MCP,3.93±1.22 km2KD; mutton snapper:7.72±2.23 km2MCP,6.16±1.11 km2KD). Simulations also suggested that MCP home ranges are more robust to artifacts of passive array acoustic detection patterns than 95% KD methods.


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