Spatial Organisation of Urban Feral Cats (Felis Catus) in Jerusalem.

1995 ◽  
Vol 22 (3) ◽  
pp. 299 ◽  
Author(s):  
V Mirmovitch

Feral cats were studied for 10 months in a residential area in Jerusalem and their spatial distribution compared during two 1-month periods, the first in the autumn prior to the mating season and the second during the mating season (winter). Cat locations were recorded by direct observations, and home-range sizes were calculated with the minimum convex polygon method. No significant change in home-range size of adult males or females was found between the 2 periods. Young males expanded their home ranges considerably during their first mating season. Home ranges of males were significantly larger than those of females in both periods (0.56 and 0.30 ha, respectively, in autumn; 0.75 and 0.27 ha in winter). The home ranges of both sexes overlapped considerably with individuals of the same sex. Overlap among home ranges of females indicated a group pattern. High overlap (80%) was found among females that fed from the same set of garbage bins with similar frequency. Lower overlap (20%) was found between individual females that shared only a subset of their food resources and used it with different frequency. It is suggested that the distribution of food patches (garbage bins), the amount of food available and the rate of food renewal determined the cats' spatial organisation.

1991 ◽  
Vol 18 (6) ◽  
pp. 741 ◽  
Author(s):  
NPE Langham ◽  
RER Porter

The movements of a population of feral cats (Felis catus) were monitored on New Zealand farmland over three years by means of radiotelemetry. The number of resident males on the 5.2-km2 study area varied from 5 to 9, averaging 1.34 per km2, compared with 10-13 females, averaging 2.19 per km2. The average density over three years was 3.47 cats per km2. The nocturnal home range was significantly larger than the diurnal home range in both sexes. Adult female's home ranges overlapped considerably; adult males tended to occupy exclusive home ranges or territories with little overlap, but including those of several females. Adult males and females that used barns as den sites were mainly nocturnal and had larger home ranges than females denning in vegetation. Females showed no consistent change in home-range size with season, although those breeding in barns had larger home ranges in summer. Adult males had larger territories in summer and winter. Dispersing subadult males had a similar home range to adult males. Death or disappearance of a dominant male allcwed new males to occupy the vacated territory. Two subadults were tracked by day until they became adult and acquired territories within the study area.


2009 ◽  
Vol 36 (5) ◽  
pp. 422 ◽  
Author(s):  
K. E. Moseby ◽  
J. Stott ◽  
H. Crisp

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.


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.


2006 ◽  
Vol 84 (3) ◽  
pp. 404-411 ◽  
Author(s):  
A J Edelman ◽  
J L Koprowski

We compared home ranges of introduced Abert's squirrels (Sciurus aberti Woodhouse, 1853) in mixed-conifer forests of Arizona during non-mating and mating seasons. Because Abert's squirrels are reported to depend on ponderosa pine (Pinus ponderosa P. & C. Lawson) forests, the mixed-conifer forest in our study represented a novel habitat. Home-range size, home-range overlap with females, and movement distances increased for males from non-mating to mating seasons. Home-range size and overlap characteristics of females remained consistent between seasons, but movement distances were reduced during the mating season. Males probably increased home-range size, home-range overlap with females, and movement distances during the mating season to maximize contact with scarce females. Home-range size and overlap characteristics of female Abert's squirrels likely remained stable between seasons because females do not search for mates. Restricted movements by females during the mating season may be due to changes in resource use in preparation for reproduction. Non-mating season home ranges in our study were smaller than home ranges observed in ponderosa pine forest. Abert's squirrels in mixed-conifer forest may have small home ranges because resource quality is higher than in ponderosa pine forest or competition for space with co-occurring Mount Graham red squirrels (Tamiasciurus hudsonicus grahamensis (J.A. Allen, 1894)).


1992 ◽  
Vol 19 (6) ◽  
pp. 707 ◽  
Author(s):  
NPE Langham

The activity patterns of a resident population of 15 feral cats (Felis catus L.) on New Zealand farmland were investigated from March 1984 until February 1987 by radiotelemetry. Females could be divided into two separate groups: (1) those denning in barns and (2) those denning in the swamp and willows. Females denning in barns were mainly nocturnal except in spring and summer when rearing kittens. Barn cats moved significantly further between dusk and dawn, except in autumn-winter, than those denning in swamp and willows which were active over 24 h. When not breeding, related females occupied the same barn. In both groups, the home range of female relatives overlapped. Males ranged over all habitats, and dominant adult males moved significantly further and had larger home ranges than other males in all seasons, except in summer when they rested, avoiding hot summer days. Only adult males were active during the day in spring and autumn-winter. The importance of a Zeitgeber in synchronising cat activity with that of the prey is examined. The significance of female den site is discussed in relation to proximity of food, predators, social behaviour and male defence.


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.


2010 ◽  
Vol 124 (2) ◽  
pp. 139 ◽  
Author(s):  
F. Neil Dawson ◽  
Audrey J. Magoun ◽  
Jeff Bowman ◽  
Justina C. Ray

We conducted the first radio-telemetry study of Wolverines in northwestern Ontario during the winter of 2003-2004 to determine whether home ranges and movements of Wolverines in lowland boreal forest were typical of this species in other ecosystems and to describe reproductive den sites in this habitat type. Seven Wolverines (3 M, 4 F) were radio-tagged and monitored for 31 to 269 (Mean ± SE = 153 ± 35) days using a combination of remotely monitored Argos satellite and conventional aerial telemetry. Male and female 95% minimum convex polygon (MCP) home ranges (±SE) during December to October were 2,563 (796) km2 and 428 (118) km2, respectively, for combined VHF and Argos locations. A lactating female had a 95% MCP home range of 262 km2. The den site for this female included large boulders and downed trees, similar to dens described for this species in montane ecosystems. Boulder complexes and downed trees may be critical features of wolverine dens in lowland boreal forests. Mean road densities (± SE) within 95% MCP and 50% MCP home ranges were 0.43 (0.13) and 0.33 (0.23) km/km2, respectively, and our results suggest that road densities may affect selection of home ranges by Wolverines. The Wolverine population was a resident, reproductive population. Erratum for table included.


1999 ◽  
Vol 59 (1) ◽  
pp. 125-130 ◽  
Author(s):  
C. F. D. ROCHA

The home range of the Tropidurid lizard Liolaemus lutzae, an endemic species of the costal sand dune habitats of Rio de Janeiro State, was studied in the beach habitat of Barra de Maricá restinga, Maricá County. Home ranges were studied using a mark-recapture technique in a delimited area at the beach habitat. I considered for estimates and analysis the home ranges of those lizards with a minimum of four positions. The size of L. lutzae home ranges varied according to the segment of the population. The mean home range size of adult males (x = 59.8 ± 33.7 m²) was significantly larger than that of adult females (x = 22.3 ± 16.1 m²). Juvenile mean home range size was significantly smaller than that of adult males, but did not differ from that of adult females (t = 1.058; p = 0.149). The overlap between male home ranges was usually low (3.6%), being in general only peripheral. Conversely, there was a considerable overlap between home ranges of adult females with those of adult males, the home range areas of two or three females being enclosed in the home range of one adult male. The small overlap between home ranges of adult males suggested mutual exclusion. The observed between-sex differences in the size of L. lutzae home range may be explained by the sexual dimorphism in body size in this species, and by the need of adult males to establish larger areas so as to include many females in their areas, during the reproductive season. The differences in home range along ontogeny probably result from differences in body size of the different segments of the population, due to trophic differences (carnivory and herbivory levels), and the dispersal of young after birth. Because L. lutzae is omnivorous, but primarily herbivorous when adult, and due to its sit-and-wait foraging behavior (mainly on arthropods), it does not need to move around over large areas to find food, which in turn reduces the area necessary for it to live.


2005 ◽  
Vol 32 (1) ◽  
pp. 7 ◽  
Author(s):  
Andrew W. Claridge ◽  
David Paull ◽  
James Dawson ◽  
Greg Mifsud ◽  
Andy J. Murray ◽  
...  

The home ranges, movement patterns and spatial organisation of spotted-tailed quolls (Dasyurus maculatus maculatus) were studied in rainshadow woodland in southern New South Wales, Australia. Fourteen individuals were radio-collared and simultaneously tracked. Home-range size estimates ranged from 621 ha to at least 2561 ha for males, and 88 ha to at least 653 ha for females. Mean home-range size was significantly greater for males (992 ± 276 ha) than females (244 ± 72 ha). The maximum straight-line distances between successive fixes for males over 24-h and 48-h periods were 2529 and 4430 m, respectively, while for females these distances were 1865 and 3085 m. Mean maximum straight-line distances between successive fixes for males over a 24-h period were not significantly different from mean maximum straight-line distances of females (1493 ± 918 v. 1034 ± 540 m). However, over 48 h, the mean maximum distances between successive fixes for males was greater than that of females (2911 ± 934 v. 1680 ± 918 m). The home ranges of males mostly overlapped with those of other individuals, regardless of sex. In contrast, home ranges of females tended not to overlap with those of other females, suggesting some form of spatial separation. Home-range estimates derived for spotted-tailed quolls in our rainshadow woodland study site are comparable to those obtained for the species in wetter vegetation types. From a conservation perspective, it seems that habitat structure and the availability of prey is more important than rainfall or vegetation type in determining spatial requirements of the species. Until more advanced telemetry systems are developed, caution should be applied when using current home-range data on the species to infer breeding systems and patterns of spatial organisation, particularly the issue of territoriality among female quolls.


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.


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