Home range of stoats (Mustela erminea) in podocarp forest, south Westland, New Zealand: implications for a control strategy

2001 ◽  
Vol 28 (2) ◽  
pp. 165 ◽  
Author(s):  
Craig Miller ◽  
Mike Elliot ◽  
Nic Alterio

The home range of stoats (Mustela erminea) was determined as part of a programme to protect Okarito brown kiwi chicks (Apteryx australis) ‘Okarito’, from predation. Twenty-seven stoats were fitted with radio-transmitters and tracked in two podocarp (Podocarpaceae) forests, in south Westland, New Zealand, from July 1997 to May 1998. Home-range area was determined for 19 animals by minimum convex polygons and restricted-edge polygons, and core areas were determined by hierarchical cluster analysis. The mean home ranges of males across all seasons calculated by minimum convex polygon (210 28 ha ( s.e.)) and restricted-edge polygon (176 29 ha) were significantly larger than those of females across all seasons (89 14 ha and 82 12 ha). The mean home range of males calculated by minimum convex polygon during the breeding season (256 38 ha) was significantly larger than the mean home range pooled across the non-breeding seasons (149 16 ha), whereas that calculated by restricted-edge polygon was not significantly different. The mean home range of females during the breeding season was not significantly different from that in the non-breeding seasons when estimated by either method. Overlap of home ranges was observed within and between sexes in all seasons, with the greatest proportion of home range overlap being male–female. The mean home range of females in spring and summer is used to guide the spacing of control stations.

2004 ◽  
Vol 31 (3) ◽  
pp. 327 ◽  
Author(s):  
Helen Puckey ◽  
Milton Lewis ◽  
David Hooper ◽  
Carrie Michell

Radio-telemetry was used to examine the home range, movement and habitat utilisation of the critically endangered Carpentarian rock-rat (Zyzomys palatalis) in an isolated habitat patch in the Gulf of Carpentaria hinterland over a 13-month period. Two home-range estimators were used in the study, (i) minimum convex polygon (MCP) and (ii) fixed Kernel (KL), the latter also being used to estimate core areas of activity. Based on a total sample size of 21 individuals, the mean MCP home range was 11 165 m2, similar to the mean KL home range of 10 687 m2. Core areas were, on average, 11.9% of the KL home-range estimate. There was no significant difference in the size of home range or core area of males and females. Juveniles had a significantly smaller home range than adults. Home ranges and, to a lesser degree, core areas were non-exclusive, with multiple areas of overlap (averaging 41% and 38% respectively) within and between all age and gender categories, but especially between males and between juveniles. Movement frequencies showed that animals made many short forays in a central area close to the arithmetic home-range mean and far fewer long forays of distances greater than 100 m from the central area. The spatial and temporal activity of Z. palatalis was concentrated in, but not confined to, the 'valley' and 'slope' habitats, with fewer movements of rats onto the surrounding 'plateau'. Resource selection analyses showed that Z. palatalis tended to prefer valley and slope habitats over the plateau and that the proportion of point locations was significantly higher for adults in the slope habitat and for juveniles in the valley habitat. Most home ranges were centred on the ecotone between these two habitat types. Although isolated and spatially limited, these habitat patches provide high-quality resources for dense populations of Z. palatalis. This study exemplifies a species' attempt to make efficient use of a limited resource in an otherwise hostile environment. Even small declines in habitat area or quality due to their vulnerability to fire would impact upon many animals.


2010 ◽  
Vol 32 (1) ◽  
pp. 10 ◽  
Author(s):  
Yumiko Asari ◽  
Christopher N. Johnson ◽  
Mark Parsons ◽  
Johan Larson

The mahogany glider (Petaurus gracilis) is one of the most threatened arboreal mammals in Australia. Although its habitat is affected by fragmentation, gap-crossing behaviour of the species has not been studied. A radio-tracking survey was undertaken on six individuals (three males, three females) in a woodland patch bisected by a 35.8-m-wide highway and a 31.5-m-wide powerline corridor, in north-east Queensland. The mean home ranges of males were 20.1 ± 3.3 ha, 21.3 ± 7.9 ha and 20.9 ± 8.2 ha, as measured by the Minimum Convex Polygon, Kernel and Harmonic Mean methods respectively. The mean home ranges of females were 8.9 ± 0.5 ha, 9.0 ± 4.2 ha and 8.8 ± 2.3 ha, as measured by the Minimum Convex Polygon, Kernel and Harmonic Mean methods respectively. Two males and one female were observed crossing linear gaps. However, there was less crossing than expected, and females were less likely to cross than males. One male used a narrow strip of woodland at the opposite side of the highway as supplemental habitat for foraging. This individual also used scattered trees in a grassland matrix for foraging or denning. Another male used a wooden power pole as a launching site to cross the highway. This study emphasises the importance of protecting large trees along linear barriers in open habitat, and suggests that gliding poles may be used to facilitate gap-crossing by mahogany gliders.


2005 ◽  
Vol 22 (1) ◽  
pp. 85-91 ◽  
Author(s):  
Edsel Amorim Moraes Junior ◽  
Adriano Garcia Chiarello

From August 2001 to July 2002 the home range and movements of seven Micoureus demerarae (Thomas, 1905) (three males and four females) were investigated using radio tracking in the União Biological Reserve, state of Rio de Janeiro, south-eastern Brazil. A total of 436 locations was obtained and home range estimated with fixed Kernel (95% of data points), and minimum convex polygon (MCP) methods, with 100 and 95% of data points. Male home ranges estimated by MCP (100%) ranged from 5.4-24.2 ha and females from 0.3-10.7 ha. Corresponding figures calculated with Kernel (95%) were 4-10.9 ha for males and 1.3-5.9 ha for females. Animals travelled on average 423 m/night, with males travelling significantly further (582.8 m/night) than females (335.1 m/night) (t test, t = 3.609, p = 0.001). We concluded that radio tracking produced much larger home ranges than those estimated with traditional live-trapping techniques, suggesting that the latter might underestimate ranging when the area covered with traps is relatively small (ca. 1 ha or less). Radio tracking also indicated that M. demerarae, although predominantly arboreal and weighting only ca. 130 g., has movements similar in magnitude to larger-sized terrestrial didelphimorph marsupials, such as Didelphis Linnaeus, 1758, Philander Linnaeus, 1758 and Metachirus (Desmarest, 1817).


Oryx ◽  
2014 ◽  
Vol 48 (3) ◽  
pp. 370-377 ◽  
Author(s):  
Achara Simcharoen ◽  
Tommaso Savini ◽  
George A. Gale ◽  
Saksit Simcharoen ◽  
Somphot Duangchantrasiri ◽  
...  

AbstractTigers Panthera tigris are highly threatened and continue to decline across their entire range. Actions to restore and conserve populations need to be based on science but, in South-east Asia, information on ecology and behaviour of tigers is lacking. This study reports the relationship between the home range size of female tigers and prey abundance, using data from radio-collared tigers in Huai Kha Khaeng Wildlife Sanctuary, Thailand, and published data from other studies. A total of 11 tigers, four males and seven females, were fitted with global positioning system collars, to estimate home ranges using 95 and 100% minimum convex polygons (MCP). Prey abundance was estimated by faecal accumulation rates. The mean home range size of male tigers was 267 and 294 km2 based on 95 and 100% MCPs, respectively; the mean female home range size was 70 and 84 km2, respectively. Territories of male and female tigers had little overlap, which indicated both sexes were territorial. Mean densities of the prey species sambar Rusa unicolor, barking deer Muntiacus muntjac and large bovids were 7.5, 3.5 and 3.0 km−2, respectively. When female home range size and prey abundance were compared at six locations in Thailand, and at other sites in India, Nepal, Bangladesh and Russia, a significant negative correlation was found between prey abundance and home range size. Monitoring this relationship can provide managers with metrics for setting conservation goals.


2007 ◽  
Vol 17 (1) ◽  
pp. 63-77 ◽  
Author(s):  
MARTIN GILBERT ◽  
RICHARD T. WATSON ◽  
SHAKEEL AHMED ◽  
MUHAMMAD ASIM ◽  
JEFF A. JOHNSON

The provision of supplementary food at vulture restaurants is a well-established tool in the conservation of vulture species. Among their many applications, vulture restaurants are used to provide a safe food source in areas where carcasses are commonly baited with poisons. Rapid and extensive declines of vultures in the Indian subcontinent have been attributed to the toxic effects of diclofenac, a pharmaceutical used in the treatment of livestock, to which vultures are exposed while feeding on the carcasses of treated animals. A vulture restaurant was established at the Oriental White-backed Vulture Gyps bengalensis colony at Toawala, in Punjab province Pakistan, to test the effectiveness of the technique in modifying ranging behaviour and mortality at the colony. Six male vultures were fitted with satellite transmitters to describe variation in movement and home-range during periods when safe food was alternately available and withheld at the vulture restaurant. There was considerable variation in individual home-range size (minimum convex polygons, MCP, of 1,824 km2 to 68,930 km2), with birds occupying smaller home-ranges centred closer to the restaurant being more successful in locating the reliable source of food. Fixes showed that 3 of the tagged vultures fed at the vulture restaurant and the home-range of each bird declined following their initial visit, with a 23–59% reduction in MCP. Mean daily mortality during provisioning was 0.072 birds per day (8 birds in 111 days), compared with 0.387 birds per day (41 birds in 106 days) during non-provisioning control periods. Vultures tended to occupy greater home-ranges, cover greater distances each day and spend proportionately more time in the air during the late brooding and post-breeding seasons. Attendance at the vulture restaurant also declined during this period with fewer birds visiting less often and no tagged vultures visiting the vulture restaurant at all. These findings indicate that vulture restaurants can reduce, but not eliminate, vulture mortality through diclofenac exposure and represent a valuable interim measure in slowing vulture population decline locally until diclofenac can be withdrawn from veterinary use.


2018 ◽  
Vol 12 (1) ◽  
pp. 1-7
Author(s):  
Marek Kouba ◽  
Václav Tomášek

Abstract Animal home ranges are typically characterized by their size, shape and a given time interval and can be affected by many different biotic and abiotic factors. Understanding of animal movements and assessing the size of their home ranges are essential topics in ecology and necessary for effective species protection, especially concerning birds of prey. Using radio-telemetry (VHF; 2.1 g tail-mounted tags) we studied the movements of two Tengmalm’s owl (Aegolius funereus) males during the breeding season 2008 in a mountain area of Central Europe (the Czech Republic, the Jizera Mountains: 50˚ 50’ N, 15˚ 16’ E). We determined their average nocturnal hunting and diurnal roosting home range sizes. The mean hunting home range size calculated according to the 90% fixed kernel density estimator was 251.1 ± 43.2 ha (± SD). The mean roosting home range size calculated according to the 100% minimum convex polygon method was 57.9 ± 15.8 ha (± SD). The sizes of hunting home ranges during breeding in this study coincide with those previously reported by other studies focusing on Tengmalm’s owl males. However, we found the roosting home ranges were smaller in size compared to those previously reported. This result was most probably connected with different habitat structure in our study area, which was severally damaged by air-pollution in the past, thus probably offering fewer suitable hiding-places, for instance from predators. We found the roosting locations were concentrated in the oldest and densest Norway spruce forest patches. We emphasize that these parts of forest stands require the highest possible protection in our study area.


2003 ◽  
Vol 25 (2) ◽  
pp. 183 ◽  
Author(s):  
Mar K le ◽  
C McArthur ◽  
M Statham

We investigated home ranges of sympatric red-necked (or Bennett?s) wallabies Macropus rufogriseus rufogriseus, red-bellied pademelons Thylogale billardierii and common brushtail possums Trichosurus vulpecula fuliginosus within a forestry environment in north-west Tasmania. Six indiviuals of each species were radio-tracked between 7 and 11 months. Nocturnal and diurnal data were used to estimate Minimum Convex Polygon (MCP) home range, 95% fixed-Kernel (KE) home range and 50% KE core area. Home ranges (mean � s.e.) were as follows: M. r. rufogriseus MCP = 61 � 12 ha, KE = 41 � 3 ha; T. billardierii MCP = 22 � 5 ha, KE = 16 � 3 ha; and Tr. v. fuliginosus MCP = 39 � 8 ha, KE = 17 � 3 ha. M. r. rufogriseus had larger MCP home ranges than T. billardierii (P < 0.05), and larger KE home ranges and core areas than both T. billardierii and Tr. v. fuliginosus (P < 0.05), which reflected their larger body mass. Inter-sexual comparisons within the sexually dimorphic macropods showed that M. r. rufogriseus males had significantly larger MCP and KE home ranges and core areas than females (P < 0.05), and T. billardierii males tended to have a larger KE home ranges than females (P = 0.08). No inter-sexual difference in home range size was detected for Tr. v. fuliginosus.


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.


2007 ◽  
Vol 34 (6) ◽  
pp. 472 ◽  
Author(s):  
Geoffrey C. Smith ◽  
Michael Mathieson ◽  
Luke Hogan

Greater gliders, Petauroides volans, were radio-tracked within a large tract of forest in the dry inland of southern Queensland. This forest has been commercially logged for timber for more than 100 years. Home-range estimates ranged from 1.4 ha (female) to 19.3 ha (male). Minimum convex polygon (MCP) estimates were larger for males (average, 11.5 ha) than females (average, 3.3 ha) and combined (6.8 ha, sexes pooled) were larger than estimates from other Australian populations. Gliders were located foraging in myrtaceous tree species only, using mostly Eucalyptus moluccana, E. fibrosa and Corymbia citriodora. E. moluccana was used for foraging more frequently than would be expected on the basis of its availability in the forest. E. fibrosa and C. citriodora were used in proportion to their availability in the forest. Gliders were not seen foraging in non-myrtaceous species or myrtaceous trees <20 cm diameter at breast height (dbh), preferring trees in 30–70-cm dbh classes and as ‘mature’ and ‘over-mature’ classified according to growth-stage characteristics. Den tree species included the same species used for foraging as well as dead trees (16% of den trees). E. fibrosa and E. tereticornis were preferred significantly more than expected by their availability in the forest. Non-myrtaceous species were not used as live den trees. Large (dbh >50 cm) and old living trees (in deteriorating and senescent condition: ‘late mature’ and ‘over-mature’ categories) were primarily used as den trees. Individual gliders utilised 4–20 den trees. Females utilised more den trees per unit area of home range (3.8 den trees ha–1, maximum) than males (0.9 den trees ha–1, maximum). Fewer den trees were used per unit area of home range than by gliders at a coastal location with approximately the same latitude. The density of live stems containing hollows suitable as dens is currently lower than 1 tree ha–1 in some parts of the study forest. Gliders were two and half times less likely to be observed during standardised spotlighting surveys in the study area than elsewhere in southern Queensland. It is likely that low availability of den trees is contributing to large home ranges and the apparent low population density observed in this study.


2002 ◽  
Vol 8 (4) ◽  
pp. 271 ◽  
Author(s):  
Peter G. Cale

White-browed Babbler Pomatostomus superciliosus groups occupying linear strips of vegetation had breeding territories that were smaller in area and had longer linear dimensions than those occupying patches. A group's non-breeding home range was larger than its breeding territory. Groups occupying linear/patch home ranges expanded the linear extent and area of their home ranges more than those within other home range configurations. Some groups moved during the non-breeding season and this was more likely to occur if the group occupied a remnant with a low abundance of invertebrates during summer. Some groups that moved returned prior to the next breeding season, but the majority were never seen again. New groups moved into the study sites and established in vacant home ranges. This suggests that those groups that left the study sites may have established new home ranges elsewhere. Breeding site fidelity was lower in groups that had failed in previous breeding attempts. Therefore, group movements were influenced by the feeding and breeding quality of the habitat. However, the configuration of the local population also influenced group movements with those groups on the edge of a local population being more likely to move than those in the interior. New groups were formed by two processes; group dispersal, where groups generally filled a vacant home range, and group budding, which involved the splitting of a large group. Group dispersal maintained group densities while group budding increased the density of groups in a local population. These two processes were common, producing localized fluctuations in the density of groups. Since babbler groups contain only one breeding pair, changes in group density represent changes in effective population size. Therefore, group dynamics may be important to the persistence of local populations of White-browed Babblers, especially in landscapes that have suffered from habitat loss and fragmentation.


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