Denning and home-range characteristics of breeding arctic foxes in Svalbard

1992 ◽  
Vol 70 (7) ◽  
pp. 1276-1283 ◽  
Author(s):  
Pål Prestrud

Home range, den density, and use of dens of arctic foxes (Alopex lagopus) in Svalbard were investigated through systematic den surveys, ear tagging of pups, and tracking of radio-collared animals. The mean home range for three breeding vixens was 48 km2. Home-range estimates based on occupied dens were between 46 and 75 km2. This is larger than recorded for arctic foxes elsewhere, and may be related to the absence of small mammals and, consequently, to a more scattered prey base in Svalbard. Home-range size was apparently not related to variations in the availability of food among years or among seasons. The density of all dens recorded was 1/24 km2. As a consequence of landscape patterns, these dens were more clustered than if they were randomly dispersed. However, dens with litters in 1986 (1 den/75 km2) were more widely spaced than if randomly distributed, indicating territoriality among arctic foxes. Most dens were in use throughout the year. Some litters were relocated or subdivided among several dens.

2006 ◽  
Vol 75 (6) ◽  
pp. 1393-1405 ◽  
Author(s):  
LUCA BÖRGER ◽  
NOVELLA FRANCONI ◽  
GIAMPIERO DE MICHELE ◽  
ALBERTO GANTZ ◽  
FIORA MESCHI ◽  
...  

Koedoe ◽  
1982 ◽  
Vol 25 (1) ◽  
Author(s):  
B. L Penzhorn

The mean home range size of Cape mountain zebra breeding herds was 9,4 km2 (range 3,1 @ 16,0 km2). In two herds which split up, the home ranges of the resultant herds included the original home ranges, but were larger.


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.


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.


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.


2006 ◽  
Vol 27 (2) ◽  
pp. 255-261 ◽  
Author(s):  
◽  
◽  
◽  
◽  

AbstractHome range and nesting habitat were studied in two sympatric pelomedusid terrapins (Pelusios niger and Pelusios castaneus) from two study areas in the Niger Delta (Nigeria, West Africa), one with pristine habitat conditions and one which was polluted by a oil spill event some years before. Seventy-seven individuals (38 P. niger and 39 P. castaneus) were radiotracked, each for more than 60 days, and their home range was calculated by the minimum convex polygon method, with 95% of the point locations per individual. The mean home range size of females was significantly larger in the polluted area than in the pristine area in both P. niger and P. castaneus, and the mean home range size of female P. niger was significantly larger than that of female P. castaneus in the polluted area, but not in the pristine area. The mean home range size of males was significantly larger in the polluted area than in the pristine area in P. niger but not in P. castaneus, and the mean home range size of male P. niger was significantly larger than that of male P. castaneus in the polluted area but not in the pristine area. Radiotracked females of both species showed a clear preference for nesting sites situated along ponds and not along the banks of the river, on sandy soil, often with abundant vegetation around. Some females of both species deposited their eggs at greater distances from water bodies in the polluted area than in the pristine area. The comparative evidence of these patterns indicates consistent responses of the two species to the altered habitat, which further supports the general hypothesis that habitat pollution has seriously affected the ecological strategies of these terrapin species.


2021 ◽  
Vol 75 (8) ◽  
Author(s):  
Tomasz Borowik ◽  
Rafał Kowalczyk ◽  
Weronika Maślanko ◽  
Norbert Duda ◽  
Mirosław Ratkiewicz

Abstract The heterogeneity of resource availability shapes animal movements at different spatio-temporal scales. Given that movements at various scales are assumed to be linked, the space use of temperate ungulates within seasonal ranges (winter, summer) should be related to their movement patterns at the annual scale. In this study, we aimed to evaluate the level of stationarity of moose (Alces alces) within their seasonal ranges and to link annual movement patterns to within-season space use. We analysed the ranging behaviour of 32 moose fitted with GPS collars from two study areas in Eastern Poland, where at the annual scale a fraction of individuals migrate between summer and winter ranges (partial migration). Our results revealed that moose stationarity within seasonal home ranges expressed remarkable variation. The probability of moose stationarity within seasonal ranges was significantly higher (by 23%), and the mean home range size tended to be lower (9.7 km2) among individuals that seasonally migrated than among non-migratory moose (14.3 km2). In addition, we found that (i) in summer, moose were significantly more stationary (by 19%) and exhibited a smaller mean home range size than in winter (9.0 and 15.9 km2, respectively) and (ii) the mean seasonal home range size of males (19.6 km2) was remarkably greater than that of females (9.6 km2). Given the significant link between annual and seasonal scales of animal movements, any environmental change (e.g. climate warming) affecting an animal’s annual movement strategy could alter within-season animal space use and presumably individual fitness. Significance statement To maximize their fitness, animals adjust their movements to deal with variations in resource distribution in the landscape. The scale of spatio-temporal variation causes different types of migratory behaviours, ranging from year-round stationarity to migration, when individuals establish spatially separated seasonal ranges. Studies on ungulates suggest that the stability and the size of seasonal home ranges can be linked to annual movement behaviour. Using the locations of GPS-tracked moose, we demonstrate in this study that migratory individuals were more prone to establishing stable seasonal home ranges (especially in summer) than moose that occupied the same area throughout the year. Moreover, stable seasonal home ranges were remarkably smaller in summer than in winter, which may suggest a season-specific spatial distribution and a renewability of moose forage. Our results show a clear link between different temporal scales of animal movements.


2016 ◽  
Vol 56 (6) ◽  
pp. 988 ◽  
Author(s):  
Xin He ◽  
Min Chen ◽  
Endi Zhang

The Chinese water deer was once widely spread in Liaodong Peninsula, North China Plain and both banks of the Yangtze River and the Korean peninsula. Due to long-term environmental changes and influence of human development, its wild population in China has rapidly declined, both in abundance and distribution. As one of the native species in the history of Shanghai, Chinese water deer was introduced to Shanghai for captive breeding in 2006 and were released into the wild in 2010. The present study was conducted in Nanhui East Shoal Wildlife Sanctuary. The reintroduction of Chinese water deer was carried out separately in June and October 2010. So as to study the movement of the deer after release, 12 Chinese water deer (sex ratio 1 : 1) were tagged with radio-collars. We successfully used radio-telemetry to track 10 deer, and used the minimum convex polygon (MCP) and fixed kernel estimation (FKE) methods to calculate their home range. The results showed that using the MCP method, the mean home-range size of Chinese water deer was estimated to be 671 ha (range 245–1559 ha), while using the 95% FKE method, the mean was estimated to be 262 ha (range 43–435 ha). The mean home-range size of a buck was smaller than that of a doe by both MCP and FKE. The mean home-range size of an adult female was smaller than that of a subadult female. The largest seasonal home-range size (MCP, 275 ha) occurred during the winter of the first year, which then kept on shrinking in spring and summer. Home-range overlap was found among the home range of each individual. The mean overlap size was 303 ha. The mean overlap size was 135 ha in bucks, 422 ha in does and 270 ha between the buck and the doe. The study reflects that the seasonal food change is probably the main factor for the change of home-range size. Oestrus may also result in the enlargement of home range in winter. As an attempt to reintroduce large mammals to cities, we hope to provide useful experience for future wildlife management and conservation.


2006 ◽  
Vol 54 (4) ◽  
pp. 225 ◽  
Author(s):  
Jennifer K. Martin

Detailed knowledge of how individuals use space when active and while sheltering is crucial to understanding the habitat requirements of a species. I present the first home-range estimates for bobucks, Trichosurus cunninghami, that are based on both nocturnal and diurnal radio-tracking fixes. I tracked 37 individuals (14 adult females, 14 adult males, three subadult females and six subadult males) between mid-1999 and late 2003 in a forest patch in the Strathbogie Ranges, south-eastern Australia. I collected a total of 9562 diurnal fixes (mean 309 fixes per adult) and 5211 nocturnal fixes (mean 169 fixes per adult). All individuals used multiple den-trees; adults used a mean of 7.2 den-trees per individual. Adult bobucks of both sexes had a mean home-range size of 6.0 ha. There were no significant differences in the mean number of den-trees used or in the mean home-range size of adult males and females. Subadults used significantly fewer den-trees and had significantly smaller home ranges than adults. This study demonstrates the importance of large and long-term datasets in accurately determining the habitat requirements of a population.


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