scholarly journals Female tiger Panthera tigris home range size and prey abundance: important metrics for management

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.

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.


2008 ◽  
Vol 122 (1) ◽  
pp. 61 ◽  
Author(s):  
Matthew Schuler ◽  
Richard P. Thiel

Most studies of home ranges occur over short time periods and may not represent the spacial requirements of long-lived organisms such as turtles. Home ranges of 18 individual Blanding’s Turtles (Emydoidea blandingii) were measured using minimum convex polygons. Annual space use was compared to multi-year space use by individual turtles. We found a significant difference between annual home range size (25.5 hectares) and multi-year (two to six years) home range size (65.7 hectares; n = 18, P = 0.016). Caution should be employed when making management decisions based on short-term studies of long lived species.


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.


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.


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.


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.


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.


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.


Author(s):  
Jordan Clark Rabon ◽  
Cassandra M. V. Nuñez ◽  
Peter Coates ◽  
Mark Ricca ◽  
Tracey N. Johnson

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.


1995 ◽  
Vol 52 (7) ◽  
pp. 1499-1508 ◽  
Author(s):  
Charles K. Minns

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.


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