Home range, burrow-use and activity patterns in common wombats (Vombatus ursinus)

2008 ◽  
Vol 35 (5) ◽  
pp. 455 ◽  
Author(s):  
Murray C. Evans
Keyword(s):  
Home Range ◽  
Activity Patterns ◽  
Movement Pattern ◽  
Home Range Size ◽  
Low Energy ◽  
Harmonic Mean ◽  
Home Ranges ◽  
Eucalypt Forest ◽  
Ranging Behaviour ◽  
Burrow Use

Wombats are large, marsupial herbivores able to exploit low-productivity habitats largely because of their low energy requirements. In addition to using deep, thermally favourable burrows, wombats might use a strategy of conservative above-ground ranging behaviour to achieve their low energy expenditure. This study examined home range, burrow use and diurnal activity patterns of common wombats (Vombatus ursinus) in eucalypt forest, woodland and pasture using trapping and radio-tracking. Wombats ranged through all three vegetation types with forest and pasture clearly being important habitats. Home ranges (95% harmonic mean) were typically almost circular, and averaged 17.7 ha with core areas (50% harmonic mean) averaging 2.9 ha. Home-range size is small compared with that expected for most mammals of comparable body mass. Ranging behaviour for wombats was similar between sexes and ranges extensively overlapped between and within sexes, indicating that ranges are not actively defended. Wombats did not markedly change the size or location of home ranges, ranging behaviour or feeding areas between summer and winter. The density of active burrows (0.25 ha–1) far exceeded the estimated density of wombats (0.13 ha–1). Wombats typically spent 1–4 days sleeping in the same burrow and then moved to another. On average, each active burrow was used by 2.2 different individuals. The activity pattern of wombats is characterised by a strong diel cycle, with most activity occurring nocturnally. Activity peaks at the beginning and end of each night are consistent with a ‘travel out, graze, travel back’ movement pattern. Despite widely distributed food resources, small home ranges and obligate burrow use constrain wombats to meeting their year-round food and water requirements from a small area near their burrows.

Movement patterns of feral predators in an arid environment – implications for control through poison baiting

2009 ◽  
Vol 36 (5) ◽  
pp. 422 ◽  
Author(s):  
K. E. Moseby ◽  
J. Stott ◽  
H. Crisp
Keyword(s):  
Home Range ◽  
Sand Dunes ◽  
Activity Patterns ◽  
Movement Patterns ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Feral Cats ◽  
Poison Baiting ◽  
Specific Variation

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.

Snowmobile Effects on Movements of White-tailed Deer: A Case-study

1979 ◽  
Vol 6 (1) ◽  
pp. 45-51 ◽  
Author(s):  
Ronald G. Eckstein ◽  
Thomas F. O'Brien ◽  
Orrin J. Rongstad ◽  
John G. Bollinger
Keyword(s):  
Home Range ◽  
Habitat Use ◽  
Odocoileus Virginianus ◽  
Activity Patterns ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges

The effects of snowmobile traffic on the winter home-ranges, movements, and activity patterns, of White-tailed Deer (Odocoileus virginianus), were studied during two winters in northern Wisconsin. There were no significant differences in home-range size and habitat use of the Deer in areas with and without snowmobiling. However, snowmobiling caused some Deer to leave the immediate vicinity of the snowmobile trail. Deer were most affected when they were within 61 m of the snowmobile trail.

Movement patterns and spatial organisation of the mulgara, Dasycercus cristicauda (Marsupialia : Dasyuridae), in central Australia

2003 ◽  
Vol 30 (4) ◽  
pp. 339 ◽  
Author(s):  
Pip Masters
Keyword(s):  
Home Range ◽  
Radio Telemetry ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Average Maximum ◽  
High Site ◽  
Central Australia ◽  
Burrow Use ◽  
Solitary Species

Information on the movements, social structure and burrow use of the mulgara, Dasycercus cristicauda, was collected using radio-telemetry at two study areas in central Australia, one located near the Granites gold mine in the Tanami Desert and the other located on the edge of Uluru Kata Tjuta National Park. The average home-range size was not significantly different between the two study areas but home-range size was highly variable amongst individuals, with areas from 1.0 to 14.4 ha being used. The average maximum distance moved was significantly greater for males than for females. Overlap of home ranges was less than 20%, on average, but this was highly variable. There was an average overlap of 14% for females, with a maximum of 67%. The home ranges of males also overlapped, averaging 16.5%, as did those of females and males (19%). D. cristicauda is a solitary species that exhibits high site fidelity and a low propensity for dispersal once a home range has been established.

Home range of the swamp wallaby, Wallabia bicolor

1993 ◽  
Vol 20 (5) ◽  
pp. 571 ◽  
Author(s):  
S Troy ◽  
G Coulson
Keyword(s):  
Home Range ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Convex Polygons ◽  
Minimum Convex Polygon ◽  
Eucalypt Forest ◽  
Significant Difference ◽  
Wallabia Bicolor ◽  
Swamp Wallaby

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.

Translocation of a top-order carnivore: tracking the initial survival, spatial movement, home-range establishment and habitat use of Tasmanian devils on Maria Island

2016 ◽  
Vol 38 (1) ◽  
pp. 68 ◽  
Author(s):  
Sam Thalmann ◽  
Sarah Peck ◽  
Phil Wise ◽  
Joanne M. Potts ◽  
Judy Clarke ◽  
...  
Keyword(s):  
Home Range ◽  
Key Management ◽  
Movement Pattern ◽  
Positive Association ◽  
Home Range Size ◽  
Habitat Associations ◽  
Ex Situ ◽  
Tasmanian Devil ◽  
Eucalypt Forest ◽  
Devil Facial Tumour Disease

The Tasmanian devil (Sarcophilus harrisii) is a carnivorous marsupial threatened with extinction from the emergence of Devil Facial Tumour Disease. The establishment of ex situ populations is a key management action for the species. We examined the initial survival, movement pattern, home range, and habit use of six devils from a total of 15 individuals translocated to Maria Island (south-east Tasmania). A total of 14 devils (93%) survived the initial monitoring phase within this study (122 days after translocation). The maximum and minimum distance recorded during one night was 21.73 km (range = 14.12–25.40 km) and 1.94 km (range = 0.07–7.71 km), respectively, while the average nightly distance travelled varied significantly (range = 7.24–13.07 km) between individuals. Short-term home-range size (90% kernel) varied from 936 to 3501 ha, with an average of 2180 (±836) ha for all devils. The habitat preference of devils on Maria Island shows a positive association with agricultural and urban habitats, and an avoidance of wet eucalypt forest. The home range and habitat associations may change as competitive pressures increase with population growth; however, this initial research indicates that translocation as a management action is a powerful tool for the establishment of ex situ populations, assisting in the continued conservation of this species.

Ecological Correlates of Fecal Corticosterone Metabolites in Female Greater Sage-Grouse (Centrococercus urophasianus)

2021 ◽  
Author(s):  
Jordan Clark Rabon ◽  
Cassandra M. V. Nuñez ◽  
Peter Coates ◽  
Mark Ricca ◽  
Tracey N. Johnson
Keyword(s):  
Home Range ◽  
Stress Responses ◽  
Habitat Degradation ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Remotely Sensed Data ◽  
Sage Grouse ◽  
Ecological Conditions ◽  
Annual Grasses

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.

scholarly journals Home Ranges and Movements of Elk (Cervus canadensis) Restored to Southern Ontario, Canada

2017 ◽  
Vol 130 (4) ◽  
pp. 320 ◽  
Author(s):  
Rick Rosatte
Keyword(s):  
Home Range ◽  
Home Range Size ◽  
Home Ranges ◽  
Winter Range ◽  
The Social ◽  
Cervus Canadensis ◽  
Summer Range ◽  
Seasonal Basis ◽  
Social Units ◽  
Winter Feeding

During 2000 and 2001, Elk (Cervus canadensis) were restored to the Bancroft, Ontario area. The objective of this study was to determine the home range and movements of six social units of Elk, 5–12 years after restoration, in an area of about 2500 km2 near Bancroft. Home range and movements were calculated from 40 221 Global Positioning System locations acquired from 56 collared Elk (16 bulls and 40 cows) between 2006 and 2013. Annual home ranges were found to be significantly greater (mean 110.3 km2, standard error [SE] 11.2) for Elk in areas where winter feeding by humans did not occur compared with those (mean 51.0 km2, SE 9.0) where winter feeding was prevalent. Elk in winter feeding areas had smaller ranges in winter than other seasons. On a seasonal basis, home range size was larger for Elk in areas where winter feeding did not occur; mean winter home range for Elk in non-feeding areas was 73.4 km2 (SE34.0) compared with 8.3 km2 (SE 2.6) for Elk in areas where winter feeding occurred. The 20 Elk that were monitored for multiple years exhibited home range fidelity among years. The entire range of all radio-collared Elk within the social groups studied covered 1716.4 km2 during 2006–2013. Average daily movements of Elk in the study arearanged from 1.0 to 2.1 km/day with greatest movements occurring during spring and summer. However, some Elk were capable of moving an average of 5–7km in a 12-h interval. Movements (about 5 km) to winter range occurred during October to December each year. Cows moved to calving areas in May with mean movements of Elk to spring/summer range about 6 km. Cow/calf groups moved to fall ranges by early September with mean movements of about 4 km. During the rut, mean bull movements of 16.0 km to cow groups over 1–5 days occurred in early September. Hunting of Elk during the fall of 2011 and 2012 did not appear to significantly affect the movements and dispersion of Elk in the study area.

Allometry of home range size in lake and river fishes

1995 ◽  
Vol 52 (7) ◽  
pp. 1499-1508 ◽  
Author(s):  
Charles K. Minns
Keyword(s):  
Body Size ◽  
Home Range ◽  
Freshwater Fish ◽  
Fish Population ◽  
Home Range Size ◽  
Range Size ◽  
Territory Size ◽  
Home Ranges ◽  
Data Set ◽  
Terrestrial Mammals

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.

Influence of habitat on home-range size in the short-beaked echidna

2012 ◽  
Vol 60 (1) ◽  
pp. 46 ◽  
Author(s):  
Jenny Sprent ◽  
Stewart C. Nicol
Keyword(s):  
Home Range ◽  
Spatial Ecology ◽  
Habitat Type ◽  
Negative Relationship ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Location Data ◽  
Significant Negative Relationship ◽  
Solitary Species

The size of an animal’s home range is strongly influenced by the resources available within it. In productive, resource-rich habitats sufficient resources are obtainable within a smaller area, and for many species, home ranges are smaller in resource-rich habitats than in habitats with lower resource abundance. Location data on 14 male and 27 female echidnas (Tachyglossus aculeatus) fitted with tracking transmitters, in the southern midlands of Tasmania, were used to test the influence of habitat type on home-range size. We hypothesised that as woodland should offer more shelter, food resources and refuges than pasture, echidnas living in woodland would have smaller home ranges than those living in pasture areas. We found significant differences between the sexes. Male echidnas had a significantly larger mean home range than females and a quite different relationship between home-range size and habitat type from females. There was no relationship between the proportion of woodland within male home ranges and home-range size whereas female echidnas had a highly significant negative relationship. This suggests that home-range size of female echidnas is highly influenced by the amount of woodland within it, but the home-range size of male echidnas is controlled by factors other than habitat. This pattern is consistent with the spatial ecology of many other solitary species with a promiscuous mating system. The home ranges of females are scaled to encompass all necessary resources for successfully raising their young within a minimal area, whilst the large home ranges of males are scaled to maximise access to females.

scholarly journals Home range expansion in response to temperature by evening bats (Nycticeius humeralis) in an urban environment

2020 ◽  
Author(s):  
Ellen Hall ◽  
Victoria Bennett
Keyword(s):  
Water Resources ◽  
Home Range ◽  
Urban Areas ◽  
Home Range Size ◽  
Range Size ◽  
Green Spaces ◽  
Activity Period ◽  
Home Ranges ◽  
Urban Green ◽  
Urban Green Spaces

Abstract Background: Despite the negative connotation of urban sprawl for bat populations, fragmented green spaces such as parks, cemeteries, and golf courses have the potential to provide necessary resources for bats. For example, water resources in these areas can include natural or semi-natural lakes, ponds, streams, and drainage ditches. Such water resources, however, are frequently ephemeral when subject to prolonged periods of high temperatures. We, therefore, hypothesize that bats will expand or shift their home ranges from these urban green spaces into the surrounding neighborhoods to access alternative resources, such as residential swimming pools. Methods: To explore whether bats expand their ranges from urban green spaces, we conducted a telemetry study in which we radio-tracked resident evening bats (Nycticeius humeralis) in a local park system during their summer activity period from 2017-2019 in Fort Worth, Texas, USA. From radio-tracking surveys, we measured home range size using a k-LoCoH method and the percentage of these home ranges that fell within the park system. We compared these variables using linear and non-linear regressions with temperature. Results: We successfully tracked a total of 30 bats over the 3-year period and found a positive correlation between home range size and temperature. Furthermore, we observed that home ranges increased 6 times in size when temperatures exceeded 30ºC. Conclusions: Our study indicates the importance of urban neighborhoods surrounding green spaces in providing alternative resources, such as water, for bats. If managed appropriately, these urban areas have the potential to act as urban oases for bat populations, which in turn can contribute to their conservation.

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