Home range and microhabitat use by the long-footed potoroo, Potorous longipes

1998 ◽  
Vol 25 (4) ◽  
pp. 357 ◽  
Author(s):  
K. Green ◽  
A. T. Mitchell ◽  
P. Tennant
Keyword(s):  
Home Range ◽  
Environmental Changes ◽  
Home Range Size ◽  
Microhabitat Use ◽  
Radio Tracking ◽  
Geographical Differences ◽  
Eucalypt Forest ◽  
Old Growth Forest ◽  
Minimum Numbers ◽  
Trapping Grid

Long-footed potoroos were studied at two widely-separated sites in Victoria, one in regenerating eucalypt forest in East Gippsland and the other in old-growth forest in Central Gippsland. Trap-revealed use of microhabitat at Bellbird (East Gippsland) showed a change from the 1980s to 1990s, with an increased amount of foraging in more open, drier areas. Over the same period, there was an increase in the size of home range of animals and a near-doubling of the minimum numbers of animals known to be alive on the trapping grid at Bellbird. These changes occurred over a period when few environmental changes occurred on the grid other than control of feral predators. Radio-tracking data from 12 animals at the two sites showed a similar trend in use of microhabitat by most animals, but there was individual variation. Differences between the sites were that home-range size was smaller at the Riley trapping grid (Central Gippsland), there was greater overlap in home range, and animals there foraged for significantly shorter bouts. This confirmed earlier speculation from reproductive and dietary studies that there is better quality habitat at Riley, but the sites were so dissimilar that differences in home range and foraging could not be ascribed to either the logging regime or to geographical differences between the sites.

Home ranges and movement schedules of sympatric bridled nailtail and black-striped wallabies

1996 ◽  
Vol 23 (5) ◽  
pp. 547 ◽  
Author(s):  
M Evans
Keyword(s):  
Home Range ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Radio Tracking ◽  
Wet Season ◽  
Seasonal Differences ◽  
Dry Seasons ◽  
Species Movement ◽  
Wet And Dry Seasons

Home ranges and movement schedules of sympatric bridled nailtail wallabies, Onychogalea fraenata, and black-striped wallabies, Macropus dorsalis, were studied during wet and dry seasons by radio-tracking. Home ranges of black-striped wallabies (91 ha) were much larger than those of bridled nailtail wallabies (40 ha). Home-range size differed between sexes for bridled nailtail wallabies (males, 59 ha; females, 26 ha), but not for black-striped wallabies. Intraspecific seasonal differences in home-range size were not significant. All home ranges included diurnal shelter habitat, although the preferred type of shelter habitat was different for each species. Movement schedules differed significantly between wet and dry seasons for black-striped wallabies (which made a higher frequency of longer-distance movements during the dry season than during the wet season), but not for bridled nailtail wallabies.

Knowledge of habitat preferences applied to habitat management: the case of an endangered tortoise population

2015 ◽  
Vol 36 (1) ◽  
pp. 13-25 ◽  
Author(s):  
Albert Vilardell-Bartino ◽  
Albert Vilardell-Bartino ◽  
Xavier Capalleras ◽  
Albert Vilardell-Bartino ◽  
Xavier Capalleras ◽  
...  
Keyword(s):  
Home Range ◽  
Iberian Peninsula ◽  
Habitat Management ◽  
Habitat Preferences ◽  
Home Range Size ◽  
Range Size ◽  
Activity Period ◽  
Microhabitat Use ◽  
Management Decisions ◽  
Barren Land

To avoid the possible extinction of the last native population of western Hermann’s tortoise in the Iberian Peninsula it is essential to make sound management decisions. Knowledge of macro and microhabitat use and home range size has considerable practical value for land managers. With this aim we first studied the home range and habitat preferences in western Hermann’s tortoises by radio tracking 15 adults weekly from March 2008 to May 2009 in three localities within the Albera population range (NE Iberian Peninsula). We estimated home ranges with Fixed Kernel estimator (FK) and Minimum Convex Polygon (MCP) after checking tortoise site fidelity. We observed that home range size did not differ significantly between males and females (mean FK = 2.01 ha, mean MCP = 3.01 ha). Secondly, we studied macrohabitat selection using a vegetation map. Preferred habitats were open shrubland, open forest and barren land during the activity period, and dense forest, dense shrubland and open shrubland during the hibernation. Next, we assessed microhabitat selection along five periods of the annual cycle: hibernation, emergence from hibernation, spring, summer and autumn. We then located marked tortoises weekly and classified the plant species observed in each location. Principal component analyses showed that tortoises selected shrubs with trees during hibernation, bramble during summer and herbaceous habitat during the breeding season. All these results can provide guidelines for management programs that set aside areas of habitat critical to conserve viable populations, although it is also important to prevent mortality from forestry works. We therefore tested a new brush cutter head accessory to achieve tortoise-safe undergrowth clearing. To this aim we distributed 52 frozen hybrid tortoises among eight plots of 100 m2, cleared six of these plots with the accessory and two without it, and evaluated the scars of the blade on caparaces. We observed no damage in plots that were cleared with the accessory but scars in most carapaces in the plots cleared without it (with potential mortality ranging from 40% in neonates to 100% in adults). These results outline the importance of supporting habitat management decisions with proper field studies.

Home range, nest use and activity of the Tasmanian bettong, Bettongia gaimardi

1993 ◽  
Vol 20 (1) ◽  
pp. 87 ◽  
Author(s):  
RJ Taylor
Keyword(s):  
Home Range ◽  
Plant Material ◽  
Home Range Size ◽  
Range Size ◽  
Ground Vegetation ◽  
Home Ranges ◽  
Regular Pattern ◽  
Radio Tracking ◽  
Tracking Period

Home range, nest use and activity of the Tasmanian bettong, Bettongia gaimardi, was investigated in northern Tasmania. During 3-week periods in August and November 1986 and February and May 1987 radio-tracking of six females and three males was undertaken, five of these being tracked in more than one period. Home ranges of males were larger than those of females. There was no indication of any major differences in home-range size or shifts in location of home ranges between seasons. Nightly patterns of movement were essentially random with distances of 500-600 m between half-hourly locations being not uncommon. Males occasionally showed a more regular pattern of movement possibly related to searching for oestrous females. Bettongs became active soon after dark. The number of hours spent active was greatest during May (79% of length of night) and lowest during November (93% of night). Bettongs occasionally rested at night between two bouts of activity. Nests are formed from a hollowed-out bundle of plant material and located under fallen trees, shrubs or logs, or under low shrubs or clumps of ground vegetation such as Lomandra. Individuals used 3-6 nests per 3-week tracking period. Nests were usually only used consecutively for one or two nights, and different nests were used to different extents. A different set of nests tended to be used in different months. Nests showed some tendency to be located at one end of the home range. Nesting areas used by different individuals overlapped.

Home-range studies in a reintroduced brush-tailed rock-wallaby (Petrogale penicillata) population in the Grampians National Park, Victoria

2011 ◽  
Vol 33 (2) ◽  
pp. 128 ◽  
Author(s):  
Jenny Molyneux ◽  
David A. Taggart ◽  
Anthony Corrigan ◽  
Sean Frey
Keyword(s):  
Home Range ◽  
National Park ◽  
Site Fidelity ◽  
Home Range Size ◽  
Range Size ◽  
Local Extinction ◽  
Home Ranges ◽  
Radio Tracking ◽  
Western Victoria ◽  
Species Ecology

In 2008, after 9 years of presumed local extinction, brush-tailed rock-wallabies (Petrogale penicillata) were reintroduced at Moora Moora Creek in the Grampians National Park, western Victoria. Since little is known about this species in Victoria, the reintroduction presented an important opportunity to gain information on the species’ ecology. Radio-tracking was undertaken and home range determined for three individuals released 11 months before this study and a further five individuals that were released at the commencement of the study in October 2009. Home-range size showed little variation amongst individuals, with a mean overall home range of 26 ha (±1.69, s.e.) and a mean core home range of 2.5 ha (±0.24, s.e.). Newly reintroduced individuals showed higher levels of association with wallabies from the same release and greater site fidelity when known conspecifics were close. Within 5 months of release, newly reintroduced animals showed home ranges similar in both size and distribution to those of animals released 11 months prior.

Home ranges and movements of red foxes in central Europe: stability despite environmental changes

1995 ◽  
Vol 73 (10) ◽  
pp. 1960-1966 ◽  
Author(s):  
Jean-Steve Meia ◽  
Jean-Marc Weber
Keyword(s):  
Home Range ◽  
Snow Cover ◽  
Central Europe ◽  
Rural Areas ◽  
Environmental Changes ◽  
Home Range Size ◽  
Territory Size ◽  
Home Ranges ◽  
Red Foxes ◽  
The Individual

Thirteen red foxes (Vulpes vulpes) were radio-tracked between September 1989 and August 1993 in the Swiss Jura mountains. Home ranges of subadult and adult resident foxes did not differ and were small (seasonal estimates 0.48–3.06 km2). A nomadic adult was also monitored; it used a significantly larger area (12.71–25.90 km2). In most cases, home range sizes did not vary seasonally and were not affected by drastic changes in food availability. That foxes maintain a constant territory size is in accordance with both the "contractor" and "obstinate" strategies. The small observed sizes suggest that after the eradication of rabies, rural areas of central Europe are very good habitats for foxes. In the absence of clumped feeding patches or constraining factors (e.g., deep snow cover), the foxes moved regularly throughout their home range, typically in a "non-oriented zigzag." The distance travelled per day seemed to be affected only by home range size (positive correlation) and occasionally, according to the individual, by weather or snow cover. On average, the foxes moved 3.9–12.0 km a day. Despite its significantly larger home range, the nomadic fox did not move more than the resident foxes; the physical characteristics of red foxes probably set a limit to the distance travelled daily.

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.

The Effect of an Intensive Shooting Exercise From a Helicopter on the Behaviour of Surviving Feral Pigs.

1996 ◽  
Vol 23 (4) ◽  
pp. 435 ◽  
Author(s):  
N Dexter
Keyword(s):  
Home Range ◽  
Sus Scrofa ◽  
New South ◽  
Home Range Size ◽  
Home Ranges ◽  
Diel Variation ◽  
Radio Tracking ◽  
Feral Pigs ◽  
South Wales ◽  
North Western

The hypothesis that disturbance from a shooting exercise using a helicopter will influence the behaviour of surviving feral pigs, Sus scrofa, was tested on a population of radio-collared feral pigs in north-western New South Wales. No significant differences existed in hourly distance moved by pigs, diel variation in distance moved by pigs, or home-range size of pigs, between a radio-tracking session conducted immediately before a shooting exercise from a helicopter and a radio-tracking session conducted during and after the exercise. The position of the home ranges of feral pigs did not appear to be affected by the shooting exercise, although several radio-collared feral pigs moved into and out of the study area between tracking sessions. Overall, the results suggest that the disturbance caused by shooting has little effect on the behaviour of surviving feral pigs.

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.

Home range and habitat use by Magellanic Woodpeckers in an old-growth forest of Patagonia

2014 ◽  
Vol 44 (10) ◽  
pp. 1265-1273 ◽  
Author(s):  
Valeria Ojeda ◽  
Laura Chazarreta
Keyword(s):  
Home Range ◽  
Woody Debris ◽  
Home Range Size ◽  
Habitat Characteristics ◽  
Home Ranges ◽  
Nothofagus Pumilio ◽  
Old Growth ◽  
Forest Patches ◽  
Argentine Patagonia ◽  
Old Growth Forest

The Magellanic Woodpecker (Campephilus magellanicus (King, 1827)) is a large, vulnerable species exhibiting geographic range retraction. We analyzed the size and location of forest areas used by these woodpeckers in consecutive years (2010–2012), as related to habitat characteristics, in an old-growth lenga (Nothofagus pumilio (Poepp et Endl.) Krasser) forest of Argentine Patagonia. Woodpeckers were tracked during the postbreeding season, and forest features were evaluated in plots within territories. Woodpecker density was 1.01 territories·100 ha–1. The resident population apparently saturates the forest available in the study site; hence, territorial disputes were frequent between all pairs of adjacent families. Families used 39.3 ± 13.6 ha during the postreproductive season and 63.2 ± 12.3 ha across the three seasons, with interannual variability in both location and size of the areas used. Abundances of large live trees and of coarse woody debris were correlated with smaller, presumably high-quality, home ranges. Other forest attributes that are often important in woodpecker habitat (e.g., snag density) had little relationship with home-range size, but the high availability of resources in old-growth forests may mask their potential importance in a poorer quality habitat. Our results show that Magellanic Woodpecker family groups require a minimum of 100 ha in old-growth forest habitat; thus, forest patches in less favourable forest conditions (e.g., younger, managed, fragmented, mixed forests) should probably be much larger to support a resident pair or family. This habitat size would be a provisional minimum threshold to be used in management decisions involving the forests of Patagonia until alternative figures are derived from studies across multiple forest types.

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