A review of home-range studies on Australian terrestrial vertebrates: adequacy of studies, testing of hypotheses, and relevance to conservation and international studies

2015 ◽  
Vol 63 (2) ◽  
pp. 136 ◽  
Author(s):  
Ross L. Goldingay

Describing the spatial requirements of animals is central to understanding their ecology and conservation needs. I reviewed 115 studies describing the home ranges of Australian terrestrial vertebrates that were published during 2001–12. Understanding the features that characterise best practice can guide future studies. I aimed to: evaluate the adequacy of these studies, examine the use of current analysis techniques, examine the application of home-range knowledge to species’ management, and examine hypotheses that seek to explain the size and location of home ranges. The reviewed studies were unevenly distributed across taxa with a majority (68%) involving mammals compared with birds (12%), reptiles (19%) and frogs (1%). Many studies had various shortcomings, suggesting that they had not fully described home ranges; many (41%) involved 10 or fewer individuals, ≤50 locations per individual (44%), and spanned periods of ≤3 months (46%). Studies of short duration risk underestimating home-range area and overlooking seasonal habitat use. Global positioning system telemetry was used in 10% of Australian studies. Many were also of short duration. Despite frequent criticism in the literature, the Minimum Convex Polygon was the most frequently used home-range estimator (84% of studies), followed by the Fixed Kernel (45% of studies). Applying knowledge of home ranges appears to be underappreciated, with only 39% of studies explicitly aiming to address management or conservation issues. Only three studies tested hypotheses that may explain home-range characteristics. Resource (food and shelter) distribution and, in one case, its heterogeneity, shaped home-range characteristics. I found that most studies use the term ‘home range’ in an indiscriminate way. Only 11% of studies within the international literature used qualifying terms (e.g. seasonal, annual). Tracking period is shown to influence home-range estimates. Therefore, I recommend that qualifying terms be used more frequently to avoid confusion when referring to animal home ranges.


2010 ◽  
Vol 32 (1) ◽  
pp. 23 ◽  
Author(s):  
Alan Robley ◽  
Andrew Gormley ◽  
David M. Forsyth ◽  
Alan N. Wilton ◽  
Danielle Stephens

To investigate movements and habitat selection by wild dogs we attached satellite-linked global positioning system (GPS) units to nine wild dogs (Canis lupus dingo and Canis lupus familiaris) captured in eastern Victoria in summer 2007. Units estimated locations at 30-min intervals for the first six months and then at 480-min intervals for six more months. DNA testing revealed all these wild dogs to be related. Home ranges of males were almost three times larger than those of females (males: 124.3 km2 ± 56.3, n = 4; females: 45.2 km2 ± 17.3, n = 5) and both sexes preferred subalpine grassland, shrub or woodland at the landscape and home-range scales. Wild dogs were recorded more often than expected within 25 m of roads and less often than expected within 25 m of watercourses. Wild dogs displayed higher-velocity movements with shallow turning angles (generally forwards) that connected spatial and temporal clusters comprising slower-velocity, shorter, and sharper turning movements. One wild dog travelled 230 km in 9 days before returning to its home range and another travelled 105 km in 87 days. The home-range sizes reported in this study are much larger than previously reported in south-eastern Australia. This finding, together with previous studies, suggests that the spatial scale at which wild dog management occurs needs to be reconsidered.



2010 ◽  
Vol 32 (2) ◽  
pp. 183 ◽  
Author(s):  
Ross L. Goldingay ◽  
David J. Sharpe ◽  
Matt D. J. Dobson

The home-range area of animals may vary geographically and in response to habitat quality. We investigated the size of squirrel glider (Petaurus norfolcensis) home ranges near Brisbane, Queensland, and at Tea Gardens on the central coast of New South Wales. Habitat at both sites had been partially cleared and had been subjected to grazing for several decades. Twelve gliders were tracked over an average of 3.5 months in Brisbane. The fixed kernel (FK95%) home-range estimate averaged 4.6 ± 0.7 (s.e.) ha while the minimum convex polygon (MCP100%) averaged 6.7 ± 1.5 ha. Six gliders were tracked over 1 month at Tea Gardens. The FK95% home-range estimate averaged 14.8 ± 2.4 ha while the MCP100% averaged 13.3 ± 3.1 ha. The Tea Gardens values are derived from relatively short periods and are likely to underestimate the areas used. This study demonstrates that home-range size can vary substantially in the squirrel glider. This has implications for understanding how this species responds to variation in habitat quality and highlights the need for site-specific studies to inform aspects of management.



2007 ◽  
Vol 34 (3) ◽  
pp. 177 ◽  
Author(s):  
Robyn F. Wilson ◽  
Helene Marsh ◽  
John Winter

Roads and powerline corridors destroy canopy connectivity in the rainforest of north-east Australia. We tested the hypotheses that linear barriers affect (a) the alignment of home ranges, (b) use of habitat either side of linear barriers, and (c) the crossing of them by the strictly arboreal lemuroid ringtail possum (Hemibelideus lemuroides), which is known to be vulnerable to habitat fragmentation. Radio-tracking and a translocation experiment were conducted at a narrow 7-m-wide road and an 80-m-wide powerline. Homes ranges of lemuroid ringtails ranged from 0.15 to 1.67 ha (minimum convex polygon) and were aligned with the road but not powerline corridors. When lemuroid ringtails were experimentally translocated, wider canopy clearings over roads reduced their capacity to return to their original home range, and the powerline corridor was a nearly insurmountable barrier. No possums were observed crossing roads or the powerline corridor at ground level or residing in the intervening matrix, indicating that loss of canopy connectivity has a negative impact on their movements.



2010 ◽  
Vol 75 (658) ◽  
pp. 2809-2815 ◽  
Author(s):  
Daisuke MATSUSHITA ◽  
Minami NAGATA ◽  
Junzo MUNEMOTO ◽  
Tomoyo NAKAMURA


1996 ◽  
Vol 23 (6) ◽  
pp. 711 ◽  
Author(s):  
G Saunders ◽  
B Kay

The movements of a subalpine population of feral pigs were examined at Kosciusko National Park in southeastern New South Wales. Sufficient data were collected to estimate the home-range area of 20 pigs on the basis of 782 telemetry and trap locations. Mean (+/- s.d.) home-range size (minimum convex polygon method) for males (35.0 t 22.2 km*2) was significantly greater than that for females (1 1.1 +/- 5.2 km*2). Use of capture-recapture distances to estimate home-range size was considered inappropriate. A test for nomadism suggests that, although home ranges of pigs in this environment were larger than those reported for other pigs in Australia, the pigs were essentially sedentary. Management implications for this population are discussed.



2014 ◽  
Vol 36 (1) ◽  
pp. 74 ◽  
Author(s):  
Ross L. Goldingay ◽  
Barbara Dobner

Conserving wildlife within urban areas requires knowledge of habitat requirements and population processes, and the management of threatening factors. The koala (Phascolarctos cinereus) is one species that is adversely affected by urban development. Sick and injured koalas in the Lismore urban area are regularly taken into care. We radio-tracked koalas released from care in order to estimate home-range areas and to determine their fate. Koalas were tracked for periods of 90–742 days; 7 of 10 survived for a period of at least one year. Home ranges defined by the minimum convex polygon (MCP100%) were large (mean ± s.e. = 37.4 ± 8.2 ha). Analysis using the 95% Fixed Kernel revealed home-range areas of 8.0 ± 1.7 ha. Analysis of the habitat composition of each MCP home range showed that they included 4.3 ± 0.9 ha of primary habitat (dominated by their primary food trees). These home ranges contained 27.6 ± 6.8 ha of non-habitat (cleared or developed land). Koalas crossed roads within their home ranges at least 5–53 times; one crossed the Bruxner Highway near a roundabout at least 32 times over his 2-year tracking period. Future management should include strategic food tree planting that enhances habitat connectivity and minimises the risk of car strike or dog attack.



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.



The Auk ◽  
2019 ◽  
Vol 136 (2) ◽  
Author(s):  
Csaba Moskát ◽  
Miklós Bán ◽  
Attila Fülöp ◽  
Judit Bereczki ◽  
Márk E Hauber

Abstract Obligate brood parasitic birds have evolved a rare avian strategy for reproduction by laying eggs in the nests of other species. In doing so, their breeding ranges, but not necessarily their foraging habitats, have become intimately related to the nesting territories of their hosts. We studied home range sizes and distribution patterns in Common Cuckoos (Cuculus canorus) on their breeding grounds in central Hungary, where cuckoos parasitize only Great Reed Warblers (Acrocephalus arundinaceus) in channel-side reed-beds at a high frequency (>50%). The geographic coordinates of tagged cuckoos were monitored by high-precision, remotely downloadable non-Platform Terminal Transmitter global positioning system (GPS) loggers, attached to 9 females and 6 males. Our results revealed bimodal use of habitat patches: (1) the home ranges of male and female cuckoos were packed densely along the channels where the hosts breed, and their distribution maps had high overlaps between sexes; (2) ~71% of cuckoos also visited nearby woodland patches, presumably for foraging, where the host species was not present. The size of cuckoo home ranges varied to an unusually great extent: 0.3–185 km2 as calculated by the minimum convex polygon method (85%), or 1–17 km2 when calculated by the more suitable kernel density estimation (KDE) method (Utilization Distribution 85%) for patchy habitats. Male and female cuckoos had similar home range sizes as estimated by the KDE method, consisting of 1–4 areas within the 2 habitat types of channel reed-beds and woodlands. No preference was revealed for night roosting locations between the 2 habitats or sexes. Female cuckoos were more likely to use reed-beds in the afternoons, when females parasitize host nests. Remote downloadable GPS methods offer an effective way of tracking cuckoos across large areas, but the estimation of home range sizes requires caution due to this species’ patchy and disconnected habitat use.



2010 ◽  
Vol 88 (10) ◽  
pp. 968-976 ◽  
Author(s):  
Ryan K. Brook

I examined the home range and habitat selection of 146 radio-collared female elk ( Cervus elaphus L., 1758) from 2002 to 2005 during the calving period (15 May to 24 June). I determined the proportion of home ranges of parturient cow elk during the calving period and the proportion of birthing sites of elk that were in either forested protected areas or the adjacent fragmented agriculture-dominated matrix in southwestern Manitoba, Canada. Overall, 73% of the minimum convex polygon home ranges were entirely within a protected area, 6% were only on farmland, and 21% included both. Home ranges including farmland and protected area (mean = 17.9 km2) were 3.8 times larger than those entirely inside a protected area (mean = 4.7 km2) or only on farmland (mean = 4.5 km2) (U = –2.79, P = 0.005). Female elk remaining solely in protected areas selected deciduous and mixedwood forest, marsh and fen, and water at the scale of the home range. Elk exclusively on farmland selected forage crops only. At the scale of the birthing site, females on farmland and those in protected areas selected only deciduous forest, and both types avoided agricultural cropland and marsh and fen. Identification of calving habitat will allow resource managers to manage bovine tuberculosis in the population more effectively.



1995 ◽  
Vol 22 (3) ◽  
pp. 299 ◽  
Author(s):  
V Mirmovitch

Feral cats were studied for 10 months in a residential area in Jerusalem and their spatial distribution compared during two 1-month periods, the first in the autumn prior to the mating season and the second during the mating season (winter). Cat locations were recorded by direct observations, and home-range sizes were calculated with the minimum convex polygon method. No significant change in home-range size of adult males or females was found between the 2 periods. Young males expanded their home ranges considerably during their first mating season. Home ranges of males were significantly larger than those of females in both periods (0.56 and 0.30 ha, respectively, in autumn; 0.75 and 0.27 ha in winter). The home ranges of both sexes overlapped considerably with individuals of the same sex. Overlap among home ranges of females indicated a group pattern. High overlap (80%) was found among females that fed from the same set of garbage bins with similar frequency. Lower overlap (20%) was found between individual females that shared only a subset of their food resources and used it with different frequency. It is suggested that the distribution of food patches (garbage bins), the amount of food available and the rate of food renewal determined the cats' spatial organisation.



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