The effect of supplementary food on home range of the southern brown bandicoot,Isoodon obesulus (Marsupialia: Peramelidae)

The study investigated the relationship between home range and food abundance in a population of the southern brown bandicoot. Isoodon obesulus, in Western Australia. Home range areas were estimated seven times between 1986 and 1988 by live-trapping, spool-and-line devices and fluorescent pigment tracking. The abundance of invertebrate food was measured simultaneously by placing pitfall traps within the home ranges of individual animals, and by sampling invertebrates in topsoil and litter. Home range areas tended to be negatively correlated with food abundance, especially in the autumn and winter of 1986 and 1987. The influence of food on home range was investigated further in September 1988 by providing eight individual I. obesulus with a supplementary food mixture. Contrary to expectation, the added food caused an increase in home range area, home range overlap and displacement, as well as an influx of new individuals to food stations. In contrast, home range parameters in control (non-fed) individuals changed little during the experiment. The shuffling of home ranges due to feeding suggests that the home range system of I. obesulus is relatively flexible, with individuals monitoring and exploiting resources in an opportunistic manner. In contrast to previous studies, we found no evidence that I. obesulus was territorial. We speculate that individuals may be territorial at low population density if resources are defendable and intruder pressure is low, but occupy overlapping ranges if population density is high.     

Home range and movements of arctic foxes Alopex lagopus in Svalbard

Summary Movements and home ranges of arctic foxes Alopex lagopus were studied in two regions of Svalbard by means of radio tracking (n= 17), ear tagging (n= 192) and visual observations. The movements of radio collared foxes were highly variable, and most foxes roamed over wide areas at least during periods of the year. Home range size was estimated for 11 foxes when more stationary and for three other less stationary foxes, and were in the range 5–120km². During non-stationary periods several foxes roamed over areas 500–1000 km² or more. These movements may more correctly be classified as nomadic, and should not be termed home ranges. Only 3 of 12 radio collarec. foxes that disappeared from an area, returned later. Seven of the 17 foxes were relocated to the same area in more than one season. Overlap of home ranges was extensive, even more so when a number of non-tagged foxes in the regions were included. The heavier juveniles and adults were more sedentary than those of weight lower than median.     

The home range of ship rats (Rattus rattus) in beech forest in the Eglinton Valley,Fiordland, New Zealand: A pilot study

Abstract

Three male and two female ship rats (Rattus rattus) were radio‐tagged and tracked in beech (Nothofagus) forest in the Eglinton Valley, Fiordland, New Zealand over two field periods in 1996 and 2000. The home range of each animal was calculated using the minimum convex polygon method. Ranges of three male rats were 7.5, 9.1, and 11.4 ha whereas those of the female rats were 0.89 and 0.27 ha. The home ranges recorded for male rats were considerably larger than those reported from other studies in non‐beech forest. Ship rats are important predators of forest birds, and home range information could be used to provide a guide for trap or bait station spacing in beech forests. To carry out rat control in beech forests effectively, further studies are needed to determine if the results of this pilot study are typical, and if home ranges of ship rats change with season, or at various stages of the beech mast cycle.     

Home ranges of raccoon dogs (<Emphasis Type="Italic">Nyctereutes procyonoides</Emphasis>, Gray, 1834) in Southern Brandenburg,Germany

The raccoon dog Nyctereutes procyonoides, a medium-sized canid, is a representative of the East Asian fauna and has been introduced to Europe during the years 1928–1953. Today, this alien carnivore is a widespread species in Eastern Europe, Finland and Germany. In our study, we determined home range sizes of raccoon dogs in an agricultural landscape in Northeast Germany between 2001 and 2004 by very high frequency radio tracking. Those data are useful for estimation of predator densities in respect to conservation of biodiversity and also to develop models for disease and parasite transmission. Yearly average home range sizes were calculated as 95% fixed kernel: 1.83 km² ± 1.54 and as 50% fixed kernel (=core areas): 0.50 km² ± 0.49. We documented seasonal differences in home range sizes as well as overlapping of home ranges from 0.65% up to 67%. Some individuals’ home ranges recorded during the same season showed a clear shifting between different years. Abandoned badger dens, located in the core areas of raccoon dogs home ranges, were important during the whole year and particularly used in the winter period. Therefore, distribution of those dens had some influence on the spatial distribution of raccoon dogs in the study area. Based on mean annual home range size, we estimated the mean local population density during winter as 1.1 individuals per square kilometre and during summer as 4.90 individuals per square kilometre.     

Use of space and home range characteristics of Lepilemur mittermeieri,an endangered sportive lemur endemic to the Ampasindava peninsula,north‐west Madagascar

Lepilemur mittermeieri, a little‐studied sportive lemur of north‐west Madagascar, endemic to the Ampasindava Peninsula, faces habitat loss through forest degradation and rapid fragmentation. Understanding its habitat requirement is the first step toward preservation of this threatened forest‐dependent species. In this study, we gathered data on the use of space and home range characteristics of L. mittermeieri. We studied individuals from early March to the end of June 2015 and 2016, in three sites of the Ampasindava peninsula. We radio‐tracked 15 individuals to obtain detailed information on the size and location of home ranges (around 450 hr of tracking). Direct observation and morphometric measurements provided additional data sets. Both kernel density estimation (KDE) and minimum convex polygon (MCP) methods yielded similar home range sizes (an average of 2.01 ha with KDE method and 1.96 ha with MCP method). We did not find differences in home range size between males and females, with respect to forest type or proximity to the forest edge. Home ranges overlapped and individuals showed low levels of territoriality. We highlighted a sexually‐dimorphic trait: males have longer upper canine than females. Our results constitute the first set of ecological information on Lepilemur mittermeieri and could be the basis for a conservation strategy for this endangered species with a very small distribution area.     

Social organization of Galagos in Kenyan coastal forests: II. Galago garnettii

The social organization of Galago garnettii was studied for the first time and the study included data from two different sites in the coastal forests of Kenya. A combination of mark-recapture and radio-tracking techniques was used to investigate patterns of inter- and intrasexual home range overlap. Patterns of range use were established by radio tracking focal individuals. Adult females of different ages shared highly overlapping ranges, while like-aged females showed little range overlap. Females matured and had their first infants in their natal ranges. Adult males' ranges were larger than those of females and overlapped them extensively. Resident adult males showed little range overlap with each other, unless they were of different ages. Turnover of males was frequent in both populations. Males probably dispersed from their natal ranges. Adults rarely slept together. The social organization of G. garnettii is relatively similar to that of the closely related G. crassicaudatus of southern Africa but contrasts with that of its sympatric congener, G. zanzibaricus. The differences and similarities between these three species are discussed in relation to diet and body size.     

Space use and site fidelity of wintering whooping cranes on the Texas Gulf Coast

The Aransas-Wood Buffalo population (the only non-reintroduced, migratory population) of endangered whooping cranes (Grus americana) overwinters along the Texas Gulf Coast, USA. Understanding whooping crane space use on the wintering grounds reveals essential aspects of this species' ecology, which subsequently assists with conservation. Using global positioning system telemetry data from marked whooping cranes during 2009–2017, we fit continuous-time stochastic process models to describe movement and home range using autocorrelated kernel density estimation (AKDE) and explored variation in home range size in relation to age, sex, reproductive status, and drought conditions. We used the Bhattacharyya coefficient of overlap and distance between home range centroids to quantify site fidelity. We examined the effects of time between winter home ranges and the sex of the crane on site fidelity using Bayesian mixed-effects beta regression. Winter whooping crane 95% AKDE home range size averaged 30.1 ± 45.2 (SD) km² (median = 14.3, range = 1.1–308.6). Home ranges of sub-adult females were approximately 2 times larger than those of sub-adult males or families. As drought worsened, home ranges typically expanded. Between consecutive years, the home ranges of an adult crane exhibited 68 ± 31% overlap (site fidelity), but fidelity to winter sites declined in subsequent winters. The overlap of adult home ranges with the nearest unrelated family averaged 33 ± 28%. As a whooping crane aged, overlap with its winter home range as a juvenile declined, regardless of sex. By 4 years of age, a whooping crane had approximately 14 ± 28% overlap with its juvenile winter home range. Limited evidence suggested male whooping cranes return to within 2 km of their juvenile home range by their fifth winter. Previous data obtained from aerial surveys led ecologists to assume that whooping crane families normally used small areas (~2 km²) and expressed persistent site fidelity. Our analyses showed <8% of families had home ranges ≤2 km², with the average area 15 times greater, and waning site fidelity over time. Our work represents an analysis of whooping crane home ranges for this population, identifying past misconceptions of winter space use and resulting in better estimates of space requirements for future conservation efforts.     

Activity and movement patterns of Octopus dofleini

Four individual Octopus dofleini were followed over a fifteen day period in their underwater habitat by sonic tracking. Octopuses had small home ranges (250 m²maximum) which were stable over the two weeks of observation. These ranges overlapped those of other octopuses extensively, and animals did not keep a constant distance from one another, which suggests they were solitary and non‐social. Activity was slightly higher at night, and was not correlated with changes in other environmental variables. The O. dofleini made frequent short hunting trips (mode 0.5 hours), tending to have more and longer excursions at night. Octopuses are predators who appear to have flexible activity and, in the short term, restricted home range areas.     

Home range and territory of the Sardinian Warbler Sylvia melanocephala in Mediterranean shrubland

Capsule Singing territories were well separated.

Aims To examine the spatial distribution of Sardinian Warbler males during the breeding period in Mediterranean shrubland and, specifically, their territories, home ranges and spatial overlaps.

Methods We studied a 12-ha plot of Mediterranean shrubland in the 1997 to 1999 breeding seasons. Sardinian Warblers were captured using mist-nets, colour-ringed and their territories mapped. In 1999, seven breeding males were radiotracked in order to map home ranges.

Results The Sardinian Warbler had an average of 7.3 breeding pairs/10 ha in the study plot. The mean territory size was 8779 m² and the mean home range was 22 321 m². A positive relationship was found between the area of the home range and singing territory. Home ranges of males born in 1998 were about half the size of those of the oldest males. Paired males who moved with a female had smaller home ranges than those that were either unpaired or whose mate was incubating. The degree of home range overlap was high with some overlap between neighbouring territories. The estimate of home range area increased by 10% when the information generated by a mapping method was added and the estimated territory area increased by 31% when data generated by radiotracking were added. Transmitters remained attached to birds for an average of 9.63 ± 3.46 days (mean ± se).

Conclusions Singing territories were segregated to a considerable degree. In contrast, the wide overlaps among home ranges was best explained by the presence of food resources that the males exploit at the same time and also by the search for extra-pair copulation in nearby territories. We consider radiotracking in this species to be feasible and valid, with no evidence of negative effects on activity levels, weight or mortality.     

Ecological consequences of a group fission event in the Tana River mangabey (Cercocebus galeritus)

A group of Tana River mangabeys Cercocebus galeritus studied in 2000–2001 fissioned into two daughter groups in 2004, the first reported case of fission in Cercocebus. Data were collected on each daughter group in 2005–2006 to investigate how the groups divided the parent group's range, the quality of habitat used by each group, and if fruit abundance was correlated with the spatial relationships between the groups. Six days of ranging data were collected each month and input into ArcView GIS 3.3 to measure home ranges and core areas. Phenological data were collected from nine important food species. Habitat quality was measured by counting all reproductive‐sized individuals of those nine food species in the ranges. The daughter groups shared the parent group's home range and core area, although the larger group used more of those areas than the smaller group. The two groups got equal quality home ranges and core areas as measured by per capita food trees, but the larger group had access to a larger and richer exclusive area. Proximity of the groups to each other was not correlated with fruit abundance. This study contributes to the small body of literature that addresses ecological consequences of primate group fission.     

Range use of the forest chimpanzees of Kibale: Implications for the understanding of chimpanzee social organization

We contrast the range use patterns of male and female chimpanzees (Pan troglodytes) based on repeated sightings over three years of 19 individuals in the Kanyawara community of Kibale Forest Reserve, Uganda. Depending on how home range size was calculated, male chimpanzees used an area that was 1.5 to 2 times greater than that of females. There was no difference between the sexes in whether their home ranges were used in a clumped or uniform fashion. However, males were more likely to be seen in boundary areas than females. These results are discussed in light of previously proposed models of chimpanzee social organization. It is concluded that the scenario in which females have smaller core areas within the defended home range of the males is most strongly supported by the range use patterns observed in Kibale chimpanzees. © 1993 Wiley-Liss, Inc.     

Passive acoustic telemetry reveals highly variable home range and movement patterns among unicornfish within a marine reserve

Marine reserves are the primary management tool for Guam’s reef fish fishery. While a build-up of fish biomass has occurred inside reserve boundaries, it is unknown whether reserve size matches the scale of movement of target species. Using passive acoustic telemetry, we quantified movement patterns and home range size of two heavily exploited unicornfish Naso unicornis and Naso lituratus. Fifteen fish (N. unicornis: n = 7; N. lituratus: n = 4 male, n = 4 female) were fitted with internal acoustic tags and tracked continuously over four months within a remote acoustic receiver array located in a decade-old marine reserve. This approach provided robust estimates of unicornfish movement patterns and home range size. The mean home range of 3.2 ha for N. unicornis was almost ten times larger than that previously recorded from a three-week tracking study of the species in Hawaii. While N. lituratus were smaller in body size, their mean home range (6.8 ha) was over twice that of N. unicornis. Both species displayed strong site fidelity, particularly during nocturnal and crepuscular periods. Although there was some overlap, individual movement patterns and home range size were highly variable within species and between sexes. N. unicornis home range increased with body size, and only the three largest fish home ranges extended into the deeper outer reef slope beyond the shallow reef flat. Both Naso species favoured habitat dominated by corals. Some individuals made predictable daily crepuscular migrations between different locations or habitat types. There was no evidence of significant spillover from the marine reserve into adjacent fished areas. Strong site fidelity coupled with negligible spillover suggests that small-scale reserves, with natural habitat boundaries to emigration, are effective in protecting localized unicornfish populations.     

Resource distribution influences mating system in the bobuck (<Emphasis Type="Italic">Trichosurus cunninghami</Emphasis>: Marsupialia)

Mammalian mating systems are thought to be shaped by the spatial distribution and abundance of key resources, which in turn influence the spacing behaviour of individuals. In particular, female home range size is predicted to reflect the availability of key resources. We documented the availability and distribution of food and shelter resources for two neighbouring populations of bobucks, or mountain brushtail possums, Trichosurus cunninghami, that were characterised by different mating systems: our “forest population” was socially monogamous, whereas the “roadside population” was polygynous. Both silver wattle, Acacia dealbata, the main food resource for bobucks, and den-trees, which provided shelter, occurred at significantly higher density at the roadside site. The pattern of distribution of these two resources also differed between the sites. Both food and den-trees were scattered evenly throughout the roadside habitat. In contrast, den-trees were located predominantly at one end of the forest site, while silver wattle trees were located at the other. There was no significant difference in the amount of silver wattle, or in the number of den-trees, located within the home ranges of individual females at the two sites. However, forest females had home ranges, on average, almost three times the size of those of roadside females. At the roadside site, the size of female home ranges varied inversely with the density of silver wattle, indicating that these females ranged over as large an area as necessary to gain access to sufficient silver wattle trees. There was no such relationship among forest females. These populations provide a clear example of resource distribution determining female home range size. This influenced the number of female home ranges a male’s home range overlapped with, which in turn determined the mating system. Such clear links between resource availability and mating system have not previously been established in a marsupial.     

Long-term Site Fidelity and Individual Home Range Shifts in <Emphasis Type="Italic">Lophocebus albigena</Emphasis>

We investigated long-term site fidelity of gray-cheeked mangabey (Lophocebus albigena) groups in Kibale National Park, Uganda. Concurrently, we monitored shifts in home range by individual females and subadult and adult males. We documented home range stability by calculating the area of overlap in successive years, and by recording the drift of each group’s monthly centroid from its initial location. Home ranges remained stable for 3 of our 4 groups (overlap over 10 yr >60%). Core areas were more labile, but group centroids drifted an average of only 530 m over the entire decade. Deviations from site fidelity were associated with dispersal or group fission. During natal dispersal, subadult males expanded their home ranges over many months, settling ≤4 home ranges away. Adult males, in contrast, typically dispersed within a few days to an adjacent group in an area of home range overlap. Adult males made solitary forays, but nearly always into areas used by their current group or by a group to which they had previously belonged. After secondary dispersal, they expanded their ranging in the company of their new group, apparently without prior solitary exploration of the new area. Some females also participated in home range shifts. Females shifted home ranges only within social groups, in association with temporary or permanent group splits. Our observations raise the possibility that male mangabeys use a finder-joiner mechanism when moving into new home ranges during secondary dispersal. Similarly, females might learn new resource locations from male immigrants before or during group fission.     

Home range and ranging pattern in the slender loris(Loris tardigradus lydekkerianus)

The home range and ranging pattern of the slender loris (Loris tardigradus lydekkerianus) was studied for 21 months in a scrub jungle in Dindigul, Tamil Nadu, south India. Sixteen individuals were observed for a total of 2261 hours. Home ranges were measured for eight adult individuals and eight juvenile and subadult individuals. Males had significantly larger home ranges than the females, and home range size increased post-weaning. The ranging patterns involved minimal female intrasexual overlap, large male intrasexual overlap and large intersexual range overlap.     

Home range use and the exploitation of gum in the marmosetCallithrix jacchus jacchus

Three wild groups of common marmoset, Callithrix jacchus jacchus,in north-east Brazil, of approximately similar size, had home ranges between 2.5 and 6.5 ha. But their core areas were similar in size between 1.0 and 1.5 ha, with a monthly area of heavy use between 1.1 and 1.6 ha. The groups were selective in the use of their home ranges, even though they were small: they used some areas heavily and others lightly. The core areas had higher densities of trees that produced gum exudates than did other parts of the home ranges. Our data suggest that a group of marmosets in this habitat may require a minimum of about 50 gum trees in its home range at a minimum density of about 50 trees/ha. In addition, the animals require suitable trees in which to sleep. We suggest that patches of forest with these desirable properties remain relatively fixed in size and location over the years and that individual animals are constantly in flux between them.     

Effect of mast production on home range use of Japanese black bears

Although bears may expand their home ranges in times of low food availability, it is unclear what mechanisms directly affect home range extension in times of low mast production in Japanese forests. To clarify the relationship between home range utilization by Japanese black bears (Ursus thibetanus) and abundance and distribution of mast production, we collected data on habitat use from 13 bears (6 M and 7 F) fitted with Global Positioning System (GPS) collars equipped with activity sensors in the Ashio-Nikko Mountains on the eastern part of Honshu Island, Japan, during 2006–2008. We also collected data on mast production by 5 Fagaceae species. We categorized each fall as either poor (2006) or relatively-good (2007 and 2008) based on mast production. Bears used small patches in their large home ranges and the distances between core areas increased in the fall of 2006, when the mast of Japanese oak (Quercus crispula) were poorly distributed. Our findings suggest that localized patches of Japanese oak are the staple food for bears in our study area, even in poor mast years. However, in the fall of 2006, we also found that bears moved to lower elevations, relative to 2007 and 2008, in search of alternative foods (e.g., Konara oak [Q. serrata] and Japanese chestnut [Castanea crenata]), which were mostly at lower elevations and produced mast consistently over the study period. Our results suggest that dispersion and elevational distribution of mast-producing trees affect bear habitat use in fall, as well as amount of mast. © 2011 The Wildlife Society.     

Effects of Food Availability on Space and Refuge Use by a Neotropical Scatterhoarding Rodent

Animals that rely on refuges for safety can theoretically increase their foraging area without simultaneously increasing predation risk and travel costs by using more refuges. The key prediction of this theory, a negative correlation between food abundance, home range size and the number of refuges used, has never been empirically tested. We determined how home range size and refuge use by the Central American agouti (Dasyprocta punctata) varied across a gradient of abundance of the agoutis' principal food source: seeds and fruits of the palm Astrocaryum standleyanum. We used both manual and automated radio telemetry to measure space use of 11 agoutis during 2 mo of the Astrocaryum fruiting season, and of another set of 10 agoutis during 6 mo in which the animals largely relied on cached Astrocaryum seeds. We found that agoutis living in areas of lower food density had larger home ranges, and that all individuals used multiple refuges. The number of refuges, however, was not correlated with home range size. Consequently, agoutis that had larger home ranges roamed farther from their refuges. These results suggest that agoutis increase their home range size in response to food scarcity at the cost of their safety.     

Home ranges in red fox: territoriality diminishes with increasing area

Red foxVulpes vulpes (Linnaeus, 1758) are generally regarded as strictly territorial animals, inhabiting distinct and well-separated ranges. The home ranges of these predators can vary in size from a few dozen hectares to as much as 20–30 km². Because it seemed impossible that foxes could defend areas so different in size with the same intensity, the published data were analysed in order to see how changes in home range size could affect the following parameters: home range overlap, the area visited daily and the distance travelled by animals during 24 h. It was found that the overlap between fox families (groups) occupying large ranges was much greater than between foxes living in small ranges. The ratio of the area visited daily to the seasonal home range size was greater in small ranges than in large ones. No significant correlation was found between the mean distance moved daily and home range size (r = −0.118,p = 0.75). These results suggest different patterns of the use of space and differences in territorial defence by red foxes inhabiting large and small ranges. The implications of home range overlap and intensity of contacts between foxes occupying neighbouring ranges for the spread of disease are discussed. The significant overlap between large ranges found in this paper is discussed in the light of Andrzejewski’s (2002) home range concept.

     

Social system of an inshore stock of the red hind grouper,Epinephelus guttatus (Pisces: Serranidae)

Synopsis According to sex allocation theory, the decision by a female in protogynous fish species to change sex or not should be influenced by, among other things, the mating sex ratio during spawning periods and/or by factors that vary directly with the spawning sex ratio, such as relative rates of behavioral interaction with males and females outside of spawning periods. In groupers that only spawn during a few weeks of the year in large aggregations, individuals must assess the relative value of changing sex or not entirely within the aggregation unless the social system during the remainder of the year provides a behavioral equivalent of the mating sex ratio. Fifty-five individuals of the red hind,Epinephelus guttatus, were tagged and repeatedly located during a 152-day period within a 100 × 100 m grid on a shallow forereef off southwestern Puerto Rico. The home ranges of 22 tagged individuals sighted 10 or more times were 112–5636 m² in area. Individual home ranges overlapped with the home ranges of 1–18 other individuals. Home ranges of small fish were not clustered within the borders of the home range of larger fish, i.e. fish did not form spatially defined social units. At the end of the study, 31 tagged individuals remained on the grid together with five newly sighted fish. All 36 individuals proved on histological examination to be females similar in size to females in the spawning aggregation of the following year. The sex ratio of this all-female inshore stock differed significantly from the sex ratio of that spawning aggregation. Hence, information predicting the reproductive value of a sex change is not available to females in the inshore stock during nonspawning months.