Spatial organization of leopards Panthera pardus in Taï National Park, Ivory Coast: is rainforest habitat a 'tropical haven'?

Between June 1992 and July 1994, two female leopards and one male were radio-tracked. Regular locations of the leopards, the use of a phototrap, and spoor data, provided the first detailed ecological data about this elusive felid in tropical rainforest habitat. The home range of the male was 86 km², those of the two females were 29 km² and 22 km², respectively. One female's home range was fully included within that of the male. Home ranges of neighbouring residents were not exclusive. Population density is estimated at one leopard per 9-14 km². Intraspecific interactions were rare and predominantly involved mating. The large size of the home ranges and a relatively high population density imply large overlap between adjacent resident leopards' ranges. Differences in the leopard's land tenure system between the rainforest and the savanna are discussed. Doubt is cast on the validity of the often-quoted estimate of one leopard per 1 km² in tropical rainforest habitat.     

Intraspecific interactions in a high‐density leopard population

Although less studied than interspecific interactions, interactions among members of the same species can influence space use and temporal activity. Using techniques commonly applied to the analysis of interspecific interactions—multispecies occupancy modeling and the analysis of temporal activity patterns—we studied intraspecific interactions within a high‐density population of Persian leopards (Panthera pardus saxicolor) in Tandoureh National Park, northeastern Iran. Using camera‐trap data, we investigated spatiotemporal interactions between male leopards, lone female leopards, and families (cubs/females with cubs). While we hypothesized that male and female leopards would display different temporal activity patterns, we did not predict spatial avoidance between these groups. We also predicted that leopard families would exhibit spatiotemporal avoidance from male leopards due to the risk of infanticide. Contrary to our expectations, we did not find any evidence for spatial or temporal avoidance between leopard families and adult male leopards. Male and lone female leopards exhibited positive pairwise co‐occurrence, consistent with reports of high overlap between male and female leopard home ranges. While a high level of overlap in temporal activity patterns was found between males/lone females and males/families, there was evidence for variation in the proportion of time each leopard group was active in particular periods of the diel cycle. Male leopards showed cathemeral activity, while lone females and families were more active during daylight hours. The application of these techniques to interactions within a species has improved understanding of the ecology and behavior of this endangered solitary carnivore.     

Home-range use, activity, and density of caracal in relation to prey density

Two male and three female caracal Felis caracal were radio-tracked over a 1-year period in arid shrub on the west coast of South Africa, by day and night over at least 130 days for each caracal, and uninterrupted for up to 120 h at a time. These results, on short-term use of space, were related to concurrent availability of prey. The use by caracal of specific plant communities showed a significant positive correlation to prey biomass of rodents. Males had much larger home-ranges (26.9±0.75 km²) than females (7.39±1.68 km²). Male home-ranges overlapped completely with those of females, whereas female ranges overlapped between 0 and 19%. Caracal were active by night and day; onset of activity was affected more by ambient temperature (T_A) than photoperiod. Caracal were active significantly longer on nights colder than 20°C. Females ceased activity at T_A > 20°C, males at T_A > 22°C. Males foraged faster than females (667 vs. 312 m h⁻¹) and moved more than twice the distance of females during an active period. Calculated density of caracal was between 0.23 and 0.47 km⁻².     

Population ecology of the white-nosed coati (Nasua narica) on Barro Colorado Island, Panama

The white-nosed coati, Nasua narica , is a common Neotropical carnivore with a social structure of band-living adult females and solitary adult males. A coati population on Barro Colorado Island, Panama, was studied over a four-year period by mark-recapture, radiotelemetry. and direct observation of habituated individuals. The population density was approximately 51.5 individuals/km² and the sex ratio was 1:1. Band size varied from six to 26 individuals (mean = 15.3) with extensive fluctuation within and between years. Mean foraging group size was smaller (7.2 individuals) than population group size, and fluctuated with food availability, synchronous parturition, and the emigration of mature males. Mean home-range size of six bands was 0.33 km², and ranges of adjacent bands overlapped from 0–66%. One band fissioned during the study; however, the resulting bands did not disperse from the original home range. Seven adult males had a mean home-range size of 0.37 km², each extensively overlapping the home ranges of several other males. Observations of 10 adult males whose natal bands were known indicate that when males disperse they do not simultaneously leave the band's home range. Rather, their home ranges remain within or broadly overlapping those of their natal bands. This dispersal pattern is unusual within the order Carnivora.     

Ecology and behaviour of the Jaguar (Panthers onca) in Belize, Central America

Five adult male Jaguars and a translocated subadult female Jaguar were captured and followed by radio-telemetry in Cockscomb Basin, Belize. One adult male Jaguar, two resident female Jaguars, and a Puma were followed only by their tracks. Radio-collared males maintained overlapping ranges of 28–40 km², while resident females moved in minimum areas of 10 km² within the ranges of individual males. Despite range overlap, evidence of aggression or sign of more than one large cat in the same area simultaneously was uncommon. Such avoidance behaviour suggested some means of communication. Visual marking in the form of faeces and scrapes were found uncovered along roads and trails in areas of overlap between the cats; such marking could have helped in boundary delineation as well as spatial and temporal positioning. Males often remained in small areas of 2·5 km² for up to two weeks, a behaviour made possible by abundant prey. This behaviour may have facilitated avoidance with other Jaguars. Faecal analysis indicated opportunistic feeding on 17 prey species. Armadillo, Paca and brocket deer accounted for 94% of the available terrestrial prey and comprised 70% of the identified prey in the faeces. All Jaguars were primarily nocturnal, though activity varied between animals. The translocated female showed changes in activity patterns when feeding upon cattle. At least one Puma travelled within the ranges of several male Jaguars and appeared to be feeding on smaller prey items. The behavioural and ecological plasticity exhibited by the Jaguars in this study is beneficial for an animal whose habitat is rapidly diminishing.     

Home range and habitat use of wolverines Gulo gulo in Yukon, Canada

Home ranges and habitat use are described for three adult female, one adult male, and one subadult male wolverines in the Kluane Game Sanctuary, Yukon. When long distance excursions are not included, home ranges of wolverines in the Kluane Game Sanctuary were between 76 and 269 km² for females and 209 and 269 km² for males. Habitat use of females was similar to habitat availability. Males used subalpine coniferous habitats more frequently than other habitat types during winter. Although individual variation in the use of forest cover types, aspects, slopes and elevations was apparent, seasonal use did not differ from availability for each sex. Within the 1590 km² study area, three adult males and six adult females were present, corresponding to a density of one resident wolverine 177 km^-2.     

Spatial organization in the Ethiopian wolf Canis simensis: large packs and small stable home ranges

The spatial organization of the rare Ethiopian wolf ( Canis simensis ) was studied in the Afroalpine heathlands of Bale Mountains National Park, southern Ethiopia, between 1988 and 1992. Nineteen animals were radio-tracked, 48 ear-tagged and 64 others recognized by coat patterns and observed directly. Dry season (October—March) home ranges of resident wolves covered between 2 and 15 km². The ranges of adult males were slightly larger than those of females, and subadults' home ranges were slightly smaller than those of adults. The population density of the wolves was correlated with prey biomass. In optimal habitat, wolves lived in packs of 3—13 adults (mean 5.9 wolves > 1year old) containing several close-kin males; adult sex ratio favoured males 1.88: 1 and combined pack home ranges averaged 6.0km². In an area of lower prey productivity, wolves lived in pairs or small groups (mean 2.7), adult sex ratio was 1:1 and home ranges averaged 13.4 km².
Home ranges overlapped extensively (mean 85%) between members of the same pack. Four to seven percent of the population was additionally composed of non-resident females, inhabiting larger ranges (mean 11.1 km²). Home ranges of neighbouring packs were largely discrete, forming a tessellating mosaic of packs occupying all available habitat. Pack home ranges were stable in time, drifting only during major pack readjustment after the disappearance of a pack or significant demographic changes. Ethiopian wolf home ranges were smaller than would be expected for a carnivore of its size and sociality, presumably as a result of the high rodent productivity of the Afroalpine ecosystem.     

Spatial organization and recruitment of lynx (Lynx lynx) in a re-introduced population in the Swiss Jura Mountains

We monitored seven resident (three males and four females) and six dispersing subadult Eurasian lynx from to in a population that was re-introduced to the Swiss Jura Mountains in the early 1970s. Home-range areas of the neighbouring adults were 71–281 km², and significant core areas 34–252 km². Males occupied significantly larger areas than females. Home-range overlap was 9% for neighbouring males and 3%) for females. Core areas of males did touch, but those of females were clearly separated. Each male's home range covered those of one or two females. Population density was 0.94 lynx/100 km² for resident animals. Pre-dispersal mortality was estimated to be 50%. Juveniles dispersed from their mothers' home area at the age of 10 months. Of six monitored subadults. only one survived the first year of independence. Human-caused mortality (traffic accidents. illegal killing) was high. This was also the case among resident adults. This might be a threat to the long-term survival of the reintroduced population.     

Spatial ecology of cheetahs on north-central Namibian farmlands

Knowledge of a species' ranging behaviour is both fundamental to understanding its behavioural ecology and a prerequisite to planning its management. Few data exist on the spatial ecology of cheetahs Acinonyx jubatus outside protected areas, but such areas are particularly important to their conservation. Cheetahs on Namibian farmlands occupied exceptionally large home ranges, averaging 1651 km² (±1594 km²), with no detectable effect of sex, social grouping or seasonality. Despite such large ranges, cheetahs tended to utilize intensively only a small fraction of that area: 50% of the fixes were located within an average of 13.9±5.3% of the home range. Ranges were not exclusive, overlapping on average by 15.8±17.0%, with male cheetahs showing more intra-sexual range overlap than did females. Coalitions of males appeared to select for a dense, prey-rich habitat, but this preference was not apparent for other social groupings. Conflict with humans is an important contributor to the species' decline, and these large, overlapping cheetah home ranges result in the movements of each individual cheetah encompassing many farms (21 based on the average home-range size). Consequently, many cheetahs may be exposed to a minority of farmers attempting to kill them, and also that many farmers may see the same cheetahs, thereby gaining an exaggerated impression of their abundance. Conservation priorities for cheetahs outside protected areas are the development of techniques for conflict resolution, as well as the maintenance and restoration of suitable habitat and promotion of land-management practices compatible with the continued existence of large carnivores.     

Wintering site fidelity and movement patterns of Western Sandpipers Calidris mauri in the San Francisco Bay estuary

Western Sandpipers Calidris mauri are the most numerous shorebird species in the San Francisco Bay estuary during winter. A sample of 106 Western Sandpipers was captured in mist nets and radio-marked with 1-g transmitters to examine their wintering site fidelity and movements. Differences in distances moved, home range extent and core area size were examined by age, sex, season, site, time of day and tide. All birds remained in the south San Francisco Bay region during winter and exhibited strong site fidelity, with a mean home range of 22.0 km² or only 8% of the study area. First-year birds had larger home ranges (26.6 ± 3.6 km²) than adults (17.2 ± 2.5 km²) in winter, but home range sizes of males and females were not significantly different in any period. Home range sizes were similar between seasons, but core areas were smaller in spring (6.3 ± 1.2 km²) than in early (9.6 ± 4.0 km²) or late (11.6 ± 1.6 km²) winter. Movements and home range size were similar for radio-marked birds located during day and night. The high degree of regional and local site fidelity demonstrated that the mixture of natural mud fiats and artificial salt ponds in southern San Francisco Bay provided sufficient resources for large wintering populations of Western Sandpipers.     

Jaguar spacing, activity and habitat use in a seasonally flooded environment in Brazil

Between July 1980 and February 1984, six jaguars (two males, four females) were fitted with radio-collars and monitored for a cumulative total of 105 months, in the Pantanal region of southwestern Brazil. Mean home range size (minimum convex polygon) for five of them (one male, four females) was 142- 1 km². Mean home range size during the dry season was 54·3 km², whereas in the wet season it was significantly smaller, 12·8 km². Mean home range overlap of the four females was 42%. Use of gallery forest and forest patches exceeded the availability of these habitat types in the animals' home ranges, whereas open forest and grassland were used less than expected on the basis of their availability. Mean distance moved between locations on consecutive days was 2·4 km (0.2-10·4 km). The mean one-day movement of the male jaguar was significantly (P<0·001) larger than that of the females. Mean distance travelled by all animals during one-day intervals in the dry season was significantly greater (P<0·001) than that travelled in other months. Jaguars were more active during daytime than night-time (P<0·001). Overall level of activity for the wet season did not differ from that of the dry season. With their larger body size, jaguars in the Pantanal may require more food than jaguars in other areas of the species' range. This, in addition to differences in prey availability and the annual availability of dry land, appear to influence the difference in home range size between jaguar populations.     

Behavioural ecology of the Greater one-horned rhinoceros (Rhinoceros unicornis)

In the Chitawan Valley of Nepal there were estimated to be between 270 and 310 Greater one-horned or Indian rhinoceroses (Rhinoceros unicornis L.). Population densities reached 4.85 rhinos/km² in the favoured areas of high diversity of early successional vegetation types on the valley floor. The overall population composition was 32.3% adult females, 19.9% adult males, 21.2% sub-adults and 26.6% calves. Females first calved at a mean age of 7.1 years and the median intercalving interval was 2.8 years. Causes of death included poaching, tiger predation on calves and fighting among males. The population was increasing.
Rhinos fed from 183 species of plants belonging to 57 botanical families but grass (50 species) made up between 70 and 89% of their diet according to the season. Considerable seasonal variations in food availability resulted in movements of rhinos between vegetation types. Rhinos' ranges were smallest in the areas of greatest vegetational diversity.
Rhinos rarely formed groups. The most common type consisted of sub-adults–mainly males. Ten auditory displays were distinguished and visual displays, although less striking, included baring the lower incisor tusks. Scents were carried in the dung, the urine and the pedal scent glands. Squirt urination and foot-dragging displays were performed by breeding males only.
There was some degree of range exclusivity among breeding males but no true territoriality. Poor visibility and the relatively unpredictable distribution of resources in time and space have perhaps selected against a territorial mating system. Relationships between ecology and social organization are discussed with reference to other rhino species.
Threats to the continued survival of the Indian rhino include poaching, agricultural encroachment and erosion. In order to spread the risk of a catastrophe, reintroductions of rhinos to other protected areas are proposed.     

Ranging behaviour and foraging habitats of breeding Sparrowhawks Accipiter nisus in a continuous forested area in Norway

The ranging behaviour and foraging habitats of Sparrowhawks Accipiter nisus were studied in a continuous forest area in southern Norway by use of radiotelemetry in 1995 and 1996. The mean size of the home ranges was 9.2 km² for males (sd ± 3.7, n = 6) and 12.3 km² for females (sd ± 6.4, n = 6), but the difference was not significant. Females ranged farther away from nests (mean 1824 m) than did males (mean 1240 m). None of the Sparrowhawks were located outside forest habitats. For the three pairs where both mates were radiotracked in 1996, habitat use did not differ between the sexes. Habitat composition in the home ranges differed from that of the study area. The most important difference was a higher proportion of medium-aged forest and a lower proportion of old forest in home ranges than in the study area. The selection for medium-aged forests was probably a response to high food supply and good hunting opportunities. Mixed regeneration and old forests were used more than clear-fell areas, which were seldom used. Mixed regeneration was also used more than coniferous replanting. The large home ranges in this study compared with those in studies in Great Britain is probably due to lower land productivity and associated lower densities of prey species in the present study. The study indicates that the Sparrowhawk benefits from modern forestry, which has created an increased proportion of medium-aged stands in the forest landscape.     

White rhinoceros range size in the south-western Kruger National Park

White rhinoceros range size was ascertained telemetrically in the south-western Kruger National Park. The mean annual range size of territorial males was 9.86 km² compared to 22.83 km² for adult females. White rhinoceros females' summer wet season range was larger (21.44 km²) than the winter dry season range (11.64 km²). It is argued that abundant field-water during the wet season enables animals to range further from permanent water supplies and to utilize larger foraging areas. White rhinoceros have core areas in their individual ranges that usually are situated along riverbanks in the preferred grazing regions. These core areas also include some favourite resting spots on high-lying areas. White rhinoceros range sizes in the south-western Kruger National Park were similar to those of other reserves with comparable white rhinoceros densities. In the Umfolozi Game Reserve, which has a higher white rhinoceros density than the Kruger National Park, the individual ranges are much smaller.     

The demography of a high-density badger (Meles meles) population in the west of England

Data from the longest running capture-mark-recapture study of Eurasian badgers, in an undisturbed wild population at Woodchester Park in Gloucestershire, were used to investigate population dynamics. Twenty-one social groups of badgers occupying an area of 7.3km² were studied from 1978-1993. The density increased steadily over the study period, reaching the highest published density known anywhere at 25.3 adults per km² in 1993, and the average social group size increased to 8.8 adults (S.E. ± 0.85) in 1993. By 1993, 97% of the population trapped was of known age and overall the population consisted of 27% cubs and 73% adults. In addition, the results supported previous studies in that the population had an equal sex ratio as cubs, but became increasingly female biased with age. There was high juvenile mortality, nearly 50% dying in their first year. Between 58 and 90.2% of adult females did not breed each year.     

Home range of the raccoon dog (Nyctereutes procyonoides) in southern Finland

Home ranges, relationships between individuals and dispersal among raccoon dogs ( Nyctereutes procyonoides ) were studied in southern Finland in 1989-91. The average maximum home range, calculated by the harmonic mean method. was 9·5 km² and the core area (85% utilization) 3·4 km². There were no statistically significant annual. seasonal or sexual differences in the size of the average core area of adults, but the home ranges of juveniles in autumn were larger than those of adults. However. the maximum home ranges of adults were larger in autumn than in summer, especially those of males, which were conspicuously small in summer and large in autumn. The core areas of adjacent pairs did not usually overlap in the pup-rearing season. but in autumn some home ranges shifted and there was much more overlap. The home ranges of the male and female of a pair overlapped almost totally, and a male and a female sharing the same home range also travelled together or close to each other, thus supporting the idea that the raccoon dog is monogamous in Finland. None of the adults left the study area, but 38% of the juveniles were recovered further than 10 km from the marking place during the first autumn.     

Behavioural ecology of the Sloth bear (Melursus ursinus)

The Sloth bear ( Melursus ursinus ), which is endemic to the Indian subcontinent and Sri Lanka, has declined in numbers in many areas in recent years probably as the result of over-killing and habitat alteration. In the 544 km² Royal Chitawan National Park in the Nepal terai, we estimated there were a minimum of 55 bears or a crude density of 0˙1/km². During peak concentrations in the lowlying riverine forest/tall grass habitat in March, the ecological density was 0˙5/km².
Cubs still with their mothers comprised 24 % of the 161 bears classified between December 1972 and November 1975. Females comprised 48% of the adults classified. Average size of 24 litters was 1˙6 (1–2). Seventy-two per cent of the observations were of lone individuals. Three (an adult female with two cubs), was the largest group of bears seen. The only extended social group observed was the female-young unit although newly independent siblings may remain together for a short time. Maternal relations, adult interactions, tree marking, ranging, feeding and anti-predatory behaviour are described.
Examination of 139 droppings showed that these bears fed on at least 17 different fruits (47% occurrence), flowers, grass, honey, and six different insects (52% occurrence). Fruits were an important food from March to June with individual species predominating throughout their fruiting season. Termites, including Odontotermes obesus , were in the diet for most of the year. The Sloth bear was not observed preying on mammals and according to other observers, only rarely feeds on carrion. The ecological basis for selected aspects of Sloth bear biology and behaviour is discussed.     

Home range size and distribution in a wild population of Cape pangolins, Manis temminckii, in north‐west Zimbabwe

The aim of this study was to estimate the size of the home range used by individual Cape pangolins ( Manis temminckii ). The study was conducted in 1991–95 at Sengwa Wildlife Research Institute, Gokwe, Zimbabwe. Radio‐telemetry was used to repeatedly locate study pangolins. Home range area was estimated from the location of the burrows used by each pangolin. It was established that pangolins must be tracked for 85+ days to generate a reliable estimate of home range. The size of home ranges, determined from 1141 tracking days of data for 10 pangolins (3·0–15·8 kg body mass) that were each tracked for at least 85 days, was from 0·17 to 11·07 km². Larger (older) pangolins used more burrows and had larger home ranges than smaller (younger) pangolins. The data indicate that large adult males had larger home ranges than large adult females. Within each sex, the home ranges were adjacent to each other with only slight overlap at the boundaries. There was clear overlap of home ranges between males and females.     

Home range and habitat use by the serotine bat, Eptesicus serotinus, in England

Serotine nursery roosts with less than 20 bats were found to have home ranges of at least 24 to 77 km² and core areas of activity from 13 to 33 km². The size of the range may have increased further if more individuals had been tracked, as three of the four colonies studied had not reached their asymptotes. The total home-range area covered by four serotine colonies was 127.36 km². Excluding non-breeding bats, a density of one bat per 120 ha was estimated. However, actual density was likely to be higher if there were additional non-breeding females and immatures that were not in nursery roosts. Colonial home ranges and core areas overlapped, with individuals from different colonies feeding at the same sites. Individual home ranges ( n = 32) varied from 0.16 to 47.58 km², but these were not used exclusively by one individual. Around the colonial core area and breeding roosts, home ranges were used by all individuals from a single colony. It is only further from the core area that ranges appeared to be used by individuals. The distance from roost to feeding areas varied by up to 7.4 km, but the bat usually commuted along lines of trees and hedges and over pastures. This resulted in greater distances being travelled than if they had flown by a direct route. On average, individuals commuted distances of 8 km each night between feeding areas, with a maximum distance of over 41 km. They visited between 0 and 10 feeding sites each night (mean = 2.89).     

Kill rates and food consumption of leopards in Bardia National Park, Nepal

This is the first study presenting data on kill rates and food consumption among Asian leopardsPanthera pardus Linnaeus, 1758. In Bardia National Park, Nepal, we found leopard kills by searching within areas with clusters of locations from radio collared leopards (2 males and 1 female with 2 cubs aged 4–9 months). We used two tracking schemes, 24-h intensive radio-tracking and daily monitoring, and we defined food consumption as the product of average prey live weight and proportion consumed. The three leopards consumed 89.2 kg of meat from five chitalAxis axis, one domestic dog and two birds during 19 days of 24-h intensive tracking, rendering an average (± SE) daily food intake of 4.7 ± 0.3 kgper capita. Twenty-five prey items (14 chital, one muntjacMuntiacus muntjak, four primates and six birds) were found during 180 days of daily monitoring of the female. All edible biomass was consumed in all kills, except for three chital, and the rate of kill consumption was positively related to the age of her cubs. The average daily food consumption of the female was 4.0 ± 0.3 kg/day, the kill rate (days/kill) including all prey categories was 5.6 ± 0.4 days, and the kill rate of ungulates was 10.6 ±0.7 days. Our food consumption estimates are higher than reported from arid African environments. We suggest that the high food consumption rate in our study is a consequence of a release from time-energy constraints due to high prey abundance.