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.     

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.     

HARBOR PORPOISE (PHOCOENA PHOCOENA) ABUNDANCE IN ALASKA: BRISTOL BAY TO SOUTHEAST ALASKA, 1991-1993

Between 1991 and 1993, Alaska harbor porpoise ( Phocoena phocoena ) abundance was investigated during aerial surveys throughout much of the coastal and offshore waters from Bristol Bay in the eastern Bering Sea to Dixon Entrance in Southeast Alaska. Line-transect methodology was used, and only those observations made during optimal conditions were analyzed. Survey data indicated densities of 4.48 groups/100 km², or approximately 3,531 harbor porpoises (95% C. I. 2,206-5,651) in Bristol Bay and 0.54 groups/100 km², or 136 harbor porpoises (95% C. I. 11-1,645) for Cook Inlet. Efforts off Kodiak Island resulted in densities of 1.85 groups/100 km², or an abundance estimate of 740 (95% C. I. 259-2,115). Surveys off the south side of the Alaska Peninsula found densities of 2.03 groups/100 km² and an abundance estimate of 551 (95% C. I. 423-719). Surveys of offshore waters from Prince William Sound to Dixon Entrance yielded densities of 4.02 groups/100 km² and an abundance estimate of 3,982 (95% C. I. 2,567-6,177). Combining all years and areas yielded an uncorrected density estimate of 3.82 porpoises per 100 km², resulting in an abundance estimate of 8,940 porpoises (CV = 13.8%) with a 95% confidence interval of 6,746-11,848. Using correction factors from other studies to adjust for animals missed by observers, the total number of Alaska harbor porpoises is probably three times this number.     

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.     

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.     

Autumn migration and wintering areas of Peregrine Falcons Falco peregrinus nesting on the Kola Peninsula, northern Russia

Four female Peregrine Falcons Falco peregrinus breeding on the Kola Peninsula, Russia, were fitted with satellite-received transmitters in 1994. Their breeding home ranges averaged 1175 (sd = ±714) km², and overlapped considerably. All left their breeding grounds in September and migrated generally south-west along the Baltic Sea. The mean travel rate for three falcons was 190 km/day. Two Falcons wintered on the coasts of France and in southern Spain, which were, respectively, 2909 and 4262 km from their breeding sites. Data on migration routes suggested that Falcons took a near-direct route to the wintering areas. No prolonged stopovers were apparent. The 90% minimum convex polygon winter range of a bird that migrated to Spain encompassed 213 km² ( n  = 54). The area of the 50% minimum convex polygon was 21.5 km² ( n  = 29). Data from this study agree with others from North America that show that Falcons breeding in a single area do not necessarily follow the same migratory path southward and do not necessarily use the same wintering grounds.     

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.     

Preliminary estimates of the population density of the Sokoke scops owl Otus ireneae Ripley in the East Usambara lowlands, Tanzania

Preliminary population density estimates are presented for a recently discovered population of the Sokoke scops owl Otus ireneae in the lowlands of the East Usambara mountains, Tanzania. Calling birds were mapped at two sites totalling 6·3 km². Approximate densities were 3–4 territories/km² in Kwamgumi Forest Reserve and <1·5 territories/km² in Manga Forest Reserve, a much more heavily logged site. Densities in prime habitat in Arabuko‐Sokoke forest, Kenya, the only other locality for the species, exceed seven territories/km². The total population in the East Usambaras cannot be calculated, but it is probably markedly smaller than in Arabuko‐Sokoke. Suggestions for more precise surveys are made.     

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.     

Ranges of males of the Great Hornbill Buceros bicornis, Brown Hornbill Ptilolaemus tickelli and Wreathed Hornbill Rhyticeros undulatus in Khao Yai National Park, Thailand

Ranges of individual males of three hornbill species were determined by radio telemetry during the breeding and non-breeding seasons in Khao Yai National Park, Thailand. Two Great Hornbills Buceros bicornis and two Brown Hornbills Ptilolaemus tickelli were studied in both 1988 and 1989, and two Wreathed Hornbills Rhyticeros undulatus were studied in 1989, 1990 and 1991.
In the breeding season, the home range of the Great Hornbill was 3.7 km², similar to that of the Brown Hornbill (4.3 km²), while the Wreathed Hornbill occupied the largest home range (10.0 km²). In the non-breeding season, the range size of the Wreathed Hornbill (28.0 km²) was greater than that of the Great Hornbill (14.7 km²). Differences in range sizes of different species may be related to differences in diet and breeding strategy. Ranges overlapped within and between the species, and this has implications for the estimation of the minimum area required for the conservation of hornbills within the Khao Yai National Park.     

Residence and movement patterns of cownose rays Rhinoptera bonasus within a south-west Florida estuary

Between July 2003 and November 2004, 21 cownose rays Rhinoptera bonasus were tagged and tracked within Pine Island Sound estuary, Florida, using passive acoustic telemetry. Residence time of individuals ranged between 1 and 102 days. No relationship was detected between ray activity and tidal stage or time of day. Minimum convex polygons (MCP) and kernel utilization distributions (KUD) were calculated over several time frames to demonstrate the extent of an animal's home range and core areas of use. Total MCPs ranged between 0·81 and 71·78 km² (mean = 22·01 km²), with daily MCPs as large as 25·8 km². Total 95% KUDs ranged between 0·18 and 62·44 km² (mean = 22·63 km²), while total 50% KUDs were smaller, ranging from 0·09 to 9·68 km² (mean = 3·33 km²). Both MCP and KUD areas exhibited a positive relationship with residence time and R. bonasus size. As mobile, pelagic swimmers capable of traversing large distances, these data show that cownose rays travel extensively throughout this estuary, yet may remain within very small areas for extended periods.     

Brazilian Tapir Density in the Pantanal: A Comparison of Systematic Camera-Trapping and Line-Transect Surveys

The density of Brazilian tapirs ( Tapirus terrestris) was studied in the northeastern part of the Pantanal wetlands of Brazil using two simultaneous and independent methods: (1) systematic camera trapping combined with capture–recapture analysis, with camera traps spaced 1 km apart and distributed over 54 km²; and (2) line-transect sampling using an array of 12 linear transects, from 3.8 to 7.2 km long, covering the principal open and forest habitat types across the entire 1063 km² SESC Pantanal Reserve. The two methods yielded conservative density estimates of 0.58 ± 0.11 tapirs/km² (camera trapping) and 0.55 (95% CI 0.30–1.01) tapirs/km² (line transects). The study suggests that certain Pantanal habitats and sites can sustain relatively high population densities of tapirs when these animals are protected from hunting. Further testing of the camera-trapping methodology as applied to tapirs is required, particularly focusing on extending the survey period. As it represents a relatively rapid method for estimating population density, in comparison to line-transect surveys, and as it generates information simultaneously on multiple species that are conservation priorities, we recommend that camera-trapping surveys be applied more widely across a variety of Pantanal habitats and land-use categories in order to confirm the value of the vast 140,000 km² wilderness region for this vulnerable species.     

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).     

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.     

Carrying Capacity and Potential Production of Ungulates for Human Use in a Mexican Tropical Dry Forest

Data are provided on the carrying capacity and potential production for sustainable human use of white-tailed deer ( Odocoileus virginianus ) and collared peccary ( Pecari tajacu ) in a protected tropical dry forest at Chamela on the Pacific coast of Mexico. In this paper, the carrying capacity was defined as the equilibrium density plus the number of animals removed by predators. The equilibrium point was estimated from the density dependent relationship between the finite population growth rate and the current density according to a logistic model. Annual density was estimated using the line transect method. Carrying capacity estimates were 16.5 to 17.2 deer/km² and 9.3–9.5 peccaries/km², representing a combined biomass of 841–874 kg/km². A potential production for human use of 2.1 deer/km² and 4.4 peccaries/km² was estimated employing the model of Robinson and Redford (1991) . The data suggest that, in the protected tropical dry forest of Chamela, the density and biomass of wild ungulates can maintain a similar or greater density and biomass than other Neotropical forests. To obtain an accurate estimation of the maximum sustainable yield ( MSY ), it is necessary to consider predation. From a management point of view, it is important to consider that carrying capacity varies as a function of the rainfall pattern.     

Density and distribution of the ringed seal in the Bothnian Bay

A modified strip census of basking ringed seals in the Bothnian Bay was carried out during the last week of April and the first week of May 1988. Of the total ice covered area, 23174 km², 3236 km² (14%) was covered by the transects. The mean density in the area was 0.101 ringed seals km^-2, with substantial regional and local variation. Highest densities were found in the compact drift ice area. The estimated total population of ringed seals on the ice was 2093 in the Bothnian Bay proper and 248 in the North Quark. The 95% confidence limits of the estimates are ±24%.     

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.     

Estimating species richness at large spatial scales using data from small discrete plots

Estimating species richness in large biomes is a central challenge in ecology and conservation biology. However, accurate census data is often available only from small discrete plots distributed within the biome. Using tree species richness data collected from 48 plots (0.25 ha each) widely distributed through 60 000 km² in the rainforests of the Western Ghats of southern India, we test the application of a proposed method for estimating species richness at large scales from measured species commonalities between pairs of censused plots. We show that the method allows extrapolation of species richness from a scale of 0.25 ha plots to that of the entire biome, or 10⁵ km².     

Movement Patterns and Home Range Of The Bongo (Tragelaphus Eurycerus) In The Rain Forest Of The Dzanga National Park, Central African Republic

Bongos ( Tragelaphus eurycerus Ogilby) were studied for 8 months in the Dzanga National Park, Central African Republic. Tracks were followed and mapped with a compass and a pedometer to study movement patterns and home range. Natural licks were shown to be central points in the home range of the bongos: they visited the licks recurrently to consume soil, but also to forage on grass and herb species, and for social reasons. Forest areas far from licks were used much less than forest areas close to licks. When a lick was visited, distances between two resting sites were longer than in the forest without lick visits, caused by a direct and straight movement from the denser forest areas toward a lick. The study area of about 150 km² was presumably occupied by two groups of bongos. One of them seemed to split temporarily into two subgroups. Groups were not larger than 10–20 individuals. Estimated home ranges were at least 49 km² and 19 km² for the two groups, respectively. Estimated density in the Dzanga National Park was 0.25 bongos per km^2. This study shows the importance of natural licks for the largest social forest antelope, the bongo, and provides information which is important for its future conservation.     

Determinants of avian species richness at different spatial scales

ABSTRACT. Studies of factors influencing avian biodiversity yield very different results depending on the spatial scale at which species richness is calculated. Ecological studies at small spatial scales (plot size 0.0025–0.4 km²) emphasize the importance of habitat diversity, whereas biogeographical studies at large spatial scales (quadrat size 400–50,000 km²) emphasize variables related to available energy such as temperature. In order to bridge the gap between those two approaches the bird atlas data set of Lake Constance was used to study factors determining avian species diversity at the intermediate spatial scales of landscapes (quadrat size 4–36 km²). At these spatial scales bird species richness was influenced by habitat diversity and not by variables related to available energy probably because, at the landscape scale, variation in available energy is small. Changing quadrat size between 4 and 36 km², but keeping the geographical extension of the study constant resulted in profound changes in the degree to which the amount of different habitat types was correlated with species richness. This suggests that high species diversity is achieved by different management regimes depending on the spatial scale at which species richness is calculated. However, generally, avian species diversity seems to be determined by spatial heterogeneity at the corresponding spatial scale. Thus, protecting the diversity of landscapes and ecosystems appears to ensure also high levels of species diversity.