The ranging patterns of elephants in Marsabit protected area,Kenya: the use of satellite‐linked GPS collars

We investigated the ranging patterns of elephants in the Marsabit protected area, north eastern Kenya, to ascertain the range of bachelor and female family herds in different seasons, and to identify corridor and noncorridor areas. Data were acquired for five bachelor and four female family herds equipped with satellite‐linked geographical positioning system collars, and monitored from December 2005 to December 2007. Distinct dry (about 260 km²) and wet seasons (about 910 km²) ranges were observed, with connecting corridors (north‐eastern corridor: about 90 km long, about 2‐7 km wide; southern corridors: about 10‐20 km long, about 2‐3 km wide). The dry season range corresponded with Marsabit evergreen forest, while the wet season range matched with dry deciduous lowland shrubs. The ranging elephants moved at speed of about 0.2‐20 kmh^?1. Bachelor herds moved faster than female family herds. Elephants moved fast during the intermediate and wet seasons than during the dry season. The speed of ranging elephants was over 1 kmh^?1 in the corridor areas and about 0.2 to less than 1 kmh^?1 in the non‐corridor areas. Expansion of settlements towards corridor areas needs to be controlled to avoid future blocking of connectivity between wet and dry season elephant ranges.     

Spatial ecology and habitat use of giraffe (Giraffa camelopardalis) in South Africa

The lack of long-term studies remains a limiting factor in understanding the home range, spatial ecology and movement of giraffes. We equipped eight giraffes with GPS satellite units and VHF capacity, which were built in to the collars for the remote collection of data on their movements and home ranges over two years on Khamab Kalahari Nature Reserve (KKNR) within the Kalahari region of South Africa. Giraffe numbers in KKNR dropped from 135 individuals to 111 in just five years, revealing the lack of knowledge about their required habitat needs, space use and diet. With over 1000 km² available for roaming within the reserve, habitat selection, principle and preferred food species played a significant role in home range size and overlap between individuals. These giraffes used an average annual home range of 206 km² (20 602 ha) as calculated by a 95% minimum convex polygon (MCP) with a standard deviation core home range calculated by a 50% MCP of 10.1 km² to satisfy their annual needs for survival and reproduction in their preferred vegetation. In the wet, hot season (summer: December–February) when food was abundant, giraffes frequented smaller areas (average 177 km²), while in the dry, cool season (winter: June to August) the mean home range size increased to approximately 245 km². Rainfall influenced spatial distribution since it determined vegetation productivity and leaf phenology. The different seasons influenced giraffe movements, while different vegetation types and season influenced their home range size. Season and food availability also influenced home range overlap between different giraffe herds. Home range overlap occurred when giraffes were forced to roam in overlapping areas during the dryer months when the winter deciduous nature of the majority of the tree species resulted in lower food availability. In winter, the overlap was approximately 31% and in autumn approximately 23%. During the wet and warmer months, overlapping was 15% in summer and 19% in spring, respectively. The percentage of time spent in different vegetation type areas was influenced by the abundance of the principal food species of that plant community. It is thus concluded that the movements of giraffes were primarily influenced by a combination of environmental factors such as season, rainfall and vegetation density.     

Seasonal movements of Gyrfalcons Falco rusticolus include extensive periods at sea

Little information exists on the movements of Gyrfalcons Falco rusticolus outside the breeding season, particularly amongst High Arctic populations, with almost all current knowledge based on Low Arctic populations. This study is the first to provide data on summer and winter ranges and migration distances. We highlight a behaviour previously unknown in Gyrfalcons, in which birds winter on sea ice far from land. During 2000–2004, data were collected from 48 Gyrfalcons tagged with satellite transmitters in three parts of Greenland: Thule (northwest), Kangerlussuaq (central‐west) and Scoresbysund (central‐east). Breeding home‐range size for seven adult females varied from 140 to 1197 km² and was 489 and 503 km² for two adult males. Complete outward migrations from breeding to wintering areas were recorded for three individuals: an adult male which travelled 3137 km over a 38‐day period (83 km/day) from northern Ellesmere Island to southern Greenland, an adult female which travelled 4234 km from Thule to southern Greenland (via eastern Canada) over an 83‐day period (51 km/day), and an adult female which travelled 391 km from Kangerlussuaq to southern Greenland over a 13‐day period (30 km/day). Significant differences were found in winter home‐range size between Falcons tagged on the west coast (383–6657 km²) and east coast (26 810–63 647 km²). Several Falcons had no obvious winter home‐ranges and travelled continually during the non‐breeding period, at times spending up to 40 consecutive days at sea, presumably resting on icebergs and feeding on seabirds. During the winter, one juvenile female travelled over 4548 km over an approximately 200‐day period, spending over half that time over the ocean between Greenland and Iceland. These are some of the largest winter home‐ranges ever documented in raptors and provide the first documentation of the long‐term use of pelagic habitats by any falcon. In general, return migrations were faster than outward ones. This study highlights the importance of sea ice and fjord regions in southwest Greenland as winter habitat for Gyrfalcons, and provides the first detailed insights into the complex and highly variable movement patterns of the species.     

Population status and habitat preference of Soemmerring’s gazelle in Alledeghi Wildlife Reserve,Eastern Ethiopia

This study was undertaken to determine the current population size, structure and habitat preference of Soemmerring's gazelle [Nanger soemmerringii (Cretzschmar 1828)] in the Alledeghi Wildlife Reserve, NE Ethiopia. Animals were counted, both during dry and wet seasons, along 12 line transects each in three habitat types (grassland, tree‐scattered grassland and bushland) in 2015/16. Habitat type had nonsignificant effect on mean population density of Soemmerring's gazelle, but wet season mean density was significantly higher than dry season mean density. Estimated weighted mean (±95% CI) population density of the species in the reserve was 1.90 (±0.17) and 5.99 (±0.370) individuals/km² during the dry and wet seasons, respectively. Total population size of the species in the Alledeghi Wildlife Reserve was estimated at 826 ± 77 and 2,562 ± 158 individuals during the dry and wet seasons, respectively. Over half of the total population of Soemmerring's gazelle was represented by adult females during both seasons. Seasonal habitat preference of Soemmerring's gazelle was statistically significant, with greater preference for grassland habitat during wet season and for bushland habitat during dry season. In conclusion, this study has provided valuable data that will be used as a baseline for future population monitoring.     

Changes in lion (Panthera leo) home range size in Waza National Park,Cameroon

The spatial ecology of Africa lions (Panthera leo) was studied from 2007 to 2009 in Waza National Park, Cameroon, by equipping individual lions with GPS/VHF radio-collars. Mean home range estimates using 100% minimum convex polygons (MCP) and 95% kernel-density estimation (KDE) were respectively 1015 km² and 641 km². The lions spent a considerable amount of time out of the park during the study period (21%), resulting in significantly larger wet season home ranges than in the hot dry season when they were largely within the park. Time spent outside of the park coincided with increased livestock predation, especially by males. The seasonal variation observed in home range appeared to be mainly due to prey dispersal, flooding and migrating livestock. Mean home range size was observed to have increased by 58.6% within the last decade. This observed increase in home range could possibly be attributed to recent declines in wild prey abundance and also, may be indicative of a trend of general degradation of the park due to intense human pressure. The change observed in lions’ ranging behaviour was remarkable, with lions crossing the highway parallel to the park to the Cameroon-Nigerian borders. Measures to restore the integrity of the park are urgently needed, which could include the construction of a partial fence along the western boundary of the park to prevent lions moving across the parallel highway.     

Habitat suitability assessment of Sichuan sika deer in Tiebu Nature Reserve during periods of green and dry grass

Habitat suitability assessment is an essential and dynamic research method for determining and evaluating the environmental pressures faced by wildlife. From March to November 2011, we investigated the quality of habitat available to Sichuan sika deer (Cervus nippon sichuanicus) in Tiebu Nature Reserve, Ruoergai County, Sichuan Province, China. A habitat evaluation model established by the fuzzy assignment quadrature method was used to assess habitat suitability for Sichuan sika deer within the reserve by using the GIS spatial analysis function. The results showed that the area of actual available habitat was 220.8 km² during the wet season and 213.2 km² during the dry season, accounting for 80.8% and 78.02% of the total nature reserve area, respectively. The area of suitable habitat for Sichuan sika deer was much lower, 128.01 km² during the wet season and 109.17 km² during the dry season, accounting for 46.84% and 39.95% of the total nature reserve area respectively. The difference between available and suitable habitat is likely due to potentially good habitat having been lost as a result of human disturbance. Lost habitat makes up 4.55% of the total area while grass is green and 5.52% while grass is dry. Human disturbance levels in the form of roads and residential areas were constant throughout the year, but grazing by domestic animals had a higher impact during the dry season. Habitat suitability during this time, already reduced by the withering of the grass, was thus further reduced by the grazing of livestock.     

Standardising Home Range Studies for Improved Management of the Critically Endangered Black Rhinoceros

Comparisons of recent estimations of home range sizes for the critically endangered black rhinoceros in Hluhluwe-iMfolozi Park (HiP), South Africa, with historical estimates led reports of a substantial (54%) increase, attributed to over-stocking and habitat deterioration that has far-reaching implications for rhino conservation. Other reports, however, suggest the increase is more likely an artefact caused by applying various home range estimators to non-standardised datasets. We collected 1939 locations of 25 black rhino over six years (2004–2009) to estimate annual home ranges and evaluate the hypothesis that they have increased in size. A minimum of 30 and 25 locations were required for accurate 95% MCP estimation of home range of adult rhinos, during the dry and wet seasons respectively. Forty and 55 locations were required for adult female and male annual MCP home ranges, respectively, and 30 locations were necessary for estimating 90% bivariate kernel home ranges accurately. Average annual 95% bivariate kernel home ranges were 20.4 ± 1.2 km², 53 ±1.9% larger than 95% MCP ranges (9.8 km² ± 0.9). When home range techniques used during the late-1960s in HiP were applied to our dataset, estimates were similar, indicating that ranges have not changed substantially in 50 years. Inaccurate, non-standardised, home range estimates and their comparison have the potential to mislead black rhino population management. We recommend that more care be taken to collect adequate numbers of rhino locations within standardized time periods (i.e., season or year) and that the comparison of home ranges estimated using dissimilar procedures be avoided. Home range studies of black rhino have been data deficient and procedurally inconsistent. Standardisation of methods is required.     

Seasonal habitat use by Elephants (Loxodonta africana) in the Mole National Park of Ghana

To avoid unnecessary waste of limited resources and to help prioritize areas for conservation efforts, this study aimed to provide information on habitat use by elephants between the wet and dry seasons in the Mole National Park (MNP) of Ghana. We compiled coordinates of 516 locations of elephants’ encounters, 256 for dry season and 260 for wet season. Using nine predictor variables, we modeled the probability of elephant's distribution in MNP. We threshold the models to “suitable” and “nonsuitable” regions of habitat use using the equal training sensitivity and specificity values of 0.177 and 0.181 for the dry and wet seasons, respectively. Accuracy assessment of our models revealed a sensitivity score of 0.909 and 0.974, and a specificity of 0.579 and 0.753 for the dry and wet seasons, respectively. A TSS of 0.488 was also recorded for the dry season and 0.727 for the wet season indicating a good model agreement. Our model predicts habitat use to be confined to the southern portion of MNP due to elevation difference and a relatively steep slope that separates the northern regions of the park from the south. Regions of habitat use for the wet season were 856 km² and reduced significantly to 547.68 km² in the dry season. We observed significant overlap (327.24 km²) in habitat use regions between the wet and dry seasons (Schoener's D = 0.922 and Hellinger's‐based I = 0.991). DEM, proximity to waterholes, and saltlicks were identified as the key variables that contributed to the prediction. We recommend construction of temporal camps in regions of habitat use that are far from the headquarters area for effective management of elephants. Also, an increase in water point's density around the headquarters areas and selected dry areas of the park will further decrease elephant's range and hence a relatively less resource use in monitoring and patrols.     

Insights into post-fledging dispersal of Bearded Vultures Gypaetus barbatus in southern Africa from GPS satellite telemetry

Capsule: Fledglings progressively increase their home range size and ranging behaviour as they age.

Aims: To examine the home range size and ranging behaviour of Bearded Vulture fledglings during the post-fledging dependence period and determine the onset of natal dispersal.

Methods: Post-fledging movements of three individuals were investigated in southern Africa using global positioning system (GPS) satellite telemetry which enabled home range sizes and distances travelled from the nest to be calculated.

Results: Fledglings increased their home range size from an average of 0.4–10 999?km² (100% Minimum Convex Polygons) and 9.13–11 466?km² (fixed 95% kernels) within the first six months post fledging. They also increased home range use as they aged with maximum daily distances travelled from the nest occurring between 98 and 136 days post fledging (when fledglings were aged between 222 and 262 days), after which time they dispersed from their natal area. Distances between fixes were highest during the dispersal period.

Conclusion: GPS satellite telemetry allows us to accurately demonstrate how fledglings progressively increase and use their home ranges as they age and undertake pre-dispersive exploratory flights. Results confirm the notion that juveniles disperse at the onset of the following breeding season and suggest that dispersal occurs earlier in the southern hemisphere.     

Home on the range: spatial ecology of loggerhead turtles in Atlantic waters of the USA

Aim Although satellite tracking has yielded much information regarding the migrations and habitat use of threatened marine species, relatively little has been published about the environmental niche for loggerhead sea turtles Caretta caretta in north‐west Atlantic waters. Location North Carolina, South Carolina and Georgia, USA. Methods We tracked 68 adult female turtles between 1998 and 2008, one of the largest sample sizes to date, for 372.2 ± 210.4 days (mean ± SD). Results We identified two strategies: (1) ‘seasonal’ migrations between summer and winter coastal areas (n = 47), although some turtles made oceanic excursions (n = 4) and (2) occupation of more southerly ‘year‐round’ ranges (n = 18). Seasonal turtles occupied summer home ranges of 645.1 km² (median, n = 42; using α‐hulls) predominantly north of 35 ° latitude and winter home ranges of 339.0 km² (n = 24) in a relatively small area on the narrow shelf off North Carolina. We tracked some of these turtles through successive summer (n = 8) and winter (n = 3) seasons, showing inter‐annual home range repeatability to within 14.5 km of summer areas and 10.3 km of winter areas. For year‐round turtles, home ranges were 1889.9 km². Turtles should be tracked for at least 80 days to reliably estimate the home range size in seasonal habitats. The equivalent minimum duration for ‘year‐round’ turtles is more complex to derive. We define an environmental envelope of the distribution of North American loggerhead turtles: warm waters (between 18.2 and 29.2 °C) on the coastal shelf (in depths of 3.0–89.0 m). Main conclusions Our findings show that adult female loggerhead turtles show predictable, repeatable home range behaviour and do not generally leave waters of the USA, nor the continental shelf (< 200m depth). These data offer insights for future marine management, particularly if they were combined with those from the other management units in the USA.     

BIODIVERSITY RESEARCH: Fidelity to foraging sites,consistency of migration routes and habitat modulation of home range by sea turtles

Aim Resources can shape patterns of habitat utilization. Recently a broad foraging dichotomy between oceanic and coastal sites has been revealed for loggerhead sea turtles (Caretta caretta). Since oceanic and coastal foraging sites differ in prey availability, we might expect a gross difference in home‐range size across these habitats. We tested this hypothesis by equipping nine adult male loggerhead sea turtles with GPS tracking devices. Location National Marine Park of Zakynthos (NMPZ) Greece, central and eastern Mediterranean (Adriatic, Ionian and Aegean seas). Methods In 2007, 2008 and 2009, Fastloc GPS‐Argos transmitters were attached to nine male loggerheads. In addition, a Sirtrack PTT unit was attached to one male in 2007. Four of the turtles were tracked on successive years. We filtered the GPS data to ensure comparable data volumes. Route consistency between breeding and foraging sites of the four re‐tracked turtles was conducted. Foraging site home range areas and within site movement patterns were investigated by the fixed kernel density method. Results Foraging home range size ranged between circa 10 km² at neritic habitats (coastal and open‐sea on the continental shelf) to circa 1000 km² at oceanic sites (using 90% kernel estimates), the latter most probably reflecting sparsely distributed oceanic prey. Across different years individuals did not follow exactly the same migration routes, but did show fidelity to their previous foraging sites, whether oceanic or neritic, with accurate homing in the final stages of migration. Main conclusions The broad distribution and diverse life‐history strategies of this population could complicate the identification of priority marine protected areas beyond the core breeding site.     

四川羚牛的家域与忠诚度

野生动物倾向回到或留在一个特定范围或者与原有区域完全重叠的行为被称为栖息地忠诚。利用GPS无线电颈圈对5只四川羚牛的家域及家域的季节和年度忠诚度进行了研究和分析(2006—2009年)。结果显示:四川羚牛年均家域面积为(MCP/FKE)(15.01±2.92)km2/(9.02±1.85)km2,但个体间及年际波动较大;季节间家域面积差异显著,个体家域的季节变化体现出较一致的变化模式,最大季节家域主要集中于春季和夏季。年际间季节家域忠诚度最高的是秋季和夏季,冬季家域年际忠诚度最低,春季家域忠诚度也相对较低。单因素方差分析显示季节间质心距离总体差异不显著,与家域重叠算法获得的忠诚度结论基本一致。     

Historical range and movements of the Elephants in Babile Elephant Sanctuary,Ethiopia

A study on historical range and movement patterns of the African savannah elephants (Loxodonta africana africana) in Ethiopia was made from December 2004 to November 2008. Babile Elephant Sanctuary is one of the strongholds of elephants in the country, where it now supports approximately 27% of the elephant population in Ethiopia. Elephant movement routes and ranges were identified based on interviews of local people and by tracking the animals in the field. Elephants of the Sanctuary were categorized into two distinctive groups or clans based on their movement patterns and their associations to each other. Three major valleys, namely Gobele, Erer and Dakata, were crossed by elephants. Elephants in the population had an estimated annual range of 3014 km². Of this, 85.7% (2583 km²) was inside the Sanctuary and 14.3% (430 km²) outside but adjacent to the Sanctuary. Elephant use outside of the Sanctuary included three different areas: Upper Erer Valley (8 km²), Upper Gobele Valley (48 km²) and west of Gobele Valley (374 km²). The extent of range varied seasonally. During the wet season, elephant range was restricted to Erer Valley and its tributaries (1266 km² and a density of approximately 0.25 animal km^?2), or 42% smaller than the dry season range (1417 km², 0.23 elephant km^?2). Range use was smallest (332 km²) in October to November and from April to May. During the dry season, elephants were found in two distinctive groups, one using Gobele Valley and the other Erer Valley.     

Changes in home range size of African lions in relation to pride size and prey biomass in a semi‐arid savanna

Within‐population studies are needed to investigate the extent of, and the factors underlying, intraspecific variation in home range size. We used data from 12 female and 8 male adult lions instrumented with GPS radio‐collars to describe the ranging behaviour of lions in a population from a dystrophic semi‐arid savanna, Hwange National Park, Zimbabwe. We measured prey availability at the home range scale in 2003, 2004, and 2005. For females, home range size increased as pride biomass increased, which is strongly suggestive of expansionism. Once controlled for pride biomass, home range size decreased as prey biomass increased. Pride ranges responded to changes in food abundance on an annual timescale rather than on a seasonal timescale. Female home range size was influenced by the abundance of kudu in the early dry season, whereas it was influenced by buffalo and young elephant abundance in the late dry season. This study shows that female home range size is mainly driven by the size of the pride, but also by prey abundance. Furthermore, female seasonal home range size may be determined, not only by prey abundance, but also by prey dispersion in the landscape. Home range size of males was driven by both prey biomass and the density of female prides.     

Seasonal variation in grey crowned crane (Balearica regulorum) abundance in the Ngorongoro Crater,Tanzania

There are few quantitative estimates of numbers of Africa's endangered grey crowned cranes (Balearica regulorum), yet conservation of this species will depend on such estimates. We used line-transect distance sampling on multiple 2-km segments of an existing road network to estimate the abundance of grey crowned cranes in a portion of the Ngorongoro Crater, Tanzania, during the wet (April) and dry (August) seasons of 2016. We analysed data from 106 transects on which we observed 174 groups of 1–61 cranes (median and mode = 2). Abundance and density estimates on the areas surveyed were best modelled without group size as a covariate and indicated that mean crane densities were significantly lower in the wet season (2.4/km²) than in the dry season (20.2 cranes/km²). Even based on survey areas of different size, minimum estimated numbers of cranes in the Crater (wet season: 108–133; dry season: 362–401) likely reflect the concentration of cranes in the nonbreeding (dry) season in the perennial wetlands of the Crater and reinforce the notion of the Crater being a key seasonal habitat for crane populations in northern Tanzania, as previously suggested in the literature.     

Estimating brocket deer (<Emphasis Type="Italic">Mazama gouazoubira</Emphasis> and <Emphasis Type="Italic">M. americana</Emphasis>) abundance by dung pellet counts and other indices in seasonal Chiquitano forest habitats of Santa Cruz,Bolivia

We assessed dung and track counts for indexing brocket deer abundance in seasonal habitats on a ranch where hunting is not practiced in the Bolivian lowlands. Surveys were replicated along four 10-km trails (totaling 180 km in the wet season and 90 km in the dry season) through four semideciduous forest habitats. Dung pellets and tracks were identified as belonging to Mazama gouazoubira or M. americana by size and shape. Pellet groups lasted more than 1 month during the dry season, but decayed within 1–2 weeks in the wet season. Mean density estimates based on dung counts varied widely between seasons for gray brockets (from 6.77±4.0 to 30.57±23.5 ind/km²; mean±SD) but not for reds (from 3.52±4.6 to 6.98±7.2 ind/km²). These values were probably too high due to underestimation of daily deposition rate, and were reduced during the wet season because of dung decay. We found consistently more dung in the dry season and more tracks in the wet season. Sightings of red brockets were too few for line-transect analysis (n=6), but those of gray brockets (n=42) produced an overall estimate of 5.6 ind/km² (95% CI=3.5–9.0 ind/km²). Different estimates indicated that gray brockets were more abundant than reds in all situations, except perhaps in the riverine forest. Environmental factors affected these indices of abundance differently, and while we recommend the use of dung counts in dry-season scenarios, we think that index reliability should be assessed locally before conducting population comparisons.     

Potential of a no‐take marine reserve to protect home ranges of anadromous brown trout (Salmo trutta)

The extent to which no‐take marine reserves can benefit anadromous species requires examination. Here, we used acoustic telemetry to investigate the spatial behavior of anadromous brown trout (sea trout, Salmo trutta) in relation to a small marine reserve (~1.5 km²) located inside a fjord on the Norwegian Skagerrak coast. On average, sea trout spent 42.3 % (±5.0% SE) of their time in the fjord within the reserve, a proportion similar to the area of the reserve relative to that of the fjord. On average, sea trout tagged inside the reserve received the most protection, although the level of protection decreased marginally with increasing home range size. Furthermore, individuals tagged outside the reserve received more protection with increasing home range size, potentially opposing selection toward smaller home range sizes inflicted on fish residing within reserves, or through selective fishing methods like angling. Monthly sea trout home ranges in the marine environment were on average smaller than the reserve, with a mean of 0.430 (±0.0265 SE) km². Hence, the reserve is large enough to protect the full home range of some individuals residing in the reserve. Synthesis and applications: In general, the reserve protects sea trout to a varying degree depending on their individual behavior. These findings highlight evolutionary implications of spatial protection and can guide managers in the design of marine reserves and networks that preserve variation in target species' home range size and movement behavior.     

Population structure and spatial ecology of Kordofan giraffe in Garamba National Park,Democratic Republic of Congo

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Seasonal home range use by Japanese monkeys in the snowy Shiga heights

Between December 1974 and November 1975 (157 days), it was found that seasonal home range changes in the Shiga C troop were closely related to food changes, vegetation, and the existence of neighbouring troops. The detailed points clarified may be summarized as follows: (1) The seasonal home range sizes from winter to autumn were 1.23 km², 1.46 km², 1.69 km², and 1.21 km², respectively, and the annual size was 3.66 km²; (2) The food changed from bark and buds of trees in winter to young leaves and stems of grasses and trees in spring and summer, and fruits in autumn; (3) Each home range clearly changed according to the phenology of the plants used as food at each season; (4) The food abundance for the monkeys was extremely poor in winter, relatively poor in summer, plentiful in spring, and the best in autumn; and (5) The Shiga C troop and the neighbouring Shiga B₂ troop overlap in their home ranges in spring and autumn, but are separated during winter and summer.     

Do fences constrain predator movements on an evolutionary scale? Home range, food intake and movement patterns of large predators reintroduced to Addo Elephant National Park, South Africa

Fencing conservation areas is ubiquitous in South Africa, however, the impact of these on predator ecology has not been tested. We used relationships between prey abundance and predator space use to create equations to predict the home range size of lions Panthera leo and leopards Panthera pardus. We then successfully tested these predictions using published data (Phinda, Makalali) and home range estimates from radio collared individuals reintroduced to Addo Elephant National Park. Spotted hyaena Crocuta crocuta ranges also seem food dependent. Lion home ranges in Addo (114 ± 5 km²) required 180 fixes to be accurately estimated, spotted hyaena ranges (91 ± 10 km²) required 200 fixes, and the solitary leopard had 295 fixes for a range of 38 km². There were no sexual differences in home range sizes of lions or hyaenas. The daily food intake rate of lions, measured during continuous follows, was 9.8 kg per female equivalent unit. Dominant male lions (14.3 km for 8.3 kg) traveled furthest but obtained the least amount of food per day compared to subordinate males (8.9 km for 16.0 kg) and females (5.8 km for 17.9 kg). Subordinate males traveled the fastest and during the day, to avoid competition and harassment from the dominant males. From an evolutionary viewpoint, the use of fences for conservation has not affected the natural behaviour of the predators as they still conform to predictions derived from unfenced reserves; that is, prey abundance is the key factor in determining space use of large predators.