Linear roadside remnants: Their influence on den‐use,home range and mating system in bobucks (Trichosurus cunninghami)

Abstract Forest clearance results in a marked change in the dispersion of resources such as food and shelter: from a relatively continuous distribution, to patches and strips of remnant habitat set in a more or less inhospitable matrix. Such changes in the patterns of resource dispersion have the potential to strongly influence the dynamics of social and mating systems of resident animal populations. We studied the den‐use patterns, home range characteristics and mating system of a population of bobucks, Trichosurus cunninghami (Marsupialia: Phalangeridae), permanently resident in linear roadside strips of vegetation in north‐eastern Victoria, Australia in order to gain a greater understanding of the impacts of occupying linear roadside habitats on the behavioural ecology of arboreal marsupials. We radio‐tracked 11 adult females and six adult males and collected 2126 diurnal fixes (mean 125/individual) and 1044 nocturnal fixes (mean 61/individual). Males used significantly more den‐trees (mean 16.5 ± 1.5 den‐trees/individual) than females (mean 7.4 ± 0.6 den‐trees/individual) and had home ranges more than twice the size of those of females (male mean 5.1 ± 0.8 ha, female mean 2.1 ± 0.3 ha). On average, each male's home range overlapped with those of three females; there was little intrasexual home range overlap in either sex. Genetic parentage analysis of all young sampled during the study (n = 22) established that only males that overlapped in home range with females had sired those females' young. All but one male in the study sired multiple young in each of the years they were recorded breeding. These behavioural and genetic data indicate that the roadside population was polygynous, in contrast to the socially monogamous bobuck population we studied in a neighbouring forest patch. These differences in behaviour may reflect patterns of resource distribution in the two habitats.     

两种核域估算方法在野生藏狐家域研究中的比较

核域是野生动物重点利用、含有更多居所、隐蔽场所及依赖性食物资源的区域。关于核域的确定和划分一直存在争议,且很难找到客观的并能准确展示动物生物学信息的数理统计方法。2006 年4 月,2006 年9 ～10月和2007 年1 ～4 月,我们共记录青海省都兰县沟里乡3 只藏狐的199 个活动位点,通过固定核空间(Fixed kernel)和调和平均值(Harmonic mean)模型,结合独立区域法的计算原理,估算藏狐的核域,并对两种估算方法进行比较分析,以确定更理想的核域数学模型。研究结果表明:(1)两种估算方法中核域面积均受到家域总面积的影响,固定核空间法的核域面积受家域总面积影响较大,而且变量系数不稳定; (2) 随着样本量的增加,固定核空间法估算的核域面积逐渐减小,而调和平均值法则增大,前者从数理统计上更好地描述了藏狐对家域资源的利用分布,后者更符合客观实际;(3)调和平均值法在划定家域边界时容易包括不属于家域范围的区域,而在估算核域时可以在一定程度上克服该缺陷;(4)调和平均值法能够真实地反应动物的活动中心,估算的核域中包含有更多的活动位点。因此,尽管在估算藏狐核域时固定核空间法有稳定的计算结果等优点,调和平均值法为更理想的核域估算模型。     

Information‐theoretic model selection affects home‐range estimation and habitat preference inference: a case study of male Reeves’s Pheasants Syrmaticus reevesii

Reeves’s Pheasant Syrmaticus reevesii is a vulnerable forest bird inhabiting broadleaved habitats dominated by oaks Quercus spp. in central China. Identifying home‐ranges and habitat associations is important for understanding the biology of this species and developing effective management and conservation plans. We used information‐theoretic criteria to evaluate the relative performance of four parametric (exponential power, one‐mode bivariate normal, two‐mode bivariate normal and two‐mode bivariate circle) and two non‐parametric models (adaptive and fixed kernel) for estimating home‐ranges and habitat associations of Reeves’s Pheasants. For parametric models, Akaike’s information criterion (AIC_c) and the likelihood cross‐validation criterion (CVC) were relatively consistent in ranking the bivariate exponential power model the least acceptable, whereas the two‐mode bivariate models performed better. The CVC suggested that kernel models, particularly the adaptive kernel, performed best among all six models evaluated. The average core area and 95% contour area based on the model with greatest support were 6.1 and 54.9 ha, respectively, and were larger than those estimated from other models. The discrepancy in estimates between models with highest and the lowest support decreased as the contour size increased; however, home‐range shapes differed between models. Minimum convex polygons that removed 5% of extreme data points (MCP95) were roughly half the size of home‐ranges based on kernel models. Estimates of home‐range and model evaluation were not affected by sample size (> 50 observations for each bird). Inference about habitat preference based on composition analysis and home‐range overlap varied between models. That with strongest support suggested that Reeves’s Pheasants selected mature fir and mixed forest, avoided farmland, and had mean among‐individual home‐range overlaps of 20%. We recommend non‐parametric methods, particularly the adaptive kernel method, for estimating home‐ranges and core areas for species with complex multi‐polar habitat preferences in heterogeneous environments with large habitat patches. However, we caution against the traditional convenience of using a single model to estimate home‐ranges and recommend exploration of multiple models for describing and understanding the ecological processes underlying space use and habitat associations.     

Effects of spatial heterogeneity on butterfly species richness in Rocky Mountain National Park, CO, USA

We investigated butterfly responses to plot-level characteristics (plant species richness, vegetation height, and range in NDVI [normalized difference vegetation index]) and spatial heterogeneity in topography and landscape patterns (composition and configuration) at multiple spatial scales. Stratified random sampling was used to collect data on butterfly species richness from seventy-six 20 × 50 m plots. The plant species richness and average vegetation height data were collected from 76 modified-Whittaker plots overlaid on 76 butterfly plots. Spatial heterogeneity around sample plots was quantified by measuring topographic variables and landscape metrics at eight spatial extents (radii of 300, 600 to 2,400 m). The number of butterfly species recorded was strongly positively correlated with plant species richness, proportion of shrubland and mean patch size of shrubland. Patterns in butterfly species richness were negatively correlated with other variables including mean patch size, average vegetation height, elevation, and range in NDVI. The best predictive model selected using Akaike’s Information Criterion corrected for small sample size (AIC_c), explained 62% of the variation in butterfly species richness at the 2,100 m spatial extent. Average vegetation height and mean patch size were among the best predictors of butterfly species richness. The models that included plot-level information and topographic variables explained relatively less variation in butterfly species richness, and were improved significantly after including landscape metrics. Our results suggest that spatial heterogeneity greatly influences patterns in butterfly species richness, and that it should be explicitly considered in conservation and management actions.     

Home range size, habitat utilisation and movement patterns of suburban and farm cats Felis catus

The movements of 10 house cats (4 desexed females, 5 desexed males and 1 intact male) living on the edge of a suburb adjoining grassland and forest/woodland habitat, and a neighbouring colony of seven farm cats, were examined using radio-telemetry over nine months Nocturnal home range areas of the suburban cats varied between 0 02 and 27 93 ha (mean 7 89 ha), and were larger than diurnal home range areas (range 0 02 to 17 19 ha – mean 2 73 ha) Nocturnal home range areas of cats from the farm cat colony varied between 1 38 and 4 46 ha (mean 2 54 ha), and were also larger than diurnal home range areas (range 0 77 to 3 70 ha – mean 1 70 ha) Home ranges of cats in the farm cat colony overlapped extensively, as did those of cats living at the same suburban residence There was no overlap of home ranges of female cats from different residences, and little overlap between males and females from different residences Four of the suburban house cats moved between 390 m and 900 m into habitat adjoining the suburb Polygons describing the home ranges of these animals were strongly spatially biased away from the suburban environment, though the cats spent the majority of their time within the bounds of the suburb Movements further than 100–200 m beyond the suburb edge were always made at night There is evidence that home range sizes and spatial movement patterns of house cats are largely determined by a) the density and spatial distribution of cats utilising separate food resources, b) the personality and social dominance of individual cats, c) the location of favoured hunting and resting/sunning sites, and, d) barriers such as busy roads     

Combining data from 43 standardized surveys to estimate densities of female American black bears by spatially explicit capture–recapture

Spatially explicit capture–recapture (SECR) models are gaining popularity for estimating densities of mammalian carnivores. They use spatially explicit encounter histories of individual animals to estimate a detection probability function described by two parameters: magnitude (g ₀), and spatial scale (σ). Carnivores exhibit heterogeneous detection probabilities and home range sizes, and exist at low densities, so g ₀ and σ likely vary, but field surveys often yield inadequate data to detect and model the variation. We sampled American black bears (Ursus americanus) on 43 study areas in ON, Canada, 2006–2009. We detected 713 animals 1810 times; however, study area-specific samples were sometimes small (6–34 individuals detected 13–93 times). We compared AIC _c values from SECR models fit to the complete data set to evaluate support for various forms of variation in g ₀ and σ, and to identify a parsimonious model for aggregating data among study areas to estimate detection parameters more precisely. Models that aggregated data within broad habitat classes and years were supported over those with study area-specific g ₀ and σ (ΔAIC _c  ≥ 30), and precision was enhanced. Several other forms of variation in g ₀ and σ, including individual heterogeneity, were also supported and affected density estimates. If study design cannot eliminate detection heterogeneity, it should ensure that samples are sufficient to detect and model it. Where this is not feasible, combing sparse data across multiple surveys could allow for improved inference.     

Home ranges and movement patterns in a vulnerable polecat<Emphasis Type="Italic">Mustela putorius</Emphasis> population

Home range characteristics and movement patterns of four female and six male polecatsMustela putorius Linnaeus, 1758 were studied in Luxembourg using radiotelemetry. Home range size of polecats ranged from 42 to 428 ha with an average of 181 ha. The mean (± SE) home range size of males of (246±45 ha) was significantly larger than that of females (84±17 ha). Polecats concentrated 50% of their space use in only 15% of their home range possibly indicating a patchy environment. Comparing our data with other studies in Europe, polecats seem to occupy approximately the same home range size (except in Switzerland) regardless of population density. Average distance traveled per night by males was 3.6 times greater than that of females. Also, seasonal variation in movements was observed in males but not in females.     

An allometric model of home range formation explains the structuring of animal communities exploiting heterogeneous resources

Understanding and predicting the composition and spatial structure of communities is a central challenge in ecology. An important structural property of animal communities is the distribution of individual home ranges. Home range formation is controlled by resource heterogeneity, the physiology and behaviour of individual animals, and their intra‐ and interspecific interactions. However, a quantitative mechanistic understanding of how home range formation influences community composition is still lacking. To explore the link between home range formation and community composition in heterogeneous landscapes we combine allometric relationships for physiological properties with an algorithm that selects optimal home ranges given locomotion costs, resource depletion and competition in a spatially‐explicit individual‐based modelling framework. From a spatial distribution of resources and an input distribution of animal body mass, our model predicts the size and location of individual home ranges as well as the individual size distribution (ISD) in an animal community. For a broad range of body mass input distributions, including empirical body mass distributions of North American and Australian mammals, our model predictions agree with independent data on the body mass scaling of home range size and individual abundance in terrestrial mammals. Model predictions are also robust against variation in habitat productivity and landscape heterogeneity. The combination of allometric relationships for locomotion costs and resource needs with resource competition in an optimal foraging framework enables us to scale from individual properties to the structure of animal communities in heterogeneous landscapes. The proposed spatially‐explicit modelling concept not only allows for detailed investigation of landscape effects on animal communities, but also provides novel insights into the mechanisms by which resource competition in space shapes animal communities.     

Home range,core areas and movement in the ‘critically endangered’ kipunji (Rungwecebus kipunji) in southwest Tanzania

Understanding how threatened forest primates use a heterogeneous landscape is essential to ensuring their survival. Kipunji (Rungwecebus kipunji) are ‘critically endangered’, arboreal monkeys restricted to two sites in Tanzania. Over 90% of the population lives in the degraded Rungwe‐Kitulo forests of the Southern Highlands. In this study, we present the first comprehensive investigation into daily path length and home range size of kipunji, based on data from four groups followed simultaneously over 70 consecutive days on Mt. Rungwe. The mean daily distance travelled was 1293 m (SE 150.82), and daily distance was not significantly correlated to group size. Using fixed kernel density estimation, an area enclosing 90% of the home range calculated using the ‘reference’ method as a smoothing parameter, measured a mean of 306.18 ha (SE 67), and the core area (50% use) was 86.55 ha (SE 18.73). Using the ‘least‐squares cross validation’ method, the mean home range and core area were 205.45 ha (SE 57.02) and 55.45 ha (SE 14.23) respectively. Home range overlap was extensive, although contact between groups was rare, with >97.30% of all observations within 20 min separated by >250 m. The data strongly suggest that kipunji are not territorial.     

Spatial relationship among individuals of the Japanese lacertidTakydromus tachydromoides (Sauria,Lacertidae)

The home range ofTakydromus tachydromoides was studied in a grassland area from April 1977 to November 1978. The mean size of home range did not differ markedly between sexes; 136.5 m² for males and 130.8 m² for females. Home ranges of adults overlapped greatly in each sex, and the lizard was considered to be non-territorial. Individuals showed return movement to a definite area (sleeping site) within the home range, and the home range did not shift within a year or between years. Characteristics of the home range of this grassland-inhabiting lizard were discussed in relation to resource abundance and predation pressure.     

Fish communities of the upper Danube River (Germany,Austria) prior to the new Rhein-Main-Donau connection

Synopsis Ultrasonic telemetry was used to study the movement and behavior of nine adult muskellunge, 69 to 101 cm in total length. Intensive fish tracking conducted from June to August 1978 produced 1178 contacts, the basis for summer home range determinations. Eight fish established summer home ranges by the time surface water temperatures rose above 17°C in mid-June, and by early July all fish exhibited home range behavior. Individual summer home ranges were 39 to 443 ha (mean = 146 ha) in area as determined by the minimum convex polygon method, and 27 to 73 ha (mean = 63 ha) as estimated by the grid-square method. Six fish had home ranges comprised of two distinct activity centers, 2.0 to 3.5 km apart. Some home ranges spatially overlapped, but occurrences of two fish at a common location were rare. In autumn, six of eight surviving fish remained within or near their summer home ranges. Observations on these eight fish during spring and summer 1979 provided evidence of reproductive and nonreproductive homing behaviorJournal Paper No. J-11155 of the Iowa Agriculture and Home Economics Experiment Station, Ames, Iowa. Project No. 2236     

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.     

Habitat selection and home range in the Blanford's fox,Vulpes cana: compatibility with the resource dispersion hypothesis

Summary This paper presents analyses of habitat-use and home range size in the Blanford's fox. We predicted, from the resource dispersion hypothesis (RDH), that home ranges would encompass similar areas of combined fruitful habitats, but widely different areas of useless habitats, and thus that home ranges would be larger where such fruitful patches are fragmented and widely dispersed. Home range estimates of 0.5–2.0 km² were calculated for 16 adult Blanford's foxes, using three different methods. There were no significant differences in home range size between sexes or study sites. One habitat, dry creekbed, was the most frequently visited in all home ranges. Dry creekbed provided abundant prey for the foxes and only sparse cover for their predators. Both the available area of creekbed in each range, and the area of creekbed patches that was used by the foxes, were independent of home range size. However, the variance in home range size was explained by the mean distance between the main denning area and the most frequently used patches of creekbed. These results are in accord with some predictions of the resource dispersion hypothesis.     

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.     

An Examination of Scale-Dependent Resource Use by Eastern Hognose Snakes in Southcentral New Hampshire

ABSTRACT The decline of many snake populations is attributable to habitat loss, and knowledge of habitat use is critical to their conservation. Resource characteristics (e.g., relative availability of different habitat types, soils, and slopes) within a landscape are scale-dependent and may not be equal across multiple spatial scales. Thus, it is important to identify the relevant spatial scales at which resource selection occurs. We conducted a radiotelemetry study of eastern hognose snake (Heterodon platirhinos) home range size and resource use at different hierarchical spatial scales. We present the results for 8 snakes radiotracked during a 2-year study at New Boston Air Force Station (NBAFS) in southern New Hampshire, USA, where the species is listed by the state as endangered. Mean home range size (minimum convex polygon) at NBAFS (51.7 ± 14.7 ha) was similar to that reported in other parts of the species’ range. Radiotracked snakes exhibited different patterns of resource use at different spatial scales. At the landscape scale (selection of locations within the landscape), snakes overutilized old-field and forest edge habitats and underutilized forested habitats and wetlands relative to availability. At this scale, snakes also overutilized areas containing sandy loam soils and areas with lower slope (mean slope = 5.2% at snake locations vs. 6.7% at random locations). We failed to detect some of these patterns of resource use at the home range scale (i.e., within the home range). Our ability to detect resource selection by the snakes only at the landscape scale is likely the result of greater heterogeneity in macrohabitat features at the broader landscape scale. From a management perspective, future studies of habitat selection for rare species should include measurement of available habitat at spatial scales larger than the home range. We suggest that the maintenance of open early successional habitats as a component of forested landscapes will be critical for the persistence of eastern hognose snake populations in the northeastern United States.     

Ranging behavior of the Asian elephant in Sri Lanka

We studied the ranging patterns of 10 elephants in and around the Yala protected area complex, southern Sri Lanka, using VHF radio telemetry. All tracked elephants displayed similar ranging patterns. The observed home ranges were small (mean=115.2±64.0 km²) relative to reported home ranges in India, possibly in response to high habitat productivity and abundant perennial water sources. Elephants showed high fidelity to their ranges. Home ranges had relatively large core areas, suggesting intensive use of habitat. No geographically distinct seasonal ranges or migratory behavior was observed. Home range overlap was high, and territoriality was absent. Male musth ranges were considerably larger than non-musth ranges and may signify mate searching. Most elephants ranged both in and outside protected areas, suggesting that resources outside protected areas were important for their survival. Thus, translocating and restricting elephants to protected areas will be detrimental to their survival, as it limits resource access. The ranging patterns of Asian elephants suggest that conservation of the species requires their management both in and outside protected areas.     

Home ranges of brown hares in a natural salt marsh: comparisons with agricultural systems

This is the first study on spatial behaviour of brown haresLepus europaeus Pallas, 1778 based on radio-telemetry in a natural system, which we contrast with data from agricultural systems. Radio tracking took place in a Dutch salt marsh over a 10-month period, with intensive tracking sessions during April/May and December/January. Six hares could be followed in both periods and in total 1224 fixes were collected. Average home range size was calculated as 28.7±8.5 ha when using Adaptive Kernell method (Mimimum Convex Polygon: 27.3±9.0 ha) on 90% of all fixes. Such values are in the lower end of the range of those obtained for agricultural systems. Home range size did not differ between sexes, day and night, or across seasons. However, the size of the core range (50% of fixes) was twice as large in May compared to the winter period, and thus inversely related to food availability. Unlike in agricultural systems, use of space by hares did not change over the course of the season. This probably reflects the patchy nature of the natural habitat which provides food and shelter throughout the year in a confined area.     

Information-Theoretic Model Selection and Model Averaging for Closed-Population Capture-Recapture Studies

Specification of an appropriate model is critical to valid statistical inference. Given the “true model” for the data is unknown, the goal of model selection is to select a plausible approximating model that balances model bias and sampling variance. Model selection based on information criteria such as AIC or its variant AIC_c, or criteria like CAIC, has proven useful in a variety of contexts including the analysis of open-population capture-recapture data. These criteria have not been intensively evaluated for closed-population capture-recapture models, which are integer parameter models used to estimate population size (N), and there is concern that they will not perform well. To address this concern, we evaluated AIC, AIC_c, and CAIC model selection for closed-population capture-recapture models by empirically assessing the quality of inference for the population size parameter N. We found that AIC-, AIC_c-, and CAIC-selected models had smaller relative mean squared errors than randomly selected models, but that confidence interval coverage on N was poor unless unconditional variance estimates (which incorporate model uncertainty) were used to compute confidence intervals. Overall, AIC and AIC_c outperformed CAIC, and are preferred to CAIC for selection among the closed-population capture-recapture models we investigated. A model averaging approach to estimation, using AIC, AIC_c, or CAIC to estimate weights, was also investigated and proved superior to estimation using AIC-, AIC_c-, or CAIC-selected models. Our results suggested that, for model averaging, AIC or AIC_c should be favored over CAIC for estimating weights.     

Space use by Great Lakes Piping Plovers during the breeding season

ABSTRACT.   Identifying and protecting breeding habitat for imperiled species requires an understanding of the spatial and temporal movements of breeding individuals. During the 2003 and 2004 breeding seasons, we examined space use by Piping Plovers ( Charadrius melodus ) in the federally endangered Great Lakes population. We used coordinate geometry to estimate home range sizes of individual birds and examined relationships between home range size and breeding stage (incubation versus chick rearing), year, sex, number of locations, minimum plover age, distance to the nearest nest, and human beach use (high, medium, or low). The mean size of home ranges of Piping Plovers that fledged at least one chick was 2.9 ± 0.5 (SE) ha (range = 0.4–11.2 ha), and the mean linear beach distance traversed was 475 ± 53 m (range = 130–1435 m). Individuals used 3 times more beach area and 1.5 times more shoreline distance in 2003 than in 2004. Females used smaller areas than males overall and during chick rearing. Home ranges were smallest on beaches with low public use, suggesting that human disturbance may cause greater movement by individual plovers and that larger protected areas may be warranted on beaches frequented by the public to minimize disturbance to breeding birds. Our results demonstrate that nesting Great Lakes Piping Plovers occupy relatively small ranges and, therefore, that even relatively small areas of suitable habitat can have a high conservation value for this endangered population. However, the total area of habitat used varied substantially among individuals, and this should be considered when protecting habitat for the species.