Grazing behaviour of free-ranging donkeys and Shetland ponies in different reproductive states

We investigated how free-ranging mares of two species of equids (donkeys and Shetland ponies) modify their foraging behaviour to meet the increased nutritional requirements induced by lactation. We initially hypothesised that lactating mares would graze for a longer time and/or graze faster than non-lactating (dry) mares. The grazing behaviour of free-ranging animals, foraging in two low-productive dune areas, was recorded during 1 year. Results show that in both species lactating animals did not spend more time grazing than non-lactating mares. However, lactating animals took more bites, and therefore achieved a higher bite rate than dry mares. Several factors affected the differences between lactating and non-lactating animals. Lactating mares took more bites only in grassy and rough vegetations and they did this only in patches with a short sward height. In addition, lactating mares took more bites of grasses only and not of forbs or woody plants. We conclude that the extra grazing effort of the lactating animals was not distributed randomly. Lactating mares invested their extra grazing effort principally towards those items that are the most grazed by the equids in general. We propose some hypotheses to explain why lactating mares increase their bite rate instead of augmenting the time spent grazing.     

A local nearest-neighbor convex-hull construction of home ranges and utilization distributions

We describe a new method for estimating the area of home ranges and constructing utilization distributions (UDs) from spatial data. We compare our method with bivariate kernel and α-hull methods, using both randomly distributed and highly aggregated data to test the accuracy of area estimates and UD isopleth construction. The data variously contain holes, corners, and corridors linking high use areas. Our method is based on taking the union of the minimum convex polygons (MCP) associated with the k−1 nearest neighbors of each point in the data and, as such, has one free parameter k. We propose a "minimum spurious hole covering" (MSHC) rule for selecting k and interpret its application in terms of type I and type II statistical errors. Our MSHC rule provides estimates within 12% of true area values for all 5 data sets, while kernel methods are worse in all cases: in one case overestimating area by a factor of 10 and in another case underestimating area by a factor of 50. Our method also constructs much better estimates for the density isopleths of the UDs than kernel methods. The α-hull method does not lead directly to the construction of isopleths and also does not always include all points in the constructed home range. Finally we demonstrate that kernel methods, unlike our method and the α-hull method, does not converges to the true area represented by the data as the number of data points increase.     

Wide home ranges for widely foraging lizards

Space usage by animals may be influenced by a range of factors. In this study we investigate whether foraging behaviour affects the home range size of lizards. Two distinct tactics of foraging have been recognized in predators: sit-and-wait foraging (SW) and active foraging (AF). Foraging activity level of a data set of lizard species, mainly compiled from literature, is compared with their home range sizes. Two opposite predictions can be made about foraging in connection with home range area: on the one hand, SW species may exhibit larger home ranges due to their mating system; on the other hand, AF species have higher metabolic energy and thus food requirements and can be expected to have larger home ranges that have to yield this food. This study shows that percentage of the time moving (as an index of foraging mode) correlates positively with home range, even after correcting for body mass, and these patterns remain when phylogenetic relationships are taken into account. We thus conclude that home range areas parallel activity levels in lizards.     

Spider monkey home ranges: A comparison of radio telemetry and direct observation

The ranging patterns of two male and five female spider monkeys (Ateles geoffroyi) were studied with the use of radio telemetry in Santa Rosa National Park, Costa Rica. The average size of a spider monkey home range was 62.4 hectares; however, range size varied with sex, and, for females, with the presence of a dependent infant. The probability of encountering a radio-collared spider monkey in a three-hour search using radio telemetry (0.91) was much greater than using a visual search (0.20), and telemetric data resulted in a larger estimate of mean home range size than did observational data, when all subjects were compared. However, the difference appeared to be owing to the presence of male ranges in the telemetric, but not the observational, data. When the size of home ranges derived from radio-tracking data for adult females was compared to size of ranges for adult females derived from observations, the results were not significantly different. Adult males had larger home ranges than adult females, thus lending support to the hypothesis that males have adapted to the dispersion of females by occupying a large home range that overlaps the ranges of several adult females. The smallest home ranges were occupied by low-weight females with dependent infants, perhaps reflecting social and energetic constraints.     

Towards a coherent allometric framework for individual home ranges,key population patches and geographic ranges

Spatial requirements of species have often been related to body size, usually focusing on one area variable and one taxonomic group at a time. Here, we carried out a quantitative meta‐analysis and developed a minimal model, covering different types of spatial characteristics and several species groups. In a global literature review, 46 empirical regressions on home ranges and geographic ranges were collected, covering thousands of species monitored in various countries. In addition, regional data on minimum key population patches of 167 species occurring in the Netherlands were retrieved from reports. To check consistency, a theoretical model was derived from rate and density variables based on energy equivalency. The minimum number of individuals needed to sustain a viable population was considered invariant to size. According to the equations, areas were expected to scale to mass with an exponent of 1 for the individual home range and of about ¾ for the minimum population ranges. The meta‐analysis of the empirical regressions showed that average slopes for individual home ranges were between 0.74 for cold‐blooded species and 1.05 for birds and mammals. Minimum and average species geographic range scaled to mass with exponents of 1.16–1.29 and 0.28–0.46 respectively. Allometric correlations for the minimum key patch area were weak. The intercepts indicated that carnivores require more space than equally sized herbivores, while homeotherms occupy larger areas than heterotherms. Observed slopes and intercepts were often near model estimations, but important deviations from the average level were noted as well, especially for birds. Although variability was substantial in some cases, allometric approaches can contribute considerably to understanding and protecting area requirements of species.     

Hematology and serum chemistry reference ranges of free-ranging moose (Alces alces) in Norway

Baseline reference ranges of serum chemistry and hematology data can be important indicators for the status of both individuals or populations of wild animals that are affected by emerging pathogens, toxicants, or other causes of disease. Frequently, reference ranges for these values are not available for wildlife species or subspecies. We present hematologic and serum chemistry reference ranges for moose (Alces alces) adults, yearlings, and calves in Norway sampled from 1992-2000. Additionally, we demonstrated that both induction time and chase time were correlated with initial rectal temperature, although they were not significantly correlated with cortisol, aspartate aminotransferase, glucose, or creatine kinase. Overall, the reference ranges given here are similar to those given for American moose, with a few differences that can be attributed to environment, testing methodology, or subspecies or species status. This is the first report, to our knowledge, of reference ranges for moose in Norway.     

Thievery,home ranges,and nestmate recognition inEctatomma ruidum

Summary Thievery of food items among colonies of a ponerine ant,Ectatomma ruidum was common; nonnestmates in colonies or near the colony entrances receive incoming food items and carry them to their own colony. In our study area 7 of 10 colonies were victimized by thief ants. Colonies have discrete home ranges and home range size is correlated with the number of workers in the colony. Worker ants discriminate nestmates from non-nestmates when non-nestmates are presented at colony entrances, but individuals from different colonies were not observed to engage in agonistic interactions away from nest entrances. Non-nestmates gain entrance to colonies when the entrance is unguarded. Many instances of non-nestmates being removed from colonies by residents were observed. The costs and benefits of theft under these circumstances are considered.     

The ontogeny of home ranges: evidence from coral reef fishes

The concept of home ranges is fundamental to ecology. Numerous studies have quantified how home ranges scale with body size across taxa. However, these relationships are not always applicable intraspecifically. Here, we describe how the home range of an important group of reef fish, the parrotfishes, scales with body mass. With masses spanning five orders of magnitude, from the early postsettlement stage through to adulthood, we find no evidence of a response to predation risk, dietary shifts or sex change on home range expansion rates. Instead, we document a distinct ontogenetic shift in home range expansion with sexual maturity. Juvenile parrotfishes displayed rapid home range growth until reaching approximately 100–150 mm length. Thereafter, the relationship between home range and mass broke down. This shift reflected changes in colour patterns, social status and reproductive behaviour associated with the transition to adult stages. While there is a clear relationship between body mass and home ranges among adult individuals of different species, it does not appear to be applicable to size changes within species. Ontogenetic changes in parrotfishes do not follow expected mass–area scaling relationships.     

Long-term changes in the winter home ranges of Japanese monkeys in the Shiga heights

In the home ranges of the monkeys, the densely utilized food sites (densely utilized sites of food resources ofWada andTokida, 1981) varied over a period of ten years. The Shiga B₂ troop changed both its densely utilized food sites and the kinds of tree mostly eaten within the same home range, whereas the Shiga C troop transferred to a new home range. The home range transition of the C troop was influenced by both food deficiencies and the existence of the B₂ troop. Based on these facts, it can be said that two types of long-term home range utilization were distinguishable.     

Seasonal home ranges and fidelity to breeding sites among ringed seals

Population structure and patterns of habitat use among ringed seals (Phoca hispida) are poorly known, in part because seasonal movements have not been adequately documented. We monitored the movements of 98 ringed seals in the Beaufort and Chukchi seas between 1990 and 2006 using three forms of telemetry. In the winter—spring period (when the seals were occupying shorefast ice), we used radio and ultra-sonic tags to track movements above and below the ice, respectively. We used satellite-linked transmitters in summer and fall (when the seals ranged away from their winter sites) to track at-sea movements. In the shorefast ice habitat, the home ranges of 27 adult males ranged from <1 to 13.9 km² (median = 0.628) while the home ranges of 28 adult females ranged from <1 to 27.9 km² (median = 0.652). The 3-dimensional volumes used by 9 seals tracked acoustically under the ice averaged 0.07 (SD = 0.04) km³ for subadults and adult males and 0.13 (SD = 0.04) km³ for adult females. Three of the radio-tracked seals and 9 tracked by satellite ranged up to 1,800 km from their winter/spring home ranges in summer but returned to the same small (1–2 km²) sites during the ice-bound months in the following year. The restricted movements of ringed seals during the ice-bound season—including the breeding season—limits their foraging activities for most of the year and may minimize gene flow within the species.     

Male Corncrakes Crex crex extend their home ranges by visiting the territories of neighbouring males

Capsule Radiotracked male Corncrake often intruded on the territories of neighbouring males.

Aims To test that intruders' visits are goal-directed, not just a by-product of extended spatial activity during daylight hours.

Methods Using radiotelemetry, we sampled a total of 20 three-day home ranges from 11 tagged males. We recorded daily vocal activity and used a permutation test to see if the movements of tracked males were independent of the position of neighbouring males.

Results The majority of males who had a neighbouring male, up to approximately 600 m from their night calling site, undertook goal-directed visits to the neighbour's territory. Males undertook these visits every day, or every other day, when the neighbours were close. Males undertook visits approximately once every three days when they were more distant. The time spent in the neighbour's territory was longest where the distance between night calling sites was about 200 m. Males tended to be silent in neighbour's territory, apparently to prevent confrontation. Otherwise the distance of neighbouring males did not significantly affect daytime vocal activity. Visiting males tended to sing more often in their home territories.

Conclusions Daily movement of the majority of males was towards the neighbouring male's calling site. We suggest that the purpose of these visits was to seek females. These males may try to drive a female into their territory or gain extra-pair copulation.     

LoCoH: nonparameteric kernel methods for constructing home ranges and utilization distributions

Parametric kernel methods currently dominate the literature regarding the construction of animal home ranges (HRs) and utilization distributions (UDs). These methods frequently fail to capture the kinds of hard boundaries common to many natural systems. Recently a local convex hull (LoCoH) nonparametric kernel method, which generalizes the minimum convex polygon (MCP) method, was shown to be more appropriate than parametric kernel methods for constructing HRs and UDs, because of its ability to identify hard boundaries (e.g., rivers, cliff edges) and convergence to the true distribution as sample size increases. Here we extend the LoCoH in two ways: "fixed sphere-of-influence," or r-LoCoH (kernels constructed from all points within a fixed radius r of each reference point), and an "adaptive sphere-of-influence," or a-LoCoH (kernels constructed from all points within a radius a such that the distances of all points within the radius to the reference point sum to a value less than or equal to a), and compare them to the original "fixed-number-of-points," or k-LoCoH (all kernels constructed from k-1 nearest neighbors of root points). We also compare these nonparametric LoCoH to parametric kernel methods using manufactured data and data collected from GPS collars on African buffalo in the Kruger National Park, South Africa. Our results demonstrate that LoCoH methods are superior to parametric kernel methods in estimating areas used by animals, excluding unused areas (holes) and, generally, in constructing UDs and HRs arising from the movement of animals influenced by hard boundaries and irregular structures (e.g., rocky outcrops). We also demonstrate that a-LoCoH is generally superior to k- and r-LoCoH (with software for all three methods available at http://locoh.cnr.berkeley.edu).     

Alternative strategies in the acquisition of home ranges by male pine martens in a high-density population

Two strategies of home range acquisition by male subadult pine martens (Martes martes) were described from a high-density population inhabiting Bia?owie?a National Park. Four mother?Coffspring pairs were identified by genetic parentage assignments. Four subadult males showed two different strategies of home range acquisition: dispersal and sedentary. The dispersing males used an area 4?C10 times larger than in sedentary subadult males. A sedentary subadult male used his natal area with his mother, and in the following mating season, this male left this area and established a home range that overlapped greatly with another unrelated female near the natal range. A similar high overlap between another subadult male and an unrelated adult female persisted for 3?years. After the death of this female, the male extended his range to overlap slightly with two to four other females. The sedentary strategy adopted by some subadult males may explain the great variation in spacing patterns of solitary mammals.     

Spatial colonization by feral domestic catsFelis catus of former wildcatFelis silvestris silvestris home ranges

Presently, wildcatFelis silvestris silvestris Schreber, 1777 populations are fragmented and rapidly declining in most of Europe. Although habitat destruction possibly constitutes the most serious threat to wildcat survival, hybridisation with feral domestic cats is also a critical problem. However, the mechanisms that allow domestic cats to colonise former wild cat home ranges are yet unclear. The present paper describes the decrease of typical phenotypic wildcats and the increase of phenotypic domestic cats in a remote wild area of Portugal (Serra da Malcata). A field survey using box-traps and radio-tracking between 1998 and 2001 revealed that wildcats were widespread in the study area and no domestic cats were present. A second survey using camera traps between 2005 and 2007 revealed only one wildcat whereas four typical domestic phenotype individuals were photographed. The present study clearly emphasizes the need for urgent measures aimed at preserving wildcat populations. These measures should include a national census of the species and an extensive monitoring of genetic integrity of wildcat populations, followed by the elaboration of a wildcat conservation action plan.