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We examined space use by female gray-tailed voies Microtus canicaudus (Miller, 1897) and recruitment of juveniles in response to relative abundance of food and increased intruder pressure following experimental removal of habitat. Our experiment indirectly tested the assumptions of the food-defense and pup-defense hypotheses for female territoriality. Following a 70% reduction in habitat, territories of females shrunk from -50 m to < 20 m with no significant difference in pregnancy rates or overall juvenile recruitment compared to controls. Juvenile recruitment was not adver­sely affected by overall density or the numbers of males sharing a patch, but decreased significantly as the number of unrelated adult females sharing a patch increased. We did not measure infanticide directly, but the decreased rate of juvenile recruitment in the presence of adult females but not males suggests that pup mortality rather than food limitation contributed to reduced juvenile recruitment, We conclude that at high densities, increased intruder pressure from adult females had a greater impact on juvenile recruitment than did food abundance. Thus, our results suggest that patterns of space use, reproductive rates, and juvenile recruitment were more consist­ent with the pup-defense than the food-defense hypothesis for female territoriality.
Activity, spatial ecology, and pattern of sett use of a mediterranean population of badgers Meles meles Linnaeus, 1758 are described. Data come from Doñana National Park (SW Spain) where a 1-year radio-tracking study and a 9-year capture-recapture study were carried out. Badger home ranges were spatially structured, territories having an average size that is the largest reported in the literature. There was a correlation between territory size and ecological variables reflecting food patch dispersion. It is suggested that badgers might set territory limits to include enough patches of rabbit burrows in the critical summer period of low rabbit abundance. Badgers were not strictly nocturnal, and showed decreased activity levels in winter. Activity levels were higher in badgers living in dry habitats, and in all badgers during the dry season. Both photoperiod and rabbit availability were suggested as factors influencing activity parameters like activity length or resting intervals during activity periods. Differences in the pattern of use of the main and secondary setts were found between reproductive females and other individuals.
In mosaics of forest environment the bank vole Clethrionomys glareolus {Schreber, 1780) prefers patches with dense vegetal cover like understorey or tail herbaceous plants, like ferns or sedges. The size and intensity of the space use, the rate of colonization of free space with population increases and mean home range size are highest in habitats, or their parts, covered uniformly by this type of vegetation. Habitats with dense and uniform understorey characteristically support high vole densities, high numbers of sexually active individuals, high survival rates of indi­viduals entering the population at the beginning of the reproductive season, a high emigration during the second half of the season and a low immigration. Voie popu­lations in habitats of poor and clumped understorey are characterized by low densities, high immigration of individuals entering to the population during the second half of the season and a high turnover of individuals. It has been suggested that vole distribu­tion in a mosaic of forest habitats depends upon the abundance of structural elements of the habitat that may serve as defensive structures against predators.
The ranges and space use of eight radio-tracked Spanish Imperial Eagles are described. The annual mean range was 25 146 ha during the breeding season (BS) and 20 557 ha in the non-breeding season (NBS). The eagles were found up to 35.9 km away from their nest during BS and nearly 62 km away during NBS. The maximum total distance covered in one day was 113.6 km, with males flying longer distances than females during BS. There was less overlap between ranges during BS, and the mean home range varied from 3881 ha in BS to 2085 ha in NBS. The areas where territorial behaviour (display flights, defence and/or aggression) was observed contained the nest-tree, the most frequently used perches, and the feeding ground nearest to the nest. Breeding home ranges were negatively correlated with densities of Rabbits Oryctolagus cuniculus. Breeding eagles whose home range had low rabbit densities travelled 16.2-28.9 km from their nest to reach distant, undefended feeding grounds with much higher rabbit densities. Our results suggest that home ranges varied with prey density and a bird's reproductive status. Larger breeding ranges are probably related to an increase in energy requirements, while habitat quality is probably a regulatory mechanism of space use. In terms of home range analysis methodology, our observations of eagle behaviour favour Cluster Analysis over Kernel, particularly for defining distant feeding grounds.
Home range size and overlap ofCalomys musculinus (Thomas, 1913) was examined in relation to sex and breeding periods. The study was carried out in four 0.25 ha enclosures, in a natural pasture, between October 2002 and July 2003. The four enclosures functioned as independent populations and each was considered a replicate. The capture, mark and recapture method was used. Home range size and overlap inC. musculinus depended on sex and period. Home range size of males was always larger than that of females. Females showed a small degree of intra-sexual home range overlap during the breeding period. In general, male home ranges overlapped with females. We conclude that differences in home range size inC. musculinus is determined by sex and breeding period. Moreover, the degree of inter- and intra-sexual home range overlap during the breeding period suggests that both males and females ofC. musculinus use space differently. Females did not share their home range with other females, while males fully shared it with both sexes, and male spacing is influenced by the distribution of females. A promiscuous-polygynous mating system is suggested forC. musculinus.
Density and distribution of the bank vole Clethrionomys gtareolus (Schreber, 1780) was studied in 1986-1989 on two forest plots (one of 5.4 and one of 5.8 ha) that differed with respect to their mosaic character. On both plots densities of bank voles were similar in different habitats. The same trap sites were used by voles in a similar way in successive study years. Spatial variations in habitat use were primarily related to the density of plant cover and its spatial distribution providing shelter from predators. Frequency and intensity of use of trap sites by voles was positively corre­lated with the percent cover of shrubs and tall herbaceous plants. It was negatively correlated with the percent area without herb cover and with the percent cover of photophilous herbs. Using the correlation method, it was possible to estimate the effect of a given environmental factor on the distribution of bank voles only when the range of spatial variation of this factor was large.
Radiotracking of three couples of polecats Mustela putorius Linnaeus, 1758 in wetlands of western France showed that the monthly home ranges of male averaged 0.426 km2 and overlapped the females' ranges which were smaller (0.125 km2). Although the distribution of polecat's localizations in the three main habitats differed significantly between the male and the female, the seasonal overlap of habitat niches (Cjk) was considerable and varied from 0.727 to 0.894. The proportion of simultaneous localizations on the same square averaged 4% of monthly localizations while 96% of the localizations indicated solitary activity. Also, the duration of time occuring together was short: only 1.8 days per month on average. The observations suggested that the social organization of M. putorius was characterized by periodic variations of intra- specific tolerance between males and females which were probably influenced by hormonal factors during spring and by food availability during summer and autumn. A strong spatio-temporal segregation, however, determined a particularly individual exploitation of the space.
In 2005–2008, we radio-tracked 17 foxes in rural areas of Southern Germany. The mean home range size was 76.6 ha (95% MCP) or 138.9 ha (95% fixed kernel), and the built-up area formed an integral part of the home range. Home ranges of juvenile foxes were significantly smaller than home ranges of adult foxes. Gender-specific differences among adult foxes were not established. A minimum population density of 2.7 foxes per km2 and summer densities of up to 13.4 foxes per km2 were calculated. Therefore, the fox density was three to eight times higher than that of strictly rural foxes. Daytime resting sites of foxes were mostly found in forests (62.2%) and reedbed areas (20.6%). Of the resting sites, 14.8% were situated inside settlements, in fallow gardens or gardens of residents. During the day, foxes exhibited habitat preferences for forests and reedbed areas. A habitat structure that offers plenty of cover or dense vegetation is essential for its selection as a safe resting site. If this basic requirement is fulfilled, foxes also choose resting sites within settlements, and are not disturbed by human presence.
The development of each town brings about the necessity to change the way of the иве of surrounding areas and the town centre area, the structure of which becomes burdensome and badlyfitting. Every now and again in the development of every town it becomes necessary to subdue this difficulty through an application of various actions setting in order and adjusting the way of area utilization to the function currently indispensable from the view­point of proper organization and function of a town. Such action sare usually referred to as land readjustment or land redevelopment. They include a set of rural land development steps, which may be successfully used in suburban areas (in transitional zone) having still some traits of agricultural nature.
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