Consistency and change in bank vole (Clethrionomys glareolus) home ranges across a decade

1998 ◽  
Vol 76 (7) ◽  
pp. 1329-1334 ◽  
Author(s):  
A Fredric Karlsson ◽  
Eugene R Potapov
Keyword(s):  
Home Range ◽  
Snow Cover ◽  
Bank Vole ◽  
Snow Depth ◽  
Clethrionomys Glareolus ◽  
Home Ranges ◽  
Partial Explanation ◽  
Mating Period ◽  
Bank Voles ◽  
Significant Difference

Minimum distance moved (MDM) and home-range sizes were studied in overwintering bank voles (Clethrionomys glareolus) during March and April in 1985, 1986, and 1996 near Uppsala, Sweden. In 1985 and 1986, the average snow depth was 50 and 35 cm in March and 7 and 18 cm in April, respectively. In 1996 the snow depth was only 16 cm in March and 2 cm in April. Bank voles were found to have winter nests at exactly the same grid coordinates in 1985, 1986, and 1996. Among females there was a high degree of consistency in home-range sizes, both between months and between years. Daily MDM of females was shorter in March 1996 than in 1985 and 1986, while no significant difference occurred during April. Males' home-range sizes, on the other hand, increased significantly from March to April in all 3 years, i.e., at the onset of the mating period. There was no significant difference in males' home-range sizes in March across years, but in April, home ranges were significantly larger 1985 and 1986 than in 1996. Males' average home-range sizes in April showed a positive correlation with snow depth. MDM of males in both March and April was also significantly higher during the snowy years of 1985 and 1986 than in 1996, when there was much less snow. These observations suggest that adequate snow cover is a favourable factor, allowing the males to expand their home ranges, while lack of snow or a thin, patchy snow cover prevents them from travelling longer distances during the mating period and consequently from visiting a large number of potential mates. These differences in the behaviour of male bank voles between snow-rich and snow-poor years may offer a partial explanation of the hypothetical connection between the less severe winter conditions during the past decade and the decline in population density and cyclicity in boreal bank vole populations.

Home range of the allied rock-wallaby, Petrogale assimilis

1994 ◽  
Vol 21 (1) ◽  
pp. 65 ◽  
Author(s):  
A Horsup
Keyword(s):  
Home Range ◽  
Major Effect ◽  
Home Range Size ◽  
Home Ranges ◽  
Temporal Separation ◽  
Dry Tropics ◽  
Shelter Site ◽  
Significant Difference ◽  
Mean Size ◽  
Core Areas

The home range and movements of the allied rock wallaby, Petrogale assimilis, a small macropod of the seasonally wet-dry tropics of Queensland, were studied over a 22-month period. There was no significant difference in the size of home ranges (95% isopleth) or core areas (65% isopleth) of males and females. Home ranges were generally elliptical with a mean size of 11.9 ha. Season had a major effect on home ranges. The following measures were all significantly greater in the dry seasons than in the wet seasons: home-range size (larger), home-range shape (more elongate), distance moved by females when feeding (longer), distance between shelter site and home-range centre of activity (longer). Feeding movements of males did not vary seasonally and were as long as dry-season movements of females, suggesting that movements of males are primarily determined by behavioural rather than physiological considerations. The overlap of rock-wallaby home ranges varied little between the sexes or seasons and averaged 38%. Core areas overlapped by an average of 22%; however, feeding adult rock-wallabies rarely met other conspecifics, except their partners. A comparison of the fixes of unpaired wallabies that had overlapping home ranges showed that temporal separation was occurring. In contrast, the home ranges of consort pairs showed extremely high temporal and spatial overlap. Rock-wallabies exhibited strong fidelity to their home ranges. The overlap of the seasonal home ranges and core areas of each individual rock wallaby averaged 68% and 52%, respectively. However, the seasonal home range of a socially immature adult male altered in location and size as he matured socially until it stabilised when he obtained a permanent consort.

Adrenal growth during pregnancy in the bank vole, Clethrionomys glareolus: initiation by mating

1980 ◽  
Vol 58 (8) ◽  
pp. 1458-1461
Author(s):  
Torgny O. Gustafsson ◽  
C. Bertil Andersson
Keyword(s):  
Bank Vole ◽  
Ovarian Hormones ◽  
Clethrionomys Glareolus ◽  
Adrenal Weight ◽  
Induced Ovulation ◽  
Bank Voles

The relative roles of mating and the ovary in the initiating of adrenal growth in pregnant bank voles, Clethrionomys glareolus, were studied. In one experiment females were ovariectomized shortly after mating; 4 days later they had significantly heavier adrenals than unmated, ovariectomized controls. In another experiment females were ovariectomized and brought into oestrus by oestradiol- 17β injections. Half of the females were mated and after 4 days their adrenals were significantly larger than those of unmated controls. We conclude that the increase in adrenal weight during pregnancy in bank voles is triggered directly by mating, without involvement of ovarian hormones. The mechanism is suggested to be a neuroendocrine reflex, acting via the hypothalamus and the pituitary. The mechanism may be the same as that involved in the induced ovulation in this species.

Initiation of breeding after winter in bank voles: effects of food and population density

2001 ◽  
Vol 79 (10) ◽  
pp. 1743-1753 ◽  
Author(s):  
Jana A Eccard ◽  
Hannu Ylönen
Keyword(s):  
Population Density ◽  
Bank Vole ◽  
Local Density ◽  
Local Population ◽  
Food Supplements ◽  
Clethrionomys Glareolus ◽  
Environmental Stability ◽  
Food Treatment ◽  
Bank Voles ◽  
Winter Food

We studied factors causing variation in the initiation of reproduction after winter in the bank vole (Clethrionomys glareolus), an iteroparous seasonal breeder, by offering different winter food supplements and monitoring local density variation. We used either sunflower seeds or barley to supplement the diet of populations of bank voles in grassland enclosures. In a parallel experiment we used spruce seeds, a natural winter food, to supplement the diet of bank vole populations in unfenced spruce forest. Survival, maturation, and breeding were monitored by livetrapping. Population density decreased during winter in grassland enclosures and remained constant in the forest, with no difference between food treatments. Breeding was initiated earlier in the grassland enclosures than in the forest, probably because of the supplemental food supply in both seed treatments and social and environmental stability in enclosures. Within both experiments, we found no differences in timing of parturition between food treatments. Inter actions of food treatment with density of females influenced the time of initiation of breeding in both experiments. At low densities, breeding started up to 1 month earlier than the population average. At high densities, a proportion of females did not breed during spring. Massive food supplements advanced the initiation of breeding, but among animals with similar food supplies, local population density seemed to have stronger regulatory effects. Local density variations may therefore create asynchronous breeding patterns within populations under similar wintering conditions.

Home range, movement and habitat utilisation of the Carpentarian rock-rat (Zyzomys palatalis) in an isolated habitat patch

2004 ◽  
Vol 31 (3) ◽  
pp. 327 ◽  
Author(s):  
Helen Puckey ◽  
Milton Lewis ◽  
David Hooper ◽  
Carrie Michell
Keyword(s):  
Home Range ◽  
Radio Telemetry ◽  
Central Area ◽  
Limited Resource ◽  
Home Ranges ◽  
Habitat Patch ◽  
Minimum Convex Polygon ◽  
Significant Difference ◽  
Core Areas ◽  
The Mean

Radio-telemetry was used to examine the home range, movement and habitat utilisation of the critically endangered Carpentarian rock-rat (Zyzomys palatalis) in an isolated habitat patch in the Gulf of Carpentaria hinterland over a 13-month period. Two home-range estimators were used in the study, (i) minimum convex polygon (MCP) and (ii) fixed Kernel (KL), the latter also being used to estimate core areas of activity. Based on a total sample size of 21 individuals, the mean MCP home range was 11 165 m2, similar to the mean KL home range of 10 687 m2. Core areas were, on average, 11.9% of the KL home-range estimate. There was no significant difference in the size of home range or core area of males and females. Juveniles had a significantly smaller home range than adults. Home ranges and, to a lesser degree, core areas were non-exclusive, with multiple areas of overlap (averaging 41% and 38% respectively) within and between all age and gender categories, but especially between males and between juveniles. Movement frequencies showed that animals made many short forays in a central area close to the arithmetic home-range mean and far fewer long forays of distances greater than 100 m from the central area. The spatial and temporal activity of Z. palatalis was concentrated in, but not confined to, the 'valley' and 'slope' habitats, with fewer movements of rats onto the surrounding 'plateau'. Resource selection analyses showed that Z. palatalis tended to prefer valley and slope habitats over the plateau and that the proportion of point locations was significantly higher for adults in the slope habitat and for juveniles in the valley habitat. Most home ranges were centred on the ecotone between these two habitat types. Although isolated and spatially limited, these habitat patches provide high-quality resources for dense populations of Z. palatalis. This study exemplifies a species' attempt to make efficient use of a limited resource in an otherwise hostile environment. Even small declines in habitat area or quality due to their vulnerability to fire would impact upon many animals.

scholarly journals Annual vs. Multiple-Year Home Range Sizes of Individual Blanding's Turtles, Emydoidea blandingii, in Central Wisconsin

2008 ◽  
Vol 122 (1) ◽  
pp. 61 ◽  
Author(s):  
Matthew Schuler ◽  
Richard P. Thiel
Keyword(s):  
Home Range ◽  
Space Use ◽  
Home Range Size ◽  
Range Size ◽  
Home Ranges ◽  
Convex Polygons ◽  
Short Term ◽  
Emydoidea Blandingii ◽  
Significant Difference ◽  
Short Time

Most studies of home ranges occur over short time periods and may not represent the spacial requirements of long-lived organisms such as turtles. Home ranges of 18 individual Blanding’s Turtles (Emydoidea blandingii) were measured using minimum convex polygons. Annual space use was compared to multi-year space use by individual turtles. We found a significant difference between annual home range size (25.5 hectares) and multi-year (two to six years) home range size (65.7 hectares; n = 18, P = 0.016). Caution should be employed when making management decisions based on short-term studies of long lived species.

Younger bank voles are more vulnerable to avian predation

2008 ◽  
Vol 86 (9) ◽  
pp. 1074-1078 ◽  
Author(s):  
Taru Meri ◽  
Matti Halonen ◽  
Tapio Mappes ◽  
Jukka Suhonen
Keyword(s):  
Sex Ratio ◽  
Clethrionomys Glareolus ◽  
Selective Predation ◽  
Field Sample ◽  
Avian Predator ◽  
Avian Predation ◽  
Bank Voles ◽  
Significant Difference ◽  
Total Impact ◽  
Selection Of

The importance of predation on prey populations is mainly determined by the number of eaten prey. However, the total impact of predation might also be determined by the selection of certain prey individuals, e.g., different sexes or age categories. Here we tested selective predation by an avian predator, the pygmy owl ( Glaucidium passerinum (L., 1758)), on bank voles ( Myodes ( Clethrionomys ) glareolus (Schreber, 1780)). We compared the sex, age, and mass of hoarded prey with the animals snap-trapped from the field. There were no differences in the sex ratio between hoarded bank voles and those available in the field. However, hoarded voles were significantly younger than ones in the field sample. There was no statistically significant difference in mass between animals from larders and from the field. We suggest that the greater vulnerability of younger animals to predation might be due to their higher activity, or alternatively, they might be forced to forage in less safe habitats.

Home-range and den use of the mahogany glider, Petaurus gracilis

2000 ◽  
Vol 27 (1) ◽  
pp. 49 ◽  
Author(s):  
Stephen M. Jackson
Keyword(s):  
Home Range ◽  
Dry Season ◽  
Home Ranges ◽  
Adjacent Area ◽  
Wet Season ◽  
Male And Female ◽  
Fragmented Habitat ◽  
Significant Difference ◽  
Socially Monogamous ◽  
Males And Females

The home-range of the mahogany glider was estimated, and its social behaviour examined, by following radio-collared animals over a two-year period within an area of continuous habitat and an adjacent area of fragmented habitat. The average home range within the continuous habitat was 19.25 ha for males and 20.34 ha for females, with male and female pairs occupying a combined area of 23.15 ha. In contrast, the average home range in the fragmented habitat was 11.05 ha for males and 6.80 ha for females, with a combined home-range of male and female pairs being 11.60 ha. The average overlap of the home ranges of paired males and females was 85.9%, compared with approximately 11% for non-paired individuals, which suggests that mahogany gliders are socially monogamous. For a total of 46 nights on which gliders were considered to behave normally for the entire night, the average foraging distance was 1506 m (range 590–3420 m) with no significant difference between males and females in either the continuous or fragmented habitat. There was, however, a significant difference in the distance individuals travelled during different times of the year, with longer distances being travelled during late dry season/wet season and shorter distances during the early to mid dry season. Mahogany gliders also travelled further when there was a high availability of nectar and pollen than when there was lower availability. A total of 83 dens (tree hollows) were recorded for the mahogany glider, with the poplar gum, Eucalyptus platyphylla, forest red gum, Eucalyptus tereticornis, and Clarkson's bloodwood, Corymbia clarksoniana, being most used.

Sterile matings initiate the breeding season in the bank vole, Clethrionomys glareolus. A field and laboratory study

1982 ◽  
Vol 60 (3) ◽  
pp. 387-391 ◽  
Author(s):  
Lilian M. Westlin ◽  
Erik Nyholm
Keyword(s):  
Male Sterility ◽  
Breeding Season ◽  
Laboratory Study ◽  
Bank Vole ◽  
Laboratory Experiments ◽  
Clethrionomys Glareolus ◽  
Bank Voles ◽  
Young Of The Year

The start of the breeding season of overwintered female bank voles, Clethrionomys glareolus, and also the start of breeding in young of the year, was characterized by a general occurrence of sterile ovulations. Similarly, in laboratory experiments, 23 out of 42 young virgin females failed to become pregnant after the first mating, and often mated several times before becoming pregnant. The experiments indicated that the sterile ovulations were attributed to temporary sterility of the females during maturation either at adolescence or at the beginning of the new breeding season, and not a result of (1) initial ovulations of the season being spontaneous, (2) male sterility, or (3) male-induced pregnancy blockage.

Eimeria-parasites are associated with a lowered mother's and offspring's body condition in island and mainland populations of the bank vole

Parasitology ◽  
2006 ◽  
Vol 134 (1) ◽  
pp. 23-31 ◽  
Author(s):  
H. HAKKARAINEN ◽  
E. HUHTA ◽  
E. KOSKELA ◽  
T. MAPPES ◽  
T. SOVERI ◽  
...  
Keyword(s):  
Body Condition ◽  
Bank Vole ◽  
Important Variable ◽  
Host Population ◽  
Significant Loss ◽  
The Body ◽  
Clethrionomys Glareolus ◽  
Vole Population ◽  
Isolated Populations ◽  
Bank Voles

This study, based on correlative data, tests the hypothesis that infections withEimeriaspp. parasites exert a significant loss of fitness of bank voles (Clethrionomys glareolus) reflected in lower reproductive success and survival, declining host population densities and are associated positively with population size. The study was conducted in 20 mainland and 27 island populations in central Finland during May–September in 1999. Faecal samples showed that 28% of 767 individuals were infected withEimeriaspp. The presence ofEimeriaparasites was higher in dense mainland populations than in sparsely populated islands. Eimerian infections increased during the course of the breeding season, probably as a result of the high infection rate of young individuals. Accordingly, the body masses of bank voles were negatively related to the presence ofEimeriaspp. Reproductive output, as measured by the breeding probability of females and litter size, was not associated with the presence of eimerian infection. Interestingly, the body condition of the infected mothers appeared to be low. Moreover, mother's body condition was the single most important variable studied that showed a positive correlation to pup's body condition at birth. On small islands ([les ]3·2 ha) that were comprehensively trapped, the mean number ofEimeriaspp. in the bank vole population was negatively related to density changes of the bank vole population during the study. Our data are consistent with the idea that infection with coccidian parasites may be one of the factors responsible for declining host populations in small, isolated populations.

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