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The determination of the age composition of a population is considered to be a fundamental parameter for the analysis of life-history strategy of the species. In the Tayassuidae, the determination of relative age has been primarily based on molar tooth wear, sometimes combined with other external characteristics, such as hair color or body size. The present study examined the dental composition of white-lipped peccariesTayassu pecari (Link, 1795) . Through the determination of the erupted dental pattern and its relation to the body weight of the animal, six age classes were established. The presence of molar teeth was considered the most accurate parameter for establishing age classes for white-lipped peccaries.
The two semi-aquatic shrew species Neomys fodiens and Neomys anomalus are very similar in their ecology and morphology. Thus, they tend to be strong competitors for resources when they occur syntopically in habitats. We analysed the microhabitat selection of both species based on 14 parameters at two study sites in western Saxony (Germany). At the first study site, the results show segregation into different preferred microhabitats. In comparison to N. fodiens, N. anomalus occurred in low distance to the oxbow lake at places with denser herbal cover. Thus, we verified the hypothesis of Rychlik (Acta Theriologica 42:351-388 1997) who assumed differences in microhabitat niches for both shrew species to avoid competition. Furthermore, there was a spatial segregation within N. fodiens depending on their age. While adults occurred close to the water at areas with sparse herb layer, the juveniles and subadults were predominantly captured in some distance to the stream at denser vegetation. We assume that this is the result of different microhabitat preferences in N. fodiens depending on age and not a result of intraspecific antagonism. Moreover, the possibility to build subsurface burrows (and as an equivalent to this, crevice systems resulting of bank fixation with large stones) seems to be the main limiting factor for the occurrence of N. fodiens at the other surveyed site. At this site, no differences in microhabitats were visible between the age classes of N. fodiens.
This paper presents the results of investigation into the variability of the share of heartwood on the stem cross-section of Douglas fir in Poland. The research was conducted in Douglas fir stands in the IV and V age classes. The feature was analysed on increment cores taken from the trees at 1.3 m level from the base of the stem, in the N and S direction. The differences of the share of heartwood between Douglas firs of the V and VI age classes as well as between the trees growing in moderate and broken crown closure were not significant. No significant differences occurred between specimens of different vitality, either; however, the trend towards increasing the share of heartwood in weak trees with relation to normal and lush ones was noticeable. No significant correlations between the share of heartwood and crown parameters were noted. Three regions were distinguished in the territory of Poland: the southern and north-western ones, where Douglas firs have a higher share of heartwood on the stem cross-section, and the central-western one, where the share is lower.
We studied the variation of linear measurements and skull capacity in Lowland European bisonBison bonasus bonasus (Linnaeus, 1758) during postnatal development, and the dependencies of the parameters in relation to sex, age, and body mass of the animals. Material consisted of 599 bison skulls (310 males and 289 females), within the age range of 1 month to 21 years (males) and to 27 years (females). In the group of calves to 1 year old, no sex connected differences in skull measurements were observed, whereas the skull capacity in older calves was significantly larger (0.01>p>0.001) in males than in females. From the third year of life, most skull measurements display characteristics of sexual dimorphism. Skull development in both sexes is most intensive during the first three years of life, and slows from the age of 5. In older individuals of both sexes (≥ 6 years), orbital breadth continues growing and, in females, breadth of splanchnocranium continues increasing. Growth in a bison’s skull capacity is most intensive up to the third year of life and slows from the age of 5. During postnatal development, a bison skull grows proportionally except the neurocranium, which grows slightly slower in comparison with basal length and its development finishes earlier than that of splanchnocranium. In ontogenesis, a bison skull grows much slower compared to body mass. In relation to body mass, skull capacity and the height of neurocranium grow most slowly while orbital breadth grows most intensively. The results obtained were compared with data on skull sizes of bison born in 1930–1950 and bred in captivity and with skulls of the American bisonBison bison. Inbreeding is probably responsible for some types of phenotypic abnormalities in the skull which appear in modern European bison.
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