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A link between dental abnormalities and loss of genetic variation has been reported for unconfined populations of American bison Bison bison (Linnaeus, 1758) but not for captive populations. From a zoo herd with a small founder population and likely history of inbreeding, we report the first recorded occurrence of dental abnormalities in captive bison and the first case of supernumerary second premolars in bison.
Based on the analysis of the cytb gene of mtDNA the taxonomic position was determined of two closely related Bovidae species: American bison (Bison bison) and European bison (Bison bonasus). Reference sequences were determined for both species. In the American bison two variants of cytb gene were identified. Both of them are novel sequences, so far not published in GenBank. For comparison the reference sequences in four another representatives of Bovidae (Polish Red cattle, Zebu cattle, Merino sheep and Polish White Improved goat) were determined. Phylogenetic reconstructions were obtained by the neighbour-joining method (N-J) on all mutations and on changes with removed mutations In third position. Topology of phylogenetic trees showed that American bison and European bison form a separate nodes. The molecular data presented corroborate the results of earlier studies showing that although the two species in question are very closely related, their classification as subspecies is rather questionable. The fact that nodes for American as well as European bison show relatively high bootstrap scores supports this hypothesis.
We characterized social and spatial patterns of wallowing (dust-bathing) behavior in an American bison Bison bison (Linnaeus, 1758) population on a tallgrass prairie site in Oklahoma, USA. Consistent with earlier studies, wallowing was primarily practiced by adults, Unlike earlier studies, however, aggressive interactions associated with wallowing incidents were rare, probably due to the reduced bullicow ratio in the population. Forty-three significant soil disturbance sites, known as wallows, were created by wallowing activity during the 2-year study. The spatial distribution of wallows was significantly different from overall bison habitat use patterns for some landscape characteristics. Bison preferentially formed wallows on relatively level areas on spring and fall burns, thus avoiding summer burns, unburned areas, and severe slopes. Bison wallowed exclusively on bare or exposed soils when not using wallows, and in many instances wallowed on soil disturbed by other animals. When coupled with a preference for wallowing on relatively coarse soils, bison clearly exhibit a macro- and microsite preference for the conduction of this behavior. This preference has important implications for wallow distribution and their resulting ecological function in prairie environments.
The aim of the study was to evaluate the level of intestinal parasitic infection in bison (Bison bison L.) in a private farm located in southern Poland. The prevalence of infection [%] and the faecal oocyst/egg output in OPG (oocysts per gram) and EPG (eggs per gram) were estimated on the basis of coproscopic examination. The results showed a high occurrence of coccidia (Eimeria spp.) – 68.2% (347 OPG), as well as nematodes – 65.9% (93 EPG), with the Nematodirus genus observed in 6.8% of the animals examined. Among other nematodes, Toxocara (Neoascaris) vitulorum was found in 6.1% (10 EPG) of the animals. Trichuris ovis and Strongyloides papillosus occurred rarely (0.8%). Tapeworms, Moniezia spp., were noted in 9.1% of the animals. The primary factor conducive to the spread of gastrointestinal parasitic infections in the herd were wet pastures created in dried fish ponds, where protozoan oocysts and helminth eggs had excellent conditions for development and infection. The small number of large quarters prevented their frequent rotation, which promoted the accumulation of parasites in all developmental stages in the environment and quick reinfection. Feeding animals directly from the ground may also promote infection. A single deworming procedure per year appears to be insufficient.
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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