940 resultados para Esrom, Denmark (Cistercian monastery)


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This study compares associations between demographic profiles, long bone lengths, bone mineral content, and frequencies of stress indicators in the preadult populations of two medieval skeletal assemblages from Denmark. One is from a leprosarium, and thus probably represents a disadvantaged group (Naestved). The other comes from a normal, and in comparison rather privileged, medieval community (AEbelholt). Previous studies of the adult population indicated differences between the two skeletal collections with regard to mortality, dental size, and metabolic and specific infectious disease. The two samples were analyzed against the view known as the "osteological paradox" (Wood et al. [1992] Curr. Anthropol. 33:343-370), according to which skeletons displaying pathological modification are likely to represent the healthier individuals of a population, whereas those without lesions would have died without acquiring modifications as a result of a depressed immune response. Results reveal that older age groups among the preadults from Naestved are shorter and have less bone mineral content than their peers from AEbelholt. On average, the Naestved children have a higher prevalence of stress indicators, and in some cases display skeletal signs of leprosy. This is likely a result of the combination of compromised health and social disadvantage, thus supporting a more traditional interpretation. The study provides insights into the health of children from two different biocultural settings of medieval Danish society and illustrates the importance of comparing samples of single age groups.

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Small mammals and stray cats were trapped in two areas of North Zealand, Denmark, and their blood cultured for hemotrophic bacteria. Bacterial isolates were recovered in pure culture and subjected to 16S rDNA gene sequencing. Bartonella species were isolated from five mammalian species: B. grahamii from Microtus agrestis (field vole) and Apodemus flavicollis (yellow-necked field mouse); B. taylorii from M. agrestis, A. flavicollis and A. sylvaticus (long-tailed field mouse); B. tribocorum from A. flavicollis; R vinsonii subsp. vinsonii from M. agrestis and A. sylvaticus; and B. birtlesii from Sorex vulgaris (common shrew). In addition, two variant types of B. henselae were identified: variant I was recovered from three specimens of A. sylvaticus, and B. henselae variant 11 from I I cats; in each case this was the only B. henselae variant found. No Bartonella species was isolated from Clethrionomys glareolus (bank vole) or Micromys minutus (harvest mouse). These results suggest that B. henselae occurs in two animal reservoirs in this region, one of variant I in A. sylvaticus, which may be transmitted between mice by the tick Ixodes ricinus, and another of variant 11 in cats, which may be transmitted by the cat flea (Ctenocephalides felis). To our knowledge, this is the first report of the occurrence of B. henselae and B. tribocorum in Apodemus mice.

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Iphiseiodes zuluagai Denmark & Muma é um importante predador de Brevipalpus phoenicis (Geijskes) em citros no Brasil. O emprego de Tyrophagus putrescentiae (Schrank) como fonte de alimento para I. zuluagai em criações de laboratório foi investigado a 25,5 ± 0,5ºC, 88 ± 7% UR e fotofase de 12h. Inicialmente os níveis de oviposição do predador alimentado com ovos, estágios pós-embrionários mortos ou estágios pós-embrionários vivos de T. putrescentiae foram avaliados durante 10 dias. A taxa diária de oviposição foi de 1,3 ovo/ fêmea quando estas foram alimentadas com ovos de T. putrecentiae; 0,7 ovo/ fêmea quando estas foram alimentadas com estágios pós-embrionários mortos e cerca de 0,2 ovo/ fêmea quando alimentadas com estágios pós-embrionários vivos. Posteriormente, elaborou-se a tabela de vida de I. zuluagai, oferecendo-se como alimento ovos de T. putrescentiae. Os estágios imaturos foram observados a cada 8h, para determinar a duração correspondente. Na fase adulta, os ácaros foram observados a cada 24h, para se determinar os parâmetros reprodutivos. A capacidade de aumento populacional (r m) foi de 0,11 fêmea/ fêmea/ dia; resultando em uma razão finita de aumento de 1,11 (l). A taxa líquida de reprodução (R0) foi de 7,1 fêmeas/geração, com um tempo de geração de 18,6 dias. Os resultados obtidos mostram que T. putrescentiae é uma fonte de alimento favorável ao desenvolvimento de I. zuluagai.