899 resultados para Metafísica Grecia s.IV a.C.


Relevância:

30.00% 30.00%

Publicador:

Resumo:

Context. The first soft gamma-ray repeater was discovered over three decades ago, and was subsequently identified as a magnetar, a class of highly magnetised neutron star. It has been hypothesised that these stars power some of the brightest supernovae known, and that they may form the central engines of some long duration gamma-ray bursts. However there is currently no consenus on the formation channel(s) of these objects. Aims. The presence of a magnetar in the starburst cluster Westerlund 1 implies a progenitor with a mass ≥40 M⊙, which favours its formation in a binary that was disrupted at supernova. To test this hypothesis we conducted a search for the putative pre-SN companion. Methods. This was accomplished via a radial velocity survey to identify high-velocity runaways, with subsequent non-LTE model atmosphere analysis of the resultant candidate, Wd1-5. Results. Wd1-5 closely resembles the primaries in the short-period binaries, Wd1-13 and 44, suggesting a similar evolutionary history, although it currently appears single. It is overluminous for its spectroscopic mass and we find evidence of He- and N-enrichement, O-depletion, and critically C-enrichment, a combination of properties that is difficult to explain under single star evolutionary paradigms. We infer a pre-SN history for Wd1-5 which supposes an initial close binary comprising two stars of comparable (~ 41 M⊙ + 35 M⊙) masses. Efficient mass transfer from the initially more massive component leads to the mass-gainer evolving more rapidly, initiating luminous blue variable/common envelope evolution. Reverse, wind-driven mass transfer during its subsequent WC Wolf-Rayet phase leads to the carbon pollution of Wd1-5, before a type Ibc supernova disrupts the binary system. Under the assumption of a physical association between Wd1-5 and J1647-45, the secondary is identified as the magnetar progenitor; its common envelope evolutionary phase prevents spin-down of its core prior to SN and the seed magnetic field for the magnetar forms either in this phase or during the earlier episode of mass transfer in which it was spun-up. Conclusions. Our results suggest that binarity is a key ingredient in the formation of at least a subset of magnetars by preventing spin-down via core-coupling and potentially generating a seed magnetic field. The apparent formation of a magnetar in a Type Ibc supernova is consistent with recent suggestions that superluminous Type Ibc supernovae are powered by the rapid spin-down of these objects.

Relevância:

30.00% 30.00%

Publicador:

Resumo:

Esta investigación establece la secuencia estratigráfica, cronológica y funcional de un núcleo de poblamiento suburbano del municipio romano de Lucentum, con el fin de dibujar las líneas maestras de la evolución productiva de su ager periurbano. El yacimiento presenta cuatro fases principales que abarcan un dilatado arco temporal: estructuras de época tardorrepublicana (fase I, ss. II-I aC), una reestructuración viaria y urbanística de época augustea (fase II), el desarrollo de una villa con estructuras de transformación mercantil datada a partir de época tardojulia o flavia (fase III) y, por último, una fase bajoimperial (fase IV, ss. IV-v dC), en la que la villa sufre fuertes reestructuraciones.

Relevância:

30.00% 30.00%

Publicador:

Resumo:

Dada a importância que o Catálogo da Livraria de D. João IV, tem para o estudo da música ibérica, nos finais do séc. XVI e princípios do XVII, , e pelo facto de Manuel de Tavares ser o sexto compositor nele mais representado fez-se uma descrição da informação disponível sobre as suas composições constantes no catálogo, e a identificação hipotética daquelas que sobreviveram. Essa descrição constou dos seguintes parâmetros: número de vozes versando obras policorais e para um só coro; número de obras sacras em Latim e vilancicos; géneros músico-liturgicos, ocasião litúrgica para que foram escritas as composições, classificação dada pelo Rei (MB ou B) e línguas utilizadas nos vilancicos.

Relevância:

30.00% 30.00%

Publicador:

Resumo:

Long paper notebook with a handwritten inventory of Gannett's estate arranged by house location with price estimates. The inventory appears to correspond with the "Sales at auction" document. The verso of the last page contains the note: "Inventory of Personal Estate (copy)."

Relevância:

30.00% 30.00%

Publicador:

Resumo:

Handwritten list of five directives for completing the title search on a property purchased by a Mr. Harris from Andrew Bordman IV. The property was inherited from Bordman's mother Sarah, who in turn received the property from the estate of her brother Spencer Phips.

Relevância:

30.00% 30.00%

Publicador:

Resumo:

Introdution: Haemochromatosis-type IV, the ferroportin disease, is characterized by an autosomal-dominant transmission and early iron accumulation in macrophages. It is caused by mutations in the transmembrane iron exporter protein ferroportin1 (SLC40A1 gene). In form A (classic), ferroportin loss of function mutants are unable to export iron from cells leading to cellular iron accumulation with decreased availability of iron for serum transferrin (TS). We present a Portuguese rare clinical case of HH-IV. Materials and Methods: A 41-year-old woman with hyperferritinemia and normal TS. Causes of hyperferritinemia (inflammation, chronic alcohol consumption, metabolic syndrome, cell necrosis, non-alcoholic fatty liver disease and aceruloplasminemia) were assessed. Liver iron, evaluated by magnetic resonance imaging (MRI) was carried out. Screening for mutation in HFE and SCL40A1 genes were performed by Sanger sequencing. Baseline: Ferritin:708ng/ml; TS: 27%; MRI:85µmol/g; Hb:13,6g/dl. Therapy: weekly 450ml Therapeutic Phlebotomies (TP) until ferritin≤50ng/ml. Results: Hyperferritinemia comorbidities and common genetic mutations for haemochromatosis were negative. However, sequencing of the patient SLC40A1 gene has revealed the presence in heterozygosity of the variant c.238G>A; p.Gly80Ser. Due to low tolerance to TP, we adopted smaller phlebotomies every three weeks. Conclusion: This patient has a rare autosomal-dominant Ferroportin disease due to a mutated ferroportin which is predicted to be defective in iron cellular export. In agreement, she presents hyperferritinemia, with normal TS and liver iron overload. The genotype/phenotype association allowed to diagnosis this rare FD case. Although a mild form A, we decided to start TP. Her father also has been treated for iron overload.

Relevância:

30.00% 30.00%

Publicador:

Resumo:

From the above and the grafical results it can be concluded that cores in the research area are locally dominated by turbiditic sequences, which can be observed by a strong increase in coarser sediment (>35 µm). These coarser intercalations are lacking in the vicinity of basaltic seamounts, probably due to a shadowing effect of the seamounts. The infill of the King George Basin might be dominated by a north eastern current. Sedimentary structures as observed in the cores are often lacking or vague due to hydrothermal effects (Suess, L, 1986).

Relevância:

30.00% 30.00%

Publicador:

Resumo:

Transportation Department, Office of Noise Abatement, Washington, D.C.

Relevância:

30.00% 30.00%

Publicador:

Resumo:

National Highway Traffic Safety Administration, Washington, D.C.

Relevância:

30.00% 30.00%

Publicador:

Resumo:

National Highway Traffic Safety Administration, Washington, D.C.

Relevância:

30.00% 30.00%

Publicador:

Resumo:

National Highway Traffic Safety Administration, Office of Research and Development, Washington D.C.

Relevância:

30.00% 30.00%

Publicador:

Resumo:

Federal Highway Administration, Structures and Applied Mechanics Division, Washington, D.C.

Relevância:

30.00% 30.00%

Publicador:

Resumo:

Mode of access: Internet.