101 research outputs found
Les placements des organismes d’assurance à fin 2010.
L’analyse de la composition des portefeuilles des assureurs à fin 2010 révèle l’amorce d’un recentrage de leurs positions vers les titres émis par des signatures résidentes ainsi qu’un allongement de la durée moyenne de leurs placements obligataires.organismes d’assurance, assureurs vie, assureurs vie-mixte, assureurs non-vie, provisions techniques, contrats en euros, contrats en unités de compte, placements financiers, mise en transparence, épargne des ménages, circuits de financement, titres de créance, obligations, actions.
Turbulent thermal diffusion in a multi-fan turbulence generator with the imposed mean temperature gradient
We studied experimentally the effect of turbulent thermal diffusion in a
multi-fan turbulence generator which produces a nearly homogeneous and
isotropic flow with a small mean velocity. Using Particle Image Velocimetry and
Image Processing techniques we showed that in a turbulent flow with an imposed
mean vertical temperature gradient (stably stratified flow) particles
accumulate in the regions with the mean temperature minimum. These experiments
detected the effect of turbulent thermal diffusion in a multi-fan turbulence
generator for relatively high Reynolds numbers. The experimental results are in
compliance with the results of the previous experimental studies of turbulent
thermal diffusion in oscillating grids turbulence (Buchholz et al. 2004;
Eidelman et al. 2004). We demonstrated that turbulent thermal diffusion is an
universal phenomenon. It occurs independently of the method of turbulence
generation, and the qualitative behavior of particle spatial distribution in
these very different turbulent flows is similar. Competition between turbulent
fluxes caused by turbulent thermal diffusion and turbulent diffusion determines
the formation of particle inhomogeneities.Comment: 9 pages, 9 figure, REVTEX4, Experiments in Fluids, in pres
Разработка автоматизированного ИТП жилого здания
Объектом разработки системы является жилой дом с инженерными сетями в микрорайоне «Северный» в Заречном поселении Томского района Томской области.
Целью работы является разработка системы мониторинга и управления теплопотреблением здания, которая позволит вести точный учет потребляемой тепловой энергии, регулировать объем потребления в зависимости от текущих погодных условий, обеспечивать экономию энергоресурсов.
В результате разработана система, содержащая в себе компоненты, позволяющие производить учет и управление теплопотреблением здания. Причем все данные о работе системы, объемах потребления и параметрах теплоносителя поступают диспетчеру, имеющему возможность отслеживать все параметры системы удаленно.The object of the development of the system is a residential building with engineering services in the neighborhood "North" in Zarechny settlement Tomsk region Tomsk region.
The aim is to develop a building heat consumption monitoring and control system that will keep accurate records of heat energy consumption, adjusted consumption, depending on the current weather conditions, to ensure energy saving.
As a result, we developed a system, which contains the components to allow for registration and control of heat consumption of the building. Moreover, all data on the system performance, volume and consumption parameters receives coolant controller having the ability to track all system parameters remotely
Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease
<p>Abstract</p> <p>Background</p> <p>X-linked Charcot-Marie Tooth (CMT) is caused by mutations in the connexin32 gene that encodes a polypeptide which is arranged in hexameric array and form gap junctions.</p> <p>Methods</p> <p>We describe two novel mutations in the connexin32 gene in two Norwegian families.</p> <p>Results</p> <p>Family 1 had a c.225delG (R75fsX83) which causes a frameshift and premature stop codon at position 247. This probably results in a shorter non-functional protein structure. Affected individuals had an early age at onset usually in the first decade. The symptoms were more severe in men than women. All had severe muscle weakness in the legs. Several abortions were observed in this family. Family 2 had a c.536 G>A (C179Y) transition which causes a change of the highly conserved cysteine residue, i.e. disruption of at least one of three disulfide bridges. The mean age at onset was in the first decade. Muscle wasting was severe and correlated with muscle weakness in legs. The men and one woman also had symptom from their hands.</p> <p>The neuropathy is demyelinating and the nerve conduction velocities were in the intermediate range (25–49 m/s). Affected individuals had symmetrical clinical findings, while the neurophysiology revealed minor asymmetrical findings in nerve conduction velocity in 6 of 10 affected individuals.</p> <p>Conclusion</p> <p>The two novel mutations in the connexin32 gene are more severe than the majority of previously described mutations possibly due to the severe structural change of the gap junction they encode.</p
Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy
Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases
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