995 resultados para cable machinery


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Misiones, es una provincia pequeña, fronteriza y multicultural1, que se caracteriza por contar -a lo largo de su historia- con una variada y rica presencia de medios de comunicación. Desde el origen de los primeros parapetos (1872), pasando por los primeros diarios (1883), la aparición de la radio (1927) hasta llegar a la TV abierta (1972), existen una serie de emprendimientos comunicacionales llevados adelante con éxito por verdaderos pioneros en la materia. Es el caso de la televisión por cable, cuya existencia data desde 1964 en la ciudad de Posadas. Un medio pequeño que llegó a tener en su época de esplendor cerca de 4.000 usuarios. Esto nos permite pensar que más allá de los diversos contextos y momentos histórico, el ciudadano necesitó comunicar y comunicarse entre si y con los demás. El presente proyecto, es la continuidad de un trabajo de investigación que comenzó con la construcción de la historia de LT 85 TV Canal 12 de Posadas, que tiene por objetivo rescatar la memoria de los medios de comunicación de la Provincia de Misiones, en este caso, de Canal 2 de Posadas. Se intentará explorar los modos en que se creó, construyó y usó esta tecnología y los modos en que operó en prácticas y actos comunicativos de unos y otros, en espacios y tiempos múltiples.

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Misiones, es una provincia pequeña, fronteriza y multicultural que se caracteriza por contar -a lo largo de su historia- con una variada y rica presencia de medios de comunicación. Desde el origen de los primeros parapetos (1872), pasando por los primeros diarios (1883), la aparición de la radio (1927) hasta llegar a la TV abierta (1972), existen una serie de emprendimientos comunicacionales llevados adelante con éxito por verdaderos pioneros en la materia. Es el caso de la televisión por cable, cuya existencia data desde 1965 en la ciudad de Posadas. Un medio pequeño que llegó a tener en su época de esplendor cerca de 4.000 usuarios. Esto nos permite pensar que más allá de los diversos contextos y momentos históricos, el ciudadano necesitó comunicar y comunicarse entre sí y con los demás. El proyecto es la continuidad de un trabajo de investigación que comenzó con la construcción de la historia de LT 85 TV Canal 12 de Posadas y, tiene por objetivo rescatar la memoria de los medios de comunicación de la Provincia de Misiones, en este caso, Canal 2 de Posadas. Se intentará explorar los modos en que se creó, construyó y usó esta tecnología y los modos en que operó en prácticas y actos comunicativos de unos y otros, en espacios y tiempos múltiples.

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In the early part of 1899 the U.S.S. Nero was dispatched from San Francisco to survey a route for a telegraph cable between the United States, the Philippines Islands and Japan. Concurent with meteorological and oceanographic observations, closely spaced samples of bottom material were systematically sampled. They have been carefully accounted and described by James M. Flint in this volume. On the way, numerous submarine peaks were discovered. During this voyage U.S.S. Nero also took a sounding in the area of the Challenger Deep, recording a depth of 5269 fathoms (9636 m), the greatest depth recorded at that time. Carefull study of the deep-sea deposits have also revealed a number of manganese nodules and encrustations as well as micronodules.

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Under-deck cable-stayed bridges are very effective structural systems for which the strong contribution of the stay cables under live loading allows for the design of very slender decks for persistent and transient loading scenarios. Their behaviour when subjected to seismic excitation is investigated herein and a set of design criteria are presented that relate to the type and arrangement of bearings, the number and configuration of struts, and the transverse distribution of stay cables. The nonlinear behaviour of these bridges when subject to both near-field and far-field accelerograms has been thoroughly investigated through the use of incremental dynamic analyses. An intensity measure that reflects the pertinent contributions to response when several vibration modes are activated was proposed and is shown to be effective for the analysis of this structural type. The under-deck cable-stay system contributes in a very positive manner to reducing the response when the bridges are subject to very strong seismic excitation. For such scenarios, the reduction in the stiffness of the deck because of crack formation, when prestressed concrete decks are used, mobilises the cable system and enhances the overall performance of the system. Sets of natural accelerograms that are compliant with the prescriptions of Eurocode 8 were also applied to propose a set of design criteria for this bridge type in areas prone to earthquakes. Particular attention is given to outlining the optimal strategies for the deployment of bearings

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Cable-stayed bridges represent nowadays key points in transport networks and their seismic behavior needs to be fully understood, even beyond the elastic range of materials. Both nonlinear dynamic (NL-RHA) and static (pushover) procedures are currently available to face this challenge, each with intrinsic advantages and disadvantages, and their applicability in the study of the nonlinear seismic behavior of cable-stayed bridges is discussed here. The seismic response of a large number of finite element models with different span lengths, tower shapes and class of foundation soil is obtained with different procedures and compared. Several features of the original Modal Pushover Analysis (MPA) are modified in light of cable-stayed bridge characteristics, furthermore, an extension of MPA and a new coupled pushover analysis (CNSP) are suggested to estimate the complex inelastic response of such outstanding structures subjected to multi-axial strong ground motions.

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En el presente proyecto se realiza un estudio para la construcción de una cabecera de televisión por cable. Se trata de un proyecto puramente teórico en el que se especifican cada una de las partes que forman una cabecera de televisión y cómo funciona cada una de ellas. En un principio, se sitúa la cabecera de televisión dentro de una plataforma general de transmisión, para indicar sus funciones. Posteriormente, se analizan las distintas tecnologías que implementan esta transmisión y los estándares DVB que las rigen, como son DVB-C y DVB-C2 para las transmisiones por cable propiamente dichas y DVB-IPTV para las transmisiones por IP, para elegir cuál de las opciones es la más acertada y adaptar la cabecera de televisión a la misma. En cuanto al desarrollo teórico de la cabecera, se estudia el proceso que sigue la señal dentro de la misma, desde la recepción de los canales hasta el envío de los mismos hacia los hogares de los distintos usuarios, pasando previamente por las etapas de codificación y multiplexación. Además, se especifican los equipos necesarios para el correcto funcionamiento de cada una de las etapas. En la recepción, se reciben los canales por cada uno de los medios posibles (satélite, cable, TDT y estudio), que son demodulados y decodificados por el receptor. A continuación, son codificados (en este proyecto en MPEG-2 o H.264) para posteriormente ser multiplexados. En la etapa de multiplexación, se forma una trama Transport Stream por cada canal, compuesta por su flujo de video, audio y datos. Estos datos se trata de una serie de tablas (SI y PSI) que guían al set-topbox del usuario en la decodificación de los programas (tablas PSI) y que proporcionan información de cada uno de los mismos y del sistema (tablas SI). Con estas últimas el decodificador forma la EPG. Posteriormente, se realiza una segunda multiplexación, de forma que se incluyen múltiples programas en una sola trama Transport Stream (MPTS). Estos MPTS son los flujos que les son enviados a cada uno de los usuarios. El mecanismo de transmisión es de dos tipos en función del contenido y los destinatarios: multicast o unicast. Por último, se especifica el funcionamiento básico de un sistema de acceso condicional, así como su estructura, el cual es imprescindible en todas las cabeceras para asegurar que cada usuario solo visualiza los contenidos contratados. In this project, a study is realized for the cable television head-end construction . It is a theoretical project in which there are specified each of the parts that form a television headend and how their works each of them. At first, the television head-end places inside a general platform of transmission, to indicate its functions. Later, the different technologies that implement this transmission and the standards DVB that govern them are analyzed, since the standards that govern the cable transmissions (DVB-C and DVB-C2) to the standard that govern the IP transmissions (DVB-IPTV), to choose which of the options is the most guessed right and to adapt the television head-end to the same one. The theoretical development of the head-end, there is studied the process that follows the sign inside the same one, from the receipt of the channels up to the sending of the same ones towards the homes of the different users, happening before for the stages of codification and multiplexación. In addition, there are specified the equipments necessary for the correct functioning of each one of the stages. In the reception, the channels are receiving for each of the possible systems(satellite, cable, TDT and study), and they are demodulated and decoded by the receiver. Later, they are codified (in this project in MPEG-2 or H.264). The next stage is the stage of multiplexing. In the multiplexing stage, the channels are packetized in Transport Stream, composed by his video flow, audio and information. The information are composed by many tables(SI and PSI). The PSI tables guide the set-top-box of the user in the programs decoding and the SI tables provide information about the programs and system. With the information mentioned the decoder forms the EPG. Later, a second multiplexación is realized, so that there includes multiple programs in an alone Transport Stream (MPTS). These MPTS are the flows that are sent to each of the users. Two types of transmission are possible: unicast (VoD channels) and multicast (live channels). Finally, the basic functioning of a conditional access system is specified and his structure too, which is indispensable in all the head-end to assure that every users visualizes the contracted contents only.

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The writer would like to point out the existence of a very remarkable Spanish cable-stayed bridge built in 1925, wich is thus older than the first one recorded by the authors (and probably the pioneer in concrete-deck type). The Tempul Aqueduct was designed by the famous Professor Educardo Torroja. The deck is a concrete box girder sustained by two planes of 3 mm diam 37-wire double cables working at 27 kg/mm2.

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Some neural bruise prediction models have been implemented in the laboratory, for the most traded fruit species and varieties, allowing the prediction of the acceptability or rejectability for damages, with respect to the EC Standards. Different models have been built for both quasi-static (compression) and dynamic (impact) loads covering the whole commercial ripening period of fruits. A simulation process has been developed gathering the information on laboratory bruise models and load sensor calibrations for different electronic devices (IS-100 and DEA-1, for impact and compression loads respectively). Some evaluation methodology has been designed gathering the information on the mechanical properties of fruits and the loading records of electronic devices. The evaluation system allows to determine the current stage of fruit handling process and machinery.

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El presente proyecto tiene la finalidad de diseñar una herramienta mediante métodos numéricos implementados en Matlab que permita estudiar los fenómenos térmicos que tiene lugar en los cables subterráneos de potencia cuando se encuentran en carga. Y a partir de las soluciones obtenidas determinar la capacidad máxima del transporte del cable para un emplazamiento determinado.

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In hippocampal neurons, neurotransmitter release can be regulated by protein kinase A (PKA) through a direct action on the secretory machinery. To identify the site of PKA modulation, we have taken advantage of the ability of the neurotoxin Botulinum A to cleave the synaptic protein SNAP-25. Cleavage of this protein decreases the Ca2+ responsiveness of the secretory machinery by partially uncoupling Ca2+-sensing from fusion per se. This is expressed as a shift toward higher Ca2+ levels of the Ca2+ to neurotransmitter release relationship and as a perturbation of synaptic delay under conditions where secretion induced by the Ca2+-independent secretagogue ruthenium red is unimpaired. We find that SNAP-25 cleavage also perturbs PKA-dependent modulation of secretion; facilitation of ruthenium red-evoked neurotransmitter release by the adenylyl cyclase activator forskolin is blocked completely after Botulinum toxin A action. Together with our observation that forskolin modifies the Ca2+ to neurotransmitter release relationship, our results suggest that SNAP-25 acts as a functional linker between Ca2+ detection and fusion and that PKA modulates an early step in the secretory machinery related to calcium sensing to facilitate synaptic transmission.

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Rer1p, a Golgi membrane protein, is required for the correct localization of an endoplasmic reticulum (ER) membrane protein, Sec12p, by a retrieval mechanism from the cis-Golgi to the ER. To test whether or not the role of Rer1p is common to multiple ER membrane proteins, we examined the localization of two other ER membrane proteins, Sec71p and Sec63p, in the wild-type and rer1 mutant yeast cells, using their fusions with an α-mating factor precursor (Mfα1p). Although Sec71p and Sec63p have completely different topology from Sec12p, their Mfα1p fusion proteins were also mislocalized to the trans-Golgi in the rer1 mutant. Overexpression of these fusions caused their mislocalization to the trans-Golgi even in the wild-type cells, and this mislocalization was partially suppressed by the co-overexpression of Rer1p. Either Sec71p or an artificial chimeric protein whose ER localization depends on Rer1p gave a competitive effect on the localization of the Mfα1-Sec71p fusion, which was abolished in rer1. Thus, Rer1p appears to be one of the common limiting components in the retrieval machinery for ER membrane proteins. The results also suggest that Sec71p and Sec63p depend on ER-Golgi recycling, at least partly, for ER localization. We also examined the effect of a mutation in α-COP, a subunit of yeast coatomer, on the localization of these ER membrane proteins. The Mfα1p fusions of Sec12p, Sec71p, and Sec63p were all more or less mislocalized in ret1–1. These observations imply that the roles of Rer1p and coatomer are much more general than thought before.

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The MAL proteolipid is a nonglycosylated integral membrane protein found in glycolipid-enriched membrane microdomains. In polarized epithelial Madin-Darby canine kidney cells, MAL is necessary for normal apical transport and accurate sorting of the influenza virus hemagglutinin. MAL is thus part of the integral machinery for glycolipid-enriched membrane–mediated apical transport. At steady state, MAL is predominantly located in perinuclear vesicles that probably arise from the trans-Golgi network (TGN). To act on membrane traffic and to prevent their accumulation in the target compartment, integral membrane elements of the protein-sorting machinery should be itinerant proteins that cycle between the donor and target compartments. To establish whether MAL is an itinerant protein, we engineered the last extracellular loop of MAL by insertion of sequences containing the FLAG epitope or with sequences containing residues that became O-glycosylated within the cells or that displayed biotinylatable groups. The ectopic expression of these modified MAL proteins allowed us to investigate the surface expression of MAL and its movement through different compartments after internalization with the use of a combination of assays, including surface biotinylation, surface binding of anti-FLAG antibodies, neuraminidase sensitivity, and drug treatments. Immunofluorescence and flow cytometric analyses indicated that, in addition to its Golgi localization, MAL was also expressed on the cell surface, from which it was rapidly internalized. This retrieval implies transport through the endosomal pathway and requires endosomal acidification, because it can be inhibited by drugs such as chloroquine, monensin, and NH4Cl. Resialylation experiments of surface MAL treated with neuraminidase indicated that ∼30% of the internalized MAL molecules were delivered to the TGN, probably to start a new cycle of cargo transport. Together, these observations suggest that, as predicted for integral membrane members of the late protein transport machinery, MAL is an itinerant protein cycling between the TGN and the plasma membrane.

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We have examined the distribution of RNA transcription and processing factors in the amphibian oocyte nucleus or germinal vesicle. RNA polymerase I (pol I), pol II, and pol III occur in the Cajal bodies (coiled bodies) along with various components required for transcription and processing of the three classes of nuclear transcripts: mRNA, rRNA, and pol III transcripts. Among these components are transcription factor IIF (TFIIF), TFIIS, splicing factors, the U7 small nuclear ribonucleoprotein particle, the stem–loop binding protein, SR proteins, cleavage and polyadenylation factors, small nucleolar RNAs, nucleolar proteins that are probably involved in pre-rRNA processing, and TFIIIA. Earlier studies and data presented here show that several of these components are first targeted to Cajal bodies when injected into the oocyte and only subsequently appear in the chromosomes or nucleoli, where transcription itself occurs. We suggest that pol I, pol II, and pol III transcription and processing components are preassembled in Cajal bodies before transport to the chromosomes and nucleoli. Most components of the pol II transcription and processing pathway that occur in Cajal bodies are also found in the many hundreds of B-snurposomes in the germinal vesicle. Electron microscopic images show that B-snurposomes consist primarily, if not exclusively, of 20- to 30-nm particles, which closely resemble the interchromatin granules described from sections of somatic nuclei. We suggest the name pol II transcriptosome for these particles to emphasize their content of factors involved in synthesis and processing of mRNA transcripts. We present a model in which pol I, pol II, and pol III transcriptosomes are assembled in the Cajal bodies before export to the nucleolus (pol I), to the B-snurposomes and eventually to the chromosomes (pol II), and directly to the chromosomes (pol III). The key feature of this model is the preassembly of the transcription and processing machinery into unitary particles. An analogy can be made between ribosomes and transcriptosomes, ribosomes being unitary particles involved in translation and transcriptosomes being unitary particles for transcription and processing of RNA.

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Replication of the single-stranded linear DNA genome of parvovirus minute virus of mice (MVM) starts with complementary strand synthesis from the 3′-terminal snap-back telomere, which serves as a primer for the formation of double-stranded replicative form (RF) DNA. This DNA elongation reaction, designated conversion, is exclusively dependent on cellular factors. In cell extracts, we found that complementary strand synthesis was inhibited by the cyclin-dependent kinase inhibitor p21WAF1/CIP1 and rescued by the addition of proliferating cell nuclear antigen, arguing for the involvement of DNA polymerase (Pol) δ in the conversion reaction. In vivo time course analyses using synchronized MVM-infected A9 cells allowed initial detection of MVM RF DNA at the G1/S phase transition, coinciding with the onset of cyclin A expression and cyclin A-associated kinase activity. Under in vitro conditions, formation of RF DNA was efficiently supported by A9 S cell extracts, but only marginally by G1 cell extracts. Addition of recombinant cyclin A stimulated DNA conversion in G1 cell extracts, and correlated with a concomitant increase in cyclin A-associated kinase activity. Conversely, a specific antibody neutralizing cyclin A-dependent kinase activity, abolished the capacity of S cell extracts for DNA conversion. We found no evidence for the involvement of cyclin E in the regulation of the conversion reaction. We conclude that cyclin A is necessary for activation of complementary strand synthesis, which we propose as a model reaction to study the cell cycle regulation of the Pol δ-dependent elongation machinery.