417 research outputs found
The fourth air quality daughter directive: Impacts and consequences of mandatory limit values
Jet pumps for thermoacoustic applications: design guidelines based on a numerical parameter study
The oscillatory flow through tapered cylindrical tube sections (jet pumps) is
characterized by a numerical parameter study. The shape of a jet pump results
in asymmetric hydrodynamic end effects which cause a time-averaged pressure
drop to occur under oscillatory flow conditions. Hence, jet pumps are used as
streaming suppressors in closed-loop thermoacoustic devices. A two-dimensional
axisymmetric computational fluid dynamics model is used to calculate the
performance of a large number of conical jet pump geometries in terms of
time-averaged pressure drop and acoustic power dissipation. The investigated
geometrical parameters include the jet pump length, taper angle, waist diameter
and waist curvature. In correspondence with previous work, four flow regimes
are observed which characterize the jet pump performance and dimensionless
parameters are introduced to scale the performance of the various jet pump
geometries. The simulation results are compared to an existing quasi-steady
theory and it is shown that this theory is only applicable in a small operation
region. Based on the scaling parameters, an optimum operation region is defined
and design guidelines are proposed which can be directly used for future jet
pump design.Comment: The following article has been accepted by the Journal of the
Acoustical Society of America. After it is published, it will be found at
http://scitation.aip.org/JAS
A numerical investigation on the vortex formation and flow separation of the oscillatory flow in jet pumps
A two-dimensional computational fluid dynamics model is used to predict the
oscillatory flow through a tapered cylindrical tube section (jet pump) placed
in a larger outer tube. Due to the shape of the jet pump, there will exist an
asymmetry in the hydrodynamic end effects which will cause a time-averaged
pressure drop to occur that can be used to cancel Gedeon streaming in a
closed-loop thermoacoustic device. The performance of two jet pump geometries
with different taper angles is investigated. A specific time-domain impedance
boundary condition is implemented in order to simulate traveling acoustic wave
conditions. It is shown that by scaling the acoustic displacement amplitude to
the jet pump dimensions, similar minor losses are observed independent of the
jet pump geometry. Four different flow regimes are distinguished and the
observed flow phenomena are related to the jet pump performance. The simulated
jet pump performance is compared to an existing quasi-steady approximation
which is shown to only be valid for small displacement amplitudes compared to
the jet pump length.Comment: The following article has been accepted by the Journal of the
Acoustical Society of America. After it is published, it will be found at:
http://scitation.aip.org/JAS
AFTER THE PARADIGM OF CONTEMPORARY PHYSICS IN ARCHITECTURE: SPATIAL POSSIBILITIES AND VARIATIONS
Living in the age of scientific, technological and digital revolution changes our attitude towards information. It is inevitable to start approaching information not only as a product of fashionable digital media behavior, but also as a particular accumulation of facts and activities, transferable bits of matter, which influence our environment. Architecture not only exerts spatial influence on our environment, but also it structures its processes. Acting as such, architecture is involved into direct representation of informational flows via organizing spatial systems. Therefore, in the digital era, design gets more related to transforming different informational modes into spatial structures. Transformations of information provide rich possibilities for conceptualizing space; such transformations could be achieved by different methodologies. This paper uses the concept of space in contemporary physics, namely the self-organizational behavior of the spacetime framework, in order to explore various ways of coding information in design. Analyzing String theory and its follower M – theory, the research derives a method for spatial organization of cause-and-effect activities resulting in a unified approach towards design methodology. This paper explores the concept of movement in the space-time framework, namely the movement in various dimensions and in non-Euclidean geometry, in order to develop a system for achieving a particular design control over informational activities. Using the topology of spacetime in String heory and M-theory, a topology produced as an outcome from that particular movement behavior, the research proposes a way to handle an informational status in the environment spatially. Such a design approach, becoming more and more necessary in the age of the digital, opens room not only for mere spatial variations, but also for a direction towards new design morphology; a morphology in which architecture obtains new spatial value, reaching beyond the label of visionary desig
Peribiliary glands are key in regeneration of the biliary epithelium after severe ischemic bile duct injury during liver transplantation
The systematic guideline review: method, rationale, and test on chronic heart failure
Background: Evidence-based guidelines have the potential to improve healthcare. However, their de-novo-development requires substantial resources-especially for complex conditions, and adaptation may be biased by contextually influenced recommendations in source guidelines. In this paper we describe a new approach to guideline development-the systematic guideline review method (SGR), and its application in the development of an evidence-based guideline for family physicians on chronic heart failure (CHF).
Methods: A systematic search for guidelines was carried out. Evidence-based guidelines on CHF management in adults in ambulatory care published in English or German between the years 2000 and 2004 were included. Guidelines on acute or right heart failure were excluded. Eligibility was assessed by two reviewers, methodological quality of selected guidelines was appraised using the AGREE instrument, and a framework of relevant clinical questions for diagnostics and treatment was derived. Data were extracted into evidence tables, systematically compared by means of a consistency analysis and synthesized in a preliminary draft. Most relevant primary sources were re-assessed to verify the cited evidence. Evidence and recommendations were summarized in a draft guideline.
Results: Of 16 included guidelines five were of good quality. A total of 35 recommendations were systematically compared: 25/35 were consistent, 9/35 inconsistent, and 1/35 un-rateable (derived from a single guideline). Of the 25 consistencies, 14 were based on consensus, seven on evidence and four differed in grading. Major inconsistencies were found in 3/9 of the inconsistent recommendations. We re-evaluated the evidence for 17 recommendations (evidence-based, differing evidence levels and minor inconsistencies) - the majority was congruent. Incongruity was found where the stated evidence could not be verified in the cited primary sources, or where the evaluation in the source guidelines focused on treatment benefits and underestimated the risks. The draft guideline was completed in 8.5 man-months. The main limitation to this study was the lack of a second reviewer.
Conclusion: The systematic guideline review including framework development, consistency analysis and validation is an effective, valid, and resource saving-approach to the development of evidence-based guidelines
Germ cell sex determination in mammals
One of the major decisions that germ cells make during their development is whether to differentiate into oocytes or sperm. In mice, the germ cells’ decision to develop as male or female depends on sex-determining signalling molecules in the embryonic gonadal environment rather than the sex chromosome constitution of the germ cells themselves. In response to these sex-determining cues, germ cells in female embryos initiate oogenesis and enter meiosis, whereas germ cells in male embryos initiate spermatogenesis and inhibit meiosis until after birth. However, it is not clear whether the signalling molecules that mediate germ cell sex determination act in the developing testis or the developing ovary, or what these signalling molecules might be. Here, we review the evidence for the existence of meiosis-inducing and meiosis-preventing substances in the developing gonad, and more recent studies aimed at identifying these molecules in mice. In addition, we discuss the possibility that some of the reported effects of these factors on germ cell development may be indirect consequences of impairing sexual differentiation of gonadal somatic cells or germ cell survival. Understanding the molecular mechanisms of germ cell sex determination may provide candidate genes for susceptibility to germ cell tumours and infertility in humans
Malignant germ cell tumours of childhood: new associations of genomic imbalance
Malignant germ cell tumours (MGCTs) of childhood are a rare group of neoplasms that comprise many histological subtypes and arise at numerous different sites. Genomic imbalances have been described in these tumours but, largely because of the paucity of cases reported in the literature, it is unclear how they relate to abnormalities in adult MGCTs and impact on potential systems for classifying GCTs. We have used metaphase-based comparative genomic hybridisation to analyse the largest series of paediatric MGCTs reported to date, representing 34 primary tumours (22 yolk sac tumours (YSTs), 11 germinomatous tumours and one metastatic embryonal carcinoma) occurring in children from birth to age 16, including 17 ovarian MGCTs. The large dataset enabled us to undertake statistical analysis, with the aim of identifying associations worthy of further investigation between patterns of genomic imbalance and clinicopathological parameters. The YSTs showed an increased frequency of 1p- (P=0.003), 3p+ (P=0.02), 4q− (P=0.07) and 6q− (P=0.004) compared to germinomatous tumours. Gain of 12p, which is invariably seen in adult MGCTs, was present in 53% of primary MGCTs of children aged 5–16 and was also observed in four of 14 YSTs affecting children less than 5. Two of these cases (14% of MGCTs in children less than 5) showed gain of the 12p11 locus considered to be particularly relevant in adult MGCTs. Gain of 12p showed a significant association with gain of 12q. Conversely, MGCTs without 12p gain displayed a significantly increased frequency of loss on 16p (P=0.04), suggesting that this imbalance may contribute to tumour development in such cases. This data provides new insight into the biology of this under-investigated tumour group and will direct future studies on the significance of specific genetic abnormalities
An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics
For a decade, The Cancer Genome Atlas (TCGA) program collected clinicopathologic annotation data along with multi-platform molecular profiles of more than 11,000 human tumors across 33 different cancer types. TCGA clinical data contain key features representing the democratized nature of the data collection process. To ensure proper use of this large clinical dataset associated with genomic features, we developed a standardized dataset named the TCGA Pan-Cancer Clinical Data Resource (TCGA-CDR), which includes four major clinical outcome endpoints. In addition to detailing major challenges and statistical limitations encountered during the effort of integrating the acquired clinical data, we present a summary that includes endpoint usage recommendations for each cancer type. These TCGA-CDR findings appear to be consistent with cancer genomics studies independent of the TCGA effort and provide opportunities for investigating cancer biology using clinical correlates at an unprecedented scale. Analysis of clinicopathologic annotations for over 11,000 cancer patients in the TCGA program leads to the generation of TCGA Clinical Data Resource, which provides recommendations of clinical outcome endpoint usage for 33 cancer types
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