7,282 research outputs found

    Exploiting the chaotic behaviour of atmospheric models with reconfigurable architectures

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    Reconfigurable architectures are becoming mainstream: Amazon, Microsoft and IBM are supporting such architectures in their data centres. The computationally intensive nature of atmospheric modelling is an attractive target for hardware acceleration using reconfigurable computing. Performance of hardware designs can be improved through the use of reduced-precision arithmetic, but maintaining appropriate accuracy is essential. We explore reduced-precision optimisation for simulating chaotic systems, targeting atmospheric modelling, in which even minor changes in arithmetic behaviour will cause simulations to diverge quickly. The possibility of equally valid simulations having differing outcomes means that standard techniques for comparing numerical accuracy are inappropriate. We use the Hellinger distance to compare statistical behaviour between reduced-precision CPU implementations to guide reconfigurable designs of a chaotic system, then analyse accuracy, performance and power efficiency of the resulting implementations. Our results show that with only a limited loss in accuracy corresponding to less than 10% uncertainty in input parameters, the throughput and energy efficiency of a single-precision chaotic system implemented on a Xilinx Virtex-6 SX475T Field Programmable Gate Array (FPGA) can be more than doubled

    Monoamine oxidase-A modulates apoptotic cell death induced by staurosporine in human neuroblastoma cells

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    Monoamine oxidases (MAOs) are mitochondrial enzymes which control the levels of neurotransmitters in the brain and dietary amines in peripheral tissues via oxidative deamination. MAO has also been implicated in cell signalling. In this study, we describe the MAO-A isoform as functional in apoptosis induced by staurosporine (STS) in human dopaminergic neuroblastoma cells (SH-SY5Y). Increased levels of MAO-A activity were induced by STS, accompanied by increased MAO-A protein and activation of the initiator of the intrinsic pathway, caspase 9, and the executioner caspase 3. MAO-A mRNA levels were unaffected by STS, suggesting that changes in MAO-A protein are due to post-transcriptional events. Two unrelated MAO-A inhibitors reduced caspase activation. STS treatment resulted in sustained activation of the mitogen-activated protein kinase pathway enzymes extracellular regulated kinase, c-jun terminal kinase and p38, and depletion of the anti-apoptotic protein Bcl-2. These changes were significantly reversed by MAO inhibition. Production of reactive oxygen species was increased following STS exposure, which was blocked by both MAO inhibition and the antioxidant N-acetylcysteine. Therefore our data provide evidence that MAO-A, through its production of reactive oxygen species as a by-product of its catalytic activity on the mitochondrial surface, is recruited by the cell to enhance apoptotic signalling

    Lower precision for higher accuracy: precision and resolution exploration for shallow water equations

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    Accurate forecasts of future climate with numerical models of atmosphere and ocean are of vital importance. However, forecast quality is often limited by the available computational power. This paper investigates the acceleration of a C-grid shallow water model through the use of reduced precision targeting FPGA technology. Using a double-gyre scenario, we show that the mantissa length of variables can be reduced to 14 bits without affecting the accuracy beyond the error inherent in the model. Our reduced precision FPGA implementation runs 5.4 times faster than a double precision FPGA implementation, and 12 times faster than a multi-Threaded CPU implementation. Moreover, our reduced precision FPGA implementation uses 39 times less energy than the CPU implementation and can compute a 100×100 grid for the same energy that the CPU implementation would take for a 29×29 grid

    Configuration Of Grafted Polystyrene Chains In The Melt: Temperature And Concentration Dependence

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    The concentration profiles of carboxy-terminated polystyrene chains in the melt grafted onto oxide-covered silicon substrates were measured using secondary-ion mass spectroscopy. The grafting density increased with temperature and an enthalpy of +7.4 kcal/mole was deduced for the grafting reaction, SiOH + R(COOH) ⇄ R(COOSi) + H2O. Relatively high grafting densities (σ∼6.6·mg/m2) were achieved with minimal chain distortion or displacement of long chains by shorter ones. Significant stretching of the grafted chains occurred for σ > 10 mg/m2. An equilibrium constant for the grafting reaction incorporating entropy is discussed.69577677

    Identification and Characterisation of the Early Differentiating Cells in Neural Differentiation of Human Embryonic Stem Cells

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    One of the challenges in studying early differentiation of human embryonic stem cells (hESCs) is being able to discriminate the initial differentiated cells from the original pluripotent stem cells and their committed progenies. It remains unclear how a pluripotent stem cell becomes a lineage-specific cell type during early development, and how, or if, pluripotent genes, such as Oct4 and Sox2, play a role in this transition. Here, by studying the dynamic changes in the expression of embryonic surface antigens, we identified the sequential loss of Tra-1-81 and SSEA4 during hESC neural differentiation and isolated a transient Tra-1-81(−)/SSEA4(+) (TR−/S4+) cell population in the early stage of neural differentiation. These cells are distinct from both undifferentiated hESCs and their committed neural progenitor cells (NPCs) in their gene expression profiles and response to extracellular signalling; they co-express both the pluripotent gene Oct4 and the neural marker Pax6. Furthermore, these TR−/S4+ cells are able to produce cells of both neural and non-neural lineages, depending on their environmental cues. Our results demonstrate that expression of the pluripotent factor Oct4 is progressively downregulated and is accompanied by the gradual upregulation of neural genes, whereas the pluripotent factor Sox2 is consistently expressed at high levels, indicating that these pluripotent factors may play different roles in the regulation of neural differentiation. The identification of TR-S4+ cells provides a cell model for further elucidation of the molecular mechanisms underlying hESC neural differentiation

    Experimental characterisation of dynamic properties of an all-FRP truss bridge

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    This is the author accepted manuscript. The final version is available from the publisher via the DOI in this recordFibre Reinforced Polymers (FRPs) have increasingly been utilised for construction of pedestrian bridges due to high strength- and stiffness-to-weight ratios, low maintenance costs and quick installation. Their relatively low mass and stiffness make these bridges potentially susceptible to vibration serviceability problems, which increasingly govern the design. Currently, the wider application of FRPs in civil engineering is hindered by the lack of experimental insight in dynamic performance of as-built structures. This paper presents an experimental investigation on a 25, m long glass-FRP truss footbridge in Italy. Ambient vibration tests were conducted to identify the dynamic properties. The peak-picking method and stochastic subspace identification approach were employed for modal parameter identification. The two methods produced very consistent results. Eight vibration modes were identified in the frequency range up to 10, Hz. Two lateral flexural vibration modes having natural frequencies of 5.8 and 9.6, Hz were identified, as well as two vertical flexural modes (at 7.5 and 8.1, Hz) and four torsional modes (at 2.1, 2.7, 4.8 and 9.3, Hz). Damping ratios for all modes up to 10, Hz except the eighth mode were above 1.2%.Engineering and Physical Sciences Research Council (EPSRC

    An integrated clinical-MR radiomics model to estimate survival time in patients with endometrial cancer

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    Background: Determination of survival time in women with endometrial cancer using clinical features remains imprecise. Features from MRI may improve the survival estimation allowing improved treatment planning. Purpose: To identify clinical features and imaging signatures on T2-weighted MRI that can be used in an integrated model to estimate survival time for endometrial cancer subjects. Study Type: Retrospective. Population: Four hundred thirteen patients with endometrial cancer as training (N = 330, 66.41 ± 11.42 years) and validation (N = 83, 67.60 ± 11.89 years) data and an independent set of 82 subjects as testing data (63.26 ± 12.38 years). Field Strength/Sequence: 1.5-T and 3-T scanners with sagittal T2-weighted spin echo sequence. Assessment: Tumor regions were manually segmented on T2-weighted images. Features were extracted from segmented masks, and clinical variables including age, cancer histologic grade and risk score were included in a Cox proportional hazards (CPH) model. A group least absolute shrinkage and selection operator method was implemented to determine the model from the training and validation datasets. Statistical Tests: A likelihood-ratio test and decision curve analysis were applied to compare the models. Concordance index (CI) and area under the receiver operating characteristic curves (AUCs) were calculated to assess the model. Results: Three radiomic features (two image intensity and volume features) and two clinical variables (age and cancer grade) were selected as predictors in the integrated model. The CI was 0.797 for the clinical model (includes clinical variables only) and 0.818 for the integrated model using training and validation datasets, the associated mean AUC value was 0.805 and 0.853. Using the testing dataset, the CI was 0.792 and 0.882, significantly different and the mean AUC was 0.624 and 0.727 for the clinical model and integrated model, respectively. Data Conclusion: The proposed CPH model with radiomic signatures may serve as a tool to improve estimated survival time in women with endometrial cancer

    Microscopic Theory of Heterogeneity and Non-Exponential Relaxations in Supercooled Liquids

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    Recent experiments and computer simulations show that supercooled liquids around the glass transition temperature are "dynamically heterogeneous" [1]. Such heterogeneity is expected from the random first order transition theory of the glass transition. Using a microscopic approach based on this theory, we derive a relation between the departure from Debye relaxation as characterized by the β\beta value of a stretched exponential response function ϕ(t)=e(t/τKWW)β\phi(t) =e^{-(t/ \tau_{KWW})^{\beta}}, and the fragility of the liquid. The β\beta value is also predicted to depend on temperature and to vanish as the ideal glass transition is approached at the Kauzmann temperature.Comment: 4 pages including 3 eps figure

    The Buckling Spectra of Nanoparticle Surfactant Assemblies

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    Fine control over the mechanical properties of thin sheets underpins transcytosis, cell shape, and morphogenesis. Applying these principles to artificial, liquid-based systems has led to reconfigurable materials for soft robotics, actuation, and chemical synthesis. However, progress is limited by a lack of synthetic two-dimensional membranes that exhibit tunable mechanical properties over a comparable range to that seen in nature. Here, we show that the bending modulus, B, of thin assemblies of nanoparticle surfactants (NPSs) at the oil–water interface can be varied continuously from sub-kBT to 106kBT, by varying the ligands and particles that comprise the NPS. We find extensive departure from continuum behavior, including enormous mechanical anisotropy and a power law relation between B and the buckling spectrum width. Our findings provide a platform for shape-changing liquid devices and motivate new theories for the description of thin-film wrinkling
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