11,267 research outputs found

    How stationary are the internal tides in a high‐resolution global ocean circulation model?

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    The stationarity of the internal tides generated in a global eddy‐resolving ocean circulation model forced by realistic atmospheric fluxes and the luni‐solar gravitational potential is explored. The root mean square (RMS) variability in the M 2 internal tidal amplitude is approximately 2 mm or less over most of the ocean and exceeds 2 mm in regions with larger internal tidal amplitude. The M 2 RMS variability approaches the mean amplitude in weaker tidal areas such as the tropical Pacific and eastern Indian Ocean, but is smaller than the mean amplitude near generation regions. Approximately 60% of the variance in the complex M 2 tidal amplitude is due to amplitude‐weighted phase variations. Using the RMS tidal amplitude variations normalized by the mean tidal amplitude (normalized RMS variability (NRMS)) as a metric for stationarity, low‐mode M 2 internal tides with NRMS < 0.5 are stationary over 25% of the deep ocean, particularly near the generation regions. The M 2 RMS variability tends to increase with increasing mean amplitude. However, the M 2 NRMS variability tends to decrease with increasing mean amplitude, and regions with strong low‐mode internal tides are more stationary. The internal tide beams radiating away from generation regions become less stationary with distance. Similar results are obtained for other tidal constituents with the overall stationarity of the constituent decreasing as the energy in the constituent decreases. Seasonal variations dominate the RMS variability in the Arabian Sea and near‐equatorial oceans. Regions of high eddy kinetic energy are regions of higher internal tide nonstationarity. Key Points Internal tide stationarity measured by RMS variability normalized by amplitude Internal tide stationarity correlated with tidal amplitude Strong mesoscale eddies or currents decrease stationarity of internal tidesPeer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/107478/1/jgrc20664.pd

    Adaptive computation of multiscale entropy and its application in EEG signals for monitoring depth of anesthesia during surgery

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    Entropy as an estimate of complexity of the electroencephalogram is an effective parameter for monitoring the depth of anesthesia (DOA) during surgery. Multiscale entropy (MSE) is useful to evaluate the complexity of signals over different time scales. However, the limitation of the length of processed signal is a problem due to observing the variation of sample entropy (SE) on different scales. In this study, the adaptive resampling procedure is employed to replace the process of coarse-graining in MSE. According to the analysis of various signals and practical EEG signals, it is feasible to calculate the SE from the adaptive resampled signals, and it has the highly similar results with the original MSE at small scales. The distribution of the MSE of EEG during the whole surgery based on adaptive resampling process is able to show the detailed variation of SE in small scales and complexity of EEG, which could help anesthesiologists evaluate the status of patients.The Center for Dynamical Biomarkers and Translational Medicine, National Central University, Taiwan which is sponsored by National Science Council (Grant Number: NSC 100-2911-I-008-001). Also, it was supported by Chung-Shan Institute of Science & Technology in Taiwan (Grant Numbers: CSIST-095-V101 and CSIST-095-V102). Furthermore, it was supported by the National Science Foundation of China (No.50935005)

    Robust, reproducible, industrialized, standard membrane feeding assay for assessing the transmission blocking activity of vaccines and drugs against Plasmodium falciparum.

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    BackgroundA vaccine that interrupts malaria transmission (VIMT) would be a valuable tool for malaria control and elimination. One VIMT approach is to identify sexual erythrocytic and mosquito stage antigens of the malaria parasite that induce immune responses targeted at disrupting parasite development in the mosquito. The standard Plasmodium falciparum membrane-feeding assay (SMFA) is used to assess transmission-blocking activity (TBA) of antibodies against candidate immunogens and of drugs targeting the mosquito stages. To develop its P. falciparum sporozoite (SPZ) products, Sanaria has industrialized the production of P. falciparum-infected Anopheles stephensi mosquitoes, incorporating quantitative analyses of oocyst and P. falciparum SPZ infections as part of the manufacturing process.MethodsThese capabilities were exploited to develop a robust, reliable, consistent SMFA that was used to assess 188 serum samples from animals immunized with the candidate vaccine immunogen, Pfs25, targeting P. falciparum mosquito stages. Seventy-four independent SMFAs were performed. Infection intensity (number of oocysts/mosquito) and infection prevalence (percentage of mosquitoes infected with oocysts) were compared between mosquitoes fed cultured gametocytes plus normal human O(+) serum (negative control), anti-Pfs25 polyclonal antisera (MRA39 or MRA38, at a final dilution in the blood meal of 1:54 as positive control), and test sera from animals immunized with Pfs25 (at a final dilution in the blood meal of 1:9).ResultsSMFA negative controls consistently yielded high infection intensity (mean = 46.1 oocysts/midgut, range of positives 3.7-135.6) and infection prevalence (mean = 94.2%, range 71.4-100.0) and in positive controls, infection intensity was reduced by 81.6% (anti-Pfs25 MRA39) and 97.0% (anti-Pfs25 MRA38), and infection prevalence was reduced by 12.9 and 63.5%, respectively. A range of TBAs was detected among the 188 test samples assayed in duplicate. Consistent administration of infectious gametocytes to mosquitoes within and between assays was achieved, and the TBA of anti-Pfs25 control antibodies was highly reproducible.ConclusionsThese results demonstrate a robust capacity to perform the SMFA in a medium-to-high throughput format, suitable for assessing large numbers of experimental samples of candidate antibodies or drugs

    Collineation group as a subgroup of the symmetric group

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    Let Ψ\Psi be the projectivization (i.e., the set of one-dimensional vector subspaces) of a vector space of dimension ≥3\ge 3 over a field. Let HH be a closed (in the pointwise convergence topology) subgroup of the permutation group SΨ\mathfrak{S}_{\Psi} of the set Ψ\Psi. Suppose that HH contains the projective group and an arbitrary self-bijection of Ψ\Psi transforming a triple of collinear points to a non-collinear triple. It is well-known from \cite{KantorMcDonough} that if Ψ\Psi is finite then HH contains the alternating subgroup AΨ\mathfrak{A}_{\Psi} of SΨ\mathfrak{S}_{\Psi}. We show in Theorem \ref{density} below that H=SΨH=\mathfrak{S}_{\Psi}, if Ψ\Psi is infinite.Comment: 9 page

    Partiality, revisited: the partiality monad as a quotient inductive-inductive type

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    Capretta's delay monad can be used to model partial computations, but it has the "wrong" notion of built-in equality, strong bisimilarity. An alternative is to quotient the delay monad by the "right" notion of equality, weak bisimilarity. However, recent work by Chapman et al. suggests that it is impossible to define a monad structure on the resulting construction in common forms of type theory without assuming (instances of) the axiom of countable choice. Using an idea from homotopy type theory - a higher inductive-inductive type - we construct a partiality monad without relying on countable choice. We prove that, in the presence of countable choice, our partiality monad is equivalent to the delay monad quotiented by weak bisimilarity. Furthermore we outline several applications

    Scaling Behaviour and Complexity of the Portevin-Le Chatelier Effect

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    The plastic deformation of dilute alloys is often accompanied by plastic instabilities due to dynamic strain aging and dislocation interaction. The repeated breakaway of dislocations from and their recapture by solute atoms leads to stress serrations and localized strain in the strain controlled tensile tests, known as the Portevin-Le Chatelier (PLC) effect. In this present work, we analyse the stress time series data of the observed PLC effect in the constant strain rate tensile tests on Al-2.5%Mg alloy for a wide range of strain rates at room temperature. The scaling behaviour of the PLC effect was studied using two complementary scaling analysis methods: the finite variance scaling method and the diffusion entropy analysis. From these analyses we could establish that in the entire span of strain rates, PLC effect showed Levy walk property. Moreover, the multiscale entropy analysis is carried out on the stress time series data observed during the PLC effect to quantify the complexity of the distinct spatiotemporal dynamical regimes. It is shown that for the static type C band, the entropy is very low for all the scales compared to the hopping type B and the propagating type A bands. The results are interpreted considering the time and length scales relevant to the effect.Comment: 35 pages, 6 figure
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