176,226 research outputs found

    Evidence for a quantum phase transition in electron-doped Pr2−x_{2-x}Cex_{x}CuO4−ή_{4-\delta} from Thermopower measurements

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    The evidence for a quantum phase transition under the superconducting dome in the high-TcT_c cuprates has been controversial. We report low temperature normal state thermopower(S) measurements in electron-doped Pr2−x_{2-x}Cex_{x}CuO4−ή_{4-\delta} as a function of doping (x from 0.11 to 0.19). We find that at 2K both S and S/T increase dramatically from x=0.11 to 0.16 and then saturate in the overdoped region. This behavior has a remarkable similarity to previous Hall effect results in Pr2−x_{2-x}Cex_{x}CuO4−ή_{4-\delta} . Our results are further evidence for an antiferromagnetic to paramagnetic quantum phase transition in electron-doped cuprates near x=0.16.Comment: 4 pages, 5 figure

    Intersections of homogeneous Cantor sets and beta-expansions

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    Let ΓÎČ,N\Gamma_{\beta,N} be the NN-part homogeneous Cantor set with ÎČ∈(1/(2N−1),1/N)\beta\in(1/(2N-1),1/N). Any string (jℓ)ℓ=1N(j_\ell)_{\ell=1}^\N with jℓ∈{0,±1,...,±(N−1)}j_\ell\in\{0,\pm 1,...,\pm(N-1)\} such that t=∑ℓ=1NjℓÎČℓ−1(1−ÎČ)/(N−1)t=\sum_{\ell=1}^\N j_\ell\beta^{\ell-1}(1-\beta)/(N-1) is called a code of tt. Let UÎČ,±N\mathcal{U}_{\beta,\pm N} be the set of t∈[−1,1]t\in[-1,1] having a unique code, and let SÎČ,±N\mathcal{S}_{\beta,\pm N} be the set of t∈UÎČ,±Nt\in\mathcal{U}_{\beta,\pm N} which make the intersection ΓÎČ,N∩(ΓÎČ,N+t)\Gamma_{\beta,N}\cap(\Gamma_{\beta,N}+t) a self-similar set. We characterize the set UÎČ,±N\mathcal{U}_{\beta,\pm N} in a geometrical and algebraical way, and give a sufficient and necessary condition for t∈SÎČ,±Nt\in\mathcal{S}_{\beta,\pm N}. Using techniques from beta-expansions, we show that there is a critical point ÎČc∈(1/(2N−1),1/N)\beta_c\in(1/(2N-1),1/N), which is a transcendental number, such that UÎČ,±N\mathcal{U}_{\beta,\pm N} has positive Hausdorff dimension if ÎČ∈(1/(2N−1),ÎČc)\beta\in(1/(2N-1),\beta_c), and contains countably infinite many elements if ÎČ∈(ÎČc,1/N)\beta\in(\beta_c,1/N). Moreover, there exists a second critical point αc=[N+1−(N−1)(N+3) ]/2∈(1/(2N−1),ÎČc)\alpha_c=\big[N+1-\sqrt{(N-1)(N+3)}\,\big]/2\in(1/(2N-1),\beta_c) such that SÎČ,±N\mathcal{S}_{\beta,\pm N} has positive Hausdorff dimension if ÎČ∈(1/(2N−1),αc)\beta\in(1/(2N-1),\alpha_c), and contains countably infinite many elements if ÎČ∈[αc,1/N)\beta\in[\alpha_c,1/N).Comment: 23 pages, 4 figure

    Classification of journal surfaces using surface topography parameters and software methods to compensate for stylus geometry

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    Measurements made with a stylus surface tracer which provides a digitized representation of a surface profile are discussed. Parameters are defined to characterize the height (e.g., RMS roughness, skewness, and kurtosis) and length (e.g., autocorrelation) of the surface topography. These are applied to the characterization of crank shaft journals which were manufactured by different grinding and lopping procedures known to give significant differences in crank shaft bearing life. It was found that three parameters (RMS roughness, skewness, and kurtosis) are necessary to adequately distinguish the character of these surfaces. Every surface specimen has a set of values for these three parameters. They can be regarded as a set coordinate in a space constituted by three characteristics axes. The various journal surfaces can be classified along with the determination of a proper wavelength cutoff (0.25 mm) by using a method of separated subspace. The finite radius of the stylus used for profile tracing gives an inherent measurement error as it passes over the fine structure of the surface. A mathematical model is derived to compensate for this error

    Simplifying the mosaic description of DNA sequences

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    By using the Jensen-Shannon divergence, genomic DNA can be divided into compositionally distinct domains through a standard recursive segmentation procedure. Each domain, while significantly different from its neighbours, may however share compositional similarity with one or more distant (non--neighbouring) domains. We thus obtain a coarse--grained description of the given DNA string in terms of a smaller set of distinct domain labels. This yields a minimal domain description of a given DNA sequence, significantly reducing its organizational complexity. This procedure gives a new means of evaluating genomic complexity as one examines organisms ranging from bacteria to human. The mosaic organization of DNA sequences could have originated from the insertion of fragments of one genome (the parasite) inside another (the host), and we present numerical experiments that are suggestive of this scenario.Comment: 16 pages, 1 figure, Accepted for publication in Phys. Rev.

    Distributed Adaptive Attitude Synchronization of Multiple Spacecraft

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    This paper addresses the distributed attitude synchronization problem of multiple spacecraft with unknown inertia matrices. Two distributed adaptive controllers are proposed for the cases with and without a virtual leader to which a time-varying reference attitude is assigned. The first controller achieves attitude synchronization for a group of spacecraft with a leaderless communication topology having a directed spanning tree. The second controller guarantees that all spacecraft track the reference attitude if the virtual leader has a directed path to all other spacecraft. Simulation examples are presented to illustrate the effectiveness of the results.Comment: 13 pages, 11 figures. To appear in SCIENCE CHINA Technological Science

    A cusp electron gun for millimeter wave gyrodevices

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    The experimental results of a thermionic cusp electron gun, to drive millimeter and submillimeter wave harmonic gyrodevices, are reported in this paper. Using a "smooth" magnetic field reversal formed by two coils this gun generated an annular-shaped, axis-encircling electron beam with 1.5 A current, and an adjustable velocity ratio alpha of up to 1.56 at a beam voltage of 40 kV. The beam cross-sectional shape and transported beam current were measured by a witness plate technique and Faraday cup, respectively. These measured results were found to be in excellent agreement with the simulated results using the three-dimensional code MAGIC

    New stopping criteria for segmenting DNA sequences

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    We propose a solution on the stopping criterion in segmenting inhomogeneous DNA sequences with complex statistical patterns. This new stopping criterion is based on Bayesian Information Criterion (BIC) in the model selection framework. When this stopping criterion is applied to a left telomere sequence of yeast Saccharomyces cerevisiae and the complete genome sequence of bacterium Escherichia coli, borders of biologically meaningful units were identified (e.g. subtelomeric units, replication origin, and replication terminus), and a more reasonable number of domains was obtained. We also introduce a measure called segmentation strength which can be used to control the delineation of large domains. The relationship between the average domain size and the threshold of segmentation strength is determined for several genome sequences.Comment: 4 pages, 4 figures, Physical Review Letters, to appea

    Exact scaling in the expansion-modification system

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    This work is devoted to the study of the scaling, and the consequent power-law behavior, of the correlation function in a mutation-replication model known as the expansion-modification system. The latter is a biology inspired random substitution model for the genome evolution, which is defined on a binary alphabet and depends on a parameter interpreted as a \emph{mutation probability}. We prove that the time-evolution of this system is such that any initial measure converges towards a unique stationary one exhibiting decay of correlations not slower than a power-law. We then prove, for a significant range of mutation probabilities, that the decay of correlations indeed follows a power-law with scaling exponent smoothly depending on the mutation probability. Finally we put forward an argument which allows us to give a closed expression for the corresponding scaling exponent for all the values of the mutation probability. Such a scaling exponent turns out to be a piecewise smooth function of the parameter.Comment: 22 pages, 2 figure

    Picoheterotroph (Bacteria and Archaea) biomass distribution in the global ocean

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    We compiled a database of 39 766 data points consisting of flow cytometric and microscopical measurements of picoheterotroph abundance, including both Bacteria and Archaea. After gridding with 1° spacing, the database covers 1.3% of the ocean surface. There are data covering all ocean basins and depths except the Southern Hemisphere below 350m or from April until June. The average picoheterotroph biomass is 3.9 ± 3.6 ”g Cl-1 with a 20-fold decrease between the surface and the deep sea. We estimate a total ocean inventory of about 1.3 × 1029 picoheterotroph cells. Surprisingly, the abundance in the coastal regions is the same as at the same depths in the open ocean. Using an average of published open ocean measurements for the conversion from abundance to carbon biomass of 9.1 fg cell-1, we calculate a picoheterotroph carbon inventory of about 1.2 Pg C. The main source of uncertainty in this inventory is the conversion factor from abundance to biomass. Picoheterotroph biomass is ? 2 times higher in the tropics than in the polar oceans
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