4,384 research outputs found

    Effects of space flight factors on genetic diversity of Buchloe dactyloides seeds

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    The objective of this research was to investigate the effects of space flight factors on Buchloe dactyloides “Jingyin No.3” seeds. After the retrieval, basic turf characters of plants were tested. Among the 100 plants tested, 21 showed great change on phenotype characters, including leaf blade length and width, height, stem diameter, number of tillers, number and length of stolon, length of stolon inter node, leaf color and extent of leaf turning yellow. 33 primers were screened in inter-simple sequence repeats (ISSR) analysis to evaluate DNA variation between mutations and their ground controls. Results show that 15.6 reliable bands were generated by 7 primers, of which 12.9 (80.9%) were polymorphic. Based on the study, we can conclude that the space flight factors could induce inheritable mutagenic changes on B. dactyloides seeds, and do further research to demonstrate these changes in genetic material of the mutants.Key words: Genetic diversity, Buchloe dactyloides, spaceflight, inter-simple sequence repeats

    Phase diagram of Eu magnetic ordering in Sn-flux-grown Eu(Fe1x_{1-x}Cox_{x})2_{2}As2_{2} single crystals

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    The magnetic ground state of the Eu2+^{2+} moments in a series of Eu(Fe1x_{1-x}Cox_{x})2_{2}As2_{2} single crystals grown from the Sn flux has been investigated in detail by neutron diffraction measurements. Combined with the results from the macroscopic properties (resistivity, magnetic susceptibility and specific heat) measurements, a phase diagram describing how the Eu magnetic order evolves with Co doping in Eu(Fe1x_{1-x}Cox_{x})2_{2}As2_{2} is established. The ground-state magnetic structure of the Eu2+^{2+} spins is found to develop from the A-type antiferromagnetic (AFM) order in the parent compound, via the A-type canted AFM structure with some net ferromagnetic (FM) moment component along the crystallographic c\mathit{c} direction at intermediate Co doping levels, finally to the pure FM order at relatively high Co doping levels. The ordering temperature of Eu declines linearly at first, reaches the minimum value of 16.5(2) K around x\mathit{x} = 0.100(4), and then reverses upwards with further Co doping. The doping-induced modification of the indirect Ruderman-Kittel-Kasuya-Yosida (RKKY) interaction between the Eu2+^{2+} moments, which is mediated by the conduction d\mathit{d} electrons on the (Fe,Co)As layers, as well as the change of the strength of the direct interaction between the Eu2+^{2+} and Fe2+^{2+} moments, might be responsible for the change of the magnetic ground state and the ordering temperature of the Eu sublattice. In addition, for Eu(Fe1x_{1-x}Cox_{x})2_{2}As2_{2} single crystals with 0.10 \leqslant x\mathit{x} \leqslant 0.18, strong ferromagnetism from the Eu sublattice is well developed in the superconducting state, where a spontaneous vortex state is expected to account for the compromise between the two competing phenomena.Comment: 10 pages, 9 figure

    You can't see what you can't see: Experimental evidence for how much relevant information may be missed due to Google's Web search personalisation

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    The influence of Web search personalisation on professional knowledge work is an understudied area. Here we investigate how public sector officials self-assess their dependency on the Google Web search engine, whether they are aware of the potential impact of algorithmic biases on their ability to retrieve all relevant information, and how much relevant information may actually be missed due to Web search personalisation. We find that the majority of participants in our experimental study are neither aware that there is a potential problem nor do they have a strategy to mitigate the risk of missing relevant information when performing online searches. Most significantly, we provide empirical evidence that up to 20% of relevant information may be missed due to Web search personalisation. This work has significant implications for Web research by public sector professionals, who should be provided with training about the potential algorithmic biases that may affect their judgments and decision making, as well as clear guidelines how to minimise the risk of missing relevant information.Comment: paper submitted to the 11th Intl. Conf. on Social Informatics; revision corrects error in interpretation of parameter Psi/p in RBO resulting from discrepancy between the documentation of the implementation in R (https://rdrr.io/bioc/gespeR/man/rbo.html) and the original definition (https://dl.acm.org/citation.cfm?id=1852106) as per 20/05/201

    A new type of DC superconducting fault current limiter

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    Computing Platforms for Big Biological Data Analytics: Perspectives and Challenges.

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    The last decade has witnessed an explosion in the amount of available biological sequence data, due to the rapid progress of high-throughput sequencing projects. However, the biological data amount is becoming so great that traditional data analysis platforms and methods can no longer meet the need to rapidly perform data analysis tasks in life sciences. As a result, both biologists and computer scientists are facing the challenge of gaining a profound insight into the deepest biological functions from big biological data. This in turn requires massive computational resources. Therefore, high performance computing (HPC) platforms are highly needed as well as efficient and scalable algorithms that can take advantage of these platforms. In this paper, we survey the state-of-the-art HPC platforms for big biological data analytics. We first list the characteristics of big biological data and popular computing platforms. Then we provide a taxonomy of different biological data analysis applications and a survey of the way they have been mapped onto various computing platforms. After that, we present a case study to compare the efficiency of different computing platforms for handling the classical biological sequence alignment problem. At last we discuss the open issues in big biological data analytics

    A multiple exp-function method for nonlinear differential equations and its application

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    A multiple exp-function method to exact multiple wave solutions of nonlinear partial differential equations is proposed. The method is oriented towards ease of use and capability of computer algebra systems, and provides a direct and systematical solution procedure which generalizes Hirota's perturbation scheme. With help of Maple, an application of the approach to the 3+13+1 dimensional potential-Yu-Toda-Sasa-Fukuyama equation yields exact explicit 1-wave and 2-wave and 3-wave solutions, which include 1-soliton, 2-soliton and 3-soliton type solutions. Two cases with specific values of the involved parameters are plotted for each of 2-wave and 3-wave solutions.Comment: 12 pages, 16 figure

    Dual-responsive supramolecular colloidal microcapsules from cucurbit[8]uril molecular recognition in microfluidic droplets

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    The macrocyclic host, cucurbit[8]uril, is used to facilitate cross-linking of colloidal particles and polymers in microdroplets resulting in thermo- and photo-responsive supramolecular colloidal microcapsules. Methyl viologen-bearing colloidal particles were prepared using template polymerisation and combined with cucurbit[8]uril and an azobenzene-functionalised polymer within microfluidic droplets. The colloidal particles self-assembled at the droplet interface, whereupon polymeric cross-links formed via\textit{via} ternary host-guest complexation with cucurbit[8]uril. The resultant supramolecular colloidal microcapsules were uniform in size and were able to retain a macromolecular cargo. It is shown that the capsule skin porosity, and consequently the rate of release of encapsulated cargo, can be remotely controlled via\textit{via} either temperature or light triggers. This simple and versatile method could be extended to other polymer or colloidal derivatives for the fabrication of nano- and microcapsules with dual stimuli response for controlled release.Engineering and Physical Sciences Research Council (Grant IDs: EP/K503496/1, EP/H046593/1), CSC Cambridge Scholarshi
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