87 research outputs found

    A counterexample to parabolic dichotomies in holomorphic iteration

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    We give an example of a parabolic holomorphic self-map ff of the unit ball B2C2\mathbb B^2\subset \mathbb C^2 whose canonical Kobayashi hyperbolic semi-model is given by an elliptic automorphism of the disc DC\mathbb D\subset \mathbb C, which can be chosen to be different from the identity. As a consequence, in contrast to the one dimensional case, this provides a first example of a holomorphic self-map of the unit ball which has points with zero hyperbolic step and points with nonzero hyperbolic step, solving an open question and showing that parabolic dynamics in the ball mathbbB2\\mathbb B^2 is radically different from parabolic dynamics in the disc. The example is obtained via a geometric method, embedding the ball B2\mathbb B^2 as a domain Ω\Omega in the bidisc mathbbD×H\\mathbb D\times \mathbb{H} that is forward invariant and absorbing for the map (z,w)(eiθz,w+1)(z,w)\mapsto (e^{i\theta}z,w+1), where HC\mathbb H\subset \mathbb C denotes the right half-plane. We also show that a complete Kobayashi hyperbolic domain Ω\Omega with such properties cannot be Gromov hyperbolic w.r.t. the Kobayashi distance (hence, it cannot be biholomorphic to mathbbB2\\mathbb B^2) if an additional quantitative geometric condition is satisfied

    Knowledge Graph Completion via Complex Tensor Factorization

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    In statistical relational learning, knowledge graph completion deals with automatically understanding the structure of large knowledge graphs—labeled directed graphs—and predicting missing relationships—labeled edges. State-of-the-art embedding models propose different trade-offs between modeling expressiveness, and time and space complexity. We reconcile both expressiveness and complexity through the use of complex-valued embeddings and explore the link between such complex-valued embeddings and unitary diagonalization. We corroborate our approach theoretically and show that all real square matrices—thus all possible relation/adjacency matrices—are the real part of some unitarily diagonalizable matrix. This results opens the door to a lot of other applications of square matrices factorization. Our approach based on complex embeddings is arguably simple, as it only involves a Hermitian dot product, the complex counterpart of the standard dot product between real vectors, whereas other methods resort to more and more complicated composition functions to increase their expressiveness. The proposed complex embeddings are scalable to large data sets as it remains linear in both space and time, while consistently outperforming alternative approaches on standard link prediction benchmarks

    French-English Terminology Extraction from Comparable Corpora

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    Evaluation of the Oscillatory Interference Model of Grid Cell Firing through Analysis and Measured Period Variance of Some Biological Oscillators

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    Models of the hexagonally arrayed spatial activity pattern of grid cell firing in the literature generally fall into two main categories: continuous attractor models or oscillatory interference models. Burak and Fiete (2009, PLoS Comput Biol) recently examined noise in two continuous attractor models, but did not consider oscillatory interference models in detail. Here we analyze an oscillatory interference model to examine the effects of noise on its stability and spatial firing properties. We show analytically that the square of the drift in encoded position due to noise is proportional to time and inversely proportional to the number of oscillators. We also show there is a relatively fixed breakdown point, independent of many parameters of the model, past which noise overwhelms the spatial signal. Based on this result, we show that a pair of oscillators are expected to maintain a stable grid for approximately t = 5µ3/(4πσ)2 seconds where µ is the mean period of an oscillator in seconds and σ2 its variance in seconds2. We apply this criterion to recordings of individual persistent spiking neurons in postsubiculum (dorsal presubiculum) and layers III and V of entorhinal cortex, to subthreshold membrane potential oscillation recordings in layer II stellate cells of medial entorhinal cortex and to values from the literature regarding medial septum theta bursting cells. All oscillators examined have expected stability times far below those seen in experimental recordings of grid cells, suggesting the examined biological oscillators are unfit as a substrate for current implementations of oscillatory interference models. However, oscillatory interference models can tolerate small amounts of noise, suggesting the utility of circuit level effects which might reduce oscillator variability. Further implications for grid cell models are discussed

    Odor supported place cell model and goal navigation in rodents

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    Experiments with rodents demonstrate that visual cues play an important role in the control of hippocampal place cells and spatial navigation. Nevertheless, rats may also rely on auditory, olfactory and somatosensory stimuli for orientation. It is also known that rats can track odors or self-generated scent marks to find a food source. Here we model odor supported place cells by using a simple feed-forward network and analyze the impact of olfactory cues on place cell formation and spatial navigation. The obtained place cells are used to solve a goal navigation task by a novel mechanism based on self-marking by odor patches combined with a Q-learning algorithm. We also analyze the impact of place cell remapping on goal directed behavior when switching between two environments. We emphasize the importance of olfactory cues in place cell formation and show that the utility of environmental and self-generated olfactory cues, together with a mixed navigation strategy, improves goal directed navigation

    Viral capsids: Mechanical characteristics, genome packaging and delivery mechanisms

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    The main functions of viral capsids are to protect, transport and deliver their genome. The mechanical properties of capsids are supposed to be adapted to these tasks. Bacteriophage capsids also need to withstand the high pressures the DNA is exerting onto it as a result of the DNA packaging and its consequent confinement within the capsid. It is proposed that this pressure helps driving the genome into the host, but other mechanisms also seem to play an important role in ejection. DNA packaging and ejection strategies are obviously dependent on the mechanical properties of the capsid. This review focuses on the mechanical properties of viral capsids in general and the elucidation of the biophysical aspects of genome packaging mechanisms and genome delivery processes of double-stranded DNA bacteriophages in particular
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