140 research outputs found

    Dimensional Consistency Analysis in Complex Algebraic Models

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    Relations in complex algebraic models include numerous variables and parameter that capture the physical dimensions of the objects represented in models (such as "mass", or "volume" of an object). A model developer must ensure the semantic correctness of the model, which includes consistency across physical dimensions and their units of measure in the model relations. Such dimensional consistency analysis is the subject of the research described in this paper. We propose a new methodological framework for this type of analysis which comprises: - a two-level structure for representing knowledge about physical dimensions and units of measure; and - the dimensional analysis algorithm that uses this structured knowledge for the verification of consistency. The proposed methodology allows us to resolve issues related to handling complex non-decomposable units of measure and the situation when instances of the same physical dimension are associated with different physical quantities. We illustrate the proposed methodological framework using mathematical relations from a comprehensive environmental model developed at IIASA

    Naturalistic stimuli reveal a dominant role for agentic action in visual representation

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    Abstract Naturalistic, dynamic movies evoke strong, consistent, and information-rich patterns of activity over a broad expanse of cortex and engage multiple perceptual and cognitive systems in parallel. The use of naturalistic stimuli enables functional brain imaging research to explore cognitive domains that are poorly sampled in highly-controlled experiments. These domains include perception and understanding of agentic action, which plays a larger role in visual representation than was appreciated from experiments using static, controlled stimuli

    Neural Responses to Naturalistic Clips of Behaving Animals Under Two Different Task Contexts

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    The human brain rapidly deploys semantic information during perception to facilitate our interaction with the world. These semantic representations are encoded in the activity of distributed populations of neurons (Haxby et al., 2001; McClelland and Rogers, 2003; Kriegeskorte et al., 2008b) and command widespread cortical real estate (Binder et al., 2009; Huth et al., 2012). The neural representation of a stimulus can be described as a location (i.e., response vector) in a high-dimensional neural representational space (Kriegeskorte and Kievit, 2013; Haxby et al., 2014). This resonates with behavioral and theoretical work describing mental representations of objects and actions as being organized in a multidimensional psychological space (Attneave, 1950; Shepard, 1958, 1987; Edelman, 1998; Gärdenfors and Warglien, 2012). Current applications of this framework to neural representation (e.g., Kriegeskorte et al., 2008b) often implicitly assume that these neural representational spaces are relatively fixed and context-invariant. In contrast, earlier work emphasized the importance of attention and task demands in actively reshaping representational space (Shepard, 1964; Tversky, 1977; Nosofsky, 1986; Kruschke, 1992). A growing body of work in both electrophysiology (e.g., Sigala and Logothetis, 2002; Sigala, 2004; Cohen and Maunsell, 2009; Reynolds and Heeger, 2009) and human neuroimaging (e.g., Hon et al., 2009; Jehee et al., 2011; Brouwer and Heeger, 2013; Çukur et al., 2013; Sprague and Serences, 2013; Harel et al., 2014; Erez and Duncan, 2015; Nastase et al., 2017) has suggested mechanisms by which behavioral goals dynamically alter neural representation

    Modeling Semantic Encoding in a Common Neural Representational Space

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    Encoding models for mapping voxelwise semantic tuning are typically estimated separately for each individual, limiting their generalizability. In the current report, we develop a method for estimating semantic encoding models that generalize across individuals. Functional MRI was used to measure brain responses while participants freely viewed a naturalistic audiovisual movie. Word embeddings capturing agent-, action-, object-, and scene-related semantic content were assigned to each imaging volume based on an annotation of the film. We constructed both conventional within-subject semantic encoding models and between-subject models where the model was trained on a subset of participants and validated on a left-out participant. Between-subject models were trained using cortical surface-based anatomical normalization or surface-based whole-cortex hyperalignment. We used hyperalignment to project group data into an individual’s unique anatomical space via a common representational space, thus leveraging a larger volume of data for out-of-sample prediction while preserving the individual’s fine-grained functional–anatomical idiosyncrasies. Our findings demonstrate that anatomical normalization degrades the spatial specificity of between-subject encoding models relative to within-subject models. Hyperalignment, on the other hand, recovers the spatial specificity of semantic tuning lost during anatomical normalization, and yields model performance exceeding that of within-subject models

    Modeling Semantic Encoding in a Common Neural Representational Space

    Get PDF
    Encoding models for mapping voxelwise semantic tuning are typically estimated separately for each individual, limiting their generalizability. In the current report, we develop a method for estimating semantic encoding models that generalize across individuals. Functional MRI was used to measure brain responses while participants freely viewed a naturalistic audiovisual movie. Word embeddings capturing agent-, action-, object-, and scene-related semantic content were assigned to each imaging volume based on an annotation of the film. We constructed both conventional within-subject semantic encoding models and between-subject models where the model was trained on a subset of participants and validated on a left-out participant. Between-subject models were trained using cortical surface-based anatomical normalization or surface-based whole-cortex hyperalignment. We used hyperalignment to project group data into an individual’s unique anatomical space via a common representational space, thus leveraging a larger volume of data for out-of-sample prediction while preserving the individual’s fine-grained functional–anatomical idiosyncrasies. Our findings demonstrate that anatomical normalization degrades the spatial specificity of between-subject encoding models relative to within-subject models. Hyperalignment, on the other hand, recovers the spatial specificity of semantic tuning lost during anatomical normalization, and yields model performance exceeding that of within-subject models

    Mode regularization of the susy sphaleron and kink: zero modes and discrete gauge symmetry

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    To obtain the one-loop corrections to the mass of a kink by mode regularization, one may take one-half the result for the mass of a widely separated kink-antikink (or sphaleron) system, where the two bosonic zero modes count as two degrees of freedom, but the two fermionic zero modes as only one degree of freedom in the sums over modes. For a single kink, there is one bosonic zero mode degree of freedom, but it is necessary to average over four sets of fermionic boundary conditions in order (i) to preserve the fermionic Z2_2 gauge invariance ψψ\psi \to -\psi, (ii) to satisfy the basic principle of mode regularization that the boundary conditions in the trivial and the kink sector should be the same, (iii) in order that the energy stored at the boundaries cancels and (iv) to avoid obtaining a finite, uniformly distributed energy which would violate cluster decomposition. The average number of fermionic zero-energy degrees of freedom in the presence of the kink is then indeed 1/2. For boundary conditions leading to only one fermionic zero-energy solution, the Z2_2 gauge invariance identifies two seemingly distinct `vacua' as the same physical ground state, and the single fermionic zero-energy solution does not correspond to a degree of freedom. Other boundary conditions lead to two spatially separated ω0\omega \sim 0 solutions, corresponding to one (spatially delocalized) degree of freedom. This nonlocality is consistent with the principle of cluster decomposition for correlators of observables.Comment: 32 pages, 5 figure

    Strings in flat space and pp waves from N=4{\cal N}=4 Super Yang Mills

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    We explain how the string spectrum in flat space and pp-waves arises from the large NN limit, at fixed gYM2g^2_{YM}, of U(N) N=4{\cal N} =4 super Yang Mills. We reproduce the spectrum by summing a subset of the planar Feynman diagrams. We give a heuristic argument for why we can neglect other diagrams. We also discuss some other aspects of pp-waves and we present a matrix model associated to the DLCQ description of the maximally supersymmetric eleven dimensional pp-waves.Comment: 36 pages, 5 figures. v3: minor typos corrected, references adde

    Further properties of causal relationship: causal structure stability, new criteria for isocausality and counterexamples

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    Recently ({\em Class. Quant. Grav.} {\bf 20} 625-664) the concept of {\em causal mapping} between spacetimes --essentially equivalent in this context to the {\em chronological map} one in abstract chronological spaces--, and the related notion of {\em causal structure}, have been introduced as new tools to study causality in Lorentzian geometry. In the present paper, these tools are further developed in several directions such as: (i) causal mappings --and, thus, abstract chronological ones-- do not preserve two levels of the standard hierarchy of causality conditions (however, they preserve the remaining levels as shown in the above reference), (ii) even though global hyperbolicity is a stable property (in the set of all time-oriented Lorentzian metrics on a fixed manifold), the causal structure of a globally hyperbolic spacetime can be unstable against perturbations; in fact, we show that the causal structures of Minkowski and Einstein static spacetimes remain stable, whereas that of de Sitter becomes unstable, (iii) general criteria allow us to discriminate different causal structures in some general spacetimes (e.g. globally hyperbolic, stationary standard); in particular, there are infinitely many different globally hyperbolic causal structures (and thus, different conformal ones) on R2\R^2, (iv) plane waves with the same number of positive eigenvalues in the frequency matrix share the same causal structure and, thus, they have equal causal extensions and causal boundaries.Comment: 33 pages, 9 figures, final version (the paper title has been changed). To appear in Classical and Quantum Gravit

    Extensions, expansions, Lie algebra cohomology and enlarged superspaces

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    After briefly reviewing the methods that allow us to derive consistently new Lie (super)algebras from given ones, we consider enlarged superspaces and superalgebras, their relevance and some possible applications.Comment: 9 pages. Invited talk delivered at the EU RTN Workshop, Copenhagen, Sep. 15-19 and at the Argonne Workshop on Branes and Generalized Dynamics, Oct. 20-24, 2003. Only change: wrong number of a reference correcte
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