648 research outputs found

    Effectiveness of Hindman's theorem for bounded sums

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    We consider the strength and effective content of restricted versions of Hindman's Theorem in which the number of colors is specified and the length of the sums has a specified finite bound. Let HTkn\mathsf{HT}^{\leq n}_k denote the assertion that for each kk-coloring cc of N\mathbb{N} there is an infinite set XNX \subseteq \mathbb{N} such that all sums xFx\sum_{x \in F} x for FXF \subseteq X and 0<Fn0 < |F| \leq n have the same color. We prove that there is a computable 22-coloring cc of N\mathbb{N} such that there is no infinite computable set XX such that all nonempty sums of at most 22 elements of XX have the same color. It follows that HT22\mathsf{HT}^{\leq 2}_2 is not provable in RCA0\mathsf{RCA}_0 and in fact we show that it implies SRT22\mathsf{SRT}^2_2 in RCA0\mathsf{RCA}_0. We also show that there is a computable instance of HT33\mathsf{HT}^{\leq 3}_3 with all solutions computing 00'. The proof of this result shows that HT33\mathsf{HT}^{\leq 3}_3 implies ACA0\mathsf{ACA}_0 in RCA0\mathsf{RCA}_0

    A polychromatic Ramsey theory for ordinals

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    The Ramsey degree of an ordinal α is the least number n such that any colouring of the edges of the complete graph on α using finitely many colours contains an n-chromatic clique of order type α. The Ramsey degree exists for any ordinal α < ω ω . We provide an explicit expression for computing the Ramsey degree given α. We further establish a version of this result for automatic structures. In this version the ordinal and the colouring are presentable by finite automata and the clique is additionally required to be regular. The corresponding automatic Ramsey degree turns out to be greater than the set theoretic Ramsey degree. Finally, we demonstrate that a version for computable structures fails

    Polystyrene/clay nanocomposites by atom transfer radical nitroxide coupling chemistry

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    An efficient protocol, atom transfer radical nitroxide coupling chemistry, for the preparation of polymer/clay nanocomposites via grafting-onto strategy with well-defined polymer, which were synthesized via atom transfer radical polymerization, has been described. The radical coupling, taking place between the clay layers, not only leads to attached polymer chains but also to successful nanocomposite formation with highly exfoliated morphology. Copyright © 2012 Wiley Periodicals, Inc

    On FPL configurations with four sets of nested arches

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    The problem of counting the number of Fully Packed Loop (FPL) configurations with four sets of a,b,c,d nested arches is addressed. It is shown that it may be expressed as the problem of enumeration of tilings of a domain of the triangular lattice with a conic singularity. After reexpression in terms of non-intersecting lines, the Lindstr\"om-Gessel-Viennot theorem leads to a formula as a sum of determinants. This is made quite explicit when min(a,b,c,d)=1 or 2. We also find a compact determinant formula which generates the numbers of configurations with b=d.Comment: 22 pages, TeX, 16 figures; a new formula for a generating function adde

    Actin: its cumbersome pilgrimage through cellular compartments

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    In this article, we follow the history of one of the most abundant, most intensely studied proteins of the eukaryotic cells: actin. We report on hallmarks of its discovery, its structural and functional characterization and localization over time, and point to present days’ knowledge on its position as a member of a large family. We focus on the rather puzzling number of diverse functions as proposed for actin as a dual compartment protein. Finally, we venture on some speculations as to its origin

    Partial Recursive Functions and Finality

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    Abstract. We seek universal categorical conditions ensuring the representability of all partial recursive functions. In the category Pfn of sets and partial functions, the natural numbers provide both an initial algebra and a final coalgebra for the functor 1 + −. We recount how finality yields closure of the partial functions on natural numbers under Kleene’s µ-recursion scheme. Noting that Pfn is not cartesian, we then build on work of Paré and Román, obtaining weak initiality and finality conditions on natural numbers algebras in monoidal categories that ensure the (weak) representability of all partial recursive functions. We further obtain some positive results on strong representability. All these results adapt to Kleisli categories of cartesian categories with natural numbers algebras. However, in general, not all partial recursive functions need be strongly representable.

    Distinct Molecular Evolutionary Mechanisms Underlie the Functional Diversification of the Wnt and TGFβ Signaling Pathways

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    The canonical Wnt pathway is one of the oldest and most functionally diverse of animal intercellular signaling pathways. Though much is known about loss-of-function phenotypes for Wnt pathway components in several model organisms, the question of how this pathway achieved its current repertoire of functions has not been addressed. Our phylogenetic analyses of 11 multigene families from five species belonging to distinct phyla, as well as additional analyses employing the 12 Drosophila genomes, suggest frequent gene duplications affecting ligands and receptors as well as co-evolution of new ligand–receptor pairs likely facilitated the expansion of this pathway’s capabilities. Further, several examples of recent gene loss are visible in Drosophila when compared to family members in other phyla. By comparison the TGFβ signaling pathway is characterized by ancient gene duplications of ligands, receptors, and signal transducers with recent duplication events restricted to the vertebrate lineage. Overall, the data suggest that two distinct molecular evolutionary mechanisms can create a functionally diverse developmental signaling pathway. These are the recent dynamic generation of new genes and ligand–receptor interactions as seen in the Wnt pathway and the conservative adaptation of ancient pre-existing genes to new roles as seen in the TGFβ pathway. From a practical perspective, the former mechanism limits the investigator’s ability to transfer knowledge of specific pathway functions across species while the latter facilitates knowledge transfer
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