3,528 research outputs found

    An exact sequence for contact- and symplectic homology

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    A symplectic manifold WW with contact type boundary M=WM = \partial W induces a linearization of the contact homology of MM with corresponding linearized contact homology HC(M)HC(M). We establish a Gysin-type exact sequence in which the symplectic homology SH(W)SH(W) of WW maps to HC(M)HC(M), which in turn maps to HC(M)HC(M), by a map of degree -2, which then maps to SH(W)SH(W). Furthermore, we give a description of the degree -2 map in terms of rational holomorphic curves with constrained asymptotic markers, in the symplectization of MM.Comment: Final version. Changes for v2: Proof of main theorem supplemented with detailed discussion of continuation maps. Description of degree -2 map rewritten with emphasis on asymptotic markers. Sec. 5.2 rewritten with emphasis on 0-dim. moduli spaces. Transversality discussion reorganized for clarity (now Remark 9). Various other minor modification

    Biotic and abiotic factors influencing the mangrove vegetation of Qaoqiang (Guangdong, China): a first approach

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    The present ongoing MSc study is carried out in south-western China, in a mangrove managed by the Zhanjiang Mangrove National Natural Reserve (ZMNNR). The ZMNNR covers approximately 20,000ha of naturally established mangrove forest, mangrove plantations, inter-tidal sand and mud flats, river channels and streams. The reserve has been classified in 2002 as a wetland of national importance by the Ramsar Convention for its biodiversity, for the goods and services provided to the population and also as a bird refuge of great importance. However, this area is still relatively unknown, and not much phytosociological studies were carried out there. The mangrove we are studying is located in the County of Lianjiang: an enclave in the Beibu Gulf, at 4.5km to the southwest of the town of Gaoqiao. The Gaoqiao mangrove is the most important wetland area managed by the ZMNNR. The aim of this study is to understand and analyse the structure of the vegetation in terms of floristic diversity, biomass, density and height of the trees based on nine transects with a total of 210 sampled points. The structure of the vegetation will be determined with beta diversity index, biomass, height and basal area of trees for each of the sampling point. Then we will apply a multivariate analysis (ordination, cluster and statistical analysis) to find which of the selected environmental factors can explain the most part of the vegetation. Each analysis will be done for two phytosociological methods: a plot-based method and a plot-less method. We will test the relationship between these sampling methods to find an appropriate compromise between accuracy and time spent on it. Other observations were also made in this newly studied mangrove. New researches will be done soon on the parasitism of mangrove trees by barnacles and caterpillars, on the invasion of exotic introduced species, on fishing impact, aquaculture and rice culture, on the climate impacts and on the importance of the rivers network on the vegetation structure and dynamics

    The Minimal Length of a Lagrangian Cobordism between Legendrians

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    To investigate the rigidity and flexibility of Lagrangian cobordisms between Legendrian submanifolds, we investigate the minimal length of such a cobordism, which is a 11-dimensional measurement of the non-cylindrical portion of the cobordism. Our primary tool is a set of real-valued capacities for a Legendrian submanifold, which are derived from a filtered version of Legendrian Contact Homology. Relationships between capacities of Legendrians at the ends of a Lagrangian cobordism yield lower bounds on the length of the cobordism. We apply the capacities to Lagrangian cobordisms realizing vertical dilations (which may be arbitrarily short) and contractions (whose lengths are bounded below). We also study the interaction between length and the linking of multiple cobordisms as well as the lengths of cobordisms derived from non-trivial loops of Legendrian isotopies.Comment: 33 pages, 9 figures. v2: Minor corrections in response to referee comments. More general statement in Proposition 3.3 and some reorganization at the end of Section

    New obstructions to symplectic embeddings

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    In this paper we establish new restrictions on symplectic embeddings of certain convex domains into symplectic vector spaces. These restrictions are stronger than those implied by the Ekeland-Hofer capacities. By refining an embedding technique due to Guth, we also show that they are sharp.Comment: 80 pages, 3 figures, v2: improved exposition and minor corrections, v3: Final version, expanded and improved exposition and minor corrections. The final publication is available at link.springer.co

    Proteomic identification of heterogeneous nuclear ribonucleoprotein L as a novel component of SLM/Sam68 nuclear bodies

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    Background: Active pre-mRNA splicing occurs co-transcriptionally, and takes place throughout the nucleoplasm of eukaryotic cells. Splicing decisions are controlled by networks of nuclear RNA-binding proteins and their target sequences, sometimes in response to signalling pathways. Sam68 (Src-associated in mitosis 68 kDa) is the prototypic member of the STAR (Signal Transduction and Activation of RNA) family of RNA-binding proteins, which regulate splicing in response to signalling cascades. Nuclear Sam68 protein is concentrated within subnuclear organelles called SLM/Sam68 Nuclear Bodies (SNBs), which also contain some other splicing regulators, signalling components and nucleic acids. Results: We used proteomics to search for the major interacting protein partners of nuclear Sam68. In addition to Sam68 itself and known Sam68-associated proteins (heterogeneous nuclear ribonucleoproteins hnRNP A1, A2/B1 and G), we identified hnRNP L as a novel Sam68-interacting protein partner. hnRNP L protein was predominantly present within small nuclear protein complexes approximating to the expected size of monomers and dimers, and was quantitatively associated with nucleic acids. hnRNP L spatially co-localised with Sam68 as a novel component of SNBs and was also observed within the general nucleoplasm. Localisation within SNBs was highly specific to hnRNP L and was not shared by the closely-related hnRNP LL protein, nor any of the other Sam68-interacting proteins we identified by proteomics. The interaction between Sam68 and hnRNP L proteins was observed in a cell line which exhibits low frequency of SNBs suggesting that this association also takes place outside SNBs. Although ectopic expression of hnRNP L and Sam68 proteins independently affected splicing of CD44 variable exon v5 and TJP1 exon 20 minigenes, these proteins did not, however, co-operate with each other in splicing regulation of these target exons. Conclusion: Here we identify hnRNP L as a novel SNB component. We show that, compared with other identified Sam68-associated hnRNP proteins and hnRNP LL, this co-localisation within SNBs is specific to hnRNP L. Our data suggest that the novel Sam68-hnRNP L protein interaction may have a distinct role within SNBs

    Evidence for the role of normal-state electrons in nanoelectromechanical damping mechanisms at very low temperatures

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    We report on experiments performed at low temperatures on aluminum covered silicon nanoelectromechanical resonators. The substantial difference observed between the mechanical dissipation in the normal and superconducting states measured within the same device unambiguously demonstrates the importance of normal-state electrons in the damping mechanism. The dissipative component becomes vanishingly small at very low temperatures in the superconducting state, leading to exceptional values for the quality factor of such small silicon structures. A critical discussion is given within the framework of the standard tunneling model

    Parameterized Algorithms for Graph Partitioning Problems

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    We study a broad class of graph partitioning problems, where each problem is specified by a graph G=(V,E)G=(V,E), and parameters kk and pp. We seek a subset UVU\subseteq V of size kk, such that α1m1+α2m2\alpha_1m_1 + \alpha_2m_2 is at most (or at least) pp, where α1,α2R\alpha_1,\alpha_2\in\mathbb{R} are constants defining the problem, and m1,m2m_1, m_2 are the cardinalities of the edge sets having both endpoints, and exactly one endpoint, in UU, respectively. This class of fixed cardinality graph partitioning problems (FGPP) encompasses Max (k,nk)(k,n-k)-Cut, Min kk-Vertex Cover, kk-Densest Subgraph, and kk-Sparsest Subgraph. Our main result is an O(4k+o(k)Δk)O^*(4^{k+o(k)}\Delta^k) algorithm for any problem in this class, where Δ1\Delta \geq 1 is the maximum degree in the input graph. This resolves an open question posed by Bonnet et al. [IPEC 2013]. We obtain faster algorithms for certain subclasses of FGPPs, parameterized by pp, or by (k+p)(k+p). In particular, we give an O(4p+o(p))O^*(4^{p+o(p)}) time algorithm for Max (k,nk)(k,n-k)-Cut, thus improving significantly the best known O(pp)O^*(p^p) time algorithm
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