74 research outputs found

    Some results on the saturation number for unions of cliques

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    Graph GG is HH-saturated if HH is not a subgraph of GG and HH is a subgraph of G+eG+e for any edge ee not in GG. The saturation number for a graph HH is the minimal number of edges in any HH-saturated graph of order nn. In this paper, the saturation number for Kp∪(t−1)KqK_p\cup (t-1)K_q (t⩾3t\geqslant 3 and 2⩽p<q2\leqslant p<q) is determined, and the extremal graph for Kp∪2KqK_p\cup 2K_q is determined. Moreover, the saturation number and the extremal graph for Kp∪Kq∪KrK_p\cup K_q\cup K_r (r⩾p+q r\geqslant p+q) are completely determined

    EDDA: An Efficient Distributed Data Replication Algorithm in VANETs

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    Efficient data dissemination in vehicular ad hoc networks (VANETs) is a challenging issue due to the dynamic nature of the network. To improve the performance of data dissemination, we study distributed data replication algorithms in VANETs for exchanging information and computing in an arbitrarily-connected network of vehicle nodes. To achieve low dissemination delay and improve the network performance, we control the number of message copies that can be disseminated in the network and then propose an efficient distributed data replication algorithm (EDDA). The key idea is to let the data carrier distribute the data dissemination tasks to multiple nodes to speed up the dissemination process. We calculate the number of communication stages for the network to enter into a balanced status and show that the proposed distributed algorithm can converge to a consensus in a small number of communication stages. Most of the theoretical results described in this paper are to study the complexity of network convergence. The lower bound and upper bound are also provided in the analysis of the algorithm. Simulation results show that the proposed EDDA can efficiently disseminate messages to vehicles in a specific area with low dissemination delay and system overhead

    Observation of Hybrid-Order Topological Pump in a Kekule-Textured Graphene Lattice

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    Thouless charge pumping protocol provides an effective route for realizing topological particle transport. To date, the first-order and higher-order topological pumps, exhibiting transitions of edge-bulk-edge and corner-bulk-corner states, respectively, are observed in a variety of experimental platforms. Here, we propose a concept of hybrid-order topological pump, which involves a transition of bulk, edge, and corner states simultaneously. More specifically, we consider a Kekul\'e-textured graphene lattice that features a tunable phase parameter. The finite sample of zigzag boundaries, where the corner configuration is abnormal and inaccessible by repeating unit cells, hosts topological responses at both the edges and corners. The former is protected by a nonzero winding number, while the latter can be explained by a nontrivial vector Chern number. Using our skillful acoustic experiments, we verify those nontrivial boundary landmarks and visualize the consequent hybrid-order topological pump process directly. This work deepens our understanding to higher-order topological phases and broadens the scope of topological pumps.Comment: 5 figure

    Immune Monitoring of Trans-endothelial Transport by Kidney-Resident Macrophages

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    Small immune complexes cause type III hypersensitivity reactions that frequently result in tissue injury. The responsible mechanisms however remain unclear and differ depending on target organs. Here we identify a kidney-specific anatomical and functional unit, formed by resident macrophages and peritubular capillary endothelial cells, which monitors the transport of proteins and particles ranging from 20 to 700 kDa or 10 to 200 nm into the kidney interstitium. Kidney resident macrophages detect and scavenge circulating immune complexes ‘pumped’ into the interstitium via trans-endothelial transport, and trigger a FcγRIV-dependent inflammatory response and the recruitment of monocytes and neutrophils. In addition, FcγRIV and TLR pathways synergistically ‘super-activate’ kidney macrophages when immune complexes contain a nucleic acid. These data identify a physiological function of tissue resident kidney macrophages and a basic mechanism by which they initiate the inflammatory response to small immune complexes in the kidney

    Keragaman Genetik Dan Pendugaan Jumlah Gen Ketahanan Kacang Panjang (Vigna Sinensis L.) Terhadap Penyakit Kuning

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    Penyakit kuning pada kacang panjang berdampak pada penurunan produksi. Gejala serangan diawali dari gejala daun keriting serta mengakibatkan polong berwarna kuning. Penelitian ini bertujuan mengetahui nilai heritabilitas dan ragam genetik serta menduga jumlah gen pengendali ketahanan kacang panjang terhadap penyakit kuning. Penelitian dilaksanakan di Kabupaten Kediri pada bulan April sampai Juli 2013. Bahan penelitian adalah populasi UB 715 A (P1), Hitam Putih (P2), populasi F1 dan populasi F2. Berdasarkan hasil penelitian, populasi UB 715 A (P1 ) menunjukkan respon tahan terhadap penyakit kuning, populasi Hitam Putih (P2) menunjukkan respon rentan, dan populasi F1 dan F2 menunjukkan respon sedang. Karakter jumlah polong dan jumlah biji per tanaman memiliki keragaman yang sempit sedangkan karakter panjang polong, bobot segar polong, umur berbunga, dan umur panen memiliki keragaman yang luas. Karakter panjang polong dan jumlah biji per polong memiliki nilai heritabilitas rendah, sedangkan karakter jumlah polong, bobot segar polong, umur berbunga, dan umur panen memiliki nilai heritabilitas tinggi. Rasio sifat ketahanan terhadap penyakit kuning pada populasi F2 adalah 9 tahan : 3 sedang : 4 rentan yang berarti ketahanan terhadap penyakit kuning dikendalikan oleh dua gen dengan aksi gen epistasis resesif

    An essential role for the IL-2 receptor in Treg cell function

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    Regulatory T cells (Treg cells), which have abundant expression of the interleukin 2 receptor (IL-2R), are reliant on IL-2 produced by activated T cells. This feature indicates a key role for a simple network based on the consumption of IL-2 by Treg cells in their suppressor function. However, congenital deficiency in IL-2R results in reduced expression of the Treg cell lineage–specification factor Foxp3, which has confounded experimental efforts to understand the role of IL-2R expression and signaling in the suppressor function of Treg cells. Using genetic gain- and loss-of-function approaches, we found that capture of IL-2 was dispensable for the control of CD4+ T cells but was important for limiting the activation of CD8+ T cells, and that IL-2R-dependent activation of the transcription factor STAT5 had an essential role in the suppressor function of Treg cells separable from signaling via the T cell antigen receptor
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