360 research outputs found

    Double loop networks with minimum delay

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    AbstractDouble loop networks have been widely studied as practical and reliable computer networks. Let N denote the number of stations in a double loop network. The literature has proposed a topology which yields the diameter 2√N. In this paper we give a heuristic method which finds a topology with diameter roughly √3N for large N. We also give several infinite classes of values of N for which topologies are found that achieve the lower bound ⌈√3N⌉ − 2 for the diameter

    Responses of Helicoverpa armigera to tomato plants previously infected by ToMV or damaged by H-Armigera

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    We report the comparative inducing effects of a phytopathogen and a herbivorous arthropod on the performance of an herbivore. Tomato, Lycopersicon esculentum Mill., was used as the test plant, and tomato mosaic virus (ToMV) and corn earworm, Helicoverpa armigera Hubner, were used as the phytopathogen and herbivore, respectively. There were decreases in the efficiency of conversion of ingested food and efficiency of conversion of digested food when H. armigera was reared on tomato plants that had been previously inoculated with ToMV. However, virus inoculation did not affect feeding or oviposition preferences by H. armigera. In contrast, approximate digestibility, total consumption, relative growth rate, and relative consumption rate were lower for fourth-instar H. armigera that fed on plants previously damaged by the same herbivore. Feeding and oviposition were both deterred for H. armigera that fed on previously damaged plants. The duration of development of H. armigera was also prolonged under this treatment. Infection by ToMV and feeding damage by H. armigera increased the host plant's peroxidase and polyphenol oxidase activity, respectively, suggesting that the performance of H. armigera may be affected by the induced phytochemistry of the host plant. Overall, this study indicated that, in general, insect damage has a stronger effect than ToMV infection on plant chemistry and, subsequently, on the performance of H. armigera

    Immunolocalization of chloride transporters to gill epithelia of euryhaline teleosts with opposite salinity-induced Na+/K+-ATPase responses

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    Opposite patterns of branchial Na+/K+-ATPase (NKA) responses were found in euryhaline milkfish (Chanos chanos) and pufferfish (Tetraodon nigroviridis) upon salinity challenge. Because the electrochemical gradient established by NKA is thought to be the driving force for transcellular Cl- transport in fish gills, the aim of this study was to explore whether the differential patterns of NKA responses found in milkfish and pufferfish would lead to distinct distribution of Cl- transporters in their gill epithelial cells indicating different Cl- transport mechanisms. In this study, immunolocalization of various Cl- transport proteins, including Na+/K+/2Cl(-) cotransporter (NKCC), cystic fibrosis transmembrane conductance regulator (CFTR), anion exchanger 1 (AE1), and chloride channel 3 (ClC-3), were double stained with NKA, the basolateral marker of branchial mitochondrion-rich cells (MRCs), to reveal the localization of these transporter proteins in gill MRC of FW- or SW-acclimated milkfish and pufferfish. Confocal microscopic observations showed that the localization of these transport proteins in the gill MRCs of the two studied species were similar. However, the number of gill NKA-immunoreactive (IR) cells in milkfish and pufferfish exhibited to vary with environmental salinities. An increase in the number of NKA-IR cells should lead to the elevation of NKA activity in FW milkfish and SW pufferfish. Taken together, the opposite branchial NKA responses observed in milkfish and pufferfish upon salinity challenge could be attributed to alterations in the number of NKA-IR cells. Furthermore, the localization of these Cl- transporters in gill MRCs of the two studied species was identical. It depicted the two studied euryhaline species possess the similar Cl- transport mechanisms in gills

    Baculovirus Transduction of Mesenchymal Stem Cells: In Vitro Responses and In Vivo Immune Responses After Cell Transplantation

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    Baculovirus holds great promise for the genetic modification of mesenchymal stem cells (MSCs). However, whether baculovirus transduction provokes undesired MSCs responses that might compromise their in vivo applications has yet to be examined. Hereby, we unraveled that baculovirus transduction of human MSCs upregulated the transcription of interleukin (IL)-1 beta, interferon (IFN)-alpha and IL-6, but not tumor necrosis factor (TNF)-alpha and IFN-gamma. However, only IL-6 secretion was detectable by enzyme-linked immunosorbent assay (ELISA). Baculovirus transduction also stimulated transient, low level upregulation of human leukocyte antigen I (HLA-I) on the human MSCs surface, yet it did not either altered the HLA-II expression or impaired the MSCs ability to inhibit lymphocyte proliferation. After transplantation into allogeneic rats, the transduced rat MSCs elicited transient, mild macrophage responses, but the cells remained tolerant as judged by the persistence of transplanted cells and absence of CD8(+) T cells infiltration. Besides, transplantation of the transduced MSCs did not provoke systemic induction of monocytes and CD8(+) T cells. This study, for the first time, explores the responses of MSCs to virus transduction and confirms the safety of transplanting baculovirus-engineered MSCs into immunocompetent animals for cell-based gene therapy

    Acoustic and relaxation processes in supercooled o-ter-phenyl by optical-heterodyne transient grating experiment

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    The dynamics of the fragile glass-forming o-ter-phenyl is investigated by time-resolved transient grating experiment with an heterodyne detection technique in a wide temperature range. We investigated the dynamics processes of this glass-former over more then 6 decades in time with an excellent signal/noise. Acoustic, structural and thermal relaxations have been clearly identify and measured in a time-frequency window not covered by previous spectroscopic investigations. A detailed comparison with the density response function, calculated on the basis of generalized hydrodynamics model, has been worked out

    B -> J/psi K^* Decays in QCD Factorization

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    The hadronic decay B -> J K^* is analyzed within the framework of QCD factorization. The spin amplitudes A_0, A_\parallel and A_\perp in the transversity basis and their relative phases are studied using various different form-factor models for B-K^* transition. The effective parameters a_2^h for helicity h=0,+,- states receive different nonfactorizable contributions and hence they are helicity dependent, contrary to naive factorization where a_2^h are universal and polarization independent. QCD factorization breaks down even at the twist-2 level for transverse hard spectator interactions. Although a nontrivial strong phase for the A_\parallel amplitude can be achieved by adjusting the phase of an infrared divergent contribution, the present QCD factorization calculation cannot say anything definite about the phase phi_\parallel. Unlike B -> J/psi K decays, the longitudinal parameter a_2^0 for B -> J/psi K^* does not receive twist-3 corrections and is not large enough to account for the observed branching ratio and the fraction of longitudinal polarization. Possible enhancement mechanisms for a_2^0 are discussed.Comment: 21 pages, 1 figure, a table and a reference added, some typos correcte

    Updated Analysis of a_1 and a_2 in Hadronic Two-body Decays of B Mesons

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    Using the recent experimental data of BD()(π,ρ)B\to D^{(*)}(\pi,\rho), BD()Ds()B\to D^{(*)} D_s^{(*)}, BJ/ψK()B\to J/\psi K^{(*)} and various model calculations on form factors, we re-analyze the effective coefficients a_1 and a_2 and their ratio. QCD and electroweak penguin corrections to a_1 from BD()Ds()B\to D^{(*)}D_s^{(*)} and a_2 from BJ/ψK()B\to J/\psi K^{(*)} are estimated. In addition to the model-dependent determination, the effective coefficient a_1 is also extracted in a model-independent way as the decay modes BD()hB\to D^{(*)}h are related by factorization to the measured semileptonic distribution of BD()νˉB\to D^{(*)}\ell \bar\nu at q2=mh2q^2=m_h^2. Moreover, this enables us to extract model-independent heavy-to-heavy form factors, for example, F0BD(mπ2)=0.66±0.06±0.05F_0^{BD}(m_\pi^2)=0.66\pm0.06\pm0.05 and A0BD(mπ2)=0.56±0.03±0.04A_0^{BD^*}(m_\pi^2)=0.56\pm0.03\pm0.04. The determination of the magnitude of a_2 from BJ/ψK()B\to J/\psi K^{(*)} depends on the form factors F1BKF_1^{BK}, A1,2BKA_{1,2}^{BK^*} and VBKV^{BK^*} at q2=mJ/ψ2q^2=m^2_{J/\psi}. By requiring that a_2 be process insensitive (i.e., the value of a_2 extracted from J/ψKJ/\psi K and J/ψKJ/\psi K^* states should be similar), as implied by the factorization hypothesis, we find that BK()B\to K^{(*)} form factors are severely constrained; they respect the relation F1BK(mJ/ψ2)1.9A1BK(mJ/ψ2)F_1^{BK}(m^2_{J/\psi})\approx 1.9 A_1^{BK^*}(m^2_{J/\psi}). Form factors A2BKA_2^{BK^*} and VBKV^{BK^*} at q2=mJ/ψ2q^2=m^2_{J/\psi} inferred from the measurements of the longitudinal polarization fraction and the P-wave component in BJ/ψKB\to J/\psi K^* are obtained. A stringent upper limit on a_2 is derived from the current bound on \ov B^0\to D^0\pi^0 and it is sensitive to final-state interactions.Comment: 33 pages, 2 figures. Typos in Tables I and IX are corrected. To appear in Phys. Rev.
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