130 research outputs found

    Two Langevin equations in the Doi-Peliti formalism

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    A system-size expansion method is incorporated into the Doi-Peliti formalism for stochastic chemical kinetics. The basic idea of the incorporation is to introduce a new decomposition of unity associated with a so-called Cole-Hopf transformation. This approach elucidates a relationship between two different Langevin equations; one is associated with a coherent-state path-integral expression and the other describes density fluctuations. A simple reaction scheme X⇄X+XX \rightleftarrows X+X is investigated as an illustrative example.Comment: 14page

    Geometrical tests of cosmological models. I. Probing dark energy using the kinematics of high redshift galaxies

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    We suggest to use the observationally measured and theoretically justified correlation between size and rotational velocity of galactic discs as a viable method to select a set of high redshift standard rods which may be used to explore the dark energy content of the universe via the classical angular-diameter test. Here we explore a new strategy for an optimal implementation of this test.We propose to use the rotation speed of high redshift galaxies as a standard size indicator and show how high resolution multi-object spectroscopy and ACS/HST high quality spatial images, may be combined to measure the amplitude of the dark energy density parameter ΩQ, or to constrain the cosmic equation of state parameter for a smooth dark energy component (w = p/ρ, −1 ≀ w < −1/3). Nearly 1300 standard rods with high velocity rotation in the bin V = 200 ± 20 km s−1 are expected in a field of 1 sq. degree and over the redshift baseline 0 < z < 1.4. This sample is sufficient to constrain the cosmic equation of state parameter w at a level of 20% (without priors in the [Ωm,ΩQ] plane) even when the [OII]λ3727 Å linewidth-diameter relationship is calibrated with a scatter of ∌40%. We evaluate how systematics may affect the proposed tests, and find that a linear standard rod evolution, causing galaxy dimensions to be up to 30% smaller at z = 1.5, can be uniquely diagnosed, and will minimally bias the confidence level contours in the [ΩQ, w] plane. Finally, we show how to derive, without a priori knowing the specific functional form of disc evolution, a cosmologyevolution diagram with which it is possible to establish a mapping between different cosmological models and the amount of galaxy disc/luminosity evolution expected at a given redshift

    Differential branching fraction and angular analysis of the decay B0→K∗0ÎŒ+Ό−

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    The angular distribution and differential branching fraction of the decay B 0→ K ∗0 ÎŒ + ÎŒ − are studied using a data sample, collected by the LHCb experiment in pp collisions at s√=7 TeV, corresponding to an integrated luminosity of 1.0 fb−1. Several angular observables are measured in bins of the dimuon invariant mass squared, q 2. A first measurement of the zero-crossing point of the forward-backward asymmetry of the dimuon system is also presented. The zero-crossing point is measured to be q20=4.9±0.9GeV2/c4 , where the uncertainty is the sum of statistical and systematic uncertainties. The results are consistent with the Standard Model predictions

    Measurements of the branching fractions of the decays B°s → D∓s K± and B°s → DÂŻsπ+

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    The decay mode B°s → D∓s K± allows for one of the theoretically cleanest measurements of the CKM angle Îł through the study of time-dependent CP violation. This paper reports a measurement of its branching fraction relative to the Cabibbo-favoured mode B°s → DÂŻsπ+ based on a data sample corresponding to 0.37 fbÂŻÂč of proton-proton collisions at √s = 7TeV collected in 2011 with the LHCb detector. In addition, the ratio of B meson production fractions fs/fd, determined from semileptonic decays, together with the known branching fraction of the control channel B°s → DÂŻsπ+ is used to perform an absolute measurement of the branching fractions: B(B°s → DÂŻsπ+) = (2.95 ± 0.05 ± 0.17 -0.22 +0.18) × 10ÂŻÂł ; B(B°s → D∓s K±) = (1.90 ± 0.12 ± 0.13 -0.14 +0.12) × 10ÂŻ4 ; where the first uncertainty is statistical, the second the experimental systematic uncertainty, and the third the uncertainty due to f s/f

    Measurement of the CP-violating phase phi_s in the decay Bs->J/psi phi

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    We present a measurement of the time-dependent CP-violating asymmetry in B_s -> J/psi phi decays, using data collected with the LHCb detector at the LHC. The decay time distribution of B_s -> J/psi phi is characterized by the decay widths Gamma_H and Gamma_L of the heavy and light mass eigenstates of the B_s-B_s-bar system and by a CP-violating phase phi_s. In a sample of about 8500 B_s -> J/psi phi events isolated from 0.37 fb^-1 of pp collisions at sqrt(s)=7 TeV we measure phi_s = 0.15 +/- 0.18 (stat) +/- 0.06 (syst) rad. We also find an average B_s decay width Gamma_s == (Gamma_L + Gamma_H)/2 = 0.657 +/- 0.009 (stat) +/- 0.008 (syst) ps^-1 and a decay width difference Delta Gamma_s == Gamma_L - Gamma_H} = 0.123 +/- 0.029 (stat) +/- 0.011 (syst) ps^-1. Our measurement is insensitive to the transformation (phi_s,DeltaGamma_s --> pi - phi_s, - Delta Gamma_s.Comment: 9 pages, 3 figure

    Strong constraints on the rare decays Bs -> mu+ mu- and B0 -> mu+ mu-

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    A search for Bs -> mu+ mu- and B0 -> mu+ mu- decays is performed using 1.0 fb^-1 of pp collision data collected at \sqrt{s}=7 TeV with the LHCb experiment at the Large Hadron Collider. For both decays the number of observed events is consistent with expectation from background and Standard Model signal predictions. Upper limits on the branching fractions are determined to be BR(Bs -> mu+ mu-) mu+ mu-) < 1.0 (0.81) x 10^-9 at 95% (90%) confidence level.Comment: 2+6 pages; 4 figures; Accepted for publication in Physical Review Letter

    Observation of the decay Bc→J/ψK+K−π+B_c \rightarrow J/\psi K^+ K^- \pi^+

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    The decay Bc→J/ψK+K−π+B_c\rightarrow J/\psi K^+ K^- \pi^+ is observed for the first time, using proton-proton collisions collected with the LHCb detector corresponding to an integrated luminosity of 3fb−1^{-1}. A signal yield of 78±1478\pm14 decays is reported with a significance of 6.2 standard deviations. The ratio of the branching fraction of \B_c \rightarrow J/\psi K^+ K^- \pi^+ decays to that of Bc→J/ψπ+B_c \rightarrow J/\psi \pi^+ decays is measured to be 0.53±0.10±0.050.53\pm 0.10\pm0.05, where the first uncertainty is statistical and the second is systematic.Comment: 18 pages, 2 figure

    CoartemÂź: the journey to the clinic

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    Artemisinin, from which the artemether component of CoartemÂź(artemether/lumefantrine, AL) is derived, is obtained from the plant sweet wormwood (Artemisia annua) which has been used for over 2,000 years as a Chinese herbal remedy. Artemisinin was first identified by Chinese researchers as the active anti-malarial constituent of A. annua and its derivatives were found to be the most potent of all anti-malarial drugs. Artemether acts rapidly, reducing the infecting parasite biomass by approximately 10,000-fold per asexual life cycle. Lumefantrine, the other active constituent of AL, acts over a longer period to eliminate the residual 100-100,000 parasites that remain after artemether is cleared from the body and thus minimizes the risk of recrudescence. The two agents have different modes of action and act at different points in the parasite life cycle and show a synergistic action against Plasmodium falciparum in vitro. The combination of artemether and lumefantrine reduces the risk of resistance developing to either agent, and to date there are no reports of resistance to AL combined therapy in the malaria parasite that infects humans. Following a unique partnership agreement between Chinese authorities and Novartis, the manufacturer of AL, over 20 sponsored clinical studies have been undertaken in various malaria endemic regions and in travellers. These trials have involved more than 3,500 patients (including over 2,000 children), and led to identification of a six-dose, three-day regimen as the optimal dosing strategy for AL in uncomplicated falciparum malaria. AL has consistently shown 28-day polymerase chain (PCR)-corrected cure rates greater than 95% in the evaluable population, meeting WHO recommendations. More recently, Novartis and the Medicines for Malaria Venture have worked in partnership to develop CoartemÂź Dispersible, a new formulation designed specifically to meet the specific needs of children with malaria. The dispersible tablets have shown similar high response rates to those observed with crushed standard tablets of AL. A partnership agreement between Novartis and WHO has seen over 250 million AL (CoartemÂź) treatments (75% for children) being distributed to malaria patients in developing countries without profit, supported by training programmes and educational resources

    Combining Fungal Biopesticides and Insecticide-Treated Bednets to Enhance Malaria Control

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    In developing strategies to control malaria vectors, there is increased interest in biological methods that do not cause instant vector mortality, but have sublethal and lethal effects at different ages and stages in the mosquito life cycle. These techniques, particularly if integrated with other vector control interventions, may produce substantial reductions in malaria transmission due to the total effect of alterations to multiple life history parameters at relevant points in the life-cycle and transmission-cycle of the vector. To quantify this effect, an analytically tractable gonotrophic cycle model of mosquito-malaria interactions is developed that unites existing continuous and discrete feeding cycle approaches. As a case study, the combined use of fungal biopesticides and insecticide treated bednets (ITNs) is considered. Low values of the equilibrium EIR and human prevalence were obtained when fungal biopesticides and ITNs were combined, even for scenarios where each intervention acting alone had relatively little impact. The effect of the combined interventions on the equilibrium EIR was at least as strong as the multiplicative effect of both interventions. For scenarios representing difficult conditions for malaria control, due to high transmission intensity and widespread insecticide resistance, the effect of the combined interventions on the equilibrium EIR was greater than the multiplicative effect, as a result of synergistic interactions between the interventions. Fungal biopesticide application was found to be most effective when ITN coverage was high, producing significant reductions in equilibrium prevalence for low levels of biopesticide coverage. By incorporating biological mechanisms relevant to vectorial capacity, continuous-time vector population models can increase their applicability to integrated vector management
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