89 research outputs found

    The Influence of Sex and Fly Species on the Development of Trypanosomes in Tsetse Flies

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    Unlike other dipteran disease vectors, tsetse flies of both sexes feed on blood and transmit pathogenic African trypanosomes. During transmission, Trypanosoma brucei undergoes a complex cycle of proliferation and development inside the tsetse vector, culminating in production of infective forms in the saliva. The insect manifests robust immune defences throughout the alimentary tract, which eliminate many trypanosome infections. Previous work has shown that fly sex influences susceptibility to trypanosome infection as males show higher rates of salivary gland (SG) infection with T. brucei than females. To investigate sex-linked differences in the progression of infection, we compared midgut (MG), proventriculus, foregut and SG infections in male and female Glossina morsitans morsitans. Initially, infections developed in the same way in both sexes: no difference was observed in numbers of MG or proventriculus infections, or in the number and type of developmental forms produced. Female flies tended to produce foregut migratory forms later than males, but this had no detectable impact on the number of SG infections. The sex difference was not apparent until the final stage of SG invasion and colonisation, showing that the SG environment differs between male and female flies. Comparison of G. m. morsitans with G. pallidipes showed a similar, though less pronounced, sex difference in susceptibility, but additionally revealed very different levels of trypanosome resistance in the MG and SG. While G. pallidipes was more refractory to MG infection, a very high proportion of MG infections led to SG infection in both sexes. It appears that the two fly species use different strategies to block trypanosome infection: G. pallidipes heavily defends against initial establishment in the MG, while G. m. morsitans has additional measures to prevent trypanosomes colonising the SG, particularly in female flies. We conclude that the tsetse-trypanosome interface works differently in G. m. morsitans and G. pallidipes

    Higher-order multipole amplitude measurement in ψ ′→γχ c2

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    Using 106×106 ψ ′ events collected with the BESIII detector at the BEPCII storage ring, the higher-order multipole amplitudes in the radiative transition ψ ′→γχ c2→γπ +π -/γK +K - are measured. A fit to the χ c2 production and decay angular distributions yields M2=0.046±0. 010±0.013 and E3=0.015±0.008±0.018, where the first errors are statistical and the second systematic. Here M2 denotes the normalized magnetic quadrupole amplitude and E3 the normalized electric octupole amplitude. This measurement shows evidence for the existence of the M2 signal with 4.4σ statistical significance and is consistent with the charm quark having no anomalous magnetic moment. © 2011 American Physical Society.published_or_final_versio

    Study of a00(980)-f0(980) mixing

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    Using samples of 2.25×108 J/ψ events and 1.06×108 ψ ′ events collected with the BES III detector, we study the f 0(980)→a00(980) and a00(980)→f 0(980) transitions in the processes J/ψ→φf 0(980) →φa00(980) and χ c1→π0a00(980)→π0f 0(980), respectively. Evidence for f 0(980)→a00(980) is found with a significance of 3.4σ, while in the case of a00(980)→f 0(980) transition, the significance is 1.9σ. Measurements and upper limits of both branching ratios and mixing intensities are determined. © 2011 American Physical Society.published_or_final_versio

    Two-photon widths of the χ c0,2 states and helicity analysis for χ c2→γγ

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    Based on a data sample of 106×106 ψ ′ events collected with the BESIII detector, the decays ψ ′→γχ c0,2, χ c0,2→γγ are studied to determine the two-photon widths of the χ c0,2 states. The two-photon decay branching fractions are determined to be B(χ c0→γγ)=(2. 24±0.19±0.12±0.08)×10 -4 and B(χ c2→γγ)=(3.21±0.18±0. 17±0.13)×10 -4. From these, the two-photon widths are determined to be Γ γγ(χ c0)=(2. 33±0.20±0.13±0.17)keV, Γ γγ(χ c2)=(0.63±0.04±0. 04±0.04)keV, and R=Γ γγ(χ c2)/ Γ γγ(χ c0)=0.271±0. 029±0.013±0.027, where the uncertainties are statistical, systematic, and those from the PDG B(ψ ′→γχ c0,2) and Γ(χ c0,2) errors, respectively. The ratio of the two-photon widths for helicity λ=0 and helicity λ=2 components in the decay χ c2→γγ is measured for the first time to be f 0/2=Γγγλ= 0(χ c2)/Γγγλ=2(χ c2)=0. 00±0.02±0.02. © 2012 American Physical Society.published_or_final_versio

    Observation of \chi_{cJ} decaying into the p\bar{p}K^{+}K^{-} final state

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    First measurements of the decays of the three χcJ\chi_{cJ} states to ppˉK+K−p\bar{p}K^{+}K^{-} final states are presented. Intermediate ϕ→K+K−\phi\to K^{+}K^{-} and Λ(1520)→pK−\Lambda(1520)\to pK^{-} resonance states are observed, and branching fractions for χcJ→pˉK+Λ(1520)\chi_{cJ}\to \bar{p}K^{+}\Lambda(1520), Λ(1520)Λˉ(1520)\Lambda(1520) \bar{\Lambda}(1520), and ϕppˉ\phi p\bar{p} are reported. We also measure branching fractions for direct χcJ→ppˉK+K−\chi_{cJ}\to p\bar{p} K^{+}K^{-} decays. These are first observations of χcJ\chi_{cJ} decays to unstable baryon resonances and provide useful information about the χcJ\chi_{cJ} states. The experiment uses samples of χcJ\chi_{cJ} mesons produced via radiative transitions from 106 million ψ′\psi^{\prime} mesons collected in the BESIII detector at the BEPCII e+e−e^+e^- collider.Comment: 16 pages, 5 figure

    Evidence for psi' decays into gamma pi^0 and gamma eta

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    The decays psi'->gamma pi^0, gamma eta and gamma eta' are studied using data collected with the BESIII detector at the BEPCII e^+e^- collider. Processes psi'->gamma pi^0 and psi'->gamma eta are observed for the first time with signal significances of 4.6 sigma and 4.3 sigma, respectively. The branching fractions are determined to be: B(psi'->gamma pi^0)=(1.58+-0.40+-0.13)x10^{-6}, B(psi'->gamma eta)=(1.38+-0.48+-0.09)x10^{-6}, and B(psi'->gamma eta')=(126+-3+-8) x 10^{-6}, where the first errors are statistical and the second ones systematic.Comment: 6 pages, 4 figure
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