5,499 research outputs found

    Observations of Dispersion Cancellation of Entangled Photon Pairs

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    An experimental study of the dispersion cancellation occurring in frequency-entangled photon pairs is presented. The approach uses time-resolved up conversion of the pairs, which has temporal resolution at the fs level, and group-delay dispersion sensitivity of  20fs2\approx \ 20 \, \mathrm{fs}^2 under experimental conditions. The cancellation is demonstrated with dispersion stronger than ±103fs2\pm 10^3 \, \mathrm{fs}^2 in the signal ()(-) and idler (+)(+) modes. The observations represent the generation, compression, and characterization of ultrashort biphotons with correlation width as small as 6.8 times the degenerate optical period.Comment: 5 pages, 3 figure

    Moving beyond the ‘language problem': developing an understanding of the intersections of health, language and immigration status in interpreter-mediated health encounters

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    Health systems internationally are dealing with greater diversity in patient populations. However the focus on ‘the language problem’ has meant little attention is paid to diversity within and between migrant populations; and how interpreted consultations are influenced by intersecting migratory, ethnicity and sociodemographic variables. Our analysis of the experiences of patients, health care providers and interpreters in Scotland evidences the need to move beyond language, addressing multiple hidden inequalities in health care access and provision that operate in both clinic and, especially, home-based settings. We call for a practice-evidenced research agenda promoting cultural communication across health care and home settings, acknowledging immigration status as a social determinant of health. Sur le plan international, des systèmes de santé font face à une diversité croissante dans ses populations de patients. Cependant, l’accent sur ‘le problème de langue’ se traduit dans une manque d’attention à la diversité a l’intérieur même et entre des populations des migrants; et la façon par laquelle des variables migratoire, ethnique et sociodémographique influencent elles-mêmes des consultations interprétées. Notre analyse des expériences des patients, des professionnels fournissant de soins de santé et des interprètes offre des preuves du besoin de dépasser le problème de langue. Et en faisant cela, nous adressons des multiples inégalités, souvent cachées dans des contextes de soins de santé, dans les milieux clinique et domicile. Nous proposons un programme de recherche basé sur la pratique, qui favorise la communication culturelle dans des milieux clinique et domicile, et qui reconnait le statut d’immigration comme un déterminant social de la santé

    First principles calculation of uniaxial magnetic anisotropy and magnetostriction in strained CMR films

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    We performed first - principles relativistic full-potential linearized augmented plane wave calculations for strained tetragonal ferromagnetic La(Ba)MnO3_3 with an assumed experimental structure of thin strained tetragonal La0.67_{0.67}Ca0.33_{0.33}MnO3_3 (LCMO) films grown on SrTiO3_3[001] and LaAlO3_3[001] substrates. The calculated uniaxial magnetic anisotropy energy (MAE) values, are in good quantitative agreement with experiment for LCMO films on SrTiO3_3 substrate. We also analyze the applicability of linear magnetoelastic theory for describing the stain dependence of MAE, and estimate magnetostriction coefficient λ001\lambda_{001}.Comment: Talk given at APS99 Meeting, Atlanta, 199

    Mistimed malaria parasites re‐synchronise with host feeding‐fasting rhythms by shortening the duration of intra‐erythrocytic development

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    AIMS: Malaria parasites exhibit daily rhythms in the intra‐erythrocytic development cycle (IDC) that underpins asexual replication in the blood. The IDC schedule is aligned with the timing of host feeding‐fasting rhythms. When the IDC schedule is perturbed to become mismatched to host rhythms, it readily reschedules but it is not known how. METHODS: We intensively follow four groups of infections that have different temporal alignments between host rhythms and the IDC schedule for 10 days, before and after the peak in asexual densities. We compare how the duration, synchrony and timing of the IDC differs between parasites in control infections and those forced to reschedule by 12 hours and ask whether the density of parasites affects the rescheduling process. RESULTS AND CONCLUSIONS: Our experiments reveal parasites shorten the IDC duration by 2–3 hours to become realigned to host feeding‐fasting rhythms with 5–6 days, in a density‐independent manner. Furthermore, parasites are able to reschedule without significant fitness costs for them or their hosts. Understanding the extent of, and limits on, plasticity in the IDC schedule may reveal targets for novel interventions, such as drugs to disrupt IDC regulation and preventing IDC dormancy conferring tolerance to existing drugs

    Distributed Drug Discovery, Part 2: Global Rehearsal of Alkylating Agents for the Synthesis of Resin-Bound Unnatural Amino Acids and Virtual D3 Catalog Construction

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    Re-circumscription of the mimosoid genus Entada including new combinations for all species of the phylogenetically nested Elephantorrhiza (Leguminosae, Caesalpinioideae, mimosoid clade)

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    Recent phylogenomic analyses of 997 nuclear genes support the long-held view that the genus Entada is congeneric with Elephantorrhiza. Entada is resolved as monophyletic only if the genus Elephantorrhiza is subsumed within it. The two genera were distinguished solely by relatively minor differences in the mode of dehiscence of the fruits (a craspedium separating into one-seeded endocarp segments in Entada versus a craspedium with the whole fruit valve breaking away from the persistent replum in Elephantorrhiza) and the craspedial fruit type itself provides a shared synapomorphy for the re-circumscribed Entada. Here, we provide a synopsis of Entada, including 11 new combinations in total, for the eight species, one subspecies and one variety previously placed in Elephantorrhiza, as well as a new combination for a subspecies of Entada rheedei Spreng. not previously dealt with when Entada pursaetha DC. was placed in synonymy. These new combinations are: Entada burkei (Benth.) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada elephantina (Burch.) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada goetzei (Harms) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada goetzei subsp. lata (Brenan & Brummitt) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada obliqua (Burtt Davy) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada praetermissa (J.H. Ross) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada rangei (Harms) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada rheedei subsp. sinohimalensis (Grierson & D.G. Long) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada schinziana (Dinter) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada woodii (E. Phillips) S.A. O’Donnell & G.P. Lewis, comb. nov.; and Entada woodii var. pubescens (E. Phillips) S.A. O’Donnell & G.P. Lewis, comb. nov. We provide a revised circumscription of the genus Entada which now comprises 40 species distributed pantropically, with the greatest diversity of species in tropical Africa. We present a complete taxonomic synopsis, including a map showing the global distribution of the genus and photographs showing variation amongst species in habit, foliage, flowers and fruits. A short discussion about extrafloral nectaries, mainly observed in the Madagascan species, is presented

    The 2-3 symmetry: Flavour Changing bb, τ\tau Decays and Neutrino Mixing

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    The observed pattern of neutrino mixing may be the result of a 2-3(μτ \mu- \tau) symmetry in the leptonic sector. We consider a two Higgs doublet model with a 2-3 symmetry in the down type quark and the charged lepton sector. The breaking of the 2-3 symmetry by the strange quark mass and the muon mass leads to FCNC in the quark sector and the charged lepton sector that are suppressed by msmb{m_s \over m_b} and mμmτ{m_{\mu} \over m_{\tau}} in addition to the mass of the heavy Higgs boson of the second Higgs doublet. A Higgs boson mass of mH600900 m_H \sim 600 - 900 GeV can explain the deviation from standard model reported in several rare B decays. Predictions for other B decays are made and a new CP phase is predicted in BsBˉsB_{s}-{\bar{B}_{s}} mixing. The lepton flavour violating decays τμlˉ(qˉ)l(q) \tau \to \mu \bar{l}(\bar{q}) l(q) are below the experimental limits. The breaking of 2-3 symmetry in the lepton sector can lead to deviations of the atmospheric neutrino mixing angle from the maximal value by 2 \sim 2 degrees.Comment: 21 pages, no figures. Reorganization and addition of text. Reference added and misprints corrected. Conclusions unchanged. Accepted for publicatio

    Charm and Bottom Semileptonic Decays

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    We review the present status of theoretical attempts to calculate the semileptonic charm and bottom decays and then present a calculation of these decays in the light--front frame at the kinematic point q2=0q^2=0. This allows us to evaluate the form factors at the same value of q2q^2, even though the allowed kinematic ranges for charm and bottom decays are very different. Also, at this kinematic point the decay is given in terms of only one form factor A0(0)A_{0}(0). For the ratio of the decay rates given by the E653 collaboration we show that the determination of the ratio of the Cabibbo--Kobayashi--Maskawa (CKM) matrix elements is consistent with that obtained from the unitarity constraint. At present, though, the unitarity method still has greater accuracy. Since comparisons of the semileptonic decays into ρ\rho and either electrons or muons will be available soon from the E791 Fermilab experiment, we also look at the massive muon case. We show that for a range of q2q^2 the SU(3)FSU(3)_F symmetry breaking is small even though the contributions of the various helicity amplitudes becomes more complicated. For BB decays, the decay BKˉB \rightarrow K^{*} \ell \bar{\ell} at q2=0q^2=0 involves an extra form factor coming from the photon contribution and so is not amenable to the same kind of analysis, leaving only the decay BKννˉB \rightarrow K^{*}\nu \bar{\nu} as a possibility. As the mass of the decaying particle increases we note that the SU(3)SU(3) symmetry becomes badly broken at q2=0q^2=0.Comment: Latex, 19 pages, two figures are attached, a minor change in the manuscript related to thi
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