Search results for "branch"

showing 10 items of 1278 documents

Evidence for the decays of and *

2019

Abstract We study the hadronic decays of to the final states and , using an annihilation data sample of 567 pb-1 taken at a center-of-mass energy of 4.6 GeV with the BESIII detector at the BEPCII collider. We find evidence for the decays and with statistical significance of and , respectively. Normalizing to the reference decays and , we obtain the ratios of the branching fractions and to be and , respectively. The upper limits at the 90% confidence level are set to be and . Using BESIII measurements of the branching fractions of the reference decays, we determine % (<0.68%) and % (<1.9%). Here, the first uncertainties are statistical and the second systematic. The obtained branching …

Hadronic decayPhysicsNuclear and High Energy Physics010308 nuclear & particles physicsBranching fractionHadronAstronomy and AstrophysicsLambda01 natural sciencesOmegaCombinatorics0103 physical sciences010306 general physicsInstrumentationChinese Physics C
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Dalitz plot analysis ofD0→K¯0K+K−

2005

A Dalitz plot analysis of approximately 12500 D0 events reconstructed in the hadronic decay D0-->K0bar K+ K- is presented. This analysis is based on a data sample of 91.5 fb-1 collected with the BaBar detector at the PEP-II asymmetric-energy e+ e- storage rings at SLAC running at center-of-mass energies on and 40 MeV below the Y4S resonance. The events are selected from e+ e- --> c cbar annihilations using the decay D*+ --> D0 pi+. The following ratio of branching fractions has been obtained: BR = Gamma(D0-->K0bar K+ K-)/Gamma(D0-->K0bar pi+ pi-) = (15.8+/-0.1(stat.)+/-0.5(syst.)x 10-2 Estimates of fractions and phases for resonant and non-resonant contributions to the Dalitz plot are also …

Hadronic decayPhysicsNuclear and High Energy PhysicsAnnihilation010308 nuclear & particles physicsBranching fractionElectron–positron annihilationPartial wave analysisDalitz plot01 natural sciencesParticle identificationNuclear physics0103 physical sciences010306 general physicsPhysical Review D
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Search for the rare charmless hadronic decayB+→a0+π0

2008

We present a search for B decays to a charged scalar meson a0+ and a pi0 where the a0+ decays to an eta meson and a pi+. The analysis was performed on a data sample consisting of 383x10-6 BBbar pairs collected with the Babar detector at the PEP-II asymmetric-energy B Factory at SLAC. We find no significant signal and set an upper limit on the product branching fraction BF[(B+ -> a0+ pi0) x (a0+ -> eta pi+)] of 1.4x10-6 at the 90% confidence level.

Hadronic decayPhysicsNuclear and High Energy PhysicsParticle physics010308 nuclear & particles physicsBranching fractionElectron–positron annihilationEta meson01 natural sciencesParticle identificationB-factoryNuclear physics0103 physical sciencesHigh Energy Physics::ExperimentNuclear Experiment010306 general physicsScalar mesonPhysical Review D
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Model-independent search for the decay B^{+}→l^{+}ν_{l}γ

2009

We present a search for the radiative leptonic decay B^+ → l^+ν_lγ, where l = e, μ, using a data sample of 465 × 10^6 BB(overbar) pairs collected by the BABAR experiment. In this analysis, we fully reconstruct the hadronic decay of one of the B mesons in Υ(4S) → B^+B^- decays, then search for evidence of B^+ → l^+ν_lγ in the rest of the event. We observe no significant evidence of signal decays and report model-independent branching fraction upper limits of B(B^+ → e^+ν_eγ) < 17 × 10^(-6), B(B^+ → μ^+ν_μγ) < 24 × 10^(-6), and B(B^+ → l^+ν_lγ) < 15.6 × 10^(-6) (l= e or μ), all at the 90% confidence level.

Hadronic decayPhysicsNuclear and High Energy PhysicsParticle physicsMuon010308 nuclear & particles physicsBranching fractionElectron–positron annihilationRadiative decayBaBar experimentElectronAstrophysics01 natural sciences0103 physical sciencesB meson010306 general physics
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Measurement of the ratio ofBc+branching fractions toJ/ψπ+andJ/ψμ+νμfinal states

2014

The first measurement that relates semileptonic and hadronic decay rates of the B-c(+) meson is performed using proton-proton collision data corresponding to 1.0 fb(-1) of integrated luminosity collected with the LHCb detector. The measured value of the ratio of branching fractions, B(B-c(+) -> J/psi pi(+))/B(B-c(+) -> J/psi mu(+)nu(mu)) = 0.0469 +/- 0.0028(stat) +/- 0.0046(syst), is at the lower end of available theoretical predictions.

Hadronic decayPhysicsNuclear physicsSemileptonic decayNuclear and High Energy PhysicsMesonBranching fractionPiHeavy quark effective theoryHigh Energy Physics::ExperimentNuclear ExperimentBranching (polymer chemistry)Physical Review D
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Measurements of absolute hadronic branching fractions of the Λc+ baryon

2016

Kolcu, Onur Buğra (Arel Author) --- Makale 69 yazarlıdır.

Hadronic decayPhysicsParticle physicsBESIII детектор010308 nuclear & particles physicsBranching fractionElectron–positron annihilationадроныHigh Energy Physics::PhenomenologyHadronGeneral Physics and AstronomyBranching (polymer chemistry)Lambda01 natural sciencesNOdecayBaryonNuclear physicsPhysics and Astronomy (all)0103 physical sciencesбарионыHigh Energy Physics::Experiment010306 general physicsRadioactive decay
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Determination of the Ratio ofb-Quark Fragmentation Fractionsfs/fdinppCollisions ats=7  TeVwith the ATLAS Detector

2015

With an integrated luminosity of 2.47 fb^{-1} recorded by the ATLAS experiment at the LHC, the exclusive decays B_{s}^{0}→J/ψϕ and B_{d}^{0}→J/ψK^{*0} of B mesons produced in pp collisions at sqrt[s]=7 TeV are used to determine the ratio of fragmentation fractions f_{s}/f_{d}. From the observed B_{s}^{0}→J/ψϕ and B_{d}^{0}→J/ψK^{*0} yields, the quantity (f_{s}/f_{d})[B(B_{s}^{0}→J/ψϕ)/B(B_{d}^{0}→J/ψK^{*0})] is measured to be 0.199±0.004(stat)±0.008(syst). Using a recent theory prediction for [B(B_{s}^{0}→J/ψϕ)/B(B_{d}^{0}→J/ψK^{*0})] yields (f_{s}/f_{d})=0.240±0.004(stat)±0.010(syst)±0.017(th). This result is based on a new approach that provides a significant improvement of the world aver…

Hadronic decayPhysicsParticle physicsFragmentation (mass spectrometry)MesonAtlas detectorBranching fractionGeneral Physics and AstronomyB mesonAstrophysicsTellurium compoundsBottom quarkPhysical Review Letters
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Chronic toxicity of methylparathion to Daphnia magna: Effects on survival, reproduction, and growth

1995

Health Toxicology and Mutagenesismedia_common.quotation_subjectDaphnia magnaBranchiopodaZoologyMethyl ParathionToxicologyToxicologyToxicity TestsAnimalsEcotoxicologyChronic toxicitymedia_commonAnalysis of VariancebiologyReproductionGeneral Medicinebiology.organism_classificationPollutionInvestigation methodsDaphniaCladoceraToxicityFemalePest ControlReproductionWater Pollutants ChemicalBulletin of Environmental Contamination and Toxicology
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Data from: Phylogenomics of Lophotrochozoa with consideration of systematic error

2021

Phylogenomic studies have improved understanding of deep metazoan phylogeny and show promise for resolving incongruences among analyses based on limited numbers of loci. One region of the animal tree that has been especially difficult to resolve, even with phylogenomic approaches, is relationships within Lophotrochozoa (the animal clade that includes molluscs, annelids, and flatworms among others). Lack of resolution in phylogenomic analyses could be due to insufficient phylogenetic signal, limitations in taxon and/or gene sampling, or systematic error. Here, we investigated why lophotrochozoan phylogeny has been such a difficult question to answer by identifying and reducing sources of sys…

Helobdella robustaGlycera dibranchiataMytilus edulisAnnelidaEntalina tetragonaLeptochiton asellusCerebratulus marginatusLoxosomella cf. viviparaGraptacme eboreaLineus longissimusmedicine and health careClymenella torquataRuditapes philippinarumNucella lapillusHaliotis rufescenslong branch attractionPlatyzoaBarentsia gracilisPriapulus caudatusLineus ruberAlitta virenssaturationProchaetoderma californicumLife SciencesPinctada fucataSchistosoma mansoniPolyzoaCephalothrix hongkongensisRhyssoplax olivaceusLoxosoma pectinaricolaPhascolosoma agassiziiAdineta vagaDrosophila melanogasterEntoproctaBugula neritinaPhoronis vancouverensisMedicineNovocrania anomalaVillosa lienosaDaphnia pulexSagitta sp.Pectinaria gouldiiSymbion americanusNuculana pernulaSepia esculentaEnucula tenuisSolemya velumLineus lacteusTubulanus polymorphus-StruckGnathostomula paradoxaBoccardia proboscideaMacellomenia schanderiLaevipilina hyalinaTubulanus polymorphus-HalanychBryozoaPomatoceros lamarckiiSepioteuthis lessonianaParanemertes peregrinaMalacobdella grossaHemithiris psittaceaLeptochiton rugatusTrochozoaBrachionus plicatilisSpathoderma clenchiLaqueus californicusPatella vulgataLottia giganteaCrepidula fornicataPhoronidaAplysia californicaGlottidia pyramidataPhoronis psammophilaSchmidtea mediterraneaAlexandromenia crassaBrachiopodaMegadasys sp.Octopus vulgarisCapitella teletaNeomenia carinatacompositional heterogeneityNemerteaPhenacolepas pulchellaGadila tolmieiMolluscaMacrodasys sp.Crassostrea gigasPedicellina cernuaTaenia pisiformisDosidicus gigasCephalothrix linearisSpiralia
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Data from: Phylogenomics of Lophotrochozoa with consideration of systematic error

2016

Phylogenomic studies have improved understanding of deep metazoan phylogeny and show promise for resolving incongruences among analyses based on limited numbers of loci. One region of the animal tree that has been especially difficult to resolve, even with phylogenomic approaches, is relationships within Lophotrochozoa (the animal clade that includes molluscs, annelids, and flatworms among others). Lack of resolution in phylogenomic analyses could be due to insufficient phylogenetic signal, limitations in taxon and/or gene sampling, or systematic error. Here, we investigated why lophotrochozoan phylogeny has been such a difficult question to answer by identifying and reducing sources of sys…

Helobdella robustaGlycera dibranchiataMytilus edulisAnnelidaEntalina tetragonaLeptochiton asellusCerebratulus marginatusLoxosomella cf. viviparaGraptacme eboreaLineus longissimusmedicine and health careClymenella torquataRuditapes philippinarumNucella lapillusHaliotis rufescenslong branch attractionPlatyzoaBarentsia gracilisPriapulus caudatusLineus ruberAlitta virenssaturationProchaetoderma californicumPinctada fucataSchistosoma mansoniLife sciencesPolyzoaCephalothrix hongkongensisRhyssoplax olivaceusLoxosoma pectinaricolaPhascolosoma agassiziiAdineta vagaDrosophila melanogasterEntoproctaBugula neritinaPhoronis vancouverensisMedicineNovocrania anomalaVillosa lienosaDaphnia pulexSagitta sp.Pectinaria gouldiiSymbion americanusNuculana pernulaSepia esculentaEnucula tenuisSolemya velumLineus lacteusTubulanus polymorphus-StruckGnathostomula paradoxaBoccardia proboscideaMacellomenia schanderiLaevipilina hyalinaTubulanus polymorphus-HalanychBryozoaPomatoceros lamarckiiSepioteuthis lessonianaParanemertes peregrinaMalacobdella grossaHemithiris psittaceaLeptochiton rugatusTrochozoaBrachionus plicatilisSpathoderma clenchiLaqueus californicusPatella vulgataLottia giganteaCrepidula fornicataPhoronidaAplysia californicaGlottidia pyramidataPhoronis psammophilaSchmidtea mediterraneaAlexandromenia crassaBrachiopodaMegadasys sp.Octopus vulgarisCapitella teletaNeomenia carinatacompositional heterogeneityNemerteaPhenacolepas pulchellaGadila tolmieiMolluscaMacrodasys sp.Crassostrea gigasPedicellina cernuaTaenia pisiformisDosidicus gigasCephalothrix linearisSpiralia
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