Search results for "ASTER"

showing 10 items of 2223 documents

Frictional quantum decoherence

2007

The dynamics associated with a measurement-based master equation for quantum Brownian motion are investigated. A scheme for obtaining time evolution from general initial conditions is derived. This is applied to analyze dissipation and decoherence in the evolution of both a Gaussian and a Schr\"{o}dinger cat initial state. Dependence on the diffusive terms present in the master equation is discussed with reference to both the coordinate and momentum representations.

Statistics and ProbabilityPhysicsQuantum PhysicsQuantum decoherenceGaussianTime evolutionGeneral Physics and AstronomyFOS: Physical sciencesStatistical and Nonlinear PhysicsDissipationMomentumsymbols.namesakeClassical mechanicsModeling and SimulationMaster equationsymbolsQuantum Physics (quant-ph)QuantumMathematical PhysicsBrownian motion
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Time-dependent perturbation treatment of independent Raman schemes

2007

The problem of a trapped ion subjected to the action of two or more independent Raman schemes is analysed through a suitable time-dependent perturbative approach based on the factorization of the evolution operator in terms of other unitary operators. We show that the dynamics of the system may be traced back to an effective Hamiltonian up to a suitable dressing. Moreover, we give the method to write the master equation corresponding to the case wherein spontaneous decays occur.

Statistics and ProbabilityPhysicsSettore FIS/02 - Fisica Teorica Modelli E Metodi Matematicisuperposition (mathematics)modesGeneral Physics and AstronomyPerturbation (astronomy)Statistical and Nonlinear PhysicsUnitary stateSettore FIS/03 - Fisica Della MateriaIonsymbols.namesakeharmonic oscillatorOperator (computer programming)FactorizationModeling and SimulationQuantum mechanicsMaster equationsymbolsHamiltonian (quantum mechanics)Raman spectroscopyMathematical PhysicsJournal of Physics A: Mathematical and Theoretical
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Non-Hermitian Physics and Master Equations

2022

A longstanding tool to characterize the evolution of open Markovian quantum systems is the GKSL (Gorini-Kossakowski-Sudarshan-Lindblad) master equation. However, in some cases, open quantum systems can be effectively described with non-Hermitian Hamiltonians, which have attracted great interest in the last twenty years due to a number of unconventional properties, such as the appearance of exceptional points. Here, we present a short review of these two different approaches aiming in particular to highlight their relation and illustrate different ways of connecting non-Hermitian Hamiltonian to a GKSL master equation for the full density matrix.

Statistics and ProbabilityQuantum PhysicsNon-HermitianFOS: Physical sciencesStatistical and Nonlinear Physicsopen quantum systemsquantum opticsmaster equationsQuantum Physics (quant-ph)exceptional pointsSettore FIS/03 - Fisica Della MateriaMathematical PhysicsOpen Systems & Information Dynamics
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A tomographic approach to non-Markovian master equations

2010

We propose a procedure based on symplectic tomography for reconstructing the unknown parameters of a convolutionless non-Markovian Gaussian noisy evolution. Whenever the time-dependent master equation coefficients are given as a function of some unknown time-independent parameters, we show that these parameters can be reconstructed by means of a finite number of tomograms. Two different approaches towards reconstruction, integral and differential, are presented and applied to a benchmark model made of a harmonic oscillator coupled to a bosonic bath. For this model the number of tomograms needed to retrieve the unknown parameters is explicitly computed.

Statistics and ProbabilityQuantum PhysicsSettore FIS/02 - Fisica Teorica Modelli E Metodi MatematiciComputer scienceGaussianFOS: Physical sciencesGeneral Physics and AstronomyStatistical and Nonlinear PhysicsFunction (mathematics)symbols.namesakeTomography Gaussian evolutionModeling and SimulationMaster equationsymbolsApplied mathematicsTomographyDifferential (infinitesimal)Quantum Physics (quant-ph)Finite setMathematical PhysicsHarmonic oscillatorSymplectic geometry
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Structure Learning in Nested Effects Models

2007

Nested Effects Models (NEMs) are a class of graphical models introduced to analyze the results of gene perturbation screens. NEMs explore noisy subset relations between the high-dimensional outputs of phenotyping studies, e.g., the effects showing in gene expression profiles or as morphological features of the perturbed cell. In this paper we expand the statistical basis of NEMs in four directions. First, we derive a new formula for the likelihood function of a NEM, which generalizes previous results for binary data. Second, we prove model identifiability under mild assumptions. Third, we show that the new formulation of the likelihood allows efficiency in traversing model space. Fourth, we…

Statistics and ProbabilityTraverseComputer scienceMolecular Networks (q-bio.MN)Genes MHC Class IIPerturbation (astronomy)Genes InsectFeature selectionQuantitative Biology - Quantitative Methods03 medical and health sciences0302 clinical medicineGeneticsAnimalsheterocyclic compoundsQuantitative Biology - Molecular NetworksGraphical modelMolecular BiologyQuantitative Methods (q-bio.QM)Oligonucleotide Array Sequence Analysis030304 developmental biologyLikelihood Functions0303 health sciencesNanoelectromechanical systemsModels StatisticalModels GeneticGene Expression ProfilingGenomicsComputational MathematicsDrosophila melanogasterPhenotypeFOS: Biological sciencesBinary dataIdentifiabilityRNA InterferenceLikelihood functionAlgorithmAlgorithms030217 neurology & neurosurgery
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The Second APOKASC Catalog: The Empirical Approach

2018

We present a catalog of stellar properties for a large sample of 6676 evolved stars with APOGEE spectroscopic parameters and \textit{Kepler} asteroseismic data analyzed using five independent techniques. Our data includes evolutionary state, surface gravity, mean density, mass, radius, age, and the spectroscopic and asteroseismic measurements used to derive them. We employ a new empirical approach for combining asteroseismic measurements from different methods, calibrating the inferred stellar parameters, and estimating uncertainties. With high statistical significance, we find that asteroseismic parameters inferred from the different pipelines have systematic offsets that are not removed b…

Stellar populationoscillations (including pulsations) [stars]fundamental parameters [stars]KEPLERFOS: Physical sciencesAstrophysicsAstrophysics::Cosmology and Extragalactic Astrophysics01 natural sciences0103 physical sciencesOSCILLATIONSAstrophysics::Solar and Stellar AstrophysicsStatistical dispersionstars abundancesFIELD010303 astronomy & astrophysicsRed clumpScalingComputingMilieux_MISCELLANEOUSAstrophysics::Galaxy AstrophysicsSolar and Stellar Astrophysics (astro-ph.SR)PhysicsMIXING-LENGTH010308 nuclear & particles physicsAstronomy and AstrophysicsRadiusSurface gravityAGESRED GIANTSStarsStar clusterAstrophysics - Solar and Stellar AstrophysicsSpace and Planetary ScienceOPEN CLUSTERSAstrophysics::Earth and Planetary AstrophysicsBOLOMETRIC CORRECTIONS[PHYS.ASTR]Physics [physics]/Astrophysics [astro-ph]STARSASTEROSEISMIC MASS
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Synthesis and Characterization of Adducts Derived from the syn-Diastereomer of Benzo[a]pyrene 7,8-Dihydrodiol 9,10-Epoxide and the 5‘-d(CCTATAGATATCC…

1996

5'-d(CCTATAGATATCC) was reacted with each syn-enantiomer of trans-7,8-dihydroxy 9,10-epoxy 7,8,9,10-tetrahydrobenzo[a]pyrene (syn-BPDE). The (-)-enantiomer yielded one dominating adduct, whereas the (+)-enantiomer resulted in two major adducts. As indicated by optical spectroscopic methods, the major adduct derived from both (-)- and (+)-syn-BPDE involves cis addition of the C-10 position of the diol epoxide to the exocyclic amino group of deoxyguanosine [(-)-syn-BPDEc-N2-dG and (+)-syn-BPDEc-N2-dG, respectively], whereas the minor (+)-syn-BPDE adduct is identical to a trans adduct [(+)-syn-BPDEt-N2-dG]. The cis adducts as well as the (+)-syn-BPDEt-N2-dG adduct are chemically stable for sev…

Stereochemistry78-Dihydro-78-dihydroxybenzo(a)pyrene 910-oxideMolecular Sequence DataDiolOligonucleotidesEpoxideToxicologyAdductDNA Adductschemistry.chemical_compoundDrug StabilityDeoxyguanosineBase CompositionBase SequenceCircular DichroismTemperatureDiastereomerStereoisomerismGeneral MedicineFluorescenceSpectrometry Fluorescencenervous systemchemistryBenzo(a)pyreneNucleic Acid ConformationPyreneChemical Research in Toxicology
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Syntheses of Four Enantiomers of 2,3-Diendo- and 3-Endo-aminobicyclo[2.2.2]oct-5-ene-2-exo-carboxylic Acid and Their Saturated Analogues

2013

Abstract: Ethyl 2,3- diendo -3-aminobicyclo[2.2.2]oct- 5-ene-2-carboxylate ((±)- 1 ) was resolved with O , O '-dibenzoyltartaric acid via diastere omeric salt formation. The efficient synthesis of the enantiomers of 2,3- diendo -3-aminobicyclo[2.2.2]oct- 5-ene-2-carboxylic acid ((+)- 7 and (–)- 7 ), 3- endo -aminobicyclo[2.2.2]oct-5-ene-2- exo -carboxylic acid ((+)- 5 and (–)- 5 ), cis - and trans -3-aminobicyclo[2.2.2]octa ne-2-carboxylic acid ((+)- 6 , (–)- 6 , (+)- 8 and (–)- 8 ) was achieved via isomerization, hydrogenation and hydrolysis of the corresponding esters (–)- 1 and (+)- 1 . The stereochemistry and relative configurations of the synthesized compounds were determined by NMR sp…

StereochemistryCarboxylic acidCarboxylic AcidsPharmaceutical ScienceArticleAnalytical Chemistrylcsh:QD241-441Hydrolysislcsh:Organic chemistryDrug DiscoveryMoleculePhysical and Theoretical Chemistryta116Nuclear Magnetic Resonance BiomolecularEne reactionchemistry.chemical_classificationMolecular StructureChemistryOrganic ChemistryDiastereomerresolutionconstrained chiral β-amino acidsEstersNuclear magnetic resonance spectroscopycontinuous flow hydrogenationsChemistry (miscellaneous)bicyclic β-amino acid derivativesMolecular MedicineEnantiomercontinuous flow hydrogenations<b> </b>bicyclic beta-amino acid derivativesIsomerizationconstrained chiral beta-amino acids
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Individual stereoisomers of phosphinic dipeptide inhibitor of leucine aminopeptidase

2008

Abstract Individual stereoisomers of the phosphinic pseudodipeptide hPheψ[P(O)(OH)CH2]Phe were obtained by stereoselective liquid chromatographic separation as N- and C-terminally protected derivative on quinidine carbamate modified silica stationary phase. The stereoisomeric purity, exceeding 95% for each fraction, was determined before and after deprotection using two independent methods. The absolute configuration was rationally assigned by application of enantiomerically pure phosphinic acid substrates in the synthetic procedure and correlation with biological activity of the products. Substantial differences in inhibition of leucine aminopeptidase by the individual isomers revealed nov…

StereochemistryCarboxylic acidleucine aminopeptidaseClinical BiochemistryPharmaceutical ScienceBiochemistryChemical synthesisLeucyl Aminopeptidasechemistry.chemical_compoundinhibitorsDrug DiscoveryMolecular Biologychemistry.chemical_classificationDipeptideMolecular StructureChemistryOrganic Chemistryphosphinic dipeptidesDiastereomerAbsolute configurationStereoisomerismDipeptidesPhosphinic Acidsstereoselective separationMolecular MedicineStereoselectivityLeucineEnantiomerBioorganic &amp; Medicinal Chemistry Letters
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Triterpenoid saponins from the roots of Spergularia marginata.

2016

Phytochemical investigations of the roots of Spergularia marginata had led to the isolation of four previously undescribed triterpenoid saponins, a known one and one spinasterol glycoside. Their structures were established by extensive NMR and mass spectroscopic techniques as 3-O-β-D-glucuronopyranosyl echinocystic acid 28-O-α-L-arabinopyranosyl-(1 → 2)-α-L-rhamnopyranosyl-(1 → 3)-β-D-xylopyranosyl-(1 → 4)-α-L-rhamnopyranosyl-(1 → 2)-α-L- arabinopyranosyl ester, 3-O-β-D-glucopyranosyl-(1 → 3)-β-D-glucuronopyranosyl echinocystic acid 28-O-α-L-arabinopyranosyl-(1 → 2)-α-L-rhamnopyranosyl-(1 → 3)-β-D-xylopyranosyl-(1 → 4)-α-L-rhamnopyranosyl-(1 → 2)- α-L-arabinopyranosyl ester, 3-O-β-D-glucopy…

StereochemistryCaryophyllaceaeCaryophyllaceaePlant ScienceHorticulture01 natural sciencesBiochemistryPlant Rootschemistry.chemical_compoundTriterpenoidHumansOleanolic AcidCytotoxicityMolecular BiologyNuclear Magnetic Resonance Biomolecularchemistry.chemical_classificationbiologyMolecular Structure010405 organic chemistryGlycosideGeneral MedicineSaponinsbiology.organism_classificationTriterpenes0104 chemical sciences010404 medicinal & biomolecular chemistryMoroccoSpinasterolchemistryPhytochemicalTwo-dimensional nuclear magnetic resonance spectroscopySpergulariaPhytochemistry
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