491 research outputs found
The problem of equilibration and the computation of correlation functions on a quantum computer
We address the question of how a quantum computer can be used to simulate
experiments on quantum systems in thermal equilibrium. We present two
approaches for the preparation of the equilibrium state on a quantum computer.
For both approaches, we show that the output state of the algorithm, after long
enough time, is the desired equilibrium. We present a numerical analysis of one
of these approaches for small systems. We show how equilibrium
(time)-correlation functions can be efficiently estimated on a quantum
computer, given a preparation of the equilibrium state. The quantum algorithms
that we present are hard to simulate on a classical computer. This indicates
that they could provide an exponential speedup over what can be achieved with a
classical device.Comment: 25 pages LaTex + 8 figures; various additional comments, results and
correction
Determination of the Form Factors for the Decay B0 --> D*-l+nu_l and of the CKM Matrix Element |Vcb|
We present a combined measurement of the Cabibbo-Kobayashi-Maskawa matrix element and of the parameters , , and , which fully characterize the form factors of the decay in the framework of HQET, based on a sample of about 52,800 decays recorded by the BABAR detector. The kinematical information of the fully reconstructed decay is used to extract the following values for the parameters (where the first errors are statistical and the second systematic): , , , . By combining these measurements with the previous BABAR measurements of the form factors which employs a different technique on a partial sample of the data, we improve the statistical accuracy of the measurement, obtaining: and Using the lattice calculations for the axial form factor , we extract , where the third error is due to the uncertainty in
Study of the Exclusive Initial-State Radiation Production of the System
A study of exclusive production of the system through initial-state r adiation is performed in a search for charmonium states, where or . The mesons are reconstructed in the , , and decay modes. The is reconstructed through the decay mode. The analysis makes use of an integrated luminosity of 288.5 fb collected by the BaBar experiment. The mass spectrum shows a clear signal. Further structures appear in the 3.9 and 4.1 GeV/ regions. No evidence is found for Y(4260) decays to , implying an up per limit \frac{\BR(Y(4260)\to D \bar D)}{\BR(Y(4260)\to J/\psi \pi^+ \pi^-)} < 7.6 (95 % confidence level)
Measurement of the CP-Violating Asymmetry Amplitude sin2
We present results on time-dependent CP-violating asymmetries in neutral B decays to several CP eigenstates. The measurements use a data sample of about 88 million Y(4S) --> B Bbar decays collected between 1999 and 2002 with the BABAR detector at the PEP-II asymmetric-energy B Factory at SLAC. We study events in which one neutral B meson is fully reconstructed in a final state containing a charmonium meson and the other B meson is determined to be either a B0 or B0bar from its decay products. The amplitude of the CP-violating asymmetry, which in the Standard Model is proportional to sin2beta, is derived from the decay-time distributions in such events. We measure sin2beta = 0.741 +/- 0.067 (stat) +/- 0.033 (syst) and |lambda| = 0.948 +/- 0.051 (stat) +/- 0.017 (syst). The magnitude of lambda is consistent with unity, in agreement with the Standard Model expectation of no direct CP violation in these modes
Tear production, intraocular pressure and conjunctival microbiota, cytology and histology of New Zealand rabbits (Oryctolagus cuniculus)
The purpose of this study was to establish reference values for selected ophthalmic diagnostic tests in New Zealand rabbits (Oryctolagus cuniculus). A total of 22 adult male rabbits were used. The ophthalmic tests included evaluation of tear production with Schirmer tear test 1(STT1) and Endodontic absorbent paper point tear test (EAPPTT) using two different commercial brand materials. Applanation tonometry, Culture of the conjunctival bacterial flora, , conjunctival cytology and conjunctival histology were also performed. Mean (±SD) for STT1, EAPPTTa, EAPPTTb and IOP was 7.27±2.51mm/min, 12.43±1.69mm/min, 15.24±2.07mm/min, 12.89±2.80mm Hg, respectively. Staphylococcus epidermidis, Staphylococcus sp. and Bacillus sp. were predominant. The cytological evaluation revealed the presence columnar epithelial cells, superficial squamous keratinized cells, lymphocytes, heterophils, red blood cells, mucus and bacteria. The histological analysis revealed a stratified epithelium, characterized by the presence of columnar epithelial cells with a large number of goblet cells. The reported data can be used for therapeutic or experimental purposes
Relations between Financing and Output in the Not-for-Profit Hospital
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/68639/2/10.1177_107755878804500204.pd
Leaf anatomy of Qualea parviflora (Vochysiaceae) in three phytophysiognomies of the Mato Grosso State, Brazil
Thresholds of significant harm at global level: The journey of the Earth Commission
The planetary boundary framework proposes ‘safe’ boundaries, but these boundaries are not necessarily ‘just’. Hence, we ask: How has the Earth Commission defined just boundaries building on the concept of minimizing significant harm and how many people are currently exposed to harm above the safe and just threshold? We document the work of the Earth Commission to address these questions using our Earth System Justice framework. We conclude that: (a) from a justice perspective, nine criteria need to be considered when defining just boundaries; (b) the proportions of populations exposed to harm from exceeding safe and just boundaries today range from 11 to 84 % for the five domains studied (climate, biosphere, water, nutrients, aerosols); and (c) argue that the absolute upper limit for significant harm is possibly harm to 1 % of the population, which although not stringent enough to leave no one behind, would require radical transformations, given the populations currently already above the threshold
A comparative analysis of foliar chemical composition and leaf construction costs of beech (Fagus sylvatica L.), sycamore maple (Acer pseudoplatanus L.) and ash (Fraxinus excelsior L.) saplings along a light gradient
• Construction cost (g glucose g−1), chemical composition and morphology of
leaves of beech (Fagus sylvatica L.) and two co-occurring valuable
broadleaved species (sycamore maple – Acer pseudoplatanus L. – and ash –
Fraxinus excelsior L.) were investigated along a horizontal light
gradient (3–60% of above canopy radiation) and from top to bottom within the crowns in a
fairly even-aged mixed-species thicket established by natural regeneration beneath a
patchy shelterwood canopy.
• Construction cost and carbon concentration increased with irradiance in ash and
sycamore maple and were independent of irradiance in beech. Leaf traits expressed on an
area basis, like construction cost, nitrogen content and leaf mass (LMA) increased
significantly with irradiance in all three species and decreased from top to bottom within
crowns.
• The shade tolerant beech invested more glucose to produce a unit foliar biomass, but
less to build a unit foliar area due to lower LMA. Thereby beech was able to display a
greater total leaf area, what at least in parts counterbalanced the lower values of
Na as compared to ash and sycamore maple
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