33 research outputs found

    Three-dimensional parton distribution functions g1Tg_{1T} and h1Lh_{1L}^\perp in the polarized proton-antiproton Drell-Yan process

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    We present predictions of the unweighted and weighted double spin asymmetries related to the transversal helicity distribution g1Tg_{1T} and the longitudinal transversity distribution h1Lh_{1L}^\perp, two of eight leading-twist transverse momentum dependent parton distributions (TMDs) or three-dimensional parton distribution functions (3dPDFs), in the polarized proton-antiproton Drell-Yan process at typical kinematics on the Facility for Antiproton and Ion Research (FAIR). We conclude that FAIR is ideal to access the new 3dPDFs towards a detailed picture of the nucleon structure.Comment: 6 latex pages, 5 figures, version for publication in EPJ

    Azimuthal asymmetries in lepton-pair production at a fixed-target experiment using the LHC beams (AFTER)

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    A multi-purpose fixed-target experiment using the proton and lead-ion beams of the LHC was recently proposed by Brodsky, Fleuret, Hadjidakis and Lansberg, and here we concentrate our study on some issues related to the spin physics part of this project (referred to as AFTER). We study the nucleon spin structure through pppp and pdpd processes with a fixed-target experiment using the LHC proton beams, for the kinematical region with 7 TeV proton beams at the energy in center-of-mass frame of two nucleons s=115\sqrt{s}=115 GeV. We calculate and estimate the cos2ϕ\cos2\phi azimuthal asymmetries of unpolarized pppp and pdpd dilepton production processes in the Drell--Yan continuum region and at the ZZ-pole. We also calculate the sin(2ϕϕS)\sin(2\phi-\phi_S), sin(2ϕ+ϕS)\sin(2\phi+\phi_S) and sin2ϕ\sin2\phi azimuthal asymmetries of pppp and pdpd dilepton production processes with the target proton and deuteron longitudinally or transversally polarized in the Drell--Yan continuum region and around ZZ resonances region. We conclude that it is feasible to measure these azimuthal asymmetries, consequently the three-dimensional or transverse momentum dependent parton distribution functions (3dPDFs or TMDs), at this new AFTER facility.Comment: 15 pages, 40 figures. Version accepted for publication in EPJ

    Left-right asymmetry for pion and kaon production in the semi-inclusive deep inelastic scattering process

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    We analyze the left-right asymmetry in the semi-inclusive deep inelastic scattering (SIDIS) process without introducing any weighting functions. With the current theoretical understanding, we find that the Sivers effect plays a key role in our analysis. We use the latest parametrization of the Sivers and fragmentation functions to reanalyze the π±\pi^\pm production process and find that the results are sensitive to the parametrization. We also extend our calculation on the K±K^{\pm} production, which can help us know more about the Sivers distribution of the sea quarks and the unfavored fragmentation processes. HERMES kinematics with a proton target, COMPASS kinematics with a proton, deuteron, and neutron target (the information on the neutron target can be effectively extracted from the 3^3He target), and JLab kinematics (both 6 GeV and 12 GeV) with a proton and neutron target are considered in our paper.Comment: 7 latex pages, 11 figures, final version for publication, with references update

    Longitudinal Polarization of Lambda and anti-Lambda Hyperons in Lepton-Nucleon Deep-Inelastic Scattering

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    We consider models for the spin transfers to Λ\Lambda and Λˉ\bar{\Lambda} hyperons produced in lepton-nucleon deep-inelastic scattering. We make predictions for longitudinal Λ\Lambda and Λˉ\bar{\Lambda} spin transfers for the COMPASS experiment and for HERA, and for the spin transfer to Λ\Lambda hyperons produced at JLAB. We demonstrate that accurate measurements of the spin transfers to Λ\Lambda and Λˉ\bar{\Lambda} hyperons with COMPASS kinematics have the potential to probe the intrinsic strangeness in the nucleon. We show that a measurement of Λˉ\bar{\Lambda} polarisation could provide a clean probe of the spin transfer from sˉ\bar{s} quarks and provides a new possibility to measure the antistrange quark distribution function. COMPASS data in a domain of x that has not been studied previously will provide valuable extra information to fix models for the nucleon spin structure. The spin transfer to Λˉ\bar{\Lambda} hyperons, which could be measured by the COMPASS experiment, would provide a new tool to distinguish between the SU(6) and Burkardt-Jaffe (BJ) models for baryon spin structure. In the case of the HERA electron-proton collider experiments with longitudinally-polarised electrons, the separation between the target and current fragmentation mechanisms is more clear. It provides a complementary probe of the strange quark distribution and helps distinguish between the SU(6) and BJ models for the Λ\Lambda and Λˉ\bar{\Lambda} spin structure. Finally, we show that the spin transfer to Λ\Lambda hyperons measured in a JLAB experiment would be dominated by the spin transfer of the intrinsic polarised-strangeness in the remnant nucleon, providing an independent way to check our model predictions.Comment: minor changes after accepted to EPJ

    Observation of the astrophysically important 3+ state in 18Ne via elastic scattering of a radioactive 17F beam from 1H

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    The 17F(p, γ)18 reaction is important in stellar explosions, but its rate has been uncertain because of an expected 3+ state in 18Ne that has never been conclusively observed. This state would provide a strong l = 0 resonance and, depending on its excitation energy, could dominate the stellar reaction rate. We have observed this missing 3+ state by measuring the 1H(17F, p)17F excitation function with a radioactive 17F beam at the ORNL Holifield Radioactive Ion Beam Facility. We find that the state lies at a center-of-mass energy of Er = 599.8 ± 1.5stat ± 2.0sys keV (Ex = 4523.7 ± 2.9keV) and has a width of Γ = 18 ± 2stat ± 1sys keV

    The astrophysically important 3+ state in 18Ne and the 17F(py)18Ne stellar rate

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    Knowledge of the [Formula Presented] reaction rate is important for understanding stellar explosions, but it was uncertain because the properties of an expected but previously unobserved [Formula Presented] state in [Formula Presented] were not known. This state would provide a strong s-wave resonance for the [Formula Presented] system and, depending on its excitation energy, could dominate the stellar reaction rate at temperatures above 0.2 GK. We have observed this missing [Formula Presented] state by measuring the [Formula Presented] excitation function with a radioactive [Formula Presented] beam at the ORNL Holifield Radioactive Ion Beam Facility (HRIBF). We find that the state lies at a center-of-mass energy of [Formula Presented] keV [Formula Presented] and has a width of [Formula Presented] The measured properties of the resonance are only consistent with a [Formula Presented] assignment

    Magnetic order in spin-1 and spin-3/2 interpolating square-triangle Heisenberg antiferromagnets

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    Using the coupled cluster method we investigate spin-ss J1J_{1}-J2J_{2}' Heisenberg antiferromagnets (HAFs) on an infinite, anisotropic, triangular lattice when the spin quantum number s=1s=1 or s=3/2s=3/2. With respect to a square-lattice geometry the model has antiferromagnetic (J1>0J_{1} > 0) bonds between nearest neighbours and competing (J2>0J_{2}' > 0) bonds between next-nearest neighbours across only one of the diagonals of each square plaquette, the same one in each square. In a topologically equivalent triangular-lattice geometry, we have two types of nearest-neighbour bonds: namely the J2κJ1J_{2}' \equiv \kappa J_{1} bonds along parallel chains and the J1J_{1} bonds producing an interchain coupling. The model thus interpolates between an isotropic HAF on the square lattice at κ=0\kappa = 0 and a set of decoupled chains at κ\kappa \rightarrow \infty, with the isotropic HAF on the triangular lattice in between at κ=1\kappa = 1. For both the s=1s=1 and the s=3/2s=3/2 models we find a second-order quantum phase transition at κc=0.615±0.010\kappa_{c}=0.615 \pm 0.010 and κc=0.575±0.005\kappa_{c}=0.575 \pm 0.005 respectively, between a N\'{e}el antiferromagnetic state and a helical state. In both cases the ground-state energy EE and its first derivative dE/dκdE/d\kappa are continuous at κ=κc\kappa=\kappa_{c}, while the order parameter for the transition (viz., the average on-site magnetization) does not go to zero on either side of the transition. The transition at κ=κc\kappa = \kappa_{c} for both the s=1s=1 and s=3/2s=3/2 cases is analogous to that observed in our previous work for the s=1/2s=1/2 case at a value κc=0.80±0.01\kappa_{c}=0.80 \pm 0.01. However, for the higher spin values the transition is of continuous (second-order) type, as in the classical case, whereas for the s=1/2s=1/2 case it appears to be weakly first-order in nature (although a second-order transition could not be excluded).Comment: 17 pages, 8 figues (Figs. 2-7 have subfigs. (a)-(d)

    Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950–2019: a comprehensive demographic analysis for the Global Burden of Disease Study 2019

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    Background: Accurate and up-to-date assessment of demographic metrics is crucial for understanding a wide range of social, economic, and public health issues that affect populations worldwide. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 produced updated and comprehensive demographic assessments of the key indicators of fertility, mortality, migration, and population for 204 countries and territories and selected subnational locations from 1950 to 2019. Methods: 8078 country-years of vital registration and sample registration data, 938 surveys, 349 censuses, and 238 other sources were identified and used to estimate age-specific fertility. Spatiotemporal Gaussian process regression (ST-GPR) was used to generate age-specific fertility rates for 5-year age groups between ages 15 and 49 years. With extensions to age groups 10–14 and 50–54 years, the total fertility rate (TFR) was then aggregated using the estimated age-specific fertility between ages 10 and 54 years. 7417 sources were used for under-5 mortality estimation and 7355 for adult mortality. ST-GPR was used to synthesise data sources after correction for known biases. Adult mortality was measured as the probability of death between ages 15 and 60 years based on vital registration, sample registration, and sibling histories, and was also estimated using ST-GPR. HIV-free life tables were then estimated using estimates of under-5 and adult mortality rates using a relational model life table system created for GBD, which closely tracks observed age-specific mortality rates from complete vital registration when available. Independent estimates of HIV-specific mortality generated by an epidemiological analysis of HIV prevalence surveys and antenatal clinic serosurveillance and other sources were incorporated into the estimates in countries with large epidemics. Annual and single-year age estimates of net migration and population for each country and territory were generated using a Bayesian hierarchical cohort component model that analysed estimated age-specific fertility and mortality rates along with 1250 censuses and 747 population registry years. We classified location-years into seven categories on the basis of the natural rate of increase in population (calculated by subtracting the crude death rate from the crude birth rate) and the net migration rate. We computed healthy life expectancy (HALE) using years lived with disability (YLDs) per capita, life tables, and standard demographic methods. Uncertainty was propagated throughout the demographic estimation process, including fertility, mortality, and population, with 1000 draw-level estimates produced for each metric. Findings: The global TFR decreased from 2•72 (95% uncertainty interval [UI] 2•66–2•79) in 2000 to 2•31 (2•17–2•46) in 2019. Global annual livebirths increased from 134•5 million (131•5–137•8) in 2000 to a peak of 139•6 million (133•0–146•9) in 2016. Global livebirths then declined to 135•3 million (127•2–144•1) in 2019. Of the 204 countries and territories included in this study, in 2019, 102 had a TFR lower than 2•1, which is considered a good approximation of replacement-level fertility. All countries in sub-Saharan Africa had TFRs above replacement level in 2019 and accounted for 27•1% (95% UI 26•4–27•8) of global livebirths. Global life expectancy at birth increased from 67•2 years (95% UI 66•8–67•6) in 2000 to 73•5 years (72•8–74•3) in 2019. The total number of deaths increased from 50•7 million (49•5–51•9) in 2000 to 56•5 million (53•7–59•2) in 2019. Under-5 deaths declined from 9•6 million (9•1–10•3) in 2000 to 5•0 million (4•3–6•0) in 2019. Global population increased by 25•7%, from 6•2 billion (6•0–6•3) in 2000 to 7•7 billion (7•5–8•0) in 2019. In 2019, 34 countries had negative natural rates of increase; in 17 of these, the population declined because immigration was not sufficient to counteract the negative rate of decline. Globally, HALE increased from 58•6 years (56•1–60•8) in 2000 to 63•5 years (60•8–66•1) in 2019. HALE increased in 202 of 204 countries and territories between 2000 and 2019. Interpretation: Over the past 20 years, fertility rates have been dropping steadily and life expectancy has been increasing, with few exceptions. Much of this change follows historical patterns linking social and economic determinants, such as those captured by the GBD Socio-demographic Index, with demographic outcomes. More recently, several countries have experienced a combination of low fertility and stagnating improvement in mortality rates, pushing more populations into the late stages of the demographic transition. Tracking demographic change and the emergence of new patterns will be essential for global health monitoring. Funding: Bill & Melinda Gates Foundation. © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 licens

    Global burden of 87 risk factors in 204 countries and territories, 1990�2019: a systematic analysis for the Global Burden of Disease Study 2019

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    Background: Rigorous analysis of levels and trends in exposure to leading risk factors and quantification of their effect on human health are important to identify where public health is making progress and in which cases current efforts are inadequate. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 provides a standardised and comprehensive assessment of the magnitude of risk factor exposure, relative risk, and attributable burden of disease. Methods: GBD 2019 estimated attributable mortality, years of life lost (YLLs), years of life lived with disability (YLDs), and disability-adjusted life-years (DALYs) for 87 risk factors and combinations of risk factors, at the global level, regionally, and for 204 countries and territories. GBD uses a hierarchical list of risk factors so that specific risk factors (eg, sodium intake), and related aggregates (eg, diet quality), are both evaluated. This method has six analytical steps. (1) We included 560 risk�outcome pairs that met criteria for convincing or probable evidence on the basis of research studies. 12 risk�outcome pairs included in GBD 2017 no longer met inclusion criteria and 47 risk�outcome pairs for risks already included in GBD 2017 were added based on new evidence. (2) Relative risks were estimated as a function of exposure based on published systematic reviews, 81 systematic reviews done for GBD 2019, and meta-regression. (3) Levels of exposure in each age-sex-location-year included in the study were estimated based on all available data sources using spatiotemporal Gaussian process regression, DisMod-MR 2.1, a Bayesian meta-regression method, or alternative methods. (4) We determined, from published trials or cohort studies, the level of exposure associated with minimum risk, called the theoretical minimum risk exposure level. (5) Attributable deaths, YLLs, YLDs, and DALYs were computed by multiplying population attributable fractions (PAFs) by the relevant outcome quantity for each age-sex-location-year. (6) PAFs and attributable burden for combinations of risk factors were estimated taking into account mediation of different risk factors through other risk factors. Across all six analytical steps, 30 652 distinct data sources were used in the analysis. Uncertainty in each step of the analysis was propagated into the final estimates of attributable burden. Exposure levels for dichotomous, polytomous, and continuous risk factors were summarised with use of the summary exposure value to facilitate comparisons over time, across location, and across risks. Because the entire time series from 1990 to 2019 has been re-estimated with use of consistent data and methods, these results supersede previously published GBD estimates of attributable burden. Findings: The largest declines in risk exposure from 2010 to 2019 were among a set of risks that are strongly linked to social and economic development, including household air pollution; unsafe water, sanitation, and handwashing; and child growth failure. Global declines also occurred for tobacco smoking and lead exposure. The largest increases in risk exposure were for ambient particulate matter pollution, drug use, high fasting plasma glucose, and high body-mass index. In 2019, the leading Level 2 risk factor globally for attributable deaths was high systolic blood pressure, which accounted for 10·8 million (95 uncertainty interval UI 9·51�12·1) deaths (19·2% 16·9�21·3 of all deaths in 2019), followed by tobacco (smoked, second-hand, and chewing), which accounted for 8·71 million (8·12�9·31) deaths (15·4% 14·6�16·2 of all deaths in 2019). The leading Level 2 risk factor for attributable DALYs globally in 2019 was child and maternal malnutrition, which largely affects health in the youngest age groups and accounted for 295 million (253�350) DALYs (11·6% 10·3�13·1 of all global DALYs that year). The risk factor burden varied considerably in 2019 between age groups and locations. Among children aged 0�9 years, the three leading detailed risk factors for attributable DALYs were all related to malnutrition. Iron deficiency was the leading risk factor for those aged 10�24 years, alcohol use for those aged 25�49 years, and high systolic blood pressure for those aged 50�74 years and 75 years and older. Interpretation: Overall, the record for reducing exposure to harmful risks over the past three decades is poor. Success with reducing smoking and lead exposure through regulatory policy might point the way for a stronger role for public policy on other risks in addition to continued efforts to provide information on risk factor harm to the general public. Funding: Bill & Melinda Gates Foundation. © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 licens
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