53 research outputs found
Analytic Perturbation Theory: A New Approach to the Analytic Continuation of the Strong Coupling Constant into the Timelike Region
The renormalization group applied to perturbation theory is ordinarily used
to define the running coupling constant in the spacelike region. However, to
describe processes with timelike momenta transfers, it is important to have a
self-consistent determination of the running coupling constant in the timelike
region. The technique called analytic perturbation theory (APT) allows a
consistent determination of this running coupling constant. The results are
found to disagree significantly with those obtained in the standard
perturbative approach. Comparison between the standard approach and APT is
carried out to two loops, and threshold matching in APT is applied in the
timelike region.Comment: 16 pages, REVTeX, 7 postscript figure
Quantum Interaction : the Construction of Quantum Field defined as a Bilinear Form
We construct the solution of the quantum wave equation
as a bilinear form which can
be expanded over Wick polynomials of the free -field, and where
is defined as the normal ordered product with
respect to the free -field. The constructed solution is correctly defined
as a bilinear form on , where is a
dense linear subspace in the Fock space of the free -field. On
the diagonal Wick symbol of this bilinear form
satisfies the nonlinear classical wave equation.Comment: 32 pages, LaTe
The Determination of alpha_s from Tau Decays Revisited
We revisit the determination of alpha_s(m_tau) using a fit to inclusive tau
hadronic spectral moments in light of (1) the recent calculation of the
fourth-order perturbative coefficient K_4 in the expansion of the Adler
function, (2) new precision measurements from BABAR of e+e- annihilation cross
sections, which decrease the uncertainty in the separation of vector and
axial-vector spectral functions, and (3) improved results from BABAR and Belle
on tau branching fractions involving kaons. We estimate that the fourth-order
perturbative prediction reduces the theoretical uncertainty, introduced by the
truncation of the series, by 20% with respect to earlier determinations. We
discuss to some detail the perturbative prediction and show that the effect of
the incomplete knowledge of the series is reduced by using the so-called
contour-improved calculation, as opposed to fixed-order perturbation theory
which manifests convergence problems. The corresponding theoretical
uncertainties are studied at the tau and Z mass scales. Nonperturbative
contributions extracted from the most inclusive fit are small, in agreement
with earlier determinations. Systematic effects from quark-hadron duality
violation are estimated with simple models and found to be within the quoted
systematic errors. The fit gives alpha_s(m_tau) = 0.344 +- 0.005 +- 0.007,
where the first error is experimental and the second theoretical. After
evolution to M_Z we obtain alpha_s(M_Z) = 0.1212 +- 0.0005 +- 0.0008 +- 0.0005,
where the errors are respectively experimental, theoretical and due to the
evolution. The result is in agreement with the corresponding NNNLO value
derived from essentially the Z width in the global electroweak fit. The
alpha_s(M_Z) determination from tau decays is the most precise one to date.Comment: 22 pages, 7 figure
Fear expression is suppressed by tyrosine administration
Animal studies have demonstrated that catecholamines regulate several aspects of fear conditioning. In humans, however, pharmacological manipulations of the catecholaminergic system have been scarce, and their primary focus has been to interfering with catecholaminergic activity after fear acquisition or expression had taken place, using L-Dopa, primarily, as catecholaminergic precursor. Here, we sought to determine if putative increases in presynaptic dopamine and norepinephrine by tyrosine administered before conditioning could affect fear expression. Electrodermal activity (EDA) of 46 healthy participants (24 placebo, 22 tyrosine) was measured in a fear instructed task. Results showed that tyrosine abolished fear expression compared to placebo. Importantly, tyrosine did not affect EDA responses to the aversive stimulus (UCS) or alter participants' mood. Therefore, the effect of tyrosine on fear expression cannot be attributed to these factors. Taken together, these findings provide evidence that the catecholaminergic system influences fear expression in humans
A dopaminergic switch for fear to safety transitions
Overcoming aversive emotional memories requires neural systems that detect when fear responses are no longer appropriate. The midbrain ventral tegmental area (VTA) dopamine system has been implicated in reward and more broadly in signalling when a better than expected outcome has occurred. This suggests that it may be important in guiding fear to safety transitions. We report that when an expected aversive outcome does not occur, activity in midbrain dopamine neurons is necessary to extinguish behavioral fear responses and engage molecular signalling events in extinction learning circuits. Furthermore, a specific dopamine projection to the nucleus accumbens medial shell is partially responsible for this effect. By contrast, a separate dopamine projection to the medial prefrontal cortex opposes extinction learning. This demonstrates a novel function for the canonical VTA-dopamine reward system and reveals opposing behavioural roles for different dopamine neuron projections in fear extinction learning
A review on experimental and clinical genetic associations studies on fear conditioning, extinction and cognitive-behavioral treatment
Fear conditioning and extinction represent basic forms of associative learning with considerable clinical relevance and have been implicated in the pathogenesis of anxiety disorders. There is considerable inter-individual variation in the ability to acquire and extinguish conditioned fear reactions and the study of genetic variants has recently become a focus of research. In this review, we give an overview of the existing genetic association studies on human fear conditioning and extinction in healthy individuals and of related studies on cognitive-behavioral treatment (CBT) and exposure, as well as pathology development after trauma. Variation in the serotonin transporter (5HTT) and the catechol-o-methyltransferase (COMT) genes has consistently been associated with effects in pre-clinical and clinical studies. Interesting new findings, which however require further replication, have been reported for genetic variation in the dopamine transporter (DAT1) and the pituitary adenylate cyclase 1 receptor (ADCYAP1R1) genes, whereas the current picture is inconsistent for variation in the brain-derived neurotrophic factor (BDNF) gene. We end with a discussion of the findings and their limitations, as well as future directions that we hope will aid the field to develop further
Reply to Nielsen et al. social mindfulness is associated with countries’ environmental performance and individual environmental concern
info:eu-repo/semantics/publishedVersio
From local social mindfulness to global sustainability efforts?
info:eu-repo/semantics/publishedVersio
Perturbative QCD Calculations of Total Cross Sections and Decay Widths in Hard Inclusive Processes
A summary of the current understanding of methods of analytical higher order
perturbative computations of total cross sections and decay widths in Quantum
Chromodynamics is presented. As examples, the total cross section in electron
positron annihilation, the hadronic decay rates of the tau lepton and Higgs
boson up to O(\alpha_s^2) and O(\alpha_s^3) are considered. The evaluation of
the four-loop QED \beta - function at an intermediate step of the calculation
is briefly described. The problem of renormalization group ambiguity of
perturbative results is considered and some of the existing prescriptions are
discussed. The problem of estimation of theoretical uncertainty in perturbative
calculations is briefly discussed.Comment: 83 pages, LaTeX, Reviews of Modern Physics style, 14 figures plus
figural equations (not included). Hard copy available upon request at
[email protected]. To be published in Reviews of Modern Physic
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