A subtraction scheme for computing QCD jet cross sections at NNLO: regularization of real-virtual emission

We present a subtraction scheme for computing jet cross sections in electron-positron annihilation at next-to-next-to-leading order accuracy in perturbative QCD. In this second part we deal with the regularization of the real-virtual contribution to the NNLO correction.Comment: 32 pages, LaTeX file, uses pstrick

Antenna subtraction with hadronic initial states

The antenna subtraction method for the computation of higher order corrections to jet observables and exclusive cross sections at collider experiments is extended to include hadronic initial states. In addition to the already known antenna subtraction with both radiators in the final state (final-final antennae), we introduce antenna subtractions with one or two radiators in the initial state (initial-final or initial-initial antennae). For those, we derive the phase space factorization and discuss the allowed phase space mappings at NLO and NNLO. We present integrated forms for all antenna functions relevant to NLO calculations, and describe the construction of the full antenna subtraction terms at NLO on two examples. The extension of the formalism to NNLO is outlined.Comment: 33 pages, 3 figure

The infrared structure of e+ e- --> 3 jets at NNLO reloaded

This paper gives detailed information on the structure of the infrared singularities for the process e+ e- --> 3 jets at next-to-next-to-leading order in perturbation theory. Particular emphasis is put on singularities associated to soft gluons. The knowledge of the singularity structure allows the construction of appropriate subtraction terms, which in turn can be implemented into a numerical Monte Carlo program.Comment: 59 pages, additional comments added, version to be publishe

MEASURING WORKING HOURS INPUT IN VINE GROWING AT WORK ORGANIZATION BASED ON PHENOLOGICAL PHASES

Research was based on phenological phases of Italian Riesling, involving differences in labour and financial input for dry, optimal and wet weather. Worktime demand for certain operations in vine growing was determined with an analytic method, work day survey and We worked out alternatives for dry, optimum and wet weather on the basis of phenological phaseses. The worktime demand for the phenological phases with all their operations were analysed and planned in an itemized way based on our findings. We used them to work out the worktime demand for the given vine land for each operation. To analyse differences coming from diverse methods of cultivation and spacing, the material, operational and total costs of hand and mechanized labour were projected for 1 hectare and variance analysis was made

Calculation of electric quadrupole linestrengths for diatomic molecules: Application to the H2, CO, HF and O2 molecules

We present a unified variational treatment of the electric quadrupole (E2) matrix elements, Einstein coefficients, and line strengths for general open-shell diatomic molecules in the general purpose diatomic code \Duo. Transformation relations between the Cartesian representation (typically used in electronic structure calculations) to the tensorial representation (required for spectroscopic applications) of the electric quadrupole moment components are derived. The implementation has been validated against accurate theoretical calculations and experimental measurements of quadrupole intensities of 1H2 available in the literature. We also present accurate electronic structure calculations of the electric quadrupole moment functions for the X 1Σ+ electronic states of CO and HF at the CCSD(T) and MRCI levels of theory, respectively, as well for the a 1Δg - b 1Σg+ quadrupole transition moment of of O2 with MRCI level of theory. Accurate infrared E2 line lists for 12C16O and 1H19F are provided. A demonstration of spectroscopic applications is presented by simulating E2 spectra for 12C16O, 1H19F and 16O2 (Noxon a 1Δg - b 1Σg+ band)

Can variability in the effect of opioids on refractory breathlessness be explained by genetic factors?

© 2015, BMJ Publishing Group. All rights reserved. Objectives: Opioids modulate the perception of breathlessness with a considerable variation in response, with poor correlation between the required opioid dose and symptom severity. The objective of this hypothesis-generating, secondary analysis was to identify candidate single nucleotide polymorphisms (SNP) from those associated with opioid receptors, signalling or pain modulation to identify any related to intensity of breathlessness while on opioids. This can help to inform prospective studies and potentially lead to better tailoring of opioid therapy for refractory breathlessness. Setting: 17 hospice/palliative care services (tertiary services) in 11 European countries. Participants: 2294 people over 18 years of age on regular opioids for pain related to cancer or its treatment. Primary outcome measures: The relationship between morphine dose, breathlessness intensity (European Organisation for Research and Treatment of Cancer Core Quality of Life Questionnaire; EORTCQLQC30 question 8) and 112 candidate SNPs from 25 genes (n=588). Secondary outcome measures: The same measures for people on oxycodone (n=402) or fentanyl (n=429). Results: SNPs not in Hardy-Weinberg equilibrium or with allele frequencies ( < 5%) were removed. Univariate associations between each SNP and breathlessness intensity were determined with Benjamini-Hochberg false discovery rate set at 20%. Multivariable ordinal logistic regression, clustering over country and adjusting for available confounders, was conducted with remaining SNPs. For univariate morphine associations, 1 variant on the 5-hydroxytryptamine type 3B (HTR3B) gene, and 4 on the β-2-arrestin gene (ARRB2) were associated with more intense breathlessness. 1 SNP remained significant in the multivariable model: people with rs7103572 SNP (HTR3B gene; present in 8.4% of the population) were three times more likely to have more intense breathlessness (OR 2.86; 95% CIs 1.46 to 5.62; p=0.002). No associations were seen with fentanyl nor with oxycodone. Conclusions: This large, exploratory study identified 1 biologically plausible SNP that warrants further study in the response of breathlessness to morphine therapy

Subtraction at NNLO

We propose a framework for the implementation of a subtraction formalism at NNLO in QCD, based on an observable- and process-independent cancellation of infrared singularities. As a first simple application, we present the calculation of the contribution to the e+e- dijet cross section proportional to C_F T_RComment: 42 pages Latex; 7 figures included. Modifications to the text, and references added; the results are unchange

The fully differential hadronic production of a Higgs boson via bottom quark fusion at NNLO

The fully differential computation of the hadronic production cross section of a Higgs boson via bottom quarks is presented at NNLO in QCD. Several differential distributions with their corresponding scale uncertainties are presented for the 8 TeV LHC. This is the first application of the method of non-linear mappings for NNLO differential calculations at hadron colliders.Comment: 27 pages, 13 figures, 1 lego plo

Can variability in the effect of opioids on refractory breathlessness be explained by genetic factors?

© 2015, BMJ Publishing Group. All rights reserved. Objectives: Opioids modulate the perception of breathlessness with a considerable variation in response, with poor correlation between the required opioid dose and symptom severity. The objective of this hypothesis-generating, secondary analysis was to identify candidate single nucleotide polymorphisms (SNP) from those associated with opioid receptors, signalling or pain modulation to identify any related to intensity of breathlessness while on opioids. This can help to inform prospective studies and potentially lead to better tailoring of opioid therapy for refractory breathlessness. Setting: 17 hospice/palliative care services (tertiary services) in 11 European countries. Participants: 2294 people over 18 years of age on regular opioids for pain related to cancer or its treatment. Primary outcome measures: The relationship between morphine dose, breathlessness intensity (European Organisation for Research and Treatment of Cancer Core Quality of Life Questionnaire; EORTCQLQC30 question 8) and 112 candidate SNPs from 25 genes (n=588). Secondary outcome measures: The same measures for people on oxycodone (n=402) or fentanyl (n=429). Results: SNPs not in Hardy-Weinberg equilibrium or with allele frequencies (<5%) were removed. Univariate associations between each SNP and breathlessness intensity were determined with Benjamini-Hochberg false discovery rate set at 20%. Multivariable ordinal logistic regression, clustering over country and adjusting for available confounders, was conducted with remaining SNPs. For univariate morphine associations, 1 variant on the 5-hydroxytryptamine type 3B (HTR3B) gene, and 4 on the β-2-arrestin gene (ARRB2) were associated with more intense breathlessness. 1 SNP remained significant in the multivariable model: people with rs7103572 SNP (HTR3B gene; present in 8.4% of the population) were three times more likely to have more intense breathlessness (OR 2.86; 95% CIs 1.46 to 5.62; p=0.002). No associations were seen with fentanyl nor with oxycodone. Conclusions: This large, exploratory study identified 1 biologically plausible SNP that warrants further study in the response of breathlessness to morphine therapy