Systematics of q anti-q states in the (n,M^2) and (J,M^2) planes

In the mass region up to M < 2400 MeV we systematise mesons on the plots (n,M^2) and (J,M^2), thus setting their classification in terms of n^{2S+1}L_J q anti-q states. The trajectories on the (n,M^2)-plots are drawn for the following (IJ^{PC})-states: a_0(10^{++}), a_1(11^{++}), a_2(12^{++}), a_3(13^{++}), a_4(14^{++}), pi(10^{-+}), pi_2(12^{-+}), eta(00^{-+}), eta_2(02^{-+})$, rho(11^{--}), f_0(00^{++}), f_2(02^{++}). All trajectories are linear, with nearly the same slopes. At the (J,M^2)-plot we set out meson states for leading and daughter trajectories: for pi, rho, a_1, a_2 and P'.Comment: 6 pages, LaTeX, 16 EPS figures, epsfig.st

Systematization of tensor mesons and the determination of the 2++2^{++} glueball

It is shown that new data on the $(J^{PC}=2^{++})$-resonances in the mass range $M\sim1700-2400$MeV support the linearity of the $(n,M^2)$-trajectories, where $n$ is the radial quantum number of quark--antiquark state. In this way all vacancies for the isoscalar tensor $q\bar q$-mesons in the range up to 2450 MeV are filled in. This allows one to fix the broad $f_2$-state with $M=2000\pm30$MeV and $\Gamma=530\pm40$MeV as the lowest tensor glueball. PACS numbers: 14.40.-n, 12.38.-t, 12.39.-MkComment: 10 pages, 1 figur

Formation of the internal structure of solids under severe action

On the example of a particular problem, the theory of vacancies, a new form of kinetic equations symmetrically incorporation the internal and free energies has been derived. The dynamical nature of irreversible phenomena at formation and motion of defects (dislocations) has been analyzed by a computer experiment. The obtained particular results are extended into a thermodynamic identity involving the law of conservation of energy at interaction with an environment (the 1st law of thermodynamics) and the law of energy transformation into internal degree of freedom (relaxation). The identity is compared with the analogous Jarzynski identity. The approach is illustrated by simulation of processes during severe plastic deformation, the Rybin kinetic equation for this case has been derived.Comment: 9 pages, 5 figure

Meson-meson scattering within one loop Chiral Perturbation Theory and its unitarization

We present the complete one-loop calculation of all the two meson scattering amplitudes within the framework of SU(3) Chiral Perturbation Theory, which includes pions, kaons and the eta. In addition, we have unitarized these amplitudes with the coupled channel Inverse Amplitude Method, which ensures simultaneously the good low energy properties of Chiral Perturbation Theory and unitarity. We show how this method provides a remarkable description of meson-meson scattering data up to 1.2 GeV including the scattering lengths and the generation of seven light resonances, which is consistent with previous determination of the chiral parameters. Particular attention is paid to discuss the differences and similarities of this work with previous analysis in the literature.Comment: 20 pages, 5 figures. Comments on sigma, kappa and eta', as well as some references added. Final version to appear in Phys.Rev.

Non-Equilibrium Evolution Thermodynamics Theory

Alternative approach for description of the non-equilibrium phenomena arising in solids at a severe external loading is analyzed. The approach is based on the new form of kinetic equations in terms of the internal and modified free energy. It is illustrated by a model example of a solid with vacancies, for which there is a complete statistical ground. The approach is applied to the description of important practical problem - the formation of fine-grained structure of metals during their treatment by methods of severe plastic deformation. In the framework of two-level two-mode effective internal energy potential model the strengthening curves unified for the whole of deformation range and containing the Hall-Petch and linear strengthening sections are calculated.Comment: 7 pages, 1 figur

Deficient prefrontal attentional control in late-life generalized anxiety disorder: an fMRI investigation

Younger adults with anxiety disorders are known to show an attentional bias toward negative information. Little is known regarding the role of biased attention in anxious older adults, and even less is known about the neural substrates of any such bias. Functional magnetic resonance imaging (fMRI) was used to assess the mechanisms of attentional bias in late life by contrasting predictions of a top-down model emphasizing deficient prefrontal cortex (PFC) control and a bottom-up model emphasizing amygdalar hyperreactivity. In all, 16 older generalized anxiety disorder (GAD) patients (mean age=66 years) and 12 non-anxious controls (NACs; mean age=67 years) completed the emotional Stroop task to assess selective attention to negative words. Task-related fMRI data were concurrently acquired. Consistent with hypotheses, GAD participants were slower to identify the color of negative words relative to neutral, whereas NACs showed the opposite bias, responding more quickly to negative words. During negative words (in comparison with neutral), the NAC group showed PFC activations, coupled with deactivation of task-irrelevant emotional processing regions such as the amygdala and hippocampus. By contrast, GAD participants showed PFC decreases during negative words and no differences in amygdalar activity across word types. Across all participants, greater attentional bias toward negative words was correlated with decreased PFC recruitment. A significant positive correlation between attentional bias and amygdala activation was also present, but this relationship was mediated by PFC activity. These results are consistent with reduced prefrontal attentional control in late-life GAD. Strategies to enhance top-down attentional control may be particularly relevant in late-life GAD treatment

The use of phylogeny to interpret cross-cultural patterns in plant use and guide medicinal plant discovery: an example from Pterocarpus (Leguminosae)

The study of traditional knowledge of medicinal plants has led to discoveries that have helped combat diseases and improve healthcare. However, the development of quantitative measures that can assist our quest for new medicinal plants has not greatly advanced in recent years. Phylogenetic tools have entered many scientific fields in the last two decades to provide explanatory power, but have been overlooked in ethnomedicinal studies. Several studies show that medicinal properties are not randomly distributed in plant phylogenies, suggesting that phylogeny shapes ethnobotanical use. Nevertheless, empirical studies that explicitly combine ethnobotanical and phylogenetic information are scarce.In this study, we borrowed tools from community ecology phylogenetics to quantify significance of phylogenetic signal in medicinal properties in plants and identify nodes on phylogenies with high bioscreening potential. To do this, we produced an ethnomedicinal review from extensive literature research and a multi-locus phylogenetic hypothesis for the pantropical genus Pterocarpus (Leguminosae: Papilionoideae). We demonstrate that species used to treat a certain conditions, such as malaria, are significantly phylogenetically clumped and we highlight nodes in the phylogeny that are significantly overabundant in species used to treat certain conditions. These cross-cultural patterns in ethnomedicinal usage in Pterocarpus are interpreted in the light of phylogenetic relationships.This study provides techniques that enable the application of phylogenies in bioscreening, but also sheds light on the processes that shape cross-cultural ethnomedicinal patterns. This community phylogenetic approach demonstrates that similar ethnobotanical uses can arise in parallel in different areas where related plants are available. With a vast amount of ethnomedicinal and phylogenetic information available, we predict that this field, after further refinement of the techniques, will expand into similar research areas, such as pest management or the search for bioactive plant-based compounds