Mixing among light scalar mesons and L=1 q\bar{q} scalar mesons

Following the re-establishment of the \sigma(600) and the \kappa(900), the light scalar mesons a_0(980) and f_0(980) together with the \sigma(600) and the \kappa(900) are considered as the chiral scalar partner of pseudoscalar nonet in SU(3) chiral symmetry, and the high mass scalar mesons a_0(1450), K^*_0(1430), f_0(1370) and f_0(1710) turned out to be considered as the L=1 q\bar{q} scalar mesons. We assume that the high mass of the L=1 q\bar{q} scalar mesons is caused by the mixing with the light scalar mesons. For the structure of the light scalar mesons, we adopted the qq\bar{q}\bar{q} model in order to explain the "scalar meson puzzle". The inter-mixing between the light scalar nonet and the high mass L=1 q\bar{q} nonet and the intra-mixing among each nonet are analyzed by including the glueball into the high mass scalar nonet.Comment: 16 pages, 5 figure

Effects to Scalar Meson Decays of Strong Mixing between Low and High Mass Scalar Mesons

We analyze the mass spectroscopy of low and high mass scalar mesons and get the result that the coupling strengths of the mixing between low and high mass scalar mesons are very strong and the strengths of mixing for $I=1, 1/2$ scalar mesons and those of I=0 scalar mesons are almost same. Next, we analyze the decay widths and decay ratios of these mesons and get the results that the coupling constants $A'$ for $I=1, 1/2$ which represents the coupling of high mass scalar meson $N'$ -> two pseudoscalar mesons $PP$ are almost same as the coupling $A'$ for the I=0. On the other hand, the coupling constant $A$ for $I=1, I=1/2$ which represents the low mass scalar meson $N$ -> $PP$ are far from the coupling constant $A$ for I=0. We consider a resolution for this discrepancy. Coupling constant $A''$ for glueball $G$ -> $PP$ is smaller than the coupling $A'$. $\theta_P$ is $40^\circ \sim 50^\circ$.Comment: 15 pages, 6 figure

Tri-meson-mixing of π\pi-η\eta-η′\eta' and ρ\rho-ω\omega-ϕ\phi in the light-cone quark model

The radiative transition form factors of the pseudoscalar mesons {$\pi$, $\eta$, $\eta'$} and the vector mesons {$\rho$, $\omega$, $\phi$} are restudied with $\pi$-$\eta$-$\eta'$ and $\rho$-$\omega$-$\phi$ in tri-meson-mixing pattern, which is described by tri-mixing matrices in the light-cone constituent quark model. The experimental transition decay widths are better reproduced with tri-meson-mixing than previous results in a two-mixing-angle scenario of only two-meson $\eta$-$\eta'$ mixing and $\omega$-$\phi$ mixing.Comment: 8 pages, 6 figures, final version to appear in EPJ

J/psi->VP decays and the quark and gluon content of the eta and eta'

The $\eta$-$\eta^\prime$ pseudoscalar mixing angle and the gluonium content of the $\eta^\prime$ meson are deduced from an updated phenomenological analysis of $J/\psi$ decays into a vector and a pseudoscalar meson. In absence of gluonium, the value of the mixing angle in the quark-flavour basis is found to be $\phi_P=(40.7\pm 2.3)^\circ$. In presence of gluonium, the values for the mixing angle and the gluonic content of the $\eta^\prime$ wave function are $\phi_P=(44.6\pm 4.4)^\circ$ and $Z^2_{\eta^\prime}=0.29^{+0.18}_{-0.26}$, respectively. The newly reported values of $B(J/\psi\to\rho\pi)$ by the BABAR and BES Collaborations are crucial to get a consistent description of data.Comment: 7 pages, 1 figure, uses svjour style. Comments on the relationship between J/psi to VP and V to Pgamma decays and on the neglected contributions together with an asymmetric treatment of errors are include

Decadal Effects of Thinning on Understory Light Environments and Plant Community Structure in a Subtropical Forest

Canopy-opening disturbance such as thinning has immediate and substantive effects on understory microclimate and therefore the establishment and growth of understory plants. A large number of studies have reported the effects of thinning on tree growth, but few studies have examined long-term effects of thinning on understory light environments and species and functional diversity of understory plants. Even less is known whether the change in understory plant community structure observed following canopy disturbance is short-lived and would diminish as the canopy closes or a long lasting due to legacy effects. We examined the effects of an experimental removal of 25% and 50% of the woody vegetation on understory light availability and variability on understory plant community structure in a subtropical Cryptomeria japonica plantation nine years after the treatment. Differences in availability of understory light among treatments diminished nine years after the experimental vegetation removal (thinning), but variability of understory light was still two times higher in the thinned treatments than the un-thinned control. Species diversity of dominant and common understory plants was lower in the control than in the two thinning treatments, which were not different from each other. Community species and functional composition were also different between the un-thinned control and the two thinning treatments. The thinned plots had proportionally more individuals of grasses and forbs and fewer individuals of ferns. Our results indicate that the effects of thinning on understory light variability last longer than on light availability representing an important and long-lasting alteration of resource heterogeneity. At both species and functional group levels, greater diversity and unique composition in the thinned treatments compared to undisturbed control suggest a link between resource heterogeneity and biodiversity in the forest understory or legacy effects associated with the thinning-induced changes in understory plant community

Gaze fixation improves the stability of expert juggling

Novice and expert jugglers employ different visuomotor strategies: whereas novices look at the balls around their zeniths, experts tend to fixate their gaze at a central location within the pattern (so-called gaze-through). A gaze-through strategy may reflect visuomotor parsimony, i.e., the use of simpler visuomotor (oculomotor and/or attentional) strategies as afforded by superior tossing accuracy and error corrections. In addition, the more stable gaze during a gaze-through strategy may result in more accurate movement planning by providing a stable base for gaze-centered neural coding of ball motion and movement plans or for shifts in attention. To determine whether a stable gaze might indeed have such beneficial effects on juggling, we examined juggling variability during 3-ball cascade juggling with and without constrained gaze fixation (at various depths) in expert performers (n = 5). Novice jugglers were included (n = 5) for comparison, even though our predictions pertained specifically to expert juggling. We indeed observed that experts, but not novices, juggled significantly less variable when fixating, compared to unconstrained viewing. Thus, while visuomotor parsimony might still contribute to the emergence of a gaze-through strategy, this study highlights an additional role for improved movement planning. This role may be engendered by gaze-centered coding and/or attentional control mechanisms in the brain

Spatially Explicit Analyses of Anopheline Mosquitoes Indoor Resting Density: Implications for Malaria Control

Background: The question of sampling and spatial aggregation of malaria vectors is central to vector control efforts and estimates of transmission. Spatial patterns of anopheline populations are complex because mosquitoes' habitats and behaviors are strongly heterogeneous. Analyses of spatially referenced counts provide a powerful approach to delineate complex distribution patterns, and contributions of these methods in the study and control of malaria vectors must be carefully evaluated. Methodology/Principal Findings: We used correlograms, directional variograms, Local Indicators of Spatial Association (LISA) and the Spatial Analysis by Distance IndicEs (SADIE) to examine spatial patterns of Indoor Resting Densities (IRD) in two dominant malaria vectors sampled with a 565 km grid over a 2500 km(2) area in the forest domain of Cameroon. SADIE analyses revealed that the distribution of Anopheles gambiae was different from regular or random, whereas there was no evidence of spatial pattern in Anopheles funestus (Ia = 1.644, Pa0.05, respectively). Correlograms and variograms showed significant spatial autocorrelations at small distance lags, and indicated the presence of large clusters of similar values of abundance in An. gambiae while An. funestus was characterized by smaller clusters. The examination of spatial patterns at a finer spatial scale with SADIE and LISA identified several patches of higher than average IRD (hot spots) and clusters of lower than average IRD (cold spots) for the two species. Significant changes occurred in the overall spatial pattern, spatial trends and clusters when IRDs were aggregated at the house level rather than the locality level. All spatial analyses unveiled scale-dependent patterns that could not be identified by traditional aggregation indices. Conclusions/Significance: Our study illustrates the importance of spatial analyses in unraveling the complex spatial patterns of malaria vectors, and highlights the potential contributions of these methods in malaria control