119 research outputs found
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 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 for which represents the coupling of high
mass scalar meson -> two pseudoscalar mesons are almost same as the
coupling for the I=0. On the other hand, the coupling constant for
which represents the low mass scalar meson -> are far
from the coupling constant for I=0. We consider a resolution for this
discrepancy. Coupling constant for glueball -> is smaller than
the coupling . is .Comment: 15 pages, 6 figure
Tri-meson-mixing of -- and -- in the light-cone quark model
The radiative transition form factors of the pseudoscalar mesons {,
, } and the vector mesons {, , } are restudied
with -- and -- 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 - mixing and - mixing.Comment: 8 pages, 6 figures, final version to appear in EPJ
Activity, habitat use, feeding behavior, and diet of four sympatric species of Serranidae (Actinopterygii: Perciformes) in southeastern Brazil
Phylogeography of the tropical planktonic foraminifera lineage Globigerinella reveals isolation inconsistent with passive dispersal by ocean currents
Morphologically defined species of marine plankton often harbor a considerable level of cryptic diversity. Since many morphospecies show cosmopolitan distribution, an understanding of biogeographic and evolutionary processes at the level of genetic diversity requires global sampling. We use a database of 387 single-specimen sequences of the SSU rDNA of the planktonic foraminifera Globigerinella as a model to assess the biogeographic and phylogenetic distributions of cryptic diversity in marine microplankton on a global scale. Our data confirm the existence of multiple, well isolated genetic lineages. An analysis of their abundance and distribution indicates that our sampling is likely to approximate the actual total diversity. Unexpectedly, we observe an uneven allocation of cryptic diversity among the phylogenetic lineages. We show that this pattern is neither an artifact of sampling intensity nor a function of lineage age. Instead, we argue that it reflects an ongoing speciation process in one of the three major lineages. Surprisingly, four of the six genetic types in the hyperdiverse lineage are biogeographically restricted to the Indopacific. Their mutual co-occurrence and their hierarchical phylogenetic structure provide no evidence for an origin through sudden habitat fragmentation and their limitation to the Indopacific challenges the view of a global gene flow within the warm-water provinces. This phenomenon shows that passive dispersal is not sufficient to describe the distribution of plankton diversity. Rather, these organisms show differentiated distribution patterns shaped by species interactions and reflecting phylogenetic contingency with unique histories of diversification rates
3D: diversity, dynamics, differential testing â a proposed pipeline for analysis of next-generation sequencing T cell repertoire data
Contribuição ao manejo sustentåvel do complexo ferruginoso nectandra na floresta nacional de Ibirama, SC
Spreading speeds of invasive species in a periodic patchy environment: effects of dispersal based on local information and gradient-based taxis
Population dynamics and spatial distribution of Abaris basistriata Chaudoir, 1873 (Coleoptera: Carabidae)
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