27 research outputs found
First Record Of Parvodinium Umbonatum (stein) Carty (peridiniaceae, Dinophyta) For Northeast Brazil
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)This paper presents the first record of the freshwater dinoflagellate Parvodinium umbonatum (Stein) Carty (Peridiniaceae, Dinophyta) for northeast Brazil, based on samples collected in 2015 from a tank bromeliads at Serra da Jiboia, Bahia. This species was an important component in the local phytotelm community and categorized as frequent in the bromeliads of the area. A description based on morphometrical features, illustrations (LM and SEM), abiotic conditions of the stored water, and geographic distribution of P. umbonatum in Brazil are provided. © 2016 Check List and Authors.126CNPq, Conselho Nacional de Desenvolvimento Científico e TecnológicoFAPESB, Fundação de Amparo à Pesquisa do Estado da BahiaBOL0513/2014, FAPESB, Fundação de Amparo à Pesquisa do Estado da BahiaConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq
The BES f_0(1810): a new glueball candidate
We analyze the f_0(1810) state recently observed by the BES collaboration via
radiative J/\psi decay to a resonant \phi\omega spectrum and confront it with
DM2 data and glueball theory. The DM2 group only measured \omega\omega decays
and reported a pseudoscalar but no scalar resonance in this mass region. A
rescattering mechanism from the open flavored KKbar decay channel is considered
to explain why the resonance is only seen in the flavor asymmetric \omega\phi
branch along with a discussion of positive C parity charmonia decays to
strengthen the case for preferred open flavor glueball decays. We also
calculate the total glueball decay width to be roughly 100 MeV, in agreement
with the narrow, newly found f_0, and smaller than the expected estimate of
200-400 MeV. We conclude that this discovered scalar hadron is a solid glueball
candidate and deserves further experimental investigation, especially in the
K-Kbar channel. Finally we comment on other, but less likely, possible
assignments for this state.Comment: 11 pages, 4 figures. Major substantive additions, including an
ab-initio, QCD-based computation of the glueball inclusive decay width,
evaluation of final state effects, and enhanced discussion of several
alternative possibilities. Our conclusions are unchanged: the BES f_0(1810)
is a promising glueball candidat
The Theta+ (1540) as a heptaquark with the overlap of a pion, a kaon and a nucleon
We study the very recently discovered Theta+ (1540) at SPring-8, at ITEP and
at CLAS-Thomas Jefferson Lab. We apply the same RGM techniques that already
explained with success the repulsive hard core of nucleon-nucleon, kaon-nucleon
exotic scattering, and the attractive hard core present in pion-nucleon and
pion-pion non-exotic scattering. We find that the K-N repulsion excludes the
Theta+ as a K-N s-wave pentaquark. We explore the Theta+ as a heptaquark,
equivalent to a N+pi+K borromean bound-state, with positive parity and total
isospin I=0. We find that the kaon-nucleon repulsion is cancelled by the
attraction existing both in the pion-nucleon and pion-kaon channels. Although
we are not yet able to bind the total three body system, we find that the
Theta^+ may still be a heptaquark state. We conclude with predictions that can
be tested experimentally.Comment: 5 pages, 5 figures, 2 tables, submitted to Phys. Rev. D, rapid
communicatio
A Naturally Narrow Positive Parity Theta^+
We present a consistent color-flavor-spin-orbital wave function for a
positive parity Theta^+ that naturally explains the observed narrowness of the
state. The wave function is totally symmetric in its flavor-spin part and
totally antisymmetric in its color-orbital part. If flavor-spin interactions
dominate, this wave function renders the positive parity Theta^+ lighter than
its negative parity counterpart. We consider decays of the Theta^+ and compute
the overlap of this state with the kinematically allowed final states. Our
results are numerically small. We note that dynamical correlations between
quarks are not necessary to obtain narrow pentaquark widths.Comment: 10 pages, 1 figure, Revtex4, two-column format, version to be
published in Phys. Rev. D, includes numerical estimates of decay width
Z^* Resonances: Phenomenology and Models
We explore the phenomenology of, and models for, the Z^* resonances, the
lowest of which is now well established, and called the Theta. We provide an
overview of three models which have been proposed to explain its existence
and/or its small width, and point out other relevant predictions, and potential
problems, for each. The relation to what is known about KN scattering,
including possible resonance signals in other channels, is also discussed.Comment: 29 pages, uses RevTeX4; expanded version (published form
Feeding strategies and energy to protein ratio on tambaqui performance and physiology
The objective of this work was to evaluate the effect of feed deprivation and refeeding with diets containing different energy to protein ratios (E/P) on the performance and physiology of juvenile tambaqui (Colossoma macropomum). A 4x2 factorial arrangement with three replicates was used, with four E/P ratios (11.5, 10.5, 9.5, and 8.5 kcal g-1 digestible energy per protein) and two feeding regimens (with and without deprivation), during 60 days. Fish from the food-deprived group were fasted for 14 days and refed from the fifteenth to the sixtieth day, whereas the remaining fish were fed for 60 days. At the end of the experimental period, weight of fish subjected to food deprivation was lower than that of those continuously fed; however, this condition did not influence the physiological parameters analyzed. Tambaqui fed 11.5 kcal g-1 achieved lower final weight than those fed with the other diets, in both regimens. Among the physiological parameters, only plasma protein presented significant increase in fish fed 8.5 kcal g-1, in both feeding regimens, probably due to the higher dietary protein concentration. These results indicate that fish show a partial compensatory growth, and that 10.5 kcal g-1 can be recommended for the diet of juvenile tambaqui