123 research outputs found

    Spectrum of the Y=2 Pentaquarks

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    By assuming a mass formula for the spectrum of the Y=2 pentaquarks, where the chromo-magnetic interaction plays a main role, and identifying the lightest state with the Theta^+(1540), we predict a spectrum in good agreement with the few I=0 and I=1 candidates proposed in the past.Comment: 12 pages, 4 figures, LaTe

    Some (further) Comments on the Theta(1540) Pentaquark

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    Additional broader I=0 states in the KN channel near Ī˜+\Theta^+(1540) are expected in many models, making the absence of any signature in the K+^+-deuteron scattering data even more puzzling. In an ideal "three-body" picture the Ī˜\Theta is viewed as two compact ud(1)ud(2) 3Ė‰\bar{3} color diquarks and an sĖ‰\bar{s} quark. A "QCD-type" inequality involving m(Ī˜+),m(Ī›)m(\Theta^+), m(\Lambda), the mass of the Ī›(1/2āˆ’)\Lambda(1/2^-) L=1 excitation and that of a new I=0 tetraquark vector meson then follows. The inequality suggests a very light new vector meson, and is violated. We note that "associated production" of the pentaquark with another quadriquark or anti-pentaquark may be favored. This along with some estimates of the actual production cross sections suggest that the Ī˜\Theta can be found in BaBar or Belle e+^+-eāˆ’^- colliders.Comment: 6 page

    Pentaquark as Kaon-Nucleon Resonance

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    Several recent experiments have reported evidence for a narrow feature in the K(+)-neutron system, an apparent resonant state ~ 100 MeV above threshold and with a width < 25 MeV. This state has been labelled as Theta(+) (previously as Z(*)), and because of the implied inclusion of a anti-strange quark, is referred to as a pentaquark, that is, five quarks within a single bag. We present an alternative explanation for such a structure, as a higher angular momentum resonance in the isospin zero K(+) -N system. One might call this an exit channel or a molecular resonance. In a non-relativistic potential model we find a possible candidate for the kaon-nucleon system with relative angular momentum L=3, while L=1 and 2 states possess centrifugal barriers too low to confine the kaon and nucleon in a narrow state at an energy so high above threshold. A rather strong state-dependence in the potential is essential, however, for eliminating an observable L=2 resonance at lower energies.Comment: 4 page

    A-dependence of nuclear transparency in quasielastic A(e,e'p) at high Q^2

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    The A-dependence of the quasielastic A(e,e'p) reaction has been studied at SLAC with H-2, C, Fe, and Au nuclei at momentum transfers Q^2 = 1, 3, 5, and 6.8 (GeV/c)^2. We extract the nuclear transparency T(A,Q^2), a measure of the average probability that the struck proton escapes from the nucleus A without interaction. Several calculations predict a significant increase in T with momentum transfer, a phenomenon known as Color Transparency. No significant rise within errors is seen for any of the nuclei studied.Comment: 5 pages incl. 2 figures, Caltech preprint OAP-73

    A Naturally Narrow Positive Parity Theta^+

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    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

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    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

    Seasonal cycle of CO2 from the sea ice edge to island blooms in the Scotia Sea, Southern Ocean

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    The Scotia Sea region contains some of the most productive waters of the Southern Ocean. It is also a dynamic region through the interaction of deep water masses with the atmosphere. We present a first seasonally-resolved time series of the fugacity of CO2 (fCO2) from spring 2006, summer 2008, autumn 2009 and winter (potential temperature minimum) along a 1000 km transect from the pack ice to the Polar Front to quantify the effects of biology and temperature on oceanic fCO2. Substantial spring and summer decreases in sea surface fCO2 occurred in phytoplankton blooms that developed in the naturally iron fertilised waters downstream (north) of South Georgia island (54-55S, 36-38W) and following sea ice melt (in the seasonal ice zone). The largest seasonal fCO2 amplitude (fCO2) of 159 uatm was found in the South Georgia bloom. In this region, biological carbon uptake dominated the seasonal signal, reducing the winter maxima in oceanic fCO2 by 257 uatm by the summer. In the Weddell-Scotia Confluence, the southern fringe of the Scotia Sea, the shift from wintertime CO2-rich conditions in ice covered waters to CO2 undersaturation in the spring blooms during and upon sea ice melt created strong seasonality in oceanic fCO2. Temperature effects on oceanic fCO2 ranged from fCO2sst of 55 uatm in the seasonal ice zone to almost double that downstream of South Georgia (98 uatm). The seasonal cycle of surface water fCO2 in the high-nutrient low-chlorophyll region of the central Scotia Sea had the weakest biological control and lowest seasonality. Basin-wide biological processes dominated the seasonal control on oceanic fCO2 (fCO2bio of 159 Ī¼atm), partially compensated (43%) by moderate temperature control (fCO2sst of 68 Ī¼atm). The patchwork of productivity across the Scotia Sea creates regions of seasonally strong biological uptake of CO2 in the Southern Ocean
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