Deuteron-equivalent and phase-equivalent interactions within light nuclei

Background: Phase-equivalent transformations (PETs) are well-known in quantum scattering and inverse scattering theory. PETs do not affect scattering phase shifts and bound state energies of two-body system but are conventionally supposed to modify two-body bound state observables such as the rms radius and electromagnetic moments. Purpose: In order to preserve all bound state observables, we propose a new particular case of PETs, a deuteron-equivalent transformation (DET-PET), which leaves unchanged not only scattering phase shifts and bound state (deuteron) binding energy but also the bound state wave function. Methods: The construction of DET-PET is discussed; equations defining the simplest DET-PETs are derived. We apply these simplest DET-PETs to the JISP16 $NN$ interaction and use the transformed $NN$ interactions in calculations of $^3$H and $^4$He binding energies in the No-core Full Configuration (NCFC) approach based on extrapolations of the No-core Shell Model (NCSM) basis space results to the infinite basis space. Results: We demonstrate the DET-PET modification of the $np$ scattering wave functions and study the DET-PET manifestation in the binding energies of $^3$H and $^4$He nuclei and their correlation (Tjon line). Conclusions: It is shown that some DET-PETs generate modifications of the central component while the others modify the tensor component of the $NN$ interaction. DET-PETs are able to modify significantly the $np$ scattering wave functions and hence the off-shell properties of the $NN$ interaction. DET-PETs give rise to significant changes in the binding energies of $^3$H (in the range of approximately 1.5 MeV) and $^4$He (in the range of more than 9 MeV) and are able to modify the correlation patterns of binding energies of these nuclei

Ultra-low field NMR relaxometry : calibration method and acquisition of T1-dispersion curves from biological samples extended to the region of μT

Non peer reviewedPublisher PD

Multi-channel phase-equivalent transformation and supersymmetry

Phase-equivalent transformation of local interaction is generalized to the multi-channel case. Generally, the transformation does not change the number of the bound states in the system and their energies. However, with a special choice of the parameters, the transformation removes one of the bound states and is equivalent to the multi-channel supersymmetry transformation recently suggested by Sparenberg and Baye. Using the transformation, it is also possible to add a bound state to the discrete spectrum of the system at a given energy $E<0$ if the angular momentum at least in one of the coupled channels $l\ge 2$.Comment: 9 pages, revtex; to be published in Phys. At. Nucl. (Oct. 2000

Fast Field-Cycling MRI : Demonstration of New Technology for T1-Dispersion Contrast

Peer reviewedPublisher PD

Nucleon-nucleon interaction in the JJ-matrix inverse scattering approach and few-nucleon systems

The nucleon-nucleon interaction is constructed by means of the $J$-matrix version of inverse scattering theory. Ambiguities of the interaction are eliminated by postulating tridiagonal and quasi-tridiagonal forms of the potential matrix in the oscillator basis in uncoupled and coupled waves, respectively. The obtained interaction is very accurate in reproducing the $NN$ scattering data and deuteron properties. The interaction is used in the no-core shell model calculations of $^3$H and $^4$He nuclei. The resulting binding energies of $^3$H and $^4$He are very close to experimental values.Comment: Text is revised, new figures and references adde

Inverse scattering J-matrix approach to nucleon-nucleus scattering and the shell model

The $J$-matrix inverse scattering approach can be used as an alternative to a conventional $R$-matrix in analyzing scattering phase shifts and extracting resonance energies and widths from experimental data. A great advantage of the $J$-matrix is that it provides eigenstates directly related to the ones obtained in the shell model in a given model space and with a given value of the oscillator spacing $\hbar\Omega$. This relationship is of a particular interest in the cases when a many-body system does not have a resonant state or the resonance is broad and its energy can differ significantly from the shell model eigenstate. We discuss the $J$-matrix inverse scattering technique, extend it for the case of charged colliding particles and apply it to the analysis of $n\alpha$ and $p\alpha$ scattering. The results are compared with the No-core Shell Model calculations of $^5$He and $^5$Li.Comment: Some text is added following suggestions of a journal refere

On isovector meson exchange currents in the Bethe-Salpeter approach

We investigate the nonrelativistic reduction of the Bethe-Salpeter amplitude for the deuteron electrodisintegration near threshold energies. To this end, two assumptions have been used in the calculations: 1) the static approximation and 2) the one iteration approximation. Within these assumptions it is possible to recover the nonrelativistic result including a systematic extension to relativistic corrections. We find that the so-called pair current term can be constructed from the $P$-wave contribution of the deuteron Bethe-Salpeter amplitude. The form factor that enters into the calculation of the pair current is constrained by the manifestly gauge independent matrix elements.Comment: 15 pages, incl. 3 figures, to be published Phys. Rev.

NN potentials from inverse scattering in the J-matrix approach

An approximate inverse scattering method [7,8] has been used to construct separable potentials with the Laguerre form factors. As an application, we invert the phase shifts of proton-proton in the $^1S_0$ and $^3P_2-^3F_2$ channels and neutron-proton in the $^3S_1-^3D_1$ channel elastic scattering. In the latter case the deuteron wave function of a realistic $np$ potential was used as input.Comment: LaTex2e, 17 pages, 3 Postscript figures; corrected typo

Functional characterization of a melon alcohol acyl-transferase gene family involved in the biosynthesis of ester volatiles. Identification of the crucial role of a threonine residue for enzyme activity

Volatile esters, a major class of compounds contributing to the aroma of many fruit, are synthesized by alcohol acyl-transferases (AAT). We demonstrate here that, in Charentais melon (Cucumis melo var. cantalupensis), AAT are encoded by a gene family of at least four members with amino acid identity ranging from 84% (Cm-AAT1/Cm-AAT2) and 58% (Cm-AAT1/Cm-AAT3) to only 22% (Cm-AAT1/Cm-AAT4). All encoded proteins, except Cm-AAT2, were enzymatically active upon expression in yeast and show differential substrate preferences. Cm-AAT1 protein produces a wide range of short and long-chain acyl esters but has strong preference for the formation of E-2-hexenyl acetate and hexyl hexanoate. Cm-AAT3 also accepts a wide range of substrates but with very strong preference for producing benzyl acetate. Cm-AAT4 is almost exclusively devoted to the formation of acetates, with strong preference for cinnamoyl acetate. Site directed mutagenesis demonstrated that the failure of Cm-AAT2 to produce volatile esters is related to the presence of a 268-alanine residue instead of threonine as in all active AAT proteins. Mutating 268-A into 268-T of Cm-AAT2 restored enzyme activity, while mutating 268-T into 268-A abolished activity of Cm-AAT1. Activities of all three proteins measured with the prefered substrates sharply increase during fruit ripening. The expression of all Cm-AAT genes is up-regulated during ripening and inhibited in antisense ACC oxidase melons and in fruit treated with the ethylene antagonist 1-methylcyclopropene (1-MCP), indicating a positive regulation by ethylene. The data presented in this work suggest that the multiplicity of AAT genes accounts for the great diversity of esters formed in melon

Effective Lagrangian Approach to the Theory of Eta Photoproduction in the N∗(1535)N^{*}(1535) Region

We investigate eta photoproduction in the $N^{*}(1535)$ resonance region within the effective Lagrangian approach (ELA), wherein leading contributions to the amplitude at the tree level are taken into account. These include the nucleon Born terms and the leading $t$-channel vector meson exchanges as the non-resonant pieces. In addition, we consider five resonance contributions in the $s$- and $u$- channel; besides the dominant $N^{*}(1535)$, these are: $N^{*}(1440),N^{*}(1520),N^{*}(1650)$ and $N^{*}(1710)$. The amplitudes for the $\pi^\circ$ and the $\eta$ photoproduction near threshold have significant differences, even as they share common contributions, such as those of the nucleon Born terms. Among these differences, the contribution to the $\eta$ photoproduction of the $s$-channel excitation of the $N^{*}(1535)$ is the most significant. We find the off-shell properties of the spin-3/2 resonances to be important in determining the background contributions. Fitting our effective amplitude to the available data base allows us to extract the quantity $\sqrt{\chi \Gamma_\eta} A_{1/2}/\Gamma_T$, characteristic of the photoexcitation of the $N^{*}(1535)$ resonance and its decay into the $\eta$-nucleon channel, of interest to precise tests of hadron models. At the photon point, we determine it to be $(2.2\pm 0.2)\times 10^{-1} GeV^{-1}$ from the old data base, and $(2.2\pm 0.1) \times 10^{-1} GeV^{-1}$ from a combination of old data base and new Bates data. We obtain the helicity amplitude for $N^{*}(1535)\rightarrow \gamma p$ to be $A_{1/2}=(97\pm 7)\times 10^{-3} GeV^{-1/2}$ from the old data base, and $A_{1/2}=(97\pm 6)\times 10^{-3} GeV^{-1/2}$ from the combination of the old data base and new Bates data, compared with the results of the analysis of pion photoproduction yielding $74\pm 11$, in the same units.Comment: 43 pages, RevTeX, 9 figures available upon request, to appear in Phys. Rev.