Evaluated Experimental Isobaric Analogue States from T=1/2T = 1/2 to T=3T = 3 and associated IMME coefficients

Isobaric multiplets can be used to provide reliable mass predictions through the Isobaric Multiplet Mass Equation (IMME). Isobaric analogue states (IAS) for isospin multiplets from $T=1/2$ to $T=3$ have been studied within the 2012 Atomic Mass Evaluation (Ame2012). Each IAS established from published experimental reaction data has been expressed in the form of a primary reaction $Q$-value, and if necessary, has been recalibrated. The evaluated IAS masses are provided here along with the associated IMME coefficients. Quadratic and higher order forms of the IMME have been considered, and global trends have been extracted. Particular nuclides, requiring experimental investigation, have been identified and discussed. This dataset is the most precise and extensive set of evaluated IAS to date.Comment: 44 pages, 7 figures, 11 tables. Accepted for publication in Nuclear Physics

Reply to Comment on Extension of the Bethe-Weizsacker mass formula to light nuclei and some new shell closures

Some properties of the modified Bethe-Weizsacker mass formula (BWM) are discussed. As BWM has no shell effect included, the extra-stability or, magicity in nuclei clearly stands out when experimental mass data are compared with BWM predictions. If the shell effect quenches, the BWM predictions come closer to the experimental data.Comment: 2 pages, no figur

Deformation Projected RMF Calculation for Cr and Fe nuclei in Hybrid Derivative Coupling Model

The ground state properties of even mass Cr and Fe isotopes are studied using the generalized hybrid derivative coupling model. The energy surface of each isotope is plotted as a function of the mass quadrupole moment. The neutron numbers N=20 and N=40 are seen to remain magic numbers but N= 28 and 50 are predicted to be non-magic. The neutron number N=70 turns out to be a magic number according to the present calculation. In all the isotopes studied the calculated binding energy values are less than those obtained from experiment while the deformation is in better agreement.Comment: To appear in Int. Jour. Mod. Phys.

Fermionic Molecular Dynamics for nuclear dynamics and thermodynamics

A new Fermionic Molecular Dynamics (FMD) model based on a Skyrme functional is proposed in this paper. After introducing the basic formalism, some first applications to nuclear structure and nuclear thermodynamics are presentedComment: 5 pages, Proceedings of the French-Japanese Symposium, September 2008. To be published in Int. J. of Mod. Phys.

Accurate mass measurements of 26^{26}Ne, 26−30^{26-30}Na, 29−33^{29-33}Mg performed with the {\sc Mistral} spectrometer

The minuteness of the nuclear binding energy requires that mass measurements be highly precise and accurate. Here we report on new measurements $^{29-33}$Mg and $^{26}$Na performed with the {\sc Mistral} mass spectrometer at {\sc Cern}'s {\sc Isolde} facility. Since mass measurements are prone to systematic errors, considerable effort has been devoted to their evaluation and elimination in order to achieve accuracy and not only precision. We have therefore conducted a campaign of measurements for calibration and error evaluation. As a result, we now have a satisfactory description of the {\sc Mistral} calibration laws and error budget. We have applied our new understanding to previous measurements of $^{26}$Ne, $^{26-30}$Na and $^{29,32}$Mg for which re-evaluated values are reported.Comment: submitted to Nuclear Physics

The AME2003 atomic mass evaluation (I) - Evaluation of input data, adjustment procedures

This paper is the first of two parts presenting the result of a new evaluation of atomic masses (Ame2003). In this first part we give full information on the used and rejected input data and on the procedures used in deriving the tables in the second part. We first describe the philosophy and procedures used in selecting nuclear-reaction, decay, and mass spectrometric results as input values in a least-squares evaluation of best values for atomic masses. The calculation procedures and particularities of the Ame are then described. All accepted data, and rejected ones with a reported precision still of interest, are presented in a table and compared there with the adjusted values. The differences with the earlier evaluation are briefly discussed and information is given of interest for the users of this Ame. The second paper for the Ame2003, last in this issue, gives a table of atomic masses, tables and graphs of derived quantities, and the list of references used in both this evaluation and the Nubase2003 table (first paper in this issue)

On the nucleon-nucleon interaction leading to a standing wave instability in symmetric nuclear matter

We examine a recently proposed nucleon-nucleon interaction, claimed by its authors both realistic and leading to a standing wave instability in symmetric nuclear matter. Contrary to these claims, we find that this interaction leads to a serious overbinding of 4He, 16O and 40Ca nuclei when the Hartree-Fock method is properly applied. The resulting nuclear densities contradict the experimental data and all realistic Hartree-Fock results.Comment: 4 pages, 1 figur

Understanding the in vivo Uptake Kinetics of a Phosphatidylethanolamine-binding Agent \u3csup\u3e99m\u3c/sup\u3eTc-Duramycin

Introduction 99mTc-Duramycin is a peptide-based molecular probe that binds specifically to phosphatidylethanolamine (PE). The goal was to characterize the kinetics of molecular interactions between 99mTc-Duramycin and the target tissue. Methods High level of accessible PE is induced in cardiac tissues by myocardial ischemia (30 min) and reperfusion (120 min) in Sprague–Dawley rats. Target binding and biodistribution of 99mTc-duramycin were captured using SPECT/CT. To quantify the binding kinetics, the presence of radioactivity in ischemic versus normal cardiac tissues was measured by gamma counting at 3, 10, 20, 60 and 180 min after injection. A partially inactivated form of 99mTc-Duramycin was analyzed in the same fashion. A compartment model was developed to quantify the uptake kinetics of 99mTc-Duramycin in normal and ischemic myocardial tissue. Results 99mTc-duramycin binds avidly to the damaged tissue with a high target-to-background radio. Compartment modeling shows that accessibility of binding sites in myocardial tissue to 99mTc-Duramycin is not a limiting factor and the rate constant of target binding in the target tissue is at 2.2 ml/nmol/min/g. The number of available binding sites for 99mTc-Duramycin in ischemic myocardium was estimated at 0.14 nmol/g. Covalent modification of D15 resulted in a 9-fold reduction in binding affinity. Conclusion 99mTc-Duramycin accumulates avidly in target tissues in a PE-dependent fashion. Model results reflect an efficient uptake mechanism, consistent with the low molecular weight of the radiopharmaceutical and the relatively high density of available binding sites. These data help better define the imaging utilities of 99mTc-Duramycin as a novel PE-binding agent