Leading and higher twists in proton,neutron and deuteron unpolarized structure functions F<Subscript>2</Subscript>

We summarize the results of a recent global analysis of proton and deuteron F₂ structure function world data performed over a large range of kinematics, including recent measurements done at JLab with the CLAS detector. From these data the lowest moments (n≤10) of the unpolarized structure functions are determined with good statistics and systematics. The Q² evolution of the extracted moments is analyzed in terms of an OPE-based twist expansion, taking into account soft-gluon effects at large x. A clean separation among the leading- and higher-twist terms is achieved. By combining proton and deuteron measurements the lowest moments of the neutron F₂ structure function are determined and its leading-twist term is extracted. Particular attention is paid to nuclear effects in the deuteron, which become increasingly important for the higher moments. Our results for the non-singlet, isovector (p-n) combination of the leading-twist moments are used to test recent lattice simulations. We also determine the lowest few moments of the higher-twist contributions, and find these to be approximately isospin independent, suggesting the possible dominance of ud correlations over uu and dd in the nucleon.     

Extraction of bound-state parameters from dispersive sum rules

The procedure of extracting the ground-state parameters from vacuum-to-vacuum and vacuum-to-hadron correlators within the method of sum rules is considered. The emphasis is laid on the crucial ingredient of this method—the effective continuum threshold. A new algorithm to fix this quantity is proposed and tested. First, a quantum-mechanical potential model which provides the only possibility to probe the reliability and the actual accuracy of this method is used as a study case. In this model, our algorithm is shown to lead to a remarkable improvement of the accuracy of the extracted ground-state parameters compared to the standard procedures adopted in the method and used in all previous applications of dispersive sum rules in QCD. As a next step, it is demonstrated that the procedures of extracting the ground-state decay constant in the potential model and in QCD are quantitatively very close to each other. Therefore, the application of the proposed algorithm in QCD promises a considerable increase of the accuracy of the extracted hadron parameters.     

Kelvin waves of quantized vortex lines in trapped Bose-Einstein condensates

We have theoretically investigated Kelvin waves of quantized vortex lines in trapped Bose-Einstein condensates. Counterrotating perturbation induces an elliptical instability to the initially straight vortex line, driven by a parametric resonance between a quadrupole mode and a pair of Kelvin modes of opposite momenta. Subsequently, Kelvin waves rapidly decay to longer wavelengths emitting sound waves in the process. We present a modified Kelvin wave dispersion relation for trapped superfluids and propose a simple method to excite Kelvin waves of specific wave number.     

Calculations for few-body systems with correlated basis functions

A new variational method is applied to the solution of the Schrödinger equation for few-body systems. The results for three nucleons interacting via both the central and the spin-dependent Malfliet-Tjon interactions are presented and compared with Faddeev, ATMS and Green's Function Monte Carlo results.Presented at the symposium Mesons and Light Nuclei, Bechyn, Czechoslovakia, May 27–June 1, 1985.     

Nucleon-Nucleon Correlations and Six-Quark-Cluster Effects in Semi-Inclusive Deep-Inelastic Lepton Scattering off Few-Nucleon Systems

Semi-inclusive deep-inelastic Lepton scattering off few-nucleon systems is investigated assuming that virtual-boson absorption occurs on a hadronic cluster, which can be either a two-nucleon correlated pair or a six-quark bag. In both cases the relevance of nuclear effects on forward and backward nucleon emissions is illustrated and the differences expected in the energy distribution of the emitted nucleons are analyzed both at x < 1 and x > 1. Received March 31, 1994; revised August 29, 1994; accepted for publication September 12, 1994     

Aqueous Copper‐Mediated Living Radical Polymerisation of N‐Acryloylmorpholine,SET‐LRP in Water

The polymerisation of N‐acryloylmorpholine in water is reported utilising Cu(0)‐mediated living radical polymerisation (SET‐LRP). The inherent instability of [Cu^I(Me₆‐Tren)Br] in aqueous solution is exploited via rapid disproportionation to prepare Cu(0) particles and [Cu^II(Me₆‐Tren)Br₂] in situ prior to addition of monomer and initiator. Quantitative conversion is attained within 30 min for various degrees of polymerisation (DP_n = 20–640) with SEC showing symmetrical narrow molecular weight distributions (Đ < 1.18) in all cases. Optimised conditions are subsequently applied for the preparation of a diblock copolymer poly(NIPAm)‐b‐(N‐acryloylmorpholine), illustrating the versatility of this approach.

     

Mammalian ATPsynthase monomer versus dimer profiled by blue native PAGE and activity stain

Studies into the effects of oligomerization on F(0)F(1)ATPsynthase function are contradictory. We optimized the in-gel ATPase assay to investigate the functional differences of monomers versus dimers. In Triton X-100 extracts of heavy bovine heart mitochondria (HBHM) and mitoplasts, but not submitochondrial particles (MgATP-SMP), dimers had greater specific activity than monomers: at 30 degrees C, the dimer/monomer activity ratios were 2.3, 1.4, and 1.0, respectively. These differences in HBHM and mitoplasts extracts were enhanced at 37 degrees C but lost at 20 degrees C. In mitoplasts but not in MgATP-SMP, dimers were selectively shielded from limited chymotrypsin degradation of F(1) alpha subunit, possibly due to interactions with other proteins or ligands in the native inner membrane. Despite these differences, all three preparations had similar percentages of dimers and similar contents of the native inhibitor IF(1) in Vm (monomer) and (dimer) Vd. These results suggest that, in native membrane, monomers and dimers are functionally distinct.     

Some Methods for Calculating Stiffness Properties of Periodic Structures

We present a general numerical method for calculating effective elastic properties of periodic structures based on the homogenization method. Some concrete numerical examples are presented.