Time‐integrated energy domain measurements with synchrotron radiation

A new time integrated method for the study of resonant nuclear scattering of synchrotron radiation in the forward direction or in Bragg directions is introduced. This method gives in principle similar information as the well known time differential method. A brief comparison of both methods is presented. The idea is to excite coherently the nuclei incorporated in two absorbers, one moving with respect to the other. The fields radiated by the nuclei from both absorbers interfere and each time the nuclear energy in one absorber matches, by Doppler modulation, the nuclear energy of the other, an extremum in the time integrated intensity is observed. The results of the first experiments at the Advanced Photon Source at the Argonne National Laboratory will be presented. This revised version was published online in August 2006 with corrections to the Cover Date.     

The completely positive and doubly nonnegative completion problems

We prove the following. Let G be an undirected graph. Every partially specified symmetric matrix, the graph of whose specified entries is G and each of whose fully specified submatrices is completely positive (equal to BB^T for some entrywise nonnegative matrix B), may be completed to a completely positive matrix if and only if G is a block-clique graph (a chordal graph in which distinct maximal cliques overlap in at most one vertex). The same result holds for matrices that are doubly nonnegative (entrywise nonnegative and positive semidefinite).     

An unusual effect of fast neutron irradiation of lanthanide /III/ chlorides

When anhydrous EuCl₃, GdCl₃, DyCl₃ or Eu₂O₃ are irradiated with fast neutrons and then dissolved in dilute hydrochloric acid, small amounts of reducing species, believed to be divalent lanthanide cations, are revealed. The amount produced increases with the thermodynamic stability of the Ln²⁺ species /Eu>Dy>Gd>/.     

Coordinate transform invariance

A four-dimensional operator is shown to contain the operator-generators for rotation, scale, reflections, and boosts. The hypothesis is advanced that a physical system changes under this operator by at most a complex phase factor due to invariance against the choice of menial frame. A canonical transform gives a simple relation between space-time and energy-momentum. The basic conserved quantity is a four-dimensional angular momentum and/or coupling constant. The differential of this function contains a second-order differential product which is constrained as a power series in the independent variable. The analysis explores the consequences of the model and shows its degree of correspondence to the standard models.     

Communication Roles, Perceived Effectiveness, and Satisfaction in an Environmental Management Program

Earlier research has shown a relationship between various forms of structural centrality and perceived leadership and role satisfaction in small experimental groups. The limited amount of research on this topic in naturally occurring social networks has yielded results that often conflict with one another. Different results have generally been attributed to possible differences in task environments. This paper examines the relationship between two types of structural centrality and perceived influence, role satisfaction, and perceived effectiveness in an environmental resource management program. Findings in this paper suggest that the observed differences in relationships between the network and other variables is partly a function of global network properties (e.g., marginality of subgroups) and related task environments. This revised version was published online in August 2006 with corrections to the Cover Date.     

Investigation by EPR and ENDOR spectroscopy of the novel 4Fe ferredoxin fromPyrococcus furiosus

The hyperthermophilic archaeonPyrococcus furiosus contains a four-Fe ferredoxin (Pf- Fd) that differs from most other 4Fe-Fd’s in that its [Fe₄S₄] cluster is anchored to protein by only three cysteinyl residues.Pf- Fd also is of interest because in its reduced form, [Fe₄S₄]⁺, the cluster exhibits bothS = 1/2 andS = 3/2 spin states. Addition of excess cyanide ion converts the cluster exclusively to anS = 1/2 state (g₁ = 2.09, g₂ = 1.95, g₃ = 1.92), however dialysis restores the EPR signal of native reduced protein indicating that the cluster is not irreversibly altered by cyanide. Both the native protein and protein in the presence of excess cyanide ion (Pf- Fd 4Fe-CN) were investigated here using the techniques of electron paramagnetic resonance (EPR) and electron-nuclear double resonance (ENDOR) spectroscopy. In particular,Pf- Fd 4Fe-CN was investigated using¹³CN^? and C¹⁵N^? ligands.¹³C and¹⁵N ENDOR indicated that a single cyanide ion bound directly, with the cluster showing an unusually small contact interaction (a_iso(¹³C)～ ?3 MHz, a_iso(¹⁵N) ～ 0). This is in contrast to cyanide bound to monomeric low-spin Fe(III)-containing proteins such as transferrin and myoglobin, for which the¹³C hyperfine coupling has a large isotropic component (a_iso(¹³C) ≈ ?30 MHz). This small contact interaction is not due to low spin density of Fe, as⁵⁷Fe ENDOR of the singly and triply labeledPf- Fd 4FeCN isotopologs, [⁵⁷FeFe₃S₄]⁺ and [Fe⁵⁷Fe₃S₄]⁺, show hyperfine coupling characteristic for [Fe₄S₄]⁺ clusters, particularly for the Fe to which cyanide binds. Thus, the low spin density on¹³C is not due to low spin density on the Fe ion to which it binds. Further theoretical work is needed to explain the contrast between the strong electronic effect of cyanide ion binding with the low spin density on the ligand.