Development of BNBSL: A ß-ν spectra library for spectrometry applications.

While modern nuclear decay data can provide many details of a given nuclides ß-decay modes (branching ratios, decay heating etc.), knowledge of the emitted ß-energy spectrum is often not included. This limitation hampers the use of decay data in some analysis, such as ß-spectrometry of irradiated material, prediction of ß-decay Bremsstrahlung or antineutrino, ν̄, detection. To address this deficiency, and for increased ease of ß-spectrometry studies of complex samples, a library of ß, ν and Bremsstrahlung-spectra, called BNBSL (Beta-Neutrino-Bremsstrahlung spectra library), has been produced. It has been found that the content compares favourably with experimental data and methodologies for its application to complex nuclear inventories have been developed. BNBSL contains spectra for over 1500 nuclides, which is hoped will benefit applied nuclear, radiation and materials science studies.

Erratum: Sensitivity of (d,p) Reactions to High n-p Momenta and the Consequences for Nuclear Spectroscopy Studies [Phys. Rev. Lett. 117, 162502 (2016)].

This corrects the article DOI: 10.1103/PhysRevLett.117.162502.

Sensitivity of (d, p) Reactions to High n-p Momenta and the Consequences for Nuclear Spectroscopy Studies.

Theoretical models of low-energy (d, p) single-neutron transfer reactions are a crucial link between experimentation, nuclear structure, and nuclear astrophysical studies. Whereas reaction models that use local optical potentials are insensitive to short-range physics in the deuteron, we show that including the inherent nonlocality of the nucleon-target interactions and realistic deuteron wave functions generates significant sensitivity to high n-p relative momenta and to the underlying nucleon-nucleon interaction. We quantify this effect upon the deuteron channel distorting potentials within the framework of the adiabatic deuteron breakup model. The implications for calculated (d, p) cross sections and spectroscopic information deduced from experiments are discussed.

Multiple imaging techniques demonstrate the manipulation of surfaces to reduce bacterial contamination and corrosion.

Surface imaging techniques were combined to determine appropriate manipulation of technologically important surfaces for commercial applications. The complementarity of the microscopy methods, scanning electron microscopy, electron probe microanalysis and atomic force microscopy assessed and correlated form and function of the surface modifications. Stainless steel disks (1 cm in diameter) were laser-cut from the same sheets of stainless steel and treated by electropolishing or left untreated for controls. Each treatment was analysed separately using each technique. First, the disks were examined by visual inspection and electron probe microanalysis for surface characteristics and elemental composition, respectively. Aliquots of bacterial suspensions (saline rinses of poultry carcasses from a commercial broiler processing plant) were then diluted in broth and monitored for growth by spectrophotometry. Stainless steel disks (1 cm in diameter) were added and the cultures were grown to sufficient density to allow attachment of bacterial cells to test surfaces. Relative differences in the surface morphology shown by atomic force microscopy, including Z ranges, roughness and other measurements, corresponded by treatment with the differences in reduction of bacterial counts shown by scanning electron microscopy. A model of wet-processing conditions tested the effects of corrosive treatment of surfaces. Less bacterial attachment occurred after corrosive treatment on controls and electropolished samples. Electropolishing significantly reduced bacterial numbers and the effects of corrosive action compared to the controls. Thus, the multiple imaging techniques showed that engineered changes on stainless steel surfaces improved the resistance of the surface finish to bacterial attachment, biofilm formation, and corrosive action.

Surface finishes on stainless steel reduce bacterial attachment and early biofilm formation: scanning electron and atomic force microscopy study.

Three common finishing treatments of stainless steel that are used for equipment during poultry processing were tested for resistance to bacterial contamination. Methods were developed to measure attached bacteria and to identify factors that make surface finishes susceptible or resistant to bacterial attachment and biofilm formation. Samples of the treated surfaces (sand-blasted, sanded, and electropolished) were exposed to natural bacterial populations from chicken carcass rinses to allow growth of bacteria and development of biofilms on the surfaces. The kinetics of bacterial growth during surface exposure was followed by UV-visible spectrophotometry, and counts of bacteria and early biofilm formation were measured following scanning electron microscopy (SEM). The surface morphology of the samples was analyzed by atomic force microscopy (AFM) with samples from each of the batches of treatments used in the SEM studies. Relative differences in the surface morphology, including fractal dimensions, Z ranges, roughness, and other measurements corresponded by treatment with the differences in reduction of bacterial counts shown by SEM. The surface types varied in affinity for bacteria, and both physical and electrochemical treatments improved resistance of stainless steel to bacterial attachment. Electropolished stainless steel was the least rough surface and showed significantly fewer bacterial cells and beginning biofilm formations than the other treated surfaces. Food safety could be improved if bacterial populations could be reduced during processing by increasing the use of materials that are resistant to bacterial contamination. These findings will aid equipment manufacturers and processors in selecting materials and finishes that are most resistant to bacteria and biofilm formation.

Comparison of child psychiatry residents' and training directors' perceptions of training for alcohol and substance abuse treatment.

Residents anddirectors of accredited child and adolescent psychiatry programs (N = 117) in the United States were surveyed (with a response rate of 89% and 76.9%, respectively) to determine the extent and adequacy of training offered for the identification and management of substance abuse disorders. Of the responders, 24% of the residents indicated some exposure (≥1 hour) to an adolescent drug abuse treatment facility during their training. In contrast, 46% of the directors reported that their residents had such exposure. Residents consistently reported training to be less adequate than did directors. Only half of the residents reported that they felt adequately prepared to identify and initially manage a substance-abusing adolescent, whereas a somewhat higher percentage of the directors (59%) felt that their residents were adequately prepared for this function.

Remobilization of toxic heavy metals adsorbed to bacterial wall-clay composites.

Significant quantities of Ag(I), Cu(II), and Cr(III) were bound to isolated Bacillus subtilis 168 walls, Escherichia coli K-12 envelopes, kaolinite and smectite clays, and the corresponding organic material-clay aggregates (1:1, wt/wt). These sorbed metals were leached with HNO3, Ca(NO3)2, EDTA, fulvic acid, and lysozyme at several concentrations over 48 h at room temperature. The remobilization of the sorbed metals depended on the physical properties of the organic and clay surfaces and on the character and concentration of the leaching agents. In general, the order of remobilization of metals was Cr much less than Ag less than Cu. Cr was very stable in the wall, clay, and composite systems; pH 3.0, 500 microM EDTA, 120-ppm [mg liter-1] fulvic acid, and 160-ppm Ca remobilized less than 32% (wt/wt) of sorbed Cr. Ag (45 to 87%) and Cu (up to 100%) were readily removed by these agents. Although each leaching agent was effective at mobilizing certain metals, elevated Ca or acidic pH produced the greatest overall mobility. The organic chelators were less effective. Lysozyme digestion of Bacillus walls remobilized Cu from walls and Cu-wall-kaolinite composites, but Ag, Cr, and smectite partially inhibited enzyme activity, and the metals remained insoluble. The extent of metal remobilization was not always dependent on increasing concentrations of leaching agents; for example, Ag mobility decreased with some clays and some composites treated with high fulvic acid, EDTA, and lysozyme concentrations. Sometimes the organic material-clay composites reacted in a manner distinctly different from that of their individual counterparts; e.g., 25% less Cu was remobilized from wall- and envelope-smectite composites than from walls, envelopes, or smectite individually in 500 microM EDTA. Alternatively, treatment with 160-ppm Ca removed 1.5 to 10 times more Ag from envelope-kaolinite composites than from the individual components. The particle size of the deposited metal may account for some of the stability changes; those metals that formed large, compact aggregates (Cr and Ag) as seen by transmission electron microscopy were less likely to be remobilized. In summary, it is apparent that remobilization of toxic heavy metals in sediments, soils, and the vadose zone is a complicated issue. Predictions based on single inorganic or organic component systems are too simplistic.

Alcoholism and substance abuse teaching in child psychiatry residency programs.

In order to determine the needs and goals of substance abuse teaching, vis-à-vis child psychiatry training, a questionnaire was sent to the training directors at every child psychiatry program accredited by the Accreditation Council of Graduate Medical Examination. The results demonstrated that most child psychiatry programs schedule at least some didactic time specifically for substance abuse topics. However, only 59% of the training directors felt that their fellows were adequately educated to identify and at least initially manage a drug abusing adolescent.

Bacterial sorption of heavy metals.

Four bacteria, Bacillus cereus, B. subtilis, Escherichia coli, and Pseudomonas aeruginosa, were examined for the ability to remove Ag+, Cd2+, Cu2+, and La3+ from solution by batch equilibration methods. Cd and Cu sorption over the concentration range 0.001 to 1 mM was described by Freundlich isotherms. At 1 mM concentrations of both Cd2+ and Cu2+, P. aeruginosa and B. cereus were the most and least efficient at metal removal, respectively. Freundlich K constants indicated that E. coli was most efficient at Cd2+ removal and B. subtilis removed the most Cu2+. Removal of Ag+ from solution by bacteria was very efficient; an average of 89% of the total Ag+ was removed from the 1 mM solution, while only 12, 29, and 27% of the total Cd2+, Cu2+, and La3+, respectively, were sorbed from 1 mM solutions. Electron microscopy indicated that La3+ accumulated at the cell surface as needlelike, crystalline precipitates. Silver precipitated as discrete colloidal aggregates at the cell surface and occasionally in the cytoplasm. Neither Cd2+ nor Cu2+ provided enough electron scattering to identify the location of sorption. The affinity series for bacterial removal of these metals decreased in the order Ag greater than La greater than Cu greater than Cd. The results indicate that bacterial cells are capable of binding large quantities of different metals. Adsorption equations may be useful for describing bacterium-metal interactions with metals such as Cd and Cu; however, this approach may not be adequate when precipitation of metals occurs.

Physicochemical interaction of Escherichia coli cell envelopes and Bacillus subtilis cell walls with two clays and ability of the composite to immobilize heavy metals from solution.

Isolated Escherichia coli K-12 cell envelopes or Bacillus subtilis 168 cell walls were reacted with smectite or kaolinite clay in distilled deionized water (pH 6.0); unbound envelopes or walls were separated by sucrose density gradient centrifugation, and the extent of adsorption was calculated. At saturation, both clays adsorbed approximately 1.0 mg (dry weight) of envelopes or walls per mg (dry weight) of clay. Clays showed a preference for edge-on orientation with both walls and envelopes, which was indicative of an aluminum polynuclear bridging mechanism between the wall or envelope surface and the clay edge. The addition of heavy metals increased the incidence of planar surface orientations, which suggested that multivalent metal cation bridging was coming into play and was of increasing importance. The metal-binding capacity of isolated envelopes, walls, clays, and envelope-clay or wall-clay mixtures was determined by atomic absorption spectroscopy after exposure to aqueous 5.0 mM Ag+, Cu2+, Cd2+, Ni2+, Pb2+, Zn2+, and Cr3+ nitrate salt solutions at pHs determined by the buffering capacity of wall, envelope, clay, or composite system. The order of metal uptake was walls greater than envelopes greater than smectite clay greater than kaolinite clay for the individual components, and walls plus smectite greater than walls plus kaolinite greater than envelopes plus smectite greater than envelopes plus kaolinite for the mixtures. On a dry-weight basis, the envelope-clay and wall-clay mixtures bound 20 to 90% less metal than equal amounts of the individual components did.(ABSTRACT TRUNCATED AT 250 WORDS)

Current perspectives on substance abuse in youth.

The literature on substance abuse in youth is reviewed and current terminology is defined. Perspectives are presented on epidemiology, etiology, diagnosis and differential diagnosis, prevention, treatment, outcome, associated problems, issues of interface with other professionals, and directions for future research. Substance abuse in children and adolescents is a major public health problem. The definitive cause is unknown; there is a progression from legal to illegal drugs. Prevention methods are most effectively aimed at stopping initial use, and treatment remains variable. Child and adolescent psychiatrists are encouraged to become more involved in the problem.

Competitive hydration of quinazoline at the montmorillonite-water interface.

Ultraviolet spectroscopic analyses of suspensions of quinazoline and Na(+)-saturated montmorillonite have indicated that covalent hydration of the monovalent organic cation is inhibited at or near the clay surface. A similar lack of hydration was observed in solutions of quinazoline and high-ionic-strength calcium chloride. The inhibition is attributed to a local competition between quinazoline and the inorganic cations for water of hydration.