Microscale functional group analysis of marine and sedimentary humic substances

Methods are described for the microscale analysis of aquatic and sedimentary humic substances for several oxygen-containing functional groups including total acidity, carboxylic and phenolic hydroxyl groups, quinone groups and hydroxamate linkages. Coefficients of variation of the methods range from 4.9 to 12.9%.     

The spectrophotometric determination of microgram amounts of cerium

A spectrophotometric procedure, which has a coefficient of variation of ca. 2%, is described for the determination of up to 80 μg of cerium. Ceric ion formed by oxidation with persulphate, in the presence of catalytic amounts of silver, is reduced to the cerous state by treatment with excess ferrous-phenanthroline reagent. The decrease in optical density of the ferrous-phenan-throline compared with the reagent blank is a measure of the amount of cerium present. The only common cations which cause serious interference are Mn⁺²and Cr⁺³.     

Neutron spectra at 0° from (p,n) reactions on 9Be, 12C,and 27Al at 647 and 800 MeV

The measured cross sections show a narrow high-energy peak (20–30 MeV/cFWHM) and a broad bump at lower momenta associated with pion production. Comparison is made to an intranuclear cascade calculation.     

The determination of technetium-99 in seawater and marine algae

Technetium-99 is preconcentrated from acidified seawater containing a trace of bromine by adsorbing it as the pertechnetate ion on the anion exchanger Duolite A101D. After elution with 4 M nitric acid, it is purified from other radionuclides by scavenging with hydrous iron(III) oxide and extracting from 5 M sodium hydroxide medium into methyl ethyl ketone. The organic phase is then evaporated and technetium is electrodeposited from oxalic acid medium onto a bronze disc and counted with a low background β-counter. Overall recovery is > 90% and the precision is ±0.2 pCi l^-1 at a technetium level of 0.6–1.0 pCi l^-1. Concentrations of the radionuclide in the central Irish Sea were found to lie in the range 0.4–2 pCi l^-1. The same analytical scheme can be used for determining the element in nitric acid digests of marine algae.     

Dielectron widths of the Gamma(1S,2S,3S) resonances

We determine the dielectron widths of the Gamma(1S), Gamma(2S), and Gamma(3S) resonances with better than 2% precision by integrating the cross section of e+e- -->Gamma over the e+e- center-of-mass energy. Using e+e- energy scans of the Gamma resonances at the Cornell Electron Storage Ring and measuring Gamma production with the CLEO detector, we find dielectron widths of 1.252+/-0.004(sigma(stat))+/-0.019(sigma(syst)) keV, 0.581+/-0.004+/-0.009 keV, and 0.413+/-0.004+/-0.006 keV for the Gamma(1S), Gamma(2S), and Gamma(3S), respectively.     

Observation of psi(3770) --> pi pi J/psi and measurement of Gamma ee[psi(2S)

We observe signals for the decays psi(3770) --> XJ/psi from data acquired with the CLEO detector operating at the CESR e+ e- collider with square root of s = 3773 MeV. We measure the following branching fractions Beta(psi(3770) --> XJ/psi and significances: (189 +/- 20 +/- 20) x 10(-5) (11.6sigma) for X = pi+ pi-, (80 +/- 25 +/- 16) x 10(-5) (3.4sigma) for X = pi0 pi0, and (87 +/- 33 +/- 22) x 10(-5) (3.5sigma) for X = eta, where the errors are statistical and systematic, respectively. The radiative return process e+ e- --> gamma psi(2S) populates the same event sample and is used to measure Gamma ee[psi(2S)] = (2.54 +/- 0.03 +/- 0.11) keV.     

Experimental limits on weak annihilation contributions to decays

We present the first experimental limits on high-q2 contributions to charmless semileptonic decays of the form expected from the weak annihilation (WA) decay mechanism. Such contributions could bias determinations of /Vub/ from inclusive measurements of B-->Xulupsilon. Using a wide range of models based on available theoretical input we set a limit of GammaWA/Gammab-->u<7.4% (90% confidence level) on the WA fraction, and assess the impact on previous inclusive determinations of /Vub/.     

A typological analysis: understanding pre-service teacher beliefs and how they are transformed

This article describes the beliefs and their transformations of members of a cohort of early-childhood, elementary and middle-level pre-service teachers (PSTs) as they professionally develop. A typological analysis of both quantitative and qualitative data collected between August 2011 and May 2013 was utilized to categorize how 40 PSTs’ beliefs transformed throughout their formal teacher preparation. Five typologies were identified, showing variation in how PST beliefs transform or remain static.

Among the findings, strong support related to the development of innovative beliefs during coursework coupled with at least one transformative experience where innovation was observed ‘working’ in the field were sufficient for the transformation to innovative beliefs, despite potential constraints by supervisors, cooperating teachers and/or mandated curricula (Typology 3). Another finding revealed disguised growth toward innovation among those in Typology 5, who reported being innovative and having productive beliefs but described extremely traditional practices. Implications call for improved connections between mathematics methods professors and field supervisors, particularly during clinical internships when PSTs are no longer enrolled in methods courses, to enhance PSTs’ productive struggle in their development of innovative beliefs (T3) and to increase opportunities for disconnects between innovative beliefs and traditional practices to be made explicit and negotiated (T5).     

Role of solvation in the energy stabilization inside the hydrophobic core of the protein rubredoxin

There are many forces that contribute to the stability of a protein; among these are dispersion interactions, hydrogen bonding, and solvation effects. In a recent work, Vondrasek et al. estimated the in vacuo stabilization energy of the hydrophobic core of the protein rubredoxin using high level ab initio methods (Vondrasek, J.; et al. J. Am. Chem. Soc. 2005, 127, 2615). In this work, we evaluate the effects of solvation on the stability of the hydrophobic core of this protein. Solvation calculations are made using the polarizable continuum method at the MP2/aug-cc-pVDZ level of theory. It is found that, in a protein-like environment (mimicked by a continuum solvent with a dielectric constant of approximately 4), the stability of rubredoxin's hydrophobic core is decreased by 40-50%. We also observed that the stabilization energy of the hydrophobic core is only slightly lower in a protein-like medium than in an aqueous one (DeltaGether-DeltaGwater approximately 1.0-3.5 kcal/mol).     

Lie superalgebras whose enveloping algebras satisfy a non-matrix polynomial identity

Let L be a Lie superalgebra with its enveloping algebra U(L) over a field F. A polynomial identity is called non-matrix if it is not satisfied by the algebra of 2×2 matrices over F. We characterize L when U(L) satisfies a non-matrix polynomial identity. We also characterize L when U(L) is Lie solvable, Lie nilpotent, or Lie super-nilpotent.