Research and Teacher Education: The BERA-RSA inquiry. Policy and Practice within the United Kingdom.

Across the four jurisdictions of the United Kingdom (England, Northern Ireland, Scotland and Wales) initial teacher education (ITE) is under active development, with its content, location, control and quality often the focuses of sustained debate. Statutory and professional requirements for the sector inevitably reflect differing assumptions about teaching, teacher knowledge and governance. In exploring ITE across the four jurisdictions, this paper reviews policies and practices through two major focuses: first, the relationships between the declared teacher standards (competencies/competences) and research-informed teacher education provision; second, the ‘turn or (re)turn to the practical’ in teacher education, including policy declarations, changes in practices, and emphases and effects of the discourse(s) of relevance

Simple pressure gauge for uranium hexafluoride

A sensitive detector and pressure gauge for uranium hexafluoride in high‐vacuum systems is described. Negative surface ionization of UF_6 occurs on ribbon filaments operated at temperatures too low for electron emission to be significant. The ion current measured on a cylindrical collector surrounding the filament assembly varies regularly with UF_6 pressure below 10^(−3) Torr. Different filament materials are considered, including rhenium, thoriated tungsten, and platinum. Rhenium is found to be the most satisfactory material for operation of diode emitters as a pressure gauge. Gauge constants (in A Torr^(−1)) are derived from comparing negative surface ionization currents with the response of a capacitance manometer and are shown to be independent of temperature within a reasonable operating range. The effects of exposing the rhenium filament to various gases is considered, and it is shown that brief exposure to acetylene substantially improves the operating characteristics of the gauge

\u3cem\u3eDrosophila\u3c/em\u3e Vitelline Membrane Assembly: A Critical Role for an Evolutionarily Conserved Cysteine in the “VM domain” of sV23

The vitelline membrane (VM), the oocyte proximal layer of the Drosophila eggshell, contains four major proteins (VMPs) that possess a highly conserved “VM domain” which includes three precisely spaced, evolutionarily conserved, cysteines (CX7CX8C). Focusing on sV23, this study showed that the three cysteines are not functionally equivalent. While substitution mutations at the first (C123S) or third (C140S) cysteines were tolerated, females with a substitution at the second position (C131S) were sterile. Fractionation studies showed that sV23 incorporates into a large disulfide linked network well after its secretion ceases, suggesting that post-depositional mechanisms are in place to restrict disulfide bond formation until late oogenesis, when the oocyte no longer experiences large volume increases. Affinity chromatography utilizing histidine tagged sV23 alleles revealed small sV23 disulfide linked complexes during the early stages of eggshell formation that included other VMPs, namely sV17 and Vml. The early presence but late loss of these associations in an sV23 double cysteine mutant suggests that reorganization of disulfide bonds may underlie the regulated growth of disulfide linked networks in the vitelline membrane. Found within the context of a putative thioredoxin active site (CXXS) C131, the critical cysteine in sV23, may play an important enzymatic role in isomerizing intermolecular disulfide bonds during eggshell assembly

Dissociative electron attachment reactions of transition metal carbonyls and their apparent influence on the thermalization of electrons by CO2

Dissociative electron attachment rates are measured for the transition metal carbonyls V(CO)6, Cr(CO)6, Fe(CO)5, Ni(CO)4, Mo(CO)6, and W(CO)6. Rates are measured as a function of the pressure of CO2 added to relax epithermal electrons. Derived thermal rate constants for the formation of M(CO)-n-1 from M(CO)n are 0.6, 3.0, 2.0, 2.0, 1.3, and 1.2×10^−7 cm3 molecule−1 s−1, respectively. The differences in these rate constants may be attributed to the different stabilities of the molecular anion with regard to dissociation versus autodetachment. The measured rate of thermalization of electrons by CO2 varies with the metal carbonyl used and depends on the variation of the dissociative electron capture cross section with electron energy. Each system is thus tightly coupled in that the electron energy distribution is determined not only by collisional processes involving CO2 but varies as well with the energy dependent depletion of the distribution by reactant species

Ion cyclotron resonance studies of radiative and dissociative electron attachment processes at low pressures

Ion cyclotron resonance spectroscopy is used to measure nondissociative electron attachment rate constants for C6F6 (perfluorobenzene), C7F8 (perfluorotoluene), c-C4F8 (perfluorocyclobutane), and C7F14 (perfluoromethylcyclohexane) at low pressure (<10−6 Torr). Infrared emission is assumed to stabilize excited species leading to long-lived molecular negative ions. Combining the present data with negative ion lifetimes measured at low pressures by time-of-flight methods and electron attachment rates measured at high pressures in swarm experiments allows estimates of radiative lifetimes to be made. These all fall in the range from 0.4 to 1.5 msec, which are typical of infrared radiative lifetimes. Data are also presented for dissociative electron attachment to CCl4, where the rate limiting step is shown to be thermalization of the electron energy distribution. A number of different buffer gases are examined and the ion cyclotron resonance results extrapolate to yield the attachment rate measured in high pressure swarm experiments

Cholesterol provides nonsacrificial protection of membrane lipids from chemical damage at air–water interface

The role of cholesterol in bilayer and monolayer lipid membranes has been of great interest. On the biophysical front, cholesterol significantly increases the order of the lipid packing, lowers the membrane permeability, and maintains membrane fluidity by forming liquid-ordered–phase lipid rafts. However, direct observation of any influence on membrane chemistry related to these cholesterol-induced physical properties has been absent. Here we report that the addition of 30 mol % cholesterol to 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) or 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1′-rac-glycerol) (POPG) monolayers at the air–water interface greatly reduces the oxidation and ester linkage cleavage chemistries initiated by potent chemicals such as OH radicals and HCl vapor, respectively. These results shed light on the indispensable chemoprotective function of cholesterol in lipid membranes. Another significant finding is that OH oxidation of unsaturated lipids generates Criegee intermediate, which is an important radical involved in many atmospheric processes

Vortex Plastic Flow, B(x,y,H(t)),M(H(t)),Jc(B(t))B(x,y,H(t)), M(H(t)), J_c(B(t)), Deep in the Bose Glass and Mott-Insulator Regimes

We present simulations of flux-gradient-driven superconducting vortices interacting with strong columnar pinning defects as an external field $H(t)$ is quasi-statically swept from zero through a matching field $B_{\phi}$. We analyze several measurable quantities, including the local flux density $B(x,y,H(t))$, magnetization $M(H(t))$, critical current $J_{c}(B(t))$, and the individual vortex flow paths. We find a significant change in the behavior of these quantities as the local flux density crosses $B_{\phi}$, and quantify it for many microscopic pinning parameters. Further, we find that for a given pin density $J_c(B)$ can be enhanced by maximizing the distance between the pins for $B < B_{\phi}$.Comment: 4 pages, 4 PostScript Figure

Time Resolved Study of Hydroxyl Radical Oxidation of Oleic Acid at the Air-Water Interface

The ubiquity of oleic acid (OA) renders it a poster child for laboratory investigations of environmental oxidation chemistry. In the current study, mechanistic details of the oxidation of OA by hydroxyl radicals at the air-water interface are investigated using field-induced droplet ionization mass spectrometry (FIDI-MS). Products from OH oxidation of both unsaturated and saturated carbon atoms are identified, and mechanisms for both types of oxidation processes are proposed. Uptake of oxygen in the interfacial layer increases linearly with time, consistent with Langmuir-Hinshelwood reaction kinetics. These results provide fundamental knowledge relating to OH initiated degradation of fatty acids in atmospheric aerosols

Revisiting the theoretical DBV (V777 Her) instability strip: the MLT theory of convection

We reexamine the theoretical instability domain of pulsating DB white dwarfs (DBV or V777 Her variables). We performed an extensive $g$-mode nonadiabatic pulsation analysis of DB evolutionary models considering a wide range of stellar masses, for which the complete evolutionary stages of their progenitors from the ZAMS, through the thermally pulsing AGB and born-again phases, the domain of the PG1159 stars, the hot phase of DO white dwarfs, and then the DB white dwarf stage have been considered. We explicitly account for the evolution of the chemical abundance distribution due to time-dependent chemical diffusion processes. We examine the impact of the different prescriptions of the MLT theory of convection and the effects of small amounts of H in the almost He-pure atmospheres of DB stars on the precise location of the theoretical blue edge of the DBV instability strip.Comment: Proceedings, 16th European White Dwarf Workshop, Barcelona, 200