Critical Literacy in the Social Studies Classroom: A Case for the 21st Century

This article considers the potential of integrating critical literacy into approaches to teaching and learning social studies as an indispensable tool for building better communities (Agbaria, 2011). It begins with an overview of the authors’ experiences and perspectives related to social studies and critical literacy. It then proceeds to consider current perceptions and practices regarding literacy in U.S. classrooms and the trend towards teaching and learning literacy and a distinct set of technical and functional knowledge and skills that are often taught in isolation. The article then examines conceptions of critical literacy and considers connections to social studies education. Finally, it considers how critical approaches to teaching and learning literacy and social studies might be united to promote and support the development of critical thinking skills necessary for today’s students to successfully address issues in an increasingly complex and interconnected global society

Thermophysical properties of the lanthanide sesquisulfides. III. Determination of Schottky and lattice heat‐capacity contributions of γ‐phase Sm2S3 and evaluation of the thermophysical properties of the γ‐phase Ln2S3 subset

We report the experimental heat capacity of γ‐phase Sm2S3 and derived thermophysical properties at selected temperatures. The entropy, enthalpy increments, and Gibbs energy function are 21.50R, 3063R⋅K, and 11.23R at 298.15 K. The experimental heat capacity is made up of lattice and electronic (Schottky) contributions. The lattice contribution is determined for all γ‐phase lanthanide sesquisulfides (Ln2S3 ) using the Komada/Westrum model. The difference between the experimental heat capacity and the deduced lattice heat capacity is analyzed as the Schottky contribution. Comparisons are made between the calorimetric Schottky contributions and those determined based on crystal‐field electronic energy levels of Ln3+ ions in the lattice and between the Schottky contributions obtained from the empirical volumetric priority approach and from the Komada/Westrum theoretical approach. Predictions for the thermophysical properties of γ‐phase Eu2S3 and γ‐phase Pm2S3 (unavailable for experimental determination) are also presented.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/71137/2/JCPSA6-96-8-6149-1.pd

Thermophysical properties of the lanthanide sesquisulfides. IV. Schottky contributions, magnetic, and electronic properties of ϵ‐phase Yb2S3 and Lu2S3

The heat capacities of ϵ‐phase Yb2S3 and Lu2S3 have been determined from 6 to 350 K and their thermodynamic properties evaluated. The resolution of the Schottky and magnetic properties by evaluation of the lattice heat capacity is shown to be in accord with spectroscopically determined energy levels. The lattice heat capacity of Yb2S3 was determined by means of the Komada–Westrum phonon distribution model. Excess heat‐capacity contributions were thus evaluated and analyzed as Schottky and magnetic heat capacities. A phase transition associated with magnetic ordering was detected in the heat capacity of Yb2S3 near 7 K with an entropy content of 0.68R. The entropies at 298.15 K are 22.77R and 19.74R for Yb2S3 and for Lu2S3.  Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/70016/2/JCPSA6-98-2-1458-1.pd

Thermophysical properties of the lanthanide sesquisulfides. II. Schottky contributions and magnetic and electronic properties of γ‐phase Pr2S3, Tb2S3, and Dy2S3

Heat‐capacity measurements by adiabatic equilibrium calorimetry are reported for γ‐phase Pr2S3, Tb2S3, and Dy2S3 between 5 and 350 K. Highly purified samples were prepared and their composition verified by chemical analysis. Precision lattice parameters were determined for each compound and are compared with literature values. The total heat capacity has been resolved into lattice, magnetic, and Schottky components by a volumetric approach. The experimental Schottky contributions accord with the calculated curves based on the crystal‐field splitting of the 2S+1LJ ground state of the lanthanide ions occupying sites of S4 symmetry in the Th3P4 lattice. The individual crystal‐field electronic energy levels have been obtained in part from an analysis of the hot‐band data observed in the absorption spectra of Pr2S3, Tb2S3, and Dy2S3, and from a calculated splitting in which the crystal‐field parameters Bkm, were determined from a lattice‐sum calculation. Molar thermodynamic properties are reported for all three compounds. The entropy at 298.15 K {S0−S0 (7 K)}, is 22.78R, 22.93R, and 23.36R, for γ‐phase Pr2S3, Tb2S3, and Dy2S3, respectively.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/70592/2/JCPSA6-95-3-1964-1.pd

Validation of a new automatic smoking machine to study the effects of cigarette smoke in newborn lambs

The aim of this study was to describe the characteristics and validate the use of a new, custom-built automatic smoking machine (ASM), primarily designed to study the effects of an environmental tobacco smoke surrogate (ETS surrogate) exposure in animals of various sizes, including large animals. The equipment includes a programmable ASM coupled to a vented whole body chamber, where animals can be exposed to both mainstream and sidestream smoke. The user-friendly interface allows for full programming of puff volume (1-60 mL), time interval between two puffs (1-60 s) and between two cigarettes (1-60 min). Eight newborn lambs were exposed to either 10 (4 lambs, C10 group) or 20 (4 lambs, C20 group) cigarettes, 8 h per day for 15 days. Four additional control, lambs were exposed to air (C0 group). Weight gain was identical in all three groups of lambs. Urinary cotinine/creatinine ratio increased with the number of cigarettes smoked (C0: 11 ± 7 ng/mg; C10: 961 ± 539 ng/mg; C20: 1821 ± 312 ng/mg), with levels in the C10 and C20 groups in keeping with values published in infants exposed to ETS. Overall, results show that our new ASM is especially well suited for ETS surrogate exposure in non-restrained, non-anaesthetized large animals such as sheep

A Modern Mode of Activation for Nucleic Acid Enzymes

Through evolution, enzymes have developed subtle modes of activation in order to ensure the sufficiently high substrate specificity required by modern cellular metabolism. One of these modes is the use of a target-dependent module (i.e. a docking domain) such as those found in signalling kinases. Upon the binding of the target to a docking domain, the substrate is positioned within the catalytic site. The prodomain acts as a target-dependent module switching the kinase from an off state to an on state. As compared to the allosteric mode of activation, there is no need for the presence of a third partner. None of the ribozymes discovered to date have such a mode of activation, nor does any other known RNA. Starting from a specific on/off adaptor for the hepatitis delta virus ribozyme, that differs but has a mechanism reminiscent of this signalling kinase, we have adapted this mode of activation, using the techniques of molecular engineering, to both catalytic RNAs and DNAs exhibiting various activities. Specifically, we adapted three cleaving ribozymes (hepatitis delta virus, hammerhead and hairpin ribozymes), a cleaving 10-23 deoxyribozyme, a ligating hairpin ribozyme and an artificially selected capping ribozyme. In each case, there was a significant gain in terms of substrate specificity. Even if this mode of control is unreported for natural catalytic nucleic acids, its use needs not be limited to proteinous enzymes. We suggest that the complexity of the modern cellular metabolism might have been an important selective pressure in this evolutionary process

Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study

<p>Abstract</p> <p>Background</p> <p>To better characterize the value of cerebrospinal fluid (CSF) proteins as diagnostic markers in a clinical population of subacute encephalopathy patients with relatively low prevalence of sporadic Creutzfeldt-Jakob disease (sCJD), we studied the diagnostic accuracies of several such markers (14-3-3, tau and S100B) in 1000 prospectively and sequentially recruited Canadian patients with clinically suspected sCJD.</p> <p>Methods</p> <p>The study included 127 patients with autopsy-confirmed sCJD (prevalence = 12.7%) and 873 with probable non-CJD diagnoses. Standard statistical measures of diagnostic accuracy were employed, including sensitivity (Se), specificity (Sp), predictive values (PVs), likelihood ratios (LRs), and Receiver Operating Characteristic (ROC) analysis.</p> <p>Results</p> <p>At optimal cutoff thresholds (empirically selected for 14-3-3, assayed by immunoblot; 976 pg/mL for tau and 2.5 ng/mL for S100B, both assayed by ELISA), Se and Sp respectively were 0.88 (95% CI, 0.81-0.93) and 0.72 (0.69-0.75) for 14-3-3; 0.91 (0.84-0.95) and 0.88 (0.85-0.90) for tau; and 0.87 (0.80-0.92) and 0.87 (0.84-0.89) for S100B. The observed differences in Sp between 14-3-3 and either of the other 2 markers were statistically significant. Positive LRs were 3.1 (2.8-3.6) for 14-3-3; 7.4 (6.9-7.8) for tau; and 6.6 (6.1-7.1) for S100B. Negative LRs were 0.16 (0.10-0.26) for 14-3-3; 0.10 (0.06-0.20) for tau; and 0.15 (0.09-0.20) for S100B. Estimates of areas under ROC curves were 0.947 (0.931-0.961) for tau and 0.908 (0.888-0.926) for S100B. Use of interval LRs (iLRs) significantly enhanced accuracy for patient subsets [<it>e.g</it>., 41/120 (34.2%) of tested sCJD patients displayed tau levels > 10,000 pg/mL, with an iLR of 56.4 (22.8-140.0)], as did combining tau and S100B [<it>e.g</it>., for tau > 976 pg/mL and S100B > 2.5 ng/mL, positive LR = 18.0 (12.9-25.0) and negative LR = 0.02 (0.01-0.09)].</p> <p>Conclusions</p> <p>CSF 14-3-3, tau and S100B proteins are useful diagnostic markers of sCJD even in a low-prevalence clinical population. CSF tau showed better overall diagnostic accuracy than 14-3-3 or S100B. Reporting of quantitative assay results and combining tau with S100B could enhance case definitions used in diagnosis and surveillance of sCJD.</p