El error 'rectificación' en la dislexia.

Analizar el error 'rectificación'en la lectura oral teniendo en cuentas tres variables: niveles, pruebas y sexo; por separado e interrelacionadas cuando ha sido posible. 411 alumnos: 130 alumnos de segundo nivel, 133 de tercer nivel y 148 de cuarto nivel, pertenecientes a 30 centros de Ávila, León, Madrid, Zamora, Valladolid, Salamanca y Burgos. Trabajo surgido a raíz de la multitud de estudios sobre la dislexia han surgido diversas denominaciones y causas de la misma que están expuestas en la primer parte del trabajo. La segunda parte refleja una larga investigación: la base de la misma ha sido el T.A.L.E. ( Test de lecto-escritura) y su aplicación en una determinada muestra de individuos, de donde han sido extraídos los datos necesarios para analizar el error 'rectificación' (uno de los baremados en la prueba de lectura oral de que consta el TALE; por lo tanto la segunda parte de este trabajo ha sido puramente práctica. 1) El error 'rectificación' es en relación a los demás, medianamente frecuente. Es preciso señalar que la frecuencia sólo se puede observar en relación a cada prueba; pues cada una costa de un número determinado de errores. 2) En general, el error 'retificación' es bastante más frecuente en los hombres que en las mujeres. 3) No se da un aumento de frecuencia, a medida que se avanza de nivel, tanto en la prueba de las sílabas cómo en las palabras; la de texto no puede ser incluida en esta comparación puesto que cada curso tiene un texto concreto. 4) En la prueba de sílabas, y en los hombres, no existe una disminución progresiva de fallos respecto al aumento de nivel; y en las mujeres tampoco. 5) En la prueba de palabras y en los hombres si se da una disminución progresiva de porcentajes a medida que se avanza de nivel; no sucediendo lo mismo en las mujeres. 6) Las palabras de mayor porcentaje, sin distinción de sexo, son: gitano, corona, clavel, rastapi, opasto y anglicano.

El error de sustitución simple en la lectura oral.

Análisis escolar de errores que cometen los niños al leer, con que frecuencia, en que etapa escolar y en que tipo de sílaba y palabra. 411 alumnos de segundo, tercero y cuarto cuyo dominio de la lectura sea claramante inferior al que debería tener dado el curso en que están. No incluye a los niños de bajo nivel intelectual, con carácter neurológico o psicopatológico, que no tuvieran como lengua materna el español o procediesen de hogares bilingües etc.. Analizar la frecuencia de errores de sustitución simple en la lectura oral de sílabas, palabras, teniendo en cuenta el nivel escolar de los sujetos, el sexo, el tipo de sílabas, la acentuación y tipo de palabras. El test elaborado por TORO y CERVERA : el test T.A.L.E. (test de análisisde lectoescritura). Subtest de lectura consta de dos series de pruebas de las cuales una sirve para evaluar la eficacia en lectura oral y la otra para la comprobación de la eficacia en lectura silenciosa; y subtest de escritura con pruebas de copia, dictado, escritura espontánea. Teniendo en cuenta el nivel escolar se ha observado que conforme aumenta el grado o nivel escolar, los sujetos cometen menos errores, es obvia la disminución progresiva de errores. Las mujeres cometen más errores que los hombres, pero esta diferencia no es muy signifaicativa considerando la existencia de otras conclusiones, donde las afirmaciones son contrarias (que los hombres cometen más errores). Con respecto a los criterios de acentuación y tipos de palabras se cometen más errores en las palabras agudas y en las polisílabas que en las monosílabas. La importacia de la influencia de la enseñanza de la lectura y su progresiva exigencia. No hay una diferencia apreciable entre el rendimiento en lectura en los varones y el las mujeres aunque muchos autores afirman que el sexo masculino tiene más dificultades.

Variabilidad interobservador : analizando algunas fuentes de error : heurísticas y categorizaciones.

Monográfico con el título: 'La Docencia en Ciencias de la Salud'. Resumen basado en el de la publicación

??Error u horror? : la importancia del error en la clase de ELE

Resumen basado en el de la publicaci??n

Usos del error en la ense??anza de las matem??ticas

Resumen basado en el de la publicaci??n

A la caza del error : una actividad para aprender ortograf??a en las redes sociales

Monogr??fico con el t??tulo: Las redes sociales como herramienta para la ense??anza de la lengua y la literatura

Error and complexity of random walk Monte Carlo radiosity

The author studies the error and complexity of the discrete random walk Monte Carlo technique for radiosity, using both the shooting and gathering methods. The author shows that the shooting method exhibits a lower complexity than the gathering one, and under some constraints, it has a linear complexity. This is an improvement over a previous result that pointed to an O(n log n) complexity. The author gives and compares three unbiased estimators for each method, and obtains closed forms and bounds for their variances. The author also bounds the expected value of the mean square error (MSE). Some of the results obtained are also shown

Selected configuration interaction with truncation energy error and application to the Ne atom

Selected configuration interaction (SCI) for atomic and molecular electronic structure calculations is reformulated in a general framework encompassing all CI methods. The linked cluster expansion is used as an intermediate device to approximate CI coefficients BK of disconnected configurations (those that can be expressed as products of combinations of singly and doubly excited ones) in terms of CI coefficients of lower-excited configurations where each K is a linear combination of configuration-state-functions (CSFs) over all degenerate elements of K. Disconnected configurations up to sextuply excited ones are selected by Brown's energy formula, ΔEK=(E-HKK)BK2/(1-BK2), with BK determined from coefficients of singly and doubly excited configurations. The truncation energy error from disconnected configurations, Δdis, is approximated by the sum of ΔEKS of all discarded Ks. The remaining (connected) configurations are selected by thresholds based on natural orbital concepts. Given a model CI space M, a usual upper bound ES is computed by CI in a selected space S, and EM=E S+ΔEdis+δE, where δE is a residual error which can be calculated by well-defined sensitivity analyses. An SCI calculation on Ne ground state featuring 1077 orbitals is presented. Convergence to within near spectroscopic accuracy (0.5 cm-1) is achieved in a model space M of 1.4× 109 CSFs (1.1 × 1012 determinants) containing up to quadruply excited CSFs. Accurate energy contributions of quintuples and sextuples in a model space of 6.5 × 1012 CSFs are obtained. The impact of SCI on various orbital methods is discussed. Since ΔEdis can readily be calculated for very large basis sets without the need of a CI calculation, it can be used to estimate the orbital basis incompleteness error. A method for precise and efficient evaluation of ES is taken up in a companion paper

Basis set superposition error-counterpoise corrected potential energy surfaces : application to hydrogen peroxide ... X (X=F-, Cl-, Br-, Li+, Na+) complexes

Møller-Plesset (MP2) and Becke-3-Lee-Yang-Parr (B3LYP) calculations have been used to compare the geometrical parameters, hydrogen-bonding properties, vibrational frequencies and relative energies for several X- and X+ hydrogen peroxide complexes. The geometries and interaction energies were corrected for the basis set superposition error (BSSE) in all the complexes (1-5), using the full counterpoise method, yielding small BSSE values for the 6-311 + G(3df,2p) basis set used. The interaction energies calculated ranged from medium to strong hydrogen-bonding systems (1-3) and strong electrostatic interactions (4 and 5). The molecular interactions have been characterized using the atoms in molecules theory (AIM), and by the analysis of the vibrational frequencies. The minima on the BSSE-counterpoise corrected potential-energy surface (PES) have been determined as described by S. Simón, M. Duran, and J. J. Dannenberg, and the results were compared with the uncorrected PES

A chemical Hamiltonian approach study of the basis set superposition error changes on electron densities and one- and two-center energy components

A comparision of the local effects of the basis set superposition error (BSSE) on the electron densities and energy components of three representative H-bonded complexes was carried out. The electron densities were obtained with Hartee-Fock and density functional theory versions of the chemical Hamiltonian approach (CHA) methodology. It was shown that the effects of the BSSE were common for all complexes studied. The electron density difference maps and the chemical energy component analysis (CECA) analysis confirmed that the local effects of the BSSE were different when diffuse functions were present in the calculations

Effect of basis set superposition error on the electron density of molecular complexes

The effect of basis set superposition error (BSSE) on molecular complexes is analyzed. The BSSE causes artificial delocalizations which modify the first order electron density. The mechanism of this effect is assessed for the hydrogen fluoride dimer with several basis sets. The BSSE-corrected first-order electron density is obtained using the chemical Hamiltonian approach versions of the Roothaan and Kohn-Sham equations. The corrected densities are compared to uncorrected densities based on the charge density critical points. Contour difference maps between BSSE-corrected and uncorrected densities on the molecular plane are also plotted to gain insight into the effects of BSSE correction on the electron density

Second-order Møller-Plesset perturbation theory without basis set superposition error : II : open-shell systems

The basis set superposition error-free second-order MØller-Plesset perturbation theory of intermolecular interactions was studied. The difficulties of the counterpoise (CP) correction in open-shell systems were also discussed. The calculations were performed by a program which was used for testing the new variants of the theory. It was shown that the CP correction for the diabatic surfaces should be preferred to the adiabatic ones

C-H···O H-bonded complexes: how does basis set superposition error change their potential-energy surfaces?

Geometries, vibrational frequencies, and interaction energies of the CNH⋯O3 and HCCH⋯O3 complexes are calculated in a counterpoise-corrected (CP-corrected) potential-energy surface (PES) that corrects for the basis set superposition error (BSSE). Ab initio calculations are performed at the Hartree-Fock (HF) and second-order Møller-Plesset (MP2) levels, using the 6-31G(d,p) and D95++(d,p) basis sets. Interaction energies are presented including corrections for zero-point vibrational energy (ZPVE) and thermal correction to enthalpy at 298 K. The CP-corrected and conventional PES are compared; the unconnected PES obtained using the larger basis set including diffuse functions exhibits a double well shape, whereas use of the 6-31G(d,p) basis set leads to a flat single-well profile. The CP-corrected PES has always a multiple-well shape. In particular, it is shown that the CP-corrected PES using the smaller basis set is qualitatively analogous to that obtained with the larger basis sets, so the CP method becomes useful to correctly describe large systems, where the use of small basis sets may be necessary

How does basis set superposition error change the potential surfaces for hydrogen-bonded dimers?

We describe a simple method to automate the geometric optimization of molecular orbital calculations of supermolecules on potential surfaces that are corrected for basis set superposition error using the counterpoise (CP) method. This method is applied to the H-bonding complexes HF/HCN, HF/H2O, and HCCH/H2O using the 6-31G(d,p) and D95 + + (d,p) basis sets at both the Hartree-Fock and second-order Møller-Plesset levels. We report the interaction energies, geometries, and vibrational frequencies of these complexes on the CP-optimized surfaces; and compare them with similar values calculated using traditional methods, including the (more traditional) single point CP correction. Upon optimization on the CP-corrected surface, the interaction energies become more negative (before vibrational corrections) and the H-bonding stretching vibrations decrease in all cases. The extent of the effects vary from extremely small to quite large depending on the complex and the calculational method. The relative magnitudes of the vibrational corrections cannot be predicted from the H-bond stretching frequencies alone

Basis set superposition error effects, excited-state potential energy surface and photodynamics of thymine

En aquesta tesi he estudiat l'efecte de l'error de superposició de base (BSSE) en la planaritat d'algunes molècules. He observat que l'ús d'alguns mètodes de càlcul amb determinades funcions de base descriuen mínims d'energia no planars per les bases nitrogenades de l'ADN. He demostrat que aquests problemes es poden arreglar utilitzant el mètode Counterpoise per corregir el BSSE en els càlculs. En aquesta tesi també he estudiat la fotofísica de la timina i els resultats mostren que existeixen dos camins de relaxació des de l'estat excitat que permeten la regeneració de l'estructura inicial de forma ultraràpida.