¿Se debe bajar la ratio?

Se analiza la idea de que la calidad de la educación no siempre está en relación con la bajada de la ratio, sino también con el adecuado empleo de los recursos destinados a la enseñanza. Entre otros aspectos, se apuntan recursos relacionadas con el profesorado, como son, el aumento de profesionales, la mejora y ampliación de la formación, y la preparación para trabajar en distinta situaciones. Sin perder de vista que trabajar en clases pequeñas en general es beneficioso, se tienen en cuenta otros aspectos para mejorar la educación, los cuales están en relación con los objetivos que se pretendan alcanzar.

La Ratio de los jesuítas, carisma y eficacia.

En 1599 se aprobó el texto definitivo de la Ratio Studiorum, documento que daba forma al sistema educativo de los Jesuitas. Aquí se trata brevemente cómo empezó y en qué consiste este modo de educar..

La Ratio Studiorum de 1599 : un sistema educativo singular.

Resumen basado en el del autor

A comparison of discriminant logistic regression and Item Response Theory Likelihood-Ratio Tests for Differential Item Functioning (IRTLRDIF) in polytomous short tests

Resumen tomado de la publicaci??n

Afectación al ratio de solvencia mínimo requerido, producto de la aplicación del capital por riesgo operativo a los bancos parte del sistema financiero ecuatoriano, bajo el enfoque y metodología de medición planteado por Basilea II

La solvencia para la industria bancaria está medida en función del ratio que relaciona al capital regulatorio con los activos ponderados por riesgo, ésta es una medida que sirve para tener una apreciación de cuan respaldada se encuentra una institución bancaria para hacer frente a los riesgos que está expuesta por la propia inherencia del negocio. Es en este contexto que se vuelve importante el cálculo del ratio de solvencia para los bancos privados del Ecuador y el cambio o afectación que éste sufre como producto de considerar el valor por la exposición al riesgo operativo y que se considera como un requerimiento de capital. El ratio de solvencia está en función del Índice de Basilea, y, el valor de exposición al riesgo operativo está calculado por uno de los métodos que se menciona en el documento Acuerdo de Capitales o Basilea II. El presente estudio partió de comprobar que en el Ecuador es factible aplicar por parte de las entidades bancarias uno de los métodos de medición para riesgo operativo, considerando que en algunos países de Latinoamérica y en España ya lo aplican. Adicionalmente, se presenta una alternativa de aplicación en el ratio de solvencia del valor calculado para el riesgo operativo, para suavizar su resultado.

La “última ratio” del derecho constitucional ecuatoriano a la resistencia

En el año 2008, Ecuador constitucionalizó el derecho a la resistencia, el cual, desde hace varias décadas se considera un tema agotado, o por lo menos, abandonado para la teoría constitucional por considerarlo como un derecho de imposible asimilación dentro de la estructura de los contemporáneos estados de Derecho basados en la primacía de la ley y en los que la sola vigencia de las normas son su parámetro de validez, sin reparar en la justicia o injusticia del resultado obtenido producto de su aplicación. Por lo tanto, el propósito inicial del presente trabajo investigativo es brindar, desde la dogmática jurídica, una comprensión clara sobre la naturaleza del derecho a la resistencia y evidenciar su problemática y posibles alcances dentro de nuestro estado constitucional de derechos y justicia. Un segundo propósito será constatar que la validez, vigencia y eficacia del derecho a la resistencia solo será posible si su contenido se adapta al nuevo paradigma constitucional que abandera el constitucionalismo de derechos, tarea en la que no se podrá desconocer los aportes de nuestra realidad jurídica, política y social. Un propósito final, busca lograr que desde el ámbito constitucional se comprenda el postulado de la última ratio como un elemento importante y que configura el contenido esencial de este derecho que, a más de limitarlo y darle su validez, posibilita su efectiva vigencia como un recurso excepcional frente al Derecho positivo, permitiendo superar parte de la problemática que hoy le aqueja: interpretación y empleo discrecional y arbitrario, proscripción, e ineficacia.

Land/sea warming ratio in response to climate change: IPCC AR4 model results and comparison with observations

Climate model simulations consistently show that in response to greenhouse gas forcing surface temperatures over land increase more rapidly than over sea. The enhanced warming over land is not simply a transient effect, since it is also present in equilibrium conditions. We examine 20 models from the IPCC AR4 database. The global land/sea warming ratio varies in the range 1.36–1.84, independent of global mean temperature change. In the presence of increasing radiative forcing, the warming ratio for a single model is fairly constant in time, implying that the land/sea temperature difference increases with time. The warming ratio varies with latitude, with a minimum in equatorial latitudes, and maxima in the subtropics. A simple explanation for these findings is provided, and comparisons are made with observations. For the low-latitude (40°S–40°N) mean, the models suggest a warming ratio of 1.51 ± 0.13, while recent observations suggest a ratio of 1.54 ± 0.09.

On logarithmic ratio quantities and their units

The use of special units for logarithmic ratio quantities is reviewed. The neper is used with a natural logarithm (logarithm to the base e) to express the logarithm of the amplitude ratio of two pure sinusoidal signals, particularly in the context of linear systems where it is desired to represent the gain or loss in amplitude of a single-frequency signal between the input and output. The bel, and its more commonly used submultiple, the decibel, are used with a decadic logarithm (logarithm to the base 10) to measure the ratio of two power-like quantities, such as a mean square signal or a mean square sound pressure in acoustics. Thus two distinctly different quantities are involved. In this review we define the quantities first, without reference to the units, as is standard practice in any system of quantities and units. We show that two different definitions of the quantity power level, or logarithmic power ratio, are possible. We show that this leads to two different interpretations for the meaning and numerical values of the units bel and decibel. We review the question of which of these alternative definitions is actually used, or is used by implication, by workers in the field. Finally, we discuss the relative advantages of the alternative definitions.

Determination of the vibrational transition moment ratio for the Coriolis interacting v9 and v10 fundamentals of allene

Comparison between observed and calculated infrared band contours has been made to determine the vibrational transition moment ratio |M10/M9| for the Coriolis interacting ν9 and ν10 perpendicular fundamentals of allene-h4. The ratio obtained is appreciably lower than that of a previous estimate and the result obtained by integrated band intensity measurements of Overend and Crawford. From the best estimate of the ratio, the dipole moment derivatives of the two bands are determined; the value for the weaker band ν9 is subject to a large uncertainty.

Reduced height (Rht) and photoperiod insensitivity (Ppd) allele associations with establishment and early growth of wheat in contrasting production systems

Near isogenic lines (NILs) varying for genes for reduced height (Rht) and photoperiod insensitivity (Ppd-D1a) in a cv. Mercia background (rht (tall), Rht-B1b, Rht-D1b, Rht-B1c, Rht8c + Ppd-D1a, Rht-D1c, Rht12) were compared at one field site but within contrasting ('organic' vs. 'conventional') rotational and agronomic contexts, in each of 3 years. In the final year, further NILs (rht (tall), Rht-B1b, Rht-D1b, Rht-B1c, Rht-B1b + Rht-D1b, Rht-D1b + Rht-B1c) in both Maris Huntsman and Maris Widgeon backgrounds were added together with 64 lines of a doubled haploid (DH) population [Savannah (Rht-D1b) x Renesansa (Rht-8c + Ppd-D1a)]. Assessments included laboratory tests of germination and coleoptile length, and various field measurements of crop growth between emergence and pre jointing [plant population, tillering, leaf length, ground cover (GC), interception of photosynthetically active radiation (PAR), crop dry matter (DM) and nitrogen accumulation (N), far red: red reflectance ratio (FR:R), crop height, and weed dry matter]. All of the dwarfing alleles except Rht12 in the Mercia background and Rht8c in the DHs were associated with reduced coleoptile length. Most of the dwarfing alleles (depending on background) reduced seed viability. Severe dwarfing alleles (Rht-B1c, Rht-D1c and Rht12) were routinely associated with fewer plant numbers and reduced early crop growth (GC, PAR, DM, N, FR:R), and in 1 year, increased weed DM. In the Mercia background and the DHs the semi-dwarfing allele Rht-D1b was also sometimes associated with reductions in early crop growth; no such negative effects were associated with the marker for Rht8c. When significant interactions between cropping system and genotype did occur it was because differences between lines were more exaggerated in the organic system than in the conventional system. Ppd-D1a was associated positively with plant numbers surviving the winter and early crop growth (GC, FR:R, DM, N, PAR, height), and was the most significant locus in a QTL analysis. We conclude that, within these environmental and system contexts, genes moderating development are likely to be more important in influencing early resource capture than using Rht8c as an alternative semi-dwarfing gene to Rht-D1b.

Effects of prolonged conditioning on dormancy and germination of Striga hermonthica

The impact of environment on the germination biology of Striga hermonthica was studied in the laboratory by conditioning seeds at various water potentials and urea concentrations at 17.5 to 37.5°C for up to 133 days. The experimental results presented in this research are related to the effects of temperature, water potential and urea nitrogen concentration during conditioning on subsequent germination percentage of S. hermonthica. Maximum germination in S. hermonthica seeds was observed at conditioning temperatures of 20 to 25°C within the range investigated of 17.5 to 37.5°C. Water stress and also urea during conditioning suppressed maximum germination. However, the conditioning temperature ranges at which maximum germination percentages occur vary with water stress and also urea concentration. In the presence of a high concentration of urea (3.16 mM), temperatures required for maximum germination narrowed to between 17.5 to 20°C. The optimum period of conditioning decreased with increase in water stress and also urea concentration similar to previous reports. The implications of these findings on Striga hermonthica field infestations have been investigated and being reported in another paper. Germination was greatly suppressed by conditioning environments including 3.16 mM urea and at 37.5°C. At the high concentration of 3.16 mM, temperatures required for maximum germination narrowed to between 17.5 and 20°C. Optimum conditioning period decreased with water stress and with increase in urea concentration.

Modelling effects of prolonged conditioning on dormancy and germination of Striga hermonthica

The impact of environment on the germination biology of the parasite was studied in the laboratory with seeds conditioned at various water potentials, urea concentrations and at 17.5 to 37.5°C for up to 133 days. Maximum germination was observed at 20 to 25°C. Water stress and urea suppressed maximum germination. The final percentage germination response to period of conditioning showed a non-linear relationship and suggests the release of seeds from dormancy during the initial period and later on dormancy induction. Germination percentage increased with increase in conditioning period to a threshold and remained stable for variable periods followed by a decline with further extension of conditioning time. The decline in germination finally terminated in zero germination in most treatments before the end of experimentation. The investigated factors of temperature, water potential and urea showed clear effects on the expression of dormancy pattern of the parasite. The effects of water potential and urea were viewed as modifying a primary response of seeds to temperature during conditioning. The changes in germinability potential during conditioning were consistent with the hypothesis that dormancy periods are normally distributed within seed populations and that loss of primary dormancy precedes induction of secondary dormancy. Hence an additive mathematical model of loss of primary dormancy and induction of secondary as affected by environment was developed as: G = {[Φ-1 (Kp+ (po+pnN+pwW) (T-Tb) t)]-[Φ-1 (Ks+ ((swW+sa)+sorT)t)]}[Φ-1(aT2+bT+c+cwW)].

Seed dormancy and germination of Ficus lundellii and tropical forest restoration

We investigated seed dormancy and germination in Ficus lundellii Standl. (Moraceae), a native species of Mexico's Los Tuxtlas tropical rain forest. In an 8-h photoperiod at an alternating diurnal (16/8 h) temperature of 20/30 degrees C, germination was essentially complete (96%) within 28 days, whereas in darkness, all seeds remained dormant. Neither potassium nitrate (0.05-0.2%) applied continuously nor gibberellic acid applied either continuously (10-200 ppm) or as a 24 hour pretreatment (2000 ppm) induced germination in the dark. Germination in the light was not reduced by a 24-h hydrochloric acid (0.1-1%) pretreatment, but it was reduced both by a 24-h pretreatment with either H2O2 (0. 1-5 M) or 5% HCl, or by more than 5 days of storage at 40 degrees C (4.5% seed water content). In a study with a 2-dimensional temperature gradient plate, seeds germinated fully and rapidly in the light at a constant temperature of 30 degrees C, and fully but less rapidly in the light at alternating temperatures with low amplitudes (< 12 degrees C) about the optimal constant temperature. The base, optimal and ceiling temperatures for rate of germination were estimated as 13.8, 30.1 and 41.1 degrees C, respectively. In all temperature regimes, light was essential for the germination of F lundellii seeds.