990 resultados para Equação de Ångström


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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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The pH values near a planar dissociating membrane are studied under a mean field approximation using the Poisson-Boltzmann equation and its linear form. The equations are solved in planar symmetry with the consideration that the charge density on the dissociating membrane surface results from an equilibrium process with the neighboring electrolyte. Results for the membrane dissociation degree are presented as a function of the electrolyte ionic strength and membrane surface charge density. Our calculations indicate that pH values have an appreciable variation within 2 nm from the membrane. It is shown that the dissociation process is enhanced due to the presence of bivalent ions and that pH values acquire better stability than in an electrolyte containing univalent ions.

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The one-dimensional Schrödinger equation with the singular harmonic oscillator is investigated. The Hermiticity of the operators related to observable physical quantities is used as a criterion to show that the attractive or repulsive singular oscillator exhibits an infinite number of acceptable solutions provided the parameter responsible for the singularity is greater than a certain critical value, in disagreement with the literature. The problem for the whole line exhibits a two-fold degeneracy in the case of the singular oscillator, and the intrusion of additional solutions in the case of a nonsingular oscillator. Additionally, it is shown that the solution of the singular oscillator can not be obtained from the nonsingular oscillator via perturbation theory.

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Investiga-se a equação de Schrödinger unidimensional com uma classe de potenciais V(|x|) que se anulam no infinito e apresentam singularidade dominante na origem na forma α/|x|β(0 < β < 2). A hermiticidade dos operadores associados com quantidades físicas observáveis é usada para determinar as condições de contorno apropriadas. Dupla degenerescência e exclusão de soluções simétricas, consoante o valor de β, são discutidas. Soluções explícitas para o átomo de hidrogênio e o potencial de Kratzer são apresentadas.

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PURPOSE: To measure fetal renal volume in normoglycemic and hyperglycemic pregnancies. METHODS: A longitudinal prospective study was conducted and included 92 hyperglycemic and 339 normoglycemic pregnant women attended at the prenatal service of a hospital from Rio de Janeiro State. Ultrasound examinations were performed to estimate gestational age at baseline and the kidney volume was estimated using the prolate ellipsoid volume equation. RESULTS: Fetal kidney volume growth between normoglycemic and hyperglycemic pregnancies are significantly different. The fetal kidney volume growth in pregnancy is positively correlated with gestational age explained by these predictor equations, by group: normal renal volume = exp (6.186+0.09×gestational week); hyperglycemic renal volume = exp (6.978+0.071×gestational week) and an excessive growth pattern for hyperglycemic pregnancies may be established according to gestational age. CONCLUSION: This is important for early detection of abnormalities in pregnancy, particularly in diabetic mothers.

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The Schwinger quantum action principle is a dynamic characterization of the transformation functions and is based on the algebraic structure derived from the kinematic analysis of the measurement processes at the quantum level. As such, this variational principle, allows to derive the canonical commutation relations in a consistent way. Moreover, the dynamic pictures of Schrödinger, Heisenberg and a quantum Hamilton-Jacobi equation can be derived from it. We will implement this formalism by solving simple systems such as the free particle, the quantum harmonic oscillator and the quantum forced harmonic oscillator.

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Leaf area estimate may contribute to understand the relationships of interference among weeds and crops. The objective of this research was to obtain a mathematical equation to estimate the leaf area of Euphorbia heterophylla based on linear measures of the leaf blade. Correlation studies were carried out using the real leaf area and leaf length (C) and the maximum leaf width (L) of 200 leaf blades which were collected from several agroecosystems at Universidade Estadual Paulista in Jaboticabal, SP, Brazil. The evaluated statistic models were: linear Y = a + bx; simple linear Y = bx; geometric Y = ax b; and exponential Y = ab x. All of the evaluated models can be used for E. heterophylla leaf area estimation. The simple linear regression model is suggested using C*L and taking the linear coefficient equal to zero. Thus, an estimate of the leaf area of E. heterophylla can be obtained using the equation Af' = 0.6816*(C*L).

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The objective of this work was to determine nutrient deposition on the carcass of bullfrog (Lithobates catesbeianus) tadpoles using a nonlinear model. A total of 2,700 tadpoles with an average weight of 0.039 g were used. Commercial ground feed containing 55% crude protein was offered ad libitum. The animals were weighed and evaluated every ten days for analysis of crude protein, ether extract, water, and mineral salt contents. The parameters of the Gompertz model were estimated by the modified Gauss-Newton method, and the deposition rates (g per day) over time were calculated by the resulting equation. The values found for the parameters of the Gompertz equation, used to describe nutrient deposition on tadpole carcass, showed biological interpretation. Maximum deposition rate (t*) was observed on the 36.2331th day for protein, on the 37.1420th day for water, on the 35.2971th day for mineral salt, and on the 41.3547th day for fat. Nutrient intake from the diet is higher than the deposition rate on the tadpole carcass.

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The aim of the present study was to determine the size at sexual maturity in the freshwater crab Dilocarcinus pagei Stimpson, 1861, from a population located in Mendonça, state of São Paulo, Brazil. The crabs were sampled monthly (July 2005 to June 2007), at Barra Mansa reservoir. The specimens were captured manually or in sieves passed through the aquatic vegetation. The crabs were captured and separated by sex based on morphology of the pleon and on the number of pleopods. The following dimensions were measured: carapace width (CW); carapace length (CL); propodus length (PL); and abdomen width (AW). The morphological analysis of the gonads was used to identify and categorize individuals according to their stage of development. The morphological maturity was estimated based on the analysis of relative growth based on the allometric equation y = ax b. The gonadal maturity was based on the morphology of the gonads by the method CW50 which indicates the size at which 50% of the individuals in the population showed gonads morphologically mature to reproduction. The biometric relationships that best demonstrated the different patterns of growth for the juvenile and adult stages were CW vs. PL for males and CW vs. AW for females (p<0.001). Based on these relationships, the estimated value to morphological sexual maturity was 21.5 mm (CW) in males and 19.7 mm (CW) in females. The determination of the size at sexual maturity and the adjustment of the data based on the logistic curve (CW50) resulted in a size of 38.2 mm for males and 39.4 mm for females (CW). Based on the data obtained for sexual maturity for D. pagei, we can estimate a minimum size for capture of 40 mm (CW). This minimum size allows at least half of the population to reproduce and retains the juveniles and a portion of the adults in the population.

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The objective of this study was to obtain a mathematical equation to estimate the leaf area of Panicum maximum using linear measures of leaf blade. Correlation studies were conducted involving the real leaf area (Sf), the main vein leaf length (C), and the maximum leaf width (L). The linear and geometric equations related to C provided good leaf area estimates. For practical reasons, the use of an equation involving only the C*L product is suggested. Thus, an estimate of P. maximum leaf area can be obtained by the equation Sf = 0.6058 (C*L), with the coefficient of determination R = 0.8586.

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Pós-graduação em Agronomia (Irrigação e Drenagem) - FCA