978 resultados para growth parameters
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A utilização de funções matemáticas para descrever o crescimento animal é antiga. Elas permitem resumir informações em alguns pontos estratégicos do desenvolvimento ponderal e descrever a evolução do peso em função da idade do animal. Também é possível comparar taxas de crescimento de diferentes indivíduos em estados fisiológicos equivalentes. Os modelos de curvas de crescimento mais utilizados na avicultura são os derivados da função Richards, pois apresentam parâmetros que possibilitam interpretação biológica e portanto podem fornecer subsídios para seleção de uma determinada forma da curva de crescimento em aves. Também pode-se utilizar polinômios segmentados para descrever as mudanças de tendência da curva de crescimento animal. Entretanto, existem importantes fatores de variação para os parâmetros das curvas, como a espécie, o sistema de criação, o sexo e suas interações. A adequação dos modelos pode ser verificada pelos valores do coeficiente de determinação (R2), do quadrado médio do resíduo (QM res), do erro de predição médio (EPm), da facilidade de convergência dos dados e pela possibilidade de interpretação biológica dos parâmetros. Estudos envolvendo modelagem e descrição da curva de crescimento e seus componentes são amplamente discutidos na literatura. Porém, programas de seleção que visem a progressos genéticos para a forma da curva não são mencionados. A importância da avaliação dos parâmetros dos modelos de curvas de crescimento é ainda mais relevante já que os maiores ganhos genéticos para peso estão relacionados com seleção para pesos em idades próximas ao ponto de inflexão. A seleção para precocidade pode ser auxiliada com base nos parâmetros do modelo associados à variáveis que descrevem esta característica genética dos animais. Esses parâmetros estão relacionados a importantes características produtivas e reprodutivas e apresentam magnitudes diferentes, de acordo com a espécie, o sexo e o modelo utilizados na avaliação. Outra metodologia utilizada são os modelos de regressão aleatória, permitindo mudanças graduais nas covariâncias entre idades ao longo do tempo e predizendo variâncias e covariâncias em pontos contidos ao longo da trajetória estudada. A utilização de modelos de regressões aleatórias traz como vantagem a separação da variação da curva de crescimento fenotípica em seus diferentes efeitos genético aditivo e de ambiente permanente individual, mediante a determinação dos coeficientes de regressão aleatórios para esses diferentes efeitos. Além disto, não há necessidade de utilizar fatores de ajuste para a idade. Esta revisão teve por objetivos levantar os principais modelos matemáticos frequentistas utilizados no estudo de curvas de crescimento de aves, com maior ênfase nos empregados com a finalidade de estimar parâmetros genéticos e fenotípicos.
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
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Pareiorhina rudolphi was sampled in streams of the Ribeirao Grande system, eastern Serra da Mantiqueira (22[degree]47[minute]08[second]S, 45[degree]28[minute]17[second] W). Samplings were carried out using an electrofishing device, during the months of July/2001, October/2001, February/2002 and April/2002. Sex-ratio diverged significantly from the expected 1: 1 ratio([chi]2 = 6.53; p < 0.05), standing at 1.6:1 (female: male). The spawning period for Pareiorhina rudolphi lasts from spring to summer, with, the highest observed, in October and February by the gonadosomantic index and the relative condition factor coincided with the spawning period. The length at sexual maturity of P. rudolphi is about 4.45 cm for both sexes. The absolute fecundity was low, and ranged from 4 to 11 oocytes. The periphyton was used as a direct food source by the species, which remain attached to the substrate with their large circular lips, and use their conspicuous Slightly Yellowish teeth to graze the periphyton. The growth parameters, natural mortality rate and survival rate for P, rudolphi were respectively: K = 0.35 year-1, L[infinity] = 7.2 cm, tmax = 8.6 years, M = 1.1 year-1, S = 33%. The characteristics presented by P. rudolphi occur in the environment function of a population adjustment, and not of species abundance.
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We investigate the formation of compositional modulation and atomic ordering in InGaP films. Such bulk properties - as well as surface morphologies - present a strong dependence on growth parameters, mainly the V/III ratio. Our results indicate the importance of surface diffusion and, particularly, surface reconstruction for these processes. Most importantly from the application point of view, we show that the compositional modulation is not necessarily coupled to the surface instabilities, so that smooth InGaP films with periodic compositional variation could be obtained. This opens a new route for the generation of templates for quantum dot positioning and three-dimensional arrays of nanostructures. © 2007 American Institute of Physics.
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In low-order streams, the high and variable water flow rates offer both advantages and disadvantages to the life cycle of fishes. Even closely related species living in similar habitats can show differences in life history patterns. Based on oocyte-size distributions, C. lauroi was classified into the fractional spawning type, and C. alipioi into the total spawning type. The absolute fecundity of C. lauroi ranged from 1,313 to 2,925 oocytes; in C. alipioi the absolute fecundity ranged from 2,213 to 25,550 oocytes. The nonparametric Spearman correlation test showed statistical significance between the gonadosomatic index and fecundity for both species. The growth parameters, natural mortality rate and survival rate for females of C. lauroi were: K = 0.68 yr -1, L ∞ = 8.7 cm, t max = 4.4 years, M= 1.62 yr -1, S = 19.79%, and for males: K = 0.78 yr -1, L ∞ = 6.9 cm, t max = 3.8 years, M = 1.89 yr -1, S = 15.11%. The growth parameters, natural mortality rate and survival rate for females of C. alipioi were: K = 0.90 yr -1, L ∞ = 12.2 cm, t max = 3.3 years, M = 1.81 yr -1, S = 16.37%, and for males: K = 0.76 yr -1, L ∞ = 10.1 cm, t max = 3.9 years, M = 1.71 yr -1, S = 18.10%.
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Nile tilapia (Oreochromis niloticus), which is exotic to South America, is the most common species caught in artisanal fisheries at the Barra Bonita Reservoir, Southeastern Brazil. This species is of great socioeconomic importance for the region and keeps active a population of about 500 fishers. In the present study we assess reproduction, food dynamics and level of exploitation of O. niloticus, caught by artisanal fisheries in the Barra Bonita Reservoir. Specimens were collected monthly, from July 2004-June 2005, and a total of 1 715 specimens were analyzed. Each specimen was examined to obtain biological and biometric data: standard length (cm), total weight (g), reproductive data (sex and stage of maturation), and stomach contents (empty, partly full, and full). We also estimated the sex ratio (by macroscopic observation of gonads), reproductive period (by ovarian development and seasonal average of gonadosomatic index in females), and feeding habits (by stomach contents). The possible relationship between abiotic factors and the reproductive period was statistically verified using Spearman's Rank Correlation. The FiSAT (ELEFAN I) package was used to assess growth parameters, mortality rates and to infer exploitation rate from standard length frequencies. The O. niloticus population had a sex ratio of 1.3:1 (M:F). Results indicated that ripe females were captured throughout the year, with a higher frequency during the winter-2004 (with a frequency of 59%, at a mean temperature of 20.5°C), and in spring-2004 (with a frequency of 60.5% at a mean temperature of 21.18°C). The GSI mean values obtained by season were: winter-2004: 1.71; spring-2004: 1.72; summer-2005: 0.80, and autumn-2005: 1.19. The Spearman correlation indicated positive values with respect to pH, dissolved oxygen, electric conductivity, transparency and chlorophyll a, and negative values with respect to temperature, accumulated rainfall and altimetric benchmark. The main food items were phytoplankton and periphytic algae, observed in 99.6% of the analyzed stomachs. The estimated growth and mortality parameters were: L∞=33.60cm, k=0.63/year, longevity= 4.76years, Z=2.81/ year, M=1.20/year and F=1.61/year. The weight-length relationship was Ln Wt=-2.8532+2.8835 Ln Lp. The estimated yield per recruit values were as follows: E=0.570, Emax=0.776, E0.1=0.604 and E0.5=0.349. These results indicate that a well established population of O. niloticus is present at Barra Bonita Reservoir; with an active reproduction throughout the year, more intense during winter and spring, and that O. niloticus is a phytoplanktophagus species. There were no indications that this species is being overfished, we therefore recommend that, due to its exotic condition, no restrictions need to be taken on its fishing activities.
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Although there are recommendations for the fertilization of commercial squash crops, studies which connect the effect of topdressing potassium fertilization and yield are still rare. Thus, this study aimed at evaluating topdressing potassium doses on squash (Mirian hybrid) yield, in an experimental farm of the Universidade Estadual Paulista Júlio de Mesquita Filho, in São Manuel, São Paulo State, Brazil. The experimental design was randomized blocks, with five treatments (0.0 kg ha-1, 50.0 kg ha-1, 100.0 kg ha-1, 200.0 kg ha-1 and 400.0 kg ha-1 of K2O) and six replications. Plant growth parameters, yield and fruit quality were evaluated. After harvesting, plant (leaves + stem) and soil macronutrients were submitted to chemical analysis and data to variance and regression analysis. It was concluded that the highest yield resulted from the topdressing dose of 199.0 kg ha-1 of K2O. A reduction in calcium and magnesium contents in the plant canopy and a higher K+ content in the soil were observed for increasing K2O levels.
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This study aimed to define the best substrate and temperature for the emergence of Phacelia sp. seedling, annual ornamental flower gardens. The experimental design was entirely randomized in a factorial scheme 37 (three different types of substrates: vermiculite, sand and sphagnum combined with seven temperature conditions: room temperature, constant at 20, 25, 30 and 35C, and alternated at 20-30C and 25-35C) with 4 replications of 100 seeds each. Emergence (%E) and Emergence Rate (ER) were evaluated. The means of the resulting values were then compared by the Tukey test at 5% confidence level. There was a significant interaction amongst substrates and temperatures for all analyzed variables. For seeds sown in vermiculite and sand, the seedlings had higher %E and emerged fastest at 20C, room temperature and 20-30C that did not present statistically significant data. In sphagnum, seedlings showed greater %E in the alternated at 20-30C, room temperature and 20C and emerged quickly at room temperature and 20C that did not present statistically significant data. At room temperature and 20C, the seedlings had higher %E and emerged faster in vermiculite and sand that did not present statistically significant data. At 25, 30 and 25-35C, the seedlings showed better %E and emerged fastest in sand. At 35C, the seedlings showed either in vermiculite and sand were not significantly different in their emergence, but emerged faster in sand. There was not significantly different among substrates in their emergence at 20-30C, but the seedlings emerged faster in vermiculite and sand. It was concluded that the Phacelia sp. seedlings in all substrates showed greater %E at room temperature, 20C and 20-30C. For all temperatures, the seedlings growth parameters were superior when seeds were sown in sand.
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
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Pós-graduação em Agronomia (Irrigação e Drenagem) - FCA
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Pós-graduação em Ciência Animal - FMVA
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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)