947 resultados para MONO-N-DEALKYLDISOPYRAMIDE
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2001
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Traditionally, language speakers are categorised as mono-lingual, bilingual, or multilingual. It is traditionally assumed in English language education that the ‘lingual’ is something that can be ‘fixed’ in form, written down to be learnt, and taught. Accordingly, the ‘mono’-lingual will have a ‘fixed’ linguistic form. Such a ‘form’ differs according to a number of criteria or influences including region or ‘type’ of English (for example, World Englishes) but is nevertheless assumed to be a ‘form’. ‘Mono-lingualism’ is defined and believed, traditionally, to be ‘speaking one language’; wherever that language is; or whatever that language may be. In this chapter, grounded in an individual subjective philosophy of language, we question this traditional definition. Viewing language from the philosophical perspectives such as those of Bakhtin and Voloshinov, we argue that the prominence of ‘context’ and ‘consciousness’ in language means that to ‘fix’ the form of a language goes against the very spirit of how it is formed and used. We thus challenge the categorisation of ‘mono’-lingualism; proposing that such a categorisation is actually a category error, or a case ‘in which a property is ascribed to a thing that could not possibly have that property’ (Restivo, 2013, p. 175), in this case the property of ‘mono’. Using this proposition as a starting point, we suggest that more time be devoted to language in its context and as per its genuine use as a vehicle for consciousness. We theorise this can be done through a ‘literacy’ based approach which fronts the context of language use rather than the language itself. We outline how we envision this working for teachers, students and materials developers of English Language Education materials in a global setting. To do this we consider Scotland’s Curriculum for Excellence as an exemplar to promote conscious language use in context.
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Doctorat en Sciences
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El paisaje de la pampa arenosa fue construido sobre antiguas geoformas medanosas que determinaron la presencia de suelos muy disímiles coexistiendo a nivel de lote. En los últimos años, fue aumentando la superficie destinada al cultivo de granos a expensas de las pasturas. Los objetivos generales fueron evaluar el secuestro de carbono y la calidad de suelos mono y poligenéticos bajo distintos usos, considerando las propiedades más sensibles a modo de lograr un conjunto mínimo para un monitoreo más simple de los cambios en la calidad de los suelos de la región. Se muestrearon dos situaciones de uso; agricultura continua (AGRICOLA) y en rotación con pasturas (MIXTO), evaluadas en dos subgrupos taxonómicos; Hapludoles énticos (HE) y Hapludoles thapto árgicos (HTA), considerándose dos profundidades 0-10 cm y 10-20 cm. De cada situación (USO SUELO) se realizaron tres repeticiones. Las propiedades determinadas fueron: carbono orgánico total (COT), carbono orgánico particulado (COP), carbono orgánico asociado a la fracción mineral (COM), densidad aparente (DAP), resistencia a la penetración (RP), infiltración básica (IB), índice de estructura (IE) y estabilidad de agregados (PromE), distinguiendo mediante diferentes pretratamientos (Le Bissonnais, 1996) entre mecanismos de desagregación (HRap, HLen, Heta). Los mejores indicadores de calidad dinámica para conformar un conjunto mínimo de aplicación en la región fueron HRap, COP y DAP. Estos indicadores mostraron que los suelos en rotación presentaron una condición de calidad superior. Las propiedades de mayor divergencia entre tipos de suelos fueron las relacionadas con sus diferencias texturales: COM, DAP, RP, IE y Heta. El método de Le Bissonnais presentó gran habilidad para detectar los mecanismos de desagregación que más condicionan la estabilidad de los suelos bajo las situaciones de uso evaluadas. Si bien se percibieron cambios en la distribución vertical del COT entre usos y suelos, la capacidad de secuestro de carbono hasta el metro de profundidad fue similar.
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A cytochrome P-450-dependent benzo[a]pyrene mono-oxygenase enzyme system (BPM) has been identified and partially characterized in males of the shore crab Carcinus maenas (L.). Apparent Km values obtained at 30 °C using microsomal preparations from the antennary glands of animals collected during summer were in the range 1.61–2.11 µM. The cytochrome P-450 content was 0·022 nmol/mg microsomal protein when BPM activity in the same preparation was 0·085 nmol/mg protein/min.
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Isentropic compressibilities ?S, and excess isentropic compressibilities ?SE have been determined from measurements of speeds of sound u and densities ? of 14 binary mixtures of triethylamine (TEA) and tri-n-butylamine (TBA) with n-hexane, n-octane, iso-octane, n-propylamine, n-butylamine, n-hexylamine and n-octylamine. The relative magnitude and sign of ?SE have been interpreted in terms of molecular interactions and interstitial accommodation. The values of ?SE for TEA + alkane are positive while for TBA + alkane are negative. The values of ?SE for TEA + primary amine become progressively less positive and eventually to negative with the increase in chain length of alkylamine. In case of TBA + primary amine, the values of ?SE increase from n-propylamine to n-butylamine, and then decrease with chain length of primary amine. The experimental speeds of sound u have been analyzed in terms of collision factor theory, free length theory and Prigogine–Flory–Patterson statistical theory of solutions.
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Toluene dioxygenase (TDO)-catalysed monooxygenation of methylsulfanylmethyl phenyl sulfide 1 and methylsulfanylmethyl 2-pyridyl sulfide 4, using whole cells of Pseudomonas putida UV4, occurred exclusively at the alkyl aryl sulfur centre to yield the alkyl aryl sulfoxides 2 and 5 respectively. These sulfoxides, accompanied by the dialkyl sulfoxides 3 and 6, were also obtained from naphthalene dioxygenase (NDO)-catalysed sulfoxidation of thioacetals 1 and 4 using intact cells of P. putida NCIMB 8859. Enzymatic oxidation of methyl benzyl sulfide 7, 2-phenyl-1,3-dithiane 19, and 2-phenyl-1,3-dithiolane 23, using TDO, gave the corresponding dialkyl sulfoxides 8, 20 and 24 as minor bioproducts. TDO-catalysed dioxygenation of the alkyl benzyl sulfides 7, 15 and 17 and the thioacetals 19 and 23, with P. putida UV4, yielded the corresponding enantiopure cis-dihydrodiols 9, 16, 18, 21 and 25 as major metabolites and cis-dihydrodiol sulfoxides 14, 22 and 26 as minor metabolites, resulting from a tandem trioxygenation of substrates 7, 19 and 23 respectively. Chemical oxidation, of the enantiopure cis-dihydrodiol sulfides 9, 16, 18 and 21 with dimethyldioxirane (DMD), gave separable mixtures of the corresponding pairs of cis-dihydrodiol sulfoxide diastereoisomers 14 and 27, 28 and 29, 30 and 31, 22 and 32. While dialkyl sulfoxide bioproducts 3, 6, 20 and 24 were of variable enantiopurity (27-greater than or equal to 98% ee), alkyl aryl monosulfoxides 2 and 5, cis-dihydrodiols 9, 16, 18, 21 and 25 and cis-dihydrodiol sulfoxide bioproducts 14, 22 and 26 were all single enantiomers (greater than or equal to 98% ee). The absolute configurations of the products, obtained from enzyme-catalysed (TDO and NDO) and chemical (DMD) oxidation methods, were determined by stereochemical correlation, circular dichroism, and X-ray crystallographic methods.