693 resultados para Mimosa scabrella (Benth.)


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Algumas espécies de leguminosas arbóreas, associadas a bactérias fixadoras de nitrogênio e a fungos micorrízicos, têm apresentado bom desenvolvimento em solos degradados. Visando avaliar a influência dessas espécies na recuperação da fertilidade do solo, mediu-se a quantidade de matéria seca e nutrientes no material formador da serapilheira, durante o ano de 1995, e na serapilheira acumulada na superfície do solo, em 1995 e 1996, e estimou-se sua velocidade de decomposição. Estudaram-se povoamentos homogêneos de Mimosa caesalpiniifolia (sabiá), Acacia mangium e Acacia holosericea, em espaçamento de 4 m²/planta, em Planossolo, no campo experimental da Embrapa Agrobiologia, município de Seropédica (RJ) (22°49' S e 43°38' W, com altitude variando entre 18 e 33 m). A deposição média anual de material formador da serapilheira foi de 10 Mg ha-1, para o sabiá, e de 9 Mg ha-1, para as Acacias Em média, as folhas corresponderam a 64% do material formador da serapilheira produzido pelo sabiá e pela Acacia holosericea e 70% para Acacia mangium A parte mais rica em nutrientes do material formador da serapilheira foram as estruturas reprodutivas. A Acacia Mangium foi a espécie de maior capacidade de retranslocação interna de nutrientes, produzindo a serapilheira mais pobre em nutrientes e de menor velocidade de decomposição. A serapilheira produzida pelo sabiá foi a mais rica em nutrientes, com menor tempo de residência. As diferentes velocidades de decomposição da serapilheira dessas espécies podem ser utilizadas como estratégia para complementar necessidades nutricionais de culturas econômicas em sistemas agroflorestais e, ou, para auxiliar na recuperação de solos degradados.

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Realizou-se um experimento em casa de vegetação com o objetivo de avaliar os efeitos da inoculação com fungos micorrízicos arbusculares (FMAs) e, ou, rizóbio, associados à adição de resíduo da fabricação de ácido láctico (Ferkal), na produção de mudas de Mimosa caesalpiniaefolia (sabiá) em estéril de extração de argila. Foram utilizados vasos plásticos de 6 L que continham estéril de extração de argila, adicionado do resíduo Ferkal (nas concentrações de 0, 50, 100 e 200 g dm-3). Foram empregados seis tratamentos microbiológicos (FMAs nativos; FMA Glomus clarum; rizóbio; FMAs nativos + rizóbio; FMA G. clarum + rizóbio, e controle não inoculado). Após 103 dias, as mudas foram coletadas, e analisados o peso da matéria seca dos nódulos, a taxa de colonização micorrízica, o peso da matéria seca e os teores de N e P na parte aérea das mudas. Os resultados demonstraram que adição de Ferkal no tratamento-controle (sem inoculação) aumentou significativamente o teor de P. Entretanto, as melhores respostas foram obtidas nas mudas inoculadas com FMAs e, ou, rizóbio, que apresentaram, em relação ao controle, aumentos significativos no peso da matéria seca e nos teores de N e P da parte aérea das mudas, em quase todos os tratamentos inoculados. Os FMAs nativos foram mais eficientes que o FMA G. clarum em promover o crescimento de M. caesalpiniaefolia.

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Extrafloral nectaries (EFNs) are structurally variable and widely spread among the angiosperms. The occurrence of EFNs in leaves of Pterodon polygalaeflorus Benth. and Pterodon pubescens Benth. (Fabaceae: Papilionoideae) were detected in adult specimens, at the time of production of new buds and flowers. The goals of the present study are to register the occurrence of the EFNs in P. pubescens and P. polygalaeflorus, and provide comparative data on the anatomical structures. The EFNs occur in the rachis and are located under the insertion of each petiolule. Each nectary consists of a small elevation whose apical portion is deeply invaginated, resulting in a depression (secretory pole), a common characteristic of both species. Unicellular, nonglandular trichomes occur along the rachis, being less numerous in P. polygalaeflorus while in P. pubescens they cover the EFNs. The secretory tissue consists of parenchyma cells with dense cytoplasm compactly arranged. The nectar reaches the surface of the EFNs by rupturing the thin cuticle which covers the secretory pole, since both species lack stomata or any other interruption at the epidermis. The basic difference between the two species, in relation to the EFNs, is the density of the pubescence, which is always greater in P. pubescens. Structural and dimensional modifications may be observed, even between basal and apical nectaries in the same rachis, so it does not constitute a taxonomical tool.

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Conduziu-se um experimento com o objetivo de estudar a eficácia agronômica e econômica de herbicidas para o controle de duas sérias plantas daninhas de pastagens: Acacia farnesiana e Mimosa pteridofita. Os produtos utilizados, por meio de pincelamento no toco, foram o óleo diesel, óleo lubrificante usado de trator, solução aquosa de 2,4-D + picloram e solução oleosa de 2,4-D + picloram. À exceção do óleo lubrificante, os herbicidas foram testados em dois tamanhos de planta daninha e duas alturas de corte. Avaliaram-se a porcentagem de controle e o vigor de brotação das plantas não-controladas. Concluiu-se que o corte das plantas só é eficiente no controle das duas espécies, quando realizado no nível do solo e seguido da aplicação de herbicida específico, como o 2,4-D + picloram. O óleo diesel também controla totalmente ambas as espécies, e com menores custos que o 2,4-D + picloram, porém apenas quando aplicado nas plantas mais jovens. Há incompatibilidade entre o óleo diesel e o 2,4-D + picloram no controle das duas espécies. O óleo lubrificante usado não apresenta nenhum efeito herbicida em plantas adultas destas espécies.

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This paper describes the chemical constituents isolated from leaves and fruits of Licania tomentosa Benth. The plant materials were successively extracted with hexane and methanol. From the extracts the following compounds were obtained: betulinic acid; licanolide, a new triterpene lactone; oleanolic acid, lupeol; palmitoleic and hexadecanoic acid; a mixture of stigmasterol and sitosterol; and a mixture of tormentic, ursolic and betulinic acid. The structures of the natural products were identified on the basis of spectral data.

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Foliar analysis of biochemical parameters were carried out in order to investigate the influence of air pollutants on two tropical tree species (Licania tomentosa (Benth.) and Bauhinia forfícata (Link.)). Special attention was given to tropospheric ozone due to the fact that concentration levels in the region were found to be up to 140 µg m-3 for a 4 h average time, which is well above the value that can cause injuries to orchides and tobacco (59 µg m-3). Other pollutants such as nitrogen and sulphur oxides were measured and their ambient concentrations were also associated to biochemical alterations in the investigated species.

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The aim of this work was to evaluate the influence of five storage times of dry leaves of two patchouli genotypes on its essential oil content and chemical composition. Harvest was realized four months after planting. Storage influenced essential oil content of genotype POG-002. Patchoulol was the majority compound. Storage of dry leaves increased significatively the content of the compounds α-bulnesene and germacrene A of genotype POG-021 and longicanfenilone, pogostol and patchoulol of POG-002. However, storage reduced significatively the content of the compounds cicloseichelene, β-cariofilene, α-guaiene, acifilene and α-bulnesene of the essential oil of genotype POG-002.

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Chemical investigation of Hyptidendron canum stems resulted in the isolation of betulinic, ursolic and euscaphic acids. From the leaves were isolated 3β-O-β-galactopiranosilsitosterol, ursolic aldehyde, and mixtures of maslinic acid and 2α-hydroxyursolic acid, α and β-amyrin, uvaol and erythrodiol, sitosterol and stigmasterol, spathulenol and globulol. Hexane and chloroform leave fractions as well as ursolic and betulinic acids showed antifungal activities against the yeast form of Paracoccidioides brasiliensis.

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This work describes the phytochemical study of stems of Mimosa invisa (Mimosaceae) and the evaluation of the antioxidant potential of isolated compounds. Cromatografic techniques were employed to isolate salicifoliol, pinoresinol, quercetin, quercetin-3-O-rhamnopyranosyl, quercetin-3-O-arabinofuranosyl lupeol, β-amyrin, sitosterol, p-hydroxy coumaric acid, 4-hydroxy-3-methoxy benzaldehyde (vanillin), 4-hydroxy-3,5-dimethoxy benzaldehyde, 4-hydroxy-3-methoxy benzoic acid and 4',6,7- trimethoxy flavonol. The latter had been previously described but the spectrometric data shown indicated the structure required review. The antioxidant activity of the compounds was evaluated by the DPPH test and capability of NBT reduction by superoxide radicals. Quercetin glycosides showed lower antioxidant potential than quercetin and, salicifoliol was found to be more active than pinoresinol.

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Caesalpinia peltophoroides is a domesticated tree found in Brazil. It was necessary to develop an analytical method to determine the content of total polyphenols (TP) in this herbal drug. The pre-analytical method was standardized for analysis time, wavelength, and the best standard to use. The optimum conditions were: pyrogallol, 760 nm, and 30 min respectively. Under these conditions, validation by UV/Vis spectrophotometry proved to be reliable for TP of the crude extract and semipurified fractions from C. peltophoroides. Standardization is required for every herbal drug, and this method proved to be linear, precise, accurate, reproducible, robust, and easy to perform.

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The phytochemical investigation of L. macrophylla Benth led to the isolation of a new flavanol named licanol: (-)-4'-O-methyl-epigallocatechin-3'-O-α-L-rhamnoside, along with nine known compounds, identified as: (-)-4'-O-methyl-epigallocatechin, pheophytin A, 13²-hydroxy-(13²-S)-pheophytin A, pheophytin B, sitosterol, stigmasterol, sitosterol-β-O-glucoside, betulinic alcohol and oleanolic acid. The structures were established based on IR, HR-ESI-MS, and NMR spectrometric data analysis with the aid of 2D techniques. The methanolic extracts of leaves and stem bark as well as the compounds licanol, 13²-hidroxi-(13²-S)-feofitina A, and betulinic alcohol demonstrated antimicrobial activity against several bacterial strains.

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This the first phytochemical investigation of Mimosa artemisiana (Leguminosae-Mimosoideae) describing the isolation and identification of quercitrin, myricitrin, 3,5,4´-trihydroxi-6,7-dimethoxyflavone (6,7-dimethylkaepferol), flavolignans, 3-O-β-D-glucopyranosil sitosterol, lupeol, sitostenone, stigmastenone, campestenone, sitosterol, stigmasterol, campesterol, methyl indole-3-carboxilate and indole-3-carboxaldehyde in the extracts from the leaves and wood of this plant. This is the first registry of 6,7-dimethoxy,4'-hydroxy-flavona and the flavonolignans in this genera. The isolation of all metabolites was made by chromatographic methods and the structures were established on the basis of IR, MS, ¹H and 13C NMR spectra analysis, comparison with literature data and GC-MS of mixtures analysis.

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Cyclolignan (+)-lyoniresinol (1), veratric acid (2), vanillic acid (3), lupeol, oleanolic acid, 3β-hydroxy-urs-11-en-28,13β-lactone (4), the mixture of α- and β-amyrin, trans-polyisoprene, and β-sitosterol were isolated from the leaves of Maytenus phyllanthoides. The structures of the isolated compounds were established based on spectroscopic data, mainly ¹H and 13C nuclear magnetic resonance (NMR). Compound 1, its acetate analog 1a, and compounds 2, 3, and 4 were tested against Trichomonas vaginalis. (+)-Lyoniresinol showed activity corresponding to IC50 17.57 µM. This is the first report on the occurrence of 3β-hydroxy-urs-11-en-28,13β-lactone (4) in the Celastraceous family and lyoniresinol in the Maytenus genus, and on the antitrichomonal activity of lyoniresinol.

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In addition to β-sitosterol, stigmasterol, phaeophitin A, luteolin, kaempferol, quercetin, (+)-catechin, quercetin-3-O-α-L-rhamnopyranoside, rutin, and p-hydroxy-benzoic acid, six known sesquiterpenes, namely (rel)-2β,6β-epoxy-5β-hydroxy-isodaucane, oplopanone, 1β,6α-dihydroxy-4(15)-eudesmene, caryophyllene oxide, α-cadinol, and spathulenol, were isolated from the leaves of Pterodon pubescens (Leguminosae) growing in the Cerrado of Mato Grosso do Sul, Brazil. The (rel)-2β,6β-epoxy-5β-hydroxy-isodaucane corresponds to the correct structure of homalomenol D. The sesquiterpene oplopanone, which bears a modified cadinane skeleton, is being reported for the first time in this genus. The structures of the compounds were determined on the basis of spectral data (MS, IR, and NMR-1D and 2D) and subsequent comparison with data reported in the literature.

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This is a description of the new species Mycovellosiella robsii, a cercosporoidal hyphomycete, associated with leaf spots on Mimosa caesalpiniaefolia, an important hedge plant with multiple uses in Brazil. The new species was compared to other cercosporoid species associated with plants of the genus Mimosa and other species of the genus Mycovellosiella described on legumes, and is recognized as a distinct taxon. Koch's postulates were carried out and the disease was reproduced by inoculating healthy plants with mycelial suspension or disk, confirming the pathogenicity. This is the first report of a fungal disease on this host.