678 resultados para Sacharopolyspora spinosa


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Searching for a new alternative to A. diaperinus control, it was evaluated the action of Spinosad in two concentrations (250ppm, 400ppm) and two doses (0.05 L/m 2 and 0.1 L/m 2), applied in poultry broiler facilities naturally infested by this coleoptera. Assessments of the infestation were held in weekly intervals, during 49 days after treatment, using traps. The percentage of effectiveness were calculated from the results of the number of adults and/or larval stages in control and treated groups. Spinosad at the concentration of 250ppm, applied at a dose of 0.1L/m2, can be considered ineffective against these beetles, however the application of 400ppm at a dose of 0.1L/m2 showed high efficacy and short residual period. The dose of 0.1L/m 22 of Spinosad at the concentration of 400ppm demonstrated, between treatments, better effectiveness against coleopters, reaching efficacy of 100% against larvae of A. diaperinus, observed after the seventh day post-treatment.

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Cleome spinosa é uma espécie herbácea de uso na medicina popular, especialmente no Nordeste do Brasil. A cultura in vitro de raízes adventícias da espécie foi iniciada com segmentos radiculares (0,5 e 1,0 cm) obtidos a partir de duas fontes de explantes: plantas propagadas in vitro e plantas oriundas do processo de germinação in vitro. Os explantes foram inoculados em meio MS líquido suplementado ou não com as auxinas ANA, AIA e AIB em diferentes concentrações (0,5; 1,0; 1,5; 3,0; 5,0 mg.L-1). As culturas foram mantidas em sala de crescimento, sob agitação (100 rpm) e sob fotoperíodo de 16h ou no escuro, com subculturas a cada 45 dias. Explantes oriundos de plantas propagadas in vitro também foram cultivados em meio contendo a citocinina BAP em associação com auxinas, na presença de sorbitol (isoladamente ou em associação com sacarose), em meio MS contendo redução na concentração total de sais minerais (MS1/2 e MS1/4) e em meio sólido. Os resultados mostraram que a adição de auxinas ao meio de cultura foi essencial à multiplicação das raízes, uma vez que em meio MS0 ocorreu significativo desenvolvimento de brotos. A suplementação com ANA não foi eficiente para a produção de raízes e acarretou no calejamento dos explantes, enquanto que a presença de AIA e AIB resultaram na multiplicação das raízes. Ainda assim, independentemente das manipulações realizadas no meio de cultivo, a capacidade de multiplicação mostrou-se reduzida. Uma expressiva multiplicação de raízes foi observada em culturas iniciadas a partir de explantes oriundos de plantas obtidas por germinação in vitro. A maior produção de biomassa foi alcançada em culturas iniciadas com segmentos radiculares de plantas obtidas por germinação in vitro cultivadas em meio contendo com 3,0 mg.L-1 de AIB e mantidas no escuro. Culturas estabelecidas nas melhores condições para acúmulo de biomassa foram acompanhadas por três subculturas, sendo avaliados períodos de cultura de 45 dias e de 60 dias. Culturas mantidas a intervalos de 45 dias apresentaram maior produção de raízes durante a segunda subcultura, enquanto que para o intervalo de 60 dias, embora tenha sido observada a capacidade de multiplicação das raízes, a maior produção de biomassa ocorreu nos primeiros 60 dias de cultivo. A partir de materiais in vivo e in vitro foram realizadas extrações com solventes de polaridade crescente (hexano, diclorometano, acetato de etila e metanol) e os extratos foram submetidos a avaliações cromatográficas. As análises por cromatografia em camada delgada mostraram a presença de terpenos nos extratos obtidos com hexano e diclorometano, tanto em material obtido a campo como naqueles produzidos in vitro e de compostos fenólicos nos extratos em acetato de etila obtidos a partir de material de campo. Pelas análises por cromatografia líquida associada à espectrometria de massas foi possível observar a presença de flavonoides nas culturas in vitro, não detectados no material de campo. As análises por cromatografia de fase gasosa associada à espectrometria de massas apontaram a presença de esteroides nos extratos em hexano de raízes coletadas a campo e nas culturas in vitro de raízes. Os resultados obtidos mostraram a viabilidade da produção de culturas de raízes in vitro para a espécie C. spinosa e o potencial deste material para a produção de substâncias bioativas, algumas não encontradas em material coletado a campo

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Se propone una representación de la distribución actual del endrino (Prunus spinosa L.) en Navarra. Para la canfección del mapa se dividió la superficie de Navarra según una malla cuadrada de 10 km. de lado. En cada cuadricula se realizaron recorridos detallados que permitieron conocer el grado de presencia de la especie estudiada.

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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In this present work an ethnographic research was performed with 84 native medicinal specimens from the Litoral Norte Riograndense, from which two plants Cleome spinosa Jacq e Pavonia varians Moric were submitted to ethnobotanic, phytochemistry and pharmacologic investigations. Additionally, a phytopharmacological research of the medicinal specimen Croton cajucara Benth ( native plant of the Amazon region of Brazil) was improved. The obtained phytochemical results of the C. spinosa and P. varians showed the presence of flavonoids constituents, among other components. The two flavonoids (2S)-5-hydroxy-7,4 -dimethoxy-flavanone and 5,4 -dihydroxy-3,7,3 -trimethoxy-flavone were isolated from C. spinosa. The antioxidant activity of the hydroalcoholic extracts of C. spinosa and P. varians solubilized in the microemulsion systems SME-1 and SME-4, was evaluated in the DPPHmethod. The used SME systems [obtained with Tween 80: Span 20 (3:1) and isopropyl myristate (IPM)] improved the dissolution of those tested polar extracts, with higher efficacy to the SME-1 system (in which ethanol was included as cosurfactant). The CE50 values evidenced for P. varians were 114 [g/mL (SME-1) and 246 [g/mL (SME-4); for C. spinosa it was 224 [g/mL (SME-1) and 248 [g/mL (SME-4), being the system SME-1 more effective for both tested extracts. The hydroalcoholic extracts of P. varians (HAE-PV) was also submitted to pharmacological screening for antinociceptive activity in animal models. The oral administration of this extract (100, 300 and 1000 mg/kg) inhibited the acetic acid-induced writhing in mice. The higher inhibition (74%) was evidenced to the 1000 mg/kg administered dose. Its effect on the central nervous system (CNS) was investigated by tail flick and formalin-method and reveled that it has negligible antinociceptive action on the CNS. After taking consideration of HAE-PV interaction, Pavonia varians Moric could be used as a potent analgesic agent in case of peripheral algesia, without affecting the CNS. The phytochemical study of the stem bark of Croton cajucara Benth lead to the isolation of 19-nor-clerodanetype diterpenes, as well as to the separation of its fixed oil FO-CC. This non polar oil material reveled to be rich in sesquiterpenes and 19-nor-clerodanes components. The biologic effect of OF-CC was evaluated in the development in vitro of the fungis phytopatogens such as Fusarium oxysporum, Rhizoctonia solani and Sclerotium rolfsii. Significant inhibitory effect of the tested fungis (at 0,2 mg.mL-1 dosage) were comproved. A Mass Spectrometry study of clerodane-type diterpenes was developed in order to identify characteristic fragments on mass spectrometra of both clerodane and 19-nor-clerodane presenting an α,β-insaturated carbonyl moiety at ring A of the decalin-system. For that study, mass spectroscopy data were analysed for 19-nor-clerodanes [trans-dehydrocrotonin (DCTN), trans-crotonin (CTN), cis-cajucarin B (c-CJC-B), and cajucarinolide (CJCR)] and for clerodanes [isosacacarin (ISCR) and transcajucarin A (t-CJC-A)] obtained from the stem bark of C. cajucara, and also clerodane-type from other species. The trans-junction of the enone-system clerodanes was clear correlated with the presence of the characteristic ions at m/z 95, 121 e 205. Meanwhile, the characteristics ions at m/z 122 e 124 were correlated to cis-junction. The trans-junction of the enone-system 19-nor-clerodanes showed characteristics ions at m/z 161, 134 e 121. This study could be successful employed for identification of clerodane constituents from other specimens without any additional spectroscopic analyses, as well as a previously phytochemical analyzes in clerodane project search

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The main goal of this study was the identification of the items of the diet of the L. spinosa, based on the stomach contents analysis. The crabs were obtained from Ubatuba region north-eastern shore of São Paulo State. In the laboratory, all the individuals were dissected, the stomach was retreated and fixed in 10% formaline. The alimentary items were identified under stereomicroscope and analysed by the method of Frequency of Occurrence. A total of 194 stomachs was analysed and nine alimentary items were obtained. Unindentified material was found in 98% of analysed stomach and poriferan were present in less then 1% of stomachs. These results pointed a diversified diet explored by this crab, as well as the employment of some different methods for food intake. This suggested that these crabs could occupy different position in the trophic chain.

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Aspectos morfológicos e anatômicos da folha de Jacaratia spinosa (Aubl.) A.DC. (Caricaceae) foram estudados com detalhe. O limbo foliar possui organização dorsiventral, estômago anomocíticos, glândulas, laticíferos do tipo articulado anastomosado e epiderme papilosa na face abaxial. A venação é bronquidódroma terminando em alças no bordo foliar.

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An iridoid glucoside: randinoside, along with five known iridoids: galioside, deacetylasperulosidic acid methyl ester, scandoside methyl ester, geniposide and gardenoside, were isolated from the stems of Randia spinosa. The structures were determined by spectroscopic analysis, including 2D NMR techniques. © 2003 Elsevier Science Ltd. All rights reserved.

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The objective of this study was to investigate the spatial and temporal distribution of Libinia spinosa H. MILNE EDWARDS 1834 on unconsolidated sublittoral bottoms in two regions off the northern coast of the state of São Paulo, and to analyze the influence of environmental factors on the occurrence of this species and observe the recruitment pattern of its young. Crabs were collected monthly (July 2001 through June 2003) at depths of 5, 10, 15, 20, 25, 30 and 35 In, from a fishing boat equipped with two double-rig nets. Samples of water and sediment were collected for analysis of environmental factors. A total of 2112 spider crabs was obtained (701 juveniles and 1411 adults). The highest abundance was observed at depths of 20 and 25 m, in both regions. These localities were characterized by substrate composed of very fine sand and silt-clay. In regard to the temporal distribution, juveniles and adults predominated in the summer and winter months respectively. From these results, one can infer that the distribution of L. spinosa is related to environmental factors favorable for its life cycle; sediment type is the factor which most strongly determines its presence. © E. Schweizerbart'sche Verlagsbuchhandlung (Nägele u. Obermiller), 2007.

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Libinia spinosa H. Milne Edwards in Guérin, 1832 and L. ferreirae Brito Capello, 1871, inhabit very similar environments, and their geographic and bathymetric distributions overlap for about 3000 km along the southwestern Atlantic. Both species are commonly caught in the same haul and differentiating between them can often be difficult. Traditionally, morphological differentiation between L. spinosa and L. ferreirae has been based exclusively on the number of spines along the median, longitudinal line of the carapace and the development of a process at the anterolateral angle of the basal segment of the antenna. Because Libinia spinosa and L. ferreirae share similar numbers of median spines (7 and 6, respectively), and the number of median spines of the carapace and the process at the anterolateral angle of the basal antennal segment are variable, they are of little value in separating these species. It is shown herein that unequivocal identification can be easily achieved based on features of the male and female thoracic sternum, pereiopod dactyli, and infraorbital notch. A lectotype is designated for L. spinosa and its authorship and date are corrected. Libinia gibbosa A. Milne-Edwards, 1878, is demonstrated to be a junior synonym of L. ferreirae. The holotype of L. gibbosa is figured for the first time.