980 resultados para Adams, Sarah Flower, 1805-1848.
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v.3,c.1 Pl
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2
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The influence of density of planting on flower production of carnation plants grown in vinil houses, was studied. Planting densities of 233,333; 175,000 and 116,667 plants per hectare were obtained by using planting spacings of 0.20 m between rows and 0.15 m, 0,20 m and 0.30 m between plants. Data were taken on total number of flowers per plant and per hectare. As far as planting densities are concerned, there was an increase of total flower production per hectare and a decrease of slower production per plant.
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v.51:no.3(1967)
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Based on the types of Edessa rufomarginata (De Geer, 1773) and its synonyms, on morphology of the paramere and coloration, seven patterns are described for E. rufomarginata. Pentatoma furcata Palisot de Beauvois, 1805, Cimex cruentus Fabricius, 1775, Aceratodes flavovirens Stål, 1855 and A. flavomarginatus Stål, 1855 are mantained as junior synonyms of E. rufomarginata. A. albomarginatus Stål, 1855 and A. marginalis Dallas, 1951 are removed from the synonymy of E. rufomarginata and are reinstated in Edessa. Aceratodes discolor Dallas, 1951 is removed from the synonymy of E. rufomarginata and is considered junior synonym of Edessa abdominalis Erichson, 1848.
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no.5(1924)
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Utilizando a microscopia ótica (MO) e eletrônica de varredura (MEV) procurou-se fornecer dados a taxionomia através da estrutura dos ovos e morfologia das ninfas, destes vetores da doença de Chagas. Os ovos em MO apresentam a superfície exocorial do opérculo e do corpo dividida em áreas poligonais com ornamentação própria; em T. maculata o exocório do corpo tem áreas indefinidas. Em MEV o exocório dos opérculos apresenta áreas poligonais de superfície estofada com pequena sulcos irregulares e perfurações distribuídas aleatoriamente nas duas espécies. O exocório do corpo apresenta: em T. maculata áreas acolchoadas com perfurações mais numerosas nos bordos, visualizando-se a borda corial, goteira espermática, aerópilas e micrópilas; em T. pseudomaculata as áreas são planas com numerosas perfurações. Nas ninfas o sulco estridulatório e o rostro apresentam diferenças significativas. O sulco estridulatórios em MO possibilitou diferenciar ninfas de 1º, 2º e 3º estádios, os 4º e 5º estádios apresentam-se semelhantes. Em MEV a diferenciação é acentuada. O rostro em MO apresenta pilosidade característica a partir do 3º estádio. T. maculata apresenta pêlos curtos e esparsos no 1º e 2º artículos e longos e numerosos no 3º, em T. pseudo-maculata semelhantes, porém mais curtos no 3º artículo.
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The behavioral response of Biomphalaria straminea to light was evaluted in terms of location of the snail in a Y-shaped aquarium in a situation of selection and of the rate (cm/hour) and direction of locomotion under homogeneous 9vertical) or differential (horizontal) lighting upon only one arm of the aquarium. The light source consisted of daylight fluorescent lamps with a spectrum close to that of natural light, with illumination varying from 28 to 350 lux. Analysis of the data showed that all animals, whether in groups or isolated, were attracted to light, although the time needed to approach the light source was 50% shorter for the former than for the latter. The rate of locomotion of B. straminea was 35% higher than observed in B. glabrata and 51% higher than that observed in B. tenagophila studied under similar conditions. The results are discussed in terms of social factors and geographical distribution of the three species.
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The different climatic regions determine the zoogeographic distribution of various animal species depending on their particular conditions and ecological preferences. The host schistosomiasis planorbid is one of these species. This paper deals with the distribution of Biomphalaria straminea in northeast Brazil. It starts from the analysis of different climatic peculiarities in this region, associated to limnological observation done by the author in three different hydric collections in the state of Sergipe. It has been concluded that this is an "eurióioca" species. Its broad ecological valence permits this species to survive in regions where climate asperties are evident, requiring behavior and physiological adaptations. The species survives in all northeast region, from "zona da mata", in the coast, to the semi-arid "sertão".