984 resultados para Embryo diagnose


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Com os teores foliares de N, P e K (+3) obtidos em amostragens sucessivas e a quantidade de chuvas que caem nos 2 meses anteriores, foram calculadas as equações de regressão correspondentes. Em seguida, foi possível determinar o aumento esperado nos níveis de P e K para 200 mm de chuva, dentro de sessenta dias antes da amostragem.

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Com os teores de Ca, Mg e S na folha (+3), obtidos em amostragens sucessivas, e a quantidade de chuvas que caem nos sessenta dias anteriores, foram calculadas as equações de regressão correspondentes. Em seguida, foi possível determinar a variação esperada nos níveis de Mg para 200 mm de precipitação 2 meses antes da amostragem.

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Usando-se os teores de N, P e K de folha +3 encontradas em amostragens sucessivas e a quantidade de chuvas que caiu nos 2 meses anteriores, foram calculadas as equações de regressão correspondentes. Em seguida, calculou-se o aumento esperado nos teores de N e P devido a queda de 200 mm de chuva 2 meses antes da amostragem.

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Os teores de Ca, Mg e S da folha +3 encontrados em amostragens sucessivas e a quantidade de chuvas que caiu nos 2 meses anteriores foram usados no cálculo de correlação entre as duas variáveis e no estabelecimento de equações de regressão. Em seguida foram calculadas os aumentos esperados nos níveis foliares de Mg e S em função de 200 mm de precipitação, sessenta dias antes da amostragem.

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Os efeitos da aplicação de cinco níveis de calcário dolomítico (0 - 1,25 - 2,50-5,00 e 10,00 t/ha) foram estudados em um Latossol Vermelho Escuro textura média. A calagem aumentou a produção de colmos de sorgo sacarino, sendo que as produções mais elevadas foram obtidas quando a soma de cálcio e magnésio, saturação em bases e valor pH do solo eram, respectivamente, 2,93 meq/100 cm³, 59% e 5,71. Foram observados desequilíbrios na nutrição potássica com a aplicação de 10 t/ha de calcário dolomítico. Os níveis críticos de Mg nas folhas + 4e + 3, coletadas, respectivamente, aos 45e 83 dias, foram 0,19 e 0,31% A qualidade do caldo não foi alterada significativamente pelas doses de calcário dolomítico empregadas.

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RESUMO As espécies de Histeridae são quase que exclusivamente predadoras e podem ser encontradas em uma grande diversidade de ambientes. Dentre os grupos associados a carcaças, alguns são citados como relevantes na entomologia forense médico-legal. Entretanto, há pouca informação taxonômica para a família, principalmente na Região Neotropical. Desta forma, os objetivos do trabalho foram elaborar uma chave de identificação e caracterizar as espécies de Histeridae de interesse médico-legal no Brasil. Além disso, são apresentadas informações de distribuição geográfica e aspectos biológicos das espécies. As seguintes espécies são registradas como relevantes na entomologia forense no Brasil: Aeletes nicolasi Leivas, 2012; Euspilotus azureus (Sahlberg, 1823); Hister cavifronsMarseul, 1854; Omalodes bifoveolatus Marseul, 1853;Omalodes foveola Erichson, 1834; Omalodes lucidus Erichson, 1834, Operclipygus subterraneusCaterino & Tishechkin, 2013; Phelister sanguinipennisMarseul, 1853; e Scapomegas auritus Marseul, 1855. Esta contribuição representa a primeira ferramenta para uma melhor identificação dos Histeridae associados a carcaças no Brasil e pode servir como referência e aplicação na entomologia médico-legal.

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Current in vitro fertilisation (IVF) practice requires synchronisation between the¦environment of cultured oocytes and embryos and the surroundings to what they would have¦been exposed to in vivo. Commercial, sequential media follow this requirement but their exact¦composition is not available. We have compared two widely used IVF culture media systems using¦the two choriocarcinoma cell lines JEG-3 and BeWo. The two hormones hCG and progesterone¦were determined in the culture supernatants as endpoints. In both cell lines, but in a more¦pronounced way in JEG-3, progesterone rather than hCG production was stimulated, and a¦higher hormone release was observed in the fertilisation than in the cleavage media. Differences¦between manufacturers were small and did not favour one system over the other. We conclude¦that both sequential media systems can be equally well used in current IVF laboratory practice.¦© 2012 Elsevier Masson SAS. All rights reserved.

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Oxygen uptake was studied during the establishment of cephalocaudal polarity in the very early chick embryo, i.e., 10 hr before (stage VI) and at laying (stage X). Oxygen fluxes in minute regions of the intact blastoderms were measured in vitro by scanning microspectrophotometry in the presence or absence of glucose. The oxygen consumption of the whole blastoderm remained constant (6 nmol O2 X hr-1) throughout the period studied, although the number of cells increased more than twofold. The regional oxygen fluxes varied from 0.41 to 1.13 nmol O2 X hr-1 X mm-2 at stage VI and from 0.42 to 0.70 nmol O2 X hr-1 X mm-2 at stage X. At stage VI, the oxygen flux in the center of the blastoderm was significantly higher than that in its periphery. This pattern remained evident when the values were corrected for cell number or for cytoplasmic volume. At stage X, there was a tendency for the oxygen fluxes to decrease from the posterior to the anterior regions of the area pellucida. Thus the pattern of oxidative metabolism in the late uterine embryos seems to change from radial to bilateral. This change of symmetry probably reflects the process of formation of the embryonic axis. In addition, the fact that the oxygen uptake was similar in the presence or absence of glucose suggests that early chick embryos metabolize essentially intracellular stores.

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Effects of insulin upon glucose metabolism were investigated in chick embryos explanted in vitro during the first 30 h of incubation. Insulin stimulated the glucose consumption of the chick gastrula (18 h) and neurula (24 h), but had no effect on the late blastula (0 h:laying) and on the stage of six to eight somites (30 h). The increase in glucose consumption concerned both the embryonic area pellucida (AP) and extraembryonic area opaca (AO). AP responded to a greater extent (50%) and at a lower range of concentrations (0.1-1.0 ng/ml) than AO (30%; 1-100 ng/ml). Insulin had no effect on the oxygen consumption of blastoderms, whereas it stimulated the aerobic lactate production (approximately 70% of the additional glucose consumption was converted to lactate). The nanomolar range of stimulating concentrations suggests that insulin has a specific effect in the chick embryo, and that it could modulate glucose metabolism in ovo as well. The transient sensitivity of the embryo to insulin is discussed in relation to behavior of mesodermal cells.

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Mating with attractive or dominant males is often predicted to offer indirect genetic benefits to females, but it is still largely unclear how important such non-random mating can be with regard to embryo viability. We sampled a natural population of adult migratory brown trout (Salmo trutta), bred them in vitro in a half-sib breeding design to separate genetic from maternal environmental effects, raised 2098 embryos singly until hatching, and exposed them experimentally to different levels of pathogen stress at a late embryonic stage. We found that the embryos' tolerance to the induced pathogen stress was linked to the major histocompatibility complex (MHC) of their parents, i.e. certain MHC genotypes appeared to provide better protection against infection than others. We also found significant additive genetic variance for stress tolerance. Melanin-based dark skin patterns revealed males with 'good genes', i.e. embryos fathered by dark coloured males had a high tolerance to infection. Mating with large and dominant males would, however, not improve embryo viability when compared to random mating. We used simulations to provide estimates of how mate choice based on MHC or melanin-based skin patterns would influence embryos' tolerance to the experimentally induced pathogen stress.

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We have previously shown that neuroblasts from cerebral hemispheres of 6-day-old chick embryos are able to proliferate when grown in the presence of fetal calf serum. We report here that in the presence of horse serum alone the proliferative rate of neuroblasts is strongly reduced. A high proliferative rate is restored upon the addition of bovine transferrin and to a lesser extent with added FeSO4 or hemin. These findings suggest that the transferrin of horse serum cannot be used by chick neuroblasts in vitro, while bovine transferrin exogenously added is active in promoting cell proliferation. We propose that the stimulatory activity of the fetal calf serum is due to bovine transferrin, since when this serum is fractionated by gel filtration, the fractions that stimulate the proliferation of neuroblasts grown in the presence of horse serum are located in the molecular weight area of transferrin, and they do contain transferrin as seen by immunoblotting with a specific anti-transferrin antibody.

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The present paper reviews our recent data concerning the use of immunological methods employing monoclonal antibodies and synthetic peptides to study malaria transmission and immunity and to diagnose plasmodial infection. As concerns malaria transmission, we studied the main vectors of human malaria and the plasmodial species transmitted in endemic areas of Rondônia state, Brazil. The natural infection on anopheline was evaluated by immunoradiometric assay (IRMA) using monoclonal antibodies to an immunodominant sporozoite surface antigen (CS protein) demonstrated to be species specific. Our results showed that among six species of Anopheles found infected, An. darlingi was the main vector transmitting Plasmodium falciparum and P. vivax malaria in the immediate vicinity of houses. In order to assess the level of anti-CS antibodies we studied, by IRMA using the synthetic peptide corresponding to the repetitive epitope of the sporozoite CS protein, sera of individuals living in the same areas where the entomological survey has been performed. In this assay the prevalence of anti-CS antibodies was very low and did not reflect the malaria transmission rate in the studied areas. In relation to malaria diagnosis, a monoclonal antibody specific to an epitope of a 50 kDa exoantigen, the major component of supernatant collected at the time of schizont rupture, was used as a probe for the detection of P. falciparum antigens. This assay seemed to be more sensitive than parasitological examination for malaria diagnosis since it was able to detect plasmodial antigens in both symptomatic and asymtomatic individuals with negative thick blood smear at different intervals after a last parasitologically confirmed confirmed attack of malaria.