88 resultados para material flow.


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OBJECTIVE - To evaluate the Coronary Flow Reserve in the Coronary Sinus through transesophageal Doppler echocardiography in normal subjects. METHODS - We obtained technically adequate flow samples for analysis in 10 healthy volunteers (37±8 years, 5 men) with no history of heart or systemic disease and with mean left ventricular mass index by transthoracic echocardiography of 87±18 g/m². Coronary sinus flow velocity was recorded within the coronary sinus with the patient in a resting condition and during intravenous adenosine infusion at a dose of 140 µg/kg/min for 4 minutes. Recording of coronary sinus blood flow was possible in all cases with measurement of peak systolic, diastolic, and retrograde velocities (PSV, PDV, and PRV, cm/sec), mean systolic and diastolic velocities (MSV and MDV, cm/sec), and systolic and diastolic velocity time integral (VTI S and VTI D, cm/sec). RESULTS - The coronary flow reserve was calculated as the ratio between the blood flow in the basal state and the maximum measured hyperemic blood flow with adenosine infusion. Results are shown as mean and standard deviations. (CFR = PSV + PDV -- PRV/basal PSV): 1st min = 2.2±0.21; 2nd min = 3±0.3; 3rd min = 3.4±0.37; 4th min = 3.6 ± 0.33. CONCLUSION - Although coronary sinus flow had significantly increased in the first minute, higher velocities were seen at third and fourth minutes, indicating that these should be the best times to study coronary sinus flow with intravenous adenosine in continuous infusion.

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AbstractBackground:The relationship between psychiatric illness and heart disease has been frequently discussed in the literature. The aim of the present study was to investigate the relationship between anxiety, depression and overall psychological distress, and coronary slow flow (CSF).Methods:In total, 44 patients with CSF and a control group of 50 patients with normal coronary arteries (NCA) were prospectively recruited. Clinical data, admission laboratory parameters, and echocardiographic and angiographic characteristics were recorded. Symptom Checklist 90 Revised (SCL-90-R), Beck Depression Inventory (BDI), and Beck Anxiety Inventory (BAI) scales were administered to each patient.Results:The groups were comparable with respect to age, sex, and atherosclerotic risk factors. In the CSF group, BAI score, BDI score, and general symptom index were significantly higher than controls (13 [18.7] vs. 7.5 [7], p = 0.01; 11 [14.7] vs. 6.5 [7], p = 0.01; 1.76 [0.81] vs. 1.1[0.24], p = 0.01; respectively). Patients with CSF in more than one vessel had the highest test scores. In univariate correlation analysis, mean thrombolysis in myocardial infarction (TIMI) frame counts were positively correlated with BAI (r = 0.56, p = 0.01), BDI (r = 0.47, p = 0.01), and general symptom index (r = 0.65, p = 0.01). The psychiatric tests were not correlated with risk factors for atherosclerosis.Conclusion:Our study revealed higher rates of depression, anxiety, and overall psychological distress in patients with CSF. This conclusion warrants further studies.

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A more or less detailed study of the spermatogenesis in six species of Hemiptera belonging to the Coreid Family is made in the present paper. The species studied and their respective chromosome numbers were: 1) Diactor bilineatus (Fabr.) : spermatogonia with 20 + X, primary spermatocytes with 10 + X, X dividing equationaliv in the first division and passing undivided to one pole in the second. 2) Lcptoglossus gonagra (Fabr.) : spermatogonia with 20 + X, primary spermatocytes with 10 + X, X dividing equationally in the first division and passing undivided to one pole in the second. 3) Phthia picta (Drury) : spermatogonia with 20 + X, primary spermatocytes with 10 + X, X dividing equationally in the first division and passing undivided to one pole in the second. 4) Anisocelis foliacea Fabr. : spermatogonia with 26 + X fthe highest mumber hitherto known in the Family), primary .spermatocytes with 13 + X, X dividing equationally in the first division an passing undivided to one pole in the second. 5) Pachylis pharaonis (Herbtst) : spermatogonia with 16 + X, primary spermatocytes with 8 + X. Behaviour of the heteroehromosome not referred. 6) Pachylis laticornis (Fabr.) : spermatogonia with 14 + X, primary spermatocytes with 7 + X, X passing undivided to one pole in the first division and therefore secondary spermatocytes with 7 + X and 7 chromosomes. General results and conclusions a) Pairing modus of the chromosomes (Telosynapsis or Farasynapsis ?) - In several species of the Coreld bugs the history of the chromosomes from the diffuse stage till diakinesis cannot be follewed in detail due specially to the fact that lhe bivalents, as soon as they begin to be individually distinct they appear as irregular and extremely lax chromatic areas, which through an obscure process give rise to the diakinesis and then to the metaphase chomosomes. Fortunately I was able to analyse the genesis of the cross-shaped chromosomes, becoming thus convinced that even in the less favorable cases like that of Phthia, in which the crosses develop from four small condensation areas of the diffuse chromosomes, nothing in the process permit to interpret the final results as being due to a previous telosynaptic pairing. In the case of long bivalents formed by two parallel strands intimately united at both endsegments and more or less widely open in the middle (Leptoglossus, Pachylis), I could see that the lateral arms of the crosses originate from condensation centers created by a torsion or bending in the unpaired parts of the chromosomes In the relatively short bivalents the lateral branches of the cross are formed in the middle but in the long ones, whose median opening is sometimes considerable, two asymetrical branches or even two independent crosses may develop in the same pair. These observations put away the idea of an end-to-end pairing of the chromosomes, since if it had occured the lateral arms of the crosses would always be symetrical and median and never more than two. The direct observation of a side- toside pairing of the chromosomal threads at synizesis, is in foil agreement with the complete lack of evidence in favour of telosynapsis. b) Anaphasic bridges and interzonal connections - The chromosomes as they separate from each other in anaphase they remain connected by means of two lateral strands corresponding to the unpaired segmenas observed in the bivalents at the stages preceding metaphase. In the early anaphase the chromosomes again reproduce the form they had in late diafcinesis. The connecting threads which may be thick and intensely coloured are generally curved and sometimes unequal in lenght, one being much longer than the other and forming a loop outwardly. This fact points to a continuous flow of chromosomal substance independently from both chromosomes of the pair rather than to a mechanical stretching of a sticky substance. At the end of anaphase almost all the material which formed the bridges is reduced to two small cones from whose vertices a very fine and pale fibril takes its origin. The interzonal fibres, therefore, may be considered as the remnant of the anaphasic bridges. Abnormal behaviour of the anaphase chromosomes showed to be useful in aiding the interpretation of normal aspects. It has been suggested by Schrader (1944) "that the interzonal is nothing more than a sticky coating of the chromosome which is stretched like mucilage between the daughter chromosomes as they move further and further apart". The paired chromosomes being enclosed in a commom sheath, as they separate they give origin to a tube which becomes more and more stretched. Later the walls of the tube collapse forming in this manner an interzonal element. My observations, however, do not confirm Schrader's tubular theory of interzonal connections. In the aspects seen at anaphase of the primary spermatocytes and described in this paper as chromosomal bridges nothing suggests a tubular structure. There is no doubt that the chromosomes are here connected by two independent strands in the first division of the spermatocytes and by a single one in the second. The manner in which the chromosomes separate supports the idea of transverse divion, leaving little place for another interpretation. c) Ptafanoeomc and chromatoid bodies - The colourabtlity of the plasmosome in Diactor and Anisocelis showed to be highly variable. In the latter species, one may find in the same cyst nuclei provided with two intensely coloured bodies, the larger of which being the plasmosome, sided by those in which only the heterochromosome took the colour. In the former one the plasmosome strongly coloured seen in the primary metaphase may easily be taken for a supernumerary chromosome. At anaphase this body stays motionless in the equator of the cell while the chromosomes are moving toward the poles. There, when intensely coloured ,it may be confused with the heterochromosome of the secondary spermatocytes, which frequently occupies identical position in the corresponding phase, thus causing missinterpretation. In its place the plasmosome may divide into two equal parts or pass undivided to one cell in whose cytoplasm it breaks down giving rise to a few corpuscles of unequal sizes. In Pachylis pharaonis, as soon as the nuclear membrane breate down, the plasmosome migrates to a place in the periphery of the cell (primary spermatocyte), forming there a large chromatoid body. This body is never found in the cytoplasm prior to the dissolution of the nuclear membrane. It is certain that chromatoid bodies of different origin do exist. Here, however, we are dealing, undoubtedly, with true plasmosomes. d) Movement of the heterochromosome - The heterochromosome in the metaphase of the secondary spermatocytes may occupy the most different places. At the time the autosomes prient themselves in the equatorial plane it may be found some distance apart in this plane or in any other plane and even in the subpolar and polar regions. It remains in its place during anaphase. Therefore, it may appear at the same level with the components of one of the anaphase plates (synchronism), between both plates (succession) or between one plate and tbe pole (precession), what depends upon the moment the cell was fixed. This does not mean that the heterochromosome sometimes moves as quickly as the autosomes, sometimes more rapidly and sometimes less. It implies, on the contrary, that, being anywhere in the cell, the heterochromosome m he attained and passed by the autosomes. In spite of being almost motionless the heterochromosome finishes by being enclosed in one of the resulting nuclei. Consequently, it does move rapidly toward the group formed by the autosomes a little before anaphase is ended. This may be understood assuming that the heterochromosome, which do not divide, having almost inactive kinetochore cannot orient itself, giving from wherever it stays, only a weak response to the polar influences. When in the equator it probably do not perform any movement in virtue of receiving equal solicitation from both poles. When in any other plane, despite the greater influence of the nearer pole, the influence of the opposite pole would permit only so a slow movement that the autosomes would soon reach it and then leave it behind. It is only when the cell begins to divide that the heterochromosome, passing to one of the daughter cells scapes the influence of the other and thence goes quickly to join the autosomes, being enclosed with them in the nucleus formed there. The exceptions observed by BORING (1907) together with ; the facts described here must represent the normal behavior of the heterocromosome of the Hemiptera, the greater frequency of succession being the consequence of the more frequent localization of the heterochromosome in the equatorial plane or in its near and of the anaphase rapidity. Due to its position in metaphase the heterochromosome in early anaphase may be found in precession. In late anaphase, oh the contrary ,it appears almost always in succession. This is attributed to the fact of the heterochromosome being ordinairily localized outside the spindle area it leaves the way free to the anaphasic plate moving toward the pole. Moreover, the heterochromosome being a round element approximately of the size of the autosomes, which are equally round or a little longer in the direction of the movement, it can be passed by the autosomes even when it stands in the area of the spindle, specially if it is not too far from the equatorial plane. e) The kinetochore - This question has been fully discussed in another paper (PIZA 1943a). The facts treated here point to the conclusion that the chromosomes of the Coreidae, like those of Tityus bahiensis, are provided with a kinetochore at each end, as was already admitted by the present writer with regard to the heterochromosome of Protenor. Indeed, taking ipr granted the facts presented in this paper, other cannot be the interpretation. However, the reasons by which the chromosomes of the species studied here do not orient themselves at metaphase of the first division in the same way as the heterochromosome of Protenor, that is, with the major axis parallelly to the equatorial plane, are claiming for explanation. But, admiting that the proximity of the kinetochores at the ends of chromosomes which do not separate until the second division making them respond to the poles as if they were a single kinetochore ,the explanation follows. (See PIZA 1943a). The median opening of the diplonemas when they are going to the diffuse stage as well as the reappearance of the bivalents always united at the end-segments and open in the middle is in full agreement with the existence of two terminal kinetochores. The same can be said with regard to the bivalents which join their extremities to form a ring.

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O presente trabalho descreve a técnica de separação de cátions e ânions de solução pura, contendo os principais íons que ocorrem em material vegetal, mediante o emprego de coluna de resina trocadora de cátions Dowex 50 - X8. Foram estudados o efeito do pH na retenção dos cátions, a eluição destes e a sua recuperação, a lavagem da coluna de resina e a recuperação dos ânions. Mediante os resultados obtidos, foi possível estabelecer condições para o emprego da citada técnica na separação de cátions e ânions em extratos provenientes de material vegetal.

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Bulbos de 2° ciclo, tipo jumbo, com 84 g/unidade e tipo 1, com 35 g/unidade, foram comparados. Verificou-se que: o tipo jumbo teve melhor rendimento de: peso de bulbos; número de bulbos; comprimento da haste floral; comprimento da espiga floral e hastes florais de melhor qualidade. Otipo 1 apresentou melhor rendimento para peso de bulbos plantados por peso de bulbos e cormilhos colhidos.

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Bulbos de mesmo ciclo, com pesos e tamanhos próximos, apresentaram comportamentos semelhantes para a produção de flores, bulbos e cormilhos. Os bulbos maiores, tipos 1 e 2, tiveram melhor rendimento de flores, bulbos e cormilhos que os demais tipos, decrescendo esse rendimento com a redução do tamanho dos bulbos por unidade plantada. Em função do peso plantado, as unidades menores apresentaram melhor desempenho.

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Foi conduzido um ensaio numa plantação comercial de café de variedade Mundo Novo de 9 anos de idade, com uma população de 1904 covas/ha, destinada a avaliar a quantidade de biomassa e de nutrientes removidas por diferentes tipos de poda: recepa a 0,40m; decote a 1,00, 1,50 e 2,00 m; decote a 1,50m com esqueletamento. A análise do material e dos dados permitiu tirar-se as seguintes conclusões: (1) a biomassa removida pela poda foi maior na recepa (24,3 t de matéria fresca e 11,9 de matéria seca) e no decote a 1,00 m (20,6 e 10,1 t, respectivamente); seguia-se o decote a 1,50 m com esqueletamento que deu 19,4 e 8,3 t de matéria fresca e seca por hectare; os pesos da matéria fresca e seca correspondentes aos decotes a 1,50 m e 2,00 m foram: 12,1 e 5,4; 5,6 e 2,5 t/ha; (2) a relação existente entre a altura de poda e quantidade de fitomassa removida é descrita por equações de regressão simples; (3) as quantidades de nutrientes removidas são proporcionais as quantidades de material podado sendo as seguintes de acordo com a ordem dos tratamentos dado, em kg/ha: N - 320, 294, 162, 80 e 261; P - 18, 15, 10, 44 e 16; K - 286, 266, 168, 78 e 273; Ca - 149, 139, 63, 33 e 101: Mg - 30, 33, 16, 8 e 26; S - 10, 7,6, 3 e 10; as quantidades de micronutrientes removidas foram, em g/ha: B - 306, 337, 163, 83 e 268; Cu - 229, 219, 121, 51 e 191; Fe - 2783, 2328, 1367, 544 e 2,088; Mn - 437, 779, 264, 142 e 412; Zn - 174, 152, 74, 28 e 121; (3) foram derivadas equações de regressão simples que relacionam quantidade extraídas e altura da poda; (4) a reciclagem de fitomassa contribui com economia substancial de fertilizantes para a nova vegetação. Cerca de dois terços e três quartos de nutrientes, entretanto, estão contidos no material lenhoso de caules e ramos o que deve fazer que a sua disponibilidade seja mais lenta.

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A região da Serra da Onça é localizada no nordeste do Estado de Minas Gerais, no vale formado pelos trabalhos dos rios São Francisco e seus afluentes Jequitaí e Rio das Velhas. Esta região é caracterizada por diversos ciclos erosivos. Uma topossequência representativa da área foi escolhida para este estudo, sendo constituida por 5 perfis de solos desenvolvidos de sedimentos Quaternários. 0 Perfil 1, um Typic Hapleustox, está localizado na superfície mais antiga. Os outros solos estão localizados no sedimento Holocênico, área aluvial do São Francisco. Estes solos são menos intemperizados e classificados como Plíntic Haplustult (Perfil 2), Oxic Plintaquult (Perfil 3); Fluventic Plinthustult (Perfil 4) e Fluventic Argiustol (Perfil 5). Análises mineralógicas foram efetuadas em todas as fraçõs do solo. O Perfil 1 apresenta, em sua fração areia, somente minerais resistentes ao intemperismo, enquanto que nos demais solos, menos intemperizados, ocorrem micas e plagioclásios. Tais minerais aumentam de acordo com a profundidade do solo e também do Perfil 1 ao Perfil 5 menos intemperizado. A caulinita é o mineral de argila dominante na fração argila de todos os solos estudados, com maior concentração no Perfil 1, mais intemperizado. Este mineral tende a decrescer em profundidade e na direção do Perfil 1. Micas, vermiculita e montmorilonita também ocorrem do Perfil 2 ao Perfil 5.

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É estudado o relacionamento entre a fisiografia e os solos evoluídos a partir de sedimentos cenozóicos, de textura e composição variáveis, depositados sob a ação do rio São Francisco e tributários. A região (vale do rio Jequitai, MG) é caracterizada por um clima sub-úmido, onde o regime de umidade do solo é ústico e o de temperatura isotérmico. Foram coletados 5 pedons dispostos numa topossequência. Na posição mais antiga (pleistocênica), o solo apresenta-se em um estágio de intensa alteração (Typic Haplustox). Os demais solos encontram-se sobre sedimentos holocênicos, compondo a planície aluvial do rio São Francisco e são, mineralogicamente, mais jovens, com horizonte argílico, representado por ultissol e molissol, ocorrência esta pouco comum em situações de planície aluvial recente. No pedon 1 (Typic Haplustox), os minerais primários intemperizáveis inexistem na fração grosseira. O pedon 2 (Plinthic Haplustult) apresenta na fração areia um acréscimo em profundidade de minerais de fácil alteração. Na fração silte, os feldspatos já estão em fase de alteração. Os pedons 3 (Oxic Plintaquult), 4 (Fluventic Plinthustult) e 5 (Fluventic Argiustol) mostram elevadas proporções de minerais primários de fácil alteração (placioclásios calco-sódicos, hornblenda), principalmente nas frações areia e silte. A ocorrência destes minerais associa-se a um processo deposicional recente, aliado às condições de clima e drenagem locais.

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The type material of Phasmatodea deposited in Brazilian museums and institutions is listed for the first time. New synonyms are proposed: Phibalosoma paulense Toledo Piza, 1938, Phibalosoma rochai Toledo Piza, 1938, Bacteria tuberculata Toledo Piza, 1938 and Bacteria tuberculata var. argentina Toledo Piza, 1938 are junior synonyms of Cladomorphus phyllinus (Gray, 1835). Nineteen new combinations are established.

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Repetimos não desejar tirar conclusões de um material histopatológico procedente de necrópsias e biópsias de doentes com afecções diversas. Todavia, podemos admitir o seguinte: 1. Tem-se a impressão de que nos portadores de neoplasias malignias, o número de megacariócitos presentes na medula óssea é elevado; no pulmão é regular, dependente da megacariocitopoiese medular. 2 Não foi possível identificar nenhum megacariócito nos outros órgãos por nós estudados, procedentes dêstes mesmos doentes, parecendo, portanto, que não exitirá uma megacariocitopoiese extramedular nos adultos. Os megacariócitos procedentes de medula, por ser células muito volumosas, serão retidas em sua maior parte pelo pulmão, pois é o órgão que recebe tôda a circulação venosa. 3. Quanto à citologia cabe assinalar que, no grupo formado por indivíduos portadores de neoplasias malignas, os megacariócitos de medula óssea apresentam-se bem conservados, morfològicamente normais, bi ou polilobulados, porém maiores e às vezes com formas bizarras. No pulmão, são geralmente de formas alongadas ou bizarras, com núcleos densos, picnóticos e com o citoplasma reduzido a uma fina camada periférica.