8 resultados para Harris, Joseph.

em Scielo Saúde Pública - SP


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Este é o primeiro registro de Paravelia recens (Drake & Harris, 1935) (Heteroptera: Veliidae) em fitotelmata de Guzmania brasiliensis Ule, 1907 (Bromeliaceae). O estudo foi conduzido na Reserva Florestal Adolpho Ducke, localizada na rodovia AM 010 km 26, Manaus, Amazonas. Foram realizadas doze amostragens, entre abril de 2003 e abril de 2005, seis no período chuvoso e seis no período de seca. Para cada amostragem, 12 bromélias foram analisadas, seis terrestres e seis epífitas, totalizando 144 amostras. Com exceção das amostras de março e outubro de 2004, 94 espécimes de P. recens foram encontrados. O número de indivíduos coletados foi semelhante nos estratos amostrados, sendo 46 terrestres e 48 epífitas. No período chuvoso foi encontrado um maior número de P. recens (teste-t entre períodos; t =2,57; p=0,011), assim como a abundância de indivíduos esteve positivamente correlacionada com o volume de água por bromélia (r s= 0,18; p=0,033). Este fato pode ser explicado pelo maior aporte de água no período chuvoso acarretando o aumento do volume médio de água nas bromélias.

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Mesovelia mulsanti White, 1879 and M. zeteki Harris & Drake, 1941 are newly recorded in the Amazon River floodplain, Brazil. A key to the three known species ocurring in this region is also provided. Mesovelia mulsanti can be distinguished from M. amoena and M. zeteki by the body length larger than 2.50 mm, the head without longitudinal brown stripes near midline, and the forefemur and midfemur of the male, which have ventral rows of spines. Mesovelia amoena differs from M. zeteki in aspects of body color and in number of spinules near posterior margin of abdominal sternite VI of male.

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Com o intuito de elucidar a cosntituição da genitália masculina e criar novos parâmetros para serem usados em taxionomia, estudamos Limnogonus aduncus Drake & Harris, 1932 - Gerrinae e Halobatopsis platensis (Berg, 1879) - Trepobatinae, evidenciamenos 11 estruturas no falo e comprovamos uma nítida separação entre estas duas subfamílias, não só pela disposição como também pela forma do aparelho articular, vesica, falosoma, suporte do falosoma, conjuntiva e parâmetros.

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Objective: To investigate the neuromotor development of at-risk children between three and 12 months of life, administering the Brazilian version of the Harris Infant Neuromotor Test (HINT).Method: A longitudinal study, with 78 children and 76 parents/guardians discharged from a neonatal intensive care unit in Fortaleza-CE/Brazil. Two instruments were administered: HINT and a socioeconomic questionnaire, between July/2009 to August/2010. Data from 55 preterm and 23 term children were analyzed. Results: The final mean scores ranged from 14.6 to 25.2 and from 11.2 to 24.7, for preterm and term, respectively, showing that 91% of children demonstrated good neuromotor performance; seven premature infants showed alterations which led to the referral of three children to a specialized clinic for examination and diagnostics.Conclusion: The test allowed nurses to assess infant development, identify deviations early, and plan interventions.

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The second half of eighteenth century is marked by the advancement of chemistry and geology. The first science acquired the law of conservation of mass and this science represented a important support to geology and mineralogy. We say that both became modern science that time. Our aim is to show up some interrelations between history of chemistry and history of geology by means of the study of Joseph Black's and James Hutton's works. We defend that it is positive to science education to understand and approach the relations among different and disciplinary areas of science.

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Many students and professionals in chemistry and chemical engineering related the name Kwong with one of the most remarkable equations of state with two parameters. In the same way, very few people know who Kowng was. This article shows some of the unknown personal and professional facts of Joseph Neng Shun Kwong, a person who devoted almost four decades of his life to the industrial research in the adhesives industry.

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Machado-Joseph disease (MJD) is a form of autosomal dominant spinocerebellar ataxia first described in North-American patients originating from the Portuguese islands of the Azores. Clinically this disorder is characterized by late onset progressive ataxia with associated features, such as: ophthalmoplegia, pyramidal and extrapyramidal signs and distal muscular atrophies. The causative mutation is an expansion of a CAG repeat in the coding region of the MJD1 gene. We have identified 25 unrelated families segregating the MJD mutation during a large collaborative study of spinocerebellar ataxias in Brazil. In the present study a total of 62 family members were genotyped for the CAG repeat in the MJD1 gene, as well as 63 non-MJD individuals (126 normal chromosomes), used as normal controls. We observed a wide gap between the size range of the normal and expanded CAG repeats: the normal allele had from 12 to 33 CAGs (mean = 23 CAGs), whereas the expanded alleles ranged from 66 to 78 CAGs (mean = 71.5 CAGs). There were no differences in CAG tract length according to gender of affected individuals or transmitting parent. We observed a significant negative correlation between age at onset of the disease and length of the CAG tract in the expended allele (r = -0.6, P = 0.00006); however, the size of the expanded CAG repeat could explain only about 40% of the variability in age at onset (r2 = 0.4). There was instability of the expanded CAG tract during transmission from parent to offspring, both expansions and contractions were observed; however, there was an overall tendency for expansion, with a mean increase of +2.4 CAGs. The tendency for expansion appeared to the greater in paternal (mean increase of +3.5 CAGs) than in maternal transmissions (mean increase of +1.3 CAGs). Anticipation was observed in all transmissions in which ages at onset for parent and offspring were known; however, anticipation was not always associated with an increase in the expanded CAG repeat length. Our results indicate that the molecular diagnosis of MJD can be confirmed or excluded in all suspected individuals, since alleles of intermediary size were not observed.