38 resultados para Indice de Gini
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OBJETIVO: Analisar fatores determinantes do status de saúde em cada estado da Região Nordeste do Brasil. MÉTODOS: Estudo utilizando a metodologia de dados em painel, com informações agregadas para municípios. Os dados compreendem os anos de 1991 e 2000, e foram obtidos no Atlas do Desenvolvimento Humano do Programa das Nações Unidas para o Desenvolvimento, e Secretaria do Tesouro Nacional. Utilizou-se como indicador do status de saúde, a taxa de mortalidade infantil, e como determinantes as variáveis: gastos com saúde e saneamento per capita, números de médicos por mil habitantes, acesso à água tratada, taxa de fecundidade e de analfabetismo, percentual de mães adolescentes, renda per capita e índice de Gini. RESULTADOS: As taxas de mortalidade infantil na região Nordeste reduziram-se em 31,8% no período analisado, desempenho pouco superior ao apresentado para a média nacional. No entanto, em alguns estados, como Rio Grande do Norte, Bahia, Ceará e Alagoas, a redução foi mais significativa. Isso pode ser atribuído à melhora de alguns indicadores que são os principais determinantes da redução da taxa de mortalidade infantil: maior acesso à educação, redução da taxa de fecundidade, aumento da renda, e do acesso à água. CONCLUSÕES: Os estados que apresentaram maiores ganhos no acesso à água tratada, educação, renda e redução da taxa de fecundidade, foram também os que obtiveram maiores ganhos na redução da mortalidade de menores de um ano de idade.
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OBJETIVO: Analisar a influência dos fatores demográficos, socioeconômicos, de condições de saúde e do contexto das unidades da federação na incapacidade funcional dos idosos. MÉTODOS: Estudo transversal que utilizou dados da Pesquisa Nacional por Amostra de Domicílio (PNAD) de 2003, do Instituto Brasileiro de Geografia e Estatística (IBGE) e do Instituto de Pesquisa Econômica Aplicada (Ipea). A amostra foi constituída de 33.515 indivíduos com 60 anos ou mais de idade. A variável dependente foi a incapacidade funcional, mensurada pela dificuldade por subir ladeira ou escada. As variáveis independentes foram divididas em dois níveis: individual (características demográficas, socioeconômicas e relativas à saúde) e de contexto (Índice de Gini e Produto Interno Bruto per capita por unidade da federação em 2000). Um modelo de regressão logística multinomial multinível foi utilizado para estimar o efeito das variáveis independentes na incapacidade funcional dos idosos. RESULTADOS: A incapacidade funcional foi associada com fatores demográficos, socioeconômicos e de saúde. Em nível individual, o sexo, a educação, a renda, a ocupação, a autopercepção de saúde e as doenças crônicas foram os fatores mais fortemente relacionados. Em nível de contexto, a desigualdade de renda exibiu uma importante influência. CONCLUSÕES: A autopercepção de saúde é o fator mais fortemente relacionado com a incapacidade funcional dos idosos no Brasil, seguida das doenças crônicas. Sexo, ocupação, escolaridade e renda também são altamente associados. Ações que abordam os principais fatores associados à incapacidade funcional podem contribuir significativamente para o bem-estar e qualidade de vida dos idosos.
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OBJECTIVE: To analyze whether the relationship between income inequality and human health is mediated through social capital, and whether political regime determines differences in income inequality and social capital among countries. METHODS: Path analysis of cross sectional ecological data from 110 countries. Life expectancy at birth was the outcome variable, and income inequality (measured by the Gini coefficient), social capital (measured by the Corruption Perceptions Index or generalized trust), and political regime (measured by the Index of Freedom) were the predictor variables. Corruption Perceptions Index (an indirect indicator of social capital) was used to include more developing countries in the analysis. The correlation between Gini coefficient and predictor variables was calculated using Spearman's coefficients. The path analysis was designed to assess the effect of income inequality, social capital proxies and political regime on life expectancy. RESULTS: The path coefficients suggest that income inequality has a greater direct effect on life expectancy at birth than through social capital. Political regime acts on life expectancy at birth through income inequality. CONCLUSIONS: Income inequality and social capital have direct effects on life expectancy at birth. The "class/welfare regime model" can be useful for understanding social and health inequalities between countries, whereas the "income inequality hypothesis" which is only a partial approach is especially useful for analyzing differences within countries.
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OBJECTIVE: To analyze cause-specific mortality rates according to the relative income hypothesis. METHODS: All 96 administrative areas of the city of São Paulo, southeastern Brazil, were divided into two groups based on the Gini coefficient of income inequality: high (>0.25) and low (<0.25). The propensity score matching method was applied to control for confounders associated with socioeconomic differences among areas. RESULTS: The difference between high and low income inequality areas was statistically significant for homicide (8.57 per 10,000; 95%CI: 2.60;14.53); ischemic heart disease (5.47 per 10,000 [95%CI 0.76;10.17]); HIV/AIDS (3.58 per 10,000 [95%CI 0.58;6.57]); and respiratory diseases (3.56 per 10,000 [95%CI 0.18;6.94]). The ten most common causes of death accounted for 72.30% of the mortality difference. Infant mortality also had significantly higher age-adjusted rates in high inequality areas (2.80 per 10,000 [95%CI 0.86;4.74]), as well as among males (27.37 per 10,000 [95%CI 6.19;48.55]) and females (15.07 per 10,000 [95%CI 3.65;26.48]). CONCLUSIONS: The study results support the relative income hypothesis. After propensity score matching cause-specific mortality rates was higher in more unequal areas. Studies on income inequality in smaller areas should take proper accounting of heterogeneity of social and demographic characteristics.
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OBJETIVO: Estimar a prevalência e a distribuição geográfica da doença periodontal na população adulta brasileira e sua associação com desigualdades sociais contextuais e individuais. MÉTODOS: Foram utilizados dados dos adultos de 35 a 44 anos de idade da Pesquisa Nacional de Saúde Bucal – SBBrasil 2010 (n = 9.564). O Índice Periodontal Comunitário (CPI) e o Índice de Perda Periodontal (PIP) foram usados para definir a doença periodontal em “moderada a grave” (CPI > 2 e PIP > 0) e “grave” (CPI > 2 e PIP > 1). As desigualdades sociais contextuais incluíram o índice de desenvolvimento humano e a desigualdade de renda (Índice de Gini). Outras variáveis contextuais foram a cobertura de equipes de saúde bucal da Estratégia de Saúde da Família e o percentual de adultos fumantes. Modelos de regressão logística multinível para os participantes com dados completos (n = 4.594) foram usados para estimar odds ratios (OR) e intervalos de 95% de confiança (IC95%) entre desigualdades sociais e doença periodontal. RESULTADOS: A prevalência da doença periodontal “moderada a grave” em brasileiros adultos foi de 15,3% e 5,8% para a condição “grave”, com variações consideráveis entre os municípios. Dentre as variáveis contextuais, a desigualdade de renda foi independentemente associada com a doença periodontal “grave” (OR = 3,0; IC95% 1,5;5,9). A menor cobertura de equipes de saúde bucal foi associada com as duas formas de doença periodontal, enquanto o percentual de fumantes manteve-se associado com a doença periodontal “moderada a grave”. Adultos com idade mais avançada, de cor de pele parda, sexo masculino, menor renda familiar e menor escolaridade apresentaram maiores chances para ambas as condições periodontais investigadas. CONCLUSÕES: No Brasil, a prevalência da doença periodontal variou conforme o município e a definição de doença empregada. A desigualdade de renda teve um papel importante na ocorrência da doença periodontal “grave”. Características individuais de posição social foram associadas com as duas formas de doença periodontal.
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Introduction More than half of the malaria cases reported in the Americas are from the Brazilian Amazon region. While malaria is considered endemic in this region, its geographical distribution is extremely heterogeneous. Therefore, it is important to investigate the distribution of malaria and to determine regions whereby action might be necessary. Methods Changes in malaria indicators in all municipalities of the Brazilian Amazon between 2003-2004 and 2008-2009 were studied. The malaria indicators included the absolute number of malaria cases and deaths, the bi-annual parasite incidence (BPI), BPI ratios and differences, a Lorenz curve and Gini coefficients. Results During the study period, mortality from malaria remained low (0.02% deaths/case), the percent of municipalities that became malaria-free increased from 15.6% to 31.7%, and the Gini coefficient increased from 82% to 87%. In 2003, 10% of the municipalities with the highest BPI accumulated 67% of all malaria cases, compared with 2009, when 10% of the municipalities (with the highest BPI) had 80% of the malaria cases. Conclusions This study described an overall decrease in malaria transmission in the Brazilian Amazon region. As expected, an increased heterogeneity of malaria indicators was found, which reinforces the notion that a single strategy may not bring about uniformly good outcomes. The geographic clustering of municipalities identified as problem areas might help to define better intervention methods.
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Indices globais pulicidianos, anoplurianos, malofagianos e acarianos foram determinados em mamiferos capturados na Ilha de Manacá, Roraima, Brasil, no periodo de, novembro de 1987 a fevereiro de 1989.Tendo-se em vista os valores limites ou criticas atri-buidos aos indices pulicidianos, propostos como medida complementar de vigilância epide-miológica para peste, alguns, roedores silvestres poderiam ter estado expostos a esta in-fecção. O indice global foi de 11,5e a pulga prevalente foi Polygznis klagesi klagesiobservado na estação seca. Os números máximos de ectoparasitas por hospedeiros foram: 244 para Prorchimys guyannensis, 193para Prorchimyssp. e 108 para Bolomys sp. As espéciescom indices de infestação mais elevados fonam P. klagesi klagesiem Peoechimyssp.; Glíricolasp. n., Tur apicalise Tur aymaraem P. guyannensis.infestações simples foram de mais prevalentes, enquanto as duplas e as outras múltiplas foram equivalentes. Com exceção deProechimyssp., todas as espécies de hospedeiros apresentaram infestações simples. Apenas Laelaps dearmasie Gliricola porcelliocorreram em infestações iso-ladas.
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FUNDAMENTO: O acúmulo de gordura visceral é considerado o principal fator de risco para doenças cardiovasculares e metabólicas. OBJETIVO: Determinar a prevalência de obesidade visceral e avaliar sua associação com fatores de risco cardiovasculares em mulheres jovens do Estado de Pernambuco. MÉTODOS: Estudo transversal, realizado com dados da "III Pesquisa Estadual de Saúde e Nutrição", envolvendo mulheres entre 25 e 36 anos. Avaliaram-se as variáveis: Índice de Massa Corporal (IMC), Circunferência da Cintura (CC), Razão Cintura-Estatura (RCE), Volume de Gordura Visceral (VGV) estimado por equação preditiva, Pressão Arterial Sistólica e Diastólica (PAS, PAD), Colesterol Total (CT), Triglicerídeo (TG), Glicemia de Jejum (GJ). RESULTADOS: Foram avaliadas 517 mulheres, com mediana de idade de 29 anos (27-32) e prevalência de obesidade visceral de 30,6%. Valores de IMC, PAS, PAD e TG foram superiores no grupo com obesidade visceral: IMC = 28,0 kg/m² (25,0 - 21,4) vs 23,9 kg/m² (21,5 - 26,4); PAS = 120,0 mmHg (110,0 - 130,0) vs 112,0 mmHg (100,0 - 122,0); PAD = 74 mmHg (70 - 80) vs 70 mmHg (63 - 80); TG = 156,0 mg/dL (115,0 - 203,2) vs 131,0 mg/dL (104,0 - 161,0), respectivamente, p < 0,01. Idade, PAS, PAD, TG e CT apresentaram correlação positiva e significante com o VGV: r = 0,171; 0,224; 0,163; 0,278; 0,124; respectivamente, p < 0,005. CONCLUSÃO: Verificou-se uma elevada prevalência de obesidade visceral, estando estatisticamente correlacionada a fatores de risco cardiovasculares.
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FUNDAMENTO: Diversos autores correlacionaram o aumento do risco cardiovascular com o estado nutricional, porém existem diferentes critérios para a classificação de sobrepeso e obesidade em crianças. Objetivos: Avaliar o desempenho de três critérios de classificação nutricional em crianças, como definidores da presença de obesidade e preditores de níveis pressóricos elevados em escolares. MÉTODOS: Oitocentas e dezessete crianças de 6 a 13 anos matriculadas em escolas públicas do município de Vila Velha (ES) foram submetidas a avaliação antropométrica e de pressão arterial. A classificação quanto ao estado nutricional foi estabelecida mediante dois critérios internacionais (CDC/NCHS 2000 e IOTF 2000) e um critério brasileiro (Conde e Monteiro 2006). RESULTADOS: A prevalência de excesso de peso foi maior quando utilizado o critério de Conde e Monteiro (27%), e menor pelo critério do IOTF (15%). Pressão arterial elevada foi observada em 7,3% das crianças. Identificou-se forte associação entre a presença de excesso de peso e a ocorrência de níveis pressóricos elevados, independentemente do critério utilizado (p < 0,001). O critério que demonstrou maior sensibilidade em prever PA elevada foi o de Conde e Monteiro (44%), enquanto o de maior especificidade (94%), além de maior acurácia geral (63%), foi o do CDC. CONCLUSÕES: A prevalência de excesso de peso em crianças brasileiras é maior quando utilizado o critério de classificação de Conde e Monteiro, e menor quando utilizado o critério do IOTF. O critério de classificação brasileiro demonstrou ser o mais sensível como preditor de risco de PA elevada nessa amostra.
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Size and shape in eggs of Rhode Island Red and Light Sussex breeds and in the hibrid Rhode x Sussex were studied. These characters are influenced by quantitative genes. Major and minor diameter were used for estimating size of the eggs and the ratio minor/major diameter for shape indice. It was found, in the material analyzed, that: a) the eggs laid by the sa- me chick are pratically uniform; b) the correlation coeficient between major and minor diameter is weak; c) Rhode Island Red has short eggs than Light Sussex; d) short eggs is dominant on long eggs; e) egg shape is the same in Rhode Island Red and Light Sussex breeds and different in the hibrid, which has rounder eggs than the breeds.
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This paper deals with problems on population genetics in Hymenoptera and particularly in social Apidae. 1) The studies on populations of Hymenoptera were made according to the two basic types of reproduction: endogamy and panmixia. The populations of social Apinae have a mixed method of reproduction with higher percentage of panmixia and a lower of endogamy. This is shown by the following a) males can enter any hive in swarming time; b) males of Meliponini are expelled from hives which does not need them, and thus, are forced to look for some other place; c) Meliponini males were seen powdering themselves with pollen, thus becoming more acceptable in any other hive. The panmixia is not complete owing to the fact that the density of the breeding population as very low, even in the more frequent species as low as about 2 females and 160 males per reproductive area. We adopted as selection values (or survival indices) the expressions according to Brieger (1948,1950) which may be summarised as follows; a population: p2AA + ²pq Aa + q2aa became after selection: x p2AA + 2pq Aa + z q²aa. For alge-braics facilities Brieger divided the three selective values by y giving thus: x/y p2 AA + y/y 2 pq Aa + z/y q²aa. He called x/y of RA and z/y of Ra, that are survival or selective index, calculated in relation to the heterozygote. In our case all index were calculated in relation to the heterozygote, including the ones for haploid males; thus we have: RA surveval index of genotype AA Ra surveval index of genotype aa R'A surveval index of genotype A R'a surveval index of genotype a 1 surveval index of genotype Aa The index R'A ande R'a were equalized to RA and Ra, respectively, for facilities in the conclusions. 2) Panmitic populations of Hymenoptera, barring mutations, migrations and selection, should follow the Hardy-Weinberg law, thus all gens will be present in the population in the inicial frequency (see Graphifc 1). 3) Heterotic genes: If mutation for heterotic gene ( 1 > RA > Ra) occurs, an equilibrium will be reached in a population when: P = R A + Ra - 2R²a _____________ (9) 2(R A + Ra - R²A - R²a q = R A + Ra - 2R²A _____________ (10) 2(R A + Ra - R²A - R²a A heterotic gene in an hymenopteran population may be maintained without the aid of new mutation only if the survival index of the most viable mutant (RA) does not exced the limiting value given by the formula: R A = 1 + √1+Ra _________ 4 If RA has a value higher thah the one permitted by the formula, then only the more viable gene will remain present in the population (see Graphic 10). The only direct proof for heterotic genes in Hymenoptera was given by Mackensen and Roberts, who obtained offspring from Apis mellefera L. queens fertilized by their own sons. Such inbreeding resulted in a rapid loss of vigor the colony; inbred lines intercrossed gave a high hybrid vigor. Other fats correlated with the "heterosis" problem are; a) In a colony M. quadrifasciata Lep., which suffered severely from heat, the percentage of deths omong males was greater .than among females; b) Casteel and Phillips had shown that in their samples (Apis melifera L). the males had 7 times more abnormalities tian the workers (see Quadros IV to VIII); c) just after emerging the males have great variation, but the older ones show a variation equal to that of workers; d) The tongue lenght of males of Apis mellifera L., of Bombus rubicundus Smith (Quadro X), of Melipona marginata Lep. (Quadro XI), and of Melipona quadrifasciata Lep. Quadro IX, show greater variationthan that of workers of the respective species. If such variation were only caused by subviables genes a rapid increasse of homozigoty for the most viable alleles should be expected; then, these .wild populations, supposed to be in equilibrium, could .not show such variability among males. Thus we conclude that heterotic genes have a grat importance in these cases. 4) By means of mathematical models, we came to the conclusion tht isolating genes (Ra ^ Ra > 1), even in the case of mutations with more adaptability, have only the opor-tunity of survival when the population number is very low (thus the frequency of the gene in the breeding population will be large just after its appearence). A pair of such alleles can only remain present in a population when in border regions of two races or subspecies. For more details see Graphics 5 to 8. 5) Sex-limited genes affecting only females, are of great importance toHymenoptera, being subject to the same limits and formulas as diploid panmitic populations (see formulas 12 and 13). The following examples of these genes were given: a) caste-determining genes in the genus Melipona; b) genes permiting an easy response of females to differences in feeding in almost all social Hymenoptera; c) two genes, found in wild populations, one in Trigona (Plebéia) mosquito F. SMITH (quadro XII) and other in Melipona marginata marginata LEP. (Quadro XIII, colonies 76 and 56) showing sex-limited effects. Sex-limited genes affecting only males do not contribute to the plasticity or genie reserve in hymenopteran populations (see formula 14). 6) The factor time (life span) in Hymenoptera has a particular importance for heterotic genes. Supposing one year to be the time unit and a pair of heterotic genes with respective survival indice equal to RA = 0, 90 and Ra = 0,70 to be present; then if the life time of a population is either one or two years, only the more viable gene will remain present (see formula 11). If the species has a life time of three years, then both alleles will be maintained. Thus we conclude that in specis with long lif-time, the heterotic genes have more importance, and should be found more easily. 7) The colonies of social Hymenoptera behave as units in competition, thus in the studies of populations one must determine the survival index, of these units which may be subdivided in indice for egg-laying, for adaptive value of the queen, for working capacity of workers, etc. 8) A study of endogamic hymenopteran populations, reproduced by sister x brother mating (fig. 2), lead us to the following conclusions: a) without selection, a population, heterozygous for one pair of alleles, will consist after some generations (theoretically after an infinite number of generation) of females AA fecundated with males A and females aa fecundated with males a (see Quadro I). b) Even in endogamic population there is the theoretical possibility of the presence of heterotic genes, at equilibrium without the aid of new mutations (see Graphics 11 and 12), but the following! conditions must be satisfied: I - surveval index of both homozygotes (RA e Ra) should be below 0,75 (see Graphic 13); II - The most viable allele must riot exced the less viable one by more than is permited by the following formula (Pimentel Gomes 1950) (see Gra-fic 14) : 4 R5A + 8 Ra R4A - 4 Ra R³A (Ra - 1) R²A - - R²a (4 R²a + 4 Ra - 1) R A + 2 R³a < o Considering these two conditions, the existance of heterotic genes in endogamic populations of Hymenoptera \>ecames very improbable though not - impossible. 9) Genie mutation offects more hymenopteran than diploid populations. Thus we have for lethal genes in diploid populations: u = q2, and in Hymenoptera: u = s, being u the mutation ratio and s the frequency of the mutant in the male population. 10) Three factors, important to competition among species of Meliponini were analysed: flying capacity of workers, food gathering capacity of workers, egg-laying of the queen. In this connection we refer to the variability of the tongue lenght observed in colonies from several localites, to the method of transporting the pollen in the stomach, from some pots (Melliponi-ni storage alveolus) to others (e. g. in cases of pillage), and to the observation that the species with the most populous hives are almost always the most frequent ones also. 11) Several defensive ways used for Meliponini to avoid predation are cited, but special references are made upon the camouflage of both hive (fig. 5) and hive entrance (fig. 4) and on the mimetism (see list in page ). Also under the same heading we described the method of Lestrimelitta for pillage. 12) As mechanisms important for promoting genetic plasticity of hymenopteran species we cited: a) cytological variations and b) genie reserve. As to the former, duplications and numerical variations of chromosomes were studied. Diprion simile ATC was cited as example for polyploidy. Apis mellife-ra L. (n = 16) also sugests polyploid origen since: a) The genus Melipona, which belongs to a" related tribe, presents in all species so far studied n = 9 chromosomes and b) there occurs formation of dyads in the firt spermatocyte division. It is su-gested that the origin of the sex-chromosome of Apis mellifera It. may be related to the possible origin of diplo-tetraploidy in this species. With regards to the genie reserve, several possible types of mutants were discussed. They were classified according to their survival indices; the heterotic and neutral mutants must be considered as more important for the genie reserve. 13) The mean radius from a mother to a daghter colony was estimated as 100 meters. Since the Meliponini hives swarm only once a year we may take 100 meters a year as the average dispersion of female Meliponini in ocordance to data obtained from Trigona (tetragonisca) jaty F. SMITH and Melipona marginata LEP., while other species may give different values. For males the flying distance was roughly estimated to be 10 times that for females. A review of the bibliography on Meliponini swarm was made (pg. 43 to 47) and new facts added. The population desity (breeding population) corresponds in may species of Meliponini to one male and one female per 10.000 square meters. Apparently the males are more frequent than the females, because there are sometimes many thousands, of males in a swarm; but for the genie frequency the individuals which have descendants are the ones computed. In the case of Apini and Meliponini, only one queen per hive and the males represented by. the spermatozoos in its spermateca are computed. In Meliponini only one male mate with the queen, while queens of Apis mellijera L. are fecundated by an average of about 1, 5 males. (Roberts, 1944). From the date cited, one clearly sees that, on the whole, populations of wild social bees (Meliponini) are so small that the Sewall Wright effect may become of great importance. In fact applying the Wright's formula: f = ( 1/aN♂ + 1/aN♀) (1 - 1/aN♂ + 1/aN♀) which measures the fixation and loss of genes per generation, we see that the fixation or loss of genes is of about 7% in the more frequent species, and rarer species about 11%. The variation in size, tergite color, background color, etc, of Melipona marginata Lep. is atributed to this genetic drift. A detail, important to the survival of Meliponini species, is the Constance of their breeding population. This Constance is due to the social organization, i. e., to the care given to the reproductive individuals (the queen with its sperm pack), to the way of swarming, to the food storage intended to control variations of feeding supply, etc. 14) Some species of the Meliponini are adapted to various ecological conditions and inhabit large geographical areas (e. g. T. (Tetragonisca jaty F. SMITH), and Trigona (Nanno-trigona testaceicornis LEP.) while others are limited to narrow regions with special ecological conditions (e. g. M. fuscata me-lanoventer SCHWARZ). Other species still, within the same geographical region, profit different ecological conditions, as do M. marginata LEP. and M. quadrifasciata LEP. The geographical distribution of Melipona quadrifasciata LEP. is different according to the subspecies: a) subsp anthidio-des LEP. (represented in Fig. 7 by black squares) inhabits a region fron the North of the S. Paulo State to Northeastern Brazil, ,b) subspecies quadrifasciata LEP., (marked in Fig. 7 with black triangles) accurs from the South of S. Paulo State to the middle of the State of Rio Grande do Sul (South Brazil). In the margined region between these two areas of distribution, hi-brid colonies were found (Fig. 7, white circles); they are shown with more details in fig. 8, while the zone of hybridization is roughly indicated in fig. 9 (gray zone). The subspecies quadrifasciata LEP., has 4 complete yellow bands on the abdominal tergites while anthidioides LEP. has interrupted ones. This character is determined by one or two genes and gives different adaptative properties to the subspecies. Figs. 10 shows certains meteorological isoclines which have aproximately the same configuration as the limits of the hybrid zone, suggesting different climatic adaptabilities for both genotypes. The exis-tance of a border zone between the areas of both subspecies, where were found a high frequency of hybrids, is explained as follows: being each subspecies adapted to a special climatic zone, we may suppose a poor adaptation of either one in the border region, which is also a region of intermediate climatic conditions. Thus, the hybrids, having a combination of the parent qualities, will be best adapted to the transition zone. Thus, the hybrids will become heterotic and an equilibrium will be reached with all genotypes present in the population in the border region.
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Uma amostra de T. cruzi foi isolada pela primeira vez de um exemplar do Triatoma costalimai, capturado no município de Mambai, Goiás. Estudos experimentais sobre infectividade e virulência foram conduzidos em triatomíneos, Calomys callosus (Rodentia) e camundongos albinos. Cultivo "In Vitro" da amostra isolada foi obtido com sucesso utilizando-se o meio LIT. As mensurações realizadas em tripomastigotas sanguícolas deram os seguintes resultados (mcg): comprimento total - 16,4 (± 1,1); flagelo livre - 4,9 (± 1,1); largura - 2,8 (± 0,6); distância NA - 4,8 (± 0,6); distância NP - 6,0 (± 0,5) e Indice nuclear 1,3.
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Oitenta e uma macaubeiras (A. sclerocarpa) foram derrubadas e dissecadas na periferia de Belo Horizonte, no período de abril/ 1979 a julho/1980. Foram capturados 463 exemplares de Rhodnius neglectus, com uma taxa de infestação das palmeiras de 60,5% e uma média de 9,45% triatomineos/palmeira positiva. O R. neglectus nesta região parece apresentar uma unica geração anual, com possibilidade de duas, sendo que o periodo de oviposição se relaciona com os meses quentes do ano, coincidindo com a predominância de formas jovens sobre os adultos. A observação sugere que a densidade populacional do R. neglectus no seu ecotopo natural possa estar relacionada com a disponibilidade de alimento e com a presença de predadores como o Telenomus sp., formigas, aranhas, hemipteros, escorpiões e pseudo-escorpiões. O indice global de infecção pelo Trypanosoma cruzi foi de 15,9%, indicando o R. neglectus como um importante vetor silvestre deste tripanosomatídeo cuja principal fonte e constituída por marsupiais. O R. neglectus na regiao encontra-se estreitamente associado a palmeira de macaúba, e as aves que as frequentam constituem sua principal fonte alimentar. As observações não sugerem o R.neglectus como uma espécie transmissora do T. cruzi ao homem nesta região.
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Schistosoma intercalatum, which causes human rectal schistosomiasis in Africa, still presents a great interest for its imprecise taxonomic status and its puzzling distribution in Africa. Two geographically isolated strains of S. intercalatum are recognized, the Lower Guinea strain and the Congo strain, which differ from each other in a number of morphological, biological and biochemical characteristics. Recent molecular data using RAPD markers indicate high divergence between the two strains, with values of Nei and Li's similarity indice allowing recognition of two genetically distinct taxa: experiments on pre- and post-isolating mechanisms are in progress in order to re-evaluate the taxonomic status of this polytypic species. With regard to its geographical distribution, S. intercalatum is characterized by the existence of two stable endemic areas (localized in Lower Guinea and North East of Democratic Republic of Congo) which correspond to the historical areas of species discovery, and the emergence during the last 15 years of new foci of the Lower Guinea strain outside previously known endemic areas. The absence of local adaptation of the Lower Guinea strain to its intermediate host, supported by experimental studies, may help to facilitate the spread of this strain. Nevertheless, the present restricted distribution of this species remains puzzling, because its potential snail hosts (bulinids) are widely distributed throughout much of Africa. Recent experimental and epidemiological studies suggest that interspecific sexual interactions between human schistosomes could have a role in limiting the distribution of S. intercalatum: the competitive sexual processes acting among human schistosomes show that S. haematobium and S. mansoni are always competitively dominant over S. intercalatum. These epidemiological observations lead the authors to distinguish three kinds of transmission foci for S. intercalatum.
Resumo:
The objective of this work was to evaluate sampling density on the prediction accuracy of soil orders, with high spatial resolution, in a viticultural zone of Serra Gaúcha, Southern Brazil. A digital elevation model (DEM), a cartographic base, a conventional soil map, and the Idrisi software were used. Seven predictor variables were calculated and read along with soil classes in randomly distributed points, with sampling densities of 0.5, 1, 1.5, 2, and 4 points per hectare. Data were used to train a decision tree (Gini) and three artificial neural networks: adaptive resonance theory, fuzzy ARTMap; self‑organizing map, SOM; and multi‑layer perceptron, MLP. Estimated maps were compared with the conventional soil map to calculate omission and commission errors, overall accuracy, and quantity and allocation disagreement. The decision tree was less sensitive to sampling density and had the highest accuracy and consistence. The SOM was the less sensitive and most consistent network. The MLP had a critical minimum and showed high inconsistency, whereas fuzzy ARTMap was more sensitive and less accurate. Results indicate that sampling densities used in conventional soil surveys can serve as a reference to predict soil orders in Serra Gaúcha.