Podridão-mole em plantas de cebolinha causada por Pectobacterium carotovorumsubsp. carotovorum em Roraima

A ocorrência de Pectobacterium carotovorum subsp. carotovorum (=Erwinia carotovora subsp. carotovora) em cebolinha (Allium fistulosum) é relatada pela primeira vez na região norte do Brasil. Até então sua ocorrência estava registrada apenas no Distrito Federal.

Efeito da exploração madeireira sobre o número de indivíduos férteis de três espécies arbóreas comerciais na Amazônia oriental

Estudos da ecologia reprodutiva de árvores são fundamentais para compreender os possíveis impactos da exploração madeireira e para subsidiar o aperfeiçoamento das práticas de manejo. Os objetivos desse trabalho foram: 1) estimar a proporção e o número de indivíduos reprodutivos por classe de diâmetro de Chrysophyllum lucentifolium subsp. pachycarpum, Lecythis lurida e Pseudopiptadenia psilostachya, três espécies madeireiras, em uma floresta em Paragominas (PA) e; 2) estimar o impacto da exploração de 90% dos indivíduos com DAP > 50 cm sobre o número de indivíduos reprodutivos das mesmas espécies no local. Durante uma estação reprodutiva de cada espécie, foram amostradas 80 árvores de L. lurida, 76 de P. psilostachya e 76 de C. lucentifolium. Foi estimado que 14,9% de todos os indivíduos férteis de C. lucentifolium, 35,9% de L. lurida e 72,4% de P. psilostachya tinham DAP > 50 cm no ano de amostragem. Assim, o corte de 90% dessas árvores causaria uma redução de 13,4%, 32,6 % e 65,2 % do número de indivíduos férteis de C. lucentifolium, L. lurida e P. psilostachya, respectivamente. Se as proporções de indivíduos férteis fossem constantes ao longo do tempo, para preservar metade dos indivíduos férteis de P. psilostachya seria necessário manter 30% e não 10% daqueles com DAP > 50 cm. Os resultados indicam que, adotando-se um único diâmetro mínimo de corte e retendo-se a mesma proporção de árvores acima desse diâmetro, o efeito em termos de porcentagem de indivíduos reprodutivos retirados da população pode variar entre espécies na ordem de aproximadamente cinco vezes.

Mimosoideae (Leguminosae) do litoral paraense

Este trabalho consiste no tratamento taxonômico de Mimosoideae nas restingas do litoral paraense, uma vez que estas são pouco conhecidas sob esse aspecto. Esse estudo abrangeu a análise do material proveniente de coletas e exsicatas dos herbários MG e IAN, além de literatura especializada. São apresentadas chave de identificação, descrições e ilustrações dos táxons, bem como dados adicionais sobre distribuição geográfica, comentários, período de floração e frutificação e hábitat das mesmas. O fruto foi o caráter de maior destaque na separação dos táxons. Os resultados evidenciaram a presença de sete espécies, três variedades e uma subespécie, distribuídas em seis gêneros. Inga thibaudiana subsp. thibaudiana e Mimosa candollei, são novos registros para o litoral do Pará. O gênero Inga Mill. foi o mais representativo com cinco espécies. Entada polystachya var. polystachya e principalmente Chloroleucon acacioides apresentaram distribuição mais ampla e a formação floresta de restinga foi o ecossistema que apresentou o maior número de espécie.

Chemical composition of the essential oils from two subspecies of Protium heptaphyllum

Qualitative and quantitative analyses of the volatile constituents from resin of Protium heptaphyllum (Aubl.) Marchand subsp. ulei (Swat) Daly (PHU), and Protium heptaphyllum (Aubl.) Marchand subsp. heptaphyllum (PHH), Burseraceae were performed using GC-MS and GC-FID. The resins were collected around the city of Cruzeiro do Sul, state of Acre, Brazil. Essential oils from the two subspecies were extracted by hydrodistillation with a yield of 8.6% (PHU) and 11.3% (PHH); the main components were terpinolene (42.31%) and p-cymene (39.93%) for subspecies ulei (PHU) and heptaphyllum (PHH), respectively.

Avaliação das propriedades de painéis aglomerados produzidos com resíduos de serrarias de nove espécies de madeiras tropicais da Amazônia

Esta pesquisa teve como objetivo avaliar a qualidade de painéis aglomerados produzidos com resíduos de processamento em serraria de nove espécies de madeiras tropicais da Amazônia. As espécies estudadas foram: Scleronema micranthum Ducke (Cardeiro), Ecclinusa guianensis Eyma (Caucho), Scleronema sp. (Castanha-de-paca), Copaifera multijuga Hayne (Copaíba), Ocotea sp. (Louro), Ocotea guianensis Aubl (Louro-espinho), Caryocar villosum Pers. (Piquiarana), Couratari oblongifolia Ducke & R. Knuth (Tauari) e Virola surinamensis Rol. Warb (Virola). Foram produzidos painéis experimentais com densidade nominal de 0,75 g.cm-3, utilizando a resina uréia-formaldeído na proporção de 8% de sólidos - base peso seco das partículas. Os painéis foram prensados com pressão específica de 4,0 MPa, temperatura de 160 ºC e tempo de prensagem de oito minutos. As avaliações dos resultados de ensaios obtidos nesta pesquisa indicam a viabilidade técnica de utilização das nove espécies provenientes de florestas tropicais da Amazônia na produção de painéis de madeira aglomerada, com destaque para Ecclinusa guianensis Eyma (Caucho) que, de uma forma geral, apresentou melhores resultados de propriedades físico-mecânicas.

Fitossociologia e uso múltiplo de espécies arbóreas em floresta manejada, comunidade Santo Antônio, município de Santarém, estado do Pará

Avaliou-se a fitossociologia de floresta manejada em lotes de comunitários da Comunidade Santo Antônio no Assentamento Moju I e II, município de Santarém, Amazônia brasileira. Foram instaladas 12 parcelas de 50 m x 200 m (1 por lote) anotando-se indivíduos com CAP ≥ 157,1 cm (nível 3 de inclusão); 12 sub-parcelas de 50 m x 50 m, para os indivíduos com 94,2 cm ≤ CAP < 157,1 cm (nível 2 de inclusão) e 12 sub-parcelas de 50 m x 25 m, para os indivíduos com 31,4cm ≤ CAP < 94,2 cm (nível 1 de inclusão). Foram amostrados 1.227 indivíduos, distribuídos em 175 espécies e 38 famílias botânicas. A família Fabaceae apresentou maior número de espécies e o gênero mais rico foi Inga. O Índice de Diversidade de Shannon (H') foi 4,39 e o Índice de Equabilidade de Pielou (J) de 0,85. A avaliação do Valor de Importância Ampliado (VIA) das espécies da amostra revelou o estoque de espécies com potencial madeireiro e não madeireiro. Carapa guianensis, Caryocar villosum, Brosimum parinarioides, Aniba canellila, Bowdichia virgilioides e Andira surinamensis podem ser aproveitadas como produtos florestais não madeireiros e serem removidas da lista de espécies de corte para fins madeireiros, melhorando assim o retorno econômico comunitário. Manilkara huberi e Carapa guianensis foram espécies com utilização madeireira e não madeireira mais expressivas, considerando o mercado atual e potencial de usos conhecidos; portanto, tais características devem ser consideradas no planejamento e execução do manejo da floresta.

Estudo taxonômico de Sapotaceae Juss. do litoral Paraense

Este trabalho consiste no tratamento taxonômico de Sapotaceae Juss. nas restingas do litoral paraense. Com auxilio de estereomicroscópio foram feitas as descrições morfológicas das partes vegetativas e reprodutivas. Utilizou-se literatura especializada, coleções identificadas por especialistas para confirmar as características diferenciais dos táxons e montada uma chave de identificação para as espécies. Foram descritas cinco espécies e quatro subespécies, distribuídas em quatro gêneros: Manilkara bidentata subsp. bidentata, M. bidentata subsp. surinamensis, M. triflora, M. paraensis; Micropholisvenulosa, M. gnaphaloclados; Pouteria ramiflora, P. reticulata subsp. reticulata and Pradosia schomburgkiana subsp. schomburgkiana. O gênero Manilkara Adans.foi o mais representativo com duas espécies e duas subespécies. A formação floresta de restinga foi o ecossistema que apresentou o maior número de táxons.

Anatomical and energy characteristics of charcoal made from five species

Charcoal is an important energy raw material and its properties are influenced by the wood's anatomical and chemical composition and the production process. The aim of this study was to evaluate the anatomical characteristics, calorific power and volatiles and ash content of carbonized wood from Byrsonima spicata, Calophyllum brasiliense, Cecropia sciadophylla, Cochlospermum orinocense and Schefflera morototoni. The calorific power varied from 26,878 to 31,117 kJ kg-1; the content of volatile materials ranged from 20.9 to 31.7%; ash content ranged from 0.1 to 3.8%; and carbon content varied from 68.2 to 75.3%. Anatomical structures of charcoal can be used for species identification. The studied species are not indicated for charcoal production because the levels of ash and volatile compounds are higher than those recommended for charcoal produced for household use. In addition, the calorific power and level of carbon content are insufficient for use in the steel industry.

Bases para o estudo da genética de populações dos Hymenoptera em geral e dos Apinae sociais em particular

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.

Ixodidas brasileiros e de alguns paizes limitrophes

The knowledge of the Ixodidae becomes every day, more and more important owing to the fact of the increasing number of diseases of man and animals they can transmit. In Brasil besides transmitting treponemosis, piroplasmosis and anaplasmosis to several domestic animals, the ticks are also responsible fo the transmission of the brazilian rocky mountain spotted fever (A. cajennense and Amblyomma striatum) and they can also harbour the virus of the yellow fever and even to transmit it in laboratory experiments (A. cajennense, O. rostratus). The Brazilian fauna of ticks is a small one and has no more than 45 well-established species belonging to the genus Argas, Ornithodoros, Ixodes, Haemaphysalis, Rhipicephalus, Boophilus, Amblyomma and Spaelaeorhynchus. The genus Amblyomma is the best represented one, with 67% of all species of ticks known in Brazil. One of the most important species in the Amblyomma cajennense owing to its abundance and its wide parasitism in many vertebrates: reptiles, birds and mammals, incluing man, who is much attacked by the larva, the nymph and the adult of this species. The other ticks who attack the man are the Amblyomma brasiliense (the pecari tick), in the forests, and the Ornithodoros, especially the species. O. rostratus and brasiliensis. Other species can bite the man, but only occasionally, like Amblyomma fossum, striatum, oblongogutatum etc. Argas persicus, Rhipicephalus sanguineus and Boophilus are very important species not only as parasites but specially because they transmit several diseases to animals. Some of the ticks of the brazilian wild animals are now also parasites of the domestic ones and vice-versa. Arga persicus var. dissimilis is very common among the poultry and transmits the Treponema anserinum (gallinarum). Boophilus microplus is very abundant on our domestic and wild ruminants (Bos, Cervus, Mazama etc.) and can also ben found on horse, dogs, Felis onca, Felis concolor etc., and it transmits to cattle piroplasmosis and anaplasmosis. Rhipicephalus sanguineus (an introduced species) is now very common on the dog, over all the country. The author recommend to give popular names to some brazilian ticks in order to make them more acquainted with the non scientific people. The author gives a classification of the superfamilia Ixoidoidea and keys to the determination of the different species of brazilian ticks. He creates a new family of Nuttallielidae to the so interesting tick, described by Bedford with the name of Nuttaliella namaqua in South Africa, a new variety of Argas persicus, the Argas persicus var. dissimilis nov. var. owing to the differences on the segment and on the size and morphology of the peritrema. He describes also the female of Amblyomma fuscum Nn. A great part of the author's work deals with the biology, life conditions and parasitism of many of the brazilian ticks in accordance with his personal and from other author's researches, especially in reference to Argas persicus, Ornithodoros rostratus, O. brasiliensis, Boophilus microplus, Rhipicephalus sanguineus, Amblyomma cajennense, A. pseudoconcolor, A. auriculare, A. rotundatum (= A. agamum) etc. The author gives a detailed report upon the parthenogenesis of A. rotundatum (A. agamum) that he first described in 1912 and gives also many references to other species of brazilian ticks, to teratological forms etc. He also gives a detailed report of the geographical distribution of brazilian ticks and of the peculiar conditions of its parasitism. The last part of this article deals with references to the species of ticks of some of the South American Republics namely Argentina, Bolivia, Colombia, Paraguay and Venezuela. Amblyomma testudinis Conil, A. neumanni Ribaga 1902 (= A. furcula Dõnitz 1909) and A. parvitarsum Nn. 1899 (= A. altiplanum Dios 1917), are found only in Argentina. It is given a special bibliography dealing with the brazilian ticks and four text figures and one plate.

Profilaxia do tifo exantemático neotrópico no Brasil

A profilaxia racional de um doença decorre do melhor e mais profundo conhecimento dela. A do tifo exantematico neotrópico, apesar do que se sabe da doença, não e fácil no Brasil. Uma das maiores dificuldade encontramos nas distancias do nosso "hinterland" e na falta de cultura dos nossos agricultores. O homem se infecta certamente com as raças VB, VA e VA do virus brasileiro: 1.°) no campo, nas matas e nas macegas; 2.°) dentro dos domicílios ou nos arredores dêstes. Os primeiros constitúem de regra, os casos insulados do mal. Os segundos fazem parte, não raro, dos focos domiciliares macicos, com 2, 5, 7 e até 12 casos na mesma casa. São responsáveis, pelos primeiros, os carrapatos, principalmente o Amblyomma cayennense e o Amblyomma brasiliense, mormente quando no estado de ninfas, dada a herança habitual das infecções nesses artrópodos, que se infestam em animais silvestres, depositários do virus. São responsáveis pelos segundos, os "Cimex lectularius", percevejos dos leitos e as ninfas e larvas dos carrapatos, deixadas cair junto aos domicílios ou mesmo dentro deles. A profilaxia racional e completa da doença entre nós compreende: 1.°) Descarrapatização das zonas infestadas, por meio de leis apropriadas, coercitivas e aplicadas sem excepção; 2.°) Combate aos cães vadios, cabritos e outros animais portadores do virus; 3.°) Queima dos pastes, campos e macegas de fraco valor econômico, principalmente os que confinam com residências; 4.°) A propaganda racional contra esta grave doença exantemática: a) com palestras locais, acompanhadas de fotografias e gráficos expressivos e ao alcance de todos; b) pelo cinema; c) com artigos simples, claros e precisos sôbre a matéria; d) com folhetos apropriados; 5.°) Combater toda a vermina dentro e nas proximidades dos domicílios, 6.°) Demonstrar que é possível, com toda a certeza, evitar a doença, retirando os carrapatos que se prenderem ao corpo, dentro de 12 ou 14 horas após a fixação; 7.°) Aconselhar o emprego do DDT, “Gammexame" e “Toxafeno" para o expurgo das casas e animais, a fim de combater os carrapatos; 8.°) Vacinação preventiva contra a doença, quando possível, em zonas delimitadas e já civilizadas, feitas principalmente com raças de virus colhidas no Brasil e, se possível, com uma só dose. O autor trabalhou durante algum tempo com a vacina tipo Spencer-Parker. Hoje aconselha o trabalho com a vacina tipo Cox, original ou modificada.

Notas de Ixodologia: IV - considerações sôbre a nomeclatura de algumas espécies do gênero Amblyomma do Brasil e países limítrofes (Acari: Ixodidae)

An attempt is made to clear the nomenclature of some netropical species of the genus Amblyomma. Amblyomma myrmecophagium Schulze, 1933 and Amblyomma brasiliense guyanense Floch et Abonnenc, 1933, are synonyms of Amblyoma scalpturatum Neumann, 1906. Amblyomma superbrasiliense Schulze, 1941, is cospecific with Amblyomma incisum Neumann, 1906. Amblyomma ypsilophorum Schulze, 1941, is a synonym of Amblyomma cooperi Nuttal et Warburton, 1907.

Notas de ixodologia: V - A propósito da validade de algumas espécies do gênero Amblyomma do continente americano (Acari: Ixodídoe)

a) The species Amblyomma tapiri Tonelli Rondelli, 1937 and Amblyomma finitimum Tonelli Rondelli, 1937 are synonymous with Amblyomma cajennense Fabricius, 1787. Both species are based in differences of size, colour, punctations and form of the dorsal shield, presence or absence of ventral plates, size, form and direction of the spine of coxa IV. Such differences prouved to be only variations frequently observed in large lots or in cultures of Amblyomma cajennense. The revalidation of Koch's species Amblyomma tenellum Koch, 1844 and Amblyomma mixtum Koch, 1844 proposed by TONELLI RONDELLI as also of Amblyomma sculptum Berlese, 1888 and Amblyomma versicolor Nuttal et Warburton, 1908 cannot be accepted by the same reasons. b) Amblyomma beccari Tonelli Rondelli, 1939 and Amblyomma latepunctatum Tonelli Rondelli, 1939 are cospecific with Amblyomma scalpturatum Neumann, 1899 the same being true for Amblyomma myrmecophagium Schulze, 1935 and for Amblyomma brasiliense var. guianense Floch et Abonnenc, 1940, as previously stated. c) Amblyomma tasquei Floch et Abonnenc, 1940 is a good species but synonym with Amblyomma romitii Tonelli Rondelli, 1939 which has priority. d) Amblyomma curruca Schulze, 1936 is a synonym of Amblyomma parvum Aragão, 1908. e) Amblyomma deminutivum Neumann, 1899 represents a variation of Amblyomma dissimile Koch, 1844, a species whose internal spine of coxa IV may be poorly developed or even absent. f) Amblyomma nigrum Tonelli Rondelli, 1939 prouved to be synonym with Amblyomma paccae Aragao, 1911 the type representing a blackish specimen of the later species. g) Amblyomma brimonti Neumann, 1913 is a synonym of Amblyomma humerale Koch, 1844.

Saccocoelioides godoyi n.sp. (Haploporidae) and other trematodes parasites of fishes from the Guaiba estuary, RS, Brazil

One hundred and fourteen specimens of eleven different species of freshwater fishes from the Guaiba estuary, were examined for digenetic flukes. Saccocoelioides godoyi n.sp. proposed herein, is closest to S. magniovatus and to S. szidati; S. magniovatus is much smaller with comparably larger eggs and S. szidati has larger hermaphroditic sac and considerably larger testis. Creptotrema creptotrema is referred to a new host; Acanthostomum gnerii, Crepidostomum platense, Eocreadium intermedium (immature form), Parspina argentinensis and Zonocotyle bicaecata are reported. This paper confirms the similatary between the parasites of freshwater fishes from Argentina and Brazil. Measurements and original figures of all species are given.

Distribution of Sandflies (Diptera:Psychodidae) on Tree-trunks in a Non-flooded Area of the Ducke Forest Reserve, Manaus, AM, Brazil

Sandflies were collected in the base of tree-trunks in the seasons of high and least rainfall in the Ducke Forest Reserve, near Manaus in the State of Amazonas. Lutzomyia umbratilis was the most abundant sandfly species. Caryocar villosum, Chrysophyllum amazonicum, Dinizia excelsa, Eschweilera atropetiolata and Parkia multijuga were the tree species on which most sandflies were collected and relative abundance were related to trunk characteristics. Seasonal patterns of sandfly distribution in the forest were observed.