Relação entre fisiografia e solos desenvolvidos de material cenozoico da região do rio Jequitai, MG

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.

Crustáceos no cerrito Ariano Souza, Rio Grande, Rio Grande do Sul e distribuição de Callinectes sapidus (Brachyura, Portunidae)

While all species of the genus Callinectes Stimpson, 1860 have a continuous distribution on the Atlantic coast of the Americas, Callinectes sapidus Rathbun, 1896 is the only one with disjunct distribution. Considering that this species was introduced in Europe and Japan, it has been suggested that the occurrence of C. sapidus on the southern coast of Brazil was due to the transport by ballast water. In the archaeological site Ariano Souza, located in the estuary of the Patos Lagoon (southern Brazil), remains of crustaceans, including claws of approximately two thousand years ago, were found. A preliminary analysis of this material showed Callinectes chelae. Because this archaeological site is located inside the estuary, it has been hypothesized that these chelae belong either to C. sapidus or to C. danae Smith, 1869. A comparison between pincers collected in the archaeological and pincers of these two species (90 dactyls, 30 of each type) was performed. The analysis (ANOVA) considered the variability of seven characters of the dactyls, and demonstrated the existence of two groups. Results showed that the measured characters suffice to separate these species, and indicated that the material found in the archaeological site belongs to C. sapidus. The hypothesis of the introduction of C. sapidus in the area is rejected. The possible biogeographic history of the species is discussed.

Catalogue of the type material of Phasmatodea (Insecta) deposited in Brazilian museums

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.

Sôbre u'a modificação do meio de Monteverde

It is well known that the culture media used in the presumptive diagnosis of suspiciuous colonies from plates inoculated with stools for isolation of enteric organisms do not always correctly indicate the major groups of enterobacteria. In an effort to obtain a medium affording more exact indications, several media (1-9) have been tested. Modifications of some of these media have also been tested with the result that a satisfactory modification of Monteverde's medium was finaly selected. This proved to be most satisfactory, affording, as a result of only one inoculation, a complete series of basic indications. The modification involves changes in the formula, in the method of preparation and in the manner of storage. The formulae are: A. Thymol blue indicator: NaOH 0.1/N .............. 34.4 ml; Thymol blue .............. 1.6 g; Water .................... 65.6 ml. B. Andrade's indicator. C. Urea and sugar solution: Urea ..................... 20 g; Lactose ................... 30 g; Sucrose ................... 30 g; Water .................... 100 ml. The mixture (C.) should be warmed slightly in order to dissolve the ingredients rapidly. Sterilise by filtration (Seitz). Keep stock in refrigeratior. The modification of Monteverde's medium is prepared in two parts. Semi-solid part - Peptone (Difco) 2.0 g; NaCl 0.5 g; Agar 0.5 g; Water 100.0 ml. Boil to dissolve the ingredients. Adjust pH with NaOH to 7.3-7.4. Boil again for precipitation. Filter through cotton. Ad indicators "A" 0.3 ml and "B" 1.0 ml. Sterilise in autoclave 115ºC, 15 minutes in amounts not higher than 200 ml. Just before using, add solution "C" asseptically in amounts of 10 ml to 200 ml of the melted semi-solid medium, maintained at 48-50ºC. Solid part - Peptone (Difco) 1.5 g; Trypticase (BBL) 0.5 g; Agar 2.0 g; Water 100,00 ml. Boil to dissolve the ingredients. Adjust pH with NaOH to 7.3-7.4. Boils again. Filter through cotton. Add indicators "A" 0.3 ml and "B" 1.0 ml; ferrous ammonium sulfate 0.02 g; sodiun thiosulfate 0.02 g. Sterilise in autoclave 115ºC, 15 minutes in amounts not higher than 200 ml. Just before using, add solution "C" asseptically in amounts of 10 ml to 200 ml of the melted solid medium, maintained at 48-50ºC. Final medium - The semi-solid part is dispensed first (tubes about 12 x 120 mm) in 2.5 ml amounts and left to harden at room temperature, in vertical position. The solid part is dispensed over the hardened semi-solid one in amounts from 2.0 ml to 2.5 ml and left to harden in slant position, affording a butt of 12 to 15 mm. The tubes of medium should be subjected to a sterility test in the incubator, overnight. Tubes showing spontaneous gas bubbles (air) should then be discarded. The medium should be stored in the incubator (37ºC), for not more than 2 to 4 days. Storage of the tubes in the ice-box produces the absorption of air which is released as bubbles when the tubes are incubated at 37ºC after inoculation. This fact confirmed the observation of ARCHAMBAULT & McCRADY (10) who worked with liquid media and the aplication of their observation was found to be essential to the proper working conditions of this double-layer medium. Inoculation - The inoculation is made by means of a long straight needle, as is usually done on the triple sugar, but the needel should penetrate only to about half of the height of the semi-solid column. Indol detection - After inoculation, a strip of sterelized filter papaer previously moistened with Ehrlich's reagent, is suspended above the surface of the medium, being held between the cotton plug and the tube. Indications given - In addition to providing a mass of organisms on the slant for serological invetigations, the medium gives the following indications: 1. Acid from lactose and/or sucrose (red, of yellowsh with strains which reduce the indicators). 2. Gas from lactose and/or sucrose (bubbles). 3. H[2]S production, observed on the solid part (black). 4. Motility observed on the semi-solid part (tubidity). 5. Urease production, observed on solid and semi-solid parts (blue). 6. Indol production, observed on the strip of filter paper (red or purplish). Indol production is not observed with indol positive strains which rapidly acidify the surface o the slant, and the use of oxalic acid has proved to give less sensitive reaction (11). Reading of results - In most cases overnight incubation is enough; sometimes the reactions appear within only a few hours of incubation, affording a definitive orientation of the diagnosis. With some cultures it is necessary to observe the medium during 48 hours of incubation. A description showing typical differential reaction follows: Salmonella: Color of the medium unchanged, with blackening of the solid part when H[2]S is positive. The slant tends to alkalinity (greenish of bluish). Gas always absent. Indol negative. Motility positive or negative. Shigella: Color of the medium unchanged at the beginning of incubation period, but acquiring a red color when the strain is late lactose/sucrose positive. Slant tending to alkalinity (greenish or purplish). Indol positive or negative. Motility, gas and H[2]S always negative. Proteus: Color of the medium generally changes entirely to blue or sometimes to green (urease positive delayed), with blackening of solid part when H[2]S is positive. Motility positive of negative. Indol positive. Gas positive or negative. The strains which attack rapidly sucrose may give a yellow-greenish color to the medium. Sometimes the intense blue color of the medium renders difficult the reading of the H[2]S production. Escherichiae and Klebsiellae: Color of the medium red or yellow (acid) with great and rapid production of gas. Motility positive or negative. Indol generally impossible to observe. Paracoli: Those lactose of sucrose positive give the same reaction as Esherichia. Those lactose or sucrose negatives give the same reactions as Salmonellae. Sometimes indol positive and H[2]S negative. Pseudomonas: Color of the medium unchanged. The slant tends to alkalinity. It is impossible to observe motility because there is no growth in the bottom. Alkaligenes: Color of the medium unchanged. The slant tends to alkalinity. The medium does not alter the antigenic properties of the strains and with the mass of organisms on the slant we can make the serologic diagnosis. It is admitted that this medium is somewhat more laborious to prepare than others used for similar purposes. Nevertheless it can give informations generally obtained by two or three other media. Its use represents much saving in time, labor and material, and we suggest it for routine laboratory work in which a quick presumptive preliminary grouping of enteric organisms is needed.

Estudo dos megacarióticos em material humano

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.

Isolamento e caracterização de Pseudomonas maltophilia (Hugh & Ryschenkow, 1960) de material clínico humano, na cidade do Rio de Janeiro

Os autores estudaram as propriedades morfo-bioquímicas e a sensibilidade às substâncias antimicrobianas, de uma nova e rara espécie de Pseudomonas, a Pseudomonas maltophilia (Hugh & Ryschenkow, 1960), isolada de secração vaginal. Como características marcantes, dentre mais de 65 testadas, as amostras estudadas mostraram ser: oxidase negativa e lisina descarboxilase positiva; produziram desoxiribonuclease e um pigmento escuro que se difunde no meio; atacaram oxidativamente a maltose tanto em meio complexo nitrogenado como em meio de Hugh & Leifson e hidrolisaram a esculina. As amostras foram sensíveis ao cloranfenicol, gentamicina, kanamicina, colistin e gabromicina.

Immunopathology of Schistosoma mansoni infection in rabbits: (A preliminary report)

Five rabbits infected with Schistosoma mansoni showed marked resistance, which resulted in low worm recovery and low egg production. Pathological changes appeared in liver and intestines as scattered foci of eosinophilic infiltration around immature eggs, with only occasional granulomatous formation. Antibodies to ovular and adult worm structures were demonstrated by immunofluorescence in the sera of rabbits prior to infection (natural antibodies) and specially following infection by S. mansoni. These findings point out to the peculiarities of the immunopathology of schistosomiasis in rabbits.

Redescription of the type-material of creptotrema creptotrema travassos, Artigas & Pereira, 1928 (Digenea, Allocreadiidae)

Creptotrema creptotrema Travassos, Artigas & Pereira, 1928, a digenetic trematode parasite of Leporinus elongatus, is redescribed from the type-material with additional morphological data and original figures.

Levantamento preliminar de moluscos em praias arenosas e areno-lodosas de Piúma, estado do Espírito Santo, Brasil

The present work is a preliminary contribution to the knowledge of the fauna, with regard to the aspect of mullusks, on the coast located in the city of Piúma (40º45' lat. L and 20º50' long. W) Espírito Santo State, aiming a better comprehension of the distribution and ecology of mollusks in the South Atlantic. Collections were made in planned sporadic periods (May/29 to 31 of 1984; May/04-05 and September/13-16 of 1985; March/26-28; October/30-31 and November/01-02 of 1986), in the intertidal zones in the area, in each chosen region and in presence of an 0.0 tide. The material identified by comparative analysis of the morphologic variability presented a total of 41 generic taxa (52.56%) and 44 specific taxa (52.38%) of the class Gastropoda, 36 generic taxa (46.15%) and 39 specific taxa (46.43%) of the class Bivalvia and 1 generic taxa (1,28%) and 1 specific taxa (1.19%) of the class Scaphopoda.