Resumo Nesse estudo, descrevemos a diversidade de Mesembrinelinae, em uma reserva biológica na cidade de Nova Iguaçu, Estado do Rio de Janeiro. Armadilhas contendo sardinha foram distribuídas sazonalmente em quatro pontos: Ponto A (22° 58.788’ S, 43° 43.459’ W), na borda da mata B (22° 58.523’ S, 43° 44.540’ W), C (22° 58.350’ S, 43° 44.678’ W), e D (22° 34.865’ S, 43º 27.063’ W), localizados a 1.000m, 500m e 2.000m para o interior da borda respectivamente. Foram coletados 2.159 exemplares de Mesembrinellinae, com um total de dez espécies. Laneela nigripes Guimarães, 1977 foi a espécie mais abundante, seguida por Mesembrinella bellardiana Aldrich, 1922, Eumesembrinella cyaneicincta (Surcouf, 1919) e Mesembrinella semihyalina Mello, 1967. Essas espécies foram consideradas comuns e contantes durante o período de estudo. Mesembrinella batesi Aldrich, 1922, Eumesembrinella quadrilineata Fabricius, 1805 e Huascaromusca aeneiventris (Wiedmann, 1830) foram as moscas com as menores abundâncias, sendo consideradas raras e acidentais, Eumesembrinella besnoiti (Seguy, 1925) foi rara e acessória. Eumesembrinella cyaneicincta, M. bellardiana, M. semihyalina e M. bicolor foram as mais coletadas no ponto B, enquanto L. nigripes foi a mais coletada no ponto C. Os efeitos de borda não foram evidentes porque os quatro pontos apresentaram populações similares. O ponto B apresentou uma relação forte e positiva entre a abundância e a riqueza, no ponto C a correlação foi positiva e fraca e não houve correlação nos pontos A e D. A maior abundância de indivíduos foi registrada nas estações do outono e inverno. Espécimes da subfamília Mesembrinellinae ocorreram da borda até 2.000 metros para o interior da mata.

Abstract In this study we describe the diversity of Mesembrinelinae in a biological reserve in the city of Nova Iguaçu, State of Rio de Janeiro. Traps containing sardines were distributed seasonally, at four sites: Site A (22° 58.788’ S, 43° 43.459’ W), in a forest edge, and sites B (22° 58.523’ S, 43° 44.540’ W), C (22° 58.350’ S, 43° 44.678’ W), and D (22° 34.865’ S, 43° 27.063’ W), located 1,000m, 500m, and 2,000m respectively, inwards from the edge. A total of 2,150 individuals of Mesembrinellinae were collected, representing ten species. Laneela nigripes Guimarães, 1977 was the most abundant species, followed by Mesembrinella bellardiana Aldrich, 1922, Eumesembrinella cyaneicincta (Surcouf, 1919) and Mesembrinella semihyalina Mello, 1967. These species were common and constant during the study period. Mesembrinella batesi Aldrich, 1922, Eumesembrinella quadrilineata (Fabricius, 1805) and Huascaromusca aeneiventris (Wiedmann, 1830) were the less abundant flies, being considered rare and accidental. Eumesembrinella besnoiti (Seguy, 1925) was rare and accessory. Eumesembrinella cyaneicincta, M. bellardiana, M. semihyalina and M. bicolor were mostly collected in site B, while L. nigripes was mostly collected in site C. The edge effect was not evident since the four sites showed similar populations. Site B showed a strong positive relationship between abundance and richness, in site C the correlation was positive and weak, and there was no correlation in A and D. The highest abundance of specimens was recorded during autumn and winter. These flies occurred from the edge up to 2,000m inside the forest.

With a view to contribute to the understanding the surface effects on optical properties process, and its hole in the electronic properties of the nanoparticles, CdS based nanoparticles are characterised by different experimental techniques and the experimental results compared to density functional theory calculations. Our results indicate that cubic CdS nanoparticles present a strong structural deformation, hexagonal reconstructed structures preserve their lattice behaviour. Both cubic and hexagonal CdS nanoparticles are S-terminated after relaxation, even when mildly Cd-rich nanoparticles are considered. A broad peak observed in our PL measurements is interpreted as an experimental evidence of the surface related peak observed around 1.8 eV in our calculated DOS for the hexagonal relaxed structure.

In this work we employ the state of the art pseudopotential method, within a generalized gradient approximation to the density functional theory, to investigate the dissociative adsorption process of glycine on the silicon surface. Our total energy calculations indicate that the chemisorption of the molecule is as follow. The gas phase NH2-C2H2-OOH adsorbs molecularly to the electrophilic surface Si atom and then dissociates into NH2-C2H2-OO and H, bonded to the electrophilic and nucleophilic surface silicon dimer atoms respectively, with an energy barrier corresponding to a thermal activation that is smaller than the usual growth temperature, indicating that glycine molecules will be observed in their dissociated states at room temperature. This picture is further support by our calculated vibrational modes for the considered adsorbed species.

Using a first-principles pseudopotential technique within a generalized gradient approximation of the density functional theory, we have investigated the mechanism of adsorption of molecular oxygen on the CdTe(110) surface. The determination of the more favorables structures and their formation through the activation barrier analysis indicates that the formation can occur in the regimes of low and high temperatures. According to our calculations it was verified that in the regime of low temperatures the oxygen molecule binds exclusively to Cd at the topmost site through Cd-O-O or Cd-O2 bonds. The electronic band structure presents a characteristic state like a double acceptor defect. In the high temperature regime the molecule adsorbs between Cd of the surface and Te of the subsurface, breaking Cd-Te bond and causing an upward dislocation of Cd from the subsurface. In this regime of high temperatures the complex presents Cd-O, Cd-O2, Te-O and O-O bonds and the electronic band structure is almost free of gap of states.

The present work is a comparative study of possible adsorption structures of the conjugated molecule acrylonitrile on Si(001) employing the state of the art pseudopotential method, within a generalized gradient approximation to the density functional theory. In the recent literature it is proposed the interaction of acrylonitrile with Si(001) through a cycloaddition reaction of the cyano group, in competition with the bounding of the two outer atoms of the molecule skeleton with the Si dimer in cross-dimer and cross-trench geometries; between other geometries like which correspond the reaction of the C = C bond with a Si dimer. Starting from a large number of configurations our calculations favor the planar cycloaddition through the terminal N and C atoms on the Si dimer. In this way we explain the electronic and vibrational features obtained experimentally.

In this work we employ the state of the art pseudopotential method, within a generalized gradient approximation to the density functional theory, to investigate the adsorption process of acetonitrile on the silicon surface. Our first-principles calculations indicate that CH3CN adsorbs via a [2+2] cycloaddition reaction through the C<FONT FACE=Symbol>º</FONT>N group with an adsorption energy around 35 kcal/mol, close to the 30 kcal/mol estimated by Tao and co-workers. The electronic structure and the surface states calculated for the adsorbed system are also discussed.

The adsorption of maleic anhydride on the Si(001) surface was investigated using the first-principles pseudopotential formalism. Our results indicate that C2H2-C2O3 adsorbs through a [2+2] cycloaddition of the C-C bond to the dangling bonds of Si-Si dimers, as observed for other small hydrocarbons. According to our calculations, the adsorption of a second maleic anhydride molecule will preferentially occur on first-neighbours Si-Si dimer sites in either the dimer chain our dimer row, i.e. considering a (4×2) reconstruction, C2H2-C2O3 can either form a linear chain or a zig-zag chain, depending on the growth conditions. Although both structures are found to be stable from the energetic point of view, only our STM theoretical images for the linear chain are comparable to available experimental data.

Using a first-principles pseudopotential method we have compared the adsorption and dissociation of the common n-type dopant molecule PH3 on the Si(001)-(21) and Ge(001){(21) surfaces. We find that the dissociated state is energetically more favourable than the molecular state by 1.70(0.81) eV, whereas the latter is 0.58(0.25) eV more stable than the system composed of the free silicon(germanium) surface and PH3(g). The chemisorbed system is characterised by elongated Si{Si(Ge{Ge) dimers that are symmetric in the dissociative case and asymmetric in the molecular case and by the fact that the Si(Ge){PH2 as well as the PH3(ads) groups retain the pyramidal geometry of the phosphine molecule. Our dissociative adsorption model is further supported by our calculated vibrational modes, which are in good agreement with available experimental works.

The atomic geometry, chemical bonding and energetics for full -, 2/3, 1/2 and 1/3 of a monolayer of Te coverages on the Si(001)/Te -(1 x 1), (2 x 1), and (3 x 1) surfaces have been studied employing first - principles total-energy calculations. For one monolayer coverage we nd that the (1 x 1) structure is energetically favourable against (2 x 1) structure, in agreement with experimental results, indicating that the dimerization of Te atoms is not an exothermic process. For a coverage of 2/3 of a monolayer, the formation of Te-Si-Te mixed trimers, in a (3 x 1) - reconstruction, is an energetically stable configuration. At 1/3 coverage, we have obtained the formation of Si-Si dimers with a single Te atom, at the surface in a (3 x 1) - reconstruction. In this structure there is a very weak interaction between the dimer and the single Te atom.

We investigate the stability and electronic structure of 1×2 and 2×2 GaAs(001):Te and InAs(001):Te surfaces with different degrees of tellurium coverage (thetaTe = <img src="http:/img/fbpe/bjp/v29n4/a4414.gif" alt="a4414.gif (106 bytes)" align="absmiddle">, <img src="http:/img/fbpe/bjp/v29n4/a4412.gif" alt="a4412.gif (100 bytes)" align="absmiddle">, <img src="http:/img/fbpe/bjp/v29n4/a4434.gif" alt="a4434.gif (104 bytes)" align="absmiddle">, 1), by means of rst-principles pseudopotential calculations within density-functional theory. The adsorption stability decreases as the tellurium coverage increases. The adsorption on InAs(001) is more stable than on GaAs(001). As-Ga (or As-In) bonds for the uppermost As atoms are s²p² -like (nearly planar), while the Te bonds at the surfaces are sp³-like. The hetero-dimers in thetaTe = <img src="http:/img/fbpe/bjp/v29n4/a4412.gif" alt="a4412.gif (100 bytes)" align="absmiddle"> modify the character of GaAs(001):Te and InAs(001):Te surfaces resulting in a semiconductor structure.

A actinomicose do sistema nervoso central (SNC) é afecção rara, caracterizada pela formação de abscesso único e de evolução crônica. Os autores descrevem o caso de um paciente jovem, imunocompetente, com actinomicose cerebral oriunda de foco primário cervicofacial, submetido a ressecção cirúrgica e antibioticoterapia. Ressalta-se a importância do conhecimento da entidade e de suas principais formas de acometimento, como a base do diagnóstico precoce dessa enfermidade potencialmente curável e de bom prognóstico.

Central nervous system actinomycosis is a rare but treatable chronic suppurative bacterial infection. The case of a young immunocompetent male with actinomycosis of the CNS is presented. The abscess originated from a primary cervico-facial infection and was located in the left parasellar region. After excision of the mass, that showed Actinomyces colonies, the patient was treated with intravenous Penicillin for 42 days followed by oral administration of the drug for 30 days. After surgery the patient was left with mild sequelae that had improved by the last follow-up, 7 months later. A new CT scan at that time revealed no residual disease or recurrence. The early diagnosis of cerebral actinomycosis relies essentially on a clinical suspicion. Hence it is imperative to be aware of the natural history of this infection and its various modes of presentation.