Consistência hidrológica de modelos digitais de elevação (MDE) para definição da rede de drenagem na sub-bacia do horto florestal Terra Dura, Eldorado do Sul, RS

O desenvolvimento da erosão hídrica ocorre em resposta ao modo como a água se move através e sobre uma determinada paisagem. O modelo digital de elevação (MDE) deve, portanto, ser o mais preciso possível, uma vez que constitui a base para a análise do relevo. Este trabalho teve como objetivo definir um modelo digital de elevação hidrologicamente consistente (MDEHC) e o método de direção de fluxo mais adequado para a definição da rede de drenagem na sub-bacia do horto florestal Terra Dura, município de Eldorado do Sul, RS. Foram testados os modelos gerados com os interpoladores Topogrid e redes triangulares irregulares (Triangulated Irregular Network -TIN) linear (TIN L) e TIN natural neighbor (TIN NN). A qualidade em relação às análises hidrológicas foi avaliada por meio da comparação das curvas de nível geradas pelos modelos testados com as curvas originais da sub-bacia (escala 1:10.000); da avaliação da quantidade de áreas planas; e da comparação da drenagem gerada pelos modelos a partir dos métodos de direção de fluxo Deterministic (D8) e Deterministic infinity (D∞ ou D infinito) com a drenagem original. Entre os modelos avaliados, o Topogrid apresentou maior consistência hidrológica, verificada na melhor continuidade das curvas de nível (menos arestas) e maior detalhamento da área de drenagem e divisores, acarretando menor quantidade de áreas planas e caminhos de fluxo mais detalhados, independentemente do método de direção de fluxo utilizado. Em relação à rede de drenagem, o método distribuído D∞ obteve melhor desempenho na descrição dos caminhos de fluxo, comparado ao método de direção única D8. O MDEHC Topogrid associado ao método D∞ proporcionou a identificação mais precisa dos caminhos preferenciais do fluxo que formam a rede de drenagem.

Vortex state and effect of anisotropy in sub-100 nm magnetic nanodots

Magnetic properties of Fe nanodots are simulated using a scaling technique and Monte Carlo method, in good agreement with experimental results. For the 20-nm-thick dots with diameters larger than 60¿nm, the magnetization reversal via vortex state is observed. The role of magnetic interaction between dots in arrays in the reversal process is studied as a function of nanometric center-to-center distance. When this distance is more than twice the dot diameter, the interaction can be neglected and the magnetic properties of the entire array are determined by the magnetic configuration of the individual dots. The effect of crystalline anisotropy on the vortex state is investigated. For arrays of noninteracting dots, the anisotropy strongly affects the vortex nucleation field and coercivity, and only slightly affects the vortex annihilation field

Different behaviour of mouse-human chimeric antibody F(ab')2 fragments of IgG1, IgG2 and IgG4 sub-class in vivo.

Mouse-human chimeric monoclonal antibodies (MAbs) of 3 different human IgG sub-classes directed against carcinoembryonic antigen (CEA) have been produced in SP-0 cells transfected with genomic chimeric DNA. F(ab')2 fragments were obtained by pepsin digestion of the purified chimeric MAbs of human IgG1, IgG2 and IgG4 sub-class and of parental mouse MAb IgG1. The 4 F(ab')2 fragments exhibit similar molecular weight by SDS-PAGE. They were labelled with 125I or 131I and high binding (80 to 87%) to purified unsolubilized CEA was observed. In vivo, double labelling experiments indicate that the longest biological half-life and the highest tumour-localization capacity is obtained with F(ab')2 from chimeric MAb of human IgG2 sub-class, whereas F(ab')2 from chimeric MAb IgG4 give very low values for these 2 parameters. F(ab')2 from chimeric MAb IgG1 and from parental mouse MAb yield intermediate results in vivo. Our findings should help to select the appropriate human IgG sub-class to produce chimeric or reshaped MAb F(ab')2 to be used for tumour detection by immunoscintigraphy and for radioimmunotherapy.

Contribution of (sub)domains of Staphylococcus aureus fibronectin-binding protein to the proinflammatory and procoagulant response of human vascular endothelial cells.

The Staphylococcus aureus fibronectin (Fn) -binding protein A (FnBPA) is involved in bacterium-endothelium interactions which is one of the crucial events leading to infective endocarditis (IE). We previously showed that the sole expression of S. aureus FnBPA was sufficient to confer to non-invasive Lactococcus lactis bacteria the capacity to invade human endothelial cells (ECs) and to launch the typical endothelial proinflammatory and procoagulant responses that characterize IE. In the present study we further questioned whether these bacterium-EC interactions could be reproduced by single or combined FnBPA sub-domains (A, B, C or D) using a large library of truncated FnBPA constructs expressed in L. lactis. Significant invasion of cultured ECs was found for L. lactis expressing the FnBPA subdomains CD (aa 604-877) or A4(+16) (aa 432-559). Moreover, this correlates with the capacity of these fragments to elicit in vitro a marked increase in EC surface expression of both ICAM-1 and VCAM-1 and secretion of the CXCL8 chemokine and finally to induce a tissue factor-dependent endothelial coagulation response. We thus conclude that (sub)domains of the staphylococcal FnBPA molecule that express Fn-binding modules, alone or in combination, are sufficient to evoke an endothelial proinflammatory as well as a procoagulant response and thus account for IE severity.

Sub-inhibitory concentrations of vancomycin prevent quinolone-resistance in a penicillin-resistant isolate of Streptococcus pneumoniae.

BACKGROUND: The continuous spread of penicillin-resistant pneumococci represents a permanent threat in the treatment of pneumococcal infections, especially when strains show additional resistance to quinolones. The main objective of this study was to determine a treatment modality impeding the emergence of quinolone resistance. RESULTS: Exposure of a penicillin-resistant pneumococcus to increasing concentrations of trovafloxacin or ciprofloxacin selected for mutants resistant to these drugs. In the presence of sub-inhibitory concentrations of vancomycin, development of trovafloxacin-resistance and high-level ciprofloxacin-resistance were prevented. CONCLUSIONS: Considering the risk of quinolone-resistance in pneumococci, the observation might be of clinical importance.

leges Wisigothorum : conjectae inter lineas et ad marginem glossae ; initio et sub finem nonnulla desiderantur

Colbertinus

decisiones Rotae ab anno 1376. ad annum 1381. sub certis capitulis digestae : authore Guillelmo Herboch, sacri palatii causarum Auditore

Philiberti de la Mare