A retarded coupling approach to intermolecular interactions

A wide range of physical phenomena such as optical binding and resonance energy transfer involve electronic coupling between adjacent molecules. A quantum electrodynamical description of these intermolecular interactions reveals the presence of retardation effects. The clarity of the procedure associated with the construction of the quantum amplitudes and the precision of the ensuing results for observable energies and rates are widely acknowledged. However, the length and complexity of the derivations involved in such quantum electrodynamical descriptions increase rapidly with the order of the process under study. Whether through the use of time-ordering approaches, or the more expedient state-sequence method, time-consuming calculations cannot usually be bypassed. A simple and succinct method is now presented, which provides for a direct and still entirely rigorous determination of the quantum electrodynamical amplitudes for processes of arbitrarily high order. Using the approach, new results for optical binding in two- and three-particle systems are secured and discussed

Germanene: a novel two-dimensional Germanium allotrope akin to Graphene and Silicene

Using a gold (111) surface as a substrate we have grown in situ by molecular beam epitaxy an atom-thin, ordered, two-dimensional multi-phase film. Its growth bears strong similarity with the formation of silicene layers on silver (111) templates. One of the phases, forming large domains, as observed in Scanning Tunneling Microscopy, shows a clear, nearly flat, honeycomb structure. Thanks to thorough synchrotron radiation core-level spectroscopy measurements and advanced Density Functional Theory calculations we can identify it to a $\sqrt{3}$x$\sqrt{3}$R(30{\deg}) germanene layer in coincidence with a $\sqrt{7}$x$\sqrt{7}$R(19.1{\deg}) Au(111) supercell, thence, presenting the first compelling evidence of the birth of a novel synthetic germanium-based cousin of graphene.Comment: 16 pages, 4 figures, 1 tabl

Raman scattering mediated by neighboring molecules

Raman scattering is most commonly associated with a change in vibrational state within individual molecules, the corresponding frequency shift in the scattered light affording a key way of identifying material structures. In theories where both matter and light are treated quantum mechanically, the fundamental scattering process is represented as the concurrent annihilation of a photon from one radiation mode and creation of another in a different mode. Developing this quantum electrodynamical formulation, the focus of the present work is on the spectroscopic consequences of electrodynamic coupling between neighboring molecules or other kinds of optical center. To encompass these nanoscale interactions, through which the molecular states evolve under the dual influence of the input light and local fields, this work identifies and determines two major mechanisms for each of which different selection rules apply. The constituent optical centers are considered to be chemically different and held in a fixed orientation with respect to each other, either as two components of a larger molecule or a molecular assembly that can undergo free rotation in a fluid medium or as parts of a larger, solid material. The two centers are considered to be separated beyond wavefunction overlap but close enough together to fall within an optical near-field limit, which leads to high inverse power dependences on their local separation. In this investigation, individual centers undergo a Stokes transition, whilst each neighbor of a different species remains in its original electronic and vibrational state. Analogous principles are applicable for the anti-Stokes case. The analysis concludes by considering the experimental consequences of applying this spectroscopic interpretation to fluid media; explicitly, the selection rules and the impact of pressure on the radiant intensity of this process

Interactions between spherical nanoparticles optically trapped in Laguerre-Gaussian modes

When a Laguerre-Gaussian (LG) laser mode is used to trap nanoparticles, the spatial disposition of the particles about the beam axis is determined by a secondary mechanism that engages the input radiation with the interparticle potential. This analysis, based on the identification of a range-dependent laser-induced energy shift, elicits and details features that arise for spherical nanoparticles irradiated by a LG mode. Calculations of the absolute minima are performed for LG beams of variable topological charge, and the results are displayed graphically. It is shown that more complex ordered structures emerge on extension to three- and four-particle systems and that similar principles will apply to other kinds of radially structured optical mode. © 2005 Optical Society of America

Profilaxia e controle do mal de cadeiras em animais domésticos no Pantanal.

O Trypanosoma evansi foi o primeiro tripanosoma patogênico descoberto. A surra, como a doença é conhecida na Índia, causada pelo T. evansi, há muitos séculos tem sido observada. Porém, foi somente em 1880 que Griffith Evans descobriu organismos móveis semelhantes a espirilos no sangue de cavalos e camelos doentes. Evans descreveu os parasitas em esfregaço frescos e os reconheceu como sendo protozoários. Evans acreditou que a fonte primária da infecção dos cavalos fossem as águas poluídas (Hoare, 1972).bitstream/item/81127/1/DOC66.pd

Optically induced forces and torques:Interactions between nanoparticles in a laser beam

Distinctive optical forces and torques arise between nanoparticles irradiated by intense laser radiation. These forces, associated with a pairwise process of stimulated scattering, prove to enable the possibility of producing significant modifications to both the form and magnitude of interparticle forces, with additional contributions arising in the case of dipolar materials. Moreover, such forces have the capacity to generate unusual patterns of nanoscale response, entirely controlled by the input beam characteristics- principally the optical frequency, intensity, and polarization. Based on quantum electrodynamical theory, a general result is secured for the laser-induced force under arbitrary conditions, incorporating both static and dynamic coupling mechanisms. Specific features of the results are identified for pairs of particles with prolate cylindrical symmetry, e.g., carbon nanotubes, where it is shown that the laser-induced forces and torques are sensitive functions of the pair spacing and orientation, and the laser beam geometry; significantly, they can be either repulsive or attractive according to conditions. For nanoparticles trapped in a Laguerre-Gaussian laser beam the results also reveal additional and highly distinctive torques that suggest further possibilities for nanomanipulation with light. The paper concludes with a discussion on several potential applications of such forces. © 2005 The American Physical Society

Influence of the state of light on the optically induced interparticle interaction

A general expression for the energy of interparticle interaction induced by an arbitrary mode of light is determined using quantum electrodynamics, and it is shown that the Casimir-Polder potential is included within this quantum result. Equations are also derived for the corresponding coupling induced by multimode number states of light, and the dependence of the pair energy on the Poynting vector and polarization state is determined. Attention is then focused on the interactions between particles trapped in counterpropagating coherent beams, both with and without interference, and it is shown that the results afford insights into the multiparticle structures that can be optically fabricated with counterpropagating input. Brief consideration is also given to the effect of squeezing the optical coherent state. Extending previous studies of optical binding in Laguerre-Gaussian beams, results are given for the case of particles trapped at radially different locations within the beam structure. Finally, consideration is given to interparticle interactions induced by broadband light, and it is shown how the length of optically fabricated particle chains can be controlled by the use of wavelength filters

Trypanosoma evansi e trypanosoma vivax: biologia, diagnóstico e controle.

Tripanosomoses; Taxonomia; Morfologia; Ciclo vital; Teminologia utiilzada para os tripanosomas baseada no Trypanosoma brucei; Manutenção dos Tripanosomas; Variação molecular em Tripanosomas; Ecologia e sociologia da variação antigênica; Genética de populações de Tripanosomas; Diagnóstico; Caracterização molecular; Métodos de controle; Resistência à drogas; Avaliação do uso do tratamento profilático estratégico ou curativo; Quimioterapia da Tripanosomose por Trypanosoma evansi (tratamento curativo); Quimioterapia da Tripanosomose por Trypanosoma vivax (tratamento curativo); Controle estratégico do Trypanosoma evansi através do uso de drogas tripanocidas; Controle estratégico do Trypanosoma vivax através do uso de drogas tripanocidas; Comparação do Isometamidium e Brometo de Homidium como droga profilática; Mecanismos experimentais de liberação lenta contendo Brometo de Homidium e Isometamidium; Análise econômica; Controle dos vetores; Controle através do uso de inseticidas; Piretroides; Utilização de armadilhas impregnadas com inseticidas