Self-consistent model for ambipolar tunneling in quantum-well systems

We present a self-consistent approach to describe ambipolar tunneling in asymmetrical double quantum wells under steady-state excitation and extend the results to the case of tunneling from a near-surface quantum well to surface states. The results of the model compare very well with the behavior observed in photoluminescence experiments in $InGaAs/InP$ asymmetric double quantum wells and in near-surface $AlGaAs/GaAs$ single quantum wells.Comment: 10 pages, REVTeX 3.

Near-field optical imaging and spectroscopy of a coupled quantum wire-dot structure

A coupled GaAs/AlGaAs quantum wire (QWR)-dot sample grown by molecular beam epitaxy on a patterned (311)A GaAs substrate is studied by near-field spectroscopy at a temperature of 10 K with a spectral resolution of 100 µeV. The two-dimensional potential energy profiles of the sample including localized excitonic states caused by structural disorder are determined in photoluminescence measurements with a spatial resolution of 150 nm. One finds a potential barrier of 20 meV between the quantum wire and the embedding quantum well (QW) on the mesa top of the structure. This is due to local thinning of the GaAs layer. In contrast, the wire-dot interface results free of energy barriers. The spatial variation of the GaAs layer thickness provides information on the growth mechanism determined by lateral diffusion of Ga atoms which is modeled by an analytical model. By performing spatially resolved photoluminescence excitation measurements on this wire-dot structure, we present a method for investigating carrier transport in low-dimensional systems: The dot area is used as an optical marker for excitonic diffusion via QW and QWR states. The two-dimensional (2D) and 1D diffusion coefficients are extracted as a function of the temperature and discussed

Network analysis of plasmidomes: the Azospirillum brasilense Sp245 case

Azospirillum brasilense is a nitrogen-fixing bacterium living in association with plant roots. The genome of the strain Sp245, isolated in Brazil from wheat roots, consists of one chromosome and six plasmids. In this work, the A. brasilense Sp245 plasmids were analyzed in order to shed some light on the evolutionary pathways they followed over time. To this purpose, a similarity network approach was applied in order to identify the evolutionary relationships among all the A. brasilense plasmids encoded proteins; in this context a computational pipeline specifically devoted to the analysis and the visualization of the network-like evolutionary relationships among different plasmids molecules was developed. This information was supplemented with a detailed (in silico) functional characterization of both the connected (i.e., sharing homology with other sequences in the dataset) and the unconnected (i.e., not sharing homology) components of the network. Furthermore, the most likely source organism for each of the genes encoded by A. brasilense plasmids was checked, allowing the identification of possible trends of gene loss/gain in this microorganism. Data obtained provided a detailed description of the evolutionary landscape of the plasmids of A. brasilense Sp245, suggesting some of the molecular mechanisms responsible for the present-day structure of these molecules

Temperature-dependent near-field imaging of delocalized and localized excitons in single quantum wires

Summary form only given. Recent microphotoluminescence studies have shown that the low-temperature emission spectra of semiconductor quantum wires are dominated by localized, quasi-zero-dimensional, excitons. This implies that both the optical and transport properties of such quasi-one-dimensional (Q1D) nanostructures are similar to that of a chain of quantum dots. It also hinders the observation of some truly one-dimensional quantum effects, such as the ballistic or diffusive one-dimensional exciton transport, expected in nanostructures containing Q1D excitons that are delocalized over mesoscopic length scales. We present the first experimental evidence for such delocalized excitons in a single quantum wire. A novel coupled quantum wire-dot nanostructure is studied by low temperature near-field photoluminescence (PL) spectroscopy

Opportunities for Technology and Tool Development: Understanding the Brain as a Whole

Major resources are now available to develop tools and technologies aimed at dissecting the circuitry and computations underlying behavior, unraveling the underpinnings of brain disorders, and understanding the neural substrates of cognition. Scientists from around the world shared their views around new tools and technologies to drive advances in neuroscience

Construyendo la solución paso a paso

En su discurso en la conferencia de lacea, en 2011, el economista Sendhil Mullainathan, de la Universidad de Harvard, explicaba que existe una conexión muy simple entre la pobreza y el comportamiento humano; un nexo que nos ayuda a comprender la aparente irracionalidad en muchas de las decisiones que toman los pobres. Al estar bajo condiciones de extrema necesidad, el ser hu-mano enfoca la mayor parte de sus pensamientos en esta situación, de manera que disminuyen sus capacidades cognitivas en el resto de actividades, incluido el autocontrol. Esto, que ha sido verificado empíricamente tanto en el campo como en el laboratorio, lleva a que los pobres tomen peores decisiones que los demás, con el agravante de que, en su caso, una mala decisión puede tener consecuencias desastrosas y permanentes. Este es solo un ejemplo de los grandes aportes que se han dado en la intersección de la economía y la psicología, y que van en contravía de los modelos construidos por los economistas de Occidente

All-Optical Interrogation of Neural Circuits

There have been two recent revolutionary advances in neuroscience: First, genetically encoded activity sensors have brought the goal of optical detection of single action potentials in vivo within reach. Second, optogenetic actuators now allow the activity of neurons to be controlled with millisecond precision. These revolutions have now been combined, together with advanced microscopies, to allow “all-optical” readout and manipulation of activity in neural circuits with single-spike and single-neuron precision. This is a transformational advance that will open new frontiers in neuroscience research. Harnessing the power of light in the all-optical approach requires coexpression of genetically encoded activity sensors and optogenetic probes in the same neurons, as well as the ability to simultaneously target and record the light from the selected neurons. It has recently become possible to combine sensors and optical strategies that are sufficiently sensitive and cross talk free to enable single-action-potential sensitivity and precision for both readout and manipulation in the intact brain. The combination of simultaneous readout and manipulation from the same genetically defined cells will enable a wide range of new experiments as well as inspire new technologies for interacting with the brain. The advances described in this review herald a future where the traditional tools used for generations by physiologists to study and interact with the brain—stimulation and recording electrodes—can largely be replaced by light. We outline potential future developments in this field and discuss how the all-optical strategy can be applied to solve fundamental problems in neuroscience.Chemistry and Chemical Biolog

Looking at Localized Excitons in Quantum Structures: A Theoretical Description

We present a theory of scanning local optical spectroscopy in quantum structures taking into account structural disorder. The calculated spatially resolved spectra show the individual spectral lines from the exciton states localized by the disordered potential as well as the quasicontinua spectra at positions close to the potential barriers in agreement with the experimental findings

Impact of CFTR Modulators on Beta-Cell Function in Children and Young Adults with Cystic Fibrosis

Background: To date, no consistent data are available on the possible impact of CFTR modulators on glucose metabolism. The aim of this study was to test the hypothesis that treatment with CFTR modulators is associated with an improvement in the key direct determinants of glucose regulation in children and young adults affected by Cystic Fibrosis (CF). Methods: In this study, 21 CF patients aged 10–25 underwent oral glucose tolerance test (OGTT) before and after 12–18 months of treatment with Lumacaftor/Ivacaftor or Elexacaftor-Ivacaftor-Tezacaftor. β-cell function (i.e., first and second phase of insulin secretion measured as derivative and proportional control, respectively) and insulin clearance were estimated by OGTT mathematical modelling. Insulin sensitivity was estimated by the Oral Glucose Sensitivity Index (OGIS). The dynamic interplay between β-cell function, insulin clearance and insulin sensitivity was analysed by vector plots of glucose-stimulated insulin bioavailability vs. insulin sensitivity. Results: No changes in glucose tolerance occurred after either treatment, whereas a significant improvement in pulmonary function and chronic bacterial infection was observed. Beta cell function and insulin clearance did not change in both treatment groups. Insulin sensitivity worsened in the Lumacaftor/Ivacaftor group. The analysis of vector plots confirmed that glucose regulation was stable in both groups. Conclusions: Treatment of CF patients with CFTR modulators does not significantly ameliorate glucose homeostasis and/or any of its direct determinants