Strain balanced quantum posts

Quantum posts are assembled by epitaxial growth of closely spaced quantum dot layers, modulating the composition of a semiconductor alloy, typically InGaAs. In contrast with most self-assembled nanostructures, the height of quantum posts can be controlled with nanometer precision, up to a maximum value limited by the accumulated stress due to the lattice mismatch. Here we present a strain compensation technique based on the controlled incorporation of phosphorous, which substantially increases the maximum attainable quantum post height. The luminescence from the resulting nanostructures presents giant linear polarization anisotropy.Comment: Submitted to Applied Physics Letters (7th March 2011). 4 pages, 4 figure

The Gypsy Database (GyDB) of mobile genetic elements: release 2.0

This article introduces the second release of the Gypsy Database of Mobile Genetic Elements (GyDB 2.0): a research project devoted to the evolutionary dynamics of viruses and transposable elements based on their phylogenetic classification (per lineage and protein domain). The Gypsy Database (GyDB) is a long-term project that is continuously progressing, and that owing to the high molecular diversity of mobile elements requires to be completed in several stages. GyDB 2.0 has been powered with a wiki to allow other researchers participate in the project. The current database stage and scope are long terminal repeats (LTR) retroelements and relatives. GyDB 2.0 is an update based on the analysis of Ty3/Gypsy, Retroviridae, Ty1/Copia and Bel/Pao LTR retroelements and the Caulimoviridae pararetroviruses of plants. Among other features, in terms of the aforementioned topics, this update adds: (i) a variety of descriptions and reviews distributed in multiple web pages; (ii) protein-based phylogenies, where phylogenetic levels are assigned to distinct classified elements; (iii) a collection of multiple alignments, lineage-specific hidden Markov models and consensus sequences, called GyDB collection; (iv) updated RefSeq databases and BLAST and HMM servers to facilitate sequence characterization of new LTR retroelement and caulimovirus queries; and (v) a bibliographic server. GyDB 2.0 is available at http://gydb.org

IMPORTANCE OF DIETARY TAURINE AND SELENIUM ON GROWTH AND SURVIVAL OF ATLANTIC BLUEFIN TUNA Thunnus thynnus LARVAE

One of the most important bottleneck in the farming of Atlantic bluefin tuna (ABT) is the growth and survival during the larval rearing phase, mainly related with the diet quality. For the last ten years the Spanish Institute of Oceanography (IEO) in Mazarrón (Murcia, SE Spain) has developed a technique for ABT larval rearing and juvenile production. Taurine and selenium are essential water soluble compounds in live preys and inert diets for ABT larvae and juveniles. To know the importance of dietary taurine and selenium on growth and survival of ABT larvae, two experiments have been carried out with different taurine (Exp1) and selenium (Selplex® ) (Exp2) doses added to rotifers enriched with ALGAMAC 3050® . Both experiments were finished at 14 days post hatching. ABT fertilized eggs were collected from captive breeders spawning spontaneously in floating cages in the area. The eggs, transported to the IEO facilities, were quantified, cleaned, selected by buoyancy and distributed randomly in 1400 L fiber cylindrical glass tanks at a density of 10 ABT eggs per liter, whereas prey density was maintained at 5 rotifers per mL. Temperature ranges were: 24.0±0.5ºC and 26.0±0.5ºC for Exp1 and Exp2, respectively. Fig 1 shows the growth results in size for both experiments at 14 dph. Survival in both cases was close to 10% with no significant differences due to the different treatments. The lowest growth in size was observed in larvae fed dose 0 in both experiments Standard length average (mm ± confidence intervals) in Exp1 and Exp2 at 14 dph. Letters indicate statistically significant differences (95%

High-strain deformation of conglomerates: Numerical modelling, strain analysis, and an example from the Wutai Mountains, North China Craton

Conglomerates have been widely used to investigate deformation history and rheology, strain, vorticity and viscosity. Previous studies reveal that several factors, such as pebble shapes and concentrations, as well as material properties, affect conglomerate deformation. However, how pebble concentration and interaction between pebbles affect deformation is not understood very well. We use the 2D numerical modelling platform ELLE coupled to the full field crystal visco-plasticity code (VPFFT) to simulate the deformation of conglomerates with various viscosity contrasts between pebbles and matrix and different pebble concentrations, with both linear (stress exponent n = 1) and power-law (n = 3) viscous rheologies, under simple shear conditions up to a shear strain of ten. Pebbles can behave as effectively passive, deformable or effectively rigid. An increase in pebble concentrations/viscosity contrasts enhances pebble deformation, but reduces their rotation. A mean aspect ratio (Rf) - orientation (ϕ) plot is proposed to gain an estimate of pebble deformation behaviour and the amount of bulk strain. Closely spaced rigid or deformable pebbles can form clusters that mechanically act as single inclusions. Rigid clusters rotate and survive for only short strain increments, whereas the more stable deformable ones keep on elongating with minor rotation. We provide a natural example of deformed conglomerates from the Wutai Mountains, North China Craton. These consist of banded-iron-formation (BIF) pebbles embedded in a schistose matrix. Using the mean Rf-ϕ plot, a finite strain of ∼6 under simple shear could be determined. The viscosity of the pebbles is estimated at about 5-8 times that of the matrix for a linear rheology (n = 1), or 2 to 5 times if a power-law rheology with n = 3 is assumed

Europe, listen and respond. Enhancing the European Commission´s online public consultation tool.

Fac. de Ciencias de la InformaciónFALSEpu

Recent trends in molecular diagnostics of yeast infections : from PCR to NGS

The incidence of opportunistic yeast infections in humans has been increasing over recent years. These infections are difficult to treat and diagnose, in part due to the large number and broad diversity of species that can underlie the infection. In addition, resistance to one or several antifungal drugs in infecting strains is increasingly being reported, severely limiting therapeutic options and showcasing the need for rapid detection of the infecting agent and its drug susceptibility profile. Current methods for species and resistance identification lack satisfactory sensitivity and specificity, and often require prior culturing of the infecting agent, which delays diagnosis. Recently developed high-throughput technologies such as next generation sequencing or proteomics are opening completely new avenues for more sensitive, accurate and fast diagnosis of yeast pathogens. These approaches are the focus of intensive research, but translation into the clinics requires overcoming important challenges. In this review, we provide an overview of existing and recently emerged approaches that can be used in the identification of yeast pathogens and their drug resistance profiles. Throughout the text we highlight the advantages and disadvantages of each methodology and discuss the most promising developments in their path from bench to bedside

Persistent Currents in Small, Imperfect Hubbard Rings

We have done a study with small, imperfect Hubbard rings with exact diagonalization. The results for few-electron rings show, that the imperfection, whether localized or not, nearly always decrease, but can also \emph{increase} the persistent current, depending on the character of the imperfection and the on-site interaction. The calculations are generally in agreement with more specialized studies. In most cases the electron spin plays an important role.Comment: 6 pages, 4 figure

Somatostatin subtype-2 receptor-targeted metal-based anticancer complexes

Conjugates of a dicarba analogue of octreotide, a potent somatostatin agonist whose receptors are overexpressed on tumor cells, with [PtCl 2(dap)] (dap = 1-(carboxylic acid)-1,2-diaminoethane) (3), [(η 6-bip)Os(4-CO 2-pico)Cl] (bip = biphenyl, pico = picolinate) (4), [(η 6-p-cym)RuCl(dap)] + (p-cym = p-cymene) (5), and [(η 6-p-cym)RuCl(imidazole-CO 2H)(PPh 3)] + (6), were synthesized by using a solid-phase approach. Conjugates 3-5 readily underwent hydrolysis and DNA binding, whereas conjugate 6 was inert to ligand substitution. NMR spectroscopy and molecular dynamics calculations showed that conjugate formation does not perturb the overall peptide structure. Only 6 exhibited antiproliferative activity in human tumor cells (IC 50 = 63 ± 2 μ in MCF-7 cells and IC 50 = 26 ± 3 μ in DU-145 cells) with active participation of somatostatin receptors in cellular uptake. Similar cytotoxic activity was found in a normal cell line (IC 50 = 45 ± 2.6 μ in CHO cells), which can be attributed to a similar level of expression of somatostatin subtype-2 receptor. These studies provide new insights into the effect of receptor-binding peptide conjugation on the activity of metal-based anticancer drugs, and demonstrate the potential of such hybrid compounds to target tumor cells specifically. © 2012 American Chemical Society