Cotauberian Operators on L1(0, 1) Obtained by Lifting

ABSTRACT:We show that the set Td(L1(0, 1)) of cotauberian operators acting on L1(0, 1) is not open, and T ? Td(L1(0, 1)) does not imply T** cotauberian. As a consequence, we derive that the set T(L8(0, 1)) of tauberian operators acting on L8(0, 1) is not open, and that T ? T(L8(0,1)) does not imply T** tauberian

A Coupled Electrical-Thermal-Mechanical Modeling of Gleeble Tensile Tests for Ultra-High-Strength (UHS) Steel at a High Temperature

International audienceA coupled electrical-thermal-mechanical model is proposed aimed at the numerical modeling of Gleeble tension tests at a high temperature. A multidomain, multifield coupling resolution strategy is used for the solution of electrical, energy, and momentum conservation equations by means of the finite element method. Its application to ultra-high-strength steel is considered. After calibration with instrumented experiments, numerical results reveal that significant thermal gradients prevail in Gleeble tensile steel specimen in both axial and radial directions. Such gradients lead to the heterogeneous deformation of the specimen, which is a major difficulty for simple identification techniques of constitutive parameters, based on direct estimations of strain, strain rate, and stress. The proposed direct finite element coupled model can be viewed as an important achievement for subsequent inverse identification methods, which should be used to identify constitutive parameters for steel at a high temperature in the solid state and in the mushy state

The effect of aluminium on twinning in binary alpha-titanium

The deformation mechanisms of binary Ti–Al model alloys (0–13.1 at.% Aluminium) have been investigated with respect to the twinning activity using in-situ loading in combination with neutron diffraction as well as detailed post mortem electron backscatter diffraction analysis. A consistent starting grain size and texture was generated for all alloys promoting tensile twinning during compression testing. Long-wavelength neutron diffraction and selected area diffraction transmission electron microscopy analysis were carried out to detect evidence of Aluminium ordering and Ti3Al formation.It was found that raising the Aluminium content in Titanium does first slightly enhance twinning, with {10View the MathML source2} tensile twinning being by far the dominant type, while the critical residual intergranular strains for twin initiation decreases. This suggests that either the lowering of stacking fault energy by Aluminium or its solute solution strengthening effect are important factors. At around 7 at.% Aluminium a turning point in twinning activity was noticed and a further increase in Aluminium did result in a dramatic loss of twinning activity particularly when the material had been exposed to an additional low temperature age. The dramatic decrease of twinning activity is strongly correlated with increasing evidence of short range ordering and also early signs of Ti3Al-formation in case of the highest Aluminium content. In addition, electron backscatter diffraction analysis revealed that the formation of Aluminium ordered zones do severely hinder growth of twin boundaries

Development and potential role of type-2 sodium-glucose transporter inhibitors for management of type 2 diabetes

There is a recognized need for new treatment options for type 2 diabetes mellitus (T2DM). Recovery of glucose from the glomerular filtrate represents an important mechanism in maintaining glucose homeostasis and represents a novel target for the management of T2DM. Recovery of glucose from the glomerular filtrate is executed principally by the type 2 sodium-glucose cotransporter (SGLT2). Inhibition of SGLT2 promotes glucose excretion and normalizes glycemia in animal models. First reports of specifically designed SGLT2 inhibitors began to appear in the second half of the 1990s. Several candidate SGLT2 inhibitors are currently under development, with four in the later stages of clinical testing. The safety profile of SGLT2 inhibitors is expected to be good, as their target is a highly specific membrane transporter expressed almost exclusively within the renal tubules. One safety concern is that of glycosuria, which could predispose patients to increased urinary tract infections. So far the reported safety profile of SGLT2 inhibitors in clinical studies appears to confirm that the class is well tolerated. Where SGLT2 inhibitors will fit in the current cascade of treatments for T2DM has yet to be established. The expected favorable safety profile and insulin-independent mechanism of action appear to support their use in combination with other antidiabetic drugs. Promotion of glucose excretion introduces the opportunity to clear calories (80–90 g [300–400 calories] of glucose per day) in patients that are generally overweight, and is expected to work synergistically with weight reduction programs. Experience will most likely lead to better understanding of which patients are likely to respond best to SGLT2 inhibitors, and under what circumstances

Novel genetic loci associated with hippocampal volume

The hippocampal formation is a brain structure integrally involved in episodic memory, spatial navigation, cognition and stress responsiveness. Structural abnormalities in hippocampal volume and shape are found in several common neuropsychiatric disorders. To identify the genetic underpinnings of hippocampal structure here we perform a genome-wide association study (GWAS) of 33,536 individuals and discover six independent loci significantly associated with hippocampal volume, four of them novel. Of the novel loci, three lie within genes (ASTN2, DPP4 and MAST4) and one is found 200 kb upstream of SHH. A hippocampal subfield analysis shows that a locus within the MSRB3 gene shows evidence of a localized effect along the dentate gyrus, subiculum, CA1 and fissure. Further, we show that genetic variants associated with decreased hippocampal volume are also associated with increased risk for Alzheimer's disease (rg =-0.155). Our findings suggest novel biological pathways through which human genetic variation influences hippocampal volume and risk for neuropsychiatric illness