Consistent supersymmetric Kaluza--Klein truncations with massive modes

We construct consistent Kaluza--Klein reductions of D=11 supergravity to four dimensions using an arbitrary seven-dimensional Sasaki--Einstein manifold. At the level of bosonic fields, we extend the known reduction, which leads to minimal N=2 gauged supergravity, to also include a multiplet of massive fields, containing the breathing mode of the Sasaki--Einstein space, and still consistent with N=2 supersymmetry. In the context of flux compactifications, the Sasaki--Einstein reductions are generalizations of type IIA SU(3)-structure reductions which include both metric and form-field flux and lead to a massive universal tensor multiplet. We carry out a similar analysis for an arbitrary weak G_2 manifold leading to an N=1 supergravity with massive fields. The straightforward extension of our results to the case of the seven-sphere would imply that there is a four-dimensional Lagrangian with N=8 supersymmetry containing both massless and massive spin two fields. We use our results to construct solutions of M-theory with non-relativistic conformal symmetry.Comment: 33 pages. v2: Added section on skew-whiffed solutions and some brief comments on holographic superconductors. v3: typos corrected, version to be published in JHE

Asymptotics of the Farey Fraction Spin Chain Free Energy at the Critical Point

We consider the Farey fraction spin chain in an external field $h$. Using ideas from dynamical systems and functional analysis, we show that the free energy $f$ in the vicinity of the second-order phase transition is given, exactly, by $$f \sim \frac t{\log t}-\frac1{2} \frac{h^2}t \quad \text{for} \quad h^2\ll t \ll 1 .$$ Here $t=\lambda_{G}\log(2)(1-\frac{\beta}{\beta_c})$ is a reduced temperature, so that the deviation from the critical point is scaled by the Lyapunov exponent of the Gauss map, $\lambda_G$. It follows that $\lambda_G$ determines the amplitude of both the specific heat and susceptibility singularities. To our knowledge, there is only one other microscopically defined interacting model for which the free energy near a phase transition is known as a function of two variables. Our results confirm what was found previously with a cluster approximation, and show that a clustering mechanism is in fact responsible for the transition. However, the results disagree in part with a renormalisation group treatment

The 21 cm Signature of Cosmic String Wakes

We discuss the signature of a cosmic string wake in 21cm redshift surveys. Since 21cm surveys probe higher redshifts than optical large-scale structure surveys, the signatures of cosmic strings are more manifest in 21cm maps than they are in optical galaxy surveys. We find that, provided the tension of the cosmic string exceeds a critical value (which depends on both the redshift when the string wake is created and the redshift of observation), a cosmic string wake will generate an emission signal with a brightness temperature which approaches a limiting value which at a redshift of $z + 1 = 30$ is close to 400 mK in the limit of large string tension. The signal will have a specific signature in position space: the excess 21cm radiation will be confined to a wedge-shaped region whose tip corresponds to the position of the string, whose planar dimensions are set by the planar dimensions of the string wake, and whose thickness (in redshift direction) depends on the string tension. For wakes created at $z_i + 1 = 10^3$, then at a redshift of $z + 1 = 30$ the critical value of the string tension $\mu$ is $G \mu = 6 \times 10^{-7}$, and it decreases linearly with redshift (for wakes created at the time of equal matter and radiation, the critical value is a factor of two lower at the same redshift). For smaller tensions, cosmic strings lead to an observable absorption signal with the same wedge geometry.Comment: 11 pages, 4 figures; a couple of comments added in the discussion sectio

Structure and Stability of an Amorphous Metal

Using molecular dynamics simulations, with a realistic many-body embedded-atom potential, and a novel method to characterize local order, we study the structure of pure nickel during the rapid quench of the liquid and in the resulting glass. In contrast with previous simulations with pair potentials, we find more crystalline order and fewer icosahedra for slower quenching rates, resulting in a glass less stable against crystallization. It is shown that there is not a specific amorphous structure, only the arrest of the transition from liquid to crystal, resulting in small crystalline clusters immersed in an amorphous matrix with the same structure of the liquid.Comment: 4 pages, 4 ps figs., to appear in Phys. Rev. Let

NG2 antigen is a therapeutic target for MLL-rearranged B-cell acute lymphoblastic leukemia

Altres ajuts: This work has been supported by the Asociación Española Contra el Cáncer (AECC), Beca FERO, and OM are supported by postdoctoral fellowships from the AECC scientific foundation and the Catalunya Government (Beatriu de Pinos, BP00048), respectively. PM also acknowledges the financial support from the Obra Social La Caixa-Fundaciò Josep Carreras and "Premio Miguelín".B cell acute lymphoblastic leukemia (B-ALL) is the most common childhood cancer, with cure rates of ∼80%. MLL-rearranged (MLLr) B-ALL (MLLr-B-ALL) has, however, an unfavorable prognosis with common therapy refractoriness and early relapse, and therefore new therapeutic targets are needed for relapsed/refractory MLLr-B-ALL. MLLr leukemias are characterized by the specific expression of chondroitin sulfate proteoglycan-4, also known as neuron-glial antigen-2 (NG2). NG2 was recently shown involved in leukemia invasiveness and central nervous system infiltration in MLLr-B-ALL, and correlated with lower event-free survival (EFS). We here hypothesized that blocking NG2 may synergize with established induction therapy for B-ALL based on vincristine, glucocorticoids, and l-asparaginase (VxL). Using robust patient-derived xenograft (PDX) models, we found that NG2 is crucial for MLLr-B-ALL engraftment upon intravenous (i.v.) transplantation. In vivo blockade of NG2 using either chondroitinase-ABC or an anti-NG2-specific monoclonal antibody (MoAb) resulted in a significant mobilization of MLLr-B-ALL blasts from bone marrow (BM) to peripheral blood (PB) as demonstrated by cytometric and 3D confocal imaging analysis. When combined with either NG2 antagonist, VxL treatment achieved higher rates of complete remission, and consequently higher EFS and delayed time to relapse. Mechanistically, anti-NG2 MoAb induces neither antibody-dependent cell-mediated not complement-dependent cytotoxicity. NG2 blockade rather overrides BM stroma-mediated chemoprotection through PB mobilization of MLLr-B-ALL blasts, thus becoming more accessible to chemotherapy. We provide a proof of concept for NG2 as a therapeutic target for MLLr-B-ALL

Out-of-focus Blur: Image De-blurring

Image de-blurring is important in many cases of imaging a real scene or object by a camera. This project focuses on de-blurring an image distorted by an out-of-focus blur through a simulation study. A pseudo-inverse filter is first explored but it fails because of severe noise amplification. Then Tikhonov regularization methods are employed, which produce greatly improved results compared to the pseudo-inverse filter. In Tikhonov regularization, the choice of the regularization parameter plays a critical rule in obtaining a high-quality image, and the regularized solutions possess a semi-convergence property. The best result, with the relative restoration error of 8.49%, is achieved when the prescribed discrepancy principle is used to decide an optimal value. Furthermore, an iterative method, Conjugated Gradient, is employed for image de-blurring, which is fast in computation and leads to an even better result with the relative restoration error of 8.22%. The number of iteration in CG acts as a regularization parameter, and the iterates have a semi-convergence property as well.Comment: 11 page

s-Process Nucleosynthesis in AGB Stars: A Test for Stellar Evolution

[abridged] We study the s-process in AGB stars using three different stellar evolutionary models computed for a 3Msun and solar metallicity star. First we investigate the formation and the efficiency of the main neutron source. We parametrically vary the number of protons mixed from the envelope into the C12 rich core. For p/C12 > 0.3, mainly N14 is produced, which represent a major neutron poison. The amount of C12 in the He intershell and the maximum value of the time-integrated neutron flux are proportional. Then we generate detailed s-process calculations on the basis of stellar evolutionary models constructed with three different codes. One code considers convective hydrodynamic overshoot that depends on a free parameter f, and results in partial mixing beyond convective boundaries, the most efficient third dredge up and the formation of the C13 pocket. For the other two codes an identical C13 pocket is introduced in the post-processing nucleosynthesis calculations. The models generally reproduce the spectroscopically observed s-process enhancements. The results of the cases without overshoot are remarkably similar. The code including hydrodynamic overshoot produces a He intershell composition near to that observed in H-deficient central stars of planetary nebulae. As a result of this intershell dredge up the neutron fluxes have a higher efficiency, both during the interpulse periods and within thermal pulses. The s-element distribution is pushed toward the heavier s-process elements and large abundances of neutron-rich isotopes fed by branching points in the s-process path are produced. Several observational constraints are better matched by the models without overshoot. Our study need to be extended to different masses and metallicities and in the space of the free overshoot parameter f.Comment: 44 pages, incl 10 figures, accepted for publication in Ap

Stress detection using wearable physiological and sociometric sensors

Stress remains a significant social problem for individuals in modern societies. This paper presents a machine learning approach for the automatic detection of stress of people in a social situation by combining two sensor systems that capture physiological and social responses. We compare the performance using different classifiers including support vector machine, AdaBoost, and k-nearest neighbour. Our experimental results show that by combining the measurements from both sensor systems, we could accurately discriminate between stressful and neutral situations during a controlled Trier social stress test (TSST). Moreover, this paper assesses the discriminative ability of each sensor modality individually and considers their suitability for real time stress detection. Finally, we present an study of the most discriminative features for stress detection

Sialic Acid Glycobiology Unveils Trypanosoma cruzi Trypomastigote Membrane Physiology.

Trypanosoma cruzi, the flagellate protozoan agent of Chagas disease or American trypanosomiasis, is unable to synthesize sialic acids de novo. Mucins and trans-sialidase (TS) are substrate and enzyme, respectively, of the glycobiological system that scavenges sialic acid from the host in a crucial interplay for T. cruzi life cycle. The acquisition of the sialyl residue allows the parasite to avoid lysis by serum factors and to interact with the host cell. A major drawback to studying the sialylation kinetics and turnover of the trypomastigote glycoconjugates is the difficulty to identify and follow the recently acquired sialyl residues. To tackle this issue, we followed an unnatural sugar approach as bioorthogonal chemical reporters, where the use of azidosialyl residues allowed identifying the acquired sugar. Advanced microscopy techniques, together with biochemical methods, were used to study the trypomastigote membrane from its glycobiological perspective. Main sialyl acceptors were identified as mucins by biochemical procedures and protein markers. Together with determining their shedding and turnover rates, we also report that several membrane proteins, including TS and its substrates, both glycosylphosphatidylinositol-anchored proteins, are separately distributed on parasite surface and contained in different and highly stable membrane microdomains. Notably, labeling for α(1,3)Galactosyl residues only partially colocalize with sialylated mucins, indicating that two species of glycosylated mucins do exist, which are segregated at the parasite surface. Moreover, sialylated mucins were included in lipid-raft-domains, whereas TS molecules are not. The location of the surface-anchored TS resulted too far off as to be capable to sialylate mucins, a role played by the shed TS instead. Phosphatidylinositol-phospholipase-C activity is actually not present in trypomastigotes. Therefore, shedding of TS occurs via microvesicles instead of as a fully soluble form

The yeast P5 type ATPase, Spf1, regulates manganese transport into the endoplasmic reticulum

The endoplasmic reticulum (ER) is a large, multifunctional and essential organelle. Despite intense research, the function of more than a third of ER proteins remains unknown even in the well-studied model organism Saccharomyces cerevisiae. One such protein is Spf1, which is a highly conserved, ER localized, putative P-type ATPase. Deletion of SPF1 causes a wide variety of phenotypes including severe ER stress suggesting that this protein is essential for the normal function of the ER. The closest homologue of Spf1 is the vacuolar P-type ATPase Ypk9 that influences Mn2+ homeostasis. However in vitro reconstitution assays with Spf1 have not yielded insight into its transport specificity. Here we took an in vivo approach to detect the direct and indirect effects of deleting SPF1. We found a specific reduction in the luminal concentration of Mn2+ in ∆spf1 cells and an increase following it’s overexpression. In agreement with the observed loss of luminal Mn2+ we could observe concurrent reduction in many Mn2+-related process in the ER lumen. Conversely, cytosolic Mn2+-dependent processes were increased. Together, these data support a role for Spf1p in Mn2+ transport in the cell. We also demonstrate that the human sequence homologue, ATP13A1, is a functionally conserved orthologue. Since ATP13A1 is highly expressed in developing neuronal tissues and in the brain, this should help in the study of Mn2+-dependent neurological disorders