1,161 research outputs found
Proposal of a novel design for linear superconducting motor using 2G tape stacks
This paper presents a new design for a su-
perconducting linear motor (SLM). This SLM uses stacks
of second-generation (2G) superconducting tapes, which
are responsible for replacing yttrium barium copper oxide
bulks. The proposed SLM may operate as a synchronous
motor or as a hysteresis motor, depending on the load
force magnitude. A small-scale linear machine prototype
with 2G stacks was constructed and tested to investigate
the proposed SLM topology. The stator traveling magnetic
field wave was represented by several Nd-Fe-B permanent
magnets. A relative movement was produced between the
stator and the stack, and the force was measured along the
displacement. This system was also simulated by the finite
element method, in order to calculate the induced currents
in the stack and determine the electromagnetic force. The
H-formulation was used to solve the problem, and a power
law relation was applied to take into account the intrin-
sically nonlinearity of the superconductor. The simulated
and measured results were in accordance. Simulated re-
sults were extrapolated, proving to be an interesting tool to
scale up the motor in future projects. The proposed motor
presented an estimated force density of almost 500 N/kg,
which is much higher than any linear motor.This work was supported in part by the following agencies: CNPq/CAPES/INERGE, CNPq—Ci ˆ encias sem Fronteiras, FAPERJ, Catalan Government 2014- SGR-753, CONSOLIDER Excellence Network MAT2014-56063-C2-1-R and MAT2015-68994-REDC, Eurofusion EU COST ACTIONS MP1201/ MP1014/PPPT-WPMAG 2014, EUROTAPES FP7-NMP-Large-2011- 280432, FORTISSIMO FP7-2013-ICT-609029, and Spanish Govern- ment Agencies—Severo Ochoa Programme Centres of Excellence in R&D. (Corresponding author: Guilherme G. Sotelo.
Canonical and unconventional purposes and mechanisms
Selective autophagic degradation of cellular components underlies many of the important physiological and pathological implications that autophagy has for mammalian cells. Cytoplasmic vesicles, just like other intracellular items, can be subjected to conventional autophagic events where double-membrane autophagosomes specifically isolate and deliver them for lysosomal destruction. However, intracellular membranes appear to constitute common platforms for unconventional versions of the autophagic pathway, a notion that has become apparent during the past few years. For instance, in many cases of autophagy directed against bacterial phagosomes, subversion of the process results in multimembrane vacuoles that promote bacterial replication instead of the usual degradative outcome. In a different atypical modality, single-membrane vesicles can be labeled with LC3 to direct their contents for lysosomal degradation. In fact, single-membrane compartments of various kinds often provide an assembly site for the autophagic machinery to perform unanticipated nondegradative activities that range from localized secretion of lysosomal contents to melanosome function. Interestingly, many of these unconventional processes seem to be initiated through engagement of relevant nodes of the autophagic signaling network that, once activated, promote LC3 decoration of the targeted membrane, and some cases of inducer/receptor proteins that specifically engage those important signaling hubs have recently been described. Here we review the available examples of all autophagic variants involving membranous compartments, with a main focus on the more recently discovered unconventional phenomena where the usual degradation purpose of autophagy or its canonical mechanistic features are not completely conserved.Funding was provided by grants from the Ministerio de Ciencia e Innovación of the Spanish Government (Refs. SAF2008-00350 and SAF2011-23714), the Fundación Solórzano, the Junta de Castilla y León local government (Consejería de
Educación, Ref. CSI001A10-2, and Consejería de Sanidad) and the Consejo Superior de Investigaciones Científicas (CSIC; Ref. 200720I026). Additional funding comes from the FEDER program of the European Union. EB is a graduate student funded by a predoctoral fellowship from the FPU program (Ministerio de Educación, MEC, Spanish Government).Peer Reviewe
Bulk Fermi surface coexistence with Dirac surface state in BiSe: a comparison of photoemission and Shubnikov-de Haas measurements
Shubnikov de Haas (SdH) oscillations and Angle Resolved PhotoEmission
Spectroscopy (ARPES) are used to probe the Fermi surface of single crystals of
Bi2Se3. We find that SdH and ARPES probes quantitatively agree on measurements
of the effective mass and bulk band dispersion. In high carrier density
samples, the two probes also agree in the exact position of the Fermi level EF,
but for lower carrier density samples discrepancies emerge in the position of
EF. In particular, SdH reveals a bulk three-dimensional Fermi surface for
samples with carrier densities as low as 10^17cm-3. We suggest a simple
mechanism to explain these differences and discuss consequences for existing
and future transport studies of topological insulators.Comment: 5 mages, 5 figure
Interplay between excitation kinetics and reaction-center dynamics in purple bacteria
Photosynthesis is arguably the fundamental process of Life, since it enables
energy from the Sun to enter the food-chain on Earth. It is a remarkable
non-equilibrium process in which photons are converted to many-body excitations
which traverse a complex biomolecular membrane, getting captured and fueling
chemical reactions within a reaction-center in order to produce nutrients. The
precise nature of these dynamical processes -- which lie at the interface
between quantum and classical behaviour, and involve both noise and
coordination -- are still being explored. Here we focus on a striking recent
empirical finding concerning an illumination-driven transition in the
biomolecular membrane architecture of {\it Rsp. Photometricum} purple bacteria.
Using stochastic realisations to describe a hopping rate model for excitation
transfer, we show numerically and analytically that this surprising shift in
preferred architectures can be traced to the interplay between the excitation
kinetics and the reaction center dynamics. The net effect is that the bacteria
profit from efficient metabolism at low illumination intensities while using
dissipation to avoid an oversupply of energy at high illumination intensities.Comment: 21 pages, 13 figures, accepted for publication in New Journal of
Physic
Magnetized strangelets at finite temperature
The main properties of magnetized strangelets, namely, their energy per
baryon, radius and electric charge, are studied. Temperature effects are also
taken into account in order to study their stability compared to the 56Fe
isotope and non-magnetized strangelets using the liquid drop model. Massive
quarks are considered with the aim to have a more realistic description for
strangelets in the astrophysical context and the environment of heavy ion
colliders, playing also an important role in the thermodynamical quantities of
the quark gas. It is concluded that the presence of a magnetic field tends to
stabilize more the strangelets, even when temperature effects are taken into
account. Magnetized strangelets in a paired superconductor phase (magnetized
color flavor locked phase) are also discussed. It is shown that they are more
stable than ordinary magnetized strangelets for typical gap values of the order
of O(100) MeV.Comment: 10 pages, 10 figures, discussion extended, new references adde
Correction: Ordoñez, et al.; DNA methylation of enhancer elements in myeloid neoplasms: think outside the promoters? Cancers 2019, 11, 1424
The authors would like to make a correction to their published pape
IMplicit-EXplicit Formulations for Discontinuous Galerkin Non-Hydrostatic Atmospheric Models
This work presents IMplicit-EXplicit (IMEX) formulations for discontinuous
Galerkin (DG) discretizations of the compressible Euler equations governing
non-hydrostatic atmospheric flows. In particular, we show two different IMEX
formulations that not only treat the stiffness due to the governing dynamics
but also the domain discretization. We present these formulations for two
different equation sets typically employed in atmospheric modeling. For both
equation sets, efficient Schur complements are derived and the challenges and
remedies for deriving them are discussed. The performance of these IMEX
formulations of different orders are investigated on both 2D (box) and 3D
(sphere) test problems and shown to achieve their theoretical rates of
convergence and their efficiency with respect to both mesoscale and global
applications are presented
DNA methylation of enhancer elements in myeloid neoplasms: think outside the promoters?
Gene regulation through DNA methylation is a well described phenomenon that has a
prominent role in physiological and pathological cell-states. This epigenetic modification is usually
grouped in regions denominated CpG islands, which frequently co-localize with gene promoters,
silencing the transcription of those genes. Recent genome-wide DNA methylation studies have
challenged this paradigm, demonstrating that DNA methylation of regulatory regions outside
promoters is able to influence cell-type specific gene expression programs under physiologic or
pathologic conditions. Coupling genome-wide DNA methylation assays with histone mark annotation
has allowed for the identification of specific epigenomic changes that affect enhancer regulatory
regions, revealing an additional layer of complexity to the epigenetic regulation of gene expression.
In this review, we summarize the novel evidence for the molecular and biological regulation of
DNA methylation in enhancer regions and the dynamism of these changes contributing to the
fine-tuning of gene expression. We also analyze the contribution of enhancer DNA methylation on the
expression of relevant genes in acute myeloid leukemia and chronic myeloproliferative neoplasms.
The characterization of the aberrant enhancer DNA methylation provides not only a novel pathogenic
mechanism for different tumors but also highlights novel potential therapeutic targets for myeloid
derived neoplasms
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