463 research outputs found
Reply to Comment on "Pulsar velocities and neutrino oscillations"
We have recently proposed an explanation for the birth velocities of pulsars
based on neutrino oscillations (hep-ph/9606428). One of the quantities, dN/dT,
was evaluated in the approximation of constant chemical potential for the
electrons. An alternative approximation based on the assumption Ye=const, used
by Qian (astro-ph/9705055), yields a somewhat higher prediction for the
magnetic field inside a neutron star. If the same input parameters are used,
the two approximations are in reasonable agreement, given the uncertainty in
the geometry of the magnetic field and the simplified picture of neutrino
emission that comes with the notion of a neutrinosphere.Comment: 2 pages, no figure
Exact Free Energy Functional for a Driven Diffusive Open Stationary Nonequilibrium System
We obtain the exact probability of finding a
macroscopic density profile in the stationary nonequilibrium state of
an open driven diffusive system, when the size of the system .
, which plays the role of a nonequilibrium free energy, has a very
different structure from that found in the purely diffusive case. As there,
is nonlocal, but the shocks and dynamic phase transitions of the
driven system are reflected in non-convexity of , in discontinuities in
its second derivatives, and in non-Gaussian fluctuations in the steady state.Comment: LaTeX2e, RevTeX4, PiCTeX. Four pages, one PiCTeX figure included in
TeX source fil
Re-Examination of Generation of Baryon and Lepton Number Asymmetries by Heavy Particle Decay
It is shown that wave function renormalization can introduce an important
contribution to the generation of baryon and lepton number asymmetries by heavy
particle decay. These terms, omitted in previous analyses, are of the same
order of magnitude as the standard terms. A complete cancellation of leading
terms can result in some interesting cases.Comment: 12 pages, 2 Feynman graphs (not included), UPR-055
A proposed experimental method to determine -sensitivity of splitting between ground and 7.6 eV isomeric states in Th-229
The 7.6 eV electromagnetic transition between the nearly degenerate ground
state and first excited state in the Th-229 nucleus may be very sensitive to
potential changes in the fine-structure constant, .
However, the sensitivity is not known, and nuclear calculations are currently
unable to determine it. We propose measurements of the differences of atomic
transition frequencies between thorium atoms (or ions) with the nucleus in the
ground state and in the first excited (isomeric) state. This will enable
extraction of the change in nuclear charge radius and electric quadrupole
moment between the isomers, and hence the -dependence of the isomeric
transition frequency with reasonable accuracy.Comment: More details, some changes to notatio
TIE1 and TEK signalling, intraocular pressure, and primary open-angle glaucoma: a Mendelian randomization study
Background: In primary open-angle glaucoma (POAG), lowering intraocular pressure (IOP) is the only proven way of slowing vision loss. Schlemm’s canal (SC) is a hybrid vascular and lymphatic vessel that mediates aqueous humour drainage from the anterior ocular chamber. Animal studies support the importance of SC endothelial angiopoietin-TEK signalling, and more recently TIE1 signalling, in maintaining normal IOP. However, human genetic support for a causal role of TIE1 and TEK signalling in lowering IOP is currently lacking. Methods: GWAS summary statistics were obtained for plasma soluble TIE1 (sTIE1) protein levels (N = 35,559), soluble TEK (sTEK) protein levels (N = 35,559), IOP (N = 139,555) and POAG (Ncases = 16,677, Ncontrols = 199,580). Mendelian randomization (MR) was performed to estimate the association of genetically proxied TIE1 and TEK protein levels with IOP and POAG liability. Where significant MR estimates were obtained, genetic colocalization was performed to assess the probability of a shared causal variant (PPshared) versus distinct (PPdistinct) causal variants underlying TIE1/TEK signalling and the outcome. Publicly available single-nucleus RNA-sequencing data were leveraged to investigate differential expression of TIE1 and TEK in the human ocular anterior segment. Results: Increased genetically proxied TIE1 signalling and TEK signalling associated with a reduction in IOP (− 0.21 mmHg per SD increase in sTIE1, 95% CI = − 0.09 to − 0.33 mmHg, P = 6.57 × 10–4, and − 0.14 mmHg per SD decrease in sTEK, 95% CI = − 0.03 to − 0.25 mmHg, P = 0.011), but not with POAG liability. Colocalization analysis found that the probability of a shared causal variant was greater for TIE1 and IOP than for TEK and IOP (PPshared/(PPdistinct + PPshared) = 0.98 for TIE1 and 0.30 for TEK). In the anterior segment, TIE1 and TEK were preferentially expressed in SC, lymphatic, and vascular endothelium. Conclusions: This study provides novel human genetic support for a causal role of both TIE1 and TEK signalling in regulating IOP. Here, combined evidence from cis-MR and colocalization analyses provide stronger support for TIE1 than TEK as a potential IOP-lowering therapeutic target
TIE1 and TEK signalling, intraocular pressure, and primary open-angle glaucoma: a Mendelian randomization study
BACKGROUND: In primary open-angle glaucoma (POAG), lowering intraocular pressure (IOP) is the only proven way of slowing vision loss. Schlemm's canal (SC) is a hybrid vascular and lymphatic vessel that mediates aqueous humour drainage from the anterior ocular chamber. Animal studies support the importance of SC endothelial angiopoietin-TEK signalling, and more recently TIE1 signalling, in maintaining normal IOP. However, human genetic support for a causal role of TIE1 and TEK signalling in lowering IOP is currently lacking. METHODS: GWAS summary statistics were obtained for plasma soluble TIE1 (sTIE1) protein levels (N = 35,559), soluble TEK (sTEK) protein levels (N = 35,559), IOP (N = 139,555) and POAG (Ncases = 16,677, Ncontrols = 199,580). Mendelian randomization (MR) was performed to estimate the association of genetically proxied TIE1 and TEK protein levels with IOP and POAG liability. Where significant MR estimates were obtained, genetic colocalization was performed to assess the probability of a shared causal variant (PPshared) versus distinct (PPdistinct) causal variants underlying TIE1/TEK signalling and the outcome. Publicly available single-nucleus RNA-sequencing data were leveraged to investigate differential expression of TIE1 and TEK in the human ocular anterior segment. RESULTS: Increased genetically proxied TIE1 signalling and TEK signalling associated with a reduction in IOP (- 0.21 mmHg per SD increase in sTIE1, 95% CI = - 0.09 to - 0.33 mmHg, P = 6.57 × 10-4, and - 0.14 mmHg per SD decrease in sTEK, 95% CI = - 0.03 to - 0.25 mmHg, P = 0.011), but not with POAG liability. Colocalization analysis found that the probability of a shared causal variant was greater for TIE1 and IOP than for TEK and IOP (PPshared/(PPdistinct + PPshared) = 0.98 for TIE1 and 0.30 for TEK). In the anterior segment, TIE1 and TEK were preferentially expressed in SC, lymphatic, and vascular endothelium. CONCLUSIONS: This study provides novel human genetic support for a causal role of both TIE1 and TEK signalling in regulating IOP. Here, combined evidence from cis-MR and colocalization analyses provide stronger support for TIE1 than TEK as a potential IOP-lowering therapeutic target
Majorana and the quasi-stationary states in Nuclear Physics
A complete theoretical model describing artificial disintegration of nuclei
by bombardment with alpha-particles, developed by Majorana as early as in 1930,
is discussed in detail alongside the basic experimental evidences that
motivated it. By following the quantum dynamics of a state resulting from the
superposition of a discrete state with a continuum one, whose interaction is
described by a given potential term, Majorana obtained (among the other
predictions) the explicit expression for the integrated cross section of the
nuclear process, which is the direct measurable quantity of interest in the
experiments. Though this is the first application of the concept of
quasi-stationary states to a Nuclear Physics problem, it seems also that the
unpublished Majorana's work anticipates by several years the related seminal
paper by Fano on Atomic Physics.Comment: latex, amsart, 13 page
Dynamics of fluctuations in a fluid below the onset of Rayleigh-B\'enard convection
We present experimental data and their theoretical interpretation for the
decay rates of temperature fluctuations in a thin layer of a fluid heated from
below and confined between parallel horizontal plates. The measurements were
made with the mean temperature of the layer corresponding to the critical
isochore of sulfur hexafluoride above but near the critical point where
fluctuations are exceptionally strong. They cover a wide range of temperature
gradients below the onset of Rayleigh-B\'enard convection, and span wave
numbers on both sides of the critical value for this onset. The decay rates
were determined from experimental shadowgraph images of the fluctuations at
several camera exposure times. We present a theoretical expression for an
exposure-time-dependent structure factor which is needed for the data analysis.
As the onset of convection is approached, the data reveal the critical
slowing-down associated with the bifurcation. Theoretical predictions for the
decay rates as a function of the wave number and temperature gradient are
presented and compared with the experimental data. Quantitative agreement is
obtained if allowance is made for some uncertainty in the small spacing between
the plates, and when an empirical estimate is employed for the influence of
symmetric deviations from the Oberbeck-Boussinesq approximation which are to be
expected in a fluid with its density at the mean temperature located on the
critical isochore.Comment: 13 pages, 10 figures, 52 reference
Screened and Unscreened Phases in Sedimenting Suspensions
A coarse-grained stochastic hydrodynamical description of velocity and
concentration fluctuations in steadily sedimenting suspensions is constructed,
and analyzed using self-consistent and renormalization group methods. We find
that there exists a dynamical, non-equilibrium phase transition from an
"unscreened" phase in which we recover the Caflisch-Luke (R.E. Caflisch and
J.H.C. Luke, Phys. Fluids 28, 759 (1985)) divergence of the velocity variance
to a "screened" phase where the velocity fluctuations have a finite correlation
length growing as where is the particle volume fraction,
in agreement with Segr\`e et. al. (Phys. Rev. Lett. 79, 2574 (1997)) and the
velocity variance is independent of system size. Detailed predictions are made
for the correlation function in both phases and at the transition.Comment: 4 pages, revtex 1 figur
Signatures of arithmetic simplicity in metabolic network architecture
Metabolic networks perform some of the most fundamental functions in living
cells, including energy transduction and building block biosynthesis. While
these are the best characterized networks in living systems, understanding
their evolutionary history and complex wiring constitutes one of the most
fascinating open questions in biology, intimately related to the enigma of
life's origin itself. Is the evolution of metabolism subject to general
principles, beyond the unpredictable accumulation of multiple historical
accidents? Here we search for such principles by applying to an artificial
chemical universe some of the methodologies developed for the study of genome
scale models of cellular metabolism. In particular, we use metabolic flux
constraint-based models to exhaustively search for artificial chemistry
pathways that can optimally perform an array of elementary metabolic functions.
Despite the simplicity of the model employed, we find that the ensuing pathways
display a surprisingly rich set of properties, including the existence of
autocatalytic cycles and hierarchical modules, the appearance of universally
preferable metabolites and reactions, and a logarithmic trend of pathway length
as a function of input/output molecule size. Some of these properties can be
derived analytically, borrowing methods previously used in cryptography. In
addition, by mapping biochemical networks onto a simplified carbon atom
reaction backbone, we find that several of the properties predicted by the
artificial chemistry model hold for real metabolic networks. These findings
suggest that optimality principles and arithmetic simplicity might lie beneath
some aspects of biochemical complexity
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