2,536 research outputs found
The randomly driven Ising ferromagnet, Part II: One and two dimensions
We consider the behavior of an Ising ferromagnet obeying the Glauber dynamics
under the influence of a fast switching, random external field. In Part I, we
introduced a general formalism for describing such systems and presented the
mean field theory. In this article we derive results for the one dimensional
case, which can be only partially solved. Monte Carlo simulations performed on
a square lattice indicate that the main features of the mean field theory
survive the presence of strong fluctuations.Comment: 10 pages in REVTeX/LaTeX format, 17 eps/ps figures. Submitted to
Journal of Physics
The randomly driven Ising ferromagnet, Part I: General formalism and mean field theory
We consider the behavior of an Ising ferromagnet obeying the Glauber dynamics
under the influence of a fast switching, random external field. After
introducing a general formalism for describing such systems, we consider here
the mean-field theory. A novel type of first order phase transition related to
spontaneous symmetry breaking and dynamic freezing is found. The
non-equilibrium stationary state has a complex structure, which changes as a
function of parameters from a singular-continuous distribution with Euclidean
or fractal support to an absolutely continuous one.Comment: 12 pages REVTeX/LaTeX format, 12 eps/ps figures. Submitted to Journal
of Physics
Temporally disordered Ising models
We present a study of the influence of different types of disorder on systems
in the Ising universality class by employing both a dynamical field theory
approach and extensive Monte Carlo simulations. We reproduce some well known
results for the case of quenched disorder (random temperature and random
field), and analyze the effect of four different types of time-dependent
disorder scarcely studied so far in the literature. Some of them are of obvious
experimental and theoretical relevance (as for example, globally fluctuating
temperatures or random fields). All the predictions coming from our field
theoretical analysis are fully confirmed by extensive simulations in two and
three dimensions, and novel qualitatively different, non-Ising transitions are
reported. Possible experimental setups designed to explore the described
phenomenologies are also briefly discussed.Comment: Submitted to Phys. Rev. E. Rapid Comm. 4 page
Moduli spaces of toric manifolds
We construct a distance on the moduli space of symplectic toric manifolds of
dimension four. Then we study some basic topological properties of this space,
in particular, path-connectedness, compactness, and completeness. The
construction of the distance is related to the Duistermaat-Heckman measure and
the Hausdorff metric. While the moduli space, its topology and metric, may be
constructed in any dimension, the tools we use in the proofs are
four-dimensional, and hence so is our main result.Comment: To appear in Geometriae Dedicata, minor changes to previous version,
19 pages, 6 figure
Single Color Centers Implanted in Diamond Nanostructures
The development of materials processing techniques for optical diamond
nanostructures containing a single color center is an important problem in
quantum science and technology. In this work, we present the combination of ion
implantation and top-down diamond nanofabrication in two scenarios: diamond
nanopillars and diamond nanowires. The first device consists of a 'shallow'
implant (~20nm) to generate Nitrogen-vacancy (NV) color centers near the top
surface of the diamond crystal. Individual NV centers are then isolated
mechanically by dry etching a regular array of nanopillars in the diamond
surface. Photon anti-bunching measurements indicate that a high yield (>10%) of
the devices contain a single NV center. The second device demonstrates 'deep'
(~1\mu m) implantation of individual NV centers into pre-fabricated diamond
nanowire. The high single photon flux of the nanowire geometry, combined with
the low background fluorescence of the ultrapure diamond, allows us to sustain
strong photon anti-bunching even at high pump powers.Comment: 20 pages, 7 figure
The Dynamics of Nestedness Predicts the Evolution of Industrial Ecosystems
In economic systems, the mix of products that countries make or export has
been shown to be a strong leading indicator of economic growth. Hence, methods
to characterize and predict the structure of the network connecting countries
to the products that they export are relevant for understanding the dynamics of
economic development. Here we study the presence and absence of industries at
the global and national levels and show that these networks are significantly
nested. This means that the less filled rows and columns of these networks'
adjacency matrices tend to be subsets of the fuller rows and columns. Moreover,
we show that nestedness remains relatively stable as the matrices become more
filled over time and that this occurs because of a bias for industries that
deviate from the networks' nestedness to disappear, and a bias for the missing
industries that reduce nestedness to appear. This makes the appearance and
disappearance of individual industries in each location predictable. We
interpret the high level of nestedness observed in these networks in the
context of the neutral model of development introduced by Hidalgo and Hausmann
(2009). We show that, for the observed fills, the model can reproduce the high
level of nestedness observed in these networks only when we assume a high level
of heterogeneity in the distribution of capabilities available in countries and
required by products. In the context of the neutral model, this implies that
the high level of nestedness observed in these economic networks emerges as a
combination of both, the complementarity of inputs and heterogeneity in the
number of capabilities available in countries and required by products. The
stability of nestedness in industrial ecosystems, and the predictability
implied by it, demonstrates the importance of the study of network properties
in the evolution of economic networks.Comment: 26 page
Kontrola kvalitete pri biosintezi aminoacil-tRNA
The fidelity of translation is determined at two major points: the accuracy of aminoacyl-tRNA selection by the ribosomes and synthesis of cognate amino acid/tRNA pairs by aminoacyl-tRNA synthetases (aaRSs) in the course of the aminoacylation reaction. The most important point in aminoacylation is the accurate recognition of cognate substrates coupled with discrimination of
non-cognates. While this is generally accomplished by a single enzyme, we have recently found that discrimination against lysine analogues requires the existence of two unrelated lysyl-tRNA synthetases. For other amino acids, initial recognition is not sufficiently accurate with errors being
corrected by an intrinsic editing activity. Recent studies indicate how editing prevents the misinterpretation of phenylalanine as tyrosine in the genetic code and have shown the importance of this process in vivo. More recent studies indicate that while these editing reactions are critical in
the cytoplasm, some are absent from mitochondria suggesting that the overall fidelity of protein synthesis might be reduced in this compartment.Vjernost translacije bitno ovisi o točnosti dvaju koraka: odabiru aminoacil-tRNA na ribosomu i sintezi ispravnih aminoacil-tRNA pomoću odgovarajućih aminoacil-tRNA-sintetaza u reakciji aminoaciliranja. Najvažniji događaj u aminoaciliranju precizno je prepoznavanje pripadnih supstrata (tRNA i aminokiseline) i diskriminacija nepripadnih. Iako taj posao uglavnom obavlja po jedan enzim za svaki par tRNA : aminokiselina, nedavno smo ustanovili da su za diskriminaciju analoga lizina potrebne dvije različite lizil-tRNA-sintetaze. U nekim drugim slučajevima otkriveno je da su pogreške u odabiru tRNA i njihovih pripadnih aminokiseline i suviše velike, pa je nužan
naknadni popravak pogrešnih produkata u reakciji aminoaciliranja, koji također mogu katalizirati neke aminoacil-tRNA-sintetaze. Na primjeru krivog odabira tirozina umjesto fenilalanina, te naknadnog popravka, pokazano je kako je mogućnost korekcije važna u sprečavanju pogrešne translacije genetičkog koda in vivo. Najnovija istraživanja pokazala su da su mehanizmi popravka od ključne važnosti u citoplazmi, no neki se ne zbivaju u mitohondriju, ukazujući na smanjenu ukupnu točnost biosinteze proteina u ovom staničnom odjeljku
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