110 research outputs found

    Reshaping-induced spatiotemporal chaos in driven, damped sine-Gordon systems

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    Spatiotemporal chaos arising from the competition between sine-Gordon-breather and kink-antikink-pair solitons by reshaping an ac force is demonstrated. After introducing soliton collective coordinates, Melnikov's method is applied to the resulting effective equation of motion to estimate the parameter-space regions of the ac force where homoclinic bifurcations are induced. The analysis reveals that the chaos-order threshold exhibits sensitivity to small changes in the force shape. Computer simulations of the sine-Gordon system show good agreement with these theoretical predictions.Comment: 11 pages, 3 figure

    Nonlinear plasmonic slot waveguides

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    We study nonlinear modes in subwavelength slot waveguides created by a nonlinear dielectric slab sandwiched between two metals. We present the dispersion diagrams of the families of nonlinear plasmonic modes and reveal that the symmetric mode undergoes the symmetry-breaking bifurcation with the energy primarily localized near one of the interfaces. We also find that the antisymmetric mode may split into two brunches giving birth to two families of nonlinear antisymmetric modes.Comment: 6 pages, 5 figure

    Dynamical phase diagram of the dc-driven underdamped Frenkel-Kontorova chain

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    Multistep dynamical phase transition from the locked to the running state of atoms in response to a dc external force is studied by MD simulations of the generalized Frenkel-Kontorova model in the underdamped limit. We show that the hierarchy of transition recently reported [Braun et al, Phys. Rev. Lett. 78, 1295 (1997)] strongly depends on the value of the friction constant. A simple phenomenological explanation for the friction dependence of the various critical forces separating intermediate regimes is given.Comment: 12 Revtex Pages, 4 EPS figure

    On the derivative of the associated Legendre function of the first kind of integer order with respect to its degree

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    In our recent works [R. Szmytkowski, J. Phys. A 39 (2006) 15147; corrigendum: 40 (2007) 7819; addendum: 40 (2007) 14887], we have investigated the derivative of the Legendre function of the first kind, Pν(z)P_{\nu}(z), with respect to its degree ν\nu. In the present work, we extend these studies and construct several representations of the derivative of the associated Legendre function of the first kind, Pν±m(z)P_{\nu}^{\pm m}(z), with respect to the degree ν\nu, for mNm\in\mathbb{N}. At first, we establish several contour-integral representations of Pν±m(z)/ν\partial P_{\nu}^{\pm m}(z)/\partial\nu. They are then used to derive Rodrigues-type formulas for [Pν±m(z)/ν]ν=n[\partial P_{\nu}^{\pm m}(z)/\partial\nu]_{\nu=n} with nNn\in\mathbb{N}. Next, some closed-form expressions for [Pν±m(z)/ν]ν=n[\partial P_{\nu}^{\pm m}(z)/\partial\nu]_{\nu=n} are obtained. These results are applied to find several representations, both explicit and of the Rodrigues type, for the associated Legendre function of the second kind of integer degree and order, Qn±m(z)Q_{n}^{\pm m}(z); the explicit representations are suitable for use for numerical purposes in various regions of the complex zz-plane. Finally, the derivatives [2Pνm(z)/ν2]ν=n[\partial^{2}P_{\nu}^{m}(z)/\partial\nu^{2}]_{\nu=n}, [Qνm(z)/ν]ν=n[\partial Q_{\nu}^{m}(z)/\partial\nu]_{\nu=n} and [Qνm(z)/ν]ν=n1[\partial Q_{\nu}^{m}(z)/\partial\nu]_{\nu=-n-1}, all with m>nm>n, are evaluated in terms of [Pνm(±z)/ν]ν=n[\partial P_{\nu}^{-m}(\pm z)/\partial\nu]_{\nu=n}.Comment: LateX, 40 pages, 1 figure, extensive referencin

    Appetite and gut hormone responses to moderate-intensity continuous exercise versus high-intensity interval exercise, in normoxic and hypoxic conditions.

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    This study investigated the effects of continuous moderate-intensity exercise (MIE) and high-intensity interval exercise (HIIE) in combination with short exposure to hypoxia on appetite and plasma concentrations of acylated ghrelin, peptide YY (PYY), and glucagon-like peptide-1 (GLP-1). Twelve healthy males completed four, 2.6 h trials in a random order: 1) MIE-normoxia, 2) MIE-hypoxia, 3) HIIE-normoxia, and 4) HIIE-hypoxia. Exercise took place in an environmental chamber. During MIE, participants ran for 50 min at 70% of altitude-specific maximal oxygen uptake ( 2max) and during HIIE performed 6 x 3 min running at 90% 2max interspersed with 6 x 3 min active recovery at 50% 2max with a 7 min warm-up and cool-down at 70% 2max (50 min total). In hypoxic trials, exercise was performed at a simulated altitude of 2,980 m (14.5% O2). Exercise was completed after a standardised breakfast. A second meal standardised to 30% of participants’ daily energy requirements was provided 45 min after exercise. Appetite was suppressed more in hypoxia than normoxia during exercise, post-exercise, and for the full 2.6 h trial period (linear mixed modelling, p 0.05). These findings demonstrate that short exposure to hypoxia causes suppressions in appetite and plasma acylated ghrelin concentrations. Furthermore, appetite responses to exercise do not appear to be influenced by exercise modality

    Unacylated ghrelin promotes adipogenesis in rodent bone marrow via ghrelin O-acyl transferase and GHS-R1a activity: evidence for target cell-induced acylation

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    Despite being unable to activate the cognate ghrelin receptor (GHS-R), unacylated ghrelin (UAG) possesses a unique activity spectrum that includes promoting bone marrow adipogenesis. Since a receptor mediating this action has not been identified, we re-appraised the potential interaction of UAG with GHS-R in the regulation of bone marrow adiposity. Surprisingly, the adipogenic effects of intra-bone marrow (ibm)-infused acylated ghrelin (AG) and UAG were abolished in male GHS-R-null mice. Gas chromatography showed that isolated tibial marrow adipocytes contain the medium-chain fatty acids utilised in the acylation of UAG, including octanoic acid. Additionally, immunohistochemistry and immunogold electron microscopy revealed that tibial marrow adipocytes show prominent expression of the UAG-activating enzyme ghrelin O-acyl transferase (GOAT), which is located in the membranes of lipid trafficking vesicles and in the plasma membrane. Finally, the adipogenic effect of ibm-infused UAG was completely abolished in GOAT-KO mice. Thus, the adipogenic action of exogenous UAG in tibial marrow is dependent upon acylation by GOAT and activation of GHS-R. This suggests that UAG is subject to target cell-mediated activation – a novel mechanism for manipulating hormone activity
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