What sets the magnetic field strength and cycle period in solar-type stars?

Two fundamental properties of stellar magnetic fields have been determined by observations for solar-like stars with different Rossby numbers (Ro), namely, the magnetic field strength and the magnetic cycle period. The field strength exhibits two regimes: 1) for fast rotation it is independent of Ro, 2) for slow rotation it decays with Ro following a power law. For the magnetic cycle period two regimes of activity, the active and inactive branches, also have been identified. For both of them, the longer the rotation period, the longer the activity cycle. Using global dynamo simulations of solar like stars with Rossby numbers between ~0.4 and ~2, this paper explores the relevance of rotational shear layers in determining these observational properties. Our results, consistent with non-linear alpha^2-Omega dynamos, show that the total magnetic field strength is independent of the rotation period. Yet at surface levels, the origin of the magnetic field is determined by Ro. While for Ro<1 it is generated in the convection zone, for Ro>1 strong toroidal fields are generated at the tachocline and rapidly emerge towards the surface. In agreement with the observations, the magnetic cycle period increases with the rotational period. However, a bifurcation is observed for Ro~1, separating a regime where oscillatory dynamos operate mainly in the convection zone, from the regime where the tachocline has a predominant role. In the latter the cycles are believed to result from the periodic energy exchange between the dynamo and the magneto-shear instabilities developing in the tachocline and the radiative interior.Comment: 43 pages, 14 figures, accepted for publication in The Astrophysical Journa

Evidence for a Very Large-Scale Fractal Structure in the Universe from Cobe Measurements

In this work, we analyse the temperature fluctuations of the cosmic microwave background radiation observed by COBE and show that the distribution can be fitted by a fractal distribution with a fractal dimension $D= 1.43 \pm 0.07$. This value is in close agreement with the fractal dimension obtained by Coleman and Pietronero (1992) and Luo and Schramm (1992) from galaxy-galaxy and cluster-cluster correlations up to $\sim 100 h^{-1} Mpc$. The fact that the observed temperature fluctuations correspond to scales much larger than $100 h^{-1} Mpc$ and are signatures of the primordial density fluctuations at the recombination layer suggests that the structure of the matter at the early universe was already fractal and thus non-homogeneous on those scales. This result may have important consequences for the theoretical framework that describes the universe.Comment: 11 pages, postscript file, 2 figures available upon request. To appear in ApJ Letter

The Coupling Mechanisms in the CO2 Laser Welding of Copper

The CO2 laser is a potentially powerful tool for welding, allowing high integrity joints to be produced with minimal thermal damage and high joint completion rates. Its use in the joining of reflective, high conductivity materials, such as copper is, however, limited. The current work examined the high power CO2 laser welding of oxygen free high conductivity copper and in particular the coupling mechanisms which appear to control the consistency of the process. The role of the plasma control jet was found to have a fundamental influence on the coupling behaviour. Due to the practical problems of direct observation of the jet gas flow during welding, the process was modelled using a flow simulation package. The results of the simulation enabled a satisfactory theory for the coupling mechanism to be developed. Plasma plume formation and maintenance during the welding process appeared to be responsible for coupling and to occur by a non-conventional mechanism. The theory explains the anomalies in previous work and indicates how the process consistency may be improved.Ph

Amino acids in the development of Prodrugs

Although drugs currently used for the various types of diseases (e.g., antiparasitic, antiviral, antibacterial, etc.) are effective, they present several undesirable pharmacological and pharmaceutical properties. Most of the drugs have low bioavailability, lack of sensitivity, and do not target only the damaged cells, thus also affecting normal cells. Moreover, there is the risk of developing resistance against drugs upon chronic treatment. Consequently, their potential clinical applications might be limited and therefore, it is mandatory to find strategies that improve those properties of therapeutic agents. The development of prodrugs using amino acids as moieties has resulted in improvements in several properties, namely increased bioavailability, decreased toxicity of the parent drug, accurate delivery to target tissues or organs, and prevention of fast metabolism. Herein, we provide an overview of models currently in use of prodrug design with amino acids. Furthermore, we review the challenges related to the permeability of poorly absorbed drugs and transport and deliver on target organs.NV acknowledges support from Fundação para a Ciência e Tecnologia (FCT, Lisbon, Portugal) and FEDER (European Union), award number IF/00092/2014/CP1255/CT0004. NV also thanks FCT for the IF position and Fundação Manuel António da Mota (FMAM, Porto, Portugal) and Pfizer (Portugal) for support for the Nuno Vale Research Group. The contents of this report are solely the responsibility of the authors and do not necessarily represent the official views of the FCT, FMAM and Pfizer

Inhibition of the formation in vitro of putatively carcinogenic metabolites derived from S. Haematobium and O. Viverrini by Combination of Drugs with Antioxidants

Infections caused by Schistosoma haematobium and Opisthorchis viverrini are classified as carcinogenic. Although carcinogenesis might be a multifactorial process, it has been postulated that these helminth produce/excrete oxysterols and estrogen-like metabolites that might act as initiators of their infection-associated carcinogenesis. Current treatment and control of these infections rely on a single drug, praziquantel, that mainly targets the parasites and not the pathologies related to the infection including cancer. Thus, there is a need to search for novel therapeutic alternatives that might include combinations of drugs and drug repurposing. Based on these concepts, we propose a novel therapeutic strategy that combines drugs with molecule antioxidants. We evaluate the efficacy of a novel therapeutic strategy to prevent the formation of putative carcinogenic metabolites precursors and DNA adducts. Firstly, we used a methodology previously established to synthesize metabolites precursors and DNA adducts in the presence of CYP450. Then, we evaluated the inhibition of their formation induced by drugs and antioxidants alone or in combination. Drugs and resveratrol alone did not show a significant inhibitory effect while N-acetylcysteine inhibited the formation of most metabolite precursors and DNA adducts. Moreover, the combinations of classical drugs with antioxidants were more effective rather than compounds alone. This strategy might be a valuable tool to prevent the initiation of helminth infection-associated carcinogenesis.This work was financed by FEDER-Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020-Operational Programme for Competitiveness and Internationalisation (POCI), Portugal 2020, and by Portuguese funds through FCT-Fundação para a Ciência e a Tecnologia, in the framework of the projects "Institute for Research and Innovation in Health Sciences" (POCI-01-0145-FEDER-007274). N.V. also acknowledges support from FCT and FEDER (European Union), award number IF/00092/2014/CP1255/CT0004. FUNDING TEXT 2: Funding: This work was financed by FEDER-Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020-Operational Programme for Competitiveness and Internationalisation (POCI), Portugal 2020, and by Portuguese funds through FCT-Fundação para a Ciência e a Tecnologia, in the framework of the projects “Institute for Research and Innovation in Health Sciences” (POCI-01-0145-FEDER-007274). N.V. also acknowledges support from FCT and FEDER (European Union), award number IF/00092/2014/CP1255/CT0004

Cumulative Effect of Cardiovascular Risk Factors on Regulation of AMPK/SIRT1-PGC-1 alpha-SIRT3 Pathway in the Human Erectile Tissue

Cardiovascular disease risk factors (CVDRF), especially diabetes mellitus (DM), disrupt oxidative stress response. This condition underlies endothelial dysfunction, early manifested in men as erectile dysfunction. The current study is aimed at elucidating the impact of CVDRF in the oxidation responsive AMPK/SIRT1-PGC-1 alpha-SIRT3 pathway and related miRNAs in the human corpus cavernosum. Human penile tissue fragments from individuals submitted to programmed urological surgeries (n=27), aged 43-63 years, were clustered depending on the presence of CVDRF; the control group included samples from patients without CVDRF, and groups A and B included samples from patients with DM and additional CVDRF, totalizing = 3 CVDRF (group B). Dual-immunolabelling of SIRT3, SOD2, or GPX1 with alpha-actin in tissue sections was carried out. The assessment of expression levels of NOX1, phospho-AMPK alpha, total AMPK alpha, SIRT1, PGC-1 alpha, SIRT3, SOD2, and GPX1 was performed by western blotting and of miR-200a, miR-34a, miR-421, and miR-206 by real-time PCR. Phospho-AMPK alpha and SIRT3 expression was found significantly increased in group B relative to other groups, suggesting a marked influence of CVDRF, additional to DM, in the regulation of these enzymes. NOX1 was also increased in group B relative to controls. Only an increasing tendency was observed in the phospho-AMPK alpha/total AMPK alpha ratio, SIRT1, and PGC-1 alpha expression in groups A and B when compared with controls. Concerning antioxidant enzymes, GPX1 expression was found incremented in group A, but SOD2 expression was decreased in groups A and B, comparative with controls. Group B presented significantly diminished levels of miR-421 and miR-200a, but only a decreasing trend on miR-34 and miR-206 expression was observed. Taken together, our findings demonstrated that besides DM, additional CVDRF presented a cumulative effect in the cellular response to oxidative unbalance, contributing to AMPK/SIRT1-PGC-1 alpha-SIRT3 pathway activation. SOD2, a major mitochondrial antioxidant defence, did not follow the same variation

Synergistically enhanced stability of laccase immobilized on synthesized silver nanoparticles with water-soluble polymers

"In Press, Accepted Manuscript, Available online 12 March 2017"Silver nanoparticles (AgNPs) were synthesized by citrate reduction method in the presence of polymers, poly(ethylene glycol) (PEG), poly(vinyl alcohol) (PVA) and chitosan, used as stabilizing agents, and an oxidoreductase enzyme, laccase (Lac), with the goal of expanding the NPs antimicrobial action. AgNPs were characterized by UV-visible spectrometry, dynamic light scattering and transmission electron microscopy. As protecting agents, PEG and PVA promoted the formation of spherical uniformly-shaped, small-sized, monodispersed AgNPs (≈ 20 nm). High Mw polymers were established as most effective in producing small-sized NPs. Chitosan's viscosity led to the formation of aggregates. Despite the decrease in Lac activity registered for the hybrid formulation, AgNPs-polymer-Lac, a significant augment in stability over time (up to 13 days, at 50 °C) was observed. This novel formulation displays improved synergistic performance over AgNPs-Lac or polymer-Lac conjugates, since in the former the Lac activity becomes residual at the end of 3 days. By enabling many ionic interactions, chitosan restricted the mass transfer between Lac and substrate and, thus, inhibited the enzymatic activity. These hybrid nanocomposites made up of inorganic NPs, organic polymers and immobilized antimicrobial oxidoreductive enzymes represent a new class of materials with improved synergistic performance. Moreover, the Lac and the AgNPs different antimicrobial action, both in time and mechanism, may also constitute a new alternative to reduce the probability of developing resistance-associated mutations.This work was funded by Portuguese Foundation for Science and TechnologyFCT/MCTES (PIDDAC) and co-financed by European funds (FEDER) through the PT2020 program, research projectM-ERA-NET/0006/2014. A. Zille and H. P. Felgueiras also acknowledge funding from FCT within the scope of the project POCI-01-0145-FEDER-007136 and UID/CTM/00264

Noether's Symmetry Theorem for Variational and Optimal Control Problems with Time Delay

We extend the DuBois-Reymond necessary optimality condition and Noether's symmetry theorem to the time delay variational setting. Both Lagrangian and Hamiltonian versions of Noether's theorem are proved, covering problems of the calculus of variations and optimal control with delays.Comment: This is a preprint of a paper whose final and definite form will appear in the international journal Numerical Algebra, Control and Optimization (NACO). Paper accepted for publication 15-March-201