A Note on Solid-State Maxwell Demon

Starting from 2002, at least two kinds of laboratory-testable, solid-state Maxwell demons have been proposed that utilize the electric field energy of an open-gap n-p junction and that seem to challenge the validity of the Second Law of Thermodynamics. In the present paper we present some arguments against the alleged functioning of such devices.Comment: 9 pages, 4 figures. Foundations of Physics, forthcoming. arXiv admin note: substantial text overlap with arXiv:1101.505

Production of neutral scalar Higgs bosons at eγe\gamma colliders

We study the production of neutral scalar (CP even) Higgs bosons in the process $e\gamma\to e h$ by including supersymmetric corrections to the dominant $t$-channel photon exchange amplitude. In addition to the standard model $W^{\pm}$ and fermion loops, there are substantial contributions from chargino loops. For some cases, these contributions can exceed those of the $W$'s and ordinary fermions. The cross sections in this channel are generally one or two orders of magnitude larger than those in the related channel $e\bar{e}\to\gamma h$.Comment: 12 pages RevTeX, 5 postscript figures included, uses epsf.st

Bounding the Hubble flow in terms of the w parameter

The last decade has seen increasing efforts to circumscribe and bound the cosmological Hubble flow in terms of model-independent constraints on the cosmological fluid - such as, for instance, the classical energy conditions of general relativity. Quite a bit can certainly be said in this regard, but much more refined bounds can be obtained by placing more precise constraints (either theoretical or observational) on the cosmological fluid. In particular, the use of the w-parameter (w=p/rho) has become increasingly common as a surrogate for trying to say something about the cosmological equation of state. Herein we explore the extent to which a constraint on the w-parameter leads to useful and nontrivial constraints on the Hubble flow, in terms of constraints on density rho(z), Hubble parameter H(z), density parameter Omega(z), cosmological distances d(z), and lookback time T(z). In contrast to other partial results in the literature, we carry out the computations for arbitrary values of the space curvature k in [-1,0,+1], equivalently for arbitrary Omega_0 <= 1.Comment: 15 page

Serologic evidence of occupational exposure to avian influenza viruses at the wildfowl/poultry/human interface

Ecological interactions between wild aquatic birds and outdoor-housed poultry can enhance spillover events of avian influenza viruses (AIVs) from wild reservoirs to domestic birds, thus increasing the related zoonotic risk to occupationally exposed workers. To assess serological evidence of AIV infection in workers operating in Northern Italy at the wildfowl/poultry interface or directly exposed to wildfowl, serum samples were collected between April 2005 and November 2006 from 57 bird-exposed workers (BEWs) and from 7 unexposed controls (Cs), planning three sample collec-tions from each individual. Concurrently, AIV surveillance of 3587 reared birds identified 4 AIVs belonging to H10N7, H4N6 and H2N2 subtypes while serological analysis by hemagglutination inhibition (HI) assay showed recent infections caused by H1, H2, H4, H6, H10, H11, H12, and H13 subtypes. Human sera were analyzed for specific antibodies against AIVs belonging to antigenic subtypes from H1 to H14 by using HI and virus microneutralization (MN) assays as a screening and a confirmatory test, respectively. Overall, antibodies specific to AIV-H3, AIV-H6, AIV-H8, and AIV-H9 were found in three poultry workers (PWs) and seropositivity to AIV-11, AIV-H13—still detectable in October 2017—in one wildlife professional (WP). Furthermore, seropositivity to AIV-H2, accounting for previous exposure to the “extinct” H2N2 human influenza viruses, was found in both BEWs and Cs groups. These data further emphasize the occupational risk posed by zoonotic AIV strains and show the possible occurrence of long-lived antibody-based immunity following AIV infections in humans

Muscle pain in mitochondrial diseases: a picture from the Italian network

Muscle pain may be part of many neuromuscular disorders including myopathies, peripheral neuropathies and lower motor neuron diseases. Although it has been reported also in mitochondrial diseases (MD), no extensive studies in this group of diseases have been performed so far. We reviewed clinical data from 1398 patients affected with mitochondrial diseases listed in the database of the "Nation-wide Italian Collaborative Network of Mitochondrial Diseases", to assess muscle pain and its features. Muscle pain was present in 164 patients (11.7%). It was commonly observed in subjects with chronic progressive external ophthalmoplegia (cPEO) and with primary myopathy without cPEO, but also-although less frequently-in multisystem phenotypes such as MELAS, MERFF, Kearns Sayre syndrome, NARP, MNGIE and Leigh syndrome. Patients mainly complain of diffuse exercise-related muscle pain, but focal/multifocal and at rest myalgia were often also reported. Muscle pain was more commonly detected in patients with mitochondrial DNA mutations (67.8%) than with nuclear DNA changes (32.2%). Only 34% of the patients showed a good response to drug therapy. Interestingly, patients with nuclear DNA mutations tend to have a better therapeutic response than patients with mtDNA mutations. Muscle pain is present in a significant number of patients with MD, being one of the most common symptoms. Although patients with a myopathic phenotype are more prone to develop muscle pain, this is also observed in patients with a multi system involvement, representing an important and disabling symptom having poor response to current therapy

Mass matrix Ansatz and lepton flavor violation in the THDM-III

Predictive Higgs-fermion couplings can be obtained when a specific texture for the fermion mass matrices is included in the general two-Higgs doublet model. We derive the form of these couplings in the charged lepton sector using a Hermitian mass matrix Ansatz with four-texture zeros. The presence of unconstrained phases in the vertices phi-li-lj modifies the pattern of flavor-violating Higgs interactions. Bounds on the model parameters are obtained from present limits on rare lepton flavor violating processes, which could be extended further by the search for the decay tau -> mu mu mu and mu-e conversion at future experiments. The signal from Higgs boson decays phi -> tau mu could be searched at the large hadron collider (LHC), while e-mu transitions could produce a detectable signal at a future e mu-collider, through the reaction e mu -> h0 -> tau tau.Comment: 17 pages, 9 figure

Detection of Neutral MSSM Higgs Bosons at LEP-II and NLC

We study the possibility of detecting the neutral Higgs bosons predicted in the Minimal Supersymmetric Standard Model (h0, H0, A0), with the reactions e+ e- --> b b h0 (H0, A0), using the helicity formalism. We analyze the region of parameter space (m_A0-tan beta) where h0(H0, A0) could be detected in the limit when tan beta is large. The numerical computation is done for the energy which is expected to be available at LEP-II (sqrt{s} = 200 GeV) and for a possible Next Linear e+ e- Collider (sqrt{s}=500 GeV).Comment: To be published in Phys.Rev.

Sensory Processing of Motor Inaccuracy Depends on Previously Performed Movement and on Subsequent Motor Corrections: A Study of the Saccadic System

When goal-directed movements are inaccurate, two responses are generated by the brain: a fast motor correction toward the target and an adaptive motor recalibration developing progressively across subsequent trials. For the saccadic system, there is a clear dissociation between the fast motor correction (corrective saccade production) and the adaptive motor recalibration (primary saccade modification). Error signals used to trigger corrective saccades and to induce adaptation are based on post-saccadic visual feedback. The goal of this study was to determine if similar or different error signals are involved in saccadic adaptation and in corrective saccade generation. Saccadic accuracy was experimentally altered by systematically displacing the visual target during motor execution. Post-saccadic error signals were studied by manipulating visual information in two ways. First, the duration of the displaced target after primary saccade termination was set at 15, 50, 100 or 800 ms in different adaptation sessions. Second, in some sessions, the displaced target was followed by a visual mask that interfered with visual processing. Because they rely on different mechanisms, the adaptation of reactive saccades and the adaptation of voluntary saccades were both evaluated. We found that saccadic adaptation and corrective saccade production were both affected by the manipulations of post-saccadic visual information, but in different ways. This first finding suggests that different types of error signal processing are involved in the induction of these two motor corrections. Interestingly, voluntary saccades required a longer duration of post-saccadic target presentation to reach the same amount of adaptation as reactive saccades. Finally, the visual mask interfered with the production of corrective saccades only during the voluntary saccades adaptation task. These last observations suggest that post-saccadic perception depends on the previously performed action and that the differences between saccade categories of motor correction and adaptation occur at an early level of visual processing