Exclusive photoproduction of ϕ\phi meson in γp→ϕp\gamma p \to \phi p and pp→pϕpp p \to p \phi p reactions

The amplitude for $\gamma p \to \phi p$ is calculated in a pQCD $k_{T}$ - factorization approach. The total cross section for this process is compared with HERA data. Total cross section, as a function of photon-proton energy and photon virtuality, is calculated. We also discuss the ratio of $\sigma_{L}$ / $\sigma_{T}$ and the dependence on the mass of the strange quark. The amplitude for $\gamma p \to \phi p$ is used to predict the cross section for exclusive photoproduction of $\phi$ meson in proton-proton collisions. Absorption effects are included. The results for RHIC, Tevatron and LHC energies are presented.Comment: 10 pages, 5 figure

Production of Z^0 bosons with rapidity gaps: exclusive photoproduction in gamma p and p p collisions and inclusive double diffractive Z^0's

We extend the k_\perp-factorization formalism for exclusive photoproduction of vector mesons to the production of electroweak Z^0 bosons. Predictions for the gamma p \to Z^0 p and p p \to p p Z^0 reactions are given using an unintegrated gluon distribution tested against deep inelastic data. We present distributions in the Z^0 rapidity, transverse momentum of Z^0 as well as in relative azimuthal angle between outgoing protons. The contributions of different flavours are discussed. Absorption effects lower the cross section by a factor of 1.5-2, depending on the Z-boson rapidity. We also discuss the production of Z^0 bosons in central inclusive production. Here rapidity and (x_{\Pom,1}, x_{\Pom,2}) distributions of Z^0 are calculated. The corresponding cross section is about three orders of magnitude larger than that for the purely exclusive process.Comment: 19 pages, 14 figs, A. Cisek is married name of A. Rybarsk

The truth-telling motor cortex: Response competition in M1 discloses deceptive behaviour

Neural circuits associated with response conflict are active during deception. Here we use transcranial magnetic stimulation to examine for the first time whether competing responses in primary motor cortex can be used to detect lies. Participants used their little finger or thumb to respond either truthfully or deceitfully regarding facial familiarity. Motor-evoked-potentials (MEPs) from muscles associated with both digits tracked the development of each motor plan. When preparing to deceive, the MEP of the non-responding digit (i.e. the plan corresponding to the truth) exceeds the MEP of the responding digit (i.e. the lie), whereas a mirror-reversed pattern occurs when telling the truth. This give away response conflict interacts with the time of stimulation during a speeded reaction period. Lies can even activate digit-specific cortical representations when only verbal responses are made. Our findings support neurobiological models which blend cognitive decision-making with motor programming, and suggest a novel index for discriminating between honest and intentionally false facial recognition

Exclusive diffractive photoproduction of dileptons by timelike Compton scattering

We derive the forward photoproduction amplitude for the diffractive $\gamma p \to l^+ l^- p$ reaction in the momentum space. within the formalism of $k_\perp$- factorization. Predictions for the $\gamma p \to l^+ l^- p$ reaction are given using unintegrated gluon distribution from the literature. We calculate the total cross section as a function of photon-proton center of mass energy and the invariant mass distribution of the lepton pair. We also discuss whether the production of timelike virtual photons can be approximated by continuing to the spacelike domain $q^2 < 0$. The present calculation provides an input for future predictions for exclusive hadroproduction in the $p p \to p l^+ l^- p$ reaction.Comment: 11 pages, 7 figure

Exclusive coherent production of heavy vector mesons in nucleus-nucleus collisions at LHC

Heavy nuclei at collider energies are a source of high energy Weizsaecker-Williams photons. This photon flux may be utilized to study high energy photon-nucleus interactions. Here we concentrate on the coherent diffractive production of heavy vector mesons on nuclear targets and show how it probes the unintegrated glue of the nucleus in the saturation domain. We present predictions for rapidity distributions of exclusive coherent J/Psi and Upsilon mesons which can be measured by the ALICE experiment at the LHC.Comment: 17 pages, 12 eps figure

Free choice activates a decision circuit between frontal and parietal cortex

We often face alternatives that we are free to choose between. Planning movements to select an alternative involves several areas in frontal and parietal cortex that are anatomically connected into long-range circuits. These areas must coordinate their activity to select a common movement goal, but how neural circuits make decisions remains poorly understood. Here we simultaneously record from the dorsal premotor area (PMd) in frontal cortex and the parietal reach region (PRR) in parietal cortex to investigate neural circuit mechanisms for decision making. We find that correlations in spike and local field potential (LFP) activity between these areas are greater when monkeys are freely making choices than when they are following instructions. We propose that a decision circuit featuring a sub-population of cells in frontal and parietal cortex may exchange information to coordinate activity between these areas. Cells participating in this decision circuit may influence movement choices by providing a common bias to the selection of movement goals

fMRI evidence of ‘mirror’ responses to geometric shapes

Mirror neurons may be a genetic adaptation for social interaction [1]. Alternatively, the associative hypothesis [2], [3] proposes that the development of mirror neurons is driven by sensorimotor learning, and that, given suitable experience, mirror neurons will respond to any stimulus. This hypothesis was tested using fMRI adaptation to index populations of cells with mirror properties. After sensorimotor training, where geometric shapes were paired with hand actions, BOLD response was measured while human participants experienced runs of events in which shape observation alternated with action execution or observation. Adaptation from shapes to action execution, and critically, observation, occurred in ventral premotor cortex (PMv) and inferior parietal lobule (IPL). Adaptation from shapes to execution indicates that neuronal populations responding to the shapes had motor properties, while adaptation to observation demonstrates that these populations had mirror properties. These results indicate that sensorimotor training induced populations of cells with mirror properties in PMv and IPL to respond to the observation of arbitrary shapes. They suggest that the mirror system has not been shaped by evolution to respond in a mirror fashion to biological actions; instead, its development is mediated by stimulus-general processes of learning within a system adapted for visuomotor control

A simple optogenetic MAPK inhibitor design reveals resonance between transcription-regulating circuitry and temporally-encoded inputs

Engineering light-sensitive protein regulators has been a tremendous multidisciplinary challenge. Optogenetic regulators of MAPKs, central nodes of cellular regulation, have not previously been described. Here we present OptoJNKi, a light-regulated JNK inhibitor based on the AsLOV2 light-sensor domain using the ubiquitous FMN chromophore. OptoJNKi genetransfer allows optogenetic applications, whereas protein delivery allows optopharmacology. Development of OptoJNKi suggests a design principle for other optically regulated inhibitors. From this, we generate Optop38i, which inhibits p38MAPK in intact illuminated cells. Neurons are known for interpreting temporally-encoded inputs via interplay between ion channels, membrane potential and intracellular calcium. However, the consequences of temporal variation of JNK-regulating trophic inputs, potentially resulting from synaptic activity and reversible cellular protrusions, on downstream targets are unknown. Using OptoJNKi, we reveal maximal regulation of c-Jun transactivation can occur at unexpectedly slow periodicities of inhibition depending on the inhibitor's subcellular location. This provides evidence for resonance in metazoan JNK-signalling circuits

Intermittent control models of human standing: similarities and differences

Two architectures of intermittent control are compared and contrasted in the context of the single inverted pendulum model often used for describing standing in humans. The architectures are similar insofar as they use periods of open-loop control punctuated by switching events when crossing a switching surface to keep the system state trajectories close to trajectories leading to equilibrium. The architectures differ in two significant ways. Firstly, in one case, the open-loop control trajectory is generated by a system-matched hold, and in the other case, the open-loop control signal is zero. Secondly, prediction is used in one case but not the other. The former difference is examined in this paper. The zero control alternative leads to periodic oscillations associated with limit cycles; whereas the system-matched control alternative gives trajectories (including homoclinic orbits) which contain the equilibrium point and do not have oscillatory behaviour. Despite this difference in behaviour, it is further shown that behaviour can appear similar when either the system is perturbed by additive noise or the system-matched trajectory generation is perturbed. The purpose of the research is to come to a common approach for understanding the theoretical properties of the two alternatives with the twin aims of choosing which provides the best explanation of current experimental data (which may not, by itself, distinguish beween the two alternatives) and suggesting future experiments to distinguish between the two alternatives