The Meridional Thermospheric Neutral Wind Measured by Radar and Optical Techniques in the Auroral Region

Radar observations of ion velocities in the magnetic zenith over Chatanika, Alaska, were used to determine the geomagnetic meridional component of the thermospheric neutral wind. Corrections for molecular diffusion and molecular ion contamination of the pure O+ composition assumed for the ionosphere were included in the analysis. Comparison of the averaged diurnal variation of the meridional wind showed good agreement between the two measurement techniques. Good agreement was also found for several cases of simultaneous observations. The evidence suggested that differences were caused by gravity waves. The 7 years of radar meridional wind results were examined with respect to magnetic activity, solar cycle phase, and season. During the day, the meridional component is poleward with a maximum of about 65 m/s between 1400 and 1600 local time. During the night, the wind is equatorward with a maximum of about 175 m/s between 0200 and 0500 local time. This maximum occurs after local magnetic midnight, which is about 0130 local time. When the neutral wind is averaged for 24 hours, there is a large net equatorward flow. During periods of increased magnetic activity, the nighttime wind between 2300 and 0600 local time becomes stronger toward the equator. The average increase between 0200 and 0600 local time is about 100 m/s; however, on individual days it can be as large as 400 m/s. These data pertain mostly to equinox, but the few summer and winter observations in the data set differ in the manner predicted by theory. Comparison of these results with theoretical models shows good agreement at most times, but suggests possible heating poleward of Chatanika during the morning hours. Observed exospheric temperature increases support this hypothesis

Ordering variable for parton showers

The parton splittings in a parton shower are ordered according to an ordering variable, for example the transverse momentum of the daughter partons relative to the direction of the mother, the virtuality of the splitting, or the angle between the daughter partons. We analyze the choice of the ordering variable and conclude that one particular choice has the advantage of factoring softer splittings from harder splittings graph by graph in a physical gauge.Comment: 28 pages, 5 figure

Coherent States of the q--Canonical Commutation Relations

For the $q$-deformed canonical commutation relations $a(f)a^\dagger(g) = (1-q)\,\langle f,g\rangle{\bf1}+q\,a^\dagger(g)a(f)$ for $f,g$ in some Hilbert space ${\cal H}$ we consider representations generated from a vector $\Omega$ satisfying $a(f)\Omega=\langle f,\phi\rangle\Omega$, where $\phi\in{\cal H}$. We show that such a representation exists if and only if $\Vert\phi\Vert\leq1$. Moreover, for $\Vert\phi\Vert<1$ these representations are unitarily equivalent to the Fock representation (obtained for $\phi=0$). On the other hand representations obtained for different unit vectors $\phi$ are disjoint. We show that the universal C*-algebra for the relations has a largest proper, closed, two-sided ideal. The quotient by this ideal is a natural $q$-analogue of the Cuntz algebra (obtained for $q=0$). We discuss the Conjecture that, for $d<\infty$, this analogue should, in fact, be equal to the Cuntz algebra itself. In the limiting cases $q=\pm1$ we determine all irreducible representations of the relations, and characterize those which can be obtained via coherent states.Comment: 19 pages, Plain Te

Adaptive response and enlargement of dynamic range

Many membrane channels and receptors exhibit adaptive, or desensitized, response to a strong sustained input stimulus, often supported by protein activity-dependent inactivation. Adaptive response is thought to be related to various cellular functions such as homeostasis and enlargement of dynamic range by background compensation. Here we study the quantitative relation between adaptive response and background compensation within a modeling framework. We show that any particular type of adaptive response is neither sufficient nor necessary for adaptive enlargement of dynamic range. In particular a precise adaptive response, where system activity is maintained at a constant level at steady state, does not ensure a large dynamic range neither in input signal nor in system output. A general mechanism for input dynamic range enlargement can come about from the activity-dependent modulation of protein responsiveness by multiple biochemical modification, regardless of the type of adaptive response it induces. Therefore hierarchical biochemical processes such as methylation and phosphorylation are natural candidates to induce this property in signaling systems.Comment: Corrected typos, minor text revision

Phase Structure and Compactness

In order to study the influence of compactness on low-energy properties, we compare the phase structures of the compact and non-compact two-dimensional multi-frequency sine-Gordon models. It is shown that the high-energy scaling of the compact and non-compact models coincides, but their low-energy behaviors differ. The critical frequency $\beta^2 = 8\pi$ at which the sine-Gordon model undergoes a topological phase transition is found to be unaffected by the compactness of the field since it is determined by high-energy scaling laws. However, the compact two-frequency sine-Gordon model has first and second order phase transitions determined by the low-energy scaling: we show that these are absent in the non-compact model.Comment: 21 pages, 5 figures, minor changes, final version, accepted for publication in JHE

Double Parton Scattering Singularity in One-Loop Integrals

We present a detailed study of the double parton scattering (DPS) singularity, which is a specific type of Landau singularity that can occur in certain one-loop graphs in theories with massless particles. A simple formula for the DPS singular part of a four-point diagram with arbitrary internal/external particles is derived in terms of the transverse momentum integral of a product of light cone wavefunctions with tree-level matrix elements. This is used to reproduce and explain some results for DPS singularities in box integrals that have been obtained using traditional loop integration techniques. The formula can be straightforwardly generalised to calculate the DPS singularity in loops with an arbitrary number of external particles. We use the generalised version to explain why the specific MHV and NMHV six-photon amplitudes often studied by the NLO multileg community are not divergent at the DPS singular point, and point out that whilst all NMHV amplitudes are always finite, certain MHV amplitudes do contain a DPS divergence. It is shown that our framework for calculating DPS divergences in loop diagrams is entirely consistent with the `two-parton GPD' framework of Diehl and Schafer for calculating proton-proton DPS cross sections, but is inconsistent with the `double PDF' framework of Snigirev.Comment: 29 pages, 8 figures. Minor corrections and clarifications added. Version accepted for publication in JHE

Transcriptional Regulation Is a Major Controller of Cell Cycle Transition Dynamics

DNA replication, mitosis and mitotic exit are critical transitions of the cell cycle which normally occur only once per cycle. A universal control mechanism was proposed for the regulation of mitotic entry in which Cdk helps its own activation through two positive feedback loops. Recent discoveries in various organisms showed the importance of positive feedbacks in other transitions as well. Here we investigate if a universal control system with transcriptional regulation(s) and post-translational positive feedback(s) can be proposed for the regulation of all cell cycle transitions. Through computational modeling, we analyze the transition dynamics in all possible combinations of transcriptional and post-translational regulations. We find that some combinations lead to ‘sloppy’ transitions, while others give very precise control. The periodic transcriptional regulation through the activator or the inhibitor leads to radically different dynamics. Experimental evidence shows that in cell cycle transitions of organisms investigated for cell cycle dependent periodic transcription, only the inhibitor OR the activator is under cyclic control and never both of them. Based on these observations, we propose two transcriptional control modes of cell cycle regulation that either STOP or let the cycle GO in case of a transcriptional failure. We discuss the biological relevance of such differences

Next-to-leading order QCD predictions for W+W+jj production at the LHC

Because the LHC is a proton-proton collider, sizable production of two positively charged W-bosons in association with two jets is possible. This process leads to a distinct signature of same sign high-pt leptons, missing energy and jets. We compute the NLO QCD corrections to the QCD-mediated part of pp -> W+W+jj. These corrections reduce the dependence of the production cross-section on the renormalization and factorization scale to about +- 10 percent. We find that a large number of W+W+jj events contain a relatively hard third jet. The presence of this jet should help to either pick up the W+W+jj signal or to reject it as an unwanted background.Comment: 15 pages, 5 (lovely) figures, v3 accepted for publication in JHEP, corrects tables in appendi

Electron Density Distributions in Saturn's Ionosphere

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.Between 26 April and 15 September 2017, Cassini executed 23 highly inclined Grand Finale orbits through a new frontier for space exploration, the narrow region between Saturn and the D Ring, providing the first opportunity for obtaining in situ ionospheric measurements. During the Grand Finale orbits, the Radio and Plasma Wave Science instrument observed broadband whistler mode emissions and narrowband upper hybrid frequency emissions. Using known wave propagation characteristics of these two plasma wave modes, the electron density is derived over a broad range of ionospheric latitudes and altitudes. A two‐part exponential scale height model is fitted to the electron density measurements. The model yields a double‐layered ionosphere with plasma scale heights of 545/575 km for the northern/southern hemispheres below 4,500 km and plasma scale heights of 4,780/2,360 km for the northern/southern hemispheres above 4,500 km. The interpretation of these layers involves the interaction between the rings and the ionosphere