Consequences of the Factorization Hypothesis in pbar p, pp, gamma p and gamma gamma Collisions

Using an eikonal analysis, we examine the validity of the factorization theorem for nucleon-nucleon, gamma p and gamma gamma collisions. As an example, using the additive quark model and meson vector dominance, we directly show that for all energies and values of the eikonal, that the factorization theorem sigma_{nn}/sigma_{gamma p} = sigma_{gamma p}/sigma_{gamma gamma} holds. We can also compute the survival probability of large rapidity gaps in high energy pbar p and pp collisions. We show that the survival probabilities are identical (at the same energy) for gamma p and gamma gamma collisions, as well as for nucleon-nucleon collisions. We further show that neither the factorization theorem nor the reaction-independence of the survival probabilities depends on the assumption of an additive quark model, but, more generally, depends on the opacity of the eikonal being independent of whether the reaction is n-n, gamma p or gamma gamma.Comment: 8 pages, Revtex, no figures. Expanded discussion, minor correction

Adaptation kinetics in bacterial chemotaxis

Cells of Escherichia coli, tethered to glass by a single flagellum, were subjected to constant flow of a medium containing the attractant alpha-methyl-DL-aspartate. The concentration of this chemical was varied with a programmable mixing apparatus over a range spanning the dissociation constant of the chemoreceptor at rates comparable to those experienced by cells swimming in spatial gradients. When an exponentially increasing ramp was turned on (a ramp that increases the chemoreceptor occupancy linearly), the rotational bias of the cells (the fraction of time spent spinning counterclockwise) changed rapidly to a higher stable level, which persisted for the duration of the ramp. The change in bias increased with ramp rate, i.e., with the time rate of change of chemoreceptor occupancy. This behavior can be accounted for by a model for adaptation involving proportional control, in which the flagellar motors respond to an error signal proportional to the difference between the current occupancy and the occupancy averaged over the recent past. Distributions of clockwise and counterclockwise rotation intervals were found to be exponential. This result cannot be explained by a response regular model in which transitions between rotational states are generated by threshold crossings of a regular subject to statistical fluctuation; this mechanism generates distributions with far too many long events. However, the data can be fit by a model in which transitions between rotational states are governed by first-order rate constants. The error signal acts as a bias regulator, controlling the values of these constants

Coordination of flagella on filamentous cells of Escherichia coli

Video techniques were used to study the coordination of different flagella on single filamentous cells of Escherichia coli. Filamentous, nonseptate cells were produced by introducing a cell division mutation into a strain that was polyhook but otherwise wild type for chemotaxis. Markers for its flagellar motors (ordinary polyhook cells that had been fixed with glutaraldehyde) were attached with antihook antibodies. The markers were driven alternately clockwise and counterclockwise, at angular velocities comparable to those observed when wild-type cells are tethered to glass. The directions of rotation of different markers on the same cell were not correlated; reversals of the flagellar motors occurred asynchronously. The bias of the motors (the fraction of time spent spinning counterclockwise) changed with time. Variations in bias were correlated, provided that the motors were within a few micrometers of one another. Thus, although the directions of rotation of flagellar motors are not controlled by a common intracellular signal, their biases are. This signal appears to have a limited range

Survival Probability of Large Rapidity Gaps in pbar p, pp, gamma p and gamma gamma Collisions

Using an eikonal analysis, we simultaneously fit a QCD-inspired parameterization of all accelerator data on forward proton-proton and antiproton-proton scattering amplitudes, together with cosmic ray data (using Glauber theory), to predict proton-air and proton-proton cross sections at energies near \sqrt s \approx 30 TeV. The p-air cosmic ray measurements greatly reduce the errors in the high energy proton-proton and proton-air cross section predictions--in turn, greatly reducing the errors in the fit parameters. From this analysis, we can then compute the survival probability of rapidity gaps in high energy pbar p and pp collisions, with high accuracy in a quasi model-free environment. Using an additive quark model and vector meson dominance, we note that that the survival probabilities are identical, at the same energy, for gamma p and gamma gamma collisions, as well as for nucleon-nucleon collisions. Significantly, our analysis finds large values for gap survival probabilities, \approx 30% at \sqrt s = 200 GeV, \approx 21% at \sqrt s = 1.8 TeV and \approx %%13% at \sqrt s = 14 TeV.Comment: 9 pages, Latex2e, uses epsfig.sty, 4 postscript figure

Controlling surface morphologies by time-delayed feedback

We propose a new method to control the roughness of a growing surface, via a time-delayed feedback scheme. As an illustration, we apply this method to the Kardar-Parisi-Zhang equation in 1+1 dimensions and show that the effective growth exponent of the surface width can be stabilized at any desired value in the interval [0.25,0.33], for a significant length of time. The method is quite general and can be applied to a wide range of growth phenomena. A possible experimental realization is suggested.Comment: 4 pages, 3 figure

EVALUATING THE EFFECTIVENESS OF INSTRUCTION IN ORAL HYGIENE FOR MENTALLY RETARDED BOYS

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/66133/1/j.1752-7325.1974.tb00668.x.pd

New limits on "odderon" amplitudes from analyticity constraints

In studies of high energy $pp$ and $\bar pp$ scattering, the odd (under crossing) forward scattering amplitude accounts for the difference between the $pp$ and $\bar pp$ cross sections. Typically, it is taken as $f_-=-\frac{p}{4\pi}Ds^{\alpha-1}e^{i\pi(1-\alpha)/2}$ ($\alpha\sim 0.5$), which has $\Delta\sigma, \Delta\rho\to0$ as $s\to\infty$, where $\rho$ is the ratio of the real to the imaginary portion of the forward scattering amplitude. However, the odd-signatured amplitude can have in principle a strikingly different behavior, ranging from having $\Delta\sigma\to$non-zero constant to having $\Delta\sigma \to \ln s/s_0$ as $s\to\infty$, the maximal behavior allowed by analyticity and the Froissart bound. We reanalyze high energy $pp$ and $\bar pp$ scattering data, using new analyticity constraints, in order to put new and precise limits on the magnitude of ``odderon'' amplitudes.Comment: 13 pages LaTex, 6 figure

New physics, the cosmic ray spectrum knee, and pppp cross section measurements

We explore the possibility that a new physics interaction can provide an explanation for the knee just above $10^6$ GeV in the cosmic ray spectrum. We model the new physics modifications to the total proton-proton cross section with an incoherent term that allows for missing energy above the scale of new physics. We add the constraint that the new physics must also be consistent with published $pp$ cross section measurements, using cosmic ray observations, an order of magnitude and more above the knee. We find that the rise in cross section required at energies above the knee is radical. The increase in cross section suggests that it may be more appropriate to treat the scattering process in the black disc limit at such high energies. In this case there may be no clean separation between the standard model and new physics contributions to the total cross section. We model the missing energy in this limit and find a good fit to the Tibet III cosmic ray flux data. We comment on testing the new physics proposal for the cosmic ray knee at the Large Hadron Collider.Comment: 17 pages, 4 figure

Psi-floor diagrams and a Caporaso-Harris type recursion

Floor diagrams are combinatorial objects which organize the count of tropical plane curves satisfying point conditions. In this paper we introduce Psi-floor diagrams which count tropical curves satisfying not only point conditions but also conditions given by Psi-classes (together with points). We then generalize our definition to relative Psi-floor diagrams and prove a Caporaso-Harris type formula for the corresponding numbers. This formula is shown to coincide with the classical Caporaso-Harris formula for relative plane descendant Gromov-Witten invariants. As a consequence, we can conclude that in our case relative descendant Gromov-Witten invariants equal their tropical counterparts.Comment: minor changes to match the published versio