Shock waves in two-dimensional granular flow: effects of rough walls and polydispersity

We have studied the two-dimensional flow of balls in a small angle funnel, when either the side walls are rough or the balls are polydisperse. As in earlier work on monodisperse flows in smooth funnels, we observe the formation of kinematic shock waves/density waves. We find that for rough walls the flows are more disordered than for smooth walls and that shock waves generally propagate more slowly. For rough wall funnel flow, we show that the shock velocity and frequency obey simple scaling laws. These scaling laws are consistent with those found for smooth wall flow, but here they are cleaner since there are fewer packing-site effects and we study a wider range of parameters. For pipe flow (parallel side walls), rough walls support many shock waves, while smooth walls exhibit fewer or no shock waves. For funnel flows of balls with varying sizes, we find that flows with weak polydispersity behave qualitatively similar to monodisperse flows. For strong polydispersity, scaling breaks down and the shock waves consist of extended areas where the funnel is blocked completely.Comment: 11 pages, 15 figures; accepted for PR

Pseudomonas cannabina pv. cannabina pv. nov., and Pseudomonas cannabina pv. alisalensis (Cintas Koike and Bull, 2000) comb. nov., are members of the emended species Pseudomonas cannabina (ex Šutič & Dowson 1959) Gardan, Shafik, Belouin, Brosch, Grimont

Sequence similarity in the 16S rDNA gene confirmed that crucifer pathogen Pseudomonas syringae pv. alisalensis belongs to P. syringae sensu lato. In reciprocal DNA/DNA hybridization experiments, DNA relatedness was high (69–100%) between P. syringae pv. alisalensis strains and the type strain of P. cannabina (genomospecies 9). In contrast, DNA relatedness was low (below 48%) between P. syringae pv. alisalensis and reference strains from the remaining genomospecies of P. syringae including the type strain of P. syringae and reference strain of genomospecies 3 (P. syringae pv. tomato) although the well-known crucifer pathogen, P. syringae pv. maculicola, also belongs to genomospecies 3. Additional evidence that P. syringae pv. alisalensis belongs to P. cannabina was sequence similarity in five gene fragments used in multilocus sequence typing, as well as similar rep-PCR patterns when using the BOX-A1R primers. The description of P. cannabina has been emended to include P. syringae pv. alisalensis. Host range testing demonstrated that P. syringae pv. alisalensis strains, originally isolated from broccoli, broccoli raab or arugula, were not pathogenic on Cannabis sativa (family Cannabinaceae). Additionally, P. cannabina strains, originally isolated from the C. sativa were not pathogenic on broccoli raab or oat while P. syringae pv. alisalensis strains were pathogenic on these hosts. Distinct host ranges for these two groups indicate that P. cannabina emend. consists of at least two distinct pathovars, P. cannabina pv. cannabina pv. nov., and P. cannabina pv. alisalensis comb. nov. Pseudomonas syringae pv. maculicola strain CFBP 1637 is a member of P. cannabina

Complexity of Coloring Graphs without Paths and Cycles

Let $P_t$ and $C_\ell$ denote a path on $t$ vertices and a cycle on $\ell$ vertices, respectively. In this paper we study the $k$-coloring problem for $(P_t,C_\ell)$-free graphs. Maffray and Morel, and Bruce, Hoang and Sawada, have proved that 3-colorability of $P_5$-free graphs has a finite forbidden induced subgraphs characterization, while Hoang, Moore, Recoskie, Sawada, and Vatshelle have shown that $k$-colorability of $P_5$-free graphs for $k \geq 4$ does not. These authors have also shown, aided by a computer search, that 4-colorability of $(P_5,C_5)$-free graphs does have a finite forbidden induced subgraph characterization. We prove that for any $k$, the $k$-colorability of $(P_6,C_4)$-free graphs has a finite forbidden induced subgraph characterization. We provide the full lists of forbidden induced subgraphs for $k=3$ and $k=4$. As an application, we obtain certifying polynomial time algorithms for 3-coloring and 4-coloring $(P_6,C_4)$-free graphs. (Polynomial time algorithms have been previously obtained by Golovach, Paulusma, and Song, but those algorithms are not certifying); To complement these results we show that in most other cases the $k$-coloring problem for $(P_t,C_\ell)$-free graphs is NP-complete. Specifically, for $\ell=5$ we show that $k$-coloring is NP-complete for $(P_t,C_5)$-free graphs when $k \ge 4$ and $t \ge 7$; for $\ell \ge 6$ we show that $k$-coloring is NP-complete for $(P_t,C_\ell)$-free graphs when $k \ge 5$, $t \ge 6$; and additionally, for $\ell=7$, we show that $k$-coloring is also NP-complete for $(P_t,C_7)$-free graphs if $k = 4$ and $t\ge 9$. This is the first systematic study of the complexity of the $k$-coloring problem for $(P_t,C_\ell)$-free graphs. We almost completely classify the complexity for the cases when $k \geq 4, \ell \geq 4$, and identify the last three open cases

List of New Names of Plant Pathogenic Bacteria (2008-2010)

In 2010 the International Society of Plant Pathology Committee on the Taxonomy of Plant Pathogenic Bacteria published the Comprehensive List of Names of Plant Pathogenic Bacteria, 1980-2007 to provide an authoritative register of names of plant pathogens. In this manuscript we update the list of names by cataloguing names published from 2008 to 2010. We provide those names that have been validly and effectively published in this time frame, the proposed names that we judged to be invalid and names published earlier that did not make the previous lists. We also discuss problems that arise in the naming of strains that fall into the status Candidatus and nomenclatural problems in the genus Xanthomonas

List of New Names of Plant Pathogenic Bacteria (2011-2012)

The International Society of Plant Pathology Committee on the Taxonomy of Plant Pathogenic Bacteria has responsibility to evaluate the names of newly proposed pathovars for adherence to the International Standards for Naming Pathovars of Phytopathogenic Bacteria. Currently, the Comprehensive List of Names and the List of New Names of Plant Pathogenic Bacteria provide the authoritative register of names of bacterial plant pathogens. In this manuscript we up-date the list of names by cataloguing and evaluating names of plant pathogenic bacteria published in 2011 and 2012. We provide those names that have been validly and effectively published in this time frame, the proposed names that we judged to be invalid, and names published earlier that did not make the previous lists

List coloring in the absence of a linear forest.

The k-Coloring problem is to decide whether a graph can be colored with at most k colors such that no two adjacent vertices receive the same color. The Listk-Coloring problem requires in addition that every vertex u must receive a color from some given set L(u)⊆{1,…,k}. Let Pn denote the path on n vertices, and G+H and rH the disjoint union of two graphs G and H and r copies of H, respectively. For any two fixed integers k and r, we show that Listk-Coloring can be solved in polynomial time for graphs with no induced rP1+P5, hereby extending the result of Hoàng, Kamiński, Lozin, Sawada and Shu for graphs with no induced P5. Our result is tight; we prove that for any graph H that is a supergraph of P1+P5 with at least 5 edges, already List 5-Coloring is NP-complete for graphs with no induced H

First mineralogical maps of 4 Vesta

Before Dawn arrived at 4 Vesta only very low spatial resolution (~50 km) albedo and color maps were available from HST data. Also ground-based color and spectroscopic data were utilized as a first attempt to map Vesta’s mineralogical diversity [1-4]. The VIR spectrometer [5] onboard Dawn has ac-quired hyperspectral data while the FC camera [6] ob-tained multi-color data of the Vestan surface at very high spatial resolutions, allowing us to map complex geologic, morphologic units and features. We here re-port about the results obtained from a preliminary global mineralogical map of Vesta, based on data from the Survey orbit. This map is part of an iterative map-ping effort; the map is refined with each improvement in resolution

Out-of-equilibrium electromagnetic radiation

We derive general formulas for photon and dilepton production rates from an arbitrary non-equilibrated medium from first principles in quantum field theory. At lowest order in the electromagnetic coupling constant, these relate the rates to the unequal-time in-medium photon polarization tensor and generalize the corresponding expressions for a system in thermodynamic equilibrium. We formulate the question of electromagnetic radiation in real time as an initial value problem and consistently describe the virtual electromagnetic dressing of the initial state. In the limit of slowly evolving systems, we recover known expressions for the emission rates and work out the first correction to the static formulas in a systematic gradient expansion. Finally, we discuss the possible application of recently developed techniques in non-equilibrium quantum field theory to the problem of electromagnetic radiation. We argue, in particular, that the two-particle-irreducible (2PI) effective action formalism provides a powerful resummation scheme for the description of multiple scattering effects, such as the Landau-Pomeranchuk-Migdal suppression recently discussed in the context of equilibrium QCD.Comment: 34 pages, 9 figures, uses JHEP3.cl

Mapping the mineralogical composition of the Pinaria region (Av-11) of Vesta

We present the mineralogical map of a quadrant of the southern hemisphere of Vesta spanning 0-90 degrees longitude, and -21 to -66 degrees latitude; a region named Pinaria. The region, named after the Roman vestal virgin (c. 600 B.C.), includes an approximately 37km diameter crater, also named Pinaria. Several additional large craters are in this region as is the western most region of the rim of Rhea Silvia, named Matronalia Rupes. Mineralogical maps are based on data acquired by the Visible and Infrared Mapping Spectrometer (VIR-MS) and the Framing Camera (FC) on the Dawn spacecraft that has been orbiting Vesta since July 2011. VIR-MS is sensitive to wavelengths from 0.25um to 5.1um with a spatial resolution that depends upon the mission phase: nominally from 2.5 up to 0.8 km/pixel during the approach, 0.8 km/pixel during survey, 0.2 km/pixel during the high altitude orbit (HAMO) and about 0.05 km/pixel during the low altitude orbit (LAMO). This spatial resolution does not include the effects of the spacecraft's nor Vesta's motion. FC data from Survey orbit with a spatial resolution of about 250 m/pixel have been mapped using filter band parameters selected to enhance the anticipated mineralogy of Vesta. Global color maps of Vesta's surface using these color differences and ratios are generated. VIR data show that Vesta's surface is dominated by pyroxenes, with no evidence for the presence of other minerals observed at the scale of the survey measurements. The spectral parameters of the two major pyroxene absorption bands including band centers, depths and band areas and their variation within the Pinaria region, suggest mineralogical variation representing different compositional and/or textural terrains. Matronalia Rupes has band parameters suggesting different composition or grain size possibly resulting from down slope motion of regolith revealing different material beneath. The authors gratefully acknowledge the support of the Dawn Instrument, Operations, and Science Teams. This work is supported by an Italian Space Agency (ASI) grant, the DLR, MPI and by NASA through the Dawn project and the Dawn at Vesta Participating Scientist grant