Recognizing graphs close to bipartite graphs.

We continue research into a well-studied family of problems that ask if the vertices of a graph can be partitioned into sets A and B, where A is an independent set and B induces a graph from some specified graph class G. We let G be the class of k-degenerate graphs. The problem is known to be polynomial-time solvable if k=0 (bipartite graphs) and NP-complete if k=1 (near-bipartite graphs) even for graphs of diameter 4, as shown by Yang and Yuan, who also proved polynomial-time solvability for graphs of diameter 2. We show that recognizing near-bipartite graphs of diameter 3 is NP-complete resolving their open problem. To answer another open problem, we consider graphs of maximum degree D on n vertices. We show how to find A and B in O(n) time for k=1 and D=3, and in O(n^2) time for k >= 2 and D >= 4. These results also provide an algorithmic version of a result of Catlin [JCTB, 1979] and enable us to complete the complexity classification of another problem: finding a path in the vertex colouring reconfiguration graph between two given k-colourings of a graph of bounded maximum degree

Clique-width for graph classes closed under complementation.

Clique-width is an important graph parameter due to its algorithmic and structural properties. A graph class is hereditary if it can be characterized by a (not necessarily finite) set H of forbidden induced subgraphs. We initiate a systematic study into the boundedness of clique-width of hereditary graph classes closed under complementation. First, we extend the known classification for the |H|=1 case by classifying the boundedness of clique-width for every set H of self-complementary graphs. We then completely settle the |H|=2 case. In particular, we determine one new class of (H1, complement of H1)-free graphs of bounded clique-width (as a side effect, this leaves only six classes of (H1, H2)-free graphs, for which it is not known whether their clique-width is bounded). Once we have obtained the classification of the |H|=2 case, we research the effect of forbidding self-complementary graphs on the boundedness of clique-width. Surprisingly, we show that for a set F of self-complementary graphs on at least five vertices, the classification of the boundedness of clique-width for ({H1, complement of H1} + F)-free graphs coincides with the one for the |H|=2 case if and only if F does not include the bull (the only non-empty self-complementary graphs on fewer than five vertices are P_1 and P_4, and P_4-free graphs have clique-width at most 2). Finally, we discuss the consequences of our results for COLOURING

Row-switched states in two-dimensional underdamped Josephson junction arrays

When magnetic flux moves across layered or granular superconductor structures, the passage of vortices can take place along channels which develop finite voltage, while the rest of the material remains in the zero-voltage state. We present analytical studies of an example of such mixed dynamics: the row-switched (RS) states in underdamped two-dimensional Josephson arrays, driven by a uniform DC current under external magnetic field but neglecting self-fields. The governing equations are cast into a compact differential-algebraic system which describes the dynamics of an assembly of Josephson oscillators coupled through the mesh current. We carry out a formal perturbation expansion, and obtain the DC and AC spatial distributions of the junction phases and induced circulating currents. We also estimate the interval of the driving current in which a given RS state is stable. All these analytical predictions compare well with our numerics. We then combine these results to deduce the parameter region (in the damping coefficient versus magnetic field plane) where RS states can exist.Comment: latex, 48 pages, 15 figs using psfi

Arbuscular mycorrhizas are present on Spitsbergen

A previous study of 76 plant species on Spitsbergen in the High Arctic concluded that structures resembling arbuscular mycorrhizas were absent from roots. Here, we report a survey examining the roots of 13 grass and forb species collected from 12 sites on the island for arbuscular mycorrhizal (AM) colonisation. Of the 102 individuals collected, we recorded AM endophytes in the roots of 41 plants of 11 species (Alopecurus ovatus, Deschampsia alpina, Festuca rubra ssp. richardsonii, putative viviparous hybrids of Poa arctica and Poa pratensis, Poa arctica ssp. arctica, Trisetum spicatum, Coptidium spitsbergense, Ranunculus nivalis, Ranunculuspygmaeus, Ranunculus sulphureus and Taraxacum arcticum) sampled from 10 sites. Both coarse AM endophyte, with hyphae of 5–10 μm width, vesicles and occasional arbuscules, and fine endophyte, consisting of hyphae of 1–3 μm width and sparse arbuscules, were recorded in roots. Coarse AM hyphae, vesicles, arbuscules and fine endophyte hyphae occupied 1.0–30.7, 0.8–18.3, 0.7–11.9 and 0.7–12.8% of the root lengths of colonised plants, respectively. Principal component analysis indicated no associations between the abundances of AM structures in roots and edaphic factors. We conclude that the AM symbiosis is present in grass and forb roots on Spitsbergen

D* Production in Deep Inelastic Scattering at HERA

This paper presents measurements of D^{*\pm} production in deep inelastic scattering from collisions between 27.5 GeV positrons and 820 GeV protons. The data have been taken with the ZEUS detector at HERA. The decay channel $D^{*+}\to (D^0 \to K^- \pi^+) \pi^+$ (+ c.c.) has been used in the study. The $e^+p$ cross section for inclusive D^{*\pm} production with $5<Q^2<100 GeV^2$ and $y<0.7$ is 5.3 \pms 1.0 \pms 0.8 nb in the kinematic region {$1.3<p_T(D^{*\pm})<9.0$ GeV and $| \eta(D^{*\pm}) |<1.5$}. Differential cross sections as functions of p_T(D^{*\pm}), $\eta(D^{*\pm}), W$ and $Q^2$ are compared with next-to-leading order QCD calculations based on the photon-gluon fusion production mechanism. After an extrapolation of the cross section to the full kinematic region in p_T(D^{*\pm}) and $\eta$(D^{*\pm}), the charm contribution $F_2^{c\bar{c}}(x,Q^2)$ to the proton structure function is determined for Bjorken $x$ between 2 $\cdot$ 10$^{-4}$ and 5 $\cdot$ 10$^{-3}$.Comment: 17 pages including 4 figure

Observation of Scaling Violations in Scaled Momentum Distributions at HERA

Charged particle production has been measured in deep inelastic scattering (DIS) events over a large range of $x$ and $Q^2$ using the ZEUS detector. The evolution of the scaled momentum, $x_p$, with $Q^2,$ in the range 10 to 1280 $GeV^2$, has been investigated in the current fragmentation region of the Breit frame. The results show clear evidence, in a single experiment, for scaling violations in scaled momenta as a function of $Q^2$.Comment: 21 pages including 4 figures, to be published in Physics Letters B. Two references adde

Butterfly communities in miombo woodland: biodiversity declines with increaing woodland utilisation

Deforestation and degradation is threatening forests and woodlands globally. The deciduous miombo woodlands of sub-Saharan Africa are no exception, yet little is known about the flora and fauna they contain and the implications of their loss. Butterflies are recognised as indicators of environmental change; however the responses of butterflies in miombo woodlands have received little attention. This paper describes butterfly assemblages and their response to woodland utilisation in an understudied area of miombo woodland in south-west Tanzania. This is an area representative of miombo woodlands throughout sub-Saharan Africa, where woodland is utilised by local communities for a range of products, and is being rapidly converted to agriculture. Baited canopy traps and sweep nets were used to sample frugivorous and nectarivorous butterfly communities at different vertical stratifications in nine different study sites. 104 species were recorded, of which 16 are miombo specialists that have been recorded in Tanzania to the west of the country only. Indicator species were identified for three different levels of utilisation, with species from the sub-family Satyrinae indicating moderate utilisation. Generalised linear mixed effects models showed that butterfly species richness, diversity and abundance all decreased in response to increasing agriculture and anthropogenic utilisation. The loss of miombo woodlands is likely to result in declines in butterfly diversity. However, there was evidence of an intermediate disturbance effect for butterfly species richness, diversity and abundance with one utilisation variable, suggesting that a miombo woodland management plan that allows moderate sustainable utilisation in a heterogeneous landscape of mature miombo woodland and agriculture will simultaneously maintain butterfly communities and enable agricultural production