Time-dependent spectral-feature variations of stars displaying the B[e] phenomenon; I. V2028 Cyg

We present results of nearly six years of spectroscopic observations of the B[e] star V2028 Cyg. The presence of the cold-type absorption lines combined with a hot-type spectrum indicate the binarity of this object. Since B[e] stars are embedded in an extended envelope, the usage of common stellar atmosphere models for the analysis is quite inappropriate. Therefore, we focus on the analysis of the long-term spectral line variations in order to determine the nature of this object. We present the time dependences of the equivalent width and radial velocities of the H alpha line, [O I] 6300 A, Fe II 6427, 6433, and 6456 A lines. The bisector variations and line intensities are shown for the H alpha line. The radial velocities are also measured for the absorption lines of the K component. No periodic variation is found. The observed data show correlations between the measured quantities, which can be used in future modelling

On Invariant Notions of Segre Varieties in Binary Projective Spaces

Invariant notions of a class of Segre varieties \Segrem(2) of PG(2^m - 1, 2) that are direct products of $m$ copies of PG(1, 2), $m$ being any positive integer, are established and studied. We first demonstrate that there exists a hyperbolic quadric that contains \Segrem(2) and is invariant under its projective stabiliser group \Stab{m}{2}. By embedding PG(2^m - 1, 2) into \PG(2^m - 1, 4), a basis of the latter space is constructed that is invariant under \Stab{m}{2} as well. Such a basis can be split into two subsets whose spans are either real or complex-conjugate subspaces according as $m$ is even or odd. In the latter case, these spans can, in addition, be viewed as indicator sets of a \Stab{m}{2}-invariant geometric spread of lines of PG(2^m - 1, 2). This spread is also related with a \Stab{m}{2}-invariant non-singular Hermitian variety. The case $m=3$ is examined in detail to illustrate the theory. Here, the lines of the invariant spread are found to fall into four distinct orbits under \Stab{3}{2}, while the points of PG(7, 2) form five orbits.Comment: 18 pages, 1 figure; v2 - version accepted in Designs, Codes and Cryptograph

Constraining Antimatter Domains in the Early Universe with Big Bang Nucleosynthesis

We consider the effect of a small-scale matter-antimatter domain structure on big bang nucleosynthesis and place upper limits on the amount of antimatter in the early universe. For small domains, which annihilate before nucleosynthesis, this limit comes from underproduction of He-4. For larger domains, the limit comes from He-3 overproduction. Most of the He-3 from antiproton-helium annihilation is annihilated also. The main source of He-3 is photodisintegration of He-4 by the electromagnetic cascades initiated by the annihilation.Comment: 4 pages, 2 figures, revtex, (slightly shortened

Investigation of Mitochondrial Dysfunction by Sequential Microplate-Based Respiration Measurements from Intact and Permeabilized Neurons

Mitochondrial dysfunction is a component of many neurodegenerative conditions. Measurement of oxygen consumption from intact neurons enables evaluation of mitochondrial bioenergetics under conditions that are more physiologically realistic compared to isolated mitochondria. However, mechanistic analysis of mitochondrial function in cells is complicated by changing energy demands and lack of substrate control. Here we describe a technique for sequentially measuring respiration from intact and saponin-permeabilized cortical neurons on single microplates. This technique allows control of substrates to individual electron transport chain complexes following permeabilization, as well as side-by-side comparisons to intact cells. To illustrate the utility of the technique, we demonstrate that inhibition of respiration by the drug KB-R7943 in intact neurons is relieved by delivery of the complex II substrate succinate, but not by complex I substrates, via acute saponin permeabilization. In contrast, methyl succinate, a putative cell permeable complex II substrate, failed to rescue respiration in intact neurons and was a poor complex II substrate in permeabilized cells. Sequential measurements of intact and permeabilized cell respiration should be particularly useful for evaluating indirect mitochondrial toxicity due to drugs or cellular signaling events which cannot be readily studied using isolated mitochondria

Potentiation of the glutamatergic synaptic input to rat locus coeruleus neurons by P2X7 receptors

Locus coeruleus (LC) neurons in a rat brain slice preparation were superfused with a Mg2+-free and bicuculline-containing external medium. Under these conditions, glutamatergic spontaneous excitatory postsynaptic currents (sEPSCs) were recorded by means of the whole-cell patch-clamp method. ATP, as well as its structural analogue 2-methylthio ATP (2-MeSATP), both caused transient inward currents, which were outlasted by an increase in the frequency but not the amplitude of the sEPSCs. PPADS, but not suramin or reactive blue 2 counteracted both effects of 2-MeSATP. By contrast, α,β-methylene ATP (α,β-meATP), UTP and BzATP did not cause an inward current response. Of these latter agonists, only BzATP slightly facilitated the sEPSC amplitude and strongly potentiated its frequency. PPADS and Brilliant Blue G, as well as fluorocitric acid and aminoadipic acid prevented the activity of BzATP. Furthermore, BzATP caused a similar facilitation of the miniature (m)EPSC (recorded in the presence of tetrodotoxin) and sEPSC frequencies (recorded in its absence). Eventually, capsaicin augmented the frequency of the sEPSCs in a capsazepine-, but not PPADS-antagonizable, manner. In conclusion, the stimulation of astrocytic P2X7 receptors appears to lead to the outflow of a signalling molecule, which presynaptically increases the spontaneous release of glutamate onto LC neurons from their afferent fibre tracts. It is suggested, that the two algogenic compounds ATP and capsaicin utilise separate receptor systems to potentiate the release of glutamate and in consequence to increase the excitability of LC neurons. © 2010 Springer Science+Business Media B.V

Black Hole Entropy and Finite Geometry

It is shown that the $E_{6(6)}$ symmetric entropy formula describing black holes and black strings in D=5 is intimately tied to the geometry of the generalized quadrangle GQ$(2,4)$ with automorphism group the Weyl group $W(E_6)$. The 27 charges correspond to the points and the 45 terms in the entropy formula to the lines of GQ$(2,4)$. Different truncations with $15, 11$ and 9 charges are represented by three distinguished subconfigurations of GQ$(2,4)$, well-known to finite geometers; these are the "doily" (i. e. GQ$(2,2)$) with 15, the "perp-set" of a point with 11, and the "grid" (i. e. GQ$(2,1)$) with 9 points, respectively. In order to obtain the correct signs for the terms in the entropy formula, we use a non- commutative labelling for the points of GQ$(2,4)$. For the 40 different possible truncations with 9 charges this labelling yields 120 Mermin squares -- objects well-known from studies concerning Bell-Kochen-Specker-like theorems. These results are connected to our previous ones obtained for the $E_{7(7)}$ symmetric entropy formula in D=4 by observing that the structure of GQ$(2,4)$ is linked to a particular kind of geometric hyperplane of the split Cayley hexagon of order two, featuring 27 points located on 9 pairwise disjoint lines (a distance-3-spread). We conjecture that the different possibilities of describing the D=5 entropy formula using Jordan algebras, qubits and/or qutrits correspond to employing different coordinates for an underlying non-commutative geometric structure based on GQ$(2,4)$.Comment: 17 pages, 3 figures, v2 a new paragraph added, typos correcte

Soil and water bioengineering: practice and research needs for reconciling natural hazard control and ecological restoration

Soil and water bioengineering is a technology that encourages scientists and practitioners to combine their knowledge and skills in the management of ecosystems with a common goal to maximize benefits to both man and the natural environment. It involves techniques that use plants as living building materials, for: (i) natural hazard control (e.g., soil erosion, torrential floods and landslides) and (ii) ecological restoration or nature-based re-introduction of species on degraded lands, river embankments, and disturbed environments. For a bioengineering project to be successful, engineers are required to highlight all the potential benefits and ecosystem services by documenting the technical, ecological, economic and social values. The novel approaches used by bioengineers raise questions for researchers and necessitate innovation from practitioners to design bioengineering concepts and techniques. Our objective in this paper, therefore, is to highlight the practice and research needs in soil and water bioengineering for reconciling natural hazard control and ecological restoration. Firstly, we review the definition and development of bioengineering technology, while stressing issues concerning the design, implementation, and monitoring of bioengineering actions. Secondly, we highlight the need to reconcile natural hazard control and ecological restoration by posing novel practice and research questions