Selecting Base Points for the Schreier-Sims Algorithm for Matrix Groups

We consider the application of the Schreier-Sims algorithm and its variations to matrix groups defined over finite fields. We propose a new algorithm for the selection of the base points and demonstrate that it both improves the performance of the algorithm for a large range of examples and significantly extends the range of application. In particular, the random Schreier-Sims algorithm, with this enhancement, performs extremely well for almost simple groups.     

Learning from the West Coast: Long-Termism and Change – An Interview with Stewart Brand

Stewart Brand has been a key figure in the alternative culture of the US West Coast since the 1960s. The key message in his various publications has been that communities should be enabled to constantly reshape their own environments. In conversation with former Technical Editor of AD Peter Murray , he describes his lifestyle and influences – from the hippy movement, to time working for California Governor Jerry Brown in the 1970s, to writers such as Gregory Bateson, Frank Duffy and Christopher Alexander – and advocates a loose-fit ‘architecture of systems’, rather than a fixed and limiting ‘architecture of moulds’.     

Floating Ring Stabilization System

The necessity of magnetically levitating a superconducting, current carrying ring without mechanical supports requires an electrical stabilizing system. The ring, when supported, has only one equilibrium position and this position is one of unstable equilibrium. The ring is free to move with up to six degrees of freedom. Two degrees are dictated by the ability of the ring to move in any direction in the plane of the ring. Additionally, the ring can be tilted requiring three more reference points to determine a new plane. The sixth degree of freedom is the ability of the ring to rotate upon its own axis, but because external forces tending to cause this rotation can, in principal, be eliminated, a restoring supply is not provided. Each of the five identical stabilizing supplies in this system has a feedback loop composed of the following segments. The position detector element is an optical head which sends a light beam across an optical edge on the ring, the reflection of which is sensed on a photo diode. This diode voltage signal, proportional to the ring position, is the input to an amplifier whose output is a signal proportional to position, velocity and ring acceleration. A 50 volt, 100 ampere, bidirectional dc transistor power supply is activated from this signal which in turn powers the appropriate stabilizing coil located near the floating current carrying ring.     

Substituted glycals as probes of glycosidase mechanisms

D-Glucal and a series of substituted derivatives have been tested as substrates, inhibitors and inactivators of the Agrobacterium faecalis beta-glucosidase in order to probe structure/function relationships in this enzyme. D-Glucal is shown to be a substrate (kcat = 2.3 min-1, Km = 0.85 mM) undergoing hydration with stereospecific protonation from the alpha-face to yield 2-deoxy-beta-D-glucose. 1-Methyl-D-glucal surprisingly serves as only a poor substrate (kcat = 0.056 min-1, Km = 57 mM), also undergoing protonation from the alpha-face. 2-Fluoro-D-glucal, however is completely inert, as a result of inductive destabilisation of the oxocarbenium ion-like transition state for protonation, and functions only as a relatively weak (Ki = 24 mM) inhibitor. Similar behaviour was seen with almond beta-glucosidase and yeast alpha-glucosidase and for the interaction of 2-fluoro-D-galactal with Escherichia coli beta-galactosidase. A series of of alpha, beta-unsaturated glucal derivatives was also synthesised and tested as potential substrates, inhibitors or inactivators of A. faecalis beta-glucosidase. Of these only 1-nitro-D-glucal functioned as a time dependent, irreversible inactivator (ki = 0.011 min-1, Ki = 5.5 mM), presumably acting as a Michael acceptor. Electrospray mass spectrometric analysis revealed multiple labeling of the enzyme by this inactivator, lessening its usefulness as an affinity label. Less reactive Michael acceptor glycals which might have been more specific (1-cyano-, 2-cyano-, 1-carboxylic acid, 1-carboxylic acid methyl ester) unfortunately did not function as inactivators or substrates, only as relatively weak reversible inhibitors (Ki = 3-96 mM).     

Radionuclides in the Kara sea bottom sediments

The contents and distribution of natural (214Pb, 214Bi, 228Ac, and 208Tl) and technogenic (90Sr, 137Cs, and 60Co) radionuclides in the Kara Sea bottom sediments was analyzed by using the materials collected by R/V "Pomor" (Murmansk Marine Biological Institute). In 1994, no high (critical) concentrations of technogenic radioisotopes were found in the sea sediments, while the spots (regions) of elevated 137Cs content found in 1984 were not confirmed in 1994. It was proposed that the main sources of entry of technogenic radionuclides in the sea sediments in the last years are the flow of the Ob'-Yenisei waters and container burials of radioactive waste in the sea, which appeared to have been markedly corroded. The latter is confirmed by detection in some places of 60Co, which was not previously found in the sediments.     

符合贸易要求的车载称重

在过去的10年中,NORAC系统国际组织从设想中形成一套车载称重理念,许多人都认为要想达到商业的真实性是不可能的.     

Lipidomic Approaches to Study HDL Metabolism in Patients with Central Obesity Diagnosed with Metabolic Syndrome

The metabolic syndrome (MetS) is a cluster of cardiovascular risk factors characterised by central obesity, atherogenic dyslipidaemia, and changes in the circulating lipidome; the underlying mechanisms that lead to this lipid remodelling have only been partially elucidated. This study used an integrated “omics” approach (untargeted whole serum lipidomics, targeted proteomics, and lipoprotein lipidomics) to study lipoprotein remodelling and HDL composition in subjects with central obesity diagnosed with MetS (vs. controls). Compared with healthy subjects, MetS patients showed higher free fatty acids, diglycerides, phosphatidylcholines, and triglycerides, particularly those enriched in products of de novo lipogenesis. On the other hand, the “lysophosphatidylcholines to phosphatidylcholines” and “cholesteryl ester to free cholesterol” ratios were reduced, pointing to a lower activity of lecithin cholesterol acyltransferase (LCAT) in MetS; LCAT activity (directly measured and predicted by lipidomic ratios) was positively correlated with high-density lipoprotein cholesterol (HDL-C) and negatively correlated with body mass index (BMI) and insulin resistance. Moreover, many phosphatidylcholines and sphingomyelins were significantly lower in the HDL of MetS patients and strongly correlated with BMI and clinical metabolic parameters. These results suggest that MetS is associated with an impairment of phospholipid metabolism in HDL, partially led by LCAT, and associated with obesity and underlying insulin resistance. This study proposes a candidate strategy to use integrated “omics” approaches to gain mechanistic insights into lipoprotein remodelling, thus deepening the knowledge regarding the molecular basis of the association between MetS and atherosclerosis.     

Large-scale parallel arrays of silicon nanowires via block copolymer directed self-assembly

Extending the resolution and spatial proximity of lithographic patterning below critical dimensions of 20 nm remains a key challenge with very-large-scale integration, especially if the persistent scaling of silicon electronic devices is sustained. One approach, which relies upon the directed self-assembly of block copolymers by chemical-epitaxy, is capable of achieving high density 1?:?1 patterning with critical dimensions approaching 5 nm. Herein, we outline an integration-favourable strategy for fabricating high areal density arrays of aligned silicon nanowires by directed self-assembly of a PS-b-PMMA block copolymer nanopatterns with a L(0) (pitch) of 42 nm, on chemically pre-patterned surfaces. Parallel arrays (5 × 10(6) wires per cm) of uni-directional and isolated silicon nanowires on insulator substrates with critical dimension ranging from 15 to 19 nm were fabricated by using precision plasma etch processes; with each stage monitored by electron microscopy. This step-by-step approach provides detailed information on interfacial oxide formation at the device silicon layer, the polystyrene profile during plasma etching, final critical dimension uniformity and line edge roughness variation nanowire during processing. The resulting silicon-nanowire array devices exhibit Schottky-type behaviour and a clear field-effect. The measured values for resistivity and specific contact resistance were ((2.6 ± 1.2) × 10(5)Ωcm) and ((240 ± 80) Ωcm(2)) respectively. These values are typical for intrinsic (un-doped) silicon when contacted by high work function metal albeit counterintuitive as the resistivity of the starting wafer (～10 Ωcm) is 4 orders of magnitude lower. In essence, the nanowires are so small and consist of so few atoms, that statistically, at the original doping level each nanowire contains less than a single dopant atom and consequently exhibits the electrical behaviour of the un-doped host material. Moreover this indicates that the processing successfully avoided unintentional doping. Therefore our approach permits tuning of the device steps to contact the nanowires functionality through careful selection of the initial bulk starting material and/or by means of post processing steps e.g. thermal annealing of metal contacts to produce high performance devices. We envision that such a controllable process, combined with the precision patterning of the aligned block copolymer nanopatterns, could prolong the scaling of nanoelectronics and potentially enable the fabrication of dense, parallel arrays of multi-gate field effect transistors.     

Studies in Germanium Oxide Systems: I, Phase Equilibria in the System Li2O—GeO2

Phase equilibrium relations in the system Li₂O-GeO₂ were determined using standard quenching techniques. In contrast to published literature five congruently melting compounds were found to exist. They are Li₂O·7GeO₂, 3Li₂O O·8GeO₂, Li₂O O·GeO₂, 3Li₂O O·2GeO₂, and 2Li₂O.-GeO₂. The melting points, respectively, are 1033°± 5°C, 953°± 5°C, 1245°± 15°C, 1125°± 15°C, and 1280°± 15°C. Simple binary eutectic relations exist among the compounds. The eutectic temperature between 1:7 and GeO₂ is 1025°± 1h0°C at about 96.8 wt% GeO₂; the eutectic temperature between the 1:7 and 3:8 compounds is 935°± 10°C at about 90.9 wt% GeO₂; the eutectic temperature between the 3:8 and 1:1 compounds is 930°± 10 °C at about 89.8 wt% GeO₂. Liquidus data for compositions richer in lithia than the 1:1 compound are only approximate because of the difficulty of quenching them; the phase relations between the 1:1 and 3:2 and between the 3:2 and 2:l compounds, however, are found to be of the simple binary eutectic type. The glass–forming region was also determined. Melts allowed to cool in air crystallized. When, however, the melts were quenched, glasses containing as much as 8 wt% GeO₂ could be prepared in 5–g quantities. Both the refractive index–composition and density–composition curves for the glasses showed maxi–mums at about 6 to 8 wt% Li₂O.