Aircraft computations using multigrid and an unstructured parallel library

This paper examines the application of unstructured multigrid, using a sequence of independent tetrahedral grids. The test cases examined are for inviscid flow over an aircraft and an M6 wing. The sensitivity of the method to grid sequence and cycling strategy are investigated. \ud \ud All of the calculations were performed on a parallel computer. This was achieved by using the OPlus library which, by the straightforward insertion of subroutine calls, facilitates parallelisation of the resulting code. A single source OPlus application code can be compiled to executed on either a parallel or sequential machine. This greatly increases the usability of the parallel machine, and the maintainability of the code

Anti-PrP antibodies block PrPSc replication in prion-infected cell cultures by accelerating PrPC degradation.

manuscript received October 15, 2003; revised manuscript received December 15, 2003; accepted December 16, 2003. We thanks P. Rondard, O Bischof, J.-L. Laplanche and J.-P. Pin for their fruitful discussions. we are grateful to S. barrère for her assistance in the statistical analysis of the data and H. McMahon for her assistance in reading the manuscript

Solubilization of pig lymphocyte plasma membrane and fractionation of some of the components

The degree of solubilization of pig lymphocyte plasma membrane by sodium deoxycholate was determined at a variety of temperatures and detergent concentrations. Approx. 95% of the membrane protein was soluble in 2% deoxycholate at 23°C. Some of the biological activities of the membrane survived this treatment. The leucine β-naphthylamidase activity was more readily soluble than the 5′-nucleotidase and these enzymes could be separated by extraction with 0.5% deoxycholate at 0°C. Membrane solubilized in 2% deoxycholate at 23°C was fractionated by sucrose-density-gradient centrifugation in 1% deoxycholate. The phospholipid was separated from the protein, which formed a fairly symmetrical peak that sedimented slightly slower than ovalbumin; the leucine naphthylamidase and 5′-nucleotidase activities were resolved from each other and from the main protein peak. Similar separations were achieved by elution from Sephadex G-200 and Sepharose 6B in 1% deoxycholate. The main proteins, however, appeared to possess much higher molecular weights than those indicated by sucrose-density-gradient centrifugation. This disparity suggests that many of the membrane proteins have a rod-like shape, especially since the results of experiments with [14C]deoxycholate revealed that the proteins did not bind significant amounts of deoxycholate. In contrast, 5′-nucleotidase and leucine naphthylamidase appeared to be globular. Polyacrylamide-gel electrophoresis of membrane solubilized in sodium dodecyl sulphate gave a similar distribution of protein to that achieved by sucrose-density-gradient centrifugation. Trace amounts only of polypeptides of molecular weight less than 10000 were detected.</jats:p

How can large language models assist with a FRAM analysis?

Large Language Models (LLMs) are transforming the way in which people interact with artificial intelligence. In this paper we explore how safety professionals might use LLMs for a FRAM analysis. We use interactive prompting with Google Bard / Gemini and ChatGPT to do a FRAM analysis on examples from healthcare and aviation. Our exploratory findings suggest that LLMs afford safety analysts the opportunity to enhance the FRAM analysis by facilitating initial model generation and offering different perspectives. Responsible and effective utilisation of LLMs requires careful consideration of their limitations as well as their abilities. Human expertise is crucial both with regards to validating the output of the LLM as well as in developing meaningful interactive prompting strategies to take advantage of LLM capabilities such as self-critiquing from different perspectives. Further research is required on effective prompting strategies, and to address ethical concerns

Mercury‐Group 13 Metal Covalent Bonds: A Systematic Comparison of Aluminyl, Gallyl and Indyl Metallo‐ligands

Bimetallic compounds containing direct metal‐group 13 element bonds have been shown to display unprecedented patterns of cooperative reactivity towards small molecules, which can be influenced by the identity of the group 13 element. In this context, we present here a systematic appraisal of group 13 metallo‐ligands of the type [(NON)E]− (NON=4,5‐bis(2,6‐diisopropylanilido)‐2,7‐di‐tert‐butyl‐9,9‐dimethylxanthene) for E=Al, Ga and In, through a comparison of structural and spectroscopic parameters associated with the trans L or X ligands in linear d10 complexes of the types LM{E(NON)} and XM′{E(NON)}. These studies are facilitated by convenient syntheses (from the In(I) precursor, InCp) of the potassium indyl species [{K(NON)In}⋅KCp] n (1) and [(18‐crown‐6)2K2Cp] [(NON)In] (1′), and lead to the first structural characterisation of Ag−In and Hg−E (E=Al, In) covalent bonds. The resulting structural, spectroscopic and quantum chemical probes of Ag/Hg complexes are consistent with markedly stronger σ‐donor capabilities of the aluminyl ligand, [(NON)Al]−, over its gallium and indium counterparts

Reversible [4 + 1] Cycloaddition of Arenes by a “Naked” Acyclic Aluminyl Compound

The large steric profile of the N-heterocyclic boryloxy ligand, –OB­(NDippCH)2, and its ability to stabilize the metal-centered HOMO, are exploited in the synthesis of the first example of a “naked” acyclic aluminyl complex, [K­(2.2.2-crypt)]­[Al­{OB­(NDippCH)2}2]. This system, which is formed by substitution at AlI (rather than reduction of AlIII), represents the first O-ligated aluminyl compound and is shown to be capable of hitherto unprecedented reversible single-site [4 + 1] cycloaddition of benzene. This chemistry and the unusual regioselectivity of the related cycloaddition of anthracene are shown to be highly dependent on the availability (or otherwise) of the K+ countercation

A simple, low-blank batch purification method for high-precision boron isotope analysis

This work was supported by NERC IAPETUS PhD Studentships NE/RO12253/1 to M.T., J.C.B. and E.L., an IAPETUS2 PhD Studentship NE/S007431/1 to C.X.; S.N. was supported by the MOST 111-2116M-002-032-MY3 Grant; J.W.B.R acknowledges support from NERC (Grant NE/N011716/1) and from the European Research Council under the European Union's Horizon 2020 research and innovation program (Grant agreement 805246).Boron (B) isotopes are widely used in the Earth sciences to trace processes ranging from slab recycling in the mantle to changes in ocean pH and atmospheric CO2. Boron isotope analysis is increasingly achieved by multi-collector inductively coupled plasma mass spectrometry, which requires separation of B from the sample matrix. Traditional column chromatography methods for this separation have a well-established track record but are time consuming and prone to contamination from airborne blank. Here, we present an extensive array of tests that establish a novel method for B purification using a batch method. We discuss the key controls and limitations on sample loading, matrix removal and B elution including sample volume, ionic strength, buffer to acid ratio and elution volume, all of which may also help optimize column-based methods. We find consistent, low procedural blanks of 10 ± 16 pg and excellent reproducibility: 10 ng NIST RM 8301 foram [8301f] yields 14.58 ± 0.11‰ 2SD n = 15; 2.5 ng 8301f yields 14.60 ± 0.19‰ 2SD, n = 31; and overall long term 2SD on n = 218 samples pooling different sample sizes yields 14.62 ± 0.21‰ 2SD. This method also offers significant advantages in throughput, allowing the processing of 24 samples in ∼5 hr. This boron batch method thus provides a fast, reproducible, low-blank method for purification of boron for high precision isotopic analyses.Peer reviewe

Nonidet P-40 extraction of lymphocyte plasma membrane. Characterization of the insoluble residue

Purified preparations of lymphocyte plasma membrane were extracted exhaustively with Nonidet P-40 in Dulbecco's phosphate-buffered saline medium. The insoluble fraction, as defined by sedimentation at 10(6) g-min, contained about 10% of the membrane protein as well as cholesterol and phospholipid. The lipid/protein ratio, cholesterol/phospholipid ratio and sphingomyelin content were increased in the residue. Density-gradient centrifugation suggested that the lipid and protein form a common entity. As judged by sodium dodecyl sulphate/polyacrylamide-gel electrophoresis, the Nonidet P-40-insoluble fractions of the plasma membranes of human B lymphoblastoid cells and pig mesenteric lymph-node lymphocytes possessed similar qualitative polypeptide compositions but differed quantitatively. Both residues comprised major polypeptides of Mr 28 000, 33 000, 45 000 and 68 000, together with a prominent band of Mr 120 000 in the human and of Mr 200 000 in the pig. The polypeptides of Mr 28 000, 33 000, 68 000 and 120 000 were probably located exclusively in the Nonidet P-40-insoluble residue, which also possessed a 4-fold increase in 5′-nucleotidase specific activity. The results indicate that a reproducible fraction of lymphocyte plasma membrane is insoluble in non-ionic detergents and that this fraction possesses a unique polypeptide composition. By analogy with similar studies with erythrocyte ghosts, it appears likely that the polypeptides are located on the plasma membrane's cytoplasmic face.</jats:p