4,209 research outputs found
A comparative study of the nonuniqueness problem of the potential equation
The nonuniqueness problem occurring at transonic speeds with the conservative potential equation is investigated numerically. The study indicates that the problem is not an inviscid phenomenon, but results from approximate treatment of shock waves inherent in the conservative potential model. A new bound on the limit of validity of the conservative potential model is proposed
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A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes.
PurposeTo present a detailed, reliable long range-PCR and sequencing (LR-PCR-Seq) procedure to identify human opsin gene sequences for variations in the long wavelength-sensitive (OPN1LW), medium wavelength-sensitive (OPN1MW), short wavelength-sensitive (OPN1SW), and rhodopsin (RHO) genes.MethodsColor vision was assessed for nine subjects using the Farnsworth-Munsell 100 hue test, Ishihara pseudoisochromatic plates, and the Rabin cone-contrast threshold procedure (ColorDX, Konan Medical). The color vision phenotypes were normal trichromacy (n = 3), potential tetrachromacy (n = 3), dichromacy (n = 2), and unexplained low color vision (n = 1). DNA was isolated from blood or saliva and LR-PCR amplified into individual products: OPN1LW (4,045 bp), OPN1MW (4,045 bp), OPN1SW (3,326 bp), and RHO (6,715 bp). Each product was sequenced using specific internal primer sets. Analysis was performed with Mutation Surveyor software.ResultsThe LR-PCR-Seq technique identified known single nucleotide polymorphisms (SNPs) in OPN1LW and OPN1MW gene codons (180, 230, 233, 277, and 285), as well as those for lesser studied codons (174, 178, 236, 274, 279, 298 and 309) in the OPN1LW and OPN1MW genes. Additionally, six SNP variants in the OPN1MW and OPN1LW genes not previously reported in the NCBI dbSNP database were identified. An unreported poly-T region within intron 5(c.36+126) of the rhodopsin gene was also found, and analysis showed it to be highly conserved in mammalian species.ConclusionsThis LR-PCR-Seq procedure (single PCR reaction per gene followed by sequencing) can identify exonic and intronic SNP variants in OPN1LW, OPN1MW, OPN1SW, and rhodopsin genes. There is no need for restriction enzyme digestion or multiple PCR steps that can introduce errors. Future studies will combine the LR-PCR-Seq with perceptual behavior measures, allowing for accurate correlations between opsin genotypes, retinal photopigment phenotypes, and color perception behaviors
Design, development and evaluation of Stanford/Ames Extra-Vehicular Activity (EVA) prehensors
A summary is given of progress to date on work proposed in 1983 and continued in 1985, including design iterations on three different types of manually powered prehensors, construction of functional mockups of each and culminating in detailed drawings and specifications for suit-compatible sealed units for testing under realistic conditions
A brief description of the Jameson-Caughey NYU transonic swept-wing computer program: FLO 22
A computer program for analyzing inviscid, isentropic, transonic flow past 3-D swept configurations is presented. Some basic aspects of the program are: (1) the free-stream Mach number is restricted only by the isentropic assumption; (2) weak shock waves are automatically located wherever they occur in the flow; (3) the finite-difference form of the full equation for the velocity potential is solved by the method of relaxation, after the flow exterior to the airfoil is mapped to the upper half plane; (4) the mapping procedure allows exact satisfaction of the boundary conditions and use of supersonic free stream velocities; (5) the finite difference operator is locally rotated in supersonic flow regions so as to properly account for the domain of dependence; and (6) the relaxation algorithm was stabilized using criteria from a time-like analogy
Biosensor-based engineering of biosynthetic pathways
Biosynthetic pathways provide an enzymatic route from inexpensive renewable resources to valuable metabolic products such as pharmaceuticals and plastics. Designing these pathways is challenging due to the complexities of biology. Advances in the design and construction of genetic variants has enabled billions of cells, each possessing a slightly different metabolic design, to be rapidly generated. However, our ability to measure the quality of these designs lags by several orders of magnitude. Recent research has enabled cells to report their own success in chemical production through the use of genetically encoded biosensors. A new engineering discipline is emerging around the creation and application of biosensors. Biosensors, implemented in selections and screens to identify productive cells, are paving the way for a new era of biotechnological progress
Distributed leadership, trust and online communities
This paper analyses the role of distributed leadership and trust in online communities. The team-based informal ethos of online collaboration requires a different kind of leadership from that in formal positional hierarchies. Such leadership may be more flexible and sophisticated, capable of encompassing ambiguity and rapid change. Online leaders need to be partially invisible, delegating power and distributing tasks. Yet, simultaneously, online communities are facilitated by the high visibility and subtle control of expert leaders. This paradox: that leaders need to be both highly visible and invisible as appropriate, was derived from prior research and tested in the analysis of online community discussions using a pattern-matching process. It is argued that both leader visibility and invisibility are important for the facilitation of trusting collaboration via distributed leadership. Advanced leadership responses to complex situations in online communities foster positive group interaction and decision-making, facilitated through active distribution of specific tasks
WD0837+185:the formation and evolution of an extreme mass ratio white dwarf-brown dwarf binary in Praesepe
There is a striking and unexplained dearth of brown dwarf companions in close
orbits (< 3AU) around stars more massive than the Sun, in stark contrast to the
frequency of stellar and planetary companions. Although rare and relatively
short-lived, these systems leave detectable evolutionary end points in the form
of white dwarf - brown dwarf binaries and these remnants can offer unique
insights into the births and deaths of their parent systems. We present the
discovery of a close (orbital separation ~ 0.006 AU) substellar companion to a
massive white dwarf member of the Praesepe star cluster. Using the cluster age
and the mass of the white dwarf we constrain the mass of the white dwarf
progenitor star to lie in the range 3.5 - 3.7 Msun (B9). The high mass of the
white dwarf means the substellar companion must have been engulfed by the B
star's envelope while it was on the late asymptotic giant branch (AGB). Hence,
the initial separation of the system was ~2 AU, with common envelope evolution
reducing the separation to its current value. The initial and final orbital
separations allow us to constrain the combination of the common envelope
efficiency (alpha) and binding energy parameters (lambda) for the AGB star to
alpha lambda ~3. We examine the various formation scenarios and conclude that
the substellar object was most likely to have been captured by the white dwarf
progenitor early in the life of the cluster, rather than forming in situ.Comment: Accepted for publication in ApJ
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