67 research outputs found

    Recasting Navier–Stokes equations

    Get PDF
    Classical Navier-Stokes equations fail to describe some flows in both the compressible and incompressible configurations. In this article, we propose a new methodology based on transforming the fluid mass velocity vector field to obtain a new class of continuum models. We uncover a class of continuum models which we call the re-casted Navier-Stokes. They naturally exhibit the physics of previously proposed models by different authors to substitute the original Navier-Stokes equations. The new models unlike the conventional Navier-Stokes appear as more complete forms of mass diffusion type continuum flow equations. They also form systematically a class of thermo-mechanically consistent hydrodynamic equations via the original equations. The plane wave analysis is performed to check their linear stability under small perturbations, which confirms that all re-casted models are spatially and temporally stable like their classical counterpart. We then use the Rayleigh-Brillouin scattering experiments to demonstrate that the re-casted equations may be better suited for explaining some of the experimental data where original Navier-Stokes fail

    Consequences of a telomerase-related fitness defect and chromosome substitution technology in yeast synIX strains

    Get PDF
    We describe the complete synthesis, assembly, debugging, and characterization of a synthetic 404,963 bp chromosome, synIX (synthetic chromosome IX). Combined chromosome construction methods were used to synthesize and integrate its left arm (synIXL) into a strain containing previously described synIXR. We identified and resolved a bug affecting expression of EST3, a crucial gene for telomerase function, producing a synIX strain with near wild-type fitness. To facilitate future synthetic chromosome consolidation and increase flexibility of chromosome transfer between distinct strains, we combined chromoduction, a method to transfer a whole chromosome between two strains, with conditional centromere destabilization to substitute a chromosome of interest for its native counterpart. Both steps of this chromosome substitution method were efficient. We observed that wild-type II tended to co-transfer with synIX and was co-destabilized with wild-type IX, suggesting a potential gene dosage compensation relationship between these chromosomes. </p

    The impacts of urban air pollution on Malaysian traffic police: A framework for evaluation of real-time monitoring system on its usability

    Get PDF
    The respiratory health of Malaysian Traffic Police has been compromised by working in heavy traffic and congested junctions with bad air for long hours. A wireless outdoor individual exposure device is vital to track their exposure, however, the efficacy of the system remains uncertain. While existing techniques exist to examine the efficacy of such system, there is a lack of methodology for engaging multiple assessment methods to evaluate the degree of user experience. This paper aims to propose a methodological framework tool for a quantitative evaluation of the wireless outdoor individual exposure indicator system prototype. A systematic search was conducted in major electronic databases (MEDLINE, Web of Science, Google), grey literature sources and all relevant data in the field. A three-stage framework consisting of simulation real-time monitoring, in-field testing, and usability testing is assembled. The three-stage framework proposed serves as a generic approach for evaluating the prototype with the purpose of tracking individual outdoor exposure. The method is capable of describing the complete evaluation process, from the accuracy and performance of the sensor to the extent of the end-user experience. Using the three-stage approach, future researchers may be able to create a monitoring system that is relevant to their needs

    Resistance gene cloning from a wild crop relative by sequence capture and association genetics

    Get PDF
    Disease resistance (R) genes from wild relatives could be used to engineer broad-spectrum resistance in domesticated crops. We combined association genetics with R gene enrichment sequencing (AgRenSeq) to exploit pan-genome variation in wild diploid wheat and rapidly clone four stem rust resistance genes. AgRenSeq enables R gene cloning in any crop that has a diverse germplasm panel

    Rapid cloning of disease-resistance genes in plants using mutagenesis and sequence capture

    Get PDF
    Wild relatives of domesticated crop species harbor multiple, diverse, disease resistance (R) genes that could be used to engineer sustainable disease control. However, breeding R genes into crop lines often requires long breeding timelines of 5–15 years to break linkage between R genes and deleterious alleles (linkage drag). Further, when R genes are bred one at a time into crop lines, the protection that they confer is often overcome within a few seasons by pathogen evolution1. If several cloned R genes were available, it would be possible to pyramid R genes2 in a crop, which might provide more durable resistance1. We describe a three-step method (MutRenSeq)-that combines chemical mutagenesis with exome capture and sequencing for rapid R gene cloning. We applied MutRenSeq to clone stem rust resistance genes Sr22 and Sr45 from hexaploid bread wheat. MutRenSeq can be applied to other commercially relevant crops and their relatives, including, for example, pea, bean, barley, oat, rye, rice and maize
    corecore