893 research outputs found
Some neglected axioms in fair division
Conditions one might impose on fair allocation procedures are introduced. Nondiscrimination requires that agents share an item in proportion to their entitlements if they receive nothing else. The "price" procedures of Pratt (2007), including the Nash bargaining procedure, satisfy this. Other prominent efficient procedures do not. In two-agent problems, reducing the feasible set between the solution and one agent's maximum point increases the utility cost to that agent of providing any given utility gain to the other and is equivalent to decreasing the dispersion of the latter's values for the items he does not receive without changing their total. One-agent monotonnicity requires that such a change should not hurt the first agent, limited monotonicity that the solution should not change. For prices, the former implies convexity in the smaller of the two valuations, the latter linearity. In either case, the price is at least their average and hence spiteful.Fair division, efficient allocation, nondiscrimination axiom, monotonicity axioms, envy-free, spite, bargaining solutions.
Personal Pedagogical Systems: Core Beliefs, Foundational Knowledge, and Informal Theories of Teaching
This case study describes a personal pedagogical system that acts a guide for adult educators in their practice. The system reflects core beliefs (assumptions about truth or propriety), foundational knowledge (essential knowledge for effective teaching of adults) and an informal theory of teaching (a theory of what works and what doesn\u27t work), all of which interact dialectically. Implications for further research and practice are discussed
The Ultraviolet Detection of Diffuse Gas in Galaxy Groups
A small survey of the UV-absorbing gas in 12 low- galaxy groups has been
conducted using the Cosmic Origins Spectrograph (COS) on-board the Hubble Space
Telescope (HST). Targets were selected from a large, homogeneously-selected
sample of groups found in the Sloan Digital Sky Survey (SDSS). A critical
selection criterion excluded sight lines that pass close ( virial radii)
to a group galaxy, to ensure absorber association with the group as a whole.
Deeper galaxy redshift observations are used both to search for closer galaxies
and also to characterize these to groups, the
most massive of which are highly-virialized with numerous early-type galaxies
(ETGs). This sample also includes two spiral-rich groups, not yet
fully-virialized. At group-centric impact parameters of 0.3-2 Mpc, these
-30 spectra detected HI absorption in 7 of 12 groups; high
(OVI) and low (SiIII) ion metal lines are present in 2/3 of the absorption
components. None of the three most highly-virialized, ETG-dominated groups are
detected in absorption. Covering fractions % are seen at all impact
parameters probed, but do not require large filling factors despite an enormous
extent. Unlike halo clouds in individual galaxies, group absorbers have radial
velocities which are too low to escape the group potential well without doubt.
This suggests that these groups are "closed boxes" for galactic evolution in
the current epoch. Evidence is presented that the cool and warm group absorbers
are not a pervasive intra-group medium (IGrM), requiring a hotter (
to K) IGrM to be present to close the baryon accounting.Comment: Resubmitted to ApJS after first review; 82 pages (27 for main text,
rest are Appendices and supplemental figures and tables), 47 figures, 21
table
Development and Testing of a High Stability Engine Control (HISTEC) System
Flight tests were recently completed to demonstrate an inlet-distortion-tolerant engine control system. These flight tests were part of NASA's High Stability Engine Control (HISTEC) program. The objective of the HISTEC program was to design, develop, and flight demonstrate an advanced integrated engine control system that uses measurement-based, real-time estimates of inlet airflow distortion to enhance engine stability. With improved stability and tolerance of inlet airflow distortion, future engine designs may benefit from a reduction in design stall-margin requirements and enhanced reliability, with a corresponding increase in performance and decrease in fuel consumption. This paper describes the HISTEC methodology, presents an aircraft test bed description (including HISTEC-specific modifications) and verification and validation ground tests. Additionally, flight test safety considerations, test plan and technique design and approach, and flight operations are addressed. Some illustrative results are presented to demonstrate the type of analysis and results produced from the flight test program
Optimization of chemoenzymatic mass-tagging by strain-promoted cycloaddition (SPAAC) for the determination of O-GlcNAc stoichiometry by Western blotting
The dynamic modification of intracellular proteins by O-linked β-N-acetylglucosamine (O-GlcNAcylation) plays critical roles in many cellular processes. Although various methods have been developed for O-GlcNAc detection, there are few techniques for monitoring glycosylation stoichiometry and state (i.e., mono-, di-, etc., O-GlcNAcylated). Measuring the levels of O-GlcNAcylation on a given substrate protein is important for understanding the biology of this critical modification and for prioritizing substrates for functional studies. One powerful solution to this limitation involves the chemoenzymatic installation of polyethylene glycol polymers of defined molecular mass onto O-GlcNAcylated proteins. These “mass tags” produce shifts in protein migration during sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE) that can be detected by Western blotting. Broad adoption of this method by the scientific community has been limited, however, by a lack of commercially available reagents and well-defined protein standards. Here, we develop a “click chemistry” approach to this method using entirely commercial reagents and confirm the accuracy of the approach using a semisynthetic O-GlcNAcylated protein. Our studies establish a new, expedited experimental workflow and standardized methods that can be readily utilized by non-experts to quantify the O-GlcNAc stoichiometry and state on endogenous proteins in any cell or tissue lysate
A randomized, double-blind, placebo-controlled trial of Ad5FGF-4 gene therapy and its effect on myocardial perfusion in patients with stable angina
AbstractObjectivesThe primary objective of this study was to determine whether intracoronary administration of the adenoviral gene for fibroblast growth factor (Ad5FGF-4) can improve myocardial perfusion compared with placebo.BackgroundAnimal studies and observational clinical studies have shown improvement in perfusion of the ischemic myocardium using genes encoding angiogenic growth factors; however, randomized, double-blind data in humans are lacking.MethodsWe performed a randomized, double-blind, placebo-controlled trial of intracoronary injection of 1010adenoviral particles containing a gene encoding fibroblast growth factor (Ad5FGF-4) to determine the effect on myocardial perfusion. Fifty-two patients with stable angina and reversible ischemia comprising >9% of the left ventricle on adenosine single-photon emission computed tomography (SPECT) imaging were randomized to gene therapy (n = 35) or placebo (n = 17). Clinical follow-up was performed, and 51 (98%) patients underwent a second adenosine SPECT scan after 8 weeks.ResultsOverall (n = 52), the mean total perfusion defect size at baseline was 32.4% of the left ventricle, with 20% reversible ischemia and 12.5% scar. At eight weeks, Ad5FGF-4 injection resulted in a significant reduction of ischemic defect size (4.2% absolute, 21% relative; p < 0.001) and placebo-treated patients had no improvement (p = 0.32). Although the change in reversible perfusion defect size between Ad5FGF-4 and placebo was not significant (4.2% vs. 1.6%, p = 0.14), when a single outlier was excluded a significant difference was observed (4.2% vs. 0.8%, p < 0.05). Ad5FGF-4 was well tolerated and did not result in any permanent adverse sequelae.ConclusionsIntracoronary injection of Ad5FGF-4 showed an encouraging trend for improved myocardial perfusion; however, further studies of therapeutic angiogenesis with Ad5FGF-4 will be necessary
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