176 research outputs found

    The Effects of Competition on Variation in the Quality and Cost of Medical Care

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    We estimate the effects of hospital competition on the level of and the variation in quality of care and hospital expenditures for elderly Medicare beneficiaries with heart attack. We compare competition's effects on more-severely ill patients, whom we assume value quality more highly, to the effects on less-severely ill, low-valuation patients. We find that low-valuation patients in less-competitive markets receive more intensive treatment than in more-competitive markets, but have statistically similar health outcomes. In contrast, high-valuation patients in less-competitive markets receive less intensive treatment than in more-competitive markets, and have significantly worse health outcomes. Since this competition-induced increase in variation in expenditures is, on net, expenditure-decreasing and outcome-beneficial, we conclude that it is welfare-enhancing. These findings are inconsistent with conventional models of vertical differentiation, although they can be accommodated by more recent models.

    Diffusive-like Redistribution in State-changing Collisions between Rydberg Atoms and Ground State Atoms

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    We report on the study of state-changing collisions between Rydberg atoms and ground state atoms. We employ high-resolution momentum spectroscopy to identify the final states. In contrast to previous studies, we find that the outcome of such collisions is not limited to a single hydrogenic manifold. We observe a redistribution of population over a wide range of final states. We also find that even the decay to states with the same ll as the initial state, but different principal quantum number nn is possible. We model the underlying physical process in the framework of a short-lived Rydberg quasi-molecular complex, where a charge exchange process gives rise to an oscillating electric field that causes transitions within the Rydberg manifold. The distribution of final states shows a diffusive-like behavior

    Chemical differentiation in regions of high-mass star formation I. CS, dust and N2H^+ in southern sources

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    Aims. Our goals are to compare the CS, N2H+ and dust distributions in a representative sample of high-mass star forming dense cores and to determine the physical and chemical properties of these cores. Methods. We compare the results of CS(5-4) and 1.2 mm continuum mapping of twelve dense cores from the southern hemisphere presented in this work, in combination with our previous N2H+(1-0) and CS(2-1) data. We use numerical modeling of molecular excitation to estimate physical parameters of the cores. Results. Most of the maps have several emission peaks (clumps). We derive basic physical parameters of the clumps and estimate CS and N2H+ abundances. Masses calculated from LVG densities are higher than CS virial masses and masses derived from continuum data, implying small-scale clumpiness of the cores. For most of the objects, the CS and continuum peaks are close to the IRAS point source positions. The CS(5-4) intensities correlate with continuum fluxes per beam in all cases, but only in five cases with the N2H+(1-0) intensities. The study of spatial variations of molecular integrated intensity ratios to continuum fluxes reveals that I(N2H+)/F{1.2} ratios drop towards the CS peaks for most of the sources, which can be due to a N2H+ abundance decrease. For CS(5-4), the I(CS)/F{1.2} ratios show no clear trends with distance from the CS peaks, while for CS(2-1) such ratios drop towards these peaks. Possible explanations of these results are considered. The analysis of normalized velocity differences between CS and N2H+ lines has not revealed indications of systematic motions towards CS peaks.Comment: 13 pages, 5 figures, accepted by Astronomy and Astrophysic

    Water and methanol in low-mass protostellar outflows: gas-phase synthesis, ice sputtering and destruction

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    Water in outflows from protostars originates either as a result of gas-phase synthesis from atomic oxygen at T ≳ 200 K, or from sputtered ice mantles containing water ice. We aim to quantify the contribution of the two mechanisms that lead to water in outflows, by comparing observations of gas-phase water to methanol (a grain surface product) towards three low-mass protostars in NGC 1333. In doing so, we also quantify the amount of methanol destroyed in outflows. To do this, we make use of James Clerk Maxwell Telescope and Herschel-Heterodyne Instrument for the Far-Infrared data of H2O, CH3OH and CO emission lines and compare them to RADEX non-local thermodynamic equilibrium excitation simulations. We find up to one order of magnitude decrease in the column density ratio of CH3OH over H2O as the velocity increases in the line wings up to ∼15 km s−1. An independent decrease in X(CH3OH) with respect to CO of up to one order of magnitude is also found in these objects. We conclude that gas-phase formation of H2O must be active at high velocities (above 10 km s−1 relative to the source velocity) to re-form the water destroyed during sputtering. In addition, the transition from sputtered water at low velocities to form water at high velocities must be gradual. We place an upper limit of two orders of magnitude on the destruction of methanol by sputtering effects

    Astrochemistry in an Ion Storage Ring

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    Storage ring studies of low energy electron collisions with molecular ions have been carried out for dissociative recombination (DR) of fluorine-bearing molecules. Here we report on work aiming to improve the understanding of astrochemistry involving HF, a possible spectroscopic tracer of interstellar H2. For CF+ the rate coefficient was obtained for temperatures down to 10 K. For D2F+ the DR fragmentation branching ratios were determined to be 66(3)%, 24(2)%, and 10(2)% for the F+D+D, DF+D, and D2+F channels, respectively. The molecular DR products of this reaction, DF and D2, display an unusually high level of internal excitation, close to their dissociation limit

    Translating potential improvement in the precision and accuracy of lung nodule measurements on computed tomography scans by software derived from artificial intelligence into impact on clinical practice:a simulation study

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    Objectives Accurate measurement of lung nodules is pivotal to lung cancer detection and management. Nodule size forms the main basis of risk categorisation in existing guidelines. However, measurements can be highly variable between manual readers. This paper explores the impact of potentially improved nodule size measurement assisted by generic artificial intelligence (AI)-derived software on clinical management compared with manual measurement. Methods The simulation study created a baseline cohort of people with lung nodules, guided by nodule size distributions reported in the literature. Precision and accuracy were simulated to emulate measurement of nodule size by radiologists with and without the assistance of AI-derived software and by the software alone. Nodule growth was modelled over a 4-year time frame, allowing evaluation of management strategies based on existing clinical guidelines. Results Measurement assisted by AI-derived software increased cancer detection compared to an unassisted radiologist for a combined solid and sub-solid nodule population (62.5% vs 61.4%). AI-assisted measurement also correctly identified more benign nodules (95.8% vs 95.4%), however it was associated with over an additional month of surveillance on average (5.12 vs 3.95 months). On average, with AI assistance people with cancer are diagnosed faster, and people without cancer are monitored longer. Conclusions In this simulation, the potential benefits of improved accuracy and precision associated with AI-based diameter measurement is associated with additional monitoring of non-cancerous nodules. AI may offer additional benefits not captured in this simulation, and it is important to generate data supporting these, and adjust guidelines as necessary. Advances in Knowledge This paper shows the effects of greater measurement accuracy associated with AI assistance compared with unassisted measurement

    Microkinetic Analysis of the Oxygen Evolution Performance at Different Stages of Iridium Oxide Degradation

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    The microkinetics of the electrocatalytic oxygen evolution reaction substantially determines the performance in proton-exchange membrane water electrolysis. State-of-the-art nanoparticulated rutile IrO2_{2} electrocatalysts present an excellent trade-off between activity and stability due to the efficient formation of intermediate surface species. To reveal and analyze the interaction of individual surface processes, a detailed dynamic microkinetic model approach is established and validated using cyclic voltammetry. We show that the interaction of three different processes, which are the adsorption of water, one potential-driven deprotonation step, and the detachment of oxygen, limits the overall reaction turnover. During the reaction, the active IrO2_{2} surface is covered mainly by *O, *OOH, and *OO adsorbed species with a share dependent on the applied potential and of 44, 28, and 20% at an overpotential of 350 mV, respectively. In contrast to state-of-the-art calculations of ideal catalyst surfaces, this novel model-based methodology allows for experimental identification of the microkinetics as well as thermodynamic energy values of real pristine and degraded nanoparticles. We show that the loss in electrocatalytic activity during degradation is correlated to an increase in the activation energy of deprotonation processes, whereas reaction energies were marginally affected. As the effect of electrolyte-related parameters does not cause such a decrease, the model-based analysis demonstrates that material changes trigger the performance loss. These insights into the degradation of IrO2_{2} and its effect on the surface processes provide the basis for a deeper understanding of degrading active sites for the optimization of the oxygen evolution performance

    Phase- and Surface Composition-Dependent Electrochemical Stability of Ir-Ru Nanoparticles during Oxygen Evolution Reaction

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    The increasing scarcity of iridium (Ir) and its rutile-type oxide (IrO2_{2}), the current state-of-the-art oxygen evolution reaction (OER) catalysts, is driving the transition toward the use of mixed Ir oxides with a highly active yet inexpensive metal (Irx_{x}M1x_{1-x}O2_{2}). Ruthenium (Ru) has been commonly employed due to its high OER activity although its electrochemical stability in Ir-Ru mixed oxide nanoparticles (Irx_{x}Ru1x_{1-x}O2_{2} NPs), especially at high relative contents, is rarely evaluated for long-term application as water electrolyzers. In this work, we bridge the knowledge gap by performing a thorough study on the composition- and phase-dependent stability of well-defined Irx_{x}Ru1x_{1-x}O2_{2} NPs prepared by flame spray pyrolysis under dynamic operating conditions. As-prepared NPs (Irx_{x}Ru1x_{1-x}Oy_{y}) present an amorphous coral-like structure with a hydrous Ir-Ru oxide phase, which upon post-synthetic thermal treatment fully converts to a rutile-type structure followed by a selective Ir enrichment at the NP topmost surface. It was demonstrated that Ir incorporation into a RuO2_{2} matrix drastically reduced Ru dissolution by ca. 10-fold at the expense of worsening Ir inherent stability, regardless of the oxide phase present. Hydrous Irx_{x}Ru1x_{1-x}Oy_{y} NPs, however, were shown to be 1000-fold less stable than rutile-type Irx_{x}Ru1x_{1-x}O2_{2}, where the severe Ru leaching yielded a fast convergence toward the activity of monometallic hydrous IrOy_{y}. For rutile-type Irx_{x}Ru1x_{1-x}O2_{2}, the sequential start-up/shut-down OER protocol employed revealed a steady-state dissolution for both Ir and Ru, as well as the key role of surface Ru species in OER activity: minimal Ru surface losses (<1 at. %) yielded OER activities for tested Ir0.2_{0.2}Ru0.8_{0.8}O2 equivalent to those of untested Ir0.8_{0.8}Ru0.2_{0.2}O2. Ir enrichment at the NP topmost surface, which mitigates selective subsurface Ru dissolution, is identified as the origin of the NP stabilization. These results suggest Ru-rich Irx_{x}Ru1x_{1-x}O2_{2} NPs to be viable electrocatalysts for long-term water electrolysis, with significant repercussions in cost reduction

    Continent-wide decoupling of Y-chromosomal genetic variation from language and geography in native South Americans

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    Numerous studies of human populations in Europe and Asia have revealed a concordance between their extant genetic structure and the prevailing regional pattern of geography and language. For native South Americans, however, such evidence has been lacking so far. Therefore, we examined the relationship between Y-chromosomal genotype on the one hand, and male geographic origin and linguistic affiliation on the other, in the largest study of South American natives to date in terms of sampled individuals and populations. A total of 1,011 individuals, representing 50 tribal populations from 81 settlements, were genotyped for up to 17 short tandem repeat (STR) markers and 16 single nucleotide polymorphisms (Y-SNPs), the latter resolving phylogenetic lineages Q and C. Virtually no structure became apparent for the extant Y-chromosomal genetic variation of South American males that could sensibly be related to their inter-tribal geographic and linguistic relationships. This continent-wide decoupling is consistent with a rapid peopling of the continent followed by long periods of isolation in small groups. Furthermore, for the first time, we identified a distinct geographical cluster of Y-SNP lineages C-M217 (C3*) in South America. Such haplotypes are virtually absent from North and Central America, but occur at high frequency in Asia. Together with the locally confined Y-STR autocorrelation observed in our study as a whole, the available data therefore suggest a late introduction of C3* into South America no more than 6,000 years ago, perhaps via coastal or trans-Pacific routes. Extensive simulations revealed that the observed lack of haplogroup C3* among extant North and Central American natives is only compatible with low levels of migration between the ancestor populations of C3* carriers and non-carriers. In summary, our data highlight the fact that a pronounced correlation between genetic and geographic/cultural structure can only be expected under very specific conditions, most of which are likely not to have been met by the ancestors of native South Americans
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