4,767 research outputs found

    Abstract Innovation, Virtual Ideas, and Artificial Legal Thought

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    Parity Violating Electron Scattering Measurements of Neutron Densities

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    Parity violating electron scattering allows model independent measurements of neutron densities that are free from most strong interaction uncertainties. In this paper we present statistical error estimates for a variety of experiments. The neutron radius RnR_n can be measured in several nuclei, as long as the nuclear excited states are not too low in energy. We present error estimates for RnR_n measurements in 40^{40}Ca, 48^{48}Ca, 112^{112}Sn, 120^{120}Sn, 124^{124}Sn, and 208^{208}Pb. In general, we find that the smaller the nucleus, the easier the measurement. This is because smaller nuclei can be measured at higher momentum transfers where the parity violating asymmetry ApvA_{pv} is larger. Also in general, the more neutron rich the isotope, the easier the measurement, because neutron rich isotopes have larger weak charges and larger ApvA_{pv}. Measuring RnR_n in 48^{48}Ca appears very promising because it has a higher figure of merit than 208^{208}Pb. In addition, Rn(48R_n(^{48}Ca) may be more easily related to two nucleon and three nucleon interactions, including very interesting three neutron forces, than Rn(208R_n(^{208}Pb). After measuring RnR_n, one can constrain the surface thickness of the neutron density ana_n with a second measurement at somewhat higher momentum transfers. We present statistical error estimates for measuring ana_n in 48^{48}Ca, 120^{120}Sn, and 208^{208}Pb. Again, we find that ana_n is easier to measure in smaller nuclei.Comment: 10 pages, 7 fig., minor changes, J. Phys. G in pres

    Electroweak Measurements of Neutron Densities in CREX and PREX at JLab, USA

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    Measurement of the parity-violating electron scattering asymmetry is an established technique at Jefferson Lab and provides a new opportunity to measure the weak charge distribution and hence pin down the neutron radius in nuclei in a relatively clean and model-independent way. This is because the Z boson of the weak interaction couples primarily to neutrons. We will describe the PREX and CREX experiments on 208{}^{208}Pb and 48{}^{48}Ca respectively; these are both doubly-magic nuclei whose first excited state can be discriminated by the high resolution spectrometers at JLab. The heavier lead nucleus, with a neutron excess, provides an interpretation of the neutron skin thickness in terms of properties of bulk neutron matter. For the lighter 48{}^{48}Ca nucleus, which is also rich in neutrons, microscopic nuclear theory calculations are feasible and are sensitive to poorly constrained 3-neutron forces.Comment: A contribution to the upcoming EPJA Special Volume on Nuclear Symmetry Energ

    Fastow and Arthur Andersen: Some Reflections on Corporate Criminality, Victim Status, and Retribution

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    Spatial control of irreversible protein aggregation

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    Liquid cellular compartments spatially segregate from the cytoplasm and can regulate aberrant protein aggregation, a process linked to several medical conditions, including Alzheimer's and Parkinson's diseases. Yet the mechanisms by which these droplet-like compartments affect protein aggregation remain unknown. Here, we combine kinetic theory of protein aggregation and liquid-liquid phase separation to study the spatial control of irreversible protein aggregation in the presence of liquid compartments. We find that, even for weak interactions between the compartment constituents and the aggregating monomers, aggregates are strongly enriched inside the liquid compartment relative to the surrounding cytoplasm. We show that this enrichment is caused by a positive feedback mechanism of aggregate nucleation and growth which is mediated by a flux maintaining the phase equilibrium between the compartment and the cytoplasm. Our model predicts that the compartment volume that maximizes aggregate enrichment in the compartment is determined by the reaction orders of aggregate nucleation. The underlying mechanism of aggregate enrichment could be used to confine cytotoxic protein aggregates inside droplet-like compartments suggesting potential new avenues against aberrant protein aggregation. Our findings could also represent a common mechanism for the spatial control of irreversible chemical reactions in general

    Low Vision in Older Adults

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    Educational Objectives 1. Understand the epidemiology of visual impairments of older adults. 2. Understand the symptoms of functional loss secondary to visual impairments. 3. Understand the rehabilitative options available for those with vision loss. 4. Understand the multi-disciplinary approach in low vision rehabilitation. 5. Understand the impact of low vision rehabilitation services
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