Age of Obsidian Butte in Imperial County, California, through infrared stimulated luminescence dating of Potassium Feldspar from tuffaceous sediment

Obsidian Butte is an important lithic source for obsidian and artifacts from this location are distributed across archaeological sites in southern California and adjacent parts of northern Mexico. For this study, we used drill core material for infrared stimulated luminescence (IRSL) dating of potassium feldspar extracted from tuffaceous sediment directly underlying obsidian-bearing lava from Obsidian Butte. In addition, a core sample from lacustrine sediment below the tuffaceous sedimentary unit was dated by the same method. Stratigraphically consistent ages between 2.51 ± 0.32 kilo-annum (ka) (1 sigma uncertainty; average of two tuffaceous sediment samples) and 4.39 ± 0.49 ka (lacustrine sediment sample) were obtained. This constrains the eruption and earliest availability of the lithic resource of Obsidian Butte to 490 BCE (with uncertainty limits of ±320 years at ∼68 percent confidence, and ±640 years at ∼95 percent confidence). Since then, it would have been accessible during intermittent desiccation of Lake Cahuilla. This new date redefines obsidian from Obsidian Butte as a marker for the late prehistoric period

Magnetism in Dense Quark Matter

We review the mechanisms via which an external magnetic field can affect the ground state of cold and dense quark matter. In the absence of a magnetic field, at asymptotically high densities, cold quark matter is in the Color-Flavor-Locked (CFL) phase of color superconductivity characterized by three scales: the superconducting gap, the gluon Meissner mass, and the baryonic chemical potential. When an applied magnetic field becomes comparable with each of these scales, new phases and/or condensates may emerge. They include the magnetic CFL (MCFL) phase that becomes relevant for fields of the order of the gap scale; the paramagnetic CFL, important when the field is of the order of the Meissner mass, and a spin-one condensate associated to the magnetic moment of the Cooper pairs, significant at fields of the order of the chemical potential. We discuss the equation of state (EoS) of MCFL matter for a large range of field values and consider possible applications of the magnetic effects on dense quark matter to the astrophysics of compact stars.Comment: To appear in Lect. Notes Phys. "Strongly interacting matter in magnetic fields" (Springer), edited by D. Kharzeev, K. Landsteiner, A. Schmitt, H.-U. Ye

Precise Determination of Proton Spin-Precession Angles in the K600 Spectrometer and Beamline

This research was sponsored by the National Science Foundation Grant NSF PHY-931478

A Complete Set of In-plane Spin-transfer Coefficients for Small Angle pp Elastic Scattering at 200 MeV

This research was sponsored by the National Science Foundation Grant NSF PHY-931478

Possible Observation of the 1/2+ [880] Orbital in 249-Cm

This research was sponsored by the National Science Foundation Grant NSF PHY-931478

Medium Effects in the Normal Component Polarization Observables for the 13-C(p,p')13-C, (1/2)- → (9/2)+ Reaction at 200 MeV

This research was sponsored by the National Science Foundation Grant NSF PHY-931478

Proton Unbound States in T=3/2 and T=2 Nuclei and the Reaction Rates for Sequential Two-proton Capture Reactions in the rp-Process

This research was sponsored by the National Science Foundation Grant NSF PHY-931478

Specific MRI abnormalities reveal severe perrault syndrome due to CLPP defects

In establishing a genetic diagnosis in heterogeneous neurological disease, clinical characterization and whole exome sequencing (WES) go hand-in-hand. Clinical data are essential, not only to guide WES variant selection and define the clinical severity of a genetic defect but also to identify other patients with defects in the same gene. In an infant patient with sensorineural hearing loss, psychomotor retardation, and epilepsy, WES resulted in identification of a novel homozygous CLPP frameshift mutation (c.21delA). Based on the gene defect and clinical symptoms, the diagnosis Perrault syndrome type 3 (PRLTS3) was established. The patient's brain-MRI revealed specific abnormalities of the subcortical and deep cerebral white matter and the middle blade of the corpus callosum, which was used to identify similar patients in the Amsterdam brain-MRI database, containing over 3000 unclassified leukoencephalopathy cases. In three unrelated patients with similar MRI abnormalities the CLPP gene was sequenced, and in two of them novel missense mutations were identified together with a large deletion that covered part of the CLPP gene on the other allele. The severe neurological and MRI abnormalities in these young patients were due to the drastic impact of the CLPP mutations, correlating with the variation in clinical manifestations among previously reported patients. Our data show that similarity in brain-MRI patterns can be used to identify novel PRLTS3 patients, especially during early disease stages, when only part of the disease manifestations are present. This seems especially applicable to the severely affected cases in which CLPP function is drastically affected and MRI abnormalities are pronounced