The Formation of Alluvial Platinum-Group Minerals: Present Knowledge and the Way Ahead

The weathering of platinum-group element (PGE) deposits presents unusual problems, especially in the very active environment of lateritic weathering under tropical conditions. There is clear evidence of the destruction of platinum-group minerals (PGM) to form PGE oxides, or fine intergrowths between relict PGM and iron oxides or hydroxides, as an intermediate stage during weathering. The PGE released by weathering are transported in solution with the more soluble Pd species remaining in solution and travelling further than the less soluble Pt species. The presence of PGM in the laterite differing in mineralogy, mineral assemblage and size from those in the primary rock is difficult to explain, especially when they show secondary textures. Differing interpretations have created controversy. Are alluvial PGM derived unaltered from the primary rock where they are rare and, therefore, not encountered by standard petrographic examination? Is it possible that they could have developed in the laterite by some process that we do not yet fully understand? Some favourable genetic conditions have been outlined and debated. For more than 100 years authors have reported secondary ore textures and recently proposed a biogenic origin. Frank Reith and his co-workers provided evidence of a process involving metallophillic bacteria which, for the first time, demonstrates PGM growth in the laboratory under supergene conditions. Their work shows that a mechanism for supergene growth ('neoformation') can occur, which offers a new field of study of the appropriate Eh, pH, f(O2) conditions and organic and bacterial reactions that could permit supergene growth.Funding from Golden Prospect Mining Company in the UK, and the assistance of the late Prof. H.M. Prichard and Dr M.T. Jackson of Cardiff University. SSB received generous funding from the Department of Education, Universities and Research of the Basque Government (Refs. BFI-2011-254, IT762-13)

Stochastic Interpolation of Precipitation Data From Multiple Sensors

Introduction: This report summarizes the work conducted under Grant No. ECE-8419189, Stochastic Interpolation of Precipitation Data from Multiple Sensors, which was awarded to Utah State University in September, 1985, and completed February 29, 1988. it also covers work under a supplemental award made in February, 1986. The final report is organized into four sections. The following section presents the objective of the research and a brief problem statment. Section 3 contains a summary of second-year work including the project team, work plan, work completed, and publications. In Section4, project conclusions are summarized. A summary of on-going future work is given in Section 5, together with our plans for publication of research results from this project. Copies of preliminary draft manuscripts and completed technical reports which have been prepared as a result of second-year activities are contained in the Appendices. A cummulative summary of project publications is presented in Appendix A

Viral Endomyocardial Infection Is an Independent Predictor and Potentially Treatable Risk Factor for Graft Loss and Coronary Vasculopathy in Pediatric Cardiac Transplant Recipients

ObjectivesThis study sought to evaluate the outcome and prevalence of viral endomyocardial infection after cardiac transplantation.BackgroundViral myocardial infection causes heart failure, but its role after cardiac transplantation is unclear. We hypothesized that viral infection of the cardiac allograft reduces graft survival.MethodsBetween June 1999 and November 2004, 94 pediatric cardiac transplant patients were screened for the presence of viral genome in serial endomyocardial biopsies (EMBs) using polymerase chain reaction (PCR) assays. Graft loss, advanced transplant coronary artery disease (TCAD), and acute rejection (AR) were compared in the PCR-positive (n = 37) and PCR-negative (n = 57) groups, using time-dependent Kaplan-Meier and Cox regression analyses. From November 2002 to November 2004, intravenous immunoglobulin therapy (IVIG) was administered to patients with PCR-positive EMBs. The outcomes of the IVIG-treated, PCR-positive patients (n = 20) were compared with IVIG-untreated, PCR-positive patients (n = 17).ResultsViral genomes were detected in EMBs from 37 (39%) patients; parvovirus B19, adenovirus, and Epstein-Barr virus (EBV) were the most common. The PCR-positive group (n = 37, 25% graft loss at 2.4 years) had decreased graft survival (p < 0.001) compared with the PCR-negative group (n = 57, 25% graft loss at 8.7 years) and developed advanced TCAD prematurely (p = 0.001). The number of AR episodes was similar in both groups. On multivariate analysis, presence of viral genome was an independent risk factor for graft loss (relative risk: 4.2, p = 0.015). The time to advanced TCAD after becoming PCR-positive was longer in the IVIG-treated patients (p = 0.03) with a trend toward improved graft survival (p = 0.06).ConclusionsViral endomyocardial infection is an independent predictor of graft loss in pediatric cardiac transplant recipients. This effect appears to be mediated through premature development of advanced TCAD. IVIG therapy in this subgroup may improve survival and merits further investigation

The Exomars Climate Sounder (EMCS) Investigation

The ExoMars Climate Sounder (EMCS) investigation is developed at the Jet Propulsion Laboratory (Principal Investigator J. T. Schofield) in collaboration with an international scientific team from France, the United Kingdom and the USA. EMCS plans to map daily, global, pole-to-pole profiles of temperature, dust, water and CO2 ices, and water vapor from the proposed 2016 ExoMars Trace Gas Orbiter (EMTGO). These profiles are to be assimilated into Mars General Circulation Models (MGCMs) to generate global, interpolated fields of measured and derived parameters such as wind

The BNO-LNGS joint measurement of the solar neutrino capture rate in 71Ga

We describe a cooperative measurement of the capture rate of solar neutrinos by the reaction 71Ga(\nu_e,e^-)71Ge. Extractions were made from a portion of the gallium target in the Russian-American Gallium Experiment SAGE and the extraction samples were transported to the Gran Sasso laboratory for synthesis and counting at the Gallium Neutrino Observatory GNO. Six extractions of this type were made and the resultant solar neutrino capture rate was 64 ^{+24}_{-22} SNU, which agrees well with the overall result of the gallium experiments. The major purpose of this experiment was to make it possible for SAGE to continue their regular schedule of monthly solar neutrino extractions without interruption while a separate experiment was underway to measure the response of 71Ga to neutrinos from an 37Ar source. As side benefits, this experiment proved the feasibility of long-distance sample transport in ultralow background radiochemical experiments and familiarized each group with the methods and techniques of the other.Comment: 7 pages, no figures; minor additions in version

Physics at a Fermilab Proton Driver

This report documents the physics case for building a 2 MW, 8 GeV superconducting linac proton driver at Fermilab.Comment: 52 pages, 15 figure

A Comprehensive Resource for Induced Pluripotent Stem Cells from Patients with Primary Tauopathies.

Primary tauopathies are characterized neuropathologically by inclusions containing abnormal forms of the microtubule-associated protein tau (MAPT) and clinically by diverse neuropsychiatric, cognitive, and motor impairments. Autosomal dominant mutations in the MAPT gene cause heterogeneous forms of frontotemporal lobar degeneration with tauopathy (FTLD-Tau). Common and rare variants in the MAPT gene increase the risk for sporadic FTLD-Tau, including progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD). We generated a collection of fibroblasts from 140 MAPT mutation/risk variant carriers, PSP, CBD, and cognitively normal controls; 31 induced pluripotent stem cell (iPSC) lines from MAPT mutation carriers, non-carrier family members, and autopsy-confirmed PSP patients; 33 genome engineered iPSCs that were corrected or mutagenized; and forebrain neural progenitor cells (NPCs). Here, we present a resource of fibroblasts, iPSCs, and NPCs with comprehensive clinical histories that can be accessed by the scientific community for disease modeling and development of novel therapeutics for tauopathies