686 research outputs found

    High level sill and dyke intrusions initiated from rapidly buried mafic lava flows in scoria cones of Tongoa, Vanuatu (New Hebrides), South Pacific

    Get PDF
    Scoria cones are generally considered to grow rapidly in days to weeks or months. During their growth lava flows may be fed onto the cone surface from lava-lake breaches, or form by coalescence of spatter; such flows are preserved interbedded with scoria lapilli and ash beds. On Tongoa, an island of the Vanuatu volcanic arc in the South Pacific, a series of scoria cones developed during the Holocene, forming a widespread monogenetic volcanic field. Half sections of scoria cones along the coast expose complex interior architecture cone architectures. On the western side of Tongoa Island a scoria cone remnant with steeply crater-ward dipping beds of scoria ash and lapilli contains various dm-to-m thick lava flows, which are connected by irregular dikes cutting obliquely across the beds of the cone. The lava flows are coherent igneous bodies with well-developed flow top and basal breccias. The lavas interbedded with the cone-forming layers are part of a larger (up to 7 m thick) body that is connected to dykes and sills of irregular geometries that intrude the cone's pyroclastic layers. This 3D relationship suggests that the lava flows were buried quickly under the accumulating scoriaceous deposits. This allowed subsequent escape of magma from the fluid interiors of flows, with the magma then squeezed upward or laterally into the accumulating pyroclastic pile. Movement of the pile above the partly mobile lava, and potential destabilisation during intrusion into the pile of lava squeezed from the flows, may signal the onset of localised cone failures, and could be implicated in development of major cone breaches (e.g. Paricutin)

    Compositional variation during monogenetic volcano growth and its implications for magma supply to continental volcanic fields

    Get PDF
    Individual volcanoes of continental monogenetic volcanic fields are generally presumed to erupt single magma batches during brief eruptions. Nevertheless, in two unrelated volcanic fields (the Waipiata volcanic field, New Zealand, and the Miocene-Pliocene volcanic field in western Hungary), we have identified pronounced and systematic compositional differences among products of individual volcanoes. We infer that this indicates a two-stage process of magma supply for these volcanoes. Each volcano records: (1) intrusion of a basanitic parent magma to lower- to mid-crustal levels and its subsequent fractionation to form a tephritic residual melt;, (2) subsequent transection of this reservoir by a second batch of basanitic melt, with tephrite rising to the surface at the head of the propagating basanite dyke. Eruption at the surface then yields initial tephrite, typically erupted as pyroclasts, followed by eruption and shallow intrusion of basanite from deeper in the dyke. By analogy with similar tephrite-basanite eruptions along rift zones of intraplate ocean-island volcanoes, we infer that fractionation to tephrite would have required decades to centuries. We conclude that the two studied continental monogenetic volcanic fields demonstrate a consistent history of early magmatic injections that fail to reach the surface, followed by capture and partial eruption of their evolved residues in the course of separate and significantly later injections of basanite that extend to the surface and erupt. This systematic behaviour probably reflects the difficulty of bringing small volumes of dense, primitive magma to the surface from mantle source regions. Ascent through continental crust is aided by the presence in the dyke head of buoyant tephrite captured during transection of the earlier-emplaced melt bodies

    High energy and high power primary Li-CFx_x batteries enabled by the combined effects of the binder and the electrolyte

    Full text link
    Several effective methods have been developed recently to demonstrate simultaneous high energy and high power density in Li - carbon fluoride (CFx_x) batteries. These methods can achieve as high as 1000 Wh/kg energy density at 60-70 kW/kg power density (40-50 C rate) in coin cells and 750 Wh/kg energy density at 12.5 kW/kg power density (20 C rate) in pouch cells. This performance is made possible by ingenious nano-architecture design, controlled porosity, boron doping and electrolyte additives. In the present study, we show that a similarly great performance, 931 Wh/kg energy density at 59 kW/kg power density, can be achieved by using a polyacrylonitrile binder and a LiBF4 electrolyte in Li - graphite fluoride coin cells. We also demonstrate that the observed effect is the result of the right combination of the binder and the electrolyte. We propose that the mechanistic origin of the observed phenomena is an electro-catalytic effect by the polyacrylonitrile binder. While our proposed method has a competitive performance, it also offers a simple implementation and a scalable production of high energy and high power primary Li-CFx_x cells.Comment: 13 pages, 8 figures, 1 tabl

    Fast Methods for Jackknifing Inequality Indices

    Full text link
    The jackknife is a resampling method that uses subsets of the original database by leaving out one observation at a time from the sample. The paper outlines a procedure to obtain jackknife estimates for several inequality indices with only a few passes through the data. The number of passes is independent of the number of observations. Hence, the method provides an efficient way to obtain standard errors of the estimators even if sample size is large. We apply our method using micro data on individual incomes for Germany and the US

    Changes in children’s cognitive development at the Start of School in England 2001–2008.

    Get PDF
    Since 1997, England has seen massive changes in the Early Years including the introduction of an early childhood curriculum, free pre-school education for three-year-olds and local programmes for disadvantaged communities. Many of these initiatives took time to introduce and become established. Beginning in 2001, and each year thereafter until 2008, the authors collected consistent data from thousands of children when they started school at the age of four on a range of variables, chosen because they are good predictors of later success. These included vocabulary, early reading and early mathematics. Children from the same set of 472 state primary schools in England were assessed each year. This paper contributes to the existing studies of educational trends over time by examining the extent to which children's scores on these measures changed over that period; in general, they were found to have remained stable

    Powerful Inhibition of Experimental Human Pancreatic Cancers by Receptor Targeted Cytotoxic LH-RH analog AEZS-108

    Get PDF
    Pancreatic carcinoma is one of the cancers with the worse prognosis, thus any therapeutic improvement is imperative. Cytotoxic LH-RH analog, AN-152 (proprietary designation, AEZS-108), consisting of doxorubicin (DOX) conjugated to D-Lys6LH-RH, is now in clinical trials for targeted therapy of several sex hormone-dependent tumors that express LH-RH receptors. We investigated LH-RH receptors in human pancreatic carcinoma and the effects of AN-152 (AEZS-108) on experimental pancreatic cancers. We determined LH-RH receptor presence in human pancreatic cancer samples by immunohistochemistry and, in three human pancreatic cancer lines (SW-1990, Panc-1 and CFPAC-1), by binding assays and Western blotting. The effects of the cytotoxic LH-RH analog were investigated on growth of these same cancer lines xenografted into nude mice. We also analyzed differences between the antitumor effects of the cytotoxic analog and its cytotoxic radical alone, doxorubicin (DOX), on the expression of cancer-related genes by PCR arrays. LH-RH receptors were expressed in two randomly selected surgically removed human pancreatic cancer samples and in all three cancer lines. Cytotoxic LH-RH analogs powerfully inhibited growth of all three tumor lines in nude mice; AN-152 was significantly stronger than DOX on Panc-1 and CFPAC-1 cancers. PCR array showed that cytotoxic LH-RH analog AN-152 affected the expression of genes associated with cellular migration, invasion, metastasis and angiogenesis more favorably than DOX, however the changes in gene expression varied considerably among the three cancer lines. Cytotoxic LH-RH analog, AEZS-108, may be a useful agent for the treatment of LH-RH receptor positive advanced pancreatic carcinoma

    The organization of the transcriptional network in specific neuronal classes

    Get PDF
    Genome-wide expression profiling has aided the understanding of the molecular basis of neuronal diversity, but achieving broad functional insight remains a considerable challenge. Here, we perform the first systems-level analysis of microarray data from single neuronal populations using weighted gene co-expression network analysis to examine how neuronal transcriptome organization relates to neuronal function and diversity. We systematically validate network predictions using published proteomic and genomic data. Several network modules of co-expressed genes correspond to interneuron development programs, in which the hub genes are known to be critical for interneuron specification. Other co-expression modules relate to fundamental cellular functions, such as energy production, firing rate, trafficking, and synapses, suggesting that fundamental aspects of neuronal diversity are produced by quantitative variation in basic metabolic processes. We identify two transcriptionally distinct mitochondrial modules and demonstrate that one corresponds to mitochondria enriched in neuronal processes and synapses, whereas the other represents a population restricted to the soma. Finally, we show that galectin-1 is a new interneuron marker, and we validate network predictions in vivo using Rgs4 and Dlx1/2 knockout mice. These analyses provide a basis for understanding how specific aspects of neuronal phenotypic diversity are organized at the transcriptional level
    corecore