82 research outputs found

    The problem of depth in geology: When pressure does not translate into depth

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    We review published evidence that rocks can develop, sustain and record significant pressure deviations from lithostatic values. Spectroscopic studies at room pressure and temperature (P-T) reveal that in situ pressure variations in minerals can reach GPa levels. Rise of confined pressure leads to higher amplitude of these variations documented by the preservation of α-quartz incipiently amorphized under pressure (IAUP quartz), which requires over 12 GPa pressure variations at the grain scale. Formation of coesite in rock-deformation experiments at lower than expected confined pressures confirmed the presence of GPa-level pressure variations at elevated temperatures and pressures within deforming and reacting multi-mineral and polycrystalline rock samples. Whiteschists containing garnet porphyroblasts formed during prograde metamorphism that host quartz inclusions in their cores and coesite inclusions in their rims imply preservation of large differences in pressure at elevated pressure and temperature. Formation and preservation of coherent cryptoperthite exsolution lamellae in natural alkali feldspar provides direct evidence for grain-scale, GPa-level stress variations at 680°C at geologic time scales from peak to ambient P-T conditions. Similarly, but in a more indirect way, the universally accepted' pressure-vessel' model to explain preservation of coesite, diamond and other ultra-high-pressure indicators requires GPa-level pressure differences between the inclusion and the host during decompression at temperatures sufficiently high for these minerals to transform into their lower pressure polymorphs even at laboratory time scales. A variety of mechanisms can explain the formation and preservation of pressure variations at various length scales. These mechanisms may double the pressure value compared to the lithostatic in compressional settings, and pressures up to two times the lithostatic value were estimated under special mechanical conditions. We conclude, based on these considerations, that geodynamic scenarios involving very deep subduction processes with subsequent very rapid exhumation from a great depth must be viewed with due caution when one seeks to explain the presence of microscopic ultrahigh-pressure mineralogical indicators in rocks. Non-lithostatic interpretation of high-pressure indicators may potentially resolve long-lasting geological conundrum

    Ion association in concentrated NaCI brines from ambient to supercritical conditions: results from classical molecular dynamics simulations

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    Highly concentrated NaCl brines are important geothermal fluids; chloride complexation of metals in such brines increases the solubility of minerals and plays a fundamental role in the genesis of hydrothermal ore deposits. There is experimental evidence that the molecular nature of the NaCl–water system changes over the pressure–temperature range of the Earth's crust. A transition of concentrated NaCl–H(2)O brines to a "hydrous molten salt" at high P and T has been argued to stabilize an aqueous fluid phase in the deep crust. In this work, we have done molecular dynamic simulations using classical potentials to determine the nature of concentrated (0.5–16 m) NaCl–water mixtures under ambient (25°C, 1 bar), hydrothermal (325°C, 1 kbar) and deep crustal (625°C, 15 kbar) conditions. We used the well-established SPCE model for water together with the Smith and Dang Lennard-Jones potentials for the ions (J. Chem. Phys., 1994, 100, 3757). With increasing temperature at 1 kbar, the dielectric constant of water decreases to give extensive ion-association and the formation of polyatomic (Na(n)Cl(m))(n-m )clusters in addition to simple NaCl ion pairs. Large polyatomic (Na(n)Cl(m))(n-m )clusters resemble what would be expected in a hydrous NaCl melt in which water and NaCl were completely miscible. Although ion association decreases with pressure, temperatures of 625°C are not enough to overcome pressures of 15 kbar; consequently, there is still enhanced Na–Cl association in brines under deep crustal conditions

    A Functional Misexpression Screen Uncovers a Role for Enabled in Progressive Neurodegeneration

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    Drosophila is a well-established model to study the molecular basis of neurodegenerative diseases. We carried out a misexpression screen to identify genes involved in neurodegeneration examining locomotor behavior in young and aged flies. We hypothesized that a progressive loss of rhythmic activity could reveal novel genes involved in neurodegenerative mechanisms. One of the interesting candidates showing progressive arrhythmicity has reduced enabled (ena) levels. ena down-regulation gave rise to progressive vacuolization in specific regions of the adult brain. Abnormal staining of pre-synaptic markers such as cystein string protein (CSP) suggest that axonal transport could underlie the neurodegeneration observed in the mutant. Reduced ena levels correlated with increased apoptosis, which could be rescued in the presence of p35, a general Caspase inhibitor. Thus, this mutant recapitulates two important features of human neurodegenerative diseases, i.e., vulnerability of certain neuronal populations and progressive degeneration, offering a unique scenario in which to unravel the specific mechanisms in an easily tractable organism

    Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018.

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    Over the past decade, the Nomenclature Committee on Cell Death (NCCD) has formulated guidelines for the definition and interpretation of cell death from morphological, biochemical, and functional perspectives. Since the field continues to expand and novel mechanisms that orchestrate multiple cell death pathways are unveiled, we propose an updated classification of cell death subroutines focusing on mechanistic and essential (as opposed to correlative and dispensable) aspects of the process. As we provide molecularly oriented definitions of terms including intrinsic apoptosis, extrinsic apoptosis, mitochondrial permeability transition (MPT)-driven necrosis, necroptosis, ferroptosis, pyroptosis, parthanatos, entotic cell death, NETotic cell death, lysosome-dependent cell death, autophagy-dependent cell death, immunogenic cell death, cellular senescence, and mitotic catastrophe, we discuss the utility of neologisms that refer to highly specialized instances of these processes. The mission of the NCCD is to provide a widely accepted nomenclature on cell death in support of the continued development of the field
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