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These data contain time series of stress, strain, confining pressure, pore pressure, pore volume, permeability and elastic wave velocities of samples of Purbeck Limestone deformed under hydrostatic and triaxial conditions at room temperature. All samples were saturated with decane as pore fluid.This dataset is used and fully described/interpreted in the paper: Brantut, N., M. Baker, L. N. Hansen and P. Baud, Microstructural control of physical properties during deformation of porous limestone, submitted to J. Geophys. Res.
Data output from the numerical flow modelling in GRL manuscript ""Evidence for the top-down control of lava domes on magma ascent dynamics"", by Marsden, L., Neuberg, J. & Thomas, M., all of University of Leeds. The models were created using the Laminar Flow module in COMSOL Multiphysics v5.4 by L. Marsden. The following files are uploaded: Archive_Reference_Model.txt (Reference flow model: Gas loss function, Initial H2O content = 4.5 wt.% Excess pressure at depth = 10 MPa, Constant corresponding to crystal growth rate = 4e-6 s^-1 ) Archive_High_H2O.txt (Gas loss function, Initial H2O content = 10 wt.% Excess pressure at depth = 10 MPa, Constant corresponding to crystal growth rate = 4e-6 s^-1) Archive_No_Gas_Loss.txt (No gas loss, Initial H2O content = 4.5 wt.% Excess pressure at depth = 10 MPa, Constant corresponding to crystal growth rate = 4e-6 s^-1) Archive_Gamma_Low.txt (Gas loss function, Initial H2O content = 4.5 wt.% Excess pressure at depth = 10 MPa, Constant corresponding to crystal growth rate = 1e-6 s^-1) Archive_Excess_Pressure_0MPa.txt (Gas loss function, Initial H2O content = 4.5 wt.% Excess pressure at depth = 0 MPa, Constant corresponding to crystal growth rate = 4e-6 s^-1) Archive_Excess_Pressure_20MPa.txt (Gas loss function, Initial H2O content = 4.5 wt.% Excess pressure at depth = 20 MPa, Constant corresponding to crystal growth rate = 4e-6 s^-1) The files uploaded include the reference flow model and where a single key parameter has been changed in the flow modelling. We include data where the key parameter is at the upper or lower limit of the values tested. Data are not included where magma ascent is modelled to stall without the extrusion of a lava dome, as a time dependent model is not run in this case. A solution is provided using equilibrium modelling only. The following variables are output, at conduit centre unless specified: Depth (m), Time(s), Ascent velocity (m/s), Bulk Viscosity (Pa s), Crystal Content, Dome height (m), Gas Volume Fraction, Overpressure (Pa), Shear Stress at Conduit Wall (Pa)
Data produced from NERC Grant NE/J008745/1. Grant Abstract: Iron sulfides are widespread in the environment, where they regulate and control the global geochemical iron and sulfur cycles. However, despite their application as indicators for seawater anoxia and recorders of early-life isotopic and paleomagnetic data, iron sulfide minerals are still largely unexplored compared to, for example, iron oxide minerals or the silicates or carbonates. Numerous iron sulfide phases are known, but many are highly unstable or only partially stable for a short time in the environment. Even the least reactive iron sulfide, pyrite, is no longer stable once exposed to air at the Earth's surface. Its dissolution leads to the problem of acid mine drainage, where sulfuric acid and any trapped toxic metals are released with devastating effects on the environment near the mine. However, iron sulfides also have beneficial effects on the environment, as they easily incorporate metals within their structure, and thus could be sinks for toxic metals or radioactive elements. An intriguing aspect of iron sulfides is the crucial role they may have played in the Origin of Life. Thin layers of iron-nickel sulfide are believed to have formed in the warm, alkaline springs on the bottom of the oceans on Early Earth. They are increasingly considered to have been the early catalysts for a series of chemical reactions leading to the emergence of life. The oxygen-free production of various organic compounds, including amino acids and nucleic acid bases - the building blocks of DNA - is thought to have been catalyzed by small iron-nickel-sulfur clusters, which are structurally similar to the highly reactive present day iron sulfide minerals greigite and mackinawite, yet we know little about how they form. In view of the likely role of such reactive minerals in the conversion of pre-biotic CO2 on Early Earth, we may well be able to harness iron sulfides as present-day catalysts for the same process, thereby potentially aiding the slowing down of climate change by converting the CO2 we produce into useful chemicals. In today's world, the importance of such iron-nickel-sulfide clusters as catalysts has been confirmed, as several life-essential iron-sulfur proteins help transform volatiles such as H2, CO and CO2 into other useful and less harmful chemicals. In all of the above examples, it is important to understand that the reactions that lead to the formation of all these minerals which are necessary for any of the geologically stable minerals to exist (i.e., pyrite) all rely on our understanding of the nucleation and growth of unstable precursors or of the reaction transforming one phase to another. Furthermore, the structure and reactivity of each of these phase determines its role and potential application in the environment. A few research groups in the UK and abroad have carried out high quality investigations of the properties of a number of iron sulfide minerals, but it is particularly difficult to investigate events early on in the nucleation process, even though they set the scene for all subsequent transformations. In this project we propose to employ a robust combination of state-of-the-art computation and experiment to unravel the nucleation of iron sulfide mineral phases. We aim to follow the reactions from the emergence of the first building block in solution, through agglomeration into larger clusters, their aggregation into nano-particles and the eventual transformation into the final crystal. We anticipate that this project, investigating short-lived processes which are only now accessible to study through the development of high temporal and spatial resolution in-situ characterization techniques and High Performance Computing platforms, will lead to in-depth step-by-step quantitative insight into the iron sulfide formation pathways and enhance our fundamental understanding of how a mineral nucleates in solution.
Data are either (1) depths and spacings between stylolites and faults within Unit IV, (2) images from IODP drill core image logs of the locations of samples observed, (3) photomicrographs and flatbed thin section scans of thin sections cut from samples, (4) SEM BSE or EDS data collected at Cardiff University. These data form the basis of: Leah et al. "Brittle-ductile strain localisation and weakening in pelagic sediments seaward of the Hikurangi margin, New Zealand", Tectonics, Submitted. Images and data from samples collected at IODP Expedition 375 Site U1520 (38°58.1532'S, 179°7.9112'E, 3522.1 mbsl). This is just seaward (east) of the trench of the Hikurangi Margin, New Zealand.