OH defects in quartz in the system quartz–albite–water and granite–water between 5 and 25?kbar

The incorporation of OH defects in quartz from the systems quartz–water, quartz–albite–water and granite–water at pressures between 5 and 25?kbar and temperatures between 800 and 1,000?°C was investigated by IR spectroscopy. The two most important OH absorption features can be assigned to hydrogarnet defects (absorption band at 3,585?cm^?1) and coupled substitutions involving Al³⁺ (Al–H defects, absorption bands at 3,310, 3,378 and 3,430?cm^?1). Al incorporation in quartz is controlled by mineral/melt partitioning (D _Al ^Qz/Melt ?=?0.01) and exhibits a negative pressure dependence. This trend is not clearly reflected by the concentration of Al–H defects, which shows positive deviations from the theoretical 1:1 correlation of Al/H for some samples. In contrast to the Al–H defects, formation of hydrogarnet defects appears to be positively correlated to pressure and water activity, and may be used a petrological indicator. The overall water concentration exhibits only minor changes with pressure and temperature, but a clear correlation of water activity (controlled by various amounts of dissolved salts) and hydrogarnet substitution could be established.     

Electrical conductivity of H-bearing orthopyroxene single crystals measured with impedance spectroscopy

In this study, the electrical conductivity of synthetic and natural orthopyroxene single crystals containing various amounts of hydrogen and cation impurities (i.e., Al, Fe) was investigated using impedance spectroscopy. A new cell was developed to measure conductivities of submillimeter-sized oriented single crystals with impedances up to 10¹⁰?Ohm. In contrast to previous studies on olivine and orthopyroxene, results from this study do not show a simple correlation of the concentration of protons and the electrical conductivity. Instead, the electrical conductivity appears to be a complex function of iron content, hydrogen content, crystal orientation and concentration of other impurity cations and shows similar activation energies to hydrogen diffusion. Model calculations considering proton conduction rather exclude than suggest orthopyroxene as responsible phase for high-conductivity regions in the Earth’s upper mantle.     

Early Triassic potassic volcanism in the Afyon Zone of the Anatolides/Turkey: implications for the rifting of the Neo-Tethys

Afyon Zone, which was derived from the Anatolide–Tauride platform during closure of the Neo-Tethys, is made up of pre-Mesozoic basement and unconformably overlying Triassic–Early Tertiary cover series. The Afyon Zone contains widespread metavolcanic rocks, which are dominated by rhyolite, dacite, and trachyandesite. They form a distinct volcanic succession, which is separated from the underlying Silurian–Lower Carboniferous metacarbonates and meta-siliciclastics by a regional unconformity. Trachyandesitic metavolcanics are made up of massive lava flows, pyroclastics and epiclastics, less frequently, domes and dikes, which were developed on a deeply eroded subaerial landmass. U/Pb and Pb/Pb zircon geochronology yielded Lower Triassic (~250 Ma) ages, which are interpreted as extrusion age of trachyandesitic volcanics. Based on the stratigraphic, geochronological, and geochemical data, we suggest that these Lower Triassic magmatic rocks represent an extensional tectonic setting on the northern active margin of the Gondwana, which led to the development of the northern branch of the Neo-Tethys.     

The burial efficiency of organic carbon in the sediments of Lake Kinneret

Even though lake sediments constitute a significant long-term carbon sink, studies on the regulation of carbon burial in lakes sediments have, to date, been surprisingly few. We investigated to what degree the organic carbon (OC) being deposited onto the bottom of Lake Kinneret (Israel) is buried in the sediment at four different sites with varying degrees of oxygenation and varying supply of allochthonous particles from the River Jordan. For estimation of the OC burial efficiency (OC BE), i.e., the ratio between buried and deposited OC, we calculated OC burial from dated sediment cores, and calculated OC deposition using three different approaches. Calculation of OC deposition from sediment trap-derived mass deposition rates multiplied with the OC content of surface sediment yielded OC BE values that were at odds with published values for sediments dominated by autochthonous OC sources. Calculation via sediment trap data on organic matter flux collected within the Lake Kinneret monitoring program, as well as calculation of OC deposition as the sum of OC burial plus OC mineralization, returned fairly congruent estimates of OC BE (range 10–41%), but only if the sediment trap data were corrected for the proportion of resuspended particles in the traps. Differences in OC BE between sites were small, indicating that OC source (common to all sites) was a more important regulator of OC BE in Lake Kinneret than oxygen exposure or mineral particles characteristics.     

Evidence for Century-Timescale Acceleration in Mean Sea Levels and for Recent Changes in Extreme Sea Levels

Two of the most important topics in Sea Level Science are addressed in this paper. One is concerned with the evidence for the apparent acceleration in the rate of global sea level change between the nineteenth and twentieth centuries and, thereby, with the question of whether the twentieth century sea level rise was a consequence of an accelerated climate change of anthropogenic origin. An acceleration is indeed observed in both tide gauge and saltmarsh data at different locations around the world, yielding quadratic coefficients ??c?? of order 0.005 mm/year², and with the most rapid changes of rate of sea level rise occurring around the end of the nineteenth century. The second topic refers to whether there is evidence that extreme sea levels have increased in recent decades at rates significantly different from those in mean levels. Recent results, which suggest that at most locations rates of change of extreme and mean sea levels are comparable, are presented. In addition, a short review is given of recent work on extreme sea levels by other authors. This body of work, which is focused primarily on Europe and the Mediterranean, also tends to support mean and extreme sea levels changing at similar rates at most locations.     

The potential use of OH-defects in enstatite as geobarometer

In this study, single crystals of pure enstatite (Mg₂Si₂O₆) were synthesised under water-saturated conditions at 4 and 8 GPa and 1,150°C with variable silica activity, leading to phase assemblages enstatite + forsterite, enstatite or enstatite + coesite. Run products were investigated using an FTIR spectrometer equipped with a focal plane array detector enabling IR imaging with a lateral pixel resolution of 2.7 μm. IR spectra within the OH-absorption region show two different groups of absorption bands: group 1 (wavenumbers at 3,592 and 3,687 cm^?1) shows strongest absorptions for E||n _β, whereas group 2 (wavenumbers at 3,067 and 3,362 cm^?1) shows strongest absorptions for E||n _γ. The groups are related to different defect types, group 1 to tetrahedral defects (T-site vacancies) and group 2 to octahedral defects (M-site vacancies). The intensity ratio of the bands within one group (i.e. A ₃₀₆₇/A ₃₃₆₂ and A ₃₅₉₂/A ₃₆₈₇) and the intensity ratio of E||n _γ and E||n _α in group 2 bands remain constant within error. In contrast, the intensity ratio of group 2 to group 1 absorption bands [e.g. (A ₃₃₆₂)/(A ₃₆₈₇)] is sensitive to the SiO₂ activity and pressure. On the basis of the results of this and previous studies, a barometer for pure orthoenstatite coexisting with forsterite can be formulated:\( P\,[{\text{GPa}}] = 1.056 + \sqrt {{\frac{{1.025 - A_{{\left( {3362} \right)/\left[ {(3362) + (3687)} \right]}} }}{0.009}}} , \) where A ₍₃₃₆₂₎ and A ₍₃₆₈₇₎ are the integral absorbances of the component E||n _γ of the absorption bands at 3,362 cm^?1 and the component E||n _β of the absorption band at 3,687 cm^?1, respectively.     

A lacustrine GDGT-temperature calibration from the Scandinavian Arctic to Antarctic: Renewed potential for the application of GDGT-paleothermometry in lakes

Quantitative climate reconstructions are fundamental to understand long-term trends in natural climate variability and to test climate models used to predict future climate change. Recent advances in molecular geochemistry have led to calibrations using glycerol dialkyl glycerol tetraethers (GDGTs), a group of temperature-sensitive membrane lipids found in Archaea and bacteria. GDGTs have been used to construct temperature indices for oceans (TEX₈₆ index) and soils (MBT/CBT index). The aim of this study is to examine GDGT-temperature relationships and assess the potential of constructing a GDGT-based palaeo-thermometer for lakes. We examine GDGT-temperature relationships using core top sediments from 90 lakes across a north-south transect from the Scandinavian Arctic to Antarctica including sites from Finland, Sweden, Siberia, the UK, Austria, Turkey, Ethiopia, Uganda, Chile, South Georgia and the Antarctic Peninsula. We examine a suite of 15 GDGTs, including compounds used in the TEX₈₆ and MBT/CBT indices and reflecting the broad range of GDGT inputs to small lake systems.GDGTs are present in varying proportions in all lakes examined. The TEX₈₆ index is not applicable to our sites because of the large relative proportions of soil derived and methanogenic components. Similarly, the MBT/CBT index is also not applicable and predicts temperatures considerably lower than those measured. We examine relationships between individual GDGT compounds and temperature, pH, conductivity and water depth. Temperature accounts for a large and statistically independent fraction of variation in branched GDGT composition. We propose a GDGT-temperature regression model with high accuracy and precision (R² = 0.88; RMSE = 2.0 °C; RMSEP = 2.1 °C) for use in lakes based on a subset of branched GDGT compounds and highlight the potential of this new method for reconstructing past temperatures using lake sediments.     

Analytical model for screening potential CO<Subscript>2</Subscript> repositories

Assessing potential repositories for geologic sequestration of carbon dioxide using numerical models can be complicated, costly, and time-consuming, especially when faced with the challenge of selecting a repository from a multitude of potential repositories. This paper presents a set of simple analytical equations (model), based on the work of previous researchers, that could be used to evaluate the suitability of candidate repositories for subsurface sequestration of carbon dioxide. We considered the injection of carbon dioxide at a constant rate into a confined saline aquifer via a fully perforated vertical injection well. The validity of the analytical model was assessed via comparison with the TOUGH2 numerical model. The metrics used in comparing the two models include (1) spatial variations in formation pressure and (2) vertically integrated brine saturation profile. The analytical model and TOUGH2 show excellent agreement in their results when similar input conditions and assumptions are applied in both. The analytical model neglects capillary pressure and the pressure dependence of fluid properties. However, simulations in TOUGH2 indicate that little error is introduced by these simplifications. Sensitivity studies indicate that the agreement between the analytical model and TOUGH2 depends strongly on (1) the residual brine saturation, (2) the difference in density between carbon dioxide and resident brine (buoyancy), and (3) the relationship between relative permeability and brine saturation. The results achieved suggest that the analytical model is valid when the relationship between relative permeability and brine saturation is linear or quasi-linear and when the irreducible saturation of brine is zero or very small.