Pseudo-infinite guide stars for multi-conjugated adaptive optics on extremely large telescopes

We introduce a novel concept to sense the wavefront for adaptive optics purposes in astronomy using a conventional laser beacon. The concept we describe involves treating the light scattered in the mesospheric sodium layer as if it comes from multiple rings located at infinity. Such a concept resembles an inverse Bessel beam and is particularly suitable for multi-conjugated adaptive optics on extremely large telescopes. In fact, as the sensing process uses light apparently coming from infinity, some problems linked to the finite distance and vertical extent of the guide source are solved. Since such a technique is able to sense a wavefront solely in the radial direction, we propose furthermore a novel wavefront sensor by combining the inverse Bessel beam approach with the recently introduced z -invariant technique for a pseudo-infinite guide star sensor.     

The transient response mechanism and Pi2 pulsations at substorm onset—Review and outlook

Pi2 pulsations are nowadays thought to be transient hydromagnetic signals associated with the build-up of a new stationary magnetosphere-ionosphere coupling system after the sudden formation of the substorm current wedge. To illustrate this transient response mechanism, we will first briefly describe the substorm current circuit. Subsequently, we will demonstrate that the gross characteristics of high-latitude Pi2 can be explained by the sudden switch-on of this current wedge during substorm onset if its westward expansion is taken into account. We will conclude by discussing some additional phenomena and processes (like conductivity and electron density gradients, kinetic Alfvén waves, ionospheric polarization electric fields, and mode coupling) which have to be included into a realistic model for Pi2 pulsations and thus timedependent magnetosphere-ionosphere coupling.     

Calcite dissolution kinetics in the system CaCO3-H2O-CO2 at high undersaturation

Dissolution rates of limestone covered by a water film open to a CO₂-containing atmosphere are controlled by the chemical composition of the CaCO₃-H₂O-CO₂ solution at the water-mineral interface. This composition is determined by the Ca²⁺-concentration at this boundary, conversion of CO₂ into H⁺ and in the solution, and by diffusional mass transport of the dissolved species from and towards the water-limestone interface. A system of coupled diffusion-reaction equations for Ca²⁺, , and CO₂ is derived. The Ca²⁺ flux rates at the surface of the mineral are defined by the PWP-empirical rate law. These flux rates by the rules of stoichiometry must be equal to the flux rates of CO₂ across the air-water interface. In the solution, CO₂ is converted into H⁺ and . At low water-film thickness this reaction becomes rate limiting. The time dependent diffusion-reaction equations are solved for free drift dissolution by a finite-difference scheme, to obtain the dissolution rate of calcite as a function of the average calcium concentration in the water film. Dissolution rates are obtained for high undersaturation. The results reveal two regimes of linear dissolution kinetics, which can be described by a rate law F = α_i(m_ic_eq − c), where c is the calcium concentration in the water film, c_eq the equilibrium concentration with respect to calcite. For index i = 0, a fast rate law, which here is reported for the first time, is found with α₀ = 3 × 10⁻⁶ m s⁻¹ and m₀ = 0.3. For c > m₀c_eq, a slow rate law is valid with α₁ = 3 × 10⁻⁷ m  s⁻¹ and m₁ = 1, which confirms earlier work. The numbers given above are valid for film thickness of several tenths of a millimetre and at 20 °C. These rates are proven experimentally, using a flat inclined limestone plate covered by a laminar flowing water film injected at an input point with known flow rate Q and calcium concentration. From the concentration measured after flow distance x the dissolution rates are determined. These experiments have been performed at a carbon-dioxide pressure of 0.00035 atm and also of 0.01 atm. The results are in good agreement to the theoretical predictions.     

Suppression of wind turbine noise from seismological data using nonlinear thresholding and denoising autoencoder

Journal of Seismology - Seismologists found a significant deterioration in station quality after installation of wind turbines (WTs), which led to conflicts between WT operators and seismic...     

Constraints on the source of Cu in a submarine magmatic-hydrothermal system,Brothers volcano,Kermadec island arc

Most magmatic-hydrothermal Cu deposits are genetically linked to arc magmas. However, most continental or oceanic arc magmas are barren, and hence new methods have to be developed to distinguish between barren and mineralised arc systems. Source composition, melting conditions, the timing of S saturation and an initial chalcophile element-enrichment represent important parameters that control the potential of a subduction setting to host an economically valuable deposit. Brothers volcano in the Kermadec island arc is one of the best-studied examples of arc-related submarine magmatic-hydrothermal activity. This study, for the first time, compares the chemical and mineralogical composition of the Brothers seafloor massive sulphides and the associated dacitic to rhyolitic lavas that host the hydrothermal system. Incompatible trace element ratios, such as La/Sm and Ce/Pb, indicate that the basaltic melts from L’Esperance volcano may represent a parental analogue to the more evolved Brothers lavas. Copper-rich magmatic sulphides (Cu?>?2 wt%) identified in fresh volcanic glass and phenocryst phases, such as clinopyroxene, plagioclase and Fe–Ti oxide suggest that the surrounding lavas that host the Brothers hydrothermal system represent a potential Cu source for the sulphide ores at the seafloor. Thermodynamic calculations reveal that the Brothers melts reached volatile saturation during their evolution. Melt inclusion data and the occurrence of sulphides along vesicle margins indicate that an exsolving volatile phase extracted Cu from the silicate melt and probably contributed it to the overlying hydrothermal system. Hence, the formation of the Cu-rich seafloor massive sulphides (up to 35.6 wt%) is probably due to the contribution of Cu from a bimodal source including wall rock leaching and magmatic degassing, in a mineralisation style that is hybrid between Cyprus-type volcanic-hosted massive sulphide and subaerial epithermal–porphyry deposits.     

The Impact Of Extreme Summer Melt on Net Accumulation of an Avalanche Fed Glacier,as Determined by Ground‐Penetrating Radar

Glacier mass balance is more sensitive to warming than cooling, but feedbacks related to the exposure of previously buried firn and ice in very warm years is not generally considered in sensitivity studies. A ground‐penetrating radar survey in the accumulation area of Rolleston Glacier, New Zealand shows that five years of previous net accumulation was removed by melt from parts of the glacier above the long‐term equilibrium line altitude during a single negative mass balance year. Rolleston Glacier receives a large amount of accumulation from snow avalanches, which may temporarily buffer it from climate warming by providing additional mass that has accumulated at higher elevations, effectively increasing the elevation range of the glacier. However, glaciers reliant on avalanche input may have high sensitivity to climatic variations because the extra mass is concentrated on a small part of the glacier, and small variations in avalanche input could have a large impact on overall glacier accumulation. Further research is needed to better estimate the amount and spatial distribution of accumulation by avalanche in order to quantify the climate sensitivity of small avalanche‐fed glaciers.     

Flow network derivation from a high resolution DEM in a low relief,agrarian landscape

Digital flow networks derived from digital elevation models (DEMs) sensitively react to errors due to measurement, data processing and data representation. Since high‐resolution DEMs are increasingly used in geomorphological and hydrological research, automated and semi‐automated procedures to reduce the impact of such errors on flow networks are required. One such technique is stream‐carving, a hydrological conditioning technique to ensure drainage connectivity in DEMs towards the DEM edges. Here we test and modify a state‐of‐the‐art carving algorithm for flow network derivation in a low‐relief, agricultural landscape characterized by a large number of spurious, topographic depressions. Our results show that the investigated algorithm reconstructs a benchmark network insufficiently in terms of carving energy, distance and a topological network measure. The modification to the algorithm that performed best, combines the least‐cost auxiliary topography (LCAT) carving with a constrained breaching algorithm that explicitly takes automatically identified channel locations into account. We applied our methods to a low relief landscape, but the results can be transferred to flow network derivation of DEMs in moderate to mountainous relief in situations where the valley bottom is broad and flat and precise derivations of the flow networks are needed. Copyright © 2013 John Wiley & Sons, Ltd.     

Exploring aberrant bivalve shell ultrastructure and geochemistry as proxies for past sea water acidification

Throughout much of Earth's history, marine carbonates have represented one of the most important geological archives of environmental change. Several pivotal events during the Phanerozoic, such as mass extinctions or hyperthermal events have recently been associated with ocean acidification. Nevertheless, well‐defined geological proxies for past ocean acidification events are, at best, scarce. Here, experimental work explores the response of bivalve shell ultrastructure and isotope geochemistry (δ¹³C, δ¹⁸O and δ²⁶Mg) to stressful environments, in particular to sea water acidification. In this study, the common blue mussel, Mytilus edulis, was cultured (from early juvenile stages to one year of age) at four pH regimes (pH_NBS 7·2 to pH 8·0). Shell growth rate and ultrastructure of mainly the calcitic portion of the shells were compared between experimental treatments. Specimens exposed to low‐pH environments show patches of disordered calcitic fibre orientation in otherwise well‐structured shells. Furthermore, the electron backscattered diffraction analyses reveal that, under acidified conditions, the c‐axis of the calcite prisms exhibits a bimodal or multi‐modal distribution pattern. Similar shell disorder patterns have been reported from mytilids kept under naturally acidified sea water conditions. In contrast, this study found no evidence that different pH regimes affect shell carbon, oxygen or magnesium isotope ratios. Based on these observations, it is proposed that: (i) stressful environments, in this case low sea water pH, predictably affect bivalve biomineralization patterns; and (ii) these findings bear potential as a novel (petrographic) proxy for ancient sea water acidification. An assessment of the applicability of these data to well‐preserved fossil shell material from selected time intervals requires additional work.     

Simplified synthesis of an 8-hydroxyquinoline chelating resin and a study of trace metal profiles from Jellyfish Lake, Palau

We report a simplified synthesis, and some performance characteristics, for 8-hydroxyquinoline (8-HOQ) covalently bonded to a chemically resistant TosoHaas TSK vinyl polymer resin. The resin was used to concentrate trace metals from stored, acidified seawater samples collected from Jellyfish Lake, an anoxic marine lake in the Palau Islands. The Mn, Fe, and Zn profiles determined from the 8-HOQ resin extraction were similar to those determined using Chelex-100 resin. The Zn and Cd profiles did not exhibit removal by sulfide “stripping” in contrast to other anoxic marine basins. The profiles of Co and Ni also exhibited elevated concentrations in the anoxic hypolimnion. The solution speciation and saturation states for the metals were calculated using revised metal-bisulfide stability constants. The calculations suggest that the MS(HS)⁻ species dominates the solution speciation for Mn, Co, Ni, Zn, Cd, and Pb. Cu(I) is modeled as the CuS⁻ or Cu(HS)₂⁻ species, while Fe(II) behaves as the free Fe²⁺ cation. The Mn, Co, Ni, Cu and Cd concentrations appeared to be at least 10-fold undersaturated, while the Fe(II), Zn, and Pb concentrations were close to saturation with respect to their metal sulfides.