Down under or centre stage? The world images of Australian students

As part of a major international study, 219 first‐year geography students at three Australian universities drew sketch maps of the world. These maps were overwhelmingly Sinocentric in orientation. In terms of content, Australian students tended to include slightly fewer countries than students elsewhere. The level of inclusion of individual countries in the sketch maps was influenced greatly by the area and population of the countries in question but secondary factors such as proximity to Australia, Commonwealth nation status, historical/cultural factors and level of economic development were also important. In comparison to students throughout the world, Australian students demonstrated a fair knowledge of East Asia and ASEAN nations, Western Europe and Commonwealth nations, and relatively poor knowledge of Latin America, non‐Commonwealth Africa and South‐west Asia.     

Coelostat and heliostat: Theory of alignment

For perfectly aligned heliostats and coelostats tracking at the solar rate and half the solar rate, respectively, the solar beam has no translational motion. But, particularly in the field at eclipses, it is not possible to align heliostats and coelostats with infinite precision. We derive the effect of small misalignments on the translational motion of the beam, and give tables to allow the calculation of the accuracy to which the instruments must be mounted and adjusted to attain a desired accuracy over a given duration. Further, we show how to derive the necessary adjustments to improve alignment, given measurements of the tracking error.     

Hydrocode modeling of the Sierra Madera impact structure

Abstract— We present the first hydrocode simulations of the formation of the Sierra Madera structure (west Texas, USA), which was caused by an impact into a thick sedimentary target sequence. We modeled Sierra Madera using the iSALE hydrocode, and here we present two best‐fit models: 1) a crater with a rim (final crater) diameter of ?12 km, in agreement with previous authors' interpretations of the original structure, and 2) a crater ?16 km in diameter with increased postimpact erosion. Both models fit some of the geologic observational data, but discrepancies with estimates of peak shock pressure, extent of deformation, and stratigraphic displacement remain. This study suggests that Sierra Madera may be a larger crater than previously reported and illustrates some of the challenges in simulating impact deformation of sedimentary lithologies. As many terrestrial craters possess some amount of sedimentary rocks in the target sequence, numerical models of impacts into sedimentary targets are essential to our understanding of target rock deformation and the mechanics of crater formation.     

Chemical speciation and fate of tripolyphosphate after application to a calcareous soil

Adsorption and precipitation reactions often dictate the availability of phosphorus in soil environments. Tripolyphosphate (TPP) is considered a form of slow release P fertilizer in P limited soils, however, investigations of the chemical fate of TPP in soils are limited. It has been proposed that TPP rapidly hydrolyzes in the soil solution before adsorbing or precipitating with soil surfaces, but in model systems, TPP also adsorbs rapidly onto mineral surfaces. To study the adsorption behavior of TPP in calcareous soils, a short-term (48 h) TPP spike was performed under laboratory conditions. To determine the fate of TPP under field conditions, two different liquid TPP amendments were applied to a P limited subsurface field site via an in-ground injection system. Phosphorus speciation was assessed using X-ray absorption spectroscopy, total and labile extractable P, and X-ray diffraction. Adsorption of TPP to soil mineral surfaces was rapid (< 48 h) and persisted without fully hydrolyzing to ortho-P. Linear combination fitting of XAS data indicated that the distribution of adsorbed P was highest (~ 30–40%) throughout the site after the first TPP amendment application (high water volume and low TPP concentrations). In contrast, lower water volumes with more concentrated TPP resulted in lower relative fractions of adsorbed P (15–25%), but a significant increase in total P concentrations (~ 3000 mg P kg soil) and adsorbed P (60%) directly adjacent to the injection system. This demonstrates that TPP application increases the adsorbed P fraction of calcareous soils through rapid adsorption reactions with soil mineral surfaces.     

Analysis of experimental data on divalent cation diffusion kinetics in aluminosilicate garnets with application to timescales of peak Barrovian metamorphism,Scotland

We present a new statistical framework to analyze the diffusion data for divalent cations (Fe, Mg, Mn, and Ca) in aluminosilicate garnet using published experimental data and an Arrhenius relationship that accounts for dependence on temperature, pressure, garnet unit-cell dimension, and oxygen fugacity. The regression is based on Bayesian statistics and is implemented by the Markov chain Monte Carlo approach. All reported experimental uncertainties are incorporated, and the data are weighted by the precision of the experimental conditions. We also include a new term, the inter-experiment bias, to compensate for possible inconsistencies among experiments and to represent any experimental variability not explicitly presented in the Arrhenius relationship (e.g., water content, defect density). At high temperatures where most experiments were conducted, the diffusion coefficients calculated with the new parameters agree well with previous diffusion models (e.g., Chakraborty and Ganguly in Contrib Mineral Petrol, 111:74–86, 1992; Carlson in Am Mineral, 91:1–11, 2006). However, the down-temperature extrapolation leads to notable differences at lower temperatures for common petrological applications. For example, at 600 °C, the diffusion coefficients of Fe and Mn are one half-to-one order of magnitude faster and the diffusion coefficient of Ca is about one order of magnitude slower than calculated with parameters in Carlson (2006). Our statistical analysis also provides well-defined uncertainty bounds for timescale estimates based on garnet diffusion profiles. Application of the newly derived coefficients indicates that the timescale of the thermal peak of Barrovian metamorphism (Dalradian belt of Scotland) is about four to seven times longer than that estimated using previously published diffusion coefficients. The peak is still geologically brief, however—of the order of 10⁶ years (0.75 Myr +0.70/?0.36 Myr; ±1σ). This brevity requires pulsed advective heat input, as provided by syn-orogenic mafic magmatism in these rocks.     

Mineralogy,nucleation and growth of dolomite in the laboratory and sedimentary environment: A review

Dolomite [CaMg(CO₃)₂] forms in numerous geological settings, usually as a diagenetic replacement of limestone, and is an important component of petroleum reservoir rocks, rocks hosting base metal deposits and fresh water aquifers. Dolomite is a rhombohedral carbonate with a structure consisting of an ordered arrangement of alternating layers of Ca²⁺ and Mg²⁺ cations interspersed with anion layers normal to the c‐axis. Dolomite has symmetry, lower than the (CaCO₃) symmetry of calcite primarily due to Ca–Mg ordering. High‐magnesium calcite also has symmetry and differs from dolomite in that Ca²⁺ and Mg²⁺ ions are not ordered. High‐magnesium calcite with near‐dolomite stoichiometry (≈50 mol% MgCO₃) has been observed both in nature and in laboratory products and is referred to in the literature as protodolomite or very high‐magnesium calcite. Many dolomites display some degree of cation disorder (Ca²⁺ on Mg²⁺ sites and vice versa), which is detectable using transmission electron microscopy and X‐ray diffractometry. Laboratory syntheses at high temperature and pressure, as well as studies of natural dolomites show that factors affecting dolomite ordering, stoichiometry, nucleation and growth include temperature, alkalinity, pH, concentration of Mg and Ca, Mg to Ca ratio, fluid to rock ratio, mineralogy of the carbonate being replaced, and surface area available for nucleation. In spite of numerous attempts, dolomite has not been synthesized in the laboratory under near‐surface conditions. Examination of published X‐ray diffraction data demonstrates that assertions of dolomite synthesis in the laboratory under near‐ambient conditions by microbial mediation are unsubstantiated. These laboratory products show no evidence of cation ordering and appear to be very high‐magnesium calcite. Elevated‐temperature and elevated‐pressure experiments demonstrate that dolomite nucleation and growth always are preceded by very high‐magnesium calcite formation. It remains to be demonstrated whether microbial‐mediated growth of very high‐magnesium calcite in nature provides a precursor to dolomite nucleation and growth analogous to reaction paths in high‐temperature experiments.