Modelling rainfall/watertable relations using linear response functions

Linear system theory can be used to model and predict watertable responses to precipitation inputs in an artificially drained field. The response function is mathematically equivalent to the Unit Hydrograph concept familiar to hydrologists. This paper shows that it is possible to derive such response functions, and comments on the problems encountered in their derivation. Response functions for two contrasted sites are presented, and the possibilities for their use discussed.     

Occurrence and possible significance of rare Ti oxides (Magnéli phases) in carbonaceous chondrite matrices

Abstract— Rare, ultrafine-grained Ti oxides (Ti₃O₅ and the Magnéli phases, Ti₅O₉ and Ti₈O₁₅) have been identified by transmission electron microscopy in the CM2 carbonaceous chondrite, Bells and a carbonaceous chondrite matrix clast from the Nilpena polymict ureilite. In both meteorites the Ti oxides occur in the matrix as isolated grains and clusters of two or more grains. They are euhedral in shape and have grain sizes of 0.05–0.3 μm. Magnéli phases have been recently shown to be a common component in some interplanetary dust particles, but this is the first reported occurrence in a meteorite. The morphological properties and grain size of the Ti oxides are consistent with formation by vapor phase condensation either within the solar nebula or possibly in a presolar environment.     

Spatial geochemistry of a Carboniferous platform-margin-to-basin transect: Balancing environmental and diagenetic factors

Conventional (one-dimensional) chemostratigraphy of marine carbonates assesses the chemical archive of individual stratigraphic sections and their correlation in space and time. Whereas this approach has shown to be of value when linking isobathymetric domains, usually characterised by similar facies, more caution is needed when correlations are extended across different physiographic settings and hence different facies belts. Here, the spatial geochemical record of Pennsylvanian platform-margin-to-basin transects across a bathymetric range of about 800 m is documented and discussed in a process-oriented context. Particularly, the presence of layered palaeo-water masses and their potential control on slope facies distribution and geochemical properties requires attention. Whereas Carboniferous thermo- and/or chemo-clines most likely affected depth-related slope facies zonation, it was facies change and hence, variances in porosity–permeability properties, that controlled differential early burial diagenetic alteration. Specifically, the lower-slope related breccia facies is characterised by higher volumes of early burial carbonate cements. This implies that these sediments entered the shallow-burial domain with a considerable open pore space and gave way to an increased rock:fluid ratio. Whereas the δ¹³C record is invariant with bathymetry, the more diagenesis-sensitive δ¹⁸O proxy, records pronounced shifts observed across major facies boundaries. From this it is concluded that although the primary controlling factor of slope facies distribution with depth is probably palaeoceanographic in nature, it is differential rock:fluid ratios that control the first-order, spatial shifts in δ¹⁸O composition. These findings show that one-dimensional chemostratigraphy will severely underestimate the complexity of three-dimensional (bathymetric) data sets across platform margins. This is of relevance for the interpretation of the geochemical archive of fossil carbonate platforms in general.     

Evaluating the influence of mixture composition on the kinetics of salt damage in wall paintings using time lapse video imaging with direct data annotation

This paper presents an examination of the timescale of phase transition behaviour of a series of salts known to cause damage to wall paintings and other cultural property. The rate of deliquescence and crystallisation of single salts (nitromagnesite and halite) under different RH regimes, and the extent to which this was affected when mixed with other salts (niter, nitratite and gypsum), was investigated. The study was conducted using simple conventional techniques (mass measurements over time) and also using an innovative new method: timelapse video imaging with online data annotation. The results demonstrate the synergy gained from combining video imaging with environmental data in reference to time in the study of salt phase changes: where it revealed new information concerning the kinetics of deliquescence and crystallisation. The implications of these results for the implementation of environmental control measures within historic buildings are discussed.

High-pressure experimental growth of diamond using C–K2CO3–KCl as an analogue for Cl-bearing carbonate fluid

High-pressure, high-temperature diamond growth experiments have been conducted in the system C–K₂CO₃–KCl at 1050–1420 °C, 7.0–7.7 GPa. KCl is of interest because of the strong effect of halogens on the phase relations of carbonate-rich systems [Geophys. Res. Lett. 30 (2003) 1022] and because of the occurrence of KCl coexisting with alkali silicate–carbonate fluids in natural-coated diamond [Geochim. Cosmochim. Acta 64 (2000) 717]. We have used system C–K₂CO₃–KCl as an analogue for these mantle fluids in diamond growth experiments. The presence of KCl reduces the potassium carbonate liquidus to ≤1000 °C at 7.7 GPa, allowing it to act as a solvent catalyst for diamond growth at temperatures below the continental geotherm. This is a reduction on the minimum diamond growth temperature reported in the alkali-carbonate–C–O–H system [Lithos 60 (2002) 145]. Diamond growth using carbonate solvent catalysts is characterised by a relatively long induction period. However, the addition of KCl also reduced the period for diamond growth in carbonate to 5 min; no such induction period appears to be necessary. It is suggested that KCl destabilises carbonate, allowing greater solubility and diffusion of carbon.     

Petrochronology of oxidized granulites from southern Peru

Sapphirine–quartz granulites from the Cocachacra region of the Arequipa Massif in southern Peru record early Neoproterozoic ultrahigh‐temperature metamorphism. Phase equilibrium modelling and zircon petrochronology are used to quantify timing and pressure–temperature (P–T) conditions of metamorphism. Modelling of three magnetite‐bearing sapphirine–quartz samples indicates peak temperatures of >950°C at ~0.7 GPa and a clockwise P–T evolution. Elevated concentrations of Al in orthopyroxene are also consistent with ultrahigh‐temperature conditions. Neoblastic zircon records ages of c. 1.0–0.9 Ga that are interpreted to record protracted ultrahigh‐temperature metamorphism. Th/U ratios of zircon of up to 100 reflect U‐depleted whole‐rock compositions. Concentrations of heavy rare earth elements in zircon do not show systematic trends with U–Pb age but do correlate with variable whole‐rock compositions. Very large positive Ce anomalies in zircon from two samples probably relate to strongly oxidizing conditions during neoblastic zircon crystallization. Low concentrations of Ti‐in‐zircon (<10 ppm) are interpreted to result from reduced titania activities due to the strongly oxidized nature of the granulites and the sequestration of titanium‐rich minerals away from the reaction volume. Whole‐rock compositions and oxidation state have a strong influence on the trace element composition of metamorphic zircon, which has implications for interpreting the geological significance of ages retrieved from zircon in oxidized metamorphic rocks.     

Rock Magnetic Investigation of Historical Lavas Used in Palaeointensity Studies

Five samples from historical lava flows on Mt. Etna, which had previously been used in a palaeointensity study, were examined using a combination of rock magnetic and microscopic techniques to elucidate the causes of failure of palaeointensity determination. The samples were characterised using a combination of low-temperature susceptibility (LT-), Bitter pattern imaging and scanning electron microscope (SEM). High-temperature susceptibility curves and hysteresis loops had been previously measured by Calvo et al. (2001). Of the five samples only one gave an accurate palaeointensity. This sample was deuterically oxidised and consisted of large exsolved ore grains. It was only possible to distinguish this sample either optically or magnetically from a similar sample by the LT- warming curves; the unsuccessful sample displayed alteration in the LT- warming curves, which was not readily observed in the high temperature susceptibility curves. It is proposed that the measurement of LT- curves before and after heating could be a more sensitive method of determining suitability for palaeointensity determination than previous rock magnetic pre-selection techniques.