Role of coal type and rank on methane sorption characteristics of Bowen Basin, Australia coals

The effect of coal composition, particularly the organic fraction, upon gas sorption has been investigated for Bowen Basin and Sydney Basin, Australia coals. Maceral composition influences on gas retention and release were investigated using isorank pairs of hand-picked bright and dull coal in the rank range of high volatile bituminous (0.78% R_{o max}) to anthracite (3.01% R_{o max}). Adsorption isotherm results of dry coals indicated that Langmuir volume (V_L) for bright and dull coal types followed discrete, second-order polynomial trends with increasing rank. Bright coals had a minimum V_L at 1.72% R_{o max} and dull coals had a minimum V_L at 1.17% R_{o max}. At low rank, V_L was greater in bright coal by about 10 cm³/g, but as rank increased, the bright and dull trends converged and crossed at 1.65% R_{o max}. At ranks higher than 1.65% R_{o max}, both bright and dull coals followed similar trends. These competing trends mean that the importance of maceral composition on V_L varies according to rank. In high volatile bituminous coals, increases in vitrinite content are associated with increases in adsorption capacity. At ranks higher than medium to low volatile bituminous, changes in maceral composition may exert relatively little influence on adsorption capacity. The Langmuir pressure (P_L) showed a strong relationship of decreasing P_L with increasing rank, which was not related to coal type. It is suggested that the observed trend is related to a decrease in the heterogeneity of the pore surfaces, and subsequent increased coverage by the adsorbate, as coal rank increases. Desorption rate studies on crushed samples show that dull coals desorb more rapidly than bright coals and that desorption rate is also a function of rank. Coals of lower rank have higher effective diffusivities. Mineral matter was found to have no influence on desorption rate of these finely crushed samples. The evolution of the coal pore structure with changing rank is implicated in diffusion rate differences.     

The Skien lavas, Oslo Rift: petrological disequilibrium and geochemical evolution

The Skien lavas, which form the earliest phase of basaltic magmatism within the Permo-Carboniferous Oslo Rift, contain multiple generations of clinopyroxene which exhibit strong petrological and geochemical disequilibrium. Three principal core compositions have been identified: (1) low-jadeite, high-Mg, Cr-diopside cores (CrMgDi) with strongly depleted trace-element signatures, which are believed to be xenocrystic in origin; (2) Mg-rich, Cr-poor diopside cores (MgDi) with moderately depleted trace-element signatures which probably represent early cognate growth; and (3) more dominant, low-Mg, phenocrystic diopside cores (PhenDi). Several samples contain CrMgDi or MgDi cores which have been subjected to resorption and partial re-equilibration with their host melts, indicative of extensive disequilibrium and magma mixing. These three core types are overgrown by trace-element-enriched Ti-augite, which also forms megacrysts and late-stage lava groundmass. Calculated Ti-augite/melt partition coefficients show clinopyroxene compatibility of the M-HREE, Zr, Hf and Y. The LILE, Sr, and Nb remain incompatible. )Sr₃₀₀ and )Nd₃₀₀ of Ti-augite overgrowths, phenocrystic diopside, and MgDi diopside cores show that intrasample isotopic disequilibrium existed when the host basalts were erupted. All epsilon values lie within the range of data previously published for the Skien lavas. Detailed examination of the chemical, isotopic and textural disequilibrium features seen in these lavas has enabled us to place constraints upon the magmatic evolution of this basalt suite, ranging from xenocryst incorporation to cognate multistage pyroxene growth, as well as identifying clear evidence of magma mixing and possible crustal contamination.     

A model for O/O variations in CO2 evolved from goethite during the solid-state α-FeOOH to α-Fe2O3 phase transition

“Plateau” δ¹⁸O values of CO₂ that evolved from the Fe(CO₃)OH component during isothermal vacuum dehydrations (200-230 °C) of 18 natural goethites range from 8.2 to 28.1‰. In contrast, the measured δ¹⁸O values of the goethite structural oxygen range from −11.3 to 1.7‰. The results of this study indicate that the apparent oxygen isotope fractionation factor (¹⁸α_app) between plateau CO₂ and initial goethite is systematically related to the rate of isothermal vacuum dehydration. The nonlinear correlation and the magnitudes of the ¹⁸α_app values are predicted by a relatively simple mass balance model with the following assumptions: (1) the rate of isothermal vacuum dehydration of goethite (for the interval from 0 to ∼60 to 80% loss of structural hydroxyl hydrogen) can be reasonably well represented by first-order kinetics and (2) isotopic exchange between evolving H₂O vapor and solid occurs only in successive, local transition states. The generally good correspondence between the model predictions and the experimental data seems to validate these assumptions. Thus, the ¹⁸O/¹⁶O ratios of the evolved CO₂ can act as probes into the transient processes operating at the molecular level during the solid-state goethite-to-hematite phase transition. For example, the activation energy for the rate constant associated with the transition state, oxygen isotopic exchange between solid and H₂O vapor, is tentatively estimated as 28 ± 11 KJ/mol. Such knowledge may be of consequence in understanding the significance of ¹⁸O/¹⁶O ratios in hematites from some natural environments (e.g., Mars?).Kinetic data and δ¹⁸O values of CO₂ are routinely obtained in the course of measurements of the abundance and δ¹³C values of the Fe(CO₃)OH in goethite. The observed correlation between ¹⁸α_app and dehydration rates suggests that plateau δ¹⁸O values of evolved CO₂ may provide complementary estimates of the δ¹⁸O values of total goethite structural oxygen (O, OH, CO₂) with an overall precision of about ±1‰. However, because of isotopic exchange during the dehydration process, δ¹⁸O values of the evolved CO₂ do not reflect the original δ¹⁸O values of the CO₂ that was occluded as Fe(CO₃)OH in goethite.     

Geochemical and structural evolution of micas in the Rožná and Dobrá Voda pegmatites,Czech Republic

Summary The chemistry, structural parameters, polytypism, optical properties and Rb-Sr isotopes were examined in 11 to 60 samples of biotite, muscovite and lepidolite from the pegmatites at Roná (the type locality of lepidolite; 323 ± 4Ma) and Dobrá Voda (306 ± 9Ma) in western Moravia. At both localities, early endocontact biotite is followed inwards by muscovite and lepidolite, which is concentrated in and around the core. At Roná, a 1M lepidolite follows after 2M₁ muscovite but all later generations of lepidolite are 2M₂, close to Tri₅₀ Ply₅₀ and in part associated with muscovite 2M₁. At Dobrá Voda, all lepidolite types are 1M and free of muscovite, and the late varieties approximate Tri₃₀ Ply₇₀. At both localities, a trend of increasing HF is indicated during the progress of mica crystallization, culminating in precipitation of topaz. Polytypism of lepidolite is not correlatable with any compositional or growth feature, or their combination. Throughout the mica crystallization, Rb/Cs decreases but K/Rb becomes reversed after an initial decrease. Boron is partitioned preferentially into muscovite (up to 1.10 wt.% B₂O₃) but Be, Zn, Mn and Sc are enhanced in lepidolite. A slight increase in Fe, Ba and Cl in the last generation of lepidolite might be possibly due to mixing of residual pegmatite fluids with metamorphic pore solutions.

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Geochemische und strukturelle Entwicklung der Glimmer in den Pegmatiten von Roná und Dobrá Voda, Tschechische Republik

Zusammenfassung In 11 bis 60 Proben von Biotit, Muskovit und Lepidolith aus den Pegmatiten von Roná (Typlokalität des Lepidoliths; 323 ± 9 Ma) in Westmähren wurden Chemie, Struktur-parameter, Polytypie, optische Eigenschaften und Rb-Sr-Isotopie untersucht. An beiden Lokalitäten wird früher Biotit an Endokontakten nach Innen von Muskovit und Lepidolith gefolgt, letzterer ist in und um den Kern konzentriert. In Roná folgt 1M-Lepidolith auf 2M₁-Muskovit, aber alle späteren Lepidolithgenerationen sind 2M₂, nahe Tri₅₀Ply₅₀ und zum Teil mit 2M₁-Muskovit vergesellschaftet. In Dobrá Voda sind alle Lepidolithe vom Typ 1M und frei von Muskovit, die späten Varietäten kommen Tri₅₀Ply₅₀ nahe. An beiden Lokalitäten ist während des Fortschreitens der Glimmerkristallisation eine Tendenz von steigendem HF angezeigt, die in der Ausfällung von Topas ihren Höhepunkt findet. Die Polytypie des Lepidoliths kann nicht mit irgendeiner Eigenheit der Zusammensetzung oder des Wachstums korreliert worden, auch nicht mit einer Kombination von diesen. Während der ganzen Glimmerkristallisation nimmt Rb/Cs ab, aber die Tendenz von K/Rb ändert sich nach anfänglichem Abfall. Das Bor verteilt sich bevorzugt auf den Muskovit (bis zu 1.10 Gew. -% B₂O₃), aber die Be-, Zn-, Mn- und Sc-Gehalte sind im Lepidolith erhöht. Ein leichter Ansteig von Fe, Ba und Cl in der letzten Lepidolithgeneration könnte vielleicht durch eine Mischung von pegmatitischen Restlösungen mit metamorphen Porenlösungen verursacht sein.

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With 9 Figures     

Research and application in British geomorphology

Three aspects of the application of geomorphological research are identified: direct application of principles, methods and techniques; research and development specifically for application and the recognition of potentially applicable research. Some recent British work in each of these areas is reviewed.     

Aragonite in California Glaucophane Schists, and the Kinetics of the Aragonite--Calcite Transformation

Coleman & Lee's discovery that aragonite is a widespreadmetamorphic mineral in California glaucophane schists is confirmedand amplified. Methods of microscopic distinction between aragonite,calcite, and dolomite, including a universal-stage technique,are described. Further data are recorded regarding the paragenesisof aragonite-bearing glaucophane and lawsonite schists. Carbonatesin the greenschist facies are found to be exclusively calciteand dolomite. In many Californian metamorphic aragonites partialinversion to calcite has been observed. This appears to be anequal-volume replacement in which an a axis and an edge [f:f] of calcite—both directions of Closest spacing of Ca⁺⁺ions—commonlyare parallel to of the crystal axes a, b, and c of aragonite. The problem of survival of metamorphic aragonite through a necessarilylong period of post-metamorphic unloading is approached by experimentalexploration of the kinetics of the aragonite calcite transformation.It is found that Californian aragonite could survive unloadingfrom a depth of 20 km if the linear temperature gradient were10? C per km, but not appreciably higher. Available experimentaldata are consistent with crystallization of aragonite, jadeite,and lawsonite at depths of 20–30 km if a gradient of 10?C per km is assumed. The corresponding conditions of the glaucophane-schistfacies (T = 2OO?-3OO? C, P = 6000-9000 bars) are attributedessentially to deep burial in regions (subsiding geosyn-clines)of unusually low temperature gradient (10? C per km).     

Garnet crystal plasticity in the continental crust,new example from south Madagascar

Garnet (10 vol.%; pyrope contents 34–44 mol.%) hosted in quartzofeldspathic rocks within a large vertical shear zone of south Madagascar shows a strong grain‐size reduction (from a few cm to ～300 μm). Electron back‐scattered diffraction, transmission electron microscopy and scanning electron microscope imaging coupled with quantitative analysis of digitized images (PolyLX software) have been used in order to understand the deformation mechanisms associated with this grain‐size evolution. The garnet grain‐size reduction trend has been summarized in a typological evolution (from Type I to Type IV). Type I, the original porphyroblasts, form cm‐sized elongated grains that crystallized upon multiple nucleation and coalescence following biotite breakdown: biotite + sillimanite + quartz = garnet + alkali feldspar + rutile + melt. These large garnet grains contain quartz ribbons and sillimanite inclusions. Type I garnet is sheared along preferential planes (sillimanite layers, quartz ribbons and/or suitably oriented garnet crystallographic planes) producing highly elongated Type II garnet grains marked by a single crystallographic orientation. Further deformation leads to the development of a crystallographic misorientation, subgrains and new grains resulting in Type III garnet. Associated grain‐size reduction occurs via subgrain rotation recrystallization accompanied by fast diffusion‐assisted dislocation glide. This plastic deformation of garnet is associated with efficient recovery as shown by the very low dislocation densities (10¹⁰ m^?3 or lower). The rounded Type III garnet experiences rigid body rotation in fine‐grained matrix. In the highly deformed samples, the deformation mechanisms in garnet are grain‐size‐ and shape‐dependent: dislocation creep is dominant for the few large grains left (>1 mm; Type II garnet), rigid body rotation is typical for the smaller rounded grains (300 μm or less; Type III garnet) whereas diffusion creep may affect more elliptic garnet (Type IV garnet). The P–T conditions of garnet plasticity in the continental crust (≥950 °C; 11 kbar) have been identified using two‐feldspar thermometry and GASP conventional barometry. The garnet microstructural and deformation mechanisms evolution, coupled with grain‐size decrease in a fine‐grained steady‐state microstructure of quartz, alkali feldspar and plagioclase, suggests a separate mechanical evolution of garnet with respect to felsic minerals within the shear zone.     

GPR studies over the tsunami affected Karaikal beach,Tamil Nadu,south India

In this study, results of GPR profiling related to mapping of subsurface sedimentary layers at tsunami affected Karaikal beach are presented . A 400 MHz antenna was used for profiling along 262 m stretch of transect from beach to backshore areas with penetration of about 2.0 m depth (50 ns two-way travel time). The velocity analysis was carried out to estimate the depth information along the GPR profile. Based on the significant changes in the reflection amplitude, three different zones are marked and the upper zone is noticed with less moisture compared to other two (saturated) zones. The water table is noticed to vary from 0.5 to 0.75 m depth (12–15 ns) as moving away from the coastline. Buried erosional surface is observed at 1.5 m depth (40–42 ns), which represents the limit up to which the extreme event acted upon. In other words, it is the depth to which the tsunami sediments have been piled up to about 1.5 m thickness. Three field test pits were made along the transect and sedimentary sequences were recorded. The sand layers, especially, heavy mineral layers, recorded in the test pits indicate a positive correlation with the amplitude and velocity changes in the GPR profile. Such interpretation seems to be difficult in the middle zone due to its water saturation condition. But it is fairly clear in the lower zone located just below the erosional surface where the strata is comparatively more compact. The inferences from the GPR profile thus provide a lucid insight to the subsurface sediment sequences of the tsunami sediments in the Karaikal beach.     

Relationship between hydrocarbons and bacterial activity in mediterranean sediments: Part 2—hydrocarbon degrading activity of bacteria from sediments

In marine sediments from the Mediterranean coast polluted by oil spills (Etang de Berre) high bacterial activity is responsible for self-purification, samples collected from these areas showing a bacterial density several orders of magnitude higher than samples from non-polluted areas (Isle des Embiez). Between 60 and 80 % of the heterotrophic bacteria in the polluted areas are hydrocarbon-degrading, compared with 0.01 % in the non-polluted area.Several strains of hydrocarbon utilisers were isolated, a mixture of strains from each biotope was taken to represent a ‘biotope population’ and their activity towards different types of hydrocarbons (n-alkanes, iso-alkanes, cycloalkanes, aromatics) was determined.With ammonia as the nitrogen source the ‘biotope population’ from the polluted area degraded hydrocarbons much more readily than the ‘biotope population’ from the non-polluted area. With nitrate as the nitrogen source the degradation was much reduced, and, for some hydrocarbons, ceased in both ‘populations’.Individual hydrocarbons encouraged the growth of individual strains in the ‘biotope population’. In natural mixtures of hydrocarbons all strains grew well and degraded aliphatics. There was a good correlation between the respiratory activity of the ‘biotope population’ and the ability of the ‘population’ to utilise hydrocarbons for growth.