Mechanisms of orthopyroxene dissolution in silica-undersaturated melts at 1 atmosphere and implications for the origin of silica-rich glass in mantle xenoliths

Experiments dissolving orthopyroxene (En₉₃) in a variety of Si-undersaturated alkaline melts at 1 atmosphere and variable f _O2 demonstrate that orthopyroxene dissolves to form olivine, Si-rich melt and clinopyroxene. These phases form a texturally and chemically distinct boundary layer around the partly dissolved orthopyroxene crystals. The occurrence of clinopyroxene in the boundary layer is due to inward diffusion of Ca from the solvent melt to the boundary layer causing clinopyroxene saturation. Compositional profiles through the solvent and the boundary layer for a number of experiments demonstrate rapid diffusion of cations across the boundary layer – solvent interface. SiO₂ diffuses outward from the boundary layer whereas CaO and Al₂O₃ diffuse toward the Si-enriched boundary layer melt. The rate of Al diffusion is slower under reducing conditions compared to the rates in experiments performed in air. Concentrations of FeO and MgO in the boundary layer and solvent are approximately equal indicating rapid diffusion and attainment of equilibrium despite ongoing crystallisation of clinopyroxene within the boundary layer. The behaviour of Na₂O and K₂O is strongly affected by f _O2. Under reducing conditions Na₂O and K₂O concentrations are approximately equal in the boundary layer and solvent indicating normal diffusion down the concentration gradient and attainment of equilibrium. Under oxidising conditions, K₂O and to a lesser extent Na₂O, have compositional profiles indicative of uphill diffusion likely due to their preference for more polymerised Si- and Al-rich melts. Under reduced conditions Al-enrichment in the boundary layer melt is not as extreme and uphill diffusion did not occur. The composition of the solvent melt after the experiments indicates that it was contaminated by the boundary layer by convective mixing due to the onset of hydrodynamic instabilities brought on by density and viscosity contrasts between the two melts. Despite using a wide variety of solvent melt compositions we find that the boundary layer melts converge toward a common composition at high SiO₂ contents. The composition of glass generated by orthopyroxene dissolution at 1 atmosphere is similar in many respects to Si-rich glass found in many orthopyroxene-rich mantle xenoliths that have been attributed to high pressure in situ processes including mantle metasomatism. The results of this study suggest that at least some Si-rich melts are likely to have formed by dissolution of xenolith orthopyroxene at low pressure possibly by their Si-undersaturated host magmas. Received: 30 August 1996 / Accepted: 15 April 1998     

Isotopic and geochemical evidence for magma mixing in the petrogenesis of the Coire Uaigneich Granophyre,Isle of Skye,N.W. Scotland

Field relations, petrographic features, major and selected trace element compositions, and Sr- and Pb- isotope characteristics indicate that the Coire Uaigneich Granophyre (CUG) was formed by the mixing of two magmas. One of these, a liquid of high ⁸⁷Sr/⁸⁶Sr ratio (ca. 0.731) formed by the anatexis of late Precambrian Torridonian sediments, contained relict quartz and zircon. The other liquid was an acid differentiate of basaltic magma and was enriched in incompatible elements such as Zr and Y. The two magmas mixed in the proportions of approximately two parts anatectic melt to one part acid differentiate. Hydrothermal metamorphism had no significant effect on the bulk chemistry of the CUG.     

A review of wave-dominated clastic shoreline deposits

Barrier islands, beaches, wave-dominated deltas and chenier plains probably form more than one-fifth of present coasts, and constitute an even larger proportion of the subsiding lowland coasts likely to be preserved in the stratigraphic record. The geometry, vertical sequences and composition of their deposits are the result of: (1) shoreline behaviour, whether transgressive, regressive or stable; (2) physical processes, particularly the relative intensities of waves and tides; (3) climate; (4) global tectonic setting; and (5) topography of underlying deposits.Published interpretations indicate that equivalent deposits are abundant in the geological record. Sandstones are mostly quartzose, cemented by carbonates and quartz, and have sheet or linear geometries. Ancient deposits can provide evidence of palaeogeography and some are economically significant, particularly as hydrocarbon reservoir rocks.Four end-member sedimentation models are proposed for the interpretation of ancient deposits: (1) transgressive sheet sands associated with deltas; (2) non-deltaic transgressive sheet sands; (3) regressive sheet sands; and (4) linear sand bodies. Probable depositional settings, geometries, characteristics of deposits and palaeocurrent patterns are discussed.     

Model systems for anatexis of pelitic rocks

Subsolidus and melting reactions involving calcic plagioclase in pelitic assemblages in the K-Na-Ca model system occur at higher temperatures than their K-Na counterparts. For the most calcic plagioclase compositions observed in high-grade pelitic rocks (An₂₅-An₄₀) the equilibria are rarely extended by more than 30 ° C above those in KA1O₂-NaAlO₂-Al₂O₃-SiO₂-H₂O, although all discontinuities in facies inferred for the K-Na system are continuously displaced when they involve Ca-bearing plagioclase. The maximum pressure-temperature overlap between muscovite dehydration and initial melting reactions occurs in the pressure range of 4–6 kbar between about 640 ° and 720 ° C. This provides optimum conditions for anatectic melt generation in felsic rocks of the appropriate compositions progressively metamorphosed in kyanite-sillimanite facies series. Progressive regional metamorphism at pressures of 2–4 kbar, corresponding to andalusite-sillimanite facies series, shows little overlap between muscovite dehydration and initial melting reactions. Consequently anatectic melt generation in andalusite-sillimanite facies series would require the participation of biotite in dehydration-melting reactions. Felsic intrusive rock in andalusite-sillimanite terranes could have risen upward from their anatectic sites in high grade kyanite-sillimanite facies series at depth. Many andalusite-sillimanite facies series terranes culminating in migmatites could represent upward movement of kyanite-sillimanite facies series rocks to shallower depths with uplift rates faster than cooling rates.     

The age,origin, and volcanological significance of the Y-5 ash layer in the Mediterranean

The Y-5 ash is the most widespread layer in deep-sea sediments from the eastern Mediterranean. This ash layer was previously correlated with the Citara-Serrara tuff on Ischia Island and dated at approximately 25,000 yr B.P. New data on the glass chemistry of the Y-5 ash and pyroclastic deposits from the Neopolitan volcanic province suggest that the layer is correlative with the large-volume Campanian ignimbrite and not with the deposit from Ischia Island. The volume of the Y-5 ash is approximately 65 km³ which is comparable in magnitude to the volume of the Campanian ignimbrite. An interpolated age of approximately 38,000 yr B.P. is estimated based on sedimentation rates derived from δ¹⁸O stratigraphy. There is a discrepancy between this estimate and previously reported radiocarbon ages which range from 24,000 to 35,000 yr B.P. We propose that the “Campanian tuff ash layer” should be adopted as the full stratigraphic name for the Y-5 ash. The deep-sea ash layer is divisible into two units in proximal localities, probably correlating with two major phases of the eruption: plinian and ignimbrite.     

Garnet growth in a metapelite from the Moinian rocks of Northern Sutherland,Scotland

Compositional profiles of a series of garnets, extracted from a pelitic schist occurring in the Moinian rocks of Northern Sutherland, have been established. The profiles are complex and do not conform to a simple fractionation model. A model to explain them is suggested.     

Diagenesis of Cretaceous sandstones of the Kootenay Formation at Elk Valley (southeastern British Columbia) and Mt Allan (southwestern Alberta)

Vitrinite reflectance data for two sections of the Kootenay Formation are different, but increase with depth. Illite crystallinities (XRD) are irregular with depth but detailed S.E.M. examination shows that crystal size and morphology increase with depth.At Elk Valley (low reflectance) S.E.M. examination shows kaolinite + dolomite as the authigenic assemblage. At Mt Allan (45 km north, higher reflectance) kaolinite disappears at 265 m and chlorite + calcite appears implying the equilibrium 5 CaMg(CO₃)₂ + Al₂Si₂O₅(OH)₄ + SiO₂ + H₂OagMg₅Al₂Si₃O₁₀(OH)₈ + 5CaCO₃ + 5CO₂. (1)Equilibrium (1) involves CO₂ and H₂O which form an immiscible fluid at diagenetic conditions. Thermochemical data, activity coefficients for the fluid mixture (Margules solution model), and fugacity coefficients allow the position of intersection of the miscibility surface and equilibria similar to (1) to be calculated. Maximum temperatures (180–250°C) in water-rich fluids are in accord with geothermal gradients of 33°C/km and temperatures from vitrinite reflectance (220°C). It is suggested that produced CO₂ may be responsible for the development of secondary porosity during deep burial.