Petrology of the 1979 eruption of Soufriere volcano,St. Vincent,Lesser Antilles     

Alastair M. Graham  Matthew F. Thirlwall 《Contributions to Mineralogy and Petrology》1981,76(3):336-342

Major element, trace element, and Sr isotope data are used to study the temporal variation in the chemistry of the ejecta from the 1979 eruption of Soufriere volcano, St. Vincent, and to compare the compositions of the 1979 and 1971/2 magmas. Both the 1971/2 and 1979 products were basaltic andesites almost identical in petrography. A small temporal variation in chemistry is apparent in the 1979 samples but these cannot be related to the 1971/2 lava by fractional crystallisation of phenocryst phases, and the two eruptions may therefore have sampled different batches of magma. ⁸⁷Sr/⁸⁶Sr ratios of the two magmas were identical within analytical error.Microprobe analyses of phenocryst phases and glasses from the 1979 ejecta are presented. Clinopyroxene phenocryst cores with very high Mg/Fe ratios indicate that the basaltic andesites are products of fractionation of magnesian parents. Such magmas are represented by lavas on St. Vincent similar to the microphyric alkali picrites found to the south in Grenada. A common origin for the basaltic andesites of both islands by fractional crystallisation of picritic magmas is suggested. Dacitic glass is abundant in the groundmass of scoria blocks from the eruption. It does not represent the liquid originally in equilibrium with the phenocryst phases, but rather this liquid modified by quench crystallisation. Published interpretations suggesting that dacitic glass compositions in tephra from eruptions of the Soufriere are evidence of mixed-magma eruptions are therefore rejected.  相似文献   

Experimental hydrogen isotope studies III: Diffusion of hydrogen in hydrous minerals,and stable isotope exchange in metamorphic rocks   总被引：4，自引：0，他引：4  

Colin M. Graham 《Contributions to Mineralogy and Petrology》1981,76(2):216-228

Diffusion parameters for hydrogen diffusion in epidote-group minerals and micas have been measured under hydrothermal conditions, or calculated from existing experimental data, for bulk hydrogen isotope exchange experiments between hydrous minerals and water. Activation energies in the range 14 to 31 kcals/g-atom H are comparable to those derived by application of kinetic theory to experimental hydrogen isotope exchange data, and to those for oxygen diffusion in minerals under hydrothermal conditions. Diffusion of hydrogen in epidote is about four orders of magnitude faster than in muscovite, and about two orders of magnitude faster than in zoisite. Hydrogen diffusion in micas is about five orders of magnitude faster than oxygen diffusion, and hydrogen transport occurs dominantly parallel to the layers rather than parallel to the c-axis as for oxygen.Rapid hydrogen transport in minerals may proceed by hydrolysis of Si-O and Al-O bonds, followed by exchange of hydrolyzed oxygens with slower-diffusing (OH) or H₂O. Water appears to be essential for stable isotope exchange between minerals in slowly cooling metamorphic rocks.Stable isotope data for regional metamorphic mineral assemblages suggests that water is usually present in small amounts during cooling of prograde regional metamorphic systems, and estimated closure temperatures for cessation of stable isotope exchange are often more comparable to those calculated from diffusion data than to likely temperatures of metamorphism.Alpine deformation of the Hercynian Monte Rose Granite (Frey et al. 1976) permitted access of water and initiated stable isotope exchange amongst coexisting minerals. The diffusional behaviour of species in relict Hercynian muscovites is consistent with available experimental diffusion data.  相似文献   

Wrench faults,arcuate fold patterns and deformation in the southern French Alps     

R.H. Graham 《Proceedings of the Geologists' Association. Geologists' Association》1978,89(2):125-142

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Amino acid racemization dating of fossil bones,I. inter-laboratory comparison of racemization measurements     

Jeffrey L. Bada  E. Hoopes  D. Darling  Graham Dungworth  Henk J. Kessels  Keith A. Kvenvolden  David J. Blunt 《Earth and Planetary Science Letters》1979,43(2):265-268

Enantiomeric measurements for aspartic acid, glutamic acid, and alanine in twenty-one different fossil bone samples have been carried out by three different laboratories using different analytical methods. These inter-laboratory comparisons demonstrate that D/L aspartic acid measurements are highly reproducible, whereas the enantiomeric measurements for the other amino acids show a wide variation between the three laboratories. At present, aspartic acid measurements are the most suitable for racemization dating of bone because of their superior analytical precision.  相似文献   

Experimental hydrogen isotope studies,II. Fractionations in the systems epidote-NaCl-H₂O,epidote-CaCl₂-H₂O and epidote-seawater,and the hydrogen isotope composition of natural epidotes     

Colin M. Graham  Simon M.F. Sheppard 《Earth and Planetary Science Letters》1980,49(2):237-251

The hydrogen isotope fractionation factors between epidote and aqueous 1 M and 4 M NaCl, 1 M CaCl₂ solutions, and between epidote and seawater, have been measured over the temperature range 250–550°C over which the degree of dissociation of dissolved species varies significantly. Measured fractionations at 350°C are decreased by up to 12‰, 9‰ and 7‰ relative to pure water in seawater, 1 M CaCl₂ and 1 M NaCl respectively, while above 500°C fractionations are not measurably dependent on fluid composition. Water—solution fractionation factors are derived which are generally applicable to the correction of mineral—water hydrogen isotope fractionations for the composition of the fluid phase.The hydrogen isotope compositions of natural epidotes are interpreted in the light of experimental fractionation data for situations where temperature, δD (fluid), and, in some cases, fluid chemistry, are independently known. Epidotes from active geothermal systems have hydrogen isotope quench temperatures consistent with or close to measured well temperatures unless the measured temperature has declined substantially since epidote formation or there is uncertainty in the D/H ratio of the water associated with the epidote because of isotopic heterogeneity in the well waters. Hydrothermal and metamorphic epidotes show closure temperatures of 175–225°C and 200–250°C. There is no evidence that retrograde metamorphic fluids, if present, are isotopically different from prograde fluids.The water-solution fractionations indicate strong solute-solvent interactions between 250 and 450°C and imply that both dissociated and associated species contribute to the fractionation effects through modification of the orientations and structure of the water molecules. Solute-solvent interactions become negligible at temperatures around 550°C.  相似文献   

Spatial Variation in Nitrogen Isotope Values Beneath Nitrate Contamination Sources   总被引：8，自引：0，他引：8  

Graham E. Fogg  D.E. Rolston  D.L. Decker  D.T. Louie  M.E. Grismer 《Ground water》1998,36(3):418-426

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Crystallization of chromite from nickel-iron sulphide melts     

W. E. Ewers  J. Graham  D. R. Hudson  J. M. Rolls 《Contributions to Mineralogy and Petrology》1976,54(1):61-64

An experiment, in which an iron-nickel-copper sulphide melt was heated with synthetic chromite and then cooled, showed that substantial quantities of chromite had dissolved in the melt and had then recrystallized as euhedral crystals rimmed with magnetite. This experiment suggests that the unusual chromite (low in Mg and Al) which is associated with the sulphide phase in Western Australian nickel ores may have formed in a similar way.J.M.R. carried out the experimental part of this investigation as a post-graduate student at Flinders University, South Australia, working under a CSIRO extramural grant.  相似文献   

Lunar sample 15405: Remnant of a KREEP basalt-granite differentiated pluton     

Graham Ryder 《Earth and Planetary Science Letters》1976,29(2):255-268

Large, coarse-grained fragments of granite, containing plagioclase, a silica polymorph, potash feldspar, and exsolved pyroxene, with minor ilmenite, a phosphate, Fe-metal, and troilite, occur in sample 15405. A similar coarse-grained clast type (KREEP-rich quartz-monzodiorite) has a similar mineralogy but contains more ilmenite, large phosphates, less silica, and lacks troilite. One unusual KREEPy olivine vitrophyre fragment is also present. All the other fragments in 15405 are of Apollo 15-type KREEP basalt; ANT-suite and breccia fragments are conspicuously absent. The groundmass of 15405, of a KREEP basalt composition, is vesicular with a variolitic texture and is interpreted as an impact melt. Except for the olivine vitrophyre, the fragments are believed to be the remnants of a shallow-level KREEP basalt-granite differentiated pluton, in which granite was produced as the residual liquid without involvement of immiscibility effects.The large amount of melt required to produce the pluton, and the retention of the pluton's integrity from crystallization until the formation of the source boulder of 15405 suggest that KREEP basalt magma is not ancient (～4.3 b.y.), but was produced by the partial melting of the interior of the moon at around 3.90–3.95 b.y.; this conclusion is supported by the presence of KREEP basalt in soil breccia 15205, to the exclusion of other highland rock types. If this interpretation is correct, the source of Apollo 15-type KREEP basalt had a Rb/Sr ratio higher than anorthositic norite, commonly proposed as the source rock.  相似文献   

A rationale for the origins of massif anorthosites     

Graham Ryder 《Lithos》1974,7(3):139-146

The origin of massif anorthosites cannot be simply explained by a single magma type. Two of the commonly proposed parents for anorthosites are andesites (quartz-diorites) and high-alumina basalts. It is proposed here that these two magmas are the parents for two groups of anorthosites which include all anorthosite massifs, and that the parents for any given anorthosite massif can be determined by the rock sequence associated with the massif.Evidence from experiments and from phenocrysts in volcanics, suggests that andesites crystallizing in the granulite facies would produce plagioclase cumulates (anorthosites) at the base, followed by dioritic and acidic material, whereas high-alumina basalts would produce gabbros followed by anorthosite with very little succeeding acidic material. All massif anorthosites for which relevant data is available have one or the other of these stratigraphic sequences. Grouped according to these sequences, they coincide with two previously proposed groups, i.e. Andesine-type and Labradorite-type, whose characteristics are shown to be compatible with derivation from andesite and high-alumina basalt, respectively.  相似文献   

Resolved spectroscopy of a gravitationally lensed L* Lyman-break galaxy at z∼ 5     

A. M. Swinbank  R. G. Bower  Graham P. Smith  R. J. Wilman  Ian Smail  R. S. Ellis  S. L. Morris  J.-P. Kneib 《Monthly notices of the Royal Astronomical Society》2007,376(2):479-491

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