P–T–fO2 controls on a partly inverse chromite-bearing ultramafic intrusive: an evaluation from the Sukinda Massif, India

The chromites from the alpine type ultramafic intrusive of Sukinda, India, display a typical partly inverse spinel form and occur in two distinct zones: Brown Ore Zone (BOZ) and Grey Ore Zone (GOZ). The host ultramafites are mostly altered and are represented by the serpentinite, tremolite-talc(chlorite) schist, talc-serpentine schist and chlorite rock. The less altered variants are dunite, harzburgite and websterite. A dyke of orthopyroxenite runs through the main ultramafic body.The composition of olivine (Fo₉₂), orthopyroxene (En_92–89) and Al₂O₃ contents of the parental liquid (10.40–11.45%) determined from chromites, suggest that the parent melt is of boninitic affinity. The chemical plot of TiO₂ content against cr# of chromites corroborates a boninitic parental melt. The Fe–Mg partitioning in olivine and chromite depicts the temperature for chromitites as 1200 °C. A compositional plot of mg# and cr# suggests crystallization at high pressure conditions, corresponding to the kimberlite xenolith field. From the P–T diagram of pyrolite melting and mineral assemblage, the pressure of crystallization is stipulated to be ≥1.2 GPa. The f_O2 values estimated from Fe³⁺/Cr+Al+Fe³⁺ ratios range from 10^−8.3 to 10^−9.3 for the GOZ and 10^−7.1 to 10^−7.3 for the BOZ. The f_O2 values together with the pressure range suggest crystallization at upper mantle conditions. The heterogeneity in chemical composition and f_O2 conditions for the GOZ and BOZ could be linked to heterogeneity in the upper mantle.     

Fluid geochemistry of the Methana Peninsula and Loutraki geothermal area,Greece

A geochemical survey on the thermal fluids released by the volcanic/geothermal system of Methana Peninsula and Loutraki area was undertaken.     

Hydrogeochemistry and reservoir characterization of the Konya geothermal fields,Central Anatolia/Turkey

A conceptual model with water samples from ten geothermal fields (?smil, Ilg?n (Çavu?cugöl), Tuzlukçu-Ak?ehir, Seydi?ehir and Kavakköy, Hüyük, Ere?li-Akhüyük, Kad?nhan?, Cihanbeyli, Karap?nar and Bey?ehir) in the province of Konya defined the geothermal system. Carbonates, quartzite and marbles of Paleozoic metamorphics are the reservoir rocks and the heating sources are igneous rock intrusions and geothermal gradient. The variable thermal water (CaMgHCO₃, CaSO₄, NaSO₄, CaHCO₃, CaNaHCO₃, NaCl and CaNaClHCO₃) had EC and temperature between 177.8 and 56,100 μS/cm and between 18.3 and 44 °C, respectively. Ca²⁺ in geothermal fluids are associated with marble and carbonate rocks and the high chloride shows direct connection with deep geothermal system, and prolonged contact with evaporite rocks. Sulphate originates from dissolution of and oxidation of sulphate and sulphur-bearing minerals. The high As, B, F and Mn concentration in some thermal water samples were determined as 85 μg/l, 148.56 mg/l, 3.01 mg/l and 208.13 mg/l, respectively. Reservoir temperatures computed by Na/K geothermometers were between 85.37–158.89 °C for Ak?ehir thermal waters and 58.78–90.45 °C for Ere?li thermal waters. The maximum reservoir temperature of other geothermal waters was 75 °C by the silica geothermometers.     

Geochemistry and petrogenesis of the 595 Ma shoshonitic Qunai monzogabbro,Jordan

The last stage in the formation of the Arabian Nubian Shield in Jordan was dominated by post-orogenic igneous activity of the ∼610–542 Ma Araba Suite, including a monzogabbroic stock intruding the Saramuj Conglomerate, near the southeastern corner of the Dead Sea. The geological setting, petrography, geochemistry and geothermometry of the monzogabbro and other cogenetic varieties are used to shed light on the petrogenesis of this stock and reveal its magma source. The monzogabbro, megaporphyry dikes, and scattered syenite pockets are co-magmatic and alkaline, potassic and shoshonitic in nature. REE and trace elements patterns indicate that these magmas were produced from a mantle that had been modified by subduction-related metasomatism. The parental mafic magma could have been derived by 10% partial melting of LILE-enriched phlogopite-bearing spinel lherzolite, probably lithospheric mantle, in association with post-collisional extension. Fractional crystallization of this parental magma by olivine and pyroxene gave rise to the monzogabbroic magma.The megaporphyry dikes with their giant labradorite plagioclase megacrysts represent feeders of a voluminous volcanic activity that could have lasted for about 10⁵ years.Thermodynamic modeling applying the MELTS software indicates crystallization of this suite in the temperature range of 1184–760 °C at a pressure of 2 kbars, agreeing with olivine-pyroxene, pyroxene, and two-feldspar thermometry. The modeled mineralogy and sequence of crystallization of constituent minerals using MELTS is in remarkable agreement with the observed modal mineralogy of the monzogabbro. Furthermore, a great degree of congruity exists between the modeled and observed chemistry of the major minerals with only minor discrepancies between modeled composition of biotite and olivine.     

Temperature–time paths from phosphate accessory phase paragenesis in the Honey Brook Upland and associated cover sequence, SE Pennsylvania, USA

Analysis of monazite-bearing lithologies from the Precambrian Honey Brook Upland (HBU) and overlying metasedimentary Paleozoic Chester Valley Sequence (CVS) (SE PA, USA) reveals overprinting of primary major and accessory phase parageneses by texturally and compositionally disparate secondary accessory phase parageneses. Two-pyroxene temperatures of 915–945 °C for reconstituted pyroxene reflect emplacement temperatures of felsic plutonic rocks (opdalite, charnockite) prior to Mesoproterozoic metamorphism. Monazite in metavolcanic felsic gneiss yields three age domains at 1009 ± 4 Ma (2 s.e.), 965 ± 6, and 876 ± 10 Ma. The first two domains record metamorphism of the HBU after anorthosite intrusion; peak monazite–xenotime temperatures for the monazite core domain are 700 °C, and high Th/U values in the second (overgrowth) age domain likely reflect a second high-T monazite growth episode. Formation of cummingtonite coronas on orthopyroxene in opdalite constrains maximum 1010 Ma metamorphic temperatures in the “granulite-facies” terrane to 730–740 °C. Evidence of increased Cl fluid activity in the 965 Ma metamorphism includes higher Cl content of matrix apatite relative to garnet-included apatite (metavolcanics), and Cl-bearing K-hornblende succeeding cummingtonite in coronal overgrowths (opdalite). Extreme monazite Th/U values (75–250) in the rim domain suggest growth during low-T hydrothermal alteration. In the opdalite, secondary singe-grain monazite and monazite + xenotime metasomites in apatite yield ages of 714 ± 24 and 586 ± 88 Ma, temperatures of 325–425 °C, and are interpreted to reflect thermal disturbances associated with late Proterozoic plutonic and volcanic activity in the Upland. This thermal disturbance may be recorded by Rb–Sr age of 567 Ma for biotite from a HBU gneiss. Monazite age domains in metaquartzite (378 ± 28, 272 ± 44 Ma) suggest that low-grade metamorphism (260–320 °C, Mnz–Xno thermometry) of the CVS is not a result of Taconian orogenesis.     

Correlation of rhyolitic pyroclastic eruptive units from the Taupo volcanic zone by Fe–Ti oxide compositional data

Grain-specific analyses of Fe–Ti oxides and estimates of eruption temperature (T) and oxygen fugacity (fO₂) have been used to fingerprint rhyolitic fall and flow deposits that are important for tephrostratigraphic studies in and around the Taupo volcanic zone of North Island, New Zealand. The analysed Fe–Ti oxides commonly occur in the rims of orthopyroxene crystals and appear to reflect equilibrium immediately prior to eruption because of geochemical correlation with the co-existing glass phase. The composition of the spinel phase is particularly diagnostic of eruptive centre for post-65 ka events and can be used to distinguish many tephra beds from the same volcano. The 29 different units examined were erupted over a wide range in T (690–990°C) and Δ log fO₂ (–0.1 to 2.0). These parameters are closely related to the mafic mineral assemblage, with hydrous mineral-bearing units displaying higher fO₂. Such trends are superimposed on larger differences in fO₂ that are related to eruptive centre. At any given temperature, all post-65 ka Okataina centre tephra have higher fO₂ values than post-65 ka Taupo centre tephra. This provides a useful criterion for identifying the volcanic source. There are no temporal T and fO₂ trends in the tephra record; over intervals >20 ka, however, tephra sequences from Taupo centre form characteristic T-fO₂ buffer trends mirroring the glass chemistry. Individual eruptive events display uniform spinel and rhombohedral phase compositions and thus narrow ranges in T (± <20°C) and log fO₂ (± <0.5), allowing these features to identify individual magma batches. These criteria can help distinguish tephra deposits of similar bulk or glass composition that originated from the same volcano. Distal fall deposits record the same T-fO₂ conditions as the proximal ignimbrite and enable distal–proximal correlation. Lateral and vertical compositional and T-fO₂ variability displayed in large volume (>100 km³) ignimbrites, such as the Oruanui, Rotoiti and Ongatiti, is similar to that found in a single pumice clast and thus mainly reflects analytical error; however, thermal gradients of ca. 50°C may occur in some units. Received: 6 April 1998 / Accepted: 16 June 1998     

Hydrothermal alteration associated with rift zones at Fangataufa atoll (French Polynesia)

 The Mururoa and Fangataufa atoll basement consists of superimposed submarine and subaerial lava flows which have been intruded by late volcanics. The intrusions have developed large hydrothermal alteration haloes throughout the basaltic wall rock. The cuttings of the Natice-1 and Mitre-1 holes, drilled into the submarine volcanic pile at Fangataufa atoll, show a vertical zonation of clay minerals ranging from 270 to 850 m depth. The newly formed clay minerals occurring from top to bottom of the altered pile are: dioctahedral aluminous smectites, saponite, an intimate assemblage of saponite with two random chlorite/saponite mixed layers and an intimate assemblage of one random chlorite/saponite mixed-layer with one ordered chlorite/saponite mixed layer and one chlorite below 816 m depth. These clay mineral assemblages indicate a general increase in the chloritic component with depth. They are associated throughout the pile with secondary carbonates and quartz. The ∂¹⁸O and ∂¹³C of calcite and ∂¹⁸O of clay minerals, on the one hand, and the intimate mixtures of trioctahedral species, on the other, suggest a general cooling with the evolution of a paleogeothermal gradient from approximately 300  °C/km during the crystallization of chlorite to 150  °C/km for the late calcite precipitation. Received: 2 October 1995 / Accepted: 14 January 1997     

Recalibration of mutually consistent garnet–biotite and garnet–cordierite geothermometers

Garnet–biotite and garnet–cordierite geothermometers have been consistently calibrated, using the results of Fe²⁺–Mg cation exchange experiments and utilizing recently evaluated nonideal mixing properties of garnet. Nonideal mixing parameters of biotite (including Fe, Mg, Al^VI, and Ti) and of cordierite (involving Fe and Mg) are evaluated in terms of iterative multiple least-square regressions of the experimental results. Assuming the presence of ferric Fe in biotite in relation to the coexisting Fe-oxide phases (Case A), and assuming the absence of ferric Fe in biotite (Case B), two formulae of garnet–biotite thermometer have been derived. The garnet–cordierite geothermometer was constructed using Margules parameters of garnet adopted in the garnet–biotite geothermometers. The newly calibrated garnet–biotite and garnet–cordierite thermometers clearly show improved conformity in the calculated temperatures. The thermometers give temperatures that are consistent with each other using natural garnet–biotite–cordierite assemblages within ±50 °C. The effects of ferric Fe in biotite on garnet–biotite thermometry have been evaluated comparing the two calibrations of the thermometer. The effects are significant; it is clarified that taking ferric Fe content in biotite into account leads to less dispersion of thermometric results.     

Continuation of the San Andreas fault system into the upper mantle: Evidence from spinel peridotite xenoliths in the Coyote Lake basalt, central California

The Coyote Lake basalt, located near the intersection of the Hayward and Calaveras faults in central California, contains spinel peridotite xenoliths from the mantle beneath the San Andreas fault system. Six upper mantle xenoliths were studied in detail by a combination of petrologic techniques. Temperature estimates, obtained from three two-pyroxene geothermometers and the Al-in-orthopyroxene geothermometer, indicate that the xenoliths equilibrated at 970–1100 °C. A thermal model was used to estimate the corresponding depth of equilibration for these xenoliths, resulting in depths between 38 and 43 km. The lattice preferred orientation of olivine measured in five of the xenolith samples show strong point distributions of olivine crystallographic axes suggesting that fabrics formed under high-temperature conditions. Calculated seismic anisotropy values indicate an average shear wave anisotropy of 6%, higher than the anisotropy calculated from xenoliths from other tectonic environments. Using this value, the anisotropic layer responsible for fault-parallel shear wave splitting in central California is less than 100 km thick. The strong fabric preserved in the xenoliths suggests that a mantle shear zone exists below the Calaveras fault to a depth of at least 40 km, and combining xenolith petrofabrics with shear wave splitting studies helps distinguish between different models for deformation at depth beneath the San Andrea fault system.     

The metamorphic evolution of the high pressure mafic granulites of the Bacariza Formation (Cabo Ortegal Complex, Hercynian belt, NW Spain)

The high pressure mafic granulites of the Bacariza Formation outcrop in the two uppermost structural units of the Cabo Ortegal Complex (La Capelada unit and Cedeira unit) were separated by a Variscan thrust. In both cases, they appear as heterogeneous metabasites in normal contact between ultramafic rocks and other more homogeneous and less differentiated metabasic rocks, also affected by catazonal metamorphism. The main difference between the mafic granulites in the two units is the degree of deformation, which is higher in the underlying Cedeira unit. Petrologic and mineralogical data indicate that the high-pressure (HP) granulites (Gt-Cpx±Amp-Pl±Qtz±Scp-Rt±Ilm-Czo) are already retrograde (M2 Stage), post-dating an earlier eclogite facies metamorphism (M1 Stage) characterised by the mineral associations: Gt-Cpx±Amp±Ky±Qtz-Rt and Gt-Cpx±Amp±Qtz±Zo-Rt. The main structure related to the exhumation processes is the development of a general mylonitic foliation that, although initiated in granulite facies conditions, was mainly equilibrated in amphibolite facies (M3 Stage). This foliation was affected by isoclinal folds, which led to the formation of the Variscan thrusts responsible for the present stacking position. Thrust conditions were transitional between amphibolite and greenschist facies (M4 Stage). Thermobarometric data point to different P–T exhumation paths in the two units. Estimated P–T conditions were higher in La Capelada unit during M1 (P≥13 kbar; 860°C) and M2 (15 kbar; 800°C) than in the Cedeira unit (M1: P≥11 kbar, 770°C; M2: 12 kbar; 750°C). Temperatures for the M3 stage were comparable (720°C) in both units but rocks from the Cedeira unit show a much bigger drop in pressure. This resulted in an isothermal decompression type path for the Cedeira unit, while both P and T decreased more steadily in La Capelada rocks. These were always located at deeper level than the Cedeira rocks before the Variscan stacking. The difference in the two paths is related to different exhumation rates; higher in rocks from the Cedeira unit than in those from La Capelada. Exhumation processes coeval with underthrusting, and a different location of the rocks with respect to the main shear zone responsible for the exhumation would account for the distinct paths.