Garnet and clinopyroxene solid solutions,and geothermometry based on Fe-Mg distribution coefficient

The available thermodynamic mixing data of aluminosilicate garnet and clinopyroxene have been critically reviewed, and integrated with the thermochemical and selected experimental data to express the Fe-Mg distribution coefficient (K_D) between these phases as function of pressure, temperature and composition. The predicted compositional dependence of K_D agrees with the available experimental and observational data. Owing to the lack of adequate data on the mixing properties of Jadeite with diopside and hedenbergite, the geothermometric application of the model has to be currently restricted to the Na-poor bulk compositions. The temperature of a variety of rocks that have equilibrated under a wide range of P-T conditions have been estimated, and found to agree, on the average within 25°C, with other reliable temperature estimates of these rocks. The latter are, however, often in sharp disagreement with the temperatures determined on the basis of Råheim and Green's (1974, Contrib. Mineral. Petrol.48, 179–203) experimental calibration of K_D as function of temperature and pressure on tholeiitic bulk composition.     

Multistage melt impregnation in Tethyan oceanic mantle: Petrochemical constraints from channelized melt flow in the Naga Hills Ophiolite

Ophiolitic sequences obducted onto continental margins allow field based observations coupled with petrochemical interrogations of upper mantle lithologies thereby aiding evaluation of compositional heterogeneity of oceanic mantle, depletion-enrichment events and geodynamic conditions governing oceanic lithosphere formation. The Naga Hills Ophiolite (NHO) suite preserves a segment of the Neotethyan oceanic lithosphere encompassing a package of mantle and crustal lithologies. This paper for the first time reports the occurrence of melt flow channels traversing the mantle section near Molen of the NHO and presents a comprehensive study involving chromite-spinel chemistry, bulk rock major, trace and PGE geochemistry to understand the petrogenesis and evolution in a geodynamic transition from mid oceanic ridge (MOR) to suprasubduction zone (SSZ). The spinel chemistry of peridotitic melt channels depicts both MOR-type and SSZ signatures underlining a transitional tectonic frame. Chromite chemistry and high Al₂O₃/TiO₂ ranging from 15.98–35.70 in concurrence with low CaO/Al₂O₃ ranging from 0.03–0.53; and chondrite normalised LREE > MREE < HREE patterns confirm the influx of boninitic melts into the refractory mantle. The boninitic signature shared by melt channels and host rock invokes a geochemical and geodynamic transition from anhydrous melting of depleted mantle to hydrated fluid flux melting resulting in boninitic melts, that subsequently impregnate and refertilise the fore arc mantle wedge in a SSZ regime at the nascent stage of subduction. The high Ba/Nb, Ba/Th, and Ba/La for the studied peridotites highlight the influx of subduction derived fluids in the supra subduction mantle. Further higher Zr/Hf and Nd/Hf with respect to primitive mantle values in concurrence with lower Nb/Ta suggest progressive refertilisation due to fluid- and melt-driven metasomatism of the refractory fore arc mantle wedge. The chondrite normalised PGE patterns suggest positive Ir and Ru anomalies stipulating the source to be refractory while enriched Pt and Pd underpins the mobilisation of these elements by subduction derived fluids and melts. The elevated abundances of PPGEs than IPGEs as cited by PPGE/IPGE > 1; and Pd/Pt avg. 0.85 for melt channels and 0.84 for host peridotites indicate fluid-fluxed metasomatism of fore arc mantle wedge with a S-undersaturated trend coupled with boninitic affinity. The mineral, trace, REE and PGE chemistry collectively emphasizes that the mantle peridotites of the NHO formed in a transitional geodynamic tectonic setting caused by fore arc extension during subduction initiation followed by rejuvenation by subduction derived fluids and boninitic melts, which typically are of the SSZ tectonic regime. The harzburgitic melt channels and host rock are refractory in nature, reflecting multiple episodes of melt extraction of about 5–15% and ~10–20% respectively from a spinel peridotite mantle source. The occurrences of these melt channels indicate segregation and percolation of melt through porous and channelized network in upper mantle peridotites.     

Aluminous orthopyroxene: Order-disorder,thermodynamic properties,and petrologic implications

Orthopyroxene has two tetrahedral sites, designated A and B, and two octahedral sites, M1 and M2. Crystallographic studies of synthetic and natural orthopyroxenes (opx) suggest that the tetrahedral Al is ordered nearly completely in the B site, but the octahedral Al disorders between M1 and M2 sites with a preference for M1. If the aluminum avoidance principle is obeyed, then the tetrahedral Si-Al ordering limits the Al substitution in opx to 25 mol%, thus leading to an end-member stoichiometry of Mg₃Al₂Si₃O₁₂ instead of MgAl₂SiO₆.The enthalpy of formation of these two components has been deduced from the available phase equilibrium data. The thermodynamic properties of the opx solid solution approximates ideal solution behavior more closely when treated in terms of the components Mg₄Si₄O₁₂(QEn)-Mg₃Al₂Si₃O₁₂(Py) than when expressed in terms of the components Mg₂Si₂O₆-MgAl₂SiO₆. A model has been developed for the octahedral disordering of Al as function of temperature and composition. These data enable calculation of the configurational entropy and molar entropy of Al-opx; distinction has been made between the cases of completely random mixing of Al and Si in the tetrahedral B site, and of random mixing without violation of the aluminum avoidance principle. The second model yields entropy of the Mg₃Al₂Si₃O₁₂ end member which agrees almost exactly with the value derived from phase equilibrium data. The partial molal entropies of the Orthopyroxene components QEn and Py can be derived from these data; their implications with respect to the P-T slopes of Al₂O₃ isopleths for the equilibrium of Orthopyroxene with forsterite and spinel/garnet have been discussed.     

Tectono-magmatic evolution of Tethyan oceanic lithosphere in supra subduction zone fore arc regime: Geochemical fingerprints from crust-mantle sections of Naga Hills Ophiolite

The Naga Hills Ophiolite(NHO) belt in the Indo-Myanmar range(IMR) represents a segment of Tethyan oceanic crust and upper mantle that was involved in an eastward convergence and collision of the Indian Plate with the Burmese Plate during the Late Cretaceous-Eocene.Here, we present a detailed petrological and geochemical account for the mantle and crustal sections of NHO, northeastern India to address(i) the mantle processes and tectonic regimes involved in their genesis and(ii) their coherence in terms of the thermo-tectonic evolution of Tethyan oceanic crust and upper mantle.The NHO suite comprises well preserved crustal and mantle sections discretely exposed at Moki, Ziphu, Molen, Washelo and Lacham areas.The ultramafic-mafic lithologies of NHO are mineralogically composed of variable proportions of olivine, orthopyroxene, clinopyroxene and plagioclase.The primary igneous textures for the mantle peridotites have been overprinted by extensive serpentinisation whereas the crustal section rocks reflect crystal cumulation in a magma chamber.Chondrite normalised REE profiles for the cumulate peridotite-olivine gabbro-gabbro assemblage constituting the crustal section of NHO show flat to depleted LREE patterns consistent with their generation from depleted MORB-type precursor melt in an extensional tectonic setting, while the mantle peridotites depict U-shaped REE patterns marked by relative enrichment of LREE and HREE over MREE.These features collectively imply a dual role of depleted MORB-type and enriched arc-type mantle components for their genesis with imprints of melt-rock and fluid-rock interactions.Tectonically, studied lithologies from NHO correspond to a boninitic to slab-proximal Island Arc Tholeiite affinity thereby conforming to an intraoceanic supra subduction zone(SSZ) fore-arc regime coherent with the subduction initiation process.The geochemical attributes for the crustal and mantle sections of NHO as mirrored by Zr/Hf, Zr/Sm, Nb/Ta, Zr/Nb, Nb/U, Ba/Nb, Ba/Th, Ba/La and Nd/Hf ratios propound a two-stage petrogenetic process:(i) a depleted fore arc basalt(FAB) type tholeiitic melt parental to the crustal lithologies was extracted from the upwelling asthenospheric mantle at SSZ fore-arc extensional regime thereby rendering a refractory residual upper mantle;(ii) the crust and upper mantle of the SSZ fore arc were progressively refertilised by boninitic melts generated in response to subduction initiation and slab-dehydration.The vestiges of Tethyan oceanic lithosphere preserved in NHO represent an accreted intra-oceanic fore arc crust and upper mantle section which records a transitional geodynamic evolution in a SSZ regime marked by subduction initiation, fore arc extension and arc-continent accretion.     

Thermodynamics of aluminosilicate garnet solid solution: new experimental data,an optimized model,and thermometric applications

 We have experimentally determined the displacement of the equilibrium Grossular + 2 Kyanite + Quartz ⇆ 3 Anorthite (GASP) as a function of garnet composition in the systems Mg-Ca-Mn, Fe-Mg-Ca and Fe-Mg-Ca-Mn at 1000°C. The results were treated along with selected experimental and observational data available in the literature as well as binary parameters from other workers to obtain a set of mutually compatible binary mixing parameters of the quaternary (Fe,Mg,Ca,Mn)- aluminosilicate garnet solid solution. Attempts to determine equilibrium garnet composition in the GASP equilibrium in the Ca-Mg binary were unsuccessful due to the formation of pyroxene. Calculations of binary and ternary miscibility gaps show that the P,T,X combination required for unmixing of garnet solid solution is not realized by natural samples. The solution model was applied to account for compositional effects on Fe-Mg exchange between garnet and ortho- or clino-pyroxene. Applications of the revised thermometric formulations to selected natural assemblages yield P-T conditions which are much less sensitive to compositional effects compared to the other available formulations, and are consistent with independent constraints. Received: 21 April 1995 / Accepted: 17 May 1996     

Extensional collapse of the Gondwana orogen: Evidence from Cambrian mafic magmatism in the Trivandrum Block,southern India

The assembly of Late Neoproterozoice Cambrian supercontinent Gondwana involved prolonged subduction and accretion generating arc magmatic and accretionary complexes, culminating in collision and formation of high grade metamorphic orogens. Here we report evidence for mafic magmatism associated with post-collisional extension from a suite of gabbroic rocks in the Trivandrum Block of southern Indian Gondwana fragment. Our petrological and geochemical data on these gabbroic suite show that they are analogous to high Fe tholeiitic basalts with evolution of the parental melts dominantly controlled by fractional crystallization. They display enrichment of LILE and LREE and depletion of HFSE with negative anomalies at Zre Hf and Ti corresponding to subduction zone magmatic regime. The tectonic affinity of the gabbros coupled with their geochemical features endorse a heterogeneous mantle source with collective melt contributions from sub-slab asthenospheric mantle upwelling through slab break-off and arc-related metasomatized mantle wedge, with magma emplacement in subduction to post-collisional intraplate settings. The high Nb contents and positive Nbe Ta anomalies of the rocks are attributed to inflow of asthenospheric melts containing ancient recycled subducted slab components and/or fusion of subducted slab materials owing to upwelling of hot asthenosphere. Zircon grains from the gabbros show magmatic crystallization texture with low U and Pb content. The LA-ICPMS analyses show ²⁰⁶ Pb/²³⁸ U mean ages in the range of 507-494 Ma suggesting Cambrian mafic magmatism. The post-collisional mafic magmatism identified in our study provides new insights into mantle dynamics during the waning stage of the birth of a supercontinent.     

The energetics of natural garnet solid solution

Approximate mixing properties of the dominant calcium silicate end-member components of natural garnets, namely grossularite, andradite and uvarovite, have been derived through theoretical thermodynamic and crystal chemical analysis, and appropriate reduction of the available experimental data. The stability of the solid solution with respect to phase separation in the ternary system has been analyzed. Finally, a general model is presented as to the approximate mixing properties of multicomponent natural garnet solid solution involving substitutions in both eight and six coordinated sites.     

Mineralogical study of gabbro-anorthosite from Dumka, Chhotanagpur Gneissic Complex, Eastern Indian Shield

The Chhotanagpur Gneissic Complex (CGC), bearing imprints of widespread high grade metamorphic and magmatic history since Palaeoproterozoic, represents an integral crustal segment of Eastern Indian Shield. The gabbroanorthosite intrusives constitute a part of mafic-ultramafic magmatism in the CGC. The study area around Dumka (24°16?? to 24°20??N: 87°13?? to 87°22??E) predominantly comprises of granite gneiss and charnockitic country rocks within which gabbro-anorthosite intrusions occur as lenses. Field relations and structural studies reveal that the country rocks of Dumka have suffered three phases of deformation represented by F₁, F₂ and F₃ folds. The gabbro-anorthosite intrusives maintain a sharp contact with the host rocks, deformed and metamorphosed. Relict igneous layering or primary igneous foliation (S_ig) is recorded where metamorphic overprint is minimal. Mineral phases of gabbro-anorthosite rocks suggest that clinopyroxene compositions from gabrro correspond to diopside and clinoferrosilite, while those from anorthosite are clinoferrosilite. Amphiboles from the gabbro-anorthosite rocks are calcic, and range from ferroan pargasite in gabbro to ferroan pargasitic hornblende in anorthosite. Plagioclase from gabbro and anorthosite belong to bytownite and andesine respectively. Chemical composition of garnet in gabbro is almandine. Thermobarometric estimates for Dumka gabbroanorthosites correspond to 511°C to 915°C and 5.0?C7.5 kb pressure, comparable to that estimated for Bengal Anorthosite (593?C795°C, 4.1?C7.3 kb). Fractionation trend of plagioclase substantiates a single parental magma in the evolution of Dumka gabbro-anorthosite intrusives.     

Comparative Analysis of Phytoplankton Composition and Abundance over a Two-Decade Period at the Land–Ocean Boundary of a Tropical Mangrove Ecosystem

Inter-annual variations of phytoplankton abundance and community organization were observed over a two-decade period along with the ancillary parameters at the land–ocean boundary associated with the Sundarban mangrove forest (21°32′ and 22°40′ N and 88°05′ and 89° E), along the NE Coast of the Bay of Bengal. The number of definable Bacillariophyceae species exceeded Dinophyceae taxa, and the total number of bloom-forming species declined from a maximum of ten in 2000 and a minimum of two in 2007. Blooms of the diatom Coscinodiscus radiatus were common in 2000 and 2007. Tide cycles and the onset of the monsoon season played important roles in diurnal and seasonal variability of phytoplankton. Phytoplankton biovolume showed seasonality, with the highest levels during post-monsoon periods and lowest levels during the monsoon period. Phytoplankton abundance was correlated to rainfall patterns, which may be altered by long-term changes in climate.     

Anomalous behaviour of uranium isotopes in coastal marine environment of the west coast of India

During the last few years, a remarkable anomaly between ²³⁸U and ²³⁴U activities has been observed in the top layers of the coastal sediments along the western region of the Indian sub-continent. Sediment samples from Bombay (19°N, 73°E) to Kottilppad (8°N, 77°E) were leached with saturated ammonium carbonate solution to extract uranium isotopes from the surface layers of the sediment particles without attacking the mineral cores. The ²³⁴U/²³⁸U activity ratios in these leachates are in the range of 1.12–1.14 while ²³⁵U/²³⁸U activity ratio is 0.046 which is the same as for other natural uranium.

The surface organic matter from the sediment particles was removed by treatment with hydrogen peroxide in presence of 0.05 M hydrochloric acid. ²³⁴U/²³⁸U and ²³⁵u/²³⁸U activity ratios in the extract and the residues were determined.

It is observed that disequilibrium between ²³⁸U and ²³⁴U exists only on the surface of sediment particles. ²³⁴U/²³⁸U on the surface of the sediment particles is the same as in the ambient water and as the surface organic matter is removed from the particle surface, the cores show equilibrium activities.