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Notes: [Auszug] Granovsky1'4 suggested that leaf hoppers produced injury by introducing some chemical or enzymatic toxin into the plant with their salivary secretions. Histological and chemical studies by Smith and Poos5 and Smith6 demonstrated that feeding leaf hoppers injected a protein aceous sheath material ...

Notes: [Auszug] A piston-cylinder apparatus was used for generating high pressures. In this device, a, tungsten carbide piston advances into a 'Carboloy' high-pressure chamber 0-5 in. in diameter and 2 in. long. The sample was sealed in a length of platinum tubing, i in. x £ in., which was placed inside the ...

Notes: The Shevaroy Hills of northern Tamil Nadu, southern India, expose the highest-grade granulites of a prograde amphibolite facies to granulite facies deep-crustal section of Late Archaean age. These highly oxidized quartzofeldspathic garnet charnockites generally show minor high-TiO2 biotite and amphibole as the only hydrous minerals and are greatly depleted in the incompatible elements Rb and Th. Peak metamorphic temperatures (garnet–orthopyroxene) and pressures (garnet–orthopyroxene–plagioclase–quartz) are near 750 °C and 8 kbar, respectively. Pervasive veinlets of K-feldspar exist throughout dominant plagioclase in each sample and show clean contact with orthopyroxene. They are suggested to have been produced by a low H2O activity, migrating fluid phase under granulite facies conditions, most likely a concentrated chloride/carbonate brine with high alkali mobility accompanied by an immiscible CO2-rich fluid. Silicate, oxide and sulphide mineral assemblages record high oxygen fugacity. Pyroxenes in the felsic rocks have high Mg/(Mg+Fe) (0.5–0.7). The major oxide mineral is ilmenite with up to 60 mole per cent exsolved hematite. Utilizing three independent oxygen barometers (ferrosilite–magnetite–quartz, ferrosilite–hematite–quartz and magnetite–hematite) in conjunction with garnet–orthopyroxene exchange temperatures, samples with XIlmHm〉0.1 yield a consistent oxygen fugacity about two log units above fayalite stability. Less oxidized samples (XIlmHm〈0.1) show some scatter with indications of having equilibrated under more reducing conditions. Temperature-f (O2 ) arrays result in self consistent conditions ranging from 660 °C and 10−16 bar to 820 °C and 10−11.5 bar. These trends are confirmed by calculations based on the assemblage clinopyroxene–orthopyroxene–magnetite–ilmenite using the QUIlF program. In the most oxidized granulite samples (XIlmHm〉0.4) pyrite is the dominant sulphide and pyrrhotite is absent. Pyrite grains in these samples have marginal alteration to magnetite along the rims, signifying a high-temperature oxidation event. Moderately oxidized samples (0.1〈XIlmHm〈0.4) have abundant co-existing pyrrhotite, pyrite and magnetite. The most reduced granulite samples have pyrrhotite as the dominant sulphide with little or no pyrite and no coexisting magnetite. Chalcopyrite is a common accessory mineral of pyrite and pyrrhotite in all the samples. Textures in some samples suggest that it formed as an exsolution product from pyrrhotite. Extensive vein networks of magnetite and pyrite, associated principally with the pyroxene and amphibole, give evidence for a pervasive, highly oxidizing fluid phase. Thermodynamic analysis of the assemblage pyrrhotite, pyrite and magnetite yields consistent high oxidation states at 700–800 °C and 8 kbar. The oxygen fugacity in our most oxidized pyrrhotite-bearing sample is 10−12.65 bar at 770 °C. There are strong indications that the Shevaroy Hills granulites recrystallized in the presence of an alkali-rich, low H2O-activity fluid, probably a concentrated brine. It cannot be demonstrated at present whether the high oxidation states were set by initially oxidized protoliths or effected by the postulated fluids. The high correspondence of maximally Rb-depleted samples with the highest recorded oxidation states suggests that the Rb depletion event coincided with the oxidation event, probably during breakdown of biotite to orthopyroxene+K-feldspar. We speculate that these alterations were effected by exhalations from deep-seated alkali basalts, which provided both heat and high oxygen fugacity, low aH2O fluids. It will be of interest to determine whether greatly Rb-depleted granulites in other Precambrian terranes show similar highly-oxidizing signatures.

Notes: Abstract Fluid inclusion studies of rocks from the late Archaean amphibolite-facies to granulite-facies transition zone of southern India provide support for the hypothesis that CO2,-rich H2O-poor fluids were a major factor in the origin of the high-grade terrain. Charnockites, closely associated leucogranites and quartzo-feldspathic veins contain vast numbers of large CO2-rich inclusions in planar arrays in quartz and feldspar, whereas amphibole-bearing gray gneisses of essentially the same compositions as adjacent charnockites in mixed-facies quarries contain no large fluid inclusions. Inclusions in the northernmost incipient charnockites, as at Kabbal, Karnataka, occasionally contain about 25 mol. % of immiscible H2O lining cavity walls, whereas inclusions from the charnockite massif terrane farther south do not have visibile H2OMicrothermometry of CO2 inclusions shows that miscible CH4 and N2 must be small, probably less than 10mol.%combined. Densities of CO2 increase steadily from north to south across the transitional terrane. Entrapment pressures calculated from the CO2 equation of state range from 5 kbar in the north to 7.5 kbar in the south at the mineralogically inferred average metamorphic temperature of 750°C, in quantitative agreement with mineralogic geobarometry. This agreement leads to the inference that the fluid inclusions were trapped at or near peak metamorphic conditions.Calculations on the stability of the charnockite assemblage biotite-orthopyroxene-K-feldspar-quartz show that an associated fluid phase must have less than 0.35 H2O activity at the inferred P and T conditions, which agrees with the petrographic observations. High TiO2 content of biotite stabilizes it to lower H2O activities, and the steady increase of biotite TiO2 southward in the area suggests progressive decrease of aH2O with increasing grade. Oxygen fugacities calculated from orthopyroxene-magnetite-quartz are considerably higher than the graphite CO2-O2 buffer, which explains the absence of graphite in the charnockites.The present study quantifies the nature of the vapours in the southern India granulite metamorphism. It remains to be determined whether CO2-flushing of the crust can, by itself, create large terranes of largeion lithophile-depleted granulites, or whether removal of H2O-bearing anatectic melts is essential.

Notes: Charnockitic alteration (arrested orthopyroxene formation in biotite- and amphibole-bearing rocks) occurs in high-grade terranes of all ages. Three criteria are used to show that this alteration was produced in many locations by a migrating fluid phase: (i) diffuseness of the alteration—the alteration zones are often quite unlike discrete migmatitic veins; (ii) relation to deformation—most occurrences show alteration closely associated with warping of foliation or dilation cracks; (iii) open-system alteration—whilst some occurrences represent nearly isochemical alteration, slight changes in bulk composition, often loss of mafic constituents and gain of Na and Si, are evident in detailed mass-balance analysis. Y and sometimes Rb are characteristically depleted. Partial melting sometimes accompanied volatile infiltration, as evidenced by more discrete veins and euhedral orthopyroxene. It is quite unlikely, however, that open-system alteration was produced by escape of viscous quartzo-feldspathic melts. Pervasive migration of low-T lamprophyric (mafic–alkaline, CO2-charged) interstitial liquids is a possibility by virtue of their extreme fluidity, but CO2 infiltration was needed to generate these liquids. Vapour-deficient dehydration melting is another feasible mechanism of orthopyroxene formation which may have operated in conjunction with CO2 infiltration.Characteristic development of charnockitic alteration in some prograde amphibolite to granulite facies transitions, as in the Dharwar Craton of South India, suggests that the alteration is a fundamental feature of the granulite facies metamorphism, implying active and causal participation of migrating fluids. In other high-grade terranes like the Adirondack Mountains of New York, this kind of alteration is rare, and fluid action does not seem to have been important in the metamorphism.A vapour phase participating in charnockitic metamorphism was necessarily one of relatively low H2O, therefore presumably rich in CO2. Consideration of possible large CO2 sources leads to the conclusion that emanations from volatile-rich basalts emplaced in the lower crust are the most probable source of charnockitizing fluids. The ultimate source would therefore be enriched subcontinental lithosphere or asthenosphere. The Rb-depleted pyroxene gneiss (charnockitic) terranes may be characteristic of zones of large-scale transcurrent or oblique-motion faults which tap such great depths.

Notes: Abstract The enthalpy of reaction of plagioclase and pyroxene to produce garnet and quartz has been a major source of error in granulite geobarometry because of relatively uncertain enthalpy values available from high-temperature solution calorimetry and compiled indirectly from experimental phase equilibria. Recent, improved calorimetric measurements of ΔHR are shown to yield palaeopressures which are internally consistent between orthopyroxene and clinopyroxene calibrations for many South Indian granulites from the Archaean high-grade terranes of southern Karnataka and northern Tamil Nadu. This represents a considerable improvement over previous calibrations, which gave disparate results for the two independent barometers involving orthopyroxene and clinopyroxene, requiring a 2-kbar ‘empirical adjustment’to force agreement.Palaeopressures thus calculated for 30 well-documented two-pyroxene garnet granulites from South India give internally consistent pressures with a mean of 8.1°1.1 kbar at 750°C, consistent with the presence of both kyanite and sillimanite in many areas. Those samples for which garnet–pyroxene exchange thermometers give plausible granulite-range temperatures and whose minerals are minimally zoned give the best agreement of the two barometers. Samples which yield low palaeotemperatures and different rim and core compositions of minerals yield pressures for the orthopyroxene assemblage as much as 2 kbar lower than for the assemblage with clinopyroxene. This disparity probably represents post-metamorphic-peak re-equilibration. We conclude that considerable confidence may be placed in geobarometry of two-pyroxene granulites where apparent palaeotemperatures are in the granulite facies range (〉700°C) and where mineral zonation is minimal. Of the several possible sets of activity–composition relations in use, those constructed from analysis of phase equilibria give slightly higher palaeopressures and appear more consistent with analytical data from the Nilgiri Hills uplift, where kyanite is the only aluminium silicate reported to be stable in peak-metamorphic assemblages. The present results support a palaeopressure gradient, increasing generally from south to north, across the Nilgiri Hills as inferred by previous geobarometry.