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At least 667 records · Page 37Linked to original sources
USGS1986

Partition coefficients of Hf, Zr, and REE between zircon, apatite, and liquid

Concentration ratios of Hf, Zr, and REE between zircon, apatite, and liquid were determined for three igneous compositions: two andesites and a diorite. The concentration ratios of these elements between zircon and corresponding liquid can approximate the partition coefficient. Although the concentration ratios between apatite and andesite groundmass can be considered as partition coefficients, those for the apatite in the diorite may deviate from the partition coefficients. The HREE partition coefficients between zircon and liquid are very large (100 for Er to 500 for Lu), and the Hf partition coefficient is even larger. The REE partition coefficients between apatite and liquid are convex upward, and large (D=10-100), whereas the Hf and Zr partition coefficients are less than 1. The large differences between partition coefficients of Lu and Hf for zircon-liquid and for apatite-liquid are confirmed. These partition coefficients are useful for petrogenetic models involving zircon and apatite. ?? 1986 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1989

Geochemistry of intrusive rocks associated with the Latir volcanic field, New Mexico, and contrasts between evolution of plutonic and volcanic rocks

Plutonic rocks associated with the Latir volcanic field comprise three groups: 1) ???25 Ma high-level resurgent plutons composed of monzogranite and silicic metaluminous and peralkaline granite, 2) 23-25 Ma syenogranite, and alkali-feldspar granite intrusions emplaced along the southern caldera margin, and 3) 19-23 Ma granodiorite and granite plutons emplaced south of the caldera. Major-element compositions of both extrusive and intrusive suites in the Latir field are broadly similar; both suites include high-SiO2 rocks with low Ba and Sr, and high Rb, Nb, Th, and U contents. Moreover, both intermediateto siliciccomposition volcanic and plutonic rocks contain abundant accessory sphene and apatite, rich in rare-earth elements (REE), as well as phases in which REE's are essential components. Strong depletion in Y and REE contents, with increasing SiO2 content, in the plutonic rocks indicate a major role for accessory mineral fractionation that is not observed in volcanic rocks of equivalent composition. Considerations of the rheology of granitic magma suggest that accessory-mineral fractionation may occur primarily by filter-pressing evolved magmas from crystal-rich melts. More limited accessory-mineral crystallization and fractionation during evolution of the volcanic magmas may have resulted from markedly lower diffusivities of essential trace elements than major elements. Accessory-mineral fractionation probably becomes most significant at high crystallinities. The contrast in crystallization environments postulated for the extrusive and intrusive rocks may be common to other magmatic systems; the effects are particularly pronounced in highly evolved rocks of the Latir field. High-SiO2 peralkaline porphyry emplaced during resurgence of the Questa caldera represents non-erupted portions of the magma that produced the Amalia Tuff during caldera-forming eruption. The peralkaline porphyry continues compositional and mineralogical trends found in the tuff. Amphibole, mica, and sphene compositions suggest that the peralkaline magma evolved from metaluminous magma. Extensive feldspar fractionation occurred during evolution of the peralkaline magmas, but additional alkali and iron enrichment was likely a result of high halogen fluxes from crystallizing plutons and basaltic magmas at depth. ?? 1989 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1984

Comparative geochronology in the reversely zoned plutons of the Bottle Lake Complex, Maine: U-Pb on zircons and Rb-Sr on whole rocks

The Bottle Lake Complex is a composite granitic batholith emplaced into Cambrian to Lower Devonian metasedimentary rocks. Both plutons (Whitney Cove and Passadumkeag River) are very coarse grained hornblende and biotite-bearing granites showing petrographic and geochemical reverse zonation. Two linear whole rock Rb/Sr isochrons on xenolith-free Whitney Cove and Passadumkeag River samples indicate ages of 379??5 m.y. and 381??4 m.y., respectively, in close agreement with published K-Ar ages for biotite from Whitney Cove of 377 m.y. and 379 m.y., and for hornblende 40Ar/39Ar determinations from Passadumkeag River which indicate an age of 378??4 m.y. The initial Sr isotopic ratio for Whitney Cove is 0.70553 and for Passadumkeag River is 0.70414. A whole-rock isochron on a suite of xenoliths from the Passadumkeag River granite indicates a whole rock Rb-Sr age of 496??14 m.y., with an initial Sr isotopic ratio of 0.70262. Two types of zircon exhibiting wide petrographic diversity are evident in variable proportions throughout the batholith. One of these types is preferentially found in a mafic xenolith and it is widely dispersed in the host granites forming discrete grains and probably as inclusions in the other type of zircon. U-Pb analyses of zircons give concordia intercept ages of 399??8 m.y. for Whitney Cove, 388??6 m.y. for Passadumkeag River, 415 m.y. for a mafic xenolith in Passadumkeag River, and 396??32 for combined Whitney Cove and Passadumkeag River granite. The zircons show a spread of up to 20 m.y. in the 207Pb/206Pb ages. Omitting the finest zircon fraction in the Passadumkeag River results in a concordia intercept age of 381??3 m.y., in better agreement with the whole-rock Rb-Sr and mineral K-Ar ages. For the Whitney Cove pluton, exclusion of the finest fraction does not bring the zircon age into agreement with the Rb-Sr data. Age estimates by the whole rock Rb-Sr, mineral K-Ar and Ar-Ar methods suggest that the crystallization age of the plutons is about 380 m.y., slightly younger than the U-Pb zircon intercept ages. A possible reason for this discrepancy is that the zircons contain inherited lead. Thus, zircon U-Pb ages might represent a mixture of newly developed zircon and older inherited zircon, whereas the Rb-Sr whole rock age (380 m.y.) reflects the time of crystallization, and the argon ages result from rapid cooling after emplacement. ?? 1984 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1969

A Rubidium-Strontium study of the Twilight Gneiss, West Needle Mountains, Colorado

The Precambrian trondhjemitic Twilight Gneiss (Twilight Granite of CROSS and HOWE , 1905b) of the West Needle Mountains, southwestern Colorado, and its interlayered amphibolite and metarhyodacite yield a Rb-Sr isochron of 1,805±35 m.y. A low initial Sr 87 /Sr 86 ratio of 0.7015 implies that metamorphism of these rocks to amphibolite facies took place soon after their emplacement. The mild metamorphism of Uncompahgran age, prior to 1,460 m.y. ago, and Laramide volcanism did not affect the Rb-Sr system in the Twilight. Rb contents of 26.5 to 108 ppm, Sr contents of 114 to 251 ppm, and K 2 O percentages of 1.23 to 3.64 in the Twilight Gneiss, in conjunction with high K/Rb ratios and the low initial ratio of Sr 87 /Sr 86 , lend support to geologic data that suggest the Twilight originated as volcanic or hypabyssal igneous rocks in a basaltic volcanic pile.

Colorado↗
USGS1982

Age and origin of the Cortlandt Complex, New York: Implications from Sm-Nd data

Sm-Nd systematics for nine whole-rock samples of hornblende norites, pyroxenites and a lamprophyre from various parts of the Cortlandt Complex were analyzed. Six of these samples from the central and eastern parts of the complex give an isochron age of 430??34 (2 ??) Ma with an e{open}Nd value of -2.9??0.5, and the other three samples from the western part, including the lamprophyre, define a similar age of 394??33 (2 ??) Ma but with a distinctly different e{open}Nd value of -1.4??0.4. The two different initial 143Nd/144Nd ratios corresponding to these e{open}-values are interpreted to reflect continental crustal contamination of the lamprophyric parental liquid prior to final emplacement and crystal fractionation to produce the different rock types of the complex. The intrusion age of 430 Ma for the complex clearly post-dates the major metamorphic event of the Taconic orogeny. The Nd-isotopic data also suggest a relationship between the Cortlandt Complex and a belt of lamprophyric dike rocks to the west, known as the Beemerville trend, which cuts across the metamorphic trends of the Taconic (Ratcliffe 1981). ?? 1982 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1967

Mineral and chemical variations within an ash-flow sheet from Aso caldera, Southwestern Japan

Although products of individual volcanic eruptions, especially voluminous ash-flow eruptions, have been considered among the best available samples of natural magmas, detailed petrographic and chemical study indicates that bulk compositions of unaltered Pleistocene ash-flow tuffs from Aso caldera, Japan, deviate significantly from original magmatic compositions. The last major ash-flow sheet from Aso caldera is as much as 150 meters thick and shows a general vertical compositional change from phenocryst-poor rhyodacite upward into phenocryst-rich trachyandesite; this change apparently reflects in inverse order a compositionally zoned magma chamber in which more silicic magma overlay more mafic magma. Details of these magmatic variations were obscured, however, by: (1) mixing of compositionally distinct batches of magma during upwelling in the vent, as indicated by layering and other heterogeneities within single pumice lumps; (2) mixing of particulate fragments-pumice lumps, ash, and phenocrysts-of varied compositions during emplacement, with the result that separate pumice lenses from a single small outcrop may have a compositional range nearly as great as the bulk-rook variation of the entire sheet; (3) density sorting of phenocrysts and ash during eruption and emplacement, resulting in systematic modal variations with distance from the caldera; (4) addition of xenocrysts, resulting in significant contamination and modification of proportions of crystals in the tuffs; and (5) ground-water leaching of glassy fractions during hydration after cooling. Similar complexities characterize ash-flow tuffs under study in southwestern Nevada and in the San Juan Mountains, Colorado, and probably are widespread in other ash-flow fields as well. Caution and careful planning are required in study of the magmatic chemistry and phenocryst mineralogy of these rocks. ?? 1967 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1969

Experimental introduction of excess Ar40 into a granitic melt

Samples of a Precambrian granite were melted in sealed capsules to produce a radiogenic Ar 40 atmosphere over the melt. The amount of Ar 40 incorporated in the quenched charge was then determined. Under these experimental conditions the amount of argon dissolved in the quenched melt was appreciable and could be an important source of error in potassiumargon dating.

Contributions to Mineralogy and Petrology↗
USGS1977

Stable isotope studies of metasomatic Ca-Fe-Al-Si skarns and associated metamorphic and igneous rocks, Osgood Mountains, Nevada

Garnet-pyroxene skarns were formed 90 m.y. B.P. in the Osgood Mountains at or near contacts of grandiorite with calcareous rocks of the Cambrian Preble Formation. The metasomatic replacement followed contact metamorphic recrystallization of the Preble. The sources, temperature, and variation in H2O/CO2 ratios of the metasomatic fluid are interpreted from 269 analyses of oxygen, carbon, hydrogen, and sulfur isotopes in whole rocks, minerals and inclusion fluids. Skarns formed in three mineralogical stages. Oxygen isotope data indicate that temperatures during the crystallization of garnet, pyroxene and wollastonite (Stage I) were least 550 ?? C, and that the metasomatic fluid had an {Mathematical expression} ??? 0.035 in the massive skarns, and ??? 0.12 in vein skarns up to 3 cm thick. Pore fluids in isotopic equilibrium with garnet in calc-silicate metamorphic rocks, on the other hand, had {Mathematical expression} ??? 0.15. The metasomatic fluids of Stage I were derived primarily from the crystallizing magma. The isotopic composition of magmatic water was ??18O =+9.0, ??D= -30 to -45. Oxygen isotope temperatures of greater than 620 ?? C were determined for the granodiorite. Isotopic and chemical equilibria between mineral surfaces and the metasomatic fluid were approached simultaneously in parts of the skarn several meters or more apart, while isotopic and chemical disequilibria (i.e. zoning) have been preserved between 20 to 40 ??m-thick zones in grandite garnet. More Fe-, or andradite-rich garnet crystallized in more H2O-rich C-O-H fluids ( {Mathematical expression} ??? 0.01) than present with grossularite-rich garnet ( {Mathematical expression}??? 0.035). Stage II was marked by the replacement of garnet and pyroxene by quartz, amphibole, plagioclase, epidote, magnetite, and calcite. Many of the replacement reactions took place over a relatively narrow range in temperature (480-550 ?? C), as indicated by 18O fractionations between quartz and amphibole. Meteoric water comprised 20 to 50% of the metasomatic fluid during Stage II. Calcite was formed along with pyrite, minor pyrrhotite, and chalcopyrite during Stage III, although the crystallization of pyrite and calcite had begun earlier, during Stages I and II, respectively. Carbon and sulfur isotope compositions of calcite and pyrite indicate a magmatic source for most of the C and S in the metasomatic fluids of Stage III. By the end of Stage III, meteoric water constituted as much as 100% of the metasomatic fluid. Minerals from grandiorite and skarn do not show large depletions in 18O because the oxygen isotope composition of the metasomatic fluid was buffered by the calcareous wall rocks and the grandiorite. Meteoric water in the vicinity of the Osgood Mountains during the Late Crectaceous (??18Ocale. ??? -14.0, ??D = - 107) was slightly enriched in 18O and D relative to present-day meteoric water (??18O = 15.9, ??D = - 117) ?? 1977 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1979

U-Th-Pb geochronology of the Massabesic Gneiss and the granite near Milford, South-Central New Hampshire: New evidence for avalonian basement and taconic and alleghenian disturbances in Eastern New England

U-Th-Pb systematics for zircon and monazite from Massabesic Gneiss (paragneiss and orthogneiss) and the granite near Milford, New Hampshire, were determined. Zircon morphology suggests that the paragneiss may be volcaniclastic (igneous) in origin, and thus the age data probably record the date (minimum of 646 m.y.) at which the rock was extruded. A two-stage lead-loss model is proposed to explain the present array of data points on a concordia diagram. Orthogneiss ages range only narrowly and are clustered around 475 m.y. Data for the granite of Milford, New Hampshire, are scattered, but may be interpreted in terms of inheritance and modern lead loss, yielding a crystallization age of 275 m.y. This is the only known occurrence of Avalonian-type basement in New Hampshire and as such provides evidence for the location of the paleo-Africa-paleo- North America suture. The geochronology also further documents the occurrence of disturbances during the Ordovician and Permian. ?? 1979 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1980

Nd-isotopes in selected mantle-derived rocks and minerals and their implications for mantle evolution

The Sm-Nd systematics in a variety of mantle-derived samples including kimberlites, alnoite, carbonatite, pyroxene and amphibole inclusions in alkali basalts and xenolithic eclogites, granulites and a pyroxene megacryst in kimberlites are reported. The additional data on kimberlites strengthen our earlier conclusion that kimberlites are derived from a relatively undifferentiated chondritic mantle source. This conclusion is based on the observation that the e{open}Nd values of most of the kimberlites are near zero. In contrast with the kimberlites, their garnet lherzolite inclusions show both time-averaged Nd enrichment and depletion with respect to Sm. Separated clinopyroxenes in eclogite xenoliths from the Roberts Victor kimberlite pipe show both positive and negative e{open}Nd values suggesting different genetic history. A whole rock lower crustal scapolite granulite xenolith from the Matsoku kimberlite pipe shows a negative e{open}Nd value of -4.2, possibly representative of the base of the crust in Lesotho. It appears that all inclusions, mafic and ultramafic, in kimberlites are unrelated to their kimberlite host. The above data and additional Sm-Nd data on xenoliths in alkali basalts, alpine peridotite and alnoite-carbonatites are used to construct a model for the upper 200 km of the earth's mantle - both oceanic and continental. The essential feature of this model is the increasing degree of fertility of the mantle with depth. The kimberlite's source at depths below 200 km in the subcontinental mantle is the most primitive in this model, and this primitive layer is also extended to the suboceanic mantle. However, it is clear from the Nd-isotopic data in the xenoliths of the continental kimberlites that above 200 km the continental mantle is distinctly different from their suboceanic counterpart. ?? 1980 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1988

Geochemistry and origin of albite gneisses, northeastern Adirondack Mountains, New York

Albite gneisses containing up to 8.7 percent Na2O and as little as 0.1% K2O comprise a significant part of the Proterozoic Lyon Mountain Gneiss in the Ausable Forks Quadrangle of the northeastern Adirondacks, New York State. Two distinct types of albite gneisses are present. One is a trondhjemitic leucogneiss (LAG) consisting principally of albite (Ab95-Ab98) and quartz with minor magnetite and, locally, minor amounts of amphibole or acmiterich pyroxene. LAG probably originated by metamorphism of a rhyolitie or rhyodacitic ash-flow tuff with A-type geochemical affinities, following post-depositional analcitization in a saline or saline-alkaline environment. The other type is a mafic albite gneiss (MAG) containing albite and pyroxene along with 0-45 percent quartz, minor amphibole, and titanite. MAG locally displays pinstripe banding and contains albite (Ab98) megacrysts up to 5 cm across. Its precursor may have been a sediment composed of diagenetic analcite or albite, dolomite, and quartz. Both types of albite gneiss are interlayered with granitic gneisses (LMG) of variable composition derived from less altered tuffs. A potassium-rich (up to 9.7% K2O) microcline gneiss facies may have had a protolith rich in diagenetic K feldspar. We propose that the albite gneisses and associated granitic gneisses are the granulite-facies metamorphic equivalent of a bimodal, dominantly felsic, volcanic suite with minor intercalated sediments, probably including evaporites. The volcanics were erupted in an anorogenic setting, such as an incipient or failed intracontinental rift. Deposition took place in a closed-basin, playa lake environment, where diagenetic alteration resulted in redistribution of the alkalis and strong oxidation. ?? 1988 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1988

Contrasting serpentinization processes in the eastern Central Alps

Stable isotope compositions have been determined for serpentinites from between Davos (Arosa-Platta nappe, Switzerland) and the Valmalenco (Italy). ??D and ??18O values (-120 to -60 and 6-10???, respectively) in the Arosa-Platta nappe indicate that serpentinization took place on the continent at relatively low temperatures in the presence of limited amounts of metamorphic fluids that contained a component of meteoric water. One sample of chrysotile has a ??18O value of 13??? providing evidence of high W/R ratios and low formation temperature of lizardite-chrysotile in this area. In contrast, relatively high ??D values (-42 to -34???) and low ??18O values (4.4-7.4???) for serpentine in the eastern part of the Valmalenco suggest a serpentinization process that took place at moderate temperatures in fluids that were dominated by ocean water. The antigorite in the Valmalenco is the first reported example of continental antigorite with an ocean water signature. An amphibole sample from a metasomatically overprinted contact zone to metasediments (??D=-36???) indicates that the metasomatic event also took place in the presence of ocean water. Lower ??D values (-93 to -60???) of serpentines in the western part of the Valmalenco suggest a different alteration history possibly influenced by fluids associated with contact metamorphism. Low water/rock ratios during regional metamorphism (and metasomatism) have to be assumed for both regions. ?? 1988 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1970

The strontium isotopic composition of basalts from the Gordo and Juan de Fuca Rises, northeastern Pacific Ocean

The strontium isotopic compositions have been determined for twelve tholeiitic basalts dredged from the Gordo and Juan de Fuca Rises. Sr 87 /Sr 86 ratios range from 0.7012 to 0.7031 and average 0.7026. These data, combined with other data from the East Pacific Rise indicate that tholeiite basalts being erupted along the active rises, in the Pacific Ocean, contain less radiogenic Sr 87 than basalts erupted on the islands. These isotopic differences between the ocean-ridge tholeiite and the more alkali island basalts indicate that variations in Rb/Sr have persisted in the mantle for billions of years. The possible origins and distribution of these heterogeneties are discussed.

Contributions to Mineralogy and Petrology↗
USGS1970

Lead and strontium isotopes in rocks of the Absaroka volcanic field, Wyoming

The Absaroka volcanic field is comprised of predominant andesitic volcaniclastic rocks and less abundant potassium-rich mafic lavas (shoshonites and absarokites). Strontium and lead isotopic variations preclude a simple derivation from an isotopically uniform source: Sr 87 /Sr 86 , 0.7042 to 0.7090; Pb 206 /Pb 204 , 16.31 to 17.30; Pb 208 /Pb 204 , 36.82 to 37.64. We postulate that these rocks were derived from a lower crust or upper mantle which underwent a preferential loss of uranium relative to lead approximately 2800±200 m.y. ago. Variations in lead and strontium isotopic compositions are thought to reflect small inhomogeneities in U/Pb and Rb/Sr ratios in the source.

Wyoming↗
USGS1982

Genetic relations among basic lavas and ultramafic nodules: Evidence from oxygen isotope compositions

??18O values of unaltered basic lavas range from 4.9 to 8.3 but different types of basalts are usually restricted to narrow and distinct ranges of isotopic composition. The average ??18O values for Hawaiian tholeiites, mid-ocean ridge tholeiites, and alkali basalts are 5.4, 5.7, and 6.2 permil, respectively. Potassic lavas and andesites tend to be more 18O rich with ??18O values between 6.0 and 8.0 permil. The differences among the oxygen isotopic compositions of most of these lavas can be attributed to partial melting of isotopically distinct sources. The oxygen isotope compositions of the sources may be a function of prior melting events which produce 18O-depleted partial melts and 18O-enriched residues as a consequence of relatively large isotopic fractionations that exist at high temperatures. It is proposed that lavas with relatively low ??18O values are derived from primitive, 18O-depleted sources whereas 18O-rich basalts are produced from refractory sources that have already produced partial melts. High temperature fractionations among silicate liquids and coexisting minerals can be used in conjunction with the oxygen isotope compositions of ultramafic nodules to place constraints on the genetic relations between some nodules and different types of basic lavas. ?? 1982 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1971

Isotopic composition of strontium in three basalt-andesite centers along the Lesser Antilles arc

Si 87 /Sr 86 ratios have been determined for lavas and py lastic rocks from three basalt-andesite centers along the Lesser Antilles arc—Mt. Misery on the island of St. Kitts, Soufriere on the island of St. Vincent, and Carriacou, an island of The Grenadines. The average Si 87 /Sr 86 content of these rocks is 0.7038 for Mt. Misery, 0.7041 for Soufriere, and 0.7053 for Carriacou. All the Sr 87 /Sr 86 values from each center are the same within analytical uncertainty (±0.0002). The constancy of strontium isotopic data within each center supports the hypothesis that basalts and andesites for each specific center investigated are generated from the same source — in agreement with petrographic and major- and minor-element data. Strontium isotopic compositions and elemental concentrations, particularly of strontium and nickel, indicate that this source was mantle peridotite and that the relationship between the respective basalts and andesites is probably fractional crystallization.

Contributions to Mineralogy and Petrology↗
USGS1971

Distribution of elements in biotite-hornblende pairs and in an orthopyroxene-clinopyroxene pair from zoned plutons, northern Sierra Nevada, California

Distribution of major and minor elements has been determined for five hornblende-biotite pairs from hornblende-biotite quartz diorite and monzotonalite and for a clinopyroxene-orthopyroxene pair from pyroxene diorite collected from the border zones and centers of zoned plutons in the northern Sierra Nevada, California. The distribution coefficients K d [Mg/Fe] for biotite/hornblende are of the same magnitude (0.61–0.67) for both the mafic border zone and the silicic center. For comparison, K D [Mg/Fe] values for biotite/hornblende from plutonic rocks of the central Sierra Nevada and the southern California batholith were calculated from data published by others. Rocks of the oldest age group (ca. 150 m.y.) in the central Sierra Nevada have an average distribution coefficient, K D , of 0.64, close to the average K D in the study area, where K-Ar dates are 143 to 129 m.y. The intermediate age group has an average K D =0.81, and the youngest group has K D =0.77. K D [Mg/Fe] for biotite/hornblende from the southern California batholith is 0.83, close to the average of the intermediate age group in the central Sierra Nevada. The calculated difference in pressure of crystallization between rocks of the Feather River area and the southern California batholith is 1 kb; the rocks of the Feather River area being crystallized at a higher pressure. This is in good agreement with the low-pressure contact metamorphism in the south (pyroxene hornfels facies), as compared with a medium-pressure metamorphism around the northern plutons, where andalusitesillimanite-cordierite and andalusite-staurolite subfacies of the amphibolite facies indicate pressures of about 4 kb. Trace elements Cr, V, Ni, Co, Ga are distributed equally between biotite and hornblende, whereas Ba and possibly Cu are concentrated in biotite and Sr and Sc and possibly Zr in hornblende.

California↗
USGS1977

The origin of garnet in the anorthosite-charnockite suite of the Adirondacks

Detailed analysis of textural and chemical criteria in rocks of the anorthosite-charnockite suite of the Adirondack Highlands suggests that development of garnet in silica-saturated rocks of the suite occurs according to the reaction: {Mathematical expression}, where ?? is a function of the distribution of Fe and Mg between the several coexisting ferromagnesian phases. Depending upon the relative amounts of Fe and Mg present, quartz may be either a reactant or a product. Using an aluminum-fixed reference frame, this reaction can be restated in terms of a set of balanced partial reactions describing the processes occurring in spatially separated domains within the rock. The fact that garnet invariably replaces plagioclase as opposed to the other reactant phases indicates that the aluminum-fixed model is valid as a first approximation. This reaction is univariant and produces unzoned garnet. It differs from a similar equation proposed by de Waard (1965) for the origin of garnet in Adirondack metabasic rocks, i.e. 6 Orthopyroxene+2 Anorthite = Clinopyroxene+Garnet+2 Quartz, the principle difference being that iron oxides (ilmenite and/or magnetite) are essential reactant phases in the present reactions. The product assemblage (garnet+clinopyroxene+plagioclase ?? orthopyroxene ?? quartz) is characteristic of the clinopyroxene-almandine subfacies of the granulite facies. ?? 1977 Springer-Verlag.

Contributions to Mineralogy and Petrology↗