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At least 109 records · Page 6Linked to original sources
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↗
USGS1988

Crustal contributions to arc magmatism in the Andes of Central Chile

Fifteen andesite-dacite stratovolcanoes on the volcanic front of a single segment of the Andean arc show along-arc changes in isotopic and elemental ratios that demonstrate large crustal contributions to magma genesis. All 15 centers lie 90 km above the Benioff zone and 280??20 km from the trench axis. Rate and geometry of subduction and composition and age of subducted sediments and seafloor are nearly constant along the segment. Nonetheless, from S to N along the volcanic front (at 57.5% SiO2) K2O rises from 1.1 to 2.4 wt %, Ba from 300 to 600 ppm, and Ce from 25 to 50 ppm, whereas FeO*/MgO declines from >2.5 to 1.4. Ce/Yb and Hf/Lu triple northward, in part reflecting suppression of HREE enrichment by deep-crustal garnet. Rb, Cs, Th, and U contents all rise markedly from S to N, but Rb/Cs values double northward - opposite to prediction were the regional alkali enrichment controlled by sediment subduction. K/Rb drops steeply and scatters greatly within many (biotite-free) andesitic suites. Wide diversity in Zr/Hf, Zr/Rb, Ba/Ta, and Ba/La within and among neighboring suites (which lack zircon and alkali feldspar) largely reflects local variability of intracrustal (not slab or mantle) contributions. Pb-isotope data define a limited range that straddles the Stacey-Kramers line, is bracketed by values of local basement rocks, in part plots above the field of Nazca plate sediment, and shows no indication of a steep (mantle+sedimentary) Pb mixing trend. 87Sr/86Sr values rise northward from 0.7036 to 0.7057, and 143Nd/144Nd values drop from 0.5129 to 0.5125. A northward climb in basal elevation of volcanic-front edifices from 1350 m to 4500 m elevation coincides with a Bougueranomaly gradient from -95 to -295 mgal, interpreted to indicate thickening of the crust from 30-35 km to 50-60 km. Complementary to the thickening crust, the mantle wedge beneath the front thins northward from about 60 km to 30-40 km (as slab depth is constant). The thick northern crust contains an abundance of Paleozoic and Triassic rocks, whereas the proportion of younger arc-intrusive basement increases southward. Primitive basalts are unknown anywhere along the arc. Base-level isotopic and chemical values for each volcano are established by blending of subcrustal and deep-crustal magmas in zones of melting, assimilation, storage and homogenization (MASH) at the mantle-crust transition. Scavenging of mid-to upper-crustal silicic-alkalic melts and intracrustal AFC (prominent at the largest center) can subsequently modify ascending magmas, but the base-level geochemical signature at each center reflects the depth of its MASH zone and the age, composition, and proportional contribution of the lowermost crust. ?? 1988 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1983

The granite problem as exposed in the southern Snake Range, Nevada

A geochemically and mineralogically diverse group of granitoids is present within an area of 900 km2 in the southern Snake Range of eastern Nevada. The granitoids exposed range in age from Jurassic through Cretaceous to Oligocene and include two calcic intrusions, two different types of two-mica granites, and aplites. The younger intrusions appear to have been emplaced at progressively more shallow depths. All of these granitoid types are represented elsewhere in the eastern Great Basin, but the southern Snake Range is distinguished by the grouping of all these types within a relatively small area. The Jurassic calcic pluton of the Snake Creek-Williams Canyon area displays large and systematic chemical and mineralogical zonation over a horizontal distance of five km. Although major element variations in the pluton compare closely with Daly's average andesite-dacite-rhyolite over an SiO2 range of 63 to 76 percent, trace element (Rb, Sr, Ba) variations show that the zonation is the result of in situ fractional crystallization, with the formation of relatively mafic cumulates on at least one wall of the magma chamber. Models of trace element and isotopic data indicate that relatively little assimilation took place at the level of crystallization. Nonetheless, an initial 87Sr/86Sr value of 0.7071 and ??18O values of 10.2 to 12.2 permil suggest a lower crustal magma that was contaminated by upper crustal clastic sedimentary rocks before crystallization. The involvement of mantle-derived magmas in its genesis is difficult to rule out. Two other Jurassic plutons show isotopic and chemical similarities to the Snake Creek-Williams Canyon pluton. Cretaceous granites from eastern Nevada that contain phenocrystic muscovite are strongly peraluminous, and have high initial Sr-isotope ratios and other features characteristic of S-type granitoids. They were probably derived from Proterozoic metasediments and granite gneisses that comprise the middle crust of this region. Another group of granitoids (including the Tertiary aplites) show chemical, mineralogic, and isotopic characteristics intermediate between the first two groups and may have been derived by contamination of magmas from the lower crust by the midcrustal metasediments. ?? 1983 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1970

Distribution of rubidium between sodic sanidine and natural silicic liquid

Phenocrysts of sodic sanidine from twelve upper Cenozoic units of silicic ash-flow tuff and lava from the Western United States contain from 0.25 to 0.45 the Rb present in the associated groundmass materials. The ratios of potassium to rubidium in the sanidines are, on the average, about four times greater than those of the groundmass. Separation of phenocrystic sanidine from salic melts provides an efficient method for raising the Rb content and lowering the K/Rb ratio of the melts, although the amount of differentiation probably is limited by continuous reequilibration of the alkalis between crystal and liquid phases through ion exchange. Syenites of cumulate origin will have appreciably lower Rb contents and higher K/Rb ratios than the melts from which they precipitated. Available data on the distribution of Rb between synthetic biotite and K-sanidine demonstrate that the separation of biotite probably will not deplete salic melts in Rb relative to K.

Contributions to Mineralogy and Petrology↗
USGS1988

Origin of ultramafic xenoliths containing exsolved pyroxenes from Hualalai Volcano, Hawaii

Hualalai Volcano, Hawaii, is best known for the abundant and varied xenoliths included in the historic 1800 Kaupulehu alkalic basalt flow. Xenoliths, which range in composition from dunite to anorthosite, are concentrated at 915-m elevation in the flow. Rare cumulate ultramafic xenoliths, which include websterite, olivine websterite, wehrlite, and clinopyroxenite, display complex pyroxene exsolution textures that indicate slow cooling. Websterite, olivine websterite, and one wehrlite are spinel-bearing orthopyroxene +olivine cumulates with intercumulus clinopyroxene +plagioclase. Two wehrlite samples and clinopyroxenite are spinel-bearing olivine cumulates with intercumulus clinopyroxene+orthopyroxene + plagioclase. Two-pyroxene geothermometry calculations, based on reconstructed pyroxene compositions, indicate that crystallization temperatures range from 1225° to 1350° C. Migration or unmixing of clinopyroxene and orthopyroxene stopped between 1045° and 1090° C. Comparisons of the abundance of K 2 O in plagioclase and the abundances of TiO 2 and Fe 2 O 3 in spinel of xenoliths and mid-ocean ridge basalt, and a single 87 Sr/ 86 Sr determination, indicate that these Hualalai xenoliths are unrelated to mid-ocean ridge basalt. Similarity between the crystallization sequence of these xenoliths and the experimental crystallization sequence of a Hawaiian olivine tholeiite suggest that the parental magma of the xenoliths is Hualalai tholeiitic basalt. Xenoliths probably crystallized between about 4.5 and 9 kb. The 155°–230° C of cooling which took place over about 120 ka — the age of the youngest Hualalai tholeiitic basalt — yield maximum cooling rates of 1.3×10 −3 –1.91×10 −3 °C/yr. Hualalai ultramafic xenoliths with exsolved pyroxenes crystallized from Hualalai tholeiitic basalt and accumulated in a magma reservoir located between 13 and 28 km below sealevel. We suspect that this reservoir occurs just below the base of the oceanic crust at about 19 km below sealevelz

Hawaii↗
USGS1988

Garnet compositions and their use as indicators of peraluminous granitoid petrogenesis - southeastern Arabian Shield

Garnet, an uncommon accessory mineral in igneous rocks, occurs in seven small peraluminous granitoid plutons in the southeastern Arabian Shield; textural equilibrium between garnet and other host granitoid minerals indicates that the garnets crystallized from their host magmas. Compositions of the garnets form three groups that reflect host-granitoid compositions, which in turn reflect source compositions and tectonic regimes in which the host magmas were generated. Garnets from the seven plutons have almandine-rich cores and spessartine-rich rims. This reverse zoning depicts host magma compositional evolution; i.e. rimward spessartine enrichment resulted from progressive, host-magma manganese enrichment. The garnets are heavy rare-earth element enriched; (Lu/La)N ranges from 13 to 355 and one of the garnets contains spectacularly elevated abundances of Y, Ta, Th, U, Zn, Zr, Hf, Sn, and Nb. Involvement of garnets with these trace element characteristics in magma genesis or evolution can have dramatic effects on trace element signatures of the resulting magmas. Other researchers suggest that Mn-enriched magmas are most conducive to garnet nucleation. Although the garnetiferous granitoids discussed here are slightly Mn enriched, other genetically similar peraluminous Arabian granitoids lack garnet; Mn enrichment alone does not guarantee garnet nucleation. The presence of excess alumina in the magma may be a prerequisite for garnet nucleation. ?? 1988 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1984

Geochronology of Precambrian granites and associated U-Ti-Th mineralization, northern Olary province, South Australia

Proterozoic granitoids and metamorphic rocks in the Olary province of the Willyama block of South Australia host ore-grade amounts of U-Th-Ti and U-Fe-Ti-Th minerals. U-Pb-Th isotope analyses on zircons from all granitoids associated with the Crocker Well brannerite deposit indicate that these granitoids were intruded within a short time span, close to the 1579.2??1.5 m.y. age of the brannerite-bearing host-rock. Though the early Paleozoic Delamerian orogeny was intense in this region, the zircon isotopic systems remained unaffected; rather, the best-defined zircon chords on concordia plots show a welldefined lower intercept of 43.8??6.5 Ma, which can only be associated with early Tertiary block faulting. Pb-U-Th isotope analyses on brannerite from the Crocker Well deposit and davidite from the Mt. Victoria deposit and the Radium Hill deposit yield badly scattered and discordant apparent ages that suggest a primary age at least as old as the age of the Crocker Well granitoids, followed by a severe disturbance in the early Paleozoic. ?? 1984 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1981

Stable isotope systematics in mesozoic granites of Central and Northern California and Southwestern Oregon

18O, D, and H2O+ contents were measured for whole-rock specimens of granitoid rocks from 131 localitics in California and southwestern Oregon. With 41 new determinations in the Klamath Mountains and Sierra Nevada, initial strontium isotope ratios are known for 104 of these samples. Large variations in ??18O (5.5 to 12.4), ??D (-130 to -31), water contents (0.14 to 2.23 weight percent) and initial strontium isotope ratios (0.7028 to 0.7095) suggest a variety of source materials and identify rocks modified by secondary processes. Regular patterns of variation in each isotopic ratio exist over large geographical regions, but correlations between the ratios are generally absent except in restricted areas. For example, the regular decrease in ??D values from west to east in the Sierra Nevada batholith is not correlative with a quite complex pattern of ??18O values, implying that different processes were responsible for the isotopic variations in these two elements. In marked contrast to a good correlation between (87Sr/86Sr)o and ??18O observed in the Peninsular Ranges batholith to the south, such correlations are lacking except in a few areas. ??D values, on the other hand, correlate well with rock types, chemistry, and (87Sr/86Sr)o except in the Coast Ranges where few of the isotopic signatures are primary. The uniformly low ??D values of samples from the Mojave Desert indicate that meteoric water contributed much of the hydrogen to the rocks in that area. Even so, the ??18O values and 18O fractionations between quartz and feldspar are normal in these same rocks. This reconnaissance study has identified regularities in geochemical parameters over enormous geographical regions. These patterns are not well understood but merit more detailed examination because they contain information critical to our understanding of the development of granitoid batholiths. ?? 1981 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1984

Contrasting fluid/rock interaction between the Notch Peak granitic intrusion and argillites and limestones in western Utah: evidence from stable isotopes and phase assemblages

The Jurassic Notch Peak granitic stock, western Utah, discordantly intrudes Cambrian interbedded pure limestones and calcareous argillites. Contact metamorphosed argillite and limestone samples, collected along traverses away from the intrusion, were analyzed for ??18O, ??13C, and ??D. The ??13C and ??18O values for the limestones remain constant at about 0.5 (PDB) and 20 (SMOW), respectively, with increasing metamorphic grade. The whole rock ??18O values of the argillites systematically decrease from 19 to as low as 8.1, and the ??13C values of the carbonate fraction from 0.5 to -11.8. The change in ??13C values can be explained by Rayleigh decarbonation during calcsilicate reactions, where calculated {Mathematical expression} is about 4.5 permil for the high-grade samples and less for medium and low-grade samples suggesting a range in temperatures at which most decarbonation occurred. However, the amount of CO2 released was not anough to decrease the whole rock ??18O to the values observed in the argillites. The low ??18O values close to the intrusion suggest interaction with magmatic water that had a ??18O value of 8.5. The extreme lowering of ??13C by fractional devolatilization and the lowering of ??18O in argillites close to the intrusion indicates oxgen-equivalent fluid/rock ratios in excess of 1.0 and X(CO2)F of the fluid less than 0.2. Mineral assemblages in conjunction with the isotopic data indicate a strong influence of water infiltration on the reaction relations in the argillites and separate fluid and thermal fronts moving thru the argillites. The different stable isotope relations in limestones and argillites attest to the importance of decarbonation in the enhancement of permeability. The flow of fluids was confined to the argillite beds (argillite aquifers) whereas the limestones prevented vertical fluid flow and convective cooling of the stock. ?? 1984 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1981

Subcalcic diopsides from kimberlites: Chemistry, exsolution microstructures, and thermal history

Twenty-six subcalcic diopside megacrysts (Ca/(Ca+ Mg)) = 0.280-0.349, containing approximately 10 mol% jadeite, from 15 kimberlite bodies in South Africa, Botswana, Tanzania, and Lesotho, have been characterized by electron microprobe analysis, X-ray-precession photography, and transmission electron microscopy. Significant exsolution of pigeonite was observed only in those samples for which Ca/(Ca+Mg)???0.320. The exsolution microstructure consists of coherent (001) lamellae with wavelengths ranging from 20 to 31 nm and compositional differences between the hosts and lamellae ranging from 10 to 30 mol% wollastonite. These observations suggest that the exsolution reaction mechanism was spinodal decomposition and that the megacrysts have been quenched at various stages of completion of the decomposition process. Annealing experiments in evacuated SiO2 glass tubes at 1,150?? C for 128 hours failed to homogenize microstructure, whereas, at 5 kbar and 1,150?? C for only 7.25 hours, the two lattices were homogenized. This "pressure effect" suggests that spinodal decomposition in the kimberlitic subcalcic diopside megacrysts can only occur at depths less than ???15 km; the cause of the effect may be the jadeite component in the pyroxene. "Apparent quench" temperatures for the exsolution process in the megacrysts range from 1,250?? C to 990?? C, suggesting that decomposition must have commenced at temperatures of more than ???1,000?? C. These P-T limits lead to the conclusion that, in those kimberlites where spinodal decomposition has occurred in subcalcic diopside megacrysts, such decomposition occurred at shallow levels (<15 km) and, at the present erosion level, temperatures must have been greater than 1,000?? C. ?? 1981 Springer-Verlag.

Contributions to Mineralogy and Petrology↗