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At least 883 records · Page 49Linked to original sources
USGS1974

Presentation and interpretation of chemical data for igneous rocks

Arguments are made in favor of using variation diagrams to plot analyses of igneous rocks and their derivatives and modeling differentiation processes by least-squares mixing procedures. These methods permit study of magmatic differentiation and related processes in terms of all of the chemical data available. Data are presented as they are reported by the chemist and specific processes may be modeled and either quantitatively described or rejected as inappropriate or too simple. Examples are given of the differing interpretations that can arise when data are plotted on an AEM ternary vs. the same data on a full set of MgO variation diagrams. Mixing procedures are illustrated with reference to basaltic lavas from the Columbia Plateau.

Idaho, Washington, Oregon↗
USGS1974

Chemistry and mineralogy of garnet pyroxenites from Sabah, Malaysia

Garnet pyroxenites and corundum-garnet amphibolites from the Dent peninsula of eastern Sabah (North Borneo) occur as blocks in a slump breccia deposit of late Miocene age. The earliest formed minerals include pyrope-almandine garnet, tschermakitic augite, pargasite, and rutile. Cumulate textures are present in two of the six specimens studied. The earlier fabric has been extensively brecciated and partly replaced by plagioclase, ilmenite, and a fibrous amphibole. The bulk composition and mineralogy of these rocks are similar to those of garnet pyroxenite lenses within ultramafic rocks. Estimated temperature and pressure for the origin of the Sabah garnet pyroxenites is 850±150° C and 19±4 kbar.

Contributions to Mineralogy and Petrology↗
USGS1989

Boron isotopic composition of tourmaline from massive sulfide deposits and tourmalinites

Boron isotope ratios (11B/10B) have been measured on 60 tourmaline separates from over 40 massive sulfide deposits and tourmalinites from a variety of geologic and tectonic settings. The coverage of these localities is global (5 continents) and includes the giant ore bodies at Kidd Creek and Sullivan (Canada), Broken Hill (Australia), and Ducktown (USA). Overall, the tourmalines display a wide range in ??11B values from -22.8 to +18.3??? Possible controls over the boron isotopic composition of the tourmalines include: 1) composition of the boron source, 2) regional metamorphism, 3) water/rock ratios, 4) seawater entrainment, 5) temperature of formation, and 6) secular variations in seawater ??11B. The most significant control appears to be the composition of the boron source, particularly the nature of footwall lithologies; variations in water/ rock ratios and seawater entrainment are of secondary importance. The boron isotope values seem especially sensitive to the presence of evaporites (marine and non-marine) and carbonates in source rocks to the massive sulfide deposits and tourmalinites. ?? 1989 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1994

Petrogenesis of the highly potassic 1.42 Ga Barrel Spring pluton, southeastern California, with implications for mid-Proterozoic magma genesis in the southwestern USA

Syenites from the Barrel Spring pluton were emplaced in the Early Proterozoic Mojave crustal provine of southeastern California at 1.42 Ga. All rocks, even the most mafic, are highly enriched in incompatible elements (e.g. K 2 O 4–12 wt%, Rb 170–370 ppm, Th 12–120 ppm, La 350–1500xchondrite, La/Yb n 35–100). Elemental compositions require an incompatible element-rich but mafic (or ultramafic) source. Trace element models establish two plausible sources for Barrel Spring magmas: (1) LREE enriched garnet websterite with accessory apatite±rutile (enriched lithospheric mantle), and (2) garnet amphibolite or garnet-hornblende granulite with enriched alkali basalt composition, also with accessory apatite±rutile (mafic lower crust). Nd and Pb isotopic ratios do not distinguish a crust vs mantle source, but eliminate local Mojave province crust as the principal one, and indicate that generation of the enriched source occurred several hundred million years before emplacement of the Barrel Spring pluton. 1.40–1.44 Ga potassic granites are common in southeastern California, suggesting a genetic link between the Barrel Spring pluton and the granites; however, although the same thermal regime was probably responsible for producing both the granitic and syentic magmas, elemental and isotopic compositions preclude a close relationship. Isotopic similarity of the Barrel Spring pluton to 1.40–1.44 Ga granites emplaced in the Central Arizona crustal province to the east may imply that a common component was present in the lithosphere of these generally distinct regions.

California↗
USGS1980

A lead isotope study of mineralization in the Saudi Arabian Shield

New lead isotope data are presented for some late Precambrian and early Paleozoic vein and massive sulfide deposits in the Arabian Shield. Using the Stacey Kramers (1975) model for lead isotope evolution, isochron model ages range between 720 m.y. and 420 m.y. Most of the massive sulfide deposits in the region formed before 680 m.y. ago, during evolution of the shield. Vein type mineralization of higher lead content occurred during the Pan African event about 550 m.y. ago and continued through the Najd period of extensive faulting in the shield that ended about 530 m.y. ago. Late post-tectonic metamorphism may have been responsible for vein deposits that have model ages less than 500 m.y. Alternatively some of these younger model ages may be too low due to the mineralizing fluids acquiring radiogenic lead from appreciably older local crustal rocks at the time of ore formation. The low207Pb/204Pb ratios found for the deposits in the main part of the shield and for those in north-eastern Egypt, indicate that the Arabian craton was formed in an oceanic crustal environment during the late Precambrian. Involvement of older, upper-crustal material in the formation of the ore deposits in this part of the shield is precluded by their low207Pb/204Pb and208Pb/204Pb characteristics. In the eastern part of the shield, east of longitude 44??20???E towards the Al Amar-Idsas fault region, lead data are quite different. They exhibit a linear207Pb/204Pb-206Pb/204Pb relationship together with distinctly higher208Pb/204Pb characteristics. These data imply the existence of lower crustal rocks of early Proterozoic age that apparently have underthrust the shield rocks from the east. If most of the samples we have analyzed from this easterly region were mineralized 530 m.y. ago, then the age of the older continental rocks is 2,100??300 m.y. (2??). The presence of upper crustal rocks, possibly also of early Proterozoic age, is indicated by galena data from Hailan in South Yemen and also from near Muscat in Oman. These data are the first to indicate such old continental material in these regions. ?? 1980 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1982

Genetic implications of minor-element and Sr-isotope geochemistry of alkaline rock complexes in the Wet Mountains area, Fremont and Custer counties, Colorado

Concentrations of Rb, Sr, and REE (rare earth elements), and Sr-isotopic ratios in rocks of the Cambrian alkaline complexes in the Wet Mountains area, Colorado, show that rocks formed as end-products of a variety of magmas generated from different source materials. The complexes generally contain a bimodal suite of cumulus mafic-ultramafic rocks and younger leucocratic rocks that include nepheline syenite and hornblende-biotite syenite in the McClure Mountain Complex, nepheline syenite pegmatite in the Gem Park Complex, and quartz syenite in the complex at Democrat Creek. The nepheline syenite and hornblende-biotite syenite at McClure Mountain (535??5m.y.) are older than the syenitic rocks at Democrat Creek (511??8m.y.). REE concentrations indicate that the nepheline syenite at McClure Mountain cannot be derived from the hornblende-biotite syenite, which it intrudes, or from the associated mafic-ultramafic rocks. REE also indicate that mafic-ultramafic rocks at McClure Mountain have a source distinct from that of the mafic-ultramafic rocks at Democrat Creek. In the McClure Mountain Complex, initial87Sr/86Sr ratios for mafic-ultramafic rocks (0.7046??0.0002) are similar to those of hornblende-biotite syenite (0.7045??0.0002), suggesting a similar magmatic source, whereas ratios for carbonatites (0.7038??0.0002) are similar to those of nepheline syenite (0.7038??0.0002). At Democrat Creek, initial ratios of syenitic rocks (0.7032??0.0002) and mafic-ultramafic rocks (0.7028??0.0002) are different from those of corresponding rocks at McClure Mountain. ?? 1982 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1983

Distribution of oceanic and continental leads in the Arabian-Nubian Shield

New common lead data for feldspar, whole-rock, and galena samples from the Arabian-Nubian Shield, together with data from previous work, can be divided into two main groups. Group I leads have oceanic (mantle) characteristics, whereas group II leads have incorporated a continental-crustal component of at least early Proterozoic age. The group I leads are found in rocks from the Red Sea Hills of Egypt and the western and southern parts of the Arabian Shield. Group II leads are found in rocks from the northeastern and eastern parts of the Arabian Shield, as well as from the southeastern Shield near Najran. They are also found in rocks to the south in Yemen, to the east in Oman, and to the west at Aswan, Egypt. This distribution of data suggests that the Arabian-Nubian Shield has an oceanic core flanked by rocks that have developed, at least in part, from older continental material. Two mechanisms are suggested by which this older lead component could have been incorporated into the late Proterozoic rocks, and each may have operated in different parts of the Shield. The older lead component either was derived directly from an underlying early Proterozoic basement or was incorporated from subducted pelagic sediments or sediments derived from an adjacent continent. New U-Pb zircon data indicate the presence of an early Proterozoic basement southeast of Jabal Dahul in the eastern Arabian Shield. These data, together with 2,000-Ma-old zircons from the Al Amar fault zone, verify the implication of the common lead data that at least a part of the eastern Arabian Shield has an older continental basement. Because continental margins are particularly favorable locations for development of ore deposits, these findings may have important economic implications, particularly for tin, tungsten, and molybdenum exploration. ?? 1983 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1984

Magmatic inclusions in rhyolites, contaminated basalts, and compositional zonation beneath the Coso volcanic field, California

Basaltic lava flows and high-silica rhyolite domes form the Pleistocene part of the Coso volcanic field in southeastern California. The distribution of vents maps the areal zonation inferred for the upper parts of the Coso magmatic system. Subalkalic basalts (<50% SiO 2 ) were erupted well away from the rhyolite field at any given time. Compositional variation among these basalts can be ascribed to crystal fractionation. Erupted volumes of these basalts decrease with increasing differentiation. Mafic lavas containing up to 58% SiO 2 , erupted adjacent to the rhyolite field, formed by mixing of basaltic and silicic magma. Basaltic magma interacted with crustal rocks to form other SiO 2 -rich mafic lavas erupted near the Sierra Nevada fault zone. Several rhyolite domes in the Coso volcanic field contain sparse andesitic inclusions (55–61% SiO 2 ). Pillow-like forms, intricate commingling and local diffusive mixing of andesite and rhyolite at contacts, concentric vesicle distribution, and crystal morphologies indicative of undercooling show that inclusions were incorporated in their rhyolitic hosts as blobs of magma. Inclusions were probably dispersed throughout small volumes of rhyolitic magma by convective (mechanical) mixing. Inclusion magma was formed by mixing (hybridization) at the interface between basaltic and rhyolitic magmas that coexisted in vertically zoned igneous systems. Relict phenocrysts and the bulk compositions of inclusions suggest that silicic endmembers were less differentiated than erupted high-silica rhyolite. Changes in inferred endmembers of magma mixtures with time suggest that the steepness of chemical gradients near the silicic/mafic interface in the zoned reservoir may have decreased as the system matured, although a high-silica rhyolitic cap persisted. The Coso example is an extreme case of large thermal and compositional contrast between inclusion and host magmas; lesser differences between intermediate composition magmas and inclusions lead to undercooling phenomena that suggest smaller ΔT. Vertical compositional zonation in magma chambers has been documented through study of products of voluminous pyroclastic eruptions. Magmatic inclusions in volcanic rocks provide evidence for compositional zonation and mixing processes in igneous systems when only lava is erupted.

California↗
USGS1984

Lead and strontium isotopic evidence for crustal interaction and compositional zonation in the source regions of Pleistocene basaltic and rhyolitic magmas of the Coso volcanic field, California

The isotopic compositions of Pb and Sr in Pleistocene basalt, high-silica rhyolite, and andesitic inclusions in rhyolite of the Coso volcanic field indicate that these rocks were derived from different levels of compositionally zoned magmatic systems. The 2 earliest rhyolites probably were tapped from short-lived silicic reservoirs, in contrast to the other 36 rhyolite domes and lava flows which the isotopic data suggest may have been leaked from the top of a single, long-lived magmatic system. Most Coso basalts show isotopic, geochemical, and mineralogic evidence of interaction with crustal rocks, but one analyzed flow has isotopic ratios that may represent mantle values (87Sr/86Sr=0.7036,206Pb/204Pb=19.05,207Pb/204Pb=15.62,208Pb/204Pb= 38.63). The (initial) isotopic composition of typical rhyolite (87Sr/86Sr=0.7053,206Pb/204Pb=19.29,207Pb/204Pb= 15.68,208Pb/204Pb=39.00) is representative of the middle or upper crust. Andesitic inclusions in the rhyolites are evidently samples of hybrid magmas from the silicic/mafic interface in vertically zoned magma reservoirs. Silicic end-member compositions inferred for these mixed magmas, however, are not those of erupted rhyolite but reflect the zonation within the silicic part of the magma reservoir. The compositional contrast at the interface between mafic and silicic parts of these systems apparently was greater for the earlier, smaller reservoirs.

Contributions to Mineralogy and Petrology↗
USGS1981

Oxygen isotope thermometry of basic lavas and mantle nodules

Measurements have been made of the oxygen isotope and chemical composition of glass and phenocrysts in lavas and coexisting minerals in mantle nodules. Temperatures of formation of these assemblages have been estimated from various chemical thermometers and range from 855?? to 1,300?? C. The permil fractionations between coexisting orthopyroxene and clinopyroxene in the lavas and nodules are all near zero. The fractionations between pyroxene and olivine vary from +1.2 to -1.4 and are a smooth function of temperature over the entire range. This function is given by T(?? C)=1151-173?? (px-d)-68??2(px-d) and has an uncertainty of ??60?? (2??). At temperatures above 1,150?? C, olivine in the nodules becomes more18O-rich than coexisting clinopyroxene, orthopyroxene, and plagioclase. In combination with the experimental work of Muehlenbachs and Kushiro (1974), the olivine-pyroxene fractionations indicate that olivine also becomes substantially more18O-rich than basaltic liquids above 1,200?? C. Geothermometers based on the oxygen isotope equilibration of basaltic liquid with olivine, pyroxene, and plagioclase are presented. ?? 1981 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1999

Understanding Vesuvius magmatic processes: Evidence from primitive silicate-melt inclusions in medieval scoria clinopyroxenes (Terzigno formation)

Microthermometric investigations of silicate-melt inclusions and electron microprobe analyses were conducted on experimentally homogenized silicate-melt inclusions and on the host clinopyroxenes from 4 scoria samples of different layers from the Mt. Somma-Vesuvius medieval eruption (Formazione di Terzigno, 893 A.D.). The temperature of homogenization, considered the minimum trapping temperature, ranges from 1190 to 1260 ± 5 °C for all clinopyroxene-hosted silicate melt inclusions. The major and minor-element compositional trends shown by Terzigno scoria and matrix glass chemical analysis are largely compatible with fractional crystallization of clinopyroxene and Fe-Ti oxides. Sulfur contents of the homogenized silicate-melt inclusions in clinopyroxene phenocrysts compared with that in the host scoria show that S has been significantly degassed in the erupted products; whereas, Cl has about the same abundance in the inclusions and in host scoria. Fluorine is low (infrequently up to 800 ppm) in the silicate-melt inclusions compared to 2400 ppm in the bulk scoria. Electron microprobe analyses of silicate-melt inclusions show that they have primitive magma compositions (Mg# = 75-91). The composition of the host clinopyroxene phenocrysts varies from typical plinian-related (Mg#≥85) to non plinian related (Mg#≤85). The mixed source of the host clinopyroxenes and primitive nature of the silicate-melt inclusions implies that these phenocrysts, in part, may be residual and/or have a polygenetic origin. The similar variation trends of major and minor-elements between homogenized silicate-melt inclusions from the Terzigno scoria, and silicate-melt inclusions in olivine and diopside phenocrysts from plinian eruptions ( Marianelli et al., 1995) suggest that the trapped inclusions represent melts similar to those that supplied the plinian and sub-plinian magma chambers. These geochemical characteristics suggest that the Vesuvius magmatic system retained a vestige of the most recent plinian event.

Mt. Somma-Vesuvius↗
USGS1995

Mineralogical and geochemical evolution of micas from miarolitic pegmatites of the anorogenic pikes peak batholith, Colorado

A suite of 29 micas from miarolitic pegmatites associated with granitic units of the anorogenic Pikes Peak batholith (1.08-1.02 Ga), Colorado range in composition, and follow in paragenetic sequence, from 1M siderophyllite (N = 1), and 3T or 2M1 lithian biotite (N = 5) to 1M zinnwaldite (N = 20) and 1M ferroan lepidolite (N = 1). Locally, 1M (?) phlogopite (N = 1) and ferroan 2M1 muscovite (N = 1) are also present. Pervasive, late-stage hydrothermal alteration along with possible supergene weathering of many of these micas produced vermiculite. Additionally, some vugs and cavities were filled with chlorite and/or smectite. Early crystallized micas form tapered columnar crystals in graphic pegmatite, growing toward, and adjacent to the miarolitic cavity zone which contains the later crystallized micas. Principal associated minerals are quartz, microcline perthite (mostly amazonite), and albite, with local topaz or fluorite, and rarely tourmaline (schorl-elbaite). Progressively younger micas of the main crystallization sequence display increasing Si, Li, F, and Al/Ga, and decreasing total Fe, Mg, and octahedral occupancy. The zinc content of all micas is considerably elevated, whereas Mn, Rb, Cs, and Sc are moderate and T1 is very low. Early siderophyllite and lithian biotite show a narrow range of FeO/Fe2O3 (5.6-8.0), whereas later zinnwaldite is much more variable (2.4-40.3). Annite of the host granite and early graphic pegmatite is compositionally homogeneous, but most mica crystals from cavities show remarkable compositional and abrupt, sharp and distinct color zoning. Most cavity-grown zinnwaldite crystals show a decrease, from core to rim, in total Fe and Mg, whereas Si, Li and F increase and Mn, Rb, Cs and Na are essentially constant. A few to more than 100 color zones have been identified in some mica crystals. The zones are well correlated with the Ti content (<0.2 wt. % TiO2 colorless, 0.4-0.6 wt.% TiO2 red-brown). The total Fe content may or may not correlate with color zoning, whereas Zn variations (up to 1.1 wt. %) are entirely independent. The dark color zones probably reflect Fe-Ti charge transfer. The mica composition sequence described here is typical of the extreme fractionation observed in pegmatites of the NYF family, associated with anorogenec granites. Elevated Fe, Zn, and enhanced Sc contents are characteristic of this family. Strong enrichment in Li, Rb, and F is present, particularly in the micas of the miarolitic cavities. Sharp color zonation and compositional variation in cavity-grown zinnwaldite and ferroan lepidolite crystals suggest rapid changes in the intensive parameters, particularly the f(O2), of the parent fluid during the final stages of pegmatite consolidation ?? 1995 Springer-Verlag.

Mineralogy and Petrology↗
USGS1987

Residence of silver in mineral deposits of the Thunder Mountain caldera complex, Central Idaho, U.S.A.

Silver is an accessory element in gold, antimony, and tungsten deposits of the caldera complex. Most of the deposits are economically of low grade and genetically of xenothermal or epithermal character. Their gold- and silver-bearing minerals are usually disseminated, fine grained, and difficult to study. Sparsely disseminated pyrite and arsenoprite are common associates. Identified silver minerals are: native silver and electrum; the sulfides acanthite, argentite (the latter always inverted to acanthite), and members of the Silberkies group; the sulfosalts matildite, miargyrite, pyrargyrite, argentian tetrahedrite, and unnamed Ag-Sb-S and Ag-Fe-Sb-S minerals; the telluride hessite and the selenide naumannite; halides of the cerargyrite group; and the antimonate stetefeldtite. Suspected silver minerals include the sulfide uytenbogaardtite and the sulfosalts andorite, diaphorite, and polybasite. Electrum, acanthite, and argentian tetrahedrite are common, though nowhere abundant. The other silver minerals are rare. Silver is present as a minor element in the structure of some varieties of other minerals. These include arsenopyrite, chalcopyrite, chalcostibite, covelline, digenite, galena, sphalerite, and stibnite. The search for adventitious Ag in most of these minerals has been cursory. The results merely indicate that elemental silver is not confined to discrete silver minerals and is, therefore, an additional complication for the recovery of silver-bearing material from some deposits. Silver occurs cryptically in some plants of the region. At Red Mountain, for example, the ashed sapwood of Douglas-fir (Pseudotsuga menziesii) contains 2 to 300 ppm Ag. Silver in the ashed wood is roughly 100 times as abundant as it is in soil. The phenomenon, useful in biogeochemical exploration, deserves the attention of mineralogists. ?? 1987 Springer-Verlag.

Mineralogy and Petrology↗
USGS1979

Rare earth abundances and Rb-Sr systematics of basalts, gabbro, anorthosite and minor granitic rocks from the Indian Ocean Ridge System, Western Indian Ocean

Basalts dredged from the Mid-Indian Ocean Ridge System have rare earth, Rb, and Sr concentrations like those from other mid-ocean ridges, but have slightly higher Sr87/Sr86 ratios. Underlying gabbroic complexes are similar to the basalts in Sr87/Sr86, but are poorer K, Rb, and in rare earths. The chemical and isotopic data, as well as the geologic relations suggest a cumulate origin for the bulk of the gabbroic complexes. ?? 1979 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1979

An evaluation of the zircon method of isotopic dating in the Southern Arabian Craton

A zircon study has been made on eleven samples of igneous rocks from the Saudi Arabian Craton. Ages of sized and magnetic fractions of zircon concentrates show variable degrees of discordance which seem to result from a very young disturbance that produces linear arrays in the Concordia plot. Model age calculations based on a statistically and geologically reasonable lower intercept produce very consistent internal relationships. The Pan African Orogeny, considered to be responsible for loss of radiogenic argon and strontium from minerals of many rocks, does not appear to have affected the zircon data, even though uplift had exposed the rocks of the Arabian Shield at that time. Tonalite, granodiorite, and crosscutting leucoadamellite bodies in the southern part of the An Nimas Bathylith yield ages in the time range 820-760 Ma. A narrow time range of 660 to 665 million years was indicated for ages of widely separated and compositionally different intrusive bodies all to the east of the An Nimas Bathylith. This work suggests that the younger end of the age spectrum established from regional K-Ar and Rb-Sr measurements may be underestimated, and that magmatic activity could be more episodic than previously assumed.

Contributions to Mineralogy and Petrology↗
USGS1981

A routine high-precision method for Lu-Hf isotope geochemistry and chronology

A method for chemical separation of Lu and Hf from rock, meteorite and mineral samples is described, together with a much improved mass spectrometric running technique for Hf. This allows (i) geo- and cosmochronology using the176Lu???176Hf+??- decay scheme, and (ii) geochemical studies of planetary processes in the earth and moon. Chemical yields for the three-stage ion-exchange column procedure average 90% for Hf. Chemical blanks are <0.2 ng for Lu and Hf. From 1 ??g of Hf, a total ion current of 0.5??10-11 Ampere can be maintained for 3-5 h, yielding 0.01-0.03% precision on the ratio176Hf/177Hf. Normalisation to179Hf/177Hf=0.7325 is used. Extensive results for the Johnson Matthey Hf standard JMC 475 are presented, and this sample is urged as an international mass spectrometric standard; suitable aliquots, prepared from a single batch of JMC 475, are available from Denver. Lu-Hf analyses of the standard rocks BCR-1 and JB-1 are given. The potential of the Lu-Hf method in isotope geochemistry is assessed. ?? 1980 Springer-Verlag.

Contributions to Mineralogy and Petrology↗