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At least 163 records · Page 9Linked to original sources
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

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↗
USGS1967

The role of olivine in the crystallization of the prehistoric Makaopuhi tholeiitic lava lake, Hawaii

On eruption, the tholeiitic basalt lava of the prehistoric Makaopuhi lake contained nearly seven percent euhedral olivine phenocrysts of approximately Fa 14 composition. In the center of the 225 foot vertical section of the lake, the lava became more than 90 percent solid at 1000° C after about 30 years. At the surface the lava was quenched to air temperature, whereas, at the bottom, quenching to 800° C was followed by a 40 year period before the temperature reached 700° C. The olivine phenocrysts settled at an average rate of about 4 × 10 −6 cm Sec −1 to form a zone that contains 21 percent olivine 75 feet above the base. Sinking of olivines continued until some time after the beginning of the crystallization of augite and plagioclase. Thin rims of iron-rich olivine (up to Fa 55 ) surrounding the phenocrysts, and a second generation of fine-grained olivines (Fa 20 Fa 48 ) restricted to the uppermost 20 feet indicate local extensions of the period of crystallization of olivine. During crystallization of the groundmass and later subsolidus cooling in the range 1000° C to at least as low as 800° C, the olivine phenocrysts were converted to Fa 30–40 by interdiffusion of Fe, Mg, Ni, and Mn. Homogenization of Mg-rich cores and Fe-rich margins and equilibration of olivine composition with the groundmass phases was progressively less well achieved toward the top of the lake. Reaction rims around the olivines are composed primarily of Ca-rich pyroxene. Pigeonite crystallized alongside augite except in the uppermost 5 feet where there is abundant ground mass olivine. Poikilitic hypersthene grew at the expense of pre-existing ferromagnesian minerals in the cumulate zone.

Hawaii↗
USGS1984

Great Salt Lake, and precursors, Utah: The last 30,000 years

Sediment cores up to 6.5 m in length from the South Arm of Great Salt Lake, Utah, have been correlated. Radiocarbon ages and volcanic tephra layers indicate a record of greater than 30,000 years. A variety of approaches have been employed to collect data used in stratigraphic correlation and lake elevation interpretation; these include acoustic stratigraphy, sedimentologic analyses, mineralogy, geochemistry (major element, C, O and S isotopes, and organics), paleontology and pollen. The results indicate that prior to 32,000 year B.P. an ephemeral saline lake-playa system was present in the basin. The perennial lake, which has occupied the basin since this time, rose in a series of three major steps; the freshest water conditions and presumably highest altitude was reached at about 17,000 year B.P. The lake remained fresh for a brief period, followed by a rapid increase in salinity and sharp lowering in elevation to levels below that of the present Great Salt Lake. The lake remained at low elevations, and divided at times into a north and south Basin, until about 8,000 year B.P. Since that time, with the exception of two short rises to about 1290 m, the lake level has remained near the present elevation of 1280 m. ?? 1984 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1990

Partitioning of F between H2O and CO2 fluids and topaz rhyolite melt - Implications for mineralizing magmatic-hydrothermal fluids in F-rich granitic systems

Fluid/melt distribution coefficients for F have been determined in experiments conducted with peraluminous topaz rhyolite melts and fluids consisting of H2O and H2O+CO2 at pressures of 0.5 to 5 kbar, temperatures of 775??-1000??C, and concentrations of F in the melt ranging from 0.5 to 6.9 wt%. The major element, F, and Cl concentrations of the starting material and run product glasses were determined by electron microprobe, and the concentration of F in the fluid was calculated by mass balance. The H2O concentrations of some run product glasses were determined by ion microprobe (SIMS). The solubility of melt in the fluid phase increases with increasing F in the system; the solubility of H2O in the melt is independent of the F concentration of the system with up to 6.3 wt% F in the melt. No evidence of immiscible silica- and fluoriderich liquids was detected in the hydrous but water-undersaturated starting material glasses (???8.5 wt% F in melt) or in the water-saturated run product glasses. F concentrates in topaz rhyolite melts relative to coexisting fluids at most conditions studied; however, DF (wt% F in fluid/wt% F in melt) increases strongly with increasing F in the system. Maximum values of DF in this study are significantly larger than those previously reported in the literature. Linear extrapolation of the data suggests that DF is greater than one for water-saturated, peraluminous granitic melts containing ???8 wt% F at 800?? C and 2 kbar. DF increases as temperature and as (H2O/H2O+CO2) of the fluid increase. For topaz rhyolite melts containing ???1 wt% F and with H2O-rich fluids, DF is independent of changes in pressure from 2 to 5 kbar at 800?? C; for melts containing ???1 wt% F and in equilibrium with CO2-bearing fluids the concentrations of F in fluid increases with increasing pressure. F-and lithophile element-enriched granites may evolve to compositions containing extreme concentrations of F during the final stages of crystallization. If F in the melt exceeds 8 wt%, DF is greater than one and the associated magmatic-hydrothermal fluid contains >4 molal F. Such F-enriched fluids may be important in the mass transport of ore constituents, i.e., F, Mo, W, Sn, Li, Be, Rb, Cs, U, Th, Nb, Ta, and B, from the magma. ?? 1990 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS2002

Magma storage prior to the 1912 eruption at Novarupta, Alaska

New analytical and experimental data constrain the storage and equilibration conditions of the magmas erupted in 1912 from Novarupta in the 20th century's largest volcanic event. Phase relations at H 2 O+CO 2 fluid saturation were determined for an andesite (58.7 wt% SiO 2 ) and a dacite (67.7 wt%) from the compositional extremes of intermediate magmas erupted. The phase assemblages, matrix melt composition and modes of natural andesite were reproduced experimentally under H 2 O-saturated conditions (i.e., P H2O =P TOT ) in a negatively sloping region in T-P space from 930 ° C/100 MPa to 960 ° C/75 MPa with f O 2 ~N NO + 1. The H 2 O-saturated equilibration conditions of the dacite are constrained to a T-P region from 850 ° C/ 50 MPa to 880 ° C/25 MPa. If H 2 O-saturated, these magmas equilibrated at (and above) the level where coerupted rhyolite equilibrated (~100 MPa), suggesting that the andesite-dacite magma reservoir was displaced laterally rather than vertically from the rhyolite magma body. Natural mineral and melt compositions of intermediate magmas were also reproduced experimentally under saturation conditions with a mixed (H 2 O + CO 2 ) fluid for the same range in P H2O . Thus, a storage model in which vertically stratified mafic to silicic intermediate magmas underlay H 2 O-saturated rhyolite is consistent with experimental findings only if the intermediates have X H2O fl=0.7 and 0.9 for the extreme compositions, respectively. Disequilibrium features in natural pumice and scoria include pristine minerals existing outside their stability fields, and compositional zoning of titanomagnetite in contact with ilmenite. Variable rates of chemical equilibration which would eliminate these features constrain the apparent thermal excursion and re-distribution of minerals to the time scale of days.

Alaska↗
USGS2004

Rear-arc vs. arc-front volcanoes in the Katmai reach of the Alaska Peninsula: A critical appraisal of across-arc compositional variation

Physical and compositional data and K-Ar ages are reported for 14 rear-arc volcanoes that lic 11-22 km behind the narrowly linear volcanic front defined by the Mount Katmai-to-Devils Desk chain on the Alaska Peninsula. One is a 30-km3 stratocone (Mount Griggs; 51-63% SiO2) active intermittently from 292 ka to Holocene. The others are monogenetic cones, domes, lava flows, plugs, and maars, of which 12 were previously unnamed and unstudied; they include seven basalts (48-52% SiO2), four mafic andesites (53-55% SiO2), and three andesite-dacite units. Six erupted in the interval 500-88 ka, one historically in 1977, and five in the interval 3-2 Ma. No migration of the volcanic front is discernible since the late Miocene, so even the older units erupted well behind the front. Discussion explores the significance of the volcanic front and the processes that influence compositional overlaps and differences among mafic products of the rear-arc volcanoes and of the several arc-front edifices nearby. The latter have together erupted a magma volume of about 200 km3, at least four times that of all rear-arc products combined. Correlation of Sr-isotope ratios with indices of fractionation indicates crustal contributions in volcanic-front magmas (0.7033-0.7038), but lack of such trends among the rear-arc units (0.70298-0.70356) suggests weaker and less systematic crustal influence. Slab contributions and mantle partial-melt fractions both appear to decline behind the front, but neither trend is crisp and unambiguous. No intraplate mantle contribution is recognized nor is any systematic across-arc difference in intrinsic mantle-wedge source fertility discerned. Both rear-arc and arc-front basalts apparently issued from fluxing of typically fertile NMORB-source mantle beneath the Peninsular terrane, which docked here in the Mesozoic. Springer-Verlag 2004.

Alaska↗
USGS2005

Experimental and geochemical evidence for derivation of the El Capitan Granite, California, by partial melting of hydrous gabbroic lower crust

Partial melting of mafic intrusions recently emplaced into the lower crust can produce voluminous silicic magmas with isotopic ratios similar to their mafic sources. Low-temperature (825 and 850°C) partial melts synthesized at 700 MPa in biotite-hornblende gabbros from the central Sierra Nevada batholith (Sisson et al. in Contrib Mineral Petrol 148:635–661, 2005) have major-element and modeled trace-element (REE, Rb, Ba, Sr, Th, U) compositions matching those of the Cretaceous El Capitan Granite, a prominent granite and silicic granodiorite pluton in the central part of the Sierra Nevada batholith (Yosemite, CA, USA) locally mingled with coeval, isotopically similar quartz diorite through gabbro intrusions (Ratajeski et al. in Geol Soc Am Bull 113:1486–1502, 2001). These results are evidence that the El Capitan Granite, and perhaps similar intrusions in the Sierra Nevada batholith with lithospheric-mantle-like isotopic values, were extracted from LILE-enriched, hydrous (hornblende-bearing) gabbroic rocks in the Sierran lower crust. Granitic partial melts derived by this process may also be silicic end members for mixing events leading to large-volume intermediate composition Sierran plutons such as the Cretaceous Lamarck Granodiorite. Voluminous gabbroic residues of partial melting may be lost to the mantle by their conversion to garnet-pyroxene assemblages during batholithic magmatic crustal thickening.

Contributions to Mineralogy and Petrology↗
USGS2006

Platinum-group element, Gold, Silver and Base Metal distribution in compositionally zoned sulfide droplets from the Medvezky Creek Mine, Noril'sk, Russia

Concentrations of Ag, Au, Cd, Co, Re, Zn and Platinum-group elements (PGE) have been determined in sulfide minerals from zoned sulfide droplets of the Noril'sk 1 Medvezky Creek Mine. The aims of the study were; to establish whether these elements are located in the major sulfide minerals (pentlandite, pyrrhotite, chalcopyrite and cubanite), to establish whether the elements show a preference for a particular sulfide mineral and to investigate the model, which suggests that the zonation in the droplets is caused by the crystal fractionation of monosulfide solid solution (mss). Nickel, Cu, Ag, Re, Os, Ir, Ru, Rh and Pd, were found to be largely located in the major sulfide minerals. In contrast, less than 25% of the Au, Cd, Pt and Zn in the rock was found to be present in these sulfides. Osmium, Ir, Ru, Rh and Re were found to be concentrated in pyrrhotite and pentlandite. Palladium and Co was found to be concentrated in pentlandite. Silver, Cd and Zn concentrations are highest in chalcopyrite and cubanite. Gold and platinum showed no preference for any of the major sulfide minerals. The enrichment of Os, Ir, Ru, Rh and Re in pyrrhotite and pentlandite (exsolution products of mss) and the low levels of these elements in the cubanite and chalcopyrite (exsolution products of intermediate solid solution, iss) support the mss crystal fractionation model, because Os, Ir, Ru, Rh and Re are compatible with mss. The enrichment of Ag, Cd and Zn in chalcopyrite and cubanite also supports the mss fractionation model these minerals are derived from the fractionated liquid and these elements are incompatible with mss and thus should be enriched in the fractionated liquid. Gold and Pt do not partition into either iss or mss and become sufficiently enriched in the final fractionated liquid to crystallize among the iss and mss grains as tellurides, bismithides and alloys. During pentlandite exsolution Pd appears to have diffused from the Cu-rich portion of the droplet into pentlandite. ?? Springer-Verlag 2006.

Contributions to Mineralogy and Petrology↗
USGS2008

Isotopic and trace element constraints on the petrogenesis of lavas from the Mount Adams volcanic field, Washington

Strontium, Nd, Pb, Hf, Os, and O isotope compositions for 30 Quaternary lava flows from the Mount Adams stratovolcano and its basaltic periphery in the Cascade arc, southern Washington, USA indicate a major component from intraplate mantle sources, a relatively small subduction component, and interaction with young mafic crust at depth. Major- and trace-element patterns for Mount Adams lavas are distinct from the rear-arc Simcoe volcanic field and other nearby volcanic centers in the Cascade arc such as Mount St. Helens. Radiogenic isotope (Sr, Nd, Pb, and Hf) compositions do not correlate with geochemical indicators of slab-fluids such as (Sr/P)n and Ba/Nb. Mass-balance modeling calculations, coupled with trace-element and isotopic data, indicate that although the mantle source for the calc-alkaline Adams basalts has been modified with a fluid derived from subducted sediment, the extent of modification is significantly less than what is documented in the southern Cascades. The isotopic and trace-element compositions of most Mount Adams lavas require the presence of enriched and depleted mantle sources, and based on volume-weighted chemical and isotopic compositions for Mount Adams lavas through time, an intraplate mantle source contributed the major magmatic mass of the system. Generation of basaltic andesites to dacites at Mount Adams occurred by assimilation and fractional crystallization in the lower crust, but wholesale crustal melting did not occur. Most lavas have Tb/Yb ratios that are significantly higher than those of MORB, which is consistent with partial melting of the mantle in the presence of residual garnet. 18O values for olivine phenocrysts in Mount Adams lavas are within the range of typical upper mantle peridotites, precluding involvement of upper crustal sedimentary material or accreted terrane during magma ascent. The restricted Nd and Hf isotope compositions of Mount Adams lavas indicate that these isotope systems are insensitive to crustal interaction in this juvenile arc, in stark contrast to Os isotopes, which are highly sensitive to interaction with young, mafic material in the lower crust. Springer-Verlag 2008.

Washington↗
USGS2009

Accessory mineral U–Th–Pb ages and 40Ar/39Ar eruption chronology, and their bearing on rhyolitic magma evolution in the Pleistocene Coso volcanic field, California

We determined Ar/Ar eruption ages of eight extrusions from the Pleistocene Coso volcanic field, a long-lived series of small volume rhyolitic domes in eastern California. Combined with ion-microprobe dating of crystal ages of zircon and allanite from these lavas and from granophyre geothermal well cuttings, we were able to track the range of magma-production rates over the past 650 ka at Coso. In ≤230 ka rhyolites we find no evidence of protracted magma residence or recycled zircon (or allanite) from Pleistocene predecessors. A significant subset of zircon in the ~85 ka rhyolites yielded ages between ~100 and 200 Ma, requiring that generation of at least some rhyolites involves material from Mesozoic basement. Similar zircon xenocrysts are found in an ~200 ka granophyre. The new age constraints imply that magma evolution at Coso can occur rapidly as demonstrated by significant changes in rhyolite composition over short time intervals (≤10’s to 100’s ka). In conjunction with radioisotopic age constraints from other young silicic volcanic fields, dating of Coso rhyolites highlights the fact that at least some (and often the more voluminous) rhyolites are produced relatively rapidly, but that many small-volume rhyolites likely represent separation from long-lived mushy magma bodies.

California↗
USGS2009

On the occurrence, trace element geochemistry, and crystallization history of zircon from in situ ocean lithosphere

We characterize the textural and geochemical features of ocean crustal zircon recovered from plagiogranite, evolved gabbro, and metamorphosed ultramafic host-rocks collected along present-day slow and ultraslow spreading mid-ocean ridges (MORs). The geochemistry of 267 zircon grains was measured by sensitive high-resolution ion microprobe-reverse geometry at the USGS-Stanford Ion Microprobe facility. Three types of zircon are recognized based on texture and geochemistry. Most ocean crustal zircons resemble young magmatic zircon from other crustal settings, occurring as pristine, colorless euhedral (Type 1) or subhedral to anhedral (Type 2) grains. In these grains, Hf and most trace elements vary systematically with Ti, typically becoming enriched with falling Ti-in-zircon temperature. Ti-in-zircon temperatures range from 1,040 to 660°C (corrected for a TiO2 ≈ 0.7, a SiO2 ≈ 1.0, pressure ≈ 2 kbar); intra-sample variation is typically ~60–150°C. Decreasing Ti correlates with enrichment in Hf to ~2 wt%, while additional Hf-enrichment occurs at relatively constant temperature. Trends between Ti and U, Y, REE, and Eu/Eu* exhibit a similar inflection, which may denote the onset of eutectic crystallization; the inflection is well-defined by zircons from plagiogranite and implies solidus temperatures of ~680–740°C. A third type of zircon is defined as being porous and colored with chaotic CL zoning, and occurs in ~25% of rock samples studied. These features, along with high measured La, Cl, S, Ca, and Fe, and low (Sm/La) N ratios are suggestive of interaction with aqueous fluids. Non-porous, luminescent CL overgrowth rims on porous grains record uniform temperatures averaging 615 ± 26°C (2SD, n = 7), implying zircon formation below the wet-granite solidus and under water-saturated conditions. Zircon geochemistry reflects, in part, source region; elevated HREE coupled with low U concentrations allow effective discrimination of ~80% of zircon formed at modern MORs from zircon in continental crust. The geochemistry and textural observations reported here serve as an important database for comparison with detrital, xenocrystic, and metamorphosed mafic rock-hosted zircon populations to evaluate provenance.

Contributions to Mineralogy and Petrology↗
USGS2009

Basanite-nephelinite suite from early Kilauea: Carbonated melts of phlogopite-garnet peridotite at Hawaii's leading magmatic edge

A basanite-nephelinite glass suite from early submarine Kilauea defines a continuous compositional array marked by increasing concentrations of incompatible components with decreasing SiO 2 , MgO, and Al 2 O 3 . Like peripheral and post-shield strongly alkalic Hawaiian localities (Clague et al. in J Volcanol Geotherm Res 151:279-307, 2006; Dixon et al. in J Pet 38:911-939, 1997), the early Kilauea basanite-nephelinite glasses are interpreted as olivine fractionation products from primary magnesian alkalic liquids. For early Kilauea, these were saturated with a garnet-phlogopite-sulfide peridotite assemblage, with elevated dissolved CO 2 contents responsible for the liquids' distinctly low-SiO 2 concentrations. Reconstructed primitive liquids for early Kilauea and other Hawaiian strongly alkalic localities are similar to experimental 3 GPa low-degree melts of moderately carbonated garnet lherzolite, and estimated parent magma temperatures of 1,350-1,400??C (olivine-liquid geothermometry) match the ambient upper mantle geotherm shortly beneath the base of the lithosphere. The ???3 GPa source regions were too hot for stable crystalline carbonate and may have consisted of ambient upper mantle peridotite containing interstitial carbonate-silicate or carbonatitic liquid, possibly (Dixon et al. in Geochem Geophys Geosyst 9(9):Q09005, 2008), although not necessarily, from the Hawaiian mantle plume. Carbonate-enriched domains were particularly susceptible to further melting upon modest decompression during upward lithospheric flexure beneath the advancing Hawaiian Arch, or by conductive heating or upward drag by the Hawaiian mantle plume. The early Kilauea basanite-nephelinite suite has a HIMU-influenced isotopic character unlike other Hawaiian magmas (Shimizu et al. in EOS Tran Amer Geophys Union 82(47): abstr V12B-0962, 2001; Shimizu et al. in Geochim Cosmochim Acta 66(15A):710, 2002) but consistent with oceanic carbonatite involvement (Hoernle et al. in Contrib Mineral Petrol 142:520-542, 2002). It may represent the melting products of a fertile domain in the ambient upper mantle impinged upon and perturbed by the sustained plume source that feeds later shield-stage magmatism. ?? US Government 2009.

Contributions to Mineralogy and Petrology↗
USGS2010

Zircon-scale insights into the history of a Supervolcano, Bishop Tuff, Long Valley, California, with implications for the Ti-in-zircon geothermometer

Zircon has the outstanding capacity to record chronological, thermal, and chemical information, including the storage history of zoned silicic magma reservoirs like the one responsible for the Bishop Tuff of eastern California, USA. Our novel ion microprobe approach reveals that Bishop zircon rims with diverse chemical characteristics surround intermediate domains with broadly similar compositions. The highest Y, REE, U, and Th concentrations tend to accompany the largest excesses in Y + REE3+:P beyond what can be explained by xenotime substitution in zircon. Apparent Ti-in-zircon temperatures of <720??C for zircon rims are distinctly lower than most of the range in eruption temperatures, as estimated from FeTi-oxide equilibria and zircon solubility at quench. While permissive of crystallization of zircon at near-solidus conditions, the low Ti-in-zircon temperatures are probably better explained by sources of inaccuracy in the temperature estimates. After apparently nucleating from different melts, zircons from across the Bishop Tuff compositional spectrum may have evolved to broadly similar chemical and thermal conditions and therefore it is possible that there was no significant thermal gradient in the magma reservoir at some stage in its evolution. There is also no compelling evidence for punctuated heat ?? chemical influxes during the intermediate stages of zircon growth. Judging by the zircon record, the main volume of the erupted magma evolved normally by secular cooling but the latest erupted portion is characterized by a reversal in chemistry that appears to indicate perfusion of the magma reservoir by-or zircon entrainment in-a less evolved melt from the one in which the zircons had previously resided. ?? 2010 Springer-Verlag.

Contributions to Mineralogy and Petrology↗