Geology topics

J.D. Webster

Publications and source records attributed to J.D. Webster.

6 recordsLinked to original sources

USGS2011

Formation of cordierite-bearing lavas during anatexis in the lower crust beneath Lipari Island (Aeolian arc, Italy)

Cordierite-bearing lavas (CBL;~105 ka) erupted from the Mt. S. Angelo volcano at Lipari (Aeolian arc, Italy) are high-K andesites, displaying a range in the geochemical and isotopic compositions that reflect heterogeneity in the source and/or processes. CBL consist of megacrysts of Ca-plagioclase and clinopyroxene, euhedral crystals of cordierite and garnet, microphenocrysts of orthopyroxene and plagioclase, set in a heterogeneous rhyodacitic-rhyolitic groundmass containing abundant metamorphic and gabbroic xenoliths. New petrographic, chemical and isotopic data indicate formation of CBL by mixing of basaltic-andesitic magmas and high-K peraluminous rhyolitic magmas of anatectic origin and characterize partial melting processes in the lower continental crust of Lipari. Crustal anatectic melts generated through two main dehydration-melting peritectic reactions of metasedimentary rocks: (1) Biotite + Aluminosilicate + Quartz + Albite = Garnet + Cordierite + K-feldspar + Melt; (2) Biotite + Garnet + Quartz = Orthopyroxene + Cordierite + K-feldspar + Melt. Their position into the petrogenetic grid suggests that heating and consequent melting of metasedimentary rocks occurred at temperatures of 725 < T < 900°C and pressures of 0.4–0.45 GPa. Anatexis in the lower crust of Lipari was induced by protracted emplacement of basic magmas in the lower crust (~130 Ky). Crustal melting of the lower crust at 105 ka affected the volcano evolution, impeding frequent mafic-magma eruptions, and promoting magma stagnation and fractional crystallization processes.

Contributions to Mineralogy and Petrology↗

USGS2009

Stable isotope and petrologic evidence for open-system degassing during the climactic and pre-climactic eruptions of Mt. Mazama, Crater Lake, Oregon

Evaluation of the extent of volatile element recycling in convergent margin volcanism requires delineating likely source(s) of magmatic volatiles through stable isotopic characterization of sulfur, hydrogen and oxygen in erupted tephra with appropriate assessment of modification by degassing. The climactic eruption of Mt. Mazama ejected approximately 50 km 3 of rhyodacitic magma into the atmosphere and resulted in formation of a 10-km diameter caldera now occupied by Crater Lake, Oregon (lat. 43°N, long. 122°W). Isotopic compositions of whole-rocks, matrix glasses and minerals from Mt. Mazama climactic, pre-climactic and postcaldera tephra were determined to identify the likely source(s) of H 2 O and S. Integration of stable isotopic data with petrologic data from melt inclusions has allowed for estimation of pre-eruptive dissolved volatile concentrations and placed constraints on the extent, conditions and style of degassing. Sulfur isotope analyses of climactic rhyodacitic whole rocks yield δ 34 S values of 2.8–14.8‰ with corresponding matrix glass values of 2.4–13.2‰. δ 34 S tends to increase with stratigraphic height through climactic eruptive units, consistent with open-system degassing. Dissolved sulfur concentrations in melt inclusions (MIs) from pre-climactic and climactic rhyodacitic pumices varies from 80 to 330 ppm, with highest concentrations in inclusions with 4.8–5.2 wt% H 2 O (by FTIR). Up to 50% of the initial S may have been lost through pre-eruptive degassing at depths of 4–5 km. Ion microprobe analyses of pyrrhotite in climactic rhyodacitic tephra and andesitic scoria indicate a range in δ 34 S from −0.4‰ to 5.8‰ and from −0.1‰ to 3.5‰, respectively. Initial δ 34 S values of rhyodacitic and andesitic magmas were likely near the mantle value of 0‰. Hydrogen isotope (δD) and total H 2 O analyses of rhyodacitic obsidian (and vitrophyre) from the climactic fall deposit yielded values οf −103 to −53‰ and 0.23–1.74 wt%, respectively. Values of δD and wt% H 2 O of obsidian decrease towards the top of the fall deposit. Samples with depleted δD, and mantle δ 18 O values, have elevated δ 34 S values consistent with open-system degassing. These results imply that more mantle-derived sulfur is degassed to the Earth’s atmosphere/hydrosphere through convergent margin volcanism than previously attributed. Magmatic degassing can modify initial isotopic compositions of sulfur by >14‰ (to δ 34 S values of 14‰ or more here) and hydrogen isotopic compositions by 90‰ (to δD values of −127‰ in this case).

Oregon↗

USGS1998

Pre-eruptive volatile content, melt-inclusion chemistry, and microthermometry of interplinian Vesuvius lavas (pre-AD 1631)

Silicate-melt inclusions from lavas and pyroclastics from a selected suite of pre-A.D. 1631 interplinian Mt. Somma-Vesuvius lavas and scoria have been experimentally homogeneized and studied by microthermometry, electron microprobe (EMPA) and secondary-ion mass spectrometry (SIMS) to examine pre-eruptive volatile content and magma evolution. The melt inclusions have a bubble about 0.06% their volume, uncommonly contain non-condensable gas but do not contain any dense fluid phases. Clinopyroxene-hosted inclusions yield homogenization temperatures (Th) from 1170 to 1260??C, most between 1220 and 1240??C; plagiclase-hosted inclusions have Th from 1210 to 1230??C; these values are typical for the Vesuvius environment. The dominant factor controlling major element variability in the inclusions is clinopyroxene fractionation; MgO varies from 5 to 3 wt%, SiO2 varies from 60 to 48 wt%. total alkalis vary from 15 to 4 wt%, and CaO varies from 13 to 5 wt%. H2O varies from 2.7 to 0.6 wt% and is decoupled from incompatible element evolution suggesting vapor saturation during trapping. Chlorine and F vary from 1.- wt% to 0 and 0.63 to 0 wt%, respectively. Bulk rock and limited matrix glass analyses show that the lavas lost about half of their F and Cl content except for the A.D. 472-1631 lava which contains similar Cl abundances as the bulk rock. SO3 varies from 0.5 to 0 wt% and compared with matrix glass and bulk rock demonstrate that the lavas have lost essentially all sulfur. The samples can be classified into three age groups, ??? 25 000 yr B.P., 25 000-17 000 yr B.P., and A.D. 472-1631. There is a systematic increase in some components, e.g., total alkalis, SO3, Cl, Li, B, and Sr with the youth of the sample and a decrease in others, e.g., Zr and Y. However, on average these samples seem less evolved than later A.D. 1631-1944 lavas.

Journal of Volcanology and Geothermal Research↗

USGS1995

Roof-rock contamination of magma along the top of the reservoir for the Bishop Tuff

The Bishop Tuff, a Quaternary high-silica rhyolite in east-central California, is widely considered the type example of a vertically and monotonically zoned pyroclastic deposit that represents zoning in the source magma reservoir, inverted during the process of pyroclastic emplacement. However, the deposit of plinian pumice, which forms the base of the Bishop Tuff and represents the initial 10% or so of all magma erupted during the event that produced the Bishop Tuff, contains features at odds with monotonic zoning for the reservoir. Relative to overlying ignimbrite, the plinian deposit contains a reversal in trace-element zoning. The data have been previously interpreted as due to processes of chemical fractionation and evolution operating within a magma system closed to chemical interactions with its roof rocks. However, it is suggested here that the reversed zoning and other above-noted features can be explained equally well as consequences of minor assimilation of roof rocks into a magma reservoir that was erupted from the top down. -from Authors

Journal of Volcanology and Geothermal Research↗

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↗

USGS1984

U-Pb isotope systematics and apparent ages of uranium ores, Ambrosia Lake and Smith Lake districts, Grants mineral belt, New Mexico

Orebodies occur in continental sandstones of the Upper Jurassic Morrison Formation and comprise two main types of mineralization; primary ore formed early in the history of the host rock and resulted in tabular, peneconcordant orebodies rich in organic material; redistributed ore apparently was formed by oxidative destruction and reconcentration of primary ore at some time after Laramide deformation and resulted in roll-type orebodies lacking organic material. U-Pb isotope ages of four redistributed ores from the Ambrosia Lake District give concordant to nearly concordant ages of 3.3 to 12.5 m.y., supporting the concept that most redistributed ore formed in the late Tertiary or later. U-Pb isotope ages of primary ores from the Ambrosia Lake District show pronounced normal discordance, evidently due to coupled, continuous loss of Pb and radioactive daughters of 238 U. Data for ores from the Smith Lake District consistently give pre-Tertiary apparent ages.

Economic Geology↗