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At least 343 records · Page 19Linked to original sources

USGS1976

Serpentinization and alteration in an olivine cumulate from the Stillwater Complex, Southwestern Montana

Some of the olivine cumulates of the Ultramafic zone of the Stillwater Complex, Montana, are progressively altered to serpentine minerals and thompsonite. Lizardite and chrysotile developed in the cumulus olivine and postcumulus pyroxenes; thompsonite developed in postcumulus plagioclase. The detailed mineralogy, petrology, and chemistry indicate that olivine and plagioclase react to form the alteration products, except for H 2 O, without changes in the bulk composition of the rocks.

Montana↗

USGS1988

Assimilation of granite by basaltic magma at Burnt Lava flow, Medicine Lake volcano, northern California: Decoupling of heat and mass transfer

At Medicine Lake volcano, California, andesite of the Holocene Burnt Lava flow has been produced by fractional crystallization of parental high alumina basalt (HAB) accompanied by assimilation of granitic crustal material. Burnt Lava contains inclusions of quenched HAB liquid, a potential parent magma of the andesite, highly melted granitic crustal xenoliths, and xenocryst assemblages which provide a record of the fractional crystallization and crustal assimilation process. Samples of granitic crustal material occur as xenoliths in other Holocene and Pleistocene lavas, and these xenoliths are used to constrain geochemical models of the assimilation process. A large amount of assimilation accompanied fractional crystallization to produce the contaminated Burnt lava andesites. Models which assume that assimilation and fractionation occurred simultaneously estimate the ratio of assimilation to fractional crystallization (R) to be >1 and best fits to all geochemical data are at an R value of 1.35 at F=0.68. Petrologic evidence, however, indicates that the assimilation process did not involve continuous addition of granitic crust as fractionation occurred. Instead, heat and mass transfer were separated in space and time. During the assimilation process, HAB magma underwent large amounts of fractional crystallization which was not accompanied by significant amounts of assimilation. This fractionation process supplied heat to melt granitic crust. The models proposed to explain the contamination process involve fractionation, replenishment by parental HAB, and mixing of evolved and parental magmas with melted granitic crust. ?? 1988 Springer-Verlag.

Contributions to Mineralogy and Petrology↗

USGS1985

Strontium and oxygen isotopic variations in Mesozoic and Tertiary plutons of central Idaho

Regional variations in initial 87Sr/86Sr ratios (ri) of Mesozoic plutons in central Idaho locate the edge of Precambrian continental crust at the boundary between the late Paleozoic-Mesozoic accreted terranes and Precambrian sialic crust in western Idaho. The ri values increase abruptly but continuously from less than 0.704 in the accreted terranes to greater than 0.708 across a narrow, 5 to 15 km zone, characterized by elongate, lens-shaped, highly deformed plutons and schistose metasedimentary and metavolcanic units. The chemical and petrologic character of the plutons changes concomitantly from ocean-arc-type, diorite-tonalite-trondhjemite units to a weakly peraluminous, calcic to calcalkalic tonalite-granodiorite-granite suite (the Idaho batholith). Plutons in both suites yield Late Cretaceous ages, but Permian through Early Cretaceous bodies are confined to the accreted terranes and early Tertiary intrusions are restricted to areas underlain by Precambrian crust. The two major terranes were juxtaposed between 75 and 130 m.y. ago, probably between 80 and 95 m.y. Oxygen and strontium isotopic ratios and Rb and Sr concentrations of the plutonic rocks document a significant upper-crustal contribution to the magmas that intrude Precambrian crust. Magmas intruding the arc terranes were derived from the upper mantle/subducted oceanic lithosphere and may have been modified by anatexis of earlier island-arc volcanic and sedimentary units. Plutons near the edge of Precambrian sialic crust represent simple mixtures of the Precambrian wall-rocks with melts derived from the upper mantle or subducted oceanic lithosphere with ri of 0.7035. Rb/Sr varies linearly with ri, producing "pseudoisochrons" with apparent "ages" close to the age of the wall rocks. Measured ??18O values of the wall rocks are less than those required for the assimilated end-member by Sr-O covariation in the plutons, however, indicating that wall-rock ??18O was reduced significantly by exchange with circulating fluids. Metasedimentary rocks of the Belt Supergroup are similarly affected near the batholith, documenting a systematic depletion in 18O as much as 50 km from the margin of the batholith. Plutons of the Bitterroot lobe of the Idaho batholith are remote from the accreted terranes and represent mixtures of Precambrian wall-rocks with melts dominated by continental lower crust (ri>0.708) rather than mantle. "Pseudoisochrons" resulting from these data are actually mixing lines that yield apparent "ages" less than the true age of the wall rocks and meaningless "ri". Assimilation/ fractional-crystallization models permit only insignificant amounts of crystal fractionation during anatexis and mixing for the majority of plutons of the region. ?? 1985 Springer-Verlag.

Contributions to Mineralogy and Petrology↗

USGS2000

Late Holocene hydrous mafic magmatism at the Paint Pot Crater and Callahan flows, Medicine Lake Volcano, N. California and the influence of H2O in the generation of silicic magmas

This paper characterizes late Holocene basalts and basaltic andesites at Medicine Lake volcano that contain high pre-eruptive H 2 O contents inherited from a subduction related hydrous component in the mantle. The basaltic andesite of Paint Pot Crater and the compositionally zoned basaltic to andesitic lavas of the Callahan flow erupted approximately 1000 14 C years Before Present ( 14 C years B . P .). Petrologic, geochemical and isotopic evidence indicates that this late Holocene mafic magmatism was characterized by H 2 O contents of 3 to 6 wt% H 2 O and elevated abundances of large ion lithophile elements (LILE). These hydrous mafic inputs contrast with the preceding episodes of mafic magmatism (from 10,600 to ∼3000 14 C years B . P .) that was characterized by the eruption of primitive high alumina olivine tholeiite (HAOT) with low H 2 O (<0.2 wt%), lower LILE abundance and different isotopic characteristics. Thus, the mantle-derived inputs into the Medicine Lake system have not always been low H 2 O, primitive HAOT, but have alternated between HAOT and hydrous subduction related, calc-alkaline basalt. This influx of hydrous mafic magma coincides temporally and spatially with rhyolite eruption at Glass Mountain and Little Glass Mountain. The rhyolites contain quenched magmatic inclusions similar in character to the mafic lavas at Callahan and Paint Pot Crater. The influence of H 2 O on fractional crystallization of hydrous mafic magma and melting of pre-existing granite crust beneath the volcano combined to produce the rhyolite. Fractionation under hydrous conditions at upper crustal pressures leads to the early crystallization of Fe-Mg silicates and the suppression of plagioclase as an early crystallizing phase. In addition, H 2 O lowers the saturation temperature of Fe and Mg silicates, and brings the temperature of oxide crystallization closer to the liquidus. These combined effects generate SiO 2 -enrichment that leads to rhyodacitic differentiated lavas. In contrast, low H 2 O HAOT magmas at Medicine Lake differentiate to iron-rich basaltic liquids. When these Fe-enriched basalts mix with melted granitic crust, the result is an andesitic magma. Since mid-Holocene time, mafic volcanism has been dominated primarily by hydrous basaltic andesite and andesite at Medicine Lake Volcano. However, during the late Holocene, H 2 O-poor mafic magmas continued to be erupted along with hydrous mafic magmas, although in significantly smaller volumes.

California↗

USGS2016

Tracking the timing of subduction and exhumation using 40 Ar/ 39 Ar phengite ages in blueschist- and eclogite-facies rocks (Sivrihisar, Turkey)

Geochronologic studies of high-pressure/low-temperature rocks can be used to determine the timing and rates of burial and exhumation in subduction zones by dating different stages of the pressure–temperature history. In this study, we present new in situ UV laser ablation 40 Ar/ 39 Ar phengite ages from a suite of lawsonite blueschist- and eclogite-facies rocks representing different protoliths (metabasalt, metasediment), different structural levels (within and outside of a high-strain zone), and different textural positions (eclogite pod core vs. margin) to understand the timing of these events in an exhumed Neo-Tethyan subduction zone (Sivrihisar Massif, Tavşanlı Zone, Turkey). Weighted mean in situ 40 Ar/ 39 Ar ages of phengite from the cores of lawsonite eclogite pods (90–93 Ma) are distinctly older than phengite from retrogressed, epidote eclogite (82 ± 2 Ma). These ages are interpreted as the age of peak and retrograde metamorphism, respectively. Eclogite records the narrowest range of ages (10–14 m.y.) of any rock type analyzed. Transitional eclogite- and blueschist-facies assemblages and glaucophane-rimmed lawsonite + garnet + phengite veins from eclogite pod margins record a much wider age range of 40 Ar/ 39 Ar ages (~20 m.y.) with weighted mean ages of ~91 Ma. Blueschists and quartzites record more variable 40 Ar/ 39 Ar ages that may in part be related to structural position: samples within a high-strain zone at the tectonic contact of the HP rocks with a meta-ultramafic unit have in situ UV laser ablation 40 Ar/ 39 Ar ages of 84.0 ± 1.3–103.7 ± 3.1 Ma, whereas samples outside this zone range to older ages (84.6 ± 2.4–116.7 ± 2.7 Ma) and record a greater age range (22–38 m.y.). The phengite ages can be correlated with the preservation of HP mineral assemblages and fabrics as well as the effects of deformation. Collectively, these results show that high-spatial resolution UV laser ablation 40 Ar/ 39 Ar phengite data, when considered in a petrologic and structural context, may document prograde (burial) and retrograde (exhumation) stages of subduction metamorphism.

Contributions to Mineralogy and Petrology↗

USGS2018

Timescales of magmatic differentiation from alkali basalt to trachyte within the Harrat Rahat volcanic field, Kingdom of Saudi Arabia

A fundamental goal of igneous petrology is to quantify the duration of time required to produce evolved magmas following influx of basalt into the crust. However, in many cases, complex field relations and/or the presence of a long-lived magmatic system make it difficult to assess how basaltic inputs relate to more evolved magmas, therefore, precluding calculation of meaningful timescales. Here, we present field relations, geochemistry, 40 Ar/ 39 Ar ages, and 36 Cl ages for volcanic rocks from the Harrat Rahat volcanic field, Saudi Arabia. These data document a systematic and repeated temporal progression from alkali basalt to trachyte for the youngest eruptives. From ~ 150 to ~ 17 ka the following eruptive sequence occurred four times: (1) alkali basalt, (2) hawaiite, mugearite, or benmoreite, and (3) trachyte. We interpret each eruptive sequence to result from injection of basalt into the crust, and its subsequent differentiation and eruption of progressively evolved magmas. We use the interval time between successive eruptions within a given sequence to calculate the duration of time required to produce trachyte from alkali basalt. Differentiation from alkali basalt to intermediate compositions (hawaiite, mugearite, benmoreite) took ≤ 2 kyr on average. Differentiation from intermediate compositions to trachyte took a maximum of 6.6 ± 3.5 to 22.5 ± 1.6 kyr. Thus, the total duration of differentiation was ~ 9 to ~ 25 kyr. Timescales presented here are insensitive to processes evoked to drive differentiation because they are based solely on the ages and compositions of eruptive products from a system characterized by a simple, repeated differentiation sequence.

Harrat Rahat volcanic field↗

USGS1997

Magmatic processes that generated the rhyolite of Glass Mountain, Medicine Lake volcano, N. California

Glass Mountain consists of a 1 km 3 , compositionally zoned rhyolite to dacite glass flow containing magmatic inclusions and xenoliths of underlying shallow crust. Mixing of magmas produced by fractional crystallization of andesite and crustal melting generated the rhyolite of Glass Mountain. Melting experiments were carried out on basaltic andesite and andesite magmatic inclusions at 100, 150 and 200 MPa, H 2 O-saturated with oxygen fugacity controlled at the nickel-nickel oxide buffer to provide evidence of the role of fractional crystallization in the origin of the rhyolite of Glass Mountain. Isotopic evidence indicates that the crustal component assimilated at Glass Mountain constitutes at least 55 to 60% of the mass of erupted rhyolite. A large volume of mafic andesite (2 to 2.5 km 3 ) periodically replenished the magma reservoir(s) beneath Glass Mountain, underwent extensive fractional crystallization and provided the heat necessary to melt the crust. The crystalline residues of fractionation as well as residual liquids expelled from the cumulate residues are preserved as magmatic inclusions and indicate that this fractionation process occurred at two distinct depths. The presence and composition of amphibole in magmatic inclusions preserve evidence for crystallization of the andesite at pressures of at least 200 MPa (6 km depth) under near H 2 O-saturated conditions. Mineralogical evidence preserved in olivine-plagioclase and olivine-plagioclase-high-Ca clinopyroxene-bearing magmatic inclusions indicates that crystallization under near H 2 O-saturated conditions also occurred at pressures of 100 MPa (3 km depth) or less. Petrologic, isotopic and geochemical evidence indicate that the andesite underwent fractional crystallization to form the differentiated melts but had no chemical interaction with the melted crustal component. Heat released by the fractionation process was responsible for heating and melting the crust.

California↗

USGS2001

Major, trace element and isotope geochemistry (Sr-Nd-Pb) of interplinian magmas from Mt. Somma-Vesuvius (Southern Italy)

Major, trace element and isotopic (Sr, Nd, Pb) data are reported for representative samples of interplinian (Protohistoric, Ancient Historic and Medieval Formations) activity of Mt. Somma-Vesuvius volcano during the last 3500 years. Tephra and lavas exhibit significant major, trace element and isotopic variations. Integration of these data with those obtained by previous studies on the older Somma suites and on the latest activity, allows to better trace a complete petrological and geochemical evolution of the Mt. Somma-Vesuvius magmatism. Three main groups of rocks are recognized. A first group is older than 12.000 yrs, and includes effusive-explosive activity of Mt. Somma. The second group (8000-2700 yrs B.P.) includes the products emitted by the Ottaviano (8000 yrs. B.P.) and Avellino (3550 yrs B.P.) plinian eruptions and the interplinian activity associated with the Protohistoric Formation. Ancient Historic Formation (79-472 A.D.), Medieval Formation (472-1139 A.D.) and Recent interplinian activity (1631-1944 A.D.) belong to the third group of activity (79-1944 A.D.). The three groups of rocks display distinct positive trends of alkalis vs. silica, which become increasingly steeper with age. In the first group there is an increase in silica and alkalis with time, whereas an opposite tendency is observed in the two younger groups. Systematic variations are also evident among the incompatible (Pb, Zr, Hf, Ta, Th, U, Nb, Rb, Cs, Ba) and compatible elements (Sr, Co, Cr). REE document variable degrees of fractionation, with recent activity displaying higher La/Yb ratios than Medieval and Ancient Historic products with the same degree of evolution. N-MORB normalized multi-element diagrams for interplinian rocks show enrichment in Rb, Th, Nb, Zr and Sm (> *10 N-MORB). Sr isotope ratios are variable, with Protohistoric rocks displaying 87Sr/86Sr= 0.70711-0.70810, Ancient Historic 87Sr/86Sr=0.70665-0.70729, and Medieval 87Sr/86Sr=0.70685-0.70803. Neodymium isotopic compositions in the interplinian rocks show a tendency to become slightly more radiogenic with age, from the Protohistoric (143Nd/144Nd=0.51240-0.51247) to Ancient Historic (143Nd/144Nd=0.51245-0.51251). Medieval interplinian activity (143Nd/144Nd: 0.51250-0.51241) lacks meaningful internal trends. All the interplinian rocks have virtually homogeneous compositions of 207Pb/204Pb and 208Pb/204Pb in acid-leached residues (207Pb/204Pb ???15.633 to 15.687, 208Pb/204Pb ???38.947 to 39.181). Values of 206Pb/204Pb are very distinctive, however, and discriminate among the three interplinian cycles of activity (Protohistoric: 18.929-18.971, Ancient Historic: 19.018-19.088, Medieval: 18.964-19.053). Compositional trends of major, trace element and isotopic compositions clearly demonstrate strong temporal variations of the magma types feeding the Somma-Vesuvius activity. These different trends are unlikely to be related only to low pressure evolutionary processes, and reveal variations of parental melt composition. Geochemical data suggest a three component mixing scheme for the interplinian activity. These involve HIMU-type and DMM-type mantle and Calabrian-type lower crust. Interaction between these components has taken place in the source; however, additional quantitative constraints must be acquired in order to better discriminate between magma characteristics inherited from the sources and those acquired during shallow level evolution.

Mineralogy and Petrology↗

USGS1975

Chemical compositions of Kilauea east-rift lava, 1968–1971

The major element chemical compositions of lava from four eruptions on the east rift zone of Kilauea between August 1968 and October 1971 reflect three petrologic processes: Production of chemically distinct batches of magma in the mantle. Separation of olivine, augite, and plagioclase from liquid during flow in the rift-zone conduits. Mixing of different magmas during ascent to the surface. Chemically none of the four Kilauea east-rift eruptions matches the preceding summit eruption in Halemaumau that ended in July 1968. The Mauna Ulu eruption, May 1969 to October 1971 (the last of flie east-rift eruptions), can be divided into five olivine-controlled and chemically distinct variants. Three of these characterize the first seven months of the eruption and are closest in composition to the 1967–8 Halemaumau eruption. Variants 4 and 5 were erupted later and have compositions that are distinctly different from that of the 1967–8 eruption. Major differences are higher Al 2 O 3 (0·15–0·23 per cent), and lower K 2 O (0·07–0·10 per cent) and TiO 2 (0·12–0·23 per cent) in variants 4 and 5 at the same MgO content. Some lavas from eruptions in August and October 1968 and February 1969, have olivine-controlled magma compositions that are identical to mixtures of Mauna Ulu variants 1–3 and the 1967–8 composition. This observation fits an hypothesis advanced earlier by T. L. Wright and R. S. Fiske that magmas in the central magma chamber become mixed with magmas in the rift zone and can be identified as mixing components of rift eruption magmas before they appear as distinctive magmas in summit eruptions. Lavas representing mixing of olivine-controlled magma with differentiated magma were erupted in October 1968, February 1969, and in May and December 1969. The changes in amount of K 2 O and TiO 2 during the latter part of the 1969–71 Mauna Ulu eruption are the reverse of the overall secular change in composition of Kilauea summit lavas from pre-1750 through 1967–8. The K 2 O and TiO 2 contents of the latest overflows during the 1969–71 Mauna Ulu eruption (April 1971) are comparable to that of lava erupted at Kilauea summit prior to 1750. The changing chemistry of Kilauea magma is found to be of use as a ‘tracer’ in the complex Kilauea conduit system. Application of these data to older lava sequences is difficul because of the complexity of the processes controlling lava composition and the absence of detailed information about the time-space chemical variation during individual eruptions.

Hawaii↗

USGS1996

Evidence for multiple mechanisms of crustal contamination of magma from compositionally zoned plutons and associated ultramafic intrusions of the Alaska Range

Models of continental crustal magmagenesis commonly invoke the interaction of mafic mantle-derived magma and continental crust to explain geochemical and petrologic characteristics of crustal volcanic and plutonic rocks. This interaction and the specific mechanisms of crustal contamination associated with it are poorly understood. An excellent opportunity to study the progressive effects of crustal contamination is offered by the composite plutons of the Alaska Range, a series of nine early Tertiary, multiply intruded, compositionally zoned (Peridotite to granite) plutons. Large initial Sr and Nd isotopic contrasts between the crustal country rock and likely parental magmas allow evaluation of the mechanisms and extents of crustal contamination that accompanied the crystallization of these ultra-mafic through granitic rocks. Three contamination processes are distinguished in these plutons. The most obvious of these is assimilation of crustal country rock concurrent with magmatic fractional crystallization (AFC), as indicated by a general trend toward crustal-like isotopic signatures with increasing differentiation. Second, many ultramafic and mafic rocks have late-stage phenocryst reaction and orthocumulate textures that suggest interaction with felsic melt. These rocks also have variable and enriched isotopic compositions that suggest that this felsic melt was isotopically enriched and probably derived from crustal country rock. Partial melt from the flysch country rock may have reacted with and contaminated these partly crystalline magmas following the precipitation and accumulation of the cumulus phenocrysts but before complete solidification of the magma. This suggests that in magmatic mush (especially of ultramafic composition) crystallizing in continental crust, a second distinct process of crustal contamination may be super imposed on AFC or magma mixing involving the main magma body. Finally, nearly all rocks, including mafic and ultramafic rocks, have ( 87 Sr/ 86 Sr) i that are too high, and ε(T) Nd that are too low, to represent the expected isotopic composition of typical depleted mantle. However, gabbro xenoliths with typical depicted-mantle isotopic compositions are found in the plutons. This situation requires either an additional enriched mantle component to provide the parental magma for these plutons, or some mechanism of crustal contamination of the parent magma that did not cause significant crystallization and differentiation of the magma to more felsic compositions. Thermodynamic modeling indicates that assimilation of alkali-and water-rich partial melt of the metapelite country rock by fractionating, near-liquidus basaltic magma could cause significant contamination while suppressing significant crystallization and differentiation.

Journal of Petrology↗

USGS2001

Garnet granulite xenoliths from the Northern Baltic shield: The underplated lower crust of a palaeoproterozoic large igneous province

Garnet granulite facies xenoliths hosted in Devonian lamprophyres from the Kola Peninsula are interpreted to represent the high-grade metamorphic equivalents of continental flood tholeiites, emplaced into the Baltic Shield Archaean lower crust in early Proterozoic time. Geochronological data and similarities in major and trace element geochemistry suggest that the xenoliths formed during the same plume-related magmatic event that created a widespread Palaeoproterozoic large igneous province (LIP) at 2·4–2·5 Ga. They are, thus, the first samples of the lower crust of a Palaeoproterozoic LIP to be studied in petrological detail. The suite includes mafic granulites (gar + cpx + rutile ± plag ± opx ± phlog ± amph), felsic granulites (plag + gar + cpx + rutile ± qtz ± Kspar ± phlog ± amph) and pyroxenites (± phlog ± amph), but mafic garnet granulites predominate. Although some samples are restites, there is no evidence for a predominance of magmatic cumulates, as is common for Phanerozoic lower-crustal xenolith suites. Metasediments are also absent. Phlogopite and/or amphibole occur in xenoliths of all types and are interpreted to be metasomatic in origin. The K-rich metasomatic event occurred at ∼2·0 Ga, and led to substantial enrichment in Rb, K, LREE/HREE, Th/U, Th/Pb and, to a lesser extent, Nb and Ti. The fluids responsible for this metasomatism were probably derived from a second plume that arrived beneath the region at this time. Evidence for partial melting of mafic crust exists in the presence of migmatitic granulites. The timing of migmatization overlaps that of metasomatism, and it is suggested that migmatization was facilitated by the metasomatism. The metamorphism, metasomatism and migmatization recorded in the Kola granulite xenoliths may be representative of the processes responsible for converting Archaean LIP-generated proto-continents into continental crust.

Elovy Island, Kandalaksha Gulf, Kola Peninsula, Wh↗

USGS2021

Proportions, timing, and re-equilibration progress during the 1959 Summit Eruption of Kīlauea: An example of magma mixing processes operating during OIB petrogenesis

Petrographic and chemical analysis of scoria samples collected during the 1959 Kīlauea summit eruption illustrates the progress of thermal and chemical homogenization of the melts, and the gradual growth and/or re-equilibration of olivine phenocrysts, over the course of the eruption. Glass compositions show that thermal equilibration was largely complete within the span of the eruption, whereas chemical homogenization was a work in progress. The olivine phenocryst population, known to contain conspicuous antecrystic components, is also hybrid within the euhedral population. The bulk of the olivine reached the level of the erupting magma on November 18–19, 1959. Zoning patterns in olivine phenocrysts show that initially unzoned grains developed normal zoning by the end of the eruption. Reverse zoning in relatively Fe-rich olivine phenocrysts (interpreted as cognate to the stored magma) was progressively eliminated from November 21 to December 19, 1959, by diffusive re-equilibration between crystals and melt. Toward the end of the eruption, the only olivine composition in direct contact with the melt was Fo 84–86 , with the original rim compositional heterogeneity gone in 4–5 weeks’ time. Activity in December 1959 differed from that in November, as high fountaining events were more closely spaced and almost all samples were picritic, with bulk MgO ≥16·5 wt%. Three different levels were in play during the 1959 eruption: a deep source for high-MgO melts and forsteritic (Fo 87–89 ) olivines, an intermediate source for the bulk of the stored magma, and a shallower source for the most differentiated magma. This model is consistent with geophysical, petrological and chemical observations. Comparison of the 1959 eruption with results from older explosive deposits suggests that stored and recharge melts and olivine from the deeper parts of Kīlauea’s plumbing are similar in composition to those observed or inferred in the 1959 eruption, so they behave similarly during extrusive and explosive periods alike.

Hawaii↗

USGS2009

Petrogenesis of basaltic volcanic rocks from the Pribilof Islands, Alaska, by melting of metasomatically enriched depleted lithosphere, crystallization differentiation, and magma mixing

The Pribilof Islands, Alaska, are located in the Bering Sea in a continental intraplate setting. In this study we examine the petrology and geochemistry of volcanic rocks from St. Paul (0??54-0??003 Ma) and St. George (2??8-1??4 Ma) Islands, the two largest Pribilof Islands. Rocks from St. George can be divided into three groups: group 1 is a high-MgO, low-SiO. 2 suite composed primarily of basanites; group 2 is a high-MgO, high-SiO 2 suite consisting predominantly of alkali basalts; group 3 is an intermediate- to low-MgO suite that includes plagioclase-phyric subalkali basalts and hawaiites. Major and trace element geochemistry suggests that groups 1 and 2 formed by small-degree partial melting of amphibole-bearing to amphibole-free garnet peridotite. Group 1 rocks were the earliest melts produced from the most hydrous parts of the mantle, as they show the strongest geochemical signature of amphibole in their source. The suite of rocks from St. Paul ranges from 14??4 to 4??2 wt % MgO at relatively constant SiO 2 contents (43??1-47??3 wt %). The most primitive St. Paul rocks are modeled as mixtures between magmas with compositions similar to groups 1 and 2 from St. George Island, which subsequently fractionated olivine, clinopyroxene, and spinel to form more evolved rocks. Plagioclase-phyric group 3 rocks from St. George are modeled as mixtures between an evolved melt similar to the evolved magmas on St. Paul and a fractionated group 2 end-member from St. George. Mantle potential temperatures estimated for primitive basanites and alkali basalts are ???1400??C and are similar to those of mid-ocean ridge basalts (MORB). Similarly, 87 Sr/. 86 Sr and 143 Nd/. 144 Nd values for all rocks are MORB-like, in the range of 0??702704-0??703035 and 0??513026-0??513109, respectively. 208 Pb/. 204 Pb vs 206 Pb/. 204 Pb values lie near the MORB end-member but show a linear trend towards HIMU (high time-integrated 238 U/. 204 Pb). Despite isotopic similarities to MORB, many of the major and trace element characteristics are similar to those of ocean island basalts (OIB), including enrichment in alkalis and incompatible trace elements. These characteristics are interpreted to indicate that their mantle source experienced an ancient melt-removal event that is reflected in depleted radiogenic isotopic compositions and was then re-enriched by metasomatism that elevated incompatible trace element contents, but was too young to produce a time-integrated change in radiogenic isotopic ratios. Evidence suggests that the Pribilof Island basalts did not form in either a plume or a back-arc basin tectonic setting. Rather, they were produced by melting of metasomatically hydrated upper mantle peridotite at relatively low temperatures and were able to erupt at the surface through extensional or transtensional faults that served as conduits for the magmas. ?? The Author 2009. Published by Oxford University Press.

Journal of Petrology↗

USGS2013

Hydrogen isotope investigation of amphibole and glass in dacite magmas erupted in 1980-1986 and 2005 at Mount St. Helens, Washington

In active, shallow, sub-volcanic magma conduits the extent of the dehydrogenation–oxidation reaction in amphibole phenocrysts is controlled by energetic processes that cause crystal lattice damage or conditions that increase hydrogen diffusivity in magmatic phases. Amphibole phenocrysts separated from dacitic volcanic rocks erupted from 1980 to 1986 and in 2005 at Mount St. Helens (MSH) were analyzed for δD, water content and Fe 3 +/Fe 2 +, and fragments of glassy groundmass were analyzed for δD and water content. Changes in amphibole δD values through time are evaluated within the context of carefully observed volcanic eruption behavior and published petrological and geochemical investigations. Driving forces for amphibole dehydrogenation include increase in magma oxygen fugacity, decrease in amphibole hydrogen fugacity, or both. The phenocryst amphibole (δD value c. –57‰ and 2 wt % H 2 O) in the white fallout pumice of the May 18, 1980 plinian eruptive phase is probably little modified during rapid magma ascent up an ∼7 km conduit. Younger volcanic rocks incorporate some shallowly degassed dacitic magma from earlier pulses, based on amphibole phenocryst populations that exhibit varying degrees of dehydrogenation. Pyroclastic rocks from explosive eruptions in June–October 1980 have elevated abundances of mottled amphibole phenocrysts (peaking in some pyroclastic rocks erupted on July 22, 1980), and extensive amphibole dehydrogenation is linked to crystal damage from vesiculation and pyroclastic fountain collapse that increased effective hydrogen diffusion in amphibole. Multiple amphibole δD populations in many 1980 pyroclastic rocks combined with their groundmass characteristics (e.g. mixed pumice textures) support models of shallow mixing prior to, or during, eruption as new, volatile-rich magma pulses blended with more oxidized, degassed magma. Amphibole dehydrogenation is quenched at the top surface of MSH dacite lava lobes, but the diversity in the δD amph populations in original fresh lava flow surfaces may occur from blending magma domains with different ascent histories in the sub-volcanic environment immediately before eruption. Multi-stage open-system magma degassing operated in each parcel of magma rising toward the surface, whereas the magma below ∼7 km was a relatively closed system, at least to the October 1986 eruption based on the large population of minimally dehydrogenated, rim-free amphibole in the lavas. Magma degassing and possibly H isotope exchange with low-δD fluids around the roof zone may have accompanied the ∼1·5 km upward migration of the 1980 magma body. The low-δDamph (c. –188 to –122‰) oxy-amphibole phenocrysts in lava spines extruded in May 2005 reflect dehydrogenation as ascending viscous magma degassed and crystallized, and fractures that admitted oxygen into the hot solidified lava spine interior facilitated additional iron oxidation.

Washington↗

USGS2015

Coupled interactions between volatile activity and Fe oxidation state during arc crustal processes

Arc magmas erupted at the Earth’s surface are commonly more oxidized than those produced at mid-ocean ridges. Possible explanations for this high oxidation state are that the transfer of fluids during the subduction process results in direct oxidation of the sub-arc mantle wedge, or that oxidation is caused by the effect of later crustal processes, including protracted fractionation and degassing of volatile-rich magmas. This study sets out to investigate the effect of disequilibrium crustal processes that may involve coupled changes in H 2 O content and Fe oxidation state, by examining the degassing and hydration of sulphur-free rhyolites. We show that experimentally hydrated melts record strong increases in Fe 3+ /∑Fe with increasing H 2 O concentration as a result of changes in water activity. This is relevant for the passage of H 2 O-undersaturated melts from the deep crust towards shallow crustal storage regions, and raises the possibility that vertical variations in f O 2 might develop within arc crust. Conversely, degassing experiments produce an increase in Fe 3+ /∑Fe with decreasing H 2 O concentration. In this case the oxidation is explained by loss of H 2 as well as H 2 O into bubbles during decompression, consistent with thermodynamic modelling, and is relevant for magmas undergoing shallow degassing en route to the surface. We discuss these results in the context of the possible controls on f O 2 during the generation, storage and ascent of magmas in arc settings, in particular considering the timescales of equilibration relative to observation as this affects the quality of the petrological record of magmatic f O 2 .

Journal of Petrology↗

USGS2016

Probing the volcanic-plutonic connection and the genesis of crystal-rich rhyolite in a deeply dissected supervolcano in the Nevada Great Basin: Source of the late Eocene Caetano Tuff

Late Cenozoic faulting and large-magnitude extension in the Great Basin of the western USA has created locally deep windows into the upper crust, permitting direct study of volcanic and plutonic rocks within individual calderas. The Caetano caldera in north–central Nevada, formed during the mid-Tertiary ignimbrite flare-up, offers one of the best exposed and most complete records of caldera magmatism. Integrating whole-rock geochemistry, mineral chemistry, isotope geochemistry and geochronology with field studies and geologic mapping, we define the petrologic evolution of the magmatic system that sourced the >1100 km 3 Caetano Tuff. The intra-caldera Caetano Tuff is up to ∼5 km thick, composed of crystal-rich (30–45 vol. %), high-silica rhyolite, overlain by a smaller volume of comparably crystal-rich, low-silica rhyolite. It defies classification as either a monotonous intermediate or crystal-poor zoned rhyolite, as commonly ascribed to ignimbrite eruptions. Crystallization modeling based on the observed mineralogy and major and trace element geochemistry demonstrates that the compositional zonation can be explained by liquid–cumulate evolution in the Caetano Tuff magma chamber, with the more evolved lower Caetano Tuff consisting of extracted liquids that continued to crystallize and mix in the upper part of the chamber following segregation from a cumulate-rich, and more heterogeneous, source mush. The latter is represented in the caldera stratigraphy by the less evolved upper Caetano Tuff. Whole-rock major, trace and rare earth element geochemistry, modal mineralogy and mineral chemistry, O, Sr, Nd and Pb isotope geochemistry, sanidine Ar–Ar geochronology, and zircon U–Pb geochronology and trace element geochemistry provide robust evidence that the voluminous caldera intrusions (Carico Lake pluton and Redrock Canyon porphyry) are genetically equivalent to the least evolved Caetano Tuff and formed from magma that remained in the lower chamber after ignimbrite eruption and caldera collapse. Thus, the Caetano Tuff contradicts models for the mutually exclusive origins of voluminous volcanic and plutonic magmas in the upper crust. Crystal-scale O isotope data indicate that the Caetano Tuff is one of the most 18 O-enriched rhyolites in the Great Basin (δ 18 O magma = 10·2 ± 0·2‰), supporting anatexis of local metasedimentary basement crust. Metapelite xenoliths in the Carico Lake pluton and ubiquitous xenocrystic zircons in the Caetano Tuff provide constraints for the anatexis process; these data point to shallow (<15 km) dehydration melting of a protolith similar to the Proterozoic McCoy Creek Group siliciclastic sediments in eastern Nevada, projected beneath Caetano in fault-stacked shelf sediments that were thickened during Mesozoic crustal shortening. Mean zircon U–Pb ages for different stratigraphic levels of the intra-caldera Caetano Tuff are 34·2–34·5 Ma, 0·2–0·5 Myr older than the caldera sanidine 40 Ar/ 39 Ar age of 34·00 ± 0·03 Ma, documenting protracted duration of assembly and homogenization of isotopically diverse upper crustal melts, followed by crystallization and zonation to generate the Caetano Tuff magma chamber. Sanidine rims in the least evolved Caetano Tuff and in the Carico Lake pluton and Redrock Canyon porphyry have sharply zoned Ba domains that point to crystal growth during magmatic recharge events. The recharge magma is inferred to have been compositionally similar to the Caetano Tuff magma, with increased Ba resulting from remelting of Ba-rich sanidine cumulates. Mush reactivation to generate the Caetano Tuff eruption was sufficiently rapid to preserve compositional gradients in the intracaldera ignimbrite, calling into question models that predict homogeneity as a prerequisite for remobilizing crystal-rich ignimbrite magmas.

Journal of Petrology↗

USGS2015

Late Pleistocene ages for the most recent volcanism and glacial-pluvial deposits at Big Pine volcanic field, California, USA, from cosmogenic 36 Cl dating

The Big Pine volcanic field is one of several Quaternary volcanic fields that poses a potential volcanic hazard along the tectonically active Owens Valley of east-central California, and whose lavas are interbedded with deposits from Pleistocene glaciations in the Sierra Nevada Range. Previous geochronology indicates an &sim;1.2 Ma history of volcanism, but the eruption ages and distribution of volcanic products associated with the most-recent eruptions have been poorly resolved. To delimit the timing and products of the youngest volcanism, we combine field mapping and cosmogenic 36 Cl dating of basaltic lava flows in the area where lavas with youthful morphology and well-preserved flow structures are concentrated. Field mapping and petrology reveal approximately 15 vents and 6 principal flow units with variable geochemical composition and mineralogy. Cosmogenic 36 Cl exposure ages for lava flow units from the top, middle, and bottom of the volcanic stratigraphy indicate eruptions at &sim;17, 27, and 40 ka, revealing several different and previously unrecognized episodes of late Pleistocene volcanism. Olivine to plagioclase-pyroxene phyric basalt erupted from several vents during the most recent episode of volcanism at &sim;17 ka, and produced a lava flow field covering &sim;35 km 2 . The late Pleistocene 36 Cl exposure ages indicate that moraine and pluvial shoreline deposits that overlie or modify the youngest Big Pine lavas reflect Tioga stage glaciation in the Sierra Nevada and the shore of paleo-Owens Lake during the last glacial cycle.

Geochemistry, Geophysics, Geosystems↗

USGS2016

The role of crystallization-driven exsolution on the sulfur mass balance in volcanic arc magmas

The release of large amounts of sulfur to the stratosphere during explosive eruptions affects the radiative balance in the atmosphere and consequentially impacts climate for up to several years after the event. Quantitative estimations of the processes that control the mass balance of sulfur between melt, crystals, and vapor bubbles is needed to better understand the potential sulfur yield of individual eruption events and the conditions that favor large sulfur outputs to the atmosphere. The processes that control sulfur partitioning in magmas are (1) exsolution of volatiles (dominantly H 2 O) during decompression (first boiling) and during isobaric crystallization (second boiling), (2) the crystallization and breakdown of sulfide or sulfate phases in the magma, and (3) the transport of sulfur-rich vapor (gas influx) from deeper unerupted regions of the magma reservoir. Vapor exsolution and the formation/breakdown of sulfur-rich phases can all be considered as closed-system processes where mass balance arguments are generally easier to constrain, whereas the contribution of sulfur by vapor transport (open system process) is more difficult to quantify. The ubiquitous “excess sulfur” problem, which refers to the much higher sulfur mass released during eruptions than what can be accounted for by amount of sulfur originally dissolved in erupted melt, as estimated from melt inclusion sulfur concentrations (the “petrologic estimate”), reflects the challenges in closing the sulfur mass balance between crystals, melt, and vapor before and during a volcanic eruption. In this work, we try to quantify the relative importance of closed- and open-system processes for silicic arc volcanoes using kinetic models of sulfur partitioning during exsolution. Our calculations show that crystallization-induced exsolution (second boiling) can generate a significant fraction of the excess sulfur observed in crystal-rich arc magmas. This result does not negate the important role of vapor migration in sulfur mass balance but rather points out that second boiling (in situ exsolution) can provide the necessary yield to drive the excess sulfur to the levels observed for crystal-rich systems. In contrast, in crystal-poor systems, magma recharge that releases sulfur-rich bubbles is necessary and most likely the primary contributor to sulfur mass balance. Finally, we apply our model to account for the effect of sulfur partitioning during second boiling and its impact on sulfur released during the Cerro Galan supereruption in Argentina (2.08 Ma) and show the potential importance of second boiling in releasing a large amount of sulfur to the atmosphere during the eruption of large crystal-rich ignimbrites.

Journal of Geophysical Research B: Solid Earth↗