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  • Articles  (1,361)
  • Oxford University Press  (1,361)
  • Annual Reviews
  • National Academy of Sciences
  • Journal of Petrology  (247)
  • 2319
  • 1
    Publication Date: 2016-06-16
    Description: Large peridotite massifs are scattered along the 1500 km length of the Yarlung–Zangbo Suture Zone (southern Tibet, China), the major suture between Asia and Greater India. Diamonds occur in the peridotites and chromitites of several massifs, together with an extensive suite of trace phases that indicate extremely low f O 2 (SiC, nitrides, carbides, native elements) and/or ultrahigh pressures (UHP) (diamond, TiO 2 II, coesite, possible stishovite). New physical and isotopic (C, N) studies of the diamonds indicate that they are natural, crystallized in a disequilibrium, high- T environment, and spent only a short time at mantle temperatures before exhumation and cooling. These constraints are difficult to reconcile with previous models for the history of the diamond-bearing rocks. Possible evidence for metamorphism in or near the upper part of the Transition Zone includes the following: (1) chromite (in disseminated, nodular and massive chromitites) containing exsolved pyroxenes and coesite, suggesting inversion from a high- P polymorph of chromite; (2) microstructural studies suggesting that the chromitites recrystallized from fine-grained, highly deformed mixtures of wadsleyite and an octahedral polymorph of chromite; (3) a new cubic Mg-silicate, with the space group of ringwoodite but an inverse-spinel structure (all Si in octahedral coordination); (4) harzburgites with coarsely vermicular symplectites of opx + Cr–Al spinel ± cpx; reconstructions suggest that these are the breakdown products of majoritic garnets, with estimated minimum pressures to 〉 13 GPa. Evidence for a shallow pre-metamorphic origin for the chromitites and peridotites includes the following: (1) trace-element data showing that the chromitites are typical of suprasubduction-zone (SSZ) chromitites formed by magma mixing or mingling, consistent with Hf-isotope data from magmatic (375 Ma) zircons in the chromitites; (2) the composition of the new cubic Mg-silicate, which suggests a low- P origin as antigorite, subsequently dehydrated; (3) the peridotites themselves, which carry the trace element signature of metasomatism in an SSZ environment, a signature that must have been imposed before the incorporation of the UHP and low- f O 2 phases. A proposed P – T – t path involves the original formation of chromitites in mantle-wedge harzburgites, subduction of these harzburgites at c . 375 Ma, residence in the upper Transition Zone for 〉200 Myr, and rapid exhumation at c . 170–150 Ma or 130–120 Ma. Os-isotope data suggest that the subducted mantle consisted of previously depleted subcontinental lithosphere, dragged down by a subducting oceanic slab. Thermomechanical modeling shows that roll-back of a (much later) subducting slab would produce a high-velocity channelized upwelling that could exhume the buoyant harzburgites (and their chromitites) from the Transition Zone in 〈 10 Myr. This rapid upwelling, which may explain some characteristics of the diamonds, appears to have brought some massifs to the surface in forearc or back-arc basins, where they provided a basement for oceanic crust. This model can reconcile many apparently contradictory petrological and geological datasets. It also defines an important, previously unrecognized geodynamic process that may have operated along other large suture zones such as the Urals.
    Print ISSN: 0022-3530
    Electronic ISSN: 1460-2415
    Topics: Geosciences
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  • 2
    Publication Date: 2019-08-01
    Description: Ocean island volcanoes erupt a wide range of magmatic compositions via a diverse range of eruptive styles. Understanding where and how these melts evolve is thus an essential component in the anticipation of future volcanic activity. Here we examine the role of crustal structure and magmatic flux in controlling the location, evolution and ultimately composition of melts at Ascension Island. Located in the South Atlantic, Ascension Island is an ocean island volcano that has produced a continuum of eruptive compositions from basalt to rhyolite in its 1 Myr subaerial eruptive history. Volcanic rocks broadly follow a silica-undersaturated subalkaline evolutionary trend, and new data presented here show a continuous compositional trend from basalt through trachyte to rhyolite. Detailed petrographic observations are combined with in situ geochemical analyses of crystals and glass, and new whole-rock major and trace element data from mafic and felsic pyroclastic and effusive deposits that span the entire range in eruptive ages and compositions found on Ascension Island. These data show that extensive fractional crystallization is the main driver for the production of felsic melts for Ascension Island, a volcano built on thin, young, oceanic crust. Strong spatial variations in the compositions of erupted magmas reveal the role of a heterogeneous lower crust; differing degrees of interaction with a zone of plutonic rocks are responsible for the range in mafic lava compositions, and for the formation of the central and eastern felsic complexes. A central core of nested, small-scale plutonic, or mush-like, bodies inhibits the ascent of mafic magmas, allowing sequential fractional crystallization within the lower crust, and generating felsic magmas in the core of the island. There is no evidence for magma mixing preserved in any of the studied eruptions, suggesting that magma storage regions are transient, and material is not recycled between eruptions.
    Print ISSN: 0022-3530
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  • 3
  • 4
    Publication Date: 2013-01-17
    Description: The geochemistry of pyroclasts sampled from four volcanoes along the Kermadec arc in the SW Pacific is used to investigate the genesis of silicic magmas in a young (〈2 Myr), archetypical intra-oceanic arc setting. Raoul, Macauley and Raoul SW volcanoes in the northern Kermadec arc, and Healy volcano in the southern Kermadec arc have all recently erupted dacitic to rhyolitic crystal-poor pumice. In addition to whole-rock analyses, we present a detailed study of mineral and glass chemistries to highlight the complex structure of the Kermadec magmatic systems. Major and trace element bulk-rock compositions mostly fall into relatively narrow compositional ranges, forming discrete groups by eruption for Raoul, and varying with relative crystal contents for Healy. In contrast, pumices from Macauley cover a wide range of compositions, between 66 and 72·5 wt % SiO 2 . At all four volcanoes the trace element patterns of pumice are subparallel to both those of previously erupted basalts and/or whole mafic blebs found both as discrete pyroclasts and as inclusions within pumices. Pb and Sr isotopic compositions have limited ranges within single volcanoes, but vary considerably along the arc, being more radiogenic in the southern volcanoes. Distinctive crystal populations and zonation patterns in pumices, mafic blebs and plutonic xenoliths indicate that many crystals did not grow in the evolved magmas, but are instead mixed from other sources including gabbros and hydrothermally altered tonalites. Such open-system mixing is ubiquitous at the four volcanoes. Oxygen isotope compositions of both phenocrysts (silicic origin) and xenocrysts or antecrysts (mafic origin) are typical for mantle-derived melts. Whole-rock, glass and mineral chemistries are consistent with evolved magmas being generated at each volcano through ~70–80% crystal fractionation of a basaltic parent. Our results are not consistent with silicic magma generation via crustal anatexis, as previously suggested for these Kermadec arc volcanoes. Although crystallization is the dominant process driving melt evolution in the Kermadec volcanoes, we show that the magmatic systems are open to contributions from both newly arriving melts and wholly crystalline plutonic bodies. Such processes occur in variable proportions between magma batches, and are largely reflected in small-scale chemical variations between eruption units.
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  • 5
    Publication Date: 2012-06-22
    Description: The Easter Seamount Chain and Nazca Ridge are two of the most conspicuous volcanic features on the Nazca plate. Many questions about their nature and origin have remained unresolved because of a lack of geochronological and geochemical data for large portions of both chains. New 40 Ar– 39 Ar incremental heating age determinations for dredged rocks from volcanoes east of Salas y Gomez Island show that, with very few exceptions, ages increase steadily to the east from 1·4 to 30 Ma, confirming that the two chains are parts of the same hotspot trail and indicating a hotspot location near Salas y Gomez rather than beneath Easter Island some 400 km farther west. Most of the volcanoes appear to have been erupted onto seafloor that was 5–13 Myr old, and no systematic variation in seafloor age at the time of seamount formation is apparent. At about 23 Ma, the formation of the Nazca Ridge ceased and that of the Easter Seamount Chain began, corresponding to a change in the direction of motion of the Nazca plate. Most of the studied rocks are moderately alkalic to transitional basalts. Their geochemical characteristics suggest that they represent relatively small mean amounts of partial melting initiating in garnet-bearing mantle and ending in the spinel facies. Nd–Sr–Pb isotopic compositions are within the range of values previously observed for volcanoes of the Easter Seamount Chain, west of Easter Island; moreover, most of our data cluster in a rather small part of this range [e.g. Nd (t) is between +6·0 and +4·0]. The results indicate that the mantle source has consisted of the same two principal components, a C/FOZO-type component and a high- Nd , incompatible-element-depleted Pacific mid-ocean ridge basalt-source-type component, since at least 30 Ma. The lack of any geochemical gradient along the chain east of Salas y Gomez implies that no systematic change over time has occurred in the proportions of these end-members.
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  • 6
    Publication Date: 2011-12-23
    Description: Growth and regrowth textures, trace element and oxygen isotope compositions, and water content or species have been studied in alkali feldspars from the late Archaean Closepet igneous bodies. Feldspar crystals grew from mixed magmas that are characterized by a high degree of homogenization. The 3D depiction of trace element distribution indicates that the crystallization process was followed by interaction with fluids. The magmatic system involved in feldspar formation shows non-linear dynamics. The interaction with fluids is also deterministic, but in contrast to magmatic crystallization, it shows an increasing persistency in element behaviour. The degree of persistency of the element activities in both processes has been calculated using the Hurst exponent. The recrystallization (regrowth) process induced by fluids proceeded along crystal fractures and cleavages, causing selective enrichment in large ion lithophile elements (light rare earth elements), Pb, Y, and in various water species. It did not change the feldspar oxygen isotope signature. In turn, the incorporation of hydrogen species into feldspar domains reduced Al–O – –Al defect densities in the structure, decreasing their luminescence. Water speciation shows persistent behaviour during heating, the process being reversible at least up to 600°C. Carbonate crystals with a mantle isotope signature are associated with the re-equilibrated feldspar domains. The feldspar compositions, the abundance of water species in them and the refractory nature of the residuum after heating, the unchanged oxygen isotopes and the mantle signature of co-precipitated carbonates testify that the observed recrystallization has taken place at temperatures above 600°C with H 2 O–CO 2 fertile, mantle-derived fluids. The paper draws special attention to some methodological aspects of the problem. The multi-method approach used here (major element, trace element and isotope geochemistry, infra-red, cathodoluminescence, 3D depiction of geochemical data and fractal statistics) may help to recognize and separate the various processes throughout the alteration history of the pluton.
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  • 7
    Publication Date: 2014-07-17
    Description: New zircon U–Th model-age and trace element datasets are presented from Taupo volcano (New Zealand), which are used to investigate the timescales and broad-scale magmatic processes involving zircon crystallization after the caldera-forming 25·4 ka Oruanui supereruption. Detailed 14 C-based chronologies and controls on vent locations allow the timing and location of post-caldera eruptions to be spatially and temporally constrained to an extent not possible for any other supervolcano. After ~5 kyr of post-Oruanui quiescence, Taupo erupted three dacitic units, followed by another ~5 kyr break, and then a sequence of rhyolitic units in three subgroups (SG1–SG3) from 12 ka onwards. Despite overlapping vent sites and crustal source domains between the Oruanui and post-Oruanui eruptions, U–Th zircon model ages in Taupo SG1 rhyolites (erupted from 12 to 10 ka) indicate only minor inheritance of crystals from the Oruanui magma source. Post-Oruanui model-age spectra are instead typically centred close to eruption ages with subordinate older pre-300 ka equiline grains in some units. U–Pb dating of these older grains shows that both 300–450 ka plutonic-derived and pre-100 Ma greywacke basement-derived zircons are present. The former largely coincide in age with zircons from the 350 ka Whakamaru eruption products, and are dominant over greywacke in young units that were vented within the outline of the Whakamaru caldera. Despite multiple ages and vent sites, trace element compositions are broadly similar in zircons, regardless of their ages. However, a small subset of zircons analysed from SG1 rhyolite (Units B and C) have notably high concentrations of U, Th, P, Y + (REE) 3+ and Nb but with only minor variations in Hf and Ti. SG2 zircons typically have higher Sc contents, reflecting large-scale changes in melt chemistry and crystallizing mineral phases with time. The age spectra indicate that most Oruanui zircons were removed by thermally induced dissolution immediately following the supereruption. U–Th ages from single post-Oruanui eruptions show consistent inheritance of post-Oruanui grains with model ages that centre between the temporally separated but geographically overlapping eruption groups, generating model-age modes. Within the statistical limitations of the isotopic measurements, we interpret these repeated modes to be significant, resulting from incorporation of crystal populations from cyclic post-Oruanui periods of magmatic cooling and crystallization, acting within a crustal protolith chemically independent of that which was dominant in the Oruanui system. These periods of cooling and crystallization alternate with times of rejuvenation and eruption, sometimes demonstrably accompanying syn-eruptive regional rifting and mafic magma injection. Not only were the processes that developed the supersized Oruanui magma body rapid, but this huge magma system was effectively reset and rebuilt on a comparably short timescale.
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