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  • 1
    In: Earth and planetary science letters, Amsterdam [u.a.] : Elsevier, 1966, 272(2008), 3/4, Seite 541-552, 1385-013X
    In: volume:272
    In: year:2008
    In: number:3/4
    In: pages:541-552
    Beschreibung / Inhaltsverzeichnis: Melt inclusions in olivine are source of unique information about primitive mantle melts. Here we report results of an experimental study aimed at evaluating the ability of olivine to isolate chemically melt inclusions from the host magma after their entrapment. We demonstrate that nearly 'dry' melt inclusions from Galapagos Plateau basalt can gain up to 2.5 wt.% of water if they are placed for 2 days in a water-bearing melt at 200 MPa and 1140 °C. The major element composition of melt inclusions also changed significantly, as a result of a re-equilibration with the olivine host mineral, whereas no significant changes were detected for incompatible trace elements. Our results indicate that inclusions in olivine can rapidly and selectively exchange water with the matrix melt, probably, through combination of proton diffusion and molecular water transport along dislocations in olivine. The fast water transport explains element fractionation, which is not predictable from the theory of magmatic processes. An efficient re-equilibration of melt inclusions with matrix melt can explain the decoupling of water and incompatible trace elements (e.g., H2O vs. K2O) reported for suites of primitive inclusions from mid-ocean-ridge setting and island arcs. Rare cases of well preservation of initial water content in suites of co-genetic inclusions imply very short residence time (a few hours) of the olivine phenocrysts in magma with contrasting water content during fractionation and transport to the surface and rapid quenching upon eruption.
    Materialart: Online-Ressource
    Seiten: Ill., graph. Darst.
    ISSN: 1385-013X
    Sprache: Englisch
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  • 2
    Publikationsdatum: 2023-06-23
    Beschreibung: The Izu–Bonin–Mariana volcanic arc is situated at a convergent plate margin where subduction initiation triggered the formation of MORB-like forearc basalts as a result of decompression melting and near-trench spreading. International Ocean Discovery Program (IODP) Expedition 352 recovered samples within the forearc basalt stratigraphy that contained unusual macroscopic globular textures hosted in andesitic glass (Unit 6, Hole 1440B). It is unclear how these andesites, which are unique in a stratigraphic sequence dominated by forearc basalts, and the globular textures therein may have formed. Here, we present detailed textural evidence, major and trace element analysis, as well as B and Sr isotope compositions, to inves tigate the genesis of these globular andesites. Samples consist of K2 O-rich basaltic globules set in a glassy groundmass of andesitic composition. Between these two textural domains a likely hydrated interface of devitrified glass occurs, which, based on textural evidence, seems to be genetically linked to the formation of the globules. The andesitic groundmass is Cl rich (ca. 3000 𝜇g/g), whereas globules and the interface are Cl poor (ca. 300 𝜇g/g). Concentrations of fluid-mobile trace elements also appear to be fractionated in that globules and show enrichments in B, K, Rb, Cs, and Tl, but not in Ba and W relative to the andesitic groundmass, whereas the interface shows depletions in the latter, but is enriched in the former. Interestingly, globules and andesitic groundmass have identical Sr isotopic composition within analytical uncertainty (87 Sr∕86 Sr of 0.70580 ± 10), indicating that they likely formed from the same source. However, globules show high 𝛿11B (ca. + 7‰), whereas their host andesites are isotopically lighter (ca. – 1 ‰), potentially indicating that whatever process led to their formation either introduced heavier B isotopes to the globules, or induced stable isotope fractionation of B between globules and their groundmass. Based on the bulk of the textural information and geochemical data obtained from these samples, we conclude that these andesites likely formed as a result of the assimilation of shallowly altered oceanic crust (AOC) during forearc basaltic magmatism. Assimilation likely introduced radiogenic Sr, as well as heavier B isotopes to comparatively unradiogenic and low 𝛿11 B forearc basalt parental magmas (average 87 Sr∕86 Sr of 0.703284). Moreover, the globular textures are consistent with their formation being the result of fluid-melt immiscibility that was potentially induced by the rapid release of water from assimilated AOC whose escape likely formed the interface. If the globular textures present in these samples are indeed the result of fluid-melt immiscibility, then this process led to significant trace element and stable isotope fractionation. The textures and chemical compositions of the globules highlight the need for future experimental studies aimed at investigating the exsolution process with respect to potential trace element and isotopic fractionation in arc magmas that have perhaps not been previously considered.
    Beschreibung: Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659
    Beschreibung: Ruhr-Universität Bochum (1007)
    Schlagwort(e): ddc:552.4 ; Izu-Bonin forearc ; Andesites ; Globular textures ; Liquid immiscibility ; B and Sr isotopes
    Sprache: Englisch
    Materialart: doc-type:article
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  • 3
    Publikationsdatum: 2023-06-03
    Beschreibung: Whole rock geochemical analyses of nonfinite suite lavas sampled during IODP Expedition 352 at two sites: U1439C and U1442A. These sites lie in the Izu-Bonin forearc, NE of Chichijima (Bonin Island). The major elements and select trace elements analyzed the X-ray fluorescence spectrometry, other trace elements including the Rare Earth Elements (REE) analyzed by ICP-MS. CO2 was analyzed with a Costech Elemental Analyzer and used to correct major elements for secondary calcite content.
    Schlagwort(e): 352-U1439C; 352-U1442A; Aluminium oxide; Barium; boninite; Calcium oxide; Calculated; Carbon dioxide; CDRILL; Cerium; Chromium; CO2 * 56/44; Cobalt; Code; Core drilling; Corrected for Calcium carbonate; DEPTH, sediment/rock; DSDP/ODP/IODP sample designation; Dysprosium; Element analyser CHN, Costech; Erbium; Europium; Event label; EXP352; Gadolinium; Hafnium; high-Mg andesite; Holmium; IBM; Inductively coupled plasma - mass spectrometry (ICP-MS); Integrated Ocean Drilling Program / International Ocean Discovery Program; IODP; IODP Expedition 352; Iron oxide, Fe2O3; Iron oxide, FeO; Izu-Bonin arc; Izu-Bonin-Mariana fore arc; Joides Resolution; JOIDES Resolution; Lanthanum; Lead; Lithologic unit/sequence; Lutetium; Magnesium/Iron ratio; Magnesium oxide; Main Lithology; Manganese oxide; Neodymium; Nickel; Niobium; Phosphorus; Phosphorus pentoxide; Potassium; Potassium oxide; Praseodymium; Rubidium; Samarium; Sample code/label; Sample comment; Sample ID; Scandium; Silicon dioxide; Sodium oxide; Strontium; Sum; Terbium; Thorium; Thulium; Titanium; Titanium dioxide; Uranium; Vanadium; X-ray fluorescence (XRF); XRF analyses normalized to 100%; Ytterbium; Yttrium; Zirconium
    Materialart: Dataset
    Format: text/tab-separated-values, 4646 data points
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  • 4
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    Unbekannt
    PANGAEA
    In:  Supplement to: Shervais, John W; Reagan, Mark; Haugen, Emily; Almeev, Renat; Pearce, Julian; Prytulak, Julie; Ryan, Jeffrey G; Whattam, Scott Andrew; Godard, Marguerite; Chapman, Timothy; Li, Hongyan; Kurz, Walter; Nelson, Wendy R; Heaton, Daniel; Kirchenbaur, Maria; Shimizu, Kenji; Sakuyama, Tetsuya; Li, Yibing; Vetter, Scott K (2018): Magmatic Response to Subduction Initiation, Part I: Forearc basalts of the Izu-Bonin Arc from IODP Expedition 352. Geochemistry, Geophysics, Geosystems, 19, https://doi.org/10.1029/2018GC007731
    Publikationsdatum: 2023-07-10
    Beschreibung: These basalts represent the earliest response to subduction initiation in the Izu-Bonin arc system during the early Eocene. They are highly refractory and formed by high degrees of partial melting of a previously depleted source.
    Schlagwort(e): 352-U1440A; 352-U1440B; 352-U1441A; Aluminium oxide; Barium; Calcium oxide; Calculated from weight loss after ignition at 450 °C; CDRILL; Cerium; Chromium; Cobalt; Core drilling; DEPTH, sediment/rock; Dysprosium; Erbium; Europium; Event label; Event layer type; EXP352; Gadolinium; Hafnium; Holmium; IBM; ICP-MS; Integrated Ocean Drilling Program / International Ocean Discovery Program; IODP; Iron oxide, Fe2O3; Iron oxide, FeO; Izu-Bonin-Mariana fore arc; Joides Resolution; Lanthanum; Lead; Loss on ignition; Lutetium; Magnesium oxide; Manganese oxide; Mass; Neodymium; Nickel; Niobium; Phosphorus pentoxide; Potassium; Potassium oxide; Praseodymium; Rubidium; Samarium; Sample code/label; Sample ID; Scandium; Silicon dioxide; Sodium oxide; Strontium; Sum; Tantalum; Terbium; Thorium; Thulium; Titanium; Titanium dioxide; Unit; Uranium; Vanadium; X-ray fluorescence (XRF); Ytterbium; Yttrium; Zirconium
    Materialart: Dataset
    Format: text/tab-separated-values, 3494 data points
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  • 5
    Publikationsdatum: 2024-02-02
    Schlagwort(e): Aluminium oxide; Anorthite; Calcium oxide; Calculated, see reference(s); Clinopyroxene; Comment; Degree of fractionation; DERIDGE; Dredge; DRG; Event label; Forsterite; From Mantle to Ocean: Energy-, Material- and Life-cycles at Spreading Axes; Fugacity of oxygen, logarithm; Iron oxide, FeO; M41/2; M41/2_132; M41/2_133; M41/2_136; M41/2_137; M41/2_138; M41/2_139; M41/2_140; M41/2_141; M41/2_142; M41/2_144; M41/2_145; M41/2_146; M41/2_147; M41/2_148; M41/2_149; M41/2_152; M41/2_153; M41/2_154; M41/2_155; M41/2_156; M41/2_158; M41/2_159; M41/2_161; M41/2_162; M41/2_163; M41/2_164; M41/2_166; M41/2_169; M41/2_171; M41/2_172; M41/2_173; M41/2_174; M41/2_188; M41/2_189; M41/2_190; M41/2_191; M41/2_194; M41/2_195; M41/2_198; M41/2_199; M41/2_201; M41/2_202; M41/2_203; Magnesium number; Magnesium oxide; Manganese oxide; Meteor (1986); Method comment; Mid-Atlantic Ridge at 4-11°S; Olivine; Phosphorus pentoxide; Plagioclase; Potassium oxide; Pressure; Sample code/label; Silicon dioxide; Sodium oxide; Temperature, technical; Titanium dioxide; Water in rock
    Materialart: Dataset
    Format: text/tab-separated-values, 1960 data points
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  • 6
    Publikationsdatum: 2024-02-02
    Schlagwort(e): Aluminium oxide; Aluminium oxide, standard deviation; Area/locality; Calcium oxide; Calcium oxide, standard deviation; Calculated; Calculated, see reference(s); Chloride; Chlorine/Potassium ratio; Chromium(III) oxide; Chromium(III) oxide, standard deviation; Comment; DERIDGE; Dredge; DRG; Electron microprobe (EMP); Fourier transform infrared spectroscopy (FTIR); From Mantle to Ocean: Energy-, Material- and Life-cycles at Spreading Axes; Iron oxide, FeO; Iron oxide, FeO, standard deviation; M41/2; M41/2_139; M41/2_140; M41/2_145; M41/2_147; M41/2_149; M41/2_160; M41/2_161; M41/2_164; M41/2_169; M41/2_174; M41/2_190; M41/2_191; Magnesium number; Magnesium oxide; Magnesium oxide, standard deviation; Manganese oxide; Manganese oxide, standard deviation; Meteor (1986); Mid-Atlantic Ridge at 4-11°S; Number; Phosphorus pentoxide; Phosphorus pentoxide, standard deviation; Potassium oxide; Potassium oxide, standard deviation; Sample code/label; Silicon dioxide; Silicon dioxide, standard deviation; Sodium oxide; Sodium oxide, standard deviation; Sum; Titanium dioxide; Titanium dioxide, standard deviation; Water in rock
    Materialart: Dataset
    Format: text/tab-separated-values, 487 data points
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  • 7
    Publikationsdatum: 2024-02-02
    Schlagwort(e): Calculated, see reference(s); Comment; DERIDGE; Dredge; DRG; Event label; From Mantle to Ocean: Energy-, Material- and Life-cycles at Spreading Axes; M41/2; M41/2_132; M41/2_133; M41/2_136; M41/2_137; M41/2_138; M41/2_139; M41/2_140; M41/2_141; M41/2_142; M41/2_143; M41/2_144; M41/2_145; M41/2_146; M41/2_147; M41/2_148; M41/2_149; M41/2_151; M41/2_152; M41/2_153; M41/2_154; M41/2_155; M41/2_157; M41/2_158; M41/2_159; M41/2_160; M41/2_161; M41/2_162; M41/2_163; M41/2_164; M41/2_166; M41/2_167; M41/2_169; M41/2_170; M41/2_171; M41/2_172; M41/2_173; M41/2_174; M41/2_188; M41/2_189; M41/2_190; M41/2_191; M41/2_194; M41/2_195; M41/2_196; M41/2_197; M41/2_198; M41/2_199; M41/2_200; M41/2_201; M41/2_202; M41/2_203; Magnesium number; Meteor (1986); Method comment; Mid-Atlantic Ridge at 4-11°S; Pressure; Sample code/label; Temperature, technical; Water in rock
    Materialart: Dataset
    Format: text/tab-separated-values, 1587 data points
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  • 8
    Publikationsdatum: 2024-02-02
    Beschreibung: Phase equilibria simulations were performed on naturally quenched basaltic glasses to determine crystallization conditions prior to eruption of magmas at the Mid-Atlantic Ridge (MAR) east of Ascension Island (7°11°S).The results indicate that midocean ridge basalt (MORB) magmas beneath different segments of the MAR have crystallized over a wide range of pressures (100-900MPa). However, each segment seems to have a specific crystallization history. Nearly isobaric crystallization conditions (100-300MPa) were obtained for the geochemically enriched MORB magmas of the central segments, whereas normal (N)-MORB magmas of the bounding segments are characterized by polybaric crystallization conditions (200-900MPa). In addition, our results demonstrate close to anhydrous crystallization conditions of N-MORBs, whereas geochemically enriched MORBs were successfully modeled in the presence of 0.4-1wt% H2O in the parental melts.These estimates are in agreement with direct (Fourier transform IR) measurements of H2O abundances in basaltic glasses and melt inclusions for selected samples. Water contents determined in the parental melts are in the range 0.04-0.09 and 0.30-0.55 wt% H2O for depleted and enriched MORBs, respectively. Our results are in general agreement (within ±200MPa) with previous approaches used to evaluate pressure estimates in MORB. However, the determination of pre-eruptive conditions of MORBs, including temperature and water content in addition to pressure, requires the improvement of magma crystallization models to simulate liquid lines of descent in the presence of small amounts of water. KEY WORDS: MORB; Mid-Atlantic Ridge; depth of crystallization; water abundances; phase equilibria calculations; cotectic crystallization; pressure estimates; polybaric fractionation
    Schlagwort(e): DERIDGE; Dredge; DRG; From Mantle to Ocean: Energy-, Material- and Life-cycles at Spreading Axes; M41/2; M41/2_132; M41/2_133; M41/2_136; M41/2_137; M41/2_138; M41/2_139; M41/2_140; M41/2_141; M41/2_142; M41/2_143; M41/2_144; M41/2_145; M41/2_146; M41/2_147; M41/2_148; M41/2_149; M41/2_151; M41/2_152; M41/2_153; M41/2_154; M41/2_155; M41/2_156; M41/2_157; M41/2_158; M41/2_159; M41/2_160; M41/2_161; M41/2_162; M41/2_163; M41/2_164; M41/2_166; M41/2_167; M41/2_169; M41/2_170; M41/2_171; M41/2_172; M41/2_173; M41/2_174; M41/2_188; M41/2_189; M41/2_190; M41/2_191; M41/2_194; M41/2_195; M41/2_196; M41/2_197; M41/2_198; M41/2_199; M41/2_200; M41/2_201; M41/2_202; M41/2_203; Meteor (1986); Mid-Atlantic Ridge at 4-11°S
    Materialart: Dataset
    Format: application/zip, 3 datasets
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  • 9
    Publikationsdatum: 2020-02-06
    Beschreibung: Hydrothermal circulation at slow-spreading ridges is important for cooling the newly formed lithosphere, but the depth to which it occurs is uncertain. Magmas which stagnate and partially crystallize during their rise from the mantle provide a means to constrain the depth of circulation because assimilation of hydrothermal fluids or hydrothermally altered country rock will raise their chlorine (Cl) contents. Here we present Cl concentrations in combination with chemical thermobarometry data on glassy basaltic rocks and melt inclusions from the Southern Mid-Atlantic Ridge (SMAR; ~ 3 cm year−1 full spreading rate) and the Gakkel Ridge (max. 1.5 cm year−1 full spreading rate) in order to define the depth and extent of chlorine contamination. Basaltic glasses show Cl-contents ranging from ca. 50–430 ppm and ca. 40–700 ppm for the SMAR and Gakkel Ridge, respectively, whereas SMAR melt inclusions contain between 20 and 460 ppm Cl. Compared to elements of similar mantle incompatibility (e.g. K, Nb), Cl-excess (Cl/Nb or Cl/K higher than normal mantle values) of up to 250 ppm in glasses and melt inclusions are found in 75% of the samples from both ridges. Cl-excess is interpreted to indicate assimilation of hydrothermal brines (as opposed to bulk altered rock or seawater) based on the large range of Cl/K ratios in samples showing a limited spread in H2O contents. Resorption and disequilibrium textures of olivine, plagioclase and clinopyroxene phenocrysts and an abundance of xenocrysts and gabbroic fragments in the SMAR lavas suggest multiple generations of crystallization and assimilation of hydrothermally altered rocks that contain these brines. Calculated pressures of last equilibration based on the major element compositions of melts cannot provide reliable estimates of the depths at which this crystallization/assimilation occurred as the assimilation negates the assumption of crystallization under equilibrium conditions implicit in such calculations. Clinopyroxene–melt thermobarometry on rare clinopyroxene phenocrysts present in the SMAR magmas yield lower crustal crystallization/assimilation depths (10–13 km in the segment containing clinopyroxene). The Cl-excesses in SMAR melt inclusions indicate that assimilation occurred before crystallization, while also homogeneous Cl in melts from Gakkel Ridge indicate Cl addition during magma chamber processes. Combined, these observations imply that hydrothermal circulation reaches the lower crust at slow-spreading ridges, and thereby promotes cooling of the lower crust. The generally lower Cl-excess at slow-spreading ridges (compared to fast-spreading ridges) is probably related to them having few if any permanent magma chambers. Magmas therefore do not fractionate as extensively in the crust, providing less heat for assimilation (on average, slow-spreading ridge magmas have higher Mg#), and hydrothermal systems are ephemeral, leading to lower total degrees of crustal alteration and more variation in the amount of Cl contamination. Hydrothermal plumes and vent fields have samples in close vicinity that display Cl-excess, mostly of 〉 25 ppm, which thus can aid as a guide for the exploration of (active or extinct) hydrothermal vent fields on the axis.
    Materialart: Article , PeerReviewed
    Format: text
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  • 10
    Publikationsdatum: 2021-02-08
    Beschreibung: Highlights • Cl-rich amphibole (〈1.5 a.p.f.u. Cl) indicates equilibrium with Cl-rich fluid. • Interaction of amphibole with Cl-bearing fluid occurs in rock-dominated environment. • Fluid evolution and changing temperatures recorded in variations in amphibole composition. • Veins and dykelets in lower oceanic crust as signs of hydrothermal alteration. Abstract Hydrothermal veins and dykelets that cross-cut layered olivine gabbros deep in the plutonic section of the Samail Ophiolite, Sultanate of Oman, point towards the occurrence of hydrothermal circulation in the deep oceanic crust, and these features record interactions between rock and high temperature seawater-derived fluids or brines. Deep penetration of seawater-derived fluids down to 100 m above the Moho transition zone and the consequent interactions with the host rock lead to hydrothermal alteration from granulite facies grading down to greenschist facies conditions. Here we present a study of veins and dykelets formed by hydrothermal interaction cutting layered gabbro in the Wadi Wariyah, using petrographic, microanalytical, isotopic, and structural methods. We focus on amphiboles, which show a conspicuous compositional variation from high-Ti magnesiohastingsite and pargasite via magnesiohornblende and edenite, to Cl-rich ferropargasite and hastingsite (up to 1.5 a.p.f.u. Cl) and actinolite. These minerals record a wide range of formation conditions from magmatic to hydrothermal, and reveal a complex history of interactions between rock and hydrothermal fluid or brine in a lower oceanic crustal setting. Large variations in Cl content and cation configurations in amphibole suggest formation in equilibrium with fluids of different salinities at variable fluid/rock ratios. The presence of subsolidus amphibole extremely enriched in chlorine implies phase separation and brine/rock interactions. 87Sr/86Sr values of 0.7031 to 0.7039 and stable δ18O isotopic compositions of 4.1 to 5.6‰ of the different amphibole types suggest a rock-dominated environment, i.e. with low fluid/rock ratios. However, the slight departure from mean Oman isotope values may indicate there was some influence of seawater in the aforementioned fluid-rock interactions. Our study provides new petrological data for the subsolidus evolution of gabbro-hosted amphibole-rich veins in the presence of a seawater-derived fluid.
    Materialart: Article , PeerReviewed
    Format: text
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