scholarly journals Geochemistry of Basalts from Southwest Indian Ridge 64° E: Implications for the Mantle Heterogeneity East of the Melville Transform

Minerals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 175
Author(s):  
Zhen Dong ◽  
Chunhui Tao ◽  
Jin Liang ◽  
Shili Liao ◽  
Wei Li ◽  
...  
Keyword(s):  
Trace Elements ◽  
Continental Crust ◽  
Major And Trace Elements ◽  
Southwest Indian Ridge ◽  
Spinel Lherzolite ◽  
Lower Continental Crust ◽  
Heavy Rare Earth Elements ◽  
Indian Ridge ◽  
Incompatible Trace Elements ◽  
Ocean Ridge

As one of the regional, magmatic, robust, axial ridge segments along the ultraslow-spreading Southwest Indian Ridge (SWIR), the magmatic process and mantle composition of the axial high relief at 64° E is still unclear. Here, we present major and trace elements and Sr-Nd-Pb isotope data of mid-ocean ridge basalts (MORBs) from 64° E. The basalts show higher contents of Al2O3, SiO2, and Na2O and lower contents of TiO2, CaO, and FeO for a given MgO content, and depletion in heavy rare-earth elements (HREE), enrichment in large-ion lithophile elements, and lower 87Sr/86Sr, 143Nd/144Nd and higher radiogenic Pb isotopes than the depleted MORB mantle (DMM). The high Zr/Nb (24–43) and low Ba/Nb (3.8–7.0) ratios are consistent with typical, normal MORB (N-MORB). Extensive plagioclase fractional crystallization during magma evolution was indicated, while fractionation of olivine and clinopyroxene is not significant, which is consistent with petrographic observations. Incompatible trace elements and isotopic characteristics show that the basaltic melt was formed by the lower partial melting degree of spinel lherzolite than that of segment #27 (i.e., Duanqiao Seamount, 50.5° E), Joseph Mayes Mountain (11.5° E), etc. The samples with a DMM end-member are unevenly mixed with the lower continental crust (LCC)- and the enriched mantle end-member (EM2)-like components, genetically related to the Gondwana breakup and contaminated by upper and lower continental crust (or continental mantle) components.

Petrogenetic insights from chromite in ultramafic cumulates of the Xiarihamu intrusion, northern Tibet Plateau, China

2020 ◽  
Vol 105 (4) ◽  
pp. 479-497 ◽  
Author(s):  
Xie-Yan Song ◽  
Kai-Yuan Wang ◽  
Stephen J. Barnes ◽  
Jun-Nian Yi ◽  
Lie-Meng Chen ◽  
...  
Keyword(s):  
Trace Elements ◽  
Major And Trace Elements ◽  
Tibet Plateau ◽  
Ultramafic Rocks ◽  
Sulfide Deposit ◽  
Northern Tibet ◽  
Mid Ocean Ridge ◽  
Ultramafic Cumulates ◽  
Positive Correlations ◽  
Ocean Ridge

Abstract Chromite is one of the earliest crystallized minerals from mafic melts and has been used as an important “petrogenetic indicator.” Its composition may be modified by interaction with intercumulate melt and adjacent minerals. Thus, chromite in mafic-ultramafic rocks contains clues to the geochemical affinity, evolution, and mantle source of its parent magmas. The Devonian Xiarihamu intrusion, located in the East Kunlun Orogenic Belt in the northern Tibet Plateau, China, hosts a very large disseminated Ni-Co sulfide deposit. This study focuses on geochemistry of the chromite enclosed in olivine of ultramafic rocks of the intrusion. Enrichments in Mg and Al in the rim of the chromite indicate only minor effects of alteration on the compositions of the chromite. The chromites enclosed in the olivines with forsterite percentage (Fo) lower than 87 are characterized by large variations in major and trace elements, such as large ranges of Cr·100/(Cr+Al) (Cr# = 15–47), Mg·100/(Mg+Fe2+) (Mg# = 41–65), and Al2O3 (= 26–53 wt%) as well as 380–3100 ppm V, 70–380 ppm Ga, and 1100–16300 ppm Zn. The chromites display positive correlations between Cr/(Cr+Al) and Ti, Mn, V, Ga, and Sc, inconsistent with fractional crystallization but indicative of an interaction between the chromites, intercumulate melts and hosting minerals. In contrast, chromites hosted in olivine with Fo > 87 in harzburgite have small variations in Cr# (ranging from 37 to 41), Mg# (48 to 51), and Al2O3 (30 to 35 wt%) as well as restricted variation in trace elements, indicating relatively weak interaction with trapped liquid and adjacent phases; these compositions are close to those of the most primitive, earliest crystallized chromites. The most primitive chromite has similarities with chromite in mid-ocean ridge basalt (MORB) in TiO2 and Al2O3 contents (0.19–0.32 and 27.9–36.3 wt%, respectively) and depletion of Sc and enrichment of Ga and Zn relative to MORB chromite. The geochemistry of the chromite indicates a partial melting of the asthenospheric mantle that was modified by melts derived from the subduction slab at garnet-stable pressures.

Trace Element and Isotopic Evidence for Recycled Lithosphere from Basalts from 48 to 53°E, Southwest Indian Ridge

2020 ◽  
Author(s):  
Jixin Wang ◽  
Huaiyang Zhou ◽  
Vincent J M Salters ◽  
Henry J B Dick ◽  
Jared J Standish ◽  
...  
Keyword(s):  
Trace Element ◽  
Southwest Indian Ridge ◽  
Isotopic Compositions ◽  
Depleted Mantle ◽  
Bone Segment ◽  
Mid Ocean Ridge ◽  
Mantle Component ◽  
Indian Ridge ◽  
Basalt Glasses ◽  
Ocean Ridge

Abstract Mantle source heterogeneity and magmatic processes have been widely studied beneath most parts of the Southwest Indian Ridge (SWIR). But less is known from the newly recovered mid-ocean ridge basalts from the Dragon Bone Amagmatic Segment (53°E, SWIR) and the adjacent magmatically robust Dragon Flag Segment. Fresh basalt glasses from the Dragon Bone Segment are clearly more enriched in isotopic composition than the adjacent Dragon Flag basalts, but the trace element ratios of the Dragon Flag basalts are more extreme compared with average mid-ocean ridge basalts (MORB) than the Dragon Bone basalts. Their geochemical differences can be explained only by source differences rather than by variations in degree of melting of a roughly similar source. The Dragon Flag basalts are influenced by an arc-like mantle component as evidenced by enrichment in fluid-mobile over fluid-immobile elements. However, the sub-ridge mantle at the Dragon Flag Segment is depleted in melt component compared with a normal MORB source owing to previous melting in the subarc. This fluid-metasomatized, subarc depleted mantle is entrained beneath the Dragon Flag Segment. In comparison, for the Dragon Bone axial basalts, their Pb isotopic compositions and their slight enrichment in Ba, Nb, Ta, K, La, Sr and Zr and depletion in Pb and Ti concentrations show resemblance to the Ejeda–Bekily dikes of Madagascar. Also, Dragon Bone Sr and Nd isotopic compositions together with the Ce/Pb, La/Nb and La/Th ratios can be modeled by mixing the most isotopically depleted Dragon Flag basalts with a composition within the range of the Ejeda–Bekily dikes. It is therefore proposed that the Dragon Bone axial basalts, similar to the Ejeda–Bekily dikes, are sourced from subcontinental lithospheric Archean mantle beneath Gondwana, pulled from beneath the Madagascar Plateau. The recycling of the residual subarc mantle and the subcontinental lithospheric mantle could be related to either the breakup of Gondwana or the formation and accretion of Neoproterozoic island arc terranes during the collapse of the Mozambique Ocean, and is now present beneath the ridge.

Lateral chemical heterogeneity in the Palaeocene upper mantle beneath the Scottish Hebrides

1980 ◽  
Vol 297 (1431) ◽  
pp. 229-244 ◽  
Keyword(s):  
Trace Elements ◽  
North Atlantic ◽  
Upper Mantle ◽  
Major Element ◽  
Major And Trace Elements ◽  
The North ◽  
Incompatible Elements ◽  
Major Element Chemistry ◽  
Pass Through ◽  
Incompatible Trace Elements

The early major products of Tertiary volcanicity in both Skye and Mull are transitional basic lavas, similar in their major-element chemistry to world-wide alkali basalt series. In contrast, their contents of incompatible trace elements bear more resemblance to those of olivine tholeiites. The Mull basalts have similar ranges of silica saturation, Mg/(Mg+Fe), Y and Yb, but lower overall abundance ranges of strongly incompatible elements than the Skye basalts. The variation of incompatible elements in the Mull and Skye lavas is consistent with a model of a mantle source from which a small amount of melt (no more than 1 % ?) had been extracted, with the pre-Tertiary upper-mantle fusion beneath Mull slightly greater than beneath Skye. Chemical and tectonic considerations suggest that this mantle was neither residual from the formation of the Archaean Lewisian complex, nor emplaced as a result of tension associated with the Gainozoic rifting of the North Atlantic. Data on major and trace elements for a mafic alkalic dyke of the Permian swarms that pass through western Scotland show that these have the requisite geochemical characteristics to have caused this depletion. Such dykes are more abundant in the region of Mull than Skye.

The origin of compositional variation in basalts recovered by submersible drill from Mount Glooscap, Mid-Atlantic Ridge at 36°25′N

1984 ◽  
Vol 21 (8) ◽  
pp. 934-948 ◽  
Author(s):  
James A. Walker ◽  
Patrick J. C. Ryall ◽  
Marcos Zentilli ◽  
Ian L. Gibson ◽  
Jarda Dostal
Keyword(s):  
Trace Elements ◽  
Low Temperature ◽  
Carbonate Rocks ◽  
Compositional Data ◽  
Major And Trace Elements ◽  
Compositional Variation ◽  
Mid Ocean Ridge ◽  
Mid Atlantic Ridge ◽  
Large Peak ◽  
Ocean Ridge

A large peak in the crestal mountains of the Mid-Atlantic Ridge, about 16 km west of the AMAR rift valley at 36°25′N, was sampled for basalt with a submersible electric rock core drill on a comparable surficial scale as the FAMOUS area. Twenty-eight basalt samples from seven drilling stations have been analyzed for major and trace elements. Many of the samples come from flows lying under a cover of carbonate rocks and therefore could not have been sampled by a submersible or a dredge.Through comparisons with published compositional data, it appears that, unlike "FAMOUS-generated" basalts, "AMAR-generated" basalts are, on average, more evolved and are always LREE enriched. Most of the in- and between-hole compositional variation can be accounted for by low-temperature alteration, accumulation of phenocrysts, and low-pressure, relatively low-temperature fractional crystallization. A source heterogeneous in trace elements or undergoing variable degrees of partial melting is necessary to explain the remaining compositional variation. If the large peak can be interpreted as a single volcano, it may be that lavas become progressively more differentiated with time at mid-ocean ridge volcanoes as they commonly do at subduction zone volcanoes.

Tectono-magmatic Interplay and Related Metasomatism in Gabbros of the Chenaillet Ophiolite (Western Alps)

2019 ◽  
Vol 60 (12) ◽  
pp. 2483-2508 ◽  
Author(s):  
R Tribuzio ◽  
G Manatschal ◽  
M R Renna ◽  
L Ottolini ◽  
A Zanetti
Keyword(s):  
Trace Elements ◽  
Trace Element ◽  
Western Alps ◽  
Fine Grained ◽  
Ductile Shearing ◽  
Trace Element Signature ◽  
High Concentrations ◽  
Incompatible Trace Elements ◽  
Detachment Faulting ◽  
Ocean Ridge

Abstract The Jurassic Chenaillet ophiolite in the Western Alps consists of a gabbro–mantle association exhumed to the seafloor through detachment faulting and partly covered by basaltic lavas. One of the Chenaillet gabbroic bodies includes mylonites that are transected by a network of felsic veins, thereby testifying to the interplay of ductile shearing and magma emplacement. The deformed gabbros preserve clinopyroxene porphyroclasts of primary magmatic origin, which are typically mantled by amphibole (titanian edenite) and minor secondary clinopyroxene. Titanian edenite and secondary clinopyroxene also occur as fine-grained syn-kinematic phases locally associated with fine-grained plagioclase. The felsic veins are made up of anorthite-poor plagioclase and minor titanian edenite. Geothermometric investigations document that the ductile gabbro deformation and the crystallization of the felsic veins occurred at 765 ± 50 °C and 800 ± 55 °C, respectively. With respect to undeformed counterparts, the deformed gabbros are variably enriched in SiO2 and variably depleted in Mg/(Mg + Fetot2+) and Ca/(Ca + Na). In addition, the deformed gabbros show relatively high concentrations of incompatible trace elements such as rare earth elements (REE), Y, Zr and Nb. The felsic veins are characterized by low Mg/(Mg + Fetot2+) and Ca/(Ca + Na), high SiO2 and high concentrations of incompatible trace elements. Relict clinopyroxene porphyroclasts from the deformed gabbros display a rather primitive, mid-ocean ridge-type geochemical signature, which contrasts with the trace element fingerprint of titanian edenite from both the deformed gabbros and the felsic veins. For instance, titanian edenite typically has relatively high REE abundances, with chondrite-normalized REE patterns characterized by a pronounced negative Eu anomaly. A similar trace element signature is shown by secondary clinopyroxene from the deformed gabbros. Amphibole from both the deformed gabbros and the felsic veins displays high F/Cl values. We show that the SiO2-rich hydrous melts feeding the felsic veins were involved in the high-temperature gabbro deformation and that melt–gabbro reactions led to major and trace element metasomatism of the deforming gabbros.

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