Investigation into the influence of the Réunion plume on the Central Indian Ridge

Author(s):  
Clément Vincent ◽  
Jung-Woo Park ◽  
Sang-Mook Lee ◽  
Jonguk Kim ◽  
Sang-Joon Pak

<p>Plume-ridge interaction is an important thermal and geological process, which results in various physical and chemical anomalies along a significant length of the global mid-ocean ridge system. Despite numerous studies, some remaining questions to be solved are the origin and mechanisms of geochemical variations and their possible correlation with the morphology of mid-ocean ridges.</p><p>The Central Indian Ridge, with a slow to intermediate spreading rate, provides an ideal opportunity to explore the long-distance plume-ridge interactions. Presently, the ridge is moving away from the Réunion hotspot which is located 1000 km away from the Central Indian Ridge at Réunion Island. Paleogeographic reconstruction suggests that the hotspot crossed the middle part of the Central Indian Ridge (MCIR) between 8°S and 17°S at ~34 Ma. Previous studies argue that the plume material currently flows into the Central Indian Ridge at around 19°S, south of Marie Celeste Fracture Zone (MCFZ) and geochemical enrichments of the mid-ocean ridge basalts (MORB) from the MCIR 14°S and 19°S segments can be attributed to a fossil Réunion plume component. However, a recent geophysical study has suggested that the geochemical anomalies along the Rodrigues segment (18-21°S) can be ascribed to the asthenospheric flow from the Réunion plume, reopening the debate about the origin of the enriched anomalies along the MCIR (14-19°S).</p><p>In this study, we revisited the MCIR from 14°S to 17°S with new geochemical data obtained based on high-resolution sampling and ship-board high-resolution bathymetry data to constrain the influence of the Réunion plume on geochemistry and bathymetry of the MCIR. The results show that trace element ratios and isotopic compositions of on-axis MORB vary in association with ridge discontinuities such as transform faults and non-transform fault discontinuities. The MORB from the northern parts of segments display substantially enriched geochemical features and the enrichments correspond to a shallower axial bathymetry. We attribute the chemical and morphological anomalies along the ridge to the influence of a Réunion plume component focussed by a hotspot leading edge effect. The hotspot leading segments are offset in the direction of the plume and are more efficiently affected by the enriched plume materials. These findings suggest that lithospheric discontinuities such as transform faults and fracture zones may control the flow of mantle plume material into the ridge and the geometry of the ridge coupled to its hotspot proximity may play an important role, particularly in the long-distance plume-ridge interaction.</p>

Lithosphere ◽  
2021 ◽  
Vol 2021 (Special 6) ◽  
Author(s):  
A. Hazra ◽  
A. Saha ◽  
A. Verencar ◽  
M. Satyanarayanan ◽  
S. Ganguly ◽  
...  

Abstract The phenomena of reactive percolation of enriched asthenospheric melts and pervasive melt-rock interactions at mid oceanic ridge-rift systems are the principal proponents for mantle refertilization and compositional heterogeneity. This study presents new mineralogical and geochemical data for the abyssal peridotites exposed along the Vema and Vityaz fracture zones of the Central Indian Ridge (CIR) to address factors contributing to the chemical heterogeneity of CIR mantle. Cr-spinel (Cr#: 0.37-0.59) chemistry classifies these rocks as alpine-type peridotites and corroborates a transitional depleted MORB type to enriched, SSZ-related arc-type magma composition. HFSE and REE geochemistry further attests to an enriched intraoceanic forearc mantle affinity. The distinct boninitic signature of these rocks reflected by LREE>MREE<HREE and PGE compositions substantiates refertilization of the CIR mantle harzburgites by boninitic melt percolation concomitant to initiation of oceanic subduction. The mineral chemistry, trace, and PGE signatures of the CIR peridotites envisage (i) replenishment of depleted sub-ridge upper mantle by impregnation of subduction-derived boninitic melts, (ii) tectonic transition from mid oceanic ridge-rift to an embryonic suprasubduction zone, and (iii) initiation of spontaneous intraoceanic subduction along submarine transform faults and fracture zones of slow-spreading CIR owing to the weakness and mechanical instability of older, denser, and negatively buoyant Indian Ocean lithosphere.


2017 ◽  
Vol 18 (4) ◽  
pp. 1419-1434 ◽  
Author(s):  
Jonguk Kim ◽  
Sang-Joon Pak ◽  
Jai-Woon Moon ◽  
Sang-Mook Lee ◽  
Jihye Oh ◽  
...  

Author(s):  
Hiroshi Sato ◽  
Kentaro Nakamura ◽  
Hidenori Kumagai ◽  
Ryoko Senda ◽  
Tomoaki Morishita ◽  
...  

Geofluids ◽  
2018 ◽  
Vol 2018 ◽  
pp. 1-20 ◽  
Author(s):  
Samuel Pierre ◽  
Alexander P. Gysi ◽  
Thomas Monecke

Seawater-basalt interaction taking place at mid-ocean ridges was studied using numerical modeling to determine the compositional evolution of hydrothermal fluids and associated alteration mineralogy forming within newly emplaced crustal material. Geochemical modeling was carried out in a closed seawater-basalt system at discrete temperature intervals between 2 and 400°C at 500 bars, varying fluid/rock ratios, and secondary mineral assemblages representative of basalt alteration in natural systems. In addition to temperature, the fluid/rock ratio has a fundamental control on the resulting system chemistry. At rock-buffered conditions (low fluid/rock ratios), the mineral-solution equilibrium was characterized by high cation to proton activity ratios foraCa2+/(aH+)2andaNa+/aH+and very low dissolved Mg concentrations due to the precipitation of smectites and chlorite. A complex secondary mineral alteration assemblage dominated by Ca- and Na-bearing minerals including zeolites, calcite, epidote, prehnite, clinozoisite, and albite was predicted to form. The resulting fluid composition was alkaline and reduced relative to ambient seawater, with Eh values ranging between −0.2 and −0.6 V. In contrast, seawater-buffered conditions (high fluid/rock ratios) resulted in lower cation to proton activity ratios foraCa2+/(aH+)2andaNa+/aH+and higher dissolved Mg concentrations comparable to the value of this element in ambient seawater. A more simple mineral assemblage was predicted to form at these conditions with the predominance of Al-Si- and Mg-bearing minerals including kaolinite, quartz, and talc in addition to large amounts of anhydrite. The resulting fluid composition was mildly acidic and oxidized relative to seawater with Eh values ranging between −0.2 and 0 V. These modeling results were compared to a compilation of submarine hydrothermal vent fluid compositions from mid-ocean ridge settings and analogous basalt-dominated environments. The agreement obtained between the simulations and the compiled fluid data indicates that mid-ocean ridge hydrothermal processes can be closely reproduced by mineral-solution equilibria for a broad range of temperatures and fluid/rock ratios.


2020 ◽  
Vol 531 ◽  
pp. 115969 ◽  
Author(s):  
Qing Xiong ◽  
Yong Xu ◽  
José M. González-Jiménez ◽  
Jingao Liu ◽  
Olivier Alard ◽  
...  

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