Melt Impregnation of Mantle Peridotite Facilitates High‐Temperature Hydration and Mechanical Weakening: Implications for Oceanic Detachment Faults
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Abstract The footwalls of oceanic detachment faults commonly expose shear zone rocks that appear to have compositions intermediate between those of mantle peridotite and magmatic rocks. These compositions either reflect metasomatic mass transfers or they relate to the impregnation of lithospheric mantle with basaltic or more evolved melts. We studied chlorite‐amphibole‐rich shear zone rocks from a detachment fault zone in the 15°20′N Fracture Zone area, Mid‐Atlantic Ridge, to examine their origin and role in strain localization. Geochemical compositions of these rocks imply that they formed by mixing between peridotite and gabbro. Textural observations indicate a strong contrast between the deformation intensity of these hybrid peridotite‐gabbro rocks and the host serpentinized peridotite. Geothermometry data give formation temperatures of >500 °C for synkinematic amphibole, zircon, rutile, and titanite. Chlorite appears intergrown with these phases and likely grew at similar temperatures. These results are compliant to thermodynamic computations that predict comparable mechanically weak mineralogies when hydrating hybrid rocks at 500 to 600 °C, whereas secondary assemblages after pure peridotite or gabbro are considerably stronger. Consequently, metamorphic weakening takes place to a much greater extent in rocks with a hybrid ultramafic–mafic composition than in purely ultramafic or gabbroic lithologies. Deformation may enhance fluid flow, which will in turn increase the extent of hydration and mechanical weakening. A positive feedback loop between hydration and strain localization may hence develop and facilitate the concentration of extensional tectonics into long‐lived, high‐displacement faults. We suggest that hybrid lithologies may play a key role in detachment faulting at slow spreading ridges worldwide.Keywords:
Peridotite
Ultramafic rock
Amphibole
Amphibole
Hornblende
Actinolite
Anorthosite
Tremolite
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Amphibole
Ultramafic rock
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Abstract Amphibole is a common hydrous mineral in mantle rocks. To better understand processes leading to the formation of amphibole‐bearing peridotites and pyroxenites in the lithospheric mantle, we conducted experiments by juxtaposing a lherzolite against hydrous basaltic melts in Au‐Pd capsules. Two melts were examined, a basaltic andesite and a basalt, each containing 4 wt% of water. The experiments were run at 1200°C and 1 GPa for 3 or 12 h, and then cooled to 880°C and 0.8 GPa over 49 h. The reaction at 1200°C produced a melt‐bearing orthopyroxenite‐dunite sequence. Crystallization of the partially reacted melts during cooling lead to the formation of an amphibole‐bearing gabbronorite‐orthopyroxenite‐peridotite sequence. Orthopyroxene in the peridotite and orthopyroxenite has a poikilitic texture enclosing olivines and spinels. Amphibole in the peridotite occurs interstitial to olivine, orthopyroxene, clinopyroxene, and spinel. Comparisons of texture and mineral compositions in the experimental products with those from field observations allow a better understanding of hydrous melt‐rock reaction in the lithospheric mantle. Amphibole‐bearing pyroxenite veins (or dikes) can be formed in the lithospheric mantle or at the crust‐mantle boundary by interaction between hydrous melt and peridotite and subsequent crystallization. Hornblendite or amphibole gabbronorite can be formed in the veins when the flux of hydrous melt is high. Differences in reacting melt and peridotite compositions are responsible for the variation in amphibole composition in mantle xenoliths from different tectonic settings. The extent of melt‐rock reaction is a factor that control amphibole composition across the amphibole‐bearing vein and the host peridotite.
Peridotite
Amphibole
Fractional crystallization (geology)
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We examined vertical variations of the petrological characteristics of a 33-m-thick peridotite section under the layered gabbro section along Wadi Fizh of the northern Oman ophiolite to understand the formation mechanism of the Mohorovicic discontinuity (Moho) beneath a spreading center. Here, we refer to the base of the layered gabbro section as "L-Moho" for the sake of simplicity. Network-like gabbro sills in peridotites increase in frequency upward to the L-Moho. The L-Moho is underlain by a 1-m-thick wehrlite layer, under which exists a 10-m-thick dunite layer, overlying a harzburgite layer where total pyroxenes slightly increase downward. Wehrlite is also found as screens between gabbro layers above the L-Moho. The mineral chemistry indicates systematic variations toward the L-Moho within the peridotite section; the Fo content (91 to 85) and NiO (0.4 to 0.2 wt%) of olivine decrease; the TiO2 content of clinopyroxene (0.1 to 0.6 wt%) and spinel (nil to 1.4 wt%) and atomic ratios of Cr/(Cr + Al) (0.5 to 0.6) and Fe3+/(Cr + Al + Fe3+) (0.05 to >0.1) in spinel increase upsection from the base (harzburgite) to the around L-Moho wehrlite via dunite. These variations are essentially similar to those observed in harzburgite/MORB reaction products from Hess Deep, East Pacific Rise, and possibly indicate that the lithological and mineral chemical variations within the examined peridotite layer resulted from the reaction between a harzburgite and a melt that produced the layered gabbros.
Peridotite
Anorthosite
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Peridotite
Platinum group
Desert (philosophy)
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Amphibole
Layered intrusion
Ultramafic rock
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Amphibole is a common hydrous mineral in mantle rocks. To better understand the processes leading to the formation of amphibole-bearing peridotites and pyroxenites in mantle rocks, we have undertaken an experimental study reacting lherzolite with hydrous basaltic melts in Au-Pd capsules using the reaction couple method. Two melts were examined, a basaltic andesite and a basalt, each containing 4 wt% of water. The experiments were run at 1200°C and 1 GPa for 3 or 12 h, and then cooled to 880°C and 0.8 GPa over 49 h. The reaction at 1200°C and 1 GPa produced a melt-bearing orthopyroxenite-dunite sequence. The cooling stimulates crystallization of orthopyroxene, clinopyroxene, amphibole, and plagioclase, leading to the formation of an amphibole-bearing gabbronorite–orthopyroxenite–peridotite sequence. Compositional variations of minerals in the experiments are controlled by temperature, pressure, and reacting melt composition. Texture, mineralogy, and mineral compositional variation trends obtained from the experiments are similar to those from mantle xenoliths and peridotite massif from the field including amphibole-bearing peridotites and amphibole-bearing pyroxenite and amphibolite that are spatially associated with peridotites, underscoring the importance of hydrous melt-peridotite reaction in the formation of these amphibole-bearing rocks in the upper mantle. Amphiboles in some field samples have distinct textual and mineralogical features and their compositional variation trends are different from that defined by the melt-peridotite reaction experiments. These amphiboles are either crystallized from the host magma that entrained the xenoliths or product of hydrothermal alterations at shallow depths.
Amphibole
Peridotite
Xenolith
Metasomatism
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Peridotite
Amphibole
Xenolith
Maar
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Peridotite
Amphibole
Phlogopite
Solidus
Magnesite
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