Partial melting of zoisite eclogite and its significance for trace-element cycling in subduction zones

2006 ◽  
Vol 70 (18) ◽  
pp. A676
Author(s):  
M. Vrabec ◽  
J.C.M. de Hoog ◽  
M. Janak
Author(s):  
Anne-Aziliz Pelleter ◽  
Gaëlle Prouteau ◽  
Bruno Scaillet

Abstract We performed phase equilibrium experiments on a natural Ca-poor pelite at 3 GPa, 750-1000 °C, under moderately oxidizing conditions, simulating the partial melting of such lithologies in subduction zones. Experiments investigated the effect of sulphur addition on phase equilibria and compositions, with S contents of up to ∼ 2.2 wt. %. Run products were characterized for their major and trace element contents, in order to shed light on the role of sulphur on the trace element patterns of melts produced by partial melting of oceanic Ca-poor sediments. Results show that sulphur addition leads to the replacement of phengite by biotite along with the progressive consumption of garnet, which is replaced by an orthopyroxene-kyanite assemblage at the highest sulphur content investigated. All Fe-Mg silicate phases produced with sulphur, including melt, have higher MgO/(MgO+FeO) ratios (relative to S-free/poor conditions), owing to Fe being primarily locked up by sulphide in the investigated redox range. Secular infiltration of the mantle wedge by such MgO and K2O-rich melts may have contributed to the Mg and K-rich character of the modern continental crust. Addition of sulphur does not affect significantly the stability of the main accessory phases controlling the behaviour of trace elements (monazite, rutile and zircon), although our results suggest that monazite solubility is sensitive to S content at the conditions investigated. The low temperature (∼ 800 °C) S-bearing and Ca-poor sediment sourced slab melts show Th and La abundances, Th/La systematics and HFSE signatures in agreement with the characteristics of sediment-rich arc magmas. Because high S contents diminish phengite and garnet stabilities, S-rich and Ca-poor sediment sourced slab melts have higher contents of Rb, B, Li (to a lesser extent), and HREE. The highest ratios of La/Yb are observed in sulphur-poor runs (with a high proportion of garnet, which retains HREE) and beyond the monazite out curve (which retains LREE). Sulphides appear to be relatively Pb-poor and impart high Pb/Ce ratio to coexisting melts, even at high S content. Overall, our results show that Phanerozoic arc magmas from high sediment flux margins owe their geochemical signature to the subduction of terrigenous, sometimes S-rich, sediments. In contrast, subduction of such lithologies during Archean appears unlikely or unrecorded.


2010 ◽  
Vol 74 (2) ◽  
pp. 684-704 ◽  
Author(s):  
Stephan König ◽  
Carsten Münker ◽  
Stephan Schuth ◽  
Ambre Luguet ◽  
J. Elis Hoffmann ◽  
...  

Minerals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 394
Author(s):  
Richen Zhong ◽  
Min Zhang ◽  
Chang Yu ◽  
Hao Cui

A subduction zone plays a critical role in forging continental crust via formation of arc magmas, which are characteristically enriched in large ion lithophile elements (LILEs) and depleted in high field strength elements (HFSEs). This trace element pattern results from the different mobilities of LILEs and HFSEs during slab-to-wedge mass transfer, but the mechanisms of trace element transfer from subducting crusts are not fully understood. In this study, thermodynamic simulations are carried out to evaluate the mobilities of K and Zr, as representative cases of LILE and HFSE, respectively, in slab fluids. The fluids buffered by basaltic eclogite can dissolve > 0.1 molal of K at sub-arc depths (~3 to 5.5 GPa). However, only minor amounts of K can be liberated by direct devolatilization of altered oceanic basalt, because sub-arc dehydration mainly takes place at temperatures < 600 °C (talc-out), wherein the fluid solubility of K is very limited (<0.01 molal). Therefore, serpentinite-derived fluids are required to flush K from the eclogite. The solubility of K can be enhanced by the addition of NaCl to the fluid, because fluid Na+ can unlock phengite-bonded K via a complex ion exchange. Finally, it is further confirmed that Zr and other HFSEs are immobile in slab fluids.


2018 ◽  
Vol 158 (1) ◽  
pp. 143-157 ◽  
Author(s):  
Guangying Feng ◽  
Yildirim Dilek ◽  
Xiaolu Niu ◽  
Fei Liu ◽  
Jingsui Yang

AbstractThe Zhangguangcai Range in the Xing’an Mongolian Orogenic Belt, NE China, contains Early Jurassic (c. 188 Ma) Dabaizigou (DBZG) porphyritic dolerite. Compared with other island-arc mafic rocks, the DBZG dolerite is characterized by high trace-element contents, relatively weak Nb and Ta enrichments, and no Zr, Hf or Ti depletions, similar to OIB-type rocks. Analysed rocks have (87Sr/86Sr)i ratios of 0.7033–0.7044, relatively uniform positive ɛNd(t) values of 2.3–3.2 and positive ɛHf(t) values of 8.5–17.1. Trace-element and isotopic modelling indicates that the DBZG mafic rocks were generated by partial melting of asthenospheric mantle under garnet- to spinel-facies conditions. The occurrence of OIB-like mafic intrusion suggests significant upwelling of the asthenosphere in response to lithospheric attenuation caused by continental rifting. These processes occurred in an incipient continental back-arc environment in the upper plate of a palaeo-Pacific slab subducting W–NW beneath East Asia.


2018 ◽  
Vol 616-617 ◽  
pp. 1066-1076 ◽  
Author(s):  
W. Aaron Wilson ◽  
Andrea K. Fritts ◽  
Mark W. Fritts ◽  
Jason M. Unrine ◽  
Brent N. Tweedy ◽  
...  

2004 ◽  
Vol 22 (5) ◽  
pp. 443-457 ◽  
Author(s):  
F. C. Schröter ◽  
J. A. Stevenson ◽  
N. R. Daczko ◽  
G. L. Clarke ◽  
N. J. Pearson ◽  
...  

Author(s):  
Xiao-Fei Xu ◽  
Long-Long Gou ◽  
Xiao-Ping Long ◽  
Yu-Hang Zhao ◽  
Feng Zhou

Abstract Phase equilibria and trace-element modeling using two previously reported basaltic bulk-rock compositions (samples D11 and 104-16), were carried out in this study, in order to better understand mechanism of low-pressure (LP) partial melting of mafic rocks and associated melt compositions. The T–MH2O pseudosections for both samples at three pressures (i.e. 0.5, 1.0 and 2.0 kbar) display that the H2O-stability field gradually increased with decreasing pressure within the T–MH2O range of 600–1100 °C and 0–12 mol.%. The H2O contents of 10, 5.0, and 0.5 mol.% were selected on the basis of the T–MH2O pseudosections to calculate P–T pseudosections over a P–T window of 0.1–3 kbar and 600–1100 °C, so that the reactions of both the H2O-fluxed and -absent meltings at LP conditions can be investigated. The solidus displays a negative or near-vertical P–T slope, and occurs between 710 and 900 °C at pressure between 0.1 and 3.0 kbar. LP melting of metabasites is attributed to the reactions of the hydrous mineral (hornblende and/or biotite) melting and anhydrous mineral (plagioclase, orthopyroxene, and augite) melting. The hydrous mineral melting is gradually replaced by anhydrous mineral melting as pressure decreasing, as the stability of hornblende decreases with falling pressure. With increasing temperature at a given pressure, the modeled melt compositions are expressed as progressions of the granite-granodiorite-gabbroic diorite fields for sample D11and granite-quartz monzonite-monzonite-gabbroic diorite fields for sample 104-16 on the total alkali–silica diagram. The modeled melts produced through the H2O-fluxed melting display higher Al2O3, CaO, MgO, and lower SiO2 and K2O than those formed by H2O-absent melting at the same P–T conditions. Furthermore, the modeled melts formed by H2O-absent melting, become richer in Al2O3, CaO, MgO, FeO, Na2O, but poorer in SiO2 and K2O as increasing water content. The results of trace-element modeling suggests that the nearly flat REE patterns of modeled bulk-rock composition are inherited by all the modeled melts, and the negative Eu anomalies and Sr depletion of the modeled melts gradually decrease as melting degree increases. Combined with the geochemical characteristics of natural oceanic plagiogranites, which have low K2O contents and flat or slightly LREE-depleted REE patterns, our results imply that a bulk-rock composition with low K2O (&lt;0.17 wt.%) and slightly LREEs depletion is the most likely protolith composition (e.g. basalt D11) for plagiogranites, and the compositions of modeled melts formed by LP H2O-absent partial melting of the basalt D11 at relatively high temperatures (1000–1025 °C) are coincident with those of 1256D tonalites.


Author(s):  
Yue Qi ◽  
Qiang Wang ◽  
Gang-jian Wei ◽  
Xiu-Zheng Zhang ◽  
Wei Dan ◽  
...  

Diverse rock types and contrasting geochemical compositions of post-collisional mafic rocks across the Tibetan Plateau indicate that the underlying enriched lithospheric mantle is heterogeneous; however, how these enriched mantle sources were formed is still debated. The accreted terranes within the Tibetan Plateau experienced multiple stages of evolution. To track the geochemical characteristics of their associated lithospheric mantle through time, we can use mantle-derived magmas to constrain the mechanism of mantle enrichment. We report zircon U-Pb ages, major and trace element contents, and Sr-Nd isotopic compositions for Early Cretaceous and late Eocene mafic rocks in the southern Qiangtang terrane. The Early Cretaceous Baishagang basalts (107.3 Ma) are characterized by low K2O/Na2O (&lt;1.0) ratios, arc-like trace element patterns, and uniform Sr-Nd isotopic compositions [(87Sr/86Sr)i = 0.7067−0.7073, εNd(t) = −0.4 to −0.2]. We suggest that the Baishagang basalts were derived from partial melting of enriched lithospheric mantle that was metasomatized by subducted Bangong−Nujiang oceanic material. We establish the geochemistry of the pre-collisional enriched lithospheric mantle under the southern Qiangtang terrane by combining our data with those from other Early Cretaceous mafic rocks in the region. The late Eocene (ca. 35 Ma) post-collisional rocks in the southern Qiangtang terrane have low K2O/Na2O (&lt;1.0) ratios, and their major element, trace element, and Sr-Nd isotopic compositions [(87Sr/86Sr)i = 0.7042−0.7072, εNd(t) = −4.5 to +1.5] are similar to those of the Early Cretaceous mafic rocks. Based on the distribution, melting depths, and whole-rock geochemical compositions of the Early Cretaceous and late Eocene mafic rocks, we argue that the primitive late Eocene post-collisional rocks were derived from pre-collisional enriched lithospheric mantle, and the evolved samples were produced by assimilation and fractional crystallization of primary basaltic magma. Asthenosphere upwelling in response to the removal of lithospheric mantle induced the partial melting of enriched lithospheric mantle at ca. 35 Ma.


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