Lawsonite geochemistry and stability - implication for trace element and water cycles in subduction zones

2014 ◽  
Vol 32 (5) ◽  
pp. 455-478 ◽  
Author(s):  
L. A. J. Martin ◽  
J. Hermann ◽  
L. Gauthiez-Putallaz ◽  
D. L. Whitney ◽  
A. Vitale Brovarone ◽  
...  
Keyword(s):  
Trace Element ◽  
Subduction Zones ◽  
Water Cycles

scholarly journals The role of sulphur on the melting of Ca-poor sediment and on trace element transfer in subduction zones: an experimental investigation

2021 ◽  
Author(s):  
Anne-Aziliz Pelleter ◽  
Gaëlle Prouteau ◽  
Bruno Scaillet
Keyword(s):  
Trace Element ◽  
Partial Melting ◽  
Subduction Zones ◽  
Sediment Flux ◽  
Arc Magmas ◽  
Trace Element Contents ◽  
The Stability ◽  
Element Transfer ◽  
High Sediment

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.

Boninites as windows into trace element mobility in subduction zones

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

scholarly journals The Fluid Mobilities of K and Zr in Subduction Zones: Thermodynamic Constraints

Minerals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 394
Author(s):  
Richen Zhong ◽  
Min Zhang ◽  
Chang Yu ◽  
Hao Cui
Keyword(s):  
Trace Element ◽  
Subduction Zones ◽  
Critical Role ◽  
High Field Strength ◽  
Trace Element Pattern ◽  
Arc Magmas ◽  
Thermodynamic Simulations ◽  
Element Pattern ◽  
Element Transfer ◽  
Complex Ion

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.

scholarly journals A Crustal Control on the Fe Isotope Systematics of Volcanic Arcs Revealed in Plutonic Xenoliths From the Lesser Antilles

2022 ◽  
Vol 9 ◽  
Author(s):  
G. F. Cooper ◽  
E. C. Inglis
Keyword(s):  
Trace Element ◽  
Mantle Source ◽  
Subduction Zones ◽  
Primary Objective ◽  
Chemical Diversity ◽  
Radiogenic Isotopes ◽  
Lesser Antilles ◽  
Volcanic Arc ◽  
Magmatic Processes ◽  
Isotope Systematics

Lavas produced at subduction zones represent the integration of both source heterogeneity and an array of crustal processes, such as: differentiation; mixing; homogenisation; assimilation. Therefore, unravelling the relative contribution of the sub-arc mantle source versus these crustal processes is difficult when using the amalgamated end products in isolation. In contrast, plutonic xenoliths provide a complementary record of the deeper roots of the magmatic plumbing system and provide a unique record of the true chemical diversity of arc crust. Here, we present the δ56Fe record from well characterised plutonic xenoliths from two distinct volcanic centres in the Lesser Antilles volcanic arc–the islands of Martinique and Statia. The primary objective of this study is to test if the Fe isotope systematics of arc lavas are controlled by sub-arc mantle inputs or during subsequent differentiation processes during a magma’s journey through volcanic arc crust. The Fe isotopic record, coupled to petrology, trace element chemistry and radiogenic isotopes of plutonic xenoliths from the two islands reveal a hidden crustal reservoir of heavy Fe that previously hasn’t been considered. Iron isotopes are decoupled from radiogenic isotopes, suggesting that crustal and/or sediment assimilation does not control the Fe systematics of arc magmas. In contrast to arc lavas, the cumulates from both islands record MORB-like δ56Fe values. In Statia, δ56Fe decreases with major and trace element indicators of differentiation (SiO2, Na2O + K2O, Eu/Eu*, Dy/Yb), consistent with fractionating mineral assemblages along a line of liquid descent. In Martinique, δ56Fe shows no clear relationship with most indicators of differentiation (apart from Dy/Yb), suggesting that the δ56Fe signature of the plutonic xenoliths has been overprinted by later stage processes, such as percolating reactive melts. Together, these data suggest that magmatic processes within the sub-arc crust overprint any source variation of the sub-arc mantle and that a light Fe source is not a requirement to produce the light Fe isotopic compositions recorded in volcanic arc lavas. Therefore, whenever possible, the complimentary plutonic record should be considered in isotopic studies to understand the relative control of the mantle source versus magmatic processes in the crust.

Rapid, paced metamorphism of blueschists from laser-based Lu-Hf garnet-domain geochronology and LA-ICMPS trace element mapping

2021 ◽  
Author(s):  
Lorraine Tual ◽  
Matthijs Smit ◽  
Jamie Cutts ◽  
Ellen Kooijman ◽  
Melanie Kielman-Schmitt ◽  
...  
Keyword(s):  
Trace Element ◽  
Subduction Zone ◽  
Subduction Zones ◽  
Micro Milling ◽  
Individual Growth ◽  
Garnet Growth ◽  
Subduction Zone Processes ◽  
Growth Zones ◽  
Fluid Release ◽  
Element Mapping

&lt;p&gt;Unravelling the timing and rate of subduction-zone metamorphism requires linking the composition of petrogenetic indicator minerals in blueschists and eclogites to time. Garnet is a key mineral in this regard, not in the least because it best records P-T conditions and changes therein and can be dated, using either Lu-Hf or Sm-Nd chronology. Bulk-grain garnet ages are the norm and can provide important and precise time constraints on reactions across both facies. Domain dating, i.e., dating of individual growth zones, moves beyond that. Domain dating by combining mechanical micro-milling and Sm-Nd chronology yielded important constraints on garnet-growth and fluid-release rates for blueschists (e.g., Dragovic et al., 2015). Developing this method for Lu-Hf chronology and, importantly, for &quot;common-sized&quot; garnet (&amp;#8804;1 cm) provides an important opportunity to further explore the potential of this approach.&lt;/p&gt;&lt;p&gt;We combined a low-loss micro-sampling technique in laser cutting with a refined Lu-Hf routine to precisely date multiple growth zones of a sub-cm-sized garnet in a blueschist. The targeted grain from a glaucophane-bearing micaschist from Syros Island, Greece, was chemically characterized by major- and trace-element mapping (EPMA, LA-ICPMS) and five zones were extracted using a laser mill. The three core and inner mantle zones are chemically comparable and identical in age within a 0.1 Myr precision (2&amp;#963;). The outer two zones are chemically distinct and are resolvably younger (0.2-0.8 Myr). The timing of these two major garnet-growth episodes, together with the variations in trace-element chemistry, constrain important fluid-release reactions, such as chloritoid-breakdown. The data show that the integral history of garnet growth in subduction zones may be extremely short (&lt;1 Myr), but may, even in that short timeframe, consist of multiple short pulses. Garnet-forming reactions clearly are localized and, thus, associated with focussed high-flux fluid flow. Beyond subduction-zone processes, our new protocol for zoned garnet Lu-Hf geochronology of &quot;common-sized&quot; garnet opens possibilities for constraining the causes and rates of garnet growth and in turn, the pace of tectonic processes in general.&lt;/p&gt;&lt;p&gt;&amp;#160;&lt;/p&gt;&lt;p&gt;&lt;sub&gt;&lt;em&gt;Dragovic, B., Baxter, E.F. and Caddick, M.J., 2015. Pulsed dehydration and garnet growth during subduction revealed by zoned garnet geochronology and thermodynamic modeling, Sifnos, Greece. Earth and Planetary Science Letters, 413, pp.111-122.&lt;/em&gt;&lt;/sub&gt;&lt;/p&gt;

Oceanic slab-top melting during subduction: Implications for trace-element recycling and adakite petrogenesis

Geology ◽  
2019 ◽  
Vol 48 (3) ◽  
pp. 216-220 ◽  
Author(s):  
David Hernández-Uribe ◽  
Juan David Hernández-Montenegro ◽  
Kim A. Cone ◽  
Richard M. Palin
Keyword(s):  
Trace Element ◽  
Oceanic Crust ◽  
Subduction Zones ◽  
Large Scale ◽  
Thermal Structure ◽  
Experimental Petrology ◽  
Chemical Recycling ◽  
Almost All ◽  
Water Saturated ◽  
Altered Basalt

Abstract Arc volcanism and trace-element recycling are controlled by the devolatilization of oceanic crust during subduction. The type of fluid—either aqueous fluids or hydrous melts—released during subduction is controlled by the thermal structure of the subduction zone. Recent thermomechanical models and results from experimental petrology argue that slab melting occurs in almost all subduction zones, although this is not completely supported by the rock record. Here we show via phase equilibrium modeling that melting of either fresh or hydrothermally altered basalt rarely occurs during subduction, even at water-saturated conditions. Melting occurs only along the hottest slab-top geotherms, with aqueous fluids being released in the forearc region and anatexis restricted to subarc depths, leading to high-SiO2 adakitic magmatism. We posit that aqueous fluids and hydrous melts preferentially enhance chemical recycling in “hot” subduction zones. Our models show that subducted hydrothermally altered basalt is more fertile than pristine basaltic crust, enhancing fluid and melt production during subduction and leading to a greater degree of chemical recycling. In this contribution, we put forward a petrological model to explain (the lack of) melting during the subduction of oceanic crust and suggest that many large-scale models of mass transfer between Earth’s surface and interior may require revision.

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