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Geochemistry of continental subduction-zone fluids

dc.contributor.authorZheng, Y.-F.
dc.contributor.authorHermann, Joerg
dc.date.accessioned2015-12-07T22:33:46Z
dc.date.issued2014
dc.date.updated2015-12-07T10:35:21Z
dc.description.abstractThe composition of continental subduction-zone fluids varies dramatically from dilute aqueous solutions at subsolidus conditions to hydrous silicate melts at supersolidus conditions, with variable concentrations of fluid-mobile incompatible trace elements. At ultrahigh-pressure (UHP) metamorphic conditions, supercritical fluids may occur with variable compositions. The water component of these fluids primarily derives from structural hydroxyl and molecular water in hydrous and nominally anhydrous minerals at UHP conditions. While the breakdown of hydrous minerals is the predominant water source for fluid activity in the subduction factory, water released from nominally anhydrous minerals provides an additional water source. These different sources of water may accumulate to induce partial melting of UHP metamorphic rocks on and above their wet solidii. Silica is the dominant solute in the deep fluids, followed by aluminum and alkalis. Trace element abundances are low in metamorphic fluids at subsolidus conditions, but become significantly elevated in anatectic melts at supersolidus conditions. The compositions of dissolved and residual minerals are a function of pressure-temperature and whole-rock composition, which exert a strong control on the trace element signature of liberated fluids. The trace element patterns of migmatic leucosomes in UHP rocks and multiphase solid inclusions in UHP minerals exhibit strong enrichment of large ion lithophile elements (LILE) and moderate enrichment of light rare earth elements (LREE) but depletion of high field strength elements (HFSE) and heavy rare earth elements (HREE), demonstrating their crystallization from anatectic melts of crustal protoliths. Interaction of the anatectic melts with the mantle wedge peridotite leads to modal metasomatism with the generation of new mineral phases as well as cryptic metasomatism that is only manifested by the enrichment of fluid-mobile incompatible trace elements in orogenic peridotites. Partial melting of the metasomatic mantle domains gives rise to a variety of mafic igneous rocks in collisional orogens and their adjacent active continental margins. The study of such metasomatic processes and products is of great importance to understanding of the mass transfer at the slab-mantle interface in subduction channels. Therefore, the property and behavior of subduction-zone fluids are a key for understanding of the crust-mantle interaction at convergent plate margins.
dc.identifier.issn1343-8832
dc.identifier.urihttp://hdl.handle.net/1885/23409
dc.publisherTerra Scientific Publishers
dc.rightsAuthor/s retain copyrighten_AU
dc.sourceEarth, Planets and Space
dc.titleGeochemistry of continental subduction-zone fluids
dc.typeJournal article
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.startpage93
local.contributor.affiliationZheng, Y.-F., University of Science and Technology of China
local.contributor.affiliationHermann, Joerg, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidHermann, Joerg, u9907179
local.description.notesImported from ARIES
local.identifier.absfor040202 - Inorganic Geochemistry
local.identifier.absfor040304 - Igneous and Metamorphic Petrology
local.identifier.absseo970104 - Expanding Knowledge in the Earth Sciences
local.identifier.ariespublicationu8906087xPUB26
local.identifier.citationvolume66
local.identifier.doi10.1186/1880-5981-66-93
local.identifier.scopusID2-s2.0-84908363808
local.identifier.thomsonID000343203700001
local.type.statusPublished Version

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