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We investigate the inclusions hosted in peritectic garnet from metapelitic migmatites of the Kinzigite Formation (Ivrea Zone, NW Italy) to evaluate the starting composition of the anatectic melt and fluid regime during anatexis throughout the upper amphibolite facies, transition, and granulite facies zones. Inclusions have negative crystal shapes, sizes from 2 to 10 mu m and are regularly distributed in the core of the garnet. Microstructural and micro-Raman investigations indicate the presence of two types of inclusions: crystallized silicate melt inclusions (i.e., nanogranitoids, NI), and fluid inclusions (FI). Microstructural evidence suggests that FI and NI coexist in the same cluster and are primary (i.e., were trapped simultaneously during garnet growth). FI have similar compositions in the three zones and comprise variable proportions of CO2, CH4, and N-2, commonly with siderite, pyrophyllite, and kaolinite, suggesting a COHN composition of the trapped fluid. The mineral assemblage in the NI contains K-feldspar, plagioclase, quartz, biotite, muscovite, chlorite, graphite and, rarely, calcite. Polymorphs such as kumdykolite, cristobalite, tridymite, and less commonly kokchetavite, were also found. Rehomogenized NI from the different zones show that all the melts are leucogranitic but have slightly different compositions. In samples from the upper amphibolite facies, melts are less mafic (FeO + MgO = 2.0-3.4 wt%), contain 860-1700 ppm CO2 and reach the highest H2O contents (6.5-10 wt%). In the transition zone melts have intermediate H2O (4.8-8.5 wt%), CO2 (457-1534 ppm) and maficity (FeO + MgO = 2.3-3.9 wt%). In contrast, melts at granulite facies reach highest CaO, FeO + MgO (3.2-4.7 wt%), and CO2 (up to 2,400 ppm), with H2O contents comparable (5.4-8.3 wt%) to the other two zones. Our results represent the first clear evidence for carbonic fluid-present melting in the Ivrea Zone. Anatexis of metapelites occurred through muscovite and biotite breakdown melting in the presence of a COH fluid, in a situation of fluid-melt immiscibility. The fluid is assumed to have been internally derived, produced initially by devolatilization of hydrous silicates in the graphitic protolith, then as a result of oxidation of carbon by consumption of Fe3+-bearing biotite during melting. Variations in the compositions of the melts are interpreted to result from higher T of melting. The H2O contents of the melts throughout the three zones are higher than usually assumed for initial H2O contents of anatectic melts. The CO2 contents are highest at granulite facies, and show that carbon-contents of crustal magmas are not negligible at high T. The activity of H2O of the fluid dissolved in granitic melts decreases with increasing metamorphic grade. Carbonic fluid-present melting of the deep continental crust represents, together with hydrate-breakdown melting reactions, an important process in the origin of crustal anatectic granitoids.
Micropetrology
(2018)
Inclusions in minerals, whether fluids, melts or crystalline phases, are small pieces of the large-scale puzzle of Nature, time-consuming to investigate and often of difficult interpretation. Yet they are windows into the past of their host mineral. Mineral inclusions provide the opportunity to unravel the genesis of their host, and the increasingly refined understanding of their elastic behaviour provides the basis for alternative, equilibrium-independent geobarometry. Fluid and melt inclusions reveal information about material transfer in the Earth system, from shallow mineralization to mantle re-fertilization via subduction. The study of inclusions is thus one of the most intriguing and fertile branches of micropetrology. In this contribution, we focus on two recent developments: the use of elasticity models to extract the formation conditions of the host crystal, and the discovery and investigation of melt inclusions in metamorphic rocks. We also discuss how to evaluate the information provided by inclusions, given that they are no longer at the pressure and temperature conditions of entrapment. We discuss how to understand and quantify the changes undergone during cooling and depressurization, and how metastability-related phenomena in inclusions, such as crystallization of rare polymorphs and preservation of the original content of volatiles in fluid and melt inclusions, provide direct evidence that inclusions represent closed systems. The field of study of inclusions in minerals still has a largely untapped potential. The most fruitful avenues for future research will emerge from continuous technological innovation in analytical and imaging techniques, the application of experimental petrology, and the development and application of new theoretical models for coupled mineral behaviour under changing P-T conditions.
In the Pan-African belt of the Dronning Maud Land, Antarctica, crystallized melt inclusions (nanogranitoids) occur in garnet from ultramafic granulites. The granulites contain the peak assemblage pargasite+garnet+clinopyroxene with rare relict orthopyroxene and biotite, and retrograde symplectites at contacts between garnet and amphibole. Garnet contains two generations of melt inclusions. Type 1 inclusions, interpreted as primary, are isolated, < 10 mu m in size, and generally have negative crystal shapes. They contain kokchetavite, kumdykolite, and phlogopite, with quartz and zoisite as minor phases, and undevitrified glass was identified in one inclusion. Type 2 inclusions are < 30 mu m in size, secondary, and contain amphibole, feldspars, and zoisite. Type 2 inclusions appear to be the crystallization products of a melt that coexisted with an immiscible CO2-rich fluid. The nanogranitoids were re-homogenized after heating in a piston-cylinder in a series of four experiments to investigate their composition. The conditions ranged between 900 and 950 degrees C at 1.5-2.4 GPa. Type 1 inclusions are trachytic and ultrapotassic, whereas type 2 melts are dacitic to rhyolitic. Thermodynamic modeling of the ultramafic composition in the MnNCKFMASHTO system shows that anatexis occurred at the end of the prograde P-T path, between the solidus (at ca. 860 degrees C-1.4 GPa) and the peak conditions (at ca. 960 degrees C-1.7 GPa). The model melt composition is felsic and similar to that of type 1 inclusions, particularly when the melting degree is low (< 1 mol%), close to the solidus. However the modeling fails to reproduce the highly potassic signature of the melt and its low H2O content. The combination of petrology, melt inclusion study, and thermodynamic modeling supports the interpretation that melt was produced by anatexis of the ultramafic boudins near peak P-T conditions, and that type 1 inclusions contain the anatectic melt that was present during garnet growth. The felsic, ultrapotassic composition of the primary anatectic melts is compatible with low melting degrees in the presence of biotite and amphibole as reactants.
Three spinel lherzolite xenoliths from Mt. Quincan (Queensland, northeastern Australia) were studied with special attention to their enclosed fluid inclusions. The xenoliths are deformed, have porphyroclastic textures and overall show very similar petrographic features. The only significant difference is manifested in the abundance of fluid inclusions in the samples, mostly in orthopyroxene porphyroclasts. Xenolith JMTQ11 is fluid inclusion-free, whereas xenolith JMTQ20 shows a high abundance of fluid inclusions (fluid inclusion-rich). Xenolith JMTQ45 represents a transitional state between the previous two, as it contains only a small amount of fluid inclusions (fluid inclusion-bearing). Previous studies revealed that these xenoliths and the entrapped fluid inclusions represent a former addition of a MORB-type fluid to the pre-existing lithosphere, resulting from asthenosphere upwelling. There is a progressive enrichment in LREE, Nb, Sr and Ti from the fluid inclusion-free xenolith through the fluid inclusion-bearing one to the fluid inclusion-rich lherzolite. This suggests an increase in the extent of the interaction between the fluid-rich melt and the lherzolite wallrock. In addition, the same interaction is considered to be responsible for the formation of pargasitic amphibole as well. The presence of fluid inclusions indicates fluid migration at mantle depth, and their association with exsolution lamellae in orthopyroxene suggests fluid entrapment following the continental rifting (thermal relaxation) during cooling. A series of analyses, including microthermometry coupled with Raman spectroscopy, FTIR hyperspectral imaging, and Focused Ion Beam-Scanning Electron Microscopy (FIB-SEM) was carried out on the fluid inclusions. Based on the results, the entrapped high-density fluid is composed of 7589 mol% CO2, 918 mol% H2O, 0.11.7 mol% N-2 and <= 0.5 mol% H2S with dissolved trace elements (melt component). Our findings suggest that the metasomatic fluid phase could have been either a fluid/fluid-rich silicate melt released from the deeper asthenosphere, or a coexisting incipient fluid-rich silicate melt. Further cooling, possibly due to thermal relaxation and the upward migration of the fluid phase, caused the investigated lherzolites to reach pargasite stability conditions. We conclude that pargasite, even if only present in very limited modal proportions, can be a common phase at spinel lherzolite stability in the lithospheric upper mantle in continental rift back-arc settings. Studies of fluid inclusions indicate that significant CO2 release from the asthenosphere in a continental rifting environment is resulting from asthenosphere upwelling and its addition to the lithospheric mantle together with fluid-rich melt lherzolite interaction that leaves a CO2-rich fluid behind.
Metamorphic geology
(2019)
Granitic melt inclusions were found in layers of garnet clinopyroxenites from orogenic peridotites hosted in high-pressure felsic granulites of the Granulitgebirge, central Europe. The inclusions are both glassy and crystallized, and occur as clusters in the garnet. Microstructural features suggest that the inclusions formed while garnet was growing as a peritectic phase, likely alongside clinopyroxene. The chemistry of the melt, in particular its trace element signature, shows a crustal contribution, probably due to the involvement of phengite in the melt-producing reaction, most likely in the presence of a fluid. The presence of a granitoid melt in mantle rocks may be the result of localized melting of a phengite-bearing protolith either already present in the peridotites or, more likely, within the local deeply subducted crustal units. In the latter case, the melt would have infiltrated the peridotites and generated pyroxenite via metasomatism. In either case, the presence of granitoid inclusions in orogenic peridotite provides direct evidence for a genetic connection between a high-pressure crustal melt and garnet pyroxenites. The in situ characterization of these remnants of natural melt provides direct quantitative constraints on (one of) the agents responsible for the interaction between crust and mantle.
The global geological volatile cycle (H, C, N) plays an important role in the long term self-regulation of the Earth system. However, the complex interaction between its deep, solid Earth components (i.e. crust and mantle), Earth's fluid envelopes (i.e. atmosphere and hydrosphere) and plate tectonic processes is a subject of ongoing debate. In this study we want to draw attention to how the presence of primary melt (MI) and fluid (FI) inclusions in high-grade metamorphic minerals could help constrain the crustal component of the volatile cycle. To that end, we review the distribution of MI and FI throughout Earth's history, from ca. 3.0 Ga ago up to the present day. We argue that the lower crust might constitute an important, long-term, volatile storage unit, capable to influence the composition of the surface envelopes through the mean of weathering, crustal thickening, partial melting and crustal assimilation during volcanic activity. Combined with thermodynamic modelling, our compilation indicates that periods of well-established plate tectonic regimes at <0.85 Ga and 1.7-2.1 Ga, might be more prone to the reworking of supracrustal lithologies and the storage of volatiles in the lower crust. Such hypothesis has implication beyond the scope of metamorphic petrology as it potentially links geodynamic mechanisms to habitable surface conditions. MI and FI in metamorphic crustal rocks then represent an invaluable archive to assess and quantify the co-joint evolution of plate tectonics and Earth's external processes. (C) 2021 China University of Geosciences (Beijing) and Peking University. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Remnants of hydrous melt formed at mantle depths have been identified and characterized within high-pressure leucogranulites of the Orlica-Snieznik Dome (Bohemian Massif, central Europe). They occur as nanogranites in garnet formed via partial melting of granitoids during the Variscan orogeny. Melt composition and H2O content have been investigated in situ after experimental re-homogenization of the nanogranites, and are consistent with melts produced experimentally from crustal lithologies at mantle depths. This is the first geochemical study of melt inclusions from natural crustal rocks equilibrated close to the stability field of coesite, shedding light on how continental crust melts during deep subduction. Whereas decompressional melting is commonly invoked for deeply subducted crustal lithologies, melting occurred near or at the metamorphic peak pressure in the Orlica-Snieznik granulites. Melting of deeply subducted crustal rocks significantly modifies the rheology and thus promotes fast exhumation: this process has a critical influence on the geodynamic evolution of subduction-collision orogens as well as crustal differentiation at depth.
Garnet brought to the surface by late Miocene granitoids at La Galite Archipelago (Central Mediterranean, Tunisia) contains abundant primary melt and fluid inclusions. Microstructural observations and mineral chemistry define the host garnet as a peritectic phase produced by biotite incongruent melting at ~800 degrees C and 0.5GPa, under fluid-present conditions. The trapped melt is leucogranitic with an unexpected metaluminous and almost peralkaline character. Fluid inclusions are one phase at room temperature, and contain a CO2-dominated fluid, with minor H2O, N-2 and CH4. Siderite and an OH-bearing phase were identified by Raman and IR spectroscopy within every analysed inclusion, and are interpreted as products of a post-entrapment carbonation/hydration reaction between the fluid and the host during cooling. The fluid present during anatexis is therefore inferred to have been originally richer in both H2O and CO2. The production of anatectic melt with a metaluminous signature can be explained as the result of partial melting of relatively Al-poor protoliths assisted by CO2-rich fluids.
With less than two decades of activity, research on melt inclusions (MI) in crystals from rocks that have undergone crustal anatexis - migmatites and granulites - is a recent addition to crustal petrology and geochemistry. Studies on this subject started with glassy inclusions in anatectic crustal enclaves in lavas, and then progressed to regionally metamorphosed and partially melted crustal rocks, where melt inclusions are normally crystallized into a cryptocrystalline aggregate (nanogranitoid).
Since the first paper on melt inclusions in the granulites of the Kerala Khondalite Belt in 2009, reported and studied occurrences are already a few tens. Melt inclusions in migmatites and granulites show many analogies with their more common and long studied counterparts in igneous rocks, but also display very important differences and peculiarities, which are the subject of this review. Microstructurally, melt inclusions in anatectic rocks are small, commonly 10 mu m in diameter, and their main mineral host is peritectic garnet, although several other hosts have been observed. Inclusion contents vary from glass in enclaves that were cooled very rapidly from supersolidus temperatures, to completely crystallized material in slowly cooled regional migmatites. The chemical composition of the inclusions can be analyzed combining several techniques (SEM, EMP, NanoSIMS, LA-ICP-MS), but in the case of crystallized inclusions the experimental remelting under confining pressure in a piston cylinder is a prerequisite. The melt is generally granitic and peraluminous, although granodioritic to trondhjemitic compositions have also been found.
Being mostly primary in origin, inclusions attest for the growth of their peritectic host in the presence of melt. As a consequence, the inclusions have the unique ability of preserving information on the composition of primary anatectic crustal melts, before they undergo any of the common following changes in their way to produce crustal magmas. For these peculiar features, melt inclusions in migmatites and granulites, largely overlooked so far, have the potential to become a fundamental tool for the study of crustal melting, crustal differentiation, and even the generation of the continental crust. (C) 2015 The Authors. Published by Elsevier B.V.