Water-assisted migmatization of metagraywackes in a Variscan shear zone, Aiguilles-Rouges massif, western Alps

Migmatitic rocks developed in metagraywackes during the Variscan orogeny in the Aiguilles-Rouges Massif (western Alps). Partial melting took place 320 Ma ago in a 500 m-wide vertical shear zone. Three leucosome types have been recognised on the basis of size and morphology: (1) large leucosomes > 2 cm wide and > 40 cm long lacking mafic selvage, but containing cm-scale mafic enclaves; (2) same as 1 but with thick mafic selvage (melanosome); (3) small leucosomes < 2 cm and < 40 cm) with thin dark selvages (stromatic migmatites). Types 1 + 2 have mineralogical and chemical compositions in keeping with partial melting experiments. But Type 3 leucosomes have identical plagioclase composition (An_19–28) to neighbouring mesosome, both in terms of major- and trace-elements. Moreover, whole-rock REE concentrations in Type 3 leucosomes are only slightly lower than those in the mesosomes, unlike predicted by partial melting experiments. The main chemical differences between all leucosome types can be related to the coupled effect of melt segregation and late chemical reequilibration.

Mineral assemblages and thermodynamic modelling on bulk-rock composition restrict partial melting to  650 °C at 400 MPa. The large volume of leucosome (20 vol.%) thus generated requires addition of 1 wt.% external water. Restriction of extensive migmatization to the shear zone, without melting of neighbouring metapelites, also points to external fluid circulation within the shear zone as the cause of melting.     

Isocon analysis of migmatization in the Front Range, Colorado, USA

Isocon analysis has been applied to five sets of leucosome, mafic selvages and immediately adjacent mesosome in the migmatites from a 15-m outcrop in the Colorado Front Range. The results show: (i) mafic selvages formed from the adjacent mesosome by loss of felsic components and therefore the mesosomes are indeed palaeosomes or protoliths; (ii) the leucosomes did not form in a closed system from the palaeosome (in which case the material lost from the palaeosome during selvage formation would become the leucosome). The observed volumes and compositions of leucosomes require that the present leucosome must contain some material in addition to the felsic components lost from the selvages. The materials that must be added are leucotonalitic to granitic in composition, varying greatly in K/(Na + Ca) ratio. The trend in leucosome composition can be reproduced by assuming that a metasomatic exchange, KNa + Ca, modified originally leucotonalitic leucosomes to more K-rich compositions. These leucosomes most likely formed by injection of silicate melts accompanied, or followed, by metasomatism. The trend of leucosome compositions in this study reflects the general trend in the leucosome compositions which have been published from other areas, indicating that the proposed mechanism can be applicable to other regional migmatites.     

Orthophosphate and biotite chemistry from orthopyroxene-bearing migmatites from California and South India: The role of a fluid-phase in the evolution of granulite-facies migmatites

Migmatites from Cone Peak, California, USA and the Satnur-Sangam road, Southern Karnataka, India contain coarser grained orthopyroxene-bearing leucosomes with subordinate biotite in finer grained hornblende-biotite-pyroxene-bearing hosts. At both localities the leucosomes are enriched in quartz and feldspar and have a higher ratio of pyroxene to hornblende + biotite compared to the host rocks. Biotite grains in leucosomes along the Satnur-Sangam road are concentrated at the margins of orthopyroxene grains and have lower abundances of Ti, Fe, and Cl and a higher abundance of F than biotite grains from the host rock. Fluorapatite grains in all rocks from both localities contain monazite inclusions similar to those produced experimentally by metasomatically induced dissolution and reprecipitation. Some fluorapatite grains at both localities are partially rimmed by allanite. The only compositional differences found between fluorapatite grains in the leucosomes and host rocks were higher concentrations of Cl in grains in leucosomes from Cone Peak. The mineralogies of the rocks suggest that the leucosomes formed by dehydration melting reactions that consumed feldspar, quartz, hornblende, and biotite and produced orthopyroxene. Allanite rims at the margins of fluorapatite grains may have formed by the later retrogression of monazite rims formed by incongruent dissolution of fluorapatite in the melt. Biotite grains at the margins of orthopyroxene crystals in the leucosomes from the Satnur-Sangam road apparently formed by retrogression of orthopyroxene upon the solidification of the anatectic melt. A similar high-grade retrogression did not affect orthopyroxene crystals at Cone Peak, indicating that H₂O was removed from the crystallizing leucosomes probably in a low H₂O activity fluid. Compositional differences between the paleosome and neosomes at Cone Peak are best explained by metasomatic interaction with concentrated brines while elevated Cl concentrations in fluorapatites in the leucosome suggest interaction with a Cl-bearing fluid. Brines may have been responsible for an exchange of elements between the host rock along the Satnur-Sangam road and zones of melt generation now marked by leucosomes, but fluid flow appears to have been less vigorous than at Cone Peak.     

Origin of K-poor leucosomes in a metasedimentary migmatite complex by ultrametamorphism, syn-metamorphic magmatism and subsolidus processes

Two types of stromatic leucosomes are identified in metasedimentary rocks from the Skagit migmatite complex, North Cascades, Washington state, U.S.A. Both types are trondhjemitic and appear similar in outcrop, but, although both contain low abundances of REE, one type consists of leucosomes that are relatively REE-enriched compared to the other, and contains (1) small (<0.8 mm), Fe-rich garnets that are compositionally and texturally different from mesosome and melanosome garnet; (2) Ti-rich minerals (rutile, titanite) that are not present in the groundmass of the associated mesosomes or melanosomes and (3) CO₂-rich fluid inclusions in quartz. Leucosomes of the second type are REE-depleted compared to the first type, lack garnet and Ti-minerals, and contain only H₂O-rich fluid inclusions. The first type of leucosome is interpreted to have formed by in situ partial melting accompanied, and perhaps initiated, by an influx of water-rich fluid during upper amphibolite facies metamorphism. These conclusions are based on estimates of metamorphic P-T-X_fluid conditions (9–10 kbar, > 700°C, water-rich fluid present), inferences about the origin of the above-listed mineralogical and fluid inclusion features, and modeling of leucosome trace element abundances. The second type of leucosome is interpreted to have formed entirely by subsolidus processes (e.g., metamorphic differentiation) because these leucosomes lack features consistent with an origin by partial melting.

K-poor (tonalitic/trondhjemitic) leucosomes associated with metasedimentary (biotite-bearing) source rocks may form by water-saturated partial melting or by subsolidus processes. Both general leucosome-forming mechanisms may operate at different times during upper amphibolite facies regional metamorphism. Partial melting may be initiated by syn-metamorphic magmatic activity if crystallizing plutons serve as external sources of the water-rich fluid necessary for ultrametamorphism in the middle crust during orogenesis. Large-scale migmatite complexes such as the Skagit migmatites may form at least in part in response to contact effects of plutonism associated with high-grade metamorphism, so, although migmatite complexes are a volumetrically substantial part of many orogenic belts, they may not themselves represent a significant original source of magma for larger-scale igneous bodies.     

The Role of Partial Melting and Fractional Crystallization in Determining Discordant Migmatite Leucosome Compositions

Anatectic migmatite leucosomes in the Quetico MetasedimentaryBelt (Superior Province) are discordant to the host rock layering.Two morphological varieties within the anatectic leucosome suiteare distinguished. The first type show little compositionalor textural variation either across, or along, the leucosomes.In contrast, the second variety exhibits both compositionaland textural variations in a single leucosome, typically withinternal cross-cutting relationships. Major-oxide contents varycomparatively little in the Quetico anatectic leucosome suite,but there is a considerable range in the incompatible element(REE, Hf, Zr, Y and Th) concentrations. In particular La contentsrange from 1.8 to 78.1 p.p.m. and the La/Yb ratios from 9.1to 101.9. Samples with high REE contents have negative Eu anomalies,whereas those with low total REE abundances have positive Euanomalies, which indicate that feldspar fractionation was importantin their petrogenesis. Three samples which have no Eu anomalies,and which are taken not to have experienced significant feldsparfractionation, are regarded as the closest approximation toa primary melt composition. Petrographic evidence indicates that only the most aluminousbulk compositions in the host rocks have melted, with cordieriteand biotite as the principal residual phases. Batch partialmelting models indicate that the three leucosomes without Euanomalies could have been derived from 40–80 per centpartial melting of the aluminous metasediments, but garnet musthave been a residual phase. Since the residuum from 40 per centpartial melting is more mafic than any of the rocks currentlyexposed in the area, it is concluded that the melting whichgave rise to the leucosomes occurred at greater depth. Crystallization models indicate that the observed range of leucosomecompositions can be derived by crystal fractionation of meltcompositions similar to the three leucosomes lacking Eu anomalies(i.e. the assumed primary melts). Samples with high abundancesof incompatible elements and negative Eu anomalies representfractionated melts, whereas those with low levels of REE andpositive Eu anomalies represent cumulates. Leucosome composition,morphology and texture can be related to crystallization history,notably the timing of crystallization with respect to leucosomeintrusion. In particular, those leucosomes that exhibit compositionaland textural zoning are interpreted to have undergone crystalfractionation during intrusion. Although a suite of migmatite leucosomes may be derived by partialmelting, it is concluded that the trace-element compositionof any particular leucosome depends, to a great extent, uponits segregation and crystallization history. Indeed, the primarymelt composition may not be preserved.     

Structural,petrological and chemical analysis of syn‐kinematic migmatites: insights from the Western Gneiss Region,Norway

Evidence of melting is presented from the Western Gneiss Region (WGR) in the core of the Caledonian orogen, Western Norway and the dynamic significance of melting for the evolution of orogens is evaluated. Multiphase inclusions in garnet that comprise plagioclase, potassic feldspar and biotite are interpreted to be formed from melt trapped during garnet growth in the eclogite facies. The multiphase inclusions are associated with rocks that preserve macroscopic evidence of melting, such as segregations in mafic rocks, leucosomes and pegmatites hosted in mafic rocks and in gneisses. Based on field studies, these lithologies are found in three structural positions: (i) as zoned segregations found in high‐P (ultra)mafic bodies; (ii) as leucosomes along amphibolite facies foliation and in a variety of discordant structures in gneiss; and (iii) as undeformed pegmatites cutting the main Caledonian structures. Segregations post‐date the eclogite facies foliation and pre‐date the amphibolite facies deformation, whereas leucosomes are contemporaneous with the amphibolite facies deformation, and undeformed pegmatites are post‐kinematic and were formed at the end of the deformation history. The geochemistry of the segregations, leucosomes and pegmatites in the WGR defines two trends, which correlate with the mafic or felsic nature of the host rocks. The first trend with Ca‐poor compositions represents leucosome and pegmatite hosted in felsic gneiss, whereas the second group with K‐poor compositions corresponds to segregation hosted in (ultra)mafic rocks. These trends suggest partial melting of two separate sources: the felsic gneisses and also the included mafic eclogites. The REE patterns of the samples allow distinction between melt compositions, fractionated liquids and cumulates. Melting began at high pressure and affected most lithologies in the WGR before or during their retrogression in the amphibolite facies. During this stage, the presence of melt may have acted as a weakening mechanism that enabled decoupling of the exhuming crust around the peak pressure conditions triggering exhumation of the upward‐buoyant crust. Partial melting of both felsic and mafic sources at temperatures below 800 °C implies the presence of an H₂O‐rich fluid phase at great depth to facilitate H₂O‐present partial melting.     

Insights into the complexity of crustal differentiation: K2O‐poor leucosomes within metasedimentary migmatites from the Southern Marginal Zone of the Limpopo Belt,South Africa

Differentiation of the continental crust is the result of complex interactions between a large number of processes, which govern partial melting of the deep crust, magma formation and segregation, and magma ascent to significantly higher crustal levels. The anatectic metasedimentary rocks exposed in the Southern Marginal Zone of the Limpopo Belt represent an unusually well‐exposed natural laboratory where the portion of these processes that operate in the deep crust can be directly investigated in the field. The formation of these migmatites occurred via absent incongruent melting reactions involving biotite, which produced cm‐ to m‐scale, K₂O‐poor garnet‐bearing stromatic leucosomes, with high Ca/Na ratios relative to their source rocks. Field investigation combined with geochemical analyses, and phase equilibrium modelling designed to investigate some aspects of disequilibrium partial melting show that the outcrop features and compositions of the leucosomes suggest several steps in their evolution: (1) Melting of a portion of the source, with restricted plagioclase availability due to kinetic controls, to produce a magma (melt + entrained peritectic minerals in variable proportions relative to melt); (2) Segregation of the magma at near peak metamorphic conditions into melt accumulation sites (MAS), also known as future leucosome; (3a) Re‐equilibration of the magma with a portion of the bounding mafic residuum via chemical diffusion (H₂O, K₂O), which triggers the co‐precipitation of quartz and plagioclase in the MAS; (3b) Extraction of melt‐dominated magma to higher crustal levels, leaving peritectic minerals entrained from the site of the melting reaction, and the minerals precipitated in the MASs to form the leucosome in the source. The key mechanism controlling this behaviour is the kinetically induced restriction of the amount of plagioclase available to the melting reaction. This results in elevated melt H₂O and K₂O and chemical potential gradient for these components across the leucosome/mafic residuum contact. The combination of all of these processes accurately explains the composition of the K₂O‐poor leucosomes. These findings have important implications for our understanding of melt segregation in the lower crust and minimum melt residency time which, according to the chemical modelling, is <5 years. We demonstrate that in some migmatitic granulites, the leucosomes constitute a type of felsic refractory residuum, rather than evidence of failed magma extraction. This provides a new insight into the ways that source heterogeneity may control anatexis.     

The role of water,mixing processes and metamorphic fabric in the genesis of the Baume migmatites (Ardèche,France)

The Baume migmatites arose from melting of a high-grade metamorphic sequence comprising quartzofeld-spathic and biotite-plagioclase gneisses. Geochemical data and REE modelling suggest that melting occurred under open-system conditions and was caused mainly either by the infiltration along shears of an alkali-rich (K, Rb) aqueous fluid phase or by the injection along foliation planes of granitic magma; some leucosomes result from mixing between in situ partial melts and externally derived granitic materials. Melting appears to be almost independent of the paleosome composition but rather is dependent on the amount of introduced material, itself controlled by the metamorphic fabrics of parent gneisses and/or tectonic structures.     

Melt segregation in the continental crust: distribution and movement of melt in anatectic rocks

The grain‐ and outcrop‐scale distribution of melt has been mapped in anatectic rocks from regional and contact metamorphic environments and used to infer melt movement paths. At the grain scale, anatectic melt is pervasively distributed in the grain boundaries and in small pools; consequently, most melt is located parallel to the principal fabric in the rock, typically a foliation. Short, branched arrays of linked, melt‐bearing grain boundaries connect melt‐depleted parts of the matrix to diffuse zones of melt accumulation (protoleucosomes), where magmatic flow and alignment of euhedral crystals grown from the melt developed. The distribution of melt (leucosome) and residual rocks (normally melanocratic) in outcrop provides different, but complementary, information. The residual rocks show where the melt came from, and the leucosomes preserve some of the channels through which the melt moved, or sites where it pooled. Different stages of the melt segregation process are recorded in the leucosome–melanosome arrays. Regions where melting and segregation had just begun when crystallization occurred are characterized by short arrays of thin, branching leucosomes with little melanosome. A more advanced stage of melting and segregation is marked by the development of residual rocks around extensive, branched leucosome arrays, generally oriented along the foliation or melting layer. Places where melting had stopped, or slowed down, before crystallization began are marked by a high ratio of melanosome to leucosome; because most of the melt has drained away, very few leucosomes remain to mark the melt escape path — this is common in melt‐depleted granulite terranes. Many migmatites contain abundant leucosomes oriented parallel to the foliation; mostly, these represent places where foliation planes dilated and melt drained from the matrix via the branched grain boundary and larger branched melt channel (leucosome) arrays collected. Melt collected in the foliation planes was partially, or fully, expelled later, when discordant leucosomes formed. Leucosomes (or veins) oriented at high angles to the foliation/layering formed last and commonly lack melanocratic borders; hence they were not involved in draining the matrix of the melting layer. Discordant leucosomes represent the channels through which melt flowed out of the melting layer.     

Muscovite dehydration melting in Si-rich metapelites: microstructural evidence from trondhjemitic migmatites,Roded, Southern Israel

Making a distinction between partial melting and subsolidus segregation in amphibolite facies migmatites is difficult. The only significant melting reactions at lowpressures, either vapour saturated or muscovite dehydration melting, do not produce melanocratic peritectic phases. If protoliths are Si-rich and K-poor, then peritectic sillimanite and K-feldspar will form in scarce amounts, and may be lost by retrograde rehydration. The Roded migmatites of southern Israel (northernmost Arabian Nubian Shield) formed at P = 4.5 ± 1 kbar and T ≤ 700 °C and include Si-rich, K-poor paragneissic paleosome and trondhjemitic leucosomes. The lack of K-feldspar in leucosomes was taken as evidence for the non-anatectic origin of the Roded migmatites (Gutkin and Eyal, Isr J Earth Sci 47:117, 1998). It is shown here that although the Roded migmatites experienced significant post-peak deformation and recrystallization, microstructural evidence for partial melting is retained. Based on these microstructures, coupled with pseudosection modelling, indicators of anatexis in retrograded migmatites are established. Phase diagram modelling of neosomes shows the onset of muscovite dehydration melting at 4.5 kbar and 660 °C, forming peritectic sillimanite and K-feldspar. Adjacent non-melted paleosomes lack muscovite and would thus not melt by this reaction. Vapour saturation was not attained, as it would have formed cordierite that does not exist. Furthermore, vapour saturation would not allow peritectic K-feldspar to form, however K-feldspar is ubiquitous in melanosomes. Direct petrographic evidence for anatexis is rare and includes euhedral plagioclase phenocrysts in leucosomes and quartz-filled embayments in corroded plagioclase at leucosome-melanosome interfaces. In deformed and recrystallized rocks muscovite dehydration melting is inferred by: (1) lenticular K-feldspar enclosed by biotite in melanosomes, (2) abundant myrmekite in leucosomes, (3) muscovite–quartz symplectites after sillimanite in melanosomes and associated with myrmekite in leucosomes. While peritectic K-feldspar formed in melanosomes by muscovite dehydration melting reaction, K-feldspar crystallizing from granitic melt in adjacent leucosome was myrmekitized. Excess potassium was used in rehydration of sillimanite to muscovite.     

Origin and evolution of a migmatite

The development of a stromatic migmatite exposed east and southeast of Arvika (Western Sweden) is described in four stages beginning with the country rock and following evolution through three areas characterized by low, medium and high amounts of leucosomes (areas L, M, and H, respectively).The country rock is a paragneiss composed of thin, alternating fine- and coarse-grained layers. Composition of the layers varies from granitic (fine) to tonalitic (coarse layers).The bulk of the stromatic migmatite is composed of leucocratic layers of magmatic appearance (leucosomes) and darker layers of gneissic aspect (mesosomes). Petrographical and chemical data (given in the form of Niggli values and K₂O/SiO₂ diagrams) show a close relationship between the fine-grained paragneiss layers and the leucosomes on the one hand and between the coarse-grained layers and the mesosomes on the other.At relatively low temperatures only those gneiss layers with a suitable (granitic) composition are transformed into leucosomes. This process is interpreted to be due to recrystallization of the felsic minerals via partial melting and to the separation of biotite.With increasing metamorphism, leucosomes become broader and more frequent due to partial melting of layers with less suitable composition. Contacts between different generations of leucosome can be recognized in the form of relict melanosomes.These observations favour essentially isochemical melting, followed by later in-situ crystallization. This model of an isochemical layer-by-layer transformation is supported by the preferential formation of hornblende in leucosomes and relict melanosomes, as well as by almost identical compositions of migmatite and country-rock plagioclase.     

Temporal and compositional differences between subsolidus and anatectic migmatite leucosomes from the Quetico metasedimentary belt, Canada

Abstract Migmatites in the Quetico Metasedimentary Belt contain two types of leucosome: (1) Layer-parallel leucosomes that grew during deformation and prograde metamorphism. These are enriched in SiO₂, Sr, and Eu, but depleted in TiO₂, Fe₂O₃, MgO, Cs, Rb, REE, Sc, Th, Zr, and Hf relative to the Quetico metasediments. (2) Discordant leucosomes that formed after the regional folding events when metamorphic temperatures were at their peak. These are enriched in Rb, Ba, Sr and Eu, but display a wide range of LREE, Th, Zr, and Hf contents relative to the Quetico metasediments.
Layer-parallel leucosomes formed by a subsolidus process termed tectonic segregation. This stress-induced mass transfer process began when the Quetico sediments were deformed during burial, and continued whilst the rocks were both stressed and heterogeneous. Subsolidus leucosome compositions are consistent with the mobilization of quartz and feldspar from the host rocks by pressure solution. The discordant leucosomes formed by partial melting of the Quetico metasediments, possibly during uplift of the belt. The range of composition displayed by the anatectic leucosomes arises from crystal fractionation during leucosome emplacement. Some anatectic leucosomes preserve primary melt compositions and have smooth REE patterns, but those with negative Eu anomalies represent fractionated melts, and others with positive Eu anomalies represent accumulations of feldspar plus trapped melt.     

Petrogenesis of a Stromatic Migmatite (Nelaug, Southern Norway)

The stromatic migmatites of Nelaug (Tvedestrand area, SouthernNorway) are investigated in detail. They show well developedlayers of leucosomes, mesosomes and melanosomes. It is establishedthat the mesosomes and leucosomes of these migmatites are differentfrom each other texturally, mineralogically, and chemically.Also combinations of leucosome plus adjacent melanosome portionsare chemically different from those of the mesosomes. Theseobservations do not agree with the findings of Mehnert (1971)and do not fit into his genetic model. The mesosome layers and the leucosome + melanosome combinationsare taken to represent the chemical compositions of the countryrock, a metagraywacke with relicts of primary rhythmic layering(Touret, 1965). The mineralogical composition of the layersvaries from granitic to tonalitic. Relict textures indicatethat the leucosome portions were initially occupied by layersof granitic composition relatively rich in K-feldspar, whereasthe mesosomes are the representatives of those metagraywackelayers which were relatively rich in plagioclase. An almostisochemical transformation of a paragneiss into the investigatedstromatic migmatite is established. Melting experiments performed at PH₂O= 5 Kb yielded solidustemperatures of 640±7 °C for all layers. The Composition of plagioclases present in the different layersis explained by isochemical partial melting and in situ crystallization.The chemical, mineralogical, and textural findings support themodel of almost isochemical transformation already establishedfor the Arvika migmatites (Johannes & Gupta, 1982).     

Segregation of leucogranite microplutons during syn-anatectic deformation: an example from the Taylor Valley, Antarctica

A suite of migmatites in uppermost amphibolite facies schists of the Koettlitz Group exposed in the Taylor Valley, Antarctica, provides direct evidence of the behaviour of partially molten rock during syn-anatectic deformation. The geometry of the migmatites is directly related to their position relative to the hinge of a kilometre-scale antiform. Migmatitic rocks on the fold limbs are characterized by extensional shears and fractures, filled with leucosome material, that intersect the pervasive foliation and millimetre-thick stromatic leucosomes. Vein- and dyke-like leucosomes become more common and thicker from the limb to the hinge region of the antiform. Rocks characterized by high leucosome-to-rock ratios near the antiform hinge are xenolithic in appearance. Major parasitic folds within the hinge contain leucogranite 'microplutons' up to 50 m across beneath refractory 'cap-rock' layers.
Angular boudinage structures in schists surrounded by leucosomes indicate a relatively low yield strength in the leucosome, which is compatible with a molten rather than solid leucosome. Leucogranite-bearing extensional shears and fractures indicate that repeated extensional fracturing and shearing promoted by high fluid (melt) pressure is an important mechanism of melt segregation. Dilation in the hinges of developing folds aids the migration of melt into fold hinges and the development of 10–50-m-wide 'microplutons' of xenolith-rich leucogranite.
Lack of vapour-absent melting and consequent low melt-to-rock ratios allowed the Koettlitz Group to maintain its structural coherency on a kilometre scale. Consequently, leucosome 'microplutons' did not exceed 50 m in width, and therefore observed leucosomes have not contributed to the development of adjacent plutonic-scale granitoids.     

Origin of CO2-rich fluid inclusions in leucosomes from the Skagit migmatites, North Cascades, Washington, USA

CO₂–CH₄ fluid inclusions are present in anatectic layer-parallel leucosomes from graphite-bearing metasedimentary rocks in the Skagit migmatite complex, North Cascades, Washington. Petrological evidence and additional fluid inclusion observations indicate, however, that the Skagit Gneiss was infiltrated by a water-rich fluid during high-temperature metamorphism and migmatization. CO₂-rich fluid inclusions have not been observed in Skagit metasedimentary mesosomes or melanosomes, meta-igneous migmatites, or unmigmatized rocks, and are absent from subsolidus leucosomes in metasedimentary migmatites. The observation that CO₂-rich inclusions are present only in leucosomes interpreted to be anatectic based on independent mineralogical and chemical criteria suggests that their formation is related to migmatization by partial melting. Although some post-entrapment modification of fluid inclusion composition may have occurred during decompression and deformation, the generation of the CO₂-rich fluid is attributed to water-saturated partial melting of graphitic metasedimentary rocks by a reaction such as biotite + plagioclase + quartz + graphite ± Al₂SiO₅+ water-rich fluid = garnet + melt + CO₂–CH₄. The presence of CO₂-rich fluid inclusions in leucosomes may therefore be an indication that these leucosomes formed by anatexis. Based on the inferences that (1) an influx of fluid triggered partial melting, and (2) some episodes of fluid inclusion trapping are related to migmatization by anatexis, it is concluded that a free fluid was present at some time during high-temperature metamorphism. The infiltrating fluid was a water-rich fluid that may have been derived from nearby crystallizing plutons. Because partial melting took place at pressures of at least 5 kbar, abundant free fluid may have been present in the crust during orogenesis at depths of at least 15 km.     

The link between oxygen isotope resetting, partial melting, and fluid flow in metamorphic terrains

A correlation between the style of partial melting and synmeta-morphic fluid flow exists in metapelites from the Mount Lofty Ranges, Reynolds Range, and Omeo Zone (Australia). Mount Lofty Ranges migmatites comprise granitic leucosomes in rocks that are still biotite rich, with no indications of other mafic minerals being formed along with the melts. By contrast, in the Reynolds and Omeo migmatites, garnet, cordierite, and/or spinel formed along with the melts. Oxygen isotope data are most consistent with the Mount Lofty Ranges undergoing significant fluid–rock interaction during regional metamorphism, which may have fluxed fluid-present partial melting. By contrast regional metamorphic fluid flow in the Reynolds Range and Omeo Zone was limited, leading to partial melting via fluid-absent reactions. The style of melting reactions may help to constrain the timing of isotopic resetting and fluid flow in metamorphic terrains, which is currently a contentious issue.     

The processes that control leucosome compositions in metasedimentary granulites: perspectives from the Southern Marginal Zone migmatites,Limpopo Belt,South Africa

Anatexis of metapelitic rocks at the Bandelierkop Quarry (BQ) locality in the Southern Marginal Zone of the Limpopo Belt occurred via muscovite and biotite breakdown reactions which, in order of increasing temperature, can be modelled as: (1) Muscovite + quartz + plagioclase = sillimanite + melt; (2) Biotite + sillimanite + quartz + plagioclase = garnet + melt; (3) Biotite + quartz + plagioclase = orthopyroxene ± cordierite ± garnet + melt. Reactions 1 and 2 produced stromatic leucosomes, which underwent solid‐state deformation before the formation of undeformed nebulitic leucosomes by reaction 3. The zircon U–Pb ages for both leucosomes are within error identical. Thus, the melt or magma formed by the first two reactions segregated and formed mechanically solid stromatic veins whilst temperature was increasing. As might be predicted from the deformational history and sequence of melting reactions, the compositions of the stromatic leucosomes depart markedly from those of melts from metapelitic sources. Despite having similar Si contents to melts, the leucosomes are strongly K‐depleted, have Ca:Na ratios similar to the residua from which their magmas segregated and are characterized by a strong positive Eu anomaly, whilst the associated residua has no pronounced Eu anomaly. In addition, within the leucosomes and their wall rocks, peritectic garnet and orthopyroxene are very well preserved. This collective evidence suggests that melt loss from the stromatic leucosome structures whilst the rocks were still undergoing heating is the dominant process that shaped the chemistry of these leucosomes and produced solid leucosomes. Two alternative scenarios are evaluated as generalized petrogenetic models for producing Si‐rich, yet markedly K‐depleted and Ca‐enriched leucosomes from metapelitic sources. The first process involves the mechanical concentration of entrained peritectic plagioclase and garnet in the leucosomes. In this scenario, the volume of quartz in the leucosome must reflect the remaining melt fraction with resultant positive correlation between Si and K in the leucosomes. No such correlation exists in the BQ leucosomes and in similar leucosomes from elsewhere. Consequently, we suggest disequilibrium congruent melting of plagioclase in the source and consequential crystallization of peritectic plagioclase in the melt transfer and accumulation structures rather than at the sites of biotite melting. This induces co‐precipitation of quartz in the structures by increasing SiO₂ content of the melt. This process is characterized by an absence of plagioclase‐induced fractionation of Eu on melting, and the formation of Eu‐enriched, quartz + plagioclase + garnet leucosomes. From these findings, we argue that melt leaves the source rapidly and that the leucosomes form incrementally as melt or magma leaving the source dumps its disequilibrium Ca load, as well as quartz and entrained ferromagnesian peritectic minerals, in sites of magma accumulation and escape. This is consistent with evidence from S‐type granites suggesting rapid magma transfer from source to high level plutons. These findings also suggest that leucosomes of this type should be regarded as constituting part of the residuum from partial melting.     

Partial melting in the Inzie Head gneisses: the role of water and a petrogenetic grid in KFMASH applicable to anatectic pelitic migmatites

A sequence of prograde isograds is recognized within the Dalradian Inzie Head gneisses where pelitic compositions have undergone variable degrees of partial melting via incongruent melting reactions consuming biotite. Three leucosome types are identified. At the lowest grades, granitic leucosomes containing porphyroblasts of cordierite (CRD‐melt) are abundant. At intermediate grades, CRD‐melt mingles with garnetiferous leucosomes (GT‐melt). At the highest grades, CRD‐melt coexists with orthopyroxene‐bearing leucosomes (OPX‐melt), while garnet is conspicuously absent. The prograde metamorphic field gradient is constrained to pressures of 2–3 kbar below the CRD‐melt isograd, and no greater than 4.5 kbar at the highest grade around Inzie Head. A petrogenetic grid, calculated using thermocalc , is presented for the K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O (KFMASH) system for the phases orthopyroxene, garnet, cordierite, biotite, sillimanite, H₂O and melt with quartz and K‐feldspar in excess. For the implied field gradient, the reaction sequence predicted by the grid is consistent with the successive prograde development of each leucosome type. Compatibility diagrams suggest that, as anatexis proceeded, bulk compositions may have been displaced towards higher MgO content by the removal of (relatively) ferroan granitic leucosome. An isobaric (P = 4 kbar) T–a_H2O diagram shows that premigmatization fluids must have been water‐rich (a_H2O > 0.85) and suggests that, following the formation of small volumes of CRD‐melt, the system became fluid‐absent and melting reactions buffered a_H2O to lower values as temperatures rose. GT‐ and OPX‐melt formed by fluid‐absent melting reactions, but a maximum of 7–11% CRD‐melt fraction can be generated under fluid‐absent conditions, much less than the large volumes observed in the field. There is strong evidence that the CRD‐melt leucosomes could not have been derived by buoyantly aided upwards migration from levels beneath the migmatites. Their formation therefore required a significant influx of H₂O‐rich fluid, but in a quantity insufficient to have exhausted the buffering capacity of the solid assemblage plus melt. Fluid : rock ratios cannot have exceeded 1 : 30. The fluid was channelled through a regionally extensive shear zone network following melt‐induced failure. Such an influx of fluid at such depths has obvious consequences for localized crustal magma production and possibly for cordierite‐bearing granitoids in general.     

大陆造山带深熔垮塌的岩石学、地球化学证据:以北大别深熔混合岩为例

北大别位于大别造山带的核部,分布着大量的造山带垮塌时期形成的混合岩,其于理解大别造山带的形成和演化有着重要的意义。北大别混合岩的原岩为TTG（D）岩石,因黑云母和角闪石的脱水熔融诱发深熔作用产生。顺层产出的为富斜长石浅色体,主要矿物组成为斜长石+石英+黑云母±钾长石±角闪石。伟晶岩脉或团块为富钾长石浅色体,主要矿物组成为钾长石+石英±斜长石±黑云母±角闪石。暗色体为变晶结构,主要矿物组成为角闪石+黑云母+斜长石+石英±单斜辉石;其中,暗色矿物角闪石和黑云母常常定向排列,具有明显的溶蚀结构;暗色体中浅色矿物颗粒较小,以斜长石和石英为主,指示部分熔融的残余产物。全岩地球化学特征表明,碱金属元素（Na、K等）、大离子亲石元素（Ba、K、La等）和LREE等优先进入酸性熔体,而相容元素和中-重稀土元素等残留在残余体中。浅色体与本区花岗岩相比,二者都有右倾的稀土配分模式,富集LREE,亏损HREE。但浅色体具有明显的Eu正异常,δEu值为2.48~6.55,而花岗岩则有弱的Eu负异常,并且浅色体中大颗粒斜长石相互构成框架结构,含量明显高于正常花岗岩熔体,表明浅色体更可能是熔体早期结晶的产物。     

Tertiary deep crustal ultrametamorphism in the Hidaka metamorphic belt, northern Japan

The Main Zone of the Hidaka metamorphic belt is an imbricate stack of crustal material derived from an island arc in which a sequence of units with increasing metamorphic grade from low to high structural levels is exposed. The basal part of the metamorphic sequence underwent granulite facies metamorphism with peak P–T conditions of 7kbar, 870°C. In this zone pelitic granulite includes leucosomes which consist mainly of orthopyroxene-plagioclase-quartz.
To test whether the leucosome was derived by partial melting of the surrounding pelite, melting experiments of the pelitic granulite were carried out for water-saturated and dry systems at 7 kbar and 850°C. The chemical composition of the leucosome produced during these runs shows a peraluminous S-type tonalitic affinity and is located very close to the tie-line between the average melts produced in water-saturated systems and the average composition of the residual orthopyroxene + plagioclase. This therefore suggests that the lecosome in pelitic granulite was formed by incipient anatexis at close to the highest P–T condition of the Main Zone.
The age of the crustal anatexis is determined by the Rb-Sr whole rock isochron method for garnet-cordierite-biotite gneiss (host rock), garnet-orthopyroxene-cordierite gneiss (restite) and S-type tonalite (melt). This gives an age of 56.0 Ma with an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.705711. The S-type tonalite magmas that form large intrusive masses in the Main Zone were probably generated by crustal anatexis in deeper parts of the crust at the same time (late Palaeocene).