高级变质岩中深熔作用的相平衡研究

深熔作用在高级变质岩中非常普遍并受到广泛关注。自20世纪90年代以来,随着变质相平衡研究的突破性发展,利用THERMOCALC程序和视剖面图方法可以定量研究固相线以上的熔体形成、熔体分馏和退变质反应。变质沉积岩中的熔融作用主要有三种机制饱和水固相线上的熔融、白云母脱水熔融和黑云母脱水熔融。在模拟泥质岩石的KFMASH体系和NCKFMASH体系中的相平衡计算表明,NCKFMASH体系中铁镁矿物的相平衡关系受KFMASH亚体系中矿物相平衡关系的控制,但KFMASH亚体系中固相线位置要比实际的高50~60℃。因此,模拟泥质岩石的固相线以上的相平衡关系最好在NCKFMASH或组分更多的体系中进行。相平衡研究表明麻粒岩相岩石的保存与熔体丢失有关;混合岩的形成过程包括部分熔融作用、不同程度熔体分凝与汲取和不同程度的逆反应和退变反应。     

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.     

Fluid-present anatexis of metapelites at El Joyazo (SE Spain): constraints from Raman spectroscopy of graphite

The garnet-biotite-sillimanite anatectic xenoliths in the Neogene dacite dome of El Joyazo (also called Cerro de Hoyazo, SE Spain) contain four types of graphite (I to IV), distinguished on the basis of grain size and texture. Structural characterization of graphite by Laser Raman spectroscopy (LRS) shows systematic differences in the degree of ordering among the four types: only type III is fully consistent with the granulite-facies conditions reached by the xenoliths during partial melting, the others indicate metamorphic temperatures covering amphibolite-facies conditions, with only a few examples of granulite-grade crystallinity. All graphite crystallized before or during the anatectic event, indicating that a large fraction of the graphite did not equilibrate at peak temperatures. The mm-scale coexistence of different types and degrees of ordering in the graphite suggests different origins, i.e. of biogenic derivation and “fluid-deposited”, and is explained in terms of fluid-melt-graphite interaction during the anatectic event. Disequilibrium behaviour during high-temperature metamorphism and anatexis is typical of types I, II and particularly of IV, and is attributed to sluggish kinetics of solid-state graphitization, mainly owing to the limited time of the process and carbon saturation of the intergranular fluid. The coexisting, well-ordered type III graphite is the product of melting in the presence of a graphite-saturated fluid, a process that would account for the deposition of new graphite. The LRS results, together with petrologic observations, suggest that it is possible that high melt fractions can be generated by fluid-present melting of a metasedimentary protolith also in a closed system. Although this contradicts the commonly accepted hypothesis that, due to limited rock porosities, extensive fluid-present melting is precluded unless infiltration occurs, it is a possible end-member model in anatectic settings characterized by rapid heating rates and low-grade source rocks. Received: 14 July 1998 / Accepted: 16 November 1998     

High-grade metamorphism and hydrous melting of metapelites in the Pinos terrane (W Cuba): Evidence for crustal thickening and extension in the northern Caribbean collisional belt

The Pinos terrane (Isle of Pines, W Cuba) is a coherent metamorphic complex that probably represents a portion of the continental margin of the Yucatan Block during the Mesozoic. Within the framework of other metamorphic terranes in the Greater Antilles, the Pinos terrane is characterized by the occurrence of high‐grade kyanite‐, sillimanite‐ and andalusite‐bearing metapelites and migmatites. Assessment and modelling of phase relations in these high grade rocks indicate that they reached a peak temperature of c. 750 °C at 11–12 kbar, and then underwent strong decompression to c. 3 kbar at c. 600 °C. Decompression was contemporaneous with the main synmetamorphic deformation in the area (D2), and was accompanied by segregation of trondhjemitic partial melts formed by wet melting of metapelites. Metamorphism terminated in the Uppermost Cretaceous (68 ± 2 Ma; ⁴⁰Ar/³⁹Ar dates on biotite and muscovite). The P–T–t‐deformation relations of the high‐grade rocks suggest that crustal thickening (during collision of this portion of the Yucatan margin with the Great Volcanic Arc of the Caribbean?) was followed by decompression interpreted to reflect exhumation by extension, possibly related to the initial development of the Yucatan Basin in the uppermost Cretaceous.     

Palaeoproterozoic high-T, low-P metamorphism and dehydration melting in metapelites from the Mopunga Range, Arunta Inlier, central Australia

A sequence of psammitic and pelitic metasedimentary rocks from the Mopunga Range region of the Arunta Inlier, central Australia, preserves evidence for unusually low pressure (c. 3 kbar), regional‐scale, upper amphibolite and granulite facies metamorphism and partial melting. Upper amphibolite facies metapelites of the Cackleberry Metamorphics are characterised by cordierite‐andalusite‐K‐feldspar assemblages and cordierite‐bearing leucosomes with biotite‐andalusite selvages, reflecting P–T conditions of c. 3 kbar and c. 650–680 °C. Late development of a sillimanite fabric is interpreted to reflect either an anticlockwise P–T evolution, or a later independent higher‐P thermal event. Coexistence of andalusite with sillimanite in these rocks appears to reflect the sluggish kinematics of the Al₂SiO₅ polymorphic inversion. In the Deep Bore Metamorphics, 20 km to the east, dehydration melting reactions in granulite facies metapelites have produced migmatites with quartz‐absent sillimanite‐spinel‐cordierite melanosomes, whilst in semipelitic migmatites, discontinuous leucosomes enclose cordierite‐spinel intergrowths. Metapsammitic rocks are not migmatised, and contain garnet–orthopyroxene–cordierite–biotite–quartz assemblages. Reaction textures in the Deep Bore Metamorphics are consistent with a near‐isobaric heating‐cooling path, with peak metamorphism occurring at 2.6–4.0 kbar and c. 750–800 °C. SHRIMP U–Pb dating of metamorphic zircon rims in a cordierite‐orthopyroxene migmatite from the Deep Bore Metamorphics yielded an age of 1730 ± 7 Ma, whilst detrital zircon cores define a homogeneous population at 1805 ± 7 Ma. The 1730 Ma age is interpreted to reflect the timing of high‐T, low‐P metamorphism, synchronous with the regional Late Strangways Event, whereas the 1805 Ma age provides a maximum age of deposition for the sedimentary precursor. The Mopunga Range region forms part of a more extensive low‐pressure metamorphic terrane in which lateral temperature gradients are likely to have been induced by localised advection of heat by granitic and mafic intrusions. The near‐isobaric Palaeoproterozoic P–T–t evolution of the Mopunga Range region is consistent with a relatively transient thermal event, due to advective processes that occurred synchronous with the regional Late Strangways tectonothermal event.     

西藏南部南迦巴瓦地区中新世-上新世地壳深熔作用

位于喜马拉雅东构造结的南迦巴瓦地块经历了复杂的构造变形、强烈的变质和深熔作用,是研究碰撞造山过程中地壳深熔作用的重要对象。完整地厘定新生代晚期岩浆作用期次对于揭示南迦巴瓦地区的构造演化历史和深部过程具有重要意义。南迦巴瓦地块3件淡色花岗岩样品的锆石U-Pb定年结果显示该地块经历了11.30±0.16Ma和2.59±0.04Ma两期地壳深熔作用,可能与南迦巴瓦地块晚新生代快速隆升和剥蚀相关。南迦巴瓦地块保存了大量的~11Ma变质作用和地壳深熔作用记录指示该时间段为构造活动剧烈期。上新世晚期的淡色花岗岩表明,穹窿的隆升和剥蚀所导致的岩浆作用至少持续到了~2.59Ma,代表了南迦巴瓦地区一次年轻的构造岩浆事件。

     

喜马拉雅碰撞造山带新生代地壳深熔作用与淡色花岗岩

自从印度-欧亚大陆碰撞以来,伴随着构造演化和温度-压力-成分(P-T-X)的变化,喜马拉雅造山带中下地壳变质岩发生不同类型的部分熔融反应,形成性质各异的过铝质花岗岩。这些花岗岩在形成时代、矿物组成、全岩元素和放射性同位素地球化学特征上都表现出巨大的差异性。始新世构造岩浆作用形成高Sr/Y二云母花岗岩和演化程度较高的淡色花岗岩和淡色花岗玢岩,它们具有相似的Sr-Nd同位素组成,是碰撞早期增厚下地壳部分熔融的产物。渐新世淡色花岗岩主要为演化程度较高的淡色花岗岩,可能指示了喜马拉雅造山带的快速剥露作用起始于渐新世。早中新世以来的淡色花岗岩是喜马拉雅造山带淡色花岗岩的主体,是变泥质岩部分熔融的产物,包含两类部分熔融作用——水致白云母部分熔融作用(A类)和白云母脱水熔融作用(B类)。这两类部分熔融作用形成的花岗质熔体在元素和同位素地球化学特征上都表现出明显的差异性,主要受控于两类部分熔融作用过程中主要造岩矿物和副矿物的溶解行为。这些不同期次的地壳深熔作用都伴随着高分异淡色花岗岩,伴随着关键金属元素(Nb、Ta、Sn、Be等)的富集,是未来矿产勘探的重要靶区。新的观测结果表明:在碰撞造山带中,花岗岩岩石学和地球化学性质的变化是深部地壳物质对构造过程响应的结果,是深入理解碰撞造山带深部地壳物理和化学行为的重要岩石探针。     

Tracking fluid flow during deep crustal anatexis: metasomatism of peridotites (Naxos, Greece)

Horizons of ultramafic lenses were metamorphosed with host felsic gneisses at upper amphibolite facies conditions during the M2 event on the island of Naxos, Greece. The synkinematic peak M2 Ol-Opx-Hbl-Chl-Spl assemblage of the Main, migmatite-associated, Ultramafic Horizon (MUH) retains mantle-like chemical and oxygen isotope compositions and thus shows no evidence of infiltration of fluids from the host rocks. A bimodal distribution of temperatures, grouped at 700 and 1,200 °C, is given by oxygen isotope Opx-Ol thermometry in the MUH meta-peridotites and indicates partial oxygen exchange during M2 superposed over previous mantle fractionation. The Agia Ultramafic Horizon (AUH), a coarser-grained and unfoliated peridotite, occurs within sillimanite gneisses in northwest Naxos and contains talc-enstatite and olivine domains. Recrystallization of the AUH peridotite during post-peak M2 infiltration of silica-rich, high '¹⁸O fluids is indicated by lack of deformation, increased activity of silica required to stabilize the talc-enstatite assemblage, extremely high '¹⁸O values of Ol and Opx and (¹⁸O_(Opx-Ol) temperatures of 520-650 °C. The source for these fluids is inferred to be aplitic and pegmatitic dikes emanating from the migmatitic core of Naxos and intruding the AUH. At peak M2 temperatures and during anatexis of gneisses, volumes of fluid were small and fluid composition was locally buffered in the deeper part of the Naxos section. Crystallization of melts within the migmatitic core released siliceous fluids and initiated an episode of retrograde hydrous metamorphism in the overlying sequences, as observed in the AUH.     

HTLP metamorphism and fluid-fluxed melting during multistage anatexis of continental crust (N Sardinia,Italy)

The Variscan high-grade metamorphic basement of northern Sardinia and southern Corsica record lower Carboniferous anatexis related to post-collisional decompression of the orogen. Migmatites exposed in the Punta Bianca locality (Italy) consist of quartz + biotite + plagioclase + K-feldspar orthogneisses, garnet and cordierite-bearing diatexite and metatexites, derived from metasediments. Field evidence, petrographic observations, ELA-ICP-MS zircon and monazite dating and pseudosection modelling suggest that anatexis was apparently episodic involving two main stages of partial melting. Using pseudosection modelling, we infer that the first stage of partial melting is in the upper amphibolite facies (~0.45 GPa at ~740°C). Cordierite overgrowths replacing sillimanite, combined with the composition of plagioclase and K-feldspar, suggest decompression followed cooling below the solidus at low pressures of ~0.3 GPa. The age of the first anatectic event is not precisely constrained because of extensive resetting of the isotopic systems during the second melting stage, yet few zircons preserve a lower Carboniferous age which is consistent with the regional dataset. This lower Carboniferous migmatitic fabric is offset by a network of pseudotachylyte-bearing faults suggestive of cooling to greenschist facies conditions. Garnet/cordierite-bearing diatexites incorporate fragments of pseudotachylite-bearing orthogneiss and metatexites. Pseudosection modelling indicates nearly isobaric re-heating up to ~750°C, followed by further cooling below the solidus. The inferred P–T path is consistent with decompression and cooling of the Variscan crust through post-collisional extension and collapse of the thickened orogenic crust, followed by nearly isobaric re-heating at low pressures (~0.3 GPa) yielding to a second melting stage under LP-HT conditions. U/Th-Pb monazite ages for diatexite migmatites indicate an upper bound of 310–316 Ma for the second melting stage, suggesting that the second melting stage is coincident with the regional phase of crustal shearing. The cause of the high geothermal gradient required for re-heating during the second melting stage is unknown but likely requires some heat source that was probably related to dissipation of mechanical work within crustal-scale shear zones. According to this interpretation, some upper Carboniferous peraluminous granite precursors of the Corsica–Sardinia Batholith could be the outcome rather than the cause of the late-Variscan high-T metamorphism.     

Two-stage growth of porphyroblastic biotite and garnet in the Barrovian metapelites of the Imjingang belt, central Korea

Porphyroblastic biotite and garnet in the Barrovian metapelites of the Imjingang belt, Korea, were investigated to unravel the sequence and mechanism of mineral growth. Poikiloblastic biotite contains straight inclusion trails (S_i) discontinuous to the major foliation, and develops clear zones at the grain margin. These microstructures suggest an initial growth of biotite between two contractional deformations (D_n−1 and D_n) followed by an overgrowth during D_n. Although garnet poikiloblasts contain variable S_i patterns, their major growth is likely to have occurred during D_n on the basis of compositional relationships among variable garnet types. Early poikiloblasts of both minerals were formed by chemical replacement of the matrix that consisted mainly of chlorite, muscovite and quartz. Subsequent growth of biotite was governed by a crack-filling mechanism, and was accompanied by the production of extensional cracks inside or around biotite, providing fluid pathways. The overgrowth of garnet was favoured at the biotite–garnet interface, and the consequence was a partial replacement of inclusion-poor garnet after biotite subsequent to D_n. In addition, clear zones and pressure shadows as well as the matrix around biotite porphyroblasts were replaced by garnet, suggesting an inheritance of various pre-existing microstructures in the S_i pattern of garnet. Further attention is thus required for any attempt to delineate the microstructural interaction between deformation and metamorphism, particularly in a sample containing early-grown porphyroblasts. Microstructural evidence for the two-stage growth of biotite and garnet is present up to the kyanite zone, indicating that this growth mechanism is prevalent during progressive metamorphism of Barrovian metapelites.     

Cordierite as a sensor of fluid conditions in high-grade metamorphism and crustal anatexis

Cordierite H₂O and CO₂ volatile saturation surfaces derived from recent experimental studies are presented for P–T conditions relevant to high‐grade metamorphism and used to evaluate fluid conditions attending partial melting and granulite formation. The volatile saturation surfaces and saturation isopleths for both H₂O and CO₂ in cordierite are strongly pressure dependent. In contrast, the uptake of H₂O by cordierite in equilibrium with melts formed through biotite dehydration melting, controlled by the distribution of H₂O between granitic melt and cordierite, D_w[D_w = wt% H₂O (melt)/wt% H₂O(Crd)], is mainly temperature dependent. D_w = 2.5–6.0 for the H₂O contents (0.4–1.6 wt percentage) typical of cordierite formed through biotite dehydration melting at 3–7 kbar and 725–900 °C. This range in D_w causes a 15–30% relative decrease in the total wt% of melt produced from pelites. Cordierite in S‐type granites are H₂O‐rich (1.3–1.9 wt%) and close to or saturated in total volatiles, signifying equilibration with crystallizing melts that achieved saturation in H₂O. In contrast, the lower H₂O contents (0.6–1.2 wt percentage) preserved in cordierite from many granulite and contact migmatite terranes are consistent with fluid‐absent conditions during anatexis. In several cases, including the Cooma migmatites and Broken Hill granulites, the cordierite volatile compositions yield a_H2O values (0.15–0.4) and melt H₂O contents (2.2–4.4 wt%) compatible with model dehydration melting reactions. In contrast, H₂O leakage is indicated for cordierite from Prydz Bay, Antarctica that preserve H₂O contents (0.5–0.3 wt%) which are significantly less than those required (1.0–0.8 wt%) for equilibrium with melt at conditions of 6 kbar and 860 °C. The CO₂ contents of cordierite in migmatites range from negligible (< 0.1 wt%) to high (0.5–1.0 wt%), and bear no simple relationship to preserved cordierite H₂O contents and a_H2O. In most cases the cordierite volatile contents yield total calculated fluid activities (a_H2O + a_CO2) that are significantly less than those required for fluid saturation at the P–T conditions of their formation. Whether this reflects fluid absence, dilution of H₂O and CO₂ by other components, or leakage of H₂O from cordierite is an issue that must be evaluated on a case‐by‐case basis.     

Geological context of crustal anatexis and granitic magmatism in the northeastern Glenelg River Complex,western Victoria

The Cambro‐Ordovician Glenelg River Complex in the Harrow district, western Victoria, consists of extensive granitic rocks associated with a migmatitic metasedimentary envelope. Metasedimentary rocks comprise amphibolite facies massive‐laminated quartzo‐feldspathic schists and layered gneisses with minor sillimanite‐bearing horizons. Intercalated are stromatic and nebulitic migmatites of granitic and tonalitic character; textural evidence suggests that both varieties developed by in situ partial melting. Ranging from adamellite to leucotonalite, granitic rocks contain abundant magmatic muscovite, commonly with garnet and sillimanite, and exhibit generally unrecrystallised igneous textures. Heterogeneous structurally concordant plutons transitional to migmatites and more uniform intrusive phases are delineated with both types hosting diverse metasedimentary enclaves, micaceous selvages and schlieren; a gneissic foliation of variable intensity is defined by the latter. These petrographic attributes are consistent with derivation of plutons by anatexis of a peraluminous metasedimentary protolith. The schlieric foliation is not tectonically imposed, but rather directly inherited from the migmatitic precursor, compositional variations within which are preserved by the layered Schofield Adamellite. The most mafic granitic body (Tuloona Granodiorite) also has igneous microgranular enclaves indicating a more complex petrogenesis. Metasedimentary rocks experienced five episodes of folding, the latest involving macroscopic open warps. This is analogous to the structural history elucidated elsewhere in the Glenelg River Complex, by inference a coherent tectonic entity whose present metamorphic and stratigraphic configuration might be governed by F₅ folding. Structures within migmatites intimate that partial melting proceeded throughout the deformational history and peaked syn‐D₄ to pre‐D₅, whilst temperatures had waned to sub‐biotite grade in the southwestern Glenelg River Complex. Granitic rocks were generated during this anatectic culmination and were therefore emplaced late in the orogenic history relative to other syntectonic phases of the Glenelg River Complex.     

Dehydration melting and the granulite transition in metapelites from southern Namaqualand,S. Africa

In a prograde amphibolite-granulite transition zone in the Namaqualand Metamorphic Complex, metapelites show an interbanding of the amphibolite facies association biotite+sillimanite+quartz with the granulite facies association garnet+cordierite+K-feldspar. Relict graded bedding shows that compositional banding is of sedimentary origin. The garnet-cordierite-K-feldspar gneisses contain quartzofeldspathic segregations surrounding garnets, and have more Fe-rich bulk compositions than the biotite-sillimanite schists.The contrasting asemblages could have formed at the same pressure and temperature provided that a(H₂O) was systematically lower in the garnet-cordierite-K-feldspar layers. The a(H₂O) reduction resulted from the production of silicate melt by a vapour-absent continuous Fe-Mg reaction such as biotite+sillimanite+quartz=garnet+K-feldspar+liquid which affects Fe-rich compositions before vapour-absent melting occurs in more Mg-rich rocks. The segregations represent the solid and liquid products of the reaction.Such processes imply local control of a(H₂O), and indicate that this granulite transition did not result from a regional influx of metasomatising fluids.     

Incongruent melting of biotite to spinel in a quartz-free restite at El Joyazo (SE Spain): Textures and reaction characterization

In the Grt-Bt-Sil restitic xenoliths of El Joyazo (Cerro de Hoyazo), hercynitic spinel is a minor phase commonly associated with biotite. The possible reaction relationships among biotite and spinel are studied in reaction textures developed around biotites at their contact with patches of fibrolitic sillimanite and rhyolitic melt. In these textures, resorbed biotite crystals about 1 mm long are rimmed by a layer of glass <200 μm thick containing spinel and ilmenite; the same glass also fills embayments in biotite. Spinel forms euhedral crystals <100 μm in size, and ilmenite occurs as smaller anhedral crystals or needles, often intergrown with spinel. The homogeneous felt-like melt-sillimanite aggregate (“mix”) is richest in glass close to the reaction rim around biotite. Plagioclase and garnet are located >5 mm away from the reaction texture. Biotite is chemically zoned. Cores (Bt ₁ ) have X_Mg=0.35 ± 0.02 and Ti=0.58 ± 0.01 atoms; whereas the outer rims (Bt ₂ ) have X_Mg=0.45 ± 0.01 and Ti up to 0.68 atoms. The hercynite-rich spinel (Spl) has low ZnO content (<0.80 wt%) and X_Mg=0.26 ± 0.04. The chemical compositions of the mix aggregate represent linear combinations between sillimanite and a silica-rich melt. This melt (melt ₁ ) is different from that of the layer around biotite (melt ₂ ), which is also richer in Ca and alkalis. Garnet rims (Grt) have low Ca and Mn, and X_Mg=0.14. Plagioclase is characterized by large homogeneous cores (Pl ₁ , An_31 ± 2) and more calcic rims (Pl ₂ , An_49 ± 6). Matrix analysis in the 9-component (Al-Ca-Fe-K-Mg-Mn-Na-Si-Ti), 9-phase (Bt₁-Bt₂-Grt-Spl-Ilm-melt₂-mix-Pl₁-Pl₂) system provides the mass balance (in mole units):

Dehydration melting of micas in the Chilka Lake Khondalites: The link between the metapelites and granitoids

Garnet-sillimanite gneisses, locally known as khondalites, occur abundantly in the Chilka Lake granulite terrane belonging to the Eastern Ghats Proterozoic belt of India. Though their chemistry has been modified by partial melting, it is evident that the majority of these rocks are metapelitic, with some tending to be metapsammitic. Five petrographically distinct groups are present within the khondalites of which the most abundant group is characteristically low in Mg:Fe ratios — the main chemical discriminant separating the five groups. The variations in Mg:Fe ratios of the garnets, biotites, cordierites, orthopyroxenes and spinels from the metapelites are compatible with those in the bulk rocks. A suite of granitoids containing garnet, K-feldspar, plagioclase and quartz, commonly referred to as leptynites in Indian granulite terranes, are interlayered with khondalites on the scale of exposures; in a few spots, the intercalated layers are thin. The peraluminous character of the leptynites and presence of sillimanite trails within garnets in some of them suggest derivation of leptynites by partial melting of khondalites. Here we examine this connection in the light of results derived from dehydration melting experiments of micas in pelitic and psammitic rocks. The plots of leptynites of different chemical compositions in a (MgO + FeO)-Na₂O-K₂O projection match the composition of liquids derived by biotite and muscovite dehydration melting, when corrected for co-products of melting reactions constrained by mass balance and modal considerations. The melt components of the leptynites describe four clusters in the M-N-K diagram. One of them matches melts produced dominantly by muscovite dehydration melting, while three clusters correspond to melting of biotite. The relative disposition of the clusters suggests two trends, which can be correlated with different paths that pelitic and psammitic protoliths are expected to generate during dehydration melting. Thus the leptynites evidently represent granitoids which were produced by dehydration melting in metapelites of different compositions. The contents of Ti, Y, Nb, Zr and Th in several leptynites indicate departures from equilibrium melt compositions, and entrainment of restites is considered to be the main causative factor. Disequilibrium in terms of major elements is illustrated by leucosomes within migmatites developed in a group of metapelites. But the discrete leptynites that have been compared with experimental melts approach equilibrium melt compositions closely.     

Geochemical constraints on crustal anatexis: a case study from the Pan-African Damara granitoids of Namibia

 Major and trace element models of recently published vapour-absent mica dehydration melting experiments are used to identify granitoids generated by muscovite and biotite dehydration melting, and to distinguish between plagioclase-limited and biotite-limited, biotite dehydration melting. In the case of granitoids from the Pan-African Damara mobile belt (Namibia), many of the leucogranites and Salem-type granitoids may be modelled by biotite dehydration melting. The low Rb/Sr granitoids (e.g. Donkerhuk Onanis, Salem Onanis, Donkerhuk Nomatsaus, Salem Goas) probably reflect feldspar-limited, biotite dehydration melting (a pelitic source) whereas the high Rb/Sr suites (e.g. Bloedkoppie leucogranite, Stinkbank leucogranite, Salem Swakopmund, Leucocratic Stink bank granite) reflect biotite-limited, biotite dehydration melting (a greywacke source). Alaskites from the Damara belt have major element compositions which are consistent with muscovite dehydration melting, and their positive Eu anomalies are linked to high K₂O reflecting K-feldspar entrainment. Combined Zr and LREE (light rare earth element) solubility models indicate that insufficient time (probably less than 10⁴ years) had elapsed between melt generation and melt extraction to ensure that the alaskite melts attained their equilibrium concentrations of Zr and the LREEs. In contrast, the leucogranites and Salem-type granites have attained their equilibrium inventories of these trace elements. Combined Fe₂O₃ and MgO contents in some samples from two granitoids (the Salem Goas and Donkerhuk Onanis intrusions) are higher than those readily attainable by biotite dehydration melting indicating either: (1) that they contain a contribution from melts generated by incipient garnet breakdown or; (2) that they contain small amounts of an entrained ferromagnesian phase. Received: 24 April 1995/Accepted: 11 December 1995     

Incomplete reaction of plagioclase in experimental dehydration melting of amphibolite

Dehydration melting of a hornblende‐plagioclase mixture of amphibolitic composition was investigated at 1000°C and at 800 MPa and 1200 MPa. At 1200 MPa the reaction products are garnet, clinopyroxene, melt and relatively Ab‐rich plagioclase (An₄₇). At 800 MPa the products are orthopyroxene, clinopyroxene, magnetite, amphibole (pargasite) and An‐rich plagioclase (An₇₅). The melts are rich in plagioclase components (especially in Ab) and, when compared to tonalites, relatively poor in silica. The grainsize of the starting materials was ≤?5 μm in the 800 MPa and ≤?10 μm in the 1200 MPa runs. All run products show unchanged plagioclase cores, which are the remnants of a very sluggish reaction assumed to be controlled by dissolution/precipitation processes at the plagioclase grain boundaries. The results indicate that only local equilibrium could have been obtained in recent investigations on dehydration melting experiments in plagioclase‐bearing systems. The results also suggest that plagioclase compositions once formed may persist for a very long time, even in hot magma chambers, if the prevailing water activity is low.     

Partial melting and phase relations in high-grade metapelites: an experimental petrogenetic grid in the KFMASH system

Petrogenetic grids are a powerful tool for understanding metamorphic terrains and many theoretical grids have been suggested for the process of granulite formation in metapelitic rocks, via fluid-absent biotite melting reactions. However, application of these grids has been difficult due to the lack of suitable experimental constraints. We present here an experimentally determined and tightly constrained petrogenetic grid for KFMASH system metapelites which extends from 840–1000°C and 5.0–12.5 kbar. Sixty four experiments on three KFMASH, mineral-mix, bulk compositions (X _Mg=0.62, 0.74, 0.86) provide phase composition and assemblage data from which a grid can be derived and constrained. Reversal experiments and consideration of the phase composition data show the experiments to be close to equilibrium. The KFMASH univariant fluid-absent biotite melting reactions occur between 850 and 870°C at 5 kbar and between 900 and 915°C at 10 kbar. These reactions are connected to equilibria beyond the stability of biotite to develop a fixed framework within which the phase assemblage evolution of metapelitic rocks can be interpreted. The effect of minor components on phase equilibria is evaluated using the experimentally determined grid as a simple-system reference. The temperature at which melting occurs in metapelites is strongly controlled by the concentrations of titanium and fluorine in biotite. Pressure-temperature pseudosections presented for each of the experimental compositions show both the univariant and divariant reactions available to a particular bulk composition, clearly illustrating the possible evolution of the phase assemblage. The pseudosections also constrain the stability limits of     

Geochemistry of ultrahigh-pressure anatexis: fractionation of elements in the Kokchetav gneisses during melting at diamond-facies conditions

The Kokchetav complex in Kazakhstan contains garnet-bearing gneisses that formed by partial melting of metasedimentary rocks at ultrahigh-pressure (UHP) conditions. Partial melting and melt extraction from these rocks is documented by a decrease in K₂O and an increase in FeO + MgO in the restites. The most characteristic trace element feature of the Kokchetav UHP restites is a strong depletion in light rare earth elements (LREE), Th and U. This is attributed to complete dissolution of monazite/allanite in the melt and variable degree of melt extraction. In contrast, Zr concentrations remain approximately constant in all gneisses. Using experimentally determined solubilities of LREE and Zr in high-pressure melts, these data constrain the temperature of melting to ~1,000 °C. Large ion lithophile elements (LILE) are only moderately depleted in the samples that have the lowest U, Th and LREE contents, indicating that phengite retains some LILE in the residue. Some restites display an increase in Nb/Ta with respect to the protolith. This further suggests the presence of phengite, which, in contrast to rutile, preferentially incorporates Nb over Ta. The trace element fractionation observed during UHP anatexis in the Kokchetav gneisses is significantly different from depletions reported in low-pressure restites, where generally no LREE and Th depletion occurs. Melting at UHP conditions resulted in an increase in the Sm/Nd ratio and a decoupling of the Sm–Nd and Lu–Hf systems in the restite. Further subduction of such restites and mixing with mantle rocks might thus lead to a distinct isotopic reservoir different from the bulk continental crust.