Melting experiments on the enstatite-diopside join at 70–224 kbar,including the melting of diopside

 Melting relations on the enstatite−diopside (En, Mg₂Si₂O₆−Di, CaMgSi₂O₆) join, including the compositions of crystalline phases and melts coexisting along the solidi, were experimentally determined in the pressure range 70–224 kbar with a split-sphere anvil apparatus (USSA-2000). Melting is peritectic in enstatite-rich compositions at 70–124 kbar (1840–2100° C) and eutectic at higher pressures, while the diopside-rich clinopyroxene melts azeotropically at 70–165 kbar and up to 300° C lower temperatures than the eutectic. Orthopyroxene is replaced with enstatite-rich clinopyroxene at 120 kbar and 2090°C. First garnet with 17 mol% Di forms on the solidus at 158 kbar and 2100° C. Two garnets coexist on the solidus at 165–183 kbar and 2100° C, garnet coexists with CaSiO₃ perovskite at 183–224 kbar (2100–2230° C) and two coexisting perovskites are stable at higher pressures. The melting curve of diopside was determined at 80–170 kbar; the slope becomes negative at 140 kbar and 2155° C. At 170 kbar and 2100° C, diopside with 96% Di breaks down to garnet with 89% Di and CaSiO₃ perovskite. The new data were used to calculate an improved temperature-pressure phase diagram for the CMAS system, which can be useful for estimating the mineralogy of the Earth's upper mantle. Received: 15 October 1994 / Accepted: 15 October 1995     

Garnet + liquid equilibrium

New experiments were performed to determine saturation conditions for garnet and silicate liquid. Starting compositions were natural basalt powders ranging from komatiite to nephelinite, which were partially melted at pressures between 25 and 100 kbar. Rounded grains of natural pyrope or grossular were added to some experiments to induce garnet saturation, and to aid the segregation of liquid pools for microprobe analysis. Simple expressions describing K _eq as a function of P, T and liquid composition were calibrated by linear least squares analysis of the data from this, and other, studies. Since garnets do not often occur as phenocrysts, equations were designed to predict garnet compositions when P, T and a silicate liquid composition are given. The regression data have a pressure range of 20–270 kbar, and compositions as diverse as nephelinite and komatiite. These models should thus apply to a broad range of geological problems. The majorite component in garnet was found to increase with increasing P, but compositional effects are also important. A garnet saturation surface applied to liquids with chondritic compositions shows that such liquids crystallize garnet with Mj contents of 0.27–0.42 at 200 kbar. Models of Earth differentiation thus need to account not only for fractionation of majorite, but also for Fe-, Ca-, Na- and Ti-bearing garnet components, which occur in non-trivial quantities at high pressure. Since many models of igneous petrogenesis rely on mineral-melt partition coefficients for the minor elements Na, Ti, and Cr, partition coefficients for these elements were also examined. The K _d ^gar/liq for Na was found to be P-sensitive; Na contents of basalts may thus potentially yield information regarding depths of partial melting. Received : 28 May 1997 / 25 November 1997     

Exsolution lamellae in a clinopyroxene megacryst aggregate from Cenozoic basalt,Leizhou Peninsula,South China: petrography and chemical evolution

Petrographic investigations and electron microprobe analyses have been performed on a rare aggregate of clinopyroxene megacrysts collected from Cenozoic basalts in Yinfengling, Leizhou Peninsula of South China. The aggregate, composed of several clinopyroxene megacrysts, shows abundant exsolution lamellae of garnet (Grt) and orthopyroxene (Opx), and granular texture. Cr- and Ti-poor spinels are also present in this sample. They occur predominantly as Sp–Opx–Grt clusters (Cr# = 0.025–0.034) at the interspace between different megacrysts, and subordinately as bleb-shaped (Cr# = 0.025–0.034) or thin-lamella crystals (Cr# = 0.006–0.021) in clinopyroxene. Three different assemblages of exsolution are identified, namely (1) Sp (high Cr/Al) and Opx; (2) Grt–Opx; (3) Sp (low Cr/Al) and Opx. In addition, some garnets were likely developed as response to breakdown of the high-Cr/Al Sp. The homogeneous compositions in all constituent minerals and the good agreement between calculated Cpx/Grt partition coefficients (K _d’s) for trace elements and reference data strongly suggest a chemical equilibrium among coexisting minerals, probably attained by diffusion after the exsolution. Thermobarometric calculation based on exsolved assemblage yields a temperature of 900 ± 30°C and a pressure of 12 ± 2.2 kbar, corresponding to the present-day thermal gradient in the region. Much higher P–T estimates (T = 1,210 ± 30°C, P = 16.2 ± 3.5 kbar) are obtained for the reconstructed composition of cpx prior to exsolution. The contrast in thermal state before and after the exsolution might reflect the thermal evolution of the lithosphere beneath South China during the Cenozoic. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Petrogenesis of the amphibole-rich veins from the Lherz orogenic lherzolite massif (Eastern Pyrenees, France): a case study for the origin of orthopyroxene-bearing amphibole pyroxenites in the lithospheric mantle

The Lherz orogenic lherzolite massif (Eastern French Pyrenees) displays one of the best exposures of subcontinental lithospheric mantle containing veins of amphibole pyroxenites and hornblendites. A reappraisal of the petrogenesis of these rocks has been attempted from a comprehensive study of their mutual structural relationships, their petrography and their mineral compositions. Amphibole pyroxenites comprise clinopyroxene, orthopyroxene and spinel as early cumulus phases, with garnet and late-magmatic K₂O-poor pargasite replacing clinopyroxene, and subsolidus exsolution products (olivine, spinel II, garnet II, plagioclase). The original magmatic mineralogy and rock compositions were partly obscured by late-intrusive hornblendites and over a few centimetres by vein–wallrock exchange reactions which continued down to subsolidus temperatures for Mg–Fe. Thermobarometric data and liquidus parageneses indicate that amphibole pyroxenites started to crystallize at P ≥ 13 kbar and recrystallized at P < 12 kbar. The high Al^VI/Al^IV ratio (>1) of clinopyroxenes, the early precipitation of orthopyroxene and the late-magmatic amphibole are arguments for parental melts richer in silica but poorer in water than alkali basalts. Their modelled major element compositions are similar to transitional alkali basalt with about 1–3 wt% H₂O. In contrast to amphibole pyroxenites, hornblendites only show kaersutite as liquidus phase, and phlogopite as intercumulus phase. They are interpreted as crystalline segregates from primary basanitic magmas (mg=0.6; 4–6 wt% H₂O). These latter cannot be related to the parental liquids of amphibole pyroxenites by a fractional crystallization process. Rather, basanitic liquids mostly reused pre-existing pyroxenite vein conduits at a higher structural level (P ≤ 10 kbar). A continuous process of redox melting and/or alkali melt/peridotite interaction in a veined lithospheric mantle is proposed to account for the origin of the Lherz hydrous veins. The transitional basalt composition is interpreted in terms of extensive dissolution of olivine and orthopyroxene from wallrock peridotite by alkaline melts produced at the mechanical boundary layer/thermal boundary layer transition (about 45–50 km deep). Continuous fluid ingress allowed remelting of the deeper veined mantle to produce the basanitic, strongly volatiles enriched, melts that precipitated hornblendites. A similar model could be valid for the few orthopyroxene-rich hydrous pyroxenites described in basalt-hosted mantle xenoliths. Received: 15 September 1999 / Accepted: 31 January 2000     

Prograde and retrograde history of the Junction School eclogite,California, and an evaluation of garnet–phengite–clinopyroxene thermobarometry

Quantitative thermobarometry of inclusions in zoned garnet from a Franciscan eclogite block record a counter-clockwise P–T path from blueschist to eclogite and back. Garnet retains prograde zoning from inclusion-rich Alm₅₂Grs₃₀Pyp₆Sps₁₂ cores to inclusion-poor Alm₆₂Grs₂₅Pyp₁₂Sps₁ mantles, with overgrowths of highly variable composition. Barometry using the Waters–Martin version of the garnet–phengite–omphacite thermobarometer yields conditions of 7–15 kbar, 400–500°C (garnet cores), 18–22 kbar, ∼550°C (mantles), and 10–14 kbar, 350–450°C (overgrowths), in agreement with clinozoisite–sphene–rutile–garnet–quartz barometry. These pressures are ∼10–15 kbar less than those obtained using more recent, fully thermodynamic calibrations of the phengite–omphacite–garnet thermobarometer. Low early temperatures suggest that the block was subducted in a thermally mature subduction zone and not at the inception of subduction when prograde temperature is expected to be higher. Franciscan high-grade blocks likely represent crust subducted throughout the history of this convergent margin, rather than only at the inception of the subduction zone.     

Metamorphic <Emphasis Type="Italic">P</Emphasis>–<Emphasis Type="Italic">T</Emphasis> paths of the Zanhuang amphibolites and metapelites: constraints on the tectonic evolution of the Paleoproterozoic Trans-North China Orogen

Garnet-bearing metapelites and amphibolites are exposed in the south and middle parts of the Zanhuang complex, which is located in the central segment of the nearly NS-striking Trans-North China Orogen. These rocks preserve three metamorphic mineral assemblages forming at the prograde, peak and post-peak decompression stages. The prograde metamorphic stage (M₁) is represented by mineral inclusions within garnet porphyroblasts, the peak metamorphic stage (M₂) is represented by garnet rims and matrix minerals, whereas the retrograde stage (M₃) is represented by amphibole + plagioclase symplectite rimming garnet porphyroblasts in the amphibolites and biotite + plagioclase symplectite rimming garnet porphyroblasts in the metapelites. All garnet porphyroblasts in the metapelites preserve prograde chemical zoning except for the ubiquitous, quite narrow zones from the underwent post-peak decompression. It has been determined through thermobarometric computation that the metamorphic conditions are 650–710°C at 8.2−9.2 kbar for the M₁ (inclusion) assemblages, >810°C at >12.5 kbar for the metamorphic peak M₂ (matrix) assemblages, and 660–680°C at 4.4–4.5 kbar for the retrograde M₃ (symplectite) assemblages. These rocks are thus determined to have undergone metamorphism with clockwise P–T paths involving nearly isothermal decompression (ITD) segments, which is inferred to be related to the amalgamation of the Eastern and Western Blocks to form the coherent basement of the North China Craton along the Trans-North China Orogen in the late Paleoproterozoic (1.88–1.85 Ga).     

Dehydration melting of tonalites. Part II. Composition of melts and solids

 Dehydration melting of tonalitic compositions (phlogopite or biotite-plagioclase-quartz assemblages) is investigated within a temperature range of 700–1000°C and pressure range of 2–15 kbar. The solid reaction products in the case of the phlogopite-plagioclase(An₄₅)-quartz starting material are enstatite, clinopyroxene and potassium feldspar, with amphiboles occurring occasionally. At 12 kbar, zoisite is observed below 800°C, and garnet at 900°C. The reaction products of dehydration melting of the biotite (Ann₅₀)-plagioclase (An₄₅)-quartz assemblage are melt, orthopyroxene, clinopyroxene, amphibole and potassium feldspar. At pressures > 8 kbar and temperatures below 800°C, epidote is also formed. Almandine-rich garnet appears above 10 kbar at temperatures ≥ 750°C. The composition of melts is granitic to granodioritic, hence showing the importance of dehydration melting of tonalites for the formation of granitic melts and granulitic restites at pressure-temperature conditions within the continental crust. The melt compositions plot close to the cotectic line dividing the liquidus surfaces between quartz and potassium feldspar in the haplogranite system at 5 kbar and a _{H 2O} = 1. The composition of the melts changes with the composition of the starting material, temperature and pressure. With increasing temperature, the melt becomes enriched in Al₂O₃ and FeO+MgO. Potash in the melt is highest just when biotite disappears. The amount of CaO decreases up to 900°C at 5 kbar whereas at higher temperatures it increases as amphibole, clinopyroxene and more An-component dissolve in the melt. The Na₂O content of the melt increases slightly with increase in temperature. The composition of the melt at temperatures > 900°C approaches that of the starting assemblage. The melt fraction varies with composition and proportion of hydrous phases in the starting composition as well as temperature and pressure. With increasing modal biotite from 20 to 30 wt%, the melt proportion increases from 19.8 to 22.3 vol.% (850°C and 5 kbar). With increasing temperature from 800 to 950°C (at 5 kbar), the increase in melt fraction is from 11 to 25.8 vol.%. The effect of pressure on the melt fraction is observed to be relatively small and the melt proportion in the same assemblage decreases at 850°C from 19.8 vol.% at 5 kbar to 15.3 vol.% at 15 kbar. Selected experiments were reversed at 2 and 5 kbar to demonstrate that near equilibrium compositions were obtained in runs of longer duration. Received: 27 December 1995 / Accepted: 7 May 1996     

Sector-zoned augite megacrysts in Aleutian high alumina basalts: implications for the conditions of basalt crystallization and the generation of calc-alkaline series magmas

Several high alumina basalts from the Aleutian volcanic centers of Cold Bay and Kanaga Island contain large (up to 1.5 cm diameter) megacrysts of sector-zoned augite. The megacrysts are invariably euhedral with well developed {001}, {010} and {111} forms. All crystals display concentric bands that are rich in mineral and glass inclusions. The sector zonation typically occurs as well developed (010), (100), (111) and (110) sectors which grew at different rates. A comparison of the width of synchronous growth bands indicates that following relative growth rates: (111) ≫ (100) ∼ (110) > (010). Compositionally, SiO₂ and MgO abundances decrease, and TiO₂, Al₂O₃, FeO and Na₂O abundances increase in the different sectors in the order (111), (100) ∼ (110), (010). This order is identical to that deduced for the relative growth rates, implying that growth rate clearly had a role in the development of the sector zonation. Calculated pre-eruption H₂O contents of the basalts range from 1 to 3 wt% but actual (measured) post-eruption H₂O contents range from 0.01 to 0.3 wt%. Deteurium isotopic values are heavily depleted and range from −110 to −141‰ . Together these indicate significant vapor (H₂O) exsolution prior to eruption. Maximum H₂O abundances in primitive glass inclusions, thought to be most representative of the host liquid reservoir at the time of melt entrapment, systematically decrease from the core to the rim of one augite megacryst studied in detail. We conclude that the presence of sector-zoned augite is due to augite supersaturation and rapid crystallization brought about by magma decompression and volatile (H₂O) exsolution. The calculated pre-eruption H₂O contents of 1–3 wt% limit vapor exsolution and basalt crystallization to depths of less than 3 and more likely 1.5 km. Very rapid crystallization at very shallow depths makes it unlikely that the time scales between initial crystallization and final eruption are sufficient to permit appreciable amounts of fractional crystallization. Given that high alumina basalt fractionation is the dominant process for generating more evolved andesite, dacite and rhyolite magmas of the calc-alkaline suite, the inability of parental high alumina basalt to yield such derivative magmas in the low pressure environment places the likely site of fractionation in the high pressure environment, at or near the base of the crust. Received: 1 December 1997 / Accepted: 23 December 1998     

Garnet-bearing tonalitic porphyry from East Kunlun,Northeast Tibetan Plateau: implications for adakite and magmas from the MASH Zone

A garnet-bearing tonalitic porphyry from the Achiq Kol area, northeast Tibetan Plateau has been dated by SHRIMP U-Pb zircon techniques and gives a Late Triassic age of 213 ± 3 Ma. The porphyry contains phenocrysts of Ca-rich, Mn-poor garnet (CaO > 5 wt%; MnO < 3 wt%), Al-rich hornblende (Al₂O₃ ~ 15.9 wt%), plagioclase and quartz, and pressure estimates for hornblende enclosing the garnet phenocrysts yield values of 8–10 kbar, indicating a minimum pressure for the garnet. The rock has SiO₂ of 60–63 wt%, low MgO (<2.0 wt%), K₂O (<1.3 wt%), but high Al₂O₃ (>17 wt%) contents, and is metaluminous to slightly peraluminous (ACNK = 0.89–1.05). The rock samples are enriched in LILE and LREE but depleted in Nb and Ti, showing typical features of subduction-related magmas. The relatively high Sr/Y (~38) ratios and low HREE (Yb < 0.8 ppm) contents suggest that garnet is a residual phase, while suppressed crystallization of plagioclase and lack of negative Eu anomalies indicate a high water fugacity in the magma. Nd–Sr isotope compositions of the rock (εNd_T = −1.38 to −2.33; ⁸⁷Sr/⁸⁶Sr_i = 0.7065–0.7067) suggest that both mantle- and crust-derived materials were involved in the petrogenesis, which is consistent with the reverse compositional zoning of plagioclase, interpreted to indicate magma mixing. Both garnet phenocrysts and their ilmenite inclusions contain low MgO contents which, in combination with the oxygen isotope composition of garnet separates (+6.23‰), suggests that these minerals formed in a lower crust-derived felsic melt probably in the MASH zone. Although the rock samples are similar to adakitic rocks in many aspects, their moderate Sr contents (<260 ppm) and La/Yb ratios (mostly 16–21) are significantly lower than those of adakitic rocks. Because of high partition coefficients for Sr and LREE, fractionation of apatite at an early stage in the evolution of the magma may have effectively decreased both Sr and LREE in the residual melt. It is suggested that extensive crystallization of apatite as an early phase may prevent some arc magmas from evolving into adakitic rocks even under high water fugacity.     

An experimental study of Ca-(Fe,Mg) interdiffusion in silicate garnets

Ca-(Fe,Mg) interdiffusion experiments between natural single crystals of grossular (Ca_2.74Mg_0.15 Fe_0.23Al_1.76Cr_0.04Si_3.05O₁₂) and almandine (Ca_0.21Mg_0.40 Fe_2.23Mn_0.13Al_2.00Cr_0.08Si_2.99O₁₂ or Ca_0.43Mg_0.36Fe_2.11 Al_1.95Si_3.04O₁₂), were undertaken at 900–1100 °C and 30 kbar, and pressures of 15.0–32.5 kbar at 1000 °C. Samples were buffered by Fe/FeO in most cases. Diffusion profiles were determined by electron microprobe. Across the experimental couples the interdiffusion coefficients (D˜) were almost independent of composition. The diffusion rates in an unbuffered sample were significantly faster than in buffered samples. The temperature dependence of the D˜ (Ca-Fe,Mg) interdiffusion coefficients may be described by