A garnet–hornblende geothermometer: calibration, testing, and application to the Pelona Schist, Southern California

Abstract A garnet–hornblende Fe–Mg exchange geothermometer has been calibrated against the garnet–clinopyroxene geothermometer of Ellis & Green (1979) using data on coexisting garnet + hornblende + clinopyroxene in amphibolite and granulite facies metamorphic assemblages. Data for the Fe–Mg exchange reaction between garnet and hornblende have been fitted to the equation. In K_D=Δ (X_Ca,g) where K_D is the Fe–Mg distribution coefficient, using a robust regression approach, giving a thermometer of the form: with very satisfactory agreement between garnet–hornblende and garnet–clinopyroxene temperatures. The thermometer is applicable below about 850°C to rocks with Mn-poor garnet and common hornblende of widely varying chemistry metamorphosed at low a_O2. Application of the garnet–hornblende geothermometer to Dalradian garnet amphibolites gives temperatures in good agreement with those predicted by pelite petrogenetic grids, ranging from 520°C for the lower garnet zone to 565–610°C for the staurolite to kyanite zones. These results suggest that systematic errors introduced by closure temperature problems in the application of the garnet–clinopyroxene geothermometer to the ‘calibration’data set are not serious. Application to ‘eclogitic’garnet amphibolites suggests that garnet and hornblende seldom attain Fe–Mg exchange equilibrium in these rocks. Quartzo-feldspathic and mafic schists of the Pelona Schist on Sierra Pelona, Southern California, were metamorphosed under high pressure greenschist, epidote–amphibolite and (oligoclase) amphibolite facies beneath the Vincent Thrust at pressures deduced to be 10±1 kbar using the phengite geobarometer, and 8–9kbar using the jadeite content of clinopyroxene in equilibrium with oligoclase and quartz. Application of the garnet–hornblende thermometer gives temperatures ranging from about 480°C at the garnet isograd through 570°C at the oligoclase isograd to a maximum of 620–650°C near the thrust. Inverted thermal gradients beneath the Vincent Thrust were in the range 170 to 250°C per km close to the thrust.     

Late‐stage orogenic loading revealed by contact metamorphism in the northern Appalachians,New York

Pelitic schists from contact aureoles surrounding mafic–ultramafic plutons in Westchester County, NY record a high‐P (~0.8 GPa) high‐T (~790 °C) contact overprint on a Taconic regional metamorphic assemblage (~0.5 GPa). The contact metamorphic assemblage of a pelitic sample in the innermost aureole of the Croton Falls pluton, a small (<10 km²) gabbroic body, consists of quartz–plagioclase–biotite–garnet–sillimanite–ilmenite–graphite–Zn‐rich Al‐spinel. Both K‐feldspar and muscovite are absent, and abundant biotite, plagioclase, sillimanite, quartz and ilmenite inclusions are found within subhedral garnet crystals. Unusually low bulk‐rock Na and K contents imply depletion of alkalic components and silica through anatexis and melt extraction during contact heating relative to typical metapelites outside the aureole. Thermobarometry on nearby samples lacking a contact overprint yields 620–640 °C and 0.5–0.6 GPa. In the aureole sample, WDS X‐ray chemical maps show distinct Ca‐enriched rims on both garnet and matrix plagioclase. Furthermore, biotite inclusions within garnet have significantly higher Mg concentration than matrix biotite. Thermobarometry using GASP and garnet–biotite Mg–Fe exchange equilibria on inclusions and adjacent garnet host interior to the high‐Ca rim zone yield ~0.5 ± 0.1 GPa and ~620 ± 50 °C. Pairs in the modified garnet rim zone yield ~0.9 ± 0.1 GPa and ~790 ± 50 °C. Thermocalc average P–T calculations yield similar results for core (~0.5 ± ~0.1 GPa, ~640 ± ~80 °C) and rim (~0.9 ± ~0.1 GPa, ~800 ± ~90 °C) equilibria. The core assemblages are interpreted to record the P–T conditions of peak metamorphism during the Taconic regional event whereas the rim compositions and matrix assemblages are interpreted to record the P–T conditions during the contact event. The high pressures deduced for this later event are interpreted to reflect loading due to the emplacement of Taconic allochthons in the northern Appalachians during the waning stages of regional metamorphism (after c. 465 Ma) and before contact metamorphism (c. 435 Ma). In the absence of contact metamorphism‐induced recrystallization, it is likely that this regional‐scale loading would remain cryptic or unrecorded.     

Titanium‐in‐biotite thermometry in porphyry copper systems: Challenges to application of the thermometer

Empirical geothermometer dealing with Ti solubility in the Fe‐Mg biotites was originally proposed for biotites in graphitic, peraluminous metapelites containing ilmenite or rutile that equilibrated roughly at 4–6 kbar. Given that biotites are abundant in the porphyry copper systems, this geothermometer has frequently been used for the determination of magmatic–hydrothermal temperatures in the porphyry copper systems. Common associations of porphyry copper deposits (PCDs), that is, low Al content of biotite, biotite chloritization (causes the biotite to become more magnesian and to lose Ti), and biotite formation by amphibole replacement, as well as disequilibrium, local equilibrium, or re‐equilibration of biotites, especially through potassic alteration, may provide significant uncertainty in the temperatures estimated a by Ti‐in‐biotite geothermometer. In addition, besides the calibration range of thermometer for pressure (400–600 MPa), the temperatures of major sulfide precipitation in PCDs (>~400°C) does not fit with the temperature range of thermometer calibration (480–800°C). Worth noting, as confirmed by fluid inclusion data in the Sarkuh PCD, regardless of presence of mineralogical requirements, obtained temperatures of sulfide mineralization using Ti in biotite thermometer could be overestimated. This may be due to the difference between general conditions of sulfide mineralization and calibration range of Ti in the biotite thermometer for pressure and temperature, as well as the metaluminous nature of biotites in PCDs.     

Prograde and retrograde history of eclogites from the Eastern Blue Ridge, North Carolina, USA

Abstract The prograde metamorphism of eclogites is typically obscured by chemical equilibration at peak conditions and by partial requilibration during retrograde metamorphism. Eclogites from the Eastern Blue Ridge of North Carolina retain evidence of their prograde path in the form of inclusions preserved in garnet. These eclogites, from the vicinity of Bakersville, North Carolina, USA are primarily comprised of garnet–clinopyroxene–rutile–hornblende–plagioclase–quartz. Quartz, clinopyroxene, hornblende, rutile, epidote, titanite and biotite are found as inclusions in garnet cores. Included hornblende and clinopyroxene are chemically distinct from their matrix counterparts. Thermobarometry of inclusion sets from different garnets record different conditions. Inclusions of clinozoisite, titanite, rutile and quartz (clinozoisite + titanite = grossular + rutile + quartz + H₂O) yield pressures (6–10 kbar, 400–600 °C and 8–12 kbar 450–680 °C) at or below the minimum peak conditions from matrix phases (10–13 kbar at 600–800 °C). Inclusions of hornblende, biotite and quartz give higher pressures (13–16 kbar and 630–660 °C). Early matrix pyroxene is partially or fully broken down to a diopside–plagioclase symplectite, and both garnet and pyroxene are rimmed with plagioclase and hornblende. Hypersthene is found as a minor phase in some diopside + plagioclase symplectites, which suggests retrogression through the granulite facies. Two‐pyroxene thermometry of this assemblage gives a temperature of c. 750 °C. Pairing the most Mg‐rich garnet composition with the assemblage plagioclase–diopside–hypersthene–quartz gives pressures of 14–16 kbar at this temperature. The hornblende–plagioclase–garnet rim–quartz assemblage yields 9–12 kbar and 500–550 °C. The combined P–T data show a clockwise loop from the amphibolite to eclogite to granulite facies, all of which are overprinted by a texturally late amphibolite facies assemblage. This loop provides an unusually complete P–T history of an eclogite, recording events during and following subduction and continental collision in the early Palaeozoic.     

Calcite–graphite isotope thermometry in amphibolite facies marble, Bancroft, Ontario

This study presents calcite–graphite carbon isotope fractionations for 32 samples from marble in the northern Elzevir terrane of the Central Metasedimentary Belt, Grenville Province, southern Ontario, Canada. These results are compared with temperatures calculated by calcite–dolomite thermometry (15 samples), garnet–biotite thermometry (four samples) and garnet–hornblende thermometry (three samples). Δ_cal‐gr values vary regularly across the area from >6.5‰ in the south to 4.0‰ in the north, which corresponds to temperatures of 525 °C in the south to 650 °C in the north. Previous empirical calibration of the calcite–graphite thermometer agrees very well with calcite–dolomite, garnet–biotite and garnet–hornblende thermometry, whereas, theoretical calibrations compare less well with the independent thermometry. Isograds in marble based on the reactions rutile + calcite + quartz =titanite and tremolite + calcite + quartz = diopside, span temperatures of 525–600 °C and are consistent with calculated temperature–X(CO₂) relations. Results of this study compare favourably with large‐scale regional isotherms, however, local variation is greater than that revealed by large‐scale sampling strategies. It remains unclear whether the temperature–Δ_cal‐gr relationship observed in natural materials below 650 °C represents equilibrium fractionations or not, but the regularity and consistency apparent in this study demonstrate its utility for thermometry in amphibolite facies marble.     

Metamorphic history of eclogites and country rock gneisses in the Aktyuz area,Northern Tien‐Shan,Kyrgyzstan: a record from initiation of subduction through to oceanic closure by continent–continent collision

Eclogites and related high‐P metamorphic rocks occur in the Zaili Range of the Northern Kyrgyz Tien‐Shan (Tianshan) Mountains, which are located in the south‐western segment of the Central Asian Orogenic Belt. Eclogites are preserved in the cores of garnet amphibolites and amphibolites that occur in the Aktyuz area as boudins and layers (up to 2000 m in length) within country rock gneisses. The textures and mineral chemistry of the Aktyuz eclogites, garnet amphibolites and country rock gneisses record three distinct metamorphic events (M1–M3). In the eclogites, the first MP–HT metamorphic event (M1) of amphibolite/epidote‐amphibolite facies conditions (560–650 °C, 4–10 kbar) is established from relict mineral assemblages of polyphase inclusions in the cores and mantles of garnet, i.e. Mg‐taramite + Fe‐staurolite + paragonite ± oligoclase (An_<16) ± hematite. The eclogites also record the second HP‐LT metamorphism (M2) with a prograde stage passing through epidote‐blueschist facies conditions (330–570 °C, 8–16 kbar) to peak metamorphism in the eclogite facies (550–660 °C, 21–23 kbar) and subsequent retrograde metamorphism to epidote‐amphibolite facies conditions (545–565 °C and 10–11 kbar) that defines a clockwise P–T path. thermocalc (average P–T mode) calculations and other geothermobarometers have been applied for the estimation of P–T conditions. M3 is inferred from the garnet amphibolites and country rock gneisses. Garnet amphibolites that underwent this pervasive HP–HT metamorphism after the eclogite facies equilibrium have a peak metamorphic assemblage of garnet and pargasite. The prograde and peak metamorphic conditions of the garnet amphibolites are estimated to be 600–640 °C; 11–12 kbar and 675–735 °C and 14–15 kbar, respectively. Inclusion phases in porphyroblastic plagioclase in the country rock gneisses suggest a prograde stage of the epidote‐amphibolite facies (477 °C and 10 kbar). The peak mineral assemblage of the country rock gneisses of garnet, plagioclase (An_11–16), phengite, biotite, quartz and rutile indicate 635–745 °C and 13–15 kbar. The P–T conditions estimated for the prograde, peak and retrograde stages in garnet amphibolite and country rock are similar, implying that the third metamorphic event in the garnet amphibolites was correlated with the metamorphism in the country rock gneisses. The eclogites also show evidence of the third metamorphic event with development of the prograde mineral assemblage pargasite, oligoclase and biotite after the retrograde epidote‐amphibolite facies metamorphism. The three metamorphic events occurred in distinct tectonic settings: (i) metamorphism along the hot hangingwall at the inception of subduction, (ii) subsequent subduction zone metamorphism of the oceanic plate and exhumation, and (iii) continent–continent collision and exhumation of the entire metamorphic sequences. These tectonic processes document the initial stage of closure of a palaeo‐ocean subduction to its completion by continent–continent collision.     

Triassic eclogite from northern Vietnam: inferences and geological significance

T he first finding of low‐temperature eclogites from the Indochina region is reported. The eclogites occur along the Song Ma Suture zone in northern Vietnam, which is widely regarded as the boundary between the South China and Indochina cratons. The major lithology of the area is pelitic schist that contains garnet and phengite with or without biotite, chloritoid, staurolite and kyanite, and which encloses blocks and lenses of eclogite and amphibolite. The eclogites commonly consist of garnet, omphacite, phengite, rutile, quartz and/or epidote with secondary barroisite. Omphacite is commonly surrounded by a symplectite of Na‐poor omphacite and Na‐rich plagioclase. In highly retrograded domains, diopside + tremolite + plagioclase symplectites replace the primary phases. Estimated peak‐pressure metamorphic conditions based on isochemical phase diagrams for the eclogites are 2.1–2.2 GPa and 600–620 °C, even though thermobarometric results yield higher pressure and temperature conditions (2.6–2.8 GPa and 620–680 °C). The eclogites underwent a clockwise P–T trajectory with a post‐peak‐pressure increase of temperature to a maximum of >750 °C at 1.7 GPa and a subsequent cooling during decompression to 650 °C and 1.3 GPa, which was followed by additional cooling before close‐to‐isothermal decompression to ∼530 °C at 0.5 GPa. The surrounding pelitic schist (garnet–chloritoid–phengite) records similar metamorphic conditions (580–600 °C at 1.9–2.3 GPa) and a monazite chemical age of 243 ± 4 Ma. A few monazite inclusions within garnet and the cores of some zoned monazite in garnet–phengite schist record an older thermal event (424 ± 15 Ma). The present results indicate that the Indochina craton was deeply (>70 km) subducted beneath the South China craton in the Triassic. The Silurian cores of monazite grains may relate to an older non‐collisional event in the Indochina craton.     

On the interpretation of peak metamorphic temperatures in light of garnet diffusion during cooling

Abstract Finite difference models of Fe-Mg diffusion in garnet undergoing cooling from metamorphic peak conditions are used to infer the significance of temperatures calculated using garnet-biotite Fe-Mg exchange thermometry. For rocks cooled from high grades where the garnet was initially homogeneous, the calculated temperature (T_calc) using garnet core and matrix biotite depends on the size of the garnet, the ratio of garnet to biotite in the rock (V_garnet/V_biotite) and the cooling rate. For garnets with radii of 1 mm and V_garnet/V_biotite<1, T_calc is 633, 700 and 777°C for cooling rates of 1, 10 and 100°C/Ma. For V_garnet/V_biotite= 1 and 4 and a cooling rate of 10° C/Ma, T_calc is approximately 660 and 610° C, respectively. Smaller and larger garnets have lower and higher T_calc, respectively. These results suggest that peak metamorphic temperatures may be reliably attained from rocks crystallized at conditions below T_calc of the garnet core, provided that V_garnet/V_biotite is sufficiently small (<0.1) and that the composition of the biotite at the metamorphic peak has not been altered during cooling. Numerical experiments on amphibolite facies garnets with nominal peak temperatures of 550–600° C generate a ‘well’in Fe/(Fe + Mg) near the rim during cooling. Maximum calculated temperatures for the assemblage garnet + chlorite + biotite + muscovite + plagioclase + quartz using the Fe/(Fe + Mg) at the bottom of the ‘well’with matrix biotite range from 23–43° C to 5–12° C below the peak metamorphic temperature for cooling rates of 1 and 100° C/Ma, respectively. Maximum calculated temperatures for the assemblage garnet + staurolite + biotite + muscovite + plagioclase + quartz are approximately 70° C below the peak metamorphic temperature and are not strongly dependent on cooling rate. The results of this study indicate that it may be very difficult to calculate peak metamorphic temperatures using garnet-biotite Fe-Mg exchange thermometry on amphibolite facies rocks (T_max > 550° C) because the rim composition of the garnet, which is required to calculate the peak temperature, is that most easily destroyed by diffusion.     

Empirical garnet–muscovite geothermometry in low-grade metapelites, Selwyn Range (Canadian Rockies)

Abstract Partitioning of Fe and Mg between garnet and phengitic muscovite was calibrated as a geothermometer by Green & Hellman (1982) using experimental data at 25–30 kbar. When the thermometer is applied to pelites regionally metamorphosed at pressures of between 3 and 7 kbar it yields temperatures much higher than those from the garnet–biotite thermometer. A new empirical calibration is proposed for use with such rocks, with particular application where garnet occurs at lower grades than biotite. The new calibration is where K is given by: In K = In K _d and X _ii are mole fractions in the garnets.
The calibration was derived from comparison with the garnet–biotite thermometer of Ferry & Spear (1978), assuming no pressure-dependence for the partitioning between garnet and muscovite, no ferric iron partitioning, ideal mixing in muscovite, and the garnet mixing model of Ganguly & Saxena (1984) modified for a non-linear Ca effect. This latter garnet mixing model was selected because it gave the geologically most reasonable results. It has not proved possible to distinguish a pressure effect from a ferric-iron effect.
Despite the simplifying assumptions used to derive the calibration, it yields temperatures generally within 15°C of those given by the garnet–biotite thermometer, and has been used to supply thermometric data in a low-grade region of the Canadian Rockies.     

Constraining the P–T path of a MORB-type eclogite using pseudosections, garnet zoning and garnet-clinopyroxene thermometry: an example from the Bohemian Massif

A mid‐ocean ridge basalt (MORB)‐type eclogite from the Moldanubian domain in the Bohemian Massif retains evidence of its prograde path in the form of inclusions of hornblende, plagioclase, clinopyroxene, titanite, ilmenite and rutile preserved in zoned garnet. Prograde zoning involves a flat grossular core followed by a grossular spike and decrease at the rim, whereas Fe/(Fe + Mg) is also flat in the core and then decreases at the rim. In a pseudosection for H₂O‐saturated conditions, garnet with such a zoning grows along an isothermal burial path at c. 750 °C from 10 kbar in the assemblage plagioclase‐hornblende‐diopsidic clinopyroxene‐quartz, then in hornblende‐diopsidic clinopyroxene‐quartz, and ends its growth at 17–18 kbar. From this point, there is no pseudosection‐based information on further increase in pressure or temperature. Then, with garnet‐clinopyroxene thermometry, the focus is on the dependence on, and the uncertainties stemming from the unknown Fe³⁺ content in clinopyroxene. Assuming no Fe³⁺ in the clinopyroxene gives a serious and unwarranted upward bias to calculated temperatures. A Fe³⁺‐contributed uncertainty of ±40 °C combined with a calibration and other uncertainties gives a peak temperature of 760 ± 90 °C at 18 kbar, consistent with no further heating following burial to eclogite facies conditions. Further pseudosection modelling suggests that decompression to c. 12 kbar occurred essentially isothermally from the metamorphic peak under H₂O‐undersaturated conditions (c. 1.3 mol.% H₂O) that allowed the preservation of the majority of garnet with symplectitic as well as relict clinopyroxene. The modelling also shows that a MORB‐type eclogite decompressed to c. 8 kbar ends as an amphibolite if it is H₂O saturated, but if it is H₂O‐undersaturated it contains assemblages with orthopyroxene. Increasing H₂O undersaturation causes an earlier transition to SiO₂ undersaturation on decompression, leading to the appearance of spinel‐bearing assemblages. Granulite facies‐looking overprints of eclogites may develop at amphibolite facies conditions.     

Recalibration of mutually consistent garnet–biotite and garnet–cordierite geothermometers

Garnet–biotite and garnet–cordierite geothermometers have been consistently calibrated, using the results of Fe²⁺–Mg cation exchange experiments and utilizing recently evaluated nonideal mixing properties of garnet. Nonideal mixing parameters of biotite (including Fe, Mg, Al^VI, and Ti) and of cordierite (involving Fe and Mg) are evaluated in terms of iterative multiple least-square regressions of the experimental results. Assuming the presence of ferric Fe in biotite in relation to the coexisting Fe-oxide phases (Case A), and assuming the absence of ferric Fe in biotite (Case B), two formulae of garnet–biotite thermometer have been derived. The garnet–cordierite geothermometer was constructed using Margules parameters of garnet adopted in the garnet–biotite geothermometers. The newly calibrated garnet–biotite and garnet–cordierite thermometers clearly show improved conformity in the calculated temperatures. The thermometers give temperatures that are consistent with each other using natural garnet–biotite–cordierite assemblages within ±50 °C. The effects of ferric Fe in biotite on garnet–biotite thermometry have been evaluated comparing the two calibrations of the thermometer. The effects are significant; it is clarified that taking ferric Fe content in biotite into account leads to less dispersion of thermometric results.     

Assessment of the Garnet-Clinopyroxene Thermometer

A thermometer based on the MgFe_?1 exchange equilibrium between garnet and clinopyroxene is formulated by using new experimental data measured at 600° to 950°C, 0.8 to 3.0 GPa, and f(O₂) defined by the fayalite-quartz-magnetite buffer in the basalt-H₂O system. The new formulation is T = 3820 / 1.828 + lnK_D (1 + a(2.2 ? p)), where T is temperature (K), P is pressure (GPa), KD is the Fe-Mg partition coefficient between garnet and clino-pyroxene, defined as KD = (Fe²+/Mg)garnet/(Fe²+/Mg) clinopyroxene, and a = 132/T. Application of the thermometer to rocks in amphibolite, granulite, and eclogite terranes yields temperatures that are in reasonable agreement with other well-calibrated thermometers and the experimental calibrations by Ellis and Green (1979) and Pattison and Newton (1989).     

Calibration of the garnet–biotite–Al2SiO5–quartz geobarometer for metapelites

A garnet–biotite–Al₂SiO₅–quartz (GBAQ) geobarometer was empirically calibrated using more than 700 natural metapelites with a broad compositional range of garnet and biotite under P–T conditions of 450–950°C and 1–17 kbar. In the calibration, activity models of garnet and biotite identical to those in the garnet–biotite (GB) geothermometer of Holdaway [American Mineralogist 2000, 85: 881–892] were used. Therefore, the GBAQ geobarometer and the GB geothermometer can be simultaneously applied to iteratively estimate metamorphic P–T conditions. Successful applications of the GBAQ geobarometer to natural metapelites certify its validity. Most importantly, when plagioclase is absent or CaO components in garnet and/or plagioclase are deficient, this geobarometer may prove useful for estimating metamorphic pressures. The random error of the present GBAQ geobarometer is inferred to be around ±1.8 kbar. An electronic spreadsheet is available as Table S4 to apply the GBAQ geobarometer in combination with the GB geothermometer.     

Metamorphic differentiation at Einasleigh,Northern Queensland

Biotite‐muscovite‐garnet gneisses at Einasleigh contain quartz‐feldspar veins composed of the same minerals as found in the enclosing rock. The vein‐gneiss boundaries are commonly irregular and on a microscopic scale, gradational.

Certain amphibolite layers contain quartz‐feldspar veins composed of the same minerals as found in the amphibolite. Hornblende‐rich extraction zones surround these veins, and material balance calculations show that all or nearly all of the vein‐forming matter was locally derived. Variation in the abundance of hornblende and plagioclase in the amphibolite as a function of distance from a quartz‐feldspar vein can be expressed by error‐function curves, thus suggesting that the mineral‐segregation process was diffusion‐controlled. During the mineral rearrangement, the Na and Ca contents of plagioclase have evidently remained unchanged, but the vein hornblende has become slightly richer in Fe+3, Mg, and Ca, and poorer in Si and Al relative to hornblende in the adjacent amphibolite.

A certain biotite‐plagioclase rock forms layers and boudins in the gneisses and contains pegmatite veins composed of the same minerals as found in the host rock. The plagioclase in these veins is more sodic than that in the host rock while the biotite contains slightly more Ti and Fe+² and less Si and Mg than the biotite of the enclosing rock.

The data indicate that significant portions of the vein‐forming matter at Einasleigh were locally derived. The chemistry of some minerals has changed slightly during the segregation process, resulting possibly from different diffusion rates for the different mineral‐forming constituents.     

Petrogenetic significance of orthopyroxene-free garnet + clinopyroxene + plagioclase ± quartz-bearing metabasites with respect to the amphibolite and granulite facies

Orthopyroxene‐free garnet + clinopyroxene + plagioclase ± quartz‐bearing mineral assemblages represent the paragenetic link between plagioclase‐free eclogite facies metabasites and orthopyroxene‐bearing granulite facies metabasites. Although these assemblages are most commonly developed under P–T conditions consistent with high pressure granulite facies, they sometimes occur at lower grade in the amphibolite facies. Thus, these assemblages are characteristic but not definitive of high pressure granulite facies. Compositional factors favouring their development at amphibolite grade include Fe‐rich mineral compositions, Ca‐rich garnet and plagioclase, and Ti‐poor hornblende. The generalized reaction that accounts for the prograde development of garnet + clinopyroxene + plagioclase ± quartz from a hornblende + plagioclase + quartz‐bearing (amphibolite) precursor is Hbl + Pl + Qtz=Grt + Cpx + liquid or vapour, depending on whether the reaction occurs above or below the solidus. There are significant discrepancies between experimental and natural constraints on the P–T conditions of orthopyroxene‐free garnet + clinopyroxene + plagioclase ± quartz‐bearing mineral assemblages and therefore on the P–T position of this reaction. Semi‐quantitative thermodynamic modelling of this reaction is hampered by the lack of a melt model and gives results that are only moderately successful in rationalizing the natural and experimental data.     

Petrogenetic relations among titanium‐rich minerals in an anatectic high‐P mafic granulite

The petrogenetic relations among Ti‐rich minerals in high‐grade metabasites is illuminated here through a detailed petrological investigation of an anatectic garnet–clinopyroxene granulite from the Grenville Province, Ontario, Canada containing rutile, titanite and ilmenite in distinct microtextural settings. Garnet porphyroblasts exhibit zoned Ti concentrations (up to 0.15 wt% TiO₂ in their cores), as well as a variety of rutile inclusion types, including clusters of small, variably elongate grains and thin (≤1 μm) oriented needles. Calcite inclusions in garnet, commonly observed surrounding garnet cores containing quartz and clinozoisite, indicate the presence of evolving C–O–H fluids during garnet growth and suggest that the rutile clusters may have formed from subsequent Ti diffusion and rutile precipitation within existing fluid inclusions. Titanite forms large subhedral crystals and typically occurs where the primary garnet–clinopyroxene assemblage is in contact with leucosome containing megacrystic hornblende, silvialitic scapolite and calcic plagioclase. Many titanite crystals exhibit marginal subgrains that correspond with sharp changes in their major and trace element composition, likely related to a dissolution–precipitation or recrystallization process following primary crystallization. Clinopyroxene–ilmenite symplectite coronas surround titanite in most locations, likely forming from reaction with the hornblende‐plagioclase matrix (±fluids/melt). Integration of multi‐equilibria thermobarometry and Zr thermometry in rutile and titanite with phase equilibrium modelling allows definition of a clockwise P–T path evolving to peak pressures of ~1.5 GPa at ~750°C during garnet and rutile growth, followed by peak temperature conditions of ~1.2 GPa and ~820–880°C associated with melt‐present titanite growth, and finally cooling and decompression to regional amphibolite facies conditions (~1.0 GPa and ~750°C) associated with the formation of clinopyroxene–ilmenite symplectites surrounding titanite. P–T pseudosections calculated for the pristine (leucosome‐ and titanite ‐free) metabasite bulk composition reproduce much of the prograde phase relations, but predict rutile as the stable Ti‐rich mineral at the peak thermal conditions associated with melt‐present titanite growth. The P–M(CaO) and T–M(CaO) models show that bulk CaO concentrations have a significant effect on the stability ranges of titanite and rutile. Increased bulk CaO tends to stabilize titanite to higher pressure and temperature at the expense of rutile, with a ≥15% increase in CaO producing the observed titanite‐bearing assemblage at high‐P granulite facies conditions. Thus, the model results are consistent with the textural observations, which suggest that titanite stability is associated with a chemical exchange between the host metabasite and a Ca‐rich melt.     

Metabasites with eclogite facies relics from Variscides in Sardinia,Italy: a review

Metabasites with eclogite facies relics occur in northern Sardinia as massive to strongly foliated lenses or boudins embedded within low- to medium-grade rocks (Anglona) and migmatites (NE Sardinia). U–Pb zircon dating yielded 453 ± 14, 457 ± 2 and 460 ± 5 Ma as the protolith ages; 400 ± 10 and 403 ± 4 Ma have been interpreted as the ages of the HP event and 352 ± 3 and 327 ± 7 Ma as the ages of the main Variscan retrograde events. A pre-eclogite stage is documented by the occurrence of tschermakite, zoisite relics within garnet porphyroblasts (Punta de li Tulchi) and an edenite–andesine inclusion within a relict kyanite porphyroblast (Golfo Aranci). Four main metamorphic stages have been distinguished in the eclogite evolution: (1) eclogite stage, revealed by the occurrence of armoured omphacite relics within garnet porphyroblasts. The Golfo Aranci eclogites also include kyanite, Mg-rich garnet and pargasite; (2) granulite stage, producing orthopyroxene and clinopyroxene–plagioclase symplectites replacing omphacite. At Golfo Aranci, the symplectitic rims around relict kyanite consist of sapphirine, anorthite, corundum and spinel; (3) amphibolite stage, leading to the formation of amphibole–plagioclase kelyphites between garnet porphyroblasts and pyroxene–plagioclase symplectites and to the growth of cummingtonite on orthopyroxene. Tschermakite to Mg-hornblende, plagioclase, cummingtonite, ilmenite, titanite and biotite are coexisting phases; (4) greenschist to sub-greenschist stage, defined by the appearance of actinolite, chlorite, epidote ss, titanite, sericite and prehnite. The following P–T ranges have been estimated for the different stages. Eclogite stage 550–700°C; 1.3–1.7 GPa; granulite stage 650–900°C; 0.8–1.2 GPa, clustering in the range 1.0–1.2 GPa; amphibolite stage 550–740°C; 0.3–0.7 GPa; greenschist stage 300–400°C; 0.2–0.3 GPa. Comparable ranges characterise the other Variscan massifs in Europe; eclogite stage: T = 530–800°C; P from 0.7–1.1 to 1.7 ± 0.3 GPa; granulite stage T = 760–870°C and P from 1.1–1.4 to 7.2–9.9 GPa, clustering around 1.0–1.2 GPa. Whole-rock chemistry: Sardinian eclogites are N- to T-MORB; European ones N- to E-MORB or calc-alkaline.     

Metamorphism of the Basement of the Qilian Fold Belt in the Minhe-Ledu Area, Qinghai Province, NW China

The basement of the central Qilian fold belt exposed along the Minhe-Ledu highway consists of psammitic schists, metabasitic rocks, and crystalline limestone. Migmatitic rocks occur sporadically among psammitic schist and metabasitic rocks. The mineral assemblage of psammitic schist is muscovite + biotite + feldspar + quartz ± tourmaline ± titanite ± sillimanite and that of metabasitic rocks is amphibole + plagioclase + biotite ± apatite ± magnetite ± pyroxene ± garnet ± quartz. The migmatitic rock consists of leucosome and restite of various volume proportions; the former consists of muscovite + alkaline feldspar + quartz ± garnet ± plagioclase while the latter is either fragments of psammitic schist or those of metabasitic rock. The crystalline limestone consists of calcite that has been partly replaced by olivine. The olivine was subsequently altered to serpentine. Weak deformations as indicated by cleavages and fractures were imposed prominently on the psammitic schists, occasionally on me     

Hydrothermal clinopyroxenes of the Skaergaard intrusion

Magmatic augites reacted with high temperature aqueous solutions to form secondary calcic pyroxenes during the subsolidus cooling of the Skaergaard intrusion. Secondary, hydrothermal clinopyroxenes replace wall rock igneous augites at the margins of veins filled with calcic amphibole. These veins are up to several millimeters wide and tens of meters in length. Hydrothermal clinopyroxenes are a ubiquitous and characteristic phase in the earliest veins throughout the Layered Series of the intrusion, and occur rarely in late veins that, in some places, crosscut the early veins. Associated secondary phases in early veins include amphiboles ranging in composition from actinolite to hornblende, together with biotite, Fe-Ti oxides and calcic plagioclase. Hydrothermal clinopyroxenes in late veins may be associated with actinolite, hornblende, biotite, magnetite and albite.Hydrothermal clinopyroxenes are depleted in Fe, Mg and minor elements, and enriched in Ca and Si relative to igneous augites in the Layered Series gabbros. Secondary vein pyroxenes are similar in composition to calcic pyroxenes from amphibolite facies metamorphic rocks. Clinopyroxene solvus thermometry suggests minimum temperatures of equilibration of between 500° and 750° C. These temperatures, combined with numerical transport models of the intrusion, suggest that vein clinopyroxenes could have formed during 20,000 to 60,000 year time intervals associated with a maximum in the fluid flux through fractures in the Layered Series.     

Mineral reactions participating in intragranular fracture propagation: implications for stress corrosion cracking

Two examples of mineral reactions accompanying intragranular fracturing of silicates are described from amphibolites at the Grenville front, Coniston, Ontario, and a granodiorite within the Miéville shear zone, Switzerland. At these localities coarse grained (> 1 mm) hornblende and biotite respectively have undergone initial deformation by intense transgranular fracturing. The ambient temperature of deformation is estimated at 400–500°C for the amphibolites, and 250–300°C for the granodiorite.Fracture intensity within hornblende increases with progressive deformation until fractures coalesce and grains lose cohesion. Fractures are occupied by hornblende in close optical continuity with the parent grain, and typically contain median sutures decorated by arrays of solid inclusions. Relative to the parent grain, hornblende in fractures is depleted in Ti, Al, plus K, and enriched in Mg. Given the preferential partitioning of Mg, Al^VI and Ti into the M2 site of calcic amphiboles, the decrease of Ti and Al^VI in the host-to-crack transition is consistent with the corresponding increase of the Mg/(Mg + Fe²⁺) ratio.Fractures within biotite are bounded by an envelope of paler brown biotite which corresponds to a decrease of Ti and increase of Fe + Mg relative to regions unaffected by cracking. Fractures are occupied by secondary ilmenite, low-Ti biotite and high-Ti muscovite. Ti and Al do not vary significantly as a function of Mg/(Fe + Mg) in the host-to-crack transition, as anticipated from the approximately equal partitioning of these two cations into the M1 and M2 octahedral cation sites. The direct relationship of the mineral reactions to the fractures is taken as evidence for the participation of the reactions in crack propagation. These features may thus represent examples of natural stress corrosion cracking.