Dislocation structures in pyropes from Norwegian and Czech garnet peridotites

The dislocation structures of minerals may give important information on the deformational history of rocks. Dislocations in pyrope-rich garnets are revealed by etching in hydrofluoric acid. Pyropes from Norwegian and Czech garnet peridotites characteristically display tangled arrangements and cell structures similar to those formed in metals and alloys in creep.Publication no. 7 in the Norwegian Geotraverse Project.     

Chronology of the high-pressure metamorphism of Norwegian garnet peridotites/pyroxenites

Eclogite facies mineral assemblages are variably preserved in mafic and ultramafic rocks within the Western Gneiss Region (WGR) of Norway. Mineralogical and microstructural data indicate that some Mg–Cr-rich, Alpine-type peridotites have had a complex metamorphic history. The metamorphic evolution of these rocks has been described in terms of a seven-stage evolutionary model; each stage is characterized by a specific mineral assemblage. Stages II and III both comprise garnet-bearing mineral assemblages. Garnet-bearing assemblages are also present in Fe–Ti-rich peridotites which commonly occur as layers in mafic complexes. Sm–Nd isotopic results are reported for mineral and whole rock samples from both of these types of peridotites and related rocks. The partitioning of Sm and Nd between coexisting garnet and clinopyroxene is used to assess chemical equilibrium. One sample of Mg–Cr-type peridotite shows non-disturbed partitioning of Sm and Nd between Stage II garnet and clinopyroxene pairs and yields a garnet–clinopyroxene–whole-rock date of 1703 ± 29 Ma (I= 0.51069, MSWD = 0.04). This is the best estimate for the age of the Stage II high-P assemblage. Other Stage II garnet–clinopyroxene pairs reflect later disturbance of the Sm–Nd system and yield dates in the range 1303 to 1040 Ma. These dates may not have any geological significance. Stage III garnet–clinopyroxene pairs typically have equilibrated Sm–Nd partitioning and two samples yield dates of 437 ± 58 and 511 ± 18 Ma. This suggests that equilibration of the Stage III high-P assemblage is related to the Caledonian orogeny and is more or less contemporaneous with high-P metamorphism of ‘country-rock’eclogites in the surrounding gneisses. The Sm–Nd mineral data for the Fe–Ti-rich garnet peridotites and for a superferrian eclogite, which occurs as a dyke within the Gurskebotn Mg–Cr-type peridotite, are consistent with a Palaeozoic high-P metamorphism. Finally a synoptic P–T–t path is proposed for the Mg–Cr-type peridotites which is consistent with the petrological and geochronological data.     

A general model for the intrusion and evolution of 'mantle' garnet peridotites in high-pressure and ultra-high-pressure metamorphic terranes

Garnet‐bearing peridotite lenses are minor but significant components of most metamorphic terranes characterized by high‐temperature eclogite facies assemblages. Most peridotite intrudes when slabs of continental crust are subducted deeply (60–120 km) into the mantle, usually by following oceanic lithosphere down an established subduction zone. Peridotite is transferred from the resulting mantle wedge into the crustal footwall through brittle and/or ductile mechanisms. These ‘mantle’ peridotites vary petrographically, chemically, isotopically, chronologically and thermobarometrically from orogen to orogen, within orogens and even within individual terranes. The variations reflect: (1) derivation from different mantle sources (oceanic or continental lithosphere, asthenosphere); (2) perturbations while the mantle wedges were above subducting oceanic lithosphere; and (3) changes within the host crustal slabs during intrusion, subduction and exhumation. Peridotite caught within mantle wedges above oceanic subduction zones will tend to recrystallize and be contaminated by fluids derived from the subducting oceanic crust. These ‘subduction zone peridotites’ intrude during the subsequent subduction of continental crust. Low‐pressure protoliths introduced at shallow (serpentinite, plagioclase peridotite) and intermediate (spinel peridotite) mantle depths (20–50 km) may be carried to deeper levels within the host slab and undergo high‐pressure metamorphism along with the enclosing rocks. If subducted deeply enough, the peridotites will develop garnet‐bearing assemblages that are isofacial with, and give the same recrystallization ages as, the eclogite facies country rocks. Peridotites introduced at deeper levels (50–120 km) may already contain garnet when they intrude and will not necessarily be isofacial or isochronous with the enclosing crustal rocks. Some garnet peridotites recrystallize from spinel peridotite precursors at very high temperatures (c. 1200 °C) and may derive ultimately from the asthenosphere. Other peridotites are from old (>1 Ga), cold (c. 850 °C), subcontinental mantle (‘relict peridotites’) and seem to require the development of major intra‐cratonic faults to effect their intrusion.     

Deep subduction of mantle-derived garnet peridotites from the Su-Lu UHP metamorphic terrane in China

Garnet peridotites from the southern Su‐Lu ultra‐high‐pressure metamorphic (UHPM) terrane, eastern China, contain porphyroblastic garnet with aligned inclusions comprising a low‐P–T mineral assemblage (chlorite, hornblende, Na‐gedrite, Na‐phlogopite, talc, spinel and pyrite). Orthopyroxene porphyroblasts show fine exsolution lamellae of clinopyroxene and minor chromite. A clinopyroxene inclusion in garnet shows some orthopyroxene exsolution lamellae. Both the rims of porphyroblastic pyroxene and garnet and the matrix pyroxene and garnet crystallized at the expense of olivine. This is interpreted as a result of metasomatism of the peridotites by an SiO₂‐rich melt at UHP conditions. A chromian garnet further overgrew on the rims of the garnet. The X_Mg values (Mg/(Mg+Fe)) of porphyroblastic garnet decrease from core to rim and vary in different peridotite samples, while the compositions of both the porphyroblastic and the matrix pyroxene are similar in terms of Ca–Mg–Fe. The Mg‐rich cores of porphyroblastic garnet and orthopyroxene record high temperatures and pressures (c. 1000 °C, ≥5.1 GPa), whereas the matrix minerals, including the rims of porphyroblasts, record much lower P–T (c. 4.2 GPa, c. 760 °C). Sm–Nd data give apparent isochron ages of c. 380 Ma and negative ε_Nd(0) values (c.?9). These dates are considered meaningless due to isotopic disequilibrium between garnet cores and the rest of the rocks. The isotopic disequilibrium was probably caused by metasomatism of the peridotites by melt/fluids derived from the coevally subducted crustal materials. On the other hand, the Rb–Sr isotopic systems of phlogopite and clinopyroxene appear to have reached equilibrium and record a cooling age of c. 205 Ma. It is suggested that the garnet peridotites were originally emplaced into a low‐P–T environment prior to the c. 220 Ma continental collision, during which they were subducted together with crustal rocks to mantle depth and subjected to UHP metamorphism. An important corollary is that at least some of the coevally subducted crustal rocks in the Su‐Lu terrane have been subjected to peak metamorphism at P–T conditions much higher than presently estimated (≥2.7 GPa, ≤800 °C).     

关于造山带幔源橄榄岩变质演化的一个普遍规律?

来自柴达木盆地北缘、西藏雅鲁藏布江和苏鲁等三个造山带的橄榄岩样品中均存在蛇纹岩矿物被包裹于橄榄岩矿物的现象.包裹体矿物包括利蛇纹石、纤维蛇纹石、叶蛇纹石、磁铁矿、水镁石、斜方和单斜角闪石、绿泥石、滑石、Fe-Ni硫化物、含水钙铬榴石、钙铝榴石、脆云母等,它们指示橄榄岩先从地幔就位于地壳发生蛇纹岩化再经历高压变质作用的过程,记录着岩石圈从裂解到碰撞的演化历史.结合近来国际上出现的类似报道,本文提出这是造山带变质橄榄岩的一个普遍规律.因此,造山带变质橄榄岩的化学组成不同程度地受到地壳物质的混染,不能准确反映原始上地幔的组成.     

Evaluation of thermobarometers for garnet peridotites

The accuracy and precision of a large number of combinations of geothermometers and geo-barometers for garnet lherzolites have been evaluated with a suite of well-equilibrated xenoliths from kimberlites of northern Lesotho. Accuracy was tested by comparison of P-T estimates for a diamond-bearing and a graphite-bearing xenolith with the experimentally determined diamond-graphite univariant curve and by comparison of P-T estimates for phlogopite-bearing xenoliths to the high-temperature stability limit of phlogopite (Eggler and Wendlandt, 1979). Precision was evaluated by measuring the scatter of P-T estimates for each of four xenoliths from a wide range of P and T when many point analyses of the constituent minerals are used for P-T estimation. A thermobarometer composed of the uncorrected diopside-enstatite miscibility gap of Lindsley and Dixon (1976), combined with the uncorrected isopleths for aluminum in enstatite coexisting with pyrope of MacGregor (1974), is most satisfactory. Correction schemes such as those of Wells (1977) and Wood (1974) will ultimately provide a better means of P-T estimation, but at the present stage of development they serve to decrease precision without a demonstrable increase in accuracy. Thermometers based on $\text{Fe}{}^{\mathrm{2+}}\text{Mg}$ exchange reactions are imprecise because of variable and unknown $\text{Fe}{}^{\mathrm{2+}}\text{Fe}{}^{\mathrm{3+}}$ in minerals and xenoliths. The inflection observed in the northern Lesotho paleogeotherm cannot be an artifact of the method of temperature estimation.     

Petrology and P–T evolution of garnet peridotites from central Sulawesi, Indonesia

Alpine‐type orogenic garnet‐bearing peridotites, associated with quartzo‐feldspathic gneisses of a 140–115 Ma high‐pressure/ultra‐high‐pressure metamorphic (HP‐UHPM) terrane, occur in two regions of the Indonesian island of Sulawesi. Both exposures are located within NW–SE‐trending strike–slip fault zones. Garnet lherzolite occurs as <10 m wide fault slices juxtaposed against Miocene granite in the left‐lateral Palu‐Koro (P‐K) fault valley, and as 10–30 m wide, fault‐bounded outcrops juxtaposed against gabbros and peridotites of the East Sulawesi ophiolite within the right‐lateral Ampana fault in the Bongka river (BR) valley. Six evolutionary stages of recrystallization can be recognized in the peridotites from both localities. Stage I, the precursor spinel lherzolite assemblage, is characterized by Ol+Cpx+Opx±Prg‐Amp ± Spl±Rt±Phl, as inclusions within garnet cores. Stage II, the main garnet lherzolite assemblage, consists of coarse‐grained Ol+Opx+Cpx+Grt; whereas finer‐grained, neoblastic Ol+Opx+Grt+Cpx±Spl±Prg‐Amp±Phl constitutes stage III. Stages IV and V are manifest as kelyphites of fibrous Opx+Cpx+Spl in inner coronas, and Opx+Spl+Prg‐Amp±Ep in outer coronas around garnet, respectively. The final (greenschist facies) retrogressive stage VI is accompanied by recrystallization of Serp+Chl±Mag±Tr±Ni sulphides±Tlc±Cal. P–T conditions of the hydrated precursor spinel lherzolite stage I were probably about 750 °C at 15–20 kbar. P–T determinations of the peak stage IIc (from core compositions) display considerable variation for samples derived from different outcrops, with clustering at 26–38 kbar, 1025–1210 °C (P‐K & BR); 19–21 kbar, 1070–1090 °C (P‐K), and 40–48 kbar, 1205–1290 °C (BR). Stage IIr (derived from rim compositions) generally records decompression of around 4–12 kbar accompanied by cooling of 50–240 °C from the IIc peak stage. Stage III, which post‐dates a phase of ductile deformation, yielded 22±2 kbar at 750±25 °C (P‐K) and 16±2 kbar at 730±40 °C (BR). The granulite–amphibolite–greenschist decompression sequence reflects uplift to upper crustal levels from conditions of 647–862 °C at P=15 kbar (stage IV), through 580–635 °C at P=10–12 kbar (stage V) to 350–400 °C at P=4–7 kbar (stage VI), respectively, and is identical to the sequence recorded in associated granulite, gneiss and eclogite. Sulawesi garnet peridotites are interpreted to represent minor components of the extensive HP‐UHP (peak P >28 kbar, peak T of c. 760 °C) metamorphic basement terrane, which was recrystallized and uplifted in a N‐dipping continental collision zone at the southern Sundaland margin in the mid‐Cretaceous. The low‐T , low‐P and metasomatized spinel lherzolite precursor to the garnet lherzolite probably represents mantle wedge rocks that were dragged down parallel to the slab–wedge interface in a subduction/collision zone by induced corner flow. Ductile tectonic incorporation into the underthrust continental crust from various depths along the interface probably occurred during the exhumation stage, and the garnet peridotites were subsequently uplifted within the HP‐UHPM nappe, suffering a similar decompression history to that experienced by the regional schists and gneisses. Final exhumation from upper crustal levels was clearly facilitated by entrainment in Neogene granitic plutons, and/or Oligocene trans‐tension in deep‐seated strike–slip fault zones.     

Internally consistent geothermometers for garnet peridotites and pyroxenites

Mutual relationships among temperatures estimated with the most widely used geothermometers for garnet peridotites and pyroxenites demonstrate that the methods are not internally consistent and may diverge by over 200°C even in well-equilibrated mantle xenoliths. The Taylor (N Jb Min Abh 172:381–408, 1998) two-pyroxene (TA98) and the Nimis and Taylor (Contrib Mineral Petrol 139:541–554, 2000) single-clinopyroxene thermometers are shown to provide the most reliable estimates, as they reproduce the temperatures of experiments in a variety of simple and natural peridotitic systems. Discrepancies between these two thermometers are negligible in applications to a wide variety of natural samples (≤30°C). The Brey and Köhler (J Petrol 31:1353–1378, 1990) Ca-in-Opx thermometer shows good agreement with TA98 in the range 1,000–1,400°C and a positive bias at lower T (up to +90°C, on average, at T _TA98 = 700°C). The popular Brey and Köhler (J Petrol 31:1353–1378, 1990) two-pyroxene thermometer performs well on clinopyroxene with Na contents of ~0.05 atoms per 6-oxygen formula, but shows a systematic positive bias with increasing Na_Cpx (+150°C at Na_Cpx = 0.25). Among Fe–Mg exchange thermometers, the Harley (Contrib Mineral Petrol 86:359–373, 1984) orthopyroxene–garnet and the recent Wu and Zhao (J Metamorphic Geol 25:497–505, 2007) olivine–garnet formulations show the highest precision, but systematically diverge (up to ca. 150°C, on average) from TA98 estimates at T far from 1,100°C and at T < 1,200°C, respectively; these systematic errors are also evident by comparison with experimental data for natural peridotite systems. The older O’Neill and Wood (Contrib Mineral Petrol 70:59–70, 1979) version of the olivine–garnet Fe–Mg thermometer and all popular versions of the clinopyroxene–garnet Fe–Mg thermometer show unacceptably low precision, with discrepancies exceeding 200°C when compared to TA98 results for well-equilibrated xenoliths. Empirical correction to the Brey and Köhler (J Petrol 31:1353–1378, 1990) Ca-in-Opx thermometer and recalibration of the orthopyroxene–garnet thermometer, using well-equilibrated mantle xenoliths and TA98 temperatures as calibrants, are provided in this study to ensure consistency with TA98 estimates in the range 700–1,400°C. Observed discrepancies between the new orthopyroxene–garnet thermometer and TA98 for some localities can be interpreted in the light of orthopyroxene–garnet Fe³⁺ partitioning systematics and suggest localized and lateral variations in mantle redox conditions, in broad agreement with existing oxybarometric data. Kinetic decoupling of Ca–Mg and Fe–Mg exchange equilibria caused by transient heating appears to be common, but not ubiquitous, near the base of the lithosphere.     

拉萨地块林芝杂岩体含十字石石榴角闪岩的岩石学和变质过程研究

在拉萨地块林芝杂岩体中新发现的石榴角闪岩矿物组合为石榴子石、角闪石、十字石、绿泥石、斜长石、钠云母以及少量的钛铁矿和磷灰石。石榴角闪岩中石榴石核部富锰(Xsps=0.12~0.15)贫铁(Xalm=0.45~0.50)而石榴子石边部相对贫锰(Xsps=0.01~0.03)富铁(Xalm=0.60~0.65),表明石榴子石的核部和边部分别形成于变质作用两个不同阶段。从核部到边部,镁铝榴石升高而钙铝榴石降低,表现为进变质环带特征,这表明石榴子石核部形成于进变质过程。生长在不同的变质阶段的角闪石具有不同的成分特征,作为变质基性岩中罕见的富铝矿物,十字石的结构特征记录了不同变质阶段的信息,结合石榴石的成分和结构特征,为相平衡模拟研究其P-T演化过程提供了可能。我们利用Perplex相图模拟软件在Mn-NCKMASHO体系中模拟出该石榴角闪岩的视剖面图,利用石榴子石边部镁铝榴石和钙铝榴石含量等值线确定出石榴角闪岩峰期温压为:610~630oC,12×105~13×105k Pa,对应峰期矿物组合为石榴子石,角闪石,十字石和白云母。同时结合十字石保存的退变信息得到该石榴角闪岩经历了一个顺时针的变质演化轨迹。     

Formation of garnet polycrystals during metamorphic crystallization

Garnet polycrystals may form throughout the metamorphic history of a rock, starting at the earliest stages of garnet growth when closely spaced nuclei coalesce. In mica schist from Townshend Dam, VT, electron back-scattered diffraction (EBSD) analysis shows that garnet polycrystals possess two or more distinct lattice orientations separated by high-angle boundaries (28–61°). The minimum rotational displacements required to bring these lattice orientations into concordance with each other are commonly normal to the same low-energy planes that occur as crystal faces of euhedral garnet. There is no evidence for intracrystalline deformation, and the polycrystals therefore probably represent individual garnet crystals that coalesced during growth. The boundaries cross-cut growth zoning and inclusion trails of the polycrystals, indicating that early-formed polycrystals, once coalesced, behave chemically and physically as single crystals. Statistical analysis of a 3D, high-resolution X-ray computed tomographic data set of a large sample (912 cm³) of a Townshend Dam schist, combined with microprobe and EBSD analyses of garnet, are consistent with a high degree of clustering at all stages of garnet growth. The formation and prevalence of polycrystals implies that garnet nuclei impinged on each other and coalesced, and that coalescence was a common feature throughout garnet growth in the rock.     

Ultrahigh-pressure garnet peridotites from the devolatilization of sea-floor hydrated ultramafic rocks

Garnet peridotites occur in quartzofeldspathic gneisses in the Northern Qaidam Mountains, western China. They are rich in Mg and Cr, with mineral compositions similar to those in mantle peridotites found in other orogenic belts and as xenoliths in kimberlite. Garnet‐bearing lherzolites interlayered with dunite display oriented ilmenite and chromite lamellae in olivine and pyroxene lamellae in garnet that have been interpreted to indicate pressures in excess of 6 GPa. However, some garnet porphyroblasts include hornblende, chlorite and spinel + orthopyroxene symplectite after garnet; some clinopyroxene porphyroblasts include abundant actinolite/edenite, calcite and lizardite in the lherzolite; some olivine porphyroblasts (Fo₉₂) include an earlier generation Mg‐rich olivine (Fo_95–99), F‐rich clinohumite, pyroxene, chromite, anthophyllite/cummingtonite, Cl‐rich lizardite, carbonates and a new type of brittle mica, here termed ‘Ca‐phlogopite’, in the associated dunite. The pyrope content of garnet increases from core to rim, reaching the pyrope content (72 mol.%) of garnet typically found in the xenoliths in kimberlite. The simplest interpretation of these observations is that the rock association was formerly mantle peridotite emplaced into the oceanic crust that was subjected to serpentinization by seawater‐derived fluids near the sea floor. Dehydration during subduction to 3.0–3.5 GPa and 700 °C transformed these serpentinites into garnet lherzolite and dunite, depending on their Al and Ca contents. Pseudosection modelling using thermocalc shows that dehydration of the serpentinites is progressive, and involved three stages for Al‐rich and two stages for Al‐poor serpentinites, corresponding to the breakdown of the key hydrous minerals. Static burial and exhumation make olivine a pressure vessel for the pre‐subduction mineral inclusions during ultrahigh‐pressure (UHP) metamorphism. The time span of the UHP event is constrained by the clear interface between the two generations of olivine to be very short, implying rapid subduction and exhumation.     

蚌埠隆起区石榴辉石岩变质P-T轨迹的构建

蚌埠隆起区位于华北克拉通东南缘,胶—辽—吉造山带的最南端,主体由五河杂岩组成。前人对该地区的研究主要集中于同位素年代学和变质温压条件研究,其中变质P-T条件研究结果差异较大,以压力变化最为显著,对峰期变质P-T条件缺乏统一认识。本文对蚌埠隆起区石榴辉石岩进行了大量的岩相学、矿物化学成分分析,表明该岩石记录了3期变质作用,其中S-M1和S-M2的矿物组合类似为Grt+Cpx+Opx+Amp+Pl+Ilm,S-M3的矿物组合为Cpx+Amp+Pl+Grt （极边窄带）。结合变质温压条件分析和锆石U-Pb年代学分析,本次主要取得以下几点认识：1）石榴辉石岩WS047-1中记录的3期变质作用,温压条件分别为T-M1 = 616 ℃～647 ℃、P-M1 = 1.03～1.08 GPa,T-M2 = 721 ℃～837 ℃、P-M2 = 1.11～1.29 GPa和T-M3 = 531 ℃～607 ℃、P-M3 = 0.81～0.91 GPa,经历了由较高压力的角闪岩相→中-低麻粒岩相→角闪岩相的变质过程;2）据变质温压条件分析知,蚌埠隆起区具有顺时针的P-T轨迹特征,S-M1→S-M2和S-M2→S-M3分别为近等压升温和近等压降温的缓慢过程;3）石榴辉石岩锆石U-Pb年代学结果主要分为4组：1 839±13 Ma、1 925±31 Ma、2 041±55 Ma和2 762±14 Ma,其中峰值变质年代为1.93～1.84 Ga;4）结合温压条件和锆石U-Pb年代学分析结果,本文认为蚌埠隆起区的P-T轨迹与弗朗西斯科型俯冲或大陆碰撞环境的P-T轨迹较为类似,其应与1.93～1.84 Ga华北克拉通东、西陆块的碰撞拼合及胶—辽—吉造山带形成时限基本吻合。本次研究为深入理解华北克拉通的构造演化特征和蚌埠隆起区的变质作用及演化,提供了大量可靠的科学资料。     

Compositional zoning in garnet and kinetics of metamorphic crystallization

The kinetics of zoned garnet porphyroblast growth is exemplified in a sample of garnet-staurolite-biotite schist from the northern Ladoga region. The diffusion-controlled porphyroblast growth was accompanied by a decrease in the kinetic coefficient during phase reactions. Even at insignificant (1–2°C) thermal overstepping, the leading role of diffusion as a factor that controls kinetics of porphyroblast growth in medium-grade metapelites is consistent with the parameters of metamorphic crystallization: T = 500–650°C, t = 1 Ma; D _A1 ^app = 10^?14 cm²/s, L = 0.2–0.6 cm, r = 1–3 mm, ΔC _Al = 1.5 × 10^?4–1.5 × 10^?3 mol/cm³.     

On the mechanism of resorption zoning in metamorphic garnet

Abstract An analytical electron microscope study of almandine garnet from a metamorphosed Al–Fe‐rich rock revealed detailed composition profiles and defect microstructures of resorption zoning along fluid‐infiltrated veins and even into the garnet/ilmenite (inclusion) interface. This indicates a limited volume diffusion for the cations in substitution (mainly Ca and Fe) and an interface‐controlled partition for the extension of a composition‐invariant margin. A corrugated interface between the Ca‐rich margin/zone and the almandine garnet core is characterized by dislocation arrays and recovery texture further suggesting a resorption process facilitated by diffusion‐induced recrystallization, diffusion‐induced dislocation migration and diffusion–induced grain boundary migration. Integrated microstructural and chemical studies are essential for understanding the underlying mechanisms of processes such as garnet zoning and its modification. Without this understanding, it will not be possible to reliably use garnet compositions for thermobarometry and other applications that rely on garnet chemical information.     

A geothermobarometric investigation of garnet peridotites in the Western Gneiss Region of Norway

In the Western Gneiss Region of Norway are found numerous peridotite lenses which have been extensively recrystallized under amphibolite fades conditions during the Caledonian Orogeny. However, evidence for an earlier Caledonian high-pressure metamorphism has been recorded by abundant eclogite and granulite relicts within gneiss and by the presence of at least ten garnet perioditite bodies preserved within chlorite peridotites. Two garnet-bearing ultramafic assemblages have been recognized: olivine-orthopyroxene-clinopyroxene-garnet and olivine-ortho-pyroxene-pargasitic-amphibole-garnet.Except for olivine, minerals in the garnet peridotites are compositionally zoned, with relatively uniform cores and compositional gradients generally confined to the outer 200 micrometers, or less, of grains. The most common zoning patterns at grain margins are an increase in Fe/Mg in garnet, an increase in Al₂O₃ in orthopyroxene, and a decrease in Na₂O and Al₂O₃ in clinopyroxene, although there are exceptions to these patterns at two localities. These zoning patterns have developed mainly in response to cooling and decompression of the garnet peridotites.Application of geothermometers and barometers to the garnet peridotites has yielded temperatures of 770–860° C and pressures of 30–43 kb for cores of grains and consistently lower temperatures and pressures for rims, except for peridotites on Oterøy, where there is an apparent temperature increase from cores to rims.The petrologic and geothermobarometric evidence for most of the investigated garnet peridotites is compatible with their tectonic emplacement from the upper mantle into thickened continental crust during Caledonian collision of the Baltic and Greenland plates.     

Peak metamorphic temperatures from cation diffusion zoning in garnet

A model that relates the characteristic diffusion length and average cooling rate to peak temperature was developed for chemical diffusion in spherical geometries on the basis of geospeedometry principles and diffusion theory. The model is quantitatively evaluated for cation diffusion profiles in garnet. Important model parameters were calibrated empirically using diffusion zoning of Ca in garnet from the Pikwitonei Granulite Domain, a terrane for which the thermal history has been well characterized. The results are used: (i) to empirically test diffusion parameters for Mg and Fe(II) and (ii) to develop a tool that uses the diffusion zoning of these cations in garnet to constrain peak temperature conditions for garnet‐bearing rocks. The thermometric approach was externally tested by applying it to garnet crystals from various metamorphic terranes worldwide and comparing the results to published peak temperature estimates. The results overlap within uncertainties in all cases, but result that are based on Fe(II) and Mg chemical‐diffusion profiles are up to three times more precise than those acquired by conventional methods. The remarkable consistency of the results implies that the model is robust and provides a reliable means of estimating peak temperatures for different types of high‐grade metamorphic rock. The tool could be of particular advantage in rocks where critical assemblages for conventional thermometry do not occur or have been replaced during retrogression.     

The origin of garnet and clinopyroxene in “depleted” Kaapvaal peridotites

A detailed petrographic, major and trace element and isotope (Re–Os) study is presented on 18 xenoliths from Northern Lesotho kimberlites. The samples represent typical coarse, low-temperature garnet and spinel peridotites and span a P–T range from 60 to 150 km depth. With the exception of one sample (that belongs to the ilmenite–rutile–phlogopite–sulphide suite (IRPS) suite first described by [B. Harte, P.A. Winterburn, J.J. Gurney, Metasomatic and enrichment phenomena in garnet peridotite facies mantle xenoliths from the Matsoku kimberlite pipe, Lesotho. In: Menzies, M. (Ed.), Mantle metsasomatism. Academic Press, London 1987, 145–220.]), all samples considered here have high Mg# and show strong depletion in CaO and Al₂O₃. They have bulk rock Re depletion ages (T_RD) >2.5 Ga and are therefore interpreted as residua from large volume melting in the Archaean. A characteristic of Kaapvaal xenoliths, however, is their high SiO₂ concentrations, and hence, modal orthopyroxene contents that are inconsistent with a simple residual origin of these samples. Moreover, trace element signatures show strong overall incompatible element enrichment and REE disequilibrium between garnet and clinopyroxene. Textural and subtle major element disequilibria were also observed. We therefore conclude that garnet and clinopyroxene are not co-genetic and suggest that (most) clinopyroxene in the Archaean Kaapvaal peridotite xenoliths is of metasomatic origin and crystallized relatively recently, possibly from a melt precursory to the kimberlite.

Possible explanations for the origin of garnet are exsolution from a high-temperature, Al- and Ca-rich orthopyroxene (indicating primary melt extraction at shallow levels) or a majorite phase (primary melting at >6 GPa). Mass balance calculations, however, show that not all garnet observed in the samples today is of a simple exsolution origin. The extreme LREE enrichment (sigmoidal REE pattern in all garnet cores) is also inconsistent with exsolution from a residual orthopyroxene. Therefore, extensive metasomatism and probably re-crystallization of the lithosphere after melt-depletion and garnet exsolution is required to obtain the present textural and compositional features of the xenoliths. The metasomatic agent that modified or perhaps even precipitated garnet was a highly fractionated melt or fluid that might have been derived from the asthenosphere or from recycled oceanic crust. Since, to date, partitioning of trace elements between orthopyroxene and garnet/clinopyroxene is poorly constrained, it was impossible to assess if orthopyroxene is in chemical equilibrium with garnet or clinopyroxene. Therefore, further trace element and isotopic studies are required to constrain the timing of garnet introduction/modification and its possible link with the SiO₂ enrichment of the Kaapvaal lithosphere.     

The Luliangshan garnet peridotite massif of the North Qaidam UHPM belt, NW China - a review of its origin and metamorphic evolution

The Luliangshan garnet peridotite massif is an ultramafic complex in the North Qaidam UHPM belt, NW China. The strongly layered complex comprising garnet-bearing dunite, garnet-harzburgite, garnet-lherzolite and garnet-pyroxenite and garnet-free dunite, occurs together with eclogite embedded in various continental gneisses. The geological setting, the internal structure, bulk-composition, rare earth elements, isotopic and mineral composition data show that the garnet peridotite derives from a middle Ordovician Alaskan-type layered sub-arc cumulate intrusion of ascending mantle wedge melts. An abyssal peridotite protolith can be excluded. During the Ordovician-Silurian continental collision, thickening and foundering, the Luliangshan peridotite complex was exposed to ultrahigh pressures (UHP) reaching 5.5 GPa possibly >6 GPa at temperatures of 900 °C (perhaps up to 1000 °C) corresponding to a depth of ∼200 km. The extreme pressure conditions have been derived from thermobarometry using mineral compositions of the garnet peridotite assemblages, but they are supported by a wealth of decompression-induced mineral exsolutions in UHP minerals and by diamond inclusion in zircon. The Luliangshan garnet peridotite has experienced four stages of retrograde overprint during exhumation that lasted into the Devonian: (i) decompression-induced unmixing of the UHP minerals; (ii) garnet kelyphitisation; (iii) amphibole overprinting and (iv) serpentinization. Hydrous minerals occurring within peak metamorphic assemblage represent pseudo-inclusions, that is reaction products of reactions related to various stages of decompression and cooling rather than prograde inclusions during porphyroblast growth.     

Ostwald ripening of garnet in high P/T metamorphic rocks

This paper presents a theoretical formulation of Ostwald ripening of garnet and discusses the importance of the process during high pressure and low temperature (high P/T) metamorphism. The growth rate of garnet due to Ostwald ripening is formulated for the system consisting of minerals and an intergranular medium. Crystal size distribution (CSD) of garnets are examined and compared with the theoretical distribution for Ostwald ripening. Two types of CSDs are recognized. One is consistent with the theoretical prediction of size distribution while the other is wider than the theoretical distribution. The former CSD applies to samples in which garnets show homogeneous spatial distributions. The latter CSD applies to samples in which garnets show heterogeneous spatial distributions such as in clusters or layers. These relations suggest that the heterogeneity of spatial distributions results in a heterogeneity of concentration of garnet, causing the wide distributions. The mean diameter (dg) has a large variation in samples having narrow distributions. Ostwald ripening explains well the similar patterns of CSD in these samples with different dg because of a scaling law. Compositional profiles of garnets with different size are consistent with Ostwald ripening rather than nucleation and growth kinetics. This suggests that the CSDs result from Ostwald ripening. Magnitude of heating rate will determine which mechanism controls CSD. Nucleation and growth kinetics are dominant when heating rate is large. On the other hand, Ostwald ripening is dominant when heating rate is small. CSDs of garnets in high P/T metamorphic rocks are consistent with the latter case.