Mineral chemistry of ultramafic and mafic cumulates as an indicator of the arc-related origin of the Mersin ophiolite (southern Turkey)

The Mersin ophiolite, represented by approximately 6-km-thick oceanic lithospheric section on the southern flank of the Taurus calcareous axis, formed in the Mesozoic Neo-Tethyan ocean some time during Late Cretaceous in southern Turkey. The ultramafic and mafic cumulates having over 3 km thickness consist of dunite ± chromite, wehrlite, clinopyroxenite at the bottom and pass into gabbroic cumulates in which leucogabbro, olivine-gabbro and anorthosite are seen. Crystallization order is olivine (Fo₉₁₋₈₀) ± chromian spinel (Cr# 60-80), clinopyroxene (Mg#₉₅₋₇₇), plagioclase (An_95.6−91.6) and orthopyroxene (Mg#₆₈₋₇₇). Mineral chemistry of ultramafic and mafic cumulates suggest that highly magnesian olivines, clinopyroxenes and absence of plagioclase in the basal ultramafic cumulates are in good agreement with products of high-pressure crystal fractionation of primary basaltic melts beneath an island-arc environment. Major, trace element geochemistry of the cumulative rocks also indicate that Mersin ophiolite was formed in an arc environment. Coexisting Ca-rich plagioclase and Forich olivine in the gabbroic cumulates show arc cumulate gabbro characteristics. Field relations as well as the geochemical data support that Mersin ophiolite formed in a supra-subduction zone tectonic setting in the southern branch of the Neo-Tethys in southern Turkey.     

Petrological characteristics of podiform chromitites and associated peridotites of the Pan African Proterozoic ophiolite complexes of Egypt

Mafic-ultramafic fragments of a dismembered ophiolite complex are abundant in the late Precambrian Pan African belt of the Eastern Desert of Egypt and north-east Sudan. The ultramafic bodies in the Eastern Desert of Egypt are mostly characterised by the harzburgite–dunite–chromitite association. Because of their severe metamorphism, almost all primary silicates were converted to secondary minerals and we use the chrome spinel as a reliable petrogenetic indicator. The podiform chromitite deposits are common as small and irregularly shaped masses in the central and southern parts of the Eastern Desert. They strongly vary in texture, degree of alteration and chemical composition of chrome spinel. The podiform chromitites exhibit a wide range of composition from high Cr to high Al varieties. The Cr of chrome spinel ranges from 0.65 to 0.85 in dunite, quite similar in the high-Cr chromitite, whereas it is around 0.5 in harzburgite. Primary hydrous mineral inclusions, amphibole and phlogopite, in chrome spinel are reported for the first time from the Pan African Proterozoic podiform chromitites. The petrological characteristics of Pan African podiform chromitites and associated peridotites of Egypt are similar to those of Phanerozoic ophiolites. The Proterozoic podiform chromitites may have formed in the same way as the Phanerozoic ones, namely by melt-harzburgite reaction and subsequent melt mixing. The similarity of the mantle section of the late Proterozoic and the Phanerozoic ophiolites suggests that the thermal conditions controlling genesis of the crust–mantle system basically have not changed since the late Proterozoic era. The Pan African harzburgite is very similar to abyssal peridotite at fast-spreading ridges, and the high-Cr, low-Ti character of spinel in chromitite and dunite indicates a genetic link with a supra-subduction zone setting. The late Proterozoic ophiolites of Egypt are possibly a fragment of oceanic lithosphere modified by arc-related magmatic rocks, or a fragment of back-arc basin lithosphere. Received: 26 October 1999 / Accepted: 28 June 2000     

Genesis of garnet peridotites in the Sulu UHP belt: Examples from the Chinese continental scientific drilling project-main hole, PP1 and PP3 drillholes

The main hole (MH), and pre-pilot holes PP1, and PP3 of the Chinese Continental Scientific Drilling Project (CCSD) penetrated three different garnet peridotite bodies in the Sulu ultrahigh pressure (UHP) metamorphic belt, which are 80 m, 120 m, and 430 m thick, respectively. The bodies occur as tectonic blocks hosted in eclogite (MH peridotite) and gneisses (PP1 and PP3 peridotites). The peridotites in the MH are garnet wehrlites, whose protoliths were ultramafic cumulates based on olivine compositions (Fo_79-89) and other geochemical features. Zoned garnet and omphacite (with 4-5 wt.% Na₂O) are typical metamorphic minerals in these rocks, and, along with P-T estimates based on mineral pairs, suggest that the rocks have undergone UHP metamorphism. SHRIMP U-Pb isotope dating of zircon from the garnet wehrlite yielded a Paleozoic protolith age (ca. 346-461 Ma), and a Mesozoic UHP metamorphic age (ca. 220-240 Ma). The peridotites in PP1 consist of interlayered garnet (Grt)-bearing and garnet-free (GF) peridotite. Both types of peridotite have depleted mantle compositions (Mg# = 90-92) and they display transitional geochemical features. The intercalated layers probably reflect variations in partial melting rather than pressure variations during metamorphism, and the garnets may have been formed by exsolution from orthopyroxene during exhumation. These peridotites were probably part of the mantle wedge above the subduction zone that produced the UHP metamorphism and thus belonged to the North China Block before its tectonic emplacement. The exhumation of the subducted Yangtze Block brought these mantle fragments to shallow crustal levels. The ultramafic rocks in PP3 are dominantly dunite with minor garnet dunite. Their high Mg# (92-93) and relatively uniform chemical compositions indicate that they are part of a depleted mantle sequence. The presence of garnet replacing spinel and enclosing pre-metamorphic minerals such as olivine, clinopyroxene and spinel suggests that these rocks have undergone progressive metamorphism. SHRIMP U-Pb isotope dating of zircon from these rocks yielded two age groups: 726 ± 56 Ma for relic magmatic zircon grains and 240 ± 2.7 Ma for the newly formed metamorphic zircon. The older group is similar in age to granitic intrusions within the Dabie-Sulu belt, suggesting that the PP3 garnet peridotite may record the early emplacement of the peridotite into the crust. The younger dates coincide with the age of UHP metamorphism during continent-continent collision between the Yangtze and North China Blocks, suggesting that these peridotites were subducted to depths equivalent to the coesite facies and later exhumed. Thus, the garnet peridotites in the CCSD cores include both ultramafic rocks that existed originally in the subducted plate and rocks from the mantle wedge above the subducted plate, i.e., part of the North China Block.     

Ultramafic Xenoliths from the Bearpaw Mountains, Montana, USA: Evidence for Multiple Metasomatic Events in the Lithospheric Mantle beneath the Wyoming Craton

Ultramafic xenoliths in Eocene minettes of the Bearpaw Mountainsvolcanic field (Montana, USA), derived from the lower lithosphereof the Wyoming craton, can be divided based on textural criteriainto tectonite and cumulate groups. The tectonites consist ofstrongly depleted spinel lherzolites, harzburgites and dunites.Although their mineralogical compositions are generally similarto those of spinel peridotites in off-craton settings, somecontain pyroxenes and spinels that have unusually low Al₂O₃contents more akin to those found in cratonic spinel peridotites.Furthermore, the tectonite peridotites have whole-rock majorelement compositions that tend to be significantly more depletedthan non-cratonic mantle spinel peridotites (high MgO, low CaO,Al₂O₃ and TiO₂) and resemble those of cratonic mantle. Thesecompositions could have been generated by up to 30% partialmelting of an undepleted mantle source. Petrographic evidencesuggests that the mantle beneath the Wyoming craton was re-enrichedin three ways: (1) by silicate melts that formed mica websteriteand clinopyroxenite veins; (2) by growth of phlogopite fromK-rich hydrous fluids; (3) by interaction with aqueous fluidsto form orthopyroxene porphyroblasts and orthopyroxenite veins.In contrast to their depleted major element compositions, thetectonite peridotites are mostly light rare earth element (LREE)-enrichedand show enrichment in fluid-mobile elements such as Cs, Rb,U and Pb on mantle-normalized diagrams. Lack of enrichment inhigh field strength elements (HFSE; e.g. Nb, Ta, Zr and Hf)suggests that the tectonite peridotites have been metasomatizedby a subduction-related fluid. Clinopyroxenes from the tectoniteperidotites have distinct U-shaped REE patterns with strongLREE enrichment. They have ¹⁴³Nd/¹⁴⁴Nd values that range from0·5121 (close to the host minette values) to 0·5107,similar to those of xenoliths from the nearby Highwood Mountains.Foliated mica websterites also have low ¹⁴³Nd/¹⁴⁴Nd values (0·5113)and extremely high ⁸⁷Sr/⁸⁶Sr ratios in their constituent phlogopite,indicating an ancient (probably mid-Proterozoic) enrichment.This enriched mantle lithosphere later contributed to the formationof the high-K Eocene host magmas. The cumulate group rangesfrom clinopyroxene-rich mica peridotites (including abundantmica wehrlites) to mica clinopyroxenites. Most contain >30%phlogopite. Their mineral compositions are similar to thoseof phenocrysts in the host minettes. Their whole-rock compositionsare generally poorer in MgO but richer in incompatible traceelements than those of the tectonite peridotites. Whole-rocktrace element patterns are enriched in large ion lithophileelements (LILE; Rb, Cs, U and Pb) and depleted in HFSE (Nb,Ta Zr and Hf) as in the host minettes, and their Sr–Ndisotopic compositions are also identical to those of the minettes.Their clinopyroxenes are LREE-enriched and formed in equilibriumwith a LREE-enriched melt closely resembling the minettes. Thecumulates therefore represent a much younger magmatic event,related to crystallization at mantle depths of minette magmasin Eocene times, that caused further metasomatic enrichmentof the lithosphere. KEY WORDS: ultramafic xenoliths; Montana; Wyoming craton; metasomatism; cumulates; minette     

Subcalcic clinopyroxenites and associated ultramafic xenoliths in alkali basalt near Glen Innes, northeastern New South Wales, Australia

An alkali basalt near Glen Innes, northeastern New South Wales, contains a suite of Cr-diopside group ultramafic xenoliths which includes some spinel peridotites but which is dominated by a diverse spinel pyroxenite assemblage. Pyroxenite xenoliths range from subcalcic clinopyroxenites (composed largely of unmixed prismatic subcalcic clinopyroxene megacrystals and lesser orthopyroxene megacrystals) to equant mosaic textured websterites (orthopyroxene and Ca-rich clinopyroxene ± spinel). Rare orthopyroxenite xenoliths also occur. The pyroxenite xenoliths are characterised by high 100Mg/(Mg + Fe²⁺) ratios (M˜ 90) and low concentrations of Ti, K, P, La, Ce and Zr. The websterites are mineralogically and chemically similar to many spinel pyroxenites occurring as layers or dykes in peridotite massifs such as those at Ronda in southern Spain and at Ariège (French Pyrénées). T / P estimates indicate crystallization temperatures of 1250–1350 °C for subcalcic clinopyroxene-orthopyroxene megacrystal pairs and 900–1000 °C for the equilibrated mosaic textured websterites and associated peridotites at pressures of 9–13 kbar. Subcalcic clinopyroxene megacrystals, websterites and orthopyroxenites have LREE-depleted chondrite-normalised REE abundances with (La/Yb)_CN < 1 and their convex-upwards REE patterns are typical of subcalcic clinopyroxene-dominated cumulates. The pyroxenites are not residua from partially melted pyroxenite layers or dykes in mantle peridotites nor are they completely crystallized protobasaltic or protopicritic magmas. They are interpreted as high-pressure crystal segregations from basaltic magmas (probably mildly alkaline or transitional) flowing within narrow mantle conduits (the flow crystallization model of Irving, 1980). The parental magma(s) was Ti-poor (0.6–0.7% TiO₂) and relatively Mg-rich (M˜ 74 − 70). Pyroxenite genesis was a two-stage process involving crystallization of tschermakitic subcalcic clinopyroxenes and orthopyroxenes  ±spinel as liquidus or near-liquidus phases at 1250–1350 °C and 9–13 kbar to yield “primary” subcalcic clinopyroxenites which then re-equilibrated at 900–1000 °C and similar pressures to produce the mosaic textured “secondary” websterites. The pyroxenites show a wide range of ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr values (0.513298–0.512473 and 0.702689–0.704659, respectively). Their isotopic ratios appear to have been variably modified by exchange with adjacent mantle peridotites or migrating basaltic melts. Received: 11 December 1995 / Accepted: 3 December 1996     

Early Cambrian oceanic plagiogranite in the Silvretta Nappe,eastern Alps: geochemical,zircon U-Pb and Rb-Sr data from garnet-hornblende-plagioclase gneisses

 Garnet–hornblende–plagioclase gneisses rich in incompatible elements occur in the crystalline basement of the Austro-Alpine Silvretta nappe and are associated with clinopyroxene norites and harzburgite cumulates. It is proposed here that the gneisses were formerly oceanic plagiogranites. An ε_{Nd( 530 )} value of +5.6 for the gneisses as well as initial ⁸⁷Sr/⁸⁶Sr values of 0.7036–0.7037 for the gabbroic rocks and 0.7026–0.7027 for the ultramafic rocks suggest a mantle source for this rock association. The geochemical characteristics of the garnet–hornblende–plagioclase gneisses indicate that their precursors were derived by fractional crystallization from a basaltic parent magma, by the same process which produced the adjacent clinopyroxene norites and ultramafic cumulates as well. The combined U–Pb upper intercept ages of zircons from two gneiss samples yield an igneous crystallization age of 532±30 Ma, similar to previously dated (mostly calc-alkaline) orthogneisses in the same area. High-quality transparent zircons showed the least degree of discordance, but contain extremely low U and Pb levels. The rock suite, including this plagiogranite, was emplaced within oceanic crust which formed in the latest Precambrian–early Palaeozoic off the northern continental margin of Gondwana. Received: 26 April 1996 / Accepted: 2 August 1996     

Melt extraction and melt refertilization in mantle peridotite of the Coast Range ophiolite: an LA–ICP–MS study

The middle Jurassic Coast Range Ophiolite (CRO) is one of the most important tectonic elements in western California, cropping out as tectonically dismembered elements that extend 700 km from south to north. The volcanic and plutonic sections are commonly interpreted to represent a supra-subduction zone (SSZ) ophiolite, but models specifying a mid-ocean ridge origin have also been proposed. These contrasting interpretations have distinctly different implications for the tectonic evolution of the western Cordillera in the Jurassic. If an SSZ origin is confirmed, we can use the underlying mantle peridotites to elucidate melt processes in the mantle wedge above the subduction zone. This study uses laser ablation–inductively coupled plasma–mass spectrometry (LA–ICP–MS) to study pyroxenes in peridotites from four mantle sections in the CRO. Trace element signatures of these pyroxenes record magmatic processes characteristic of both mid-ocean ridge and supra-subduction zone settings. Group A clinopyroxene display enriched REE concentrations [e.g., Gd (0.938–1.663 ppm), Dy (1.79–3.24 ppm), Yb (1.216–2.047 ppm), and Lu (0.168–0.290 ppm)], compared to Group B and C clinopyroxenes [e.g., Gd (0.048–0.055 ppm), Dy (0.114–0.225 ppm), Yb (0.128–0.340 ppm), and Lu (0.022–0.05 ppm)]. These patterns are also evident in orthopyroxene. The differences between these geochemical signatures could be a result of a heterogeneous upper mantle or different degrees of partial melting of the upper mantle. It will be shown that CRO peridotites were generated through fractional melting. The shapes of REE patterns are consistent with variable degrees of melting initiated within the garnet stability field. Models call for 3% dry partial melting of MORB-source asthenosphere in the garnet lherzolite field for abyssal peridotites and 15–20% further partial melting in the spinel lherzolite field, possibly by hydrous melting for SSZ peridotites. These geochemical variations and occurrence of both styles of melting regimes within close spatial and temporal association suggest that certain segments of the CRO may represent oceanic lithosphere, attached to a large-offset transform fault and that east-dipping, proto-Franciscan subduction may have been initiated along this transform.     

The composition of melt and fluid inclusions in spinel of peridotite xenoliths from Avacha volcano (Kamchatka)

This work considers the studies of melt and fluid inclusions in spinel of ultramafic rocks in the mantle wedge beneath Avacha volcano (Kamchatka). The generations of spinel were identified: 1 is spinel (Sp-I) of the “primary” peridotites, has the highest magnesium number (#0.69–0.71), highest contents of Al₂O₃ and lowest contents of Cr₂O₃ (26.2–27.1 and 37.5–38.5 wt %, respectively), and the absence in it of any fluid and melt inclusions; 2 is spinel (Sp-II) of the recrystallized peridotites, has lower magnesium number (Mg# 0.64–0.61) and the content of Al₂O₃ (18–19 wt %), a higher content of Cr₂O₃ (45.4–47.2 wt %) and the presence of primary fluid inclusions; 3 is spinel (Sp-III) that is characterized by the highest content of Cr₂O₃ (50.2–55.4 wt %), the lowest content of Al₂O₃ (13.6–16.6 wt %), and the presence of various types of primary melt inclusions. The data obtained indicate that metasomatic processing of “primary” peridotites occurred under the influence of high concentrated fluids of mainly carbonate-water-chloride composition with influx of the following petrogenic elements: Si, Al, Fe, Ca, Na, K, S, F, etc. This process was often accompanied by a local melting of the metasomatized substrate at a temperature above 1050°C with the formation of melts close to andesitic.     

Petrogenesis of ultramafic and mafic xenoliths from Mesozoic basanites in southern Sweden: constraints from mineral chemistry

Jurassic basanite necks occurring at the junction of two major fault zones in Scania contain ultramafic (peridotites, pyroxenites) and mafic xenoliths, which together indicate a diversity of upper mantle and lower crustal assemblages beneath this region. The peridotites can be subdivided into lherzolites, dunites and harzburgites. Most lherzolites are porphyroclastic, containing orthopyroxene and olivine porphyroclasts. They consist of Mg-rich silicates (Mg# = Mg/(Mg + Fe_tot) × 100; 88–94) and vermicular spinel. Calculated equilibration temperatures are lower in porphyroclastic lherzolites (975–1,007°C) than in equigranular lherzolite (1,079°C), indicating an origin from different parts of the upper mantle. According to the spinel composition the lherzolites represent residues of 8–13% fractional melting. They are similar in texture, mineralogy and major element composition to mantle xenoliths from Cenozoic Central European volcanic fields. Dunitic and harzburgitic peridotites are equigranular and only slightly deformed. Silicate minerals have lower to similar Mg# (83–92) as lherzolites and lack primary spinel. Resorbed patches in dunite and harzburgite xenoliths might be the remnants of metasomatic processes that changed the upper mantle composition. Pyroxenites are coarse, undeformed and have silicate minerals with partly lower Mg# than peridotites (70–91). Pyroxenitic oxides are pleonaste spinels. According to two-pyroxene thermometry pyroxenites show a large range of equilibration temperatures (919–1,280°C). In contrast, mafic xenoliths, which are mostly layered gabbronorites with pyroxene- and plagioclase-rich layers, have a narrow range of equilibration temperatures (828–890°C). These temperature ranges, together with geochemical evidence, indicate that pyroxenites and gabbroic xenoliths represent mafic intrusions within the Fennoscandian crust.     

Multi-stage melt–rock interaction in the Mt. Maggiore (Corsica, France) ophiolitic peridotites: microstructural and geochemical evidence

Spinel and plagioclase peridotites from the Mt.Maggiore (Corsica, France) ophiolitic massif record a composite asthenosphere–lithosphere history of partial melting and subsequent multi-stage melt–rock interaction. Cpx-poor spinel lherzolites are consistent with mantle residues after low-degree fractional melting (F = 5–10%). Opx + spinel symplectites at the rims of orthopyroxene porphyroclasts indicate post-melting lithospheric cooling (T = 970–1,100°C); this was followed by formation of olivine embayments within pyroxene porphyroclasts by melt–rock interaction. Enrichment in modal olivine (up to 85 wt%) at constant bulk Mg values, and variable absolute REE contents (at constant LREE/HREE) indicate olivine precipitation and pyroxene dissolution during reactive porous melt flow. This stage occurred at spinel-facies depths, after incorporation of the peridotites in the thermal lithosphere. Plagioclase-enriched peridotites show melt impregnation microtextures, like opx + plag intergrowths replacing exsolved cpx porphyroclasts and interstitial gabbronoritic veinlets. This second melt–rock interaction stage caused systematic chemical changes in clinopyroxene (e.g. Ti, REE, Zr, Y increase), related to the concomitant effects of local melt–rock interaction at decreasing melt mass, and crystallization of small (<3%) trapped melt fractions. LREE depletion in minerals of the gabbronoritic veinlets indicates that the impregnating melts were more depleted than normal MORB. Preserved microtextural evidence of previous melt–rock interaction in the impregnated peridotites suggests that they were progressively uplifted in response to lithosphere extension and thinning. Migrating melts were likely produced by mantle upwelling and melting related to extension; they were modified from olivine-saturated to opx-saturated compositions, and caused different styles of melt–rock interaction (reactive spinel harzburgites, vs. impregnated plagioclase peridotites) depending on the lithospheric depths at which interaction occurred. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Petrology of ultramafic nodules from São Tomé Island, Cameroon Volcanic Line (oceanic sector)

Ultramafic xenoliths were found in recent alkali basalts from São Tomé Island. These include spinel peridotites (lherzolites, harzburgites and dunites) and pyroxenites (orthopyroxenites and clinopyroxenites). Textures and mineral compositions indicate that pyroxenites originated from crystal/liquid separation processes operating on magmas similar to those giving rise to their present host rocks whereas spinel peridotite xenoliths had an accidental origin; Fo (>89) and Ni (>0.36 wt.%) contents in olivines, Mg# (91–95) of orthopyroxenes and low Ti in clinopyroxene (primary crystals: TiO₂<0.06 wt.%) and in spinel (TiO₂<0.1 wt.%) are within the range reported for abyssal peridotites, indicating São Tomé spinel peridotites represent refractory residues of melting. Nevertheless, the lack of correlation between mineral chemistry and modal composition suggests that spinel peridotite xenoliths are not simple residues and were affected by infiltration of fluid/melts within the mantle. The wide temperature range obtained for spinel peridotites (700 to >1150 °C) is compatible with a long period of pre-entrainment cooling supporting Fitton's [Tectonophysics 94 (1983) 473] hypothesis that proposes oceanic lithosphere uprising in the Cameroon Volcanic Line prior to the initiation of the current thermal regime, related to São Tomé magmatism. The association of upper mantle (peridotite) xenoliths with igneous cumulates (pyroxenites) suggests that the spinel peridotite suite originated in the uppermost mantle above the São Tomé magma storage zone(s), probably in a region of high strain rate, near the boundary between the mantle and the overlying oceanic crust.     

Compositional variations and heterogeneity in fertile lithospheric mantle: peridotite xenoliths in basalts from Tariat,Mongolia

Clinopyroxene-rich, poorly metasomatised spinel lherzolites are rare worldwide but predominate among xenoliths in five Quaternary basaltic eruption centres in Tariat, central Mongolia. High-precision analyses of the most fertile Tariat lherzolites are used to evaluate estimates of primitive mantle compositions; they indicate Mg#_PM = 0.890 while lower Mg# in the mantle are likely related to metasomatic enrichments in iron. Within a 10 × 20 km area, and between ~45 and ≥60 km depth, the sampled xenoliths suggest that the Tariat mantle does not show km-scale chemical heterogeneities and mainly consists of residues after low-degree melt extraction at 1–3 GPa. However, accessory (<1%) amphibole and phlogopite are unevenly distributed beneath the eruption centres. Ca abundances in olivine are controlled by temperature whereas Al and Cr abundances also depend on Cr/Al in coexisting spinel. Comparisons of conventional and high-precision analyses obtained for 30 xenoliths show that high-quality data, in particular for whole-rocks and olivines, are essential to constrain the origin of mantle peridotites. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Geochemical syntheses among the cratonic,off-cratonic and orogenic garnet peridotites and their tectonic implications

Garnet-bearing mantle peridotites, occurring as either xenoliths in volcanic rocks or lenses/massifs in high-pressure and ultrahigh-pressure terrenes within orogens, preserve a record of deep lithospheric mantle processes. The garnet peridotite xenoliths record chemical equilibrium conditions of garnet-bearing mineral assemblage at temperatures (T) ranging from ~700 to 1,400°C and pressures (P) > 1.6–8.9 GPa, corresponding to depths of ~52–270 km. A characteristic mineral paragenesis includes Cr-bearing pyropic garnet (64–86 mol% pyrope; 0–10 wt% Cr₂O₃), Cr-rich diopside (0.5–3.5 wt% Cr₂O₃), Al-poor orthopyroxene (0–5 wt% Al₂O₃), high-Cr spinel (Cr/(Cr + Al) × 100 atomic ratio = 2–86) and olivine (88–94 mol% forsterite). In some cases, partial melting, re-equilibration involving garnet-breakdown, deformation, and mantle metasomatism by kimberlitic and/or carbonatitic melt percolations are documented. Isotope model ages of Archean and Proterozoic are ubiquitous, but Phanerozoic model ages are less common. In contrast, the orogenic peridotites were subjected to ultrahigh-pressure (UHP) metamorphism at temperature ranging from ~700 to 950°C and pressure >3.5–5.0 GPa, corresponding to depths of >110–150 km. The petrologic comparisons between 231 garnet peridotite xenoliths and 198 orogenic garnet peridotites revealed that (1) bulk-rock REE (rare earth element) concentrations in xenoliths are relatively high, (2) clinopyroxene and garnet in orogenic garnet peridotites show a highly fractionated REE pattern and Ce-negative anomaly, respectively, (3) Fo contents of olivines for off-cratonic xenolith are in turn lower than those of orogenic garnet and cratonic xenolith but mg-number of garnet for orogenic is less than that of off-cratonic and on-cratonic xenolith, (4) Al₂O₃, Cr₂O₃, CaO and Cr# of pyroxenes and chemical compositions of whole rocks are very different between these garnet peridotites, (5) orogenic garnet peridotites are characterized by low T and high P, off-cratonic by high T and low P, and cratonic by medium T and high P and (6) garnet peridotite xenoliths are of Archean or Proterozoic origin, whereas most of orogenic garnet peridotites are of Phanerozoic origin. Taking account of tectonic settings, a new orogenic garnet peridotite exhumation model, crust-mantle material mixing process, is proposed. The composition of lithospheric mantle is additionally constrained by comparisons and compiling of the off-cratonic, on-cratonic and orogenic garnet peridotite.     

Petrological constraints on the cooling history of high-temperature garnet peridotite massifs in lower Austria

High-temperature peridotite massifs occur as lensoid bodies with high-pressure granulites in the southern Bohemian massif. In lower Austria the peridotites comprise garnet lherzolites lacking primary spinel, rare garnet and garnet-spinel harzburgites, and harzburgites containing Cr-rich primary spinel instead of garnet. These phase assemblages suggest initial high-pressure equilibration and are consistent with results from garnet-orthopyroxene geobarometry indicating equilibration at around 3–3.5 GPa. Maximum temperature estimates obtained on core compositions of coexisting minerals from the peridotites are not higher than ca. 1100 °C. In contrast, pyroxene megacryst compositions, garnet exsolution textures in the garnet pyroxenites, and results from geothermometry indicate much higher original equilibration temperatures in most of the pyroxenites (up to 1400 °C). High temperatures, modal zoning, the occasional presence of Mg-rich garnetites and chemical evidence suggest that the pyroxenites are cumulates which crystallized from low-degree melts derived from the sub-lithospheric mantle. Isothermal interpolation of the high temperatures to an upper mantle adiabat suggests that the melts were derived from a minimum depth of 180–200 km. The formation of small garnet II grains and garnet exsolution lamellae in the pyroxenites and pyroxene megacrysts may reflect isobaric cooling of the cumulates from temperatures above 1400 °C to ca. 1100–1200 °C (at 3–3.5 GPa) to approach the ambient lithospheric isotherm. This model differs from other models in which the formation of garnet II was explained by an increase in pressure during cooling in a subduction zone. Isobaric cooling was followed by near-isothermal decompression from 3–3.5 GPa to 1.5–2 GPa at 1000–1200 °C, as indicated by the increase of Al in pyroxenes near garnet. Further cooling in the spinel lherzolite stability field is indicated by spinel exsolution lamellae in pyroxenes from lherzolites. The formation of symplectites and kelyphites indicate sub-millimetre scale re-equilibration during exhumation in the course of the Carboniferous collision in the Bohemian massif. The peridotite massifs represent fragments of normal (non-cratonic) lithospheric mantle from a Paleozoic convergent plate margin. Received: 22 July 1996 / Accepted 28 February 1997     

Contrasting P-T conditions recorded in ultramafic high-pressure rocks from the Variscan Schwarzwald (F.R.G.)

 This paper presents mineralogical and textural data as well as thermobarometric calculations on ultramafic high-pressure rocks from the Variscan basement of the Schwarzwald (F.R.G.). The rocks form small isolated bodies within low-pressure / high-temperature gneisses and migmatites. The results of this study constrain contrasting P-T evolutions for four garnet-bearing ultramafic high-pressure rocks. Two magnesian garnet-spinal peridotites sampled near the southern margin of the Central Schwarzwald Gneiss Complex (CSGC) were equilibrated at 670–740^° C and 1.4–1.8 GPa. These P-T conditions are similar to those recorded by eclogites intercalated in the same basement unit. Two garnet websterites sampled from the northern part of the CSGC have comparatively low Mg/(Mg+Fe) and low Cr and Ni abundances and are interpreted as former cumulates. These rocks most probably experienced an initial high-temperature stage within the spinel peridotite stability field, followed by re-equilibration at 740–850^° C / 3.2–4.3 GPa and subsequent recrystallization at lower pressures. Further petrologic studies have to reveal whether ultramafic high-pressure rocks of the Schwarzwald can generally be assigned to these two groups which are mainly defined by contrasting peak pressures. Received: 22 August 1994 / Accepted: 19 January 1995     

Melt- versus fluid-induced metasomatism in spinel to garnet wedge peridotites (Ulten Zone, Eastern Italian Alps): clues from trace element and Li abundances

The peridotite bodies of the Ulten Zone (Upper Austroalpine, Italian Eastern Alps) are enclosed in Variscan migmatites and derive from a mantle wedge environment. They display the progressive transformation of porphyroclastic spinel peridotites (T=1,200°C; P=1.5 GPa) into fine-grained garnet–amphibole peridotites (T=850°C; P=3 GPa). Detailed bulk-rock and mineral trace element analyses of a sample suite documenting the entire metamorphic evolution of the peridotites revealed several stages of metasomatism. The spinel peridotites derive from a depleted mantle that became enriched in some large ion lithophile element (LILE) and light rare earth elements (LREE). The same signature pertains to clinopyroxene and orthopyroxene, indicating that this metasomatic signature was acquired at the recorded temperature of 1,200°C. Such a temperature is considerably above the wet peridotite solidus and hence the metasomatic agent must have been a hydrous melt. Moreover, the Li-enrichment of the spinel-facies pyroxenes (up to 24 ppm Li) reflects disequilibrium distribution after exchange with a presumably mafic melt. ^cpx/opx D _Li=3–7 and ^cpx/ol D _Li=2.7–8 indicate that the spinel-facies clinopyroxene hosts higher Li amounts than the coexisting minerals. LREE fractionation, variable LREE enrichment, LILE enrichment with respect to HFSE (average clinopyroxene Pb _N /Nb _N =16–90) in spinel lherzolites can be related to chromatographic effects of porous melt flow. The significant enrichment of pyroxenes from the spinel lherzolites in Pb, U and Li indicates that the metasomatic melt was subduction-related. All these features suggest that the spinel lherzolites formed a mantle wedge layer percolated by melts carrying recycled crustal components and rising from a deeper source of subduction magmas. The garnet + amphibole peridotites equilibrated at temperatures well below the wet solidus in the presence of an aqueous fluid. Bulk-rock trace element patterns display pronounced positive anomalies in Cs, Ba, Pb and U and moderate enrichment in Li, indicating addition of a crustal component to the mantle rocks. Amphibole hosts most of these trace elements. Clinopyroxene displays high LILE/HFSE (Pb _N /Nb _N =300–600), low Ce/Pb (1.4–2.7 in garnet-facies clinopyroxene compared with 2.6–24.5 in the spinel-facies one) and variable LILE and LREE enrichments. The coupled increase of modal amphibole, Sr and Pb, together with positive Pb–Sr and Pb–U correlations, further indicate that incompatible element influx in these samples was fluid-mediated. In the garnet-facies samples, amphibole and, interestingly, olivine have similarly high Li concentrations as clinopyroxene, leading to ^cpx/amph D _Li=0.7 and ^cpx/ol D _Li=0.7–0.8, the latter being up to ten times lower than in the spinel-facies rocks. Due to its high modal abundance, olivine is the main host of Li in the garnet–amphibole peridotites. The observed metasomatic features provide evidence for the infiltration of an aqueous fluid in the mantle wedge above a subducting slab. This fluid most likely derived from subducted crustal rocks that underwent partial melting. Successive retrograde re-equilibration during exhumation of the garnet peridotite is accompanied by garnet and clinopyroxene breakdown and amphibole formation. This process produced minor changes, such as an increase of HREE and Li in amphibole, and an increase of Li in olivine. The general trace element signature remains essentially unchanged during retrogression and further hydration, indicating that fluids with a similar composition to the one present at the garnet–amphibole peridotite formation, were responsible for increased amphibole formation. The combined evidence from the metamorphic and metasomatic evolution indicates that the peridotites experienced first corner flow in a mantle wedge, followed by subduction and finally entrapment and exhumation within a crustal slab. During their entire history the Ulten peridotites were percolated first by melts and then by aqueous fluids, which added recycled crustal components to the mantle wedge.     

Textures and geochemistry of the Saramta peridotites (Siberian craton): Melting and refertilization during early evolution of the continental lithospheric mantle

The Saramta peridotite massif is located within the Sharyzhalgai complex, SW margin of the Siberian craton. The Saramta massif was formed in the Archean and then juxtaposed with granulites of crystalline basement of the Siberian craton. The Saramta harzburgites are highly refractory in terms of lack of residual clinopyroxene, olivine Mg-number (up to 0.937), and spinel Cr-number (∼0.5), suggesting high degree of partial melting. Detailed study of their microstructures shows that they have extensively reacted with a SiO₂-rich melt, leading to the crystallization of orthopyroxene, clinopyroxene, amphibole and spinel at the expense of olivine. The major element compositions of the least reacted harzburgites are similar to the residues of refractory peridotites produced by the fractional melting (initial melting pressures >3 GPa and melt fractions ∼40%). Moreover, non-residual clinopyroxenes are highly depleted in Yb, Zr and Ti, but highly enriched in LREE. A two-stage history is proposed for the Saramta peridotite: (1) primitive mantle underwent depletion in the garnet stability field followed by melting in the spinel stability field; (2) refractory harzburgites underwent refertilization by SiO₂-rich melt in supra-subduction zone. Rare Saramta lherzolites probably formed from more refractory harzburgites as a result of such a melt–rock reaction. The Saramta peridotites are similar to low-T coarse-grained peridotites of subcratonic mantle. Processes of their formation, as reflected by textures and composition of minerals of the Saramta peridotites, are characteristic of the early stages of subcratonic mantle formation.     

Geodynamic implications of ophiolitic chromitites in the La Cabaña ultramafic bodies,Central Chile

Chromitites (>80% volume chromite) hosted in two ultramafic bodies (Lavanderos and Centinela Bajo) from the Palaeozoic metamorphic basement of the Chilean Coastal Cordillera were studied in terms of their chromite composition, platinum-group element (PGE) abundances, and Re-Os isotopic systematics. Primary chromite (Cr# = 0.64–0.66; Mg# = 48.71–51.81) is only preserved in some massive chromitites from the Centinela Bajo ultramafic body. This chemical fingerprint is similar to other high-Cr chromitites from ophiolite complexes, suggesting that they crystallized from arc-type melt similar to high-Mg island-arc tholeiites (IAT) and boninites in supra-subduction mantle. The chromitites display enrichment in IPGE (Os, Ir, Ru) over PPGE (Rh, Pt, Pd), with PGE concentrations between 180 and 347 ppb, as is typical of chromitites hosted in the mantle of supra-subduction zone (SSZ) ophiolites. Laurite (RuS₂)-erlichmanite (OsS₂) phases are the most abundant inclusions of platinum-group minerals (PGM) in chromite, indicating crystallization from S-undersaturated melts in the sub-arc mantle. The metamorphism associated with the emplacement of the ultramafic bodies in the La Cabaña has been determined to be ca. 300 Ma, based on K-Ar dating of fuchsite. Initial ¹⁸⁷Os/¹⁸⁸Os ratios for four chromitite samples, calculated for this age, range from 0.1248 to 0.1271. These isotopic compositions are well within the range of chromitites hosted in the mantle section of other Phanaerozoic ophiolites. Collectively, these mineralogical and geochemical features are interpreted in terms of chromite crystallization in dunite channels beneath a spreading centre that opened a marginal basin above a supra-subduction zone. This implies that chromitite-bearing serpentinites in the metamorphic basement of the Coastal Cordillera are of oceanic-mantle origin and not oceanic crust as previously suggested. We suggest that old subcontinental mantle underlying the hypothetical Chilenia micro-continent was unroofed and later altered during the opening of the marginal basin. This defined the compositional and structural framework in which the protoliths of the meta-igneous and meta-sedimentary rocks of the Eastern and Western Series of the Chilean Coastal Cordillera basement were formed.     

Supra-subduction zone magmatism of the Neyriz ophiolite,Iran: constraints from geochemistry and Sr-Nd-Pb isotopes

The Neyriz ophiolite along the northeast flank of the Zagros fold-thrust belt in southern Iran is an excellent example of a Late Cretaceous supra-subduction zone (SSZ)-related ophiolite on the north side of the Neotethys. The ophiolite comprises a mantle sequence including lherzolite, harzburgite, diabasic dikes, and cumulate to mylonitic gabbro lenses, and a crustal sequence comprising a sheeted dike complex and pillow lavas associated with pelagic limestone and radiolarite. Mantle harzburgites contain less CaO and Al₂O₃, are depleted in rare earth elements, and contain spinels that are more Cr-rich than lherzolites. Mineral compositions of peridotites are similar to those of both abyssal and SSZ- peridotites. Neyriz gabbroic rocks show boninitic (SSZ-related) affinities, while crustal rocks are similar to early arc tholeiites. Mineral compositions of gabbroic rocks resemble those of SSZ-related cumulates such as high forsterite olivine, anorthite-rich plagioclase, and high-Mg# clinopyroxene. Initial εNd(t) values range from +7.9 to +9.3 for the Neyriz magmatic rocks. Samples with radiogenic Nd overlap with least radiogenic mid-ocean ridge basalts and with Semail and other Late Cretaceous Tethyan ophiolitic rocks. Initial ⁸⁷Sr/⁸⁶Sr ranges from 0.7033 to 0.7044, suggesting modification due to seafloor alteration. Most Neyriz magmatic rocks are characterized by less radiogenic ²⁰⁷Pb/²⁰⁴Pb (near the northern hemisphere reference line), suggesting less involvement of sediments in their mantle source. Our results for Neyriz ophiolite and the similarity to other Iranian Zagros ophiolites support a subduction initiation setting for its generation.     

Petrological investigation of the Ganyu peridotite in the Sulu ultrahigh-pressure terrane, eastern China

The ultramafic body sampled in the Chinese Continental Scientific Drilling (CCSD) Hole PP3 is located in the eastern part of the Dabie-Sulu UHP metamorphic belt near Donghai County. It is about 480 m thick, and consists chiefly of garnet peridotite, dunite and serpentinite. The principal minerals include olivine, chromium spinel, diopside, enstatite, garnet with minor secondary augite, phlogopite and amphibole. Both the olivine and orthopyroxene are highly magnesian, and the garnet is pyropic with 5.4-6.4% CaO and 0.3-3.3% Cr₂O₃. Two generations of clinopyroxene are present; an early diopside followed by augite. Chromium spinels are highly variable with Cr#s (100Cr / (Cr + Al)) between 51 and 89, and their compositions reflect different processes of formation, namely partial melting and eclogite, amphibole and greenschist facies metamorphism. The Mg#s (100 Mg / (Mg + Fe²⁺))of the spinels correlate positively with the Cr#s but negatively with oxygen fugacity. Based on the spinel compositions the ultramafic rocks originated in the shallow mantle, then subducted to depths of more than 100 km and finally exhumed to the surface. They underwent partial melting at shallow depths, mostly in the spinel facies, and were later transformed into garnet peridotites during deep subduction. All of the rocks were weakly metasomatized during exhumation and were subjected to retrograde metamorphism.