Melt–peridotite interaction in the shallow lithospheric mantle of the North China Craton: evidence from melt inclusions in the quartz-bearing orthopyroxene-rich websterite from Hannuoba

To better understand the origin, migration, and evolution of melts in the lithospheric mantle and their roles on the destruction of the North China Craton (NCC), we conducted a petrological and geochemical study on a quartz-bearing orthopyroxene-rich websterite xenolith from Hannuoba, the NCC, and its hosted melt and fluid inclusions. Both clinopyroxene and orthopyroxene in the xenolith contain lots of primary and secondary inclusions. High-temperature microthermometry of melt inclusions combined with Raman spectroscopy analyses of coexisting fluid inclusions shows that the entrapment temperature of the densest inclusions was ~1215°C and the pressure ~11.47 kbar, corresponding to a depth of ~38 km, i.e. within the stability of the spinel lherzolite. Intermediate pressure inclusions probably reflect progressive fluid entrapment over a range of depths during ascent, whereas the low-pressure inclusions (P < 2 kbar) may represent decrepitated primary inclusions. In situ laser-ablation ICP-MS analyses of major and trace elements on individual melt inclusions show that the compositions of these silicate melt inclusions in clinopyroxene and orthopyroxene are rich in SiO₂, Al₂O₃, and alkalis but poor in TiO₂ and strongly enriched in light rare earth elements (LREEs) and large ion lithophile elements (LILEs), with negative anomalies of high-field strength elements (HFSEs). These characteristics suggest that the silica-rich melts could be derived from the partial melting of subducted oceanic slab. Therefore, this kind of quartz-bearing orthopyroxene-rich websterite may be produced by interaction between the slab-derived melts with the mantle peridotite. This study provides direct evidence for the origin, migration, and evolution of melts in the lithospheric mantle, which may play an important role in the destruction of the NCC.     

Heterogeneous lithospheric mantle metasomatism in the eastern North China Craton: He–Ar isotopes in peridotite xenoliths from Cenozoic basalts

The abundances and isotopic compositions of Helium and Argon have been analyzed in a suite of fresh spinel peridotite xenoliths in Cenozoic basalts from the eastern North China Craton (NCC) by step-wise heating experiments, to investigate the nature of noble gas reservoirs in the subcontinental lithospheric mantle beneath this region. The xenoliths include one harzburgite collected from Hebi in the interior of the NCC, two lherzolites from Hannuoba at the northern margin of the craton, and three lherzolites from Shanwang and Nushan on the eastern margin. ³He/⁴He ratios in most of the xenoliths are similar to those of mid-ocean ridge basalts (MORB) or slightly lower (2–10.5 Ra, where Ra is the ³He/⁴He ratio of the atmosphere), suggesting mixing of MORB-like and radiogenic components. One olivine separate from Nushan has a helium value of 25.3 Ra, probably suggesting cosmogenic ³He addition. The ⁴⁰Ar/³⁶Ar ratios vary from atmospheric value (296) to 1625, significantly lower than the MORB value. Available data of the peridotite xenoliths indicate the He and Ar isotopic systematics of the mantle reservoirs beneath the NCC can be interpreted as mixtures of at least three end-members including MORB-like, radiogenic and atmospheric components. We suggest that the MORB-like noble gases were derived from the underlying asthenosphere during mantle upwelling, whereas the radiogenic and recycled components probably were incorporated into the lithospheric mantle during circum-craton subduction of oceanic crust. Available data suggest that the MORB-like fluids are better preserved in the interior of the NCC, whereas the radiogenic ones are more prevalent at the margins. The Paleo-Asian ocean subduction system probably was responsible for the enriched and recycled noble gas signatures on the northern margin of the craton, while the Pacific subduction system could account for the observed He–Ar isotopic signatures beneath the eastern part. Therefore, integration of helium and argon isotopes reflects heterogeneous metasomatism in the lithospheric mantle and demonstrates the critical importance of lithospheric mantle modification related to both circum-craton subduction of oceanic crust and asthenospheric upwelling beneath the eastern NCC.     

Mafic xenoliths in Proterozoic kimberlites from Eastern Dharwar Craton,India: Mineralogy and P–T regime

Mafic xenoliths of garnet pyroxenite and eclogite from the Wajrakarur, Narayanpet and Raichur kimberlite fields in the Archaean Eastern Dharwar Craton (EDC) of southern India have been studied. The composition of clinopyroxene shows transition from omphacite (3–6 wt% Na₂O) in eclogites to Ca pyroxene (<3 wt% Na₂O) in garnet pyroxenites. Some of the xenoliths have additional phases such as kyanite, enstatite, chromian spinel or rutile as discrete grains. Clinopyroxene in a rutile eclogite has an X_Mg value of 0.70, which is unusually low compared to the X_Mg range of 0.91–0.97 for all other samples. Garnet in the rutile eclogite is also highly iron-rich with an end member composition of Prp_26.5Alm_52.5Grs_14.7Adr_5.1TiAdr_0.3Sps_1.0Uv_0.1. Garnets in several xenoliths are Cr-rich with up to 8 mol% knorringite component. Geothermobarometric calculations in Cr-rich xenoliths yield different P–T ranges for eclogites and garnet pyroxenites with average P–T conditions of 36 kbar and 1080 °C, and 27 kbar and 830 °C, respectively. The calculated P–T ranges approximate to a 45 mW m^?2 model geotherm, which is on the higher side of the typical range of xenolith/xenocryst geotherms (35–45 mW m^?2) for several Archaean cratons in the world. This indicates that the EDC was hotter than many other shield regions of the world in the mid-Proterozoic period when kimberlites intruded the craton. Textural and mineral chemical characteristics of the mafic xenoliths favour a magmatic cumulate process for their origin as opposed to subducted and metamorphosed oceanic crust.     

Evolution of subcontinental lithospheric mantle beneath eastern China: Re–Os isotopic evidence from mantle xenoliths in Paleozoic kimberlites and Mesozoic basalts

The ages of subcontinental lithospheric mantle beneath the North China and South China cratons are less well-constrained than the overlying crust. We report Re–Os isotope systematics of mantle xenoliths entrained in Paleozoic kimberlites and Mesozoic basalts from eastern China. Peridotite xenoliths from the Fuxian and Mengyin Paleozoic diamondiferous kimberlites in the North China Craton give Archean Re depletion ages of 2.6–3.2 Ga and melt depletion ages of 2.9–3.4 Ga. No obvious differences in Re and Os abundances, Os isotopic ratios and model ages are observed between spinel-facies and garnet-facies peridotites from both kimberlite localities. The Re–Os isotopic data, together with the PGE concentrations, demonstrate that beneath the Archean continental crust of the eastern North China Craton, Archean lithospheric mantle of spinel- to diamond-facies existed without apparent compositional stratification during the Paleozoic. The Mesozoic and Cenozoic basalt-borne peridotite and pyroxenite xenoliths, on the other hand, show geochemical features indicating metasomatic enrichment, along with a large range of the Re–Os isotopic model ages from Proterozoic to Phanerozoic. These features indicate that lithospheric transformation or refertilization through melt-peridotite interaction could be the primary mechanism for compositional changes during the Phanerozoic, rather than delamination or thermal-mechanical erosion, despite the potential of these latter processes to play an important role for the loss of garnet-facies mantle. A fresh garnet lherzolite xenolith from the Yangtze Block has a Re depletion age of ∼1.04 Ga, much younger than overlying Archean crustal rocks but the same Re depletion ages as spinel lherzolite xenoliths from adjacent Mesozoic basalts, indicating Neoproterozoic resetting of the Re–Os system in the South China Craton.     

Carbonate-rich melt infiltration in peridotite xenoliths from the Eurasian–North American modern plate boundary (Chersky Range,Yakutia)

A suite of mainly spinel peridotite and subordinate pyroxenite xenoliths and megacrysts were studied in detail, enabling us to characterize upper mantle conditions and processes beneath the modern North American–Eurasian continental plate boundary. The samples were collected from 37-Ma-old basanites cropping out in the Main Collision Belt of the Chersky Range, Yakutia Republic (Russian Far East). The spinel lherzolites reflect a mantle sequence, equilibrated at temperatures of 890–1,025 °C at pressures of 1.1–2 GPa, with melt extraction estimated to be around 2–6 %. The spinel harzburgites are characterized by lower P–T equilibration conditions and estimated melt extraction up to 12 %. Minor cryptic metasomatic processes are recorded in the clinopyroxene trace elements, revealing that percolating hydrous fluid-rich melts and basaltic melts affected the peridotites. One of the lherzolites preserves a unique melt droplet with primary dolomite in perfect phase contact with Na-rich aluminosilicate glass and sodalite. On the basis of the well-constrained P–T frame of the xenolith suite, as well as the rigorously documented melt extraction and metasomatic history of this upper mantle section, we discuss how a carbonated silicate melt infiltrated the lherzolite at depth and differentiated into an immiscible carbonate and silicate liquid shortly before the xenolith was transported to the surface by the host basalt. Decreasing temperatures triggered crystallization of primary dolomite from the carbonate melt fraction and sodalite as well as quenched glass from the Na-rich aluminosilicate melt fraction. Rapid entrainment and transport to the Earth’s surface prevented decarbonatization processes as well as reaction phenomena with the host lherzolite, preserving this exceptional snapshot of upper mantle carbonatization and liquid immiscibility.     

Geochemistry of spinel-hosted amphibole inclusions in abyssal peridotite: insight into secondary melt formation in melt–peridotite reaction

Spinel-hosted hydrous silicate mineral inclusions are often observed in dunite and troctolite as well as chromitite. Their origin has been expected as products associated with melt–peridotite reaction, based on the host rock origin. However, the systematics in mineralogical and geochemical features are not yet investigated totally. In this study, we report geochemical variations of the spinel-hosted pargasite inclusions in reacted harzburgite and olivine-rich troctolite collected from Atlantis Massif, an oceanic core complex, in the Mid-Atlantic Ridge. The studied samples are a good example to examine geochemical variations in the inclusions because the origin and geological background of the host rocks have been well constrained, such as the reaction between MORB melt and depleted residual harzburgite beneath the mid-ocean ridge spreading center. The trace-element compositions of the pargasite inclusions are characterized by not only high abundance of incompatible elements but also the LREE and HFSE enrichments. Distinctive trace-element partitioning between the pargasite inclusion and the host-rock clinopyroxene supports that the secondary melt instantaneously formed by the reaction is trapped in spinel and produces inclusion minerals. While the pargasite geochemical features can be interpreted by modal change reaction of residual harzburgite, such as combination of orthopyroxene decomposition and olivine precipitation, degree of the LREE enrichment as well as variation of HREE abundance is controlled by melt/rock ratio in the reaction. The spinel-hosted hydrous inclusion could be embedded evidence indicating melt–peridotite reaction even if reaction signatures in the host rock were hidden by other consequent reactions.     

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.     

Multistage melt/fluid-peridotite interactions in the refertilized lithospheric mantle beneath the North China Craton: constraints from the Li–Sr–Nd isotopic disequilibrium between minerals of peridotite xenoliths

Elemental and Li–Sr–Nd isotopic data of minerals in spinel peridotites hosted by Cenozoic basalts allow us to refine the existing models for Li isotopic fractionation in mantle peridotites and constrain the melt/fluid-peridotite interaction in the lithospheric mantle beneath the North China Craton. Highly elevated Li concentrations in cpx (up to 24 ppm) relative to coexisting opx and olivine (<4 ppm) indicate that the peridotites experienced metasomatism by mafic silicate melts and/or fluids. The mineral δ⁷Li vary greatly, with olivine (+0.7 to +5.4‰) being isotopically heavier than coexisting opx (−4.4 to −25.9‰) and cpx (−3.3 to −21.4‰) in most samples. The δ⁷Li in pyroxenes are considerably lower than the normal mantle values and show negative correlation with their Li abundances, likely due to recent Li ingress attended by diffusive fractionation of Li isotopes. Two exceptional samples have olivine δ⁷Li of −3.0 and −7.9‰, indicating the existence of low δ⁷Li domains in the mantle, which could be transient and generated by meter-scale diffusion of Li during melt/fluid-peridotite interaction. The ¹⁴³Nd/¹⁴⁴Nd (0.5123–0.5139) and ⁸⁷Sr/⁸⁶Sr (0.7018–0.7062) in the pyroxenes also show a large variation, in which the cpx are apparently lower in ⁸⁷Sr/⁸⁶Sr and slightly higher in ¹⁴³Nd/¹⁴⁴Nd than coexisting opx, implying an intermineral Sr–Nd isotopic disequilibrium. This is observed more apparently in peridotites having low ⁸⁷Sr/⁸⁶Sr and high ¹⁴³Nd/¹⁴⁴Nd ratios than in those with high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd, suggesting that a relatively recent interaction existed between an ancient metasomatized lithospheric mantle and asthenospheric melt, which transformed the refractory peridotites with highly radiogenic Sr and unradiogenic Nd isotopic compositions to the fertile lherzolites with unradiogenic Sr and radiogenic Nd isotopic compositions. Therefore, we argue that the lithospheric mantle represented by the peridotites has been heterogeneously refertilized by multistage melt/fluid-peridotite interactions.     

Small volume andesite magmas and melt–mush interactions at Ruapehu, New Zealand: evidence from melt inclusions

Historical eruptions from Mt. Ruapehu (New Zealand) have been small (<0.001 km³ of juvenile magma) and have often occurred without significant warning. Developing better modelling tools requires an improved understanding of the magma storage and transport system beneath the volcano. Towards that end, we have analysed the volatile content and major element chemistry of groundmass glass and phenocryst-hosted melt inclusions in erupted samples from 1945 to 1996. We find that during this time period, magma has been stored at depths of ~2–9 km, consistent with inferences from geophysical data. Our data also show that Ruapehu magmas are relatively H₂O-poor (<2 wt%) and CO₂-rich (≤1,000 ppm) compared to typical arc andesites. Surprisingly, we find that melt inclusions are often more evolved than their transporting melt (as inferred from groundmass glass compositions). Furthermore, even eruptions that are separated by less than 2 years exhibit distinct major element chemistry, which suggests that each eruption involved magma with a unique ascent history. From these data, we infer that individual melt batches rise through, and interact with, crystal mush zones formed by antecedent magmas. From this perspective, we envision the magmatic system at Ruapehu as frequently recharged by small magma inputs that, in turn, cool and crystallise to varying degrees. Melts that are able to erupt through this network of crystal mush entrain (to a greater or lesser extent) exotic crystals. In the extreme case (such as the 1996 eruption), the resulting scoria contain melt inclusion-bearing crystals that are exotic to the transporting magma. Finally, we suggest that complex interactions between recharge and antecedent magmas are probably common, but that the small volumes and short time scales of recharge at Ruapehu provide a unique window into these processes.     

Mathiasite-loveringite and priderite in mantle xenoliths from the Alto Paranaíba Igneous Province,Brazil: genesis and constraints on mantle metasomatism

Alkali-bearing Ti oxides were identified in mantle xenoliths enclosed in kimberlite-like rocks from Limeira 1 alkaline intrusion from the Alto Paranaíba Igneous Province, southeastern Brazil. The metasomatic mineral assemblages include mathiasite-loveringite and priderite associated with clinopyroxene, phlogopite, ilmenite and rutile. Mathiasite-loveringite (55–60 wt.% TiO₂; 5.2–6.7 wt.% ZrO₂) occurs in peridotite xenoliths rimming chromite (～50 wt.% Cr₂O₃) and subordinate ilmenite (12–13.4 wt.% MgO) in double reaction rim coronas. Priderite (Ba/(K+Ba)< 0.05) occurs in phlogopite-rich xenoliths as lamellae within Mg-ilmenite (8.4–9.8 wt.% MgO) or as intergrowths in rutile crystals that may be included in sagenitic phlogopite. Mathiasite-loveringite was formed by reaction of peridotite primary minerals with alkaline melts. The priderite was formed by reaction of peridotite minerals with ultrapotassic melts. Disequilibrium textures and chemical zoning of associated minerals suggest that the metasomatic reactions responsible for the formation of the alkali-bearing Ti oxides took place shortly prior the entrainment of the xenoliths in the host magma, and is not connected to old (Proterozoic) mantle enrichment events.     

Melt percolation and reaction atop a plume: evidence from the poikiloblastic peridotite xenoliths from Borée (Massif Central, France)

Poikiloblastic harzburgite xenoliths (P-type) from Borée, France are characterised by large (>1 cm), essentially unstrained olivines and high equilibrium temperatures (>1200 °C). Mineralogical data, trace element abundances and Sr-Nd-O isotopes of the constituent minerals are consistent with formation as a result of melt percolation-reactions in a lherzolite precursor during lithospheric erosion by an upwelling plume. This petrogenetic model contrasts with previous models involving isochemical recrystallisation from a granular lherzolite precursor (G-type) or derivation as metacumulates from tholeiitic magmas. Numerical simulation of percolation reactions at the lithosphere-plume boundary using the plate model of Vernières et al. (1997) indicates that the different textured xenoliths may represent mantle from different levels in a percolation-reaction column. If correct then the P-type harzburgites resulted from pyroxene-dissolving and olivine-producing reactions at increasing melt fraction (>3%) at the lower part of column (base of the lithosphere), whereas the G-type lherzolites were located within the low-porosity domain (<0.1%) above a permeability barrier, and are formed through a melt-rock reaction at decreasing melt mass. Given the very low melt fraction, the REE fractionation in this zone is controlled by chromatographic effects coupled with source effects of reaction. The variations in porosity, melt/rock ratio and melt-rock reaction mechanism are believed to be responsible for the diversity of REE patterns and striking correlation between REE abundance and texture in Borée xenoliths. Received: 15 June 1997 / Accepted: 7 January 1998     

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.     

Petrogenesis of adamellites from eastern Shandong Province: geochronological,geochemical, and Sr–Nd–Pb isotopic evidence

Geochronology, geochemistry, and whole-rock Sr–Nd–Pb isotopes were studied on a suite of Mesozoic adamellites from eastern China to characterize their ages and petrogenesis. Sensitive high-resolution ion microprobe U–Pb zircon analyses were done, yielding consistent ages of 123.2 ± 1.8 to 122.1 ± 2.1 Ma for the samples. These rocks belong to the alkaline magma series in terms of K₂O + Na₂O contents (8.45–9.58 wt.%) and to the shoshonitic series based on their high K₂O contents (5.23–5.79 wt.%). The adamellites are further characterized by high light rare earth element contents [(La/Yb)_N = 14.96–45.99]; negative Eu anomalies (δEu = 0.46–0.75); positive anomalies in Rb, Th, Pb, and U; and negative anomalies in Sr, Ba, and high field-strength elements (i.e. Nb, Ta, P, and Ti). In addition, all of the adamellites in this study display relatively low radiogenic Sr [(⁸⁷Sr/⁸⁶Sr)_i = 0.7081–0.7089] and negative ?_Nd(t) values from –16.70 to –17.80. These results suggest that the adamellites were derived from low-degree partial melting of an enriched lithospheric mantle below the North China Craton (NCC). The parent magmas likely experienced fractional crystallization of potassium feldspar, plagioclase and Fe–Ti oxides (e.g. rutile, ilmenite, and titanite), apatite, and zircon during the ascent of alkaline rocks without crustal contamination.     

A micro-scale investigation of melt production and extraction in the upper mantle based on silicate melt pockets in ultramafic xenoliths from the Bakony–Balaton Highland Volcanic Field (Western Hungary)

Mantle xenoliths in Neogene alkali basalts of the Bakony–Balaton Highland Volcanic Field (Western Hungary) frequently have melt pockets that contain silicate minerals, glass, and often carbonate globules. Textural, geochemical and thermobarometric data indicate that the melt pockets formed at relatively high pressure through breakdown of mainly amphibole as a result of temperature increases accompanied, in most cases, by the influx of external metasomatic agents. New elemental and Sr–Nd–Pb isotope data show that in several xenoliths the external agent was either a LIL-enriched aqueous fluid or a CO₂-rich fluid, whereas in other xenoliths the melt pockets were additionally enriched in LREE and sometimes HFSE, suggesting metasomatism by a silicate melt. The compositional character of the external agents might have been inherited by melting of a hydrated and probably carbonated deeper lithospheric component, which itself was metasomatized by melts with significant slab-derived components. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Paleocene adakite Au–Fe bearing rocks,Mezcala, Mexico: evidence from geochemical characteristics

The Au–Fe mineralized granitoids at Mezcala district have a porphyry texture with a quartz+feldspar microcrystalline matrix and phenocrysts of plagioclase, quartz (with reaction rims), hornblende and biotite. The primary minerals are oligoclase–andesine, microcline and β-quartz. The accessory minerals are biotite, hornblende and, in minor amounts, apatite+zircon+sphene+titanomagnetite. Some intrusive rocks present abundant hornblende autoliths. Based on the petrography and bulk geochemistry of these granitoids, they are classified as monzonite, tonalite (the most abundant) and granodiorite with a strong calc-alkaline trend in potassium (K₂O=3.8% average). The bulk and trace elements chemistry is SiO₂=63.8%, Al₂O₃=15.83%, Fe₂O₃+MgO+MnO+TiO=6.52%; V=76.7 ppm, Cr=50.2 ppm, Ni=19.7 ppm, Sr=694 ppm. These granitoids show a strong depletion in heavy rare-earth elements (HREE), with average values of Yb=1 ppm and Y=13 ppm, this being the characteristic geochemical signature for adakite. The trace elements content suggests that the adakite granitoids from Mezcala were formed within a tectonic framework of volcanic arc related to the interaction between the Farallon and North America plates. This interaction occurred during the Paleocene after the Laramide Orogeny (post-collision zone) in a fast convergent thick continental crust (>50 km) subduction regime. The original magma is interpreted as being the product of partial melting of an amphibolite–eclogite transition zone source with little contribution of the mantle wedge. Along with the hydration processes, a metallic fertility also took place in the area. The geochemical signature of the adakites within the granitoids rocks represents a characteristic guide for further exploration for Au-rich skarn-type ore deposits in southern México.     

Underplating and assimilation–fractional crystallization of Mesozoic intrusions in the Tongling area,Anhui Province,East China: evidence from xenoliths and host plutons

This paper presents new petrographic observations and geochemical and microprobe analyses for the Laomiaojishan, Xiaotongguanshan, and Tianebaodanshan intrusions in the Tongguanshan mineral district, East China. The plutons vary in composition from quartz monzonitic diorite to pyroxene monzonitic diorite, and contain gabbroic to dioritic xenoliths. The Xiaotongguanshan intrusion yields a SHRIMP zircon U–Pb age of 139.5±2.9 Ma, indicating Late Jurassic to Early Cretaceous magmatism in the Lower Yangtze River Valley. Relative to host rocks, the gabbro and diorite xenoliths are low in SiO₂ (52.03–54.61 wt‐%), Al₂O₃ (12.87–14.43 wt‐%), and total alkalis (Na₂O+K₂O; 5.26–6.30 wt‐%), but high in MgO (5.41–11.66 wt‐%); the host rocks have high SiO₂ (59.97–64.44 wt‐%), Al₂O₃ (16.43–17.59 wt‐%), and total alkalis (6.67–8.25 wt‐%), but are low in MgO (1.52–2.50 wt‐%). Concentrations of rare earth elements (REEs) in the xenoliths (165.70–190.40 ppm) are similar to those in the host rocks (166.12–185.95 ppm), although the ratio of light REEs to heavy REEs in the xenoliths (3.39–4.27) is lower than that in the host plutons (4.86–5.94). All of the analysed rocks show similar REE patterns, although the xenoliths display marked positive Eu anomalies and the host rocks show slightly negative Eu anomalies. Values of epsilon Nd (t) ranges from ?4.9 to ?9.9 in the gabbro xenoliths and from ?11.4 to ?11.9 in the host intrusives. Initial ⁸⁷Sr/⁸⁶Sr ratios are 0.7064–0.7073 in the xenoliths and 0.7072–0.7084 in the quartz monzonitic diorite host rocks. Crystallization temperatures of hornblende and plagioclase in the gabbro xenoliths, diorite xenoliths, and host rocks are 816, 773–790, and 664–725°C, respectively, based on an amphibole–plagioclase geothermometer. The pressures recorded by these phases indicate that they formed at depths of 26, 12–15, and 3–4 km, respectively, based on an aluminum‐in‐hornblende geobarometer. The petrological and geochemical features of the analysed intrusions and xenoliths are consistent with their derivation from basic to intermediate‐acidic magmas that possibly formed via a series of complex interactions between underplated, mantle‐derived basaltic magma and varying amounts of middle‐ to lower‐crustal material, followed by assimilation–fractional crystallization.     

Experimental peridotite–melt reaction at one atmosphere: a textural and chemical study

Sieve-textured clinopyroxene and spinel are common in mantle xenoliths and have been interpreted to be the result of partial melting, mantle metasomatism and host magma–xenolith reaction during transport. In this paper, we test the latter hypothesis with a series of reduced and oxidized experiments at 1,200 and 1,156°C at one atmosphere using a synthetic leucitite melt and discs of natural peridotite. Our results show that sieve texture development on clinopyroxene and spinel in mantle xenoliths is the result of a multistage reaction process. In the first step, orthopyroxene undergoes incongruent dissolution to produce a silica and alkali-rich melt together with olivine. As this melt migrates along grain boundaries it causes incongruent dissolution of clinopyroxene and spinel. The incongruent dissolution mechanism involves complete dissolution of the clinopyroxene or spinel followed by nucleation and growth of a secondary clinopyroxene or spinel once the reacting melt is saturated. The reaction of orthopyroxene, clinopyroxene and spinel with infiltrated host magma results in a range of melt compositions that are very similar to those interpreted to be due to very small degrees of partial melting. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.