Cumulating processes at the crust-mantle transition zone inferred from Permian mafic-ultramafic xenoliths (Puy Beaunit,France)

Ultramafic and mafic xenoliths of magmatic origin, sampled in the Beaunit vent (northern French Massif Central), derive from the Permian (257 Ma) Beaunit layered complex (BLC) that was emplaced at the crust-mantle transition zone (∼1 GPa). These plutonic xenoliths are linked to a single fractional crystallisation process in four steps: peridotitic cumulates; websteritic cumulates; Al-rich mafic cumulates (plagioclase, pyroxenes, garnet, amphibole and spinel) and finally low-Al mafic cumulates. This sequence of cumulates can be related to the compositional evolution of hydrous Mg basaltic magma that evolved to high-Al basalt and finally to andesitic basalt. Sr and Nd isotopic compositions confirm the co-genetic character of the various magmatic xenoliths and argue for an enriched upper mantle source comparable to present mantle wedges above subduction zones. LILE, LREE and Pb enrichment are a common feature of all xenoliths and argue for an enriched sub-alkaline transitional parental magma. The existence of a Permian magma chamber at 30 km depth suggests that the low-velocity zone observed locally beneath the Moho probably does not represent an anomalous mantle but rather a sequence of mafic/ultramafic cumulates with densities close to those of mantle rocks.     

Liquid line of descent of a basanitic liquid at 1.5 Gpa: constraints on the formation of metasomatic veins

The metasomatism observed in the oceanic and continental lithosphere is generally interpreted to represent a continuous differentiation process forming anhydrous and hydrous veins plus a cryptic enrichment in the surrounding peridotite. In order to constrain the mechanisms of vein formation and potentially clarify the nature and origin of the initial metasomatic agent, we performed a series of high-pressure experiments simulating the liquid line of descent of a basanitic magma differentiating within continental or mature oceanic lithosphere. This series of experiments has been conducted in an end-loaded piston cylinder apparatus starting from an initial hydrous ne-normative basanite at 1.5 GPa and temperature varying between 1,250 and 980°C. Near-pure fractional crystallization process was achieved in a stepwise manner in 30°C temperature steps and starting compositions corresponding to the liquid composition of the previous, higher-temperature glass composition. Liquids evolve progressively from basanite to peralkaline, aluminum-rich compositions without significant SiO₂ variation. The resulting cumulates are characterized by an anhydrous clinopyroxene + olivine assemblage at high temperature (1,250–1,160°C), while at lower temperature (1,130–980°C), hydrous cumulates with dominantly amphibole + minor clinopyroxene, spinel, ilmenite, titanomagnetite and apatite (1,130–980°C) are formed. This new data set supports the interpretation that anhydrous and hydrous metasomatic veins could be produced during continuous differentiation processes of primary, hydrous alkaline magmas at high pressure. However, the comparison between the cumulates generated by the fractional crystallization from an initial ne-normative liquid or from hy-normative initial compositions (hawaiite or picrobasalt) indicates that for all hydrous liquids, the different phases formed upon differentiation are mostly similar even though the proportions of hydrous versus anhydrous minerals could vary significantly. This suggests that the formation of amphibole-bearing metasomatic veins observed in the lithospheric mantle could be linked to the differentiation of initial liquids ranging from ne-normative to hy-normative in composition. The present study does not resolve the question whether the metasomatism observed in lithospheric mantle is a precursor or a consequence of alkaline magmatism; however, it confirms that the percolation and differentiation of a liquid produced by a low degree of partial melting of a source similar or slightly more enriched than depleted MORB mantle could generate hydrous metasomatic veins interpreted as a potential source for alkaline magmatism by various authors.     

Ultramafic and Mafic Inclusions from Adak Island: Crystallization History, and Implications for the Nature of Primary Magmas and Crustal Evolution in the Aleutian Arc

Xenolithic inclusions in calc-alkaline andesite from Mt. Moffettvolcano, Adak Island, Aleutian arc, reveal a nearly continuousrecord of crystallization of basaltic magmas in the crust, andpossibly upper mantle, of the arc. The record is more detailedand continuous than that obtained from study of calc-alkalinevolcanic rocks in the arc. Cumulate xenoliths form a progressiveseries in modal mineralogy from ultramafic, hornblende-bearingolivine clinopyroxenite to both hornblende-bearing and hornblende-freegabbros. The cumulate hornblende gabbro xenoliths are typicalof those found in island arc andesites worldwide. Xenolithicinclusions without cumulate textures, here termed compositexenoliths, are characterized by forsteritic olivine, zoned Cr-diopsideand hornblende, and are interpreted to have resulted from reactionand chilling upon magma mixing at depth. The olivine and clinopyroxene in both cumulate and compositexenoliths show the largest and the most complete variation trendsfor Ni, Cr, and FeO/MgO ratio yet reported in igneous xenolithsfrom island arc volcanic rocks. Variation of Ni in olivine indicatesthat the parent magmas for the xenoliths had minimum MgO contentsof 9 wt. per cent. Variation of Cr in clinopyroxene indicatesthat the magmas were basaltic rather than picritic, probablyin equilibrium with spinel lherzolite at near Moho depths. Successiveinjections of batches of primary melt into a magma chamber fractionatingolivine and clinopyroxene can reproduce observed compatibleelement depletion trends. A steady-state process of cotecticcrystallization in a magma chamber continually replenished withbasaltic magma is a possible mechanism for producing large accumulationsof olivine and clinopyroxene, suggesting that Alaskan-type ultramaficcomplexes are related to hydrous basaltic magmas in island arcs.This steady-state open-system crystallization process can alsoyield the abundant high-alumina basalt type in the Aleutianarc. Continued crystallization of high-alumina basalt in lowercrustal magma chambers, recorded in a mineralogically coherentseries of pyroxenite to hornblende gabbro xenoliths, can yieldbasaltic to andesitic magmas of the calc-alkaline series. No xenoliths with a sedimentary protolith have been found atMt Moffett, evidence that the arc crust is igneous in origin,with the lower crust formed of gabbro crystallized from mantle-derivedmelts. Ultramafic cumulates may reside in both the lower crustor upper mantle beneath the arc. A model is proposed wherebythe cumulate crystallization products of hydrous, mantle beneaththe arc. A model is define the upper mantle and lower crustof the arc over time.The net composition added to the crustof the arc is that of high-alumina basalt.     

Silica enrichment of Group II xenoliths by evolved alkali basalt from Jeju Island, South Korea: implication for modification of intraplate deep-seated rocks

Group II xenoliths, corresponding to the lithology of dunite, wehrlite to olivine clinopyroxenite and olivine websterite to websterite, occur in Pleisto-Holocene alkali basalts from Jeju Island, South Korea. The large grain size (up to 5?mm), moderate mg# [=100?×?Mg/(Mg?+?Fe_total) atomic ratio] of olivine (79–82) and pyroxenes (77–83), and absence of metamorphic textural features indicate that they are cumulates of igneous origin. Based on textural features, mineral equilibria and major and trace element variations, it can be inferred that the studied xenoliths were crystallized from basaltic melts enriched in incompatible trace elements and belong to the Jeju Pleisto-Holocene magma system. They appear to have been emplaced near the present Moho, an estimated 5–8?kbars beneath Jeju Island. Consolidation of cumulates was followed by infiltration of silica-enriched metasomatic melt, producing secondary orthopyroxenes at the expense of olivine. The metasomatic agent appears to have been a silica-enriched residual melt evolved from an initially slightly silica-undersaturated alkali basalt to silica-saturated compositions by fractional crystallization under relatively high pressure conditions. The result of this study indicates that relatively young olivine-bearing cumulates could have been metasomatized by a silica-enriched melt within underplates, suggesting that silica enrichment can occur in intraplate Moho-related rocks as well as in the upper mantle of the subarc area.     

Geochemistry of an Alaskan-type mafic-ultramafic complex in Eastern Desert,Egypt:New insights and constraints on the Neoproterozoic island arc magmatism

Mikbi intrusion(MI) is a part of the Neoproterozoic Nubian Shield located along the NE-SW trending major fracture zones prevailing southern Eastern Desert of Egypt. In this study, we present for the first time detailed mineralogical and bulk-rock geochemical data to infer some constraints on the parental magma genesis and to understand the tectonic processes contributed to MI formation. Lithologically, it is composed of fresh peridotite, clinopyroxenite, hornblendite, anorthosite, gabbronorite, pyroxene amphibole gabbro, amphibole gabbro and diorite. All rocks have low Th/La ratios(mostly <0.2) and lack positive Zr and Th anomalies excluding significant crustal contamination. They show very low concentrations of Nb, Ta, Zr and Hf together with sub-chondritic ratios of Nb/Ta(2-15) and Zr/Hf(19-35),suggesting that their mantle source was depleted by earlier melting extraction event. The oxygen fugacity(logfO_2) estimated from diorite biotite is around the nickel-nickel oxide buffer(NNO) indicating crystallization from a relatively oxidized magma. Amphiboles in the studied mafic-ultramafic rocks indicate relative oxygen fugacity(i.e. ΔNNO; nickel-nickel oxide) of 0.28-3 and were in equilibrium mostly with 3.77-8.24 wt.% H_2 O_melt(i.e. water content in the melt), consistent with the typical values of subduction-related magmas. Moreover, pressure estimates(0.53-6.79 kbar) indicate polybaric crystallization and suggest that the magma chamber(s) was located at relatively shallow crustal levels. The enrichment in LILE(e.g., Cs, Ba, K and Sr) and the depletion in HFSE(e.g., Th and Nb) relative to primitive mantle are consistent with island arc signature. The olivine, pyroxene and amphibole compositions also reflect arc affinity. These inferences suggest that their primary magma was derived from partial melting of a mantle source that formerly metasomatized in a subduction zone setting. Clinopyroxene and bulkrock data are consistent with orogenic tholeiitic affinity. Consequently, the mineral and bulk-rock chemistry strongly indicate crystallization from hydrous tholeiitic magma. Moreover, their trace element patterns are subparallel indicating that the various rock types possibly result from differentiation of the same primary magma. These petrological, mineralogical and geochemical characteristics show that the MI is a typical Alaskan-type complex.     

Olivine clinopyroxenite xenoliths in the Oslo Rift,SE Norway

Olivine clinopyroxenite xenoliths in a basalt flow at Krokskogen in the Oslo rift consist mainly of Al-Ti-rich clinopyroxene and alteration products after olivine (possibly also orthopyroxene). The clinopyroxene contains primary inclusions of Cr-Al-bearing titanomagnetite, pyrite and devitrified glass, and secondary fluid inclusions rich in CO₂. On the basis of petrography, mineral compositions and bulk major and trace element chemistry, it is concluded that the xenoliths represent cumulates with about 5% trapped liquid, formed from a mildly alkaline basaltic magma. Microthermometrical analysis of secondary or pseudosecondary fluid inclusions give a minimum pressure of formation of 5.5 to 6 kbars, that is a depth greater than 16–17 km. The host lava has initial _Nd=+4.16±0.17 and _Sr=–5.50±0.26, which is believed to reflect the isotopic composition of the lithospheric mantle source region under south Norway in early Permian time. The isotopic character of the magma which gave rise to the xenoliths is preserved in clinopyroxenes which have _Nd ^t =+1.9 to +2.6 and _Sr ^t = –1.1 to –1.8. The isotopic differences between the host magma and the xenoliths reflect some degree of crustal contamination of the xenolith's parent magma.The xenoliths of this study represent an important source of information about the large masses of dense cumulates found at depth in the crust under the Oslo rift.     

Chromite deposits in the northern Oman ophiolite: Mineralogical constraints

Chromite deposits in the northern Oman ophiolitic complex occur in three structural contexts, i.e., (1) at the base of the cumulate series, (2) in the top kilometer of the mantle sequence, and (3) in the deeper parts of the mantle. Types 1 and 2 are characterized by the diversity of interstitial silicates where in decreasing order of abundance olivine, clinopyroxene, orthopyroxene, plagioclase, and amphibole occur, as opposed to type 3 which contains only olivine. They differ however in ore texture. Similar silicates also occur as euhedral inclusions in chromite crystals, but their proportions are reversed. The composition of the interstitial silicates is comparable to that found in early cumulates. Type-1 and type-2 chromite deposits crystallized from a magma similar to that from which the basal cumulates formed (Al₂O₃, 15.1–16.1 wt%; FeO/MgO, 0.55–0.60). The type-3 chromites were derived from a magma of much lower Al₂O₃ content (12.5 wt%). It is considered that they belong to an older episode in the magmatic evolution of the complex.     

Thick sections of layered ultramafic cumulates in the Oman ophiolite revealed by an airborne hyperspectral survey: Petrogenesis and relationship to mantle diapirism

Using the HyMap instrument, we have acquired visible and near infrared hyperspectral data over the Maqsad area of the Oman ophiolite (~ 15 × 60 km). This survey allowed us to identify and map the distribution of clinopyroxene-rich cumulates (inter-layered clinopyroxenites and wehrlites) whose occurrence was previously undocumented in this area. The cumulates reach several hundred meters in thickness and crop out at distances exceeding 15 km on both sides of the Maqsad former spreading centre. They occur either in mantle harzburgites, as km-sized layered intrusions surrounded by fields of pegmatitic dykes consisting of orthopyroxene-rich pyroxenite and gabbronorites, or at the base of the crustal section where they are conformably overlain by cumulate gabbros. These ultramafic cumulates crystallized from silica- and Mg-rich melts derived from a refractory mantle source (e.g. high Cr#, low [Al₂O₃], low [TiO₂]). These melts are close to high-Ca boninites, although, strictly speaking, not perfect equivalents of present-day, supra-subduction zone, boninites. Chemical stratigraphy reveals cycles of replenishment, mixing and fractional crystallization from primitive (high Mg#) melts, typical of open magma chambers and migration of inter-cumulus melts. The TiO₂ content of clinopyroxene is always low (≤ 0.2 wt.%) but quite variable compared to the associated pegmatites that are all derived from a source ultra-depleted in high field strength elements (HFSE). This variability is not caused by fractional crystallization alone, and is best explained by hybridization between the ultra-depleted melts (parent melts of the pegmatites) and the less depleted mid-ocean ridge basalts (MORB) parent of the dunitic–troctolitic–gabbroic cumulates making up the crustal section above the Maqsad diapir.We propose that, following a period of magma-starved spreading, the Maqsad mantle diapir, impregnated with tholeiitic melts of MORB affinity, reached shallow depths beneath the ocean ridge. This diapir induced melting of the formerly accreted and hydrothermally altered lithosphere. At this stage, these boninitic-like lithospheric melts crystallized as pegmatitic dykes. As the diapir continued to rise, the amount of MORB reaching shallow depths increased, together with the surrounding temperature, leading to the formation of magma chambers where the crystallization of layered cumulates became possible. These cumulates remained rich in pyroxene and devoid of plagioclase as long as the contribution of MORB-derived melts was moderate relative to the lithospheric-derived melts. As the contribution of MORB to the refilling of the magma chamber increased, gabbroic cumulates started to crystallize.     

The andesite aqueduct: perspectives on the evolution of intermediate magmatism in west-central (105–99°W) Mexico

Intermediate calc-alkaline magma (52-65% SiO₂) in western-central Mexico is the focus of this paper, and the typically porphyritic andesites (57-65% SiO₂) form large central volcanoes, whereas basaltic andesites (52-57% SiO₂) are less porphyritic, and they are found as cones and flows but are absent from central volcanoes. Several studies of experimental phase equilibria on these lavas relate water concentration to the phenocryst assemblages and to the degree of crystallinity, so that the abundance, composition and variety of phenocrysts can be used to constrain the amount of water dissolved in the magmas. Thus, the plagioclase-rich andesites of Volcan Colima, Mexico, become so as a result of decompressional crystallisation at ~950 °C (the pyroxene phenocryst temperature), and lose their dissolved water (2.5 to 4.5 wt% H₂O) which is inversely proportional to the modal abundance of plagioclase. The feeding magma to V. Colima, North America's most productive central volcano, is represented by hornblende lamprophyre, a lava type without plagioclase phenocrysts which requires at least 6 wt% water to reproduce the phenocryst assemblage. Thus, degassing of the V. Colima magmas, and of those of the other central volcanoes in the western-central Mexican volcanic belt, contributes essentially all their dissolved water to the conduit or to the atmosphere. The source of this magmatic water is related to the source of the intermediate magmas. For some this must lie in the mantle, as the incorporation of hornblende-lherzolite nodules in a hydrous andesite with hornblende phenocrysts could only have occurred while ascending through the mantle. Consistent with a mantle source is the composition of the olivine phenocrysts in Mexican lavas with 10 to 5% MgO, which is in the mantle range of Fo_88-92. Accordingly, basaltic andesites and andesites with >5% MgO are candidates for a mantle source. The equilibration of intermediate magmas with the mantle, as illustrated by the experiments of various workers, requires that the magmas be hydrous at pressure. An additional constraint is that the activity of silica in the mantle must be equal to that in the hydrous magma at equilibrium. Using published and new experiments to define RTln%_SiO2 in hydrous liquids, this quantity is shown to vary as a function of liquid composition (H₂O, MgO, Na₂O+K₂O), and it approaches zero for quartz-saturated hydrous liquids. Using appropriate values of RTln%_SiO2 for three intermediate lavas, the amount of water required to equilibrate with an olivine-orthopyroxene mantle source is calculated, and within error indicates that only the most silica-rich magma is at water saturation in the mantle, in agreement with published experimental work. Hydrous intermediate magmas, ascending from their hornblende-lherzolite source regions (~1 to 1.5 GPa) along the hydrous adiabat, may not encounter any phase boundaries until 0.2-0.4 GPa because of the increase in the thermal stability of hornblende in water-undersaturated magmas. Therefore, the phenocryst assemblages of hornblende-free andesites equilibrate at low pressures. The virtual absence of basalt in west-central Mexico (<4 Ma) is considered to be related to the large increase in crystallinity found in isobaric hydrous experiments crystallising hornblende at pressures close to those at the base of the crust. As a large proportion of the ferromagnesian components of basalt is acceptable to hornblende, it does not take a significant cooling interval (~40-50 °C) below the liquidus for hydrous basaltic magma to acquire >50% crystallinity, evidently also an eruptible limit for V. Colima andesitic lavas. If the lower limit of water dissolved in Mexican intermediate magmas is accepted as that required for phenocryst equilibration (~6 wt% water), and the upper limit as saturation in the mantle source at 1 GPa (~16 wt%) then, with an estimate of the volcanic and plutonic magma delivery rate (km³/10⁶ year) per km of volcanic arc, the flux of water returned from the mantle along the 35,000-km, global subduction-related arc system can be estimated. Measurements of the volcanic flux are woefully few, and estimates from Mexico, the Lesser Antilles and central America show a range from 4 to 20 km³/10⁶ year2km which, if subtracted from the isotopically constrained continental growth rate, gives the plutonic flux rate. This suggests that, of the magma flux ascending to the continental crust, only about a fifth reaches the surface. If the dissolved magmatic water limits are coupled with the volcanic and plutonic emplacement rates, then the amount of water returned by magmatism to the crust is crudely in balance with that subducted.     

Petrology and geochemistry of mafic and ultramafic cumulate rocks from the eastern part of the Sabzevar ophiolite (NE Iran): Implications for their petrogenesis and tectonic setting

The Late Cretaceous Sabzevar ophiolite represents one of the largest and most complete fragments of Tethyan oceanic lithosphere in the NE Iran. It is mainly composed of serpentinized mantle peridotites slices; nonetheless, minor tectonic slices of all crustal sequence constituents are observed in this ophiolite. The crustal sequence contains a well-developed ultramafic and mafic cumulates section, comprising plagioclase-bearing wehrlite, olivine clinopyroxenite, olivine gabbronorite, gabbronorite, amphibole gabbronorite and quartz gabbronorite with adcumulate, mesocumulate, heteradcumulate and orthocumulate textures. The crystallization order for these rocks is olivine ​± ​chromian spinel → clinopyroxene → plagioclase → orthopyroxene → amphibole. The presence of primary magmatic amphiboles in the cumulate rocks shows that the parent magma evolved under hydrous conditions. Geochemically, the studied rock units are characterized by low TiO₂ (0.18–0.57 ​wt.%), P₂O₅ (<0.05 ​wt.%), K₂O (0.01–0.51 ​wt.%) and total alkali contents (0.12–3.04 ​wt.%). They indicate fractionated trends in the chondrite-normalized rare earth element (REE) plots and multi-element diagrams (spider diagrams). The general trend of the spider diagrams exhibit slight enrichment in large ion lithophile elements (LILEs) relative to high field strength elements (HFSEs) and positive anomalies in Sr, Pb and Eu and negative anomalies in Zr and Nb relative to the adjacent elements. The REE plots of these rocks display increasing trend from La to Sm, positive Eu anomaly (Eu/Eu1 ​= ​1.06–1.54) and an almost flat pattern from medium REE (MREE) to heavy REE (HREE) region [(Gd/Yb)_N ​= ​1–1.17]. Moreover, clinopyroxenes from the cumulate rocks have low REE contents and show marked depletion in light REE (LREE) compared to MREE and HREE [(La/Sm)_N ​= ​0.10–0.27 and (La/Yb)_N ​= ​0.08–0.22]. The composition of calculated melts in equilibrium with the clinopyroxenes from less evolved cumulate samples are closely similar to island arc tholeiitic (IAT) magmas. Modal mineralogy, geochemical features and REE modeling indicate that Sabzevar cumulate rocks were formed by crystal accumulation from a hydrous depleted basaltic melt with IAT affinity. This melt has been produced by moderate to high degree (~15%) of partial melting a depleted mantle source, which partially underwent metasomatic enrichment from subducted slab components in an intra-oceanic arc setting.     

A mineral and cumulate perspective to magma differentiation at Nisyros volcano,Aegean arc

Lavas and pyroclastic products of Nisyros volcano (Aegean arc, Greece) host a wide variety of phenocryst and cumulate assemblages that offer a unique window into the earliest stages of magma differentiation. This study presents a detailed petrographic study of lavas, enclaves and cumulates spanning the entire volcanic history of Nisyros to elucidate at which levels in the crust magmas stall and differentiate. We present a new division for the volcanic products into two suites based on field occurrence and petrographic features: a low-porphyricity andesite and a high-porphyricity (rhyo)dacite (HPRD) suite. Cumulate fragments are exclusively found in the HPRD suite and are predominantly derived from upper crustal reservoirs where they crystallised under hydrous conditions from melts that underwent prior differentiation. Rarer cumulate fragments range from (amphibole-)wehrlites to plagioclase-hornblendites and these appear to be derived from the lower crust (0.5–0.8 GPa). The suppressed stability of plagioclase and early saturation of amphibole in these cumulates are indicative of high-pressure crystallisation from primitive hydrous melts (≥ 3 wt% H₂O). Clinopyroxene in these cumulates has Al₂O₃ contents up to 9 wt% due to the absence of crystallising plagioclase, and is subsequently consumed in a peritectic reaction to form primitive, Al-rich amphibole (Mg# > 73, 12–15 wt% Al₂O₃). The composition of these peritectic amphiboles is distinct from trace element-enriched interstitial amphibole in shallower cumulates. Phenocryst compositions and assemblages in both suites differ markedly from the cumulates. Phenocrysts, therefore, reflect shallow crystallisation and do not record magma differentiation in the deep arc crust.     

Fluid-Inclusion Evidence for an Upper-Mantle Origin for Green Clinopyroxenes in Late Cenozoic Basanites from the Nógrád-Gömör Volcanic Field,Northern Hungary/Southern Slovakia

Green clinopyroxenes with elevated Fe and Na contents coexist with “normal” clinopyroxene phenocrysts in alkali basalts from the Nógrád-Gömör Volcanic Field (NGVF) of northern Hungary and southern Slovakia. The coexistence of these clinopyroxenes with incompatible compositions in the same sample is often used as evidence for mixing between a mafic and a more evolved melt. However, results of fluid-inclusion, textural, and geochemical studies of samples from Tertiary basanites from the NGVF suggest that the majority of the green clinopyroxenes could not have formed from magma mixing but, rather, are products of lithospheric processes such as metasomatism or dynamic melt flow.

Two distinct types of green clinopyroxenes have been identified. Group 1 green clinopyroxenes are Al rich and contain CO₂ inclusions; Group 2 green clinopyroxenes are Al poor and lack CO₂ inclusions. On the basis of analysis of CO₂ inclusions, the Group 1 clinopyroxenes, observed as xenocrysts and major constituents of clinopyroxenite xenoliths, were entrained into the host basanitic magmas in the uppermost mantle. These clinopyroxenes originally formed during a meta-somatic event or as a result of dynamic melt flow in the mantle. Group 2 clinopyroxenes likely represent xenocrysts from disaggregated dioritic cumulates produced from melt(s) related to the host basanitic magmas.     

苏鲁超高压变质带胡家林超镁铁质岩成因及构造意义

胡家林超镁铁质杂岩体产于苏鲁超高压变质带中部,纯橄岩和(石榴)单斜辉石岩呈不连续透镜体产于蛇纹石化橄榄岩中。纯橄岩遭受了部分蛇纹石化(烧失量=6.6%～13.2%),全岩富集强相容元素(Ni、Cr、Co)和Ir族PGE(IPGE;Ir、Os、Ru)及高IPGE/PPGE值,亏损Al、Ti、V,具高Mg~#橄榄石(Fo=91.7～92.4)和高Cr~#(0.68～0.76)尖晶石。纯橄岩高耐熔地球化学及矿物化学特征和古老的大陆岩石圈地幔相一致,表明其原岩来源于弧前地幔,代表了华北克拉通古老的大陆岩石圈地幔残留。(石榴)单斜辉石岩全岩呈相对低含量的强相容元素(Cr、Ni、Co)和IPGE,高含量的Al、Ti、V和流体迁移元素(Sr、Pb和Ba),球粒陨石标准化REE配分图呈明显"上凸"型,具低Mg~#橄榄石(Fo=76.6～76.8)和低Al_2O_3(2.76%)和高SiO_2(54.56%～56.87%)的单斜辉石。全岩组成和矿物化学表明其原岩为俯冲带内超镁铁质火成堆晶岩,最初岩浆由地幔岩高程度部分熔融的熔体和俯冲带中富H_2O流体和/或熔体构成。(石榴)单斜辉石岩原岩曾被地幔流带入扬子大陆俯冲板片和上覆地幔楔之间的俯冲通道,经历了超高压变质作用和生成大量石榴石。(石榴)单斜辉石岩在折返过程中,与大陆岩石圈地幔楔剥离的蛇纹石化橄榄岩及纯橄岩相结合,形成超镁铁质杂岩体,整体被低密度的俯冲板片(主要由花岗质片麻岩和变质沉积岩组成)裹挟,折返至地壳浅部。     

Petrogenesis of the Piqiang mafic-ultramafic layered intrusion and associated Fe-Ti-V oxide deposit in Tarim Large Igneous Province,NW China

ABSTRACT

The Piqiang intrusion is one of the two important ma?c-ultrama?c layered intrusions that host giant Fe-Ti-V oxide deposits in the Permian Tarim Large Igneous Province, NW China. The intrusion mainly consists of gabbro, anorthosite and minor plagioclase-bearing clinopyroxenite in the marginal zone. Disseminated to massive Fe-Ti oxide ores occur as layers and lenses within the gabbro. SHRIMP zircon U-Pb results from both a gabbro from the Piqiang intrusion and a granite from the surrounding granitic dyke yield ages of ~270 Ma. Geochemically, the Piqiang silicate rocks are enriched in light rare earth elements (LREE) and large ion lithophile elements (LILE), moderately depleted in high ?eld strength elements (HFSE), and have a limited range of Sr-Nd-Hf isotopic compositions. The similar mineralogy, mineral compositions, and trace element characteristics of the layered units suggest that all the rocks are co-magmatic. The parental magma is Fe-Ti-rich and is akin to the most primitive diabasic dyke which is associated with the Piqiang intrusion. Partial melting of the Tarim mantle plume with involvement of a subduction-metasomatized lithospheric mantle source best explains the geochemistry and petrogenesis of the parental magmas of the Piqiang intrusion. We propose that the lithospheric mantle source may have been metasomatized by subduction-related materials and the metasomatic enrichment of this source region which may be correlated with oceanic sediment recycling during southward subduction of the South Tianshan oceanic slab during the Early-Middle Paleozoic. Crystal settling and mechanical sorting is the predominant process responsible for the formation of the massive Fe-Ti oxide ores in the Piqiang intrusion. Central to ore formation is a combination of the protracted differentiation history of a Fe-Ti-enriched parental magma and the later addition of external H₂O from the country rocks to the slowly cooling magma chamber.     

Growth of subcontinental lithosphere: evidence from repeated dike injections in the Balmuccia lherzolite massif, Italian Alps

The Balmuccia alpine lherzolite massif is a fragment of subcontinental lithospheric mantle emplaced into the lower crust 251 Ma ago during the final, extensional phase of the Hercynian orogeny. The Balmuccia massif consists largely of lherzolite, with subordinate harzburgite and dunite, and an array of dike rocks formed in the mantle before crustal emplacement. Dike rocks include websterite and bronzitite of the Cr-diopside suite, spinel clinopyroxenite and spinel-poor websterite of the Al-augite suite, gabbro and gabbronorite of the late gabbro suite, and hornblendite of the hydrous vein suite. The dike rocks display consistent intrusive relationships with one another, such that Cr-diopside suite dikes are always older than dikes and veins of the Al-augite suite, followed by dikes of the late gabbro suite and veins of the hydrous vein suite. Phlogopite (phl) veinlets that formed during interaction with the adjacent crust are the youngest event. There are at least three generations of Cr-diopside suite dikes, as shown by crosscutting relations. Dikes of the Al-augite suite form a polybaric fractionation series from spinel clinopyroxenite to websterite and feldspathic websterite, which crystallized from aluminous alkaline magmas at relatively high pressures. The late gabbro suite of dikes intruded at lower pressures, where plagioclase saturation occurred before significant mafic phase fractionation. Hornblendite veins have distinct compositional and isotopic characteristics, which show that they are not related to either the Al-augite suite or to the late gabbro dike suite. Cr-diopside suite dikes have Nd and Sr isotopic compositions similar to those of the host lherzolite and within the range of compositions defined by ocean–island basalts. The Al-augite dikes and the hornblendite veins have Sr and Nd isotopic compositions similar to those of Cr-diopside suite lherzolite and websterite. The late gabbro dikes have Nd and Sr isotopic compositions similar to mid-ocean ridge basalt (MORB) asthenosphere. Lead isotopic compositions for all of the samples fall in the present-day MORB field on the ²⁰⁸Pb/²⁰⁴Pb vs. ²⁰⁶Pb/²⁰⁴Pb diagram but are displaced above this field on the ²⁰⁷Pb/²⁰⁴Pb vs. ²⁰⁶Pb/²⁰⁴Pb diagram. There is overlap in the data between the Cr-diopside suite and the Al-augite and hydrous vein suites, with the exception that the Cr-diopside websterite dikes have more radiogenic Pb than any of the other samples. In Pb–Pb space as well, the late gabbro suite has the least radiogenic isotopic compositions, reflecting a change in magma source region during uplift. These data show that tectonic thinning of subcontinental lithospheric mantle during extension caused a change in the source regions of mantle-derived magmas from an ocean island basalt (OIB)-like lithosphere to the underlying MORB asthenosphere. They also demonstrate that the upper mantle acquires its heterogeneous isotopic character through several different processes, including in situ radiogenic growth, addition of asthenospheric melts, dike-wall rock ionic exchange, redistribution of the lithospheric dike and vein materials by melting, and in the late stages of emplacement, assimilation of crustal materials.     

Two magmatic series with island arc affinities within the vourinos ophiolite

Within the Vourinos ophiolite evidence of two magmatic series has been preserved in cognate cumulates and in effusive and hypabyssal rocks, which constitute the earlier Krapa sequence and the younger Asprokambo sequence. The Asprokambo dyke basic magmas which are poor in incompatible elements and relatively Ni and Cr rich, bear some resemblance to very low Ti basalts (transitional to boninites) found in subduction related arcs or interarc basins. Krapa series magmas from sills, massive and pillow lavas are best equated with low-K tholeiites of island arc suites. Compositions of Al- and Ti- poor Cpx in lavas from both series are comparable to those in island arc basalts, the Asprokambo Cpx being richer in Ca and Cr than those from Krapa.The large volume of cumulates from the Krapa sequence displays the following crystallization order: Ol±Sp, Cpx, Pl±Opx, Mt. Periodic influx of fresh magma batches into the magma chamber occurred mainly during the formation of the lower cumulates (wehrlite, Ol-clinopyroxenite and melagabbro). The upper cumulates, gabbronorite and leucogabbronorite with minor Mt-bearing gabbronorite, crystallized in the upper levels of a magma chamber which became progressively smaller with time. In the Asprokambo sequence, Ol+Sp, Opx, Cpx, PI and Amph are the successively crystallizing phases. The ortho to heteradcumulates consist of websterite, Pl-websterite, gabbronorite, amphibole bearing leuconorite, diorite and granophyre. In cumulates, especially in the lower Krapa sequence, significant subsolidus reaction was probably induced by the persistence of high geothermal gradients linked to continuous magmatism. Petrological features indicate that the evolution of the Krapa series is more compatible with an intermediate fractional/equilibrium crystallization history in an initially open system, whereas nearly perfect fractional crystallization in closed system may have occurred in the small Asprokambo magma chambers. Chemical variations in the lavas of both series can be explained in terms of crystallization of the observed cumulates. Significantly, the Asprokambo intrusives have igneous Mg-hornblende and vanadium bearing, chromian, aluminous titaniferous magnetite, crystallization of which is responsible for the calcalkaline evolutionary trend of these rocks. Major and trace element modelling necessitates a two stage model for the petrogenesis of the Vourinos parental melts, involving high-degree remelting of previously depleted mantle sources favoured by the influx of subduction derived hydrous fluids. The primary magmas parental to the Krapa and Asprokambo series could have been derived respectively by 20 and 30% equilibrium partial fusion of variably depleted lherzolitic sources, leaving residua having a harzburgitic to dunitic composition.     

Redox evolution of differentiating hydrous basaltic magmas recorded by zircon and apatites in mafic cumulates: The case of the Malayer Plutonic Complex,Western Iran

Mafic-ultramafic cumulates can provide records of basaltic magma chambers' conditions and processes, which are often difficult to determine in areas dominated by crustal-derived felsic intrusions, such as the Malayer Plutonic Complex (MPC), Western Iran. New U-Pb zircon ages for mafic cumulates in the MPC confirm the presence of isolated magma chambers of contrasting compositions during Middle Jurassic. Mafic cumulates found in seven separate zones across the MPC vary from olivine gabbro to anorthosite. While the mineralogical, textural, and geochemical lines of evidence recorded in mafic cumulates indicate pH₂O controls on the liquidus phases, the estimated oxygen fugacity (logfO₂) using zircon and apatite chemistry suggests a smoothly rising redox state during the fractionation process, consistent with the trend expected for late-stages differentiation of hydrous arc magmas. This trend is further confirmed by sulfur speciation in apatites determined from microbeam sulfur K-edge X-ray absorption near edge structure (μ-XANES) spectra (S⁶⁺/∑S = 0.93–0.98 ~ FMQ + 2 to 0.99 ~ FMQ + 3, where ∑S = S⁶⁺+S⁴⁺+S²⁻). The low S content and increasing redox state of the fractionating basaltic melts most likely resulted from preferential removal of sulfur en-route to the magma chambers along with effective assimilation of oxidizing crustal components. The reduced condition in the early basaltic melt is also evidenced by the presence of pyrite and magnetite inclusions in olivines in mafic cumulates. The shift in the prevailing fO₂ from sulfide-saturated to sulfate-bearing recorded by MPC mafic cumulates, similar to that in other magmatic arcs, is accompanied by changes in the differentiation path from transitional tholeiitic to calc-alkaline.     

徐淮地区中生代深部地壳的物质组成及热状态——深源捕虏体证据

徐淮地区中生代侵入杂岩中含有丰富的深源岩石捕虏体,包括榴辉岩类、单斜辉石岩、角闪岩类和片麻岩类。深源捕虏体的岩相学研究表明,它们经历了早期的榴辉岩相变质和晚期的角闪岩相退化变质,然后被寄主岩浆所捕获。捕虏体中矿物平衡温压估算结果显示,榴辉岩相变质的温压条件为:T=657～992℃,P=1.33～2.78GPa,所反映的地温梯度介于克拉通地温(40mW/m2)和大洋地温(60mW/m2)之间;晚期角闪岩相退变的温压条件为:T=523～878℃,P=0.5～1.02GPa,这与中国东部新生代地温梯度相一致。本区中生代深部地壳主要由一套混杂堆积岩所构成,包括退变榴辉岩、退变石榴辉石岩、角闪岩类和片麻岩类。该区深源捕虏体的P-T演化暗示中生代早期华北地块东部深部地壳和/或岩石圈地幔曾存在一次重要的加厚过程;苏鲁造山带的形成可能是扬子地块沿北西方向俯冲于华北地块之下的产物;中生代郯庐断裂带并不存在巨大左行平移。     

Highly refractory Archaean peridotite cumulates:Petrology and geochemistry of the Seqi Ultramafic Complex,SW Greenland

This paper investigates the petrogenesis of the Seqi Ultramafic Complex, which covers a total area of approximately 0.5 km~2. The ultramafic rocks are hosted by tonalitic orthogneiss of the ca. 3000 Ma Akia terrane with crosscutting granitoid sheets providing an absolute minimum age of 2978 ± 8 Ma for the Seqi Ultramafic Complex. The Seqi rocks represent a broad range of olivine-dominated plutonic rocks with varying modal amounts of chromite, orthopyroxene and amphibole, i.e. various types of dunite(s.s.),peridotite(s.l.), as well as chromitite. The Seqi Ultramafic Complex is characterised primarily by refractory dunite, with highly forsteritic olivine with core compositions having Mg# ranging from about 91 to 93. The overall high modal contents, as well as the specific compositions, of chromite rule out that these rocks represent a fragment of Earth's mantle. The occurrence of stratiform chromitite bands in peridotite, thin chromite layers in dunite and poikilitic orthopyroxene in peridotite instead supports the interpretation that the Seqi Ultramafic Complex represents the remnant of a fragmented layered complex or a magma conduit, which was subsequently broken up and entrained during the formation of the regional continental crust.Integrating all of the characteristics of the Seqi Ultramafic Complex points to formation of these highly refractory peridotites from an extremely magnesian(Mg# ~ 80), near-anhydrous magma, as olivinedominated cumulates with high modal contents of chromite. It is noted that the Seqi cumulates were derived from a mantle source by extreme degrees of partial melting(40%). This mantle source could potentially represent the precursor for the sub-continental lithospheric mantle(SCLM) in this region,which has previously been shown to be ultra-depleted. The Seqi Ultramafic Complex, as well as similar peridotite bodies in the Fiskefjord region, may thus constitute the earliest cumulates that formed during the large-scale melting event(s), which resulted in the ultra-depleted cratonic keel under the North Atlantic Craton. Hence, a better understanding of such Archaean ultramafic complexes may provide constraints on the geodynamic setting of Earth's first continents and the corresponding SCLM.     

The age of Dar al Gani 476 and the differentiation history of the martian meteorites inferred from their radiogenic isotopic systematics

Samarium-neodymium isotopic analysis of the martian meteorite Dar al Gani 476 yields a crystallization age of 474 ± 11 Ma and an initial ε_Nd¹⁴³ value of +36.6 ± 0.8. Although the Rb-Sr isotopic system has been disturbed by terrestrial weathering, and therefore yields no age information, an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.701249 ± 33 has been estimated using the Rb-Sr isotopic composition of the maskelynite mineral fraction and the Sm-Nd age. The Sr and Nd isotopic systematics of Dar al Gani 476, like those of the basaltic shergottite QUE94201, are consistent with derivation from a source region that was strongly depleted in incompatible elements early in the history of the solar system. Nevertheless, Dar al Gani 476 is derived from a source region that has a slightly greater incompatible enrichment than the QUE94201 source region. This is not consistent with the fact that the parental magma of Dar al Gani 476 is significantly more mafic than the parental magma of QUE94201, and underscores a decoupling between the major element and trace element-isotopic systematics observed in the martian meteorite suite.Combining the ε_Nd¹⁴²-ε_Nd¹⁴³ isotopic systematics of the martian meteorites yields a model age for planetary differentiation of 4.513_+0.033^−0.027 Ga. Using this age, the parent/daughter ratios of martian mantle sources are calculated assuming a two-stage evolutionary history. The calculated sources have very large ranges of parent/daughter ratios (⁸⁷Rb/⁸⁶Sr = 0.037-0.374; ¹⁴⁷Sm/¹⁴⁴Nd = 0.182-0.285; ¹⁷⁶Lu/¹⁷⁷Hf = 0.028-0.048). These ranges exceed the ranges estimated for terrestrial basalt source regions, but are very similar to those estimated for the sources of lunar mare basalts. In fact, the range of parent/daughter ratios calculated for the martian meteorite sources can be produced by mixing between end-members with compositions similar to lunar mare basalt sources. Two of the sources have compositions that are similar to olivine and pyroxene-rich mafic cumulates with variable proportions of a Rb-enriched phase, such as amphibole, whereas the third source has the composition of liquid trapped in the cumulate pile (i.e. similar to KREEP) after ∼99% crystallization. Correlation between the proportion of trapped liquid in the meteorite source regions and estimates of f_O2, suggest that the KREEP-like component may be hydrous. The success of these models in reproducing the martian meteorite source compositions suggests that the variations in trace element and isotopic compositions observed in the martian meteorites primarily reflect melting of the crystallization products of an ancient magma ocean, and that assimilation of evolved crust by mantle derived magmas is not required. Furthermore, the decoupling of major element and trace element-isotopic systematics in the martian meteorite suite may reflect the fact that trace element and isotopic systematics are inherited from the magma source regions, whereas the major element abundances are limited by eutectic melting processes at the time of magma formation. Differences in major element abundances of parental magma, therefore, result primarily from fractional crystallization after leaving their source regions.