Interaction between protokimberlite melts and mantle lithosphere: Evidence from mantle xenoliths from the Dalnyaya kimberlite pipe,Yakutia (Russia)

The Dalnyaya kimberlite pipe(Yakutia,Russia) contains mantle peridotite xenoliths(mostly Iherzolites and harzburgites) that show both sheared porphyroclastic(deformed) and coarse granular textures,together with ilmenite and clinopyroxene megacrysts.Deformed peridotites contain high-temperature Fe-rich clinopyroxenes,sometimes associated with picroilmenites,which are products of interaction of the lithospheric mantle with protokimberlite related melts.The orthopyroxene-derived geotherm for the lithospheric mantle beneath Dalnyaya is stepped similar to that beneath the Udachnaya pipe.Coarse granular xenoliths fall on a geotherm of 35 mWm-2 whereas deformed varieties yield a 45 mWm-2)geotherm in the 2-7.5 GPa pressure interval.The chemistry of the constituent minerals including garnet,olivine and clinopyroxene shows trends of increasing Fe~#(=Fe/(Fe+Mg))with decreasing pressure.This may suggest that the interaction with fractionating protokimberlite melts occurred at different levels.Two major mantle lithologies are distinguished by the trace element patterns of their constituent minerals,determined by LA-ICP-MS.Orthopyroxenes,some clinopyroxenes and rare garnets are depleted in Ba,Sr,HFSE and MREE and represent relic lithospheric mantle.Re-fertilized garnet and clinopyroxene are more enriched.The distribution of trace elements between garnet and clinopyroxene shows that the garnets dissolved primary orthopyroxene and clinopyroxene.Later high temperature clinopyroxenes related to the protokimberlite melts partially dissolved these garnets.Olivines show decreases in Ni and increases in Al,Ca and Ti from Mg-rich varieties to the more Fe-rich,deformed and refertilized ones.Minerals showing higher Fe~#(0.11-0.15) are found within intergrowths of low-Cr ilmenite-clinopyroxene-garnet related to the crystallization of protokimberlite melts in feeder channels.In P-f(O_2) diagrams,garnets and Cr-rich clinopyroxenes indicate reduced conditions at the base of the lithosphere at-5 log units below a FMQ buffer.However,Cr-poor clinopyroxenes,together with ilmenite and some Fe-Ca-rich garnets,demonstrate a more oxidized trend in the lower part of lithosphere at-2 to 0 log units relative to FMQ.Clinopyroxenes from xenoliths in most cases show conditions transitional between those determined for garnets and megacrystalline Cr-poor suite.The relatively low diamond grade of Dalnyaya kimberlites is explained by a high degree of interaction with the oxidized protokimberlite melts,which is greater at the base of the lithosphere.     

Insights into Li and Li isotope cycling and sub-arc metasomatism from veined mantle xenoliths,Kamchatka

Harzburgitic xenoliths cut by pyroxenite veins from Avachinsky volcano, Kamchatka, are derived from the sub-arc mantle and record element transfer from the slab to the arc. Olivine and orthopyroxene in the harzburgites have Li isotopic compositions (δ⁷Li = +2.8 to +5.6) comparable to estimates of the upper mantle (δ⁷Li ~ +4 ± 2). The pyroxenite veins, which represent modal metasomatism and may therefore provide information about the metasomatic agent, have mantle-normalized trace element characteristics that suggest overprinting of their mantle source by an aqueous, slab-derived fluid. These include relative enrichments of Pb over Ce, U over Th and Sr over Nd. Li is enriched relative to the HREE, and ortho- and clinopyroxene from the veins are in Li elemental and isotopic equilibrium with each other and the surrounding harzburgite. Vein samples (δ⁷Li = +3.0 to +5.0) do not record a significant slab-derived δ⁷Li signature. These observations can be reconciled if slab Li diffusively re-equilibrates in the mantle wedge. Modeling demonstrates that Li equilibration of small (1–2 cm width) veins or melt conduits is achieved at mantle wedge temperatures within 10¹–10⁵ years. We conclude that strongly fractionated Li isotopic signatures cannot be sustained for long periods in the sub-arc mantle, at least at shallow (<70 km) depths. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Pyroxenite xenoliths from Marsabit (Northern Kenya): evidence for different magmatic events in the lithospheric mantle and interaction between peridotite and pyroxenite

Garnet-bearing and garnet-free pyroxenite xenoliths from Quaternary basanites of Marsabit, northern Kenya, were analysed for microstructures and mineral compositions (major and trace elements) to constrain the thermal and compositional evolution of the lithospheric mantle in this region. Garnet-bearing rocks are amphibole-bearing websterite with ~5–10 vol% orthopyroxene. Clinopyroxene is LREE-depleted and garnet has high HREE contents, in agreement with an origin as cumulates from basaltic mantle melts. Primary orthopyroxene inclusions in garnet suggest that the parental melts were orthopyroxene-saturated. Rock fabrics vary from weakly to strongly deformed. Thermobarometry indicates extensive decompression and cooling (~970–1,100°C at ~2.3–2.6 GPa to ~700–800°C at ~0.5–1.0 GPa) during deformation, best interpreted as pyroxenite intrusion into thick Paleozoic continental lithosphere subsequently followed by continental rifting (i.e., formation of the Mesozoic Anza Graben). During continental rifting, garnet websterites were decompressed (garnet-to-spinel transition) and experienced the same P–T evolution as their host peridotites. Strongly deformed samples show compositional overlaps with cpx-rich, initially garnet-bearing lherzolite, best explained by partial re-equilibration of peridotite and pyroxenite during deformation and mechanical mingling. In contrast, garnet-free pyroxenites include undeformed, cumulate-like samples, indicating that they are younger than the garnet websterites. Major and trace element compositions of clinopyroxene and calculated equilibrium melts suggest crystallisation from alkaline basaltic melt similar to the host basanite, which suggests formation in the context of alkaline magmatism during the development of the Kenya rift. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Spinel lherzolite xenoliths from the Premier kimberlite (Kaapvaal craton, South Africa): Nature and evolution of the shallow upper mantle beneath the Bushveld complex

Coarse-grained, granular spinel lherzolites xenoliths from the Premier kimberlite show evidence of melt extraction and metasomatic enrichment, documenting a complex history for the shallow mantle beneath the Bushveld complex. Compositions of orthopyroxene, clinopyroxene and spinel indicate equilibration within the spinel–peridotite facies of the upper mantle, at depths from 80 to 100 km and temperatures from 720 to 850 °C. Bulk compositions have lower Mg-number [atomic 100 Mg/(Mg + Fe*)] than previously studied spinel peridotites from Premier, and have higher Mg/Si than low-temperature coarse grained garnet lherzolites, suggesting shallower melting conditions or metasomatic enrichment. Clinopyroxene in one sample is highly LREE-depleted indicating very minor modification of a residue of 20% melt extraction, whereas the calculated REE pattern for a melt in equilibrium with a mildly LREE-depleted sample is similar to MORB or late Archean basalt, possibly related to the Bushveld Complex. Bulk and mineral compositions suggest minimal refertilization by silicate melts in four out of six samples, but REE patterns indicate introduction of a LIL-enriched component that may be related to kimberlite.     

Immiscibility between calciocarbonatitic and silicate melts and related wall rock reactions in the upper mantle: a natural case study from Romanian mantle xenoliths

This paper presents the textural, mineralogical and chemical study of veinlets cross-cutting peridotite xenoliths from the lithospheric mantle and brought to the surface by alkaline basalts (Persani Mountains, Romania). The veinlets utilized pre-existing zones of weakness in the host rocks or display a random distribution, lining grain boundaries or cross-cutting any mineral, and always forming an interconnected network. They are filled with carbonate patches included in a silicate matrix. Both products are holocrystalline. Carbonate products have alkali-poor calciocarbonatitic to sövitic compositions, while the silicate matrix composition ranges from monzodioritic to monzonitic and alkali feldspar syenitic, depending on the host-sample, i.e., within a rather alkaline silica-saturated series. The mineral phases present in the silicate matrix (F-apatite, armalcolite, chromite, diopside–enstatite series, plagioclase–sanidine series) are usually present in the carbonate zones, where forsterite is also found. Some minerals cross-cut the interface between both types of zones. Only the matrix is different, feldspathic (oligoclase to sanidine) in the former and pure calcite in the latter. Thus, mineralogical and textural relationships between both products are consistent with an origin with equilibrium liquid immiscibility. Mantle minerals cross-cut by veinlets are sometimes resorbed at grain boundaries, and at the contact of the most alkaline silicate and carbonate melts, subhedral diopside/augite formed at the expense of mantle enstatite or olivine. In terms of mineral chemistry, the compositional variations recorded by vein minerals vary along a continuous trend. They generally superpose to those observed from lherzolites to harzburgites, and exhibit the same range of composition as that observed between rims and cores of mantle minerals cross-cut by veinlets. In detail, the Ca-rich pyroxenes of veinlets are Al-poor and Mg-rich; cpx in the carbonate zones are slightly more Ca-rich than those in the silicate matrix; spinels are relatively Al- and Mg-poor but rather Cr- and Fe-rich. Existence of only one titanium oxide (armalcolite) and various pairs of pyroxenes suggest crystallization temperatures in the range 1100–1200°C and pressures between 10–15 kb. Feldspar compositions in silicate materials, which vary continuously from labradorite to sanidine, are consistent with hypersolvus and dry crystallization conditions. All of these results provide evidence that immiscibility occurred at mantle depth as the liquid was forcibly injected during hydraulic fracturing of the mantle. The compositions of conjugate melts suggest a very large miscibility gap, as expected at high pressure in a dry environment from the experiments of Kjarsgaard and Hamilton [Kjarsgaard, B.A., Hamilton, D.L., 1988. Liquid immiscibility and the origin of alkali-poor carbonatites. Mineral. Mag. 52, 43–55; Kjarsgaard, B.A., Hamilton, D.L., 1989. The genesis of carbonatites by immiscibility. In: Bell, K. (Ed.), Carbonatites: Genesis and Evolution. Unwyn Hyman, London, pp. 388–404.]. The parental melt was carbonate, silica-undersaturated and rich in F, Cl and CO₂. Both immiscible melts were water-undersaturated. The cooling rate until total crystallization in veinlets was very slow, limited and necessarily occurred at mantle depth. Wall rock reactions leading to the formation of Ca-rich pyroxene at the expense of mantle enstatite or olivine occurred only at the contact with somewhat alkali-rich carbonatitic or silicate melts. Calcite, always anhedral, is the last mineral to crystallize. It is a differentiation product formed by magmatic crystallization or wall rock reaction. In some cases, given the rarity of any other minerals, it may be the product of the crystallization of a pure sövite immiscible melt.     

Phlogopite in mantle xenoliths and kimberlite from the Grib pipe,Arkhangelsk province,Russia:Evidence for multi-stage mantle metasomatism and origin of phlogopite in kimberlite

We present petrography and mineral chemistry for both phlogopite,from mantle-derived xenoliths(garnet peridotite,eclogite and clinopyroxene-phlogopite rocks)and for megacryst,macrocryst and groundmass flakes from the Grib kimberlite in the Arkhangelsk diamond province of Russia to provide new insights into multi-stage metasomatism in the subcratonic lithospheric mantle(SCLM)and the origin of phlogopite in kimberlite.Based on the analysed xenoliths,phlogopite is characterized by several generations.The first generation(Phil)occurs as coarse,discrete grains within garnet peridotite and eclogite xenoliths and as a rock-forming mineral within clinopyroxene-phlogopite xenoliths.The second phlogopite generation(Phl2)occurs as rims and outer zones that surround the Phil grains and as fine flakes within kimberlite-related veinlets filled with carbonate,serpentine,chlorite and spinel.In garnet peridotite xenoliths,phlogopite occurs as overgrowths surrounding garnet porphyroblasts,within which phlogopite is associated with Cr-spinel and minor carbonate.In eclogite xenoliths,phlogopite occasionally associates with carbonate bearing veinlet networks.Phlogopite,from the kimberlite,occurs as megacrysts,macrocrysts,microcrysts and fine flakes in the groundmass and matrix of kimberlitic pyroclasts.Most phlogopite grains within the kimberlite are characterised by signs of deformation and form partly fragmented grains,which indicates that they are the disintegrated fragments of previously larger grains.Phil,within the garnet peridotite and clinopyroxene-phlogopite xenoliths,is characterised by low Ti and Cr contents(TiO_21 wt.%,Cr_2 O_31 wt.% and Mg# = 100 × Mg/(Mg+ Fe)92)typical of primary peridotite phlogopite in mantle peridotite xenoliths from global kimberlite occurrences.They formed during SCLM metasomatism that led to a transformation from garnet peridotite to clinopyroxene-phlogopite rocks and the crystallisation of phlogopite and high-Cr clinopyroxene megacrysts before the generation of host-kimberlite magmas.One of the possible processes to generate low-Ti-Cr phlogopite is via the replacement of garnet during its interaction with a metasomatic agent enriched in K and H_2O.Rb-Sr isotopic data indicates that the metasomatic agent had a contribution of more radiogenic source than the host-kimberlite magma.Compared with peridotite xenoliths,eclogite xenoliths feature low-Ti phlogopites that are depleted in Cr_2O_3 despite a wider range of TiO_2 concentrations.The presence of phlogopite in eclogite xenoliths indicates that metasomatic processes affected peridotite as well as eclogite within the SCLM beneath the Grib kimberlite.Phl2 has high Ti and Cr concentrations(TiO_22 wt.%,Cr_2O_31 wt.% and Mg# = 100× Mg/(Mg + Fe)92)and compositionally overlaps with phlogopite from polymict brecc:ia xenoliths that occur in global kimberlite formations.These phlogopites are the product of kimberlitic magma and mantle rock interaction at mantle depths where Phl2 overgrew Phil grains or crystallized directly from stalled batches of kimberlitic magmas.Megacrysts,most macrocrysts and microcrysts are disintegrated phlogopite fragments from metasomatised peridotite and eclogite xenoliths.Fine phlogopite flakes within kimberlite groundmass represent mixing of high-Ti-Cr phlogopite antecrysts and high-Ti and low-Cr kimberlitic phlogopite with high Al and Ba contents that may have formed individual grains or overgrown antecrysts.Based on the results of this study,we propose a schematic model of SCLM metasomatism involving phlogopite crystallization,megacryst formation,and genesis of kimberlite magmas as recorded by the Grib pipe.     

大兴安岭北部诺敏河地幔金云母及钾质地幔熔体研究

在大兴安岭北部诺敏河第四纪钾质火山岩携带的地幔捕虏体中,发现少量金云母矿物和富钾地幔熔体。金云母颗粒大小1~5mm,呈网脉状充填在橄榄石和辉石、石榴子石等地幔矿物间隙。电子探针研究表明地幔橄榄石、单斜辉石、斜方辉石和石榴石等矿物几乎不含钾质成分(K2O0.01%),而金云母矿物成分具有高钾(K2O~10%)、高钛(Ti O25.41%~7.74%)的特点,暗示区域地幔钾的富集与金云母矿物有密切关系。地幔金云母的成因往往与富钾地幔流体/熔体的交代作用有关,在地幔捕虏体矿物反应边的硅酸盐熔体(囊体)中,发现富硅、富钾的熔体,K2O 4%~8%。结合前人地幔熔体研究,认为区域地幔经历了多期、不同成分地幔熔体的富集作用,其中富钾熔体对地幔钾质成分的富集起到重要作用。诺敏钾质火山正是富钾地幔部分熔融的产物,钾质熔体成分的来源可能与俯冲再循环的壳源物质有关。     

Evidence of diverse depletion and metasomatic events in harzburgite–lherzolite mantle xenoliths from the Iberian plate (Olot, NE Spain): Implications for lithosphere accretionary processes

Mantle xenoliths from the Olot volcanic district (NE Spain) comprise a bi-modal suite consisting of protogranular spinel lherzolites (cpx 12–14%) sometimes with pargasitic amphibole, and highly refractory spinel harzburgites (cpx ≤ 1%) with coarse-grained granular textures. The lherzolites range from slightly depleted to moderately LREE-enriched with flat HREE patterns between 1.5 and 2.7 × chondrite (Ch). In contrast, the harzburgites are extremely depleted in HREE (down to 0.2 × Ch) and strongly LREE-enriched (La_N/Yb_N = 12.3–17.2). LA-ICP-MS analyses of clinopyroxene and amphibole of the lherzolites highlight variable degrees of LREE depletion (HREE up to 13 × Ch, La_N/Yb_N down to 0.01), with the exception of a single sample in which both clinopyroxene and amphibole are LREE-enriched (La_N/Yb_N up to 19). In the harzburgites, clinopyroxenes display totally different REE distributions, characterized by extreme HREE depletion (down to 0.4 × Ch) and upward convex positively fractionated middle-light REE patterns (Nd_N/Yb_N up to 20.7 × Ch; La_N/Yb_N up to 12 × Ch). Sr–Nd–Hf isotopic data for both whole-rocks and cpx separates, coherently indicate depleted mantle (DM) compositions for the lherzolites (εSr = − 15 to − 26, εNd = + 9 to + 17, εHf = + 18 to + 68) and enriched mantle (EM) compositions for the harzburgites (εSr = − 10 to + 36, εNd = − 1 to − 6, εHf = + 3 to + 8). Modelling of the clinopyroxene REE data and isotopic systematics suggest that some lherzolites were affected by pre-Paleozoic (0.6–1 By) low-degree partial melting processes, while others probably reflect some extent of refertilization of the mantle protolith by metasomatizing melts similar to the Triassic rift-related tholeiites reported from several Pyrenean localities. The harzburgites represent extreme refractory residua, resulting from a complex depletion history due to multistage melt extraction as often observed in the cratonic mantle. The distinctive REE patterns and isotopic systematics of their clinopyroxenes suggest that the harzburgites were formed by the interaction of an ultra-depleted peridotite matrix with highly alkaline basic melts similar in composition to the Permo-Triassic alkaline lamprophyres which are widespread within the Iberian plate. Lherzolites possibly represent younger lithosphere (accreted asthenosphere?) up-lifted and juxtaposed to the older subcontinental lithospheric mantle (harzburgites) during the post-Variscan rifting of the Iberian margin. These two genetically different, but adjoining, mantle domains intimately mingled along the northern Iberian margin during the subsequent plate convergence processes, leading to the close association of harzburgites and lherzolites observed in the Olot mantle xenoliths and in some Pyrenean peridotite massifs.     

Thermal and petrological structure of the lithosphere beneath Hannuoba, Sino-Korean Craton, China: evidence from xenoliths

Deep-seated xenoliths entrained in the Hannuoba basalts of the northern Sino-Korean Craton include mafic and felsic granulites, mantle wall-rock from spinel– and garnet–spinel peridotite facies, and basaltic crystallisation products from the spinel-pyroxenite and garnet-pyroxenite stability fields. The mineral compositions of the xenoliths have been used to estimate temperatures and, where possible, pressures of equilibration, and to construct a geothermal framework to interpret the upper mantle and lower crustal rock-type sequences for the region. The xenolith-derived paleogeotherm is constrained in the depth interval of 45–65 km and like others from areas of young basalt magmatism, is elevated and strongly convex toward the temperature axis. Two-pyroxene granulites give the lowest temperatures and garnet pyroxenites the highest, while the spinel lherzolites fall between these two groups. The present-day Moho beneath the Hannuoba area is defined at 42 km by seismic data, and coincides with the deepest occurrence of granulite. Above this boundary, there is a lower crust–upper mantle transition zone about 10-km thick, in which spinel lherzolites and mafic granulites (with variable plagioclase contents) are intermixed. It is inferred that this underplating has resulted in a lowering of the original pre-Cenozoic Moho (then coinciding with the crust–mantle boundary, CMB) from about 30 km to its present-day position and was due to intrusions of basaltic magmas that displaced peridotite mantle wall-rock and equilibrated to mafic granulites. Trace element patterns of the diopsides (analysed by laser ablation-ICPMS) from the Cr-diopside series spinel lherzolites and associated layered xenoliths (spinel lherzolites and pyroxenites) indicate a fertile uppermost mantle with moderate depletion by low degrees of partial melting and little evidence of metasomatic activity. The similarity in major and trace element compositions of the minerals in both rock types suggests that the layered ultramafic xenoliths formed by mantle deformation processes (metamorphic segregation), rather than by melt veining or metasomatism.     

Genesis and evolution of the lithospheric mantle beneath the Buffalo Head Terrane, Alberta (Canada)

Mantle xenoliths and xenocrysts were retrieved from three of the 88–86 Ma Buffalo Hills kimberlites (K6, K11, K14) for a reconnaissance study of the subcontinental lithospheric mantle (SCLM) beneath the Buffalo Head Terrane (Alberta, Canada). The xenoliths include spinel lherzolites, one garnet spinel lherzolite, garnet harzburgites, one sheared garnet lherzolite and pyroxenites. Pyroxenitic and wehrlitic garnet xenocrysts are derived primarily from the shallow mantle and lherzolitic garnet xenocrysts from the deep mantle. Harzburgite with Ca-saturated garnets is concentrated in a layer between 135–165 km depth. Garnet xenocrysts define a model conductive paleogeotherm corresponding to a heat flow of 38–39 mW/m². The sheared garnet lherzolite lies on an inflection of this geotherm and may constrain the depth of the lithosphere–asthenosphere boundary (LAB) beneath this region to ca 180 km depth.

A loss of >20% partial melt is recorded by spinel lherzolites and up to 60% by the garnet harzburgites, which may be related to lithosphere formation. The mantle was subsequently modified during at least two metasomatic events. An older metasomatic event is evident in incompatible-element enrichments in homogeneous equilibrated garnet and clinopyroxene. Silicate melt metasomatism predominated in the deep lithosphere and led to enrichments in the HFSE with minor enrichments in LREE. Metasomatism by small-volume volatile-rich melts, such as carbonatite, appears to have been more important in the shallow lithosphere and led to enrichments in LREE with minor enrichments in HFSE. An intermediate metasomatic style, possibly a signature of volatile-rich silicate melts, is also recognised. These metasomatic styles may be related through modification of a single melt during progressive interaction with the mantle. This metasomatism is suggested to have occurred during Paleoproterozoic rifting of the Buffalo Head Terrane from the neighbouring Rae Province and may be responsible for the evolution of some samples toward unradiogenic Nd and Hf isotopic compositions.

Disturbed Re–Os isotope systematics, evident in implausible model ages, were obtained in situ for sulfides in several spinel lherzolites and suggest that many sulfides are secondary (metasomatic) or mixtures of primary and secondary sulfides. Sulfide in one peridotite has unradiogenic ¹⁸⁷Os/¹⁸⁸Os and gives a model age of 1.89±0.38 Ga. This age coincides with the inferred emplacement of mafic sheets in the crust and suggests that the melts parental to the intrusions interacted with the lithospheric mantle.

A younger metasomatic event is indicated by the occurrence of sulfide-rich melt patches, unequilibrated mineral compositions and overgrowths on spinel that are Ti-, Cr- and Fe-rich but Zn-poor. Subsequent cooling is recorded by fine exsolution lamellae in the pyroxenes and by arrested mineral reactions.

If the lithosphere beneath the Buffalo Head Terrane was formed in the Archaean, any unambiguous signatures of this ancient origin may have been obliterated during these multiple events.     

Triassic Nb-enriched basalts, magnesian andesites, and adakites of the Qiangtang terrane (Central Tibet): evidence for metasomatism by slab-derived melts in the mantle wedge

New chronological, geochemical, and isotopic data are reported for Triassic (219–236 Ma) adakite-magnesian andesite-Nb-enriched basaltic rock associations from the Tuotuohe area, central Qiangtang terrane. The adakites and magnesian andesites are characterized by high Sr/Y (25–45), La/Yb (14–42) and Na₂O/K₂O (12–49) ratios, high Al₂O₃ (15.34–18.28 wt%) and moderate to high Sr concentrations (220–498 ppm) and ε_ND (t) (+0.86 to +1.21) values. Low enrichments of Th, Rb relative to Nb, and subequal normalized Nb and La contents, and enrichments of light rare earth elements combine to distinguish a group of Nb-enriched basaltic rocks (NEBs). They have positive ε_ND (t) (+2.57 to +5.16) values. Positive correlations between Th, La and Nb and an absence of negative Nb anomalies on mantle normalized plots indicate the NEBs are products of a mantle source metasomatized by a slab melt rather than by hydrous fluids. A continuous compositional variation between adakites and magnesian andesites confirms slab melt interaction with mantle peridotite. The spatial association of the NEBs with adakites and magnesian andesites define an “adakitic metasomatic volcanic series” recognized in many demonstrably subduction-related environments (e.g., Mindanao arc, Philippines; Kamchatka arc, Russia; and southern Baja California arc, Mexico). The age of the Touhuohe suite, and its correlation with Triassic NEB to the north indicates that volcanism derived from subduction-modified mantle was abundant prior to 220 Ma in the central Qiangtang terrane.     

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.     

Os, Nd, and Sr isotopic and chemical compositions of ultramafic xenoliths from Kurose, SW Japan: Implications for contribution of slab-derived material to wedge mantle

We examined seven ultramafic xenoliths from 1~3 Ma alkali olivine basalt reefs near the Eurasian continent and one sample of the host alkali basalt to identify the mantle wedge material and to constrain the origin and evolution of mantle beneath SW Japan. Six xenoliths are from Kurose and one xenolith is from Takashima, northern part of the Kyushu islands, SW Japan. The Sr and Nd isotopic ratios vary from 0.70416 to 0.70773 and from 0.51228 to 0.51283, respectively. The Kurose and Takashima xenoliths have higher Sr isotopic ratios and lower Nd isotopic ratios than those of the peridotite xenoliths from the other arc settings such as Simcoe and NE Japan.

The Kurose xenoliths have less radiogenic Os isotopic ratios (¹⁸⁷Os/¹⁸⁸Os = 0.123–0.129) than the primitive upper mantle (PUM) estimate and limited variation compared to the other arc xenoliths. Their Os isotope compositions are rather similar to the ultramafic xenoliths from NE and east China. In addition, the samples of the Kurose and Takashima xenoliths plot along a mixing line between ultramafic xenoliths from SE and NE China and a slab component in Sr–Nd–Os isotopic space. Our results suggest that fragments of continental lithospheric mantle from the China craton may exist beneath Kurose and Takashima after the Sea of Japan expansion when the Japanese islands were rifted away from the Eurasian continent during Miocene. Later magmatism due to subduction of the Philippine Sea Plate beneath the SW Japan arc around 15 Ma ago may have introduced fluids or melts derived from slab component, interpreted to be oceanic sediments rather than altered oceanic crust, that possibly modified the original composition of the lithospheric mantle sampled by the peridotite xenoliths from Kurose and Takashima.     

中国大陆岩石圈地幔镍-钴-铂族元素组成及其成矿意义: 地幔捕虏体证据

镍、钴和铂族元素（PGEs,Platinum group elements）是我国紧缺的关键金属,它们作为亲铁元素主要储存在地核和地幔中。幔源岩浆作用能否超常富集镍、钴和铂族成矿在一定程度上取决于地幔源区这些元素的组成与富集程度,地幔捕虏体可揭示中国大陆岩石圈地幔镍、钴和铂族元素的组成与含量。本文总结了中国华北克拉通、华南克拉通和中亚造山带东部等主要构造单元地幔捕虏体中镍、钴和铂族元素的组成与含量,认为：（1）华北和华南克拉通岩石圈地幔镍、钴和铂族元素原始含量较高,高于原始地幔,且随深度增加而增加,是镍、钴和铂族元素成矿岩浆的有利地幔源区;（2）镍、钴和铂族元素以纳米原子团簇、合金或硫化物等形式赋存、运移与富集;（3）不同构造单元岩石圈地幔镍、钴和铂族元素的富集程度不同;（4）岩石圈地幔镍、钴和铂族元素含量从元古代到新生代有所降低,意味着该区存在镍、钴和铂族元素抽取的岩浆事件,故其成矿潜力巨大。

     

Depletion and enrichment processes in the lithospheric mantle beneath the Kola Peninsula (Russia): Evidence from spinel lherzolite and wehrlite xenoliths

A suite of spinel lherzolite and wehrlite xenoliths from a Devonian kimberlite dyke near Kandalaksha, Kola Peninsula, Russia, has been studied to determine the nature of the lithospheric mantle beneath the northern Baltic Shield. Olivine modal estimates and Fo content in the spinel lherzolite xenoliths reveal that the lithosphere beneath the Archaean–Proterozoic crust has some similarities to Phanerozoic lithospheric mantle elsewhere. Modal metasomatism is indicated by the presence of Ti-rich and Ti-poor phlogopite, pargasite, apatite and picroilmenite in the xenoliths. Wehrlite xenoliths are considered to represent localised high-pressure cumulates from mafic–ultramafic melts trapped within the mantle as veins or lenses. Equilibration temperatures range from 775 to 969 °C for the spinel lherzolite xenoliths and from 817 to 904 °C for the wehrlites.

Laser ablation ICP-MS data for incompatible trace elements in primary clinopyroxenes and metasomatic amphiboles from the spinel lherzolites show moderate levels of LREE enrichment. Replacement clinopyroxenes in the wehrlites are less enriched in LREE but richer in TiO₂. Fractional melt modelling for Y and Yb concentrations in clinopyroxenes from the spinel lherzolites indicates 7–8% partial melting of a primitive source. Such a volume of partial melt could be related to the 2.4–2.5 Ga intrusion of basaltic magmas (now metamorphosed to garnet granulites) in the lower crust of the northern Baltic Shield. The lithosphere beneath the Kola Peninsula has undergone several episodes of metasomatism. Both the spinel lherzolites and wehrlites were subjected to an incomplete carbonatitic metasomatic event, probably related to an early carbonatitic phase associated with the 360–380 Ma Devonian alkaline magmatism. This resulted in crystallisation of secondary clinopyroxene rims at the expense of primary orthopyroxenes, with development of secondary forsteritic olivine and apatite. Two separate metasomatic events resulted in the crystallisation of the Ti–Fe-rich amphibole, phlogopite and ilmenite in the wehrlites and the low Ti–Fe amphibole and phlogopite in the spinel lherzolites. Alternatively, a single metasomatic event with a chemically evolving melt may have produced the significant compositional differences seen in the amphibole and phlogopite between the spinel lherzolites and wehrlites. The calculated REE pattern of a melt in equilibrium with clinopyroxenes from a cpx-rich pocket is identical to that of the kimberlite host, indicating a close petrological relationship.     

Geochemical and isotopic characteristics and evolution of the Jurassic volcanic arc between Arica (18°30′S) and Tocopilla (22°S), North Chilean Coastal Cordillera

The present-day North Chilean Coastal Cordillera between 18°30′S and 22°S records an important part of the magmatic evolution of the Central Andes during the Jurassic. Calc-alkaline to subordinate tholeiitic members from four rock groups with biostratigraphically constrained age display incompatible element pattern characteristic of convergent plate-margin volcanism, whereas alkaline basalts of one group occurring in the Precordillera show OIB-type trace element signatures. The correlation of biostratigraphic ages, regional distribution, and composition of the volcanic rocks provides a basis for the discussion on geochemical evolution and isotope ratios.Major and trace element distributions of the volcanic rocks indicate their derivation from mantle-derived melts. LILE and LREE enrichments in calc-alkaline basaltic andesites to dacites and some of the tholeiites hint at the involvement of hydrous fluids during melting and mobile element transport processes. A part of the Early Bajocian to ?Lower Jurassic and Oxfordian andesites and dacites are adakite-like rocks with a substantial participation of slab melt and are characterized by high Sr/Y ratios and low HREE contents. The Middle Jurassic tholeiitic and calc-alkaline basalts and basaltic andesites have been transported and partly stored within a system of deep-seated feeder fissures and crustal strike-slip faults before eruption.The isotopic composition of Sr (⁸⁷Sr/⁸⁶Sr_i=0.7032-0.7056) and Nd (εNd_i=2.2-7.1) of the Jurassic volcanic rocks mostly fall in the range characteristic for mantle melts although some crustal components may have been involved. A few samples show slightly more radiogenic Sr isotopic composition, which is probably due to interaction with ancient sea-water. The Pb isotopic composition of the arc rocks is uncoupled from the isotopic composition of Sr and Nd and is dominated by the crustal component. Since the Cretaceous and Modern arc volcanic rocks show Pb isotopic compositions that can be largely explained by in situ Pb isotope growth of Jurassic arc volcanic rocks, we argue that the various Andean arc systems between 18°30′S and 22°S formed on the same type of basement.Most of the investigated samples have high Ba, Zr, and Th concentrations compared to island arc mafic volcanic rocks. About 20% of the Jurassic arc volcanics comprise of dacitic to rhyolitic rocks. These characteristics combined with the Pb isotopic composition that shows the influence of a Palaeozoic (or partly older) basement point to a continental margin setting for the North Chilean Jurassic arc. The distribution of the magmatic rocks throughout time, their textures, and the character of intercalated sedimentary rocks reflect westward movement of the magma sources and of the arc/back-arc boundary relative to the current coast line during the Early Bajocian on a broad front between 19°30′ and 21°S.     

Metasomatic reactions between carbonated plume melts and mantle harzburgite: the evidence from Friday and Domingo Seamounts (Juan Fernandez chain, SE Pacific)

Two submarine volcanoes (named Friday and Domingo) have been mapped and sampled to the west of the youngest island (Alexander Selkirk) in the Juan Fernandez chain, SE Pacific. Samples from the seamounts are fresh, highly vesicular olivine and plagioclase-phyric basanites. Their MgO contents lie between 7 and 4 wt.%. Major element variation trends, especially decreasing SiO₂ with increasing MgO, cannot be explained by crystal fractionation, and suggest the influence of CO₂ during partial melting. Highly incompatible element ratios in both Friday and Domingo magmas are identical, with the exception of ratios involving Th and Nb for which Domingo shows depletions. These depletions are coupled with depletions in Zr, Hf and Ca and enrichments in the heavy rare-earth elements and Al₂O₃. All these geochemical features can be explained if the Domingo magmas reacted with harzburgitic mantle materials during transit to the surface in a manner shown experimentally to occur during CO₂-dominated kimberlite magmatism. The metasomatism results in the stabilisation of clinopyroxene, rutile and zircon which withhold the elements depleted at Domingo, and the breakdown of garnet which releases HREE and Al into the magmas. Magmas erupting from the large, more mature Friday edifice have traversed a mantle region already metasomatised during earlier stages of volcanism and so are not significantly modified during passage. The Juan Fernandez trace element patterns are similar to the low ⁸⁷Sr/⁸⁶Sr, high ¹⁴³Nd/¹⁴⁴Nd components in many Pacific hotspots and to the pattern suggested for recycled, altered, dehydrated oceanic crust, implying that such recycled crust is a common component in many hotspots. Isotopically, the Juan Fernandez magmas lie between the composition of prevalent mantle (PREMA) and HIMU. Received: 11 November 1997 / Accepted: 9 November 1999     

Pyroxenite xenoliths and clinopyroxene megacrysts from the Cenozoic Jbel Saghro Volcanic Field (Anti-Atlas,Morocco): Petrography,mineral chemistry and equilibration conditions

A suite of mafic pyroxenite xenoliths and clinopyroxene megacrysts was brought to the surface by Cenozoic nephelinites of the Jbel Saghro Volcanic Field (Anti-Atlas, Morocco). The large population of samples was subdivided into five groups: (i) clinopyroxenites sensu stricto; (ii) olivine clinopyroxenites; (iii) mica-bearing clinopyroxenites; (iv) kaersutite-bearing clinopyroxenites; (v) clinopyroxene megacrysts. These xenoliths display a cumulate texture (adcumulate, heteradcumulate with poikilitic clinopyroxene including olivine). The clinopyroxenes have the composition of augite and show an appreciable variation of MgO (7.02–14.80 wt.%), TiO₂ (0.58–5.76 wt.%) and Al₂O₃ (2.81–12.38 wt.%) contents in grains. The clinopyroxenes are characterized by convex upward chondrite-normalized REE patterns, they display very similar trace element compositions with low contents of incompatible elements such as Rb (0−0.9 ppm), Ba (0.1–8.3 ppm), Th (0.1−0.3 ppm), U (0.01−0.04 ppm) and Nb (1.3–3.2 ppm). REE contents of the calculated melts in equilibrium with the clinopyroxene megacrysts and clinopyroxene from pyroxenite xenoliths are similar to those of the nephelinites exposed in Jbel Saghro. Crystallization temperatures of pyroxenite xenoliths and clinopyroxene megacrysts range from 950 °C to 1150 °C. Clinopyroxene barometry yielded pressure of crystallization ranging from 0.4 to 0.8 GPa for pyroxenite xenoliths and 0.3 to 0.7 GPa for clinopyroxene megacrysts. This pressure range is in agreement with pyroxenite xenoliths and clinopyroxene megacrysts being crystallized from their parental melts at the lower and upper crust.     

Laboratory measurement of P-wave velocity in crustal and upper mantle xenoliths from Ichino-megata, NE Japan: ultrabasic hydrous lower crust beneath the NE Honshu arc

Ultrasonic laboratory measurements of P-wave velocity (Vp) were carried out up to 1.0 GPa in a temperature range of 25–400 °C for crustal and mantle xenoliths of Ichino-megata, northeast Japan. The rocks used in the present study cover a nearly entire range of lithological variation of the Ichino-megata xenoliths and are considered as representative rock samples of the lower crust and upper mantle of the back arc side of the northeast (NE) Honshu arc. The Vp values measured at 25 °C and 1.0 GPa are 6.7–7.2 km/s for the hornblende gabbros (38.6–46.9 wt.% SiO₂), 7.2 km/s for the hornblende-pyroxene gabbro (43.8 wt.% SiO₂), 6.9–7.3 km/s for the amphibolites (36.1–44.3 wt.% SiO₂), 8.0–8.1 km/s for the spinel lherzolites (46.2–47.2 wt.% SiO₂) and 6.30 km/s for the biotite granite (72.1 wt.% SiO₂). Combining the present data with the Vp profile of the NE Honshu arc [Iwasaki, T., Kato, W., Moriya, T., Hasemi, A., Umino, N., Okada, T., Miyashita, K., Mizogami, T., Takeda, T., Sekine, S., Matsushima, T., Tashiro, K., Miyamachi, H. 2001. Extensional structure in northern Honshu Arc as inferred from seismic refraction/wide-angle reflection profiling. Geophys. Res. Lett. 28 (12), 2329–2332], we infer that the 15 km thick lower crust of the NE Honshu arc is composed of amphibolite and/or hornblende (±pyroxene) gabbro with ultrabasic composition. The present study suggests that the Vp range of the lower crustal layer (6.6–7.0 km/s) in the NE Honshu arc, which is significantly lower than that obtained from various seismic measurements (e.g. the northern Izu-Bonin-Mariana arc: 7.1–7.3 km/s), is due to the thick hydrous lower crustal layer where hornblende, plagioclase and magnetite are dominant.     

Volatile (S,Cl and F) and fluid mobile trace element compositions in melt inclusions: implications for variable fluid sources across the Kamchatka arc

Volatile element, major and trace element compositions were measured in glass inclusions in olivine from samples across the Kamchatka arc. Glasses were analyzed in reheated melt inclusions by electron microprobe for major elements, S and Cl, trace elements and F were determined by SIMS. Volatile element–trace element ratios correlated with fluid-mobile elements (B, Li) suggesting successive changes and three distinct fluid compositions with increasing slab depth. The Eastern Volcanic arc Front (EVF) was dominated by fluid highly enriched in B, Cl and chalcophile elements and also LILE (U, Th, Ba, Pb), F, S and LREE (La, Ce). This arc-front fluid contributed less to magmas from the central volcanic zone and was not involved in back arc magmatism. The Central Kamchatka Depression (CKD) was dominated by a second fluid enriched in S and U, showing the highest S/K₂O and U/Th ratios. Additionally this fluid was unusually enriched in ⁸⁷Sr and ¹⁸O. In the back arc Sredinny Ridge (SR) a third fluid was observed, highly enriched in F, Li, and Be as well as LILE and LREE. We argue from the decoupling of B and Li that dehydration of different water-rich minerals at different depths explains the presence of different fluids across the Kamchatka arc. In the arc front, fluids were derived from amphibole and serpentine dehydration and probably were water-rich, low in silica and high in B, LILE, sulfur and chlorine. Large amounts of water produced high degrees of melting below the EVF and CKD. Fluids below the CKD were released at a depth between 100 and 200 km due to dehydration of lawsonite and phengite and probably were poorer in water and richer in silica. Fluids released at high pressure conditions below the back arc (SR) probably were much denser and dissolved significant amounts of silicate minerals, and potentially carried high amounts of LILE and HFSE. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.