Mesozoic lithospheric mantle of the northeastern Siberian craton (evidence from inclusions in kimberlite)

Several thousand clinopyroxene, garnet, and phlogopite inclusions of mantle rocks from Jurassic and Triassic kimberlites in the northeastern Siberian craton have been analyzed and compared with their counterparts from Paleozoic kimberlites, including those rich in diamond. The new and published mineral chemistry data make a basis for an updated classification of kimberlite-hosted clinopyroxenes according to peridotitic and mafic (eclogite and pyroxenite) parageneses. The obtained results place constraints on the stability field of high-Na lherzolitic clinopyroxenes, which affect the coexisting garnet and decrease its Ca contents. As follows from analyses of the mantle minerals from Mesozoic kimberlites, the cratonic lithosphere contained more pyroxenite and eclogite in the Mesozoic than in the Paleozoic. It virtually lacked ultradepleted harzburgite-dunite lithologies and contained scarce eclogitic diamonds. On the other hand, both inclusions in diamond and individual eclogitic minerals from Mesozoic kimberlites differ from eclogitic inclusions in diamond from Triassic sediments in the northeastern Siberian craton. Xenocrystic phlogopites from the D’yanga pipe have ⁴⁰Ar/³⁹Ar ages of 384.6, 432.4, and 563.4 Ma, which record several stages of metasomatic impact on the lithosphere. These phlogopites are younger than most of Paleozoic phlogopites from the central part of the craton (Udachnaya kimberlite). Therefore, hydrous mantle metasomatism acted much later on the craton periphery than in the center. Monomineral clinopyroxene thermobarometry shows that Jurassic kimberlites from the northeastern craton part trapped lithospheric material from different maximum depths (170 km in the D’yanga pipe and mostly < 130 km in other pipes). The inferred thermal thickness of cratonic lithosphere decreased progressively from ~ 260 km in the Devonian-Carboniferous to ~ 225 km in the Triassic and to ~ 200 km in the Jurassic, while the heat flux (Hasterok-Chapman model) was 34.9, 36.7, and 39.0 mW/m², respectively. Dissimilar PT patterns of samples from closely spaced coeval kimberlites suggest different emplacement scenarios, which influenced both the PT variations across the lithosphere and the diamond potential of kimberlites.     

Aspects of diamond mineralisation and distribution at the Helam Mine, South Africa

The diamonds from the Swartruggens dyke swarm are mainly tetrahexahedra, with subsidiary octahedral and cuboid crystals. They are predominantly colourless, with subordinate yellows, browns, and greens. The existence of discrete cores and oscillatory growth structures within the diamonds, together with the recognition of harzburgite, lherzolite, at least two eclogitic and a websteritic diamond paragenesis, variable nitrogen contents, and both Type IaAB and Type Ib–IaA diamonds provides evidence for episodic diamond growth in at least six different environments. The predominance of plastic deformation in the diamonds, the state of nitrogen aggregation, and the suite of inclusion minerals recovered are all consistent with a xenocrystic origin for the diamonds, with the Type Ib–IaA diamonds being much younger than the rest. Mantle storage at a time-averaged temperature of ±1100 °C is inferred for the Type IaAB diamonds. The distribution of mantle xenocrysts of garnet and chromite within the high-grade Main kimberlite dyke compared to the low-grade Changehouse kimberlite dyke strongly suggests that the difference in diamond content is due to an increased eclogitic component of diamonds in the Main kimberlite dyke.     

Diamondiferous Archean rocks of the Olondo greenstone belt (western Aldan–Stanovoy shield)

Diamond from metaultramafic rocks of the Mesoarchean (2.96–3.0 Ga) Olondo greenstone belt, located in the western Aldan–Stanovoy shield, has been studied. Diamonds occur in lenses of olivine–serpentine–talc rocks within metaultramafic rocks of intrusive habit, whose composition corresponds to peridotite komatiites. All diamonds from the metaultramafic rocks are crystal fragments 0.3 to 0.5 mm in size. Morphological examination has revealed laminar octahedra, their transitional forms to dodecahedroids, crystals with polycentric faces, and spinel twins. The crystals vary in photoluminescence color: dark blue, green, yellow, red, or albescent. Characteristic absorption bands in crystals point to nitrogen impurities in the form of A and B1 defects and tabular B2 defects. The crystals studied belong to the IaA/B type, common among natural diamonds. The overall nitrogen content varies from < 100 to 3800 ppm. The relative content of nitrogen in B1 centers varies from 0 to 94%, pointing to long stay in the mantle. The carbon isotope ratio in the diamonds, ¹³C = ? 26‰, is indicative of involvement of subducted crust matter in diamond formation in the Archean.     

Archean diamonds from Wawa (Canada): samples from deep cratonic roots predating cratonization of the Superior Province

With an age of ca. 2.7 Ga, greenschist facies volcaniclastic rocks and lamprophyre dikes in the Wawa area (Superior Craton) host the only diamonds emplaced in the Archean available for study today. Nitrogen aggregation in Wawa diamonds ranges from Type IaA to IaB, suggesting mantle residence times of tens to hundreds of millions of years. The carbon isotopic composition (δ¹³C) of cube diamonds is similar to the accepted mantle value (− 5.0‰). Octahedral diamonds show a slight shift (by + 1.5‰) to isotopically less negative values suggesting a subduction-derived, isotopically heavy component in the diamond-forming fluids. Syngenetic inclusions in Wawa diamonds are exclusively peridotitic and, similar to many diamond occurrences worldwide, are dominated by the harzburgitic paragenesis. Compositionally they provide a perfect match to inclusions from diamonds with isotopically dated Paleo- to Mesoarchean crystallization ages. Several high-Cr harzburgitic garnet inclusions contain a small majorite component suggesting crystallization at depth of up to 300 km. Combining diamond and inclusion data indicates that Wawa diamonds formed and resided in a very thick package of chemically depleted lithospheric mantle that predates stabilization of the Superior Craton. If late granite blooms are interpreted as final stages of cratonization then a similar disconnect between Paleo- to Mesoarchean diamondiferous mantle lithosphere and Neoarchean cratonization is also apparent in other areas (e.g., the Lac de Gras area of the Slave Craton) and may suggest that early continental nuclei formed and retained their own diamondiferous roots.     

Rare and unusual mineral inclusions in diamonds from Mwadui, Tanzania

Syngenetic diamond inclusions from the Mwadui kimberlite reveal that an unusually fertile section of lithospheric mantle beneath the Central African Craton was sampled. This is shown by a very high ratio of lherzolitic to harzburgitic garnet inclusions (1:2) and low Mg/Fe-ratios in olivine and orthopyroxene. Geothermometry applied to the peridotitic inclusions indicates disequilibrium between non-touching inclusion pairs to be common. Disequilibrium between garnet-olivine and garnet-orthopyroxene pairs suggests successive iron enrichment during diamond formation, e.g. leading to the presence of harzburgitic garnet and lherzolitic olivine in the same diamond. Apart from the dominant peridotitic inclusion suite (88%), rare eclogitic inclusions occur (2%) and a number of uncertain paragenesis. Two diamonds, one with eclogitic garnets with moderate pyroxene solid solution and the other with a single ferro-periclase inclusion, suggest the contribution of a small sub-lithospheric component. The finding of the association Fe-FeO-Fe₃O₄ in one single diamond indicates diamond formation over a large range of f _O2 conditions, possibly along redox fronts. Steep compositional gradients may also be reflected by the joint occurrence of harzburgitic garnet and a SiO₂-phase in the same diamond. Alternatively the formation of the SiO₂-phase may be due to extreme carbonation of the peridotitic source. Further unusual findings include the exsolution of a silicate phase from magnetite inclusions, (i.e. primary solution of γ-olivine) and an ilmenite inclusion with an eskolaite (Cr₂O₃) component of 14.5 mol%, the latter together with harzburgitic paragenesis silicate inclusions. Received: 23 August 1997 / Accepted: 7 January 1998     

Major element composition of concentrate garnets in Proterozoic kimberlites from the Eastern Dharwar Craton,India: Implications on sub-continental lithospheric mantle

This study examines the major element composition of mantle-derived garnets recovered from heavy mineral concentrates of several Proterozoic kimberlites of the diamondiferous Wajrakarur Kimberlite Field (WKF) and the almost barren Narayanpet Kimberlite Field (NKF) in the Eastern Dharwar Craton of southern India. Concentrate garnets are abundant in the WKF kimberlites, and notably rare in the NKF kimberlites. Chemical characteristics of the pyropes indicate that the lithology of the sub-continental lithospheric mantle (SCLM) beneath both the kimberlite fields was mainly lherzolitic at the time of kimberlite eruption. A subset of green pyropes from the WKF is marked by high CaO and Cr₂O₃ contents, which imply contribution from a wehrlitic source. The lithological information on SCLM, when studied alongside geobarometry of lherzolite and harzburgite xenoliths, indicates that there are thin layers of harzburgite within a dominantly lherzolitic mantle in the depth interval of 115–190 km beneath the WKF. In addition, wehrlite and olivine clinopyroxenite occur locally in the depth range of 120–130 km. Mantle geotherm derived from xenoliths constrains the depth of graphite–diamond transition to 155 km beneath the kimberlite fields. Diamond in the WKF thus could have been derived from both lherzolitic and harzburgitic lithologies below this depth. The rarity of diamond and garnet xenocrysts in the NKF strongly suggest sampling of shallower (<155 km depth) mantle, and possibly a shallower source of kimberlite magma than at the WKF.     

Petrogenesis of the Late Cretaceous northern Alberta kimberlite province

At present, 48 Late Cretaceous (ca. 70–88 Ma) kimberlitic pipes have been discovered in three separate areas of the northern Alberta: the Mountain Lake cluster, the Buffalo Head Hills field and the Birch Mountains field. The regions can be distinguished from one another by their non-archetypal kimberlite signature (Mountain Lake) or, in the case of kimberlite fields, primitive (Buffalo Head Hills) to evolved (Birch Mountains) magmatic signatures.

The dominant process of magmatic differentiation is crystal fractionation and accumulation of olivine, which acts as the main criteria to distinguish between primitive and evolved Group I-type kimberlite fields in the northern Alberta. This is important from the viewpoint of diamond exploration because the majority (about 80%) of the more primitive Buffalo Head Hills kimberlites are diamondiferous, whereas the more evolved Birch Mountains pipes are barren of diamonds for the most part. Petrographically, the Buffalo Head Hills samples are distinct from the Birch Mountains samples in that they contain less carbonate, have a smaller modal abundance of late-stage minerals such as phlogopite and ilmenite, and have a higher amount of fresh, coarse macrocrystal (>0.5 mm) olivine. Consequently, samples from the Buffalo Head Hills have the highest values of MgO, Cr and Ni, and have chemistries similar to those of primitive hypabyssal kimberlite in the Northwest Territories. Based on whole-rock isotopic data, the Buffalo Head Hills K6 kimberlite has ⁸⁷Sr/⁸⁶Sr and _Nd values similar to those of South African Group I kimberlites, whereas the Birch Mountains Legend and Phoenix kimberlites have similar _Nd values (between 0 and +1.9), but distinctly higher ⁸⁷Sr/⁸⁶Sr values (0.7051–0.7063).

The lack of whole-rock geochemical overlap between kimberlite and the freshest, least contaminated Mountain Lake South pipe rocks reflects significant mineralogical differences and Mountain Lake is similar geochemically to olivine alkali basalt and/or basanite. Intra-field geochemical variations are also evident. The K4 pipe (Buffalo Head Hills), and Xena and Kendu pipes (Birch Mountains) are characterized by anomalous concentrations of incompatible elements relative to other northern Alberta kimberlite pipes, including chondrite-normalized rare-earth element distribution patterns that are less fractionated than the other kimberlite samples from the Buffalo Head Hills and Birch Mountains. The Xena pipe has similar major element chemical signatures and high-Al clinopyroxene similar to, or trending towards, the Mountain Lake pipes. In addition, K4 and Kendu have higher ⁸⁷Sr/⁸⁶Sr and lower _Nd than Bulk Earth and plot in the bottom right quadrant of the Nd–Sr diagram. We suggest, therefore, that the K4 and Kendu pipes contain a contribution from old, LREE-enriched (low Sm/Nd) lithosphere that is absent from the other kimberlites, are affected by crustal contamination, or both.

Based on xenocryst populations, the northern Alberta kimberlite province mantle is dominated by carbonate-saturated lherzolitic mantle. Higher levels of melt depletion characterize the Buffalo Head Hills mantle sample. Despite high diamondiferous to barren pipe ratios in the Buffalo Head Hills pipes, mineral indicators of high diamond potential, such as G10 garnet, diamond inclusion composition chrome spinels and high-sodium eclogitic garnet, are rare.     

Diamonds and their mineral inclusions from the A154 South pipe, Diavik Diamond Mine, Northwest territories, Canada

Mineral inclusions recovered from 100 diamonds from the A154 South kimberlite (Diavik Diamond Mines, Central Slave Craton, Canada) indicate largely peridotitic diamond sources (83%), with a minor (12%) eclogitic component. Inclusions of ferropericlase (4%) and diamond in diamond (1%) represent “undetermined” parageneses.

Compared to inclusions in diamonds from the Kaapvaal Craton, overall higher CaO contents (2.6 to 6.0 wt.%) of harzburgitic garnets and lower Mg-numbers (90.6 to 93.6) of olivines indicate diamond formation in a chemically less depleted environment. Peridotitic diamonds at A154 South formed in an exceptionally Zn-rich environment, with olivine inclusions containing more than twice the value (of  52 ppm) established for normal mantle olivine. Harzburgitic garnet inclusions generally have sinusoidal rare earth element (REE_N) patterns, enriched in LREE and depleted in HREE. A single analyzed lherzolitic garnet is re-enriched in middle to heavy REE resulting in a “normal” REE_N pattern. Two of the harzburgitic garnets have “transitional” REE_N patterns, broadly similar to that of the lherzolitic garnet. Eclogitic garnet inclusions have normal REE_N patterns similar to eclogitic garnets worldwide but at lower REE concentrations.

Carbon isotopic values (δ¹³C) range from − 10.5‰ to + 0.7‰, with 94% of diamonds falling between − 6.3‰ and − 4.0‰. Nitrogen concentrations range from below detection (< 10 ppm) to 3800 ppm and aggregation states cover the entire spectrum from poorly aggregated (Type IaA) to fully aggregated (Type IaB). Diamonds without evidence of previous plastic deformation (which may have accelerated nitrogen aggregation) typically have < 25% of their nitrogen in the fully aggregated B-centres. Assuming diamond formation beneath the Central Slave to have occurred in the Archean [Westerlund, K.J., Shirey, S.B., Richardson, S.H., Gurney, J.J., Harris, J.W., 2003b. Re–Os systematics of diamond inclusion sulfides from the Panda kimberlite, Slave craton. VIIIth International Kimberlite Conference, Victoria, Canada, Extended Abstracts, 5p.], such low aggregation states indicate mantle residence at fairly low temperatures (< 1100 °C). Geothermometry based on non-touching inclusion pairs, however, indicates diamond formation at temperatures around 1200 °C. To reconcile inclusion and nitrogen based temperature estimates, cooling by about 100–200 °C shortly after diamond formation is required.     

Origins of non-equilibrium lithium isotopic fractionation in xenolithic peridotite minerals: Examples from Tanzania

Olivine, clinopyroxene and orthopyroxene in variably metasomatised peridotite xenoliths from three lithospheric mantle sections beneath the East African Rift in Tanzania (Lashaine, Olmani, Labait) show systematic differences in their average Li concentrations (2.4 ppm, 2.0 ppm and 1.5 ppm, respectively) and intermineral isotopic fractionations, with olivine being heaviest (δ⁷Li = + 2.3 to + 13.9‰, average + 5.0‰), followed by orthopyroxene (? 4.1 to + 6.5‰, average + 0.8‰) and clinopyroxene (? 6.7 to + 4.1‰, average ? 1.6‰). These features are ascribed to the effects of kinetic Li isotope fractionation combined with different Li diffusivities in mantle minerals.Two main mechanisms likely generate diffusion-driven kinetic Li isotope fractionation in mantle xenoliths (1) Li diffusion from grain boundary melt into minerals during recent metasomatism or entrainment in the host magma and (2) subsolidus intermineral Li-redistribution. The latter can produce both isotopically light (Li-addition) and heavy (Li-loss) minerals and may occur in response to changes in pressure and/or temperature.Modelling shows that non-mantle-like δ⁷Li in clinopyroxene (< + 2‰), combined with apparent equilibrium olivine-clinopyroxene elemental partitioning in most peridotite xenoliths from all three Tanzanian localities probably reflects incipient Li addition during interaction with the host magma. Low δ⁷Li (< ? 3‰), combined with high Li concentrations (> 3 ppm) in some clinopyroxene may require very recent (minutes) Li ingress from a Li-rich melt (100s of ppm) having mantle-like δ⁷Li. This might happen during late fragmentation of some mantle xenoliths caused by a volatile- (and Li-) rich component exsolved from the host basalt. In contrast, high Li concentrations (> 2 ppm) and δ⁷Li (> 4‰) in olivine from many Labait and Olmani samples are attributed to an older, pre-entrainment enrichment event during which isotopic equilibrium was attained and whose signature was not corrupted during xenolith entrainment. Low Li concentrations and mantle-like isotopic composition of olivine from most Lashaine xenoliths indicate limited metasomatic Li addition.Thus, Li concentrations and isotope compositions of mantle peridotites worldwide may reflect two processes, with olivine mainly preserving a signature of depletion in refractory samples (low Li contents and δ⁷Li) or of older (precursory) melt addition in metasomatised samples (high Li contents and δ⁷Li), while non mantle-like, low δ⁷Li in almost all clinopyroxene can be due to Li ingress during transport in the host magma and/or slow cooling, if the samples were erupted in lavas. In Tanzania, the peridotites experienced rift-related heating prior to entrainment and were quenched upon eruption, so Li ingress is the most likely process responsible for the isotopically light clinopyroxene here.     

Re-Os isotopic composition of peridotitic sulphide inclusions in diamonds from Ellendale, Australia: Age constraints on Kimberley cratonic lithosphere

Sulphide-bearing diamonds recovered from the ∼20 Ma Ellendale 4 and 9 lamproite pipes in north-western Australia were investigated to determine the nitrogen aggregation state of the diamonds and Re-Os isotope geochemistry of the sulphide inclusions. The majority of diamond studies have been based on diamonds formed in the sub-continental lithospheric mantle (SCLM) below stable cratons, whereas the Ellendale lamproites intrude the King Leopold Orogen, south of the Kimberley craton. The sulphide inclusions consist of pyrrhotite-pentlandite-chalcopyrite assemblages, and can be divided into peridotitic and eclogitic parageneses on the basis of their Ni and Os contents. A lherzolitic paragenesis for the high-Ni sulphide inclusions is suggested from their Re and Os concentrations. Regression analysis of the Re-Os isotope data for the lherzolitic sulphides yields an age of 1426 ± 130 Ma, with an initial ¹⁸⁷Os/¹⁸⁸Os ratio of 0.1042 ± 0.0034. The upper limit of the uncertainty on the ¹⁸⁷Os/¹⁸⁸Os initial ratio gives a Re depletion age of 2.96 Ga, indicating the presence of SCLM beneath Ellendale since at least the Mesoarchaean, with the lherzolitic diamond-forming event much younger and unrelated to the craton keel stabilisation. The nitrogen aggregation state of the diamonds and calculated mantle residence temperatures suggest an origin and storage of the Ellendale diamonds in a stable cratonic SCLM, consistent with the King Leopold Orogen being cratonised by about 1.8 Ga. The diamonds do not show evidence for pervasive deformation or platelet degradation, which suggests that the diamonds had a relatively undisturbed 1.4 billion year mantle storage history.     

Oxygen isotope composition of syngenetic inclusions in diamond from the Finsch Mine,RSA

Oxygen isotope data have been obtained for silicate inclusions in diamonds, and similar associated minerals in peridotitic and eclogitic xenoliths from the Finsch kimberlite by laser-fluorination. Oxygen isotope analyses of syngenetic inclusions weighing 20–400 μg have been obtained by laser heating in the presence of ClF₃. ¹⁸O/¹⁶O ratios are determined on oxygen converted to CO₂ over hot graphite and, for samples weighing less than 750 μg (producing <12 μmoles O₂) enhanced CO production in the graphite reactor causes a systematic shift in both δ¹³C and δ¹⁸O that varies as a function of sample weight. A “pressure effect” correction procedure, based on the magnitude of δ¹³C (CO₂) depletion relative to δ¹³C (graphite), is used to obtain corrected δ¹⁸O values for inclusions with an accuracy estimated to be ±0.3‰ for samples weighing 40 μg.Syngenetic inclusions in host diamonds with similar δ¹³C values (−8.4‰ to −2.7‰) have oxygen isotope compositions that vary significantly, with a clear distinction between inclusions of peridotitic (+4.6‰ to +5.6‰) and eclogitic paragenesis (+5.7‰ to +8.0‰). The mean δ¹⁸O composition of olivine inclusions is indistinguishable from that of typical peridotitic mantle (5.25 ± 0.22‰) whereas syngenetic purple garnet inclusions possess relatively low δ¹⁸O values (5.00 ± 0.33‰). Reversed oxygen isotope fractionation between olivine and garnet in both diamond inclusions and diamondiferous peridotite xenoliths suggests that garnet preserves subtle isotopic disequilibrium related to genesis of Cr-rich garnet and/or exchange with the diamond-forming fluid. Garnet in eclogite xenoliths in kimberlite show a range of δ¹⁸O values from +2.3‰ to +7.3‰ but garnets in diamondiferous eclogites and as inclusions in diamond all have values >4.7‰.     

Inclusions in diamonds from the K14 and K10 kimberlites, Buffalo Hills, Alberta, Canada: diamond growth in a plume?

Analyses of mineral inclusions, carbon isotopes, nitrogen contents and nitrogen aggregation states in 29 diamonds from two Buffalo Hills kimberlites in northern Alberta, Canada were conducted. From 25 inclusion bearing diamonds, the following paragenetic abundances were found: peridotitic (48%), eclogitic (32%), eclogitic/websteritic (8%), websteritic (4%), ultradeep? (4%) and unknown (4%). Diamonds containing mineral inclusions of ferropericlase, and mixed eclogitic-asthenospheric-websteritic and eclogitic-websteritic mineral associations suggests the possibility of diamond growth over a range of depths and in a variety of mantle environments (lithosphere, asthenosphere and possibly lower mantle).

Eclogitic diamonds have a broad range of C-isotopic composition (δ¹³C=−21‰ to −5‰). Peridotitic, websteritic and ultradeep diamonds have typical mantle C-isotope values (δ¹³C=−4.9‰ av.), except for two ¹³C-depleted peridotitic (δ¹³C=−11.8‰, −14.6‰) and one ¹³C-depleted websteritic diamond (δ¹³C=−11.9‰). Infrared spectra from 29 diamonds identified two diamond groups: 75% are nitrogen-free (Type II) or have fully aggregated nitrogen defects (Type IaB) with platelet degradation and low to moderate nitrogen contents (av. 330 ppm-N); 25% have lower nitrogen aggregation states and higher nitrogen contents (30% IaB; <1600 ppm-N).

The combined evidence suggests two generations of diamond growth. Type II and Type IaB diamonds with ultradeep, peridotitic, eclogitic and websteritic inclusions crystallised from eclogitic and peridotitic rocks while moving in a dynamic environment from the asthenosphere and possibly the lower mantle to the base of the lithosphere. Mechanisms for diamond movement through the mantle could be by mantle convection, or an ascending plume. The interaction of partial melts with eclogitic and peridotitic lithologies may have produced the intermediate websteritic inclusion compositions, and can explain diamonds of mixed parageneses, and the overlap in C-isotope values between parageneses. Strong deformation and extremely high nitrogen aggregation states in some diamonds may indicate high mantle storage temperatures and strain in the diamond growth environment. A second diamond group, with Type IaA–IaB nitrogen aggregation and peridotitic inclusions, crystallised at the base of the cratonic lithosphere. All diamonds were subsequently sampled by kimberlites and transported to the Earth's surface.     

Mineral inclusions in diamonds from the Sputnik kimberlite pipe, Yakutia

The Sputnik kimberlite pipe is a small “satellite” of the larger Mir pipe in central Yakutia (Sakha), Russia. Study of 38 large diamonds (0.7-4.9 carats) showed that nine contain inclusions of the eclogitic paragenesis, while the remainder contain inclusions of the peridotitic paragenesis, or of uncertain paragenesis. The peridotitic inclusion suite comprises olivine, enstatite, Cr-diopside, chromite, Cr-pyrope garnet (both lherzolitic and harzburgitic), ilmenite, Ni-rich sulfide and a Ti-Cr-Fe-Mg-Sr-K phase of the lindsleyite-mathiasite (LIMA) series. The eclogitic inclusion suite comprises omphacite, garnet, Ni-poor sulfide, phlogopite and rutile. Peridotitic ilmenite inclusions have high Mg, Cr and Ni contents and high Nb/Zr ratios; they may be related to metasomatic ilmenites known from peridotite xenoliths in kimberlite. Eclogitic phlogopite is intergrown with omphacite, coexists with garnet, and has an unusually high TiO₂ content. Comparison with inclusions in diamonds from Mir shows general similarities, but differences in details of trace-element patterns. Large compositional variations among inclusions of one phase (olivine, garnet, chromite) within single diamonds indicate that the chemical environment of diamond crystallisation changed rapidly relative to diamond growth rates in many cases. P-T conditions of formation were calculated from multiphase inclusions and from trace element geothermobarometry of single inclusions. The geotherm at the time of diamond formation was near a 35 mW/m² conductive model; that is indistinguishable from the Paleozoic geotherm derived by studies of xenoliths and concentrate minerals from Mir. A range of Ni temperatures between garnet inclusions in single diamonds from both Mir and Sputnik suggests that many of the diamonds grew during thermal events affecting a relatively narrow depth range of the lithosphere, within the diamond stability field. The minor differences between inclusions in Mir and Sputnik may reflect lateral heterogeneity in the upper mantle.     

Diamonds from Jagersfontein (South Africa): messengers from the sublithospheric mantle

The diamond population from the Jagersfontein kimberlite is characterized by a high abundance of eclogitic, besides peridotitic and a small group of websteritic diamonds. The majority of inclusions indicate that the diamonds are formed in the subcratonic lithospheric mantle. Inclusions of the eclogitic paragenesis, which generally have a wide compositional range, include two groups of eclogitic garnets (high and low Ca) which are also distinct in their rare earth element composition. Within the eclogitic and websteritic suite, diamonds with inclusions of majoritic garnets were found, which provide evidence for their formation within the asthenosphere and transition zone. Unlike the lithospheric garnets all majoritic garnet inclusions show negative Eu-anomalies. A narrow range of isotopically light carbon compositions (δ¹³C −17 to −24 ‰) of the host diamonds suggests that diamond formation in the sublithospheric mantle is principally different to that in the lithosphere. Direct conversion from graphite in a subducting slab appears to be the main mechanism responsible for diamond formation in this part of the Earth’s mantle beneath the Kaapvaal Craton. The peridotitic inclusion suite at Jagersfontein is similar to other diamond deposits on the Kaapvaal Craton and characterized by harzburgitic to low-Ca harzburgitic compositions.     

Coupled lithium- and iron isotope fractionation during magmatic differentiation

In this study, we investigated Fe and Li isotope fractionation between mineral separates of olivine pheno- and xenocrysts (including one clinopyroxyene phenocryst) and their basaltic hosts. Samples were collected from the Canary Islands (Teneriffa, La Palma) and some German volcanic regions (Vogelsberg, Westerwald and Hegau). All investigated bulk samples fall in a tight range of Li and Fe isotope compositions (δ⁵⁶Fe_wr = 0.06–0.17‰ and δ⁷Li_ma = 2.5–5.2‰, assuming δ⁷Li of the olivine-free matrix is virtually identical to that of the bulk sample for mass balance reasons). In contrast, olivine phenocrysts display highly variable, but generally light Fe and mostly light Li isotope compositions compared to their respective olivine-free basaltic matrix, which was considered to represent the melt (with δ⁵⁶Fe_ol = ? 0.24 to 0.14‰ and δ⁷Li_ol = ? 10.5 to + 6.5‰, respectively). Single olivine crystals from one sample display even a larger range of δ⁵⁶Fe_ol between ? 0.7 and + 0.1‰. One single clinopyroxene phenocryst displays the lightest Li isotope composition (δ⁷Li_cpx = ? 17.7‰), but no Fe isotope fractionation relative to melt. The olivine phenocrysts show variable Mg# and Ni (correlated in most cases) that range between 0.89 and 0.74 and between 300 and 3000 μg/g, respectively. These olivines likely grew by fractional crystallization in an evolving magma. One sample from the Vogelsberg volcano contained olivine xenocrysts (Mg# > 0.89 and Ni > 3000 μg/g), in addition to olivine phenocrysts. This sample displays the highest Li- and the second highest Fe-isotope fractionation between olivine and melt (Δ⁷Li_ol-melt = ? 13; Δ⁵⁶Fe_ol-melt = ? 0.29).Our data, i.e. the variable olivine- at constant whole rock and matrix isotope compositions, strongly indicate disequilibrium, i.e. kinetic Fe and Li isotope fractionation between olivine and melt (for Li also between cpx and melt) during fractional crystallization. Δ⁷Li_ol-melt is correlated with the Li partitioning between olivine and melt (i.e. with Li_ol/Li_melt), indicating Li isotope fractionation due to preferential (faster) diffusion of ⁶Li into olivine during fractional crystallization. Olivine with low Δ⁷Li_ol-melt, also have low Δ⁵⁶Fe_ol-melt, indicating that Fe isotope fractionation is also driven by diffusion of isotopically light Fe into olivine, potentially, as Fe–Mg inter-diffusion. The lowest Δ⁵⁶Fe_ol-melt (? 0.40) was observed in a sample from Westerwald (Germany) with abundant magnetite, indicating relatively oxidizing conditions during magma differentiation. This may have enhanced equilibrium Fe isotope fractionation between olivine and melt or fine dispersed magnetite in the basalt matrix may have shifted its Fe isotope composition towards higher δ⁵⁶Fe. The decoupling of Li- and Fe isotope fractionation in cpx is likely due to faster diffusion of Li relative to Fe in cpx, implying that the large investigated cpx phenocryst resided in the magma for only a short period of time which was sufficient for Li- but not for Fe diffusion. The absence of any equilibrium Fe isotope fractionation between the investigated cpx phenocryst and its basaltic host may be related to the similar Fe^3 +/Fe^2 + of cpx and melt. In contrast to cpx, the generally light Fe isotope composition of all investigated olivine separates implies the existence of equilibrium- (in addition to diffusion-driven) isotope fractionation between olivine and melt, on the order of 0.1‰.     

Petrology and geochemistry of peridotite xenoliths from the Lianshan region: Nature and evolution of lithospheric mantle beneath the lower Yangtze block

Lithospheric thinning beneath the North China Craton is widely recognized, but whether the Yangtze block has undergone the same process is a controversial issue. Based on a detailed petrographic study, a suite of xenoliths from the Lianshan Cenozoic basalts have been analyzed for the compositions of minerals and whole rocks, and their Sr–Nd isotopes to probe the nature and evolution of the subcontinental lithospheric mantle beneath the lower Yangtze block. The Lianshan xenoliths can be subdivided into two Types: the main Type 1 xenoliths (9–15% clinopyroxene and olivine-Mg# < 90) and minor Type 2 peridotites (1.8–6.2% clinopyroxene and olivine-Mg# > 90). Type 1 peridotites are characterized by low MgO, high levels of basaltic components (i.e., Al₂O₃, CaO and TiO₂), LREE-depleted patterns in clinopyroxenes and whole rocks, and relatively high ¹⁴³Nd/¹⁴⁴Nd (0.513219–0.513331) and low ⁸⁶Sr/⁸⁷Sr (0.702279–0.702789). These features suggest that Type 1 peridotites represent fragments of the newly accreted fertile lithospheric mantle that have undergone ~ 1% of fractional partial melting and later weak silicate–melt metasomatism, similar to Phanerozoic lithospheric mantle beneath the eastern North China Craton. Type 2 peridotites may be shallow relics of the older lithospheric mantle depleted in basaltic components, with LREE-enriched and HREE-depleted patterns, relatively low ¹⁴³Nd/¹⁴⁴Nd (0.512499–0.512956) and high ⁸⁶Sr/⁸⁷Sr (0.703275–0.703997), which can be produced by 9–14% partial melting and subsequent carbonatite–melt metasomatism. Neither type shows a correlation between equilibration temperatures and Mg# in olivine, indicating that the lithospheric mantle is not compositionally stratified, but both types coexist at similar depths. This coexistence suggests that the residual refractory lithospheric mantle (i.e., Type 2 peridotites) may be irregularly eroded by upwelling asthenosphere materials along weak zones and eventually replaced to create a new and fertile lithosphere mantle (i.e., Type 1 xenoliths) as the asthenosphere cooled. Therefore, the subcontinental lithospheric mantle beneath the lower Yangtze block shared a common evolutional dynamic environment with that beneath the eastern North China Craton during late Mesozoic–Cenozoic time.     

Ultra-depleted peridotite xenoliths in the Northern Taihang Mountains: Implications for the nature of the lithospheric mantle beneath the North China Craton

We report the finding of peridotite xenoliths in the Early Cretaceous Longmengou olivine-bearing diabase (138 Ma) in the Northern Taihang Mountains in the central North China Craton. Based on the modal proportions of olivine, clinopyroxene, amphibole and anorthite, these peridotite xenoliths can be divided into three zones: clinopyroxene-bearing olivine zone (COZ), olivine-clinopyroxene zone (OCZ), and amphibole-bearing anorthite-clinopyroxene zone (AACZ). The core of olivine grains in clinopyroxene-bearing olivine zone have higher Mg^# (> 95), SiO₂ (41.80–42.53 wt%) and lower CaO (< 0.07 wt%), FeO (3.91–4.54 wt%) than the rim (Mg^# = 92.5–93.4, SiO₂ = 41.27–41.98 wt%, CaO = 0.20–0.34 wt%, and FeO = 7.02–8.87 wt%), suggesting that rim is reaction product. The core of olivine grains with higher Mg^# (> 95) and lower NiO content (< 0.04 wt%) in the clinopyroxene-bearing olivine zone was derived from ultra-depleted mantle subsequently altered by high Mg^# melts/magma with low Ni. Two generations of olivine grains occur in the OCZ where the first generation shows exsolution of ilmenite and magnetite rods containing up to 0.35 wt% TiO₂, and was likely derived from garnet peridotite hydrated by water. The second generation shows high Mg^# (96.2–97.1) and cataclastic texture, and was possibly formed by decomposition of the COZ. The occurrence of aluminous spinel suggests the role of melts with extremely high Al and Mg. Clinopyroxene in the AACZ shows systematic core-rim compositional variation with CaO and SiO₂ contents increasing towards the rim, and MgO and Fe₂O₃ concentrations decreasing from the core to the rim, indicating that the amphibole-bearing anorthite-clinopyroxene zone is a product of the reaction between mantle xenoliths and mafic magma. Plagioclase with high An value (92.0–99.95, average 97.79) indicates that the metasomatic melts have high Ca/Na and Al/Si ratios, possibly produced by the partial melting of ultra-depleted mantle under “wet” conditions. Combined with the data on other mantle xenoliths discovered in the NCC, our results suggest that the Mesozoic lithospheric mantle beneath the North Taihang Mountains within the central NCC is composed of ultra-depleted Archean and Paleoproterozoic peridotites and dunites modified by complex melts. We also propose that the destruction of eastern part of the NCC mainly occurred during Early Cretaceous, and that the boundary of the lithospheric destruction coincides with the Taihang Mountains.     

Water content in minerals of mantle xenoliths from the Udachnaya pipe kimberlites (Yakutia)

Distribution of water among the main rock-forming nominally anhydrous minerals of mantle xenoliths of peridotitic and eclogitic parageneses from the Udachnaya kimberlite pipe, Yakutia, has been studied by IR spectroscopy. The spectra of all minerals exhibit vibrations attributed to hydroxyl structural defects. The content of H₂O (ppm) in minerals of peridotites is as follows: 23–75 in olivine, 52–317 in orthopyroxene, 29–126 in clinopyroxene, and 0–95 in garnet. In eclogites, garnet contains up to 833 ppm H₂O, and clinopyroxene, up to 1898 ppm (~ 0.19 wt.%). The obtained data and the results of previous studies of minerals of mantle xenoliths show wide variations in H₂O contents both within different kimberlite provinces and within the Udachnaya kimberlite pipe. Judging from the volume ratios of mineral phases in the studied xenoliths, the water content varies over narrow ranges of values, 38–126 ppm. At the same time, the water content in the studied eclogite xenoliths is much higher and varies widely, 391–1112 ppm.     

Diamondiferous peridotitic microxenoliths from the Diavik Diamond Mine, NT

Twenty-five diamonds recovered from 21 diamondiferous peridotitic micro-xenoliths from the A154 South and North kimberlite pipes at Diavik (Slave Craton) match the general peridotitic diamond production at this mine with respect to colour, carbon isotopic composition, and nitrogen concentrations and aggregation states. Based on garnet compositions, the majority of the diamondiferous microxenoliths is lherzolitic (G9) in paragenesis, in stark contrast to a predominantly harzburgitic (G10) inclusion paragenesis for the general diamond production. For garnet inclusions in diamonds from A154 South, the lherzolitic paragenesis, compared to the harzburgitic paragenesis, is distinctly lower in Cr content. For microxenolith garnets, however, Cr contents for garnets of both the parageneses are similar and match those of the harzburgitic inclusion garnets. Assuming that the microxenolith diamonds reflect a sample of the general diamond population, the abundant Cr-rich lherzolitic garnets formed via metasomatic overprinting of original harzburgitic diamond sources subsequent to diamond formation, conversion of original harzburgitic diamond sources occurred in the course of metasomatic overprint re-fertilization. Metasomatic overprinting after diamond formation is supported by the finding of a highly magnesian olivine inclusion (Fo₉₅) in a microxenolith diamond that clearly formed in a much more depleted environment than indicated by the composition of its microxenolith host. Chondrite normalized REE patterns of microxenolith garnets are predominantly sinusoidal, similar to observations for inclusion garnets. Sinusoidal REE_N patterns are interpreted to indicate a relatively mild metasomatic overprint through a highly fractionated (very high LREE/HREE) fluid. The predominance of such patterns may explain why the proposed metasomatic conversion of harzburgite to lherzolite appears to have had no destructive effect on diamond content. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Geochemistry and Sr–Nd–Pb isotopic composition of the Harrat Al-Madinah Volcanic Field,Saudi Arabia

Whole-rock geochemical and Sr, Nd and Pb isotope data are presented for the Harrat Al-Madinah volcanic field, in the north western part of the Arabian plate, aiming to understand their origin and the composition of their mantle source. This area is an active volcanic field characterized by the occurrence of two historic eruptions approximately in 641 and 1256 A.D. Field investigation of the main volcanic landforms indicates dominantly monogenetic strombolian eruptions, in addition to local phreatomagmatic eruption style. The lavas consist mainly of alkali olivine basalt, olivine transitional basalt, and hawaiite with ocean island basalt (OIB)-like characteristics. Evolved rocks, represented by mugearites, benmoreites, and trachytes, occur mainly as domes, tuff cones and occasionally as lava flows. Chemical variations in the evolved rocks indicated their evolution by low pressure crystal fractionation of olivine, plagioclase, clinopyroxene, and Fe–Ti oxides from the relatively primitive basalts. The isotopic compositions of ¹⁴³Nd/¹⁴⁴Nd (0.512954–0.512995), ⁸⁷Sr/⁸⁶Sr (0.702899 to–0.702977) and Pb (²⁰⁶Pb/²⁰⁴Pb = 18.5515–18.7446, ²⁰⁷Pb/²⁰⁴Pb = 15.5120–15.5222, ²⁰⁸Pb/²⁰⁴Pb = 38.1347–38.4468), show restricted variations suggesting only minor crustal contamination. They defined an array consistent with mixing of two geochemically distinct components of depleted MORB-mantle (DMM) and high ²³⁸U/²⁰⁴Pb ratio (HIMU). The variations in Tb/Yb, La/Yb and Sm/Yb ratios in the relatively primitive basalts (MgO > 6 wt.%) indicated garnet peridotite source. However, the positive Nb, Sr, Ba and Ti anomalies in the primitive mantle-normalized incompatible element patterns and the significant variation between Zr/Nb vs. Ce/Y and La/Yb vs. Yb suggest contribution of an amphibole-bearing spinel lherzolite source. Moreover, the negative correlations between SiO₂ vs. ⁸⁷Sr/⁸⁶Sr and Th vs. ¹⁴³Nd/¹⁴⁴Nd are interpreted as an indication of mixing melts derived from two end-members; one is garnet bearing asthenospheric source with OIB characteristic and the other is amphibole-bearing spinel lherzolite. The Harrat Al-Madinah volcanic field occurs near the Red Sea Rift System and its origin reflects a strong lithospheric control on the loci of partial melting. The dominantly NNW alignment patterns of the volcanoes, which is similar to the regional Red Sea trend, may suggest that the magmas were produced by decompression partial melting triggered by lithospheric extension related to the Red Rift.