Sulphide inclusions in diamonds from the Koffiefontein kimberlite, S Africa: constraints on diamond ages and mantle Re–Os systematics

Re–Os isotope compositions of syngenetic sulphide inclusions in both eclogite suite (E-type) and peridotite suite (P-type) parageneses in diamonds from the Koffiefontein mine, South Africa have been analysed using a technique capable of analysing single inclusion grains, or, in some cases multiple inclusions from the same diamonds. Sulphide inclusion Ni contents broadly correlate with Os abundances in that low-Ni (6.8–8.7% Ni), E-type sulphides have 4.7 to 189 ppb Os whereas the two high-Ni (25%), P-type sulphides have 5986 and 6097 ppb Os. Two P-type sulphides from the same diamond define the first mineral isochron obtained for a single diamond which has an age of 69±30 Ma with chondritic initial ¹⁸⁷Os/¹⁸⁸Os. This indicates that the sulphides, and hence the host diamond, crystallised close to the time of kimberlite emplacement (90 Ma), in the Mesozoic. This is supported by Pb isotopic measurements of a fragment from one of the sulphides, together with the absence of significant Type IaB nitrogen aggregation in the host diamond lattice. E-type sulphide inclusions have radiogenic Os isotopic compositions, ¹⁸⁷Os/¹⁸⁸Os 0.346 to 2.28, and Re–Os model ages from 1.1 to 2.9 Ga. They define an array on a Re–Os isochron diagram that may be interpreted as defining a single period of E-type sulphide growth at 1.05±0.12 Ga, with an elevated initial ¹⁸⁷Os/¹⁸⁸Os. Alternatively, two episodes of sulphide crystallisation, from a chondritic reservoir, may be invoked in the Archaean and in the Proterozoic. The results for both P- and E-type diamonds point to a spectrum of diamond crystallisation ages. High contents of both Re and Os, and the similarity of Re/Os ratios of sulphide inclusions in diamonds to whole rock eclogite and peridotite xenoliths indicate that small amounts of sulphides can dominate the mantle budget of both these elements during melting. Recent addition to the lithospheric mantle of high-Os material similar to that from which the P-type sulphides crystallised may explain the variable, sometimes young Os model ages seen in whole rock xenolith Re–Os data.     

The water content and hydrogen isotope composition of continental lithospheric mantle and mantle-derived mafic igneous rocks in eastern China

The water contents of minerals and whole-rock in mantle-derived xenoliths from eastern China exhibit large variations and are generally lower than those from other on- and off-craton lithotectonic units. Nevertheless, the water contents of mineral and whole-rock in Junan peridotite xenoliths, which sourced from the juvenile lithospheric mantle, are generally higher than those elsewhere in eastern China. This suggests that the initial water content of juvenile lithospheric mantle is not low. There is no obvious correlation between the water contents and Mg^# values of minerals in the mantle xenoliths and no occurrence of diffusion profile in pyroxene, suggesting no relationship between the low water content of mantle xenolith and the diffusion loss of water during xenolith ascent with host basaltic magmas. If the subcontinental lithospheric mantle (SCLM) base is heated by the asthenospheric mantle, the diffusion loss of water is expected to occur. On the other hand, extraction of basaltic melts from the SCLM is a more efficient mechanism to reduce the water content of xenoliths. The primary melts of Mesozoic and Cenozoic basalts in eastern China have water contents, as calculated from the water contents of phenocrysts, higher than those of normal mid-ocean ridge basalts (MORB). The Mesozoic basalts exhibit similar water contents to those of island arc basalts, whereas the Cenozoic basalts exhibit comparable water contents to oceanic island basalts and backarc basin basalts with some of them resembling island arc basalts. These observations suggest the water enrichment in the mantle source of continental basalts due to metasomatism by aqueous fluids and hydrous melts derived from dehydration and melting of deeply subducted crust. Mantle-derived megacrysts, minerals in xenoliths and phenocrysts in basalts from eastern China also exhibit largely variable hydrogen isotope compositions, indicating a large isotopic heterogeneity for the Cenozoic SCLM in eastern China. The water content that is higher than that of depleted MORB mantle and the hydrogen isotope composition that is deviated from that of depleted MORB mantle suggest that the Cenozoic continental lithospheric mantle suffered the metasomatism by hydrous melts derived from partial melting of the subducted Pacific slab below eastern China continent. The metasomatism would lead to the increase of water content in the SCLM base and then to the decrease of its viscosity. As a consequence, the SCLM base would be weakened and thus susceptible to tectonic erosion and delamination. As such, the crust-mantle interaction in oceanic subduction channel is the major cause for thinning of the craton lithosphere in North China.     

The longevity of subcontinental lithospheric mantle beneath Jiangsu-Anhui Region ——The Os isotope model age of mantle-derived peridotite xenoliths

The basalt-borne peridotite xenoliths from Jiangsu-Anhui provinces were analyzed for whole rock Os isotopic compositions in two laboratories of USTC, China and CRPG, France, respectively. The 187Os/188Os ratio of the sample set ranges from 0.119 to 0.129 (25 samples, USTC)and from 0.117 to 0.131 (17 samples, CRPG). The Os isotopic compositions of most samples are less than 0.129 and depleted relatively to the primitive mantle, showing a good correlation with the major element compositions. With the 187Os/188Os-Al2O3 alumichron, the samples yield a model age of 2.5 ± 0.1 Ga (data of USTC) and 1.9 ± 0.1 Ga (data of CRPG), late Archean to early Proterozoic, The two samples with the lowest 187Os/188Os ratio (0.119 and 0.117) have the TRD (Re depleted age) of 1.1 Ga (USTC) and 1.4 Ga (CRPG), mid-Proterozoic. The Os isotope model age shows that the peridotite xenoliths from Cenozoic alkali basalt in Jiangsu-Anhui provinces have an old formation age (early- to mid- Proterozoic). They are not newly produced mantle after the Phanerozoic replacement of the lithosphere mantle, but residual fractions of Proterozoic mantle.     

Ancient Os isotope signatures from the Ontong Java Plateau lithosphere: Tracing lithospheric accretion history

In order to better understand the nature and formation of oceanic lithosphere beneath the Early Cretaceous Ontong Java Plateau, Re–Os isotopes have been analysed in a suite of peridotite xenoliths from Malaita, Solomon Islands. Geological, thermobarometric and petrological evidence from previous studies reveal that the xenoliths represent virtually the entire thickness of the southern part of subplateau lithospheric mantle (< 120 km). This study demonstrates that vertical Os isotopic variations correlate with compositional variations in a stratified lithosphere. The shallowest plateau lithosphere (< 85 km) is dominated by fertile lherzolites showing a restricted range of ¹⁸⁷Os/¹⁸⁸Os (0.1222 to 0.1288), consistent with an origin from ~ 160 Ma Pacific lithosphere. In contrast, the basal section of subplateau lithospheric mantle (~ 95–120 km) is enriched in refractory harzburgites with highly unradiogenic ¹⁸⁷Os/¹⁸⁸Os ratios ranging from 0.1152 to 0.1196, which yield Proterozoic model ages of 0.9–1.7 Ga. Although the whole range of Os isotope compositions of Malaita peridotites is within the variations seen in modern abyssal peridotites, the contrasting isotopic compositions of shallow and deep plateau lithosphere suggest their derivation from different mantle reservoirs. We propose that the subplateau lithosphere forms a genetically unrelated two-layered structure, comprising shallower, typical oceanic lithosphere underpinned by deeper impinged material, which included a component of recycled Proterozoic lithosphere. The impingement of residual but chemically heterogeneous mantle, mechanically coupled to the recently formed, thin lithosphere, may have a bearing on the anomalous initial uplift and late subsidence history of the seismically anomalous plateau root.     

The longevity of subcontinental lithospheric mantle beneath Jiangsu-Anhui Region

The basalt-borne peridotite xenoliths from Jiangsu-Anhui provinces were analyzed for whole rock Os isotopic compositions in two laboratories of USTC, China and CRPG, France, respectively. The¹⁸⁷Os/¹⁸⁸Os ratio of the sample set ranges from 0.119 to 0.129 (25 samples, USTC) and from 0.117 to 0.131 (17 samples, CRPG). The Os isotopic compositions of most samples are less than 0.129 and depleted relatively to the primitive mantle, showing a good correlation with the major element compositions. With the¹⁸⁷Os/¹⁸⁸Os-Al₂O₃ alumichron, the samples yield a model age of 2.5 ± 0.1 Ga (data of USTC) and 1.9 ± 0.1 Ga (data of CRPG), late Archean to early Pro-terozoic. The two samples with the lowest¹⁸⁷Os/¹⁸⁸Os ratio (0.119 and 0.117) have the T_RD (Re depleted age) of 1.1 Ga (USTC) and 1.4 Ga (CRPG), mid-Proterozoic. The Os isotope model age shows that the peridotite xenoliths from Cenozoic alkali basalt in Jiangsu-Anhui provinces have an old formation age (early- to mid- Proterozoic). They are not newly produced mantle after the Phanerozoic replacement of the lithosphere mantle, but residual fractions of Proterozoic mantle.     

Characteristics of subcontinental lithospheric mantle beneath Baegryeong Island, Korea: Spinel peridotite xenoliths

Abstract   Geochemical data on Baegryeong Island spinel peridotites found in Miocene alkali basalt provide the information for lithosphere composition, chemical processes, equilibrium pressure and temperature conditions. Spinel peridotite xenoliths, showing transitional textures between protogranular and porpyroclastic textures, were accidentally trapped by the ascending alkali basalt magma. The xenoliths originate at depths from 50 to 70 km with a temperature range from 800 to 1100°C. The variations of modal and mineral compositions of the spinel peridotite xenoliths indicate that the xenoliths have undergone 1–10% fractional melting. The spinel peridotites from Baegryeong Island have undergone cryptic mantle metasomatism subsequent to melt extraction. Metasomatic agent of enriched spinel peridotite xenoliths was carbonatite melt.     

大陆岩石圈地幔形成与演化研究的新进展

研究大陆岩石圈地幔形成与演化的主要途径是利用岩石－地球化学探针研究幔源橄榄岩的年龄、组成及其演化，目前多将岩石圈地幔划分为大洋型和克拉通型，并认识到，岩石圈地幔的矿和相、成分、年龄在垂向上具有分层性；根据研究资料，目前已提出了以熔体抽取为岩石圈地幔形成的主要方式，并通过交代、拆沉等过程使岩石圈地幔遭受改造，中国东部岩石圈地幔的成分主体上是饱满的，与其上的太古代地壳并不协调，一些研究者提出了岩石圈拆沉和地幔置换两种具有代有性的模型来解释岩石圈地幔成分的这种特点，人们对中国东部岩石圈地幔作了大量的研究工作，然而，若要形成较为合理的解释，还需应用新技术（如，Re/Os同位素技术）做进一步的工作。     

Os–Hf–Sr–Nd isotope and PGE systematics of spinel peridotite xenoliths from Tok,SE Siberian craton: Effects of pervasive metasomatism in shallow refractory mantle

Os–Hf–Sr–Nd isotopes and PGE were determined in peridotite xenoliths carried to the surface by Quaternary alkali basaltic magmas in the Tokinsky Stanovik Range on the Aldan shield. These data constrain the timing and nature of partial melting and metasomatism in the lithospheric mantle beneath SE Siberian craton. The xenoliths range from the rare fertile spinel lherzolites to the more abundant, strongly metasomatised olivine-rich (70–84%) rocks. Hf–Sr–Nd isotope compositions of the xenoliths are mainly within the fields of oceanic basalts. Most metasomatised xenoliths have lower ¹⁴³Nd / ¹⁴⁴Nd and ¹⁷⁶Hf / ¹⁷⁷Hf and higher ⁸⁷Sr / ⁸⁶Sr than the host basalts indicating that the metasomatism is older and has distinct sources. A few xenoliths have elevated ¹⁷⁶Hf / ¹⁷⁷Hf (up to 0.2838) and plot above the Hf–Nd mantle array defined by oceanic basalts.¹⁸⁷Os / ¹⁸⁸Os in the poorly metasomatised, fertile to moderately refractory (Al₂O₃ ≥ 1.6%) Tok peridotites range from 0.1156 to 0.1282, with oldest rhenium depletion ages being about 2 Ga. The ¹⁸⁷Os / ¹⁸⁸Os in these rocks show good correlations with partial melting indices (e.g. Al₂O₃, modal cpx); the intercept of the Al–¹⁸⁷Os / ¹⁸⁸Os correlation with lowest Al₂O₃ estimates for melting residues (∼0.3–0.5%) has a ¹⁸⁷Os / ¹⁸⁸Os of ∼0.109 suggesting that these peridotites may have experienced melt extraction as early as 2.8 Gy ago. ¹⁸⁷Os / ¹⁸⁸Os in the strongly metasomatised, olivine-rich xenoliths (0.6–1.3% Al₂O₃) ranges from 0.1164 to 0.1275 and shows no apparent links to modal or chemical compositions. Convex-upward REE patterns and high abundances of heavy to middle REE in these refractory rocks indicate equilibration with evolved silicate melts at high melt / rock ratios, which may have also variably elevated their ¹⁸⁷Os / ¹⁸⁸Os. This inference is supported by enrichments in Pd and Pt on chondrite-normalised PGE abundance patterns in some of the rocks. The melt extraction ages for the Tok suite of 2.0 to 2.8 Ga are younger than oldest Os ages reported for central Siberian craton, but they must be considered minimum estimates because of the extensive metasomatism of the most refractory Tok peridotites. This metasomatism could have occurred in the late Mesozoic to early Cenozoic when the Tok region was close to the subduction-related Pacific margin of Siberia and experienced large-scale tectonic and magmatic activity. This study indicates that metasomatic effects on the Re–Os system in the shallow lithospheric mantle can be dramatic.     

Deep xenoliths in alkalic porphyry, Liuhe, Yunnan, and implications to petrogenesis of alkalic porphyry and associated mineralizations

Na-rich microlite-glass is first discovered in deep-source xenoliths in alkali-rich porphyry, Liuhe village, Heqing County, Yunnan Province. It is shown that the ultramafic xenoliths originated from partial melting of primary mantle and the glass resulted from metasomatism between the xenoliths and mantle fluid derived from mantle degassing. Mantle metasomatism not only resulted in the enrichment of alkaline, large-ion elements, ore metals and volatiles but also created a favorable condition for the generation of alkaline magmas. The mantle xenoliths and their characteristics of mantle metasomatism provide important evidence for a better understanding of the petrogenesis and mineralization of the Cenozoic alkali-rich porphyry in western Yunnan.     

Plume-lithosphere interactions in the ocean basins: constraints from the source mineralogy

Trace element relationships of near-primary alkalic lavas from La Grille volcano, Grande Comore, in the Indian Ocean, as well as those of the Honolulu volcanic series, Oahu, Hawaii, show that their sources contain amphibole and/or phlogopite. Small amounts of each mineral (2% amphibole in the source of La Grille and 0.5% phlogopite plus some amphibole in the source of the Honolulu volcanics) and a range of absolute degrees of partial melting from 1 to 5% for both series are consistent with the observed trace element variation. Amphibole and phlogopite are not stable at the temperatures of convecting upper mantle or upwelling thermal plumes from the deep mantle; however, they are stable at pressure-temperature conditions of the oceanic lithospheric mantle. Therefore, the presence of amphibole and/or phlogopite in the magma source region of volcanics is strong evidence for lithospheric melting, and we conclude that the La Grille and the Honolulu series formed by melting of the oceanic lithospheric mantle.

The identification of amphibole ± phlogopite in the source region of both series implies that the metasomatism by fluids or volatile-rich melts occurred prior to melting. The presence of hydrous phases results in a lower solidus temperature of the lithospheric mantle, which can be reached by conductive heating by the thermal plumes. Isotope ratios of the La Grille and the Honolulu series display a restricted range in composition and represent compositional end-members for each island. Larger isotopic variations in shield lavas, represented by the contemporaneous Karthala volcano on Grande Comore and the older Koolau series on Oahu, reflect interaction of the upwelling thermal plumes with the lithospheric mantle rather than the heterogeneity of deep-seated mantle plume sources or entrainment of mantle material in the rising plume. Literature OsSr isotope ratio covariations constrain the process of plume-lithosphere interaction as occurring through mixing of plume melts and low-degree melts from the metasomatized oceanic lithospheric mantle.

The characterization of the lithospheric mantle signature allows the isotopic composition of the deep mantle plume components to be identified, and mixing relationships show that the Karthala and Koolau plume end-members have nearly uniform isotopic compositions. Based on independent arguments, isotopic variations on Heard and Easter islands have been shown to be a result of mixing between deep plume sources having distinct isotopic compositions with lithosphere or shallow asthenospheric mantle. To the extent that these case studies are representative of oceanic island volcanism, they indicate that interaction with oceanic lithospheric mantle plays an important role in the compositions of lavas erupted during the shield-building stage of plume magmatism, and that isotopic compositions of deep mantle plume sources are nearly uniform on the scale that they are sampled by melting.     

Formation time of the big mantle wedge beneath eastern China and a new lithospheric thinning mechanism of the North China craton—Geodynamic effects of deep recycled carbon

High-resolution P wave tomography shows that the subducting Pacific slab is stagnant in the mantle transition zone and forms a big mantle wedge beneath eastern China. The Mg isotopic investigation of large numbers of mantle-derived volcanic rocks from eastern China has revealed that carbonates carried by the subducted slab have been recycled into the upper mantle and formed carbonated peridotite overlying the mantle transition zone, which becomes the sources of various basalts. These basalts display light Mg isotopic compositions(δ26 Mg = –0.60‰ to –0.30‰) and relatively low87 Sr/86 Sr ratios(0.70314–0.70564) with ages ranging from 106 Ma to Quaternary, suggesting that their mantle source had been hybridized by recycled magnesite with minor dolomite and their initial melting occurred at 300-360 km in depth. Therefore, the carbonate metasomatism of their mantle source should have occurred at the depth larger than 360 km, which means that the subducted slab should be stagnant in the mantle transition zone forming the big mantle wedge before 106 Ma. This timing supports the rollback model of subducting slab to form the big mantle wedge. Based on high P-T experiment results, when carbonated silicate melts produced by partial melting of carbonated peridotite was raising and reached the bottom(180–120 km in depth) of cratonic lithosphere in North China, the carbonated silicate melts should have 25–18 wt% CO2 contents, with lower Si O2 and Al2 O3 contents, and higher Ca O/Al2 O3 values, similar to those of nephelinites and basanites, and have higher εNdvalues(2 to 6). The carbonatited silicate melts migrated upward and metasomatized the overlying lithospheric mantle, resulting in carbonated peridotite in the bottom of continental lithosphere beneath eastern China. As the craton lithospheric geotherm intersects the solidus of carbonated peridotite at 130 km in depth, the carbonated peridotite in the bottom of cratonic lithosphere should be partially melted, thus its physical characters are similar to the asthenosphere and it could be easily replaced by convective mantle. The newly formed carbonated silicate melts will migrate upward and metasomatize the overlying lithospheric mantle. Similarly, such metasomatism and partial melting processes repeat, and as a result the cratonic lithosphere in North China would be thinning and the carbonated silicate partial melts will be transformed to high-Si O2 alkali basalts with lower εNdvalues(to-2). As the lithospheric thinning goes on,initial melting depth of carbonated peridotite must decrease from 130 km to close 70 km, because the craton geotherm changed to approach oceanic lithosphere geotherm along with lithospheric thinning of the North China craton. Consequently, the interaction between carbonated silicate melt and cratonic lithosphere is a possible mechanism for lithosphere thinning of the North China craton during the late Cretaceous and Cenozoic. Based on the age statistics of low δ26 Mg basalts in eastern China, the lithospheric thinning processes caused by carbonated metasomatism and partial melting in eastern China are limited in a timespan from 106 to25 Ma, but increased quickly after 25 Ma. Therefore, there are two peak times for the lithospheric thinning of the North China craton: the first peak in 135-115 Ma simultaneously with the cratonic destruction, and the second peak caused by interaction between carbonated silicate melt and lithosphere mainly after 25 Ma. The later decreased the lithospheric thickness to about70 km in the eastern part of North China craton.     

Effects of melt percolation on the Re-Os systematics of continental mantle lithosphere: A case study of spinel peridotite xenoliths from Heilongjiang,NE China

Os isotope ratios of mantle peridotites have been considered to be largely immune to recent melt-rock interaction. However, Os isotope ratios and PGE (Platinum group elements) concentrations of the Yong’an xenoliths have been significantly modified by melt percolation, and are not suitable for determining the formation age of lithosphere mantle in Yong’an. In this study, the Yong’an spinel peridotite xenoliths are divided into two groups: N-Type and E-Type. The N-Type group including cpx (clinopyroxene)-poor lherzolite and harzburgite, shows a large variation of Cr#(sp) (13.2-48) and sulfur contents (from 171 ppm to below detection limit), whereas the E-Type peridotites are mainly refractory harzburgites and are characterized by high Cr#(sp) (35.3-42.2) and overall low sulfur contents (below 51 ppm). Both types show similar major and REE (rare earth element) patterns. Furthermore, the N-Type peridotites display a restricted range of iridium-group PGE (IPGE), Os/Ir and Ru/Ir ratios (Os/Ir = 0.64-1.12, Ru/Ir = 1.52-1.79) and variable palladium-group PGE (PPGE) contents (3.4-14.9 ppb), whereas the E-Type peridotites show a large variation of Os/Ir and Ru/Ir ratios (Os/Ir = 0.33-0.84, Ru/Ir = 0.94-1.6), and a restricted range of PPGE (4.3-6.9 ppb). 187Os/188Os ratios of E-Type peridotites are higher than those of N-Type peridotites at comparable fertility levels. These results suggest that N-Type peridotites may have been overprinted by metasomatism via small melt fractions, in which the percolation of the volatile-rich, small melt fractions only resulted in LILE (large ion lithophile element) enrichment of clinopyroxene, and their whole rock PGE contents and Re-Os isotope values were little changed. Moreover, E-Type peridotites may have been modified by melt-rock reaction involving relatively large melt fractions, which may result in the formation of secondary cpx and olivine and the removal of IPGE-bearing minerals such as Ru-Os-(Ir) alloys or laurite, followed by precipitation of secondary sulfides from melt with radiogenic isotopic signature.     

Ultramafic xenoliths in mesozoic diorite in west shandong province

Deep-seated xenoliths are common in alkali ba-salts, kimberlites and lamprophyres[1]. These host rocks are all basic or ultrabasic volcanic and subvol-canic rocks originating from mantle. Reports of ul-tramafic xenoliths found in plutons are uncommon except those of Mesozoic diorites in North China[2—6]. This paper provides detailed mineralogy, petrology and geochemistry of ultramafic xenoliths in Tietong-gou pluton, Laiwu, Shandong Province, and discusses the possibility of their deep-sea…     

Lead,uranium, strontium,potassium and rubidium in inclusion-bearing diamonds and mantle-derived xenoliths from Southern Africa

Measurements are reported of K, Rb and Sr levels and Sr isotopic compositions in silicate inclusions in diamonds, and of U, Th and Pb levels and Pb isotopic compositions in sulphide inclusions in diamonds. Samples are from the Premier Mine (Transvaal), the Finsch Mine (northern Cape Province) and the Kimberley mines (northern Cape Province). The isotopic composition of Pb in sulphide inclusions indicates that the diamonds containing these inclusions are xenocrysts in the host kimberlite. Model Pb ages for the sulphide inclusions in the diamonds from Finsch and Kimberley are in excess of 2 b.y., although the host kimberlites are Cretaceous. The sulphide inclusions from Premier, however, have a model age similar to the emplacement age of the Premier kimberlites (approximately 1.2 b.y.).In addition, K, Rb, Sr, U and Pb concentrations and Sr and Pb isotopic compositions in clinopyroxenes from 14 mantle-derived xenoliths were measured. Samples were eclogites from the Roberts Victor Mine (Orange Free State), peridotites from the Matsoku Pipe (Lesotho) and diopside megacrysts from the four mines in Kimberley. The samples from the Roberts Victor Mine define a large spread in Sr and Pb isotopic composition. The slope of a regression line through the Pb data in the 207/204 vs. 206/204 plot defines an age of roughly 2.5 b.y. The Matsoku samples have⁸⁷Sr/⁸⁶Sr ratios around 0.704. One group of samples (“fertile peridotites”) shows uniform, anomalously radiogenic Pb isotopic compositions, and bears evidence of a young event involving isotopic homogenisation. Lead isotopic heterogeneity, indicating an old age, has persisted in another group (“common peridotites”). The megacrysts from the four Kimberley mines have⁸⁷Sr/⁸⁶Sr ratios around 0.704 and uniform, anomalously radiogenic Pb isotopic compositions, indicating a young age. Their Pb isotopic uniformity contrasts with the spread shown by kimberlites in Kimberley, and shows that the megacrysts did not crystallise in equilibrium with their host kimberlites.The similarity between the Pb isotopic data obtained on clinopyroxenes from xenoliths and the data obtained on sulphide inclusions in diamonds from Finsch and Kimberley suggests that these diamonds might be cogenetic with old rock provinces in the subcontinental mantle.     

Intracratonic asthenosphere upwelling and lithosphere rejuvenation beneath the Hoggar swell (Algeria): Evidence from HIMU metasomatised lherzolite mantle xenoliths

The mantle xenoliths included in Quaternary alkaline volcanics from the Manzaz-district (Central Hoggar) are proto-granular, anhydrous spinel lherzolites. Major and trace element analyses on bulk rocks and constituent mineral phases show that the primary compositions are widely overprinted by metasomatic processes. Trace element modelling of the metasomatised clinopyroxenes allows the inference that the metasomatic agents that enriched the lithospheric mantle were highly alkaline carbonate-rich melts such as nephelinites/melilitites (or as extreme silico-carbonatites). These metasomatic agents were characterized by a clear HIMU Sr–Nd–Pb isotopic signature, whereas there is no evidence of EM1 components recorded by the Hoggar Oligocene tholeiitic basalts. This can be interpreted as being due to replacement of the older cratonic lithospheric mantle, from which tholeiites generated, by asthenospheric upwelling dominated by the presence of an HIMU signature. Accordingly, this rejuvenated lithosphere (accreted asthenosphere without any EM influence), may represent an appropriate mantle section from which deep alkaline basic melts could have been generated and shallower mantle xenoliths sampled, respectively. The available data on lherzolite xenoliths and alkaline lavas (including He isotopes, Ra < 9) indicate that there is no requirement for a deep plume anchored in the lower mantle, and that sources in the upper mantle may satisfactorily account for all the geochemical/petrological/geophysical evidence that characterizes the Hoggar swell. Therefore the Hoggar volcanism, as well as other volcanic occurrences in the Saharan belt, are likely to be related to passive asthenospheric mantle uprising and decompression melting linked to tensional stresses in the lithosphere during Cenozoic reactivation and rifting of the Pan–African basement. This can be considered a far-field foreland reaction of the Africa–Europe collisional system since the Eocene.     

郯庐断裂带晚第三纪以来的浅部挤压活动与深部过程

郯庐断裂带晚第三纪以来持续遭受着挤压 ,使前期大规模的断陷盆地抬升、消亡 ,近代还是中国东部最大的地震活动带。断裂带所遭受的近WE向的挤压 ,是西太平洋弧后扩张和印度板块向北碰撞中的构造挤出作用产生的区域动力。断裂带在新生代挤压活动中切入上地幔 ,出现了地幔剪切、地幔交代、部分熔融等深部过程 ,最终形成了挤压背景下的陆内断裂带大规模的玄武岩喷发     

The Harrat Al-Birk basalts in southwest Saudi Arabia:characteristic alkali mafic magmatism related to Red Sea rifting

Harrat Al-Birk volcanics are products of the Red Sea rift in southwest Saudi Arabia that started in the Tertiary and reached its climax at ~ 5 Ma.This volcanic field is almost monotonous and is dominated by basalts that include mafic-ultramafic mantle xenoliths(gabbro,websterite,and garnet-clinopyroxenite).The present work presents the first detailed petrographic and geochemical notes about the basalts.They comprise vesicular basalt,porphyritic basalt,and flow-textured basalt,in addition to red and black scoria.Geochemically,the volcanic rock varieties of the Harrat Al-Birk are low- to medium-Ti,sodic-alkaline olivine basalts with an enriched oceanic island signature but extruded in a within-plate environment.There is evidence of formation by partial melting with a sort of crystal fractionation dominated by clinopyroxene and Fe-Ti oxides.The latter have abundant titanomagnetite and lesser ilmenite.There is a remarkable enrichment of light rare earth elements and depletion in Ba,Th and K,Ta,and Ti.The geochemical data in this work suggest Harrat Al-Birk basalts represent products of watersaturated melt that was silica undersaturated.This melt was brought to the surface through partial melting of asthenospheric upper mantle that produced enriched oceanic island basalts.Such partial melting is the result of subducted continental mantle lithosphere with considerable mantle metasomatism of subducted oceanic lithosphere that might contain hydrous phases in its peridotites.The fractional crystallization process was controlled by significant separation of clinopyroxene followed by amphiboles and Fe-Ti oxides,particularly ilmenite.Accordingly,the Harrat Al-Birk alkali basalts underwent crystal fractionation that is completely absent in the exotic mantle xenoliths(e.g.Nemeth et al.in The Pleistocene Jabal Akwa A1 Yamaniah maar/tuff ring-scoria cone complex as an analogy for future phreatomagmatic to magmatic explosive eruption scenarios in the Jizan Region,SW Saudi Arabia 2014).     

Platinum-group element micronuggets and refertilization process in Lherz orogenic peridotite (northeastern Pyrenees,France)

Highly siderophile elements (Platinum-group elements, Au and Re) are currently assumed to reside inside base metal sulfides (BMS) in the convecting upper mantle. However, fertile lherzolites sampled by Pyrenean orogenic peridotite massifs are unexpectedly rich in 0.5–3 µm large micronuggets of platinum-group minerals (PGM). Among those, sulfides from the laurite-erlichmanite series (Ru, Os(Ir)S(As)₂), Pt–Ir–Os alloys and Pt–Pd–Te–Bi phases (moncheite–merenskyite) are predominant. Not only the BMS phases but also the PGM micronuggets must be taken into account in calculation of the PGE budget of orogenic fertile lherzolites. Laurite is a good candidate for equilibrating the whole-rock budget of Os, Ir and Ru while accounting for supra-chondritic Ru/Ir_N. Textural relationships between PGMs and BMS highlight heterogeneous mixing between refractory PGMs (laurite/Pt–Ir–Os alloys) inherited from ancient refractory lithospheric mantle and late-magmatic metasomatic sulfides precipitated from tholeiitic melts. “Low-temperature” PGMs, especially Pt–Pd bismuthotellurides should be added to the list of mineral indicators of lithosphere refertilization process. Now disseminated within fertile lherzolites, “lithospheric“ PGMs likely account for local preservation of ancient Os model ages (up to 2 Ga) detected in BMS by in-situ isotopic analyses. These PGMs also question the reliability of orogenic lherzolites for estimating the PGE signature of the Primitive Silicate Earth.     

Deccan plume,lithosphere rifting,and volcanism in Kutch,India

Kutch (northwest India) experienced lithospheric thinning due to rifting and tholeiitic and alkalic volcanism related to the Deccan Traps K/T boundary event. Alkalic lavas, containing mantle xenoliths, form plug-like bodies that are aligned along broadly east–west rift faults. The mantle xenoliths are dominantly spinel wehrlite with fewer spinel lherzolite. Wehrlites are inferred to have formed by reaction between transient carbonatite melts and lherzolite forming the lithosphere. The alkalic lavas are primitive (Mg# = 64–72) relative to the tholeiites (Mg# = 38–54), and are enriched in incompatible trace elements. Isotope and trace element compositions of the tholeiites are similar to what are believed to be the crustally contaminated Deccan tholeiites from elsewhere in India. In terms of Hf, Nd, Sr, and Pb isotope ratios, all except two alkalic basalts plot in a tight cluster that largely overlap the Indian Ridge basalts and only slightly overlap the field of Reunion lavas. This suggests that the alkalic magmas came largely from the asthenosphere mixed with Reunion-like source that welled up beneath the rifted lithosphere. The two alkalic outliers have an affinity toward Group I kimberlites and may have come from an old enriched (metasomatized) asthenosphere. We present a new model for the metasomatism and rifting of the Kutch lithosphere, and magma generation from a CO₂-rich lherzolite mantle. In this model the earliest melts are carbonatite, which locally metasomatized the lithosphere. Further partial melting of CO₂-rich lherzolite at about 2–2.5 GPa from a mixed source of asthenosphere and Reunion-like plume material produced the alkalic melts. Such melts ascended along deep lithospheric rift faults, while devolatilizing and exploding their way up through the lithosphere. Tholeiites may have been generated from the main plume head further south of Kutch.     

Trace element and Sr and Nd isotope geochemistry of peridotite xenoliths from the Eifel (West Germany) and their bearing on the evolution of the subcontinental lithosphere

Peridotite xenoliths from the Eifel can be divided into incompatible element-depleted and -enriched members. The depleted group is restricted to dry lherzolites whereas the enriched group encompasses dry harzburgites, dry websterite and amphibole and/or phlogopite-bearing peridotites. Isotopically the depleted group is very diverse with¹⁴³Nd/¹⁴⁴Nd ranging from 0.51302 to 0.51355 and⁸⁷Sr/⁸⁶Sr from 0.7041 to 0.7019, thus occupying a field larger than expected for oceanic-type subcontinental mantle. These xenoliths are derived from a mantle which appears to have diverged from a bulk-earth Nd and Sr isotopic evolution path 2 Ga ago as a consequence of partial melting. The combination of high¹⁴³Nd/¹⁴⁴Nd with high⁸⁷Sr/⁸⁶Sr in some members of the depleted-xenoliths suite is likely to be the result of incipient reaction with incompatible element-enriched fluids in the mantle. In the enriched group such reactions have proceeded further and erased any pre-enrichment isotope memory resulting in a smaller isotopic diversity (¹⁴³Nd/¹⁴⁴Nd 0.51256–0.51273,⁸⁷Sr/⁸⁶Sr 0.7044–0.7032). An evaluation of SmHf and YbHf relationships suggests that the amphibole-bearing lherzolites and harzburgites acquired their high enrichment of light rare earth elements by fluid infiltration into previously depleted peridotite rather than by silicate melt-induced metasomatism. Upper mantle composed of such metasomatized peridotites does not represent a potential source for the basanites and nephelinites from the Eifel. The isotopic and chemical diversity of the subcontinental lithospheric part of the mantle may result from it having remained isolated from the convecting mantle for times > 1 Ga.