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1.
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 REEN 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.  相似文献   

2.
An extensive study of peridotitic sulfide inclusion bearing diamonds and their prospective harzburgitic host rocks from the 53 Ma Panda kimberlite pipe, Ekati Mine, NWT Canada, has been undertaken with the Re–Os system to establish their age and petrogenesis. Diamonds with peridotitic sulfide inclusions have poorly aggregated nitrogen (<30% N as B centers) at N contents of 200–800 ppm which differs from that of chromite and silicate bearing diamonds and indicates residence in the cooler portion of the Slave craton lithospheric mantle. For most of the sulfide inclusions, relatively low Re contents (average 0.457 ppm) and high Os contents (average 339 ppm) lead to extremely low 187Re/188Os, typically << 0.05. An age of 3.52 ± 0.17 Ga (MSWD = 0.46) and a precise initial 187Os/188Os of 0.1093 ± 0.0001 are given by a single regression of 11 inclusions from five diamonds that individually provide coincident internal isochrons. This initial Os isotopic composition is 6% enriched in 187Os over 3.5 Ga chondritic or primitive mantle. Sulfide inclusions with less radiogenic initial Os isotopic compositions reflect isotopic heterogeneity in diamond forming fluids. The harzburgites have even lower initial 187Os/188Os than the sulfide inclusions, some approaching the isotopic composition of 3.5 Ga chondritic mantle. In several cases isotopically distinct sulfides occur in different growth zones of the same diamond. This supports a model where C–O–H–S fluids carrying a radiogenic Os signature were introduced into depleted harzburgite and produced diamonds containing sulfides conforming to the 3.5 Ga isochron. Reaction of this fluid with harzburgite led to diamonds with less radiogenic inclusions while elevating the Os isotope ratios of some harzburgites. Subduction is a viable way of introducing such fluids. This implies a role for subduction in creating early continental nuclei at 3.5 Ga and generating peridotitic diamonds.Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.  相似文献   

3.
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.  相似文献   

4.
We analyzed mineral microinclusions in fibrous diamonds from the Wawa metaconglomerate (Superior craton) and Diavik kimberlites (Slave craton) and compared them with published compositions of large mineral inclusions in non-fibrous diamonds from these localities. The comparison, together with similar datasets available for Ekati and Koffiefontein kimberlites, suggest a general pattern of metasomatic alteration imposed on the ambient mantle by formation of fibrous diamond. Calcium and Fe enrichment of peridotitic garnet and pyroxenes and Fe enrichment of olivine associated with fibrous diamond-forming fluids contributes to refertilization of the cratonic mantle. Saline—carbonatitic—silicic fluid trapped by fibrous diamonds may represent one of the elusive agents of mantle refertilization. Calcium enrichment of peridotitic garnet and pyroxenes is expected in local mantle segments during fibrous diamond production, as Ca in the carbonatitic fluids is deposited into the surrounding mantle when oxidized carbon is reduced to diamond. Harzburgitic garnet evolves towards Ca-rich compositions even when it interacts with Ca-poor saline fluids. An unusual trend of Mg enrichment to Fo95–98 is observed in some olivine inclusions in Wawa fibrous diamonds. The trend may result from the carbonatitic composition of the fluid that promotes crystallization of magnesian olivine and preferentially oxidizes the fayalite component. We propose a generic model of fibrous and non-fibrous diamond formation from carbonatitic fluids that explains enrichment of the mantle in mafic magmaphile and incompatible elements and accounts for locally metasomatized compositions of diamond inclusions.  相似文献   

5.
To better understand the formative mechanism of the Cretaceous Gyeongsang Basin in South Korea, we determined the geochemical compositions of Early Cretaceous syntectonic basaltic rocks intercalated with basin sedimentary assemblages. Two distinct compositional groups appeared: tholeiitic to calc-alkaline basalts from the Yeongyang sub-basin and high-K to shoshonitic basaltic trachyandesites from the Jinju and Uiseong sub-basins. All collected samples exhibit patterns of light rare earth element enrichment and chondrite-normalized (La/Yb)N ratios ranging from 2.4 to 23.6. In a primitive-mantle-normalized spidergram, the samples show distinctive negative anomalies in Nb, Ta, and Ti and a positive anomaly in Pb. The basalts exhibit no or a weak positive U anomaly in a spidergram, but the basaltic trachyandesites show a negative U anomaly. The basalts have highly radiogenic Sr [(87Sr/86Sr)i = 0.70722–0.71145], slightly negative εNd, positive εHf [(εNd)i = −2.7 to 0.0; (εHf)i = +2.9 to +6.4], and radiogenic Pb isotopic compositions [(206Pb/204Pb)i = 18.20–19.19; (207Pb/204Pb)i = 15.60–15.77; (208Pb/204Pb)i = 38.38–39.11]. The basaltic trachyandesites are characterized by radiogenic Sr [(87Sr/86Sr)i = 0.70576–0.71119] and unradiogenic Nd, Hf, and Pb isotopic compositions [(εNd)i = −14.0 to −1.4; (εHf)i = −17.9 to +3.7; (206Pb/204Pb)i = 17.83–18.25; (207Pb/204Pb)i = 15.57–15.63; (208Pb/204Pb)i = 38.20–38.70]. The “crust-like” signatures, such as negative Nb–Ta anomalies, elevated Sr isotopic compositions, and negative εNd(t) and εHf(t) values, of the basaltic trachyandesites resemble the geochemistry of Early Cretaceous mafic volcanic rocks from the southern portion of the eastern North China Craton. Considering the lower-crust-like low U/Pb and high Th/U ratios and the unradiogenic Pb isotopic compositions, the basaltic trachyandesites are considered to be derived from lithospheric mantle modified by interaction with melts that originated from foundered eclogite. Basaltic volcanism in the Yeongyang sub-basin is coeval with the basaltic trachyandesite magmatism, but it exhibits an elevated 87Sr/86Sr ratio at a given 143Nd/144Nd and highly radiogenic Pb isotopic compositions, which imply an origin from an enriched but heterogeneous lithospheric mantle source. Melts from subducted altered oceanic basalt and pelagic sediments are considered to be the most likely source for the metasomatism. An extensional tectonic regime induced by highly oblique subduction of the Izanagi Plate beneath the eastern Asian margin during the Early Cretaceous might have triggered the opening of the Gyeongsang Basin. Lithospheric thinning and the resultant thermal effect of asthenospheric upwelling could have caused melting of the metasomatized lithospheric mantle, producing the Early Cretaceous basaltic volcanism in the Gyeongsang Basin.  相似文献   

6.
The Orapa and Jwaneng kimberlites are located along the western margin of the Kalahari Craton and the prevalence of eclogitic over peridotitic diamonds in both mines has recently been linked to lower P-wave velocities in the deep mantle lithosphere (relative to the bulk of the craton) to suggest a diamond formation event prompted by mid-Proterozoic growth and modification of preexisting Archean lithosphere (Shirey et al. 2002). Here we study peridotitic diamonds from both mines, with an emphasis on the style of metasomatic source enrichment, to evaluate their relationship with this major eclogitic diamond formation event. In their major element chemistry, the peridotitic inclusions compare well with a world-wide database but reveal differences to diamond sources located in the interior of the Western Terrane of the Kaapvaal block, where the classical mines in the Kimberley region are located. The most striking difference is the relative paucity of low-Ca (<2 wt% CaO in garnet) harzburgites and a low ratio of harzburgitic to lherzolitic garnets (2:1). This suggests that lithospheric mantle accreted to the rim of the Zimbabwe and Kaapvaal blocks was overall chemically less depleted. Alternatively, this more fertile signature may be assigned to stronger metasomatic re-enrichment but the trace element signature of garnet inclusions is not in favor of strong enrichment in major elements. For both mines the majority of lherzolitic and harzburgitic garnet inclusions are characterized by moderately sinusoidal REEN patterns and low Ti, Zr and Y contents, indicative of a metasomatic agent with very high LREE/HREE and low HFSE. This is consistent with metasomatism by a CHO-fluid or, as modeled by Burgess and Harte (2003), a highly fractionated, low-volume silicate melt from the MORB-source. In both cases, changes in the major element chemistry of the affected rocks will be limited. In a few garnets from Orapa preferential MREE enrichment is observed, suggesting that the percolating fluid/melt fractionated a LREE-phyllic phase (such as crichtonite). The overall moderate degree of metasomatism reflected by the inclusion chemistry is in stark contrast to lithospheric sections for Orapa and Jwaneng based on mantle xenocrysts and xenoliths, revealing extensive mantle metasomatism (Griffin et al. 2003). This suggests that the formation of peridotitic diamonds predates the intensive modification of the subcratonic lithosphere during Proterozoic rifting and compression, implying that diamonds may survive major tectonothermal events.Editorial responsibility: J. Hoefs  相似文献   

7.
Oxygen fugacity (fO2) conditions were determined for 29 peridotite xenoliths from the A154-North and A154-South kimberlites of the Diavik diamond mine using the newly developed flank method modified specifically for measuring Fe3+ in mantle-derived pyropic garnets. The results indicate that the garnet-bearing lithospheric mantle beneath the central Slave craton is vertically layered with respect to oxidation state. The shallow (<140 km), “ultra-depleted” layer is the most oxidized section of garnet-bearing subcratonic mantle thus far measured, up to one log unit more oxidizing relative to the FMQ buffer [Δlog fO2 (FMQ) + 1]. The lower, more fertile layer has fO2 conditions that extend down to Δlog fO2 (FMQ) − 3.8, consistent with xenolith suites from other localities worldwide. Based on trace element concentrations in garnets, two distinct metasomatic events affected the mantle lithosphere at Diavik. An oxidized fluid imparted sinusoidal chondrite-normalized REE patterns on garnets throughout the entire depth range sampled. In contrast, a reducing melt metasomatic event affected only the lower portion of the lithospheric mantle. The fO2 state of the Diavik mantle sample suggests that diamond formation occurred by reduction of carbonate by fluids arising from beneath the lithosphere.  相似文献   

8.
Trace element concentrations in the four principal peridotitic silicate phases (garnet, olivine, orthopyroxene, clinopyroxene) included in diamonds from Akwatia (Birim Field, Ghana) were determined using SIMS. Incompatible trace elements are hosted in garnet and clinopyroxene except for Sr which is equally distributed between orthopyroxene and garnet in harzburgitic paragenesis diamonds. The separation between lherzolitic and harzburgitic inclusion parageneses, which is commonly made using compositional fields for garnets in a CaO versus Cr2O3 diagram, is also apparent from the Ti and Sr contents in both olivine and garnet. Titanium is much higher in the lherzolitic and Sr in the harzburgitic inclusions. Chondrite normalised REE patterns of lherzolitic garnets are enriched (10–20 times chondrite) in HREE (LaN/YbN = 0.02–0.06) while harzburgitic garnets have sinusoidal REEN patterns, with the highest concentrations for Ce and Nd (2–8 times chondritic) and a minimum at Ho (0.2–0.7 times chondritic). Clinopyroxene inclusions show negative slopes with La enrichment 10–100 times chondritic and low Lu (0.1–1 times chondritic). Both a lherzolitic and a harzburgitic garnet with very high knorringite contents (14 and 21 wt% Cr2O3 respectively) could be readily distinguished from other garnets of their parageneses by much higher levels of LREE enrichment. The REE patterns for calculated melt compositions from lherzolitic garnet inclusions fall into the compositional field for kimberlitic-lamproitic and carbonatitic melts. Much more strongly fractionated REE patterns calculated from harzburgitic garnets, and low concentrations in Ti, Y, Zr, and Hf, differ significantly from known alkaline and carbonatitic melts and require a different agent. Equilibration temperatures for harzburgitic inclusions are generally below the C-H-O solidus of their paragenesis, those of lherzolitic inclusions are above. Crystallisation of harzburgitic diamonds from CO2-bearing melts or fluids may thus be excluded. Diamond inclusion chemistry and mineralogy also is inconsistent with known examples of metasomatism by H2O-rich melts. We therefore favour diamond precipitation by oxidation of CH4-rich fluids with highly fractionated trace element patterns which are possibly due to “chromatographic” fractionation processes. Received: 27 January 1996 / Accepted: 5 May 1997  相似文献   

9.
We have carried out a Pb double-spike and Lu-Hf isotope study of clinopyroxenes from spinel-facies mantle xenoliths entrained in Cenozoic intraplate continental volcanism of the French Massif Central (FMC). U-Th-Pb and Lu-Hf isotope systematics verify the existence of different lithospheric domains beneath the northern and southern FMC. Northern FMC clinopyroxenes have extreme Lu/Hf ratios and ultra-radiogenic Hf (εHf = +39.6 to +2586) that reflect ∼15-25% partial melting in Variscan times (depleted mantle model ages ∼360 Ma). Zr, Hf and Th abundances in these clinopyroxenes are low and unaffected by hydrous/carbonatitic metasomatism that overprinted LILE and light REE abundances and caused decoupling of Lu/Hf-Sm/Nd ratios and Nd-Hf isotopes (εNd = +2.1 to +91.2). Pb isotopes of northern FMC clinopyroxenes are radiogenic (206Pb/204Pb > 19), and typically more so than the host intraplate volcanic rocks. 238U/204Pb ratios range from 17 to 68, and most samples have distinctively low 232Th/238U (<1) and 232Th/204Pb (3-22). Clinopyroxenes from southern FMC lherzolites are generally marked by overall incompatible trace element enrichment including Zr, Hf and Th abundances, and have Pb isotopes that are similar to or less radiogenic than the host volcanic rocks. Hf isotope ratios are less radiogenic (εHf = +5.4 to +41.5) than northern FMC mantle and have been overprinted by silicate-melt-dominated metasomatism that affected this part of FMC mantle. Major element and Lu concentrations of clinopyroxenes from southern FMC harzburgites are broadly similar to northern FMC clinopyroxenes and suggest they experienced similar degrees of melt extraction as northern FMC mantle. 238U/204Pb (53-111) and 232Th/204Pb ratios (157-355) of enriched clinopyroxenes from the southern FMC are extreme and significantly higher than the intraplate volcanic rocks. In summary, mantle peridotites from different parts of the FMC record depletion at ∼360 Ma during Variscan subduction, followed by differing styles of enrichment. Northern FMC mantle was overprinted by a fluid/carbonatitic metasomatic agent that carried elements like U, Pb, Sr and light REE. In contrast, much of the southern FMC mantle was metasomatised by a small-degree partial silicate melt resulting in enrichment of all incompatible trace elements. The extreme mantle 238U/204Pb (northern and southern FMC), 232Th/238U (northern FMC) and 232Th/204Pb ratios (southern FMC), coupled with unremarkable present-day Pb isotope ratios, constrain the timing of enrichment. Mantle metasomatism is a young feature related to melting of the upwelling mantle responsible for Cenozoic FMC volcanism, rather than subduction-related metasomatism intimately associated with mantle depletion during the Variscan orogeny. The varying metasomatic styles relate to pre-existing variations in the thickness of the continental lithospheric lid, which controlled the extent to which upwelling mantle could ascend and melt. In the northern FMC, a thicker and more refractory lithospheric lid (?80 km) only allowed incipient degrees of melting resulting in fluid/carbonatitic metasomatism of the overlying sub-continental lithospheric mantle. The thinner lithospheric lid of the southern FMC (?70 km) allowed larger degrees of melting and resulted in silicate-melt-dominated metasomatism, and also focused the location of the volcanic fields of the FMC above this region.  相似文献   

10.
Although the diamond potential of cratons is linked mainly to thick and depleted Archean lithospheric keels, there are examples of craton-edge locations and circum-cratonic Proterozoic terranes underlain by diamondiferous mantle. Here, we use the results of comprehensive major and trace-element studies of detrital garnets from diamond-rich Late Triassic (Carnian) sedimentary rocks in the northeastern Siberia to constrain the thermal and chemical state of the pre-Triassic mantle and its ability to sustain the diamond storage. The studied detrital mantle-derived garnets are dominated by low- to medium-Cr lherzolitic (～45%) and low-Cr megacrystic (～39%) chemistries, with a significant proportion of eclogitic garnets (～11%), and only subordinate contribution from harzburgitic garnets (～5%) with variable Cr2O3 contents (1.2–8.4 wt.%). Low-Cr megacrysts display uniform, “normal” rare-earth element (REE) patterns with no Eu/Eu* anomalies, systematic Zr and Ti enrichment (mainly within 2.5–5), which are evidence of their crystallization from deep metasomatic melts. Lherzolitic (G9) garnets exhibit normal or humped to MREE-depleted sinusoidal REE patterns and elevated Nd/Y (up to 0.33–0.41) and Zr/Y ratios (up to 7.62). Rare low- to high-Cr harzburgitic (G10) garnets have primarily “depleted”, sinusoidal REE-patterns, low Ti, Y and HREE, but vary significantly in Zr-Hf, Ti and MREE-HREE contents, Nd/Y (within 0.1–2.4) and Zr/Y (1.53–19.9) ratios. The observed trends of chemical enrichment from the most depleted, harzburgitic garnets towards lherzolitic (including high-Ti high-Cr G11-type) garnets and megacrysts result from either voluminous high-temperature metasomatism by plume-derived silicate melts or recurrent mobilization of less voluminous kimberlitic or related carbonated mantle melts, rather than the initially primitive, fertile nature of the Proterozoic SCLM. Calculated Ni-in-garnet temperatures (primarily within ～1150–1250 °C) indicate their derivation from at least ～220 km thick Cr-undersaturated lithosphere at the relevant Devonian to Triassic thermal flow of ～45 mW/m2 or cooler. We suggest the existence of rare harzburgitic domains in the primarily lherzolitic diamond-facies SCLM beneath the northeastern Siberian craton at least by Triassic, whereas the abundance of eclogitic garnets, predominance of E-type inclusions in placer diamonds and specific morphologies argue for diamondiferous eclogites occurring within a ～50–65 kbar diamond window of the Olenek province by the same time.  相似文献   

11.
《Gondwana Research》2014,25(3-4):1152-1171
Many Cu–Mo–Au deposits are considered to be related to adakitic porphyries formed in non-arc settings, e.g., in collisional orogenic zones and intra-plate environments, but their genesis is still under discussion. The Aolunhua porphyry complex and its related Mo–Cu deposit from the eastern Central Asian Orogenic Belt (CAOB) provide important insights into this issue. The porphyries are characterized by high Sr (496–705 ppm) and Sr/Y and La/Yb ratios similar to those of typical adakitic rocks, and low ISr ratios (0.7049–0.7052) and positive εNd(t) (+ 0.5 to + 1.4) and εHf(t) (+ 3.5 to + 9.8) values. These features, along with the occurrence of mafic microgranular enclaves (MMEs), compositional and textural disequilibrium of plagioclase phenocrysts and relatively high Mg# values (45–52), indicate that they were derived from mixing of felsic magma from partial melting of a juvenile arc-type lower crust and mafic magma from a lithospheric mantle previously metasomatized by subduction zone fluids/melts. High Sr/Y and La/Yb ratios are indicative of contribution from enriched mantle-derived materials (with high LILEs; e.g., Sr, La), which were strengthened by subsequent fractionation of ferromagnesian phases such as pyroxene and hornblende. MMEs hosted by the ore-bearing porphyry have zircon U–Pb ages of ca. 132 Ma, similar to those of the host rocks. The enclaves have elevated Mg# (56–63), LILEs (e.g., Sr = 660–891 ppm), LREE (LaN = 68–150, (La/Sm)N = 3.0–4.0, (La/Yb)N = 12.0–19.6) and ratios of radiogenic isotopes of Nd- and Hf (εNd = + 0.7 to + 1.6; εHf = + 3.3 to + 10.9), suggesting that their parental magmas were derived from the metasomatized mantle source. The Mo–Cu mineralization was probably related to the high water content, high oxygen and sulfur fugacity of hybrid magma. Formation of the adakitic porphyries and related Mo–Cu deposits of the eastern CAOB could be related to the Early Cretaceous lithospheric extension, caused by the subduction of the Paleo-Pacific plate and its induced reactivation of juvenile arc-type lower crust.  相似文献   

12.
Peridotitic inclusions in alluvial diamonds from the Kankan region of Guinea in West Africa are mainly of lherzolitic paragenesis. Nevertheless, extreme Cr2O3 contents (max. 17 wt%) in some of the exclusively lherzolitic garnets document that the diamond source experienced a previous stage of melt extraction in the spinel stability field. This initial depletion was followed by at least two metasomatic stages: (1) enrichment of LREE and Sr and (2) introduction mainly of MREE–HREE and other HFSE (Ti, Y, Zr, Hf). The Ti- and HFSE-poor character of stage (1) points towards a CHO-rich fluid or carbonatitic melt, the high HFSE in stage (2) favour silicate melts as enriching agent. Eclogitic inclusions are derived from a large depth interval ranging from the lithosphere through the asthenosphere into the transition zone. The occurrence of negative Eu anomalies in garnet and clinopyroxene from both lithosphere and transition zone suggests a possible relationship to subducted oceanic crust. Lithospheric eclogitic inclusions are derived from heterogeneous sources, that may broadly be divided into a low-Ca group with LREE depleted trace element patterns and a high-Ca group representing a source with negative LREE–HREE slope that is moderately enriched in incompatible elements relative to primitive mantle. High-Ca inclusions of majoritic paragenesis are significantly more enriched in incompatible elements, such as in Sr and LREE. Calculated whole rock compositions require metasomatic enrichment even if a derivation from MORB is assumed. Received: 26 January 2000 / Accepted: 18 May 2000  相似文献   

13.
We have carried out a comparative Rb-Sr, Sm-Nd and Lu-Hf isotopic study of a progressively deformed hercynian leucogranite from the French Massif Central, belonging to the La Marche ductile shear zone, in order to investigate the respective perturbation of these geochronometers with fluid induced deformation. The one-meter wide outcrop presents a strongly deformed and mylonitized zone at the center, and an asymmetric deformation pattern with a higher deformation gradient on the northern side of the zone. Ten samples have been carefully collected every 10 cm North and South away from the strongest deformed mylonitic zone. They have been analyzed for a complete major, trace element data set, oxygen isotopes, Rb-Sr, Sm-Nd and Lu-Hf isotopic systematics.We show that most of major and trace elements except SiO2, alkaline elements (K2O, Rb), and some metal transition elements (Cu), are progressively depleted with increasing deformation. This depletion includes REE + Y, but also HFS elements (Ti, Hf, Zr, Nb) which are commonly considered as immobile elements during upper level processes. Variations in elemental ratios with deformation, e.g. decrease in LREE/MREE- HREE, Nd/Hf, Th/Sr, increase in Rb/Sr, U/Th and constant Sr/Nd, lead to propose the following order of element mobility: U ? Th > Sr = Nd ? Hf + HREE. We conclude in agreement with previous tectonic and metallogenic studies that trace element patterns across the shear zone result from circulation of oxidizing F-rich hydrothermal fluids associated with deformation. A temperature of the fluid of 470-480 °C can be deduced from the δ18O equilibrium between quartz-muscovite pairs.Elemental fractionation induces perturbation of the Rb-Sr geochronometer. The well-defined 87Rb/86Sr-87Sr/86Sr correlation gives an apparent age of 294 ± 19 Ma, slightly younger than the 323 ± 4 Ma age of leucogranites in this area. This apparent age is interpreted as dating event of intense deformation and fluid circulation associated with mass transfer, and exhumation of the ductile crust shortly after the leucogranite emplacement. Sm-Nd and Lu-Hf isochron-type diagrams do not define any correlation, because of the low fractionated Sm/Nd and Lu/Hf ratios. Isotopic data demonstrate that only the Lu-Hf geochronometer system is not affected by fluid circulation and gives reliable TDM age (1.29 ± 0.03 Ga) and εHf signatures. By contrast, the Sm-Nd geochronometer system gives erroneous old TDM ages of 2.84-4 Ga. There is no positive εNd-εHf correlation, because of decreasing εNd values with deformation at constant εHf values. However, εNd-εHf values remain in the broad εNd-εHf terrestrial array, which strongly indicates that fluid-induced fractionation can contribute to the width of the terrestrial array. The strong εHf negative values of the leucogranite are similar to metasedimentary granulitic xenoliths from the French Massif Central and confirm the generation of the leucogranite by several episodes of reworking of the lower crust.  相似文献   

14.
Oxidation of the Kaapvaal lithospheric mantle driven by metasomatism   总被引：2，自引：1，他引：1  
The oxidation state, reflected in the oxygen fugacity (fO2), of the subcratonic lithospheric mantle is laterally and vertically heterogeneous. In the garnet stability field, the Kaapvaal lithospheric mantle becomes progressively more reducing with increasing depth from Δlog fO2 FMQ-2 at 110 km to FMQ-4 at 210 km. Oxidation accompanying metasomatism has obscured this crystal-chemical controlled depth-fO2 trend in the mantle beneath Kimberley, South Africa. Chondrite normalized REE patterns for garnets, preserve evidence of a range in metasomatic enrichment from mild metasomatism in harzburgites to extensive metasomatism by LREE-enriched fluids and melts with fairly unfractionated LREE/HREE ratios in phlogopite-bearing lherzolites. The metasomatized xenoliths record redox conditions extending up to Δlog fO2 = FMQ, sufficiently oxidized that magnesite would be the stable host of carbon in the most metasomatized samples. The most oxidized lherzolites, those in or near the carbonate stability field, have the greatest modal abundance of phlogopite and clinopyroxene. Clinopyroxene is modally less abundant or absent in the most reduced peridotite samples. The infiltration of metasomatic fluids/melts into diamondiferous lithospheric mantle beneath the Kaapvaal craton converted reduced, anhydrous harzburgite into variably oxidized phlogopite-bearing lherzolite. Locally, portions of the lithospheric mantle were metasomatized and oxidized to an extent that conversion of diamond into carbonate should have occurred. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

15.
The Sr–Nd–Hf isotopic compositions of both saprolites and parent rocks of a profile of intensively weathered Neogene basalt in Hainan, South China are reported in this paper to investigate changes of isotopic systematics with high masses. The results indicate that all these isotopic systematics show significant changes in saprolites compared to those in corresponding parent rocks. The 87Sr/86Sr system was more seriously affected by weathering processes than other isotope systems, with εSr drifts 30 to 70 away from those of the parent rocks. In the upper profile (> 2.2 m), the Sr isotopes of the saprolites show an upward increasing trend with εSr changing from ~ 50 at 2.2 m to ~ 70 at 0.5 m, accompanying a upward increasing of Sr concentrations, from ~ 10 μg/g to ~ 25 μg/g. As nearly all the Sr of the parent rock has been removed during intensive weathering in this profile, the upward increasing of Sr concentrations in the upper profile suggests import of extraneous Sr. Rainwater in this region, which enriches in Sr (up to 139 μg/L) from seawater, may be the important extraneous source. Thus, the Sr isotopes of the saprolites in the upper profile may be mainly influenced by import of extraneous materials, and the Sr isotopic characteristics may not be retained. In contrast, the εNd and εHf of the saprolites drift only 0–2.6 and 0–3.7 away from the parent rocks, respectively. The negative drifts of the εNd and εHf are coupled with Nd and Hf losses in the saprolites; i.e., larger proportions of Nd and Hf loss correspond to lower εNd and εHf. Compared with the relative high Nd and Hf concentrations of the saprolites, the contributions of extraneous Nd and Hf both from wet and dry deposits of aeolian input are negligible. Thus, the εNd and εHf changes in the profile are mainly resulted from consecutive removal of the Nd and Hf. Calculation indicates that the 143Nd/144Nd and 176Hf/177Hf ratios in saprolites are all significantly lower than their initial values in the parent rock. Simply removing part of the Nd and Hf by incongruent decomposing some of the minerals may not account for this. Fractionation should be happen, which 143Nd and 176Hf may be preferentially removed from the profile relative to 144Nd and 177Hf during intensive chemical weathering, resulting in lower 143Nd/144Nd and 176Hf/177Hf ratios in saprolites relative to the parent rock, even though details for this process is not known. A positive correlation is observed between the εNd and εHf of the saprolites. Interestingly, the saprolites with a net loss of Nd and Hf in the upper profile show good positive correlation, and the regression line parallels the terrestrial array. By contrast, saprolites with a net gain of Nd and Hf in the lower profile generally show higher εHf values at a given εNd value, and the regression line between these εNd and εHf appears to parallel the seawater array. This supports the hypothesis that the contribution of continental Hf from chemical weathering release is the key to the obliquity of the seawater array away from the terrestrial array of the global εNd and εHf correlation. Our results also indicate that caution is needed when using εSr, εNd, and εHf to trace provenances for sediments and soils.  相似文献   

16.
The Baer ophiolitic massif is located in the northern sub-belt of the western segment of the Yarlung Zangbo Suture Zone (YZSZ) and mainly consists of a lherzolite-dominant mantle suite, dolerite intrusions and limited crustal outcrops. The dolerites show sub-ophitic texture and light rare earth element-depleted chondrite-normalized rare earth element patterns similar to normal-mid-ocean ridge basalts (N-MORB); though, they display enrichments in fluid-mobile elements (Rb, Ba, and Sr) and marked depletions in Th and Nb. The U–Pb ages of several magmatic zircon grains recovered from two dolerite samples indicate that the intrusion of the dikes into the Baer lherzolitic mantle occurred at 125.6–126.3 Ma, consistent with the widespread mafic magmatism between 120 and 130 Ma in the Yarlung Zangbo ophiolites. The dolerites have slightly more radiogenic 87Sr/86Sr ratios (0.7043–0.7054) in comparison to N-MORB, whereas they show 143Nd/144Nd values (0.513067–0.513114) similar to N-MORB and high zircon Hf-isotope compositions. They have a limited range of Nd-isotope (εNd(t) values: +8.2 to +9.1) and juvenile Hf-isotope compositions (εHf(t) values: +8.4 to +14.2 and +10.0 to +15.1) indicating derivation from mantle melts. The moderate spread in the εHf (t) values of zircons indicates derivation of the dolerites parental magma from a weakly contaminated spinel-bearing mantle source. This is also corroborated by the geochemical signatures of the Baer dolerites (enrichment in LILE and depletion in HFSE) suggesting minor slab input to the mantle source of the dike-filling melt. We suggest that the genesis of the dolerite dike-forming melt happened at a stage of subduction initiation in a sub-oceanic mantle domain mildly affected by fluids emanating from the downgoing slab. Our data combined with literature data allow us to presume that the intrusion of the dolerites into the Baer mantle corresponds to an early phase of subduction initiation beneath a developing forearc basin.  相似文献   

17.
87Sr/86Sr ratios of alkali olivine basalts, nepheline basanites and olivine nephelinites of Miocene age from the northern Hessian Depression vary between 0.7032 and 0.7036. Tholeiitic rocks from this area, which are possibly affected by crustal contamination, have more radiogenic Sr (0.7035 to 0.7042). Peridotite xenoliths with coarse protogranular (10 samples) and with porphyroclastic textures (2 samples) contain K- and Na-rich glasses which are products of reaction of metasomatic fluids with depleted peridotite. The Sr abundance in xenoliths is related to the amount of glass (and phlogopite).Sr ranges from 11 ppm to 147 ppm and 87Sr/86Sr ratios from 0.7033 to 0.7039. The isotopic ratios are neither correlated with Sr concentrations nor with Rb/Sr ratios. 87Sr/ 86Sr ratios of etched clinopyroxenes range from 0.7028 to 0.7040. In some xenoliths, clinopyroxenes differ from the whole rock samples significantly in their isotopic composition.If almost all of the pre-metasomatic Sr was located in the clinopyroxenes, the metasomatically introduced Sr ranges from 35 to 80% of the whole rock Sr. The calculated isotopic composition ranges from 0.7033 to 0.7040 for the majority of the xenoliths. For two pyroxenes which are not in isotopic equilibrium with the whole rock, the age of the metasomatic event could be estimated on the base of diffusion of Sr in clinopyroxene. Even assuming a diffusion coefficient as low as 10–15 cm2s–1 the time between the metasomatic alteration and the eruption of the basaltic host magma must be shorter than 1 Ma.The 87Sr/86Sr ratios of the basalts are interpreted as products of mixtures of a depleted component ( 0.7028) and metasomatic fluids (0.7035–0.7053) in their source peridotite.  相似文献   

18.
We report new Os-Pb-Hf isotope data for a suite of alkaline to basaltic (nephelinites, basanites, olivine tholeiites to quartz-tholeiites) lavas from the Miocene Vogelsberg (Germany), the largest of the rift-related continental volcanic complexes of the Central European Volcanic Province (CEVP). 187Os/188Os in primitive (high-MgO) alkaline lavas show a much wider range than has been observed in alkaline basalts and peridotite xenoliths from elsewhere in the CEVP, from ratios similar to those in modern MORB and OIB (0.1260-0.1451; 58.9-168 ppt Os) to more radiogenic ratios (0.1908 and 0.2197; 27.6-15.1 ppt Os). Radiogenic Os is associated with high εHf and εNd, low 87Sr/86Sr and does not correlate with Mg∗ or incompatible trace elements (e.g. Ce/Pb), suggesting the presence of a radiogenic endmember in the mantle rather than crustal contamination as the source of radiogenic Os. This contrasts with another high-Mg alkaline lava characterized by highly radiogenic 187Os/188Os (0.4344, 10.3 ppt Os), lower εHf and εNd, higher 87Sr/86Sr, and Pb isotope signatures than the other alkaline lavas with similar trace element composition suggestive of contamination with crustal material. Hafnium (εHf: +8.9 to +5.0) and Pb isotope compositions (206Pb/204Pb: 19.10-19.61; 207Pb/204Pb: 15.56-15.60) of the alkaline rocks fall within the range of enriched MORB and some OIB. The Vogelsberg tholeiites show even more diverse 187Os/188Os, ranging from 0.1487 in Os-rich olivine tholeiite (31.7 ppt) to ratios as high as 0.7526 in other olivine-tholeiites and in quartz-tholeiites with lower Os concentrations (10.3-2.0 ppt). Low-187Os/188Os tholeiites show Pb-Hf isotope ratios (206Pb/204Pb:18.81; 207Pb/204Pb: 15.61; εHf: +2.7) that are distinct from those in alkaline lavas with similar 187Os/188Os and originate from a different mantle source. By contrast, the combination of radiogenic Os and low 206Pb/204Pb and εHf in the other tholeiites probably reflects crustal contamination.The association at Vogelsberg of primitive alkaline and tholeiitic lavas with a range of MORB- to OIB-like Os-Pb-Hf-Nd-Sr isotopic characteristics requires at least two asthenospheric magma sources. This is consistent with trace element modelling which suggests that the alkaline and tholeiitic parent magmas represent mixtures of melts from garnet and spinel peridotite sources (both with amphibole), implying an origin of the magmas in the garnet peridotite-spinel peridotite transition zone, probably at the asthenosphere-lithosphere interface. We propose that uncontaminated Vogelsberg lavas originated in ‘metasomatized’ mantle, involving a 3-stage model: (1) early carbonatite metasomatism several 10-100 Ma before the melting event (2) deposition of low-degree asthenospheric melts from carbonated peridotite at the lithosphere-asthenosphere thermal boundary produces hydrous amphibole-bearing veins or patches, and (3) remobilization of this modified lithospheric mantle into other asthenospheric melts passing through the same area later. In keeping with ‘metasomatized’ mantle models for other continental basalt provinces, we envisage that stage (2) is short-lived (few Ma), thus producing a prominent lithospheric trace element signature without changing the asthenospheric isotopic signatures. Models of this type can explain the peculiar mix of lithospheric (prominent depletions of Rb and K) and asthenospheric (OIB-like high 187Os/188Os, 143Nd/144Nd and 176Hf/177Hf) signatures observed in the Vogelsberg and many other continental basalt suites.  相似文献   

19.
Garnets and clinopyroxenes, intergrown with diamonds in 37 diamondites (“bort”, “polycrystalline diamond aggregates”, “polycrystalline diamond”, “framesite”), presumably from southern Africa, were analyzed for trace element contents by LA-ICP-MS. The intimate diamond-silicate intergrowths suggest that both precipitated from the same fluids during the same crystallization events. In this study we distinguish 5 chemical garnet groups: “peridotitic” (P), intermediate (I) and 3 “eclogitic” groups (E1, E2 and E3). Chondrite-normalized trace element patterns for the garnet groups roughly correlate with major element abundances. Most of P garnets show complex, mildly sinusoidal REEN patterns with relatively flat HREEN-MREEN, a small hump at Sm-Nd and depleted LREEN, and have relatively high contents of Nb, Ta, U, and Th. The REEN abundance patterns of E garnets differ by showing a continuous increase from LREE to HREE and depletion in LREE and highly incompatible elements relative to the P garnets. Of all garnet groups, E3 garnets are the poorest in highly incompatible trace elements and in Mg. Model equilibrium fluids for P garnets suggest crystallization from magnesian carbonate-bearing fluids/melts, which were very rich in incompatible trace elements — similar to kimberlites. Hypothetical equilibrium melts for E1 and E2 garnets are also magnesian and poorer in LREE and highly incompatible elements relative to typical kimberlitic or carbonatitic melts. Fluids that crystallized the P and most of the E garnets have similar mg numbers indicating a peridotitic source for both. The differences in Cr and highly incompatible element contents can be the result of differences in fluid formation and/or evolution rather than different source rock. The positive correlation of Cr2O3 and mg with the abundances of highly incompatible elements in garnets indicate fluid-rock fractionation processes rather than igneous fractional crystallization processes being responsible for the evolution of the diamondite-forming fluids.  相似文献   

20.
Graphite-bearing peridotites, pyroxenites and eclogite xenoliths from the Kaapvaal craton of southern Africa and the Siberian craton, Russia, have been studied with the aim of: 1) better characterising the abundance and distribution of elemental carbon in the shallow continental lithospheric mantle; (2) determining the isotopic composition of the graphite; (3) testing for significant metastability of graphite in mantle rocks using mineral thermobarometry. Graphite crystals in peridotie, pyroxenite and eclogite xenoliths have X-ray diffraction patterns and Raman spectra characteristic of highly crystalline graphite of high-temperature origin and are interpreted to have crystallised within the mantle. Thermobarometry on the graphite-peridotite assemblages using a variety of element partitions and formulations yield estimated equilibration conditions that plot at lower temperatures and pressures than diamondiferous assemblages. Moreover, estimated pressures and temperatures for the graphite-peridotites fall almost exclusively within the experimentally determined graphite stability field and thus we find no evidence for substantial graphite metastability. The carbon isotopic composition of graphite in peridotites from this and other studies varies from δ13 CPDB = ? 12.3 to ? ?3.8%o with a mean of-6.7‰, σ=2.1 (n=22) and a mode between-7 and-6‰. This mean is within one standard deviation of the-4‰ mean displayed by diamonds from peridotite xenoliths, and is identical to that of diamonds containing peridotite-suite inclusions. The carbon isotope range of graphite and diamonds in peridotites is more restricted than that observed for either phase in eclogites or pyroxenites. The isotopic range displayed by peridotite-suite graphite and diamond encompasses the carbon isotope range observed in mid-ocean-ridge-basalt (MORB) glasses and ocean-island basalts (OIB). Similarity between the isotopic compositions of carbon associated with cratonic peridotites and the carbon (as CO2) in oceanic magmas (MORB/OIB) indicates that the source of the fluids that deposited carbon, as graphite or diamond, in catonic peridotites lies within the convecting mantle, below the lithosphere. Textural observations provide evidence that some of graphite in cratonic peridotites is of sub-solidus metasomatic origin, probably deposited from a cooling C-H-O fluid phase permeating the lithosphere along fractures. Macrocrystalline graphite of primary appearance has not been found in mantle xenoliths from kimberlitic or basaltic rocks erupted away from cratonic areas. Hence, graphite in mantle-derived xenoliths appears to be restricted to Archaean cratons and occurs exclusively in low-temperature, coarse peridotites thought to be characteristic of the lithospheric mantle. The tectonic association of graphite within the mantle is very similar to that of diamond. It is unlikely that this restricted occurrence is due solely to unique conditions of oxygen fugacity in the cratonic lithospheric mantle because some peridotite xenoliths from off-craton localities are as reduced as those from within cratons. Radiogenic isotope systematics of peridotite-suite diamond inclusions suggest that diamond crystallisation was not directly related to the melting events that formed lithospheric peridotites. However, some diamond (and graphite?) crystallisation in southern Africa occurred within the time span associated with the stabilisation of the lithospheric mantle (Pearson et al. 1993). The nature of the process causing localisation of carbon in cratonic mantle roots is not yet clearly understood.  相似文献   

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