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1.
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.  相似文献   

2.
Rhenium (Re) is one of the least abundant elements in Earth, averaging 0.28 ppb in the primitive mantle. The unique occurrence of rheniite ReS2 (74.5 wt% of Re) in Kudryavy volcano precipitates raises questions about recycling of Re-rich reservoirs within the Kurile-Kamchatka volcanic Island arc setting. The sources of this unique Re enrichment have been inferred from studies of Re-Os isotope systematic and trace elements in volcanic gases, sulphide precipitates and host volcanic rocks. The fumarolic gas condensates are enriched in hydrophile trace elements relative to fluid-immobile elements and exhibit high Ba/Nb (133-204), Rb/Y (16-406) and Th/Zr (0.01-0.25) ratios. They are characterised by high Re (7-210 ppb) and Os abundances (0.4-0.9 ppb), with 187Os/188Os ratios in a range 0.122-0.152. This Os isotopic compositional range is similar to that of the peridotite xenoliths from the metasomatised mantle wedge above the subducted Pacific plate, the radiogenic isotopic signature of which is probably due to radiogenic addition from a slab-derived fluid.Re- and Os-rich sulphide and oxide minerals precipitate from volcanic gases within fumarolic fields. Molybdenite (MoS2), powellite (CaMoO4) and cannizzarite (Pb4Bi6S13) contain 1.5-1.7 wt%, 10 ppm, and 65-252 ppb of Re, respectively. Both molybdenite and rheniite contain normal Os concentrations, with total Os abundances in a range from 0.6 to 3.1 ppm for molybdenite, and 2.3-24.3 ppb for the rheniite samples. Repeated analyses of osmium isotope ratios for two rheniite samples form a best-fit line with an initial 187Os/188Os ratio of 0.32 ± 0.15 and an age of 79 ± 11 yr, which is the youngest age ever measured in natural samples. The high Re contents in molybdenite and rheniite led to high radiogenic 187Os values, even in the limited period of time, with 187Os/188Os ratios up to 3.3 for molybdenite and up to 4.4 for rheniite.The Os isotopic compositions of andesite-basaltic rocks from the Kudryavy volcano (187Os/188Os up to 0.326) are more radiogenic than those of residual peridotites and fumarolic gas condensates that are mainly constituted from magmatic vapor. Such radiogenic values can be attributed either to the addition of a radiogenic Os-rich subduction component to the depleted mantle, or to the assimilation of older dacitic caldera walls (187Os/188Os = 0.6) during arc magma ascent and emplacement. The latter hypothesis is supported by the correlation between 187Os/188Os ratio and indicators of fractionation such as MgO or Ni, and by low contents of potentially hydrophile trace elements such as Ba, Rb and Th relative to fluid-immobile elements such as Nb, Zr and Y. The high Re flux in the Kudryavy volcano (estimated at ∼46 kg/yr) can be explained by remobilisation of Re by Cl-rich water from an underplated mantle wedge and subducted organic-rich sediments of the Pacific plate.  相似文献   

3.
Highly siderophile element concentrations (HSE: Re and platinum-group elements (PGE)) are presented for gabbros, gabbroic eclogites and basaltic eclogites from the high-pressure Zermatt-Saas ophiolite terrain, Switzerland. Rhenium and PGE (Os, Ir, Ru, Rh, Pt, Pd) abundances in gabbro- and eclogite-hosted sulphides, and Re-Os isotopes and elemental concentrations in silicate phases are also reported. This work, therefore, provides whole rock and mineral-scale insights into the PGE budget of gabbroic oceanic crust and the effects of subduction metamorphism on gabbroic and basaltic crust.Chondrite-normalised PGE patterns for the gabbros are similar to published mid-ocean ridge basalts (MORB), but show less inter-element fractionation. Mean Pt and Pd contents of 360 and 530 pg/g, respectively, are broadly comparable to MORB, but gabbros have somewhat higher abundances of Os, Ir and Ru (mean: 64, 57 and 108 pg/g). Transformation to eclogite has not significantly changed the concentrations of the PGE, except Pd which is severely depleted in gabbroic eclogites relative to gabbros (∼75% loss). In contrast, basaltic eclogites display significant depletion of Pt (?60%), Pd (>85%) and Re (50-60%) compared with published MORB, while Os, Ir and Ru abundances are broadly comparable. Thus, these data suggest that only Pt, Pd and Re, and not Os, Ir and Ru, may be significantly fluxed into the mantle wedge from mafic oceanic crust. Re-Os model ages for gabbroic and gabbroic eclogite minerals are close to age estimates for igneous crystallisation and high-pressure metamorphism, respectively, hence the HSE budgets can be related to both igneous and metamorphic behaviour. The gabbroic budget of Os, Ir, Ru and Pd (but not Pt) is dominated by sulphide, which typically hosts >90% of the Os, whereas silicates account for most of the Re (with up to 75% in plagioclase alone). Sulphides in gabbroic eclogites tend to host a smaller proportion of the total Os (10-90%) while silicates are important hosts, probably reflecting Os inheritance from precursor phases. Garnet contains very high Re concentrations and may account for >50% of Re in some samples. The depletion of Pd in gabbroic eclogites appears linked, at least in part, to the loss of Ni-rich sulphide.Both basaltic and gabbroic oceanic crust have elevated Pt/Os ratios, but Pt/Re ratios are not sufficiently high to generate the coupled 186Os-187Os enrichments observed in some mantle melts, even without Pt loss from basaltic crust. However, the apparent mobility of Pt and Re in slab fluids provides an alternative mechanism for the generation of Pt- and Re-rich mantle material, recently proposed as a potential source of 187Os-186Os enrichment.  相似文献   

4.
The Yushui Cu-polymetallic deposit, which is associated with Ag, Pb, and Zn, is located in the middle part of the Yongan–Meixian Late Paleozoic Hercynian depression. It was discovered in eastern Guangdong Province in the late 1980s and is one of the richest copper deposits in China with high-grade copper averaging 3.25% and locally reaching 50–60%. The main ore body is located along the unconformity between the Upper Carboniferous Hutian Group limestone and the Lower Carboniferous Zhongxin Formation quartz sandstone with a bedded and lenticular morphology. The ores exhibit massive textures dominated by chalcopyrite, bornite, chalcocite, pyrite, sphalerite, galena, and a trace amount of argentite. Although researchers began studying the Yushui deposit in the early 1990s, the ore genesis remains controversial because of the lack of precise mineralisation age constraints. In this study, direct Re–Os dating of Cu sulphides aided in facilitating a better understanding of the timing of formation of the Yushui deposit. This study is the first attempt to use the Re–Os isotopic system for directly dating chalcopyrite and bornite ores for the Yushui deposit. The contents of Re, common Os, 187Re and 187Os in nine sulphides are 1.68–219.35 ppb, 0.003–0.427 ppb, 1.05–137.31 ppb, and 0.045–0.734 ppb, respectively. The isotope data yielded an isochron age of 308 ± 15 Ma (mean square weighted deviates = 2.4) using the 87Re/188Os–187Os/188Os plot, which is interpreted to represent the age of formation for these sulphides, suggesting that the mineralisation age of the Yushui deposit is close to the age of the host rocks. The 187Os/188Os initial value obtained from the Re–Os isochron is 1.81 ± 0.34, which corresponds to the γOs value of + 1349. This value indicates that the ore-forming materials were derived from the crust without mixing with materials from the mantle, and that the Yushui massive sulphide deposit may be of sedimentary exhalative origin.  相似文献   

5.
Analyses of enriched mantle (EM)-basalts, using lithophile element-based isotope systems, have long provided evidence for discrete mantle reservoirs with variable composition. Upon partial melting, the mantle reservoir imparts its isotopic fingerprint upon the partial melt produced. However, it has increasingly been recognised that it may not be simple to delimit these previously well-defined mantle reservoirs; the “mantle zoo” may contain more reservoirs than previously envisaged.Here we demonstrate that a simple model with varying contributions from two populations of compositionally distinct mantle sulphides can readily account for the observed heterogeneities in Os isotope systematics of such basalts without additional mantle reservoirs. Osmium elemental and isotopic analyses of individual sulphide grains separated from spinel lherzolites from Kilbourne Hole, New Mexico, USA demonstrate that two discrete populations of mantle sulphide exist in terms of both Re-Os systematics and textural relationship with co-existing silicates. One population, with a rounded morphology, is preserved in silicate grains and typically possesses high [Os] and low [Re] with unradiogenic, typically sub-chondritic 187Os/188Os attributable to long term isolation in a low-Re environment. By contrast, irregular-shaped sulphides, preserved along silicate grain boundaries, possess low [Os], higher [Re] and a wider range of, but generally supra-chondritic 187Os/188Os ([Os] typically ? 1-2 ppm, 187Os/188Os ? 0.3729; this study). This population is thought to represent metasomatic sulphide.Uncontaminated silicate phases contain negligible Os (<100 ppt) therefore the Os elemental and isotope composition of basalts is dominated by volumetrically insignificant sulphide ([Os] ? 37 ppm; this study). During the early stages of partial melting, supra-chondritic interstitial sulphides are mobilised and incorporated into the melt, adding their radiogenic 187Os/188Os signature. Only when sulphides armoured within silicates are exposed to the melt through continued partial melting will enclosed sulphides add their high [Os] and unradiogenic 187Os/188Os to the aggregate melt. Platinum-group element data for whole rocks are also consistent with this scenario. The sequence of (i) addition of all of the metasomatic sulphide, followed by (ii) the incorporation of small amounts of armoured sulphide can thus account for the range of both [Os] and 187Os/188Os of EM-basalts worldwide without the need for contributions from additional silicate mantle reservoirs.  相似文献   

6.
Lower crustal xenoliths recovered from Eocene to Cambrian kimberlites in the central and southern Slave craton are dominated by mafic granulites (garnet, clinopyroxene, plagioclase±orthopyroxene), with subordinate metatonalite and peraluminous felsic granulites. Geothermobarometry indicates metamorphic conditions of 650–800 °C at pressures of 0.9–1.1 GPa. The metamorphic conditions are consistent with temperatures expected for the lower crust of high-temperature low-pressure (HT-LP) metamorphic belts characteristic of Neoarchean metamorphism in the Slave craton. U–Pb geochronology of zircon, rutile and titanite demonstrate a complex history in the lower crust. Mesoarchean protoliths occur beneath the central Slave supporting models of an east-dipping boundary between Mesoarchean crust in the western and Neoarchean crust in the eastern Slave. At least, two episodes of igneous and metamorphic zircon growth occurred in the interval 2.64–2.58 Ga that correlate with the age of plutonism and metamorphism in the upper crust, indicating magmatic addition to the lower crust and metamorphic reworking during this period. In addition, discrete periods of younger zircon growth at ca. 2.56–2.55 and 2.51 Ga occurred 20–70 my after the cessation of ca. 2.60–2.58 Ga regional HT-LP metamorphism and granitic magmatism in the upper crust. This pattern of younger metamorphic events in the deep crust is characteristic of the Slave as well as other Archean cratons (e.g., Superior). The high temperature of the lower crust immediately following amalgamation of the craton, coupled with evidence for continued metamorphic zircon growth for >70 my after ‘stabilization’ of the upper crust, is difficult to reconcile with a thick (200 km), cool lithospheric mantle root beneath the craton prior to this event. We suggest that thick tectosphere developed synchronously or after these events, most likely by imbrication of mantle beneath the craton at or after ca. 2.6 Ga. The minimum age for establishing a cratonic like geotherm is given by lower crustal rutile ages of ca. 1.8 Ga in the southern Slave. Transient heating and possible magmatic additions to the lower crust continued through the Proterozoic, with possible additional growth of the tectosphere.  相似文献   

7.
Geochemistry and U-Pb ages of leucosomes and tonalites in a high pressure granulite unit of the Dulan area have been determined to constrain the tectonothermal evolution related to collision and thickening of lower crust in the North Qaidam Mountains (NQD). Leucosomes and tonalites show a marked chemical resemblance to adakites: (1) high La/Yb and Sr/Y, and low Y and HREE; (2) high Al2O3 and low Mg# values with obvious positive Eu anomalies; and (3) slightly positive εNd(t) values. Zircon U-Pb analysis of leucosomes and tonalites yielded 206Pb/238U ages of 428-437 Ma and 436-437 Ma respectively, which constrain the emplacement ages of the adakitic rocks. Petrological, geochronological and geochemical characters indicate that the adakitic rocks may have been derived from partial melting of a thickened mafic lower crust (> 50 km), suggesting a dominating source regime of synchronous high-pressure mafic granulites. Contemporary magmatism in other units of the NQD shows evidence of a widespread tectonothermal event during early Silurian (420-450 Ma) that includes metamorphism, magmatism and anatexis related to collision and thickening of lower crust.  相似文献   

8.
Shield-stage high-MgO alkalic lavas from La Palma and El Hierro (Canary Islands) have been characterized for their O-Sr-Nd-Os-Pb isotope compositions and major-, trace-, and highly siderophile-element (HSE: Os, Ir, Ru, Pt, Pd, Re) abundances. New data are also reported for associated evolved rocks, and entrained xenoliths. Clear differences in Pd/Ir and isotopic ratios for high Os (>50 ppt) lavas from El Hierro (δ18Oolivine = 5.17 ± 0.08‰; 87Sr/86Sr = 0.7029 to 0.7031; εNd = +5.7 to +7.1; 187Os/188Os = 0.1481 to 0.1750; 206Pb/204Pb = 19.1 to 19.7; Pd/Ir = 6 ± 3) versus those from La Palma (δ18Oolivine = 4.87 ± 0.18‰; 87Sr/86Sr = 0.7031 to 0.7032; εNd = +5.0 to +6.4; 187Os/188Os = 0.1421 to 0.1460; 206Pb/204Pb = 19.5 to 20.2; Pd/Ir = 11 ± 4) are revealed from the dataset.Crustal or lithospheric assimilation during magma transport cannot explain variations in isotopic ratios or element abundances of the lavas. Shallow-level crystal-liquid fractionation of olivine, clinopyroxene and associated early-crystallizing minerals (e.g., spinel and HSE-rich phases) controlled compatible element and HSE abundances; there is also evidence for sub-aerial degassing of rhenium. High-MgO lavas are enriched in light rare earth elements, Nb, Ta, U, Th, and depleted in K and Pb, relative to primitive mantle abundance estimates, typical of HIMU-type oceanic island basalts. Trace element abundances and ratios are consistent with low degrees (2-6%) of partial melting of an enriched mantle source, commencing in the garnet stability field (?110 km). Western Canary Island lavas were sulphur undersaturated with estimated parental melt HSE abundances (in ppb) of 0.07 ± 0.05 Os, 0.17 ± 0.16 Ir, 0.34 ± 0.32 Ru, 2.6 ± 2.5 Pt, 1.4 ± 1.2 Pd, 0.39 ± 0.30 Re. These estimates indicate that Canary Island alkali basalts have lower Os, Ir and Ru, but similar Pt, Pd and Re contents to Hawai’ian tholeiites.The HIMU affinities of the lavas, in conjunction with the low δ18Oolivine and high 206Pb/204Pb for La Palma, and elevated 187Os/188Os for El Hierro implies melting of different proportions of recycled oceanic crust and lithosphere. Our preferred model to explain isotopic differences between the islands is generation from peridotitic mantle metasomatised by <10% pyroxenite/eclogite made from variable portions of similar aged recycled oceanic crust and lithosphere. The correspondence of radiogenic 206Pb/204Pb, 187Os/188Os, elevated Re/Os and Pt/Os, and low-δ18O in western Canary Island lavas provides powerful support for recycled oceanic crust and lithosphere to generate the spectrum of HIMU-type ocean island basalt signatures. Persistence of geochemical heterogeneities throughout the stratigraphies of El Hierro and La Palma demonstrate long-term preservation of these recycled components in their mantle sources over relatively short-length scales (∼50 km).  相似文献   

9.
The Suwałki anorthosite massif, located in extreme northeast Poland beneath more than a kilometer of Phanerozoic cover, hosts major Fe-Ti-V deposits. These deposits, discovered in 1962, are contained in Fe and Ti oxide minerals that coexist with subordinate quantities of Fe, Cu, Ni, and Co sulfides in massif-style anorthosites, norites, and gabbronorites. Accessibility and other considerations preclude development of this natural resource in the present economic climate. Detailed work by Polish geologists during the last 35 years provides a sound geologic framework for this Re-Os study of the age and origin of oxide and sulfide deposits associated with a major, but lesser known anorthosite massif. Rhenium and osmium abundances and Os isotopic compositions were measured for nine sulfides and four titanomagnetites from the Suwałki anorthosite massif. The titanomagnetites are over an order of magnitude lower in Re (0.4–1.5 ppb) and Os (0.036–0.144 ppb) concentrations than co-precipitated pyrrhotite, pyrite, and chalcopyrite that yield consistent concentrations for Re (30–55 ppb) and Os (1–6 ppb). Parallel lines connecting co-existing titanomagnetite and sulfides have slopes of ∼1 on Re versus common Os concentration plots, indicating that both Re and Os behave similarly during crystallization in their high preference for any sulfide phase over magnetite. Samples from three deposits within the anorthosite massif were analyzed. An age of 1559 ± 37 Ma (n=10) with an initial 187Os/188Os of 1.16 ± 0.06 for the Jezioro Okrągłe and Krzemianka deposits is essentially identical to an age of 1556 ± 94 Ma (n=3) for the Udryń deposit. Udryń, however, yielded a marginally lower initial 187Os/188Os of 0.87 ± 0.20. The high initial 187Os/188Os combined with the Proterozoic Re-Os age indicates that the source for Suwałki oxides-sulfides is older crust, and hypothetically, could involve Archean rocks. An average crustal value of 50 for 187Re/188Os yields a 2777 Ma age for Suwałki source rocks. Widespread Phanerozoic cover severely limits knowledge of basement rocks in Poland, however, and no Archean rocks are known in the immediate region. More likely, 187Re/188Os ratios may be higher than average continental crust, reflecting mafic crust in the source, and may move the source age for Suwałki anorthosite and mineral deposits toward younger values that easily include ∼2.0 Ga Proterozoic rocks. This more favorable case also accommodates Paleoproterozoic Nd model ages. Regardless of Archean or Proterozoic source age, the high initial 187Os/188Os ratios derived from the Re-Os isochron indicate that the source for the oxide-sulfide mineral deposits is more likely the crust and not the mantle. Given that these deposits are clearly magmatic, the Re-Os results add a new dimension to the long-standing “origin of anorthosite” problem, implying a crustal source for the anorthosite as well. The 1559 Ma Suwałki age is compatible with a well-exposed east-west band of 1530-1660 Ma rapakivi granite-anorthosite magmatism to the immediate north, transecting western Russia, southern Finland, Estonia and Latvia, and central Sweden. In particular, the age and isotopic character of Suwałki are not unlike those of the well-studied Salmi rapakivi granite-anorthosite batholith in western Russia (Karelia). Received: 4 December 1998 / Accepted: 11 November 1999  相似文献   

10.
A method has been developed for the in situ determination of Re-Os isotopes in single grains of sulfides in mantle-derived peridotites using a laser ablation microprobe attached to a multicollector-induced coupled plasma mass spectrometer (MC-ICPMS). High-precision Os isotope analysis by MC-ICPMS is demonstrated by the measurement of interlaboratory Os standards. Evaluation of mass bias correction procedures shows that the exponential law provides the best fit to the Os isotope data and that the ratio of the mass fractionation coefficients for Re and Os remains constant for the range of typical instrument operating conditions. This relationship enables the accurate and precise correction of the isobaric interference of 187Re on 187Os for 187Re/188Os values up to 1.6.Results are presented for single sulfide inclusions in olivine macrocryts from kimberlites in the Siberian and Slave Cratons, and sulfides enclosed in silicates and interstitial to silicates in peridotite xenoliths from the Slave Craton and Massif Central, France. Enclosed sulfides larger than 50 μm in diameter and with Os contents ≥40 ppm give 187Os/188Os ratios with a precision of 0.1% (2 SE), which is equivalent to N-TIMS whole-rock data. Interstitial sulfides typically have lower Os (10 to 30 ppm) and give analyses with lower precision (∼1 to 2%) but still provide valuable information on the movement of Os within the lithosphere. The sulfide inclusions in silicates preserve significantly less radiogenic Os isotopic compositions than interstitial sulfides and accordingly produce significantly older and more realistic Re-Os age information. Whole-rock Os isotope compositions reflect the proportions of different generations of enclosed and interstitial sulfides; this calls into question the significance of many published “depletion ages.”  相似文献   

11.
Podiform chromite deposits occur in the mantle sequences of many ophiolites that were formed in supra-subduction zone (SSZ) settings. We have measured the Re-Os isotopic compositions of the major chromite deposits and associated mantle peridotites of the Dongqiao Ophiolite in the Bangong-Nujiang suture, Tibet, to investigate the petrogenesis of these rocks and their genetic relationships.The 187Os/188Os ratios of the chromite separates define a narrow range from 0.12318 to 0.12354, less variable than those of the associated peridotites. Previously-reported 187Os/188Os ratios of the Os-rich alloys enclosed in the chromitites define two clusters: 0.12645 ± 0.00004 (2 s; n = 145) and 0.12003 to 0.12194. The ultra-depleted dunites have much lower 187Os/188Os (0.11754, 0.11815), and the harzburgites show a wider range from 0.12107 to 0.12612. The average isotopic composition of the chromitites (187Os/188Os: 0.12337 ± 0.00001) is low compared with the carbonaceous chondrite value (187Os/188Os: 0.1260 ± 0.0013) and lower than the average value measured for podiform chromitites worldwide (0.12809 ± 0.00085). In contrast, the basalts have higher 187Os/188Os, ranging from 0.20414 to 0.38067, while the plagioclase-bearing harzburgite and cumulates show intermediate values of 187Os/188Os (0.12979 ~ 0.14206). Correspondingly, the basalts have the highest 187Re/188Os ratios, up to 45.4 ± 3.2, and the chromites have the lowest 187Re/188Os ratios, down to 0.00113 ± 0.00008. We suggest that melts/fluids, derived from the subducting slab, triggered partial melting in the overlying mantle wedge and added significant amounts of radiogenic Os to the peridotites. Mass-balance calculations indicate that a melt/mantle ratio of approximately 15:1 (melt: 187Re/188Os: 45.4, 187Os/188Os: 0.34484; mantle peridotite: 187Re/188Os: 0.0029, 187Os/188Os: 0.11754) is necessary to increase the Os isotopic composition of the chromitite deposits to its observed average value. This value implies a surprisingly low average melt/mantle ratio during the formation of the chromitite deposits. The percolating melts probably were of variable isotopic composition. However, in the chromitite pods the Os from many melts was pooled and homogenized, which is why the chromitite deposits show such a small variation in their Os isotopic composition. The results of this study suggest that the 187Os/188Os ratios of chromitites may not be representative of the DMM, but only reflect an upper limit. Importantly, the Os-isotope compositions of chromitites strongly suggest that such deposits can be formed by melt/mantle mixing processes.  相似文献   

12.
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   

13.
Using improved analytical techniques, which reduce the Re blanks by factors of 8 to 10, we report new Re-Os data on low Re and low PGE pallasites (PAL-anom) and IIIAB irons. The new pallasite samples nearly double the observed range in Re/Os for pallasites and allow the determination of an isochron of slope 0.0775 ± 0.0008 (T = 4.50 ± 0.04 Ga, using the adjusted λ187Re = 1.66 × 10−11 a−1) and initial (187Os/188Os)0 = 0.09599 ± 0.00046. If the data on different groups of pallasites (including the “anomalous” pallasites) are considered to define a whole-rock isochron, their formation would appear to be distinctly younger than for the iron meteorites by ∼60 Ma. Five IIIAB irons (Acuna, Bella Roca, Chupaderos, Grant, and Bear Creek), with Re contents ranging from 0.9 to 2.8 ppb, show limited Re/Os fractionation and plot within errors on the IIAB iron meteorite isochron of slope 0.07848 ± 0.00018 (T = 4.56 ± 0.01 Ga) and initial (187Os/188Os)0 = 0.09563 ± 0.00011. Many of the meteorites were analyzed also for Pd-Ag and show 107Ag enrichments correlated with Pd/Ag, requiring early formation and fractionation of the FeNi metal, in a narrow time interval, after injection of live 107Pd (t1/2 = 6.5 Ma) into the solar nebula. Based on Pd-Ag, the typical range in relative ages of these meteorites is ≤10 Ma. The Pd-Ag results suggest early formation and preservation of the 107Pd-107Ag systematics, both for IIIAB irons and for pallasites, while the younger Re-Os apparent age for pallasites suggests that the Re-Os system in pallasites was subject to re-equilibration. The low Re and low PGE pallasites show significant Re/Os fractionation (higher Re/Os) as the Re and PGE contents decrease. By contrast, the IIIAB irons show a restricted range in Re/Os, even for samples with extremely low Re and PGE contents. There is a good correlation of Re and Ir contents. The correlation of Re and Os contents for IIIAB irons shows a similar complex pattern as observed for IIAB irons (Morgan et al., 1995), and neither can be ascribed to a continuous fractional crystallization process with uniform solid-metal/liquid-metal distribution coefficients.  相似文献   

14.
A.G. Dessai  A. Markwick  H. Downes 《Lithos》2004,78(3):263-290
Granulite and pyroxenite xenoliths in lamprophyre dykes intruded during the waning stage of Deccan Trap volcanism are derived from the lower crust beneath the Dharwar craton of Western India. The xenolith suite consists of plagioclase-poor mafic granulites (55% of the total volume of xenoliths), plagioclase-rich felsic granulites (25%), and ultramafic pyroxenites and websterites (20%) with subordinate wehrlites. Rare spinel peridotite xenoliths are also present, representing mantle lithosphere. The high Mg #, low SiO2/Al2O3 and low Nb/La (<1) ratios suggest that the protoliths of the mafic granulites broadly represent cumulates of sub-alkaline magmas. All of the granulites are peraluminous and light rare-earth element-enriched. The felsic granulites may have resulted from anatexis of the mafic lower crustal rocks; thus, the mafic granulites are enriched in Sr whereas the felsic ones are depleted. Composite xenoliths consisting of mafic granulites traversed by veins of pyroxenite indicate intrusion of the granulitic lower crust by younger pyroxenites. Petrography and geochemistry of the latter (e.g. presence of phlogopite) indicate the metasomatised nature of the deep crust in this region.Thermobarometric estimates from phase equilibria indicate equilibration conditions between 650 and 1200 °C, 0.7-1.2 GPa suggestive of lower crustal environments. These estimates provide a spatial context for the sampled lithologies thereby placing constraints on the interpretation of geophysical data. Integration of xenolith-derived P-T results with Deep Seismic Soundings (DSS) data suggests that the pyroxenites and websterites are transitional between the lower crust and the upper mantle. A three-layer model for the crust in western India, derived from the xenoliths, is consistent with DSS data. The mafic nature of this hybrid lower crust contrasts with the felsic lower crustal composition of the south Indian granulite terrain.  相似文献   

15.
High-precision Pt-Re-Os and Sm-Nd isotope and highly siderophile element (HSE) and rare earth element (REE) abundance data are reported for two 2.7 b.y. old komatiite lava flows, Tony’s flow (TN) from the Belingwe greenstone belt, Zimbabwe, and the PH-II flow (PH) from Munro Township in the Abitibi greenstone belt, Canada. The emplaced lavas are calculated to have contained ∼25% (TN) and ∼28% (PH) MgO. These lavas were derived from mantle sources characterized by strong depletions in highly incompatible lithophile trace elements, such as light REE (Ce/SmN = 0.64 ± 0.02 (TN) and 0.52 ± 0.01 (PH), ε143Nd(T) = +2.9 ± 0.2 in both sources). 190Pt-186Os and 187Re-187Os isochrons generated for each flow yield ages consistent with respective emplacement ages obtained using other chronometers. The calculated precise initial 186Os/188Os = 0.1198318 ± 3 (TN) and 0.1198316 ± 5 (PH) and 187Os/188Os = 0.10875 ± 17 (TN) and 0.10873 ± 15 (PH) require time-integrated 190Pt/188Os and 187Re/188Os of 0.00178 ± 11 and 0.407 ± 8 (TN) and 0.00174 ± 18 and 0.415 ± 5 (PH). These parameters, which by far represent the most precise and accurate estimates of time-integrated Pt/Os and Re/Os of the Archean mantle, are best matched by those of enstatite chondrites. The data also provide evidence for a remarkable similarity in the composition of the sources of these komatiites with respect to both REE and HSE. The calculated absolute HSE abundances in the TN and PH komatiite sources are within or slightly below the range of estimates for the terrestrial Primitive Upper Mantle (PUM). Assuming a chondritic composition of the bulk silicate Earth, the strong depletions in LREE, yet chondritic Re/Os in the komatiite sources are apparently problematic because early Earth processes capable of fractionating the LREE might also be expected to fractionate Re/Os. This apparent discrepancy could be reconciled via a two-stage model, whereby the moderate LREE depletion in the sources of the komatiites initially occurred within the first 100 Ma of Earth’s history as a result of either global magma ocean differentiation or extraction and subsequent long-term isolation of early crust, whereas HSE were largely added subsequently via late accretion. The komatiite formation, preceded by derivation of basaltic magmas, was a result of second-stage, large-degree dynamic melting in mantle plumes.  相似文献   

16.
New major- and trace-element data of bulk-rocks and constituent minerals, and whole-rock Re-Os isotopic compositions of samples from the Lherz Massif, French Pyrenees, reveal complex petrological relationships between the dominant lithologies of lherzolite ± olivine-websterite and harzburgite. The Lherz peridotite body contains elongate, foliation parallel, lithological strips of harzburgite, lherzolite, and olivine-websterite cross-cut by later veins of hornblende-bearing pyroxenites. Peridotite lithologies are markedly bimodal, with a clear compositional gap between harzburgites and lherzolites ± olivine-websterite. Bulk-rock and mineral major-element oxide (Mg-Fe-Si-Cr) compositions show that harzburgites are highly-depleted and result from ∼20-25 wt.% melt extraction at pressures <2 GPa. Incompatible and moderately-compatible trace-element abundances of hornblendite-free harzburgites are analogous to some mantle-wedge peridotites. In contrast, lherzolites ± olivine-websterite overlap estimates of primitive mantle composition, yet these materials are composite samples that represent physical mixtures of residual lherzolites and clinopyroxene dominated cumulates equilibrated with a LREE-enriched tholeiitic melt. Trace-element compositions of harzburgite, and some lherzolite bulk-rocks and pyroxenes have been modified by; (1) wide-spread interaction with a low-volume LREE-enriched melt +/− fluid that has disturbed highly-incompatible elements (e.g., LREEs, Zr) without enrichment of alkali- and Ti-contents; and (2) intrusion of relatively recent, small-volume, hornblendite-forming, basanitic melts linked to modal and cryptic metasomatism resulting in whole-rock and pyroxene Ti, Na and MREE enrichment.Rhenium-Os isotope systematics of Lherz samples are also compositionally bimodal; lherzolites ± olivine-websterite have chondritc to suprachondritic 187Os/188Os and 187Re/188Os values that overlap the range reported for Earth’s primitive upper mantle, whereas harzburgites have sub-chondritic 187Os/188Os and 187Re/188Os values. Various Os-model age calculations indicate that harzburgites, lherzolites, and olivine-websterites have been isolated from convective homogenisation since the Meso-Proterozoic and this broadly coincides with the time of melt extraction controlled by harzburgite Os-isotope compositions. The association between harzburgites resulting from melting in mantle-wedge environments and Os-rich trace-phases (laurite-erlichmanite sulphides and Pt-Os-Ir-alloys) suggests that a significant portion of persistent refractory anomalies in the present-day convecting mantle of Earth may be linked to ancient large-scale melting events related to wide-spread subduction-zone processing.  相似文献   

17.
Pyroxenitic layers are a minor constituent of ultramafic mantle massifs, but are considered important for basalt generation and mantle refertilization. Mafic spinel websterite and garnet-spinel clinopyroxenite layers within Jurassic ocean floor peridotites from the Totalp ultramafic massif (eastern Swiss Alps) were analyzed for their highly siderophile element (HSE) and Os isotope composition.Aluminum-poor pyroxenites (websterites) display chondritic to suprachondritic initial γOs (160 Ma) of −2 to +27. Osmium, Ir and Ru abundances are depleted in websterites relative to the associated peridotites and to mantle lherzolites worldwide, but relative abundances (Os/Ir, Ru/Ir) are similar. Conversely, Pt/Ir, Pd/Ir and Re/Ir are elevated.Aluminum-rich pyroxenites (clinopyroxenites) are characterized by highly radiogenic 187Os/188Os with initial γOs (160 Ma) between +20 and +1700. Their HSE composition is similar to that of basalts, as they are more depleted in Os, Ir and Ru compared to Totalp websterites, along with even higher Pt/Ir, Pd/Ir and Re/Ir. The data are most consistent with multiple episodes of reaction of mafic pyroxenite precursor melts with surrounding peridotites, with the highest degree of interaction recorded in the websterites, which typically occur in direct contact to peridotites. Clinopyroxenites, in contrast, represent melt-dominated systems, which retained the precursor melt characteristics to a large extent. The melts may have been derived from a sublithospheric mantle source with high Pd/Ir, Pt/Ir and Re/Os, coupled with highly radiogenic 187Os/188Os compositions. Modeling indicates that partial melting of subducted, old oceanic crust in the asthenosphere could be a possible source for such melts.Pentlandite and godlevskite are identified in both types of pyroxenites as the predominant sulfide minerals and HSE carriers. Heterogeneous HSE abundances within these sulfide grains likely reflect subsolidus processes. In contrast, large grain-to-grain variations, and correlated variations of HSE ratios, indicate chemical disequilibrium under high-temperature conditions. This likely reflects multiple events of melt-rock interaction and sulfide precipitation. Notably, sulfides from the same thick section for the pyroxenites may display both residual-peridotite and melt-like HSE signatures. Because Totalp pyroxenites are enriched in Pt and Re, and depleted in Os, they will develop excess radiogenic 187Os and 186Os, compared to ambient mantle. These enrichments, however, do not possess the requisite Pt-Re-Os composition to account for the coupled suprachondritic 186Os-187Os signatures observed in some Hawaiian picrites, Gorgona komatiites, or the Siberian plume.  相似文献   

18.
The 187Os/188Os for 22 ureilite whole rock samples, including monomict, augite-bearing, and polymict lithologies, were examined in order to constrain the provenance and subsequent magmatic processing of the ureilite parent body (or bodies). The Re/Os ratios of most ureilites show evidence for a recent disturbance, probably related to Re mobility during weathering, and no meaningful chronological information can be extracted from the present data set. The ureilite 187Os/188Os ratios span a range from 0.11739 to 0.13018, with an average of 0.1258 ± 0.0023 (1σ), similar to typical carbonaceous chondrites, and distinct from ordinary or enstatite chondrites. The similar mean of 187Os/188Os measured for the ureilites and carbonaceous chondrites suggests that the ureilite parent body probably formed within the same region of the solar nebula as carbonaceous chondrites. From the narrow range of the 187Os/188Os distribution in ureilite meteorites it is further concluded that Re was not significantly fractionated from Os during planetary differentiation and was not lost along with the missing ureilitic melt component. The lack of large Re/Os fractionations requires that Re/Os partitioning was controlled by a metal phase, and thus metal had to be stable throughout the interval of magmatic processing on the ureilite parent body.  相似文献   

19.
Major elements, highly siderophile elements (HSE) and Re-Os isotope ratios were analysed in situ on individual sulfide grains in spinel peridotite xenoliths hosted by Miocene intraplate basalts from the Penghu Islands, Taiwan. The xenoliths represent texturally and compositionally different mantle domains, and the geochemical characteristics of the sulfides show changes in HSE distribution and Re-Os isotope systematics, produced as their host rocks were metasomatised by percolating fluids/melts. In prophyroclastic and partly metasomatised peridotites from the Kueipi (KP) locality, the sulfides have subchondritic to superchondritic 187Re/188Os and 187Os/188Os ratios. Many of these sulfides reflect fluid/melt interaction with residual MSS and/or crystallization of fractionated sulfide melts, which produced high contents of Cu and PPGEs and high Re/Os; inferred melt/rock ratios are low. In contrast, sulfides in equigranular and extensively metasomatised peridotites from the Tungchiyu (TCY) locality are mainly more sulfur-rich Ni-(Co)-rich MSS, with subchondritic to chondritic 187Os/188Os and subchondritic 187Re/188Os. These sulfides are interpreted as products of interaction between pre-existing MSS and percolating silicate melts. Melt/rock ratios were high and the percolating melt was less differentiated than the melt that percolated the KP peridotites. Sulfides in a TCY pyroxenite are mainly MSS; they have the lowest HSE contents, subchondritic to superchondritic 187Os/188Os and subchondritic 187Re/188Os, and may have precipitated from sulfide melts that segregated from basaltic melts under S-saturated conditions. In most sulfides melt percolation appears to have induced fractionation among the HSEs and disturbed Re-Os isotope compositions. Despite the metasomatic effects, rare residual MSS, sulfides that from crystallised sulfide melts and sulfides modified by addition of Re (with no evidence for Os addition) can still provide useful chronological information. Such sulfides yield TRD age peaks of 1.9, 1.7-1.6, 1.4-1.3 and 0.9-0.8 Ga, which may record the timing of melt extraction and/or metasomatic events in the mantle. These periods are contemporaneous with the major crustal events recorded by U-Pb dates and Nd and Hf model ages in the overlying crust. This close correspondence indicates that the sulfide TRD ages reflect the timing of lithosphere-scale tectonothermal events (such as melting and metasomatism) that affected both the lithospheric mantle and the overlying crust. The sulfide TRD ages, taken together with the crustal data, suggest that most of the Cathaysia block had formed at least by Paleo-Proterozoic time, and that some domains are Archean in age.  相似文献   

20.
《Chemical Geology》2007,236(3-4):323-338
Serpentinized garnet peridotites from the Xugou peridotite body of the Sulu ultrahigh-pressure (UHP) metamorphic terrane, central eastern China, are refractory (olivines have Fo91.7–93.1), indicating their origin as residual mantle. Negative correlations between whole-rock MgO and TiO2, Al2O3, total Fe2O3 and CaO (r = − 0.90 to − 0.95) and positive correlations between whole-rock Al2O3 and CaO and incompatible elements [Li, V, Cu, Ga, Sr, Y, Zr, heavy rare earth elements (HREEs), Hf, Pb and U] (r = 0.69 to 0.98) likely reflect melt depletion trends. Four highly refractory samples were selected for Re–Os isotopic analysis. Although they show evidence of variable enrichment of incompatible elements during serpentinization/metasomatism, no correlations exist between 187Re/188Os or 187Os/188Os with either La or Re (r = 0.00 to 0.17). These results indicate that any Re addition was fairly recent and did not affect the Os isotopic composition significantly. The correlation between 187Os/188Os and 187Re/188Os ratios thus, most likely reflects an ancient melt extraction event.The TRD, TMA and errorchron ages of the Xugou peridotites are all similar, suggesting that these peridotites formed around 2.0 Ga ago. This age is similar to Os model ages of mantle peridotites from the Dabie terrane, but contrasts markedly with the Archean ages of the continental lithospheric mantle (CLM) beneath the eastern block of the North China craton (NCC). If we assume that the Dabie–Sulu belt formed by the Triassic collision of the Yangtze craton with the eastern block of NCC and that the Archean aged CLM of the latter persisted until the Triassic, the Paleoproterozoic ages suggest derivation of these Dabie–Sulu mantle peridotites from the Yangtze craton. A Yangtze craton origin is consistent with the existing tectonic model of the Dabie–Sulu UHP belt. Our results support the hypothesis that the crust and underlying lithospheric mantle of the Yangtze craton were subducted to depths of > 180–200 km to form the world's largest UHP belt.  相似文献   

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