Compatibility of rhenium in garnet during mantle melting and magma genesis

Measurements of the partitioning of rhenium (Re) between garnet and silicate liquid from 1.5 to 2.0 gigapascals and 1250 degrees to 1350 degreesC show that Re is compatible in garnet. Oceanic island basalts (OIBs) have lower Re contents than mid-ocean ridge basalt, because garnet-bearing residues of deeper OIB melting will retain Re. Deep-mantle garnetite or eclogite may harbor the missing Re identified in crust-mantle mass balance calculations. Oceanic crust recycled into the upper mantle at subduction zones will retain high Re/Os (osmium) ratios and become enriched in radiogenic 187Os. Recycled eclogite in a mantle source should be easily traced using Re abundances and Os isotopes.     

Lu-Hf Isotope Systematics of Garnet Pyroxenites from Beni Bousera, Morocco: Implications for Basalt Origin

Six garnet pyroxenites from Beni Bousera, Morocco, yield a mean lutetium-hafnium age of 25 +/- 1 million years ago and show a wide range in hafnium isotope compositions (varepsilonHf = -9 to +42 25 million years ago), which exceeds that of known basalts (0 to +25). Therefore, primary melts of garnet pyroxenites cannot be the source of basalts. The upper mantle may be an aggregate of pyroxenites that were left by the melting of oceanic crust at subduction zones and peridotites that were contaminated by the percolation of melts from these pyroxenites. As a consequence, the concept of geochemical heterogeneities as passive tracers is inadequate. Measured lutetium-hafnium partitioning of natural minerals requires a reassessment of some experimental work relevant to mantle melting in the presence of garnet.     

Osmium isotopic evidence for ancient subcontinental lithospheric mantle beneath the kerguelen islands, southern indian ocean

Upper mantle xenoliths found in ocean island basalts are an important window through which the oceanic mantle lithosphere may be viewed directly. Osmium isotopic data on peridotite xenoliths from the Kerguelen Islands, an archipelago that is located on the northern Kerguelen Plateau in the southern Indian Ocean, demonstrate that pieces of mantle of diverse provenance are present beneath the Islands. In particular, peridotites with unradiogenic osmium and ancient rhenium-depletion ages (to 1.36 x 10(9) years old) may be pieces of the Gondwanaland subcontinental lithosphere that were incorporated into the Indian Ocean lithosphere as a result of the rifting process.     

A quantitative link between recycling and osmium isotopes

Recycled subducted ocean crust has been traced by elevated 187Os/188Os in some studies and by high nickel and low manganese contents in others. Here, we show that these tracers are linked for Quaternary lavas of Iceland, strengthening the recycling model. An estimate of the osmium isotopic composition of both the recycled crust and the mantle peridotite implies that Icelandic Quaternary lavas are derived in part from an ancient crustal component with model ages between 1.1 _ 109 and 1.8 _ 109 years and from a peridotitic end-member close to present-day oceanic mantle.     

182W evidence for long-term preservation of early mantle differentiation products

Late accretion, early mantle differentiation, and core-mantle interaction are processes that could have created subtle (182)W isotopic heterogeneities within Earth's mantle. Tungsten isotopic data for Kostomuksha komatiites dated at 2.8 billion years ago show a well-resolved (182)W excess relative to modern terrestrial samples, whereas data for Komati komatiites dated at 3.5 billion years ago show no such excess. Combined (182)W, (186,187)Os, and (142,143)Nd isotopic data indicate that the mantle source of the Kostomuksha komatiites included material from a primordial reservoir that represents either a deep mantle region that underwent metal-silicate equilibration or a product of large-scale magmatic differentiation of the mantle. The preservation, until at least 2.8 billion years ago, of this reservoir-which likely formed within the first 30 million years of solar system history-indicates that the mantle may have never been well mixed.     

Rhenium-osmium and samarium-neodymium isotopic systematics of the stillwater complex

Isotopic data for the Stillwater Complex, Montana, which formed about 2700 Ma (million years ago), were obtained to evaluate the role of magma mixing in the formation of strategic platinum-group element (PGE) ore deposits. Neodymium and osmium isotopic data indicate that the intrusion formed from at least two geochemically distinct magmas. Ultramafic affinity (U-type) magmas had initial epsilon(Nd) of -0.8 to -3.2 and a chondritic initial (187)Os/(186)Os ratio of approximately 0.88, whereas anorthositic affinity (A-type) magmas had epsilon(Nd) of -0.7 to +1.7 and an initial (187)Os/(186)Os ratio of approximately -1.13. These data suggest that U-type magmas were derived from a lithospheric mantle source containing recycled crustal materials whereas A-type magmas originated either by crustal contamination of basaltic magmas or by partial melting of basalt in the lower crust. The Nd and Os isotopic data also suggest that Os, and probably the other PGEs in ore horizons such as the J-M Reef, was derived from A-type magmas. The Nd and Os isotopic heterogeneity observed in rocks below the J-M Reef also suggests that A-type magmas were injected into the Stillwater U-type magma chamber at several stages during the development of the Ultramafic series.     

Coupled 186Os and 187Os evidence for core-mantle interaction

Osmium isotopic analyses of picritic lavas from Hawaii show enrichments in the osmium-186/osmium-188 ratio (186Os/188Os) of 0. 008 to 0.018%, relative to a chondritic upper mantle, that are positively correlated with enrichments in 187Os/188Os of 5.4 to 9.0%. The most viable mechanism to produce these coupled 186Os and 187Os enrichments is by addition of 0.5 to 1 weight percent of outer core metal to a portion of the D" layer and subsequent upwelling of the mixture. These data suggest that some plumes originate at the core-mantle boundary and that Os isotopes may be used to distinguish plumes derived from shallow versus deep mantle sources.     

Evidence for an ancient osmium isotopic reservoir in Earth

Iridosmine grains from placer deposits associated with peridotite-bearing ophiolites in the Klamath mountains have extremely radiogenic 186Os/188Os ratios and old Re-Os minimum ages, from 256 to 2644 million years. This indicates the existence of an ancient platinum group element reservoir with a supra-chondritic Pt/Os ratio. Such a ratio may be produced in the outer core as a result of inner core crystallization that fractionates Os from Pt. However, if the iridosmine Os isotopic compositions are a signature of the outer core, then the inner core must have formed very early, within several hundred million years after the accretion of Earth.     

142Nd evidence for early (>4.53 Ga) global differentiation of the silicate Earth

New high-precision samarium-neodymium isotopic data for chondritic meteorites show that their 142Nd/144Nd ratio is 20 parts per million lower than that of most terrestrial rocks. This difference indicates that most (70 to 95%) of Earth's mantle is compositionally similar to the incompatible element-depleted source of mid-ocean ridge basalts, possibly as a result of a global differentiation 4.53 billion years ago (Ga), within 30 million years of Earth's formation. The complementary enriched reservoir has never been sampled and is probably located at the base of the mantle. These data influence models of Earth's compositional structure and require revision of the timing of global differentiation on Earth's Moon and Mars.     

Genetic relations of oceanic basalts as indicated by lead isotopes

The isotopic compositions of lead and the concentrations lead, uranium, and thorium in samples of oceanic tholeiite and alkali suites are determined, and the genetic relations of the oceanic basalts are discussed. Lead of the oceanic tholeiites has a varying lead-206: lead-204 ratio between 17.8 and 18.8, while leads of the alkali basalt suites from Easter Island and Guadalupe Island are very radiogenic with lead-206: lead-204 ratios between 19.3 and 20.4 It is concluded that (i) the isotopic composition of lead in oceanic tholeiite suggests that the upper mantle source region of the tholeiite was differentiated from and original mantle material more than 1 billion years ago and that the upper mantle is not homogeneous at the present time, (ii) less than 20 million years was required for the crystal differentiation within the alkali suite from Easter Island, (iii) no crustal contamination was involved in the course of differentiation of rocks from Easter Island; however, some crustal contamination may have affected Guadalupe Island rocks, and (iv) alkali basalt may be produced from the tholeiite in the oceanic region by crystal differentiation. Alternatively the difference in the isotopic composition of lead in oceanic basalts may be produced by partial melting at different depths of a differentiated upper mantle.     

Osmium Recycling in Subduction Zones

Peridotite xenoliths from the Cascade arc in the United States and in the Japan arc have neodymium and osmium isotopic compositions that are consistent with addition of 5 to 15 percent of subducted material to the present-day depleted mantle. These observations suggest that osmium can be partitioned into oxidized and chlorine-rich slab-derived fluids or melts. These results place new constraints on the behavior of osmium (and possibly other platinum group elements) during subduction of oceanic crust by showing that osmium can be transported into the mantle wedge.     

Rhenium-osmium isotope constraints on the age of iron meteorites

Rhenium and osmium concentrations and the osmium isotopic compositions of iron meteorites were determined by negative thermal ionization mass spectrometry. Data for the IIA iron meteorites define an isochron with an uncertainty of approximately +/-31 million years for meteorites approximately 4500 million years old. Although an absolute rheniumosmium closure age for this iron group cannot be as precisely constrained because of uncertainty in the decay constant of (187)Re, an age of 4460 million years ago is the minimum permitted by combined uncertainties. These age constraints imply that the parent body of the IIAB magmatic irons melted and subsequently cooled within 100 million years after the formation of the oldest portions of chondrites. Other iron meteorites plot above the IIA isocbron, indicating that the planetary bodies represented by these iron groups may have cooled significantly later than the parent body of the IIA irons.     

Orphan strontium-87 in abyssal peridotites: daddy was a granite

The (87)Sr/(86)Sr ratios in some bulk abyssal and alpine peridotites are too high to be binary mixtures of depleted mantle and seawater components. The apparent excess, or "orphan," (87)Sr appears to be separated from its radioactive parent. Such observations were widely held to be analytical artifacts. Study of several occurrences of orphan (87)Sr shows that the orphan component in abyssal peridotite is located in the alteration products of olivine and enstatite in the peridotite. The orphan (87)Sr is most likely introduced by infiltration of low-temperature (<200 degrees C) seawater bearing suspended detrital particulates. These particulates include grains of detrital clay that are partly derived from continental (that is, granitic) sources and thus are highly radiogenic. Orphan (87)Sr and other radiogenic isotopes may provide a tracer for low-temperature seawater penetrating into the oceanic crust.     

Rhenium-osmium isotope systematics of carbonaceous chondrites

Rhenium and osmium concentrations and Os isotopic compositions of eight carbonaceous chondrites, one LL3 ordinary chondrite, and two iron meteorites were determined by resonance ionization mass spectrometry. Iron meteorite (187)Re/(186)Os and (l87)Os/(l86)Os ratios plot on the previously determined iron meteorite isochron, but most chondrite data plot 1 to 2 percent above this meteorite isochron. This suggests either that irons have significantly younger Re-Os closure ages than chondrites or that chondrites were formed from precursor materials with different chemical histories from the precursors of irons. Some samples of Semarkona (LL3) and Murray (C2M) meteorites plot 4 to 6 percent above the iron meteorite isochron, well above the field delineated by other chondrites. Murray may have lost Re by aqueous leaching during its preterrestrial history. Semarkona could have experienced a similar loss of Re, but only slight aqueous alteration is evident in the meteorite. Therefore, the isotopic composition of Semarkona could reflect assembly of isotopically heterogeneous components subsequent to 4.55 billion years ago or Os isotopic heterogeneities in the primordial solar nebula.     

A major meteorite impact on the Earth 65 million years ago: evidence from the cretaceous-tertiary boundary clay

Evidence for a major meteorite impact on the earth 65 million years ago is shown by the presence of meteoritic debris in the "fish clay" from Denmark representing the Cretaceous-Tertiary boundary. Noble metals (iridium, osmium, gold, platinum, rhenium, ruthenium, palladium, nickel, and cobalt), which are sensitive indicators of meteorites and are normally depleted on the terrestrial surface by factors of 10(4) to 10(2) relative to cosmic abundances, are enriched in this boundary clay by factors of 5 to 100 over the expected abundances. With the exception of rhenium, all the enriched noble metals in the clay are present in cosmic proportions, indicating that the impacting celestial body had not undergone gross chemical differentiation. The major extinction of life on the earth at the end of the Cretaceous Period may be related to the meteorite impact.     

High-3He Plume Origin and Temporal-Spatial Evolution of the Siberian Flood Basalts

An olivine nephelinite from the lower part of a thick alkalic ultrabasic and mafic sequence of volcanic rocks of the northeastern part of the Siberian flood basalt province (SFBP) yielded a (40)Ar/(39)Ar plateau age of 253.3 +/- 2.6 million years, distinctly older than the main tholeiitic pulse of the SFBP at 250.0 million years. Olivine phenocrysts of this rock showed (3)He/(4)He ratios up to 12.7 times the atmospheric ratio; these values suggest a lower mantle plume origin. The neodymium and strontium isotopes, rare earth element concentration patterns, and cerium/lead ratios of the associated rocks were also consistent with their derivation from a near-chondritic, primitive plume. Geochemical data from the 250-million-year-old volcanic rocks higher up in the sequence indicate interaction of this high-(3)He SFBP plume with a suboceanic-type upper mantle beneath Siberia.     

Diamonds and the african lithosphere

Data and inferences drawn from studies of diamond inclusions, xenocrysts, and xenoliths in the kimberlites of southern Africa are combined to characterize the structure of that portion of the Kaapvaal craton that lies within the mantle. The craton has a root composed in large part of peridotites that are strongly depleted in basaltic components. The asthenosphere boundary shelves from depths of 170 to 190 kilometers beneath the craton to approximately 140 kilometers beneath the mobile belts bordering the craton on the south and west. The root formed earlier than 3 billion years ago, and at that time ambient temperatures in it were 900 degrees to 1200 degrees C; these temperatures are near those estimated from data for xenoliths erupted in the Late Cretaceous or from present-day heat-flow measurements. Many of the diamonds in southern Africa are believed to have crystallized in this root in Archean time and were xenocrysts in the kimberlites that brought them to the surface.     

Water in Earth's Mantle: The Role of Nominally Anhydrous Minerals

Most minerals of Earth's upper mantle contain small amounts of hydrogen, structurally bound as hydroxyl (OH). The OH concentration in each mineral species is variable, in some cases reflecting the geological environment of mineral formation. Of the major mantle minerals, pyroxenes are the most hydrous, typically containing approximately 200 to 500 parts per million H(2)O by weight, and probably dominate the water budget and hydrogen geochemistry of mantle rocks that do not contain a hydrous phase. Garnets and olivines commonly contain approximately 1 to 50 parts per million. Nominally anhydrous minerals constitute a significant reservoir for mantle hydrogen, possibly accommodating all water in the depleted mantle and providing a possible mechanism to recycle water from Earth's surface into the deep mantle.     

Long-term sea-level fluctuations driven by ocean basin dynamics

Earth's long-term sea-level history is characterized by widespread continental flooding in the Cretaceous period (approximately 145 to 65 million years ago), followed by gradual regression of inland seas. However, published estimates of the Late Cretaceous sea-level high differ by half an order of magnitude, from approximately 40 to approximately 250 meters above the present level. The low estimate is based on the stratigraphy of the New Jersey margin. By assimilating marine geophysical data into reconstructions of ancient ocean basins, we model a Late Cretaceous sea level that is 170 (85 to 270) meters higher than it is today. We use a mantle convection model to suggest that New Jersey subsided by 105 to 180 meters in the past 70 million years because of North America's westward passage over the subducted Farallon plate. This mechanism reconciles New Jersey margin-based sea-level estimates with ocean basin reconstructions.     

Direct measurement of femtomoles of osmium and the 187Os/186Os ratio in seawater

Two depth profiles of the osmium concentration and the 187Os/186Os isotopic ratio in the Indian Ocean showed that the osmium concentration seems to be unaltered by chemical or biological processes occuring in seawater; accordingly, osmium is conservative. These data were obtained from an experimental method that eliminated the problems related to osmium preconcentration. This method led to a new evaluation of the concentration of osmium in seawater; the mean concentration of osmium and the 187Os/186Os ratio are equal to 10.86 +/- 0.07 picograms per kilogram and 8.80 +/- 0.07, respectively. The results suggest the existence of an organocomplex that dominates the speciation of osmium in seawater.