首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 125 毫秒
1.
In an effort to resolve the current conflict between geochemical requirements for an apparently isolated mantle reservoir and recent geophysical evidence for whole-mantle convection, we investigate the possibility that the region above the core-mantle boundary, termed D″, serves as an early-isolated, rare-gas- and incompatible-element-bearing reservoir, and we propose a mechanism for its formation that is a likely outcome of Earth accretion models. In these models, the most cataclysmic event in Earth history, the moon-forming giant impact on the proto-Earth of a Mars-size planet (perhaps as early as 4540 Ma ago) was followed by accretion of smaller bodies long afterwards (until ∼3900 Ma). Some collisions probably triggered melting, metal segregation and degassing. However, the small bodies, fragments, particles, dust, including those of chondrite-like composition, existed on near-earth orbits, were irradiated by intense solar wind, and finally fell on an early-formed, incompatible-element-enriched basaltic crust without causing extensive melting. The respective regions of the crust, loaded with chondrite-like debris, were therefore significantly enriched in iron. When this mixed material was subducted, the bulk density of the subducted lithosphere exceeded that of the bulk silicate mantle, which had already lost its metallic iron to the core. Segregation of this denser material at the base of the mantle was facilitated by the high temperatures at the core-mantle boundary, which greatly reduce the viscosity, as was quantitatively modelled by Christensen and Hofmann (Christensen, U.R., Hofmann, A.W., 1994. Segregation of subducted oceanic-crust in the convecting mantle. J. Geophys. Res.-Solid Earth 99 (B10), 19867–19884). Assuming a basalt/chondrite mass ratio of about 4/1, we obtain a density contrast of ∼7%, which would stabilize the subducted material between the metal core and silicate mantle.Mass balance considerations and preliminary results of geochemical modelling of the above scenario (similar to that performed by Tolstikhin and Marty [Tolstikhin, I.N., Marty, B., 1998. The evolution of terrestrial volatiles, A view from helium, neon, argon and nitrogen isotope modeling. Chem. Geol. 147, 27–52]) show the potential geochemical importance of D″. (1) Modelling of Pu–U–I–Xe isotope systematics predicts formation of this reservoir early in Earth history, ∼100 Ma after formation of the Solar system. (2) The total amount of heat-generating U, Th, K (and other highly incompatible elements) in D″ exceeds 20% of the Earth inventory, and a similar portion of terrestrial heat is being transferred from the core + D″ into the base of the overlying convecting mantle. (3) D″ is enriched in solar implanted rare gases because the small (re)-accreting debris with high surface/mass ratios will have been subjected to intense radiation by the early sun. (4) Rare gases diffuse from D″ into the overlying mantle and are then transferred into upwelling plumes, which originate above D″. In addition, small amounts of D″ material may be entrained by the mantle convective flow as was recently discussed by Schott et al. [Schott, B., Yuen, D.A., Braun, A., 2002. The influences of composition and temperature-dependent rheology in thermal-chemical convection on entrainment of the D″ layer. Physics Earth Planet. Inter. 129, 43–65]. From the rare-gas modelling it follows that initially (∼4500 Ma ago) D″ could have been more massive by a factor of ∼1.2 than at present (about 2 × 1026 g). The present-day mass flux from D″ into the convecting mantle is estimated to be ≤0.05 × 1016 g year−1, a factor of ∼100 less than the rate of ridge magmatism. This small contribution of D″ material makes it difficult to trace fingerprints of D″ even using such sensitive tracers as Pb isotope ratios. (5) The density contrast that stabilizes D″ is maintained by its higher intrinsic density due to the iron-rich chondrite-like component. Subduction of this material, its entrainment by convective mantle flow and mixing could also account for the preservation of the chondritic relative abundances of siderophile elements in the mantle. If D″ is partially molten, the density contrast may be caused by a high-density melt fraction.  相似文献   

2.
In order to better understand the nature and formation of oceanic lithosphere beneath the Early Cretaceous Ontong Java Plateau, Re–Os isotopes have been analysed in a suite of peridotite xenoliths from Malaita, Solomon Islands. Geological, thermobarometric and petrological evidence from previous studies reveal that the xenoliths represent virtually the entire thickness of the southern part of subplateau lithospheric mantle (< 120 km). This study demonstrates that vertical Os isotopic variations correlate with compositional variations in a stratified lithosphere. The shallowest plateau lithosphere (< 85 km) is dominated by fertile lherzolites showing a restricted range of 187Os/188Os (0.1222 to 0.1288), consistent with an origin from ~ 160 Ma Pacific lithosphere. In contrast, the basal section of subplateau lithospheric mantle (~ 95–120 km) is enriched in refractory harzburgites with highly unradiogenic 187Os/188Os ratios ranging from 0.1152 to 0.1196, which yield Proterozoic model ages of 0.9–1.7 Ga. Although the whole range of Os isotope compositions of Malaita peridotites is within the variations seen in modern abyssal peridotites, the contrasting isotopic compositions of shallow and deep plateau lithosphere suggest their derivation from different mantle reservoirs. We propose that the subplateau lithosphere forms a genetically unrelated two-layered structure, comprising shallower, typical oceanic lithosphere underpinned by deeper impinged material, which included a component of recycled Proterozoic lithosphere. The impingement of residual but chemically heterogeneous mantle, mechanically coupled to the recently formed, thin lithosphere, may have a bearing on the anomalous initial uplift and late subsidence history of the seismically anomalous plateau root.  相似文献   

3.
The distribution of extraterrestrial chromite grains (> 63 μm) has been studied in the resurge deposit of the early Late Ordovician (458 Ma) Lockne impact structure in central Sweden. A 1-kg-sample of resurge sediment from the rim of the crater is extremely rich in extraterrestrial chromite. In total the sample contains > 125 chromium spinel grains kg− 1, most grains being chromite. Due to post-depositional alterations, the origin of several of the grains is dubious, although it is clear that the major part of the chromites is of extraterrestrial origin (> 75 grains kg− 1), most likely derived from the impactor. The alterations are primarily due to the hydrothermal system induced by the impactor, with zinc enrichment in the chromites as the most common characteristic. The element chemistry of the least altered chromite grains indicates that the impactor was an ordinary L chondrite. This concurs with a suggested increase in the flux of L chondritic asteroids to Earth, following the disruption of the L chondrite parent body at ca. 470 Ma.More than 170 impact craters are known from around the Earth, but only few of the impactors have been identified, mainly due to the low survival rate of projectile material. Further studies of impact craters will reveal if survival of extraterrestrial chromite is unique for the Lockne structure.  相似文献   

4.
The Earth's mantle is chemically and isotopically heterogeneous, and a component of recycled oceanic crust is generally suspected in the convecting mantle [Hofmann and White, 1982. Mantle plumes from ancient oceanic crust. Earth Planet. Sci. Lett. 57, 421–436]. Indeed, the HIMU component (high µ = 238U/204Pb), one of four isotopically distinct end-members in the Earth's mantle, is generally attributed to relatively old (≥ 1–2 Ga) recycled oceanic crust in the form of eclogite/pyroxenite, e.g. [Zindler and Hart, 1986. Chemical geodynamics. Ann. Rev. Earth Planet. Sci. 14, 493–571]. Although the presence of the recycled component is generally supported by element and isotopic data, little is known about its physical state at mantle depths. Here we show that the concentrations of Ni, Mn and Ca in olivine from the Canarian shield stage lavas, which can be used to assess the physical nature of the source material (peridotite versus olivine-free pyroxenite) [Sobolev et al., 2007. The amount of recycled crust in sources of mantle-derived melts. Science 316, 412–417], correlate strongly with bulk rock Sr, Nd and Pb isotopic ratios. The most important result following from our data is that the enriched, HIMU-type (having higher 206Pb/204Pb than generally found in the other mantle end-members) signature of the Canarian hotspot magmas was not caused by a pyroxenite/eclogite constituent of the plume but appears to have been primarily hosted by peridotite. This implies that the old (older than ~ 1 Ga) ocean crust, which has more evolved radiogenic isotope compositions, was stirred into/reacted with the mantle so that there is not significant eclogite left, whereas younger recycled oceanic crust with depleted MORB isotopic signature (< 1 Ga) can be preserved as eclogite, which when melted can generate reaction pyroxenite.  相似文献   

5.
In situ LA-ICPMS U-Pb, trace element, and Hf isotope data in zircon demonstrate a Carboniferous age for eclogite-facies metamorphism in Siluro-Devonian protoliths in the Huwan shear zone, Dabie Mountains, Central China. This age contrasts with the more prevailing Triassic age for high- to ultrahigh pressure (HP to UHP) metamorphism in the Qinling-Dabie-Sulu orogen. Metamorphic zircon in two eclogite samples from Sujiahe is characterized by low Th/U ratios, small negative Eu anomalies, flat HREE patterns, and low 176Lu/177Hf ratios. These geochemical signatures suggest that the zircon crystallized in the presence of garnet and in the absence of plagioclase feldspar. Furthermore, temperatures of ~ 655 and ~ 638 °C, calculated using the Ti content of zircon, are consistent with their formation during eclogite-facies metamorphism. The weighted mean 206Pb/238U age of 309 ± 4 Ma (2δ) for this zircon improves previous age estimates for eclogite-facies metamorphism in the Huwan shear zone, ranging from 420 to 220 Ma. Metamorphic zircon from one eclogite sample from Hujiawan, most likely formed during prograde metamorphism, yields an equivalent age estimate of 312 ± 11 Ma. Magmatic zircon cores in the three samples yield ages for the magmatic protoliths of the eclogites ranging from 420 ± 7 to 406 ± 5 Ma, and post-dating the middle Paleozoic collision of the North China and the Qinling terrain. The zircon crystals in the three eclogite samples display a large variation of εHf (t) values of ? 4.9 to 21.3. The metamorphic zircon overgrowths show the same range of εHf (t) values as those of the inherited magmatic crystal interiors. This suggests that the metamorphic zircon overgrowths may have formed by dissolution-reprecipitation of pre-existing magmatic zircon thereby preserving their original Hf isotopic composition. The high εHf (t) values suggest that the protoliths were derived from depleted mantle sources, most likely Paleotethyan oceanic crust; while the low εHf (t) values are attributed to crustal contamination. Some eclogites in the Huwan shear zone have a distinctive signature of continental crust most probably derived from the Yangtze Craton. The coexistence of Paleozoic oceanic crust and Neoproterozoic continental crust with similar metamorphic ages in the Huwan shear zone implies that Paleozoic Paleotethyan oceanic crust was produced within a marginal basin of the northern Yangtze Craton. The opening of the Paleo-Tethyan ocean was slightly younger than the collision of the North China Craton and the Qinling terrain during the Late Paleozoic in the Qinling-Dabie-Sulu orogen. Subduction of the Paleo-Tethyan oceanic crust and associated continental basement resulted in the 309 ± 2 Ma (2σ) eclogite-facies metamorphism in the Huwan shear zone. The subsequent Triassic continent-continent collision led to the final coalescence of the Yangtze and Sino-Korean cratons. Amalgamation of the Yangtze and North China cratons was, therefore, a multistage process extending over at least 200 Ma.  相似文献   

6.
Atmospheric noble gases (e.g., 22Ne, 36Ar, 84Kr, 130Xe) in crustal fluids are only sensitive to subsurface physical processes. In particular, depletion of atmospheric noble gases in groundwater due to boiling and steam separation is indicative of the occurrence of a thermal event and can thus be used to trace the thermal history of stable tectonic regions. We present noble gas concentrations of 38 deep brines (~ 0.5–3.6 km) from the Michigan Basin. The atmospheric noble gas component shows a strong depletion pattern with respect to air saturated water. Depletion of lighter gases (22Ne and 36Ar) is stronger compared to the heavier ones (84Kr and 130Xe). To understand the mechanisms responsible for this overall atmospheric noble gas depletion, phase interaction models were tested. We show that this atmospheric noble gas depletion pattern is best explained by a model involving subsurface boiling and steam separation, and thus, consistent with the occurrence of a past thermal event of mantle origin as previously indicated by both high 4He/heat flux ratios and the presence of primordial mantle He and Ne signatures in the basin. Such a conceptual model is also consistent with the presence of past elevated temperatures in the Michigan Basin (e.g., ~ 80–260 °C) at shallow depths as suggested by previous thermal studies in the basin. We suggest that recent reactivation of the ancient mid-continent rift system underneath the Michigan Basin is likely responsible for the release of both heat and mantle noble gases into the basin via deep-seated faults and fracture zones. Relative enrichment of atmospheric Kr and Xe with respect to Ar is also observed, and is interpreted as reflecting the addition of sedimentary Kr and Xe from associated hydrocarbons, following the hydrothermal event. This study pioneers the use of atmospheric noble gases in subsurface fluids to trace the thermal history of stable tectonic regions.  相似文献   

7.
The geochemical characteristics of mildly alkalic basalts (24–25 Ma) erupted in the southeastern Kerguelen Archipelago are considered to represent the best estimate for the composition of the enriched Kerguelen plume end-member. A recent study of picrites and high-MgO basalts from this part of the archipelago highlighted the Pb and Hf isotopic variations and suggested the presence of mantle heterogeneities within the Kerguelen plume itself. We present new helium and neon isotopic compositions for olivines from these picrites and high-MgO basalts (6–17 wt.% MgO) both to constrain the enriched composition of the Kerguelen plume and to determine the origin of isotopic heterogeneities involved in the genesis of Kerguelen plume-related basalts. The olivine phenocrysts have extremely variable 4He / 3He compositions between MORB and primitive values observed in OIB (∼90,000 to 40,000; i.e., R / Ra ∼8 to 18) and they show primitive neon isotopic ratios (average 21Ne / 21Neext ∼0.044). The neon isotopic systematics and the 4He / 3He ratios that are lower than MORB values for the Kerguelen basalts clearly suggest that the Kerguelen hotspot belongs to the family of primitive hotspots, such as Iceland and Hawaii. The rare gas signature for the Kerguelen samples, intermediate between MORB and solar, is apparently inconsistent with mixing of a primitive component with a MORB-like source, but may result from sampling a heterogeneous part of the mantle with solar 3He / 22Ne and with a higher (U, Th) / 3He ratio compared to typically high R / Ra hotspot basalts such as those from Iceland and Hawaii.  相似文献   

8.
The transition from the early Pliocene “Warmhouse” towards the present “Icehouse” climate and the role of Gateway dynamics are intensively debated. Both, the constrictions of the Central American Seaway and the Indonesian Gateway affected ocean circulation and climate during the Pliocene epoch. Here, we use combined δ18O and Mg/Ca ratios of planktonic foraminifera (marine protozoa) from surface and subsurface levels to reconstruct the thermal structure and changes in salinities from the Southwest Pacific Deep Sea Drilling Project (DSDP) Site 590B from 6.5 to 2.5 Ma. Our data suggest a gradual cooling of ~ 2 °C and freshening of the sea surface during ~ 4.6–4 Ma with an increased meridional temperature gradient between the West Pacific Warm Pool and the Southwest Pacific when the closing of the Central American Seaway reached a critical threshold. After ~ 3.5 Ma, the restricted Indonesian Gateway might have amplified the East Australian Current, allowing enhanced heat transport towards the Southwest Pacific with reduced meridional temperature gradients when the global climate gradually cooled. At the same time our data suggest a cooling and freshening of Subantarctic Mode Water (SAMW) or/and an increased northward flow of SAMW towards Site 590B, possibly a first step towards the present Antarctic Frontal System.  相似文献   

9.
We report volatile (H2O, CO2, F, S, Cl) and trace element data for submarine alkalic basalt glasses from the three youngest Samoan volcanoes, Ta'u, Malumalu and Vailulu'u. Most samples are visibly sulfide saturated, so have likely lost some S during fractionation. Cl / K ratios (0.04–0.15) extend to higher values than pristine MORBs, but are suspected to be partly due to source differences since Cl / K roughly varies as a function of 87Sr / 86Sr. There are no resolvable differences in the relative enrichment of F among sources, and compatibility of F during mantle melting is established to be nearly identical to Nd. Shallow degassing has affected CO2 in all samples, and H2O only in the most shallowly erupted samples from Vailulu'u. Absolute water contents are high for Samoa (0.63–1.50 wt.%), but relative enrichment of water compared to equally incompatible trace elements (Ce, La) is low and falls entirely below normal MORB values. H2O / Ce (58–157) and H2O / La (120–350) correlate inversely with 87Sr / 86Sr compositions (0.7045–0.7089). This leads us to believe that, because of very fast diffusion of hydrogen in mantle minerals, recycled lithospheric material with high initial water and trace element content will lose water to the drier ambient mantle during storage within the inner Earth. The net result is the counter-intuitive appearance of greater dehydration with greater mantle enrichment. We expect that subducted slabs will experience a two-stage dehydration history, first within subduction zones and then in the ambient mantle during long-term convective mixing.  相似文献   

10.
Unlike other lakes in the McMurdo Dry Valleys, Antarctica, Lake Vida has a thick (~ 19 m) ice cover sealing a liquid brine body of unusually high salinity (~ 245 g/L) from the atmosphere. To constrain the conditions under which the atypical Lake Vida ice cover formed and evolved, 19 ice samples were collected down to a depth of ~ 14 m, together with three brine samples trapped in the ice at ~ 16 m for analysis of helium, neon, argon, krypton, and xenon concentrations. The broad pattern of noble gas concentrations for Lake Vida samples is fundamentally different from that of air saturated water (ASW) at 0 °C and an elevation of 340 m for salinities of 0 (ice) and 245 g/L (brine). Overall, ice samples are enriched in He and depleted in Ne with saturation relative to ASW averages of 1.38 and 0.82, respectively, and strongly depleted in Ar, Kr, and Xe with relative saturations of 0.10, 0.06, and 0.05, respectively. By contrast, brine samples are generally depleted in He and Ne (relative saturation averages of 0.33 and 0.27, respectively) but enriched in Ar, Kr, and Xe, with relative saturation averages of 1.45, 3.15, and 8.86, respectively. A three-phase freezing partitioning model generating brine, ice and bubble concentrations for all stable noble gases was tested and compared with our data. Measured brine values are best reproduced for a salinity value of 175 g/L, a pressure of 1.1 atm, and a bubble volume of 20 cm3 kg?1. Sensitivity tests for ice + bubble samples show an ideal fit for bubble volumes of ~ 1–2 cm3 kg?1. Our results show that the conditions under which ice and brine formed and evolved at Lake Vida are significantly different from other ice-covered lakes in the area. Our brine data suggest that Lake Vida may be transitioning from a wet to a dry-based lake, while the ice + bubble data suggest at least partial re-equilibration of residual liquid with the atmosphere as ice forms at the top of Lake Vida ice cover.  相似文献   

11.
The 1.0 Ma Kidnappers supereruption (~ 1200 km3 DRE) from Mangakino volcanic centre, Taupo Volcanic Zone, New Zealand, produced a large phreatomagmatic fall deposit followed by an exceptionally widespread ignimbrite. Detailed sampling and analysis of glass shards and mineral phases have been undertaken through a proximal 4.0 m section of the fall deposit, representing the first two-thirds of erupted extra-caldera material. Major and trace element chemistries of glass shards define three distinct populations (types A, B and C), which systematically change in proportion through the fall deposit and are inferred to represent three magma types. Type B glass and biotite first appear at the same level (~ 0.95 m above base) in the fall deposit suggesting later tapping of a biotite-bearing magma. Plagioclase and Fe–Ti oxide compositions show bimodal distributions, which are linked to types A and B glass compositions. Temperature and pressure (T–P) estimates from hornblende and Fe–Ti oxide equilibria from each magma type are similar and therefore the three magma bodies were adjacent, not vertically stacked, in the crust. Most hornblende model T–P estimates range from 770 to 840 °C and 90 to 170 MPa corresponding to storage depths of ~ 4.0–6.5 km. Hornblende model T–P estimates coupled with in situ trace element fingerprinting imply that the magma bodies were individually well mixed, and not stratified. Compositional gaps between the three glass compositional types imply that no mixing between these magmas occurred. We interpret these data, coupled with the systematic changes in shard compositional proportions through the fall deposit, to reflect that three independent melt-dominant bodies of magma contributed large (A, ~ 270 km3), medium (B, ~ 90 km3) and small (C, ~ 40 km3) volumes (as reflected in the fall deposits) and were systematically tapped during the eruption. We propose that the systematic evacuation of the three independent magma bodies implies that there was tectonic triggering and linkage of eruptions. Our results show that supereruptions can be generated by near simultaneous multiple eruptions from independent magma chambers rather than the evacuation of a large single unitary magma chamber.  相似文献   

12.
Coupled 187Os/188Os and highly siderophile element (HSE: Os, Ir, Ru, Pt, Pd, and Re) abundance data are reported for pristine lunar crustal rocks 60025, 62255, 65315 (ferroan anorthosites, FAN) and 76535, 78235, 77215 and a norite clast in 15455 (magnesian-suite rocks, MGS). Osmium isotopes permit more refined discrimination than previously possible of samples that have been contaminated by meteoritic additions and the new results show that some rocks, previously identified as pristine, contain meteorite-derived HSE. Low HSE abundances in FAN and MGS rocks are consistent with derivation from a strongly HSE-depleted lunar mantle. At the time of formation, the lunar floatation crust, represented by FAN, had 1.4 ± 0.3 pg g? 1 Os, 1.5 ± 0.6 pg g? 1 Ir, 6.8 ± 2.7 pg g? 1 Ru, 16 ± 15 pg g? 1 Pt, 33 ± 30 pg g? 1 Pd and 0.29 ± 0.10 pg g? 1 Re (～ 0.00002 × CI) and Re/Os ratios that were modestly elevated (187Re/188Os = 0.6 to 1.7) relative to CI chondrites. MGS samples are, on average, characterised by more elevated HSE abundances (～ 0.00007 × CI) compared with FAN. This either reflects contrasting mantle-source HSE characteristics of FAN and MGS rocks, or different mantle–crust HSE fractionation behaviour during production of these lithologies. Previous studies of lunar impact-melt rocks have identified possible elevated Ru and Pd in lunar crustal target rocks. The new results provide no supporting evidence for such enrichments.If maximum estimates for HSE in the lunar mantle are compared with FAN and MGS averages, crust–mantle concentration ratios (D-values) must be ≤ 0.3. Such D-values are broadly similar to those estimated for partitioning between the terrestrial crust and upper mantle, with the notable exception of Re. Given the presumably completely different mode of origin for the primary lunar floatation crust and tertiary terrestrial continental crust, the potential similarities in crust–mantle HSE partitioning for the Earth and Moon are somewhat surprising. Low HSE abundances in the lunar crust, coupled with estimates of HSE concentrations in the lunar mantle implies there may be a ‘missing component’ of late-accreted materials (as much as 95%) to the Moon if the Earth/Moon mass-flux estimates are correct and terrestrial mantle HSE abundances were established by late accretion.  相似文献   

13.
Energy dispersive spectrometry (EDS), laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) track analyses of chlorite-dominated quench-textured microkrystite spherules and LA-ICPMS spot analyses of intra-spherule Ni-rich skeletal quench chromites from the 3243 ± 4 Ma Barberton S3 impact fallout unit (lower part of the Mapepe Formation, Fig Tree Group, Barberton greenstone belt, Kaapvaal Craton, South Africa) reveal fractionated siderophile and PGE trace element patterns corresponding to chondrite-contaminated komatiite/basalt compositions. The chlorites, interpreted as altered glass, contain sharp siderophile elements and PGE spikes inherited from decomposed metal and Ni-rich chromite particles. LA-ICPMS spot analysis identifies PGE-rich micronuggets in Ni–chromites (Ir ∼ 12–100 ppm, Os ∼ 9–86 ppm, Ru ∼ 5–43 ppm) and lower levels of the volatile PGEs (Rh ∼ 1–11 ppm, Pd ∼ 0.68–0.96 ppm). Previously reported PGE anomalies in the order of hundreds of ppb in some Barberton microkrystite spherules are accounted for in terms of disintegration of PGE-rich micronuggets. Replacement of the Ni-chromites by sulphide masks primary chondritic patterns and condensation element distribution effects. High refractory/volatile PGE ratios pertain to both the chlorites and the Ni-rich chromites, consistent with similar compositional relations in microkrystite spherules from other impact fallout units in the Barberton greenstone belt and the Pilbara Craton, Western Australia. The near-consistent low Pt/Re and high V/Cr and V/Sc ratios in chlorite of the spherules, relative to komatiites, are suggestive of selective atmospheric condensation of the spherules which favored the relatively more refractory Re and V. Selective condensation may also be supported by depletion in the volatile Yb relative to Sm. Ni–Cr relationships allow estimates of the proportion of precursor crustal and meteoritic components of the spherules. Mass balance calculations based on the iridium flux allow estimates of the order of magnitude of the diameter of the chondritic projectile.  相似文献   

14.
We report new high-precision laser fluorination three-isotope oxygen data for lunar materials. Terrestrial silicates with a range of δ18O values (− 0.5 to 22.9‰) were analyzed to independently determine the slope of the terrestrial fractionation line (TFL; λ = 0.5259 ± 0.0008; 95% confidence level). This new TFL determination allows direct comparison of lunar oxygen isotope systematics with those of Earth. Values of Δ17O for Apollo 12, 15, and 17 basalts and Luna 24 soil samples average 0.01‰ and are indistinguishable from the TFL. The δ18O values of high- and low-Ti lunar basalts are distinct. Average whole-rock δ18O values for low-Ti lunar basalts from the Apollo 12 (5.72 ± 0.06‰) and Apollo 15 landing sites (5.65 ± 0.12‰) are identical within error and are markedly higher than Apollo 17 high-Ti basalts (5.46 ± 0.11‰). Evolved low-Ti LaPaz mare-basalt meteorite δ18O values (5.67 ± 0.05‰) are in close agreement with more primitive low-Ti Apollo 12 and 15 mare basalts. Modeling of lunar mare-basalt source composition indicates that the high- and low-Ti mare-basalt mantle reservoirs were in oxygen isotope equilibrium and that variations in δ18O do not result from fractional crystallization. Instead, these differences are consistent with mineralogically heterogeneous mantle sources for mare basalts, and with lunar magma ocean differentiation models that result in a thick feldspathic crust, an olivine–pyroxene-rich mantle, and late-stage ilmenite-rich zones that were convectively mixed into deeper portions of the lunar mantle. Higher average δ18O (WR) values of low-Ti basalts compared to terrestrial mid ocean ridge basalts (Δ=0.18‰) suggest a possible oxygen isotopic difference between the terrestrial and lunar mantles. However, calculations of the δ18O of lunar mantle olivine in this study are only 0.05‰ higher than terrestrial mantle olivine. These observations may have important implications for understanding the formation of the Earth–Moon system.  相似文献   

15.
Miocene to Quaternary large basaltic plateaus occur in the back-arc domain of the Andean chain in Patagonia. They are thought to result from the ascent of subslab asthenospheric magmas through slab windows generated from subducted segments of the South Chile Ridge (SCR). We have investigated three volcanic centres from the Lago General Carrera–Buenos Aires area (46–47°S) located above the inferred position of the slab window corresponding to a segment subducted 6 Ma ago. (1) The Quaternary Río Murta transitional basalts display major, trace elements, and Sr and Nd isotopic features similar to those of oceanic basalts from the SCR and from the Chile Triple Junction near Taitao Peninsula (e.g., (87Sr/86Sr)o = 0.70396–0.70346 and εNd = + 5.5 − + 3.0). We consider them as derived from the melting of a Chile Ridge asthenospheric mantle source containing a weak subduction component. (2) The Plio-Quaternary (< 3.3 Ma) post-plateau basanites from Meseta del Lago Buenos Aires (MLBA), Argentina, likely derive from small degrees of melting of OIB-type mantle sources involving the subslab asthenosphere and the enriched subcontinental lithospheric mantle. (3) The main plateau basaltic volcanism in this region is represented by the 12.4–3.3-Ma-old MLBA basalts and the 8.2–4.4-Ma-old basalts from Meseta Chile Chico (MCC), Chile. Two groups can be distinguished among these main plateau basalts. The first group includes alkali basalts and trachybasalts displaying typical OIB signatures and thought to derive from predominantly asthenospheric mantle sources similar to those of the post-plateau MLBA basalts, but through slightly larger degrees of melting. The second one, although still dominantly alkalic, displays incompatible element signatures intermediate between those of OIB and arc magmas (e.g., La/Nb > 1 and TiO2 < 2 wt.%). These intermediate basalts differ from their strictly alkalic equivalents by having lower High Field Strength Element (HFSE) and higher εNd (up to + 5.4). These features are consistent with their derivation from an enriched mantle source contaminated by ca. 10% rutile-bearing restite of altered oceanic crust. The petrogenesis of the studied Mio-Pliocene basalts from MLBA and MCC is consistent with contributions of the subslab asthenosphere, the South American subcontinental lithospheric mantle and the subducted Pacific oceanic crust to their sources. However, their chronology of emplacement is not consistent with an ascent through an asthenospheric window opened as a consequence of the subduction of segment SCR-1, which entered the trench at 6 Ma. Indeed, magmatic activity was already important between 12 and 8 Ma in MLBA and MCC as well as in southernmost plateaus, i.e., 6 Ma before the subduction of the SCR-1 segment. We propose a geodynamic model in which OIB and intermediate magmas derived from deep subslab asthenospheric mantle did uprise through a tear-in-the-slab, which formed when the southernmost segments of the SCR collided with the Chile Trench around 15 Ma. During their ascent, they interacted with the Patagonian supraslab mantle and, locally, with slivers of subducted Pacific oceanic crust that contributed to the geochemical signature of the intermediate basalts.  相似文献   

16.
The aggregate shear wave velocities of MgO (periclase) have been determined throughout Earth's lower mantle pressure regime approaching 130 GPa using Brillouin spectroscopy in conjunction with synchrotron X-ray diffraction technique in a diamond anvil cell apparatus. We found that the extrapolations of the high-pressure shear wave velocities and shear moduli to ambient pressure are highly consistent with earlier studies. However, the measurements over a wide pressure range revealed that the pressure derivative of the shear modulus (dG/dP = G0′) of MgO is 1.92(2), which is distinctly lower than that of previous lower-pressure experiments. Compared with the previous results on (Mg,Fe)O ferropericlase, there is no clear correlation between iron content and G0′. We calculate that the shear wave velocity profile of lower mantle along the adiabatic geotherm applied by the lower G0′ value of periclase can remarkably well reproduce the global seismological 1-D velocity profile model with uniform composition model. The best-fitting result indicates the possibility of a lower mantle mineralogy with ~ 92 vol.% silicate perovskite phase, implying that the bulk composition of lower mantle is likely not to be pyrolitic but more chondritic. The present acoustic measurements performed over the large pressure range have thus led us to a better understanding of compositional model of the Earth's lower mantle.  相似文献   

17.
High precision Mg isotope measurements by multi-collector ion microprobe show that refractory olivines from the Allende chondrite, either olivines isolated in the matrix (2 samples studied) or olivines in type I chondrules (6 samples studied), have variable δ26Mg* enrichments and deficits (calculated in permil as the 26Mg deviation from the instrumental mass fractionation line) relative to the Earth. Most average δ26Mg* (noted δ26Mg*av) values (between 10 and 20 analyses per chondrule) are negative but the total range is from ?0.029 (± 0.010) ‰ (2 sigma errors) to + 0.011 (± 0.011) ‰ with an exception of one olivine at + 0.043 (± 0.023) ‰. These variations in δ26Mg*av reflect the formation of the olivines from reservoirs enriched in various amounts of 26Mg by the decay of short-lived 26Al (T1/2 = 0.73 Ma). Similarly, 30 analyses of olivines from the Eagle Station pallasite show a δ26Mg*av value of ?0.033 ± 0.008‰, as negative as some olivines from Allende chondrules and the Solar system initial δ26Mg* value of ?0.038 ± 0.004‰ (defined at the time of formation of type B Ca–Al-rich inclusions – CAIs – when 26Al/27Al = 5.23 × 10?5, Jacobsen et al., 2008).Because olivines are Al-poor and because their Mg isotopic compositions are not reset during the chondrule forming events, their δ26Mg*av can be used to calculate model crystallization ages relative to various theoretical Mg isotope growth curves. The two end-member scenarios considered are (i) a “nebular” growth in which the Al/Mg ratio remains chondritic and (ii) a “planetary” growth in which a significant increase of the Al/Mg ratio can be due to, for instance, olivine magmatic fractionation. The low δ26Mg*av value of olivines from the Eagle Station pallasite demonstrate that metal-silicate differentiation occurred as early as ~ 0. 15- 0. 23+ 0. 29 Ma after CAIs in either of the growth scenarios. Similarly the variable δ26Mg*av values of refractory olivines can be understood if they were formed in planetesimals which started to differentiate as early as the Eagle Station parent body. Accretion of these planetesimals must have been coeval to the formation of CAIs and their disruption could explain why their fragments (Mg-rich olivines) were distributed in the chondrule forming regions of the disk.  相似文献   

18.
A model of core formation is presented that involves the Earth accreting heterogeneously through a series of impacts with smaller differentiated bodies. Each collision results in the impactor's metallic core reacting with a magma ocean before merging with the Earth's proto-core. The bulk compositions of accreting planetesimals are represented by average solar system abundances of non-volatile elements (i.e. CI-chondritic), with 22% enhancement of refractory elements and oxygen contents that are defined mainly by the Fe metal/FeO silicate ratio. Based on an anhydrous bulk chemistry, the compositions of coexisting core-forming metallic liquid and peridotitic silicate liquid are calculated by mass balance using experimentally-determined metal/silicate partition coefficients for the elements Fe, Si, O, Ni, Co, W, Nb, V, Ta and Cr. Oxygen fugacity is fixed by the partitioning of Fe between metal and silicate and depends on temperature, pressure and the oxygen content of the starting composition. Model parameters are determined by fitting the calculated mantle composition to the primitive mantle composition using least squares minimization. Models that involve homogeneous accretion or single-stage core formation do not provide acceptable fits. In the most successful models, involving 24 impacting bodies, the initial 60–70% (by mass) of the Earth accretes from highly-reduced material with the final 30–40% of accreted mass being more oxidised, which is consistent with results of dynamical accretion simulations. In order to obtain satisfactory fits for Ni, Co and W, it is required that the larger (and later) impactor cores fail to equilibrate completely before merging with the Earth's proto-core, as proposed previously on the basis of Hf-W isotopic studies. Estimated equilibration conditions may be consistent with magma oceans extending to the core–mantle boundary, thus making core formation extremely efficient. The model enables the compositional evolution of the Earth's mantle and core to be predicted throughout the course of accretion. The results are consistent with the late accretion of the Earth's water inventory, possibly with a late veneer after core formation was complete. Finally, the core is predicted to contain ~ 5 wt.% Ni, ~ 8 wt.% Si, ~ 2 wt.% S and ~ 0.5 wt.% O.  相似文献   

19.
New measurements of mass-dependent calcium isotope effects in meteorites, lunar and terrestrial samples show that Earth, Moon, Mars, and differentiated asteroids (e.g., 4-Vesta and the angrite and aubrite parent bodies) are indistinguishable from primitive ordinary chondritic meteorites at our current analytical resolution (± 0.07‰ SD for the 44Ca/40Ca ratio). In contrast, enstatite chondritic meteorites are slightly enriched in heavier calcium isotopes (ca. + 0.5‰) and primitive carbonaceous chondritic meteorites are depleted in heavier calcium isotopes (ca. ? 0.5‰). The calcium isotope effects cannot be easily ascribed to evaporation or intraplanetary differentiation processes. The isotopic variations probably survive from the earliest stages of nebular condensation, and indicate that condensation occurred under non-equilibrium (undercooled nebular gas) conditions. Some of this early high-temperature calcium isotope heterogeneity is recorded by refractory inclusions (Niederer and Papanastassiou, 1984) and survived in planetesimals, but virtually none of it survived through terrestrial planet accretion. The new calcium isotope data suggest that ordinary chondrites are representative of the bulk of the refractory materials that formed the terrestrial planets; enstatite and carbonaceous chondrites are not. The enrichment of light calcium isotopes in bulk carbonaceous chondrites implies that their compositions are not fully representative of the solar nebula condensable fraction.  相似文献   

20.
In an attempt to quantify the extent of geochemical heterogeneity within a restricted and well dated portion of the upper mantle, 27 chromite separates from the 90 My old chromite deposits in the Mayarí–Baracoa ophiolite belt in eastern Cuba have been investigated for platinum group element (PGE) concentrations and Re–Os isotopic systematics. The samples are characterized by systematically subchondritic initial 187Os/188Os ratios and substantial heterogeneity. The initial 187Os/188Os ratios vary with chromite chemistry and with geographical distribution, reflecting differences in the Os isotopic evolution for the different upper mantle sections represented by the ophiolite. Accordingly, the Os isotope data might be divided into three groups. In the Moa–Baracoa district, where the chromite bodies are located in the mantle–crust transition zone, the calculated initial γOs values average − 0.97 ± 0.69 (n = 13). In the Sagua de Tanamo district, where chromite chemistry is highly variable and their location in relation the mantle sequence is less clear, the initial γOs values are intermediate, with an average of − 1.77 ± 0.80 (n = 7). In the Mayarí district, where the chromite bodies are located in the lower part of the mantle sequence, initial γOs values average − 2.66 ± 0.29 (n = 7). These subchondritic (i.e. negative) initial γOs values are most simply explained by Re depletion during ancient partial melting and/or melt percolation events.The Os isotope heterogeneity documented here indicates a high degree of geochemical complexity on small to intermediate length scales in the upper mantle. Our results, in combination with data on chromites from the literature, show that an “average present-day Os isotopic composition” for the hypothetical depleted MORB mantle (DMM) reservoir cannot be precisely established beyond the statement that it is “broadly chondritic”. Indeed, the upper mantle cannot be considered a sufficiently homogeneous geochemical “reservoir” to serve meaningfully as a baseline against which geochemical “anomalies” are evaluated. On the other hand, our findings are consistent with the “Statistical Upper Mantle Assemblage” or “SUMA”-concept, according to which a high level of geochemical heterogeneity is maintained in the upper mantle at all relevant length scales, as a result of the plate-tectonic cycle and intra-mantle processes such as melt-migration and metasomatism.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号