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1.
Lithium isotope fractionation in the southern Cascadia subduction zone   总被引：2，自引：0，他引：2  
We present lithium (Li) abundances and isotope compositions for a suite of anhydrous olivine tholeiites (HAOTs) and hydrous basalt-andesitic (BA) lavas from the Mt. Shasta and Medicine Lake regions, California. The values of δ7Li vary from + 0.9‰ to + 6.4‰ and correlate inversely with distance from the trench. These data are consistent with continuous isotope fractionation of Li during dehydration of the subducted oceanic lithosphere, an interpretation corroborated by uniformly high pre-eruptive H2O contents in basaltic andesites accompanied by high Li, Rb, Sr, Ba and Pb abundances. The subduction-derived component that was added to these hydrous magmas is shown to be very similar beneath both Mt. Shasta and Medicine Lake volcanoes despite characteristically distinct Li isotope compositions in the magmas themselves. More evolved andesites and dacites from Mt. Shasta have δ7Li from + 2.8 to + 6.9‰ which is identical with the range obtained for HAOTs and BA lavas from Mt. Shasta. Therefore, Li isotopes do not provide evidence for any other crustal component admixed to Mt. Shasta andesites or dacites during magmatic differentiation and magma mixing in the crust.  相似文献   

2.
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   

3.
High-precision in-situ ion microprobe (SIMS) oxygen isotope analysis of zircons from two diorite intrusions associated with the late Caledonian Lochnagar pluton in Scotland has revealed large differences in the degree of heterogeneity in zircon δ18O between the diorites. Zircon crystals from the Cul nan Gad diorite (CnG) show a unimodal distribution of oxygen isotope values (δ18O = 6.0 ± 0.6‰ (2σ)) and no or only minor grain-scale variation. Those from the Allt Darrarie diorite (AD1) show a large range in δ18O and an apparent bimodal distribution with modes of 6.6 ± 0.4‰ and 7.3 ± 0.4‰. Variations of up to 1.2‰ occur between and within grains; both an increase and decrease in δ18O with zircon growth has been observed. The δ18O composition of growing zircon can only change if open-system processes affect the magma composition, i.e. if material of contrasting δ18O composition is added to the magma. The variability in AD1 is interpreted to represent a cryptic record of magma mixing. A ‘deep crustal hot zone’ is a likely site for generation of the dioritic magmas which developed by mixing of residual melts and crustal partial melts or by melting of mafic lower crustal rocks. The overall small number of zircons with mantle-like δ18O values (5.3 ± 0.6‰ (2σ)) in the Lochnagar diorites is largely the product of crustal differentiation rather than crustal growth.

The δ18O of quartz from the CnG and AD1 diorites shows only minor variation (CnG: 10.9 ± 0.5‰ (2σ), AD1: 11.7 ± 0.6‰ (2σ)) within single populations, with no evidence of mixing. Quartz–zircon isotopic disequilibrium is consistent with later crystallisation of quartz from late magmatic fluids, and in case of the AD1 diorite after the inferred magma mixing from a homogenised, higher δ18O melt.

High-precision SIMS oxygen isotope analysis of zircon provides a new approach to identifying and resolving previously undetected early-stage magma mixing and constraining the compositions and origins of the component magmas. A combination of zircon, quartz and whole-rock data has proven to be a powerful tool in reconstructing the petrogenetic evolution of diorite from early crystallisation to late alteration.  相似文献   


4.
Zinc stable isotopes in seafloor hydrothermal vent fluids and chimneys   总被引：3，自引：0，他引：3  
Many of the heaviest and lightest natural zinc (Zn) isotope ratios have been discovered in hydrothermal ore deposits. However, the processes responsible for fractionating Zn isotopes in hydrothermal systems are poorly understood. In order to better assess the total range of Zn isotopes in hydrothermal systems and to understand the factors which are responsible for this isotopic fractionation, we have measured Zn isotopes in seafloor hydrothermal fluids from numerous vents at 9–10°N and 21°N on the East Pacific Rise (EPR), the TAG hydrothermal field on the Mid-Atlantic Ridge, and in the Guaymas Basin. Fluid δ66Zn values measured at these sites range from + 0.00‰ to + 1.04‰. Of the many physical and chemical parameters examined, only temperature was found to correlate with fluid δ66Zn values. Lower temperature fluids (< 250 °C) had both heavier and more variable δ66Zn values compared to higher temperature fluids from the same hydrothermal fields. We suggest that subsurface cooling of hydrothermal fluids leads to precipitation of isotopically light sphalerite (Zn sulfide), and that this process is a primary cause of Zn isotope variation in hydrothermal fluids. Thermodynamic calculations carried out to determine saturation state of sphalerite in the vent fluids support this hypothesis with isotopically heaviest Zn found in fluids that were calculated to be saturated with respect to sphalerite. We have also measured Zn isotopes in chimney sulfides recovered from a high-temperature (383 °C) and a low-temperature (203 °C) vent at 9–10°N on the EPR and, in both cases, found that the δ66Zn of chimney minerals was lighter or similar to the fluid δ66Zn. The first measurements of Zn isotopes in hydrothermal fluids have revealed large variations in hydrothermal fluid δ66Zn, and suggest that subsurface Zn sulfide precipitation is a primary factor in causing variations in fluid δ66Zn. By understanding how chemical processes that occur beneath the seafloor affect hydrothermal fluid δ66Zn, Zn isotopes may be used as a tracer for studying hydrothermal processes.  相似文献   

5.
Nitrogen contents range from a few parts per million in ordinary chondrites and achondrites to several hundred parts per million in enstatite chondrites and carbonaceous chondrites. Four major isotopic groups are recognized: (1) C1 and C2 carbonaceous chondrites have δ15N of+30to+50%.; (2) enstatite chondrites have δ15N of?30to?40‰; (3) C3 chondrites have low δ15N with large internal variations; (4) ordinary chondrites have δ15N of?10to+20‰. The major variations are primary, representing isotopic abundances established at the time of condensation and accretion. Secondary processes, such as spallation reactions, solar wind implantation and metamorphic loss may cause small but observable isotopic variations in particular cases. The large isotopic difference between enstatite chondrites and carbonaceous chondrites cannot be accounted for by equilibrium condensation from a homogeneous nebular gas, and requires either unusually large kinetic effects, or a temporal or spatial variation of isotopic composition of the nebula. Nitrogen isotopic heterogeneity in the nebula due to nuclear processes has not been firmly established, but may be required to account for the large variations found within the Allende and Leoville meteorites. The unique carbonaceous chondrite, Renazzo, has δ15N of+170%., which is well beyond the range of all other data, and also requires a special source. It is not yet possible, from the meteoritic data, to establish the mode of accretion of nitrogen onto the primitive Earth.  相似文献   

6.
The stable isotopic composition of hydrogen and oxygen (δ2H and δ18O) and tritium activity (3H) were monitored in monthly precipitation at two continental stations (Ljubljana, Zagreb) and six stations along the eastern Adriatic coasts of Slovenia and Croatia in the period 2001–2003. Mean air temperatures and amount of precipitation were also recorded.

Distinct differences in both meteorological and isotopic data between the continental and maritime stations were observed. Seasonal variations in δ18O are smaller at the maritime stations than at the continental ones due to smaller seasonal temperature variations. A good correlation between δ18O and δ2H was obtained for each station, and the local meteoric water lines are close to the Global Meteoric Water Line, with a decreasing trend of slope for the south-Adriatic stations. Good correlations between δ18O in monthly precipitation and mean monthly air temperature were observed at all stations. The slope of δ18O vs. T varied between 0.37‰ °C−1 and 0.15‰ °C−1. Mean 3H activity and seasonal variation of 3H activity are smaller at maritime stations than at continental ones. Additionally, 3H activity decreases in the NW–SE direction of the Adriatic coast.

The study of spatial variations over this relatively small area rich in geographical and climatic diversities showed the complexity of the isotopic composition of precipitation and the isotopic data obtained for eight stations, most of them in the karstic area along the Adriatic coast, and gave valuable information for regional hydrological investigations and modelling of isotope variability over the Mediterranean basin.  相似文献   


7.
Nitrogen isotope fractionations have been measured in Fischer-Tropsch and Miller-Urey reactions in order to determine whether these processes can account for the large15N/14N ratios found in organic matter in carbonaceous chondrites. Polymeric material formed in the Fischer-Tropsch reaction was enriched in15N by only 3‰ relative to the starting material (NH3). The15N enrichment in polymers from the Miller-Urey reaction was 10–12‰. Both of these fractionations are small compared to the 80–90‰ differences observed between enstatite chondrites and carbonaceous chondrites. These large differences are apparently due to temporal or spatial variations in the isotopic composition of nitrogen in the solar nebula, rather than to fractionation during the production of organic compounds.  相似文献   

8.
58 samples of fossil mammoth and reindeer teeth and bones of various ages and coming from different locations were studied for the oxygen isotopic composition of their phosphate. Samples from Siberia have interstadial (Marine Isotope Stage 3), stadial (MIS 2), late-glacial and post-glacial ages. Russian and Ukrainian samples refer to the late-glacial and transitional (between the interstadial and glacial stages) time. The δ18O of palaeoenvironmental waters were calculated from the δ18Op obtained from fossil samples by means of the isotope equations calibrated on modern specimens of elephants and deer respectively. The δ18Ow obtained are generally lighter than those measured nowadays in the same areas and not far from those measured on ice cores of Holocene age, the isotopic differences being not greater than a few δ units. The calculated values are also in fairly good agreement with some isotopic values obtained from Siberian permafrost samples. According to the results obtained it seems that the elephant and deer equations can be reasonably used respectively in the case of fossil mammoth and deer skeletons to evaluate environmental palaeowaters.  相似文献   

9.
In order to understand the origin of iron-rich olivine in the matrices of type 3 ordinary chondrites, the reaction of metallic iron and enstatite, with and without forsterite and SiO2, has been experimentally reproduced at temperatures between 1150° and 800°C and PO2 between 10−11 and 10−16 atm (between the IQF and MW buffers). The olivine produced ranges from Fo58 to Fo34 and this composition does not change significantly with temperature and time of the runs. The magnesian olivine which forms does become more magnesian with increasing forsterite/enstatite ratio of the starting materials. Iron-rich olivine (Fo< 35) cannot be formed by the reaction of enstatite and metallic iron, with or without forsterite as starting materials but it can be formed in the presence of free silica. The composition of olivine becomes more iron-rich with increasing silica/enstatite ratio. The compositional range of olivine formed from each mixture is 25–30 mole% Fo regardless of the temperature, composition, mineral assemblage, and run duration.From these experimental results, two possibilities suggested for the origin of the iron-rich olivine in the matrices of type 3 ordinary chondrites: (1) free silica must have been present if the iron-rich olivine was formed by solid-state reactions under oxidizing condition in the solar nebula; (2) reaction of silicon-rich gas with metallic iron took place under oxidizing condition in the solar nebula. Though it is difficult to define which alternative was dominant, the formation of free silica or silicon-rich gas may be a result of fractional condensation. This is possible if there is a reaction relation between forsterite and gas to produce enstatite. The suggested fractional condensation is supported by the fact that the compositions of the fine-grained matrices of type 3 ordinary chondrites are more silica-rich than the bulk compositions of the chondrites. Though it is not known whether such conditions were established all over the nebula or locally in the nebula, both fractionation and more oxidizing conditions than the average solar nebula are required for the formation of matrix olivine.  相似文献   

10.
The response of a climate proxy against measured temperature, rainfall and atmospheric circulation patterns at sub-annual resolution is the ultimate test of proxy fidelity but very few data exist showing the level of correspondence between speleothem climate proxies and the instrumental climate record. Cave sites on the Gibraltar peninsula provide a unique opportunity to calibrate speleothem climate proxies with the longest known available precipitation isotopes and instrumental records. An actively growing speleothem sampled from New St. Michaels Cave in 2004 is composed of paired laminae consisting of light columnar calcite and a darker microsparitic calcite. Stable isotope analysis of samples micromilled in 100 μm steps at the equivalent of bi-monthly intervals reveals fabric-correlated annual cycles in carbon isotopes, oxygen isotopes and trace elements responding to seasonal changes in cave microclimate, hydrology and ventilation patterns. Calcite δ13C values reach a minimum in the light columnar fabric and evidence from trace element behaviour and cave monitoring indicates that this grows under cave ‘winter’ conditions of highest pCO2, whereas the dark microsparitic calcite, characterised by elevated δ13C and δ18O values grows under low ‘summer’ pCO2 conditions. Drip water δ13CDIC reaches a minimum in March–April, at which time the attenuated δ18O signal becomes most representative of winter precipitation. An age model based on cycle counting and the position of the 14C bomb carbon spike yields a precisely dated winter oxygen isotope proxy of cave seepage water for comparison with the GNIP and instrumental climate record for Gibraltar. The δ18O characteristics of calcite deposited from drip water representing winter precipitation for each year can be derived from the seasonally resolved record and allows reconstruction of the δ18O drip water representing winter precipitation for each year from 1951–2004. These data show an encouraging level of correspondence (r2 = 0.47) with the δ18O of rainfall falling each year between October and March and on a decadal scale the δ18O of reconstructed winter drip water mirrors secular change in mean winter temperatures.  相似文献   

11.
On the basis of18O/16O and17O/16O ratios, meteorites and planets can be grouped into at least six categories, as follows: (1) the terrestrial group, consisting of the earth, moon, differentiated meteorites and enstatite chondrites; (2) types L and LL ordinary chondrites; (3) type H ordinary chondrites; (4) anhydrous minerals of C2, C3, C4 carbonaceous chondrites; (5) hydrous matrix minerals of C2 carbonaceous chondrites; (6) the ureilites. Objects of one category cannot be derived by fractionation or differentiation from the source materials of any other category.  相似文献   

12.
Isotopic anomalies in Mo and Zr have recently been reported for bulk chondrites and iron meteorites and have been interpreted in terms of a primordial nucleosynthetic heterogeneity in the solar nebula. We report precise Zr isotopic measurements of carbonaceous, ordinary and enstatite chondrites, eucrites, mesosiderites and lunar rocks. All bulk rock samples yield isotopic compositions that are identical to the terrestrial standard within the analytical uncertainty. No anomalies in 92Zr are found in any samples including high Nb/Zr eucrites and high and low Nb/Zr calcium-aluminum-rich inclusions (CAIs). These data are consistent with the most recent estimates of <10−4 for the initial 92Nb/93Nb of the solar system. There exists a trace of isotopic heterogeneity in the form of a small excess of r-process 96Zr in some refractory CAIs and some metal-rich phases of Renazzo. A more striking enrichment in 96Zr is found in acetic acid leachates of the Allende CV carbonaceous chondrite. These data indicate that the r- and s-process Zr components found in presolar grains were well mixed on a large scale prior to planetary accretion. However, some CAIs formed before mixing was complete, such that they were able to sample a population of r-process-enriched material. The maximum amount of additional r-process component that was added to the otherwise well-mixed Zr in the molecular cloud or disk corresponds to ∼0.01%.  相似文献   

13.
Stable isotope values of Costa Rican surface waters   总被引：3，自引：0，他引：3  
Stable isotope data of surface waters from the humid tropics in general, and Costa Rica in particular, are scarce. To improve our understanding of the spatial distribution of stable isotopes in surface waters, we measured δ18O and δD in river and lake (n=63) and precipitation (n=3) samples from Costa Rica. We also present data from the IAEA/WMO isotopes in precipitation network as context for our study. Surface water isotope values do not strongly correlate with elevation, stream head elevation, stream length, distance from Caribbean Sea, or estimated mean annual precipitation for the country as a whole. However, the data show distinct regional trends. The δ18O and δD values downwind of mountain ranges are inversely related to the altitude of the ranges the air masses traverse. In the lee of the high Talamanca Range, δ18O values are 6–8‰ lower, while in the lee of the lower Tilarán Range δ18O values are 2–3‰ lower than upwind sites along the Caribbean Slope. An altitude effect of −1.4‰ δ18O/km is present on the Pacific slope of southern Costa Rica, equivalent to a temperature effect of −0.3‰/°C. The Nicoya and Osa Peninsulas have higher values than upwind sites, suggesting input of Pacific-sourced moisture, evaporative enrichment, or decreased condensation temperatures. Elevated and increasing d-excess values inland along the Nicaragua Trough suggest a recycled component may be an important contributor to the water budget. These data provide preliminary stable isotope information for Costa Rica, and will benefit paleoclimatic research in the region. More detailed studies would be beneficial to our understanding of the controls on stable isotope composition of tropical waters.  相似文献   

14.
We have discovered four clasts in three ordinary-chondrite regolith breccias which are a new kind of type 3 chondrite. Like ordinary and carbonaceous type 3 chondrites, they have distinct chondrules, some of which contain glass, highly heterogeneous olivines and pyroxenes, and predominantly monoclinic low-Ca pyroxenes. But instead of the usual fine-grained, Fe-rich silicate matrix, the clasts have a matrix composed largely of aggregates of micron- and submicron-sized graphite and magnetite. The bulk compositions of the clasts as well as the types of chondrules (largely porphyritic) are typical of type 3 ordinary chondrites, although chondrules in the clasts are somewhat smaller (0.1–0.5 mm). A close relationship with ordinary chondrites is also indicated by the presence of similar graphite-magnetite aggregates in seven type 3 ordinary chondrites. This new kind of chondrite is probably the source of the abundant graphite-magnetite inclusions in ordinary-chondrite regolith breccias, and may be more common than indicated by the absence of whole meteorites made of chondrules and graphite-magnetite.  相似文献   

15.
Negative carbon-isotope excursions have been comprehensively studied in the stratigraphic record but the discussion of causal mechanisms has largely overlooked the potential role of biomass burning. The carbon-isotopic ratios (δ13C) of vegetation, soil organic matter and peat are significantly lower than atmospheric carbon dioxide (CO2), and thereby provide a source of low 13C CO2 when combusted. In this study, the potential role of biomass burning to generate negative carbon isotope excursions associated with greenhouse climates is modeled. Results indicate that major peat combustion sustained for 1000 yr increases atmospheric CO2 from 2.5× present atmospheric levels (PAL) to 4.6× PAL, and yields a pronounced negative δ13C excursion in the atmosphere ( 2.4‰), vegetation ( 2.4‰) and the surface ocean ( 1.2‰), but not for the deep ocean ( 0.9‰). Release of CO2 initiates a short-term warming of the atmosphere (up to 14.4 °C, with a duration of 1628 yr), which is consistent with the magnitude and length of an observed Toarcian excursion event. These results indicate that peat combustion is a plausible mechanism for driving negative δ13C excursions in the rock record, even during times of elevated pCO2.  相似文献   

16.
Isotopic variations in melting snow are poorly understood. We made weekly measurements at the Central Sierra Snow Laboratory, California, of snow temperature, density, water equivalent and liquid water volume to examine how physical changes within the snowpack govern meltwater δ18O. Snowpack samples were extracted at 0.1 m intervals from ground level to the top of the snowpack profile between December 1991 and April 1992. Approximately 800 mm of precipitation fell during the study period with δ18O values between −21.35 and −4.25‰. Corresponding snowpack δ18O ranged from −22.25 to −6.25‰. The coefficient of variation of δ18O in snowpack levels decreased from −0.37 to −0.07 from winter to spring, indicating isotopic snowpack homogenization. Meltwater δ18O ranged from −15.30 to −8.05‰, with variations of up to 2.95‰ observed within a single snowmelt episode, highlighting the need for frequent sampling. Early snowmelt originated in the lower snowpack with higher δ18O through ground heat flux and rainfall. After the snowpack became isothermal, infiltrating snowmelt displaced the higher δ18O liquid in the lower snowpack through a piston flow process. Fractionation analysis using a two-component mixing model on the isothermal snowpack indicated that δ18O in the initial and final half of major snowmelt was 1.30‰ lower and 1.45‰ higher, respectively, than the value from simple mixing. Mean snowpack δ18O on individual profiling days showed a steady increase from −15.15 to −12.05‰ due to removal of lower δ18O snowmelt and addition of higher δ18O rainfall. Results suggest that direct sampling of snowmelt and snow cores should be undertaken to quantify tracer input compositions adequately. The snowmelt sequence also suggests that regimes of early lower δ18O and later higher δ18O melt may be modeled and used in catchment tracing studies.  相似文献   

17.
The main group pallasites and the mesosiderites fall within the oxygen isotope group previously determined for the calcium-rich achondrites (eucrites, howardites and diogenites), consistent with derivation from a common source material, and perhaps a common parent body. The group IIE iron meteorites were derived from the same source material as H-group ordinary chondrites. The chondrite-like silicate inclusions in group IAB iron meteorites are not related to the ordinary chondrites, but may be related to the enstatite chondrites. Several meteorites previously considered “anomalous” fall into these groups: Pontlyfni and Winona with the IAB irons, and Netschaëvo possibly with the H chondrites and IIE irons. The unusual pallasites Eagle Station and Itzawisis have remarkable oxygen isotopic compositions, and have more of the 16O-rich component than any other meteorite. Bencubbin and Weatherford are also unusual in their isotopic compositions, and may bear some relationship to the C2 carbonaceous chondrites. Lodran and Enon are isotopically similar to one another and are close to the achondrite-mesosiderite-pallasite group.  相似文献   

18.
Computer aided multi-parameter signal correlation is used to develop a common high-precision age model for eight gravity cores from the subtropical and subantarctic South Atlantic. Since correlations between all pairs of multi-parameter sequences are used, and correlation errors between core pairs (A, B) and (B, C) are controlled by comparison with (A, C), the resulting age model is called a stratigraphic network. Precise inter-core correlation is achieved using high-resolution records of magnetic susceptibility κ, wet bulk density ρ and X-ray fluorescence scans of elemental composition. Additional δ18O records are available for two cores. The data indicate nearly undisturbed sediment series and the absence of significant hiatuses or turbidites. After establishing a high-precision common depth scale by synchronously correlating four densely measured parameters (Fe, Ca, κ, ρ), the final age model is obtained by simultaneously fitting the aligned δ18O and κ records of the stratigraphic network to orbitally tuned oxygen isotope [J. Imbrie, J. D. Hays, D. G. Martinson, A. McIntyre, A. C. Mix, J. J. Morley, N. G. Pisias, W. L. Prell, N. J. Shackleton, The orbital theory of Pleistocene climate: support from a revised chronology of the marine δ18O record, in: A. Berger, J. Imbrie, J. Hays, G. Kukla, B. Saltzman (Eds.), Milankovitch and Climate: Understanding the Response to Orbital Forcing, Reidel Publishing, Dordrecht, 1984, pp. 269-305; D. Martinson, N. Pisias, J. Hays, J. Imbrie, T. C. Moore Jr., N. Shackleton, Age dating and the orbital theory of the Ice Ages: development of a high-resolution 0 to 300.000-Year chronostratigraphy, Quat. Res. 27 (1987) 1-29.] or susceptibility stacks [T. von Dobeneck, F.Schmieder, Using rock magnetic proxy records for orbital tuning and extended time series analyses into the super-and sub-Milankovitch Bands, in: G. Fischer, G. Wefer (Eds.), Use of proxies in paleoceanography: Examples from the South Atlantic, Springer-Verlag, Berlin (1999), pp. 601-633.]. Besides the detection and elimination of errors in single records, the stratigraphic network approach allows to check the intrinsic consistency of the final result by comparing it to the outcome of more restricted alignment procedures. The final South Atlantic stratigraphic network covers the last 400 kyr south and the last 1200 kyr north of the Subtropical Front (STF) and provides a highly precise age model across the STF representing extremely different sedimentary regimes. This allows to detect temporal shifts of the STF by mapping δMn / Fe. It turns out that the apparent STF movements by about 200 km are not directly related to marine oxygen isotope stages.  相似文献   

19.
Sm-Nd and Lu-Hf isotopic data are presented for 19 chondritic meteorites: six carbonaceous chondrites, five L-chondrites, seven H-chondrites, and a single enstatite chondrite. The primary goal of the study is to better define the Bulk Silicate Earth (BSE) reference values for Hf isotopes. Except for one sample with lower Sm/Nd, the Sm-Nd data define a cluster around the accepted reference values for chondrites and terrestrial planets, giving a mean 147Sm/144Nd of 0.1960±0.0005, and a mean 143Nd/144Nd of 0.512631±0.000010 (uncertainties are two standard errors). It seems appropriate to retain the presently accepted Sm-Nd reference parameters, 147Sm/144Nd=0.1966 and 143Nd/144Nd=0.512638 (when fractionation-corrected to 146Nd/144Nd=0.7219).Lu-Hf isotopic data are not clustered, but spread along an approximate 4.5-Ga isochron trend, with a range of 176Lu/177Hf from 0.0301 to 0.0354. The data are similar to many of the samples of chondrites presented by Bizzarro et al. [Nature 421 (2003) 931], but lack the range to lower Lu/Hf shown by those authors. Our chondrite data define a regression line of 4.44±0.34 Ga when 1.867×10−11 year−1 is used for the decay constant of 176Lu [Science 293 (2001) 683; Earth Planet. Sci. Lett. 219 (2004) 311-324]. Combining our data with the main population of analyses from Bizzarro et al. [Nature 421 (2003) 931] yields 4.51±0.24 Ga. Unless samples of eucrite meteorites and deviating replicates of chondrites with 176Lu/177Hf less than 0.030 are employed, no combination of the main population of chondrite Lu-Hf data yields a regression with sufficiently low error to constrain the decay constant of 176Lu. Sample heterogeneity seems to hinder the acquisition of reproducible Lu-Hf analyses from small, manually ground pieces of chondrites, and we suggest that analysis of powders prepared from large volumes of meteorite will be needed to adequately characterize the Lu-Hf isotope systematics of chondritic reservoirs and of BSE. Our results for carbonaceous chondrites show higher average 176Lu/177Hf and 176Hf/177Hf than ordinary chondrites, and the mean of carbonaceous chondrites also coincides with replicate analyses of a powder representing a large volume of meteorite, the Allende powder from the Smithsonian Institution. Use of the carbonaceous chondrite mean for BSE Lu-Hf characteristics results in a BSE Hf-Nd point that lies well within the array of terrestrial compositions, and leads to plausible initial εHf values for Precambrian rocks. An improved objective resolution of meteorite data and of meteoritic models for the Earth needs to occur before BSE can be established for Lu-Hf.  相似文献   

20.
We report small but significant variations in the 58Ni/61Ni-normalised 60Ni/61Ni and 62Ni/61Ni ratios (expressed as ε60Ni and ε62Ni) of bulk iron and chondritic meteorites. Carbonaceous chondrites have variable, positive ε62Ni (0.05 to 0.25), whereas ordinary chondrites have negative ε62Ni (− 0.04 to − 0.09). The Ni isotope compositions of iron meteorites overlap with those of chondrites, and define an array with negative slope in the ε60Ni versus ε62Ni diagram. The Ni isotope compositions of the volatile-depleted Group IVB irons are similar to those of the refractory CO, CV carbonaceous chondrites, whereas the other common magmatic iron groups have Ni isotope compositions similar to ordinary chondrites. Only enstatite chondrites have identical Ni isotope compositions to Earth and so appear to represent the most appropriate terrestrial building material. Differences in ε62Ni reflect distinct nucleosynthetic components in precursor solids that have been variably mixed, but some of the ε60Ni variability could reflect a radiogenic component from the decay of 60Fe. Comparison of the ε60Ni of iron and chondritic meteorites with the same ε62Ni allows us to place upper limits on the 60Fe/56Fe of planetesimals during core segregation. We estimate that carbonaceous chondrites had initial 60Fe/56Fe < 1 × 10− 7. Our data place less good constraints on initial 60Fe/56Fe ratios of ordinary chondrites but our results are not incompatible with values as high as 3 × 10− 7 as determined by in-situ measurements. We suggest that the Ni isotope variations and apparently heterogeneous initial 60Fe/56Fe results from physical sorting within the protosolar nebula of different phases (silicate, metal and sulphide) that carry different isotopic signatures.  相似文献   

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