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1.
An evaluation of the precision and resolution of the unspiked K–Ar dating method is presented with particular regard to the statistical significance of ages that are measured near or at the detection limit of the technique. Near-zero (historical) ages can be measured by the unspiked K–Ar technique with a precision that is essentially controlled by the precision with which the 40Ar/36Ar of the sample can be resolved from the present-day atmospheric value of 295.5. The best analytical precision on the isotopic ratio is ±0.05% (1σ) by this technique, which currently limits the lower detection limit of unspiked K–Ar ages to samples featuring at least 0.14% of radiogenic 40Ar. The corresponding youngest resolvable K–Ar age depends on the K content and atmospheric contamination of the sample. Total-fusion analysis of high-K refractory minerals like sanidine is not practicable via K–Ar, and the lowest resolvable age for medium-K samples more amenable to complete fusion is around 1.5 ka (on a single-run basis). It is argued that near-zero age measured with a probability density straddling or narrowing the time-origin cannot be handled without accounting for the non-negativity constraint imposed by the physical requirement of a positive age. The pertinent equations are derived both for the single-run case and for the case of independent replicates made on a single sample. We show that pooled K–Ar replicates can theoretically reduce the nominal uncertainty of individual unspiked ages (typically ±1.5 ka, 2σ) to a value that is close to the smallest 40Ar/39Ar isochron age uncertainty achievable on sanidine in the 0–2 ka range (±0.2 ka, 2σ). However, this performance is obtained at the cost of prohibitively large-sample statistics (n≥15) for medium-K feldspars datable via K–Ar. Coupled with the inability of the K–Ar approach to obviate the problems of excess/fractionated 40Ar and/or xenocrystic contamination, this makes the 40Ar/39Ar technique the method of choice for dating historical events by the K–Ar scheme.  相似文献   

2.
New U–Pb age-data from zircons separated from a Northland ophiolite gabbro yield a mean 206Pb/238U age of 31.6 ± 0.2 Ma, providing support for a recently determined 28.3 ± 0.2 Ma SHRIMP age of an associated plagiogranite and  29–26 Ma 40Ar/39Ar ages (n = 9) of basalts of the ophiolite. Elsewhere, Miocene arc-related calc-alkaline andesite dikes which intrude the ophiolitic rocks contain zircons which yield mean 206Pb/238U ages of 20.1 ± 0.2 and 19.8 ± 0.2 Ma. The ophiolite gabbro and the andesites both contain rare inherited zircons ranging from 122–104 Ma. The Early Cretaceous zircons in the arc andesites are interpreted as xenocrysts from the Mt. Camel basement terrane through which magmas of the Northland Miocene arc lavas erupted. The inherited zircons in the ophiolite gabbros suggest that a small fraction of this basement was introduced into the suboceanic mantle by subduction and mixed with mantle melts during ophiolite formation.

We postulate that the tholeiitic suite of the ophiolite represents the crustal segment of SSZ lithosphere (SSZL) generated in the southern South Fiji Basin (SFB) at a northeast-dipping subduction zone that was initiated at about 35 Ma. The subduction zone nucleated along a pre-existing transform boundary separating circa 45–20 Ma oceanic lithosphere to the north and west of the Northland Peninsula from nascent back arc basin lithosphere of the SFB. Construction of the SSZL propagated southward along the transform boundary as the SFB continued to unzip to the southeast. After subduction of a large portion of oceanic lithosphere by about 26 Ma and collision of the SSZL with New Zealand, compression between the Australian Plate and the Pacific Plate was taken up along a new southwest-dipping subduction zone behind the SSZL. Renewed volcanism began in the oceanic forearc at 25 Ma producing boninitic-like, SSZ and within-plate alkalic and calc-alkaline rocks. Rocks of these types temporally overlap ophiolite emplacement and subsequent Miocene continental arc construction.  相似文献   


3.
We report isotope analyses of helium, neon, argon, and xenon using different extraction techniques such as stepwise dynamic and static crushing, and high-resolution stepwise heating of three mantle xenoliths from Réunion Island. He and Ne isotopic compositions were similar to previously reported Réunion data, yielding a more radiogenic composition when compared to the Hawaiian or Icelandic mantle plume sources. We furthermore observed correlated 129Xe/130Xe and 136Xe/130Xe ratios following the mantle trend with maximum values of 6.93 ± 0.14 and 2.36 ± 0.06, respectively. High-resolution argon analyses resulted in maximum 40Ar/36Ar ratios of 9000–11,000, in agreement with maximum values obtained in previous studies. We observed a well-defined hyperbolic mixing curve between an atmospheric and a mantle component in a diagram of 40Ar/36Ar vs. 20Ne/22Ne. Using a mantle 20Ne/22Ne of 12.5 (Ne–B) a consistent 40Ar/36Ar value of 11,053 ± 220 in sample ILR 84-4 was obtained, whereas extrapolations to a higher mantle 20Ne/22Ne ratio of 13.8 (solar wind) would lead to a much higher 40Ar/36Ar ratio of 75,000, far above observed maximum values. This favours a mantle 20Ne/22Ne of about 12.5 considered to be equivalent to Ne–B. Extrapolated and estimated 40Ar/36Ar ratios of the Réunion, Iceland, Loihi, and MORB mantle sources, respectively, tend to be linearly correlated with air corrected 21Ne/22Ne and show the same systematic sequence of increasing relative contributions in radiogenic isotopes (Iceland–Loihi–Réunion–MORB) as observed for 4He/3He. In general, He–Ne–Ar isotope systematics of the oceanic mantle can be explained by following processes: (i) different degree of mixing between pure radiogenic and pure primordial isotopes generating the MORB and primitive plume (Loihi-type) endmembers; (ii) relatively recent fractionation of He relative to Ne and Ar, in one or both endmembers; (iii) after the primary fractionation event, different degrees of mixing between melts or fluids of MORB and primitive plume affinity generate the variety of observed OIB data, also on a local scale; (iv) very late-stage secondary fractionation during magma ascent and magma degassing leads to further strong variation in He/Ne and He/Ar ratios.  相似文献   

4.
We report the first measurements of hydrodynamic dispersion in a microfractured granite using a combination of novel techniques. A fracture network was induced in a cylindrical plug of Ailsa Craig micro-granite by thermal stressing, to produce an isotropic network of fractures with an average aperture of  0.3 μm, a density of approximately 4 × 104 fractures/mm3 and a permeability of 5.5 × 10− 17 m2. After saturating the cores with 0.01 M NaCl solution a step in the concentration profile to 1 M was advected into the plug at flow rates of 0.07 to 2.13 cm3 h− 1. The longitudinal electrical impedance of the plug was measured continuously as the solute front advected through its length until the plug was saturated with the concentrated electrolyte. Analysis of the impedance versus time relationships allows the derivation of the longitudinal dispersion coefficient, DL, and hydrodynamic retardation, RH. The Peclet number–dispersion relationship for the micro-fracture network is very similar to that predicted for other, radically different, fracture networks. Thus dispersion may be more dependent on fracture connectivity and length than fracture density and display a relationship similar to that shown by particle beds and clastic sandstones. The high retardation values observed (2.2–4.9) reflect flow behaviour within a fracture network with a proportion of ‘blind’ sections, and demonstrates how such networks can slow the advance of conservative solute components.  相似文献   

5.
We have considered the influence of ocean temperature and salinity changes, mass changes of the Greenland ice sheet (GIS) and the isostatic response of the solid earth to the most recent glacial cycle on 20th century sea-level change along the US east coast with the intention of better understanding the observed signal as well as determining the potential of the tide gauge data for constraining the recent (past 50–100 yr) mass balance of the GIS and earth viscosity structure. Our results show that the signal due to steric changes is large and displays a complex spatial variation which can account for a significant portion of the observed signal. In contrast, that due to changes in the GIS is relatively small and insensitive to the specific geometry of the mass balance model adopted. As a consequence, the tide gauge data alone are not capable of providing useful constraints on either the magnitude or form of recent GIS mass balance. Our inference of mantle viscosity structure based on the tide gauge data was affected dramatically when the steric effect was accounted for: An earth model with an upper mantle viscosity of 8 × 1019 Pa s and a lower mantle viscosity of 5 × 1022 Pa s produced the best fit to the steric-corrected data; the optimal fit to the uncorrected data was obtained for upper and lower mantle viscosities of 5 × 1020 Pa s and 1022 Pa s, respectively.  相似文献   

6.
186Os enrichments in volcanic rocks and peridotite-derived iridosmine grains have been attributed to contributions from Earth’s outer core to the mantle, and apparently constrain the scale of mantle convection and an early timing for inner–outer core segregation more than 3.5 Gyr ago. Here, we highlight that marine ferromanganese crusts and nodules are characterised by high Pt/Os ratios and Pt–Os contents that develop much larger 186Os excesses over geological time (≥0.2%/Gyr) than those hypothesised for Earth’s outer core (<0.005–0.01%/Gyr). 187Os/188Os ratios in ferromanganese crusts are radiogenic due to sequestering of continental Os from seawater. Similarly, ancient ferromanganese materials may have had 186Os excesses (>0.1%) as a result of high Pt/Os ratios in continental crust, even prior to in-growth of 186Os after formation due to their high Pt/Os ratios. Past recycling of small amounts of these materials into the Earth’s mantle will produce coupled 187Os–186Os excesses and little change in Re and platinum-group-element concentrations, as observed in Hawaiian picrites, and in contrast to the predicted result of outer core addition to the mantle. 187Os and 186Os enrichments in the Hawaiian mantle source are potentially consistent with it comprising recycled oceanic lithosphere, pelagic sediments and ferromanganese materials, and questions the notion that Os isotopes can be used to uniquely identify core–mantle interactions and the depth at which mantle sources for volcanism originate.  相似文献   

7.
We present Re–Os, Sm–Nd and Pb–Pb isotope and trace element data for the Konchozero sill, a layered mafic–ultramafic intrusion in the Early Proterozoic Onega plateau, one of the oldest continental flood basalt provinces on Earth. The Sm–Nd and Pb–Pb combined mineral and whole-rock isochron ages of 1988±34 and 1985±57 Ma for the sill coincide with the age of ferropicrites from Pechenga (the Kola Peninsula). The lithostratigraphic, chemical and isotope evidence suggest the derivation of Pechenga lavas and the Onega plateau volcanics from a single mantle plume. Peridotite and gabbro whole-rock samples, and primary ulvospinel and ilmenite mineral separates from the sill yield a Re–Os isochron with a slope corresponding to an age of 1969±18 Ma, γOs(T) =−0.61±5.9. This age is consistent with the other isotope data, and indicates the closed-system behavior of Re and Os in the rocks. The peridotites and ulvospinel have high Os concentrations (2.5–14 ppb) and low 187Re/188Os ratios (0.35–1.1), thus allowing a more accurate determination of the weighted average initial 187Os/188Os of 0.1144±0.0019 (2σpop), γOs(T) =+0.77±1.7. This value is lower than that determined by Walker et al. (Geochim. Cosmochim. Acta 61 (1997) 3145–3160) for the Pechenga lavas (γOs(T) =+6.1±0.7), and implies a substantial Os-isotope heterogeneity in this ancient plume. Compared to the Onega plateau primary basalt magma, Pechenga ferropicrites are relatively enriched in iron and Ni, have lower (Nb/Th)N ratios (2.1 vs 1.1) and less radiogenic Nd-isotope compositions (Nd(T) = +3.1 and +1.4, respectively), but share similar low-radiogenic Pb-isotope characteristics (μ1=8.57 and 8.60). Incorporation of small amounts (1.5%) of outer core material into the hotter central part of the plume and subsequent contamination of the Pechenga ferropicritic magmas with the 2.9 Ga Belomorian gneisses can explain the observed chemical and isotope variations in the two provinces provided that the core had <0.25 ppm of Pb.  相似文献   

8.
The East Asian monsoon Holocene optimal period has been debated both about duration and whether conditions were a maximum in thermal conditions or in precipitation. In this study we show Holocene climate variability inferred by a forest reconstruction of a subalpine pollen sequence from peat bog deposits in central Taiwan, based on modern analogues of various altitudinal biomes in the region. A warmer interval occurred between 8 and 4 ka BP (calibrated 14C years) when the subtropical forests were more extensive. The Holocene thermal optimum is represented by an altitudinal tropical forest at 6.1–5.9 ka BP and 6.9 ka BP and only the latter was accompanied by wet conditions, indicating decoupling of thermal and precipitation mechanism in the middle Holocene. Abrupt and relative severe cold phases, shown by biome changes, occurred at about 11.2–11.0 ka BP; 7.5 ka BP; 7.2 ka BP; 7.1 ka BP; 5.2 ka BP, 5.0 ka BP and 4.9 ka BP. A spectral analysis of pollen of a relatively cold taxon — Salix, reveals that the time series is dominated by a 1500 yr periodicity and similar to the cold cycle reported in the marine records of Indian and western Pacific Oceans. The cold–warm conditions inferred by the change of forests show close relationship to solar energy in comparison with the production rate of Be-10.  相似文献   

9.
Magma degassing at Soufrière Hills Volcano (SHV) is characterised by an almost permanent SO2 flux and a HCl production rate which mainly depends on dome growth rate. Degassing processes have been studied through textural, H2O and halogen analyses of clasts collected between 1995 and 2006 on the dome and in pyroclastic flows and vulcanian eruption deposits. Cl, Br and I are strongly depleted in melts during H2O degassing with no significant Cl–Br–I fractionation, whereas F is almost unaffected. All magmas erupted at SHV have followed a multi-step degassing path from the magma chamber up to a shallow depth ( 1 km, P  20 MPa). From that depth, however, effusive and explosive paths are distinct; vulcanian eruptions are the result of closed system degassing (CSD), while effusive dome growth is the result of CSD up to a very shallow depth (≤ 200 m, P  5–2 MPa) followed by open system degassing (OSD). CSD is modelled using the H2O solubility law, the perfect gas law and partition coefficients of halogens between a rhyolitic melt and H2O vapour (dv − li). Gas loss characteristic of OSD is modelled using a Rayleigh law. Degassing induced crystallisation is introduced through the ratio of crystallisation and degassing rates, which ranges from 150–500. dv − lCl for OSD ranges between 50–300, increasing with melt Cl content. For CSD, the lower effective dv − lCl ( 20) is attributed to kinetic effects.

Dome forming activity has a greater impact on atmospheric chemistry than vulcanian eruptions because OSD is much more efficient at extracting halogens. The model shows that HCl flux is a good proxy for the dome forming eruption rate. Comparison between model and measured gas compositions suggests a high HBr–BrO conversion rate (BrO/Total Br  1/3) in the SHV gas plume.

The degassing behaviour of Cl, Br and I implies similar Cl/Br ( 160) and Br/I ( 90) in initial melts, volcanic clasts and high temperature gases. The low Cl/Br at SHV compared to other island arcs ( 250–300) is attributed to a shallow, pre-eruptive Br enrichment. The almost permanent dome extrusion at SHV since 1995 has likely had a significant regional atmospheric impact because of the very efficient effusive degassing and the high conversion rate of halogens into reactive species within the gas plume.  相似文献   


10.
Re–Os isotope compositions of syngenetic sulphide inclusions in both eclogite suite (E-type) and peridotite suite (P-type) parageneses in diamonds from the Koffiefontein mine, South Africa have been analysed using a technique capable of analysing single inclusion grains, or, in some cases multiple inclusions from the same diamonds. Sulphide inclusion Ni contents broadly correlate with Os abundances in that low-Ni (6.8–8.7% Ni), E-type sulphides have 4.7 to 189 ppb Os whereas the two high-Ni (25%), P-type sulphides have 5986 and 6097 ppb Os. Two P-type sulphides from the same diamond define the first mineral isochron obtained for a single diamond which has an age of 69±30 Ma with chondritic initial 187Os/188Os. This indicates that the sulphides, and hence the host diamond, crystallised close to the time of kimberlite emplacement (90 Ma), in the Mesozoic. This is supported by Pb isotopic measurements of a fragment from one of the sulphides, together with the absence of significant Type IaB nitrogen aggregation in the host diamond lattice. E-type sulphide inclusions have radiogenic Os isotopic compositions, 187Os/188Os 0.346 to 2.28, and Re–Os model ages from 1.1 to 2.9 Ga. They define an array on a Re–Os isochron diagram that may be interpreted as defining a single period of E-type sulphide growth at 1.05±0.12 Ga, with an elevated initial 187Os/188Os. Alternatively, two episodes of sulphide crystallisation, from a chondritic reservoir, may be invoked in the Archaean and in the Proterozoic. The results for both P- and E-type diamonds point to a spectrum of diamond crystallisation ages. High contents of both Re and Os, and the similarity of Re/Os ratios of sulphide inclusions in diamonds to whole rock eclogite and peridotite xenoliths indicate that small amounts of sulphides can dominate the mantle budget of both these elements during melting. Recent addition to the lithospheric mantle of high-Os material similar to that from which the P-type sulphides crystallised may explain the variable, sometimes young Os model ages seen in whole rock xenolith Re–Os data.  相似文献   

11.
New noble gas data of ultramafic xenoliths from Réunion Island, Indian Ocean, further constrain the characteristics of primordial and radiogenic noble gases in Earth’s mantle plume reservoirs. The mantle source excess of nucleogenic 21Ne is significantly higher than for the Hawaiian and Icelandic plume reservoirs, similar to excess of radiogenic 4He. 40Ar/36Ar of the Réunion mantle source can be constrained to range between 8000 and 12 000, significant 129Xe and fission Xe excess are present. Regarding the relative contribution of primordial and radiogenic rare gas nuclides, the Réunion mantle source is intermediate between Loihi- and MORB-type reservoirs. This confirms the compositional diversity of plume sources recognized in other radioisotope systematics. Another major result of this study is the identification of the same basic primordial component previously found for the Hawaiian and Icelandic mantle plumes and the MORB reservoir. It is a hybrid of solar-type He and Ne, and ‘atmosphere-like’ or ‘planetary’ Ar, Kr, Xe (Science 288 (2000) 1036). 20Ne/22Ne ratios extend to maximum values close to 12.5 (Ne-B), which is the typical signature of solar neon implanted as solar corpuscular radiation. This suggests that Earth’s solar-type noble gas inventory was acquired by small (less than km-sized) precursor planetesimals that were irradiated by an active early sun in the accretion disk after nebular gas dissipation, or, alternatively, that planetesimals incorporated constituents irradiated in transparent regions of the solar nebula. Previously, such an early irradiation scenario was suggested for carbonaceous chondrites which follow common volatile depletion trends in the sequence CI–CM–CV–Earth. In turn, CV chondrites closely match Earth’s mantle composition in 20Ne/22Ne, 36Ar/22Ne and 36Ar/38Ar. This indicates that mantle Ar could well be a planetary component inherited from precursor planetesimals. However, a corresponding conclusion for mantle Kr and Xe is less convincing yet, but this may be just due to the lack of appropriate ‘meteoritic’ building blocks matching terrestrial composition. Alternatively, heavy noble gases in Earth’s mantle could be due to admixing of severely fractionated air, but this effect must have affected all mantle sources to a very similar extent, e.g. by global subduction before the last homogenization of the mantle reservoirs.  相似文献   

12.
In an attempt to constrain the origin of polycrystalline diamond, combined analyses of rare gases and carbon and nitrogen isotopes were performed on six such diamonds from Orapa (Botswana). Helium shows radiogenic isotopic ratios of R/Ra = 0.14–1.29, while the neon ratios (21Ne/22Ne of up to 0.0534) reflect a component from mantle, nucleogenic and atmospheric sources. 40Ar/36Ar ratios of between 477 and 6056 are consistent with this interpretation. The (129Xe/130Xe) isotopic ratios range between 6.54 and 6.91 and the lower values indicate an atmospheric component. The He, Ne, Ar and Xe isotopic compositions and the Xe isotopic pattern are clear evidence for a mantle component rather than a crustal one in the source of the polycrystalline diamonds from Orapa. The δ13C and δ15N isotopic values of − 1.04 to − 9.79‰ and + 4.5 to + 15.5‰ respectively, lie within the range of values obtained from the monocrystalline diamonds at that mine. Additionally, this work reveals that polycrystalline diamonds may not be the most appropriate samples to study if the aim is to consider the compositional evolution of rare gases through time. Our data shows that after crystallization, the polycrystalline diamonds undergo both gas loss (that is more significant for the lighter rare gases such as He and Ne) and secondary processes (such as radiogenic, nucleogenic and fissiogenic, as well as atmospheric contamination). Finally, if polycrystalline diamonds sampled an old mantle (1–3.2 Ga), the determined Xe isotopic signatures, which are similar to present MORB mantle – no fissiogenic Xe from fission of 238U being detectable – imply either that Xe isotopic ratios have not evolved within the convective mantle since diamond crystallization, or that these diamonds are actually much younger.  相似文献   

13.
We present new 40Ar/39Ar ages and paleomagnetic data for São Miguel island, Azores. Paleomagnetic samples were obtained for 34 flows and one dike; successful mean paleomagnetic directions were obtained for 28 of these 35 sites. 40Ar/39Ar age determinations on 12 flows from the Nordeste complex were attempted successfully: ages obtained are between 0.78 Ma and 0.88 Ma, in contrast to published K–Ar ages of 1 Ma to 4 Ma. Our radiometric ages are consistent with the reverse polarity paleomagnetic field directions, and indicate that the entire exposed part of the Nordeste complex is of a late Matuyama age. The duration of volcanism across São Miguel is significantly less than previously believed, which has important implications for regional melt generation processes, and temporal sampling of the geomagnetic field. Observed stable isotope and trace element trends across the island can be explained, at least in part, by communication between different magma source regions at depth. The 40Ar/39Ar ages indicate that our normal polarity paleomagnetic data sample at least 0.1 Myr (0–0.1 Ma) and up to 0.78 Myr (0–0.78 Ma) of paleosecular variation and our reverse polarity data sample approximately 0.1 Myr (0.78–0.88 Ma) of paleosecular variation. Our results demonstrate that precise radiometric dating of numerous flows sampled is essential to accurate inferences of long-term geomagnetic field behavior. Negative inclination anomalies are observed for both the normal and reverse polarity time-averaged field. Within the data uncertainties, normal and reverse polarity field directions are antipodal, but the reverse polarity field shows a significant deviation from a geocentric axial dipole direction.  相似文献   

14.
The new data presented here from a 10–24°N segment of the North Mid-Atlantic Ridge show that this segment is the most depleted of the 10–70°N ridge section. They also show the existence of: (1) a geochemical gradient from the 14°N anomaly to 17°10′N; (2) a very depleted mantle source (the lowest Sr isotopic ratios found so far in the North Atlantic); and (3) a geochemical limit located at about 17°10′N without any obvious relation with any structural feature. The 15°20′N fracture zone does not show any relationship with respect to this gradient. The basalts located north of 17°10′N have very homogeneous features, which allow their characteristics to be averaged (i.e., 87Sr/86Sr= 0.70238 ± 0.00004, (Nb/Zr)N = 0.28 ± 0.1) and they are defined as normal mid-ocean ridge basalts. The basaltic glasses located south of 17°10′N present a wide spectrum of isotopic compositions and extended rare earth element patterns (from depleted to enriched). Despite this, they have a constant K/Nb of 233 ± 9 (1sM, n = 18) whereas this ratio is 344 ± 29 north of 17°10′N. These observations illustrate the strong coherence of behaviour between K and Nb (Ta) during the petrogenic processes involved in the generation of these mid-ocean ridge basalts and also their fractionation during previous mantle processes. Possible interpretations of mixing processes are discussed and sources at the ridge segment scale are favoured. However, when looking in detail, local heterogeneities are still common and can even be traced back off-axis to 115 my.

Placed in the context of the North Atlantic Ridge from 10° to 70°N, the Sr isotopic ratios reveal the Azores superstructure (23–50°N), whereas the trace element ratios (La/Sm-Nb/Zr) trace the second-order structures (33–40°N, 42–48°N) superimposed on the superstructure. This study illustrates the complementarity of information given by certain well chosen trace element ratios on the one hand and by isotopic ratios on the other. Since there is evidence of decoupling between isotopic ratios and/or trace element ratios, it introduces the notion of complementary “chemical memory” as recorded by a given type of trace element ratio or a given type of isotopic ratio  相似文献   


15.
The timing of ultra-high pressure (UHP) metamorphism has been difficult to determine because of a lack of age constraints on crucial events, especially those occurring on the prograde path. New Sensitive High-Resolution Ion Microprobe (SHRIMP) U–Pb age and rare-earth element (REE) data of zircon are presented for UHP metamorphic rocks (eclogite, garnet peridotite, garnet pyroxenite, jadeite quartzite and garnet gneiss) along the Dabie–Sulu UHP complex of China. With multiphase metamorphic textures and index mineral inclusions within zircon, the Dabie data define three episodes of eclogite-facies metamorphism, best estimated at 242.1 ± 0.4 Ma, 227.2 ± 0.8 Ma and 219.8 ± 0.8 Ma. Eclogite-facies zircons of the Sulu UHP complex grew during two major episodes at 242.7 ± 1.2 and 227.5 ± 1.3 Ma, which are indistinguishable from corresponding events in the Dabie UHP complex. A pre-eclogite metamorphic phase at 244.0 ± 2.6 Ma was obtained from two Sulu zircon samples which contain low pressure–temperature (plagioclase, stable below the quartz/Ab transformation) and hydrous (e.g., amphibole, stable below  2.5 Gpa) mineral inclusions. In terms of Fe–Mg exchange of trapped garnet–clinopyroxene pairs within zircon domains, we are able to determine the Pressure–Temperature (PT) conditions for a specific episode of metamorphic zircon growth. We suggest that mineral phase transformations and associated dehydration led to episodic eclogite-facies zircon growth during UHP metamorphism ( 2.7 Gpa) began at 242.2 ± 0.4 Ma (n = 74, pooling the Dabie–Sulu data), followed by peak UHP metamorphism (>  4 Gpa) at 227.3 ± 0.7 Ma (n = 72), before exhumation (<  220 Ma) to quartz stability (~ 1.8 Gpa). The Dabie–Sulu UHP metamorphism lasted for about 15 Ma, equivalent to a minimum subduction rate of 6 mm/year for the descending continental crust.  相似文献   

16.
A phase transition in pure CaSiO3 perovskite was investigated at 27 to 72 GPa and 300 to 819 K by in-situ X-ray diffraction experiments in an externally-heated diamond-anvil cell. The results show that CaSiO3 perovskite takes a tetragonal form at 300 K and undergoes phase transition to a cubic structure above 490–580 K in a pressure range studied here. The transition boundary is strongly temperature-dependent with a slightly positive dT / dP slope of 1.1 (± 1.3) K/GPa. It is known that the transition temperature depends on Al2O3 content dissolved in CaSiO3 perovskite [Kurashina et al., Phys. Earth Planet. Inter. 145 (2004) 67–74]. The phase transition in CaSiO3(+ 3 wt.% Al2O3) perovskite therefore could occur in a cold subducted mid-oceanic ridge basalt (MORB) crust at about 1200 K in the upper- to mid-lower mantle. This phase transition is possibly ferroelastic-type and may cause large seismic anomalies in a wide depth range.  相似文献   

17.
Granoblastic olivine aggregates (GOA) have been discovered in some Type I magnesian chondrules within carbonaceous chondrites by Libourel and Krot [Libourel, G., Krot, A.N., 2007. Evidence for the presence of planetesimal material among the precursors of magnesian chondrules of nebular origin. Earth Planet. Sci. Lett. 254, 1–8], who proposed an origin from pre-existing planetesimals. Amoeboid olivine aggregates (AOA), generally considered as aggregates of solar nebula condensates and found within similar carbonaceous chondrites, display similar equilibrium texture, though on a finer scale. For these reasons, we conducted experiments to determine if annealing of olivine required time scales appropriate to planetesimal or nebular heating. Pressed < 43 µm and < 63 µm San Carlos olivine powder (Fo88.4) was isothermally heated at temperatures ranging from 1350–1550 °C for 1–100 h. The 100 h runs yield olivine aggregates with well-developed granoblastic texture at all temperatures, manifest as a network of randomly-oriented and sutured olivine grains with 120° triple junctions. Individual olivine grains are 4–6 sided and polygonal by 1450 °C and equigranular texture is developed at high temperature (1500–1550 °C). Melting of olivine commences at 1450–1500 °C and aids in ‘ripening’ and suturing (grain coarsening and grain boundary migration). Textural equilibrium is clearly met at 1550 °C. A planetesimal origin cannot be ruled out; however, the experimental evidence reveals that granoblastic texture can be reproduced in an interval not inconsistent with heating times for nebular objects. GOA may have experienced higher degrees of thermal processing than the finer-grained AOA. If the precursors were the same, grain coarsening would have to be accompanied by modification to bulk and isotopic compositions. However, the precursors could have been olivine condensates formed later than AOA. Annealing may have been a widespread process operating in the primordial solar nebula responsible for thermal processing and formation of GOA prior to their incorporation into chondrules.  相似文献   

18.
Benthic foraminiferal magnesium/calcium ratios were determined on one hundred and forty core-top samples from the Atlantic Ocean, the Norwegian Sea, the Indian Ocean, the Arabian Sea and the Pacific Ocean, mostly at sites with bottom water temperatures below 5 °C. Mg/Ca ratios are consistently lower, by  0.2 mmol/mol, in samples cleaned using oxidative and reductive steps than using oxidative cleaning. Differences between Cibicidoides species have been identified: Mg/Ca of Cibicidoides robertsonianus > Cibicidoides kullenbergi > Cibicidoides wuellerstorfi. Comparison with bottom water temperatures support observations of lowered Mg/Ca of C. wuellerstorfi at temperature below  3 °C compared with values predicted by published calibrations and from other Cibicidoides species. Hydrographic data shows that carbonate ion saturation (Δ[CO32−]) decreases rapidly below this temperature. An empirical sensitivity of Δ[CO32−] on Mg/Ca has been established for C. wuellerstorfi of 0.0086 ± 0.0006 mmol/mol/μmol/kg. A novel application using modern temperatures and Last Glacial Maximum temperatures derived via pore fluid modelling supports a carbonate ion saturation state effect on Mg incorporation. This may significantly affect calculated δ18Oseawater obtained from foraminiferal δ18O and Mg/Ca temperature.  相似文献   

19.
The igneous rocks of the Pongola Supergroup (PS) and Usushwana Intrusive Suite (UIS) represent a case of late Archaean continental magmatism in the southeastern part of the Kaapvaal craton of South Africa and Swaziland.

U-Pb dating on zircons from felsic volcanic rocks of the PS yields a concordia intercept age of 2940 ± 22Ma that is consistent with a Sm-Nd whole rock age of 2934 ± 114Ma determined on the PS basalt-rhyolite suite. The initial εNd of−2.6 ± 0.9 is the lowest value so far reported for Archaean mantle-derived rocks. Rb-Sr whole rock dating of the PS yields a younger isochron age of 2883 ± 69Ma, which is not significantly different form the accepted U-Pb zircon age.

An internal (cpx-opx-plag-whole rock) isochron for a pyroxenite from the younger UIS yields an age of 2871 ± 30 Ma and initial 143Nd/144Nd that lies off the CHUR growth curve by εNd −2.9 ± 0.2. However, Sm-Nd whole-rock data for the UIS yield an excessively high age of 3.1 Ga that conflicts with firm geological evidence showing the UIS to be intrusive into the PS.

The negative deviations of initialεNd from the chondritic Nd evolution curve suggest significant contamination of the PS and UIS melts by older continental crust. A mixing process with continental crust after magma segregation is supported by a high initial 87Sr/86Sr ratio of0.703024 ± 24 for a clinopyroxene sample from a UIS pyroxenite, compared with an expected value of 0.701 for the 2.9 Ga mantle. We therefore interpret the linear array of data points for the UIS gabbros as a mixing line between 2.87 Ga old magma and older continental crust.

Parallel LREE-enriched REE patterns, negative Nb-Ti anomalies, a distinctive and uniform ratio of Ti/Zr 46 and a narrow span of initial Nd indicate a common source for both the PS and UIS suites which is different from primitive mantle.  相似文献   


20.
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   

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